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401.
Fetal urinary insulin-like growth factor I and binding protein 3 in bilateral obstructive uropathies
L. Bussieres K. Laborde J. C. Souberbielle F. Muller M. Dommergues C. Sachs 《黑龙江环境通报》1995,15(11):1047-1055
Fetal urinary concentrations of insulin-like growth factor I (UIGF-I) and binding protein 3 (UIGFBP-3) were determined in patients with prenatal diagnosis of bilateral obstructive uropathy. Patients were retrospectively assigned to three groups, on the basis of outcome: group 1, termination of pregnancies (n = 11) with sonographic evidence of severe oligohydramnios or renal dysplasia, confirmed at histological examination; group 2, patients (n = 10) with postnatal plasma creatinine > 50 μmol/1 at the age of 1 year (1 yr-pCreat); and group 3, patients (n = 16) with 1 yr-pCreat ≤ μmol/1. The results show a significant increase in UIGF-I and UIGFBP-3 in groups 1 (18 159 ± 9083 pg/ml; 2657 ± 669 ng/ml) and 2 (1574 ± 847 pg/ml; 176 ± 50 ng/ml) in comparison with group 3 (35 ± 6 pg/ml; 21 ± 2 ng/ml). UIGF-I and UIGFBP-3 were significantly correlated with postnatal plasma creatinine, and were both sensitive (90 per cent; 80 per cent) and specific (88 per cent; 88 per cent) for prediction of elevated 1 yr-pCreat (>50 μmol/1). Fetal urinary IGF-I and IGFBP-3 are increased in severe fetal bilateral obstructive uropathy, possibly reflecting tubular dysfunction or/and increased synthesis consequent upon fetal kidney injury. Their predictive value for postnatal renal function needs further assessment. 相似文献
402.
通过两季马铃薯大田试验,研究了嗪草酮在灌溉沙壤土中的消失和移动情况。结果表明,表层土壤中,嗪草酮施用后最初7~15天内其含量急剧降低,此后随时间推移降低幅度平缓,1993年和1994年试验结束时的残留量分别为5.9μg/kg和2.3μg/kg。两年共采集的379个土样(分布在15~75cm各土层)中只有5个检测到有嗪草酮。1994年大田135cm土层处的水样中,嗪草酮的检测率高达66%,检测浓度范围为0.06~15.85μg/kg,平均浓度为1.94μg/kg。相比较,嗪草酮在大田试验中的消失速率远大于实验室控制条件下的降解速率。 相似文献
403.
An amniocentesis was performed at 13.3 weeks' gestation for advanced maternal age. A mosaic sex chromosome pattern was found: of 50 cells examined, 34 had a 45,X karyotype. In 14 cells with a modal number of 46, a recognizable Y was substituted by a small non-fluorescent marker. C-banding identified the marker as an isodicentric in 12 cells. In two cells, the non-fluorescent marker appeared to be monocentric and looked like a non-fluorescent del (Yq), but could have been an isodicentric Y with inactivation of one of the centromeres. Two cells with a modal number of 47 showed two copies of the monocentric marker. Fluorescent in situ hybridization with an alpha satellite Y-specific centromeric probe confirmed the Y-chromosome origin of the markers and allowed for more accurate prenatal diagnostic information. 相似文献
404.
Prenatal diagnosis in a pregnancy at risk for a juvenile B1 variant of GM2-gangliosidosis was carried out. The biochemical study of the cultured amniocytes and the affected fetal brain is reported. The results obtained show that the sulphated artificial substrate can be used in the diagnosis of B1 variant, but not the neutral one. The accumulation of GM2-ganglioside in the fetal brain of the B1 juvenile form and an infantile form of GM2-gangliosidosis (0 variant) was compared. 相似文献
405.
Foci of calcification were observed at autopsy in the liver of a fetus with complete trisomy 9 on which two cordocenteses had been performed. It is suggested that liver calcifications are a possible complication of the procedure. As several other cases of calcifications in the liver and other organs of fetuses with autosomal trisomies have been described without a history of cordocentesis, further studies should be carried out to determine whether fetuses with chromosomal anomalies are more prone to thrombus formation and embolization. 相似文献
406.
407.
408.
Catherine Potvin Petra Tschakert Frédéric Lebel Kate Kirby Hector Barrios Judith Bocariza Jaime Caisamo Leonel Caisamo Charianito Cansari Juan Casamá Maribel Casamá Laura Chamorra Nesar Dumasa Shira Goldenberg Villalaz Guainora Patrick Hayes Tim Moore Johana Ruíz 《Mitigation and Adaptation Strategies for Global Change》2007,12(8):1341-1362
This paper is part of a two-year study to investigate the feasibility of initiating a Clean Development Mechanism (CDM) project
in an indigenous community of Eastern Panamá, Ipetí-Emberá. We use participatory mapping and matrices as well as household
surveys to develop a land-use/land-cover baseline scenario and examine the role of local participation in assessing land-use
change. In Ipetí, land-use change has not occurred in a linear way over the last decades, and our data unveils socio-economic
factors as potential key drivers of change. The concordance that we observed between geographic information and individual
and collective perceptions of land-use change substantiates the possibility of using local knowledge in the establishment
of baseline data for CDM projects. Our calculations suggest that the total carbon (C) stocks in the Tierra Colectiva (TC) of Ipetí-Emberá in 2004 represents a 47% reduction from the estimated C stock at the onset of settlement in the early
1970’s. Results from the participatory assessments predict that, in 2024 and in absence of a CDM project, the C stocks will
decline from 301,859 t C in 2004 to 155,730 t C, which constitutes a reduction of 52%. The scenario with CDM estimates C stocks
of 305,853 t C for 2024, a value slightly superior to the 2004 value. In the TC there is ground to believe that cattle ranching
is likely to become an ever more important activity as the population is young and growing and cannot easily move elsewhere.
Forests tend to be cleared for cultivation while pastures are established on short fallows. Our baseline scenario underlines
the potential for a CDM project to make a significant difference in the future C stocks of this landscape. 相似文献
409.
M. Schwartz M. Super J. Schmidtke C. Buys M. Farrall D. Halley M. Krawczak J. E. Poncin D. Loukopoulos M. Devoto 《黑龙江环境通报》1988,8(8):619-624
This paper presents data collected in Europe on 107 prenatal diagnoses of cystic fibrosis (CF) using linked DNA markers. To date, 38 children have been born without CF, as predicted, demonstrating the present rapid move from research to clinical genetic service. 相似文献
410.
At 10 weeks' gestation, chorionic villus biopsy was obtained from a woman at risk for Sanfilippo type C disease. Acetyl-CoA: α-glucosaminide N-acetyltransferase activity was markedly deficient. The pregnancy was terminated at 12 weeks' gestation and follow-up study on fetal fibroblasts confirmed the diagnosis. 相似文献