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  • 1
    ISSN: 1432-1939
    Keywords: Key wordsAvicennia germinans ; Cell elasticity ; Ion accumulation ; Osmotic potential ; Salinity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Physiological traits involved in leaf water relations were evaluated in Avicennia germinans (L.) L. seedlings growing at different salinities in the field. Analysis of pressure-volume (P-V) curves and sap osmometry were combined to evaluate osmotic adjustment and cell elasticity, and the contribution of accumulated inorganic ions to osmotic potential was estimated. Seedlings growing in soils with interstitial water salinity above that of normal sea water showed a modification of the relationship between water potential and relative water content. Thus, their leaf osmotic potential at maximum turgor (Ψπ( max )) and at zero turgor (Ψπ(0)) was 1.41 and 1.82 MPa lower respectively, than that of the seedlings from the low salinity site. Volumetric moduli of elasticity () were between 17 and 23 MPa. Thus, ɛ was about 6 MPa lower in high-salinity plants indicating that their cells were slightly more elastic. Ionic concentration analysis showed that Σ [anions] and Σ [cations] were higher in the high-salinity site (22–35%) while the water content per unit dry mass was only 12–17% lower. Reduction in water content was insufficient to explain the increase in ion concentration. Ion concentration explained 73 and 66% of the osmotic potential estimated by P-V curves for leaves from low- and high-salinity sites, respectively. In conclusion, this study provided evidence that leaves of A. germinans seedlings adapt to hypersaline soils by increasing solute concentration by 52% and cell elasticity by 26%. Both processes allow leaf water uptake and turgor maintenance over a large range of soil water potential.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 641-648 
    ISSN: 0887-6266
    Keywords: polyethylene ; glass transition ; TSDC ; γ transition ; β transition ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: New thermally stimulated depolarization currents (TSDC) results on LLD polyethylene functionalized with diethylmaleate polar groups are precisely computer fitted with the direct signal analysis technique. It is shown that the TSDC spectrum consists, with increasing temperatures, of a sub-γ peak, a sharp γ peak, and a β and an α relaxation. The first peak is analyzed in terms of Arrhenius relaxation times, whereas the γ and β transitions could only be fitted by using Vogel-Fulcher temperature dependence for the relaxation times. The best value for To obtained from both fittings is 69.7 K. This is a quantitative proof for the identification of the γ transition as one of the dielectric manifestations of the glass-rubber transition for polyethylenes, Tg = 136.5 K, which has been discussed extensively in the literature. The β relaxation, Tgβ = 237 K, has also the expected characteristic of a glass transition; the existence of two Tgs in polyethylene could explain our results. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 1259-1267 
    ISSN: 0887-6266
    Keywords: liquid crystals ; thermotropic polyesters ; relaxations ; phase transitions ; mesophases ; dielectric relaxations ; thermally stimulated depolarization current experiments ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The relaxation behavior of poly(tetra ethylene oxide terephthaloyl-bis-4-oxybenzoate), PTETOB, was analyzed by thermally stimulated depolarization currents, TSDC, and dynamic mechanical techniques, DMTA, and the results compared with those obtained by differential scanning calcrimetry, thermo-optical analysis, and x-ray diffraction. In the low temperature region, -173-30°C, three main transitions were observed and assigned to the γ relaxation, the glass transition of the mesophase and the glass transition temperature of the amorphous material. The complex behavior observed in the range 110-160°C was as signed to a crystal-crystal transition which competed with the formation of a mesophase and afterward the formation of a smectic A mesophase. At higher temperatures, was observed the transition from the smectic A mesophase to a nematic one, prior to the isotropization temperature. In the TSDC experiments the formation of a permanent electret was detected and the charges trapped in the mesophase were canceled only at the isotropization temperature. © 1995 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2483-2493 
    ISSN: 0887-6266
    Keywords: polyvynilidenefluoride ; glass transition ; thermally stimulated depolarization current ; dielectric loss ; relaxation times distribution ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The αa-mode (associated to the dynamic glass transition) in PVDF-α has been studied by Thermally Stimulated Depolarization Currents (TSDC) and Dielectric Spectroscopy (DS) techniques. The distribution of relaxation parameters, reorientation energies, characteristic temperature, and preexponential factors of the Vogel-Tammann-Fulcher relaxation times have been precisely determined by using the Simulated Annealing Direct Signal Analysis applied to a partially discharged TSDC αa peak. This distribution has been used to predict the variation of the dielectric loss, ε″(ω, T), in the temperature and frequency range where the DS measurements were made on the same material. The simulated ε′(T, ω) for various ω, are compared to the experimental values. The width of the peak is always too low, due to the restricted distribution used for the generation of the curves. A relaxation map including the TSDC results is used to determine the relaxation time variation. In the limited frequency range where the AC DS experiments are performed (102 ≤ f ≤ 105 Hz) a master curve is drawn and the exponents of the frequency dependence are found at low and high frequency; also, a fitting to the Havriliak-Negami distribution is successfully performed. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2483-2493, 1997
    Additional Material: 6 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2863-2879 
    ISSN: 0887-6266
    Keywords: semicrystalline polymers ; polycarbonate ; TSDC ; rigid amorphous phase ; glass transition ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thermally Stimulated Depolarization Current technique, Differential Scanning Calorimetry, and Dynamic Mechanical Analysis have been applied to amorphous and semicrystalline bisphenol-A polycarbonate with crystallinity degrees up to 21.8%, in a temperature interval covering the α and β relaxations. The secondary β transition is found to be the sum of three components whose variations in aged and annealed specimens have shown the cooperative character of the β1 and β2 modes, contrary to the localized nature of the β3 component. A Tg decrease was observed by both TSDC and DSC as a function of Xc and has been related to the possible confinement of the mobile amorphous phase in regions whose sizes are smaller than the correlation lengths of the cooperative movements that characterize the motions occurring at Tg. The α relaxation intensity variations with crystallinity show the existence of an abundant rigid amorphous phase in the semicrystalline material. The relaxation parameters deduced from the Direct Signal Analysis of the α relaxation for the mobile amorphous phase do not show significant deviations from those found for the amorphous material. The existence of the rigid amorphous phase has been associated to the ductile-to-brittle transition experienced by the material at low crystallinity levels. © 1996 John Wiley & Sons, Inc.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Publication Date: 1997-03-01
    Print ISSN: 1155-4339
    Electronic ISSN: 1764-7177
    Topics: Physics
    Published by EDP Sciences
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  • 7
    Publication Date: 1998-04-14
    Print ISSN: 0029-8549
    Electronic ISSN: 1432-1939
    Topics: Biology
    Published by Springer
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  • 8
    Publication Date: 1998-12-01
    Print ISSN: 0142-9612
    Electronic ISSN: 1878-5905
    Topics: Biology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Medicine
    Published by Elsevier
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