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1.
Global climate change can potentially increase the frequency of climate anomalies. Anomalously warm years may cause an increase in soil nitrogen (N) availability by stimulating N mineralization. To date, most studies addressing the effects of ecosystem warming have been conducted in relatively cold ecosystems and few studies have addressed impacts of interannual as opposed to continuous, multiyear warming. In this study, 12 intact soil monoliths were excavated from a tallgrass prairie site near Purcell, Oklahoma, USA and divided among four large flux chambers (EcoCELLs). During the first year, all four EcoCELLs were subjected to Oklahoma air temperatures and precipitation. During the second year, air temperature in two EcoCELLs was increased by 4 °C throughout the year resulting in an increase in soil temperature of 2.3 °C at 7.5 cm depth. During the third and fourth years, temperatures in the warmed EcoCELL returned back to 'normal' conditions. During the warming year, vegetation N content was not significantly affected by the warming treatment suggesting no change in N availability. Other N availability indicators (soil solution chemistry, leaching, and N adsorption by ion exchange resins) did not show any effect of warming. Soil solution, leaching, and ion exchange resins showed a large pulse of NH4+ at the start of the study most likely due to disturbance caused by monolith excavation and transport but these effects were short-lived and had disappeared before the treatment started. The lack of a clear warming effect may be explained by a reduction in soil moisture in the warming treatments compared with the controls offsetting a potential stimulation of N mineralization in response to increased temperatures. As a result, effects of an anomalously warm year on N availability in warmer ecosystems may be small compared with colder ecosystems but are likely to depend on soil moisture status.  相似文献   

2.
Partitioning soil CO2 efflux into autotrophic (RA) and heterotrophic (RH) components is crucial for understanding their differential responses to climate change. We conducted a long‐term experiment (2000–2005) to investigate effects of warming 2°C and yearly clipping on soil CO2 efflux and its components (i.e. RA and RH) in a tallgrass prairie ecosystem. Interannual variability of these fluxes was also examined. Deep collars (70 cm) were inserted into soil to measure RH. RA was quantified as the difference between soil CO2 efflux and RH. Warming treatment significantly stimulated soil CO2 efflux and its components (i.e. RA and RH) in most years. In contrast, yearly clipping significantly reduced soil CO2 efflux only in the last 2 years, although it decreased RH in every year of the study. Temperature sensitivity (i.e. apparent Q10 values) of soil CO2 efflux was slightly lower under warming (P>0.05) and reduced considerably by clipping (P<0.05) compared with that in the control. On average over the 4 years, RH accounted for approximately 65% of soil CO2 efflux with a range from 58% to 73% in the four treatments. Over seasons, the contribution of RH to soil CO2 efflux reached a maximum in winter (∼90%) and a minimum in summer (∼35%). Annual soil CO2 efflux did not vary substantially among years as precipitation did. The interannual variability of soil CO2 efflux may be mainly caused by precipitation distribution and summer severe drought. Our results suggest that the effects of warming and yearly clipping on soil CO2 efflux and its components did not result in significant changes in RH or RA contribution, and rainfall timing may be more important in determining interannual variability of soil CO2 efflux than the amount of annual precipitation.  相似文献   

3.
Thermal adaptations of soil microorganisms could mitigate or facilitate global warming effects on soil organic matter (SOM) decomposition and soil CO2 efflux. We incubated soil from warmed and control subplots of a forest soil warming experiment to assess whether 9 years of soil warming affected the rates and the temperature sensitivity of the soil CO2 efflux, extracellular enzyme activities, microbial efficiency, and gross N mineralization. Mineral soil (0–10 cm depth) was incubated at temperatures ranging from 3 to 23 °C. No adaptations to long‐term warming were observed regarding the heterotrophic soil CO2 efflux (R10 warmed: 2.31 ± 0.15 μmol m?2 s?1, control: 2.34 ± 0.29 μmol m?2 s?1; Q10 warmed: 2.45 ± 0.06, control: 2.45 ± 0.04). Potential enzyme activities increased with incubation temperature, but the temperature sensitivity of the enzymes did not differ between the warmed and the control soils. The ratio of C : N acquiring enzyme activities was significantly higher in the warmed soil. Microbial biomass‐specific respiration rates increased with incubation temperature, but the rates and the temperature sensitivity (Q10 warmed: 2.54 ± 0.23, control 2.75 ± 0.17) did not differ between warmed and control soils. Microbial substrate use efficiency (SUE) declined with increasing incubation temperature in both, warmed and control, soils. SUE and its temperature sensitivity (Q10 warmed: 0.84 ± 0.03, control: 0.88 ± 0.01) did not differ between warmed and control soils either. Gross N mineralization was invariant to incubation temperature and was not affected by long‐term soil warming. Our results indicate that thermal adaptations of the microbial decomposer community are unlikely to occur in C‐rich calcareous temperate forest soils.  相似文献   

4.
Microbial decomposition of soil organic matter produces a major flux of CO2 from terrestrial ecosystems and can act as a feedback to climate change. Although climate‐carbon models suggest that warming will accelerate the release of CO2 from soils, the magnitude of this feedback is uncertain, mostly due to uncertainty in the temperature sensitivity of soil organic matter decomposition. We examined how warming and altered precipitation affected the rate and temperature sensitivity of heterotrophic respiration (Rh) at the Boston‐Area Climate Experiment, in Massachusetts, USA. We measured Rh inside deep collars that excluded plant roots and litter inputs. In this mesic ecosystem, Rh responded strongly to precipitation. Drought reduced Rh, both annually and during the growing season. Warming increased Rh only in early spring. During the summer, when Rh was highest, we found evidence of threshold, hysteretic responses to soil moisture: Rh decreased sharply when volumetric soil moisture dropped below ~15% or exceeded ~26%, but Rh increased more gradually when soil moisture rose from the lower threshold. The effect of climate treatments on the temperature sensitivity of Rh depended on the season. Apparent Q10 decreased with high warming (~3.5 °C) in spring and fall. Presumably due to limiting soil moisture, warming and precipitation treatments did not affect apparent Q10 in summer. Drought decreased apparent Q10 in fall compared to ambient and wet precipitation treatments. To our knowledge, this is the first field study to examine the response of Rh and its temperature sensitivity to the combined effects of warming and altered precipitation. Our results highlight the complex responses of Rh to soil moisture, and to our knowledge identify for the first time the seasonal variation in the temperature sensitivity of microbial respiration in the field. We emphasize the importance of adequately simulating responses such as these when modeling trajectories of soil carbon stocks under climate change scenarios.  相似文献   

5.
The response of heterotrophic CO2 flux to soil warming   总被引:3,自引:0,他引:3  
In a forest ecosystem at steady state, net carbon (C) assimilation by plants and C loss through soil and litter decomposition by heterotrophic organisms are balanced. However, a perturbation to the system, such as increased mean soil temperature, will lead to faster decay, enhancing CO2 release from decomposers, and thus upsetting the balance. Recent in situ experiments have indicated that the stimulation of soil respiration following a step increase in annual average soil temperature declines over time. One possible explanation for this decline may be changes in substrate availability. This hypothesis is examined by using the ecosystem model G'DAY, which simulates C and nitrogen (N) dynamics in plants and soil. We applied the model to observations from a soil‐warming experiment in a Norway spruce (Picea abies (L.) Karst.) stand by simulating a step increase of soil temperature. The model provided a good qualitative reproduction of the observed reduction of heterotrophic respiration (Rh) under sustained warming. The simulations showed how the combined effects of faster turnover and reduced substrate availability lead to a transient increase of Rh. The simulated annual increase in Rh from soil was 60% in the first year after perturbation but decreased to 30% after a decade. One conclusion from the analysis of the simulations is that Rh can decrease even though the temperature response function for decomposition remains unchanged. G'DAY suggests that acclimation of Rh to soil warming is partly an effect of substrate depletion of labile C pools during the first decade of warming as a result of accelerated rates of mineralization. The response is attributed mainly to changing levels of C in pools with short time constants, reflecting the importance of high‐quality soil C fractions. Changes of the structure or physiology of the decomposer community were not invoked. Therefore, it becomes a question of definition whether the simulated dynamics of the declining response of CO2 release to the warming should be named acclimation or seen as a natural part of the system dynamics.  相似文献   

6.
Global warming has the potential to increase soil respiration (RS), one of the major fluxes in the global carbon (C) cycle. RS consists of an autotrophic (RA) and a heterotrophic (RH) component. We combined a soil warming experiment with a trenching experiment to assess how RS, RA, and RH are affected. The experiment was conducted in a mature forest dominated by Norway spruce. The site is located in the Austrian Alps on dolomitic bedrock. We warmed the soil of undisturbed and trenched plots by means of heating cables 4 °C above ambient during the snow‐free seasons of 2005 and 2006. Soil warming increased the CO2 efflux from control plots (RS) by ∼45% during 2005 and ∼47% during 2006. The CO2 efflux from trenched plots (RH) increased by ∼39% during 2005 and ∼45% during 2006. Similar responses of RS and RH indicated that the autotrophic and heterotrophic components of RS responded equally to the temperature increase. Thirty‐five to forty percent or 1 t C ha−1 yr−1 of the overall annual increase in RS (2.8 t C ha−1 yr−1) was autotrophic. The remaining, heterotrophic part of soil respiration (1.8 t C ha−1 yr−1), represented the warming‐induced C loss from the soil. The autotrophic component showed a distinct seasonal pattern. Contribution of RA to RS was highest during summer. Seasonally derived Q10 values reflected this pattern and were correspondingly high (5.3–9.3). The autotrophic CO2 efflux increase due to the 4 °C warming implied a Q10 of 2.9. Hence, seasonally derived Q10 of RA did not solely reflect the seasonal soil temperature development.  相似文献   

7.
Climate change may considerably impact the carbon (C) dynamics and C stocks of forest soils. To assess the combined effects of warming and reduced precipitation on soil CO2 efflux, we conducted a two‐way factorial manipulation experiment (4 °C soil warming + throughfall exclusion) in a temperate spruce forest from 2008 until 2010. Soil was warmed by heating cables throughout the growing seasons. Soil drought was simulated by throughfall exclusions with three 100 m2 roofs during 25 days in July/August 2008 and 2009. Soil warming permanently increased the CO2 efflux from soil, whereas throughfall exclusion led to a sharp decrease in soil CO2 efflux (45% and 50% reduction during roof installation in 2008 and 2009, respectively). In 2008, CO2 efflux did not recover after natural rewetting and remained lowered until autumn. In 2009, CO2 efflux recovered shortly after rewetting, but relapsed again for several weeks. Drought offset the increase in soil CO2 efflux by warming in 2008 (growing season CO2 efflux in t C ha?1: control: 7.1 ± 1.0; warmed: 9.5 ± 1.7; warmed + roof: 7.4 ± 0.3; roof: 5.9 ± 0.4) and in 2009 (control: 7.6 ± 0.8; warmed + roof: 8.3 ± 1.0). Throughfall exclusion mainly affected the organic layer and the top 5 cm of the mineral soil. Radiocarbon data suggest that heterotrophic and autotrophic respiration were affected to the same extent by soil warming and drying. Microbial biomass in the mineral soil (0–5 cm) was not affected by the treatments. Our results suggest that warming causes significant C losses from the soil as long as precipitation patterns remain steady at our site. If summer droughts become more severe in the future, warming induced C losses will likely be offset by reduced soil CO2 efflux during and after summer drought.  相似文献   

8.
A non‐vented non‐steady state flow‐through chamber and a non‐vented non‐steady state non‐flow‐through chamber technique were used to measure CO2 efflux of a young Scots pine forest on a fertile till soil in southern Finland. Soil temperature, soil moisture and soil CO2 concentration were measured concurrently with CO2 efflux for two and a half successive years. The CO2 efflux showed a seasonal pattern, effluxes ranging from low 0.0–0.1 g CO2 m ? 2 h ? 1 in winter to peak values of 2.3 g CO2 m ? 2 h ? 1 occurring in late June and in July. The daily average effluxes in July measured by flow through chambers were 1.23 and 0.98 g CO2 m ? 2 h ? 1 in 1998 and 1999, respectively. The annual accumulated CO2 efflux was 3117 and 3326 g CO2 m ? 2 in 1998 and 1999, respectively. The spatial variation in CO2 efflux was high (CV 0.18–0.45) and increased with increasing efflux. Soil air CO2 concentration showed similar seasonal pattern the peak concentrations occurring in July–August. The CO2 concentrations ranged from 580 to 780 µ mol mol ? 1 in the humus layer to 13 620–14 470 µ mol mol ? 1 in the C‐horizon. In winter the soil air CO2 concentrations were lower, especially in deeper soil layers. Drought decreased CO2 efflux and soil air CO2 concentration. The in situ comparison on forest soil between the chamber methods showed the non‐flow‐through chamber to give ~~50% lower efflux values than that of the flow‐through chamber. When calibrated against known CO2 efflux ranging from 0.4 to 0.8 g CO2 m ? 2 h ? 1 generated with a diffusion box method developed by Widén and Lindroth [Acta Universitatis Agriculturae Suecia Silvestria, 2001], the flow‐through chamber gave equal effluxes at the lower end of the calibration range, but overestimated high effluxes by 20%. Non‐flow‐through chamber underestimated the CO2 efflux by 30%.  相似文献   

9.
Liu  Xiaozhong  Wan  Shiqiang  Su  Bo  Hui  Dafeng  Luo  Yiqi 《Plant and Soil》2002,240(2):213-223
Although CO2 efflux plays a critical role in carbon exchange between the biosphere and atmosphere, our understanding of its regulation by soil moisture is rather limited. This study was designed to examine the relationship between soil CO2 efflux and soil moisture in a natural ecosystem by taking advantage of the historically long drought period from 29 July to 21 September 2000 in the southern Central Great Plain, USA. At the end of August when soil moisture content at the top 50 mm was reduced to less than 50 g kg–1 gravimetrically, we applied 8 levels of water treatments (simulated to rainfall of 0, 10, 25, 50, 100, 150, 200, and 300 mm) with three replicates to 24 plots in a Tallgrass Prairie ecosystem in Central Oklahoma, USA. In order to quantify root-free soil CO2 efflux, we applied the same 8 levels of water treatments to 24 500-mm soil columns using soil from field adjacent to the experimental plots. We characterized dynamic patterns of soil moisture and soil CO2 efflux over the experimental period of 21 days. Both soil moisture content and CO2 efflux showed dramatic increases immediately after the water addition, followed by a gradual decline. The time courses in response to water treatments are well described by Y=Y0+ate–bt, where Y is either soil moisture or CO2 efflux, t is time, Y 0, a, and b are coefficients. Among the 8 water treatments, the maximal soil CO2 efflux rate occurred at the 50 mm water level in the field and 100 mm in the root-free soil 1 day after the treatment. The maximal soil CO2 efflux gradually shifted to higher water levels as the experiment continued. We found the relationship between soil CO2 efflux and soil moisture using the data from the 21-day experiment was highly scattered, suggesting complex mechanisms determining soil CO2 efflux by soil moisture.  相似文献   

10.
With the large extent and great amount of soil carbon (C) storage, drylands play an important role in terrestrial C balance and feedbacks to climate change. Yet, how dryland soils respond to gradual and concomitant changes in multiple global change drivers [e.g., temperature (Ts), precipitation (Ppt), and atmospheric [CO2] (CO2)] has rarely been studied. We used a process‐based ecosystem model patch arid land simulator to simulate dryland soil respiration (Rs) and C pool size (Cs) changes to abrupt vs. gradual and single vs. combined alterations in Ts, Ppt and CO2 at multiple treatment levels. Results showed that abrupt perturbations generally resulted in larger Rs and had longer differentiated impacts than did gradual perturbations. Rs was stimulated by increases in Ts, Ppt, and CO2 in a nonlinear fashion (e.g., parabolically or asymptotically) but suppressed by Ppt reduction. Warming mainly stimulated heterotrophic Rs (i.e., Rh) whereas Ppt and CO2 influenced autotrophic Rs (i.e., Ra). The combined effects of warming, Ppt, and CO2 were nonadditive of primary single‐factor effects as a result of substantial interactions among these factors. Warming amplified the effects of both Ppt addition and CO2 elevation whereas Ppt addition and CO2 elevation counteracted with each other. Precipitation reduction either magnified or suppressed warming and CO2 effects, depending on the magnitude of factor's alteration and the components of Rs (Ra or Rh) being examined. Overall, Ppt had dominant influence on dryland Rs and Cs over Ts and CO2. Increasing Ppt individually or in combination with Ts and CO2 benefited soil C sequestration. We therefore suggested that global change experimental studies for dryland ecosystems should focus more on the effects of precipitation regime changes and the combined effects of Ppt with other global change factors (e.g., Ts, CO2, and N deposition).  相似文献   

11.
A positive soil carbon (C)‐climate feedback is embedded into the climatic models of the IPCC. However, recent global syntheses indicate that the temperature sensitivity of soil respiration (RS) in drylands, the largest biome on Earth, is actually lower in warmed than in control plots. Consequently, soil C losses with future warming are expected to be low compared with other biomes. Nevertheless, the empirical basis for these global extrapolations is still poor in drylands, due to the low number of field experiments testing the pathways behind the long‐term responses of soil respiration (RS) to warming. Importantly, global drylands are covered with biocrusts (communities formed by bryophytes, lichens, cyanobacteria, fungi, and bacteria), and thus, RS responses to warming may be driven by both autotrophic and heterotrophic pathways. Here, we evaluated the effects of 8‐year experimental warming on RS, and the different pathways involved, in a biocrust‐dominated dryland in southern Spain. We also assessed the overall impacts on soil organic C (SOC) accumulation over time. Across the years and biocrust cover levels, warming reduced RS by 0.30 μmol CO2 m?2 s?1 (95% CI = ?0.24 to 0.84), although the negative warming effects were only significant after 3 years of elevated temperatures in areas with low initial biocrust cover. We found support for different pathways regulating the warming‐induced reduction in RS at areas with low (microbial thermal acclimation via reduced soil mass‐specific respiration and β‐glucosidase enzymatic activity) vs. high (microbial thermal acclimation jointly with a reduction in autotrophic respiration from decreased lichen cover) initial biocrust cover. Our 8‐year experimental study shows a reduction in soil respiration with warming and highlights that biocrusts should be explicitly included in modeling efforts aimed to quantify the soil C–climate feedback in drylands.  相似文献   

12.
熊沛  徐振锋  林波  刘庆 《植物生态学报》2010,34(12):1369-1376
冬季的土壤呼吸是生态系统呼吸的重要组成部分, 对气候变化的响应可能更为敏感。该文采用红外辐射加热器模拟土壤增温, 研究了岷江上游华山松(Pinus armandii)人工林冬季的土壤呼吸、微生物生物量及无机氮库对模拟增温的响应。结果表明: 在冬季(2009年11月-翌年3月), 模拟增温往往能显著提高土壤呼吸速率, 平均增幅达31.4%; 同样模拟增温使土壤微生物生物量碳、氮分别增加23.2%和22.7%, 而对微生物生物量碳氮比没有影响, 温度升高显著促进了微生物的生长, 但没有改变微生物的群落结构; 增温样地土壤的NO3 --N和NH4 +-N浓度较对照分别增加了38.5%和12.3%, 增温显著提高了土壤的可溶性无机氮含量。综上所述, 该区针叶林冬季土壤呼吸、微生物生长和养分矿化对未来气候变暖非常敏感。  相似文献   

13.
A simple estimation of heterotrophic respiration can be obtained analytically as the y-intercept of the linear regression between soil-surface CO2 efflux and root biomass. In the present study, a development of this indirect methodology is presented by taking into consideration both the temporal variation and the spatial heterogeneity of heterotrophic respiration. For this purpose, soil CO2 efflux, soil carbon content and main stand characteristics were estimated in seven evergreen forest ecosystems along an elevation gradient ranging from 250 to 1740 m. For each site and for each sampling date the measured soil CO2 efflux (R S) was predicted with the model R S = a × S C + b × R D ± ε, where S C is soil carbon content per unit area to a depth of 30 cm and R D is the root density of the 2–5 mm root class. Regressions with statistically significant a and b coefficients allowed the indirect separation of the two components of soil CO2 efflux. Considering that the different sampling dates were characterized by different soil temperature, it was possible to investigate the temporal and thermal dependency of autotrophic and heterotrophic respiration. It was estimated that annual autotrophic respiration accounts for 16–58% of total soil CO2 efflux in the seven different evergreen ecosystems. In addition, our observations show a decrease of annual autotrophic respiration at increasing availability of soil nitrogen. Section Editor: A. Hodge  相似文献   

14.
This study investigated the spatial and temporal variation in soil carbon dioxide (CO2) efflux and its relationship with soil temperature, soil moisture and rainfall in a forest near Manaus, Amazonas, Brazil. The mean rate of efflux was 6.45±0.25 SE μmol CO2 m?2s?1 at 25.6±0.22 SE°C (5 cm depth) ranging from 4.35 to 9.76 μmol CO2 m?2s?1; diel changes in efflux were correlated with soil temperature (r2=0.60). However, the efflux response to the diel cycle in temperature was not always a clear exponential function. During period of low soil water content, temperature in deeper layers had a better relationship with CO2 efflux than with the temperature nearer the soil surface. Soil water content may limit CO2 production during the drying‐down period that appeared to be an important factor controlling the efflux rate (r2=0.39). On the other hand, during the rewetting period microbial activity may be the main controlling factor, which may quickly induce very high rates of efflux. The CO2 flux chamber was adapted to mimic the effects of rainfall on soil CO2 efflux and the results showed that efflux rates reduced 30% immediately after a rainfall event. Measurements of the CO2 concentration gradient in the soil profile showed a buildup in the concentration of CO2 after rain on the top soil. This higher CO2 concentration developed shortly after rainfall when the soil pores in the upper layers were filled with water, which created a barrier for gas exchange between the soil and the atmosphere.  相似文献   

15.
Soil surface carbon dioxide (CO2) flux (RS) was measured for 2 years at the Boreal Soil and Air Warming Experiment site near Thompson, MB, Canada. The experimental design was a complete random block design that consisted of four replicate blocks, with each block containing a 15 m × 15 m control and heated plot. Black spruce [Picea mariana (Mill.) BSP] was the overstory species and Epilobium angustifolium was the dominant understory. Soil temperature was maintained (~5 °C) above the control soil temperature using electric cables inside water filled polyethylene tubing for each heated plot. Air inside a 7.3‐m‐diameter chamber, centered in the soil warming plot, contained approximately nine black spruce trees was heated ~5 °C above control ambient air temperature allowing for the testing of soil‐only warming and soil+air warming. Soil surface CO2 flux (RS) was positively correlated (P < 0.0001) to soil temperature at 10 cm depth. Soil surface CO2 flux (RS) was 24% greater in the soil‐only warming than the control in 2004, but was only 11% greater in 2005, while RS in the soil+air warming treatments was 31% less than the control in 2004 and 23% less in 2005. Live fine root mass (< 2 mm diameter) was less in the heated than control treatments in 2004 and statistically less (P < 0.01) in 2005. Similar root mass between the two heated treatments suggests that different heating methods (soil‐only vs. soil+air warming) can affect the rate of decomposition.  相似文献   

16.
Global climate change is expected to result in a greater frequency of extreme weather, which can cause lag effects on aboveground net primary production (ANPP). However, our understanding of lag effects is limited. To explore lag effects following extreme weather, we applied four treatments (control, doubled precipitation, 4 °C warming, and warming plus doubled precipitation) for 1 year in a randomized block design and monitored changes in ecosystem processes for 3 years in an old‐field tallgrass prairie in central Oklahoma. Biomass was estimated twice in the pretreatment year, and three times during the treatment and posttreatment years. Total plant biomass was increased by warming in spring of the treatment year and by doubled precipitation in summer. However, double precipitation suppressed fall production. During the following spring, biomass production was significantly suppressed in the formerly warmed plots 2 months after treatments ceased. Nine months after the end of treatments, fall production remained suppressed in double precipitation and warming plus double precipitation treatments. Also, the formerly warmed plots still had a significantly greater proportion of C4 plants, while the warmed plus double precipitation plots retained a high proportion of C3 plants. The lag effects of warming on biomass did not match the temporal patterns of soil nitrogen availability determined by plant root simulator probes, but coincided with warming‐induced decreases in available soil moisture in the deepest layers of soil which recovered to the pretreatment pattern approximately 10 months after the treatments ceased. Analyzing the data with an ecosystem model showed that the lagged temporal patterns of effects of warming and precipitation on biomass can be fully explained by warming‐induced differences in soil moisture. Thus, both the experimental results and modeling analysis indicate that water availability regulates lag effects of warming on biomass production.  相似文献   

17.
青藏高原高寒草甸土壤CO2排放对模拟氮沉降的早期响应   总被引:5,自引:0,他引:5  
研究大气氮沉降输入对青藏高原高寒草甸土壤-大气界面CO2交换通量的影响,对于准确评价全球变化背景下区域碳平衡至关重要。通过构建多形态、低剂量的增氮控制试验,利用静态箱-气相色谱法测定土壤CO2排放通量,同时测定相关土壤变量和地上生物量,分析高寒草甸土壤CO2排放特征及其主要驱动因子。研究结果表明:低、高剂量氮输入倾向于消耗土壤水分,而中剂量氮输入有利于土壤水分的保持;施氮初期总体上增加了土壤无机氮含量,铵态氮累积效应更为显著;施氮显著增加地上生物量和土壤CO2排放通量,铵态氮的促进效应显著高于硝态氮。另外,土壤CO2排放通量主要受土壤温度驱动,其次为地上生物量和铵态氮储量。上述结果反映了氮沉降输入短期内可能刺激了植物生长和土壤微生物活性,加剧了土壤-大气界面CO2排放。  相似文献   

18.
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   

19.
Changes in labile carbon (LC) pools and microbial communities are the primary factors controlling soil heterotrophic respiration (Rh) in warming experiments. Warming is expected to initially increase Rh but studies show this increase may not be continuous or sustained. Specifically, LC and soil microbiome have been shown to contribute to the effect of extended warming on Rh. However, their relative contribution is unclear and this gap in knowledge causes considerable uncertainty in the prediction of carbon cycle feedbacks to climate change. In this study, we used a two‐step incubation approach to reveal the relative contribution of LC limitation and soil microbial community responses in attenuating the effect that extended warming has on Rh. Soil samples from three Tibetan ecosystems—an alpine meadow (AM), alpine steppe (AS), and desert steppe (DS)—were exposed to a temperature gradient of 5–25°C. After an initial incubation period, soils were processed in one of two methods: (a) soils were sterilized then inoculated with parent soil microbes to assess the LC limitation effects, while controlling for microbial community responses; or (b) soil microbes from the incubations were used to inoculate sterilized parent soils to assess the microbial community effects, while controlling for LC limitation. We found both LC limitation and microbial community responses led to significant declines in Rh by 37% and 30%, respectively, but their relative contributions were ecosystem specific. LC limitation alone caused a greater Rh decrease for DS soils than AMs or ASs. Our study demonstrates that soil carbon loss due to Rh in Tibetan alpine soils—especially in copiotrophic soils—will be weakened by microbial community responses under short‐term warming.  相似文献   

20.
A trenching method was used to determine the contribution of root respiration to soil respiration. Soil respiration rates in a trenched plot (R trench) and in a control plot (R control) were measured from May 2000 to September 2001 by using an open-flow gas exchange system with an infrared gas analyser. The decomposition rate of dead roots (R D) was estimated by using a root-bag method to correct the soil respiration measured from the trenched plots for the additional decaying root biomass. The soil respiration rates in the control plot increased from May (240–320 mg CO2 m–2 h–1) to August (840–1150 mg CO2 m–2 h–1) and then decreased during autumn (200–650 mg CO2 m–2 h–1). The soil respiration rates in the trenched plot showed a similar pattern of seasonal change, but the rates were lower than in the control plot except during the 2 months following the trenching. Root respiration rate (R r) and heterotrophic respiration rate (R h) were estimated from R control, R trench, and R D. We estimated that the contribution of R r to total soil respiration in the growing season ranged from 27 to 71%. There was a significant relationship between R h and soil temperature, whereas R r had no significant correlation with soil temperature. The results suggest that the factors controlling the seasonal change of respiration differ between the two components of soil respiration, R r and R h.  相似文献   

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