TY - JOUR A1 - Vergau, Hans-Joachim T1 - Die Rolle Deutschlands bei der Lösung der Namibia-Frage im Rahmen der Vereinten Nationen JF - Die Vereinten Nationen vor globalen Herausforderungen : Referate der Potsdamer UNO-Konferenzen 2000–2008 Y1 - 2011 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-61050 SP - 181 EP - 191 PB - Universitätsverlag Potsdam CY - Potsdam ER - TY - JOUR A1 - Veith, Mehde T1 - Zwischen Vereinheitlichung und Vielfalt BT - Die Verwaltungsentwicklung im vereinten Deutschland JF - Potsdamer Studien zu Staat, Recht und Politik N2 - Inhalt: - I. Einleitung - II. Entwicklungsbedingungen und Probleme - II.1. Die konkrete Problemlage nach 1989 - II.2. Überlagernde Effekte - III. Die Lösungsansätze - III.1. Funktional- und Gebietsreform - III.2. Qualitätsaspekte - III.3. Reaktion auf Europäisierung - III.4. Adaption von Tendenzen aus der Privatwirtschaft - IV. Fazit Y1 - 2011 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-60719 SN - 1867-2663 SN - 1869-2443 IS - 3 SP - 33 EP - 52 PB - Universitätsverlag Potsdam CY - Potsdam ER - TY - JOUR A1 - Vater, Marianne A1 - Koessl, Manfred T1 - Comparative aspects of cochlear functional organization in mammals JF - Hearing research N2 - This review addresses the functional organization of the mammalian cochlea under a comparative and evolutionary perspective. A comparison of the monotreme cochlea with that of marsupial and placental mammals highlights important evolutionary steps towards a hearing organ dedicated to process higher frequencies and a larger frequency range than found in non-mammalian vertebrates. Among placental mammals, there are numerous cochlear specializations which relate to hearing range in adaptation to specific habitats that are superimposed on a common basic design. These are illustrated by examples of specialist ears which evolved excellent high frequency hearing and echolocation (bats and dolphins) and by the example of subterranean rodents with ears devoted to processing low frequencies. Furthermore, structural functional correlations important for tonotopic cochlear organization and predictions of hearing capabilities are discussed. Y1 - 2011 U6 - https://doi.org/10.1016/j.heares.2010.05.018 SN - 0378-5955 VL - 273 IS - 1-2 SP - 89 EP - 99 PB - Elsevier CY - Amsterdam ER - TY - BOOK A1 - Vasishth, Shravan A1 - Broe, Michael T1 - The foundations of statistics: a simulation-based approach Y1 - 2011 SN - 978-3-642-16312-8 U6 - https://doi.org/10.1007/978-3-642-16313-5 PB - Springer-Verlag Berlin Heidelberg CY - Berlin, Heidelberg ER - TY - JOUR A1 - Vargas, Gabriel A1 - Farias, Marcelo A1 - Carretier, Sebastien A1 - Tassara, Andres A1 - Baize, Stephane A1 - Melnick, Daniel T1 - Coastal uplift and tsunami effects associated to the 2010 M(w)8.8 Maule earthquake in Central Chile JF - Andean geology N2 - On February 27, 2010 at 03:34:08 AM an M(w)8.8 earthquake, with epicenter located off Cobquecura (73.24 degrees W; 36.29 degrees S), severely hit Central Chile. The tsunami waves that followed this event affected the coastal regions between the cities of Valparaiso and Valdivia, with minor effects as far as Coquimbo. The earthquake occurred along the subduction of the Nazca oceanic plate beneath the South American plate. Coseismic coastal uplift was estimated through observations of bleached lithothamnioids crustose coralline algae, which were exposed after the mainshock between 34.13 degrees S and 38.34 degrees S, suggesting the latitudinal distribution of the earthquake rupture. The measured coastal uplift values varied between 240 +/- 20 cm at sites closer to the trench along the western coast of the Arauco peninsula and 15 +/- 10 cm at sites located farther east. A maximum value of 260 +/- 50 cm was observed at the western coast of Santa Maria Island, which is similar to the reported uplift associated with the 1835 earthquake at Concepcion. Land subsidence values on the order of 0.5 m to 1 m evidenced a change in polarity and position of the coseismic hinge at 110-120 km from the trench. In four sites along the coast we observed a close match between coastal uplift values deduced from bleached lithothamnioids algae and GPS measurements. According to field observations tsunami heights reached ea. 14 m in the coastal area of the Maule Region immediately north of the epicenter, and diminished progressively northwards to 4-2 m near Valparaiso. Along the coast of Cobquecura, tsunami height values were inferior to 2-4 m. More variable tsunami heights of 6-8 m were measured at Dichato-Talcahuano and Tirua-Puerto Saavedra, in the Biobio and Arauco regions, respectively, to the south of the epicenter. According to eyewitnesses, the tsunami reached the coast between 12 to 20 and 30 to 45 minutes in areas located closer and faraway from the earthquake rupture zone, respectively. Destructive tsunami waves arrived also between 2.5 and 4.5 hours after the mainshock, especially along the coast of the Biobio and Arauco regions. The tsunami effects were highly variable along the coast, as a result of geomorphological and bathymetric local conditions, besides potential complexities induced by the main shock. KW - M(w)8.8 Maule earthquake KW - Central Chile KW - Coseismic coastal uplift KW - Tsunami effect Y1 - 2011 U6 - https://doi.org/10.5027/andgeoV38n1-a12 SN - 0718-7106 VL - 38 IS - 1 SP - 219 EP - 238 PB - Servicio Nacional de Geologìa y Minerìa CY - Santiago ER - TY - GEN A1 - Van Donk, Ellen A1 - Ianora, Adrianna A1 - Vos, Matthijs T1 - Induced defences in marine and freshwater phytoplankton BT - a review T2 - Postprints der Universität Potsdam : Mathematisch Naturwissenschaftliche Reihe N2 - Many organisms have developed defences to avoid predation by species at higher trophic levels. The capability of primary producers to defend themselves against herbivores affects their own survival, can modulate the strength of trophic cascades and changes rates of competitive exclusion in aquatic communities. Algal species are highly flexible in their morphology, growth form, biochemical composition and production of toxic and deterrent compounds. Several of these variable traits in phytoplankton have been interpreted as defence mechanisms against grazing. Zooplankton feed with differing success on various phytoplankton species, depending primarily on size, shape, cell wall structure and the production of toxins and deterrents. Chemical cues associated with (i) mechanical damage, (ii) herbivore presence and (iii) grazing are the main factors triggering induced defences in both marine and freshwater phytoplankton, but most studies have failed to disentangle the exact mechanism(s) governing defence induction in any particular species. Induced defences in phytoplankton include changes in morphology (e.g. the formation of spines, colonies and thicker cell walls), biochemistry (such as production of toxins, repellents) and in life history characteristics (formation of cysts, reduced recruitment rate). Our categorization of inducible defences in terms of the responsible induction mechanism provides guidance for future work, as hardly any of the available studies on marine or freshwater plankton have performed all the treatments that are required to pinpoint the actual cue(s) for induction. We discuss the ecology of inducible defences in marine and freshwater phytoplankton with a special focus on the mechanisms of induction, the types of defences, their costs and benefits, and their consequences at the community level. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 881 KW - defenses KW - algae KW - review KW - plankton community KW - cyanobacteria KW - toxins Y1 - 2020 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-435130 SN - 1866-8372 IS - 881 ER - TY - JOUR A1 - Van Donk, Ellen A1 - Ianora, Adrianna A1 - Vos, Matthijs T1 - Induced defences in marine and freshwater phytoplankton a review JF - Hydrobiologia : acta hydrobiologica, hydrographica, limnologica et protistologica N2 - Many organisms have developed defences to avoid predation by species at higher trophic levels. The capability of primary producers to defend themselves against herbivores affects their own survival, can modulate the strength of trophic cascades and changes rates of competitive exclusion in aquatic communities. Algal species are highly flexible in their morphology, growth form, biochemical composition and production of toxic and deterrent compounds. Several of these variable traits in phytoplankton have been interpreted as defence mechanisms against grazing. Zooplankton feed with differing success on various phytoplankton species, depending primarily on size, shape, cell wall structure and the production of toxins and deterrents. Chemical cues associated with (i) mechanical damage, (ii) herbivore presence and (iii) grazing are the main factors triggering induced defences in both marine and freshwater phytoplankton, but most studies have failed to disentangle the exact mechanism(s) governing defence induction in any particular species. Induced defences in phytoplankton include changes in morphology (e.g. the formation of spines, colonies and thicker cell walls), biochemistry (such as production of toxins, repellents) and in life history characteristics (formation of cysts, reduced recruitment rate). Our categorization of inducible defences in terms of the responsible induction mechanism provides guidance for future work, as hardly any of the available studies on marine or freshwater plankton have performed all the treatments that are required to pinpoint the actual cue(s) for induction. We discuss the ecology of inducible defences in marine and freshwater phytoplankton with a special focus on the mechanisms of induction, the types of defences, their costs and benefits, and their consequences at the community level. KW - Defenses KW - Algae KW - Review KW - Plankton community KW - Cyanobacteria KW - Toxins Y1 - 2011 U6 - https://doi.org/10.1007/s10750-010-0395-4 SN - 0018-8158 SN - 1573-5117 VL - 668 IS - 1 SP - 3 EP - 19 PB - Springer CY - Dordrecht ER - TY - JOUR A1 - van Afferden, Manfred A1 - Rahman, Khaja Z. A1 - Mosig, Peter A1 - De Biase, Cecilia A1 - Thullner, Martin A1 - Oswald, Sascha A1 - Müller, Roland A. T1 - Remediation of groundwater contaminated with MTBE and benzene the potential of vertical-flow soil filter systems JF - Water research N2 - Field investigations on the treatment of MTBE and benzene from contaminated groundwater in pilot or full-scale constructed wetlands are lacking hugely. The aim of this study was to develop a biological treatment technology that can be operated in an economic, reliable and robust mode over a long period of time. Two pilot-scale vertical-flow soil filter eco-technologies, a roughing filter (RF) and a polishing filter (PF) with plants (willows), were operated independently in a single-stage configuration and coupled together in a multi-stage (RF + PF) configuration to investigate the MTBE and benzene removal performances. Both filters were loaded with groundwater from a refinery site contaminated with MTBE and benzene as the main contaminants, with a mean concentration of 2970 +/- 816 and 13,966 +/- 1998 mu g L(-1), respectively. Four different hydraulic loading rates (HLRs) with a stepwise increment of 60, 120, 240 and 480 L m(-2) d(-1) were applied over a period of 388 days in the single-stage operation. At the highest HLR of 480 L m(-2)d(-1), the mean concentrations of MTBE and benzene were found to be 550 +/- 133 and 65 +/- 123 mu g L(-1) in the effluent of the RF. In the effluent of the PP system, respective mean MTBE and benzene concentrations of 49 +/- 77 and 0.5 +/- 0.2 mu g L(-1) were obtained, which were well below the relevant MTBE and benzene limit values of 200 and 1 mu g L-1 for drinking water quality. But a dynamic fluctuation in the effluent MTBE concentration showed a lack of stability in regards to the increase in the measured values by nearly 10%, which were higher than the limit value. Therefore, both (RF + PF) filters were combined in a multi-stage configuration and the combined system proved to be more stable and effective with a highly efficient reduction of the MTBE and benzene concentrations in the effluent. Nearly 70% of MTBE and 98% of benzene were eliminated from the influent groundwater by the first vertical filter (RF) and the remaining amount was almost completely diminished (similar to 100% reduction) after passing through the second filter (PF), with a mean MTBE and benzene concentration of 5 +/- 10 and 0.6 +/- 0.2 mu g L(-1) in the final effluent. The emission rate of volatile organic compounds mass into the air from the systems was less than 1% of the inflow mass loading rate. The results obtained in this study not only demonstrate the feasibility of vertical-flow soil filter systems for treating groundwater contaminated with MTBE and benzene, but can also be considered a major step forward towards their application under full-scale conditions for commercial purposes in the oil and gas industries. KW - Benzene KW - Groundwater remediation KW - Hydraulic loading rate KW - MTBE KW - Pilot-scale constructed wetland KW - Vertical-flow soil filter KW - Willow tree Y1 - 2011 U6 - https://doi.org/10.1016/j.watres.2011.07.010 SN - 0043-1354 VL - 45 IS - 16 SP - 5063 EP - 5074 PB - Elsevier CY - Oxford ER - TY - THES A1 - Valverde Serrano, Clara T1 - Self-assembly behavior in hydrophilic block copolymers T1 - Selbstorganisation von hydrophilen Blockcopolymeren N2 - Block copolymers are receiving increasing attention in the literature. Reports on amphiphilic block copolymers have now established the basis of their self-assembly behavior: aggregate sizes, morphologies and stability can be explained from the absolute and relative block lengths, the nature of the blocks, the architecture and also solvent selectiveness. In water, self-assembly of amphiphilic block copolymers is assumed to be driven by the hydrophobic. The motivation of this thesis is to study the influence on the self-assembly in water of A b B type block copolymers (with A hydrophilic) of the variation of the hydrophilicity of B from non-soluble (hydrophobic) to totally soluble (hydrophilic). Glucose-modified polybutadiene-block-poly(N-isopropylacrylamide) copolymers were prepared and their self-assembly behavior in water studied. The copolymers formed vesicles with an asymmetric membrane with a glycosylated exterior and poly(N-isopropylacrylamide) on the inside. Above the low critical solution temperature (LCST) of poly(N-isopropylacrylamide), the structure collapsed into micelles with a hydrophobic PNIPAM core and glycosylated exterior. This collapse was found to be reversible. As a result, the structures showed a temperature-dependent interaction with L-lectin proteins and were shown to be able to encapsulate organic molecules. Several families of double hydrophilic block copolymers (DHBC) were prepared. The blocks of these copolymers were biopolymers or polymer chimeras used in aqueous two-phase partition systems. Copolymers based on dextran and poly(ethylene glycol) blocks were able to form aggregates in water. Dex6500-b-PEG5500 copolymer spontaneously formed vesicles with PEG as the “less hydrophilic” barrier and dextran as the solubilizing block. The aggregates were found to be insensitive to the polymer's architecture and concentration (in the dilute range) and only mildly sensitive to temperature. Variation of the block length, yielded different morphologies. A longer PEG chain seemed to promote more curved aggregates following the inverse trend usually observed in amphiphilic block copolymers. A shorter dextran promoted vesicular structures as usually observed for the amphiphilic counterparts. The linking function was shown to have an influence of the morphology but not on the self-assembly capability in itself. The vesicles formed by dex6500-b-PEG5500 showed slow kinetics of clustering in the presence of Con A lectin. In addition both dex6500-b-PEG5500 and its crosslinked derivative were able to encapsulate fluorescent dyes. Two additional dextran-based copolymers were synthesized, dextran-b-poly(vinyl alcohol) and dextran-b-poly(vinyl pyrrolidone). The study of their self-assembly allowed to conclude that aqueous two-phase systems (ATPS) is a valid source of inspiration to conceive DHBCs capable of self-assembling. In the second part the principle was extended to polypeptide systems with the synthesis of a poly(N-hydroxyethylglutamine)-block-poly(ethylene glycol) copolymer. The copolymer that had been previously reported to have emulsifying properties was able to form vesicles by direct dissolution of the solid in water. Last, a series of thermoresponsive copolymers were prepared, dextran-b-PNIPAMm. These polymers formed aggregates below the LCST. Their structure could not be unambiguously elucidated but seemed to correspond to vesicles. Above the LCST, the collapse of the PNIPAM chains induced the formation of stable objects of several hundreds of nanometers in radius that evolved with increasing temperature. The cooling of these solution below LCST restored the initial aggregates. This self-assembly of DHBC outside any stimuli of pH, ionic strength, or temperature has only rarely been described in the literature. This work constituted the first formal attempt to frame the phenomenon. Two reasons were accounted for the self-assembly of such systems: incompatibility of the polymer pairs forming the two blocks (enthalpic) and a considerable solubility difference (enthalpic and entropic). The entropic contribution to the positive Gibbs free energy of mixing is believed to arise from the same loss of conformational entropy that is responsible for “the hydrophobic effect” but driven by a competition for water of the two blocks. In that sense this phenomenon should be described as the “hydrophilic effect”. N2 - Blockcopolymere erfahren ein stetig wachsendes Interesse, was an der steigenden Anzahl an Publikationen zu diesem Thema erkennbar ist. Zahlreiche Studien zu amphiphilen Blockcopolymeren haben dabei einige grundlegende Erkenntnisse über deren chemisches und physikalisches Verhalten, vor allem über die Selbstorganisation, hervorgebracht. So können die Größe, die verschiedenen Morphologien und auch die Stabilität der gebildeten Aggregate anhand der relativen und absoluten Blocklängen, die chemischen Struktur der Blöcke, der molekularen Architektur und der Eigenschaften des verwendeten Lösungsmittel erklärt werden. Im speziellen Fall des Wassers als Lösungsmittel bist die Selbstorganisation amphiphiler Blockcopolymere durch den hydrophoben Effekt bedingt. Dieser Arbeit liegt das Interesse an der Selbstorganisation in wässrigem Medium von Blockcopolymeren des Typs A-b-B mit A als hydrophilem Block und B als Block mit variierender Hydrophilie bzw. Hydrophpobie von unlöslich bis vollständig löslich zugrunde. Durch Variation dieser Eigenschaften von Block B soll dessen Einfluss auf das Selbstorganisationsverhalten untersucht werden. Dazu wurden mit Glucose modifizierte Polybutadien-block-Poly(N-Isopropylacrylamid)-Copolymere hergestellt und deren Selbstorganisation in Wasser untersucht. Die Copolymere bilden Vesikel mit einer asymmetrischen Membran, wobei im äußeren Bereich glycolysierte Gruppen und im inneren Bereich Poly(N-Isopropylacrylamid) (PNIPAM) vorliegen. Beim Überschreiten der low critical solution temperature (LCST) kollabiert die vesikuläre Struktur unter Bildung von Mizellen mit einem hydrophoben PNIPAM-Mizellinneren und nach außen gerichteten glycolysierten Blöcken. Diese strukturelle Umwandlung ist reversibel. Die Strukturen zeigten außerdem eine temperaturabhängige Wechselwirkung mit L-Lectin-Proteinen und die Möglichkeit zur Einkapselung organischer Moleküle konnte belegt werden. Des weiteren wurden verschiedene Gruppen von Blockcopolymeren mit zwei hydrophilen Blöcken synthetisiert (double hydrophilic block copolymers – DHBC). Die Blöcke dieser Systeme waren entweder Biopolymere oder Polymerchimäre, die in wässrigen Zwei-Phasen-Trennverfahren eingesetzt werden. Polymere, die auf Dextran- und Poly(ethylenglycol)-Blöcken basieren, zeigen Aggregatbildung in wässriger Phase. Dex6500-b-PEG5500 bildet spontan Vesikel mit PEG als „weniger hydrophilem“ Bestandteil und Dextran als löslichem Block. Die Bildung dieser Vesikel zeigte keine Emfpindlichkeit gegenüber einer Veränderung der Polymerarchitektur und der Konzentration, und nur eine geringe Sensitivität gegenüber Temperaturänderungen. Veränderungen der Blocklängen dagegen beeinflussten die Selbstorganisation und führten zu unterschiedlichen Morphologien. Längere PEG-Blöcke bevorzugten dabei die Bildung eher gekrümmter Aggregate, entgegen dem Trend, der gewöhnlicherweise für amphiphile Blockcopolymere beobachtet wird. Die Verkürzung des Dextran-Blocks fördert die Ausbildung vesikulärer Strukturen, was dem Verhalten der amphiphilen Gegenspieler der DHBC-Systeme entspricht. Die funktionelle Gruppe zur Verbindung der beiden Blöcke hat zwar einen Einfluss auf die Morphologie der gebildeten Aggregate, nicht jedoch auf die eigentliche Fähigkeit der Systeme zur Selbstorganisation. Die Dex6500-b-PEG5500-Vesikel wiesen zudem eine langsame Bildungskinetik in Gegenwart von Con-A-Lectin auf. Des Weiteren waren sowohl Dex6500-b-PEG5500 als auch das quervernetzte Derivate dieses Copolymers in der Lage, Fluoreszenzfarbstoffe einzulagern. Um zu zeigen, dass wässrige Zwei-Phasen-Systeme (aqueous two phase systems – ATPS) eine belastbare Grundlage für die Untersuchung und Entwicklung selbstorganisierender DHBC-Systeme sind, wurden weitere Dextran-basierte Copolymere synthetsisiert: Dextran-b-Poly(vinylalokohol) und Detran-b-Poly(vinylpyrrolidon). In einem zweiten Teil dieser Arbeit wurde das zuvor erarbeitete Prinzip auf auf Polypeptidsysteme ausgeweitet. Dazu wurde ein Poly(N-Hydroxyethylglutamin)-block-Poly(ethylenglycol)-Copolymer hergestellt. Dieses Copolymer, dessen emulgierenden Eigenschaften bereits bekannt waren, wies unmittelbar nach Lösung des Feststoffes in Wasser Vesikelbildung auf. In einem dritten Teil der Studie wurden thermoresponsive Copolymere hergestellt und untersucht: Dextran-b-PNIPAMm. Unterhalb der LCST konnte die Bildung von Aggregaten nachgewiesen werden, deren Struktur nicht zweifelsfrei entschlüsselt werden konnte, wobei jedoch zahlreiche Hinweise auf eine vesikuläre Struktur hindeuten. Oberhalb der LCST wurde durch die Kollabierung der PNIPAM-Ketten die Bildung stabiler Strukturen mit Radien von mehreren hundert Nanometern induziert, deren weitere Entwicklung durch eine weitere Temperaturerhöhung gefördert werden konnte. Durch Rückkühlung in den Temperaturebereich unterhalb der LCST konnten die zuvor beobachteten Aggregate reversibel zurückgebildet werden. Das Selbstorganisationsverhalten von DHBC, unabhängig vom Einfluss des pH-Werts, der Ionenstärke oder der Temperatur are bisher nur in sehr geringem Umfang Gegenstand wissenschaftlicher Veröffentlichungen. Diese Arbeit stellt damit den ersten umfassenden Beitrag zur systematischen Erarbeitung dieses Phänomens dar. Es konnten dabei zwei Ursachen für die beobachteten Selbstorganisationseffekte bestimmt werden: die Inkompatibilität der beiden Polymerblöcke (enthalpischer Effekt) und der Unterschied in deren Löslichkeit (enthalpische und entropische Effekte). Der entropische Beitrag zur positiven Gibbs’schen Freien Mischungsenergie wird dem selben Verlust konformativer Entropie zugeordnet, der auch für den hydrophoben Effekt verantwortlich ist, allerdings angetrieben durch einen Wettbewerb der beiden Polymerblöcke um das Wasser. In diesem Sinne kann man das beobachtete Phänomen als „hydrophilen Effekt“ bezeichnen. KW - Selbstorganisation KW - Blockcopolymere KW - hydrophil KW - self-assembly KW - copolymers KW - hydrophilic Y1 - 2011 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-54163 ER - TY - JOUR A1 - Valleriani, Angelo A1 - Zhang, Gong A1 - Nagar, Apoorva A1 - Ignatova, Zoya A1 - Lipowsky, Reinhard T1 - Length-dependent translation of messenger RNA by ribosomes JF - Physical review : E, Statistical, nonlinear and soft matter physics N2 - A simple measure for the efficiency of protein synthesis by ribosomes is provided by the steady state amount of protein per messenger RNA (mRNA), the so-called translational ratio, which is proportional to the translation rate. Taking the degradation of mRNA into account, we show theoretically that both the translation rate and the translational ratio decrease with increasing mRNA length, in agreement with available experimental data for the prokaryote Escherichia coli. We also show that, compared to prokaryotes, mRNA degradation in eukaryotes leads to a less rapid decrease of the translational ratio. This finding is consistent with the fact that, compared to prokaryotes, eukaryotes tend to have longer proteins. Y1 - 2011 U6 - https://doi.org/10.1103/PhysRevE.83.042903 SN - 1539-3755 VL - 83 IS - 4 PB - American Physical Society CY - College Park ER -