The influence of tillage systems on soil organic matter and soil hydrophobicity

Management practices including various tillage systems influence quantity and composition of soil organic matter (SOM). Parameters for evaluating both the SOM quantity (organic C [C_ox], total N [N_t]) and quality (microbial biomass C, hydrophobic and hydrophilic organic components) were determined in soil samples, taken from two soil depths (0–0.1 m and 0.1–0.3 m) in a field experiment in the period 2001–2007, with different tillage systems. The experiment, founded in 1995 in Prague-Ruzyně, includes conventional soil tillage (CT) plus some selected methods of conservation tillage: (a) no tillage (NT), (b) no tillage + mulch (NTM), and (c) minimum tillage with pre-crop residues incorporated (MTS). C_ox and microbial biomass C contents increased significantly with conservation tillage as compared to CT in 0–0.1 m layer, non-significant increase was found in 0.1–0.3 m layer. N_t increased non-significantly in both layers. Along with the depth of sampling, the content of the characterized parameters decreased in all variants; but the decrease in the conventionally tilled variant was, for the most part, lower than in the conservation tillage. The functional hydrophobic and hydrophilic groups of soil organic matter were identified by Fourier transform infrared (FTIR) spectroscopy, and the hydrophobic/hydrophilic group intensities ratio was calculated as the parameter of soil hydrophobicity. A higher soil hydrophobicity existed in all three conservation tillage treatments compared to CT due to the significantly higher content of hydrophobic organic components. C_ox correlated significantly with microbial biomass C, N_t, hydrophobic components, and soil hydrophobicity (R = 0.552–0.654; P < 0.05). Hydrophilic components did not correlate with other soil characteristics, with the exception of hydrophobic components. These data show that shifting from CT to the conservation tillage systems increased the content of SOM in top soil layer in relatively short time, improved the SOM quality and increased soil hydrophobicity in the condition of experiment.     

Managing soil organic matter – implications for soil structure on organic farms

Abstract. This paper reviews current understanding of soil structure, the role of soil organic matter (SOM) in soil structure and evidence for or against better soil physical condition under organic farming. It also includes new data from farm case studies in the UK. Young SOM is especially important for soil structural development, improving ephemeral stability through fungal hyphae, extracellular polysaccharides, etc. Thus, to achieve aggregate stability and the advantages that this conveys, frequent input of fresh organic matter is required. Practices that add organic material are routinely a feature of organically farmed soils and the literature generally shows that, comparing like with like, organic farms had at least as good and sometimes better soil structure than conventionally managed farms. Our case studies confirmed this. In the reviewed papers, SOM was generally larger on the biodynamic/organic farms because of the organic additions and/or leys in the rotation. We can therefore hypothesize that, because it is especially the light fraction of SOM that is involved in soil structural development, soil structure will improve in a soil to which fresh organic residues are added regularly. Thus, we argue it is not the farming system per se that is important in promoting better physical condition, but the amount and quality of organic matter returned to a soil.     

Water-extractable soil carbon in relation to the belowground carbon cycle

We investigated the role of water-extractable carbon (C-extr) as potential substrate for forest soil microorganisms by comparing belowground C fluxes at a plot with the forest floor removed (no-litter) and at a control plot. One-third lower soil respiration rates at the no-litter plot gave evidence that the forest floor was the source of considerable amounts of microbially degradable C. Laboratory incubation of C-extr, fractionated into neutral and acid moieties, showed that part of the C-extr was degraded rapidly, and that the high-molecular-weight acid fraction was much less degradable than the neutral C. To the extent that the degradable portion of the water-extractable C can be regenerated quickly, it may supply much of the substrate for heterotrophic soil respiration. Received: 11 December 1995     

Microbial community structure and characteristics of the organic matter in soils under Pinus sylvestris, Picea abies and Betula pendula at two forest sites

 Microbial biomass C (C_mic), C mineralization rate, phospholipid fatty acid (PLFA) profiles and community level physiological profiles (CLPPs) using Biolog were determined from the humus and mineral soil layers in adjacent stands of Scots pine (Pinus sylvestris L.), Norway spruce [Picea abies (L.) Karst.] and silver birch (Betula pendula Roth) at two forest sites of different fertility. In addition, the Fourier-transformed infrared (FTIR) spectra were run on the samples for characterization of the organic matter. C_mic and C mineralization rate tended to be lowest under spruce and highest under birch, at the fertile site in all soil layers and at the less fertile site in the humus layer. There were also differences in microbial community structure in soils under different tree species. In the humus layer the PLFAs separated all tree species and in the mineral soil spruce was distinct from pine and birch. CLPPs did not distinguish microbial communities from the different tree species. The FTIR spectra did not separate the tree species, but clearly separated the two sites. Received: 3 December 1999     

Exploring soil microbial communities and soil organic matter: Variability and interactions in arable soils under minimum tillage practice

This study describes an integrated approach (1) to monitor the quantity and quality of water extractable organic matter (WEOM) and size, structure and function of microbial communities in space (depth) and time, and (2) to explore the relationships among the measured properties. The study site was an arable field in Southern Germany under integrated farming management including reduced tillage. Samples of this Eutric Cambisol soil were taken in July 2001, October 2001, April 2002 and July 2002 and separated into three depths according to the soil profile (0–10 cm, 10–28 cm and 28–40 cm). For each sample, the quantity and quality (humification index, HIX) of water extractable organic matter (WEOM) were measured concomitantly with soil enzyme activities (alkaline phosphatase, β-glucosidase, protease) and microbial community size (C_mic). Furthermore, microbial community structure was characterised based on the fingerprints of nucleic acids (DNA) as well as phospholipid fatty acids (PLFA). We observed strong influences of sampling date and depth on the measured parameters, with depth accounting for more of the observed variability than date. Increasing depth resulted in decreases in all parameters, while seasonal effects differed among variants. Principal component (PC) analysis revealed that both DNA and PLFA fingerprints differentiated among microbial communities from different depths, and to a smaller extent, sampling dates. The majority of the 10 PLFAs contributing most to PC 1 were specific for anaerobes. Enzyme activities were strongly related to C_mic, which was depending on water extractable organic carbon and nitrogen (WEOC and WEON) but not to HIX. HIX and WEOM interact with the microbial community, illustrated by (1) the correlation with the number of PLFA peaks (community richness), and (2) the correlations with community PC analysis scores.     

Rhizosphere priming of soil organic matter by bacterial groups in a grassland soil

Plants often impact the rate of native soil organic matter turnover through root interactions with soil organisms; however the role of root-microbial interactions in mediation of the “priming effect” is not well understood. We examined the effects of living plant roots and N fertilization on belowground C dynamics in a California annual grassland soil (Haploxeralf) during a two-year greenhouse study. The fate of ¹³C-labeled belowground C (roots and organic matter) was followed under planted (Avena barbata) and unplanted conditions, and with and without supplemental N (20 kg N ha⁻¹ season⁻¹) over two periods of plant growth, each followed by a dry, fallow period of 120 d. Turnover of belowground ¹³C SOM was followed using ¹³C-phospholipid fatty acid (PLFA) biomarkers. Living roots increased the turnover and loss of belowground ¹³C compared with unplanted soils. Planted soils had 20% less belowground ¹³C present than in unplanted soils after 2 cycles of planting and fallow. After 2 treatment cycles, unlabeled soil C was 4.8% higher in planted soils than unplanted. The addition of N to soils decreased the turnover of enriched belowground ¹³C during the first treatment season in both planted and unplanted soils, however no effect of N was observed thereafter. Our findings suggest that A. barbata may increase soil C levels over time because root and exudate C inputs are significant, but that increase will be moderated by an overall faster C mineralization rate of belowground C. N addition may slow soil C losses; however, the effect was minor and transient in this system. The labeled root-derived ¹³C was initially recovered in gram negative (highest enrichment), gram positive, and fungal biomarkers. With successive growing seasons, the labeled C in the gram negative and fungal markers declined, while gram positive markers continued to accumulate labeled belowground C. The rhizosphere of A. barbata shifted the microbial community composition, resulting in greater abundances of gram negative markers and lower abundances of gram positive, actinobacteria and cyclopropyl PLFA markers compared to unplanted soil. However, the longer-term utilization of labeled belowground C by gram positive bacteria was enhanced in the rhizosphere microbial community compared with unplanted soils. We suggest that the activities of gram positive bacteria may be major controllers of multi-year rhizosphere-related priming of SOM decomposition.     

A call to investigate drivers of soil organic matter retention vs. mineralization in a high CO2 world

Understanding how elevated atmospheric CO₂ alters the formation and decomposition of soil organic carbon (SOC) is important but challenging. If elevated CO₂ induces even small changes in rates of formation or decay of SOC, there could be substantial feedbacks on the atmosphere's concentration of CO₂. However, the long turnover times of many SOC pools - decades to centuries - make the detection of changes in the soil's pool size difficult. Long-term CO₂ enrichment experiments have offered unprecedented opportunities to explore these issues in intact ecosystems for more than a decade. Increased NPP with elevated CO₂ has prompted the hypothesis that SOC may increase at the same time that increased vegetation nitrogen (N) uptake and accumulation indicates probable declines in SON. Varying investigators thus have hypothesized that SOC will increase and SON will decline to explain increased NPP with elevated CO₂; researchers also invoke biogeochemical theory and stoichiometric constraints to argue for strong limitations on the co-occurrence of these phenomena. We call for researchers to investigate two broad research questions to elucidate the drivers of these processes. First, we ask how elevated CO₂ influences compound structure and stoichiometry of that proportion of NPP retained by soil profiles for relatively long time periods. We also call for investigations of the mechanisms underlying the decomposition of mineralizable organic matter with elevated CO₂. Specifically, we need to understand how elevated CO₂ influences microbial priming (driven by enhanced microbial energy needs associated with increases in biomass or activity) and microbial mining of N (driven by enhanced microbial N demand associated with greater vegetative N uptake), two processes that necessarily will be constrained by the stoichiometry of both substrates and microbial demands. Applying technologies such as nuclear magnetic resonance and the detection of biomarkers that reveal organic matter structure and origins, and studying microbial stoichiometric constraints, will dramatically improve our ability to predict future patterns of ecosystem C and N cycling.     

Biochemical analysis of soil organic matter and microbial biomass composition—a pilot study

Biochemical composition of both intracellular (biomass) and extracellular soil organic matter was determined after extraction with 0.5 M K₂SO₄. Extractable carbon, hexoses, pentoses, total reducing sugars, ninhydrin-reactive nitrogen (NRN), proteins and DNA content were colorimetrically determined. The objective of the pilot study was to examine the information potential included in newly measured biochemical characteristics, their environmental variance and the relationships with main soil properties. Correlation analysis and PCA showed independence between biochemical parameters and physico-chemical properties of the soil. Thus, the parameters characterising biochemical composition of the soil biomass and extracellular matter seem to bring new information about the soils beyond the physico-chemical parameters. They also seem to reveal a more detailed view on microbial biomass or extracellular organic matter pool than C_bio or C_ext alone, respectively. The variance, which occurred in biochemical characteristics, also displayed a high discrimination potential between the defined soil categories. Three types of indices were newly proposed: index I (“substrate quantity index”)—the biomass-specific amount of the extracellular organic compounds, index II (“immobilisation ratio”)—the portion of the organic compound immobilised in microbial biomass, and index III (“substrate quality index”)—the extracellular organic compound content related to extracellular organic carbon. The indices displayed a higher potential than both soil biotic and abiotic parameters to discriminate soil characters and soil types.     

The contribution of biogas residues to soil organic matter formation and CO2 emissions in an arable soil

The biogas production process generates as side-products biogas residues containing microbial biomass which could contribute to soil organic matter formation or induce CO₂ emissions when applied to arable soil as fertilizer. Using an isotope labelling approach, we labelled the microbial biomass in biogas residues, mainly G⁺ bacteria and methanogenic archaea via KH¹³CO₃, and traced the fate of microbial biomass carbon in soil with an incubation experiment lasting 378 days. Within the first seven days, 40% of the carbon was rapidly mineralized and after that point mineralization continued, reaching 65% by the end of the experiment. Carbon mineralization data with 93% recovery could be fitted to a two-pool degradation model which estimated proportions and degradation rate constants of readily and slowly degrading pools. About 49% of the carbon was in the slowly degrading pool with a half-life of 1.9 years, suggesting mid-term contribution to living and non-living soil organic matter formation. Biogas residues caused a priming effect at the beginning, thus their intensive application should be avoided.     

Use of organic carbon and loss-on-ignition to estimate soil organic matter in different soil types and horizons

Summary Loss-on-ignition (LOI) and the organic C content have been used to estimate soil organic matter. Organic matter is often estimated from organic C by applying a factor of 1.724. Several authors have examined the relationship between LOI, used as an estimate of organic matter, and C by simple linear regressions. In the present study, this approach was examined in relation to two sets of data. LOI overestimates organic matter in soils with significant proportions of clay minerals because of bound water, and correcting for bound water gives some LOI: C ratios of less than 1. It is concluded that differences in the nature of the organic matter in different soils and horizons make the simple regression approach unsuitable. More attention needs to be paid to studies of the nature of the organic matter.     

The proportional mineralisation of microbial biomass and organic matter caused by air-drying and rewetting of a grassland soil

During the first few days after rewetting of an air-dried soil (AD-RW), microbial activity increases compared to that in the original moist soil, causing increased mineralisation (a flush) of soil organic carbon (C) and other nutrients. The AD-RW flush is believed to be derived from the enhanced mineralisation of both non-biomass soil organic matter (due to its physical release and enhanced availability) and microbial biomass killed during drying and rewetting. Our aim was to determine the effects of AD-RW on the mineralisation of soil organic matter and microbial biomass during and after repeated AD-RW cycles and to quantify their proportions in the CO₂-C flushes that resulted. To do this, a UK grassland soil was amended with ¹⁴C-labelled glucose to label the biomass and then given five AD-RW cycles, each followed by 7 d incubation at 25 °C and 50% water holding capacity. Each AD-RW cycle increased the amount of CO₂-C evolved (varying from 83 to 240 μg g⁻¹ soil), compared to the control with, overall, less CO₂-C being evolved as the number of AD-RW cycles increased. In the first cycle, the amount of biomass C decreased by 44% and microbial ATP by 70% while concentrations of extractable C nearly doubled. However, all rapidly recovered and within 1.3 d after rewetting, biomass C was 87% and ATP was 78% of the initial concentrations measured prior to air-drying. Similarly, by 2 d, extractable organic C had decreased to a similar concentration to the original. After the five AD-RW cycles, the amounts of total and ¹⁴C-labelled biomass C remaining in the soil accounted for 60 and 40% of those in the similarly incubated control soil, respectively. Soil biomass ATP concentrations following the first AD-RW cycle remained remarkably constant (ranging from about 10 to 14 μmol ATP g⁻¹ biomass C) and very similar to the concentration in the fresh soil prior to air-drying. We developed a simple mathematical procedure to estimate the proportion of CO₂-C derived from biomass C and non-biomass C during AD-RW. From it, we estimate that, over the five AD-RW cycles, about 60% of the CO₂-C evolved came from mineralisation of non-biomass organic C and the remainder from the biomass C itself.     

The priming potential of biochar products in relation to labile carbon contents and soil organic matter status

Recognition of biochar as a potential tool for long-term carbon sequestration with additional agronomic benefits is growing. However, the functionality of biochar in soil and the response of soils to biochar inputs are poorly understood. It has been suggested, for example, that biochar additions to soils could prime for the loss of native organic carbon, undermining its sequestration potential. This work examines the priming potential of biochar in the context of its own labile fraction and procedures for their assessment. A systematic set of biochar samples produced from C4 plant biomass under a range of pyrolysis process conditions were incubated in a C3 soil at three discrete levels of organic matter status (a result of contrasting long-term land management on a single site). The biochar samples were characterised for labile carbon content ex-situ and then added to each soil. Priming potential was determined by a comparison of CO₂ flux rates and its isotopic analysis for attribution of source. The results conclusively showed that while carbon mineralisation was often higher in biochar amended soil, this was due to rapid utilisation of a small labile component of biochar and that biochar did not prime for the loss of native organic soil organic matter. Furthermore, in some cases negative priming occurred, with lower carbon mineralisation in biochar amended soil, probably as a result of the stabilisation of labile soil carbon.     

Testing a practical indicator for changing soil organic matter

Long-term changes in soil organic carbon (SOC) resulting from management change are documented for many experimental situations, and corresponding trends in the field have been observed by national survey. Since these changes are relevant to atmospheric carbon balance a practical measure to confirm the impact of recent management decisions at any location, without resorting to repeated sampling, is highly attractive but none has previously been tested. This study assessed intra-aggregate C to fulfil the role, based on a temporary deviation from its predictable contribution to total SOC under stable management. A total of 166 surface soil samples (0–15 cm) were analyzed for intra-aggregate C using an established physical fractionation protocol or compatible scaled-up procedure. Soils were arable (or ley-arable) managed by conventional or minimum-tillage, or permanent grassland, and assigned ‘stable’ or ‘changing’ status on the basis of a verbal account of management history. Log-normal populations of intra-aggregate C were compared for soils of stable and changing status using F-tests. Intra-aggregate C shows promise as an indicator of changing SOC in arable soils up to 30% clay content, particularly soils <20% clay. A larger dataset is required to establish its utility in grassland soils. It is not certain that intra-aggregate C is capable of confirming direction of change or trajectory (endpoint), and functions to indicate change, rather than confirm stable status. Supplementary information on the history of soil use and management is therefore essential in the interpretation of such measurements.     

Responses of soil organic matter and greenhouse gas fluxes to soil management and land use changes in a humid temperate region of southern Europe

We studied the effects of soil management and changes of land use on soils of three adjacent plots of cropland, pasture and oak (Quercus robur) forest. The pasture and the forest were established in part of the cropland, respectively, 20 and 40 yr before the study began. Soil organic matter (SOM) dynamics, water-filled pore space (WFPS), soil temperature, inorganic N and microbial C, as well as fluxes of CO₂, CH₄ and N₂O were measured in the plots over 25 months. The transformation of the cropland to mowed pasture slightly increased the soil organic and microbial C contents, whereas afforestation significantly increased these variables. The cropland and pasture soils showed low CH₄ uptake rates (<1 kg C ha⁻¹ yr⁻¹) and, coinciding with WFPS values >70%, episodes of CH₄ emission, which could be favoured by soil compaction. In the forest site, possibly because of the changes in soil structure and microbial activity, the soil always acted as a sink for CH₄ (4.7 kg C ha⁻¹ yr⁻¹). The N₂O releases at the cropland and pasture sites (2.7 and 4.8 kg N₂O-N ha⁻¹ yr⁻¹) were, respectively, 3 and 6 times higher than at the forest site (0.8 kg N₂O-N ha⁻¹ yr⁻¹). The highest N₂O emissions in the cultivated soils were related to fertilisation and slurry application, and always occurred when the WFPS >60%. These results show that the changes in soil properties as a consequence of the transformation of cropfield to intensive grassland do not imply substantial changes in SOM or in the dynamics of CH₄ and N₂O. On the contrary, afforestation resulted in increases in SOM content and CH₄ uptake, as well as decreases in N₂O emissions.     

Carbon and nitrogen in operationally defined soil organic matter pools

Humic substances [humic acid (HA), fulvic acid (FA), and insoluble humin], particulate organic matter (POM), and glomalin comprise the majority (ca 75%) of operationally defined extractable soil organic matter (SOM). The purpose of this work was to compare amounts of carbon (C) and nitrogen (N) in HA, FA, POM, and glomalin pools in six undisturbed soils. POM, glomalin, HA, and FA in POM, and glomalin, HA, and FA in POM-free soil were extracted in the following sequence: (1) POM fraction separation from the soil, (2) glomalin extraction from the POM fraction and POM-free soil, and (3) co-extraction of HA and FA from the POM fraction and POM-free soil. Only trace amounts of HA and FA were present in the POM fraction, while POM-associated glomalin (POM-glomalin) and POM alone contributed 2 and 12%, respectively, of the total C in the soil. Mean combined weights for chemically extracted pools from POM and from POM-free soil were 9.92 g glomalin, 1.12 g HA, and 0.88 g FA kg⁻¹ soil. Total protein and C, N, and H concentrations showed that glomalin and HA were, for the most part, separate pools, although protein was detected in HA extracts. Even though percentage carbon was higher in HA than in glomalin, glomalin was a larger (almost nine times) operationally defined pool of soil organic C. Glomalin was also the largest pool of soil N of all the pools isolated, but all pools combined only contained 31% of the total N in the soil.     

Influence of inorganic fertilizers and organic amendments on soil organic matter and soil microbial properties under tropical conditions

 Soil organic matter level, mineralizable C and N, microbial biomass C and dehydrogenase, urease and alkaline phosphatase activities were studied in soils from a field experiment under a pearl millet-wheat cropping sequence receiving inorganic fertilizers and a combination of inorganic fertilizers and organic amendments for the last 11 years. The amounts of soil organic matter and mineralizable C and N increased with the application of inorganic fertilizers. However, there were greater increases of these parameters when farmyard manure, wheat straw or Sesbania bispinosa green manure was applied along with inorganic fertilizers. Microbial biomass C increased from 147 mg kg^–1 soil in unfertilized soil to 423 mg kg^–1 soil in soil amended with wheat straw and inorganic fertilizers. The urease and alkaline phosphatase activities of soils increased significantly with a combination of inorganic fertilizers and organic amendments. The results indicate that soil organic matter level and soil microbial activities, vital for the nutrient turnover and long-term productivity of the soil, are enhanced by use of organic amendments along with inorganic fertilizers. Received: 6 May 1998     

县域尺度土壤有机碳储量估算的样点密度优化

县域是我国国家尺度土壤碳库估算的基本地域单元,合理的土壤样品采集密度是保证估算精度要求的基础。以桃源县为例,设置4.70、0.90、0.60、0.40、0.25、0.15、0.10和0.05个km-2共8个样点密度梯度,利用经典统计学和地统计学方法,研究样点密度对县域尺度土壤有机碳库估算精度的影响。经典统计表明,随着样点密度的降低,重复抽样下土壤有机碳均值及其变异系数的波动逐渐增大,标准误差呈幂函数增加(Y=0.025X-0.47,R2=0.97,p0.01)。地统计学分析表明,随着样点密度的降低,块金值和基底效应逐渐增加,偏基台、变程和决定系数的波动幅度逐渐增大,拟合残差呈幂函数增加(Y=0.001 4X-1.66,R2=0.56,p0.05);土壤有机碳空间分布的局部差异逐渐被弱化,重复抽样下县域土壤有机碳库储量及其平均误差的波动逐渐增强,均方根误差呈幂函数增加(Y=0.77X-0.05,R2=0.59,p0.05)。从整体上看,样点密度小于0.15个km-2时,以上变化均急剧增强,土壤碳储量估算的精度快速降低。因此,综合科学、高效和经济方面的考虑,估算县域农田表层土壤有机碳储量的最佳样点密度为0.15个km-2。本研究结果可为开展区域尺度土壤有机碳野外调查提供辅助支持。     

The influence of organic matter in reducing the destabilization of soil by simulated tillage

Different agricultural practices can result in a decline in soil organic carbon (SOC) and a consequent reduction in soil structural stability. Experiments were conducted on soils with a range of SOC values, to quantify the destabilizing effects of increased tillage intensity. Different tillage intensity was simulated with the use of a falling weight, where specific energy levels, similar to those experienced during tillage, were reproduced. The level of destabilization was assessed by the quantity of mechanically dispersed clay (using a turbidimetric technique) and the quantity of water-stable aggregates (WSA) > 0.25 mm remaining after being shaken in water.

The quantity of clay dispersed increased with increasing water content, in the absence of any mechanical pretreatment, the rate of increase rising sharply with declining SOC. Following simulated tillage, and at water contents above the plastic limit, clay dispersion increased in proportion to the energy of disruption, and also increased with decreasing SOC levels. Below the plastic limit all the soils were relatively insensitive to mechanical disruption. A simple empirical model was derived to link clay dispersion to SOC, water content and energy of disruption.

The proportion of WSA declined sharply with decreasing SOC, and to a lesser extent following tillage. The quantity of WSA following simulated intensive tillage (300 J kg⁻¹) of grassland (SOC, 2.8–3.2 g (100 g)⁻¹) was greater than that present, prior to tillage from fallow, arable and arable/ley rotation treatments (SOC 1.1–2.5 g (100 g)⁻¹). Aggregate tensile strength was found to be relatively insensitive to differences in SOC. However, variations of strength within treatments, an indicator of soil friability, increased in proportion with SOC. A turbidity index was derived in which the turbidity of natural and remoulded aggregates was compared. Variation of this index with increasing mechanical energy is used as an indicator of the sensitivity of soils to damage during tillage. A visual representation is constructed to link the sensitivity of soils to damage during tillage with both SOC and water potential. These experiments illustrate that management practices, which lead to a long term reduction in SOC, are responsible for an increase in aggregate strength and reduction in stability plus an increase in sensitivity of soils to structural decline following subsequent tillage.     

Water infiltration and soil structure related to organic matter and its stratification with depth

Soil organic matter is a key attribute of soil quality that impacts soil aggregation and water infiltration. Two soils (Typic Kanhapludults), one under long-term management of conventional tillage (CT) and one under long-term management of no tillage (NT), were sampled to a depth of 12 cm. Soil cores (15 cm diameter) were either left intact or sieved and repacked to differentiate between short-term (sieving) and long-term (tillage management) effects of soil disturbance on water infiltration, penetration resistance, soil bulk density, macroaggregate stability, and soil organic carbon (SOC). Mean weekly water infiltration was not different between sieved and intact cores from long-term CT (22 cm h⁻¹), but was significantly greater in intact (72 cm h⁻¹) than in sieved (28 cm h⁻¹) soil from long-term NT. The stratification ratio of SOC (i.e., of 0–3 cm depth divided by that of 6–12 cm depth) was predictive of water infiltration rate, irrespective of short- or long-term history of disturbance. Although tillage is used to increase soil porosity, it is a short-term solution that has negative consequences on surface soil structural stability, surface residue accumulation, and surface-SOC, which are critical features that control water infiltration and subsequent water transmission and storage in soil. The stratification ratio of SOC could be used as a simple diagnostic tool to identify land management strategies that improve soil water properties (e.g., infiltration, water-holding capacity, and plant-available water).     

Biochemical properties and biodegradation of dissolved organic matter from soils

Various biologically mediated processes are involved in the turnover of dissolved organic matter (DOM) in soil; however, relatively little is known about the dynamics of either the microbial community or the individual classes of organic molecules during the decomposition of DOM. We examined the net loss of DOC, the mineralisation of C to CO₂ and the degradation of DOC from six different soils by soil microorganisms. We also quantified the changes in the concentrations of protein, carbohydrate and amino acid C during microbial biodegradation. Over a 70-day incubation period at 20°C, the mineralisation of DOC to CO₂ was described by a double exponential model with a labile pool (half-life, 3–8 days) and a stable pool (half-life, 0.4–6 years). However, in nearly all cases, the mass loss of DOC exceeded the C released as CO₂ with significant deviations from the double exponential model. Comparison of mass DOC loss, CO₂ production and microbial cell counts, determined by epifluorescence microscopy, showed that a proportion of the lost DOC mass could be accounted for by microbial assimilation. Carbohydrate and protein C concentrations fluctuated throughout the incubation with a net change of between 3 to 13 and −30 to 22.4% initial DOC, respectively. No amino acid C was detected during the incubation period (level of detection, 0.01 mg C l⁻¹).