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181.
The Great Western Development Strategy (GWDS) is a long term national campaign aimed at boosting development of the western
area of China and narrowing the economic gap between the western and the eastern parts of China. The Strategic Environmental
Assessment (SEA) procedure was employed to assess the environmental challenges brought about by the western development plans.
These plans include five key developmental domains (KDDs): water resource exploitation and use, land utilization, energy generation,
tourism development, and ecological restoration and conservation. A combination of methods involving matrix assessment, incorporation
of expert judgment and trend analysis was employed to analyze and predict the environmental impacts upon eight selected environmental
indicators: water resource availability, soil erosion, soil salinization, forest destruction, land desertification, biological
diversity, water quality and air quality. Based on the overall results of the assessment, countermeasures for environmental
challenges that emerged were raised as key recommendations to ensure ecological security during the implementation of the
GWDS. This paper is intended to introduce a consensus-based process for evaluating the complex, long term pressures on the
ecological security of large areas, such as western China, that focuses on the use of combined methods applied at the strategic
level. 相似文献
182.
183.
184.
秦皇岛海岸侵蚀动态研究 总被引:2,自引:0,他引:2
刘松涛 《中国环境管理干部学院学报》2012,(1):25-28
利用不同时期的地形图、遥感图片对比,并选取典型海岸岸滩监测剖面实测数据,对海岸侵蚀现状进行了分析和定量计算。分析结果显示,秦皇岛海岸全线处于侵蚀状态,平均蚀退率1.5~4 m/a,根据蚀退率可将秦皇岛海岸划分为严重侵蚀、强侵蚀、侵蚀、微侵蚀、稳定5种岸线侵蚀类型。 相似文献
185.
A competitive indirect enzyme-linked immunoassay for lead ion measurement using mAbs against the lead-DTPA complex 总被引:1,自引:0,他引:1
Jun-jian Xiang Hong Wang Bin Liu Chang-wei Guo 《Environmental pollution (Barking, Essex : 1987)》2010,158(5):1376-314
Immunoassays for quantitative measurement of environmental heavy metals offer several advantages over other traditional methods. To develop an immunoassay for lead, Balb/c mice were immunized with a lead-chelate-protein conjugate to allow maximum exposure of the metal to the immune system. Three stable hybridoma cell lines were obtained through spleen cells fusion with Sp2/0 cells. One cell line, 2A11D11, produced mAbs with preferential selectivity and sensitivity for Pb-DTPA than DTPA, exhibiting an affinity constant of 3.34 ± 0.24 × 109 M−1. Cross reactivity (CR) with other metals were below 1%, except for Fe(III) with a CR less than 5%. This quantitative indirect ELISA for the lead ion was used to detect environmental lead content in local water sources; importantly, the results from the immunoassay were in excellent agreement with those from ICP-MS. Development of immunoassays for metal ions may thus facilitate the detection and regulation of environmental pollution. 相似文献
186.
Renbin Zhu Yashu Liu Hua Xu Tao Huang Jianjun Sun Erdeng Ma Liguang Sun 《Atmospheric environment (Oxford, England : 1994)》2010,44(3):304-311
During the summertime of 2007/2008, carbon dioxide (CO2) and methane (CH4) fluxes across air–water interface were investigated in the littoral zones of Lake Mochou and Lake Tuanjie, east Antarctica, using a static chamber technique. The mean fluxes of CO2 and CH4 were ?70.8 mgCO2 m?2 h?1 and 144.6 μgCH4 m?2 h?1, respectively, in the littoral zone of Lake Mochou; The mean fluxes were ?36.9 mgCO2 m?2 h?1 and 109.8 μgCH4 m?2 h?1, respectively, in the littoral zone of Lake Tuanjie. Their fluxes showed large temporal and spatial dynamics. The CO2 fluxes showed a significantly negative correlation with daily total radiation (DTR) and a weakly negative correlation with air temperature and water temperature, indicating that sunlight intensity controlled the magnitude of CO2 fluxes from the open lakes. The CH4 fluxes significantly correlated with local air temperature, water table and total dissolved solids (TDS), indicating that they were the predominant factors influencing CH4 fluxes. Summertime CO2 budgets in the littoral zones of Lake Mochou and Lake Tuanjie were estimated to be ?152.9 gCO2 m?2 and ?79.7 gCO2 m?2, respectively, and net CH4 emissions were estimated to be 312.3 mgCH4 m?2 and 237.2 mgCH4 m?2, respectively. Our results show that shallow, open, alga-rich lakes might be strong summertime CO2 absorbers and small CH4 emitters during the open water in coastal Antarctica. 相似文献
187.
David Widory Xiande Liu Shuping Dong 《Atmospheric environment (Oxford, England : 1994)》2010,44(30):3679-3687
Even after its being phased out in gasoline in the late 90s, lead (Pb) is still present at relatively high levels in the atmosphere of Beijing, China (0.10–0.18 μg m?3). Its origin is subject to debate as several distinct sources may contribute to the observed pollution levels. This study proposes to constrain the origin(s) of Pb and strontium (Sr) in aerosols, by coupling both Pb and Sr isotope systematics. The characterisation of the main pollution sources (road traffic, smelters, metal refining plants, coal combustion, cement factories, and soil erosion) shows that they can unambiguously be discriminated by the multi-isotope approach (206Pb/204Pb and 87Sr/86Sr). The study of total suspended particulates (TSP) and fine particles (PM2.5) from Beijing and its vicinity indicates that both size fractions are controlled by the same sources. Lead isotopes indicate that metal refining plants are the major source of atmospheric lead, followed by thermal power stations and other coal combustion processes. The role of this latter source is confirmed by the study of strontium isotopes. Occasionally, emissions from cement plants and/or input from soil alteration are isotopically detectable. 相似文献
188.
Jinzhu Ma Yongchun Liu Hong He 《Atmospheric environment (Oxford, England : 1994)》2010,44(35):4446-4453
To further understand the role of substrates on the heterogeneous reactions of polycyclic aromatic hydrocarbons, the reactions of ozone with anthracene adsorbed on different mineral oxides (SiO2, α-Al2O3 and α-Fe2O3) and on Teflon disc were investigated in dark at 20 °C. No reaction between ozone and anthracene on Teflon disc was observed when the ozone concentration was ~1.18 × 1014 molecules cm?3. The reactions on mineral oxides exhibited pseudo-first-order kinetics for anthracene loss, and the pseudo-first-order rate constant (k1,obs) displayed a Langmuir–Hinshelwood dependence on the gas-phase ozone concentration. The adsorption equilibrium constants for ozone (KO3) on SiO2-1, SiO2-2, α-Al2O3 and α-Fe2O3 were (0.81 ± 0.26) × 10?15 cm3, (2.83 ± 1.17) × 10?15 cm3, (2.48 ± 0.77) × 10?15 cm3 and (1.66 ± 0.45) × 10?15 cm3, respectively; and the maximum pseudo-first-order rate constant (k1,max) on these oxides were (0.385 ± 0.058) s?1, (0.101 ± 0.0138) s?1, (0.0676 ± 0.0086) s?1 and (0.0457 ± 0.004) s?1, respectively. Anthraquinone was identified as the main surface product of anthracene reacted with ozone. Comparison with previous research and the results obtained in this study suggest that the reactivity of anthracene with ozone and the lifetimes of anthracene adsorbed on mineral dust in the atmosphere are determined by the nature of the substrate. 相似文献
189.
颗粒物对无电压作用下离子交换膜分离去除铜离子的影响 总被引:1,自引:1,他引:0
在无外加电压条件下研究了颗粒物对阳离子交换膜分离去除铜离子效果的影响。选用硅酸、二氧化硅、氧化铝和水杨酸等4种物质作为颗粒物分别进行实验,其添加量均为50 mg/L。Cu2+及其补偿离子K+的浓度分别为0.0787mmol/L(5 mg/L)和0.787 mmol/L,水温为25±1℃,搅拌强度为600 r/min,水力停留时间为12 h。在所述实验条件下运行96 h后,水中无颗粒物干扰时,铜离子去除率为84%;水中存在带负电荷颗粒物(硅酸)和不带电荷颗粒物(二氧化硅和氧化铝)时,铜离子去除率略为下降至81%;而当水中存在带正电荷颗粒物(水杨酸)时,铜离子的去除率进一步下降为79%。研究结果表明带正电荷颗粒物对铜离子的交换去除影响较带负电荷或不带电荷颗粒物大,因为带正电荷颗粒物更易迁移至阳离子交换膜表面甚至进入膜内,并与膜表或膜内离子交换基团结合,从而导致铜离子交换去除明显下降。 相似文献
190.