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21.
Kimberly K. Takagi Phaothep Cherdsukjai Izumi Mimura Yuka Yano Kanjana Adulyanukosol Makoto Tsuchiya 《Estuarine, Coastal and Shelf Science》2010
This study aimed to elucidate Dotilla myctiroides (H. Milne-Edwards) food resources and how the soldier crab influences the organic matter composition on the intertidal flat. A preliminary assessment of D. myctiroides size, sex, and population distribution was conducted to clarify the characteristics of the inhabiting population. Overall, D. myctiroides size and abundance was normal across the tidal flat area. Comparison of different sediment types from the soldier crab habitat (surface sediments, igloos, burrow lining, burrow pellets, feeding pellets, and feces) using the fatty acid (FA) analysis technique revealed D. myctiroides removes organic matter via the significantly lower contributions of polyunsaturated FAs, essential FAs, and dinoflagellates in the feeding pellets. Dotilla myctiroides tissue analysis of the hepatopancreas and hindgut in individuals that had been starved for 24 h confirmed not only the consumption of dinoflagellates, but diatoms and macroalgae as well. In addition, the FA metabolism within the digestive system implied the ability of the soldier crab to synthesize highly unsaturated FAs (HUFAs) such as 20:4n–6, 20:5n–3 and 22:6n–3. 相似文献
22.
A new method for the quantification of different redox-species of molybdenum (V and VI) in seawater 总被引:1,自引:0,他引:1
A new method for the direct determination of reduced and oxidized Mo species (Mo (V) and Mo (VI)) in seawater was developed and used for the first time. The method includes the complexation of Mo (V) with tartrate, solid phase extraction of the Mo (V)–tartrate complex by a XAD 7HP resin, followed by elution with acidic acetone. In this study, the eluted Mo (V) was quantified by graphite furnace atomic absorption spectrometry. The detection limit of this protocol was on the order of 0.2 nM. The analytical precision was 10% of ~ 10 nM. This method was successfully applied to the determination of Mo (V) and Mo (VI) in surface and bottom waters at the head of Peconic River Estuary. Total Mo (Mo (V) + Mo (VI)) ranged from 100–120 nM in most bottom saline waters, and 2.5–15 nM for surface fresher waters. Concentrations of Mo (V) in these environments ranged from 0 nM to ~ 15 nM, accounting for 0%–15% of the total dissolved Mo pool. The time series experiments showed that the Mo speciation changed within 1 h after the water collection, and therefore it is strongly suggested that speciation analysis be carried out within the first 15 min. However, since these are the first Mo speciation data in concentration ranges typical of normal marine and coastal waters, additional research may be required to optimize the methodology and further explore Mo cycling mechanisms. 相似文献
23.
PANG Jungang LI Wenhou XIAO Li. School of Petroleum Resources Xi'an Shiyou University Xi'an China. Geological Department Northwest University Xi'an China. State Key Laboratory of Continental Dynamics China. Geological Research Institute of Shengli Oilfield Co. Ltd. SINOPEC Dongying Sh ong China 《东北亚地学研究》2009,(4):183-188
Lacustrine turbidite of Chang-7 Member in the studied area consists of sihstone and fine sandstone with respect to grain size, which is feldspathic lithie sandstone, syrosem arkose and arkose with respect to mineral constitution affected by provenance. There are such apparent signatures as lithology, sedimentary structure, sedimentary sequence and well logs, to recognize turbidite. During the paleogeographic evolution of Chang-7 Member, lake basin and deep lake are both at their maximum extent during Chang-73 stage, resulting in the deposition of Zhangjiatan shale with widespread extent and of turbidite with fragmental-like. Deep lake line is gradually moving toward lake center and turbidite sand bodies are gradually turning better with better lateral continuity, connectivity and more thickness, from stages of Chang-73, Chang-72 and Chang-7t, which can be favorable reservoir in deep-water. 相似文献
24.
松辽盆地西部斜坡区烃渗漏蚀变信息遥感探测 总被引:2,自引:0,他引:2
使用陆地卫星ETM+7图像对松辽盆地西部斜坡区进行稠油探测,图像增强方法有主成分分析、波段比值和假彩色合成等.主成分因子1,3,4,5-PC3(1,3,4,5主成分分析的第3主成分),1,3,5,7-PC3,2,3,5,7-PC3和3,4,5,7-PC4与波段比值3/1,4/3,7/5和(4/3)-(2/3)等用丁假彩色合成,在合成影像上圈定烃渗漏蚀变区域.结果表明烃渗漏蚀变区域与地质背景密切相关,与下伏油藏的分布大致相符. 相似文献
25.
本文以地震频次作为地震活动的变量,通过自然正交函数展开方法,计算中国大陆7级以上强震前的地震活动频次场,提取出强震前时间因子和空间等值线的异常。结果表明,强震前时间因子出现超过均方差的高值或低值异常,异常多数分布在频次场的前4个典型场,具有多分量特点,第1个典型场异常贡献率最大(占总场40%~60%),绝大部分强震前5~8年出现长期异常,部分强震前1~2年出现中期异常,少数强震前3月出现短临异常的特征。区域频次等值线出现的高梯度旋涡区域是异常危险区,等值线值大于0.9且具有活动构造的危险区往往是强震的发震位置。另外,地震频次场与传统方法的区域地震活动频次(3月)震例对比,表明频次场时间因子异常具有自己的独特优越性和缺陷,并讨论了这些方法的差异性。 相似文献
26.
柴达木盆地北缘冷湖七号构造油气成藏过程与模式 总被引:9,自引:2,他引:7
本文在对冷湖七号油气成藏条件综合分析的基础上,依据构造发育史与烃源岩生、排烃史,结合流体包裹体均一温度,分析了冷湖七号构造油气藏形成期次和过程,总结了东、西2个构造高点的油气成藏模式。研究结果表明:①冷七1井N12层包裹体主要为含烃盐水包裹体和气态烃有机包裹体,其均一温度明显分为60~70℃和110~130℃两个峰值区,对应地质时间分别为N21—N22时期和N2末—现今。结合源岩生、排烃史和构造演化史分析表明N12—N22时期为冷湖七号油气成藏的主要时期;②冷湖七号东高点N21气藏形成机理与模式为:断控同生隆起—单源供烃—不整合、断裂输导—浮力驱动—次生型断裂遮挡油气成藏模式;西高点E3油藏形成机理与模式为:同生隆起—双源供烃—不整合、断裂输导—浮力驱动—残留型原生油藏成藏模式。 相似文献
27.
本文研究了在pH 6.5-7.8的(CH_2)_6N_4-HCl缓冲介质中,CDMAA和TritonX-100对Ga与o-Cl-PF和F~-显色反应的增敏作用。结果表明,Ga-o-Cl-PF-F-CDMAA-TritonX-100多元配合物λ_(max)为565nm,表观摩尔吸光系数ε=1.74×10~5L·mol~(-1)·Cm~(-1),Ga含量在0~6.0μg/25ml范围内符合比尔定律,用合成样和标样进行本方法考验,结果满意。 相似文献
28.
Nitrogen and sulfur species in Antarctic aerosols at Mawson,Palmer Station,and Marsh (King George Island) 总被引:4,自引:0,他引:4
D. L. Savoie J. M. Prospero R. J. Larsen F. Huang M. A. Izaguirre T. Huang T. H. Snowdon L. Custals C. G. Sanderson 《Journal of Atmospheric Chemistry》1993,17(2):95-122
High volume bulk aerosol samples were collected continuously at three Antarctic sites: Mawson (67.60° S, 62.50° E) from 20 February 1987 to 6 January 1992; Palmer Station (64.77° S, 64.06° W) from 3 April 1990 to 15 June 1991; and Marsh (62.18° S, 58.30° W) from 28 March 1990, to 1 May 1991. All samples were analyzed for Na+, SO
4
2–
, NO
3
–
, methanesulfonate (MSA), NH
4
+
,210Pb, and7Be. At Mawson for which we have a multiple year data set, the annual mean concentration of each species sometimes vary significantly from one year to the next: Na+, 68–151 ng m–3; NO
3
–
, 25–30 ng m–3; nss SO
4
2–
, 81–97 ng m–3; MSA, 19–28 ng m–3; NH
4
+
, 16–21 ng m–3;210Pb, 0.75–0.86 fCi m–3. Results from multiple variable regression of non-sea-salt (nss) SO
4
2–
with MSA and NO
3
–
as the independent variables indicates that, at Mawson, the nss SO
4
2–
/MSA ratio resulting from the oxidation of dimethylsulfide (DMS) is 2.80±0.13, about 13% lower than our earlier estimate (3.22) that was based on 2.5 years of data. A similar analysis indicates that the ratio at Palmer is about 40% lower, 1.71±0.10, and more comparable to previous results over the southern oceans. These results when combined with previously published data suggest that the differences in the ratio may reflect a more rapid loss of MSA relative to nss SO
4
2–
during transport over Antarctica from the oceanic source region. The mean210Pb concentrations at Palmer and Marsh and the mean NO
3
–
concentration at Palmer are about a factor of two lower than those at Mawson. The210Pb distributions are consistent with a210Pb minimum in the marine boundary layer in the region of 40°–60° S. These features and the similar seasonalities of NO
3
–
and210Pb at Mawson support the conclusion that the primary source regions for NO
3
–
are continental. In contrast, the mean concentrations of MSA, nss SO
4
2–
, and NH
4
+
at Palmer are all higher than those at Mawson: MSA by a factor of 2; nss SO
4
2–
by 10%; and NH
4
+
by more than 50%. However, the factor differences exhibit substantial seasonal variability; the largest differences generally occur during the austral summer when the concentrations of most of the species are highest. NH
4
+
/(nss SO
4
2–
+MSA) equivalent ratios indicate that NH3 neutralizes about 60% of the sulfur acids during December at both Mawson and Palmer, but only about 30% at Mawson during February and March. 相似文献
29.
30.