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1.
Association of organic matter (OM) with minerals is an important pathway in the formation of stable OM in soil. While the importance of mineral–organic associations (MOA) in regulating soil carbon cycling has been rigorously demonstrated by empirical evidence, knowledge about the molecular‐scale arrangement of OM at mineral surfaces is still lacking. Such knowledge is urgently needed to disentangle the mechanisms of long‐term storage of soil OM. Based on indirect observations regarding the formation, composition, and structure of MOA, a conceptual multilayer model was proposed by Kleber et al. in 2007 to foster debate and help elucidating the structure and reactivity of MOA. According to this model, the associated OM at mineral surfaces is discrete and self‐organized into a multilayer structure. In this review, we aim to collect and evaluate existing studies that used this model to explain biogeochemical processes at mineral–organic interfaces, and based on this, assess the applicability of the model. The multilayer model has seen extensive adoption within soil science and related fields. In general, existing studies either support the concept of a patchy distribution of adsorbed OM on mineral surfaces or advocate that OM can be coprecipitated with nanosized poorly crystalline minerals or hydrolysable metals. However, the evidence for the patchy distribution of adsorbed OM cannot support the multilayer model on its own. There is little consensus about the role of N‐rich OM in forming the contact zone according to the multilayer model but surface conditioning by different classes of organic compounds appears to be an essential factor for the overall adsorption of OM. Nevertheless, large uncertainty still remains with respect to multilayer‐like organization of MOA. By taking advantage of recent developments in surface analytical sciences and computational chemistry, a rigid experimental testing of the multilayer model at the molecular level is still required and awaits to be integrated into improved concepts of MOA formation and OM stabilization.  相似文献   

2.
The organic matter (OM) in biopore walls and aggregate coatings may be important for sorption of reactive solutes and water as well as for solute mass exchange between the soil matrix and the preferential flow (PF) domains in structured soil. Structural surfaces are coated by illuvial clay‐organic material and by OM of different origin, e.g., earthworm casts and root residues. The objectives were to verify the effect of OM on wettability and infiltration of intact structural surfaces in clay‐illuvial horizons (Bt) of Luvisols and to investigate the relevance of the mm‐scale distribution of OM composition on the water and solute transfer. Intact aggregate surfaces and biopore walls were prepared from Bt horizons of Luvisols developed from Loess and glacial till. The mm‐scale spatial distribution of OM composition was scanned using diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy. The ratio between alkyl and carboxyl functional groups in OM was used as potential wettability index (PWI) of the OM. The infiltration dynamics of water and ethanol droplets were determined measuring contact angles (CA) and water drop penetration times (WDPT). At intact surfaces of earthworm burrows and coated cracks of the Loess‐Bt, the potential wettability of the OM was significantly reduced compared to the uncoated matrix. These data corresponded to increased WDPT, indicating a mm‐scaled sub‐critical water repellency. The relation was highly linear for earthworm burrows and crack coatings from the Loess‐Bt with WDPT > 2.5 s. Other surfaces of the Loess‐Bt and most surfaces of the till‐derived Bt were not found to be repellent. At these surfaces, no relations between the potential wettability of the OM and the actual wettability of the surface were found. The results suggest that water absorption at intact surface structures, i.e., mass exchange between PF paths and soil matrix, can be locally affected by a mm‐scale OM distribution if OM is of increased content and is enriched in alkyl functional groups. For such surfaces, the relation between potential and actual wettability provides the possibility to evaluate the mm‐scale spatial distribution of wettability and sorption and mass exchange from DRIFT spectroscopic scanning.  相似文献   

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

4.
Based on recent findings in the literature, we developed a process‐oriented conceptual model that integrates all three process groups of organic matter (OM) stabilization in soils namely (1) selective preservation of recalcitrant compounds, (2) spatial inaccessibility to decomposer organisms, and (3) interactions of OM with minerals and metal ions. The model concept relates the diverse stabilization mechanisms to active, intermediate, and passive pools. The formation of the passive pool is regarded as hierarchical structured co‐action of various processes that are active under specific pedogenetic conditions. To evaluate the model, we used data of pool sizes and turnover times of soil OM fractions from horizons of two acid forest and two agricultural soils. Selective preservation of recalcitrant compounds is relevant in the active pool and particularly in soil horizons with high C contents. Biogenic aggregation preserves OM in the intermediate pool and is limited to topsoil horizons. Spatial inaccessibility due to the occlusion of OM in clay microstructures and due to the formation of hydrophobic surfaces stabilizes OM in the passive pool. If present, charcoal contributes to the passive pool mainly in topsoil horizons. The importance of organo‐mineral interactions for OM stabilization in the passive pool is well‐known and increases with soil depth. Hydrophobicity is particularly relevant in acid soils and in soils with considerable inputs of charcoal. We conclude that the stabilization potentials of soils are site‐ and horizon‐specific. Furthermore, management affects key stabilization mechanisms. Tillage increases the importance of organo‐mineral interactions for OM stabilization, and in Ap horizons with high microbial activity and C turnover, organo‐mineral interactions can contribute to OM stabilization in the intermediate pool. The application of our model showed that we need a better understanding of processes causing spatial inaccessibility of OM to decomposers in the passive pool.  相似文献   

5.
Our understanding of the interactions between minerals, organic matter, and microorganisms at so-called biogeochemical interfaces in soil is still hampered by the inherent complexity of these systems. Artificial soil maturation experiments can help to bridge a gap in complexity between simple abiotic sorption experiments and larger-scale field experiments. By controlling other soil-forming factors, the effect of a particular variable can be identified in a simplified system. Here, we review the findings of a series of artificial soil incubation experiments with the aim of revealing general trends and conclusions. The artificial soils were designed to determine the effect of mineral composition and charcoal presence on the development of abiotic and biotic soil properties during maturation. In particular, the development of soil aggregates, organic matter (OM) composition and turnover, sorption properties, and the establishment of microbial community composition and function were considered. The main objectives of the research were to determine (1) how surface properties and sorption of chemicals modify biogeochemical interfaces; (2) how much time is required to form aggregates from mixtures of pure minerals, OM, and a microbial inoculum; and (3) how the presence of different mineral and charcoal surfaces affects aggregation, OM turnover, and the development of microbial community composition.  相似文献   

6.
An essential prerequisite for a sustainable soil use is to maintain a satisfactory soil organic‐matter (OM) level. This might be achieved by sound fertilization management, though impacts of fertilization on OM have been rarely investigated with the aid of physical fractionation techniques in semiarid regions. This study aimed at examining changes in organic C (OC) and N concentrations of physically separated soil OM pools after 26 y of fertilization at a site of the semiarid Loess Plateau in China. To separate sensitive OM pools, total macro‐OM (> 0.05 mm) was obtained from bulk soil by wet‐sieving and then separated into light macro‐OM (< 1.8 g cm–3) and heavy macro‐OM (> 1.8 g cm–3) subfractions; bulk soil was also differentiated into light OM (< 1.8 g cm–3) and mineral‐associated OM (> 1.8 g cm–3). Farmyard manure increased concentrations of total macro‐OC and N by 19% and 25%, and those of light fraction OC and N by 36% and 46%, compared to no manuring; both light OC and N concentrations but only total macro‐OC concentration responded positively to mineral fertilizations compared to no mineral fertilization. This demonstrated that the light‐fraction OM was more sensitive to organic or inorganic fertilization than the total macro‐OM. Mineral‐associated OC and N concentrations also increased by manuring or mineral fertilizations, indicating an increase of stable OM relative to no fertilization treatment, however, their shares on bulk soil OC and N decreased. Mineral fertilizations improved soil OM quality by decreasing C : N ratio in the light OM fraction whereas manuring led to a decline of the C : N ratio in the total macro‐OM fraction, with respect to nil treatment. Further fractionation of the total macro‐OM according to density clarified that across treatments about 3/4 of total macro‐OM was associated with minerals. Thus, by simultaneously applying particle‐size and density separation procedures, we clearly demonstrated that the macro‐OM differed from the light OM fraction not only in its chemical composition but also in associations with minerals. The proportion of the 0.5–0.25 mm water‐stable aggregates of soil was higher under organic or inorganic fertilizations than under no manure or no mineral fertilization, and increases in OC and N concentrations of water‐stable aggregates as affected by fertilization were greater for 1–0.5 and 0.5–0.25 mm classes than for the other classes. Results indicate that OM stocks in different soil pools can be increased and the loose aggregation of these strongly eroded loess soils can be improved by organic or inorganic fertilization.  相似文献   

7.
In the clay‐illuvial horizons (Bt) of Luvisols, surfaces of biopores and aggregates can be enriched in clay and organic matter (OM), relative to the bulk of the soil matrix. The OM composition of these coatings determines their bio‐physico‐chemical properties and is relevant for transport and transformation processes but is largely unknown at the molecular scale. The objective of this study was to improve the interpretation of spectra from Fourier transform infrared spectroscopy in diffuse reflectance mode (DRIFT) by using thermograms and released ion intensities obtained with pyrolysis‐field ionization mass spectrometry (Py‐FIMS) for a more detailed analysis of the mm‐scale spatial distribution of OM components at intact structural surfaces. Samples were separated from earthworm burrow walls, crack coatings, uncoated cracks, root channels, and pinhole fillings of the Bt‐horizons of Luvisols. The information from Py‐FI mass spectra enabled the assignment of OM functional groups also from spectral regions of overlapping DRIFT signal intensities to specific OM compound classes. In particular, bands from C=O and C=C bonds in the infrared range of wave numbers between 1,641 and 1,605 cm?1 were related to heterocyclic N‐compounds, benzonitrile, and naphthalene. The OM at earthworm burrow walls was composed of chemically labile aliphatic C‐rich and rather stable lignin and alkylaromatic compounds whereas the OM of thick crack coatings and pinholes was dominated by heterocyclic N and nitriles and high‐molecular compounds, likely originating from combustion residues. In combination with Py‐FIMS, DRIFT applications to intact samples seem promising for generating a more detailed mm‐scale spatial distribution of OM‐related sorption and wettability properties of crack and biopore surfaces that may serve as preferential flow paths in structured soils.  相似文献   

8.
Soil organic matter (OM) stabilization by the mineral phase can take place through sorption and aggregation. In this study we examined both of these processes, (i) organic carbon (OC) sorption onto clay‐sized particles and (ii) OC occlusion in silt‐size aggregates, with the objective of evaluating their relative importance in OM storage and stabilization in soil. We studied two loamy soil profiles (Haplic Luvisol and Plinthic Cambisol) currently under agricultural use down to a depth of 2 m. Our approach was based on two parallel fractionation methods using different dispersion intensities; these methods isolated a free clay fraction (non‐occluded) and a clay fraction occluded within water‐stable silt‐size aggregates. The two clay fractions were analysed for their C content and 14C activity. The proportion of sorbed OC was estimated as OC loss after hydrofluoric acid (HF) demineralization. Our results showed an important contribution to SOM stabilization by occlusion of OC into silt‐size aggregates with depth through both soil profiles. In the Haplic Luvisol, OC associated with clay and located in silt‐size aggregates accounted for 34–64% of the total soil OC, whereas in the Plinthic Cambisol this occluded material represented 34–40% of total OC. In the Haplic Luvisol, more OC was located in silt‐size aggregates than was sorbed onto clay‐size minerals, suggesting that silt‐size aggregation plays a dominant role in OC storage in this soil. In the Plinthic Cambisol, the abundance of sorbed OC increased with depth and contributed more to the stored C than that associated with silt‐size aggregates. Radiocarbon dating of both clay fractions (either occluded within silt‐size aggregates or not) suggests, in the case of the Plinthic Cambisol, a preferential stabilization of OC within silt‐size aggregates.  相似文献   

9.
Mechanisms for C stabilization in soils have received much interest recently due to their relevance in the global C cycle. Here we review the mechanisms that are currently, but often contradictorily or inconsistently, considered to contribute to organic matter (OM) protection against decomposition in temperate soils: (i) selective preservation due to recalcitrance of OM, including plant litter, rhizodeposits, microbial products, humic polymers, and charred OM; (ii) spatial inaccessibility of OM against decomposer organisms due to occlusion, intercalation, hydrophobicity and encapsulation; and (iii) stabilization by interaction with mineral surfaces (Fe‐, Al‐, Mn‐oxides, phyllosilicates) and metal ions. Our goal is to assess the relevance of these mechanisms to the formation of soil OM during different stages of decomposition and under different soil conditions. The view that OM stabilization is dominated by the selective preservation of recalcitrant organic components that accumulate in proportion to their chemical properties can no longer be accepted. In contrast, our analysis of mechanisms shows that: (i) the soil biotic community is able to disintegrate any OM of natural origin; (ii) molecular recalcitrance of OM is relative, rather than absolute; (iii) recalcitrance is only important during early decomposition and in active surface soils; while (iv) during late decomposition and in the subsoil, the relevance of spatial inaccessibility and organo‐mineral interactions for SOM stabilization increases. We conclude that major difficulties in the understanding and prediction of SOM dynamics originate from the simultaneous operation of several mechanisms. We discuss knowledge gaps and promising directions of future research.  相似文献   

10.
Traditionally, the selective preservation of certain recalcitrant organic compounds and the formation of recalcitrant humic substances have been regarded as an important mechanism for soil organic matter (SOM) stabilization. Based on a critical overview of available methods and on results from a cooperative research program, this paper evaluates how relevant recalcitrance is for the long‐term stabilization of SOM or its fractions. Methodologically, recalcitrance is difficult to assess, since the persistence of certain SOM fractions or specific compounds may also be caused by other stabilization mechanisms, such as physical protection or chemical interactions with mineral surfaces. If only free particulate SOM obtained from density fractionation is considered, it rarely reaches ages exceeding 50 y. Older light particles have often been identified as charred plant residues or as fossil C. The degradability of the readily bioavailable dissolved or water‐extractable OM fraction is often negatively correlated with its content in aromatic compounds, which therefore has been associated with recalcitrance. But in subsoils, dissolved organic matter aromaticity and biodegradability both are very low, indicating that other factors or compounds limit its degradation. Among the investigated specific compounds, lignin, lipids, and their derivatives have mean turnover times faster or similar as that of bulk SOM. Only a small fraction of the lignin inputs seems to persist in soils and is mainly found in the fine textural size fraction (<20 µm), indicating physico‐chemical stabilization. Compound‐specific analysis of 13C : 12C ratios of SOM pyrolysis products in soils with C3‐C4 crop changes revealed no compounds with mean residence times of > 40–50 y, unless fossil C was present in substantial amounts, as at a site exposed to lignite inputs in the past. Here, turnover of pyrolysis products seemed to be much longer, even for those attributed to carbohydrates or proteins. Apparently, fossil C from lignite coal is also utilized by soil organisms, which is further evidenced by low 14C concentrations in microbial phospholipid fatty acids from this site. Also, black C from charred plant materials was susceptible to microbial degradation in a short‐term (60 d) and a long‐term (2 y) incubation experiment. This degradation was enhanced, when glucose was supplied as an easily available microbial substrate. Similarly, SOM mineralization in many soils generally increased after addition of carbohydrates, amino acids, or simple organic acids, thus indicating that stability may also be caused by substrate limitations. It is concluded that the presented results do not provide much evidence that the selective preservation of recalcitrant primary biogenic compounds is a major SOM‐stabilization mechanism. Old SOM fractions with slow turnover rates were generally only found in association with soil minerals. The only not mineral‐associated SOM components that may be persistent in soils appear to be black and fossil C.  相似文献   

11.
Clay minerals have a major role in soil aggregation because of their large specific surface area and surface charges, which stimulate interactions with other mineral particles and organic matter. Soils usually contain a mixture of clay minerals with contrasting surface properties. Although these differences should result in different abilities of clay minerals regarding aggregate formation and stabilization, the role of different clay minerals in aggregation has been seldom evaluated. In this study, we took advantage of the intrinsic mineral heterogeneity of a temperate Luvisol to compare the role of clay minerals in aggregation. First, grassland and tilled soil samples were separated in water into aggregate‐size classes based on the aggregate hierarchy model. Then, clay mineralogy and organic C in the aggregate‐size classes were analysed. Interstratified minerals containing swelling phases accumulated in aggregated fractions compared with free clay fractions under the two land‐uses. The accumulation increased with decreasing aggregate size from large macroaggregates (> 500 µm) to microaggregates (50–250 µm). Carbon content and carbon‐to‐nitrogen ratio followed the opposite trend. This fully supports the aggregate hierarchy model, which postulates an increasing importance of mineral reactivity in smaller aggregates than in larger aggregates in which the cohesion relies mostly on physical enmeshment by fungal hyphae or small roots. Consequently, differences in the proportion of the different 2:1 clay minerals in soils can influence their structure development. Further research on the links between clay mineralogy and aggregation can improve our understanding of mechanisms of soil resistance to erosion and organic matter stabilization.  相似文献   

12.
Soil wettability is especially important for rainfed agriculture in climates with a dry period during the growing season. The effect of aggregate structure and soil organic C content on wettability of soil aggregates was determined for grassland (grass) and tilled fields (tillage). Soil organic C, plastic limit, aggregate total porosity, and wettability at 100 mm (rapid wetting) and 300 mm (slow wetting) water tension were measured on soil at 0–0.2 m depth. Natural aggregates from tillage and grass were compared to soil pellets formed by remolding aggregates. At both tensions, wettability of grass aggregates was significantly greater than that of tillage aggregates (P ≤ 0.001). Pellets were significantly less wettable than natural aggregates at 300 mm tension and during the initial wetting at 100 mm tension, but became significantly more wettable with time at 100 mm tension. Cumulative water uptake during 60 min exceeded the initial total porosity of pellets and natural tillage aggregates, suggesting incipient failure (formation of microcracks) during fast wetting. Grass aggregates contained twice as much organic C as tillage aggregates (26 g kg−1 versus 13 g kg−1). Organic C was linearly and positively related to plastic limit, total porosity, and the wettability of natural aggregates at 300 mm tension. At 100 mm tension, organic C was negatively related to wettability of natural aggregates under grass, but unrelated to wettability under tillage. Aggregate wettability was positively related to organic carbon content, except when the arrangement of soil constituents reduced or prevented incipient failure and soil dispersion during rapid wetting resulted in cumulative water uptake (60 min) similar to initial aggregate total porosity. Organic C increased wettability of grass aggregates when compared to tillage aggregates and also stabilized natural aggregates during fast wetting (100 mm tension). Both soil organic C content and aggregate structure were key factors controlling aggregate stability and wettability.  相似文献   

13.
土壤理化性质异质性研究及其影响   总被引：2，自引：0，他引：2  
Structured soils are characterized by the presence of inter- and intra-aggregate pore systems and aggregates, which show varying chemical, physical, and biological properties depending on the aggregate type and land use system. How far these aspects also affect the ion exchange processes and to what extent the interaction between the carbon distribution and kind of organic substances affect the internal soil strength as well as hydraulic properties like wettability are still under discussion. Thus, the objective of this research was to clarify the effect of soil aggregation on physical and chemical properties of structured soils at two scales： homogenized material and single aggregates. Data obtained by sequentially peeling off soil aggregates layers revealed gradients in the chemical composition from the aggregate surface to the aggregate core. In aggregates from long term untreated forest soils we found lower amounts of carbon in the external layer, while in arable soils the differentiation was not pronounced. However, soil aggregates originating from these sites exhibited a higher concentration of microbial activity in the outer aggregate layer and declined towards the interior. Furthermore, soil depth and the vegetation type affected the wettability. Aggregate strength depended on water suction and differences in tillage treatments.  相似文献   

14.
微生物残体在土壤中的积累转化过程与稳定机理研究进展   总被引：3，自引：0，他引：3  
张彬  陈奇  丁雪丽  何红波  张旭东 《土壤学报》2022,59(6):1479-1491
近年来,关于微生物残体在土壤有机质积累和转化过程中的作用越来越受到研究者的关注。土壤有机质中微生物残体的数量和组成比例变化与土壤有机质的形成、容量大小及周转特征密切相关。对目前土壤微生物残体研究方面的相关进展进行了梳理和总结,在明确土壤微生物残体的来源及其重要性的基础上,介绍了土壤微生物残体定量和转化的表征方法,阐述了微生物残体在土壤有机质积累转化过程中的作用及其主要影响因素,探讨了微生物残体在土壤中的稳定机制,提出了微生物通过同化代谢作用驱动细胞残体积累进而促进土壤有机质积累和稳定过程中亟待探讨的科学问题。期望为进一步探究陆地生态系统土壤有机质周转与微生物过程的相互作用机理提供一定的思考。  相似文献   

15.
Dissolved organic matter (DOM) is often considered the most labile portion of organic matter in soil and to be negligible with respect to the accumulation of soil C. In this short review, we present recent evidence that this view is invalid. The stability of DOM from forest floor horizons, peats, and topsoils against microbial degradation increases with advanced decomposition of the parent organic matter (OM). Aromatic compounds, deriving from lignin, likely are the most stable components of DOM while plant‐derived carbohydrates seem easily degradable. Carbohydrates and N‐rich compounds of microbial origin produced during the degradation of DOM can be relatively stable. Such components contribute much to DOM in the mineral subsoil. Sorption of DOM to soil minerals and (co‐)precipitation with Al (and probably also with Fe), especially of the inherently stable aromatic moieties, result in distinct stabilization. In laboratory incubation experiments, the mean residence time of DOM from the Oa horizon of a Haplic Podzol increased from <30 y in solution to >90 y after sorption to a subsoil. We combined DOM fluxes and mineralization rate constants for DOM sorbed to minerals and a subsoil horizon, and (co‐)precipitated with Al to estimate the potential contribution of DOM to total C in the mineral soil of a Haplic Podzol in Germany. The contribution of roots to DOM was not considered because of lack of data. The DOM‐derived soil C ranges from 20 to 55 Mg ha–1 in the mineral soil, which represents 19%–50% of the total soil C. The variation of the estimate reflects the variation in mineralization rate constants obtained for sorbed and (co‐)precipitated DOM. Nevertheless, the estimates indicate that DOM contributes significantly to the accumulation of stable OM in soil. A more precise estimation of DOM‐derived C in soils requires mineralization rate constants for DOM sorbed to all relevant minerals or (co‐)precipitated with Fe. Additionally, we need information on the contribution of sorption to distinct minerals as well as of (co‐)precipitation with Al and Fe to DOM retention.  相似文献   

16.
Biogeochemical mechanisms at microscale regions within soil macroaggregates strengthen aggregates during repeated DW cycles. Knowledge of additional biogeochemical processes that promote the movement of dissolved organic carbon (DOC) into and throughout soil aggregates and soil aggregate stabilization are essential before we can more accurately predict maximum carbon (C) sequestration by soils subjected to best management practices. We investigated the spatial distribution of 13C-glucose supplied to individual soil macroaggregate surfaces and subjected to multiple drying and wetting (DW) cycles. Subsequent distribution of added glucose-C, CO2 respiration, increased microbial community activity and concomitant changes in soil aggregate stabilization were monitored. Moist macroaggregates were treated with no DW cycles and zero glucose C (Control), 5 DW cycles and zero glucose (DW0G), and 5 DW cycles with additions of 250 μg glucose-13C/g soil during each cycle (DW+G). Repeated additions of glucose-C to aggregate surfaces reduced the mineralization of pre-existing soil C by an average of 45% and established concentric gradients of glucose-derived C. It is concluded these increasing gradients promoted the diffusion of soluble C into interior regions and became less available to microbial respiration. Spatial gradients of glucose-derived C within aggregates influenced a shift in the abundance of unique ribotypes spatially distributed within aggregates. Rapid decreases in the mineralization rates of glucose-C during repeated DW cycles suggested greater C sequestration by either physical restriction of microbes or chemical sorption of new C that diffused into aggregates. Aggregate stability decreased significantly following 2-3 DW cycles, when glucose-C was not added. Additions of glucose-C with each DW cycle maintained soil aggregate stability equal to the moist but not cycled control throughout the 5 DW cycles of this study. These data simulate the strengthening of soil aggregates in no tillage agroecosystems which provides continuous additions of DOC compounds generated by decomposing plant residues on the soil surface, and root exudates and decomposition, as well as the mineralization of POM materials within nondisturbed soil profiles.  相似文献   

17.
土壤有机碳稳定性影响因素的研究进展   总被引：12，自引：0，他引：12  
增加土壤碳汇是应对全球气候变化的有效措施,作为土壤碳汇来源之一的有机碳在其中发挥重要作用。过去几十年,土壤有机碳的分子结构性质被认为是预测有机碳在土壤中循环的主要标准。然而最近的研究结果表明有机碳的分子结构并非绝对地控制着土壤有机碳的稳定,而土壤环境因子与有机碳的相互作用显著降低了土壤有机碳被降解的可能性。土壤微生物不仅参与有机碳的降解,其产物本身也是土壤有机碳的重要组成成分。非生物因子直接或间接地控制着土壤有机碳的稳定,包括土壤中的无机颗粒、无机环境以及养分状况等。其中,有机碳与土壤矿物的吸附作用和土壤团聚体的闭蓄作用被普遍认为高效地保护了有机碳。土壤矿物的吸附作用取决于其自身的矿物学性质和有机碳的化学性质。土壤团聚体在保护有机碳的同时也促进了有机碳与矿物的吸附,而有机-矿物络合物同样可以参与形成团聚体。此外,土壤无机环境也影响着有机碳循环。总之,土壤有机碳的稳定取决于有机碳与周围环境的相互作用。同时,有机碳的结构性质也受控于环境因素。然而,无论有机碳的结构性质,还是其所处的生物与非生物环境,都是生态系统的基本属性,且各属性间相互影响、相互作用。因此,土壤有机碳的稳定是生态系统的一种特有性质。  相似文献   

18.
Water repellency is influenced by soil management and biological process. We carried out a 60‐day laboratory incubation experiment to evaluate the effects of straw amendment, together with the intensity and frequency of wetting and drying (W/D), on microbial processes and water repellency. One W/D cycle consisted of 1.5‐day wetting at −0.03 kPa from the soil core bottom and different drying lengths in a temperature‐controlled laboratory, resulting in different drying intensities. At a regular interval, soil respiration rate (SRR) on drying and wetting, soil microbial biomass C and N (SMB‐C and N), and soil water repellency (SWR) after the wetting were measured simultaneously. Rice straw amendment had a greater effect on SRR, but smaller influences on SMB and SMB‐C : N than W/D frequency and drying intensity. The first W/D caused the largest decrease in soil respiration and the soil respiration recovered partly in the subsequent W/D cycles. The increase in SMB and SMB‐C : N as well as metabolic quotient with W/D frequency and intensity suggested a shift of microbial community from bacterial dominance to fungal dominance. SWR was significantly related to SMB‐C (R2= 0.689, P < 0.001). However, this study was limited to these indirect measurements. Direct measurements of fungal biomass and microbial community are needed in the future. The results suggest that rice straw amendment in dry season may increase C sequestration due to reduced decomposition and stabilize soil structure due to the enhancement of microbial induced water repellency.  相似文献   

19.
Naturally occurring wetting‐and‐drying cycles often enhance aggregation and give rise to a stable soil structure. In comparatively dry regions, such as large areas of Australia, organic‐matter (OM) contents in topsoils of arable land are usually small. Therefore, the effects of wetting and drying are almost solely reliant on the clay content. To investigate the relations between wetting‐and‐drying cycles, aggregation, clay content, and OM in the Australian environment, an experiment was set up to determine the relative influence of both clay content (23%, 31%, 34%, and 38%) and OM amendments of barley straw (equivalent to 3.1 t ha–1, 6.2 t ha–1, and 12.4 t ha–1) on the development of water‐stable aggregates in agricultural soil. The aggregate stability of each of the sixteen composite soils was determined after one, three, and six wet/dry cycles and subsequent fast and slow prewetting and was then compared to the aggregate stabilities of all other composite soils. While a single wet/dry cycle initiated soil structural evolution in all composite soils, enhancing macroaggregation, the incorporation of barley straw was most effective for the development of water‐stable aggregates in those soils with 34% and 38% clay. Repeated wetting‐and‐drying events revealed that soil aggregation is primarily based on the clay content of the soil, but that large straw additions also tend to enhance soil aggregation. Relative to untreated soil, straw additions equivalent to 3.1 t ha–1 and 12.4 t ha–1 increased soil aggregation by about 100% and 250%, respectively, after three wet/dry cycles and fast prewetting, but were of less influence with subsequent wet/dry cycles. Straw additions were even more effective in aggregating soil when combined with slow prewetting; after three wet/dry cycles, the mean weight diameters of aggregates were increased by 70% and 140% with the same OM additions and by 160% and 290% after six wet/dry cycles, compared to samples without organic amendments. We suggest that in arable soils poor in OM and with a field texture grade of clay loam or finer, the addition of straw, which is often available from preceding crops, may be useful for improving aggregation. For a satisfactory degree of aggregate stability and an improved soil structural form, we found that straw additions of at least 6.2 t ha–1 were required. However, rapid wetting of straw‐amended soil will disrupt newly formed aggregates, and straw has only a limited ability to sustain structural improvement.  相似文献   

20.
Permafrost degradation may cause strong feedbacks of arctic ecosystems to global warming, but this will depend on if, and to what extent, organic matter (OM) is protected against biodegradation by mechanisms other than freezing and anoxia. Here, we report on the amount, chemical composition and bioavailability of particulate (POM) and mineral‐associated OM (MOM) in permafrost soils of the East Siberian Arctic. The average total organic carbon (OC) stock across all soils was 24.0 ± 6.7 kg m?2 within 100 cm soil depth. Density fractionation (density cut‐off 1.6 g cm?3) revealed that 54 ± 16% of the total soil OC and 64 ± 18% of OC in subsoil horizons was bound to minerals. As well as sorption of OM to clay‐sized minerals (R2 = 0.80; P < 0.01), co‐precipitation of OM with hydrolyzable metals may also transfer carbon into the mineral‐bound fraction. Carbon:nitrogen ratios, stable carbon and nitrogen isotopes, 13C‐NMR and X‐ray photoelectron spectroscopy showed that OM is transformed in permafrost soils, which is a prerequisite for the formation of mineral‐organic associations. Mineral‐associated OM in deeper soil was enriched in 13C and 15N, and had narrow C:N and large alkyl C:(O‐/N‐alkyl C) ratios, indicating an advanced stage of decomposition. Despite being up to several thousands of years old, when incubated under favourable conditions (60% water‐holding capacity, 15°C, adequate nutrients, 90 days), only 1.5–5% of the mineral‐associated OC was released as CO2. In the topsoils, POM had the largest mineralization but was even less bioavailable than the MOM in subsoil horizons. Our results suggest that the formation of mineral‐organic associations acts as an important additional factor in the stabilization of OM in permafrost soils. Although the majority of MOM was not prone to decomposition under favourable conditions, mineral‐organic associations host a readily accessible carbon fraction, which may actively participate in ecosystem carbon exchange.  相似文献   

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