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71.
对虾养殖生态系中有机碳的初步研究本研究由 总被引:1,自引:0,他引:1
对于围隔养殖对虾生态系中有机碳的变动进行了研究 ,结果表明 :溶解有机碳 (DOC)含量波动在 5 .2 99~ 13.39mg/ L之间 ,平均为 8.5 3mg/ L± 2 .2 5 mg/ L;颗粒有机碳 (POC)含量波动在0 .6 5~ 6 .6 3mg/ L之间 ,平均为 3.2 5 mg/ L± 1.76 mg/ L;总有机碳 (TOC)含量波动在 6 .92~ 2 0 .0 2mg/ L之间 ,平均为 11.78mg/ L± 3.82 mg/ L ;其中 DOC∶ POC∶ TOC为 0 .72∶ 0 .2 8∶ 1。各种有机碳组分的含量明显高于自然海水中各种有机碳的含量 ;各种有机碳组分的含量在养殖期间总体上呈上升的趋势 ;其变化与 DCOD的变化呈显著线性正相关的关系。 相似文献
72.
根据1988年7月调查资料讨论了台湾海峡中北部海域夏季上升流区各种形态磷的分布特征。结果表明,上升流中心区(即海坛岛东侧一带水域)具有低温、高盐、低溶解氧;DIp,TDP,PP,TP较高;DOP较低(0.27);及DIP/DOP比值(约为1)较高的特性。DOP是该海域磷的主要形态(占TP的49.2%),其含量分布及其形态转化与生物活动直接相关,是该海域生物生产力高的体现。 相似文献
73.
分别于1989年,1992年,1991年8月,1991年5月对大辽河口、鸭绿江口、滦河口、东村河口水体中总汞进行了取样和分析,其中又对大辽河口和东村河口进行了溶解态汞的分析。大辽河口和东村河口溶解态汞的含量分别为85~460ng/L和180~500ng/L,平均值分别为210和324ng/L;总汞含量分别为95~550和400~1000ng/L,平均值分别为310和640ng/L。大辽河河流段和河口段溶解态汞和颗粒态汞是主要存在形式。河口溶解态汞和颗粒态汞随氯度变化趋势相似。东村河口溶解态汞约占50%。鸭绿江口和滦河口总汞含量分别为30~2500和3700~6700ng/L,平均值分别为700和5700ng/L。鸭绿江口总汞随氯度变化趋势与随浊度变化趋势一致。而在滦河口总汞含量随两者变化趋势则不同。还讨论了滦河口、东村河口、鸭绿江口和大辽河口汞的污染程度。 相似文献
74.
Ocean Color Satellite Imagery and Shipboard Measurements of Chlorophyll a and Suspended Particulate Matter Distribution in the East China Sea 总被引:1,自引:0,他引:1
Satellite-derived ocean color data of Coastal Zone Color Scanner (CZCS) on board the Nimbus-7 and Ocean Color and Temperature Scanner (OCTS) on board the Advanced Earth Observing Satellite (ADEOS) are jointly used with historical in situ data to examine seasonal and spatial distributions of chlorophyll a (Chl-a) and suspended particulate matter (SPM) concentrations in the East China Sea. Ocean color imagery showed that Chl-a concentrations on the continental shelf were higher than those of the Kuroshio area throughout the year. Satellite-derived Chl-a concentrations are generally in good accordance with historical in situ values during spring through autumn (although no shipboard in situ measurement was conducted at nearshore areas). In contrast, ocean color imagery in winter indicated high Chl-a concentrations (4–10 mg m–3) on the continental shelf where bottom depth was less than 50 m when surface water was turbid (2–72 g m–3 of SPM at surface), while historical in situ values were usually less than 1 mg m–3. This suggests that resuspended bottom sediment due to wind-driven mixing and winter cooling is responsible for the noticeable overestimation of satellite-derived Chl-a concentrations. The algorithm for ocean color needs to be improved urgently for turbid water. 相似文献
75.
Modelling nitrogen and phosphorus cycles and dissolved oxygen in the Zhujiang Estuary Ⅰ. Model development 总被引:1,自引:0,他引:1
wrmcrloxHuman activities related to the population growth and developrnent of industry and rnwhci-pality have led to the incrouing hadings of various POllutants into estudries during the past fewdecades. These increasing edlutant lOadings have caused declined estuallne hedth which can bemereured by a vdriety of indices. In order to obtain solutions to environrnent problerns, re-sources manageTnnt apencies are supporting a holistic approach to envirorirnental management.An effcient strategy t… 相似文献
76.
77.
台湾海峡中北部夏季溶解氧饱和度分布与上升流的关系 总被引:1,自引:1,他引:1
本文据台湾海峡中北部1983年5月至1984年5月、1987年7,8月和1988年5~7月调查资料,讨论了该海域夏季溶解氧饱和度分布特征及其与上升流的关系,结果表明该海区夏季上升流的中心位置经常出现于海坛岛北侧至湄洲岛一带海域,西南季风是该区上升流产生的主要动力因子,该区上升流平均流速为4.4×10~(-3)cm/s。 相似文献
78.
Vertical and seasonal characteristics of biogenic silica (BSi) dissolution in seawater were investigated by multiple dissolution experiments using seawater collected from surface and mesopelagic layers in Suruga Bay during the period 2002–2004. The dissolution rate coefficients calculated based on temporal changes of BSi concentration varied with the season of sample collection. They ranged from 0.023–0.057 day− 1 for surface samples and 0.0018–0.0025 day− 1 for mesopelagic samples for temperatures approaching in situ conditions. Experiments at various temperatures confirmed that BSi dissolution depends on temperature in natural seawater. Dissolution rate coefficient (day− 1) of BSi correlated significantly with temperature (°C), and Q10 was 2.6. Addition of bioavailable organic matter to low-bioactivity seawater enhanced the protease activity and abundance of bacteria, and increased BSi dissolution rate by a factor of 1.4–2.0. There is clear evidence that BSi dissolution is accelerated by bacterial activity and potentially limited by bioavailable organic matter in natural seawater. Dissolution rates and total decreases of BSi concentration were lower during experiments using mesopelagic samples than in those using surface samples. This suggests that dissolution of BSi varies with depth and that BSi in the mesopelagic water is more resistant to the dissolution than that in the surface water. This lower dissolution rate was caused by lower temperature and lower bacterial activity due to less bioavailable organic matter in mesopelagic water. Our results provide a mechanistic understanding of variations in silica cycling within the seasonally and vertically differing marine environment. 相似文献
79.
C.G. Castro M. Nieto-Cid X.A. lvarez-Salgado F.F. Prez 《Deep Sea Research Part I: Oceanographic Research Papers》2006,53(12):1925-1940
The short-time-scale variability of the remineralization patterns in the domain of Eastern North Atlantic Central Waters (ENACW) off the NW Iberian Peninsula is studied based on biogeochemical data (oxygen, nutrient salts, total alkalinity, pH, dissolved organic matter and fluorescence of dissolved humic substances) collected weekly between May 2001 and April 2002. The temporal variability of inorganic variables points to an intensification of remineralization during the summer and autumn, with an increase of nutrients, total inorganic carbon and fluorescence and a decrease of oxygen. During the subsequent winter mixing, there is a biogeochemical reset of the system, with lower nutrients, total inorganic carbon and fluorescence and higher oxygen. In contrast to inorganic variables, the levels of dissolved organic matter in the ENACW seem to respond to short-term events probably associated with fast sinking particles, where solubilisation of organic matter prevails over remineralization. Applying a previously published stoichiometric model, we observed a vertical fractionation of organic-matter remineralization. Although there is a preferential remineralization of proteins and P compounds in the entire domain of ENACW, the percentage was higher in the upper ENACW (σ<27.10 kg/m3) than in the lower; the percentage of N and P compounds in the oxidised organic matter was >80% for the upper ENACW and 63% for the lower. Likewise, the redissolution of calcareous structures contributes about 6% and 13% to the carbon regenerated in the upper and lower layers of ENACW, respectively. 相似文献
80.