Effects of addition of maize litter and earthworms on C mineralization and aggregate formation in single and mixed soils differing in soil organic carbon and clay content

C mineralization and aggregate stability directly depend upon organic matter and clay content, and both processes are influenced by the activity of microorganisms and soil fauna. However, quantitative data are scarce. To achieve a gradient in C and clay content, a topsoil was mixed with a subsoil. Single soils and the soil mixture were amended with 1.0 mg maize litter C g soil⁻¹ with and without endogeic earthworms (Aporrectodea caliginosa). The differently treated soils were incubated for 49 days at 15 °C and 40% water holding capacity. Cumulative C mineralization, microbial biomass, ergosterol content and aggregate fractions were investigated and litter derived C in bulk soil and aggregates were determined using isotope analyses. Results from the soil mixture were compared with the calculated mean values of the two single soils. Mixing of soil horizons differing in carbon and clay content stimulated C mineralization of added maize residues as well as of soil organic matter. Mixing also increased contents of macro-aggregate C and decreased contents of micro-aggregate C. Although A. caliginosa had a stimulating effect on C mineralization in all soils, decomposition of added litter by A. caliginosa was higher in the subsoil, whereas A. caliginosa decreased litter decomposition in the soil mixture and the topsoil. Litter derived C in macro-aggregates was higher with A. caliginosa than with litter only. In the C poor subsoil amended with litter, A. caliginosa stimulated the microbial community as indicated by the increase in microbial biomass. Furthermore, the decrease of ergosterol in the earthworm treated soils showed the influence of A. caliginosa on the microbial community, by reducing saprotrophic fungi. Overall, our data suggest both a decrease of saprotrophic fungi by selective grazing, burrowing and casting activity as well as a stimulation of the microbial community by A. caliginosa.     

Near infrared reflectance spectroscopy: A tool to characterize the composition of different types of exogenous organic matter and their behaviour in soil

In addition to total organic carbon and nitrogen, potential organic carbon mineralization under controlled laboratory conditions and indicators such as the indicator of remaining organic carbon in soil (I_ROC), based on Van Soest biochemical fractionation and short-term carbon mineralization in soil, are used to predict the evolution of exogenous organic matter (EOM) after its application to soils. The purpose of this study was to develop near infrared reflectance spectroscopy (NIRS) calibration models that could predict these characteristics in a large dataset including 300 EOMs representative of the broad range of such materials applied to cultivated soils (plant materials, animal manures, composts, sludges, etc.). The NIRS predictions of total organic matter and total organic carbon were satisfactory (R²_P = 0.80 and 0.85, ratio of performance to deviation, RPD_P = 2.2 and 2.6, respectively), and prediction of the Van Soest soluble, cellulose and holocellulose fractions were acceptable (R²_P = 0.82, 0.73 and 0.70, RPD_P = 2.3, 1.9 and 1.8, respectively) with coefficients of variation close to those of the reference methods. The NIRS prediction of carbon mineralization during incubation was satisfactory and indeed better regarding the short-term results of mineralization (R²_P = 0.78 and 0.78, and RPD_P = 2.1 and 2.0 for 3 and 7 days of incubation, respectively). The I_ROC indicator was predicted with fairly good accuracy (R²_P = 0.79, RPD_P = 2.2). Variables related to the long-term C mineralization of EOM in soil were not predicted accurately, except for I_ROC which was based on analytical and well-identified characteristics, probably because of the increasing interactions and complexity of the factors governing EOM mineralization in soil as a function of incubation time. This study demonstrated the possibility of developing NIRS predictive models for EOM characteristics in heterogeneous datasets of EOMs. However, specific NIRS predictive models still remain necessary for sludges, organo-mineral fertilizers and liquid manures.     

Soil aggregation and organic carbon in short-term stockpiles

Surface mining is known to drastically reduce soil organic carbon (OC) pools through various mechanisms associated with topsoil salvage, stockpiling and respreading. Stockpiling is an important management practice; however, the effects of this practice on reductions and recovery of soil aggregation and aggregate OC are poorly understood. Objectives of this research were to monitor soil aggregation and aggregate OC in the surface of a short‐term stockpile (<3 yr) followed by a second movement of stockpiled soils to a temporary location. Samples were analysed for aggregate size distribution, aggregate fractions, OC, and organic matter turnover using ¹³C natural abundance. Macroaggregate proportions increased and microaggregate proportions decreased after 3 yr of storage, possibly indicating recovery of soil structure. Following the removal of the stockpile and placement in a temporary pile, macroaggregation decreased and free silt and clay fractions increased relative to initially stockpiled soils. The second disturbance resulted in greater destruction of aggregate structure than the initial disturbance during topsoil salvage. Aggregate organic matter (as indicated by OC) increased significantly between the early sampling of the stockpiled soils (<1 yr in storage) and the placement of the topsoil in a temporary pile in macroaggregates and remained the same for microaggregates. Organic matter not protected within aggregates decreased with storage time as this material was available for utilization by microbes while aggregate protected organic matter (OM) remained unchanged or slightly increased for macro‐ and microaggregates with stockpile storage time. Aggregate δ¹³C values did not indicate inclusion of new OM within soil aggregates after 3 yr of topsoil stockpiling. Short‐term stockpiling was beneficial for aggregation in the surface layers where plant roots and microbial communities were active; however, subsequent movement of the topsoil resulted in a greater loss of soil aggregation relative to the initial topsoil salvage without impacting soil OC.     

The effect of maize straw placement on mineralization of C and N in soil particle size fractions

Fundamental knowledge about the complex processes during the decomposition, mineralization and transfer of residue organic matter in soils is essential to assess risks of changes in agricultural practices. In a double tracer (¹³C, ¹⁵N) experiment the effect of maize straw on the mineralization dynamics and on the distribution of maize-derived organic matter within particle size fractions was investigated. Maize straw (a C₄ plant) labelled with ¹⁵N was added to soils (13.2 g dry matter kg^–1 soil) which previously had grown only C₃ plants, establishing two treatments: (i) soil mixed with maize straw (mixed), and (ii) soil with maize straw applied on the surface (surface). Samples were incubated in the laboratory at 14°C for 365 days. The size fractions (> 200 μm, 200–63 μm, 63–2 μm, 2–0.1 μm and < 0.1 μm), obtained after low-energy sonication (0.2 kJ g^–1), were separated by a combination of wet-sieving and centrifuging. The mineralization of maize C was similar in the two treatments after one year. However, decomposition of maize particulate organic matter (predominantly in the fraction > 200 μm) was significantly greater in the mixed treatment, and more C derived from the maize was associated with silt- and clay-sized particles. A two-component model fitted to the data yielded a rapidly mineralizable C pool (about 20% of total C) and a slowly mineralizable pool (about 80%). Generally, the size of the rapidly mineralizable C pool was rather small because inorganic N was rapidly immobilized after the addition of maize. However, the different mean half-lives of the C pools (rapidly decomposable mixed 0.035 years, and surface-applied 0.085 years; slowly decomposable mixed 0.96 years, and surface-applied 1.7 years) showed that mineralization was delayed when the straw was left on the surface. This seems to be because there is little contact between the soil microflora and plant residues. Evidently, the organic matter is more decomposed and protected within soil inorganic compounds when mixed into the soil than when applied on the soil surface, despite similar rates of mineralization.     

Transformation of organic matter from maize residues into labile and humic fractions of three European soils as revealed by 13C distribution and CPMAS-NMR spectra

The dynamics of incorporation of fresh organic residues into the various fractions of soil organic matter have yet to be clarified in terms of chemical structures and mechanisms involved. We studied by ¹³C‐dilution analysis and CPMAS‐¹³C‐NMR spectroscopy the distribution of organic carbon from mixed or mulched maize residues into specific defined fractions such as carbohydrates and humic fractions isolated by selective extractants in a year‐long incubation of three European soils. The contents of carbohydrates in soil particle size fractions and relative δ¹³C values showed no retention of carbohydrates from maize but rather decomposition of those from native organic matter in the soil. By contrast, CPMAS‐¹³C‐NMR spectra of humic (HA) and fulvic acids (FA) extracted by alkaline solution generally indicated the transfer of maize C (mostly carbohydrates and peptides) into humic materials, whereas spectra of organic matter extracted with an acetone solution (HE) indicated solubilization of an aliphatic‐rich, hydrophobic fraction that seemed not to contain any C from maize. The abundance of ¹³C showed that all humic fractions behaved as a sink for C from maize residues but the FA fraction was related to the turnover of fresh organic matter more than the HA. Removal of hydrophobic components from incubated soils by acetone solution allowed a subsequent extraction of HA and, especially, FA still containing much C from maize. The combination of isotopic measurements and NMR spectra indicated that while hydrophilic compounds from maize were retained in HA and FA, hydrophobic components in the HE fraction had chemical features similar to those of humin. Our results show that the organic compounds released in soils by mineralization of fresh plant residues are stored mainly in the hydrophilic fraction of humic substances which are, in turn, stabilized against microbial degradation by the most hydrophobic humic matter. Our findings suggest that native soil humic substances contribute to the accumulation of new organic matter in soils.     

Soil texture and nitrogen mineralization potential across a riparian toposequence in a semi-arid savanna

Soil texture is an important influence on nutrient cycling in upland soils, with documented relationships between mineral particle size distribution and organic matter retention, nitrogen (N) mineralization, microbial biomass and other soil properties. However, little is known of the role of mineral particle size in riparian soils, where fluvial sorting creates strong spatial contrasts in the size distribution of sediments in sedimentary landforms. We studied total organic carbon (TOC) and total N (TN) storage and net N mineralization relative to soil texture and landform in soils of a riparian toposequence along the Phugwane River in Kruger National Park, South Africa. TOC, TN and potential N mineralization related strongly to particle size distribution in all soils along the toposequence. TOC and TN were positively correlated with silt and clay concentration (r² =0.78). In long-term laboratory incubations, N mineralization was greatest in fine-textured, N-rich soils, although the proportions of soil N mineralized were inversely related to fine particle concentrations (r²=0.61). There were differences in TOC, TN and potential N mineralization among landform types, but none of these soil properties were statistically significant after accounting for the effect of particle size. These results demonstrate the influence of particle size in mediating N retention and mineralization in these soils. Predictable differences in soil texture across alluvial landforms contribute to corresponding contrasts in soil conditions, and may play an important role in structuring riparian soil and plant communities.     

Organic matter turnover in soil physical fractions following woody plant invasion of grassland: Evidence from natural C and N

Soil physical structure causes differential accessibility of soil organic carbon (SOC) to decomposer organisms and is an important determinant of SOC storage and turnover. Techniques for physical fractionation of soil organic matter in conjunction with isotopic analyses (δ¹³C, δ¹⁵N) of those soil fractions have been used previously to (a) determine where organic C is stored relative to aggregate structure, (b) identify sources of SOC, (c) quantify turnover rates of SOC in specific soil fractions, and (d) evaluate organic matter quality. We used these two complementary approaches to characterize soil C storage and dynamics in the Rio Grande Plains of southern Texas where C₃ trees/shrubs (δ¹³C=−27‰) have largely replaced C₄ grasslands (δ¹³C=−14‰) over the past 100-200 years. Using a chronosequence approach, soils were collected from remnant grasslands (Time 0) and from woody plant stands ranging in age from 10 to 130 years. We separated soil organic matter into specific size/density fractions and determined their C and N concentrations and natural δ¹³C and δ¹⁵N values. Mean residence times (MRTs) of soil fractions were calculated based on changes in their δ¹³C with time after woody encroachment. The shortest MRTs (average=30 years) were associated with all particulate organic matter (POM) fractions not protected within aggregates. Fine POM (53-250 μm) within macro- and microaggregates was relatively more protected from decay, with an average MRT of 60 years. All silt+clay fractions had the longest MRTs (average=360 years) regardless of whether they were found inside or outside of aggregate structure. δ¹⁵N values of soil physical fractions were positively correlated with MRTs of the same fractions, suggesting that higher δ¹⁵N values reflect an increased degree of humification. Increased soil C and N pools in wooded areas were due to both the retention of older C₄-derived organic matter by protection within microaggregates and association with silt+clay, and the accumulation of new C₃-derived organic matter in macroaggregates and POM fractions.     

Cultivation effects on temporal changes of organic carbon and aggregate stability in desert soils of Hexi Corridor region in China

Sustainable agricultural use of cultivated desert soils has become a concern in Hexi Corridor in Gansu Province of China, because loss of topsoil in dust storms has been recently intensified. We chose four desert sites to investigate the effects of cultivation (cropping) on (i) soil organic C and its size fractions and (ii) soil aggregate stability (as a measure of soil erodibility). These parameters are of vital importance for evaluating the sustainability of agricultural practices.Total organic C as well as organic C fractions in soil (coarse organic C, 0.1–2 mm; young organic C, 0.05–0.1 mm; stable organic C, <0.05 mm) generally increased with the duration of the cultivation period from 0 (virgin soil, non-cultivated) to more than 30 years (p < 0.05). Compared to total organic C in virgin soils (2.3–3.5 g kg⁻¹ soil), significantly greater values were found after 10 to >20 years of cultivation (6.2–7.1 g kg⁻¹ soil). The increase in organic C in desert soils following prolonged cultivation was mainly the consequence of an increase in the coarse organic C. The increase in total organic C in soil was also dependent on clay content [total organic C = 0.96 + 0.249 clay content (%) + 0.05 cultivation year, R² = 0.48, n = 27, p < 0.001]. This indicates that clay protected soil organic C from mineralization, and also contributed to the increase in soil organic C as time of cultivation increased.There was a significant positive correlation between aggregate stability and total organic C across all field sites. The water stability of aggregates was low (with water-stable aggregate percentage ∼4% of dry-sieved aggregates of size 1–5 mm). There was no consistent pattern of increase in the soil aggregate stability with time of cultivation at different locations, suggesting that desert soils might remain prone to wind erosion even after 50 years of cultivation. Alternative management options, such as retaining harvested crop residues on soil surface and excluding or minimizing tillage, may permit sustainable agricultural use of desert soils.     

Predicting soil N mineralization using organic matter fractions and soil properties: A re-analysis of literature data

Extractable organic matter (EOM) fractions have been used to assess the capacity of soils to supply nitrogen (N), but their role in N mineralization and their potential to improve agricultural fertilizer management are still under debate. This paper shows evidence that the relationship between EOM and soil N supply is an indirect relationship reflecting the soils' organic matter content. Data from 59 published experiments were re-analyzed using multivariate PLS modelling. Nitrogen mineralization was primarily related to the size of total and extractable organic matter fractions whereas variables reflecting soil texture and organic matter quality were less important. All EOM fractions reflected the soil organic matter content of the soil rather than a specific bioavailable fraction. There is strong need for research that explores the biochemical basis for relationships among total organic matter, extractable organic matter and soil N mineralization using mechanistic approaches.     

Organic matter characteristics and C and N transformations in the humus layer under two tree species, Betula pendula and Picea abies

The aim of this study was to compare the effects of silver birch (Betula pendula Roth) and Norway spruce (Picea abies (L.) Karst.) on soil C and N transformations and on the characteristics of organic matter. Soil samples were taken from the humus layer of a replicated 35-year-old birch-spruce field experiment growing on Vaccinium myrtillus site type in middle-eastern Finland. The soil was a podzol and humus type mor. Soil pH was higher under birch (4.7) than under spruce (4.1). The C-to-N ratio was lower under birch (17) than under spruce (23). Per unit organic matter, microbial biomass C and N, net N mineralization and net nitrification were all higher in birch soil than in spruce soil. The rate of C mineralization (CO₂ production) was, however, the same regardless of tree species. Water-extracts were analyzed for the concentrations of dissolved organic C (DOC) and N (DON) and characterized according to molecular size distribution by ultrafiltration and according to chemical composition using a resin fractionation technique. The concentration of DON, in particular, was higher in birch soil than in spruce soil. The distribution of DOC and DON into different fractions based on molecular size or chemical composition was rather similar in both soils. The concentration of total phenolics, expressed as tannic acid equivalents, was higher in the humus layer under birch than in the humus layer under spruce, because the birch humus layer contained significantly more low-molecular weight (about <0.5 kD) phenolics than the spruce humus layer did. The concentration of proanthocyanidins (condensed tannins) was higher in spruce soil than in birch soil. The concentrations of the five most abundant phenolic acids showed that ferulic and p-coumaric acids were more abundant in spruce soil. Birch soil tended to contain slightly more nonvolatile sesquiterpenes than the spruce soil. The concentration of diterpenes was similar in both soils; but birch soil contained significantly more triterpenes, mainly sterols, than spruce soil did.     

Carbon, nitrogen and temperature controls on microbial activity in soils from an Antarctic dry valley

The Antarctic dry valleys are characterized by extremely low temperatures, dry conditions and lack of conspicuous terrestrial autotrophs, but the soils contain organic C, emit CO₂ and support communities of heterotrophic soil organisms. We have examined the role of modern lacustrine detritus as a driver of soil respiration in the Garwood Valley, Antarctica, by characterizing the composition and mineralization of both lacustrine detritus and soil organic matter, and relating these properties to soil respiration and the abiotic controls on soil respiration. Laboratory mineralization of organic C in soils from different, geomorphically defined, landscape elements at 10 °C was comparable with decomposition of lacustrine detritus (mean residence times between 115 and 345 d for the detritus and 410 and 1670 d for soil organic matter). The chemical composition of the detritus (C-to-N ratio=9:1-12:1 and low alkyl-C-to-O-alkyl-C ratio in solid-state ¹³C nuclear magnetic resonance spectroscopy) indicated that it was a labile, high quality resource for micro-organisms. Initial (0-6 d at 10 °C) respiratory responses to glucose, glycine and NH₄Cl addition were positive in all the soils tested, indicating both C and N limitations on soil respiration. However, over the longer term (up to 48 d at 10 °C) differential responses occurred. Glucose addition led to net C mineralization in most of the soils. In the lake shore soils, which contained accumulated lacustrine organic matter, glucose led to substantial priming of the decomposition of the indigenous organic matter, indicating a C or energetic limitation to mineralization in that soil. By contrast, over 48 d, glycine addition led to no net C mineralization in all soils except stream edge and lake shore soils, indicating either substantial assimilation of the added C (and N), or no detectable utilization of the glycine. The Q₁₀ values for basal respiration over the −0.5-20 °C temperature range were between 1.4 and 3.3 for the different soils, increasing to between 3.4 and 6.9 for glucose-induced respiration, and showed a temperature dependence with Q₁₀ increasing with declining temperature. Taken together, our results strongly support contemporaneous lacustrine detritus, blown from the lake shore, as an important driver of soil respiration in the Antarctic dry valley soils.     

Soil organic matter in soil physical fractions in adjacent semi-natural and cultivated stands in temperate Atlantic forests

Changes from natural tree species to rapidly growing exotic species as well as intensification of forestry operations with heavy machinery can lead to changes in the quantity and quality of organic matter inputs to soil and to disruption of soil physical structure. These two ecosystem properties are tightly linked to organic matter dynamics. Five adjacent forest stands were selected to study soil organic matter dynamics in soil physical fractions. On one hand, two semi-natural broadleaved forests (Quercus robur, Fagus sylvatica) and an adult radiata pine plantation (40-year-old,) in order to study the effect of species change on these parameters, and on the other, a chronosequence of Pinus radiata plantations (40-year-old; 3-year-old; 16-year-old), to study the effect of mechanization during harvesting and intense site preparation. Samples of intact topsoil (0-5 cm) were collected and aggregate-size distribution, mean weight diameter (MWD), total C and N, particulate organic matter (POM)-C, POM-N and microbial biomass-C were determined in each aggregate size fraction. Microbial respiration and nitrogen mineralization were also assessed in each aggregate size fraction, during a 28 day incubation period.Losses of POM-C and POM-N in the bulk soil due to mechanical site preparation were high relative to total soil C and N, which suggests that POM is a sensitive parameter to the effect of mechanization. The ratio C-POM:SOM was significantly related to MWD (R² = 0.75, P < 0.001) reflecting that POM may play a key role in the topsoil aggregate formation in these stands. Semi-natural stands had a higher proportion of macroaggregates (0.25-2 mm) than the cultivated adult one. Megaaggregates (>2 mm) were the most abundant class in mature stands (82-92%), whereas macro- and microaggregates (<2 mm) were the most abundant ones in the intensely soil prepared P. radiata plantation (49%).Indicators for sustainable forest management related to soil organic matter should not only be assessed in terms of total C stocks but also with respect to sensitive organic matter and its degradability in different size classes.     

Evaluating biodegradability of soil organic matter by its thermal stability and chemical composition

The stability of soil organic matter (SOM) as it relates to resistance to microbial degradation has important implications for nutrient cycling, emission of greenhouse gases, and C sequestration. Hence, there is interest in developing new ways to quantify and characterise the labile and stable forms of SOM. Our objective in this study was to evaluate SOM under widely contrasting management regimes to determine whether the variation in chemical composition and resistance to pyrolysis observed for various constituent C fractions could be related to their resistance to decomposition. Samples from the same soil under permanent pasture, an arable cropping rotation, and chemical fallow were physically fractionated (sand: 2000-50 μm; silt: 50-5 μm, and clay: <5 μm). Biodegradability of the SOM in size fractions and whole soils was assessed in a laboratory mineralization study. Thermal stability was determined by analytical pyrolysis using a Rock-Eval pyrolyser, and chemical composition was characterized by X-ray absorption near-edge structure (XANES) spectroscopy at the C and N K-edges. Relative to the pasture soil, SOM in the arable and fallow soils declined by 30% and 40%, respectively. The mineralization bioassay showed that SOM in whole soil and soil fractions under fallow was less susceptible to biodegradation than that in other management practices. The SOM in the sand fraction was significantly more biodegradable than that in the silt or clay fractions. Analysis by XANES showed a proportional increase in carboxylates and a reduction in amides (protein) and aromatics in the fallow whole soil compared to the pasture and arable soils. Moreover, protein depletion was greatest in the sand fraction of the fallow soil. Sand fractions in fallow and arable soils were, however, relatively enriched in plant-derived phenols, aromatics, and carboxylates compared to the sand fraction of pasture soils. Analytical pyrolysis showed distinct differences in the thermal stability of SOM among the whole soil and their size fractions; it also showed that the loss of SOM generally involved preferential degradation of H-rich compounds. The temperature at which half of the C was pyrolyzed was strongly correlated with mineralizable C, providing good evidence for a link between the biological and thermal stability of SOM.     

Straw incorporation and soil organic matter in macro-aggregates and particle size separates

Two field experiments in which straw has been removed or incorporated for 17 yr (loamy sand) and 10 yr (sandy clay loam) were sampled to examine the effect of straw on the C and N contents in whole soil samples, macro-aggregate fractions and primary particle-size separates. The particle size composition of the aggregate fractions was determined. Aggregates were isolated by dry sieving. Straw incorporation increased the number of 1–20 mm aggregates in the loamy sand but no effect was noted in the sandy clay loam. Straw had no effect on the particle size composition of the various aggregate fractions. After correction for loose sand that accumulated in the aggregate fractions during dry sieving, macro-aggregates appeared to be enriched in clay and silt compared with whole soil samples. Because of the possible detachment of sand particles from the exterior surface of aggregates during sieving operations, it was inferred that the particle size composition of macro-aggregates is similar to that of the bulk soil. The organic matter contents of the aggregate fractions were closely correlated with their clay + silt contents. Differences in the organic matter content of clay isolated from whole soil samples and aggregate fractions were generally small. This was also true for the silt-size separates. In both soils, straw incorporation increased the organic matter content of nearly all clay and silt separates; for silt this was generally twice that observed for clay. The amounts of soil C, derived from straw, left in the loamy sand and sandy clay loam at the time of sampling were 4.4 and 4.5 t ha^?1, corresponding to 12 and 21% of the straw C added. The C/N ratios of the straw-derived soil organic matter were 11 and 12 for the loamy sand and sandy clay loam, respectively.     

Comparison of tree species effects on microbial C and N transformations and dissolved organic matter properties in the organic layer of boreal forests

The aim of this study was to determine whether tree species consistently affects soil microbial activities related to C and N cycling and to compare these activities with the characteristics of soil dissolved organic matter (DOM). Samples were taken from the mor-type organic layer (Of+Oh) underlain by podzols of six 20–72-year-old tree-species experiments on different site types in different parts of Finland. Sampling plots were dominated by silver birch (Betula pendula Roth), Norway spruce (Picea abies (L.) Karst) or Scots pine (Pinus sylvestris L., only on four sites). Amounts of C and N in the microbial biomass and rates of C mineralization (CO₂ production) and net N mineralization were determined, and water extracts were analysed for concentrations of DOC and DON and characterized according to molecular size by ultrafiltration and according to chemical composition using a resin fractionation technique. In all older stands, birch, compared to spruce or pine, increased soil pH, NH₄-concentration and amounts of C and N in microbial biomass and decreased the C-to-N ratio and ratio of dissolved organic N (DON)-to-mineral N. Birch had similar effects also in part of the younger stands. Birch also increased the rates of both C and net N mineralization compared to spruce or pine but only on two sites. In all soils, net nitrification was low. The distribution of DOC into different fractions based on chemical composition and molecular size was rather similar in all soils. The most abundant chemical fraction was hydrophobic acids, and the most abundant molecular size fraction was 10–100 kDa. The C-to-N ratio varied but was lowest in hydrophilic bases and in the smallest molecular size class. Mineralization of C was highly and positively correlated with concentration of DOC (Pearson's correlation coefficient r = 0.9, P < 0.01). The results indicated close interactions between microbial processes and dissolved organic matter.     

Storage and stability of organic matter and fossil carbon in a Luvisol and Phaeozem with continuous maize cropping: A synthesis

Quantitative information about the amount and stability of organic carbon (OC) in different soil organic‐matter (OM) fractions and in specific organic compounds and compound‐classes is needed to improve our understanding of organic‐matter sequestration in soils. In the present paper, we summarize and integrate results performed on two different arable soils with continuous maize cropping (a) Stagnic Luvisol with maize cropping for 24 y, b) Luvic Phaeozem with maize cropping for 39 y) to identify (1) the storage of OC in different soil organic‐matter fractions, (2) the function of these fractions with respect to soil‐OC stabilization, (3) the importance and partitioning of fossil‐C deposits, and (4) the rates of soil‐OC stabilization as assessed by compound‐specific isotope analyses. The fractionation procedures included particle‐size fractionation, density fractionation, aggregate fractionation, acid hydrolysis, different oxidation procedures, isolation of extractable lipids and phospholipid fatty acids, pyrolysis, and the determination of black C. Stability of OC was determined by ¹³C and ¹⁴C analyses. The main inputs of OC were plant litter (both sites) and deposition of fossil C likely from coal combustion and lignite dust (only Phaeozem).     

Decomposition of maize straw in three European soils as revealed by DRIFT spectra of soil particle fractions

Diffuse Reflectance Infrared Fourier Transform (DRIFT) technique was used to investigate decomposition of maize straw residues in particle-size fractions of three European soils in a 1-year incubation experiment that simulated both incorporation and mulching practices. The aliphatic bands in the 2920–2860 cm⁻¹ regions were used to derive decomposition curves and mineralization rates of maize residues. Evaluation of soil organic matter changes by DRIFT in particle-size fractions depended on soil texture and soil aggregate stability. Decomposition could be followed over the full incubation period only in three size-fractions of the silty German soil because of its intermediate aggregate stability. DRIFT spectra were not useful in the least stable sandy Danish soil and in the most stable clayey Italian soil. Decomposition rates derived from DRIFT results were similar to those obtained by isotopic techniques. DRIFT spectroscopy may represent a rapid and accurate method to follow fresh organic matter degradation directly in soil matrix or particle-size fractions in some soils provided that adequate soil dispersion is obtained.     

Soil organic matter fractionation as a tool for predicting nitrogen mineralization in silty arable soils

After decades of searching for a practical method to estimate the N mineralization capacity of soil, there is still no consistent methodology. Indeed it is important to have practical methods to estimate soil nitrogen release for plant uptake and that should be appropriate, less time consuming, and cost effective for farmers. We fractionated soil organic matter (SOM) to assess different fractions of SOM as predictors for net N mineralization measured from repacked (disturbed) and intact (undisturbed) soil cores in 14 weeks of laboratory incubations. A soil set consisting of surface soil from 18 cereal and root‐cropped arable fields was physically fractionated into coarse and fine free particulate OM (coarse fPOM and fine fPOM), intra‐microaggregate particulate OM (iPOM) and silt and clay sized OM. The silt and clay sized OM was further chemically fractionated by oxidation with 6% NaOCl to isolate an oxidation‐resistant OM fraction, followed by extraction of mineral bound OM with 10% HF (HF‐res OM). Stepwise multiple linear regression yielded a significant relationship between the annual N mineralization (kg N/ha) from undisturbed soil and coarse fPOM N (kg N/ha), silt and clay N (kg N/ha) and its C:N ratio (R² = 0.80; P < 0.01). The relative annual N mineralization (% of soil N) from disturbed soils was related to coarse fPOM N, HF‐res OC (% of soil organic carbon) and its C:N ratio (R² = 0.83; P < 0.01). Physical fractions of SOM were thus found to be the most useful predictors for estimating the annual N mineralization rate of undisturbed soils. However, the bioavailability of physical fractions was changed due to the disturbance of soil. For disturbed soils, a presumed stable chemical SOM fraction was found to be a relevant predictor indicating that this fraction still contains bio‐available N. The latter prompted a revision in our reasoning behind selective oxidation and extraction as tools for characterizing soil organic N quality with respect to N availability. Nonetheless, the present study also underscores the potential of a combined physical and chemical fractionation procedure for isolating and quantifying N fractions which preferentially contribute to bulk soil N mineralization. The N content or C:N ratio of such fractions may be used to predict N mineralization in arable soils.     

Organic matter in size‐density fractions after 16–50 years of grass ley,cereal cropping and organic amendments

Size‐density fractionation, which was originally developed to examine short‐term decomposition of added material in sandy soil, was highly sensitive to medium‐ to long‐term changes in loam and clay soils. Materials from different size classes (>1 mm, 0.1–1 mm, 0.05–0.1 mm and <0.05 mm) were separated by density into light (ρ < 1.0 g cm⁻³), medium (1.0 < ρ < 1.85 g cm⁻³) and heavy (ρ > 1.85 g cm⁻³) fractions. In 16–18‐year cropping experiments the 0.1–1‐mm heavy fraction contained 17–19% of total carbon in ley soils compared with 7% in continuously cropped soils. Greater N‐mineralization rates after sieving of ley cropped soils could not be related to differences in C:N ratios of fractions, but this was assumed to be related to exposure of aggregate‐binding agents. In a 50‐year trial 40% of total soil carbon was contained in the 0.1–1‐mm heavy fraction in soil treated with sewage sludge compared with 7–9% in the fallow and ‘zero N’ treatments. Thus, the soils studied expressed an aggregate hierarchy dependent on organic carbon dynamics. The relative abundance of carbon in heavy organo‐mineral fractions >0.1 mm was inversely related to the relative abundance of C in black‐brown medium density material <0.1 mm, defined as uncomplexed particulate organic matter that was presumably released during ultrasonic disruption deterioration of finer (<0.1 mm) aggregated organo‐mineral particles. The size density fractionation allowed identification of materials of contrasting visual appearance, chemical qualities and, by inference, biological turnover times. However, they were found to be predominantly composite fractions and may be too complex to be represented by unique model pools.     

Soil organic carbon distribution drives microbial activity and functional diversity in particle and aggregate-size fractions

Chemical and functional characterizations of particle-size and aggregate fractions of soils were performed to investigate whether accessibility and decomposability of organic matter regulate functions and diversity of the soil microbial community at the micro-habitat scale. Soils were physically fractionated into particle size fractions, free-particulate organic matter (F-POM), macro-aggregates (250–2000 μm) and micro-aggregates (53–250 μm). Organic C was enriched in silt and clay, micro-aggregates and F-POM fractions. Enzymes showed the greatest activity in the fine fractions (silt and clay) and F-POM, and were largely influenced by organic C content. MicroResp-CLPP (Community Level Physiological Profile) showed the lowest catabolic responses in the sand and the highest in the fine fraction and micro-aggregates. In general, organic C availability drove soil activity and functional diversity: soils with the higher amount of organic C showed the higher catabolic activity. However, this response was variable within soil fractions, where organic C accessibility, as well as microbial selection and distribution, affected functional diversity.