Alternative explanations for rising dissolved organic carbon export from organic soils

Since 1988, there has been, on average, a 91% increase in dissolved organic carbon (DOC) concentrations of UK lakes and streams in the Acid Waters Monitoring Network (AWMN). Similar DOC increases have been observed in surface waters across much of Europe and North America. Much of the debate about the causes of rising DOC has, as in other studies relating to the carbon cycle, focused on factors related to climate change. Data from our peat‐core experiments support an influence of climate on DOC, notably an increase in production with temperature under aerobic, and to a lesser extent anaerobic, conditions. However, we argue that climatic factors may not be the dominant drivers of DOC change. DOC solubility is suppressed by high soil water acidity and ionic strength, both of which have decreased as a result of declining sulphur deposition since the 1980s, augmented during the 1990s in the United Kingdom by a cyclical decline in sea‐salt deposition. Our observational and experimental data demonstrate a clear, inverse and quantitatively important link between DOC and sulphate concentrations in soil solution. Statistical analysis of 11 AWMN lakes suggests that rising temperature, declining sulphur deposition and changing sea‐salt loading can account for the majority of the observed DOC trend. This combination of evidence points to the changing chemical composition of atmospheric deposition, particularly the substantial reduction in anthropogenic sulphur emissions during the last 20 years, as a key cause of rising DOC. The implications of rising DOC export for the carbon cycle will be very different if linked primarily to decreasing acid deposition, rather than to changes in climate, suggesting that these systems may be recovering rather than destabilising.     

Does elevated nitrogen deposition or ecosystem recovery from acidification drive increased dissolved organic carbon loss from upland soil? A review of evidence from field nitrogen addition experiments

Dissolved organic carbon (DOC) concentrations have risen in upland waters across large areas of Europe and North America. Two proposed drivers of these increases are (1) deposition of atmospheric pollutant nitrogen (N) with consequent effects on plant and decomposer carbon dynamics, and (2) soil recovery from acidification associated with decreasing sulphur deposition. Examination of 12 European and North American field N addition experiments showed inconsistent (positive, neutral, and negative) responses of DOC to N addition. However, responses were linked to the form of N added and to resulting changes in soil acidity. Sodium nitrate additions consistently increased DOC, whereas ammonium salts additions usually decreased DOC. Leachate chemistry was used to calculate an index of “ANC forcing” of the effect of fertilization on the acid-base balance, which showed that DOC increased in response to all de-acidifying N additions, and decreased in response to all but three acidifying N additions. Exceptions occurred at two sites where N additions caused tree mortality, and one experiment located on an older, unglaciated soil with high anion adsorption capacity. We conclude that collectively these experiments do not provide clear support for the role of N deposition as the sole driver of rising DOC, but are largely consistent with an acidity-change mechanism. It is however possible that the unintended effect of acidity change on DOC mobility masks genuine effects of experimental N enrichment on DOC production and degradation. We suggest that there is a need, more generally, for interpretation of N manipulation experiments to take account of the effects that experimentally-induced changes in acidity, rather than elevated N per se, may have on ecosystem biogeochemistry.     

Fine-scale temporal characterization of trends in soil water dissolved organic carbon and potential drivers

Long-term monitoring of surface water quality has shown increasing concentrations of dissolved organic carbon (DOC) across a large part of the Northern Hemisphere. Several drivers have been implicated including climate change, land management change, nitrogen and sulphur deposition and CO₂ enrichment. Analysis of stream water data, supported by evidence from laboratory studies, indicates that an effect of declining sulphur deposition on catchment soil chemistry is likely to be the primary mechanism, but there are relatively few long term soil water chemistry records in the UK with which to investigate this, and other, hypotheses directly. In this paper, we assess temporal relationships between soil solution chemistry and parameters that have been argued to regulate DOC production and, using a unique set of co-located measurements of weather and bulk deposition and soil solution chemistry provided by the UK Environmental Change Network and the Intensive Forest Monitoring Level II Network. We used statistical non-linear trend analysis to investigate these relationships at 5 forested and 4 non-forested sites from 1993 to 2011. Most trends in soil solution DOC concentration were found to be non-linear. Significant increases in DOC occurred mostly prior to 2005. The magnitude and sign of the trends was associated qualitatively with changes in acid deposition, the presence/absence of a forest canopy, soil depth and soil properties. The strongest increases in DOC were seen in acidic forest soils and were most clearly linked to declining anthropogenic acid deposition, while DOC trends at some sites with westerly locations appeared to have been influenced by shorter-term hydrological variation. The results indicate that widespread DOC increases in surface waters observed elsewhere, are most likely dominated by enhanced mobilization of DOC in surficial organic horizons, rather than changes in the soil water chemistry of deeper horizons. While trends in DOC concentrations in surface horizons have flattened out in recent years, further increases may be expected as soil chemistry continues to adjust to declining inputs of acidity.     

Losses of soil organic carbon under wind erosion in China

Soil organic carbon (SOC) storage generally represents the long‐term net balance of photosynthesis and total respiration in terrestrial ecosystems. However, soil erosion can affect SOC content by direct removal of soil and reduction of the surface soil depth; it also affects plant growth and soil biological activity, soil air CO₂ concentration, water regimes, soil temperature, soil respiration, carbon flux to the atmosphere, and carbon deposition in soil. In arid and semi‐arid region of northern China, wind erosion caused soil degradation and desert expansion. This paper estimated the SOC loss of the surface horizon at eroded regions based on soil property and wind erosion intensity data. The SOC loss in China because of wind erosion was about 75 Tg C yr^?1 in 1990s. The spatial pattern of SOC loss indicates that SOC loss of the surface horizon increases significantly with the increase of soil wind erosion intensity. The comparison of SOC loss and annual net primary productivity (NPP) of terrestrial ecosystem was discussed in wind erosion regions of China. We found that NPP is also low in the eroded regions and heavy SOC loss often occurs in regions where NPP is very small. However, there is potential to improve our study to resolve uncertainty on the soil organic matter oxidation and soil deposition processes in eroded and deposited sites.     

土壤溶解性有机碳在陆地生态系统碳循环中的作用

土壤溶解性有机碳(DOC)是有机碳库的活跃组分,在陆地生态系统碳循环中发挥重要作用.本文从碳循环重要性着手,综述了土壤DOC在土壤碳固持与温室气体排放中的作用;结合我国的现实情况(如土壤酸化、气候变暖等),探讨了土壤DOC的相关影响因素如土壤性质、环境因素、人为活动对土壤DOC的影响及作用机制,对进一步理解土壤DOC在陆地生态系统碳循环与温室气体减排中的作用具有重要意义.     

Soil organic matter and litter chemistry response to experimental N deposition in northern temperate deciduous forest ecosystems

The effects of atmospheric nitrogen (N) deposition on organic matter decomposition vary with the biochemical characteristics of plant litter. At the ecosystem‐scale, net effects are difficult to predict because various soil organic matter (SOM) fractions may respond differentially. We investigated the relationship between SOM chemistry and microbial activity in three northern deciduous forest ecosystems that have been subjected to experimental N addition for 2 years. Extractable dissolved organic carbon (DOC), DOC aromaticity, C : N ratio, and functional group distribution, measured by Fourier transform infrared spectra (FTIR), were analyzed for litter and SOM. The largest biochemical changes were found in the sugar maple–basswood (SMBW) and black oak–white oak (BOWO) ecosystems. SMBW litter from the N addition treatment had less aromaticity, higher C : N ratios, and lower saturated carbon, lower carbonyl carbon, and higher carboxylates than controls; BOWO litter showed opposite trends, except for carbonyl and carboxylate contents. Litter from the sugar maple–red oak (SMRO) ecosystem had a lower C : N ratio, but no change in DOC aromaticity. For SOM, the C : N ratio increased with N addition in SMBW and SMRO ecosystems, but decreased in BOWO; N addition did not affect the aromaticity of DOC extracted from mineral soil. All ecosystems showed increases in extractable DOC from both litter and soil in response to N treatment. The biochemical changes are consistent with the divergent microbial responses observed in these systems. Extracellular oxidative enzyme activity has declined in the BOWO and SMRO ecosystems while activity in the SMBW ecosystem, particularly in the litter horizon, has increased. In all systems, enzyme activities associated with the hydrolysis and oxidation of polysaccharides have increased. At the ecosystem scale, the biochemical characteristics of the dominant litter appear to modulate the effects of N deposition on organic matter dynamics.     

Dissolved organic carbon and its utilization in a riverine wetland ecosystem

Variations in dissolved organic carbon (DOC) concentrations of surface waters and subsurface interstitial groundwater of riparian and wetland soils to 1.2 m depth were evaluated in a riverine wetland ecosystem over one year. DOC was monitored at seven sites within the wetland pond, two sites on the inflow stream, and one site on the outflow stream. Surface concentrations in the inflow stream ranged from 0.74 to 11.6 mg C L^–1 and those of the outflow from 2.1 to 8.0 mg C L^–1 Average DOC from stream floodplain hydrosoils (3.1 to 32.1 mg C L^–1 was greater than DOC from the sediments below the stream channel (1.6 to 6.8 mg C L^–1 Surface DOC within the wetland varied seasonally, with greatest fluctuations in concentrations through the summer and autumn (range 4.8 to 32.6 mg C L^–1 ) during intensive macrophyte growth and bacterial production. DOC was less variable during the winter months (1.7 to 3.3 mg C L^–1 Within the wetland pond, average DOC concentrations (7.1 to 48.2 mg C L^–1) in the subsurface waters were significantly greater (p < 0.05) than average surface concentrations. The microbial availability of surface and subsurface DOC to bacteria was evaluated from losses of DOC by wetland bacteria grown on the DOC. Bacterial growth efficiencies ranged from 5 to 20% and were negatively correlated to the percentage of DOC removed by bacteria (r²=0.93). Throughout the ecosystem, DOC concentrations were greatest in the subsurface waters, but at most depths this DOC was a less suitable substrate than surface DOC for utilization by bacteria.     

Potential for long‐term transfer of dissolved organic carbon from riparian zones to streams in boreal catchments

Boreal regions store most of the global terrestrial carbon, which can be transferred as dissolved organic carbon (DOC) to inland waters with implications for both aquatic ecology and carbon budgets. Headwater riparian zones (RZ) are important sources of DOC, and often just a narrow ‘dominant source layer’ (DSL) within the riparian profile is responsible for most of the DOC export. Two important questions arise: how long boreal RZ could sustain lateral DOC fluxes as the sole source of exported carbon and how its hydromorphological variability influences this role. We estimate theoretical turnover times by comparing carbon pools and lateral exports in the DSL of 13 riparian profiles distributed over a 69 km² catchment in northern Sweden. The thickness of the DSL was 36 ± 18 (average ± SD) cm. Thus, only about one‐third of the 1‐m‐deep riparian profile contributed 90% of the lateral DOC flux. The 13 RZ exported 8.7 ± 6.5 g C m^?2 year^?1, covering the whole range of boreal stream DOC exports. The variation could be explained by local hydromorphological characteristics including RZ width (R² = 0.90). The estimated theoretical turnover times were hundreds to a few thousands of years, that is there is a potential long‐lasting supply of DOC. Estimates of net ecosystem production in the RZ suggest that lateral fluxes, including both organic and inorganic C, could be maintained without drawing down the riparian pools. This was supported by measurements of stream DO¹⁴C that indicated modern carbon as the predominant fraction exported, including streams disturbed by ditching. The transfer of DOC into boreal inland waters from new and old carbon sources has a major influence on surface water quality and global carbon balances. This study highlights the importance of local variations in RZ hydromorphology and DSL extent for future DOC fluxes under a changing climate.     

Modelling the effects of climate change on an acidic upland stream

Most modelling studies of soil and surface water recovery from acidification assume a constant influence of climate over the simulation period. Given the likelihood of future climate change, and recent identification of links between climatic fluctuations and surface water trends on decadal time scales, an attempt is made to simulate a number of climate-related effects on the recovery of an acidified stream in mid-Wales. Empirical relationships were derived to model past and future variations in (i) runoff, as a function of rainfall and temperature; (ii) stream chloride concentration and sea-salt deposition, as a function of the North Atlantic Oscillation Index (NAOI); and (iii) stream dissolved organic carbon (DOC) concentration, as a function of summer temperatures and sulphur deposition. Incorporating these relationships in the MAGIC dynamic model reproduced a significant part of the observed variation in streamwater chemistry. Current scenarios of rising UK temperature and NAOI, and falling rainfall and acid deposition, were used to forecast effects of climate change on soil and water recovery from acidification. Results suggest that increasing DOC would have a significant negative impact on soil recovery, with elevated organic acidity lowering soil water pH and severely depleting soil base saturation. The resulting increase in soil base cation export would, however, have a positive impact on streamwater recovery. For increased sea-salt deposition, effects are essentially the opposite; increased base cation inputs enhance the recovery of soil base saturation, but displace acidity to the stream. However, simulated effects of raising DOC considerably outweighed those of increased sea-salt deposition. It is argued that greater consideration of these, and other, climatic effects on biogeochemical cycles needs to be taken when predicting the recovery of soils and surface waters from acidification.     

Concentration and Fluxes of Dissolved Organic Carbon (DOC) in Three Norway Spruce Stands along a Climatic Gradient in Sweden

Leaching of dissolved organic carbon (DOC) from the forest floor and transport in soil solution into the mineral soil are important for carbon cycling in boreal forest ecosystems. We examined DOC concentrations in bulk deposition, throughfall and in soil solutions collected under the O and B horizons in three Norway spruce stands along a climatic gradient in Sweden. Mean annual temperature for the three sites was 5.5, 3.4 and 1.2 °C. At each site we also examined the effect of soil moisture on DOC dynamics along a moisture gradient (dry, mesic and moist plots). To obtain information about the fate of DOC leached from the O horizon into the mineral soil, ¹⁴C measurements were made on bulk organic matter and DOC. The concentration and fluxes of DOC in O horizon leachates were highest at the southern site and lowest at the northern. Average DOC concentrations at the southern, central and northern sites were 49, 39 and 30 mg l⁻¹, respectively. We suggest that DOC leaching rates from O horizons were related to the net primary production of the ecosystem. Soil temperature probably governed the within-year variation in DOC concentration in O horizon leachates, but the peak in DOC was delayed relative to that of temperature, probably due to sorption processes. Neither soil moisture regime (dry, mesic or moist plots) nor seasonal variation in soil moisture seemed to be of any significance for the concentration of DOC leached from the O horizon. The ¹⁴C measurements showed that DOC in soil solution collected below the B horizon was derived mainly from the B horizon itself, rather than from the O horizon, indicating a substantial exchange (sorption–desorption reactions) between incoming DOC and soil organic carbon in the mineral soil.     

火烧对森林土壤有机碳的影响研究进展

对国内外火烧影响森林土壤有机碳动态的研究成果进行了综合述评。较多研究表明低强度火烧不会造成土壤有机碳贮量的明显变化,但火烧非常强烈而彻底,土壤有机碳明显减少。有限研究表明火烧对森林土壤呼吸的影响结果有增加、降低或无影响,因火烧强度、火后观测时间、森林类型、火烧迹地上植被恢复进程和气候条件等而异。同时,火烧对土壤有机碳组分(活性有机碳和黑碳)也具有不同程度的影响。随着全球变化研究的深入,火烧作为森林主要管理措施对大气CO2浓度影响亦愈来愈受重视,今后应着重开展以下几方面研究:(1)扩大气候和经营管理的变化对森林土壤有机碳贮量时空动态影响研究;(2)深入探讨火烧影响土壤CO2释放的过程及机理;(3)加强火烧历史和频率对黑碳影响的研究;(4)从广度和深度上加强火烧等经营措施对亚热带森林土壤碳动态影响的研究。     

森林生态系统可溶性碳和颗粒碳通量

可溶性碳(Dissolved carbon,DC)和颗粒碳(particulate carbon,PC)通量作为森林生态系统碳收支的重要组分,在森林固碳功能的评价和模型预测中具有重要意义,但常因认识不足、测定困难等而在森林碳汇研究中被忽略。综述了森林生态系统DC和PC的组成、作用、相关生态过程及其影响因子,并展望了该领域应该优先考虑的研究问题。森林生态系统DC和PC主要包括可溶性有机碳、可溶性无机碳和颗粒有机碳,主要来源于生态系统的净初级生产量。DC和PC是森林土壤的活性碳库,主要以大气沉降、穿透雨和凋落物的形式输入森林土壤系统,并通过土壤呼吸、侧向运输及渗透流失的方式输出生态系统。从局域尺度看,DC和PC通量受根系分泌、细根分解、微生物周转等生物过程的影响较大;从区域尺度看,它们受土壤和植被特性、生态过程耦联关系、气候因子以及全球变化的综合影响。该领域应该优先考虑:(1)探索不同时空尺度下森林生态系统DC和PC通量的控制因子及其耦联关系,揭示其中的驱动机理;(2)探索DC和PC与其它森林生态系统碳组分的相互关系及转化,阐明DC和PC通量与其它养分之间潜在的生态化学计量关系;(3)探索全球变化,特别是人类活动(如森林经营)和极端干扰事件(如林火、旱涝、冰冻、冻融交替等)对森林生态系统DC和PC通量的影响。     

Silicate weathering in temperate forest soils: insights from a field experiment

Few studies of silicate mineral weathering have been conducted in carbonate-bearing temperate forest soils. With climate and vegetation held constant, we compared soil mineralogy and major element chemistry of soil waters from a carbonate-free temperate aspen forest site in the Cheboygan watershed, northern Michigan, with that from carbonate-containing soils from experimental tree-growth chambers (low- vs. high- fertility). All soils were well-drained sands (quartz, Na-rich plagioclase, and K-feldspar) with minor amounts of carbonate present only in the experimentally manipulated soils. The Na⁺ concentrations in soil waters corrected for atmospheric deposition (Na*) were used to compare relative rates of plagioclase feldspar weathering across sites. In natural soil water profiles, maximum concentrations of Na*, Si, and dissolved organic carbon (DOC) were observed by a depth of 15 cm, a soil zone free of carbonate minerals. Mean Na* and DOC concentrations were different in the three soils, and increased in the order natural soil < low-fertility chambers < high-fertility chambers. While low pH environments are generally viewed as enhancing weathering rates, here higher Na* appears to be related to high DOC, which is consistent with observed increases in active organic functional groups as pH increases. Our results suggest that under a specific vegetative cover, the soil carbon environment affects the weathering flux observed. Our study also suggests that disturbed soils provide an enhanced physical and chemical environment for weathering. Generalized silicate weathering models may benefit from including the enhancing effects of organic anions at moderate pH in addition to precipitation and temperature.     

Evidence that Soil Carbon Pool Determines Susceptibility of Semi-Natural Ecosystems to Elevated Nitrogen Leaching

Deposition of reactive nitrogen (N) compounds has the potential to cause severe damage to sensitive soils and waters, but the process of ‘nitrogen saturation’ is difficult to demonstrate or predict. This study compares outputs from a simple carbon–nitrogen model with observations of (1) regional- and catchment-scale relationships between surface water nitrate and dissolved organic carbon (DOC), as an indicator of catchment carbon (C) pool; (2) inter-regional variations in soil C/N ratios; and (3) plot scale soil and leachate response to long-term N additions, for a range of UK moorlands. Results suggest that the simple model applied can effectively reproduce observed patterns, and that organic soil C stores provide a critical control on catchment susceptibility to enhanced N leaching, leading to high spatial variability in the extent and severity of current damage within regions of relatively uniform deposition. Results also support the hypothesis that the N richness of organic soils, expressed as C/N ratio, provides an effective indicator of soil susceptibility to enhanced N leaching. The extent to which current C/N is influenced by N deposition, as opposed to factors such as climate and vegetation type, cannot be unequivocally determined on the basis of spatial data. However, N addition experiments at moorland sites have shown a reduction in organic soil C/N. A full understanding of the mechanisms of N-enrichment of soils and waters is essential to the assessment of current sensitivity to, and prediction of future damage from, globally increasing reactive nitrogen deposition.     

Experimental whole‐lake increase of dissolved organic carbon concentration produces unexpected increase in crustacean zooplankton density

The observed pattern of lake browning, or increased terrestrial dissolved organic carbon (DOC) concentration, across the northern hemisphere has amplified the importance of understanding how consumer productivity varies with DOC concentration. Results from comparative studies suggest these increased DOC concentrations may reduce crustacean zooplankton productivity due to reductions in resource quality and volume of suitable habitat. Although these spatial comparisons provide an expectation for the response of zooplankton productivity as DOC concentration increases, we still have an incomplete understanding of how zooplankton respond to temporal increases in DOC concentration within a single system. As such, we used a whole‐lake manipulation, in which DOC concentration was increased from 8 to 11 mg L^?1 in one basin of a manipulated lake, to test the hypothesis that crustacean zooplankton production should subsequently decrease. In contrast to the spatially derived expectation of sharp DOC‐mediated decline, we observed a small increase in zooplankton densities in response to our experimental increase in DOC concentration of the treatment basin. This was due to significant increases in gross primary production and resource quality (lower seston carbon‐to‐phosphorus ratio; C:P). These results demonstrate that temporal changes in lake characteristics due to increased DOC may impact zooplankton in ways that differ from those observed in spatial surveys. We also identified significant interannual variability across our study region, which highlights potential difficulty in detecting temporal responses of organism abundances to gradual environmental change (e.g., browning).     

三江平原不同湿地类型土壤活性有机碳组分及含量差异

土壤活性有机碳对土壤干扰的反应较快,是土壤有机碳早期变化的敏感性指标。近50年来,三江平原湿地土壤有机碳库受农事活动影响较大。为了探讨不同湿地类型土壤活性有机碳主要组分土壤可溶性有机碳(Dissolved organic carbon,DOC)、微生物量碳(Microbial biomass carbon,MBC)和易氧化有机碳(Easily oxidized organic carbon,EOC)的分布差异及主要影响因子,选择了三江平原洪河自然保护区4种典型的湿地类型(小叶章+沼柳湿地、小叶章湿地、毛苔草湿地和芦苇湿地)为研究对象。分析了不同湿地类型土壤可溶性有机碳,微生物量碳和易氧化有机碳在0—30 cm土层内的分布特征和分配比例及其与有机碳、土壤养分和酶活性指标(蔗糖酶、纤维素酶和过氧化氢酶)之间的相关关系。结果表明:(1)4种湿地类型土壤DOC、MBC和EOC含量均随土层深度的增加而减少。不同湿地类型之间土壤活性有机碳含量在0—30 cm土层内存在显著性差异(P0.05),相对于长期淹水的毛苔草湿地和芦苇湿地而言,未淹水的小叶章+沼柳湿地和小叶章湿地具有较高的DOC,MBC和EOC含量。(2)土壤DOC、MBC和EOC占有机碳比例分别为0.27%—0.63%,1.27%—5.94%和19.63%—41.25%。土壤DOC所占比例呈先增后减的变化趋势,最大的比例均出现在10—20 cm。MBC所占比例在土壤剖面上则未表现出一致的变化规律,而EOC所占比例则随土层深度的增加而逐渐减少。(3)土壤DOC占SOC比例以小叶章湿地最高,MBC和EOC占SOC的比例则以小叶章+沼柳湿地最高。而长期淹水的毛苔草湿地和芦苇湿地则具有更低的DOC,MBC和EOC比例。(4)综合分析表明,4种湿地类型土壤DOC,MBC和EOC两两之间存在极显著相关性关系,它们除了与碳氮比相关性不显著外,与土壤有机碳,全氮,全磷养分和酶活性指标间相关性均达到极显著水平,尤其是与有机碳和全氮的相关性系数更高,此外DOC与纤维素酶,MBC与过氧化氢酶相关性更大。由此可见,土壤碳氮磷养分和酶活性是影响土壤活性有机碳组分分布的重要因素。     

氮添加对中国陆地生态系统植物-土壤碳动态的影响

近年来,中国大气氮沉降水平不断增加,过量的活性氮输入深刻影响了我国陆地生态系统碳循环。虽然已有大量的研究报道了模拟氮添加实验对我国陆地生态系统碳动态的影响,但是由于复杂的地理条件和不同的施氮措施,关于植物和土壤碳库对氮添加的一般响应特征和机制仍存在广泛争议。因此,采用整合分析方法,收集整理了172篇已发表的中国野外氮添加试验结果,在全国尺度上探究氮添加对我国陆地生态系统植物和土壤碳动态的影响及其潜在机制。结果表明,氮添加显著促进了植物的碳储存,地上和地下生物量均显著增加,且地上生物量比地下生物量增加得多。同时,氮添加显著增加了凋落物质量,但对细根生物量没有显著影响。氮添加显著降低了植物叶片、凋落物和细根的碳氮比。总体上,氮添加显著增加了土壤有机碳含量并降低了土壤pH值,但对可溶性有机碳、微生物生物量碳和土壤呼吸的影响并不显著。在不同的地理条件下,土壤有机碳含量对氮添加的响应呈现增加、减少或不变的不同趋势。回归分析表明,地上生物量与土壤有机碳含量之间,以及微生物生物量碳与土壤有机碳含量之间呈负相关关系。虽然氮添加通过增加凋落物质量显著促进了植物碳输入,但同时也会通过刺激微生物降解来增加土...     

Microbial dynamics and soil physicochemical properties explain large‐scale variations in soil organic carbon

First‐order organic matter decomposition models are used within most Earth System Models (ESMs) to project future global carbon cycling; these models have been criticized for not accurately representing mechanisms of soil organic carbon (SOC) stabilization and SOC response to climate change. New soil biogeochemical models have been developed, but their evaluation is limited to observations from laboratory incubations or few field experiments. Given the global scope of ESMs, a comprehensive evaluation of such models is essential using in situ observations of a wide range of SOC stocks over large spatial scales before their introduction to ESMs. In this study, we collected a set of in situ observations of SOC, litterfall and soil properties from 206 sites covering different forest and soil types in Europe and China. These data were used to calibrate the model MIMICS (The MIcrobial‐MIneral Carbon Stabilization model), which we compared to the widely used first‐order model CENTURY. We show that, compared to CENTURY, MIMICS more accurately estimates forest SOC concentrations and the sensitivities of SOC to variation in soil temperature, clay content and litter input. The ratios of microbial biomass to total SOC predicted by MIMICS agree well with independent observations from globally distributed forest sites. By testing different hypotheses regarding (using alternative process representations) the physicochemical constraints on SOC deprotection and microbial turnover in MIMICS, the errors of simulated SOC concentrations across sites were further decreased. We show that MIMICS can resolve the dominant mechanisms of SOC decomposition and stabilization and that it can be a reliable tool for predictions of terrestrial SOC dynamics under future climate change. It also allows us to evaluate at large scale the rapidly evolving understanding of SOC formation and stabilization based on laboratory and limited filed observation.     

温带森林不同海拔土壤有机碳及相关胞外酶活性特征

研究测定了老秃顶子温带森林生态系统7个海拔土壤不同形态碳和相关水解酶、氧化还原酶活性,分析了土壤有机碳及相关酶活性沿海拔梯度的影响因素.结果表明: 随海拔升高,土壤有机碳(SOC)、颗粒有机碳(POC)和可溶性有机碳(DOC)含量显著增加,而在海拔825～1233 m之间没有显著变化,DOC/SOC则显著下降;土壤α葡萄糖苷酶、β葡萄糖苷酶、木糖苷酶和纤维二糖水解酶活性显著增加;土壤SOC、POC、DOC、全氮(TN)含量及土壤含水量(SMC)与土壤水解酶活性呈显著正相关;过氧化物酶(POD)活性在低海拔(675 m)落叶松人工林显著低于其他海拔,POD活性与土壤碳氮(SOC、TN、POC、DOC)含量及SMC呈显著正相关,而土壤多酚氧化酶(PPO)活性在海拔947 m落叶阔叶林带和海拔825 m红松林中较高,且仅与土壤pH呈显著正相关,表明土壤酸度是驱动PPO酶活性的主要因素.在温带森林生态系统中,土壤养分含量和含水量是影响土壤水解酶海拔分布的重要因素.     

杉木人工林土壤可溶性有机质及其与土壤养分的关系

通过在福建省来舟林场对不同栽植代数杉木人工林土壤可溶性有机碳(DOC)和氮(DON)及土壤养分的研究,其结果表明,随着杉木栽植代数的增加林地土壤DOC和DON含量逐渐下降,在0～10cm土层内第3代杉木林土壤DOC和DON含量分别是第1代杉木林的83.9%和87.1%、第2代杉木林的90.6%和96.9%,在10～20cm土层内第3代杉木林土壤DOC和DON含量分别是第1代杉木林的80.2%和81.5%、第2代杉木林的81.8%和90.0%。在不同林地和土层内土壤DOC含量之间的差异性达到了显著或极显著水平,而DON含量之间的差异性不显著。不同栽植代数杉木林土壤养分的变化趋势与DOM一致,随着杉木连栽,土壤养分含量呈下降趋势。在0～10cm土层内第3代杉木林土壤全氮、全钾、铵态氮和速效钾含量分别是第1代杉木林的83.1%、60.4%、68.1%和44.3%,是第2代杉木林的84.6%、68.5%、74.4%和58.7%;在10～20cm土层内第3代杉木林土壤全氮、全钾、铵态氮和速效钾含量分别是第1代杉木林的74.0%、53.4%、57.6%和54.6%,是第2代杉木林的94.8%、59.5%、74.3%和65.5%。经相关性分析,在各土层内土壤DOC和DON含量与土壤全氮、全钾、铵态氮和速效钾等土壤养分含量存在着不同程度的相关性。