综合化学法和生物标记物法评价土壤中豆磺隆的生物有效性

Bioavailability is a critical factor for assessing the environmental risk of organic pollutants in soil. In this study, extractions with 3 different solvents, including 2 aqueous solutions, calcium chloride (CaCl₂) and a phosphate buffer solution (PBS), and a mixture of aqueous solution and organic solvent, a PBS-methanol (8:2, volume/volume) mixture (PBS-M), were performed to assess the bioavailability of chlorimuron-ethyl in soil in comparison to a battery of toxicity tests in wheat seedlings. The results indicated that the peroxidase (POD) activity in wheat leaves after 7 d of exposure was one of the sensitive biomarkers of chlorimuron-ethyl in soil. The extractability of chlorimuron-ethyl by all the 3 solvents decreased with exposure time, and the rate of decrease of the PBS-M extraction between 1 and 7 d of exposure was substantially higher than those of the aqueous solution extractions. Chlorimuron-ethyl gradually changed from a water-soluble form into a soil organic matter (SOM)-bound form in the soil. The PBS extraction correlated best with the POD activity in the leaves after 7 d of exposure.     

Extraction of water‐soluble organic matter from mineral horizons of forest soils

Dissolved organic matter (DOM) is involved in many important biogeochemical processes in soil. As its collection is laborious, very often water‐soluble organic matter (WSOM) obtained by extracting organic or mineral soil horizons with a dilute salt solution has been used as a substitute of DOM. We extracted WSOM (measured as water‐soluble organic C, WSOC) from seven mineral horizons of three forest soils from North‐Rhine Westphalia, Germany, with demineralized H₂O, 0.01 M CaCl₂, and 0.5 M K₂SO₄. We investigated the quantitative and qualitative effects of the extractants on WSOM and compared it with DOM collected with ceramic suction cups from the same horizons. The amounts of WSOC extracted differed significantly between both the extractants and the horizons. With two exceptions, K₂SO₄ extracted the largest amounts of WSOC (up to 126 mg C kg^–1) followed by H₂O followed by CaCl₂. The H₂O extracts revealed by far the highest molar UV absorptivities at 254 nm (up to 5834 L mol^–1 cm^–1) compared to the salt solutions which is attributed to solubilization of highly aromatic compounds. The amounts of WSOC extracted did not depend on the amounts of Fe and Al oxides as well as on soil organic C and pH. Water‐soluble organic matter extracted by K₂SO₄ bore the largest similarity to DOM due to relatively analogue molar absorptivities. Therefore, we recommend to use this extractant when trying to obtain a substitute for DOM, but as WSOM extraction is a rate‐limited process, the suitability of extraction procedures to obtain a surrogate of DOM remains ambiguous.     

Kinetics of the release of dissolved organic matter (DOM) from air‐dried and pre‐moistened soil material

In this study, the kinetics of soil organic matter (SOM) dissolution from soil samples in different states of moisture was investigated, using a continuous extraction method. The investigation distinguished three processes of SOM dissolution. They include an initial, fast process (probably hydrophilic dissolved organic matter) and two slow, rate limited processes, which probably correspond to hydrophobic dissolved organic matter (DOM). The second process indicates a slow, continuous release of DOM, whereas the third process is determined by a power law. The rate of the third process strongly depends on temperature and state of moisture. It is diffusion limited, with the diffusion control probably being located in the solid soil organic matter. This was explained by a gel structure, which slowly forms in the hydrating SOM and allows diffusion of mobile particles of SOM. The results show the importance of considering the moisture state of SOM for the kinetics of DOM dissolution.     

A comparison of different indices for nitrogen mineralization

Indices of N mineralization in soils of contrasting texture, pH, and organic matter contents were compared at different dates during the growing season. The indices were derived from a 12-week aerobic incubation, determination of the amount of microbial biomass at the start of the incubation, determination of the increase in NH ₄ ⁺ after boiling with 2 M KCl for 2h, and extraction of total soluble N with 0.01 M CaCl₂. Cumulative mineral N increased linearly with time in the course of the incubations. Rates of mineralization in soil samples taken in March 1989 and 1990 were significantly correlated with soluble organic N, while correlations between the mineralization rate and the increase in NH ₄ ⁺ after boiling with 2 M KCl for 2 h were poor for sandy soils and absent for loamy soils. Correlations between NH ₄ ⁺ after boiling with 2 M KCl for 2h and the soil N concentration were highly significant, but no general relationship was found between the mineralization rate and the soil N concentration. Neither biomass N nor biomass C was significantly correlated with the mineralization rate or with one of the chemical indices. Among the methods tested, soluble organic N extracted with 0.01 M CaCl₂ was the only method with any promise for routine measurement of the mineralization capacity of the individual sites.     

Molybdenum Determination in Mehlich‐1 and Mehlich‐3 Soil Test Extracts and Molybdenum Adsorption in Brazilian Soils

Abstract

The extractant Mehlich‐1 is routinely used in Brazil for determination of soil nutrients, whereas Mehlich‐3 has been suggested as a promising extractor for soil fertility evaluation. Both were used for extraction of molybdenum (Mo) in Brazilian soils with Mo dosage by the KI+H₂O₂ method. The Langmuir and Freundlich isotherms were used to study soil Mo adsorption. Mehlich‐1 extracted more Mo than Mehlich‐3 in soils with high contents of organic matter, clay, and iron (Fe) oxides. Mehlich‐3 and Mehlich‐1 extractions correlated positively and significantly with amorphous Fe oxides, crystalline Fe oxides, and organic matter. Molybdenum recovering rates correlated to crystalline Fe oxides and clay contents but not to organic matter, pH, and Mo adsorption capacity. Amorphous and crystalline Fe oxides, clay, and organic matter were responsible for most of the Mo adsorption. The Langmuir isotherm described better the Mo adsorption to soil amorphous Fe oxides and organic matter than the Freundlich isotherm.     

Humification-mineralization pyrolytic indices and carbon fractions of soil under organic and conventional management in central Italy

The aim of this study was to evaluate chemical changes in soil organic matter (SOM) in organically and conventionally managed fields, using pyrolytic indices and the extraction of different carbon fractions. Pyrolysis-gas chromatography (Py-GC) was used to study structural changes in SOM, whereas the different soil extractions gave a fractionation of C forms. Organic management increased both humic and labile C forms (microbial biomass C and water soluble organic C). A significant positive relationship was found between the living SOM fraction, expressed as microbial biomass/total organic C ratio (MBC/TOC) and humification rate. A negative relationship was found between the pyrrole to phenol ratio (O/Y) and total extractable C (TEC).An opposite trend has been observed for the second pyrolytic index (N/O), which represents the mineralization of fresh organic matter. Mineralization was higher in organically managed soil, probably because of consistent input of fresh material to the organic field. Carbon fraction pools and pyrolytic indices provided complementary indications of SOM quality under organic and conventional management.     

长期不同施肥条件下黑土的有机质含量变化特征

以吉林公主岭黑土有机肥化肥配施30年长期定位试验结果为材料,分析了长期不同施肥下黑土有机质的变化特征。结果表明,长期不施肥或单施化肥(M0区)土壤有机质含量呈下降趋势,30年下降幅度为2.1%～7.9%;施用常量有机肥(M2区)和高量有机肥(M4区)的土壤有机质含量呈增加趋势,30年M2区和M4区有机质累积增加幅度分别为42.2%～50.0%和81.5%～94.7%。M2区和M4区有机质增加幅度因施用有机肥中有机质含量的变化可分为两个阶段,1980～1992年增加幅度分别平均为2.4%和9.3%,12年后随着有机肥中有机质含量增加,后18年M2区和M4区有机质累积增加幅度分别平均为41.4%和71.5%。施用相同化肥条件下配施不同水平有机肥,各处理间土壤有机质含量差异达到显著水平;而在施用相同有机肥条件下配施不同化肥时,各处理间有机质含量差异不显著。由此可以得出,有机肥的数量和有机质含量是影响土壤有机质含量变化的主要因素,因此,选择合适的有机肥数量和有机质含量是提升土壤有机质的主要措施,在东北黑土上施用优质高量有机肥可迅速提高土壤有机质含量。     

Applicability of 0.01 M CaCl2 as a single extraction solution for the assessment of the nutrient status of soils and other diagnostic purposes

Abstract

The applicability of 0.01 M CaCl₂ solution as a single extraction agent for soils as a basis for fertilizer recommendation was tested on a variety of soils both from the Netherlands and from some tropical countries. Air‐dry soil samples were subjected to extraction with 0.01 M CaCl₂ and to several conventional extraction procedures, and the results were compared. In the soil suspensions pH was measured, whereas in the extracts Na, K, Mg, P, different extractable N‐forms and Zn were measured. The values found in CaCl₂ extracts are discussed in relation to results of other extraction procedures and as to their potential value in soil quality assessment. It is concluded that a single extraction procedure with 0.01 M CaCl₂ can be applied for fertilizer recommendation purposes. The possibility of determining different extractable N‐forms (NH₄, NO₃, soluble organic N) significantly enhances the value of the method in predicting the N‐fertilizer needs. Furthermore it was found that the concentration of Zn in 0.01 M CaCl₂ extracts was a good indicator of phytotoxicity in a polluted area. Additional advantages of this extraction are low costs, simplicity and repro‐ducibility.     

Relating the biological stability of soil organic matter to energy availability in deep tropical soil profiles

Tropical subsoils contain large reservoirs of carbon (C), most of which is stored in soil organic matter (SOM). Subsoil OM is thought to be particularly stable against microbial decomposition due to various mechanisms and its position in the soil profile, potentially representing a long-term C sink. However, few experiments have explicitly investigated SOM stability and microbial activity across several orders of magnitude of soil C concentrations as a function of soil depth. The objective of this study was to evaluate the biological stability of SOM in the upper 1.4 m of tropical forest soil profiles. We did so by measuring CO₂ evolution during a 90-day laboratory incubation experiment on a sample set that was previously characterized for C and nutrient concentrations and microbial biomass. We concurrently measured the energy content of SOM using differential scanning calorimetry (DSC) as an index of the energy available for microbial metabolism, with the hypothesis that the biological stability of SOM would be inversely related to the energy contained within it. Cumulative CO₂ evolution, mean respiration rates, and the energy density of SOM (energy released during combustion normalized to soil C) all declined with soil depth (P < 0.01). Biological indices of C stability were well correlated with measures of SOM energy. There was no change in the mean respiration rate as a function of depth when normalized to soil C, and a trend toward increased respiration per-unit microbial biomass (P = 0.07). While reduced microbial respiration in subsoils suggests an increase in the biological stability of SOM, we suggest this is driven principally by concurrent declines in energy availability as measured by DSC and the size of the microbial biomass pool. On a per-unit biomass basis, subsoil OM may be as prone to decomposition and destabilization as surface SOM.     

Structural changes in humic substances after long-term fertilization of a calcareous soil with pig slurries

Pig slurries are widely used on calcareous soils in European rainfed systems. Here we assess their impact on the amount of soil organic carbon (SOC) and on the composition of humic-type substances (HTS). Seven doses of slurry (five from fattening pigs and two from sows) ranging from 1.0 to 4.8 Mg ha⁻¹ yr⁻¹ of organic matter were evaluated after a period of 12 years and compared with mineral fertilizer treatment. At the end of the last annual cropping season (September), SOC was quantified, and HTS were isolated by alkaline extraction followed by acid precipitation, and studied by visible spectroscopy (800–400 nm) and Fourier-transformed infrared spectroscopy (4000–400 cm⁻¹). Following the trend in the slurry organic matter applied rates, SOC increased from 9.5 g C kg⁻¹ (mineral treatment) to 13.8 g C kg⁻¹. This SOC increase was equivalent to c. 25.4% of the slurry organic carbon applied. The incorporation of aliphatic structures, mainly polyalkyl, from slurries into the HTS tends to modify the composition of the soil organic matter (SOM), which is reflected in a decrease in the intensity of FT-IR peaks related to aromatic structures. Despite the trend of significant increase in SOC with fattening slurries, mainly from the organic matter rate of 1.6 Mg ha⁻¹ yr⁻¹ (c. 185 kg N ha⁻¹), the composition of the HTS showed an important aliphatic enhancement. The FTIR results showed that using exclusively the relative intensities of specific peaks (alkyl, carboxyl, aromatic and amide groups) as variables for the discriminant analysis, it is possible to identify HA between different groups of soils treated with progressive levels of slurry. Although the new aliphatic components could be considered important to improve soil physical quality, after the incorporation of additional SOM, the spectroscopic characteristics of HTS in soils treated with slurries suggested a weak effect in long-term C sequestration, as the newly incorporated OC forms are not qualitatively similar to the presumably stable native SOM. These potential changes in SOC and SOM composition at field level are constrained by the maximum allowed N rates from organic origin in some agricultural systems.     

Relationship Between Soil Properties and Nitrogen Mineralization in Undisturbed Soil Cores from California Agroecosystems

Soil nitrogen (N) mineralization rates from different agricultural regions in California were determined and related to soil properties. Undisturbed soil cores were sampled in spring from 57 fields under annual crop rotations and incubated at 25℃ for 10 weeks. Soil properties varied across and within regions, most notably those related to soil organic matter (SOM), with total soil carbon ranging from 6 to 198 g kg^?1. Multivariate linear regression was used to select soil properties that best predicted N mineralization rates. Regression models with a good fit differed between soils with high and low SOM contents, but generally included a measure of SOM quantity, its quality as well as soil texture or mineralogy. Adjusted R² values were 0.95 and 0.60 for high and low SOM soils, respectively. This study has shown that information on soil properties can contribute to better estimates of N mineralization in soils of contrasting characteristics.     

Comparison of Chemical Methods of Assessing Potentially Available Organic Nitrogen from Organic Residues Applied to a Sandy Soil

Abstract

More than 90% of the nitrogen (N) in soils is bond as organic N compounds. The available N can be estimated on the mineral N released during time‐consuming incubations of soil. Several chemical methods have been developed as substitutes for incubations. On the other hand, there has been an increase in waste production. Residues could potentially offset the need for mineral fertilizers, being both an economic and environmental benefit. Thus, the development of a routine method for prediction of N supply both from soil organic matter (SOM) and the application of organic residues is of great interest. An incubation experiment was performed in a Cambic Arenosol to evaluate different chemical methods. Air‐dried soil was mixed with increasing amounts of composted solid municipal waste, secondary pulp‐mill sludge, hornmeal, poultry manure, the solid phase from pig slurry, and composted pig manure. Samples were incubated for 244 days under a controlled environment. Among the chemical extractants studied, hot 2 M potassium chloride (KCl) and hot 0.01 M calcium chloride (CaCl₂) showed promise in indicating values of N₀ (potentially available nitrogen), and these simple methods are suitable for use in routine laboratory conditions.     

Loss of low molecular weight dissolved organic carbon (DOC) and nitrogen (DON) in H2O and 0.5 M K2SO4 soil extracts

Soil extracts are routinely used to quantify dissolved organic nutrient concentrations in soil. Here we studied the loss and transformation of low molecular weight (LMW) components of DOC (¹⁴C-glucose, 1 and 100 μM) and DON (¹⁴C-amino acid mixture, 1 and 100 μM) during extraction of soil (0-6 h) with either distilled water or 0.5 M K₂SO₄. The extractions were performed at 20 °C, at 4 °C, or in the presence of an inhibitor of microbial activity (HgCl₂ and Na-azide). We showed that both glucose and amino acids became progressively lost from solution with increasing shaking time. The greatest loss was observed in H₂O extracts at 1 μM for both substances (>90% loss after 15 min). Lower temperature (4 °C) and presence of K₂SO₄ both resulted in reduced loss rates. The presence of microbial inhibitors effectively eliminated the loss of glucose and amino acids. We conclude that microbial transformation of LMW-DOC and DON during H₂O or K₂SO₄ extraction of soil may affect the estimation of their concentrations in soil. This finding has significant implications for methods that rely on chemical extractions to estimate LMW-C components of DOC and DON.     

Extractability of labelled microbial biomass N by electro-ultrafiltration and CaCl2 extraction

A laboratory soil incubation and a pot experiment with ryegrass were carried out in order to examine the extractability of microbial biomass N by using either 10-mM CaCl₂ extraction or the electro-ultrafiltration (EUF) method. The aim of the experiment was to test the hypothesis whether the organic N (Norg) extracted by EUF or CaCl₂ from dried soil samples represents a part of the microbial biomass. For the laboratory incubation a ¹⁵N-labelled Escherichia coli suspension was mixed with the soil. For the pot experiment a suspension of ¹⁵N-labelled bacteria was applied which had previously been isolated from the soil used. Soil samples of both treatments, with and without applied bacterial suspension, were extracted by EUF and CaCl₂. The extractability of applied microbial biomass was estimated from the difference in extractable Norg between the two treatments. In addition, the N isotopic composition in the upper plant matter, in the soil, and in organic and inorganic N fractions of EUF and CaCl₂ extracts was analysed. Both experiments showed that the applied microbial biomass was highly accessible to mineralization and thus represented potentially mineralizable N. However, this mineralizable N was not extractable by CaCl₂ or by the EUF method. It was, therefore, concluded that the organic N released on soil drying and which was thus extractable was derived from the non-biomass soil organic matter. The result suggests that both extraction methods may provide a suitable index for mineralizable N only in cases where the decomposable organic substrates are derived mainly from sources other than the living soil biota.Dedicated to Professor J. C. G. Ottow on the occasion of his 60th birthday     

从高山火山灰中提取铝, 铁和有机碳的可供选择的方法

Montane volcanic ash soils contain disproportionate amounts of soil organic carbon and thereby play an often underestimated role in the global carbon cycle.Given the central role of Al and Fe in stabilizing organic matter in volcanic ash soils,we assessed various extraction methods of Al,Fe,and C fractions from montane volcanic ash soils in northern Ecuador,aiming at elucidating the role of Al and Fe in stabilizing soil organic matter(SOM).We found extractions with cold sodium hydroxide,ammonium oxalate/oxalic acid,sodium pyrophosphate,and sodium tetraborate to be particularly useful.Combination of these methods yielded information about the role of the mineral phase in stabilizing organic matter and the differences in type and degree of complexation of organic matter with Al and Fe in the various horizons and soil profiles.Sodium tetraborate extraction proved the only soft extraction method that yielded simultaneous information about the Al,Fe,and C fractions extracted.It also appeared to differentiate between SOM fractions of different stability.The fractions of copper chloride-and potassium chloride-extractable Al were useful in assessing the total reactive and toxic Al fractions,respectively.The classical subdivision of organic matter into humic acids,fulvic acids,and humin added little useful information.The use of fulvic acids as a proxy for mobile organic matter as done in several model-based approaches seems invalid in the soils studied.     

Untargeted soil metabolomics methods for analysis of extractable organic matter

The cycling of soil organic matter (SOM) by microorganisms is a critical component of the global carbon cycle but remains poorly understood. There is an emerging view that much of SOM, and especially the dissolved fraction (DOM), is composed of small molecules of plant and microbial origin resulting from lysed cells and released metabolites. Unfortunately, little is known about the small molecule composition of soils and how these molecules are cycled (by microbes or plants or by adsorption to mineral surfaces). The water-extractable organic matter (WEOM) fraction is of particular interest given that this is presumably the most biologically-accessible component of SOM. Here we describe the development of a simple soil metabolomics workflow and a novel spike recovery approach using ¹³C bacterial lysates to assess the types of metabolites remaining in the WEOM fraction. Soil samples were extracted with multiple mass spectrometry-compatible extraction buffers (water, 10 mM K₂SO₄ or NH₄HCO₃, 10–100% methanol or isopropanol/methanol/water [3:3:2 v/v/v]) with and without prior chloroform vapor fumigation. Profiling of derivatized extracts was performed using gas chromatography/mass spectrometry (GC/MS) with 55 metabolites identified by comparing fragmentation patterns and retention times with authentic standards. As expected, fumigation, which is thought to lyse microbial cells, significantly increased the range and abundance of metabolites relative to unfumigated samples. To assess the types of microbial metabolites from lysed bacterial cells that remain in the WEOM fraction, an extract was prepared from the soil bacterium Pseudomonas stutzerii RCH2 grown on ¹³C acetate. This approach produced highly labeled metabolites that were easily discriminated from the endogenous soil metabolites. Comparing the composition of the fresh bacterial extract with what was recovered following a 15 min incubation with soil revealed that only 27% of the metabolites showed >50% recovery in the WEOM. Many, especially cations (polyamines) and anions, showed <10% recovery. These represent metabolites that may be inaccessible to microbes in this environment and would be most likely to accumulate as SOM presumably due to binding with minerals and negatively-charged clay particles. This study presents a simple untargeted metabolomics workflow for extractable organic matter and an approach to estimate microbial metabolite availability in soils. These methods can be used to further our understanding of SOM and DOM composition and examine the link between metabolic pathways and microbial communities to terrestrial carbon cycling.     

黄淮海平原集约种植条件下土壤有机质动态模拟

A modified CQESTR model, a simple yet useful model frequently used for estimating carbon sequestration in agricultural soils, was developed and applied to evaluate the effects of intensive cropping on soil organic matter （SOM） dynamics and mineralization as well as to estimate carbon dioxide emission from agricultural soils at seven sites on the Huang-Huai-Hai Plain of China. The model was modified using site-specific parameters from short- and mid-term buried organic material experiments at four stages of biomass decomposition. The predicted SOM results were validated using independent data from seven long-term （10- to 20-year） soil fertility experiments in this region. Regression analysis on 1 151 pairs of predicted and measured SOM data had an r2 of 0.91 （P≤0.01）. Therefore, the modified model was able to predict the mineralization of crop residues, organic amendments, and native SOM. Linear regression also showed that SOM mineralization rate （MR） in the plow layer increased by 0.22% when annual crop yield increased by 1 t ha^-1 （P ≤ 0.01）, suggesting an improvement in SOM quality. Apparently, not only did the annual soil respiration efftux merely reflect the intensity of soil organism and plant metabolism, but also the SOM MR in the plow layer. These results suggested that the modified model was simple yet valuable in predicting SOM trends at a single agricultural field and could be a powerful tool for estimating C-storage potential and reconstructing C storage on the Huang-Huai-Hai Plain of China.     

Estimation of turnover and equilibrium of soil organic matter using a mathematical approach

The methods based on N uptake of aerial-plants, soil organic matter （SOM） dynamics, Jenny＇s equation, and actual measurement of long-term field experiments in Jiaxing, Quzhou, Huangyan and Hangzhou of Zhejiang Province, China were used to determine the organic mineralization rate being helpful in estimating the organic requirement for SOM equilibrium. The results showed that the estimated mineralization ratios of SOM for Jiaxing and Quzhou were, respectively, 0.0404 and 0.0508 based on N uptake of aerial-plants in non-fertilized plots; 0.0405 and 0.012 using SOM dynamics in non-fertilized plots; and 0.0413 and 0.0513 using the actual investigated data and Jenny＇s equation. With Jenny＇s equation, soil organic C balance in manure ＋ N-P-K plots was estimated at nearly 28.8 g kg^-1 for Jiaxing and 32.4 g kg^-1 for Quzhou with predicted SOM linearly related to the actual investigated values （r^2 = 0.9640 for Jiaxing and 0.8541 for Quzhou）. To maintain the SOM balance in the non-fertilized plots the recommended rate of organic materials was 3 000-6 600 kg ha^-1, and the relevant rates of farm yard manure （FYM） in the manure and N-P-K plots were estimated at 3 375 （dry） and 17670 kg ha^-1 （wet） for Jiaxing, 1845 （dry） and 6090 kg ha^-1 （wet） for Quzhou.     

Differences in the Influence of Cadmium on the Decomposition of Various Types of Organic Materials in Soil

The influence of Cd on the decomposition of various types of organic materials in soil was studied. CdCl₂ or CaCl₂ (control) was added to a Gley soil at a level of 10 mmol kg^-1 soil. Three days later, organic materials including glutamic acid, glucose, casein, starch, cellulose, lignin, rice straw, rice straw compost, or 3 kinds of sludges were mixed with the soil in a proportion of 1%, respectively. During an 8-week period of incubation at 28°C, CO₂ evolution was measured periodically. At the end of the incubation period, the form of Cd in the soil was analyzed by successive extractions with water, CaCl₂, CH₃COOH, Na₄P₂O₇, and with hot HCl after HNO₃-HClO₄ digestion.

The decomposition of all the organic materials was inhibited by the addition of Cd, but the degree of inhibition varied considerably among the types of organic materials. The decomposition of rice straw, rice straw compost, and sludges was markedly inhibited by Cd. The amount of water-soluble Cd was less in the soils treated with rice straw, rice straw compost, and sludges than in the soils treated with other types of organic materials, while the amounts of CaCI₂-extractable Cd were much larger in the latter soils. In the case of rice straw, rice straw compost, and sludges Cd was easily adsorbed from the CdCl₂ solution.

These results suggest that the inhibition of organic matter decomposition by Cd is caused by the adsorption of Cd onto organic matter.     

Changes in soil pH and phosphorus availability during decomposition of cover crop residues

The aim of this study was to determine the effect of winter cover crop (CC) residues on soil pH and phosphorus (P) availability. Three incubation assays were performed in pots using two CC: vetch (V) (Vicia villosa Roth.) and oats (Oa) (Avena sativa L.). Soil samples were taken from 10 sites at 0–20-cm depth. The rate of residues were 0 (D0), 10 (D1), 20 (D2), 30 (D3), and 40 (D4) g dry matter kg^?1 soil and the soil sampling was after 10, 20, 30, 60, 90, and 120 days of incubation. Soil pH, extractable P (Pe), and soil organic matter (SOM) and its fractions were determined. The pH increase was correlated with the rate applied (D1 < D2 < D3 < D4). No differences were found for pH comparing V and Oa residues with low residue rates. Soil pH changes were dependent from initial pH and SOM fractions in different soils across the incubation period. The multiple regression models showed that the pH changes were dependent on initial pH level and SOM fractions with a high R² (0.81). CC residues and its quantities produced different changes on pH – especially at the beginning of the incubation – which influenced the P availability.