Effects of dissolved organic carbon on sorption and mobility of imidacloprid in soil

To evaluate the effects of dissolved organic carbon on sorption and mobility of the insecticide imidacloprid [1-(6-chloro-3-pyridinyl) methyl-N-nitro-2-imidazolidinimine] in soils, adsorption and column experiments were performed by using a typical calcareous soil from southeastern Spain and two different types of dissolved organic carbon, that is, dissolved organic carbon extracts from a commercial peat (DOC-PE) and high-purity tannic acid (DOC-TA). The experiments were carried out from a 0.01 M CaCl2 aqueous medium at 25 degrees C. The results obtained from the sorption experiments show that the presence of both DOC-PE and DOC-TA, over a concentration range of 15 to 100 mg L(-1), produces in all cases a decreasing amount of imidacloprid adsorbed in the soil studied. From the column experiments the retardation coefficients (RC) were calculated for imidacloprid by using either 0.01 M CaCl2 aqueous solution (RC = 2.10), 0.01 M CaCl2 DOC-PE solution (RC = 1.65), or 0.01 M CaCl2 DOC-TA solution (RC = 1.87). The results indicate that mobility of imidacloprid is increased 21.4 and 11.0% in the presence of DOC-PE and DOC-TA solutions, respectively. Dissolved organic carbon reduces imidacloprid sorption by competing with the pesticide molecules for sorption sites on the soil surface, allowing enhanced leaching of imidacloprid and potentially increasing ground water contamination.     

Preferential bromide and pesticide movement to tile drains under different cropping practices

Subsurface drainage systems are useful tools to study chemical leaching in soils. Our objective was to compare the breakthrough behavior of bromide, atrazine (2-chloro-4-ethylamino-6-isopropylamino-s-triazine) and metolachlor [2-chloro-N-(2-ethyl-6-methylphenyl)-N-(2-methoxy-1-methylethyl) acetamid] to tile drains under two fall tillage practices (conventional tillage [CT] with a moldboard plow, and reduced tillage [RT] with a chisel plow) in field plots cultivated with corn (Zea mays L.). Leachate volume were greater in RT than in CT, with no statistical differences. Soil analysis showed that bromide migrated deeper in the soil profile than both herbicides, with little tillage effect. All chemicals were detected in drainage water at the same time and followed an event-driven behavior. Tillage had no effect on atrazine and metolachlor found in drainage water, while bromide concentration peaks were higher in RT than in CT in 1999. Concentration peaks were recorded earlier for atrazine and metolachlor than for bromide. Plots of cumulative relative chemical mass (cumulative mass divided by total mass measured in drainage) as a function of cumulative drainage were mostly linear for bromide, while they were S-shaped for both herbicides. Drainage that corresponded to 50% of relative cumulative mass ranged from 40 to 55% for bromide and from 5 to 28% for both herbicides. Rapid chemical movement to tile drains suggested that preferential flow was important in both CT and RT, and that these tillage practices had little influence on this phenomena.     

Laboratory and lysimeter studies of glyphosate and aminomethylphosphonic acid in a sand and a clay soil

Due to the increasing concern about the appearance of glyphosate [N-(phosphonomethyl)glycine] and its major metabolite aminomethylphosphonic acid (AMPA) in natural waters, batch laboratory and lysimeter transport studies were performed to assess the potential for leaching of the compounds in two agricultural soils. Unlabeled and 14C-labeled glyphosate were added at a rate corresponding to 1.54 kg a.i. ha(-1) on undisturbed sand and clay columns. Leachate was sampled weekly during a period of 748 d for analyses of glyphosate, AMPA, total 14C, and particle-bound residues. Topsoil and subsoil samples were used for determination of glyphosate adsorption, glyphosate degradation, and formation of AMPA and its degradation. The influence of adsorption on glyphosate degradation was confirmed, giving very slow degradation rate in the clay soil (half-life 110-151 d). The kinetics of AMPA residues suggest that although AMPA is always more persistent than glyphosate when formed from glyphosate, its degradation rate can be faster than that of glyphosate. The kinetics also suggest that apart from glyphosate being transformed to AMPA, the sarcosine pathway can be just as significant. The long persistence of glyphosate was also confirmed in the lysimeter study, where glyphosate+AMPA residues constituted 59% of the initial amount of glyphosate added to the clay soil 748 d after application. Despite large amounts of precipitation in the autumn and winter after application, however, these residues were mainly located in the topsoil, and only 0.009 and 0.019% of the initial amount of glyphosate added leached during the whole study period in the sand and clay, respectively. No leaching ofAMPA occurred in the sand, whereas 0.03 g ha(-1) leached in the clay soil.     

Effects of commercial diazinon and imidacloprid on microbial urease activity in soil and sod

Diazinon [O,O-diethyl O-2-isopropyl-6-methyl(pyrimidine-4-yl) phosphorothioate] and imidacloprid [1-(1-[6-chloro-3-pyridinyl]methyl)-N-nitro-2-imidazolidinimine] are applied to lawns for insect control simultaneously with nitrogenous fertilizers such as urea, but their potential effect on urease activity and nitrogen availability in turfgrass management has not been evaluated. Urease activity in enzyme assays, washed cell assays, and soil slurries was examined as a function of insecticide concentration. Intact cores from field sites were used to assess the effect of insecticide application on urease activity in creeping bentgrass (Agrostis palustris Huds.) and bluegrass (Poa pratensis L.) sod. Bacterial urease from Bacillus pasteurii and plant urease from jack bean [Canavalia ensiformis (L.) DC.] were unaffected by the insecticides. Both insecticides inhibited the growth of Proteus vulgaris, a urease-producing bacterium, but only diazinon significantly reduced urease activity in washed cells; neither insecticide inhibited urease activity in sonicated cells. Neither diazinon nor imidacloprid inhibited urease activity in Woolper soil (fine, mixed, mesic Typic Argiudoll) slurries, but diazinon slightly inhibited urease activity in Maury soil (fine, mixed, semiactive, mesic Typic Paleudalf) slurries. Imidacloprid had no effect on urease activity in creeping bentgrass or bluegrass sod at up to 10 times the commercial application rate. Diazinon briefly, but significantly, reduced urease activity in bluegrass sod. Co-application of imidacloprid and urea appears to be benign with respect to urease activity in soil and sod. Diazinon, in contrast, appears to have a significant, short-term, inhibitory effect on the microbial urease-producing community, but that effect depends on soil type.     

Water and nutrient transport on a heavy clay soil in a fluvial plain in the Netherlands

In flat areas, transport of dissolved nutrients by water through the soil matrix to groundwater and drains is assumed to be the dominant pathway for nutrient losses to ground- and surface waters. However, long-term data on the losses of nutrients to surface water and the contribution of various pathways is limited. We studied nutrient losses and pathways on a heavy clay soil in a fluvial plain in The Netherlands during a 5-yr period. Average annual nitrogen (N) and phosphorus (P) losses to surface water were 15.1 and 3.0 kg ha(-1) yr(-1), respectively. Losses were dominated by particulate N (50%) and P (70%) forms. Rapid discharge through trenches was the dominant pathway (60-90%) for water and nutrient transport. The contribution of pipe drains to the total discharge of water and nutrients was strongly related to the length of the dry period in the preceding summer. This relationship can be explained by the very low conductivity of the soil matrix and the formation of shrinkage cracks during summer. Losses of dissolved reactive P through pipe drains appear to be dominated by preferential flow based on the low dissolved reactive P concentration in the soil matrix at this depth. Rainfall occurring after manure application played an important role with respect to the annual losses of N and P in spring when heavy rainfall occurred within 2 wk after manure application.     

Movement of diuron and hexazinone in clay soil and infiltrated pond water

Pre-emergence herbicide residues were detected in domestic wells sampled near Tracy, CA. This study sought to determine the source of contamination by comparing soil distribution of diuron [N'-(3,4-dichlorophenyl)-N,N-dimethylurea] and hexazinone [3-cyclohexyl-6-(dimethylamino)-1-methyl-1,3,5-triazine-2,4(1H,3H)-dione] in an agricultural field where the soil was a cracking clay to infiltration of residues in water captured by an adjacent holding pond. Diuron and hexazinone were applied in December to a 3-yr-old alfalfa (Medicago sativa L.) crop. Water content of soil taken after major rainfall but before irrigation at 106 d after application was elevated at the lowest depth sampled centered at 953 mm, indicating water was available for percolation. Herbicide residues (reporting limit 8 microg kg(-1)) were confined above the 152 mm soil depth, even after subsequent application of two border-check surface irrigations. The pattern of distribution and concentration of residues in the soil were similar to results obtained from the LEACHM model, suggesting that macropore flow was limited to a shallow depth of soil. Herbicide residues were measured in runoff water at the first irrigation at 20 microg L(-1) for diuron and 1 microg L(-1) for hexazinone. Runoff water captured in the pond rapidly infiltrated into the subsurface soil, causing a concomitant rise in ground water elevation near the pond. Herbicide residues were also detected in the sampled ground water. We concluded that the pond was the predominant source for movement to ground water. Since addition of a surfactant to the spray mixture did not reduce concentrations in runoff water, mitigation methods will focus on minimizing infiltration of water from the pond.     

Degradation of endosulfan in a clay soil from cotton farms of western Queensland.

The persistence and degradation of endosulfan isomers and their primary degradation product, endosulfan-sulfate, were studied in a clay soil from cotton farms of western Queensland. Endosulfan degradation in relation to soil moisture, temperature, day and night temperature fluctuation, waterlogging and re-application were studied. The results show that the degradation rates of both endosulfan isomers were greatly affected by changes in soil water content and temperature. Under a high water content-high temperature regime the concentration of alpha-endosulfan in the soil fell rapidly during the first 4 weeks of application, followed by a prolonged period of slower rate of degradation. Alpha endosulfan showed a bi-exponential form of degradation for all water content-temperature experiments except for extremes in both these two factors. In the submerged soils (and also in low-water content, low temperature, non-submerged experiments) no such rapid initial degradation of alpha-endosulfan was observed, and a single first-order rate equation describes the data. Degradation of beta-endosulfan was significantly slower than for the alpha-isomer under all conditions studied. A half-life of more than a year was recorded for the beta-isomer when both water content and temperature were low. The degradation of beta-endosulfan showed no sign of the bi-exponential function observed for alpha-isomer, and a single first order rate equation described the data obtained for each factor studied. Endosulfan-sulfate was the major degradation product in all non-submerged experiments. Its build up in the soil very closely followed the disappearance of alpha-endosulfan. Its highest build-up was in the high water content-low temperature experiments, but its persistence was primarily influenced by soil temperature. Both alpha and beta-isomers, and endosulfan sulfate, persisted longer in the submerged soil. Re-application of endosulfan, and day and night fluctuation of temperature had contrasting effects on the degradation of the two isomers. Both factors slowed down the degradation of alpha-endosulfan and enhanced that of beta-endosulfan, but their net effect was to prolong the overall persistence of this chemical in the soil. Submerged conditions reduced the net formation of endosulfan-sulfate and enhanced its degradation rate.     

Hydrological properties of a clay loam soil after long-term cattle manure application

Limited information exists on the effect of long-term application of beef cattle (Bos taurus) manure on soil hydrological properties in the Great Plains region of North America. A site on a clay loam soil (Typic Haploboroll) was used to examine the effect of manure addition on selected soil hydrological properties in 1997 and 1998. The manure was annually applied in the fall for 24 yr at one, two, and three times the recommended rates (in 1973) under dryland (0, 30, 60, and 90 Mg ha(-1) wet basis) and irrigation (0, 60, 120, and 180 Mg ha(-1)). Manure significantly (P < or = 0.05) increased soil water retention (0-5 and 10-15 cm) by 5 to 48% compared with the control at most potentials between 0 and -1500 kPa. Field soil water content (0-5 and 10-15 cm) was increased by 10 to 22% in the summers of 1997 and 1998. Manure increased ponded infiltration by more than 200% at 90 Mg ha(-1) under dryland (1998) and at rates > or = 120 Mg ha(-1) under irrigation (1997). Field-saturated hydraulic conductivity (Kfs) of surface soil (1-cm depth) was significantly increased by 76 to 128% under dryland (1998) and irrigation (1997), as were number of pores > 1120 microm in diameter (37-128% increase). In contrast, manure rate had little or no effect on unsaturated hydraulic conductivity [K(psi)] values (-0.3, -0.5, -0.7, and -1.0 kPa) in 1997 and 1998. Overall, soil hydrological parameters generally had a neutral or positive response to 24 yr of annual manure addition.     

Fate of nitrate and bromide in an unsaturated zone of a sandy soil under citrus production

Understanding water and nutrient transport through the soil profile is important for efficient irrigation and nutrient management to minimize excess nutrient leaching below the rootzone. We applied four rates of N (28, 56, 84, and 112 kg N ha(-1); equivalent to one-fourth of annual N rates being evaluated in this study for bearing citrus trees), and 80 kg Br- ha(-1) to a sandy Entisol with >25-yr-old citrus trees to (i) determine the temporal changes in NO3-N and Br- distribution down the soil profile (2.4 m), and (ii) evaluate the measured concentrations of NO3-N and Br- at various depths with those predicted by the Leaching Estimation and Chemistry Model (LEACHM). Nitrate N and Br concentrations approached the background levels by 42 and 214 d, respectively. Model-predicted volumetric water content and concentrations of NO3-N and Br- at various depths within the entire soil profile were very close to measured values. The LEACHM data showed that 21 to 36% of applied fertilizer N leached below the root zone, while tree uptake accounted for 40 to 53%. Results of this study enhance our understanding of N dynamics in these sandy soils, and provide better evaluation of N and irrigation management to improve uptake efficiency, reduce N losses, and minimize the risk of ground water nitrate contamination from soils highly vulnerable to nutrient leaching.     

Visualizing bromide and iodide water tracer in soil profiles by spray methods

In this study we developed and tested a spray method to visualize bromide water tracer in soil profiles. The method is based on the transformation reaction of a white precipitate into a colored one (Prussian blue) in the presence of Br-. After application of water containing bromide (0.2-0.4% wt.), a soil profile is dug out from the irrigated area and sprayed with a Br- indication suspension containing ferric ion and silver ferrocyanide precipitate. About two hours later, the pattern of irrigation water movement in the soil profile appears due to the formation of Prussian blue complex. We describe the method and demonstrate its use in a field experiment to visualize water flow paths. Since this method might be subject to possible interference from Cl-, a newly designed method with iodide ion as a water tracer and its indication solution containing soluble starch and ferric ion is also presented and recommended for use in soils with high chloride background.     

Imazaquin adsorbed on pillared clay and crystal violet-montmorillonite complexes for reduced leaching in soil

Ground water pollution due to herbicide leaching has become a serious environmental problem. Imazaquin [2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)quinoline-3-carboxylic acid] is an herbicide used to control broadleaf weeds in legume crops. Imazaquin is negatively charged at the basic pH of calcareous soils and exhibits high leaching potential in soils. Our aim was to design formulation of imazaquin to reduce herbicide leaching. Imazaquin sorption on pillared clay (PC) and crystal violet (CV)-montmorillonite complexes was studied. The CV-montmorillonite complexes become positively charged with adsorption of CV above the cation exchange capacity (CEC) of montmorillonite, and thus can sorb imazaquin. The Langmuir equation provides a good fit to isotherms of imazaquin sorption on PC and CV-montmorillonite complexes, but for charged complexes an equation that combines electrostatics with specific binding was preferred. Maximal imazaquin sorption was 17.3 mmol kg-1 for PC and 22.2 mmol kg-1 for CV-montmorillonite complexes. The extents of imazaquin desorption into water were 21% for PC and 5% for CV-clay complexes. The presence of anions decreased imazaquin sorption on both sorbents in the sequence phosphate > acetate > sulfate. Reduction of imazaquin sorption by the anions and the extent of its desorption in electrolyte solutions were higher for PC than for CV-clay complexes. Leaching of imazaquin from CV-montmorillonite formulations through soil (Rhodoxeralf) columns was two times less than from PC formulations and four times less than that of technical imazaquin. The CV-montmorillonite complexes at a loading above the CEC appear to be suitable for preparation of organo-clay-imazaquin formulations that may reduce herbicide leaching significantly.     

Differences in microbial biomass,organic carbon,and dye sorption between flow and no-flow regions of unsaturated soil

Transport models in which the liquid phase is partitioned between conducting and nonconducting regions allow the possibility that degradation and sorption are different in these regions. However, there is little information on biological or chemical differences between conducting and nonconducting regions of the soil matrix. Previous work by the authors on Br transport through unsaturated, intact soil cores of Dundee silty clay loam (fine-silty, mixed, active, thermic Typic Endoaqualf) indicated non-equilibrium conditions that could be well-described by a two-region model. Fitted parameters indicated little solute transfer between flow regions, suggesting that dye movement in unsaturated soil might delineate conducting and nonconducting regions of this soil. Steady-state, unsaturated flow was established in intact cores (10 by 30 cm) of the Dundee soil, then Br and erioglaucine dye were displaced through these cores. The soil cores were then sectioned into 5-cm segments and stained soil was separated from unstained soil. Microbial biomass C, organic C, and dye sorption K(D) (= g(sorbed) kg(-1)soil/g L(-1)) values for stained and unstained soil were determined. Stained soil had higher microbial biomass C but generally lower organic C and lower affinity for dye sorption than unstained soil from the same depth increment. Fraction of immobile water, dispersion, and mass transfer between conducting and nonconducting regions were consistent with previous results.     

Transport of sulfadiazine in undisturbed soil columns: effects of flow rate, input concentration and pulse duration

Antibiotics reach soils via spreading of manure or sewage sludge. Knowledge on the transport behavior of antibiotics in soils is needed to assess their environmental fate. The effect of flow rate and applied mass, i.e., input concentration and pulse duration, on the transport of 14C-sulfadiazine (SDZ; 4-aminoN-pyrimidin-2-yl-benzenesulfonamide) was investigated with soil column experiments and numerical studies. Sulfadiazine was applied in pulses (6.8, 68 or 306 h) under steady-state (0.051 and 0.21 cm h(-1)) and intermittent flow conditions and at two input concentrations (0.57 and 5.7 mg L(-1)). Breakthrough curves (BTCs) of 14C were measured and for one experiment concentrations of SDZ, and its transformation products 4-(2-iminopyrimidin-1(2H)-yl)aniline (An-SDZ) and N(1)-2-(4-hydroxypyrimidinyl)benzenesulfanilamide (4-OH-SDZ) were determined. After finalizing the leaching experiments, 14C was quantified in different slices of the columns. A lower flow rate led to remarkably lower eluted masses compared with the higher flow rates. All BTCs could be described well using a three-site attachment-detachment model for which a common set of parameters was determined. However, the BTC obtained with the high input concentration was slightly better described with a two-site isotherm-based model. The prediction of the concentration profiles was good with both model concepts. The fitted sorption capacities decreased in the order SDZ > 4-OH-SDZ > An-SDZ. Overall, the experiments reveal the presence of similar mechanisms characterizing SDZ transport. The dependence of model performance on concentration implies that although the three-site attachment-detachment model is appropriate to predict the transport of SDZ in soil columns, not all relevant processes are adequately captured.     

The effects of soil carbon on phosphorus and sediment loss from soil trays by overland flow

Soil chemical constituents influence soil structure and erosion potential. We investigated manure and inorganic fertilizer applications on soil chemistry (carbon [C] quality and exchangeable cations), aggregation, and phosphorus (P) loss in overland flow. Surface samples (0-5 cm) of a Hagerstown (fine, mixed, semiactive, mesic Typic Hapludalf) soil, to which either dairy or poultry manure or triple superphosphate had been applied (0-200 kg P ha(-1) yr(-1) for 5 yr), were packed in boxes (1 m long, 0.15 m wide, and 0.10 m deep) to field bulk density (1.2 g cm(-3)). Rainfall was applied (65 mm h(-1)), overland flow collected, and sediment and P loss determined. All amendments increased Mehlich 3-extractable P (19-177 mg kg(-1)) and exchangeable Ca (4.2-11.5 cmol kg(-1)) compared with untreated soil. For all treatments, sediment transport was inversely related to the degree of soil aggregation (determined as ratio of dispersed and undispersed clay; r = 0.51), exchangeable Ca (r = 0.59), and hydrolyzable carbohydrate (r = 0.62). The loss of particulate P and total P in overland flow from soil treated with up to 50 kg P ha(-1) dairy manure (9.9 mg particulate phosphorus [PPI, 15.1 mg total phosphorus [TP]) was lower than untreated soil (13.3 mg PP, 18.1 mg TP), due to increased aggregation and decreased surface soil slaking attributed to added C in manure. Manure application at low rates (<50 kg P ha(-1)) imparts physical benefits to surface soil, which decrease P loss potential. However, at greater application rates, P transport is appreciably greater (26.9 mg PP, 29.5 mg TP) than from untreated soil (13.3 mg PP, 18.1 mg TP).     

Using soil moisture and spatial yield patterns to identify subsurface flow pathways

Subsurface soil water dynamics can influence crop growth and the fate of surface-applied fertilizers and pesticides. Recently, a method was proposed using only ground-penetrating radar (GPR) and digital elevation maps (DEMs) to identify locations where subsurface water converged into discrete pathways. For this study, the GPR protocol for identifying horizontal subsurface flow pathways was extended to a 3.2-ha field, uncertainty is discussed, and soil moisture and yield patterns are presented as confirming evidence of the extent of the subsurface flow pathways. Observed soil water contents supported the existence of discrete preferential funnel flow processes occurring near the GPR-identified preferential flow pathways. Soil moisture also played a critical role in the formation of corn (Zea mays L.) grain yield patterns with yield spatial patterns being similar for mild and severe drought conditions. A buffer zone protocol was introduced that allowed the impact of subsurface flow pathways on corn grain yield to be quantified. Results indicate that when a GPR-identified subsurface clay layer was within 2 m of the soil surface, there was a beneficial impact on yield during a drought year. Furthermore, the buffer zone analysis demonstrated that corn grain yields decreased as the horizontal distance from the GPR-identified subsurface flow pathways increased during a drought year. Averaged real-time soil moisture contents at 0.1 m also decreased with increasing distance from the GPR-identified flow pathways. This research suggests that subsurface flow pathways exist and influence soil moisture and corn grain yield patterns.     

Cadmium, copper, nickel, and zinc availability in a biosolids-amended piedmont soil years after application

Concerns over the possible increase in phytoavailability of biosolids-applied trace metals to plants have been raised based on the assumption that decomposition of applied organic matter would increase phytoavailability. The objectives of this study were to assess the effect of time on chemical extractability and concentration of Cd, Cu, Ni, and Zn in plants on plots established by a single application of biosolids with high trace metals content in 1984. Biosolids were applied to 1.5 by 2.3 m confined plots of a Davidson clay loam (clayey, kaolinitic, thermic Rhodic Kandiudults) at 0, 42, 84, 126, 168, and 210 Mg ha(-1). The highest biosolids application supplied 4.5, 760, 43, and 620 kg ha(-1) of Cd, Cu, Ni, and Zn, respectively. Radish (Raphanus sativus L.), romaine lettuce (Lactuca sativa L. var. longifolia), and barley (Hordeum vulgare L.) were planted at the site for 3 consecutive years, 17 to 19 yr after biosolids application. Extractable Cd, Cu, Ni, and Zn (as measured by DTPA, CaCl(2,) and Mehlich-1) were determined on 15-cm depth samples from each plot. The DTPA-extractable Cu and Zn decreased by 58 and 42%, respectively, 17 yr after application despite a significant reduction in organic matter content. Biosolids treatments had no significant effect on crop yield. Plant tissue metal concentrations increased with biosolids rate but were within the normal range of these crops. Trace metal concentrations in plants generally correlated well with the concentrations extracted from soil with DTPA, CaCl(2), and Mehlich-1. Metal concentrations in plant tissue exhibited a plateau response in most cases. The uptake coefficient values generated for the different crops were in agreement with the values set by the Part 503 Rule.     

Agricultural land use and soil degradation in a part of kwara state,Nigeria

Summary Because of the alarming rate of increase in population all over tropical Africa, and the consequent need to grow more food, several writers have suggested the practice of continuous or permanent cultivation in place of the traditional bush fallowing system. This suggestion has been made without recognising the natural vulnerability of tropical soils and the associated problems of actual soil degradation, especially in situations where fertilizer inputs are limited. This study examines the effects of different land use practices on actual soil degradation in a part of Kwara State, Nigeria. This involves comparing the physical and chemical properties of the soils in areas under continuous cultivation, fallow and forests, and using the technique of factor analysis to isolate indices which best describe these phenomena. The results show that the main effects of continuous cultivation in the area examined were to increase the acidity of the soil, that soil organic matter content was likely to double after 10 years of fallow conditions, and that continuous cultivation was capable of reducing the cation-exchange capacity of soils by at least one-third.In general, the soils of the area of study display marked variability, especially with respect to their chemical properties. This is mainly due to variations in soil organic matter content, which in itself is due to differences in agricultural land use practices. Factor analysis of the soil properties generated four main indices of actual soil degradation, of which organic matter is the most important. Some implications of the results are examined, particularly in relation to generating an awareness of actual soil degradation and land use planning.Dr J. Oluwole Ameyan, the senior author, is on the staff of the University of Ilorin. Mr O. Ogidiolu is at the Department of Geography, Ondo State University, Ado-Ekiti, Nigeria.     

Real-time, high-resolution quantitative measurement of multiple soil gas emissions: selected ion flow tube mass spectrometry

A new technique is presented for the rapid, high-resolution identification and quantification of multiple trace gases above soils, at concentrations down to 0.01 microL L(-1) (10 ppb). The technique, selected ion flow tube mass spectrometry (SIFT-MS), utilizes chemical ionization reagent ions that react with trace gases but not with the major air components (N2, O2, Ar, CO2). This allows the real-time measurement of multiple trace gases without the need for preconcentration, trapping, or chromatographic separation. The technique is demonstrated by monitoring the emission of ammonia and nitric oxide, and the search for volatile organics, above containerized soil samples treated with synthetic cattle urine. In this model system, NH3 emissions peaked after 24 h at 2000 nmol m(-2) s(-1) and integrated to approximately 7% of the urea N applied, while NO emissions peaked about 25 d after urine addition at approximately 140 nmol m(-2) s(-1) and integrated to approximately 10% of the applied urea N. The monitoring of organics along with NH3 and NO was demonstrated in soils treated with synthetic urine, pyridine, and dimethylamine. No emission of volatile nitrogen organics from the urine treatments was observed at levels >0.01% of the applied nitrogen. The SIFT method allows the simultaneous in situ measurement of multiple gas components with a high spatial resolution of < 10 cm and time resolution <20 s. These capabilities allow, for example, identification of emission hotspots, and measurement of localized and rapid variations above agricultural and contaminated soils, as well as integrated emissions over longer periods.     

Contamination time effect on lead and cadmium fractionation in a tropical coastal clay

The capability of a tropical coastal clay to immobilize lead (Pb) and cadmium (Cd) was investigated in laboratory batch sorption tests conducted under acidic, neutral, and slightly alkaline conditions. The contact time was extended to 65 d. The distribution of Pb and Cd among various sorbed phases was examined using a sequential extraction technique. The sorbed phases were fractionated into the exchangeable, carbonate, reducible, organic, and residual fractions. There were only small changes in the total Pb and Cd sorption beyond a 1-d sorption period. The metal fractionation results show that the amount of Pb and Cd in various fractions changed with sorption time, and the changes were pH-dependent. These changes could be attributed to mineral dissolution and transformation or redistribution of the sorbed phases. Transformation of the sorbed phases resulted in increasing Pb and Cd retention in the more persistent fractions with time, at the expense of reductions in the loosely bound fractions. Nevertheless, Pb and Cd fractionation in the solid phase appeared to reach equilibrium within the 65-d sorption period. These Pb and Cd fractionation results reflect the effect of contamination time on the heavy metal lability and bioavailability in the subsurface environment.