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421.
本文通过百花湖沉积物柱芯不同化学相磷含量分布,孔隙水地球化学及早期成岩模式和通量估算等研究,揭示了磷在早期成岩过程中迁移,转化和富集规律,揭示某些湖泊表层沉积物几厘米磷蓄积浓度的增加与磷在早期成岩过程中的行为有关。  相似文献   
422.
A scanning transmission X-ray microscope at the Lawrence Berkeley National Laboratory is used to measure organic functional group abundance and morphology of atmospheric aerosols. We present a summary of spectra, sizes, and shapes observed in 595 particles that were collected and analyzed between 2000 and 2006. These particles ranged between 0.1 and 12 μm and represent aerosols found in a large range of geographical areas, altitudes, and times. They include samples from seven different field campaigns: PELTI, ACE-ASIA, DYCOMS II, Princeton, MILAGRO (urban), MILAGRO (C-130), and INTEX-B. At least 14 different classes of organic particles show different types of spectroscopic signatures. Different particle types are found within the same region while the same particle types are also found in different geographical domains. Particles chemically resembling black carbon, humic-like aerosols, pine ultisol, and secondary or processed aerosol have been identified from functional group abundance and comparison of spectra with those published in the literature.  相似文献   
423.
Atrazine degrading enrichment culture was prepared by its repeated addition to an alluvial soil and its ability to degrade atrazine in mineral salts medium and soil was studied. Enrichment culture utilized atrazine as a sole source of carbon and nitrogen in mineral salts medium and degradation slowed down when sucrose and/or ammonium hydrogen phosphate were supplemented as additional source of carbon and nitrogen, respectively. Biuret was detected as the only metabolite of atrazine while deethylatrazine, deisopropyatrazine, hydroxyatrazine and cyanuric acid were never detected at any stage of degradation. Enrichment culture degraded atrazine in an alkaline alluvial soil while no degradation was observed in the acidic laterite soil. Enrichment culture was able to withstand high concentrations of atrazine (110 μg/g) in the alluvial soil as atrazine was completely degraded. Developed mixed culture has the ability to degrade atrazine and has potential application in decontamination of contaminated water and soil.  相似文献   
424.
Road-deposited sediment (RDS) and its associated contaminant load play a critical role in degrading receiving water bodies. Few quantitative multi-element RDS studies exist, and there are none from Hawaii. This lack of baseline data combined with concerns with high concentrations of Pb and Cu in fish and enrichment of Cu, Pb and Zn in bed sediments from Manoa Stream, Hawaii, lead to a detailed characterization of RDSs in Manoa basin. Data for a total analysis of 23 elements using inductively coupled plasma atomic-emission spectrometry and instrumental neutron activation analysis and 16 elements using a 0.5 M HCl partial leach are presented for RDSs and background soils. Concentration data, comparisons with environmental guidelines, and concentration enrichment ratios (CERs) all indicate that RDS in Manoa has a significant degree of anthropogenic pollution. The most environmentally important elements were Pb, Sb and Zn. Concentrations of these elements, primarily vehicle contributed, compare favorably with those from other studies of RDS. The high mean concentration of Pb (151 mg/kg) compared to background soils (13 mg/kg) indicates remobilization of Pb previously stored in soils and transported to road surfaces by water erosion processes. The higher Pb CER(Total) in RDSs compared to bed sediments from Manoa Stream suggests a potential link via ubiquitous storm drains and subsequent dilution with less contaminated fluvial sediments. Data from the HCl leach also support Pb and Zn as having significant anthropogenic signals, and Cu having a moderate signal. These data indicate that RDSs in Manoa basin are generally contaminated with certain potentially toxic elements and the legacy of past use of leaded gasoline is still a concern in this urban drainage system.  相似文献   
425.
厌氧菌降解四氯乙烯的研究   总被引:2,自引:0,他引:2  
报道了洳气污泥富集培养物中厌氧菌降解四氯乙烯的特征。研究结果表明,沼气污泥在甲醇、甲酸盐、乙酸盐、乙醇和H2/CO2等不同碳源基质中的富集培养物,以利用甲醇为碳源的富信培养物降解四氯乙烯(Tetrachloroe-thylene,简称PCE,下同)活性最高,平均每升培养液每天降解PCE1400nmol。经对该富集培养物的分离培养,已分离出4株厌氧细菌,其中一株为甲烷八叠球菌,两株为弧菌,一株为杆菌  相似文献   
426.
An enrichment culture was used to study atrazine degradation in mineral salt medium (MSM) (T1), MSM+soil extract (1:1, v/v) (T2) and soil extract (T3). Results suggested that enrichment culture required soil extract to degrade atrazine, as after second sequential transfer only partial atrazine degradation was observed in T1 treatment while atrazine was completely degraded in T2 and T3 treatments even after fourth transfer. Culture independent polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) technique confirmed selective enrichment of genus Bacillus along with Pseudomonas and Burkholderia. Degradation of atrazine/metabolites in the industrial wastewater was studied at different initial concentrations of the contaminants [wastewater-water (v/v) ratio: T1, 1:9; T2, 2:8; T3, 3:7; T4, 5:5 and T5, undiluted effluent]. The initial concentrations of atrazine, cyanuric acid and biuret ranged between 5.32 and 53.92 µg mL?1, 265.6 and 1805.2 µg mL?1 and 1.85 and 16.12 µg mL?1, respectively. The enrichment culture was able to completely degrade atrazine, cyanuric acid and biuret up to T4 treatment, while no appreciable degradation of contaminants was observed in the undiluted effluent (T5). Inability of enrichment culture to degrade atrazine/metabolites might be due to high concentrations of cyanuric acid. Therefore, a separate study on cyanuric acid degradation suggested: (i) no appreciable cyanuric acid degradation with accumulation of an unidentified metabolite in the medium where cyanuric acid was supplemented as the sole source of carbon and nitrogen; (ii) partial cyanuric acid degradation with accumulation of unidentified metabolite in the medium containing additional nitrogen source; and (iii) complete cyanuric acid degradation in the medium supplemented with an additional carbon source. This unidentified metabolite observed during cyanuric acid degradation and also detected in the enrichment culture inoculated wastewater samples, however, was degraded up to T4 treatments and was persistent in the T5 treatment. Probably, accumulation of this metabolite inhibited atrazine/cyanuric acid degradation by the enrichment culture in undiluted wastewater.  相似文献   
427.
为了研究进水磷限制条件下聚糖菌(GAOs)反应器模型的构建与特征,采用以厌氧-好氧运行的SBR系统,以乙酸为单一碳源,利用高通量测序技术监测了系统种群的动态变化。系统运行前140 d完全限制进水磷酸盐,140 d后进水添加1 mg·L−1(以P计)的磷酸盐作为营养盐用于微生物生长。结果表明,在进水完全进行磷限制的条件下,厌氧阶段几乎没有乙酸的吸收,同时也没有厌氧糖原消耗与PHAs合成,系统无法富集到GAOs;在进水中磷酸盐质量浓度调整为1 mg·L−1并继续运行27 d后,系统显示出典型的聚糖代谢模式,即厌氧阶段乙酸被完全吸收 、消耗了0.034 g·g−1的糖原,合成了0.041 g·g−1的PHAs。宏基因组测序结果表明,系统稳定后主要富集到Candidatus Contendobacter这类GAOs,相对丰度占系统的49.4%。污泥镜检结果表明,添加1 mg·L−1磷酸盐后污泥逐渐由松散的絮状转变为颗粒状;由絮状向颗粒状过渡阶段,污泥表面附着大量丝状菌,系统颗粒污泥的形成可能与丝状菌的大量繁殖有关。以上研究结果从微观结构揭示了进水磷限制条件下GAOs的富集过程菌群结构及污泥形态的变化,可为GAOs为主的工艺运行提供参考。  相似文献   
428.
考察了不同有机改性硅对微囊藻毒素LR(mLR)和LA(mLA)的等温吸附行为。结果表明,有机改性硅可有效吸附去除水体中<0.1×10-6(质量分数)的微囊藻毒素,并且吸附去除效果随表面改性官能团中碳原子数量的增加而增加;相同条件下,有机改性硅在微囊藻毒素异构体之间存在着一定的吸附选择性。  相似文献   
429.
喀斯特高镉地质背景区水稻镉的富集、转运特征与机理   总被引:1,自引:0,他引:1  
西南喀斯特地区土壤镉(Cd)具有\"高地质背景、低污染风险\"特征,但超过《土壤环境质量农用地土壤污染风险管控标准》风险管制值的区域是否仍具有低风险性,是迫切需要回答的问题.本文在罗甸县喀斯特峰丛谷地选择一个高Cd 土壤水稻种植区,开展土壤-水稻系统Cd含量特征和土壤Cd赋存形态等方面的研究,评价水稻各部位Cd的富集、转运...  相似文献   
430.
This study proposes the valuation of wetland functions as an alternative to the conventional approach to wetland valuation, in order to derive indicators for decision-making in wetland management. It is illustrated that these functions can be valuated in terms of the goods and services they provide to society. Using a functional approach, the functions are identified and the goods and services they provide are explicitly allocated among them; then, the latter are valuated with the Contingent Valuation method. Statistical analysis of the data provides welfare measures that reflect the value of these functions. It is argued that the values of separate functions are more useful in policy-making than their aggregated value.
Athanasios RagkosEmail: Phone: +30-2310-998826Fax: +30-2310-998828
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