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  • 1
    Schlagwort(e): Electronic books.
    Materialart: Online-Ressource
    Seiten: 1 online resource (111 pages)
    Ausgabe: 1st ed.
    ISBN: 9783800671366
    Sprache: Deutsch
    Anmerkung: Cover -- Titel -- Impressum -- Inhaltsübersicht -- Nachhaltigkeitsmanagement kompakt auf einen Blick -- Kapitel 1: 10 überzeugende Gründe für mehr Nachhaltigkeit in Unternehmen -- von Leyla Azizi, Colin Bien, Remmer Sassen, Stella-Maria Yerokhin -- Kapitel 2: Normative und regulative Anforderungen an das unternehmerische Nachhaltigkeitsmanagement im Kontext der EU-Taxonomie -- von Lisa Junge und Remmer Sassen Hintergrund Green Deal -- EU-Taxonomie: Rahmenwerk zur Klassifizierung nachhaltiger Wirtschaftsaktivitäten -- Umweltziele der EU-Taxonomie -- Technische Bewertungskriterien der EU-Taxonomie -- EU-Taxonomie in der Praxis -- Kapitel 3: Erste Schritte zur Implementierung eines Nachhaltigkeitsmanagements: Strategien und Prozesse -- von Marlen Gabriele Arnold -- Bestandaufnahme der existierenden Nachhaltigkeitsaktivitäten -- Entwicklung einer Nachhaltigkeitsstrategie -- Formulierung abgeleiteter Ziele und Maßnahmen -- Integration der Maßnahmen in betriebliche Prozesse -- Kapitel 4: Nachhaltige Unternehmenssteuerung -- von Peter Rötzel -- Zielkonsense und Zielkonflikte in der nachhaltigen Unternehmenssteuerung -- Spannungsfeld zwischen Integration in bestehende Steuerungssysteme und Nutzung von separaten Steuerungssystemen -- Nachhaltigkeitscontrolling durch Indikatoren und Kennzahlen -- Kapitel 5: Nachhaltigkeitskommunikation -- von Sarah Bärsch, Yu-Shan Lin Feuer und Remmer Sassen -- Warum sollten Unternehmen über ihre Nachhaltigkeitsaktivitäten berichten? -- Wie können Unternehmen ihre Nachhaltigkeitsleistung offenlegen und darüber berichten? -- Welche Standards und Instrumente können für die Nachhaltigkeitsberichterstattung angewandt werden? -- Was kommt zukünftig auf die Unternehmen im Bereich der Nachhaltigkeitsberichterstattung zu? -- Übersicht über die Autorinnen und Autoren -- Sachverzeichnis.
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  • 2
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Li, Sanzhong; Geldmacher, Jörg; Hauff, Folkmar; Garbe-Schönberg, Dieter; Yu, Shan; Zhao, Shujuan; Rausch, Svenja (2014): Composition and timing of carbonate vein precipitation within the igneous basement of the Early Cretaceous Shatsky Rise, NW Pacific. Marine Geology, 357, 321-333, https://doi.org/10.1016/j.margeo.2014.09.046
    Publikationsdatum: 2023-06-27
    Beschreibung: Numerous calcium carbonate veins were recovered from the igneous basement of the Early Cretaceous Shatsky Rise during Integrated Ocean Drilling Program (IODP) Expedition 324. The chemical (Sr/Ca, Mg/Ca) and isotopic (87Sr/86Sr, 143Nd/144Nd, delta18O, delta13C) compositions of these veins were determined to constrain the timing of vein formation. A dominant control by seawater chemistry on calcite composition is evident for most vein samples with variable contributions from the basaltic basement. Slightly elevated precipitation temperatures (as inferred from oxygen isotope ratios), indicative of hydrothermal vein formation, are only observed at Site U1350 in the central part of Shatsky Rise. The highest 87Sr/86Sr ratios (least basement influence) of vein samples at each drill site range from 0.70726 to 0.70755 and are believed to reflect the contemporaneous seawater composition during the time of calcite precipitation. In principle, age information can be deduced by correlating these ratios with the global seawater Sr isotope evolution. Since the Sr isotopic composition of seawater has fluctuated three times between the early and mid Cretaceous, no unambiguous precipitation ages can be constrained by this method and vein precipitation could have occurred at any time between ~ 80 and 140 Ma. However, based on combined chemical and isotopic data and correlations of vein composition with formation depth and inferred temperature, we argue for a rather early precipitation of the veins shortly after basement formation at each respective drill site.
    Schlagwort(e): 324-U1347A; 324-U1349A; 324-U1350A; Barium; Calcification temperature; Cerium; DEPTH, sediment/rock; DRILL; Drilling/drill rig; DSDP/ODP/IODP sample designation; Dysprosium; Erbium; Europium; Event label; Exp324; Gadolinium; Holmium; ICP-MS, Agilent 7500c; ICP-OES, SPECTRO Ciros CCD; Integrated Ocean Drilling Program / International Ocean Discovery Program; IODP; Joides Resolution; Lanthanum; Lead; Lithium; Lutetium; Magnesium/Calcium ratio; Manganese; Neodymium; Neodymium-143/Neodymium-144 ratio; Praseodymium; Replicates; Rubidium; Samarium; Sample code/label; Sample comment; Scandium; Shatsky Rise; Strontium; Strontium/Calcium ratio; Strontium-87/Strontium-86 ratio; Terbium; Thulium; Uranium; Ytterbium; Yttrium; δ13C; δ18O
    Materialart: Dataset
    Format: text/tab-separated-values, 636 data points
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  • 3
    Digitale Medien
    Digitale Medien
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 71 (1992), S. 3966-3974 
    ISSN: 1089-7550
    Quelle: AIP Digital Archive
    Thema: Physik
    Notizen: An increase of surface refractive index and a recovery of the r33 electro-optic coefficient have been observed for proton-exchanged LiTaO3 optical waveguides after annealing. On the basis of the results of nuclear reaction analysis, x-ray rocking curve analysis, and infrared-absorption spectroscopy, a qualitative model to explain these phenomena is proposed. The evolutions of the index profile and the r33 coefficient after proton exchange and annealing are considered to be caused by the movement of protons in the crystal lattice and the interdiffusion of protons and Li ions. The condition required for the fabrication of waveguides with good electro-optic performance is also shown.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Journal of the American Chemical Society 96 (1974), S. 1259-1260 
    ISSN: 1520-5126
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Journal of the American Chemical Society 76 (1954), S. 3367-3369 
    ISSN: 1520-5126
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Science Ltd
    Journal of neurochemistry 93 (2005), S. 0 
    ISSN: 1471-4159
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Medizin
    Notizen: The Na+, K+-ATPase or Na+, K+-pump plays a critical role in ion homeostasis and many cellular events. The Na+, K+-pump activity is regulated by serine/threonine phosphorylation, the role of tyrosine kinases in the regulation, however, is obscure. We now present novel evidence showing that tyrosine phosphorylation activates the Na+, K+-pump in cortical neurons. The electrogenic activity of the Na+, K+-pump was measured using whole-cell voltage clamp. A tonic activity was revealed by an inward current induced by the specific inhibitor ouabain or strophanthidin; an outward current due to activation of the pump was triggered by raising extracellular K+. The inward and outward currents were attenuated by the tyrosine kinase inhibitor genistein, herbimycin A, or lavendustin A, while blocking tyrosine phosphatases increased the pump current. Down-regulation of the pump current was also seen with the Src inhibitor PP1 and intracellularly applied anti-Lyn or anti-Yes antibody. Consistently, intracellular application of Lyn kinase up-regulated the pump current. Immunoprecipitation and western blotting showed tyrosine phosphorylation and a direct interaction between Lyn and the α3 subunit of the Na+, K+-pump. The tyrosine phosphorylation of the α3 subunit was reduced by serum deprivation. These data suggest that the Na+, K+-ATPase activity in central neurons is regulated by specific Src tyrosine kinases via a protein-protein mechanism and may play a role in apoptosis.
    Materialart: Digitale Medien
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  • 7
    ISSN: 1471-4159
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Medizin
    Notizen: Abstract : We studied the novel hypothesis that an upmodulation of channels for outward delayed rectifier K+ current (Iκ) plays a key role in ceramide-induced neuronal apoptosis. Exposure for 6-10 h to the membrane-permeable C2-ceramide (25 μM) or to sphingomyelinase (0.2 unit/ml), but not to the inactive ceramide analogue C2-dihydroceramide (25 μM), enhanced the whole-cell Iκ current without affecting the transient A-type K+ current and increased caspase activity, followed by neuronal apoptosis 24 h after exposure onset. Tetraethylammonium (TEA) or 4-chloro-N,N-diethyl-N-heptylbenzenebutanaminium tosylate (clofilium), at concentrations inhibiting Iκ, attenuated the C2-ceramide-induced caspase-3-like activation as well as neuronal apoptosis. Raising extracellular K+ to 25 mM similarly blocked the C2-ceramide-induced cell death ; the neuroprotection by 25 mM K+ or TEA was not eliminated by blocking voltage-gated Ca2+ channels. An inhibitor of tyrosine kinases, herbimycin A (10 nM) or lavendustin A (0.1-1 μM), suppressed Iκ enhancement and/or apoptosis induced by C2-ceramide. It is suggested that ceramide-induced Iκ current enhancement is mediated by tyrosine phosphorylation and plays a critical role in neuronal apoptosis.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Publishing Ltd
    European journal of neuroscience 9 (1997), S. 0 
    ISSN: 1460-9568
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Medizin
    Notizen: Na+-Ca2+ exchanger-associated membrane currents were studied in cultured murine neocortical neurons, using whole-cell recording combined with intracellular perfusion. A net inward current specifically associated with forward (Na+o-Ca2+i) exchange was evoked at -40 mV by switching external 140 mM Li+ to 140 mM Na+. The voltage dependence of this current was consistent with that predicted for 3Na+:1Ca2+ exchange. As expected, the current depended on internal Ca2+, and could be blocked by intracellular application of the exchanger inhibitory peptide, XIP. Raising internal Na+ from 3 to 20 mM or switching the external solution from 140 mM Li+ to 30 mM Na+ activated outward currents, consistent with reverse (Na+,-Ca2+o) exchange. An external Ca2+-sensitive current was also identified as associated with reverse Na+-Ca2+ exchange based on its internal Na+ dependence and sensitivity to XIP. Combined application of external Na+ and Ca2+ in the absence of internal Na+ triggered a 3.3–fold larger inward current than the current activated in the presence of 3 mM internal Na+, raising the intriguing possibility that Na+-Ca2+ exchangers might concurrently operate in both the forward and the reverse direction, perhaps in different subcellular locations. With this idea in mind, we examined the effect of excitotoxic glutamate receptor activation on exchanger operation. After 3–5 min of exposure to 100–200 μM glutamate, the forward exchanger current was significantly increased even when external Na+ was reduced to 100 mM, and the external Ca2+-activated reverse exchanger current was eliminated.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Publishing Ltd
    European journal of neuroscience 8 (1996), S. 0 
    ISSN: 1460-9568
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Medizin
    Notizen: Molecular cloning has revealed the existence of at least eight subtypes of metabotropic glutamate receptors (mGluRs). We examined the effect of (2S, 1′R, 2′R, 3′R)-2-(2, 3-dicarboxycyclopropyl)glycine (DCG-IV), a selective agonist of the mGluR 2/3 subtype, on excitotoxicity in mouse cortical cell cultures. Addition of DCG-IV to the exposure medium partially attenuated the rapidly triggered excitotoxic death induced by a 5 min exposure to 200 μM NMDA. This neuroprotective effect was reversed by coapplication of α-methyl-4-carboxyphenylglycine (MCPG), an antagonist of mGluRs, by pertussis toxin pretreatment and also by preincubation with dibutyryl cAMP, a stable analogue of cAMP. These results suggest that the activation of mGluR 2/3 is neuroprotective in our system. However, DCG-IV did not attenuate the slowly triggered neuronal death induced by 24 h exposure to low concentrations of NMDA, α-amino-1, 3-cyclopentanedicarboxylic acid (AMPA) or kainate. The failure of DCG-IV to block slowly triggered NMDA neurotoxicity is likely due to weak NMDA agonist activity, as demonstrated in whole-cell recording.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Journal of the American Chemical Society 99 (1977), S. 7068-7070 
    ISSN: 1520-5126
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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