Research Notes: Amylase and acid phosphatase genotypes of Glycine max, Glycine soja and Neonotonia wightii

Three amylase loci, Am-1, Am-2 , and Am-3, have been identified by electrophoresis (Gorman and Kiang , 1978) . The activity of amylase at Am-1 and Am-2 is very weak, and that at Am-3 is much str onger. Based on heat lability and chemical reaction, Reiss (1978) concluded Am-1 and Am- 2 represent α - amylase and Am-3 β-amylase

Research Notes : United States : Linkage of electrophoretic loci

In our studies of the inheritance of various electrophoretic variants, we have examined F2 segregation data from many crosses (see Gorman, 1983, for a listing). Many of these crosses were segregating for multiple loci, allowing linkage data to be collected. Table 1 represents a sunnnary of the linkage patterns we have observed between the listed electrophoretic loci (see Gorman and Kiang, 1978; Kiang, 1981; Gorman et al., 1983, concerning the establishment of these loci)

Research Notes : United States : Inheritance of a second leucine amino-peptidase locus and tests of its linkage with other loci

In dry soybean seed, only one leucine amino peptidase (LAP) anodal band was observed by acrylamide slab gel electrophoresis (Gorman et al., 1983). This band gradually declined in intensity and disappeared in all tissues about 10-12 days after germination. Three mobility variants (Rf\u27s 0.59, 0.53,and 0.58) were observed in the band, which was controlled by a single locus (Gor-man et al., 1983; Kiang and Gorman, 1983; Gorman, 1983)

On the Antenna Beam Shape Reconstruction Using Planet Transit

The calibration of the in-flight antenna beam shape and possible beamdegradation is one of the most crucial tasks for the upcoming Planck mission. We examine several effects which could significantly influence the in-flight main beam calibration using planet transit: the problems of the variability of the Jupiter's flux, the antenna temperature and passing of the planets through the main beam. We estimate these effects on the antenna beam shape calibration and calculate the limits on the main beam and far sidelobe measurements, using observations of Jupiter and Saturn. We also discuss possible effects of degradation of the mirror surfaces and specify corresponding parameters which can help us to determine these effects.Comment: 10 pages, 8 figure

Sorting networks using k-comparators

Bibliography: leaves 160-167

An algorithmic approach to continuous location

Bibliography: pages 126-130.We survey the p-median problem and the p-centre problem. Then we investigate two new techniques for continuous optimal partitioning of a tree T with n - 1 edges, where a nonnegative rational valued weight is associated with each edge. The continuous Max-Min tree partition problem (the continuous Min-Max tree partition problem) is to cut the edges in p - 1 places, so as to maximize (respectively minimize) the weight of the lightest (respectively heaviest) resulting subtree. Thus the tree is partitioned into approximately equal components. For each optimization problem, an inefficient implementation of the algorithm is given, which runs in pseudo-polynomial time, using a previously developed algorithm and a construction. We then derive from it a much faster algorithm using a top-down greedy technique, which runs in polynomial time. The algorithms have a variety of applications among others to highway and pipeline maintenance

Research Notes : Inheritance of soybean electrophoretic variants

We have been using the technique of slab-gel electrophoresis (see Gorman and Kiang, 1977, 1978; Kiang, 1981; Kiang and Gorman, 1983, for methods) to study genetic diversity in G. max and G. soja. In last year\u27s Soybean Genet-ics Newsletter, we reported the accession-specific zymogram types (zymogram types are equivalent to phenotypes) observed in 253 named cultivars (maturi-ty groups 00-IV) for 15 enzyme systems (Gorman et al., 1982b). We have been studying the genetic basis for the differences between these zymogram types

Research Notes : Electrophoretic classification of the early maturity groups of named soybean cultivars

Over the last several years, our lab has been collecting electrophore-tic data for several enzyme systems in G. max and G. soja. While we have not yet completed analysis of all the available G. max or G. soja accessions, we have completed electrophoretic profiles for most of the named soybean cultivars in the early maturity groups (OOO-IV). We have been interested in using these electrophoretic profiles for cultivar identification, since a fairly complete identification can be made (Gorman and Kiang, 1977; and an article in preparation)

Phase-sensitive quantum effects in Andreev conductance of the SNS system of metals with macroscopic phase breaking length

The dissipative component of electron transport through the doubly connected SNS Andreev interferometer indium (S)-aluminium (N)-indium (S) has been studied. Within helium temperature range, the conductance of the individual sections of the interferometer exhibits phase-sensitive oscillations of quantum-interference nature. In the non-domain (normal) state of indium narrowing adjacent to NS interface, the nonresonance oscillations have been observed, with the period inversely proportional to the area of the interferometer orifice. In the domain intermediate state of the narrowing, the magneto-temperature resistive oscillations appeared, with the period determined by the coherence length in the magnetic field equal to the critical one. The oscillating component of resonance form has been observed in the conductance of the macroscopic N-aluminium part of the system. The phase of the oscillations appears to be shifted by $\pi$ compared to that of nonresonance oscillations. We offer an explanation in terms of the contribution into Josephson current from the coherent quasiparticles with energies of order of the Thouless energy. The behavior of dissipative transport with temperature has been studied in a clean normal metal in the vicinity of a single point NS contact.Comment: 9 pages, 7 figures, to be published in Low Temp. Phys., v. 29, No. 12, 200

Hitting Time of Quantum Walks with Perturbation

The hitting time is the required minimum time for a Markov chain-based walk (classical or quantum) to reach a target state in the state space. We investigate the effect of the perturbation on the hitting time of a quantum walk. We obtain an upper bound for the perturbed quantum walk hitting time by applying Szegedy's work and the perturbation bounds with Weyl's perturbation theorem on classical matrix. Based on the definition of quantum hitting time given in MNRS algorithm, we further compute the delayed perturbed hitting time (DPHT) and delayed perturbed quantum hitting time (DPQHT). We show that the upper bound for DPQHT is actually greater than the difference between the square root of the upper bound for a perturbed random walk and the square root of the lower bound for a random walk.Comment: 9 page