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41.
Temperature data at different layers of the past 45 years were studied and we found adiploe mode in the thermocline layer (DMT): anomalously cold sea temperature off the coast of Sumatra and warm sea temperature in the western Indian Ocean. First, we analyzed the temperature and the temperature anomaly (TA) along the equatorial Indian Ocean in different layers. This shows that stronger cold and warm TA signals appeared at subsurface than at the surface in the tropical Indian O-cean. This result shows that there may be a strong dipole mode pattern in the subsurface tropical Indian Ocean. Secondly we used Empirical Orthogonal Functions (EOF) to analyze the TA at thermocline layer. The first EOF pattern was a dipole mode pattern. Finally we analyzed the correlations between DMT and surface tropical dipole mode (SDM), DMT and Nino 3 SSTA, etc. and these correlations are strong.  相似文献   
42.
茎柔鱼(Dosidicus gigas)是我国远洋渔业的重要捕捞对象。当前针对茎柔鱼渔场分布及其与环境关系的研究多集中于秘鲁海域,针对赤道海域茎柔鱼特定种群小型群体资源分布及其渔场环境特征研究较少。根据2019年12月至2020年2月茎柔鱼生物学数据,2019年12月至2020年4月生产和环境数据,运用胴长-体重关系拟合、地统计插值、广义可加模型(GAM)探究其资源分布及渔场环境状况。结果表明:东太平洋赤道海域茎柔鱼胴长范围为136~407 mm,体重范围为117~1557 g;2019年12月至2020年4月各月渔获量呈先增加后减小趋势,2月渔获量最高;CPUE曲线除2月增加外,总体呈下降趋势;渔场集中分布于0°~3°S、105°W~114°W海域,不同月份渔场重心经向变化明显;渔场最适SST范围是24.5~25.5 °C,最适Chl-a范围是0.16~0.20 mg/m3,月份是影响茎柔鱼CPUE的主要因子。研究表明:该海域茎柔鱼渔获主要为小型群体;小型群体生长发育期(2–3月)对渔场分布有重要影响,生长发育期前茎柔鱼集群度高,生长发育期后逐渐分散活动;单一影响因子与茎柔鱼CPUE相关性不显著,综合考虑其他环境因素及其交互影响是今后的研究方向。  相似文献   
43.
中国第22次南极科学考察(2005年11月至2006年3月)期间,测定了南极普里兹湾海域5个站位的从表层至150 m水深的不同层位水样中溶解态和颗粒态234Th,238U的放射性比活度以及颗粒有机碳.利用234Th/238U在上层水体中的不平衡,计算了南极普里兹湾上层水体中234Th的平均停留时间和输出通量.结果显示,随着纬度的增加,上层水体中颗粒态和溶解态234Th的平均停留时间总体趋向减小,并在中纬度站位出现了最低值,分别为1~8和29~48 d,而颗粒态和溶解态234Th的输出通量则在中纬度站位出现了最大值,分别为21~38和26~39 dpm/(m3·d).运用箱型清除模式,利用两种不同的方法估算了各水柱中从真光层底部输出的POC通量,平均值分别达到104.7 mmol/(m2·d)(E法)和120.6 mmol/(m2·d)(B法),表明南极普里兹湾夏季存在很高的新生产力,它将会对该海域碳的生物泵过程产生重要作用.  相似文献   
44.
东亚冬夏季风对热带印度洋秋季海温异常的响应   总被引:5,自引:0,他引:5  
利用多年的Reynolds月平均海表温度资料和NCEP/NCAR全球大气再分析资料,分析了热带印度洋秋季海表温度距平(SSTA)与后期东亚冬夏季风强度变化的关系。结果表明,热带印度洋秋季SSTA的主要模态是全区一致(USB)型和偶极子(IOD)型,USB型模态主要代表热带印度洋秋季SSTA的长期变化趋势,而IOD型模态主要反映热带印度洋秋季SSTA的年际变化。热带印度洋秋季海温气候变率中既存在着明显的ENSO信号,也有独立于ENSO的变率特征,独立于ENSO的热带印度洋秋季SSTA变化的主要模态仍是USB型和IOD型。前期秋季USB模态与东亚冬季风及东亚副热带夏季风之间为负相关关系;与前期正(负)IOD模态相对应,南海夏季风强度偏弱(强),而东亚副热带夏季风强度偏强(弱)。USB型和IOD型模态对后期东亚冬、夏季风强度变化的影响是独立于ENSO的,但ENSO起到了调节二者相关显著程度的作用。  相似文献   
45.
On the basis of maps of sea level anomalies data set from October 1992 to January 2004, pronounced low frequency variations with periods of about 500 d are detected in the area near 20°N from 160°W to 130°E. A linear two-layer model is employed to explain the mechanism. It is found that the first-mode long baroclinic Rossby waves at 20°N in the northwest Pacific propagate westward in the form of free waves at a speed of about 10.3 cm/s. This confirms that the observed low frequency variabilities appear as baroclinic Rossby waves. It further shows that these low frequency variabilities around 20°N in the northwest Pacific can potentially be predicted with a lead up to 900 d.  相似文献   
46.
热带印度洋偶极子发生和演变机制的数值研究   总被引:5,自引:0,他引:5  
对中国科学院大气物理研究所(IAP)大气科学和地球流体力学数值模拟国家重点实验室(LASG)发展的第三代海洋模式(L30T63 OGCM)进行了改进。分析了该模式1959年1月—1998年12月的40a积分结果,以此研究热带印度洋偶极子发生、发展和消亡的物理机制。对数值模拟结果的分析表明,赤道印度洋表面异常东风引起的异常环流结构是偶极子发生、发展的主要动力学原因,其表面异常东风转换为异常西风所引起的异常环流结构调整是偶极子消亡的主要动力学原因;海气界面热通量异常的交换对热带印度洋海表温度距平偶极子模态的形成和演变起着重要的作用;垂直输送作用是热带印度洋次表层海温偶极子模态发生和演变的主要物理机制。  相似文献   
47.
48.
The absorption of anthropogenic CO2 and atmospheric deposition of acidity can both contribute to the acidification of the global ocean. Rainfall pH measurements and chemical compositions monitored on the island of Bermuda since 1980, and a long-term seawater CO2 time-series (1983–2005) in the subtropical North Atlantic Ocean near Bermuda were used to evaluate the influence of acidic deposition on the acidification of oligotrophic waters of the North Atlantic Ocean and coastal waters of the coral reef ecosystem of Bermuda. Since the early 1980's, the average annual wet deposition of acidity at Bermuda was 15 ± 14 mmol m− 2 year− 1, while surface seawater pH decreased by 0.0017 ± 0.0001 pH units each year. The gradual acidification of subtropical gyre waters was primarily due to uptake of anthropogenic CO2. We estimate that direct atmospheric acid deposition contributed 2% to the acidification of surface waters in the subtropical North Atlantic Ocean, although this value likely represents an upper limit. Acidifying deposition had negligible influence on seawater CO2 chemistry of the Bermuda coral reef, with no evident impact on hard coral calcification.  相似文献   
49.
Sediment samples ranging from 0.05 to 278 m below sea floor (mbsf) at a Northwest Pacific deep-water (5564 mbsl) site (ODP Leg 191, Site 1179) were analyzed for phospholipid fatty acids (PLFAs). Total PLFA concentrations decreased by a factor of three over the first meter of sediment and then decreased at a slower rate to approximately 30 mbsf. The sharp decrease over the first meter corresponds to the depth of nitrate and Mn(IV) reduction as indicated by pore water chemistry. PLFA-based cell numbers at site 1179 had a similar depth profile as that for Acridine orange direct cell counts previously made on ODP site 1149 sediments which have a similar water depth and lithology. The mole percentage of straight chain saturated PLFAs increases with depth, with a large shift between the 0.95 and 3.95 mbsf samples. PLFA stable carbon isotope ratios were determined for sediments from 0.05 to 4.53 mbsf and showed a general trend toward more depleted δ13C values with depth. Both of these observations may indicate a shift in the bacterial community with depth across the different redox zones inferred from pore water chemistry data. The PLFA 10me16:0, which has been attributed to the bacterial genera Desulfobacter in many marine sediments, showed the greatest isotopic depletion, decreasing from − 20 to − 35‰ over the first meter of sediment. Pore water chemistry suggested that sulfate reduction was absent or minimal over this same sediment interval. However, 10me16:0 has been shown to be produced by recently discovered anaerobic ammonium oxidizing (anammox) bacteria which are known chemoautotrophs. The increasing depletion in δ13C of 10me16:0 with the unusually lower concentration of ammonium and linear decrease of nitrate concentration is consistent with a scenario of anammox bacteria mediating the oxidation of ammonium via nitrite, an intermediate of nitrate reduction.  相似文献   
50.
Dissolved and particulate samples were collected to study the distribution of thorium isotopes (234Th, 232Th and 230Th) in the water column of the Indian sector of the Southern Ocean (from 42°S to 47°S and from 60°E to 66°E, north of the Polar Front) during Austral summer 1999. Vertical profiles of excess 230Th (230Thxs) increases linearly with depth in surface water (0–100 m) and a model was applied to estimate a residence time relative to the thorium scavenging (τscav). Low τscav in the Polar Front Zone (PFZ) are found, compared to those estimated in the Subtropical Front Zone (STZ). Changes in particle composition between the PFZ and STZ could influence the 230Thxs scavenging efficiency and explain this difference. An innovative coupling between 234Th and 230Thxs was then used to simultaneously constrain the settling velocities of small (0.6–60 μm) and large (above 60 μm) particles. Although the different hydrological and biogeochemical regimes visited during the ANTARES IV cruise did not explain the spatial variation of sinking velocity estimates, our results indicate that less particles may reach the seafloor north (60 ± 2 m d− 1, station 8) than south of the Agulhas Return Current (119 ± 23 and 130 ± 5 m d− 1 at stations 3 and 7, respectively). This information is essential for understanding particle transport and by extension, carbon export. In the deep water column, the 230Thxs concentrations did not increase linearly with depth, probably due to lateral transport of North Atlantic Deep Water (NADW) from the Atlantic to the Indian sector, which renews the deep waters and decreases the 230Thxs concentrations. A specific 230Thxs transport model is applied in the deep water column and allows us to assess a “travel time” of NADW ranging from 2 to 15 years.  相似文献   
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