Environmental Geosciences II: Weathering, Erosion, Transport and Deposition, Soil Formation, Clay Minerals, Soil Physical and Chemical Properties, Soil Types and Cation Exchange Capacity, the Geochemical Classification and Abundance of Elements, Partitioning and Recycling, and Palaeoclimate

This chapter takes Unit IV's second and third items: the surface processes that break rocks down and make soils, and the geochemistry that governs where elements go. It covers physical, chemical and biological weathering, with the key reactions; erosion, transport and deposition of sediment; soil-forming minerals and the processes and factors of soil formation, with the climatic control; the identification and characterisation of clay minerals; the physical and chemical properties of soils, with porosity and cation exchange capacity worked; the soil types of India; Goldschmidt's geochemical classification and the abundance of elements in the bulk Earth, crust, hydrosphere and biosphere; the partitioning and recycling of elements in surface processes; and the reconstruction of palaeoclimate. The chemistry of soil organic matter and nutrient cycles was taught in Unit II.

1. Weathering, erosion, transportation and deposition

Weathering is the breakdown of rocks in place at or near the surface. Physical weathering breaks rock without changing its composition: frost wedging as water expands by about 9% on freezing, salt crystallisation in arid and coastal areas, thermal expansion and contraction, and exfoliation as overburden is removed and rock expands. Chemical weathering changes the minerals themselves, and it is fastest where it is warm and wet. Biological weathering includes the prying of roots and the acids secreted by lichens and microbes. The resistance of minerals to chemical weathering follows the Goldich stability series, the reverse of Bowen's crystallisation order: olivine and calcium plagioclase weather fastest and quartz is the most resistant, which is why quartz sand is the common residue of weathering.

Chemical weathering reactionExampleProduct
Hydrolysis2KAlSi₃O₈ + 2H⁺ + 9H₂O → Al₂Si₂O₅(OH)₄ + 4H₄SiO₄ + 2K⁺ (feldspar → kaolinite)Potassium feldspar weathers to kaolinite clay, releasing potassium and dissolved silica
Carbonation and dissolutionCaCO₃ + CO₂ + H₂O → Ca²⁺ + 2HCO₃⁻Limestone dissolves, forming karst landscapes and caves; this reaction removes atmospheric CO₂ over geological time
OxidationFe²⁺ in olivine, pyroxene and biotite oxidised to Fe³⁺Red and yellow iron oxides and hydroxides (haematite, goethite) that colour tropical soils
Hydration and chelationAnhydrite + water → gypsum; organic acids binding metal ionsExpansion of minerals; mobilisation of iron and aluminium in acid soils

Erosion removes the weathered material, by running water, wind, glaciers, waves and mass movement on slopes, and transport carries it: in solution, in suspension (fine silt and clay), by saltation (bouncing sand grains) and by traction (rolling and sliding of the coarsest). Hjulström's curve relates stream velocity to erosion, transport and deposition: fine sand of about 0.1 to 0.5 mm is eroded at the lowest velocity; coarser grains need more velocity because they are heavier; and silt and clay, though fine, also need higher velocity to erode because they are cohesive, yet once suspended they settle only in almost still water. Deposition therefore sorts sediment, gravel in channels, sand on bars and silt and clay on floodplains, in lakes and in the sea.

2. Soil-forming minerals, the process of soil formation and the climatic control, and the soil types of India

Hans Jenny (1941) expressed soil as a function of five state factors, s = f(cl, o, r, p, t): climate, organisms, relief, parent material and time, the "clorpt" equation. Climate is the most important over large areas, because temperature and rainfall set the rates of weathering, leaching and organic-matter turnover. Soils develop horizons: an O horizon of organic litter, an A horizon of mixed humus and mineral matter, an E horizon from which clay, iron and aluminium are leached (eluviated), a B horizon where they accumulate (illuviated), a C horizon of weathered parent material and the R layer of bedrock.

Soil-forming processClimateResult
PodzolisationCool, humid, under conifersAcid leaching of iron, aluminium and humus from a bleached E horizon into the B horizon; podzols (spodosols)
LaterisationHot, humid tropics with alternating wet and dry seasonsIntense leaching removes silica and bases, leaving residual iron and aluminium oxides; laterites, and bauxite where aluminium is enriched
CalcificationSemi-arid grasslandsLimited leaching; calcium carbonate accumulates in the B or C horizon; fertile chernozems (mollisols)
Salinisation and alkalisationArid and semi-arid, or poorly drained irrigated landEvaporation concentrates soluble salts at the surface (saline soils); exchangeable sodium makes sodic (alkali) soils
GleisationWaterloggedReducing conditions give grey and bluish colours with rust-coloured mottles; gley soils

The Indian Council of Agricultural Research recognises eight major soil groups: alluvial soils of the Indo-Gangetic plain and deltas, the most extensive and agriculturally important; black soils (regur) formed from the Deccan basalts, rich in smectite, highly retentive of moisture, swelling when wet and cracking deeply when dry, and suited to cotton; red soils on the crystalline rocks of the peninsula, coloured by ferric oxides; laterite soils of the high-rainfall Western Ghats, Odisha and the north-east; arid (desert) soils of Rajasthan; forest and mountain soils; saline and alkaline soils; and peaty and marshy soils of Kerala's kari lands and the coastal wetlands.

3. Clay minerals, soil physical and chemical properties and cation exchange capacity

Clay minerals are layer silicates built of sheets of silica tetrahedra (T) and aluminium or magnesium octahedra (O). Isomorphous substitution, such as Al³⁺ for Si⁴⁺ in the tetrahedral sheet or Mg²⁺ for Al³⁺ in the octahedral sheet, leaves a permanent negative charge that is balanced by exchangeable cations. They are identified chiefly by X-ray diffraction, from the basal spacing between layers and how it changes when the sample is saturated with glycol or heated, supported by differential thermal analysis, infrared spectroscopy and electron microscopy.

Clay mineralStructure and basal spacingCEC (cmol(+)/kg) and behaviour
Kaolinite1:1 (T-O), layers held by hydrogen bonds; about 0.7 nm, non-expandingAbout 3 to 15; low plasticity; dominant in highly weathered tropical soils
Illite2:1 (T-O-T) with potassium locking the layers; about 1.0 nm, non-expandingAbout 10 to 40; common in temperate soils and sediments
Smectite (montmorillonite)2:1 with weakly held hydrated cations; about 1.4 nm, expanding to about 1.7 nm with glycolAbout 80 to 150; shrinks and swells; dominant in black cotton soils
Vermiculite and chloriteVermiculite 2:1, limited expansion; chlorite 2:1:1 with a hydroxide interlayer, about 1.4 nm, non-expandingVermiculite about 100 to 150; chlorite about 10 to 40

The physical properties of soil begin with texture, the proportions of sand (2 to 0.05 mm on the USDA scale), silt (0.05 to 0.002 mm) and clay (below 0.002 mm), read from the textural triangle, and structure, the arrangement of particles into aggregates. Bulk density is the dry mass per unit of total volume, usually 1.1 to 1.6 g/cm³, rising with compaction; particle density, the density of the solids alone, is close to 2.65 g/cm³ for most mineral soils; and porosity = 1 − (bulk density ÷ particle density), so a soil of bulk density 1.325 g/cm³ has a porosity of 1 − 0.5 = 50%. Water is held between field capacity, after free drainage, and the permanent wilting point, and the difference is the water available to plants, greatest in loams.

The chemical properties are pH, electrical conductivity (a measure of soluble salts), organic carbon and, above all, the cation exchange capacity: the total quantity of exchangeable cations a soil can hold, expressed in centimoles of positive charge per kilogram (numerically equal to milliequivalents per 100 g). CEC comes from the permanent charge of clays and the pH-dependent charge of humus and oxides, so it is controlled by mineralogy and organic matter. Humus has the highest CEC, around 200 cmol(+)/kg or more, smectite around 100 and kaolinite around 10. A soil with 30% smectite, 10% kaolinite and 2% humus therefore has a CEC of about 0.30 × 100 + 0.10 × 10 + 0.02 × 200 = 30 + 1 + 4 = 35 cmol(+)/kg. Base saturation is the percentage of the CEC occupied by the basic cations Ca²⁺, Mg²⁺, K⁺ and Na⁺, falling as soils acidify. CEC governs fertility, the retention of heavy metals and pesticides, and a soil's capacity to buffer acid rain.

🎯 Why black soils crack and laterites do not
The difference is clay mineralogy. Smectite takes water between its layers and swells, then shrinks on drying, so black cotton soils crack deeply in the dry season and are difficult foundations for roads and buildings. The kaolinite and oxides of laterites do not expand, so these soils stay firm, are low in CEC and fertility, and harden irreversibly on exposure, which is why laterite was quarried as a building stone.

4. The geochemical classification and abundance of elements, partitioning and recycling

Goldschmidt classAffinityExamplesWhere concentrated
SiderophileIron-loving; alloy with metallic ironFe, Ni, Co, Au, Pt, IrThe core, which is why platinum-group metals are scarce in the crust
ChalcophileSulphur-loving; form sulphidesCu, Zn, Pb, Hg, Ag, Cd, AsSulphide ore deposits, which on weathering release metals and acid mine drainage
LithophileOxygen-loving; form silicates and oxidesSi, Al, Na, K, Ca, Mg, the rare earths, U, ThThe crust and mantle
AtmophileVolatile, gaseousN, the noble gases, HThe atmosphere and hydrosphere

Abundances differ sharply between reservoirs. By mass the bulk Earth is dominated by iron (about 32%), oxygen (about 30%), silicon (about 15%) and magnesium (about 14%), iron being so abundant because of the core. The crust, by contrast, is led by oxygen, silicon and aluminium. Sea water, apart from hydrogen and oxygen, is dominated by chloride (about 19.4 g/kg) and sodium (about 10.8 g/kg), followed by sulphate, magnesium, calcium and potassium, for a total salinity of about 35 g/kg. The biosphere is built mainly of the light elements: the human body is about 65% oxygen, 18% carbon, 10% hydrogen and 3% nitrogen by mass, with calcium and phosphorus next.

How an element is partitioned during weathering and sedimentation depends largely on its ionic potential, the ratio of its charge to its ionic radius. Ions of low ionic potential, such as Na⁺, K⁺, Ca²⁺ and Mg²⁺, stay in solution as cations and are carried to the sea; those of intermediate ionic potential, such as Al³⁺, Fe³⁺ and Ti⁴⁺, hydrolyse and precipitate as insoluble hydroxides (the hydrolysates) and stay behind in soils and laterites; and those of high ionic potential, such as C, N, S and P, form soluble oxyanions such as carbonate, nitrate, sulphate and phosphate. Redox conditions add a second control, iron and manganese being mobile when reduced and immobile when oxidised. Elements are recycled geochemically by the rock cycle: weathering releases them, rivers carry them to the ocean, sedimentation and burial lock them into rock, and subduction, metamorphism and volcanism return them to the surface over tens to hundreds of millions of years.

5. Palaeoclimate

Palaeoclimate is reconstructed from proxies, natural archives that record past conditions. Ice cores preserve both the isotopic composition of the snow, whose δ¹⁸O and δD become more negative in colder periods, and bubbles of ancient air, giving past carbon dioxide and methane directly; the EPICA Dome C core from Antarctica extends about 800,000 years and shows carbon dioxide varying between roughly 180 ppm in glacial periods and 280 ppm in interglacials, far below today's levels. In marine sediments the δ¹⁸O of foraminiferal shells rises when the climate is cold and ice sheets lock up light ¹⁶O. Tree rings, corals, pollen in lake and bog sediments, cave speleothems and annually layered lake varves fill in finer detail.

Over the last few million years the glacial-interglacial cycles have been paced by the Milankovitch cycles, periodic changes in the Earth's orbit that redistribute sunlight by season and latitude: eccentricity, the shape of the orbit, with periods of about 100,000 and 400,000 years; obliquity, the tilt of the axis between about 22.1° and 24.5°, with a period of about 41,000 years; and precession, the wobble of the axis, with periods of about 19,000 to 23,000 years. The orbital changes are small, and feedbacks from greenhouse gases and ice albedo amplify them. The Last Glacial Maximum was about 21,000 years ago, when sea level was more than 100 m lower, and the present interglacial, the Holocene, began about 11,700 years ago. The palaeoclimate record matters because it shows how sensitive the climate is to carbon dioxide and how fast it has changed before.

Key takeaways

  • Chemical weathering (hydrolysis, carbonation, oxidation) is fastest where it is warm and wet; quartz resists it most; Hjulström's curve shows fine sand is eroded most easily.
  • Soil = f(climate, organisms, relief, parent material, time); podzolisation, laterisation, calcification, salinisation and gleisation follow climate and drainage; India has eight major soil groups from alluvial to peaty.
  • Kaolinite (1:1, 0.7 nm) has low CEC; smectite (2:1, expanding) has high CEC and swells; XRD identifies them; porosity = 1 − BD ÷ PD and CEC sums the contributions of clays and humus.
  • Goldschmidt's classes are siderophile, chalcophile, lithophile and atmophile; the bulk Earth is iron-rich, the crust oxygen- and silicon-rich and sea water chloride- and sodium-rich; ionic potential decides whether an element dissolves, hydrolyses or forms an oxyanion.
  • Ice cores, foraminiferal δ¹⁸O, tree rings and pollen reconstruct palaeoclimate; Milankovitch cycles of about 100,000, 41,000 and 19,000 to 23,000 years pace the ice ages.

Practice questions (10)

Attempt each one before opening the answer. Every explanation names the tempting wrong option as well as the right one, because that is where marks are lost.

  1. Jenny's equation expresses soil as a function of which five factors?

    1. Temperature, rainfall, wind, sunlight and humidity
    2. Climate, organisms, relief, parent material and time
    3. Sand, silt, clay, humus and water
    4. pH, CEC, porosity, texture and colour
    Show answer

    Answer: B — Climate, organisms, relief, parent material and time

    Jenny (1941) wrote s = f(cl, o, r, p, t), the clorpt state factors of soil formation. The other options list soil components, soil properties or elements of climate alone, which is only one of the five factors.
  2. A soil has a bulk density of 1.325 g/cm³ and a particle density of 2.65 g/cm³. What is its porosity in per cent?

    Numerical answer — type the value.

    Show answer

    Answer: 50

    Porosity = 1 − (bulk density ÷ particle density) = 1 − (1.325 ÷ 2.65) = 1 − 0.5 = 0.5, that is 50%. Dividing particle density by bulk density (2.0) or subtracting the densities (1.325) does not give the pore fraction.
  3. Which clay mineral has the highest cation exchange capacity and swells strongly on wetting?

    1. Kaolinite
    2. Quartz
    3. Illite
    4. Smectite (montmorillonite)
    Show answer

    Answer: D — Smectite (montmorillonite)

    Smectite is a 2:1 clay whose layers are held only by hydrated cations, so water enters between them, the lattice expands and a large internal surface carries a high CEC of about 80 to 150 cmol(+)/kg. Kaolinite is 1:1 and non-expanding with low CEC, illite is locked by potassium, and quartz is not a clay mineral.
  4. Which of the following are chalcophile elements in Goldschmidt's classification? Select all that apply.

    1. Potassium
    2. Zinc
    3. Lead
    4. Copper
    Show answer

    Answer: B — Zinc; C — Lead; D — Copper

    Copper, zinc and lead combine readily with sulphur and occur mainly as sulphide ores such as chalcopyrite, sphalerite and galena. Potassium is lithophile, bound in silicates such as feldspar and mica.
  5. Laterisation is the soil-forming process in which

    1. salts accumulate at the surface through evaporation in arid lands
    2. iron and aluminium are leached from a bleached horizon under cool coniferous forest
    3. intense leaching in the hot, humid tropics removes silica and bases, leaving iron and aluminium oxides
    4. calcium carbonate accumulates in the subsoil of semi-arid grasslands
    Show answer

    Answer: C — intense leaching in the hot, humid tropics removes silica and bases, leaving iron and aluminium oxides

    Laterisation desilicates the soil, leaving residual iron and aluminium oxides; where aluminium is enriched, bauxite forms. The other options describe calcification, podzolisation and salinisation respectively.
  6. Assertion (A): Black cotton soils develop deep cracks in the dry season. Reason (R): They are rich in smectite, which swells on wetting and shrinks on drying. Choose the correct option.

    1. Both A and R are true, and R is the correct explanation of A
    2. Both A and R are true, but R is not the correct explanation of A
    3. A is true, but R is false
    4. A is false, but R is true
    Show answer

    Answer: A — Both A and R are true, and R is the correct explanation of A

    Both are true and R explains A. The expanding smectite of the Deccan basalt soils takes water between its layers in the monsoon and loses it in the dry months, and the shrinkage opens deep cracks; this also makes them difficult foundations for roads and buildings.
  7. The Milankovitch cycle associated with changes in the tilt of the Earth's axis (obliquity) has a period of about

    1. 21,000 years
    2. 100,000 years
    3. 41,000 years
    4. 11,700 years
    Show answer

    Answer: C — 41,000 years

    Obliquity varies between about 22.1° and 24.5° over about 41,000 years. About 100,000 years is eccentricity, about 19,000 to 23,000 years is precession, and 11,700 years is the age of the Holocene, not an orbital period.
  8. Which of the following are used as proxies to reconstruct past climate? Select all that apply.

    1. Air bubbles trapped in Antarctic ice cores
    2. The present-day NDVI of a forest
    3. The oxygen-isotope ratio of foraminiferal shells in marine sediments
    4. The Mohs hardness of a mineral
    Show answer

    Answer: A — Air bubbles trapped in Antarctic ice cores; C — The oxygen-isotope ratio of foraminiferal shells in marine sediments

    Ice-core bubbles give past carbon dioxide and methane directly, and foraminiferal δ¹⁸O records past temperature and ice volume. A present-day vegetation index says nothing about the past, and mineral hardness is a physical property with no climatic record in it.
  9. Estimate the cation exchange capacity, in cmol(+)/kg, of a soil containing 30% smectite (CEC 100 cmol(+)/kg), 10% kaolinite (CEC 10 cmol(+)/kg) and 2% humus (CEC 200 cmol(+)/kg), the rest contributing nothing.

    Numerical answer — type the value.

    Show answer

    Answer: 35

    CEC = 0.30 × 100 + 0.10 × 10 + 0.02 × 200 = 30 + 1 + 4 = 35 cmol(+)/kg. Even at only 2% by mass the humus adds four times as much as the kaolinite, which is why organic matter matters so much to a soil's exchange capacity.
  10. The hydrolysis of potassium feldspar during chemical weathering produces

    1. haematite and sulphuric acid
    2. kaolinite clay, dissolved silica and potassium ions
    3. quartz and methane
    4. calcite and carbon dioxide
    Show answer

    Answer: B — kaolinite clay, dissolved silica and potassium ions

    2KAlSi₃O₈ + 2H⁺ + 9H₂O → Al₂Si₂O₅(OH)₄ + 4H₄SiO₄ + 2K⁺: feldspar reacts with acidified water to give kaolinite, silicic acid and potassium, which is how clays and much river-borne potassium and silica originate. Haematite comes from the oxidation of iron-bearing minerals, not from feldspar.