TY - JOUR A1 - Khelifi, N. A1 - Sarnthein, M. A1 - Naafs, B. D. A. T1 - Technical note: Late Pliocene age control and composite depths at ODP Site 982, revisited JF - CLIMATE OF THE PAST N2 - Ocean Drilling Program (ODP) Site 982 provided a key sediment section at Rockall Plateau for reconstructing northeast Atlantic paleoceanography and monitoring benthic delta O-18 stratigraphy over the late Pliocene to Quaternary onset of major Northern Hemisphere glaciation. A renewed hole-specific inspection of magnetostratigraphic reversals and the addition of epibenthic delta O-18 records for short Pliocene sections in holes 982A, B, and C, crossing core breaks in the delta O-18 record published for Hole 982B, now imply a major revision of composite core depths. After tuning to the orbitally tuned reference record LR04, the new composite delta O-18 record results in a hiatus, where the Kaena magnetic subchron might have been lost, and in a significant age reduction for all proxy records by 130 to 20 ky over the time span 3.2-2.7 million years ago (Ma). Our study demonstrates the general significance of reliable composite-depth scales and delta O-18 stratigraphies in ODP sediment records for generating ocean-wide correlations in paleoceanography. The new concept of age control makes the late Pliocene trends in SST (sea surface temperature) and atmospheric pCO(2) at Site 982 more consistent with various paleoclimate trends published from elsewhere in the North Atlantic. Y1 - 2012 U6 - https://doi.org/10.5194/cp-8-79-2012 SN - 1814-9324 VL - 8 IS - 1 SP - 79 EP - 87 PB - COPERNICUS GESELLSCHAFT MBH CY - GOTTINGEN ER - TY - JOUR A1 - Knoops, Femke A1 - Erbil, Fethiye A1 - Ertürk, Mustafa T1 - Teaching patterns and trends JF - Potsdamer geographische Praxis N2 - 1. Outline 2. Definition 3. Why is it important (or not) to teach about patterns and trends? What are the strengths and weaknesses of teaching patterns and trends? 4. How were patterns and trends offered in the original assignments? 5. What did the student teacher change in practice? How did it go? 6. Suggestions for improving patterns and trends KW - Europäische Werteerziehung KW - Familie KW - Lehrevaluation KW - Studierendenaustausch KW - Unterrichtseinheiten KW - Curriculum Framework KW - European values education KW - Family KW - lesson evaluation KW - student exchange KW - teaching units KW - curriculum framework Y1 - 2012 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-65845 SN - 2194-1599 SN - 2194-1602 IS - 1 SP - 75 EP - 79 PB - Universitätsverlag Potsdam CY - Potsdam ER - TY - BOOK A1 - Uhlenwinkel, Anke A1 - Krause, Uwe A1 - Halman, Loek A1 - Rokven, Josja A1 - Sieben, Inge A1 - Pažický, Michal A1 - Blahušiaková, Andrea A1 - Röper-Kühnemann, Christian A1 - Staufenbiel, Christoph A1 - Vozárová, Hana A1 - Hintze, Katarina A1 - Ivaška, Michal A1 - Kallenbach, René A1 - Majer, Zdenko A1 - Röll, Juliane A1 - Pisarčík, Stanislav A1 - Weiser, Ines A1 - Seeger, Anett A1 - Strehmann, Anja A1 - Chovanová, Katarina A1 - Gembický, Kamil A1 - Nern, Luise A1 - Cornelissen, Sebastiaan A1 - Turgut, Pelin A1 - Knoops, Femke A1 - Erbil, Fethiye A1 - Ertürk, Mustafa A1 - Akpinar, Seda A1 - Maas, Desiree A1 - Rooth, Anneke A1 - Azar, Elif Zeynep A1 - Erdönmez, Çağlayan A1 - Verscheijden, Desirée A1 - Altuntas, Kezban A1 - Akçay, Pinar A1 - Kools, Suzanne A1 - Schnabel, Richard A1 - van den Beemt, Martijn A1 - Çinkaya, Muhammed A1 - Erdem, Didem Tuğçe A1 - Janssen, Robert ED - Uhlenwinkel, Anke T1 - Teaching about the religious values of Europeans : critical reflections from the second student exchange of the EVE-project N2 - The European Values Education (EVE) project is a large-scale, cross-national, and longitudinal survey research programme on basic human values. The main topic of its second stage was religion in Europe. Student teachers of several universities in Europe worked together in multicultural exchange groups. Their results are presented in this issue. T3 - Potsdamer Geographische Praxis - 1 KW - Europäische Werteerziehung KW - Religion KW - Lehrevaluation KW - Studierendenaustausch KW - Unterrichtseinheiten KW - Curriculum Framework KW - European values education KW - religion KW - lesson evaluation KW - student exchange KW - teaching units KW - curriculum framework Y1 - 2012 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-59010 SN - 978-3-86956-175-2 ER - TY - JOUR A1 - Wildish, J. A1 - Pavesi, Laura A1 - Ketmaier, Valerio T1 - Talitrid amphipods (Crustacea: Amphipoda: Talitridae) and the driftwood ecological niche a morphological and molecular study JF - Journal of natural history : an international journal of systematics, interactive biology and biodiversity. - London : Taylor & Francis   1.1967 - N2 - Coastal regions of the North East Atlantic and Mediterranean Seas have four known species of driftwood talitrids. Records are extremely scanty, often limited to the type locality and dating to 1950. We were able to study three of them, all belonging to the genus Macarorchestia, using fresh and archived samples including type material. Allometric and molecular analyses support: (1) a close relationship among all the three classically defined Macarorchestia species, (2) Macarorchestia was well separated from non-driftwood taxa, and (3) a putative new driftwood talitrid discovered during this study was not closely related to Macarorchestia. Genetic divergence between the new species and Macarorchestia remyi is as high as the average distance among a number of talitrid species included in the study for comparison. A key is provided to identify all three of the presently known species of Macarorchestia, using morphological characters employed in the allometric study. KW - Macarorchestia remyi KW - Macarorchestia roffensis KW - Macarorchestia martini KW - Driftwood habitat KW - COI-DNA barcoding KW - allometry Y1 - 2012 U6 - https://doi.org/10.1080/00222933.2012.717971 SN - 0022-2933 VL - 46 IS - 43-44 SP - 2677 EP - 2700 PB - Routledge, Taylor & Francis Group CY - Abingdon ER - TY - JOUR A1 - Herzog, Marc A1 - Schick, Daniel A1 - Leitenberger, Wolfram A1 - Shayduk, Roman A1 - van der Veen, Renske M. A1 - Milne, Christopher J. A1 - Johnson, Steven Lee A1 - Vrejoiu, Ionela A1 - Bargheer, Matias T1 - Tailoring interference and nonlinear manipulation of femtosecond x-rays JF - New journal of physics : the open-access journal for physics N2 - We present ultrafast x-ray diffraction (UXRD) experiments on different photoexcited oxide superlattices. All data are successfully simulated by dynamical x-ray diffraction calculations based on a microscopic model, that accounts for the linear response of phonons to the excitation laser pulse. Some Bragg reflections display a highly nonlinear strain dependence. The origin of linear and two distinct nonlinear response phenomena is discussed in a conceptually simpler model using the interference of envelope functions that describe the diffraction efficiency of the average constituent nanolayers. The combination of both models facilitates rapid and accurate simulations of UXRD experiments. Y1 - 2012 U6 - https://doi.org/10.1088/1367-2630/14/1/013004 SN - 1367-2630 VL - 14 IS - 1 PB - IOP Publ. Ltd. CY - Bristol ER - TY - JOUR A1 - Andres, Dorothee A1 - Roske, Yvette A1 - Doering, Carolin A1 - Heinemann, Udo A1 - Seckler, Robert A1 - Barbirz, Stefanie T1 - Tail morphology controls DNA release in two Salmonella phages with one lipopolysaccharide receptor recognition system JF - Molecular microbiology N2 - Bacteriophages use specific tail proteins to recognize host cells. It is still not understood to molecular detail how the signal is transmitted over the tail to initiate infection. We have analysed in vitro DNA ejection in long-tailed siphovirus 9NA and short-tailed podovirus P22 upon incubation with Salmonella typhimurium lipopolysaccharide (LPS). We showed for the first time that LPS alone was sufficient to elicit DNA release from a siphovirus in vitro. Crystal structure analysis revealed that both phages use similar tailspike proteins for LPS recognition. Tailspike proteins hydrolyse LPS O antigen to position the phage on the cell surface. Thus we were able to compare in vitro DNA ejection processes from two phages with different morphologies with the same receptor under identical experimental conditions. Siphovirus 9NA ejected its DNA about 30 times faster than podovirus P22. DNA ejection is under control of the conformational opening of the particle and has a similar activation barrier in 9NA and P22. Our data suggest that tail morphology influences the efficiencies of particle opening given an identical initial receptor interaction event. Y1 - 2012 U6 - https://doi.org/10.1111/j.1365-2958.2012.08006.x SN - 0950-382X VL - 83 IS - 6 SP - 1244 EP - 1253 PB - Wiley-Blackwell CY - Hoboken ER - TY - JOUR A1 - Neuvonen, Kari A1 - Neuvonen, Helmi A1 - Koch, Andreas A1 - Kleinpeter, Erich T1 - Taft equation in the light of NBO computations introduction of a novel polar computational substituent constant scale sigma(q)* for alkyl groups JF - Computational and theoretical chemistry N2 - The validity of the Taft equation: log(k(R)/k(CH3)) = rho*sigma* + delta E-S was studied with the aid of NBO computational results concerning cyclohexyl esters RCOOC6H11 [R = Methyl, Ethyl, n-Propyl, Isopropyl, n-Butyl, Isobutyl, sec-Butyl, tert-Butyl, Neopentyl, CH(CH2CH3)(2), CH(CH3)C(CH3)(3), C(CH3)(2)CH2CH3, C(CH3)(2)C(CH3)(3), CH(CH3)(Np), CH(iPr)(tBu), C(Me)(Et)(iPr), C(Et)(2)(tBu) or C(Et)(iPr)(tBu)]. It was proved that the sigma*(alkyl) value is a composite substitutent constant including the polar and steric contributions. A novel computational sigma(q)* substituent constant scale is presented based on the NBO atomic charges of the alpha-carbon and the computational total steric exchange energies E(ster) of the cyclohexyl esters specified above. The method used offers a useful way to calculate sigma*(alkyl) values for alkyl groups for which experimental Taft's polar sigma* parameters are not available. KW - NBO analysis KW - Taft equation KW - Polar substituent constant KW - Steric effect Y1 - 2012 U6 - https://doi.org/10.1016/j.comptc.2011.11.044 SN - 2210-271X VL - 981 IS - 2 SP - 52 EP - 58 PB - Elsevier CY - Amsterdam ER - TY - JOUR A1 - Kleinpeter, Erich A1 - Neuvonen, Kari A1 - Neuvonen, Helmi A1 - Koch, Andreas T1 - Taft equation in the light of NBO computations : Introduction of a novel polar computational substituent constant scale for alkyl groups Y1 - 2012 SN - 2210-271X ER - TY - THES A1 - Irgang, Susann T1 - Systemic characterization of the TOR-signaling pathway in chlamydomonas reinhardtii Y1 - 2012 CY - Potsdam ER - TY - JOUR A1 - Heinz, S. A1 - Jung, I. A1 - Stegmann, Christian T1 - Systematic studies of the Richardson-Lucy deconvolution algorithm applied to VHE gamma data JF - ASTROPARTICLE PHYSICS N2 - The Richardson-Lucy deconvolution algorithm was applied to astronomical images in the very high-energy regime with photon energies above 100 GeV. Through a systematic study with respect to source significance, background level and source morphology we were able to derive optimal deconvolution parameters. The results presented show that deconvolution makes it possible to study structural details well below the angular resolution of the very high-energy gamma-ray experiment. (C) 2012 Elsevier B.V. All rights reserved. KW - Very high energy gamma-ray astronomy KW - Deconvolution Y1 - 2012 U6 - https://doi.org/10.1016/j.astropartphys.2012.05.013 SN - 0927-6505 VL - 36 IS - 1 SP - 146 EP - 150 PB - ELSEVIER SCIENCE BV CY - AMSTERDAM ER - TY - JOUR A1 - Girbig, Dorothee A1 - Grimbs, Sergio A1 - Selbig, Joachim T1 - Systematic analysis of stability patterns in plant primary metabolism JF - PLoS one N2 - Metabolic networks are characterized by complex interactions and regulatory mechanisms between many individual components. These interactions determine whether a steady state is stable to perturbations. Structural kinetic modeling (SKM) is a framework to analyze the stability of metabolic steady states that allows the study of the system Jacobian without requiring detailed knowledge about individual rate equations. Stability criteria can be derived by generating a large number of structural kinetic models (SK-models) with randomly sampled parameter sets and evaluating the resulting Jacobian matrices. Until now, SKM experiments applied univariate tests to detect the network components with the largest influence on stability. In this work, we present an extended SKM approach relying on supervised machine learning to detect patterns of enzyme-metabolite interactions that act together in an orchestrated manner to ensure stability. We demonstrate its application on a detailed SK-model of the Calvin-Benson cycle and connected pathways. The identified stability patterns are highly complex reflecting that changes in dynamic properties depend on concerted interactions between several network components. In total, we find more patterns that reliably ensure stability than patterns ensuring instability. This shows that the design of this system is strongly targeted towards maintaining stability. We also investigate the effect of allosteric regulators revealing that the tendency to stability is significantly increased by including experimentally determined regulatory mechanisms that have not yet been integrated into existing kinetic models. Y1 - 2012 U6 - https://doi.org/10.1371/journal.pone.0034686 SN - 1932-6203 VL - 7 IS - 4 PB - PLoS CY - San Fransisco ER - TY - JOUR A1 - Kleinpeter, Erich A1 - Lazareva, Nataliya F. A1 - Shainyan, Bagrat A. A1 - Schilde, Uwe A1 - Chipania, Nina N. T1 - Synthesis, Molecular Structure, Conformational Analysis, and Chemical Properties of Silicon-Containing Derivatives of Quinolizidine Y1 - 2012 SN - 0022-3263 ER - TY - JOUR A1 - Lazareva, Nataliya F. A1 - Shainyan, Bagrat A. A1 - Schilde, Uwe A1 - Chipanina, Nina N. A1 - Oznobikhina, Larisa P. A1 - Albanov, Alexander I. A1 - Kleinpeter, Erich T1 - Synthesis, molecular structure, conformational analysis, and chemical properties of silicon-containing derivatives of quinolizidine JF - The journal of organic chemistry N2 - A silicon analog of quinolizidine 3,3,7,7-tetramethylhexahydro-1H-[1,4,2]oxazasilino[4,5-d][1,4,2]oxazasilin-9a-yl)methanol 3 was synthesized. X-ray diffraction analysis confirmed the trans configuration and low temperature NMR spectroscopy both the flexibility (barrier of interconversion 5.8 kcal mol(-1)) and the conformational equilibrium (chair-chair and chair-twist conformers) of the compound. The relative stability of the different isomers/conformers of 3 was calculated also at the MP2/6-311G(d,p) level of theory. Intra- and intermolecular hydrogen bonding in 3 and the appropriate equilibrium between free and self-associated molecules was studied in solvents of different polarity. Both the N-methyl quaternary ammonium salt and the O-trimethylsilyl derivative of 3 could be obtained and their structure determined. Y1 - 2012 U6 - https://doi.org/10.1021/jo202658n SN - 0022-3263 VL - 77 IS - 5 SP - 2382 EP - 2388 PB - American Chemical Society CY - Washington ER - TY - JOUR A1 - Najafpour, Mohammad Mahdi A1 - Hillier, Warwick A1 - Shamkhali, Amir Nasser A1 - Amini, Mojtaba A1 - Beckmann, Katrin A1 - Jaglicic, Zvonko A1 - Jagodic, Marko A1 - Strauch, Peter A1 - Moghaddam, Atefeh Nemati A1 - Beretta, Giangiacomo A1 - Bagherzadeh, Mojtaba T1 - Synthesis, characterization, DFT studies and catalytic activities of manganese(II) complex with 1,4-bis(2,2 ':6,2 ''-terpyridin-4 '-yl) benzene JF - Dalton transactions : a journal of inorganic chemistry, including bioinorganic, organometallic, and solid-state chemistry N2 - A new di-manganese complex with "back-to-back" 1,4-bis(2,2':6,2 ''-terpyridin-4'-yl) benzene ligation has been synthesized and characterised by a variety of techniques. The back-to-back ligation presents a novel new mononuclear manganese catalytic centre that functions as a heterogeneous catalysis for the evolution of oxygen in the presence of an exogenous oxidant. We discuss the synthesis and spectroscopic characterizations of this complex and propose a mechanism for oxygen evolution activity of the compound in the presence of oxone. The di-manganese complex also shows efficient and selective catalytic oxidation of sulfides in the presence of H2O2. Density functional theory calculations were used to assess the structural optimization of the complex and a proposed reaction pathway with oxone. The calculations show that middle benzene ring is distorted respect to both of metallic centers, and this in turn leads to negligible resonance of electrons between two sides of complex. The calculations also indicate the unpaired electron located on oxyl-ligand emphasizes the radical mechanism of water oxidation for the system. Y1 - 2012 U6 - https://doi.org/10.1039/c2dt31544k SN - 1477-9226 VL - 41 IS - 39 SP - 12282 EP - 12288 PB - Royal Society of Chemistry CY - Cambridge ER - TY - JOUR A1 - Kleinpeter, Erich A1 - Stojanovic, Milovan A1 - Markovic, Rade A1 - Baranac-Stojanovic, Marija T1 - Synthesis of thiazolidine-fused heterocycles via exo-mode cyclizations of vinylogous N-acyliminium ions N2 - Syntheses of thiazolidine-fused heterocycles via exo-mode cyclizations of vinylogous N-acyliminium ions incorporating heteroatom-based nucleophiles have been examined and discussed. The formation of (5,6)-membered systems was feasible with all nucleophiles tried (O, S and N), while the closing of the five-membered ring was restricted to O- and S-nucleophiles. The closure of a four-membered ring failed. Instead, the bicyclic (5,6)-membered acetal derivative and the tricyclic system with an eight-membered central ring were obtained from the substrates containing O and S nucleophilic moieties, respectively. The reaction outcome and stereochemistry are rationalized using quantum chemical calculations at B3LYP/6-31G(d) level. The exclusive cis-stereoselectivity in the formation of (5,6)- and (5,5)-membered systems results from thermodynamic control, whereas the formation of the eight-membered ring was kinetically controlled. Y1 - 2012 SN - 1477-0520 ER - TY - JOUR A1 - Stojanovic, Milovan A1 - Markovic, Rade A1 - Kleinpeter, Erich A1 - Baranac-Stojanovic, Marija T1 - Synthesis of thiazolidine-fused heterocycles via exo-mode cyclizations of vinylogous N-acyliminium ions JF - Organic & biomolecular chemistry : an international journal of synthetic, physical and biomolecular organic chemistry N2 - Syntheses of thiazolidine-fused heterocycles via exo-mode cyclizations of vinylogous N-acyliminium ions incorporating heteroatom-based nucleophiles have been examined and discussed. The formation of (5,6)-membered systems was feasible with all nucleophiles tried (O, S and N), while the closing of the five-membered ring was restricted to O- and S-nucleophiles. The closure of a four-membered ring failed. Instead, the bicyclic (5,6)-membered acetal derivative and the tricyclic system with an eight-membered central ring were obtained from the substrates containing O and S nucleophilic moieties, respectively. The reaction outcome and stereochemistry are rationalized using quantum chemical calculations at B3LYP/6-31G(d) level. The exclusive cis-stereoselectivity in the formation of (5,6)- and (5,5)-membered systems results from thermodynamic control, whereas the formation of the eight-membered ring was kinetically controlled. Y1 - 2012 U6 - https://doi.org/10.1039/c1ob06451g SN - 1477-0520 VL - 10 IS - 3 SP - 575 EP - 589 PB - Royal Society of Chemistry CY - Cambridge ER - TY - JOUR A1 - Kleinpeter, Erich A1 - Modarresi-Alam, Ali Reza A1 - Inaloo, Iman Dindarloo T1 - Synthesis of primary thiocarbamates by silica sulfuric acid as effective reagent under solid-state and solution conditions N2 - A simple and efficient method for the conversion of alcohols and phenols to primary O-thiocarbamates and S- thiocarbamates in the absence of solvent (solvent-free condition) using silica sulfuric acid (SiO2OSO3H) as a solid acid is described. The products are easily distinguished by IR, NMR and X-ray data. X-ray data of the compounds reveal a planar trigonal orientation of the NH2 nitrogen atom with the partial C,N double-bond character and the CS or CO groups in synperiplanar position with CarylO and CalkylS moieties, respectively. Moreover, the OCSNH2 group which is perpendicular to the plane of the benzene ring in 1c and the central thiocarbamate SCONH2 group in 2b are essentially planar. Y1 - 2012 SN - 0022-2860 ER - TY - JOUR A1 - Modarresi-Alam, Ali Reza A1 - Inaloo, Iman Dindarloo A1 - Kleinpeter, Erich T1 - Synthesis of primary thiocarbamates by silica sulfuric acid as effective reagent under solid-state and solution conditions JF - Journal of molecular structure N2 - A simple and efficient method for the conversion of alcohols and phenols to primary O-thiocarbamates and S-thiocarbamates in the absence of solvent (solvent-free condition) using silica sulfuric acid (equivalent to SiO2-OSO3H) as a solid acid is described. The products are easily distinguished by IR, NMR and X-ray data. X-ray data of the compounds reveal a planar trigonal orientation of the NH2 nitrogen atom with the partial C,N double-bond character and the C=S or C=O groups in synperiplanar position with C-aryl-O and C-alkyl-S moieties, respectively. Moreover, the -O-CS-NH2 group which is perpendicular to the plane of the benzene ring in 1c and the central thiocarbamate -S-CO-NH2 group in 2b are essentially planar. KW - Solvent-free KW - N-unsubstituted(primary)O-thiocarbamates KW - N-unsubstituted (primary)S-thiocarbamates KW - Isothiocyanic acid KW - Solid acid KW - Silica sulfuric acid Y1 - 2012 U6 - https://doi.org/10.1016/j.molstruc.2012.05.033 SN - 0022-2860 VL - 1024 IS - 9 SP - 156 EP - 162 PB - Elsevier CY - Amsterdam ER - TY - JOUR A1 - Goebel, Ronald A1 - Xie, Zai-Lai A1 - Neumann, Mike A1 - Günter, Christina A1 - Loebbicke, Ruben A1 - Kubo, Shiori A1 - Titirici, Maria-Magdalena A1 - Giordano, Cristina A1 - Taubert, Andreas T1 - Synthesis of mesoporous carbon/iron carbide hybrids with unusually high surface areas from the ionic liquid precursor [Bmim][FeCl4] JF - CrystEngComm N2 - Mesoporous carbon/iron carbide hybrid materials with surface areas reaching 800 m(2) g(-1) were synthesized via an exotemplating route using monolithic mesoporous silica as template and the ionic liquid 1-butyl-3-methylimidazolium tetrachloridoferrate(III) [Bmim][FeCl4] as carbon and iron source. After heat treatment (750 degrees C under argon) of the [Bmim][FeCl4] precursor confined within the silica matrix, the silica exotemplate was removed with HF leaving the mesoporous C/Fe3C hybrid behind. The surface areas and the pore sizes depend on the exotemplate and the surface areas a significantly larger than any other surface area reported for C/Fe3C hybrid materials so far. The approach is thus a prototype for the synthesis of high-surface area iron carbide-based hybrid materials with potential application in catalysis. Y1 - 2012 U6 - https://doi.org/10.1039/c2ce25064k SN - 1466-8033 VL - 14 IS - 15 SP - 4946 EP - 4951 PB - Royal Society of Chemistry CY - Cambridge ER - TY - JOUR A1 - Koeth, Anja A1 - Tiersch, Brigitte A1 - Appelhans, Dietmar A1 - Gradzielski, Michael A1 - Cölfen, Helmut A1 - Koetz, Joachim T1 - Synthesis of Core-Shell Gold Nanoparticles with Maltose-Modified Poly(Ethyleneimine) JF - Journal of dispersion science and technology N2 - The synthesis of ultrafine gold nanoparticles in presence of maltose-modified hyperbranched poly(ethyleneimines) (PEI) is described. The polymer acted as both a reducing and stabilising agent in the particle formation process. The nanoparticles were characterized by means of dynamic light scattering (DLS), transmission electron microscopy (TEM), analytical ultracentrifugation (AUC), small-angle x-ray scattering (SAXS), and small-angle neutron scattering (SANS). The mechanism of nanoparticle formation can be described in two steps. The reduction process of the Au3+ ions located in the inner coil region of the hyperbranched PEI led to the formation of a compact gold core, and is accompanied by a collapse of the polymer coil. Therefore, in the subsequent reduction process a gold-polymer hybrid shell is formed. By using the PEI of higher molar mass, core-shell gold nanoparticles of about 3.6 nm size with a more narrow size distribution and special fluorescence behavior could be synthesized. KW - Gold nanoparticles KW - gold-polymer hybrid shell KW - maltose-modified poly(ethyleneimine) Y1 - 2012 U6 - https://doi.org/10.1080/01932691.2010.530084 SN - 0193-2691 VL - 33 IS - 1-3 SP - 52 EP - 60 PB - Taylor & Francis Group CY - Philadelphia ER - TY - JOUR A1 - Schmidt, Bernd A1 - Krehl, Stefan A1 - Sotelo-Meza, Veronica T1 - Synthesis of chromanes through RCM-Transfer hydrogenation JF - Synthesis N2 - A sequential ruthenium-catalyzed ring-closing metathesis-transfer hydrogenation sequence has been established as a synthesis of chromanes starting from 2-(allyloxy)styrenes. The sequence requires only one precatalyst, the first-generation Grubbs catalyst, which is converted into a ruthenium hydride species in situ. Propan-2-ol serves as a chemical trigger for the formation of the ruthenium hydride and as hydrogen source. KW - ruthenium KW - chromanes KW - tandem reactions KW - metathesis KW - styrenes Y1 - 2012 U6 - https://doi.org/10.1055/s-0031-1289758 SN - 0039-7881 VL - 44 IS - 11 SP - 1603 EP - 1613 PB - Thieme CY - Stuttgart ER - TY - JOUR A1 - Schmidt, Bernd A1 - Krehl, Stefan A1 - Kelling, Alexandra A1 - Schilde, Uwe T1 - Synthesis of 8-Aryl-Substituted Coumarins based on Ring-Closing Metathesis and Suzuki-Miyaura coupling - synthesis of a Furyl Coumarin natural product from Galipea panamensis JF - The journal of organic chemistry N2 - The synthesis of 7-methoxy-8-(4-methyl-3-furyl)-2H-chromen-2-one, a natural product with antileishmanial activity recently isolated from the plant Galipea panamensis, is described. The key step is a Suzuki-Miyaura coupling of a furan-3-boronic acid and an 8-halocoumarin, which is advantageously synthesized using a ring-closing metathesis reaction. Several non-natural analogues are also available along these lines. Y1 - 2012 U6 - https://doi.org/10.1021/jo2026564 SN - 0022-3263 VL - 77 IS - 5 SP - 2360 EP - 2367 PB - American Chemical Society CY - Washington ER - TY - JOUR A1 - Bomm, Jana A1 - Günter, Christina A1 - Stumpe, Joachim T1 - Synthesis and optical characterization of thermosensitive, luminescent gold nanodots JF - The journal of physical chemistry : C, Nanomaterials and interfaces N2 - A facile one-pot synthesis for preparing thermosensitive, luminescent gold nanodots with diameters of 1-2 nm is presented. The influence of the alkyl chain length of the surface ligands (alkyl thiols) on the optical properties of the gold nanodots was investigated. The synthesized gold nanodots show strong thermosensitive photoluminescence. A photoluminescence quantum yield of 16.6% was observed at room temperature, which could be improved to a value of 28.6% when cooling the gold nanodot solutions to -7 degrees C. The synthesized thermosensitive, luminescent gold nanodots are interesting candidates for optoelectronic devices, medical imaging, sensing, or security labels. Y1 - 2012 U6 - https://doi.org/10.1021/jp206260r SN - 1932-7447 VL - 116 IS - 1 SP - 81 EP - 85 PB - American Chemical Society CY - Washington ER - TY - JOUR A1 - Kleinpeter, Erich A1 - Heydenreich, Matthias A1 - Koch, Andreas A1 - Linker, Torsten T1 - Synthesis and NMR spectroscopic conformational analysis of esters of 4-hydroxy-cyclohexanone-the more polar the molecule the more stable the axial conformer N2 - The esters of 4-hydroxy-cyclohexanone and a series of carboxylic acids R-COOH with R of different electronic and steric influence (R=Me, Et, n-Pr, i-Pr, n-Bu, i-Bu, sec-Bu, t-Bu, CF3, CH2Cl, CHCl2, CCl3, CH2Br, CHBr2, and CBr3) were synthesized and the conformational equilibria studied by 1H and 13C NMR spectroscopy at 103 K and at 295 K, respectively. The geometry of optimized structures of the axial/equatorial chair conformers was computed at the ab initio MO and DFT levels of theory. Only one preferred conformation was obtained for the axial and the equatorial conformer as well. When comparing the conformational equilibria of the cyclohexanone esters with those of the corresponding cyclohexyl esters a certain polarity contribution of the cyclohexanone framework was revealed, which is independent of the substituent effects and increases the stability of the axial conformers by a constant amount. Y1 - 2012 SN - 0040-4020 ER - TY - JOUR A1 - Kleinpeter, Erich A1 - Heydenreich, Matthias A1 - Koch, Andreas A1 - Linker, Torsten T1 - Synthesis and NMR spectroscopic conformational analysis of esters of 4-hydroxy-cyclohexanone-the more polar the molecule the more stable the axial conformer JF - Tetrahedron N2 - The esters of 4-hydroxy-cyclohexanone and a series of carboxylic acids R-COOH with R of different electronic and steric influence (R=Me, Et, n-Pr, i-Pr, n-Bu, i-Bu, sec-Bu, t-Bu, CF3, CH2Cl, CHCl2, CCl3, CH2Br, CHBr2, and CBr3) were synthesized and the conformational equilibria studied by H-1 and C-13 NMR spectroscopy at 103 K and at 295 K, respectively. The geometry of optimized structures of the axial 'equatorial chair conformers was computed at the ab initio MO and DFT levels of theory. Only one preferred conformation was obtained for the axial and the equatorial conformer as well. When comparing the conformational equilibria of the cyclohexanone esters with those of the corresponding cyclohexyl esters a certain polarity contribution of the cyclohexanone framework was revealed, which is independent of the substituent effects and increases the stability of the axial conformers by a constant amount. KW - 4-Substituted cyclohexanones KW - Conformational analysis KW - Dynamic NMR KW - Simulation of H-1 NMR spectra KW - Quantum chemical calculations KW - ALTONA equation Y1 - 2012 U6 - https://doi.org/10.1016/j.tet.2012.01.022 SN - 0040-4020 VL - 68 IS - 10 SP - 2363 EP - 2373 PB - Elsevier CY - Oxford ER - TY - JOUR A1 - Lazareva, Nataliya F. A1 - Albanov, Alexander I. A1 - Shainyan, Bagrat A. A1 - Kleinpeter, Erich T1 - Synthesis and conformational properties of substituted 1,4,2-oxazasilinanes: low temperature NMR study and quantum chemical calculations Y1 - 2012 UR - http://www.sciencedirect.com/science/article/pii/S0040402011018321 U6 - https://doi.org/10.1016/j.tet.2011.11.077 ER - TY - JOUR A1 - Lazareva, Nataliya F. A1 - Albanov, Alexander I. A1 - Shainyan, Bagrat A. A1 - Kleinpeter, Erich T1 - Synthesis and conformational properties of substituted 1,4,2-oxazasilinanes low temperature NMR study and quantum chemical calculations JF - Tetrahedron N2 - A number of N-substituted 2,2-dimethyl-1,4,2-oxazasilinanes 1 were synthesized and studied by variable temperature dynamic H-1 and C-13 NMR spectroscopy, room temperature N-15 NMR spectroscopy and theoretical calculations at the DFT and MP2 levels of theory. Both the preferred conformers were assigned and the barrier to the ring inversion of the saturated six-membered ring determined. From 1 the corresponding methyl iodide salts were produced, their structure studied by X-ray analysis and found to be in excellent agreement with the results of the theoretical calculations. KW - 1,4,2-Oxazasilinanes KW - Conformational analysis KW - Dynamic NMR KW - X-ray analysis KW - Quantum chemical calculations Y1 - 2012 U6 - https://doi.org/10.1016/j.tet.2011.11.077 SN - 0040-4020 VL - 68 IS - 4 SP - 1097 EP - 1104 PB - Elsevier CY - Oxford ER - TY - JOUR A1 - Shainyan, Bagrat A. A1 - Kirpichenko, Svetlana V. A1 - Kleinpeter, Erich T1 - Synthesis and conformational properties of 1,3-dimethyl-3-phenyl-1,3-azasilinane low temperature dynamic NMR and computational study JF - Arkivoc : free online journal of organic chemistry N2 - 1,3-Dimethyl-3-phenyl-1,3-azasilinane was synthesized and its conformational behavior was studied by the low temperature NMR spectroscopy and quantum chemical calculations. The compound was shown to exist as an equilibrium mixture of the PhaxMeeq and PheqMeax chair conformers with the N-methyl substituent in equatorial position. The barrier to ring inversion was also determined. KW - 1,3-Dimethyl-3-phenyl-1,3-azasilinane KW - conformational analysis KW - low temperature NMR spectroscopy KW - quantum chemical calculations Y1 - 2012 SN - 1551-7004 IS - 24 SP - 175 EP - 185 PB - ARKAT CY - Gainesville ER - TY - JOUR A1 - Kleinpeter, Erich A1 - Schainyan, Bagrat A. A1 - Kirpichenko, Svetlane V. T1 - Synthesis and conformational properties of 1,3-dimethyl-3-phenyl-1,3-azasilinane : low temperature dynamic NMR and computational study N2 - 1,3-Dimethyl-3-phenyl-1,3-azasilinane was synthesized and its conformational behavior was studied by the low temperature NMR spectroscopy and quantum chemical calculations. The compound was shown to exist as an equilibrium mixture of the PhaxMeeq and PheqMeax chair conformers with the N-methyl substituent in equatorial position. The barrier to ring inversion was also determined. Y1 - 2012 SN - 1551-7004 ER - TY - JOUR A1 - Shainyan, Bagrat A. A1 - Kirpichenko, Svetlana V. A1 - Kleinpeter, Erich T1 - Synthesis and conformational analysis of 1,3-azasilinanes JF - Tetrahedron N2 - 1-Isopropyl-3-methyl-3-phenyl-1,3-azasilinane 1 and 1-isopropyl-3,3-dimethyl-1,3-azasilinane 2 were synthesized and a detailed analysis of their NMR spectra, conformational equilibria and ring inversion processes is presented. Low temperature H-1/C-13 NMR spectroscopy, iteration of the H-1 NMR spectra and quantum chemical calculations showed slight predominance of the PheqMeax over the PhaxMeeq conformer of 1 at low temperature. The barrier for the chair to chair interconversion of both compounds was measured to be 8.25 kcal/mol. KW - 1,3-Azasilinanes KW - Conformational analysis KW - Dynamic NMR spectroscopy KW - Quantum chemical calculations KW - Ring current effect Y1 - 2012 U6 - https://doi.org/10.1016/j.tet.2012.05.106 SN - 0040-4020 VL - 68 IS - 36 SP - 7494 EP - 7501 PB - Elsevier CY - Oxford ER - TY - JOUR A1 - Melchert, Christian A1 - Yongvongsoontorn, Nunnarpas A1 - Behl, Marc A1 - Lendlein, Andreas T1 - Synthesis and characterization of telechelic oligoethers with terminal cinnamylidene acetic acid moieties JF - Journal of applied biomaterials & functional materials N2 - Purpose: The formation of photoresponsive hydrogels were reported by irradiation of star-shaped poly(ethylene glycol)s with terminal cinnamylidene acetic acid (CAA) groups, which are capable of a photoinduced [2+2] cycloaddition. In this study we explored whether oligo(ethylene glycol) s and oligo(propylene glycol)s of varying molecular architecture (linear or star-shaped) or molecular weights could be functionalized with CAA as terminal groups by esterification or by amide formation. Methods: Oligo(ethylene glycol) (OEG) and oligo(propylene glycol) (OPG) with varying molecular architecture (linear, star-shaped) and weight average molecular weights between 1000 and 5000 g.mol(-1) were functionalized by means of esterification of hydroxyl or amine endgroups with cinnamylidene acetic acid (CAA) or cinnamylidene acetyl chloride (CAC) as telechelic endgroups. The chemical structure, thermal properties, and molecular weights of the oligoethers obtained were determined by NMR spectroscopy, UV spectroscopy, DSC, and MALDI-TOF. Results: CAA-functionalized linear and star-shaped OEGs or OPGs could be obtained with a degree of functionalization higher than 90%. In MALDI-TOF measurements an increase in Mw of about 150 g.mol(-1) (for each terminal end) after the functionalization reaction was observed. OEGCAA and OPGCAA showed an increase in glass transition temperature (T-g) from about -70 degrees C to -50 degrees C, compared to the unfunctionalized oligoethers. In addition, the melting temperature (T-m) of OEGCAA decreased from about 55 C to 30 degrees C, which can be accounted for by the hampered crystallization of the precursors because of the bulky CAA end groups as well as by the loss of the hydroxyl telechelic end groups. Conclusion: The synthesis of photoresponsive oligoethers containing cinnamylidene acetic acid as telechelic endgroup was reported and high degrees of functionalization could be achieved. Such photosensitive oligomers are promising candidates as reactive precursors, for the preparation of biocompatible high molecular weight polymers and polymer networks. KW - Biocompatible polymers KW - Cinnamylidene acetic acid KW - Photoresponsive polymers Y1 - 2012 U6 - https://doi.org/10.5301/JABFM.2012.10364 SN - 2280-8000 VL - 10 IS - 3 SP - 185 EP - 190 PB - Wichtig CY - Milano ER - TY - JOUR A1 - Paz, Cristian A1 - Peter, Martin G. A1 - Schmidt, Bernd A1 - Becerra, Jose A1 - Gutierrez, Margarita A1 - Astudillo, Luis A1 - Silva, Mario T1 - Synthesis and AChE inhibiting activity of 2, 4 substituted 6-Phenyl Pyrimidines JF - Journal of the Chilean Chemical Society N2 - Novel substituted pyrimidines were synthesized from methyl 2,4-dioxo-4-phenyl-butanoate (I-A) and urea, followed by Mitsunobu coupling of I-A with benzyl or allyl alcohol to give the corresponding 2-hydroxypyrimidine ethers in good yields. Saponification of I-A, followed by reaction with benzyl or allyl amines in the presence of TBTU yielded 2-hydroxy-6-phenyl-pyrimidine 4-carboxamides. AChE and BuChE assays revealed 2-hydroxy-6-phenyl-pyrimidine-4-carboxyallyamide as the most active compound, IC50=90 mu M, with no inhibition of BuChE. KW - Pyrimidines KW - inhibition AChE KW - mitsunobu KW - TBTU Y1 - 2012 SN - 0717-9324 VL - 57 IS - 3 SP - 1292 EP - 1294 PB - Sociedad Chilena De Quimica CY - Concepcion ER - TY - JOUR A1 - Kleinpeter, Erich A1 - Csütörtöki, Renáta A1 - Szatmári, István A1 - Koch, Andreas A1 - Fulop, Ferenc T1 - Syntheses and conformational analyses of new naphth[1,2-e][1,3]oxazino[3,2-c]quinazolin-13-ones N2 - The syntheses of naphth[1,2-e][1,3]oxazino[3,2-c]quinazolin-13-one derivatives (3a-f) were achieved by the solvent-free heating of benzyloxycarbonyl-protected intermediates (2a-f) with MeONa. For intermediates 2a-f, prepared by the reactions of substituted aminonaphthols with benzyl N-(2-formylphenyl)carbamate, not only the expected trans ring form B and chain form A1, but also the rearranged chain form A2 as a new tautomer were detected in DMSO at room temperature. The quantity of A2 in the tautomeric mixture was changed with time. Conformational analyses of the target heterocycles 3a-f by NMR spectroscopy and accompanying theoretical calculations at the DFT level of theory revealed that the oxazine ring preferred a twisted chair conformation and the quinazolone ring was planar. Besides the conformations, both the configurations at C-7a and C-15 and the preferred rotamers of the 1-naphthyl substituent at C-15 were assigned, which allowed evaluation of the aryl substituent-dependent steric hindrance in this part of the molecules. Configurational assignments were corroborated by quantifying the ring current effect of 15-aryl in terms of spatial NICS. Y1 - 2012 ER - TY - JOUR A1 - Csütörtöki, Renata A1 - Szatmari, Istvan A1 - Koch, Andreas A1 - Heydenreich, Matthias A1 - Kleinpeter, Erich A1 - Fulop, Ferenc T1 - Syntheses and conformational analyses of new naphth[1,2-e][1,3]oxazino[3,2-c] quinazolin-13-ones JF - Tetrahedron N2 - The syntheses of naphth[1,2-e][1,3]oxazino[3,2-c]quinazolin-13-one derivatives (3a-f) were achieved by the solvent-free heating of benzyloxycarbonyl-protected intermediates (2a-f) with MeONa. For intermediates 2a-f, prepared by the reactions of substituted aminonaphthols with benzyl N-(2-formylphenyl)carbamate, not only the expected trans ring form B and chain form A(1), but also the rearranged chain form A(2) as a new tautomer were detected in DMSO at room temperature. The quantity of A(2) in the tautomeric mixture was changed with time. Conformational analyses of the target heterocycles 3a-f by NMR spectroscopy and accompanying theoretical calculations at the DFT level of theory revealed that the oxazine ring preferred a twisted chair conformation and the quinazolone ring was planar. Besides the conformations, both the configurations at C-7a and C-15 and the preferred rotamers of the 1-naphthyl substituent at C-15 were assigned, which allowed evaluation of the aryl substituent-dependent steric hindrance in this part of the molecules. Configurational assignments were corroborated by quantifying the ring current effect of 15-aryl in terms of spatial NICS. KW - Naphthoxazinoquinazolinones KW - Aminonaphthols KW - NMR spectroscopy KW - Conformational analysis KW - Theoretical calculations KW - Ring current effect Y1 - 2012 U6 - https://doi.org/10.1016/j.tet.2012.04.026 SN - 0040-4020 VL - 68 IS - 24 SP - 4600 EP - 4608 PB - Elsevier CY - Oxford ER - TY - JOUR A1 - Risse, Sebastian A1 - Kussmaul, Bjoern A1 - Krüger, Hartmut A1 - Kofod, Guggi T1 - Synergistic improvement of actuation properties with compatibilized high permittivity filler JF - Advanced functional materials N2 - Electroactive polymers can be used for actuators with many desirable features, including high electromechanical energy density, low weight, compactness, direct voltage control, and complete silence during actuation. These features may enable personalized robotics with much higher ability to delicately manipulate their surroundings than can be achieved with currently available actuators; however, much work is still necessary to enhance the electroactive materials. Electric field-driven actuator materials are improved by an increase in permittivity and by a reduction in stiffness. Here, a synergistic enhancement method based on a macromolecular plasticizing filler molecule with a combination of both high dipole moment and compatibilizer moieties, synthesized to simultaneously ensure improvement of electromechanical properties and compatibility with the host matrix is presented. Measurements show an 85% increase in permittivity combined with 290% reduction in mechanical stiffness. NMR measurements confirm the structure of the filler while DSC measurements confirm that it is compatible with the host matrix at all the mixture ratios investigated. Actuation strain measurements in the pure shear configuration display an increase in sensitivity to the electrical field of more than 450%, confirming that the filler molecule does not only improve dielectric and mechanical properties, it also leads to a synergistic enhancement of actuation properties by simple means. KW - allycyanide KW - silicone-based dielectric elastomer actuators KW - permittivity enhancement KW - compatibilized filler molecules Y1 - 2012 U6 - https://doi.org/10.1002/adfm.201200320 SN - 1616-301X VL - 22 IS - 18 SP - 3958 EP - 3962 PB - Wiley-VCH CY - Weinheim ER - TY - JOUR A1 - Navirian, H. A1 - Shayduk, R. A1 - Leitenberger, Wolfram A1 - Goldshteyn, J. A1 - Gaal, P. A1 - Bargheer, Matias T1 - Synchrotron-based ultrafast x-ray diffraction at high repetition rates JF - Review of scientific instruments : a monthly journal devoted to scientific instruments, apparatus, and techniques N2 - We present a setup for ultrafast x-ray diffraction (UXRD) based at the storage ring BESSY II, in particular, a pump laser that excites the sample using 250 fs laser-pulses at repetition rates ranging from 208 kHz to 1.25 MHz. We discuss issues connected to the high heat-load and spatio-temporal alignment strategies in the context of a UXRD experiment at high repetition rates. The spatial overlap between laser pump and x-ray probe pulse is obtained with 10 mu m precision and transient lattice changes can be recorded with an accuracy of delta a/a(0) = 10(-6). We also compare time-resolved x-ray diffraction signals from a laser excited LSMO/STO superlattice with phonon dynamics simulations. From the analysis we determine the x-ray pulse duration to 120 ps in standard operation mode and below 10 ps in low-alpha mode. Y1 - 2012 U6 - https://doi.org/10.1063/1.4727872 SN - 0034-6748 VL - 83 IS - 6 PB - American Institute of Physics CY - Melville ER - TY - JOUR A1 - Zhong, Qi A1 - Metwalli, Ezzeldin A1 - Kaune, Gunar A1 - Rawolle, Monika A1 - Bivigou Koumba, Achille Mayelle A1 - Laschewsky, André A1 - Papadakis, Christine M. A1 - Cubitt, Robert A1 - Müller-Buschbaum, Peter T1 - Switching kinetics of thin thermo-responsive hydrogel films of poly(monomethoxy-diethyleneglycol-acrylate) probed with in situ neutron reflectivity JF - Soft matter N2 - The switching kinetics of thin thermo-responsive hydrogel films of poly(monomethoxy-diethyleneglycol-acrylate) (PMDEGA) are investigated. Homogeneous and smooth PMDEGA films with a thickness of 35.9 nm are prepared on silicon substrates by spin coating. As probed with white light interferometry, PMDEGA films with a thickness of 35.9 nm exhibit a phase transition temperature of the lower critical solution temperature (LCST) type of 40 degrees C. In situ neutron reflectivity is performed to investigate the thermo-responsive behavior of these PMDEGA hydrogel films in response to a sudden thermal stimulus in deuterated water vapor atmosphere. The collapse transition proceeds in a complex way which can be seen as three steps. The first step is the shrinkage of the initially swollen film by a release of water. In the second step the thickness remains constant with water molecules embedded in the film. In the third step, perhaps due to a conformational rearrangement of the collapsed PMDEGA chains, water is reabsorbed from the vapor atmosphere, thereby giving rise to a relaxation process. Both the shrinkage and relaxation processes can be described by a simple model of hydrogel deswelling. Y1 - 2012 U6 - https://doi.org/10.1039/c2sm25401h SN - 1744-683X VL - 8 IS - 19 SP - 5241 EP - 5249 PB - Royal Society of Chemistry CY - Cambridge ER - TY - THES A1 - Lohmann, Dirk T1 - Sustainable management of semi-arid African savannas under environmental and political change T1 - Nachhaltige Nutzung semiarider Savannen in Afrika unter dem Einfluss von klimatischem und politischem Wandel N2 - Drylands cover about 40% of the earth’s land surface and provide the basis for the livelihoods of 38% of the global human population. Worldwide, these ecosystems are prone to heavy degradation. Increasing levels of dryland degradation result a strong decline of ecosystem services. In addition, in highly variable semi-arid environments changing future environmental conditions will potentially have severe consequences for productivity and ecosystem dynamics. Hence, global efforts have to be made to understand the particular causes and consequences of dryland degradation and to promote sustainable management options for semi-arid and arid ecosystems in a changing world. Here I particularly address the problem of semi-arid savanna degradation, which mostly occurs in form of woody plant encroachment. At this, I aim at finding viable sustainable management strategies and improving the general understanding of semi-arid savanna vegetation dynamics under conditions of extensive livestock production. Moreover, the influence of external forces, i.e. environmental change and land reform, on the use of savanna vegetation and on the ecosystem response to this land use is assessed. Based on this I identify conditions and strategies that facilitate a sustainable use of semi-arid savanna rangelands in a changing world. I extended an eco-hydrological model to simulate rangeland vegetation dynamics for a typical semi-arid savanna in eastern Namibia. In particular, I identified the response of semi-arid savanna vegetation to different land use strategies (including fire management) also with regard to different predicted precipitation, temperature and CO2 regimes. Not only environmental but also economic and political constraints like e.g. land reform programmes are shaping rangeland management strategies. Hence, I aimed at understanding the effects of the ongoing process of land reform in southern Africa on land use and the semi-arid savanna vegetation. Therefore, I developed and implemented an agent-based ecological-economic modelling tool for interactive role plays with land users. This tool was applied in an interdisciplinary empirical study to identify general patterns of management decisions and the between-farm cooperation of land reform beneficiaries in eastern Namibia. The eco-hydrological simulations revealed that the future dynamics of semi-arid savanna vegetation strongly depend on the respective climate change scenario. In particular, I found that the capacity of the system to sustain domestic livestock production will strongly depend on changes in the amount and temporal distribution of precipitation. In addition, my simulations revealed that shrub encroachment will become less likely under future climatic conditions although positive effects of CO2 on woody plant growth and transpiration have been considered. While earlier studies predicted a further increase in shrub encroachment due to increased levels of atmospheric CO2, my contrary finding is based on the negative impacts of temperature increase on the drought sensitive seedling germination and establishment of woody plant species. Further simulation experiments revealed that prescribed fires are an efficient tool for semi-arid rangeland management, since they suppress woody plant seedling establishment. The strategies tested have increased the long term productivity of the savanna in terms of livestock production and decreased the risk for shrub encroachment (i.e. savanna degradation). This finding refutes the views promoted by existing studies, which state that fires are of minor importance for the vegetation dynamics of semi-arid and arid savannas. Again, the difference in predictions is related to the bottleneck at the seedling establishment stage of woody plants, which has not been sufficiently considered in earlier studies. The ecological-economic role plays with Namibian land reform beneficiaries showed that the farmers made their decisions with regard to herd size adjustments according to economic but not according to environmental variables. Hence, they do not manage opportunistically by tracking grass biomass availability but rather apply conservative management strategies with low stocking rates. This implies that under the given circumstances the management of these farmers will not per se cause (or further worsen) the problem of savanna degradation and shrub encroachment due to overgrazing. However, as my results indicate that this management strategy is rather based on high financial pressure, it is not an indicator for successful rangeland management. Rather, farmers struggle hard to make any positive revenue from their farming business and the success of the Namibian land reform is currently disputable. The role-plays also revealed that cooperation between farmers is difficult even though obligatory due to the often small farm sizes. I thus propose that cooperation needs to be facilitated to improve the success of land reform beneficiaries. N2 - Semiaride (halbtrockene) Savannen bedecken große Teile der Erdoberfläche und sichern die Lebensgrundlage von vielen Millionen Menschen. Die häufigste Form der Landnutzung in diesen Trockengebieten ist die Produktion von Vieh in extensiver Weidelandbewirtschaftung. In Folge klimatischer Veränderungen und als Konsequenz aus der teils intensiven Beweidung dieser Trockengebiete kommt es häufig zur Degradierung derselben in Form einer Zunahme von ‚unerwünschter‘ holziger Vegetation auf Kosten von futterverwertbaren Gräsern. Dieser als Verbuschung bezeichnete Prozess hat schwere negative Auswirkungen auf die betroffenen Ökosysteme und ist die Ursache für einen zunehmenden Rückgang der ökonomischen Leistungsfähigkeit der betroffenen Betriebe. In meiner Dissertation befasse ich mich mit den Auswirkungen von Klimawandel und politischen Veränderungen auf die Savannenvegetation im südlichen Afrika und auf die Möglichkeiten für die Nutzung dieser Ökosysteme in Form von Viehwirtschaft. Hierbei möchte ich sowohl das allgemeine Verständnis der ökologischen Zusammenhänge verbessern, als auch Strategien für die nachhaltige Nutzung der Savannen identifizieren und bewerten. Da nicht nur ökologische, sondern auch ökonomische und politische Einflussfaktoren, wie zum Beispiel die umfangreichen Landumverteilungen im Rahmen der Bodenreform im südlichen Afrika auf die tatsächliche Landnutzung wirken, habe ich im Rahmen der Dissertation zudem untersucht, nach welchen Umwelt und Kapitalvariablen sich die Farmer, welche Ihr Land im Rahmen der Bodenreform zugeteilt bekommen haben, bei Ihren Entscheidungen richten. Methodisch verwende ich verschiedene Simulationsmodelle, welche zur Untersuchung der langfristigen Veränderungen von verschiedensten Szenarien (Klimawandel, Landnutzung) geeignet sind. Hierbei habe ich teilweise bestehende Modelle angepasst, aber auch ein neues Modell, welches zur Befragung von Farmern in Namibia verwendet wurde, entwickelt. Meine Dissertation führt im Wesentlichen zu vier Erkenntnissen: Erstens, zeigen meine Ergebnisse, welche große Bedeutung die spezifischen ökologischen Eigenschaften der Bäume und Sträucher in semiariden Savannen für die Vorhersage der Entwicklung dieser Systeme unter Klimawandel hat. Hierbei zeigte sich, dass insbesondere die Sensitivität der Keimlinge gegenüber Trockenheit und Feuer eine entscheidende Rolle spielt. Daraus folgt die zweite wesentliche Erkenntnis: Feuer eignet sich in herausragender Weise, um halbtrockene Savannen vor der Verbuschung zu bewahren. Drittens haben die Rollenspiele mit Farmern in Namibia gezeigt, dass deren Entscheidungen im Wesentlichen von finanziellen Schwierigkeiten und nicht von Umwelteinflüssen getrieben werden. Dennoch zeigten meine Ergebnisse, dass diese Farmer mit Ihrem derzeitigen Verhalten wahrscheinlich nicht zur weiteren Degradierung der Savannenvegetation beitragen. Die vierte, und mit am bedeutendste Erkenntnis aus meiner Arbeit ist, dass konservative Beweidungsstrategien mit geringen und konstanten Viehdichten notwendig sind um semiaride Savannen dauerhaft in ökologisch und ökonomisch nachhaltiger Weise zu Nutzen. KW - Savanne KW - nachhaltige Landnutzung KW - ökohydrologische Modellierung KW - Land Reform KW - Klimawandel KW - Savanna KW - sustainable land use KW - eco-hydrological modelling KW - land reform KW - climate change Y1 - 2012 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-65069 ER - TY - THES A1 - Falco, Camillo T1 - Sustainable biomass-derived hydrothermal carbons for energy applications T1 - Nachhaltiger, Biomasse-basierter Hydrothermalkohlenstoff für Energieanwendungen N2 - The need to reduce humankind reliance on fossil fuels by exploiting sustainably the planet renewable resources is a major driving force determining the focus of modern material research. For this reason great interest is nowadays focused on finding alternatives to fossil fuels derived products/materials. For the short term the most promising substitute is undoubtedly biomass, since it is the only renewable and sustainable alternative to fossil fuels as carbon source. As a consequence efforts, aimed at finding new synthetic approaches to convert biomass and its derivatives into carbon-based materials, are constantly increasing. In this regard, hydrothermal carbonisation (HTC) has shown to be an effective means of conversion of biomass-derived precursors into functional carbon materials. However the attempts to convert raw biomass, in particular lignocellulosic one, directly into such products have certainly been rarer. Unlocking the direct use of these raw materials as carbon precursors would definitely be beneficial in terms of HTC sustainability. For this reason, in this thesis the HTC of carbohydrate and protein-rich biomass was systematically investigated, in order to obtain more insights on the potentials of this thermochemical processing technique in relation to the production of functional carbon materials from crude biomass. First a detailed investigation on the HTC conversion mechanism of lignocellulosic biomass and its single components (i.e. cellulose, lignin) was developed based on a comparison with glucose HTC, which was adopted as a reference model. In the glucose case it was demonstrated that varying the HTC temperature allowed tuning the chemical structure of the synthesised carbon materials from a highly cross-linked furan-based structure (T = 180oC) to a carbon framework composed of polyaromatic arene-like domains. When cellulose or lignocellulosic biomass was used as carbon precursor, the furan rich structure could not be isolated at any of the investigated processing conditions. These evidences were indicative of a different HTC conversion mechanism for cellulose, involving reactions that are commonly observed during pyrolytic processes. The evolution of glucose-derived HTC carbon chemical structure upon pyrolysis was also investigated. These studies revealed that upon heat treatment (Investigated temperatures 350 – 900 oC) the furan-based structure was progressively converted into highly curved aromatic pre-graphenic domains. This thermal degradation process was observed to produce an increasingly more hydrophobic surface and considerable microporosity within the HTC carbon structure. In order to introduce porosity in the HTC carbons derived from lignocellulosic biomass, KOH chemical activation was investigated as an HTC post-synthesis functionalisation step. These studies demonstrated that HTC carbons are excellent precursors for the production of highly microporous activated carbons (ACs) and that the porosity development upon KOH chemical activation is dependent on the chemical structure of the HTC carbon, tuned by employing different HTC temperatures. Preliminary testing of the ACs for CO2 capture or high pressure CH4 storage yielded very promising results, since the measured uptakes of both adsorbates (i.e. CO2 and CH4) were comparable to top-performing and commercially available adsorbents, usually employed for these end-applications. The combined use of HTC and KOH chemical activation was also employed to produce highly microporous N-doped ACs from microalgae. The hydrothermal treatment of the microalgae substrate was observed to cause the depletion of the protein and carbohydrate fractions and the near complete loss (i.e. 90%) of the microalgae N-content, as liquid hydrolysis/degradation products. The obtained carbonaceous product showed a predominantly aliphatic character indicating the presence of alkyl chains presumably derived from the lipid fractions. Addition of glucose to the initial reaction mixture was found out to be extremely beneficial, because it allowed the fixation of a higher N amount, in the algae derived HTC carbons (i.e.  60%), and the attainment of higher product yields (50%). Both positive effects were attributed to Maillard type cascade reactions taking place between the monosaccharides and the microalgae derived liquid hydrolysis/degradation products, which were in this way recovered from the liquid phase. KOH chemical activation of the microalgae/glucose mixture derived HTC carbons produced highly microporous N-doped carbons. Although the activation process led to a major reduction of the N-content, the retained N-amount in the ACs was still considerable. These features render these materials ideal candidates for supercapacitors electrodes, since they provide extremely high surface areas, for the formation of electric double-layer, coupled to abundant heteroatom doping (i.e. N and O) necessary to obtain a pseudocapacitance contribution. N2 - Die Notwendigkeit, die Abhängigkeit der Menschheit von fossilen Brennstoffen zu reduzieren ist die treibende Kraft hinter aktuellen Forschungsanstrengungen in den Materialwissenschaften. Folglich besteht heutzutage ein erhebliches Interesse daran Alternativen zu Materialien, die aus fossilen Resourcen gewonnen werden, zu finden. Kurzfristig ist zweifellos Biomasse die vielversprechendste Alternative, da sie aus heutiger Sicht die einzige nicht-fossile, nachhaltige und nachwachsende Kohlenstoffquelle ist. Konsequenterweise werden die Antrengungen neue Syntheseansätze zur Konvertierung von Biomasse und ihren Derivaten in kohlenstoffbasierten Materialien forwährend erhöht. In diesem Zusammenhang hat sich die Hydrothermalkarbonisierung (HTC) als sehr vielseitiges Werkzeug zur Konvertierung von Biomasse-basierten Ausgangsstoffen in funktionale Kohlenstoffmaterialien herausgestellt. Dennoch gibt es bisher wenige Ansätze um rohe Biomasse, genauer gesagt Lignicellulose, direkt in funktionale Materialien umzusetzen. Könnte der direkte Einsatz von roher Biomasse Verfahren wie der HTC zugänglich gemacht werden, würde dies die Nachhaltigkeit des Verfahrens immens steigern. Daher wurde in dieser Dissertation die Hydrothermalkarbonisierung von kohlenhydratreicher (d. h. Lignicelluse) und proteinreicher (d. h. Microalgae) Biomasse systematisch analysiert. Diese Untersuchung galt dem Ziel einen besseren Einblick in das Potential dieser thermochemischen Verarbeitungsmethode funktionale Kohlenstoffmaterialien aus unverarbeiteter Biomasse hervorzubringen zu gewinnen. Die hergestellten Materialien wurden mittels chemischer Aktivierung nachträglich weiter behandelt. Dieser zusätzliche Verarbeitungsschritt ermöglichte die Herstellung hochporöser aktiverter Kohlenstoffe (AC). Die aus Lignicellulose gewonnenen ACs zeigten exzellente Eigenschaften bei der Aufnahme von CO2 und der Hochdruckspeicherung von CH4 währen die aus Microalgae gewonnen Eigenschaften an den Tag legten (z. B. hohe Oberfläche und N-Dotierung), welche sie zu vielversprechenden Materialien für Superkondensatoren machen. Die in dieser Dissertation präsentierte Arbeit zeigte außergewöhnliche Fortschritte in Richtung der Anwendung von unbehandelter Biomasse als Ausgangsmaterial für die Produktion von funktionalen Kohlenstoffen. KW - Biomasse KW - Kohlenmaterialien KW - Grüne Chemie KW - Nachhaltigkeit KW - Enegieanwendungen KW - Biomass KW - Carbon materials KW - Green Chemistry KW - Sustainability KW - Energy Applications Y1 - 2012 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-59785 ER - TY - JOUR A1 - Horovitz, Baruch A1 - Henkel, Carsten T1 - Surface plasmons at composite surfaces with diffusive charges JF - epl : a letters journal exploring the frontiers of physics N2 - Metal surfaces with disorder or with nanostructure modifications are studied, allowing for a localized charge layer (CL) in addition to continuous charges (CC) in the bulk, both charges having a compressional or diffusive nonlocal response. The notorious problem of "additional boundary conditions" is resolved with the help of a Boltzmann equation that involves the scattering between the two charge types. Depending on the strength of this scattering, the oscillating charges can be dominantly CC or CL; the surface plasmon (SP) resonance acquires then a relatively small linewidth, in agreement with a large set of data. With a few parameters our model describes a large variety of SP dispersions corresponding to observed data. Y1 - 2012 U6 - https://doi.org/10.1209/0295-5075/97/57010 SN - 0295-5075 VL - 97 IS - 5 PB - EDP Sciences CY - Mulhouse ER - TY - JOUR A1 - König, Tobias A1 - Sekhar, Y. Nataraja A1 - Santer, Svetlana T1 - Surface plasmon nanolithography impact of dynamically varying near-field boundary conditions at the air-polymer interface JF - Journal of materials chemistry N2 - It is well-known that surface plasmon generated near fields of suitably irradiated metal nano-structures can induce a patterning in an azobenzene-modified photosensitive polymer film placed on top. The change in the topography usually follows closely and permanently the underlying near field intensity pattern. With this approach, one can achieve a multitude of morphologies by additionally changing light intensity, polarization and the kind of metal used for nano-structuring. In this paper, we demonstrate that below a critical value of the polymer film thickness, the receding polymer material induces a change in refractive index of the glass-metal-polymer system, modifying the near field intensity distribution and causing a back-reaction on the flow of polymer material. This has a profound influence on the smallest size of topographical features that can be imprinted into the polymer. Y1 - 2012 U6 - https://doi.org/10.1039/c2jm15864g SN - 0959-9428 VL - 22 IS - 13 SP - 5945 EP - 5950 PB - Royal Society of Chemistry CY - Cambridge ER - TY - JOUR A1 - Floss, Gereon A1 - Granucci, Giovanni A1 - Saalfrank, Peter T1 - Surface hopping dynamics of direct trans -> cis photoswitching of an azobenzene derivative in constrained adsorbate geometries JF - The journal of chemical physics : bridges a gap between journals of physics and journals of chemistr N2 - With ongoing miniaturization of electronic devices, the need for individually addressable, switchable molecules arises. An example are azobenzenes on surfaces which have been shown to be switchable between trans and cis forms. Here, we examine the "direct" (rather than substrate-mediated) channel of the trans -> cis photoisomerization after pi pi* excitation of tetra-tert-butyl-azobenzene physisorbed on surfaces mimicking Au(111) and Bi(111), respectively. In spirit of the direct channel, the electronic structure of the surface is neglected, the latter merely acting as a rigid platform which weakly interacts with the molecule via Van-der-Waals forces. Starting from thermal ensembles which represent the trans-form, sudden excitations promote the molecules to pi pi*-excited states which are non-adiabatically coupled among themselves and to a n pi*-excited and the ground state, respectively. After excitation, relaxation to the ground state by internal conversion takes place, possibly accompanied by isomerization. The process is described here by "on the fly" semiclassical surface hopping dynamics in conjunction with a semiempirical Hamiltonian (AM1) and configuration-interaction type methods. It is found that steric constraints imposed by the substrate lead to reduced but non-vanishing, trans -> cis reaction yields and longer internal conversion times than for the isolated molecule. Implications for recent experiments for azobenzenes on surfaces are discussed. KW - AM1 calculations KW - bismuth KW - configuration interactions KW - excited states KW - gold KW - isomerisation KW - organic compounds KW - photochemistry KW - van der Waals forces Y1 - 2012 U6 - https://doi.org/10.1063/1.4769087 SN - 0021-9606 VL - 137 IS - 23 PB - American Institute of Physics CY - Melville ER - TY - JOUR A1 - Lange, Maik A1 - Braune, Steffen A1 - Luetzow, Karola A1 - Richau, Klaus A1 - Scharnagl, Nico A1 - Weinhart, Marie A1 - Neffe, Axel T. A1 - Jung, Friedrich A1 - Haag, Rainer A1 - Lendlein, Andreas T1 - Surface functionalization of poly(ether imide) membranes with linear, methylated oligoglycerols for reducing thrombogenicity JF - Macromolecular rapid communications N2 - Materials for biomedical applications are often chosen for their bulk properties. Other requirements such as a hemocompatible surface shall be fulfilled by suitable chemical functionalization. Here we show, that linear, side-chain methylated oligoglycerols (OGMe) are more stable to oxidation than oligo(ethylene glycol) (OEG). Poly(ether imide) (PEI) membranes functionalized with OGMes perform at least as good as, and partially better than, OEG functionalized PEI membranes in view of protein resistance as well as thrombocyte adhesion and activation. Therefore, OGMes are highly potent surface functionalizing molecules for improving the hemocompatibility of polymers. KW - hemocompatibility KW - poly(ethylene glycol) KW - polyglycerol KW - polyimides KW - surface chemistry Y1 - 2012 U6 - https://doi.org/10.1002/marc.201200426 SN - 1022-1336 VL - 33 IS - 17 SP - 1487 EP - 1492 PB - Wiley-VCH CY - Weinheim ER - TY - JOUR A1 - Schildgen, Taylor F. A1 - Cosentino, D. A1 - Caruso, A. A1 - Buchwaldt, Robert A1 - Yildirim, C. A1 - Bowring, S. A. A1 - Rojay, B. A1 - Echtler, Helmut Peter A1 - Strecker, Manfred T1 - Surface expression of eastern Mediterranean slab dynamics: Neogene topographic and structural evolution of the southwest margin of the Central Anatolian Plateau, Turkey JF - TECTONICS N2 - The southwest margin of the Central Anatolian Plateau has experienced multiple phases of topographic growth, including the formation of localized highs prior to the Late Miocene that were later affected by wholesale uplift of the plateau margin. Our new biostratigraphic data limit the age of uplifted marine sediments at the southwest plateau margin at 1.5 km elevation to <7.17 Ma, and regional lithostratigraphic correlations imply that the age is <6.7 Ma. Single-grain CA-TIMS U-Pb zircon analyses from a reworked ash within the marine sediments yield dates as young as 10.6 Ma, indicating a maximum age that is consistent with the biostratigraphy. Our structural measurements within the uplifted region and fault inversion modeling agree with previous findings in surrounding regions, with early contraction followed by strike-slip and extensional deformation during uplift. Focal mechanisms from shallow earthquakes show that the extensional phase has continued to the present. Broad similarities in the change in the tectonic stress regime (after 8 Ma) and the onset of surface uplift (after 7 Ma) imply that deep-seated process(es) caused post-7 Ma uplift. The geometry of lithospheric slabs beneath the plateau margin, Pliocene to recent alkaline volcanism, and the uplift pattern with accompanying normal faulting point toward slab tearing and localized heating at the base of the lithosphere as a probable mechanism for post-7 Ma uplift of the southwest margin. Considering previous work in the region, there appears to be an important link between slab dynamics and surface uplift throughout the Anatolian Plateau’s southern margin. Y1 - 2012 U6 - https://doi.org/10.1029/2011TC003021 SN - 0278-7407 SN - 1944-9194 VL - 31 PB - AMER GEOPHYSICAL UNION CY - WASHINGTON ER - TY - JOUR A1 - Ellis, S. C. A1 - Bland-Hawthorn, Joss A1 - Lawrence, J. A1 - Horton, A. J. A1 - Trinh, C. A1 - Leon-Saval, S. G. A1 - Shortridge, K. A1 - Bryant, J. A1 - Case, S. A1 - Colless, M. A1 - Couch, W. A1 - Freeman, K. A1 - Gers, L. A1 - Glazebrook, K. A1 - Haynes, R. A1 - Lee, S. A1 - Löhmannsröben, Hans-Gerd A1 - O'Byrne, J. A1 - Miziarski, S. A1 - Roth, M. A1 - Schmidt, B. A1 - Tinney, C. G. A1 - Zheng, J. T1 - Suppression of the near-infrared OH night-sky lines with fibre Bragg gratings - first results JF - Monthly notices of the Royal Astronomical Society N2 - The background noise between 1 and 1.8 ?mu m in ground-based instruments is dominated by atmospheric emission from hydroxyl molecules. We have built and commissioned a new instrument, the Gemini Near-infrared OH Suppression Integral Field Unit (IFU) System (GNOSIS), which suppresses 103 OH doublets between 1.47 and 1.7?mu m by a factor of 1000 with a resolving power of 10?000. We present the first results from the commissioning of GNOSIS using the IRIS2 spectrograph at the Anglo-Australian Telescope. We present measurements of sensitivity, background and throughput. The combined throughput of the GNOSIS fore-optics, grating unit and relay optics is 36?per cent, but this could be improved to 46?per cent with a more optimal design. We measure strong suppression of the OH lines, confirming that OH suppression with fibre Bragg gratings will be a powerful technology for low-resolution spectroscopy. The integrated OH suppressed background between 1.5 and 1.7 mu m is reduced by a factor of 9 compared to a control spectrum using the same system without suppression. The potential of low-resolution OH-suppressed spectroscopy is illustrated with example observations of Seyfert galaxies and a low-mass star. The GNOSIS background is dominated by detector dark current below 1.67 mu m and by thermal emission above 1.67 mu m. After subtracting these, we detect an unidentified residual interline component of 860 +/- 210 photons s-1 m-2?arcsec-2?mu m-1, comparable to previous measurements. This component is equally bright in the suppressed and control spectra. We have investigated the possible source of the interline component, but were unable to discriminate between a possible instrumental artefact and intrinsic atmospheric emission. Resolving the source of this emission is crucial for the design of fully optimized OH suppression spectrographs. The next-generation OH suppression spectrograph will be focused on resolving the source of the interline component, taking advantage of better optimization for a fibre Bragg grating feed incorporating refinements of design based on our findings from GNOSIS. We quantify the necessary improvements for an optimal OH suppressing fibre spectrograph design. KW - atmospheric effects KW - instrumentation: miscellaneous KW - infrared: general Y1 - 2012 U6 - https://doi.org/10.1111/j.1365-2966.2012.21602.x SN - 0035-8711 VL - 425 IS - 3 SP - 1682 EP - 1695 PB - Wiley-Blackwell CY - Hoboken ER - TY - JOUR A1 - Quasthoff, Matthias A1 - Meinel, Christoph T1 - Supporting object-oriented programming of semantic-web software JF - IEEE transactions on systems, man, and cybernetics : Part C, Applications and reviews N2 - This paper presents the state of the art in the development of Semantic-Web-enabled software using object-oriented programming languages. Object triple mapping (OTM) is a frequently used method to simplify the development of such software. A case study that is based on interviews with developers of OTM frameworks is presented at the core of this paper. Following the results of the case study, the formalization of OTM is kept separate from optional but desirable extensions of OTM with regard to metadata, schema matching, and integration into the Semantic-Web infrastructure. The material that is presented is expected to not only explain the development of Semantic-Web software by the usage of OTM, but also explain what properties of Semantic-Web software made developers come up with OTM. Understanding the latter will be essential to get nonexpert software developers to use Semantic-Web technologies in their software. KW - Resource description framework KW - Software KW - Java KW - Data models KW - Programming KW - Interviews Y1 - 2012 U6 - https://doi.org/10.1109/TSMCC.2011.2151282 SN - 1094-6977 VL - 42 IS - 1 SP - 15 EP - 24 PB - Inst. of Electr. and Electronics Engineers CY - Piscataway ER - TY - JOUR A1 - de Vera, Jean-Pierre Paul A1 - Böttger, Ute A1 - de la Torre Nötzel, Rosa A1 - Sanchez, Francisco J. A1 - Grunow, Dana A1 - Schmitz, Nicole A1 - Lange, Caroline A1 - Hübers, Heinz-Wilhelm A1 - Billi, Daniela A1 - Baque, Mickael A1 - Rettberg, Petra A1 - Rabbow, Elke A1 - Reitz, Günther A1 - Berger, Thomas A1 - Möller, Ralf A1 - Bohmeier, Maria A1 - Horneck, Gerda A1 - Westall, Frances A1 - Jänchen, Jochen A1 - Fritz, Jörg A1 - Meyer, Cornelia A1 - Onofri, Silvano A1 - Selbmann, Laura A1 - Zucconi, Laura A1 - Kozyrovska, Natalia A1 - Leya, Thomas A1 - Foing, Bernard A1 - Demets, Rene A1 - Cockell, Charles S. A1 - Bryce, Casey A1 - Wagner, Dirk A1 - Serrano, Paloma A1 - Edwards, Howell G. M. A1 - Joshi, Jasmin Radha A1 - Huwe, Björn A1 - Ehrenfreund, Pascale A1 - Elsaesser, Andreas A1 - Ott, Sieglinde A1 - Meessen, Joachim A1 - Feyh, Nina A1 - Szewzyk, Ulrich A1 - Jaumann, Ralf A1 - Spohn, Tilman T1 - Supporting Mars exploration BIOMEX in Low Earth Orbit and further astrobiological studies on the Moon using Raman and PanCam technology JF - Planetary and space science N2 - The Low Earth Orbit (LEO) experiment Biology and Mars Experiment (BIOMEX) is an interdisciplinary and international space research project selected by ESA. The experiment will be accommodated on the space exposure facility EXPOSE-R2 on the International Space Station (ISS) and is foreseen to be launched in 2013. The prime objective of BIOMEX is to measure to what extent biomolecules, such as pigments and cellular components, are resistant to and able to maintain their stability under space and Mars-like conditions. The results of BIOMEX will be relevant for space proven biosignature definition and for building a biosignature data base (e.g. the proposed creation of an international Raman library). The library will be highly relevant for future space missions such as the search for life on Mars. The secondary scientific objective is to analyze to what extent terrestrial extremophiles are able to survive in space and to determine which interactions between biological samples and selected minerals (including terrestrial, Moon- and Mars analogs) can be observed under space and Mars-like conditions. In this context, the Moon will be an additional platform for performing similar experiments with negligible magnetic shielding and higher solar and galactic irradiation compared to LEO. Using the Moon as an additional astrobiological exposure platform to complement ongoing astrobiological LEO investigations could thus enhance the chances of detecting organic traces of life on Mars. We present a lunar lander mission with two related objectives: a lunar lander equipped with Raman and PanCam instruments which can analyze the lunar surface and survey an astrobiological exposure platform. This dual use of testing mission technology together with geo- and astrobiological analyses will significantly increase the science return, and support the human preparation objectives. It will provide knowledge about the Moon's surface itself and, in addition, monitor the stability of life-markers, such as cells, cell components and pigments, in an extraterrestrial environment with much closer radiation properties to the surface of Mars. The combination of a Raman data base of these data together with data from LEO and space simulation experiments, will lead to further progress on the analysis and interpretation of data that we will obtain from future Moon and Mars exploration missions. KW - Moon KW - Mars KW - Low Earth Orbit KW - Astrobiology KW - Instrumentation KW - Spectroscopy KW - Biosignature Y1 - 2012 U6 - https://doi.org/10.1016/j.pss.2012.06.010 SN - 0032-0633 VL - 74 IS - 1 SP - 103 EP - 110 PB - Elsevier CY - Oxford ER - TY - JOUR A1 - Ohuchi, Tomohiro A1 - Nishihara, Yu A1 - Kawazoe, Takaaki A1 - Spengler, Dirk A1 - Shiraishi, Rei A1 - Suzuki, Akio A1 - Kikegawa, Takumi A1 - Ohtani, Eiji T1 - Superplasticity in hydrous melt-bearing dunite Implications for shear localization in Earth's upper mantle JF - Earth & planetary science letters N2 - Deformation experiments on hydrous melt-bearing dunite (olivine+4 vol% orthopyroxene+4 vol% clinopyroxene with less than 2.5 vol% of the melt phase) were conducted at pressures of 1.3-5.7 GPa and temperatures of 1270-1490 K in order to explore the effect of intergranular fluids on the plastic flow of olivine in Earth's upper mantle. The strain rate was proportional to steady-state creep strength to the 2.1 power, and the creep strength markedly increased with increase in grain size. Developments of the crystallographic preferred orientation of olivine and flattening of olivine grains were hardly observed even after 33-55% shortening of the samples. These observations show that grain boundary sliding (GBS) dominated the deformation of olivine (i.e., superplasticity). The creep strength of hydrous melt-bearing dunite was 2-5 times lower than that of melt-free dunite. The dependence of creep rate on melt fraction is known to be expressed empirically as (epsilon) over dot(phi) = (epsilon) over dot(0) exp(alpha phi), where alpha is a constant and phi is the melt fraction. The experimentally obtained value of alpha was in the range of 150-230, corresponding to 5-7 times the reported values for the olivine-basalt system at 0.3 GPa (i.e., creep strength of dunite was efficiently reduced by the hydrous melt). Superplasticity is the dominant creep mechanism of olivine in fluid-bearing fine-grained peridotites under low-temperature and high-stress conditions (i.e., peridotite shear zones in the upper mantle). Superplasticity induced by geological fluids would play an important role in the shear localization (and thus initiation of subduction) in the upper mantle. KW - olivine KW - hydrous melt KW - grain boundary sliding KW - superplasticity KW - shear localization KW - subduction Y1 - 2012 U6 - https://doi.org/10.1016/j.epsl.2012.04.032 SN - 0012-821X VL - 335 IS - 12 SP - 59 EP - 71 PB - Elsevier CY - Amsterdam ER - TY - JOUR A1 - Böniger, Urs A1 - Tronicke, Jens T1 - Subsurface utility extraction and characterization combining GPR symmetry and polarization attributes JF - IEEE transactions on geoscience and remote sensing N2 - Polarization of the electromagnetic wavefield has significant implications for the acquisition and interpretation of ground-penetrating radar (GPR) data. Based on the geometrical and physical properties of the subsurface scatterer and the physical properties of its surrounding material, strong polarization phenomena might occur. Here, we develop an attribute-based analysis approach to extract and characterize buried utility pipes using two broadside antenna configurations. First, we enhance and extract the utilities by making use of their distinct symmetric nature through the application of a symmetry-enhancing image-processing algorithm known as phase symmetry. Second, we assess the polarization characteristics by calculating two attributes (polarization angle and linearity) using principal component analysis. Combination of attributes derived from these steps into a novel depolarization attribute allows one to efficiently detect and distinguish different utilities present within 3-D GPR data. The performance of our analysis approach is illustrated using synthetic examples and evaluated using field examples (including a dual-configuration 3-D data set) collected across a field site, where detailed ground-truth information is available. Our results demonstrate that the proposed approach allows for a more detailed extraction and combination of utility relevant information compared to approaches relying on single-component data and, thus, eases the interpretation of multicomponent GPR data sets. KW - Multicomponent ground-penetrating radar (GPR) data KW - phase symmetry KW - pipe detection KW - polarization analysis KW - principal component analysis (PCA) Y1 - 2012 U6 - https://doi.org/10.1109/TGRS.2011.2163413 SN - 0196-2892 SN - 1558-0644 VL - 50 IS - 3 SP - 736 EP - 746 PB - Inst. of Electr. and Electronics Engineers CY - Piscataway ER - TY - GEN A1 - Rothweiler, Monika A1 - Chilla, Solveig A1 - Clahsen, Harald T1 - Subject−verb agreement in Specific Language Impairment BT - a study of monolingual and bilingual German-speaking children T2 - Postprints der Universität Potsdam Humanwissenschaftliche Reihe N2 - This study investigates phenomena that have been claimed to be indicative of Specific Language Impairment (SLI) in German, focusing on subject-verb agreement marking. Longitudinal data from fourteen German-speaking children with SLI, seven monolingual and seven Turkish-German successive bilingual children, were examined. We found similar patterns of impairment in the two participant groups. Both the monolingual and the bilingual children with SLI had correct (present vs. preterit) tense marking and produced syntactically complex sentences such as embedded clauses and wh-questions, but were limited in reliably producing correct agreement-marked verb forms. These contrasts indicate that agreement marking is impaired in German-speaking children with SLI, without any necessary concurrent deficits in either the CP-domain or in tense marking. Our results also show that it is possible to identify SLI from an early successive bilingual child's performance in one of her two languages. T3 - Zweitveröffentlichungen der Universität Potsdam : Humanwissenschaftliche Reihe - 510 KW - verb morphology KW - tense deficit KW - agreement deficit KW - Turkish−German SLI Y1 - 2019 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-415122 SN - 1866-8364 IS - 510 ER -