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31.
Lake Sapanca in NW Turkey is a fault originated freshwater basin fed by seasonally variable flows of 15 streams. Considerations of lake–river interaction, supported by statistical measures of 47 bottom samples, suggest that sediment transport and deposition within the lake is controlled by two types of human constructed structures in addition to natural factors: (1) the dykes constructed in the front of streams, which feed the lake by strong flows, to prevent the filling of lakebed by coarse-grained sediments; (2) the constructed regulator on the outflowing Çarksuyu stream results in a higher sedimentation rate of clay-sized material on the NE corner of the lake, which is extraordinary in the shelf environment. 相似文献
32.
M. M. Jordán S. Pina F. García-Orenes M. B. Almendro-Candel E. García-Sánchez 《Environmental Geology》2008,55(2):453-462
The ecologic restoration criteria in areas degraded from extraction activities require making use of their mine spoils. These
materials do not meet fertility conditions to guarantee restoration success and therefore, need the incorporation of organic
amendments to obtain efficient substratum. Reducing the deficiencies in the organic material and restoration material nutrients
with the contribution of treated sewage sludge is proposed in this work. This experiment was based on a controlled study using
columns. The work was conducted with two mine spoils, both very rich in calcium carbonate. The first mineral, of poor quality,
came from the formation of aggregates of crushed limestone (Z). The other residual material examined originated in limestone extraction, formed by the levels of interspersed non-limestone
materials and the remains of stripped soils (D). Two treatments were undertaken (30,000 and 90,000 kg/ha of sewage sludge), in addition to a control treatment. The water
contribution was carried out with a device that simulated either short-duration rain or a flooding irrigation system in order
to cover the surface and then percolate through the soil. The collection of leached water took place 24 h after the applications.
Different parameters of the leached water were determined, including pH, electrical conductivity, nitrate anions, ammonium,
phosphates, sulphates and chlorides. The values obtained for each irrigation application are discussed, and the nitrate values
obtained were very elevated. 相似文献
33.
34.
Jürgen Konzett Daniel J. Frost Alexander Proyer Peter Ulmer 《Contributions to Mineralogy and Petrology》2008,155(2):215-228
Experiments have been conducted in the P-T range 2.5–15 GPa and 850–1,500°C using bulk compositions in the systems SiO2–TiO2–Al2O3–Fe2O3–FeO–MnO–MgO–CaO–Na2O–K2O–P2O5 and SiO2–TiO2–Al2O3–MgO–CaO–Na2O to investigate the Ca-Eskola (CaEs Ca0.5□0.5AlSi2O6) content of clinopyroxene in eclogitic assemblages containing garnet + clinopyroxene + SiO2 ± TiO2 ± kyanite as a function of P, T, and bulk composition. The results show that CaEsss in clinopyroxene increases with increasing T and is strongly bulk composition dependent whereby high CaEs-contents are favoured by bulk compositions with high normative
anorthite and low diopside contents. In this study, a maximum of 18 mol% CaEsss was found at 6 GPa and 1,350°C in a kyanite-eclogite assemblage garnet + clinopyroxene + kyanite + rutile + coesite. By comparison,
no significant increase in CaEsss with increasing P could be observed. If the formation of oriented SiO2-rods frequently observed in eclogititc clinopyroxenes is due to the retrogressive breakdown of a CaEs-component then these
textures are a cooling rather than a decompression phenomenon and are most likely to be found in kyanite-bearing eclogites
cooled from temperatures ≥750°C. The presence of clinopyroxene with approx. 4 mol% CaEsss in an experiment conducted at 2.5 GPa/850°C confirms earlier suggestions based on field data that vacancy-rich clinopyroxenes
are not necessarily restricted to ultrahigh pressure metamorphic conditions.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
35.
Zoltán Zajacz Werner E. Halter Marcel Guillong 《Geochimica et cosmochimica acta》2008,72(8):2169-2197
Analyses of co-existing silicate melt and fluid inclusions, entrapped in quartz crystals in volatile saturated magmatic systems, allowed direct quantitative determination of fluid/melt partition coefficients. Investigations of various granitic systems (peralkaline to peraluminous in composition, log fO2 = NNO−1.7 to NNO+4.5) exsolving fluids with various chlorinities (1-14 mol/kg) allowed us to assess the effect of these variables on the fluid/melt partition coefficients (D). Partition coefficients for Pb, Zn, Ag and Fe show a nearly linear increase with the chlorinity of these fluid (DPb ∼ 6 ∗ mCl, DZn ∼ 8 ∗ mCl, DAg ∼ 4 ∗ mCl, DFe ∼ 1.4 ∗ mCl, where mCl is the molinity of Cl). This suggests that these metals are dissolved primarily as Cl-complexes and neither oxygen fugacity nor the composition of the melt affects significantly their fluid/melt partitioning. By contrast, partition coefficients for Mo, B, As, Sb and Bi are highest in low salinity (1-2 mol/kg Cl) fluids with maximum values of DMo ∼ 20, DB ∼ 15, DAs ∼ 13, DSb ∼ 8, DBi ∼ 15 indicating dissolution as non-chloride (e.g., hydroxy) complexes. Fluid/melt partition coefficients of copper are highly variable, but highest between vapor like fluids and silicate melt (DCu ? 2700), indicating an important role for ligands other than Cl. Partition coefficients for W generally increase with increasing chlorinity, but are exceptionally low in some of the studied brines which may indicate an effect of other parameters. Fluid/melt partition coefficients of Sn show a high variability but likely increase with the chlorinity of the fluid (DSn = 0.3-42, DW = 0.8-60), and decrease with decreasing oxygen fugacity or melt peraluminosity. 相似文献
36.
Luis A. Spalletti Ignasi Queralt Sergio D. Matheos Ferrn Colombo Jorge Maggi 《Journal of South American Earth Sciences》2008,25(4):440-463
The Upper Jurassic Tordillo Formation is exposed along the western edge of the Neuquén Basin (west central Argentina) and consists of fluvial strata deposited under arid/semiarid conditions. The pebble composition of conglomerates, mineralogical composition of sandstones and pelitic rocks, and major- and trace-element geochemistry of sandstones, mudstones, and primary pyroclastic deposits are evaluated to determine the provenance and tectonic setting of the sedimentary basin. Conglomerates and sandstones derived almost exclusively from volcanic sources. The stratigraphic sections to the south show a clast population of conglomerates dominated by silicic volcanic fragments and a predominance of feldspathic litharenites. This framework composition records erosion of Triassic–Jurassic synrift volcaniclastic rocks and basement rocks from the Huincul arch, which was exhumed as a result of Late Jurassic inversion. In the northwestern part of the study area, conglomerates show a large proportion of mafic and acidic volcanic rock fragments, and sandstones are characterised by a high content of mafic volcanic rock fragments and plagioclase. These data suggest that the source of the sandstones and conglomerates was primarily the Andean magmatic arc, located west of the Neuquén Basin. The clay mineral assemblage is interpreted as the result of a complex set of factors, including source rock, climate, transport, and diagenesis. Postdepositional processes produced significant variations in the original compositions, especially the fine-grained deposits. The Tordillo sediments are characterised by moderate SiO2 contents, variable abundances of K2O and Na2O, and a relatively high proportion of ferromagnesian elements. The degree of chemical weathering in the source area, expressed as the chemical index of alteration, is low to moderate. The major element geochemistry and Th/Sc, K/Rb, Co/Th, La/Sc, and Cr/Th values point to a significant input of detrital volcanic material of calcalkaline felsic and intermediate composition. However, major element geochemistry is not useful for interpreting the tectonic setting. Discrimination plots based on immobile trace elements, such as Ti, Zr, La, Sc, and Th, show that most data lie in the active continental margin field. Geochemical information is not sufficiently sensitive to differentiate the two different source areas recognized by petrographic and modal analyses of conglomerates and sandstones. 相似文献
37.
The passivation of calcite by acid mine water. Column experiments with ferric sulfate and ferric chloride solutions at pH 2 总被引:2,自引:1,他引:1
Josep M. Soler Marco Boi Jos Luis Mogolln Jordi Cama Carlos Ayora Peter S. Nico Nobumichi Tamura Martin Kunz 《Applied Geochemistry》2008,23(12):3579-3588
Column experiments, simulating the behavior of passive treatment systems for acid mine drainage, have been performed. Acid solutions (HCl or H2SO4, pH 2), with initial concentrations of Fe(III) ranging from 250 to 1500 mg L−1, were injected into column reactors packed with calcite grains at a constant flow rate. The composition of the solutions was monitored during the experiments. At the end of the experiments (passivation of the columns), the composition and structure of the solids were measured. The dissolution of calcite in the columns caused an increase in pH and the release of Ca into the solution, leading to the precipitation of gypsum and Fe–oxyhydroxysulfates (Fe(III)–SO4–H+ solutions) or Fe–oxyhydroxychlorides (Fe(III)–Cl–H+ solutions). The columns worked as an efficient barrier for some time, increasing the pH of the circulating solutions from 2 to 6–7 and removing its metal content. However, after some time (several weeks, depending on the conditions), the columns became chemically inert. The results showed that passivation time increased with decreasing anion and metal content of the solutions. Gypsum was the phase responsible for the passivation of calcite in the experiments with Fe(III)–SO4–H+ solutions. Schwertmannite and goethite appeared as the Fe(III) secondary phases in those experiments. Akaganeite was the phase responsible for the passivation of the system in the experiments with Fe(III)–Cl–H+ solutions. 相似文献
38.
39.
National flood discharge mapping in Austria 总被引:5,自引:0,他引:5
This article presents the approach and the results of a study in which 30, 100 and 200 year return period flood discharges
were estimated for 26,000 km of Austrian streams. Three guiding principles were adopted: combination of automatic methods
and manual assessments by hydrologists to allow speedy processing and account for the local hydrological situation; combination
of various sources of information including flood peak samples, rainfall data, runoff coefficients and historical flood data;
and involvement of the Hydrographic Services to increase the accuracy and enhance the acceptance of results. The flood discharges
for ungauged catchments were estimated by the Top-kriging approach with manual adjustment to the local flood characteristics.
The adopted combination approach proved to be very efficient both in terms of the project time required and in terms of the
accuracy and acceptability of the estimated flood discharges of given return periods. 相似文献
40.
B. Bühn 《Mineralogy and Petrology》2008,92(3-4):453-470
Summary Two bimodal carbonatite complexes in Namibia of Cretaceous age are explored as to the presence and composition of a coexisting
carbonatitic fluid. The Kalkfeld and Ondurakorume complexes contain both Ca- and Mg/Fe-carbonatites, composed of calcite alone
or calcite with ferroan dolomite, fluorapatite and strontianite. The major element evolution in the bulk rocks from s?vites
to beforsites is due to crystallization of calcite and fluorapatite. All carbonatites show a negative Y anomaly in normalised
REE plots. Fractionation is accompanied by successively lower HREE contents between Tb and Yb, expressed by the ratios Nd/Ho
and Ho/Lu. The evolution of this downward-facing hump goes along with decreasing Y contents in bulk rocks and minerals. All
this requires an additional phase coexisting with the carbonate liquid during fractionation. Comparison between the bulk rocks
and the expelled fluid shows that the latter had preferentially accumulated the HREE and Y. Further evidence for this process
are hydrothermal, HREE, Y-rich fluorites in other carbonatite complexes which reflect the composition of the expelled fluid.
The high strength of fluoride complexes suggests that fluoride complexing in the carbonatitic fluid is the process responsible
for extracting HREE and Y from the carbonatite magma, leaving fractionated carbonatite rocks depleted in these elements. The
geochemical evolution of carbonatite magmas along fractionation has therefore to be considered in a melt-mineral-fluid system.
Correspondence: B. Bühn, Instituto de Geociências, Universidade de Brasilia, Campus Universitário Darcy Ribeiro, Brasilia
70910-900, Brazil 相似文献