首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   665篇
  免费   12篇
  国内免费   8篇
安全科学   24篇
废物处理   48篇
环保管理   31篇
综合类   126篇
基础理论   149篇
环境理论   1篇
污染及防治   192篇
评价与监测   82篇
社会与环境   25篇
灾害及防治   7篇
  2023年   12篇
  2022年   24篇
  2021年   21篇
  2020年   12篇
  2019年   11篇
  2018年   34篇
  2017年   27篇
  2016年   41篇
  2015年   22篇
  2014年   44篇
  2013年   75篇
  2012年   42篇
  2011年   45篇
  2010年   37篇
  2009年   23篇
  2008年   16篇
  2007年   19篇
  2006年   20篇
  2005年   10篇
  2004年   15篇
  2003年   12篇
  2002年   23篇
  2001年   8篇
  2000年   9篇
  1999年   5篇
  1997年   4篇
  1995年   3篇
  1994年   2篇
  1993年   5篇
  1986年   2篇
  1982年   2篇
  1980年   2篇
  1972年   1篇
  1971年   2篇
  1970年   6篇
  1969年   2篇
  1968年   1篇
  1967年   4篇
  1966年   3篇
  1965年   2篇
  1964年   1篇
  1961年   1篇
  1960年   4篇
  1959年   4篇
  1958年   10篇
  1957年   4篇
  1956年   3篇
  1955年   1篇
  1931年   1篇
  1930年   2篇
排序方式: 共有685条查询结果,搜索用时 15 毫秒
271.
272.
273.
结合桐柏县的实例,对县域生态功能区划分的原则和方法进行初步探讨。综合利用3S技术对县域生态敏感性和生态服务功能重要性的分析和评价,提出桐柏县生态服务功能区划的初步方案。将桐柏县划分为生态支持区,产品供给区,生态调节区。简要分析了各功能区在桐柏县经济可持续发展中的地位和作用,指出各区协调发展的方向和途征。  相似文献   
274.
甾烷作为溢油指示物的模糊聚类分析研究   总被引:6,自引:0,他引:6  
用模糊聚类分析对溢油指示物甾烷进行了研究,为消除进样误差的影响,以标准化相对峰高为基本数据,推算出了油种及其甾烷的动态模糊聚类分析图。结果表明,油种的动态模糊聚类分析图可以显示油种间的疏近程度;甾烷的动态模糊聚类分析图可以表征溢油指示物各甾烷的贡献率,15个甾烷是模糊聚类分析的主要因子,属较理想的溢油指示物。  相似文献   
275.
Adsorption kinetics of methyl violet onto perlite   总被引:11,自引:0,他引:11  
Doğan M  Alkan M 《Chemosphere》2003,50(4):517-528
This study examines adsorption kinetics and activation parameters of methyl violet on perlite. The effect of process parameters like contact time, concentration of dye, temperature and pH on the extent of methyl violet adsorption from solution has been investigated. Results of the kinetic studies show that the adsorption reaction is first order with respect to dye solution concentration with activation energy of 13.2 kJ mol(-1). This low activation energy value indicates that the adsorption reaction is diffusion controlled. The activation parameters using Arrhenius and Eyring equations have been calculated. Adsorption increases with increase of variables such as contact time, initial dye concentration, temperature and pH.  相似文献   
276.
In the period from 1980 to 1984 organic phosphorus, nutrients, primary production rates (14C), chlorophyll a (chl a) standing crops, and basic oceanographic parameters were measured during 23 cruises at six stations in the open waters of the northern Adriatic Sea. These waters are significantly influenced by polluted Po River discharge. Organic phosphorus was correlated with several parameters which characterize phytoplankton activity and organic matter decomposition processes. In the late winter-spring period, organic phosphorus is produced during phytoplankton blooms. It is hypothesized that microzooplankton grazing is the main factor increasing the organic phosphorus concentrations in summer (up to 1.1 mol 1-1). Fall and winter had much lower values (below 0.3 mol 1-1) due to remineralization processes and an increased water mass exchange between the northern and central Adriatic regions. The direct contribution of organic phosphorus by freshwater discharge was not found to be significant. The higher organic phosphorus concentrations that can occur in low salinity waters are most likely due to their increased capability to support primary production.  相似文献   
277.
The reproductive season of the Adelomelon brasiliana population of Mar del Plata extends from September to April (austral spring and summer), showing synchronisation with water temperature. Adult gonad state is related to shell-free wet mass. Oocytes reach 200 m in diameter before spawning. In autumn, a resting phase begins, when no new oocytes develop and the non-spawned ones undergo reabsorption. Gonadic development begins during the early winter, when new previtellogenic oocytes can be observed through histology. The long reproductive season would increase the ability of the species to recover from harvesting.Communicated by O. Kinne, Oldendorf/Luhe  相似文献   
278.
The relationship between somatic growth and growth of otoliths of sea bass larvae, postlarvae and juveniles under relatively steady temperature conditions was studied. Larvae were incubated at the constant ambient temperature of 13.5°C, whereas postlarvae and juveniles were reared at a comparatively steady temperature ranging from 18.6 to 20.4°C, with a mean of 19.67°C. The patterns of both somatic and otolith growth were found to be similar. Differentiated data on larvae length and otolith diameters indicated three periods of change in their growth rates. Since temperature was kept relatively steady during the experiment, and larvae fed ad libitum, these periods could be attributed with relative certainty to intrinsic changes which occur during stage-specific periods of growth. The third period of change in both growth rates indicates a specific phase of growth during metamorphosis. The changes in growth rates, as well as the raw time series of the growth of both larval lengths and otolith diameters, may be described by higher order polynomials with a high degree of probability levels. A non-linear relationship between body length and otolith diameters was established, indicating positive allometric growth of otoliths. It was also observed that the coefficient of allometric growth changed at the time estimated for the end of metamorphosis. Thus, a non-linear relationship and changes in the coefficients of allometry should be borne in mind when back-calculating somatic growth from the growth of otoliths.  相似文献   
279.
Age, growth and population structure of Modiolus barbatus from Mali Ston Bay, Croatia were determined using modal size (age) classes in length frequency distributions, annual pallial line scars on the inner shell surface, internal annual growth lines in shell sections of the middle nacreous layer and Calcein marked and transplanted mussels. The length frequency distributions indicated that M. barbatus attain a length of ∼40 mm in 5–6 years indicating that a large proportion of the population in Mali Ston Bay is <5 years old. Some mussels of ∼60 mm were predicted to be 14 years old using the Von Bertalanffy growth (VBG) equation. Up to the first 6 pallial line scars were visible in young (<6 years) mussels but in older shells the first scars became obscured by nacre deposition as the mussel increased in length and age. The age of the older shells (>6 years) was determined from the middle nacreous lines in shell section, which formed annually in winter between February and March; the wider dark increments forming during summer (June to September). The oldest mussel, determined from the middle nacreous lines, was >12 years, with the majority of mussels aged between 3 and 6 years of age. The ages of mussels ascertained using the growth lines were not dissimilar to the ages predicted from the length frequency distributions. Age at length curves produced using modal size class data were not different from the data obtained using the pallial scar rings and internal growth lines. Taken together these data suggest that M. barbatus attains a length of 40 and 50 mm within 5 and 8 years, respectively. Eighty one percent of individual M. barbatus injected with a Calcein seawater solution (300 mg Calcein l−1), into their mantle cavity successfully deposited a fluorescent line, which was visible in suitably prepared shell sections under ultra violet light. Incorporation of Calcein into the mussel shells was seasonally variable with the lowest frequency of incorporation in mussels marked in February and recovered in May. Seasonal shell growth was observed with significantly higher growth rates in mussels marked in May and removed in August (ANCOVA, F 3,149 = 23.11, P < 0.001). Mussels (∼18 to 22 mm) marked in May and recovered in August displayed maximal growth rates of >2.5 mm month−1 compared with a mean mussel growth rate of 1.2 ± 0.6 mm month−1. At other times of the year mussel shell growth ranged from immeasurable to 1.48 mm month−1.  相似文献   
280.
本文研究了在自然状况下污水塘的净化作用及其效率,通过对总氮、总磷、COD_(Cr)和BOD_5等在进、出水中的含量与水温进行回归分析,建立了三者之间的相关性方程。同时讨论了水温对污水塘的自净效率的影响。  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号