ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
Collection
  • 1
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Juteau, Thierry; Eissen, Jean-Philippe; Francheteau, Jean; Needham, David; Choukroune, P; Rangin, Claude; Séguret, Marie J M; Ballard, R D; Fox, P J; Normark, William R; Carranza, A; Cordoba, D; Guerrero, J (1980): Homogeneous basalts from the East Pacific Rise at 21° N: seady state magma reservoirs at moderately fast spreading centers. Oceanologica Acta, 3(4), 487-503, https://archimer.ifremer.fr/doc/00323/43430/
    Publication Date: 2023-08-28
    Description: Forty basaltic rocks collected by submersible during the Cyamex expedition (1978) on the East PacifIc Rise at 21°N, a moderately fast spreading segment (6 cm/year opening rate) of the mid-ocean ridge, consist of angular pillow fragments and glass buds, sheet-flow slabs and samples of columnar pillars standing in collapsed fossillava pools. Most of the rocks are from the crestal are a of the Rise. The collection shows a striking petrographic homogeneity wh en compared with the range of basalts found on other segments of midocean ridges: olivine-phyric, or highly plagioclase-phyric rocks, so common in the slowspreading Famous are a in the Atlantic, are absent. All samples are typical lowpotassium oceanic tholeiites with a limited fractionation trend. Pillow-lavas, thin and thick sheet-flows cannot be distinguished by their major element compositions, as in the Galapagos rift which has the same spreading rate as the EPR at 21°N. Further, ferrobasalts have been described from the Galapagos rift, but do not appear in the Cyamex rocks. In the Cyamex area, olivine and plagioclase are the main silicate phases, and clinopyroxene is absent. In the pillows and sheet-flow samples, four generations of olivine and plagioclase crystals are distinguished. Samples from the fossillava pools are aphyric. The corresponding magma batches are presumed to have migrated rapidly through the magma chamber, and to have been extruded in large volumes, possibly during episodes ofhigh instantaneous opening rate. Fe-Ni and Fe-Cu-rich sulphide phases are common in an lava types as massive globules scatterred through the glass, or as microglobules decorating the walls of empty vesicles. Palagonite and Fe-Mn oxide thicknesses across the strike of the Rise indicate relative ages compatible with successive extrusions at the Rise axis.
    Keywords: CY-78-07-12D; CY-78-10-17D; CY-78-10-18D; CY-78-11-26D; CY-78-12-35D; CY-78-13-42D; CY-78-13-43D; CY-78-13-44D; CY-78-15-55D; CY-78-15-56D; CY-78-16-57D; CY-78-16-58D; CY-78-17-60D; CY-78-17-61D; CY-78-18-63D; CY-78-18-65D; CY-78-18-66D; CY-78-19-69D; CY-78-20-76D; CYAMEX; Cyana (Submersible); Deposit type; DEPTH, sediment/rock; Description; East Pacific Rise; Elevation of event; Event label; Identification; Latitude of event; Longitude of event; NOAA and MMS Marine Minerals Geochemical Database; NOAA-MMS; Percentage; Position; ROBA; Robotic arm; Sediment type; Substrate type; Visual description
    Type: Dataset
    Format: text/tab-separated-values, 108 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 49 (1993), S. 329-331 
    ISSN: 1420-9071
    Keywords: Pineal ; thyroxine ; deiodinase ; phenylephrine ; isoproterenol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract In the present study we show, for the first time, that phenylephrine (PHE), an α-adrenergic receptor agonist, potentiates the effect of isoproterenol (ISO), a β-adrenergic agonist, in activating pineal type II5′-deiodinase (5′-D) activity. The potentiating effect of PHE was observed only at doses of ISO which induce submaximal activation of the enzyme. However, at doses which lead to maximal activation of the enzyme, PHE was ineffective. The results suggest that not only β-, but also α-adrenergic receptors, are involved in the sympathetic noradrenergic regulation of pineal 5′-D activity in the adult rat.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 53 (1997), S. 697-699 
    ISSN: 1420-9071
    Keywords: Key words. Thymus; thyroxine; deiodinase; continuous light; isoproterenol.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. In the present study we show that thymus type II thyroxine deiodinase activity exhibits a nyctohemeral profile, with basal values during the day and high values at night. This rhythmic character is dependent on neuroadrenergic input since exposure to continuous light at night completely abolished the nocturnal rise of the enzyme activity. However, treatment with isoproterenol under light exposure at night restored it.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Springer
    The journal of membrane biology 84 (1985), S. 229-238 
    ISSN: 1432-1424
    Keywords: alcohols ; isomerism ; nervous block ; anaesthesia ; cut-off effect ; bromoalkanes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary The potency to block nervous impulse of members of normal aliphatic homologous series of primary and secondary isomers of functional derivatives of alkanes was tested in bundles of a few axons from sciatic nerves of the toadBufo marinus. For the primary substituted functional derivates of pentane, the relative potency series was 1〉H≈Br〉Cl〉COOCH3〉F〉CH2OH〉COCH3〉OH≈NH2〉COOH. For the homologous series of primary alkanols, and from saturated Ringer's solutions, the time required to reversibly reduce the amplitude of the action potential to one-half its initial value were determined. The cut-off effect was detected at the level of dodecan-1-ol, while for the primary bromoalkanes it was bromooctane. However, solutions of the secondary isomer of the inactive primary homologues, such as tridecan-5-ol and tridecan-7-ol or 2-bromononane, were able to block nervous impulse conduction reversibly. From the concentration required for an equipotent effect it was calculated that the standard free energy for adsorption of primary alkanols was −705 cal mol− CH2. Similarly, for primary bromoalkanes a value of −733 cal mol−1 CH2 was obtained. The concentration required for an equipotent effect for primary isomer (either of alkanols or bromoalkanes) is lower than those obtained for the secondary isomers. Therefore, the latter are less potent than the former. Among secondary isomers the potency decreases as the functional group is moved away from the terminal carbon. The differential effect of structural isomers of long-chain alkane derivates around the point of cut-off cannot be explained in terms of differences in chemical properties, concentration in aqueous and membrane phases, or mean molecular volume. It is concluded that a volume related to that of the hydrophobic region of the agent and not its mean molecular volume should be responsible for an expansion of the target region.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    Journal of Mathematical Physics 41 (2000), S. 6747-6765 
    ISSN: 1089-7658
    Source: AIP Digital Archive
    Topics: Mathematics , Physics
    Notes: We provide an explicit construction of quasi-invariant measures on polarized coadjoint orbits of a Lie group G. The use of specific (trivial) central extensions of G by the multiplicative group R+ allows us to restore the strict invariance of the measures and, accordingly, the unitarity of the quantization of coadjoint orbits. As an example, the representations of SL(2,R) are recovered. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Structural Biology 108 (1992), S. 269-276 
    ISSN: 1047-8477
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 99 (1995), S. 4929-4934 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Autonomic & autacoid pharmacology 25 (2005), S. 0 
    ISSN: 1474-8673
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Chemistry and Pharmacology , Medicine
    Notes: 1 The effect of WAY 405 ((R)-N-(2-methyl-(4-indolyl-1-piperazinyl)ethyl)-N-(2-pyridinyl) cyclohexane carboxamide), a putative 5-HT1A receptor antagonist, on cardiovascular function was studied. 2 In anaesthetized rats, the i.v. injection of WAY 405 did not significantly modify basal heart rate nor blood pressure at doses of 1, 3, 10 and 30 μg kg−1; while the antagonist dose dependently antagonized the 5-HT1A receptor agonist, 8-OH-DPAT (8-hydroxy-2-(di-n-propylamino)tetralin)-induced hypotension and bradycardia. 3 WAY 405 antagonized noradrenaline-induced contraction in isolated arteries, with pKB values of 6.6 ± 0.1, 6.5 ± 0.1 and 6.5 ± 0.1, for rat tail artery (α1A-adrenoceptors), rabbit aorta (α1B-adrenoceptors), and rat aorta (α1D-adrenoceptors) respectively. 4 The results show that in the control of blood pressure the new compound, WAY 405, behaves as a silent 5-HT1A receptor antagonist in the anaesthetized rat, also having low affinity for vascular α1-adrenoceptors.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    ISSN: 1474-8673
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Chemistry and Pharmacology , Medicine
    Notes: 1 The effect of WAY100635 (N-[2-[4-(2-methoxyphenyl)-1-piperazinyl]ethyl]-N-(2-pyridinyl) cyclohexanecarboxamide trihydrochloride), a 5-HT1A receptor antagonist, on cardiovascular function was studied. 2 The i.v. injection of WAY100635 dose-dependently decreased blood pressure in anaesthetized rats; while in pithed rats WAY100635 (1 mg  kg−1) displaced the phenylephrine pressor effect. 3 WAY100635 antagonized phenylephrine-induced contraction in rabbit and rat aorta (pA2 of 6.88 and 7.93 and Schild slopes of −0.83 and −1.21, respectively); while in rat caudal artery pKB was 7.45 and the Schild slope of −0.56, suggesting a complex interaction in this vessel. 4 The results show that WAY100635 induced hypotension in the anaesthetized rat and suggest that this effect could be partially explained by antagonism of vascular α1-adrenoceptors.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Autonomic & autacoid pharmacology 25 (2005), S. 0 
    ISSN: 1474-8673
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Chemistry and Pharmacology , Medicine
    Notes: 1 The pressor action of noradrenaline and its blockade by selective α1-adrenoceptor antagonists in the pithed mouse were evaluated. 2 Chloroethylclonidine (α1B/D-adrenoceptor alkylating agent) or BMY 7378 (α1D-adrenoceptor antagonist), both at 1 mg kg−1, did not block the increase in blood pressure induced by noradrenaline. 3 5-Methylurapidil (α1A-adrenoceptor antagonist), at 0.1 mg kg−1, displaced the dose–response curve approximately six-fold to the right. 4 The results support the idea that the pithed mouse vasculature express α1A-adrenoceptors and suggest that it is a good model to study the roles of α1-adrenoceptors in gene knockout or overexpression.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...