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41.
Twelve second-trimester fetuses with cystic hygroma underwent fetal blood sampling for rapid karyotyping, haematologic evaluation, and blood gas analysis. An abnormal karyotype was found in seven cases: monosomy X in five, trisomy 21 in one, and trisomy 13 in the other. Eight often fetuses undergoing blood gas analysis showed hypoxaemia, five of which were growth-retarded. Nine pregnancies were terminated. Of the remaining three, only one fetus survived the perinatal period.  相似文献   
42.
地震观测数据受各种周期性因素影响,其动态曲线表现为周期性变化特征,是大小不同的周期和非周期因素相互作用的结果。利用MATLAB工具包,编程幅频分析和滤波程序,以福州乌鸦咀泉水电导率的模拟观测数据为例,对其幅频谱特征和震例进行初步探讨。  相似文献   
43.
在环境空气监测点位优化中,为反映优化后点位的整体代表性,需要在允许的测定误差内以最少的测点反映区域内较长时期的整体污染水平、污染分布状况和污染趋势.本文以博山城区为例,利用地理变异系数法和Fisher最优分割法对所布设点位进行数理统计.该方法使用简便,分级自然,避免了诸多人为因素的影响,同时,优选结果具有较强的整体代表性.  相似文献   
44.
笔者自行开发并研制了低空( < 1 km) 分层降水和云水采集系统,该系统成功地应用于福建省厦门市和贵州省贵阳市酸性降水来源和成因的研究中,取得了显著的成果,为探讨酸性降水来源和成因提供了有效的技术手段和支持。该系统可以在一定程度上代替航空测量,目前国内外的类似研究中没有使用该系统进行样品采集的先例,因此该系统的开发填补了国内外相关研究领域的空白  相似文献   
45.
Multiple placental passes during chorionic villus sampling (CVS) increase the risk of fetal loss; however, specific factors that predispose to repeat aspiration have not been delineated. To identify anatomic and technical variables associated with multiple-pass procedures, a detailed review of 205 videotaped CVS procedures (single pass = 163; multiple pass = 42) was performed, blinded to pregnancy outcome. The route of sampling did not influence the need for multiple aspiration attempts (transabdominal—30/ 135; transcervical—12/70), nor was placental location alone discriminatory. However, the combination of a posterior placenta and uterine retroversion was observed more frequently in the multiple-pass cohort (8/42 vs. 9/163; p<0.05). In transabdominal cases, suboptimal needle placement (e.g., perpendicular to the placental long axis) was more common in the initial aspiration of a multiple-pass procedure (21/30 vs. 38/105;p<0.01), while limited penetration of the catheter tip (e.g., just inside the placental edge) characterized a majority of multiple-pass cases in the transcervical subset (7/12 vs. 3/58; p<0.0001). A case-control cohort was constructed to evaluate the impact of these technical variables on sampling efficacy, independent of the influence of uterine position and placental site. In that analysis, suboptimal location and/or orientation of the sampling device remained characteristic of multiple-pass cases. We conclude that further reduction in the frequency of multiple-pass procedures might be achieved by consistent placement of the device tip in the central placental mass. Unlike amniocentesis, where any point of amnion entry will suffice, this technical nuance should be emphasized with CVS to maximize the single-pass success rate.  相似文献   
46.
用结构分析法确定闪石中阳离子的占位已为人们所熟知,本文采用44个碱性闪石的化学分析数据,通过逐步回归分析,从统计学的角度来分析碱性闪石各晶位中阳离子占位率之间的相关性,从而进一步探讨其类质同象的规律,分析表明:碱性问石中作为独立变量的阳离子并非如通常认为的多而杂,如果把碱性闪石类质同象看成一个随机线性向量,则其空间的维数很可能小于10,上述理论计算同时还表明:1.有可能直接用化学分析结果按概率方法对闪石进行定名;2.有可能选择X射线粉末图大于10条特征峰的强度作统计分析来估算闪石中阳离子的占位率。  相似文献   
47.
通过对城市污水处理工艺评价指标的定量化处理,并根据奖优罚劣的原则对初始指标集进行[-1,1]区间线性规范化处理,确定理想最优方案(A^*)和理想最劣方案(A-),以此计算出各待选方案与它们的相关系数(ζ)。采用变异系数法计算各指标权重(ω),并计算各候选方案相对最优方案的灰色关联度,进而确定最佳方案。  相似文献   
48.
Three cases of unusual chromosomal mosaicism are reported for which the cytogenetic data show inconsistent findings between CVS and AC or fetal tissue, and which cannot be explained simply by non-disjunction. For case 1, in CVS the karyotype was 46,XY, whereas lymphocytes and fibroblasts revealed 69,XXY. DNA fingerprinting indicated one paternal and two maternal chromosome sets, the latter most probably due to omission of maternal meiosis II. For case 2, in CVS mos 46,XX/47,XX,+mar de novo was observed. Amniotic fluid cells had the karyotype 46,XX. The origin of the marker chromosome might be explained by at least two events of unknown order (a somatic chromosome/chromatid deletion and non-disjunction of the homologous chromosome). In case 3 (CVS: mos 46,XY/46,XY,19q+ de novo; amniotic fluid cells, lymphocytes, and fibroblasts: 46,XY), the surplus of chromosome material in 19q+ might be explained on the basis of a somatic translocation. The idea of a chimera is less convincing, as the mosaic finding is restricted to one tissue. Furthermore, there was no hint of a vanishing twin. Hitherto, no case of structural chromosome mosaicism in CVS has been reconfirmed in fetal tissues.  相似文献   
49.
A multiple pregnancy of high rank may occur in a couple at risk for a Mendelian disorder. Prenatal diagnosis is hampered by the difficulty of (1) obtaining chorionic villi from each zygote arid (2) unequivocally relating each sample to the corresponding embryo. The calculation of the genetic risk according to the number of zygotes led us to propose a diagnostic strategy based on embryo reduction, a technique initially designed to improve the perinatal outcome of multiple pregnancies with normal embryos. We report a case in which this approach allowed rational use of first-trimester chorionic villus sampling in a quintuplet pregnancy at risk for non-ketotic hyperglycinaemia, resulting in the selective birth of unaffected twins.  相似文献   
50.
We report the first prenatal diagnosis of an affected fetus with Chediak-Higashi syndrome (CHS). Diagnosis was accomplished via fetal blood sampling at 17 menstrual weeks and was confirmed after birth. Retrospective measurement of the largest acid phosphatase-positive lysosomes in cultured amniotic fluid cells and chorionic villus cells showed that in CHS these lysosomes are significantly larger than those in normal cells. This method may be used for prenatal diagnosis of CHS by amniocentesis and chorionic villus sampling (CVS).  相似文献   
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