Simultaneous evaluation of the shell and pairing corrections to the nuclear deformation energy

1993 ◽  
Vol 48 (4) ◽  
pp. 1656-1666 ◽  
Author(s):  
N. H. Allal ◽  
M. Fellah
1973 ◽  
Vol 203 (3) ◽  
pp. 433-472 ◽  
Author(s):  
H. Flocard ◽  
P. Quentin ◽  
A.K. Kerman ◽  
D. Vautherin

2016 ◽  
Vol 25 (03) ◽  
pp. 1650016 ◽  
Author(s):  
V. M. Kolomietz ◽  
A. I. Sanzhur ◽  
B. V. Reznychenko

In this paper, we apply the direct variational method to derive the nuclear deformation energy. The extended Thomas–Fermi approximation (ETFA) for the energy functional with Skyrme forces is used. We study the influence of the finite surface layer of the nuclear density profile function on the formation of the fission barrier and the scission configuration. Comparison of the variational approach with the traditional liquid drop model (LDM) is presented. We show the sensitivity of the numerical results to the surface diffuseness parameter.


1970 ◽  
Vol 32 (4) ◽  
pp. 229-232 ◽  
Author(s):  
K. Albrecht ◽  
D. Scharnweber ◽  
W. Greiner ◽  
U. Mosel

1976 ◽  
Vol 61 (2) ◽  
pp. 133-138 ◽  
Author(s):  
A. Faessler ◽  
R̵.R. Hilton ◽  
K.R. Sandhya Devi

Informatica ◽  
2018 ◽  
Vol 29 (2) ◽  
pp. 265-280 ◽  
Author(s):  
Mehdi Keshavarz-Ghorabaee ◽  
Maghsoud Amiri ◽  
Edmundas Kazimieras Zavadskas ◽  
Zenonas Turskis ◽  
Jurgita Antucheviciene

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 514e-514
Author(s):  
James M. Bradeen ◽  
Philipp W. Simon

The amplified fragment length polymorphism (AFLP) is a powerful marker, allowing rapid and simultaneous evaluation of multiple potentially polymorphic sites. Although well-adapted to linkage mapping and diversity assessment, AFLPs are primarily dominant in nature. Dominance, relatively high cost, and technological difficulty limit use of AFLPs for marker-aided selection and other locus-specific applications. In carrot the Y2 locus conditions carotene accumulation in the root xylem. We identified AFLP fragments linked to the dominant Y2 allele and pursued conversion of those fragments to codominant, PCR-based forms useful for locus-specific applications. The short length of AFLPs (≈60 to 500 bp) precludes development of longer, more specific primers as in SCAR development. Instead, using sequence information from cloned AFLP fragments for primer design, regions outside of the original fragment were amplified by inverse PCR or ligation-mediated PCR, cloned, and sequenced. Differences in sequences associated with Y2 vs. y2 allowed development of simple PCR assays differentiating those alleles. PCR primers flanking an insertion associated with the recessive allele amplified differently sized products for the two Y2 alleles in one assay. This assay is rapid, technologically simple (requiring no radioactivity and little advanced training or equipment), reliable, inexpensive, and codominant. Our PCR assay has a variety of large scale, locus-specific applications including genotyping diverse carrot cultivars and wild and feral populations. Efforts are underway to improve upon conversion technology and to more extensively test the techniques we have developed.


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