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81.
Laura J. Sonter Megan Barnes Jeffrey W. Matthews Martine Maron 《Conservation Letters》2019,12(3):e12629
Compensation policies seek to counterbalance biodiversity losses caused by development; however, their effectiveness is rarely tested. We examined U.S. Species Conservation Banks (SCBs) in California, a compensation program initiated 30 years ago. We quantified the effect of 59 SCBs (15,350 ha) on habitat extent using statistical matching methods. SCBs averted a small, yet significant, amount of habitat loss (62 ha) between 2001 and 2011. However, unexpectedly, SCBs also averted significant habitat gains (1,424 ha). It is not possible to determine if losses averted by SCBs equaled losses caused by development for which credits were sold (because records of the latter do not exist), but estimated averted gains were 35 times greater than averted losses. To improve practice, SCBs must be designed to achieve outcomes that are additional and avoid crowding out other programs incentivizing statewide conservation goals. 相似文献
82.
Moshe Fejgin MD Inbal Barnes Noami Lipnick Zipporah Magid Gertrude Kohn Aliza Amiel 《黑龙江环境通报》1992,12(2):129-131
We report a case in which mosaicism of trisomy 13 was detected in 4/10 cells (40 per cent) in amniotic fluid cell cultures, followed by a low rate of mosaicism (1/160 cells) detected in a fetal blood sample. This finding presents a dilemma both for the genetic counsellor and for the parents in determining whether or not to terminate the pregnancy. 相似文献
83.
84.
Seasonal changes of respiratory metabolism and biochemical composition were studied in Actinia equina L. (Cnidaria: Anthozoa) collected in 1982 and 1983 from two shore locations in Spain. Changes of metabolic activity follow closely those of biochemical constituents, particularly carbohydrates and lipids, showing maxima in late fall and spring. Weight dependence, established according to the exponential equation y=a xb (x=weight), results in virtually isometric relationships for proteins, total lipids and sugars but not glycogen. Allometry for this last compound represents a reduction in glycogen level in connection with size decrease; this weight effect declines when glycogen levels rise, both in field and laboratory fed anemones, thus suggesting a stronger influence of food availability on storage in small anemones. 相似文献
85.
Isotopic exchange occurs between coral skeleton and 45Ca++ and H14CO
3
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in seawater. Exchange of 14C onto skeletons is more rapid than exchange of 45Ca++. Exchange of 14C from skeletons to seawater takes place more slowly than exchange of 45Ca++ to seawater. When living coral is incubated in the dark with radioisotopes for 1 h, the tissues contain considerably more radioactivity than is associated with the skeleton. The tissue radioactivity reflects permeation of tissues and coelenteron by radioactive compounds from the incubation seawater. Addition of alkalis to cardioactive seawater results in a radioactive precipitate, part of which becomes associated with any coral skeleton present, and part of which forms on the wall of the containing vessel. Strong alkali removes biologically-deposited radioisotope from coral skeletons. Deposition, of 14C from H14CO
3
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in skeletons of living coral incubated in the dark is greater than in dead coral. The reverse situation occurs with 45Ca++. 相似文献
86.
James E. M. Watson Emily S. Darling Oscar Venter Martine Maron Joe Walston Hugh P. Possingham Nigel Dudley Marc Hockings Megan Barnes Thomas M. Brooks 《Conservation biology》2016,30(2):243-248
Recognizing that protected areas (PAs) are essential for effective biodiversity conservation action, the Convention on Biological Diversity established ambitious PA targets as part of the 2020 Strategic Plan for Biodiversity. Under the strategic goal to “improve the status of biodiversity by safeguarding ecosystems, species, and genetic diversity,” Target 11 aims to put 17% of terrestrial and 10% of marine regions under PA status by 2020. Additionally and crucially, these areas are required to be of particular importance for biodiversity and ecosystem services, effectively and equitably managed, ecologically representative, and well‐connected and to include “other effective area‐based conservation measures” (OECMs). Whereas the area‐based targets are explicit and measurable, the lack of guidance for what constitutes important and representative; effective; and OECMs is affecting how nations are implementing the target. There is a real risk that Target 11 may be achieved in terms of area while failing the overall strategic goal for which it is established because the areas are poorly located, inadequately managed, or based on unjustifiable inclusion of OECMs. We argue that the conservation science community can help establish ecologically sensible PA targets to help prioritize important biodiversity areas and achieve ecological representation; identify clear, comparable performance metrics of ecological effectiveness so progress toward these targets can be assessed; and identify metrics and report on the contribution OECMs make toward the target. By providing ecologically sensible targets and new performance metrics for measuring the effectiveness of both PAs and OECMs, the science community can actively ensure that the achievement of the required area in Target 11 is not simply an end in itself but generates genuine benefits for biodiversity. 相似文献
87.
Judith Schleicher Johanna Eklund Megan D. Barnes Jonas Geldmann Johan A. Oldekop Julia P. G. Jones 《Conservation biology》2020,34(3):538-549
The awareness of the need for robust impact evaluations in conservation is growing and statistical matching techniques are increasingly being used to assess the impacts of conservation interventions. Used appropriately matching approaches are powerful tools, but they also pose potential pitfalls. We outlined important considerations and best practice when using matching in conservation science. We identified 3 steps in a matching analysis. First, develop a clear theory of change to inform selection of treatment and controls and that accounts for real-world complexities and potential spillover effects. Second, select the appropriate covariates and matching approach. Third, assess the quality of the matching by carrying out a series of checks. The second and third steps can be repeated and should be finalized before outcomes are explored. Future conservation impact evaluations could be improved by increased planning of evaluations alongside the intervention, better integration of qualitative methods, considering spillover effects at larger spatial scales, and more publication of preanalysis plans. Implementing these improvements will require more serious engagement of conservation scientists, practitioners, and funders to mainstream robust impact evaluations into conservation. We hope this article will improve the quality of evaluations and help direct future research to continue to improve the approaches on offer. 相似文献
88.
Erin L. Murphy Miranda Bernard Gwenllian Iacona Stephanie B. Borrelle Megan Barnes Alexis McGivern Jorge Emmanuel Leah R. Gerber 《Conservation biology》2022,36(2):e13827
Marine plastic pollution has emerged as one of the most pressing environmental challenges of our time. Although there has been a surge in global investment for implementing interventions to mitigate plastic pollution, there has been little attention given to the cost of these interventions. We developed a decision support framework to identify the economic, social, and ecological costs and benefits of plastic pollution interventions for different sectors and stakeholders. We calculated net cost as a function of six cost and benefit categories with the following equation: cost of implementing an intervention (direct, indirect, and nonmonetary costs) minus recovered costs and benefits (monetary and nonmonetary) produced by the interventions. We applied our framework to two quantitative case studies (a solid waste management plan and a trash interceptor) and four comparative case studies, evaluating the costs of beach cleanups and waste-to-energy plants in various contexts, to identify factors that influence the costs of plastic pollution interventions. The socioeconomic context of implementation, the spatial scale of implementation, and the time scale of evaluation all influence costs and the distribution of costs across stakeholders. Our framework provides an approach to estimate and compare the costs of a range of interventions across sociopolitical and economic contexts. 相似文献
89.
Almost 2000 cheilostomatid–cheilostomatid (bryozoan) interactions were recorded from 110 rocks from intertidal and infralittoral
zone locations at Kodiac Island in the Alaskan Boreal–Arctic. Intraspecific interactions were unusually rare; this may have
resulted from inhibition of con-specific settlement by adult colonies. In one species, rank did vary as a function of depth.
The proportion of determinate-species encounter-pairings (a pairing in which one competitor/species wins all encounters) and
tied outcomes (whereby neither competitor/species wins or loses but are involved in a “standoff” or mutual overgrowth) increased
from the upper midlittoral to the lower infralittoral. The assemblage of bryozoans formed a clear hierarchy, with a score
of 0.83 on Tanaka and Nandakumar's transitivity index. Overgrowth dominants did not monopolise the assemblage. The most abundant
species were mid- or lower-ranked competitors. The identity of the competitive species had a major influence on the outcome
of encounters. Zooidal height and colony growth morphology were important factors determining overall overgrowth rank. The
greatest number of interaction types was recorded on medium-sized (surface area >300 and <600 cm2) rocks, and the overall diversity of intertidal species was very high compared with studies conducted elsewhere. The high
interaction and species diversity recorded may both have resulted from intermediate levels of disturbance.
Received: 16 July 1998 / Accepted: 14 December 1999 相似文献
90.
In order to study taxon richness, biodiversity and abundance patterns in the North Atlantic from temperate latitudes through Arctic to high Arctic latitudes, we recorded the faunas (at ELWS level) colonizing 20 cobbles from three sites at each of seven boulder-field localities (south-west England, 50°N; Wales, 51°N; west Scotland, 56°N; Iceland, 64°N; Tromsø, 70°N; Svalbard, 77°N, 79°N). Inverse correlations were found between latitude and all measures of richness (species, orders, and phyla numbers) and biodiversity (S–W, P). However, these correlations were driven mostly by the consistently impoverished Arctic sites; an even cline of decreasing diversity from south to north did not exist. Multidimensional scaling revealed two communities, temperate–subarctic species-rich and high arctic species-poor. Evenness as measured by Pielou’s index was similar across all latitudes. Abundance data exhibited a similar trend to the species richness and diversity data with a significant negative correlation with latitude, but when Arctic data were excluded the correlation vanished. 相似文献