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1.
To assess the concern over declining base cation levels in forest soils caused by acid deposition, input-output budgets (1990s average) for sulphate (SO4), inorganic nitrogen (NO3-N; NH4-N), calcium (Ca), magnesium (Mg) and potassium (K) were synthesised for 21 forested catchments from 17 regions in Canada, the United States and Europe. Trend analysis was conducted on monthly ion concentrations in deposition and runoff when more than 9 years of data were available (14 regions, 17 sites). Annual average SO4 deposition during the 1990s ranged between 7.3 and 28.4 kg ha−1 per year, and inorganic nitrogen (N) deposition was between 2.8 and 13.8 kg ha−1 per year, of which 41–67% was nitrate (NO3-N). Over the period of record, SO4 concentration in deposition decreased in 13/14 (13 out of 14 total) regions and SO4 in runoff decreased at 14/17 catchments. In contrast, NO3-N concentrations in deposition decreased in only 1/14 regions, while NH4-N concentration patterns varied; increasing at 3/14 regions and decreasing at 2/14 regions. Nitrate concentrations in runoff decreased at 4/17 catchments and increased at only 1 site, whereas runoff levels of NH4-N increased at 5/17 catchments. Decreasing trends in deposition were also recorded for Ca, Mg, and K at many of the catchments and on an equivalent basis, accounted for up to 131% (median 22%) of the decrease in acid anion deposition. Base cation concentrations in streams generally declined over time, with significant decreases in Ca, Mg and K occurring at 8, 9 and 7 of 17 sites respectively, which accounted for up to 133% (median 48%) of the decrease in acid anion concentration. Sulphate export exceeded input at 18/21 catchments, likely due to dry deposition and/or internal sources. The majority of N in deposition (31–100%; median 94%) was retained in the catchments, although there was a tendency for greater NO3-N leaching at sites receiving higher (<7 kg ha-1 per year) bulk inorganic N deposition. Mass balance calculations show that export of Ca and Mg in runoff exceeds input at all 21 catchments, but K export only exceeds input at 16/21 sites. Estimates of base cation weathering were available for 18 sites. When included in the mass balance calculation, Ca, Mg and K exports exceeded inputs at 14, 10 and 2 sites respectively. Annual Ca and Mg losses represent appreciable proportions of the current exchangeable soil Ca and Mg pools, although losses at some of the sites likely occur from weathering reactions beneath the rooting zone and there is considerable uncertainty associated with mineral weathering estimates. Critical loads for sulphur (S) and N, using a critical base cation to aluminium ratio of 10 in soil solution, are currently exceeded at 7 of the 18 sites with base cation weathering estimates. Despite reductions in SO4 and H+ deposition, mass balance estimates indicate that acid deposition continues to acidify soils in many regions with losses of Ca and Mg of primary concern. The U.S. Government's right to retain a non-exclusive, royalty free licence in and to any copyright is acknowledged. The Canadian Crown reserves the right to retain a non-exclusive, royalty free licence in and to any copyright.  相似文献   

2.
This article takes its point of departure in two approaches to integrating climate change into Strategic Environmental Assessment (SEA): Mitigation and adaptation, and in the fact that these, as well as the synergies between them and other policy areas, are needed as part of an integrated assessment and policy response. First, the article makes a review of how positive and negative synergies between a) climate change mitigation and adaptation and b) climate change and other environmental concerns are integrated into Danish SEA practice. Then, the article discusses the implications of not addressing synergies. Finally, the article explores institutional explanations as to why synergies are not addressed in SEA practice. A document analysis of 149 Danish SEA reports shows that only one report comprises the assessment of synergies between mitigation and adaptation, whilst 9,4% of the reports assess the synergies between climate change and other environmental concerns. The consequences of separation are both the risk of trade-offs and missed opportunities for enhancing positive synergies. In order to propose explanations for the lacking integration, the institutional background is analysed and discussed, mainly based on Scott's theory of institutions. The institutional analysis highlights a regulatory element, since the assessment of climate change synergies is underpinned by legislation, but not by guidance. This means that great focus is on normative elements such as the local interpretation of legislation and of climate change mitigation and adaptation. The analysis also focuses on how the fragmentation of the organisation in which climate change and SEA are embedded has bearings on both normative and cultural-cognitive elements. This makes the assessment of synergies challenging. The evidence gathered and presented in the article points to a need for developing the SEA process and methodology in Denmark with the aim to include climate change in the assessments in a more systematic and integrated manner.  相似文献   

3.
Modelled and measured indicator species ratios of O3/NOz, O3/NOy, H2O2/HNO3, HCNO/NOy for the Lower Fraser Valley were compared with VOC-NOx-O3 sensitivity threshold values reported in previous studies. Modelled region - specific indicator ratio thresholds derived from 50% NOx and 50% VOC reduction scenarios are provided. They show strongest agreement with the H2O2/HNO3 ratio values found elsewhere. A clear transition region for the LFV from VOC to NOx sensitivity could not be identified, but there is evidence that O3 concentrations in the western valley, dominated by metropolitan Vancouver, are VOC sensitive, and the more rural eastern valley O3 concentrations exhibit greater NOx sensitivity. The UAM-V Process Analysis utility was used to identify physical and chemical mechanisms which contributed to O3 formation and destruction and indicate the key importance of entrainment from elevated layers generated by the highly complex meteorological conditions in determining near surface O3 concentrations.  相似文献   

4.
We tested whether the semi-automatic program CROCO can replace visual assessments of slides to detect changes in defoliation assessment methods. We randomly selected a series of slides of 24 Norway spruce trees with 220 field assessments made between 1986 and 1995. The slides had been randomly arranged and assessed by three experts without knowledge of the tree number or the year when the slide was taken. Defoliation scores were computed with CROCO. Each tree had thus three different defoliation scores, field assessments, photo assessments and CROCO scores.CROCO scores were less correlated with the field assessments (Spearmans rank correlation: 0.67) than were the slide assessments with the field assessments (0.79–0.83). However, CROCO was not biased against the field scores, while slide assessments systematically underestimated defoliation.In a multi-variate mixed effect model none of the variables tree overlap, tree visibility and light conditions was significant in explaining differences between slide assessors and CROCO scores. The same model applied for the differences from the field scores yielded significant effects for poor light conditions (CROCO and all assessors), for crown overlap (CROCO and one assessor) and for visibility (one assessor). We conclude, therefore, that CROCO can be used to detect past and future changes in assessment methods without bias if poor quality photographs are avoided.  相似文献   

5.
本工作从理论上分析了石灰(石)湿式洗涤法脱烟气中二氧化硫的化学原理并结合实验进行了该法的化学动力学特性、再碳酸化问题及洗涤液循环系统的研究,结果表明:净化器内洗涤温度控制在60℃以下,液气比大于40Kg/m3,洗涤液pH值控制在79的情况下,脱硫效果较佳  相似文献   

6.
Pollution vulnerability of theOwerri regional water supply aquifer wasevaluated as a basis for developing appropriateprotection strategy for the groundwaterresource. The assessment was accomplished usingLegrand, GOD, Siga and DRASTIC models.Techniques of the models generally involvedparameters rating and point count systems, whichare based on the evaluation of various parameterin relation to their capacity for enhancing orattenuating contaminants in the groundwatersystem. Field and laboratory evaluations of theparameters indicate that the Owerri areagenerally occupies a nearly, flat topographywith a relatively high groundwater recharge. Thearea is underlain by predominantly sandyfacies in the Northern area which grades intogravelly sequences towards the southwest. TheSoutheastern area is distinguished by thickclayey facies that thin westwards towards theOwerri metropolis. Effective hydraulicconductivity (Kz) in the downward directionranges from 1.44 × 10-3 to 5.6 × 10-9 m s-1; with the upper limits reflecting coarsesands and gravelly units. The amount of clay andclay-size particles in the sandy and gravellyunits is negligible, suggesting that thesorptive capacity of the units is low. Depth towater table decreases southwards while hydraulichead gradients vary between 0.09 and 0.22.Groundwater occurs in unconfined conditions inmost places except in the southeastern zonewhere it is semi-confined due to the presence ofa clayey unit. The groundwater vulnerabilitymap developed on the basis of the models andseveral other thematic maps shows that theOwerri metropolis and the southwest area ofOwerri have high vulnerability, indicatinggroundwater pollution. The existing wastedisposal sites in these sub-areas should beabandoned and rehabilitated to forstall furtherpollution of the groundwater system. Areas tothe North and Southeast of Owerri have moderateand low vulnerabilities, respectively,indicating the relatively lower sensitivity ofthe groundwater system in the sub-areas tocontamination. The lower sensitivity couldfurther be matched with properly engineeredsanitary landfills in the event of choice ofsites, as an additional protective strategy forthe groundwater system.  相似文献   

7.
Arsenic(III), selenium(IV), copper(II), lead(II), cadmium(II),zinc(II) have been determined in sea water, sediments, algae andclams by differential pulse cathodic (DPCSV) and anodic (DPASV)stripping voltammetry. The voltammetric measurements are carriedout using a conventional three-electrode cell and the ammonia-ammonium chloride buffer pH 9.2 as supporting electrolyte.The analytical procedure has been verified by the analysisof the standard reference materials (Estuarine SedimentBCR-CRM 277, Ulva Lactuca BCR-CRM 279 and Mussel Tissue BCR-CRM278). The precision and the accuracy are less than 5%. Thisprocedure is utilized for the monitoring of heavy metals inthe Po river mouth area (Italy).  相似文献   

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