首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   245篇
  免费   7篇
  国内免费   1篇
大气科学   13篇
地球物理   58篇
地质学   90篇
海洋学   31篇
天文学   40篇
自然地理   21篇
  2023年   1篇
  2021年   3篇
  2020年   7篇
  2018年   6篇
  2017年   8篇
  2016年   7篇
  2015年   9篇
  2014年   5篇
  2013年   9篇
  2012年   10篇
  2011年   26篇
  2010年   11篇
  2009年   16篇
  2008年   18篇
  2007年   14篇
  2006年   15篇
  2005年   10篇
  2004年   13篇
  2003年   13篇
  2002年   10篇
  2001年   3篇
  2000年   4篇
  1999年   3篇
  1998年   1篇
  1997年   6篇
  1996年   2篇
  1995年   2篇
  1994年   3篇
  1992年   1篇
  1991年   2篇
  1990年   1篇
  1989年   1篇
  1988年   1篇
  1987年   1篇
  1984年   3篇
  1983年   2篇
  1978年   1篇
  1977年   2篇
  1968年   1篇
  1967年   1篇
  1957年   1篇
排序方式: 共有253条查询结果,搜索用时 234 毫秒
51.
The antifouling boosting agent Irgarol 1051 is a strong inhibitor of the photosystem II (PSII) with high efficiency/toxicity towards algae. However, because some phytoplankton species are more sensitive to Irgarol than others, its persistent release into the environment could result in adverse changes in the phytoplankton community structure at heavily impacted sites such as marinas. Continuous monitoring in the Florida Keys showed Irgarol concentrations of up to 635 ngL(-1) in the canal system leading to Key Largo Harbor Marina (KLH) with a sharp decrease in concentration at stations offshore from the mouth of the canal. Preliminary phytoplankton community assessments from surface water samples collected in KLH between February and August 2004 showed changes in several phytoplankton species in concordance with the increase of the herbicide concentrations. Typical responses include an increase in the abundance of eukaryotes and Cryptomonas sp. as Irgarol concentrations increase.  相似文献   
52.
53.
Deep-fluids: Neptune meets Pluto   总被引:2,自引:0,他引:2  
  相似文献   
54.
1INTRODUCTION BARITE(BASO4)ISANEXTREMELYINSOLUBLESALT;THISAROUSESPROBLEMSINPETROLEUMINDUSTRYBECAUSE BASO4ISAPARTICULARLYINTRACTABLESCALINGAGENT.BARITE PRECIPITATIONINTHEWELLBOREENVIRONMENTGENERALLYRE QUIRESMECHANICALREMOVAL,WITHCONSIDERABLEASSOCIAT EDEXPE…  相似文献   
55.
56.
Summary The earthquakes of 19 September 1985 (18.2° N, 102.7° W and a magnitude of 8.1 Richter scale) and of 20 (17.6° N, 101.8° W and a magnitude of 7.5 Richter scale) September 1985, caused the total or partial destruction of more than 2000 structures in Mexico City. The most affected areas are located along the fringes of and bordering old roadways, earthworks (dikes), aquaducts and pre-hispanic population centres. Ancient construction artificially modified the sedimentation in the basin of the Mexico Valley Lakes making the sub-soil of Mexico City more rigid near to the surface, and producing deviations of the surface seismic waves (Rayleigh waves and Love waves). Also, when earthquakes occur on the Pacific coast, seismic waves travel quickly through plutonic, metamorphics and continental and marine rocks of different ages, having high seismic velocities. When the seismic waves enter the poorly consolidated lake sediments having low seismic velocities in the Mexico City Basin, they produce an energy buildup that causes the phenomenon called magnification.There exists a direct relation between the amplification mentioned above and the presence of rigid bodies that are buried in the sub-soil. The length of these bodies is of the order of tens of kilometres horizontally with thicknesses less than 50 metres. These Rigid Barriers produce reflections and refractions of the surface waves along their borders with destructive consequences for the buildings. A correlation between the buildings and the houses damaged and destroyed and the location of the prehispanic construction on the sub-soil has been made which shows that the most damage happened in the borders of old roadways (i.e. Tlalpan road), perimeter walls (i.e. San Lazaro), aqueducts (i.e. Chapultepec Avenue), pyramids (i.e. Templo Mayor) and population centres (i.e. Tlaltelolco).  相似文献   
57.
During the Mauna Ulu flank eruption on Kilauea, Hawaii, the concentrations in the lavas of the minor elements K, P, Na and Ti, and the incompatible trace elements (analyzed by isotope dilution) K, Rb, Cs, Ba, Sr, and the REE (except Yb) decreased monotonically and linearly with the time (or date) of the eruption. At the same time, the concentrations of the major elements and of Yb, and the ratios of K/Rb, K/Cs, Ba/Rb, 87Sr/86Sr and 143Nd/144Nd remained constant. Most of the scatter in the raw concentration data is removed by a simple correction for olivine (plus chromite) fractionation previously established by Wright et al. (1975). These results are explained by simple equilibrium partial melting of a uniform source. The degree of melting increased by about 20% of the initial value during the course of the eruption. The trace element data are inverted by the method originated by Minster and Allègre (1978) and simplified by Hofmann and Feigenson (1983). The source has the following element (or isotope) ratios: K/Rb=501±7, Ba/Rb=14.0±0.5, Rb/Cs=95±7, Rb/Sr=0.0193 (+0.0045, –0.0090), (Ce/Ba)CN= 1.1±0.1, (Sr/Ba)CN=1.19 (+0.30, –0.19), 87Sr/86Sr=0.703521±0.000016, and 143Nd/144Nd=0.512966±0.000008. The REE pattern of the source has a nearly flat or slightly negative slope (=relative LREE enrichment) between Ce and Dy and a strongly positive slope between Dy and Yb. However, this relative HREE enrichment is poorly constrained by the analytical data, is highly model dependent and may not be a true source feature. The Yb concentration in the source is particularly poorly constrained because it is essentially constant in the melts. On the other hand, this special feature demonstrates that Yb must be buffered by a mineral phase with a high partition coefficient for Yb, namely garnet. The calculated clinopyroxene/garnet ratio in the source is roughly equal to one. In contrast, the source of Kohala volcano had previously been found to contain little or no garnet.  相似文献   
58.
The trace element composition of silicate inclusions in diamonds: a review   总被引:1,自引:0,他引:1  
On a global scale, peridotitic garnet inclusions in diamonds from the subcratonic lithosphere indicate an evolution from strongly sinusoidal REEN, typical for harzburgitic garnets, to mildly sinusoidal or “normal” patterns (positive slope from LREEN to MREEN, fairly flat MREEN–HREEN), typical for lherzolitic garnets. Using the Cr-number of garnet as a proxy for the bulk rock major element composition it becomes apparent that strong LREE enrichment in garnet is restricted to highly depleted lithologies, whereas flat or positive LREE–MREE slopes are limited to less depleted rocks. For lherzolitic garnet inclusions, there is a positive relation between equilibration temperature, enrichment in MREE, HREE and other HFSE (Ti, Zr, Y), and decreasing depletion in major elements. For harzburgitic garnets, relations are not linear, but it appears that lherzolite style enrichment in MREE–HREE only occurs at temperatures above 1150–1200 °C, whereas strong enrichment in Sr is absent at these high temperatures. These observations suggest a transition from melt metasomatism (typical for the lherzolitic sources) characterized by fairly unfractionated trace and major element compositions to metasomatism by CHO fluids carrying primarily incompatible trace elements. Melt and fluid metasomatism are viewed as a compositional continuum, with residual CHO fluids resulting from primary silicate or carbonate melts in the course of fractional crystallization and equilibration with lithospheric host rocks.

Eclogitic garnet inclusions show “normal” REEN patterns, with LREE at about 1× and HREE at about 30× chondritic abundance. Clinopyroxenes approximately mirror the garnet patterns, being enriched in LREE and having chondritic HREE abundances. Positive and negative Eu anomalies are observed for both garnet and clinopyroxene inclusions. Such anomalies are strong evidence for crustal precursors for the eclogitic diamond sources. The trace element composition of an “average eclogitic diamond source” based on garnet and clinopyroxene inclusions is consistent with derivation from former oceanic crust that lost about 10% of a partial melt in the garnet stability field and that subsequently experienced only minor reenrichment in the most incompatible trace elements. Based on individual diamonds, this simplistic picture becomes more complex, with evidence for both strong enrichment and depletion in LREE.

Trace element data for sublithospheric inclusions in diamonds are less abundant. REE in majoritic garnets indicate source compositions that range from being similar to lithospheric eclogitic sources to strongly LREE enriched. Lower mantle sources, assessed based on CaSi–perovskite as the principal host for REE, are not primitive in composition but show moderate to strong LREE enrichment. The bulk rock LREEN–HREEN slope cannot be determined from CaSi–perovskites alone, as garnet may be present in these shallow lower mantle sources and then would act as an important host for HREE. Positive and negative Eu anomalies are widespread in CaSi–perovskites and negative anomalies have also been observed for a majoritic garnet and a coexisting clinopyroxene inclusion. This suggests that sublithospheric diamond sources may be linked to old oceanic slabs, possibly because only former crustal rocks can provide the redox gradients necessary for diamond precipitation in an otherwise reduced sublithospheric mantle.  相似文献   

59.
Mineralium Deposita - The massive sulfide deposits of the Kristineberg area, Sweden, occur within a 2- to 3-km-thick succession of felsic volcaniclastic rocks belonging to the Skellefte Group. The...  相似文献   
60.
We have measured 87Sr/86Sr and 143 Nd/144 Nd isotope ratios in different batches and aliquots of the new US Geological Survey (USGS) reference materials (RMs) BCR-2, BHVO-2, AGV-2 and GSP-2 and the original USGS RMs BCR-1, BHVO-1, AGV-1 and GSP-1 by thermal ionisation mass spectrometry. In addition, we also analysed the eight Max-Planck-Institut-Dingwell (MPI-DING) reference glasses. Nearly all isotope ratios obtained in the different aliquots and batches agree within uncertainty limits indicating excellent homogeneity of the USGS powders and the MPI-DING glasses. With the exception of GSP-2, the new USGS RMs are also indistinguishable from the ratios found in the original USGS RMs (87Sr/86Sr: 0.704960, 0.704958 (BCR-1, -2), 0.703436, 0.703435 (BHVO-1, -2), 0.703931, 0.703931 (AGV-1, -2); 143 Nd/144 Nd: 0.512629, 0.512633 (BCR-1, -2), 0.512957, 0.512957 (BHVO-1, -2); 0.512758, 0.512755 (AGV-1, -2)). This means that for normalisation purposes in Sr and Nd isotope geochemistry BCR-2, BHVO-2 and AGV-2 can well replace BCR-1, BHVO-1 and AGV-1 respectively.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号