微生物介导的碳氮循环过程对全球气候变化的响应

土壤是地球表层最为重要的碳库也是温室气体的源或汇。自工业革命以来,对土壤温室气体的容量、收支平衡和通量等已有较多研究和估算,但对关键过程及其源/汇的研究却十分有限。微生物是土壤碳氮转化的主要驱动者, 在生态系统碳氮循环过程中扮演重要的角色,对全球气候变化有着响应的响应、适应及反馈,然而其个体数量,群落结构和多样性如何与气候扰动相互关联、进而怎样影响生态系统过程的问题仍有待进一步探索。从微生物介导的碳氮循环过程入手,重点讨论微生物对气候变化包括温室气体(CO₂,CH₄,N₂O)增加、全球变暖、大气氮沉降等的响应和反馈,并由此提出削减温室气体排放的可能途径和今后发展的方向。     

Regionally differentiated estimates of cropland N2O emissions reduce uncertainty in global calculations

Nitrogen (N) additions to cropland soils are the largest source of anthropogenic nitrous oxide (N₂O) emissions and are an important contributor to global greenhouse gas radiative forcing. Progress in understanding controls on N₂O fluxes from soils is demonstrated in increasingly sophisticated emissions estimates with improved spatial and source resolution. These methods build upon ongoing field, laboratory, and modeling advances that are restricted to just a handful of countries. Thus, burgeoning new knowledge is of limited utility for improving N₂O emissions estimates for the rest of the world where prospects for near‐term advances are constrained by the limited breadth of observations and availability of model driver data. Here, we use Bayesian inversion to leverage information from recent national‐level N₂O emission inventories and reduce uncertainty by up to 65% for estimates of regional and global direct cropland N₂O emissions. Our estimates for the proportion of N inputs lost as N₂O vary by a factor of two between regions and depart from existing default emission factors, yet regional emissions estimates based on these factors are consistent with global, regional, and local observations. Improved regional emission factors will enhance national greenhouse gas inventories in information‐poor countries and guide efforts to reduce agricultural N₂O emissions.     

Soil GHG fluxes are altered by N deposition: New data indicate lower N stimulation of the N2O flux and greater stimulation of the calculated C pools

The effects of nitrogen (N) deposition on soil organic carbon (C) and greenhouse gas (GHG) emissions in terrestrial ecosystems are the main drivers affecting GHG budgets under global climate change. Although many studies have been conducted on this topic, we still have little understanding of how N deposition affects soil C pools and GHG budgets at the global scale. We synthesized a comprehensive dataset of 275 sites from multiple terrestrial ecosystems around the world and quantified the responses of the global soil C pool and GHG fluxes induced by N enrichment. The results showed that the soil organic C concentration and the soil CO₂, CH₄ and N₂O emissions increased by an average of 3.7%, 0.3%, 24.3% and 91.3% under N enrichment, respectively, and that the soil CH₄ uptake decreased by 6.0%. Furthermore, the percentage increase in N₂O emissions (91.3%) was two times lower than that (215%) reported by Liu and Greaver (Ecology Letters, 2009, 12:1103–1117). There was also greater stimulation of soil C pools (15.70 kg C ha^?1 year^?1 per kg N ha^?1 year^?1) than previously reported under N deposition globally. The global N deposition results showed that croplands were the largest GHG sources (calculated as CO₂ equivalents), followed by wetlands. However, forests and grasslands were two important GHG sinks. Globally, N deposition increased the terrestrial soil C sink by 6.34 Pg CO₂/year. It also increased net soil GHG emissions by 10.20 Pg CO₂‐Geq (CO₂ equivalents)/year. Therefore, N deposition not only increased the size of the soil C pool but also increased global GHG emissions, as calculated by the global warming potential approach.     

Nitrous oxide emissions from inland waters: Are IPCC estimates too high?

Nitrous oxide (N₂O) emissions from inland waters remain a major source of uncertainty in global greenhouse gas budgets. N₂O emissions are typically estimated using emission factors (EFs), defined as the proportion of the terrestrial nitrogen (N) load to a water body that is emitted as N₂O to the atmosphere. The Intergovernmental Panel on Climate Change (IPCC) has proposed EFs of 0.25% and 0.75%, though studies have suggested that both these values are either too high or too low. In this work, we develop a mechanistic modeling approach to explicitly predict N₂O production and emissions via nitrification and denitrification in rivers, reservoirs and estuaries. In particular, we introduce a water residence time dependence, which kinetically limits the extent of denitrification and nitrification in water bodies. We revise existing spatially explicit estimates of N loads to inland waters to predict both lumped watershed and half‐degree grid cell emissions and EFs worldwide, as well as the proportions of these emissions that originate from denitrification and nitrification. We estimate global inland water N₂O emissions of 10.6–19.8 Gmol N year^?1 (148–277 Gg N year^?1), with reservoirs producing most N₂O per unit area. Our results indicate that IPCC EFs are likely overestimated by up to an order of magnitude, and that achieving the magnitude of the IPCC's EFs is kinetically improbable in most river systems. Denitrification represents the major pathway of N₂O production in river systems, whereas nitrification dominates production in reservoirs and estuaries.     

Denitrification Potential and CO2 Emission in the Northern Forest Soils of the Yenisei Meridian (the Siberian IGBP Transect)

To estimate the probable contribution of northern forest soils to the global budget of greenhouse microgases, the cryogenic soils along the Yenisei meridian have been studied with respect to their potential denitrification and carbon mineralization activities. It is shown that the forest soils of the boreal zone have a high denitrification potential and, under conditions of a high nitrate nitrogen content, may be a source of nitrous oxide emission. A significant correlation is observed between N₂O and CO₂ emissions (r = 0.85, p < 0.001).     

Global soil nitrous oxide emissions since the preindustrial era estimated by an ensemble of terrestrial biosphere models: Magnitude,attribution, and uncertainty

Our understanding and quantification of global soil nitrous oxide (N₂O) emissions and the underlying processes remain largely uncertain. Here, we assessed the effects of multiple anthropogenic and natural factors, including nitrogen fertilizer (N) application, atmospheric N deposition, manure N application, land cover change, climate change, and rising atmospheric CO₂ concentration, on global soil N₂O emissions for the period 1861–2016 using a standard simulation protocol with seven process‐based terrestrial biosphere models. Results suggest global soil N₂O emissions have increased from 6.3 ± 1.1 Tg N₂O‐N/year in the preindustrial period (the 1860s) to 10.0 ± 2.0 Tg N₂O‐N/year in the recent decade (2007–2016). Cropland soil emissions increased from 0.3 Tg N₂O‐N/year to 3.3 Tg N₂O‐N/year over the same period, accounting for 82% of the total increase. Regionally, China, South Asia, and Southeast Asia underwent rapid increases in cropland N₂O emissions since the 1970s. However, US cropland N₂O emissions had been relatively flat in magnitude since the 1980s, and EU cropland N₂O emissions appear to have decreased by 14%. Soil N₂O emissions from predominantly natural ecosystems accounted for 67% of the global soil emissions in the recent decade but showed only a relatively small increase of 0.7 ± 0.5 Tg N₂O‐N/year (11%) since the 1860s. In the recent decade, N fertilizer application, N deposition, manure N application, and climate change contributed 54%, 26%, 15%, and 24%, respectively, to the total increase. Rising atmospheric CO₂ concentration reduced soil N₂O emissions by 10% through the enhanced plant N uptake, while land cover change played a minor role. Our estimation here does not account for indirect emissions from soils and the directed emissions from excreta of grazing livestock. To address uncertainties in estimating regional and global soil N₂O emissions, this study recommends several critical strategies for improving the process‐based simulations.     

Methane and nitrous oxide emissions from rice paddy fields as affected by nitrogen fertilisers and water management

Methane and N₂O emissions affected by nitrogen fertilisers were measured simultaneously in rice paddy fields under intermittent irrigation in 1994. Ammonium sulphate and urea were applied at rates of 0 (control), 100 and 300 kg N ha^-1. The results showed that CH₄ emission, on the average, decreased by 42 and 60% in the ammonium sulphate treatments and 7 and 14% in the urea treatments at rates of 100 and 300 kg N ha^-1, respectively, compared to the control. N₂O emission increased significantly with the increase in the nitrogen application rate. N₂O emission was higher from ammonium sulphate treatments than from the urea treatments at the same application rate. A trade-off effect between CH₄ and N₂O emission was clearly observed. The N₂O flux was very small when the rice paddy plots were flooded, but peaked at the beginning of the disappearance of floodwater. In contrast, the CH₄ flux peaked during flooding and was significantly depressed by mid-season aeration (MSA). The results suggest that it is important to evaluate the integrative effects of water management and fertiliser application for mitigating greenhouse gas emissions in order to attenuate the greenhouse effect contributed by rice paddy fields.     

Soil CN ratio as a scalar parameter to predict nitrous oxide emissions

Forested histosols have been found in some cases to be major, and in other cases minor, sources of the greenhouse gas nitrous oxide (N₂O). In order to estimate the total national or global emissions of N₂O from histosols, scaling or mapping parameters that can separate low‐ and high‐emitting sites are needed, and should be included in soil databases. Based on interannual measurements of N₂O emissions from drained forested histosols in Sweden, we found a strong negative relationship between N₂O emissions and soil CN ratios (r²_adj=0.96, mean annual N₂O emission=ae^{(?b CN ratio)}). The same equation could be used to estimate the N₂O emissions from Finnish and German sites based on CN ratios in published data. We envisage that the correlation between N₂O emissions and CN ratios could be used to scale N₂O emissions from histosols determined at sampled sites to national levels. However, at low CN ratios (i.e. below 15–20) other parameters such as climate, pH and groundwater tables increase in importance as regulating factors affecting N₂O emissions.     

中国农业系统近40年温室气体排放核算

基于排放因子法构建了包含种植业和牲畜养殖业的农业系统温室气体排放核算体系,系统核算了1980-2020年我国全国尺度上的农业系统温室气体排放总量和变化趋势,并在区县级尺度下对1980、2000、2011年的中国农业系统的温室气体排放量进行核算,对比不同阶段农业系统温室气体排放变化的时空异质性规律。研究发现：1980-2020年我国农业系统温室气体排放量呈波动增长趋势,增长了近46%。CH₄是农业系统排放贡献最大的温室气体,占总排放量的47.33%。我国农业系统温室气体排放与不同地区农业生产方式有关,CH₄排放量高的地区主要位于我国主要水稻产区以及旱地作物产区。CO₂排放量高的地区主要位于东北、西北等地区以及华东地区。N₂O排放量较高地区主要位于西北的主要畜牧养殖地区,以及我国农业经济发展水平高的中南部地区。研究有助于揭示我国农业温室气体排放的动态特征,现状规律,以及空间差异性特征,从农业减排角度为实现双碳目标提供科学参考。     

Mitigation of ammonia,nitrous oxide and methane emissions from manure management chains: a meta‐analysis and integrated assessment

Livestock manure contributes considerably to global emissions of ammonia (NH₃) and greenhouse gases (GHG), especially methane (CH₄) and nitrous oxide (N₂O). Various measures have been developed to mitigate these emissions, but most of these focus on one specific gas and/or emission source. Here, we present a meta‐analysis and integrated assessment of the effects of mitigation measures on NH₃, CH₄ and (direct and indirect) N₂O emissions from the whole manure management chain. We analysed the effects of mitigation technologies on NH₃, CH₄ and N₂O emissions from individual sources statistically using results of 126 published studies. Whole‐chain effects on NH₃ and GHG emissions were assessed through scenario analysis. Significant NH₃ reduction efficiencies were observed for (i) housing via lowering the dietary crude protein (CP) content (24–65%, compared to the reference situation), for (ii) external slurry storages via acidification (83%) and covers of straw (78%) or artificial films (98%), for (iii) solid manure storages via compaction and covering (61%, compared to composting), and for (iv) manure application through band spreading (55%, compared to surface application), incorporation (70%) and injection (80%). Acidification decreased CH₄ emissions from stored slurry by 87%. Significant increases in N₂O emissions were found for straw‐covered slurry storages (by two orders of magnitude) and manure injection (by 26–199%). These side‐effects of straw covers and slurry injection on N₂O emission were relatively small when considering the total GHG emissions from the manure chain. Lowering the CP content of feed and acidifying slurry are strategies that consistently reduce NH₃ and GHG emissions in the whole chain. Other strategies may reduce emissions of a specific gas or emissions source, by which there is a risk of unwanted trade‐offs in the manure management chain. Proper farm‐scale combinations of mitigation measures are important to minimize impacts of livestock production on global emissions of NH₃ and GHG.     

A hybrid approach to identify the risk priority of sources of greenhouse gases

Abstract

Examination of greenhouse gas emissions is crucial for understanding the global warming. For this reason, identification of the sources of greenhouse gas emissions is crucial. This paper presents a hybrid multi criteria decision making method, which combines analytic hierarchy process and technique for order preference by similarity to ideal solution and compares this method with actual data for identifying the risk priority of sources of greenhouse gas emissions. For this purpose, the historical data of 25-years, for six-greenhouse gas sources and three-greenhouse gases (CO₂, CH_4, N₂O) are considered. Consequently, it was found that while incineration of wastes caused the minimum GHG emissions, energy sector caused the maximum GHG emissions. The results of this paper show that use of this hybrid method is easy and intelligible, and has a good potential for sorting the risk priority of sources of greenhouse gas emissions.     

模拟氮沉降对马尾松土壤微生物群落结构及温室气体释放的影响

以2年生马尾松(Pinus massoniana)盆栽苗土壤为对象,通过施氮肥模拟氮沉降对土壤理化性质、微生物群落结构及温室气体释放的影响,探明氮沉降对森林土壤温室气体释放的驱动机制。结果表明,模拟氮沉降处理显著提高了土壤速效氮含量和苗木根系氮含量;土壤微生物碳(SMBC)含量比对照显著下降78%,而土壤微生物氮(SMBN)则提高2.6倍。模拟氮沉降处理显著降低土壤中微生物群落总含量。施氮肥对马尾松土壤N_2O和CO_2的释放速率均有显著影响,增施氮肥不仅显著提高了土壤N_2O的释放速率,而且CO_2释放速率短期内也显著提高,但伴随微生物群落的下降,施肥后期CO_2释放速率表现下降趋势。相关分析表明,土壤CO_2和N_2O释放与土壤pH值、土壤温度、土壤湿度、土壤速效氮含量及SMBC、SMBN相关;逐步回归分析表明,土壤硝态氮含量的变化是驱动土壤温室气体释放的主导因子。3株种植单位土壤体积内根系生物量较高,增加了土壤水分的消耗速率和氮的吸收固定,因而减少N_2O的释放速率。以上研究阐明了氮沉降或过量施肥对土壤氮含量、土壤pH值、根系生物量及氮含量、土壤微生物群落结构等因子的影响,这些因子直接或间接影响土壤温室气体释放速率。氮沉降及施用氮肥是加快土壤温室气体(CO_2和N_2O)排放进程的重要因素。     

Modeling nitrous oxide emission from rivers: a global assessment

Estimates of global riverine nitrous oxide (N₂O) emissions contain great uncertainty. We conducted a meta‐analysis incorporating 169 observations from published literature to estimate global riverine N₂O emission rates and emission factors. Riverine N₂O flux was significantly correlated with NH₄, NO₃ and DIN (NH₄ + NO₃) concentrations, loads and yields. The emission factors EF(a) (i.e., the ratio of N₂O emission rate and DIN load) and EF(b) (i.e., the ratio of N₂O and DIN concentrations) values were comparable and showed negative correlations with nitrogen concentration, load and yield and water discharge, but positive correlations with the dissolved organic carbon : DIN ratio. After individually evaluating 82 potential regression models based on EF(a) or EF(b) for global, temperate zone and subtropical zone datasets, a power function of DIN yield multiplied by watershed area was determined to provide the best fit between modeled and observed riverine N₂O emission rates (EF(a): R² = 0.92 for both global and climatic zone models, n = 70; EF(b): R² = 0.91 for global model and R² = 0.90 for climatic zone models, n = 70). Using recent estimates of DIN loads for 6400 rivers, models estimated global riverine N₂O emission rates of 29.6–35.3 (mean = 32.2) Gg N₂O–N yr⁻¹ and emission factors of 0.16–0.19% (mean = 0.17%). Global riverine N₂O emission rates are forecasted to increase by 35%, 25%, 18% and 3% in 2050 compared to the 2000s under the Millennium Ecosystem Assessment's Global Orchestration, Order from Strength, Technogarden, and Adapting Mosaic scenarios, respectively. Previous studies may overestimate global riverine N₂O emission rates (300–2100 Gg N₂O–N yr⁻¹) because they ignore declining emission factor values with increasing nitrogen levels and channel size, as well as neglect differences in emission factors corresponding to different nitrogen forms. Riverine N₂O emission estimates will be further enhanced through refining emission factor estimates, extending measurements longitudinally along entire river networks and improving estimates of global riverine nitrogen loads.     

The global nitrogen cycle in the twenty-first century

Global nitrogen fixation contributes 413 Tg of reactive nitrogen (N_r) to terrestrial and marine ecosystems annually of which anthropogenic activities are responsible for half, 210 Tg N. The majority of the transformations of anthropogenic N_r are on land (240 Tg N yr⁻¹) within soils and vegetation where reduced N_r contributes most of the input through the use of fertilizer nitrogen in agriculture. Leakages from the use of fertilizer N_r contribute to nitrate (NO₃⁻) in drainage waters from agricultural land and emissions of trace N_r compounds to the atmosphere. Emissions, mainly of ammonia (NH₃) from land together with combustion related emissions of nitrogen oxides (NO_x), contribute 100 Tg N yr⁻¹ to the atmosphere, which are transported between countries and processed within the atmosphere, generating secondary pollutants, including ozone and other photochemical oxidants and aerosols, especially ammonium nitrate (NH₄NO₃) and ammonium sulfate (NH₄)₂SO₄. Leaching and riverine transport of NO₃ contribute 40–70 Tg N yr⁻¹ to coastal waters and the open ocean, which together with the 30 Tg input to oceans from atmospheric deposition combine with marine biological nitrogen fixation (140 Tg N yr⁻¹) to double the ocean processing of N_r. Some of the marine N_r is buried in sediments, the remainder being denitrified back to the atmosphere as N₂ or N₂O. The marine processing is of a similar magnitude to that in terrestrial soils and vegetation, but has a larger fraction of natural origin. The lifetime of N_r in the atmosphere, with the exception of N₂O, is only a few weeks, while in terrestrial ecosystems, with the exception of peatlands (where it can be 10²–10³ years), the lifetime is a few decades. In the ocean, the lifetime of N_r is less well known but seems to be longer than in terrestrial ecosystems and may represent an important long-term source of N₂O that will respond very slowly to control measures on the sources of N_r from which it is produced.     

Spatially explicit estimates of N2O emissions from croplands suggest climate mitigation opportunities from improved fertilizer management

With increasing nitrogen (N) application to croplands required to support growing food demand, mitigating N₂O emissions from agricultural soils is a global challenge. National greenhouse gas emissions accounting typically estimates N₂O emissions at the country scale by aggregating all crops, under the assumption that N₂O emissions are linearly related to N application. However, field studies and meta‐analyses indicate a nonlinear relationship, in which N₂O emissions are relatively greater at higher N application rates. Here, we apply a super‐linear emissions response model to crop‐specific, spatially explicit synthetic N fertilizer and manure N inputs to provide subnational accounting of global N₂O emissions from croplands. We estimate 0.66 Tg of N₂O‐N direct global emissions circa 2000, with 50% of emissions concentrated in 13% of harvested area. Compared to estimates from the IPCC Tier 1 linear model, our updated N₂O emissions range from 20% to 40% lower throughout sub‐Saharan Africa and Eastern Europe, to >120% greater in some Western European countries. At low N application rates, the weak nonlinear response of N₂O emissions suggests that relatively large increases in N fertilizer application would generate relatively small increases in N₂O emissions. As aggregated fertilizer data generate underestimation bias in nonlinear models, high‐resolution N application data are critical to support accurate N₂O emissions estimates.     

Bioethanol production from sugarcane and emissions of greenhouse gases – known and unknowns

Bioethanol production from sugarcane is discussed as an alternative energy source to reduce dependencies of regional economies on fossil fuels. Even though bioethanol production from sugarcane is considered to be a beneficial and cost‐effective greenhouse gas (GHG) mitigation strategy, it is still a matter of controversy due to insufficient information on the total GHG balance of this system. Aside from the necessity to account for the impact of land use change (LUC), soil N₂O emissions during sugarcane production and emissions of GHG due to preharvest burning may significantly impact the GHG balance. Based on a thorough literature review, we show that direct N₂O emissions from sugarcane fields due to nitrogen (N) fertilization result in an emission factor of 3.87±1.16% which is much higher than suggested by IPCC (1%). N₂O emissions from N fertilization accounted for 40% of the total GHG emissions from ethanol–sugarcane production, with an additional 17% from trash burning. If LUC‐related GHG emissions are considered, the total GHG balance turns negative mainly due to vegetation carbon losses. Our study also shows that major gaps in knowledge still exist about GHG sources related to agricultural management during sugarcane production, e.g. effects of irrigation, vinasse and filter cake application. Therefore, more studies are needed to assess if bioethanol from sugarcane is a viable option to reduce energy‐related GHG emissions.     

Exchange of gaseous nitrogen compounds between agricultural systems and the atmosphere

Crop and livestock agricultural production systems are important contributors to local, regional and global budgets of NH₃, NO_x (NO + NO₂) and N₂O. Emissions of NH₃ and NO_x (which are biologically and chemically active) into the atmosphere serve to redistribute fixed N to local and regional aquatic and terrestrial ecosystems that may otherwise be disconnected from the sources of the N gases. The emissions of NO_x also contribute to local elevated ozone concentrations while N₂O emissions contribute to global greenhouse gas accumulation and to stratospheric ozone depletion.Ammonia is the major gaseous base in the atmosphere and serves to neutralize about 30% of the hydrogen ions in the atmosphere. Fifty to 75% of the 55 Tg N yr^–1 NH₃ from terrestrial systems is emitted from animal and crop-based agriculture from animal excreta and synthetic fertilizer application. About half of the 50 Tg N yr^–1 of NO_x emitted from the earth surface annually arises from fossil fuel combustion and the remainder from biomass burning and emissions from soil. The NO_x emitted, principally as nitric oxide (NO), reacts rapidly in the atmosphere and in a complex cycle with light, ozone and hydrocarbons, and produces nitric acid and particulate nitrate. These materials can interact with plants and the soil locally or be transported form the site and interact with atmospheric particulate to form aerosols. These salts and aerosols return to fertilize terrestrial and aquatic systems in wet and dry deposition. A small fraction of this N may be biologically converted to N₂O. About 5% of the total atmospheric greenhouse effect is attributed to N₂O from which 70% of the annual global anthropogenic emissions come from animal and crop production.The coupling of increased population with a move of a large sector of the world population to diets that require more energy and N input, will lead to continued increases in anthropogenic input into the global N cycle. This scenario suggests that emissions of NH₃, NO_x and N₂O from agricultural systems will continue to increase and impact global terrestrial and aquatic systems, even those far removed from agricultural production, to an ever growing extent, unless N resources are used more efficiently or food consumption trends change.     

Gaseous nitrogen emmissions from undisturbed terrestrial ecosystems: An assessment of their impacts on local and global nitrogen budgets

There is increasing interest in the importance of nitrogen gas emissions from natural (non-agricultural) ecosystems with respect to local as well as global nitrogen budgets and with respect to the effects of nitrogen oxides on atmospheric ozone levels and global warming. The volatile forms of nitrogen of common interest are ammonia (NH₃), nitrous oxide, (N₂O), dinitrogen (N₂), and NO_x (principally NO + NO₂). It is often difficult to attribute emissions of these compounds from soils to a single process because they are produced by a variety of common biogeochemical mechanisms. Although environmental conditions in the soil often appear to favor nitrogen gas emissions, the potential nitrogen gas emission rate from undisturbed ecosystems is rarely approached. The best estimates to date suggest that nitrogen gas emission rates from undisturbed ecosystems typically range from > 1 to perhaps 10 or 20 kg N ha^-1 yr^-1. Under certain conditions, however, emission rates may be much higher. For example, excreta from animals in grasslands may elevate ammonia volatilization up to 100 kg N ha^-1 yr^-1 depending on grazer density; tidal input of nutrients to coastal wetlands may support denitrification rates of several hundred kg N ha^-1 yr^-1 . Excepting such cases, gaseous nitrogen losses are probably a small component of the local nitrogen budget in most undisturbed ecosystems. However, emissions from undisturbed soils are an important component of the global source strengths for (N₂O + N₂), N₂O and NO_x (50%, 21%, and 10% respectively). Emission rates of N₂O from natural ecosystems are higher than assumed previously by perhaps 10 times. Large-scale disturbance may have a stimulatory effect on nitrogen emission rates which could have important effects on global nitrogen budgets. There is a need for more sophisticated methods to account for natural temporal and spatial variations of emissions rates, to more accurately and precisely assess their global source strengths.     

模拟氮沉降对藏北高寒草甸温室气体排放的影响

目前,高寒草甸对全球温室效应的贡献仍具有不确定性,而随着N沉降的增加,该系统温室体气排放也必将发生变化。为揭示高寒草甸对N沉降的响应机制,探讨其对全球变化的反馈作用,利用人工添加氮素的方法,于2014年生长季(6-9月)在那曲地区那曲县设置不同水平N添加梯度(0、7、20kg hm~(-2)a~(-1)和40 kg hm~(-2)a~(-1)),模拟氮沉降增加对藏北高寒草甸温室气体排放的影响。经过1a的研究结果表明:1)施氮显著促进了CO_2排放但对CH_4的吸收和N_2O的排放无显著影响。总体而言,添加氮素明显增加了温室气体排放总量,其中N2O处理下高寒草甸温室气体排放总量最高。2)回归分析结果表明,CO_2与NPP(总生物量)和TOC(土壤有机碳)线性相关(P0.05),而与TN(总氮)、NH_4~+-N和NO_3~--N均无显著相关关系(P0.05),CH_4与TN/NPP/TOC/NH_4~+-N/NO_3~--N均不相关(P0.05),N_2O与NPP/TOC/NO_3~--N均显著线性相关(P0.05),而与TN/NH_4~+-N不相关。综合初步研究结果,未来氮沉降增加条件下,藏北高寒草甸温室气体排放通量将有可能明显增加,从而对气候变化产生重要的反馈作用。