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41.
Akira Imai Yukiko Ohbuchi Takayuki Tanaka Seiya Morita Kentaro Yasunaga 《Resource Geology》2007,57(4):374-385
The porphyry Cu deposits at Waisoi in Namosi district, Viti Levu are separated into two deposits: the Waisoi East deposit and the Waisoi West deposit. In the Waisoi East deposit, quartz porphyry is exposed and in the Waisoi West deposit, diorite porphyry is sporadically exposed in addition to a small body of quartz porphyry. The mineralization in the Waisoi East deposit is characterized by the bornite–chalcopyrite–pyrite assemblage associated with traces of molybdenite and native gold. Polyphase fluid inclusions in stockwork quartz veinlets show homogenization temperatures ranging from 210 to >500°C. The high‐grade Cu mineralization in the Waisoi West deposit is characterized by the bornite–chalcopyrite–pyrite assemblage accompanied with sheeted and stockwork quartz veinlets. Polyphase fluid inclusions occasionally containing hematite flakes in quartz veinlets in the center of the Waisoi West deposit homogenize at temperatures ranging from 450°C to >500°C. However, fluid inclusions in stockwork quartz veinlets in the periphery, homogenize at lower temperatures around 210°C. Both in the Waisoi East and Waisoi West deposits, primary bornite–chalcopyrite–pyrite assemblage in the high Cu‐grade zone was deposited at the upper stability limit of chalcopyrite with respect to sulfur fugacity. Thus, the principal Cu mineralization at the Waisoi deposits occurred at a relatively high sulfur fugacity, that is, in a high‐sulfidation environment. 相似文献
42.
Uranium in coastal sediments of Tokyo Bay and Funka Bay 总被引:2,自引:0,他引:2
Shizuo Tsunogai Seiya Nagao Shintaro Watanabe Yoshiaki Takahashi Kazunari Suzuki Masatoshi Yamada Koh Harada 《Journal of Oceanography》1990,46(5):211-218
The sediment cores from Tokyo Bay and Funka Bay were analyzed for U and its isotopic ratio,234U/238U, after dissolving them in 0.1 M HCl, and 30% H2O2 in 0.05 M HCl. A small fraction of U in the anoxic sediments was dissolved in 0.1M HCl and even the added yield tracer,232U, was lost. The isotopic ratio of H2O2 soluble U in the sediments was equal to that of seawater, suggesting that the H2O2 soluble U in the sediments is authigenic. The 6M HCl solution dissolved part of the lithogenic U besides the authigenic U. The depth profiles of U from the two bays resembled each other. The authigenic U comprised more than half of the total U even at the surface and increased with depth down to 70 cm, showing small maxima at about 20 cm. The concentration of refractory U was nearly constant with depth and similar to that of the pelagic sediments. The highest U concentration, 6 µg g–1 which was about 5 times that of the pelagic sediments, was observed in the layer between 70 and 160 cm depth in Tokyo Bay. The annual sedimentation rates of U in the Tokyo Bay sediments were 2.6 tons at the surface and 7.0 tons at the 70–160 cm depth. The increase in U with depth should be due to the deposition of interstitial U either diffusing downward from the surface indicating the trapping of seawater U, or otherwise diffusing upward from the deeper layer indicating the internal cycling of U within the sediments. 相似文献
43.
Yasuko?Okuyama-KusunoseEmail author Toshiro?Morikiyo Akiko?Kawabata Akira?Uyeda 《Contributions to Mineralogy and Petrology》2003,145(5):534-549
Carbon isotope fractionation between coexisting calcite and graphite (C ) has been studied in metamorphosed limestones from three thermal aureoles around Cretaceous granitic bodies (i.e., Tanohata, Tono, and Senmaya aureoles) in the Kitakami Mountains, Northeast Japan. C in each aureole decreases toward the granitic bodies, and becomes virtually uniform near the sillimanite isograd for metapelites, although calcite has variable isotopic ratios reflecting the original sedimentary compositions. The relationships indicate that isotopic equilibrium has been attained in metamorphosed limestone of sillimanite grade. Estimated C at the sillimanite isograd is similar in the Tanohata and Tono aureoles, but different in the Senmaya aureole with smaller carbon isotopic fractionations. From the temperature dependence of C and the negative dP/dT of andalusite–sillimanite equilibrium, we conclude that the sillimanite isograd in the Senmaya aureole was under higher temperature and lower pressure than in the other two localities. Temperatures at the sillimanite isograd are estimated by using existing calibrations of carbon isotopic exchange between calcite and graphite, whereas pressures are estimated from carbon isotopic temperatures and the andalusite–sillimanite equilibrium (Holdaway and Mukhopadhyay 1993a). Consistency of the P–T estimates is examined in the light of phase equilibria in the pelitic system. The estimated pressures at the sillimanite isograd are at about 2.1–2.7(±0.2) kbar for the Tanohata and Tono aureoles and less than 1 kbar for the Senmaya aureole, respectively. Geobarometry of sillimanite isograd in thermal aureoles indicates a marked difference in the depth of solidification of upper crustal granitoids: the Senmaya pluton has intruded and solidified at a very shallow level of less than 4 km whereas the Tanohata and Tono plutons are more deep-seated (ca. 8–10 km). The method can also be an effective tool in studying low-pressure type metamorphism in which geothermobarometry using garnet is not always applicable.Editorial responsibility: J. Hoefs 相似文献
44.
45.
Variation of dissolved organic matter and fluorescence characteristics before,during and after phytoplankton bloom 总被引:3,自引:0,他引:3
Marut Suksomjit Seiya Nagao Kazuhiko Ichimi Tatsuo Yamada Kuninao Tada 《Journal of Oceanography》2009,65(6):835-846
The variation of dissolved organic matter (DOM) and fluorescence characteristics during the phytoplankton bloom were investigated
in Yashima Bay, at the eastern part of the Seto Inland Sea, Japan. We found significant accumulations of dissolved organic
carbon (DOC), dissolved organic nitrogen (DON), chromophoric dissolved organic matter (CDOM) fluorescence, and UV260 during the phytoplankton bloom period in 2005, although lower accumulations of DOC and DON and only increases of CDOM fluorescence
were observed during the bloom period in 2006. Little or no correlation between DOM and phytoplankton abundance might be due
to the composition of DOM, which is a complex mixture of organic materials. The 3D-EEM results revealed that the DOM produced
around the phytoplankton bloom period contained tyrosine, tryptophan, and humic-like substances. Our results showed that the
occurrence of phytoplankton bloom contributed to the production of DOM in coastal water but the DOM accumulation depended
on the type of phytoplankton bloom, the phytoplankton species in particular. From our results, we concluded that phytoplankton
have a great role in the dynamics of DOM as a producer in a coastal environment. 相似文献