The carbon count of 2000 years of rice cultivation

More than 50% of the world's population feeds on rice. Soils used for rice production are mostly managed under submerged conditions (paddy soils). This management, which favors carbon sequestration, potentially decouples surface from subsurface carbon cycling. The objective of this study was to elucidate the long‐term rates of carbon accrual in surface and subsurface soil horizons relative to those of soils under nonpaddy management. We assessed changes in total soil organic as well as of inorganic carbon stocks along a 2000‐year chronosequence of soils under paddy and adjacent nonpaddy management in the Yangtze delta, China. The initial organic carbon accumulation phase lasts much longer and is more intensive than previously assumed, e.g., by the Intergovernmental Panel on Climate Change (IPCC). Paddy topsoils accumulated 170–178 kg organic carbon ha^?1 a^?1 in the first 300 years; subsoils lost 29–84 kg organic carbon ha^?1 a^?1 during this period of time. Subsoil carbon losses were largest during the first 50 years after land embankment and again large beyond 700 years of cultivation, due to inorganic carbonate weathering and the lack of organic carbon replenishment. Carbon losses in subsoils may therefore offset soil carbon gains or losses in the surface soils. We strongly recommend including subsoils into global carbon accounting schemes, particularly for paddy fields.     

Surficial gains and subsoil losses of soil carbon and nitrogen during secondary forest development

Reforestation of formerly cultivated land is widely understood to accumulate above‐ and belowground detrital organic matter pools, including soil organic matter. However, during 40 years of study of reforestation in the subtropical southeastern USA, repeated observations of above‐ and belowground carbon documented that significant gains in soil organic matter (SOM) in surface soils (0–7.5 cm) were offset by significant SOM losses in subsoils (35–60 cm). Here, we extended the observation period in this long‐term experiment by an additional decade, and used soil fractionation and stable isotopes and radioisotopes to explore changes in soil organic carbon and soil nitrogen that accompanied nearly 50 years of loblolly pine secondary forest development. We observed that accumulations of mineral soil C and N from 0 to 7.5 cm were almost entirely due to accumulations of light‐fraction SOM. Meanwhile, losses of soil C and N from mineral soils at 35 to 60 cm were from SOM associated with silt and clay‐sized particles. Isotopic signatures showed relatively large accumulations of forest‐derived carbon in surface soils, and little to no accumulation of forest‐derived carbon in subsoils. We argue that the land use change from old field to secondary forest drove biogeochemical and hydrological changes throughout the soil profile that enhanced microbial activity and SOM decomposition in subsoils. However, when the pine stands aged and began to transition to mixed pines and hardwoods, demands on soil organic matter for nutrients to support aboveground growth eased due to pine mortality, and subsoil organic matter levels stabilized. This study emphasizes the importance of long‐term experiments and deep measurements when characterizing soil C and N responses to land use change and the remarkable paucity of such long‐term soil data deeper than 30 cm.     

Sulfur in Ghanaian soils

Studies were carried out to examine factors which might influence the distribution of S in Ghanaian soils. Nine soil profiles developed over granitic rocks, three each representing the upper slope (US), middle slope (MS) and lower slope (LS) of catena in the evergreen high rain forest (ERF), semi-deciduous rain forest (SDF) and the interior savanna (ISAV) zone of Ghana were selected. The total S contents varied from 9 to 347 ppm; the average for all the surface and subsurface horizons was 141 ppm and for subsoils 105 ppm. The contents also varied according to: (1) the ecological zone as follows: ERF 0) SDF>ISAV and (2) the topographic position: US>MS>LS. The total S was closely correlated with organic C and total N in the surface and subsurface horizons (r=0.931^*** and 0.941^*** respectively). Inorganic sulfate was generally higher in the subsoils than in the surface and subsurface horizons of the ERF and SDF profiles whereas the opposite was the case in the ISAV profiles. Based on the critical value of 6 ppm in surface soils, all the savanna soils would be considered S deficient.The total organic S, which constituted from 56 to over 95% of the total S in the profiles, was significantly correlated with total N both in the surface and subsurface horizons (N:S ratio=9.1:1) and in the subsoils (N:S ratio=7.6:1). Fractionation of the organic S showed that HI-reducible S ranged from 14 to 117 ppm in the surface and subsurface horizons (average 55 ppm, equivalent to 47% of the total organic S) and from 2 to 169 ppm (average 55 ppm, equivalent to 60% of the total organic S) in the subsoils. The C-bonded S ranged from 6 to 223 ppm (average 73 ppm, equivalent to 57% of the total organic S) in the surface and subsurface horizons and from 1 to 83 ppm (average 29 ppm, equivalent to 32% of the total organic S) in the subsoils. HI-reducible S was significantly correlated with organic C (r=0.805^***) and total N (r=0.845^***) in the surface and subsurface horizons only whereas C-bonded S was significantly correlated with organic C and total N in both the surface and subsurface horizons and subsoils (r=0.870^*** and 0.624^*** respectively).The N:S ratios varied from 6.0 to 12.7 in the surface and subsurface horizons and from 0.5 to 27.3 in the subsoils. However the N:S ratio was less variable within the profile than the C:S ratio. The C:N:S ratios varied considerably within the profile and among the different soils but they fall within the range of values reported world-wide.     

Effect of land use change on soil carbon in Hawaii

Organic carbon storage and turnover were altered in soils formed from volcanic ash (Andisols) as a result of conversion of tropical forest to pasture and sugarcane cropland. Changes in soil carbon storage after approximately a century of each land use were estimated using stable carbon isotope values and carbon contents. Total organic carbon stored in soils varied as a result of management, with pasture soils showing net carbon gain and sugarcane soils showing net carbon loss. In pasture soils, increases in carbon at depth (40 to 80 cm) are below the rooting zone of the introduced (C4) vegetation, and have stable carbon isotopic values indicative of forest (C3) plants. Within the pasture rooting zone (0–40 cm) the isotopic data reveals that additions of pasture (C4) organic matter have been offset by losses of C3 carbon. The concentration of Fe/Al oxides (soil minerals that bind with organic matter to form oxide-humus complexes) appear to control the quantity of carbon stored in soils, as well as the difference in the depth and magnitude of carbon storage changes that occur with each type of land use change. Sugarcane land use appears to induce dissociation of Fe/Al oxide-humus complexes and loss of oxide-associated organic matter from the profile. In pastures, Fe/Al oxide-humus complexes are translocated to deeper horizons in the soils, resulting in greater profile carbon storage and longer apparent turnover time of carbon stored below 50 cm depth. In this high precipitation region, carbon losses from the soil appear to occur via downward transport, either as colloids or in solution, in addition to the generally assumed pathway of flux to the atmosphere as CO₂.     

Legacy effects of grassland management on soil carbon to depth

The importance of managing land to optimize carbon sequestration for climate change mitigation is widely recognized, with grasslands being identified as having the potential to sequester additional carbon. However, most soil carbon inventories only consider surface soils, and most large‐scale surveys group ecosystems into broad habitats without considering management intensity. Consequently, little is known about the quantity of deep soil carbon and its sensitivity to management. From a nationwide survey of grassland soils to 1 m depth, we show that carbon in grassland soils is vulnerable to management and that these management effects can be detected to considerable depth down the soil profile, albeit at decreasing significance with depth. Carbon concentrations in soil decreased as management intensity increased, but greatest soil carbon stocks (accounting for bulk density differences), were at intermediate levels of management. Our study also highlights the considerable amounts of carbon in subsurface soil below 30 cm, which is missed by standard carbon inventories. We estimate grassland soil carbon in Great Britain to be 2097 Tg C to a depth of 1 m, with ~60% of this carbon being below 30 cm. Total stocks of soil carbon (t ha^?1) to 1 m depth were 10.7% greater at intermediate relative to intensive management, which equates to 10.1 t ha^?1 in surface soils (0–30 cm), and 13.7 t ha^?1 in soils from 30 to 100 cm depth. Our findings highlight the existence of substantial carbon stocks at depth in grassland soils that are sensitive to management. This is of high relevance globally, given the extent of land cover and large stocks of carbon held in temperate managed grasslands. Our findings have implications for the future management of grasslands for carbon storage and climate mitigation, and for global carbon models which do not currently account for changes in soil carbon to depth with management.     

Black carbon accrual during 2000 years of paddy‐rice and non‐paddy cropping in the Yangtze River Delta,China

Rice straw burning has accompanied paddy management for millennia, introducing black carbon (BC) into soil as the residue of incomplete combustion. This study examined the contribution of BC to soil organic matter and the rate at which it accumulates in paddy soils as a result of prolonged paddy management. Soil depth profiles were sampled along a chronosequence of 0–2000 years of rice–wheat rotation systems and adjacent non‐paddy systems (50–700 years) in the Bay of Hangzhou (Zhejiang province, China). The soil BC content and its degree of condensation were assessed using benzene‐polycarboxylic acids (BPCAs) as geochemical markers. The results showed that despite regular long term BC input, BC only contributed 7–11% of total soil organic carbon (SOC) in the topsoil horizons. Nevertheless, along with SOC, paddy soils accumulated BC with increasing duration of management until 297 years to reach a steady‐state of 13 t BC ha^?1. This was 1.8 times more than in non‐paddy soils. The fate of BC in paddy soils (0–1 m) could be modeled revealing an average annual input of 44 kg ha^?1 yr^?1, and a mean residence time of 303 years. The subsoils contributed at least 50% to overall BC stocks, which likely derived from periods prior to land embankment and episodic burial of ancient topsoil, as also indicated by BPCA pattern changes. We conclude that there is a significant but limited accumulation of C in charred forms upon prolonged paddy management. The final contribution of BC to total SOC in paddy soils was similar to that in other aerobic ecosystems of the world.     

Accumulation of nitrogen and microbial residues during 2000 years of rice paddy and non‐paddy soil development in the Yangtze River Delta,China

Lowland rice paddy soils may accumulate significant amounts of organic matter. Our aim was to investigate the role of prolonged paddy management on the nitrogen (N) status of the soils, and to elucidate the contribution of bacteria and fungi to long‐term N accumulation processes. For this purpose, we sampled a chronosequence of 0–2000 years of rice cropping with adjacent non‐paddy systems in the Bay of Hangzhou, China. The samples were analyzed for bulk density, total, mineral and microbial N (N_mic), and amino sugars as markers for microbial residues. The results showed that during the first 100 years of land embankment, both paddy and non‐paddy soils accumulated N at a rate of up to 61 and 77 kg ha^?1 per annum, reaching steady‐state conditions after 110–172 years, respectively. Final N stocks in paddy fields exceeded those of the non‐paddies by a factor of 1.3. The contribution of amino sugars to total N increased to a maximum of 34 g N kg^?1 N in both land‐use systems, highlighting a significant accumulation of N in microbial residues of the surface soils. Correspondingly, the ratio of N_mic to microbial residue‐N decreased to a constant value. In the paddy subsoils, we found that bacterial residues particularly contributed to the pool of microbial residue‐N. Nevertheless, the absolute contents of amino sugars in paddy subsoils decreased during the last 1700 years of the chronosequence. We conclude that under paddy cultivation, soil microorganisms may accumulate parts of this N in their residues despite low overall N availability. However, this N accumulation is limited to initial stages of paddy soil development and restricted to the surface horizons, thus challenging its sustainability with future land‐use changes.     

Soil phosphorus does not keep pace with soil carbon and nitrogen accumulation following woody encroachment

Soil carbon, nitrogen, and phosphorus cycles are strongly interlinked and controlled through biological processes, and the phosphorus cycle is further controlled through geochemical processes. In dryland ecosystems, woody encroachment often modifies soil carbon, nitrogen, and phosphorus stores, although it remains unknown if these three elements change proportionally in response to this vegetation change. We evaluated proportional changes and spatial patterns of soil organic carbon (SOC), total nitrogen (TN), and total phosphorus (TP) concentrations following woody encroachment by taking spatially explicit soil cores to a depth of 1.2 m across a subtropical savanna landscape which has undergone encroachment by Prosopis glandulosa (an N₂ fixer) and other woody species during the past century in southern Texas, USA. SOC and TN were coupled with respect to increasing magnitudes and spatial patterns throughout the soil profile following woody encroachment, while TP increased slower than SOC and TN in topmost surface soils (0–5 cm) but faster in subsurface soils (15–120 cm). Spatial patterns of TP strongly resembled those of vegetation cover throughout the soil profile, but differed from those of SOC and TN, especially in subsurface soils. The encroachment of woody species dominated by N₂‐fixing trees into this P‐limited ecosystem resulted in the accumulation of proportionally less soil P compared to C and N in surface soils; however, proportionally more P accrued in deeper portions of the soil profile beneath woody patches where alkaline soil pH and high carbonate concentrations would favor precipitation of P as relatively insoluble calcium phosphates. This imbalanced relationship highlights that the relative importance of biotic vs. abiotic mechanisms controlling C and N vs. P accumulation following vegetation change may vary with depth. Our findings suggest that efforts to incorporate effects of land cover changes into coupled climate–biogeochemical models should attempt to represent C‐N‐P imbalances that may arise following vegetation change.     

Carbon cycling in eroding landscapes: geomorphic controls on soil organic C pool composition and C stabilization

Recent studies have highlighted the tight coupling between geomorphic processes and soil carbon (C) turnover and suggested that eroding landscapes can stabilize more C than their non‐eroding counterparts. However, large uncertainties remain and a mechanistic understanding of geomorphic effects on C storage in soils is still lacking. Here, we quantified the soil organic carbon (SOC) stock and pool distribution along geomorphic gradients and combined data derived from soil organic matter fractionation and incubation experiments. The size and composition of the SOC pools were strongly related to geomorphic position: 1.6 to 6.2 times more C was stabilized in the subsoils (25–100cm) of depositional profiles than in those of eroding profiles. Subsoil C of depositional profiles is predominantly associated with microaggregates and silt‐sized particles which are associated with pools of intermediate stability. We observed a significantly higher mean residence time for the fast and intermediate turnover pools of buried C at depositional positions, relative to non‐eroding and eroding positions, resulting from the physical protection of C associated with microaggregates and silt particles. Conversely, significant amounts of C were replaced at eroding positions but the lower degree of decomposition and the lack of physically protected C, resulted in higher respiration rates. By considering C cycling at non‐eroding, eroding and depositional positions, we found that the eroding landscapes studied store up to 10% more C due to soil redistribution processes than non‐eroding landscapes. This is the result of the stabilization of C in former subsoil at eroding positions and partial preservation of buried C in pools of intermediate turnover at depositional positions. However, the sink strength was limited by significant losses of buried C as only a small fraction of the C was associated with stable pools.     

Impact of Agricultural Land-use Change on Carbon Storage in Boreal Alaska

Climate warming is most pronounced at high latitudes, which could result in the intensification of the extensively cultivated areas in the boreal zone and could further enhance rates of forest clearing in the coming decades. Using paired forest‐field sampling and a chronosequence approach, we investigated the effect of conversion of boreal forest to agriculture on carbon (C) and nitrogen (N) dynamics in interior Alaska. Chronosequences showed large soil C losses during the first two decades following deforestation, with mean C stocks in agricultural soils being 44% or 8.3 kg m^?2 lower than C stocks in original forest soils. This suggests that soil C losses from land‐use change in the boreal region may be greater than those in other biomes. Analyses of changes in stable C isotopes and in quality of soil organic matter showed that organic C was lost from soils by combustion of cleared forest material, decomposition of organic matter and possibly erosion. Chronosequences indicated an increase in C storage during later decades after forest clearing, with 60‐year‐old grassland showing net ecosystem C gain of 2.1 kg m^?2 over the original forest. This increase in C stock resulted probably from a combination of large C inputs from belowground biomass and low C losses due to a small original forest soil C stock and low tillage frequency. Reductions in soil N stocks caused by land‐use change were smaller than reductions in C stocks (34% or 0.31 kg m^?2), resulting in lower C/N ratios in field compared with forest mineral soils, despite the occasional incorporation of high‐C forest‐floor material into field soils. Carbon mineralization per unit of mineralized N was considerably higher in forests than in fields, which could indicate that decomposition rates are more sensitive in forest soils than in field soils to inorganic N addition (e.g. by increased N deposition from the atmosphere). If forest conversion to agriculture becomes more widespread in the boreal region, the resulting C losses (51% or 11.2 kg m^?2 at the ecosystem level in this study) will induce a positive feedback to climatic warming and additional land‐use change. However, by selecting relatively C‐poor soils and by implementing management practices that preserve C, losses of C from soils can be reduced.     

Land use induced changes of organic carbon storage in soils of China

Using the data compiled from China's second national soil survey and an improved method of soil carbon bulk density, we have estimated the changes of soil organic carbon due to land use, and compared the spatial distribution and storage of soil organic carbon (SOC) in cultivated soils and noncultivated soils in China. The results reveal that ～ 57% of the cultivated soil subgroups ( ～ 31% of the total soil surface) have experienced a significant carbon loss, ranging from 40% to 10% relative to their noncultivated counterparts. The most significant carbon loss is observed for the non‐irrigated soils (dry farmland) within a semiarid/semihumid belt from northeastern to southwestern China, with the maximum loss occurring in northeast China. On the contrary, SOC has increased in the paddy and irrigated soils in northwest China. No significant change is observed for forest soils in southern China, grassland and desert soils in northwest China, as well as irrigated soils in eastern China. The SOC storage and density under noncultivated conditions in China are estimated to ～ 77.4 Pg (10¹⁵ g) and ～ 8.8 kg C m^?2, respectively, compared to a SOC storage of ～ 70.3 Pg and an average SOC density of ～ 8.0 kg C m^?2 under the present‐day conditions. This suggests a loss of ～ 7.1 Pg SOC and a decrease of ～ 0.8 kg C m^?2 SOC density due to increasing human activities, in which the loss in organic horizons has contributed to ～ 77%. This total loss of SOC in China induced by land use represents ～ 9.5% of the world's SOC decrease. This amount is equivalent to ～ 3.5 ppmv of the atmospheric CO₂ increase. Since ～ 78% of the currently cultivated soils in China have been degraded to a low/medium productivities and are responsible for most of the SOC loss, an improved land management, such as the development of irrigated and paddy land uses, would have a considerable potential in restoring the SOC storage. Assuming a restoration of ～ 50% of the lost SOC during the next 20–50 years, the soils in China would absorb ～ 3.5 Pg of carbon from the atmosphere.     

Carbon sequestration potential of soils in southeast Germany derived from stable soil organic carbon saturation

Sequestration of atmospheric carbon (C) in soils through improved management of forest and agricultural land is considered to have high potential for global CO₂ mitigation. However, the potential of soils to sequester soil organic carbon (SOC) in a stable form, which is limited by the stabilization of SOC against microbial mineralization, is largely unknown. In this study, we estimated the C sequestration potential of soils in southeast Germany by calculating the potential SOC saturation of silt and clay particles according to Hassink [Plant and Soil 191 (1997) 77] on the basis of 516 soil profiles. The determination of the current SOC content of silt and clay fractions for major soil units and land uses allowed an estimation of the C saturation deficit corresponding to the long‐term C sequestration potential. The results showed that cropland soils have a low level of C saturation of around 50% and could store considerable amounts of additional SOC. A relatively high C sequestration potential was also determined for grassland soils. In contrast, forest soils had a low C sequestration potential as they were almost C saturated. A high proportion of sites with a high degree of apparent oversaturation revealed that in acidic, coarse‐textured soils the relation to silt and clay is not suitable to estimate the stable C saturation. A strong correlation of the C saturation deficit with temperature and precipitation allowed a spatial estimation of the C sequestration potential for Bavaria. In total, about 395 Mt CO₂‐equivalents could theoretically be stored in A horizons of cultivated soils – four times the annual emission of greenhouse gases in Bavaria. Although achieving the entire estimated C storage capacity is unrealistic, improved management of cultivated land could contribute significantly to CO₂ mitigation. Moreover, increasing SOC stocks have additional benefits with respect to enhanced soil fertility and agricultural productivity.     

重庆岩溶区土壤有机碳库的估算及其空间分布特征

基于重庆市第二次土壤普查和2007年测土配方施肥的1 412个土壤剖面数据,结合重庆岩溶区土壤图、土地利用现状图和行政区划图,在地理信息系统技术的支持下,对重庆岩溶区土壤有机碳密度及储量进行了估算,同时引入有机碳丰度指数这一指标,对有机碳在不同土壤和不同景观中的分布特征进行了分析.结果表明:重庆岩溶区20 cm和100 cm深度的土壤有机碳储量分别为1.43×1011 kg和3.29×1011 kg.不同土地利用方式下重庆岩溶区土壤有机碳密度分布不均匀,20 cm深度的土壤有机碳密度介于1.26～7.20 kg m-2之间,100 cm深度的土壤有机碳密度介于1.43～25.72 kg m-2之间.重庆岩溶区土壤有机碳库在不同土壤和不同景观中的分布具有高度的空间变异性,20 cm深度的土壤和景观有机碳丰度指数分别在0.73～1.74和0.39～1.20之间,100 cm深度的土壤和景观有机碳丰度指数分别在0.32～3.00和0.46～1.70之间.与全国的平均水平相比,单位面积上20 cm深度土壤有机碳储量重庆岩溶区高于全国的平均水平,但单位面积上100 cm深度土壤有机碳储量重庆岩溶区低于全国的平均水平,总体而言,重庆岩溶区是土壤有机碳储量相对贫乏的区域.     

可溶性有机碳在米槠天然林不同土层中的迁移特征

选取我国中亚热带典型的常绿阔叶林米槠天然林(Castanopsis carlesii)为研究对象,采集林内米槠凋落物并通过挖剖面法分6个土层采集土样至1m。通过浸提米槠凋落物得到可溶性有机碳(dissolved organic carbon,DOC)溶液并在室内模拟其在不同土层的淋溶过程,不仅分析了土壤性质对DOC淋溶的影响,还研究了淋溶前后DOC化学结构的变化,以阐明DOC在不同土层中的迁移特征及影响因素,探寻米槠天然林土壤的固碳潜力和DOC在土壤有机碳循环中的作用。结果表明:(1)下层土壤比上层土壤吸附DOC的能力更强,亲水性DOC与疏水性DOC间会争夺土壤颗粒表面的吸附位点,而且芳香化合物和大分子物质等疏水性DOC组分会被优先吸附;(2)红外光谱表明,芳香类和醚类等疏水性物质会优先被吸附,烷烃类物质却不易被吸附,土壤中原有的酚、醇类亲水性物质会被初始DOC中的疏水性物质置换出来;(3)土壤DOC的截留能力与粘粒、游离氧化铁含量呈极显著正相关,而与土壤有机碳和砂粒含量呈极显著负相关,其中土壤有机碳的含量是影响米槠天然林不同土层DOC截留量的关键因素。     

Effects of wildfire and permafrost on soil organic matter and soil climate in interior Alaska

The influence of discontinuous permafrost on ground‐fuel storage, combustion losses, and postfire soil climates was examined after a wildfire near Delta Junction, AK in July 1999. At this site, we sampled soils from a four‐way site comparison of burning (burned and unburned) and permafrost (permafrost and nonpermafrost). Soil organic layers (which comprise ground‐fuel storage) were thicker in permafrost than nonpermafrost soils both in burned and unburned sites. While we expected fire severity to be greater in the drier site (without permafrost), combustion losses were not significantly different between the two burned sites. Overall, permafrost and burning had significant effects on physical soil variables. Most notably, unburned permafrost sites with the thickest organic mats consistently had the coldest temperatures and wettest mineral soil, while soils in the burned nonpermafrost sites were warmer and drier than the other soils. For every centimeter of organic mat thickness, temperature at 5 cm depth was about 0.5°C cooler during summer months. We propose that organic soil layers determine to a large extent the physical and thermal setting for variations in vegetation, decomposition, and carbon balance across these landscapes. In particular, the deep organic layers maintain the legacies of thermal and nutrient cycling governed by fire and revegetation. We further propose that the thermal influence of deep organic soil layers may be an underlying mechanism responsible for large regional patterns of burning and regrowth, detected in fractal analyses of burn frequency and area. Thus, fractal geometry can potentially be used to analyze changes in state of these fire prone systems.     

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.     

Soil organic carbon content and composition of 130-year crop, pasture and forest land-use managements

Conversion of former agricultural land to grassland and forest ecosystems is a suggested option for mitigation of increased atmospheric CO₂. A Sharpsburg prairie loess soil (fine, smectitic, mesic Typic Argiudoll) provided treatments to study the impact of long‐term land use on soil organic carbon (SOC) content and composition for a 130‐year‐old cropped, pasture and forest comparison. The forest and pasture land use significantly retained more SOC, 46% and 25%, respectively, compared with cropped land use, and forest land use increased soil C content by 29% compared with the pasture. Organic C retained in the soils was a function of the soil N content (r=0.98, P<0.001) and the soil carbohydrate (CH) concentration (r=0.96, P<0.001). Statistical analyses found that soil aggregation processes increased as organic C content increased in the forest and pasture soils, but not in the cropped soil. SOC was composed of similar percentages of CHs (49%, 42% and 51%), amino acids (22%, 15% and 18%), lipids (2.3%, 2.3% and 2.9%) and unidentified C (21%, 29% and 27%), but differed for phenolic acids (PAs) (5.7%, 11.6% and 1.0%) for the pasture, forest and cropped soils, respectively. The results suggested that the majority of the surface soil C sequestered in the long‐term pasture and forest soils was identified as C of plant origin through the use of CH and PA biomarkers, although the increase in amino sugar concentration of microbial origin indicates a greater increase in microbial inputs in the three subsoils. The practice of permanent pastures and afforestation of agricultural land showed long‐term potential for potential mitigation of atmospheric CO₂.     

Deep ploughing increases agricultural soil organic matter stocks

Subsoils play an important role within the global C cycle, since they have high soil organic carbon (SOC) storage capacity due to generally low SOC concentrations. However, measures for enhancing SOC storage commonly focus on topsoils. This study assessed the long‐term storage and stability of SOC in topsoils buried in arable subsoils by deep ploughing, a globally applied method for breaking up hard pans and improving soil structure to optimize crop growing conditions. One effect of deep ploughing is translocation of SOC formed near the surface into the subsoil, with concomitant mixing of SOC‐poor subsoil material into the ‘new’ topsoil. Deep‐ploughed croplands represent unique long‐term in situ incubations of SOC‐rich material in subsoils. In this study, we sampled five loamy and five sandy soils that were ploughed to 55–90 cm depth 35–50 years ago. Adjacent, similarly managed but conventionally ploughed subplots were sampled as reference. The deep‐ploughed soils contained on average 42 ± 13% more SOC than the reference subplots. On average, 45 years after deep ploughing, the ‘new’ topsoil still contained 15% less SOC than the reference topsoil, indicating long‐term SOC accumulation potential in the topsoil. In vitro incubation experiments on the buried sandy soils revealed 63 ± 6% lower potential SOC mineralisation rates and also 67 ± 2% lower SOC mineralisation per unit SOC in the buried topsoils than in the reference topsoils. Wider C/N ratio in the buried sandy topsoils than in the reference topsoils indicates that deep ploughing preserved SOC. The SOC mineralisation per unit SOC in the buried loamy topsoils was not significantly different from that in the reference topsoils. However, 56 ± 4% of the initial SOC was preserved in the buried topsoils. It can be concluded that deep ploughing contributes to SOC sequestration by enlarging the storage space for SOC‐rich material.     

Increased soil carbon storage through plant diversity strengthens with time and extends into the subsoil

Soils are important for ecosystem functioning and service provisioning. Soil communities and their functions, in turn, are strongly promoted by plant diversity, and such positive effects strengthen with time. However, plant diversity effects on soil organic matter have mostly been investigated in the topsoil, and there are only very few long-term studies. Thus, it remains unclear if plant diversity effects strengthen with time and to which depth these effects extend. Here, we repeatedly sampled soil to 1 m depth in a long-term grassland biodiversity experiment. We investigated how plant diversity impacted soil organic carbon and nitrogen concentrations and stocks and their stable isotopes ¹³C and ¹⁵N, as well as how these effects changed after 5, 10, and 14 years. We found that higher plant diversity increased carbon and nitrogen storage in the topsoil since the establishment of the experiment. Stable isotopes revealed that these increases were associated with new plant-derived inputs, resulting in less processed and less decomposed soil organic matter. In subsoils, mainly the presence of specific plant functional groups drove organic matter dynamics. For example, the presence of deep-rooting tall herbs decreased carbon concentrations, most probably through stimulating soil organic matter decomposition. Moreover, plant diversity effects on soil organic matter became stronger in topsoil over time and reached subsoil layers, while the effects of specific plant functional groups in subsoil progressively diminished over time. Our results indicate that after changing the soil system the pathways of organic matter transfer to the subsoil need time to establish. In our grassland system, organic matter storage in subsoils was driven by the redistribution of already stored soil organic matter from the topsoil to deeper soil layers, for example, via bioturbation or dissolved organic matter. Therefore, managing plant diversity may, thus, have significant implications for subsoil carbon storage and other critical ecosystem services.     

Factors Affecting Degradation of Aldicarb and Ethoprop

Chemical and microbial degradation of the nematicides-insecticides aldicarb and ethoprop has been studied extensively in both laboratory and field studies. These studies show that temperature is the most important variable affecting the degradation rate of aldicarb and its carbamate metabolites in surface soils. Temperature and organic matter appear to be the most important variables affecting degradation rates of ethoprop in soils under normal agricultural conditions, with organic matter being inversely related to degradation, presumably due to increased binding to soil particles. Soil moisture may be important under some conditions for both compounds, with degradation reduced in low-moisture soils. The rate of degradation of aldicarb residues (aldicarb + aldicarb sulfoxide + aldicarb sulfone) does not seem to be significantly affected by depth from soil surface, except that aldicarb residues degrade more slowly in acidic, coarse sand subsoils. Degradation of ethoprop also continues in subsurface soils, although field data are limited due to its lower mobility. Both compounds degrade in groundwater. Because microbial activity decreases with depth below soil surface, chemical processes are important components of the degradation of both aldicarb residues and ethoprop. For aldicarb, transformation to carbamate oxides in surface soils is primarily microbial, while degradation to noncarbamate compounds appears to be primarily the result of soil-catalyzed hydrolysis throughout the soil profile. For ethoprop, both chemical and microbial catalyzed hydrolysis are important in surface soils, with chemical hydrolysis becoming more important with increasing depth.