Schätzung der Denitrifikation in landwirtschaftlich genutzten Böden. I. Grundlagen

Estimating denitrification in agricultural soils: I. Basic assumptions Despite a common interest of soil scientists, groundwater hydrologists, agronomists, and climatologists in quantifying soil nitrogen losses through denitrification, these are often neglected when the nitrogen turnover of agricultural soils is modelled. This is the first of two papers describing a semi-quantitative denitrification model that has been derived from data collected from soils of a catchment area near Viersen in the Lower Rhine Valley in West Germany. A field study was conducted to study the soil environment of denitrifying microorganisms. The results of this study were used to evaluate the effect of soil water, soil air and soil temperature, of the amount and quality of the organic matter, and of the pH-value on denitrification. To this end an existing model to quantify denitrification was extended. Provided the seasonal nitrogen excess of a field is known, the model in its new form enables an estimation of the extent of field-specific denitrification rates. This paper describes the effects of the parameters under consideration on denitrification, the model components used to describe these parameters, and the development of the denitrification model.     

Adsorption of Acrylonitrile on Some Soils and Minerals from Aqueous Solutions

Equilibrium and kinetic studies have been made on the adsorption of acrylonitrile(CH2=CHCN) on three soils and four minerals from aqueous solutions.It was shown that the organic matter was the major factor affecting the adsorption process in the soils.The conformity of the equilibrium data to linear type(one soil) and Langmuir type(two soils) isotherms indicated that different mechanisms were involved in the adsorption.This behavior appears bo be related to the hydrophobicity of soil organic matter due to their composition and E4/E6 ratio of humic acids.The adsorption kinetics were also different among the soils,indicating the difference in porosity of organic matter among the soils,and the kinetics strongly affected the adsorption capacity of soils for acrylonitrile.Acrylonitrile was slightly adsorbed from aqueous solutions on pyrophyllite with electrically neutral and hydrophobic nature,and practically not on montmorillonite and kaolinite saturated with Ca.However,much higher adsorption occurred on the zeolitized coal ash,probably caused by high organic carbon content(107g/kg).     

Denitrification potential of intermittently saturated floodplain soils from a subtropical perennial stream and an ephemeral tributary

Denitrification has the potential to remove excess nitrogen from groundwater passing through riparian buffers, thus improving water quality downstream. In regions with markedly seasonal precipitation, transient stream flow events may be important in saturating adjacent floodplain soils and intermittently providing the anaerobic conditions necessary for denitrification to occur. In two experiments we characterised the denitrification potential of soils from two contrasting floodplains that experience intermittent saturation. We quantified under controlled laboratory conditions: 1) potential rates of denitrification in these soils with depth and over time, for a typical period of saturation; and 2) the influences on rates of nitrate and organic carbon. Treatments differed between experiments, but in each case soil-water slurries were incubated anaerobically with differing amendments of organic carbon and nitrate; denitrification rates were measured at selected time intervals by the acetylene-block technique; and slurry filtrates were analysed for various chemical constituents. In the first experiment (ephemeral tributary), denitrification was evident in soils from both depths (0-0.3 m; 0.3-1.1 m) within hours of saturation. Before Day 2, mean denitrification rates at each depth were generally comparable, irrespective of added substrates; mean rates (Days 0 and 1) were 5.2 ± 0.3 mg N kg dry soil⁻¹ day⁻¹ (0-0.3 m) and 1.6 ± 0.2 mg N kg dry soil⁻¹ day⁻¹ (0.3-1.1 m). Rates generally peaked on Days 2 or 3. The availability of labile organic carbon was a major constraint on denitrification in these soils. Acetate addition greatly increased rates, reaching a maximum in ephemeral floodplain soils of 17.4 ± 1.8 mg N kg dry soil⁻¹ day⁻¹ on Day 2: in one deep-soil treatment (low nitrate) this overcame differences in rates observed with depth when acetate was not added, although the rate increase in the other deep-soil treatment (high nitrate) was significantly less (P ≤ 0.01). Without acetate, peak denitrification rates in this experiment were 6.9 ± 0.4 and 2.8 ± 0.2 mg N kg dry soil⁻¹ day⁻¹ in surface and deep soils, respectively. Differences in rates were observed with depth on all occasions, despite similar initial concentrations of dissolved organic carbon (DOC) at both depths. Levels of substrate addition in the second experiment (perennial stream) more closely reflected natural conditions at the site. Mean denitrification rates were consistently much higher in surface soil (P ≤ 0.001), while the source of water used in the slurries (surface water or groundwater from the site) had little effect on rates at any depth. Mean rates when all treatments retained nitrate were: 4.5 ± 0.3 mg N kg dry soil⁻¹ day⁻¹ (0-0.3 m depth); 0.8 ± 0.3 mg N kg dry soil⁻¹ day⁻¹ (0.3-1.0 m); and 0.6 ± 0.1 mg N kg dry soil⁻¹ day⁻¹ (1.8-3.5 m). For comparable treatments and soil depths, denitrification potentials at both sites were similar, apart from higher initial rates in the ephemeral floodplain soils, probably associated with their higher DOC content and possibly also their history of more frequent saturation. The rapid onset of denitrification and the rates measured in these soils suggest there may be considerable potential for nitrate removal from groundwater in these floodplain environments during relatively short periods of saturation.     

Relationships between the denitrification capacities of soils and total,water-soluble and readily decomposable soil organic matter

The relationships between the denitrification capacities of 17 surface soils and the amounts of total organic carbon, mineralizable carbon, and water-soluble organic carbon in these soils were investigated. The soils used differed markedly in pH, texture, and organic-matter content. Denitrification capacity was assessed by determining the N evolved as N₂ and N₂O on anaerobic incubation of nitrate-treated soil at 20°C for 7 days, and mineralizable carbon was assessed by determining the C evolved as CO₂ on aerobic incubation of soil at 20°C for 7 days. The denitrification capacities of the soils studied were significantly correlated (r = 0·7771) with total organic carbon and very highly correlated (r = 0·9971) with water-soluble organic carbon or mineralizable carbon. The amount of nitrate N lost on anaerobic incubation of nitrate-treated soils for 7 days was very closely related (r = 0·99971) to the amount of N evolved as N₂ and N₂O.The work reported indicates that denitrification in soils under anaerobic conditions is controlled largely by the supply of readily decomposable organic matter and that analysis of soils for mineralizable carbon or water-soluble organic carbon provides a good index of their capacity for denitrification of nitrate.     

Organic matter available for denitrification in different soil fractions: effect of freeze/thaw cycles and straw disposal

The 0 to 20-cm surface layer of a sandy loam soil was sampled in early autumn from plots where straw had either been removed or incorporated annually for 22 years. Denitrification in whole soils, 1–2-mm wet-stable aggregates, clay and silt size fractions was determined by acetylene blocking during anaerobic incubation with excess nitrate. Thus available organic matter was the limiting factor. Samples were exposed to one or two freeze/thaw cycles, or used unfrozen. K₂SO₄-extractable carbon (C) was determined before and after CHCI, fumigation. Freeze/thaw increased denitrification in whole soils and in aggregates. In aggregates and in whole soil without straw the increase in denitrification was similar following two freeze/thaw cycles, and well above the amount that could be fed by extractable soil C. In whole soils with straw addition, an extra denitrification increase occurred at first thaw only. This straw-induced denitrification surplus was matched by a decline in soil microbial biomass. For other samples and treatments, the freeze/thaw released C from additional organic matter sources. The availability of C in clay for denitrification was twice that of silt-associated C. Straw disposal generally had no effect on the bioavailability of particle-bound C. In contrast to whole soils and aggregates, the availability of organic matter in clay and silt after one freeze/thaw cycle was only half that observed from unfrozen samples. The effect of freeze/thaw on whole soils and aggregates may be to release organic matter available for denitrification by killing the microbial biomass and by disintegrating aggregates. However, the impact of freeze/thaw on completely dispersed samples such as clay and silt may be to promote the formation of granular structures (micro-aggregation) in which organic matter may become less accessible to denitrifiers.     

Schätzung der Denitrifikation in landwirtschaftlich genutzten Böden. II. Ergebnisse und Bewertung

Estimating denitrification in agriculturally used soils: II. Results and evaluation This is the second of two papers describing a denitrification model. Whereas in the first paper the model approach was described, the second paper deals with results obtained with the model. To evaluate the model's performance, 14 profiles in the catchment area of a water-work were studied in detail. For each site the potential and the actual annual denitrification rates were estimated. It was found that the least favorable conditions for denitrification occurred in the sandy soils of the study area. Consequently, estimated denitrification rates were lowest (< 10 kg N ha^?1 a^?1) in these soils. Estimated denitrification rates were highest (50 kg N ha^?1 a^?1) in peal and river plain soils, with either a high amount of organic matter and/or a high groundwater table. In silty loess soils, denitrification losses were estimated to be 20 to 35 kg N ha^?1 a^?1. With use of the anion concentrations in the surface layer of the groundwater, a plausibility study was conducted to evaluate the estimated denitrification losses. Its results show that the values obtained are realistic. However, a true calibration of the model is still necessary.     

Factors limiting denitrification in a Mediterranean riparian forest

In situ denitrification (DNT) and denitrification enzyme activity (DEA) were measured in a Mediterranean riparian forest soil during two periods under contrasting soil moisture conditions in order to investigate the factors that affect denitrification through the year. Results showed that in summer, soil moisture limited denitrification throughout the entire soil profile, whereas in winter, anaerobic conditions in the soil were more favourable for denitrifiers. The potential for denitrification was larger at shallow depths (<30 cm), and neither nitrate nor organic carbon limited denitrification significantly. Some denitrification was measured during winter at depths below 30 cm, suggesting that a reduction of groundwater nitrate could occur in some areas of this riparian forest during the wet period. In summer, low denitrification, together with high mineralization rates, brought about an increase of soil N, which could be leached to the stream channel during rainfall events. This study suggests that Mediterranean riparian soils act as sources or sinks of dissolved nitrogen depending on the period of the year.     

Factors affecting the availability of organic carbon for denitrification of nitrate in subsoils

Summary Recent work in our laboratory indicated that the slow rate of denitrification in Iowa subsoils is not due to a lack of denitrifying microorganisms, but to a lack of organic C that can be utilized by these microorganisms for reduction of nitrate. To identify factors affecting the availability of leachable organic C in surface soils capable of promoting denitrification in subsoils, we studied the effects of freezing and drying and of plants and plant residues on the amounts of water-soluble organic C in surface soils and the ability of this organic C to promote denitrification in subsoils. We found that aqueous extracts of field-moist, frozen, and air-dried surface soils promoted denitrification in subsoils and that their stimulatory effects on denitrification were highly correlated (r=0.93) with their organic C contents and decreased in the order air-dried soils frozen soils >field-moist soils. But a detailed study of the effect of drying a surface soil to different water tensions indicated that drying of soils under natural conditions is not likely to lead to a substantial increase in their content of water-soluble organic C. Amendment of surface soils with corn or soybean residues led to a marked increase in the amount of organic C in aqueous extracts of the soils and in the ability of these extracts to promote denitrification in subsoils. These effects of plant residues could not be detected after incubation of residue-treated soils for a few days under aerobic conditions, but they increased markedly with an increase in the time of incubation from 1 to 10 days when residue-treated soils were incubated under anaerobic conditions. Analyses for organic acids indicated that this increase was largely due to fermentative production of acetic, propionic, and butyric acids by soil microorganisms. Growth chamber studies showed that growth of corn, soybean, wheat, and sorghum plants on surface soil did not significantly increase the organic C content of leachates of the soil or the ability of these leachates to promote denitrification in subsois. We conclude that plant residues are a major source of the leachable organic C in surface soils that is capable of promoting denitrification in subsoils.     

Effects of organic solvents on denitrification in soil

Summary Although organic solvents such as methanol and ethanol have been shown to act as energy sources for denitrifying microorganisms, no studies on the influence of organic solvents on denitrification in soil have been reported. Organic solvents have been used as an aid in the application of pesticides and other agricultural chemicals to soil, in studying the effects of these chemicals on denitrification in soil. During these applications, the soil is often aerated or heated to remove the solvent while leaving the chemical in the soil. The work reported here shows that treating soils with methanol, ethanol, or acetone had a very marked effect on their denitrifying ability, even when the soils were aerated thoroughly or heated at 50°C to remove these solvents. This indicates either that it is not possible to effect complete removal of organic solvents from soils by aeration or heating or that organic solvents promote denitrification by solubilizing a fraction of soil organic matter that is not available to denitrifying microorganisms before the addition of these solvents. Experiments using phenylmercuric acetate (a herbicide and nitrification inhibitor) showed that although this compound had a marked inhibitory effect on denitrification when added to soil in methanol, ethanol, or acetone, it had no inhibitory effect on denitrification when added to soil in water. The work reported shows that the use of an organic solvent in adding an agricultural chemical to soil can lead to erroneous conclusions in studies on the effects of the chemical on soil denitrification.     

Nitrogen isotope discrimination in denitrification of nitrate in soils

Nitrogen isotope discrimination during denitrification in soils of nitrate containing natural concentrations of ¹⁴N and ¹⁵N was studied by determining the amount and the ¹⁵N content of nitrate-N and (nitrate + nitrite)-N in nitrate-treated soils incubated under anaerobic conditions (He atmosphere) for various times after treatment with glucose to promote denitrification. Analyses performed showed that the nitrate-N lost on incubation of these soils could largely be accounted for as products of denitrification (nitrite, NO. N₂O and N₂).The studies reported show that marked discrimination between ¹⁴N and ¹⁵N occurs during denitrification of nitrate in soils and that significant N isotope effects occur both in reduction of nitrate to nitrite and in reduction of nitrite to gaseous forms of N. They also indicate that the overall N isotope effect during denitrification of nitrate in soil will depend upon the tendency of the soil to accumulate nitrite under conditions that induce denitrification.It is concluded that discrimination between ¹⁴N and ¹⁵N during denitrification in soils of nitrate containing natural concentrations of these isotopes is of sufficient magnitude to invalidate the use of N isotope-ratio analyses for assessment of the contributions of soil and fertilizer N to nitrate in surface or ground waters or to nitrous oxide in the atmosphere.     

土壤氮气排放研究进展

自20世纪初人类发明并掌握工业合成氨的技术以来,氮肥施用量迅速增长。在一部分国家或地区,氮肥的施入量已经超过作物对氮素的需求,导致大量氮素损失到环境中,造成氨挥发、氧化亚氮排放、地下水硝酸盐污染等环境问题。土壤在微生物的作用下可以通过反硝化、厌氧氨氧化等过程将活性氮素转化为惰性氮气,达到清除过多活性氮的目的。由于大气中氮气背景浓度太高,因此很难直接准确测定土壤的氮气排放速率,导致土壤氮气排放通量、过程与调控机制研究远远落后于土壤氮循环的其他方面。本文综述了土壤氮气排放主要途径(反硝化、厌氧氨氧化与共反硝化)及其对土壤氮气排放的贡献;测定土壤氮气排放速率的方法(乙炔抑制法、氮同位素示踪法、N2/Ar比率-膜进样质谱法、氦环境法与N2O同位素自然丰度法)及其优缺点;调控土壤氮气排放通量的主要因素(氧气、可溶性有机碳、硝酸盐、微生物群落结构与功能基因表达等)及其相关作用机制。最后指出研发新的测定原位无扰动土壤氮气通量的方法是推进本领域相关研究的关键;定量典型生态系统(如旱地农田、稻田、森林、草地与湿地)土壤氮气排放通量,阐明其中的微生物学机制,模拟并预测土壤氮气排放对全球变化的响应规律是本领域的研究热点与发展方向。     

Modeling of Depleted Uranium Transport in Subsurface Systems

Groundwater and soil contamination with depleted uranium (DU) isan important public concern because of its long-term toxicity. In this study, the DU risk in groundwater was assessed through modeling of its sorption equilibrium and kinetics, as well as modeling of its transport in natural subsurface systems. Wheneverpossible, simulation results were compared with published experimental and field data. Equilibrium modeling studies showedthat DU sorption increased sharply from 0 to 100% in the pH range of 3.5 to 5.0 and maximum immobilization was established at pH > 5. Kinetic simulations indicated that the sorption of DUin subsurface systems is a rapid process. Simulations of DU mobility due to groundwater flow and due to infiltration, as wellas modeling of DU fate, were carried out by using a metal ion transport model, which included aqueous speciation, redox, precipitation, and sorption reactions. The results showed that the DU mobilization is a relatively slow process. Precipitation,redox, and sorption reactions resulted in the immobilization of DU. Among these reactions, sorption played a major role, and thepH of soils was critical in the immobilization; higher pH in soils resulted in greater immobilization of DU. The impact of DUtransport from infiltration was estimated based on four extremecases of climate and existing conditions of uranium penetrator fragments. The simulations demonstrated that the transport of DU in groundwater is slow due to the low infiltration rate and lowDU concentration resulted from the penetrators. Finally, modelingof DU fate showed that the natural cleanup of the DU-contaminatedsites is a slow process.     

Comparison of Five Adsorption Isotherms for Prediction of Zinc Retention in Calcareous Soils and the Relationship of their Coefficients with Soil Characteristics

Abstract

Zinc (Zn) deficiency is believed to be a consequence of reactions taking place between soluble Zn and the soil solid phase. This study was carried out to obtain quantitative relationships between Zn in equilibrium solution and that retained by the soil solids in calcareous soils. Twenty calcareous soils (saturated paste pH 6.9–7.9; calcium carbonate equivalent 4.64–22.80%) from Tehran province, Iran, were equilibrated with varying solution concentrations of Zn, and the amounts removed from the solution were used to check the fit to five adsorption isotherms, namely, Freundlich, Langmuir, Temkin, Gunary, and two‐surface Langmuir. Adsorption data of all soils showed statistically significant fit to the first four adsorption isotherms, but only 7 of the 20 soils tested showed fit to the two‐surface Langmuir. Coefficients of the adsorption isotherms showed statistically significant relationship with soil characteristics. Clay percentage, calcium carbonate equivalent percentage, and cation exchange capacity appeared to be the most influential soil characteristics with regard to Zn adsorption, whereas soil organic matter seemed to be of no importance under the conditions of this study.     

Copper Adsorption by Soils and its Relations with Plant Growth

Copper adsorption studies were conducted with 13 neutral to calcareous-alkaline soils. The data followed a Langmuir isotherm with two linear parts at low (part 1) and high (part 2) concentration of Cu in equilibrium solution. The ?pCu + 2pOH’? values show that part 1 and 2 stem largely from adsorption and precipitation reactions of Cu, respectively. The bonding energy and differential buffering capacity were significantly higher for part 1 while adsorption maximum and supply parameter were significantly higher for part 2 of the isotherms. Carbonate content, soil pH, organic matter, CEC and clay content were in that oder the predominant factors in elevating adsorption maximum, bonding energy coefficient and differential buffering capacity as well as decreasing supply parameter of soils. However, soil organic matter was the major determinant of strength of Cu adsorption. Copper potentials, adsorption maximum and differential buffering capacity were significantly correlated with dry matter production and Cu uptake in maize. The parameters of intensity factor predicted better the variation in yield and Cu uptake than the conventional soil test methods.     

Use of long-term monitoring data to derive a relationship between nitrogen surplus and nitrate leaching for grassland and arable land on well-drained sandy soils in the Netherlands

The decrease in nitrogen (N) use in agriculture led to improvement of upper groundwater quality in the Sand region of the Netherlands in the 1991–2009 period. However, still half of the farms exceeded the European nitrate standard for groundwater of 50 mg/l in the 2008–2011 period. To assure that farms will comply with the quality standard, an empirical model is used to derive environmentally sound N use standards for sandy soils for different crops and soil drainage conditions. Key parameters in this model are the nitrate-N leaching fractions (NLFs) for arable land and grassland on deep, well-drained sandy soils. NLFs quantify the fraction of the N surplus on the soil balance that leaches from the root zone to groundwater and this fraction represents N available for leaching and denitrification. The aim of this study was to develop a method for calculating these NLFs by using data from a random sample of commercial arable farms and dairy farms that were monitored in the 1991–2009 period. Only mean data per farm were available, which blocked a direct derivation of NLFs for unique combinations of crop type, soil type and natural soil drainage conditions. Results showed that N surplus leached almost completely from the root zone of arable land on the most vulnerable soils, that is, deep, well-drained sandy soils (95% confidence interval of NLF 0.80–0.99), while for grassland only half of the N surplus leached from the root zone of grassland (0.39–0.49). The NLF for grassland decreased with 0.015 units/year, which is postulated to be due to a decreased grazing and increased year-round housing of dairy cows. NLFs are positively correlated with precipitation surplus (0.05 units/100 mm for dairy farms and 0.10 units/100 mm for arable farms). Therefore, an increase in precipitation due to climate change may lead to an increase in leaching of nitrate.     

Biological Denitrification of Groundwater

Nitrate concentrations in groundwater have increased in many areas of the world. This causes serious concerns because of the link found between nitrate and the blue-baby syndrome, and of the possible formation of carcinogenic compounds in the digestive tract. Biological denitrification, bacteria-mediated reduction of nitrate to nitrogen gas, is a method used in the treatment of nitrate contaminated groundwater. The denitrifying microorganisms require carbon and energy substrates which may be organic or inorganic compounds. Treatment can take place in the aquifer (in situ treatment) or in above ground reactors. Numerous biological denitrification processes have been reported; this paper reviews some of this work and studies in progress in the author's laboratory. The choice of a biological denitrification system has to be considered on an individual basis. Although preventive measures are curbing the problem in some developed countries, nitrate pollution is still on the rise in many other countries. Innovative, low-cost biological denitrification processes are specially needed in developing countries.     

EVALUATION OF POTENTIAL SUBSTRATES TO MONITOR RESPIRATORY NITRATE REDUCTASE ACTIVITY IN SOILS

Different inorganic ions were tested for their ability to replace nitrate as the terminal oxidant for bacterial respiration in anaerobic soils. Chlorate, bromate. selenate. tellurite and ferric ions were all unsuitable substitutes, lodate reduction in soils was similar to nitrate reduction because it required anaerobic conditions, was increased by glucose amendment and decreased by phenylmercuric acetate. Amendment of soils with iodate and measurement of iodide production can be used to measure nitrate reductase activity in a soil and so give a qualitative indication, and possibly a quantitative estimate, of the denitrification capacity of soils.     

Acetochlor as a soil pollutant

The agricultural use of pesticides leads to diffuse pollution whereby the various contaminants of the soil infiltrate into the groundwater reaching lakes and drinking water aquifers. Due to the extensive application of these chemicals, their leaching presents a high environmental risk. Since the adsorption coefficient (K) characterizes the soil / water partitioning [1] and is also representative for leaching, the first step in understanding of the environmental fate of a pollutant is to study its adsorption properties. Weak binding to the soil constituents (low K) leads to groundwater pollution, while a strong binding (high K) results in surface water pollution through the erosion of the soil. Acetochlor is a widely used herbicide all over the world. Similar to other organic pollutants, the environmental fate of this chemical is strongly related to its adsorption properties. Static adsorption equilibrium measurements were carried out at 25°C on different types of Hungarian soils (chernozem, brown forest and sandy soil) characterized by varying amounts of organic matter and pH values. Acetochlor solutions were prepared in the presence of nitrate and phosphate ions (0.1 mol/L sodium nitrate and 0.1 mol/L phosphate uffer, pH=7) which are constituents of fertilizers occurring in high concentrations in the environment. In order to appreciate their effect, adsorption studies were also performed in pure aqueous medium. The equilibrated liquid was analyzed after centrifugation by two different methods (Total Organic Carbon measurement, High Performance Liquid Chromatography). Isotherms obtained under different conditions, as well as on various soils, exhibit a similar shape, thus indicating a two-step adsorption process. The plots cannot be interpreted according to the classes of isotherms suggested by Giles (H-, L- and C-type, [2]). The adsorption coefficients were estimated from the initial slope of the curves. These values were determined not only by the type of the soil, but also by the composition of the aqueous media. Due to the low value of the adsorption coefficients, the acetochlor is a rather mobile pollutant of the soil posing a potential danger to the aquatic environment. The organic matter adsorption coefficients (K_om) [3] were also calculated and they were approximately identical for soils of high organic matter. For the chernozem and brown forest soils, the values of the K and K_om parameters are increasing in the order from water < phosphate buffer < sodium nitrate. For soils of low organic content, the similarity of the K_om values cannot be expected (due to the hyperbolic nature of the equation) as the data really indicate it for the adsorption behavior of the sandy soil. Here, the organic matter plays a less important role and the adsorption is controlled by the solute / inorganic substance interactions. This conclusion is nicely proved by the adsorption of the acetochlor on quartz resulting thereby in a similar plot being obtained for the soils. According to the hypothesis presented here, the first step of the isotherms is controlled by the solute / surface interactions while the solute / adsorbed solute interactions are operating in the second step of the isotherm. The role of the organic matter in this region of the isotherm is probably negligible. The comparison of the adsorption coefficients leads to the conclusion that the presence of nitrate and phosphate ions enhances the adsorption of acetochlor on the soils containing a high percentage of organic matter. As these ions are present in the environment due to the extensive use of fertilizers, they may increase the acetochlor pollution of water by erosion. This conclusion corroborates those earlier observations that reported frequent acetochlor contamination of the surface waters [4–5]. As the organic matter content of the soils plays an important role in the acetochlor adsorption, humic substances must have a strong influence on the transport of this compound. Experiments to obtain adsorption isotherms of further pesticides and the development of a quantitative model are in progress.     

Participation of soluble and oxidizable soil organic compounds in denitrification

Summary The role of soluble organic carbon (SOC) in denitrification in four mineral soils and one organic soil was evaluated in laboratory studies. Denitrification capacities and SOC concentrations were determined by nitrate loss from air-dried flooded soil treated with a solution containing 100 g/ml N0₃ ^–-N, while the rate of consumption was measured by Warburg manometry on 20 g air-dried soils to which 10 ml water had been added. High correlation coefficients (r > 0.93) were obtained between denitrification capacities, SOC, and oxygen consumption in the five soils. A mineral soil was amended with extracts of an organic soil. After incubating for 1 week, denitrification capacity was enhanced and SOC concentrations decreased in that soil. Extracted mineral soil had a lower denitrification capacity than an unextracted one. Decreases in concentrations of SOC were related to color change. Infrared spectra of precipitates from soil extracts indicated that absorption at wave number 1420–1440 cm -1 was also related to the color changes. It was implied that low molecular weight fulvic acid like compounds represented the SOC mineralized in denitrification, and that their supply to soil solution by solubilization of organic matter influenced the denitrification rate in the soil.     

Availability of organic carbon for denitrification of nitrate in subsoils

Summary Previous work in our laboratory indicated that the slow rate of denitrification in Iowa subsoils is not due to a lack of denitrifying microorganisms, but to a lack of organic C that can be utilized by these microorganisms for reduction of NO ₃ ^– . This conclusion was supported by studies showing that drainage water from tile drains under agricultural research plots contained only trace amounts of organic C and had very little, if any, effect on denitrification in subsoils. Aqueous extracts of surface soils promoted denitrification when added to subsoils, and their ability to do so increased with increase in their organic C content. Amendment of surface soils with corn and soybean residues initially led to a marked increase in the amounts of organic C in aqueous extracts of these soils and in the ability of these extracts to promote denitrification in subsoils, but these effects were short-lived and could not be detected after incubation of residue-treated soils for a few days. We conclude from these observations that water-soluble organic C derived from plant residues is decomposed so rapidly in surface soils that very little of this C is leached into subsoils, and that this largely accounts for the slow rate of denitrification of nitrate in subsoils.