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Soil, transport through

Nonaqueous phase Hquids (NAPLs) present special problems for soil and ground water cleanup. Contaminant transport through ground water depends in part on the water solubiHty of the compound. Because NAPLs cling to subsurface particles and are slow to dissolve in ground water, they hinder cleanups and prolong cleanup times. Dense nonaqueous phase Hquids (DNAPLs) migrate downward in the aquifer and can coUect in pools or pockets of the substmcture. Examples of DNAPLs are the common solvents tetrachloroethylene (PCE) and trichloroethylene (TCE) which were used extensively at many faciHties before the extent of subsurface contamination problems was realized. [Pg.169]

Fig. 14-4 Schematic representation of the transport of P through the terrestrial system. The dominant processes indicated are (1) mechanical and chemical weathering of rocks, (2) incorporation of P into terrestrial biomass and its return to the soil system through decomposition, (3) exchange reactions between soil interstitial waters and soil particles, (4) cycling in freshwater lakes, and (5) transport through the estuaries to the oceans of both particulate and dissolved P. Fig. 14-4 Schematic representation of the transport of P through the terrestrial system. The dominant processes indicated are (1) mechanical and chemical weathering of rocks, (2) incorporation of P into terrestrial biomass and its return to the soil system through decomposition, (3) exchange reactions between soil interstitial waters and soil particles, (4) cycling in freshwater lakes, and (5) transport through the estuaries to the oceans of both particulate and dissolved P.
As reactive P is transported through the terrestrial system, it is assimilated into plants and subsequently into the rest of the biosphere (2). Although many elements are required for plant life, in many ecosystems P is the least available and, therefore, limits overall primary production (Schindler, 1977 Smith et al., 1986). Thus, in many instances the availability of P influences or controls the cycling of other bioactive elements. When organisms die, the organic P compounds decompose and the P is released back into the soil-water system. This cycle of uptake and release may be repeated numerous times as P makes its way to the oceans. [Pg.365]

Since our principal interest in P. hysterophorus has been to identify the chemicals involved in the allelopathy, we have employed water as the extraction media for the plant material. Presumably, in the environment, chemicals extruded by P hysterophorus find their way to neighboring plants by transport through the water in the soil. [Pg.150]

This section discusses soil liners and their use in hazardous waste landfills. The section focuses primarily on hydraulic conductivity testing, both in the laboratory and in the field. It also covers materials used to construct soil liners, mechanisms of contaminant transport through soil liners, and the effects of chemicals and waste leachates on compacted soil liners. [Pg.1102]

Groot IT, van Bodegom PM, Meijer HAJ, Harren FJM. Gas transport through the root-shoot transition zone of rice tillers. Plant Soil. 2005 277 107-116. [Pg.206]

Yu KW, Wang ZP, Chen GX. Nitrous oxide and methane transport through rice plants. Biol. Fertil. Soils. 1997 24 341-343. [Pg.206]

Valocchi, A.J., 1985, Validity of the local equilibrium assumption for modeling sorbing solute transport through homogeneous soils. Water Resources Research 21, 808-820. [Pg.532]

Arsenic leaches from the base of the ARS, transports through the underlying clayey soil, and into the underlying aquifer producing the high concentration in MW17. [Pg.374]

If a pesticide, or any other solute, is sprayed onto the field it will travel in the water through the soil, but may also be adsorbed onto the soil. It is assumed that the process of adsorption occurs almost instantaneously, as compared to the slower rate of transport through the soil. Only solute dissolved in the mobile water column is transported from one element to the next. [Pg.587]

In practise some water will always be transported through the soil even if the local water content is less than the field capacity owing to preferential flow through cracks and large pores in the soil structure. This can be modelled simply by defining a bypass parameter to account for the fraction of water that can pass through each element. Modify the model to include bypass and see how this influences the solute profiles (see Corwin et al. (1991) for further details). [Pg.589]

Jaquess AB, WinterlinW, Peterson D. 1989. Feasibility of toxaphene transport through sandy soil. Bull Environ Contain Toxicol 42 417-423. [Pg.180]

Disulfoton is also transported through soils or from soil to surface water (streams or rivers) via runoff. Pesticides with water solubilities >10 mg/L move mainly in solution phase in runoff water (Racke 1992). Disulfoton, with a water solubility of 25 mg/L (Sanborn et al. 1977), is expected to be found mainly in runoff water. In a runoff event from agricultural soil in Nebraska, low levels of disulfoton were detected both in the dissolved state and in eroding soil particles in the sorbed state (Spalding and Snow 1989). [Pg.147]

Sorption/desorption is the key property for estimating the mobility of organic pollutants in solid phases. There is a real need to predict such mobility at different aqueous-solid phase interfaces. Solid phase sorption influences the extent of pollutant volatilization from the solid phase surface, its lateral or vertical transport, and biotic or abiotic processes (e.g., biodegradation, bioavailability, hydrolysis, and photolysis). For instance, transport through a soil phase includes several processes such as bulk flow, dispersive flow, diffusion through macropores, and molecular diffusion. The transport rate of an organic pollutant depends mainly on the partitioning between the vapor, liquid, and solid phase of an aqueous-solid phase system. [Pg.296]

Apart from the economic significance of such loss there are potentially adverse effects on the environment arising from acidification of rain and soil. Ammonia may react with hydroxyl radicals in the atmosphere to produce NOx contributing to the acidification of rain (4). Wet and dry deposition of NH3/NH4+ inevitably contributes to soil acidification through their subsequent nitrification. This effect can be accentuated in woodland by absorption of aerosols containing NH4+ within the canopy followed by transport to the soil in stem flow (5). In more extreme cases, NH3 emission from feedlots, pig and poultry... [Pg.36]

Watson, J., and P. Baker. (1990). Pesticide transport through soils. Tucson, Arizona Cooperative Extension, College of Agriculture, University of Arizona. [Pg.164]

Transport of solutes and gases through the soil is much slower than through soil-free water because of the restricted cross-sectional area for transport through the soil pore network and because of adsorption and reaction on soil surfaces (Chapter 2). Redox conditions are therefore closely linked to transport processes. [Pg.107]

To calculate the inflow, Cta must be found from the concentration in the soil bulk taking into account rates of transport through the soil. Kirk and Solivas (1997) have done this for N uptake by rice growing in flooded soil and used the resulting model to assess the relative importance of root uptake properties and transport through the soil. Their results are summarized in the following. [Pg.178]

The factors controlling the transport through soil include ... [Pg.218]

Ammonia has a lifetime of only a few hours to a few days in the atmosphere. It and its reaction products are transported through the atmosphere and deposited on terrestrial snrfaces elsewhere. It is the main gaseous alkaline species in the atmosphere and neutralizes a large part of the acid produced in oxidation of sulfur and nitrogen oxides, probably up to a half though its dry-deposition is much faster than that of NO and SO2 (Dentener and Crutzen, 1994). Dry- and wet-deposition of ammonia contribute to soil acidification because 2 mol of H+ are produced in the nitrification of Imol of NH4+. Also a large part of the ammonia deposited on moist forest soils may be re-emitted as N2O (Section 8.2). [Pg.252]

Kirk GJD, Solivas JL. 1997. On the extent to which root properties and transport through the soil limit nitrogen uptake by lowland rice. European Journal of Soil Science 48 613-621. [Pg.269]

Vinten et al. (1983) demonstrated that the vertical retention of contaminated suspended particles in soils is controlled by the soil porosity and the pore size distribution. Figure 5.8 illustrates the fate of a colloidal suspension in contaminated water during transport through soil. Three distinct steps in which contaminant mass transfer may occur can be defined (1) contaminant adsorption on the porous matrix as the contaminant suspension passes through subsurface zones, (2) contaminant desorption from suspended solid phases, and (3) deposition of contaminated particles as the suspension passes through the soil. [Pg.118]

Fig. 12.18A shows the results of an experiment using " C-labeled paraquat adsorbed on a clay mineral (Li-montmorillonite) suspension through a soil column. When the suspension medium was distilled water, 50% of the pesticides penetrated beyond 12 cm. Under these conditions, clay remains dispersed and pestieide is readily transported through the soil. However, for a suspension medium with an electrolyte concentration of 1 mM CaCl, paraquat remains in the upper 1 cm layer. The high calcium concentration results in rapid immobilization of the clay in the soil through flocculation, and consequently little pesticide transport occurs. [Pg.268]


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See also in sourсe #XX -- [ Pg.273 ]




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