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1.
This paper reports the results of soil respiration (SR, including heterotrophic and autotrophic respiration), in a presumably successional series (early, middle and advanced) of subtropical forests in Dinghushan Biosphere Reserve in Guangdong Province, China. A static chamber method was used to characterize SR in dynamics of diurnal and seasonal patterns. The relationships of SR with soil temperature (ST) at 5 cm depth and with soil moisture (SM) at 0-10 cm depth were studied in order to estimate the annual SR of each of the forests. The annual SR in a climax forest community, monsoon evergreen broad-leaved forest (MEBF) was estimated as 1163.0 g C m−2 year−1 and in its successional communities, coniferous and broad-leaved mixed forest (MF) and the Masson pine forest (MPF) were 592.1 g C m−2 year−1, 1023.7 g C m−2 year−1, respectively. In addition, removal of surface litter led to the reduction of annual SR by 27-45% in those three forests. Analysis of the results indicated that the annual SR was highly correlated with both ST and SM. Furthermore, ST and SM themselves were highly correlated with each other across season in this study area. Thus for seasonal predictive SR model, either ST or SM could be integrated. However, for SR daily change prediction, both ST and SM were required because of confounding effects of ST and SM on a diurnal time scale. The Q10 values of SR derived from ST dependence function were 2.37, 2.31 and 2.25 in the three forests: MPF, MF and MEBF, respectively, suggesting a decreasing trend of the Q10 with the degree of forest succession.  相似文献   

2.
Distinguishing between root and non-root derived CO2 efflux is important when determining rates of soil organic matter turnover, however, in practice they remain difficult to separate. Our aim was to evaluate two methods for determining the component of below-ground respiration not dependent on plant roots (i.e., basal soil respiration; Rb). The first approach estimated Rb indirectly from the y-intercept of linear regressions between below-ground respiration (BGR) and root biomass. The second approach involved direct measurements of soil respiration from bare plots. To compare the contrasting approaches, BGR and crop biomass measurements were collected throughout the year in a range of agricultural systems. We found that both methods were very closely correlated with each other. Values of Rb determined by the intercept approach, however, were slightly higher than those determined by measurement of bare plots. Both approaches showed a seasonal trend with estimates of Rb lowest in winter months at 0.02 t C ha−1 month−1 for the y-intercept approach and 0.11 t C ha−1 month−1 for the bare plots approach, even after the data had been corrected for the influence of soil temperature. Highest rates of Rb occurred from the height to the end of the crop growing season (0.8-1.5 t C ha−1 month−1). The annual CO2 efflux due to Rb was estimated to be 8.1 t C ha−1 y−1 from the y-intercept approach and 6.8 t C ha−1 y−1 from bare plots. Annual BGR was 12.1 t C ha−1 y−1. We conclude that both methods provide similar estimates of Rb, however, logistically the bare plots approach is much easier to undertake than the y-intercept approach.  相似文献   

3.
Nitrogen (N) deposition to semiarid ecosystems is increasing globally, yet few studies have investigated the ecological consequences of N enrichment in these ecosystems. Furthermore, soil CO2 flux – including plant root and microbial respiration – is a key feedback to ecosystem carbon (C) cycling that links ecosystem processes to climate, yet few studies have investigated the effects of N enrichment on belowground processes in water-limited ecosystems. In this study, we conducted two-level N addition experiments to investigate the effects of N enrichment on microbial and root respiration in a grassland ecosystem on the Loess Plateau in northwestern China. Two years of high N additions (9.2 g N m−2 y−1) significantly increased soil CO2 flux, including both microbial and root respiration, particularly during the warm growing season. Low N additions (2.3 g N m−2 y−1) increased microbial respiration during the growing season only, but had no significant effects on root respiration. The annual temperature coefficients (Q10) of soil respiration and microbial respiration ranged from 1.86 to 3.00 and 1.86 to 2.72 respectively, and there was a significant decrease in Q10 between the control and the N treatments during the non-growing season but no difference was found during the growing season. Following nitrogen additions, elevated rates of root respiration were significantly and positively related to root N concentrations and biomass, while elevated rates of microbial respiration were related to soil microbial biomass C (SMBC). The microbial respiration tended to respond more sensitively to N addition, while the root respiration did not have similar response. The different mechanisms of N addition impacts on soil respiration and its components and their sensitivity to temperature identified in this study may facilitate the simulation and prediction of C cycling and storage in semiarid grasslands under future scenarios of global change.  相似文献   

4.
Quantifying global patterns of forest soil respiration (SR), its components of heterotrophic respiration (HR) and belowground autotrophic respiration (AR), and their responses to temperature and precipitation are vital to accurately evaluate responses of the terrestrial carbon balance to future climate change. There is great uncertainty associated with responses of SR to climate change, concerning the differences in climatic controls and apparent Q10 (the factor by which respiration increases for a 10 °C increase in temperature) over HR and AR. Here, we examine available information on SR, HR, AR, the contribution of HR to SR (HR/SR), and Q10 of SR and its components from a diverse global database of forest ecosystems. The goals were to test how SR and its two components (AR and HR) respond to temperature and precipitation changes, and to test the differences in apparent Q10 between AR and HR. SR increased linearly with mean annual temperature (MAT), but responded non-linearly to mean annual precipitation (MAP) in naturally-regenerated forests. For every 1 °C increase in MAT, overall emissions from SR increased by 24.6 g C m−2 yr−1. When MAP was less than 813 mm, every 100 mm increase in MAP led to a release of 75.3 g C m−2 yr−1, but the increase rate declined to 20.3 g C m−2 yr−1 when MAP was greater than 813 mm. MAT explained less variation in AR than that in HR. The overall emissions in AR and HR for every 1 °C increase in MAT, increased by 12.9 and 16.1 g C m−2 yr−1, respectively. The AR emissions for every 100 mm increase in MAP, increased by 44.5 g C m−2 yr−1 when MAP less than 1000 mm. However, above the threshold, AR emissions stayed relatively constant. HR increased linearly by 15.0 g C m−2 yr−1 with every 100 mm increased in MAP. The Q10 value of SR increased with increasing depth at which soil temperature was measured up to 10 cm and was negatively correlated with HR/SR. Our synthesis suggests AR and HR differ in their responses to temperature and precipitation change. We also emphasized the importance of information on soil temperature measurement depth when applying field estimation of Q10 values into current terrestrial ecosystem models. Q10 values derived from field SR measurements including AR, will likely overestimate the temperature response of HR on a future warmer earth.  相似文献   

5.
Most soil respiration measurements are conducted during the growing season. In tundra and boreal forest ecosystems, cumulative winter soil CO2 fluxes are reported to be a significant component of their annual carbon budgets. However, little information on winter soil CO2 efflux is known from mid-latitude ecosystems. Therefore, comparing measurements of soil respiration taken annually versus during the growing season will improve the accuracy of ecosystem carbon budgets and the response of soil CO2 efflux to climate changes. In this study we measured winter soil CO2 efflux and its contribution to annual soil respiration for seven ecosystems (three forests: Pinus sylvestris var. mongolica plantation, Larix principis-rupprechtii plantation and Betula platyphylla forest; two shrubs: Rosa bella and Malus baccata; and two meadow grasslands) in a forest-steppe ecotone, north China. Overall mean winter and growing season soil CO2 effluxes were 0.15-0.26 μmol m−2 s−1 and 2.65-4.61 μmol m−2 s−1, respectively, with significant differences in the growing season among the different ecosystems. Annual Q10 (increased soil respiration rate per 10 °C increase in temperature) was generally higher than the growing season Q10. Soil water content accounted for 84% of the variations in growing season Q10 and soil temperature range explained 88% of the variation in annual Q10. Soil organic carbon density to 30 cm depth was a good surrogate for SR10 (basal soil respiration at a reference temperature of 10 °C). Annual soil CO2 efflux ranged from 394.76 g C m−2 to 973.18 g C m−2 using observed ecosystem-specific response equations between soil respiration and soil temperature. Estimates ranged from 424.90 g C m−2 to 784.73 g C m−2 by interpolating measured soil respiration between sampling dates for every day of the year and then computing the sum to obtain the annual value. The contributions of winter soil CO2 efflux to annual soil respiration were 3.48-7.30% and 4.92-7.83% using interpolated and modeled methods, respectively. Our results indicate that in mid-latitude ecosystems, soil CO2 efflux continues throughout the winter and winter soil respiration is an important component of annual CO2 efflux.  相似文献   

6.
Forests play a significant role in the global carbon (C) cycle. Variability in weather, species, stand age, and current and past disturbances are some of the factors that control stand-level C dynamics. This study examines the relative roles of stand age and associated structural characteristics and weather variability on the exchange of carbon dioxide between the atmosphere and three different coastal Douglas-fir stands at different stages of development after clearcut harvesting. The eddy covariance technique was used to measure carbon dioxide fluxes and a portable soil chamber system was used to measure soil respiration in the three stands located within 50 km of each other on the east coast of Vancouver Island, British Columbia, Canada. In 2002, the recently clearcut harvested stand (HDF00) was a large C source, the pole/sapling aged stand (HDF88) was a moderate C source, and the rotation-aged stand (DF49) was a moderate C sink (net ecosystem production of −606, −133, and 254 g C m−2 year−1, respectively). Annual gross ecosystem production and ecosystem respiration also increased with increasing stand age. Differences in stand structural characteristics such as species composition and phenology were important in determining the timing and magnitude of maximum gross ecosystem production and net ecosystem production through the year. Both soil and ecosystem respiration were exponentially related to soil temperature in each stand with total ecosystem respiration differing more among stands than soil respiration. Between 1998 and 2003, annual net ecosystem production ranged from 254 to 424 g C m−2 year−1 over 6 years for DF49, from −623 to −564 g C m−2 year−1 over 3 years for HDF00, and from −154 to −133 g C m−2 year−1 over 2 years for HDF88. Interannual variations in C exchange of the oldest, most structurally stable stand (DF49) were related to variations in spring weather while the rapid growth of understory and pioneer species influenced variations in HDF00. The differences in net ecosystem production among stands (maximum of 1000 g C m−2 year−1 between the oldest and youngest stands) were an order of magnitude greater than the differences among years within a stand and emphasized the importance of age-related differences in stand structure on C exchange processes.  相似文献   

7.
Peatlands cover about 21% of the landscape and contain about 80% of the soil carbon stock in western Canada. However, the current rates of carbon accumulation and the environmental controls on ecosystem photosynthesis and respiration in peatland ecosystems are poorly understood. As part of Fluxnet-Canada, we continuously measured net ecosystem carbon dioxide exchange (NEE) using the eddy covariance technique in a treed fen dominated by stunted Picea mariana and Larix laricina trees during August 2003–December 2004. The total carbon stock in the ecosystem was approximately 51,000 g C m−2, with only 540 g C m−2 contributed by live above ground vegetation. The NEE measurements were used to parameterize simple physiological models to assess temporal variation in maximum ecosystem photosynthesis (Amax) and ecosystem respiration rate at 10 °C (R10). During mid-summer the ecosystem had a relatively high Amax (approx. 30 μmol m−2 s−1) with relatively low R10 (approx. 4 μmol m−2 s−1). The peak mid-day NEE uptake rate during July and August was 10 μmol m−2 s−1. The ecosystem showed large seasonal variation in photosynthetic and respiratory activity that was correlated with shifts in temperature, with both spring increases and fall decreases in Amax well predicted by the mean daily air temperature averaged over the preceding 21 days. Leaf-level gas exchange and spectral reflectance measurements also suggested that seasonal changes in photosynthetic activity were primarily controlled by shifts in temperature. Ecosystem respiration was strongly correlated with changes in ecosystem photosynthesis during the growing season, suggesting important links between plant activity and mycorrhizae and microbial activity in the shallow layers of the peat. Only very low rates of respiration were observed during the winter months. During 2004, the peatland recorded a net annual gain of 144 g C m−2 year−1, the result of a difference between gross photosynthesis of 713 and total ecosystem respiration of 569 g C m−2 year−1.  相似文献   

8.
Little work has been done to quantify annual soil CO2 effluxes in the High Arctic region because of the difficulty in taking winter measurements. Since the effects of climate change are expected to be higher in Arctic than in temperate ecosystems, it is important that summer measurements are extended to cover the entire year. This study evaluates the quantity and quality of soil organic C (SOC) and seasonal controls of soil CO2 effluxes in three soils under three dominating types of vegetation (Dryas, Cassiope, and Salix) at Svalbard. Measurements included soil CO2 effluxes in the field and the laboratory, temperature, water content, and snow thickness. About 90% of the variation in soil respiration throughout 1 year was due to near-surface soil temperatures which ranged from −12 to +12 °C. Total annual soil CO2 effluxes varied from 103 g C m−2 at soils under Cassiope, 152 g C m−2 under Dryas sites, and 176 g C m−2 under Salix, with 20%, 14%, and 30%, respectively, being released during a 6-month winter period. The sensitivity of soil respiration with respect to soil temperature was the same year round and differences in winter CO2 effluxes at the three vegetation types were mainly related to subsurface soil temperatures controlled by snow depth. The quantity and quality of soil organic matter varied under the different vegetation types. Soils under Salix had the largest and most labile pool of SOC and were characterized by a long period of snow cover. In contrast, soils under Cassiope were more nutrient-poor, more acidic and held the smallest amount of total and labile SOC, whereas soils under Dryas remained snow-free most of the winter and therefore had the coldest winter conditions. Thus, winter soil respiration rates under Dryas and Cassiope were significantly lower than those under Salix; under Dryas this was mainly due to snow depth, under Cassiope this was a combination of snow depth and poor litter quality. It is concluded that winter respiration is highly variable across Arctic landscapes and depends on the spatial distribution of snow, which acts as a direct control on soil temperatures and indirect on vegetation types and thereby, the amount and quality of soil organic matter, which serve as additional important drivers of soil respiration.  相似文献   

9.
10.
The activity of heterotrophic soil microorganisms is usually limited by the availability and quality of carbon (C). Adding organic substances will thus trigger a microbial response. We studied the response in bacterial growth and respiration after the addition of low amounts of glucose. First we determined if additions of glucose, at concentrations which did not result in an exponential increase in respiration after the lag phase, still stimulated bacterial growth. The second aim was to determine the threshold concentration of glucose needed to induce bacterial growth. Adding glucose-C at 1000 μg g−1 soil resulted in an increased respiration rate, which was stable during 12 h, and then decreased without showing any exponential increase in respiration. Bacterial growth, determined as leucine incorporation, did not change compared to an unamended control during the first 12 h, but then increased to levels 5 times higher than in the control. Thus, after the lag phase, a period with increasing bacterial growth, but at the same time decreasing respiration rates, was found. Similar results, but with a more modest increase in bacterial growth, were found using 500 μg glucose-C g−1 soil. Adding 50–700 μg glucose-C g−1 resulted in increased respiration during 24 h correlating with the addition rate. In contrast, bacterial growth after 24 h was only stimulated by glucose additions >200 μg C g−1 soil. Thus, there was a threshold concentration of added substrate for inducing bacterial growth. Below the threshold concentration growth and respiration appear to be uncoupled.  相似文献   

11.
The objectives of this study were to investigate the effect of higher CO2 concentrations (500 and 700 μmol mol^-1) in atmosphere on total soil respiration and the contribution of root respiration to total soil respiration during seedling growth of Pinus sylvestris vat. sylvestriformis. During the four growing seasons (May-October) from 1999 to 2003, the seedlings were exposed to elevated concentrations of CO2 in open-top chambers. The total soil respiration and contribution of root respiration were measured using an LI-6400-09 soil CO2 flux chamber on June 15 and October 8, 2003. To separate root respiration from total soil respiration, three PVC cylinders were inserted approximately 30 cm deep into the soil in each chamber. There were marked diurnal changes in air and soil temperatures on June 15. Both the total soil respiration and the soil respiration without roots showed a strong diurnal pattern, increasing from before sunrise to about 14:00 in the afternoon and then decreasing before the next sunrise. No increase in the mean total soil respiration and mean soil respiration with roots severed was observed under the elevated CO2 treatments on June 15, 2003, as compared to the open field and control chamber with ambient CO2. However, on October 8, 2003, the total soil respiration and soil respiration with roots severed in the open field were lower than those in the control and elevated CO2 chambers. The mean contribution of root respiration measured on June 15, 2003, ranged from 8.3% to 30.5% and on October 8, 2003, from 20.6% to 48.6%.  相似文献   

12.
Plot trenching and root decomposition experiments were conducted in a warm-temperate oak chronosequence (40-year-old, 48-year-old, 80-year-old, and 143-year-old) in China. We partitioned total soil surface CO2 efflux (RS) into heterotrophic (RH) and rhizospheric (RR) components across the growing season of 2009. We found that the temporal variation of RR and RH can be well explained by soil temperature (T5) at 5 cm depth using exponential equations for all forests. However, RR of 40-year-old and 48-year-old forests peaked in September, while their T5 peaks occurred in August. RR of 80-year-old and 143-year-old forests showed a similar pattern to T5. The contribution of RR to RS (RC) of 40-year-old and 48-year-old forests presented a second peak in September. Seasonal variation of RR may be accounted for by the different successional stages. Cumulative RH and RR during the growing season varied with forest age. The estimated RH values for 40-year-old, 48-year-old, 80-year-old and 143-year-old forests averaged 431.72, 452.02, 484.62 and 678.93 g C m−2, respectively, while the corresponding values of RR averaged 191.94, 206.51, 321.13 and 153.03 g C m−2. The estimated RC increased from 30.78% in the 40-year-old forest to 39.85% in the 80-year-old forest and then declined to 18.39% in the 143-year-old forest. We found soil organic carbon (SOC), especially the light fraction organic carbon (LFOC), stock at 0-10 cm soil depth correlated well with RH. There was no significant relationship between RR and fine root biomass regardless of stand age. Measured apparent temperature sensitivity (Q10) of RH (3.93 ± 0.27) was significantly higher than that of RR (2.78 ± 0.73). Capillary porosity decreased as stand age increased and it was negatively correlated to cumulative RS. Our results emphasize the importance of partitioning soil respiration in evaluating the stand age effect on soil respiration and its significance to future model construction.  相似文献   

13.
The need to identify microbial community parameters that predict microbial activity is becoming more urgent, due to the desire to manage microbial communities for ecosystem services as well as the desire to incorporate microbial community parameters within ecosystem models. In dryland agroecosystems, microbial biomass C (MBC) can be increased by adopting alternative management strategies that increase crop residue retention, nutrient reserves, improve soil structure and result in greater water retention. Changes in MBC could subsequently affect microbial activities related to decomposition, C stabilization and sequestration. We hypothesized that MBC and potential microbial activities that broadly relate to decomposition (basal and substrate-induced respiration, N mineralization, and β-glucosidase and arylsulfatase enzyme activities) would be similarly affected by no-till, dryland winter wheat rotations distributed along a potential evapotranspiration (PET) gradient in eastern Colorado. Microbial biomass was smaller in March 2004 than in November 2003 (417 vs. 231 μg g−1 soil), and consistently smaller in soils from the high PET soil (191 μg g−1) than in the medium and low PET soils (379 and 398 μg g−1, respectively). Among treatments, MBC was largest under perennial grass (398 μg g−1). Potential microbial activities did not consistently follow the same trends as MBC, and the only activities significantly correlated with MBC were β-glucosidase (r = 0.61) and substrate-induced respiration (r = 0.27). In contrast to MBC, specific microbial activities (expressed on a per MBC basis) were greatest in the high PET soils. Specific but not total activities were correlated with microbial community structure, which was determined in a previous study. High specific activity in low biomass, high PET soils may be due to higher microbial maintenance requirements, as well as to the unique microbial community structure (lower bacterial-to-fungal fatty acid ratio and lower 17:0 cy-to-16:1ω7c stress ratio) associated with these soils. In conclusion, microbial biomass should not be utilized as the sole predictor of microbial activity when comparing soils with different community structures and levels of physiological stress, due to the influence of these factors on specific activity.  相似文献   

14.
Long term flux measurements of different crop species are necessary to improve our understanding of management and climate effects on carbon flux variability as well as cropland potential in terrestrial carbon sequestration. The main objectives of this study were to analyse the seasonal dynamics of CO2 fluxes and to establish the effects of climate and cropland management on the annual carbon balance.CO2 fluxes were measured by means of the eddy correlation (EC) method over two cropland sites, Auradé and Lamasquère, in South West France for a succession of three crops: rapeseed, winter wheat and sunflower at Auradé, and triticale, maize and winter wheat at Lamasquère. The net ecosystem exchange (NEE) was partitioned into gross ecosystem production (GEP) and ecosystem respiration (RE) and was integrated over the year to compute net ecosystem production (NEP). Different methodologies tested for NEP computation are discussed and a methodology for estimating NEP uncertainty is presented.NEP values ranged between −369 ± 33 g C m−2 y−1 for winter wheat at Lamasquère in 2007 and 28 ± 18 g C m−2 y−1 for sunflower at Auradé in 2007. These values were in good agreement with NEP values reported in the literature, except for maize which exhibited a low development compared to the literature. NEP was strongly influenced by the length of the net carbon assimilation period and by interannual climate variability. The warm 2007 winter stimulated early growth of winter wheat, causing large differences in GEP, RE and NEE dynamics for winter wheat when compared to 2006. Management had a strong impact on CO2 flux dynamics and on NEP. Ploughing interrupted net assimilation during voluntary re-growth periods, but it had a negligible short term effect when it occurred on bare soil. Re-growth events after harvest appeared to limit carbon loss: at Lamasquère in 2005 re-growth contributed to store up to 50 g C m−2. Differences in NEE response to climatic variables (VPD, light quality) and vegetation index were addressed and discussed.Net biome production (NBP) was calculated yearly based on NEP and considering carbon input through organic fertilizer and carbon output through harvest. For the three crops, the mean NBP at Auradé indicated a nearly carbon balanced ecosystem, whereas Lamasquère lost about 100 g C m−2 y−1; therefore, the ecosystem behaved as a carbon source despite the fact that carbon was imported through organic fertilizer. Carbon exportation through harvest was the main cause of this difference between the two sites, and it was explained by the farm production type. Lamasquère is a cattle breeding farm, exporting most of the aboveground biomass for cattle bedding and feeding, whereas Auradé is a cereal production farm, exporting only seeds.  相似文献   

15.
The addition of small or trace amounts of carbon to soils can result in the release of 2-5 times more C as CO2 than was added in the original solution. The identity of the microorganisms responsible for these so-called trigger effects remains largely unknown. This paper reports on the response of individual bacterial taxa to the addition of a range of 14C-glucose concentrations (150, 50 and 15 and 0 μg C g−1 soil) similar to the low levels of labile C found in soil. Taxon-specific responses were identified using a modification of the stable isotope probing (SIP) protocol and the recovery of [14C] labelled ribosomal RNA using equilibrium density gradient centrifugation. This provided good resolution of the ‘heavy’ fractions ([14C] labelled RNA) from the ‘light’ fractions ([12C] unlabelled RNA). The extent of the separation was verified using autoradiography. The addition of [14C] glucose at all concentrations was characterised by changes in the relative intensity of particular bands. Canonical correspondence analysis (CCA) showed that the rRNA response in both the ‘heavy’ and ‘light’ fractions differed according to the concentration of glucose added but was most pronounced in soils amended with 150 μg C g−1 soil. In the ‘heavy RNA’ fractions there was a clear separation between soils amended with 150 μg C g−1 soil and those receiving 50 and 15 μg C g−1 soil indicating that at low C inputs the microbial community response is quite distinct from that seen at higher concentrations. To investigate these differences further, bands that changed in relative intensity following amendment were excised from the DGGE gels, reamplified and sequenced. Sequence analysis identified 8 taxa that responded to glucose amendment (Bacillus, Pseudomonas, Burkholderia, Bradyrhizobium, Actinobacteria, Nitrosomonas, Acidobacteria and an uncultured β-proteobacteria). These results show that radioisotope probing (RNA-RIP) can be used successfully to study the fate of labile C substrates, such as glucose, in soil.  相似文献   

16.
Organic carbon (OC) is generally low in Alabama (U.S.A.) soils and varies considerably with cropping systems. Information on decomposition rates of the added C is a prerequisite to designing strategies that improve C sequestration in farming systems. Different models including exponential models have been used to describe OC mineralization in soils as well as to describe its potential as CO2 to be released into the environment. We investigated the decomposition of broiler litter added to ten non-calcareous soils (Appling, Troup, Cecil, Decatur, Sucarnoochee, Linker, Hartsells, Dothan, Maytag, and Colbert soils). A non-linear regression approach for N mineralization was used to estimate the potentially mineralizable OC pools (Co) and the first-order rate constant (k) in the soil samples. Results showed that the non-amended soils have distinct differences in their ability to release their native OC as CO2 and can be divided into four groups depending on their potentially mineralizable C (Co) and their ability to protect stable organic matter. Sucarnoochee soil represents the first group and contains a moderate amount of OC (11.4 g C kg−1) but had the highest Co (7.30 g C kg−1 soil). The second distinct group of soils has Co varying between 5.50 and 5.00 g C kg−1 soil (Decatur, Hartsells, Dothan, and Maytag). The third group has Co between 5.00 and 4.00 (Appling, Cecil, and Linker). The fourth group has Co less than 4.00 g C kg−1 soil (Troup and Colbert). Half-life of C remaining in non-amended soils varied from 26 days in Maytag soil to 139 days in Cecil soil. The OC in these non-amended soils represents a very stable form of organic C and thus, not easily decomposed by soil microorganisms. In the broiler litter-amended soils, the Co varied from 3.82 g C kg−1 in Appling soil amended with broiler litter 1-7.04 g C kg−1 soil in Maytag amended with broiler litter 2. Decomposition of the added OC proceeded in two phases with less than 31% decomposed in 43 days. Potentially mineralizable organic C (Co) was related to soil organic C (r = 0.661**) and soil C/N ratio (r = 0.819*).  相似文献   

17.
2011年7月至2012年3月,利用LI-8100土壤CO2通量系统测定了淮南市大通煤矸石充填复垦区草地、灌丛、小乔木林、大乔木林土壤呼吸强度及其相关影响因子.结果显示,煤矸石充填复垦区4种植被类型下土壤呼吸强度的昼夜及季节变化均呈单峰曲线形式,最大值出现在夏季的12:00-16:00间,最小值出现在冬季的4:00左右;不同植被类型下土壤呼吸强度差异显著(p<0.05),且土壤呼吸强度有强到弱的顺序呈现:草地>灌丛>小乔木林>大乔木林.4种植被土壤CO2-C年释放通量分别为(999.74±62.26) g/(m2· a),(908.49±72.41) g/(m2· a),(869.22±56.23) g/(m2· a),(726.10±63.01) g/(m2· a),故考虑植被的碳减排效应,在煤矸石充填复垦区可以多种植乔木、灌木,而尽量少植人工草坪;复垦区土壤呼吸除受植被类型影响外,主要受10 cm土层土壤温度的影响,各植被类型土壤呼吸强度对土壤温度的指数模型均可以解释88%以上的土壤呼吸变异;草地、灌丛、小乔木林、大乔木林碳排放对温度的敏感性Q10值分别为:2.57,2.71,2.96和3.67.  相似文献   

18.
A long-term field experiment was conducted to examine the influence of mineral fertilizer and organic manure on the equilibrium dynamics of soil organic C in an intensively cultivated fluvo-aquic soil in the Fengqiu State Key Agro-Ecological Experimental Station (Fengqiu county, Henan province, China) since September 1989. Soil CO2 flux was measured during the maize and wheat growing seasons in 2002-2003 and 2004 to evaluate the response of soil respiration to additions and/or alterations in mineral fertilizer, organic manure and various environmental factors. The study included seven treatments: organic manure (OM), half-organic manure plus half-fertilizer N (NOM), fertilizer NPK (NPK), fertilizer NP (NP), fertilizer NK (NK), fertilizer PK (PK) and control (CK). Organic C in soil and the soil heavy fraction (organo-mineral complex) was increased from 4.47 to 8.61 mg C g−1 and from 3.32 to 5.68 mg C g−1, respectively, after the 13 yr application of organic manure. In contrast, organic C and the soil heavy fraction increased in NPK soil to only 5.41 and 4.38 mg C g−1, respectively. In the CK treatment, these parameters actually decreased from the initial C concentrations (4.47 and 3.32 mg C g−1) to 3.77 and 3.11 mg C g−1, respectively. Therefore, organic manure efficiently elevated soil organic C. However, only 66% of the increased soil organic C was combined with clay minerals in the OM treatment. Cumulative soil CO2 emissions from inter-row soil in the OM and NPK treatments were 228 and 188 g C m−2 during the 2002 maize growing season, 132 and 123 g C m−2 during the 2002/2003 wheat growing season, and 401 and 346 g C m−2 yr−1 in 2002-2003, respectively. However, during the 2004 maize growing season, cumulative soil CO2 emissions were as high as 617 and 556 g C m−2, respectively, due to the contribution of rhizosphere respiration. The addition of organic manure contributed to a 16% increase in soil CO2 emission in 2002-2003 (compared to NPK), where only 27%, 36% and 24% of applied organic C was released as CO2 during the 2002 and 2004 maize growing seasons and in 2002-2003, respectively. During the 2002/2003 wheat growing season, soil CO2 flux was significantly affected by soil temperature below 20 °C, but by soil moisture (WFPS) during the 2004 maize growing season at soil temperatures above 18 °C. Optimum soil WFPS for soil CO2 flux was approximately 70%. When WFPS was below 50%, it no longer had a significant impact on soil CO2 flux during the 2002 maize growing season. This study indicates the application of organic manure composted with wheat straw may be a preferred strategy for increasing soil organic C and sequestering C in soil.  相似文献   

19.
Carbon dioxide, water vapour and energy fluxes were measured above and within a maritime pine forest during an atypical year with long-lasting reduced soil water availability. Energy balance closure was adequately good at both levels. As compared with what is usually observed at this site the ecosystem dissipated less energy via latent heat flux and more via sensible heat flux. The understorey canopy was responsible for a variable, significant component of the whole canopy fluxes of water vapour and carbon dioxide. The annual contribution of the understorey was 38% (154 mm) of the overall evaporation (399 mm) and 32% (89 mm) of the overall sensible heat flux (274 mm). The participation of the understorey reached 45% of the overall evaporation and 30% of the daytime overall assimilation during significant soil water deficit periods in summertime. Even during winter, understorey photosynthesis was consistent as it compensated soil and understorey respiration. The ecosystem behaved as a sink of carbon, with a negative annual carbon budget (−57 g C m−2). However, due to high soil water deficit, the annual ecosystem GPP was 40% less than usually observed at this site. This budget resulted from a sink of −131 g C m−2 for the overstorey and a source of +74 g C m−2 for the understorey. Moreover, on an annual basis the overstorey layer contributed to almost two-thirds of the ecosystem respiration. Finally, the effect of long-lasting soil water deficit on the maritime pine forest was found more important than the effect of the heat wave and drought of summer 2003.  相似文献   

20.
The diurnal and seasonal variations of soil respiration (SR) were studied at a subtropical mangrove wetland in the Jiulong River Estuary from May 2010 to April 2011.SR rates were measured continuously from 08:00 to 06:00 local time (24-h time system) on July8–9 and October 3–4,2010;and January 15–16 and April 11–12,2011.Similar patterns in the diurnal variation of SR were observed on October 2–3 and April 11–12,with the maximum values at 14:00 and the minimum at 00:00.However,the diurnal dynamics of SR on July 8–9,2010 and January 15–16,2011 showed diferent patterns,with the maximum values at 08:00–10:00 on above sampling dates and the minimum at 22:00 on July 8 and at 04:00 on January 16.The daily mean values of SR approximated to the values measured at 08:00.SR fluctuated with distinct seasonal patterns.The seasonal variation was characterized by a mono-peak pattern,with the highest rate (6.18μmol CO2m-2s-1) in July and the lowest rate (0.36μmol CO2m-2s-1) in December.The results showed that the variation of SR in mangrove wetland was mainly controlled by soil temperature,and there was no significant correlation between SR and soil water content.It also implied that the model of SR in mangrove wetland should not only consider the efect of soil temperature,but also incorporate other factors,such as water level,precipitation,microbial activity and photosynthesis,which also could affect SR.  相似文献   

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