全文获取类型
收费全文 | 11323篇 |
免费 | 79篇 |
国内免费 | 83篇 |
专业分类
安全科学 | 283篇 |
废物处理 | 500篇 |
环保管理 | 1430篇 |
综合类 | 2459篇 |
基础理论 | 2556篇 |
环境理论 | 5篇 |
污染及防治 | 2951篇 |
评价与监测 | 684篇 |
社会与环境 | 562篇 |
灾害及防治 | 55篇 |
出版年
2022年 | 91篇 |
2021年 | 96篇 |
2019年 | 69篇 |
2018年 | 149篇 |
2017年 | 130篇 |
2016年 | 222篇 |
2015年 | 172篇 |
2014年 | 243篇 |
2013年 | 820篇 |
2012年 | 304篇 |
2011年 | 427篇 |
2010年 | 337篇 |
2009年 | 395篇 |
2008年 | 428篇 |
2007年 | 491篇 |
2006年 | 430篇 |
2005年 | 352篇 |
2004年 | 367篇 |
2003年 | 373篇 |
2002年 | 332篇 |
2001年 | 428篇 |
2000年 | 312篇 |
1999年 | 205篇 |
1998年 | 115篇 |
1997年 | 123篇 |
1996年 | 108篇 |
1995年 | 154篇 |
1994年 | 148篇 |
1993年 | 123篇 |
1992年 | 130篇 |
1991年 | 149篇 |
1990年 | 119篇 |
1989年 | 127篇 |
1988年 | 132篇 |
1987年 | 114篇 |
1986年 | 83篇 |
1985年 | 99篇 |
1984年 | 124篇 |
1983年 | 125篇 |
1982年 | 123篇 |
1981年 | 97篇 |
1980年 | 93篇 |
1979年 | 106篇 |
1978年 | 89篇 |
1977年 | 84篇 |
1976年 | 78篇 |
1975年 | 90篇 |
1974年 | 101篇 |
1972年 | 69篇 |
1965年 | 74篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
521.
Pasan Samarasin Brian J. Shuter Stephen I. Wright F. Helen Rodd 《Conservation biology》2017,31(1):126-135
Accurate understanding of population connectivity is important to conservation because dispersal can play an important role in population dynamics, microevolution, and assessments of extirpation risk and population rescue. Genetic methods are increasingly used to infer population connectivity because advances in technology have made them more advantageous (e.g., cost effective) relative to ecological methods. Given the reductions in wildlife population connectivity since the Industrial Revolution and more recent drastic reductions from habitat loss, it is important to know the accuracy of and biases in genetic connectivity estimators when connectivity has declined recently. Using simulated data, we investigated the accuracy and bias of 2 common estimators of migration (movement of individuals among populations) rate. We focused on the timing of the connectivity change and the magnitude of that change on the estimates of migration by using a coalescent‐based method (Migrate‐n) and a disequilibrium‐based method (BayesAss). Contrary to expectations, when historically high connectivity had declined recently: (i) both methods over‐estimated recent migration rates; (ii) the coalescent‐based method (Migrate‐n) provided better estimates of recent migration rate than the disequilibrium‐based method (BayesAss); (iii) the coalescent‐based method did not accurately reflect long‐term genetic connectivity. Overall, our results highlight the problems with comparing coalescent and disequilibrium estimates to make inferences about the effects of recent landscape change on genetic connectivity among populations. We found that contrasting these 2 estimates to make inferences about genetic‐connectivity changes over time could lead to inaccurate conclusions. 相似文献
522.
J. W. Wladimiroff M.D. Ph.D. M. F. Niermeijer J. J. Van Der Harten P. A. Stewart F. G. A. Versteegh W. Blom J. G. M. Huijmans 《黑龙江环境通报》1985,5(1):47-52
Congenital hypophosphatasia is an autosomal recessive disorder, which usually has a fatal outcome during the neonatal period. This report presents the prenatal diagnosis of hypophosphatasia at 16 weeks of gestation. The characteristic ultrasonic findings in this abnormality demonstrate the superiority of ultrasound as compared with radiography. 相似文献
523.
Dr E. Vamos D. Pratola N. Van Regemorter M. Freund J. Flament-Durand F. Rodesch 《黑龙江环境通报》1985,5(3):209-214
Amniocentesis was performed in view of a paternal balanced chromosomal rearrangement t(4;20)(p16;p12), inv(18)(p11q11). The pregnancy was complicated by severe oligohydramnios. The fetal karyotype was unbalanced: 46XX, der(4), t(4;20)(p16;p12), inv(18) (p11q11)pat., thus resulting in partial trisomy 2Op and monosomy 4p. In addition, the amniotic fluid alpha-fetoprotein (AFP) became increasingly elevated with gestational age. The pregnancy was terminated at 25 weeks. The fetus presented with typical facial dysmorphic features, unilateral cleft lip and palate, severe renal hypoplasia, consistent with the 4p- (Wolf-Hirschhorn) syndrome. 相似文献
524.
C. Marchese M.D. E. Savin E. Dragone F. Carozzi M. De Marchi M. Campogrande G. C. Dolfin G. Pagliano E. Viora A. Carbonara 《黑龙江环境通报》1985,5(3):221-227
Six cases of cystic hygromas detected during second trimester ultrasound examination are reported: 4 fetuses (67 per cent) had a 45, X karyotype, 1 fetus had trisomy 18, 1 fetus had a normal karyotype (46,XX) and at autopsy multiple anomalies were observed. In the latter case the family history suggested an autosomal recessive pattern of inheritance. In order to reach a definite diagnosis and give proper genetic counselling when a fetus is found to have cystic hygroma, a fetal karyotype as well as a family and reproductive history should be obtained. 相似文献
525.
526.
527.
528.
529.
530.