Production of Secondaries in High Energy d+Au Collisions

In the framework of Quark-Gluon String Model we calculate the inclusive spectra of secondaries produced in d+Au collisions at intermediate (CERN SPS) and at much higher (RHIC) energies. The results of numerical calculations at intermediate energies are in reasonable agreement with the data. At RHIC energies numerically large inelastic screening corrections (percolation effects) should be accounted for in calculations. We extract these effects from the existing RHIC experimental data on minimum bias and central d+Au collisions. The predictions for p+Au interactions at LHC energy are also given.Comment: 18 pages and 10 figure

The Q^2-Dependence of Nuclear Transparency for Exclusive ρ0\rho^0 Production

Exclusive coherent and incoherent electroproduction of the $\rho^0$ meson from $^1$H and $^{14}$N targets has been studied at the HERMES experiment as a function of coherence length ($l_c$), corresponding to the lifetime of hadronic fluctuations of the virtual photon, and squared four-momentum of the virtual photon ($-Q^2$). The ratio of $^{14}$N to $^1$H cross sections per nucleon, known as nuclear transparency, was found to increase (decrease) with increasing coherence length for coherent (incoherent) $\rho^0$ electroproduction. For fixed coherence length, a rise of nuclear transparency with $Q^2$ is observed for both coherent and incoherent $\rho^0$ production, which is in agreement with theoretical calculations of color transparency.Comment: 5 pages, 4 figure

Production of secondaries in soft p+pb collisions at LHC

We calculate the inclusive spectra of secondaries produced in soft (minimum bias) p+Pb collisions in the framework of Quark-Gluon String Model at LHC energy, and by taking into account the inelastic screening corrections (percolation effects). The role of these effects is expected to be very large at very high energies, and they should decrease the spectra about 3 times in the midrapidity region and increase them about 2 times in the fragmentation region at the energy of LHC.Comment: 18 pages and 10 figures. arXiv admin note: text overlap with arXiv:0802.219

Morphological and histochemical characterization of the seminiferous epithelial and Leydig cells of the turkey

Unlike mammals, there is little fundamental information about spermatogenesis in birds. This study was undertaken to clarify the morphology, histochemistry, and lectin affinity of the seminiferous epithelial cells and Leydig cells in pre-pubertal (8- to 15-week old) and adult (40- to 44-week old) domestic turkeys. In adult turkeys, three types of spermatogonia were defined based on their chromatin distribution and nuclear morphology: the dark type A(Ad); the pale type A(Ap); and the type B. The Ad is the least numerous and least conspicuous and consequently difficult to locate. Based on its spatial distribution and overall morphology, type Ad spermatogonia were postulated to be the spermatogonia stem cells in the turkey. Antibodies to c-kit were localized to spermatogonia in the pre-pubertal and to a lesser extent in adult males. Peanut agglutinin (PNA) was specific for spermatocytes in the pre-pubertal males and spermatogonia and early spermatocytes in adult males. Wheat-germ agglutinin (WGA) highlighted Sertoli cells in both age groups. Bandeiraea simplicifolia I, soybean agglutinin, and winged-pea agglutinin staining were limited to the wall of the seminiferous tubule and some extra-tubular cell types. Concanavalin A staining was diffuse and not cellspecific and, therefore, could not be used to selectively identify a particular cell type. It was concluded that WGA and PNA could aid in identifying specific cell types in the seminiferous epithelium of testis from prepubertal and mature turkeys. Only Leydig cells were alkaline phosphatase reactive in the mature turkey testes. The information from this study is being used to adapt techniques for the isolation and partial purification developed for mammalian spermatogonia to avian spermatogonia and other specific cell types in the testes

Identification of various testicular cell populations in pubertal and adult cockerels

Precise identification of the male germinal stem cell population is important for their practical use in programs dedicated to the integration of exogenous genetic material in testicular tissues. In the present study, our aim was to identify germinal cell populations in the testes of pubertal and adult cockerels based on the detection of the nuclear DNA content by fluorescence-activated cell sorting (FACS) and on the expression of the Dazl and Stra8 genes in singlecell suspensions of testicular tissues. Cells with a tetraploid DNA content (4c) represent a small and equal fraction of the total germinal cell population in both pubertal and adult males. In contrast, the diploid (2c) and haploid (c) subpopulations differ significantly between ages as a consequence of different degrees of sexual maturation. A specific subpopulation of testicular cells, the side-scatter subpopulation of cells, or side population (SP), was identified at the junction between the haploid and diploid cell populations. The percentage of this cell subpopulation differs significantly in pubertal and adult cockerels, accounting for 4.1% and 1.3% of the total cell population, respectively. These four testicular cell populationswere also tested for the expression of Dazl and Stra8 genes known to be expressed in premeiotic cells including stem spermatogonia. Both genes were expressed in SP, whereas the expression of either Dazl or Stra8 genes was detected only in the 4c and in the 2c testicular cell subpopulations, respectively. The correlation between the cell ploidy and Dazl/Stra8 expression was the same at both male ages. We conclude that SP cells might represent a subpopulation of germinal cells enriched in stem spermatogonia, which can be of great importance for transgenesis in chicken

Health effects of beer from the angle of free radicals and antioxidants.

Alcohol and mixture of antioxidants belong among the main biologically effective components in beer. The article indicates in a well-arranged from the efficiency of alcohol on organism; the ratio of the favourable and unfavourable effects depends on the amount of its daily consumption. The favourable effect of alcohol consists mainly in the increase of concentration of antiatherogenic high density lipoproteins (HDL), in inhibition of lipoperoxidation and in the antiaggregational incidence on blood platelets. In beer the antioxidants come from malt, less specifically from hops; this is mostly the question of polyphenols. The survey sums up the main physiological effects of these antioxidants; the inhibition of oxidation of low density lipoproteins (LDL), vasodilatation and the antioxidant incidence. As chelators of metals, they hedge the rice of hydroxyle radical by the Fentor reaction. The authors end by summarizing results of their own antioxidant capacity measurement of some sorts of beer.(In Czech, English summary only