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81.
基于遗传算法的可持续土地利用动态规划 总被引:1,自引:0,他引:1
在建立和求解多目标可持续土地利用动态规划模型过程中,采用遗传算法并结合多目标模糊优选理论处理多目标土地利用结构优化问题。其详细步骤为:在分析区域特征基础上构建时间序列;通过现状分析设置土地利用类型决策变量,确定优化目标和约束条件,构建土地利用结构多目标优化模型;用灰色GM(1,1)预测模型对土地利用结构优化多目标模型参数进行预测;用遗传算法多目标优化方法对土地利用结构优化模型求解得pareto解集;最后运用多目标模糊优选动态规划方法对规划期内各时间段的pareto解集进行模糊动态优选,以最大优属度判定原则确定出最优决策序列。自贡市的实例表明,该方法有助于解决多目标协调问题,并通过提供多方案选择性,从而使规划更具灵活性,同时又便于充分吸纳公众参与,减少规划中的不确定性,增加规划的科学性、现实性和可操作性。 相似文献
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83.
Gradients of genetic distances (GGDs) between 26 adjacent cenopopulations of Scotch pine (Pinus sylvestris L.) along the transects through the distinct landscape-ecotopic isolation borders were analyzed graphically. The results
made it possible to reveal and quantitatively estimate gradients and borders of gene-pool structural patterns in populations
of this species in the central part of Northern Eurasia. In lowland areas, the most distinct borders were found between pine
populations growing on dry lands and bogs (Pineta sphagnosa) in the forest zone of the Transural region, as well as between the Arakaragaiskii and Amankaragaiskii island pine forests
in the steppe zone (Northern Turgai). In highland areas (the Urals and the Carpathians), the greatest GGDs were observed between
low-mountain (about 600 m above sea level) and middle-mountain (850–900 m) populations. Analysis of GGDs is a promising gene-geographic
method for determining population borders and studying the chorogenetic structure of species. 相似文献
84.
《International Journal of Sustainable Engineering》2013,6(2):122-137
In this research a closed loop supply chain is designed which incorporates reverse logistics and forward logistic system simultaneously. In the design of reverse logistic system, recovery options are embedded in traditional supply chain for treating returned products. The recovery system includes collection centres, remanufacturing plants and disposal centres. Since the product return is supply driven, there is an uncertainty about it. In the proposed configuration for closed loop supply chain, the optimised configuration for supply chain in terms of locating recovery plants is developed. Accordingly, a fuzzy mixed integer linear programming model develops to deal with the uncertainty of returning products by customers. A general-purpose solver (LINGO 8.0) and a Meta heuristic approach (genetics algorithm) are implemented to solve the proposed model. The answers are compared by defining indexes and then the optimal answer, configuration and variables are identified. This solution will suggest a new design of supply chain network in which waste of materials is minimised and the new raw materials are necessary only when the used products may not be recovered by recovery options. 相似文献
85.
Renal abnormalities are some of the commonest and most easily detectable anomalies on ultrasound. Many are an isolated finding but the prognosis may be altered considerably by the detection of other anomalies which could indicate a genetic disorder or syndrome. It is often easier to detect presupposed anomalies and the purpose of this article is to introduce and discuss those syndromes that may present with a renal abnormality on ultrasound. Common renal findings are presented with the range of additional anomalies that should be sought and suggested diagnostic tests. It should be remembered that although for many genetic conditions specific mutation analysis is now available, this usually requires pre‒pregnancy investigations. Furthermore, in some cases the definitive diagnosis may not be suspected until post mortem. By this time it may be too late to establish a cell line to confirm the suspicion using laboratory methods. It is therefore important to take tissue samples antenatally where possible, or at delivery, as postnatal samples may have a high culture failure rate. Copyright © 2001 John Wiley & Sons, Ltd. 相似文献
86.
Guido Pennings 《黑龙江环境通报》2002,22(12):1123-1129
The arguments against the use of preimplantation genetic diagnosis (PGD) for non-medical sex selection are analysed. It is concluded that the distinction between medical and non-medical reasons is difficult to maintain, that the disproportionality of means and end is not a decisive counterargument and that the fear of damage to the reputation of PGD does not justify the refusal of controversial applications. Moreover, since non-medical sex selection does not belong to basic health care, it should not be equally accessible to all. The position defended in this article is founded on two basic principles: (1) medical reasons have priority on non-medical reasons, and (2) personal reasons do not qualify for public funding. In order to respect both principles, it is proposed that restrictions should be installed to control the number of requests for social sexing and that a tax should be imposed on these elective services. The tax should compensate the society for the investment it made in the training and education of the physician. Copyright © 2002 John Wiley & Sons, Ltd. 相似文献
87.
The main difficulty in developing a molecular diagnosis of spinal muscular atrophy (SMA) resides in the specific genomic structure of the locus. Indeed, two highly homologous survival motor neurone genes, SMN1 and SMN2, are present at the locus. The detection of the homozygous deletion of exons 7 and 8 of the SMN1 gene, which is present in 90 to 98% of the patients, is based on methods highlighting 1 of the 8 nucleotidic mismatches existing between these 2 genes. In order to offer preimplantation genetic diagnosis (PGD) for SMA, we developed a new allele-specific amplification method. The main disadvantage of our previously described strategy resided in the possibility of diagnosing, in case of amplification failure, an unaffected embryo as affected. We present here a new PGD-SMA method. We established the conditions for three different duplex PCRs, allowing the specific detection of the SMN1 gene and one polymorphic marker, either D5S629, D5S1977, or D5S641. Of the 60 to 90 single cells tested, the PCR efficiency varied from 98 to 100% with a complete genotype obtained in a range between 81 and 87% with a global allele drop-out rate of 9%. Such a test was used to perform 1 PGD cycle for which 7 embryos could be analysed. All the embryos were fully diagnosed, six as unaffected and one as affected. Four embryos were transferred, but no pregnancy ensued. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
88.
89.
Kayoko Saito 《黑龙江环境通报》2006,26(5):415-417
Fukuyama congenital muscular dystrophy (FCMD) is characterized by infantile hypotonia, symmetrical generalized muscle weakness, and neuronal migration disturbances that result in changes consistent with cobblestone lissencephaly with cerebral and cerebellar cortical dysplasia. FCMD is recognized as an autosomal recessive genetic defect. Genetic counselling is recommended for parents at risk of having a child with FCMD. Given the high risk and overwhelming prospect of having another child with this incurable devastating condition leads many couples to consider prenatal diagnosis. In Japanese families, haplotype analysis using microsatellite markers is available. In non-Japanese families, DNA sequence analysis is available. Both disease-causing alleles of an affected family member must be identified before prenatal testing can be performed. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
90.
R. Saura W. Traore L. Taine Z. Q. Wen D. Roux B. Maugey-Laulom M. Ruffie A. Vergnaud J. Horovitz 《黑龙江环境通报》1995,15(7):609-614
Six prenatally diagnosed cases of trisomy 9 are reported and 22 previously reported cases are reviewed; the difficulty of genetic counselling for such cases and the variation in the percentage of trisomic cells in different tissues, thus making accurate diagnosis of trisomy 9 difficult, are emphasized. In addition to karyotyping results, ultrasound findings are important in achieving diagnoses. Finally, a course of action when prenatal trisomy 9 is detected is proposed. 相似文献