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91.
Christopher S. Davies 《Environmental management》1992,16(3):323-333
Oak wilt disease, for which there is no known cure, is one of the most destructive tree killers in the United States today.
This analysis reports on the patterns of disease transmission, along with the methods of treatment used to suppress the severity
of the pathogen's attack on trees in central Texas. The practical problems inherent in the linkage between people and their
relationship with this environmental disorder are addressed. The environmental controls implemented have application to other
areas of the United States and western Europe, where tree species are subject to infections. 相似文献
92.
ABSTRACT: Levels of nitrate and other inorganic contaminants in the drinking water of 453 Nebraska communities in 1986 were compared with health data for counties in which these communities were located. Data used included death rates per 100,000 population from heart disease, cancer, cerebrovascular disease, pneumonia and chronic lung disease, plus the rate of birth defects. Water samples from 42 communities exceeded the 0.01 mg/liter state and federal standards for selenium while 19 exceeded the 10 mg/liter NO3-N standard. Statistical analysis using Pearson's correlation coefficient method showed no significant relationship between nitrate or selenium and any of the health effects studied. Only barium, fluoride, and chromium were weakly but significantly (P<0.05) correlated to one or more of the health effects. Approximately one-third of the water samples high in NO3-N also had high levels of selenium. In some communities, the presence of nitrate also signaled the presence of barium, chromium, or arsenic. Results appear to indicate no immediate health risks related to levels of nitrate, selenium, or other inorganic contaminants in Nebraska drinking water. However, this type of statistical analysis cannot be interpreted as proving or disproving a cause and effect relationship. 相似文献
93.
Influences of organic matters of soil and water on speciation and biological utilization of selenium are discussed. Humic acid is found to be the main pool of selenium in soil and affects the bio-availability of the element in soil-plant system. Fulvic acid from drinking water inhibits the absorption of selenium taken from diet. The relationship between high content of organic matters of water and selenium deficiency on the causes of KBD could be reflected in the limited synthesis of glutathione peroxidase, which is generally stimulated by fulvic acid from drinking water. 相似文献
94.
Real-time examination of the fetal heart in 350 pregnancies has allowed a composite picture of normal fetal cardiac anatomy to be established and echocardiographic interpretation has been confirmed by anatomical studies. Two echocardiographic sections are readily obtainable and are suggested as applicable to routine scanning but the specialist nature of interpreting abnormalities is stressed. Six abnormalities have been suspected during the study and five confirmed anatomically or at cardiac catheterization. In view of the low incidence of congenital heart disease in a normal obstetric population, high risk groups should perhaps be selected for cardiac scanning at the present time. These include mothers of previously affected babies, diabetic mothers and certain abnormalities of pregnancy. Fetal ascites is particularly important, being present in three of the four proven cases of cardiac abnormality. 相似文献
95.
Pyruvate dehydrogenase (PDH) E1α subunit deficiency is an X-linked inborn error of metabolism affecting males and females with equal frequency. The diagnosis is usually based on determination of enzyme activity, although this may present difficulties in some females because of X-inactivation patterns favouring expression of the normal X chromosome. This is a particular problem for prenatal diagnosis using chorionic villus cells where normal enzyme assay results do not necessarily exclude the diagnosis and confirmatory X-inactivation analysis may be complicated by variable methylation of active and inactive X chromosomes. We describe prenatal diagnosis in two pregnancies in a family following diagnosis of a PDH E1α deficient male. The first prenatal diagnosis was performed by enzyme assay, but by the time of the subsequent pregnancy, the underlying mutation in the affected male had been identified and direct gene analysis was possible. This study highlights the limitations of diagnosis of PDH E1α deficiency based on measurement of the gene product and illustrates the need for mutation analysis in affected individuals. 相似文献
96.
Jean Mossman Elisabeth P. Young A. D. Patrick A. H. Fensom Marie Ellis P. P. Benson V. M. Der Kaloustian 《黑龙江环境通报》1983,3(4):347-350
We report the prenatal diagnosis of two fetuses with Sanfilippo disease type B. In both pregnancies there were excessive amounts of heparan sulphate in amniotic fluid and the activity of N-acetyl-α-D-glucosaminidase was undetectable in cultured amniotic fluid cells. The predictions were confirmed by enzyme assay of cultured skin fibroblasts from the aborted fetus or the affected infant. The disorder was excluded for two other pregnancies at risk and the predictions are considered to be correct because of the normal progress of the healthy children. 相似文献
97.
DetoxifyingmoniliforminingrainsandwaterZhangHong,LiJilunColegeofBiologicalSciences,ChinaAgriculturalUniversity,Beijing1000... 相似文献
98.
Tang Jiajun 《环境科学学报(英文版)》1991,3(4):29-34
Altemaria alternata were isolated from wheat seeds collected from villages in Tianshui area of Gansu Province where Kaschin-Beck disease is prevalent. TLC, IR and UV analyses of metabolic extract of A. alternata show that A. alternata produce main secondary metabolites, including alternariol, alternariol methyl ether, and tenuazonic acid.There was a significant decrease in Se-GSH-Px and SOD activities, and an acceleration in lipid peroxidation in rats fed with a diet containing metabolites produced by A. alternata. 相似文献
99.
100.
I. Ceccherini M. Lituania M. S. Cordone F. Perfumo R. Gusmano F. Callea N. Archidiacono G. Romeo 《黑龙江环境通报》1989,9(11):751-758
A pregnant woman affected with autosomal dominant polycystic kidney disease (ADPKD) had a history of an affected fetus, diagnosed by sonography at 29 weeks of pregnancy. The proband's father was also affected. DNA analysis performed on chorionic villi at 11 weeks during a second pregnancy predicted an affected fetus, and sonographic examination at 14 weeks confirmed the diagnosis. 相似文献