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Atmospheric deposition of nitrogen (N) and phosphorus (P) far exceeding the pre-industrial levels have the potential to change carbon (C) dynamics in northern peatlands. However, the responses of soil C concentration and organo-chemical composition to different rates and durations of nutrient enrichment are still unclear. Here, we compared the short- (3 years) and long-term (10 years) effects of N and P fertilizations on the physicochemical properties of peat and porewater in a bog-fen complex in northern China. Our results showed that the short-term fertilization increased Sphagnum moss cover, while the expansion of vascular plants was observed owing to the long-term fertilization. The preserved soil C did not vary considerably after the short- and long-term fertilizations. The harsh soil conditions may impede the decomposition of organic matters by soil microorganisms during the short-term fertilization. For the long-term fertilization, the input of high-phenolic litters owing to vascular plant expansion likely exerted an important control on soil C dynamics. These processes constrained the variation in soil C concentrations when the addition rate and cumulative amount of external N and P increased, which will advance our understanding and prediction of the resilience of soil C storage to imbalanced nutrient enrichment of N and P in northern peatlands.
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Atmospheric deposition of nitrogen (N) and phosphorus (P) far exceeding the pre-industrial levels have the potential to change carbon (C) dynamics in northern peatlands. However, the responses of soil C concentration and organo-chemical composition to different rates and durations of nutrient enrichment are still unclear. Here, we compared the short- (3 years) and long-term (10 years) effects of N and P fertilizations on the physicochemical properties of peat and porewater in a bog-fen complex in northern China. Our results showed that the short-term fertilization increased Sphagnum moss cover, while the expansion of vascular plants was observed owing to the long-term fertilization. The preserved soil C did not vary considerably after the short- and long-term fertilizations. The harsh soil conditions may impede the decomposition of organic matters by soil microorganisms during the short-term fertilization. For the long-term fertilization, the input of high-phenolic litters owing to vascular plant expansion likely exerted an important control on soil C dynamics. These processes constrained the variation in soil C concentrations when the addition rate and cumulative amount of external N and P increased, which will advance our understanding and prediction of the resilience of soil C storage to imbalanced nutrient enrichment of N and P in northern peatlands.
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Abstract Background Changes in foliar nitrogen (N) and phosphorus (P) stoichiometry play important roles in predicting the effects of global change on ecosystem structure and function. However, there is substantial debate on the effects of P addition on foliar N and P stoichiometry, particularly under different levels of N addition. Thus, we conducted a global meta-analysis to investigate how N addition alters the effects of P addition on foliar N and P stoichiometry across different rates and durations of P addition and plant growth types based on more than 1150 observations. Results We found that P addition without N addition increased foliar N concentrations, whereas P addition with N addition had no effect. The positive effects of P addition on foliar P concentrations were greater without N addition than with N addition. Additionally, the effects of P addition on foliar N, P and N:P ratios varied with the rate and duration of P addition. In particular, short-term or low-dose P addition with and without N addition increased foliar N concentration, and the positive effects of short-term or low-dose P addition on foliar P concentrations were greater without N addition than with N addition. The responses of foliar N and P stoichiometry of evergreen plants to P addition were greater without N addition than with N addition. Moreover, regardless of N addition, soil P availability was more effective than P resorption efficiency in predicting the changes in foliar N and P stoichiometry in response to P addition. Conclusions Our results highlight that increasing N deposition might alter the response of foliar N and P stoichiometry to P addition and demonstrate the important effect of the experimental environment on the results. These results advance our understanding of the response of plant nutrient use efficiency to P addition with increasing N deposition.
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Abstract Both anthropogenic activities and climate change can affect the biogeochemical processes of natural wetland methanogenesis. Quantifying possible impacts of changing climate and wetland area on wetland methane (CH 4 ) emissions in China is important for improving our knowledge on CH 4 budgets locally and globally. However, their respective and combined effects are uncertain. We incorporated changes in wetland area derived from remote sensing into a dynamic CH 4 model to quantify the human and climate change induced contributions to natural wetland CH 4 emissions in China over the past three decades. Here we found that human-induced wetland loss contributed 34.3% to the CH 4 emissions reduction (0.92 TgCH 4 ), and climate change contributed 20.4% to the CH 4 emissions increase (0.31 TgCH 4 ), suggesting that decreasing CH 4 emissions due to human-induced wetland reductions has offset the increasing climate-driven CH 4 emissions. With climate change only, temperature was a dominant controlling factor for wetland CH 4 emissions in the northeast (high latitude) and Qinghai-Tibet Plateau (high altitude) regions, whereas precipitation had a considerable influence in relative arid north China. The inevitable uncertainties caused by the asynchronous for different regions or periods due to inter-annual or seasonal variations among remote sensing images should be considered in the wetland CH 4 emissions estimation.
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Abstract With over one‐third of terrestrial net primary productivity transferring to the litter layer annually, the carbon release from litter serves as a crucial valve in atmospheric carbon dioxide concentrations. However, few quantitative global projections of litter carbon release rate in response to climate change exist. Here, we combined a global foliar litter carbon release dataset (8973 samples) to generate spatially explicitly estimates of the response of their residence time ( τ ) to climate change. Results show a global mean litter carbon release rate () of 0.69 year −1 (ranging from 0.09–5.6 year −1 ). Under future climate scenarios, global mean τ is projected to decrease by a mean of 2.7% (SSP 1–2.6) and 5.9% (SSP 5–8.5) during 2071–2100 period. Locally, the alleviation of temperature and moisture restrictions corresponded to obvious decreases in τ in cold and arid regions, respectively. In contract, τ in tropical humid broadleaf forests increased by 4.6% under SSP 5–8.5. Our findings highlight the vegetation type as a powerful proxy for explaining global patterns in foliar litter carbon release rates and the role of climate conditions in predicting responses of carbon release to climate change. Our observation‐based estimates could refine carbon cycle parameterization, improving projections of carbon cycle–climate feedbacks.
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Abstract Terrestrial ecosystems carbon and water cycles are tightly coupled through photosynthesis and evapotranspiration processes. The ratios of carbon stored to carbon uptake and water loss to carbon gain are key ecophysiological indicators essential to assess the magnitude and response of the terrestrial plant to the changing climate. Here, we use estimates from 10 terrestrial ecosystem models to quantify the impacts of climate, atmospheric CO 2 concentration, and nitrogen (N) deposition on water use efficiency (WUE), and carbon use efficiency (CUE). We find that across models, WUE increases over the 20 th Century particularly due to CO 2 fertilization and N deposition and compares favorably to experimental studies. Also, the results show a decrease in WUE with climate for the last 3 decades, in contrasts with up-scaled flux observations that demonstrate a constant WUE. Modeled WUE responds minimally to climate with modeled CUE exhibiting no clear trend across space and time. The divergence between simulated and observationally-constrained WUE and CUE is driven by modeled NPP and autotrophic respiration, nitrogen cycle, carbon allocation, and soil moisture dynamics in current ecosystem models. We suggest that carbon-modeling community needs to reexamine stomatal conductance schemes and the soil-vegetation interactions for more robust modeling of carbon and water cycles.
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Abstract Methane (CH 4 ) emissions from tropical wetlands contribute 60%–80% of global natural wetland CH 4 emissions. Decreased wetland CH 4 emissions can act as a negative feedback mechanism for future climate warming and vice versa. The impact of the El Niño–Southern Oscillation (ENSO) on CH 4 emissions from wetlands remains poorly quantified at both regional and global scales, and El Niño events are expected to become more severe based on climate models’ projections. We use a process‐based model of global wetland CH 4 emissions to investigate the impacts of the ENSO on CH 4 emissions in tropical wetlands for the period from 1950 to 2012. The results show that CH 4 emissions from tropical wetlands respond strongly to repeated ENSO events, with negative anomalies occurring during El Niño periods and with positive anomalies occurring during La Niña periods. An approximately 8‐month time lag was detected between tropical wetland CH 4 emissions and ENSO events, which was caused by the combined time lag effects of ENSO events on precipitation and temperature over tropical wetlands. The ENSO can explain 49% of interannual variations for tropical wetland CH 4 emissions. Furthermore, relative to neutral years, changes in temperature have much stronger effects on tropical wetland CH 4 emissions than the changes in precipitation during ENSO periods. The occurrence of several El Niño events contributed to a lower decadal mean growth rate in atmospheric CH 4 concentrations throughout the 1980s and 1990s and to stable atmospheric CH 4 concentrations from 1999 to 2006, resulting in negative feedback to global warming.