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Overviewing the European carbon (C), greenhouse gas (GHG), and non‐GHG fluxes, gross primary productivity (GPP) is about 9.3 Pg yr?1, and fossil fuel imports are 1.6 Pg yr?1. GPP is about 1.25% of solar radiation, containing about 360 × 1018 J energy – five times the energy content of annual fossil fuel use. Net primary production (NPP) is 50%, terrestrial net biome productivity, NBP, 3%, and the net GHG balance, NGB, 0.3% of GPP. Human harvest uses 20% of NPP or 10% of GPP, or alternatively 1‰ of solar radiation after accounting for the inherent cost of agriculture and forestry, for production of pesticides and fertilizer, the return of organic fertilizer, and for the C equivalent cost of GHG emissions. C equivalents are defined on a global warming potential with a 100‐year time horizon. The equivalent of about 2.4% of the mineral fertilizer input is emitted as N2O. Agricultural emissions to the atmosphere are about 40% of total methane, 60% of total NO‐N, 70% of total N2O‐N, and 95% of total NH3‐N emissions of Europe. European soils are a net C sink (114 Tg yr?1), but considering the emissions of GHGs, soils are a source of about 26 Tg CO2 C‐equivalent yr?1. Forest, grassland and sediment C sinks are offset by GHG emissions from croplands, peatlands and inland waters. Non‐GHGs (NH3, NOx) interact significantly with the GHG and the C cycle through ammonium nitrate aerosols and dry deposition. Wet deposition of nitrogen (N) supports about 50% of forest timber growth. Land use change is regionally important. The absolute flux values total about 50 Tg C yr?1. Nevertheless, for the European trace‐gas balance, land‐use intensity is more important than land‐use change. This study shows that emissions of GHGs and non‐GHGs significantly distort the C cycle and eliminate apparent C sinks.  相似文献   
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This paper examines long‐term eddy covariance data from 18 European and 17 North American and Asian forest, wetland, tundra, grassland, and cropland sites under non‐water‐stressed conditions with an empirical rectangular hyperbolic light response model and a single layer two light‐class carboxylase‐based model. Relationships according to ecosystem functional type are demonstrated between empirical and physiological parameters, suggesting linkages between easily estimated parameters and those with greater potential for process interpretation. Relatively sparse documentation of leaf area index dynamics at flux tower sites is found to be a major difficulty in model inversion and flux interpretation. Therefore, a simplification of the physiological model is carried out for a subset of European network sites with extensive ancillary data. The results from these selected sites are used to derive a new parameter and means for comparing empirical and physiologically based methods across all sites, regardless of ancillary data. The results from the European analysis are then compared with results from the other Northern Hemisphere sites and similar relationships for the simplified process‐based parameter were found to hold for European, North American, and Asian temperate and boreal climate zones. This parameter is useful for bridging between flux network observations and continental scale spatial simulations of vegetation/atmosphere carbon dioxide exchange.  相似文献   
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