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  • 1
    Publication Date: 2017-04-04
    Description: We report systematic spatial variations of fault rocks along non-planar strike-slip faults 11 cross-cutting the Lake Edison Granodiorite, Sierra Nevada, California (Sierran wavy fault) and 12 Lobbia outcrops of the Adamello Batholith in the Italian Alps (Lobbia wavy fault). In the case of 13 the Sierran fault, pseudotachylyte formed at contractional fault bends, where it is found as thin 14 (1-2 mm) fault-parallel veins. Epidote and chlorite developed in the same seismic context as the 15 pseudotachylyte and are especially abundant in extensional fault bends. We argue that the 16 presence of fluids, as illustrated by this example, does not necessarily preclude the development 17 of frictional melt. In the case of the Lobbia fault, pseudotachylyte thickness varies along the 18 length of the fault, but the pseudotachylyte veins thicken and pool in extensional bends. We 19 conduct a quantitative analysis of fault roughness, microcrack distribution, stress, and friction 20 along the Lobbia fault. 21 Numerical modeling results show that opening in extensional bends and localized thermal 22 weakening in contractional bends counteract resistance encountered by fault waviness, resulting 23 in an overall weaker fault than suggested by the corresponding static friction coefficient. The 24 models also predict static stress redistribution around bends in the faults which are consistent 25 with distributions of microcracks, indicating significant elastic and inelastic strain energy is 26 dissipated into the wall rocks due to non-planar fault geometry. Together these observations suggest that damage and energy dissipation occurs along the entire non-planar fault during slip, 28 rather than being confined to the region close to the dynamically propagating crack tip.
    Description: Published
    Description: 3.1. Fisica dei terremoti
    Description: JCR Journal
    Description: open
    Keywords: earthquakes ; rutpure ; 04. Solid Earth::04.04. Geology::04.04.99. General or miscellaneous
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 15 (1976), S. 295-297 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 16 (1951), S. 1121-1125 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 21 (1956), S. 530-533 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 21 (1949), S. 1474-1476 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 74 (1952), S. 2106-2107 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 73 (1951), S. 5455-5456 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-1424
    Keywords: Sodium ; Urea ; Symport ; Cotransport ; Charophytes ; Slip model
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract We have previously investigated the electrogenic influx of urea in Chara, and the urea- and sodium-dependent membrane current. We have shown that there is a sodium-stimulated component of urea influx and a urea-stimulated component of sodium influx, and that these are of the same size. We conclude that the electrogenic inward transport of urea, and of its analogues acetamide and acrylamide, is by sodium symport, with a stoichiometric ratio of 1∶1. The kinetics of the fluxes and currents show two different K M values for sodium in different cells and two different kinds of kinetics for the effect of urea on membrane current, one of which fits the Michaelis-Menten equation, while the other shows a maximum and fits the difference of two Michaelis-Menten terms, suggesting a phenomenon like cis-inhibition. Similarities in kinetic characteristics between the inhibitory site and the electrically silent uptake site (System II) lead us to suggest that the same protein may be responsible for both the low-K M, electrogenic influx of urea (System I) and the high-K M, electrically silent influx by System II. We suggest a “slip” model for urea uptake in Chara.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-1424
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary Although it is generally believed thatChara and some fresh-water angiosperms transport bicarbonate ions inwards across their plasma membranes, there has been no direct demonstration of such transport in these plants. The (indirect) arguments for their transporting HCO 3 − are arguments against the inward diffusion of CO2 at the observed rates. They rest on calculations of the equilibrium concentration of CO2 or of the maximum rate at which CO2 might be produced from HCO 3 − at the pH of the medium outside the cells. SinceChara acidifies the medium over about half the cell surface during C assimilation, these calculations have been based on questionable premises. We propose a model forChara in which the acidification is attributed to active efflux of H+, and we calculate that both the equilibrium concentration of CO2 and its rate of production outside the cell can be high enough to support the observed rates of C assimilation, without postulating transport of the species HCO 3 − or H2CO3. Calculations are presented also for alternative models in which there is membrane transport of HCO 3 − . The first includes symport of H+ with HCO 3 − , again dependent on active H+ efflux. In the second, there is active electrogenic transport of HCO 3 − . In this case the low pH in the medium outside the cell is caused by the dissociation of H2CO3 produced by hydration of CO2 which leaks from the cell cytoplasm. All three models are consistent with the observations to date, but the first is more economical of postulates. It can also explain the apparent transport of HCO 3 − by fresh-water angiosperms such asEgeria.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    The journal of membrane biology 49 (1979), S. 283-296 
    ISSN: 1432-1424
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary We have previously reported that inward positive current flows across the plasmalemma of voltage-clampedChara cells when ammonia or methylamine is added to the medium. This is attributed to (inward) uniport of the cation. We have measured the stoichiometric ratio of the quantity of methylamine transported to the quantity of positive charge transported. We find 0.9 mol/faraday from pH 5.7 to 8.5, as expected if the cation flux is much larger than that of free base. The ratio increases progressively above pH 9 as the concentration of free base becomes comparable with that of cation: the fluxes fit those predicted if neutral methylamine has a permeability of 1.8 × 10−5 m/sec. This is comparable with the permeability of the methylammonium ion, 6×10−6 m/sec, at low concentration and −200 mV, as previously reported. Low concentrations of NH 4 + are found to inhibit entry of CH3NH 3 + when membrane PD is constant. Half maximum inhibition is found at ∼20 μm NH 4 + , in agreement with the apparentK M for NH 4 + binding to its uniporter site. This suggests that NH 4 + and CH3NH 3 + enter by the same uniporter, competing for binding to its binding site.
    Type of Medium: Electronic Resource
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