基于激光衍射的土壤粒径测定法的评价与校正

为比较与评价激光法与吸管法测定土壤粒径分布的准确性,该文采用激光法与吸管法测定了23组来自中国13个不同省份或自治区土壤样本的粒径分布,将激光法与传统吸管法的测定结果进行比较,并在此基础上对激光法测定参数进行了修正。结果表明:1)与吸管法相比,激光衍射法低估土壤样品中的黏粒含量,其相对误差为36.33%;高估粉粒含量,其相对误差为36.51%;2)对吸管法与激光衍射法的实测结果进行线性关系分析表明,其中黏粒与粉粒的线性关系较好,决定系数分别为0.91,0.90;3)经过模型转换后,基于激光衍射法的土壤粒径分布结果的相对误差明显降低:黏、粉的相对误差分别降低至16.25%、12.83%,说明激光衍射法可以用于大规模不同类型的土壤粒径分析。该研究可为土壤系统化和规范化的对比研究以及建立基于激光衍射技术的土壤质地划分标准提供依据。     

Influence of fertilization and organic amendments on organic‐carbon fractions in Heilu soil on the loess plateau of China

The influence of fertilization on organic‐carbon fractions separated by density and particle size in Heilu soil (Calcic Kastanozems, FAO) was investigated in a 20‐year (1979–1999) long‐term experiment on the Loess Plateau of China. Compared to an unfertilized treatment, N application alone did not increase total organic carbon (TOC) and its fractions of density and particle size. However, the treatment of N + P fertilization significantly increased salty‐solution–soluble organic carbon (SSOC), microbial biomass C (MB‐C), and organic C associated with fine silt. When manure was applied alone and in combination with N and P fertilizer, the light fraction of organic C (LFOC), SSOC, and MB‐C were increased significantly, and the TOC was as high as that of a native Heilu soil. Organic C associated with different particle‐size fractions was also increased significantly, and the allocation of C among the fractions was altered: the proportions of C in sand (>50 μm), coarse‐silt (20–50 μm), and fine‐clay (<0.2 μm) fractions were increased whereas fine‐silt (2–20 μm) and coarse‐clay (0.2–2 μm) fractions were decreased. It is concluded that N fertilizer alone is not capable of restoring organic‐matter content in the Heilu soils of the Loess Plateau and that C‐containing material like manure and straw is necessary to produce significant increase in soil organic carbon in these soils.     

A routine method to study soil organic matter by particle‐size fractionation: Examples for tropical soils

Abstract

Particle size fractionation is becoming commonly used for studying soil organic matter (OM). However, isolation of clay and silt represents a long and thus tedious step in the fractionation procedure. We propose an approach identical to the one utilized in particle size analysis with an estimation of the recoveries from aliquots ("aliquot”; method) of the 0–2 and 0–20 μm fractions and no entire isolation ("decanting”; method) of clay and silt. In comparison with the “decanting”; method, the fraction and carbon (C) recoveries obtained by the “aliquot”; method were satisfactory, but those of nitrogen (N) being hardly interpretable because of an insufficient accuracy of the determination method. The recommended method saves time and laboratory space and could be used as a routine particle size fractionation of soil OM. Finally, this paper lists various methodological aspects of considerable significance but rarely reported in published studies.     

化肥对黑土不同粒级碳水化合物的影响

本文采集公主岭市长期定位监测基地不施肥和施用不同化肥的黑土,通过超声波分散-离心分离得到细黏粒(<0.2μm)、粗黏粒(0.2～2μm)、粉粒(2～53μm)、细砂粒(53～250μm)、粗砂粒(250～2000μm)5个颗粒级别,分析全土及不同粒级中土壤碳水化合物并进行含量与分布的比较。结果表明,黑土中不同粒级碳水化合物库的性质差异显著,碳水化合物多集中在粉+黏粒中;长期施用化肥后,黑土全土及各粒级碳水化合物库大小和浓度基本上没有变化;粗砂粒级(Gal+Man)(:Ara+Xyl)下降,表明该粒级中植物来源碳水化合物所占比重有所增加,暗示出粗砂粒级对施肥措施更为敏感。     

长期施肥下红壤有机碳及其颗粒组分对不同施肥模式的响应

采集不同施肥24年的红壤,采用物理分组的方法,观测了长期不同施肥下红壤有机碳及其组分变化,并结合历史资料分析了不同施肥模式对红壤有机碳及其颗粒组分的影响。结果表明,化肥配施有机肥（NPKM）处理下红壤总有机碳含量（10.33 g/kg）,砂粒（2000～53 m）、细粉粒（5～2 m）和粘粒（2 m）组分中的有机碳含量显著高于其他处理。与不施肥（CK）相比,施用化肥（NPK、2NPK）和有机肥（NPKM、M）显著地提高了红壤有机碳在砂粒和粘粒中的分配比例,而降低了其在粗粉粒和细粉粒的分配比例。施化肥（NPK、2NPK）、单施有机肥（M）、化肥配施有机肥（NPKM）处理,土壤有机碳的平均固定速率分别为0.05 t/(hm2?a)、0.18 t/(hm2?a)、0.26 t/(hm2?a)。相关分析表明,不同施肥模式下红壤有机碳的固定量与碳投入量之间存在着极显著的线性相关关系（R2=0.909, P0.01）,土壤的固碳效率为8.1%;随着碳投入的增加,粗粉粒和细粉粒有机碳储量逐渐下降,而砂粒和粘粒中碳储量逐渐增加,并且粘粒增加速率要远远高于砂粒。以上结果说明,红壤中有机碳还没有达到饱和,还具有一定的固碳潜力,增加的有机碳主要固持在粘粒中,粘粒是红壤有机碳的主要固持组分。     

Decomposability of organic matter in particle size fractions from field soils with straw incorporation

Soils from two field experiments on straw disposal were fractionated according to particle size using ultrasonic dispersion and gravity-sedimentation in water. Samples of whole soils, clay. silt and sand-size fractions were held for 49 days at 20°C and the CO₂ evolution measured on 14 dates by gas chromatography.Recovery of soil solids. C and N was 99, 98 and 93%, respectively. Most of the soil C and N was in the clay (<2μm). (loamy sand, 50% C and 56% N; sandy loam. 65% C and 68% N), the silt (2–20 μm) having smaller proportions (loamy sand, 41% C and 38% N; sandy loam. 29% C and 27% N). The sand fraction (20–6000 μm) accounted for 4–7% of the organic matter, and 1–2% of the C was water soluble. Straw incorporation generally increased the C and N content of whole soils and size fractions.The decomposition rate constants were higher for the sandy loam than for the loamy sand soil. For both soils, the decomposability of the organic matter decreased in the order: sand > clay ⩾ whole soil > silt. Straw incorporation increased the decomposition rate of whole soil and sand organic matter. whereas the effect of straw on clay and silt respiration was small.Between 58 and 73% of the respiration was from clay, 21–25% from silt and 6–19% from the sand size fraction.     

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.     

长期不同施肥对土壤各粒级组分中氮含量及分配比例的影响

土壤培肥过程中氮素的积累和在各级土壤颗粒中的分配对了解土壤氮素积累机制和氮素的可持续管理具有重要意义。本研究以红壤旱地长期定位试验为基础,采用离心法分离土壤颗粒,通过分析氮素在土壤不同颗粒中的含量,研究长期施肥对土壤中不同粒级土壤氮的分配的影响。结果表明,施肥二十年后,在020 cm土层,施肥处理的全氮含量在1.19~1.98 g/kg 之间,施肥处理全氮含量显著高于不施肥处理（CK）。在2040 cm土层,土壤全氮含量分布在0.59~0.84 g/kg之间,显著低于表层土壤氮含量; 在020 cm土层,与氮磷钾化肥配施处理（NPK）相比,单施或者配施有机肥的土壤与砂粒、 粗粉粒、 细粉粒、 粘粒结合的氮含量分别提高220%、 84%、 46%和26%。而在2040 cm土层,与NPK处理相比,有机肥的施用仅提高了与细粉粒、 粘粒结合的氮含量,降低了与粗粉粒结合的氮含量; 在020 cm土层中,红壤氮素主要分布在粘粒中。2040 cm土层CK、 NPK和氮磷钾配施加秸秆还田处理（NPKS）表现为与粗粉粒结合的氮的分配比例最高,而施用有机肥的处理氮素分布仍以粘粒占比例最高。相关分析表明,土壤表层＜5 m粒级的土壤颗粒中氮含量和作物的经济产量呈显著性正相关。长期施用有机肥可以显著提高表层土壤全氮及与各个颗粒结合氮的含量,不同处理的氮主要保存在粘粒中。而亚表层土壤中,施化肥或者秸秆还田加速了粘粒结合态氮的耗竭,配施有机肥促进了氮在粘粒中的积累,也更有利于土壤全氮的积累,是可持续的氮素管理措施。     

Soil restorative effects of mulching on aggregation and carbon sequestration in a Miamian soil in central Ohio

Soils play a key role in the global carbon cycle, and can be a source or a sink of atmospheric carbon (C). Thus, the effect of land use and management on soil C dynamics needs to be quantified. This study was conducted to assess: (1) the role of aggregation in enhancing soil organic carbon (SOC) and total soil nitrogen (TSN) concentrations for different mulch rates, (2) the association of SOC and TSN with different particle size fractions, and (3) the temporal changes in the SOC concentration within aggregate and particle size fractions with duration of mulching. Two experiments were initiated, one each in 1989 and 1996, on a Crosby silt loam (Aeric Ochraqualf or Stagnic Luvisol) in central Ohio. Mulch treatments were 0, 8, and 16 Mg ha⁻¹ yr⁻¹ without crop cultivation. Soil samples from 0–5 cm and 5–10 cm depths were obtained in November 2000; 4 and 11 years after initiating the experiments. Mulch rate significantly increased SOC and TSN concentrations in the 0–5 cm soil layer only. The variation in the SOC concentration attributed to the mulch rate was 41 per cent after 4 years of mulching and 52 per cent after 11 years of mulching. There were also differences in SOC and TSN concentrations among large aggregate size fractions, up to 2 mm size after 4 years and up to 0ċ5 mm after 11 years of mulching. There were also differences in SOC and TSN concentrations among particle size fractions. Variation in the SOC concentration in relation to particle size was attributed to clay by 45–51 per cent, silt by 34–36 per cent, and to sand fraction by 15–19 per cent. Bulk of the TSN (62–67 per cent) was associated with clay fraction and the rest was equally distributed between silt and sand fractions. The enrichment of SOC and TSN concentrations in the clay fraction increased with depth. The C:N ratio was not affected by the mulch rate, but differed significantly among particle size fractions; being in the order of sand >silt >clay. Copyright © 2003 John Wiley & Sons, Ltd.     

Land-use effects on the composition of organic matter in particle-size separates of soil: I. Lignin and carbohydrate signature

Soil from Eutrochrept A horizons under long-term spruce forest (Sf), mixed deciduous forest (Df), permanent grassland (Gp) and arable rotation (Ar) was fractionated according to particle size and analysed for contents of C, N, lignin-derived phenols and carbohydrates. Whole soil from Sf, Df, Gp and Ar contained 84, 59, 73 and 25 g C kg^?1 soil, respectively. For all sites, the C content declined and C/N ratio increased in the order: clay (<2 μm), silt (2–20 μm), sand (20–2000 μm). Clay and silt were significantly lower in C in Ar than in Sf, Df and Gp, C associated with sand being substantially lower under arable rotation. The yield of lignin-derived phenols decreased and carboxyl functionality and methoxyl demethylation of lignin derivatives increased with decreasing particle size, indicating a progressive lignin alteration. Whole soil from Sf and Gp was substantially higher in vanillyl (V), syringyl (S) and cinnamyl (C) units (VSC) than soil from Df and Ar. Compared to whole soil, clay was depleted and sand enriched in VSC. Only sand appeared to be affected significantly by land use. Sand from Ar and Df was more enriched in VSC than sand from Gp and Sf. Whole soil carbohydrates decreased in the order: Gp>Ar>Df>Sf. Sand- and clay-sized separates were enriched in carbohydrates compared to silt. Carbohydrates in sand were mainly of plant origin whereas microbially-derived sugars accounted for a larger proportion in the clay. Compared to Sf, Df and Gp, clay from Ar was enriched and sand depleted in microbial sugars. Lignin and carbohydrate distribution patterns indicate that organic matter was in a more advanced stage of decomposition in the sand separates from forest than from agricultural A horizons. The forest soils also show a higher degree of oxidative changes in lignin associated with clay. In contrast, differences between silt from the four A horizons were small.     

Losses of carbon and nitrogen with prolonged arable cropping from sandy soils of the South African Highveld

A knowledge of the kinetics of organic matter transformations in arable soils is important for managing them sustainably. Our aim in this study was to elucidate the effects of cropping period on pools of C and N in coarse‐textured savanna soils of the South African Highveld. Composite samples were taken from the top 20 cm of soils (Plinthustalfs) that have been cropped for lengths of time varying from 0 to 98 years in each of three different agro‐ecosystems in the Free State Province of South Africa. Thereafter, soil organic C and N concentrations were determined in the bulk soil (< 2 mm) as well as in the clay (< 2 μm), silt (2–20 μm), fine sand (20–250 μm), and coarse sand (250–2000 μm) separates. Long‐term cultivation of native grassland reduced soil C and N concentrations by 65 and 55%, respectively. Losses of soil organic matter occurred from all particle‐size separates, although rate loss constants increased as particle size increased. The concentrations of organic C reached equilibrium after 34 years for the bulk soil and after 55 years for clay‐size separates. Nevertheless, organic matter attached to silt continued to be lost as the cropping continued, probably due to wind erosion. Changes in soil properties thereby continued even after almost 100 years of cultivation.     

激光粒度仪与吸管法测定土壤机械组成的比较研究——以不同退化程度栗钙土为例

激光粒度仪法作为测量土壤机械组成的新型方法,具有操作简单、速度快的优势,但其适用性与可靠性尚未达成广泛共识。为探究激光粒度仪测定土壤机械组成的准确性与适用性,采集7种退化程度共21份栗钙土土样,使用激光粒度仪与吸管法测定土样机械组成并对比分析。结果显示:激光法测定结果黏粒偏小,而砂粒、粉粒偏大,且随粒径减小误差增大。将两种测定结果进行回归分析,发现砂粒与粉粒转换模型拟合效果理想,黏粒拟合效果差。建立质地三角图发现两种方法得到的质地差异较大,采用转换后数据分析质地,发现质地接近、正确率高,转换效果好。通过扫描电镜对土粒形态观察,发现标准流程不同分散方法下土粒形状与数量均有差异,推测分散方法会影响土壤机械组成的测定结果。激光粒度仪的适用性据测定对象的不同而有差异,对黏粒精度要求高的情况下不宜使用该法,而其他情况下需要对测定结果进行数据转换。     

伊犁河谷不同土地利用方式下土壤粒度特征

为更有效地指导伊犁河谷水土环境的可持续发展,对河谷地区不同土地利用方式下的土壤进行采样,共获得14个剖面98个土壤样品。利用EASY SIZER20测定样品粒度,依据福克—沃德公式计算中值、平均粒径、标准偏差、峰度、偏度,采用Excel,SPSS 19.0等统计软件进行作图和统计分析。结果表明:(1)不同土地利用方式下土壤粒级百分含量虽有不同,但都是以粉粒(2~50μm)、砂粒(50~2 000μm)为主。其中耕地的粉粒、砂粒百分含量均高于荒地,林地、草地的黏粒(2μm)百分含量相当。(2)不同土地利用方式下土壤粒级的变异系数表现出显著性差异。耕地中粉粒、砂粒含量的变异系数普遍大于荒地,黏粒含量的变异系数则相反。(3)不同土地利用方式下土壤粒度特征不同,耕地的平均粒径明显大于草地、荒地、林地,荒地的分选性明显优于耕地、园地。     

有机肥对棕壤不同粒级有机碳和氮的影响

采集棕壤长期肥料定位试验站不施肥和施用不同用量有机肥的土壤,通过超声波分散—离心分离得到细黏粒(<0.2μm)、粗黏粒(0.2～2μm)、粉粒(2～53μm)、细砂粒(53～250μm)和粗砂粒(250～2000μm)5个颗粒级别后,分析全土及不同粒级中土壤有机碳和氮并进行含量与分布的比较。结果表明,有机质主要分布于黏粒级中,其含量占全土有机碳的42.8%、全氮的58.3%,碳氮比随着粒级的增加而逐渐增大,表明氮易于在小粒级中富集。长期施用有机肥后,全土及各粒级有机碳和氮含量均有显著增加;砂粒级中有机碳和氮的富集系数升高,黏粒级中富集系数降低,粉粒级和砂粒级中的碳氮比降低。增加有机肥的用量加强了全土和各粒级对有机碳和氮的积累,同时加强了粉粒级和砂粒级碳氮比降低的程度。     

THE DISTRIBUTION OF LABELLED SUGARS IN SOIL PARTICLE SIZE FRACTIONS AS A MEANS OF DISTINGUISHING PLANT AND MICROBIAL CARBOHYDRATE RESIDUES

Soils of the Countesswells and Insch series incubated with ¹⁴C labelled glucose or plant materials have been separated into clay (< 2 μm), silt, (2–20 μm), fine sand (20–250 μm) and coarse sand (>250μm) fractions and the distribution of individual labelled and unlabelled sugars was determined in each fraction. Both soils contained about 10–15 per cent clay, 18–23 per cent silt and about 60 per cent fine and coarse sand. For all soil samples the concentrations of sugars were usually greatest in the clay, slightly less in the silt, with values in the sand fractions being five or ten times lower, except when fresh plant material was present. In ¹⁴C glucose amended Insch soil, 55 per cent of the radioactivity in sugars (predominantly hexoses) occurred in the clay, 36 per cent in the silt, 3 per cent in the fine sand and 6 per cent in the coarse sand after 28 days incubation. For the Countesswells soil the values were 55, 42, 2 and 1 per cent respectively. In ¹⁴C ryegrass amended soil before incubation. 77 per cent of the radioactivity in sugars (predominantly glucose, arabinose and xylose) was in the coarse sand. After one year's incubation this had fallen to 59 per cent. In soil amended with ¹⁴C cereal rye straw the distribution of radioactivity in sugars after four years incubation was: clay, 21 per cent; silt, 43 per cent; fine sand, 21 per cent; coarse sand, 4 per cent. These distributions were compared with that of the naturally occurring sugars: clay, 31–42 per cent; silt, 40–43 per cent; fine sand, 3–11 per cent; coarse sand, 12–20 per cent.     

Determination of organic carbon and nitrogen in particulate organic matter and particle size fractions of Brookston clay loam soil using infrared spectroscopy

The objective of this study was to determine whether models developed from infrared spectroscopy could be used to estimate organic carbon (C) content, total nitrogen (N) content and the C:N ratio in the particulate organic matter (POM) and particle size fraction samples of Brookston clay loam. The POM model was developed with 165 samples, and the particle size fraction models were developed using 221 samples. Soil organic C and total N contents in the POM and particle size fractions (sand, 2000–53 µm; silt, 53–2 µm; clay, <2 µm) were determined by using dry combustion techniques. The bulk soil samples were scanned from 4000 to 400 cm^?1 for mid‐infrared (MIR) spectra and from 8000 to 4000 cm^?1 for near‐infrared (NIR) spectra. Partial least squares regression (PLSR) analysis and the ‘leave‐one‐out' cross‐validation procedure were used for the model calibration and validation. Organic C and N content and C:N ratio in the POM were well predicted with both MIR‐ and NIR‐PLSR models ( = 0.84–0.92; = 0.78–0.87). The predictions of organic C content in soil particle size fractions were also very good for the model calibration ( = 0.84–0.94 for MIR and = 0.86–0.92 for NIR) and model validation ( = 0.79–0.94 for MIR and = 0.84–0.91 for NIR). The prediction of MIR‐ and NIR‐PLSR models for the N content and the C:N ratio in the sand and clay fractions was also satisfactory ( = 0.73–0.88; = 0.67–0.85). However, the predictions for the N content and C:N ratio in the silt fraction were poor ( = 0.23–0.55; = 0.20–0.40). The results indicate that both MIR and NIR methods can be used as alternative methods for estimating organic C and total N in the POM and particle size fractions of soil samples. However, the NIR model is better for estimating organic C and N in POM and sand fractions than the MIR model, whereas the MIR model is superior to the NIR model for estimating organic C in silt and clay fractions and N in clay fractions.     

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.     

Disruption of soil aggregates by varied amounts of ultrasonic energy in fractionation of organic matter of a clay Latosol: carbon,nitrogen and δ13C distribution in particle‐size fractions

Ultrasonic energy has been widely used to disrupt soil aggregates before fractionating soil physically when studying soil organic matter (SOM). Nevertheless, there is no consensus about the optimum energy desirable to disrupt the soil. We therefore aimed (i) to quantify the effect of varied ultrasonic energies on the recovery of each particle‐size fraction and their C, N and δ¹³C distribution, and (ii) to determine an ideal energy to fractionate SOM of a specific soil. Our results show that the 2000–100 μm particle‐size fraction was composed mainly of unstable aggregates and the 100–2 μm fraction of stable aggregates. Energies of 260–275 J ml^?1 were sufficient to disrupt most of the unstable aggregates and leave stable aggregates. The use of this threshold energy combined with particle‐size fractionation was not satisfactory for all purposes, since litter‐like material and relatively recalcitrant organic carbon present in stable aggregates > 100 μm were recovered in the same pool. An ultrasonic energy of 825 J ml^?1 was not sufficient to stabilize the redistribution of soil mass and organic matter among particle‐size fractions, but at energies exceeding 260–275 J ml^?1 relatively stable aggregates would fall apart and cause a mixture of carbon with varied nature in the clay fraction.     

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.     

The Impact of Agriculture on Soil Texture Due to Wind Erosion

Wind erosion produces textural changes on topsoil of semiarid and arid environments; however, the selection of particles on different textured soils is unclear. Our objectives were to evaluate textural changes induced by wind erosion on cultivated soils of different granulometry and to asses if textural changes produced by wind erosion are linked to aggregation of granulometric particles into different sizes of aggregates formed in contrasting textured soils. Considering this, we studied the particle size distribution (PSD) with full dispersion (PSD_F) of 14 cultivated (CULT) and uncultivated (UNCULT) paired soils and, on selected sites, the PSD with minimum dispersion (PSD_MIN) and the quotient PSD_MIN/F. Results showed that the content of silt plus clay was lower in CULT than in UNCULT in most of the sites. The highest removal of silt was produced in soils with low sand and high silt content; meanwhile, the highest removal of clay was observed in soils with medium sand content. According to PSD_MIN, particles of 250–2,000 μm predominated in the sandy soil, in the loamy soil particles between 50 and 250 μm and in the silty loam soil particles between 2 and 50 μm. For clay sized particles, PSD_MIN/F was lower than 1 in all soils and managements, but this quotient was higher in CULT compared with UNCULT only in the loamy soil. This means a decrease of clay accumulation in aggregates of larger sizes produced by agriculture, which indicates an increase in the risk of removal of these particles by wind in loamy soils. Copyright © 2014 John Wiley & Sons, Ltd.