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This cumulative habilitation thesis presents new work on the systematics, paleoecology, and evolution of antelopes and other large mammals, focusing mainly on the late Miocene to Pleistocene terrestrial fossil record of Africa and Arabia. The studies included here range from descriptions of new species to broad-scale analyses of diversification and community evolution in large mammals over millions of years. A uniting theme is the evolution, across both temporal and spatial scales, of the environments and faunas that characterize modern African savannas today. One conclusion of this work is that macroevolutionary changes in large mammals are best characterized at regional (subcontinental to continental) and long-term temporal scales. General views of evolution developed on records that are too restricted in spatial and temporal extent are likely to ascribe too much influence to local or short-lived events. While this distinction in the scale of analysis and interpretation may seem trivial, it is challenging to implement given the geographically and temporally uneven nature of the fossil record, and the difficulties of synthesizing spatially and temporally dispersed datasets. This work attempts to do just that, bringing together primary fossil discoveries from eastern Africa to Arabia, from the Miocene to the Pleistocene, and across a wide range of (mainly large mammal) taxa. The end result is support for hypotheses stressing the impact of both climatic and biotic factors on long-term faunal change, and a more geographically integrated view of evolution in the African fossil record.
Individuals differ in their tendency to perceive injustice and in their responses towards these perceptions. Those high in justice sensitivity tend to show intense negative affective, cognitive, and behavioral responses towards injustice that in part also depend on the perspective from which injustice is perceived. The present research project showed that inter-individual differences in justice sensitivity may already be measured and observed in childhood and adolescence and that early adolescence seems an important age-range and developmental stage for the stabilization of these differences. Furthermore, the different justice sensitivity perspectives were related to different forms of externalizing (aggression, ADHD, bullying) and internalizing problem behavior (depressive symptoms) both in children and adolescents as well as in adults in cross-sectional studies. Particularly victim sensitivity may apparently constitute an important risk factor for a broad range of both externalizing and internalizing maladaptive behaviors and mental health problems as shown in those studies using longitudinal data. Regarding aggressive behavior, victim justice sensitivity may even constitute a risk factor above and beyond other important and well-established risk factors for aggression and similar sensitivity constructs that had previously been linked to this kind of behavior. In contrast, observer and perpetrator sensitivity (perpetrator sensitivity in particular) tended to show negative links with externalizing problem behavior and instead predicted prosocial behavior in children and adolescents. However, there were also detached positive relations of perpetrator sensitivity with emotional problems as well as of observer sensitivity with reactive aggression and depressive symptoms. Taken together, the findings from the present research show that justice sensitivity forms in childhood at the latest and that it may have important, long-term influences on pro- and antisocial behavior and mental health. Thus, justice sensitivity requires more attention in research on the prevention and intervention of mental health problems and antisocial behavior, such as aggression.
This habilitation thesis summarises the research work performed by the author during the last quindecennial period. The dissertation reflects his main research interests, which revolve around quantum dynamics of small-sized molecular systems, including their interactions with electromagnetic radiation or dissipative environments. This covers various dynamical processes that involve bound-bound, bound-free, and free-free molecular transitions. The latter encompass light-triggered rovibrational or rovibronic dynamics in bound molecules, molecular photodissociation induced by weak or strong laser fields, state-to-state reactive and/or inelastic molecular collisions, and phonon-driven vibrational relaxation of adsorbates at solid surfaces. Although the dissertation covers different topics of molecular reaction dynamics, most of these studies focus on nuclear quantum effects and their manifestations in experimental measures. The latter are assessed through comparison between quantum and classical predictions, and/or direct confrontation of theory and experiment. Most well known quantum concepts and effects will be encountered in this work. Yet, almost all these quantum notions find their roots in the central pillar of quantum theory, namely, the quantum superposition principle. Indeed, quantum coherence is the main source of most quantum effects, including interference, entanglement, and even tunneling. Thus, the common and predominant theme of all the investigations of this thesis is quantum coherence, and the survival or quenching of subsequent interference effects in various molecular processes. The lion's share of the dissertation is devoted to two associated quantum concepts, which are usually overlooked in computational molecular dynamics, viz. the Berry phase and identical nuclei symmetry. The importance of the latter in dynamical molecular processes and their direct fingerprints in experimental observables also rely very much on quantum coherence and entanglement. All these quantum phenomena are thoroughly discussed within the four main topics that form the core of this thesis. Each topic is described in a separate chapter, where it is briefly summarised and then illustrated with three peer-reviewed publications. The first topic deals with the relevance of quantum coherence/interference in molecular collisions, with a focus on the hydrogen-exchange reaction, H+H2 --> H2+H, and its isotopologues. For these collision processes, the significance of interference of probability amplitudes arises because of the existence of two main scattering pathways. The latter could be inelastic and reactive scattering, direct and time-delayed scattering, or two encircling reaction paths that loop in opposite senses around a conical intersection (CI) of the H3 molecular system. Our joint theoretical-experimental investigations of these processes reveal strong interference and geometric phase (GP) effects in state-to-state reaction probabilities and differential cross sections. However, these coherent effects completely cancel in integral cross sections and reaction rate constants, due to efficient dephasing of interference between the different scattering amplitudes. As byproducts of these studies, we highlight the discovery of two novel scattering mechanisms, which contradict conventional textbook pictures of molecular reaction dynamics. The second topic concerns the effect of the Berry phase on molecular photodynamics at conical intersections. To understand this effect, we developed a topological approach that separates the total molecular wavefunction of an unbound molecular system into two components, which wind in opposite senses around the conical intersection. This separation reveals that the only effect of the geometric phase is to change the sign of the relative phase of these two components. This in turn leads to a shift in the interference pattern of the molecular system---a phase shift that is reminiscient of the celebrated Aharonov-Bohm effect. This procedure is numerically illustrated with photodynamics at model standard CIs, as well as strong-field dissociation of diatomics at light-induced conical intersections (LICIs). Besides the fundamental aspect of these studies, their findings allow to interpret and predict the effect of the GP on the state-resolved or angle-resolved spectra of pump-probe experimental schemes, particularly the distributions of photofragments in molecular photodissociation experiments. The third topic pertains to the role of the indistinguishability of identical nuclei in molecular reaction dynamics, with an emphasis on dynamical localization in highly symmetric molecules. The main object of these studies is whether nuclear-spin statistics allow dynamical localization of the electronic, vibrational, or even rotational density on a specific molecular substructure or configuration rather than on another one which is identical (indistinguishable). Group-theoretic analysis of the symmetrized molecular wavefunctions of these systems shows that nuclear permutation symmetry engenders quantum entanglement between the eigenstates of the different molecular degrees of freedom. This subsequently leads to complete quenching of dynamical localization over indistinguishable molecular substructures---an observation that is in sharp contradiction with well known textbook views of iconic molecular processes. This is illustrated with various examples of quantum dynamics in symmetric double-well achiral molecules, such as the prototypical umbrella inversion motion of ammonia, electronic Kekulé dynamics in the benzene molecule, and coupled electron-nuclear dynamics in laser-induced indirect photodissociation of the dihydrogen molecular cation. The last part of the thesis is devoted to the development of approximate wavefunction approaches for phonon-induced vibrational relaxation of adsorbates (system) at surfaces (bath). Due to the so-called 'curse of dimensionality', these system-bath complexes cannot be handled with standard wavefunction methods. To alleviate the exponential scaling of the latter, we developed approximate yet quite accurate numerical schemes that have a polynomial scaling with respect to the bath dimensionality. The corresponding algorithms combine symmetry-based reductions of the full vibrational Hilbert space and iterative Krylov techniques. These approximate wavefunction approaches resemble the 'Bixon-Jortner model' and the more general 'quantum tier model'. This is illustrated with the decay of H-Si (D-Si) vibrations on a fully H(D)-covered silicon surface, which is modelled with a phonon-bath of more than two thousand oscillators. These approximate methods allow reliable estimation of the adsorbate vibrational lifetimes, and provide some insight into vibration-phonon couplings at solid surfaces. Although this topic is mainly computational, the developed wavefunction approaches permit to describe quantum entanglement between the system and bath states, and to embody some coherent effects in the time-evolution of the (sub-)system, which cannot be accounted for with the widely used 'reduced density matrix formalism'.
The direct conversion of light from the sun into usable forms of energy marks one of the central cornerstones of the change of our living from the use of fossil, non-renewable energy resources towards a more sustainable economy. Besides the necessary societal changes necessary, it is the understanding of the solids employed that is of particular importance for the success of this target. In this work, the principles and approaches of systematic-crystallographic characterisation and systematisation of solids is used and employed to allow a directed tuning of the materials properties. The thorough understanding of the solid-state forms hereby the basis, on which more applied approaches are founded.
Two material systems, which are considered as promising solar absorber materials, are at the core of this work: halide perovskites and II-IV-N2 nitride materials. While the first is renowned for its high efficiencies and rapid development in the last years, the latter is putting an emphasis on true sustainability in that toxic and scarce elements are avoided.
Und der Zukunft abgewandt
(2010)
Seit dem Ende der DDR, das den Zusammenbruch des Ostblocks und damit die Beendigung des »Kalten Kriegs« einleitete, wird verstärkt versucht, das Wesen dieses Staates zu definieren und damit seine Folgen auf wirtschaftlicher, sozialer, psychologischer und bildungspolitischer Ebene zu verstehen und einzuordnen. Alexandra Budke analysiert in diesem Band das Schulfach Geographie, das neben der Staatsbürgerkunde und der Geschichte ein zentrales Fach war und in dem die in den Lehrplänen definierte »staatsbürgerliche, weltanschauliche oder ideologische Erziehung« auf der Grundlage des Marxismus-Leninismus stattfinden sollte. Sie klärt, inwiefern Geographieunterricht in der DDR genutzt wurde, um geopolitische Interessen des Staates zu kommunizieren und zu verbreiten. Damit lässt sich durch die detaillierte Analyse des Fachunterrichts auch die Frage beantworten, ob SchülerInnen im Unterricht politisch manipuliert wurden und welche Handlungsmöglichkeiten die zentralen Akteure des Unterrichts, die LehrerInnen und die SchülerInnen, im Rahmen der durch die Bildungspolitik gesetzten curricularen Vorgaben wahrgenommen haben.