Speziell in Anwendungen mit intensiver Temperatur- und Korrosionsbeanspruchung finden vermehrt Phosphate als sogenannte chemische Binder für Hochleistungskeramiken Verwendung. Konkret ist die Summe der Reaktionsverläufe während des Bindemechanismus in Folge einer thermisch-induzierten Aushärtung und somit die Wirkungsweise von Phosphatbindern prinzipiell innerhalb der Fachliteratur nicht eindeutig untersucht. Innerhalb dieser Arbeit wurden aufbauend auf einer umfangreichen strukturanalytischen Prüfungsanordnung (Festkörper-NMR, RBA, REM-EDX) einer exemplarischen phosphatgebundenen Al₂O₃-MgAl₂O₄-Hochtemperaturkeramikzusammensetzung unter Einbeziehung verschiedenartiger anorganischer Phosphate grundlegende Bindemechanismen charakterisiert. Mechanisch-physikochemische Eigenschaftsuntersuchungen (STA, Dilatometrie, DMA, KBF) deckten zudem den Einfluss der eingesetzten Phosphate auf die Eigenschaftsentwicklungen der Feuerfestkeramiken bezüglich des Abbindeverhaltens, der Biegefestigkeit sowie der thermischen Längenänderung auf, welche mit Strukturänderungen korreliert wurden. Es wurde gezeigt, dass sich Bindemechanismen bei Verwendung von Phosphaten temperaturgeleitet (20 °C ≤ T ≤ 1500 °C) grundsätzlich aus zwei parallel ablaufenden Reaktionsabfolgen zusammensetzen, wobei die sich entwickelnden Phosphatphasen innerhalb der Keramikmasse quantitativ und qualitativ bezüglich ihrer Bindewirkung bewertet wurden. Zum einen wurde die Bildung eines festigkeitssteigernden Bindenetzwerks aus Aluminiumphosphaten meist amorpher Struktur identifiziert und charakterisiert. Dieses bindungsfördernde, dreidimensionale Aluminiumphosphatnetzwerk baut sich innerhalb der Initialisierungs- und Vernetzungsphasen temperaturgeleitet kontinuierlich über multiple Vernetzungsreaktionen homogen auf. Zum anderen werden Reaktionsabfolgen durch parallel ablaufende Strukturumwandlungen nicht aktiv-bindender Phosphatspezies wie Magnesium-, Calcium- oder Zirkoniumphosphate ergänzt, welche lediglich thermische Umwandlungsreaktionen der Ausgangsphosphate darstellen. Vermehrt bei T > 800 °C geht das phosphatische Bindenetzwerk Festkörperreaktionen mit MgAl₂O₄ unter Ausbildung und Agglomeration von Magnesium-Orthophosphat-Sinterstrukturen ein. Die Bildung dieser niedrigschmelzenden Hochtemperaturphasen führt zu einem teilweisen Bruch des Bindenetzwerks.

Amphibian populations are declining worldwide for multiple reasons such as habitat destruction and climate change. An example for an endangered European amphibian is the yellow-bellied toad Bombina variegata. Populations have been declining for decades, particularly at the northern and western range margin. One of the extant northern range centres is the Westerwald region in Rhineland-Palatinate, Germany. To implement informed conservation activities on this threatened species, knowledge of its life-history strategy is crucial. This study therefore focused on different developmental stages to test predictions of life-history theory. It addressed (1) developmental, (2) demographic and (3) genetic issues of Bombina variegata as a model organism: (1) Carry-over effects from larval environment to terrestrial stages and associated vulnerability to predators were investigated using mesocosm approaches, fitness tests and predation trials. (2) The dynamics and demography of B. variegata populations were studied applying a capture-mark-recapture analysis and skeletochronology. The study was complemented through (3) an analysis of genetic diversity and structuring of B. variegata populations using 10 microsatellite loci. In order to reveal general patterns and characteristics among B. variegata populations, the study focused on three geographical scales: local (i.e. a former military training area), regional (i.e. the Westerwald region) and continental scale (i.e. the geographical range of B. variegata). The study revealed carry-over effects of larval environment on metamorph phenotype and behaviour causing variation in fitness in the early terrestrial stage of B. variegata. Metamorph size and condition are crucial factors for survival, as small-sized individuals were particularly prone to predator attacks. Yellow-bellied toads show a remarkable fast-slow continuum of the life-history trait longevity. A populations’ position within this continuum may be determined by local environmental stochasticity, i.e. an extrinsic source of variation, and the efficiency of chemical antipredator protection, i.e. an intrinsic source of variation. Extreme longevity seems to be an exception in B. variegata. Senescence was absent in this study. Weather variability affected reproductive success and thus population dynamics. The dispersal potential was low and short-term fragmentation of populations caused significant genetic differentiation at the local scale. Long-term isolation resulted in increased genetic distance at the regional scale. At the continental scale, populations inhabiting the marginal regions were deeply structured with reduced allelic richness. As consequence of environmental changes, short-lived and isolated B. variegata populations at the range margin may face an increased risk of extinction. Conservation measures should thus improve the connectivity among local populations and reinforce annual reproductive success. Further research on the intraspecific variation in B. variegata skin toxins is required to reveal potential effects on palatability and thus longevity.

Die Wirbelsäule als tragende Säule des menschlichen Körpers ist bei vielen Bewegungsabläufen hohen Belastungen ausgesetzt. Fehl- und Überbelastungen rufen dabei oft dauerhafte Schädigungen hervor. Daher ist es von Interesse, die innerhalb der Wirbelsäule auftretenden Belastungen zu bestimmen. Eine moderne und zuverlässige Methode zur Belastungsbestimmung ist der Aufbau eines Berechnungsmodells. In der vorliegenden Arbeit wurde ein Mehr-Körper-System (MKS) Modell der Lendenwirbelsäule erstellt. Mit Hilfe des Modells können sowohl die übertragenen Kräfte und Momente in allen inneren Strukturen berechnet als auch die Kinematik des Bewegungsablaufs simuliert werden. Die Grundstruktur des Modells bilden die als Starrkörper angenommenen knöchernen Strukturen der fünf Lendenwirbel L1 bis L5, des Os Sacrums und des Os iliums, die über die Segmentierung eines CT-Datensatzes des Abgusses der Wirbeloberflächen eines durchschnittlich großen Europäers gewonnen wurden. Die elastischen Elemente der Wirbelsäule wurden unter Berücksichtigung ihrer physikalischen Eigenschaften in das Modell implementiert. Grundlage für die Modellierung der Zwischenwirbelscheiben waren dabei eigens durchgeführte experimentelle Messungen. Das charakteristische Kraft-Deformations-Verhalten der Ligamente wurde der Literatur entnommen. Die Umsetzung im Computermodell berücksichtigt neben dem physikalischen Verhalten eines einzelnen Ligamentes zusätzlich durch einen Gewichtungsfaktor das Zusammenspiel aller Ligamente im komplex aufgebauten Ligamentapparat. Die Facettengelenke wurden durch Kontaktmodellierung in den Knorpelschichten realisiert. Daneben wurde ein Modell eines Implantatsystems entwickelt, das zur dynamischen Stabilisierung der Lendenwirbelsäule genutzt wird. Die Validierung der erstellten Modelle erfolgte über den Vergleich mit In-Vitro erhobenen Daten. Betrachtet wurden neben der intakten Wirbelsäule zudem degenerative Schädigungen der Zwischenwirbelscheibe und deren operative Versorgung durch Nukleotomie und dynamische Stabilisierung. Die Ergebnisse der Simulationen zeigen dabei eine sehr gute Näherung an die experimentell ermittelten Messwerte. Durch Anwendung der Computermodelle konnten die Auswirkungen verschiedener operativer Eingriffe, wie Interlaminotomie, Hemilaminektomie und Laminektomie auf die unterschiedlichen Strukturen der Lendenwirbelsäule berechnet werden. Ein weiteres Anwendungsgebiet lag in der Untersuchung des momentanen Drehzentrums. Neben der Bestimmung der Drehpunktbahn bei intakter Wirbelsäule konnten die Effekte einer degenerativ geschädigten und operativ versorgten Zwischenwirbelscheibe auf den Verlauf des momentanen Drehzentrums berechnet und simuliert werden.

The first group that was revised within my study is Ochralea Clark, 1865 (Hazmi & Wagner 2010a). I have checked the type specimen of most species that were originally described in Ochralea and there is no doubt that this genus is clearly distinct from Monolepta. Weise (1924) has synonymised Galeruca nigripes (Olivier, 1808) with O. nigricornis Clark, 1865 and the valid name of the species is O. nigripes (Olivier, 1808). Out of ten species originally described in this genus, only this species remain valid and O. pectoralis is a new synonym of O. nigripes. Additionally, Monolepta wangkliana Mohamedsaid, 2000 is very closely related to O. nigripes and need to be transferred to Ochralea. The second genus where the revision is still published is Arcastes Baly, 1865 (Hazmi & Wagner 2010b). I have checked the genitalic characters of A. biplagiata, and most of the type species of other Arcastes. Arcastes biplagiata possesses a peculiar shape of the median lobe and asymmetrically arranged endophallic structures. These peculiar characters are very useful to delimit this genus from the others. Therefore, only three valid species remain in Arcastes, while two new synonyms are found and fourrnother species need to be transferred to other genera. While checking the genitalic characteristics of type species of Arcastes sanguinea, thernmedian lobe as well as the spermatheca of this species possesses strong differences to A. biplagiata. The species was redescribed and transferred in a monotypic new genus Rubrarcastes Hazmi & Wagner, 2010c. The fourth genus that was already revised is Neolepta Jacoby, 1884. It was originally described on base of only two species by that time, N. biplagiata and N. fulvipennis. Jacoby has not designated a type species of the genus, and Maulik (1936) did it later, with the designation of N. biplagiata. Jacoby in his original description has only commented that Neolepta is very close and similar to Monolepta Chevrolat, 1837 and Candezea Chapuis, 1879. Subsequent authors have described further eight species, and transferred one species from Luperodes to it, summing up the total number of eleven described species in Neolepta. I have checked the genitalic characters of the type, N. biplagiata and have found out that the median lobe is not incised apically and stronger sclerotised ventral carinae with an apical hook close to the apex occur. Out of all described species, only two are closely related to the genero-type, N. sumatrensis (Jacoby, 1884) new combination and N. quadriplagiata Jacoby, 1886 that will remain in this group after the revision. All other species need to be transferred to other genera, including the newly described Paraneolepta and Orthoneolepta. The last distinct paper of this thesis presented the results on Monolepta Chevrolat, 1837. The massive number of Monolepta from the entire Oriental Region, with about 260 described species names is a more long-life project and not practicable within a PhD-study. Thus I have focused on the species of Monolepta known from the Sundaland area in this work. A comprehensive revision including the study of the primary types of the described species, has never been done for Monolepta from this sub-region, while new species have also been described in the last decade (e. g. Mohamedsaid 1993, 1997, 1998, 1999, 2000a,b, 2001, 2002, 2005). On base of the most current species lists of Mohamedsaid (2001, 2004, 2005) and Kimoto (1990), the number of valid species described from this region is about 72. After my revision, only thirteen valid species can remain in Monolepta in the sense of the generotype M. bioculata (Wagner 2007), while seven species have been found as new synonyms, three have been already transferred to other genera and further 49 species need to be transferred to other genera.

Habitat loss and fragmentation due to climate and land-use change are among the biggest threats to biodiversity, as the survival of species relies on suitable habitat area and the possibility to disperse between different patches of habitat. To predict and mitigate the effects of habitat loss, a better understanding of species dispersal is needed. Graph theory provides powerful tools to model metapopulations in changing landscapes with the help of habitat networks, where nodes represent habitat patches and links indicate the possible dispersal pathways between patches. This thesis adapts tools from graph theory and optimisation to study species dispersal on habitat networks as well as the structure of habitat networks and the effects of habitat loss. In chapter 1, I will give an introduction to the thesis and the different topics presented in this thesis. Chapter 2 will then give a brief summary of tools used in the thesis. In chapter 3, I present our model on possible range shifts for a generic species. Based on a graph-based dispersal model for a generic aquatic invertebrate with a terrestrial life stage, we developed an optimisation model that models dispersal directed to predefined habitat patches and yields a minimum time until these patches are colonised with respect to the given landscape structure and species dispersal capabilities. We created a time-expanded network based on the original habitat network and solved a mixed integer program to obtain the minimum colonisation time. The results provide maximum possible range shifts, and can be used to estimate how fast newly formed habitat patches can be colonised. Although being specific for this simulation model, the general idea of deriving a surrogate can in principle be adapted to other simulation models. Next, in chapter 4, I present our model to evaluate the robustness of metapopulations. Based on a variety of habitat networks and different generic species characterised by their dispersal traits and habitat demands, we modeled the permanent loss of habitat patches and subsequent metapopulation dynamics. The results show that species with short dispersal ranges and high local-extinction risks are particularly vulnerable to the loss of habitat across all types of networks. On this basis, we then investigated how well different graph-theoretic metrics of habitat networks can serve as indicators of metapopulation robustness against habitat loss. We identified the clustering coefficient of a network as the only good proxy for metapopulation robustness across all types of species, networks, and habitat loss scenarios. Finally, in chapter 5, I utilise the results obtained in chapter 4 to identify the areas in a network that should be improved in terms of restoration to maximise the metapopulation robustness under limited resources. More specifically, we exploit our findings that a network’s clustering coefficient is a good indicator for metapopulation robustness and develop two heuristics, a Greedy algorithm and a deducted Lazy Greedy algorithm, that aim at maximising the clustering coefficient of a network. Both algorithms can be applied to any network and are not specific to habitat networks only. In chapter 6, I will summarize the main findings of this thesis, discuss their limitations and give an outlook of future research topics. Overall this thesis develops frameworks to study the behaviour of habitat networks and introduces mathematical tools to ecology and thus narrows the gap between mathematics and ecology. While all models in this thesis were developed with a focus on aquatic invertebrates, they can easily be adapted to other metapopulations.