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Principles of terrestrial ecosystem ecology.pdf

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66 3. Geology and Soils<br />

ferent cations are held to the exchange<br />

complex. In general, cations occupy exchange<br />

sites and displace other ions in the sequence<br />

H(Al 3+ ) > H + > Ca 2+ > Mg 2+ > K +<br />

ª NH4 + > Na + (3.4)<br />

so leached soils tend to lose Na + and NH4 + but<br />

retain Al 3+ and H + . This displacement series is a<br />

consequence <strong>of</strong> differences among ions in<br />

charge and hydrated radius. Ions with more<br />

positive charges bind more tightly to the<br />

exchange complex than do ions with a single<br />

charge. Ions with a smaller hydrated radius<br />

have their charge concentrated in a smaller<br />

volume and tend to bind tightly to the exchange<br />

complex.<br />

Minerals like the iron and aluminum oxides<br />

found in many tropical soils have surface<br />

charges that vary between positive and negative,<br />

depending on pH. At the low pH conditions<br />

typical <strong>of</strong> these soils, the net charge is<br />

sometimes positive (Uehara and Gillman<br />

1981), so they attract anions, creating an anion<br />

exchange capacity. As with cations, anion<br />

absorption depends on the concentration <strong>of</strong><br />

anions and their relative capacities to be held<br />

or to displace other anions. Anions generally<br />

occupy exchange sites and displace other ions<br />

in the sequence<br />

PO4 3- > SO4 3- > Cl - > NO3 - (3.5)<br />

so leached soils tend to lose NO3 - and Cl - but<br />

retain phosphate (PO4 3- ) and sulfate (SO4 3- ).<br />

This retention reflects both anion exchange and<br />

the formation <strong>of</strong> covalent bonds that are not<br />

readily broken.<br />

The high CEC and base saturation found in<br />

many soils, especially in many temperate soils,<br />

provide buffering capacity that keeps the soils<br />

from becoming acid. When additional H + is<br />

added to the system in solution (e.g., in acid<br />

rain), it exchanges with cations that were held<br />

on cation exchange sites on clay minerals and<br />

soil organic matter. Buffering capacity allows<br />

the pH in forest soils to remain relatively<br />

constant for long periods despite chronic exposure<br />

to acid rain. When the buffering capacity<br />

is exceeded, the soil pH begins to drop, which<br />

can solubilize aluminum hydroxides (Al(OH)x),<br />

Al 3+ , and other cations, with potentially toxic<br />

effects on both <strong>terrestrial</strong> and downstream<br />

aquatic <strong>ecosystem</strong>s (Schulze 1989, Aber et al.<br />

1998). In many tropical soils, the relatively low<br />

CEC does not function as efficiently to buffer<br />

soil solution chemistry. Additions <strong>of</strong> acids to<br />

these already acidic unbuffered systems<br />

releases aluminum in solution more readily,<br />

making these soils potentially toxic to many<br />

plants and microbes.<br />

Summary<br />

Five state factors control the formation and<br />

characteristics <strong>of</strong> soils. Parent material is generated<br />

by the rock cycle, in which rocks are<br />

formed, uplifted, and weathered to produce the<br />

materials from which soil is derived. Climate is<br />

the factor that most strongly determines the<br />

rates <strong>of</strong> soil-forming processes and therefore<br />

rates <strong>of</strong> soil development. Topography modifies<br />

these rates at a local scale through its effects on<br />

microclimate and the balance between soil<br />

development and erosion. Organisms also<br />

strongly influence soil development through<br />

their effects on the physical and chemical environment.<br />

Time integrates the impact <strong>of</strong> all state<br />

factors in determining the long-term trajectory<br />

<strong>of</strong> soil development. In recent decades, human<br />

activities have modified the relative importance<br />

<strong>of</strong> these state factors and substantially altered<br />

Earth’s soils.<br />

The development <strong>of</strong> soil pr<strong>of</strong>iles represents<br />

the balance between pr<strong>of</strong>ile development, soil<br />

mixing, erosion, and deposition. Pr<strong>of</strong>ile development<br />

occurs through the input, transformation,<br />

vertical transfer, and loss <strong>of</strong> materials from<br />

soils. Inputs to soils come from both outside the<br />

<strong>ecosystem</strong> (e.g., dust or precipitation inputs)<br />

and inside the <strong>ecosystem</strong> (e.g., litter inputs).<br />

The organic matter inputs are decomposed to<br />

produce CO2 and nutrients or are transformed<br />

into recalcitrant organic compounds. The carbonic<br />

acid derived from CO2 and the organic<br />

acids produced during decomposition convert<br />

primary minerals into clay-size secondary<br />

minerals, which have greater surface area and<br />

cation exchange capacity. Water moves these<br />

secondary minerals and the soluble weathering<br />

products down through the soil pr<strong>of</strong>ile until

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