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Special Topics on Soils
- Water Movement in Soils
- Effects of Saturation by Water on Soils
- Fragipans
1. Forces that Control Water Movement
Water movement in soil takes place in response to a force, or potential. The
types of forces that act on water moving through a soil include:
- positive forces, such as gravity and pressure
- negative forces, such as suction and osmosis
These forces, in conjunction with the water content of the soil, dictates
whether the soil water moves through the soil by “saturated” or “unsaturated”
flow.
Saturated flow:
- driving force is positive (gravity or pressure)
- soil water is conducted by all pores
- the rate of flow is greatest through the large connective pores, so
saturated flow is higher in sandy soils
Unsaturated flow:
- driving force is suction
- soil water is conducted only by the smaller pores; large connective
pores are filled with soil air
- soil water tends to only occupy the smaller pores, so unsaturated flow
tends to be higher in clayey soils
2. Soil Physical Properties that Control Water Movement
In addition to the above forces, water movement in some soils is controlled
by the type of soil structure present within the soil horizons. Water moving
downward vertically through a soil profile is transported in the pore space that
exists between the structural aggregates, or “peds”, that make up a particular
soil horizon. The shape and arrangement of the peds dictates the size and
continuity of the pores. Typically, angular blocky, subangular blocky, and
granular structure create large pores that allow water to move through the soil.
Prismatic and platy structures have long but narrow pores that tend to slow down
vertical water movement.

Some soils contain a hydraulically restrictive horizon, such as a fragipan or
clay layer, that can impede the vertical movement of water down through the
soil. Water that is held up by a hydraulically restrictive horizon is called a
“perched water table”. Soils that do not have a hydraulically restrictive
horizon present are considered to have a “regional water table” that extends
vertically without interruption.
- References: Buckman, N.G. 1990. The Nature and Properties of Soils. Macmillan
Publishing Company, NYC.
- Hillel, D. 1980. Fundamentals of Soil Physics. Academic Press Inc., Orlando,
FL.
Under ideal conditions, the pore space of a soil would be half filled with
soil water and half filled with soil air. When adequate soil air is present for
certain plant and microbial activities, the soil environment is “aerobic”.
Aerobic soil conditions promote:
- plant root respiration
- aerobic microbial reactions
- combustion or consumption of organic matter
A soil that has its pore space completely filled with water is said to be
“saturated”. Prolonged periods of saturation result in the depletion of oxygen
by plants and microorganisms in the soil. If a soil remains saturated long
enough for all the oxygen to be depleted, the soil environment is “anaerobic”.
Anaerobic soil conditions promote:
- transformation of elements from an oxidized to a reduced form
(oxidation-reduction reactions)
- anaerobic microbial reactions
- accumulation of organic matter
In mineral soils, anaerobic conditions bring about a sequence of
oxidation-reduction (electron transfer) reactions. The microbial breakdown of
soil organic matter is an oxidation-reduction process. Under aerobic conditions,
organic matter is oxidized (loses electrons), and oxygen (O2) is reduced (gains
electrons) and combines with hydrogen to form water. The ultimate product of
aerobic degradation is CO2. When the soil becomes saturated, the amount of
oxygen is decreased; with continued breakdown of organic matter the oxygen can
be all used up, and the soil becomes anaerobic. Biodegradation of organic matter
now continues under different conditions; different groups of microbes go to
work using different electron acceptors instead of oxygen. These processes are
not as efficient or as complete as the aerobic one. Nitrates, manganese oxides,
iron oxides, and sulfates are soil compounds that are used as electron acceptors
in anaerobic microbial reactions, in a specific order. After the removal of
oxygen, nitrate is the first soil compound to be reduced; then manganese, iron,
and eventually sulfate are reduced. These transformations bring about the
translocation and/or accumulation of these elements, which can result in
morphological features useful in the identification of saturated zones in soil.
Nitrogen transformations in saturated soils can make the nutrient less
available for plant uptake. However, excessive amounts of nitrate (NO3-), the
mobile form of nitrogen, can be reduced to prevent leaching losses.
Manganese transformations are similar to iron in that manganic (Mn+4)
compounds are reduced to more soluble manganous (Mn+2) forms. Re-oxidized and
re-deposited manganic oxides appear as black films or coats on soil particles.
Oxidized or ferric (Fe+3) iron compounds are responsible for the brown,
yellow, and red colors in soil. When iron is reduced to the ferrous (Fe+2) form,
it becomes mobile, and can be removed from certain areas of the soil. When the
iron is removed, a gray color remains, or the reduced iron color persists in
shades of green or blue. Upon aeration, reduced iron can be re-oxidized and
re-deposited, sometimes in the same horizon, resulting in a variegated or
mottled color pattern. These soil color patterns resulting from saturation, or
“redoximorphic features”, can indicate the duration of the anaerobic state,
ranging from brown with a few mottles, to complete gray or “gleization” of the
soil. Soils that are dominantly gray with brown or yellow mottles immediately
below the surface horizon are usually hydric.
Sulfates in soils are reduced to sulfides when soils are nearly permanently
saturated. The presence of hydrogen sulfide can be detected by the “rotten egg”
odor, which is used as a hydric soil indicator. Sulfides can be toxic to
microbes and plants, and upon re-oxidation, can lead to extremely acid
conditions in soils when sulfuric acid is formed.
Hydric Soils of the US
This website includes a listing of New Jersey hydric soils and Field
Indicators of Hydric Soils in the US, A Guide for Identifying and Delineating
Hydric Soils.
Reference: Mitsch, W.J. and J.G. Gosselink. 1986. Wetlands. Van Nostrand
Reinhold, NYC.
Properties
- firm, brittle subsurface horizon that restricts plant root penetration
and downward water movement
- responsible for “perched” water tables in some soils
- not cemented by any of the common soil cementing agents (calcium
carbonate, iron, or silica)
- identified in soils descriptions with the horizon designation suffix
“x”; examples are Bx, Btx, Btxg
- tend to form in transported materials such as till, outwash, alluvium,
colluvium, and marine sediments
- the vertical extent of a fragipan can be continuous, where it gets more
dense and has less structure with depth; or discontinuous, where it “dies
out” or terminates abruptly, and can be underlain by friable and/or
permeable material
Morphology
- commonly has prismatic structure with visible prisms
- can also have platy, blocky, or massive structure
- prisms typically have high chroma matrix colors (chroma > 2); prism
faces commonly have high chroma redoximorphic features and the spaces
between prisms commonly are low chroma soil colors (chroma ≤ 2)
Identification in the field
Peds or pieces broken out of a fragipan should have the following
characteristics:
- firm or very firm moist consistence
- brittle manner of failure when moist; peds or pieces “explode” rather
than deform
- “slake” (disintegrate or dissolve) when immersed in water; this test
verifies that the horizon is not cemented
In Soil Taxonomy, a soil horizon is considered a fragipan if more than 50
percent of air dry fragments of the horizon slake in water. Also, 60 percent or
more of the horizon must have a firm or firmer rupture-resistance class, a
brittle manner of failure, and virtually no roots present. An additional test is
that the layer must not effervesce in dilute HCl, which is evidence that the
horizon is cemented by calcium carbonate.
< Back to Introduction
Last Modified:
May 27, 2008
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