Using soil organic matter fractions as indicators of soil physical quality

The objective of this study was to evaluate the use of chemical and physical fractions of soil organic matter (SOM ), rather than SOM per se , as indicators of soil physical quality (SPQ ) based on their effect on aggregate stability (AS ). Chemically extracted humic and fulvic acids (HA and FA ) were used as chemical fractions, and heavy and light fractions (HF and LF ) obtained by density separation as physical fractions. The analyses were conducted on medium‐textured soils from tropical and temperate regions under cropland and pasture. Results show that soil organic carbon (SOC ), SOM fractions and AS appear to be affected by land use regardless of the origin of the soils. A general separation of structurally stable and unstable soils between samples of large and small SOC content, respectively, was observed. SOM fractions did not show a better relationship with AS than SOC per se . In both geographical regions, soils under cropland showed the smallest content of SOC , HA and carbon concentration in LF and HF , and the largest HF /LF ratio (proportion of the HF and LF in percent by mass of bulk soil). With significant associations between AS and SOC content (0.79**), FA /SOC (r  = −0.83*^*), HA /FA (r  = 0.58*^*), carbon concentration of LF (r  = 0.69*^*) and HF (r  = 0.70*^*) and HF /LF ratio (r  = 0.80*^*), cropland showed lowest AS . These associations indicate that SOM fractions provide information about differences in SOM quality in relation to AS and SPQ of soils from tropical and temperate regions under cropland and pasture.     

Factors controlling mineralization of soil organic matter in the Eurasian steppe

To understand the dynamics of soil organic matter (SOM) in the Eurasian steppe, several soil and meteorological properties were tested in order to estimate the amounts of potentially mineralizable organic carbon (PMC) and nitrogen (PMN). Total 41 surface soil samples were collected in Ukraine and Kazakhstan from cropland, forest, grassland, and desert ecosystems. The fresh soils were incubated for 133 days under constant temperature and moisture conditions, and the CO₂ emissions and the mineral N from the soils were monitored. PMC and PMN were determined by fitting models to the cumulative curves of the CO₂ and the mineral N. Tested soil properties included soil pH, sand, silt and clay contents, carbon and nitrogen contents of light fraction (LF, <1.6 g cm^?3) and heavy fraction (HF), and C/N ratio of LF and HF. The meteorological properties considered were mean annual temperature and precipitation. Using multiple regression analysis with the stepwise method, PMC was well estimated by carbon content of LF (LFC) and clay content, compared to the simple correlation with organic carbon (OC). Similarly, PMN was better determined by nitrogen content of LF (LFN) and clay content. These results suggest the partially labile nature of clay-associating OM and of LFC and LFN. The higher PMC and PMN in the forest and grassland sites would be attributed to the higher LFC and LFN, while the lower LFC and LFN in cropland sites would suggest the relatively higher contribution of clay-associating OM to PMC and PMN.     

Soil organic matter dynamics along a rice chronosequence in north-eastern Argentina: Evidence from natural C abundance and particle size fractionation

We studied the consequences of rice cultivation and its subsequent abandonment for soil organic matter (SOM) dynamics in north-eastern Argentina. Two chronosequences, which included a pristine grassland with C4 vegetation as a control, and several stages of rice (C3) fields abandoned for 1, 2, 4, 6 and 15 years were selected, and soil samples from the first 10 cm were gathered from each plot. Natural ¹³C abundance coupled with particle-size fractionation were employed to characterize SOM changes through time discriminated by SOM origin. Soil samples up to 50 cm were also collected throughout one chronosequence. Most changes in SOM occurred on the first 20 cm layer and, bulk density, carbon and nitrogen content, as well as δ¹³C remained similar at greater depths. After the rice cropping, the bulk density was slightly greater than in the natural grassland, and remained stable after the abandonment. Carbon and nitrogen contents remained almost stable in the surface layer during the cultivation. δ¹³C varied accordingly with the changes in vegetation cover with a C4 signature in the natural grassland and mainly a C3 signature in the rice fields. The abandonment of the rice cropping induced a decrease of the soil organic matter content, mainly of natural grassland origin, during the first 4 years. When the abandonment extended, the SOM content (from C4 origin) increased slowly and after 15 years, was almost the same as that of the natural grassland. The carbon turnover was greater in the coarser fractions than in the finer ones, confirming that soil organic carbon in the sand fraction was relatively labile. However, all the fractions were affected by inputs and outputs of C derived from rice and natural grassland. This fact could indicate that the former protected carbon could become less stable due to cultivation.     

Soil organic carbon stocks,distribution, and composition affected by historic land use changes on adjacent sites

Historic alterations in land use from forest to grassland and cropland to forest were used to determine impacts on carbon (C) stocks and distribution and soil organic matter (SOM) characteristics on adjacent Cambisols in Eastern Germany. We investigated a continuous Norway spruce forest (F-F), a former cropland afforested in 1930 (C-F), and a grassland deforested in 1953 (F-G). For C and N stocks, we sampled the A and B horizons of nine soil pits per site. Additionally, we separated SOM fractions of A and B horizons by physical means from one central soil pit per pedon. To unravel differences of SOM composition, we analyzed SOM fractions by ¹³C-CPMAS NMR spectroscopy and radiocarbon analysis. For the mineral soils, differences in total C stocks between the sites were low (F-F = 8.3 kg m⁻²; C-F = 7.3 kg m⁻²; F-G = 8.2 kg m⁻²). Larger total C stocks (+25%) were found under continuous forest compared with grassland, due to the C stored within the organic horizons. Due to a faster turnover, the contents of free particulate organic matter (POM) were lower under grassland. High alkyl C/O/N-alkyl C ratios of free POM fractions indicated higher decomposition stages under forest (1.16) in relation to former cropland (0.48) and grassland (0.33). Historic management, such as burning of tree residues, was still identifiable in the subsoils by the composition and ¹⁴C activity of occluded POM fractions. The high potential of longer lasting C sequestration within fractions of slower turnover was indicated by the larger amounts of claybound C per square meter found under continuous forest in contrast to grassland.     

Factors affecting the molecular structure and mean residence time of occluded organics in a lithosequence of soils under ponderosa pine

Occluded, or intra-aggregate, soil organic matter (SOM) comprises a significant portion of the total C pool in forest soils and often has very long mean residence times (MRTs). However, occluded C characteristics vary widely among soils and the genesis and composition of the occluded organic matter pool are not well understood. This work sought to define the major controls on the composition and MRT of occluded SOM in western U.S. conifer forest soils with specific focus on the influence of soil mineral assemblage and aggregate stability. We sampled soils from a lithosequence of four parent materials (rhyolite, granite, basalt, and dolostone) under Pinus ponderosa. Three pedons were excavated to the depth of refusal at each site and sampled by genetic horizon. After density separation at 1.8 g cm⁻³ into free/light, occluded and mineral fractions, the chemical nature and mean residence time of organics in each fraction were compared. SOM chemistry was explored through the use of stable isotope analyses, ¹³C NMR, and pyrolysis GC/MS. Soil charcoal content estimates were based on ¹³C NMR analyses. Estimates of SOM MRT were based on steady-state modeling of SOM radiocarbon abundance measurements. Across all soils, the occluded fraction was 0.5–5 times enriched in charcoal in comparison to the bulk soil and had a substantially longer MRT than either the mineral fraction or the free/light fraction. These results suggest that charcoal from periodic burning is the primary source of occluded organics in these soils, and that the structural properties of charcoal promote its aggregation and long-term preservation. Surprisingly, aggregate stability, as measured through ultrasonic dispersion, was not correlated with occluded SOM abundance or MRT, perhaps raising questions of how well laboratory measurements of aggregate stability capture the dynamics of aggregate turnover under field conditions. Examination of the molecular characteristics of the occluded fraction was more conclusive. Occluded fraction composition did not change substantially with soil mineral assemblage, but was increasingly enriched in charcoal with depth relative to bulk SOM. Enrichment levels of ¹³C and ¹⁵N suggested a similar degree of microbial processing for the free/light and occluded fractions, and molecular structure of occluded and free/light fractions were also similar aside from charcoal enrichment in the occluded fraction. Results highlight the importance of both fire and aggregate formation to the long-term preservation of organics in western U.S. conifer forests which experience periodic burning, and suggest that the composition of occluded SOM in these soils is dependent on fire and the selective occlusion of charcoal.     

Soil Na+ concentration controls salt-affected soil organic matter components in Hetao region China

Purpose

There is little knowledge on the organic matter fractions of salt-affected soil aggregates. This study aimed at investigating characteristics of salt-affected soil organic carbon components and the relationships between soil salt concentration and soil organic carbon component content.

Materials and methods

Five typical salt-affected soils in Hetao region China were collected and analyzed for light (LF) and heavy fraction (HF) in different water-stable aggregates. And the soil organic carbon components were measured by Fourier transform infrared (FTIR) and pyrolysis-gas chromatography/mass spectrometer (Py–GC/MS).

Results and discussion

The results showed that the salt-affected soils were dominant in 53–10-μm water-stable aggregates, 61–80% in the bulk soil, and very low in >?250-μm macro-aggregates, less than 7.06% in the bulk soil. The proportions of >?250-μm macro-aggregates and the mean weight diameter (MWD) were negatively correlated to Na⁺ concentration (p?<?0.05). Furthermore, the macro-aggregates were generally higher in total organic carbon (TOC) and accordingly higher C/N ratio than those in micro-aggregates. Heavy fractions (HF) from both >?53 μm and <?53-μm soil aggregates accounted for 99.30–99.83% of the bulk soil and contained 89.6–98.5% lower TOC and accordingly 49.2–84.8% lower C/N ratio than those in light fractions (LF). The LFs were high in lignin (7.27–34.02% in total pyrolysis products, 19.89% on average) and alkane/alkene-derived compounds (9.51–37.21%, 23.18% on average), but low in N-containing compounds (0–3.64%, 1.71% on average), while HFs were high in both alkane/alkene (4.38–27.46%, 15.06% on average) and N-containing compounds (7.45–26.45%, 13.98% on average), but low in lignin-derived compounds (1.13–8.75%, 3.86% on average).

Conclusions

The tested salt-affected soils were predominant in 53–10-μm micro-aggregates, which was caused by the Na⁺ dispersion effect on soil aggregates. Most SOM was stored in HF that contained high N-containing compounds and low C/N ratios. Our results suggested that the components of SOM were mainly controlled by the soil Na⁺ concentration.

     

Towards understanding of carbon stocks and stabilization in volcanic ash soils in natural Andean ecosystems of northern Ecuador

Volcanic ash soils contain very large stocks of soil organic matter (SOM) per unit area. Consequently, they constitute potential sources or sinks for the greenhouse gas carbon dioxide. Whether soils become a net carbon source or sink with climate and/or land‐use change depends on the stability of SOM against decomposition, which is influenced by stabilization mechanisms in the soil. To quantify organic carbon stocks and to clarify the importance of chemical and physical soil characteristics for carbon stabilization in volcanic ash soils, we applied selective extraction techniques, performed X‐ray diffraction analysis of the clay fraction and estimated pore‐size distribution of soils under natural upper montane forest and grassland (páramo) in the Ecuadorian Andes. Our results show that organic carbon stocks under both vegetation types are roughly twice as large as previously reported global averages for volcanic ash soils. SOM stabilization is suggested to be dominantly influenced by the following chemical and physical soil characteristics: (i) direct stabilization of SOM in organo‐metallic (Al‐humus) complexes, explaining at most 40% of carbon accumulation, (ii) indirect protection of SOM (notably aliphatic compounds) through low soil pH and toxic levels of Al, and probably also (iii) physical protection of SOM caused by a very large micro‐porosity. Moreover, in the case of the forest soils, inherent recalcitrance of OM itself was responsible for substantial accumulation in ectorganic horizons. Both vegetation types contributed to soil acidification, thus increasing SOM accumulation.     

Role of Soil Organic Matter in Maintaining Sustainability of Cropping Systems

Soil organic matter (SOM) has long been recognized as an important indicator of soil productivity. The SOM refers to the organic fraction of the soil exclusive of undecayed plant and animal residues. It plays a crucial role in maintaining sustainability of cropping systems by improving soil physical (texture, structure, bulk density, and water-holding capacity), chemical (nutrient availability, cation exchange capacity, reduced aluminum toxicity, and allelopathy), and biological (nitrogen mineralization bacteria, dinitrogen fixation, mycorrhizae fungi, and microbial biomass) properties. The preservation of SOM is crucial to ensure long-term sustainability of agricultural ecosystems. Improvement/preservation of soil organic matter can be achieved by adopting appropriate soil and crop management practices. These practices include conservation tillage, crop rotation, use of organic manures, increasing cropping intensity, use of adequate rate of chemical fertilizers, incorporation of crop residues, liming acidic soils, and keeping land under pasture. Organic matter can adsorb heavy metals in the soils, which reduce toxicity of these metals to plants and reduce their escape to ground water. Similarly, SOM also adsorbs herbicides, which may inhibit contamination of surface and ground water. Furthermore, SOM also functions as a sink to organic carbon and mitigates carbon dioxide (CO₂) gas escape to the environment. Globally, soil organic matter contains about three times as much carbon as found in the world's vegetation. Hence, organic matter plays a critical role in the global carbon balance that is thought to be the major factor affecting global warming. Overall, adequate amounts of soil organic matter maintain soil quality, preserve sustainability of cropping systems, and reduce environmental pollution.     

Impact of tillage and crop rotation on light fraction and intra-aggregate soil organic matter in two Oxisols

It is well known that no-tillage (NT) practices can promote greater stocks of soil organic matter (SOM) in the soil surface layer compared to conventional tillage (CT) by enhancing the physical protection of aggregate-associated C in temperate soils. However, this link between tillage, aggregation and SOM is less well established for tropical soils, such as Oxisols. The objective of this study was to investigate the underlying mechanisms of SOM stabilization in Oxisols as affected by different crop rotations and tillage regimes at two sites in southern Brazil. Soils were sampled from two agricultural experiment sites (Passo Fundo and Londrina) in southern Brazil, with treatments comparing different crop rotations under NT and CT management, and a reference soil under native vegetation (NV). Free light fraction (LF) and intra-aggregate particulate organic matter (iPOM) were isolated from slaking-resistant aggregates. Of the total C associated with aggregates, 79–90% was found in the mineral fraction, but there were no differences between NT and CT. In contrast, tillage drastically decreased LF-C concentrations in the 0–5 cm depth layer at both sites. In the same depth layer of NT systems at Londrina, the concentrations of iPOM-C were greater when a legume cover crop was included in the rotation. At Londrina, the order of total iPOM-C levels was generally NV > NT > CT in the 0–5 cm depth interval, but the difference between NT and CT was much less than in Passo Fundo. At Passo Fundo, the greatest concentrations and differences in concentrations across tillage treatments were found in the fine (53–250 μm) iPOM fractions occluded within microaggregates. In conclusion, even though no aggregate hierarchy exists in these Oxisols, our results corroborate the concept of a stabilization of POM-C within microaggregates in no-tillage systems, especially when green manures are included in the rotation.     

Temporal changes in soil carbon and nitrogen storage in a hybrid poplar chronosequence in northern Alberta

Sequestering C in biomass and soils in hybrid poplar plantations can help mitigate global climate change caused by the rising atmospheric CO₂ concentration. However, the impact of the establishment of hybrid poplar plantations on C and N storage and dynamics is poorly understood. We studied the distribution and temporal changes of C and N in soil organic matter (SOM) density fractions in 2-, 5-, 11-, and 13-year-old (age as in 2006) hybrid poplar stands that form a chronosequence by sampling the plantations in both 2004 and 2006. Sodium polytungstate (SPT, density = 1.6 g mL^- 1) was used to fractionate the soil into light (LF, density < 1.6 g mL^- 1), occluded light (LFo, density < 1.6 g mL^- 1) and heavy fractions (HF density > 1.6 g mL^- 1). The results showed that C and N concentrations (g kg^- 1 of fraction) in the SOM density fractions decreased in the order of LFo > LF > HF, while the C/N ratio was in the order of LF > LFo > HF. The amount of C and N stored in the LF, LFo and HF fractions and bulk soil in the top 10 cm of soil was: 149-504, 70-336, 1380-2876 and 1617-3776 g m^- 2, respectively, for C, and 6-26, 3-20, 149-271 and 152-299 g m^- 2, respectively, for N. From 2004 to 2006, C and N storage decreased in the LF and LFo fractions but increased in the HF fraction in the youngest stand. However, stand-age effects were likely muted by high inherent soil variability among the stands. Carbon storage in the light fraction was responsive in the short term to hybrid poplar plantation establishment.     

Biological, chemical and thermal indices of soil organic matter stability in four grassland soils

The various ecosystem functions of soil organic matter (SOM) depend on both its quantity and stability. Numerous fractionation techniques have been developed to characterize SOM stability, and thermal analysis techniques have shown promising results to describe the complete continuum of SOM in whole soil samples. However, the potential link between SOM thermal stability and biological or chemical stability has not yet been adequately explored. The objective of this study was to compare conventional chemical and biological methods used to characterize SOM stability with results obtained by thermal analysis techniques. Surface soil samples were collected from four North American grassland sites along a continental mean annual temperature gradient, each with a native and cultivated land use. Soil organic C concentrations ranged from 6.8 to 33 g C kg⁻¹ soil. Soils were incubated for 588 days at 35 °C, and C mineralization rates were determined periodically throughout the incubation by measuring CO₂ concentration using an infrared gas analyzer (IRGA) to calculate biological indices of SOM stability. Hot-water extractable organic C (HWEOC) contents were determined before and after incubation as chemical indices. Finally, samples from before and after incubation were analyzed by simultaneous thermal analysis (i.e., thermogravimetry (TG) and differential scanning calorimetry (DSC)) to determine thermal indices of SOM stability. Long-term incubation resulted in the mineralization of up to 33% of initial soil C. The number of days required to respire 5% of initial soil organic carbon (SOC), ranged from 27 to 115 days, and is proposed as a standardized biological index of SOM stability. The number of days was greater for cultivated soils compared to soils under native vegetation, and generally decreased with increasing site mean annual temperature. HWEOC (as % of initial SOC) did not show consistent responses to land use, but was significantly lower after long-term incubation. Energy density (J mg⁻¹ OM) was greater for soils under native vegetation compared to cultivated soils, and long-term incubation also decreased energy density. The temperatures at which half of the mass loss or energy release occurred typically showed larger responses to land use change than to incubation. Strong correlations demonstrated a link between the thermal and biogeochemical stability of SOM, but the interpretation of the thermal behavior of SOM in bulk soil samples remains equivocal because of the role the mineral component and organo-mineral interactions.     

Carbon storage in loess derived surface soils from Central Germany: Influence of mineral phase variables

The influence of the soil mineral phase on organic matter storage was studied in loess derived surface soils of Central Germany. The seven soils were developed to different genetic stages. The carbon content of the bulk soils ranged from 8.7 to 19.7 g kg^—1. Clay mineralogy was confirmed to be constant, with illite contents > 80 %. Both, specific surface area (SSA, BET‐N₂‐method) and cation exchange capacity (CEC) of bulk soils after carbon removal were better predictors of carbon content than clay content or dithionite‐extractable iron. SSA explained 55 % and CEC 54 % of the variation in carbon content. The carbon loadings of the soils were between 0.57 and 1.06 mg C m^—2, and therefore in the ”︁monolayer equivalent” (ME) level. The increase in SSA after carbon removal (ΔSSA) was significantly and positively related to carbon content (r² = 0.77). Together with CEC of carbon‐free samples, ΔSSA explained 90 % of the variation in carbon content. Clay (< 2 μm) and fine silt fractions (2—6.3 μm) contained 68—82 % of the bulk soil organic carbon. A significantly positive relationship between carbon content in the clay fraction and in the bulk soil was observed (r² = 0.95). The carbon pools of the clay and fine silt fractions were characterized by differences in C/N ratio, δ¹³C ratio, and enrichment factors for carbon and nitrogen. Organic matter in clay fractions seems to be more altered by microbes than organic matter in fine silt fractions. The results imply that organic matter accumulates in the fractions of smallest size and highest surface area, apparently intimately associated with the mineral phase. The amount of cations adhering to the mineral surface and the size of a certain and specific part of the surface area (ΔSSA) are the mineral phase properties which affect the content of the organic carbon in loess derived arable surface soils in Central Germany most. There is no monolayer of organic matter on the soil surfaces even if carbon loadings are in the ME level.     

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.     

Response of labile soil organic matter to changes in forest vegetation in subtropical regions

Labile soil organic matter (SOM) can sensitively respond to changes in land use and management practices, and has been suggested as an early and sensitive indicator of SOM. However, knowledge of effects of forest vegetation type on labile SOM is still scarce, particularly in subtropical regions. Soil microbial biomass C and N, water-soluble soil organic C and N, and light SOM fraction in four subtropical forests were studied in subtropical China. Forest vegetation type significantly affected labile SOM. Secondary broadleaved forest (SBF) had the highest soil microbial biomass, basal respiration and water-soluble SOM, and the pure Cunninghamia lanceolata plantation (PC) the lowest. Soil microbial biomass C and N and respiration were on average 100%, 104% and 75%, respectively higher in the SBF than in the PC. The influence of vegetation on water-soluble SOM was generally larger in the 0–10 cm soil layer than in the 10–20 cm. Cold- and hot-water-soluble organic C and N were on average 33–70% higher in the SBF than in the PC. Cold- and hot-soluble soil organic C concentrations in the coniferous-broadleaved mixed plantations were on average 38.1 and 25.0% higher than in the pure coniferous plantation, and cold- and hot-soluble soil total N were 51.4 and 14.1% higher, respectively. Therefore, introducing native broadleaved trees into pure coniferous plantations increased water-soluble SOM. The light SOM fraction (free and occluded) in the 0–10 cm soil layer, which ranged from 11.7 to 29.2 g kg⁻¹ dry weight of soil, was strongly affected by vegetation. The light fraction soil organic C, expressed as percent of total soil organic C, ranged from 18.3% in the mixed plantations of C. lanceolata and Kalopanax septemlobus to 26.3% in the SBF. In addition, there were strong correlations among soil organic C and labile fractions, suggesting that they were in close association and partly represented similar C pools in soils. Our results indicated that hot-water-soluble method could be a suitable measure for labile SOM in subtropical forest soils.     

滇东喀斯特山原红壤退化过程中土壤剖面团聚体和有机质变异

[目的]揭示山原红壤的退化机理及效应,为滇东高原的石漠化效应研究及水土保持工作的开展提供科学依据。[方法]以滇东山原红壤典型发育地带为研究对象,对山原红壤退化过程中灌丛、草地、松林、红裸土剖面的团聚体特征和有机质分布规律进行研究分析。[结果]山原红壤退化过程中干筛法结果显示以大团聚体为主,并随着土层深度的增加而减少;湿筛法结果显示以微团聚体含量最高,灌丛、草地、松林在剖面上整体呈现出与干筛大团聚体一致的规律,红裸土呈现出:0—90cm层(B层)90—100cm层(C层)。土壤的稳定性和有机质含量在退化过程中基本呈现出:灌丛草地松林红裸土;随着土层深度的增加,灌丛、草地、松林土壤团聚体稳定性和物理性质逐渐劣化,有机质含量减少,红裸土则呈现出相反的规律;与A层、B层相比,较深层次的C层团聚体稳定性和有机质含量差异显著降低。[结论]有机质与平均重量直径、几何平均直径、2mm粒级水稳性团聚体含量呈极显著正相关,与分形维数呈极显著负相关,增加有机质的含量应该是恢复和改良红裸土结构的重要手段。     

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.     

Soil organic matter fractions as early indicators for carbon stock changes under different land-use?

With respect to carbon sequestration in soil, attempts have been made to identify soil organic matter (SOM) fractions that respond more rapidly to changes in land-use than bulk SOM, which could thus serve as early indicators for the overall stock change. We used a combination of physical fractionation (size and density separation) and chemical characterisation (C-to-N ratios, CuO lignin signature, ¹³C NMR spectroscopy) to identify sensitive SOM fractions in an agricultural system with sandy dystric cambisols in Bavaria, Germany, 7 years after a land-use change. Land-use types included long-term arable land and grassland, and conversion from one system to the other. Soil carbon and nitrogen contents in 0–3 cm increased from 14 to 39 mg organic carbon g⁻¹ soil, and from 1.7 to 3.9 mg nitrogen g⁻¹ soil in the following order: permanent arable, conversion grassland to arable, conversion arable to grassland, and permanent grassland. Wet sieving and ultrasonic dispersion with 22 J ml⁻¹ released <5% and 60% to 80%, respectively, of the amount of particles >20 μm relative to complete dispersion. The most sensitive fraction, with respect to land-use, was SOM in the fraction >20 μm not released after sequential wet sieving and ultrasonic dispersion. In contrast, the proportion of free light (wet sieving, density <1.8 g cm⁻³) and occluded light (ultrasonic dispersion with 22 J ml⁻¹, <1.8 g cm⁻³) particulate organic matter (POM) showed no clear response to land-use. The structural composition of POM indicated its vegetation origin with a selective enrichment of lignin and a loss of O-alkyl C relative to its plant precursors. Decomposition of the occluded light POM was only slightly advanced relative to the free light POM. In mineral fractions <20 μm, SOM was significantly more transformed than in the coarse fractions, as shown by NMR spectroscopy; however, it revealed no specific land-use pattern. An exception to this was the proportion of O-alkyl C in the clay fraction, which increased with SOC content. Ratios of alkyl to O-alkyl C in mineral fractions <20 μm differentiated samples gave a better differentiation of samples than the C-to-N ratios. We conclude that neither free nor occluded light POM are appropriate early indicators for changes in land-use at the investigated sites; however, total SOM, its distribution with depth, and SOM allocated in stable aggregates >20 μm were more sensitive.     

Properties of soil particle size separates after 40 years of continuous corn

Abstract

Changes in chemical and mineralogical characteristics associated with different particle size fractions in soil after 40 years of continuous production of corn by the conventional tillage method (CC) as compared with those of an adjacent native grassland site (NG) are investigated. Results indicate that corn cropping in a soil previously supporting native vegetation produces a decline in total and humified organic matter, phenolic compounds, enzymatic activities, cation exchange capacity (CEC), and hydrosoluble ions, both in the whole soil and in its particle‐size separates. The’ largest losses in organic carbon (C) and nitrogen (N) contents of the cultivated soil were observed in the sandy fractions, the lowest in the silt+clay separates. The humification index (HI) indicates a higher degree of humification of the organic matter in NG than in CC samples. For both NG and CC sites the finest fraction (silt+clay) resulted to be enriched in organic C, total N, humus, phenolic compounds, enzyme activity, CEC, and hydrosoluble ions with the only exception of mineral N forms and sulphates (SO₄). Slight differences were observed in the mineralogical composition of NG and CC soils. The sandy fractions of NG showed greater amounts of phyllosilicates while a lower content was found in the silt+clay fraction of CC as a consequence of a crumbling of parent rock into small pieces induced by repeated tillage practices.     

The role of mineralization of the organic matter of soddy-podzolic and peat bog soils in the accumulation of <Superscript>137</Superscript>Cs by plants

The role of mineralization of soil organic matter (SOM) in the mobilization of ¹³⁷Cs was estimated on the basis of data on the biokinetic fractionation of the organic matter of soddy-podzolic sandy-loam and peat bog soils and on the coefficients of the soil-to-plant transfer of radiocesium under field conditions. The peat bog soils were richer than the soddy-podzolic soils in the total organic carbon (by 7.9–23.8 times), the potentially mineralizable carbon (by 2.4–6.5 times), and the carbon of the microbial biomass (by 2.9–4.6 times). The agricultural use of the soddy-podzolic and peat bog soils led to a decrease in the SOM mineralization capacity by 1.1–1.8 and 1.4–2.0 times, respectively. Simultaneously, the portions of the easily, moderately, and difficultly mineralizable fraction of the SOM active pool changed. The coefficients of the ¹³⁷Cs transfer from the peat bog soils to plants were 3.3–17.6 times higher than those for the soddy-podzolic soils. The content of ¹³⁷Cs in plants grown on the peat bog soils was 2–65 times higher than that in the mobile (salt-extractable) soil pool by the beginning of the growing season. Strong positive linear correlations were found between the coefficients of the soil-to-plant transfer of ¹³⁷Cs and the total content of the SOM, the content of the microbial biomass, the content of the potentially mineralizable carbon, and the intensity of its mineralization. It was concluded that the decisive factors controlling the intensity of the ¹³⁷Cs transfer from mineral and organic soils into plants are the SOM content and its mineralization potential. The mineralization of the SOM is accompanied by the release of both ¹³⁷Cs and mineral nitrogen; the latter facilitates the transfer of radiocesium into plants.     

Organic matter in density fractions of water-stable aggregates in silty soils: Effect of land use

The location of soil organic matter (SOM) within the soil matrix is considered a major factor determining its turnover, but quantitative information about the effects of land cover and land use on the distribution of SOM at the soil aggregate level is rare. We analyzed the effect of land cover/land use (spruce forest, grassland, wheat and maize) on the distribution of free particulate organic matter (POM) with a density <1.6 g cm⁻³ (free POM_<1.6), occluded particulate organic matter with densities <1.6 g cm⁻³ (occluded POM_<1.6) and 1.6-2.0 g cm⁻³ (occluded POM_1.6-2.0) and mineral-associated SOM (>2.0 g cm⁻³) in size classes of slaking-resistant aggregates (53-250, 250-1000, 1000-2000, >2000 μm) and in the sieve fraction <53 μm from silty soils by applying a combined aggregate size and density fractionation procedure. We also determined the turnover time of soil organic carbon (SOC) fractions at the aggregate level in the soil of the maize site using the ¹³C/¹²C isotope ratio. SOM contents were higher in the grassland soil aggregates than in those of the arable soils mainly because of greater contents of mineral-associated SOM. The contribution of occluded POM to total SOC in the A horizon aggregates was greater in the spruce soil (23-44%) than in the grassland (11%) and arable soils (19%). The mass and carbon content of both the free and occluded POM fractions were greater in the forest soil than in the grassland and arable soils. In all soils, the C/N ratios of soil fractions within each aggregate size class decreased in the following order: free POM_<1.6>occluded POM_<1.6-2.0>mineral-associated SOM. The mean age of SOC associated with the <53 μm mineral fraction of water-stable aggregates in the Ap horizon of the maize site varied between 63 and 69 yr in aggregates >250 μm, 76 yr in the 53-250 μm aggregate class, and 102 yr in the sieve fraction <53 μm. The mean age of SOC in the occluded POM increased with decreasing aggregate size from 20 to 30 yr in aggregates >1000 μm to 66 yr in aggregates <53 μm. Free POM had the most rapid rates of C-turnover, with residence times ranging from 10 yr in the fraction >2000 μm to 42 yr in the fraction 53-250 μm. Results indicated that SOM in slaking-resistant aggregates was not a homogeneous pool, but consisted of size/density fractions exhibiting different composition and stability. The properties of these fractions were influenced by the aggregate size. Land cover/land use were important factors controlling the amount and composition of SOM fractions at the aggregate level.