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1
SAC 101
❖ The term SOIL was derived from the Latin Word “SOLUM” Means FLOOR
❖ For a Layman soil is dirt or debris
❖ For a Mining Engineer soil is a debris covering the Rocks
❖ For a Civil Engineer soil is a material on which road or house bed is formed
❖ For a Home Owner soil is a mellow or loamy or hard material
❖ For an Agriculturist soil is a medium for plant growth
❖ Whitney (1892):Soil is nutrient bin which supplies all nutrients required for plant growth.
❖ Hilgard (1892): Soil is more or less a loose and friable material
❖ Dokuchaiev (1900): Father of soil science - Soil is a natural body composed of mineral
and organic constituents
❖ Joffe (1936): Soil is a natural body of mineral and organic constituents differentiated into
horizons
❖ Jenny (1941): Soil is a naturally occurring body formed due to combined influence of
climate and living organisms acting on parent material
❖ Soil Science Society of America (1970): (i) Soil is the unconsolidated mineral matter
influenced by genetic and environmental factors (ii) The unconsolidated mineral material
on the immediate surface of the earth that serves as a natural medium for the growth of
land plants.
❖ SOUL OF INFINITE LIFE (SOIL) - J.S. Kanwar
❖ Soil is a three dimensional body having length, breadth and depth.
❖ Composition of soil on volume basis: Mineral matter: 45%, Organic matter: 5%, Soil
water: 25%, Soil air: 25%
❖ Study of origin of the soil, its classification and its description (Pedology)
❖ Study of Soil from the stand point of higher plants (Edaphology)
❖ Soils consist of four major components: mineral matter, organic matter, soil air & soil
water
❖ Soil a three phase system: solid particles, water and air
❖ Out of 106 elements known, 8 are sufficiently abundant as to constitute about 99(%) by
weight of the earth’s crust (up to 16 km)
❖ Oxygen: 46.6 %, Si: 27.72%, Al: 8.13%, Fe: 5.00%, Ca: 3.63%, Na: 2.83%, K: 2.59,
Mg:2.09 %
❖ A rock may be defined as a hard mass of mineral matter comprising two or more rock
forming minerals.
❖ Petrology deals with science of rocks.
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SAC 101
❖ Petrography which deals with description of rocks.
❖ Petrogenesis which is the study of origin of rocks.
❖ Composition of Earth’s crust as a whole: Igneous rocks (95%); Sedimentary rocks- 5%
(Shale-4%, sandstone- 0.75%, limestone- 0.25%)
❖ Composition of the upper 5 km of the Earth’s crust: Sedimentary rocks- 74 % (Shale-
52%, sandstone- 15%, limestone- 7%); Igneous rocks- 18 % (Granite- 15%, Basalt- 3
%)
❖ Cooling and consolidation of molten magma within or on the surface of earth Igneous/
Primary rocks/Massive rocks
❖ Disintegration and decomposition lead to breaking down & Transportation and
cementation of pre-existing rocks- Sedimentary/ Secondary rocks/ Stratified rocks
❖ The primary and secondary rocks when subjected to earth’s movement and to high
temperature and pressure are altered to new rocks called Metamorphic rocks
❖ Based on mode of origin igneous rocks are Extrusive rocks & Intrusive rocks
❖ The consolidation of magma on the surface of the earth- Extrusive rocks (or volcanic
rocks) eg. Basalt- fine textured
solidification of magma below the surface of the earth- Intrusive rocks (or plutonic rocks)
eg. Granite- Coarse textured
❖ Based on mode of chemical composition igneous rocks are
• Acid rocks : > 65% silica (Granite, rhyolite)
❖ Sediments may contain various size particles cemented together by substances like SiO2,
Fe2O3 or lime- Clastic rocks
❖ Based on the origin sedimentary rocks- Residual (Laterite) & Transported
❖ Deposited as solids in suspension: Sandstone, shale
❖ Deposited by chemical precipitation: Limestone, ironstone
❖ Deposited through agency of organic matter: Peat, Phosphatic deposits
❖ Based on the grain size sedimentary rocks are classified as
❖ Rocks with boulder pebbles sized minerals (Rudaceous) : Conglomerate
❖ Rocks with sand size particles (Arenaceous): Sandstone
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SAC 101
❖ Rocks with silt size particles (silt rocks) : Siltstone
❖ Rocks with clay size particles (Argillaceous) : Shale
❖ The changes due to water is called hydrometamorphism
❖ The changes due to heat is thermometamorphism
❖ The changes due to pressure are called dynamometamorphism.
❖ The metamorphic rocks formed from, Sand stone: Quartizite, Shale: Slate/mica, schist,
Lime stone: Marble, Granite: granite gneiss, Dolerite: Hornblende gneiss
❖ Primary minerals: original components of rocks (feldspar, mica)
❖ Secondary minerals: Minerals that are formed from changes in primary minerals and
rocks (clay minerals)
❖ CLAY- most reactive part of soil
❖ Essential minerals: chief constituents of rocks (Feldspars, pyroxenes, micas )
❖ Accessory minerals : present in small quantities, whose presence or absence will not
alter properties of rocks (tourmaline, magnetite)
❖ Essential minerals of Granite (Quartz (20 to 30%)), Syenite (Quartz, orthoclase), Diorite
(Quartz), Gabbro (Labradorite, augite, olivine), Dolerite (Labradorite, augite, olivine),
Basalt (Labradorite, augite, olivine)
❖ Primary minerals- Ferro-magnesium minerals & Non-ferromagnesium minerals
❖ Ferro-magnesium minerals- ortho-inosilicates (16.8 %) & Phyllosilicates (3.6 %)
❖ Only ferro-magnesium minerals without Fe & Mg- Muscovite
❖ Ortho silicates- Isolated tetrahedron (olivine)
❖ Inosilicates- SINGLE chained- 2 oxygen ions shared (Pyroxene); DOUBLE chained- 2/
3 oxygen ions shared (Amphiboles)
❖ Phyllosilicates/Layer/Sheet silicates: 3 oxygen ions shared - 2 dimensional- Honey
comb structure. Biotite/ black mica & Muscovite/ white mica
❖ Tectosilicates (Non-Ferro Magnesium): 4 oxygen ions shared, 3-d structure,
Framework/Network silicates; Feldspar [61 %] (orthoclase, Plagioclase) & Quartz
❖ Orthoclase (Potassic feldspar); Plagioclase (Albite- Na feldspar; Anorthite- Ca feldspar)
❖ Dominant element in Earth’s crust is oxygen
❖ 2nd dominant element in Earth’s crust is Silicon
❖ Dominant metallic element in Earth’s crust is Aluminium
❖ Dominant mineral in Earth’s crust is Feldspars
❖ Second most abundant mineral next to feldspars is Quartz (most resistant to weathering)
❖ Non-silicate minerals: oxides (Haematite, Limonite, Goethite, Gibbsite); Carbonate
(Calcite, Dolamite); Sulphates( Gypsum); Phosphates (Apatite)
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SAC 101
❖ Red colour of soil due to presence of Haematite
❖ Yellow colour of soil due to presence of Limonite
❖ Clay minerals are of size <0.002 mm/ 2 micrometer
❖ 1 silicon tetrahedron + 1 aluminium octahedron = 1:1 clay mineral (Kaolinite, halloysite,
anauxite and dickite)
❖ Kaolinite- Simplest mineral among all, Dominant clay mineral in red and laterite soils, 2
sheets of each crystal unit held together by oxygen bonding atoms- Units are held
together very rigidly by hydrogen bonding
❖ 2 (silicon tetrahedron) : 1(aluminium octahedron) expanding clay mineral= Smectite
group: montmorillonite, beidellite, nontronite and saponite
❖ Montmorillonite- crystal units are held by very weak oxygen – oxygen linkages; High
swell-shrink capacity among all clay minerals
❖ 2:1- vermiculite (limited/partially expanding)- Weathered product of mica- Potassium
(K) – replaced by exchangeable magnesium (Mg) ion
❖ Vermiculite - high (negative charge &, CEC, layer charge, surface area) among all
clay minerals
❖ 2 : 1 non-expanding clay mineral= Illite/Hydrous mica (15 % Si in silica sheets is
substituted by Al)- Excess negative charge is satisfied by- K
❖ 2 (silicon tetrahedron) : 1 (aluminium octahedron) : 1 (Mg octahedron- Brucite sheet)
clay mineral= 2:2 or 2:1:1- Chlorite
❖ Clay minerals dominant in Alluvial soil (Illite); Red and lateritic soil (Kaolinite); Black
soils (Smectite- Montmorillonite); Desert soils (Illite & Attapulgite);
❖ Amorphous minerals: Para-crystalline, Allophane, imogolite
❖ Smallest size among clay minerals- Montmorillonite (0.01-1.0 microns)
❖ Largest size among clay minerals- Kaolinite (0.1-5.0 microns)
❖ CEC- lowest for Kaolinite (3-15 Cmol (P+) kg-1); highest for Vermiculite (80-150 Cmol
(P+) kg-1
❖ Weathering is breakdown and alteration of rocks and minerals at or near Earth's surface
by a set of physical, chemical and biological processes.
❖ Weathering results in the formation of Regolith or Parent material
❖ Regolith is an unconsolidated residual mass of weathering rock
❖ Parent material: It is regolith or at least its upper portion from which soils are developed.
❖ Physical weathering refers to disintegration and breaking down of rocks, without
producing any new substances.
❖ Rock → Weathering → Regolith → soil forming factors and processes → True soil
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SAC 101
❖ Diurnal temperature changes causes peeling off the surface layers from the rocks
(“Exfoliation” or onion type of weathering) Eg: Basalt & Granite
❖ Cold temperature causes freezing of entrapped water inside the rock which expands 9% in
volume & exerts pressure of 1465 tonnes/m2
❖ Water acts as a disintegrating, transporting and depositing agent
❖ Frost is much more effective than heat in producing physical weathering
❖ The shifting of soil causes serious wind erosion problem and may render cultivated land as
degraded (e.g) Thar desert of Rajasthan
❖ Some natural substances increase considerably in volume on wetting and shrink on
drying. (e.g.) smectite, montmorillonite
❖ Decomposition of rocks and minerals by various chemical processes is called chemical
weathering
❖ Hydration refers to chemical combination of water molecules with a particular substance
or mineral leading to a change in structure
❖ Hydrolysis is the most important process in chemical weathering among all- type of
double decomposition process- forerunner of clay formation
❖ Hydrolysis results in complete disintegration & drastic modification of primary
minerals
❖ Oxidation is process of addition and combination of oxygen to minerals.eg Haematite to
Limonite
❖ Carbonation: Carbon di-oxide when dissolved in water it forms carbonic acid
❖ Some substances present in the rocks are directly soluble in water- Solution (Halides)
❖ Reduction is process of removal of oxygen and addition of electrons
❖ Weathering sequence- Quartz (most resistant) > muscovite > K feldspar > Na and Ca
feldspar > biotite, hornblende, augite > olivine > dolomite and calcite > gypsum (least
resistant)
❖ Biological Weathering is both decomposition and disintegration of rocks and minerals
❖ Dokuchaiev (1889) established soil forming factors viz., S = f ( p, cl, o )
❖ Jenny (1941) added two more factors i.e., relief & time- S = f (cl, o, r, p, t, …)
❖ J.S. Joffe classified into Active and Passive factors
❖ Active soil forming factors: i) Climate, ii) organism (vegetation or biosphere)
❖ Passive soil forming factors: i) Parent material, ii) Relief, iii) Time
❖ Sedimentary: Formed in original place. It is the residual parent material.
❖ Colluvium: It is the poorly sorted materials transported by the action of gravity
❖ Alluvium: The material transported and deposited by water
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SAC 101
❖ Moraine : Transported and deposited through the action of glacial ice
❖ Lacustrine: Transported and deposited through the lake water
❖ Aeolian (sandy texture) ; Loess (silty texture): Transported and deposited through wind
❖ These soils develop under the influence of parent material is Endodynamomorphic
soils
❖ Development of normal profile under influence of climate and vegetation is Ecto
dynamomorphic soils
❖ Acid igneous rocks (granite, rhyolite) produce light-textured soils (Alfisols).
❖ Basic igneous rocks (basalt), alluvium or colluvium derived from limestone or basalt,
produce fine-textured cracking-clay soils (Vertisols).
❖ Si and Al forms the skeleton for production of secondary clay minerals.
❖ Fe and Mn are important for imparting red color to soils and for oxidation and reduction
phenomena.
❖ Na and K are important dispersing agents for clay and humus colloids.
❖ Ca and Mg have a flocculating effect- favorable and stable soil structure for plant
growth
❖ The period taken by given soil from stage of weathered rock (i.e. regolith) up to stage of
maturity is considered as time
❖ The time that nature devotes to the formation of soils is termed as Pedologic Time
❖ Weathering stages in soil formation- Initial- Juvenile- Verile- Senile- Final
❖ The matured soils mean soils with fully developed horizons (A, B, C)
❖ Arid climate- formation of saline soils; cool humid climate- Podzols- warm humid
climate- Laterite soils
❖ Van’t Hoff law “with every 10 ˚C rise in temperature, speed of chemical reaction
increase by factor of two or three
❖ Soils formed from same parent material but differ in topographic positions- show
differential profile development- sequence of such soils termed as toposequence
❖ Soil catena- term introduced by G. Milne – sequence of topographically related soils
have comparable parent material, climate and age but, different soil characteristics due to
variation in relief
❖ Jenny (1941)- tropical regions rate of weathering proceeds three times faster than in
temperate regions and nine times faster than in arctic
❖ Jenny (1941) defined parent material as “Initial stage of soil system”
❖ Basic soil forming processes- Simonson’s fourfold forming process- Addition, Losses,
Transformation and Translocation
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SAC 101
❖ Fundamental processes of soil formation- Eluviation, Illuviation and Humification
❖ Eluviation (Emigration) - mobilization & translocation of certain constituent’s viz. Clay,
Fe2O3, humus, salts etc- “Washing out”- Horizon formed (A2 or E horizon)- “Zone of
leaching”
❖ Illuviation (Immigration)- Process of deposition of soil materials- horizon (Bt)-
“Washing in”- “Zone of accumulation”
❖ Humification- Process of transformation raw organic matter to humus
❖ Specific Soil farming processes- Calcification, Decalcification, Laterization, Salinization-
Desalinization, Alkalization, Dealkalization, Calcification, Decalcification, Gleization,
Pedoturbation
❖ Podzolization- Process of soil formation resulting in formation of Podzols soils-
accumulation of silica- “Acid leaching”- Negative of calcification
❖ Laterization/latozation - “Alkaline leaching”- Accumulation of sesquioxides- removal of
silica
❖ Salinization- process of accumulation of salts like sulphates & chlorides of Ca, Mg, Na
& K in soils- salic horizon- develop- Solonchaks/ saline soils- EC > 4 dS m-1
❖ Desalinization- process of removal by leaching of excess soluble salts from horizons
❖ Solonization or Alkalization- accumulation of sodium ions on exchange complex of
clay- Solonetz soils
❖ Solodization/ dealkalization: process removal of Na+ from exchange sites
❖ Calcification: accumulation of calcium carbonate (CaCO3)- Calcic horizon
❖ Gleization: process development of glei (gley horizon)- poor drainage condition-
Hydromorphic soils
❖ Pedoturbation- process of mixing of soil
❖ Argillic pedoturbation- Mixing of soil by churing process caused by swell shrinking of
clays
❖ Horizonation: process of differentiation of soil in different horizons
❖ Soil horizon: vertical section of soil showing various layers from surface to unaffected
parent material
❖ Soil is made up of distinct horizontal layers; these layers are called horizons.
❖ Master horizons are O, A, E, B and C horizons
❖ O horizon is topmost layer of most soils
❖ A horizon zone of translocation- eluviation
❖ B horizon(“Sub-soil”) is a mineral soil layer which is strongly influenced by illuviation-
enrichment of clay particles
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SAC 101
❖ C horizon is composed of weathered parent material- least affected by weathering
❖ R horizon (Bed-rock horizon): Deepest horizon/ final layer in soil profile- consists of
unweathered bedrock.
❖ A pedon is smallest volume that can be recognized as a soil individual, area (1 to 10 m2)
❖ Polypedon is defined as a continuous similar pedons-minimum area > 1 km2
❖ Regolith: unconsolidated materials above parent rock including A, B and C horizons
❖ A and B horizons are called as Solum
❖ Soil texture- Relative proportion of sand, silt and clay- cannot be easily altered
❖ Size of clay <0.002mm (all systems clay size same); Silt - 0.002 – 0.02mm; Fine sand-
0.02 – 0.2mm; Coarse sand- 0.2 – 2.0 mm by USDA
❖ SAND AND SILT forms Skeleton; Flesh of Soil is CLAY
❖ Stokes' Law: " Velocity of a falling particle is proportional to square of radius and not to
its surface”
❖ Sandy soil- at least 70 % sand separate; Loamy soil- equal proportion of sand, silt &
clay (ideal soil for crop production)
❖ Clayey soils must contain 35 % of clay. Silty soils- at least 80 % of silt
❖ Textural classes are 12: Sandy, Loamy sand, Sandy loam, Loam, Silt loam, Silt, Sandy
clay loam, Clay loam, Silty clay loam, Sandy clay, Silty clay and Clay
❖ Heavy soil- fine textured soils (clay soil); Light soil- coarse textured soils (sandy soils)
❖ The international pipette method- standard method for particle size analysis
❖ Peds: Natural aggregates
❖ Clod is an artificially formed (due to ploughing, digging etc.) soil mass
❖ Categories of soil texture- “Type, Class & Grade”
❖ Type -Shape or form and arrangement pattern of peds; Class-Size of Peds; Grade-
Degree of distinctness of peds
❖ Type (4) : Platy, prismatic, blocky & spheroidal; Class (5): Very fine, Fine, Medium,
Coarse and Very coarse; Grade (4): Structure less, Weak, Moderate and Strong
❖ Platy- Aggregates are arranged in relatively thin horizontal axis (thick units- platy; thin
units- laminar)
❖ Prism-like: vertical axis is more developed than horizontal (tops clear cut- Columnar;
tops are rounded- Prismatic)
❖ Block like: All three dimensions are about same size (Angular- faces flat & edges sharp;
sub angular blocky- faces and edges rounded)
❖ Spheroidal: All rounded aggregates; (Crumby- granules high porous; Granular-
granules less porous); Crumby well suited structure for agriculture
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SAC 101
❖ For naming a soil structure sequence followed is grade, class and type
❖ Soil structure can be modified by cultivation and tillage while texture is an inherent
property of soil and cannot be modified within short period of time
❖ Soil Bulk Density(BD)(Mgm-3) measures total soil volume, Mass/volume of wet or dry
soil. (“Apparent specific gravity”)
❖ Soils loose, porous, or well-aggregated will have lower bulk densities than soils that are
compacted or non-aggregated.
❖ BD of sandy soils vary between 1.2 to 1.8 Mg m-3
❖ BD of Fine-textured soil, Clays, silty clays, or clay loams,- 1.0 and 1.6 Mg m-3
❖ Increase in pore space, organic matter, clay content, primary tillage, decreases BD
❖ Particle Density (“True density”)- Mass/ volume of soil solids only- texture & structure
do not affect
❖ Soils high in organic matter have lower particle densities
❖ Particle density of mineral soils is assumed to be 2.65 Mg m-3\
❖ BD include both pore space & solid space; PD include only solid space
❖ Pore-spaces (voids) in soil is portion of soil volume not occupied by soil solids
❖ % Pore space/ porosity= (1-BD/PD x 100)
❖ Crumby & granular structure more pore spaces than other soil structure
❖ Total pore space (porosity) is high for clay soils than sandy soil
❖ Soil containing high organic matter possesses high porosity
❖ Size of macro pores >0.08 mm; micro / capillary pores <0.08 mm
❖ Kinds of soil color- Lithochromic & pedochromic/ acquired
❖ Lithochromic- inherited from its parent material, red soils from red sandstone
❖ Pedochromic- develops during soil formation through different soil forming processes,
Eg: red soils from granite or schist
❖ Organic matter- dark brown or black; soils with dominant of Haematite- red color;
Goethite- yellow; Glaucoite- green; Calcite- whitish
❖ Soil colors are best determined by comparison with Munsell Colour Chart (199 color
chips)
❖ Hue - dominant spectral color (redness or yellowness)
❖ Value- relative lightness or darkness of a color (amount of reflected light), scale (0-10)
❖ Chroma - purity of the color (strength of color) scale (0-8)
❖ Soil color is one of the most useful- identification and classification of soils, distinguish
different horizons of a soil profile, indicator of soil moisture regimes
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SAC 101
❖ Soil consistence is resistance of a soil at various moisture contents to mechanical
stresses
❖ The range of soil moisture content under friable condition is optimum for tillage
❖ ‘Cohesive’ and ‘adhesive’ forces, which determine ease with which soil can be reshaped
or ruptures
❖ Plasticity of soil is capacity to be molded and to retain shape even when stress is removed
❖ Soils containing > 15% clay exhibit plasticity
❖ The three limits (indices) of plasticity: shrinkage limit or lower plastic limit, ii) plastic
limit and iii) liquid limit or upper plastic limit
❖ The moisture content at which soil ceases to be plastic, becomes semi-fluid and tends to
flow like a liquid is upper plastic limit
❖ It is soil moisture content below which soil becomes friable; soil water mass is unable to
change shape continuously under applied force- lower plastic limit
❖ Plasticity number (Index)- The difference between moisture content (consistency) of
upper and lower plastic limits.
❖ Soil with expanding type clay- high liquid limit & plasticity index- Organic matter favors
plasticity
❖ Na saturated soils have lower plastic limits than K, Ca and Mg saturated soils
❖ pF values- lower plastic limit- 2.8 – 3.2; and upper plastic limit- 0.5
❖ Physical classification of soil water- i) Gravitational water ii) Capillary water and iii)
Hygroscopic water
❖ Gravitational water- “free water” occupies larger soil pores (macro pores) and moves
down readily under force of gravity.
❖ Soil moisture potential at gravitational state is 0 or > - 1/3 bar
❖ Capillary water is held in capillary pores (micro pores)- It is held at potential -1/3 bar to
-31 bar
❖ Hygroscopic water: water that held tightly on surface of soil colloidal particle- moves in
form of water vapor- held in soil at potential of > -31 bar
❖ Plants cannot absorb this water (unavailable), certain microorganism may utilize
hygroscopic water
❖ Gravitational water and Hygroscopic water unavailable to plants; but part of Capillary
water is available to plants
❖ Biological Classification of Soil Water: Available, unavailable & Super available or
superfluous water
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SAC 101
❖ Available water: Portion of water retained in soil between field capacity (-1/3 bar) and
permanent wilting coefficient (-15 bars)- easily usable by plants
❖ Un-available water: water held in soil at potential > -15 bar - unavailable to plants-
includes whole of hygroscopic water & part of capillary water
❖ Superfluous water: Water which is retained in soil beyond field capacity soil moisture
tension- Includes gravitational water + portion of capillary water- unavailable to plants
❖ 0 to - 0.3 bar = Gravitational; - 0.3 bar = Field Capacity; -15 bar = wilting point;
Between -0.3 to -15 bar plant available water; -15 to -100 bar = stages of air dry; -10,000
bar = oven dry
❖ pF Scale (Schofield)- height of water column (cm) to give necessary suction- free energy
measured in terms of height of water column to produce suction
❖ pF value at field capacity- 2.53; Wilting point- 4.18; Hygroscopic point - 4.50
❖ Gravimetric method (direct method): simple, most accurate & most widely used
method- drying it in an oven at 105°C- reliable, unaffected by salt content; disadvantage-
very time consuming, laborious
❖ Electrical conductivity method (Gypsum block method): % moisture from field
capacity to wilting point- affected by salt concentration in soil solution
❖ Neutron scattering method: Fast neutrons are emitted by neutron emitters like radium-
beryllium or americium-beryllium- detector consists of Boron tri-fluoride gas (BF3)
❖ Time Domain Reflectometry- Based on “dielectric constant of water”- as water content
increases, dielectric constant increases- independent of soil texture, temperature & salt
content
❖ Gamma ray attenuation method: Consists to two “Al” tubes- one tube- radioactive
isotope (Caesium-137) & other tube- thallium-activated NaI crystal as detector- follows
principle of Beer’s law
❖ Field Tensiometer (suction method): measures matric potential - confined up to
minimum matric potential of -0.85 bar
❖ Soil Water Potential: Measure of energy status of soil water to do some work (unit: bars
or atmosphere)
❖ Water flows from higher (less negative) potential to lower (more negative) potential
❖ Matric potential: Reduction in free energy of water due to attraction of water to soil
matrix- always NEGATIVE- greatest effect on release of water from soil to plants
❖ Total water potential (Pt) Gravitational potential + Matric potential + Osmotic
potential or solute potential + Pressure potential.
❖ At saturated condition pressure potential = osmotic potential
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SAC 101
❖ Soil water potential expressed in Negative sign. Soil water tension / suction expressed
in Positive sign
❖ Saturation water content: all soil pores filled with water; matric potential zero
❖ Field Capacity: Amount of water held by soil at this stage; only micropores are filled
with water & plants absorb water; held at potential of (- 1/3 or – 15 bar)
❖ Permanent wilting coefficient- water is so firmly held - soil particles that plant roots are
unable to draw it; held at tension of 15 bar
❖ Maximum water holding capacity: both micro and macro capillary - completely filled
with water
❖ Sticky point moisture: moisture content of soil at which it no longer sticks to foreign
object- represents maximum moisture content at which a soil remains friable
❖ The percentage of water which soil can retain against centrifugal force of 1000 times that
of gravity- Moisture equivalent
❖ Soil Water Movement: Saturated flow, Unsaturated flow & Water Vapour Movement
❖ Saturated flow occurs when soil pores are completely filled with water. This water moves
at water potentials > – 33 kPa. (flow governed by gravity)
❖ The ease with which soil pores permit water movement ( Permeability)
❖ Hydraulic conductivity- ease with which soil conducts water through its pores
❖ The vertical water flow rate through saturated soil is given by Darcy’s law
❖ Unsaturated flow occurs along soil surfaces, not through large pores. driven by matric
forces- held at water potential of < -1/3 bars
❖ Hysterisis : The moisture content at different tensions during wetting of soil varies from
moisture content at same tensions during drying
❖ Infiltration - downward entry or movement of water into soil surface – vegetative cover
increases infiltration rate
❖ Percolation- The movement of water through column of soil- Sandy soils have greater
percolation than clayey soil
❖ Drainage: It is natural or artificial removal of surface and sub-surface water from given
area
❖ Heat capacity/ thermal capacity: quantity of heat required to raise temperature of unit
mass or volume of body by 1 ˚C expressed as cal/ ˚C
❖ Specific heat: quantity of heat required to raise temperature of 1 g of substance by 1 ˚C or
it is heat capacity / unit mass of substance expressed as cal/g/ ˚C or J/g/ ˚C- on volume
basis- volumetric specific heat cal/ cm3/˚C
❖ Specific heat of soil: 0.2 cal/g; water: 1.0 cal/g; organic matter: 0.5 cal/g
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SAC 101
❖ Thermal conductivity: quantity of heat transmitted through unit of substance per unit
cross-section area per unit temperature gradient per unit time. cal/sec/cm/ ˚C
❖ Order of thermal conductivity sandy> loam> clay > peat
❖ Thermal conductivity increases with increase in wetness, compaction; decreases with
decrease in organic matter
❖ Thermal diffusivity: Thermal conductivity / volumetric heat capacity. cm2/s
❖ Mode of transmission of heat flow in soil through Conduction
❖ Heat flow in soil through conduction is described by Fourier’s law
❖ Light textured sandy soils absorb heat very rapidly than heavy textured soils
❖ Soil aeration facilitates exchange of gases between soil and atmosphere
❖ Composition of soil air oxygen (20.6 %) - atmosphere air (20.79 %); carbondioxide in
soil air (0.03 %) - atmosphere air (0.25 %)
❖ Concentration of CO2 in soil air is 10 times higher than atmospheric air
❖ Soil macro pores are high – Rapid exchange of gases - good soil aeration
❖ Soils on which crops are grown contain more CO2 and less O2 than fallow lands
❖ TILLAGE- exchange of gases faster; puddling decreases macropores and results in
poor aeration
❖ Decomposition of organic matter decrease O2 & increases CO2
❖ Oxygen content of soil air is higher in dry season than during monsoon
❖ Mass Flow- Causes movement of entire mass of air from region of higher pressure to
region of lower pressure – due to total pressure gradient of gases
❖ Diffusion - predominant process of soil aeration- molecular transfer of gases (own
partial pressure)
❖ The diffusive flow of a gas within a porous medium is described by Fick's law.
❖ Oxidized state- N2 & SO4- easily utilized by plants ; Reduced forms - elements – toxic
(Fe2+, Mn2+); Reduced soils have grey & blue colors
❖ Oxygen Diffusion Rate (ODR)- critical value 20 x 10-8 g cm -2 min -1
❖ Redox potential (Eh)- Indicate oxidation and reduction states of soil system
❖ Positive Eh value -oxidized state; Negative Eh value - reduced state
❖ Poor aeration results in ferrous oxide, H2S gas, CO2 gas, ethylene, organic acids, etc., in
soil which is toxic to plants
❖ Soil temperature measurement- Contact type: Bimetallic strip thermometer, Mercury or
Alcohol thermometer and Constant pressure or constant volume thermometer
❖ Soil temperature: Based on electric properties- Thermistors, Thermocouple thermometers
❖ Soil pH is defined as the negative logarithm of hydrogen ion concentration (activity)
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❖ The scale of acidity or alkalinity is called pH scale. This scale ranges from 0 to 14. The
neutral point in this scale is at pH 7
❖ All values > pH 7 represent alkalinity (excess OH- ion) and < 7 denote acidity (excess H+)
❖ The Soil reaction (pH) of solution represents degree of acidity or basicity
❖ Acids soils – Base unsaturated- common in regions of high rainfall- exchange complex
will be dominated by H + ions
❖ Pools of soil acidity: Active acidity, Exchangeable/ Potential/ Salt replaceable/ Reserve
acidity, Residual acidity
❖ Active acidity is a measure of H+ and Al3+ ion activity in soil solution- Magnitude of
acidity is limited
❖ Exchangeable Acidity due to adsorbed H+ & Al3+ on soil colloids
❖ Residual acidity- H & Al atoms bound in non-exchangeable forms- organic matter &
silicate clay
❖ Exchangeable acidity is generally highest for Smectites, intermediate for Vermiculites,
and lowest for Kaolinite- Magnitude of this acidity is very high
❖ Residual acidity is that which remains in soil after active and exchange acidity have been
neutralized
❖ Total acidity= Active acidity + Exchangeable acidity + Residual acidity
❖ Soil pH measures only Active acidity
❖ Alkaline soils - high degree of base saturation
❖ In highly acid soils, availability of nutrients Al, Fe, Mn etc., increased to toxicity level.
The availability of Ca, N, P etc., become unavailable
❖ Most microorganisms function best - pH range 6.0 to 7.5
❖ Phosphorus availability- highest – soil reaction is 6.5 to 7.5
❖ Availability of Potassium (K) - not influenced by soil reaction
❖ When pH is low, solubility of Fe, Al & Mn compounds is increased & are readily
available in acid soils
❖ Availability of B, Cu& Zn reduced in alkaline soils and that of Mo in acid soils.
❖ Availability of Mo- It is more available in neutral and alkaline soils
❖ Neutral to slightly alkaline (6.5 to 8.0) conditions favors bacterial growth
❖ An acid pH (4.5 to 6.5) favors fungal growth, actinomycetes prefer slightly alkaline
❖ % base saturation <80 indicates soil acidity; 80 to 90 - neutral; > 90 - alkaline
❖ Cultural operations in general tend to increase soil acidity
❖ Soils developed from parent material of basic rocks (Basalt) generally have higher pH
than those formed from acid rocks (granite)
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❖ The overall effect of submergence results in increase in pH of acid soil & decrease in pH
of alkaline soil
❖ Buffering refers to resistance to a change in pH
❖ Clay soils rich in organic matter - highly buffered than sandy soils
❖ Greater CEC greater will be the buffer capacity
❖ BUFFER is weak acid and its salt
❖ Soil Electrical Conductivity (EC), is ability of soil to conduct electrical current-
expressed in milli Simens per meter (mS/m) or desi Simen per meter (dS/m)
❖ EC measures- Soil salinity -measure of total amount of soluble salts (chlorides, sulphates
and nitrates of Ca, Mg, Na) in soil.
❖ The colloidal state refers to a two-phase system in which one material in a very finely
divided state is dispersed through second phase.
❖ Size of soil colloids <0.001 mm
❖ Inorganic colloids: Silicate clays (Layer Silicate Clays & Amorphous Clays (non-
crystalline)), Iron and Al hydroxide clays
❖ Organic Colloids- Humus
❖ Surface area is area of clay particle that is accessible to ions/molecules
❖ Small size of soil colloids- larger external surface area per unit mass
❖ All clays particles- expose large external surface
❖ External surface area of Kaolinite- 30-35 m2/g
❖ Internal surface area of Montmorillonite- 500-600 m2/g; Vermiculite- 700-800 m2/g
❖ Most of organic and inorganic soil colloids carry a negative charge
❖ Due to cohesive force- clay particle are able to form aggregates
❖ Smectite group like Montmorillonite swell when wet and shrink when dry
❖ Soils dominated by kaolinite, chlorite, or fine grained micas do not swell or shrink-
Vermiculite is intermediate
❖ The phenomenon of coalescence and formation of flocks is known as flocculation (Ca &
Mg)
❖ The reverse process of breaking up of flocks into individual particles is de-flocculation
or dispersion (Na)
❖ Colloids are unable to pass through a semi permeable membrane
❖ Iron and aluminum oxide clays (Sesquioxide clays): Under conditions of extensive
leaching by rainfall (warm humid climate)- clays do not swell, not sticky and have high
phosphorus adsorption capacity
❖ Sesquioxides (mixture of oxides and hydroxides of iron and aluminum)
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❖ Sources of negative charge on clays: Isomorphous substitution, Ionizable hydrogen ions
& Anion exchange
❖ Isomorphous substitution / Permanent / pH independent charges/ Constant surface
charges : cation of higher valence with another cation of lower valence but of similar size
in clay crystal structure may occur; Si4+ replaced by A13+, and replacement of A13+ by
Fe3+, Fe2+, Mg2+ or Zn2+. 2:1 type clay minerals, 2:2 type clay minerals
❖ Ionizable hydrogen ions / Exposed crystal edges/ pH dependent charges / variable
charges: The Al-OH or -Si-OH portion of clay ionizes H and leaves an un-neutralized
negative charge on oxygen (-AlO- or - SiO-). Especially Kaolinite & Humus
❖ The Ion Exchange phenomenon was first identified by Harry Stephen Thompson (1850)
❖ Cation exchange phenomenon was first discovered by Thomas Way (1850)
❖ Common exchangeable cations are Ca2+, Mg2+, H+, K+, NH + and Na+
❖ The common anions are SO4 2-, Cl -, PO4 3- and NO3 -
❖ The unit of CEC is Cmol (p+) / kg ; AEC is Cmol (e-) / kg or milliequivalent / 100 g
❖ Principles governing cation exchange reactions: Reversibility, Charge Equivalence,
Fixed ratio law, complementary ion effect
❖ Replacing power of ions increases with atomic weight
❖ H+ ions are adsorbed more strongly than other monovalent or divalent ions.
❖ The replacing power of cation: H+ > Al3+ > Ca2+> Mg2+ > K+ = NH+4 > Na+
❖ CEC (Cmol (p+)/ Kg) of Vermiculite- 100-150, Montmorillonite- 80- 100, Illite- 15-40,
Chlorite- 10-40, Kaolinite- 3- 15
❖ Out of all exchangeable bases, Ca2+ is dominant cation
❖ % Base saturation = Exchangeable base forming cation / CEC x 100
❖ Base Saturation Percentage > 80 % – highly fertile soil; 50-80 %- medium fertile soil;
<50 %- less fertile soil
❖ Higher the pH, higher CEC; Lower pH, greater AEC
❖ Soils with Kaolinite dominant clay have higher AEC than 2:1 type clay
❖ The relative order of anion exchange is OH- > H2 PO4- > SO42- > NO3- > Cl –
❖ The phenomenon of anion exchange is important release of fixed P in soil
❖ Soil Organic Matter is generally used to represent organic constituents in soil, including
undecayed plant and animal tissues, their partial decomposition products, and soil
biomass
❖ Soil Organic Matter: Natural C-containing organic materials living or dead
❖ Sources of Soil Organic Matter: Primary sources- Plant tissues; Secondary sources-
Animals waste products
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❖ Dominant organic compounds in plants residues is Carbohydrates (60 %), Lignins (10 –
30 %), Fats, waxes, tannin (1– 8 %), Proteins (1 – 5 %)
❖ Sugars, starches, proteins - Rapidly decomposed; Hemicelluloses, celluloses - Less
rapidly decomposed; Fats, waxes, resins, lignins- Very slowly decomposed
❖ Simple decomposition products- aerobic decomposition are CO2, H2O, NO -3, SO 4 2-
❖ Products formed- anaerobic conditions CH4, NH4 2-, organic acids like lactic, propionic,
butyric, H2S etc
❖ Ammonification is process of transformation of organic nitrogenous compounds into
ammonia- by heterotrophic microbes- aerobic process
❖ Nitrification is process of conversion of ammonia to nitrites (NO2-) and then to nitrate
(NO3 -) – ammonia is converted to nitrite by Nitrosomonas & nitrite to nitrate by
Nitrobacter- aerobic process by autotrophic bacteria
❖ Denitrification- The process, of conversion of nitrate into gaseous nitrogen (N2) or
nitrous oxide (N2O) by Pseudomonas / Bacillus- water logging and high pH favours
❖ Aminization: The process of conversion of proteins to aminoacids
❖ Breakdown of Cellulose to cellobiose by cellulase; Cellobiose to glucose by cellobiase
❖ Breakdown of Hemicellulose to sugars and uronic acid by hemicellulase
❖ Enzyme involved in breakdown of lignin is lignase/ligninase
❖ Enzyme involved in sulphur oxidation – sulphatase by Thiobacillus; mineralization of
phosphorus by enzyme phosphatase
❖ Carbon:Nitrogen (C : N) ratio- intimate relationship- organic matter (C) & nitrogen
contents of soil
❖ Wider C:N ratio leads to slow decomposition rate
❖ Narrow C:N ratio, plant residues decompose quickly and release nutrients readily
❖ C:N humus- 10:1; microbes- 4:1 to 9:1; arable soils – 5:1 to 15:1
❖ Organic matter maintains favourable condition of aeration and permeability in soil;
Water holding capacity of soil is increased
❖ Surface mulching with organic matter lowers wind erosion and lowers soil temperatures
in summer and keeps soil warmer in winter
❖ Litter: It comprises the dead plant and animal debris on the soil surface
❖ Organic matter serves as source of energy for microbes, as a reservoir of nutrients for
plant growth
❖ Organic acids released from decomposing organic matter help to reduce alkalinity in
soils
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❖ Humus (final product of decomposition of OM) provides storehouse of nutrients- acts
as buffering agent
❖ OM influence soil colour - adequate amount – brown to dark brown or black
❖ OM acts as a chelate binding – soluble chelates- increasing availability of micronutrients
for plant uptake
❖ Humus is a complex and rather resistant mixture of brown or dark brown amorphous
and colloidal organic substance that results from microbial decomposition and synthesis-
relatively stable
❖ Soil organic matter fractions: Humic matter & Non- humic matter
❖ Humic group 60-80% of soil organic matter- most complex- resistant to microbial
attack- aromatic ring structure- polyphenols and poly quinones
❖ Humic group consists of series of substances such as Fulvi acid, Humic acid & Humin
❖ Fulvic acid (FA): Light yellow coloured, lowest molecular weight, more aliphatic and is
alkali and acid soluble
❖ Humic acid (HA): Dark brown to black coloured, medium molecular weight, aromatic,
alkali-soluble and acid-insoluble
❖ Humin (HN): Humin is very stable, highest molecular weight and is insoluble in both
alkali and acid
❖ Non humic group: 20-30% of organic matter in soil- less complex and less resistant to
microbial attack than humic- polysaccharides like carbohydrates, sugars, proteins, etc
❖ Theories on humus formation: Lignin theory: Proposed by Waksman (1932);
Kononovas’ theory; Polyphenol theory: (Flaig and Sochtig, 1964)
❖ Lignin theory- humic substances are formed due to incomplete degradation of lignin
❖ Kononovas’ theory: humic substances are formed by cellulose decomposing
mycobacteria- Polyphenols oxidized to quinones – react with N compounds
❖ Polyphenol theory: humic substances are formed by condensation of phenolic
materials- quinones are condensed with low molecular weight microbial products
❖ Humus: negatively charged; very high surface area, higher CEC (150 – 300 cmol/kg), 4 -
5 times higher WHC than that of silicate clays- Impart black color to soils
❖ Various clay minerals can bind humus substances through some linkages known as clay-
humus complex
❖ Humic acid is arranged on external surface of clay- easily extracted by alkali- Unstable
❖ Interaction of clay, humic acid and exchangeable cations (Fe, Al, Ca, Mg) occurring in
lattice of clay mineral this humic acid is not extracted by alkali- Stable
❖ Soil flora and Soil fauna are terms used to describe organisms that live within soils
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❖ The flora is composed primarily of microorganisms such as bacteria, actinomycetes,
algae and fungi
❖ The fauna is composed of microfauna such as protozoans, mesofauna such as nematodes
and mites, centipedes, springtails,and macrofauna such as insects and worms
❖ Microfauna and Microflora: 1-100 μm; Mesofauna: 100 μm -2 mm; Macrofauna: 2-20
mm; Megafauna: > 20 mm
❖ Bacteria are most abundant group of micro-organism in soil in number
❖ Autotropic nitrifying bacteria- Nitrosomonas, nitrobacter; Sulphur oxidizing bacteria-
Thiobacillus; Denitrifying bacteria- Psedumonas, Bacillus; Ferrobacillus – Converts
ferrous to ferric
❖ Symbiotic, non-symbiotic and cellulose decomposers come under Heterotrophs
❖ Nitrifiers, denitrifiers, Nitrate formers and sulphur oxidizers are autotrophs
❖ Actinomycetes presence is responsible for "earthy" aroma (Geosmin) which is associated
with good healthy soil
❖ Fungi live in symbiotic association with roots of higher plants- “mycorrhizal
association”- increases availability of several essential nutrients
❖ Fungi is dominant microbe in biomass compared to bacteria
❖ Soil enzymes: Urease (helps in breakdown of urea), Protease, Cellulase (breaks
cellulose), Hemicellulase(Hemicellulose), Ligninase/ Lignase (degrades Lignin),
Phosphatase, Sulphatase.
❖ Biomass carbon: part of carbon assimilated by microorganisms and incorporated into
microbial tissue
❖ Biomass nitrogen: as part of nitrogen assimilated by microorganisms and incorporated
into microbial tissue
❖ Carbon sequestration is process of transforming carbon in air (CO2) into stored soil
organic carbon (storage of carbon in stable solid form)
❖ Carbon trading is market-based system aimed at reducing greenhouse gases that
contribute to global warming, particularly carbon dioxide
❖ Carbon trading: Carbon CAP- Trade program & Carbon offsetting
❖ Carbon CAP- Trade program: Assignment of an upper threshold limit on amount of
pollutant that can be emitted by country; TRADE- excess or unused allowances/ credits
can be traded to the countries whose emissions have exceeded their assigned cap
❖ Carbon trading emission mechanisms: Emission Trading (ET), Clean Development
Mechanism (CDM), Joint Implementation (JI)
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❖ Emission Trading (ET): Countries whose emissions are less than their assigned amount
can sell the excess amount to countries whose emissions have exceeded their assigned
amount
❖ Clean Development Mechanism (CDM): Developed countries can fund emission
reduction projects in developing nations whose emissions have exceeded their assigned
amount
❖ Joint Implementation (JI): Developed countries can implement emission reduction
projects in another developed country with common idea on reduction of carbon
emission
❖ Kyoto protocol: Adopted on 11 Dec 1997, Came to force on 16 Feb 2005- Aims to
reduce emissions of green house gases
❖ Avoiding emissions by maintaining existing carbon storage in trees and soils
❖ Increasing carbon storage by, e.g., tree planting, conversion from conventional to
conservation tillage practices on agricultural lands; Increased crop rotation intensity;
Using higher residue crops; cover crops
❖ Soil pollution is defined as contamination of soil of a particular region due to excess
application of chemicals in form of fertilizers, pesticides, etc
❖ Excess amount of fertilizers in soils makes the soil either acidic or alkaline and pollutes
it
❖ Excess fertilizers discharge to water bodies increase algal growth on surface water-
Eutrophication (on increase amounts of Phosphorus & nitrate nitrogen)
❖ Inorganic contaminants: Trace elements concentrated in irregular way- usually metals-
heavy metals (density > 6 g/cc)- Some are essential, but all are toxic to organisms at
higher concentrations
❖ Cd (cadmium) and Arsenic (As)- extremely poisonous; Mercury, lead & Ni- moderately
poisonous; Cu, Zn & Mn – relatively lower toxicity- phytotoxic effect, higher level of
heavy metals-disturb nutrient balance in soil- affect biochemical processes & crop yields
❖ On accumulation pesticides in soil- increase in concentration of chemicals upto food
chain- This increase in concentration up to food chain – biological magnification
❖ Effect of soil pollution: reduced soil fertility, reduced availability of nutrients, reduced
crop yield, imbalance of soil flora and fauna
❖ Methods to control soil pollution: Integrated Crop Management, intercropping, crop
rotation, green manuring, Less use of chemical fertilizers & pesticides, Integrated
nutrient management (INM)- Combine use of chemical-organic- biofertilizers, Soil
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organic matter, Integrated pest management (IPM), Integrated weed management
(IWM), Bioremediation, Phytoremediation
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