87 research outputs found

    Physiological Response to Salt (NaCl) Stress in Selected Cultivated Tetraploid Cottons

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    In the southwestern and western Cotton Belt of the U.S. soil salinity can reduce cotton productivity and quality. This study was conducted to determine the physiological responses of six genotypes including five Upland cotton (Gossypium hirsutum L.) cultivars and one Pima cotton line (G. barbadense L.) to NaCl under greenhouse conditions. Seeds were germinated and grown for 14 days prior to salt treatment (daily 100 ml of 200 mM NaCl) for 21 days. Compared with the control (daily 100 ml tap water), the NaCl treatment significantly reduced plant height, leaf area, fresh weight, and dry weight. The NaCl stress also significantly increased leaf chlorophyll content, but did not affect leaf fluorescence. Of the six genotypes, Pima 57-4 and SG 747 had the most growth reduction, and were most sensitive to NaCl; DP 33B, JinR 422 and Acala Phy 72 had the least growth reduction and were most NaCl tolerant. Although all the six genotypes under the salt treatment had significantly higher Na and Cl accumulation in leaves, SG 747 and Pima 57-4 accumulated more Na and Cl than DP 33B. Increases in leaf N, Zn, and Mn concentrations were also observed in the NaCl-treated plants. While leaf P, Ca, and S concentrations remained unchanged overall in the genotypes tested, leaf K, Mg, Fe, and Cu concentrations significantly decreased during salt stress. Reduction in plant height is a simple, easy, sensitive, non-destructive measurement to evaluate salt tolerance in cotton

    John M. Hughs correspondence with H. W. Walter, 1863 June 17

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    Letter from Colonel Hughs to Colonel Walter describing theft of horses and food as well as the destruction of property in Tennessee by Confederate forces

    Neuroblastoma cell fusion by a temperature-sensitive mutant of vesicular stomatitis virus.

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    A temperature sensitive mutant of vesicular stomatitis virus which does not mature properly when grown at 39°C promoted extensive fusion of murine neuroblastoma cells at this nonpermissive temperature. Polykaryocytes apparently formed as a result of fusion from within the cells that requires low doses of infectious virions for its promotion and is dependent on viral protein synthesis. Although 90% of infected N-18 neuroblastoma cells were fused by 15 h after infection, larger polykaryocytes continued to form, leading to an average of 28 nuclei per polykaryocyte as a result of polykaryocytes fusing to each other. Two neuroblastoma cell lines have been observed to undergo fusion, whereas three other cell lines (BHK-21, CHO, and 3T3) were incapable of forming polykaryocytes, suggesting that nervous system-derived cells are particularly susceptible to vesicular stomatitis virus-induced fusion. Although the normal assembly of the protein components of this virus is deficient at 39°C, the G glycoprotein was inserted into the infected cell membranes at this temperature. Two lines of evidence suggest that the expression of G at the cell surface promotes this polykaryocyte formation: (i) inhibition of glycosylation, which may be involved in the migration of the G protein to the cellular plasma membranes, will inhibit the cell fusion reaction; (ii) addition of antiserum, directed toward the purified G glycoprotein, will also inhibit cell fusion
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