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161.
162.
Wilhelm P. Neumann 《Die Naturwissenschaften》1981,68(7):354-359
This field is of special interest within the organometallic chemistry, which was and still is one of the most developing areas of chemistry for twenty years. The electronic structure around the atoms of germanium, tin, and lead favors both polar and radical reactions, and a plentiful coordination chemistry, too. Modern quantum chemistry arrived at these heavy atoms and allows better understanding also of low valent species, R2M. Chiral compounds with asymmetric Sn atoms, an object aimed at since 1905, have been prepared now, and dynamic stereochemistry has been studied. Industrial use of organotins has grown quickly and includes stabilization of plastics and plant and material protection as well. Biomethylation and environmental problems open this field both to biochemists and ecologists. 相似文献
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164.
Wilhelm Kuttler 《Environmental Sciences Europe》2004,16(4):263-274
Part 2 of this article provides an overview of urban climatology and is concerned with the manifestations of selected climate elements in an urban environment, with air hygiene problems in cities and with human-biometeorological aspects of urban climatology. Initially, the structure of the urban atmosphere and urban radiation and energy balances are described. The article then deals with the urban heat island effect, the near-surface wind field, urban humidity conditions and the differences between towns and surrounding areas on the basis of examples. Planning possibilities for improving the climate in our cities are presented, together with an assessment of the effectiveness of the various measures. Finally, the role of the urban climate in the current discussion of global climate change problems is considered and placed in context on the basis of previous studies. 相似文献
165.
We investigated the phylogenetic relationships among different size groups of the pelagic microcopepod Oncaea venusta Philippi, 1843, by comparing the patterns of genetic variation of specimens collected at five locations of the Indo-West Pacific Ocean. Phylogenetic analyses were based on sequence data obtained from two DNA markers: A 310 bp fragment of the mitochondrial cytochrome b (cyt b) gene and a 480 bp fragment of the nuclear internal transcribed spacer 1 (ITS1). The cyt b sequences showed a much higher level of variation than those from ITS1, but the conclusion from both genes was concordant. Four genetic clades could be differentiated. A small- and a large-size group were unambiguously assigned to two distinct clades or lineages. Unexpectedly, the medium-sized individuals could be divided into another two different genetic clades. All four lineages were supported by high bootstrap values. The high levels of sequence divergence under sympatric conditions indicated that at least the two main groups, the large and the small one, may be assigned to different species. For the medium-size group additional morphological studies and more sensitive nuclear markers are required to clarify their taxonomic status. 相似文献
166.
Rudolf Huth Rainer Hartmann Michaela Kiesel Wilhelm Pyka Annette Stallauer 《Environmental Sciences Europe》2004,16(4):239-244
Goal and Scope
The goal of this study is the investigation and the grafic presentation of the characteristic redox zonation in a mineral oil contaminated aquifer which will be formed in the plume downstream of the contamination source. Methanogenic conditions, sulfate-reduction, Fe(III)-reduction, Mn(IV)-reduction, nitrate-reduction, aerobic conditions. By that indications type and degree of microbial degradation which is the most important part in Natural Attenuation (NA) processes can be obtained easily.Methods
Changes of the groundwater parameters Eh, O2, NO 3 ? , SO4 2?, Fe2+, Mn2+, HCO3 ?, Ca2+ will be measured upstream, downstream and also in the centre of the plume. The results will be presented in a sequence of special diagrams.Results and Conclusion
When microbial degradation of hydrocarbons takes place, a microbial community will always use that electron acceptor from which it will gain a maximum of energy by the corresponding redox-reactions. This means as long as oxygen is available this will be used. After its depletion nitrate serves as electron acceptor leading via nitrite to the formation of nitrogen or ammonia. Manganese (IV) and Iron (III) species which are rather insoluble are mainly available from the soil-phase, can act as electron acceptor as next, leading to soluble Manganese (II) and Iron (II) compounds in groundwater. Finally before methanogenic conditions occur sulphate will become a suitable electron acceptor leading to the formation of hydrogen sulphide. All these processes of mineralization of the hydrocarbons will lead to the production of CO2 and as consequence to an increase of HCO3 ? in groundwater changing the calcareous/carbonic acid-equilibrium. By that more soluble Ca(HCO3)2 is formed from insoluble CaCO3, so the concentration from Ca2+ will also inerease. Thus, by the action of microorganisms, a typical redox-zonation and changes of other parameters will occur.Recommendations and Perspective
To follow the changes in time and space of some characteristic groundwater parameters is a simple way to estimate the potential of microbial degradation in a contaminated aquifer considering Natural Attenuation (NA)-processes. 相似文献167.
A gas chromatographic method for the determination of the insecticides acephate, dimethoate, methamidophos and omethoate in small amounts of nectar has been developed. By the use of a miniaturized extraction technique and a nitrogenphosphorus selective detector (NPD) residues down to 0.005 – 0.01 ppm could be detected in a sample size of 1 g. Because of the low content of co-extractives in nectar and the use of a highly selective detector a clean-up of the extracts was not necessary. 相似文献
168.
The use of the gasoline additive methyl tert-butyl ether (MTBE) has caused serious concern about groundwater and surface water contamination. The behavior of MTBE in the two most relevant compartments, surface water and air in a generic environment and in a simulated German environment is investigated using the equilibrium criterion (EQC) model. Due to lack of literature data, the half-life time of MTBE in river water is estimated to about 80-120 d (105 d) at 18 degrees C and roughly 1.5 a (year)(533 d) at 4 degrees C from a batch experiment. The EQC model considers four compartments, air, surface water, soil and sediment in an environment of typically 100,000 km2 with about 10% of the area covered with water. The user can progress through the tiered sequence of Level I to III with increasing complexity which reveals more information about the the fate of the considered chemical. The equilibrium mass distribution of MTBE calculated with the Level I model shows that 87% partitions into air and 13% into surface water at 10 degrees C. The results of the Level II calculations indicate that 50% of MTBE in the air is transported from the system and 38% in the air is degraded at 10 degrees C. The resulting total persistence time of 3 d for MTBE in the generic environment of the Level II model can be compared to the calculated value for chlorobenzene. The MTBE input into water is significantly more sensitive to the 'mode of entry' than input into air. The MTBE concentration in surface water is almost exclusively the result of direct emission into water, whereas the atmosphere can additionally be loaded by volatilization from water. The total aquatic MTBE emission in Germany and the average MTBE concentration in German surface waters were roughly estimated to 20-80 t a(-1) (tons per year)(50 t a(-1)) and 50 ng L(-1), respectively. Surface water concentrations calculated with the underlying assumptions of the model can neither be explained by exposure through waste water and industrial effluents nor with an estimated loss of industrially used MTBE in Germany. For the year-round scenario at 10 degrees C, MTBE concentrations of 19 ng L(-1) (surface water) and 167 ng m(-3) (air) result. However, it remains unclear whether the assumptions of the model, the lack of analyses from industrial effluents or both are responsible for the difference. Additional aquatic emission sources could result from gasoline transport on and storage near rivers. The comparison of winter and summer scenarios shows that in summer, atmospheric (25%) and aqueous (50%) concentrations are lower than in winter due to higher degradation rates. 相似文献
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170.