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  • 1
    ISSN: 1572-8838
    Keywords: ball milling ; chlorate electrolysis ; electrocatalysis ; hydrogen evolution ; nanocrystalline
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Notes: Abstract Electrodes made from nanocrystalline Ti:Ru:Fe (2−y:1+y/2:1+y/2), with y varying from 0 to 1 by step of 0.25, and Ti:Ru:Fe:O (2:1:1:w), with w varying from 0 to 2 by step of 0.5, were prepared and tested as activated cathodes for the hydrogen evolution reaction in typical chlorate electrolysis conditions. These electrodes were subjected to an accelerated aging test, consisting of a succession of cycles of hydrogen discharge (HER) and open-circuit (OCP) conditions. In addition to monitoring the cathodic overpotential value during the aging test, visual inspection and mass loss measurements were performed on the electrodes at the end of the test to assess their stability. In the case of Ti:Ru:Fe (2:1:1), a large increase of the cathodic overpotential value is observed after 20 cycles. Adding O to the formulation causes a remarkable improvement of the long-term stability of the electrodes. As little as [O] = 10 at.% in nanocrystalline Ti:Ru:Fe:O (2:1:1:w) materials is sufficient for the electrode to show absolutely no sign of degradation after 50 cycles of HER/OCP, the longest accelerated test conducted. Adding more O to the formulation of the material does not lead to further stability improvement. A better stability under the conditions of the accelerated aging test can also be observed for nanocrystalline Ti:Ru:Fe (2−y:1+y/2:1+y/2) materials with y 〉 0. In that case however, the level of improvement is dependent on the value of y. The best results are obtained for y = 0.75. A hypothesis is proposed to explain the improved stability obtained by lowering the Ti content and/or by adding O. The similarity and difference between both ways of improving the stability of the nanocrystalline Ti:Ru:Fe materials are also discussed.
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  • 2
    ISSN: 1572-879X
    Keywords: supported catalyst ; nanocrystalline alloys ; metastable alloys ; ball milling ; mechanical alloying ; surface
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The high energy ball-milling technique has been used to produce metastable Ni(Ru) alloys supported on alumina. This catalyst has potential application for the hydrogenation of the C=O bond. The active species are first formed by mechanical alloying pure Ni and Ru powders. The alumina support is ground independently until no structural transformation occurs. Finally, the supersaturated Ni(Ru) powder is milled with the alumina support to produce highly dispersed individual Ni(Ru) nanocrystals on the surface of Al2O3. This supported catalyst has been characterized by X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy and thermal desorption spectroscopy.
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  • 3
    ISSN: 1432-0878
    Keywords: Key words Teleost fish ; Puberty ; Testes ; Sex steroids ; Ultrastructure ; Steroidogenesis ; Clarias gariepinus (Teleostei)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract  The present report focuses on the mechanism(s) involved in the steroid-induced decrease of androgen production in immature African catfish testes that was observed in previous studies. Juvenile animals were implanted with Silastic pellets containing different 11-oxygenated androgens (11-ketotestosterone, KT; 11β- hydroxyandrostenedione, OHA; 11-ketoandrostenedione, KA), testosterone (T) or estradiol-17β (E2). Control groups received steroid-free pellets. Two weeks later, testis tissue fragments were either incubated with increasing concentrations of catfish luteinizing hormone (LH), or incubated with [3H]-pregnenolone ([3H]-P5) or [3H]-androstenedione ([3H]-A). Tissue fragments were also prepared for the quantitative assessment of Leydig cell morphology. Most of the parameters studied were not affected significantly by implantation of E2. Implantation of all androgens inhibited both the basal and the LH-stimulated androgen secretory capacity in vitro. This was associated with a reduced size of the Leydig cells and loss of half of their mitochondria. The studies on the metabolism of tritiated steroid hormones indicated that steroidogenic steps prior to 11β-hydroxylation, probably C17–20 lyase activity, were affected by all androgens. Although the effects of 11-oxygenated androgens and T on Leydig cells were mostly similar, previous work showed that only the 11-oxygenated androgens stimulated spermatogenesis, suggesting that distinct mechanisms of action are used by 11-oxygenated androgens and T. These mechanisms, however, seem to merge on the same target(s) to impair Leydig cell androgen production. Such a negative feedback mechanism may be of relevance in the context of the decline in androgen secretion per milligram testis tissue that accompanies the first wave of spermatogenesis in pubertal African catfish.
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  • 4
    ISSN: 1432-136X
    Keywords: Sex steroids ; Blood levels ; Testicular in vitro secretion ; Pubertal development ; African catfish (Clarias gariepinus)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Blood serum and testicular tissue samples were collected from 3 to 13-month-old African catfish (groups A-G) in order to study their pubertal development. The sampling covered the period from before the beginning of spermatogenesis until full maturity. Testes of fish in group A contained spermatogonia alone. In testes of group B, spermatogonia, spermatocytes and spermatids were present. Spermatozoa were first observed in group C and became predominant as the fish attained full maturity (group G). Several sex steroids were determined in the blood samples. Testosterone was the quantitatively dominating androgen in the blood serum (3–5 ng·ml-1) in groups B and C (fish in group A were too small to collect blood samples). In group D, the concentrations of 11-ketotestosterone and 11β-hydroxyandrostenedione increased to levels similar to those of testosterone. Androstenedione that was undetectable before (below 0.4 ng·ml serum-1), also increased to 3–5 ng·ml-1 in group D. The levels of androgens kept increasing until the fish attained full maturity (group G). In order to monitor the responsiveness to gonadotropic hormone and the steroid secretion capacity, the in vitro secretion of two steroids (11β-hydroxyandrostenedione and 17α,20β-dihydroxy-4-pregnen-3-one) by testicular tissue was quantified at the different stages of development. Testicular maturation was accompanied by changes of both the steroid secretion capacities and of the sensitivity to gonadotropic hormone. The most important changes occurred just after the initiation of spermatogenesis, as spermatocyte/spermatid formation was associated with a drop of the secretory capacity (amount of steroid secreted per milligram of tissue incubated) and with a reduced sensitivity to gonadotropic hormone. At later stages, when the testicular weight substantially increased concurrently with the formation of numerous spermatozoa, both the secretory capacity and the responsiveness to gonadotropic hormone increased again to reach the levels typical of adult fish. The blood levels of androgens appeared to be positively related to the increasing testicular weight in the later phases of development.
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  • 5
    ISSN: 1432-136X
    Keywords: Gonadotropic hormone ; Sex steroids ; Reproductive cycle ; Testis ; Rainbow trout, Oncorhynchus mykiss
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Male rainbow trout were treated with salmon gonadotropic hormone (GTH) at different stages of the circannual reproductive cycle; spawning fish were also treated with an antiserum against salmon GTH. Injection of GTH led to a several-fold increase of plasma sex steroid levels during spermatogenesis and in the spawning season but was without effect at early stages of testicular development. GTH neutralization during the spawning season was followed by a several-fold decrease of plasma sex steroid levels. During spermatogenesis and in the spawning season, both treatment regimes resulted in an increased sensitivity of testicular explants in response to a subsequent stimulation of steroid secretion in vitro. This up-regulatory response may facilitate and maintain the high sex steroid plasma levels observed during the spawning season. It may also be necessary to allow for concomitant peak values of plasma GTH and sex steroids in the spawning season, a situation difficult to understand within the negative feedback concept. The adaptive capacities of the testicular steroidogenic system indicate that it is not only an effector site for GTH but also an active part of the endocrine system controling reproduction.
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