<p>This thesis investigates paper structure and how its spatial heterogeneity affects the electrostatic and contact forces responsible for the toner transfer in Xerographic printing. Modeling predictions and experiments are reported which link length scales of variation in toner density distribution in Xerographic printing with certain structural length scales in paper.</p> <p>A modified 3D fibre network model is introduced, which is used to simulate handsheet paper microstructure. Specific measures addressed by the model include formation, surface roughness and porosity. Simulated (i.e. virtual) handsheet paper structure is compared with that from specially prepared laboratory handsheet, obtaining a good correspondence between theory and experiments.</p> <p> An efficient Multigrid Poisson solver is used to simulate the electrostatic fields involved in the Xerographic toner transfer process. The distribution of dielectric property is input into the solver either analytically or from simulated 3D paper webs prepared by the fibre network model of paper. A spectral analysis is used to elucidate the relative importance of spatial variations of paper surface, filler and porosity in establishing spatial variations of the electrostatic field. It is found that only long wavelength variations in either surface height, bulk filler or porosity affect variations in electrostatic toner transfer forces to any relevant degree. Furthermore, it is shown that the long wavelength perturbations of the electrostatic field can be modeled using a new 1D effective capacitor model. Direct use of simulated handsheet paper webs - which are described by several heterogeneous measures - shows that to lowest order it is the paper surface structure not formation is responsible in shaping the electrostatic toner field variations.</p> <p> A new platform for modeling toner transfer in Xerographic printing is also introduced. It combines the 3D stochastic fibre network model of paper, the 3D electrostatic field solver, paper compression in the printing nip, and contact adhesion forces acting on toner particles during Xerographic printing. The modeling platform is used to demonstrate that paper-press interactions are critical in shaping the surface of paper, which, in turn, has the greatest influence in controlling both the electrostatic and contact adhesion forces responsible for shaping the distribution of toner transferred to paper during Xerography.</p> / Thesis / Doctor of Philosophy (PhD)

The Caledonian pinewoods are a habitat of crucial environmental and cultural importance, and the sole home of many rare species. However, they have seen steady decline in recent centuries, through the establishment of hunting estates and forestry plantations. A recent trend in management is the attempted transformation of existing plantations (dense communities with a regular spatial structure and low variance in size and age) towards a state mimicking the perceived natural condition, which has a lower density, irregular spatial pattern, high variance in size and age. This presents a problem for traditional forestry practices, which were conceived primarily with “even-aged” plantation populations in mind. The shift towards management of an uneven-aged structure requires a more in-depth consideration of individual trees’ lifecycles and their effect upon long-term population dynamics. In recent years, great advances in computational and mathematical models for spatially interacting populations have been made. However, certain complications have prevented them from being utilised to their full potential for the purposes of forest management. Forest communities are not only spatially structured; the size of each tree plays a role in its ability to acquire resources for growth and survival. Existing models of population dynamics are discussed, and their extension to incorporate both size- and spatially- structured interactions is presented. The key aspects of populations’ structural development are studied. Data from both plantation and semi-natural Scots Pine stands in Scotland allow parameterisation of a stochastic individual-based model, which in turn provides insights into the behaviour of real populations, and the importance of spatial effects and heterogeneity in individuals. A partial differential equation (moment) approximation to the stochastic model is presented. While this is analytically intractable, numerical integration and heuristic analysis of the equations enable clearer identification of the drivers of population structure. Many results are concordant with existing models of both qualitative forest stand development and theoretical dynamics of spatially-structured populations, while others are specific to joint size-space structure. This deeper understanding of the population dynamics allows robust recommendations for diverse uneven-aged stand management objectives to be made. Approaches to accelerating the transformation of plantation stands towards a “natural” state (using two key operations: thinning – removal of trees, and planting) are investigated. Finally, approaches to so-called “continuous cover forestry” – the practice of maintaining a quasi-natural state while also obtaining economic value from a forest – are also considered. In both cases, the model’s simplicity enables clearer conclusions than would be possible using other approaches.

The subject of the diploma thesis is the design and structural assessment of the load-bearing steel structure of the airport terminal located in Pardubice. Te project is designed in two variants. The dimensions of the foor plan are 83,2x54,295 m. The maximum height of the terminal is 14,662 m.The load-bearing structure consist of a eleven spatial frames at an axial distance of 8,0 m. The spacial rigidity of the structure is ensured by a system of sway and longitudinal bracings.

La diversification des signaux aposématiques dans un cadre de mimétisme müllérien est un phénomène intrigant. Alors que la théorie relative à l'aposématisme et au mimétisme suggère l'évolution vers un signal aposématique unique, d'impressionnantes variations peuvent être observées entre les populations, et cela à petite échelle spatiale. Il a été supposé que la variation spatiale des pressions de sélection engendrées par différents prédateurs puisse être à l'origine de ce phénomène. Afin de tester cette hypothèse, nous avons étudié la transition entre deux systèmes géographiques caractérisés par des patrons aposématiques distincts chez des grenouilles mimétiques et toxiques du nord du Pérou (Dendrobatidae) en combinant les outils de génétique des populations aux outils écologiques. Dans chacun de ces systèmes, Ranitomeya imitator vit en sympatrie avec R. ventrimaculata ou R. variabilis. Il s'agit du principal exemple empirique suggérant que dans un cadre de mimétisme müllérien, il n'y a pas convergence des signaux aposématiques des deux espèces, mais plutôt convergence unidirectionnelle où R. imitator, étant polymorphe, imite des espèces monomorphes avec lesquelles elle est sympatrique. Premièrement, les résultats réfutent les prémisses qui suggèrent que R. imitator converge vers le signal aposématique d’une autre espèce. La haute similarité génétique entre les espèces modèles suggère qu'elles ont divergé plus récemment que les populations de R. imitator ou qu'elles sont encore connectées par du flux génique. Ces résultats indiquent que ces espèces ont été identifiées à tort comme des espèces différentes. De fait, l'identification de l'espèce imitatrice basée sur la variabilité phénotypique est invalidée dans ce système puisque R. imitator et R. variabilis/ventrimaculata démontrent la même variabilité. Deuxièmement, nos résultats démontrent que la prédation varie spatialement, autant en intensité qu'en direction, créant ainsi un paysage hétérogène de pressions de sélection. Ainsi, de fortes pressions de prédation stabilisatrice permettent le maintien de l'organisation géographique de différents signaux aposématiques et expliquent l'uniformité de ces signaux ainsi que les relations mimétiques. Par contre, le relâchement temporaire des pressions de prédation permet l'apparition de nouveaux phénotypes aposématiques via les processus évolutifs neutres, conduisant à un haut polymorphisme au niveau de ces populations. L'interaction de ces modes sélectifs nous a permis de démontrer pour la première fois comment la théorie évolutive de Wright (shifting balance theory) permet la diversification adaptative dans un système naturel. Pour conclure, cette étude a permis de mettre en évidence à quel point les systèmes de mimétisme müllérien peuvent être dynamiques. L'alternance spatiale entre les processus évolutifs neutres et la sélection naturelle permet l'émergence de nouveaux phénotypes aposématiques à une échelle locale, ainsi que l'apparition d'une organisation géographique des signaux d'avertissement et des relations de mimétisme müllérien. / The diversification of aposematic signals in Müllerian mimicry systems is a puzzling phenomenon. Although aposematism and mimicry are expected to promote uniformity in warning signals, impressive variations may be observed among populations at relatively small spatial scales. It has been suggested that spatial variation in selective pressures caused by predators might be responsible for this phenomenon. In order to test this hypothesis, we studied the transition in the aposematic signals of the mimetic poison-dart frogs of Northern Peru (Dendrobatidae) between two geographical systems characterized by distinct aposematic signals. This was done by combining population genetics and ecological tools. In both systems, Ranitomeya imitator is sympatric with either R. ventrimaculata or R. variabilis. This system is recognized as a rare example in support of the hypothesis for advergence: R. imitator, which is polymorphic, is believed to mimic distinct sympatric monomorphic model species. However, our results do not support the hypothesis for advergence of the aposematic signals by R. imitator. The genetic similarity between the model species suggests that they have diverged more recently than R. imitator populations or that they are still connected by gene flow. These results indicate that these species were misidentified as being different species. As such, the identification of the mimetic species based on phenotypic variability is invalidated in this system, since R. imitator is as variable as R. variabilis/ventrimaculata. Also, our results demonstrate that predation pressure is spatially variable, in both intensity and direction, thus creating a heterogeneous selective landscape. As such, strong and directed stabilizing selective pressures maintain the geographic organisation of aposematic signals and explain phenotypic uniformity and mimetic relationships. Relaxation of these selective pressures enables for the appearance of novel aposematic phenotypes and promotes high phenotypic variability via neutral evolutionary processes. The interaction between these selective regimes has enabled us to demonstrate, and this for the first time, how the Wright’s shifting balance theory of evolution may promote adaptive diversification in a natural system. In conclusion, this study highlights just how dynamic Müllerian mimicry systems can be. The interplay between neutral evolutionary processes and natural selection enables for the predominance of novel aposematic phenotypes at a local scale, and the geographical organisation of warning signals and Müllerian relationships.

La diversification des signaux aposématiques dans un cadre de mimétisme müllérien est un phénomène intrigant. Alors que la théorie relative à l'aposématisme et au mimétisme suggère l'évolution vers un signal aposématique unique, d'impressionnantes variations peuvent être observées entre les populations, et cela à petite échelle spatiale. Il a été supposé que la variation spatiale des pressions de sélection engendrées par différents prédateurs puisse être à l'origine de ce phénomène. Afin de tester cette hypothèse, nous avons étudié la transition entre deux systèmes géographiques caractérisés par des patrons aposématiques distincts chez des grenouilles mimétiques et toxiques du nord du Pérou (Dendrobatidae) en combinant les outils de génétique des populations aux outils écologiques. Dans chacun de ces systèmes, Ranitomeya imitator vit en sympatrie avec R. ventrimaculata ou R. variabilis. Il s'agit du principal exemple empirique suggérant que dans un cadre de mimétisme müllérien, il n'y a pas convergence des signaux aposématiques des deux espèces, mais plutôt convergence unidirectionnelle où R. imitator, étant polymorphe, imite des espèces monomorphes avec lesquelles elle est sympatrique. Premièrement, les résultats réfutent les prémisses qui suggèrent que R. imitator converge vers le signal aposématique d’une autre espèce. La haute similarité génétique entre les espèces modèles suggère qu'elles ont divergé plus récemment que les populations de R. imitator ou qu'elles sont encore connectées par du flux génique. Ces résultats indiquent que ces espèces ont été identifiées à tort comme des espèces différentes. De fait, l'identification de l'espèce imitatrice basée sur la variabilité phénotypique est invalidée dans ce système puisque R. imitator et R. variabilis/ventrimaculata démontrent la même variabilité. Deuxièmement, nos résultats démontrent que la prédation varie spatialement, autant en intensité qu'en direction, créant ainsi un paysage hétérogène de pressions de sélection. Ainsi, de fortes pressions de prédation stabilisatrice permettent le maintien de l'organisation géographique de différents signaux aposématiques et expliquent l'uniformité de ces signaux ainsi que les relations mimétiques. Par contre, le relâchement temporaire des pressions de prédation permet l'apparition de nouveaux phénotypes aposématiques via les processus évolutifs neutres, conduisant à un haut polymorphisme au niveau de ces populations. L'interaction de ces modes sélectifs nous a permis de démontrer pour la première fois comment la théorie évolutive de Wright (shifting balance theory) permet la diversification adaptative dans un système naturel. Pour conclure, cette étude a permis de mettre en évidence à quel point les systèmes de mimétisme müllérien peuvent être dynamiques. L'alternance spatiale entre les processus évolutifs neutres et la sélection naturelle permet l'émergence de nouveaux phénotypes aposématiques à une échelle locale, ainsi que l'apparition d'une organisation géographique des signaux d'avertissement et des relations de mimétisme müllérien. / The diversification of aposematic signals in Müllerian mimicry systems is a puzzling phenomenon. Although aposematism and mimicry are expected to promote uniformity in warning signals, impressive variations may be observed among populations at relatively small spatial scales. It has been suggested that spatial variation in selective pressures caused by predators might be responsible for this phenomenon. In order to test this hypothesis, we studied the transition in the aposematic signals of the mimetic poison-dart frogs of Northern Peru (Dendrobatidae) between two geographical systems characterized by distinct aposematic signals. This was done by combining population genetics and ecological tools. In both systems, Ranitomeya imitator is sympatric with either R. ventrimaculata or R. variabilis. This system is recognized as a rare example in support of the hypothesis for advergence: R. imitator, which is polymorphic, is believed to mimic distinct sympatric monomorphic model species. However, our results do not support the hypothesis for advergence of the aposematic signals by R. imitator. The genetic similarity between the model species suggests that they have diverged more recently than R. imitator populations or that they are still connected by gene flow. These results indicate that these species were misidentified as being different species. As such, the identification of the mimetic species based on phenotypic variability is invalidated in this system, since R. imitator is as variable as R. variabilis/ventrimaculata. Also, our results demonstrate that predation pressure is spatially variable, in both intensity and direction, thus creating a heterogeneous selective landscape. As such, strong and directed stabilizing selective pressures maintain the geographic organisation of aposematic signals and explain phenotypic uniformity and mimetic relationships. Relaxation of these selective pressures enables for the appearance of novel aposematic phenotypes and promotes high phenotypic variability via neutral evolutionary processes. The interaction between these selective regimes has enabled us to demonstrate, and this for the first time, how the Wright’s shifting balance theory of evolution may promote adaptive diversification in a natural system. In conclusion, this study highlights just how dynamic Müllerian mimicry systems can be. The interplay between neutral evolutionary processes and natural selection enables for the predominance of novel aposematic phenotypes at a local scale, and the geographical organisation of warning signals and Müllerian relationships.

Biodiversity is determined by a myriad of complex processes acting at different scales. Given the current rates of biodiversity loss and change, it is of paramount importance that we improve our understanding of the underlying structure of ecological communities. In this thesis, I focused on Species Abundance Distributions (SAD), as a synthetic measure of biodiversity and community structure, and on Beta (β) diversity patterns, as a description of the spatial variation of species composition. I systematically assessed the effect of scale on both these patterns, analysing a broad range of community data, including different taxa and habitats, from the terrestrial, marine and freshwater realms. Knowledge of the scaling properties of abundance and compositional patterns must be fully integrated in biodiversity research if we are to understand biodiversity and the processes underpinning it, from local to global scales. SADs depict the relative abundance of the species present in a community. Although typically described by unimodal logseries or lognormal distributions, empirical SADs can also exhibit multiple modes. However, the existence of multiple modes in SADs has largely been overlooked, assumed to be due to sampling errors or a rare pattern. Thus, we do not know how prevalent multimodality is, nor do we have an understanding of the factors leading to this pattern. Here, I provided the first global empirical assessment of the prevalence of multimodality across a wide range of taxa, habitats and spatial extents. I employed an improved method combining two model selection tools, and (conservatively) estimated that ~15% of the communities were multimodal with strong support. Furthermore, I showed that the pattern is more common for communities at broader spatial scales and with greater taxonomic diversity (i.e. more phylogenetically diverse communities, since taxonomic diversity was measured as number of families). This suggests a link between multimodality and ecological heterogeneity, broadly defined to incorporate the spatial, environmental, taxonomic and functional variability of ecological systems. Empirical understanding of how spatial scale affects SAD shape is still lacking. Here, I established a gradient in spatial scale spanning several orders of magnitude by decomposing the total extent of several datasets into smaller subsets. I performed an exploratory analysis of how SAD shape is affected by area sampled, species richness, total abundance and taxonomic diversity. Clear shifts in SAD shape can provide information about relevant ecological and spatial mechanisms affecting community structure. There was a clear effect of area, species richness and taxonomic diversity in determining SAD shape, while total abundance did not exhibit any directional effect. The results supported the findings of the previous analysis, with a higher prevalence of multimodal SADs for larger areas and for more taxonomically diverse communities, while also suggesting that species spatial aggregation patterns can be linked to SAD shape. On the other hand, there was a systematic departure from the predictions of two important macroecological theories for SAD across scales, specifically regarding logseries distributions being selected only for smaller scales and when species richness and number of families were proportionally much smaller than the total extent. β diversity quantifies the variation in species composition between sites. Although a fundamental component of biodiversity, its spatial scaling properties are still poorly understood. Here, I tested if two conceptual types of β diversity showed systematic variation with scale, while also explicitly accounting for the two β diversity components, turnover and nestedness (species replacement vs species richness differences). I provided the first empirical analysis of β diversity scaling patterns for different taxa, revealing remarkably consistent scaling curves. Total β diversity and turnover exhibit a power law decay with log area, while nestedness is largely insensitive to scale changes. For the distance decay of similarity analysis, while area sampled affected the overall dissimilarity values, rates of similarity were consistent across large variations in sampled area. Finally, in both these analyses, turnover was the main contributor to compositional change. These results suggest that species are spatially aggregated across spatial scales (from local to regional scales), while also illustrating that substantial change in community structure might occur, despite species richness remaining relatively stable. This systematic and comprehensive analysis of SAD and community similarity patterns highlighted spatial scale, ecological heterogeneity and species spatial aggregation patterns as critical components underlying the results found. This work expanded the range of scales at which both theories deriving SAD and community similarity studies have been developed and tested (from local plots to continents). The results here showed strong departures from two important macroecological theories for SAD at different scales. In addition, the overall findings in this thesis clearly indicate that unified theories of biodiversity (or assuming a set of synthetic minimal assumptions) are unable to accommodate the variability in SADs shape across spatial scales reported here, and cannot fully reproduce community similarity patterns across scales. Incorporating more realistic assumptions, or imposing scale dependent assumptions, may prove to be a fruitful avenue for ecological research regarding the scaling properties of SAD and community similarity patterns. This will allow deriving new predictions and improving the ability of theoretical models to incorporate the variability in abundance and similarity patterns across scales.

No description available.

In my diploma thesis the proposal is developed as supporting steel structure sports hall with dimensions 45 x 54 m, a maximum height of 15.5 meters,for the area of Znojmo. In a static calculation are designed and assessed the main bearing structural components such as solid panel purlins, spatial lattice truss, bracing and solid panel columns, which together with the truss form create a crosslinks, column bases and anchoring, plus Tribune.The work includes the design documentation consisting of a layout drawing, drawing anchoring and drawing selected details.