TY - GEN A1 - Schwerbel, Kristin A1 - Kamitz, Anne A1 - Jaehnert, Markus A1 - Gottmann, P. A1 - Schumacher, Fabian A1 - Kleuser, Burkhard A1 - Haltenhof, T. A1 - Heyd, F. A1 - Roden, Michael A1 - Chadt, Alexandra A1 - Al-Hasani, Hadi A1 - Jonas, W. A1 - Vogel, Heike A1 - Schürmann, Annette T1 - Two immune-related GTPases prevent from hepatic fat accumulation by inducing autophagy T2 - Diabetologia : journal of the European Association for the Study of Diabetes (EASD) Y1 - 2018 SN - 0012-186X SN - 1432-0428 VL - 61 SP - S259 EP - S259 PB - Springer CY - New York ER - TY - JOUR A1 - Sellberg, Jonas A. A1 - McQueen, Trevor A. A1 - Laksmono, Hartawan A1 - Schreck, Simon A1 - Beye, Martin A1 - DePonte, Daniel P. A1 - Kennedy, Brian A1 - Nordlund, Dennis A1 - Sierra, Raymond G. A1 - Schlesinger, Daniel A1 - Tokushima, Takashi A1 - Zhovtobriukh, Iurii A1 - Eckert, Sebastian A1 - Segtnan, Vegard H. A1 - Ogasawara, Hirohito A1 - Kubicek, Katharina A1 - Techert, Simone A1 - Bergmann, Uwe A1 - Dakovski, Georgi L. A1 - Schlotter, William F. A1 - Harada, Yoshihisa A1 - Bogan, Michael J. A1 - Wernet, Philippe A1 - Föhlisch, Alexander A1 - Pettersson, Lars G. M. A1 - Nilsson, Anders T1 - X-ray emission spectroscopy of bulk liquid water in "no-man's land" JF - The journal of chemical physics : bridges a gap between journals of physics and journals of chemistr N2 - The structure of bulk liquid water was recently probed by x-ray scattering below the temperature limit of homogeneous nucleation (T-H) of similar to 232 K [J. A. Sellberg et al., Nature 510, 381-384 (2014)]. Here, we utilize a similar approach to study the structure of bulk liquid water below T-H using oxygen K-edge x-ray emission spectroscopy (XES). Based on previous XES experiments [T. Tokushima et al., Chem. Phys. Lett. 460, 387-400 (2008)] at higher temperatures, we expected the ratio of the 1b(1)' and 1b(1)" peaks associated with the lone-pair orbital in water to change strongly upon deep supercooling as the coordination of the hydrogen (H-) bonds becomes tetrahedral. In contrast, we observed only minor changes in the lone-pair spectral region, challenging an interpretation in terms of two interconverting species. A number of alternative hypotheses to explain the results are put forward and discussed. Although the spectra can be explained by various contributions from these hypotheses, we here emphasize the interpretation that the line shape of each component changes dramatically when approaching lower temperatures, where, in particular, the peak assigned to the proposed disordered component would become more symmetrical as vibrational interference becomes more important. (C) 2015 AIP Publishing LLC. Y1 - 2015 U6 - https://doi.org/10.1063/1.4905603 SN - 0021-9606 SN - 1089-7690 VL - 142 IS - 4 PB - American Institute of Physics CY - Melville ER - TY - JOUR A1 - Schreck, Simon A1 - Beye, Martin A1 - Sellberg, Jonas A. A1 - McQueen, Trevor A1 - Laksmono, Hartawan A1 - Kennedy, Brian A1 - Eckert, Sebastian A1 - Schlesinger, Daniel A1 - Nordlund, Dennis A1 - Ogasawara, Hirohito A1 - Sierra, Raymond G. A1 - Segtnan, Vegard H. A1 - Kubicek, Katharina A1 - Schlotter, William F. A1 - Dakovski, Georgi L. A1 - Moeller, Stefan P. A1 - Bergmann, Uwe A1 - Techert, Simone A1 - Pettersson, Lars G. M. A1 - Wernet, Philippe A1 - Bogan, Michael J. A1 - Harada, Yoshihisa A1 - Nilsson, Anders A1 - Föhlisch, Alexander T1 - Reabsorption of soft x-ray emission at high x-ray free-electron laserfluences JF - Physical review letters N2 - We report on oxygen K-edge soft x-ray emission spectroscopy from a liquid water jet at the Linac Coherent Light Source. We observe significant changes in the spectral content when tuning over a wide range of incident x-ray fluences. In addition the total emission yield decreases at high fluences. These modifications result from reabsorption of x-ray emission by valence-excited molecules generated by the Auger cascade. Our observations have major implications for future x-ray emission studies at intense x-ray sources. We highlight the importance of the x-ray pulse length with respect to the core-hole lifetime. Y1 - 2014 U6 - https://doi.org/10.1103/PhysRevLett.113.153002 SN - 0031-9007 SN - 1079-7114 VL - 113 IS - 15 PB - American Physical Society CY - College Park ER - TY - JOUR A1 - Kokhanovsky, Alexander A1 - Lamare, Maxim A1 - Danne, Olaf A1 - Brockmann, Carsten A1 - Dumont, Marie A1 - Picard, Ghislain A1 - Arnaud, Laurent A1 - Favier, Vincent A1 - Jourdain, Bruno A1 - Le Meur, Emmanuel A1 - Di Mauro, Biagio A1 - Aoki, Teruo A1 - Niwano, Masashi A1 - Rozanov, Vladimir A1 - Korkin, Sergey A1 - Kipfstuhl, Sepp A1 - Freitag, Johannes A1 - Hoerhold, Maria A1 - Zuhr, Alexandra A1 - Vladimirova, Diana A1 - Faber, Anne-Katrine A1 - Steen-Larsen, Hans Christian A1 - Wahl, Sonja A1 - Andersen, Jonas K. A1 - Vandecrux, Baptiste A1 - van As, Dirk A1 - Mankoff, Kenneth D. A1 - Kern, Michael A1 - Zege, Eleonora A1 - Box, Jason E. T1 - Retrieval of Snow Properties from the Sentinel-3 Ocean and Land Colour Instrument JF - Remote sensing N2 - The Sentinel Application Platform (SNAP) architecture facilitates Earth Observation data processing. In this work, we present results from a new Snow Processor for SNAP. We also describe physical principles behind the developed snow property retrieval technique based on the analysis of Ocean and Land Colour Instrument (OLCI) onboard Sentinel-3A/B measurements over clean and polluted snow fields. Using OLCI spectral reflectance measurements in the range 400-1020 nm, we derived important snow properties such as spectral and broadband albedo, snow specific surface area, snow extent and grain size on a spatial grid of 300 m. The algorithm also incorporated cloud screening and atmospheric correction procedures over snow surfaces. We present validation results using ground measurements from Antarctica, the Greenland ice sheet and the French Alps. We find the spectral albedo retrieved with accuracy of better than 3% on average, making our retrievals sufficient for a variety of applications. Broadband albedo is retrieved with the average accuracy of about 5% over snow. Therefore, the uncertainties of satellite retrievals are close to experimental errors of ground measurements. The retrieved surface grain size shows good agreement with ground observations. Snow specific surface area observations are also consistent with our OLCI retrievals. We present snow albedo and grain size mapping over the inland ice sheet of Greenland for areas including dry snow, melted/melting snow and impurity rich bare ice. The algorithm can be applied to OLCI Sentinel-3 measurements providing an opportunity for creation of long-term snow property records essential for climate monitoring and data assimilation studies-especially in the Arctic region, where we face rapid environmental changes including reduction of snow/ice extent and, therefore, planetary albedo. KW - snow characteristics KW - optical remote sensing KW - snow grain size KW - specific surface area KW - albedo KW - Sentinel 3 KW - OLCI Y1 - 2019 U6 - https://doi.org/10.3390/rs11192280 SN - 2072-4292 VL - 11 IS - 19 PB - MDPI CY - Basel ER - TY - JOUR A1 - Thulin, Mirjam A1 - Krah, Markus A1 - Meyer, Michael A. A1 - Schorsch, Ismar A1 - Brodt, Eliezer A1 - Sariel, Eliezer A1 - Yedidya, Asaf A1 - Esther, Solomon A1 - Kessler, Samuel J. A1 - Bratkin, Dimitri A1 - Sax, Benjamin E. A1 - Stair, Rose A1 - Ariel, Yaakov S. A1 - Weidner, Daniel A1 - Ebert, Sophia A1 - Martini, Annett A1 - Fischer, Bernd A1 - Thüne, Eva-Maria A1 - Bock, Dennis A1 - Engelmann, Jonas A1 - Aust, Cornelia A1 - Walter, Nancy ED - Krah, Markus ED - Thulin, Mirjam ED - Pick, Bianca T1 - PaRDeS : Zeitschrift der Vereinigung für Jüdische Studien = Cultures of Wissenschaft des Judentums at 200 T2 - PaRDeS : Zeitschrift der Vereinigung für Jüdische Studien e. V. N2 - PaRDeS, the journal of the German Association for Jewish Studies, aims at exploring the fruitful and multifarious cultures of Judaism as well as their relations to their environment within diverse areas of research. In addition, the journal promotes Jewish Studies within academic discourse and reflects on its historic and social responsibilities. N2 - PaRDeS, die Zeitschrift der Vereinigung für Jüdische Studien e. V., erforscht die fruchtbare kulturelle Vielfalt des Judentums sowie ihre Berührungspunkte zur nichtjüdischen Umwelt in unterschiedlichen Bereichen. Daneben dient die Zeitschrift als Forum zur Positionierung der Fächer Jüdische Studien und Judaistik innerhalb des wissenschaftlichen Diskurses sowie zur Diskussion ihrer historischen und gesellschaftlichen Verantwortung. T3 - PaRDeS : Zeitschrift der Vereinigung für Jüdische Studien e.V. - 24 Y1 - 2018 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-414943 SN - 978-3-86956-440-1 SN - 1614-6492 SN - 1862-7684 IS - 24 PB - Universitätsverlag Potsdam CY - Potsdam ER - TY - JOUR A1 - Jonas, Kristina A1 - Jaecks, Petra A1 - Niebuhr-Siebert, Sandra A1 - Wahl, Michael A1 - Leinweber, Juliane A1 - Bilda, Kerstin A1 - Plößel, Laura A1 - Heide, Judith A1 - Netzebandt, Jonka A1 - Brüsch, Julia A1 - Diener, Antonia A1 - Hubert, Cilly A1 - Menze, Clara A1 - Neitzel, Isabel A1 - Tenhagen, Anne A1 - Kauschke, Christina A1 - Siegmüller, Julia A1 - Sachse, Steffi A1 - Dörfler, Tobias A1 - Machleb, Franziska A1 - Seyboth, Margret A1 - Eikerling, Maren A1 - Vona, Francesco A1 - Garzotto, Franca A1 - Lorusso, Maria Luisa ED - Fritzsche, Tom ED - Breitenstein, Sarah ED - Wunderlich, Hanna ED - Ferchland, Lisa T1 - Spektrum Patholinguistik Band 14. Schwerpunktthema: Klick für Klick: Schritte in der digitalen Sprachtherapie N2 - Das 14. Herbsttreffen Patholinguistik mit dem Schwerpunktthema »Klick für Klick: Schritte in der digitalen Sprachtherapie« fand am 14.11.2020 als Online-Veranstaltung statt. Das Herbsttreffen wird seit 2007 jährlich vom Verband für Patholinguistik e.V. (vpl) in Kooperation mit dem Deutschen Bundesverband für akademische Sprachtherapie und Logopädie (dbs) und der Universität Potsdam durchgeführt. Der vorliegende Tagungsband beinhaltet die Hauptvorträge zum Schwerpunktthema sowie die Posterpräsentationen zu weiteren Themen aus der sprachtherapeutischen Forschung und Praxis. N2 - The Fourteenth Autumn Meeting Patholinguistics with its main topic »Click by click: Steps towards a digital speech/language therapy« took place online on the 14th of November 2020. This annual meeting has been organised since 2007 by the Association for Patholinguistics (vpl) in cooperation with the German Federal Association for Academic Speech/Language Therapy and Logopaedics (dbs) and the University of Potsdam. The present proceedings feature the keynote presentations on the main topic as well as articles from the poster session covering a broad range of areas in research and practice of speech/language therapy. T3 - Spektrum Patholinguistik - 14 KW - Patholinguistik KW - Sprachtherapie KW - Teletherapie KW - digitale Medien und Apps KW - Digitalisierung KW - patholinguistics KW - speech/language therapy KW - teletherapy KW - digital media and apps KW - digitalisation Y1 - 2021 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-500160 SN - 978-3-86956-507-1 SN - 1866-9433 SN - 1869-3822 IS - 14 PB - Universitätsverlag Potsdam CY - Potsdam ER - TY - JOUR A1 - Inal, Sahika A1 - Koelsch, Jonas D. A1 - Chiappisi, Leonardo A1 - Kraft, Mario A1 - Gutacker, Andrea A1 - Janietz, Dietmar A1 - Scherf, Ullrich A1 - Gradzielski, Michael A1 - Laschewsky, André A1 - Neher, Dieter T1 - Temperature-Regulated Fluorescence Characteristics of Supramolecular Assemblies Formed By a Smart Polymer and a Conjugated Polyelectrolyte JF - MACROMOLECULAR CHEMISTRY AND PHYSICS N2 - Aqueous mixtures of a coumarin-labeled non-ionic thermoresponsive copolymer and a cationic polythiophene exhibit marked changes in their fluorescence properties upon heating. At room temperature, emission from the label is significantly quenched due to energy transfer to the conjugated polyelectrolyte. Heating the mixture reduces the energy-transfer efficiency markedly, resulting in a clearly visible change of the emission color. Although the two macromolecules associate strongly at room temperature, the number of interacting sites is largely reduced upon the phase transition. Crucially, the intermolecular association does not suppress the responsiveness of the smart polymer, meaning that this concept should be applicable to chemo- or bioresponsive polymers with optical read-out, for example, as a sensor device. KW - aqueous solutions KW - conjugated polyelectrolytes KW - fluorescence (or Forster) KW - resonance energy transfer KW - phase transitions KW - thermoresponsive polymers Y1 - 2013 U6 - https://doi.org/10.1002/macp.201200493 SN - 1022-1352 VL - 214 IS - 4 SP - 435 EP - 445 PB - WILEY-V C H VERLAG GMBH CY - WEINHEIM ER - TY - JOUR A1 - Inal, Sahika A1 - Kölsch, Jonas D. A1 - Chiappisi, Leonardo A1 - Janietz, Dietmar A1 - Gradzielski, Michael A1 - Laschewsky, André A1 - Neher, Dieter T1 - Structure-related differences in the temperature-regulated fluorescence response of LCST type polymers N2 - We demonstrate new fluorophore-labelled materials based on acrylamide and on oligo(ethylene glycol) (OEG) bearing thermoresponsive polymers for sensing purposes and investigate their thermally induced solubility transitions. It is found that the emission properties of the polarity-sensitive (solvatochromic) naphthalimide derivative attached to three different thermoresponsive polymers are highly specific to the exact chemical structure of the macromolecule. While the dye emits very weakly below the LCST when incorporated into poly(N-isopropylacrylamide) (pNIPAm) or into a polyacrylate backbone bearing only short OEG side chains, it is strongly emissive in polymethacrylates with longer OEG side chains. Heating of the aqueous solutions above their cloud point provokes an abrupt increase of the fluorescence intensity of the labelled pNIPAm, whereas the emission properties of the dye are rather unaffected as OEG-based polyacrylates and methacrylates undergo phase transition. Correlated with laser light scattering studies, these findings are ascribed to the different degrees of pre-aggregation of the chains at low temperatures and to the extent of dehydration that the phase transition evokes. It is concluded that although the temperature-triggered changes in the macroscopic absorption characteristics, related to large-scale alterations of the polymer chain conformation and aggregation, are well detectable and similar for these LCST-type polymers, the micro-environment provided to the dye within each polymer network differs substantially. Considering sensing applications, this finding is of great importance since the temperature-regulated fluorescence response of the polymer depends more on the macromolecular architecture than the type of reporter fluorophore. Y1 - 2013 UR - http://pubs.rsc.org/en/content/articlepdf/2013/tc/c3tc31304b U6 - https://doi.org/10.1039/C3TC31304B ER - TY - JOUR A1 - Inal, Sahika A1 - Koelsch, Jonas D. A1 - Chiappisi, Leonardo A1 - Janietz, Dietmar A1 - Gradzielski, Michael A1 - Laschewsky, André A1 - Neher, Dieter T1 - Structure-related differences in the temperature-regulated fluorescence response of LCST type polymers JF - Journal of materials chemistry : C, Materials for optical and electronic devices N2 - We demonstrate new fluorophore-labelled materials based on acrylamide and on oligo(ethylene glycol) (OEG) bearing thermoresponsive polymers for sensing purposes and investigate their thermally induced solubility transitions. It is found that the emission properties of the polarity-sensitive (solvatochromic) naphthalimide derivative attached to three different thermoresponsive polymers are highly specific to the exact chemical structure of the macromolecule. While the dye emits very weakly below the LCST when incorporated into poly(N-isopropylacrylamide) (pNIPAm) or into a polyacrylate backbone bearing only short OEG side chains, it is strongly emissive in polymethacrylates with longer OEG side chains. Heating of the aqueous solutions above their cloud point provokes an abrupt increase of the fluorescence intensity of the labelled pNIPAm, whereas the emission properties of the dye are rather unaffected as OEG-based polyacrylates and methacrylates undergo phase transition. Correlated with laser light scattering studies, these findings are ascribed to the different degrees of pre-aggregation of the chains at low temperatures and to the extent of dehydration that the phase transition evokes. It is concluded that although the temperature-triggered changes in the macroscopic absorption characteristics, related to large-scale alterations of the polymer chain conformation and aggregation, are well detectable and similar for these LCST-type polymers, the micro-environment provided to the dye within each polymer network differs substantially. Considering sensing applications, this finding is of great importance since the temperature-regulated fluorescence response of the polymer depends more on the macromolecular architecture than the type of reporter fluorophore. Y1 - 2013 U6 - https://doi.org/10.1039/c3tc31304b SN - 2050-7526 VL - 1 IS - 40 SP - 6603 EP - 6612 PB - Royal Society of Chemistry CY - Cambridge ER - TY - GEN A1 - Inal, Sahika A1 - Kölsch, Jonas D. A1 - Chiappisi, Leonardo A1 - Janietz, Dietmar A1 - Gradzielski, Michael A1 - Laschewsky, André A1 - Neher, Dieter T1 - Structure-related differences in the temperature-regulated fluorescence response of LCST type polymers N2 - We demonstrate new fluorophore-labelled materials based on acrylamide and on oligo(ethylene glycol) (OEG) bearing thermoresponsive polymers for sensing purposes and investigate their thermally induced solubility transitions. It is found that the emission properties of the polarity-sensitive (solvatochromic) naphthalimide derivative attached to three different thermoresponsive polymers are highly specific to the exact chemical structure of the macromolecule. While the dye emits very weakly below the LCST when incorporated into poly(N-isopropylacrylamide) (pNIPAm) or into a polyacrylate backbone bearing only short OEG side chains, it is strongly emissive in polymethacrylates with longer OEG side chains. Heating of the aqueous solutions above their cloud point provokes an abrupt increase of the fluorescence intensity of the labelled pNIPAm, whereas the emission properties of the dye are rather unaffected as OEG-based polyacrylates and methacrylates undergo phase transition. Correlated with laser light scattering studies, these findings are ascribed to the different degrees of pre-aggregation of the chains at low temperatures and to the extent of dehydration that the phase transition evokes. It is concluded that although the temperature-triggered changes in the macroscopic absorption characteristics, related to large-scale alterations of the polymer chain conformation and aggregation, are well detectable and similar for these LCST-type polymers, the micro-environment provided to the dye within each polymer network differs substantially. Considering sensing applications, this finding is of great importance since the temperature-regulated fluorescence response of the polymer depends more on the macromolecular architecture than the type of reporter fluorophore. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 251 KW - anionic polymerizations KW - dilute aqueous-solutions KW - ether methacrylates KW - n-isopropylacrylamide KW - oligo(ethylene glycol) methacrylate KW - phase-transitions KW - protein interactions KW - solvatochromic fluorophore KW - thermoresponsive polymers KW - to-coil transition Y1 - 2013 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-95379 SP - 6603 EP - 6612 ER -