Effect of the magnetic field curvature on magnetic islands in tokamaks

The effect of the magnetic field curvature on magnetic islands in a tokamak is analyzed. It is demonstrated that the original investigation of this effect by Kotschenreuther et al. (1985) is inconsistent: on the one hand, the authors made the correct assumption that this is an ideal effect and, on the other hand, they described it in terms of the parameters characteristic of the “resistive ordering” approach, which is incompatible with the ideal approximation. More recent studies of the magnetic curvature effect have produced further ambiguities; as a result, a branch of the theory of magnetic islands has arisen that is based on the supposition that the effect under discussion can be described in terms of the Glasser-Greene-Johnson parameter D_R. This branch is shown to be erroneous, because the parameter D_R describes the plasma response to magnetic field perturbations on spatial scales of about the dimension of the linear resistive layer, while the characteristic spatial scale of the magnetic islands is much longer. It is concluded that the correct theory developed here for the magnetic curvature effect makes more optimistic predictions about its stabilizing role.     

Viable mutant homozygotes at Adh1 locus in sugar beet and their combination ablility

Selection for an increased frequency of mutant semilethal allele Adh1-S of the gene for alcohol dehydrogenase (ADH) was conducted in inbred families of sugar beet. Starting from the fourth generation, viable plants of mutant Adh1-SS homozygotes appeared. In the sixth generation of selection, the combinative ability of mutant homozygotes SS, normal homozygotes FF, and heterozygotes FS was estimated. The hybrids of mutant homozygotes outperformed the hybrids of normal homozygotes in all parameters examined (germinating capacity of seeds, length and weight of 1-week shoots, chlorophyll content in leaves, and root weight). The hybrids of heterozygotes had intermediate values of the parameters. The results obtained are discussed with regard to the mechanisms underlying the recovery of viability of mutant homozygotes and the formation of a compensating gene complex (CGC).     

Hippocampus morphology in tissue culture]

Explants of the hippocampus of newborn rats were studied neurohistologically and with electron microscope within 5--35 days of explantation. Two zones are found in the culture of the hippocampus: a zone of explant, and a zone of outgrowth. Neurons, glial cells and a network of their fibres are compactly arranged in the center of the former, whereas, the latter involves a layer of migrated glial cells. The explant is surrounded by glia limiting cells. Three types of neurons are identified in the long living culture of the hippocampus: pyramidal, polymorphic and granule cells. Numerous nerve endings observed in the hippocampic explant can be recognized as axodendritic, axosomatic and glomerular synapses. The availability of several types of neurons, a variety of synapses and their complication during outgrowth of the culture are suggestive of a formation in the hippocampic explant of a functional reflex activity.     

Microstructural analysis of the effects of incorporation of myelin basic protein in phospholipid layers

We report an X-ray reflectivity study on the effects of adsorption of myelin basic protein (MBP) on Langmuir monolayers and on deposited Langmuir–Schaefer multilayers of the phospholipid dipalmitoyl phosphatidylglycerol (DPPG). We provide for the first time, direct microscopic evidence on the destructuring effects of MBP leading to plasticity of the DPPG layers supporting commonly accepted models of the stabilizing role of MBP in the myelin membrane. We also show how protein adsorption onto the layer is determined both by electrostatic and nonspecific hydrophobic interactions.     

Studying plant genome variation using molecular markers

The authors' studies on the organization and variation of plant genome with the use of molecular markers are briefly reviewed with special emphasis on random amplified polymorphic DNA (RAPD), inter simple sequence repeat (ISSR), sequence characterized amplified region (SCAR), and cleaved amplified polymorphic sequence (CAPS) markers detected with the use of polymerase chain reaction (PCR). These markers have been demonstrated to be promising for identifying cultivars and determining the purity of genetic strains of pea. Genetic relationships between strains, cultivars, and mutants of pea have been studied. The role of molecular markers in molecular genetic mapping and localizing the genes of commercially important characters of pea has been shown. The possibility of the use of molecular markers for studying somaclonal variation and detecting mutagenic factors in plants during long-term spaceflights is considered. The prospects of using DNA markers for understanding the organization and variability of higher plant genomes are discussed.     

A CAPS marker set for mapping in linkage group III of pea (Pisum sativum L.)

A set of twelve CAPS markers was mapped for linkage group III of pea (Pisum sativum L.). New primers were designed to use a polymerase chain reaction to amplify fragments of sequenced pea genes containing at least one large intron. Amplification products were tested for polymorphism across three pea lines (Chi115, Flagman and WL1238) using eleven four-base restriction endonucleases. Nine STS markers for linkage group III from the literature were also tested for polymorphism, and five of these were used in this mapping study as anchor points. All polymorphic loci were located by genetic analysis of the F(2)population from the cross Chi115 x WL1238, and a map of linkage group III consisting of one morphological and twelve CAPS markers was created. The map covers the full length of the chromosome and is about 162 cM long. All the CAPS markers in a set were used to test for polymorphism among 10 additional pea DNA samples extracted from different marker lines and cultivars.     

Lack of direct DNA damage in human blood leukocytes and lymphocytes after in vitro exposure to high power microwave pulses

Currently, the potential genotoxicity of high power microwave pulses (HPMP) is not clear. Using the alkaline single cell gel electrophoresis assay, also known as the alkaline comet assay, we studied the effects of HPMP (8.8 GHz, 180 ns pulse width, peak power 65 kW, pulse repetition frequency 50 Hz) on DNA of human whole-blood leukocytes and isolated lymphocytes. The cell suspensions were exposed to HPMP for 40 min in a rectangular waveguide. The average SAR calculated from the temperature kinetics was about 1.6 kW/kg (peak SAR was about 300 MW/kg). The steady-state temperature rise in the 50 microl samples exposed to HPMP was 3.5 +/- 0.1 degrees C. In independent experiments, we did not find any statistically significant DNA damage manifested immediately after in vitro HPMP exposure of human blood leukocytes or lymphocytes or after HPMP exposure of leukocytes subsequently incubated at 37 degrees C for 30 min. Our results indicate that HPMP under the given exposure conditions did not induce DNA strand breaks, alkali-labile sites, and incomplete excision repair sites, which could be detected by the alkaline comet assay.