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21.
The Mössbauer fractions f for various ferrous- and/or ferric-containing oxides and oxyhydroxides, silicates and carbonates were evaluated from the experimental temperature dependence of their center shifts, using the Debye approximation for the second-order Doppler shift. It is concluded that ferrous ions exhibit a lower fraction as compared to ferric ions. Using standard mixtures of -Fe2O3 with selected Fe2+ or Fe3+ compounds, it is found that the calculated Fe3+
f values are somewhat overestimated with respect to those of Fe2+. Possible explanations for this shortcoming are discussed and it is suggested that a different temperature dependence of the intrinsic isomer shift is the most likely reason. This suggestion is corroborated by analyses of hematite and hedenbergite data which are available for temperatures up to 900 K and 800 K respectively. 相似文献
22.
Plant pigment decay constants were determined for four macrophytes collected from the Hudson Estuary.Typha angustifolia andScirpus fluviatilis were used as representatives of emergent aquatic vegetation (EAV), andPotamogeton sp. andVallisneria americana were used to represent submerged aquatic vegetation (SAV). Litter bags were maintained in an environmental chamber in the dark for 104 d. The fastest rate of total mass loss was in the SAVV. americana and slowest in the EAVT. angustifolia. Changes in carotenoid and chloropigment concentration resulting from microbial and meiofaunal heterotrophy in each of the macrophytes were quantified using reverse-phase, high-performance liquid chromatography (RP-HPLC) techniques. Chlorophyllc and the carotenoid, fucoxanthin, provided useful biomarkers in determining the presence of epiphytic diatom growth, which only occurred on the SAV. The highest concentrations of phaeophorbidea, commonly used as an indication of metazoan grazing, were found in the SAVV. americana. Low concentrations of phaeophorbidea in the SAVPotamogeton sp. indicate inefficient use of this SAV by meiofaunal grazers. Lutein decayed slower than all other carotenoids in both EAV and SAV. Microcosm studies such as this are necessary to further understand the mechanisms and kinetics of photosynthetic pigment transformations in natural systems. 相似文献
23.
For the period August 1959–December 1964 the Greenwich Photoheliographic Results were searched for sunspot nests. Such a nest is a sequence of sunspot groups that appear within a small area on the solar surface and that last for several months. The search procedure is described and data for 41 probable sunspot nests are given. At least three quarters of these nests appear to be real, and not chance clusters.The nests are the same type of activity sequences as the Fleckenherde discovered by Becker (1955) and the complexes of activity pointed out by Gaizauskas et al. (1983). The complexes of activity as defined by Bumba and Howard (1965) are different patterns, however; the relation between complexes and the nests is shown.Some properties of the nests are: (i) many nests appear as double structures; (ii) single nests and components of double nests are quite compact: the effective areas are comparable to those of medium-large sunspot groups; (iii) each nest rotates at its own steady rate about the Sun; (iv) the intrinsic scatter in the rotation rates is much larger than the trend in the differential rotation; (v) displacements in latitude are less than a few meters per second; (vi) many nests live for 6 to 15 Carrington rotation periods, the minimum lifetime is not yet determined; (vii) the fraction of the sunspot groups that are members of nests is large (at least 30%). 相似文献
24.
Absolute masses for W Ursae Majoris and Algol-type close binaries can be determined from their parallax, if observed, and the relative sizes of the stars and their mass ratio, obtained from a light curve solution. An error propagation study compares the typical order of magnitude of the various terms involved, and shows how accurate parallaxes have to be in order to make the procedure work, i.e., making the parallax term not larger than the combined non-parallax terms, and producing reasonably low mass errors. Some comments are made on the possibilities with respect to the HIPPARCOS program.Communication presented at the International Conference on Astrometric Binaries, held on 13–15 June, 1984, at the Remeis-Sternwarte Bamberg, Germany, to commemorate the 200th anniversary of the birth of Friedrich Wilhelm Bessel (1784–1846). 相似文献
25.
On the coronograph spectrophotographic records taken on 31.372 UT, August 1979, some faint emission features were found which can be ascribed to Siii and Niii. These emissions were obviously a transient phenomena which were detected only 10 hr after the supposed fall of Comet 1979 XI in the Sun's photosphere. It cannot be excluded that the appearance of Si and Ni lines was triggered by the evaporation of dust particles with a high abundance of heavier elements in the solar corona. This assumption is also supported by intensity distribution of the Fex coronal line around the Sun's limb. The maximum coincide with the position angle of the projected path of the comet. 相似文献
26.
Combined fluid inclusion microthermometry and microanalysis by laser ablation inductively coupled plasma mass spectrometry
(LA-ICPMS) are used to constrain the hydrothermal processes forming a typical Climax-type porphyry Mo deposit. Molybdenum
mineralisation at Questa occurred in two superimposed hydrothermal stages, a magmatic-hydrothermal breccia and later stockwork
veining. In both stages, texturally earliest fluids were single-phase, of low salinity (~7 wt.% NaClequiv.) and intermediate-density. Upon decompression to ~300 bar, they boiled off a vapour phase, leaving behind a residual brine
(up to 45 wt.% NaClequiv) at temperatures of ~420°C. The highest average Mo concentrations in this hot brine were ~500 μg/g, exceeding the Mo content
of the intermediate-density input fluid by about an order of magnitude and reflecting pre-concentration of Mo by fluid phase
separation prior to MoS2 deposition from the brine. Molybdenum concentrations in brine inclusions, then, decrease down to 5 μg/g, recording Mo precipitation
in response to cooling of the saline liquid to ~360°C. Molybdenite precipitation from a dense, residual and probably sulphide-depleted
brine is proposed to explain the tabular shape of the ore body and the absence of Cu-Fe sulphides in contrast to the more
common Cu-Mo deposits related to porphyry stocks. Cesium and Rb concentrations in the single-phase fluids of the breccia range
from 2 to 8 and from 40 to 65 μg/g, respectively. In the stockwork veins, Cs and Rb concentrations are significantly higher
(45–90 and 110–230 μg/g, respectively). Because Cs and Rb are incompatible and hydrothermally non-reactive elements, the systematic
increase in their concentration requires two distinct pulses of fluid exsolution from a progressively more fractionated magma.
By contrast, major element and ore metal concentrations of these two fluid pulses remain essentially constant. Mass balance
calculations using fluid chemical data from LA-ICPMS suggest that at least 25 km3 of melt and 7 Gt of deep input fluid were necessary to provide the amount of Mo contained in the stockwork vein stage alone.
While the absolute amounts of fluid and melt are uncertain, the well-constrained element ratios in the fluids together with
empirical fluid/melt partition coefficients derived from the inclusion analyses suggest a high water content of the source
melt of ~10%. In line with other circumstantial evidence, these results suggest that initial fluid exsolution may have occurred
at a confining pressure exceeding 5 kbar. The source of the molybdenum-mineralising fluids probably was a particularly large
magma chamber that crystallised and fractionated in the lower crust or at mid-crustal level, well below the shallow intrusions
immediately underlying Questa and other porphyry molybdenum deposits.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
27.
Thomas B. Boving Mark H. Stolt Janelle Augenstern Brian Brosnan 《Environmental Geology》2008,55(3):571-582
The control of polluted surface runoff and the assessment of possible impacts on groundwater is a concern at the local and
regional scale. On this background, a study investigates possible impacts of organic and inorganic pollutants (including bacteria)
originating from a permeable asphalt parking lot on the water quality immediately beneath it. The functioning of the permeable
pavement, including clogging and restricted vertical percolation, was also evaluated. Four nested sample ports (shallow and
deep) were installed below low- and high-traffic areas, including one port outside the parking lot. At least initially there
was a good hydraulic connection between the parking surface and the shallow sample ports. The presence of a geotextile layer
at the base of the parking lot structure, however, was identified in lab tests as one factor restricting vertical percolation
to the deeper ports. Clogging of the permeable surface was most pronounced in heavy traffic areas and below snow pile storage
areas. Corroborated by high electric conductivity and chloride measurements, sand brought in by cars during winter was the
principal cause for clogging. No bacteria or BOD were found in percolating water. Polycyclic aromatic hydrocarbons (PAH) were
present at concentrations near minimum detection limit. Nutrients (nitrate and phosphate) were being leached into the ground
via the permeable parking lot surface at annual flux rates of 0.45–0.84 g/m2/year. A multi-species tracer test demonstrated a retention capacity of the permeable parking lot structure of >90% for metals
and 27% for nutrients, respectively. 相似文献
28.
Helmut Kerndorff Stephan Kühn Thomas Minden Dagmar Orlikowski Thomas Struppe 《Environmental Geology》2008,55(2):291-301
The aim of this research project is to identify, characterize and quantify natural attenuation (NA) processes in groundwater
affected by emissions of abandoned waste disposal sites in Berlin-Kladow/Gatow, Germany. It is part of the funding priority
called KORA established by the Federal Ministry for Education and Research (BMBF) to explore the extent to which NA can be
used for remedial purposes for varied forms of soil and groundwater contamination. Information on the emission behaviour of
individual parameters is generated on the basis of hydrogeochemical comparison of 20 years old and new data. Using groundwater-modelling
and CFC-analysis, information on the transport and retention of pollutants in groundwater is compiled. The microbial colonization
of contaminated aquifers is characterized by molecular biological methods [polymerase chain reaction (PCR) and denaturing
gradient gel electrophoresis (DGGE)] to differentiate between contaminated and not contaminated zones. 相似文献
29.
V. B. Naumov V. S. Kamenetsky R. Thomas N. N. Kononkova B. N. Ryzhenko 《Geochemistry International》2008,46(6):554-564
Melt inclusions were studied in chrome diopside from the Inagli deposit of gemstones in the Inagli massif of alkaline ultrabasic rocks of potassic affinity in the northwestern Aldan shield, Yakutia, Russia. The chrome diopside is highly transparent and has an intense green color. Its Cr2O3 content varies from 0.13 to 0.75 wt %. Primary and primary-secondary polyphase inclusions in chrome diopside are dominated by crystal phases (80–90 vol %) and contain aqueous solution and a gas phase. Using electron microprobe analysis and Raman spectroscopy, the following crystalline phases were identified. Silicate minerals are represented by potassium feldspar, pectolite [NaCa2Si3O8(OH)], and phlogopite. The most abundant minerals in the majority of inclusions are sulfates: glaserite (aphthitalite) [K3Na(SO4)2], glauberite [Na2Ca(SO4)2], aluminum sulfate, anhydrite (CaSO4), gypsum (CaSO4 × 2H2O), barite (BaSO4), bloedite [Na2Mg(SO4)2 × 4H2O], thenardite (NaSO4), polyhalite [K2Ca2Mg(SO4)4 × 2H2O], arcanite (K2SO4), and celestite (SrSO4). In addition, apatite was detected in some inclusions. Chlorides are probably present among small crystalline phases, because some analyses of aggregates of silicate and sulfate minerals showed up to 0.19–10.3 wt % Cl. Hydrogen was identified in the gas phase of polyphase inclusions by Raman spectroscopy. The composition of melt from which the chrome diopside crystallized was calculated on the basis of the investigation of silicate melt inclusions. This melt contains 53.5 wt % SiO2, considerable amounts of CaO (16.3 wt %), K2O (7.9 wt %), Na2O (3.5 wt %), and SO3 (1.4 wt %) and moderate amounts of Al2O3 (7.5 wt %), MgO (5.8 wt %), FeO (1.1 wt %), and H2O (0.75 wt %). The content of Cr2O3 in the melt was 0.13 wt %. Many inclusions were homogenized at 770–850°C, when all of the crystals and the gas phase were dissolved. The material of inclusions heated up to the homogenization temperature became heterogeneous even during very fast quenching (two seconds) producing numerous small crystals. This fact implies that most of the inclusions contained a salt (rather than silicate) melt of sulfate-dominated composition. Such inclusions were formed from salt globules (with a density of about 2.5 g/cm3) occurring as an emulsion in the denser (2.6 g/cm3) silicate melt from which the chrome diopside crystallized. 相似文献
30.
The current study provides an investigation of abiotic reduction of an oversaturated uranyl solution driven by iron nanoparticle oxidation. The reactivity of nano-scale zero-valent iron (ZVI) under mildly oxic conditions (1.2% O2 and 0.0017% CO2) was studied in 1000 ppm uranyl solution in the pH range 3-7, at reaction times from 10 min to 4 h. Reductive precipitation of UO2 was observed as the main process responsible for the removal of uranium from solution with the kinetics of reaction becoming increasingly favourable at higher pH. Despite working with an oversaturated uranium solution, the precipitation of UO2 occurred in preference to precipitation of UO3·2H2O (metaschoepite) at reaction times between 1 and 4 h and for uranyl solutions initially set up at pH ?5. Characterisation of both solid and solution phases was performed using X-ray photoelectron spectroscopy (XPS), focused ion beam (FIB) imaging, X-ray diffraction (XRD) and inductively coupled plasma atomic emission spectroscopy (ICP-AES). 相似文献