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ICRU REPORT 57
ICRU REPORT 57

Conversion Coefficients for


use in Radiological Protection

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Against External Radiation

Issued: 1 August 1998

INTERNATIONAL COMMISSION ON RADIATION


UNITS AND MEASUREMENTS
7910 WOODMONT AVENUE
BETHESDA, MARYLAND 20814
U.S.A.
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Copyright ~ 1997 ICRP and ICRU


All rights reserved.

(For detailed information on the availability of this and other ICRU Reports, see page 129.)
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Contents ~
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Foreword ................ .. ......... . ............. .. ......... . v


Preface ..... . . . .................................. ... ......... . vii
Glossary of Terms and Definitions of Quantities . ... ... . .... . . IX

1. Introduction . .................................. .. ......... . 1


2. Quantities Used in Radiological Protection for External
Radiation ........... .. ........ . . .. ........ . .. ... ....... . . 3
2.1 Introduction .. .... . . .... . . .. .. . .... ....... . .......... . .. . 3
2.2 The Evolution of Quantities for Radiological Protection
against External Radiation ..... . ............. . ........ . 3
2.2.1 General .................. . .......... . ........... . 3
2.2.2 Dose equivalent ........... . ..................... . 3

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2.2.3 The maximum dose equivalent (MADE) ............ . 4
2.2.4 Conversion coefficients ..... ... .... .. .. . ... . . ... . . . 4
2.2.5 Dose equivalent indexes ... . . . ...... .. . . ...... . . . . . 4
2.2.6 Effective dose equivalent . ............. .. ......... . 5
2.2.7 Operational quantities ..... . ........ . ............ . 5
2.2.8 ICRP Publication 51 ..... . .. . ........ . ......... .. . 5
2.2.9 The Paris Statement of the ICRP (ICRP, 1985) ..... . . 5
2.2.10 ICRU Report 40 (ICRU, 1986) ...... . .. .... ....... . . 5
2.2.11 ICRP Publication 60 ................... . ......... . 5
2.2.12 ICRU Reports 47 and 51. ... ............ . ......... . 6
2.2.13 Summary ... .... ....... ...... ....... . . ... ....... . 6
2.3 Absorbed Dose . ... . ..... ....... .... ...... .... .... . ..... . 6
2.3.1 Absorbed dose . .... ...... ... .. . .. . .. ... .. . . . ..... . 6
2.3.2 Absorbed dose distributions . . ....... ... . . ........ . 6
2.3.3 Mean absorbed dose ..... .. . . ......... ... ......... . 6
2.4 Radiation Weighting . .. ...... . . .. ......... .. ............ . 6
2.4.1 General ......... . .......... .. .. . ......... . .. . . .. . 6
2.4.2 Radiation weighting for protection quantities ... . .. . . 7
2.4.3 Radiation weighting factors for electrons
and photons ....................... .. .......... . 7
2.4.4 Radiation weighting factors for neutrons ........... . 7
2.4.5 Radiation weighting for operational quantities ..... . 7
2.4.6 Q(L) - L relationship . ..... . . ......... .. . . .... . .. . 7
2.4.7 Mean quality factor, Q . . .. .. . .......... .... ....... . 8
2.4.8 Stopping power .......... .. ........... .. ......... . 8
2.5 Radiological Protection Quantities ............ . .. . ....... . 9
2.5.1 General . . ... .... ...... ..... ......... .. ....... . .. . 9
2.5.2 Organ absorbed dose ......... .. .. ... ..... ... .. . .. . 9
2.5.3 Equivalent dose .. .. . .. . . .... . ... ... ..... . . ... . .. . 9
2.5.4 Effective dose .. . ................................. . 9
00
2.6 Operational Quantities ....................... .. ......... . 10 m
m
2.6.1 General .............. . ..... . .................... . 10 ....
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2.6.2 Dose equivalent . .. .... .. .. . . ... .... .. ........... . 10 lQ

1::
2.6.3 Operational quantities for area monitoring . . ....... . 10 0
0-
2.6.4 Operational quantities for individual monitoring ... . 11 ~
;:J
3. Determination of Absorbed Dose Distributions in The p::
Human Body and in Anthropomorphic 8
and Other Models . . .. ........ . . . .... .. ..... . . .. . .. ...... . 13
3.1 Introduction .. .. .. .... ... . .. ....... . ... . ...... .. . . ... .. . . 13
3.2 Radiation Field ... .. . . ............. . ....... . . . . . ....... . . 13
3.3 Models and Phantoms of the Human Body .... .. . . ........ . 15 iii
Q
.S 3.3.1 Reference man................................... 15
...,
3.3.2 Simple phantoms. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 15
:e'" 3.3.3 Anthropomorphic models. . . . . . . . . . . . . . . . . . . . . . . . .. 15
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'" 3.4 Methods of Calculating Absorbed Dose Distributions. . . . . . .. 16
6 3.4.1 Introduction...................................... 16
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3.4.2 Transport codes: general features and special codes .. 17
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3.5 Irradiation Geometries. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ..
3.5.1 General..........................................
20
20
'0;
~ 3.5.2 Geometries used with the ICRU sphere. .. .. .. . . . . .. 21
Q
0
3.5.3 Geometries used with the ICRU slab. . . . .. .. . .. . . . .. 21
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4. Conversion Coefficients. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 22
0
&: 4.1 Introduction............................................. 22
"; 4.2 General....... . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 22
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4.2.1 Radiation energy spectra and mixed radiation fields.. 22
'0 4.3 Conversion Coefficients for Photons ....................... 22
:e 4.3.1 Introduction...................................... 22
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.S 4.3.2 Special considerations for photons. . . . . . . . . . . . . . . . .. 23
Q)
rn 4.3.3 Methods of calculation ............................ 23
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4.3.4 Available data. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 25
<2 4.3.5 Conversion coefficients and analysis. . . . . . . . . . . . . . .. 27
...,rn
Q 4.4 Conversion Coefficients for Neutrons. .. . . . . .. . . . . . . . .. . . .. 34
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4.4.1 Introduction...................................... 34
IEQ)
0 4.4.2 Special considerations for neutrons. . . . . . . . . . . . . . . .. 34
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Q 4.4.3 Methods of calculation ............................ 35
.S 4.4.4 Available data. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 36
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> 4.4.5 Conversion coefficients and analysis:
Q
0 protection quantities. . . . . . . . . . . . . . . . . . . . . . . . . . . .. 39
U
4.5 Conversion Coefficients for Electrons. . . . . . . . . . . . . . . . . . . . .. 46
4.5.1 Introduction...................................... 46
4.5.2 Special considerations for electrons. . . . . . . . . . . . . . . .. 46
4.5.3 Methods of calculation ............................ 47
4.5.4 Available data. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 49
4.5.5 Conversion coefficients and analysis:
protection quantities. . . . . . . . . . . . . . . . . . . . . . . . . . . .. 49
5. Relationships Between Quantities ........................ 57
5.1 Introduction............................................. 57
5.2 Changes in the Protection and Operational Quantities . . . . .. 57
5.2.1 General.......................................... 57
5.2.2 Protection quantities. . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 57
5.2.3 Operational quantities . . . . . . . . . . . . . . . . . . . . . . . . . . .. 62
5.3 Relationships between the Protection and Operational
Quantities: The Performance ofthe Operational
Quantities. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 64
5.3.1 General.......................................... 64
5.3.2 Area monitoring. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 66
5.3.3 Individual monitoring. . . . . . . . . . . . . . . . . . . . . . . . . . . .. 68
5.3.4 Summary ........................................ 76
5.4 General Conclusions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 77
ANNEXES-Introduction. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 78
ANNEX 1. FIGURES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 81
ANNEX 2. TABLES ............................................ 105
REFERENCES . ............................................... 122
ICRU Reports ................................................ 129

iv Index ......................................................... 133


Fore\Vord
Following the 1977 Recommendations ofthe Inter- determining whether the operational quantities still
national Commission on Radiological Protection represent adequately the protection quantities. The
(ICRP), the International Commission on Radiation conclusion is that, with some exceptions that are not
Units and Measurements (ICRU) developed a set of of significance for radiological protection, the opera-
measurable operational quantities to supplement tional quantities continue to achieve their objective.
those dosimetric quantities that are specified in the The report provides an extensive and authoritative
human body by the ICRP, sometimes called protec- set of data linking field quantities, operational quanti-
tion quantities. The 1990 ICRP Recommendations ties and protection quantities in a way that will be of
made some changes to the specification of these help to those working in radiological protection.
protection quantities. It was agreed that the final report, which has been
As a result, a Joint Task Group of the ICRP and approved by both Commissions, would be published
the ICRU was established with the principal aim of in the Annals of the ICRP and as an ICRU Report.

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v
Preface
This report was prepared by a Joint Task Group of The ICRU Sponsors ofthe report were:
the International Commission on Radiological Protec- R. S. Caswell
tion (lCRP) and the International Commission on P. M. DeLuca
Radiation Units and Measurements (lCRU). The
terms of reference of the Joint Task Group are Members of the International Commission on Ra-
discussed in the Introduction (Section 1). diological Protection during the preparation of this
The Joint Task Group had the following member- report:
ship: R. H. Clarke (Chairman) A. Kaul
Full Members C. B. Meinhold D. Li
R. H. Thomas (Chairman) G. Dietze (Vice-Chairman) J. Liniecki
L.VV.Brackenbush G. Drexler D. Beninson H. Matsudaira

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J-L. Chartier H. G. Menzel H. J. Dunster F. Mettler
M.J. Clark L.A. Ilyin vv. K. Sinclair
Corresponding Members vv. Jacobi H. Smith
R. Griffith B. R. L. Siebert H. P.Jammet (Scientific Secretary)
B. Grosswendt M. Zankl
N. Petoussi-Henss Members of the International Commission on Ra-
The membersip of ICRP Commitee 2 during the diation Units and Measurements during the prepara-
period of the Joint Task Group was: tion of this report:
A. Kaul F. A. Fry M. Roy A. Allisy (Chairman) M.Inokuti
(Chairman) J.Inaba J. vv. Stather A. VVambersie (Vice-Chairman) I. Isherwood
A. Bouville I. A. Likhtarev D. M. Taylor R. S. Caswell (Secretary) H. G. Menzel
X. Chen H. Metivier R. H. Thomas P. M. DeLuca H. G. Paretzke
F. T. Cross H. G. Paretzke K. Doi H. H. Rossi
G. Dietze A. R. Reddy L. Feinendegen G. F. VVhitmore
K. F. Eckerman vv. R. Ney (Assistant Secretary)

vii
Glossary of TerDlS and
Definitions of Quantities
Absorbed Dose Effective Dose
denoted as D, is the quotient of dE by dm, where dE a summation of the equivalent doses in tissues or
is the mean energy imparted by ionising radiation to organs, each multiplied by the appropriate tissue
matter of mass dm, thus weighting factor. It is given by the expression
dE E = ,LwT·HT
D=- T
dm
where HT is the equivalent dose in tissue or organ, T,
The unit of absorbed dose is joule per kilogram (J
and WT is the tissue weighting factor for tissue, T (see

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kg-I) and its special name is gray (Gy).
Table 3). The effective dose can also be expressed as
the sum of the doubly weighted absorbed dose in all
Ambient Dose Equivalent the tissues and organs of the body.
denoted as H*(d), at a point in a radiation field is
the dose equivalent that would be produced by the Effective Dose Equivalent
corresponding expanded and aligned field in the
denoted as HE, is the weighted average of the
ICRU sphere at a depth, d, on the radius opposing
mean dose equivalents, each weighted by a tissue or
the direction of the aligned field. The unit of ambient
organ weighting factor, thus:
dose equivalent is joule per kilogram (J kg-I) and its
special name is sievert (Sv). HE = ,LwTHT
T

Directional Dose Equivalent where HT is the mean dose equivalent in tissue, T,


and WT is the tissue weighting factor for tissue, T, as
denoted as H'(d,n), at a point in a radiation field, formerly recommended by the ICRP (see Table 1).
is the dose equivalent that would be produced by the
corresponding expanded field in the ICRU sphere at
depth, d, on a radius in a specified direction, D. The Energy Imparted
unit of directional dose equivalent is joule per kilo- denoted as E, by the ionising radiation to matter in
gram (J kg-I) and its special name is sievert (Sv). a volume is given by:
E = Rin - Rout + 2,Q
Dose Equivalent
where R in is the radiant energy incident on the
denoted as H, is the product of Q and D at a point volume, i.e., the sum of all the energies (excluding
in tissue, where D is the absorbed dose and Q is the rest energies) of all those charged and uncharged
quality factor at that point, thus ionising particles that enter the volume; Rout is the
H=QD. radiant energy emerging from the volume, i.e., the
sum of all the energies (excluding rest energies) of all
The unit of dose equivalent is joule per kilogram (J those charged and uncharged ionising particles that
kg-I) and its special name is sievert (Sv).

Dose Equivalent Indexl , HI TABLE 1. - Tissue weighting factors (ICRP Publication 26)a
maximum dose equivalent within the ICRU sphere Tissue or organ Tissue weighting factor, W'f
centered at the point in space to which the quantity
is assigned. The outer 0.07 mm thick shell is ignored. Gonads 0.25
Bone marrow (red) 0.12
It was also called the unrestricted dose equivalent Lung 0.12
index (see ICRU, 1980) (see also ICRU, 1988 for a Breast 0.15
definition of deep and shallow dose equivalent in- Thyroid 0.03
dex). Bone surfaces 0.03
Remainder 0.30
a ICRP (1977); see paragraph 105 of ICRP Publication 26 for
1 Obsolete quantity; included for completeness. further details of Remainder Tissues. ix
leave the volume; and IQ is the sum of all changes of Individual Dose Equivalent, penetrating,
the rest mass energy of nuclei and elementary Hp(d)
particles in any interactions that occur in the vol- the dose equivalent in soft tissue below a specified
ume. (In the sum, decreases are denoted by ( + ) and point on the body at depth, d , which is appropriate
increases are denoted by (- ).) The expectation value for strongly penetrating radiation.
of E, termed the mean energy imparted and denoted E,
is closely related to the definition of the absorbed
dose,D . Individual Dose Equivalent, superficial,
H.(d)

the dose equivalent in soft tissue below a specified


Equivalent Dose point on the body at a depth, d , which is appropriate
denoted as HT,R, is the absorbed dose in an organ or for weakly penetrating radiation (superseded by
tissue multiplied by the relevant radiation weight- personal dose equivalent).
ing factor (see Table 2), thus:
HT,R = WR • DT,R Kerma,K

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where DT,R is the absorbed dose averaged over the the quotient ofdEtr by dm , where dEt r is the sum of
tissue or organ, T, due to radiation R, and WR is the the initial kinetic energies of all the charged ionising
radiation weighting factor for radiation, R. When the particles liberated by uncharged ionising particles in
radiation field is composed of radiations with differ- a volume element of mass dm , thus:
ent values ofwR, the absorbed dose is subdivided into dE t r
blocks, each multiplied by its own value of W R and K=-
dm
summed to determine the total equivalent dose, i.e.,
The unit of kerma is joule per kilogram (J kg- I) and
HT = LWR . DT,R its special name is gray (Gy).
R

The unit of equivalent dose is joule per kilogram (J


kg- l) and its special name is sievert (Sv). Linear Energy Transfer
or linear collision stopping power, L, of a material,
for a charged particle, is the quotient of dE by dl,
Fluence where dE is the mean energy lost by the particle,
denoted as cP, is the quotient of dN by da , where owing to collisions with electrons, in traversing a
dN is the number of particles incident on a sphere of
distance dL, thus:
cross-sectional area da, thus:
dN
cP=-
da
Operational Quantity
a quantity with which, by means of its measure-
TABLE 2. - Values for radiation weighting factors (ICRP ment, compliance with the system of protection may
Publication 60)a
be demonstrated. Examples of operational quanti-
Radiation ties are ambient dose equivalent, directional dose
we ighting
Types and energy ra nge of radiation factor, WR
equivalent and personal dose equivalent.

Photons, all energies 1


Electrons and muons, all energies b 1 Organ Dose
Neutrons, energy
< 10keV 5 for radiation protection purposes. It is the mean
10-100 keV 10 absorbed dose, D T , in a specified tissue or organ of
> 100 keV to 2 MeV 20
> 2-20 MeV 10
the human body, T, given by
> 20 MeV 5
Protons , other than recoil protons, energy > 2 MeV 5 DT = (l/mT)imTDdm or E~mT
Alpha particles, fission fragments , heavy nuclei 20
a ICRP (1991a). where mT is the mass of tissue or organ, D is the
b Excluding Auger electrons emitted from nuclei bound to DNA, absorbed dose in the mass element dm, and €T is the
x for which special micr odosimetric considera tions are needed. total energy imparted in the tissue or organ.
Personal Dose Equivalent TABLE 3. - Tissue weighting factors a

Tissue or organ Tissue weighting factor,


denoted as Hp(d), is the dose equivalent in soft WT

tissue at an appropriate depth, d, below a specified Gonads 0.20


point on the body. The unit of personal dose equiva- Bone marrow (red) 0.12
lent is joule per kilogram (J kg-I) and its special Colon 0.12
Lung 0.12
name is sievert (Sv).
Stomach 0.12
Bladder 0.05
Breast 0.05
Protection Quantities
Liver 0.05
dosimetric quantities specified in the human body Oesophagus 0.05
Thyroid 0.05
by the ICRP. Examples of protection quantities are
Skin 0.01
effective dose and equivalent dose. Bone surface 0.01
Remainder 0.05

Quality Factor a See footnotes on Table 2 of ICRP Publication 60 for further


details.

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a function, Q, of unrestricted linear energy trans-
fer, L, in water. Values of Q(L) as a function of L are
given in ICRP Publication 60 (lCRP, 1991a) by the When calculation of the radiation weighting fac-
following relations: tors for neutrons requires a continuous function, the
Q(L) = 1 (L < 10) following approximation can be used:
Q(L) = 0.32L - 2.2 (10 :s; L :s; 100) -(In (2En»2]
wR = 5 + 17 exp [ 6
Q(L) = 300/~L (L> 100)
where L is expressed in keV /Lm -1. where En is the neutron energy in MeV. There is no
The mean quality factor, QT, in a specified tissue or intention to imply any biological meaning to this
organ, T, is given by relationship. It is simply a tool for calculation.
For radiation types and energy that are not in-
cluded in this table, an approximation of WR can
be obtained by calculation of Q at a depth of 10 mm
where DT is the mean absorbed dose to the tissue or in the ICRU sphere:
organ, mT is its mass, and Q and D are the quality
- f
factors and the absorbed dose in the mass element Q = 151 JLQ(L)D(L)dL
dm, respectively.
where D(L)dL is the absorbed dose at 10 mm be-
tween linear energy transfer, L, and L + dL; and
Relative Biological Effectiveness, RBEM
Q(L) is the quality factor at 10 mm [paragraphA14,
the ratio of the absorbed dose of a reference ICRP Publication 60 (ICRP, 1991a)].2
radiation to the absorbed dose of a given test radia-
tion required to produce the same level of response,
all other conditions being kept constant. The sub-
Tissue Weighting Factor, WT
script M refers to a stochastic effect. a factor by which the equivalent dose to a tissue or
organ is multiplied in order to account for the
relative stochastic detriment resulting from the expo-
Radiation Weighting Factor
sure of different tissues and organs. (See Table 3 for
A factor denoted WR, by which the tissue or organ the tissue weighting factors as now recommended by
absorbed dose is multiplied to reflect the higher ICRP.)
RBEM values for neutrons and alpha particles com-
pared with low LET radiations. Table 2 gives the
2 The symbol D(L) has historically been used by the ICRP for
values of radiation weighting factor used for radiologi- the absorbed dose between linear energy transfer, L, and L + dL.
cal protection purposes as now recommended by ICRU uses DL for the same quantity. In both instances the more
ICRP. usual mathematical symbol would be dD/dL.

xi
Conversion Coefficients for use
in Radiological Protection
Against External Radiation
1. Introduction

(1) This report summarises the work of a Joint operational quantities, if computed using a revised
Task Group on Dose-Related Quantities for Radiologi- Q(L) - L relationship given in ICRP Publication 60,
cal Protection against External Radiation estab- would be unlikely to underestimate the equivalent

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lished in the latter part of 1991. This group was dose. (The numerical specifications of the two Q(L) -
appointed by both the International Commission on L relationships in ICRP Publications 26 and 60 are
Radiological Protection (ICRP) and the Interna- different.) One of the important tasks of this report is
tional Commission on Radiation Units and Measure- to explain the implications and effects of all these
ments (ICRU). changes.
(2) In 1990, the ICRP approved new basic recom- (5) One ofthe principal objectives of the ICRU is to
mendations that replaced those of ICRP Publication develop internationally acceptable recommenda-
26 (ICRP, 1977) and those contained in Statements tions for quantities and units of radiation and radio-
supplementary to that publication (ICRP, 1978, 1980, activity in the radiation protection field. In this
1985). The new recommendations, which are pub- regard, the ICRU carries out its work in close
lished in ICRP Publication 60 (ICRP, 1991a), include cooperation with the ICRP.
new quantities for use in radiological protection. The (6) The charge 4 to the Joint Task Group was to
new quantities demand a review of much of the basic provide:
data used in the protection against exposure to • fluence to effective dose and effective dose-
sources of ionising radiations, both internal and equivalent calculations for a variety of radia-
external to the human body. This report is solely tions and energies for reference man and for
concerned with the implications for external expo- 15-year-old, 5-year-old, and 3-month-old chil-
sure. dren;
(3) As explained in some detail in Section 2, two • fluence to ambient dose equivalent, directional
sets of quantities are of importance in radiological dose equivalent, individual dose equivalent (pen-
protection. For example, dose limits are expressed in etrating), and individual dose-equivalent calcula-
terms of protection quantities and compliance with tions (superficial);5 and
these limits is demonstrated by a determination of • a detailed discussion of the relationship between
the appropriate operational quantity. the two sets of calculations.
(4) One particular aspect of the new ICRP recom- (7) The three principal protection quantities cur-
mendations is that they represent a significant depar- rently recommended for use in radiological protec-
ture from those in ICRP Publication 26 with respect tion are
to radiation weighting. ICRP Publication 26 pro- • the mean absorbed dose in an organ or tissue,
vided quality factors to account for differences in DT;
radiation quality. These quality factors were in- • the equivalent dose in an organ or tissue, H T ;
tended to facilitate the assessment of dose equiva- and
lent either by means of measurement or by calcula- • the effective dose, E.
tion using the Q(L) - L relationship.3 The ICRU (8) These quantities are defined in the Glossary
used (and still uses) quality factors in the definition and discussed in detail in Section 2. The protection
of the operational quantities. In contrast to the quantities are not directly measurable, but may be
recommendations of ICRP Publication 26, ICRP related by calculation to the radiation field in which
Publication 60 specifies the use of the radiation the exposure occurs. To form a bridge between the
weighting factors, WR, to derive protection quanti-
ties. The ICRP further suggested that the ICRU 4 The charge to the Joint Task Group was slightly different from
each Commission. This version combines both sets of charges.
5 In view of subsequent changes in nomenclature, this sentence
3 Throughout this report, for simplicity L is used to mean Loo, would now be written "fluence to ambient dose equivalent,
the linear energy transfer in water. directional dose equivalent, and personal dose equivalent". 1
protection quantities and the radiation field, the 1987) and JCRU Report 43 (ICRU, 1988), which gave
ICRU has developed operational quantities for mea- conversion coefficients for the dosimetric quantities
surement of exposures to external radiations. These previously recommended in JCRP Publication 26
operational quantities were first defined in JCRU (lCRP, 1977) and JCRU Report 39 (lCRU, 1985).
Report 39 (ICRU, 1985), and subsequent changes to (13) A brief synopsis of the four following Sections
the definitions were made and described in JCRU that make up this report is as follows:
Report 47 (ICRU, 1992a). The operational quantities • Section 2 defines the quantities used in radiologi-
were developed by the ICRU in response to the needs cal protection, followed by a discussion of the
set out in JCRP Publication 26 (lCRP, 1977) to interrelationships between these quantities. Em-
measure the effective dose equivalent, HE' An impor-
phasis is placed on a description of the theoreti-
tant facet ofthe Task Group's work was to determine
cal basis of both the protection quantities and
whether these operational quantities are still suit-
operational quantities.
able for monitoring the effective dose, E (see Section
5 for discussion). • Section 3 provides a brief summary of the meth-
(9) The operational dose-equivalent quantities de- ods used to calculate the quantities needed.
fined by the ICRU for physical measurement are: • Section 4 gives the conversion coefficients that
• the ambient dose equivalent, H*(d); relate either air kerma free-in-air or particle

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• the directional dose equivalent, H'(d, D); and fluence to the protection and operational quanti-
• the personal dose equivalent, Hp(d). ties. Conversion coefficients are given for organ
(10) These operational quantities, including other absorbed dose, effective dose, ambient dose
related quantities used in radiation protection dosim- equivalent, directional dose equivalent, and per-
etry, are described in JCRU Report 51 (ICRU, 1993b) sonal dose equivalent as appropriate. These data
(see also Section 2 and the Glossary to this report). are given for monoenergetic photons, neutrons,
(11) The purpose of this report is to present and electrons over a limited range of energy and
conversion coefficients for both sets of quantities for several irradiation geometries.
(protection and operational) and to examine their • Section 5 analyses the relationships between the
relationships. Conversion coefficients have been pro- protection and operational quantities, and dis-
duced for idealised irradiation geometries, monoen- cusses the implications of the recommended
ergetic radiations in various anthropomorphic mod- conversion coefficients for radiological protec-
els (mathematical models), and measurement tion. There are two aspects to this analysis:
phantoms. The data given here are intended to
firstly, the influence ofthe various changes in the
provide the basis for comparison between the protec-
new recommendations of the ICRP on both sets
tion and operational quantities and to examine the
of quantities is discussed; secondly, the perfor-
impact ofthe new recommendations on these quanti-
ties. The review of data by the Joint Task Group mance of the operational quantities in monitor-
provides an authoritative and stable data set for ing exposure to external radiation in terms of the
application to dosimetry in radiological protection. protection quantities, as defined in JCRP Publi-
In addition, the data presented also provide a basis cation 60, is reviewed. This review is particu-
for the establishment of calibration programmes. larly important because the set of operational
However, it is not intended to discuss this latter topic quantities, as presently defined, was designed to
in any detail here and the interested reader is monitor the protection quantities recommended
referred to appropriate reports of the International in JCRP Publication 26 and it is necessary to
Organization for Standardization (ISO). understand the performance of these opera-
(12) The data in this report revise and supersede tional quantities in the new regime of JCRP
much of the material in JCRP Publication 51 (lCRP, Publication 60.

2
2. Quantities Used In Radiological Protection For External Radiation

2.1. Introduction the numerical relationship between the physical


(14) Two types of quantities are specifically defined quantities and the protection and operational quan-
for use in radiological protection: protection quanti- tities. These relationships are given in Section 4 and
ties, which are defined by the ICRP, and operational its Annexes in the form of tables and figures in which
quantities, which are defined by the ICRU. The most the conversion coefficients, ElcP, HlcP, E I K a , and
recent set of protection quantities recommended in HI K a , linking the protection and operational quanti-
JCRP Publication 60 (ICRP, 1991a) includes the ties to the physical quantities are presented.
effective dose, E, and the tissue or organ equivalent
doses, H T . These quantities are not directly measur- 2.2. The Evolution of Quantities for
able but are amenable to calculation if the conditions Radiological Protection against
of irradiation are known. External Radiation
(15) The ICRU has defined a set of operational
quantities for area and individual monitoring. These 2.2.1. General

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quantities were developed in response to the ICRP's
recommendations in JCRP Publication 26 (ICRP, (20) Some of the earliest radiological protection
1977) and designed to provide an estimate of the quantities were directly expressed in terms of field
protection quantities in existence at that time (ICRU, quantities. Since the 1950s, following the introduc-
1985, 1993b) and to serve as calibration quantities tion of the concept of the critical organ,8 there has
for dosemeters used in monitoring. For area monitor- been a need to relate parameters of the radiation
ing, the appropriate operational quantities are the field to the absorbed dose (and other dose-related
ambient dose equivalent, H*(d), and the directional quantities) inside the human body to conditions of
dose equivalent, H'(d,n). For individual monitoring, radiation exposure. This brief review, which consid-
the personal dose equivalent, H/d), is the appropri- ers the historical relationship between the protec-
ate operational quantity. These operational quanti- tion and operational quantities, is limited to develop-
ties are defined in the glossary. ments during the past 35 years. The historical
(16) The evolution of these protection and opera- relationship between the two sets of quantities is
tional quantities has led to a system of correlated closely intertwined.
quantities, which is illustrated by the scheme in Fig. (21) The protection quantities have developed
1. A brief history of the development of these quanti- from the concept of dose equivalent through the
ties follows in Section 2.2. effective dose equivalent to the currently recom-
(17) Both the protection quantities and opera- mended effective dose. The operational quantities
tional quantities can be related to the basic physical have developed from the maximum dose equivalent
quantities fiuence, cP; air kerma free-in-air,6 Ka; and (MADE) through the dose-equivalent indexes to the
the tissue-absorbed dose, D (ICRU, 1980, 1993b). currently recommended ambient, directional, and
The physical quantities and operational quantities personal dose-equivalent quantities.
are the basis for measuring external radiation. Na-
tional and international standards laboratories main- 2.2.2. Dose equivalent
tain standards and reference radiation fields that
are specified and described in terms of these quanti- (22) The dose equivalent was defined in a manner
ties for calibration of instruments and dosemeters. similar to that of its predecessor (the RBE dose)
(18) Conversion coefficients,7 which relate opera- following the introduction of the quality factor, Q, to
tional and protection quantities to physical quanti- replace the RBE (ICRP/ICRU, 1963). The dose
ties, are calculated using radiation transport codes equivalent, DE, was expressed in the form
and the appropriate mathematical models. These (DE) = D(QF)(DF) . .. 9 (2.1)
transport codes are described in Section 3, and their
specific application is discussed in Section 4. where D was the absorbed dose in the tissue of
(19) This report presents calculated data and gives interest, modified by several 'modifying factors.' This

6 The quantity air kerma free-in-air is often referred to simply 8 In the 1958 recommendations of the ICRP, the blood-forming
as 'air kerma.' This use may be confusing because it is possible to organs, the gonads and the lenses of the eyes were regarded as
have air kerma in materials other than air, e.g., in a water critical tissues in the case of whole body exposure (ICRP, 1958).
phantom. Unless the circumstances are clear, it is usually better 9 The mathematical symbols in this equation are obsolete. They
to give the full specification. are retained because they are used in the reference cited. In
7 Because conversion coefficients have physical dimensions, this particular, the symbol 'QF' is used for quality factor. Throughout
term is preferred in this report to the term 'conversion factors,' most of this report the currently used symbols 'Q' and 'Q(L), are
which has been used in earlier scientific literature. used for quality factor. 3
Physical quantities

• Fluenc:e, t/)

CalC;U]atcd using ~L) and • Kerma,K

aD/
simple phantoms sphere or Calc;u]atcd using w..' WT,
slab) validated by • Absorbed dose, D and anthropomorphic
measurements
calc;u]ations ~.
Operational quantities Protection quantities
• Ambient dose equivalent, H*(d)
· Organ absorbed dose, DT

L
• Directional dose equivalent, H' (d,il)
· Organ equivalent dose HT
Personal dose equivalent, H,(d) .. ___ Compared by measurement
and calc;u]atlons (us.ing w.., W T ,
and anthropomorphic
· Effective dose, E

phantoms)
Related by calibration
and calculation

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Monitored quantities:
Instrument responses!

Fig. 1. Relationship of quantities for radiological protection monitoring purposes.

was an open-ended definition because only two of the also extended in JCRP Publication 15 (lCRP, 1970)
modifying factors were specified: the 'quality factor' and its supplement, JCRP Publication 21 (ICRP,
(QF) and the 'dose distribution factor' (DF) (ICRP, 1973). JCRP Publication 15 explicitly states: "An
1964). The dose distribution factor and the other alternative approach to the determination of the
modifying factors mentioned in the definition were dose equivalent by the use of quality factors and an
later abandoned. assessment of absorbed dose is to convert the par-
ticle fluence incident upon the body directly by the
use of conversion factors." In addition to giving
2.2.3. The maximum dose equivalent (MADE)
values ofthe 'mean quality factor,'ll Q, for electrons,
(23) The operational quantity corresponding to the neutrons, photons, and protons over a wide range of
dose equivalent became informally known as MADE energy, JCRP Publication 21 also recommended con-
and was later adopted by the ICRU (lCRU, 1971; version coefficients that were intended to facilitate
Patterson and Thomas, 1973). Protection was af- estimation of MADE.
forded by determining the distribution of the point
quantity,lO DE, with depth in a phantom and compar-
ing the maximum of the distribution (MADE) with 2.2.5. Dose equivalent indexes
the prescribed critical organ doses. For low-energy
radiations for which the absorbed dose distribution (25) Many different phantoms were used to calcu-
is steeply declining within the body, only those late MADE, including semi-infinite slabs of tissue-
organs near the surface of the body are irradiated. like material such as water, polystyrene, and the
This technique is conservative. so-called 'standard tissue' [the precursor of ICRU
tissue, see JCRU Report 33 (lCRU, 1980)). Some
calculations were made in finite phantoms (e.g.,
2.2.4. Conversion coefficients parallelepipeds, right cylinders, and elliptical cylin-
(24) Conversion coefficients relating the neutron ders). To standardise the calculation of conversion
fluence rate to the maximum dose-equivalent rate coefficients, the ICRU specified the ICRU sphere as
were given for neutrons up to 30 MeV in NCRP the phantom of choice and MADE in the sphere
Report No. 20 (NCRP, 1957). The ICRP first recom- became more rigorously defined as the dose-equiva-
mended fluence-to-dose-equivalent conversion coeffi-
cients for neutrons in JCRP Publication 4 (lCRP,
1964), which extended recommendations up to neu- II For consistency throughout this report, the term 'mean

tron energies of 1 GeV The recommendations were quality factor,' Q, is used. Other terms used in the literature are
'average quality factor' and, sometimes, 'effective quality factor.'
The reader should be sure of the context in which these terms are
10 In practice this quantity is averaged over a small volume of used: they are often interchangeable but 'effective quality factor'
4 tissue (typically 1 cm 3 ). is used in various ways in the literature.
lent indexes (lCRU, 1976) (see the Glossary to this Publication 21, which was eventually published as
report). ICRP Publication 51 (lCRP, 1987). This revised
report was intended to adapt the data in ICRP
2.2.6. Effective dose equivalent Publication 21 and its underlying approach to con-
form with the basic radiological protection recommen-
(26) In ICRP Publication 26, the ICRP revised its dations issued in ICRP Publication 26 (lCRP, 1977)
basic recommendations and introduced the precur- and its later modifications (lCRP, 1978, 1980, 1985),
sor of the concept of the effective dose equivalent, as and to take account of developments in the ICRV's
a protection quantity to be used in internal dosim- recommendations with respect to the operational
etry (lCRP, 1977). In the Stockholm Statement ofthe quantities (lCRU, 1980, 1985).
ICRP (lCRP, 1978), the effective dose equivalent, HE,
was defined by the equation:
2.2.9. The Paris Statement of the ICRP
(2.2) (ICRP, 1985)
(31) In response to new information on the RBE for
where T represents a tissue or organ of the human neutrons, the ICRP issued a Statement in which the
body, HT is the dose equivalent in tissue (T), and WT

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Commission recommended in the case of neutrons-
is a weighting factor specified by the Commission "an increase in Q by a factor of 2. The permitted
(lCRP, 1977).
approximation for Q for neutrons thus changes from
(27) The intent ofthe effective dose equivalent was
10 to 20. These changes relate only to neutrons, and
to express non-uniform exposures in terms of their
no other changes in Q are recommended at this
equivalent whole-body exposure. Originally con-
time." In the tabulations of conversion coefficients
ceived for internal dosimetry, the concept of the
given in ICRP Publication 51 (lCRP, 1987), this
effective dose equivalent was later also applied to latter recommendation was interpreted by suggest-
external radiation exposure.
ing that the numerical values of conversion coeffi-
(28) The dose equivalent indexes initially re-
cients be increased by a factor of2.
mained the operational quantities of choice recom-
mended for external radiation exposures in ICRP
Publication 26. 2.2.10. ICRU Report 40 (ICRU, 1986)
(32) In 1986 the ICRU published, as ICRU Report
2.2.7. Operational quantities 40, the recommendations of a Joint Task Group of
(29) In 1979, after application of the concept of the the ICRP and the ICRU entitled 'The Quality Factor
effective dose equivalent was extended to external in Radiation Protection' (lCRU, 1986). This report
radiation exposures, the ICRU established a commit- discusses in some detail the role of the quality factor
tee to study methods of determining dose equiva- in radiological protection and its relationship to
lents from exposure to sources of ionising radiation RBE, lineal energy, and linear energy transfer.
outside the human body. On the basis of a review of (33) One of the important recommendations ofthe
the desirable properties of operational quantities, report was that a change in the numerical values of
the committee recommended that the index quanti- the recommended values of the quality factor for
ties be replaced for radiological protection monitor- intermediate and high-LET radiations was indicated
ing by two quantities: the ambient dose equivalent, because the then currently recommended values ofQ
H*, and the directional dose equivalent, H'. The did not provide the same degree of protection for all
committee also recommended adoption of two quan- types of radiation. The Task Group preferred to
tities for individual monitoring: the individual dose specify radiation quality in terms of lineal energy in
equivalent-penetrating, H p , and the individual dose a sphere of ICRU tissue (1 /Lm in diameter) and
equivalent-superficial, Hs. (These quantities are de- provided a relationship between lineal energy and
fined in the Glossary to this report.) The ICRU LET. In addition, a numerical relationship between
accepted these recommendations and they are pub- the quality factor, Q, and lineal energy was proposed.
lished in ICRU Reports 39 and 43 (lCRU, 1985, (34) The recommendations contained in ICRU
1988). A complete and current compilation of all Report 40 were considered by the ICRP when it
operational quantities currently recommended by formulated its new basic recommendations, which
the ICRU is available in ICRU Report 51 (ICRU, were published as ICRP Publication 60 (lCRP, 1991a).
1993b).
2.2.11. ICRP Publication 60
2.2.8. ICRP Publication 51
(35) ICRP Publication 60 introduced several
(30) In parallel with these developments, the ICRP changes of consequence for external radiation dosim-
began preparation of a revised version of ICRP etry. These changes are discussed in detail in this 5
section and in Sections 3-5 of ICRP Publication 60. defined at a point in the tissues or organs of a human
With the publication ofthese revised basic recommen- body or in phantoms (mathematical models) used to
dations, a situation similar to that which occurred in define the operational quantities (lCRU, 1993b).
1977 arises and, just as it was necessary to revise When averaged over tissues and organs, the ab-
ICRP Publication 21, it is now necessary to revise sorbed dose is used to define the protection quanti-
ICRP Publication 51 to adapt its data and underly- ties (ICRP, 1991a).
ing approach to be in accordance with the basic
radiological protection recommendations now pub-
2.3.2. Absorbed dose distributions
lished in ICRP Publication 60. This review is doubly
important because the current ICRU operational (39) For all types of external radiation, determina-
quantities were specified to monitor the protection tion of both the protection and operational quantities
quantities given in ICRP Publication 26 (and its begins with calculation ofthe absorbed dose distribu-
subsequent modifications), which in turn are re- tion in the computational model of the body or
flected in the data of ICRP Publication 51. reference computational model. 12 As described in
some detail in Section 3, such calculations of the
absorbed dose distributions are typically performed
2.2.12. ICRU Reports 47 and 51

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using Monte Carlo codes.
(36) ICRU Report 51 simplified the quantity for
individual monitoring by replacing the individual 2.3.3. Mean absorbed dose
dose-equivalent quantities introduced in ICRU Re-
ports 39 and 43 with the personal dose equivalent (40) The mean absorbed dose averaged over a
(lCRU, 1993b) (see the Glossary to this report). specified tissue or organ, D T , is used to define the
ICRU Report 47 suggested that, for the purposes of protection quantities (ICRP, 1991a). When the ab-
dosemeter calibration for electrons and photons un- sorbed dose distribution in the body or phantom is
der reference conditions (e.g., monodirectional radia- known, calculation of DT is straightforward and
tion beam with frontal incidence), the dose equiva- given by
lent in a 30 cm X 30 cm X 15 cm slab of ICRU
tissue-equivalent material provides an adequate ap-
proximation to the backscatter of the human body so
DT = I/mT i mT
Ddm = I/mT i mT
dE
-d dm
m
(2.3)

that personal dose equivalent in the human trunk at where mT is the mass of the tissue or organ and
a depth of 10 mm may be estimated (lCRU, 1992a). D = dE/dm is the absorbed dose in the mass element,
dm (ICRU, 1993b).
(41) For a detailed description of the calculation of
2.2.13. Summary
the mean absorbed dose in any region, including a
(37) During the 14-year span between ICRP Publi- discussion of the validity of some of the approxima-
cations 26 and 60, the ICRU has continued to tions used [e.g., continuous slowing down approxima-
develop the dosimetric quantities that were first tion (CSDA) and the kerma approximation], see
introduced in 1985. The underlying conceptual frame- Section 3.4.2 'General features of the transport
work of radiation dosimetry embedded in the recom- codes.'
mendations of ICRP Publication 60 represents a
considerable departure from those given in ICRP
2.4. Radiation Weighting
Publication 26. Furthermore, the significant improve-
ments in the mathematical models, transport codes,
2.4.1. General
and physical databases used to determine the neces-
sary absorbed dose (and dose-related) distributions (42) In calculation of both the protection and
warrant a review of the data in ICRP Publication 51. operational quantities, the absorbed dose distribu-
tions are weighted to account for the biological
effectiveness of either the charged particles deposit-
2.3. Absorbed Dose ing the absorbed dose at the point of interaction in
tissue or (since ICRP Publication 60) of the radia-
2.3.1. Absorbed dose tions incident on the body.
(38) The absorbed dose is the quotient ofthe mean (43) The methods of radiation weighting recom-
energy imparted by ionising radiation to matter in a mended in ICRP Publication 60 represent a signifi-
specified volume element divided by the mass of
matter in the volume (see the Glossary in this
12 Throughout this report, the term 'model' has been used in
report). The quantity is defined with the intention of place of the more familiar term 'phantom' except where 'phantom'
providing a physical measure that is correlated with has become an integral part of an expression, as in 'MIRD
6 the effects of ionising radiation. For example, it is Phantom' (see ICRU Report 48) (ICRU, 1992b).
cant departure from the recommendations in ICRP component are then added. In the case of neutrons,
Publication 26, in which the same method of radia- the radiation-weighting factor varies with energy
tion weighting was recommended for both the protec- and the computation is made by integration over the
tion and the operational quantities, the weighting entire energy spectrum.
factor, called the quality factor, Q, being determined
by the Q(L) - L relationship and the value of L (the
linear energy transfer in water) at the point of 2.4.3. Radiation weighting factors
interaction. In ICRP Publication 60, ICRP now speci- for electrons and photons
fies a new radiation weighting factor, WR, for the
(46) The radiation-weighting factor, WR, is defined
protection quantities while the method proposed by
to be unity for electrons and photons of all energies
the ICRD for the operational quantities remains
unchanged [although specific changes in the Q(L) - L (Table 1 of ICRP Publication 60). Consequently, the
equivalent doses are numerically equal to the ab-
relationship are made]. The new radiation-weight-
sorbed doses at the point ofinterest.
ing factor, WR, is determined by the radiation inci-
dent on the body and is applied to the mean absorbed
dose over the organ or tissue of interest. The quality
2.4.4. Radiation weighting factors

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factor is still applied to the absorbed dose at the
point of interaction. for neutrons
(47) The ICRP-recommended radiation-weighting
2.4.2. Radiation weighting for protection factors, WR, as a function of neutron energy (Table 1
quantities of ICRP Publication 60) are reproduced in the Glos-
sary to this report. As an approximation to the
(44) For the protection quantities, the ICRP has values of WR, the ICRP also recommended the rela-
defined the radiation-weighting factor, WR, by which tionship given in Annex A of ICRP Publication 60 for
the organ absorbed dose is multiplied to account for convenience in calculation of radiation weighting
the relative detriment of different types of radiation. factors for neutrons, wR(E n ):
Numerical values ofwR specified in terms of type and
energy for most, but not all, radiations incident on
the body are given in Table 1 in ICRP Publication 60 (2.5)
(and reproduced in the Glossary of this report).
Furthermore, "for radiation types and energy that where En is the neutron energy in MeV. The values of
are not included in this table, an approximation of WR given by this equation have been used to evaluate
WR can be obtained by calculation of Q at a 10 mm the reference data for neutrons.
depth in the ICRD sphere:

-
Q = 151 JrL Q(L)D(L)dL (2.4) 2.4.5. Radiation weighting for operational
quantities
where D(L)dL is the absorbed dose at 10 mm be- (48) The operational quantities are defined at a
tween linear energy transfer Land L + dL; and Q(L) point in tissue or a phantom in terms of the quality
is the quality factor of L at 10 mm" (Paragraph A14, factor, Q, and the absorbed dose, D. The quality
ICRP Publication 60). The symbol D(L)dL has histori- factor, which is to be applied to the absorbed dose
cally been used by the ICRP for the absorbed dose deposited by a charged particle, is obtained by
between linear energy transfer, L, and L + dL. ICRD assuming that the stopping power of the particle in
uses DLdL for the same quantity. In both instances, water is numerically equal to L in the appropriate
the more usual mathematical symbol would be Q(L) - L relationship.
dD / dL whence:

Q = - Ii Q(L) . -dD . dL (2.4a) 2.4.6. Q(L) - L relationship


DL dL
(49) The quality factor has a functional depen-
An important distinction between Q and WR is that, dence on the linear energy transfer, L, in water. The
whereas the former is a direct function of L, the numerical relation between Q(L) and L specified by
latter is related to relative biological effectiveness the ICRP in Table A-I in Annex A of Publication 60
and is only indirectly related to L. and shown in Fig. 2 is given by three equations:
(45) If the body or a phantom is irradiated by
different types of radiation, each with its own radia- Q(L) = 1 (L < 10 keVlJlm) (2.6a)
tion-weightingfactor, the absorbed doses and equiva- Q(L) = 0.32L - 2.2 (10:::; L :::; 100 keVlJlm) (2.6b)
lent doses are usually calculated separately for each
radiation. The contributions from each radiation Q(L) = 300/,)L (L> 100 keV/Jlm) (2.6c) 7
(53) Values of Qn(En) have been calculated as a
- - - - Q(L) ICRP Publi:adoa 26 function of neutron energy by Schuhmacher and
25 --- Q(L) ICRP Publi:adon 60
Siebert (1992).
(54) If a value of the mean quality factor over a
~20 volume (such as a tissue or organ) is required,
~15 dose-weighted averaging over the volume must be
applied and Q is given by:

Q
1
= --
i r de(L)
J, Q(L)--dLdm. (2.9)
5 mTDT mT L dm

2.4.8. Stopping power


Fig. 2. Quality factor as a function oflinear energy transfer as (55) The quality factor, Q, is defined as a function
recommended in ICRP Publications 26 and 60.
of the unrestricted linear energy transfer, L, in water
(see Glossary). The Q(L) - L relationship has been

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selected by the ICRP to provide, amongst other
There is a trivial discontinuity atL = 100 keV//Lm, things, values ofQ for neutrons compatible with the
which needs to be recognised when computer calcula- available information about the relative biological
tions are made. effectiveness of neutrons for biological endpoints
(50) Section 2.4.2 discusses the combined inft.uence relevant to the induction of stochastic effects in man.
on conversion coefficients of changes in the ICRP- In particular, the choice of the 1990 relationship was
recommended Q(L) - L relationship and in charged- intended to provide a value of Q of about 20 for
particle stopping powers. This relationship was used neutrons with energies around 1 MeV. The linear
to calculate the conversion coefficients recommended energy transfer is numerically equal to the stopping
in ICRP Publication 51 (lCRP, 1987), and in this power, S, of charged particles in water. Since the
report, for comparison of data for HE and E. The Q - issue of ICRP Publication 51, new values of the
L relationship recommended in Publication 60 was stopping power have been recommended for protons
used in new calculations of the operational quanti- and alpha particles (lCRU, 1993a). Data are now
ties, H*, H', and H p , given in this report (see Section available for water in both the liquid and vapour
5). phases, whereas earlier data were for water only in
the vapour phase. Any significant change in the
values of L would call for a revision of the Q(L) - L
2.4.7. Mean quality factor, Q
rela tionshi p.
(51) The quality factor averaged over an absorbed (56) The new values of stopping power in liquid
dose spectrum in L may be obtained by integrating water have been used with the 1990 Q(L) - L
over the entire spectrum in L: relationship by the authors whose data have been
summarised in this report, so it was important to
Q = r
JL
Q(L)' dD. dL/ r dD. dL
dL JL dL
(2.7) consider the magnitude of the effect on Q of the new
values of L. The effect, shown by two of the curves in
(52) For external irradiation by neutrons, the Fig. 3, is a reduction in Q by no more than about 20%
value of Q at a point of interest in a tissue phantom and is not sufficient to make the values of Q incom-
may be determined by separately considering the patible with the RBE data. It is therefore not neces-
neutron and secondary photon contributions to the sary to change the 1990 Q(L) - L relationship.
absorbed dose, then calculating an absorbed dose Figure 3 also shows the 1978 values ofQ for compari-
weighted mean of the corresponding quality factors. son. The values of WR are not affected by changes in
The acceptable approximation for the value of Q for stopping power.
secondary photons is taken to be unity. The value of (57) For comparison, the radiation-weighting fac-
the mean neutron quality factors, Qn, is calculated tor, WR (lCRP, 1991a), is indicated by a solid line and
from: the approximation to WR is shown by a dashed line.
For a detailed discussion of the inft.uence of the
changes on the stopping power, see Siebert and
Schuhmacher (1995).
where En is the neutron energy, kr (En) is the tissue (58) In summary, changes in the stopping power
kerma coefficient for neutrons at energy E, rp(En) is only directly affect the operational quantities. By
the neutron ft.uence at the point of interest, and virtue of the definition of the protection quantities,
Qn(En) is the neutron quality factor for a small their numerical values are not directly affected.
8 volume of tissue irradiated by neutrons. Nevertheless, the values of WR recommended by the
20 v H+(lO)/D+(lO), Q(L) and L new
H+(lO)ID+(lO), Q(L) new, L old
If+(lO)ID·(lO), Q(L) and L old
Fig. 3. A summary of the influence of the Q(L) - L IS
w.
relationship and charged-particle stopping power on the
mean quality factor, Q, for the ambient dose equivalent (see
text for further discussion). [The symbols H*(10) and 10
/ ..;
D*(10) are the ambient dose equivalent and ambient
absorbed dose at 10 mm, respectively.J
...
I
.
v'

:';.
5 ..
• v
; vv •• ;
...... ...... . .. . ........
; ; ; HUH,,;,''r
./

o~~~~~~~~~~~~~~--~~~~~~
1~ 1~ 1~ 1~ 1~ 1~ l~ l~ 1~ 1~ l~ 1~
Neutron energy (MeV)

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ICRP for neutrons do indirectly depend upon many consisting of several radiations with different values
parameters, including the unrestricted linear energy of WR, the absorbed dose must be subdivided in
transfer. Figure 3 shows that values ofQ estimated blocks, multiplied by its own value ofwR and summed
from eqn (2.4) and the currently recommended Q(L) - over the different radiations, R, i.e.,
L relationship are in fair agreement (see also Para-
graph A14 in Annex A of ICRP Publication 60). It is (2.11)
desirable to continuously evaluate recommended
values of radiation weighting factors and quality where DT,R is the average absorbed dose from radia-
factors in their relation to both physical and radiobio- tion, R, in tissue T.
logical data so as to provide adequate protection and
better consistency between the protection and opera-
tional quantities. For a discussion see Dietze and 2.5.4. Effective dose
Siebert (1994), Siebert (1994a,b) and Siebert et al.
(1995). (62) The effective dose, E, is the sum of the
weighted equivalent doses in all the tissues and
organs ofthe body. It is given by the expression:
2.5. Radiological Protection Quantities
(2.12)
2.5.1. General
(59) Protection quantities were recommended and where HT is the equivalent dose in tissue or organ T
defined by the ICRP in Publication 60 for radiologi- and WT is the weighting factor for tissue T.
cal protection purposes. These quantities include the (63) For the purpose of radiological protection
organ absorbed dose, the equivalent dose in an organ calculations, the human body is defined in ICRP
or tissue and the effective dose. Publication 60 by 12 designated tissues and organs,
and the remainder, which consists of 10 additional
tissues or organs. Recommended weighting factors,
2.5.2. Organ absorbed dose which apply to a human adult population for these
(60) The mean absorbed dose, D T , in a specified tissues or organs, are given in ICRP Publication 60
tissue or organ of the human body, T, is given by and are also in the Glossary to this report.
(64) The data presented in this report were calcu-
(2.10) lated with a remainder, defined as it was in ICRP
Publication 60, consisting of 10 tissues and organs.
where mT is the mass ofthe tissue or organ, and D is The ICRP revised its specification of the remainder
the absorbed dose in the mass element dm. A more to include only nine organs (lCRP, 1995a). The upper
precise definition is given in Paragraph (40). large intestine was removed from the list of remain-
der tissues and organs because it is already included
amongst the designated tissues and organs as the
2.5.3. Equivalent dose
colon. In ICRP Publication 71 (ICRP, 1995b) the
(61) To determine the total equivalent dose, H T , in Commission added the extrathoracic airways to the
a tissue or organ, T, irradiated in a radiation field remainder. The value of the remainder equivalent 9
dose is not much affected by this change and the external exposure and for the irradiation geometries
impact on the effective dose is negligible. discussed in this report, a simplified procedure may
be adopted in which footnote 3 is not invoked and the
arithmetic average (not mass-average) of the indi-
Conventions for calculating effective dose vidual remainder organ dose contributions is com-
(65) There are significant differences in the pub- puted (Hollnagel et al., 1994; Zankl and Drexler,
lished scientific literature in the way in which the 1995). This simplified procedure was adopted for the
value ofthe effective dose is calculated. For a consis- data reported here; the influence on the value of the
tent approach in the analysis of various data sets to effective dose is very small (a few percent).
determine the effective dose conversion coefficients
(see Section 4.1) from published tissue and organ
2.6. Operational Quantities
equivalent dose data, conventions with respect to
summation of tissue and organ doses and the evalua-
2.6.1. General
tion of the remainder dose were used in this report.
(70) The operational quantities defined by the
ICRU (ICRU, 1985, 1988, 1992a, 1993b) are related

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Tissue and organ dose summation to the ICRP protection quantities, and are intended
procedure to provide a reasonable estimate of the protection
(66) The effective dose was calculated using tissue quantities in assessing compliance with the limits.
and organ dose equivalent data available for female These operational quantities were designed to meet
and male mathematical models and application of the needs of the recommendations in ICRP Publica-
the following formula: tion 26.
(71) One important function of the Task Group was
E = WbreastHbreast,female + to determine the degree to which the operational
~ WT [HT,male + HT,female] quantities still provide reasonable estimates of the
~ (2.13) newly specified protection quantities. Section 5 dis-
T*bread 2 cusses the conclusions ofthis study. For area monitor-
where the symbols have their usual significance. ing, the operational quantities are the ambient dose
Equation (2.13) was originally derived for calcula- equivalent, H*(d), and the directional dose equiva-
tion of the effective dose equivalent, HE (Kramer and lent, H'(d,D). For individual monitoring, the per-
Drexler, 1982) and modified to include the new sonal dose equivalent, Hp(d), defined in the body, is
tissues and revised tissue-weighting factors recom- the operational quantity.
mended in ICRP Publication 60 for calculation of the
effective dose, E,
(67) In those cases where published data did not 2.6.2. Dose equivalent
give separate organ dose data for female and male (72) The dose equivalent, H, at a point is given by
models, eqn (2.12) was used directly in evaluation of
the data given in this report.
(68) The definitions of equivalent dose (in a single
H = J, Q(L) . dD
L dL
. dL (2.14)
tissue or organ) and effective dose (in the whole where Q(L) is the quality factor for particles with
body) are not confined to any particular set of values linear energy transfer, L, and dD/dL . dL is the
of the weighting factors WR and WT, so care is needed absorbed dose between linear energy transfer, L, and
to avoid ambiguity. When the ICRP uses equivalent L + dL at the point.
dose and effective dose, it will be implicit that these
contain the values of radiation and tissue weighting
factors recommended at the relevant time. If values 2.6.3. Operational quantities for area
of weighting factors other than those recommended monitoring
by the ICRP are used, this fact should be clearly
stated and the values should be explicitly given
when the quantities are introduced. Expanded and aligned fields
(73) For the operational quantities-ambient dose
equivalent, H*(d), and directional dose equivalent,
Remainder dose evaluation
H'(d, D)-the ICRU has introduced the concepts of
(69) The complete specification of the remainder alignment and expansion of the radiation field. An
dose incorporates footnote 3 of Table 2 (ICRP Publi- expanded radiation field is defined as a hypothetical
cation 60) and mass weighting ofthe contributions of field where the fluence and its angular and energy
the individual organs that make up the remainder distributions have the same value throughout the
10 (ICRP, 1991b). Analyses show that in the case of volume of interest as that in the actual field at the
point of reference. An expanded and aligned radia- Specified direction
tion field is a hypothetical field where the fluence
and its energy distribution are the same as an
expanded field, but the fluence is unidirectional.
0/ Unidirectional
field

Point of _--:-..,..:.+.•
measurement

Ambient dose equivalent


H'(d.cr)
(74) The ambient dose equivalent, H*(d), at a point
in a radiation field is the dose equivalent that would
be produced by the corresponding expanded and
aligned field in the ICRU sphere at a depth, d, on the
radius opposing the direction of the aligned field.
The recommended value of dis 10 mm for penetrat- Specified direction
ing radiation and 0.07 mm for low-penetrating radia- normal to surface
tion.
0/ Unidirectional
field

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Directional dose equivalent
(75) The directional dose equivalent, H'(d,D), at a
point in a radiation field is the dose equivalent that
would be produced by the corresponding expanded
field in the ICRU sphere at a depth, d, on a radius in
a specified direction, n. The recommended value of d
for penetrating radiation is 10 mm and for low- Phantom or body
penentrating radiation it is 0.07 mm. Fig. 4. Definition of the angle Ci for H'(d, Ci) and Hp(d, Ci).
(76) Any statement on the directional dose equiva-
lent should include specification of the reference
depth, d, and the direction, n. To simplify notation, d
should be expressed in millimetres. This reference both between individuals and between locations on
system can often be related to the radiation field. In any given individual. The personal dose equivalent
the particular case of a unidirectional field, the is thus a multi-valued quantity (Wagner, 1987).
direction can be specified in terms of the angle, a, (80) So that single-valued conversion coefficients
between the radius opposing the incident field and may be calculated, it is first necessary to specify a
the specified radius (see Fig. 4). When a = 0°, the particular location on the human body. Second, in
quantity H'(d, 0°) may be written as H'(d) and is order to facilitate such calculations and dosemeter
equal to H*(d). calibrations, it is desirable that anthropomorphic
(77) The angle a may be related to the irradiation phantoms of various parts ofthe body be specified. In
geometries described in Section 3.5. For the AP general, with one exception, such phantoms have not
geometry a = 0°; for the LAT geometry a = 90°, and yet been specified by the ICRU.
for the PAgeometry a = 180°. (81) The one exception to this general rule is for
the human trunk. The ability to interpret the read-
ings of dose meters worn on the human trunk in
2.6.4. Operational quantities for individual terms of the protection quantities is of the greatest
monitoring
interest for monitoring external radiation exposure.
For the purposes of dosemeter calibration, phantoms
have been specified that are often taken to be
Personal dose equivalent
surrogates for the human torso. These simplified
(78) Instead ofthe two quantities (individual dose tissue-substitute phantoms are the ICRU tissue-
equivalent, penetrating; and individual dose equiva- equivalent sphere (30 cm diameter) and the 30 cm X
lent, superficial) defined in ICRU Report 39 (ICRU, 30 cm X 15 cm ICRU slab (lCRU Reports 47, 48 and
1985), a simplified concept called the personal dose 51, ICRU, 1992a,b; 1993b). Section 4 reviews and
equivalent, Hp(d), was recommended in ICRU Re- summarises the data that are currently available for
ports 47 and 51 (ICRU, 1992a, 1993b). Hp,slab and Hp,sphere'
(79) Personal dose equivalent is defined in the (82) Until calculations in the human trunk for
human body and, because of scattering and interac- various irradiation geometries and radiation ener-
tion of radiation in the body (which depend on the gies are available, it is not possible to estimate
material composition and geometry), Hp(d) can vary precisely how calculations of the conversion coeffi- 11
cient in the slab or sphere phantoms replicate the example, the thymus and testes are of a suitable size
personal dose equivalent in the body but the errors and at a suitable depth for the purposes of inferring
involved are thought to be small. the results of more precise calculations. This matter
(83) In the interim, general conclusions about the is discussed in more detail in Section 5.
relationship between Hp(d), and E may be inferred (84) The practical realisation of the personal dose
from available phantom and organ dose data. Com- equivalent requires agreement on an expedient met-
parisons may be made with average doses to small rological procedure (Wagner, 1987). See Sections 4
organs located near the surface of the body. For and 5 for a discussion of this procedure.

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12
3. Determination of Absorbed Dose Distributions In The Human Body
and In Anthropomorphic and Other Models

3.1. Introduction characteristics of the human body that are them-


selves subject to considerable variations between
(85) The two sets of quantities used in radiological
individuals depending on sex, age, body weight, and
protection for exposure by sources of radiation out-
side the body are protection quantities and opera- height. Thus, determination ofthe absorbed dose is a
tional quantities (see Section 2 for discussion). The complex problem that can be approximately resolved
operational quantities used in measurement were by experimental and calculational approaches. In
designed to provide a reasonable estimate of the practice, large uncertainties in estimation of the
appropriate protection quantity under normal work- absorbed dose distributions may arise due to a lack
ing conditions. For external irradiation of the body, of detailed knowledge of the radiation field.
this may be simply expressed by the goal that the (90) The experimental approach requires construc-
ratio of the value of the appropriate protection tion of a realistic phantom of the human body using
quantity (Hprot ) to the measurement of the opera- tissue-equivalent material and an extensive measure-

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tional quantity (Hop) is usually less than unity. ment programme. Accurate measurements require
Under this condition, the operational quantity pro- considerable effort and resources, particularly for
vides an overestimate of the protection quantity, radiations with a quality factor or a radiation-
(3.1) weighting factor greater than 1. The resources re-
quired for such an experimental programme are
Thus, it is necessary to relate these two types of generally beyond all but the largest laboratories.
quantity. Under known conditions of irradiation, the Consequently, the number of systematic experimen-
values of both quantities may, in principle, be calcu- tal determinations of the absorbed dose described in
lated.
the scientific literature is limited.
(86) This section and the following sections sum-
(91) Considerable effort is required for calculations
marise how the basic calculations (absorbed dose
of the absorbed dose distribution in mathematical
distributions 13 ) necessary for this comparison may
be carried out. Calculations for the operational quan- computational models. However, modern computing
tities may be confirmed by measurement. methods (particularly Monte Carlo techniques) have
(87) To compare the values of the protection quan- the advantage in that they can deal with complex
tities and operational quantities caused by external irradiation conditions and provide absorbed dose
exposure of the human body to ionising radiation, it distributions in a wide variety of radiation fields. In
is necessary to know the distribution ofthe absorbed addition to statistical uncertainties inherent in such
dose throughout the actual human body or computa- calculations, other uncertainties may arise from
tional model. From this known distribution of the several sources (e.g., the data used to simulate
absorbed dose, the quantities, which are related to radiation interactions with tissue; differences in
absorbed dose, may be calculated. anatomical modelling; and the inherent variation in
(88) Calculation of the absorbed dose distributions human anatomy).
requires knowledge and understanding of the radia- (92) For the purpose of radiological protection,
tion environment; great precision or accuracy is not required in these
• a detailed phantom (model) ofthe human body; calculations. However, to detect possible bias, it is
• knowledge of the geometrical conditions under most important to compare the results obtained by
which the body is irradiated; and several types of calculations, particularly those made
• a method of calculating the radiation interac- in differing computational models and by different
tions in the tissues of the body and transport of
computational techniques. Such comparisons re-
the radiation through the body.
quire appropriate precision in the calculation, even if
(89) The absorbed dose distribution and dose-
this precision is not strictly needed for radiological
related quantities in a human body or computational
model are dependent on the energy spectrum and protection.
angular distribution of the incident radiation and
the orientation of the body in the radiation field. The
absorbed dose distribution is also dependent on the 3.2. Radiation Field
(93) A radiation field can be defined by the direc-
tional and energy distributions of all types of par-
13 Absorbed dose distributions weighted by WR are used as the
basis for calculations of HT and E but dose equivalent distribu- ticles of which it is composed. Reference radiation
tions are obtained by weighting by Q. fields are specified in terms offield quantities, which 13
are normally air kerma free-in-air14 for photons and proximation is valid for energies up to about 3 MeV
fluence for neutrons. The units of these field quanti- (Dimbylow and Francis, 1983, 1984; Drexler et al.,
ties may be realised by primary standards or refer- 1989a; Ferrari and Pelliccioni, 1994b; and Hollnagel
ence instruments at Standards Laboratories. Most of et al., 1984). For neutrons, the approximation is
the data in this report were calculated for monoener- valid for energies up to 5 MeV at a depth of 0.07 mm
getic radiations. The external incident radiation and for energies up to about 20 MeV at depths of 3
field specified is that which would have existed had and 10 mm CHollnagel et al., 1984). It may be
the phantom not been present. concluded that, with the exception of the skin, the
(94) The radiation fields of practical interest in kerma approximation is valid for calculation of or-
radiological protection are complex in character and gan doses up to neutron energies of about 20 MeV.
determinations of organ dose may be complicated The skin contributes only about 1 % of the effective
and uncertain. One common source of uncertainty is dose and use of the kerma approximation to calcu-
non-uniformity of the radiation field in which people late E appears to be justified.
are exposed. Non-uniformity of the dose distribution (97) In the case of photon irradiation, the kerma
over volumes as large as a human being is likely approximation assumes that secondary electrons are
under conditions of occupational exposure and is in equilibrium with primary photons at the point of

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almost certain in medical exposure. Radiation fields interest in the phantom, and that the dose equiva-
consisting of only monoenergetic, unidirectional ra- lent is therefore equal to tissue kerma minus
diations of one type of radiation are rare. Radiation bremsstrahlung radiation losses. This is a good
fields with radiation energies distributed over a wide approximation for photons up to 3 MeV. At higher
energy range are referred to as 'broad energy spec- photon energies, the equilibrium becomes increas-
tra.' Furthermore, the radiation fields of practical ingly incomplete and, although secondary electrons
importance in radiological protection often consist of do originate in air and accompany the incident
more than one type of radiation; these are referred to photon beam-somewhat compensating for this lack
as 'mixed fields.' To apply the data given in this of equilibrium-the assumption of charged-particle
report (for monoenergetic radiations) to mixed radia- equilibrium is no longer valid.
tion fields and/or broad spectra, it is necessary to (98) Early calculations showed that the inclusion
calculate the desired quantities averaged over the of the dose equivalent produced by photons scatter-
radiation spectra. ing in the surrounding air, which subsequently inter-
(95) In all cases, assumptions made about charged act with the sphere, contributes about 2% ofthe dose
particle buildup within the model (or phantom) will equivalent at a depth of 10 mm (Dimbylow and
influence the value of the absorbed dose calculated at Francis, 1983; Hollnagel et al., 1984). Calculations
any depth. The depth in the model at which charged were also carried out in vacuo (Dimbylow and Fran-
particle equilibrium is achieved depends upon the cis, 1984).
energy and type of the incident radiation. Most (99) This topic has been revisited more recently by
calculations are performed assuming that charged Ferrari and Pelliccioni (1994a), who question whether
particle equilibrium exists at the point of interest assumptions about interactions with air are strictly
and by applying the kerma approximation. The compatible with the definition of the ambient dose
kerma approximation assumes that, at the point of equivalent in an aligned field. These authors sug-
interest in the phantom, all secondary radiations gested that calculations should always be performed
and, particularly, charged particles are in equilib- in vacuo because, in practice, incident radiation
rium with the primary radiation and, consequently, (after being scattered in air) can be neither aligned
the absorbed dose is equal to the tissue kerma less nor expanded. The authors further suggested that,
any energy removed by uncharged radiation at photon energies above 3 MeV, the quantity ambi-
(bremsstrahlung or neutrons). With the additional ent dose equivalent as defined in fCRU Report 39
assumption of radiation equilibrium, these losses cannot be used for operational radiation protection
will be zero. With the exception of neutrons above 20 purposes. However, the Commissions take the view
MeV, the kerma approximation was used in all the that the secondary charged products (particularly
radiation transport calculations in anthropomorphic electrons) resulting from interactions in air between
phantoms given in this report. This approximation the radiation source and detector (point of interest)
greatly reduces the complexity of radiation transport must be determined and allowed for in any proper
calculations, but it is important to be aware of its calibration procedure.
limitations. (100) Thus, for photons with energies above about
(96) Several authors have examined the accuracy 3 MeV, it is necessary to take account of the air-
of the kerma approximation. For photons, the ap- scattered radiation that depends strongly on the
geometry of source and recipient. This may be done
14 In further text throughout this section, the quantity air by using build-up layers of appropriately selected
14 kerma free-in-air is usually referred to simply as 'air kerma.' thickness. Calculated conversion coefficients assume
that secondary charged-particle equilibrium exists years to enable its use in calculation of absorbed
at the point in the radiation field where a measure- doses from external radiation.
ment is made. (105) The MIRD phantom is analytically defined
in sections: an elliptical cylinder represents the
arms, torso, and hips; truncated elliptical cones
3.3. Models and Phantoms of the represent the legs; and an elliptical cylinder repre-
Human Body sents the head and neck. The arms are not separated
from the torso. In the earlier version of the model, no
3.3.1. Reference man separation is assumed for the legs, but they are
separated in the 1978 version. No models have been
(101) Guides for the design of human body models
adopted for small organs (e.g., nose, ears, feet, and
and phantoms used in radiological protection may be
fingers), for which few data exist regarding their risk
found in ICRP Publication 23 (ICRP, 1975) and
to radiation-induced cancer. Other organs are repre-
ICRU Report 48 (ICRU, 1992b). These reports pro-
sented by simple geometric approximations that are
vide a comprehensive review of the human anatomi-
consistent with the actual shape of the organs. To
cal, physiological, and metabolic characteristics and
minimise computer effort, the mathematical expres-
recommend 'typical' or 'reference' values.
sions used to simulate an organ's size and shape are

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kept as simple as possible.
(106) The MIRD phantom incorporates different
3.3.2. Simple phantoms
densities for the various body tissues. The three
(102) It is not possible to produce either a math- distinct types of tissues identified are skeletal tis-
ematical model phantom or a physical phantom that sues, the lungs, and soft tissue. The model's skin is
can precisely simulate the human body, but it is represented by a 2 mm layer of soft tissue covering
possible to provide phantoms or models that can the whole body. The skeletal tissue includes the
serve as approximate surrogates. Simpler phantoms active bone marrow (red), and all skeletal compo-
are constructed using tissue substitutes, idealised nents are homogeneously distributed in the skel-
organ volumes, and special cavities in which the eton. For the lungs and soft tissue, the most impor-
dosemeters may be located to make in situ measure- tant components of human tissues are hydrogen,
ments. For example, there are phantoms with den- carbon, nitrogen, and oxygen, with trace amounts of
sity-adjusted lungs and bone structures [for a descrip- other elements. The skeletal tissues contain signifi-
tion, see ICRP Publication 51 (ICRP, 1987)]. Water cant proportions of calcium and phosphorus. The
phantoms are also adopted, particularly in medical lungs are slightly different from soft tissue because
physics, for determination of dose distributions in they contain air and almost no fatty tissue. The
patients. Solid homogeneous phantoms in tissue densities of the skeleton, lungs, and soft tissue are
substitutes are widely used for measurements of approximately 1.5, 0.3, and 1.0 g cm -3, respectively.
absorbed dose distributions for photons and neu-
trons. Age- and sex-specific models
(103) Spherical and slab phantoms are convenient, (107) Over the past 10-15 years, the models used
simple approximations to the human body. A spheri- in calculation of the absorbed dose distributions
cal model that is 30 cm in diameter and composed of have become increasingly realistic. Recent impor-
ICRU (soft) tissue-equivalent material is used in the tant improvements in the MIRD phantom have been
definition of the operational quantities (see Section the introduction of male and female models and the
2). Both spherical and slab phantoms are discussed development of child and infant models for absorbed
in more detail later, see the subsection below entitled dose calculations. The original MIRD phantom was
'Standard and reference models and phantoms for hermaphrodite and included the gonads of both
operational measurements.' sexes, and female breasts.
(108) Sex-specific adult models have been devel-
oped to reflect the genuine differences in organ size
3.3.3. Anthropomorphic models and tissues. Cristy (1980) has designed models for
adults and children represented by body sizes corre-
sponding to the ages of 0, 1, 5, 10, and 15 years. The
MIRD phantom
most recent version of these models was published
(104) The Medical Internal Radiation Dose (MIRD) by Cristy and Eckerman (1987). Adult sex-specific
Committee phantom (the original model) is a hetero- models (ADAM and EVA) have also been developed
geneous mathematical representation of the human by Kramer et al. (1982). These models, whose body
body that was first designed to calculate absorbed and organ dimensions are similar to those used in
doses from internal radiation (Snyder et al., 1969, ICRP Publication 23 (ICRP, 1975), are closely re-
1978). This model has been modified over several lated to the MIRD phantom. 15
(109) By contrast, the most recent developments sen ted in most mathematical human models. Hollna-
(CHILD and BABY) belong to a new generation of gel (1992, 1994a) represented the muscle tissue by
models compiled from computer tomographic (CT) three regions, one situated in the trunk and the
data of real patients (Zankl et al., 1988; Veit et al., others located in the arms and legs, whereas Yamagu-
1989). The CHILD model is based on CT data for a chi (1994b) and Zankl and Drexler (1995) repre-
7-year-old child, and the BABY on data for an sented the muscle tissue as occupying one volume in
8-week-old baby. These models are specified by a the torso that is not associated with any other organ.
large number of volume elements (voxels)-approxi- (114) A detailed analysis of the differences of the
mately 20 and 3 mm 3 in volume, respectively. various models used in the calculations described
(110) It is important to point out the improvement and their influence on the scatter of results is beyond
in more recent paediatric models over the earlier the scope of this report (see Sections 4.3.4 and 4.4.4).
models. Whereas the first paediatric models devel-
oped at Oak Ridge National Laboratory (ORNL) are Standard and reference models and phantoms
merely scaled-down versions ofthe adult, later modi- for operational measurements
fications take advantage of the knowledge ofpaediat-
ric anatomy and human growth. In the newest (115) Radiation transport calculations have been
carried out for a wide variety of radiation types and

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paediatric models, the organs are 'lifelike.' Cristy's
models, which date from 1980, combine the data on energies in homogeneous models of different shapes,
human organ size available at ORNL and are correct including spheres, slabs, cubes, and elliptical cylin-
with respect to organ size. These models were used ders. The ICRU has defined operational quantities in
by Yamaguchi (1992, 1994b,c). In the tomographic a spherical tissue-equivalent model (ICRU, 1985,
models developed by Zankl and co-workers, the 1988), at specified locations. Calculations allowed for
organs are reconstructed from CT data for a baby comparison between these quantities and the protec-
and child and replicate as accurately as possible the tion quantities in anthropomorphic phantoms. Vari-
shapes identified on the CT images. ous tissue substitutes are available for fabrication of
corresponding physical phantoms, including tissue-
equivalent material, water, and perspex.
Conformity with ICRP specifications (116) Since 1985, the ICRU sphere model has been
used to define operational quantities for area moni-
(111) In ICRP Publication 60, the number of toring. For individual monitoring, the operational
organs specified was increased compared to that quantities have been defined in soft tissue in the
specified in ICRP Publication 26. Not all the organs human body and are intended to be measured using
and tissues currently specified by the ICRP were individual dosemeters. But to facilitate the calibra-
initially modelled in ADAM, EVA, and MIRD-5. tion of these dosemeters, the dose equivalent at an
There has been an evolution in the modelling in an appropriate depth, d, either in the ICRU sphere or in
attempt to satisfy the ICRP specifications. Several a 30 cm X 30 cm X 15 cm slab ICRU tissue-
groups have developed models that differ somewhat substitute phantom, has been taken to correspond to
from one another in their precise detail. the quantity Hp(d) in the human torso. The quanti-
(112) One example of such development has been ties calculated in the sphere or slab are designated
the addition of the oesophagus to the models. This by the symbols Hp,sphere or Hp,slab in this report (see
organ has been represented by a hollow circular Section 2.6.4).
cylinder, which extends from the superior surface of (117) For several practical reasons, the use of slab
the trunk vertically downwards to the level of the phantoms with compositions other than ICRU tissue
base of the lungs (thoracic region); together with an substitute has been recommended for the purpose of
inclined solid circular cylinder (abdominal region), calibration. Perspex- and water-slab phantoms have
which extends from the base ofthe thoracic region to been recommended by the ICRU and ISO, respec-
a point 1 cm below the fundus of the stomach (Lewis tively (ICRU, 1992b; ISO, 1992, 1993, 1995a,b),
and Ellis, 1979; Hollnagel, 1992). Yamaguchi (1994b) because backscattering conditions are similar to
also modelled the oesophagus in two parts (an ellipti- those from the tissue-substitute slab. Calibration of
cal tube descending along the spine from the neck to personal dose meters usually has been performed on
the diaphragm and an inclined tube linking the end the front surface ofthese slab phantoms.
of the elliptical tube to the upper part of the stom-
ach), whereas Zankl et al. (1992) modelled it as one
3.4. Methods of Calculating Absorbed Dose
single elliptical cylinder ranging in height from
Distributions
within the neck down to the level of the top of the
stomach.
3.4.1. Introduction
(113) A further example illustrating how these
models may differ is in the description of the distribu- (118) A detailed description of the methods used to
16 tion of muscle tissue, which is not explicitly repre- calculate the absorbed dose distribution and dose-
related quantities in phantoms is beyond the scope of doses calculated with the kerma approximation and
this report. Only a brief review is given here because by modelling the energy deposition by secondary
extensive reviews exist in the scientific literature electrons with a simplified CSDA. For neutrons, the
[see, for example, ICRP Publication 51 (lCRP, 1987) validity of the kerma approximation is restricted by
and NCRP Report No. 108 (NCRP, 1991)]. Sections the range of recoil protons, which in water is about
4.3.4, 4.4.4 and 4.5.4 give additional details and a 1.2 mm for 10 MeV and 4.3 mm for 20 MeV protons.
summary of the methods used to obtain the data in At these energies, however, errors may result from
this report. use of the kerma approximation near interfaces
(119) In the Monte Carlo method, the values of between tissues of widely differing composition and
energy, direction, and path length are randomly density (e.g., at bone surfaces) and in calculation of
chosen from probability distributions. The particle operational quantities at shallow depths.
history is then established through the medium of (124) In the case of infinitesimally small regions,
the phantom as the particle undergoes various inter- such as those that occur in the definition of the
actions and ends when the particle becomes ab- operational quantities, numerical methods are used
sorbed, leaves the region of interest, or no longer has to calculate the limiting value of the quantity. In
significant energy. calculating the energy fiuence entering the volume,
it is necessary to include all types of particles

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resulting from secondary and tertiary processes,I5 in
3.4.2. Transport codes: general features and addition to the primary radiation. For external irra-
special codes diation by photons at the energies considered in this
report, the secondaries of concern will be photons
and electrons. For neutron irradiation, the secondar-
General features of the transport codes ies of concern are protons and heavier charged
(120) The general Monte Carlo technique provides particles, photons, and electrons. At high energies,
a computational framework for the description of an all radiations produce a complex radiation field by
analogue technique for the solution of radiation electromagnetic and hadronic cascades (Bertini, 1969;
transport problems. By this 'classical analogue tech- Kalinovskii et aI., 1989).
nique,' all the individual interaction processes of (125) Calculation of the transport of charged radia-
each particle history are followed. It is possible with tions is both complex and time-consuming. Fortu-
this technique to consider tracking the interactions nately, for those radiations and energies considered
of individual particles in their passage through in this report, the transport of charged particles may
matter and to obtain absorbed dose distributions by be facilitated by means of the CSDA, which assumes
tracing many particle histories. But even with the that the slowing down of electrons is a smooth
availability of high-speed digital computers and gen- process as a function of energy, yielding the concepts
eral Monte Carlo codes (which also facilitate the of projected ranges and stopping power.
calculation of radiation transport in complex geom- (126) Provided that the range of the charged
etries), this approach makes heavy demands on secondaries is small with respect to the extension of
computer time. Variance reduction techniques are the volume considered, one may evaluate the ab-
used to reduce this demand (Spanier and Gelbard, sorbed dose by means of the kerma approximation,
1969; Lux and Koblinger, 1991). i.e., by multiplying the incident fiuence by the appro-
(121) Several adaptations of the general Monte priate kerma coefficients. I6 The kerma approxima-
Carlo technique have been developed to allow for tion is always justified if charged-particle equilib-
different interactions of charged and uncharged par- rium exists.
ticles. In addition, approximations to the description (127) The dose to the bone surface (a very thin
of some ofthe atomic and nuclear processes [e.g., the (- 10 pm), soft tissue layer enveloping the bones) is,
continuous slowing-down approximation (CSDA)] or in practice, replaced by the mean dose in bone. Thus,
the kerma approximation may have been used. the dose enhancement occurring at the bone surface
(122) The mean absorbed dose in a defined volume due to an increased production of secondary elec-
of material may be computed from the incident and trons in bone vis a vis soft tissue is of reduced
emerging energies from the volume by dividing this significance. For photon energies below approxi-
'energy imparted' (see ICRU Report 51 for a full mately 300 keV, the effect of this replacement is
definition) by the mass ofthe volume of material.
(123) For calculation of mean organ doses, the 15 For brevity, these are referred to as 'secondary radiations' or

dimension ofthe volumes considered is in most cases 'secondaries.'


16 To be consistent throughout this report, the term 'kerma
sufficiently large that use of the kerma approxima-
coefficient' is used rather than the more familiar term 'kerma
tion is acceptable for photon energies up to 3 MeV factor.' This convention wa s adopted to reserve the description of
and for neutrons up to 20 MeV. For photons, Drexler 'factor' for quantities that h a ve no physical dimensions (see
et al. (1989a) found agreement within 5% for organ Section 4). 17
more than compensated for by the fact that the since its first operation (Ford and Nelson, 1978). The
absorbed dose in bone is much higher than that in following briefly describes the two recent versions:
soft tissue (due to the higher attenuation coefficient EGS4(*) Code. The general-purpose EGS4 code
of bone) and is still a conservative estimate for the has been used in the version described by Nelson et
enhanced dose to the adjacent soft tissue layer al. (1985). In this code, Moliere multiscattering
(Drexler, 1968). Above 300 keV, the attenuation theory is used and a simple treatment of the photon
coefficients of bone and soft tissue differ by not more transport is applied (Moliere, 1948). More details of
than 5% and approximate secondary electron equilib- the operation of this code can be found in Hirayama
rium is established. For neutrons up to 20 MeV, dose (1994).
calculations have always been performed applying EGS4(**) Code. An improved version of the
the kerma approximation. Because of the short EGS4(*) code has been tested and implemented (Ma,
range of the recoil protons and heavier charged 1992). The main modifications to this version are as
particles, the errors in the absorbed dose data re- follows:
main small. • provision for a new algorithm, which enables
(128) Electrons undergo many more interactions better treatment of low-energy electron trans-
along their path than do uncharged particles such as port;

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photons or neutrons. Electron interactions may be • use of correlated sampling, yielding better effi-
described in terms of stopping power, range and ciency and accuracy of calculation in many cases;
range-straggling. This description enables the com- • implementation of the code on parallel comput-
putation-time for electron transport calculations to ers; and
be reduced using the 'condensed history' (or 'path- use of a photon-interaction forcing method.
segment') concept. In this technique, the particle (132) ETRAN (electron transport) is a 'condensed-
paths are divided into path segments, along which history' type Monte Carlo code (Seltzer, 1991) in
many elastic and inelastic Coulomb collisions occur. which the collision energy losses in each short path
This allows for treatment of the combined effects of segment are sampled from a Landau distribution,
many collisions occurring along each path segment, which incorporates Blunck-Leiseegang binding cor-
without having to sample a very large number of rections, in conjunction with the stopping powers
individual interactions. Energy losses are accounted given in ICRU Report 37 (ICRU, 1984). The sam-
for using the CSDA and energy-loss-straggling distri- pling of angular deflections obeys the Goudsmit-
butions; angular scattering is accounted for using Saunderson multiple-scattering distribution based
multiple-scattering distributions. For a basic discus- on the screened Mott single-scattering cross sec-
sion of these topics see Berger (1963) and Andreo tions, recently revised to match recent transport
(1991). cross sections (Berger and Wang, 1987). Radiative
(129) During the last decade, several codes used to energy losses are sampled along each path segment
calculate the transport of electrons and photons in according to bremsstrahlung cross sections (Seltzer
matter have been made available, many of which are and Berger, 1986) and knock-on electron production
continually being improved. Although some differ- is treated through the Muller theory. Conventional
ences are apparent in the electron transport algo- analogue Monte Carlo techniques are used to follow
rithms ofthese codes (e.g., in the detailed treatment the bremsstrahlung histories and photon interac-
of energy losses by primary electrons and the produc- tions are sampled on the basis of cross-section data
tion of bremsstrahlung photons and knock-on elec- given in Berger and Hubbell (1987). ETRAN is able
trons), the estimates of the absorbed dose obtained to treat the transport of electron-photon cascades
are generally in good agreement (see Section 4.3.3). with energies from the Ge V region down to 1 keV. In
order to extend the field of application of ETRAN to
complex three-dimensional geometries, several
Descriptions of various transport codes
ETRAN-based codes have been successively devel-
(130) DEEP (Yamaguchi, 1991) is a computer code oped: ZTRAN, ZEBRA, SANDYL, ACCEPT. These
(see Section 4.3.3), which incorporates the Monte codes have been reorganised in the Integrated Tiger
Carlo code MORSE-CG (Emmett, 1975) (see below, Series (ITS). The most recent version is Version 3.0
Paragraph 140). DEEP has the capability to calcu- (Halbleib et al., 1992). ITS Version 1.0 has recently
late effective dose and the equivalent dose to 60 been incorporated into the neutron/photon transport
tissues of an adult modified-MIRD-phantom for pho- code MCNP (Briesmeister, 1993), now referred to as
tons in the energy range 6.2 keV to 12 MeV. In the MCNP-4A.
calculations of absorbed dose, kerma coefficients are (133) FANEUT is a Monte Carlo code specially
generated from the data of Storm and Israel (1970) developed for calculation of the characteristics of the
and Hubbell (1982). absorbed dose from neutrons and secondary photons
(131) EGS4 Code. The electron-gamma shower in tissue-equivalent materials (Kurochkin, 1994). A
18 (EGS4) code has been continually improved ever one-dimensional geometry that can treat slabs and
spheres is used, and the anisotropy and kinematics particle cross sections needed to perform transport
of elastic neutron scattering are approximated by a calculations are produced by the code itself using
fifth-order Legendre polynomial expansion. Inelastic intranuclear cascade calculations combined with
scattering is treated using group cross sections. For evaporation models having a 'pre-equilibrium inter-
thermal neutrons, a gas model combined with experi- mediate stage.' The code permits the transport of
mental cross-section data for hydrogen in water is neutrons, photons, and light nuclei up to 4He.
used (Biskpchuk et ai., 1987). (139) MCNP Code. The general-purpose code,
(134) GSF-National Research Center for Environ- which was developed at the Los Alamos National
ment and Health Code. The GSF code was originally Laboratory, can be used in complicated three-
designed at Oak Ridge National Laboratory under dimensional configurations for problems of radiation
the name ALGAM (Warner and Craig, 1968) and transport. Continuous improvements have been made
further developed at the GSF (Kramer, 1979; Veit et to this code. The new versions facilitate electron
ai., 1989). This code computes the dose deposited by transport calculations.
photons from an external or internal source in MCNPE-BO Code. The MCNPE-BO code con-
various sections of a different media phantom ap- sists of the MCNP-version 3A code (Briesmeister,
proximating the human body. The phantom could be 1986), which was modified to include the transport of

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either MIRD-type, voxel type, or simple sphere or electrons (Guaraldi and Padoani, 1994a,b). Moliere
slab. The code is based on the fractional photon multiscattering theory was implemented, with addi-
technique. Energy is deposited at the point ofinterac- tional correction tables intended to improve the
tion (kerma approximation) for the MIRD-type phan- stability of the results for low-energy electrons (Fer-
toms, and a correction for secondary electron effects rari and Guaraldi, 1992; Gualdrini and Padoani,
in the skeleton is applied. nd).17
(135) HADRON, a Monte Carlo code designed to MCNP4 Code. This latest version of the MCNP
calculate hadron-cascade transport in complex hy- code (Briesmeister, 1991) permits calculation of the
drogenous media (Golovachik et ai., 1989), is based transport of photons, neutrons, and electrons in very
on the cascade-exciton model of inelastic nuclear complex geometries. Goudsmit-Saunderson multi-
interactions. The yields of n, p, 7T± , 7T at the cascade
O
scattering theory is applied (Goudsmit and Saunder-
stage of the inelastic interaction and the yields of n, son, 1940; Landau, 1944), and detailed treatment of
p, D, T, 3He, a, and recoil nuclei at the de-excitation electron-scattering physics permits the transport of
stage are taken into account. The hadron-hydrogen electrons down to 1 keV.
cross section used is obtained by intranuclear cas- (140) MORSE-CG Code. The MORSE code (Em-
cade calculations. mett, 1975), one of the first Monte Carlo transport
(136) HL-PH Code. Basic information on this codes to be widely distributed, incorporates a reason-
Monte Carlo neutron transport code created by ably comfortable combinatorial geometry capacity.
Hollnagel may be found in Hollnagel (1990). This To shorten running time, this code uses group cross
code treats neutrons and photons, and uses standard sections but with one disadvantage: it limits the
Monte Carlo methods (with some variance-reduction capability to treat problems in which detailed struc-
techniques) and combinatorial geometry. The cross ture in the cross sections (such as resonances) is
sections are based on ENDFIBIV or later versions. important. Furthermore, preparation of group cross
The phantoms modelled by the code are identical to sections with a sufficient number of thermal groups
those used by Kramer et ai. (1982) and Williams et is not a trivial task. This is particularly true when
ai. (1985a). radiation transport is calculated in complex materi-
(137) JEUNESSE is a computer code used by als (e.g., anthropomorphic phantoms) and when it is
Yamaguchi (see Section 4.3.3) that incorporates the necessary to compute separate group cross-section
Monte Carlo code MORSE-CG (Emmett, 1975) (see sets for significantly different tissues such as muscle
below, Paragraph 140). JEUNESSE incorporates the or bone (see also DEEP and JEUNESSE).
age-specific phantoms designed by Cristy and calcu- (141) PTBIBG Code. Information on the Monte
lates organ equivalent doses and effective doses in Carlo transport code created by Grosswendt may be
models corresponding to 0-, 1-, 5-, 10- and 15-year found in a series of publications (Grosswendt and
olds, and adults (see also DEEP). Roos, 1986; Grosswendt, 1993, 1994a). This code
(138) LAHET Code (Los Alamos high-energy trans- uses the condensed history model described by Berger
port code). This code system is a modified version of (1963) and applied in previously mentioned codes.
the high-energy transport code (HETC), which was Developments by Nahum (1976) and Andreo and
originally developed at Oak Ridge Laboratories and
subsequently modified at Los Alamos. Basic details
of the code may be found in Prael and Lichtenstein 17 Throughout the text, the symbol 'nd' stands for 'not dated' and
(1989). The geometric capability incorporated in the indicates that the material ha s been made available to the Task
code is that of the MCNP code. The high-energy Group during its preparation and prior to publication. 19
Brahme (1984) are incorporated in the latest version
of the code. Using Moliere multiscattering theory
AP PA
and Landau energy-Ioss-straggling distribution, the
energy degradation is treated within the framework ISO
of the CSDA and combined with other corrections
and approximations described by Rohrlich and Carl-
j I
~
son (1954) and Sternheimer et al. (1984). To obtain
adequate spatial detail of the electron depth-dose
curve, the phantom material is subdivided into
planar slices, each having a thickness of 0.05 r o,
where ro is the CSDA range for the primary electron
energy. This is a very similar technique to that used
with the ETRAN code (Seltzer, 1991). Near the
phantom surface where the dose gradient is large, an
accurate description of the energy deposition is
obtained by modelling thinner additional slices, thus

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enabling a more accurate determination of the flu-
ence to dose conversion coefficients.
(142) SAM-CE Code. Basic information on this
neutron transport code, which uses combinatorial
geometry and a variety of special variance-reduction
methods, is given by Lichtenstein et al. (1979). In
recent years, this code has been increasingly re- LAT
placed by the MCNP and/or LAHET code, both of Fig. 5. Some irradiation geometries of an anthropomorphic
which are maintained and distributed by the Radia- phantom.
tion Shielding Information Center at Oak Ridge.

etries when warranted. Where there are only small


3.5. Irradiation Geometries
differences in the absorbed dose between these two
geometries, data are presented as an average of the
3.5.1. General
RLAT and LLAT values.
(143) Because the number of conceivable geom- Rotational geometry (ROT). The geometry in
etries in which the human body might be irradiated which the body is irradiated by a parallel beam of
is virtually limitless, it has become conventional to ionising radiation, from a direction orthogonal to the
limit, somewhat arbitrarily, the number of irradia- long axis ofthe body, which rotates at a uniform rate
tion geometries for which calculations are per- around the long axis. Alternatively, this geometry
formed. In general, calculations are carried out may be defined by rotating the body at a uniform rate
assuming whole-body irradiation by broad unidirec- about its long axis, while irradiating the body by a
tional or plane-parallel beams. Following is a descrip- broad beam of ionising radiation from a stationary
tion of some typical irradiation geometries, which source located on an axis at right angles to the long
are shown schematically in Fig. 5. axis of the body.
Antero-posterior geometry (AP). The irradia- Isotropic geometry (ISO). Defined by a radia-
tion geometry in which the ionising radiation is tion field in which the particle fluence per unit of
incident on the front of the body in a direction solid angle is independent of direction.
orthogonal to the long axis of the body. (144) Although the geometries defined above are
Postero-anterior geometry (PA). The irradia- idealised, they may be taken as approximations to
tion geometry in which the ionising radiation is actual conditions of exposure. Thus, for example, the
incident on the back of the body in a direction AP, PA, and LAT geometries are considered to ap-
orthogonal to the long axis of the body. proximate radiation fields produced by single sources
Lateral geometry (LAT). The irradiation geom- and particular body orientations. In contrast, the
etry in which the ionising radiation is incident from ROT geometry is seen as an approximation to irradia-
either side of the body in a direction orthogonal to tion from a widely dispersed planar source (e.g., as
the long axis of the body. When it is necessary to be would be likely from environmental contamination).
more specific, the following symbols are used: RLAT This approximation results in radiation incident at
(from the right side to the left side of the body) or right angles to the long axis of a person standing or
LLAT (from the left side to the right side ofthe body). walking about in the field. The ROT geometry may
In this report, results of the calculations are pre- also approximate that of a person who moves ran-
20 sented separately for the LLAT and RLAT geom- domly in the radiation field of a single source irradi-
ating at right angles to the long axis ofthe body. The (147) In practice, because of the definition of the
ISO geometry would be approximated by a body directional dose equivalent, H'(d,{l), dose equiva-
suspended in a large cloud of radioactive gas. This lents at depths, d, along the principal axis are
geometry is often assumed for irradiation by natural calculated for various angles incident between 0°
radionuclides in homes or the environment, or by and 90° to the principal axis of the sphere. (For a
atmospheric releases of radionuclides into the envi- discussion ofthe correlation between the value ofthe
ronment. angle ex and the irradiation geometry see Section
(145) Irradiation geometries that more accurately 2.6.3).
describe practical situations, other than those previ-
ously described, may be defined. These may include
irradiation by broad unidirectional or plane-parallel 3.5.3. Geometries used with the ICRU slab
beams that are not perpendicular to the long axis of
the body, beams that may be either divergent or (148) In calculations of dose distributions in the
convergent, and beams that are non-uniformly dis- ICRU slab phantom, a large number of incident
tributed across the body. radiation geometries can be assumed by varying the
angle of incidence at the face of the slab. Calcula-
tions have been made for photons, neutrons, and

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3.5.2. Geometries used with the ICRU sphere
electrons for radiation incident on the slab at various
(146) In calculations of dose distributions in the angles between 0° and 90°. It is also possible to
ICRU sphere phantom, the five (six if both lateral define the ROT and ISO geometries for the slab in a
geometries are counted) idealised irradiation geom- similar manner as defined for the ICRU sphere
etries described in Section 3.5.1 are generally used. phantom (see Section 2.6.3).

21
4. Conversion Coefficients

4.1 Introduction discussed in this report. These needed modifications


include
(149) A 'conversion coefficient' links the protection
• re-evaluation of cross-section data for higher
and operational quantities to physical quantities
energies and compilation in a format compatible
characterising the radiation field. In practice, the
with the codes;
physical quantities that are usually calculated or
• calculation of the energy transported by second-
used are the tissue-absorbed dose (D T ), air kerma
ary charged particles within the irradiated tis-
free-in-air (Ka ), and particle fluence (4)). Thus, for
sue.
example, the effective dose, E, may be related to the
fluence of particles by a conversion coefficient.
(150) The data reviewed by the Joint Task Group
4.2.1 Radiation energy spectra and mixed
were either available in the scientific literature or
radiation fields
generated by members of the Joint Task Group and
their colleagues. This section summarises the conver- (155) The reference conversion coefficients given

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sion coefficient data reviewed and recommends refer- in this report were calculated for irradiation by
ence sets of conversion coefficients whose use will monoenergetic radiation. In practice, monoenergetic
provide for a consistent approach to the interpreta- radiation fields are rare and generally the energies
tion of measurements in radiological protection. ofthe constituent particles extend over a wide range.
Even in standards laboratories, the reference fields
used for type tests and calibrations are often only
4.2 General
quasi-monoenergetic. The mean or effective conver-
(151) The two major purposes of this report are to sion coefficients for broad spectra must be deter-
present data that permit a general understanding of mined by integration over the entire radiation en-
the relationships between the protection and opera- ergy spectrum.
tional quantities, and to determine whether the (156) Furthermore, the radiation fields of practical
latter are adequate predictors of the former for importance in radiological protection usually consist
purposes of radiological protection in practical cir- of more than one type of radiation because of the
cumstances (e.g., in mixed radiation fields and for secondary radiations produced by the interaction of
broad energy spectra). the primary radiation. This is always true for neu-
(152) The particular values of the quantities pre- trons at any energy and is true for most other
sented in this section depend upon a large number of radiations at high energies.
parameters. An exhaustive discussion of all the (157) For mixed radiation fields, the separate
published data is beyond the scope of this report but contributions from all components of the radiation
representative data have been selected to illuminate field must be summed to determine the overall
general principles. Extensive references to the origi- conversion coefficients. For each component of the
nalliterature make it possible for those interested to radiation field, the mean conversion coefficient for
examine specific details. Based on the analysis of all that component must be determined by integration
the data available to the Joint Task Group, recom- over the entire radiation energy spectrum. These
mended reference data sets are given. calculations may be readily carried out by means of
(153) Data were reviewed for photons with ener- the conversion coefficients for monoenergetic radia-
gies up to 10 MeV, for neutrons 18 with energies up to tions presented in this section.
180 MeV, and for electrons with energies up to 45
MeV (see Tables 4-6). Calculations for photons,
neutrons, and electrons with higher energies or for 4.3. Conversion Coefficients for Photons
other radiations that incorporate the new recommen-
dations of ICRP in Publication 60 are either sparse 4.3.1. Introduction
or have not yet been performed.
(158) This section provides reference conversion
(154) Modifications to existing transport codes,
coefficients from air kerma free-in-air and from
and their supporting databases, will be necessary to
photon fluence to both protection quantities and
extend calculations to energies higher than those
operational quantities. The protection quantities
considered are the tissue or organ 19 absorbed dose,
18 The neutron data above 30 MeV are limited. Seven groups of
authors provided organ dose and effective dose data for neutron
energies up to 20 MeV. Five groups of authors have published
calculations of operational quantities but of these only two sets 19 The expression 'tissue or organ' is often abbreviated to 'organ'
22 extend above 30 MeV. in this Section.
TABLE 4. - Summary of calculations of the conversion coefficients for protection quantities for photons ...,'"
.:
.~
Codes!databases! Protection Energies No. of u
anthropomorphic quantities Irrad iation or energy energy IEQ)
Authors models calculated (DT , E ) geometries ra nge points 0
U
Yamaguchi (1991); Monte Carlo code: E and values of DT cal- Horizontally and verti- 45 keV, 90 keV and 1.25 3 .:0
Yamaguchi and DEEP (Yamaguchi, culated for selected cally varying angles MeV '0...0
Q)
Yoshizawa (1991, 1991) organs
1992) Physical data:
.:>0
U
Hubbell (1982)
Model:
MIRD (hermaphrodite)
Yamaguchi (1994b) Monte Carlo code: Both E and DT calcu- AP 17 keV to 8.5 MeV 12
JEUNESSE (Ya magu- lated PA
chi,1992 ) RLAT
Physical data: ROT
Hubbell (1982) ISO
Models:
0, 1,5, 10, 15 year old;
Adult (hermaphro-

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dite); (Cristy, 1980)
Reece et al. (1993) Monte Carlo code: No values for E : values AP 80 keV, 300 keV, 1 MeV 3
MCNP of DT calculated for PA
Physical data: nil selected organs LLAT
Models: RLAT
MIRD (male & female)
Zankl et al. (1992, 1997, Monte Carlo code: Both E and DT calcu- AP 10 keV to 10 MeV 17
nd (a,b]) GSF Code (Kra mer et lated PA
al., 1982) LLAT
Physical data: RLAT
DLC99IHUGO (ENDF/ ROT
B-V (Roussin et al., ISO
1983)] Horizontally and verti-
Models: cally varying angles
ADAM and EVA (adult models and
(Kramer et al., 1982); selected energies
BABY/CHILD (Veit et only)
al., 1989)

D T , and the effective dose, E. The operational quanti- the organ absorbed dose per unit air kerma (Gy/Gy)
ties given are ambient dose equivalent, H * (d ), the is numerically equal to the organ equivalent dose per
directional dose equivalent, H'(d) , and the personal unit air kerma (Sv/Gy). Thus, the conversion coeffi-
dose equivalent, Hp(d). The conversion coefficients cients are presented in terms of the organ absorbed
provided are for irradiation by monoenergetic pho- dose per unit air kerma (Gy/Gy) for photons. The
tons incident upon calculational models or phantoms conversion coefficients for the effective dose and
of interest and for several irradiation geometries. operational quantities are given in units of (Sv/Gy).
The general methods used to calculate these conver- In addition, so that the conversion coefficients for
sion coefficients are described in Section 3. photons may also be presented in a manner consis-
tent with those for neutrons and electrons (i.e., in
terms of particle fiuence), and to provide as complete
4.3.2. Special considerations for photons
a database as possible for a variety of calculational
(159) In this report, most of the conversion coeffi- purposes, the data can be transformed into conver-
cients for photons are presented in terms of the sion coefficients per unit photon fiuence using the
quotient of a protection or operational quantity to air information in Table A.1 of Annex 2.
kerma free-in-air expressed in units of either (Gyl
Gy) or (Sv/Gy). Purists may object to the manner in
which the units of the conversion coefficients are 4.3.3. Methods of calculation
expressed since the unit (Gy/Gy) or (Sv/Gy) is strictly
dimensionless. Nevertheless, the Commissions
thought it would be helpful if the dimensions were
Computer codes
expressed in this way to add clarity to the text and
data provided. For photons, the numerical value of (160) General features ofthe transport codes used
the radiation weighting factor is one (WR = 1) and for photon calculations are discussed in Section 23
TABLE 5. -Summary of calculation of the conversion coefficients for protection quantities for neutrons
Codes/databases! Protection quantities Energy No. of energy
Authors models calculated (DT , H T , E ) Geometries range points

Morstin et at. (1992) Monte Carlo code: All AP Thermal to 20 MeV 33


MCNP PA
Neutron cross sections: LLAT
ENDFIB-IV (calculated) RLAT
Model:
EVA
Nabelssi and Hertel (1993b) Monte Carlo code: All AP 10 MeV to 19 MeV 14
MCNP PA
Neutron cross sections: LLAT
ENDFIB-V & RMCCS-MCNP RLAT
Kenna coefficients: ROT
Caswell et al. (1980)
Model:
PNL (male, female)
Leuthold et at. (1992) Monte Carlo code: All AP 10 eV to 13.5 MeV 14

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SAM-CE PA
.S Neutron cross sections: LAT
ENDFIB-IV ROT
Kenna coefficients:
ICRU 26 (1977)
Model:
ADAM and EVA
Leuthold et al. (nd) Monte Carlo code: All AP Thermal to 20 MeV 19
MCNP PA
Neutron cross sections: LLAT
ENDFIB-IV RLAT
Kerma coefficients: ROT
White et al. (1992) ISO
Model:
ADAM and EVA
Yamaguchi (1993, 1994c-d) Monte Carlo code: All AP Thermal to 18.3 MeV 16
JENDL-3 PA
Kenna coefficients: RLAT
Caswell et al. (1980) ROT
Model: ISO
MIRD
Stewartetal. (1993) Monte Carlo code: All AP 1 keV to 20 MeV 17
MCNP PA
Neutron cross sections: LAT
ENDFIB-F
Kenna coefficients:
Caswell et al. (1980)
Model:
PNL (male, female)
Hollnagel (1990, 1992, 1994a) Monte Carlo code: All AP Thermal to 20 MeV 32
HL-PH PA
Neutron cross sections: LAT
ENDFIB-IV ROT
Kerma coefficients: ISO
Caswell et al. (1980 )
Model:
ADAM and EVA

3.4.2. Several different codes were used to calculate JEUNESSE (Yamaguchi, 1992) to calculate 'age-
the data reported here. Zankl et al. (1992, 1997, nd) dependent' effective doses (Yamaguchi, 1994b). Both
used a Monte Carlo code written by Kramer et al. DEEP and JEUNESSE incorporate the Monte Carlo
(1982) for the calculation of organ equivalent doses code MORSE-CG (Emmett, 1975). Reece et al. (1993)
and effective doses for adults and for two pediatric used the MCNP computer code (Briesmeister, 1986)
models. Yamaguchi and Yoshizawa (1991, 1992) and to calculate organ equivalent dose conversion coeffi-
Yamaguchi (1991) used the DEEP Monte Carlo code cients. Aspects of the use of the kerma approxima-
to calculate the effective dose for adult models. These tion and its limitations in these calculations are
24 latter authors also used the computer code discussed in detail in Section 3.4.2.
TABLE 6. -Summary of calculations of the conversion coefficients for operational quantities for neutrons
Operational quantities calculated Energy No. of energy
Authors Codes/databases H*(lO) H'(10,()() range points

Sannikov and Savitskaya (1993, nd) Monte Carlo code: Yes No No Thermal to 5 GeV 21
HADRON; FANEUT
Neutron cross sections:
HADRON
Kerma coefficients:
Caswell et al. (1980)
Nabelssi and Hertel (1993a, 1994) Monte Carlo code: Yes No No 1 keV to 180 MeV 30
HMCNP
Neutron cross sections:
ENDF/B-IV and RMCCS-MCNP
Kerma coefficients:
rCRU 26 (1977)
Leuthold et al. (nd) Monte Carlo code: Yes No No Thermal to 30 MeV 32
HL-KUQU
Neutron cross sections:

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ENDF/B-IV
Kerma coefficients:
Caswell et al. (1980)
Hollnagel (1994b) Monte Carlo code: Yes 0°:5 Ci :5 180° 0° :5 Ci :5 75° Thermal to 19 MeV 33
HL-KUQU
Neutron cross sections:
ENDF/B-IV
Kerma coefficients:
Caswell et al. (1980)
Schuhmacher et al. (1994); Monte Carlo code: Yes 0°:5 Ci :5 90° 0°:5 Ci :5 90° Thermal to 20 MeV 61
Siebert and Schuhmacher MCNP
(1994); Siebert et al. (nd) Neutron cross sections:
ENDF/B-V
Kerma coefficients:
Caswell et al. (1980)

Models and phantoms (Knight and Roussin, 1983; Roussin et al., 1983).
Yamaguchi and Yoshizawa (1991,1992) and Yamagu-
(161) For calculations corresponding to adults,
chi (1994a) used kerma coefficients from Hubbell
Zankl et al. (1992, 1997, nd) used male and female
(1982).
adult mathematical models (Kramer et al., 1982)
derived from the MIRD phantom (Snyder et al.,
1969, 1978). Reece and co-workers (1993) also used a Summary
modified MIRD phantom to obtain their data while
(164) Table 4 summarises the computer codes,
Yamaguchi and Yoshizawa (1991, 1992) and Yamagu-
physical databases, anthropomorphic models, and
chi (1994a) used a hermaphrodite modified adult
irradiation geometries used by each group of au-
MIRD phantom for their calculations of angular
thors.
dependence ofthe effective dose.
(162) For the investigation of the age dependence
of conversion coefficients for the effective dose 4.3.4. Available data
Yamaguchi (1994b) used hermaphrodite 0-, 1-, 5-,
10-, and 15-year-old child and adult anthropomor-
Protection quantities
phic mathematical models of different body sizes
designed by Cristy (1980). Zankl and her colleagues (165) The Joint Task Group reviewed organ dose
(nd) used tomographic models of an 8-week-old baby data calculated by three groups of authors. These
and a 7-year-old child based on whole-body com- three groups were Reece at Texas A and M Univer-
puted tomographic data of actual children (Zankl et sity (Reece et al., 1993), Yamaguchi and his collabora-
al., 1988; Veit et al., 1989). tors at JAERI (Yamaguchi and Yoshizawa, 1991,
1992; Yamaguchi, 1994a,b), and Zankl and co-
workers at GSF (Zankl et al., 1992, 1997, nd). Organ
Physical data
equivalent doses and effective doses for monoener-
(163) Zankl et al. (1992, nd) used photon cross- getic photons incident in broad parallel beams or
section data from the DLC-99/HUGO package incident isotopically on human models were pro- 25
vided (see Table 4). The irradiation geometries for large organs (e.g., lungs, liver, stomach). For organs
which calculations were made were antero-posterior or tissues distributed throughout the body (skin,
(AP); postero-anterior (PA); left and right lateral bone-surface, bone-marrow) the coefficients of varia-
(LLAT and RLAT) and the average of left and right tion were less than 1%. For smaller organs (e.g.,
lateral incidence (LAT); a 360 0 rotation about the testes, ovaries, thyroid), the coefficients of variances
model's longitudinal axis (ROT) and irradiation by a tended to be higher but only exceeded 15% at low
radiation field in which the particle fluence per unit energies (below approximately 30 keY) where the
solid angle is independent of direction (ISO) (see conversion coefficients are very small and thus the
Section 3). Some of the authors presented data for significance of this statistical uncertainty (for ex-
additional angles of photon incidence (Yamaguchi ample, in its impact on the uncertainty in the
and Yoshizawa, 1992; Zankl et al., 1997) and for estimate of effective dose) is low.
human models of different sizes (ages), (Yamaguchi, (168) It is difficult to estimate the uncertainties
1994b; Zankl et al., nd. introduced by the simplifications of the modelling of
the radiation transport, when compared to the physi-
cal phenomena occurring in reality. Comparisons of
Operational quantities
measured and calculated doses in phantoms and

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(166) No new data for the operational quantities models of simple geometry (e.g., the ICRU sphere or
are presented in this report but data for the ambient slab phantoms) and in an Alderson-Rando phantom
dose equivalent, directional dose equivalent, and indicate that these deviations are generally below
personal dose equivalent are taken from ICRU Re- 5-10%, and that they do not exceed 15% (Selbach et
port 47 (lCRU, 1992a) and ISO Report DIS /4037-3 al., 1985; Williams et al., 1985b; Grosswendt, 1989;
(ISO, nd) (see Paragraphs 188-196). No data are Veit et al., 1992). This conclusion is to some extent
available for Hp(d) in the body, but conversion coeffi- also confirmed by the fact that the data analysed for
cients for Hp,slab and Hp,thymus are used as surrogates this report, which were calculated using indepen-
for Hp in the human torso (see Paragraph 322). dent, different Monte Carlo codes and databases, in
most cases agreed to within the statistical uncertain-
ties given by the authors. As an example of the
Analysis of the variability of the data
agreement between the data from different authors,
(167) The statistical uncertainties of the calcu- Fig. 6 compares calculations of conversion coeffi-
lated organ equivalent dose conversion coefficients cients for effective dose by Yamaguchi (1994b) and
depend strongly on the photon energy, the size of the Zankl et al. (1997). When it was possible to compare
model, the location of individual organs and their data between several authors, there was general
volume. At photon energies above 17 keY the coeffi- agreement within the statistical uncertainties cited
cients of variation were generally less than 2.5% for (organ equivalent dose conversion coefficients for

..
::l
as

"0
11.1

<Xl .::...."
0> 0
0>
,...; ....
"
....
1:-- '-l

.
..,
10

0
Q..

~
0p:::
::2
0.10 1.00 10.00
Photon energy (MeV)
Fig. 6. Comparison of effective dose conversion coefficients for photons. Ratio of data from Yamaguchi (1994b) to data from Zankl et al.
26 (1997) is shown as a function of photon energy for five irradiation geometries.
adults from Reece et al. , 1993 and Zankl et al., 1997, set of organ equivalent dose data is shown graphi-
and effective dose conversion coefficients for adults cally in Annex 1 and compiled in tables in Annex 2.
from Yamaguchi and Yoshizawa, 1992, Yamaguchi, (171) The calculation of effective dose from the
1993, 1994b, and Zankl et al., 1992, 1997). Differ- data for the individual organ equivalent doses has
ences (up to about 20%) between the effective dose been described in Section 2.5.3.
conversion coefficients for adults from the data of (172) The reference values for conversion coeffi-
Yamaguchi and Zankl and co-workers are mainly cients for organ equivalent dose given in the Annexes
due to the different human models used in the are taken from the work ofZankl et al. (1997). Where
calculations and occur at low photon energies. comparisons are made between the data calculated
Whereas Yamaguchi used a hermaphrodite model, by Zankl and co-workers, and the data of other authors,
the data of Zankl and co-workers were calculated good agreement is observed (see Paragraph 167).
using female and male models. The smaller body size (173) Tables A2-A16 in Annex 2 give the refer-
of the female model resulted in higher organ dose ence conversion coefficients recommended by the
conversion coefficients, particularly at low photon Commissions for those specific organs for which the
energies. ICRP recommends tissue weighting factors [i.e., the
bladder; bone (red marrow); bone (surface); breast;

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colon; gonads (ovaries, testes, and the average value);
4.3.5. Conversion coefficients and analysis liver; lung; oesophagus; remainder; skin; stomach
and thyroid]. Table A13 in Annex 2 gives the refer-
Protection quantities: organ ence conversion coefficients for the remainder that
are calculated from data for those separate organs
and tissue doses and tissues (adrenals; brain; kidney; muscle; pan-
(169) In the analysis of the various sets of organ- creas; small intestine; spleen; upper large intestine;
dose data, principal attention was devoted to those thymus; and uterus) that make up the remainder as
organs and tissues, including those that make up the defined in ICRP Publication 60 (see Section 2.5).
'remainder', by which ICRP specifies effective dose With two exceptions (the thymus and the uterus),
and for which weighting factors are specified in separate tabulated data are not given for the organs
ICRP Publication 60. of the remainder but these may be obtained from the
(170) Figure 7 shows organ equivalent doses for a work ofZankl et al. (1997) if required.
few selected organs. The curves show organ equiva-
lent doses per unit air kerma free-in-air (Sv/Gy) in
Protection quantities: effective dose
AP irradiation geometry as a function of photon
energy for the colon, female breast, lenses of the (174) Table A17 summarises the reference conver-
eyes, lungs, red bone marrow and skin. A complete sion coefficients for the effective dose per unit air

skin
breast
...... .
·. ....
red bone marrow
os
e~ 1.5
:
:' /
-,'. ...:;..
colon
lungs

.
.:.:
~
:/' /.' ..... ".;.;..
.' ............... '-..,.,.,. eye lenses

...'c
;
I·:.
/: .'/ ". .........
"". ......... ""'"........-.
::I I .... . . . .. ..:..::.-..:.:::::.:. ':: ::.:-::.:.:: ':.:..:.-:.::.. .::.....
t
Q.
1.0
I
I
; ---
- - ;-:.. ....
~----------
Cl
------
..
ID
o
"'"
cCl
II ,
" I/
iii 0.5
I i I
> I .7 /
'S
tr
Cl
/ ;;-
.!'
C

o
..
os
bII
:i'
//
0 °;'" , "
/

0 . 10 1.00 10.00
Photon energy (MeV)
Fig. 7. Organ equivalent doses for selected organs inAP irradiation geometry as a function of photon energy. 27
kerma evaluated from the organ data provided in complex manner by several parameters, including
Annex 2. The results are shown graphically in Fig. 8. the photon interaction cross sections in tissue, the
(175) In the selection of reference data sets for location of the organs in the body, the tissue weight-
effective dose, the same procedure adopted in the ing factors for the individual organs that contribute
case for organ doses was used. Reference conversion to the effective dose, and the irradiation geometry.
coefficients for the effective dose values were taken (178) The energy dependence of conversion coeffi-
from those authors providing the most comprehen- cients for the individual organs is determined by the
sive data set for the respective parameters under energy variation of photon interaction cross section
consideration. This procedure resulted in the selec- and the location of the organ in the body. Above 10
tion of data from Zankl et al. (1992, 1997) for energy keV, the photoelectric cross section decreases with
dependence, Yamaguchi and Yoshizawa (1992) for energy and the conversion coefficients correspond-
angular dependence, and Yamaguchi (1994b) for age ingly increase due to the increasing predominance of
dependence. The data from Yamaguchi (1994a) and Compton scattering. The peak in the conversion
Zankl et al. (1997) for the adult models are in good coefficients seen between 80 and 100 keY, particu-
agreement (Fig. 6). The data for various ages
larly in the AP and PA geometries (Fig. 8; see also
(Yamaguchi, 1994b; Zankl et al., nd) show the best
Figs. A.1-A.19 in Annex 2), is due to the large
agreement for the LAT and ROT geometries with
proportion of large-angle scatters occurring in this

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somewhat larger differences, but still good agree-
energy region. This peak is especially evident for
ment, for the AP and PA geometries. The differences
superficially located organs where backscattering is
between the data sets observed for the ISO geometry
are probably due to different modelling of this geom- important but less pronounced for deeper lying
etry. organs. For these latter organs, the deeper penetra-
(176) The data-selection procedure described above tion of radiations with increasing energy is of greater
is believed not to introduce any inconsistency in the importance.
reference data because, when it was possible to (179) At energies above 100 keY, the conversion
compare those data common to several authors, coefficients for the superficial organs show a decline
there was general agreement within the statistical while those for the deeper organs show a small
uncertainties cited by the authors (see also Para- increase. Between 100 keY and 1 MeV, the total
graph 168). photon interaction cross section in tissue does not
change significantly with energy. At energies above
1 MeV, the pair-production cross section increases
Energy dependence of effective dose slowly with photon energy for the low atomic num-
(177) The energy dependence of conversion coeffi- bers typical of the constituents of tissue. At photon
cients for the effective dose (Fig. 8) is determined in a energies below 10 MeV, pair production is of little

1.5
,......"
>-
~
>
ell
---
~.

~
CIS
1.0
..........

./> . . . . . ::~:::::.: .........................::::.:::::.:.::::~.,..-...-..


E
4.l
...
.:.I
'a;
.... - ... _ ... -... ..-- ::::-~.~.,;::;:;.-=
....
'2
...:::s
: /
I ".-.........
......... --- - - - --
! / ,," - - - - - - - - - :.: ..........
--- -;:;'-.::",.-
-:. -:::~---:-.-.
00
a> 4.l
Q.
If / ,'/ .... -._._._._.-._.-.
a>
,....; 4.l 0.5 :!/ ,,,
r:
It:>
<I)
0 DI/
"0 AP
t:0 4.l ::1 "
PA
0- >
.::: il'; LLAT
Q) :/' I;
~
~ • l' RLAT
.~'L?
~ ,d./ ROT

-
tl.l
C,.)
0.0
~ . ISO

0.01 0.10 1.00 10.00


Photon energy (Me V)
Fig. 8. Reference conversion coefficients for effective dose for photons in various irradiation geometries on an adult anthropomorphic
28 computational model. Numerical data are given in TableA.17.
importance in determining the conversion coeffi- angles oriented from the left side than for those from
cients. the right side.
(180) The different forms ofthe energy variation of (182) These effects occur because many of the
conversion coefficients for effective dose with irradia- organs that are dominant in determining the magni-
tion geometry reflect the different locations of organs tude of the effective dose are located towards the
with respect to the incoming photon beam and the front of the body. When the body is irradiated in
value of their weighting factors. The 'back-scatter geometries other than the AP, these frontal organs
peak' is most evident in the AP irradiation geometry are shielded by thicker layers of tissue than is the
because those organs with a large weighting factor case for photon incidence from the front of the body
are anteriorly located. In the LAT irradiation geom- (see the data for the bladder, Fig. A.1; breast, Fig.
etry, the 'back-scatter peak' virtually disappears A.4; colon, Fig. A.5; gonads, Fig. A.8; liver, Fig. A.9;
because all the organs are more or less 'deep-lying' stomach, Fig. A. 14; and thyroid, Fig.A.15 in Annex 1).
from this aspect. (183) There is an inherent asymmetry that occurs
with respect to irradiation from the left- or right-side
of the body because the specification of the effective
Angular dependence of effective dose dose includes several unpaired organs that are not

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(181) Conversion coefficients for the effective dose symmetrically located with respect to the vertical
from air kerma are strongly dependent upon the midline of the body (see the data for the colon, Fig.
direction of the photon incidence. This is illustrated A.5; liver, Fig. A.9; oesophagus, Fig. A. 11; and stom-
in Figs. 9 and 10, which present conversion coeffi- ach, Fig. A.14 in Annex 1).
cients for three photon energies and a variety of (184) For vertically varying incidence (see Fig. 10),
incident angles. For horizontally varying incidence the conversion coefficients are again highest for
(see Fig. 9), the conversion coefficients are highest anterior and anteriorly oblique angles with a steep
for the anterior and anteriorly oblique angles, de- decrease towards irradiation from overhead or the
creasing for lateral incidence and increasing again ground-again showing an increase for posterior
for posterior and posteriorly oblique incidence. The and posteriorly oblique incidence. The reasons for
conversion coefficients are also higher for incident these variations are the same as those previously

left side
...... ....
.'. 1.25 MeV
. 90 keV
.......... '
, : ' '0 45 keV

•.••.•.•..l:E> ..•...•••:;._..:~: __
: ..... ... " .....
.: ..... .......
, \
'.
...

:''?\-.:>\\\
:>..,.": \ ;
\
\
\
\
'.
...
".
:
bock
\ :
front
'1:5
I :
I :
I ;
I :'
I
I
".....
' .-
..
~ -.~
.:...:'
-- '

'. .'
'0.:" ;"
.'
·······.1.5
right side
Fig. 9. The angular variation of effective dose for photons: effective dose per unit air kerma in free air, E / K., for monoenergetic parallel
photon beams incident at various angles on an adult anthropomorphic computational model. The direction of incidence is orthogonal to the
longitudinal axis of the body. 29
top
.. ·······,..5 ......
1.25 MeV

.......... :.... 90 keV


45 keV

. .....1:0 .....
., ..... :.,:....
" "
.......
". ,."
.,
: .....,
'.' ,,
:
:/ "" ,
it \ ':
I \ :
,; \ :
front
/1i5
I :
I :
I !
I :
/

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


",- -.':'

.:.(
--
·····1·.0
"

"
' ..:
········.1.5 ... ....
bottom
Fig. 10. The angular variation of effective dose for photons: effective dose per unit air kerma in free air, E / K., for monoenergetic
parallel photon beams incident at various angles on an adult anthropomorphic computational model. The direction of incidence is
orthogonal to the transverse axis of the body.

mentioned but enhanced because in this case, the and tissues for which the ICRP specifies tissue
shielding effect of the body is more pronounced. weighting factors) to the effective dose. In Figs.
13-15, the ratio wTHT/E is plotted as a function of
Age dependence of effective dose photon energy for the body irradiated in the AP, PA,
and ROT geometries. It is evident that at very low
(185) Yamaguchi (1994b) and Zankl et al. (nd) have energies (between 10 and 20 keV) those organs at, or
calculated the variation of effective doses with age close to, the surface of the body (with respect to the
(strictly, body size). Selected data from Yamaguchi direction of photon incidence) dominate the contribu-
(1994b) are shown in Figs 11 and 12 for the AP and tion to E. Above 20 keV, the relative contributions of
ISO geometries. The largest variation of the effective the superficial organs decrease and those of deeper-
dose with age was found for the LAT and ISO lying organs accordingly increase. At photon ener-
geometries. gies above approximately 1 MeV, the relative contri-
(186) Conversion coefficients for effective dose to butions of each organ approach the numerical values
air kerma decrease generally with increasing age. In of its respective tissue weighting factor, WT, because
the ROT geometry, for example, conversion coeffi- at these higher photon energies the organ dose
cients for 115 keV photons range from 1.10 to 0.91 Sv conversion coefficients, D~Ka, all tend to the value 1
Gy-l, respectively, for phantoms simulating ages Gy/Gy (see Figs. A. I-A. 15 in Annex 1). Figure 16
from newborn to the adult. The conversion coeffi- presents similar data in a somewhat different man-
cients for 510-keV photons range from 1.01 to 0.84 ner and shows the change in the relative contribu-
Sv Gy- l. The principal reason for this decrease is the tions of organ doses to the effective dose at photon
increasing amount of overlying tissue shielding the energies of 30 and 200 keV.
organs from the incident radiation with increasing
body size.
Operational quantities
Relative contribution of specific organs
(188) Conversion coefficients for the operational
and tissues to effective dose
quantities ambient dose equivalent, H*(d), and direc-
(187) Figures 13-16 summarise the relative contri- tional dose equivalent, H'(d), have been calculated
30 butions of specific tissues and organs (for all organs by several groups using Monte Carlo methods (see
!l
J:i
III
·8
~o
Co)
J:i
o
.~
III
>
J:i
o
Co)

o year
1 year
5 years
10 years
15 years

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


adult

0.0~ __~__~~~~u-__~__~~~~u-__~__~~~~~
0.01 0.10 1.00 10.00
Photon energy (MeV)
Fig. 11. Effective dose per unit air kerma free-in-air, E / Ka, for incident photons in AP irradiation geometry on anthropomorphic
computational models of various ages.

Section 3.4.2). Within their estimated uncertainties, Ambient dose equivalent


the coefficients calculated by these authors are in
(189) The conversion coefficients for the ambient
good agreement (Cross, 1989). The values of the
reference conversion coefficients for H*(10), H'(O.07) dose equivalent, H*(10), given in this report are
and H'(10) now recommended by both the ICRU and taken directly from ICRU Report 47 (ICRU, 1992a)
ICRP do not differ significantly from those previ- and are based on earlier evaluations of extant pub-
ously recommended in ICRP Publication 51 (ICRP, lished data by Wagner et al. (1985) and Grosswendt
1987) (see chapter 5). et al. (1988). Comparisons with the conversion coeffi-

......
>-
1.2
Q
>
til
'-' 1.0
~ .
tll
«S
§ O.B
~

....
..104

·a..
~

0.6

...='
~
Co.
~ 0.4
o year
'"0
"0 1 year
~ 5 years
.::: 10 years
u 0.2 15 years
....
~
Ul
adult

0.0
0.01 0.10 1.00 10.00
Photon energy (Me V)
Fig. 12. Effective dose per unit air kerma free-in-air E / K for incident photons in isotropic (ISO) irradiation geometry on
anthropomorphic computational models of various ages. ' a, 31
1.0000
".
.. :':.......... ". '"
.................................................................................. .
. . -x.,-:,"""--
~
I'. I
-:.=~~.;;-.::=·::;-:;..~~-:--= ..:::.·.7-:::~~.~~~:"'I
_ ... - ... - ... - ..
-'0 ./,/ "'--:- ......... - - - - - - - - - - ..
I f.• .' , _ -:~::.=..::::.::".:-_-:-.:-_:.::~~::..~...:.::-..:;.:.."!'":.:=::.n ....·... ~..'--·-
I / ''/'/ ; .?, ........... _ ... . ..... .
. /"
I I l~~:~?
"
"",,i
_· ,.
,.t....... " ...............-:-:-~
I "
.. ___~':..:''.:,:'',:, :".:. :':':":':'':':'':':'':':':':':.:....:,:...:,:...:... ::-..:-:.:.:..~..;'..:".:.:.....................1
gonad!!
1
~ colon
~' i lungs
, I ; red marrow
I }I slomach
I I I bladder
,! I breasl
I' I ' liver
,i I oesophagus
,i I remainder
I iI lhyroid
bone surface

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


. I
II skin
0.0001 LL_---'_-'--'-..L...J....L-I....L..1._ _........--'---'--'-.L-I-...........L-:--_-'-_L--I..-L-'-.o.....LJ:-':
0.01 0.10 1.00 10.00
Pholon energy (MeV)
Fig. 13. Relative contributions of specific organs to effective dose for incident photons in AP irradiation geometry on an adult
anthropomorphic computational model.

cients given in ICRP Publication 51 (lCRP, 1987) K a , for photon energies between 30 keV and 10 MeV
show that the three composite sets of data for H*(10) (lCRD, 1992a; Wagner et al., 1985). Values derived
are in good agreement and differ by less than 2% for from this formula are reproduced in Table A.21 of
photon energies up to 3 MeV and about 5% at 10 Annex 2 for those photon energies. Below 30 keV, the
MeV. values given in Table A.21 are based on the data
(190) Given this good agreement, the ICRD adopted given in ICRU Report 47 (lCRD, 1992a; see also
an empirical analytical function for calculation ofthe Grosswendt et al., nd; Hubbell and Seltzer, 1995).
numerical values of the conversion coefficient, H*(10)/ (191) When precise interpretation is required, it is

~!
.... ........... -.&, . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ... . . . . . . . . . . . . . . . . . . . . . .
oj
111
0
'1:1 -------------
t:
4l

.....~
U
4l
---
4l

....0
111 gonads
s:: colon
0
co
(j)
:;::: lunls
(j) ;:I red marrow
..... ,Q
slomach
t'-"
If:>
:5s:: bladder
breast
~ 0
u liver
0
~ oesophagus
4l
~ .....~III remainder
~
....
C) - 4l
CI:
thyroid
bone surface
skin
0.10 1.00 10.00
Photon energy (MeV)
Fig. 14. Relative contributions of specific organs to effective dose for incident photons in PA irradiation geometry on an adult
32 anthropomorphic computational model.
~
Q)
'0
~o
......
..................................................................................... U
~
,S
...
00
Q)

~
o
U

............................ , .
gonads
colon
I
lungs
red marrow
I stomach
I bladder
I breast

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


I liver
I oesophagus
remainder
thyroid
bone surface
skin
0.10 1.00 10.00
Photon energy (MeV)
Fig. 15. Relative contributions of specific organs to effective dose for incident photons in ROT irradiation geometry on an adult
anthropomorphic computational model.

recommended that interpolation between the values dependence factors are derived from the data of
of the conversion coefficients given in Table A.21 be Dimbylow and Francis (1989) and those in ICRU
carried out using a 4-point (cubic) Lagrangian inter- Report 47.
polation formula on a linear-log scale. For interpola- (194) Operational quantities at these two depths
tions of the angular distribution factors given in (0.07 and 10 mm) are used for monitoring weakly
Tables A. 22-A. 25 ofAnnex 2, a 4-point (cubic) Lagran- and strongly penetrating radiation, respectively. Val-
gian interpolation formula on a linear-linear scale is ues are not given for H'(3,ex) because this quantity is
recommended. not widely used in the routine practice for the
monitoring of photons. If the tissues at intermediate
depths (e.g., the lens of the eye) are likely to be
Directional dose equivalent
irradiated, they usually are protected by shielding
(192) The main source of the reference conversion (e.g., protective spectacles for the eye) and measure-
coefficients recommended by the Commissions for ments of H'(O.07) and H*(10) will normally provide
the directional dose equivalent, H'(d,fl) are the data adequate information for protection in photon radia-
of Dimbylow and Francis (1989) and those in ICRU tion fields.
Report 47 (see Section 2.6.3).
(193) Values of conversion coefficients for the
Personal dose equivalent
directional dose equivalent at depths of 0.07 and 10
mm in the ICRU sphere, H'(0.07,00) and H'(10,00), (195) A discussion of the quantity personal dose
are given in Tables A.22 and A.23 of Annex 2 [see equivalent is given in Section 2.6.4. At present, no
Paragraphs (189)-(191), 'Ambient dose equivalent,' calculated values for Hp(d) in the human body are
for a discussion of interpolation between the data in available. However, ICRU Report 47 has recom-
Tables]. Variations of the conversion coefficient, mended conversion coefficients for Hp,slab in the ICRU
H'(d,ex)/$, as a function of photon energy and of the slab based on calculations by Grosswendt (1990).
angle, ex, between the radius opposing the incident Data from Till et ai. (1995) and revised data from
field and the principal axis of the ICRU sphere can Grosswendt et ai. (nd) were used in the preparation
be studied through the angular dependence factors, of Tables A.24 and A.25 of Annex 2, which also
R(d,ex), defined by: contain conversion coefficients from air kerma as
well as angular-dependence factors for H p(10,ex) and
R(d, ex) = [H'(d, ex)/$]/[H'(d, 0°)/$] (4.1)
H p(0.07,ex) for angles between 0° and 75°.
and values of R(d,ex) are also included in these tables (196) The personal dose equivalent at depths of
for values of ex from 0° to 180°. These angular 0.07 and 10 mm in tissue slab phantoms has been 33
I E=30 keY I quantities and operational quantities. The protec-
tion quantities given here are the organ absorbed
dose, DT , and the effective dose, E. The operational
quantities provided are ambient dose equivalent,
H*(d), and personal dose equivalent, Hp(d). The
0.216 conversion coefficients given are for irradiation by
0.263
Others monoenergetic neutrons incident in several geom-
etries on the phantoms of interest. The general
methods used to calculate these conversion coeffi-
cients are described in Section 3.
0.072
Colon 4.4.2 Special considerations for neutrons
(198) Conversion coefficients given in this report
0.139 are for irradiation by incident monoenergetic neu-
Stomach trons. In practice, exposure to monoenergetic neu-
trons rarely occurs. The energy of neutrons in radia-

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0.109 0.115 tion fields usually extends over a wide range-in
Thyroid Breast some instances by as much as 10 orders of magni-
tude in energy. Furthermore, most so-called 'neutron
fields' are mixed radiation fields, almost always
associated with photons and sometimes other radia-
tions. If the conversion coefficients for such fields are
to be evaluated, appropriate averaging of coefficients
I E=200 keY I for monoenergetic particles over the relevant spectra
must be carried out (see Section 4.2.1).
(199) Within a body, neutrons undergo many inter-
actions by which they lose energy until they are
0.139 finally absorbed in or escape from the body. Many
different types of secondary particle may be pro-
0.325 duced during this slowing-down process. The ener-
gies (and consequently the LETs) ofthese secondary
0.128 particles are distributed over a wide range. The
Testes distribution of absorbed dose in terms of LET (and
therefore quality factor) at a given position in the
phantom is determined by many variables of which
the most important are the interaction cross sec-
tions, secondary-particle energy spectra, and trans-
0.121 port of the secondary particles from the point of
0.08 Colon interaction to that position. Thus, the deposition of
Red bone energy at any point in a body resulting from external
0.094 0.113
marrow irradiation by neutrons is a complex process and is
Ovaries Lung strongly energy-dependent.
Fig. 16. Relative contributions of specific organs to effective (200) The production of secondary photons by
dose, E, for photons with 30 and 200 keV energy inAP irradiation
neutron interactions is of particular importance
geometry on an adult anthropomorphic computational model.
because of the considerable penetration of these
photons in tissue. In particular, the 2.2 MeV photons
chosen because operational quantities at these two that are emitted during capture ofthermalised neu-
depths are used for monitoring weakly and strongly trons in hydrogen via the 1H(n;y )2D reaction playa
penetrating radiation. Angular dependence factors significant role in the deposition of energy in the
are given for <X values up to 75°. human body and are, as a result of Compton scatter-
ing, the source of secondary photons of above about 1
MeV in energy in a body irradiated by neutrons. For
4.4 Conversion Coefficients for Neutrons
neutrons of incident energy up to about 1 MeV,
secondary photons deposit the major fraction of the
4.4.1. Introduction
absorbed dose deep in the body. At a depth of 10 mm
(197) This section provides reference conversion in the body, photons contribute 90% of the absorbed
34 coefficients from neutron fluence to both protection dose from irradiation by thermal- and intermediate-
energy neutrons; at neutron energies above 10 keV MORSE-CG and SAM-CE. In addition, special codes
the contribution to absorbed dose from photons falls developed and operated at JAERI (Yamaguchi, 1993)
sharply and is less than 20% at 1 MeV (Dietze and and PTB (Hollnagel, 1990) were used.
Siebert, 1994). (205) The MCNP code was used by six groups of
(201) As the incident energy of the neutrons in- authors. When coupled with the ENDFIB neutron
creases, other radiations play an increasingly impor- cross-section data files, this transport code was
tant part in the deposition of energy. At the incident limited to calculations for neutron energies below 20
neutron energies considered in this report, protons MeV. However, by extending the cross-section data
are, after photons, the next most important source of files, Leuthold and Schrauber (1992) were able to
absorbed dose in human tissue. At thermal neutron perform calculations for energies up to 30 MeV with
energies, the reaction 14N(n,p)14C (which produces the MCNP code. The codes MORSE, SAM-CE, and
protons of about 600 keV) contributes the greater the customised codes of Hollnagel were also limited
part of the absorbed dose from protons. At energies to 20 MeV by the cross-section data (see Table 5).
above about 1 keV, the energy deposited by recoil (206) Nabelssi and Hertel (1993a,b, 1994) used the
protons from elastic scattering on hydrogen becomes LAHET code for neutron energies up to 180 MeV.
important, while at energies above a few MeV the This code can be applied to calculations of the

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production of charged particles by nuclear reactions transport of high-energy particles. For calculations
[(n,D), (n,T), (n,a), etc.] increasingly becomes an
up to incident neutron energies of 5 GeV in the ICRU
important mechanism for the deposition of energy.
sphere, Sannikov and Savitskaya (1993, nd) used the
(202) At neutron energies below 20 MeV, the
HADRON code.
absorbed dose is calculated by means of the kerma
(207) The kerma approximation was used by all
approximation, but at higher energies, secondary
authors for energies below 20 MeV (Le., charged
charged-particle equilibrium is not always achieved
particles were not transported from the interaction
and the transport of secondary charged particles
must be considered (the range of20 MeV protons in point) (see Section 3.4.1, for a discussion of the
tissue is about 4 mm). The kerma approximation and kerma approximation). Of the transport codes listed
its limitations are discussed in detail in Section in Tables 5 and 6, only LAHET and HADRON treat
3.4.2. the transport of energetic charged particles away
(203) The definition of the protection quantities in from the point of interaction. In their calculations,
ICRP Publication 60 recommended significant Nabelssi and Hertel (1993a, 1994) and Sannikov and
changes with respect to radiation quality weighting. Savitskaya (1993, nd) transported charged particles
In calculations of these quantities, the use of a down to 20 MeV and then used the kerma approxima-
quality factor related to LET [the Q(L) - L relation- tion.
ship] was replaced by the radiation weighting factor, (208) Special considerations apply to the calcula-
WR, which is determined only by the radiation inci- tion of energy deposition by thermal neutrons. Ther-
dent on the body (Le., not by the radiation at the mal neutron-scattering is strongly dependent on the
point of interest) but is applied to the mean absorbed molecular binding of hydrogen (e.g., water or polycar-
dose in the relevant tissue. Use of the Q(L) - L bonate) and the chemical composition ofthe material
relationship was, except in some exceptional circum- in which the scattering takes place. Furthermore, in
stances when it may be used in the calculation of the thermal region, the energy distribution of neu-
protection quantities, reserved for calculation of the trons is important because both the tissue kerma
operational quantities (see Section 2.4.2 for further coefficient and the IH(n;y)2D and 14N(n,p)14C reac-
discussion). tion cross sections vary inversely with neutron veloc-
ity. The value of the calculated mean kerma coeffi-
4.4.3. Methods of calculation cient for thermal neutrons and the secondary photon
fluence therefore depend on hydrogen-binding and
the precision with which the thermal energy distribu-
Computer codes tion is described (i.e., on the number and width ofthe
(204) General features of the transport codes used energy groups selected in the low-energy range).
for photon calculations are discussed in Section (209) The number of energy groups (often referred
3.4.2. Several different codes were used to calculate to colloquially as energy-bins) used by the various
the data reported here. The Joint Task Group evalu- groups of authors differed widely. For example,
ated data from nine groups of authors. The computer Yamaguchi (1993) used only one thermal energy
codes used by each group in the calculation of group while Leuthold et ai. (1992) used 20 energy
protection and operational quantities are listed in groups for neutrons below 1 eV. A summary is given
Tables 5 and 6, with brief descriptions of the codes in Tables 5 and 6. The choice of number and width of
given in Section 3.4.2. Several so-called 'standard' energy groups significantly influences the values of
Monte Carlo codes were used: LAHET; MCNP; the conversion coefficients calculated by the various 35
groups of authors (Schuhmacher et al., 1994). The very few experimental cross-section data were avail-
differences between the calculations are greatest for able in the physical databases and the needed cross
deep-lying organs and at neutron energies below 1 sections used were derived from theoretical calcula-
ke V when the neutron degradation process and the tions by applying intranuclear cascade and evapora-
contribution of secondary photons are most impor- tion models.
tant (see Section 4.4.4). (214) Two recent changes in the Commissions'
recommendations (discussed in Section 4.4.2) influ-
ence the values of the operational quantities. In the
Models and phantoms first place, a new Q(L)-L relationship was intro-
(210) Most of the calculations of protection quanti- duced in ICRP Publication 60. Secondly, the applica-
ties reviewed were made with adult models. Limited tion of the new stopping-power data published in
data were available for children. Calculations were ICRU Report 49 (ICRU, 1993a) for protons and alpha
performed for the adult phantom using either a particles in liquid water results in a decrease in Q for
hermaphrodite MIRD-5 phantom or modified MIRD- neutrons of up to 25%, depending on neutron energy.
based phantoms (ADAM and EVA) with sex-specific These two effects are in opposition but their net
differences (Kramer et al., 1982). The operational influence is an increase in the value ofQ for neutrons
quantities were calculated in the models specified for of up to 40%.

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the operational quantities, the ICRU sphere and (215) For two reasons, the increase in the mean
slab phantoms, both of which are made of ICRU- quality factors, which should be applied to the
tissue substitute. Tables 5 and 6 summarise the absorbed dose in phantoms, is much smaller than
models used by the various groups. the extreme increases in the values Qn(E) indicated
(211) Most of the authors used sex-specific phan- for monoenergetic neutrons. The absorbed dose in
toms based on the ADAM and EVA models in their the body results from the sum of the three contribu-
calculations. Some made calculations for a number tions from unscattered neutrons, scattered neutrons
of organs and tissues different from those specified in and secondary photons. Firstly, the secondary pho-
ICRP Publication 60 and in the Kramer-Drexler tons have a mean quality factor, Q, which is taken to
equation [eqn (2.13)] (Kramer and Drexler, 1982). be 1 and, because photons make a significant contri-
The number of organs included ranged from 20 bution to the absorbed dose, the mean quality factor
(Leuthold et al., nd) to as many as 60 (Yamaguchi, for the mixed radiation will be correspondingly re-
1993). Two groups used hermaphrodite phantoms duced. Secondly, the mean quality factor for the
that included both male and female organs and neutrons, Qn, must be calculated by averaging over
tissues [the MIRD-5 phantom (Snyder et al., 1978) the corresponding neutron spectrum. The net in-
and Cristy's adult model (Cristy, 1980)]. A discussion crease in Qn will be smaller than the extreme
of the evolution and development of these models increases in Qn. Both effects result in a smaller
and phantoms to accommodate the prescriptions of overall increase in the mean quality factors inside a
the ICRP may be found in Section 3.3.3. body than might at first sight be expected from the
(212) Calculations were made in phantoms of increases in the values ofQn(E) indicated for monoen-
different size, representing different ages, based on ergetic neutrons.
Cristy's models (Yamaguchi, 1994d).
4.4.4 Available data
Physical data
(213) Several different databases containing physi-
Protection quantities
cal data were used by the various groups of authors.
The principal sources of neutron cross sections were (216) The Joint Task Group reviewed organ dose
the already available data files: ENDFIB-IV (NNCSC, data from the calculations of seven groups of authors
1974); ENDFIB-V (Garber, 1979) and JENDL-3 (Shi- (see Table 5). These authors provided data sets of
bata et al., 1990). Neutron kerma coefficients were conversion coefficients for organ absorbed doses and
either calculated directly from cross-section data effective doses under various whole-body irradiation
(Morstin et al., 1992) or taken from the tables of geometries. The data were available for the irradia-
values published in ICRU Report 26 (lCRU, 1977), tion geometries: antero-posterior (AP); postero-
from Caswell et al. (1980), or from White et al. anterior (PA); left and right lateral (LLAT and
(1992). These neutron cross-section databases were RLAT) [simply lateral (LAT) if the organ is posi-
generally in good agreement for neutron energies tioned symmetrically with respect to the vertical
below about 10 MeV but some differences in the data axis of the body]; rotational (ROT); and isotropic
for cross sections and kerma coefficients became (ISO) (see Section 3.5). All available organ-dose data
evident at higher energies. For calculations at neu- were considered for this report and, with very few
36 tron energies above 30 MeV using the LAHET code, exceptions, included in the final evaluation of the
reference conversion coefficients (see Section 4.4.5). between, the various data sets. The statistical uncer-
Figure 17 shows organ absorbed doses for a few tainties in the calculated conversion coefficients for
selected organs as a function of neutron energy. The the organ absorbed doses were estimated by their
curves show absorbed dose per unit fiuence, DT/c!J in authors to be typically much less than 10%. How-
units of pGy cm2 , for the colon, female breast, lung, ever, comparisons of organ absorbed dose data pro-
red bone marrow, testes and skin of an anthropomor- duced by separate groups revealed that the scatter of
phic model irradiated in AP geometry. A complete set the data between the different authors is, in some
of evaluated organ absorbed dose and effective dose cases, much higher than the estimated statistical
data are presented graphically in Annex 1 and uncertainty. In the worst cases, this scatter is more
tabulated in Annex 2. than a factor of 2 although, in most cases, it is much
(217) With only a predictable few exceptions, there lower. This suggests the possibility of some undiscov-
are no significant differences between the organ-dose ered sources of systematic uncertainty in the data.
data obtained from calculations with the hermaphro- (220) Figures 18 and 19 show two selected ex-
dite model compared to those with the male or amples ofthe variability ofthe calculated organ-dose
female model. The exceptions are for the breast and data. Individual data points calculated by different
the gonads (for all irradiation geometries) and for authors are plotted as a function of neutron energy,

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the lungs under the AP irradiation (shielding by the with the solid line indicating evaluated conversion
female breast). coefficients. Figure 18 gives an example for the
female liver of the satisfactory agreements between
the data of different authors. Figure 19 gives an
Operational quantities
example for the male colon where there are greater
(218) Conversion coefficients for the operational variations in the data of different authors. A set of
quantity ambient dose equivalent, H*(10), have been figures demonstrating the variability of the organ-
calculated by five groups. In addition, two of the dose data is given in Figs. A.36-A.55 in Annex 1.
groups performed calculations for H'(10,a) and Data are shown for organs near the surface of the
H p ,slab(10) using a slab phantom (see Table 6). Values body (testes, Fig. A.43); for organs near the midline
of the ambient dose equivalent, H*(10), and personal ofthe body (ovaries, Fig. A.42; lungs, Fig. A.49); for a
dose equivalent, H p ,slab(10,a), as evaluated by the case where individual data sets are in good agree-
Joint Task Group are presented graphically as a ment (liver, Figs. A.44-A.48); and for a case where
function of neutron energy in Annex 1 and tabulated individual data sets scatter is more pronounced
in Annex 2. (stomach, Figs. A.51-A.54). Figure A.50 shows an
example for calculations of the remainder absorbed
dose.
Analysis of the variability of the data:
(221) A detailed and rigorous analysis of possible
protection quantities-organ absorbed dose
systematic errors leading to an explanation for this
(219) The organ-dose data sets from seven groups scattering of organ-dose data is difficult and beyond
of authors (Table 5) permit some conclusions to be the scope of this report. It is possible, however, to
drawn on the scatter both within each of, and offer some qualitative explanations: the variations

102 breast
lungs
colon
red bone marrow
testes
skin

10·1~~~~~~~~~~~~~~~~~~~~~~~
10.9 10-3 10.7 10-6 10.5 10-4 10.3 10.2 10.1 100 101 ]02
Neutron energy (MeV)
Fig. 17. Organ absorbed dose conversion coefficients for selected organs in AP irradiation geometry, as a function of neutron energy, for
an anthropomorphic computational model. 37
1()l - - - Evaluation
GSF-I
M
..-. " GSF-2
University of Texas
S
Col
o JAERI
AGH&KFA
» 10'

-
c"
Co

10-' 10-· 10-' 10-6 10-5 to" 10-3 10-2 10-' 10' 10' t()l
Neutron energy (MeV)
Fig. 18. Variability between Institutes of organ absorbed dose conversion coefficients exemplified by dose to the female liver as a

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


function of energy for neutrons incident upon an anthropomorphic model in RLAT irradiation geometry_ The solid line shows the evaluated
best fit to the data_

between individual data points of the many data sets Protection quantities-effective dose
may arise from differences in the various anthropo-
(223) The quantity effective dose is robust against
morphic models, transport codes and physical data-
changes in individual organ doses. Thus, for some
bases used by the authors.
(222) Modelling of the many organs and tissues in specific organs there are quite large differences
the body differs in the various codes. At neutron between the calculated organ doses from various
energies above 1 MeV, the organ absorbed doses authors, but there is nevertheless good agreement in
generally agree to within 30%. Differences between the values of the quantity effective dose calculated.
individual data points are most pronounced at neu- Figure 20 shows one particular example of the
tron energies below 100 keY and for the deeper comparison of estimates of E obtained by different
organs (e.g., stomach and colon) in which secondary authors. A complete set of such comparisons for
photons contribute a significant fraction of the total irradiation in AP, PA, RLAT, LLAT, ROT and ISO
absorbed dose (see Figs. A.37-A.41 and A.51-A.54). geometries is given in Figs. A. 56-A. 61 of Annex 1.
The large differences between the data for the oe- These figures for E may be compared with the set of
sophagus are probably due to different modelling of similar comparisons for individual organ absorbed
the organ, which was not included in the original dose data, also in Annex 1, where graphs for the bone
MIRD phantom. marrow, colon, liver, lungs, ovaries, remainder, stom-

- - - Evaluation
o
GSF-I
" GSF-2
M
..-. o University of Texas
10' o JAERI
S
Col
AGH&KFA
>.
PNL
<Xl
Ol
Ol
......
r:--
-
c"
C.

I§;' 10'
000
000
v
o 0 0
v

~
to 0
~

~
0
~
Q) -- "
0 ,,0

~
10-'

-
C,.) S~~-L~~~~~L.~~~~~~-L~-L~~~~
10-' 10-· HI" lit' 10-5 10"
Neutron energy (MeV)
10-3 10.2 10-' 10' 10' t()l

Fig. 19. Variability between Institutes of organ absorbed dose conversion coefficients exemplified by dose to the male colon as a function
of energy for neutrons incident upon an anthropomorphic model in RLAT irradiation geometry. The solid line shows the evaluated best fit to
38 the data.
10' ...,rn
I':
Q)
- - - Evaluation '8
v GSF-I is
Q)
GSF-2 0

M
- ey 10'
D
0
UniAustin
JAERI
AGH&KFA
PNL
Co.)
I':
0
'Cil
....Q)
>
> • PTB I':

-
0
~ Co.)
c.

~ 10' • 0 • o·

-
til

10·~~~~-L~~~~~~~~~~~~~~~~~LU

1~ 1~ I~ 1~ 1~ I~ 1~ 1~ 1~ 1~ 1~ 1~
Neutron energy (MeV)

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


Fig. 20. Variability between Institutes of effective dose conversion coefficients as a function of energy for neutrons incident in AP
irradiation geometry on a human adult anthropomorphic computational model. The solid line shows the evaluated best fit to the data.

ach, testes, thyroid (Figs. A.36-A.55) are given for a symbols) and the best fit evaluated by the Joint Task
variety of irradiation geometries of sex-specific adult Group (shown by a solid line). The variations be-
anthropomorphic computational models. As may tween the individual data points may be more easily
readily be seen, the corresponding variability of the seen in Fig. 21 where the ratios of original data for
data sets for the effective dose from the various H *( lO)!CPto the best-fit value is given as a function of
authors is much smaller than that for some of the neutron energy. The variations between the data
individual organ doses. points are generally less than ±10%.

Operational quantities 4.4.5. Conversion coefficients and analysis:


protection quantities
(224) Variations between the data for the opera-
tional quantities from these groups are lower than
Organ and tissue doses
those for the organ absorbed doses. As an example,
Figs. 21 and 31 compare data calculated by several (225) The organ absorbed dose data sets for 13
groups for the fluence to ambient dose equivalent organs and tissues (including the 'remainder') and
conversion coefficient, H*(10)ICP. Figure 31 shows the six irradiation geometries for the seven authors were
individual calculations by five groups (identified by assessed (see the summary in Table 5). All these

.••... _.... 1.0


GSF
o IHEP
v PTS-!
PTS-2 v
o University of Texas •
......

~:s
-<
.-.. I

o .....
....."

*
::t:
0.7S ......:'""'""""'""":......"'-7~"-:-.......'-:'-'......"7'".......~~:'""'""""'""":........"'-::'-~"-:-'-.......'-::'"'
10-9 10~ 10-7 10"' 10.5 10-4 10-3 10-2 10'\ 10° 10· 102
Neutron energy (MeV)
Fig. 21. Variability between Institutes of ambient dose equivalent conversion coefficients, H *(10 )l<P. The ratio of original data for the
conversion coefficients provided by various authors, to the best fit evaluated by the Joint Task Group, is given as a function of neutron
energy. 39
available data (a total of about 900 data sets) were able differences between the two lateral conversion
considered for this report and, with few exceptions, coefficients.
included in the analysis. Details of the selection (229) Table A.37 gives conversion coefficients for
criteria for inclusion ofthe data for analysis and the the remainder. These values were evaluated from
evaluation procedure have been described by Siebert the remainder data given by the various authors,
and co-workers (nd). In a few instances, it was and are based on data for those separate organs and
necessary to exclude the data for a single organ from tissues that make up the remainder (adrenals, brain,
one group of authors. In one case, for example, the kidney, muscle, pancreas, small intestine, spleen,
oesophagus was not actually modelled in the code upper large intestine, thymus, and uterus). All au-
but a surrogate organ used (Stewart et al., 1993). As thors calculated their remainder data by averaging
another example, the thermal neutron data (Yamagu- the organ and tissue doses with equal weighting:
chi, 1993) were also excluded because in the Yamagu- mass-averaging and the specific rule known as 'foot-
chi code a single neutron group in the thermal region note 3' were not applied (for further discussion see
was used and chemical binding of hydrogen was not Section 2.5.4).
taken into account. This resulted in much higher (230) Data are given for neutron energies from
doses than those obtained by all the other authors thermal up to 180 MeV. If precise data are needed at
(see Section 4.4.3). In a few other cases, data for one energies other than those listed in the tables, it is

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


particular organ and/or a single irradiation geom- recommended that interpolation be carried out using
etry were excluded because the data deviated strongly a 4-point (cubic) Lagrangian interpolation formula
from all other data sets. on a log-log scale.
(226) As a basis for the reference conversion
coefficients, a set of 'best estimates' ofthe conversion Effective dose
coefficients for absorbed dose per unit fiuence was
derived for each of those organs for which weighting (231) The effective dose data were determined
factors were given in ICRP Publication 60 (ICRP, from evaluated organ absorbed dose data. The conver-
1991a). In most cases, the organ doses were calcu- sion coefficients for the organ equivalent doses,
lated in sex-specific models and values of organ dose HT/iJJ, were obtained by multiplying D~iJJ by the
for the two sexes were averaged. In the data analy- corresponding radiation-weighting factor for neu-
sis, the average values of organ doses calculated in trons of the incident neutron energy.20 Table A.41
sex-specific modes were combined with those calcu- summarises the recommended conversion coeffi-
lated in unisex phantoms. cients for the effective dose per unit fiuence for
(227) The data points from each group of authors whole-body irradiation by neutrons from thermal
were combined into one data set for each organ as a energies up to 180 MeV in the AP, PA, LAT, ROT, and
function of neutron energy, resulting in one com- ISO irradiation geometries. Ifprecise data are needed
bined data set for each organ and for each gender. at energies other than those listed in Table A.41, it is
Every point in a given data set was given the same recommended that interpolation be carried out using
weight in the analysis. A least-squares spline fit was a 4-point (cubic) Lagrangian interpolation formula
used to derive the organ absorbed dose as a single- on a log-log scale.
valued, smooth function of incident neutron energy. (232) Figure 22 shows the values of the conversion
This function was then used to evaluate data at coefficients plotted as a function of neutron energy
specified neutron energies. The evaluated functions for the various irradiation geometries.
for each organ are shown as a function of neutron
energy in Figs. A.20-A.34 of Annex 1. For most Energy dependence of effective dose
organs, the data averaged over both sexes are given.
Data for the sex-specific organs, female breast and (233) The dependence ofthe organ dose conversion
ovaries, and the testes, are also provided. factors upon neutron energy is determined, to some
(228) Tables A.26-A.40 present the evaluated con- degree, by the depth of the organ in the body but
version coefficients for those specific organs [i.e., the there are general similarities in the trends for all
bladder; bone (red-marrow); bone (surface); breast; organs. An increase in the conversion coefficients is
colon; gonads (ovaries, testes, and the average value); observed from thermal energies to about 1 eV; from 1
liver; lungs; oesophagus; remainder; skin; stomach; eV to about 10 keV, the coefficients are almost
and thyroid] for which the ICRP recommends tissue- independent of energy. At energies between 10 keY
or organ-weighting factors. For most organs, only and about 1 MeV a sharp increase in the coefficients
one data set for the LAT irradiation geometry is may be seen. The onset of this increase depends on
given. For those organs that are asymmetrically the depth of the organ in the body; in broad terms,
located in the trunk (e.g., colon, liver and stomach),
separate data are given for the LLAT and RLAT 20 The expression 'tissue or organ' is often abbreviated to 'organ'
40 irradiation geometries because there are consider- in this section.
..,"'
a
Q)
AP 'u
PA !:EQ)
R-LAT o
L·LAT Co)
ROT §
ISO '0;
....Q)
>
§
Co)

1~~~-L~~~~~~~~~~~~~~~~~~~
1~ 1~ 1~ 1~ 1~ 1~ 1~ I~ 1~ 1~ 1~ 1~
Neutron energy (MeV)

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Fig. 22. Reference conversion coefficients for effective dose as a function of energy for neutrons incident in various irradiation
geometries on adult anthropomorphic computational models and averaged for both sexes. These reference data are also given in TableA.4l.

the deeper the organ the higher the energy of the LAT, ROT, and ISO irradiation geometries, but for AP
onset (see Fig. 17). In the energy range 10 keV to 1 irradiation geometry the effective dose actually shows a
MeV, proton recoils and other charged secondary small decrease (see Figs. A.56-A.61 inAnnex 1).
particles from neutron interactions begin to make a (235) As an example of this effect, Fig. 23 shows the
significant contribution to the absorbed dose. At absorbed dose in the testes (a shallow, frontally located
incident energies greater than 10 MeV, the absorbed organ) as a function of energy in both AP and PA
dose at locations near the irradiated surface of the geometries. In AP geometry, it may be seen that for
body decreases because energy is transported from neutron energies above about 1 MeV, the absorbed dose
the point of interaction by charged secondary par- in the testes, and therefore the significance in its contri-
ticles whose ionisation ranges increase with energy. bution to effective dose, decreases. At energies below 10
(234) Because several organs of importance in MeV, in the other geometries (LAT, ROT, ISO), the
determining the value of the effective dose (i.e., those contribution of the absorbed dose to the testes is of less
organs with the larger tissue weighting factors) are significance to E (see Fig. 23 and Figs. 25-29).
located near the front of the body, the energy depen-
dence of the effective dose for AP irradiation geom-
Angular dependence of effective dose
etry at high energies is different from that of other
irradiation geometries. Above 10 MeV, the effective dose (236) The angular dependence of conversion coeffi-
continues to increase with neutron energy for the PA, cients for the effective dose is complex because it is

Testes (AP) ..-r.I'...


Testes (PA)
Ovaries (AP)
Ovaries (PA)

10·1~~-L~~~~~~~~~~'-~~~~~~~~~
10.9 10-8 10" 10-6 10.5 10-4 10.3 10.1 10.1 10° 10 1 101
Neutron energy (MeV)
Fig. 23. Comparison of the absorbed dose in the gonads in AP and PA irradiation geometries as a function of energy for neutrons
incident on an adult anthropomorphic computational model. 41
determined, as is the energy dependence, to some dose. Six figures are presented, one for each of the
degree, by the location of those organs of the human irradiation geometries AP, PA, RLAT, LLAT, ROT,
body with high tissue weighting factors. Neverthe- and ISO. Each of the six figures have two alternative
less, some generalisations are possible: at energies modes of representation of the data. In the first
above 50 MeV, the angular dependence is small (upper) mode, the ratio wTHTIE is plotted as a
because the incident neutrons penetrate deeply into function of neutron energy. Data are shown for those
human tissue. At lower energies, irradiation in AP five organs with the highest weighting factors. In the
geometry always results in the highest effective second (lower) mode, pie charts show the relative
dose, while the LAT irradiation geometry gives the importance of various organs at selected energies.
lowest values. This general observation may be (239) In AP irradiation geometry the gonads are
explained because the inner organs of the body are the largest 'single' contributor to the effective dose
shielded by outer layers of muscle and other tissues (as much as 28% of the value of E at an energy of
ofthe trunk and arms. about 500 keV). In the PA or LAT irradiation geom-
etries, the dominance of the contribution of the
gonads is less pronounced and the relative contribu-
Age dependence of the effective dose
tions of the various organs to the effective dose is-to
(237) Figure 24 shows calculations of effective dose some extent-determined by their location within

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in AP geometry for anthropomorphic computational the body. Figures 25-30 show that, for irradiation in the
models representing children of various ages com- ROT and ISO geometries, the relative contribution of
pared with the adult. At neutron energies below each organ is roughly equal to its corresponding organ-
about 10 keV, the effective dose decreases with weighting factor-almost independently of energy.
decreasing body size, while at higher energies this
trend is reversed. At lower energies, secondary pho-
Conversion coefficients for operational
tons from thermal neutron capture make the largest
quantities: ambient dose equivalent
contribution to the effective dose (the larger the
volume of tissue the more efficient the thermalisa- (240) Conversion coefficients from neutron fluence to
tion process) but at energies above 10 keV, reduction ambient dose equivalent, H*(10), have been reported by
in the absorbed dose in the inner organs (due to Leuthold et al. (1992), Schuhmacher and Siebert (1992),
shielding of the surrounding outer trunk) becomes Sannikov and Savitskaya (1993, nd), Hollnagel (1994b),
increasingly important: the smaller the body the Nabelssi and Hertel (1994), Siebert and Schuhmacher
lower the shielding. As the energy increases above (1994) and Siebert et ai. (nd) (see Table 6). The values
about 10 MeV, the shielding effect of the outer trunk calculated by these authors generally agree to within
is negligible or even reversed. 10% (see Figs. 21 and 31).
(241) Schuhmacher et ai. (1994) have reported a
sensitivity study of the influence of several param-
Relative contribution of specific organs
eters on the numerical values of conversion coeffi-
and tissues to the effective dose
cients and found that the parameters to which the
(238) Figures 25-30 summarise the relative contri- conversion coefficients are most sensitive are the
butions of specific tissues and organs to the effective Q(L) - L relationship selected; the stopping powers

10-9
'"E0 ~

> A l5-YR
(/)
+ 10-YR
Q) 10- 10
00 0
c: v 5-YR
~ Q)
~
..... OJ
r;::
)(

.--
>D Gl ····c····
C. I
1:: Q)
11 )(1
0 <II 10-
~
OJ
0
"C ----------~-{]-- ____ o-____ ~- _____ ~--~,'O
0:: Q)
>
~ U
Ql
;::
8 W
10- 12 2
10- 8 10
Neutron energy (MeV)
Fig. 24. Effective dose as a function of energy and age, for neutrons incident on anthropomorphic computational models, representing
42 children of different size (corresponding to age) in AP irradiation geometry.
Gonads
0.2 Bone marrow
Colon
- -- --- ........

------- ........ --,,'-~


/;-;;:;;~··,7·
_... _----- __
_---- ------------- ---.. . "
0.1 ... - _-
... ...
.- -
... ... .. ..._ .-"-'- ,
. .><~=~>"'.. . ... / ~. '

Lung
Stomach

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Neutron energy (MeV)

25meV 1 keY
Olhen 33.1"1.

Tesles

TeSles~~~~ ~~
Bone morrow Slomach
Bone marrow
Colon

300 keY 180 MeV


Othen 35.8%

Colon

Fig. 25. Relative contributions of specific organs to effective dose as a function of energy for neutrons incident in AP irradiation
geometry on an adult anthropomorphic computational model (mean of data from ADAM and EVA).

of charged particles; the values ofkerma coefficients (243) Table A.42 summarises the values of the
applied, and the number of energy bins selected in recommended reference conversion coefficients. If
the low-neutron-energy region. precise data are needed at energies other than those
(242) A set of reference conversion coefficients, given in this table, it is recommended that interpola-
H*(10)lcP, as a function of neutron energy in the tion be carried out using a 4-point (cubic) Lagran-
range from thermal to 180 MeV was determined by gian interpolation formula on a log-log scale.
fitting the data from all the authors with no further (244) At energies between 20 and 180 MeV, the
weighting by a least-squares spline fit. Details of the conversion coefficients are based on data from Na-
evaluation procedure are published by Siebert and belssi and Hertel (1994) and Sannikov and
co-workers (nd). The primary data and the spline-fit Savitskaya (1993, nd). These data are consistent
data are shown in Fig. 31. Figure 21 shows a plot of the with other data at energies below 20 MeV but the
ratio of calculated values of H *(lO) to the 'best value' or accuracy of the coefficients at higher energies is
'recommended value' obtained by a spline fit, including subject to the increasing uncertainty of the neutron
variations in the data between the different authors. cross sections with energy. 43
Gonads
Bone marrow
Colon
Lung

0.2
Stomach
....•......••...........~-------- ./'
"/-->' "
/ .: .~\.
.................................. .I '..::\.
_' .. -"'-... - ... - .. - . _" ._' - _. __ . __ ,.f \, "
---------------------- ---------- .... ' ... .."".....-\(",
" --",-" ?' ....,\'
0.1 - -- ------- ' ..... //

I
./ ......... ~

" /

OLL_~~~~L-_u_~ __ ~~~~L_~~~_ _~~

l~ l~ l~ l~ l~ l~ l~ l~ 1~ l~ l~ 1~

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Neutron energy (MeV)

25meV 1 keV

Testes

Bone marrow Stomach Bone marrow

Colon

1 MeV 180 MeV


Olhen 34.0%

Colon Colon
Fig. 26. Relative contributions of specific organs to effective dose as a function of energy for neutrons incident in PA irradiation
geometry on an adult anthropomorphic computational model (mean of data from ADAM and EVA).

Directional dose equivalent cients for directional dose equivalent for neutrons
(245) Values of the directional dose equivalent, are given in this report.
H'(d,D), are of practical utility for area monitoring,
particularly for photon or electron radiation fields
Personal dose equivalent
but are of limited interest in neutron monitoring.
(246) Neutrons of all energies penetrate deeply (247) A discussion of the quantity personal dose
into human tissue and as a practical matter, data for equivalent is given in Section 2.6.4. At the present
H'(0.07,ex) and H'(3,ex) are not needed. In practice, time, data for Hp(d) calculated in the human body
the limitation of E provides adequate protection for are sparse. Hollnagel has reported some preliminary
the lens ofthe eye. Values of H'(lO,OO)fct> are equal to calculations of Hp(lO) at a location in front of the
H*(lO)/4> and values for H'(lO,ex)/4> with ex *- 0° are lung and also explored the use of Hp,testes and
not needed for area monitoring in neutron fields. For Hp,thymus' Until complete calculations have been made,
44 all these reasons, no values of the conversion coeffi· conversion coefficients for Hp,slab are available and
Gonads
Bone marrow
Colon
Lung
Stomach
0.2

... - "'-"'-" '-" '- "'-- "'- "- ' - -


.. ... -....
.',,:-..._ /I
~"" ...... "'~.
/"-.-
0.1 /
,,"{
--------------------------" /// /
_----- , I
....-:;.-:.:: - - - - - - - - - - - ................... J" /

---../

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Neutron energy (MeV)

25meV Othen 43.3% 1 keVOthers 40.9"1.

Stomach ach

Colon

Othen 1 MeV 180 MeV

Testes
-":::'===>1111111

1'!11t~~Iii1ir-Stom.ch
Ovaries Bone marrow ,lomach

Bone marrow
Fig. 27. Relative contributions of specific organs to effective dose as a function of energy for neutrons incident in RLAT irradiation
geometry on an adult anthropomorphic computational model (mean of data from ADAM and EVA).

values of Hp,orgam where the organ is carefully se- (249) Conversion coefficients are calculated for a
lected, may be used as surrogates for Hp,torso (see the range of angles of radiation incidence (a = 0°, 15°,
discussion in Section 5.3.3). 30°,45°,60°, and 75°) on an ICRU slab phantom and
(248) ICRU Report 47 suggests that, for the pur- in the neutron energy range from thermal to 20 MeV
poses of dosemeter calibration under reference condi- (see Fig. 32). These data span the practical range of
tions (e.g., monodirectional neutron beam with fron- angles, where the slab phantom may be used as a
tal incidence), the dose equivalent in a 30 X 30 x 15 reference phantom for the calibration of individual
cm slab ofICRU tissue-equivalent material provides dosemeters. Figure 33 shows the ratio of the per-
an adequate approximation to the backscatter of the sonal dose equivalent in the ICRU slab, Hp,slab (10,a)
human body so that H p (10) may be estimated. Siebert to Hp,slab (10,0°) for the same range of angles.
and Schuhmacher (1994) have reported values of (250) It has been suggested that the ICRU sphere
H p ,slab(10,a)lcP that are summarised in Table A.42 in be used as a phantom for use in calibration of
Annex 2 and shown in Fig. 32. individual dosemeters (ICRU, 1985). Although accept- 45
Gonads
Bone marrow
Colon
Lung
Stomach
0.2

......... ...
..... .......
.-' - ,.- . _ ., - -' - -"'-' ::';:.~.::.:.:~-=-..
' .....
0.1
--=-~--=--;=- ----- --=.--...=- =.:--=--=-=

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Neutron energy (MeV)

25meV

Stomach

Lung

1 MeV Othen 39.0% 20 MeV

Stomach

Fig. 28. Relative contributions of specific organs to effective dose as a function of energy for neutrons incident in LLAT irradiation
geometry on an adult anthropomorphic computational model (mean of data from ADAM and EVA).

able in principle, the ICRU phantoms with a flat sorbed doses in a few selected organs, and for
front surface are of greater practical utility. In this effective dose (Schultz and Zoetelief, 1996, nd). For
report, no data for H'(lO,a)ICP with the ICRU sphere the operational quantities, the discussion is focused
are given for neutrons. on providing reference values of conversion coeffi-
cients for the directional dose equivalent, H'(d,a),
4.5. Conversion Coefficients for Electrons which, in the case of irradiation by electrons of
energy in the range considered here, is also an
4.5.1. Introduction adequate numerical approximation to the personal
(251) This section principally discusses conversion dose equivalent, Hp(d).
coefficients linking fluence to the operational quanti-
4.5.2. Special considerations for electrons
ties because data for organ absorbed doses are
sparse for electrons. Some limited data for the (252) Irradiation of the skin, the lens of the eye,
46 conversion coefficients are available for organ ab- and other superficial organs is of principal concern in
Gonads
Bone marrow
Colon
Lung
Stomach
0.2

0.1

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Neutron energy (MeV)

25meV 1 keY
31.6% Othen 31.2%

Stomach Stomach

1 MeV 180 MeV


Othen 36.80;.

Stomach

Colon Colon

Fig. 29. Relative contributions of specific organs to effective dose as a function of energy for neutrons incident in ROT irradiation
geometry on an adult anthropomorphic computational model (mean of data from ADAM and EVA).

radiological protection for electron energies below 10 4.5.3. Methods of calculation


MeV because the electron range is small. The range
of electrons in tissue increases from about 50 p,m at
Computer codes
60 keY to about 50 mm at 10 MeV. There is therefore
a need to determine the absorbed dose in volumes (253) Several different codes were used to calcu-
having very small thicknesses and located at shallow late the data reported here and brief descriptions of
depths in the body. Suitable models must be con- these codes are given in Section 3.4.2. For calcula-
structed (see Section 4.5.3). Simplified models (phan- tion of the protection quantities, Schultz and Zoete-
toms) of the body, such as the slab or the ICRU lief (1996, nd) used the MCNP-4 code to determine
sphere, are satisfactorily representative of the irra- organ absorbed doses. The MCNP-4 code was also
diation conditions involved in radiological protec- used by Padoani (1993) for calculation of the opera-
tion. tional quantities. Operational quantities were also 47
Gonads
Bone marrow
Colon
Lung
Stomach
0.2

0.1

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Neutron energy (MeV)

25meV 1 keY
Ollt.n 32.5%

Stomach Stomach

CoJon Colon Lmg

1 MeV 20 MeV
Olh.n 35.4% Oth.n 33.0%

Testes
~~~

Bone marrow

Colon Colon

Fig. 30. Relative contributions of specific organs to effective dose as a function of energy for neutrons incident in ISO irradiation
geometry on an adult anthropomorphic computational model (mean of data from ADAM and EVA).

calculated by Hirayama (1994), Petoussi et al. (1993) , (255) For the calculation of dose to the skin, the
Petoussi-Henss et al. (1994), Ferrari and Pellicioni above authors used a model of the skin, which
(1994b) and Ma (1995) using the EGS4 code; by consisted of three layers: a surface layer (0.07 mm
Gualdrini et al. (1994) using the MCNP-BO code thick), which is insensitive to radiation; a second
(Guaraldi and Padoani, 1994a,b) and by Grosswendt sensitive layer 1.93 mm thick and, finally, a third 20
(1993, 1994a) using the PTB-BG code. mm thick layer of tissue.
(256) Schultz and Zoetelief (1996) also calculated
the dose to the lens of the eye by considering an
Models and phantoms
electron beam, of radius 80 mm, impinging on the
(254) Calculations of conversion coefficients for face of a MIRD phantom. By concentrating the
organ absorbed doses and effective dose were made electron tracks to the small volume ofthe lens of the
using the male and female MIRD phantoms (Schultz eye, the statistical precision of the calculation of
48 and Zoetelief, 1996, nd). absorbed dose was much improved.
- - Cubic Lagrange interpolation

-
GSF
c IHEP
N v PTB-\
E
rrJ
Co
..
CJ 102 o
PTB-2
University of Texas

'-"

Neutron energy (MeV)

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Fig.31. Reference conversion coefficients from several Institutes for ambient dose equivalent for neutrons.

(257) The 'skin dose' is calculated in the sensitive tering was treated using either Moliere multiple-
part (second layer) and this must be considered scattering or Goudsmit-Saunderson multiple-scatter-
when comparing the skin dose with other organ ing theory. Landau energy-loss straggling was used
doses (particularly the lens of the eye) and with the by one group of authors. Table 7 summarises the
appropriate operational quantities. computer codes, physical data bases, anthropomor-
(258) Calculations for the operational quantities phic models, phantoms and irradiation geometries
were generally carried out in slab phantoms consist- used by each group of authors.
ing of ICRU tissue-equivalent material at the three
depths (0.07, 3 and 10 mm) recommended by the
4.5.4. Available data
ICRU. Petoussi et ai. (1993), Petoussi-Henss et ai.
(1994), Grosswendt (1994b) and Ferrari and Pellic- (260) Recent calculations in the MIRD phantoms
cioni (1994b) also made calculations in the ICRU (ADAM and EVA) by Schultz and Zoetelief(1996, nd)
sphere. have given data for the organ absorbed dose, HE and
E, for irradiation inAP geometry. A complete evalua-
tion of calculated values of the dose equivalent to
Physical data
fluence ratios, H'(d,ex)/iP or Hp(d,ex)/iP, for electrons
(259) Databases and general theories of sampling in the energy range of 50 keV to 10 MeV is presented
the particle histories in electron and photon trans- in PTB Report DOS-24 (Grosswendt and Chartier,
port are described in Section 3.4.2 (see also ICRU, 1994; see also Chartier et ai., 1996). This report uses
1996). Most of the authors depended upon condensed basic data published by Grosswendt (1993, 1994a)
history models for their calculations. Multiple scat- and Hirayama (1994), and includes contributions
from Ma (1995), Gualdrini et ai. (1994), and Padoani
(1993).

--0"
.............. IS· 4.5.5. Conversion coefficients and analysis:
-------. 30" protection quantities
45·
60"
_._._._. 7S·
Organ and tissue doses
(261) There are few organ absorbed dose data for
irradiation by electrons published in the scientific
literature. ICRU Report 43 gives dose distributions
in complex anthropomorphic phantoms resulting
from irradiation by electrons of energy between 5
Neutron energy (MeV) and 46 MeV, calculated using a simulation code
Fig. 32. Conversion coefficients for Hp,slab(IO,a) as a function designed for radiotherapy treatment planning (ICRU,
of energy and angle ofincidence for neutrons incident on the ICRU 1988). Schultz and Zoetelief (1996, nd) have calcu-
slab as a reference computational model. lated organ dose and effective dose data using the 49

- ,~.--- ..... --.. -----..-.. - .'..../ .../~:; ~?- / ."


~.-'

o 15· ,-/-- / / //
~ 0.8
-----------------------,,-/ .. / / /
....
~
30°
_ ._ .. _ .. _ _ _ / .../
.. /
/ i
I

::t:: / ./ '- ._ .. - _.. / i


!
-....o....
0.6
_ ... _ .. / I
~ 45° i
-- I

-
::r::""
0.4

0.2
60°
.- -"- -'- '- '- ,/
/
/
i
i

_/
75°
o~~~~~~~~~~~~~~~~~~~~~-U

1~ 1~ l~ 1~ 1~ 1~ 1~ 1~ 1~ l~ l~
Neutron energy (MeV)

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Fig. 33. Angular dependence of the conversion coefficients for Hp,slab shown by the ratio Hp,slab( lO,a) to Hp,slab(lO,OO) calculated in the
ICRU slab. The legend for the various curves is similar to that in Fig. 32.

MCNP-4 code in the adult male and female MIRD- Operational quantities: ambient
type phantoms (ADAM and EVA) irradiated by dose equivalent
monoenergetic electrons in the energy range of 100
keV to 10 MeV, and in AP geometry. Conversion (266) For electrons with energy between 70 keV
coefficients for a few organs are given in Table A.43 and 10 MeV, the greater part of the energy range
in Annex 2. covered in this report, the ambient dose equivalent is
oflittle interest. Ifrequired, values of H*(10) may be
obtained from the calculated values of H'(10,OO)
Protection quantities: effective dose because these two quantities have the same numeri-
(262) Schultz and Zoetelief (1996, nd) have esti- cal values at higher energies (see Section 4.3.5).
mated effective dose data from their organ absorbed
dose data, calculated for the conditions just de- Directional dose equivalent
scribed; these data are also presented in Table A.43.
(267) The operational quantity of greatest interest
for electron irradiation is the directional dose equiva-
Energy dependence of effective dose lent (Section 4.5.2), which is determined in the ICRU
(263) Values of the effective dose plotted as a sphere but, as will be shown, may also be derived
function of electron energy up to 10 MeV are shown from calculations in the ICRU slab.
in Fig. 34. E increases with electron energy as deeper
organs are progressively reached by the radiation. Comparisons of dose equivalent
The skin contributes more than 75% of the effective determinations in the ICRU sphere
dose for electron energies up to about 1 MeV.
and ICRU slab
(268) At electron energies below about 10 MeV, the
Angular and age dependence of the
electron range is much smaller than the radius ofthe
effective dose
ICRU sphere. In addition, the curvature of the
(264) No data are currently available to describe sphere is of negligible influence on the dose equiva-
the variation of the effective dose, in terms of either lent at shallow depths. Thus, the dose-equivalent
angular incidence of radiation or size of the irradi- data calculated in the ICRU sphere and a tissue-
ated body (phantom). equivalent slab are essentially in agreement (Pe-
toussi et ai., 1993; Ferrari and Pellicioni, 1994b;
Grosswendt, 1994b). Therefore, we may write:
Relative contribution of specific organs
and tissues to the effective dose H'(d, a) = Hs1ab(d, a) (4.2)
(265) The organs that most significantly contrib- (269) Values of conversion coefficients from fluence
ute to the effective dose are listed in Table A.43 in to the directional dose equivalent, H'(d,a), are de-
Annex 2. Data for the skin and the lens of the eye are rived from the dose equivalent calculated at depth,
50 plotted in Fig. 34. d, in the 300 mm X 300 mm X 150 mm slab phantom
TABLE 7. - Summary of calculations of the conversion coefficients for protection and operational quantities for electrons ...,rIJ
~
.~
Codes/databases/ Quantities Energy! Energy Angle u
Author model calculated Geometries range points points IEQ)
0
Grosswendt (1993, 1994a) Monte Carlo code: H'(d,ex) Parallel beam 50keVto1OMeV 28 18 c..l
~
PTB-BG d = 0.07,3 and 10 mm .S
Physical data: 00:s ex:s 89° ...
rIJ
Q)
Condensed history model! >
~
CSDA 0
c..l
Moliere multiple scattering
theory
Landau energy-loss
straggling
Model:
ICRU tissue sphere and slab
Gualdrini et al. (1994) Monte Carlo code: H'(d,ex) Parallel beam 50keVto 10 MeV 17 7
MCNP-BO d = 0.07,3 and 10 mm
Physical data: 0° :s ex:s 83°
Condensed history model

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Moliere MS theory
Model:
ICRU tissue slab
Padoani (1993) Monte Carlo code: H'(d,ex) Parallel beam 50keVto 0.8 MeV 9 6
MCNP4-A d = 0.07,3 and 10 mm
Physical data: 0° :s ex:s 75°
Condensed history model!
ETRAN
Goudsmit-Saunderson mul-
tiple scattering theory
Model:
ICRU tissue slab
Petoussi et al. (1993) Monte Carlo code: H'(d,ex) Parallel beam 50 keVto 5 MeV 15 1
EGS4 d = 0.07, 3 and 10 mm
Physical data: ex = 0°
Condensed history model
Moliere MS theory
Model:
ICRU tissue sphere
Ferrari and Pelliccioni Monte Carlo code: H'(d,ex) Parallel beam 70 keVto 10 GeV 34 1
(1994b) FLUKA d = 0.07, 3 and 10 mm
Physical data: nil ex = 0°
Model:
ICRU tissue sphere
Hirayama (1994) Monte Carlo code: H'(d,ex) Parallel beam 50 keV to 10 MeV 13 8
EGS4 d = 0.07,3 and 10 mm
Physical data: 00:s ex:s 89°
Condensed history model
Moliere multiple scattering
theory
Model:
ICRU tissue slab
Schultz and Zoetelief(1996) Monte Carlo code: E, HE, DT for selected organs AP 100keVto 10 MeV 8 1
MCNP-4 ex = 0° Parallel beam
Physical data:
Condensed history model
ITS code (Halbleib et ai.,
00
1992) O"l
O"l
,.....
Model:
MIRD (ADAM and EVA) t-"
to
Skin model 1::0
Eye model 0.
Q)
Ma(1995) Monte Carlo code: H'(d,ex) Parallel beam 50keVto1OMeV 15 7 ~
EGS4 d = 0.07,3 and 10 mm :;J
Physical data: 0° :s ex:s 85% ~
c..l
Condensed history model ......
Moliere multiple scattering
theory
Model:
ICRU tissue slab
51
(271) In most cases, after the consistency between
the different data sets had been verified, the refer-
ence values and associated uncertainties of the
conversion coefficients were obtained by calculating
the mean value of all the different, but consistent,
independent determinations. This simple procedure
could not be used in some cases. For example, it was
modified when the number of separate data points
was limited or when a systematic shift in data over a
specific angular range was observed at neighbouring
a Skin
• Ere ..
o E
n. electron energies. Specific details of the techniques
••••• H. used are described by Grosswendt and Chartier
(1994). In addition, an uncertainty was given for
every evaluated value, making possible an estima-
tion of the fluctuations of single values about the
10°
mean value.
Electron energy (MeV)

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Fig. 34. Protection and operational quantities for electrons.
The effective dose, E , the effective dose equivalent, HE, the organ
absorbed dose, D T , for the lens of the eye and skin, and the
Normal electron incidence
directional dose equivalentH'(d,OO) at depths, d, of 0.07, 3 and 10 (272) Examples of the good agreement between the
mm, as a function of electron energy.
absolute values of the conversion coefficients,
H' (d,OO)!(/), derived from various computer codes
(Grosswendt, 1993; 1994a; Gualdrini et at., 1994;
made of ICRU tissue substitute, under the condi- Hirayama, 1994; Ma, 1995; Padoani, 1993) may be
tions of an expanded radiation field . These conver- seen by inspection of Figs. 35-38.
sion coefficients are tabulated in Table A.44 in (273) Figure 35 summarises data at a depth of 0.07
Annex 2. mm in tissue. The differences between the calculated
data decrease continuously with increasing energy
from about 20% at 70 keY to about 5% at 10 MeV.
Analysis of the variability of the data
(274) The differences between data generated by
(270) Reference values of the fluence-to-dose- different authors is also illustrated in Figs. 36-38
equivalent conversion coefficients were evaluated for but in a somewhat different manner from that in Fig.
normally and obliquely incident electrons. For the 35. These figures plot values of the ratios of H'(d,OO)/(/)
latter, an angular-dependence factor was deter- to the mean value of all the consistent data,
mined as a function of energy and angle ofincidence. H'(d,OO)/(/), at depths of 0.07, 3, and 10 mm in tissue,

+ Grosswendt
11++ 0 Guoldrini
+ 0 Hirayamo
A Ma
3
~
u
1.0
~ .
D

9
Podoani
Petoussi
Ferrari
>
CIl
c:: t
'-' §

.-r:--
'eo +
• I·
CO
-I": +8 +,
m
m
..... 0
0
l • +. II *•* •
r:
lQ

1::
0
d
:.-'

0
A
::r:
~
~ 0.1 0

-
Q
10- 1 10° 10 1
Electron energy (MeV)
Fig. 35. Comparison of data from several authors showing values of H'(0.07,OO) per unit incident electron fiuence, calculated at a depth
52 of 0.07 mm in ICRU tissue substitute.
rn
1.10 r -+0

.~
.:
+ Gro ••wendt

t + 0 Cuoldrin!
Hirayomo
!:EQ)"
~
0 0
...0 110
U
0
0 0 Podoon!
...... 0 + + .:
0
0 0 ... ...0 ... .S
...: +
D 0
Ii + 0
+++ + ...
rn
0 0 2 0
+
Q)

s::0>
ci 0
,..... +++++
r:z:.: 1.00 + ... ... ...
e+'" u
...... 0 0 + ++0 + +
+ 0 0 0 0
q ... ~~o + +
r-
0 DD
ci
,..... 0'"
D 0 0
:z:: ... D

0 D
0
0.90
10- 1 10° 10 1
Electron energy (MeV)

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Fig. 36. Variability of operational quantity data for electrons: the ratio of H '(0.07,OO)IB'(0.07,OO) showing the deviations from the mean
value of estimates by several authors calculated at a depth of 0.07 mm in ICRU tissue substitute.

1.10
+ Gros.wendt
o Guoldrfnl
o Hlroyamo
... 110
......
0
q
,.....
<'\ +0 g ...
I:z:: i ...0
...... 1.00
... g'
0
q 0
~++

0
+ +
+ +
0 +
0
+ u +

,.....
<'1 0
:z::

0.90~--~------~--~--~--~--~--~--~--~
o 5 10
Electron energy (MeV)
Fig. 37. Variability of operational quantity data for electrons: the ratio of H'(3,OO)!B'(3,OO) showing the deviations from the mean value
of estimates by several authors calculated at a depth of 3 mm in ICRU tissue substitute.

1.1 0 r----~--~--~--~--.-----~--~--~--~--"
+ Grosswendt
o Gualdrini
+ o Hirayama
... Ma
......
oo
-
~ + 0
...... 1.00 ~------+--_------------=--------:'--------.-i
+
0 + t A 0
...
OCJ
Ol
q A • ....
Ol
+ + 0 1:-"
8 0
ft
0
...,
lC
...
0
p..
Q)
~
0 ;:J
~
U
0.90 L-~~~ __--,"__--'-__- ' -__ ~ __ ~ __--L-_ _- ' -_ _- ' - ' .....
o 5 10
Electron energy (MeV)
Fig. 38. Variability of operational quantity data for electrons: the ratio of H' (10,OO)IB '( 10,OO) showing the deviations from the mean
value of estimates by several authors calculated at a depth of 10 mm in ICRU tissue substitute. 53
1.10 [)
a
0I~7S·
$
.. [In
0 00
[I

1.00
~ 0

00
go ~ + +
() + +~+ ()
0 0
6- L;. L;. + Grosswendt
,,-... 0 Gualdrini
~ 0.90
r-:
a 1.10 0
[)
0
L;.
Hirayama
Ma
0 01=45" a n Padoani
'-'

-
I~
,,-...
~
f-
1.00

a 0.90
0' - ' 1.10
~ cx~ IS"
+
[)
1.00 o
o

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0.90
10- 2
Electron energy (MeV)
Fig. 39. Values of the ratio R(0.07 ,a)iR (0.07,a) showing the deviations from the mean value of estimates by several authors, calculated
at a depth of 0.07 mm in JCHU tissue substitute, as a function of electron energy and angle a. Data are plotted for values of a = 15°, 45° and 75°.

as a function of electron energy. These figures show Reference coefficients for normal incidence
that deviations from the mean value become smaller
with increasing energy and range from 7 to 3% at a (275) A set of reference conversion coefficients has
depth of 0.07 mm; from 5 to 1% at a depth of 3 mm; been derived at each of the three standard depths
and from 7 to 1 % at a depth of 10 mm if the majority using a procedure that averaged available published
of the data is included. data. This procedure is described in PTB Report

1.10
o

o Ijl
Ijl
0 ... 6
... +
+ + Grosswendt
0 Gualdrini
..- 0 Hirayama
~

-
A Ma
0

-
' -"'
I~

. .-
~
o +
...
+

<Xl
Ol
Ol
.....
-
0
' -"'
~
0.90
1.10
cx= 15°
o

t-=' A
ID
t0
0- o
~
~ 0 .90 ' - - - - ' - - - ' - - - - ' -_ _........_--.l.._ _' - - _ - ' -_ _' - - _ - ' - _ - - - l
8 o 5 10
Electron energy (MeV)
Fig. 40. Values of the ratioR(10,a)IR (10,a) showing the deviations from the mean value of estimates by several authors, calculated at a
54 depth of 10 mm in JCHU tissue substitute, as a function of electron energy and angle a. Data are plotted for values of a = 15°, 45° and 75°.
00

d z 0.07 mm ]
u
....
0 ~o
.....
0 U
1.5
S ~
.S
Q) 00
0 ....Q)
c:
Q) >
"0 ~
c: o
Q)
1.0 U
a.
Q) -O.II1.V
"0 - - 0.2 II.V
.... --0.411.V
e --- 1.0 II.V
:; 0.5 - 4.0 II.V
c>
c: ·····10.01l.V
«

15 30 45 60 75 90
Angle of Incidence (degrees)

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Fig.41. Reference values of the angular-dependence factor for electrons as a function of the angle of radiation incidence at a depth of
0.07 mm in ICRU tissue substitute.

DOS-24 (Grosswendt and Chartier, 1994). The nu- for the three ICRU-recommended depths (0.07, 3
merical values are given in Table A.44 in Annex 2, and 10 mm). Calculations of R(d,o.) were made with
and the corresponding smoothed curves are shown in 0. varying from 0° to 89°.
Fig. 34. The associated standard deviations decrease (277) Good agreement between sets of published
with increasing electron energy. Typical values vary data may be seen from Figs. 39 and 40, which
from 5 to 1.5% at a depth of 0.07 mm and from 3 to compare individual values of the angular-depen-
1.5% at depths of 3 and 10 mm. dence factors (Grosswendt, 1993; 1994a; Ma, 1995;
Gualdrini et al., 1994; Padoani, 1993; Hirayama,
Angular dependence factor 1994) with the mean values, R (d,o.), at depths of
(276) Variations of the conversion coefficient, 0.07 and 10 mm in the ICRU tissue substitute
H'(d,o.)/</), as a function of electron energy and the phantom. The ratios R(d,o.)IR(d, 0.) are plotted as a
angle of incidence, 0., of radiation to the front face of function of electron energy with respect to the angle
the slab can be studied through the angular- of incidence, 0., in these figures. At all depths, and for
dependence factors, R(d,o.), defined by: the preponderance of the data, deviations from the
R(d, 0.) = [H'(d, o.)I</)]/[H'(d, OO)/</)] (4.3) mean values generally range from about 1 to 4% with

....
o
(J 1.5

- o

15 30 45 60 75 90
Angle of Incidence (degrees)
Fig. 42. Reference values of the angular-dependence factor for electrons as a function of the angle of radiation incidence at a depth of3
mm in ICRU tissue substitute. 55
1.5
d= 10mm
L-
...,0
-u
0

Q)
u
c:
Q)
1.0

"'C
c:
Q)
c.
Q)
"'C
L- 0.5
.2
::J
0'1
c:
<

0.0
a 15 30 45 60 75 90
Angle of Incidence (degrees)

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Fig. 43. Reference values of the angular-dependence factor for electrons as a function ofthe angle of radiation incidence at a depth oflO
mm in ICRU tissue substitute.

only minor systematic shifts at large angles of especially at a depth of d = 0.07 mm, for electron
incidence and at low electron energies. energies higher than 2 MeV and for angles of inci-
dence, a. > 75°.
Reference angular dependence factors
(278) Reference angular dependence factors were Personal dose equivalent
derived at the three recommended depths in the
ICRU tissue using the evaluation procedure de- (279) ICRU Report 47 (Paragraph 4.3.2) suggests
scribed in PTB Report DOS-24 (Grosswendt and that the dose equivalent in an ICRU tissue slab
Chartier, 1994). The resulting reference factors are phantom, Hp,slab(d,a.), is a satisfactory surrogate for
summarised and shown in Figs. 41-43 for the four- the personal dose equivalent in the human torso.
element ICRU tissue substitute and the correspond- The reference conversion coefficients and angular-
ing numerical data are given in Tables A. 45-AA 7 in dependence factors given in the previous section are
Annex 2. As is apparent from the figures, R(d,a.) is thus considered to be adequate fluence to the per-
strongly dependent on the angle of incidence, a., sonal dose-equivalent conversion coefficients.

56
5. Relationships Between Quantities

5.1. Introduction Smaller differences are due to the different specifica-


tions of these two protection quantities with respect
(280) This section examines the impacts of recent
to organs and their respective tissue-weighting fac-
changes in the recommendations ofthe ICRP and the
tors, WT. There is no numerical difference between E
ICRU on both protection and operational quantities,
and HE because of changes in radiation weighting
discusses the interrelationship between these quan-
between the organ dose equivalents (evaluated using
tities and describes the performance of the opera-
the quality factor) and the organ equivalent doses
tional quantities as predictors of the protection
(evaluated using the radiation-weighting factor).
quantities.
The mean quality factor Q for photons is taken by
convention to be unity, the radiation weighting fac-
5.2. Changes in the Protection and tor is also defined as unity.
Operational Quantities (285) For all the irradiation geometries considered
in this report (AP, PA, LAT, ROT, and ISO), and for

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5.2.1. General all photon energies above approximately 20 keY, the
differences between HE and E are small. This is
(281) Section 2 has described those conceptual shown both in Fig. 44, which compares conversion
changes, modifications in specification and changes coefficients for E and HE in the AP irradiation
in physical data that affect the quantities used in the geometry, and in Fig. 45, which shows the ratios
dosimetry of external ionising radiations for radiologi- E I HE in all irradiation geometries.
cal protection. (286) For all irradiation geometries and for photon
(282) This section analyses the impact of these energies above 100 keY, the differences between E
changes on the protection quantities and operational and HE do not exceed 12%. However, for energies
quantities and their function with particular empha- between 25 and 100 keY (and in the PA and LAT
sis being given to: geometries), HE differs substantially from E, by as
• a comparison between the currently recom- much as a factor of 2. Over the energy range 10-100
mended ICRP basic protection quantity (the
keV the differences between the conversion coeffi-
effective dose, E) with that previously recom-
cie~ts for E and HE are smaller for the multidirec-
mended (the effective dose equivalent, HE) (Sec-
tional irradiation geometries (ROT and ISO) than
tion 5.2.2).
they are for the PA and LAT geometries (i.e., the
• A comparison between the currently recom-
ratios E I HE are more nearly equal to 1). At photon
mended values of the conversion coefficients for
energies above 1 MeV, the ratio EIHE is relatively
the operational quantities (ambient dose equiva-
unchanged with energy and approaches the value
lent, H*, directional dose equivalent, H', and
1.0 for all geometries. At the other extreme of the
personal dose equivalent, Hp), with those previ-
energy spectrum, as the photon energy falls below
ously recommended (Section 5.2.3).
about 20 keY, E may exceed HE significantly in some
irradiation geometries (see Fig. 45).
5.2.2. Protection quantities (287) The variation of the ratio E I HE with energy
is determined in a complex way by the irradiation
(283) This section considers the effects of the geometry, by the location of the organs and by their
changes in the protection quantities-from the dose tissue-weighting factors, WT. This is illustrated in
equivalent to the equivalent dose, and from the Fig. 7, which shows the organ equivalent dose conver-
effective dose equivalent to the effective dose (ICRP, sion coefficients for a few selected organs (the colon,
1977, 1991a). Whenever the term 'effective dose female breast, lungs, red bone marrow, and skin)
equivalent' is used in this section, it refers to the irradiated in the AP geometry as a function of
quantity defined in ICRP Publication 26. No modifi- energy. At low photon energies, the organ equivalent
cations of this definition are used to calculate any doses are much higher for superficial organs than for
other 'effective dose equivalent-like' quantities. deep-lying organs - the effect being most pronounced
for skin. For this reason, with the skin being in-
cluded in the specification for the effective dose but
Photons omitted for the effective dose equivalent, the effec-
(284) The principal reason for differences between tive dose is higher than the effective dose equivalent
effective dose and effective dose equivalent is the at very low photon energies in some irradiation
inclusion of skin in the specification of the effective geometries.
dose. The consequence of this change becomes par- (288) In AP geometry the enhancement of E as
ticularly evident at low photon energies (see Fig. 7). compared with HE, which arises from the contribu- 57
E (ICRP Publication 60)
Hs (ICRP Publication 26

~ 0.5
o
"d
4)

.::
...
..."

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~
~ O.Ou-~ __~__~~~~~L-__~__~~~~~~____~__L-~~~~U
0.01 0.10 1.00 10.00
Photon energy (MeV)
Fig. 44. A comparison of conversion coefficients in AP irradiation geometry for effective dose, E, and the effective dose equivalent, HE,
per unit air kerma free-in-air as a function of photon energy.

tion of the skin, is to some extent mitigated by the of the breast is reduced because its weighting factor
reduced weighting factor given to the breast-an is 0.05 (see Figs. 46 and 47).
organ that can also receive a significant dose in the (289) At energies above approximately 25 keY
AP irradiation geometry when irradiated by low- (when deeper organs are irradiated and therefore
energy photons (see, for example, the ratio of E / HE the influence of the doses to superficial organs and
in Fig. 45 at 10 keY for the AP irradiation geometry any changes to their weighting factors become ofless
as compared with the ratio in PA irradiation geom- relative importance), the numerical differences be-
etry). The female breast dose makes a significant tween the effective dose and effective dose equivalent
contribution to HE with a weighting factor of 0.15. In are largely due to two changes in the specification of
the effective dose, however, the relative contribution the remainder. First, and most importantly, ICRP

::r;'"

..
c AP
PA
-;: LAT
.;; 10 ROT
....
c-

'"
ISO

..
~
Q
'C

...
00 ~
en ~
en
.... .....
t-- ~
to ~ \ .
t;
0
P-
Q)
..
~
Q
'C
\
\
\
':
':
0:: ... 1
..... : .......... :...... :..................... .
~ ~

-
C)
~

0.01 0.10 1.00 10.00


Photon energy (MeV)
58 Fig. 45. The ratio E / HE for several irradiation geometries as a function of photon energy.
0.037 0.03 0.056 0.139
Bladder Lung Others Stomach
0.04
Skin
0.087 0.412 0.128
0.058
Stomach Testes Testes
Breast
0.066
Thyroid
0.147 0.121
Thyroid 0.08 Colon
0.191 Red bone
marrow Ovaries Lung
Breast

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IWTHTIHE]
0.021 0.01
Lung Red bone 0.038
0.062 0.017marrow 0.076 Thyroid 0.026
Thyroid Bone surface Red bone Bone surface
0.323
0.138 Remainder
Remainder 0.399 0.107
Breast Lung

0.112
Ovaries

Testes Testes Breast


Fig. 46. Relative contributions of specific organs to effective Fig. 47. Relative contributions of specific organs to effective
dose and to the effective dose equivalent respectively for 20 keY dose and to the effective dose equivalent respectively for 200 keY
incident photons in AP irradiation geometry on an adult human incident photons in AP irradiation geometry on an adult human
computational model. computational model.

Publication 60 reduced the tissue-weighting factor dose have changed, primarily because of the introduc-
for the remainder by a factor of6 compared with that tion of the concept of radiation weighting factors (see
given in ICRP Publication 26. Second, the remainder Sections 2.4 and 4.4.2 for further discussion).
dose contributing to HE is higher than that which (292) Conversion coefficients from neutron fluence
contributes to E because the former is averaged over to the effective dose are given in Section 4 for the
those five remainder organs that have the maximum standard irradiation geometries. Figure 48 shows
dose, whereas the latter is determined from the the ratio E / HE for four irradiation geometries (AP,
average of the doses to 10 fixed organs. PA, LAT, and ROT). In AP geometry, and for the
(290) The influence of geometry and WT on the energy range from thermal energies to 1 MeV, the
relative contributions to E and HE at 20 and 200 keY ratio E / HE varies between 2 and 4. The ratio steadily
may be seen in Figs. 46 and 47, in AP irradiation increases for PA geometry from about 1.5 at thermal
geometry.21 energies to a value of 4 at about 1 keY, then rises
steeply with energy between 10 keY and 200 keV, and
Neutrons has a value of 7-7.5 over a broad peak from 50-200 keV,
before declining to a value of! near 10 MeV. The energy
(291) The impact of the new specifications of the dependence of the ratio in the LAT and ROT geom-
protection quantities is most noticeable in the case of etries is similar to that for the PA geometry, with a
neutrons. As a result, the values of the conversion broad peak between 10 and 200 keY and maximum
coefficients from fluence to organ doses and the effective values of the ratio between 4 and 5. In all four
geometries, the value of E / HE is about 1 at 10 MeV.
(293) In summary, there are significant differences
21 It should be noted that the absolute values of wTHT are
different for HE and E (see the specifications in JCRP Publications
between E and HE for neutrons. These large differ-
26 and 60, and also the values of WT in Tables 1 and 3 in the ences are mainly due to the method of radiation
Glossary). weighting and the weighting factor used to calculate 59
AP
PA
LAT
6 ROT

o~~-L~~~~~~~~~~~~~~~~~
10-9 10'" 10-7 10"' 10-5 1~ 10.3 10-1 10.1 10° 101
Neutron energy (MeV)
.5 Fig. 48. The ratio E / HE for incident neutrons in several irradiation geometries on an adult human computational model (mean of

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~ values calculated in ADAM and EVA) as a function of neutron energy.
;:
,..
<2
!l
!'::
Q)
.<:j
the two quantities. In the calculation of HE, the 48. This may be best done by focusing attention on
!SQ) radiation weighting is achieved by using the Q(L )-L the differences between the values of WR and those of
o relation at the point of energy deposition. Thus, the mean quality factors, Q, for each organ. At 14
U
!':: weighting is applied to the absorbed dose deposited MeV, the value ofwR calculated from eqn (2.5) is 7.7.
.S
en by the degraded neutron spectrum and the induced In both the AP and PA geometry, the values for the
~
;> photon spectrum (see Sections 2.4 and 4.4.2 for a organ mean quality factors vary between 7.0 and 9.0,
!'::
o discussion). By contrast, the values of WR used to with the exception of the bone surface in the AP
U
calculate E are determined only by the neutron geometry. Thus, only small differences are to be
energy incident on the body and do not alter with the expected between E and HE in either geometry and
changing character of the nuclear transformations this is confirmed in Fig. 48. At 100 keY, however, the
occurring in the body. organ mean quality factors differ widely from one
(294) The differences between E and HE as the another, by organ and by irradiation geometry. Fur-
neutron energy and irradiation geometry change are thermore, the values of organ Q are substantially
shown in Fig. 49. This figure compares the relative different from the calculated value of WR of 16. In AP
contributions of specific organs to the effective dose geometry, for example, the mean quality factor for
equivalent, HE, and the effective dose, E, for the AP the ovaries used in the computation of HE is less than
and PAgeometries and at two energies. The energies 10% of the value of the radiation weighting factor
selected are 100 keY, in the energy region where the used in the computation of the effective dose, E; for
largest differences between the two quantities occur; the testes, it is 55%. Similarly, in PAgeometry at 100
and 14 MeV, where the differences are small. Data22 keV, the mean quality factors for the ovaries, testes,
showing the relative contributions of specific organs and breast are all less than 10% of the value of the
to the effective dose equivalent (HE) and effective radiation weighting factor used in the computation
dose 23 (E) are presented. For the effective dose of the effective dose.
equivalent, the separate values of the mean quality (296) From these discussions it may be deduced
factor, Q, are indicated for the constituent organs. that the difference between E and HE is greatest in
For the effective dose, the values of WR (which are PA irradiation geometry and for incident neutron
organ-independent) shown on the figure are calcu- energies around 100 keY, where moderated (slowed
lated from eqn (2.5). down) neutrons have smaller values of Qn than the
(295) Inspection of Fig. 49 permits a qualitative primary (uncollided) neutrons.
understanding of the ratios of E / HE as shown in Fig.

Electrons
22 Taken from JCRP Publication 51 for HE and from this report
for E (see the tables in Chapter 4). Values of mean quality factor (297) Inclusion of skin as an organ in the specifica-
for the breast, ovaries, and testes were obtained from Hollnagel
tion ofthe effective dose leads to differences between
(1994a).
23 It should be noted that the absolute values of wTHT are
the effective dose and effective dose equivalent.
different for HE and E (see the specifications in JCRP Publications These differences are only noticeable at relatively
60 26 and 60, and also in Tables 1 and 3 in the Glossary). low electron energies.
HE - AP 100 keY ([=7.1 E - AP 100 keY wR = 16

Testes Q=
.Kelmall'clerQ = 2.4

HE-AP 14 MeV ([=7.6 E-AP 14 MeV wR=7.7


Others
Ovaries 0= .RelmaillderQ = 7.4

Testes Q = 7.6 i~~~mriii

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Q=80

Bone M . 0 = 7.

HE - PA 100 keY ([=4.1 E - PA 100 keY wR = 16

Breast Q= 3.3
0=1.5

HE-PA 14 MeV ([=7.5 E - PA 14 MeV wR = 7.7


OIhc,"
Ovaries Q= 7. Rcn"uirldcrQ =7.3

Testes Q=7

Q=8.6
Q-78
Breast
Fig. 49. Relative contributions of specific organs to effective dose and to the effective dose equivalent for 100 keVand 14 MeV incident
neutrons inAP and PAirradiation geometry on an adult human computational model (mean of values calculated in ADAM and EVA).

(298) Schultz and Zoetelief (1996) have reported steeply as the electron energy decreases (Fig. 50).
calculations of the conversion coefficients for the Below 600 keV, the steep increase in EIHE is due
effective dose, E, using the MIRD phantoms (ADAM totally to the dose to the skin, which is not included
and EVA). These calculations, which were restricted in the specification of HE' At these energies, the dose
to the AP geometry, spanned the energy range from contribution of even the most superficial organs is
80 keV to 10 MeV. These authors have also reported more than two orders of magnitude lower.
new calculations of the conversion coefficients for HE
under the same conditions. There is good agreement
Sununary: changes in the
between the new conversion coefficients for HE and
protection quantities
those reported earlier in the literature.
(299) In AP geometry, and for electron energies (300) For photons and for most irradiation geom-
from 1.5 to 10 MeV, the ratio E I HE remains almost etries, the difference between conversion coefficients
constant at a value close to 0.7. At 1 MeV, the ratio for the effective dose, E, and effective dose equiva-
EIHE is approximately 1; below 1 MeV, it increases lent, HE, is typically less than 5%. At energies below 61
definitions of the operational quantities and in the
recommended values of the conversion coefficients
:5
(lCRU, 1992a,b). The precise definition of the direc-
tional dose equivalent, H'(d), has changed and a new
quantity, the personal dose equivalent, Hp(d), has
2 replaced the individual dose equivalent (penetrat-
ing) and the individual dose equivalent (superficial)
(lCRU, 1992a,b). These changes in definition re-
sulted in no numerical changes in the appropriate
conversion coefficients.
(303) Revised values for the stopping powers of
protons and 4He+ + ions given in ICRU Report 49
(lCRU, 1993a) influence the values of quality factor
100 (see Section 2.4.8).
Electron energy (MeV) (304) The recommendations of ICRP Publication
Fig. 50. The ratio E / HE for incident electrons in AP irradia- 60 also affect not only the protection quantities but
tion geometry on an adult human computational model (mean of also the operational quantities. Changes in the opera-

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values calculated in ADAM and EVA) as a function of electron tional quantities arise primarily because of the
energy. revised Q(L)-L relationship (ICRP, 1991a). No fur-
ther changes have been made in that relationship
25 keV, there are some significant differences (>30%) following the revision of the stopping powers. These
between E and HE because ofthe inclusion of skin in changes have implications for practical monitoring
the specification of the effective dose. This change and measurement but, in practice, the effect of these
makes the effective dose a numerically larger quan- changes on the values of the conversion coefficients
tity than the effective dose equivalent at low ener- for operational quantities is only significant for
gies. In the PA and LAT geometries, however, and at neutrons.
photon energies between 25 and 100 keV, E is less (305) This section compares the currently recom-
than HE by as much as a factor of 2. mended values of the conversion coefficients for the
(301) As intended by the ICRP, there are large ambient dose equivalent, directional dose equivalent
differences between the conversion coefficients for and personal dose equivalent with those given in
converting fluence to effective dose, E, and to effec- ICRP Publication 51 (ICRP, 1987). Differences be-
tive dose equivalent, HE, for neutrons. These differ- tween the older and newer data are discussed in
ences arise partly because of the choice of values of terms of changes in the recommended technique for
radiation weighting factors for neutrons and partly radiation weighting and of modifications in the
because, in the calculation of effective dose, the physical database used in the calculations.
radiation weighting factor is determined by the
energy ofthe incident neutrons, and is applied to the
absorbed dose in the organ or tissue, regardless of Photons. Ambient dose equivalent
the quality of the radiation in that organ or tissue. (306) The values of the conversion coefficients from
The quality factors used in effective dose equivalent air kerma to the ambient dose equivalent, H*(10), for
are determined and applied at the point of interac- photon energies between 10 keV and 10 MeV are
tion. The conversion coefficients for E for neutron given in Table A.21 in Annex 2. These values are not
energies up to 1 MeV are typically 2-4 times higher significantly different from those recommended in
than those for HE. This increase is consistent with ICRP Publication 51 (ICRP, 1987). The data adopted
the intentions of the ICRP. Under particular condi- are taken from the more recent ICRU Report 47
tions of energy and irradiation geometry, the conver- (ICRU, 1992a), in which several sets of published
00
sion coefficient for E can be as much as seven times data were evaluated.
Ol
Ol
,.....
larger than that for HE. At about 10 MeV and above,
the differences between the conversion coefficients
for E and HE are small «5%). Data at energies up to Photons. Directional dose equivalent
180 MeV are incomplete. (307) Although the definition of the quantity has
been slightly modified, the numerical values of the
5.2.3. Operational quantities conversion coefficients have not significantly changed
from those recommended in ICRP Publication 51
and ICRU Report 43 (ICRP, 1987; ICRU, 1988).
General Tables A.22 and A.23 in Annex 2 give values of
(302) Since the publication of ICRU Report 39 recommended conversion coefficients for H'(10,a)
62 (lCRU, 1985), there have been modifications to the and H'(0.07,a) for a range of values ofthe angle a to
H* calc. with Q(L) - ICRP 60 and ICRU 49 (liquid phase)
+ H* calc. with Q(L) - ICRP 60 (vapour phase)
x H* calc. with Q(L) - ICRP IS. 21 and 26 (vapour phase)
1~~~~~~~~~~~~~~~~~~~~-u~-u
1~ 1~ 1~ 1~ 1~ 1~ 1~ 1~ 1~ l~ t~
Neutron energy (MeV)

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Fig. 51. Conversion coefficients for H*(10)1<P for neutrons in AP irradiation geometry based on different Q(L) relationships and
stopping power in both vapour and liquid phases.

the principal axis of the ICRU sphere between 0° and (2) with the ICRP Publication 60 Q(L )-L relation-
180°. The quantity H'(3) is not widely used in ship and the stopping power data for water in the
practical monitoring for radiological protection and vapour phase; and (3) with the ICRP Publication 60
conversion coefficients are not given in this report. Q(L)-L relationship and the new stopping power
data for water in the liquid phase. The differences
resulting from the Q(L)-L relationship introduced
Photons. Personal dose equivalent
by ICRP Publication 60 are trivial at energies above
(308) Tables A.24 and A.25 in Annex 2 summarise about 1 MeV. The small differences below 1 MeV are
the values of Hp,slab(lO,a) and H p,slab(0.07, a) and the about 25% in the thermal to intermediate energy
corresponding angular dependence factors, R(d,a), regions, reaching a maximum of about 40% near to
as a function of the angle of incidence, a, of radiation 400 keY.
up to angles of 75° for photons. Pending calculations
in the human trunk for various irradiation geom- Neutrons. Directional dose equivalent
etries and photon energies, it is not possible to
estimate precisely how these surrogate conversion (311) Because neutrons are deeply penetrating,
coefficients, Hp,slab (d,a), mimic Hp(d) in the human values of the directional dose equivalent for neu-
trunk; but the errors involved are thought to be trons are of limited interest, and so no conversion
small (see Section 2.6.4). coefficients are given for this quantity for neutrons.

Neutrons. Personal dose equivalent


Neutrons. Ambient dose equivalent
(312) Under AP irradiation conditions in the fron-
(309) Since 1985, there have been two changes to tal hemisphere, the value of H p,slab(10, 0°) is very
the conversion coefficients for ambient dose equiva- similar to H*(10) (see Fig. 52 and Table A.42 in
lent: a new Q(L)-L relationship has been recom- Annex 2). For other directions of radiation incidence,
mended (lCRP, 1991a) and new stopping power data rough estimates may be achieved by applying data
for protons and alpha particles have been published for H p,slab(10,a). See Section 2.6.4 for a detailed
(ICRU, 1993a). A detailed discussion of these changes discussion of personal dose equivalent.
is given in Section 2.4.8, and their consequence may
be seen in Fig. 51.
Electrons. Directional dose equivalent
(310) Figure 51 shows the neutron fiuence to
ambient dose equivalent conversion factors obtained (313) Comparison between recently calculated nu-
with both the Q(L) relationships (ICRP, 1977; ICRU, merical values and the values presented in ICRP
1993a) and stopping power data for both water Publication 51 and ICRU Report 47 shows that there
vapour and liquid water (lCRU, 1993a). The three are no significant differences between the new and
curves presented are (1) with the Q(L)-L relation- older data. The reference values recommended in
ship used in ICRP Publications 15, 21 and 26 and the this report result from an extensive analysis of data
stopping power data for water in the vapour phase; provided by several authors. This analysis also in- 63
E I H*(10), (lCRP 60)
E I H,(10), (lCRP 60)
1.5

,------'"
0.5

O~~~~~~~~~~~-L~~~~~~~~-W

10-' 10-8 lIT7 104 10-5 10~ 1003 10-1 lIT1 10° 101 101
Neutron energy (MeV)

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.5 Fig. 52. The ratios of effective dose, E, to H *( lO ) and Hp,slab(lO,OO) as a function of neutron energy.

cluded an estimate of the uncertainties in the refer- 49. At energies below 1 MeV, the conversion coeffi-
ence data. Table A.44 in Annex 2 gives values of cients for H *(10) are typically 20-40% higher than
conversion coefficients from electron fluence to those given in JCRP Publication 51. At energies
H'(0.07,a), H'(3,a), and H'(10,a) for values of a = 0°, above 10 MeV, there are no significant differences
where a is the angle to the principal axis ofthe ICRU between the data sets. For personal dose equivalent,
sphere. Tables A.45 to A.4 7 give values ofthe angular there are concomitant changes in the conversion
dependence factors that facilitate calculation of coefficients.
H'(0.07,a), H'(3,a), and H'(10,a) for the value of a in
the range 0° :=:; a :=:; 90°.
5.3. Relationships between the Protection
and Operational Quantities:
Electrons. Personal dose equivalent The Performance of the
Operational Quantities
(314)As is the case for photons, data calculated for
ICRU phantoms may serve as surrogates for the
5.3.1. General
personal dose equivalent. The data for H'(d) calcu-
lated in the ICRU sphere and slab do not differ (317) The operational quantities were designed to
significantly from each other; therefore, the data for facilitate measurements that provide an adequate
H'(d) in Table A.44 may also serve for Hp(d) in the approximation to the appropriate protection quan-
human trunk. Section 2.6.4 provides a detailed dis- tity for irradiation from external radiation sources,
cussion of the personal dose equivalent. while avoiding underestimation or excessive overes-
timation of the quantity. Before the changes in the
recommendations of JCRP Publication 60, it was the
Summary
case that" . .. for neutrons and photons over a wide
(315) In the case of electrons and photons, the energy range, and for electrons present in routine
differences between the conversion coefficients for operations, these aims are usually met by the deter-
the ambient and directional dose equivalent given in mination of the dose equivalent at certain specified
this report and those previously published in JCRP depths in the ICRU sphere" (ICRU, 1985). Changes
Publication 51 and JCRU Report 43 are small (less in both the ICRP and ICRU recommendations over
than 5%). Conversion coefficients for the personal the past 10 years have directly affected the opera-
dose equivalent for photons and electrons incident tional quantities. Thus, it is important again to
on the human trunk are not available but it is establish whether the operational quantities con-
assumed that their values are close to those obtained tinue to provide an adequate measure of the ICRP
from calculations of the dose equivalent in the protection quantities.
tissue-equivalent sphere and slab phantoms. (318) The performance of the operational quanti-
(316) For neutrons, there are some changes in the ties as predictors of the protection quantities is
conversion coefficients for the ambient dose equiva- described in this section. This is done by examining
lent because ofthe new Q(L)-L relationship in JCRP the relationships between the protection quantities,
64 Publication 60 and stopping powers in JCRU Report particularly the effective dose, and those operational
OverelTimation

O~~~~~-L~~~~-L~~~~-L~~~U
10-9 10-8 10-7 10"' 10-5 10-4 10.,] 10-2 10-1 100 101 102

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


Neutron energy (MeV)
Fig_ 53_ The performance of a mbient dose equivalent H *( lO ) as indicator of effective dose for neutrons in AP irradiation geometry.

quantities used for area and individual monitoring with H*(10) because this quantity is defined in
(i.e., the ambient dose equivalent, directional dose an aligned field , and therefore conversion coeffi-
equivalent, and personal dose equivalent). These cients for H*(10) are the same in all geometries.
relationships are discussed for photons, neutrons, E(AP) can also be compared with H'(10,00) and
and electrons; the conversion coefficients of this H p,slab(10,00) because conversion coefficients for
report are used throughout this discussion, unless these quantities correspond to radiation incident
stated otherwise. at 0° to the principal axis of the ICRU sphere and
(319) The operational quantities were designed to to the front ofthe ICRU slab, respectively.
provide a reasonable estimate of the appropriate • PA geometry: E(PA) denotes the conversion coef-
protection quantity under normal working condi- ficients for effective dose from fluence or air
tions. For external irradiation of the body, this may kerma in PA geometry. E(PA) can be compared
be simply expressed by the goal that the value of the directly with conversion coefficients for H * (10),
appropriate protection quantity is less than that of which are independent of radiation geometry
the operational quantity. It must be emphasised that (see above). E(PA) can also be compared directly
this goal applies to radiation fields to which people
with H'(10,1800) and Hp,slab (10,180°) because
are exposed and these fields are usually associated
conversion coefficients for these quantities corre-
with broad energy spectra and various irradiation
spond to radiation incident at 180° to the princi-
geometries.
pal axis ofthe ICRU sphere and to the front face
(320) As an example, Fig. 53 illustrates the perfor-
of the ICRU slab, respectively. Hence the dose
mance of the ambient dose equivalent, H * (10), in
equivalent is calculated at a depth of 10 mm in
estimating effective dose, E, from neutrons in AP
geometry. The ratio of conversion coefficients from ICRU tissue, at a point opposite the incident
fluence for neutrons (similar figures will be pre- radiation, which has to travel through the bulk
sented for photons and electrons) is calculated for a of the tissue equivalent sphere (290 mm) or slab
range of radiation energies and geometries. In those (140 mm).
energy regions where E / H * (10) exceeds unity, the • LAT geometry: E(LAT ) denotes conversion coeffi-
protection quantity is underestimated by the opera- cients from fluence or air kerma in LAT geom-
tional quantity. Conversely, where E / H*(10) is less etry. E(LAT) can be compared directly with
than unity, the operational quantity will provide an conversion coefficients for H*(10), which are
overestimate of the protection quantity. independent of radiation geometry. E(LAT) can
(321) In order to ensure valid comparisons of also be compared directly with H'(10,900) be-
protection and operational quantities, a convention cause conversion coefficients for this quantity
has been adopted to distinguish values of conversion correspond to irradiation at 90° to the principal
coefficients for quantities in different irradiation axis of the ICRU sphere. Conversion coefficients
geometries. for H p,slab(10,900) are available but there are
• AP geometry: E(AP) denotes the conversion coef- some uncertainties in published data. In any
ficients for effective dose from fluence or air case, the validity of comparing E(LAT) with
kerma, in AP geometry. E(AP) can be compared Hp,slab data is questionable, because it is not 65
P ROTECTlON O PERATIONAL QUANTITIES

G EOM ETRY QUANTITY AREA MONITORING I NDlVIDUAL MONITORING

AP E (AP) H* ( lO ), H '(10 ,OO) H p ,slab(10 ,OO), Hp,organ(AP)


PA E(PA) H* ( lO ), H '( lO,1800) H p,slab(lO,1800), Hp,organ(PA)
LAT E(LAT ) H*(lO), H'(lO ,900) slab data not valid, Hp,organ(LAT)
ROT E(ROT) H*(lO), H'(lO,ROT) Hp,slab(lO,ROT), Hp,organ(ROT)
ISO E(ISO ) H*(lO) , H'(lO,ISO) no slab data exist, Hp,organ(ISO)

likely to correspond closely to Hp(d) in the body gate measures of Hp(d) in the body, particularly for
for LAT geometry, comparisons with Hp,slab(d),
• ROT geometry: E(ROT) denotes the conversion (323) In summary, the comparisons made ofprotec-
coefficients for effective dose from fluence or air tion and operational quantities and correspondences
kerma in ROT geometry, E(ROT) can be directly made for particular irradiation geometries are shown
compared with conversion coefficients for H * (10), in the table above,
which are independent of radiation geometry.
E(ROT) can also be compared with H'(10,ROT)

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5.3.2. Area monitoring
and conversion coefficients for this quantity are
obtained for dose equivalent at a 10 mm depth in
Photons
the ICRU sphere in a 360 0 rotating plane paral-
lel beam (lCRP, 1987), Furthermore, E(ROT) can (324) The relationships between the effective dose,
be compared with H p,slab(10,ROT). Conversion E , and ambient dose equivalent, H*(10), can be seen
coefficients for this quantity can be obtained in Figs. 54 and 55, which show, respectively, the
from values for H p,slab(10,a), where a is the angle values of conversion coefficients for the quantities E
of incidence of a plane parallel beam on the front and H *( 10), and the ratio E / H *(10) as a function of
face of the ICRU slab. For the purposes of this photon energy for the irradiation geometries AP, PA,
comparison, H p,slab(10,ROT) has been obtained and ROT, Inspection of these figures shows that
by averaging H p ,slab(10,a) for a = 0° to 360 0 at 15° H * (10) always overestimates E [i.e., E / H *( lO) < 1]
intervals (Till et al., 1995), for photons with energy up to 10 Mev'
• ISO geometry: E (ISO) denotes the conversion (325) For photon energies between 60 keV and 10
coefficients for effective dose from fluence or air MeV, the value of the ratio of E / H* ranges from 0.75
kerma in ISO geometry. E(lSO) can be directly to 0.92 for the AP geometry and from 0.48 to 0.85 for
compared with conversion coefficients for H*(10), the ROT geometry (see Fig. 55), Hence, the ambient
which are independent of radiation geometry. dose equivalent provides an overestimate of the
E(ISO ) can also be compared with H'(10,ISO) effective dose exceeding 15% for a wide range of
and conversion coefficients for this quantity are photon energies and irradiation geometries. At low
obtained for dose equivalent at a 10 mm depth in photon energies, the extent of overestimation is
the ICRU sphere in a fully isotropic radiation significant; at 25 keV, the ratio E / H*(10) is approxi-
field (ICRP, 1987). No data for H p ,slab(10,ISO) are mately 1/3 for the AP geometry and approaches an
available for photons, electrons or neutron radia- order of magnitude for the ROT and PA geometries,
tions , It is important, once again, to comment that, at low
(322) In addition to comparisons of effective dose photon energies, the dose to the skin and the lens of
values with personal dose equivalents in the ICRU the eye are of greatest importance in radiological
slab, Hp,slab(d), it is helpful to see how this latter protection (see Section 4.5.2) and, in this situation,
quantity corresponds to Hp(d), defined in soft tissue the quantities E and H *(10 ) are of limited practical
below a specified point in the body. Unfortunately, no application.
data exist for H p(d ) at the time of going to press, so
approximations have to be made. Hence, for the
Neutrons
purposes of comparing likely values of Hp(d) in soft
tissue in the body, dose equivalents in small organs (326) Figures 56 and 57 show the relationship
near to the surface of the body have been calculated, between the effective dose, E , and the ambient dose
using the absorbed dose data for photons and ab- equivalent, H *( 10). Up to incident neutron energies
sorbed dose and the Q-L relationship for neutrons. of 40 MeV, the ambient dose equivalent overesti-
In particular, dose equivalents to the thymus and mates the effective dose for all geometries, except for
testes are deemed suitable for this purpose and more the AP and PA. Above 40 MeV, H*(10 ) underesti-
details about these calculations are given later. mates E in all geometries. In the AP geometry, the
Conversion coefficients are denoted Hp,organ (geom- ambient dose equivalent underestimates E in energy
66 etry) and these are used to provide additional surro- regions from about 1 eV to 40 keV; from about 3 MeV
2.0 r-------------------------------..
-- H*(IO)
---- E(AP)
;;: •••••••• E(PA)
~ -.-. E(ROT)
;..
1.5
,- .
~ " ... "" '"
:J
...c
'y ,, " .... ", ..........
I.:
~ ,. ........... . ......... ---------------------.
..
o
C
1.0
"
I
J:,,'l-. -. -:........... ................. wy
--- ..............................:.:.:-.-.-
- - . - . __ . - .
.• .... - - _ ...

o I I
-E! : I
...;.. I ~

15 0.5 ,, t
-:
U : I!
" ,;!
" .~~ ..
."". -: "
-'!:...','

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


0.0 ~.J~.....~--I- .............................i..I.-:---........-"'---'-........................J-:-----'---'-........-'-.........-.....J
10 10" 10° 10'
Photon energy (MeV)
Fig. 54. Conversion coefficients for ambient dose equivalent and effective dose in various irradiation geometries as a function of photon
energy.

to 13 MeV; and above 40 MeV. E is also underesti- of neutron spectra (Bartlett et aZ., 1992; Posny et aZ.,
mated in the energy region from about 10 eV to 20 1992; Clark et aZ., 1993; Marshall et aZ., 1994). These
keY for the PA geometry, but the magnitude of the studies show that, at facilities in the nuclear indus-
underestimation is much less than is the case in the try (e.g., nuclear power plants and fuel-reprocessing
AP geometry. plants), the typical neutron spectra show peaks in
(327) In practice, irradiation by monoenergetic the energy range between 100 keVand 1 MeV, which
neutrons rarely occurs. Thus, it is necessary to is characteristic of degraded fission neutrons. In this
consider irradiation by neutrons distributed over a energy region, the ratio of E / H*(10) indicates that a
wide range of energies. Under these circumstances, measurement of H*(10) is likely to overestimate E in
the ambient dose equivalent is usually a conserva- all irradiation geometries. There are exceptions to
tive (safe) estimate for the effective dose. this general conclusion, especially when there are
(328) Several authors have studied the practical significant numbers of neutrons at energies below 10
implications for radiological protection for a variety keY, but these situations are rare.

10.00 r----------------------------,

1.00
,. .... ~.~.:.~.~.~.~.:••• ::'••• ~.r.~.::'••• ::'.r.r.r." ........ _ .. ____ - - -

-",'
,"
.-'l
,",,
0.10
. ..,,
.. '
" \.
,......,.-,'
,
, I - - E(AP) I H*(IO)
,, '
' •• - - E(PA) I H*(IO)
,, ' '
.. , ........ E(ROT) I H*(IO)

Photon energy (MeV)


Fig. 55. The ratio of E I H*(lO) for various irradiation geometries as a function of photon energy. 67
AP
PA
R·LAT
L-LAT
ROT
ISO

O~~~~~~~~~~~wA~~~~~~~~~~

10.9 10-8 10.7 10-6 10.5 10-4 10.3 10.2 10.1 10° 10 1 102

Neutron energy (MeV)


Fig. 56. The ratio of E / H*(lO) for several irradiation geometries as a function of neutron energy.

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


(329) When typical calibration sources are used in always highly recommended if reliable results are to
the workplace, calculated E / H*(10) ratios show that be obtained.
H*(10) should provide a reasonable overestimate of
E. In the AP geometry, for example, the ratio E /
H*(10) in a 252Cf spectrum moderated in a 400 mm 5.3.3. Individual monitoring
diameter sphere consisting of heavy water is 0.91; in
the unmoderated 252Cf spectrum, the ratio is 0.88; Photons. Effective dose and personal dose
and in the fairly 'hard' Am-Be source spectrum, the
equivalent
ratio is 1.05.
(330) In contrast, however, there are some environ- (331) Figure 58 shows the conversion coefficients
ments where high-energy radiations are present for E and H p ,slab(10,00) in AP geometry. E(AP) is
[e.g., in the cabins of high-flying airplanes or near compared with H'(10,00) and H p ,slab(10,00), because
high-energy accelerators where it might not be ad- conversion coefficients for these quantities corre-
equate to assume that H*(10) is a prudent measure spond to radiation incident at 0° to the principal axis
of effective dose] and higher values of depth, d, in ofthe ICRU sphere and to the front face of the ICRU
H*(d) may be appropriate. Knowledge of the neutron slab, respectively. Values for H*(10) are also included
spectrum in which measurements are to be made is in Fig. 58 for comparison. At ex = 0°, H'(10,00) is

E I H*(10), (lCRP 60)


E I H,(10), (lCRP 60)
1.5

0.5 ... --------------------------------.


----................

------ HE I H*(10), (ICRP 26 and 51)


O~~~~~~~~~~~~~wA~~~~~~~~

1~ 1~ 1~ 1~ 1~ 1~ 1~ 1~ 1~ 1~ 1~ l~
Neutron energy (MeV)
Fig. 57. The ratio of E / H*(lO) (solid line) and E / Hp,slab(lO) (dashed line) as a function of neutron energy. E is calculated for incident
neutrons in AP geometry on a human computational model; both E and H*(lO) are calculated as specified in ICRP Publication 60. For
68 comparison, the ratio HpfH*(lO) (lower dashed line) is also shown.
2.0 r---------------------------------------------------~
,"'- ..... .. .. E(AP)
,...,'..........."
" Hp,sIab(IO.OO)
:;:: I.
-.'. ",
• •••• " " H*(lO). H'(IO,OO)

-..
~ I.S

til
'-'
/
I
/
i
t
",-

-. ...
....... .....
.......::::- ...
...:-.,..........
I ~-¥u~~~~~~~~~~_~ _ _ _ ~
I
I
I
I
I
I
I
I
I
I
I
I
I
I
I

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


,,
I
I

0.0 ":.2:"""''---'---'---'--'-.L...J...........!..:----'----I.-1...-J'-'--'-''-I..I-::----I.--'-'-'----'--'-..........w
1
10 10. 10° 10 1
Photon energy (MeV)
Fig. 58. Conversion coefficients for operational quantities and effective dose as a function of photon energy in AP irradiation geometry.

equal to H*(10). For all photon energies up to 10 cate that it is likely that H p (10) may underestimate
MeV, Hp,slab( 10,0°) overestimates E to about the same the effective dose for photons of energy up to 1 MeV
degree as does H*(10). Figure 59 shows the ratio or more, At low photon energies, the magnitude of
E / H p,slab(10,00) for the same energy range. the underestimation may be very large but it should
(332) In PA geometry, it is assumed that be noted that this corresponds, in a practical situa-
H p,slab(10,1800) will provide a close measure ofH p (10) tion, to wearing a personal dosemeter at the front of
in the human trunk. Figure 60 shows conversion the body when irradiation is incident primarily at
coefficients for E, H p,slab(10,1800), H*(10), and the back. Underestimation of effective dose is there-
H'(10,1800); Fig. 61 shows the ratios E / fore to be expected in such a situation.
H p,slab(10,1800) and E / H'(10,1800). These ratios indi- (333) In LAT geometry, there are particular prob-

10,0

til
~
''':: - - E(AP) / Hp.•lab(IO,OO)
''':: - - - - E(AP) / H'(IO,OO)
=
co:
::s
C"
c;
=
c
'''::
co:
'Co"'
~
1.0

--=
c
c

.~
.-------------

-( .I
~

c
'Co"'
o..
C

-
,~

~
co:
0.1 ·2
10 1~ 1~
Photon energy (MeV)
Fig, 59. The ratios E / Hp,slab(lO,OO) and E / H'(lO,OO) as a function of photon energy inAP irradiation geometry. 69
2.0 r-------------------------------------------------~

-- E(PA)

- :l···············..... ----
••••••..
H p (10)
H*(10)
~ 1.5
--....
/ , '. - • _. H'(10,1800)
: .'.

..................................~:.~.:.:.:.:.:...................
t:'-I

.•=
u
to:
CJ

10-0 1.0
CJ
o
U

.•=o -.- .. ---


.. ......... .....
'
..........
t:'-I
~ 0.5
:.:
, . -- .... ----.- .......... ~ '
>
=
o . ,,
/

.. .....
..... ;'
;

U ......... . '

_...... _.... -.
'

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0.0 ~----~~~~-~.~-~.~-~.~~----~--~~~~~~----~--~~~~~~
.1
10 10,1 10°

Photon energy (MeV)


Fig. 60. Conversion coefficients for operational quantities and effective dose as a function of photon energy in PA irradiation geometry.

lems in comparing calculations of the effective dose equivalent at ex = 90° is therefore used for compari-
with Hp(d). First, until recently, available data for sons with effective dose in LAT geometry. Figure 62
the dose equivalent in the ICRU slab have been shows values of conversion coefficients for E(LAT)
unreliable for ex> 75° (Ambrosi et al., 1991). Second, and H'(10,900) together with H*(10) for purposes of
it is questionable to use H p ,slab(10,900) data for comparison. The conversion coefficients show that,
comparisons with effective dose because, at ex = 90°, for most photon energies, H'(10,900) is a good mea-
the difference in phantom geometry between a slab sure of E(LAT). This may also be seen in Fig. 63 from
and the human body is extreme. The ICRU sphere is the plot ofthe ratio EI H'(10,900) .
used instead, because such differences in phantom (334) In ROT geometry, data are available for the
geometry are much less obvious; directional dose dose equivalent in the slab, Hp,slab(lO,ROT), and in

100.0 ~--r--\--------------------,

'"
:~
-=
0:
............. .
=
c:r - - E(PA) / H p,slab(10,1800)
-; "".. - - - - E(PA) / H'(10,1800)
c 10.0 .. .
-...
.S
0:
u
c.
.... --.
co -
0
0 --- -. -- ---
O'l
O'l
,.....
C
.S - .... _- .. -- ... _-
uu
[:".'-
lC
....,
....0
0.
-...
0

...
C.
1.0 '-

~ 0

~ .S
>z:: ';
~ cz:
I I
0.1 ·1 I
10 10.1 10° 10
Photon energy (MeV)
70 Fig.61. The ratios E / H p ,slab(10,1800) and E / H '(1 0,1800) in PAirradiation geometry as a function of photon energy,
2.0

.-.
.../ .................
;.-.

---
C"..:)

en
;.-
1.5

j!
.: '-. '.

...............................
C
VI

Col
'u
.. .................... ~ ............................. .

S 1.0 _.- .. .,.. _.. _.. _.. _.. - .. -- - - .--


Col
o
.... ..... -_.- .-.-.-.-.
o
C ,. ....
';;;
...... ; /
~ 0.5
o - - E(LAT)
U
. ....•••. H*(10)
_. _. H'(10,900)

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0.010~·1~--~~~~~~~~1~0·-I----~--~~~~~1~0~O----~--~~~~~1~01

Photon energy (MeV)


Fig. 62. Conversion coefficients for operational quantities and effective dose as a function of photon energy in LAT irradiation
geometry.

the sphere, H'(lO,ROT). These data can be compared these energies, there is some appreciable overestima-
with conversion coefficients for effective dose. The tion of E by the operational quantities.
sets of conversion coefficients are shown in Fig. 64 (335) In ISO geometry, conversion coefficients are
with data for H*(lO) included for comparison pur- available for the dose equivalent in the ICRU tissue-
poses. It can be seen that, in this geometry, Hp(d) is equivalent sphere but not for the slab. Figure 66
likely to provide a very good measure ofthe effective shows the conversion coefficients for E(lSO), H*(lO),
dose. The ratios E / Hp,slab( 10,ROT) and E / H' (lO,ROT) and H'(lO,ISO). The data show that Hp(d) is also
given in Fig. 65 emphasise the closeness of this likely to be a good measure of E in this irradiation
match for photon energies above about 40 keV. Below geometry for photon energies above about 40 keV.

10.0
VI
.!:!
~
=
C'I
:I
C'
-;
c
-......
.2
C'I

c.

--
0
0

.2
c
1.0
- 00

'"'"
-
.-<

.......
...c.
0

...
0

-
.2
~
C'I - - E(LAT) I H'(10,900)

0.1
10.1 I~ I~ 10
1

Photon energy (MeV)


Fig. 63. The ratio E(LAT)IH'(lO,900) as a function of photon energy. 71
2.0 r----------------------------------------------------------,
_E(ROT)
.......
.....-.
-....
~ I.S
.
.:.
".
....
- - - - Hp,JIab(IO,ROT)
•••••••. H·(IO)
_. _. H'(IO,ROT)
--re> .:
I -.
-.. ..

/ . . . . . . . . -.~:.~~~~:.~=~~~.~~~~~~.
~

.:l
cGJ

.:. :
'u
IS 1.0
GJ
o
<oJ - .. _-----_ .. ---
C
o
.~

U
u
~ O.S
o

:
i
I t
~..

./~/

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0.0 e·"
10.2 10.1 10°
Photon energy (MeV)
Fig. 64. Conversion coefficients for operational quantities and effective dose as a function of photon energy in ROT irradiation
geometry.

Below these energies, however, there is likely to be E, and personal dose equivalent calculated in a slab
some substantial overestimation of E by the opera- phantom or a sphere phantom (directional dose
tional quantities as is shown by the ratio equivalent). To establish whether these dose quanti-
E / H'(lO,ISO) in Fig. 67. ties are reasonable approximations to Hp(d) defined
in soft tissue in the body, comparisons may be made
with the average doses to small organs located near
Approximations to Hp for photons
the surface of the body (e.g., the thymus and testes).
(336) In the immediately preceding sections, com- In the absence of definitive calculations of Hp(d) in
parisons have been made between the effective dose, the human trunk, equivalent doses to some small

10.0
<II
GJ
'';:
'';:
c
"=
='
-;
0
c
~

"
J..
GJ
Co _.... ---._-----._---_._-- ..
-
0
0
0
1:1
1.0

-e
~
<oJ
~

....
Co
0
0
- E(ROT) I Hp,slab(IO,ROT)
'';: - - - - E(ROT) I H'(IO,ROT)
"
r:z::
0.1
10.2 I~ I~
Photon energy (MeV)
72 Fig.6S. The ratios E / Hp,slab(ROT) and E / H'(lO,ROT) as a function of photon energy.
2.0 r-----------------------------,
,_ .. ,
,, .. ...
~
.....15 , I ...
..
Co:)
~ ,,
, " .. ..... .
CIl
'-" ,, ' .... , ..........
.l!l I' .... - ......
'y
=
Q,j

,
I - ...... ------------ ..
E 1.0
Q,j
o
Col
,... .,.......................................................................................
.~
=
o
Q,j /' /.l/
~ 0.5
o - E(ISO)
U
,'........../ - - - - H*(IO)

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•••••••. H'(IO,ISO)
, .'
0.0 .] .-
, , " .'
·1
10 10 10°
Photon energy (MeV)
Fig. 66. Conversion coefficients for operational quantities and effective dose as a function of photon energy in ISO irradiation geometry.

organs, appropriately located in the body, can be LAT and ISO geometries. Figure 69 shows the ratios
assumed to be approximations to the point quantity for E I Hp,thyrnus for the same geometries as in Fig. 68.
Hp(d) and are referred to in what follows here as The ratios and their general trends, both with re-
Hp,organ, where the term organ refers to the organ spect to energy and irradiation geometry, are very
used as a surrogate for the human trunk. similar in the two figures. However, it must be
(337) The validity of this expedient in the case of stressed that because Hp,thyrnuS is an approximation
photons may be partially inferred by comparing the for Hp(d) in the human trunk, only qualitative
data in Figs 68 and 69. In Fig. 68, the ratios of conclusions should be drawn from these two figures.
conversion coefficients E I Hp,slab(lO) are given for the (338) From these comparisons, it seems likely, for
AP, PA, and ROT geometries and of EI H'(lO) for the those photon irradiation geometries generally found

10.0

til
Q,j

-=
:=
=
=
co
-;
=
.2
..
c:;
G.I
Co

-
0 1.0
0
00
= 0>

--e
.2
Col
G.I
0>
.....
~
U";)

1::
0
....
Co
P-
C>
C>
~
.::: - - E(180) I H'(IO,ISO) ;:J
... p::
~

0.1 .J ·1 1
-
CJ

10 10 10° 10
Photon energy (MeV)
Fig. 67. The ratio E(lSO)IH' (1 O,lSO) as a function of photon energy. 73
100.0
,, -- E(AP) I Hp,slab(IO,O·)
-.:::'" ,,
u
---- E(PA) I H ......b(10,180·)
-.::: , ........ E(LA T) I H'(IO,90·)
1:1
<'I
,,
=
C'
,, -. -.
_ .. - •.
E(ROT) I H ....lab(lO,ROT)
E(ISO) I H'(10,ISO)
-; ,
1:1 10.0 \
,
C>
-.:::<'I .
-
\

\
U
C. \

- C>
C>
1:1
C>
-.:::u . ~
\
, ....
.... -._- -._-- ....
-- .....
-eu

c.
....
C>
1.0

,~ " "
,-:.=:.::.:.-:-'- _._.:::::::::::::. --:.- --
." .•.-!..... ..... _...........•......................•............

-
"
.~
<'I

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~

0.1 ~_l~--~--~~~~~~~--~--~~~~~~~--~--~~~~~WW
1 1
10 10- 10° 10
Photon energy (MeV)
Fig. 68. The ratiosEI Hp,slab(lO) and E I H'(lO) for several irradiation geometries both as a function of photon energy.

in the workplace and environment (AP, ROT, and (341) In theAP geometry, the ratio ofEIH p,slab(10)
ISO), that Hp(d) in the human trunk will either be a is very similar to the ratio E I H *(10) (see Fig. 57).
close measure of the effective dose or provide a Comparisons between E and Hp,slab in geometries
reasonable overestimate. This conclusion also ap- other than the AP are fraught with difficulty and
pears to be the case in LAT geometry.24 In the PA require great care in the interpretation of the data.
geometry, however, it appears likely that Hp(d) in Nevertheless, there is a practical need to know the
the human trunk will considerably underestimate E value of the ratio E I H p (10) in geometries other than
over a wide photon energy range. This latter conclu- the AP so that the extent of the error in personal
sion is not unexpected and corresponds to the practi- dosimetry resulting from the incorrect placement of
cal situation where a personal dosemeter is worn in a personal dosemeter or by irradiation from an
the front of the body, which is primarily irradiated unexpected direction can be estimated. There are
through the back (see also Paragraph 332). reasons to believe that there is the potential for
(339) In summary, by contrast with the ambient H p,slab(10) to underestimate E for neutron energies
dose equivalent (which overestimates E in all irradia- between 1 eV and 50 keV.
tion geometries) we may infer that Hp(d) will provide
an overestimate or a close measure of E in the AP
and ROT geometries but could underestimate E in Approximation of Hp for neutrons
the PA irradiation geometry.
(342) As with photons, it is possible to make some
general observations by determining equivalent doses
Neutrons. Effective dose and personal to small organs close to the surface of the body. The
dose equivalent thymus and male gonads (testes) are of a suitable
(340) In lieu of definitive data for conversion size and are located at a suitable depth for the
coefficients for Hp(d) in the human body or suitable purposes of inferring the result of more precise
anthropomorphic phantoms, calculations have been calculations. Figures 70 and 71 show the ratios of
carried out for the dose equivalent in the ICRU E I Hp,testes and E I Hp,thymus, respectively, for several
tissue-equivalent sphere and slab phantoms for dif- irradiation geometries_ The dose equivalents in each
ferent geometries. organ were calculated in the human adult computa-
tional models (ADAM and EVA) using the Q(L )-L
relationship from ICRP Publication 60. As might be
expected, from the anatomical location of the organs
24 Although Hp.slab(10) and Hp,thymu s appear to have some
similarities in their energy variation in LAT geometry in the case and the sensitivity of the organ absorbed dose on
of photon irradiation, this similarity is unlikely to hold true for neutron scattering, the curves for the two organs are
74 neutrons. far from identical. They are nevertheless suggestive
100.0 , . . - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - .
E / Hp.u.ym ••
--AP
•••• PA
.. ·· .... LAT
-.-. ROT
_ .. _ .. ISO
,
,,
, ,

\. \"......................
\
.. ,,-----
\
..
~
----- ... _-- - .. - .........
--.-.----- .. _.. -':~

-- ;i:"W:-: .. ,.. ........... ",._ .... ,. ..


• " ' . , . _ _ JIo . . . . . .· . _ " ' . " ' • • .A.- . -

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I I
0.1 ~~~-~--~~~~~~.-I----~--~~~~~~o----~--~~~~-wUI
10 10 10 10
PhotOD eDergy (MeV)
Fig. 69. The ratio E / Hp,thymus for several irradiation geometries as a function of photon energy.

that, in the AP geometry, the personal dose equiva- Electrons. General


lent may prove to be an adequate measure of the
(344) There are few calculations available for
effective dose; but in other geometries, there is the
effective dose, E, from electrons and comparisons
possibility of serious underestimation of E by the
with operational quantities are difficult. The great-
personal dose equivalent H p (10). These tentative
est practical interest is in the comparison of direc-
conclusions serve to emphasise the importance of
tional dose equivalent, H'(0.07), with skin dose. The
well-designed calculations of Hp(d) in the human
data currently available only permit the comparison
body models or suitable computational models. At
between Hp,skin in AP geometry and H'0.07,00) or
the time of writing, preliminary calculations of Hp(d)
H p ,slab(0.07,00).
in a pseudo-organ situated at mid-torso in the anthro-
pomorphic phantoms (ADAM and EVA) have been
brought to the notice ofthe Task Group in the form of Electrons. Skin dose and directional
a personal communication but further work is needed dose equivalent
before definitive advice can be developed.
(345) The relationship between skin dose, Hp,skin>
and directional dose equivalent, H'(0.07, 0°), is given
in Fig. 72. The operational quantity provides a
Neutrons. Skin dose and directional considerable overestimate of skin dose at low elec-
dose equivalent tron energies. However, between 0.5 and 10 MeV the
(343) In general, for neutron irradiation,25 operational quantity provides a reasonable estimate
H'(0.07) < H'(3) < H'(10), and thus if the limit for of mean skin dose (within a factor of 2). At the
the effective dose is maintained, the limits for the present time, the data do not extend above 10 MeV.
eye and skin are not exceeded (Jahr et al., 1985).
Skin exposure is therefore of no practical concern for Electrons. Skin dose and personal
radiological protection against neutrons because of dose equivalent
the penetrating nature of the radiation and conver-
sion coefficients for directional dose equivalent for (346) Given the nature of electron interactions
neutrons are not given in this report. with matter, calculations of personal dose equivalent
in the human trunk, Hp(d), can be assumed to be
numerically equal to directional dose equivalent,
H'(0.07) in the ICRU sphere, or dose equivalent in
25 There are a few discrete energies in the neutron resonance
region where this general rule is violated (e.g., 1 MeV or 5.12 the ICRU slab, H p ,slabCO.07) (see Section 4.5). Figure
MeV), but the magnitude of the discrepancy is never significant 72 shows the ratio Hp ,skinIH'(0.07,00) [or Hp.skinl
(less than 10%). H p ,slab(0.07)] as a function of electron energy. 75
35
AP
f/\\
if :\
30 PA : b
LAT
25
ROT
ISO /' \\:,
/ \~
I \\
20
l!
~
/ \\\1
,,'/
-
:::::0,
~
15

10
//"
:.:::::~ - -----:.--:::::::-:.::::.:::::-:.-:.-:.~.~.~..
............
~ ,
\,\

'\ \
!.
5 ''""
'"
O~~~~~C;:'~'L'-~':"-~':"-~"':-:~:'-L~~-=~:'~~::--~~C-~.~.a·~··=\~~~··~·~J
10-8 10'7 10-6 lO's 10-4 10,3 10'2 10'1 10° 101

Neutron energy (MeV)

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Fig. 70. The ratio E / H p,testes for several irradiation geometries as a function of neutron energy.

Electrons. Effective dose and personal be concluded that, for photons and electrons, mea-
dose equivalent surement of the operational quantities for area
monitoring (ambient and directional dose equiva-
(347) For electron energies above 1.5 MeV, the
lent) will continue to provide a reasonable overesti-
contribution of the skin dose to the effective dose
mate (typically 20% or more) ofthe protection quan-
becomes negligible. Because of the increasing elec-
tron range, organs more deeply located in the human tities in all irradiation geometries.
body, such as the testes, red bone marrow, ovaries (349) This conclusion is also the case for neutrons
and stomach, are successively irradiated and make in most, but not all, irradiation geometries. There is
their contribution to E, as the electron energy in- a particularly important exception for the AP geom-
creases. Figure 34 shows a graph of effective dose for etry at low neutron energies (about 1 eV) where
AP geometry as a function of electron energy, A curve underestimates of the protection quantity by about
of B'(10) shown on the same graph shows that 25% can occur.
H p (10) overestimates E for electron energies above (350) Particular caution is required when dealing
about 2 MeV. At 10 MeV the overestimation is a little with radiations having energies above about 20 MeV,
more than a factor of2.5. because the operational quantities defined at a depth
of 10 mm in tissue may not provide sufficient overes-
timation of protection quantities.
5.3.4. Summary (351) For photons and electrons, measurements of
(348) Mter all the changes in definitions, specifica- the operational quantity for individual monitoring
tions, and physical databases are considered, it may (personal dose equivalent) should provide a good

35
AP
30 PA
LAT
ROT
25 ISO

00
a>
.e" 20
a>
..... ...
oS
r:.:
1C
t0

~
p,.
<ll
-
:::::c.
~
15

10
::;
~ 5
-
U

0
10-8 to,7 10-6 10's 10-4 10,3 10'2 10'\ 10° 10 1

Neutron energy (MeV)


76 Fig.71. The ratio E / Hp,thymus for several irradiation geometries as a function of neutron energy.
0.8

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Electron energy (MeV)
Fig. 72. The ratio of the skin dose, Hp,skin> to the directional dose equivalent, H'(O.07;OO), as a function of electron energy.

estimate of the effective dose in the geometries of (355) The analysis of the data presented in this
most interest for radiological protection (AP and report indicates that generally, but with a few excep-
ROT). However, care is required in other irradiation tions, the operational quantities continue to achieve
geometries (particularly the PAgeometry) ifunderes- their objective.
timation is to be avoided. This may be achieved by (356) There are some circumstances of irradiation
appropriately positioning personal monitors on the geometry or radiation energy in which the discrepan-
individual being monitored. cies between the two sets of quantities 26 are signifi-
(352) Measurement of the personal dose equiva- cant. These latter cases may be generally classified
lent will also potentially underestimate the effective into three groups: electrons and photons of low
dose at some energies for neutrons, even in the ROT energy (and therefore low penetrating power); inter-
geometry. However, under typical working condi- mediate-energy neutrons; and high-energy neutrons.
tions, where neutron energies are distributed over a (357) As a practical matter, radiations of low
broad spectrum of energies (e.g., fission neutrons or penetrating power rarely present practical problems
degraded fission spectra), a measurement of H p (10) of external exposure because they may usually be
is likely to be a reasonable measure of E (i.e., to reduced by modest shielding. Exposure to neutrons
provide an overestimate of25% or more). Knowledge generally occurs to broad energy spectra, in which
of the neutron spectrum in which measurements are case the operational quantities are generally ad-
to be made is always highly recommended if reliable equate. However, the high-energy radiations beyond
results are to be obtained. the scope of this report, such as are found in the
cabins of high-flying aircraft, need separate and
further study.
5.4. General Conclusions
(358) It therefore appears that the operational
(353) A major concern of this Section has been to quantities provide a satisfactory basis for most mea-
consider whether the operational quantities recom- surements for radiological protection against exter-
mended by IeRU, in the light of the new recommen- nal radiations. In those cases where this is not so,
dations in ICRP Publication 60, still achieve their the data provided in this report provide a basis for
objective in providing measurable quantities that designing special measurement programmes, prop-
adequately represent the protection quantities. erly interpreting their results and relating them to
(354) The operational quantities as originally speci- the protection quantities.
fied in 1985 were designed to satisfy the require- Acknowledgements - Some unpublished material
ments of ICRP Publication 26 and, with the excep- was made available to the Task Group during its
tion of the revision in the Q(L )-L relationship preparation of this Report and prior to publication.
recommended in Publication 60, remain essentially
unchanged. It is of great practical interest, therefore,
to understand their performance in the changed 26 That is, between the protection and the operational quanti-
conditions following release of Publication 60. ties.

77
ANNEXES
Introduction

These annexes contain figures (Annex 1) and should be remembered that they have been derived
tables (Annex 2) which support the text of Section 4. from idealised representations of the energy and
NOTE. The data in these annexes are presented orientation ofthe radiation fields and from idealised
with a high precision to help in making comparisons anthropomorphic computational models.
and to provide consistency in metrology. However, it

Contents
Annex 1 Figures Page
Photon data

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Fig. A. 1. Bladder absorbed dose per unit air kerma free-in-air 81
Fig.A.2. Bone (red marrow) absorbed dose per unit air kerma free-in-air 81
Fig. A.3. Bone (surface) absorbed dose per unit air kerma free-in-air 82
Fig.A.4. Breast (female) absorbed dose per unit air kerma free-in- a ir 82
Fig.A.5. Colon absorbed dose per unit air kerma free-in-air 83
Fig.A.6. Gonads, female (ovaries) absorbed dose per unit air kerma free-in-air 83
Fig.A.7. Gonads, male (testes) absorbed dose per unit air kerma free-in-air 84
Fig.A.8. Gonads absorbed dose (mean of ovaries and testes) per unit a ir kerma free-in- a ir 84
Fig. A.9. Liver absorbed dose per unit air kerma free-in-air 85
Fig. A. 10. Lung absorbed dose per unit air kerma free-in-air 85
Fig. A.H. Oesophagus absorbed dose per unit air k erma free-in-air 86
Fig.A.12. Remainder absorbed dose per unit air kerma free-in-air 86
Fig.A.13. Skin absorbed dose per unit air kerma free-in-air 87
Fig. A.14. Stomach absorbed dose per unit air kerma free-in-air 87
Fig.A.15. Thyroid absorbed dose per unit air kerma free-in-air 88
Fig.A.16. Effective dose per unit air kerma free-in-air 88
Fig.A.17. Eye lens absorbed dose per unit air kerma free-in-air 89
Fig.A.18. Thymus absorbed dose per unit air kerma free-in-air 89
Fig.A.19. Uterus absorbed dose per unit air kerma free-in-air 90
Neutron data
Fig.A.20. Bladder absorbed dose per unit neutron fluence 90
Fig. A.21. Bone (red marrow) absorbed dose per unit neutron f1uence 91
Fig.A.22. Bone (surface) absorbed dose per unit neutron fluence 91
Fig.A.23. Breast (female) absorbed dose per unit neutron fluence 91
Fig.A.24. Colon absorbed dose per unit neutron fluence 92
Fig.A.25. Gonads, female (ovaries) absorbed dose per unit neutron fluence 92
Fig.A.26. Gonads, male (testes) absorbed dose per unit neutron fluence 92
Fig. A.27. Gonads (mean of ovaries and testes) absorbed dose per unit neutron fluence 93
Fig. A.28. Liver absorbed dose per unit neutron fluence 93
Fig.A.29. Lung absorbed dose per unit neutron fluence 93
Fig.A.30. Oesophagus absorbed dose per unit neutron fluence 94
Fig.A.31. Remainder absorbed dose per unit neutron f1uence 94
Fig. A.32. Skin absorbed dose per unit neutron fluence 94
Fig. A.33. Stomach absorbed dose per unit neutron fluence 95
Fig. A.34. Thyroid absorbed dose per unit neutron f1uence 95
Fig. A.35. Effective dose per unit neutron fluence 95
Comparative neutron data
Fig. A.36. Evaluated and original data for the mean absorbed dose to bone marrow (males)
in PA geometry 96
Fig. A.37. Evaluated and original data for the mean absorbed dose to the colon (male) in AP
geometry 96
Fig. A.38. Evaluated and original data for the mean absorbed dose to the colon (male) in
RLAT geometry 96
Fig. A.39. Evaluated and original data for the mean a bsorbed dose to the colon (female) in
RLAT geometry 97
Fig. A.40. Evaluated and original data for the mean absorbed dose to the colon (male) in
LLAT geometry 97
Fig. A.41. Evaluated and original data for the mean absorbed dose to the colon (female) in
78 LLAT geometry 97
Annex 1
Contents
Figures Page
...'"
Q)

So
Fig. A.42. Evaluated and original data for the mean absorbed dose to the gonads (female, iZ
ovaries) inAP geometry 98 ....
:><
Fig.A.43. Evaluated and original data for the mean absorbed dose to the gonads (male, Q)
~
testes) in ROT geometry 98 ..;j
Fig. A. 44. Evaluated and original data for the mean absorbed dose to the liver (male) in PA
geometry 98
Fig.A.45. Evaluated and original data for the mean absorbed dose to the liver (male) in
RLAT geometry 99
Fig.A.46. Evaluated and original data for the mean absorbed dose to the liver (female) in
RLAT geometry 99
Fig.A.47. Evaluated and original data for the mean absorbed dose to the liver (male) in
LLAT geometry 99
Fig.A.48. Evaluated and original data for the mean absorbed dose to the liver (female) in
LLAT geometry 100
Fig.A.49. Evaluated and original data for the mean absorbed dose to the lungs (female) in
APgeometry 100
Fig.A.50. Evaluated and original data for the mean absorbed dose to the remainder (male)

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


in PA geometry 100
Fig.A.51. Evaluated and original data for the mean absorbed dose to the stomach (male) in
RLAT geometry 101
Fig.A.52. Evaluated and original data for the mean absorbed dose to the stomach (female)
in RLAT geometry 101
Fig.A.53. Evaluated and original data for the mean absorbed dose to the stomach (male) in
LLAT geometry 101
Fig.A.54. Evaluated and original data for the mean absorbed dose to the stomach (female)
in LLAT geometry 102
Fig. A.55. Evaluated and original data for the mean absorbed dose to the thyroid (female) in
PAgeometry 102

Comparative data on effective dose from neutrons


Fig.A.56. Evaluated and original data for the effective dose in AP geometry 102
Fig.A.57. Evaluated and original data for the effective dose in PAgeometry 103
Fig.A.58. Evaluated and original data for the effective dose in RLAT geometry 103
Fig.A.59. Evaluated and original data for the effective dose in LLAT geometry 103
Fig.A.60. Evaluated and original data for the effective dose in ROT geometry 104
Fig. A.6l. Evaluated and original data for the effective dose in ISO geometry 104

Annex 2 Tables
Photon data
TableA.l. Conversion coefficients for air kerma per unit fluence of monoenergetic photons 105
TableA.2. Bladder absorbed dose per unit air kerma 105
TableA.3. Bone (red marrow) absorbed dose per unit air kerma 105
TableA.4. Bone (surface) absorbed dose per unit air kerma 105
TableA.5. Breast absorbed dose per unit air kerma 106
TableA.6. Colon absorbed dose per unit air kerma 106
TableA.7. Gonads, female (ovaries) absorbed dose per unit air kerma 106
TableA.8. Gonads, male (testes) absorbed dose per unit air kerma 106
TableA.9. Gonads absorbed dose (average of male and female) per unit air kerma 107
TableA.10. Liver absorbed dose per unit air kerma 107
TableA.U. Lung absorbed dose per unit air kerma 107
TableA.12. Oesophagus absorbed dose per unit air kerma 107
TableA.13. Remainder absorbed dose per unit air kerma 108
TableA.14. Skin absorbed dose per unit air kerma 108
TableA.15. Stomach absorbed dose per unit air kerma 108 <fJ
0>
TableA.16. Thyroid absorbed dose per unit air kerma 108 ....
0>

TableA.17. Effective dose per unit air kerma 109 ~


lD
TableA.18. Eye lens absorbed dose per unit air kerma 109
TableA.19. Thymus absorbed dose per unit air kerma 109
~
...
0
p.
TableA.20. Uterus absorbed dose per unit air kerma 109 ~
Q)

TableA.2l. Conversion coefficients for ambient dose equivalent and directional dose equiva- ~
lent from photon fluence and air kerma 110 ~
TableA.22. Conversion coefficients for directional dose equivalent, H'(10,OO), from air kerma 8
and angular dependence factors 110
TableA.23. Conversion coefficient for directional dose equivalent, H'(O,07,OO), from air kerma
and angular dependence factors 110
TableA.24. Conversion coefficient for H p(10) in an ICRU slab from air kerma and angular-
dependence factors 110 79
I': Contents
0
:;l Annex 2 Tables Page
<d
:.a<d TableA.25. Conversion coefficients for H p(0.07) in an ICRU slab from air kerma and angular-
c.:: dependence factors up to 75° (Grosswendt, 1991) 111
<ii Neutron data
E TableA.26. Bladder absorbed dose per unit neutron fluence 111
~
>< TableA.27. Bone (red marrow) absorbed dose per unit neutron fluence 112
ril
....,
en TableA.28. Bone (surface) absorbed dose per unit neutron fluence 112
.;I': TableA.29. Breast (female) absorbed dose per unit neutron fluence 113
TableA.30. Colon absorbed dose per unit neutron fluence 113
~ TableA.31. Gonads, female (ovaries) absorbed dose per unit neutron fluence 114
I':
0
'.;3 TableA.32. Gonads, male (testes) absorbed dose per unit neutron fluence 114
t.>
TableA.33. Gonads (mean of ovaries and testes) absorbed dose per unit neutron fluence 115
~
...0 TableA.34. Liver absorbed dose per unit neutron fluence 115
Po. TableA.35. Lung absorbed dose per unit neutron fluence 116
<iit.> TableA.36. Oesophagus absorbed dose per unit neutron fluence 116
'6h TableA.37. Remainder absorbed dose per unit neutron fluence 117
0
'0 TableA.38. Skin absorbed dose per unit neutron fluence 117
;a TableA.39. Stomach absorbed dose per unit neutron fluence 118
~ TableAAO. Thyroid absorbed dose per unit neutron fluence 118

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.5 TableA.41. Effective dose per unit neutron fluence 119
Q)
en TableA.42. Ambient and personal dose equivalent per unit neutron fluence, H*(IO)I<P and
;::l
... H p ,slab(IO,a)l<P 119
r£ Electron data
.r'5
I':
Q)
TableA.43. Conversion coefficients for organ absorbed dose and effective dose from electron
' <) fluence 120
!:S
Q)
TableA.44. Reference conversion coefficients for directional dose equivalents from electron
0 fluence 120
U
I': TableA.45. Reference values of the angular factor at a depth of 0.07 mm 120
0
'iii TableA.46. Reference values of the angular factor at a depth of 3 mm 121
...
Q) TableA.47. Reference values of the angular factor at a depth of 10 mm 121
>
I':
0
U

80
ANNEX 1. FIGURES
2.0 AP
PA
LAT
ROT
ISO

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0 . 10 1.00 10.00
Photon energy (MeV)
Fig.A.I. Bladder absorbed dose per unit air kerma free-in-air.

1.5
AP
PA
LAT
ROT
ISO
'. '.
" . ".
........ ... .... ........... .. .. .... .
........ ~.' ......

,':
. / -......... ~..-;:::" .....
: I/' ---- _ _ _ -:: ..........
...
G)
: :'/~-----------
c:>. : I VI
~ 0.5
: : I
"0 :i I
1l :
: • I
: ,
.' ,
~ ,
:'

..
.t:>
: :
.: I,

~
;' :' I
..../,~
.... ..
o 0.0u-__~~~~~~u-__~__~~~~~__~__~~~~~
0.01 0.10 1.00 10.00
Photon energy (MeV)
Fig.A.2. Bone (red marrow) absorbed dose per unit air kerma free-in-air. 81
::: 3.0
.S
..., AP
e<S
;a PA
~
e<S
S !.AT
ROT
OJ
::: 5
'-'
2.5
ISO
...,'"
(1) ~.
>: "1:-
r:tl
..., Cl
2.0
00
::: '"..,E
"a
<:::
~
..
'(i!

·s 1.5
.S
...,
u
...,
(1) ....,
::s
0
'"
0..
..,c:>.
OJu
'"
0
"0
1.0 ...................................
'M
"0 ..,
0 of
'0 0
;a .0 '" 0.5
~
e<S
'"c
'"

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.S e!l
(1) 0
00
::s 0 . 0u-~~ __~~~~u-__~__~~~~~__~__~~~~~
0.01 0.10 1.00 10.00
'"
<Sl
Photon enerlrY (MeV)
..,
00
::: Fig.A.3 . Bone (surface) absorbed dose per unit air kerma free-in-air.
.u~
!E(1)
0
U
:::
.S
00
'"
(1)
;>
:::0
u

2.0
-. AP
>. PA
~ !.AT
ROT
0
'-'
~ .. ISO
"1:- 1.5
Cl

~
.,'"
E
·iii
·s::s 1.0
00
(j)
(j)
.,...
.-<
.,.:
..,c:>.
l!') 0'"
"0
1::0
c:>.
.,
"0

(1) of 0.5
0
~
::> '"co
.0

~ C
U co
...... e!l
0
.'
0. 10 1.00 10.00
Photon energy (MeV)
82 Fig. A.4. Breast (female ) absorbed dose per unit air kerma free-in-air.
1.5

· ....... .
'.
/./.......... '" .........................:.:.:::::.:.:::::.:.:::::::.:.-=
:::t .......... - ... _ ... _ ... .- ... -... ~ --::~::::.~ . -.
" ...-;";:.--.-
j ---.
......... ---- , - :'..... - ,..
: / ""'-----:':. ........ .
! / ,. -'-
- - - - - - -_.-.-'
- - - _.-'
I: / 1,./' '-._._ . - '
: / I.' AP
1/ II1/

PA
LLAT
/tt!

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RLAT
:·i':i i I ROT
.·71
o.ou-____~~·~/~~~~wu~__~__~~~-L~~~ __~___L~~_L~~
ISO

0 .01 0.10 1.00 10.00


Photon energy (MeV)
Fig. A.5. Colon absorbed dose per unit air kerma free-in- air.

1.5n---~r-~~~~MI----~-T-T-.~~r----.--~~-Arp~rn

PA
LAT
ROT
ISO

:::
... .. ................. :~:::: ;.:.......--:::.~::
_... _... - ... -
!/
Ii ...- . . . .
;':' / .........
........ ..

_-_.----
- ...

-- --
11/
I;' / ,. - - - - - - - ---
If / /
1.'/ 1
'. I
.l /I
.:; I
,.'l,.'
O.Ow-____~~·~/~~~~~L__ _ _ _~_ _~~~~~~_ _ _ _~_ _~~~~~~u
0.01 0 . 10 1.00 10.00
Photon energy (MeV)
Fig.A.6. Gonads, female (ovaries) absorbed dose per unit air kerma fr ee-in-air. 83
~ 2.0
.S
+'
AP
PA
;.s""
""
p:: ~ LAT
ROT
til
e ~ ISO

.2l~
~ .. 1.5
>il
+'
~ ..
rJl
~
'0; ~
5
~ ....
~
'cu 1.0
0
:;:l '2:s
<.>
<I)
+' tc:l.
0
ct Q)
II>
0
til<.> "C

'6'.0
0
'0
"C

-e
Q)

0
0.5
--
;.s ~
II>

""
p:: ..e!l
c

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.S
<I)
rJl
0
:s
.... 0.10 1.00 10.00
<£ Photon energy (MeV)
rJl
+'
~ Fig.A.7. Gonads, male (testes) absorbed dose per unit air kerma free-in-air.
.<.>~
IE
<I)
0
u
~
.SrJl
....
<I)
>
~
0
u

2.0 AP
PA

~
';>.,
LAT
ROT
0 ISO
'-'
~ .. 1.5
~..§
Q)
~
....
'cu 1.0
·s:s
.(-:.~:""""''''''''''-':':':':::'''~::':::'.'::::':':::':':'''''''::'':-:~;?:
00
O"l
....
----- ---
O"l
...... Q)

t-"
10
c:l.
Q)
II>
:.:
/:/
",- --
..........
~----
0
t0 "C .:/
Po.
<I)
p::
"C
Q)

-e0
0.5 .II:" ----
~
Ii.:" .-
~
II>
./'.: "
p::
u
...... c.
e!l
i : ""
./ :
,: /"
0 0.0 ..-'" .... :../
0.01 0.10 1.00 10.00
Photon energy (MeV)
84 Fig. A.S. Gonads absorbed dose (mean of ovaries and testes) per unit air kerma free-in-air.
1.5
AP
PA

~
8-
LLAT
RLAT
ROT
'1<," ISO
~ .. 1.0
.,
E
.;c
...' OJ
.t::
c
:l
.,...
.,
Q.

... ...
VI
0 (,.5
-0
-0.,
of

.......
0
VI

--- --
.D

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C
CIl
0
0.0
0.01 0 . 10 1.00 10.00
Pholon ener,y (MeV)
Fig.A.9. Liver absorbed dose per unit air kerma free-in- air.

1.5

~
'1<."
~.. .......... ... .........

E
1.0
". __
.,
, '- .
_- .-... - "'-'"
... ... -
- - :----=
--
--
.;c .. --. . . . ... ...
... . . ,-.......... ....-""-
...
'OJ
·s .: ,:/ '- ""'------
....,:l : : /
.,.,
Q. j il ,'---------
0 0 .5 :: , !I I '
-0
.,
-0 / .:/1
of0 i ! I,' AP
~
VI
,.: il I PA
.C

e!l
.:' :/,'
....1/ I
LAT
ROT
0
0.0
....~.... ' ISO

0.01 0.10 1.00 10.00


Pholon energy (MeV)
Fig. A.IO. Lung absorbed dose per unit air kerma free-in-air. 85
1.2

............
S
e
'-'
1.0 ' .....
" ............. .....
~"
~.. O.B _
.. - . . . ... .,., ... "
E
"
.:.:
...
'iii
0.6
'2;:s
...
"
Q,

"
~
"0
0.4
"0

"
of
AP
0 PA
~
'" 0.2 LLAT
c. RLAT

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e!l ROT
0 ISO

0.10 1.00 10.00


Photon energy (MeV)
Fig. A.ll. Oesophagus absorbed dose per unit air kerma free-in- air.

1.2

S
e
'-'
1.0

~"
~.. O.B
E
..."
.:.:
'iii
'2;:s 0.6
co ...
0>
0>
.... "
Q,

t-"
...,
LC
"'"0
"0 0.4
...
0
"0
Q, "0
of AP
& '"
PA
::> ~ LLAT
p::
Co)
......
c..
f!l
0.2
RLAT
ROT
0 ISO
0.0
0.01 0 .10 1.00 10.00
Photon energy (MeV)
86 Fig. A.12. Remainder absorbed dose per unit air kerma free-in-air.
S
&
..
'-'
~

~
1.0
:/~··-··· .......... ---.
I' / - __ __
.. _0"-··'-·"-"
-":;:-_
. "- .... _ ... _0. .....___

-------~--
--- ------
..
E
0.6
:/ ,
.
//,----------- --
..
~

.;
II '
'2
::s
0.6 /1 "
:/ I

8. .Ii "
~
/1'
.g 0.4 :1 "
.~ ,
i
1l
.. 0.2 /1
Ii,'
·'0' AP
PA
LAT
~

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I
ROT
o ISO

0 . 10 1.00 10.00
Photon energy (MeV)
Fig.A,13. Skin absorbed dose per unit air kerma free-in-air.

2.0
AP
PA
LLAT
RLAT
ROT
ISO

/::. .:::. ..........


II
I.~I
..'
. ..... '0, " - .....-=-'7..-:' . :-:: _.-:._.-.:.::';"~' ~.'2
. ........... .. .. .. ........ __
::-:: ::-.:::::-.:::
l" .0/ - -.... ___ --
II ----
f/
I,:'
I I:
il':
,;:
j ...
~ . .... ".
0 .0u-__~~~~~~~____~~~~~~____~~~~~~~
0.01 0 . 10 1.00 10.00
Photon energy (MeV)
Fig. A,14. Stomach absorbed dose per unit air kerma free-in-air. 87
I=i
0 2.0
~
til
AP
PA
;.a
til
p::
S
">. LAT
(:>
........
ROT
til ISO
e '><,"
1.5
~
Q)

t<
..., OS
"''""
.S
E
~
til
bIl ...
' 01
<I=i .~
.S 1.0
..., .,...::s
CJ
...,0
Q)
.,""
'"
Il.. '"0
"0
tilCJ
1l
'5h of D.l -
.Q ~
0
;.a .&>
OS
c<J
p:: c::
OS
...CO

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.S 0
Q)

::s'"
'"
C£ 0.10 1.00 10.00
...,'" Photon energy (MeV)
I=i
.CJ~ Fig. A.15. Thyroid absorbed dose per unit air kerma free-in-air.
IEQ)
0
U
I=i
.,
.S
'"
Q)
>
I=i
0
U

1.5

~
~
~

-
,,<"
f.:<
01
S
1.0
.! .-: - ;. . <:::.....,,_.. _". _"._ ...:':"':"-'...., ~::~.~_.-,r...-
...... _0. .... .. .. .. ... . ... . .. . .. . ..... ::.:-....::;..:....."'# __ ... ,..r..
.,'"
.:.:
--- - -
/ ,- -... . . . . . -- -:: -:::*,.;:.::...,..
00
O"l
-=
.;'"
: / - -::. -::'"'..........
;7!/ ///"_.-._._._._._.-
/'" - - - - - - - - -.:.-.-'
O"l
..... ·C

::/ ,,,
t-"

.,'"~
LO 0.5
"t0
'"0 if: 1/ AP
""
Q)
p:: ~
., : : II
il'; PA
~
p::

-
U -
.::
~
~
CJ
.,'1;
;.
:"f
~.
LLAT
RLAT
ROT
//..'/' ISO
~.'
0.0
0.01 0. 10 1.00 10.00
Photon energy (MeV)
88 Fig.A.16. Effective dose per unit air kerma free-in-air.
2.0 AP
PA
LAT
ROT
ISO

.. '

.. .. '
'
.. ,

.. '

.. ' .. '
.... .....

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0.10 1.00 10.00
Photon energy (MeV)
Fig.A.l7. Eye lens absorbed dose per unit air kerrna free-in-air.

2.0 AP
PA
LAT
ROT
ISO

:/
.... -. ....... ,o-
j - - "'-"'-"'-"'=':;~'~~.:
/// -------:--
.... ....
/1:'1 - - -
I~' :":-: '::::"" " " """ """"
....

il ' ....
'j ,,'
;' I:'
:/ ,,'
~ 1/
O.Ou-__~e·~·~-~~~··~·~~~~L___~~~~~~~~____~__~_J_J~~~J
0.01 0.10 1.00 10.00
Photon energy (MeV)
Fig. A.l8. Thymus absorbed dose per unit air kenna free-in-air. 89
~
0
:;:l
1.5 AP
;e
oj PA
LAT
~
oj
6'"' ROT
0;
e S
'-'
ISO
OJ
+' l<'"
~
~
~
+'
00 oS 1.0
~
E
., ........................................
'0;
~
~
~
...
'0; __ - ::~::::::~:'.­

... .... -.... - .... ---...-::::::-- - . ---'


0
..;:: os Ii ,,- ~"'~-
'"
OJ
+'
;:I
.,p..... i,' / - -- __ __ ....- ----I',.
...0
p.., ., ::i / -------
II>
0.5
j'f ---
n ," -----
0
0; "0
'"
'So .,
"0
0
'0 -e !f '
;e ~
~
~
oj
c:: if "
II ,'

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oS
.S /
OJ 0
e!l
.// ,
00
;:I
o.ou-___~~~~~~--~~~~~~~--~~~~~~
... 0.01 0.10 1.00 10.00
<£ Photon energy (MeV)
00
+'
~
OJ
Fig.A.I9. Uterus absorbed dose per unit air kerma free-in-air.
'u
!EOJ
0
<:)
~
.S
...
00
OJ
>
~
0
<:)

102 AP
PA
5 LAT
ROT
ISO
....'"' 10\
00
0>
e...
,...,
0>
.... 5
r.: ~
It:>
p..
'-'
1::0 €; 10°
~ ""
OJ "1-
S, 5
~
~
<:)
......
10'\ I...L...............~.....................L..~~.......JL................-:-"'....J..-:-"'"........~...I....:'........""-:-~~
10.9 10-8 10.7 10'" 10.5 10-4 10.3 10.2 10.1 10° 101 102

Neutron energy (MeV)


90 Fig. A.20. Bladder absorbed dose per unit neutron fluence.
101 AP
PA
5 LAT
ROT
ISO
....,-..
E 101
U
.... 5
~

--
~
Co

~ 10°

--
~
5

10.1 1..L.......................L...........L..........L.........Lo...........I....,...........~.....L..~""'-:........o/...::'........."'-:'-l
10.9 10-3 10.7 10-6 10's 10-4 10.3 10.2 10.1 10° 101 102

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Neutron energy (MeV)
Fig.A.21. Bone (red marrow) absorbed dose per unit neutron fluence.

AP
PA
LAT
ROT
ISO

10.1 ...............................o/...::'..........t..............L.............~....................L...........................L.............L..........L....J
10.9 10-3 10.7 10-6 10's 10-4 10.3 10.2 10.1 10° 101 101
Neutron energy (MeV)
Fig. A.22. Bone (surface) absorbed dose per unit neutron fluence.

IOZ AP
PA
5 LAT
ROT
ISO

10.1 l...L................,..........L...........L.........~........~....................L..:"""'................o/...::'........t...............L....J
10.9 10-3 10.7 10-6 10's 10-4 10.3 10.1 10.1 10° 101 102
Neutron energy (MeV)
Fig. A.23. Breast (female) absorbed dose per unit neutron fluence. 91
101 AP
PA
5 R-LAT
L-LAT
ROT
.....-. ISO
e... 10·
.... 5
t.!l
c:r.
'-'
I§;'
10°
~
-- 5

Neutron energy (MeV)


Fig. A.24. Colon absorbed dose per unit neutron fiuence .

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101 AP ..... .,
PA
5 LAT //
ROT ,i/
.. I
ISO fl,'
.....-. /,

...e 10· /1,'


.... 5
Ij/
! ,
Co'

-------=-=-=-=~~=:fj
c:r.
'-'
I§;'
~ 10°
----------------
/~-----------
'-'
5
-
------ " /
/

10·. 1..L.......................................L................-w.o.........~..1....:'........~......._:_"~::_'"'":'........"'_:'_"
10-' 10-8 10.1 10-4 10-s 10-4 10-3 10-1 10-1 10° 101 101
Neutron energy (MeV)
Fig.A.25. Gonads, female (ovaries) absorbed dose per unit neutron fiuence.

101 AP
PA
5 LAT
ROT
ISO
.....-. 101
e
.......
00
m
m
...... 5
t.!l
t--"
It:l
c:r.
'-'
t: I§;'
~
8-
~ ;;r
'-"'
10°
5
~
Q
......
10-1 ..................................................................~--........""'-:........""'""":'...................."'-:'......."'--:-'......."'-:'-'
10-9 10-8 10-' 10-4 10-s 10-4 10-3 10-1 10-1 10° 101 101
Neutron energy (MeV)
92 Fig.A.26. Gonads, male (testes) absorbed dose per unit neutron fiuence.
101 AP
PA ,i/';
5 LAT
ROT ,IV
ISO /1,1
j!/
...
,-.
101
.f; I"l
5
....u 5 .If:
c.!l /1-/ :
.• I
g,
.....,..::".'!:::7::::::.::.::::~.:::.:~.::~:.::::~.=:.:::::::~~T
.. / - - -
/
'-'

€ 10° - - -- - - .,,'
=-.;. . .~-;~;:~...... ......
~
'-'
5
~~
-_ ... -----
-----------------_ ... -....,/
~~

.-------'
10.1 .......:-"""""-:~""-::~"'-;.........."-:-........~...........l..:'-'......J.-:-'".......~.....I....::'-""'~.........~
10.9 10-3 10.7 10-' 10.5 10-4 10.3 10.1 10.1 10° 101 101

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


Neutron energy (MeV)
Fig. A.27. Gonads (mean of ovaries and testes) absorbed dose per unit neutron fiuence.

101 AP
PA
5 R·LAT
L-LAT
ROT
.....-.. ISO
5U 101
.... 5
c.!l
c.
'-'

~
'-'
10°
5

Neutron energy (MeV)


Fig. A.28. Liver absorbed dose per unit neutron fiuence.

101 AP
PA
5 LAT
ROT
ISO
.....-..
5U 101
.... 5
~
g,
.......

10°
~
'-' 5

10. 1 .........................................,..................................,............................................,.................,........""-:-...............,............"'-'-J
10.9 10-3 10.7 10-' 10.5 10-4 10.3 10.1 10. 1 10° 101 101
Neutron energy (MeV)
Fig. A.29. Lung absorbed dose per unit neutron fiuence. 93
AP
PA
5 LAT
ROT
ISO

10··~~~~~~~~~~--~~~~~~~~~~~~~
10.9 10" 10-7 10-4 10's 10-4 10-l 10.2 10-· 10° 10· 102

Neutron energy (MeV)

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


Fig. A.30. Oesophagus absorbed dose per unit neutron fiuence.

102 AP
PA
5 LAT
ROT
ISO
..........E 10·
\,j

~ 5
c.!)
Co
'-'
~- ........ --.--.--------
~
;;r
'-'
10°
5
---------

10'· ..............""-............................................................................-!'-'"""""-......."'-:'...................~
10.9 10" 10-7 10-4 10's 10-4 10·l 10-2 10-· 10° 10· 102
Neutron energy (MeV)
Fig.A.3!. Remainder absorbed dose per unit neutron fiuence.

102 AP
PA
5 LAT
ROT
ISO
....,.....
10· .,fI'
OCJ E (if'
~ \,j

....
~
~
c.!)
5 0'
r-: Co -A/
It:)

~
0
p.
Q)
~
'-'

'1- 10°
__-----::====-----::
_-._____- _. ..
... ... ... ...
._______ ==-=:.-7-==-::.---=_..:::_=-~,'"
... ... ... ,- ",/ /1/
~/

~
;:J
S. 5
~
Co.)
......
10'· ......."!"""'............~~............""'-:...................""-:".....-""-:".....-............"-:'-........"-:'-......'-:'-'
10.9 10" 10.7 10"' lO's 10-4 10.3 10-2 10-· 10° 10' 102
Neutron energy (MeV)
94 Fig.A.32. Skin absorbed dose per unit neutron fiuence.
1~ AP
PA
5 R-LAT
L-LAT
ROT
.....-. ISO
ev 10 1
;...
~ 5
Q,
'-'
I§'
~
'-'
10°
5

Neutron energy (MeV)

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


Fig.A.33. Stomach absorbed dose per unit neutron fluence.

101 AP
PA
5 LAT
ROT
ISO

.....-. 101
ev 5
;...
~
Q,
'-'
I§' 10°

~
'-'
5

10,1 l-L............L...~.L...~.L............L.............~.....L..............L............L..........L...~.L............I.-..J
10,9 10-8 10'7 10-<1 10,5 10~ 10,3 10,1 10'1 10° 101 102

Neutron energy (MeV)


Fig. A.34. Thyroid absorbed dose per unit neutron fluence.

103
AP
5 PA
R-LAT
L-LAT
ROT
1~ ISO
............
E 5
0
>
rIl
0-
'-'
~ 10
1

~
'-' 5

Neutron energy (MeV)


Fig. A.35. Effective dose per unit neutron fluence. 95
lot - - - Evaluation
GSF-I
5 " GSF-2
University of Texas
° JAERl
AGH&KFA
PNL
PTa

10-\ 1..L~w.L~.....L~.....L.........L.............L..~..L....~.a......~.a........~L....""""L.............t-...l

l~ l~ 1~ 1~ l~ l~ l~ l~ l~ l~ 1~ lot
Neutron energy (MeV)
Fig. A.36. Evaluat ed and original data for the mea n absorbed dose to bone marrow (male) in PAgeometry_

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


lot - - - Evaluation
9 GSF-I
5 GSF-2
" University of Texas

.e
-.
Col
10\
JAERl
°0 AGH&KFA
PNL
• PTa
~ 5
C,,!) 0

......
Q.

~ 10·
~
...... 5

10-\
10-' lO-s 10-7 10-6 10-s 10" 10-3 10-1 10-\ 10° 10\ lot
Neutron energy (MeV)
Fig.A.37. Evaluated and original data for the mean absorbed dose to the colon (male) inAP geometry_

lot
5 - - - Evaluation
o
GSF-I
" GSF-2
University of Texas
10\ ° JAERI
....-. o AGH&KFA
e
Col
5 PNL
~
C,,!)
Q.
'-'
10°
~ o 0 0 000 o 0 0 o 0 CD 0 ooov
000
• • • • • ., Ii °0
~ 5 0

'-' .. ° .. 0
• 0 .. o.<t!/' 0°/'

10-\
5UL~~~~~~~~~~~-L~~~~~~~
10-' 10-· 10-' 10-6 10-s 10" 10-3 10- 1 10-\ 10· 10\ lot
Neutron energy (MeV)
96 Fig. A.38. Evaluated and original data for the mean absorbed dose to the colon (male) in RLAT geometry_
to' - - - Evaluation
GSF-I
5 " GSF-2
University of Texas
o JAERI
AGH&KFA

0 0 0

5~~~~~~~~~~~~~~~~~~~~~~

I~ t~ I~ I~ I~ I~ I~ I~ I~ I~ 1~ to'
Neutron energy (MeV)

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


Fig.A.39. Evaluated and original data for the mean absorbed dose to the colon (female) in RLAT geometry.

10' Evaluation
GSF-2
5 " University of Texas
0 AGH& KFA
....-.
E 10'
(oJ
>.
(,.') 5
!:.
'-'

€ 66 b A

--
~
'-'
10' " 000
" "
" "OOcP° oOO

I 0·' .......:'"'""'""'-........."""-............L-.......""'-..........L.............................L............L...~L.............L.............L....I
10-9 10-8 10-7 10-6 10-5 I O~ lO-l 10-' 10-' 10° 10' 10'
Neutron energy (MeV)
Fig. A.40. Evaluated and original data for the mean absorbed dose to the colon (male) in LLAT geometry_

10' Evaluation
GSF-2
5 " University of Texas
AGH& KFA
PNL
....-.
S 10'
(oJ
>. 5
(,.')
!:.
'-' • ~~ • .p. • 0

€ " • " 0

-- " o" o
QOq,oooo
tOO 0 0 0 0 o 0 0

~
'-' 5

10-' l..L........wL.........w.L...........................................L..........................L.........L.......................................'-'-1
10-' 10-8 10-7 10-' 10-5 10~ 10-l 10-' 10-' 10' 10' 10'
Neutron energy (MeV)
Fig. A.41. Evaluated and original data for the mean absorbed dose to the colon (female) in LLAT geometry. 97
10' - - - Evaluation
GSF-I
5 GSF-2
" University of Texas

--
M
E
(,/ 10'
0 JAERI
AGH & KFA
PNL
>. PTS
5
""~
Co
'-'
~
o. b x x x )(

~ 10'
S- 5
~

10-'
10-9 10-" 10-' 10-" 10-5 10-' 1O- 10-1 10-' 10· 10' 10'
'
Neutron energy (MeV)
Fig. AA2. Evaluated and original data for the mean absorbed dose to the gonads (female, ovaries) in AP geometry.

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


10' - - - Evaluation
GSF-I
5 GSF-2
" University of Texas
0 JAERI

--
M
E
(,/
10'
x
AGH&KFA
PNL
PTB
>. 5

""
Co
'-' 0

~ 10' 0

~
~ 5
'-'

10·' l..L.............L.............L.u.u....L..........J...-...........L.............L...-'""'.l.............L.............."--'-~"--'-.......~
10·· 10·· 10·' 10.6 10. 5 10·' 10·l 10.1 10-' 10· 10' to'
Neutron energy (MeV)
Fig. A.43. Evaluated and original data for the mean absorbed dose to the gonads (male, testes) in ROT geometry.

10' - - - Evaluation
GSF-I
5 GSF-2
" University of Texas

OCJ
--
M
E
(,/
10'
0 JAERI
AGH& KFA
PNL
0>
>. PTS
....
0>

~
...,...
I.(.) '"
'-'

~
Co
5

• o· 0
0
0..
Q)
p:: ~
'-'
10'
~ 5
p::

-
C)

10·'~~~~~Lu~L.~~.w~~~~~~~~~~~~~L-U
10.9 10.8 10·' 10.6 10-' 10" 10·l 10-2 10·' 10· 10' 10'
Neutron energy (MeV)
98 Fig.A.44. Evaluated and original data for the mean absorbed dose to the liver (male) in PAgeometry.
1()l - - - Evaluation
GSF-I
5 6 GSF-2
~ University of Texas
c JAERI
N
.-.. AGH& KFA
E
CJ
10' PNL
;... 5
C

IS --
c.

~
10·
...... 5

I~ I~ 1~ 1~ 1~ 1~ 1~ 1~ I~ 1~ 1~ 1()l
Neutron energy (MeV)

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


Fig.A.45. Evaluated and original data for the mean absorbed dose to the liver (male) in RLAT geometry.

10' - - - Evaluation
GSF-\
5 6 GSF-2
University of Texas
N
....... c JAERI
E AGH& KFA
CJ 10'
;...
C 5
c.
......
IS
? 10·
5

10" L.L~....L~......L~.......~.......c......"""'L........""""L........~L........_L........_L...-~L....~~

1O'? 10'· 10" 10,6 10" 10" 10,l 10" 10" 10' 10' 1()l
Neutron energy (MeV)
Fig.A.46. Evaluated and original data for the mean absorbed dose to the liver (female) in RLAT geometry,

1()l~~~~~~~~~~~~~~~~~~~~
5 Evaluation
6 GSF-2
University of Texas
AGH&KFA
....... 10'
N
'S
CJ
5
;...
C
c.
'-' 10'
IS
? 5

10"
5~~~~~~~~~~~~~~~~~~~~~

1~ l~ l~ 1~ 1~ 1~ 1~ 1~ W4 1~ 1~ 1()l
Neutron energy (MeV)
Fig.A.47. Evaluated and original data for the mean absorbed dose to the liver (male) in LLAT geometry. 99
102
Evaluation
S
.. GSF·2
University of Texas
AGH& KFA
.....-. 10' PNL
E
Col
.... s
c.!I
--
c.
I§' 10·

--~ S

10"
S~~-L~~~~~~~~~~-L~-L~~~~~~

10" 10'· 10" 10" 10.5 10" 10') 10.2 10" 10' 10' 10>
Neutron energy (MeV)
Fig.A.48. Evaluated and original data for the mean absorbed dose to the liver (female) in LLAT geometry.

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


10> - - - Evaluation
GSF·l
S .. GSF·2
University of Texas
0 JAERI
0 AGH&KFA
10' PNL
x PTB
S
00 0

10" l..L~.....L~.....L ..........L..........L...........L.........L........................""",~L....~L......."""'L....J


10" 10'· 10" lit' 10" 10" 10-' 10.2 10" 10· 10' 10>
Neutron energy (MeV)
Fig. A.49. Evaluated and original data for the mean absorbed dose to the lungs (female) in AP geometry.

102 - - - Evaluation
GSF·l
S .. GSF·2
University of Texas
N
.-.. c JAERI
E AGH&KFA
00 Col 10' PNL
Ol
Ol .... PTB
M c.!I S
r.: c.
'-'
to
1:: €
0
A "1-
Q)
p::: l:::l
'-'
;:J S
p:::
u
....
10·'l..L~~~~~~~~~~~~~~~~~~~~~~~
1~ 1~ I~ I~ 1~ 1~ I~ 1~ I~ 1~ 1~ 10>
Neutron energy (MeV)
100 Fig. A.50. Evaluated and original data for the mean absorbed dose to the remainder (male) in PA geometry.
rJl
10' ...
QJ

5 --- Evaluation 6'n


GSF-l if:
A GSF-2 ...;
University of Texas >:
QJ

,.-. 10' 0 JAERI ~


N

eu
0 AGH&KFA
PNL
~
5

G
.e 10·

--c:r
"-'
5 000

/I
000

&
00
0 00

10"
s~~~~~~~~~~~~~~~~~~~~
2
9 10.
10'. 0 10" 10" 10" 10. 10" 10-' 10. 10' 10' 10'
Neutron energy (MeV)

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


Fig.A.51. Evaluated and original data for the mean absorbed dose to the stomach (male) in RLAT geometry.

10' - - - Evaluation
GSF-l
5 A GSF-2
University of Texas

N
--
E
y
10'
o
o
JAERI
AGH&KFA

5
G
c.
'-'

€ 10·

~
"-'
5

10"
S~~~~~~~~~~~-L~~~~~~~~~-u

1~ 1~ 1~ t~ 1~ 1~ 10-' 10-' 1~ 1~ 1~ 10'


Neutron energy (MeV)
Fig. A.52. Evaluated and original data for the mean absorbed dose to the stomach (female) in RLAT geometry.

10' Evaluation
A GSF-2
5 University of Texas
0 AGH&KFA

N
.-
E
y
10'
~ 5
to!)
'-'
c.
6. 1111 11
€ A
A A A A
00

;;r
'-'
10·
5 o
A

0
0
000
o 0 0 000 000 0 0 ell 0
0

10" ~~~-U~~~~~~~~~~~~~wL~~~~-U~~
10.9 10.0 lit' 10.6 10" 10" 10.3 10.1 10" 10' 10' 10'
Neutron energy (MeV)
Fig. A.53. Evaluated and original data for the mean absorbed dose to the stomach (male) in LLAT geometry. 101
10' Evaluation
GSF-2
5 " University of Texas
0 AGH& KFA

--
....
E
Col
10'
PNL

.... 5
~
Q,
'-'


" 0
'§;' "
" " o
A • .,'" Q
00
0

~
o 0 0 0 0 o 0 0 000)0

'-'
5

10- '~~~~~~~~~~~Lu~Lu~Lu~Lu~Lu~~~~
l~ 1~ l~ l~ I~ W~ l~ 1~ I~ I~ I~ I~
Neutron energy (MeV)
Fig. A.54. Evaluated and original data for the mean absorbed dose to the stomach (female) in LLAT geometry.

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


I~ - - - Evaluation
v GSF-I
5 " GSF-2
University of Texas
o JAERI
AGH&KFA
....,-.10' PNL
E
Col PTa
.... 5
~
c.
'-'

-
'§;'
~
'-'
10'
5

10-' W-.......w.L........'""'-.........""'"-.......................................J......o.......I..-...........Lu........L..............uL..............u.-.J
10·' 10·' 10"' 10.6 10-S 10~ 10.3 10·' 10·' 10' 10' I~
Neutron energy (MeV)
Fig. A.55. Evaluated and original data for t he mean a bsorbed dose to the thyroid (female) in PA geometry.

- - - Evaluation
5
GSF-\
GSF-2
Uni Austin
c JAERI
1~ AGH& KFA
PNL
5 PTa

10·bL~w.L~'""'-.........-L~........................~~~~~Lu~~........~........~
W·' W·a 10·' 10·' 10·s 10~ 10-3 10-' 10·' 10· 10' 1~
Neutron energy (MeV)
102 Fig. A.56. Evaluated and original data for the effective dose from neut rons in AP geometry.
10'

5 - - - Evaluation
GSF·I
GSF·2
Uni Austin

N -S
C,/
10'

5
0
JAERI
AGH& KFA
PNL
PTS
>
V)
Q.
'-'
10'
~
~
'-'
5

10·~~~~~L.~~~~~~~~~~~~~~~~~~LW
10·' 10·' 10-' 10·' 10.5 10" 10.1 10-' tool to· to' 10'
Neutron energy (MeV)

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


Fig.A.57. Evaluated and original data for the effective dose from neutrons in PAgeometry.

- - - Evaluation
5
GSF-\
GSF·2
Uni Austin
o JAERI

N
-- S
C,/
10'

5
AGH& KFA

V)
>
Q.
'-' to'
5
o

to·bL~~~~~~~~~~~~~~~~~~~~~~~
10.9 10-0 to-' 10·' 10.5 10" 10.1 10-2 10·' 10· 10' to'
Neutron energy (MeV)
Fig. A.5S. Evaluated and original data for the effective dose from neutrons in RLAT geometry.

10'
- - - Evaluation
5
GSF·2
Uni Austin

N
-e C,/
10'

5
0 AGH&KFA

>
rJJ
Q.
'-'

~
~
'-'
10'

5 o
. .•
0

Fig. A.59. Evaluated and original data for the effective dose from neutrons in LLAT geometry. 103
10>
- - - Evaluation
5
GSF-I
GSF-2
Uni Austin

M
- e
Col
10'
5
0 JAERI
AGH& KFA
PTB
>
rr,
c.
'-'
1
~ 10 ox ox

~
'-'

100~~~~~~~~~~~~~~~~~~~~~~~~
9 10.6 5 10·· 10·'
1 1
10. 10. 10'" 10·' 10·' 10. 10· 10 10'
Neutron energy (MeV)
Fig. A.60. Evaluated and original data for the effective dose from neutrons in ROT geometry.

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


10'
5 - - - Evaluation
A GSF-2

00
M-e Col
10'
0

x
JAERI
AGH&KFA
PTB

m > 5

-
m
,..., rr,
r:-: c.
to
1:0 ~
p..
III
p::
;:J
p::
-
~ 10
1

-
Q

10'~~~~~~~~~~wd~wd~wd~~~~~~-u~~

1~ 1~ 1~ 1~ 1~ 1~ 1~ 1~ 1~ 1~ 1~ 10'
Neutron energy (MeV)
104 Fig. A.61. Evaluated and original data for the effective dose from neutrons in ISO geometry.
ANNEX 2. TABLES rn
Q)

~
Photon Data c.;i
><
Q)
~

TABLE A.1- Conversion coefficients" for air kerma per unit (luence, TABLE A.3 -Bone (red marrow) absorbed dose per unit air kerma .;j
K./<l), of monoenergetic photons free-in -air, DTIK., for monoenergetic photons incident in various
geometries on an adult anthropomorphic computational model.
Photon energy (MeV) K.I<P ( pGy em ') These data are presented graphically in Fig. A2 (Annex 1)
0.010 7.43 Photon D-r/K. (Gy/Gy)
0.015 3.12 energy
0.020 1.68 (MeV) AP PA LAT ROT ISO
0.030 0.721
0.010 0.00029 0.00048 0.000 0.00022 0.00014
0.040 0.429
0.015 0.00411 0.00788 0.00197 0.00409 0.00311
0.050 0.323
0.020 0.0144 0.0316 0.00904 0.0167 0.0136
0.060 0.289
0.030 0.0697 0.171 0.0585 0.0932 0.0733
0.080 0.307
0.040 0.211 0.450 0.175 0.262 0.211
0.100 0.371
0.050 0.400 0.772 0.323 0.473 0.385

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


0.150 0.599
0.060 0.573 1.037 0.456 0.660 0.539
0.200 0.856
0.070 0.698 1.212 0.552 0.788 0.645
0.300 1.38
0.080 0.768 1.302 0.603 0.856 0.698
0.400 1.89
0.100 0.822 1.347 0.643 0.900 0.729
0.500 2.38
0.150 0.808 1.254 0.635 0.866 0.706
0.600 2.84
0.200 0.783 1.175 0.629 0.835 0.689
0.800 3.69
0.300 0.761 1.088 0.622 0.804 0.669
1.000 4.47
0.400 0.755 1.043 0.627 0.792 0.665
1.500 6.14
0.500 0.756 1.017 0.637 0.789 0.668
2.000 7.55
0.600 0.761 1.000 0.647 0.790 0.674
3.000 9.96
4.000 12.1 0.800 0.774 0.983 0.667 0.797 0.690
1.000 0.787 0.974 0.686 0.806 0.705
5.000 14.1
2.000 0.833 0.968 0.753 0.845 0.762
6.000 16.1
4.000 0.877 0.980 0.819 0.887 0.821
8.000 20.1
6.000 0.900 0.992 0.851 0.911 0.852
10.000 24.0
8.000 0.916 1.001 0.872 0.927 0.873
• Data from ICRU Report 47 (lCRU, 1992a) using data from 10.000 0.927 1.007 0.889 0.940 0.889
Hubbell (1982).

TABLE A.2 -Bladder absorbed dose per unit air kerma free-in -air, TABLE A.4-Bone (s urface) absorbed dose per unit air kerma
DTiK., for monoenergetic photons incident in various geometries free-in-air, DTiK., for monoenergetic photons incident in various
on an adult anthropomorphic computational model. These data geometries on an adult anthropomorphic computational model.
are presented graphically in Fig. Al (Annex 1) These data are presented graphically in Fig. A3 (Annex 1)
Photon D-r/K. (Gy/Gy) Photon D-r/K. (Gy/Gy)
energy energy
(MeV) AP PA LAT ROT ISO (MeV) AP PA LAT ROT ISO

0.010 0.000 0.000 0.000 0.000 0.000 0.010 0.00143 0.00201 0.00163 0.00161 0.00103
0.015 0.00834 0.000 0.000 0.00140 0.00081 0.015 0.0247 0.0335 0.0218 0.0266 0.0197
0.020 0.0895 0.000 0.000 0.0184 0.0114 0.020 0.101 0.132 0.0884 0.107 0.0826
0.030 0.474 0.0391 0.0254 0.157 0.111 0.030 0.537 0.694 0.422 0.539 0.422
0.040 0.970 0.199 0.121 0.389 0.286 0.040 1.257 1.572 0.928 1.218 0.970
0.050 1.377 0.415 0.250 0.620 0.465 0.050 1.884 2.297 1.344 1.793 1.437
0.060 1.622 0.602 0.358 0.790 0.599 0.060 2.185 2.617 1.526 2.057 1.653
0.070 1.722 0.713 0.421 0.889 0.676 0.070 2.219 2.628 1.541 2.078 1.678
0.080 1.732 0.761 0.450 0.922 0.698 0.080 2.083 2.452 1.432 1.941 1.565
0.100 1.656 0.789 0.476 0.922 0.704 0.100 1.757 2.040 1.206 1.628 1.322 r::JJ
Ol
0.150 1.458 0.752 0.474 0.841 0.661 0.150 1.268 1.448 0.883 1.175 0.965 Ol
,...;
0.200 1.336 0.724 0.466 0.803 0.629 0.200 1.074 1.216 0.763 1.002 0.829
~
0.300 1.231 0.704 0.499 0.777 0.606 0.300 0.938 1.048 0.685 0.879 0.739 to
0.400 1.182 0.709 0.524 0.772 0.609 0.400 0.892 0.987 0.666 0.840 0.713 1::
0
0.500 1.151 0.721 0.542 0.774 0.619 0.500 0.873 0.959 0.663 0.826 0.706 A.
Q)

0.600 1.130 0.733 0.559 0.778 0.632 0.600 0.866 0.943 0.666 0.821 0.707 0:::
0.800 1.102 0.756 0.592 0.790 0.657 0.800 0.863 0.929 0.676 0.821 0.715 ~
0:::
1.000 1.084 0.774 0.620 0.802 0.680 1.000 0.866 0.924 0.690 0.826 0.727 Q
......
2.000 1.041 0.824 0.710 0.849 0.750 2.000 0.885 0.929 0.749 0.858 0.775
4.000 1.015 0.841 0.783 0.898 0.801 4.000 0.912 0.947 0.808 0.893 0.828
6.000 1.000 0.830 0.812 0.920 0.819 6.000 0.928 0.960 0.837 0.911 0.855
8.000 0.986 0.814 0.828 0.932 0.830 8.000 0.938 0.971 0.856 0.927 0.872
10.000 0.973 0.801 0.838 0.940 0.839 10.000 0.947 0.980 0.870 0.939 0.885
105
I'l TABLE A5 - Breast female absorbed dose per unit air kerma TABLE A.7 - Gonads female (ovaries) absorbed dose per unit air
0
:p free-in-air, DTIKa • for monoenergetic photons incident in various kerma free-in-air, DTIKa • for monoenergetic photons incident in
~
;e geometries on an adult anthropomorphic computational model. various geometries on an adult anthropomorphic computational
~
p:: These data are presented graphically in Fig. A.4 (Annex 1) model. These data are presented graphically in Fig. A.6 (Annex 1)
ta
E
OJ
Photon
energy
DrlK, (Gy/Gy) Photon
energy
DTIK, (Gy/Gy)
+>
i< (MeV) AP PA LAT ROT ISO (MeV) AP PA LAT ROT ISO
>il
+>
rn
I'l
0.010 0.0223 0.000 0.00513 0.00869 0.00763 0.010 0.000 0.000 0.000 0.000 0.000
.<Ii 0.015 0.186 0.000 0.0451 0.0747 0.0664 0.015 0.000 0.000 0.000 0.000 0.000
~ 0.020 0.465 0.000 0.128 0.198 0.183 0.020 0.000 0.000 0.000 0.000 0.000
I'l 0.030 0.958 0.0489 0.333 0.449 0.423 0.030 0.158 0.0785 0.00963 0.0660 0.0351
0
:p 0.040 1.296 0.181 0.507 0.655 0.615 0.040 0.511 0.345 0.0996 0.277 0.191
<.)
OJ
+> 0.050 1.522 0.328 0.634 0.811 0.752 0.050 0.846 0.676 0.234 0.527 0.383
...
0
0.060 1.644 0.439 0.724 0.909 0.836 0.060 1.072 0.944 0.345 0.723 0.520
P-
ta 0.070 1.683 0.511 0.765 0.958 0.878 0.070 1.200 1.113 0.414 0.844 0.607
<.)
·So 0.080 1.670 0.545 0.773 0.971 0.883 0.080 1.262 1.201 0.453 0.901 0.653
..s0 0.100 1.600 0.574 0.771 0.958 0.874 0.100 1.282 1.234 0.479 0.926 0.666
;e 0.150 1.449 0.600 0.755 0.912 0.829 0.150 1.185 1.116 0.470 0.882 0.609
~
p:: 0.200 1.361 0.625 0.747 0.875 0.813 0.200 1.106 1.034 0.478 0.841 0.588
0.300 1.264 0.663 0.756 0.851 0.795 0.300 1.017 0.963 0.491 0.810 0.586

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


.S
OJ
rn
0.400 1.214 0.693 0.766 0.851 0.794 0.400 0.972 0.936 0.501 0.796 0.599
0.924 0.511 0.789 0.614
...=' 0.500
0.600
1.184
1.164
0.717
0.737
0.774
0.782
0.854
0.858
0.798
0.804
0.500
0.600
0.948
0.934 0.918 0.522 0.786 0.627
<B
rn 0.800 1.138 0.767 0.799 0.865 0.815 0.800 0.921 0.911 0.542 0.787 0.650
+>
I'l
.~ 1.000 1.123 0.791 0.814 0.872 0.826 1.000 0.918 0.908 0.559 0.793 0.668
<.)
2.000 1.101 0.863 0.866 0.902 0.865 2.000 0.936 0.905 0.624 0.833 0.719
isOJ 0.891
0
4.000 1.084 0.905 0.907 0.923 0.897 4.000 0.981 0.910 0.696 0.769
Co) 6.000 1.068 0.911 0.921 0.927 0.906 6.000 1.013 0.917 0.740 0.926 0.799
I'l 0.949
0 8.000 1.055 0.911 0.927 0.929 0.909 8.000 1.037 0.922 0.772 0.820
·rb
...OJ 10.000 1.042 0.911 0.931 0.930 0.911 10.000 1.056 0.926 0.796 0.966 0.836
>
I'l
0
Co)

TABLE A6 - Colon absorbed dose per unit air kerma free-in-air, TABLEA8-Gonads male (testes) absorbed dose per unit air
DTIKa • for monoenergetic photons incident in various geometries kerma free-in-air, DTIKa • for monoenergetic photons incident in
on an adult anthropomorphic computational model. These data various geometries on an adult anthropomorphic computational
are presented graphically in Fig. A.5 (Annex 1) model. These data are presented graphically in Fig. A. 7 (Annex 1)
Photon DrlK, (Gy/Gy) Photon DriK. (Gy/Gy)
energy energy
(MeV) AP PA RLAT LLAT ROT ISO (MeV) AP PA LAT ROT ISO

0.010 0.000 0.000 0.000 0.000 0.000 0.000 0.010 0.0292 0.000 0.000 0.00744 0.00559
0.015 0.00034 0.000 0.000 0.000 0.00011 0.00009 0.015 0.195 0.000 0.000 0.0571 0.0446
0.020 0.0149 0.000 0.000 0.000 0.00047 0.00008 0.020 0.503 0.000 0.000 0.160 0.138
0.030 0.251 0.0655 0.0306 0.0281 0.0945 0.0619 0.030 1.093 0.0411 0.0230 0.381 0.337
0.040 0.661 0.295 0.133 0.141 0.319 0.224 0.040 1.506 0.160 0.105 0.593 0.516
0.050 1.040 0.581 0.263 0.292 0.566 0.411 0.050 1.767 0.308 0.198 0.763 0.661
0.060 1.289 0.805 0.370 0.419 0.748 0.553 0.060 1.908 0.440 0.264 0.863 0.754
0.070 1.417 0.940 0.436 0.493 0.856 0.638 0.070 1.961 0.524 0.312 0.921 0.802
0.080 1.454 1.006 0.467 0.529 0.902 0.673 0.080 1.953 0.565 0.339 0.946 0.815
ex;, 0.100 1.416 1.036 0.484 0.550 0.907 0.677 0.100 1.855 0.599 0.372 0.934 0.792
O"l 0.150 1.280 0.963 0.462 0.532 0.842 0.640 0.150 1.631 0.629 0.392 0.866 0.744
O"l
.-<
0.200 1.184 0.912 0.459 0.520 0.812 0.614 0.200 1.497 0.641 0.422 0.831 0.720
t-"
10 0.300 1.099 0.873 0.471 0.523 0.789 0.603 0.300 1.366 0.675 0.457 0.794 0.710
"t0 0.400 1.065 0.860 0.486 0.536 0.780 0.606 0.400 1.303 0.705 0.480 0.781 0.712
P-
OJ
0.500 1.046 0.857 0.501 0.551 0.778 0.614 0.500 1.265 0.726 0.503 0.779 0.717
p:: 0.600 1.035 0.858 0.516 0.565 0.780 0.623 0.600 1.238 0.743 0.527 0.780 0.725
~
Co)
0.800
1.000
1.020
1.010
0.863
0.870
0.544
0.570
0.591
0.614
0.790
0.800
0.643
0.662
0.800
1.000
1.202
1.177
0.765
0.782
0.572
0.607
0.789
0.799
0.742
0.757
>-<
2.000 0.985 0.887 0.658 0.694 0.838 0.729 2.000 1.119 0.831 0.703 0.848 0.799
4.000 0.984 0.901 0.733 0.765 0.868 0.788 4.000 1.071 0.864 0.776 0.895 0.843
6.000 0.988 0.908 0.765 0.797 0.879 0.811 6.000 1.043 0.874 0.807 0.916 0.868
8.000 0.984 0.912 0.783 0.816 0.884 0.825 8.000 1.023 0.880 0.822 0.930 0.883
10.000 0.978 0.915 0.797 0.830 0.888 0.834 10.000 1.004 0.884 0.833 0.940 0.893
106
TABLE A9 - Gonads absorbed dose' per unit air kerma free·in·air, TABLE All-Lung absorbed dose per unit air kerma free·in·air, UJ

DTIK" for monoenergetic photons incident in various geometries DTIK., for monoenergetic photons incident in various geometries ~
on an adult anthropomorphic computational model. These data on an adult anthropomorphic computational model. These data ~
are presented graphically in Fig. A8 (Annex 1) are presented graphically in Fig. AIO (Annex 1) C'i
><
Photon Photon '"
~

~
D~K, (Gy/Gy) DTIK, (Gy/Gy)
energy energy
(MeV) AP PA LAT ROT ISO (MeV) AP PA LAT ROT ISO

0.010 0.0146 0.000 0.000 0.00372 0.00280 0.010 0.000 0.000 0.000 0.000 0.000
0.015 0.0970 0.000 0.000 0.0285 0.0223 0.015 0.00175 0.00325 0.00009 0.00111 0.00058
0.020 0.246 0.000 0.000 0.0761 0.0675 0.020 0.0304 0.0482 0.00037 0.0163 0.0100
0.030 0.628 0.0583 0.0165 0.223 0.184 0.030 0.297 0.360 0.0759 0.200 0.141
0.040 1.013 0.248 0.100 0.435 0.356 0.040 0.693 0.780 0.246 0.498 0.375
0.050 1.313 0.492 0.216 0.647 0.527 0.050 1.023 1.117 0.425 0.762 0.592
0.060 1.499 0.703 0.310 0.799 0.638 0.060 1.223 1.319 0.552 0.932 0.727
0.070 1.589 0.834 0.364 0.890 0.709 0.070 1.313 1.414 0.620 1.017 0.800
0.080 1.613 0.896 0.398 0.927 0.743 0.080 1.331 1.435 0.641 1.039 0.817
0.100 1.564 0.917 0.426 0.926 0.727 0.100 1.291 1.397 0.642 1.018 0.806
0.150 1.399 0.858 0.425 0.870 0.669 0.150 1.164 1.264 0.607 0.936 0.749

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


0.200 1.296 0.830 0.461 0.833 0.658 0.200 1.101 1.195 0.596 0.895 0.725
0.300 1.189 0.821 0.476 0.806 0.650 0.300 1.044 1.130 0.597 0.862 0.712
0.400 1.137 0.828 0.486 0.793 0.658 0.400 1.021 1.101 0.610 0.856 0.714
0.500 1.108 0.836 0.502 0.786 0.671 0.500 1.009 1.084 0.625 0.858 0.720
0.600 1.088 0.843 0.520 0.784 0.685 0.600 1.003 1.074 0.639 0.861 0.728
0.800 1.066 0.852 0.555 0.786 0.708 0.800 0.997 1.061 0.664 0.869 0.744
1.000 1.054 0.859 0.584 0.794 0.725 1.000 0.995 1.054 0.686 0.877 0.760
2.000 1.037 0.877 0.667 0.844 0.761 2.000 0.991 1.038 0.764 0.907 0.815
4.000 1.040 0.893 0.741 0.903 0.803 4.000 0.985 1.024 0.829 0.927 0.861
6.000 1.045 0.901 0.779 0.931 0.834 6.000 0.980 1.013 0.852 0.932 0.878
8.000 1.049 0.907 0.803 0.948 0.852 8.000 0.975 1.005 0.863 0.936 0.886
10.000 1.055 0.910 0.819 0.961 0.865 10.000 0.971 0.999 0.870 0.939 0.893
, This table is presented because in the calculation of effective
dose an average value of the mean absorbed dose to the ovaries
and testes is used.

TABLEA10-Liver absorbed dose per unit air kerma free·in·air, TABLE A12 - Oesophagus absorbed dose per unit air kerma
DTIK" for monoenergetic photons incident in various geometries free·in·air, DTIK . , for monoenergetic photons incident in various
on an adult anthropomorphic computational model. These data geometries on an adult anthropomorphic computational model.
are presented graphically in Fig. A9 (Annex 1) These data are presented graphically in Fig. All (Annex 1)
Photon D~K, (Gy/Gy) Photon Dr/K, (Gy/Gy)
energy energy
(MeV) AP PA RLAT LLAT ROT ISO (MeV) AP PA RLAT LLAT ROT ISO

0.010 0.000 0.000 0.000 0.000 0.000 0.000 0.010 0.000 0.000 0.000 0.000 0.000 0.000
0.015 0.00316 0.00063 0.00015 0.000 0.00091 0.00046 0.015 0.000 0.000 0.000 0.000 0.000 0.000
0.020 0.0418 0.0109 0.00285 0.000 0.0139 0.00762 0.020 0.000 0.000 0.00015 0.00005 0.000 0.000
0.030 0.318 0.159 0.142 0.00300 0.159 0.109 0.030 0.0585 0.0435 0.0321 0.0499 0.0507 0.0314
0.040 0.732 0.448 0.427 0.0280 0.420 0.305 0.040 0.268 0.279 0.149 0.188 0.237 0.165
0.050 1.094 0.737 0.711 0.0723 0.674 0.502 0.050 0.522 0 .607 0.298 0.362 0.479 0.341
0.060 1.321 0.934 0.902 0.119 0.846 0.641 0.060 0.721 0.872 0.419 0.510 0.679 0.487
0.070 1.425 1.043 1.001 0.156 0.938 0.721 0.070 0.848 1.032 0.516 0.602 0.800 0.592
0.080 1.446 1.083 1.032 0.180 0.970 0.744 0.080 0.902 1.105 0.572 0.650 0.858 0.638
0.100 1.403 1.077 1.019 0.198 0.959 0.742 0.100 0.926 1.138 0.603 0.662 0.885 0.665 00
0.150 1.261 0.992 0.940 0.213 0.887 0.690 0.150 0.846 0.599 0.840 0.643 CTl
1.083 0.654 CTl
0.200 1.176 0.942 0.899 0.226 0.847 0.667 0.200 0.827 1.018 0.597 0.650 0.805 0.611 ......
0.300 1.094 0.901 0.865 0.251 0.806 0.654 0.300 0.811 0.949 0.604 0.659 0.772 0.607
r-:
Ii:)

0.400 1.056 0.887 0.854 0.277 0.795 0.656 0.400 0.809 0.920 0.619 0.681 0.766 0.624 1:0
0.500 1.034 0.882 0.851 0.301 0.796 0.663 0.500 0.813 0.906 0.637 0.702 0.771 0.642 ~

0.600 1.022 0.881 0.852 0.324 0.800 0.672 0.600 0.818 0.900 0.653 0.719 0.779 0.656 '"
p:;
0.800 1.008 0.882 0.859 0.364 0.811 0.690 0.800 0.828 0.897 0.682 0.746 0.798 0.680 ::>
p:;
1.000 1.002 0.886 0.868 0.399 0.822 0.708 1.000 0.836 0.900 0.704 0.767 0.815 0.698 8
2.000 1.002 0.910 0.906 0.520 0.861 0.772 2.000 0.860 0.921 0.772 0.825 0.869 0.754
4.000 1.006 0.931 0.934 0.626 0.892 0.820 4.000 0.896 0.934 0.830 0.864 0.914 0.804
6.000 1.003 0.935 0.940 0.671 0.902 0.832 6.000 0.920 0.933 0.856 0.878 0.936 0.830
8.000 0 .998 0.934 0.943 0.695 0.906 0.836 8.000 0.934 0.932 0.868 0.888 0.950 0.847
10.000 0.994 0.933 0.945 0.713 0.909 0.837 10.000 0.943 0.930 0.875 0.896 0.961 0.861
107
TABLE A.13 - Remainder absorbed dose per unit air kerma TABLE A.15 - Stomach absorbed dose per unit air kerma
free-in-air, DTIK., for monoenergetic photons incident in various free-in-air, DTIK., for monoenergetic photons incident in various
geometries on an adult anthropomorphic computational model. geometries on an adult anthropomorphic computational model.
These data are presented graphically in Fig. A.12 (Annex 1) These data are presented graphically in Fig. A.14 (Annex 1)
Photon Photon n.,lK, (Gy/Gy)
energy energy
(MeV) AP PA RLAT LLAT ROT ISO (MeV) AP PA RLAT LLAT ROT ISO

0.010 0.00065 0.00066 0.00027 0.00027 0.00048 0.00033 0.010 0.00001 0.000 0.000 0.000 0.000 0.000
0.015 0.00643 0.00643 0.00230 0.00231 0.00438 0.00314 0.015 0.00835 0.000 0.000 0.00014 0.00182 0.00107
0.020 0.0326 0.0367 0.00665 0.00672 0.0201 0.0139 0.020 0.0880 0.000 0.00021 0.00486 0.0249 0.0132
0.030 0.214 0.212 0.0525 0.0695 0.146 0.104 0.030 0.483 0.0489 0.00119 0.149 0.169 0.122
0.040 0.527 0.513 0.169 0.220 0.379 0.284 0.040 0.998 0.230 0.0223 0.431 0.422 0.314
0.050 0.827 0.810 0.305 0.390 0.615 0.471 0.050 1.408 0.459 0.0641 0.705 0.674 0.505
0.060 1.030 1.019 0.412 0.517 0.784 0.605 0.060 1.637 0.643 0.110 0.885 0.844 0.641
0.070 1.136 1.133 0.479 0.595 0.882 0.686 0.070 1.735 0.749 0.145 0.980 0.937 0.717
0.080 1.177 1.177 0.510 0.627 0.920 0.716 0.080 1.740 0.801 0.167 1.008 0.972 0.738
0.100 1.172 1.174 0.529 0.638 0.925 0.719 0.100 1.650 0.815 0.191 1.002 0.962 0.739
0.150 1.070 1.076 0.518 0.616 0.864 0.682 0.150 1.457 0.771 0.207 0.933 0.874 0.688
0.200 1.003 1.013 0.515 0.605 0.826 0.661 0.200 1.355 0.747 0.223 0.889 0.835 0.667

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


0.300 0.945 0.955 0.523 0.606 0.800 0.650 0.300 1.243 0.738 0.252 0.854 0.810 0.644
0.400 0.924 0.932 0.539 0.615 0.794 0.651 0.400 1.185 0.742 0.281 0.846 0.803 0.647
0.500 0.916 0.921 0.556 0.627 0.794 0.657 0.500 1.150 0.748 0.307 0.847 0.803 0.656
0.600 0.913 0.916 0.572 0.640 0.798 0.665 0.600 1.125 0.755 0.332 0.852 0.804 0.665
0.800 0.911 0.913 0.600 0.665 0.807 0.683 0.800 1.093 0.768 0.374 0.863 0.810 0.681
1.000 0.912 0.913 0.625 0.687 0.817 0.701 1.000 1.073 0.780 0.411 0.874 0.819 0.697
2.000 0.923 0.922 0.707 0.757 0.852 0.765 2.000 1.038 0.827 0.533 0.902 0.865 0.768
4.000 0.932 0.935 0.776 0.815 0.886 0.819 4.000 1.023 0.863 0.639 0.915 0.907 0.824
6.000 0.933 0.941 0.804 0.838 0.901 0.839 6.000 1.016 0.874 0.686 0.918 0.921 0.837
8.000 0.933 0.944 0.820 0.851 0.910 0.848 8.000 1.008 0.880 0.713 0.923 0.928 0.843
10.000 0.932 0.948 0.831 0.861 0.916 0.855 10.000 1.002 0.883 0.734 0.927 0.934 0.848

TABLE A.14-Skin absorbed dose per unit air kerma free-in-air, TABLE A.16 - Thyroid absorbed dose per unit air kerma free-in-air,
DTIK., for monoenergetic photons incident in various geometries DTIK., for monoenergetic photons incident in various geometries
on an adult anthropomorphic computational model. These data on an adult anthropomorphic computational model. These data
are presented graphically in Fig. A.13 (Annex 1) are presented graphically in Fig. A.15 (Annex 1)
Photon n.,lK, (Gy/Gy) Photon D.,IK, (Gy/Gy)
energy energy
(MeV) AP PA LAT ROT ISO (MeV) AP PA LAT ROT ISO

0.010 0.235 0.237 0.142 0.200 0.172 0.010 0.00126 0.000 0.000 0.00029 0.00012
0.015 0.377 0.377 0.252 0.331 0.303 0.015 0.0962 0.000 0.00211 0.0227 0.00969
0.020 0.488 0.487 0.343 0.433 0.407 0.020 0.358 0.000 0.0543 0.121 0.0510
0.030 0.654 0.648 0.472 0.581 0.544 0.030 0.910 0.0114 0.335 0.409 0.206
0.040 0.808 0.796 0.578 0.714 0.658 0.040 1.355 0.106 0.650 0.718 0.409
0.050 0.944 0.929 0.669 0.830 0.758 0.050 1.670 0.253 0.892 0.968 0.592
0.060 1.040 1.025 0.738 0.911 0.828 0.060 1.846 0.383 1.062 1.122 0.715
0.070 1.098 1.083 0.790 0.968 0.879 0.070 1.925 0.465 1.146 1.204 0.783
0.080 1.109 1.096 0.796 0.981 0.886 0.080 1.938 0.503 1.179 1.234 0.818
0.100 1.097 1.083 0.805 0.977 0.885 0.100 1.873 0.532 1.188 1.229 0.817
0.150 1.050 1.046 0.795 0.948 0.865 0.150 1.674 0.544 1.131 1.161 0.773
0.200 1.022 1.020 0.789 0.926 0.850 0.200 1.543 0.538 1.091 1.109 0.752
0.300 0.992 0.987 0.787 0.904 0.835 0.300 1.410 0.560 1.059 1.055 0.739
0.400 0.978 0.973 0.791 0.899 0.832 0.400 1.354 0.589 1.057 1.031 0.741
0.500 0.972 0.967 0.797 0.900 0.833 0.500 1.324 0.616 1.063 1.021 0.748
0.600 0.970 0.966 0.805 0.903 0.837 0.600 1.302 0.640 1.069 1.019 0.754
0.800 0.970 0.967 0.819 0.909 0.847 0.800 1.269 0.677 1.076 1.023 0.766
1.000 0.972 0.970 0.833 0.916 0.857 1.000 1.244 0.704 1.081 1.031 0.777
2.000 0.984 0.984 0.879 0.939 0.891 2.000 1.166 0.761 1.093 1.054 0.819
4.000 0.991 0.995 0.910 0.953 0.914 4.000 1.093 0.814 1.075 1.066 0.870
6.000 0.989 0.995 0.917 0.953 0.919 6.000 1.053 0.851 1.052 1.066 0.901
8.000 0.986 0.994 0.920 0.952 0.919 8.000 1.026 0.878 1.036 1.064 0.920
10.000 0.982 0.992 0.921 0.950 0.918 10.000 1.007 0.899 1.023 1.064 0.935
108
TABLE A.17 - Effective dose per unit air kerma free-in -air, E l K., TABLE A.19 - Thymus absorbed dose per unit air kerma cIJ
Cl)

for monoenergetic photons incident in various geometries on an free- in-air, D-r/K. , for monoenergetic photons incident in various ::a
adult anthropomorphic computational model. These reference geometries on an adult anthropomorphic computational model. ~
values are presented graphically in Fig. 8 and Fig. A.16 (Annex 1) These data are presented graphically in Fig. A.18 (Annex 1) c-i
~
Cl)

Photon Photon ~
ElK, (Sv/Gy)
~
D~K, (Gy/Gy)
energy energy
(MeV) AP PA RLAT LLAT ROT ISO (MeV) AP PA LAT ROT ISO

0.010 0.00653 0.00248 0.00172 0.00172 0.00326 0.00271 0.010 0.000 0.000 0.000 0.000 0.000
0.015 0.0402 0.00586 0.00549 0.00549 0.0153 0.0123 0.015 0.0151 0.000 0.000 0.00299 0.00163
0.020 0.122 0.0181 0.0151 0.0155 0.0462 0.0362 0.020 0.161 0.00009 0.000 0.0422 0.0264
0.030 0.416 0.128 0.0782 0.0904 0.191 0.143 0.030 0.700 0.00762 0.0308 0.224 0.159
0.040 0.788 0.370 0.205 0.241 0.426 0.326 0.040 1.246 0.0887 0.151 0.482 0.373
0.050 1.106 0.640 0.345 0.405 0.661 0.511 0.050 1.621 0.223 0.302 0.710 0.572
0.060 1.308 0.846 0.455 0.528 0.828 0.642 0.060 1.826 0.347 0.415 0.853 0.694
0.070 1.407 0.966 0.522 0.598 0.924 0.720 0.070 1.913 0.425 0.488 0.929 0.762
0.080 1.433 1.019 0.554 0.628 0.961 0.749 0.080 1.926 0.463 0.523 0.964 0.788
0.100 1.394 1.030 0.571 0.641 0.960 0.748 0.100 1.866 0.487 0.530 0.974 0.786
0.150 1.256 0.959 0.551 0.620 0.892 0.700 0.150 1.640 0.505 0.536 0.901 0.747

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


0.200 1.173 0.915 0.549 0.615 0.854 0.679 0.200 1.499 0.498 0.549 0.863 0.720
0.300 1.093 0.880 0.557 0.615 0.824 0.664 0.300 1.359 0.489 0.580 0.846 0.703
0.400 1.056 0.871 0.570 0.623 0.814 0.667 0.400 1.289 0.496 0.606 0.840 0.704
0.500 1.036 0.869 0.585 0.635 0.812 0.675 0.500 1.246 0.510 0.628 0.836 0.710
0.600 1.024 0.870 0.600 0.647 0.814 0.684 0.600 1.215 0.525 0.646 0.834 0.715
0.800 1.010 0.875 0.628 0.670 0.821 0.703 0.800 1.171 0.553 0.675 0.831 0.726
1.000 1.003 0.880 0.651 0.691 0.831 0.719 1.000 1.141 0.577 0.700 0.832 0.738
2.000 0.992 0.901 0.728 0.757 0.871 0.774 2.000 1.063 0.645 0.779 0.850 0.786
4.000 0.993 0.918 0.796 0.813 0.909 0.824 4.000 1.003 0.715 0.840 0.883 0.835
6.000 0.993 0.924 0.827 0.836 0.925 0.846 6.000 0.972 0.758 0.861 0.905 0.856
8.000 0.991 0.927 0.846 0.850 0.934 0.859 8.000 0.950 0.789 0.872 0.920 0.867
10.000 0.990 0.929 0.860 0.859 0.941 0.868 10.000 0.933 0.813 0.880 0.932 0.875

TABLE A.18 - Eye lens absorbed dose p er unit air kerma TABLE A.20 - Uterus absorbed dose per unit air kerma free·in-air,
free-in-air, D-r/K., for monoenergetic photons incident in various DTIK., for monoenergetic photons incident in various geometries
geometries on an adult anthropomorphic computational model. on an adult anthropomorphic computational model. These data
These data are presented graphically in Fig. A.17 (Annex 1) are presented graphically in Fig. A.19 (Annex 1)
Photon D~K, (Gy/Gy ) Photon D~K, (Gy/Gy)
energy energy
(MeV) AP PA LAT ROT ISO (MeV) AP PA LAT ROT ISO

0.010 0.304 0.000 0.0880 0.114 0.0877 0.010 0.000 0.000 0.000 0.000 0.000
0.015 0.664 0.000 0.252 0.287 0.236 0.015 0.00024 0.000 0.000 0.000 0.000
0.020 0.912 0.000 0.390 0.423 0.365 0.020 0.00133 0.000 0.000 0.000 0.000
0.030 1.197 0.000 0.579 0.588 0.523 0.030 0.217 0.0700 0.00817 0.0759 0.0491
0.040 1.334 0.0186 0.718 0.694 0.639 0.040 0.606 0.309 0.0850 0.283 0.195
0.050 1.419 0.0521 0.838 0.793 0.742 0.050 0.966 0.594 0.201 0.524 0.371
0.060 1.492 0.0837 0.930 0.886 0.812 0.060 1.209 0.814 0.303 0.708 0.511
0.070 1.536 0.122 0.988 0.958 0.857 0.070 1.333 0.955 0.379 0.816 0.596
0.080 1.550 0.156 1.023 0.999 0.882 0.080 1.381 1.025 0.412 0.862 0.630
0.100 1.530 0.193 1.049 1.030 0.907 0.100 1.376 1.054 0.431 0.874 0.636 a:J
Ol
0.150 1.425 0.241 1.024 1.017 0.894 0.150 1.224 0.973 0.439 0.811 0.609 Ol
0.200 1.357 0.262 1.020 0.994 0.868 0.200 1.126 0.910 0.440 0.772 0.586
.....
~
0.300 1.280 0.295 1.015 0.958 0.846 0.300 1.032 0.866 0.450 0.743 0.562 lQ

0.400 1.232 0.333 1.013 0.935 0.839 0.400 0.988 0.857 0.462 0.739 0.564 1::
0
0.500 1.199 0.369 1.012 0.921 0.836 0.500 0.965 0.854 0.477 0.742 0.574 p..
Cl)

0.600 1.174 0.401 1.010 0.913 0.835 0.600 0.952 0.853 0.494 0.747 0.586 r:t:
0.800
1.000
1.138
1.113
0.453
0.495
1.007
1.004
0.908
0.909
0.837
0.843
0.800
1.000
0.941
0.937
0.853
0.854
0.529
0.561
0.759
0.769
0.608
0.627
~
U
.....
2.000 1.047 0.618 1.005 0.943 0.878 2.000 0.929 0.862 0.667 0.798 0.692
4.000 0.995 0.723 1.015 0.995 0.917 4.000 0.915 0.868 0.742 0.826 0.752
6.000 0.967 0.775 1.022 1.024 0.936 6.000 0.902 0.867 0.765 0.844 0.780
8.000 0.946 0.807 1.028 1.044 0.950 8.000 0.893 0.863 0.775 0.855 0.798
10.000 0.931 0.833 1.034 1.063 0.963 10.000 0.885 0.859 0.782 0.864 0.810
109
TABLE A.21- Conversion coefficients a for the ambient dose TABLE A.23 - Conversion coefficients from air kerma free-in-air to
equivalent, H*(10), and directional dose equivalent, H'(0.07, 0°), H'(0.07, 0°) and angular dependence factors, R(10, a) (Dimbylow
from photon fluence and air kerma free-in-air and Francis, 1989)
Photon Photon RatioH'(0.07, a)!H'(0.07, 0")
energy H*(10)!K, H'(0.07,O")IK, K/cf> H*(lO)/cf> H'(0.07,O")!cf> energy H'(0.07, O")!K, ----~~~--.:...-.:..=~--.:...~---
(MeV) (Sv/Gy) (Sv/Gy) (pGycm2) (pSvcm2) (pSvcm2) (MeV) (Sv/Gy) 0" 15" 30" 45" 60" 75" 90" 180"

0.010 0.008 0.95 7.60 0.061 7.20 0.005 0.76 1.00 0.96 0.87 0.79 0.41 0.00 0.00 0.00
0.015 0.26 0.99 3.21 0.83 3.19 0.010 0.95 1.00 0.99 0.98 0.98 0.96 0.89 0.19 0.00
0.020 0.61 1.05 1.73 1.05 1.81 0.020 1.05 1.00 1.00 0.99 1.00 1.00 0.98 0.54 0.00
0.030 1.10 1.22 0.739 0.81 0.90 0.030 1.22 1.00 0.99 0.99 0.99 0.98 0.94 0.62 0.00
0.040 1.47 1.41 0.438 0.64 0.62 0.050 1.53 1.00 0.99 0.98 0.98 0.97 0.92 0.69 0.02
0.050 1.67 1.53 0.328 0.55 0.50 0.100 1.55 1.00 0.99 0.99 0.99 0.98 0.94 0.77 0.05
0.060 1.74 1.59 0.292 0.51 0.47 0.150 1.42 1.00 0.99 0.99 0.99 0.99 0.97 0.87 0.07
0.080 1.72 1.61 0.308 0.53 0.49 0.300 1.31 1.00 1.00 1.00 1.00 1.02 1.00 0.89 0.10
0.100 1.65 1.55 0.372 0.61 0.58 0.662 1.20 1.00 1.00 1.00 1.00 1.00 0.98 0.89 0.18
0.150 1.49 1.42 0.600 0.89 0.85 1.25 1.16 1.00 1.00 1.00 1.00 1.00 0.98 0.90 0.30
0.200 1.40 1.34 0.856 1.20 1.15 2 1.14 1.00 1.00 1.00 1.00 1.00 0.98 0.90 0.39
0.300 1.31 1.31 1.38 1.80 1.80 3 1.13 1.00 1.00 1.00 1.00 1.00 0.98 0.90 0.46
0.400 1.26 1.26 1.89 2.38 2.38 5 1.11 1.00 1.00 1.00 1.00 1.00 0.98 0.91 0.54
0.500 1.23 1.23 2.38 2.93 2.93 10 1.10 1.00 1.00 1.00 1.00 1.00 0.98 0.94 0.63

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


0.600 1.21 1.21 2.84 3.44 3.44
0.800 1.19 1.19 3.69 4.38 4.38
1 1.17 1.17 4.47 5.20 5.20
1.5 1.15 1.15 6.12 6.90 6.90
2 1.14 1.14 7.51 8.60 8.60
3 1.13 1.13 9.89 11.1 11.1
4 1.12 1.12 12.0 13.4 13.4
5 1.11 1.11 13.9 15.5 15.5
6 1.11 1.11 15.8 17.6 17.6
8 1.11 1.11 19.5 21.6 21.6
10 1.10 1.10 23.2 25.6 25.6
a Data compiled from ICRU Report 47 (1992a) using Hubbell
and Seltzer (1995). The K.I<P data are slightly different from those
used for the protection quantities (see Table A.1) which used
earlier data from Hubbell (1982).

TABLE A.24- Conversion coefficients from air kerma free-in-air to


Hi10, 0°) in an ICRU slab and angular dependence factors
R(10, a) (Gross wendt et al., nd)
Photon Ratio Hp(lO, a)IHp(lO, 0")
energy Hp(lO,O")IK,
(MeV) (Sv/Gy) 0" 15" 30" 45" 60" 75"

0.010 0.009 1.000 0.889 0.556 0.222 0.000 0.000


0.0125 0.098 1.000 0.929 0.704 0.388 0.102 0.000
0.015 0.264 1.000 0.966 0.822 0.576 0.261 0.030
0.0175 0.445 1.000 0.971 0.879 0.701 0.416 0.092
TABLE A.22 - Conversion coefficients from air kerma free-in-air to 0.020 0.611 1.000 0.982 0.913 0.763 0.520 0.167
H'(10, 0°) and angular dependence factors, R(10, a) (from 0.025 0.883 1.000 0.980 0.937 0.832 0.650 0.319
graphical data in ICRU (1992a); Grosswendt and Hohlfeld 0.030 1.112 1.000 0.984 0.950 0.868 0.716 0.411
(1982)) 0.040 1.490 1.000 0.986 0.959 0.894 0.760 0.494
0.050 1.766 1.000 0.988 0.963 0.891 0.779 0.526
Photon Ratio H'(10, a)!H'(10, 0") 0.060 1.892 1.000 0.988 0.969 0.911 0.793 0.561
energy H'(lO,O")IK, - - - - - - - - - - - - - - - -
(MeV) (Sv/Gy) 0" 15" 30" 45" 60" 75" 90" 180" 0.080 1.903 1.000 0.997 0.970 0.919 0.809 0.594
0.100 1.811 1.000 0.992 0.972 0.927 0.834 0.612
0.015 0.26 1.00 0.85 0.63 0.42 0.20 0.05 0.00 0.00 0.125 1.696 1.000 0.998 0.980 0.938 0.857 0.647
0.020 0.61 1.00 0.94 0.83 0.67 0.46 0.22 0.06 0.00 0.150 1.607 1.000 0.997 0.984 0.947 0.871 0.677
0.030 1.10 1.00 0.98 0.93 0.85 0.69 0.47 0.23 0.00 0.200 1.492 1.000 0.997 0.991 0.959 0.900 0.724
0.050 1.67 1.00 1.00 0.96 0.88 0.80 0.61 0.37 0.02 0.300 1.369 1.000 1.000 0.996 0.984 0.931 0.771
0.100 1.65 1.00 1.00 0.98 0.93 0.86 0.70 0.48 0.04 0.400 1.300 1.000 1.004 1.001 0.993 0.955 0.814
0.150 1.49 1.00 1.00 0.98 0.95 0.88 0.75 0.56 0.08 0.500 1.256 1.000 1.005 1.002 1.001 0.968 0.846
0.300 1.31 1.00 1.00 0.99 0.96 0.91 0.82 0.67 0.13 0.600 1.226 1.000 1.005 1.004 1.003 0.975 0.868
0.662 1.20 1.00 1.00 1.00 0.97 0.95 0.87 0.76 0.23 0.800 1.190 1.000 1.001 1.003 1.007 0.987 0.892
1.25 1.16 1.00 1.00 1.00 0.99 0.97 0.92 0.82 0.34 1 1.167 1.000 1.000 0.996 1.009 0.990 0.910
2 1.14 1.00 1.00 1.00 1.00 0.98 0.93 0.85 0.44 1.5 1.139 1.000 1.002 1.003 1.006 0.997 0.934
3 1.13 1.00 1.00 1.00 1.00 0.98 0.94 0.86 0.49 3 1.117 1.000 1.005 1.010 0.998 0.998 0.958
5 1.11 1.00 1.00 1.00 1.00 0.98 0.94 0.88 0.56 6 1.109 1.000 1.003 1.003 0.992 0.997 0.995
10 1.10 1.00 1.00 1.00 1.00 0.98 0.95 0.90 0.62 10 1.111 1.000 0.998 0.995 0.989 0.992 0.966
110
rJl
TABLEA.25 - Conversion coefficients from air kerma free-in-air to
HlO.07, 0°) in an ICRU slab and angular dependence factors,
Neutron Data OJ
:a
R(10, a) (Gross wendt et ai., nd) TABLE A.26 - Bladder absorbed dose per unit neutron fluence, ~
DTI<J>, in units ofpGy cm2 for monoenergetic neutrons incident in N
Photon various geometries on an adult anthropomorphic computational ><
OJ
Ratio Hp(O.07, a)IHp (O.07, 0°)
energy Hp(O.07,00)IK, ~
model. These data are presented graphically in
(MeV) (SvIGy) 0° 15° 30° 45° 60° 75°
Fig. A.20 (Annex 1)
.;j
0.005 0.750 1.000 0.991 0.956 0.895 0.769 0.457
Energy
0.010 0.947 1.000 0.996 0.994 0.987 0.964 0.904 (MeV) AP PA LAT ROT ISO
0.015 0.981 1.000 1.000 1.001 0.994 0.992 0.954
0.020 1.045 1.000 0.996 0.996 0.987 0.982 0.948 1.0 X 10- 9 1.28 0.50 0.18 0.55 0.46
0.030 1.230 1.000 0.990 0.989 0.972 0.946 0.897 1.0 X 10- 8 1.63 0.65 0.24 0.67 0.57
0.040 1.444 1.000 0.994 0.990 0.965 0.923 0.857 2.5 X 10- 8 1.94 0.77 0.28 0.81 0.66
0.050 1.632 1.000 0.994 0.979 0.954 0.907 0.828 1.0 X 10- 7 2.65 1.02 0.36 1.13 0.83
0.060 1.716 1.000 0.995 0.984 0.961 0.913 0.837 2.0 X 10- 7 3.03 1.14 0.40 1.29 0.92
0.080 1.732 1.000 0.994 0.991 0.966 0.927 0.855 5.0 X 10- 7 3.51 1.31 0.46 1.48 1.04
0.100 1.669 1.000 0.993 0.990 0.973 0.946 0.887 1.0 X 10- 6 3.84 1.42 0.50 1.61 1.13
0.150 1.518 1.000 1.001 1.005 0.995 0.977 0.950 2.0 X 10- 6 4.06 1.52 0.54 1.72 1.20
0.200 1.432 1.000 1.001 1.001 1.003 0.997 0.981 5.0 X 10- 6 4.24 1.63 0.59 1.81 1.29
10- 5

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


0.300 1.336 1.000 1.002 1.007 1.010 1.019 1.013 1.0 X 4.28 1.69 0.61 1.84 1.33
0.400 1.280 1.000 1.002 1.009 1.016 1.032 1.035 2.0 X 10- 5 4.27 1.73 0.63 1.85 1.35
0.500 1.244 1.000 1.002 1.008 1.020 1.040 1.054 5.0 X 10- 5 4.19 1.75 0.63 1.82 1.36
0.600 1.220 1.000 1.003 1.009 1.019 1.043 1.057 1.0 X 10- 4 4.11 1.76 0.63 1.80 1.35
0.800 1.189 1.000 1.001 1.008 1.019 1.043 1.062 2.0 X 10- 4 4.05 1.74 0.62 1.78 1.33
1.000 1.173 1.000 1.002 1.005 1.016 1.038 1.060 5.0 X 10- 4 3.99 1.71 0.61 1.76 1.30
1.0 X 10- 3 3.97 1.69 0.60 1.75 1.28
2.0 X 10- 3 3.98 1.69 0.58 1.73 1.25
5.0 X 10- 3 4.01 1.69 0.58 1.74 1.24
1.0 X 10- 2 3.97 1.71 0.58 1.76 1.26
2.0 X 10- 2 4.00 1.72 0.60 1.76 1.30
3.0 X 10- 2 4.01 1.74 0.61 1.78 1.34
5.0 X 10- 2 4.08 1.79 0.64 1.85 1.42
7.0 X 10- 2 4.22 1.83 0.67 1.93 1.50
1.0 X 10- 1 4.51 1.90 0.71 2.05 1.60
1.5 X 10- 1 5.18 1.96 0.75 2.24 1.72
2.0 X 10- 1 5.87 2.03 0.80 2.43 1.85
3.0 X 10- 1 7.24 2.20 0.89 2.86 2.12
5.0 X 10- 1 9.84 2.57 1.09 3.77 2.69
7.0 X 10- 1 12.3 2.91 1.25 4.72 3.33
9.0 X 10- 1 14.7 3.36 1.49 5.72 3.99
1.0 X 10° 15.8 3.63 1.64 6.22 4.33
1.2 X 10° 18.0 4.42 2.10 7.27 5.10
2.0 X 100 25.8 8.19 4.79 11.4 8.43
3.0 X 100 34.0 13.4 8.48 16.3 12.7
4.0 X 10° 40.5 18.3 12.0 20.9 16.9
5.0 X 100 46.0 22.5 15.3 25.0 20.6
6.0 X 100 50.6 26.4 18.4 28.9 23.6
7.0 X 10° 54.6 30.1 21.3 32.4 26.3
8.0 X 100 58.0 33.7 24.0 35.7 28.8
9.0 X 100 61.1 37.0 26.6 38.7 31.1
1.0 X 10 1 63.7 40.2 29.0 41.5 33.3
1.2 X 10 1 68.2 45.7 33.3 46.0 37.5
1.4 X 101 71.7 50.3 37.0 49.9 41.0
1.5 X 10 1 73.2 52.2 38.7 51.6 42.5
1.6 X 10 1 74.5 53.8 40.3 53.2 43.9
1.8 X 101 76.8 56.7 43.3 56.0 46.3
2.0 X 10 1 78.7 59.1 46.0 58.6 48.1 rX)
0')

3.0 X 10 1 84.5 67.1 57.0 67.5 na a 0')


,.....
5.0 X 10 1 88.6 77.4 72.6 78.5 na ".:
LO
7.5 X 101 89.3 89.3 86.0 88.0 na -+"
....
1.0 X 102 88.5 101 96.6 95.8 na 0
0-
1.3 X 102 87.0 113 106 103 na
~
OJ

1.5 X 102 85.3 125 114 109 na ;:J


1.8 X 102 83.1 138 124 117 na ~
C)
......
a Not available.

111
>=:
0
TABLE A.27 - Bone (red marrow) absorbed dose per unit neutron TABLE A.28 - Bone (surface) absorbed dose per unit neutron
:g fluence, Dr/<P, in units ofpGy cm2 for monoenergetic neutrons fluence, DTI<P, in units ofpGy cm2 for monoenergetic neutrons
;.a incident in various geometries on an adult anthropomorphic incident in various geometries on an adult anthropomorphic
ca
~ computational model. These data are presented graphically in computational model. These data are presented graphically in
<a Fig. A.21 (Annex 1) Fig. A.22 (Annex 1)
EQ)
Energy Energy
t;l (MeV) AP PA LAT ROT ISO (MeV) AP PA LAT ROT ISO
ril
+'
00
>=: 1.0 X 10- 9 0.61 1.14 0.37 0.62 0.48 1.0 X 10- 9 0.77 0.94 0.47 0.67 0.54
'8 1.0 X 10- 8 0.76 1.41 0.48 0.80 0.62 1.0 X 10- 8 0.95 1.15 0.59 0.85 0.62
~ 2.5 X 10- 8 0.91 1.61 0.56 0.94 0.71 2.5 X 10- 8 1.10 1.34 0.69 1.00 0.72
>=: 1.0 X 10- 7 1.0 X 10- 7
0 1.21 2.07 0.71 1.21 0.88 1.43 1.69 0.88 1.26 0.92
:p
<..> 2.0 X 10- 7 1.38 2.31 0.80 1.35 0.97 2.0 X 10- 7 1.60 1.88 0.98 1.39 1.01
Q)
+'
0
5.0 X 10- 7 1.59 2.62 0.91 1.52 1.09 5.0 X 10- 7 1.80 2.12 1.09 1.56 1.13
&:: 1.0 X 10- 6 1.72 2.82 0.99 1.63 1.18 1.0 X 10- 6 1.93 2.29 1.17 1.67 1.21
<a<..> 2.0 X 10- 6 1.83 2.99 1.05 1.72 1.24 2.0 X 10- 6 2.03 2.40 1.22 1.75 1.26
'6b 5.0 X 10- 6 1.93 3.12 1.10 1.81 1.29 5.0 X 10- 6 2.09 2.48 1.26 1.81 1.30
0
'0 1.0 X 10- 5 1.97 3.1 1.12 1.85 1.31 1.0 X 10- 5 2.10 2.50 1.27 1.82 1.31
;.a 2.0 X 10- 5 1.98 3.16 1.13 1.85 1.33 2.0 X 10- 5 2.08 2.50 1.26 1.80 1.30
ca
~ 5.0 X 10- 5 1.96 3.11 1.12 1.82 1.32 5.0 X 10- 5 2.03 2.47 1.23 1.76 1.27
.S 1.0 X 10- 4 1.0 X 10- 4

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


1.93 3.04 1.11 1.79 1.31 1.98 2.43 1.20 1.72 1.24
Q)
00 2.0 X 10- 4 1.89 2.97 1.08 1.75 1.28 2.0 X 10- 4 1.93 2.39 1.17 1.67 1.20
;:S
... 5.0 X 10- 4 1.83 2.89 1.05 1.71 1.24 5.0 X 10- 4 1.88 2.33 1.13 1.61 1.16
..s
00
1.0 X 10- 3 1.78 2.84 1.03 1.69 1.21 1.0 X 10- 3 1.86 2.29 1.10 1.58 1.13
+' 2.0 X 10- 3 1.75 2.81 1.01 1.68 1.18 2.0 X 10- 3 1.86 2.24 1.09 1.56 1.12
>=:
Q)
5.0 X 10- 3 1.76 2.81 1.01 1.69 1.18 5.0 X 10- 3 1.88 2.22 1.09 1.56 1.13
'<l
!:S 1.0 X 10- 2 1.81 2.87 1.03 1.74 1.21 1.0 X 10- 2 1.91 2.26 1.12 1.61 1.18
Q)
0 2.0 X 10- 2 1.91 3.01 1.09 1.79 1.29 2.0 X 10- 2 1.97 2.36 1.17 1.68 1.24
U 3.0 X 10- 2 2.00 3.13 1.15 1.86 1.36 3.0 X 10- 2 2.02 2.45 1.22 1.75 1.31
>=:
.~ 5.0 X 10- 2 2.15 3.37 1.25 1.99 1.50 5.0 X 10- 2 2.13 2.65 1.34 1.89 1.44
...
00
Q)
7.0 X 10- 2 2.29 3.63 1.35 2.12 1.62 7.0 X 10- 2 2.27 2.85 1.46 2.05 1.57
>
>=:
1.0 X 10- 1 2.46 4.03 1.49 2.32 1.78 1.0 X 10- 1 2.51 3.16 1.66 2.28 1.75
U
0 1.5 X 10- 1 2.71 4.65 1.71 2.68 2.04 1.5 X 10- 1 2.92 3.65 2.00 2.70 2.08
2.0 X 10- 1 2.92 5.26 1.92 3.03 2.28 2.0 X 10- 1 3.32 4.12 2.33 3.10 2.38
3.0 X 10- 1 3.28 6.41 2.32 3.68 2.77 3.0 X 10- 1 4.08 5.01 2.95 3.84 2.99
5.0 X 10- 1 4.08 8.56 3.11 4.92 3.70 5.0 X 10- 1 5.48 6.66 4.08 5.21 4.12
7.0 X 10- 1 5.09 10.6 3.90 6.12 4.61 7.0 X 10- 1 6.79 8.28 5.14 6.48 5.14
9.0 X 10- 1 6.21 12.6 4.71 7.27 5.49 9.0 X 10- 1 8.04 9.80 6.14 7.69 6.11
1.0 X 10° 6.79 13.5 5.12 7.83 5.93 1.0 X 10° 8.64 10.5 6.62 8.27 6.58
1.2 X 10° 7.99 15.5 6.07 9.08 6.85 1.2 X 10° 9.79 11.9 7.54 9.41 7.49
2.0 X 10° 12.8 22.5 9.99 13.9 10.3 2.0 X 10° 13.9 16.6 10.9 13.5 10.8
3.0 X 10° 18.3 29.7 14.3 19.2 14.3 3.0 X 10° 18.3 21.5 14.4 17.8 14.5
4.0 X 10° 23.2 35.2 17.8 23.8 17.9 4.0 X 10° 22.1 25.6 17.5 21.6 17.8
5.0 X 10° 27.4 39.3 20.9 27.8 21.1 5.0 X 10° 25.5 29.2 20.4 24.9 20.8
6.0 X 10° 31.1 42.6 23.6 31.1 23.8 6.0 X 10° 28.7 32.4 22.9 27.8 23.7
7.0 X 10° 34.5 45.5 26.0 34.0 26.3 7.0 X 10° 31.7 35.3 25.3 30.6 26.3
8.0 X 10° 37.5 48.1 28.2 36.7 28.7 8.0 X 10° 34.4 38.0 27.5 33.1 28.6
9.0 X 10° 40.2 50.5 30.2 39.1 30.9 9.0 X 10° 37.0 40.4 29.5 35.4 30.7
1.0 X 101 42.6 52.7 32.1 41.3 33.1 1.0 X 101 39.3 42.7 31.4 37.4 32.6
1.2 X 101 46.6 56.6 35.5 44.8 37.6 1.2 X 101 43.3 46.7 34.7 41.1 35.5
1.4 X 101 49.9 59.6 38.6 47.7 41.4 1.4 X 101 46.6 50.1 37.7 44.1 37.9
1.5 X 10 1 51.2 60.9 40.0 49.0 43.1 1.5 X 101 48.0 51.5 39.0 45.4 39.1
1.6 X 101 52.4 62.0 41.4 50.1 44.5 1.6 X 101 49.3 52.8 40.2 46.6 40.2
1.8 X 101 54.5 63.7 44.0 52.1 46.8 1.8 X 10 1 51.6 55.0 42.6 48.7 42.6
2.0 X 101 56.2 65.1 46.4 53.8 48.4 2.0 X 101 53.5 56.9 45.1 50.5 45.6
3.0 X 101 62.0 68.9 53.3 59.4 na' 3.0 X 101 60.3 63.3 52.6 57.1 na"
00
en 5.0 X 101 68.8 71.8 61.6 65.9 na 5.0 X 101 68.4 69.9 61.8 65.2 na
en
,...; 7.5 X 101 75.0 74.0 69.0 71.7 na 7.5 X 101 75.3 74.3 69.7 72.2 na
~ 1.0 X 102 80.5 76.2 75.3 76.8 na 1.0 X 102 81.0 77.3 76.2 77.7 na
lC
1:: 1.3 X 102 85.6 78.5 81.4 81.7 na 1.3 X 102 86.0 79.5 82.0 82.5 na
0
~
1.5 X 102 90.5 81.0 87.3 86.5 na 1.5 X 102 90.6 81.4 87.4 86.8 na
Q)
~ 1.8 X 102 96.1 84.1 94.4 92.2 na 1.8 X 102 95.7 83.3 93.7 91.5 na
::> " Not available. • Not available.
~

-
U

112
m
TABLE A.29 - Breast (female) absorbed dose per unit neutron TABLEA.30-Colon absorbed dose per unit neutron fluence, DTI <P, Q)

~
fluence, DTI<P, in units ofpGy cm2 for monoenergetic neutrons in units ofpGy cm2 for monoenergetic neutrons incident in
incident in various geometries on an adult anthropomorphic various geometries on an adult anthropomorphic computational
computational model, These data are presented graphically in model, These data are presented graphically in c-i
><
Fig. A.23 (Annex 1) Fig. A.24 (Annex 1) Q)

Energy
(MeV) AP PA LAT ROT ISO
Energy
(MeV) AP PA RLAT LLAT ROT ISO
J
1.0 X 10- 9 1.68 0.28 0.38 0.69 0.59 1.0 X 10- 9 0.89 0.77 0.11 0.45 0.53 0.40
1.0 X 10- 8 1.92 0.31 0.45 0.84 0.67 1.0 X 10- 8 1.06 0.96 0.16 0.48 0.66 0.51
2.5 X 10- 8 2.11 0.37 0.50 0.93 0.73 2.5 X 10- 8 1.28 1.13 0.19 0.53 0.80 0.59
1.0 X 10- 7 2.42 0.50 0.59 1.08 0.86 1.0 X 10- 7 1.79 1.42 0.28 0.64 1.08 0.75
2.0 X 10- 7 2.58 0.57 0.64 1.16 0.92 2.0 X 10- 7 2.09 1.58 0.32 0.72 1.22 0.85
5.0 X 10- 7 2.75 0.68 0.72 1.27 0.99 5.0 X 10- 7 2.48 1.80 0.39 0.83 1.40 0.97
1.0 X 10- 6 2.85 0.75 0.77 1.34 1.04 1.0 X 10- 6 2.75 1.96 0.44 0.93 1.51 1.07
2.0 X 10- 6 2.91 0.80 0.79 1.39 1.06 2.0 X 10- 6 2.91 2.07 0.46 1.00 1.61 1.14
5.0 X 10- 6 2.91 0.85 0.81 1.39 1.08 5.0 X 10- 6 3.02 2.19 0.49 1.08 1.71 1.22
1.0 X 10- 5 2.86 0.88 0.80 1.37 1.08 1.0 X 10- 5 3.04 2.25 0.50 1.14 1.76 1.27
2.0 X 10- 5 2.79 0.88 0.80 1.33 1.07 2.0 X 10- 5 3.05 2.29 0.50 1.18 1.78 1.30

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


5.0 X 10- 5 2.66 0.88 0.78 1.27 1.05 5.0 X 10- 5 3.05 2.31 0.51 1.23 1.78 1.32
1.0 X 10- 4 2.56 0.88 0.76 1.23 1.02 1.0 X 10- 4 3.04 2.31 0.50 1.26 1.77 1.33
2.0 X 10- 4 2.46 0.88 0.74 1.18 0.97 2.0 X 10- 4 3.04 2.30 0.50 1.27 1.75 1.32
5.0 X 10- 4 2.36 0.87 0.71 1.15 0.92 5.0 X 10- 4 3.04 2.29 0.50 1.28 1.72 1.29
1.0 X 10- 3 2.32 0.86 0.70 1.16 0.89 1.0 X 10- 3 3.04 2.28 0.50 1.28 1.69 1.28
2.0 X 10- 3 2.33 0.86 0.69 1.17 0.87 2.0 X 10- 3 3.05 2.27 0.50 1.29 1.67 1.27
5.0 X 10- 3 2.44 0.86 0.70 1.22 0.89 5.0 X 10- 3 3.06 2.27 0.50 1.31 1.65 1.27
1.0 X 10- 2 2.63 0.87 0.74 1.30 0.97 1.0 X 10- 2 3.07 2.30 0.50 1.33 1.66 1.28
2.0 X 10- 2 2.92 0.85 0.81 1.44 1.14 2.0 X 10- 2 3.04 2.33 0.50 1.31 1.69 1.31
3.0 X 10- 2 3.15 0.86 0.90 1.57 1.29 3.0 X 10- 2 3.04 2.37 0.50 1.32 1.72 1.34
5.0 X 10- 2 3.65 0.88 1.09 1.82 1.59 5.0 X 10- 2 3.05 2.46 0.51 1.35 1.79 1.39
7.0 X 10- 2 4.23 0.90 1.27 2.06 1.87 7.0 X 10- 2 3.10 2.55 0.52 1.39 1.85 1.45
1.0 X 10- 1 5.16 0.95 1.53 2.40 2.28 1.0 X 10- 1 3.20 2.67 0.53 1.45 1.93 1.52
1.5 X 10- 1 6.76 0.98 2.00 3.18 2.98 1.5 X 10- 1 3.43 2.84 0.55 1.52 2.04 1.61
2.0 X 10- 1 8.30 1.03 2.45 3.94 3.64 2.0 X 10- 1 3.66 3.00 0.57 1.60 2.16 1.70
3.0 X 10- 1 11.2 1.17 3.30 5.36 4.82 3.0 X 10- 1 4.22 3.31 0.62 1.80 2.45 1.86
5.0 X 10- 1 15.9 1.55 4.86 7.84 6.89 5.0 X 10- 1 5.49 3.90 0.77 2.29 3.05 2.23
7.0 X 10- 1 19.5 2.02 6.24 9.91 8.69 7.0 X 10- 1 6.94 4.53 0.92 2.86 3.69 2.67
9.0 X 10- 1 22.5 2.64 7.51 11.6 10.3 9.0 X 10- 1 8.52 5.40 1.12 3.51 4.47 3.14
1.0 X 10° 23.8 3.01 8.11 12.4 11.1 1.0 X 10° 9.35 5.93 1.26 3.85 4.92 3.39
1.2 X 10° 26.1 3.90 9.33 13.7 12.5 1.2 X 10° 11.1 7.15 1.61 4.65 5.92 4.07
2.0 X 10° 32.9 7.70 13.71 17.8 17.3 2.0 X 10° 17.4 12.6 3.61 8.44 10.4 7.14
3.0 X 10° 38.6 12.4 17.8 21.6 22.1 3.0 X 10° 24.5 18.7 6.04 12.8 15.4 11.3
4.0 X 10° 43.1 16.8 20.8 24.9 26.0 4.0 X 10° 30.5 23.8 8.32 16.8 19.8 15.5
5.0 X 10° 47.2 20.9 23.2 28.1 29.3 5.0 X 10° 35.6 28.2 10.5 20.6 23.6 19.4
6.0 X 10° 51.0 24.6 25.2 31.2 31.7 6.0 X 10° 40.0 32.0 12.6 24.5 27.0 22.6
7.0 X 10° 54.6 28.2 27.1 34.2 33.9 7.0 X 10° 43.9 35.6 14.7 28.2 30.2 25.4
8.0 X 10° 58.0 31.5 28.8 37.2 36.2 8.0 X 10° 47.4 38.9 16.7 31.7 33.2 28.0
9.0 X 10° 61.1 34.5 30.3 40.0 38.3 9.0 X 10° 50.5 42.1 18.5 35.0 36.0 30.4
1.0 X 10 1 63.9 37.4 31.8 42.5 40.6 1.0 X 10 1 53.3 45.1 20.3 38.0 38.7 32.5
1.2 X 10 1 68.3 42.2 34.6 46.6 45.9 1.2 X 10 1 58.1 50.6 23.4 43.8 43.4 35.7
1.4 X 10 1 71.4 46.3 37.2 49.6 50.4 1.4 X 10 1 62.1 55.3 26.1 48.2 47.5 38.6
1.5 X 10 1 72.5 48.1 38.5 50.8 52.3 1.5 X 10 1 63.8 57.4 27.4 50.0 49.2 40.1
1.6 X 10 1 73.3 49.7 39.7 51.7 53.8 1.6 X 10 1 65.4 59.3 28.6 51.4 50.8 41.6
1.8 X 101 74.5 52.6 42.2 53.0 56.0 1.8 X 10 1 68.2 62.8 30.9 53.4 53.7 44.7
2.0 X 10 1 75.1 55.2 44.7 53.9 57.0 2.0 X 10 1 70.7 65.7 33.0 54.4 56.1 48.1
3.0 X 10 1 74.3 64.4 37.3 54.9 naa 3.0 X 10 1 79.2 76.4 42.1 naa 63.9 naa
<Xl
5.0 X 10 1 68.1 74.8 32.0 53.4 na 5.0 X 10 1 87.8 87.7 56.0 na 72.8 na 0">
0">
7.5 X 10 1 61.3 83.3 31.4 52.4 na 7.5 X 10 1 92.9 95.1 70.1 na 80.8 na ......
na 1.0 X 102 95.4 99.4 82.7 na 88.2 na ~
1.0 X 102 56.3 89.7 32.7 52.9 10
1.3 X 102 52.9 95.0 35.2 54.5 na 1.3 X 102 96.7 102 94.6 na 95.4 na t:0
1.5 X 102 50.7 99.7 38.6 56.9 na 1.5 X 102 97.3 104 106 na 103 na 0.
Q)
1.8 X 102 49.0 105 43.6 60.5 na 1.8 X 102 97.5 106 120 na 112 na ~

a Not available. a Not available. ~


U
......

113
TABLE A31- Gonads, female (ovaries) absorbed dose per unit TABLE A32 - Gonads, male (testes) absorbed dose per unit
neutron (luence, DT I cP, in units ofpGy cm2 for monoenergetic neutron (luence, DT I cP, in units ofpGy cm2 for monoenergetic
neutrons incident in various geometries on an adult neutrons incident in various geometries on an adult
anthropomorphic computational model. These data are presented anthropomorphic computational model. These data are presented
graphically in Fig. A.25 (Annex 1) graphically in Fig. A.26 (Annex 1)
Energy Energy
(MeV) AP PA LAT ROT ISO (MeV) AP PA LAT ROT ISO

1.0 X 10- 9 0.75 0.80 0.20 0.50 0.38 1.0 X 10- 9 2.00 0.36 0.15 0.68 0.65
1.0 X 10- 8 1.00 0.95 0.26 0.72 0.43 1.0 X 10- 8 2.50 0.47 0.19 0.83 0.75
2.5 X 10- 8 1.19 1.16 0.30 0.88 0.51 2.5 X 10- 8 2.75 0.55 0.22 0.97 0.81
1.0 X 10- 7 1.60 1.63 0.43 1.13 0 .69 1.0 X 10- 7 3.31 0 .70 0.27 1.24 0.99
2.0 X 10- 7 1.82 1.88 0.49 1.25 0.79 2.0 X 10- 7 3.59 0.78 0.31 1.36 1.09
5.0 X 10- 7 2.10 2.23 0.56 1.41 0.92 5.0 X 10- 7 3.91 0.89 0.35 1.50 1.20
1.0 X 10- 6 2.29 2.47 0.61 1.51 1.01 1.0 X 10- 6 4.10 0.96 0.38 1.59 1.27
2.0 X 10- 6 2.45 2.65 0.66 1.61 1.10 2.0 X 10- 6 4.22 1.03 0.41 1.65 1.31
5.0 X 10- 6 2.61 2.80 0.72 1.73 1.19 5.0 X 10- 6 4.27 1.12 0.43 1.69 1.34
1.0 X 10- 5 2.69 2.85 0.75 1.79 1.24 1.0 X 10- 5 4.22 1.17 0.44 1.69 1.33
2.0 X 10- 5 2.75 2.87 0.78 1.85 1.28 2.0 X 10- 5 4.13 1.21 0.45 1.64 1.30
5.0 X 10- 5 2.79 2.84 0.81 1.89 1.31 5.0 X 10- 5 3.95 1.25 0.46 1.57 1.25

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


1.0 X 10- 4 2.81 2.80 0.82 1.89 1.32 1.0 X 10- 4 3.81 1.25 0.46 1.51 1.20
2.0 X 10- 4 2.82 2.77 0.81 1.88 1.30 2.0 X 10- 4 3.66 1.24 0.46 1.46 1.15
5.0 X 10- 4 2.84 2.73 0.80 1.84 1.27 5.0 X 10- 4 3.50 1.21 0.45 1.41 1.10
1.0 X 10- 3 2.86 2.71 0.78 1.80 1.25 1.0 X 10- 3 3.42 1.18 0.44 1.39 1.06
2.0 X 10- 3 2.88 2.68 0 .77 1.77 1.24 2.0 X 10- 3 3.41 1.16 0.43 1.37 1.05
5.0 X 10- 3 2.91 2.68 0.76 1.76 1.25 5.0 X 10- 3 3.51 1.15 0.42 1.39 1.07
1.0 X 10- 2 2.94 2.70 0.77 1.78 1.28 1.0 X 10- 2 3.69 1.15 0.43 1.45 1.12
2.0 X 10- 2 2.97 2.72 0.79 1.83 1.33 2.0 X 10- 2 4.00 1.14 0.43 1.54 1.22
3.0 X 10- 2 2.99 2.76 0.81 1.88 1.37 3.0 X 10- 2 4.25 1.15 0.44 1.64 1.30
5.0 X 10- 2 3.04 2.85 0.84 1.97 1.44 5.0 X 10- 2 4.80 1.18 0.45 1.83 1.47
7.0 X 10- 2 3.09 2.95 0.87 2.04 1.49 7.0 X 10- 2 5.44 1.21 0.47 2.00 1.66
1.0 X 10- 1 3.17 3.10 0.91 2.14 1.55 1.0 X 10- 1 6.48 1.25 0.49 2.25 1.97
1.5 X 10- 1 3.32 3.22 0.97 2.27 1.63 1.5 X 10- 1 8.25 1.29 0.51 2.77 2.50
2.0 X 10- 1 3.46 3.38 1.02 2.38 1.70 2.0 X 10- 1 9.97 1.34 0.53 3.25 3.00
3.0 X 10- 1 3.74 3.77 1.12 2.57 1.82 3.0 X 10- 1 13.1 1.45 0.59 4.17 3.93
5.0 X 10- 1 4.54 4.70 1.30 2.90 2 .10 5.0 X 10- 1 18.4 1.70 0.73 5.83 5.57
7.0 X 10- 1 5.70 5.74 1.44 3.27 2.47 7.0 X 10- 1 22.4 1.95 0.85 7.34 7.02
9.0 X 10- 1 7.08 6.98 1.66 3 .93 2.89 9.0 X 10- 1 25.7 2.24 1.03 8.75 8.34
1.0 X 10° 7.81 7.67 1.81 4.38 3.12 1.0 X 100 27.1 2.41 1.15 9.42 8.96
1.2 X 10° 9.33 9.22 2.26 5.45 3.73 1.2 X 100 29.6 3.02 1.55 10.7 10.1
2.0 X 10° 15.5 15.7 4.85 10.8 6.78 2.0 X 10° 36.7 6.43 4.22 15.3 14.1
3.0 X 10° 22.8 23.2 8.44 17.1 11.3 3.0 X 100 42.7 11.9 8.03 20.2 18.2
4.0 X 10° 29.2 29.6 11.9 22.4 16.0 4.0 X 100 47.4 17.3 11.6 24.5 21.7
5.0 X 100 34.6 35.0 15.1 27.0 21.0 5.0 X 100 51. 7 21.5 14.8 28.2 24.8
6.0 X 10° 39.4 39.6 18.1 30.9 23.9 6.0 X 100 55.8 25.4 17.9 31.5 27.6
7.0 X 10° 43.6 43.5 20.8 34.3 27.0 7.0 X 100 59.7 29.1 20.7 34.5 30.2
8.0 X 10° 47.4 46.9 23.3 37.3 29.7 8.0 X 10° 63.3 32.7 23.3 37.2 32.7
9.0 X 10° 50.8 49.9 25.6 39.9 32.2 9.0 X 100 66.7 36.0 25.7 39.7 35.1
1.0 X 10 1 53.7 52.7 27.7 42.3 34.5 1.0 X 10 1 69.6 39.3 27.9 42.0 37.4
1.2 X 10 1 58.7 58.1 31.6 46.5 38.4 1.2 X 10 1 74.3 45.4 31.9 46.1 41.9
1.4 X 10 1 62.5 63.0 35.2 50.1 41.6 1.4 X 10 1 77.4 50.5 35.3 49.6 46.4
1.5 X 10 1 64.1 65.3 36.8 51.8 43.0 1.5 X 10 1 78.5 52.6 36.9 51.2 48.7
1.6 X 10 1 65.5 67.5 38.4 53.3 44.3 1.6 X 10 1 79.3 54.4 38.3 52.6 50.8
1.8 X 10 1 67.8 71.5 41.5 56.1 46.5 1.8 X 10 1 80.1 57.6 41.0 55.3 52.8
2.0 X 10 1 69.6 75.0 44.4 58.7 48.4 2.0 X 10 1 80.4 60.1 43.5 57.7 53.5
3.0 X 10 1 75.7 83.6 54.8 68.8 na a 3.0 X 10 1 77.7 68.7 53.1 62.8 naa
5.0 X 10 1 82.7 89.0 70.3 81.7 na 5.0 X 10 1 69.0 78.7 65.2 69.7 na
7.5 X 10 1 89.7 90.0 84.4 91.9 na 7.5 X 10 1 61.3 88.7 76.1 76.5 na
1.0 X 102 96.6 91.0 95.4 99.0 na 1.0 X 102 57.1 98.2 85.4 82.7 na
1.3 X 102 103 91.5 105 104 na 1.3 X 102 55.1 107 94.1 88.7 na
1.5 X 102 110 91.8 112 109 na 1.5 X 102 54.8 116 103 94.7 na
1.8 X 102 118 92.0 121 113 na 1.8 X 102 55.9 127 113 102 na
a Not available. a Not available.

114
<IJ
TABLE A.33 -Gonads (mean of ovaries and testes), absorbed dose TABLEA.34-Liver absorbed dose per unit neutron {luence, DT / <1>,
per unit neutron {luence, DT / $, in units ofpGy cm2 for in units of pGy cm2 for monoenergetic neutrons incident in ~
monoenergetic neutrons incident in various geometries on an various geometries on an adult anthropomorphic computational ~
adult anthropomorphic computational model. These data are model. These data are presented graphically in C'i
><
presented graphically in Fig. A.27 (Annex 1) Fig. A.28 (Annex 1) QI
~

Energy Energy ~
(MeV) AP PA LAT ROT ISO (MeV) AP PA RLAT LLAT ROT ISO

1.0 X 10- 9 1.38 0.58 0.19 0.59 0.51 1.0 X 10- 9 0.98 0.70 0.60 0.11 0.61 0.46
1.0 X 10- 8 1.75 0 .71 0.23 0.78 0.59 1.0 X 10- 8 1.20 0.92 0.71 0.12 0.71 0.56
2.5 X 10- 8 1.97 0.85 0.26 0.93 0.66 2.5 X 10-8 1.45 1.10 0.85 0.14 0.86 0.66
1.0 X 10- 7 2.46 1.17 0.35 1.18 0.84 1.0 X 10- 7 2.06 1.46 1.13 0.18 1.20 0.86
2.0 X 10- 7 2.70 1.33 0.40 1.31 0.94 2.0 X 10- 7 2.36 1.65 1.30 0.20 1.37 0.97
5.0 X 10- 7 3.01 1.56 0.46 1.45 1.06 5.0 X 10- 7 2.74 1.91 1.53 0.23 1.59 1.11
1.0 X 10- 6 3.20 1.72 0.50 1.55 1.14 1.0 X 10- 6 2.99 2.09 1.69 0.25 1.74 1.22
2.0 X 10- 6 3.34 1.84 0.53 1.63 1.20 2.0 X 10- 6 3.15 2.23 1.80 0.27 1.87 1.30
5.0 X 10- 6 3.44 1.96 0.57 1.71 1.26 5.0 X 10- 6 3.27 2.37 1.89 0.28 1.98 1.38
1.0 X 10- 5 3.46 2.01 0.60 1.74 1.28 1.0 X 10- 5 3.30 2.44 1.92 0.29 2.03 1.41
2.0 X 10- 5 3.44 2.04 0.61 1.75 1.29 2.0 X 10- 5 3.28 2.48 1.93 0.30 2.04 1.43

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


5.0 X 10- 5 3.37 2.04 0.63 1.73 1.28 5.0 X 10- 5 3.22 2.49 1.91 0.31 2.03 1.43
1.0 X 10- 4 3.31 2.03 0.64 1.70 1.26 1.0 X 10- 4 3.16 2.48 1.90 0.31 2.01 1.42
2.0 X 10- 4 3.24 2.00 0.63 1.67 1.23 2.0 X 10- 4 3.15 2.45 1.88 0.31 1.99 1.39
5.0 X 10- 4 3.17 1.97 0.62 1.63 1.18 5.0 X 10- 4 3.13 2.40 1.85 0.30 1.96 1.35
1.0 X 10-3 3.14 1.95 0.61 1.60 1.16 1.0 X 10- 3 3.13 2.36 1.83 0.30 1.95 1.33
2.0 X 10- 3 3.14 1.92 0.60 1.57 1.15 2.0 X 10- 3 3.10 2.34 1.80 0.30 1.94 1.31
5.0 X 10- 3 3.21 1.91 0.59 1.57 1.16 5.0 X 10- 3 3.08 2.32 1.77 0.29 1.94 1.30
1.0 X 10- 2 3.32 1.92 0.60 1.61 1.20 1.0 X 10- 2 3.08 2.34 1.78 0.30 1.96 1.32
2.0 X 10- 2 3.49 1.93 0.61 1.69 1.27 2.0 X 10- 2 3.06 2.32 1.76 0.31 1.94 1.35
3.0 X 10- 2 3.62 1.96 0.62 1.76 1.33 3.0 X 10- 2 3.09 2.33 1.79 0.32 1.95 1.39
5.0 X 10- 2 3.92 2.02 0.65 1.90 1.45 5.0 X 10- 2 3.18 2.41 1.86 0.33 2.02 1.47
7.0 X 10- 2 4.26 2.08 0.67 2.02 1.58 7.0 X 10- 2 3.30 2.50 1.95 0.35 2.10 1.54
1.0 X 10- 1 4.83 2.17 0.70 2.19 1.76 1.0 X 10- 1 3.51 2.64 2.09 0.36 2.24 1.64
1.5 X 10- 1 5.79 2.25 0.74 2.52 2.06 1.5 X 10- 1 3.99 2.85 2.29 0.38 2.45 1.74
2.0 X 10- 1 6.72 2.36 0.78 2.82 2.35 2.0 X 10- 1 4.47 3.08 2.51 0.39 2.67 1.85
3.0 X 10- 1 8.44 2.61 0.86 3.37 2.87 3.0 X 10- 1 5.56 3.55 2.97 0.42 3.19 2.08
5.0 X 10- 1 11.5 3.20 1.01 4.36 3.84 5.0 X 10- 1 7.69 4.59 4.01 0.46 4.29 2.66
7.0 X 10- 1 14.1 3.84 1.14 5.30 4.75 7.0 X 10- 1 9.75 5.77 5.24 0.49 5.45 3.50
9.0 X 10- 1 16.4 4.61 1.35 6.34 5.62 9.0 X 10- 1 11.7 6.99 6.52 0.58 6.68 4.41
1.0 X 10° 17.5 5.04 1.48 6.90 6.04 1.0 X 10° 12.7 7.62 7.19 0.63 7.30 4.89
1.2 X 10° 19.4 6.12 1.91 8.08 6.93 1.2 X 10° 14.6 9.00 8.59 0.79 8.57 5.85
2.0 X 10° 26.1 11.0 4.53 13.1 10.5 2.0 X 10° 21.4 14.7 14.4 1.84 13.6 9.78
3.0 X 10° 32.7 17.6 8.23 18.7 14.8 3.0 X 10° 28.6 21.3 21.2 3.42 19.4 14.6
4.0 X 10° 38.3 23.5 11.7 23.5 18.9 4.0 X 10° 34.6 26.9 26.6 5.21 24.5 18.9
5.0 X 10° 43.2 28.3 15.0 27.6 22.9 5.0 X 10° 39.7 31.4 31.3 7.11 29.0 22.8
6.0 X 10° 47.6 32.5 18.0 31.2 25.8 6.0 X 10° 44.2 35.4 35.2 8.99 32.9 25.5
7.0 X 10° 51.6 36.3 20.8 34.4 28.6 7.0 X 10° 48.2 39.1 38.7 10.9 36.4 28.0
8.0 X 10° 55.4 39.8 23.3 37.2 31.2 8.0 X 10° 51.8 42.4 41.7 12.7 39.6 30.4
9.0 X 10° 58.7 43.0 25.7 39.8 33.6 9.0 X 10° 55.0 45.4 44.5 14.4 42.4 32.7
1.0 X 10 1 61.7 46.0 27.8 42.2 35.9 1.0 X 10 1 57.8 48.3 47.0 16.2 44.9 34.9
1.2 X 10 1 66.5 51.8 31.8 46.3 40.1 1.2 X 10 1 62.4 53.3 51.3 19.4 49.0 39.7
1.4 X 10 1 70.0 56.8 35.2 49.8 44.0 1.4 X 101 66.0 57.4 55.1 22.3 52.5 43.8
1.5 X 10 1 71.3 58.9 36.8 51.5 45.8 1.5 X 10 1 67.5 59.1 56.7 23.7 54.0 45.5
1.6 X 10 1 72.4 61.0 38.4 53.0 47.5 1.6 X 10 1 68.7 60.6 58.2 25.0 55.5 47.0
1.8 X 101 74.0 64.5 41.3 55.7 49.7 1.8 X 10 1 70.8 63.1 61.0 27.4 58.1 49.2
2.0 X 10 1 75.0 67.6 44.0 58.2 51.0 2.0 X 10 1 72.4 65.2 63.4 29.5 60.4 50.6
3.0 X 10 1 76.7 76.1 53.9 65.8 naa 3.0 X 10 1 76.9 71 .7 71.7 na a 68.9 na a
00
5.0 X 10 1 75.8 83.9 67.8 75.7 na 5.0 X 10 1 80.1 78.1 80.4 na 78.5 na O"l
O"l
7.5 X 10 1 75.5 89.4 80.3 84.2 na 7.5 X 10 1 82.0 83.6 86.6 na 85.3 na .....
1.0 X 102 76.8 94.6 90.4 90.8 na 1.0 X 102 83.6 88.5 90.9 na 89.7 na t--"
LQ
1.3 X 102 79.3 99.4 99.3 96.5 na 1.3 X 102 85.3 93.2 94.3 na 92.8 na t0
1.5 X 102 82.5 104 107 102 na 1.5 X 102 87.2 97.8 97.3 na 95.1 na c..
QI
1.8 X 102 87.1 109 117 107 na 1.8 X 102 89.5 103 100 na 97.4 na p::
a Not available. a Not available. 0p::
U
.-.

115
~
0
T ABLE A.35 -Lung absorbed dose per unit neutron {luence, DT/ $, TABLE A.36 - Oesophagus absorbed dose per unit neutron {luence,
:.::l in units ofpGy cm2 for monoenergetic neutrons incident in D T/ $ , in units of pGy cm 2 for monoenergetic neutrons incident in
;a'" various geometries on an adult anthropomorphic computational various geometries on an adult anthropomorphic computational
'"
p:::
OJ
model. These data are presented graphically in
Fig. A.29 (Annex 1)
model. These data are presented graphically in
Fig. A.30 (Annex 1)
e
Ol Energy Energy
"t< (MeV) AP PA LAT ROT ISO (MeV) AP PA LAT ROT ISO
""
;.>
00
~ 1.0 X 10- 9 0.77 0.81 0.33 0.58 0.47 1.0 X 10- 9 0.50 0.95 0.30 0.53 0.40
'@ 1.0 X 10- 8 0.95 1.05 0.42 0.72 0.55 1.0 X 10- 8 0.73 1.13 0.37 0.64 0.48
bO
...: 2.5 X 10- 8 1.11 1.27 0.49 0.86 0.63 2.5 X 10- 8 0.88 1.30 0.42 0.77 0.56
~
0 1.0 X 10- 7 1.52 1.67 0.63 1.13 0.81 1.0 X 10- 7 1.24 1.79 0.52 1.05 0.75
:.::l 2.0 X 10- 7 1.74 1.89 0.71 1.27 0.92 2.0 X 10- 7 1.43 2.04 0.59 1.20 0.86
C.l
Ol
;.> 5.0 X 10- 7 2.03 2.18 0.81 1.44 1.05 5.0 X 10- 7 1.69 2.37 0.68 1.38 0.99
...
0
p.. 1.0 X 10- 6 2.21 2.38 0.88 1.56 1.15 1.0 X 10- 6 1.87 2.59 0.76 1.51 1.09
OJC.l 2.0 X 10- 6 2.32 2.53 0.94 1.65 1.22 2.0 X 10- 6 2.00 2.76 0.81 1.62 1.17
'So 5.0 X 10- 6 2.39 2.59 0.99 1.74 1.28 5.0 X 10- 6 2.13 2.94 0.88 1.73 1.26
0 1.0 X 10- 5
'0 1.0 X 10- 5 2.40 2.60 1.01 1.78 1.31 2.19 3.03 0.91 1.79 1.31
;a 2.0 X 10- 5 2.39 2.59 1.03 1.80 1.32 2.0 X 10- 5 2.22 3.08 0.93 1.81 1.34
'"
p::: 5.0
1.0
X 10- 5
10- 4
2.36 2.55
2.52
1.03
1.02
1.79 1.31
1.30
5.0 X
1.0 X
10- 5
10- 4
2.24
2.24
3.12
3.12
0.94
0.94
1.83
1.82
1.36
1.36
.S 2.34 1.77

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


X
Ol
00 2.0 X 10- 4 2.34 2.51 1.01 1.75 1.27 2.0 X 10- 4 2.26 3.12 0.95 1.82 1.34
;j
... 5.0 X 10- 4
10- 3
2.33 2.50 1.00 1.70 1.25 5.0 X
1.0 X
10- 4
10- 3
2.28 3.11 0.94 1.82 1.31
<£ 1.0 X 2.33 2.50 0.98 1.68 1.23 2.31 3.09 0.94 1.81 1.29
00
;.> 2.0 X 10- 3 2.32 2.49 0.97 1.65 1.21 2.0 X 10- 3 2.35 3.05 0.94 1.81 1.29
~
Ol 5.0 X 10- 3 2.31 2.49 0.95 1.63 1.20 5.0 X 10- 3 2.41 3.02 0.95 1.82 1.29
'f:)
!EOl 1.0 X 10- 2 2.31 2.50 0.96 1.65 1.22 1.0 X 10- 2 2.45 3.01 0.96 1.84 1.32
0 2.0 X 10- 2 2.31 2.46 0.95 1.62 1.23 2.0 X 10- 2 2.47 2.96 0.95 1.86 1.31
Co) 10- 2
3.0 X 10- 2 2.32 2.47 0.96 1.64 1.26 3.0 X 2.49 2.97 0.96 1.88 1.33
~
0 5.0 X 10- 2 2.38 2.58 1.00 1.72 1.32 5.0 X 10- 2 2.52 3.03 0.98 1.93 1.37
'00
...
Ol
7.0 X 10- 2 2.46 2.71 1.05 1.83 1.39 7.0 X 10- 2 2.55 3.11 1.02 1.97 1.42
> 1.0 X 10- 1 2.62 3.00 1.13 1.99 1.51 1.0 X 10- 1 2.63 3.25 1.07 2.03 1.49
~
0
Co)
1.5 X 10- 1 3.06 3.68 1.26 2.29 1.68 1.5 X 10- 1 2.70 3.42 1.13 2.09 1.58
2.0 X 10- 1 3.49 4.30 1.39 2.60 1.86 2.0 X 10- 1 2.82 3.62 1.20 2.18 1.67
3.0 X 10- 1 4.43 5.43 1.67 3.24 2.22 3.0 X 10- 1 3.14 4.08 1.36 2.39 1.85
5.0 X 10- 1 6.28 7.70 2.26 4.57 3.06 5.0 X 10- 1 4.06 5.11 1.72 2.89 2.25
7.0 X 10- 1 8.21 9.97 2.92 5.98 4.09 7.0 X 10- 1 5.34 6.35 2.09 3.50 2.68
9.0 X 10- 1 10.1 12.2 3.64 7.38 5.21 9.0 X 10- 1 6.83 7.60 2.53 4.33 3.13
1.0 X 10° 11.1 13.3 4.04 8.08 5.78 1.0 X 10° 7.65 8.23 2.77 4.81 3.38
1.2 X 10° 12.9 15.5 4.96 9.51 6.94 1.2 X 10° 9.45 9.46 3.41 5.87 4.14
2.0 X 10° 19.7 23.6 9.12 15.0 11.5 2.0 X 10° 16.0 14.2 6.59 10.5 7.59
3.0 X 10° 27.1 31.8 13.9 21.3 16.8 3.0 X 10° 23.7 19.7 11.1 16.6 12.2
4.0 X 10° 33.1 38.0 18.0 26.6 21.4 4.0 X 10° 30.0 24.7 15.3 22.2 16.7
5.0 X 10° 38.2 43.1 21.5 31.2 25.2 5.0 X 10° 35.2 29.4 19.3 26.9 20.7
6.0 X 10° 42.6 47.3 24.6 35.0 28.2 6.0 X 10° 39.6 33.7 23.0 31.2 23.4
7.0 X 10° 46.4 50.9 27.4 38.3 30.8 7.0 X 10° 43.2 37.8 26.4 34.9 25.9
8.0 X 10° 49.7 54.1 29.9 41.4 33.1 8.0 X 10° 46.3 41.5 29.6 38.3 28.2
9.0 X 10° 52.7 57.0 32.2 44.1 35.3 9.0 X 10° 49.0 44.9 32.5 41.3 30.5
1.0 X 101 55.3 59.7 34.3 46.7 37.4 1.0 X 101 51.3 48.1 35.3 44.0 32.7
1.2 X 101 59.7 64.3 38.2 50.9 41.9 1.2 X 101 55.1 53.5 40.3 48.6 37.7
1.4 X 101 63.3 67.9 41.5 54.5 45.9 1.4 X 101 58.0 57.9 44.3 52.3 41.9
1.5 X 101 64.8 69.5 43.0 56.1 47.8 1.5 X 101 59.2 59.7 46.0 53.9 43.7
1.6 X 101 66.2 70.8 44.5 57.5 49.4 1.6 X 101 60.3 61.3 47.5 55.4 45.2
1.8 X 101 68.5 73.1 47.1 60.0 51.8 1.8 X 101 62.2 64.0 50.1 58.0 47.5
2.0 X 10 1 70.5 74.9 49.5 62.1 52.4 2.0 X 101 63.7 66.2 52.2 60.3 48.8
3.0 X 101 77.0 80.3 58.3 69.2 naa 3.0 X 101 69.2 73.0 62.3 67.8 naa
00
en 5.0 X 101 83.1 83.9 69.6 76.7 na 5.0 X 101 76.9 79.5 74.0 76.5 na
en
..... 7.5 X 101 86.4 85.2 79.1 82.2 na 7.5 X 101 85.3 85.0 83.1 84.1 na
[--"
1.0 X 102 88.1 85.4 86.7 86.4 na 1.0 X 102 93.5 90.0 90.3 90.8 na
>0
~ 1.3 X 102 89.1 85.5 93.2 90.0 na 1.3 X 102 101 94.8 96.7 97.2 na
0
P- 1.5 X 102 89.7 85.5 99.3 93.3 na 1.5 X 102 109 99.6 103 103 na
Ol
p::: 1.8 X 102 90.2 85.5 106 97.1 na 1.8 X 102 118 105 110 111 na
:;J
p::: a Not available. a Not available.

-
Co)

116
TABLE A.37 - Remainder absorbed dose per unit neutron fluence, TABLE A.38 - Skin absorbed dose per unit neutron fluence, DT / <1>, '"
~

~
DT / <1>, in units ofpGy cm2 for monoenergetic neutrons incident in in units ofpGy cm2 for monoenergetic neutrons incident in
various geometries on an adult anthropomorphic computational various geometries on an adult anthropomorphic computational
model. These data are presented graphically in model. These data are presented graphically in C\i
~
Fig. A.31 (Annex 1) Fig. A.32 (Annex 1) ~
I'i
Energy Energy ~
(MeV) AP PA LAT ROT ISO (MeV) AP PA LAT ROT ISO

1.0 X 10- 9 0.80 0.85 0.29 0.57 0.44 1.0 X 10- 9 1.35 1.30 0.66 1.00 0.82
1.0 X 10- 8 1.00 1.11 0.43 0.72 0.57 1.0 X 10- 8 1.38 1.34 0.68 1.02 0.83
2.5 X 10- 8 1.20 1.27 0.53 0.88 0.67 2.5 X 10- 8 1.43 1.40 0.70 1.06 0.84
1.0 X 10- 7 1.59 1.64 0.71 1.18 0.86 1.0 X 10- 7 1.54 1.51 0.73 1.15 0.86
2.0 X 10- 7 1.79 1.84 0.79 1.34 0.95 2.0 X 10- 7 1.61 1.58 0.75 1.19 0.87
5.0 X 10- 7 2.05 2.09 0.90 1.53 1.07 5.0 X 10- 7 1.68 1.66 0.77 1.24 0.89
1.0 X 10- 6 2.21 2.26 0.96 1.65 1.14 1.0 X 10- 6 1.72 1.71 0.78 1.27 0.90
2.0 X 10- 6 2.33 2.40 1.01 1.74 1.21 2.0 X 10- 6 1.75 1.74 0.78 1.29 0.91
5.0 X 10- 6 2.43 2.54 1.05 1.80 1.27 5.0 X 10- 6 1.76 1.75 0.78 1.29 0.92
1.0 X 10- 5 2.45 2.61 1.07 1.82 1.29 1.0 X 10- 5 1.75 1.74 0.77 1.28 0.92
2.0 X 10- 5 2.45 2.64 1.07 1.80 1.30 2.0 X 10- 5 1.72 1.71 0.75 1.26 0.91

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


5.0 X 10- 5 2.42 2.64 1.05 1.77 1.30 5.0 X 10- 5 1.67 1.66 0.73 1.22 0.89
1.0 X 10- 4 2.38 2.62 1.04 1.73 1.28 1.0 X 10- 4 1.62 1.61 0.71 1.18 0.87
2.0 X 10- 4 2.33 2.55 1.01 1.70 1.24 2.0 X 10- 4 1.56 1.55 0.68 1.12 0.83
5.0 X 10- 4 2.29 2.47 0.97 1.67 1.18 5.0 X 10- 4 1.49 1.48 0.66 1.06 0.79
1.0 X 10- 3 2.27 2.42 0.95 1.66 1.15 1.0 X 10- 3 1.46 1.45 0.66 1.06 0.79
2.0 X 10- 3 2.27 2.39 0.93 1.67 1.13 2.0 X 10- 3 1.48 1.48 0.69 1.11 0.82
5.0 X 10- 3 2.31 2.41 0.94 1.70 1.14 5.0 X 10- 3 1.66 1.65 0.80 1.27 0.93
1.0 X 10- 2 2.37 2.48 0.97 1.74 1.18 1.0 X 10- 2 1.94 1.93 0.98 1.50 1.10
2.0 X 10- 2 2.46 2.61 1.03 1.80 1.24 2.0 X 10- 2 2.38 2.38 1.31 1.89 1.52
3.0 X 10- 2 2.53 2.73 1.08 1.84 1.31 3.0 X 10- 2 2.73 2.72 1.59 2.22 1.87
5.0 X 10- 2 2.67 2.95 1.19 1.92 1.44 5.0 X 10- 2 3.35 3.34 2.08 2.79 2.48
7.0 X 10- 2 2.84 3.17 1.29 2.03 1.56 7.0 X 10- 2 3.92 3.90 2.52 3.30 3.02
1.0 X 10- 1 3.10 3.48 1.43 2.20 1.72 1.0 X 10- 1 4.72 4.70 3.11 3.99 3.74
1.5 X 10- 1 3.53 3.94 1.65 2.51 1.97 1.5 X 10- 1 5.94 5.92 4.02 5.11 4.78
2.0 X 10- 1 3.94 4.39 1.85 2.81 2.20 2.0 X 10- 1 7.03 7.01 4.84 6.13 5.69
3.0 X 10- 1 4.71 5.23 2.22 3.38 2.66 3.0 X 10- 1 8.95 8.93 6.29 7.89 7.24
5.0 X 10- 1 6.23 6.88 3.00 4.57 3.53 5.0 X 10- 1 12.0 12.0 8.67 10.8 9.78
7.0 X 10- 1 7.82 8.60 3.89 5.88 4.37 7.0 X 10- 1 14.5 14.4 10.6 13.1 11.9
9.0 X 10- 1 9.43 10.3 4.83 7.25 5.21 9.0 X 10- 1 16.5 16.5 12.3 15.1 13.7
1.0 X 10° 10.2 11.1 5.31 7.94 5.63 1.0 X 10° 17.4 17.3 13.1 15.9 14.5
1.2 X 10° 11.8 12.9 6.30 9.33 6.71 1.2 X 10° 19.0 18.9 14.5 17.4 16.0
2.0 X 10° 17.8 19.6 10.3 14.6 11.1 2.0 X 10° 23.9 23.9 19.0 22.2 20.7
3.0 X 10° 24.3 26.8 14.9 20.6 16.3 3.0 X 10° 28.5 28.4 23.5 26.7 25.3
4.0 X 10° 29.9 32.8 19.0 25.7 21.0 4.0 X 10° 32.5 32.4 27.4 30.6 29.0
5.0 X 10° 34.7 37.7 22.6 30.0 25.1 5.0 X 10° 36.4 36.3 30.9 34.6 32.2
6.0 X 10° 38.9 41.8 25.6 33.9 28.0 6.0 X 10° 40.2 40.1 34.1 38.3 34.9
7.0 X 10° 42.7 45.4 28.4 37.3 30.6 7.0 X 10° 43.9 43.8 37.1 41.7 37.3
8.0 X 10° 46.1 48.6 30.8 40.4 33.0 8.0 X 10° 47.4 47.4 39.8 44.9 39.7
9.0 X 10° 49.1 51.5 33.1 43.1 35.3 9.0 X 10° 50.7 50.7 42.3 47.8 41.9
1.0 X 101 51.8 54.1 35.2 45.6 37.5 1.0 X 10 1 53.6 53.6 44.5 50.3 44.1
1.2 X 10 1 56.5 58.7 39.0 49.8 41.9 1.2 X 10 1 58.2 58.2 48.3 54.2 48.5
1.4 X 10 1 60.4 62.4 42.5 53.3 45.9 1.4 X 10 1 61.2 61.3 51.4 57.0 52.5
1.5 X 10 1 62.1 63.9 44.1 54.8 47.8 1.5 X 10 1 62.3 62.4 52.7 58.0 54.3
1.6 X 10 1 63.6 65.3 45.7 56.2 49.6 1.6 X 10 1 63.0 63.1 53.9 58.9 56.0
1.8 X 10 1 66.3 67.7 48.4 58.6 52.1 1.8 X 10 1 63.8 63.9 56.0 60.1 58.3
2.0 X 10 1 68.6 69.7 50.5 60.7 53.0 2.0 X 10 1 64.1 64.1 57.7 60.8 59.0
3.0 X 10 1 76.6 76.5 58.2 68.4 naa 3.0 X 10 1 61.6 61.6 57.0 57.5 naa
r:L)
5.0 X 10 1 85.3 83.9 70.6 77.9 na 5.0 X 10 1 55.1 54.9 55.4 53.1 na O"l
O"l
7.5 X 10 1 91.3 89.8 81.9 86.3 na 7.5 X 10 1 51.5 51.2 55.1 52.3 na .....
1.0 X 102 95.3 94.6 91.3 93.1 na 1.0 X 102 51.8 51.5 56.8 54.1 na r:-"
>t:>
1.3 X 102 98.4 98.9 99.6 99.1 na 1.3 X 102 54.7 54.4 59.8 57.3 na t:0
1.5 X 102 101 103 107 105 na 1.5 X 102 59.1 59.0 63.8 61.6 na 0.
1.8 X 102 103 107 116 111 na 1.8 X 102 65.7 65.8 69.5 67.8 na ~
p::
a Not available. Not available. ~
a p::
....
U

117
s::0 TABLE A.39-Stomach absorbed dose per unit neutron flu ence, TABLE A.40- Thyroid absorbed dose per unit neutron fluence ,
:;3
OJ
DT / <P, in units of pGy cm2 for monoenergetic neutrons incident in DT / <P, in units ofpGy cm 2 for monoenergetic neutrons incident in
;a various geometries on an adult anthropomorphic computational various geometries on an adult anthropomorphic computational
OJ
~ model. These data are presented graphically in model. These data are presented graphically in
til Fig. A.33 (Annex 1) Fig. A.34 (Annex 1)
E
.2S~ Energy Energy
(MeV) AP PA RLAT LLAT ROT ISO (MeV) AP PA LAT ROT ISO
ril
...,
.~
'"s:: 1.0 X 10- 9 1.23 0.50 0.11 0.49 0.59 0.45 1.0 X 10- 9 1.41 0.29 0.51 0.74 0.59
bIl
1.0 X 10- 8 1.60 0.64 0.14 0.55 0.73 0.58 1.0 X 10- 8 1.77 0.36 0.58 0.81 0.64
<s:: 2.5 X 10- 8 1.90 0.77 0.16 0.60 0.87 0.67 2.5 X 10- 8 1.99 0.41 0.64 0.90 0.69
0 1.0 X 10- 7 2.59 1.03 0.21 0.72 1.17 0.84 1.0 X 10- 7 2.37 0.51 0.76 1.10 0.77
:;3
<..> 2.0 X 10- 7 2.97 1.16 0.23 0.82 1.32 0.93 2.0 X 10- 7 2.56 0.56 0.86 1.22 0.84
.2S
0 5.0 X 10- 7 3.46 1.35 0.27 0.99 1.51 1.06 5.0 X 10- 7 2.78 0.63 1.01 1.39 0.93
I-<
p.. 1.0 X 10- 6 3.78 1.48 0.29 1.13 1.64 1.15 1.0 X 10- 6 2.91 0.69 1.12 1.50 1.00
til<..> 2.0 X 10- 6 4.01 1.59 0.31 1.21 1.75 1.23 2.0 X 10- 6 3.00 0.75 1.18 1.57 1.05
.6b 5.0 X 10- 6 4.17 1.71 0.33 1.29 1.86 1.31 5.0 X 10- 6 3.04 0.82 1.23 1.62 1.11
0
'0 1.0 X 10- 5 4.20 1.77 0.34 1.32 1.91 1.35 1.0 X 10- 5 3.02 0.87 1.24 1.63 1.14
;a 2.0 X 10- 5 4.17 1.82 0.35 1.33 1.91 1.38 2.0 X 10- 5 2.97 0.91 1.24 1.61 1.15
OJ
~ 5.0 X 10- 5 4.08 1.85 0.35 1.34 1.89 1.40 5.0 X 10- 5 2.88 0.95 1.24 1.57 1.15

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


.S 1.0 X 10- 4 4.00 1.85 0.35 1.34 1.86 1.39 1.0 X 10- 4 2.80 0.97 1.24 1.54 1.14
Q)
2.0 X 10- 4 3.95 1.83 0.35 1.34 1.84 1.37 2.0 X 10- 4 2.74 0.98 1.23 1.52 1.11
'"::l 5.0 X 10- 4 3.91 1.80 0.34 1.35 1.82 1.33 5.0 X 10- 4 2.67 0.98 1.22 1.49 1.07
I-<
..s 1.0 X 10- 3 3.91 1.77 0.34 1.35 1.80 1.31 1.0 X 10- 3 2.66 0.98 1.21 1.49 1.04
..,'" 2.0 X 10- 3 3.92 1.76 0.34 1.35 1.78 1.28 2.0 X 10- 3 2.67 0.97 1.20 1.46 1.01
s::
Q)
.<) 5.0 X 10- 3 3.90 1.76 0.34 1.36 1.77 1.27 5.0 X 10- 3 2.74 0.96 1.20 1.47 1.01
!E 1.0 X 10- 2 3.87 1.77 0.34 1.38 1.79 1.29 1.0 X 10- 2 2.85 0.96 1.23 1.52 1.04
Q)
0 2.0 X 10- 2 3.87 1.79 0.34 1.38 1.79 1.32 2.0 X 10- 2 3.00 0.96 1.24 1.62 1.11
U 3.0 X 10- 2 3.85 1.81 0.34 1.39 1.82 1.36 3.0 X 10- 2 3.11 0.97 1.28 1.70 1.17
s::0
5.0 X 10- 2 3.94 1.86 0.35 1.44 1.90 1.43 5.0 X 10- 2 3.44 0.99 1.38 1.88 1.30
·fii
I-<
Q)
7.0 X 10- 2 4.05 1.91 0.36 1.50 1.99 1.51 7.0 X 10- 2 3.89 0.99 1.49 2.07 1.42
s::0> 1.0 X 10- 1 4.32 1.98 0.37 1.60 2.13 1.61 1.0 X 10- 1 4.68 1.01 1.67 2.35 1.59
1.5 X 10- 1 5.09 2.07 0.38 1.73 2.34 1.72 1.5 X 10- 1 6.10 1.04 2.04 2.90 1.89
u
2.0 X 10- 1 5.85 2.17 0.39 1.87 2.55 1.85 2.0 X 10- 1 7.52 1.08 2.43 3.44 2.17
3.0 X 10- 1 7.39 2.32 0.42 2.20 3.04 2.14 3.0 X 10- 1 10.2 1.17 3.22 4.51 2.72
5.0 X 10- 1 10.3 2.65 0.49 2.94 4.06 2.81 5.0 X 10- 1 14.7 1.37 4.91 6.55 3.74
7.0 X 10- 1 12.9 2.95 0.54 3.83 5.14 3.62 7.0 X 10- 1 18.3 1.59 6.80 8.48 4.69
9.0 X 10- 1 15.4 3.42 0.63 4.81 6.21 4.45 9.0 X 10- 1 21.3 1.93 8.62 10.3 5.60
1.0 X 10° 16.6 3.72 0.70 5.32 6.75 4.88 1.0 X 10° 22.6 2.14 9.51 11.2 6.05
1.2 X 10° 18.8 4.64 0.90 6.43 7.87 5.76 1.2 X 10° 24.9 2.70 11.1 12.8 6.97
2.0 X 10° 26.4 8.82 2.09 11.3 12.3 9.40 2.0 X 10° 32.1 5.67 17.2 18.7 10.5
3.0 X 10° 34.1 14.5 3.99 16.8 17.5 13.8 3.0 X 10° 38.2 10.2 23.7 24.9 14.7
4.0 X 10° 40.4 19.8 5.87 21.8 22.1 17.9 4.0 X 10° 43.1 14.0 29.2 30.1 18.5
5.0 X 10° 45.6 24.2 7.77 26.3 26.1 21.5 5.0 X 10° 47.3 17.5 34.1 34.6 22.0
6.0 X 10° 50.1 28.0 9.65 30.6 29.5 24.3 6.0 X 10° 51.2 20.6 38.5 38.7 24.9
7.0 X 10° 54.0 31.6 11.5 34.6 32.7 26.8 7.0 X 10° 54.7 23.3 42.4 42.3 27.7
8.0 X 10° 57.4 34.8 13.3 38.2 35.7 29.2 8.0 X 10° 58.0 25.7 46.0 45.5 30.4
9.0 X 10° 60.5 37.8 15.1 41.5 38.5 31.4 9.0 X 10° 61.0 27.8 49.2 48.4 33.2
1.0 X 10 1 63.2 40.5 16.8 44.5 41.2 33.6 1.0 X 10 1 63.7 29.7 52.1 51.0 36.0
1.2 X 10 1 67.8 45.4 20.1 49.7 46.1 38.1 1.2 X 10 1 68.1 33.3 57.2 55.5 41.4
1.4 X 10 1 71.4 49.5 23.1 53.9 50.2 42.0 1.4 X 10 1 71.4 36.7 61.3 59.3 47.5
1.5 X 10 1 72.9 51.4 24.6 55.6 51.9 43.7 1.5 X 10 1 72.7 38.4 63.1 61.0 50.9
1.6 X 101 74.3 53.0 26.0 57.1 53.5 45.2 1.6 X 10 1 73.8 40.1 64.7 62.5 54.6
1.8 X 101 76.5 56.0 28.7 59.7 56.2 47.7 1.8 X 10 1 75.5 43.3 67.4 65.4 58.2
2.0 X 10 1 78.4 58.6 31.2 61.7 58.5 49.5 2.0 X 10 1 76.7 46.5 69.6 67.9 57.0
3.0 X 10 1 84.1 68.5 41.9 na· 65.6 na' 3.0 X 10 1 78.9 60.6 79.3 76.3 na'
CO
5.0 X 10 1 87.7 81.1 58.2 na 73.6 na 5.0 X 10 1 77.3 81.8 88.1 84.4 na
'"'"
..-<
too"
7.5 X
1.0 X
10 1
102
88.0
86.8
92.5
102
74.0
87.5
na
na
81.5
89.2
na
na
7.5 X 10 1
1.0 X 102
73.6
70.3
99.2
111
91.7
91.1
88.6
90.2
na
na
>t:l
1:0 1.3 X 102 85.1 110 99.9 na 97.1 na 1.3 X 102 67.5 120 88.8 90.8 na
Po 1.5 X 102 83.3 117 112 na 105 na 1.5 X 102 65.2 127 85.7 90.8 na
~ 1.8 X 102 81.0 125 125 na 115 na 1.8 X 102 63.0 133 81.7 90.3 na
~
~ , Not available. ' Not available.
U
......

118
TABLE A.41-Effective dose per unit neutron fiuence, E I <1>, in units TABLE A.42 - Ambient and personal dose equivalent per unit
ofpSv cm2 for monoenergetic neutrons incident in various neutron fiuence, H*(lO) I <1> and Hp.slarf10, a) 1<1>, in units ofpSv
geometries on an adult anthropomorphic computational model. cm 2 for monoenergetic neutrons incident in various geometries on
These reference values are presented graphically in Figs. 22 and the ICRU sphere and slab. See Figs. 21 and 31-33
A.35 (Annex 1)
H* Hp,slab Hp,slab H p,slab H p,81ab Hp,slab Hp,aJab
Energy (10)1 (10,0°)1 (10, 15°)1 (10,30°)1 (10,45°)1 (10,60°)1 (10,75°)1
Energy
(MeV) ~ ~ ~ ~ ~ ~ ~
(MeV) AP PA RLAT LLAT ROT ISO

1.0 X 10- 9 5.24 3.52 1.36 1.68 2.99 2.40 1.00 X 10- 9 6.60 8.19 7.64 6.57 4.23 2.61 1.13
1.0 X 10- 8 6.55 4.39 1.70 2.04 3.72 2.89 1.00 X 10- 8 9.00 9.97 9.35 7.90 5.38 3.37 1.50
2.5 X 10- 8 7.60 1.99 2.31 4.40 3.30 2.53 X 10- 8 10.6 11.4 10.6 9.11 6.61 4.04 1.73
5.16
1.0 X 10- 7 9.95 2.58 2.86 5.75 4.13 1.00 X 10- 7 12.9 12.6 11.7 10.3 7.84 4.70 1.94
6.77
2.0 X 10- 7 11.2 2.92 3.21 6.43 4.59 2.00 X 10- 7 13.5 13.5 12.6 11.1 8.73 5.21 2.12
7.63
5.0 X 10- 7 12.8 3.35 3.72 7.27 5.20 5.00 X 10- 7 13.6 14.2 13.5 11.8 9.40 5.65 2.31
8.76
1.00 X 10- 6 13.3 14.4 13.9 12.0 9.56 5.82 2.40
1.0 X 10- 6 13.8 9.55 3.67 4.12 7.84 5.63
2.0 X 10- 6 14.5 10.2 3.89 4.39 8.31 5.96 2.00 X 10- 6 12.9 14.3 14.0 11.9 9.49 5.85 2.46
5.0 X 10- 6 15.0 10.7 4.08 4.66 8.72 6.28 5.00 X 10- 6 12.0 13.8 13.9 11.5 9.11 5.71 2.48
1.0 X 10- 5 15.1 4.16 4.80 8.90 6.44 1.00 X 10- 5 11.3 13.2 13.4 11.0 8.65 5.47 2.44
11.0
2.0 X 10- 5 15.1 4.20 4.89 8.92 6.51 2.00 X 10- 5 10.6 12.4 12.6 10.4 8.10 5.14 2.35
ILl

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


5.0 X 10- 5 14.8 ILl 4.19 4.95 8.82 6.51 5.00 X 10- 5 9.90 11.2 11.2 9.42 7.32 4.57 2.16
1.0 X 10- 4 14.6 4.15 4.95 8.69 6.45 1.00 X 10- 4 9.40 10.3 9.85 8.64 6.74 4.10 1.99
11.0
2.0 X 10- 4 14.4 10.9 4.10 4.92 8.56 6.32 2.00 X 10-4 8.90 9.84 9.41 8.22 6.21 3.91 1.83
5.0 X 10- 4 14.2 4.03 4.86 8.40 6.14 5.00 X 10- 4 8.30 9.34 8.66 7.66 5.67 3.58 1.68
10.7
1.00 X 10- 3 7.90 8.78 8.20 7.29 5.43 3.46 1.66
1.0 X 10- 3 14.2 10.7 4.00 4.84 8.34 6.04
2.00 X 10- 3 7.70 8.72 8.22 7.27 5.43 3.46 1.67
2.0 X 10- 3 14.4 10.8 4.00 4.87 8 .39 6 .05
5.0 X 10- 3 15.7 4.29 5.25 9.06 6.52 5.00 X 10- 3 8.00 9.36 8.79 7.46 5.71 3.59 1.69
11.6
1.0 X 10- 2 18.3 5.02 6.14 10.6 7.70 1.00 X 10- 2 10.5 11.2 10.8 9.18 7.09 4.32 1.77
13.5
2.0 X 10- 2 23.8 6.48 7.95 13.8 10.2 2.00 X 10- 2 16.6 17.1 17.0 14.6 11.6 6.64 2.11
17.3
3.0 X 10- 2 29.0 7.93 9.74 16.9 12.7 3.00 X 10- 2 23.7 24.9 24.1 21.3 16.7 9.81 2.85
21.0
5.0 X 10- 2 38.5 27.6 10.6 13.1 22.7 17.3 5.00 X 10- 2 41.1 39.0 36.0 34.4 27.5 16.7 4.78
7.0 X 10 2 47.2 13.1 16.1 27.8 21.5 7.00 X 10- 2 60.0 59.0 55.8 52.6 42.9 27.3 8.10
33.5
1.0 X 10- 1 59.8 16.4 20.1 34.8 27.2 1.00 X 10- 1 88.0 90.6 87.8 81.3 67.1 44.6 13.7
41.3
1.50 X 10- 1 132 139 137 126 106 73.3 24.2
1.5 X 10- 1 80.2 52.2 21.2 25.5 45.4 35.2
2.0 X 10- 1 99.0 25.6 30.3 54.8 42.4 2.00 X 10- 1 170 180 179 166 141 100 35.5
61.5
3.0 X 10- 1 133 38.6 71.6 54.7 3.00 X 10- 1 233 246 244 232 201 149 58.5
77.1 33.4
5.0 X 10- 1 188 46.8 53.2 99.4 75.0 5.00 X 10- 1 322 335 330 326 291 226 102
103
7.00 X 10- 1 375 386 379 382 348 279 139
7.0 X 10- 1 231 124 58.3 66.6 123 92.8
9.0 X 10- 1 267 79.6 144 108 9.00 X 10- 1 400 414 407 415 383 317 171
144 69.1
1.0 X 10° 282 154 74.5 86.0 154 116 1.00 X 10° 416 422 416 426 395 332 180
1.2 X 10° 310 175 85.8 99.8 173 130 1.20 X 10° 425 433 427 440 412 355 210
2.0 X 10° 383 247 129 153 234 178 2.00 X 10° 420 442 438 457 439 402 274
3.0 X 10° 432 308 171 195 283 220 3.00 X 10° 412 431 429 449 440 412 306
4.0 X 10° 458 345 198 224 315 250 4.00 X 10° 408 422 421 440 435 409 320
5.0 X 10° 474 366 217 244 335 272 5.00 X 10° 405 420 418 437 435 409 331
6.0 X 10° 483 380 232 261 348 282 6.00 X 10° 400 423 422 440 439 414 345
7.0 X 10° 490 391 244 274 358 290 7.00 X 10° 405 432 432 449 448 425 361
8.0 X 10° 494 399 253 285 366 297 8.00 X 10° 409 445 445 462 460 440 379
9.0 X 10° 497 406 261 294 373 303 9.00 X 10° 420 461 462 478 476 458 399
1.0 X 101 499 412 268 302 378 309 1.00 X 101 440 480 481 497 493 480 421
1.2 X 10 1 499 422 278 315 385 322 1.20 X 101 480 517 519 536 529 523 464
1.4 X 10 1 496 429 286 324 390 333 1.40 X 101 520 550 552 570 561 562 503
1.5 X 10 1 494 431 290 328 391 338 1.50 X 10 1 540 564 565 584 575 579 520
1.6 X 10 1 491 433 293 331 393 342 1.60 X 10 1 555 576 577 597 588 593 535
1.8 X 10 1 486 435 299 335 394 345 1.80 X 10 1 570 595 593 617 609 615 561
2.0 X 10 1 480 436 338 395 343 2.00 X 101 600 600 595 619 615 619 570
305
3.0 X 10 1 458 437 324 naa 395 na8 3.00 X 10 1 515 na8 na na na na na8
5.0 X 10 1 437 444 358 na 404 na 5.00 X 101 400 na na na na na na
7.5 X 10 1 429 459 397 na 422 na 7.50 X 101 330 na na na na na na
1.0 X 102 429 477 433 na 443 na 1.00 X 102 285 na na na na na na
1.3 X 102 432 495 467 na 465 na 1.25 X 102 260 na na na na na na
1.5 X 102 438 514 501 na 489 na 1.50 X 102 245 na na na na na na
1.8 X 102 445 535 542 na 517 na 1. 75 X 102 250 na na na na na na
2.01 X 102 260 na na na na na na
a Not available.
a Not available.

119
1'1
...,
.S
oj
Electron Data
;.a TABLEA.43-0rgan absorbed dose per unit fluence, DT/ <1>, in TABLE A.44 - Reference conversion coefficients from fluence to
oj
~ units of pGy cm2 and effective dose per unit fluence, E / <1>, in units directional dose equivalent for monoenergetic electrons and
til ofpSv cm2 for monoenergetic electrons incident in the AP normal incidence
e geometry on an adult anthropomorphic computational model
~ Energy H'(0.07,O')/<1>
(nSvcm 2 )
H'(3,O')/<1>
(nSvcm 2 )
H'(10, 0')/<1>
(nSvcm 2 )
r:il
...,rn Energy (MeV)
(MeV) 0.1 0.4 0.6 1.0 1.5 2.0 4.0 10.0
.§ 0.07 0.221
Organ 0.08 1.056
~ Skin 8 98 171 164 158 153 150 165 0.09 1.527
1'1
0
:p Testes 0 1 14 37 214 345 0.10 1.661
u
.s
0
Bone marrow
Stomach
0 1 5 11 28 52
0 3 184
0.1125
0.125
1.627
1.513
&:: Breast 0 14 43 75 200 325 0.15 1.229
tilu Liver 0 97 0.20 0.834
'6h Thyroid 0 121 297 0.30 0.542
0

~ Effective dose 0.1 1 1.5 2.7 5.9 11 44 131 0.40 0.455


oj 0.50 0.403

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


~ 0.60 0.366
.S 0.70 0.344 0.000
<Il
rn 0.80 0.329 0.045
::I
1.00 0.312 0.301
oS'"' 1.25 0.296 0.486
rn
~ 1.50 0.287 0.524
'0 1.75 0.282 0.512 0.000
IS<Il 2.00 0.279 0.481 0.005
0 0.417 0.156
Co) 2.50 0.278
1'1 3.00 0.276 0.373 0.336
.S
rn 3.50 0.274 0.351 0.421
'"'
<Il
>
4.00 0.272 0.334 0.447
1'1
0
5.00 0.271 0.317 0.430
Co) 6.00 0.271 0.309 0.389
7.00 0.271 0.306 0.360
8.00 0.271 0.305 0.341
10.00 0.275 0.303 0.330

TABLEA.45-Reference values of the angular-dependence factor, R(d, a.), at a depth, d, of 0.07 mm as a function of electron energy and
angle of incidence, a.

Energy R(0.07,cx)
(MeV) 0' IS' 30' 45' 60' 67.5' 75' 82.5' 85' 89'

0.07 1.000 0.813 0.461 0.170 0.041 naa 0.005


0.08 1.000 0.903 0.645 0.348 0.132 na 0.028 0.007 0.003
00 0.09 1.000 0.926 0.709 0.445 0.201 na 0.055 0.017 0.010 0.001
Ol 0.10 1.000 0.938 0.760 0.509 0.258 na 0.081 0.027 0.016 0.002
Ol
M
0.15 1.000 0.989 0.945 0.771 0.486 na 0.180 0.064 na na
r:--
LO 0.20 1.000 1.046 1.120 1.072 0.751 na 0.295 0.106 0.060 0.008
t0 0.40 1.000 1.039 1.143 1.330 1.348 1.082 0.661 0.245 0.133 0.015
Po 0.70 1.000 1.028 1.110 1.266 1.517 1.502 1.085 0.426 0.216 0.023
~ 1.00 1.000 1.017 1.087 1.227 1.469 1.583 1.308 0.552 0.294 0.030
~ 1.50 1.000 1.027 1.075 1.191 1.401 1.574 1.572 0.756 na na
~
Co)
..... 2.00 1.000 1.022 1.066 1.163 1.338 1.510 1.654 0.950 0.530 0.053
3.00 1.000 1.004 1.038 1.113 1.264 1.390 1.612 1.277 0.731 0.072
4.00 1.000 1.007 1.042 1.097 1.239 1.369 1.546 1.479 0.952 0.093
7.00 1.000 1.005 1.019 1.071 1.180 1.274 1.419 1.736 1.412 0.151
10.00 1.000 1.010 1.016 1.050 1.126 1.220 1.345 1.661 1.646 0.210
120 a Not available.
TABLE A.46- Reference values of the angular-dependence factor, R(d, a), at a depth, d, of 3 mm as a function of electron energy and angle
of incidence, ex

Energy R(3.a)
(MeV) 0° 15' 30° 45° 60' 67.5° 75° 82.5° 85° 89°

0.08 1.000 0.839 0.465 0.167 0.037 na" 0.003


1.00 1.000 0.905 0.657 0.346 0.127 0.063 0.027 0.007 0.004
1.50 1.000 0.951 0.798 0.548 0.276 0.172 0.086 0.029 0.015 0.002
2.00 1.000 1.000 0.940 0.746 0.425 0.267 0.138 0.047 0.026 0.003
4.00 1.000 1.036 1.134 1.272 1.039 0.741 0.412 0.142 0.078 0.007
7.00 1.000 1.009 1.052 1.177 1.399 1.215 0.762 0.274 na na
10.00 1.000 1.005 1.025 1.092 1.347 1.419 1.048 0.402 0.215 0.019
• Not available.

TABLEA.47 -Reference values of the angular-dependence factor, R(d, a), at a depth, d, of 10 mm as a function of electron energy and angle
of incidence, ex

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


Energy R(lO.a)
(M eV) 0° 15° 30° 45° 60° 67.5° 75' 82.5° 85° 89'

2.00 1.000 0.720 0.308 0.088 0.029 na" 0.010


3.00 1.000 0.898 0.636 0.334 0.115 0.056 0.022 0.005 0.003
5.00 1.000 1.011 1.939 0.718 0.363 0.212 0.101 0.031 0.016 na
7.00 1.000 1.023 1.113 1.041 0.664 0.407 0.202 0.064 0.034 na
10.00 1.000 1.017 1.083 1.211 1.008 0.694 0.360 0.114 0.060 na
" Not available.

121
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port PTB-ND. Physikalisch-Technische Bunde- DIETZE, G., HAIGHT, R C., KAWASHIMA, K., MENZEL,
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128
ICRU Reports
ICRU Reports are distributed by the ICRU Publications' office. Information on prices and how to order
may be obtained from:

ICRU Publications
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Copies ofthe reports may also be purchased from the following:

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Mrs. Brigitte Harder Dr. Minoru Takada
Konrad-Adenauer-StraBe 26 Japan Radioisotope Association
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Germany Bunkyoku Tokyo 113, Japan
Phone (0551) 22612
Dr. Torgil MOller
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The Japanese Society of Radiological Technology Lasarettet
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Unite de Radiobiologie et Radioprotection
UCL-Cliniques St. Luc
Avenue Hippocrate, 54.69
B-1200 Brussels, Belgium
Phone (02) 764.54.68

The currently available ICRU Reports are listed below.

ICRU
Report No. Title
lOb Physical Aspects of Irradiation (1964)
10c Radioactivity (1963)
10f Methods of Evaluating Radiological Equipment and Ma-
terials (1963)
12 Certification of Standardized Radioactive Sources (1968)
13 Neutron Fluence, Neutron Spectra and Kerma (1969)
15 Cameras for Image Intensifier Fluorography (1969)
16 Linear Energy Transfer (1970)
17 Radiation Dosimetry: X Rays Generated at Potentials of 5
to 150kV(1970)
18 Specification of High Activity Gamma-Ray Sources (1970)
20 Radiation Protection Instrumentation and Its Application
(1970)
22 Measurement of Low-Level Radioactivity (1972)
129
.S
~
23 Measurement ofAbsorbed Dose in a Phantom Irradiated
+'
o.:s by a Single Beam ofX or Gamma Rays (1973)
;.a
o.:s 24 Determination ofAbsorbed Dose in a Patient Irradiated
~
t; by Beams ofX or Gamma Rays in Radiotherapy Proce-
...~
<l)
dures (1976)
+'
~ 25 Conceptual Basis for the Determination of Dose Equiva-
lent (1976)
"'rn"
+'
~ 26 Neutron Dosimetry for Biology and Medicine (1977)
'ca
~ 27 An International Neutron Dosimetry Intercomparison
.S
~ (1978)
+'
u
<l)
28 Basic Aspects of High Energy Particle Interactions and
+'
...
0 Radiation Dosimetry (1978)
~ 30 Quantitative Concepts and Dosimetry in Radiobiology
t;
u
'So
(1979)
'0
0 31 Average Energy Required to Produce an Ion Pair (1979)
;.a 32 Methods ofAssessment ofAbsorbed Dose in Clinical Use
o.:s
~ of Radionuclides (1979)

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


.S 33 Radiation Quantities and Units (1980)
<l)
rn
;:j 34 The Dosimetry of Pulsed Radiation (1982)
... 36 Microdosimetry (1983)
<8
rn
+'
~
37 Stopping Powers for Electrons and Positrons (1984)
.~
u
38 Dose and Volume Specification for Reporting Intracavi-
!:S
<l)
tary Therapy in Gynecology (1985)
0
u 39 Determination of Dose Equivalents Resulting from Exter-
~
0 nal Radiation Sources (1985)
'00
...
<l)
40 The Quality Factor in Radiation Protection (1986)
:> 41 Modulation Transfer Function of Screen-Film Systems (1986)
~
0
u 42 Use of Computers in External Beam Radiotherapy Proce-
dures with High-Energy Photons and Electrons (1987)
43 Determination of Dose Equivalents from External Radia-
tion Sources-Part 2 (1988)
44 Tissue Substitutes in Radiation Dosimetry and Measure-
ment (1989)
45 Clinical Neutron Dosimetry - Part I: Determination of
Absorbed Dose in a Patient Treated by External Beams
of Fast Neutrons (1989)
46 Photon, Electron, Proton and Neutron Interaction Data
for Body Tissues (1992)
46D Photon, Electron, Proton and Neutron Interaction Data
for Body Tissues, with Data Disk (1992)
47 Measurement of Dose Equivalents from External Photon
and Electron Radiations (1992)
48 Phantoms and Computational Models in Therapy, Diag-
nosis and Protection (1992)
49 Stopping Powers and Ranges for Protons and Alpha
Particles (1993)
00
49D Stopping Powers and Ranges for Protons and Alpha
0>
0>
Particles, with Data Disk (1993)
,.....
rc.: 50 Prescribing, Recording and Reporting Photon Beam
to Therapy (1993)
...0
+'
51 Quantities and Units in Radiation Protection Dosimetry
0..
~
<l)
(1993)
~ 52 Particle Counting in Radioactivity Measurement (1994)
~
u
...... 53 Gamma-Ray Spectrometry in the Environment (1994)
54 Medical Imaging - The Assessment ofImage Quality (1995)
55 Secondary Electron Spectra from Charged Particle Inter-
actions (1995)
130
56 Dosimetry of External Beta Rays for Radiation Protection
57 Conversion Coefficients for Use in Radiological Protection
against External Radiation

Binders for ICRU Reports are available. Each binder will accommodate from six to eight reports. The binders
carry the identification, "ICRU Reports", and come with label holders which permit the user to attach labels
showing the Reports contained in each binder.
The following bound sets ofICRU Reports are also available:
Volume I. ICRU Reports lOb, 10c, 10f
Volume II. ICRU Reports 12, 13, 14, 15, 16, 17, 18,20
Volume III. ICRU Reports 22, 23, 24, 25, 26
Volume IV. ICRU Reports 27, 28, 30, 31, 32
Volume V. ICRU Reports 33, 34, 35, 36
Volume VI. ICRU Reports 37,38,39,40,41

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Volume VII. ICRU Reports 42, 43, 44
Volume VIII. ICRU Reports 45, 46, 47
Volume IX. ICRU Reports 48, 49, 50, 51
(Titles of the individual Reports contained in each volume are given in the list of Reports set out above.)
The following ICRU Reports are now superseded and/or out of print:

ICRU
Report No. Title and Reference *
1 Discussion on International Units and Standards for
X-ray work, Br. J. Radiol. 23, 64 (1927).
2 International X-Ray Unit of Intensity, Br. J. Radiol. (new
series) 1,363 (1928).
3 Report of Committee on Standardization ofX-ray Mea-
surements, Radiology 22,289 (1934).
4 Recommendations of the International Committee for Ra-
diological Units, Radiology 23,580 (1934).
5 Recommendations of the International Committee for Ra-
diological Units, Radiology 29,634 (1937).
6 Recommendations of the International Commission on
Radiological Protection and of the International Com-
mission on Radiological Units, National Bureau of
Standards Handbook 47 (U.S. Government Printing
Office, Washington, D.C., 1951).
7 Recommendations of the International Commission on
Radiological Units, Radiology 62, 106 (1954).
8 Report of the International Commission on Radiological
Units and Measurements (lCRU) 1956, National Bu-
reau of Standards Handbook 62 (U.S. Government
Printing Office, Washington, D.C., 1957).
9 Report of the International Commission on Radiological
Units and Measurements (lCRU) 1959, National Bu-
reau of Standards Handbook 78 (U.S. Government
Printing Office, Washington, D.C., 1961).
lOa Radiation Quantities and Units, National Bureau of
Standards Handbook 84 (U.S. Government Printing
Office, Washington, D.C., 1962).
10d Clinical Dosimetry, National Bureau of Standards Hand-
book 87 (U.S. Government Printing Office, Washington,
D.C., 1968).
131
10e Radiobiological Dosimetry, National Bureau of Standards
Handbook 88 (U.S. Government Printing Office, Wash-
ington, D.C., 1963).
11 Radiation Quantities and Units (International Commis-
sion on Radiation Units and Measurements, Washing-
ton, D.C., 1968).
14 Radiation Dosimetry: X Rays and Gamma Rays with
Maximum Photon Energies Between 0.6 and 50 MeV
(1969).
19 Radiation Quantities and Units (International Commis-
sion on Radiation Units and Measurements, Washing-
ton, D.C., 1971).
19S Dose Equivalent [Supplement to ICRU Report 19] (Inter-
national Commission on Radiation Units and Measure-
ments, Washington, D.C., 1973).
21 Radiation Dosimetry: Electrons with Initial Energies Be-
tween 1 and 50 Me V (International Commission on Ra-
.S

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diation Units and Measurements, Washington, D.C.,
1972).
29 Dose Specification for Reporting External Beam Therapy
with Photons and Electrons (International Commission
on Radiation Units and Measurements, Washington,
D.C., 1978)
35 Radiation Dosimetry: Electron Beams with Energies Be-
tween 1 and 50 Me V (1984).

*References given are in English. Some of the Reports were also published in other languages.

132
Index
Absorbed dose, ix, 6 Photons, 83,106
Absorbed dose distributions, 6, 13, 16 Comparison of data, 52
Absorbed dose in the gonads as a function of energy, 41 Electrons, 52
Absorbed dose to various organs Comparisons between quantities, 61
Electrons, 120 Electrons, 60
Neutrons, 90-104, 111-118 Neutrons, 59, 63
Photons, 81-90, 105-109 Photons, 57, 58, 62
Age- and sex-specific models, 15 Comparison of conversion coefficients for effective dose and the
Age dependence of effective dose effective dose equivalent
Electrons, 50 Photons, 58, 67
Photons, 30 Comparison of effective dose, ambient dose equivalent and per-
Aligned field, 10 sonal equivalent, 64
Ambient dose equivalent, ix, 11 Neutrons, 64
Electrons, 50 Comparison of effective dose and a mbient dose equivalent

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Neutrons, 49, 63, 119 Neutrons, 68
Performance, 65 Photons, 67
Personal dose equivalent, 119 Comparison of effective dose and effective dose equivalent
Photons, 31 , 67 Electrons, 62
Angle ex for H ' (d, ex) and Hp(d, ex ), 11 Neutrons, 60
Angular dependence Comparison of dose equivalent determinations in the ICRU
Electrons, 52, 54, 55 sphere and ICRU slab, 50
Angular dependence factors, 63 Electrons, 50
Electrons, 120, 121 Comparison of effective dose and other quantities, 68
Angular dependence of the conversion coefficient, 50 Photons, 69, 70,71,72, 73
Neutrons, 50 Comparison of protection and operational quantities, 65
Angular dependence of effective dose, 29, 41, 50 Irradiation geometries, 65
Electrons, 50 Computer codes
Photons, 29, 30 Electrons, 47
Angular variation, 45 Neutrons, 35
Neutrons, 45 Photons, 23
Angular variation of effective dose for photons, 29, 30 Transport codes, 23
Annexes, 78 Contents, iii
Contents, 78 Continuous slowing-down approximation, 17
Anthropomorphic models, 15 Contributions of specific organs and tissue to effective dose, 34,
Approximation of Hp for neutrons, 74 44,50
Equivalent doses to small organs, 74 Electrons, 50
Approximations to H p for photons, 72 Neutrons, 42
Area monitoring, 66 Photons, 30, 32, 33
Photons, 66 Contributions of specific organs to effective dose and to the effec-
Neutrons, 66 tive dose equivalent
Neutrons, 61
Baby model, 16 Photons, 59
Bladder absorbed dose Contributions of specific organs to effective dose as a function of
Neutrons, 90, 111 energy for neutrons , 43, 45, 46, 47, 48
Photons, 105 Conversion coefficients, 2, 3, 4, 22, 23
Bone, 17 Age dependence, 30, 42
Bone (red marrow) absorbed dose Ambient dose equivalent, 31, 43
Neutrons, 91, 112 Angular dependence, 41 , 45
Photons, 105 Calculations, 51
Bone (surface) absorbed dose Directional dose equivalent, 33, 44
Neutrons, 91, 112 Effective dose, 27, 28, 31, 38, 40
Photons, 82, 105 Electrons, 47, 48, 49, 52,120
Breast (female) absorbed dose, 82 Energy dependence, 28, 40, 41
Neutrons, 113 Methods of calculation, 23, 35, 47
Photons, 82, 106 Models, 25, 36, 48
Broad spectra, 14, 22 Neutrons, 34,37, 40, 41 , 42, 43, 45, 49, 63
Operational quantities, 26, 30, 37, 39, 42
Calculating absorbed dose distributions, 16 Personal dose equivalent, 33, 44
Calibration quantities, 3 Phantoms, 25, 36, 48
Changes in the protection quantities, 61 Photons,23,27,31,33, 58,105,llO-lll
Charged particle equilibrium, 14 Physical data, 25, 36, 49
Child models, 15, 16 Protection quantities, 25, 27, 36, 39, 49
Colon absorbed dose Reference conversion coefficients, 22
Neutrons, 92, 113 Remainder, 40 133
Selected organs, 37 Organ absorbed dose, 120
Statical uncertainties, 26, 37 Organ and tissue doses, 49
Variability of the data, 26, 37 Personal dose equivalent, 64, 75, 76
Conversion coefficients for the ambient dose equivalent, 110 Protection quantities, 49, 60
Photons, 110 Ratio of the skin dose Hp,sltin, t the directional dose equivalent,
Conversion coefficients for ambient dose equivalent and effective H'(0.07;OO), 77
dose in various irradiation geometries as a function of pho- Reference conversion coefficients, 54, 56, 120
ton energy, 67 Reference values ofthe angular-dependence factor, 56, 120,
Conversion coefficient for directional dose equivalent, 110 121
Photons, 110 Skin dose, 75
Conversion coefficients for operational quantities and effective Special considerations, 46
dose as a function of photon energy, 69, 73 Uncertainties, 52
Conversion coefficients for H p,slab(10, <X ) as a function of energy Variability of the data, 52, 53, 54
and angle of incidence for neutrons, 49 Energy dependence, 54
Conversion coefficients for operational quantities and effective Electrons, 54
dose as a function of photon energy, 71, 72 Energy dependence of effective dose, 28, 40
Electrons, 50
Data Energies for conversion coefficients, 22
Electrons, 49 Energy imparted, ix
Neutrons, 36 Equivalent dose, x
Photons, 25 Equivalent dose , 9, 57

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Data for effective dose from neutrons in various geometries, 102- Equivalent doses to small organs, 72
104 Evolution of quantities, 3
Data for mean absorbed dose to various organs, 96 Expanded and aligned fields, 10
Neutrons, 96-102 Eye lens absorbed dose
DEEP transport code, 18 Photons, 89, 109
Determination of absorbed dose distributions, 13
Directional dose equivalent, ix, 11 Female models, 15
Electrons, 50, 63, 75 Field quantities, 13, 14
Neutrons, 44, 63 Fluence, x
Photons, 62 Foreword, v
Distribution of the absorbed dose, 13
Dose equivalent, ix, 3, 10, 57 Geometries used with the ICRU sphere, 21
Dose equivalent index, ix, 4 Geometries used with the ICRU slab, 21
Dose in bone, 17 Glossary of terms and definitions of quantities, ix
Gonads, female (ovaries) absorbed dose
Effective dose, ix, 9, 10, 28, 29, 38, 57 Neutrons, 92, 114
Age dependence, 30, 42 Photons, 83
Angular dependence, 29, 41 Gonads, male (testes) absorbed dose
Conversion coefficients, 29, 40 Neutrons, 92, 114
Electrons, 75, 120 Photons, 84, 106
Neutrons, 40, 50, 74 Gonads absorbed dose (mean of ovaries and testes), 93
Photons, 26, 27, 67, 68 Neutrons, 92, 114
Specific tissue and organs, 30, 42 Photons, 84, 106
Effective dose as a function of energy and age, 42 Gonads absorbed dose (mean of ovaries and testes), 93
Effective dose equivalent, ix, 5, 57 Neutrons, 93, 115
Effective dose from neutrons in various geometries, 102-104 Photons, 84
Effective dose per unit air kerma, 31 Gonads absorbed dose, 107
Photons, 88, 109 Photons, 107
Effective dose per unit neutron fiuence GSF - national research center for environment and health
Neutrons, 95, 119 codes, 19
EGS4,18
Electrons, 46-56 HADRON code, 19
Absorbed dose to various organs, 120 History of quantities, 3
Age dependence of the effective dose, 50 HL-PH code, 19
Angular dependence, 52, 54 Human body models and phantoms, 15
Angular-dependence factor, 120, 121
Angular dependence of effective dose, 50 ICRP Publication 51,5
Comparison of effective dose and effective dose equivalent, 62 ICRP Publication 60, 5
Contribution of specific organs and tissues to the effective dose, ICRU Report 51, 6
50 ICRU Report 40, 5
Conversion coefficients, 46, 47, 48, 49, 52,120 ICRU Report 47, 6
Data, 49,120--121 ICRU slab, 16, 21 , 50
Directional dose equivalent, 62, 63,75 ICRU sphere, 16, 21, 50
Effective dose, 50, 75, 76 ICRU sphere, 50
Energy dependence, 54 ICRU sphere model, 16
Energy dependence of effective dose, 50 Individual monitoring
Methods for calculating conversion coefficients, 47 Neutrons, 74
Models and phantoms, 48 Photons, 68
134 Operational quantities, 52 Individual dose equivalent, x
Infant models, 15 Energy dependence of effective dose, 40, 42
Introduction, 1 Evaluated and original data for effective dose from neutrons in
Irradiation geometries, 20, 41 various geometries, 102-104
Photons, 26 Evaluated and original data for mean absorbed dose to various
Isotropic geometry, 20 organs, 96--102
Individual monitoring, 74
Kerma,x Methods for calculating conversion coefficients, 35
Kerma approximation, 14, 17 Organ absorbed dose, 37
Organ dose, 37
LAHET code, 19 Operational quantities, 37
Lateral geometry, 20 Performance of ambient dose equivalent, 65
Linear energy transfer, x, 8 Personal dose equivalent, 44, 63, 74, 119
Liver absorbed dose Protection quantities, 39, 59
Neutrons, 93, 115 Ratio of EIH* (10) and E IHp,slab (10), 68
Photons, 85, 107 Ratio EIHp,testes for several irradiation geometries, 76
Lung absorbed dose Ratio EIHp,tbymus for several irradiation geometries, 76
Neutrons, 85, 107 Reference conversion coefficients, 40, 41, 49
Photons, 85, 107 Special considerations, 34
Specific organs and tissues, 44, 45, 46, 47, 48, 61

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MADE,4 Skin dose and directional dose equivalent, 75
MCNP code, 19 Transport codes, 35
MCNPE-BO Code, 19 Tissue dose, 37
MCNP4 code, 19 Uncertainties, 37
MORSE-CG code, 19 Variability of the data, 37, 39
Male models, 15 Variability of organ absorbed dose conversion coefficients, 38
Mathematical model phantom, 15
Maximum dose equivalent, 4 Oesophagus absorbed dose
Mean quality factor, xi Neutrons, 94, 116
Mean absorbed dose, 6, 9 Photons, 86, 107
Mean absorbed dose to various organs, 96 Organ absorbed dose, 9
Neutrons, 96--102 Electrons, 120
Mean quality factor, 7, 8, 9 Neutrons, 37
Methods for calculating conversion coefficients Organ and tissue doses
Electrons, 47, 51 Electrons, 49
Neutrons, 24, 35 Neutrons, 39
Photons, 23 Organ dose, x
MIRD phantom, 15 Neutrons, 37
Mixed radiation fields, 14, 22 Photons, 27
Models and phantoms, 25 Organ equivalent doses, 27
Electrons, 48 Organs, xi, 32, 33
Human body, 15 Neutrons, 43, 44, 46,47, 48,61
Neutrons, 36 Photons, 30, 34, 59
Model conformity with ICRP specifications, 16 Operational quantities, x, 1,3,5, 10, 22, 26, 30, 39, 62
Monitoring, 11 Electrons, 52
Monte Carlo technique, 17 Neutrons, 37, 42
Summary, 76
Neutron conversion coefficients, 24, 25
Neutrons Pediatric model, 16
Absorbed dose in gonads, as a function of energy, 41 Paris statement ofthe ICRP, 5
Absorbed dose to various organs, 111-118 Performance of ambient dose equivalent, 65
Age dependence of effective dose, 42 Neutrons, 65
Ambient dose equivalent, 42, 63, 119 Performance of operational quantities, 64
Analysis, 39 Personal dose equivalent, xi, 11, 33, 44, 119
Angular dependence, 45 Electrons, 56, 64, 75, 76
Angular dependence of conversion coefficient, 50 Neutrons, 63,74, 119
Angular dependence of effective dose, 41 Photons, 63, 78, 72
Area monitoring, 66 Phantoms of the human body, 15
Calculations, 24 Photon conversion coefficients, 22, 23
Comparison of effective dose, ambient dose equivalent and per- Photons, 22-33
sonal dose equivalent, 64 Absorbed dose to various organs, 105-109
Comparison of effective dose and effective dose equivalent, 60 Absorbed dose to various organs per unit air kerma, 81-90
Comparison of effective dose and other quantities, 68 Age dependence of effective dose, 30
Computer codes, 35 Ambient dose equivalent, 31, 62, 110
Contribution of specific organs and tissues to effective dose, 42 Angular dependence of effective dose , 29
Conversion Coefficients, 35, 37, 38, 39, 40, 44, 49, 50, 63 Area monitoring, 66
Data, 36, 112-118 Calculations, 23
Directional dose equivalent, 44, 63 Comparison of effective dose and ambient dose equivalent, 67
Effective dose, 38, 41,74 Comparison of effective dose and other quantities, 69, 72, 73
Effective dose as a function of energy and age, 42 Contributions of specific organs to effective dose, 32
Effective dose per unit neutron fiuence, 95, 119 Conversion coefficients, 27, 58, 67,105,110,111 135
Conversion coefficients for the ambient dose equivalent, 110 Ratios EIHp,Blob (10) and EIH'(10) for several irradiation geom-
Conversion coefficient for directional dose equivalent, 110 etries
Conversion coefficients for operational quantities and effective Photons, 74
dose as a function of photon energy, 69, 70, 71, 72, 73 Ratio EIHp,slab for several irradiation geometries
Data, 25, 105-109 Photons, 75
Directional dose equivalent, 33, 110 Ratio EIHp,testes for several irradiation geometries
Effective dose, 27, 68 Neutrons, 76
Effective dose per unit air kerma, 109 Ratio EIHp,testes for several irradiation geometries
Energy dependence of effective dose, 28 Neutrons, 76
Individual monitoring, 68 Ratio E IH*(1 0)
Operational quantities, 26 Neutrons, 68
Personal dose equivalent, 33, 63, 72 Photons, 67
Protection quantities, 57 Ratio EIH*(10 ) and ElH p.s1ab(10)
Ratio of EIH*(10 ), 67 Neutrons, 68
Ratios E IH p,slob(10, 0°) and E IH'( 10, 0°) as a function of photon Ratios of effective dose, E, to H *( 10) and H p,Blab(lO, 0°)
energy, 69 Neutrons, 64
Ratios EIHp,slob(lO, 180°) and EIH' (10, 180°), 70 References, 122
Ratios E(LAT)H'(lO, 90°), 71 Reference angular dependence factors
Ratios EIHp,slob(ROT) and EIH'(10, ROT), 72 Electrons, 56
Ratio E(ISO)lH'(10, ISO), 73 Reference conversion coefficients
Ratios EIHp,slab(10) and EIH'(10) for several irradiation geom- Ambient dose equivalent, 31, 43, 49

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etries,74 Directional Dose equivalent, 33
Ratio E IHp,slob for several irradiation geometries, 75 Effective dose, 28, 31, 41
Reference conversion coefficients, 28 Electrons, 52, 56, 120
Special considerations, 23 Neutrons , 34, 40, 41 , 43, 49
Specific organs, 59 Personal dose equivalent, 33
Variability ofthe data, 26 Photons, 22, 27,28, 31
Uncertainties, 26 Reference depth, 11
Physical data, 25 Reference man, 15
Electrons, 49 Reference models, 16
Neutrons, 36 Reference values of the angular-dependence factor for electrons,
Physical quantities, 3, 22 55,120,121
Physical phantom, 15 Relationship between Hp(d), and E, 12
Postero-anterior geometry, 20 Relationships between quantities
Preface, vii Changes in the protection and operational quantities, 57
Procedure, 10 General Conclusions, 77
Protection and Operational quantities for electrons, 52 Relationships between the protection and operational quantities:
Protection quantities, xi, 1,3, 9, 22, 25, 27, 36 the performance of the operational quantities, 64
Electrons, 60 Relative biological effectiveness, xi
Neutrons, 59 Remainder, 9, 10,40, 59
Photons, 57 Remainder absorbed dose
Summary, 61 Neutrons, 94, 117
PTBIBG code, 19 Photons, 86, 108
Remainder dose evaluation, 10
Q, xi, 7, 8, 9 Rotational geometry, 20
Q(L)-relationship,7
Q(L)-L relationship, 8, 9, 63 SAM-CE code, 20
Quality factor, xi, 1, 7 Sex-specific adult models, 15
Quality factor as a function oflinear energy transfer, 8 Simple phantoms, 15
Quantities, ix Skin absorbed dose
Quantities used in radiological protection, 3 Electrons, 75
Neutrons, 94, 117
Radiation energy spectra and mixed radiation fields, 22 Photons, 87, 108
Radiation field , 13, 14 Skin dose and directional dose equivalent, 75
Radiation quality, 1 Neutrons, 75
Radiation transport, 17 Slab phantoms, 15, 16
Radiation weighting factor, x, xi, 1, 6, 7 Specific organs and tissue, 32, 33, 42
Ratio R(0.7, a)IR(0.7, a), 54 Neutrons, 44,46,47,48,61
Ratio EIHE for incident electrons, 62 Photons, 34, 59
Ratio EIHE for several irradiation geometries Special consideration for electrons, 46
Photons, 58 Special considerations for photons, 23
Ratios EIHp,Blab(10, 0°) and EIH'(10 , 0°) as a function of photon Spherical and slab phantoms, 15
energy, 69 Spherical tissue-equivalent model, 16
Ratios EIH p,slab(10, 180°) and EIH'( 10 , 180°),70 Standard and reference models and phantoms, 16
Ratios E(LAT)H'(10, 90°) Statistical uncertainties, 26
Photons, 71 Neutrons, 37
Ratios ElHp,Blab(ROT) and EIH '(10, ROT) Stomach absorbed dose
Photons, 72 Neutrons, 95, 118
RatioE(ISO)IH'(10, ISO) Photons, 87, 108
136 Photons, 73 Stopping power, 8, 9
Tables, 105 MCNP4 Code, 19
Thymus a bsorbed dose MORSE-CG Code, 19
Photons, 89, 109 Neutrons, 35
Thyroid absorbed dose PTBIBG Code, 19
Neutrons, 95, 118 SAM-CE code, 20
Photons, 88, 108
Tissue dose Uncertainties
Photons, 27 Electrons, 53, 54
Tissue weighting factors, ix, xi Neutrons, 37
Tissues,xi,30, 32,33 Photons, 26
Neutrons,43,44,46,47,48,61 Units, ix, xi
Photons, 30, 34, 59 Uterus absorbed dose
Tissue dose Photons, 90, 109
Neutrons, 37, 39
Transport codes, 17, 18 Variability of the data
Deep,18 Electrons, 52, 54
EGS4 code, 18 Photons, 26
EGS4 (*) code, 18 Variation of effective doses with age, 30
EGS4 (**) code, 18 Variability of effective dose conversion coefficients, 39

Downloaded from http://jicru.oxfordjournals.org/ at University of Sussex on July 10, 2016


ETRAN,18 Neutrons, 39
FANEUT, 18 Variation of effective dose with age
GSF-national research center for environment and health Electrons, 50
codes, 19 Neutrons, 42
HADRON. 19 Variability of operational quantity data for electrons, 53
HL-PH,19 Variability of organ absorbed dose conversion coefficients, 38
JEUNESSE, 19
LAHET code, 19 wR,7
MCNP code, 19 wT, xi
MCNPE-BO code, 19 Weighting factors , ix, xi, 7

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