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181.
 Kuju Volcano lies near Aso Caldera at the center of Kyushu Island, western Japan. After a few hundred years of dormancy, a phreatic explosion accompanied by a small ash eruption occurred on 11 October 1995. This study was undertaken to determine the subsurface seismic velocity structure associated with the active magmatic regime in the Kuju volcanic region. The three-dimensional, upper crustal, P-wave velocity structure beneath Kuju Volcano was determined using methods for the simultaneous inversion of P-wave arrival times from local earthquakes in and around the Kuju volcanic region for velocities and hypocentral parameters. Results reveal two shallower low-velocity anomalies located in the northern and southern parts of Kuju Volcano, consistent with the presence of significant negative Bouguer gravity anomalies. In addition, a high-velocity anomaly is located approximately 5 km northwest of Mt. Kuju, one of the domes in Kuju Volcano. Beneath this high-velocity anomaly, a low-velocity anomaly is present. This velocity structure suggests a magmatic regime that has a lid consisting of cooled solid material overlying a chamber of partially molten material. Received: 23 September 1997 / Accepted: 20 June 1998  相似文献   
182.
Partitioning of copper, zinc, iron and manganese into oxide, sulfide, organic and silicate fractions has been determined with a selective chemical leaching technique on sediment samples from a core collected in Osaka Bay. The samples have been dated by the210Pb method. Most of the copper and zinc in the polluted surface sediment layer are contained in both oxide and sulfide fractions. This suggests that the transformation of oxides and hydroxides to sulfides under anoxic conditions within the sediment is significant for the fixation of copper and zinc discharged through human activities into the sediment. Manganese is apparently enriched in oxide and hydroxide fractions of the surface layer due to the post-depositional migration of manganese within the sediment. The copper, zinc and manganese contents of the 30 % H2O2 soluble fraction (mostly organic fraction) decrease with depth in the sediment core, and correlate significantly with the organic carbon content. The heavy metal (Cu, Zn, Fe and Mn) contents of the silicate fraction, without exchangeable sites, are almost constant with depth.  相似文献   
183.
Experiments with a set of electrolyte solutions have been carried out to investigate the effects of pore water composition changes on the stability conditions of methane hydrate in marine sediments. The results reveal that (1) SO42− and Cl concentration changes can affect hydrate stability slightly, (2) the changes in both the type and the concentration of cations, which occur in normal diagenetic processes, do not exert a significant influence on the methane hydrate stability conditions, and (3) the shift of hydrate stability in pore water can be expressed as a function of the Cl concentration only. Based on the results above, an empirical equation ΔT (K)=0.00206 Cl (mmol/dm3) has been obtained for estimating the shift in the equilibrium temperature of methane hydrate in pore water at a given pressure.  相似文献   
184.
在日本海会聚边缘的东侧,第三纪沉积物厚度大、有机质丰富,是日本最好的油气区。2003—2004年,在对该区南部的Naoetsu盆地中的UT-04海岭进行调查时,日本METI和JOG-MEC意外地发现了与气体活动有关的较大的麻坑、浅表层含气沉积物以及充气泥丘。高精度地震调查证实海底之下约170  相似文献   
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186.
The annual flux of biologically produced organic carbon from surface waters is equivalent to annual net community production (NCP) at a steady state and equals the export of particulate and dissolved organic carbon (POC and DOC, respectively) to the ocean interior. NCP was estimated from carbon budgets of salinity-normalized dissolved inorganic carbon (nDIC) inventories at two time-series stations in the western subarctic (K2) and subtropical (S1) North Pacific Ocean. By using quasi-monthly biogeochemical observations from 2004 to 2013, monthly mean nDIC inventories were integrated from the surface to the annual maximum mixed layer depth and corrected for changes due to net air–sea CO2 exchange, net CaCO3 production, vertical diffusion from the upper thermocline, and horizontal advection. The annual organic carbon flux at K2 (1.49 ± 0.42 mol m?2 year?1) was lower than S1 (2.81 ± 0.53 mol m?2 year?1) (p < 0.001 based on t test). These fluxes consist of three components: vertically exported POC fluxes (K2: 1.43 mol m?2 year?1; S1: 2.49 mol m?2 year?1), vertical diffusive DOC fluxes (K2: 0.03 mol m?2 year?1; S1: 0.25 mol m?2 year?1), and suspended POC fluxes (K2: 0.03 mol m?2 year?1; S1: 0.07 mol m?2 year?1). The estimated POC export flux at K2 was comparable to the sum of the POC flux observed with drifting sediment traps and active carbon flux exported by migrating zooplankton. The export fluxes at both stations were higher than those reported at other time-series sites (ALOHA, the Bermuda Atlantic Time-series Study, and Ocean Station Papa).  相似文献   
187.
Drifting sediment trap experiments were conducted during various seasons to elucidate the characteristics of particles sinking through the upper 200 m of the water column in the western Pacific at subarctic station K2 and subtropical station S1. The sinking particle flux increased when primary productivity was high at each station, during June–July at K2 and during February at S1. Biogenic opal (Opal) and CaCO3 were the major components of the fluxes at K2 and S1, respectively. Contrary to the expectation of a high flux at the eutrophic station K2 and low flux at the oligotrophic station S1, the annual average organic carbon fluxes at 100 m were comparable at both stations: 62.7 mg C m?2 day?1 at K2 and 56.1 mg C m?2 day?1 at S1. The similarity of the fluxes was perhaps a reflection of the unexpectedly high primary production at S1. At K2, the organic carbon export ratio (organic carbon flux/primary productivity) was significantly and negatively correlated with primary production and tended to decrease with depth. The magnitude of the rate of attenuation of the organic carbon flux with depth was larger at S1 than at K2. This rate of attenuation tended to decrease and increase with primary production at K2 and S1, respectively. The explanation for these patterns may be that the flux of labile organic carbon at relatively shallow depths decreased with increasing primary production at K2, and zooplankton grazing pressure increased with increasing primary productivity at S1.  相似文献   
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189.
Summary High-grade blocks in the Franciscan complex at Tiburon, California, record relatively low temperature eclogite-facies metamorphism and blueschist-facies overprinting. The eclogite-facies mineral assemblage contains prograde-zoned garnet + omphacite + epidote ± hornblende (katophoritic and barroisitic Ca–Na amphibole) ± glaucophane + phengite (∼3.5 Si p.f.u.) ± paragonite + rutile + quartz. The blueschist-facies mineral assemblage contains chlorite + titanite + glaucophane + epidote ± albite ± phengite (∼3.3 Si p.f.u.). Albite is not stable in the eclogite stage. New calculations based on garnet-omphacite-phengite thermobarometry and THERMOCALC average-PT calculations yield peak eclogite-facies PT conditions of P = 2.2–2.5 GPa and T = 550–620 °C; porphyroclastic omphacite with inclusions of garnet and paragonite yields an average-PT of 1.8 ± 0.2 GPa at 490 ± 70 °C for the pre-peak stage. The inferred counterclockwise hairpin PT trajectory suggests prograde eclogitization of a relatively “cold” subducting slab, and subsequent exhumation and blueschist-facies recrystallization by a decreasing geotherm. Although an epidote-garnet amphibolitic assemblage is ubiquitous in some blocks, PT pseudosection analyses imply that the epidote-garnet amphibolitic assemblage is stable during prograde eclogite-facies metamorphism. Available geochronologic data combined with our new insight for the maximum pressure suggest an average exhumation rate of ∼5 km/Ma, as rapid as those of some ultrahigh pressure metamorphic terranes.  相似文献   
190.
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