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排序方式: 共有498条查询结果,搜索用时 31 毫秒
71.
利用卫星观测的气溶胶光学厚度资料和模式模拟数据,与地面颗粒物观测资料结合,探讨近地面颗粒物质量浓度的估算方法。具体包括:利用区域气侯模式RAMS(Regional Atmospheric Modeling System)模拟的边界层高度对气溶胶光学厚度进行垂直订正,获得近地面颗粒物消光系数;利用模式模拟的相对湿度和颗粒物吸湿增长经验模型对消光系数进行湿度订正,获得近地面颗粒物干消光系数;并基于干消光系数与颗粒物质量浓度地面站点资料建立的统计关系估算获得每个像元的颗粒物质量浓度。利用地面站点观测的颗粒物浓度资料验证表明,基于卫星资料可以获得近地面颗粒物质量浓度,而且细颗粒物质量浓度具有更好的估算精度。 相似文献
72.
Suspended particulate matter (SPM) and colloidal matter (COM) in annual dry and wet deposition samples in urban Guangzhou were for the first time collected, and their trace metals were investigated by using inductively coupled plasma mass spectrometry (ICP-MS). The deposition flux of SPM and of metal elements varied largely among the investigated seasons, and reached the maximum in spring. The correlation analysis indicated that significant correlations existed among some of the metal elements in the deposition samples. The enrichment factors (EF) of metals in COM in the deposition ranging from 79.66 to 130,000 were much higher than those of SPM ranging from 1.65 to 286.48, indicating the important role of COM. The factor analysis showed that emissions from street dust, non-ferrous metal production, and heavy fuel oil were major sources of the trace metals. Positive matrix factorization (PMF) model was used to quantitatively estimate anthropogenic source. 相似文献
73.
依托中国“大洋一号”第20和第21调查航次,分析测定了东、西赤道太平洋4个站位的颗粒态生物硅浓度及其粒级结构。结果显示赤道太平洋采样站各层位颗粒态生物硅(PBSi)总浓度分布范围为5~65 nmol/dm3,东赤道太平洋的调查站位颗粒态生物硅的总浓度平均值达46 nmol/dm3,是西赤道太平洋的近3倍。PBSi的粒径结果显示在东赤道太平洋调查站位0.8~20 μm粒径颗粒是PBSi的主要来源,其平均贡献率高达64%;而在西赤道太平洋2种粒径的生物硅贡献率相当。营养盐分布对PBSi的浓度及粒径分布有显著的影响,并在一定程度上控制了“硅质泵”的组成结构,是控制大洋生物泵运转的重要因素。 相似文献
74.
Theodore D. Kanellopoulos Michael O. Angelidis Dimitrios Georgopoulos Aristomenis P. Karageorgis 《Environmental Geology》2009,57(8):1729-1738
Evros River is the most important river flowing into the North Aegean Sea (eastern Mediterranean) in terms of freshwater discharge,
and the second largest one of Eastern Europe after the Danube River. Salinity and temperature measurements, together with
suspended particulate matter concentrations were obtained in various depths at 14 stations in the adjacent Alexandroupolis
Gulf during four seasons (June 1998, September 1998, February 1999 and March 2000) in order to investigate the particle dynamics
and distributions in the northern Aegean Sea. Analysis of the collected data, together with particle observations under the
scanning electron microscope and study of satellite images showed that, under certain circumstances driven by the hydrological
and wind regime of the area, the Evros River particulate matter, with the associated pollutants, can be transferred far away
from the estuary and implicitly comprise a hazardous factor for the environmental status of the northern Aegean Sea. This
fact, combined with the future construction of the Burgas-Alexandroupolis pipeline, may cause a negative impact on the studied
natural ecosystem. 相似文献
75.
Abstract Uptake rates of ammonium (NH4 + ), nitrate (NO3 ? ), and urea by three subgroups of phytoplankton (< 200, < 20, < 2 μm) off Westland, were measured using 15 N tracer techniques in midwinter 1988, after a recent upwelling. For all size fractions at surface irradiance (I100), nitrogen (N) was taken up primarily as NO3 ?. This accounted for 67–85% of total N uptake (SρN), whereas at 40 and 7% of surface irradiance, the regenerated N (NH4 + ) and urea) made up 31–72% of SρN. Depth profile experiments for all three size components showed that uptake of NO3 ? was most light‐sensitive, followed by that of NH4 + and urea. The irradiance and nutrient availability plot indicated that light was substantially more important than the nutrient concentrations in controlling the assimilation of N by microplankton (20–200 μm). Nano‐ (2–20 μm) and picoplankton (< 2 μm) however, were not as sensitive to either light or nutrient concentrations. High winds and the resulting deep mixing, combined with offshore and alongshore advection in the midwinter, were suggested to be the major cause of the low biomass and N productivity. 相似文献
76.
黄河包头段常见离子对重金属在沉积物上吸附影响机制研究 总被引:6,自引:3,他引:3
常见阴阳离子对重金属在黄河包头段相对清洁河段表层沉积物中的吸附影响研究结果表明,不同的环境离子浓度范围内,起主导作用的影响机制不同,黄河包头段水环境中Na 、Mg2 和Ca2 对Zn2 的吸附影响较大,K 对Cu2 、Pb2 、Zn2 和Cd2 吸附影响均较大,Cl-、SO2-4对Cu2 、Pb2 、Zn2 和Cd2 的吸附影响均较小,而HCO-3;对Pb2 的影响较小,对Cu2 、Zn2 、Cd2 的吸附影响较大. 相似文献
77.
P. Pato M. Otero M. Válega C.B. Lopes M.E. Pereira A.C. Duarte 《Marine pollution bulletin》2010,60(10):1658-1666
After having estimated the patterns of flow to the ocean and found some seasonal and tidal differences, mainly with regard to the relative importance of dissolved and particulate fractions, mercury partitioning at the interface between a contaminated lagoon and the Atlantic Ocean was investigated during four tidal cycles in contrasting season and tidal regimes. Mercury was found to be located predominantely in the particulate fraction throughout the year, contributing to its retention within the system. Seasonal conditions, variations in marine and fluvial signals and processes affecting bed sediment resuspension influenced the character and concentration of suspended particulate matter in the water column. Variation in the nature, levels and partitioning of organic carbon in the particulate fraction affected levels of particulate mercury as well as mercury partitioning. These results highlight the dominant role of suspended particulate matter in the distribution of anthropogenic mercury and reinforce the importance of competitive behavior related to organic carbon in mercury scavenging. 相似文献
78.
塔克拉玛干沙漠腹地沙尘暴过程大气颗粒物浓度及影响因素分析 总被引:1,自引:0,他引:1
利用Grimm1.108、Thermo RP 1400a、TSP以及CAWS-600等仪器,对2008年4月17日至23日发生在塔克拉玛干沙漠腹地的1次强沙尘暴过程的颗粒物质量浓度进行连续观测,结合天气资料分析得出:①Grimm1.108颗粒物分析仪监测结果表明,日平均浓度出现两个峰值区,主峰值出现在20日,次峰值出现在18日,而小时平均浓度高值区主要集中4月19日至20日,21日中午存在1个峰值区,其他时段浓度相对较低。②强沙尘暴发生时的分钟观测数据表明,随着风速的逐渐增强,沙尘暴强度逐渐增强,不同粒径颗粒物浓度达到最大值,>0.23 μm颗粒物总浓度为39 496.5 μg·m-3,>20.0 μm颗粒物总浓度为5 390.7 μg·m-3,随后浓度逐渐下降。③PM10和TSP的浓度变化同样反映沙尘天气的过程和强度,沙尘暴前期大气中颗粒物浓度远低于强沙尘暴期间,随沙尘天气减弱,颗粒物浓度明显下降。④沙尘天气过程中大气颗粒物浓度变化具有以下规律:晴天<浮尘天气<浮尘、扬沙天气<沙尘暴天气。风速大小直接影响大气中颗粒物浓度,风速越大颗粒物浓度越高。气温、相对湿度和气压是影响沙尘暴强度的重要因素,也间接影响大气中颗粒物浓度的变化。 相似文献
79.
The fluvial flux of particulate organic matter from the UK: the emission factor of soil erosion 总被引:1,自引:0,他引:1 下载免费PDF全文
Soil erosion has been identified as a potential global carbon sink since eroded organic matter is replaced at source and eroded material is readily buried. However, this argument has relied on poor estimates of the total fate of in‐transit particulates and could erroneously imply soil erosion could be encouraged to generate carbon stores. These previous estimates have not considered that organic matter can also be released to the atmosphere as a range of greenhouse gases, not only carbon dioxide (CO2), but also the more powerful greenhouse gases methane (CH4) and nitrous oxide (N2O). As soil carbon lost by erosion is only replaced by uptake of CO2, this could represent a considerable imbalance in greenhouse gas warming potential, even if it is not significant in terms of overall carbon flux. This work therefore considers the flux of particulate organic matter through UK rivers with respect to both carbon fluxes and greenhouse gas emissions. The results show that, although emissions to the atmosphere are dominated by CO2, there are also considerable fluxes of CH4 and N2O. The results suggest that soil erosion is a net source of greenhouse gases with median emission factors of 5.5, 4.4 and 0.3 tonnes CO2eq/yr for one tonne of fluvial carbon, gross carbon erosion and gross soil erosion, respectively. This study concludes that gross soil erosion would therefore only be a net sink of both carbon and greenhouse gases if all the following criteria are met: the gross soil erosion rate were very low (<91 tonnes/km2/yr); the eroded carbon were completely replaced by new soil organic matter; and if less than half of the gross erosion made it into the stream network. By establishing the emission factor for soil erosion, it becomes possible to properly account for the benefits of good soil management in minimizing losses of greenhouse gases to the atmosphere as a by‐product of soil erosion. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
80.