TY - THES A1 - Wolf, Mathias Johannes T1 - The role of partial melting on trace element and isotope systematics of granitic melts T1 - Die Bedeutung partieller Schmelzbildung für die Spurenelement- und Isotopensystematik granitischer Schmelzen N2 - Partial melting is a first order process for the chemical differentiation of the crust (Vielzeuf et al., 1990). Redistribution of chemical elements during melt generation crucially influences the composition of the lower and upper crust and provides a mechanism to concentrate and transport chemical elements that may also be of economic interest. Understanding of the diverse processes and their controlling factors is therefore not only of scientific interest but also of high economic importance to cover the demand for rare metals. The redistribution of major and trace elements during partial melting represents a central step for the understanding how granite-bound mineralization develops (Hedenquist and Lowenstern, 1994). The partial melt generation and mobilization of ore elements (e.g. Sn, W, Nb, Ta) into the melt depends on the composition of the sedimentary source and melting conditions. Distinct source rocks have different compositions reflecting their deposition and alteration histories. This specific chemical “memory” results in different mineral assemblages and melting reactions for different protolith compositions during prograde metamorphism (Brown and Fyfe, 1970; Thompson, 1982; Vielzeuf and Holloway, 1988). These factors do not only exert an important influence on the distribution of chemical elements during melt generation, they also influence the volume of melt that is produced, extraction of the melt from its source, and its ascent through the crust (Le Breton and Thompson, 1988). On a larger scale, protolith distribution and chemical alteration (weathering), prograde metamorphism with partial melting, melt extraction, and granite emplacement are ultimately depending on a (plate-)tectonic control (Romer and Kroner, 2016). Comprehension of the individual stages and their interaction is crucial in understanding how granite-related mineralization forms, thereby allowing estimation of the mineralization potential of certain areas. Partial melting also influences the isotope systematics of melt and restite. Radiogenic and stable isotopes of magmatic rocks are commonly used to trace back the source of intrusions or to quantify mixing of magmas from different sources with distinct isotopic signatures (DePaolo and Wasserburg, 1979; Lesher, 1990; Chappell, 1996). These applications are based on the fundamental requirement that the isotopic signature in the melt reflects that of the bulk source from which it is derived. Different minerals in a protolith may have isotopic compositions of radiogenic isotopes that deviate from their whole rock signature (Ayres and Harris, 1997; Knesel and Davidson, 2002). In particular, old minerals with a distinct parent-to-daughter (P/D) ratio are expected to have a specific radiogenic isotope signature. As the partial melting reaction only involves selective phases in a protolith, the isotopic signature of the melt reflects that of the minerals involved in the melting reaction and, therefore, should be different from the bulk source signature. Similar considerations hold true for stable isotopes. N2 - Partielle Schmelzbildung ist ein zentraler Prozess für die geochemische Differentiation der Erdkruste (Vielzeuf et al., 1990). Die Umverteilung chemischer Elemente während der Schmelzbildung beeinflusst die Zusammensetzung der oberen und unteren Erdkruste entscheidend und stellt einen Mechanismus zur Konzentration und zum Transport chemischer Elemente dar. Das Verständnis der diversen Prozesse und der kontrollierenden Faktoren ist deshalb nicht nur von wissenschaftlichem Interesse sondern auch von ökonomischer Bedeutung um die Nachfrage für seltene Metalle zu decken. Die Umverteilung von Haupt- und Spurenelementen während des partiellen Aufschmelzens ist ein entscheidender Schritt für das Verständnis wie sich granitgebundene Lagerstätten bilden (Hedenquist and Lowenstern, 1994). Die Schmelzbildung und die Mobilisierung von Erz-Elementen (z. B. Sn, W, Nb, Ta) in die Schmelze hängt von der Zusammensetzung der sedimentären Ausgangsgesteine und den Schmelzbedingungen ab. Verschiedene Ausgangsgesteine haben aufgrund ihrer Ablagerungs- und Verwitterungsgeschichte unterschiedliche Zusammensetzungen. Dieses spezifische geochemische „Gedächtnis“ resultiert in unterschiedlichen Mineralparagenesen und Schmelzreaktionen in verschiedenen Ausgangsgesteinen während der prograden Metamorphose. (Brown and Fyfe, 1970; Thompson, 1982; Vielzeuf and Holloway, 1988). Diese Faktoren haben nicht nur einen wichtigen Einfluss auf die Verteilung chemischer Elemente während der Schmelzbildung, sie beeinflussen auch das Volumen an Schmelze, die Extraktion der Schmelze aus dem Ausgangsgestein und deren Aufstieg durch die Erdkruste (Le Breton and Thompson, 1988). Auf einer grösseren Skala unterliegen die Verteilung der Ausgangsgesteine und deren chemische Alteration (Verwitterung), die prograde Metamorphose mit partieller Schmelzbildung, Schmelzextraktion und die Platznahme granitischer Intrusionen einer plattentektonischen Kontrolle. Das Verständnis der einzelnen Schritte und deren Wechselwirkungen ist entscheidend um zu verstehen wie granitgebunden Lagerstätten entstehen und erlaubt es, das Mineralisierungspotential bestimmter Gebiete abzuschätzen. Partielles Aufschmelzen beeinflusst auch die Isotopensystematik der Schmelze und des Restites. Die Zusammensetzungen radiogener und stabiler Isotopen von magmatischen Gesteinen werden im Allgemeinen dazu verwendet um deren Ursprungsgesteine zu identifizieren oder um Mischungsprozesses von Magmen unterschiedlichen Ursprunges zu quantifizieren (DePaolo and Wasserburg, 1979; Lesher, 1990; Chappell, 1996). Diese Anwendungen basieren auf der fundamentalen Annahme, dass die Isotopenzusammensetzung der Schmelze derjenigen des Ausgangsgesteines entspricht. Unterschiedliche Minerale in einem Gestein können unterschiedliche, vom Gesamtgestein abweichende, Isotopenzusammensetzungen haben (Ayres and Harris, 1997; Knesel and Davidson, 2002). Insbesondere für alte Minerale, mit einem unterschiedlichen Mutter-Tochter Nuklidverhältnis, ist eine spezifische Isotopenzusammensetzung zu erwarten. Da im partiellen Schmelzprozess nur bestimmte Minerale eines Gesteines involviert sind, entspricht die Isotopenzusammensetzung der Schmelze derjenigen der Minerale welche an der Schmelzreaktion teilnehmen. Daher sollte die Isotopenzusammensetzung der Schmelze von derjenigen des Ursprungsgesteines abweichen. Ähnliche Überlegungen treffen auch für stabile Isotopen zu. KW - geochemistry KW - trace elements KW - radiogenic isotopes KW - stable isotopes KW - resources KW - Sn Y1 - 2019 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-423702 ER - TY - CHAP A1 - Thorau, Christian T1 - "What ought to be heard" : touristic listening and the guided ear T2 - The Oxford handbook of music listening in the 19th and 20th centuries Y1 - 2019 SN - 978-0-19-046696-1 SP - 207 EP - 227 PB - Oxford University Press CY - New York ER - TY - BOOK ED - Thorau, Christian ED - Ziemer, Hansjacob T1 - The Oxford handbook of music listening in the 19th and 20th centuries N2 - An idealized image of European concert-goers has long prevailed in historical overviews of the nineteenth and twentieth centuries. This act of listening was considered to be an invisible and amorphous phenomenon, a naturally given mode of perception. This narrative influenced the conditions of listening from the selection of repertoire to the construction of concert halls and programmes. However, as listening moved from the concert hall to the opera house, street music, and jazz venues, new and visceral listening traditions evolved. In turn, the art of listening was shaped by phenomena of the modern era including media innovation and commercialization. This Handbook asks whether, how, and why practices of music listening changed as the audience moved from pleasure gardens and concert venues in the eighteenth century to living rooms in the twentieth century, and mobile devices in the twenty-first. Through these questions, chapters enable a differently conceived history of listening and offer an agenda for future research. Y1 - 2019 SN - 978-0-19-046696-1 PB - Oxford University Press CY - New York ER - TY - RPRT A1 - Roggeband, Conny T1 - International women’s rights BT - Progress under attack? T2 - KFG Working Paper Series N2 - This paper explores current contestations of women’s rights and the implications thereof for international legislation. While contestation over women’s rights is a far from new phenomenon, over the past two decades opposition to gender equality has become better organized at the transnational level, mobilizing a dispersed set of state and non-state actors, and is becoming more successful in halting the progress of women’s rights. I argue that the position of oppositional actors vis-à-vis women rights activism appears to be strengthened by two recent political developments: democratic backsliding and the closure of civic space. Some preliminary findings show how these interrelated developments lead to an erosion of women’s rights at the national level. Governments use low key tactics to dismantle institutional and implementation arrangements and sideline women’s organisations. Next, I explore the implications of these developments for gender equality norms at the national and international level. The active strategy of counter norming adopted by conservative and religious state and non-state actors, designed to circumvent and also undermine Western norms, is increasingly successful. In addition to this, the threatened position of domestic actors monitoring compliance of international treaties, makes the chances of backsliding on international commitments much higher. T3 - KFG Working Paper Series - 26 Y1 - 2019 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-423887 SN - 2509-3770 SN - 2509-3762 IS - 26 ER - TY - RPRT A1 - de Wet, Erika T1 - Entrenching international values through positive law BT - The (limited) effect of peremptory norms T2 - KFG Working Paper Series N2 - Underpinning a legal system with certain values and helping to resolve norm conflicts is in domestic legal systems usually achieved through hierarchical superiority of certain norms of a constitutional nature. The present paper examines the question whether jus cogens can discharge this function within the traditionally horizontal and decentralized international legal order. In so doing, it commences with an overview of the historical origins of peremptory norms in legal scholarship, followed by its endorsement by positive law and courts and tribunals. This analysis illustrates that there are lingering uncertainties pertaining to the process of identification of peremptory norms. Even so, the concept has been invoked in State executive practice (although infrequently) and has been endorsed by various courts. However, such invocation thus far has had a limited impact from a legal perspective. It was mainly confined to a strengthened moral appeal and did in particular not facilitate the resolution of norm conflicts. The contribution further suggests that this limited impact results from the fact that the content of peremptory obligations is either very narrow or very vague. This, in turn, implies a lack of consensus amongst States regarding the content (scope) of jus cogens, including the values underlying these norms. As a result, it is questionable whether the construct of jus cogens is able to provide meaningful legal protection against the erosion of legal norms. It is too rudimentary in character to entrench and stabilize core human rights values as the moral foundation of the international legal order. T3 - KFG Working Paper Series - 25 Y1 - 2019 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-423859 SN - 2509-3770 SN - 2509-3762 IS - 25 ER - TY - THES A1 - Al Nakeeb, Noah T1 - Self-assembly and crosslinking approaches of double hydrophilic linear-brush block copolymers BT - a biocompatible platform for the next generation of nanoreactors Y1 - 2019 ER - TY - THES A1 - Küçükgöze, Gökhan T1 - Purification and characterization of mouse aldehyde oxidases T1 - Aufreinigung und Charakterisierung von Maus-Aldehyd-Oxidasen N2 - Mouse aldehyde oxidases (mAOXs) have a homodimeric structure and belong to xanthine oxidase family of molybdo-flavoenzymes. In general, each dimer is characterized by three subdomains: a 20 kDa N-terminal 2x[2Fe2S] cluster containing domain, a 40 kDa central FAD-containing domain and an 85 kDa C-terminal molybdenum cofactor (Moco) containing domain. Aldehyde oxidases have a broad substrate specificity including the oxidation of different aldehydes and N-heterocyclic compounds. AOX enzymes are present in mainly all eukaryotes. Four different homologs of AOX were identified to be present with varying numbers among species and rodents like mice and rats contain the highest number of AOX isoenzymes. There are four identified homologs in mouse named mAOX1, mAOX3, mAOX2, and mAOX4. The AOX homologs in mice are expressed in a tissue-specific manner. Expression of mAOX1 and mAOX3 are almost superimposable and predominantly synthesized in liver, lung, and testis. The richest source of mAOX4 is the Harderian gland, which is found within the eye's orbit in tetrapods. Expression of mAOX2 is strictly restricted to the Bowman’s gland, the main secretory organ of the nasal mucosa. In this study, the four catalytically active mAOX enzymes were expressed in a heterologous expression system in Escherichia coli and purified in a catalytically active form. Thirty different structurally related aromatic, aliphatic and N-heterocyclic compounds were used as substrates, and the kinetic parameters of all four mAOX enzymes were directly compared. The results showed that all enzymes can catalyze a broad range of substrates. Generally, no major differences between mAOX1, mAOX3 and mAOX2 were identified and the substrate specificity of mAOX1, mAOX3, and mAOX2 was broader compared to that of mAOX4 since mAOX4 showed no activity with substrates like methoxy-benzaldehydes, phenanthridine, N1-methyl-nicotinamide, and cinnamaldehyde and 4-(dimethylamino)cinnamaldehyde. We investigated differences at the flavin site of the mAOX enzymes by measuring the ability of the four mAOX enzymes to oxidize NADH in the absence of oxygen. NADH was able to reduce only mAOX3. The four mouse AOXs are also characterized by quantitative differences in their ability to produce superoxide radicals. mAOX2 is the enzyme generating the largest rate of superoxide radicals of around 40% in relation to moles of substrate converted and it is followed by mAOX1 with a ratio of 30%. To understand the factors that contribute to the substrate specificity of mAOX4, site-directed mutagenesis was applied to substitute amino acids in the substrate-binding funnel by the ones present in mAOX1, mAOX3, and mAOX2. The amino acids Val1016, Ile1018 and Met1088 were selected as targets. An increase in activity was obtained by the amino acid exchange M1088V in the active site identified to be specific for mAOX4, to the amino acid identified in mAOX3. N2 - Mouse aldehyde oxidases (mAOXs) have a homodimeric structure and belong to xanthine oxidase family of molybdo-flavoenzymes. In general, each dimer is characterized by three subdomains: a 20 kDa N-terminal 2x[2Fe2S] cluster containing domain, a 40 kDa central FAD-containing domain and an 85 kDa C-terminal molybdenum cofactor (Moco) containing domain. Aldehyde oxidases have a broad substrate specificity including the oxidation of different aldehydes and N-heterocyclic compounds. AOX enzymes are present in mainly all eukaryotes. Four different homologs of AOX were identified to be present with varying numbers among species and rodents like mice and rats contain the highest number of AOX isoenzymes. There are four identified homologs in mouse named mAOX1, mAOX3, mAOX2, and mAOX4. The AOX homologs in mice are expressed in a tissue-specific manner. Expression of mAOX1 and mAOX3 are almost superimposable and predominantly synthesized in liver, lung, and testis. The richest source of mAOX4 is the Harderian gland, which is found within the eye's orbit in tetrapods. Expression of mAOX2 is strictly restricted to the Bowman’s gland, the main secretory organ of the nasal mucosa. In this study, the four catalytically active mAOX enzymes were expressed in a heterologous expression system in Escherichia coli and purified in a catalytically active form. Thirty different structurally related aromatic, aliphatic and N-heterocyclic compounds were used as substrates, and the kinetic parameters of all four mAOX enzymes were directly compared. The results showed that all enzymes can catalyze a broad range of substrates. Generally, no major differences between mAOX1, mAOX3 and mAOX2 were identified and the substrate specificity of mAOX1, mAOX3, and mAOX2 was broader compared to that of mAOX4 since mAOX4 showed no activity with substrates like methoxy-benzaldehydes, phenanthridine, N1-methyl-nicotinamide, and cinnamaldehyde and 4-(dimethylamino)cinnamaldehyde. We investigated differences at the flavin site of the mAOX enzymes by measuring the ability of the four mAOX enzymes to oxidize NADH in the absence of oxygen. NADH was able to reduce only mAOX3. The four mouse AOXs are also characterized by quantitative differences in their ability to produce superoxide radicals. mAOX2 is the enzyme generating the largest rate of superoxide radicals of around 40% in relation to moles of substrate converted and it is followed by mAOX1 with a ratio of 30%. To understand the factors that contribute to the substrate specificity of mAOX4, site-directed mutagenesis was applied to substitute amino acids in the substrate-binding funnel by the ones present in mAOX1, mAOX3, and mAOX2. The amino acids Val1016, Ile1018 and Met1088 were selected as targets. An increase in activity was obtained by the amino acid exchange M1088V in the active site identified to be specific for mAOX4, to the amino acid identified in mAOX3. KW - aldehyde oxidase KW - drug metabolism KW - molybdenum cofactor KW - enzyme isoforms KW - enzyme kinetics KW - Aldehyd-oxidase KW - Metabolismus von Medikamenten KW - Molybdänkofaktor KW - Isoenzyme KW - Enzymkinetik Y1 - 2019 ER - TY - THES A1 - Victor, Vincent T1 - The Role of Bargaining Power T1 - Die Rolle der Verhandlungsmacht BT - How Unions Affect Income Distribution BT - Der Einfluss der Gewerkschaften auf die Einkommensverteilung T2 - Potsdam Economic Papers N2 - Neoclassical theory omits the role of bargaining power in the determination of wages. As a result, the importance of changes in the bargaining position for the development of income shares in the last decades is underestimated. This paper presents a theoretical argument why collective bargaining power is a main determinant of workers’ share of income and how its decline contributed to the severe changes in the distribution of income since the 1980s. In order to confirm this hypothesis, a panel data regression analysis is performed that suggests that unions significantly influence the distribution of income in developed countries. N2 - Die Verhandlungsmacht der beteiligten Akteure bei der Lohnfindung spielt in der neoklassischen Theorie nur eine untergeordnete Rolle. Dementsprechend wird auch ihre Bedeutung für die Entwicklung der Einkommensverteilung unterschätzt. Diese Arbeit präsentiert eine theoretische Argumentation, warum die kollektive Verhandlungsmacht der Arbeitnehmer einer der wichtigsten Bestimmungsfaktoren der Einkommensverteilung ist und wie der Rückgang eben dieser zu den tiefgreifenden Veränderungen in der Einkommensverteilung seit den 1980ern beigetragen hat. Die Hypothese wird durch eine Panelregression gestützt, die auf einen signifikanten Einfluss von Gewerkschaften und Tarifverhandlungen auf die Einkommensverteilung in Industrieländern in den letzten Jahrzehnten hindeutet. T3 - Potsdam Economic Papers - 6 KW - income distribution KW - bargaining power KW - wages KW - collective bargaining KW - unions KW - macroeconomics KW - Einkommensverteilung KW - Verhandlungsmacht KW - Löhne KW - Tarifverhandlungen KW - Gewerkschaften KW - Makröökonomie Y1 - 2019 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-420689 SN - 978-3-86956-449-4 SN - 2197-8069 SN - 2197-8077 IS - 6 PB - Universitätsverlag Potsdam CY - Potsdam ER - TY - GEN A1 - De Cahsan, Binia A1 - Westbury, Michael V. A1 - Drews, Hauke A1 - Tiedemann, Ralph T1 - The complete mitochondrial genome of a European fire-bellied toad (Bombina bombina) from Germany T2 - Postprints der Universität Potsdam Mathematisch-Naturwissenschaftliche Reihe N2 - The European fire-bellied toad, Bombina bombina, is a small aquatic toad belonging to the family Bombinatoridae. The species is native to the lowlands of Central and Eastern Europe, where population numbers have been in decline in recent past decades. Here, we present the first complete mitochondrial genome of the endangered European fire-bellied toad from Northern Germany recovered using iterative mapping. Phylogenetic analyses including other representatives of the Bombinatoridae placed our German specimen as sister to a Polish B. bombina sequence with high support. This finding is congruent with the postulated Pleistocene history of the species. Our complete mitochondrial genome represents an important resource for further population analysis of the European fire-bellied toad, especially those found within Germany. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 532 KW - Bombina bombina KW - Fire-bellied toad KW - mitogenome KW - conservation genetics KW - population delimitation Y1 - 2019 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-423222 SN - 1866-8372 IS - 532 ER - TY - JOUR A1 - De Cahsan, Binia A1 - Westbury, Michael V. A1 - Drews, Hauke A1 - Tiedemann, Ralph T1 - The complete mitochondrial genome of a European fire-bellied toad (Bombina bombina) from Germany JF - Mitochondrial DNA Part B N2 - The European fire-bellied toad, Bombina bombina, is a small aquatic toad belonging to the family Bombinatoridae. The species is native to the lowlands of Central and Eastern Europe, where population numbers have been in decline in recent past decades. Here, we present the first complete mitochondrial genome of the endangered European fire-bellied toad from Northern Germany recovered using iterative mapping. Phylogenetic analyses including other representatives of the Bombinatoridae placed our German specimen as sister to a Polish B. bombina sequence with high support. This finding is congruent with the postulated Pleistocene history of the species. Our complete mitochondrial genome represents an important resource for further population analysis of the European fire-bellied toad, especially those found within Germany. KW - Bombina bombina KW - Fire-bellied toad KW - mitogenome KW - conservation genetics KW - population delimitation Y1 - 2019 U6 - https://doi.org/10.1080/23802359.2018.1547143 SN - 2380-2359 VL - 4 IS - 1 SP - 498 EP - 500 PB - Taylor & Francis Group CY - London ER -