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1.
Responses of soil respiration (CO2 emission) to simulated N deposition were studied in a disturbed (reforested forest with previous understory and litter harvesting) and a rehabilitated (reforested forest with no understory and litter harvesting) tropical forest in southern China from October 2005 to September 2006. The objectives of the study were to test the following hypotheses: (1) soil respiration is higher in rehabilitated forest than in disturbed forest; (2) soil respiration in both rehabilitated and disturbed tropical forests is stimulated by N additions; and (3) soil respiration is more sensitive to N addition in disturbed forest than in rehabilitated forest due to relatively low soil nutrient status in the former, resulting from different previous human disturbance. Static chamber and gas chromatography techniques were employed to quantify the soil respiration, following different N treatments (Control, no N addition; Low-N, 5 g N m−2 year−1; Medium-N, 10 g N m−2 year−1), which had been applied continuously for 26 months before the respiration measurement. Results showed that soil respiration exhibited a strong seasonal pattern, with the highest rates observed in the hot and wet growing season (April–September) and the lowest rates in winter (December–February) in both rehabilitated and disturbed forests. Soil respiration rates exhibited significant positive exponential relationship with soil temperature and significant positive linear relationship with soil moisture. Soil respiration was also significantly higher in the rehabilitated forest than in the disturbed forest. Annual mean soil respiration rate in the rehabilitated forest was 20% lower in low-N plots (71 ± 4 mg CO2-C m−2 h−1) and 10% lower in medium-N plots (80 ± 4 mg CO2-C m−2 h−1) than in the control plots (89 ± 5 mg CO2-C m−2 h−1), and the differences between the control and low-N or medium-N treatments were statistically significant. In disturbed forest, annual mean soil respiration rate was 5% lower in low-N plots (63 ± 3 mg CO2-C m−2 h−1) and 8% lower in medium-N plots (61 ± 3 mg CO2-C m−2 h−1) than in the control plots (66 ± 4 mg CO2-C m−2 h−1), but the differences among treatments were not significant. The depressed effects of experimental N deposition occurred mostly in the hot and wet growing season. Our results suggest that response of soil respiration to elevated N deposition in the reforested tropical forests may vary depending on the status of human disturbance. Responsible Editor: Hans Lambers.  相似文献   

2.
Fine root dynamics have the potential to contribute significantly to ecosystem‐scale biogeochemical cycling, including the production and emission of greenhouse gases. This is particularly true in tropical forests which are often characterized as having large fine root biomass and rapid rates of root production and decomposition. We examined patterns in fine root dynamics on two soil types in a lowland moist Amazonian forest, and determined the effect of root decay on rates of C and N trace gas fluxes. Root production averaged 229 (±35) and 153 (±27) g m?2 yr?1 for years 1 and 2 of the study, respectively, and did not vary significantly with soil texture. Root decay was sensitive to soil texture with faster rates in the clay soil (k=?0.96 year?1) than in the sandy loam soil (k=?0.61 year?1), leading to greater standing stocks of dead roots in the sandy loam. Rates of nitrous oxide (N2O) emissions were significantly greater in the clay soil (13±1 ng N cm?2 h?1) than in the sandy loam (1.4±0.2 ng N cm?2 h?1). Root mortality and decay following trenching doubled rates of N2O emissions in the clay and tripled them in sandy loam over a 1‐year period. Trenching also increased nitric oxide fluxes, which were greater in the sandy loam than in the clay. We used trenching (clay only) and a mass balance approach to estimate the root contribution to soil respiration. In clay soil root respiration was 264–380 g C m?2 yr?1, accounting for 24% to 35% of the total soil CO2 efflux. Estimates were similar using both approaches. In sandy loam, root respiration rates were slightly higher and more variable (521±206 g C m2 yr?1) and contributed 35% of the total soil respiration. Our results show that soil heterotrophs strongly dominate soil respiration in this forest, regardless of soil texture. Our results also suggest that fine root mortality and decomposition associated with disturbance and land‐use change can contribute significantly to increased rates of nitrogen trace gas emissions.  相似文献   

3.
Natural wetlands are critically important to global change because of their role in modulating atmospheric concentrations of CO2, CH4, and N2O. One 4‐year continuous observation was conducted to examine the exchanges of CH4 and N2O between three wetland ecosystems and the atmosphere as well as the ecosystem respiration in the Sanjiang Plain in Northeastern China. From 2002 to 2005, the mean annual budgets of CH4 and N2O, and ecosystem respiration were 39.40 ± 6.99 g C m?2 yr?1, 0.124 ± 0.05 g N m?2 yr?1, and 513.55 ± 8.58 g C m?2 yr?1 for permanently inundated wetland; 4.36 ± 1.79 g C m?2 yr?1, 0.11 ± 0.12 g N m?2 yr?1, and 880.50 ± 71.72 g C m?2 yr?1 for seasonally inundated wetland; and 0.21 ± 0.1 g C m?2 yr?1, 0.28 ± 0.11 g N m?2 yr?1, and 1212.83 ± 191.98 g C m?2 yr?1 for shrub swamp. The substantial interannual variation of gas fluxes was due to the significant climatic variability which underscores the importance of long‐term continuous observations. The apparent seasonal pattern of gas emissions associated with a significant relationship of gas fluxes to air temperature implied the potential effect of global warming on greenhouse gas emissions from natural wetlands. The budgets of CH4 and N2O fluxes and ecosystem respiration were highly variable among three wetland types, which suggest the uncertainties in previous studies in which all kinds of natural wetlands were treated as one or two functional types. New classification of global natural wetlands in more detailed level is highly expected.  相似文献   

4.
This study investigated how nitrogen (N) fertilization with 200 kg N ha?1 of urea affected ecosystem carbon (C) sequestration in the first‐postfertilization year in a Pacific Northwest Douglas‐fir (Pseudotsuga menziesii) stand on the basis of multiyear eddy‐covariance (EC) and soil‐chamber measurements before and after fertilization in combination with ecosystem modeling. The approach uses a data‐model fusion technique which encompasses both model parameter optimization and data assimilation and minimizes the effects of interannual climatic perturbations and focuses on the biotic and abiotic factors controlling seasonal C fluxes using a prefertilization 9‐year‐long time series of EC data (1998–2006). A process‐based ecosystem model was optimized using the half‐hourly data measured during 1998–2005, and the optimized model was validated using measurements made in 2006 and further applied to predict C fluxes for 2007 assuming the stand was not fertilized. The N fertilization effects on C sequestration were then obtained as differences between modeled (unfertilized stand) and EC or soil‐chamber measured (fertilized stand) C component fluxes. Results indicate that annual net ecosystem productivity in the first‐post‐N fertilization year increased by~83%, from 302 ± 19 to 552 ± 36 g m?2 yr?1, which resulted primarily from an increase in annual gross primary productivity of~8%, from 1938 ± 22 to 2095 ± 29 g m?2 yr?1 concurrent with a decrease in annual ecosystem respiration (Re) of~5.7%, from 1636 ± 17 to 1543 ± 31 g m?2 yr?1. Moreover, with respect to respiration, model results showed that the fertilizer‐induced reduction in Re (~93 g m?2 yr?1) principally resulted from the decrease in soil respiration Rs (~62 g m?2 yr?1).  相似文献   

5.
Rising atmospheric CO2 has been predicted to reduce litter decomposition as a result of CO2‐induced reductions in litter quality. However, available data have not supported this hypothesis in mesic ecosystems, and no data are available for desert or semi‐arid ecosystems, which account for more than 35% of the Earth's land area. The objective of our study was to explore controls on litter decomposition in the Mojave Desert using elevated CO2 and interannual climate variability as driving environmental factors. In particular, we sought to evaluate the extent to which decomposition is modulated by litter chemistry (C:N) and litter species and tissue composition. Naturally senesced litter was collected from each of nine 25 m diameter experimental plots, with six plots exposed to ambient [CO2] or 367 μL CO2 L?1 and three plots continuously fumigated with elevated [CO2] (550 μL CO2 L?1) using FACE technology beginning in April 1997. All litter collected in 1998 (a wet, or El Niño year; 306 mm precipitation) was pooled as was litter collected in 1999 (a dry year; 94 mm). Samples were allowed to decompose for 4 and 12 months starting in May 2001 in mesh litterbags in the locations from which litter was collected. Decomposition of litter produced under elevated CO2 and ambient CO2 did not differ. Litter produced in the wetter year showed more rapid initial decomposition (over the first 4 months) than that produced in the drier year (27±2% yr?1 or 7.8±0.7 g m?2 yr?1 for 1998 litter; 18±3% yr?1 or 2.2±0.4 g m?2 yr?1 for 1999 litter). C:N ratios of litter produced under elevated CO2 (wet year: 37±0.5; dry year: 42±2.5) were higher than those of litter produced under ambient CO2 (wet year: 34±1.1; dry year: 35±1.4). Litter production in the wet year (amb. CO2: 25.1±1.1 g m?2 yr?1; elev. CO2: 35.0±1.1 g m?2 yr?1) was more than twice as high as that in the dry year (amb. CO2: 11.6±1.7 g m?2, elev. CO2: 13.3±3.4 g m?2), and contained a greater proportion of Lycium pallidum and a lower proportion of Larrea tridentata than litter produced in the dry year. Decomposition, viewed across all treatments, decreased with increasing C:N ratios, decreased with increasing proportions of Larrea tridentata and increased with increasing proportions of Lycium pallidum and Lycium andersonii. Because litter C:N did not vary by litter production year, and CO2 did not alter decomposition or litter species/tissue composition, it is likely that the impact of year‐to‐year variation in precipitation on the proportion of key plant species in the litter may be the most important way in which litter decomposition will be modulated in the Mojave Desert under future rising atmospheric CO2.  相似文献   

6.
Wetlands can influence global climate via greenhouse gas (GHG) exchange of carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O). Few studies have quantified the full GHG budget of wetlands due to the high spatial and temporal variability of fluxes. We report annual open‐water diffusion and ebullition fluxes of CO2, CH4, and N2O from a restored emergent marsh ecosystem. We combined these data with concurrent eddy‐covariance measurements of whole‐ecosystem CO2 and CH4 exchange to estimate GHG fluxes and associated radiative forcing effects for the whole wetland, and separately for open‐water and vegetated cover types. Annual open‐water CO2, CH4, and N2O emissions were 915 ± 95 g C‐CO2 m?2 yr?1, 2.9 ± 0.5 g C‐CH4 m?2 yr?1, and 62 ± 17 mg N‐N2O m?2 yr?1, respectively. Diffusion dominated open‐water GHG transport, accounting for >99% of CO2 and N2O emissions, and ~71% of CH4 emissions. Seasonality was minor for CO2 emissions, whereas CH4 and N2O fluxes displayed strong and asynchronous seasonal dynamics. Notably, the overall radiative forcing of open‐water fluxes (3.5 ± 0.3 kg CO2‐eq m?2 yr?1) exceeded that of vegetated zones (1.4 ± 0.4 kg CO2‐eq m?2 yr?1) due to high ecosystem respiration. After scaling results to the entire wetland using object‐based cover classification of remote sensing imagery, net uptake of CO2 (?1.4 ± 0.6 kt CO2‐eq yr?1) did not offset CH4 emission (3.7 ± 0.03 kt CO2‐eq yr?1), producing an overall positive radiative forcing effect of 2.4 ± 0.3 kt CO2‐eq yr?1. These results demonstrate clear effects of seasonality, spatial structure, and transport pathway on the magnitude and composition of wetland GHG emissions, and the efficacy of multiscale flux measurement to overcome challenges of wetland heterogeneity.  相似文献   

7.
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 kgC m?2 yr?1 in intact and clear‐cut plots, respectively. During the first year following harvest, residues have lost 0.79 kgC 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 kgC m?2 yr?1 whereas it was only 0.65 kgC m?2 yr?1 in intact plots (41% of soil respiration). Assumptions and uncertainties with these calculations are discussed.  相似文献   

8.
Carbon exchange of grazed pasture on a drained peat soil   总被引:1,自引:0,他引:1  
Land‐use changes have contributed to increased atmospheric CO2 concentrations. Conversion from natural peatlands to agricultural land has led to widespread subsidence of the peat surface caused by soil compaction and mineralization. To study the net ecosystem exchange of carbon (C) and the contribution of respiration to peat subsidence, eddy covariance measurements were made over pasture on a well‐developed, drained peat soil from 22 May 2002 to 21 May 2003. The depth to the water table fluctuated between 0.02 m in winter 2002 to 0.75 m during late summer and early autumn 2003. Peat soil moisture content varied between 0.6 and 0.7 m3 m?3 until the water table dropped below 0.5 m, when moisture content reached 0.38 m3 m?3. Neither depth to water table nor soil moisture was found to have an effect on the rate of night‐time respiration (ranging from 0.4–8.0 μmol CO2 m?2 s?1 in winter and summer, respectively). Most of the variance in night‐time respiration was explained by changes in the 0.1 m soil temperature (r2=0.93). The highest values for daytime net ecosystem exchange were measured in September 2002, with a maximum of ?17.2 μmol CO2 m?2 s?1. Grazing events and soil moisture deficiencies during a short period in summer reduced net CO2 exchange. To establish an annual C balance for this ecosystem, non‐linear regression was used to model missing data. Annually integrated (CO2) C exchange for this peat–pasture ecosystem was 45±500 kg C ha?1 yr?1. After including other C exchanges (methane emissions from cows and production of milk), the net annual C loss was 1061±500 kg C ha?1 yr?1.  相似文献   

9.
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.  相似文献   

10.
Freshwater marshes are well‐known for their ecological functions in carbon sequestration, but complete carbon budgets that include both methane (CH4) and lateral carbon fluxes for these ecosystems are rarely available. To the best of our knowledge, this is the first full carbon balance for a freshwater marsh where vertical gaseous [carbon dioxide (CO2) and CH4] and lateral hydrologic fluxes (dissolved and particulate organic carbon) have been simultaneously measured for multiple years (2011–2013). Carbon accumulation in the sediments suggested that the marsh was a long‐term carbon sink and accumulated ~96.9 ± 10.3 (±95% CI) g C m?2 yr?1 during the last ~50 years. However, abnormal climate conditions in the last 3 years turned the marsh to a source of carbon (42.7 ± 23.4 g C m?2 yr?1). Gross ecosystem production and ecosystem respiration were the two largest fluxes in the annual carbon budget. Yet, these two fluxes compensated each other to a large extent and led to the marsh being a CO2 sink in 2011 (?78.8 ± 33.6 g C m?2 yr?1), near CO2‐neutral in 2012 (29.7 ± 37.2 g C m?2 yr?1), and a CO2 source in 2013 (92.9 ± 28.0 g C m?2 yr?1). The CH4 emission was consistently high with a three‐year average of 50.8 ± 1.0 g C m?2 yr?1. Considerable hydrologic carbon flowed laterally both into and out of the marsh (108.3 ± 5.4 and 86.2 ± 10.5 g C m?2 yr?1, respectively). In total, hydrologic carbon fluxes contributed ~23 ± 13 g C m?2 yr?1 to the three‐year carbon budget. Our findings highlight the importance of lateral hydrologic inflows/outflows in wetland carbon budgets, especially in those characterized by a flow‐through hydrologic regime. In addition, different carbon fluxes responded unequally to climate variability/anomalies and, thus, the total carbon budgets may vary drastically among years.  相似文献   

11.
Nitrogen (N) deposition is a component of global change that has considerable impact on belowground carbon (C) dynamics. Plant growth stimulation and alterations of fungal community composition and functions are the main mechanisms driving soil C gains following N deposition in N‐limited temperate forests. In N‐rich tropical forests, however, N deposition generally has minor effects on plant growth; consequently, C storage in soil may strongly depend on the microbial processes that drive litter and soil organic matter decomposition. Here, we investigated how microbial functions in old‐growth tropical forest soil responded to 13 years of N addition at four rates: 0 (Control), 50 (Low‐N), 100 (Medium‐N), and 150 (High‐N) kg N ha?1 year?1. Soil organic carbon (SOC) content increased under High‐N, corresponding to a 33% decrease in CO2 efflux, and reductions in relative abundances of bacteria as well as genes responsible for cellulose and chitin degradation. A 113% increase in N2O emission was positively correlated with soil acidification and an increase in the relative abundances of denitrification genes (narG and norB). Soil acidification induced by N addition decreased available P concentrations, and was associated with reductions in the relative abundance of phytase. The decreased relative abundance of bacteria and key functional gene groups for C degradation were related to slower SOC decomposition, indicating the key mechanisms driving SOC accumulation in the tropical forest soil subjected to High‐N addition. However, changes in microbial functional groups associated with N and P cycling led to coincidentally large increases in N2O emissions, and exacerbated soil P deficiency. These two factors partially offset the perceived beneficial effects of N addition on SOC storage in tropical forest soils. These findings suggest a potential to incorporate microbial community and functions into Earth system models considering their effects on greenhouse gas emission, biogeochemical processes, and biodiversity of tropical ecosystems.  相似文献   

12.
We present the annual patterns of net ecosystem‐atmosphere exchange (NEE) of CO2 and H2O observed from a 447 m tall tower sited within a mixed forest in northern Wisconsin, USA. The methodology for determining NEE from eddy‐covariance flux measurements at 30, 122 and 396 m above the ground, and from CO2 mixing ratio measurements at 11, 30, 76, 122, 244 and 396 m is described. The annual cycle of CO2 mixing ratio in the atmospheric boundary layer (ABL) is also discussed, and the influences of local NEE and large‐scale advection are estimated. During 1997 gross ecosystem productivity (947?18 g C m?2 yr?1), approximately balanced total ecosystem respiration (963±19 g C m?2 yr?1), and NEE of CO2 was close to zero (16±19 g C m?2 yr?1 emitted into the atmosphere). The error bars represent the standard error of the cumulative daily NEE values. Systematic errors are also assessed. The identified systematic uncertainties in NEE of CO2 are less than 60 g C m?2 yr?1. The seasonal pattern of NEE of CO2 was highly correlated with leaf‐out and leaf‐fall, and soil thaw and freeze, and was similar to purely deciduous forest sites. The mean daily NEE of CO2 during the growing season (June through August) was ?1.3 g C m?2 day?1, smaller than has been reported for other deciduous forest sites. NEE of water vapor largely followed the seasonal pattern of NEE of CO2, with a lag in the spring when water vapor fluxes increased before CO2 uptake. In general, the Bowen ratios were high during the dormant seasons and low during the growing season. Evapotranspiration normalized by potential evapotranspiration showed the opposite pattern. The seasonal course of the CO2 mixing ratio in the ABL at the tower led the seasonal pattern of NEE of CO2 in time: in spring, CO2 mixing ratios began to decrease prior to the onset of daily net uptake of CO2 by the forest, and in fall mixing ratios began to increase before the forest became a net source for CO2 to the atmosphere. Transport as well as local NEE of CO2 are shown to be important components of the ABL CO2 budget at all times of the year.  相似文献   

13.
Chronic N additions to forest ecosystems can enhance soil N availability, potentially leading to reduced C allocation to root systems. This in turn could decrease soil CO2 efflux. We measured soil respiration during the first, fifth, sixth and eighth years of simulated atmospheric NO3? deposition (3 g N m?2 yr?1) to four sugar maple‐dominated northern hardwood forests in Michigan to assess these possibilities. During the first year, soil respiration rates were slightly, but not significantly, higher in the NO3?‐amended plots. In all subsequent measurement years, soil respiration rates from NO3?‐amended soils were significantly depressed. Soil temperature and soil matric potential were measured concurrently with soil respiration and used to develop regression relationships for predicting soil respiration rates. Estimates of growing season and annual soil CO2 efflux made using these relationships indicate that these C fluxes were depressed by 15% in the eighth year of chronic NO3? additions. The decrease in soil respiration was not due to reduced C allocation to roots, as root respiration rates, root biomass, and root turnover were not significantly affected by N additions. Aboveground litter also was unchanged by the 8 years of treatment. Of the remaining potential causes for the decline in soil CO2 efflux, reduced microbial respiration appears to be the most likely possibility. Documented reductions in microbial biomass and the activities of extracellular enzymes used for litter degradation on the NO3?‐amended plots are consistent with this explanation.  相似文献   

14.
Urban ecosystems are expanding globally, and assessing the ecological consequences of urbanization is critical to understanding the biology of local and global change related to land use. We measured carbon (C) fluxes, nitrogen (N) cycling, and soil microbial community structure in a replicated (n=3) field experiment comparing urban lawns to corn, wheat–fallow, and unmanaged shortgrass steppe ecosystems in northern Colorado. The urban and corn sites were irrigated and fertilized. Wheat and shortgrass steppe sites were not fertilized or irrigated. Aboveground net primary productivity (ANPP) in urban ecosystems (383±11 C m?2 yr?1) was four to five times greater than wheat or shortgrass steppe but significantly less than corn (537±44 C m?2 yr?1). Soil respiration (2777±273 g C m?2 yr?1) and total belowground C allocation (2602±269 g C m?2 yr?1) in urban ecosystems were both 2.5 to five times greater than any other land‐use type. We estimate that for a large (1578 km2) portion of Larimer County, Colorado, urban lawns occupying 6.4% of the land area account for up to 30% of regional ANPP and 24% of regional soil respiration from land‐use types that we sampled. The rate of N cycling from urban lawn mower clippings to the soil surface was comparable with the rate of N export in harvested corn (both ~12–15 g N m?2 yr?1). A one‐time measurement of microbial community structure via phospholipid fatty acid analysis suggested that land‐use type had a large impact on microbial biomass and a small impact on the relative abundance of broad taxonomic groups of microorganisms. Our data are consistent with several other studies suggesting that urbanization of arid and semiarid ecosystems leads to enhanced C cycling rates that alter regional C budgets.  相似文献   

15.
The magnitude, temporal, and spatial patterns of soil‐atmospheric greenhouse gas (hereafter referred to as GHG) exchanges in forests near the Tropic of Cancer are still highly uncertain. To contribute towards an improvement of actual estimates, soil‐atmospheric CO2, CH4, and N2O fluxes were measured in three successional subtropical forests at the Dinghushan Nature Reserve (hereafter referred to as DNR) in southern China. Soils in DNR forests behaved as N2O sources and CH4 sinks. Annual mean CO2, N2O, and CH4 fluxes (mean±SD) were 7.7±4.6 Mg CO2‐C ha?1 yr?1, 3.2±1.2 kg N2O‐N ha?1 yr?1, and 3.4±0.9 kg CH4‐C ha?1 yr?1, respectively. The climate was warm and wet from April through September 2003 (the hot‐humid season) and became cool and dry from October 2003 through March 2004 (the cool‐dry season). The seasonality of soil CO2 emission coincided with the seasonal climate pattern, with high CO2 emission rates in the hot‐humid season and low rates in the cool‐dry season. In contrast, seasonal patterns of CH4 and N2O fluxes were not clear, although higher CH4 uptake rates were often observed in the cool‐dry season and higher N2O emission rates were often observed in the hot‐humid season. GHG fluxes measured at these three sites showed a clear increasing trend with the progressive succession. If this trend is representative at the regional scale, CO2 and N2O emissions and CH4 uptake in southern China may increase in the future in light of the projected change in forest age structure. Removal of surface litter reduced soil CO2 effluxes by 17–44% in the three forests but had no significant effect on CH4 absorption and N2O emission rates. This suggests that microbial CH4 uptake and N2O production was mainly related to the mineral soil rather than in the surface litter layer.  相似文献   

16.
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.  相似文献   

17.
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.  相似文献   

18.
Response of plant biodiversity to increased availability of nitrogen (N) has been investigated in temperate and boreal forests, which are typically N‐limited, but little is known in tropical forests. We examined the effects of artificial N additions on plant diversity (species richness, density and cover) of the understory layer in an N saturated old‐growth tropical forest in southern China to test the following hypothesis: N additions decrease plant diversity in N saturated tropical forests primarily from N‐mediated changes in soil properties. Experimental additions of N were administered at the following levels from July 2003 to July 2008: no addition (Control); 50 kg N ha?1 yr?1 (Low‐N); 100 kg N ha?1 yr?1 (Medium‐N), and 150 kg N ha?1 yr?1 (High‐N). Results showed that no understory species exhibited positive growth response to any level of N addition during the study period. Although low‐to‐medium levels of N addition (≤100 kg N ha?1 yr?1) generally did not alter plant diversity through time, high levels of N addition significantly reduced species diversity. This decrease was most closely related to declines within tree seedling and fern functional groups, as well as to significant increases in soil acidity and Al mobility, and decreases in Ca availability and fine‐root biomass. This mechanism for loss of biodiversity provides sharp contrast to competition‐based mechanisms suggested in studies of understory communities in other forests. Our results suggest that high‐N additions can decrease plant diversity in tropical forests, but that this response may vary with rate of N addition.  相似文献   

19.
Soil respiration is derived from heterotrophic (decomposition of soil organic matter) and autotrophic (root/rhizosphere respiration) sources, but there is considerable uncertainty about what factors control variations in their relative contributions in space and time. We took advantage of a unique whole‐ecosystem radiocarbon label in a temperate forest to partition soil respiration into three sources: (1) recently photosynthesized carbon (C), which dominates root and rhizosphere respiration; (2) leaf litter decomposition and (3) decomposition of root litter and soil organic matter >1–2 years old. Heterotrophic sources and specifically leaf litter decomposition were large contributors to total soil respiration during the growing season. Relative contributions from leaf litter decomposition ranged from a low of ~1±3% of total soil respiration (6± 3 mg C m?2 h?1) when leaf litter was extremely dry, to a high of 42±16% (96± 38 mg C m?2 h?1). Total soil respiration fluxes varied with the strength of the leaf litter decomposition source, indicating that moisture‐dependent changes in litter decomposition drive variability in total soil respiration fluxes. In the surface mineral soil layer, decomposition of C fixed in the original labeling event (3–5 years earlier) dominated the isotopic signature of heterotrophic respiration. Root/rhizosphere respiration accounted for 16±10% to 64±22% of total soil respiration, with highest relative contributions coinciding with low overall soil respiration fluxes. In contrast to leaf litter decomposition, root respiration fluxes did not exhibit marked temporal variation ranging from 34±14 to 40±16 mg C m?2 h?1 at different times in the growing season with a single exception (88±35 mg C m?2 h?1). Radiocarbon signatures of root respired CO2 changed markedly between early and late spring (March vs. May), suggesting a switch from stored nonstructural carbohydrate sources to more recent photosynthetic products.  相似文献   

20.
Carbon dioxide exchange, soil C and N, leaf mineral nutrition and leaf carbon isotope discrimination (LCID‐Δ) were measured in three High Arctic tundra ecosystems over 2 years under ambient and long‐term (9 years) warmed (~2°C) conditions. These ecosystems are located at Alexandra Fiord (79°N) on Ellesmere Island, Nunavut, and span a soil water gradient; dry, mesic, and wet tundra. Growing season CO2 fluxes (i.e., net ecosystem exchange (NEE), gross ecosystem photosynthesis (GEP), and ecosystem respiration (Re)) were measured using an infrared gas analyzer and winter C losses were estimated by chemical absorption. All three tundra ecosystems lost CO2 to the atmosphere during the winter, ranging from 7 to 12 g CO2‐C m?2 season?1 being highest in the wet tundra. The period during the growing season when mesic tundra switch from being a CO2 source to a CO2 sink was increased by 2 weeks because of warming and increases in GEP. Warming during the summer stimulated dry tundra GEP more than Re and thus, NEE was consistently greater under warmed as opposed to ambient temperatures. In mesic tundra, warming stimulated GEP with no effect on Re increasing NEE by ~10%, especially in the first half of the summer. During the ~70 days growing season (mid‐June–mid‐August), the dry and wet tundra ecosystems were net CO2‐C sinks (30 and 67 g C m?2 season?1, respectively) and the mesic ecosystem was a net C source (58 g C m?2 season?1) to the atmosphere under ambient temperature conditions, due in part to unusual glacier melt water flooding that occurred in the mesic tundra. Experimental warming during the growing season increased net C uptake by ~12% in dry tundra, but reduced net C uptake by ~20% in wet tundra primarily because of greater rates of Re as opposed to lower rates of GEP. Mesic tundra responded to long‐term warming with ~30% increase in GEP with almost no change in Re reducing this tundra type to a slight C source (17 g C m?2 season?1). Warming caused LCID of Dryas integrafolia plants to be higher in dry tundra and lower in Salix arctic plants in mesic and wet tundra. Our findings indicate that: (1) High Arctic ecosystems, which occur in similar mesoclimates, have different net CO2 exchange rates with the atmosphere; (2) long‐term warming can increase the net CO2 exchange of High Arctic tundra by stimulating GEP, but it can also reduce net CO2 exchange in some tundra types during the summer by stimulating Re to a greater degree than stimulating GEP; (3) after 9 years of experimental warming, increases in soil carbon and nitrogen are detectable, in part, because of increases in deciduous shrub cover, biomass, and leaf litter inputs; (4) dry tundra increases in GEP, in response to long‐term warming, is reflected in D. integrifolia LCID; and (5) the differential carbon exchange responses of dry, mesic, and wet tundra to similar warming magnitudes appear to depend, in part, on the hydrologic (soil water) conditions. Annual net ecosystem CO2‐C exchange rates ranged from losses of 64 g C m?2 yr?1 to gains of 55 g C m?2 yr?1. These magnitudes of positive NEE are close to the estimates of NPP for these tundra types in Alexandra Fiord and in other High Arctic locations based on destructive harvests.  相似文献   

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