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21.
Abstract. The Mutnovskoe deposit located in the Porozhisto‐Asachinskaya metallogenic province of South Kamchatka, Russia, is a polymetallic vein and Au‐Ag quartz vein associated type of hydrothermal deposit. The Mutnovskoe deposit is located inside a paleo‐caldera structure at the center of the Mutnovsko‐Asachinskaya geothermal field of Pliocene ‐ Quaternary age, where active gold deposition is identified in hot spring precipitate. The Mutnovskoe deposit is subdivided into the north flank, the central flank and the south flank based on the vein distributions and mineral parageneses. The mineralized vein system is oriented N‐S hosted in diorite ‐ gabbroic diorite stock, volcanic rocks and sedimentary rocks of Miocene ‐ Pleistocene age. The mineralization stage I (polymetallic vein) mainly in the central and the south flanks is Zn‐Pb‐Cu‐Au‐Ag contained in sphalerite, galena and tetrahedrite‐tennantite group mineral. The stage II (Au‐Ag quartz vein) occurs in the north and the central flanks. The stage III (Mn‐sulfide and Mn‐Ca‐carbonate vein) occurs in the whole deposit area. Stage II is the typical Au‐Ag quartz‐adularia vein of low‐sulfidation type. Stage III is alabandite‐rhodochrosite‐quartz‐calcite vein. The K‐Ar ages are 1.3±0.1 Ma for stage I sericite in alteration zone, and 0.7±0.1 Ma for the stage II adularia in mineralized vein. Based on the fluid inclusion study, range of ore forming temperature of the Mutnovskoe deposit is 200 to 260d?C (av. 230d?C). Salinities of fluid inclusions indicate 2.2 to 5.7 wt% NaCl in sphalerite and 0.8 to 3.3 wt% NaCl in quartz for the stage I. Mineral paragenesis of the polymetallic vein (stage I) is characterized by a district zoning of tennantite and Cd‐rich sphalerite in the south flank and tetrahedrite and Mn‐rich sphalerite in the central flank, which is due to the fractional crystallizations of ore‐forming fluid. Depositional condition of the low sulfidation state is inferred for the Mutnovskoe deposit, where the polymetallic vein of the south flank is in relatively higher sulfidation state than the central flank.  相似文献   
22.
The fate of Polycyclic Aromatic Hydrocarbons (PAHs) residing in the atmosphere has received enormous attention in recent years due to their mutagenic and carcinogenic risks on human health. In this context, the stability of pyrene (as a representative PAHs) on quartz, alumina, montmorillonite, kaolinite, humic acid and quartz coated with sorbed humic acid was investigated at controlled relative humidity (RH: i.e. 5% and 30%) without light irradiation in order to detect the presence of catalytic effect of mineral surface on PAHs decomposition. The stability of pyrene was found to depend strongly on the physicochemical properties of the substrates. Quartz showed a strong catalytic effect for the decomposition of pyrene even though it was coated with sorbed humic acid. Pyrene sorbed on montmorillonite and humic acid remained stable during the experimental period (i.e. 3 days). Moisture in the experimental cell also affected the stability of pyrene in particular minerals. Especially, pyrene sorbed on alumina was rapidly decomposed at higher RH. However, there were almost no effect in the case of quartz, kaolinite and humic acid. Depending on the physicochemical properties of aerosols and RH, PAHs associated with minerals in the atmosphere would be decomposed and/or stably reside in the atmosphere.  相似文献   
23.
We determined the partition coefficients of 19 elements between metallic liquid and silicate liquid at 20 GPa and 2500°C, and between metallic liquid and silicate perovskite at 27 GPa and 2200°C. Remarkable differences were observed in the partitioning behaviors of Si, P, W, Re, and Pb among the silicate liquid, perovskite, and magnesiowüstite coexisting with metallic liquid, reflecting incompatibility of the elements in the silicate or oxide phase. We could not observe any significant difference in the partitioning behaviors of V, Cr, Mn, Co, Ni, and Cu among the phases coexisting with metallic liquid.

Comparison of the present partitioning data with those obtained previously at lower pressure and temperature suggests that the exchange partition coefficients, Kmet/sil, of Co, Ni, Mo, and W decrease, whereas those of V, Cr, and Mn increase and tend to approach unity with increasing pressure and temperature. We also made preliminary experiments to clarify the effect of sulfur on the partitioning behaviors. Sulfur lowers the exchange partition coefficients, Kmet/sil, of Mo and W between metallic liquid and silicate liquid significantly at 20 GPa and 2300°C.

The mantle abundances of Co, Ni, Cu, Mo, and W calculated for the metal-silicate equilibrium model are lower than those of the real mantle, whereas P, K, and Mn are overabundant in the calculated mantle. The discrepancies in the abundances of Co and Ni could be explained by the chemical equilibrium at higher pressure and temperature. Large discrepancies in Mo and W between the calculated and real mantles could be accounted for by the effect of sulfur combined with the effects of pressure and temperature on the chemical equilibrium. The mantle abundances of P, K, and Cu could be accounted for by volatile loss in the nebula, perhaps before accretion of the Earth, combined with the chemical equilibrium at higher pressure and temperature. Thus the observed mantle abundances of P, K, Co, Ni, Cu, Mo, and W may be consistent with a model of sulfur-bearing metal-silicate equilibrium in lower-mantle conditions.  相似文献   

24.
25.
Landslides - A Correction to this paper has been published: https://doi.org/10.1007/s10346-021-01642-4  相似文献   
26.
Mineralogic studies of major ore minerals and fluid inclusion analysis in gangue quartz were carried out for the for the two largest veins, the Aginskoe and Surprise, in the Late Miocene Aginskoe Au–Ag–Te deposit in central Kamchatka, Russia. The veins consist of quartz–adularia–calcite gangue, which are hosted by Late Miocene andesitic and basaltic rocks of the Alnei Formation. The major ore minerals in these veins are native gold, altaite, petzite, hessite, calaverite, sphalerite, and chalcopyrite. Minor and trace minerals are pyrite, galena, and acanthine. Primary gold occurs as free grains, inclusions in sulfides, and constituent in tellurides. Secondary gold is present in form of native mustard gold that usually occur in Fe‐hydroxides and accumulates on the decomposed primary Au‐bearing tellurides such as calaverite, krennerite, and sylvanite. K–Ar dating on vein adularia yielded age of mineralization 7.1–6.9 Ma. Mineralization of the deposit is divided into barren massive quartz (stage I), Au–Ag–Te mineralization occurring in quartz‐adularia‐clays banded ore (Stage II), intensive brecciation (Stage III), post‐ore coarse amethyst (Stage IV), carbonate (Stage V), and supergene stages (Stage VI). In the supergene stage various secondary minerals, including rare bilibinskite, bogdanovite, bessmertnovite metallic alloys, secondary gold, and various oxides, formed under intensely oxidized conditions. Despite heavy oxidation of the ores in the deposit, Te and S fugacities are estimated as Stage II tellurides precipitated at the log f Te2 values ?9 and at log fS2 ?13 based on the chemical compositions of hypogene tellurides and sphalerite. Homogenization temperature of fluid inclusions in quartz broadly ranges from 200 to 300°C. Ore texture, fluid inclusions, gangue, and vein mineral assemblages indicate that the Aginskoe deposit is a low‐sulfidation (quartz–adularia–sericite) vein system.  相似文献   
27.
In Kamchatka, Central Koryak, Central Kamchatka and East Kamchatka metallogenic belts are distributed from northwest to southeast. K–Ar age, sulfur isotopic composition of sulfide minerals, and bulk chemical compositions of ores were analyzed for 13 ore deposits including hydrothermal gold‐silver and base metal, in order to elucidate the geological time periods of ore formation, relationship to regional volcanic belts, type of mineralization, and origin of sulfur in sulfides. The dating yielded ore‐forming ages of 41 Ma for the Ametistovoe deposit in the Central Koryak, 17.1 Ma for the Zolotoe deposit and 6.9 Ma for the Aginskoe deposit in the Central Kamchatka, and 7.4 Ma for the Porozhistoe deposit and 5.1 Ma for the Vilyuchinskoe deposit in the East Kamchatka metallogenic belt. The data combined with previous data of ore‐forming ages indicate that the time periods of ore formation in these metallogenic belts become young towards the southeast. The averaged δ34SCDT of sulfides are ?2.8‰ for the Ametistovoe deposit in Central Koryak, ?1.8‰ to +2.0‰ (av. ?0.1‰) for the Zolotoe, Aginskoe, Baranievskoe and Ozernovskoe deposits in Central Kamchatka, and ?0.7 to +3.8‰ (av. +1.7‰) for Bolshe‐Bannoe, Kumroch, Vilyuchinskoe, Bystrinskoe, Asachinskoe, Rodnikovoe, and Mutnovskoe deposits in East Kamchatka. The negative δ34SCDT value from the Ametistovoe deposit in Central Koryak is ascribed to the contamination of 32S‐enriched sedimentary sulfur in the Ukelayat‐Lesnaya River trough of basement rock. Comparison of the sulfur isotope compositions of the mineral deposits shows similarity between the Central Koryak and Magadan metallogenic belts, and East Kamchatka and Kuril Islands belts. The Central Kamchatka belt is intermediate between these two groups in term of sulfur isotopic composition.  相似文献   
28.
Microbes are ubiquitous in groundwater systems, and they play an important role in the redox state of groundwater and especially on the fate of organic contaminants. In this context, numerical simulations that couple microbial processes to reactive transport models are becoming more popular. In the present work, we revisit the mathematical ground of microbial redox reactions and perform a benchmark analysis of the simulation of aerobic benzene degradation in a shallow and oxidizing aquifer. Numerical results indicate that the two codes tested (one using the finite elements approach and the other using the finite differences approach) lead to very similar results. In addition, the coupling of heterogeneous geochemical reactions to the benchmarked example problem provides a solid basis for the understanding of the redox reactions and the changes on the carbon system triggered by the aerobic degradation of benzene.  相似文献   
29.
新疆乌恰县乌拉根铅锌矿床地质特征和S-Pb同位素组成   总被引:5,自引:0,他引:5  
乌拉根矿床是喀什中新生界凹陷内新近勘查的具超大型远景的铅锌矿床。铅锌矿体呈板状,顺层分布于乌拉根向斜南、北两翼,容矿地层为下白垩统克孜勒苏群第五岩性段(K1kz5)褪色灰白色砂砾岩及古新统阿尔塔什组(E1a)泥质白云岩。矿石具块状、微细浸染状、细脉状、团斑状等构造及胶结结构、交代反映边结构等。乌拉根矿床硫化物δ34S值为-27.9‰~14.6‰,指示相邻层位中石膏、天青石等硫酸盐提供硫,同时有机物的热分解也可能作为硫的来源,硫的还原可能包括生物还原与有机质热化学还原两种模式。硫化物的206Pb/204Pb、207Pb/204Pb、208Pb/204Pb分别为18.528~18.663、15.611~15.669、38.616~38.839,极为均一,指示上地壳和造山带剥蚀区是成矿金属的来源。综合分析乌拉根铅锌矿床地质、地球化学特征,并与已有成因认识进行对比,判定乌拉根矿床是与盆地流体活动相关的砂岩型铅锌矿床。  相似文献   
30.
This paper proposes a method for forecasting the ionospheric critical frequency, f0F2, 1 h in advance, using the support vector machine (SVM) approach. The inputs to the SVM network are the time of day, seasonal information, 2 month running mean sunspot number (R2), 3 day running mean of the 3 h planetary magnetic ap index, the solar zenith angle, the present value f0F2(t) and its first and second increments, the observation of f0F2 at t?23 h, the 30-day mean value at time, t, fmF2 (t) and the previous 30 day running mean of f0F2 at t?23 h fmF2(t?23). The output is the predicted f0F2 1 h ahead. The network is trained to use the ionospheric sounding data at Haikou, Guangzhou, Chongqing, Lanzhou, Beijing, Changchun and Manzhouli stations at high and low solar activities. The performance of the SVM model was verified with observed data. It is shown that the predicted f0F2 has good agreement with the observed f0F2. The performance of the SVM model is superior to that of the autocorrelation and persistence models, and that it is comparable to that of the neural network model.  相似文献   
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