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Joe C. Rutledge Arthur G. Weinberg Jan M. Friedman Mary Jo Harrod Rigoberto Santos-Ramos 《黑龙江环境通报》1986,6(1):51-61
In utero sonographic diagnoses from forty-five malformed infants were correlated with their autopsy findings. Fifty-two malformations were diagnosed prenatally in 42 of the patients but 90 additional malformations were not. Nine sonographically diagnosed abnormalities were not confirmed at autopsy. Factors compromising sonographic diagnosis included: limited examinations, small fetal size, timing of examination, oligohydramnios, fetal position, nature of the malformation and unfamiliarity of the ultrasonographer with specific malformation syndromes. In vitro ultrasonography is an invaluable tool of diagnosing congenital malformations but has limitations. 相似文献
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A requirement for geostatistical prediction is estimation of the variogram from the data. Often low sample size is a major impediment to elucidating a variogram even for a highly autocorrelated spatial process. This paper presents a methodology for improving variogram estimation when samples exist from multiple years or regions sharing a similar process for generating spatial autocorrelation. Such samples may come from annual monitoring programs for natural resources or from multiple geologic regions. As each set of samples contains some information on the spatial autocorrelation, combining information through the construction of a combined variogram cloud and binning to obtain a common variogram improves the estimation of the variogram. In both simulations and in real datasets of oyster abundance the method proposed here reduces the likelihood of failing to obtain a variogram from a set of samples and improves the efficiency of variogram estimation. In practice, the benefits obtained by estimating an otherwise elusive variogram generally outweigh the costs of using a slightly incorrect variogram model if different sampling stanzas are combined when they do not share the same spatial autocorrelation. Copyright © 2007 John Wiley & Sons, Ltd. 相似文献
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Ariamalar Selvakumar Mary Ellen Tuccillo Swarna Muthukrishnan Asim B. Ray 《补救:环境净化治理成本、技术与工艺杂志》2009,19(2):135-142
Several compositions of Fenton's Reagent and hydrogen peroxide alone were used to disinfect combined sewage samples from a wastewater treatment facility. The presettled samples contained suspended solids (SS) and dissolved organic carbon (DOC) at concentrations of 28 and 290 mg/L, respectively. Disinfection with Fenton's Reagent was carried out at a pH between 5.90 and 6.0 and at a temperature of 25°C. All disinfected samples contained residual oxidants. Under all reaction conditions studied, complete inactivation of E. coli was achieved within one minute of the addition of Fenton's Reagent. Disinfection with hydrogen peroxide alone under similar conditions is incomplete even under much longer contact times. © 2009 Wiley Periodicals, Inc. 相似文献
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A wide spectrum of genetic causes may lead to nonimmune hydrops fetalis (NIHF), and a thorough phenotypic and genetic evaluation are essential to determine the underlying etiology, optimally manage these pregnancies, and inform discussions about anticipated prognosis. In this review, we outline the known genetic etiologies of NIHF by fetal organ system affected, and provide a systematic approach to the evaluation of NIHF. Some of the underlying genetic disorders are associated with characteristic phenotypic features that may be seen on prenatal ultrasound, such as hepatomegaly with lysosomal storage disorders, hyperechoic kidneys with congenital nephrosis, or pulmonary valve stenosis with RASopathies. However, this is not always the case, and the approach to evaluation must include prenatal ultrasound findings as well as genetic testing and many other factors. Genetic testing that has been utilized for NIHF ranges from standard chromosomal microarray or karyotype to gene panels and broad approaches such as whole exome sequencing. Family and obstetric history, as well as pathology examination, can yield additional clues that are helpful in establishing a diagnosis. A systematic approach to evaluation can guide a more targeted approach to genetic evaluation, diagnosis, and management of NIHF. 相似文献
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With improvements in early diagnosis and management of genetic diseases, more women with genetic disorders are reaching reproductive age and becoming pregnant. While pregnancy can have a significant impact on a woman's health when there is an underlying genetic disorder, there can also be fetal effects, including embryopathy, fetal growth restriction, and brain injury. Some maternal genetic disorders are associated with adverse perinatal outcomes, including a high risk of perinatal loss and preterm birth. In this article, we review several maternal genetic disorders associated with fetal risk that are important for clinicians and patients to understand and manage appropriately. These include phenylalanine hydroxylase (PAH) deficiency and other inborn errors of metabolism, tuberous sclerosis complex, myotonic dystrophy, cystic fibrosis, Turner syndrome, sickle cell disease, and connective tissue disorders. 相似文献