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排序方式: 共有274条查询结果,搜索用时 15 毫秒
1.
研究了36个取代苯胺和苯酚类化合物对大型的急性毒性,应用正辛醇/水分配系数、线性溶解能关系参数和分子连接性指数得出了该类化合物的定量构效关系方程,这些方程可以用来进行该类化合物危害性初评.LSER法得到的QSAR方程拟合效果较好,增大分子体积及偶极性极化性,均可增大毒性.化合物与蛋白质等生物大分子的氢键键合作用是导致该类化合物毒性高于其基本毒性的原因.  相似文献   
2.
大地震在主破裂前往往行成地壳变形,高应力作用下进入峰值后的变形阶段,反映到地倾斜观测日均值曲线上,表现为固体潮形变趋势异常,这些异常能否指示远距离的地震,近年来不少研究者发现,远场前兆往往出现在对应力、应变变化反应灵敏的特殊构造部位。佳木斯台可能处于这种特殊的构造部位,对东北地区浅源地震短期前兆异常“场兆”的趋势性变化具有一定的意义。  相似文献   
3.

Polycyclic aromatic hydrocarbon (PAH) exposure and genetic susceptibility were conductive to genotoxic effects including gene damage, which can increase mutational probability. We aimed to explore the dose-effect associations of PAH exposure with damage of exons of epidermal growth factor receptor (EGFR) and breast cancer susceptibility gene 1 (BRCA1), as well as their associations whether modified by Flap endonuclease 1 (FEN1) genotype. Two hundred eighty-eight coke oven male workers were recruited, and we detected the concentration of 1-hydroxypyrene (1-OH-pyr) as PAH exposure biomarker in urine and examined base modification in exons of EGFR and BRCA1 respectively, and genotyped FEN1 rs174538 polymorphism in plasma. We found that the damage indexes of exon 19 and 21 of EGFR (EGFR-19 and EGFR-21) were both significantly associated with increased urinary 1-OH-pyr (both Ptrend < 0.001). The levels of urinary 1-OH-pyr were both significantly associated with increased EGFR-19 and EGFR-21 in both smokers and nonsmokers (both P < 0.001). Additionally, we observed that the urinary 1-OH-pyr concentrations were linearly associated with both EGFR-19 and EGFR-21 only in rs174538 GA+AA genotype carriers (both P < 0.001). Moreover, FEN1rs rs174538 showed modifying effects on the associations of urinary 1-OH-pyr with EGFR-19 and EGFR-21 (both Pinteraction < 0.05). Our findings revealed the linear dose-effect association between exon damage of EGFR and PAH exposure and highlight differences in genetic contributions to exon damage and have the potential to identify at-risk subpopulations who are susceptible to adverse health effects induced by PAH exposure.

  相似文献   
4.
根据环境保护部新发布的《关于执行大气污染物特别排放限值的公告》和GB13223-2011,结合重点地区石化企业燃煤发电锅炉的大气污染物排放情况,从脱硫、脱硝、除尘、脱汞4个方面对特别排放限值实施后可能对企业环保达标产生的影响进行了分析,并提出对策建议。  相似文献   
5.
The nitrogen (N) biological cycle of the Suaeda salsa marsh ecosystem in the Yellow River estuary was studied during 2008 to 2009. Results showed that soil N had significant seasonal fluctuations and vertical distribution. The N/P ratio (15.73±1.77) of S. salsa was less than 16, indicating that plant growth was limited by both N and P. The N absorption coefficient of S. salsa was very low (0.007), while the N utilization and cycle coefficients were high (0.824 and 0.331, respectively). The N turnover among compartments of S. salsa marsh showed that N uptake from aboveground parts and roots were 2.539 and 0.622 g/m2, respectively. The N translocation from aboveground parts to roots and from roots to soil were 2.042 and 0.076 g/m2, respectively. The N translocation from aboveground living bodies to litter was 0.497 g/m2, the annual N return from litter to soil was far less than 0.368 g/m2, and the net N mineralization in topsoil during the growing season was 0.033 g/m2. N was an important limiting factor in S. salsa marsh, and the ecosystem was classified as unstable and vulnerable. S. salsa was seemingly well adapted to the low-nutrient status and vulnerable habitat, and the nutrient enrichment due to N import from the Yellow River estuary would be a potential threat to the S. salsa marsh. Excessive nutrient loading might favor invasive species and induce severe long-term degradation of the ecosystem if human intervention measures were not taken. The N quantitative relationships determined in our study might provide a scientific basis for the establishment of effective measures.  相似文献   
6.
南昌市移动源排放清单研究   总被引:8,自引:4,他引:4  
根据收集的南昌市移动源活动水平数据,采用合适的估算方法、排放因子和GIS技术,建立了南昌市2007—2014年移动源排放清单,并对2014年移动源清单进行了空间化处理与分析,空间分辨率为1 km×1 km.结果表明,2007—2014年南昌市移动源共向大气排放CO、HC、NO_x、PM_(2.5)、PM_(10)、SO_2分别为18.26×10~4、5.07×10~4、18.46×10~4、0.99×10~4、1.08×10~4、3.31×10~4t.其中,2014年移动源向大气中排放的这6种污染物总量分别为2.14×10~4、0.76×10~4、1.97×10~4、0.08×10~4、0.09×10~4、0.55×10~4t.道路移动源中,汽油小型客车是CO、HC和SO_2最大的贡献源,排放量分别占机动车排放总量的55.1%、78.5%和56.1%;柴油重型货车是NO_x、PM_(2.5)和PM_(10)排放贡献率最大的车型,分别占43.2%、40%和40%.非道路移动源中,小型拖拉机对CO、HC、NO_x、PM_(2.5)和PM_(10)的贡献率均较大,分别占非道路移动源排放总量的29.9%、26.9%、23.4%、29.5%和29.8%;SO_2排放主要来源于船舶,占非道路移动源SO_2排放总量的45.1%.高污染排放集中的区域,主要是青山湖区、西湖区和东湖区.  相似文献   
7.
Concentrations of 15 polycyclic aromatic hydrocarbons (PAHs) were measured in surface soils collected from Dalian, China, for examination of distributions and composition profiles and their potential toxicity. The sum of 15 PAHs (SigmaPAHs) ranged from 190 to 8595 ng g(-1) dry weight, and showed an apparent urban-suburban-rural gradient in both SigmaPAHs and composition profiles. Using hierarchical cluster analysis (HCA), the sampling sites were grouped into four clusters corresponding to traffic area, park/residential area, suburban and rural areas. The ratios of naphthalene (Nap) and fluorene (Fl) versus fluoranthene (Flu), pyrene (Pyr) and indeno(1,2,3-cd)pyrene (InP) in the four clusters provided evidence of local distillation. The diagnostic ratios indicated the prevalent PAH sources were petroleum combustion and coal combustion in Dalian, and a cross plot of diagnostic ratios distinguished the urban samples from suburban and rural ones. Toxic potency assessment of soil PAHs presented a good relationship with benzo(a)pyrene (BaP) levels, toxic equivalent concentrations based on BaP (TEQ(BaP)) and dioxin-like toxic equivalent concentrations (TEQ(TCDD)). The study highlights that BaP is a good indicator for assessing the potential toxicity of PAHs, and presents a promising toxicity assessment method for soil PAHs.  相似文献   
8.
From April 2008 to November 2009, a field decomposition experiment was conducted to investigate the effects of sediment burial on macro (C, N) and microelement (Pb, Cr, Cu, Zn, Ni, and Mn) variations in decomposing litter of Phragmites australis in the coastal marsh of the Yellow River estuary. Three one-off sediment burial treatments [no sediment burial (0 mm year?1, S0), current sediment burial (100 mm year?1, S10), and strong sediment burial (200 mm year?1, S20)] were laid in different decomposition sites. Results showed that sediment burials showed significant influence on the decomposition rate of P. australis, in the order of S10 (0.001990 day?1)?≈?S20 (0.001710 day?1)?>?S0 (0.000768 day?1) (p?<?0.05). The macro and microelement in decomposing litters of the three burial depths exhibited different temporal variations except for Cu, Zn, and Ni. No significant differences in C, N, Pb, Cr, Zn, and Mn concentrations were observed among the three burial treatments except for Cu and Ni (p?>?0.05). With increasing burial depth, N, Cr, Cu, Ni, and Mn concentrations generally increased, while C, Pb, and Zn concentrations varied insignificantly. Sediment burial was favorable for C and N release from P. australis, and, with increasing burial depth, the C release from litter significantly increased, and the N in litter shifted from accumulation to release. With a few exceptions, Pb, Cr, Zn, and Mn stocks in P. australis in the three treatments evidenced the export of metals from litter to environment, and, with increasing burial depth, the export amounts increased greatly. Stocks of Cu and Ni in P. australis in the S10 and S20 treatments were generally positive, evidencing incorporation of the two metals in most sampling times. Except for Ni, the variations of C, N, Pb, Cr, Cu, Zn, and Mn stocks in P. australis in the S10 and S20 treatments were approximated, indicating that the strong burial episodes (S20) occurred in P. australis marsh in the future would have little influence on the stocks of these elements. With increasing burial depths, the P. australis was particularly efficient in binding Cu and Ni and releasing C, N, Pb, Cr, Zn, and Mn, implying that the potential eco-toxic risk of Pb, Cr, Zn, and Mn exposure might be very serious. This study emphasized the effects of different burials on nutrient and metal cycling and mass balance in the P. australis marsh of the Yellow River estuary.  相似文献   
9.
一直以来植物都是多领域的研究重点,随着非传统稳定同位素的不断发展,植物非传统稳定同位素研究日益增加。但因植物样品中有机物含量高,同位素分馏复杂,样品前处理及测定中存在诸多难题。本文对植物样品非传统稳定同位素工作中常用的前处理方法和测定技术进行了总结。综述了直接萃取法、湿法消解和高温灰化法的原理、操作和优缺点;以K、Ca、Mg、Fe、B等典型非传统稳定同位素为例介绍了非传统稳定同位素常用测定技术,旨在为植物样品的非传统稳定同位素测定进行梳理,最后对其应用方向和测试方法的发展方向进行了展望。  相似文献   
10.
• Selective molecularly imprinted polymer (MIP) binding gel was prepared. • MIP-DGT showed excellent uptake performance for antibiotics. • In situ measurement of antibiotics in wastewaters via MIP-DGT was developed. • The MIP-DGT method was robust, reliable, and highly sensitive. Urban wastewater is one of main sources for the introduction of antibiotics into the environment. Monitoring the concentrations of antibiotics in wastewater is necessary for estimating the amount of antibiotics discharged into the environment through urban wastewater treatment systems. In this study, we report a novel diffusive gradient in thin films (DGT) method based on molecularly imprinted polymers (MIPs) for in situ measurement of two typical antibiotics, fluoroquinolones (FQs) and sulfonamides (SAs) in urban wastewater. MIPs show specific adsorption toward their templates and their structural analogs, resulting in the selective uptake of the two target antibiotics during MIP-DGT deployment. The uptake performance of the MIP-DGTs was evaluated in the laboratory and was relatively independent of solution pH (4.0–9.0), ionic strength (1–750 mmol/L), and dissolved organic matter (DOM, 0–20 mg/L). MIP-DGT samplers were tested in the effluent of an urban wastewater treatment plant for field trials, where three SA (sulfamethoxazole, sulfapyridine, and trimethoprim) and one FQ (ofloxacin) antibiotics were detected, with concentrations ranging from 25.50 to 117.58 ng/L, which are consistent with the results measured by grab sampling. The total removal efficiency of the antibiotics was 80.1% by the treatment plant. This study demonstrates that MIP-DGT is an effective tool for in situ monitoring of trace antibiotics in complex urban wastewaters.  相似文献   
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