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231.
Spherical aggregates of orthopyroxene are reported from some parts of the Bushveld Complex in a variety of host rocks.Detailed mapping has shown that these spherical aggregates, comprising pyroxenite spheroids in a quartz-norite matrix, are contact phenomena and not stratigraphic markers. Orthopyroxene, biotite and amphibole are enriched in spheroids relative to matrix; their mineral chemistry showing a fairly constant orthopyroxene and plagioclase composition through the spheroids and into the matrix, indicating in-situ formation.Bulk chemistry shows spheroid to matrix tie-lines orthogonal to those generally accepted for silicate liquid immiscibility, but other chemical information is consistent with the occurrence of immiscibility.The formation of the aggregates may be related to the industrial process of spherical agglomeration, by which spheroids are formed by the introduction of an immiscible “bridging liquid” to the melt — probably derived from the floor rocks in this case. The mechanism accounts for the field relationships, petrography and chemistry of the aggregate-matrix system. The petrology of the process equates with a special case of silicate liquid immiscibility induced by local contamination and ageing of the original magma.A similar “bridging liquid” mechanism could also account for the formation of the so-called “boulder bed” beneath the Merensky Reef. 相似文献
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233.
Camille Cordes Larry Atkinson Richard Lee Jack Blanton 《Marine pollution bulletin》1980,11(11):315-317
Following the Ixtoc I oil rig blowout in Campeche Bay we hypothesized that resulting tarballs should eventually appear in the Gulf Stream off Gerogia and that because of dynamic barriers in the innershelf little would reach nearshore areas. To test these hypotheses, surface tows to collect floating tar were taken off the coasts of Georgia and Florida in October and December, 1979.No tar was found within 40 km of the shore. All samples more than 40 km offshore contained some tar. The mean concentration was 0.82 mg m?2 with a range of 0.01–5.6 mg m?2. Closely spaced sampling showed extreme variation but trends were consistent. Perylene was the most abundant compound in the tarballs. 相似文献
234.
W. Bell C. Paton Walsh P.T. Woods T.D. Gardiner M.P. Chipperfield A.M. Lee 《Journal of Atmospheric Chemistry》1998,30(1):131-140
We outline how ground-based Fourier transform infrared (FTIR) measurements of stratospheric trace species, obtained with high temporal resolution, could be used to detect filaments of polar vortex air at mid-latitudes and therefore test high spatial resolution chemical transport models (CTMs). Vertical column abundances of HCl, ClONO2, HNO3, N2O and HF have been obtained from FTIR solar absorption measurements made throughout the day from Aberdeen, UK (57°N, 2°W) on several days during winter/spring 1993/94 and 1994/95. The short-timescale ( 2 hours) variability observed in the columns is attributed to real atmospheric variations and is often associated with the passage of high latitude air over Aberdeen. This is confirmed by 3D modelling studies which qualitatively reproduce and rationalise the observed changes in the column data on January 19 1994, January 20 1995 and February 26 1995. We describe the viewing geometry of ground-based FTIR measurements and we suggest a measurement strategy which should maximise the information retrieved on horizontal gradients in stratospheric trace species columns from FTIR measurements. 相似文献
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236.
Green and Vernon (1974) have experimentally determined a divariant field of cordierite-orthoamphibole-kyanite-quartz with a slope of 12±4 bars per °C occurring between 8.0 and 10.4 kbar at 750° C and between 9.5 and 11.3 kbar at 850° C. However, the writers' thermodynamic calculation of the divariant band indicates a more limited range of 0.65 and 0.7 kbar at 750° C and 850° C respectively, with an estimated error of ±0.2 kbar. 相似文献
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238.
The voltage induced in a horizontal loop on a layered ground has been calculated for the case where the loop is excited by a step current and measurements are made during the off-cycle. The expressions derived for a uniform ground show that for large time t the induced voltage E(t) is approximately given by E(t)?— (Ibαμ/20t) (σμ2/t)3/2 where σ is the conductivity of the ground, μ the permeability, b the loop radius, and I the amplitude of the current step. For small times the corresponding result is E(t)?—Ibμ/2t. When the ground is composed of a number of layers a numerical procedure for calculating the induced voltage is described. The calculated responses of various multilayered structures show that at short times the induced voltage is asymptotic to that produced in the case of a uniform ground of conductivity equal to the top layer. Interference effects in the top layer can lead to anomalous decay curves which may result in the underestimation of the conductivity of a buried layer. 相似文献
239.
240.
Jin‐Jing Lee Cheng‐Shin Jang Sheng‐Wei Wang Chin‐Ping Liang Chen‐Wuing Liu 《水文研究》2008,22(16):3029-3041
This study characterized the redox conditions in arsenic‐affected groundwater aquifers of the Lanyang plain, Taiwan. Discriminant analysis was adopted to delineate three redox zones (oxidative, transitional and reductive zones) in different aquifers and yielded 92·3% correctness on groundwater quality data. Arsenic is mainly distributed in the reductive zone, and arsenic distribution in the shallow aquifer is mainly affected by surface activities. According to PHREEQC modelling results, possible mechanisms for arsenic release to groundwater in Lanyang plain are explored. Arsenic released to groundwater in the oxidative zone (zone 1) is primarily caused by the oxidations of arsenic‐bearing pyrite minerals, and arsenate is the predominant species. While the reductive dissolution of Fe‐oxides are responsible for the high arsenic concentration found in the transitional and reductive zones (zones 2 and 3), arsenite is the predominant species. The reduction potential of groundwater rises as the depths and zones increase. Some sulphates may be reduced to form sulphide ions, which then react with arsenic to form arseno‐sulphide deposits (such as realgar, orpiment) and then slightly lower groundwater arsenic concentrations. A conceptual diagram which summarized the possible release processes of arsenic in different redox zones along groundwater flow in Lanyang plain is postulated. Arsenic‐bearing pyrite and arsenopyrite (FeAsS) are oxidized as they are exposed to the infiltrated oxygenated rainwater, releasing soluble arsenate Fe(II) and SO42? into zone 1. The dissolution of arsenic‐rich Fe‐oxides due to the onset of reducing conditions in zones 2 and 3 is responsible for the mobility of arsenic and likely to be the primary mechanism of arsenic release to groundwater in the Lanyang plain Copyright © 2007 John Wiley & Sons, Ltd. 相似文献