@phdthesis{Garcia2018,
  author    = {Garcia, Rowena},
  title     = {Thematic role assignment and word order preferences in the child language acquisition of Tagalog},
  address   = {Potsdam},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-421742},
  school      = {Universit{\"a}t Potsdam},
  pages     = {xvii, 201},
  year      = {2018},
  abstract  = {A critical task in daily communications is identifying who did what to whom in an utterance, or assigning the thematic roles agent and patient in a sentence. This dissertation is concerned with Tagalog-speaking children's use of word order and morphosyntactic markers for thematic role assignment. It aims to explain children's difficulties in interpreting sentences with a non-canonical order of arguments (i.e., patient-before-agent) by testing the predictions of the following accounts: the frequency account (Demuth, 1989), the Competition model (MacWhinney \& Bates, 1989), and the incremental processing account (Trueswell \& Gleitman, 2004). Moreover, the experiments in this dissertation test the influence of a word order strategy in a language like Tagalog, where the thematic roles are always unambiguous in a sentence, due to its verb-initial order and its voice-marking system. In Tagalog's voice-marking system, the inflection on the verb indicates the thematic role of the noun marked by 'ang.' First, the possible basis for a word order strategy in Tagalog was established using a sentence completion experiment given to adults and 5- and 7-year-old children (Chapter 2) and a child-directed speech corpus analysis (Chapter 3). In general, adults and children showed an agent-before-patient preference, although adults' preference was also affected by sentence voice. Children's comprehension was then examined through a self-paced listening and picture verification task (Chapter 3) and an eye-tracking and picture selection task (Chapter 4), where word order (agent-initial or patient-initial) and voice (agent voice or patient voice) were manipulated. Offline (i.e., accuracy) and online (i.e., listening times, looks to the target) measures revealed that 5- and 7-year-old Tagalog-speaking children had a bias to interpret the first noun as the agent. Additionally, the use of word order and morphosyntactic markers was found to be modulated by voice. In the agent voice, children relied more on a word order strategy; while in the patient voice, they relied on the morphosyntactic markers. These results are only partially explained by the accounts being tested in this dissertation. Instead, the findings support computational accounts of incremental word prediction and learning such as Chang, Dell, \& Bock's (2006) model.},
  language  = {en}
}
@phdthesis{Paganini2018,
  author    = {Paganini, Claudio Francesco},
  title     = {The role of trapping in black hole spacetimes},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-414686},
  school      = {Universit{\"a}t Potsdam},
  pages     = {v, 138},
  year      = {2018},
  abstract  = {In the here presented work we discuss a series of results that are all in one way or another connected to the phenomenon of trapping in black hole spacetimes. First we present a comprehensive review of the Kerr-Newman-Taub-NUT-de-Sitter family of black hole spacetimes and their most important properties. From there we go into a detailed analysis of the bahaviour of null geodesics in the exterior region of a sub-extremal Kerr spacetime. We show that most well known fundamental properties of null geodesics can be represented in one plot. In particular, one can see immediately that the ergoregion and trapping are separated in phase space. We then consider the sets of future/past trapped null geodesics in the exterior region of a sub-extremal Kerr-Newman-Taub-NUT spacetime. We show that from the point of view of any timelike observer outside of such a black hole, trapping can be understood as two smooth sets of spacelike directions on the celestial sphere of the observer. Therefore the topological structure of the trapped set on the celestial sphere of any observer is identical to that in Schwarzschild. We discuss how this is relevant to the black hole stability problem. In a further development of these observations we introduce the notion of what it means for the shadow of two observers to be degenerate. We show that, away from the axis of symmetry, no continuous degeneration exists between the shadows of observers at any point in the exterior region of any Kerr-Newman black hole spacetime of unit mass. Therefore, except possibly for discrete changes, an observer can, by measuring the black holes shadow, determine the angular momentum and the charge of the black hole under observation, as well as the observer's radial position and angle of elevation above the equatorial plane. Furthermore, his/her relative velocity compared to a standard observer can also be measured. On the other hand, the black hole shadow does not allow for a full parameter resolution in the case of a Kerr-Newman-Taub-NUT black hole, as a continuous degeneration relating specific angular momentum, electric charge, NUT charge and elevation angle exists in this case. We then use the celestial sphere to show that trapping is a generic feature of any black hole spacetime. In the last chapter we then prove a generalization of the mode stability result of Whiting (1989) for the Teukolsky equation for the case of real frequencies. The main result of the last chapter states that a separated solution of the Teukolsky equation governing massless test fields on the Kerr spacetime, which is purely outgoing at infinity, and purely ingoing at the horizon, must vanish. This has the consequence, that for real frequencies, there are linearly independent fundamental solutions of the radial Teukolsky equation which are purely ingoing at the horizon, and purely outgoing at infinity, respectively. This fact yields a representation formula for solutions of the inhomogenous Teukolsky equation, and was recently used by Shlapentokh-Rothman (2015) for the scalar wave equation.},
  language  = {en}
}
@phdthesis{Jovanovic2018,
  author    = {Jovanovic, Nenad},
  title     = {The comprehension of the passive voice by different populations and the effects of structural priming on this process},
  doi       = {10.25932/publishup-47590},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-475900},
  school      = {Universit{\"a}t Potsdam},
  pages     = {viii, 164},
  year      = {2018},
  abstract  = {This thesis investigates the comprehension of the passive voice in three distinct populations. First, the comprehension of passives by adult German speakers was studied, followed by an examination of how German-speaking children comprehend the structure. Finally, bilingual Mandarin-English speakers were tested on their comprehension of the passive voice in English, which is their L2. An integral part of testing the comprehension in all three populations is the use of structural priming. In each of the three distinct parts of the research, structural priming was used for a specific reason. In the study involving adult German speakers, productive and receptive structural priming was directly compared. The goal was to see the effect the two priming modalities have on language comprehension. In the study on German-acquiring children, structural priming was an important tool in answering the question regarding the delayed acquisition of the passive voice. Finally, in the study on the bilingual population, cross-linguistic priming was used to investigate the importance of word order in the priming effect, since Mandarin and English have different word orders in passive voice sentences.},
  language  = {en}
}
@phdthesis{Biewener2018,
  author    = {Biewener, Ann-Kathrin},
  title     = {S{\"a}kularisierung im Heiligen Land?},
  doi       = {10.25932/publishup-42491},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-424916},
  school      = {Universit{\"a}t Potsdam},
  pages     = {241},
  year      = {2018},
  abstract  = {Von einer S{\"a}kularisierung in einem Land wie Israel zu sprechen, wo die Religion offensichtlich einen wichtigen Teil des {\"o}ffentlichen Lebens darstellt, scheint widerspr{\"u}chlich zu sein. Doch Israel befindet sich bedingt durch Globalisierung, Pluralisierung und Modernisierung an einem Scheideweg. Teile der israelischen Gesellschaft s{\"a}kularisieren sich bereits. Die religi{\"o}se orthodoxe Vorherrschaft scheint zu br{\"o}ckeln. Kann jedoch deswegen von einem Mentalit{\"a}tswandel oder einer S{\"a}kularisierung des Staates gesprochen werden? Kann ein S{\"a}kularisierungsprozess in Israel erfolgreich sein? Wie muss ein s{\"a}kularer Staat beschaffen sein, um den unterschiedlichen religi{\"o}sen Denominationen die gleichen M{\"o}glichkeiten zu bieten? Welche Rolle spielen dabei die j{\"u}dische Diaspora, Einwanderungen und gesellschaftliche Minderheiten? Ziel der vorliegenden Arbeit ist es diese Fragen zu er{\"o}rtern. Auch wenn die enge Verkn{\"u}pfung von Nation und Religion im Judentum eine S{\"a}kularisierung scheinbar unm{\"o}glich macht, so erlaubt unter Bezugnahme der Konzepte von S{\"a}kularismus und Nationalismus im Kontext der historischen Entwicklungen des Judentums eine differenziertere Betrachtung dieser Verkn{\"u}pfung. Durch die Nutzung von unterschiedlichen qualitativen Methoden, wie der hermeneutischen Methode zur Betrachtung der verschiedenen theoretischen Begriffe und der Analyse des Verh{\"a}ltnisses von Nation und Religion im Judentum; der Nutzung von Zeitungsartikel zur Aufarbeitung der aktuellen Debatten in der israelischen Gesellschaft; der Auswertung von Statistiken; sowie der Durchf{\"u}hrung von Experteninterviews erlauben einen vielseitigen Zugang zum Forschungsgegenstand. Letztendlich soll aufgezeigt werden, dass sich Israel zwar zunehmend s{\"a}kularisiert, aber vor verschiedenen Herausforderungen, wie dem gesellschaftlichen Pluralismus, der instabilen Sicherheitslage, sowie einem zunehmenden religi{\"o}sen Nationalismus steht.},
  language  = {de}
}
@phdthesis{Tan2018,
  author    = {Tan, Li},
  title     = {Synthesis, assembly and thermo-responsivity of polymer-functionalized magnetic cobalt nanoparticles},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-418153},
  school      = {Universit{\"a}t Potsdam},
  pages     = {X, 111},
  year      = {2018},
  abstract  = {This thesis mainly covers the synthesis, surface modification, magnetic-field-induced assembly and thermo-responsive functionalization of superparamagnetic Co NPs initially stabilized by hydrophobic small molecules oleic acid (OA) and trioctylphosphine oxide (TOPO), as well as the synthesis of both superparamagnetic and ferromagnetic Co NPs by using end-functionalized-polystyrene as stabilizer. Co NPs, due to their excellent magnetic and catalytic properties, have great potential application in various fields, such as ferrofluids, catalysis, and magnetic resonance imaging (MRI). Superparamagnetic Co NPs are especially interesting, since they exhibit zero coercivity. They get magnetized in an external magnetic field and reach their saturation magnetization rapidly, but no magnetic moment remains after removal of the applied magnetic field. Therefore, they do not agglomerate in the body when they are used in biomedical applications. Normally, decomposition of metallic precursors at high temperature is one of the most important methods in preparation of monodisperse magnetic NPs, providing tunability in size and shape. Hydrophobic ligands like OA, TOPO and oleylamine are often used to both control the growth of NPs and protect them from agglomeration. The as-prepared magnetic NPs can be used in biological applications as long as they are transferred into water. Moreover, their supercrystal assemblies have the potential for high density data storage and electronic devices. In addition to small molecules, polymers can also be used as surfactants for the synthesis of ferromagnetic and superparamagnetic NPs by changing the reaction conditions. Therefore, chapter 2 gives an overview on the basic concept of synthesis, surface modification and self-assembly of magnetic nanoparticles. Various examples were used to illustrate the recent work. The hydrophobic Co NPs synthesized with small molecules as surfactants limit their biological applications, which require a hydrophilic or aqueous environment. Surface modification (e.g., ligand exchange) is a general idea for either phase transition or surface-functionalization. Therefore, in chapter 3, a ligand exchange process was conducted to functionalize the surface of Co NPs. PNIPAM is one of the most popular smart polymers and its lower critical solution temperature (LCST) is around 32 °C, with a reversible change in the conformation structure between hydrophobic and hydrophilic. The novel nanocomposites of superparamagnetic Co NPs and thermo-responsive PNIPAM are of great interest. Thus, well-defined superparamagnetic Co NPs were firstly synthesized through the thermolysis of cobalt carbonyl by using OA and TOPO as surfactants. A functional ATRP initiator, containing an amine (as anchoring group) and a 2-bromopropionate group (SI-ATRP initiator), was used to replace the original ligands. This process is rapid and facial for efficient surface functionalization and afterwards the Co NPs can be dispersed into polar solvent DMF without aggregation. FT-IR spectroscopy showed that the TOPO was completely replaced, but a small amount of OA remained on the surface. A TGA measurement allowed the calculation of the grafting density of the initiator as around 3.2 initiator/nm2. Then, the surface-initiated ATRP was conducted for the polymerization of NIPAM on the surface of Co NPs and rendered the nanocomposites water-dispersible. A temperature-dependent dynamic light scattering study showed the aggregation behavior of PNIPAM-coated Co NPs upon heating and this process was proven to be reversible. The combination of superparamagnetic and thermo-responsive properties in these hybrid nanoparticles is promising for future applications e.g. in biomedicine. In chapter 4, the magnetic-field-induced assembly of superparamagnetic cobalt nanoparticles both on solid substrates and at liquid-air interface was investigated. OA- and TOPO-coated Co NPs were synthesized via the thermolysis of cobalt carbonyl and dispersed into either hexane or toluene. The Co NP dispersion was dropped onto substrates (e.g., TEM grid, silicon wafer) and at liquid-air (water-air or ethylene glycol-air) interface. Due to the attractive dipolar interaction, 1-D chains formed in the presence of an external magnetic field. It is known that the concentration and the strength of the magnetic field can affect the assembly behavior of superparamagnetic Co NPs. Therefore, the influence of these two parameters on the morphology of the assemblies was studied. The formed 1-D chains were shorter and flexible at either lower concentration of the Co NP dispersion or lower strength of the external magnetic field due to thermal fluctuation. However, by increasing either the concentration of the NP dispersion or the strength of the applied magnetic field, these chains became longer, thicker and straighter. The reason could be that a high concentration led to a high fraction of short dipolar chains, and their interaction resulted in longer and thicker chains under applied magnetic field. On the other hand, when the magnetic field increased, the induced moments of the magnetic nanoparticles became larger, which dominated over the thermal fluctuation. Thus, the formed short chains connected to each other and grew in length. Thicker chains were also observed through chain-chain interaction. Furthermore, the induced moments of the NPs tended to direct into one direction with increased magnetic field, thus the chains were straighter. In comparison between the assembly on substrates, at water-air interface and at ethylene glycol-air interface, the assembly of Co NPs in hexane dispersion at ethylene glycol-air interface showed the most regular and homogeneous chain structures due to the better spreading of the dispersion on ethylene glycol subphase than on water subphase and substrates. The magnetic-field-induced assembly of superparamagnetic nanoparticles could provide a powerful approach for applications in data storage and electronic devices. Chapter 5 presented the synthesis of superparamagnetic and ferromagnetic cobalt nanoparticles through a dual-stage thermolysis of cobalt carbonyl (Co2(CO)8) by using polystyrene as surfactant. The amine end-functionalized polystyrene surfactants with different molecular weight were prepared via atom transfer radical polymerization technique. The molecular weight determination of polystyrene was conducted by gel permeation chromatography (GPC) and matrix-assisted laser desorption/ionization time-of-flight (MALDI-ToF) mass spectrometry techniques. The results showed that, when the molecular weight distribution is low (Mw/Mn < 1.2), the measurement by GPC and MALDI-ToF MS provided nearly similar results. For example, the molecular weight of 10600 Da was obtained by MALDI-ToF MS, while GPC gave 10500 g/mol (Mw/Mn = 1.17). However, if the polymer is poly distributed, MALDI-ToF MS cannot provide an accurate value. This was exemplified for a polymer with a molecular weight of 3130 Da measured by MALDI-TOF MS, while GPC showed 2300 g/mol (Mw/Mn = 1.38). The size, size distribution and magnetic properties of the hybrid particles were different by changing either the molecular weight or concentration of the polymer surfactants. The analysis from TEM characterization showed that the size of cobalt nanoparticles stabilized with polystyrene of lower molecular weight (Mn = 2300 g/mol) varied from 12-22 nm, while the size with middle (Mn = 4500 g/mol) and higher molecular weight (Mn = 10500 g/mol) of polystyrene-coated cobalt nanoparticles showed little change. Magnetic measurements exhibited that the small cobalt particles (12 nm) were superparamagnetic, while larger particles (21 nm) were ferromagnetic and assembled into 1-D chains. The grafting density calculated from thermogravimetric analysis showed that a higher grafting density of polystyrene was obtained with lower molecular weight (Mn = 2300 g/mol) than those with higher molecular weight (Mn = 10500 g/mol). Due to the larger steric hindrance, polystyrene with higher molecular weight cannot form a dense shell on the surface of the nanoparticles, which resulted in a lower grafting density. Wide angle X-ray scattering measurements revealed the epsilon cobalt crystalline phases of both superparamagnetic Co NPs coated with polystyrene (Mn = 2300 g/mol) and ferromagnetic Co NPs coated with polystyrene (Mn = 10500 g/mol). Furthermore, a stability study showed that PS-Co NPs prepared with higher polymer concentration and polymer molecular weight exhibited a better stability.},
  language  = {en}
}
@phdthesis{Karras2018,
  author    = {Karras, Manfred},
  title     = {Synthesis of enantiomerically pure helical aromatics such as NHC ligands and their use in asymmetric catalysis},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-421497},
  school      = {Universit{\"a}t Potsdam},
  pages     = {121},
  year      = {2018},
  abstract  = {Diese Arbeit besch{\"a}ftigt sich mit der enantiomerenreinen Synthese helikaler, aromatischer Verbindungen. Verschiedene Verbindungen dieses Typs wurden erfolgreich hergestellt und charakterisiert. Desweiteren wurden einige der neuen Verbindungen in {\"U}bergangsmetallkomplexe eingebaut und diese dann als Katalysatoren f{\"u}r Metathese und Kreuzkupplungen getestet. Einer der getesteten Katalysatoren zeigte vielversprechende Ergebnisse in der asymmetrischen Olefinmetathese. Die Struktur des neuen Katalysators wurde untersucht. Anhand der Struktur des neuen Katalysators wurden R{\"u}ckschl{\"u}sse auf einen m{\"o}glichen Mechanismus gezogen.},
  language  = {en}
}
@phdthesis{Dai2018,
  author    = {Dai, Xiaolin},
  title     = {Synthesis of artificial building blocks for sortase-mediated ligation and their enzymatic linkage},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-420060},
  school      = {Universit{\"a}t Potsdam},
  pages     = {XIV, 125},
  year      = {2018},
  abstract  = {Das Enzym Sortase A katalysiert die Bildung einer Peptidbindung zwischen der Erkennungssequenz LPXTG und einem Oligoglycin. W{\"a}hrend vielf{\"a}ltige Ligationen zwischen Proteinen und verschiedenen Biomolek{\"u}len, Proteinen und kleinen synthetischen Molek{\"u}len, sowie Proteinen und Oberfl{\"a}chen durchgef{\"u}hrt wurden, besteht das Ziel dieser Arbeit darin, die Sortase-katalysierte Verlinkung von synthetischen Bausteinen zu untersuchen. Dies k{\"o}nnte den Weg bereiten f{\"u}r die Anwendung von Sortase A f{\"u}r chemische Aufgabenstellungen und eventuell sogar in den Materialwissenschaften. F{\"u}r diese grunds{\"a}tzliche Untersuchung wurden die verwendeten Bausteine zun{\"a}chst so einfach wie m{\"o}glich gehalten und leicht zug{\"a}ngliche SiO2 Nanopartikel und kommerziell erh{\"a}ltliche Polymerbl{\"o}cke ausgew{\"a}hlt. Die Bausteine wurden als erstes mit den Peptidsequenzen f{\"u}r Sortase-vermittelte Ligationen funktionalisiert. SiO2 Nanopartikel wurden mit Durchmessern von 60 und 200 nm hergestellt und mit C=C Doppelbindungen oberfl{\"a}chenmodifiziert. Dann wurden Peptide mit einem terminalen Cystein kovalent durch eine Thiol-en Reaktion angebunden. An die 60 nm NP wurden Peptide mit einem Pentaglycin und an die 200 nm Partikel Peptide mit LPETG Sequenz gebunden. Auf die gleiche Art und Weise wurden Peptide mit terminalem Cystein an die Polymere Polyethylenglykol (PEG) und Poly(N Isopropylacrylamid) (PNIPAM), die beide {\"u}ber C=C Endgruppen verf{\"u}gen, gebunden und G5-PEG und PNIPAM-LPETG Konjugate erhalten. Mit den vier Bausteinen wurden nun durch Sortase-vermittelte Ligation NP-Polymer Hybride, NP-NP und Polymer-Polymer Strukturen hergestellt und die Produkte u. a. durch Transmissionselektronen-mikroskopie, MALDI-ToF Massenspektrometrie sowie Dynamische Lichtstreuung charakterisiert. Die Verlinkung dieser synthetischen Bausteine konnte eindeutig gezeigt werden. Das Verwenden von kommerziell erh{\"a}ltlichen Polymeren hat jedoch zu einem Gemisch der Polymer-Peptid Konjugate mit unmodifiziertem Polymer gef{\"u}hrt, welches nicht gereinigt werden konnte. Deswegen wurden anschließend Synthesestrategien f{\"u}r reine Peptid-Polymer und Polymer-Peptid Konjugate als Bausteine f{\"u}r Sortase-vermittelte Ligationen entwickelt. Diese basieren auf der RAFT Polymerisation mit CTAs, die entweder an N- oder C-Terminus eines Peptids gebunden sind. GG-PNIPAM wurde durch das Anbinden eines geeigneten RAFT CTAs an Fmoc-GG in einer Veresterungsreaktion, Polymerisation von NIPAM und Abspalten der Fmoc Schutzgruppe synthetisiert. Weiterhin wurden mehrere Peptide durch Festphasen-Peptidsynthese erhalten. Die Anbindung eines RAFT CTAs (oder eines Polymerisationsinitiators) an den N-Terminus eines Peptids kann automatisiert als letzter Schritt in einem Peptid-Synthetisierer erfolgen. Die Synthese eines solchen Konjugats konnte in dem Zeithorizont dieser Arbeit noch nicht erreicht werden. Jedoch existieren mehrere vielversprechende Strategien, um diesen Ansatz mit verschiedenen Kopplungsreagenzien zur Anbindung des CTAs fortzusetzen. Solche Polymer Bausteine k{\"o}nnen in Zukunft f{\"u}r die Synthese von Protein-Polymer Konjugaten durch Sortase-Katalyse verwendet werden. Außerdem kann der Ansatz auch f{\"u}r die Synthese von Block-Copolymeren aus Polymerbl{\"o}cken mit Peptidmotiven an beiden Enden ausgebaut werden. Auch wenn bei der grunds{\"a}tzlichen Untersuchung im Rahmen dieser Arbeit Hybridstrukturen hergestellt wurden, die auch durch traditionelle chemische Synthesen erhalten werden k{\"o}nnten, wird ein Bausatz solcher Bausteine in Zukunft die Synthese neuer Materialien erm{\"o}glichen und kann auch den Weg f{\"u}r die Anwendung von Enzymen in den Materialwissenschaften ebnen. In Erg{\"a}nzung zu Nanopartikeln und Block-Copolymeren k{\"o}nnen dann auch Hybridmaterialien unter Einbezug von Protein-basierten Bausteinen hergestellt werden. Daher k{\"o}nnten Sortase Enzyme zu einem Werkzeug werden, welches etablierte chemische Verlinkungstechniken erg{\"a}nzt und mit den hoch spezifischen Peptidmotiven {\"u}ber funktionale Einheiten verf{\"u}gt, die orthogonal zu allen chemischen Gruppen sind.},
  language  = {en}
}
@phdthesis{Quade2018,
  author    = {Quade, Markus},
  title     = {Symbolic regression for identification, prediction, and control of dynamical systems},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-419790},
  school      = {Universit{\"a}t Potsdam},
  pages     = {xiii, 134},
  year      = {2018},
  abstract  = {In the present work, we use symbolic regression for automated modeling of dynamical systems. Symbolic regression is a powerful and general method suitable for data-driven identification of mathematical expressions. In particular, the structure and parameters of those expressions are identified simultaneously. We consider two main variants of symbolic regression: sparse regression-based and genetic programming-based symbolic regression. Both are applied to identification, prediction and control of dynamical systems. We introduce a new methodology for the data-driven identification of nonlinear dynamics for systems undergoing abrupt changes. Building on a sparse regression algorithm derived earlier, the model after the change is defined as a minimum update with respect to a reference model of the system identified prior to the change. The technique is successfully exemplified on the chaotic Lorenz system and the van der Pol oscillator. Issues such as computational complexity, robustness against noise and requirements with respect to data volume are investigated. We show how symbolic regression can be used for time series prediction. Again, issues such as robustness against noise and convergence rate are investigated us- ing the harmonic oscillator as a toy problem. In combination with embedding, we demonstrate the prediction of a propagating front in coupled FitzHugh-Nagumo oscillators. Additionally, we show how we can enhance numerical weather predictions to commercially forecast power production of green energy power plants. We employ symbolic regression for synchronization control in coupled van der Pol oscillators. Different coupling topologies are investigated. We address issues such as plausibility and stability of the control laws found. The toolkit has been made open source and is used in turbulence control applications. Genetic programming based symbolic regression is very versatile and can be adapted to many optimization problems. The heuristic-based algorithm allows for cost efficient optimization of complex tasks. We emphasize the ability of symbolic regression to yield white-box models. In contrast to black-box models, such models are accessible and interpretable which allows the usage of established tool chains.},
  language  = {en}
}
@phdthesis{ChaleawlertUmpon2018,
  author    = {Chaleawlert-Umpon, Saowaluk},
  title     = {Sustainable electrode materials based on lignin},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-411793},
  school      = {Universit{\"a}t Potsdam},
  pages     = {114},
  year      = {2018},
  abstract  = {The utilization of lignin as renewable electrode material for electrochemical energy storage is a sustainable approach for future batteries and supercapacitors. The composite electrode was fabricated from Kraft lignin and conductive carbon and the charge storage contribution was determined in terms of electrical double layer (EDL) and redox reactions. The important factors at play for achieving high faradaic charge storage capacity contribute to high surface area, accessibility of redox sites in lignin and their interaction with conductive additives. A thinner layer of lignin covering the high surface area of carbon facilitates the electron transfer process with a shorter pathway from the active sites of nonconductive lignin to the current collector leading to the improvement of faradaic charge storage capacity. Composite electrodes from lignin and carbon would be even more sustainable if the fluorinated binder can be omitted. A new route to fabricate a binder-free composite electrode from Kraft lignin and high surface area carbon has been proposed by crosslinking lignin with glyoxal. A high molecular weight of lignin is obtained to enhance both electroactivity and binder capability in composite electrodes. The order of the processing step of crosslinking lignin on the composite electrode plays a crucial role in achieving a stable electrode and high charge storage capacity. The crosslinked lignin based electrodes are promising since they allow for more stable, sustainable, halogen-free and environmentally benign devices for energy storage applications. Furthermore, improvement of the amount of redox active groups (quinone groups) in lignin is useful to enhance the capacity in lithium battery applications. Direct oxidative demethylation by cerium ammonium nitrate has been carried out under mild conditions. This proves that an increase of quinone groups is able to enhance the performance of lithium battery. Thus, lignin is a promising material and could be a good candidate for application in sustainable energy storage devices.},
  language  = {en}
}
@phdthesis{Sixtus2018,
  author    = {Sixtus, Elena},
  title     = {Subtle fingers - tangible numbers: The influence of finger counting experience on mental number representations},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-420115},
  school      = {Universit{\"a}t Potsdam},
  pages     = {vi, 138},
  year      = {2018},
  abstract  = {Numbers are omnipresent in daily life. They vary in display format and in their meaning so that it does not seem self-evident that our brains process them more or less easily and flexibly. The present thesis addresses mental number representations in general, and specifically the impact of finger counting on mental number representations. Finger postures that result from finger counting experience are one of many ways to convey numerical information. They are, however, probably the one where the numerical content becomes most tangible. By investigating the role of fingers in adults' mental number representations the four presented studies also tested the Embodied Cognition hypothesis which predicts that bodily experience (e.g., finger counting) during concept acquisition (e.g., number concepts) stays an immanent part of these concepts. The studies focussed on different aspects of finger counting experience. First, consistency and further details of spontaneously used finger configurations were investigated when participants repeatedly produced finger postures according to specific numbers (Study 1). Furthermore, finger counting postures (Study 2), different finger configurations (Study 2 and 4), finger movements (Study 3), and tactile finger perception (Study 4) were investigated regarding their capability to affect number processing. Results indicated that active production of finger counting postures and single finger movements as well as passive perception of tactile stimulation of specific fingers co-activated associated number knowledge and facilitated responses towards corresponding magnitudes and number symbols. Overall, finger counting experience was reflected in specific effects in mental number processing of adult participants. This indicates that finger counting experience is an immanent part of mental number representations. Findings are discussed in the light of a novel model. The MASC (Model of Analogue and Symbolic Codes) combines and extends two established models of number and magnitude processing. Especially a symbolic motor code is introduced as an essential part of the model. It comprises canonical finger postures (i.e., postures that are habitually used to represent numbers) and finger-number associations. The present findings indicate that finger counting functions both as a sensorimotor magnitude and as a symbolic representational format and that it thereby directly mediates between physical and symbolic size. The implications are relevant both for basic research regarding mental number representations and for pedagogic practices regarding the effectiveness of finger counting as a means to acquire a fundamental grasp of numbers.},
  language  = {en}
}