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株洲市工业区大气中SO2转化速率的研究 总被引:2,自引:0,他引:2
在湖南省株洲市工业区的下风向布点,同时测定大气中SO2的浓度、TSP和<0.25μm细粒子中SO2-4的浓度.结果表明,大气中SO2浓度随着离污染源距离的增加迅速下降,和SO2相比,颗粒物中SO2-4浓度随距离的增加而降低的程度要慢得多.同步测定的SO2浓度和细粒子SO2-4浓度有显著的相关关系.根据风向、风速和新产生的细粒子中的SO2-4浓度及大气中SO2的浓度计算了株洲教育学院处SO2的转化速率,春季湿度大,SO2转化速率也大,为4.8%/h,秋季湿度小,SO2的转化速率变低,为1.5%/h.春季中路铺SO2转化速率为3.1%/h. 相似文献
175.
Gerald Spindler Konrad Müller Hartmut Herrmann 《Environmental science and pollution research international》1999,6(2):89-94
Aerosol filter samples have been collected nearby the industrialised basin of Leipzig in Saxony (Germany) at the research station Melpitz of the Institut für Troposphärenforschung e.V. (IfT). Time series (1992–1998) and a three year comparison (1995–1997) of two different aerosol filter sampling systems, the Sierra-Andersen-PM 10 high volume sampler (daily sample, PM 10 inlet) and the Rupprecht and Patashnik Co. Inc. Model Partisol 2000 (weekly sample, PM 10 and PM 2.5 inlet) are presented and discussed. The comparison of the different sampling systems and strategies yields small differences between the daily and weekly samples for mass and different ions, which may be influenced by sampling duration and flow rates. A general trend of change in aerosol composition was observed: Soot and Sulphate concentrations decreased whereas Nitrate and Ammonium concentrations increased. During summers the mass of coarse particles is higher than in other seasons. One reason could be found in the occurence of longer periods of dry ground surfaces enabling reemission of crustal and biological material. The time series have been integrated in a longer historical aerosol mass trend for Saxony and do show a good agreement. Since 1990 a significant downward trend in gravimetric mass concentration was found. 相似文献
176.
An overview of the application of organic geochemistry to the analysis of organic matter on aerosol particles is presented
here. This organic matter is analyzed as solvent extractable bitumen/ lipids by gas chromatography-mass spectrometry. The
organic geochemical approach assesses the origin, the environmental history and the nature of secondary products of organic
matter by using the data derived from specific molecular analyses. Evaluations of production and fluxes, with cross-correlations
can thus be made by the application of the same separation and analytical procedures to samples from point source emissions
and the ambient atmosphere. This will be illustrated here with typical examples from the ambient atmosphere (aerosol particles)
and from emissions of biomass burning (smoke).
Organic matter in aerosols is derived from two major sources and is admixed depending on the geographic relief of the air
shed. These sources are biogenic detritus (e.g., plant wax, microbes, etc.) and anthropogenic particle emissions (e.g., oils,
soot, synthetics, etc.). Both biogenic detritus and some of the anthropogenic particle emissions contain organic materials
which have unique and distinguishable compound distribution patterns (C14-C40). Microbial and vascular plant lipids are the dominant biogenic residues and petroleum hydrocarbons, with lesser amounts
of the pyrogenic polynuclear aromatic hydrocarbons (PAH) and synthetics (e.g., chlorinated compounds), are the major anthropogenic
residues.
Biomass combustion is another important primary source of particles injected into the global atmosphere. It contributes many
trace substances which are reactants in atmospheric chemistry and soot paniculate matter with adsorbed biomarker compounds,
most of which are unknown chemical structures. The injection of natural product organic compounds into smoke occurs primarily
by direct volatilization/steam stripping and by thermal alteration based on combustion temperature. Although the molecular
composition of organic matter in smoke particles is highly variable, the molecular tracers are generally still source specific.
Retene has been utilized as a tracer for conifer smoke in urban aerosols, but is not always detectable. Dehydroabietic acid
is generally more concentrated in the atmosphere from the same emission sources. Degradation products from biopolymers (e.g.,
levoglucosan from cellulose) are also excellent tracers. An overview of the biomarker compositions of biomass smoke types
is presented here. Defining additional tracers of thermally-altered and directly-emitted natural products in smoke aids the
assessment of the organic matter type and input from biomass combustion to aerosols. The precursor to product approach of
compound characterization by organic geochemistry can be applied successfully to provide tracers for studying the chemistry
and dispersion of ambient aerosols and smoke plumes.
Presented at the 6th FECS Conference on Chemistry and the Environment, Atmospheric Chemistry and Air Pollution, August 26–28,
1998, Copenhagen. 相似文献
177.
北京市大气细颗粒物对Balb/c 3T3细胞周期的影响 总被引:2,自引:0,他引:2
研究了北京市大气细颗粒物有机提取物 (EOC)对Balb c 3T3细胞周期及调节因子的影响 .实验发现 116 μg mL细颗粒物EOC即有明显的细胞毒性 ,抑制细胞生长 ,并存在剂量 反应关系 ,IC50 为 4 0 2 2 μg mL ;流式细胞仪分析显示 136 6 μg mLPM2 5EOC可造成细胞周期改变 ,G0 G1期、G2 M期细胞分布增加 ,分别为 16 2 4 % (P <0 0 1)与 3 17% (P <0 0 5 ) ,S期细胞分布减少 2 0 4 % (P <0 0 1) ,并伴有P5 3含量的增加 ;4 0 9 8、4 78 1μg mL的PM2 5EOC可诱导Balb c3T3细胞凋亡 .提示PM2 5有机提取物可能通过P5 3途径引起Balb c 3T3细胞周期阻滞 ,并诱导细胞凋亡 . 相似文献
178.
利用方式对紫色水稻土有机碳与颗粒态有机碳的影响 总被引:6,自引:0,他引:6
土壤是陆地生态系统中重要的动态碳库,其微小的变化可能带来对全球大气CO2浓度的较大变化。颗粒态有机碳在土壤中周转速度较快,比土壤总有机碳更易受土地利用方式的影响,对于评价土地利用变化对土壤碳固定过程影响具有重要意义。采集不同的耕作、轮作和施肥处理的14年28茬的紫色土长期试验土壤,分析有机碳与颗粒态有机碳含量在土壤及不同深度分布特点,结果表明:长期垄作免耕并实行水稻(Oryza sativa)油菜(Brassica)轮作的利用方式下,0~10cm土层土壤有机碳与颗粒态有机碳含量明显高于其他利用方式下,而稻油水旱轮作平作利用方式下最低。整个耕层0~30cm深度的土壤有机碳含量介于8.92~29.98g·kg-1之间,颗粒态有机碳含量变幅为0.54~3.43g·kg-1之间,且存在随深度递增而降低的趋势。土壤有机碳与颗粒态有机碳都可用作评价利用方式影响紫色水稻土土壤质量变化与固碳能力的有效指标,但颗粒有机碳对于管理措施的响应更为敏感。从总有机碳与颗粒有机碳的关系来看,不同管理下有机碳的增加与土壤物理保护能力的提高有关。垄作免耕(稻油)的利用方式最有利于有机碳的保护和稳定。 相似文献
179.
为了定量评价细粒子PM2.5的人体肺部暴露水平,首先,对暴露、暴露量、剂量、暴露评价等多个概念进行了明确界定,在此基础上,重点引入国际辐射防护委员会(ICRP)的人体肺部PM浓度模型对人体肺部PM2.5的浓度进行了模拟,定量化研究了广州市抽样人群PM2.5的作用剂量,作用剂量直接反映了进入人体肺部污染物的量.结果表明,广州市抽样人群平均PM2.5的作用剂量在肺部咽喉以外部分(ET)、支气管部分(BB)、肺泡空隙区(AI)分别为576.8 ̄975.9μg·d-1、357.5 ̄619.8μg·d-1、154.4 ̄290.1μg·d-1. 相似文献
180.
对太湖不同生态型湖区水体悬浮颗粒物含量,有机磷组成及降解特征进行分析,研究了富营养化湖泊颗粒磷性质及其对水体磷循环的影响.太湖颗粒P平均占水体TP浓度的75.86%;不同生态类型湖区间颗粒物性质差异明显,河口区和湖心区的颗粒物含量高于藻型湖区和草型湖区,但颗粒物有机质比例分布却相反.利用31P液相核磁共振法(31P-NMR)发现太湖悬浮颗粒P的成分包括膦酸酯,正磷酸盐,磷酸单酯,磷酸二酯,焦磷酸盐和多聚磷酸盐6类,含量分别为1.06%,50.99%,33.02%,2.48%,10.68%和3.80%.不同生态型湖区之间颗粒P组成差异明显,河口区正磷酸盐含量最高,达到82.57%,藻型湖区和湖心区颗粒有机磷比例最高,分别达到达到 64.02%和63.95%;颗粒物焦磷酸盐和多聚磷酸盐可能以藻源性颗粒物来源为分别与Chla浓度呈显著相关(P<0.05; P<0.01).颗粒态生物可利用性磷(PEHP)与正磷酸盐显著相关(P<0.05),说明颗粒物正磷酸盐是颗粒物生物可利用性磷的重要来源.太湖PEHP降解速率平均为47.3min,PEHP占水体生物可利用磷(EHP)的65.16%,说明颗粒P是水体溶解性反应磷(SRP)补充的重要来源. 相似文献