Roles of shoots and roots in cadmium uptake and distribution in tubers of potato (<Emphasis Type="Italic">Solanum tuberosum</Emphasis> L)

Aims

We investigated whether density fractionation can be used to determine the distribution of organic phosphorus (OP) between free and mineral-associated soil organic matter (SOM).

Methods

We performed density fractionations using sodium polytungstate solution (specific gravity 1.6 g cm^?3) on 20 soils from UK semi-natural and pasture ecosystems, to obtain a light fraction (LF) and a heavy fraction (HF) for each soil. The fractions were quantified by weight, and analysed for organic carbon (OC), total N (TN), total P (TP), inorganic P (IP), and OP (by difference).

Results

Good recoveries of soil mass (96%), OC and TN (both ~ 90%) were obtained, but recovery of OP only averaged 56%. The average P:C ratio of HF SOM exceeded that of LF SOM by a factor of six, greater than the factor of two obtained for TN:OC. For the soils studied, the elements of SOM were predominantly in the HF, with averages of 75% for C, 82% for N, and 90% for P.

Conclusions

The incomplete recovery of OP demands further work. Nonetheless, the results show that HF SOM is much richer in P than LF SOM.

     

氮沉降增加情景下植物-土壤-微生物交互对自然生态系统土壤有机碳的调控研究进展

大气氮沉降增加倾向于促进受氮限制陆地生态系统地上生物量,但是对地下碳过程和土壤碳截存的影响结果迥异,导致陆地生态系统“氮促碳汇”的评估存在很大的不确定性。大气氮沉降输入直接影响微生物活性或间接影响底物质量,改变凋落物和土壤有机质(SOM)的分解速率和分解程度,进而影响土壤有机碳(SOC)的积累与损耗过程。过去相关研究主要集中在土壤碳转化过程和碳储量动态方面,缺乏植物-微生物-SOM交互作用的理解,对土壤碳截存调控的生物化学和微生物学机理尚不清楚。本文以地下碳循环过程为主线,分别综述了氮沉降增加对植物地下碳分配、SOC激发效应、微生物群落碳代谢过程的影响,深入分析SOM化学稳定性与微生物群落动态的关系。该领域研究的薄弱环节体现在:(1)增氮倾向于降低根系的生长和周转,对根际沉积碳分配(数量和格局)的影响及驱动因素不明确;(2)虽然认识到氮素有效性影响土壤激发效应的方向和强度,但是氧化态NO-3和还原态NH+4输入对有机质激发效应的差异性影响及潜在机理知之甚少;(3)微生物碳利用效率(CUE)是微生物群落碳代谢的关键表征,能够很好地解释土壤碳的积累与损耗过程;由于缺乏适宜的测定方法,难以准确量化土壤微生物的CUE及微生物生物量的周转时间;(4)增氮会抑制土壤真菌群落及其胞外酶活性,对细菌群落组成的影响尚未定论,有关SOM化学质量与土壤微生物群落活性、组成之间的耦合关系尚不清楚。未来研究应基于长期的氮添加控制实验平台,结合碳氧稳定性同位素示踪、有机质化学、分子生物学和宏基因组学等方法,深入分析植物同化碳的地下分配规律、微生物碳代谢和周转、有机质化学结构与功能微生物群落的耦合关系等关键环节。上述研究将有助于揭示植物-土壤-微生物交互作用对SOC动态的调控机制,完善陆地生态系统碳-氮耦合循环模型,有效降低区域陆地碳汇评估的不确定性,并可为陆地生态系统应对全球变化提供科学依据。     

Incorporation of Plant Residues into Soil Organic Matter Fractions With Grassland Management Practices in the North American Midwest

Disturbed grassland soils are often cited as having the potential to store large amounts of carbon (C). Fertilization of grasslands can promote soil C storage, but little is known about the generation of recalcitrant pools of soil organic matter (SOM) with management treatments, which is critical for long-term soil C storage. We used a combination of soil incubations, size fractionation and acid hydrolysis of SOM, [C], [N], and stable isotopic analyses, and biomass quality indices to examine how fertilization and haying can impact SOM dynamics in Kansan grassland soils. Fertilized soils possessed 113% of the C possessed by soils subjected to other treatments, an increase predominantly harbored in the largest size fraction (212–2,000 μm). This fraction is frequently associated with more labile material. Haying and fertilization/haying, treatments that more accurately mimic true management techniques, did not induce any increase in soil C. The difference in ¹⁵N-enrichment between size fractions was consistent with a decoupling of SOM processing between pools with fertilization, congruent with gains of SOM in the largest size fraction promoted by fertilization not moving readily into smaller fractions that frequently harbor more recalcitrant material. Litterfall and root biomass C inputs increased 104% with fertilization over control plots, and this material possessed lower C:N ratios. Models of incubation mineralization kinetics indicate that fertilized soils have larger pools of labile organic C. Model estimates of turnover rates of the labile and recalcitrant C pools did not differ between treatments (65.5 ± 7.2 and 2.9 ± 0.3 μg C d⁻¹, respectively). Although fertilization may promote greater organic inputs into these soils, much of that material is transformed into relatively labile forms of soil C; these data highlight the challenges of managing grasslands for long-term soil C sequestration.     

Rapid soil formation after glacial retreat shaped by spatial patterns of organic matter accrual in microaggregates

Global change contributes to the retreat of glaciers at unprecedented rates. The deglaciation facilitates biogeochemical processes on glacial deposits with initiating soil formation as an important driver of evolving ecosystems. The underlying mechanisms of soil formation and the association of soil organic matter (SOM) with mineral particles remain unclear, although further insights are critical to understand carbon sequestration in soils. We investigated the microspatial arrangement of SOM coatings at intact soil microaggregate structures during various stages of ecosystem development from 15 to >700 years after deglaciation in the proglacial environment of the Damma glacier (Switzerland). The functionally important clay‐sized fraction (<2 μm) was separated into two density fractions with different amounts of organo‐mineral associations: light (1.6–2.2 g/cm³) and heavy (>2.2 g/cm³). To quantify how SOM extends across the surface of mineral particles (coverage) and whether SOM coatings are distributed in fragmented or connected patterns (connectivity), we developed an image analysis protocol based on nanoscale secondary ion mass spectrometry (NanoSIMS). We classified SOM and mineral areas depending on the ¹⁶O^?, ¹²C^?, and ¹²C¹⁴N^? distributions. With increasing time after glacial retreat, the microspatial coverage and connectivity of SOM increased rapidly. The rapid soil formation led to a succession of patchy distributed to more connected SOM coatings on soil microaggregates. The maximum coverage of 55% at >700 years suggests direct evidence for SOM sequestration being decoupled from the mineral surface, as it was not completely masked by SOM and retained its functionality as an ion exchange site. The chemical composition of SOM coatings showed a rapid change toward a higher CN:C ratio already at 75 years after glacial retreat, which was associated with microbial succession patterns reflecting high N assimilation. Our results demonstrate that rapid SOM sequestration drives the microspatial succession of SOM coatings in soils, a process that can stabilize SOM for the long term.     

Plant litter chemistry alters the content and composition of organic carbon associated with soil mineral and aggregate fractions in invaded ecosystems

Through the input of disproportionate quantities of chemically distinct litter, invasive plants may potentially influence the fate of organic matter associated with soil mineral and aggregate fractions in some of the ecosystems they invade. Although context dependent, these native ecosystems subjected to prolonged invasion by exotic plants may be instrumental in distinguishing the role of plant–microbe–mineral interactions from the broader edaphic and climatic influences on the formation of soil organic matter (SOM). We hypothesized that the soils subjected to prolonged invasion by an exotic plant that input recalcitrant litter (Japanese knotweed, Polygonum cuspidatum) would have a greater proportion of plant‐derived carbon (C) in the aggregate fractions, as compared with that in adjacent soil inhabited by native vegetation that input labile litter, whereas the soils under an invader that input labile litter (kudzu, Pueraria lobata) would have a greater proportion of microbial‐derived C in the silt‐clay fraction, as compared with that in adjacent soils that receive recalcitrant litter. At the knotweed site, the higher C content in soils under P. cuspidatum, compared with noninvaded soils inhabited by grasses and forbs, was limited to the macroaggregate fraction, which was abundant in plant biomarkers. The noninvaded soils at this site had a higher abundance of lignins in mineral and microaggregate fractions and suberin in the macroaggregate fraction, partly because of the greater root density of the native species, which might have had an overriding influence on the chemistry of the above‐ground litter input. At the kudzu site, soils under P. lobata had lower C content across all size fractions at a 0–5 cm soil depth despite receiving similar amounts of Pinus litter. Contrary to our prediction, the noninvaded soils receiving recalcitrant Pinus litter had a similar abundance of plant biomarkers across both mineral and aggregate fractions, potentially because of the higher surface area of soil minerals at this site. The plant biomarkers were lower in the aggregate fractions of the P. lobata‐invaded soils, compared with noninvaded pine stands, potentially suggesting a microbial co‐metabolism of pine‐derived compounds. These results highlight the complex interactions among litter chemistry, soil biota, and minerals in mediating soil C storage in unmanaged ecosystems; these interactions are particularly important under global changes that may alter plant species composition and hence the quantity and chemistry of litter inputs in terrestrial ecosystems.     

Carbon storage capacity of semi‐arid grassland soils and sequestration potentials in northern China

Organic carbon (OC) sequestration in degraded semi‐arid environments by improved soil management is assumed to contribute substantially to climate change mitigation. However, information about the soil organic carbon (SOC) sequestration potential in steppe soils and their current saturation status remains unknown. In this study, we estimated the OC storage capacity of semi‐arid grassland soils on the basis of remote, natural steppe fragments in northern China. Based on the maximum OC saturation of silt and clay particles <20 μm, OC sequestration potentials of degraded steppe soils (grazing land, arable land, eroded areas) were estimated. The analysis of natural grassland soils revealed a strong linear regression between the proportion of the fine fraction and its OC content, confirming the importance of silt and clay particles for OC stabilization in steppe soils. This relationship was similar to derived regressions in temperate and tropical soils but on a lower level, probably due to a lower C input and different clay mineralogy. In relation to the estimated OC storage capacity, degraded steppe soils showed a high OC saturation of 78–85% despite massive SOC losses due to unsustainable land use. As a result, the potential of degraded grassland soils to sequester additional OC was generally low. This can be related to a relatively high contribution of labile SOC, which is preferentially lost in the course of soil degradation. Moreover, wind erosion leads to substantial loss of silt and clay particles and consequently results in a direct loss of the ability to stabilize additional OC. Our findings indicate that the SOC loss in semi‐arid environments induced by intensive land use is largely irreversible. Observed SOC increases after improved land management mainly result in an accumulation of labile SOC prone to land use/climate changes and therefore cannot be regarded as contribution to long‐term OC sequestration.     

Mechanisms of C Sequestration in Soils of Latin America

Carbon (C) sequestration, defined as the process whereby atmospheric CO₂ is transferred into a long-lived C pool, is an important issue not only in the scientific community but also in the society at large because of its potential role in off-setting fossil fuel emissions. Through photosynthesis this C is stored in plants and through decomposition, trunks, branches, leaves and roots are incorporated in the soil via the action of different soil organisms, i.e., bacteria, fungi and invertebrates. This, together with the C exudates from roots that are utilized by microbial populations, constitutes the natural pathways of incorporating biomass-C into the soil. The amount of C stored in terrestrial ecosystems is the third largest among the global C pools. Soil organic carbon (SOC) up to 3 m is 2,344 Pg C (1 Petagram = 10¹⁵ g), and the SOC pool in tropical soils is approximately 30% of the global pool. Abiotic factors, which moderate C sequestration in soils are clay content, mineralogy, structural stability, landscape position, and soil moisture and temperature regimes. On the other hand, biotic factors involved in soil C sequestration are determined by the activities of soil organisms. However, models do not include the formation, stabilization and lifespan of the aggregates that have been biologically produced, including roots. This is not only due to the lack of studies on this subject, but also to overlooking the role of soil organisms in soil aggregation. Furthermore, there is a lack of comprehensive knowledge regarding the processes that control dissolved organic carbon (DOC) fluxes in soils and its role in the global budget of C sequestration. The boundaries of ecosystems are not considered in the studies of the subject, as it may be the case for terrestrial C sequestration, since the borders around the sites under study constitute pathways for the flow of C between sites and through the landscape. The concentrations of DOC in deep soil horizons and the contribution to DOC fluxes (exports) are relatively small, from 4 to 37 g DOC m^?2 yr^?1 retained in the mineral subsoil. In South America, although substantial research has been done under different ecosystems and land use systems in some countries, like Brazil, Colombia, Argentina, there is a need to conduct more studies with agreed standard methodologies in natural ecosystems and agricultural systems, and in other areas of Central America few studies have been undertaken to date. The principal objective of this review was to address the main mechanisms that determine SOC and SIC sequestration in soils of Latin America, and include: physical aggregate protection, SOC-clay interaction, DOC transport, bioturbation by soil organisms, and the formation of secondary carbonates. All of these mechanisms are generally explained by physical and chemical processes. In contrast, this review takes a soil ecological approach to describe the mechanisms listed above.     

Influence of rhizodeposition under elevated CO2 on plant nutrition and soil organic matter

Atmospheric CO₂ concentrations can influence ecosystem carbon storage through net primary production (NPP), soil carbon storage, or both. In assessing the potential for carbon storage in terrestrial ecosystems under elevated CO₂, both NPP and processing of soil organic matter (SOM), as well as the multiple links between them, must be examined. Within this context, both the quantity and quality of carbon flux from roots to soil are important, since roots produce specialized compounds that enhance nutrient acquisition (affecting NPP), and since the flux of organic compounds from roots to soil fuels soil microbial activity (affecting processing of SOM).From the perspective of root physiology, a technique is described which uses genetically engineered bacteria to detect the distribution and amount of flux of particular compounds from single roots to non-sterile soils. Other experiments from several labs are noted which explore effects of elevated CO₂ on root acid phosphatase, phosphomonoesterase, and citrate production, all associated with phosphorus nutrition. From a soil perspective, effects of elevated CO₂ on the processing of SOM developed under a C4 grassland but planted with C3 California grassland species were examined under low (unamended) and high (amended with 20 g m^–2 NPK) nutrients; measurements of soil atmosphere 13C combined with soil respiration rates show that during vegetative growth in February, elevated CO₂ decreased respiration of carbon from C4 SOM in high nutrient soils but not in unamended soils.This emphasis on the impacts of carbon loss from roots on both NPP and SOM processing will be essential to understanding terrestrial ecosystem carbon storage under changing atmospheric CO₂ concentrations.Abbreviations SOM soil organic matter - NPP net primary productivity - NEP net ecosystem productivity - PNPP p-nitrophenyl phosphate     

Nitrogen addition alters mineralization dynamics of 13C‐depleted leaf and twig litter and reduces leaching of older DOC from mineral soil

Recent reviews indicate that N deposition increases soil organic matter (SOM) storage in forests but the undelying processes are poorly understood. Our aim was to quantify the impacts of increased N inputs on soil C fluxes such as C mineralization and leaching of dissolved organic carbon (DOC) from different litter materials and native SOM. We added 5.5 g N m^?2 yr^?1 as NH₄NO₃ over 1 year to two beech forest stands on calcareous soils in the Swiss Jura. We replaced the native litter layer with ¹³C‐depleted twigs and leaves (δ¹³C: ?38.4 and ?40.8‰) in late fall and measured N effects on litter‐ and SOM‐derived C fluxes. Nitrogen addition did not significantly affect annual C losses through mineralization, but altered the temporal dynamics in litter mineralization: increased N inputs stimulated initial mineralization during winter (leaves: +25%; twigs: +22%), but suppressed rates in the subsequent summer. The switch from a positive to a negative response occurred earlier and more strongly for leaves than for twigs (?21% vs. 0%). Nitrogen addition did not influence microbial respiration from the nonlabeled calcareous mineral soil below the litter which contrasts with recent meta‐analysis primarily based on acidic soils. Leaching of DOC from the litter layer was not affected by NH₄NO₃ additions, but DOC fluxes from the mineral soils at 5 and 10 cm depth were significantly reduced by 17%. The ¹³C tracking indicated that litter‐derived C contributed less than 15% of the DOC flux from the mineral soil, with N additions not affecting this fraction. Hence, the suppressed DOC fluxes from the mineral soil at higher N inputs can be attributed to reduced mobilization of nonlitter derived ‘older’ DOC. We relate this decline to an altered solute chemistry by NH₄NO₃ additions, an increased ionic strength and acidification resulting from nitrification, rather than to a change in microbial decomposition.     

Interactions between Carbon and Nitrogen Mineralization and Soil Organic Matter Chemistry in Arctic Tundra Soils

We used long-term laboratory incubations and chemical fractionation to characterize the mineralization dynamics of organic soils from tussock, shrub, and wet meadow tundra communities, to determine the relationship between soil organic matter (SOM) decomposition and chemistry, and to quantify the relative proportions of carbon (C) and nitrogen (N) in tundra SOM that are biologically available for decomposition. In all soils but shrub, we found little decline in respiration rates over 1 year, although soils respired approximately a tenth to a third of total soil C. The lack of decline in respiration rates despite large C losses indicates that the quantity of organic matter available was not controlling respiration and thus suggests that something else was limiting microbial activity. To determine the nature of the respired C, we analyzed soil chemistry before and after the incubation using a peat fractionation scheme. Despite the large losses of soil C, SOM chemistry was relatively unchanged after the incubation. The decomposition dynamics we observed suggest that tundra SOM, which is largely plant detritus, fits within existing concepts of the litter decay continuum. The lack of changes in organic matter chemistry indicates that this material had already decomposed to the point where the breakdown of labile constituents was tied to lignin decomposition. N mineralization was correlated with C mineralization in our study, but shrub soil mineralized more and tussock soil less N than would have been predicted by this correlation. Our results suggest that a large proportion of tundra SOM is potentially mineralizable, despite the fact that decomposition was dependent on lignin breakdown, and that the historical accumulation of organic matter in tundra soils is the result of field conditions unfavorable to decomposition and not the result of fundamental chemical limitations to decomposition. Our study also suggests that the anticipated increases in shrub dominance may substantially alter the dynamics of SOM decomposition in the tundra. Received 31 January 2002; accepted 16 July 2002.     

Anthropogenic N deposition increases soil organic matter accumulation without altering its biochemical composition

Accumulating evidence indicates that future rates of atmospheric N deposition have the potential to increase soil C storage by reducing the decay of plant litter and soil organic matter (SOM). Although the microbial mechanism underlying this response is not well understood, a decline in decay could alter the amount, as well as biochemical composition of SOM. Here, we used size‐density fractionation and solid‐state ¹³C‐NMR spectroscopy to explore the extent to which declines in microbial decay in a long‐term (ca. 20 yrs.) N deposition experiment have altered the biochemical composition of forest floor, bulk mineral soil, as well as free and occluded particulate organic matter. Significant amounts of organic matter have accumulated in occluded particulate organic matter (~20%; oPOM); however, experimental N deposition had not altered the abundance of carboxyl, aryl, alkyl, or O/N‐alkyl C in forest floor, bulk mineral soil, or any soil fraction. These observations suggest that biochemically equivalent organic matter has accumulated in oPOM at a greater rate under experimental N deposition, relative to the ambient treatment. Although we do not understand the process by which experimental N deposition has fostered the occlusion of organic matter by mineral soil particles, our results highlight the importance of interactions among the products of microbial decay and the chemical and physical properties of silt and clay particles that occlude organic matter from microbial attack. Because oPOM can reside in soils for decades to centuries, organic matter accumulating under future rates of anthropogenic N deposition could remain in soil for long periods of time. If temperate forest soils in the Northern Hemisphere respond like those in our experiment, then unabated deposition of anthropogenic N from the atmosphere has the potential to foster greater soil C storage, especially in fine‐texture forest soils.     

草地土壤固碳潜力研究进展

土壤固碳功能和固碳潜力已成为全球气候变化和陆地生态系统研究的重点。草地土壤有机碳库,作为陆地土壤有机碳库的重要组成部分,其较小幅度的波动,将会影响整个陆地生态系统碳循环,进而影响全球气候变化。因此,深入研究草地土壤固碳功能和固碳潜力对于适应和减缓气候变化具有重要意义。在土壤固碳潜力相关概念界定基础上,结合《2006年IPCC国家温室气体清单指南》,从样点及区域尺度上综述了目前关于草地土壤固碳潜力的一般估算方法,同时对各类方法的特点及适用性进行了评述,提出了草地生态系统固碳潜力研究概念模型。最后在对草地土壤固碳的影响因素及固碳措施总结的基础上,阐明了草地土壤有机碳固定研究中存在的问题和发展前景。     

Assessing the impact of land-use change on soil C sequestration in agricultural soils by means of organic matter fractionation and stable C isotopes

Within the framework of the Kyoto Protocol, the potential mitigation of greenhouse gas emissions by terrestrial ecosystems has placed focus on carbon sequestration following afforestation of former arable land. Central to this soil C sequestration are the dynamics of soil organic matter (SOM). In North Eastern Italy, a mixed deciduous forest was planted on continuous maize field soil with a strong C₄ isotopic C signature 20 years ago. In addition, a continuous maize field and a relic of the original permanent grassland were maintained at the site, thus offering the opportunity to compare the impacts on soil C dynamics by conventional agriculture, afforestation and permanent grassland. Soil samples from the afforested, grassland and agricultured systems were separated in three aggregate size classes, and inter‐ vs. intra‐aggregate particulate organic matter was isolated. All fractions were analyzed for their C content and isotopic signature. The distinct ¹³C signature of the C derived from maize vegetation allowed the calculation of proportions of old vs. forest‐derived C of the physically defined fractions of the afforested soil. Long‐term agricultural use significantly decreased soil C content (?48%), in the top 10 cm, but not SOM aggregation, as compared to permanent grassland. After 20 years, afforestation increased the total amount of soil C by 23% and 6% in the 0–10 and in the 10–30 cm depth layer, respectively. Forest‐derived carbon contributed 43% and 31% to the total soil C storage in the afforested systems in the 0–10 and 10–30 cm depths, respectively. Furthermore, afforestation resulted in significant sequestration of new C and stabilization of old C in physically protected SOM fractions, associated with microaggregates (53–250 μm) and silt&clay (<53 μm).     

气候变化对陆地生态系统土壤有机碳储量变化的影响

通过研究气候变化对土壤有机碳储藏的影响,对预测未来气候变化下土壤有机碳动态变化与深入理解陆地生态系统变化和气候变化之间的相互作用有着极其重要的意义。本文归纳了土壤类型法、模型模拟法等途径对土壤有机碳储量估算的结果并分析它们各自的不确定性,综述了气候变化对土壤碳贮藏影响机理的研究与相应过程模拟的模型研究进展,并综合分析了当前研究中还存在的问题与不足。     

Soil organic matter turnover is governed by accessibility not recalcitrance

Mechanisms to mitigate global climate change by sequestering carbon (C) in different ‘sinks' have been proposed as at least temporary measures. Of the major global C pools, terrestrial ecosystems hold the potential to capture and store substantially increased volumes of C in soil organic matter (SOM) through changes in management that are also of benefit to the multitude of ecosystem services that soils provide. This potential can only be realized by determining the amount of SOM stored in soils now, with subsequent quantification of how this is affected by management strategies intended to increase SOM concentrations, and used in soil C models for the prediction of the roles of soils in future climate change. An apparently obvious method to increase C stocks in soils is to augment the soil C pools with the longest mean residence times (MRT). Computer simulation models of soil C dynamics, e.g. RothC and Century, partition these refractory constituents into slow and passive pools with MRTs of centuries to millennia. This partitioning is assumed to reflect: (i) the average biomolecular properties of SOM in the pools with reference to their source in plant litter, (ii) the accessibility of the SOM to decomposer organisms or catalytic enzymes, or (iii) constraints imposed on decomposition by environmental conditions, including soil moisture and temperature. However, contemporary analytical approaches suggest that the chemical composition of these pools is not necessarily predictable because, despite considerable progress with understanding decomposition processes and the role of decomposer organisms, along with refinements in simulation models, little progress has been made in reconciling biochemical properties with the kinetically defined pools. In this review, we will explore how advances in quantitative analytical techniques have redefined the new understanding of SOM dynamics and how this is affecting the development and application of new modelling approaches to soil C.     

Aggregate formation and organo-mineral association affect characteristics of soil organic matter across soil horizons and parent materials in temperate broadleaf forest

Precise assessment of soil organic carbon (OC) storage requires understanding of soil type and depth specific differences in organic matter (OM) stabilization. Therefore, we aimed to analyze OC dynamics down the soil profile and to clarify the effect of depth on the importance of aggregate formation and mineral adsorption for OC storage in mature beech forest soils developed from different parent materials. Aggregate size and density fractions were separated from samples of top and subsoil horizons, which were quantified and analyzed by infrared spectroscopy. We also determined the microbial biomass C (C_mic) and the amount of C decomposed within incubation experiments (CO₂-C) for the bulk soil samples. OC stabilized via aggregate formation and mineral association significantly increased with soil depth. However, this stabilized pool seemed to fuel the labile OM stronger in the subsoil than in the topsoil because the CO₂-C/SOC and CO₂-C/C_mic ratios increased with depth. Measured differences in the magnitude of the detected stabilization and destabilization patterns were attributed to parent material and soil horizon, indicating pronounced spatial and vertical heterogeneity in the contribution of soils under temperate broadleaf forest to terrestrial C sequestration. Considering such site and depth specific differences will improve assessment and modelling of soil OC storage for areas covered with the same forest type but with high pedogenetic diversity.

     

Treeline shifts in the Ural mountains affect soil organic matter dynamics

Historical photographs document that during the last century, forests have expanded upwards by 60–80 m into former tundra of the pristine Ural mountains. We assessed how the shift of the high‐altitude treeline ecotone might affect soil organic matter (SOM) dynamics. On the gentle slopes of Mali Iremel in the Southern Urals, we (1) determined the differences in SOM stocks and properties from the tundra at 1360 m above sea level (a.s.l.) to the subalpine forest at 1260 m a.s.l., and (2) measured carbon (C) and nitrogen (N) mineralization from tundra and forest soils at 7 and 20 °C in a 6‐month incubation experiment. C stocks of organic layers were 3.6±0.3 kg C m^?2 in the tundra and 1.9±0.2 kg C m^?2 in the forest. Mineral soils down to the bedrock stored significantly more C in the forest, and thus, total soil C stocks were slightly but insignificantly greater in the forest (+3 kg C m^?2). Assuming a space for time approach based on tree ages suggests that the soil C sink due to the forest expansion during the last century was at most 30 g C m^?2 yr^?1. Diffuse reflective infrared spectroscopy and scanning calorimetry revealed that SOM under forest was less humified in both organic and mineral horizons and, therefore, contained more available substrate. Consistent with this result, C mineralization rates of organic layers and A horizons of the forest were two to four times greater than those of tundra soils. This difference was similar in magnitude to the effect of increasing the incubation temperature from 7 to 20 °C. Hence, indirect climate change effects through an upward expansion of forests can be much larger than direct warming effects (Δ0.3 K across the treeline). Net N mineralization was 2.5 to six times greater in forest than in tundra soils, suggesting that an advancing treeline likely increases N availability. This may provide a nutritional basis for the fivefold increase in plant biomass and a tripling in productivity from the tundra to the forest. In summary, our results suggest that an upward expansion of forest has small net effects on C storage in soils but leads to changes in SOM quality, accelerates C cycling and increases net N mineralization, which in turn might stimulate plant growth and thus C sequestration in tree biomass.     

Biochar stability in soil: meta‐analysis of decomposition and priming effects

The stability and decomposition of biochar are fundamental to understand its persistence in soil, its contribution to carbon (C) sequestration, and thus its role in the global C cycle. Our current knowledge about the degradability of biochar, however, is limited. Using 128 observations of biochar‐derived CO₂ from 24 studies with stable (¹³C) and radioactive (¹⁴C) carbon isotopes, we meta‐analyzed the biochar decomposition in soil and estimated its mean residence time (MRT). The decomposed amount of biochar increased logarithmically with experimental duration, and the decomposition rate decreased with time. The biochar decomposition rate varied significantly with experimental duration, feedstock, pyrolysis temperature, and soil clay content. The MRTs of labile and recalcitrant biochar C pools were estimated to be about 108 days and 556 years with pool sizes of 3% and 97%, respectively. These results show that only a small part of biochar is bioavailable and that the remaining 97% contribute directly to long‐term C sequestration in soil. The second database (116 observations from 21 studies) was used to evaluate the priming effects after biochar addition. Biochar slightly retarded the mineralization of soil organic matter (SOM; overall mean: ?3.8%, 95% CI = ?8.1–0.8%) compared to the soil without biochar addition. Significant negative priming was common for studies with a duration shorter than half a year (?8.6%), crop‐derived biochar (?20.3%), fast pyrolysis (?18.9%), the lowest pyrolysis temperature (?18.5%), and small application amounts (?11.9%). In contrast, biochar addition to sandy soils strongly stimulated SOM mineralization by 20.8%. This indicates that biochar stimulates microbial activities especially in soils with low fertility. Furthermore, abiotic and biotic processes, as well as the characteristics of biochar and soils, affecting biochar decomposition are discussed. We conclude that biochar can persist in soils on a centennial scale and that it has a positive effect on SOM dynamics and thus on C sequestration.     

氮沉降对杉木和枫香土壤氮磷转化及碳矿化的影响

氮沉降是全球变化的重大环境问题,根际是地下生态过程研究的前沿,但目前氮沉降对亚热带地区不同树种土壤氮、磷供应和碳矿化根际过程的影响及其机制尚不清楚。选取典型红壤区15a针叶树杉木(Cunninghamia lanceolata)和阔叶树枫香(Liquidamba formosana)为对象,野外原位开展10 g N m~(-2)a~(-1)氮沉降试验3a,于2014年8月收集杉木和枫香根际土壤和非根际土壤,测定其p H值、有效氮、速效磷、水溶性有机碳及其34 d有机碳矿化动态,并计算根际效应。结果表明:氮沉降显著降低两个树种土壤p H值和杉木根际土壤速效磷(P0.05);提高枫香非根际土壤NO~-_3-N和杉木非根际土壤水溶性有机碳含量。同时,氮沉降显著提高杉木土壤有机碳矿化速率,根际和非根际的增幅分别为71.2%和41.2%,降低枫香土壤有机碳矿化速率,根际和非根际的降幅分别为10.6%和44.1%。此外,氮沉降显著降低枫香土壤NO~-_3-N和有机碳前期矿化速率的根际效应,增强后期矿化速率的根际效应,而杉木对氮沉降响应不显著。可见,氮沉降可显著改变树木土壤养分供应和有机碳稳定性,且丘陵红壤区针叶树和阔叶树根际过程对氮沉降的响应模式有别。率先报道了亚热带不同树种根际碳、氮、磷耦合过程对氮沉降的响应格局,并较好地揭示了针叶树和阔叶树对氮沉降响应的分异机制。     

Soil carbon sequestration in a pine forest after 9 years of atmospheric CO2 enrichment

The impact of anthropogenic CO₂ emissions on climate change may be mitigated in part by C sequestration in terrestrial ecosystems as rising atmospheric CO₂ concentrations stimulate primary productivity and ecosystem C storage. Carbon will be sequestered in forest soils if organic matter inputs to soil profiles increase without a matching increase in decomposition or leaching losses from the soil profile, or if the rate of decomposition decreases because of increased production of resistant humic substances or greater physical protection of organic matter in soil aggregates. To examine the response of a forest ecosystem to elevated atmospheric CO₂ concentrations, the Duke Forest Free‐Air CO₂ Enrichment (FACE) experiment in North Carolina, USA, has maintained atmospheric CO₂ concentrations 200 μL L^?1 above ambient in an aggrading loblolly pine (Pinus taeda) plantation over a 9‐year period (1996–2005). During the first 6 years of the experiment, forest‐floor C and N pools increased linearly under both elevated and ambient CO₂ conditions, with significantly greater accumulations under the elevated CO₂ treatment. Between the sixth and ninth year, forest‐floor organic matter accumulation stabilized and C and N pools appeared to reach their respective steady states. An additional C sink of ～30 g C m^?2 yr^?1 was sequestered in the forest floor of the elevated CO₂ treatment plots relative to the control plots maintained at ambient CO₂ owing to increased litterfall and root turnover during the first 9 years of the study. Because we did not detect any significant elevated CO₂ effects on the rate of decomposition or on the chemical composition of forest‐floor organic matter, this additional C sink was likely related to enhanced litterfall C inputs. We also failed to detect any statistically significant treatment effects on the C and N pools of surface and deep mineral soil horizons. However, a significant widening of the C : N ratio of soil organic matter (SOM) in the upper mineral soil under both elevated and ambient CO₂ suggests that N is being transferred from soil to plants in this aggrading forest. A significant treatment × time interaction indicates that N is being transferred at a higher rate under elevated CO₂ (P=0.037), suggesting that enhanced rates of SOM decomposition are increasing mineralization and uptake to provide the extra N required to support the observed increase in primary productivity under elevated CO₂.