首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   133篇
  免费   3篇
  国内免费   12篇
测绘学   3篇
大气科学   2篇
地球物理   14篇
地质学   77篇
海洋学   7篇
天文学   35篇
综合类   4篇
自然地理   6篇
  2023年   3篇
  2020年   1篇
  2019年   6篇
  2018年   7篇
  2017年   6篇
  2016年   5篇
  2015年   3篇
  2014年   10篇
  2013年   4篇
  2012年   7篇
  2011年   12篇
  2010年   7篇
  2009年   10篇
  2008年   9篇
  2007年   14篇
  2006年   7篇
  2005年   1篇
  2004年   7篇
  2003年   6篇
  2002年   5篇
  2001年   1篇
  2000年   3篇
  1999年   1篇
  1998年   2篇
  1997年   1篇
  1995年   2篇
  1993年   1篇
  1991年   4篇
  1990年   1篇
  1981年   1篇
  1970年   1篇
排序方式: 共有148条查询结果,搜索用时 15 毫秒
101.
102.
Effective temperatures T eff, surface gravities log  g and interstellar extinctions A V are found for 107 B stars. Distances d of the stars, which are based on the derived T eff, log  g and A V values, show good agreement with those obtained from the Hipparcos parallaxes. Comparing the T eff and log  g values with evolutionary computations, we infer masses, radii, luminosities, ages and relative ages of the stars. Empirical relations between the T eff and log  g parameters, on the one hand, and the photometric indices Q , [ c 1] and β , on the other hand, are constructed; these relations give a fast method for the T eff and log  g estimation of early and medium B stars. Inclusion of the infrared J , H and K colours into the T eff, log  g and A V determination shows that (i) the T eff and log  g parameters are altered only slightly; (ii) the A V value is rather sensitive to these colours, so an accuracy better than 0.05 mag in the JHK data is necessary for precise A V evaluation.  相似文献   
103.
We suggest a new way to establish the relation between the electron temperature t 3 within the [O  iii ] zone and the electron temperature t 2 within the [O  ii ] zone in high-metallicity  (12 + log(O/H) > 8.25)  H  ii regions. The   t 2– t 3  diagram is constructed by applying our method to a sample of 372 H  ii regions. We find that the correlation between t 2 and t 3 is tight and can be approximated by a linear expression. The new   t 2– t 3  relation can be used to determine t 2 and accurate abundances in high-metallicity H  ii regions with a measured t 3. It can also be used in conjunction with the ff relation for the determination of t 3 and t 2 and oxygen abundances in high-metallicity H  ii regions, where the [O  iii ]λ4363 auroral line is not detected. The derived   t 2– t 3  relation is independent of photoionization models of H  ii regions.  相似文献   
104.
105.
In October 2005 spatial distribution of live and dead Acartia clausi and Acartia tonsa was studied in the Black and Marmara Seas and near the Marmara Sea inlet of the Bosphorus, in order to understand their fate upon transportation between two seas. The morphometric characteristics in both species from all studied areas, and the decreased abundance of A. clausi and A. tonsa from the Black Sea towards the Marmara Sea indicate that the Marmara Sea Acartia populations are formed by recruitment from the Black Sea. We observed mass mortality of A. clausi in the Marmara Sea near the Prince Islands. The majority of carcasses (66% of total A. clausi numbers in the Marmara Sea) were found in the salinity gradient layer.  相似文献   
106.
107.
A natural shockwave event led to the formation of a new crystalline polymorph of carbon in gneisses from the Popigai crater, Russia. The new species occupies the interior of a multiphase assemblage and is entirely enveloped by lonsdaleite and graphite. Polishing hardness of this new phase is greater than that of lonsdaleite. Micro-beam synchrotron X-ray diffraction, imaging and fluorescence studies revealed a pure transparent carbon phase. The diffraction pattern is indexed in terms of a cubic cell (a=14.697 Å, space group Pm3m.). This species was neither encountered in static or dynamic high-pressure experiment nor predicted by theoretical calculations. To cite this article: A. El Goresy et al., C. R. Geoscience 335 (2003).  相似文献   
108.
109.
The acid/base properties of the hematite/water interface and surfacecomplexation with gold has been studied by potentiometric titrations in thefour component system H+ – FeOH –AuCl 4 - – Cl-. Equilibrium measurementswere performed in NaCl media at 298.2 K. In the evaluation of equilibriummodel from experimental data the constant capacitance model was applied. Theacid/base properties were investigated in 0.1 M NaCl in the range 2.6 pH 7.4. The resulting intrinsic constants for protonation anddeprotonation of hydroxyl groups at the surface were log 1,1,0,0(int) s = 7.10 ± 0.06 andlog -1,1,0,0(int) s = - 7.80 ±0.06. The density of proton active surface sites was 2.85nm-2 and the specific capacitance 2.5 C V-1 m-2. In the investigation of surface complexation of gold, thepotentiometric titrations were performed in the range 2.0 pH 10.2.Titration data was supplemented with analysis of Au in the aqueous phase byatomic absorbance spectrometry. The equilibrium model proposed consists ofthe following monodentate surface complexes: FeOHAuCl3(log 0,1,1,-1 s = 1.45 ± 0.03),FeOHAuCl2OH (log -1,1,1,-2 s = -3.89 ± 0.02), FeOHAu(OH)3 (log -3,1,1,-4 s = -21.94 ± 0.05). Aslightly better fit could be obtained by assuming formation of a bidentatecomplex with the composition(FeO)2Au(OH)H2O. However, based onstructural arguments this complex was rejected.  相似文献   
110.
Using powder X-ray diffraction of heated solids to pressures reaching 68 GPa, the pressure-volume-temperature (PVT) data on corundum Al2O3 and ɛ-Fe were determined with the following results: *Corundum,*Iron, *Al2O3*ɛ-Fe Isothermal bulk*258 (2)*164 (3)  modulus K'300, 1 (GPa) Pressure derivative K300, 1*4.88 (4)*5.36 (16) Temperature derivative*–0.020 (2)*–0.043 (3)  (∂K T,1 /∂T) P (GPa/K) Molar volume V300,1*25.59 (2)*6.76 (2)  (cm3/mol) Isobaric thermal expansion at 1 atm (0.101 MPa) is given by (K–1): α T =2.6 (2) 10–5+1.81 (9) 10–9 T–0.67 (6)/T 2 for corundum, and α T =5.7 (4) 10–5+4.2 (4) 10–9 T–0.17 (7)/T 2 for iron ɛ-Fe. Received: 1 March 1997 / Revised, accepted: 21 August 1997  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号