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    Publication Date: 2011-04-01
    Print ISSN: 0017-9310
    Electronic ISSN: 1879-2189
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Published by Elsevier
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  • 3
    Publication Date: 2017-08-08
    Description: The continental slope of the northern Gulf of Mexico seaward of the Mississippi Delta is characterized by very rapid Quaternary sedimentation. Thick sequences of underconsolidated muds and mudstones are present, which are severely overpressured. In the Ursa Basin, Site U1322 of the Integrated Ocean Drilling Program (IODP) provided an excellent coring record of interleaved fine-grained turbidites and hemipelagic sediments, in part severely affected by submarine slumping and sliding after deposition. Cores were continuously sampled and analyzed for anisotropy of magnetic susceptibility (AMS), to elucidate the effects of different transport mechanisms and degree of settling and consolidation on magnetic fabric properties. Generally AMS ellipticity increases with depth irrespective of transport mode, due to loss of porosity. Samples from slumped mass transport deposits (MTD), however, have higher AMS if compared to immediately overlying non-slumped material. MTD samples dominantly show triaxial magnetic fabrics whereas those found in non-slumped sediments are much more oblate. Long axes of the fabric ellipsoid reflect the direction of eastward to southward suspension transport in samples not overprinted by sliding or slumping. Short ellipsoid axes in non-slumped material are vertical, and thus parallel to the axis of maximum uniaxial shortening. In the MTD samples, many short ellipsoid axes are inclined, reflecting an overprint of the uniaxial shortening by bed-parallel shearing induced by the slumping. Shear and MTD transport direction deduced from the fabrics is top-to-SE, downslope along the morphological axis of Ursa Basin. Generally we show that magnetic fabrics of muds and mudstones are sensitive recorders of sedimentary and tectonic processes, and can be used to reconstruct essential parts of basin history.
    Type: Article , PeerReviewed
    Format: text
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 163 (1988), S. 609-620 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary In conventional two microelectrode experiments, acetylcholine had qualitatively the same effect as GABA and glutamate on membrane potential and input resistance of muscle fibres of the opener and intrinsic stomach muscles of crayfish (Austropotamobius torrentium). In patch-clamp experiments, acetylcholine occasionally elicited single channel openings in cell-attached patches on these muscles. If outside-out patches were excised and the Cl− concentration was high on both sides of the membrane, acetylcholine at concentrations of 1 nM regularly elicited single channel currents. The amplitude of single channel currents depended strongly on the intracellular concentration of Cl−. The reversal potential of the channel, determined after replacing intracellular K+ with Cs+, corresponded to the Nernst potential for Cl−. The voltage dependence and the reversal potential of single channel current amplitudes elicited by ACh, glutamate and GABA were identical. The distribution of life times of openings (〉1 ms) elicited by ACh and glutamate could be fitted by a single exponential with a time constant of about 2.5 ms, corresponding to the mean open time. ACh and glutamate applied to the same outside-out patch showed cross-desensitization, and thus ACh and glutamate activate the same channels. An excitatory, cationic ACh-activated channel could not be identified. Permeabilities of the chloride channel were calculated according to the Goldman-Hodgkin-Katz equation at different membrane potentials. Negative single channel current amplitudes (inward currents) could be fitted with a permeability ofπ 2= 3.9×10−14 cm3s−1. For positive currents (outward) the channel had a permeability ofπ 1= 1.4× 10−14 cm3s−1. The permeability of the channel declined from 16×10−14 cm3s−1 to 2.3×10−14 cm3s−1 if the intracellular Cl−-concentration was raised from 6 to 257 mM. The activation elicited by acetylcholine was inhibited by extracellular Ca++. The mean current activated by ACh was reduced by a factor of 50 if the extracellular concentration of Ca++ was raised from 0.1 mM to the physiological concentration of 13.5 mM.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Glutamate activated, excitatory single channel currents were recorded from 5 different muscles of crayfish (Austropotamobius torrentium) from abdomen, legs and stomach. Cell-attached and outside-out excised membrane patches with GΩ-seals were studied. At −70 mV membrane potential and 19 °C, single channel currents activated by 0.5 mM glutamate had an amplitude of −7.6 pA, a mean open time of 0.22 ms and a mean burst length of 0.58 ms. These values did not show significant differences in all muscles investigated. The distributions of open times and of burst durations were described by single exponentials. The distributions of closed times could be fitted only by at least two exponentials. The short component of on average 0.1 ms represented closings within bursts, a longer component of on average 0.9 ms grouping of bursts. Burst durations (but not individual open times) increased with rising glutamate concentration: the relative open time of the channel was approximately proportional to glutamate concentration between 0.1 and 5 mM. The channels described above could not be activated by the glutamate analogues kainate and NMDA, but were about 10 times more sensitive to quisqualate than to glutamate. Quisqualate elicited single channel currents of the same amplitude as those triggered by glutamate. Compared at the same concentrations, channel open times and burst durations were about 4 times longer in quisqualate than in glutamate. A model describing the kinetics of the glutamate-activated excitatory channels is discussed. In addition, a type of Ca-independent, depolarization-activated K+-channel is reported.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 159 (1986), S. 591-609 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Outside-out and inside-out patches of membrane were excised from different muscles of crayfish (Austropotamobius torrentium) and single channel currents elicited by synaptic transmitters and their analogues were measured with the patchclamp technique. If the Cl−-concentration was high on both sides of the membrane, glutamate even at concentrations 〈1 μM elicited low amplitude single channel currents, which were identified to be Cl−-currents. The same channels were also activated by 10 μM GABA. Glutamate and GABA showed competition in activating these inhibitory channels. Amplitude histograms of the single channel currents presented well defined peaks corresponding to 3 channel substatesI 1,I 2 andI 3, with conductances of aboutγ(I1)=22 pS in high chloride corresponding to a permeabilityπ Cl(I1)=3.5× 10−14 cm3/s),γ(I2)=2γ(I1) andγ(I3)=3γ(I1). Glutamate activated preferably stateI 1, and GABA stateI 2, but both could activate all states at sufficient concentration. Distributions of the open times in the different states were plotted and could be fitted each with one or two exponentials described by time constants ofτ(I1) of 1 and 6 ms,τ(I2) of 2 to 3 ms, andτ(I3) or 1 to 2 ms. The burst durations had components of 3 to 4 and of 30 to 40 ms. All these durations were approximately the same when the channels were activated by glutamate and GABA. The analogue quisqualate of glutamate, as well as the GABA analogueβ-guanidino propionic acid also elicited the respective patterns of states of the inhibitory channel. Quisqualate is by far the most effective agonist and glutamate is more effective than GABA at the inhibitory receptor. Picrotoxin blocked activation of the inhibitory channel by GABA more effectively than by glutamate. The importance of the activation of the inhibitory channel by glutamate as well as by GABA and their analogues is discussed. Elements of a tentative reaction schema are proposed.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 166 (1990), S. 757-768 
    ISSN: 1432-1351
    Keywords: Synaptic transmission ; Glutamate ; Pulse ; application of drug ; Cationic channels ; Desensitization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Outside-out patches from membrane of muscles of crayfish (Austropotamobius torrentium) were excised, and L-glutamate (glu) was applied to these patches in pulses of different duration, performing a concentration step within about 0.2 ms. While a uniform population of cationic channels is seen in equilibrium applications of glu, four kinetically different channel types were revealed by the pulse applications of glu. All these channel types had the same single channel conductance and durations of elementary short single channel openings and closings, and they thus form a family of channels. Type I, incompletely desensitizing channels reacted to a pulse of 10 mM glu with a peak open probability of 0.7 within 0.3 ms. Thereafter open probability decayed with a time constant of desensitization of about 5 ms, reaching a plateau of about 1/20 peak probability which was maintained as long as 10 mM glu were present. The peak probabilities of channel opening were proportional to approximately power 2.5 of the glu concentration, for low concentrations. Type II, completely desensitizing channels also were activated very rapidly by glu pulses, but their time constant of desensitization was 1–2 ms, and no channel openings were observed after more than 10 ms presence of a high glu concentration. The peak probabilities of channel opening rose with about the 5th power of glu concentration (for low concentrations). Type III, non-desensitizing channels, were observed relatively rarely. They were activated much more slowly and reached much lower probabilities of opening than type I and II channels. They did not show appreciable desensitization. Type IV, short-opening channels, develop sometimes from type I channels while recording, and may revert to the type I. Type IV channels show an additional open time component of 0.08 ms average duration, and a relatively long additional closed time of on average 1.3 ms. In addition to channel measurements, distributions of amplitudes and time courses of macroscopic quantal currents were determined. It is discussed in which way the different channel types may contribute to the quantal currents.
    Type of Medium: Electronic Resource
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