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321.
可吸入颗粒物生物活性及其微观特征分析 总被引:7,自引:3,他引:4
采用质粒DNA评价法研究了2004年春季北京市区和郊区上甸子(本底区)PM10的生物活性.结果表明,郊区上甸子2个PM10的TD20值(引起20%质粒DNA损伤所需要的颗粒物剂量)分别为53μg·mL-1和<50μg·mL-1,市区2个PM10的TD20值分别为125μg·mL-1和100μg·mL-1,说明郊区PM10的生物活性明显高于市区.同时利用高分辨率场发射扫描电镜(FESEM)和图像分析技术,从PM10微观特征上进行了生物活性差异的原因分析,认为其原因有:①上甸子PM10中以细颗粒物为主,在0~0.7μm粒度范围内的细颗粒物的数量百分含量明显高于市区PM10,而表面积则在0~1.0μm的范围内高于市区;②市区PM10中以粒度较大的矿物颗粒物为主,而上甸子PM10则以生物活性较大的烟尘为主,数量百分含量高达58.8%.因此PM10质量浓度并非评价可吸入颗粒物健康效应的唯一指标,颗粒物的粒度分布和类型可能在其生物活性中起重要作用. 相似文献
322.
Genotoxicity evaluation and a primary risk assessment of organic pollutants in the drinking water sources of Nanjing, China 总被引:2,自引:0,他引:2
An increasing number of industrial, agricultural, and commercial chemicals in the aquatic environment leads to various deleterious effects on organisms, which is becoming an increasingly serious problem in China. In this study, the comet assay was conducted to investigate the genotoxicity to human body caused by organic concentrates in the drinking water sources of Nanjing City from Yangtze River of China, and health and ecology risk due to expose to these organic pollutants were evaluated with the multimedia environmental assessment system (MEAS). For all the water samples, they were collected from four different locations in the drinking water sourcr samples, es of Nanjing City. The results of the comet assay showed that all the organic concentrates from the water samples could induce different levels DNA damages on human peripheral blood lymphocytes, and a statistically significant difference (p〈0.01) was observed compared with the solvent control, which demonstrated the genotoxicity was in existence. According to the ambient severity (AS) of individual compound, we had sorted out the main organic pollutants in the drinking water source of the four waterworks, and the results showed that there was some potential hazard to human body for all the source water, namely the total ambient severity (TAS) of health for each water source was more than 1. However, the TAS of ecology for each water source was less than 1, which indicated that it was safe to ecology. The results of this investigation demonstrate the application of the comet assay and the MEAS in aquatic environmental monitoring studies, and the comet assay found to be fast, sensitive, and suitable for genotoxicity monitoring programs of drinking water source. 相似文献
323.
Keiter S Rastall A Kosmehl T Wurm K Erdinger L Braunbeck T Hollert H 《Environmental science and pollution research international》2006,13(5):308-319
Goals, Scope and Background Fish populations, especially those of the grayling (Thymallus thymallus), have declined over the last two decades in the
upper Danube River between Sigmaringen and Ulm, despite intensive and continuous stocking and improvement of water quality
since the 1970s. Similar problems have been reported for other rivers, e.g. in Switzerland, Great Britain, the United States
and Canada. In order to assess if ecotoxicological effects might be related to the decline in fish catch at the upper Danube
River, sediment, suspended matter and waste water samples from sewage treatment plants were collected at selected locations
and analyzed in a bioanalytical approach using a battery of bioassays. The results of this pilot study will be used to decide
if a comprehensive weight-of-evidence study is needed.
Methods Freeze-dried sediments and suspended particulate matters were extracted with acetone in a Soxhlet apparatus. Organic pollutants
from sewage water were concentrated using XAD-resins. In order to investigate the ecotoxicological burden, the following bioassays
were used: (1) neutral red assay with RTL-W1 cells (cytotoxicity), (2) comet assay with RTLW1 cells (genotoxicity), (3) Arthrobacter
globiformis dehydrogenase assay (toxicity to bacteria), (4) yeast estrogen screen assay (endocrine disruption), (5) fish egg
assay with the zebrafish (Danio rerio; embryo toxicity) and (6) Ames test with TA98 (mutagenicity).
Results and Discussion The results of the in vitro tests elucidated a considerable genotoxic, cytotoxic, mutagenic, bacteriotoxic, embryotoxic and
estrogenic burden in the upper Danube River, although with a very inhomogeneous distribution of effects. The samples taken
from Riedlingen, for example, induced low embryo toxicity, but the second highest 17β-estradiol equivalent concentration (1.8
ng/L). Using the fish egg assay with native sediments, a broad range of embryotoxic effects could be elucidated, with clear-cut
dose-response relationships for the embryotoxic effects of contaminated sediments. With native sediments, embryotoxicity was
clearly higher than with corresponding pore waters, thus corroborating the view that – at least for fish eggs – the bioavailability
of particle-bound lipophilic substances in native sediments is higher than generally assumed. The effect observed most frequently
in the fish egg assay was a developmental delay. A comparison of our own results with locations along the rivers Rhine and
Neckar demonstrated similar or even higher ranges of ecotoxicological burdens in the Danube River.
Conclusions The complex pattern of ecotoxicological effects caused by environmental samples from the Danube River, when assessed in an
in vitro biotest battery using both acute and more specific endpoints, showed that integration of different endpoints is essential
for appropriate hazard assessment. Overall, the ecotoxicological hazard potential shown has indeed to be considered as one
potential reason for the decline in fish catches at the upper Danube River. However, based on the results of this pilot study,
it is not possible to elucidate that chemically induced alterations are responsible for the fish decline.
Recommendations and Perspective . In order to confirm the ecological relevance of the in vitro results for the situation in the field and especially for the
decline of the grayling and other fishes, further integrated investigations are required. For linking the weight of evidence
obtained by in vitro assays and fish population investigations, the application of additional, more specific biomarkers (e.g.
vitellogenin induction, EROD and micronucleus assay) has been initiated in fish taken from the field as well as in situ investigations. 相似文献
324.
以双特异分子探针技术(NPA-SH)为基础,运用电致化学发光技术(ECL)和磁性微球分选技术对其进行改进,成功建立了用于赤潮藻类定性定量分析的电致化学发光分子探针(ECL-MP)检测新技术.设计微小原甲藻特异性NPA探针并对其进行联吡啶钌和生物素标记,优化磁性微球使用量,在ECL检测装置中启动电化学反应,建立光信号与微小原甲藻细胞数目间的ECL-MP分析曲线并对其进行验证.结果表明,标记后的NPA探针具有一定的特异性和实用性;4μg是检测20μL目标藻杂交混合液的最适磁性微球使用量;在最适条件下,微小原甲藻细胞数的线性分析范围6.25×102~4×104个;比较ECL-MP和显微计数方法的样品检测结果,在95%置信区间内二者无显著差异(t-检验).ECL-MP方法为实现微小原甲藻现场样品的快速准确检测提供了一种新方法. 相似文献
325.
人体颊黏膜细胞彗星实验方法学研究 总被引:8,自引:0,他引:8
为探索一种简便、直接检测环境诱变物对人体靶细胞遗传毒性的方法,笔者以甲醛作为染毒剂,对人体口腔颊黏膜细胞彗星实验的染毒时间、染毒温度和2种用于检测交联作用的方案进行了研究。结果显示:经7 5μmol L甲醛37℃染毒30和60min后,DNA的断裂程度较染毒15min更大;而经该浓度甲醛在4,23和37℃下染毒30min后均可引起DNA的断裂,但37℃下染毒对DNA的断裂作用更大。在2种应用于检测交联作用的方案中,加大电泳条件的交联检测方案还可检测兼具交联和断裂效应的诱变物。 相似文献
326.
327.
纳米MnO2与常规MnO2粉末对Hela细胞DNA损伤的对比研究 总被引:3,自引:8,他引:3
为探讨纳米MnO2与常规MnO2粉末对细胞DNA损伤作用的差别,采用不同浓度的纳米MnO2与常规MnO2粉末(0、100、200、400μg·mL-1)对Hela细胞进行染毒,应用单细胞凝胶电泳(彗星实验)检测Hela细胞的损伤效应.结果表明,与对照组相比,纳米MnO2和常规MnO2各染毒组细胞尾部DNA百分率(TailDNA%)和尾矩(TailMoment)均显著增加(p<0.01);同一浓度下,纳米MnO2组细胞尾部DNA百分率和尾矩显著高于常规MnO2组(p<0.01).以上结果表明,纳米MnO2和常规MnO2粉末均能导致Hela细胞DNA损伤,且纳米MnO2的损伤作用强于常规MnO2. 相似文献