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501.
对聚亚磺酰氨基酰胺(PSAA)作为新型抗氧化反渗透膜材料的可能性,以及聚合条件和成膜条件对膜性能的影响作了初步研究。 相似文献
502.
一体式膜生物反应器污水处理工艺研究 总被引:1,自引:0,他引:1
在一体式膜生物反应器研制开发实验及反应器各参数运行协调理论分析的基础上,提出了一体式膜生物反应器工艺各参数间的设计原则、方法、步骤及设计实例,对该工艺的运行能耗作了评价. 相似文献
503.
504.
Domestic wastewater was treated by combined anaerobic biofilm-aerobic membrane bioreactor(MBR) process, and part biomass in MBR was withdrawn, to treat with ozone, then the ozonated sludge was returned to anaerobic inlet. In aerobic MBR, MLSS and DO were controlled at 3000—3500 mg/L and 0.8 mg/L respectively. Comparing the experimental results of two stages, it was noticed that ozonation did not affect the removal efficiency for organics but had a significant influence on the removals of NHs-N and TN. During the ozonation period of two months, no excess sludge was wasted, and a zero sludge yield was obtained. 相似文献
505.
506.
Jon Barret Dr David Chitayat MD FABMG FCCMG Matthew Sermer Koffi Amankwah Robert Morrow Ants Toi Greg Ryan 《黑龙江环境通报》1995,15(9):849-853
The prenatal diagnosis of an echogenic fetal lung (EFL) is now often made in the early second trimester using high-resolution ultrasound. This ultrasound appearance is usually caused by a congenital cystic adenomatoid lung malformation (CCAM), an intrapulmonary lung sequestration or obstruction of a major airway. In order to provide prognostic guidelines to parents who may be considering termination of a fetus with these findings, we have analysed a series of 11 cases diagnosed in our centre over the past 2 years in conjunction with 60 cases from major published series. The data suggest that in the absence of non-immune hydrops fetalis (NIHF) or other anomalies, the outcome for the fetuses is excellent, with over 90 per cent survival. Neither early diagnosis (24 weeks) nor the presence of mediastinal shift is a poor prognostic indicator. In addition, it appears that if NIHF is absent at diagnosis, the chance that it will develop as the pregnancy continues is small (6 per cent). Furthermore, there is a significant (up to 30 per cent) chance that this ultrasound finding will resolve in utero. The development of in utero fetal surgical techniques may be the only hope for those hydropic fetuses who appear to have a dismal prognosis. 相似文献
507.
Francine Pratlong Pierre Boulot Eric Issert Martine Msika Frédéric Dupont Bruno Bachelard Pierre Sarda Jean-Louis Viala Daniel Jarry 《黑龙江环境通报》1994,14(3):191-198
One hundred and ninety women who contracted toxoplasmosis after the seventh week of pregnancy underwent antenatal diagnosis, including ultrasound examination and biological tests. Tests included Toxoplasma isolation in fetal blood and amniotic fluid by mouse inoculation, specific IgM and IgA in fetal blood, and non-specific tests. Twenty fetuses had positive specific as well as non-specific tests for Toxoplasma infection. At birth, four of these presented with clinical congenital toxoplasmosis and 12 with subclinical forms. Antenatal diagnosis enabled the detection of 83 per cent of the infected fetuses. Under specific conditions, cordocentesis permits early diagnosis and considerably reduces the number of terminations of pregnancy. 相似文献
508.
M. R. Thomas B. Tutschek A. Frost C. H. Rodeck N. Yazdani I. Craft R. Williamson 《黑龙江环境通报》1995,15(7):641-646
A single copy Y-chromosome DNA sequence was amplified using the polymerase chain reaction (PCR) from the peripheral blood of 30 women who had achieved a pregnancy through an in vitro fertilization (IVF) programme. The time of conception was known precisely and was confirmed by serial ultrasound scans. Conceptions were dated as the number of weeks after fertilization plus 2, to give a time equivalent to the obstetric menstrual dating of the pregnancy (LMP). Y-chromosome-specific DNA was detected in all pregnancies with a male fetus (18/30). The earliest detection was at 4 weeks and 5 days, and the latest at 7 weeks and 1 day. Y-chromosome-specific sequences were no longer detected in any of the male pregnancies 8 weeks after delivery. No Y-chromosome sequences were detected in any of the pregnancies where only female babies were delivered. This demonstrates that fetal DNA appears in the maternal circulation early in the first trimester, that it can be identified in all pregnancies tested by 7 weeks, that it continues to be present throughout pregnancy, and that it has been cleared from the maternal circulation 2 months after parturition. Early non-invasive prenatal diagnosis for aneuploidies and inherited disorders will be possible in all pregnancies if fetal cells can be isolated free from maternal contamination (or identified accurately in the presence of maternal cells) without problems of contamination from previous pregnancies. 相似文献
509.
In a fetus with ventricular extrasystoles a congenital aneurysm of the left ventricle was diagnosed prenatally. At 32 weeks of gestation, echocardiography showed a large apical left ventricular aneurysm with a thin, hypokinetic wall. Congestive heart failure did not occur. Prenatal and postnatal examinations did not detect the aetiology of the aneurysm, but excluded the majority of possible causes. The 2-year-old child is now asymptomatic and normally developed. Neither medication nor surgical treatment have been necessary, except for antithrombotic prophylaxis with low-dose aspirin. 相似文献
510.
The effect of Ca^2 on the removal of Alexandrium sp. LC3 under HDTMAB stress was investigated. The results showed that thetoxic effect of HDTMAB on Alexandrium sp. LC3 was significantly reduced in the presence of Ca^2 , especially under 4 mmol/L of Ca^2 .To understand the underlying mechanism, the SH group and MDA content of the cell membrane and membrane permeability weremeasured. It was found that the SH content of cell member increased, the MDA content and membrane permeability decreased whenAlexandrium sp. was treated with Ca^2 and HDTMAB complex, compared with using HDTMAB only. The data suggested that Ca^2 mightpromote HDTMAB stress resistance of Alexandrium sp. LC3 by reducing the permeability and increasing the stability of cell membrane. 相似文献