A re‐evaluation of the enriched labile soil organic matter fraction

Identifying ‘functional' pools of soil organic matter and understanding their response to tillage remains elusive. We have studied the effect of tillage on the enriched labile fraction, thought to derive from microbes and having an intermediate turnover time. Four soils, each under three regimes, long‐term arable use without tillage (NT), long‐term arable under conventional tillage (CT), and native vegetation (NV), were separated into four aggregate size classes. Particle size fractions of macro‐ (250–2000 μm) and microaggregates (53–250 μm) were isolated by sonication and sieving. Subsequently, densiometric and chemical analyses were made on fine‐silt‐sized (2–20 μm) particles to isolate and identify the enriched labile fraction. Across soils, the amounts of C and N in the particle size fractions were highly variable and were strongly influenced by mineralogy, specifically by the contents of Fe and Al oxides. This evidence indicates that the fractionation procedure cannot be standardized across soils. In one soil, C associated with fine‐silt‐sized particles derived from macroaggregates was 567 g C m^?2 under NV, 541 g C m^?2 under NT, and 135 g C m^?2 under CT, whereas C associated with fine‐silt‐sized particles derived from microaggregates was 552, 1018, 1302 g C m^?2 in NV, NT and CT, respectively. These and other data indicate that carbon associated with fine‐silt‐sized particles is not significantly affected by tillage. Its location is simply shifted from macroaggregates to microaggregates with increasing tillage intensity. Natural abundance ¹³C analyses indicated that the enriched labile fraction was the oldest fraction isolated from both macro‐ and microaggregates. We conclude that the enriched labile fraction is a ‘passive' pool of soil organic matter in the soil and is not derived from microbes nor sensitive to cultivation.     

Organic matter in particle-size fractions from A and B horizons of a Haplic Alisol

The organic matter in soils may be stabilized by its interactions with minerals. We have studied such interactions in a Haplic Alisol under forest in which clay and organic matter have migrated from an eluvial A horizon to accumulate in an illuvial B horizon. We have tried to trace the fate of organic matter in these horizons (Ah and Bvt) by determining clay mineralogy, carbon and nitrogen content, hydrolysable amino acids, lignin signature by alkaline CuO oxidation and carbon species by ¹³C CPMAS NMR of bulk soils and particle‐size fractions. In both horizons, most of the organic matter was present in O–alkyl and methylene structures, each contributing one‐third to the bulk organic matter. In the Ah horizon the ratios of carbon‐to‐nitrogen, and yields for lignin and hydrolysable amino acids decreased as the particle‐size class decreased, but side‐chain oxidation of lignin compounds increased with decreasing particle size. In contrast to previous observations, the proportions of O–alkyl carbon increased as particle size decreased, constituting a major proportion of the organic carbon in the clay‐size fractions from both the Ah and Bvt horizons (≥ 38%), while proportions of methylene carbon decreased. Illite was the dominant mineral in the fraction ≤ 6 μm, whereas the mobile fine clay fraction (<0.2 μm) was rich in smectites – minerals with large surface areas. Our results support the hypothesis that potentially labile organic matter, such as O–alkyl carbon typically present in polysaccharides, may be stabilized against further degradation in organomineral complexes.     

Aggregate-occluded black carbon in soil

The great stability of black carbon (BC) in soils may not be solely attributable to its refractory structure but also to poor accessibility when physically enveloped by soil particles. Our aim was to elucidate the intensity of physical entrapment of BC within soil aggregates. For this purpose, the A horizon of a forest, and of a grassland soil, and of three soils under tillage, were sampled at the experimental station Rotthalmünster, Germany. Black carbon was assessed in water‐stable aggregates and aggregate‐density fractions using benzene polycarboxylic acids as specific markers. The greatest BC concentrations made up 7.2% of organic carbon and were found in the < 53 μm fraction. The smallest BC concentrations occurred in the large macroaggregate fractions (> 2 mm). This pattern has been sustained even after tillage. The C‐normalized BC concentrations were significantly greater (P < 0.05) in the occluded particulate organic matter (OPOM) fractions than in the free particulate organic matter (FPOM) and the mineral fractions. This enrichment of BC compared with organic carbon in the OPOM fractions amounted to factors of 1.5–2.7. Hence, BC was embedded within microaggregates in preference to other organic carbon compounds. Only 2.5–3.5% of BC was located in the OPOM fraction < 1.6 g cm^?3, but 22–24% in the OPOM fraction with a density of 1.6–2.0 g cm^?3. This suggests that BC possibly acted as a binding agent or was selectively enriched during decomposition of protected SOM, or both. Physical inclusion, particularly within microaggregates, could therefore contribute to the long mean‐residence times of soil‐inherent BC.     

Land‐use effects on the distribution of soil organic carbon within particle‐size fractions of volcanic soils in the Transmexican Volcanic Belt (Mexico)

The aim of this study was to determine the effect of land‐use and forest cover depletion on the distribution of soil organic carbon (SOC) within particle‐size fractions in a volcanic soil. Emphasis was given to the thermal properties of soils. Six representative sites in Mexico were selected in an area dominated by Andosols: a grassland site, four forested sites with different levels of degradation and an agricultural site. Soils were fractionated using ultrasonic energy until complete dispersion was achieved. The particle‐size fractions were coarse sand, fine sand, silt, clay and particulate organic matter from the coarse sand sized fraction (POM‐CS) and fine sand (POM‐FS). Soil organic carbon decreased by 70% after forest conversion to cropland and long‐term cultivation; forest cover loss resulted in a decrease in SOC of up to 60%. The grassland soil contained 45% more SOC than the cropland one. Soil organic carbon was mainly associated with the silt‐size fraction; the most sensitive fractions to land‐use change and forest cover depletion were POM followed by SOC associated with the silt and clay‐sized fractions. Particulate organic matter can be used as an early indicator of SOC loss. The C lost from the clay and silt‐sized fractions was thermally labile; therefore, the SOC stored in the more degraded forest soils was more recalcitrant (thermally resistant). Only the transformation of forest to agricultural land produced a similar loss of thermally stable C associated with the silt‐sized fraction.     

Thermal oxidation does not fractionate soil organic carbon with differing biological stabilities

Thermal analysis techniques have been used to differentiate soil organic carbon (SOC) pools with differing thermal stability. A correlation between thermal and biological stability has been indicated in some studies, while others reported inconsistent relationships. Despite these controversial findings and no standardized method, several recently published studies used thermal analysis techniques to determine the biological stability and quality of SOC in mineral soils. This study examined whether thermal oxidation at temperature levels between 200°C and 400°C, combined with evolving gas analysis and isotope ratio mass spectrometry, is capable of identifying SOC pools with differing biological stability in mineral soils. Soil samples from three sites being under Miscanthus (C₄‐plant) cultivation for more than 17 years following former agricultural cropland (only C₃‐plant) cultivation were used. Due to natural shifts in ¹³C content, young and labile Miscanthus‐derived SOC could be distinguished from stable and old C₃‐plant‐derived SOC. The proportion of Miscanthus‐derived SOC increased significantly with increasing temperatures up to 350°C in bulk soil samples, indicating increasing oxidation of labile and young SOC with increasing temperatures. Use of density fractions to validate the thermally oxidized SOC from bulk soil samples revealed that the thermal oxidation patterns did not reflect the biological stability of SOC. The suggested biologically labile particulate organic carbon (light fraction from density fractionation) was clearly enriched in Miscanthus‐derived young SOC. The thermal oxidation patterns, however, revealed preferential oxidation of these biologically labile fractions not at low temperatures, but rather at higher temperatures. The reverse was found for the biologically stable mineral‐associated density fraction (heavy fraction). Based on different soil types, it was concluded that the thermal stability of SOC between 200°C and 400°C is not a suitable indicator of the biological stability of SOC and, thus, thermal oxidation is not capable of fractionating SOC pools with differing biological stability.     

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.     

Effect of soil pH on the chemical composition of organic matter in physically separated soil fractions in two broadleaf woodland sites at Rothamsted,UK

Although acid soils are common in forest ecosystems, and there is documented evidence of pH influencing transformations of organic matter in soil, there are surprisingly few studies on the influence of soil pH on the chemical structure of physically fractionated soil organic matter (SOM). The aim of this study was to characterize the influence of pH on the chemical and physical processes involved in SOM stabilization. Forest soils of different pH (4.4 and 7.8) sampled from two long‐term experiments at Rothamsted Research (UK) were physically fractionated. The free light fraction (FLF), the intra‐aggregate light fraction and the fine silt and clay (S + C, <25 µm) were characterized using elemental, isotopic (δ¹³C), thermogravimetric, differential thermal, diffuse reflectance infrared Fourier transform spectroscopy and high‐resolution magic angle spinning ¹H nuclear magnetic resonance analyses. The quantitative distribution of carbon (C) between SOM fractions differed between the two soils. Carbon contents in the light fractions from the acid soil were significantly greater than in those of the alkaline soil. In contrast, in S + C fractions, C content was greater in the alkaline soil. FLF from the acid soil was characterized by a greater C:N ratio, smaller δ¹³C and greater content of thermo‐labile compounds compared with FLF from the alkaline soil. In contrast, there was only a weak effect of soil pH on the chemical composition of the organic matter in S + C fractions. Irrespective of soil pH, these latter fractions contained mainly aliphatic compounds such as carbohydrates, carboxylic acid, amide and peptide derivates. This suggested that physical mechanisms, involving the interactions between SOM and mineral surfaces, are of greater importance than the presence of chemically recalcitrant species in protecting SOM associated with the finest soil fractions.     

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.     

Effect of straw amendment modes on soil organic carbon,nitrogen sequestration and crop yield on the North‐Central Plain of China

We quantified the effects of different straw return modes on soil organic carbon (SOC), total nitrogen content (TN) and C:N ratios in a wheat/maize double‐cropping agricultural system by analysing their content in different soil aggregate sizes and density fractions under four modes of straw return: (a) no return/retention of wheat and maize straw (Control); (b) retention of long wheat stubble only (Wheat Stubble); (c) retention of long wheat stubble and return of chopped maize straw (Mixed); and (d) return of chopped wheat and maize straw (Both Chopped). The Mixed and Both Chopped straw return modes produced the highest crop yields. Relative to the Control, SOC stock was 9.6% greater with the Mixed treatment and 14.5% greater with the Both Chopped treatment, whereas the Wheat Stubble treatment had no effect on SOC. Mixed and Both Chopped significantly enhanced TN stock relative to the Wheat Stubble and Control treatments. Compared with the Control, the Mixed and Both Chopped treatments increased the mass proportions of large macroaggregates and reduced the silt plus clay fraction; Mixed and Both Chopped caused a significant increase in SOC and TN in large and small macroaggregates; the Mixed treatment significantly increased SOC content in the coarse and fine intra‐aggregate particulate organic matter (iPOM) density fractions of large macroaggregates, whereas Both Chopped increased SOC in the coarse iPOM, fine iPOM and mineral‐associated organic matter (mSOM) density fractions of both large and small macroaggregates; and Mixed and Both Chopped enhanced TN content in coarse iPOM and fine iPOM within small macroaggregates. Although the Mixed treatment was slightly less effective at improving C sequestration in agricultural fields than the Both Chopped treatment, the Mixed treatment may nonetheless be the optimal plant residue management mode in terms of minimizing time and labour due to its ability to improve soil structure, maintain organic carbon levels and provide a means of sustainable crop production in intensive wheat/maize double‐cropping systems.     

Distribution of polycyclic aromatic hydrocarbons in particle‐size separates and density fractions of typical agricultural soils in the Yangtze River Delta,east China

Soil organic matter can be divided into different organic carbon (C) pools with different turnover rates. The organic pollutants in soils associated with these organic C pools may have different bioavailability and environmental risks during the decomposition of soil organic matter. We studied the distribution patterns of 15 USEPA priority polycyclic aromatic hydrocarbons (PAHs) in different particle‐size separates (clay, fine silt, coarse silt, fine sand and coarse sand) and density fractions (light and heavy fractions) of nine agricultural topsoils (0–20 cm depth) from a contaminated area in the Yangtze River Delta region of east China. There was a decreasing trend in PAH concentration in particle‐size separates with decreasing particle size. However, the different particle‐size separates had similar PAH composition. The concentration of PAHs in the light fraction ranged from 13 037 to 107 299 μg kg^?1, far higher than in the heavy fraction, which ranged from 222 to 298 μg kg^?1. Although the light fraction accounted for only 0.4–2.3% of the soils, it was associated with 31.5–69.5% of soil PAHs. The organic matter in coarse silt had the strongest capacity for enrichment with PAHs. Combining the distributions of PAHs and the turnover rates of organic matter in different soil fractions, the environmental risks of PAH‐polluted soils may be due mainly to the PAHs associated with sand and the light fraction.     

黑土颗粒有机碳和氮含量对有机肥剂量响应的定量关系

黑土是一种非常重要的耕种土壤,但是由于过度地开发利用和水土流失导致土壤有机质含量迅速下降,严重影响了耕地生产力和作物产量。为了能够快速恢复黑土肥力,利用海伦国家野外科学观测研究站内的长期定位试验,定量分析了黑土颗粒有机碳和氮含量对有机肥剂量的响应。田间试验开始于2001年,设置了4个施肥处理,分别为:1单施化肥(OM0);2低剂量有机肥与化肥配施(OM1);3中剂量有机肥与化肥配施(OM2);4高剂量有机肥与化肥配施(OM3)。在2011年播种前,采集各处理0~20 cm耕层土壤样品。应用有机碳物理分组方法,测定分析了土壤有机碳、氮及各组分的含量。研究结果表明长期不同剂量有机肥输入能够显著增加黑土总有机碳和全氮含量(P0.05),每增施1 t有机肥,土壤有机碳含量增加0.186 kg,土壤全氮含量增加0.02 kg,表明增加有机肥投入量是提高黑土有机碳含量的有效措施。有机肥的施用增加了土壤中粗颗粒和细颗粒组分,不同剂量有机肥处理表现为OM3OM2OM1OM0,而减小了土壤中矿质结合态组分的含量;随着有机肥施入量的增加,粗颗粒和细颗粒土壤有机碳和氮的含量呈增加的趋势,而矿质结合态中的有机碳含量则略有下降,表明粗颗粒和细颗粒有机碳和氮是黑土有机碳和氮的主要储存库,有机无机配施对土壤有机碳、氮的提升作用主要集中于对活性组分颗粒有机质的形成和积累。与OM0处理相比,有机肥的施入显著降低了颗粒有机质和矿质结合态有机质的C/N,并且随着有机肥施入量的增加而逐渐降低。与单施化肥相比,化肥有机肥配施能够显著增加土壤的总有机碳,全氮,颗粒有机碳、氮含量,其中以化肥配施高剂量有机肥效果最佳,有利于黑土土壤肥力的快速提升,改善黑土的土壤质量。     

Addition of Leucaena-KX2 mulch in a shaded coffee agroforestry system increases both stable and labile soil C fractions

Agroforestry systems have the potential to increase sequestration of atmospheric carbon dioxide (CO₂) as soil organic carbon (SOC) because of the increased rates of organic matter addition and retention. However, few studies have characterized the relative stability of sequestered SOC in soil. We characterized SOC storage in aggregate size and chemical stability classes to estimate the relative stability of SOC pools after the addition of Leucaena-KX2 pruning residues (mulch) from 2006 to 2008 in a shaded coffee agroforestry system in Hawaii. Soil samples were separated by microaggregate isolation, density flotation and dispersion, and acid hydrolysis, resulting in five distinct fractions that differed in relative stability: coarse particulate organic matter (POM), fine POM, microaggregate-protected POM, silt + clay hydrolyzable soil organic matter (SOM), and silt + clay non-hydrolyzable SOM. With mulch addition, the fine POM fraction increased. There was also a shift in the proportion of SOC to more stable silt + clay fractions. In the absence of mulch there was no significant change in SOC fractions. Given that the turnover time of SOC in silt + clay fractions is on the order of decades to centuries, the potential benefits of active shade management and mulching compensate for the loss of C sequestration in tree biomass from pollarding.     

Post-fire mineral N allocation and stabilisation in soil particle size fractions in Mediterranean grassland and shrubland

In the Mediterranean region, long-term post-fire soil N dynamics may be relevant in the stabilisation of soil organic matter and N cycling in the plant-soil system. Post-fire recycling of N may be retained by the retention of N in physically and/or chemically protected fractions of soil organic matter. We studied the allocation of post-fire ¹⁵N-tracer among different soil organic matter fractions (coarse sand, fine sand, coarse silt and fine silt + clay) and ¹⁵N-tracer dynamics for 12 years after prescribed fires in three different Mediterranean plant communities (grassland, mixed shrub-grassland and shrubland). We selected 6 plots for each community and we set experimental fires. Directly after the fires, we applied ¹⁵NH₄⁺-N and we monitored the fate of ¹⁵N-tracer over a period of 12 years. For this purpose, we carried out a physical size fractionation and we analysed the biochemical recalcitrance of N and ¹⁵N by acid hydrolysis in the size fractions obtained. In both burned and unburned plots the finest soil particles (<20 μm) accounted for most soil N. Fire promoted N increases in the medium size fractions while the N pool in the finest and coarsest fractions did not change after the fires. Interestingly, ¹⁵N-tracer was quickly incorporated into fine fractions from which, in the case of plant communities free of legumes, it was remobilised in the following years. Fire did not promote changes in recalcitrant N, but shrubland showed marked decreases in N recalcitrance 6 years after the fires. Despite the fact that the primary effects on soil fractions were detected just after the fires, these persisted for 12 years post-fire. Newly incorporated ¹⁵N-tracer was less recalcitrant than total N and, surprisingly, fine fractions had very low recalcitrant ¹⁵N values, similar to the coarse fractions. Apparently, the N transformations in the finest fraction (<20 μm) were mainly regulated by the quality of the ¹⁵N compounds retained in the fraction.     

Decomposition of labelled roots and root-C and -N allocation between soil fractions in mountain grasslands

Given the high turnover of fine roots in mountain grasslands, knowledge of their decomposition rates and the capacity of mountain grassland soils to stabilize root-derived C are central to understand the role of these ecosystems as potential C sinks. Here we studied the decomposition of fine roots in mountain grasslands and estimated the rates at which root-C and -N incorporated into protected pools at two soil depths. For this purpose, we incubated standard ¹³C- and ¹⁵N-labelled wheat roots mixed with unlabelled soil at 5 and 20 cm depth in two mountain grassland sites. Particle size fractionation allowed the quantification of the labelled wheat root-C and -N allocated to each size fraction (coarse sand, fine sand and silt plus clay sized) as well as their incorporation rates into the finest fraction. Between 62% and 78% root-C remained in the soil after one year of field incubation, faster decomposition being registered at the warmest site. In the following two years, roots decomposed much more slowly. In contrast to reports in the literature, our results indicate that decay rates during the first year were highest in the deep layer. The incorporation of wheat root-derived organic matter into the silt plus clay size fraction was also much greater during the first year of decomposition than in the following two years and also slightly higher in the deep soil than in topsoil. The incorporation rates of root-¹³C and root-¹⁵N into this fraction also suggest that the wheat-derived organic matter associated with this fraction was N-enriched and less recalcitrant (i.e., less resistant to acid hydrolysis) than that recovered from the coarser fractions. Furthermore, recalcitrant organic matter incorporated much more slowly than labile organic matter did. We conclude that the conditions of the subalpine grassland subsoil are more favourable for root decomposition than the topsoil and that the organic matter that incorporates into the protected pool is characterised by a high N content and low biochemical recalcitrance.     

Does Particulate Organic Matter Fraction Meet the Criteria for a Model Soil Organic Matter Pool?

There is a well-recognized need for improved fractionation methods to partition soil organic matter into functional pools. Physical separation based on particle size is widely used, yielding particulate organic matter(POM, i.e., free or "uncomplexed" organic matter 50 μm) as the most labile fraction. To evaluate whether POM meets criteria for an ideal model pool, we examined whether it is:1) unique, i.e., found only in the 50 μm fraction and 2) homogeneous, rather than a composite of different subfractions. Following ultrasonic dispersion, sand( 50 μm) along with coarse(20–50 μm) and fine(5–20 μm) silt fractions were isolated from a silt loam soil under long-term pasture at Lincoln, New Zealand. The sand and silt fractions contained 20% and 21% of total soil C, respectively.We adopted a sequential density separation procedure using sodium polytungstate with density increasing step-wise from 1.7 to 2.4 g cm~(-3) to recover organic matter(light fractions) from the sand and silt fractions. Almost all(ca. 90%) the organic matter in the sand fraction and a large proportion(ca. 60%–70%) in the silt fractions was recovered by sequential density separation. The results suggested that POM is a composite of organo-mineral complexes with varying proportions of organic and mineral materials. Part of the organic matter associated with the silt fractions shared features in common with POM. In a laboratory bio-assay, biodegradability of POM varied depending on land use(pasture arable cropping). We concluded that POM is neither homogeneous nor unique.     

Density separation of soil organic matter across three land uses in calcareous soils of Iran

ABSTRACT

The aim of this study was to examine the usefulness of physical and chemical fractionation in quantifying soil organic matter (SOM) in different stabilized fraction pools. Soil samples from three land use types in Lorestan province, Southwest Iran were examined to account for the amount of organic carbon and nitrogen in different SOM fractions. Size/density separation and chemical oxidation methods were applied to separate the SOM fractions including particulate organic matter (POM), Si + C (silt and clay), DOC (dissolved organic C), rSOM (oxidation-resistant organic carbon and nitrogen) and S + SA (sand and stable aggregates). The values obtained for TOC, TN, and HWC were highest in forest lands followed by the range and agricultural lands. Among the SOM fractions, S + SA showed the highest values (5.75, 5.77 and 20.6 g kg^?1 for agriculture, range and forest lands respectively) followed by POM, Si + C, rSOM, and DOC. The concentrations of C and N in the labile fractions obtained the higher values than in the stabilized fractions. Forest lands had the highest amounts of organic C and N among all fractions whereas agricultural lands showed highest values for inorganic C content of soils in different fractions.     

Impacts of organic residue management on the soil C dynamics in a tropical eucalypt plantation on a nutrient-poor sandy soil after three rotations

Harvest residue management is a key issue for the sustainability of short rotation plantations of fast growing tree species established on poor soils and for potential carbon (C) accretion in many soils. By measuring the C isotope composition (δ¹³C) of different soil organic matter fractions and microbial respiration, we examined the effects of organic residue management at harvest on soil C dynamics in a tropical eucalypt plantation established on a savannah at the end of the third rotation on three treatments repeated at each harvest. We compared plots where the standard harvesting method in Congolese commercial plantations was applied (SWH; only removing the debarked commercial-sized boles) with plots where all the aboveground biomass and the litter layer from the previous rotations were removed at harvest (R) and plots where the residues from a whole tree harvest treatment were added (double slash, DS). Organic residue removal decreased the accretion of eucalypt-derived C in coarse and fine particulate organic matter (POM) fractions and in the organo-mineral fraction, resulting in 44% less total soil C in the top soil (0–0.05 m) but did not affect the amount of savannah-derived C in any SOM fraction. In contrast, increasing the amount of harvest residue by 36% in comparison with the reference practice did not increase the amount of C stored in the soil nor the accretion of eucalypt-derived C in any soil organic matter fractions, but the amount of savannah-derived C remaining in the coarse POM fraction was higher. We concluded that carbon accretion may be limited by the low C saturation level of these sandy-structured soils but that higher rates of residue retention may reduce priming on older savannah-derived C.     

The dynamics of organic matter in rock fragments in soil investigated by 14C dating and measurements of 13C

Rock fragments in soil can contain significant amounts of organic carbon. We investigated the nature and dynamics of organic matter in rock fragments in the upper horizons of a forest soil derived from sandstone and compared them with the fine earth fraction (<2 mm). The organic C content and its distribution among humic, humin and non‐humic fractions, as well as the isotopic signatures (Δ¹⁴C and δ¹³C) of organic carbon and of CO₂ produced during incubation of samples, all show that altered rock fragments contain a dynamic component of the carbon cycle. Rock fragments, especially the highly altered ones, contributed 4.5% to the total organic C content in the soil. The bulk organic matter in both fine earth and highly altered rock fragments in the A1 horizon contained significant amounts of recent C (bomb ¹⁴C), indicating that most of this C is cycled quickly in both fractions. In the A horizons, the mean residence times of humic substances from highly altered rock fragments were shorter than those of the humic substances isolated in the fine earth. Values of Δ¹⁴C of the CO₂ produced during basal respiration confirmed the heterogeneity, complexity and dynamic nature of the organic matter of these rock fragments. The weak ¹⁴C signatures of humic substances from the slightly altered rock fragments confirmed the importance of weathering in establishing and improving the interactions between rock fragments and surrounding soil. The progressive enrichment in ¹³C from components with high‐¹⁴C (more recent) to low‐¹⁴C (older) indicated that biological activity occurred in both the fine and the coarse fractions. Hence the microflora utilizes energy sources contained in all the soil compartments, and rock fragments are chemically and biologically active in soil, where they form a continuum with the fine earth.     

The relationship between copper accumulated in vineyard calcareous soils and soil organic matter and iron

The intensive use for over 100 years of copper sulphate (Bordeaux mixture) to fight mildew in vineyards has led to a substantial accumulation of copper (Cu) in surface soils. To assess the effects of such large concentrations, the surface soils of 10 Burgundy vineyards were sampled and analysed for total organic matter (carbon and nitrogen) and metal (copper and iron) contents. Physical (i.e. size fractionation) and chemical (sequential extraction) methods were used to determine the distribution of these elements. The most Cu‐contaminated plots showed the largest accumulation of organic carbon and Cu in the coarse sand and fine sand fractions. Copper was strongly correlated with organic carbon and organic nitrogen in the coarse sand fraction and with organic nitrogen in the fine sand fraction. Copper was also highly correlated with both Fe and organic nitrogen in the clay fraction but not significantly with organic carbon. The sequential extraction showed that Cu was bound mainly to the Fe oxides. However, in the most Cu‐contaminated plots, a part of added Cu was bound to organic matter. This study suggests that Cu protected indirectly the organic matter present in the coarse fractions against biodegradation, and therefore modified the distribution of organic carbon among the particle‐size fractions. Iron appeared as the main factor responsible for Cu accumulation in the clay fraction, mainly through inclusion of Cu in Fe oxyhydroxides and possibly in clay–humus complexes.     

Variation of intra‐aggregate organic carbon affects aggregate formation and stability during organic manure fertilization in a fluvo‐aquic soil

The aggregate formation and stability are controlled by the dynamics of soil organic matters (SOM), but how it is related to SOM chemical composition within different‐sized aggregates is largely unknown during manure fertilization. In this study, the variations of intra‐aggregate organic carbon (OC), including intra‐particulate organic matter (iPOM) and mineral‐associated organic matter, were quantitatively and qualitatively analysed, and then, their effects on aggregate formation and stability were assessed under four treatments: control (CK), mineral fertilizer (NPK), reduced manure (30%M) and manure fertilizers (M). Manure application (M) significantly increased macroaggregate proportion, mean weight diameter (MWD), and OC contents within different‐sized aggregates compared to CK, NPK, and 30%M. The OC accumulation of macroaggregate in M was attributed to OC content increase in silt plus clay subfraction rather than iPOM with more labile organic groups; oppositely, in microaggregate it was located in the relatively stable fine iPOM. The macroaggregate formation and stability were controlled by the fine iPOM within macroaggregates, whose abundant polysaccharide‐C and aliphatic‐C after manure fertilization advanced the microbial growth except for Gram‐positive bacteria, which further promoted macroaggregate formation and stability. The free silt plus clay fraction also affected macroaggregate formation and stability, and its polysaccharide‐C derived from microorganisms or decomposing SOM was positively associated with MWD and macroaggregate proportion. Because polysaccharide‐C can be easily associated with mineral particles, further improving micro‐ or macroaggregation. We conclude that continuous manure fertilization could increase labile SOM accumulation within aggregates and then facilitate microbial growth, which collectively are responsible for aggregate formation and stabilization.