Photodegradation effects on CO2 emissions from litter and SOM and photo-facilitation of microbial decomposition in a California grassland

Decomposition of soil organic matter (SOM) and plant litter has been shown to be affected by high solar radiation; this could partly explain why biogeochemical models underestimate decomposition in arid and semi-arid ecosystems. We set out to test the effect of using traditional PVC chambers for measuring soil gas fluxes versus quartz chambers that allowed passage of light during field measurements in a dry-land field in Davis, CA. Results showed that fluxes from quartz-top chambers were on average 29% higher than from opaque chambers. We also studied the effect of solar light exposure on decomposition of native grass litter and SOM in a field experiment where plots were shaded or left exposed for 157 days during summer; litter did not seem to be affected by exposure to light. However, we concluded that SOM decomposition was affected by light exposure since shaded soil had similar respiration to sunlight-exposed soil indicating that microbial respiration occurred under the shade while photo-degradation likely occurred under the sun. Additionally, ¹⁵N-labeled grass was placed in litter bags in the field with either clear filters to allow light or aluminum covers to block light; 3-month exposure caused a change in lignin degradability as indicated by the change in the Ad/Al ratio. Incubation of that litter showed 9.3% more CO₂ produced from litter in clear and aluminum bags than unexposed litter. This showed that photo-facilitation occurred although to a small degree and was a result of light exposure and/or heat degradation. We attributed the similar respiration from clear- and aluminum-exposed litter to heat degradation of the aluminum-exposed litter. In conclusion, our results show that in hot dry ecosystems conventional PVC chambers underestimate measured CO₂ flux rates; sunlight exposure changes litter chemistry and appears to affect the degradation of soil organic matter, but the magnitude of degradation depends on an interaction of factors such as soil temperature and moisture.     

Microbial processes controlling P availability in forest spodosols as affected by soil depth and soil properties

Because carbon dioxide (CO₂) concentration is rising, increases in plant biomass and productivity of terrestrial ecosystems are expected. However, phosphorus (P) unavailability may disable any potential enhanced growth of plants in forest ecosystems. In response to P scarcity under elevated CO₂, trees may mine deeper the soil to take up more nutrients. In this scope, the ability of deep horizons of forest soils to supply available P to the trees has to be evaluated. The main objective of the present study was to quantify the relative contribution of topsoil horizons and deep horizons to P availability through processes governed by the activity of soil micro-organisms. Since soil properties vary with soil depth, one can therefore assume that the role of microbial processes governing P availability differs between soil layers. More specifically, our initial hypothesis was that deeper soil horizons could substantially contribute to total plant available P in forested ecosystems and that such contribution of deep horizons differs among sites (due to contrasting soil properties). To test this hypothesis, we quantified microbial P and mineralization of P in ‘dead’ soil organic matter to a depth of 120 cm in forest soils contrasting in soil organic matter, soil moisture and aluminum (Al) and iron (Fe) oxides. We also quantified microbiological activity and acid phosphomonoesterase activity. Results showed that the role of microbial processes generally decreases with increasing soil depth. However, the relative contribution of surface (litter and 0–30 cm) and deep (30–120 cm) soil layers to the stocks of available P through microbial processes (51–62 kg P ha^?1) are affected by several soil properties, and the contribution of deep soil layers to these stocks vary between sites (from 29 to 59%). This shows that subsoils should be taken into account when studying the microbial processes governing P availability in forest ecosystems. For the studied soils, microbial P and mineralization of P in ‘dead’ soil organic matter particularly depended on soil organic matter content, soil moisture and, to a minor extent, Al oxides. High Al oxide contents in some sites or in deep soil layers probably result in the stabilization of soil organic compounds thus reducing microbiological activity and mineralization rates. The mineralization process in the litter also appeared to be P-limited and depended on the C:P ratio of soil organic matter. Thus, this study highlighted the effects of soil depth and soil properties on the microbial processes governing P availability in the forest spodosols.     

氮输入对森林土壤有机碳截存与损耗过程的影响

大气氮沉降对受氮限制的陆地生态系统碳截存/损耗的机理尚不清楚,尤其是对土壤有机碳(SOC)的输入、转化和输出过程的认识明显不足。本文论述了外源性氮素(氮沉降、人为增氮)对凋落物分解、土壤有机碳各组分周转的影响,以及土壤呼吸各组分(根系自养呼吸、根际微生物呼吸和SOM分解)对增氮的响应等领域的最新研究进展,指出了在上述研究领域中存在的问题,并提出拟解决的途径以及未来的可能研究方向,以期为该领域的研究提供参考。     

Effects of litter addition and warming on soil carbon, nutrient pools and microbial communities in a subarctic heath ecosystem

Climatic warming leads to the expansion of deciduous shrubs and trees in the Arctic. This leads to higher leaf litter inputs, which together with warming may alter the rate of carbon and nutrient cycling in the arctic ecosystems. We assessed effects of factorial warming and additional litter on the soil ecosystem of a subarctic heath in a 7-year-long field experiment. Fine root biomass, dissolved organic carbon (DOC) and total C concentration increased in response to warming, which probably was a result of the increased vegetation cover. Litter addition increased the concentration of inorganic P in the uppermost 5 cm soil, while decreasing the pool of total P per unit area of the organic profile and having no significant effects on N concentrations or pools. Microbial biomass C and N were unaffected by the treatments, while the microbial biomass P increased significantly with litter addition. Soil ergosterol concentration was also slightly increased by the added litter in the uppermost soil, although not statistically significantly. According to a principal component analysis of the phospholipid fatty acid profiles, litter addition differed from the other treatments by increasing the relative proportion of biomarkers for Gram-positive bacteria. The combined warming plus litter addition treatment decreased the soil water content in the uppermost 5 cm soil, which was a likely reason for many interactions between the effects of warming and litter addition. The soil organic matter quality of the combined treatment was also clearly different from the control based on a near-infrared reflectance (NIR) spectroscopic analysis, implying that the treatment altered the composition of soil organic matter. However, it appears that the biological processes and the microbial community composition responded more to the soil and litter moisture conditions than to the change in the quality of the organic matter.     

Parameters of the productivity of soil algae in terrestrial ecosystems

A review is presented of the recent state of the problem of soil algae productivity in terrestrial ecosystems on the basis of literature data and our own research. It is shown that the organic matter accumulated by soil algae is highly mobile. The following parameters were analyzed: the biological production, the time of the biomass turnover, and the rate of the algal organic matter renewal in the soil. The average monthly production of algae ranged from 0.9 to 765 g/m², the rate of the organic matter renewal ranged from 0.03 to 25.5 g/m² per day, and the time of the algal biomass renewal ranged from 0.1 to 7 days.     

外源氮输入对土壤有机碳矿化和凋落物分解的影响

目前,由人类活动造成的陆地生态系统氮输入量已经远远超过了其自身的生物固氮,外源氮输入的增多已经并将继续对土壤有机碳矿化和凋落物分解产生影响。本文分析了国内外有关氮输入增多对土壤有机碳矿化和凋落物分解的影响及其机理:由于研究点环境状况不同,凋落物性质的差异和分解阶段的不同等原因,氮输入对土壤有机碳矿化的结果主要表现为抑制或促进作用;对凋落物分解的影响表现为促进、无影响和抑制三种效果,有关其作用机理还有待进一步深入研究。着重指出对于作为大气CO2"汇"的沼泽湿地,氮输入的增多能够对其碳"汇"功能产生影响,因此进行氮输入对湿地土壤有机碳矿化和凋落物分解方面的研究,对于探讨湿地碳循环对外源氮输入的响应及其机理非常重要。     

Effects of liming on organic matter decomposition and phosphorus extractability in an acid humic Ranker soil from northwest Spain

Summary A laboratory incubation experiment was carried out over 17 weeks to determine the effect of liming on soil organic matter. The amount of lime as calcium hydroxide [Ca(OH)₂] required to completely neutralise exchangeable Al was found to be five times the standard lime requirement. This large amount of lime had a limited overall effect on the short-term stability of soil organic matter, causing the release of 1300 g g^-1 of C (1.7% total soil C) above the control during the incubation. Liming may have altered the potential availability of soil organic matter and organic P, as shown by a marked reduction in the extractability of soil organic P with sodium bicarbonate and sodium hydroxide. The latter was unlikely to be due to the formation of calclium-P artefacts, and may be attributed to the combined chemical effects of added calcium hydroxide and precipitation of exchangeable Al on the nature and solubility of soil organic constituents and organomineral complexes. The addition of lime increased the degradation of added oak leaf litter by 50%, from 3.2 to 4.7 mg g^-1, as determined by CO₂ evolution. The enhanced litter degradation indicated increased microbial activity in limed soil, but this improvement had only minor effects on the stability of native organic matter. This study highlights the need for further research into the relationships between the chemical nature of organic P in soil and the physical, chemical, temporal, and agronomic factors that control its turnover and availability.     

Previous exposure advances the degradation of an anthropogenic s-triazine regardless of soil origin

Purpose

Previous investigations—field samplings and laboratory experiments—support the hypothesis that the degradation of s-triazines is enhanced in previously exposed as compared to pristine soils in terrestrial environments. Despite this, bottlenecks of soil sampling and various soil modification practices in microcosm studies have made it difficult to guarantee that previous contamination history enhances contaminant degradation regardless of soil origin in terrestrial ecosystems. We test the hypothesis that the degradation of simazine (2-chloro-4,6-bis(ethylamino)-s-triazine) is enhanced in previously exposed soils as compared to pristine soils in 10 l buckets at the mesocosm scale.

Materials and methods

We collected soil at three separate sites consisting of a previously exposed and a pristine field. At every field, soil was collected at three separate plots and simazine degradation (days 0 and 65) and the response to atzB degrader gene primers (days 0 and 110) were followed. We analyzed the results using analysis of covariance (ANCOVA). Previous exposure and field site were assessed as fixed factors and initial simazine concentration and abiotic soil conditions as covariates.

Results and discussion

After the 65-day exposure, remaining simazine concentrations depended on previous exposure but not on collection site. The response to atzB gene primers was positive in all mesocosms where simazine degradation had been rapid. Soil moisture, pH, and organic matter content were insignificant. If soil moisture was not included in the ANCOVA model, previous exposure did not appear as a significant factor.

Conclusions

The results support the hypothesis that simazine is degraded more rapidly in previously exposed soils as compared to pristine environments, provided that degradation genes are available. Previously exposed soil might be used to enhance the degradation of simazine in recently contaminated terrestrial soils, supposing that the central requirements for microbial growth are adequate.     

Volatile organic compound (VOC) emissions from soil and litter samples

The production of nonmethane volatile organic compounds (VOCs) by soil microbes is likely to have an important influence on soil ecology and terrestrial biogeochemistry. However, soil VOC production has received relatively little attention, and we do not know how the emissions of microbially-produced VOCs vary across soil and litter types. We collected 40 root-free soil and litter samples from a diverse array of ecosystem types and conducted laboratory incubations in order to compare the types and quantities of VOCs emitted. VOC production rates were higher in litter samples than in soil samples, and the rates were correlated with microbial biomass and CO₂ production levels. On average, the litter samples produced more types of VOCs than the soil samples with litters emitting a number of VOCs (including terpenoids) that were not generally emitted from the soil samples. Across all of the samples, we identified 100 VOCs, and more than 70% of these compounds could not be positively identified by GC/MS analyses. Of those VOCs that could be identified, furfural and similar furan compounds were noteworthy in that they were emitted in large amounts from nearly every sample examined. Other identifiable VOCs produced across a range of soil and litter samples included propanoic and butanoic acids, which are known products of microbial fermentation. Together these results suggest a need for additional research examining the specific factors influencing VOC emissions from soil and the identification of specific VOCs emitted from soil and litter as many of these compounds are likely to have important effects on belowground ecology.     

人工杉木林地有机物和养分库的退化与调控

研究表明,人工杉木林地土壤有机物和养分库严重退化,地表枯枝落叶层中干和各种养分的贮量与阔叶林和混交林比较明显下降,土壤中有机质,全Ｎ量和碱解Ｎ含量的剖面分布也表现出相同的趋势。传统的炼山造林使杉木林地枯枝落叶和养分库是呈突变形式 经,林份组成单一,凋落物数量和养分含和也是杉木林土壤有机物和归库退化的重要因素。通过改进林木更新方式和改善林份组成很大程度上控制人工林有机物和养分库的退化。     

丛枝菌根真菌介导的土壤有机碳稳定机制研究进展

土壤有机碳(SOC)的稳定是陆地生态系统碳循环的关键过程之一,对维持土壤肥力和减少温室气体排放具有重要意义。以往认为植物残体中难降解性物质的物理保护和腐殖质影响土壤中有机碳库的稳定性。最近的研究结果表明,微生物介导的碳循环过程在土壤有机碳稳定中发挥着重要作用。丛枝菌根真菌(arbuscular mycorrhizal fungi,AMF)作为土壤中一类重要的共生微生物,参与植物光合碳向土壤的转运和分配,是陆地生态系统碳循环的重要一环,但其在土壤有机碳稳定中的作用潜力还未得到充分挖掘。基于此,本文估算了植物光合碳在AMF根外菌丝的分配量;总结了AMF介导的土壤有机碳稳定机制,主要包括AMF活体菌丝对碳的截留,分泌物及残体的分子结构抗性和土壤矿物吸附,提高植物源碳的质量和数量,菌丝分泌物及残体的激发效应和稳定土壤团聚体;探讨了影响AMF介导的稳定性有机碳形成的非生物(气候因子、土壤养分和土壤矿物)和生物因子(植物和AMF种类);提出了AMF与土壤有机碳周转互作机理进一步的研究方向,包括探究菌根植物光合碳转化为稳定性SOC的机制,解析不同生态系统中AMF对稳定性SOC的贡献及影响因素,并厘清...     

植物凋落物分解对土壤有机碳稳定性影响的研究进展

凋落物是植物向土壤输入有机碳的主要途径,源于凋落物的碳一部分以CO₂的形式散失到大气,另一部分以有机碳的形式输入到土壤中,在土壤微生物的作用下经过一系列的周转参与稳定有机质的形成。但土壤作为“黑箱”,凋落物向土壤有机碳转移的过程和作用机理仍不明确。结合国内外该研究领域的主要成果,简要介绍了植物凋落物分解的研究方法、土壤有机碳组分及土壤有机碳稳定性,并从植物凋落物分解对土壤有机碳及其组分、土壤呼吸和激发效应、土壤微生物群落结构及酶活性的影响以及植物-土壤-微生物相互作用过程对有机碳稳定性的影响等方面进行概述,厘清植物凋落物分解与土壤稳定有机碳形成的关系,并提出了未来该领域亟待关注的研究方向和研究内容。     

Arbuscular mycorrhizal fungi contribute to C and N enrichment of soil organic matter in forest soils

Increasing evidence suggests that accretion of microbial turnover products is an important driver for isotopic carbon (C) and nitrogen (N) enrichment of soil organic matter (SOM). However, the exact contribution of arbuscular mycorrhizal fungi (AMF) to soil isotopic patterns remains unknown. In this study, we compared ¹³C and ¹⁵N patterns of glomalin-related soil protein (GRSP), which includes a main fraction derived from AMF, litter, and bulk soil in four temperate rainforests. GRSP was an abundant C and N pool in these forest soils, showing significant ¹³C and ¹⁵N enrichment relative to litter and bulk soil. Hence, cumulative accumulation of recalcitrant AMF turnover products in the soil profile likely contributes to ¹³C and ¹⁵N enrichment in forest soils. Further research on the relationship between GRSP and AMF should clarify the exact extent of this process.     

Temporal dynamics of iron-rich, tropical soil organic carbon pools after land-use change from forest to sugarcane

Background, aim, and scope  

Land-use change can significantly influence carbon (C) storage and fluxes in terrestrial ecosystems. Soil–plant systems can act as sinks or sources of atmospheric CO₂ depending on formation and decomposition rates of soil organic matter. Therefore, changes in tropical soil C pools could have significant impacts on the global C cycle. This study aims to evaluate the impacts of long-term sugarcane cultivation on soil aggregation and organic matter, and to quantify temporal dynamics of soil organic matter in cultivated sugarcane plantation soils previously under a tropical natural secondary forest.     

Analytical pyrolysis of a soil profile under Scots pine

The chemical properties of pine needle litter cause slow decomposition, which results in an accumulation of highly lignocellulosic material on the forest floor. Decomposition of organic matter is important for the nutrient turnover in pine forests on nutrient-poor soils. We studied the biodegradation of needles in an organic layer focusing on the various stages of lignin degradation by fungi. Samples were obtained from pine needle litter and a stratified organic layer over nutrient-poor sand under a 60-year-old Scots pine (Pinus sylvestris forest stand. Pyrolysis mass spectrometry (PyMS) and pyrolysis gas chromatography mass spectrometry (PyGCMS) were used to characterize the chemical composition of the needles and the soil. The pyrolysis data show that diterpenoid acids are a main component in fresh needles, but rapidly decrease in the organic layer of the soil, as a result of decomposition. The chemical composition of the soil profile is dominated by guaiacyl lignin and polysaccharides from needle litter. The hexose/pentose ratio increases with depth in the soil profile. The partial preservation of hexose polymers is the result of the preferential decomposition of pentose polymers by white-rot fungi, and points to the input of microbially synthesized polysaccharides. Indications for the degradation of guaiacyl lignin are also found in the soil profile. Oxidative reactions by soil fungi result in a shortening of the side chain of the guaiacyl lignin derivatives and an increase of carbonyl and carboxyl groups. These degradational patterns of lignin in the soil profile under Scots pine are similar to those observed in lignin model compounds and wood lignin degraded by fungi under controlled laboratory conditions.     

Physical fractionation of soil and structural and functional complexity in organic matter turnover

Physical fractionation is used increasingly to study the turnover of organic matter in soil. This essay links the methods of fractionation to concepts of turnover by defining levels of structural and functional complexity that refer to experimentally verifiable pools of organic matter in the soil. Physical fractionation according to size and density of soil particles emphasizes the importance of interactions between organic and inorganic soil components in the turnover of organic matter. It allows the separation of free and occluded uncomplexed organic matter and of primary and secondary organomineral complexes. This methodological approach recognizes that the overall regulation of decomposer activity is through the structure of soil, which determines gas exchange, the availability of substrates and water, and the transport of solutes. Results from physical fractionations suggest three levels of structural and functional complexity in the turnover of organic matter in soil. Primary organomineral complexes isolated from fully dispersed soil account for the primary level of complexity. The clay‐, silt‐ and sand‐sized complexes are seen as the basic units in soil, surface reactions between substrates, organisms and minerals being the main regulatory mechanisms. Secondary complexes reflect the degree of aggregation of primary organomineral complexes and refer to the second level of complexity. Physical protection of uncomplexed organic matter and soil organisms and the creation of gas and moisture gradients are emergent features regulating the turnover at this level of complexity. The structurally intact soil (the soil in situ) constitutes the third level of complexity. This integrates the effects of primary and secondary complexes. Emergent structural features associated with this level are resource islands, macropores, roots, mesofauna, tillage and soil compaction, the corresponding functional features being related to the transport and exchange of solutes and gases, and the spatial distribution and comminution of litter and uncomplexed organic matter. Thus, a thorough understanding of the turnover and storage of organic matter in soil can be acquired only by considering all levels of complexity in the decomposition subsystem.     

Phenol oxidase, peroxidase and organic matter dynamics of soil

Extracellular enzymes mediate the degradation, transformation and mineralization of soil organic matter. The activity of cellulases, phosphatases and other hydrolases has received extensive study and in many cases stoichiometric relationships and responses to disturbances are well established. In contrast, phenol oxidase and peroxidase activities, which are often uncorrelated with hydrolase activities, have been measured in only a small subset of soil enzyme studies. These enzymes are expressed for a variety of purposes including ontogeny, defense and the acquisition of carbon and nitrogen. Through excretion or lysis, these enzymes enter the environment where their aggegrate activity mediates key ecosystem functions of lignin degradation, humification, carbon mineralization and dissolved organic carbon export. Phenol oxidases and peroxidases are less stable in the environment than extracellular hydrolases, especially when associated with organic particles. Activities are also affected, positively and negatively, by interaction with mineral surfaces. High spatiotemporal variation obscures their relationships with environmental variables and ecological process. Across ecosystems, phenol oxidase and peroxidase activities generally increase with soil pH, a finding not predicted from the pH optima of purified enzymes. Activities associated with plant litter and particulate organic matter often correlate with decomposition rates and potential activities generally increase with the lignin and secondary compound content of the material. At the ecosystem scale, nitrogen amendment alters the expression of phenol oxidase and peroxidase enzymes more broadly than culture studies imply and these responses correlate with positive and negative changes in litter decomposition rates and soil organic matter content. At the global scale, N amendment of basidiomycete-dominated soils of temperate and boreal forest ecoystems often leads to losses of oxidative enzyme activity, while activities in grassland soils dominated by glomeromycota and ascomycetes show little net response. Land use that leads to loss of soil organic matter tends to increase oxidative activities. Across ecosystems, soil organic matter content is not correlated with mean potential phenol oxidase and peroxidase activities. A multiple regression model that includes soil pH, mean annual temperature, mean annual precipitation and potential phenol oxidase activity accounts for 37% of the variation in soil organic matter (SOM) content across ecosystems (n = 63); a similar model for peroxidase activity describes 32% of SOM variance (n = 43). Analysis of residual variation suggest that suites of interacting factors create both positive and negative feedbacks on soil organic matter storage. Soils with high oxygen availability, pH and mineral activity tend to be substrate limited: high in situ oxidative activities limit soil organic matter accumulation. Soils with opposing characteristics are activity limited: low in situ oxidative activities promote soil organic matter storage.     

Influence of organic by-products and nitrogen source on chemical and microbiological status of an agricultural soil

We assessed the influence of the addition of four municipal or agricultural by-products (cotton gin waste, ground newsprint, woodchips, or yard trimmings), combined with two sources of nitrogen (N), [ammonium nitrate (NH₄NO₃) or poultry litter] as carbon (C) sources on active bacterial, active fungal and total microbial biomass, cellulose decomposition, potential net mineralization of soil C and N and soil nutrient status in agricultural soils. Cotton gin waste as a C source promoted the highest potential net N mineralization and N turnover. Municipal or agricultural by-products as C sources had no affect on active bacterial, active fungal or total microbial biomass, C turnover, or the ratio of net C:N mineralized. Organic by-products and N additions to soil did not consistently affect C turnover rates, active bacterial, active fungal or total microbial biomass. After 3, 6 or 9 weeks of laboratory incubation, soil amended with organic by-products plus poultry litter resulted in higher cellulose degradation rates than soil amended with organic by-products plus NH₄NO₃. Cellulose degradation was highest when soil was amended with newsprint plus poultry litter. When soil was amended with organic by-products plus NH₄NO₃, cellulose degradation did not differ from soil amended with only poultry litter or unamended soil. Soil amended with organic by-products had higher concentrations of soil C than soil amended with only poultry litter or unamended soil. Soil amended with organic by-products plus N as poultry litter generally, but not always, had higher extractable P, K, Ca, and Mg concentrations than soil amended with poultry litter or unamende soil. Agricultural soil amended with organic by-products and N had higher extractable N, P, K, Ca and Mg than unamended soil. Since cotton gin waste plus poultry litter resulted in higher cellulose degradation and net N mineralization, its use may result in faster increase in soil nutrient status than the other organic by-products and N sources that were tested. Received: 15 May 1996     

Soil organic N - An under-rated player for C sequestration in soils?

The availability of Soil Organic Nitrogen (SON) determines soil fertility and biomass production to a great extent. SON also affects the amounts and turnover rates of the soil organic carbon (SOC) pools. Although there is increasing awareness of the impact of the nitrogen (N) cycle on the carbon (C) cycle, the extent of this interaction and the implications for soil organic matter (SOM) dynamics are still under debate. Therefore, present knowledge about the inter-relationships of the soil cycles of C and N as well as current ideas about SON stabilization are summarized in this paper in order to develop an advanced concept of the role of N on C sequestration. Modeling global C-cycling, it was already recognized that SON and SOC are closely coupled via biomass production and degradation. However, the narrow C/N ratio of mature soil organic matter (SOM) shows further that the impact of SON on the refractory SOM is beyond that of determining the size of the active cycling entities. It affects the quantity of the slow cycling pool and as a major contributor it also determines its chemical composition. Although the chemical nature of SON is still not very well understood, both improved classical wet chemical analyses and modern spectroscopic techniques provide increasing evidence that almost the entire organic N in fire-unaffected soils is bound in peptide-like compounds and to a lesser extent in amino sugars. This clearly points to the conclusion, that such compounds have greater importance for SOM formation than previously assumed. Based on published papers, I suggest that peptides even have a key function in the C-sequestration process. Although the mechanisms involved in their medium and long-term stabilization are far from understood, the immobilization of these biomolecules seems to determine the chemistry and functionality of the slow cycling SOM fraction and even the potential of a soil to act as a C sink. Pyrogenic organic N, which derives mostly from incomplete combustion of plant and litter peptides is another under-rated player in soil organic matter preservation. In fire-prone regions, its formation represents a major N stabilization mechanism, leading to the accumulation of heterocyclic aromatic N, the stability of which is still not elaborated. The concept of peptide-like compounds as a key in SOM-sequestration implies that for an improved evaluation of the potential of soils as C-sinks our research focus as to be directed to a better understanding of their chemistry and of the mechanisms which are responsible for their resistance against biochemical degradation in soils.     

稳定13C同位素示踪技术在农田土壤碳循环和团聚体 固碳研究中的应用进展

农田土壤有机碳库是全球碳循环的重要组成部分,其积累和分解直接影响陆地生态系统碳贮藏与全球碳平衡。土壤团聚体是土壤结构的物质基础和土壤肥力的重要载体,也是土壤有机碳的固定场所。稳定~(13)C同位素示踪技术是研究土壤碳动态变化的有效手段,能够揭示新输入碳在土壤及团聚体中赋存状态、周转过程以及微生物的调节机制。本文主要归纳与阐述了稳定~(13)C同位素示踪技术在农田土壤有机碳循环及土壤团聚体固碳机理方面的研究进展,提出~(13)C同位素示踪技术在未来土壤碳循环和固碳机制方面的主要研究方向。