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51.
Aubert B Barate R Boutigny D Couderc F Karyotakis Y Lees JP Poireau V Tisserand V Zghiche A Grauges E Palano A Pappagallo M Pompili A Chen JC Qi ND Rong G Wang P Zhu YS Eigen G Ofte I Stugu B Abrams GS Borgland AW Breon AB Brown DN Button-Shafer J Cahn RN Charles E Day CT Gill MS Gritsan AV Groysman Y Jacobsen RG Kadel RW Kadyk J Kerth LT Kolomensky YG Kukartsev G Lynch G Mir LM Oddone PJ Orimoto TJ Pripstein M Roe NA Ronan MT Wenzel WA Barrett M Ford KE Harrison TJ Hart AJ Hawkes CM Morgan SE 《Physical review letters》2005,95(4):041805
We present results from an analysis of B(0)B(0)--> rho(+)rho(-) using 232 x 10(6) Gamma (4S) --> BB decays collected with the BABAR detector at the PEP-II asymmetric-energy B factory at SLAC. We measure the longitudinal polarization fraction f(L) = 0.978 +/- 0.014(stat) + 0.021 / -0.029(syst) and the CP-violating parameters S(L)= -0.33 +/- 0.24(stat) + 0.08 / -0.14(syst) and C(L)= -0.03 +/- 0.18(stat) +/- 0.09(syst). Using an isospin analysis of B --> rhorho decays, we determine the unitarity triangle parameter alpha. The solution compatible with the standard model is alpha = (100 +/- 13) degrees. 相似文献
52.
53.
Let N denote the set of natural numbers and let P =(N
k
, ) be a countably infinite poset on the k-dimensional lattice N
k
. Given x N
k
, we write max(x) (min(x)) for the maximum (minimum) coordinate of x. Let
be the directed-incomparability graph of P which is defined to be the graph with vertex set equal to N
k
and edge set equal to the set of all (x, y) such that max(x) max(y) and x and y not comparable in P. For any subset D N
k
, we let P
D
and
D
denote the restrictions of P and
to D. Points x N
k
with min(x) = 0 will be called boundary points. We define a geometrically natural notion of when a point is interior to P or
relative to the lattice N
k
, and an analogous notion of monotone interior with respect to
or
D
. We wish to identify situations where most of these interior points are exposed to the boundary of the lattice or, in the case of monotone interior points, not concealed very much from the boundary. All of these ideas restrict to finite sublattices F
k
and/or infinite sublattices E
k
of N
k
. Our main result shows that for any poset P and any arbitarily large integer M > 0, there is an F E with F = M where, relative to the sublattices F
k
E
k
, the ideal situation of total exposure of interior points and very little concealment of monotone interior points must occur. Precisely, we prove that for any P =(N
k
, ) and any integer M > 0, there is an infinite E N and a finite D F
k
with F E and F = M such that (1) every interior vertex of P
E
k
or
E
k
is exposed and (2) there is a fixed set C E, C k
k
, such that every monotone-interior point of
D
belonging to F
k
has its monotone concealment in the set C. In addition, we show that if P
1 =(N
k
, 1),..., P
r
=(N
k
,
r
) is any sequence of posets, then we can find E,D, and F so that the properties (1) and (2) described above hold simultaneously for each P
i
. We note that the main point of (2) is that the bound k
k
depends only on the dimension of the lattice and not on the poset P. Statement (1) is derived from classical Ramsey theory while (2) is derived from a recent powerful extension of Ramsey theory due to H. Friedman and shown by Friedman to be independent of ZFC, the usual axioms of set theory. The fact that our result is proved as a corollary to a combinatorial theorem that is known to be independent of the usual axioms of mathematics does not, of course, mean that it cannot be proved using ZFC (we just couldn"t find such a proof). This puts our geometrically natural combinatorial result in a somewhat unusual position with regard to the axioms of mathematics. 相似文献
54.
Repeated freeze-thaw cycles in cryosurgery 总被引:2,自引:0,他引:2
55.
Manganese(II) iodide, iron(II) iodide and copper(I) iodide each react with tetramethylammonium disulphite to form anhydrous manganese(II) sulphite, iron(II) sulphite and copper(I) disulphite respectively. Iron(II) sulphite and copper(I) disulphite react with dimethylsulphoxide-sulphur dioxide to form iron(II) disulphate and copper(II) disulphate respectively. Hydrated sulphites of manganese(II), iron(II), magnesium(II) and calcium(II) were also prepared. The properties of the sulphites were investigated using thermogravimetric and IR measurements. 相似文献
56.
R. Bailey E. Belau T. Böhringer M. Bosman V. Chabaud C. Damerell C. Daum C. De Rijk H. Dijkstra S. Gill A. Gillman R. Gilmore Z. Hajduk C. Hardwick W. Hoogland B.D. Hyams R. Klanner T. Zeludziewicz 《Physics letters. [Part B]》1984,139(4):320-326
We have observed three unique decays of F mesons into KKπ and five unique decays of D mesons into KKπ using the NA11 spectrometer together with a telescope of high-resolution silicon microstrip detectors. The mass value obtained for the F meson is (1975 ± 4) MeV, the lifetime (3.2±1.33..0)×10?13 s. 相似文献
57.
Aubert B Barate R Boutigny D Couderc F Gaillard JM Hicheur A Karyotakis Y Lees JP Tisserand V Zghiche A Palano A Pompili A Chen JC Qi ND Rong G Wang P Zhu YS Eigen G Ofte I Stugu B Abrams GS Borgland AW Breon AB Brown DN Button-Shafer J Cahn RN Charles E Day CT Gill MS Gritsan AV Groysman Y Jacobsen RG Kadel RW Kadyk J Kerth LT Kolomensky YG Kukartsev G Lynch G Mir LM Oddone PJ Orimoto TJ Pripstein M Roe NA Ronan MT Shelkov VG Wenzel WA Ford KE Harrison TJ Hawkes CM Morgan SE Watson AT 《Physical review letters》2004,93(18):181806
We search for B meson decays into two-body combinations of eta, eta', omega, and phi mesons from 89 x 10(6) BB pairs collected with the BABAR detector at the PEP-II asymmetric-energy e+e- collider at SLAC. We find the branching fraction B(B0-->etaomega)=(4.0(+1.3)(-1.2)+/-0.4)x10(-6) with a significance of 4.3 sigma. For the other decay modes we set the following 90% confidence level upper limits on the branching fractions, in units of 10(-6): B(B0-->etaeta)<2.8, B(B0-->etaeta')<4.6, B(B0-->eta'eta')<10, B(B0-->eta'omega)<2.8, B(B0-->etaphi)<1.0, B(B0-->eta'phi)<4.5, and B(B0-->phiphi)<1.5. 相似文献
58.
Aubert B Barate R Boutigny D Gaillard JM Hicheur A Karyotakis Y Lees JP Robbe P Tisserand V Zghiche A Palano A Pompili A Chen JC Qi ND Rong G Wang P Zhu YS Eigen G Ofte I Stugu B Abrams GS Borgland AW Breon AB Brown DN Button-Shafer J Cahn RN Charles E Day CT Gill MS Gritsan AV Groysman Y Jacobsen RG Kadel RW Kadyk J Kerth LT Kolomensky YG Kral JF Kukartsev G LeClerc C Levi ME Lynch G Mir LM Oddone PJ Orimoto TJ Pripstein M Roe NA Romosan A Ronan MT Shelkov VG Telnov AV Wenzel WA Ford K 《Physical review letters》2003,91(22):221802
We present evidence for the flavor-changing neutral current decay B-->K*l+l- and a measurement of the branching fraction for the related process B-->K l+l-, where l+l- is either an epsilon+epsilon- or a mu+mu- pair. These decays are highly suppressed in the standard model, and they are sensitive to contributions from new particles in the intermediate state. The data sample comprises 123 x 10(6) Upsilon(4S)-->B(-)B decays collected with the BABAR detector at the SLAC PEP-II epsilon+epsilon- storage ring. Averaging over K(*) isospin and lepton flavor, we obtain the branching fractions B(B-->Kl+l-)=(0.65(+0.14)(-0.13)+/-0.04)x10(-6) and B(B-->K*l+l-)=(0.88(+0.33)(-0.29)+/-0.10)x10(-6), where the uncertainties are statistical and systematic, respectively. The significance of the B-->Kl+l- signal is over 8sigma, while for B-->K*l+l- it is 3.3sigma. 相似文献
59.
Nonlinear grassland responses to past and future atmospheric CO(2) 总被引:17,自引:0,他引:17
Carbon sequestration in soil organic matter may moderate increases in atmospheric CO(2) concentrations (C(a)) as C(a) increases to more than 500 micromol mol(-1) this century from interglacial levels of less than 200 micromol mol(-1) (refs 1 6). However, such carbon storage depends on feedbacks between plant responses to C(a) and nutrient availability. Here we present evidence that soil carbon storage and nitrogen cycling in a grassland ecosystem are much more responsive to increases in past C(a) than to those forecast for the coming century. Along a continuous gradient of 200 to 550 micromol mol(-1) (refs 9, 10), increased C(a) promoted higher photosynthetic rates and altered plant tissue chemistry. Soil carbon was lost at subambient C(a), but was unchanged at elevated C(a) where losses of old soil carbon offset increases in new carbon. Along the experimental gradient in C(a) there was a nonlinear, threefold decrease in nitrogen availability. The differences in sensitivity of carbon storage to historical and future C(a) and increased nutrient limitation suggest that the passive sequestration of carbon in soils may have been important historically, but the ability of soils to continue as sinks is limited. 相似文献
60.
Read TD Peterson SN Tourasse N Baillie LW Paulsen IT Nelson KE Tettelin H Fouts DE Eisen JA Gill SR Holtzapple EK Okstad OA Helgason E Rilstone J Wu M Kolonay JF Beanan MJ Dodson RJ Brinkac LM Gwinn M DeBoy RT Madpu R Daugherty SC Durkin AS Haft DH Nelson WC Peterson JD Pop M Khouri HM Radune D Benton JL Mahamoud Y Jiang L Hance IR Weidman JF Berry KJ Plaut RD Wolf AM Watkins KL Nierman WC Hazen A Cline R Redmond C Thwaite JE White O Salzberg SL Thomason B Friedlander AM Koehler TM Hanna PC 《Nature》2003,423(6935):81-86
Bacillus anthracis is an endospore-forming bacterium that causes inhalational anthrax. Key virulence genes are found on plasmids (extra-chromosomal, circular, double-stranded DNA molecules) pXO1 (ref. 2) and pXO2 (ref. 3). To identify additional genes that might contribute to virulence, we analysed the complete sequence of the chromosome of B. anthracis Ames (about 5.23 megabases). We found several chromosomally encoded proteins that may contribute to pathogenicity--including haemolysins, phospholipases and iron acquisition functions--and identified numerous surface proteins that might be important targets for vaccines and drugs. Almost all these putative chromosomal virulence and surface proteins have homologues in Bacillus cereus, highlighting the similarity of B. anthracis to near-neighbours that are not associated with anthrax. By performing a comparative genome hybridization of 19 B. cereus and Bacillus thuringiensis strains against a B. anthracis DNA microarray, we confirmed the general similarity of chromosomal genes among this group of close relatives. However, we found that the gene sequences of pXO1 and pXO2 were more variable between strains, suggesting plasmid mobility in the group. The complete sequence of B. anthracis is a step towards a better understanding of anthrax pathogenesis. 相似文献