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1.
本文利用KDV方程所对应的线性方程解所具有的光滑效应及压缩映像原理,得到了Hirota-Satsuma系统初值问题的局部和整体适定性结果. 相似文献
2.
The vibronic vapour phase photoacoustic spectrum of Br2 in the wavelength region 505–541 nm (19796–18480 cm−1) has been recorded using microphone as well as pump-probe method. Discrete vibronic bands superimposed on a monotonically
increasing continuum background towards the dissociation limit results from the overlapping B
3Π
0u
/+
← X
1Σ
g
/+
and 1Π1u
← X
1Σ
g
/+
electronic transitions. Vibronic bands originating from υ″=0 have been used to estimate the relative rate of non-radiative relaxation as a function of the excited state B
3Π0u
vibrational quantum number υ′. A comparison with the optical absorption spectroscopy of Br2 leads to the identification of three broad spectral regions between 505 and 541 nm (19796 and 18480 cm−1) on the basis of different non-radiative relaxation processes. 相似文献
3.
4.
Hicks WA Halligan BD Slyper RY Twigger SN Greene AS Olivier M 《Journal of the American Society for Mass Spectrometry》2005,16(6):916-925
Stable isotope labeling with (18)O is a promising technique for obtaining both qualitative and quantitative information from a single differential protein expression experiment. The small 4 Da mass shift produced by incorporation of two molecules of (18)O, and the lack of available methods for automated quantification of large data sets has limited the use of this approach with electrospray ionization-ion trap (ESI-IT) mass spectrometers. In this paper, we describe a method of acquiring ESI-IT mass spectrometric data that provides accurate calculation of relative ratios of peptides that have been differentially labeled using(18)O. The method utilizes zoom scans to provide high resolution data. This allows for accurate calculation of (18)O/(16)O ratios for peptides even when as much as 50% of a (18)O labeled peptide is present as the singly labeled species. The use of zoom scan data also provides sufficient resolution for calculating accurate ratios for peptides of +3 and lower charge states. Sequence coverage is comparable to that obtained with data acquisition modes that use only MS and MS/MS scans. We have employed a newly developed analysis software tool, ZoomQuant, which allows for the automated analysis of large data sets. We show that the combination of zoom scan data acquisition and analysis using ZoomQuant provides calculation of isotopic ratios accurate to approximately 21%. This compares well with data produced from (18)O labeling experiments using time of flight (TOF) and Fourier transform-ion cyclotron resonance (FT-ICR) MS instruments. 相似文献
5.
From the transport studies in the bilayer manganites LaSr2−x
Ca
x
Mn2O7, we have found the variable-range hopping model proposed by Viret et al to be inadequate to describe the transport of charge in these materials. The polarons appear to hop to their nearest neighbors
with an activation energy, which in part is dependent on the magnetic interactions in the lattice. 相似文献
6.
Ki Hwan Bae 《中国化学快报》2009,20(11):1321-1323
Phytochemical study on the BuOH-soluble fraction of the stem bark of Populus davidiana resulted in the isolation of a new salicin derivative(1),named davidianoside.The structure was elucidated on the basis of extensive physicochemical and spectroscopic analyses. 相似文献
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8.
Halligan BD Slyper RY Twigger SN Hicks W Olivier M Greene AS 《Journal of the American Society for Mass Spectrometry》2005,16(3):302-306
The main goal of comparative proteomics is the quantitation of the differences in abundance of many proteins between two different biological samples in a single experiment. By differentially labeling the peptides from the two samples and combining them in a single analysis, relative ratios of protein abundance can be accurately determined. Protease catalyzed (18)O exchange is a simple method to differentially label peptides, but the lack of robust software tools to analyze the data from mass spectra of (18)O labeled peptides generated by common ion trap mass spectrometers has been a limitation. ZoomQuant is a stand-alone computational tool that analyzes the mass spectra of (18)O labeled peptides from ion trap instruments and determines relative abundance ratios between two samples. Starting with a filtered list of candidate peptides that have been successfully identified by Sequest, ZoomQuant analyzes the isotopic forms of the peptides using high-resolution zoom scan spectrum data. The theoretical isotope distribution is determined from the peptide sequence and is used to deconvolute the peak areas associated with the unlabeled, partially labeled, and fully labeled species. The ratio between the labeled and unlabeled peptides is then calculated using several different methods. ZoomQuant's graphical user interface allows the user to view and adjust the parameters for peak calling and quantitation and select which peptides should contribute to the overall abundance ratio calculation. Finally, ZoomQuant generates a summary report of the relative abundance of the peptides identified in the two samples. 相似文献
9.
MVN Murthy Urjit A Yajnik KRS Balaji G Bhattacharyya Amol Dighe Shashikant Dugad ND Hari Dass PK Kabir Kamales Kar D Indumathi John G Learned Debasish Majumdar NK Mondal MVN Murthy SN Nayak Sandip Pakvasa Amitava Raychaudhuri RS Raghavan G Rajasekaran R Ramachandran Alak K Ray Asim K Ray Saurabh Rindani HS Sharatchandra Rahul Sinha Nita Sinha S Umasankar Urjit A Yajnik 《Pramana》2000,55(1-2):347-355
We have identified some important and worthwhile physics opportunities with a possible neutrino detector located in India.
Particular emphasis is placed on the geographical advantage with a stress on the complimentary aspects with respect to other
neutrino detectors already in operation. 相似文献
10.
S Chanda Sarmishtha Bhattacharyya Tumpa Bhattacharjee SS Ghugre Swapan Kumar Basu S Muralithar RP Singh B Mukherjee RK Bhowmik SN Ray 《Pramana》2001,57(1):175-179
The high spin states in N=80 139Pr have been investigated by in-beam γ-spectroscopic techniques following the reaction 130Te (14N, 5n) reaction at E=75 MeV, using a gamma detector array, consisting of seven 23% compton-suppressed high purity germanium detectors and a multiplicity
ball of fourteen bismuth germanate elements. Based on γ-γ coincidence data, the level scheme of 139Pr has been considerably extended up to 7.2 MeV excitation. Tentative spin-parity assignments are done for the newly proposed
levels on the basis of the DCO ratios corresponding to strong gates and the available information from the earlier light ion
experiments. 相似文献