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461.
精神活性物质是一类摄入人体后对中枢神经系统具有强烈兴奋或抑制作用的新型污染物,其在水环境中的存在可能对水生生物、水生态系统甚至人体健康产生潜在的危害。为评价太湖中精神活性物质的污染水平和生态风险,利用超高效液相色谱-质谱联用法检测了太湖19条入湖河流中13种典型精神活性物质的质量浓度和空间分布规律。结果表明,在太湖19条入湖河流中除苯甲酰牙子碱(BE)和去甲氯胺酮(NK)外,其余11种目标物均有检出,质量浓度范围为n.d.~43.2 ng·L~(-1)。其中麻黄碱(EPH)的检出率和中间浓度最高,分别为100%和11.0 ng·L~(-1);其次为甲基苯丙胺(METH),检出频率为58%,浓度中值为1.0 ng·L~(-1);苯丙胺(AMP)在东部湖区均未检出。大部分精神活性物质浓度水平较高的河流分布在竺山湾和西太湖,而海洛因(HR)的高值区主要在南太湖。运用风险熵方法对其进行风险评估,结果显示,太湖流域地表水中检出的13种精神活性物质的风险熵值均<0.1,生态风险较低,但其对水生生态系统的长期和综合风险值得关注。 相似文献
462.
以人工湿地修复镉污染水体时,植物在镉离子的沉淀、吸收和积累等过程中起着关键作用,但当前报道的镉富集植物种类较少,湿地植物对镉胁迫的生长及生理响应缺乏系统研究,限制了湿地植物在镉污染水体修复中的应用。笔者以常见湿地植物水蓼(Polygonum hydropiper L.)为对象,设置了4个镉处理浓度(0、0.5、1和2 mg·L~(-1)),研究了水蓼对镉的富集特征以及生长和生理响应。水蓼根、茎和叶的镉含量(以干重计)随镉处理浓度的增加而升高,处理30 d时,在2 mg·L~(-1)处理下分别达到134、47和48 mg·kg~(-1)。处理30 d时,在1 mg·L~(-1)的镉处理下,水蓼的地上部及地下部富集系数和转运系数最高,地上部和地下部富集系数分别为45.6和111.7,转运系数为0.41。在处理15 d时,水蓼生物量、叶绿素含量和超氧化物歧化酶(SOD)活性在2 mg·L~(-1)处理下显著降低。在处理30 d时,水蓼的总生物量在不同镉浓度下无显著差异,但丙二醛(MDA)含量、SOD和过氧化氢酶(CAT)活性在0.5~2 mg·L~(-1)镉处理下均显著升高,叶绿素含量下降。这些结果表明,水蓼可以通过提高抗氧化酶活性等机理抵抗镉胁迫产生的氧化伤害,并且水蓼对镉的富集和转运系数较高,具有在镉污染水体修复中应用的潜力。 相似文献
463.
Chao Lu Kanglan Deng Chun Hu Lai Lyu 《Frontiers of Environmental Science & Engineering》2020,14(5):82
464.
造纸污泥固化/稳定化处理技术研究 总被引:4,自引:2,他引:2
为了能更好地无害化处理造纸污泥,对造纸污泥的固化/稳定化处理技术进行了研究。以水泥、粉煤灰和煤渣作为固化剂对造纸污泥进行固化/稳定化处理。通过抗压强度评价污泥固化块的力学性质;并对固化块浸出液的COD浓度与重金属质量浓度进行了检测。当水泥、粉煤灰和煤渣的掺量分别为0.12、0.02和0.10 kg/kg,养护时间为6 d时,固化块抗压强度达到360 kPa。结果表明,水泥和煤渣对提高造纸污泥固化块的抗压强度具有促进作用,而它们与粉煤灰对造纸污泥中的有机质和重金属均具有一定的固化作用。在以上条件下,固化块浸出液中COD浓度约为115.7 mg/L,重金属浓度符合国家标准。经养护后的固化块含水率均保持在35%~40%,符合填埋场的进场标准。 相似文献
465.
大气气溶胶酸度的研究进展 总被引:1,自引:0,他引:1
大气气溶胶的环境效应、气候效应和健康效应均与气溶胶的物理化学性质直接相关,其中大气气溶胶酸度是其重要的性质之一。大气气溶胶酸度对酸沉降、灰霾的形成具有重要作用,并影响大气非均相化学反应,相关研究已成为国际研究的热点。对国内外学者近年来在大气气溶胶酸度对大气环境与人体健康的影响、大气气溶胶酸度的影响因素与变化规律、大气气溶胶酸度/酸化缓冲能力的测定与计算方法、大气气溶胶酸性成分采集系统等方面的研究进展作了较系统的综述,并对大气气溶胶酸度研究未来的发展进行了展望。 相似文献
466.
Quantifying Terrestrial Ecosystem Carbon Dynamics in the Jinsha Watershed, Upper Yangtze, China from 1975 to 2000 总被引:1,自引:0,他引:1
Shuqing Zhao Shuguang Liu Runsheng Yin Zhengpeng Li Yulin Deng Kun Tan Xiangzheng Deng David Rothstein Jiaguo Qi 《Environmental management》2010,45(3):466-475
Quantifying the spatial and temporal dynamics of carbon stocks in terrestrial ecosystems and carbon fluxes between the terrestrial
biosphere and the atmosphere is critical to our understanding of regional patterns of carbon budgets. Here we use the General
Ensemble biogeochemical Modeling System to simulate the terrestrial ecosystem carbon dynamics in the Jinsha watershed of China’s
upper Yangtze basin from 1975 to 2000, based on unique combinations of spatial and temporal dynamics of major driving forces,
such as climate, soil properties, nitrogen deposition, and land use and land cover changes. Our analysis demonstrates that
the Jinsha watershed ecosystems acted as a carbon sink during the period of 1975–2000, with an average rate of 0.36 Mg/ha/yr,
primarily resulting from regional climate variation and local land use and land cover change. Vegetation biomass accumulation
accounted for 90.6% of the sink, while soil organic carbon loss before 1992 led to a lower net gain of carbon in the watershed,
and after that soils became a small sink. Ecosystem carbon sink/source patterns showed a high degree of spatial heterogeneity.
Carbon sinks were associated with forest areas without disturbances, whereas carbon sources were primarily caused by stand-replacing
disturbances. It is critical to adequately represent the detailed fast-changing dynamics of land use activities in regional
biogeochemical models to determine the spatial and temporal evolution of regional carbon sink/source patterns. 相似文献
467.
Radiation with UV-B increased the damage to DNA in Scytonema javanicum, a desert-dwelling soil microorganism, and the level of damage varied with the intensity of UV-B radiation and duration of exposure. Production of reactive oxygen species (ROS) also increased because of the radiation. Different exogenous chemicals (ascorbate acid, ASC; N-acetylcysteine, NAC; glyphosate, GPS; and 2-methyl-4-chlorophenoxyacetic acid, MCPA-Na) differed in their effect on the extent of DNA damage and ROS production: whereas NAC and ASC protected the DNA from damage and resulted in reduced ROS production, the herbicides (GPS and MCPA-Na) increased the extent of damage, lowered the rate of photosynthesis, and differed in their effect on ROS production. The chemicals probably have different mechanisms to exercise their effects: NAC and ASC probably function as antioxidant agents or as precursors of other antioxidant molecules that protect the DNA and photosynthetic apparatus directly from the ROS produced as a result of UV-B radiation, and GPS and MCPA-Na probably disrupt the normal metabolism in S. javanicum to induce the leaking of ROS into the photosynthetic electron transfer pathway following UV-B radiation, and thereby damage the DNA. Such mechanisms have serious implications for the use of environment-friendly herbicides, which, because they can destroy DNA, may prove harmful to soil microorganisms. 相似文献
468.
采用水热法制备出LiFePO4催化剂,通过电子显微镜(SEM)、X射线衍射(XRD)和傅立叶红外光谱(FTIR)对其进行表征,并将其作为非均相Fenton催化剂处理亚甲基蓝(MB)染料溶液。实验结果表明,在催化剂用量为4 g/L,H2O2浓度为0.04 mol/L,pH值为3,温度为50℃,反应时间为60 min的条件下,浓度为500 mg/L的亚甲基蓝脱色率达99%。根据实验结果,讨论了LiFePO4作为非均相Fenton催化剂对亚甲基蓝的降解机理。 相似文献
469.
Deng Y Besse-Hoggan P Husson P Sancelme M Delort AM Stepnowski P Paszkiewicz M Gołębiowski M Costa Gomes MF 《Chemosphere》2012,89(3):327-333
Several physico-chemical properties relevant to determine the environmental impact of ionic liquids - aqueous solubility, octanol/water partition coefficient, chromatographically derived lipophilicity and infinite dilution diffusion coefficients in water - were measured in ionic liquids based on pyridinium, ammonium and pyrrolidinium cations with bis(trifluoromethylsulfonyl)imide anions. The influence of the presence of hydroxyl or ester groups in the physico-chemical properties of these liquids was checked. It appeared that the presence of functional oxygenated moieties reduces the lipophilicity of ionic liquids and so decreases the risk of bioaccumulation in environment. 相似文献
470.
Burial of terrestrial and marine organic carbon in Jiaozhou Bay: different responses to urbanization 总被引:3,自引:0,他引:3
Yang Liyang Wu Ying Zhang Jing Liu Sumei Deng Bing 《Regional Environmental Change》2011,11(3):707-714
Organic geochemical proxies (OC, OC/TN, δ13C, and lignin oxidation products) were measured in a 271 cm long sediment core collected from central Jiaozhou Bay, northern
China, to study the response of terrestrial and marine organic carbon burials to the surrounding urbanization. Terrestrial
organic carbon content was constantly low from the bottom of the core to ~150 cm depth, indicating a stable and low level
of terrestrial input before urbanization. Thereafter, it increased up to ~20 cm depth, suggesting that increased human activities
and land-use changes during urbanization likely enhanced the flux of terrestrial organic carbon to the bay. Overall, 5–38%
of the total organic carbon was terrigenous, which was derived from a mixture of woody and non-woody angiosperms and moderately
degraded. Marine organic carbon content did not increase notably during urbanization. It increased from the bottom of the
core to ~180 cm and stayed at high levels until it decreased in the top 20 cm. It was affected by multiple factors, including
grain size and nutrient composition. These results demonstrate the different influences of urbanization on terrestrial and
marine organic carbon cycles and suggest the importance of discriminating between these two organic carbon pools in the reconstruction
of their historical changes. 相似文献