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  • 1
    Publication Date: 2016-08-04
    Description: Long-Term Socio-Ecological Research (LTSER) is an inter- and transdisciplinary research field addressing socio-ecological change over time at various spatial and temporal scales. In the Austrian Eisenwurzen region, an LTSER platform was founded in 2004. It has fostered and documented research projects aiming at advancing LTSER scientifically and at providing regional stakeholders with relevant information for sustainable regional development. Since its establishment, a broad range of research activities has been pursued in the region, integrating information from long-term ecological monitoring sites with approaches from social sciences and the humanities, and in cooperation with regional stakeholders. Based on the experiences gained in the Eisenwurzen LTSER platform, this article presents current activities in the heterogeneous field of LTSER, identifying specific (inter-)disciplinary contributions of three research strands of LTSER: long-term ecological research, socio-ecological basic research, and transdisciplinary research. Given the broad array of diverse contributions to LTSER, we argue that the platform has become a relevant “boundary organization,” linking research to its regional non-academic context, and ensuring interdisciplinary exchange among the variety of disciplines. We consider the diversity of LTSER approaches an important resource for future research. Major success criteria of LTSER face specific challenges: (1) existing loose, yet stable networks need to be maintained and extended; (2) continuous generation of and access to relevant data needs to be secured and more data need to be included; and (3) consecutive research projects that have allowed for capacity building in the past may be threatened in the future if national Austrian research funders cease to provide resources.
    Electronic ISSN: 2071-1050
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Published by MDPI Publishing
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 112 (1979), S. 781-792 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Heterocyclic Seven-membered Ring Compounds, XXII. Synthesis and Thermolysis of Substituted 4-Phenyl-l -benzothiepin 1-Oxides4-Phenyl-l-benzothiepin l-oxides 3a and b have been prepared as well via the benzothiepinone 1-oxide 2 as by direct oxidation of the parent 1-benzothiepins 6a and b. The synthesis of 3c and d was only accomplished by the second way. Further oxidation of 3a-d yielded the thermally stable dioxides 4a-d. Thermolysis of 3a-d produced the corresponding naphthalenes 5a-d by elimination of SO. The rates of the reaction 3→5 have been estimated for one temperature each.
    Notes: Die 4-Phenyl-l-benzothiepin-l-oxide 3a und b wurden sowohl über das Benzothiepinon-1-oxid 2 als auch durch direkte Oxidation der entsprechenden 4-Phenyl- 1-benzothiepine 6a und b dargestellt. Die Synthese von 3c und d erfolgte nur auf dem zweiten Weg. Weiteroxidation von 3a-d führte zu den thermisch stabilen Dioxiden 4a-d. Die Thermolyse von 3a-d lieferte unter Abspaltung von SO die entsprechenden Naphthaline 5a-d. Die Geschwindigkeitskonstanten der Reaktion 3→5 wurden für je eine Temperatur bestimmt.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1977 (1977), S. 1874-1887 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Heterocyclic Seven-Membered Ring Compounds, XXI. - Photochemical Reactions of Substituted 4-Phenyl-1-benzothiepinsOn photoisomerization substituted 4-phenyl-1-benzothiepins 2a-d undergo ring closure to give the expected 1-phenyl-2a,7b-dihydrocyclobuta[b][1]benzothiophenes 4a-d which are then transformed into the corresponding 2a-phenyl-2a,7b-dihydrocyclobuta[b][1]benzothiophenes 5a-d in a second photoreaction.
    Notes: Die Photoisomerisierung der substituierten 4-Phenyl-1-benzothiepine 2a-d liefert zunächst unter Ringschluß die erwarteten 1-Phenyl-2a,7b-dihydrocyclobuta[b][1]benzothiophene 4a-d. Diese werden in einer nachfolgenden Photoumlagerung in die entsprechenden 2a-Phenyl-2a,7b-dihydrocyclobuta[b][1]benzothiophene 5a-d übergeführt.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 87 (1975), S. 843-844 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 14 (1975), S. 812-813 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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