Enhancement of Carbon Sequestration in Soil in the Temperature Grasslands of Northern China by Addition of Nitrogen and Phosphorus

Increased nitrogen (N) deposition is common worldwide. Questions of where, how, and if reactive N-input influences soil carbon (C) sequestration in terrestrial ecosystems are of great concern. To explore the potential for soil C sequestration in steppe region under N and phosphorus (P) addition, we conducted a field experiment between 2006 and 2012 in the temperate grasslands of northern China. The experiment examined 6 levels of N (0–56 g N m^-2 yr^-1), 6 levels of P (0–12.4 g P m^-2 yr^-1), and a control scenario. Our results showed that addition of both N and P enhanced soil total C storage in grasslands due to significant increases of C input from litter and roots. Compared with control plots, soil organic carbon (SOC) in the 0–100 cm soil layer varied quadratically, from 156.8 to 1352.9 g C m^-2 with N addition gradient (R² = 0.99, P < 0.001); and logarithmically, from 293.6 to 788.6 g C m^-2 with P addition gradient (R² = 0.56, P = 0.087). Soil inorganic carbon (SIC) decreased quadratically with N addition. The net C sequestration on grassland (including plant, roots, SIC, and SOC) increased linearly from -128.6 to 729.0 g C m^-2 under N addition (R² = 0.72, P = 0.023); and increased logarithmically, from 248.5 to 698 g C m^-2under P addition (R² = 0.82, P = 0.014). Our study implies that N addition has complex effects on soil carbon dynamics, and future studies of soil C sequestration on grasslands should include evaluations of both SOC and SIC under various scenarios.     

Soil inorganic carbon storage pattern in China

Soils with pedogenic carbonate cover about 30% (3.44 × 10⁶ km²) of China, mainly across its arid and semiarid regions in the Northwest. Based on the second national soil survey (1979–1992), total soil inorganic carbon (SIC) storage in China was estimated to be 53.3±6.3 PgC (1 Pg=10¹⁵ g) to the depth investigated to 2 m. Soil inorganic carbon storages were 4.6, 10.6, 11.1, and 20.8 Pg for the depth ranges of 0–0.1, 0.1–0.3, 0.3–0.5, and 0.5–1 m, respectively. Stocks for 0.1, 0.3, 0.5, and 1 m of depth accounted for 8.7%, 28.7%, 49.6%, and 88.9% of total SIC, respectively. In contrast with soil organic carbon (SOC) storage, which is highest under 500–800 mm yr⁻¹ of mean precipitation, SIC storage peaks where mean precipitation is <400 mm yr⁻¹. The amount and vertical distribution of SIC was related to climate and land cover type. Content of SIC in each incremental horizon was positively related with mean annual temperature and negatively related with mean annual precipitation, with the magnitude of SIC content across land cover types showing the following order: desert, grassland >shrubland, cropland >marsh, forest, meadow. Densities of SIC increased generally with depth in all ecosystem types with the exception of deserts and marshes where it peaked in intermediate layers (0.1–0.3 m for first and 0.3–0.5 m for latter). Being an abundant component of soil carbon stocks in China, SIC dynamics and the process involved in its accumulation or loss from soils require a better understanding.     

Widespread decreases in topsoil inorganic carbon stocks across China's grasslands during 1980s–2000s

Soil carbon (C) stocks consist of inorganic and organic components, ~1.7 times larger than the total of the C stored in vegetation and the atmosphere together. Significant soil C losses could thus offset any C sink in vegetation, creating a positive feedback to climate change. However, compared with the susceptible sensitivity of organic matter decay to climate warming, soil inorganic carbon (SIC) stocks are often assumed to be relatively stable. Here, we evaluated SIC changes across China's grasslands over the last two decades using data from a recent regional soil survey during 2001–2005 and historical national soil inventory during the 1980s. Our results showed that SIC stocks in the top 10 cm decreased significantly between the two sampling periods, with a mean rate of 26.8 (95% confidence interval: 15.8–41.7) g C m^?2 yr^?1. The larger decreases in SIC stocks were observed in those regions with stronger soil acidification and richer soil carbonates. The lost SIC could be released to the atmosphere as carbon dioxide, redistributed to the deeper soil layer, and transferred to the nearby regions. The fraction of soil carbonates entering into the atmosphere may diminish the strength of terrestrial C sequestration and amplify the positive C‐climate feedback.     

Dissolved carbon leaching from soil is a crucial component of the net ecosystem carbon balance

Estimates of carbon leaching losses from different land use systems are few and their contribution to the net ecosystem carbon balance is uncertain. We investigated leaching of dissolved organic carbon (DOC), dissolved inorganic carbon (DIC), and dissolved methane (CH₄), at forests, grasslands, and croplands across Europe. Biogenic contributions to DIC were estimated by means of its δ¹³C signature. Leaching of biogenic DIC was 8.3±4.9 g m^?2 yr^?1 for forests, 24.1±7.2 g m^?2 yr^?1 for grasslands, and 14.6±4.8 g m^?2 yr^?1 for croplands. DOC leaching equalled 3.5±1.3 g m^?2 yr^?1 for forests, 5.3±2.0 g m^?2 yr^?1 for grasslands, and 4.1±1.3 g m^?2 yr^?1 for croplands. The average flux of total biogenic carbon across land use systems was 19.4±4.0 g C m^?2 yr^?1. Production of DOC in topsoils was positively related to their C/N ratio and DOC retention in subsoils was inversely related to the ratio of organic carbon to iron plus aluminium (hydr)oxides. Partial pressures of CO₂ in soil air and soil pH determined DIC concentrations and fluxes, but soil solutions were often supersaturated with DIC relative to soil air CO₂. Leaching losses of biogenic carbon (DOC plus biogenic DIC) from grasslands equalled 5–98% (median: 22%) of net ecosystem exchange (NEE) plus carbon inputs with fertilization minus carbon removal with harvest. Carbon leaching increased the net losses from cropland soils by 24–105% (median: 25%). For the majority of forest sites, leaching hardly affected actual net ecosystem carbon balances because of the small solubility of CO₂ in acidic forest soil solutions and large NEE. Leaching of CH₄ proved to be insignificant compared with other fluxes of carbon. Overall, our results show that leaching losses are particularly important for the carbon balance of agricultural systems.     

Root turnover as determinant of the cycling of C,N, and P in a dry heathland ecosystem

Root production and turnover were studied using sequential core sampling and observations in permanent minirhizotrons in the field in three dry heathland stands dominated by the evergreen dwarfshrub Calluna vulgaris and the grasses Deschampsia flexuosa and Molinia caerulea, respectively. Root biomass production, estimated by core sampling, amounted to 160 (Calluna), 180 (Deschampsia) and 1380 (Molinia) g m^-2 yr^-1, respectively. Root biomass turnover rate in Calluna (0.64 yr^-1) was lower compared with the grasses (Deschampsia: 0.96 yr^-1; Molinia 1.68yr^-1)). Root length turnover rate was 0.75–0.77 yr^-1 (Deschampsia) and 1.17–1.49 yr^-1 (Molinia), respectively. No resorption of N and P from senescing roots was observed in either species. Input of organic N into the soil due to root turnover, estimated using the core sampling data, amounted to 1.8 g N m^-2 yr^-1(^Calluna), 1.7 g N m^-2 yr^-1 (Deschampsia) and 19.7 g N m^-2 yr^-1 (Molinia), respectively. The organic P input was 0.05, 0.07 and 0.55 g P M^-2 yr^-1, respectively. Using the minirhizotron turnover estimates these values were20–22% (Deschampsia) and 11–30% (Molinia) lower.When the biomass turnover data were used, it appeared that in the Molinia stand root turnover contributed 67% to total litter production, 87% to total litter nitrogen loss and 84% to total litter phosphorus loss. For Calluna and Deschampsia these percentages were about three and two times lower, respectively.This study shows that (1) Root turnover is a key factor in ecosystem C, N, and P cycling; and that (2) The relative importance of root turnover differs between species.     

Terrestrial nitrogen cycle simulation with a dynamic global vegetation model

A global scale Dynamic Nitrogen scheme (DyN) has been developed and incorporated into the Lund–Posdam–Jena (LPJ) dynamic global vegetation model (DGVM). The DyN is a comprehensive process‐based model of the cycling of N through and within terrestrial ecosystems, with fully interactive coupling to vegetation and C dynamics. The model represents the uptake, allocation and turnover of N in plants, and soil N transformations including mineralization, N₂ fixation, nitrification and denitrification, NH₃ volatilization, N leaching, and N₂, N₂O and NO production and emission. Modelled global patterns of site‐scale nitrogen fluxes and reservoirs are highly correlated to observations reported from different biomes. The simulation of site‐scale net primary production and soil carbon content was improved relative to the original LPJ, which lacked an interactive N cycle, especially in the temporal and boreal regions. Annual N uptake by global natural vegetation was simulated as 1.084 Pg N yr⁻¹, with lowest values <1 g N m⁻² yr⁻¹ (polar desert) and highest values in the range 24–36.5 g N m⁻² yr⁻¹ (tropical forests). Simulated global patterns of annual N uptake are consistent with previous model results by Melillo et al. The model estimates global total nitrogen storage potentials in vegetation (5.3 Pg N), litter (4.6 Pg N) and soil (≥67 Pg as organic N and 0.94 Pg as inorganic N). Simulated global patterns of soil N storage are consistent with the analysis by Post et al. although total simulated N storage is less. Deserts were simulated to store 460 Tg N (up to 0.262 kg N m⁻²) as NO₃⁻, contributing 80% of the global total NO₃⁻ inventory of 580 Tg N. This model result is in agreement with the findings of a large NO₃⁻ pool beneath deserts. Globally, inorganic soil N is a small reservoir, comprising only 1.6% of the global soil N content to 1.5 m soil depth, but the ratio has a very high spatial variability and in hot desert regions, inorganic NO₃⁻ is estimated to be the dominant form of stored N in the soil.     

Carbon dioxide consumption during soil development

Carbon is sequestered in soils by accumulation of recalcitrant organic matter and by bicarbonate weathering of silicate minerals. Carbon fixation by ecosystems helps drive weathering processes in soils and that in turn diverts carbon from annual photosynthesis-soil respiration cycling into the long-term geological carbon cycle. To quantify rates of carbon transfer during soil development in moist temperate grassland and desert scrubland ecosystems, we measured organic and inorganic residues derived from the interaction of soil biota and silicate mineral weathering for twenty-two soil profiles in arkosic sediments of differing ages. In moist temperate grasslands, net annual removal of carbon from the atmosphere by organic carbon accumulation and silicate weathering ranges from about 8.5 g m^–2 yr^–1 for young soils to 0.7 g M^–2 yr^–1 for old soils. In desert scrublands, net annual carbon removal is about 0.2 g m^–2 yr^–1 for young soils and 0.01 g m^–2 yr^–1 for old soils. In soils of both ecosystems, organic carbon accumulation exceeds CO₂ removal by weathering, however, as soils age, rates of CO₂ consumption by weathering accounts for greater amounts of carbon sequestration, increasing from 2% to 8% in the grassland soils and from 2% to 40% in the scrubland soils. In soils of desert scrublands, carbonate accumulation far outstrips organic carbon accumulation, but about 90% of this mass is derived from aerosolic sources that do not contribute to long-term sequestration of atmospheric carbon dioxide.     

Effect of Vegetation Rehabilitation on Soil Carbon and Its Fractions in Mu Us Desert,Northwest China

Although vegetation rehabilitation on semi-arid and arid regions may enhance soil carbon sequestration, its effects on soil carbon fractions remain uncertain. We carried out a study after planting Artemisia ordosica (AO, 17 years), Astragalus mongolicum (AM, 5 years), and Salix psammophila (SP, 16 years) on shifting sand land (SL) in the Mu Us Desert, northwest China. We measured total soil carbon (TSC) and its components, soil inorganic carbon (SIC) and soil organic carbon (SOC), as well as the light and heavy fractions within soil organic carbon (LF-SOC and HF-SOC), under the SL and shrublands at depths of 100 cm. TSC stock under SL was 27.6 Mg ha^?1, and vegetation rehabilitation remarkably elevated it by 40.6 Mgha^?1, 4.5 Mgha^?1, and 14.1 Mgha^?1 under AO, AM and SP land, respectively. Among the newly formed TSC under the three shrublands, SIC, LF-SOC and HF-SOC accounted for 75.0%, 10.7% and 13.1% for AO, respectively; they made up 37.0%, 50.7% and 10.6% for AM, respectively; they occupied 68.6%, 18.8% and 10.0% for SP, respectively. The accumulation rates of TSC within 0–100 cm reached 238.6 g m^?2y^?1, 89.9 g m^?2y^?1 and 87.9 g m^?2y^?1 under AO, AM and SP land, respectively. The present study proved that the accumulation of SIC considerably contributed to soil carbon sequestration, and vegetation rehabilitation on shifting sand land has a great potential for soil carbon sequestration.     

Climate warming increases soil erosion,carbon and nitrogen loss with biofuel feedstock harvest in tallgrass prairie

Anthropogenic soil erosion severely affects land ecosystems by reducing plant productivity and stimulating horizontal carbon and nitrogen movement at the surface. Climate warming may accelerate soil erosion by altering soil temperature, moisture, and vegetation coverage. However, no experiments have been carried out to quantify soil erosion with warming. In a long‐term field experiment, we explored how annual clipping for biofuel feedstock production and warming caused soil erosion and accompanying carbon and nitrogen losses in tallgrass prairie in Oklahoma, USA. We measured relative changes in soil surface elevation between clipped and unclipped plots with or without experimental warming. Our results show that average relative erosion depth caused by clipping was 1.65±0.09 and 0.54±0.08 mm yr^?1, respectively, in warmed and control plots from November 21, 1999 to April 21, 2009. The soil erosion rate was 2148±121 g m^?2 yr^?1 in the warmed plots and 693±113 g m^?2 yr^?1 in the control plots. Soil organic carbon was lost at a rate of 69.6±5.6 g m^?2 yr^?1 in the warmed plots and 22.5±2.7 g m^?2 yr^?1 in the control plots. Total nitrogen was lost at a rate of 4.6±0.4 g m^?2 yr^?1 in the warmed plots and 1.4±0.1 g m^?2 yr^?2 in the control plots. The amount of carbon and nitrogen loss caused by clipping is equivalent to or even larger than changes caused by global change factors such as warming and rising atmospheric CO₂ concentration. In addition, soil erosion rates were significantly correlated with clipping‐induced changes in soil moisture. Our results suggest that clipping for biofuel harvest results in significant soil erosion and accompanying losses of soil carbon and nitrogen, which is aggravated by warming.     

Long-term impact of a stand-replacing fire on ecosystem CO2 exchange of a ponderosa pine forest

Ponderosa pine (Pinus ponderosa) forests of the southwestern United States are a mosaic of stands where undisturbed forests are carbon sinks, and stands recovering from wildfires may be sources of carbon to the atmosphere for decades after the fire. However, the relative magnitude of these sinks and sources has never been directly measured in this region, limiting our understanding of the role of fire in regional and US carbon budgets. We used the eddy covariance technique to measure the CO₂ exchange of two forest sites, one burned by fire in 1996, and an unburned forest. The fire was a high‐intensity stand‐replacing burn that killed all trees. Ten years after the fire, the burned site was still a source of CO₂ to the atmosphere [109±6 (SEM) g C m^?2 yr^?1], whereas the unburned site was a sink (?164±23 g C m^?2 yr^?1). The fire reduced total carbon storage and shifted ecosystem carbon allocation from the forest floor and living biomass to necromass. Annual ecosystem respiration was lower at the burned site (480±5 g C m^?2 yr^?1) than at the unburned site (710±54 g C m^?2 yr^?1), but the difference in gross primary production was even larger (372±13 g C m^?2 yr^?1 at the burned site and 858±37 g C m^?2 yr^?1at the unburned site). Water availability controlled carbon flux in the warm season at both sites, and the burned site was a source of carbon in all months, even during the summer, when wet and warm conditions favored respiration more than photosynthesis. Our study shows that carbon losses following stand‐replacing fires in ponderosa pine forests can persist for decades due to slow recovery of the gross primary production. Because fire exclusion is becoming increasingly difficult in dry western forests, a large US forest carbon sink could shift to a decadal‐scale carbon source.     

Changes in soil organic carbon,nitrogen, pH and bulk density with the development of larch (Larix gmelinii) plantations in China

Under the government of China's environmental program known as Returning Farmland To Forests (RFTF), about 28 million hectares of farmland have been converted to tree plantation. This has led to a large accumulation of biomass carbon, but less is known about underground carbon‐related processes. One permanent plot (25 years of observation) and four chronosequence plot series comprising 159 plots of larch (Larix gmelinii) plantations in northeastern China were studied. Both methods found significant soil organic carbon (SOC) accumulation (96.4 g C m^?2 yr^?1) and bulk density decrease (5.7 mg cm^?3 yr^?1) in the surface soil layer (0–20 cm), but no consistent changes in deeper layers, indicating that larch planting under the RFTF program can increase SOC storage and improve the physical properties of surface soil. Nitrogen depletion (4.1–4.3 g m^?2 yr^?1), soil acidification (0.007–0.022 pH units yr^?1) and carbon/nitrogen (C/N) ratio increase (0.16–0.46 per year) were observed in lessive soil, whereas no significant changes were found in typical dark‐brown forest soil. This SOC accumulation rate (96.4 g m^?2 yr^?1) can take 39% of the total carbon sink capacity [net ecosystem exchange (NEE)] of larch forests in this region and the total soil carbon sequestration could be 87 Tg carbon within 20 years of plantation by approximating all larch plantations in northeastern China (4.5 Mha), showing the importance of soil carbon accumulation in the ecosystem carbon balance. By comparison with the rates of these processes in agricultural use, the RFTF program of reversing land use for agriculture will rehabilitate SOC, soil fertility and bulk density slowly (< 69% of the depletion rate in agricultural use), so that a much longer duration is needed to rehabilitate the underground function of soil via the RFTF program. Global forest plantations on abandoned farmland or function to protecting farmland are of steady growth and our findings may be important for understanding their underground carbon processes.     

ORGANIC MATTER DYNAMICS IN FOUR SEASONALLY FLOODED FOREST COMMUNITIES OF THE DISMAL SWAMP

Budgets of organic matter dynamics for plant communities of the Great Dismal Swamp were developed to summarize an extensive data base, determine patterns of biomass allocation, transfer and accumulation, and make comparisons with other forested wetlands. Aboveground net primary production on the flooded sites (1,050–1,176 g m^-2 yr^-1) was significantly greater than on a rarely flooded site (831 g m^-2 yr^-1). Estimates of belowground net primary production were comparable to aboveground production on flooded sites (824–1,221 gm^-2 yr^-1). However, productivity was nearly three times greater belowground than aboveground on the rarely flooded site (2,256 g m^-2 yr^-1). Aboveground productivity in Dismal Swamp forests is relatively high compared to other forested wetlands. This is attributed to the timing and periodic nature of flood events. Fine root turnover is shown to be an important source of soil organic matter. Estimates indicate that roots contribute about 60% of the annual increment to soil organic matter. Leaflitter contributes 6–28% and wood debris contributes 5–15%. Comparisons with other forested wetlands suggest that detritus accounts for greater than half of the total organic matter (living + dead) in many wetland systems.     

Fine root dynamics in a Norway spruce forest (Picea abies (L.) Karst) in eastern Sweden

The annual dynamics of live and dead fine roots for trees and the field layer species and live/dead ratios were investigated at a coniferous fern forest (Picea abies L. Karts) in Sweden. Our methods of estimating the average amount of fine roots involved the periodic sampling of fine roots in sequential cores on four sampling occasions. The highest live/dead ratio was found in the upper part of the humus layer for both tree and field-layer species and decreased with depth. Most tree fine roots on the four sampling occasions were found in the mineral soil horizon, where 86, 81, 85 and 89% of <1 mm and 89, 88, 89 and 92% of <2 mm diameter of the total amounts of live fine roots in the soil profile were found. The mean amounts of live fine roots of tree species for the total soil profile on the four sampling occasions was 317, 150, 139 and 248 g m^?2 for <1 mm and 410, 225, 224 and 351 g m^?2 for <2 mm diameter fine roots. The related amount of dead fine roots was 226, 321, 176 and 299 g m^?2 and 294, 424, 282 and 381 g m^?2, respectively. Average amounts of live and dead fine-roots and live/dead ratios from other Picea abies forest ecosystems were within the range of our estimates. The production of fine roots, <1 and <2 mm in diameter, estimated from the annual increments in live fine roots, was 207 and 303 g m^?2. The related accumulation of dead fine roots was 257 and 345 g m^?2, The turnover rate of tree fine roots <1 mm in diameter in the total soil profile amounted to 0.7 yr^?1 for live and 0.8 yr^?1 for dead fine roots. The related turnover rates for tree fine roots <2 mm were 0.4 yr^?1 and 0.7 yr^?1. Our data, although based on minimum estimates of the annual fluxes of live and dead fine roots, suggests a carbon flow to the forest soil from dead fine-roots even more substantial than from the needle litter fall. Fine-root data from several Picea abies forest ecosystems, suggest high turnover rates of both live and dead tree fine-roots.     

Changes in carbon storage and fluxes in a chronosequence of ponderosa pine

Forest development following stand‐replacing disturbance influences a variety of ecosystem processes including carbon exchange with the atmosphere. On a series of ponderosa pine (Pinius ponderosa var. Laws.) stands ranging from 9 to> 300 years in central Oregon, USA, we used biological measurements to estimate carbon storage in vegetation and soil pools, net primary productivity (NPP) and net ecosystem productivity (NEP) to examine variation with stand age. Measurements were made on plots representing four age classes with three replications: initiation (I, 9–23 years), young (Y, 56–89 years), mature (M, 95–106 years), and old (O, 190–316 years) stands typical of the forest type in the region. Net ecosystem productivity was lowest in the I stands (?124 g C m^?2 yr^?1), moderate in Y stands (118 g C m^?2 yr^?1), highest in M stands (170 g C m^?2 yr^?1), and low in the O stands (35 g C m^?2 yr^?1). Net primary productivity followed similar trends, but did not decline as much in the O stands. The ratio of fine root to foliage carbon was highest in the I stands, which is likely necessary for establishment in the semiarid environment, where forests are subject to drought during the growing season (300–800 mm precipitation per year). Carbon storage in live mass was the highest in the O stands (mean 17.6 kg C m^?2). Total ecosystem carbon storage and the fraction of ecosystem carbon in aboveground wood mass increased rapidly until 150–200 years, and did not decline in older stands. Forest inventory data on 950 ponderosa pine plots in Oregon show that the greatest proportion of plots exist in stands ～ 100 years old, indicating that a majority of stands are approaching maximum carbon storage and net carbon uptake. Our data suggests that NEP averages ～ 70 g C m^?2 year^?1 for ponderosa pine forests in Oregon. About 85% of the total carbon storage in biomass on the survey plots exists in stands greater than 100 years, which has implications for managing forests for carbon sequestration. To investigate variation in carbon storage and fluxes with disturbance, simulation with process models requires a dynamic parameterization for biomass allocation that depends on stand age, and should include a representation of competition between multiple plant functional types for space, water, and nutrients.     

Quantifying carbon sequestration as a result of soil erosion and deposition: retrospective assessment using caesium-137 and carbon inventories

The role of soil erosion in the global carbon cycle remains a contested subject. A new approach to the retrospective derivation of erosion‐induced quantitative fluxes of carbon between soil and atmosphere is presented and applied. The approach is based on the premise that soil redistribution perturbs the carbon cycle by driving disequilibrium between soil carbon content and input. This perturbation is examined by establishing the difference between measured carbon inventories and the inventories that would be found if input and content were in dynamic equilibrium. The carbon inventory of a profile in dynamic equilibrium is simulated by allowing lateral and vertical redistribution of carbon but treating all other profile inputs as equal to outputs. Caesium‐137 is used to derive rates of vertical and lateral soil redistribution. Both point and field‐scale estimates of carbon exchange with the atmosphere are derived using the approach for a field subject to mechanized agricultural in the United Kingdom. Sensitivity analysis is undertaken and demonstrates that the approach is robust. The results indicate that, despite a 15% decline in the carbon content of the cultivation layer of the eroded part of the field, this area has acted as a net sink of 11 ± 2 g C m^?2 yr^?1 over the last half century and that in the field as a whole, soil redistribution has driven a sink of 7 ± 2 g C m^?2 yr^?1 (6 ± 2 g C m^?2 yr^?1 if all eroded carbon transported beyond the field boundary is lost to the atmosphere) over the same period. This is the first empirical evidence for, and quantification of, dynamic replacement of eroded carbon. The relatively modest field‐scale net sink is more consistent with the identification of erosion and deposition as a carbon sink than a carbon source. There is a clear need to assemble larger databases with which to evaluate critically the carbon sequestration potential of erosion and deposition in a variety of conditions of agricultural management, climate, relief, and soil type. In any case, this study demonstrated that the operation of erosion and deposition processes within the boundaries of agricultural fields must be understood as a key driver of the net carbon cycle consequences of cultivating land.     

ROOT PRODUCTION IN FOUR COMMUNITIES IN THE GREAT DISMAL SWAMP

A sequential coring approach was used to measure root biomass and production over 1 year in four different communities within the Great Dismal Swamp. A second method, an implanted bag technique, was also used to measure root production, and values were generally lower using this technique. On all sites, fine roots were the most dynamic root component. Both biomass (1,887 g/m²) and production (354–989 g m ² yr^-1) were highest on the mixed hardwood site, the least flooded site, and second highest on the cedar site, the site with the longest duration of soil saturation (1,033 g/m² and 274–366 g m^-2 yr^-1). The maple-gum (696 g/m² and 59–91 g m^-2 yr^-1) and cypress (824 g/m² and 68–308 g m^-2 yr^-1) sites had similarly low amounts of biomass and rates of production. Environmental parameters that influenced production include frequency and duration of flooding, and soil type. Peaks in belowground production were observed on the most productive sites (mixed hardwood and cedar) in summer and late fall-winter; the other two sites exhibited little seasonal variability. The least flooded stand appears to allocate a greater percentage of net primary production belowground than the more extensively flooded stands. The ratio of above- and belowground allocation appears to change in response to a flooding gradient. This has major implications for ecosystem functions as carbon allocation patterns determine the array of litter types generated (leaves vs. roots) which affect decomposition rates and nutrient availability.     

Estimates of soil respiration and net primary production of three forests at different succession stages in South China

Soil respiration (heterotropic and autotropic respiration, R_g) and aboveground litter fall carbon were measured at three forests at different succession (early, middle and advanced) stages in Dinghushan Biosphere Reserve, Southern China. It was found that the soil respiration increases exponentially with soil temperature at 5 cm depth (T_s) according to the relation R_g=a exp(bT_s), and the more advanced forest community during succession has a higher value of a because of higher litter carbon input than the forests at early or middle succession stages. It was also found that the monthly soil respiration is linearly correlated with the aboveground litter carbon input of the previous month. Using measurements of aboveground litter and soil respiration, the net primary productions (NPPs) of three forests were estimated using nonlinear inversion. They are 475, 678 and 1148 g C m^?2 yr^?1 for the Masson pine forest (MPF), coniferous and broad‐leaf mixed forest (MF) and subtropical monsoon evergreen broad‐leaf forest (MEBF), respectively, in year 2003/2004, of which 54%, 37% and 62% are belowground NPP for those three respective forests if no change in live plant biomass is assumed. After taking account of the decrease in live plant biomass, we estimated the NPP of the subtropical MEBF is 970 g C m^?2 yr^?1 in year 2003/2004. Total amount of carbon allocated below ground for plant roots is 388 g C m^?2 yr^?1 for the MPF, 504 g C m^?2 yr^?1 for the coniferous and broad‐leaf MF and 1254 g C m^?2 yr^?1 for the subtropical MEBF in 2003/2004. Our results support the hypothesis that the amount of carbon allocation belowground increases during forest succession.     

Contemporary carbon accumulation in a boreal oligotrophic minerogenic mire – a significant sink after accounting for all C-fluxes

Based on theories of mire development and responses to a changing climate, the current role of mires as a net carbon sink has been questioned. A rigorous evaluation of the current net C-exchange in mires requires measurements of all relevant fluxes. Estimates of annual total carbon budgets in mires are still very limited. Here, we present a full carbon budget over 2 years for a boreal minerogenic oligotrophic mire in northern Sweden (64°11′N, 19°33′E). Data on the following fluxes were collected: land–atmosphere CO₂ exchange (continuous Eddy covariance measurements) and CH₄ exchange (static chambers during the snow free period); TOC (total organic carbon) in precipitation; loss of TOC, dissolved inorganic carbon (DIC) and CH₄ through stream water runoff (continuous discharge measurements and regular C-concentration measurements). The mire constituted a net sink of 27±3.4 (±SD) g C m⁻² yr⁻¹ during 2004 and 20±3.4 g C m⁻² yr⁻¹ during 2005. This could be partitioned into an annual surface–atmosphere CO₂ net uptake of 55±1.9 g C m⁻² yr⁻¹ during 2004 and 48±1.6 g C m⁻² yr⁻¹ during 2005. The annual NEE was further separated into a net uptake season, with an uptake of 92 g C m⁻² yr⁻¹ during 2004 and 86 g C m⁻² yr⁻¹ during 2005, and a net loss season with a loss of 37 g C m⁻² yr⁻¹ during 2004 and 38 g C m⁻² yr⁻¹ during 2005. Of the annual net CO₂-C uptake, 37% and 31% was lost through runoff (with runoff TOC>DIC≫CH₄) and 16% and 29% through methane emission during 2004 and 2005, respectively. This mire is still a significant C-sink, with carbon accumulation rates comparable to the long-term Holocene C-accumulation, and higher than the C-accumulation during the late Holocene in the region.     

不同放牧强度下短花针茅荒漠草原植被-土壤系统有机碳组分储量特征

草地生态系统作为陆地生态系统的重要组成部分,在全球碳循环中发挥着重要作用。以内蒙古短花针茅荒漠草原不同放牧强度样地为研究对象,通过分析地上植物、凋落物、根系、土壤中有机碳和土壤轻组有机碳,研究草原植被-土壤系统有机碳组分储量的变化特征,从碳储量角度为合理利用草原提供指导。研究结果表明:(1)不同放牧强度荒漠草原地上植物碳储量为11.98—44.51 g/m~2,凋落物碳储量10.43—36.12 g/m~2,根系(0—40cm)碳储量502.30—804.31 g/m~2,且对照区(CK)均显著高于中度放牧区(MG)、重度放牧区(HG);(2)0—40cm土壤碳储量为7817.43—9694.16 g/m~2,其中轻度放牧区(LG)碳储量为9694.16 g/m~2,显著高于CK、HG(P0.05);(3)植被—土壤系统的碳储量为8342.14—10494.80 g/m~2,LGMGCKHG,有机碳主要储存于土壤当中,占比约90.54%—93.71%,适度放牧利用有利于发挥草地生态系统的碳汇功能;(4)土壤轻组有机碳储量为484.20—654.62 g/m~2,LG储量最高,表明适度放牧有助于草原土壤营养物质的循环和积累。     

Soil carbon balance in a clonal Eucalyptus plantation in Congo: effects of logging on carbon inputs and soil CO2 efflux

Soil CO₂ efflux was measured in clear‐cut and intact plots in order to quantify the impact of harvest on soil respiration in an intensively managed Eucalyptus plantation, and to evaluate the increase in heterotrophic component of soil respiration because of the decomposition of harvest residues. Soil CO₂ effluxes showed a pronounced seasonal trend, which was well related to the pattern of precipitation and soil water content and were always significantly lower in the clear‐cut plots than in the intact plots. On an annual basis, soil respiration represented 1.57 and 0.91 kg_C m^?2 yr^?1 in intact and clear‐cut plots, respectively. During the first year following harvest, residues have lost 0.79 kg_C m^?2 yr^?1. Our estimate of heterotrophic respiration was calculated assuming that it was similar to soil respiration in the clear‐cut area except that the decomposition of residues did not occur, and it was further corrected for differences in soil water content between intact and clear‐cut plots and for the cessation of leaf and fine root turnover in clear cut. Heterotrophic respiration in clear‐cut plots was estimated at 1.18 kg_C m^?2 yr^?1 whereas it was only 0.65 kg_C m^?2 yr^?1 in intact plots (41% of soil respiration). Assumptions and uncertainties with these calculations are discussed.