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41.
We have investigated the N geochemistry of minerals and rocks from contact metamorphic aureoles and hydrothermal vent complexes (HVC) in the Karoo Basin in South Africa. The HVC formed during phreatic eruptions associated with rapid devolatilization and pressure build-up in contact aureoles around early Jurassic sill intrusions. By combining outcrop data from a HVC and core data from contact aureoles, we investigate the relationship between light element release during metamorphism and vertical fluid migration. Sandstone and breccia from the HVC contain early-diagenetic ammonium -bearing feldspar (buddingtonite) and illite. Ammonium occupies up to 95% of the A site in feldspar, corresponding to concentrations up to 5.2 wt% N. Bulk-rock N isotope data for rocks from inside and outside the hydrothermal vent complex fall into two distinct groups. Background samples have δ15Nair between +1.5‰ and +4.9‰, whereas minerals from the vent complex have δ15N in the range +7.5 to +10.6‰. The N geochemistry of contact metamorphic shale from the lower stratigraphic units of the Karoo Basin shows that the vitrinite reflectance and δ15N values are positively correlated. Shale with reflectivity values >4%Ro are enriched in 15N, with δ15N values between +6‰ and +14‰, implying the release of isotopically light N into metamorphic fluids (probably as N2). We suggest that the relatively high δ15N values of the early-diagenetic buddingtonite in the HVC reflect exchange of buddingtonite with N-bearing fluids ascending from greater depth after their release during contact metamorphism and dehydration. We present a qualitative model whereby hydrothermal vent complexes represent fluid flow structures after their formation, focusing N-bearing metamorphic fluids sourced in deeper levels of the basin. The release of organic N from sediments at depth in volcanic basins could play a role in the geochemical cycle of N, becoming particularly important during periods of intense volcanic activity.  相似文献   
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The free energy yield of microbial respiration reactions in anaerobic marine sediments must be sufficient to be conserved as biologically usable energy in the form of ATP. Anaerobic oxidation of methane (AOM) coupled to sulfate reduction (SRR) has a very low standard free energy yield of ΔG° = −33 kJ mol−1, but the in situ energy yield strongly depends on the concentrations of substrates and products in the pore water of the sediment. In this work ΔG for the AOM-SRR process was calculated from the pore water concentrations of methane, sulfate, sulfide, and dissolved inorganic carbon (DIC) in sediment cores from different sites of the European continental margin in order to determine the influence of thermodynamic regulation on the activity and distribution of microorganisms mediating AOM-SRR. In the zone of methane and sulfate coexistence, the methane-sulfate transition zone (SMTZ), the energy yield was rarely less than −20 kJ mol−1 and was mostly rather constant throughout this zone. The kinetic drive was highest at the lower part of the SMTZ, matching the occurrence of maximum AOM rates. The results show that the location of maximum AOM rates is determined by a combination of thermodynamic and kinetic drive, whereas the rate activity mainly depends on kinetic regulation.  相似文献   
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Two sites on the east coast of Sweden (Forsmark and Laxemar/Simpevarp) are currently being investigated as potential geologic hosts for a deep repository isolating high-level nuclear waste. In this paper, a methodology for fracture mineral studies is suggested with focus on the variation in depth of the fresh/saline water interface and location of the redox front in the bedrock. The most commonly precipitated fracture minerals in crystalline rocks are chlorite, calcite, quartz, K-feldspar, Ca–Al-silicates like epidote, prehnite and laumontite, sulphides and Fe-oxides. Of these, calcite is the mineral best suited for palaeohydrological studies since it precipitates during a wide range of conditions including low-temperature conditions during the Pleistocene and Holocene epochs. Sulphides and Fe-oxides/hydroxides provide information on the position of the redox front. In order to carry out palaeohydrological studies, a number of prerequisites are required such as; high quality drill core material, geological knowledge of the sequence of fracture mineralizations; the post-glacial (Holocene) evolution in the area; high quality groundwater chemistry, including stable isotopes; and a conceptual model of the hydrogeochemistry that is to be tested. The choice of methods used here is based on the fact that both the Forsmark and Laxemar/Simpevarp sites are situated in Palaeoproterozoic crystalline rocks with reactivation of fractures over at least 1.5 Ga, and they have been exposed to glaciations/deglaciations and transgressions/regressions of the Baltic Sea during the Quaternary. This has resulted in a palaeohydrology with a range of groundwaters of quite different chemistry and stable isotopic composition. The suggested scheme for solving the variation in depth of the fresh/saline water interface focuses on fracture calcite. It includes a step-by-step procedure with;
(1)
Initial δ18O and δ13C, analyses and complementary petrographic studies of thin sections and crystal morphology followed by  相似文献   
44.
Zircon U–Pb geochronometry, heavy mineral analyses and conventional seismic reflection data were used to interpret the provenance of the Lower Triassic Bunter Sandstone Formation. The succession was sampled in five Danish wells in the northern part of the North German Basin. The results show that sediment supply was mainly derived from the Ringkøbing‐Fyn High situated north of the basin and from the Variscan belt located south of the basin. Seismic reflection data document that the Ringkøbing‐Fyn High was a local barrier for sediment transport during the Early Triassic. Hence, the Fennoscandian Shield did not supply much sediment to the basin as opposed to what was previously believed. Sediment from the Variscan belt was transported by wind activity across the North German Basin when it was dried out during deposition of the aeolian part of the Volpriehausen Member (lower Bunter Sandstone). Fluvial sand was supplied from the Ringkøbing‐Fyn High to the basin during precipitation events which occurred most frequently when the Solling Member was deposited (upper Bunter Sandstone). Late Neoproterozoic to Carboniferous zircon ages predominate in the Volpriehausen Member where the dominant age population with a peak age of 337 Ma corresponds to the culmination of Variscan high‐grade metamorphism, whereas a secondary age population with a peak at 300 Ma matches the timing of volcanism and magmatism at the Carboniferous/Permian boundary in the northern Variscan belt. Parts of the basement in the Ringkøbing‐Fyn High were outcropping during the Early Triassic and zircon ages similar to this Mesoproterozoic basement are present in the Bunter Sandstone. The heavy mineral assemblage of the Solling Member is uniform and has a high garnet content compared to the contemporaneous sediments in the Norwegian‐Danish Basin and in the southern part of the North German Basin. This finding confirms that a local source in the Ringkøbing‐Fyn High supplied most of the fluvial sediment in the northern part of the North German Basin. The northernmost part of the Bunter Sandstone is situated on a platform area that is separated from the basin area by a broad WNW–ESE‐oriented fault zone. The most promising reservoir in the basin area is the aeolian Volpriehausen Member since the sandstone has a wide lateral distribution and a constant thickness. The alluvial to ephemeral fluvial Solling Member may be a good reservoir in the platform area and marginal basin area, but the complex sand‐body architecture makes it difficult to predict the reservoir quality.  相似文献   
45.
A dravite from Yemen of near end-member composition was treated in air and hydrogen atmospheres at 600–900 °C to reveal changes in Mg and Al order over the octahedrally coordinated Y and Z sites, and to explore related changes in the characteristic vibrational bands in the principal (OH)-stretching frequency. Relevant information was obtained using electron microprobe analysis (EMPA), structural refinement (SREF) and polarized infrared (IR) single-crystal spectroscopy. Overall, the EMPA, SREF and IR data show that only minor changes occur during thermal treatment up to at least 800 °C, including variations in structural parameters, Mg–Al order–disorder and (OH)-stretching bands, indicating limited hydrogen loss. Untreated and treated dravite samples have very similar long-range and short-range atomic structures, which may be related to the occurrence of stable Al–Mg extended clusters around the O1 (=W) and O3 (=V) sites: W(F)–Y(MgMgMg)–V(OH)3Z[AlAlAlAlAl(Al,Mg)]; W(OH)–Y(MgMgAl)–V(OH)3Z[AlAlAlAlAl(Al,Mg)]; W(O2–)–Y(AlAlAl)–V(OH)3Z[AlAlAlAlAl(Al,Mg)]. These extended clusters remain stable to temperatures close to the observed start of decomposition (~900 °C).  相似文献   
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An estimate of the total biomass of fish in the North Sea   总被引:2,自引:4,他引:2  
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