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This paper is a follow-up to a previous paper on the subject of liquefaction potential index (LPI), a parameter that is often used to characterize the potential for surface manifestation of liquefaction at a given site subjected to a given shaking level (represented by a pair of peak ground surface acceleration amax and moment magnitude Mw). In the previous paper by Juang and his coworkers, the LPI was re-calibrated for a piezocone penetration test (CPTU) model, and a simplified model based on LPI was created for computing the conditional probability of surface manifestation of liquefaction (PG). In this paper, the model for this conditional probability PG is extended into a complete framework for assessing the probability of surface manifestation of liquefaction in a given exposure time at a given site subjected to all possible ground motions at all seismic hazard levels. This new framework is formulated and demonstrated with an example site in 10 different seismic regions in the United States. 相似文献
996.
New insights into the origin of perylene in geological samples 总被引:1,自引:0,他引:1
Kliti Grice Hong Lu Pia Atahan Muhammad Asif Paul Greenwood Ercin Maslen Kenneth Williford 《Geochimica et cosmochimica acta》2009,73(21):6531-6543
The origin of the polycyclic aromatic hydrocarbon (PAH) perylene in sediments and petroleum has been a matter of continued debate. Reported to occur in Phanerozoic organic matter (OM), fossil crinoids and tropical termite mounds, its mechanism of formation remains unclear. While a combustion source can be excluded, structural similarities to perylene quinone-like components present in e.g. fungi, plants, crinoids and insects, potentially suggest a product-precursor relationship. Here, we report perylene concentrations, 13C/12C, and D/H ratios from a Holocene sediment profile from the Qingpu trench, Yangtze Delta region, China. Perylene concentrations differ from those of pyrogenic PAHs, and rise to prominence in a stratigraphic interval that was dominated by woody vegetation as determined by palynology including fungal spores. In this zone, perylene concentrations exhibit an inverse relationship to the lignin marker guaiacol, D/H ratios between −284‰ and −317‰, similar to the methoxy groups in lignin, as well as co-variation with spores from wood-degrading fungi. 13C/12C of perylene differs from that of land plant wax alkanes and falls in the fractionation range expected for saprophytic fungi that utilise lignin, which is isotopically lighter than cellulose and whole wood. During progressive lignin degradation, the relative carbon isotopic ratio of the perylene decreases. We therefore hypothesise a relationship of perylene to the activity of wood-degrading fungi. To support our hypothesis, we analysed a wide range of Phanerozoic sediments and oils, and found perylene to generally be present in subordinate amounts before the evolutionary rise of vascular plants, and to be generally absent from marine-sourced oils, few exceptions being attributed perhaps to a contribution of marine and/or terrestrial-derived fungi, anoxia (especially under marine conditions) and/or contamination of core material by fungi. A series of low-molecular-weight aromatic quinones bearing the perylene-backbone were detected in Devonian and Cretaceous sediments, potentially representing precursor components to perylene. 相似文献
997.
Hong Lu Tengshui Chen Kliti Grice Paul Greenwood Ping’an Peng Guoying Sheng 《Organic Geochemistry》2009,40(8):902-911
An unusual series of C22–C27 monounsaturated sterenes and C24–C30 tetracyclic terpanes (17,21-secohopanes) were detected in relatively high concentrations in an immature evaporitic marl sediment of the Jinxian Sag, Bohai Bay Basin, North China. The site of unsaturation in these novel sterenes is assigned tentatively to the D ring on the basis of mass spectral interpretation, which also distinguishes them from reported unsaturated sterenes. Other hydrocarbon biomarker or stable isotope characteristics are indicative of microbial (e.g. methyl hopanes), phytoplankton or higher plant (depleted δ13C values of isoprenoids and hopanes) inputs and an anoxic carbonate depositional environment (hexacyclic hopanes; tetracyclic terpanes). The hydrocarbon composition showed no obvious biodegradation and the relatively high concentration of unsaturated terpenoids (e.g. gammacerene) and low values of other established maturity parameters (Ts/Tm = 0.23; Ro = 0.44%; Tmax = 417 °C), are consistent with sediments of low maturity. The novel, low molecular weight sterenes and the tetracyclic terpanes may be early diagenetic products of microbial sources in a carbonate environment. 相似文献
998.
黔西南白层超基性岩墙锆石SHRIMP U-Pb年龄和Hf同位素组成研究 总被引:14,自引:6,他引:8
文章对黔西南白层地区出露的燕山期超基性岩墙进行了单颗粒锆石SHRIMP U-Pb年龄和Hf同位素组成研究,获得A、B两组不同的锆石年龄.A组锆石呈不规则粒状,具不完整的宽大条带,12颗锆石的 SHRIMP U-Pb年龄加权平均值为(84±1)Ma,代表了超基性岩墙的侵位年龄;锆石Hf原位分析表明,176Hf/177Hf从0.282561到0282719,εHf(84 Ma)平均为-3.61,表明岩浆源区主要以富集地幔为主,并受到部分地壳物质的混染.B组锆石晶形完整,具典型的中酸性岩浆型振荡环带,3颗锆石的SHRIMP U-Pb模式年龄为409~450 Ma.176Hf/177Hf从0282379到0282440,εHf(t)平均为-3.77,均低于A组锆石,属于捕获锆石.据此认为84 Ma左右由于华南岩石圈伸展,软流圈地幔上涌,导致岩石圈富集地幔部分熔融,熔体上升过程中与409~450 Ma左右形成的少量地壳岩石发生混染,随后快速侵位冷凝而形成基性-超基性岩墙.白层地区84 Ma的超基性岩浆活动是整个华南西部燕山晚期(80~90 Ma)岩浆活动的一部分.右江褶皱带周缘的燕山晚期岩浆活动主要与大规模的Sn、W、Ag、Cu、Pb、Zn等矿床有关,但右江褶皱带内部的燕山晚期岩浆活动是否与以卡林型金矿为代表的低温热液矿床有成因上的联系,尚需更多矿床年代学资料的证实. 相似文献
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1000.
大庆长垣南部包括葡北、敖包塔和葡两3个局部构造.黑帝庙油层的形成与3种不同演化历史断层有关:反转期断裂(Ⅲ犁)、断陷期形成坳陷期和反转期均活动的断裂(Ⅰ-Ⅱ-Ⅲ型)和坳陷期形成反转期活动的断裂(Ⅱ-Ⅲ型);其中连通气源岩且活动期与大量生排气期相匹配的Ⅰ-Ⅱ-Ⅲ型和Ⅱ-Ⅲ型断裂是生物气垂向运移的主要通道,Ⅰ-Ⅱ-Ⅲ型断裂是深部CO2向上运移的主要通道.这些断层均是“似花状”断层组合的边界断层,对倾边界断层控制背斜和鼻状构造形成.数值模拟表明:对倾的气源断层与地层产状的配置关系共同控制天然气运移方向和聚集的部位,由于葡萄花和敖包塔构造西缓东陡,因此天然气主要富集在背斜东翼和背斜之间的断块上. 相似文献