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481.
Guided group discussion ( [Lewin et?al., 1952], [Werner, 2003] and [Werner and Adams, 2001]) was used to persuade groups to replace their toxic home and garden chemicals with nontoxic alternatives. We hypothesized that discussion would allow participants to hear others endorse the new information, and this normative information would facilitate persuasion. Approximately two months after the group discussion, we obtained questionnaires from the organizer of the meeting and a member of the group who had missed the meeting because of another obligation (i.e., not because of disinterest in the topic). Most organizers were female and analyses were limited to females. This quasi-experimental matched control group design indicated that those who attended the meeting were more favorable towards using nontoxics and more interested in sharing leftover toxic products with friends (instead of discarding them). Path and mediation analyses showed that the organizer’s evaluation of the meeting predicted her final attitude, and perceptions that the group endorsed the material (perceived group norm) partially mediated this relationship. A second mediation analysis showed that evaluation of the meeting predicted intention to share leftover toxics and this relationship was fully mediated by the organizer’s impression that the group would also share leftovers. The results support the idea that persuasion is based both on individual evaluation and normative influence, especially when people are not confident others will accept the behavior, such as sharing leftover toxic products.  相似文献   
482.
Given the excessive use pressure on forests, characterisation of the major users of forest resources can help guide conservation efforts. This study examines whether socio-economic variables explain domestic wood use in an area of Atlantic forest in the community of Três Ladeiras (Pernambuco, north-east Brazil). Socio-economic data were collected from 62 households, and geometric measurements of wood products in each household were taken to calculate the wood volume. An informant in each household indicated the average replacement time for each type of wood use. Data were analysed for static volume (wood volume found at the time of the visit) and dynamic volume (rate of wood consumption, calculated as the ratio between volume and replacement time). Multiple regression analyses were performed to determine the relationships between wood volume (static and dynamic) and the number of species used; independent variables including monthly family income, number of residents, average age of heads of the household, age of oldest household member, average residence time of heads of the household, average education level of heads of the household and education level of the most educated household member. Monthly income was inversely related to the static wood volume (adjusted R 2 = 17.6%, p < 0.001), rate of wood consumption (adjusted R 2 = 23.0%, p < 0.001) and number of species used (adjusted R 2 = 22.3%, p < 0.001) and was the most important predictive variable for these three outcomes. Other factors such as average education level and average age of heads of the household were also explanatory variables of the total rate of wood consumption, as these two variables, together with monthly family income, explain 31.3% of the total dynamic volume. Given the high importance of income in our study, we suggest that future conservation strategies give special attention to the poorest members of the community.  相似文献   
483.
养殖池塘生态系统中磷的收支及解磷微生物的研究进展   总被引:2,自引:0,他引:2  
综述了池塘养殖系统磷的收支情况.研究发现,在池塘养殖系统中,磷输出最主要的形式为底泥沉积,养殖池塘中存在着磷的总体利用效率不高,水体中活性磷含量低的问题.而解磷微生物的应用在一定程度上可有效解决上述问题,它们能将植物难以吸收利用的磷转化为可吸收利用的形态.通过阐述解磷微生物的种类、解磷效果及解磷机制,结合养殖池塘的情况,分析了将解磷微生物应用于水产养殖中的可行性,并对今后的研究方向作出了展望.结合我国水产养殖的实际情况,筛选适应池塘养殖环境的高效解磷微生物,并将其应用于池塘养殖中,使池塘沉积物中难溶性磷转化具备相当的可行性.  相似文献   
484.
基于虹膜识别的肉类食品可追溯系统研究   总被引:6,自引:3,他引:6  
为了加强食品安全管理,提高肉类食品溯源准确性的目的,首先提出肉类食品溯源体系的3个基本要素,认为:动物个体识别是肉食品质量控制的重要环节;采用虹膜识别作为大型动物个体识别的关键技术;解决了其他动物识别系统中的欺骗以及设备功能异常现象等问题。以奶牛为例,讨论人眼虹膜识别技术应用于大型动物识别在图像采集、虹膜定位、特征提取3方面存在的技术难点;给出了实现动物虹膜识别的技术路线;最后构建了基于虹膜识别的肉食品可追溯系统。通过详细功能划分和流程设计,为虹膜技术在肉食品可追溯系统中的应用实施提供了参考。  相似文献   
485.
Brausch JM  Rand GM 《Chemosphere》2011,82(11):1518-1532
Considerable research has been conducted examining occurrence and effects of human use pharmaceuticals in the aquatic environment; however, relatively little research has been conducted examining personal care products although they are found more often and in higher concentrations than pharmaceuticals. Personal care products are continually released into the aquatic environment and are biologically active and persistent. This article examines the acute and chronic toxicity data available for personal care products and highlights areas of concern. Toxicity and environmental data were synergized to develop a preliminary hazard assessment in which only triclosan and triclocarban presented any hazard. However, numerous PCPs including triclosan, paraben preservatives, and UV filters have evidence suggesting endocrine effects in aquatic organisms and thus need to be investigated and incorporated in definitive risk assessments. Additional data pertaining to environmental concentrations of UV filters and parabens, in vivo toxicity data for parabens, and potential for bioaccumulation of PCPs needs to obtained to develop definitive aquatic risk assessments.  相似文献   
486.
We report results of air monitoring started due to the recent natural catastrophe on 11 March 2011 in Japan and the severe ensuing damage to the Fukushima Dai-ichi nuclear reactor complex. On 17-18 March 2011, we registered the first arrival of the airborne fission products 131I, 132I, 132Te, 134Cs, and 137Cs in Seattle, WA, USA, by identifying their characteristic gamma rays using a germanium detector. We measured the evolution of the activities over a period of 23 days at the end of which the activities had mostly fallen below our detection limit. The highest detected activity from radionuclides attached to particulate matter amounted to 4.4 ± 1.3 mBq m−3 of 131I on 19-20 March.  相似文献   
487.
Explicit expressions for the end-of-life flows (EOL) of single and multiple cycle products (MCPs) are presented, including deterministic and stochastic EOL exit. The expressions are given in terms of the physical parameters (maximum lifetime, T, annual cycling frequency, f, number of cycles, N, and early discard or usage loss). EOL flows are also obtained for hi-tech products, which are rapidly renewed and thus may not attain steady state (e.g. electronic products, passenger cars). A ten-step recursive procedure for obtaining the dynamic EOL flow evolution is proposed. Applications of the EOL expressions and the ten-step procedure are given for electric household appliances, industrial machinery, tyres, vehicles and buildings, both for deterministic and stochastic EOL exit, (normal, Weibull and uniform exit distributions). The effect of the physical parameters and the stochastic characteristics on the EOL flow is investigated in the examples: it is shown that the EOL flow profile is determined primarily by the early discard dynamics; it also depends strongly on longevity and cycling frequency: higher lifetime or early discard/loss imply lower dynamic and steady state EOL flows. The stochastic exit shapes the overall EOL dynamic profile: Under symmetric EOL exit distribution, as the variance of the distribution increases (uniform to normal to deterministic) the initial EOL flow rise becomes steeper but the steady state or maximum EOL flow level is lower. The steepest EOL flow profile, featuring the highest steady state or maximum level, as well, corresponds to skew, earlier shifted EOL exit (e.g. Weibull). Since the EOL flow of returned products consists the sink of the reuse/remanufacturing cycle (sink to recycle) the results may be used in closed loop product lifecycle management operations for scheduling and sizing reverse manufacturing and for planning recycle logistics. Decoupling and quantification of both the full age EOL and of the early discard flows is useful, the latter being the target of enacted legislation aiming at increasing reuse.  相似文献   
488.
The 2,3,3′,4,4′,5,5′-heptachloro-1′-methyl-1,2′-bipyrrole (Q1, MBP-79) and further halogenated 1′-methyl-1,2′-bipyrroles (MBPs) are a class of marine natural products repeatedly detected in seafood and marine mammals from all over the world. Only Q1 is currently commercially available as reference standard and the full synthesis of mixed brominated-chlorinated compound is rather complicated. For this reason, synthetic Q1 (240 mg) was transferred into bromine-containing MBPs by UV-irradiation in the presence of bromine. Bromine, which rapidly vanished from the solutions, was re-newed during the reaction in order to generate higher amounts of Br-containing MBPs. A total of ∼150 mg Q1 was transferred after ∼10 min irradiation with high amounts of Br2 to give 30.5 mg BrCl6-MBPs along with lower proportions of Br2Cl5-, Br3Cl4-, Br4Cl3- and traces of Br5Cl2-MBPs. Longer UV-irradiation in the presence of Br2 even allowed for the detection of Br6Cl-MBPs and traces of Br7-MBP. However, this reaction also provided some unknown by-products. A sample stored in the dark and later in in-door light (no UV irradiation) also eliminated Q1 after 76 d in favour of heptahalogenated MBPs with up to three bromine substituents. The irradiation products were separated on silica, and fractions containing only Q1 and BrCl6-MBPs were then further fractionated by non-aqueous RP-HPLC. A pure isolate of the major BrCl6-MBP (∼1.5 mg) was characterized by GC/MS and 13C NMR to be 2-bromo-3,3′,4,4′,5,5′-hexachloro-1-methyl-1,2′-bipyrrole (Br-MBP-75). Partial GC enantioseparation of the axially chiral Br-MBP-75 was achieved on a β-PMCD column. A full enantioseparation was managed by enantioselective HPLC using a NUCLEOCEL DELTA S column. Low amounts of pure BrCl6-MBP enantiomers could be trapped.  相似文献   
489.
Müller A  Schulz W  Ruck WK  Weber WH 《Chemosphere》2011,85(8):1211-1219
Non-target screening via high performance liquid chromatography-mass spectrometry (HPLC-MS) has gained increasingly in importance for monitoring organic trace substances in water resources targeted for the production of drinking water. In this article a new approach for evaluating the data from non-target HPLC-MS screening in water is introduced and its advantages are demonstrated using the supply of drinking water as an example. The crucial difference between this and other approaches is the comparison of samples based on compounds (features) determined by their full scan data. In so doing, we take advantage of the temporal, spatial, or process-based relationships among the samples by applying the set operators, UNION, INTERSECT, and COMPLEMENT to the features of each sample. This approach regards all compounds, detectable by the used analytical method. That is the fundamental meaning of non-target screening, which includes all analytical information from the applied technique for further data evaluation. In the given example, in just one step, all detected features (1729) of a landfill leachate sample could be examined for their relevant influences on water purification respectively drinking water. This study shows that 1721 out of 1729 features were not relevant for the water purification. Only eight features could be determined in the untreated water and three of them were found in the final drinking water after ozonation. In so doing, it was possible to identify 1-adamantylamine as contamination of the landfill in the drinking water at a concentration in the range of 20 ng L−1. To support the identification of relevant compounds and their transformation products, the DAIOS database (Database-Assisted Identification of Organic Substances) was used. This database concept includes some functions such as product ion search to increase the efficiency of the database query after the screening. To identify related transformation products the database function “transformation tree” was used.  相似文献   
490.
Transformation products usually differ in environmental behaviors and toxicological properties from the parent contaminants, and probably cause potential risks to the environment. Toxicity evolution of a labile preservative, bronopol, upon primary aquatic degradation processes was investigated. Bronopol rapidly hydrolyzed in natural waters, and primarily produced more stable 2-bromo-2-nitroethanol (BNE) and bromonitromethane (BNM). Light enhanced degradation of the targeted compounds with water site specific photoactivity. The bond order analysis theoretically revealed that the reversible retroaldol reactions were primary degradation routes for bronopol and BNE. Judging from toxicity assays and the relative pesticide toxicity index, these degradation products (i.e., BNE and BNM), more persistent and higher toxic than the parent, probably accumulated in natural waters and resulted in higher or prolonging adverse impacts. Therefore, these transformation products should be included into the assessment of ecological risks of non-persistent and low toxic chemicals such as the preservative bronopol.  相似文献   
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