An Introduction to Laterite

Products and processes of intensive rock weathering

W. Schellmann

Historical development

Laterite is well known in Asian countries as a building material for more than 1000 years. It was
excavated from the soil and cut in form of large blocks; temples at Angkor are famous examples
for this early use. At begin of the 19.century it obtained scientific interest when the English
surgeon Francis Buchanan travelled along the western coast of southern India and published his
manifold observations and results. He coined the term laterite when he wrote (1807): What I
have called indurated clay is one of the most valuable materials for building. It is diffused in
immense masses, without any appearance of stratification and is placed over the granite that
forms the basis of Malayala. It is full of cavities and pores, and contains a very large quantity of
iron in the form of yellow and red ochres. In the mass, while excluded from the air, it is so soft,
that any iron instrument readily cuts it, and is dug up in square masses with a pick-axe, and
immediately cut into the shape wanted with a trowel, or large knife. It very soon after becomes
as hard as brick, and resists the air and water much better than any brick that I have seen in India.
The most proper English name would be laterite, from lateritis, the appellation that may be
given to it in science. (The Latin word later means brick)

These statements were the start of a tremendous number of studies of this strange material,
hitherto resulting in more than 2000 publications. Above all geologists dealt at first with laterite
but in later epochs also soil scientists, mineralogists, geographers, geomorphologists, mining and
construction engineers participated in laterite research. The great interest of so many scientists
with their different viewpoints did not only result in a great increase in knowledge but created
also a great confusion in the basic understanding and interpretation of laterite formation. .

In the last fifty years many soil scientists devoted to laterite research and contributed their
specific experience with soil forming processes. A major role was seen in the movement and
precipitation of dissolved iron (absolute iron accumulation) in contrast to the predominant
interpretation by residual (relative) enrichment due to removal of silica and other soluble
elements. It was assumed that the iron

- migrated upwards from deeper layers (early theory of capillary rise).

- migrated downwards from the overlying soil and concentrated in deeper illuvial horizons.

- migrated laterally in the ground water and precipitated within the zone of a fluctuating ground
water table (ground water laterite). Other scientists stressed the origin of iron from higher
areas in the landscape (plateaus, low hills) and precipitation in deeper parts above all at the foot
of slopes. Geomorphologists even suggested that all laterites formed by such processes and their
frequent positions on top of plateaus were caused by a subsequent inversion of the relief.
Other difficulties resulted by the introduction of soil names such as oxisol, latosol and ferralitic
soil and their definition by specific soil properties. They are without doubt useful within the
systems of international soil classification but not practicable for geologists dealing with thick
laterite mantles and huge lateritic ore deposits as bauxites and nickel laterites. These occurrences
cannot be considered as soils which should be restricted to loose surface covers and not extended
to complete weathering mantles with thicknesses up to ten meters and locally more.

The different interpretations of laterite became occasionally rather exotic because of the
conflicting laterite aspects and designations. Even nowadays the differences are not wholly
overcome but in the last decades many studies contributed to a better and undivided
understanding. Thus the International Geological Cooperation Programme No. 129
Lateritisation Processes which was sponsored 1975-1983 by UNESCO and the Union of
Geological Sciences accelerated laterite research in all parts of the world. Eurolat was started
1984 by French geoscientists as European Network on Tropical Laterites. Moreover, an
International Interdisciplinary Laterite Reference Collection (CORLAT) was established at the
International Soil Reference and Information Centre (ISRIC) at Wageningen, the Netherlands.

Modern interpretation of laterite formation

Laterites are the products of intensive and long lasting tropical rock weathering which is
intensified by high rainfall and elevated temperatures. Formation of most of the laterites started
in the Tertiary. For a proper understanding of laterite formation we must focus on the chemical
reactions between the rocks exposed at the surface and the infiltrated rain water. These reactions
are above all controlled by the mineral composition of the rocks and their physical properties
(cleavage, porosity) which favour the access of water. The second relevant factor for the
formation of laterites are the properties of the reacting water (dissolved constituents,
temperature, acidity pH, redox potential Eh) which are themselves controlled by the climate,
vegetation and the morphology of the landscape.

Tropical and subtropical areas show generally a rather high annual precipitation but its temporal
distribution varies strongly from countries with pronounced and long lasting dry seasons to
equatorial areas with a more continuous precipitation. Chemical weathering slows down in dry
seasons at least above the fluctuating water table. Aqueous dissolution of minerals proceeds
when a chemical equilibrium is not arrived i.e. when the dissolved constituents are removed in
the water. The chemical reactions are further controlled by the activity of water which is equal to
one in freely moving water but lowered within small pores in the soil. Stability and reaction rate
vary from mineral to mineral; e.g. quartz is more stable than feldspar. Minerals of the same
species e.g. kaolinite can show different crystallinity which equally controls their stability.
Strongest alteration proceeds at the surface of the parent rock whereas it is lower in the regolith
above the rock.

The principal effects of the various factors on laterite formation are well known but it is difficult
to determine them in space and time in the field. In the practise of laterite research most valuable
informations are obtained by detailed studies of complete weathering sections (laterite profiles)
reaching from the unweathered parent rock to the strongly altered surface layer. Sections
showing physical disturbances as erosion or importation of transported material should be
omitted to exclude effects other than weathering. An adequate number of laterite profiles on
different parent rocks has been analysed which enable a clear understanding of the basic
processes of lateritization.

The chemical and mineralogical results have shown that the primary minerals are generally not
fully dissolved but partially transformed in secondary minerals which are more stable under the
intensive weathering conditions. The elements in the primary rock minerals are released and
show different reactions in the aqueous solution. The elements Na, K, Mg and Ca do not react
with other elements and are removed in the percolating water. The initial dissolution is
predominantly promoted by a higher acidity (lower pH) of the water. A high percentage of the
dissolved Si is equally removed but another part reacts with dissolved Al and forms the clay
mineral kaolinite. The aluminium hydroxide gibbsite is formed if the concentration of dissolved
Si is extremely low due to a very strong drainage. Dissolved Fe is very reactive with hydroxyl
ions and forms after oxidation goethite and hematite which cause the red-brown colour of
laterites. Thus the dominant process of laterite formation is the residual (or relative) enrichment
of iron and frequently of aluminium by removal of silica, alkalis and alkaline earths. This
chemical alteration corresponds mineralogically with the formation of goethite, hematite,
kaolinite and gibbsite. These minerals together with relicts of partially dissolved quartz form the
bulk of laterites.

The transformation of rock into laterite proceeds in general gradually as indicated by the steady
increase of iron and decrease of silica in laterite profiles above the parent rock. It goes without
saying that the initial products of weathering can not be called laterites. They also form in
moderate climates and are essentially kaolinized rocks still showing the structure of the rock.
They are called saprolites in which iron is not as strongly concentrated as in laterites. Some
saprolites show due to finely disseminated hematite a deep-red colour and are sometimes
erroneously considered as laterite. Saprolites as well as laterites are presently classified as
residual rocks which in their part can be seen as an individual rock group.

A modern laterite definition should comprise all products of intensive tropical weathering
independent of their properties and parent rocks, but exclude products of weaker weathering
which also occur in moderate climate. Redbrown laterites on granites, granitic gneisses, clays
and shales are generally hard or harden after drying, whereas laterites an basalts are commonly
friable and show an intensive reddish color. Lateritization of alkaline rocks (nepheline syenites,
phonolites) often results in formation of highly aluminious laterites (bauxites) with lighter color.
On ultramafic rocks (serpentinites etc.) forms very soft, yellow-brown Ni-bearing goethite
(nickel limonite ore). All these weathering products are formed by the same fundamental
weathering process and are therefore different members of a laterite family.

Properties and definition of laterites are controversially discussed since Buchanan (1807)
introduced this term in geosciences. Publications with the title "What is Laterite?" are evidence
of a widespread confusion .Even presently the controversy is not overcome, allthough intensive
research has greally increased the knowledge on laterite. A disputed definition is commonly,
however, not due to a lacking knowledge but to a missing agreement among the interested
scientists: moreover a good definiion is qute another matter as a comprehensive description.
Already Aristoteles (384-322 AC) required that a scientific definiton must specify the catagory
of the defined matter (here: residual rocks) and the difference to other subjects in the same
catagory (here: saprolites) . Following this instruction the author of this article suggested in
cooperation with the IGCP-Projects 129 "Laterisation Processes" a new laterite definion
(Schellmann 1986) on the basis of defining ratios Si : (Al+Fe) which differs with the
composition of the parent rock This proposal was critisized by Bourman and Ollier ((2002) as
too complicated without giving another clear proposal. A quite other suggestion was
contributed by Tardy (1997) who favors to designate each red soil as laterite. In consequence of
this proposal he calculated that about one third of the continental land mass is covered by
laterites.

Absolute iron accumulation which was frequently discussed in laterite papers is presently no
longer regarded as a fundamental process in the formation of extended laterite layers. Iron
accumulation after a lateral transport should cause iron depletion in neighbouring areas which is
generally not observed. Stronger downward leaching in the profile or even from the top of a
platau to slope position is posulated in several papers. This could happen in an acicic and
reducing environment , but low pH- and Eh- values are normally not realized under conditions
of strong precipitation and good drainage. Swampy environments do not correspond with the
requirements for laterite formation. On the other hand migration and precipitation of
dissolved iron is indicated by the presence of iron mottles, nodules and concretions in laterite
horizons. Therefore the author takes absolute iron accumulation definitely into account, but only
in shorter ranges and on a minor scale.

Lateritic weathering is only one relevant process wich is active in the superficial zone of tropical
regions. Erosion or denudation, respectively, contribute equally to an alteration at the surface
together with deposition of material by water and wind. Not each variation in lateritic profiles
can be attributed to chemical weathering. There are ironstone formations in the world which can
hardly be interpreted by normal lateritization processes. If they show signs of reworking,
transport and deposition they should not be defined as laterites but as lateritic sediments.
Lateritic sediments of older epochs can be overprinted by younger lateritic weathering. Complex
lateritic occurrences are grouped as exolaterites, false laterites and laterite derivative facies. They
are relevant in regional studies but not for a general understanding of the lateritization process.
This is equally true for loose surface layers above autochthonous laterites, locally separated by a
stone line. They commonly show a saprolitic composition with higher SiO2 contents and are
deposited on the laterite surface. Very often termites carried this material upwards from deeper
horizons. In other instances zirkonium contents in the surface horizons of laterite (nickel
limonite) above ultramafic rocks indicate an admixture from areas with other parent rocks.

Chemical alterations and differences in lateritization

All laterites are marked by an enrichment of iron and a decrease of silica together with the highly
soluble alkalis and alkaline earths. But apart of these characteristics the composition and
properties of laterites can be quite different and are strongly controlled by the chemical and
physical features of the parent rock. Above all the behaviour of aluminium is not uniform. In
essence two principal groups can be distinguished:
- Laterites on mafic (basalt, gabbro) and on ultramafic rocks (serpentinite, peridotite, dunite).
These rocks are free of quartz and show lower silica and higher iron contents.

- Laterites on acidic rocks. In this group not only granites and granitic gneisses but also many
sediments as clays, shales and sandstone shall be included. These rocks contain quartz and have
higher silica and lower iron contents.

The following table shows main element percentages of rocks from these two groups and their
corresponding laterites. The cited percentages are typical average values of numerous laterite
samples and their parent rocks which were collected by the author in many tropical countries.

SiO2 Al2O3 Fe2O3 Fe2O3 : Al2O3

Laterite 46,2 24.5 16.3 0.67

Granite 73.3 16.3 3.1 0.19

_____________________________________________________________

Laterite 39.2 26,9 19.7 0.73

Clay 56.5 24.4 5.3 0.22

_____________________________________________________________

Laterite 23.7 24.6 28.3 1.15

Basalt 47.9 13.7 14.9 1.09

_____________________________________________________________

Laterite 3.0 5.5 67.0 12.2

Serpentinite 38.8 0.7 9.4 14.1

The laterites formed above these rocks do not only show divergent chemical compositions but
also contrasting physical properties. The very ferruginous yellowish brown laterite (nickel
limonite) on serpentinite is generally soft and displays a very fine porosity, indicated by a low
bulk density. In few occurences a hard cuirass has formed at the surface by dissolution and
reprecipitation of iron. Also the laterites on basalts are commonly soft and friable. They are
intensively redbrown coloured and form relatively fertile soils. The laterites on acidic rocks
behave quite differently. They frequently show a typical sequence with a pallid zone (saprolite),
a mottled zone and a darkbrown laterite on top which is often described. These laterites harden
after drying which often allows their application as brickstones.
Genetically most relevant, however, are the differences in the Fe2O3 : Al2O3 ratios. Laterites on
mafic and ultramafic rocks show generally similar ratios as the underlying parent rock. This can
be easily interpreted by the loss of soluble elements causing an equivalent accumulation of the
residual elements iron and aluminium which corresponds with the classic interpretation of
laterite formation. On the other hand, laterites on acidic rocks show generally strongly increased
Fe2O3 : Al2O3 ratios. There are only two explanations for this difference:

- Iron is introduced into the laterite from outer sources (absolute iron accumulation). The
difficulties of absolute iron accumulation on a larger scale were already discussed. Moreover, it
is inexplicable that an introduction of iron is only active in lateritization of acidic and not of
mafic and ultramafic rocks.

- If absolute iron accumulation can be ruled out as a dominant factor, only a residual
concentration can be quoted. This is particular strong if also aluminium together with silica is
lost in solution resulting in highly increased Fe2O3 : Al2O3 ratios.

If aluminium would not be removed in the course of lateritization of acidic rocks, bauxites
should commonly form on these widespread rocks because of their high Al2O3 : Fe2O3 ratios.
But actually bauxites are rare compared with laterites. They are restricted to areas with
exceptionally good leaching conditions which allow partial (incongruent) kaolinite dissolution
with subsequent formation of gibbsite due to a very low concentration of dissolved silica. Under
weaker leaching conditions gibbsite does not form or forms only in minor quantities. This is
favoured by the presence of quartz and the lower permeability of weathered acidic rocks
compared with the more porous and friable laterites on mafic and ultramafic rocks.

What is the reason for a stronger (residual) iron accumulation under comparatively weaker
leaching conditions which might be paradox at the first sight? The author suggests the cause in
the dissolution and neoformation of kaolinite , of wich two generations were observed in many
laterite samples. In a first generation kaolinite replaces the silicate minerals of the parent rock
which already occurs in the saprolite stage. In a second generation very fine-grained and iron-
stained kaolinite with lower crystallinity fills small voids and fissures in the lateritic matrix.The
two laterite generations can clearly be observed in laterite thin sections (see the last photo in the
link with attached images). This secondary kaolinite increases with proceeding lateritization. Its
occurence in open spaces shows precipitation from soil solution. Dissolution and neoformation
of kaolinite proceed at different times and at different places in the lateritic profile, depending on
the specific chemical and physical conditions in the respective microenvironment.The same
kaolinite sequence was observed by Balan et al (2007) in a recent study of a lateritic profile
above kaolinitic clays in Brazil. The well ordered primary kaolinite of sedimentary origin
decreased in the lateritic profile with decreasing depth, accompanied by a rising fraction of
poorly ordered, neoformed kaolinite. An impregnation with finely divided, gel-like secondary
kaolinite might be the cause for the hardening properties of many laterites on acidic rocks which
enable their use as brickstones and are not encountered in laterites on mafic (basaltic) rocks.
Detailed microprobe analyses by the author of various laterite samples only proved the well-
known laterite minerals and no amorphous compounds with variable composition which might
equally cause hardening after drying.
The author concludes that substantial amounts of dissolved Al and Si, originating from the
congruent dissolution of primary kaolinite, are not re-precipitated in the secondary kaolinite but
are removed with the percolating water. Waters originating from laterite areas have normally a
neutral pH which excludes substantial Al amounts in true solution. Moreover, dissolved Al could
not be proved by conventional analyses of filtered waters. Therefore it can be presumed that
removal of Al takes place in form of larger Al-Si-compounds probably of colloidal size. This is
promoted by kinetic factors especially by the extremely slow reaction rate of kaolinite formation
which allows removal of Al and Si even in the stability field of kaolinite. Furthermore, colloidal
mobilization of Al and Si is proved by informative short-time dissolution experiments with
kaolinitic oxisols (Malengreau and Sposito (1997). Colloidal particles of kaolinite and
amorphous silica were released in solution after dissolution periods of 1-12 h at pH 2-6.

Mobilization of aluminium could be clearly demonstrated by McFarlane and Bowden (1992)

who analysed in detail soil and water samples from a toposequence in Malawi. Al and Si are
released by congruent kaolinite dissolution in lateritic interfluve areas and re-precipitated in the
neighboured bottomland in form of various alumo-silicates. Waters from wells and boreholes
were analyzed after different treatments and show substantial amounts of Al if the samples were
not filtered and acidified prior to analysis, whereas filtration diminished the Al content
strongly. The authors conclude that dissolution of kaolinite is promoted by micro-organisms and
the released Al is mobilized together with Si in organically bound form. They stress that
mobility is not synonymous with solubility.

The presented analyses and observations led the author suggest a three-step-model of tropical
weathering, depending on the intensity of the weathering processes:

- Weaker tropical weathering gives rise to formation of saprolites which are the prevailing
weathering products in the tropics and are frequently misinterpreted as laterites.

- Advanced tropical weathering results in the formation of most of the laterites showing a
much stronger residual enrichment of Fe as against Al. A higher tropical rainfall and
a moderate drainage together with the presence of quartz are generally not sufficient for a
pronounced incongruent kaolinite dissolution and a pronounced formation of gibbsite. As
already discussed in this article, Al- and Si-bearing compounds of probably colloidal size are
thus removed from the weathering mantle in high quantities. Laterites formed in this way are
frequently indurated and predominate in the tropics above clays, shales, granites and granitic
gneisses. Friable laterites with high contents of iron oxides and kaolinite form on basaltic rocks.

- Strong tropical weathering is promoted by a very pronounced rainfall, a deep ground water
level and a high permeability of the weathered rock, allowing an excellent drainage which is
essential for the formation of bauxites (Bardossy and Aleva, 1990) These factors cause an
incongruent dissolution of kaolinite with formation of gibbsite. The composition of the laterite is
determined by the composition of the parent rock. The most widespread acidic rocks with their
high Al- and Si- and their low Fe-content give rise, in favourable cases, to formation of high
grade-bauxites. Ferruginous bauxites of a relatively poor quality form on basaltic rocks.
Ultramafic rocks are transformed in thick deposits of a very ferruginous laterite (nickel limonite
ore) which frequently covers nickel silicate ore.
Economic relevance

Lateritic weathering has a considerable economic significance above all for the mining of
relevant metals predominantly nickel and aluminium.

Nickel laterites supply presently 44 % of the world nickel production and constitute 73 % of the
continental resources. In the near future they will obtain the first position also in the production.
The ores are bound on ultramafic rocks above all serpentinites which consist largely of the
magnesium silicate serpentine containing approx. 0.3 % Ni. This mineral is nearly completely
dissolved in the course of lateritization leaving behind a very iron-rich, soft residue in which
nickel is concentrated up to 1 - 2 % Ni (for main element percentages see the proceeding table).
The bulk of this so-called nickel limonite or nickel oxide ore consists of the iron oxide goethite
in which nickel is incorporated. Therefore it cannot be concentrated physically by ore dressing
methods.

Below the nickel limonite another type of nickel ore has formed in many deposits. This is called
nickel silicate ore which consists predominantly of partially weathered serpentine. It is depleted
in magnesium and forms with 1.5 2.5 % Ni the most relevant type of lateritic nickel ores. In
contrary to the relatively enriched limonite ore, the nickel silicate ore owes its nickel content to a
process of absolute nickel enrichment. The nickel is leached downwards from the overlying
limonite zone since not all of the nickel, which is released from the serpentinite in the course of
nickel limonite formation, can be incorporated in goethite and therefore cannot be fixed in the
limonite zone. The downward migrated excess nickel is incorporated in the Mg-depleted
serpentine and occasionally in neo-formed clay minerals predominantly smectite. Some deposits
show admixtures and layers of secondary quartz which is precipitated from weathering solutions
supersaturated in Si, due to a rapid dissolution of serpentine.

A third type of lateritic nickel ore is garnierite which is found in pockets and fissures of the
weathered ultramafic rocks. The green garnierite ore containing mostly 20 40 % Ni consists of
a mixture of the phyllosilicates serpentine, talc, chlorite and smectite in which a high percentage
of magnesium is substituted by nickel. It is also formed by downward nickel leaching and
precipitation in hollow spaces of the weathered rock. Today, nickel silicate ores with high
portions of garnierite are largely exhausted. Important deposits of nickel laterite are located in
many tropical countries above all in New Caledonia.

Bauxites are almost the only source for the production of aluminium. There is no principal
difference between laterites and bauxites since bauxites are nothing else than highly aluminous
varieties of laterite showing continuous transitions. Bauxites largely consist of the Al-minerals
gibbsite Al (OH)3, boehmite and diaspore AlOOH together with the iron oxides goethite and
hematite, the clay mineral kaolinite and small amounts of anatase. In commercial bauxites the
kaolinite content must be low. Bauxite was named after the French village Les Baux-de-
Provence where it was first discovered.

In geosciences lateritic bauxites (silicate bauxites) are distinguished from karst bauxites
(carbonate bauxites). The early discovered karst bauxites occur predominantly in Europe and
Jamaica on karst surfaces of limestone. They also formed by lateritic weathering of silicates
either from intercalated clay layers or of clayey dissolution residues of the limestone. These
bauxites frequently contain boehmite and diaspore in addition to gibbsite. The bauxites in
Jamaica rest on tertiary limestone and are exposed at the surface whereas the European bauxites
are bound on older carbonate rocks of jurassic and cretaceous age. If they are covered by
younger sediments they have to be mined underground. Their contribution to the world bauxite
production is today relatively small.

Most dominant are nowadays the tropical silicate bauxites which are formed at the surface of
various silicate rocks such as granites, gneisses, basalts, syenites, clays and shales. As already
discussed, the formation of bauxites demands a stronger drainage as laterite formation to enable
precipitation of gibbsite which is the prevailing aluminium hydroxide in lateritic bauxites. Zones
with highest Al contents are frequently located below a ferruginous surface layer and are due to
downward leaching of aluminium which is more soluble than iron under oxidizing conditions.
Near the parent rock interface gibbsite frequently replaces primary minerals predominantly
feldspars which results in a preservation of the primary rock structure.

Large deposits of lateritic bauxites with a high production are in Australia, Brazil, Guinea and
India together with Guyana, Suriname and Venezuela.

High grade iron ores on top of tropical deposits of banded iron formations (BIF) are also
attributed to lateritic weathering which causes dissolution and removal of siliceous constituents
in the banded iron ore.

Lateritization processes are equally relevant for the alteration of gold deposits. In the tropics the
laterite cover around outcropping gold-quartz-veins often shows a pronounced gold dispersion
halo which can be traced by geochemical exploration. It is proved that the primary gold is
partially moved in solution and re-precipitated in secondary gold particles with lower grain size
and reduced Ag content. Locally also the secondary lateritic Au mineralization is workable.

The importance of laterite as building material has already been mentioned. More relevant as
their local use for the construction of simple houses is their application as a road building
material. The suitability of lateritic materials above all of lateritic gravel is tested by several
methods of engineering geology.

The significance of lateritization for agriculture is not positive since strong leaching results in
the impoverishment also of nutrients in lateritic soils. Moreover the hardening properties of
many laterites complicate agriculture. Only the friable red-brown lateritic soils on basaltic rocks
enable good crops.

This article is intended to present a general view on laterite. It considered a great number of
publications which can hardly be cited here (see Monographs). Some interpretations of the
numerous scientific results in the laterite literature reflect the personel viewpoint of the author.

References
Balan E. et al. (2007): Inheritance vs. neoformation of kaolinite during lateritic soil formation: A
case study in the middle Amazon basin. Clays and Clay Minerals 55, 253-259.

Bourman, R.P. and Ollier ,C.D. (2002): A critique of the Schellmann definition and classification
of laterite. Catena 47, 117-131.

McFarlane, M. J. and Bowden, D. J. (1992): Mobilization of aluminium in the weathering

profiles of the African surface in Malawi. Earth Surface Processes and Landforms 17, 789-805

Malengreau, N. and Sposito, G. (1997): Short-time dissolution mechanisms of kaolinite tropical

soils. Geochom. Cosmochim. Acta 614297-4307.

Schellmann, W. (1986): A new definition of laterite: Geol. Survey India Memoirs 120 1-7.

Monographs

Aleva, G.J.J. (Ed.) (1994): Laterites. Concepts, Geology, Morphology and Chemistry. 153 p.
ISRIC, Wageningen, ISBN 90-6672-053-0

Bardossy, G. and Aleva, G.J.J. (1980): Lateritic Bauxites. 624 p. In: Developments in Geology
27, Elsevier, Amsterdam, ISBN 0-444-98811-4.

Tardy, Y. (1997): Petrology of Laterites and Tropical Soils. 419 p. ISBN 978-9054- 106784

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Author: Dr. Werner Schellmann studied Mineralogy at the University of Marburg and was
employed 1958 -1991 at the Bundesanstalt fr Geowissenschaften und Rohstoffe (Federal
Institute for Geosciences and Natural Resources) in Hannover, Germany. He was predominantly
engaged in the research of laterites, bauxites and lateritic nickel ores which were studied in many
countries in the tropical world. The results were published in numerous papers.