The input of acidity to Swedish forest soils through forestry between 1955 and 2010 is compared with the acid input from atmospheric deposition. Depending on region, input of acidity from forestry was the minor part (25–45%) of the study period’s accumulated acid input but is now the dominating source (140–270 molc ha−1 year−1). The net uptake of cations due to the increase in standing forest biomass, ranged between 35 and 45% of the forestry related input of acidity while whole-tree harvesting, introduced in the late 1990s, contributed only marginally (< 2%). The geographical gradient in acid input is reflected in the proportion of acidified soils in Sweden but edaphic properties contribute to variations in acidification sensitivity. It is important to consider the acid input due to increases in standing forest biomass in acidification assessments since it is long-term and quantitatively important.Supplementary InformationThe online version contains supplementary material available at 10.1007/s13280-021-01540-y. 相似文献
Implementation of more stringent 8-hour ozone standards has led the U.S. Environmental Protection Agency to designate nonattainment
status to 474 counties nationwide, many of which had never previously violated air quality standards. As states select emission
control measures to achieve attainment in these regions, their choices pose significant implications to local economies and
the health of their citizens. Considering a case study of one such nonattainment region, Macon, Georgia, we develop a menu
of potential controls that could be implemented locally or in neighboring parts of the state. The control menu offers the
potential to control about 20–35% of ozone precursor emissions in most Georgia regions, but marginal costs increase rapidly
beyond 15–20%. We link high-order ozone sensitivities with the control menu to identify cost-optimized strategies for achieving
attainment and for alternative goals such as reducing spatially averaged or population-weighted ozone concentrations. Strategies
targeted toward attainment of Macon ozone would prioritize local reductions of nitrogen oxides, whereas controls in the more
densely populated Atlanta region are shown to be more effective for reducing statewide potential population exposure to ozone.
A U.S. EPA-sanctioned approach for demonstrating ozone attainment with photochemical models is shown to be highly dependent
on the choice of a baseline period and may not foster optimal strategies for assuring attainment and protecting human health. 相似文献
A systematic analysis of surface ozone observations in rural areas surrounding Athens is presented. The analysis is based on ozone data for the rural station Aliartos about 80 km NW of Athens center and for two stations on the northern periphery of the Athens basin: Demokritos, located 10 km NE of Athens center and Liossia, 12 km to the north. The data for these two stations are screened for cases of strong air flow from rural areas. Average hourly summer afternoon ozone mixing ratios are similar for all three stations about 60 ppb and thus exceed for the hours 12:00–20:00 LST the 55 ppb WHO guideline for human health for 8 h ozone exposure. The corresponding winter afternoon mixing ratios are at 35 ppb. However, due to the large diurnal variation, mean monthly ozone mixing ratios at Aliartos, for the months April–September vary from 32 to 40 ppb, which is comparable to the higher average ozone levels at rural stations in south-central Europe. In cases of southerly air flow in the summer in the Athens basin, afternoon ozone levels at Demokritos and Liossia are generally the highest of any in the monitoring network. Hourly average concentrations, however, are only 40% greater than rural values. A background ozone level of such magnitude will have a significant impact on estimates for the effectiveness of pollution control measures for Athens. 相似文献
An aircraft-based measurement campaign was conducted during the summer of 1996 in the vicinity of Toronto, Canada. The objective of the campaign was to assess the errors in a particular emission inventory used by three-dimensional air quality models. Measurements of NO2 and hydrocarbons were made both upwind and downwind of Toronto, on days with strong synoptic-scale flow from a west to northerly direction. The chemical composition of the background airmass on these days was typical of unpolluted continental air. Measurements have been compared with the output from an on-line air quality model (MC2-AQ) run at 5 km resolution and suggest that emissions of NOx from Toronto are well described in the emission database, though evidence that NOx emissions are underestimated for suburban regions surrounding Toronto was found. In general, no significant underestimation of hydrocarbon emissions was found, though emissions of the model propane species, which includes acetylene and benzene, was underestimated by at least a factor of two. 相似文献
In order to realistically simulate both chemistry and transport of atmospheric organic pollutants, it is indispensable that the applied models explicitly include coupling between different components of the global environment such as atmosphere, hydrosphere, cryosphere and soil system. A model with such properties is presented.
The atmospheric part of the model is based on the equations in a general contravariant form which permits easy changes of the coordinate system by redefining the metric tensor of a specifically employed coordinate system. Considering a need to include explicitly the terrain effects, the terrain following spherical coordinate system is chosen from among many possible coordinate systems. This particular system is a combination of the Gal-Chen coordinates, commonly employed in mesoscale meteorological models, and the spherical coordinates, typical for global atmospheric models.
In addition to atmospheric transport, the model also simulates the exchange between air and different types of underlying surfaces such as water, soil, snow, and ice. This approach permits a realistic representation of absorption and delayed re-emission of pollutants from the surface to the atmosphere and, consequently, allows to capture hysteresis-like effects of the exchange between the atmosphere and the other components of the system. In this model, the most comprehensive numerical representation of the exchange is that for soil. In particular, the model includes a realistic soil module which simulates both diffusion and convection of a tracer driven by evaporation from the soil, precipitation, and gravity.
The model is applied to a long-term simulation of the transport of pesticides (hexachlorocyclohexanes in particular). Emission fluxes from the soil are rigorously computed on the basis of the realistic data of the agricultural application. All four modelled systems, i.e. atmosphere, soil, hydrosphere and cryosphere, are driven by objectively analysed meteorological data supplemented, when necessary, by climatological information. Therefore, the verification against the observed data is possible. The comparison of the model results and the observations taken at remote stations in the Arctic indicates that the presented global modelling system is able to capture both trends and short-term components in the observed time series of the concentrations, and therefore, provides a useful tool for the evaluation of the source–receptor relationships. 相似文献