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1.
Abstract: Broadly conceived and considered in its many usages, sustainability has grave defects as a planning goal, particularly when used by conservationists: it confuses means and ends; it is vague about what is being sustained and who or what is doing the sustaining; it is uninspiring; it is little more than Pinchot-era conservation (and thus ignores the many lessons learned since then); it need not be linked to land, to the land's functioning, or to any ecological science; it need not include a moral component; it is consistent with the view of humans as all-powerful manipulators of the planet; and, in general, it is such a malleable term that its popularity provides only a facade of consensus. When sustainability is defined broadly to include the full range of economic and social aspirations, it poses the particular risk that ecological and biodiversity concerns will be cast aside in favor of more pressing human wants. Given these many defects, the conservation movement should discard the term in favor of a more alluring goal, attentive to nature and its ecological functioning. A sound goal would incorporate and distill the considerable ecological and moral wisdom accumulated since Pinchot's day while giving conservationists the rhetorical tools needed to defend the land against competing pressures. In our view, conservation would be well served by an updated variant of "land health," Aldo Leopold's ecologically grounded goal from the 1940s. Land health as an independent understanding should set the essential terms of how we live and enjoy the earth, providing the framework within which we pursue our many social and economic aims. 相似文献
2.
Marzena Matejczyk Piotr Ofman Katarzyna Dąbrowsk Renata Świsłock Włodzimierz Lewandowski 《环境科学学报(英文版)》2020,32(5):128-141
In the present work we compared the biological activity of DCF, 4′-OHDCF and 5-OHDCF as molecules of most biodegradation pathways of DCF and selected transformation products (2-hydroxyphenylacetic acid; 2,5-dihydroxyphenylacetic acid and 2,6-dichloroaniline) which are produced during AOPs, such as ozonation and UV/H2O2. We also examined the interaction of DCF with chlorogenic acid (CGA). CGA is commonly used in human diet and entering the environment along with waste mainly from the processing and brewing of coffee and it can be toxic for microorganisms included in activated sludge. In the present experiment the evaluation of following parameters was performed: E. coli K-12 cells viability, growth inhibition of E. coli K-12 culture, LC50 and mortality of Chironomus aprilinus, genotoxicity, sodA promoter induction and ROS generation. In addition the reactivity of E. coli SM recA:luxCDABE biosensor strain in wastewater matrices was measured. The results showed the influence of DCF, 4′-OHDCF and 5-OHDCF on E. coli K-12 cells viability and bacteria growth, comparable to AOPs by-products. The highest toxicity was observed for selected, tested AOPs by-products, in comparison to the DCF, 4′-OHDCF and 5-OHDCF. Genotoxicity assay indicated that 2,6-dichloroaniline (AOPs by-product) had the highest toxic effect. The oxidative stress assays revealed that the highest level of ROS generation and sodA promoter induction were obtained for DCF, 4′-OHDCF and 5-OHDCF, compared to other tested compounds. We have also found that there is an interaction between chlorogenic acid and DCF, which resulted in increased toxicity of the mixture of the both compounds to E. coli K-12, comparable to parent chemicals. The strongest response of E. coli SM biosensor strain with recA:luxCDABE genetic construct in filtered treated wastewaters, comparable to control sample was noticed. It indicates, that E. coli SM recA:luxCDABE biosensor strains is a good tool for bacteria monitoring in wastewater environment. Due to toxicity and biological activity of tested DCF transformation products, there is a need to use additional wastewater treatment systems for wastewater contaminated with pharmaceutical residues. 相似文献
3.
基于经过验证的三维水动力-水质模型,对珠江口夏季有机碳进行海陆源区分,并对海陆源有机碳的分布特征、贡献比重及其通量过程进行研究.结果表明,水平方向上,珠江口夏季陆源(海源)有机碳浓度从口门到外海逐渐降低(升高),在表、底层海水中平均浓度分别为1.45和0.87mg/L(0.97和1.05mg/L);垂直方向上,在层化水域陆源(海源)有机碳浓度从上到下逐渐递减(升高),在非层化水域海陆源有机碳浓度垂向分布较为均匀.珠江口夏季海源有机碳贡献率表层海水低于底层海水,平均贡献率为48.26%,沿向海方向海源有机碳贡献率逐渐增加--从内伶仃洋水域的4.43%逐渐提升到外伶仃洋东侧水域的81.20%.珠江口水动力条件复杂,在径流、潮汐、季风等因素的作用下陆源有机碳向海输送且向海输送量逐渐递减;海源有机碳在不同水域动力输送特征不同,西南水域向海输送,向海输送量逐渐递增;东北水域向岸输送,向岸输送量逐渐递减.陆源有机碳生化反应活性较弱,只有小部分被生化过程消耗,其迁移转化主要由沉降过程控制,而海源有机碳的迁移转化,则由口门的动力输送过程主控向外海的生化耗碳过程主控过渡.此外,海源有机碳沉降作用明显低于陆源有机碳,生化作用明显高于陆源有机碳. 相似文献
4.
Sulphate, Nitrogen and Base Cation Budgets at 21 Forested Catchments in Canada, the United States and Europe 总被引:1,自引:0,他引:1
Watmough SA Aherne J Alewell C Arp P Bailey S Clair T Dillon P Duchesne L Eimers C Fernandez I Foster N Larssen T Miller E Mitchell M Page S 《Environmental monitoring and assessment》2005,109(1-3):1-36
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
5.
微电解-水解酸化/接触氧化工艺处理染化废水的研究 总被引:18,自引:0,他引:18
采用微电 解 H/ O 工艺对染 料化 工 废水 进行 了 处理 研究 ,结 果表 明 以微 电解 和 水解 酸 化作预处理 ,可使废 水的 B O D5/ C O D Cr 的比由 025 提高 到05 0 左 右,平 均 增加 50 % 。通 过加 酸, 可提高微电 解的去除 效果,在 进水 C O D Cr 为4 100 ~4 300 m g/ L,色度 为3 400 ~3 600( 倍) 范围内 ,系统对 C O D Cr 和色度 的去除效 果分别 可达到97 5 % 和983 % 相似文献
6.
感光胶片废水的水解酸化—好氧处理工艺试验 总被引:1,自引:0,他引:1
对感光胶片有机生产废水处理工艺进行了方法采用水解酸化-好氧串联工艺和传统活性污泥法两种方法并进行对照。结果经水解酸化处理,废水的BOD5/CODcr可提高至0.54-0.56,平均增加了17%左右,证实了水解酸化菌在该工艺条件下具有搞高效片废水可生化性的功能。 相似文献
7.
8.
介绍了采用中和混凝 水解酸化 生物接触氧化 化学除磷工艺对可发性聚苯乙烯 (EPS)废水的处理工艺。在废水中的CODCr、TP、SS、NH3 N分别为 194 0mg L、112mg L、5 92mg L、2 3 6mg L的条件下 ,废水经过处理后 ,出水CODCr、TP、SS、NH3 N分别为 70mg L、0 38mg L、2 6mg L、0 32mg L ,均可达到《污水综合排放标准》中的一级标准 ,废水中CODCr、TP、SS、NH3 N的平均去除率分别为 96 4 %、99 3%、95 6 %、98 6 %。 相似文献
9.
10.
大照彬 《辽宁城乡环境科技》2007,27(3):52-54
文中讨论了水解酸化-好氧-生物炭及水解酸化-好氧-气浮工艺处理印染废水时的优缺点,采用上述工艺印染污水,可使CODcr:1000mg/L、BOD5:300mg/L、ss:300mg/L、色度:〉300倍的印染废水达标排放. 相似文献