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1.
M Grande R BrowningN Waltham D ParkerS.K Dunkin B KentB Kellett C.H PerryB Swinyard A PerryJ Feraday C HoweG McBride K PhillipsJ Huovelin P MuhliP.J Hakala O VilhuJ Laukkanen N ThomasD Hughes H AlleyneM Grady R LundinS Barabash D BakerP.E Clark C.D MurrayJ Guest I CasanovaL.C d'Uston S MauriceB Foing D.J Heather V FernandesK Muinonen S.S RussellA Christou C OwenP Charles H KoskinenM Kato K SipilaS Nenonen M HolmstromN Bhandari R ElphicD Lawrence 《Planetary and Space Science》2003,51(6):427-433
The D-CIXS Compact X-ray Spectrometer will provide high quality spectroscopic mapping of the Moon, the primary science target of the ESA SMART-1 mission. D-CIXS consists of a high throughput spectrometer, which will perform spatially localised X-ray fluorescence spectroscopy. It will also carry a solar monitor, to provide the direct calibration needed to produce a global map of absolute lunar elemental abundances, the first time this has been done. Thus it will achieve ground breaking science within a resource envelope far smaller than previously thought possible for this type of instrument, by exploiting two new technologies, swept charge devices and micro-structure collimators. The new technology does not require cold running, with its associated overheads to the spacecraft. At the same time it will demonstrate a radically novel approach to building a type of instrument essential for the BepiColombo mission and potential future planetary science targets. 相似文献
2.
The diffusion in a shearing oscillatory flow from an instantaneous surface point source is considered. An analytical solution
is obtained by Fourier transform. The results show that, for three dimensional diffusion in an oscillatory flow with constant
shear, the distribution of the contaminant follows the multivariate Gaussian distribution rule. When the frequency is very
high, or the time very short, the shear does not influence the diffusion. For moderate values of time, there are fluctuations
with longitudinal variance. For large values of time the longitudinal variance increases as t, and the peak concentration
decreases as t−1.5, which are faster than those in a flow without shear, but much slower than those in a steady flow, where the longitudinal
variance increases as t3 and the peak concentration decreases as t−2.5. The contaminant patch is elongated in the longitudinal direction of the shear flow and moves back and forth with the water
motion.
Contribution No. 1306 from the Institute of Oceanology, Academia Sinica. Received July 12, 1985 相似文献
3.
4.
Roberto F. Viotti Rosario González-Riestra Takashi Iijima Stefano Bernabei Riccardo Claudi Jochen Greiner Michael Friedjung Vito Francesco Polcaro Corinne Rossi 《Astrophysics and Space Science》2005,296(1-4):435-439
We review the main characteristics of the symbiotic system AG Draconis, with special emphasis on its optical and X-ray variations.
We also discuss the X-ray to visual energy distribution during quiescence and outburst and describe our spectroscopic and
X-ray observations during the 2003 outburst.
Based on X-ray observations collected with the XMM–Newton Observatory, on INES data from the IUE satellite, and on optical
spectra collected with the Asiago–Cima Ekar, Bologna–Loiano and La Palma–Galileo Italian telescopes. 相似文献
5.
6.
Dr. M. Shimizu Dr. C. J. Stanley Dr. A. J. Criddle Dr. A. Kato Dr. S. Matsubara 《Mineralogy and Petrology》1991,45(1):11-17
Summary New compositional and optical data are reported for antimonian and antimonianbismuthian varieties of hemusite from epithermal Au-Ag-Cu deposits in Japan. The empirical formula for the antimonian variety, from the Iriki mine is: (Cu5.83Fe0.14Ag0.01)5.98Mo1.03(Sn0.54Sb0.41Te0.03Bi0.02)1.00(S7.85Se0.15)8.00, and that of the Sb-Bi variety from the Kawazu mine is: (Cu5.84Fe0.14Ag0.01)5.99Mo1.03(Sn0.82Sb0.11Bi0.l0Te0.04)1.07(S7.80Se0.12)7.92. The theoretical formula of hemusite is Cu+
4Cu2+
2MO4+Sn4+S8, whilst the most probable formula of the Iriki hemusite is Cu+
4.5CU2+
1.5Mo4+Sn4+
0.5Sb5+
0.5S8, with Sb5+ substituting for Sn4+ and forming (SbS4)3– tetrahedra as might be expected, given that the metal to sulphur ratio is 1, and given the sphalerite-like structure of the mineral. However Bi3+ cannot be so accommodated, resulting in a deficiency in (S + Se) for Kawazu hemusite. Reflectance spectra for both are compared with those of the tungsten analogue (compositional) of hemusite, kiddcreekite. The relationship between hemusitesensu stricto and these newly reported varieties is discussed in terms of simple and coupled chemical substitutions, and inferences are drawn on the valency of Sb, Bi, Mo and Cu in the hemusite structure.
Neue chemische und optische Daten für antimon- und bismuthführende Varietäten von Hemusit aus Japan
Zusammenfassung Neue chemische und optische Daten für antimon- und bismuthführende Hemusite auf epithermalen Au-Ag-Cu Lagerstätten in Japan werden vorgelegt. Die empirische Formel für die antimon-führende Varietät aus der Iriki-Mine ist: (Cu5.83Fe0.14Ag0.01)5.98Mo1.03(Sn0.54Sb0.41Te0.03Bi0.02)1.00 (S7.85Se0.15)8.00, und die der Sb-Bi Varietät aus der Kawazu Mine ist: (Cu5.84Fe0.14Ag0.01)5.99M01.03(Sn0.82Sb0.11Bi0.l0Te0.04)1.07 (S7.80Se0.12)7.92. Die theoretische Formel von Hemusit ist Cu+ 4Cu2+ 2Mo4+Sn4+S8, während die wahrscheinlichere Formel für den Hemusit von Iriki Cu+ 4Cu2+ 1.5Mo4+Sn4+ 0.5Sb5+ 0.5S8, mit Sb5+ an der Stelle von Sn4+, das(SbS4)3– Tetraeder bildet, wie zu erwarten ist, unter der Voraussetzung, da das Metall zu Schwefelverhältnis 1 und die Struktur sphaleritähnlich ist. Bi3+ kann jedoch nicht in dieser Weise untergebracht werden, und das führt zu einem Mangel an (S + Se) für den Hemusit von Kawazu. Die Reflektions-Spektren beider Minerale werden mit denen des Wolfram-Equivalents von Hemusit (Kiddcreekit) verglichen. Die Beziehung zwischen Hemusitsensu stricto und diesen jetzt beschriebenen Varietäten wird auf der Basis einfacher und gekoppelter chemischer Substitution diskutiert. Auf dieser Basis werden Schlüsse auf die Valenz von Sb, Bi Mo und Cu in der Hemusit-Struktur gezogen.相似文献
7.
Yusuke Seto Naoya Sakamoto Takashi Kaito Hisayoshi Yurimoto 《Geochimica et cosmochimica acta》2008,72(11):2723-2734
We report the mineral compositions and micro-texture of the isotopically anomalous (δ17,18OSMOW ∼ +180‰) Fe-S-Ni-O material recently discovered in matrix of the primitive carbonaceous chondrite Acfer 094 [Sakamoto N., Seto Y., Itoh S., Kuramoto K., Fujino K., Nagashima K., Krot A. N. and Yurimoto H. (2007) Oxygen isotope evidence for remnants of the early solar system primordial water. Science317, 231-233]. Synchrotron radiation X-ray diffraction and transmission electron microscopy studies indicate that this material consists of the symplectitically intergrown magnetite (Fe3O4) and pentlandite (Fe5.7Ni3.3S8) with magnetite/pentlandite volume ratio of ∼2.3. Magnetite forms column-shaped grains (10-30 nm in diameter and 100-200 nm in length); pentlandite occurs as worm-shaped grains or aggregates of grains 100-300 nm in size between magnetite crystals. Although both the X-ray diffraction and electron energy loss spectra support identification of iron oxide as magnetite, the electron diffraction patterns show that magnetite has a weak 3-fold superstructure, possibly due to ordering of vacancies. We infer that the isotopically anomalous symplectite formed by sulfurization and oxidization of metal grains either in the solar nebula or on an icy planetesimal. The intersite cation distribution of pentlandite suggests that timescale of oxidation was no longer than 1000 years. 相似文献
8.
Toru?Iwata Keiko?Yoshikawa Katsutoshi?Nishimura Yoshihisa?Higuchi Takao?Yamashita Shigeru?Kato Eiji?OhtakiEmail author 《Journal of Oceanography》2004,60(6):995-1000
The measurements of the vertical transport of CO2 were carried out over the Sea of Japan using the specially designed pier of Kyoto University on September 20 to 22, 2000. CO2 fluxes were measured by the eddy correlation and aerodynamic techniques. Both techniques showed comparable CO2 fluxes during sea breeze conditions: −0.001 to −0.08 mg m−2s−1 with the mean of −0.05 mg m−2s−1. This means that the measuring site satisfies the fetch requirement for meteorological observations under sea breeze conditions. Moreover, the eddy diffusivity coefficient used in the aerodynamic technique is found to be consistent with the coefficient used in the eddy correlation technique. The present result leads us to conclude that the aerodynamic technique may be applicable to underway CO2 flux measurements over the ocean and may be used in place of the bulk technique. The important point is the need to maintain a measuring accuracy of CO2 concentration difference of the order of 0.1 ppmv on the research vessels or the buoys. 相似文献
9.
Decadal variability of subsurface temperature in the North Pacific has been investigated. Two dominant regions were found;
the central subarctic region (CSa) and the north-eastern subtropical region (NESt). In CSa, cooling (warming) of wintertime
subsurface temperature corresponds to the large (small) temperature gradient and southward (northward) shift of subsurface
temperature front, associated with the increase (decrease) of positive wind stress curl and the southward (northward) shift
of curl τ zero line with 2 years delay. It is suggested that the relocation of subtropical-subarctic boundary plays an important
role. In NESt, importance of heat flux through the sea surface and heat divergence in the Ekman layer is also discussed.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
10.
The presence of organic ligands (L) whose conditional stability constants (KML) are strong enough to allow them to form complexes with copper has been reported in oceanic waters. However, there is no general agreement on the distributional characteristics of such strong ligands in the water column. We present that these inconsistencies are derived from not only different analytical methods employed for their detection but also different oceanographic conditions. In particular, the nature and quantities of detectable natural ligands are affected by what kind of form the ligands are presentin situ in different marine environments, that is, chemical speciation of natural ligands (ligand speciation), which depends strongly on the variations in concentrations of coexisting trace metals. Using published data from observations in the laboratory and the field, we provide limits to the ranges of conditional stability constants of organic ligands for copper, zinc and cadmium that are detectable by the extensively used direct metal-titration method. For example, our model indicates that organic ligands for copper with log KCuL(Cu)>12.4 in surface water and with log KCuL(Cu)>9.9 in deep water might not have been detected because stronger ligands had formed complexes with ambient metalsin situ at a station in the North Pacific. The estimation suggests that there is a basinscale difference in speciation of natural organic ligands and, moreover, that this difference influences metal speciation. It is postulated that comparisons of the occurrence and levels of organic ligands might not be possible among spatially and temporally different observations without reconciliation of the effects of speciation of the ligands, even if an identical method is used in every case. 相似文献