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51.
Hauke Von Seht 《Local Environment》2013,18(1):23-34
Local environmental policies are sometimes seen as standing in the way of socio-economic progress. Against the background of these concerns, the actual socio-economic impacts of climate protection measures are discussed in this paper. It is structured as follows. First, the concept of primary and secondary effects of climate policies is introduced. Secondly, there is a discussion of financial and economic impacts of local climate policies. Finally, information is given on the consequences of such measures for local energy security and air quality. The main conclusion is that, at least in the field of climate policies, there is a huge potential for local measures that are socioeconomically attractive to local communities. HAUKE VON SEHT, Impactos socio-económicos de políticas del medio ambiente local, un análisis para el campo de protección climática . Las políticas ambientales locales son vistas algunas veces como si estuvieran en la via del progreso socio-económico. En contra de los antecedentes de estos asuntos, los impactos socio-económicos actuales de las medidas de protección climaticas son discutidos en este documento. Está extructurado de la siguiente manera: Primero serán introducidos el concepto de efectos primarios y secundarios de las políticas climáticas. Luego sigue una discusión de impactos económicos y financieros de las políticas climáticas locales, seguido por información de las consecuencias de tales medidas para la calidad del aire y seguridad de energía local. La conclusión principal es que por lo menos en el campo de las políticas climáticas hay un inmenso potencial de medidas locales que son socio-económicamente actractivas a las comunidades locales. 相似文献
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53.
Nemli G Demirel S Gümüşkaya E Aslan M Acar C 《Waste management (New York, N.Y.)》2009,29(3):1129-1131
This study investigated some of the important physical (thickness swelling) and mechanical (modulus of rupture, modulus of elasticity and internal bond) properties of single-layer particleboard panels made from eucalyptus (Eucalyptus camaldulensis Dehn.), waste of grass clippings (Lolium perenne L.) and combinations of the two. The chemical properties (pH, holocelluse and alpha cellulose contents, and water, alcohol-benzene and 1% sodium hydroxide solubilities) of the raw materials were also determined. Panels with a 6:94 ratio of grass-to-eucalyptus particles had the required mechanical properties for interior fitments including furniture and general uses. Boards manufactured with 100% grass clippings exhibited the lowest quality. The overall panel properties improved with a lower percentage of grass clippings added. Based on initial results, it also appears that grass should compose no more than 13% to achieve acceptable panel properties for interior fitments and general uses. 相似文献
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56.
Skyllberg U Drott A Lambertsson L Björn E Karlsson T Johnson T Heinemo SA Holmström H 《Ambio》2007,36(6):437-442
Sediments contaminated by various sources of mercury (Hg) were studied at 8 sites in Sweden covering wide ranges of climate, salinity, and sediment types. At all sites, biota (plankton, sediment living organisms, and fish) showed enhanced concentrations of Hg relative to corresponding organisms at nearby reference sites. The key process determining the risk at these sites is the net transformation of inorganic Hg to the highly toxic and bioavailable methylmercury (MeHg). Accordingly, Hg concentrations in Perca fluviatilis were more strongly correlated to MeHg (p < 0.05) than to inorganic Hg concentrations in the sediments. At all sites, except one, concentrations of inorganic Hg (2-55 microg g(-1)) in sediments were significantly, positively correlated to the concentration of MeHg (4-90 ng g(-1)). The MeHg/Hg ratio (which is assumed to reflect the net production of MeHg normalized to the Hg concentration) varied widely among sites. The highest MeHg/Hg ratios were encountered in loose-fiber sediments situated in southern freshwaters, and the lowest ratios were found in brackish-water sediments and firm, minerogenic sediments at the northernmost freshwater site. This pattern may be explained by an increased MeHg production by methylating bacteria with increasing temperature, availability of energy-rich organic matter (which is correlated with primary production), and availability of neutral Hg sulfides in the sediment pore waters. These factors therefore need to be considered when the risk associated with Hg-contaminated sediments is assessed. 相似文献
57.
Sjöström AE Collins CD Smith SR Shaw G 《Environmental pollution (Barking, Essex : 1987)》2008,156(3):1284-1289
Nonylphenol polyethoxylates (NPEOs) are surfactants found ubiquitously in the environment due to widespread industrial and domestic use. Biodegradation of NPEOs produces nonylphenol (NP), an endocrine disruptor. Sewage sludge application introduces NPEOs and NP into soils, potentially leading to accumulation in soils and crops. We examined degradation of NP and nonylphenol-12-ethoxylate (NP12EO) in four soils. NP12EO degraded rapidly (initial half time 0.3-5 days). Concentrations became undetectable within 70-90 days, with a small increase in NP concentrations after 30 days. NP initially degraded quickly (mean half time 11.5 days), but in three soils a recalcitrant fraction of 26-35% remained: the non-degrading fraction may consist of branched isomers, resistant to biodegradation. Uptake of NP by bean plants was also examined. Mean bioconcentration factors for shoots and seeds were 0.71 and 0.58, respectively. Removal of NP from the soil by plant uptake was negligible (0.01-0.02% of initial NP). Root concentrations were substantially higher than shoot and seed concentrations. 相似文献
58.
59.
Abrahamson A Brandt I Brunström B Sundt RC Jørgensen EH 《Environmental pollution (Barking, Essex : 1987)》2008,153(1):169-175
An ex vivo gill EROD assay was applied in Atlantic cod (Gadus morhua) as a biomarker for waterborne CYP1A-inducing compounds derived from oil production at sea. Exposure to nominal concentrations of 1 ppm or 10 ppm North Sea crude oil in a static water system for 24 h caused a concentration-dependent gill EROD induction. Further, exposure of cod for 14 days to environmentally relevant concentrations of produced water (PW, diluted 1:200 or 1:1000) from a platform in the North Sea using a flow-through system resulted in a concentration-dependent induction of gill EROD. Crude oil (0.2 ppm) from the same oil field also proved to induce EROD. Finally, gill EROD activity in cod caged for 6 weeks at 500-10 000 m from two platforms outside Norway was measured. The activities in these fish were very low and did not differ from those in fish caged at reference sites. 相似文献
60.
Levels of perfluorochemicals in water samples from Catalonia,Spain: is drinking water a significant contribution to human exposure? 总被引:2,自引:0,他引:2
Ericson I Nadal M van Bavel B Lindström G Domingo JL 《Environmental science and pollution research international》2008,15(7):614-619
Background, aim, and scope In recent years, due to a high persistence, biomagnification in food webs, presence in remote regions, and potential toxicity,
perfluorochemicals (PFCs) have generated a considerable interest. The present study was aimed to determine the levels of perfluorooctane
sulfonate (PFOS), perfluorooctanoic acid (PFOA), and other PFCs in drinking water (tap and bottled) and river water samples
from Tarragona Province (Catalonia, Spain).
Materials and methods Municipal drinking (tap) water samples were collected from the four most populated towns in the Tarragona Province, whereas
samples of bottled waters were purchased from supermarkets. River water samples were collected from the Ebro (two samples),
Cortiella, and Francolí Rivers. After pretreatment, PFC analyses were performed by HPLC-MS. Quantification was done using
the internal standard method, with recoveries between 68% and 118%.
Results In tap water, PFOS and PFOA levels ranged between 0.39 and 0.87 ng/L (0.78 and 1.74 pmol/L) and between 0.32 and 6.28 ng/L
(0.77 and 15.2 pmol/L), respectively. PFHpA, PFHxS, and PFNA were also other detected PFCs. PFC levels were notably lower
in bottled water, where PFOS could not be detected in any sample. Moreover, PFHpA, PFHxS, PFOA, PFNA, PFOS, PFOSA, and PFDA
could be detected in the river water samples. PFOS and PFOA concentrations were between <0.24 and 5.88 ng/L (<0.48 and 11.8 pmol/L)
and between <0.22 and 24.9 ng/L (<0.53 and 60.1 pmol/L), respectively.
Discussion Assuming a human water consumption of 2 L per day, the daily intake of PFOS and PFOA by the population of the area under evaluation
was calculated (0.78–1.74 and 12.6 ng, respectively). It was found that drinking water might be a source of exposure to PFCs
as important as the dietary intake of these pollutants.
Conclusions The contribution of drinking water (tap and bottled) to the human daily intake of various PFCs has been compared for the first
time with data from dietary intake of these PFCs. It was noted that in certain cases, drinking water can be a source of exposure
to PFCs as important as the dietary intake of these pollutants although the current concentrations were similar or lower than
those reported in the literature for surface water samples from a number of regions and countries.
Recommendations and perspectives Further studies should be carried out in order to increase the knowledge of the role of drinking water in human exposure to
PFCs. 相似文献