Dynamics of 13C‐labeled mustard litter (Sinapis alba) in particle‐size and aggregate fractions in an agricultural cropland with high‐ and low‐yield areas

The application of ¹³C‐labeled litter enables to study decomposition processes as well as the allocation of litter‐derived carbon to different soil C pools. ¹³Carbon‐labeled mustard litter was used in order to compare decomposition processes in an agricultural cropland with high‐yield (HY) and low‐yield (LY) areas, the latter being characterized by a finer texture and a lower organic‐C (OC) content. After tracer application, ¹³C concentrations were monitored in topsoil samples in particulate organic matter (POM) and in fine mineral fractions (silt‐ and clay‐sized fractions). After 568 d, approximately 5% and 10% of the initial ¹³C amount were found in POM fractions of LY and HY areas, respectively. Higher amounts were found in POM occluded in aggregates than in free POM. Medium‐term (0.5–2 y) storage of the initial ¹³C in fine silt‐ and clay‐sized fractions amounts to 10% in HY and LY soils, with faster enrichment but also faster disappearance of the ¹³C signal from LY soils. Amounts of 80%–90% of the added ¹³C were mineralized or leached in the observed period. Decomposition of free POM was faster in HY than in LY areas during the first year, but the remaining ¹³C amounts in occluded‐POM fractions were higher in HY soils after 568 d. High‐yield and low‐yield areas showed different ¹³C dynamics in fine mineral fractions. In LY soils, ¹³C amounts and concentrations in mineral‐associated fractions increased within 160 d after application and decreased in the following time period. In HY areas, a significant increase in ¹³C amounts did not occur until after 568 d. The results indicate initially faster decomposition processes in HY than in LY areas due to different soil conditions, such as soil texture and water regime. The higher silt and clay contents of LY areas seem to promote a faster aggregate formation and turnover, leading to a closer contact between POM and mineral surfaces in this area. This favors the OC storage in fine mineral fractions in the medium term. Lower aggregate formation and turnover in the coarser textured HY soil leads to a delayed C stabilization in silt‐ and clay‐sized fractions.     

Black carbon in the zonal steppe soils of Russia

Black Mollisols are typically rich in charred organic matter, however, little is known about the zonal distribution of black C (BC) in steppe soils. In this study, we used benzene polycarboxylic acids (BPCA) as specific markers for BC in particle‐size fractions of depth profiles in several zonal soils (Greyzem, Phaeozem, Chernozem, Kastanozem) of the Russian steppe. In addition, liquid‐state ¹³C‐NMR spectra were obtained on the alkaline‐soluble soil organic matter (SOM). The results showed that both the content and depth distribution of BC varies in the different soil types; the concentration of BC in the bulk top soils being closely related to the aromaticity of the SOM (r² = 0.98 for the native topsoils, 0.83 for top‐ and subsurface soils). Especially the Chernozems were rich in aromatic SOM, which partly contained more than 17% BC of total C, most of which being allocated in the mineral fractions. Long‐term arable cropping did not reduce the BC contents of the surface soil, though it did promote the enrichment of BC in the silt fractions. The same shift was detected as soil depth increased. We conclude that BC is not fully inert in these soils, but apparently can be preserved in the silt as decomposition of SOM increased, i.e., it accumulates exactly in that fraction, which has been formerly assigned to contain old, aromatic C.     

Is thermal oxidation at different temperatures suitable to isolate soil organic carbon fractions with different turnover?

Findings of previous studies suggest that there are relations between thermal stability of soil organic matter (SOM), organo‐mineral associations, and stability of SOM against microbial decay. We aimed to test whether thermal oxidation at various temperatures (200°C, 225°C, 275°C, 300°C, 400°C, or 500°C) is capable of isolating SOM fractions with increasing stability against microbial degradation. The investigation was carried out on soils (Phaeozem and Luvisol) under different land‐use regimes (field, grassland, forest). The stability of the obtained soil organic carbon (SOC) fractions was determined using the natural‐¹³C approach for continuously maize‐cropped soils and radiocarbon dating. In the Luvisol, thermal oxidation with increasing temperatures did not yield residual SOC fractions of increasing microbial stability. Even the SOC fraction resistant to thermal oxidation at 300°C contained considerable amounts of young, maize‐derived C. In the Phaeozem, the mean ¹⁴C age increased considerably (from 3473 y BP in the mineral‐associated SOC fraction to 9116 y BP in the residual SOC fraction after thermal oxidation at 300°C). An increasing proportion of fossil C (calculated based on ¹⁴C data) in residual SOC fractions after thermal oxidation with increasing temperatures indicated that this was mainly due to the relative accumulation of thermally stable fossil C. We conclude that thermal oxidation with increasing temperature was not generally suitable to isolate mineral‐associated SOC fractions of increasing microbial stability.     

Long‐term fertilization and manuring effects on physically separated soil organic‐matter pools under continuous wheat cropping at a rainfed semiarid site in China

An essential prerequisite for a sustainable soil use is to maintain a satisfactory soil organic‐matter (OM) level. This might be achieved by sound fertilization management, though impacts of fertilization on OM have been rarely investigated with the aid of physical fractionation techniques in semiarid regions. This study aimed at examining changes in organic C (OC) and N concentrations of physically separated soil OM pools after 26 y of fertilization at a site of the semiarid Loess Plateau in China. To separate sensitive OM pools, total macro‐OM (> 0.05 mm) was obtained from bulk soil by wet‐sieving and then separated into light macro‐OM (< 1.8 g cm^–3) and heavy macro‐OM (> 1.8 g cm^–3) subfractions; bulk soil was also differentiated into light OM (< 1.8 g cm^–3) and mineral‐associated OM (> 1.8 g cm^–3). Farmyard manure increased concentrations of total macro‐OC and N by 19% and 25%, and those of light fraction OC and N by 36% and 46%, compared to no manuring; both light OC and N concentrations but only total macro‐OC concentration responded positively to mineral fertilizations compared to no mineral fertilization. This demonstrated that the light‐fraction OM was more sensitive to organic or inorganic fertilization than the total macro‐OM. Mineral‐associated OC and N concentrations also increased by manuring or mineral fertilizations, indicating an increase of stable OM relative to no fertilization treatment, however, their shares on bulk soil OC and N decreased. Mineral fertilizations improved soil OM quality by decreasing C : N ratio in the light OM fraction whereas manuring led to a decline of the C : N ratio in the total macro‐OM fraction, with respect to nil treatment. Further fractionation of the total macro‐OM according to density clarified that across treatments about 3/4 of total macro‐OM was associated with minerals. Thus, by simultaneously applying particle‐size and density separation procedures, we clearly demonstrated that the macro‐OM differed from the light OM fraction not only in its chemical composition but also in associations with minerals. The proportion of the 0.5–0.25 mm water‐stable aggregates of soil was higher under organic or inorganic fertilizations than under no manure or no mineral fertilization, and increases in OC and N concentrations of water‐stable aggregates as affected by fertilization were greater for 1–0.5 and 0.5–0.25 mm classes than for the other classes. Results indicate that OM stocks in different soil pools can be increased and the loose aggregation of these strongly eroded loess soils can be improved by organic or inorganic fertilization.     

Soil‐organic‐matter stability in sandy cropland soils is related to land‐use history

Sandy cropland soils in NW Europe were found to contain unusually high organic‐carbon (OC) levels, and a link with their land‐use history has been suggested. This study's aim was to assess the discriminating power of physical and chemical fractionation procedures to yield information on soil‐organic‐matter (OM) stability for these soils. In relict‐ and cultivated‐heathland soils, much higher proportions of 6% NaOCl treatment–resistant but 10% HF–soluble OC (MOC) and N (32.2% and 29.9%) were measured compared to a set of “permanent"‐cropland soils without a history of heathland land use (11.9% and 8.5%). Also, the proportions of 6% NaOCl– and 10% HF treatment–resistant OC and N in the relict and cultivated heathlands (19.2% and 12.0%) were higher than in the permanent‐cropland soils (17.7% and 5.7%). Stepwise multiple linear‐regression yielded a significant relationship between the annual mineralization (g C [100 g OC]^–1), soil OC (g C kg^–1) content, and %MOC: Annual mineralization = 4.347 – 0.087 soil OC – 0.032 %MOC (R² = 0.65). Combinations of incubation experiments for quantification of the labile soil OM pool with chemical fractionation may thus yield meaningful data for development of soil‐organic‐matter models with measurable pools, but their applicability will be limited to specific combinations of former land use with soil, climate, and current management.     

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.     

Soil organic carbon and nitrogen fractions and water‐stable aggregation as affected by cropping and grassland reclamation in an arid sub‐alpine soil

This paper investigates effects of cropping abandonment and perennial grass growing on soil organic C and N pools and aggregate stability, by comparing soils under native grassland, crop cultivation, perennial grass growing and cropping abandonment, in degraded cropland at a sub‐alpine site in north‐western China. The pools of total and particulate organic C (115 and 37 Mg ha⁻¹) in the 0–30 cm soil layer of native grassland were reduced by 31 and 54% after 30 years of crop cultivation. After 4 years of conversion from cropland to perennial grass growing total and particulate organic C pools were increased by 29 and 56%, whereas 4 year cropping abandonment increased particulate organic C by 36%. Rapid increases in total and particulate N were also found in perennial grass growing and cropping abandonment soils. The native grassland soil and soils of cropping abandonment and perennial grass growing had higher carbohydrate C concentrations in the 0–10 cm layer than the cropped soil. The rapid recovery of particulate organic fraction and carbohydrates in the re‐vegetated soils were probably due to higher plant biomass inputs and lower organic matter decomposition compared with those in the cropped soil. Aggregate stability of the 0–30 cm soil layer was significantly decreased by crop cultivation but showed a good recovery after 4 year re‐vegetations. This study suggests that reduction of soil organic matter and aggregate stability under crop cultivation may be remedied by cropping abandonment or perennial grass growing. Copyright © 2008 John Wiley & Sons, Ltd.     

A comparison of two methods for the isolation of free and occluded particulate organic matter

Various methods exist for the isolation of particulate organic matter (POM), one of the soil‐organic‐matter (SOM) fractions reacting most sensitive on land‐use or soil‐management changes. A combination of density separation and ultrasonic treatment allows to isolate two types of POM: (1) free POM and (2) POM occluded in soil aggregates. POM fractions are closely linked to their biochemical function for the formation and stabilization of aggregates, therefore methods using different aggregate sizes may result in different POM fractions isolated. We evaluated two physical fractionation procedures to reveal whether they yield different POM fractions with respect to amount and composition, using grassland and arable soils with sandy‐loam to sandy–clay‐loam texture and thus low macroaggregate stability. Method I used air‐dried aggregates of <2.0 mm size and a low‐energy sonication for aggregate disruption, method II used field‐moist aggregates <6.3 mm and a high‐energy–sonication procedure for aggregate disruption. POM fractions were analyzed by elemental analysis (C, N) and CPMAS ¹³C‐NMR spectroscopy. With both methods, about similar proportions of the SOM are isolated as free or occluded POM, respectively. The free‐ and occluded‐POM fractions obtained with method I are also rather similar in C and N concentration and composition as shown by ¹³C‐NMR spectroscopy. Method II isolates a free‐ and occluded‐POM fraction with significantly different C and N concentrations. NMR spectra revealed significant differences in the chemical composition of both fractions from method II, with the occluded POM having lower amounts of O‐alkyl C and higher amounts of aryl C and alkyl C than the free POM. Due to the use of larger, field‐moist aggregates with minimized sample pretreatment, two distinctly different POM fractions are isolated with method II, likely to be more closely linked to their biochemical function for the formation and stabilization of aggregates. High‐energy sonication as in method II also disrupts small microaggregates <63 µm and releases fine intraaggregate POM. This fraction seems to be a significant component of occluded POM, that allows a differentiation between free and occluded POM in sandy soils with significant microaggregation. It can be concluded, that microaggregation in arable soils with sandy texture is responsible for the storage of a more degraded occluded POM, that conversely supports the stabilization of fine microaggregates.     

Organo‐mineral associations in temperate soils: Integrating biology,mineralogy, and organic matter chemistry

We summarize progress with respect to (1) different approaches to isolate, extract, and quantify organo‐mineral compounds from soils, (2) types of mineral surfaces and associated interactions, (3) the distribution and function of soil biota at organo‐mineral surfaces, (4) the distribution and content of organo‐mineral associations, and (5) the factors controlling the turnover of organic matter (OM) in organo‐mineral associations from temperate soils. Physical fractionation achieves a rough separation between plant residues and mineral‐associated OM, which makes density or particle‐size fractionation a useful pretreatment for further differentiation of functional fractions. A part of the OM in organo‐mineral associations resists different chemical treatments, but the data obtained cannot readily be compared among each other, and more research is necessary on the processes underlying resistance to treatments for certain OM components. Studies using physical‐fractionation procedures followed by soil‐microbiological analyses revealed that organo‐mineral associations spatially isolate C sources from soil biota, making quantity and quality of OM in microhabitats an important factor controlling community composition. The distribution and activity of soil microorganisms at organo‐mineral surfaces can additionally be modified by faunal activities. Composition of OM in organo‐mineral associations is highly variable, with loamy soils having generally a higher contribution of polysaccharides, whereas mineral‐associated OM in sandy soils is often more aliphatic. Though highly reactive towards Fe oxide surfaces, lignin and phenolic components are usually depleted in organo‐mineral associations. Charred OM associated with the mineral surface contributes to a higher aromaticity in heavy fractions. The relative proportion of OC bound in organo‐mineral fractions increases with soil depth. Likewise does the strength of the bonding. Organic molecules sorbed to the mineral surfaces or precipitated by Al are effectively stabilized, indicated by reduced susceptibility towards oxidative attack, higher thermal stability, and lower bioavailability. At higher surface loading, organic C is much better bioavailable, also indicated by little ¹⁴C age. In the subsurface horizons of the soils investigated in this study, Fe oxides seem to be the most important sorbents, whereas phyllosilicate surfaces may be comparatively more important in topsoils. Specific surface area of soil minerals is not always a good predictor for C‐stabilization potentials because surface coverage is discontinuous. Recalcitrance and accessibility/aggregation seem to determine the turnover dynamics in fast and intermediate cycling OM pools, but for long‐term OC preservation the interactions with mineral surfaces, and especially with Fe oxide surfaces, are a major control in all soils investigated here.     

How relevant is recalcitrance for the stabilization of organic matter in soils?

Traditionally, the selective preservation of certain recalcitrant organic compounds and the formation of recalcitrant humic substances have been regarded as an important mechanism for soil organic matter (SOM) stabilization. Based on a critical overview of available methods and on results from a cooperative research program, this paper evaluates how relevant recalcitrance is for the long‐term stabilization of SOM or its fractions. Methodologically, recalcitrance is difficult to assess, since the persistence of certain SOM fractions or specific compounds may also be caused by other stabilization mechanisms, such as physical protection or chemical interactions with mineral surfaces. If only free particulate SOM obtained from density fractionation is considered, it rarely reaches ages exceeding 50 y. Older light particles have often been identified as charred plant residues or as fossil C. The degradability of the readily bioavailable dissolved or water‐extractable OM fraction is often negatively correlated with its content in aromatic compounds, which therefore has been associated with recalcitrance. But in subsoils, dissolved organic matter aromaticity and biodegradability both are very low, indicating that other factors or compounds limit its degradation. Among the investigated specific compounds, lignin, lipids, and their derivatives have mean turnover times faster or similar as that of bulk SOM. Only a small fraction of the lignin inputs seems to persist in soils and is mainly found in the fine textural size fraction (<20 µm), indicating physico‐chemical stabilization. Compound‐specific analysis of ¹³C : ¹²C ratios of SOM pyrolysis products in soils with C3‐C4 crop changes revealed no compounds with mean residence times of > 40–50 y, unless fossil C was present in substantial amounts, as at a site exposed to lignite inputs in the past. Here, turnover of pyrolysis products seemed to be much longer, even for those attributed to carbohydrates or proteins. Apparently, fossil C from lignite coal is also utilized by soil organisms, which is further evidenced by low ¹⁴C concentrations in microbial phospholipid fatty acids from this site. Also, black C from charred plant materials was susceptible to microbial degradation in a short‐term (60 d) and a long‐term (2 y) incubation experiment. This degradation was enhanced, when glucose was supplied as an easily available microbial substrate. Similarly, SOM mineralization in many soils generally increased after addition of carbohydrates, amino acids, or simple organic acids, thus indicating that stability may also be caused by substrate limitations. It is concluded that the presented results do not provide much evidence that the selective preservation of recalcitrant primary biogenic compounds is a major SOM‐stabilization mechanism. Old SOM fractions with slow turnover rates were generally only found in association with soil minerals. The only not mineral‐associated SOM components that may be persistent in soils appear to be black and fossil C.     

Density fractionation of organic matter in dolomite‐derived soils

Dolomite (CaMg(CO₃)₂) constitutes half of the global carbonates. Thus, many calcareous soils have been developing rather from dolomitic rocks than from calcite (CaCO₃)‐dominated limestone. We developed a physical fractionation procedure based on three fractionation steps, using sonication with subsequent density fractionation to separate soil organic matter (SOM) from dolomite‐derived soil constituents. The method avoids acidic pretreatment for destruction of carbonates but aims at separating out carbonate minerals according to density. The fractionation was tested on three soils developed on dolostone parent material (alluvial gravel and solid rock), differing in organic‐C (OC) and inorganic‐C (IC) concentrations and degree of carbonate weathering. Soil samples were suspended and centrifuged in Na‐polytungstate (SPT) solutions of increasing density, resulting in five different fractions: two light fractions < 1.8 g cm^–3 (> 20 μm and < 20 μm), rich in OC and free of carbonate, and two organomineral fractions (1.8–2.4 g cm^–3 and 2.4–2.6 g cm^–3), containing 66–145 mg g^–1 and 16–29 mg g^–1 OC. The organomineral fractions consist of residual clay from carbonate weathering such as clay minerals and iron oxides associated with SOM. The fifth fraction (> 2.6 g cm^–3) was dominated by dolomite (85%–95%). The density separation yielded fractions differing in mineral compositions, as well as in SOM, indicated by soil‐type‐specific OC distributions and decreasing OC : N ratios with increasing density of fractions. The presented method is applicable to a wide range of dolomitic and most likely to all other calcareous soils.     

Stabilization of organic matter by soil minerals — investigations of density and particle‐size fractions from two acid forest soils

We tested the hypothesis whether organic matter in subsoils is a large contributor to organic carbon (OC) in terrestrial ecosystems and if survival of organic matter in subsoils is the result of an association with the soil mineral matrix. We approached this by analyzing two forest soil profiles, a Haplic Podzol and a Dystric Cambisol, for the depth distribution of OC, its distribution among density and particle‐size fractions, and the extractability of OC after destruction of the mineral phase by treatment with hydrofluoric acid (HF). The results were related to indicators of the soil mineralogy and the specific surface area. Finally, scanning electron microscopy combined with energy dispersive X‐ray spectroscopy (SEM‐EDX) was used to visualize the location of OC at mineral surfaces and associations with elements of mineral phases. The subsoils (B and C horizons) contained 40—50% of the soil OC including the organic forest floor layers. With increasing depth of soil profiles (1) the radiocarbon ages increased, and (2) increasing portions of OC were either HF‐soluble, or located in the density fraction d >1.6 g cm^—3, or in the clay fraction. The proportions of OC in the density fraction d >1.6 g cm^—3 were closely correlated to the contents of oxalate and dithionite‐citrate‐bicarbonate‐extractable Fe (r² = 0.93 and 0.88, P <0.001). SEM‐EDX analyses suggested associations of OC with aluminum whereas silicon‐enriched regions were poor in OC. The specific surface area and the microporosity of the soil mineral matrix after destruction of organic matter were less closely correlated to OC than the extractable iron fractions. This is possibly due to variable surface loadings, depending on different OC inputs with depth. Our results imply that subsoils are important for the storage of OC in terrestrial ecosystems because of intimate association of organic matter with secondary hydrous aluminum and iron phases leading to stabilization against biological degradation.     

Soil Organic Carbon and Nitrogen Fractions in Temperate Alley Cropping Systems

Abstract

Alley cropping may promote greater sequestration of soil organic carbon. The objective of this study was to examine spatial variability of soil organic carbon (C) and nitrogen (N) fractions relative to tree rows in established alley cropping systems in north central Missouri. Soils were collected to a depth of 30 cm from two alley cropped sites, a 19‐yr‐old pecan (Carya illinoinensis)/bluegrass (Poa trivialis) intercrop (pecan site) and an 11‐yr‐old silver maple (Acer saccharinum)/soybean (Glycine max)–maize (Zea mays) rotation (maple site). Particulate organic matter (POM) C constituted 15–65% and 14–41% of total organic C (TOC) at the pecan and maple sites respectively, whereas POM N comprised 3 to 24% of total N (TKN). TOC and TKN were on average 13% and 18% higher at the tree row than at the middle of the alley for surface soils (0–10 cm) at the pecan site, respectively. Similarly, POM C was two to three times higher at the tree row than the alley for subsurface soils at the maple site. No differences in microbial biomass C and N between positions were observed. Observed results suggest the existence of spatially dependent patterns for POM C, TOC, and TKN, relative to tree rows in alley cropping.     

Soil organic matter composition and soil lightness

Relationships between soil lightness, soil organic matter (SOM) composition, content of organic C, CaCO₃, and texture were studied using 42 top‐soil horizons from different soil types located in southern Germany. SOM composition was determined by CPMAS ¹³C NMR spectroscopy, soil color was measured by diffuse‐reflectance spectrophotometry and given in the CIE L*a*b* color coordination system (Commission Internationale de l'Eclairage, 1978). Multiple‐regression analysis showed, that soil lightness of top‐soil horizons is principally determined by OC concentration, but CaCO₃ and soil texture are also major variables. Soil lightness decreased with increasing OC content. Carbonate content had an important effect on soil lightness even at low concentrations due to its lightening property. Regressions between soil lightness and organic C content were strongly linear, when the soils were differentiated according to texture and CaCO₃ content. The aryl‐C content was the only SOM component which correlated significantly with soil lightness (r_S = –0.87). In the linear regressions carried out on the different soil groups, soil aryl‐C content was a more significant predictor for soil lightness than total OC content.     

Beziehungen zwischen Klimafaktoren und C-, N-Pools in Partikelgrößen-Fraktionen zonaler Steppenböden Rußlands

Relationships between climatic factors and C, N pools in particle-size fractions of steppe soils, Russia Many soils of the Russian steppe are characterized by high soil organic matter contents and similar parent material. Thus, they are suitable for investigations of a climatic impact on C and N pools. We sampled 10 topsoils of the zonal Russian steppe at 0–10 and about 50–60 cm depth intervals. After particle-size fractionation into clay (<2 μm), silt (2–20 μm), fine sand (20–250 μm) organic C and N concentrations were determined in bulk soils and fractions. The results suggest that especially the older organic matter of the subsoil (in the silt fraction) is correlated with climatic factors. Topsoils show less evidence for climatic influences on C and N pools. As the ratio of mean annual precipitation to potential evaporation (=N/V) increases, C/N ratios decrease in all fractions and, thus, in the bulk subsoil. Obviously the degree of soil organic matter alteration was more pronounced in the order Greyzem (N/V = 1.0) > Chernozem, Phaeozem (N/V = 0.89) > Haplic Kastanozem (N/V = 0.6) > Calcic (N/V = 0.34), and Gypsic Kastanozem (N/V = 0.32). The organic carbon contents of the bulk subsoil are highest in the subsoil of the Chernozem and Phaeozem, and decrease with increasing N/V ratio (i.e., increasing heat input and dryness) to the Calcic Kastanozem. This is accompanied by an increasing enrichment of organic carbon in the silt fractions (r = ?0.99 for the correlation of the C enrichment in silt with N/V).     

Integrated Soil Fertility Management: Aggregate carbon and nitrogen stabilization in differently textured tropical soils

Soil organic matter is important to improve and sustain soil fertility in tropical agroecosystems. The combined use of organic residue and fertilizer inputs is advocated for its positive effects on short-term nutrient supply, but the effect of the integrated use on long-term stabilization of soil organic C and N is still unclear. We conducted a 1.5-y soil incubation experiment with maize (Zea mays) residue and urea fertilizer to examine the stabilization of C and N in four Sub-Saharan African soils differing in texture (sand, sandy loam, clay loam, and clay). The inputs were enriched with ¹³C and ¹⁵N in a mirror-labelling design to trace the fate of residue-C and N, and fertilizer-N in combination. We hypothesized that combining inputs would enhance the stabilization of C and N relative to either input alone across a range of soil textures. The treatments were destructively sampled after 0.25, 0.5, and 1.5 y to assess input-derived C and N stabilization in soil macro- and microaggregate fractions. The combination treatment had a significant but small (2% of residue-applied C) increase in residue-C stabilized in the total soil after 0.25 y, but this increase did not persist after 0.5 and 1.5 y. While combining residue and fertilizer decreased the amount of residue-N stabilized within 53- to 2000-μm sized soil aggregates (e.g., 7% less at 1.5 y), it increased the stabilization of fertilizer-N at all sampling times (e.g., 20% more at 1.5 y). The increased amount of fertilizer-N stabilized was significantly greater than the amount of residue-N lost in the combined input treatments in the three finer textured soils at 1.5 y, indicating an interactive increase in the stabilization of new N. Our results indicate that combining residue with fertilizer inputs can increase the short-term stabilization of N, which has the potential to improve soil fertility. However, benefits to N stabilization from combining organic residues and fertilizer seem to be less in coarser-textured soils.     

Nitrogen mineralization and nitrogen uptake by maize as influenced by light and heavy organic matter fractions

On a sandy tropical soil, organic materials (prunings of Leucaena leucocephala, Senna siamea and maize stover) with contrasting C/N ratio (13, 18 and 56, respectively) were applied at the rate of 15 t ha^?1a^?1 in order to increase the amount of soil organic matter. Two light fractions (LF1 = LF > 2 mm and LF2 = 0.25 mm < LF < 2 mm) and the heavy fraction (HF) of the soil organic matter pool were determined by means of a combined density/particle size fractionation procedure and data obtained were related to soil nitrogen mineralization under controlled conditions and to nitrogen uptake by maize under field conditions. Under controlled conditions and when the LF1 fraction was excluded, nitrogen mineralization was found not to be correlated to total organic carbon content in the soil (R²=0.02). The R²-value of the linear regression increased considerably, when amount and C/N ratio of the LF2 fraction was taken into account in the regression analysis (R² = 0.88). Under field conditions, a multiple linear regression with amount and C/N ratio of HF, LF1 and LF2 better explained variation in crop nitrogen content and nitrogen uptake of maize (R² = 0.78 and 0.94) than a simple linear regression with total organic carbon (R² = 0.48 and 0.76). The results illustrate the importance of the two light and heavy organic matter fractions for estimating soil nitrogen mineralization. Determination of light and heavy soil organic matter fractions by density/particle size fractionation seems to be a promising tool to characterize functional pools of soil organic matter.     

Labile and stable pools of organic matter in soil amended with sewage sludge biochar

One of the main advantages of using biochar for agricultural purposes is its ability to store carbon (C) in soil for a long-term. Studies of labile and stable fractions of soil organic matter (SOM) may be a good indicator of the dynamics of biochar in soils. This study evaluated the effects of applying sewage sludge biochar (SSB) in combination with mineral fertilizer on fractions of SOM. To conduct this evaluation, 15 Mg ha^?1 of SSB combined or not with mineral fertilizer (NPK) was applied to the soil in two cropping seasons. Apart from total organic C (TOC), the labile and stable fractions of SOM were also determined. The combined use of SSB and NPK resulted in higher TOC, a 22% to 40% increase compared to the control and to the NPK treatments, respectively. The SSB produced at a lower temperature increased the labile fractions of SOM, especially the microbial biomass C, showing its capacity to supply nutrients in the short-term. The stable pools of SOM are increased after adding SSB produced at a higher temperature. It was concluded that pyrolysis temperature is a key-factor that determines the potential of SSB to accumulate C in labile and stable fractions of SOM.     

Organic C levels in intensively managed arable soils – long-term regional trends and characterization of fractions

Substantial losses of soil organic carbon (SOC) from the plough layer of intensively managed arable soils in western Europe have recently been reported, but these estimates are associated with very large uncertainties. Following soil surveys in 1952 and 1990 of arable soils in West Flanders (Belgium), we resampled 116 sites in 2003 and thus obtained three paired measurements of the OC stocks in these soils. Ten soils were selected for detailed physical fractionation to obtain possible further explanations for changes in SOC stocks. Between 1990 and 2003, the SOC stocks decreased at an average rate of ?0.19 t OC ha^?1 year^?1. This loss is significant but is still less than half the rate of SOC decrease that was estimated previously for the whole region of Flanders, which includes the study area. Variation in SOC stocks or in the magnitude of SOC stock losses could not be related to soil texture, to changes in ploughing depth, or to recent land‐use changes. A good relationship, however, was found between the SOC losses and organic matter (OM) inputs. The results of the physical fractionation also suggested management to be the predominant factor determining variation in SOC stocks because no correlation was found between soil texture and the absolute amounts of OC present in the largest OM fractions, that is, the OC in free particulate organic matter (POM), and OC associated with the silt + clay size fraction. The proportion of OC in free POM was up to 40% of the total OC, which indicates the important impact of management on SOC and also indicates that a substantial part of the SOC still present, may in the future be lost at a time scale of years to decades assuming that the intensive management continues.     

Repeated monitoring of organic carbon stocks after eight years reveals carbon losses from intensively managed agricultural soils in Western Germany

Past land‐use changes, intensive cropping with large proportions of root crops, and preferred use of mineral fertilizer have been made responsible for proceeding losses of soil organic C (SOC) in the plough layer. We hypothesized that in intensive agriculturally managed regions changes in SOC stocks would be detectable within a decade. To test this hypothesis, we tracked the temporal development of the concentrations and stocks of SOC in 268 arable sites, sampled by horizon down to 60 cm in the Cologne‐Bonn region, W Germany, in 2005 and in 2013. We then related these changes to soil management data and humus balances obtained from farmers' surveys. As we expected that changes in SOC concentrations might at least in part be minor, we fractionated soils from 38 representative sites according to particle size in order to obtain C pools of different stability. We found that SOC concentrations had increased significantly in the topsoil (from 9.4 g kg^?1 in 2005 to 9.8 g kg^?1 in 2013), but had decreased significantly in the subsoil (from 4.1 g kg^?1 in 2005 to 3.5 g kg^?­1 in 2013). Intriguingly, these changes were due to changes in mineral‐bound SOC rather than to changes in sand‐sized organic matter pools. As bulk density decreased, the overall SOC stocks in the upper 60 cm exhibited a SOC loss of nearly 0.6 t C (ha · y)^?1 after correction by the equivalent soil mass method. This loss was most pronounced for sandy soils [?0.73 t SOC (ha · y)^?1], and less pronounced for loamy soils [?0.64 t SOC (ha · y)^?1]; silty soils revealed the smallest reduction in SOC [?0.3 t SOC (ha · y)^?1]. Losses of SOC occurred even with the overall humus balances having increased positively from about 20 kg C (ha · y)^?1 (2003–2005) to about 133 kg C (ha · y)^?1 (2005–2013) due to an improved organic fertilization and intercropping. We conclude that current management may fail to raise overall SOC stocks. In our study area SOC stocks even continued to decline, despite humus conservation practice, likely because past land use conversions (before 2005) still affect SOC dynamics.