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   1127篇
  免费   167篇
  国内免费   214篇
测绘学   2篇
大气科学   225篇
地球物理   253篇
地质学   607篇
海洋学   228篇
天文学   90篇
综合类   27篇
自然地理   76篇
  2024年   4篇
  2023年   19篇
  2022年   24篇
  2021年   34篇
  2020年   41篇
  2019年   25篇
  2018年   27篇
  2017年   35篇
  2016年   32篇
  2015年   33篇
  2014年   38篇
  2013年   41篇
  2012年   36篇
  2011年   49篇
  2010年   44篇
  2009年   62篇
  2008年   80篇
  2007年   71篇
  2006年   83篇
  2005年   65篇
  2004年   79篇
  2003年   58篇
  2002年   55篇
  2001年   38篇
  2000年   71篇
  1999年   59篇
  1998年   44篇
  1997年   43篇
  1996年   37篇
  1995年   24篇
  1994年   29篇
  1993年   27篇
  1992年   17篇
  1991年   4篇
  1990年   21篇
  1989年   9篇
  1988年   11篇
  1987年   9篇
  1986年   5篇
  1985年   10篇
  1984年   8篇
  1983年   1篇
  1981年   1篇
  1980年   3篇
  1978年   2篇
排序方式: 共有1508条查询结果,搜索用时 15 毫秒
121.
Severe chemical ozone loss has been detected in the Arctic in the winter and spring of 1995–96 by a variety of methods. Extreme reductions in column ozone due to halogen catalysed chemistry were derived from measurements of the Halogen Occultation Experiment (HALOE) on board the Upper Atmosphere Research Satellite in the Arctic vortex. Here, we discuss further aspects of the HALOE observations in the Arctic over this period. Potential problems, both in the data themselves and in the methodology of the data analysis are considered and the reason for the differences between the Arctic ozone losses deduced from HALOE data version 17 and 18 is analysed. Moreover, it is shown that HALOE measurements in the Arctic in winter and spring 1995–96 compare well with observations by other ground-based and satellite instruments.  相似文献   
122.
喀斯特区域的水化学不稳定性——以黔中地区为例   总被引:2,自引:0,他引:2       下载免费PDF全文
黔中地区是岩溶作用发育的喀斯特区域.1993年秋和1994年春末采自该地区不同类型水样的水化学分析表明:碳酸盐岩裂隙泉水呈中偏碱性,为[C]Ca-Ⅱ型;秋季离子总量、HCO3-及Ca2+浓度大于春季.裂隙泉水流经地表一定距离后,HCO3-降低,pH及SO42-、Cl-、K+、Na+明显增高.黄果树的天星桥、水帘洞及落水潭三个部位河水的SO42-、Na+以及Fe3+、NO3-等浓度的季节性变化也更加明显.春季因瀑布暴气,CO2的逸出,钙华生成更强烈一些.红枫湖作为喀斯特区域地表水的汇集地,HCO3-与SO42-的当量比值仅2.1~2.4;Ca2+与Mg2+比值上升为2.4~4.2,Cl-浓度较碳酸盐岩裂隙泉水增高1倍;Na+浓度增高一个数量级.说明流域内地表土层溶蚀及人为污染影响的增强.土层孔隙水属强矿化水,而湖水呈现过渡特征.碳酸盐沉淀作用、硫酸盐矿化作用及固氮氨化作用,导致水质组成的显着差异.  相似文献   
123.
Water samples collected in the Negro River drainage basin (Patagonia, Argentina) during two different field trips—the first in May 1972 and the second in January 1973—were analysed for the major dissolved inorganic constituents. Q-mode factor analyses demonstrate that two factors account for over 98 per cent of the variance in both sample suites. They represent: a) the direct influence of solution of evaporites and associated carbonate rocks in an arid environment-type; b) the influence of the weathering products of metamorphic, igneous rocks, and varied non-calcareous sediments. R-mode factor analyses of the two sets of data suggest that although the main mechanisms controlling water chemistry were essentially the same, the principal sources of dissolved solids differed significantly in each separate occasion. Further, the major mechanisms controlling its water chemistry are within a wide spectrum of the so-called ‘rock dominance’.  相似文献   
124.
Atmospheric mercury concentrations were measured during a nautical expedition on the Atlantic Ocean between Hamburg (54°N, 10°E) and Santo Domingo (20°N, 67°W). In addition, samples were taken during flights on a commerical aircraft in the upper and middle troposphere between 60°N and 55°S, mostly over the Pacific Ocean. The data obtained in the lower troposphere over the Northern Atlantic show considerable variation in the Hg concentrations, with values ranging between 1 and 11 ng/m3; the average concentration was found to be 2.8 ng/m3. The upper tropospheric data show an interhemispheric difference with average values of 1.45 ng/m3 and 1.08 ng/m3 in the Northern and Southern Hemisphere, respectively. This suggests that mercury production occurs predominantly over the continents both by natural and anthropogenic processes. The mercury content in aerosols was found to be 0.3 ng/m3, or one-tenth of the atmospheric concentration. The data indicate a mean residence time of mercury in the atmosphere of a few months to one year.  相似文献   
125.
Rainwater samples (wet-only; event samples) collected in Niigata in late autumn 1996 and springtime 1997 were used to assess the effectiveness of thymol as a biocide in Japanese rainwater. Upon collection each rainwater sample was divided into sub-samples, with thymol added to one sub-sample. Sub-samples with and without thymol were shipped to CSIRO, Australia, for chemical analysis. Comparison of analytical results for each pair of sub-samples proved the effectiveness of thymol in preventing biological action in this region where effects of rainwater microflaura and fauna on rainwater composition have not before been studied. Sub-samples without thymol exhibited lowered electrical conductivity, loss of the cations H+ and NH 4 - , and loss of the anions HCOO-, CH3COO-, C2O 4 2- , CH3SO 3 - and PO 4 3- . Nitrate showed no change in all but one of the samples, indicating that ammonia was the preferred source of nitrogen for the biological processes that consumed the rainwater organic acids and phosphate. These results suggest that thymol is a suitable rainwater biocide for use under Japanese conditions.  相似文献   
126.
A box model was constructed to investigate connections between the particulate MSA to non-sea-salt sulfate ratio, R, and DMS chemistry in a clean marine boundary layer. The simulations demonstrated that R varies widely with particle size, which must be taken into account when interpreting field measurements or comparing them with each other. In addition to DMS gas-phase chemistry, R in the submicron size range was shown to be sensitive to the factors dictating sulfate production via cloud processing, to the removal of SO2 from the boundary layer by dry deposition and sea-salt oxidation, to the entrainment of SO2 from the free troposphere, to the relative concentration of sub- and supermicron particles, and to meteorology. Three potential explanations for the increase of R toward high-latitudes during the summer were found: larger MSA yields from DMS oxidation at high latitudes, larger DMSO yields from DMS oxidation followed by the conversion of DMSO to MSA at high latitudes, or lower ambient H2O2 concentrations at high latitudes leading to less efficient sulfate production in clouds. Possible reasons for the large seasonal amplitude of R at mid and high latitudes include seasonal changes in the partitioning of DMS oxidation to the OH and NO3 initiated pathways, seasonal changes in the concentration of species participating the DMS-OH reaction pathway, or the existence of a SO2 source other than DMS oxidation in the marine boundary layer. Even small anthropogenic perturbations were shown to have a potential to alter the MSA to non-sea-salt sulfate ratio.  相似文献   
127.
胶东半岛位于欧亚板块与太平洋板块边缘内侧 ,是地壳长期稳定缓慢隆起地段 ,区内地质构造发育 ,大部分温泉出露在背斜核部 ,NE、NNE向与NW、NNW向断裂交汇处。地热系统属中低温深循环对流型 ,略为偏高的大地热流是其主要热源 ,地表水是地下热水的补给水源 ,地下水通过发育在花岗岩和变质岩中的断层或断裂破碎带 ,下渗和深循环对流 ,在径流过程中不断吸取围岩热量成为热水 ,沿断裂上升过程中 ,与地下浅部裂隙水混合而成为化学成分各异 ,温度高低不等的温泉水  相似文献   
128.
广东汕头湾表层沉积物重金属含量分布及风险评价   总被引:1,自引:0,他引:1       下载免费PDF全文
汕头湾地处汕头东部,是珠三角经济区和海峡西岸经济区重要的海上交通枢纽。因受周边城镇、养殖区排污等影响,汕头湾的海洋环境已受污染,生态健康问题不容忽视。沉积物中重金属是反映区域环境质量的重要因子,本研究通过测定汕头湾海域29个表层沉积物样品中重金属Zn、Cu、Cr、Cd、Pb、Hg、As含量,分析了各元素的平面分布特征,并运用主成分分析法(PCA)、地累积指数法和潜在生态风险指数法对该区域沉积物中重金属的来源及潜在生态风险进行了探讨。结果表明:汕头湾海域表层沉积物的金属含量变化范围为CZn(15. 3~280. 4 mg/kg)、CCu(2. 0~84. 6mg/kg)、CCr(3. 0~130. 8 mg/kg)、CCd(0. 05~1. 07 mg/kg)、CPb(12. 97~39. 31 mg/kg)、CHg(0. 008~0. 171 mg/kg)、CAs(1. 60~16. 50 mg/kg),榕江入海口处为重金属元素的高值区,在拦沙堤的两侧,元素Zn、Cu、Cr、Cd的含量差别较大。相关性分析和主成分分析结果显示,重金属具有相同污染来源,工业废水和城市排污等人类活动输入是主要途径,其分布特征受有机碳、硫化物及细粒级组分等环境因子的影响。地累积指数法和潜在生态风险指数法的结果表明,在榕江入海口附近区域,重金属表现出强的生态风险,而拦沙堤东侧海域为轻微生态风险,Hg、Cu、Cd是主要污染元素。  相似文献   
129.
Otoliths are calcified structures in the head of fish that record environmental information about fish's life history. Gathering the elemental information from the core of an otolith corresponding to the juvenile period of fish's life is critical to discriminate the adult fish to their natal habitats reliably. A high resolution micromill has been used to isolate the otolith core from a whole otolith for elemental analysis. The effects of micromilling procedures (e.g., sectioning, embedding and drilling) on contamination to otolith trace element levels were examined using paired blackfin tuna (Thunnus atlanticus) otoliths. Otoliths were decontaminated by dilute hydrogen peroxide and nitric acid throughout to remove surface contamination. A preconcentration procedure was used to determine the trace elements from the small core material by ICP-MS. It was found that micromilling procedures introduce significant contamination to otoliths, especially for Al, Cu, Pb and Zn. The sectioning procedure caused significant contamination for Co and Cu, while the embedding procedure resulted in contamination for nearly all trace elements (Al, Cd, Co, Cu, Ga, Mn, Ni, Pb, V and Zn). The combined sectioning, embedding and drilling procedure also resulted in contamination for most trace elements. Despite the contamination across all procedural steps, the decontamination procedure effectively removed the surface contamination with the exception of Pb and Zn. Bias (e.g., residual contamination) on Pb was small in comparison to overall concentration of Pb expected to occur in fish otoliths, therefore, its effect may be minor in discriminating individuals. Bias on Zn was larger that could limit its application in discriminating individuals.  相似文献   
130.
Summer stream water quality was monitored before and following the logging of 50% of the boreal forest within three small watersheds (<50 ha) nested in the ‘Ruisseau des Eaux‐Volées’ Experimental Watershed, Montmorency Forest (Québec, Canada). Logging was conducted in winter, on snow cover according to recommended best management practices (BMPs) to minimize soil disturbance and protect advance growth. A 20‐m forest buffer was maintained along perennial streams. In watershed 7·2, cut‐blocks were located near the stream network and logging was partially allowed within the riparian buffer zone. In watersheds 7·5 and 7·7, logging occurred farther away from the stream network. Observations were also made for watershed 7·3 that collected the runoff from watersheds 7·2 and 7·5, and watershed 7·6, the uproad portion of watershed 7·7. The control watershed 0·2 was contiguous to the impacted watersheds and remained undisturbed. Following clearcutting, changes in summer daily maximum and minimum stream temperatures remained within ± 1 °C while changes in diurnal variation did not decrease by more than 0·5 °C. Concentrations of NO3? greatly increased by up to 6000% and concentrations of K+ increased by up to 300% during the second summer after logging. Smaller increases were observed for Fetotal (up to 71%), specific conductance (up to 26%), and Mg2+ (up to 19%). Post‐logging pH decreased slightly by no more than 7% while PO43? concentration remained relatively constant. Suspended sediment concentrations appeared to increase during post‐logging, but there was not enough pre‐logging data to statistically confirm this result. Logging of moderate intensity and respecting established BMPs may account for the limited changes of water quality parameters and the low exceedances of the criteria for the protection of aquatic life. The proximity of the cutover to the stream network and logging within the riparian zone did not appear to affect water quality. Copyright © 2008 John Wiley & Sons, Ltd.  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