The Carrying Capacity of Pure and Oversown Giant Star Grass (\u3ci\u3eCynodon nlemfuensis\u3c/i\u3e Vanderyst) under Different Stocking Rate in South-Western Islands of Japan

The objective of this study was firstly to know the potential carrying capacity, pasture production, pasture utilization of giant star grass under different stocking rates in intensive rotational grazing system, and to evaluate a carrying capacity of giant star grass (Cynodon nlemfuensis Vanderyst) pasture oversown with annual hybrid ryegrass (Lolium multiflorum X Lolium perenne) on short low productive winter pasture in South-western Islands of Japan. High herbage availability and good quality forage to bring about effective animal productions were produced by using relatively heavy stocking rates of 6 - 8 heads/ha, and achieved optimum pasture utilization of giant star grass. Herbage utilization and daily dry matter intake on pasture oversown with ryegrass were higher than pure giant star grass during winter. Average herbage availability and utilization at heavy stocking rate was higher than at light stocking rate even in winter

Pulsed Power Production of Ozone in 02/N2 iin a Coaxial Reactor without Dielectric Layer

Very short duration pulsed streamer discharges have been used to produce ozone in a gas mixture of nitrogen and oxygen at atmospheric pressure. The ratio of nitrogen to oxygen in the mixture was varied in the range from 2.5/0.5 to 0.5/2.5, while maintaining a total flow rate of 3 l/min. The production of ozone was found to be higher for a specific mixture ratio of N2/O2 than that in oxygen or in dry air. The production of ozone in O2 was higher than that in dry air. The production yield of ozone (g/kWh) increased with decreasing nitrogen in the O2/N2 mixture. It has been found that the peak of the streamer discharge current decreased with time after application of the pulsed power. This decrease in the current corresponded with the increase in the ozone production and is attributed to the loss of electrons in the discharge current due to their attachment to ozone to form negative ions

Ozone Production Using Pulsed Dielectric Barrier Discharge in Oxygen

The production of ozone was investigated using a dielectric barrier discharge in oxygen, and employing short-duration pulsed power. The dependence of the ozone concentration (parts per million, ppm) and ozone production yield (g(O3)/kWh) on the peak pulsed voltage (17.5 to 57.9 kV) and the pulse repetition rate (25 to 400 pulses/s, pps) were investigated. In the present study, the following parameters were kept constant: a pressure of 1.01×105 Pa, a temperature of 26±4°C a gas flow rate of 3.0 1/min and a gaseous gap length of 11 mm. A concentric coaxial cylindrical reactor was used. A spiral copper wire (1 mm in diameter) was wound on a polyvinylchloride (PVC) cylindrical configuration (26 mm in diameter) and placed centrally in a concentric coaxial electrode system with 4 mm thick PVC dielectric layer adjacent to a copper outer electrode of 58 mm in internal diameter. HV and current pulses were provided by a magnetic pulse compressor power source

Spectroscopy of 32Ne and the Island of Inversion

We report on the first spectroscopic study of the N=22 nucleus 32Ne at the newly completed RIKEN Radioactive Ion Beam Factory. A single gamma-ray line with an energy of 722(9) keV was observed in both inelastic scattering of a 226 MeV/u 32Ne beam on a Carbon target and proton removal from 33Na at 245 MeV/u. This transition is assigned to the de-excitation of the first J^pi = 2+ state in 32Ne to the 0+ ground state. Interpreted through comparison with state-of-the-art shell model calculations, the low excitation energy demonstrates that the Island of Inversion extends to at least N=22 for the Ne isotopes.Comment: Accepted for publication in Phys. Rev. Lett. 11 pages, 3 figure

Epigenetic regulation of S100 protein expression

S100 proteins are small, calcium-binding proteins whose genes are localized in a cluster on human chromosome 1. Through their ability to interact with various protein partners in a calcium-dependent manner, the S100 proteins exert their influence on many vital cellular processes such as cell cycle, cytoskeleton activity and cell motility, differentiation, etc. The characteristic feature of S100 proteins is their cell-specific expression, which is frequently up- or downregulated in various pathological states, including cancer. Changes in S100 protein expression are usually characteristic for a given type of cancer and are therefore often considered as markers of a malignant state. Recent results indicate that changes in S100 protein expression may depend on the extent of DNA methylation in the S100 gene regulatory regions. The range of epigenetic changes occurring within the S100 gene cluster has not been defined. This article reviews published data on the involvement of epigenetic factors in the control of S100 protein expression in development and cancer

DC Breakdown Voltage of Carbon Dioxide Medium under Needle to Plane Electrode

This paper reports the experimental results on thecorona onset voltage and breakdown voltage by positiveand negative dc discharges in carbon dioxide mediumwithin the pressure range of 0.1 to 15MPa under theneedle to plane electrode. From the experimental resultsof dc discharge, negative corona discharges are observedmore clearly in liquid and supercritical phase than in gasphase of carbon dioxide. However, in our experimentalcondition, positive corona discharge was not found for dcdischarges. The breakdown mechanism in liquid can beclassified into two categories on account of the bubbletriggeredformation

Epigenetic deregulation of multiple S100 gene family members by differential hypomethylation and hypermethylation events in medulloblastoma

Deregulated expression of genes encoding members of the S100 family of calcium-binding proteins has been associated with the malignant progression of multiple tumour types. Using a pharmacological expression reactivation approach, we screened 16 S100 genes for evidence of epigenetic regulation in medulloblastoma, the most common malignant brain tumour of childhood. Four family members (S100A2, S100A4, S100A6 and S100A10) demonstrated evidence of upregulated expression in multiple medulloblastoma cell lines, following treatment with the DNA methyltransferase inhibitor, 5′-aza-2′-deoxycytidine. Subsequent analysis revealed methylation of critical CpG sites located within these four genes in an extended cell line panel. Assessment of these genes in the non-neoplastic cerebellum (from which medulloblastomas develop) revealed strong somatic methylation affecting S100A2 and S100A4, whereas S100A6 and S100A10 were unmethylated. Assessed against these normal tissue-specific methylation states, S100A6 and S100A10 demonstrated tumour-specific hypermethylation in medulloblastoma primary tumours (5 out of 40 and 4 out of 35, respectively, both 12%) and cell lines (both 7 out of 9, 78%), which was associated with their transcriptional silencing. Moreover, S100A6 hypermethylation was significantly associated with the aggressive large cell/anaplastic morphophenotype (P=0.026). In contrast, pro-metastatic S100A4 displayed evidence of hypomethylation relative to the normal cerebellum in a significant proportion primary tumours (7 out of 41, 17%) and cell lines (3 out of 9, 33%), which was associated with its elevated expression. In summary, these data characterise complex patterns of somatic methylation affecting S100 genes in the normal cerebellum and demonstrate their disruption causing epigenetic deregulation of multiple S100 family members in medulloblastoma development. Epigenetic events affecting S100 genes have potential clinical utility and merit further investigation as molecular biomarkers for this disease

Fragile X Mental Retardation Protein Regulates Proliferation and Differentiation of Adult Neural Stem/Progenitor Cells

Fragile X syndrome (FXS), the most common form of inherited mental retardation, is caused by the loss of functional fragile X mental retardation protein (FMRP). FMRP is an RNA–binding protein that can regulate the translation of specific mRNAs. Adult neurogenesis, a process considered important for neuroplasticity and memory, is regulated at multiple molecular levels. In this study, we investigated whether Fmrp deficiency affects adult neurogenesis. We show that in a mouse model of fragile X syndrome, adult neurogenesis is indeed altered. The loss of Fmrp increases the proliferation and alters the fate specification of adult neural progenitor/stem cells (aNPCs). We demonstrate that Fmrp regulates the protein expression of several components critical for aNPC function, including CDK4 and GSK3β. Dysregulation of GSK3β led to reduced Wnt signaling pathway activity, which altered the expression of neurogenin1 and the fate specification of aNPCs. These data unveil a novel regulatory role for Fmrp and translational regulation in adult neurogenesis