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Supporting fish populations by restocking with artificially bred young fish is a common practice worldwide, which may sometimes have a negative effect on natural genetic diversity. In this study, the currently ongoing restocking program of brown trout (Salmo trutta Linnaeus, 1758) in the subarctic Pasvik river in Norway was investigated. Previous investigations of this population showed a loss of genetic diversity and both genetic and morphological differentiation between historical breeding stocks and wild trout populations. However, the genetic impact of the breeding program used in this river today has never been investigated. To accomplish this, I compared the parent fish, the offspring, and fish caught in the river using 16 short tandem repeat loci and estimated pairwise relatedness, inbreeding, genetic distances, and differentiation. The results showed, by estimating the effective population size, that the number of parents used in the breeding program was generally insufficient to maintain a genetically sustainable river population. Further, genetic diversity in stocked fish was typically not maximized due to lack of performing all possible crossings between males and females. In combination, this induced genetic drift in the offspring generations and thus genetic differentiation away from the river populations. In summary, the results from this study show that the current stocking practises used in the Pasvik river are not sustainable and that measures need to be taken to prevent continued loss of genetic diversity in this large-growing trout population.

O principal objetivo deste estudo foi investigar os processos responsáveis pela evolução morfológica craniana de primatas da subordem Strepsirrhini, com maior ênfase ao clado endêmico à ilha de Madagascar. Sistemas multidimensionais morfológicos como o crânio descrevem a quantidade de variação disponível para atuação de processos evolutivos. A partir de 27 marcos anatômicos cranianos e 39 distâncias euclidianas estimei matrizes de variância e covariância fenotípicas (Matrizes P) para 40 espécies das sete famílias viventes de Strepsirrhini e duas espécies do gênero Tarsius. Utilizei a abordagem da genética quantitativa para investigar o padrão de variação nas matrizes P dessa linhagem de primatas, conjuntamente com um par de matrizes fenotípica e genética de Saguinus fuscicolis. Para investigar a estabilidade e conservção do padrão da estrutura de variação ao longo da diversidade deste clado de primatas compararei estas matrizes através de dois métodos complementares que me permitiram avaliar a distribuição da variação no morfoespaço (Random Skewers) e o compartilhamento de direções de variação (Krzanowski) das matrizes. Os resultados obtidos sugerem uma estabilidade das matrizes, possivelmente mantida por seleção estabilizadora interna comum ao clado, aos demais primatas e mamíferos em geral. Esses resultados de comparação de matrizes são apresentados no Capítulo 1 e corroboram a conjectura de Cheverud, indicando que as matrizes cumprem o pressuposto de similaridade estrutural entre as matrizes P e a matriz G. Além disso o padrão de variação apresentou um sinal filogenético e algumas das diferenças observadas nas matrizes parecem estar relacionadas com fatores de dieta. No Capítulo 2 investiguei a evolução da divergência morfológica craniana em um conjunto de 70 espécies, onde testei a hipótese nula de deriva genética como explicação suficiente para a divergencia entre as médias das espécies. Esta hipótese foi avaliada dentro das expectativas de modelos da genética quantitativa através de duas metodologias. Tais testes avaliam a proporcionalidade de variação dentro (W) e entre grupos (B) sob perspectivas complementares. Com o teste de regressão investiguei a manutenção da quantidade de variação associada a cada eixo de variação, e com o teste de correlação avaliei o alinhamento entre estes eixos. Rejeitamos a H_0 em diversos pontos da árvore que representam eventos de cladogenese a nível de família e gênero. Nestes casos aceitamos a H_1 de seleção natural e vemos que a maior parte da diversificação da linhagem de primatas de Madagascar foi influenciada por seleção direcional envolvendo tamanho e alterações anatômicas relacionadas a dieta / The main goal of this study was to investigate the evolutionary processes responsible for Strepsirrhini cranial morphological evolution. Multidimensional morphological structures like the cranium can describe the amount of variance available to evolution. We used 27 landmarks and 39 euclidean distances between them to describe the variation in the cranium. We used a broad phylogenetic scaled comparison of cranial P matrices representing 40 species of Strepsirrhini primates combined to a pair of Saguinus fuscicolis G and P to investigate the stability of variance structure along this lineage. Our results show a relative stability in the patterns of variance and covariance of the clade and that P matrices can be considered as surrogates to its underling G. We also report a high association between matrix similarity and phylogenetic distance. We investigated particular contributions of each trait to matrix dissimilarity through a evolutionary perspective considering the main dietary shifts observed in the clade. Our results suggest that differences in observed patterns of variation can be attributed to characters with heterogeneity in the degree of stabilizing selection in the adult cranium and to differences in directional selection involved in chewing of specialized feeding behavior. Under the quantitative genetics theory lies an expectation for the evolution of average phenotypes that if populations have diverged by random processes, patterns of within and between-taxon morphological variation should be proportional. In chapter 2 we tested the null hypothesis that genetic drift is a sufficient explanation to observed divergence in cranial multivariate means of 70 Strepsirrhini primates. We detected deviations from neutrality along the whole clade of Strepsirrhini and specially in more inclusive nodes. We argue that this deviations reflect important historical shifts in the evolution of the clade associated with directional selection for size and in anatomical features related with diet

<p>In this thesis the genetic variation of two grouse species, the Chinese grouse (<i>Bonasa sewersowi</i>) and the Black grouse (<i>Tetrao tetrix</i>) was examined with neutral genetic markers: microsatellites. Habitat fragmentation and isolation leads to structuring among and loss of genetic variation within populations.</p><p>The Chinese grouse in a small population in Lianhuasan nature reserve was found to have undergone a population bottleneck and as a result of isolation and possible inbreeding showed genetic impoverishment hereof.</p><p>The Black grouse populations in Europe face various different conditions from widely distributed areas of suitable habitat in the northern and eastern parts of its range to highly naturally and anthropogenically fragmented habitat landscapes in the west.</p><p>Structure among populations was found in Great Britain where Wales, Scotland and England showed characteristics of three different genetic entities, indicating very little or no geneflow between these populations. </p><p>The Dutch population showed signs of loss of genetic variation as to be expected from a population that has historically decreased in population size from several thousands to tens of individuals in a matter of decades. However the possibility to spot signs of a bottleneck was impaired due to the short time-window in which this can be observed in a population with such a low effective population size (N_E).</p><p>The sampled populations in Europe clustered into five different groups of genetic identities. The different clusters were: Great Britain-, the Netherlands-, Fenno-Scandian-, Alpine- and lowland German-Austrian populations. The level of genetic variation when compared over all these different populations decreased as a sign of isolation and small N_E. However it was not feasible to separate the impact of these two factors.</p>

<p>To shed light on forces that shape the molecular evolution of bird genomes, and in turn avian adaptations, comparative analyses of avian DNA sequences are important. Moreover, contrasting findings in birds to those of other organisms will lend a clearer view on general aspects of molecular evolution. However, few such analyses have been conducted in birds. Progress is presented in this thesis.</p><p>Theories predict a reduction in the mutation rate of the Z chromosome as the harmful effects of recessive mutations are exposed in female birds. We find no evidence for this. Instead, the substitution rates of sex chromosomes and autosomes are largely compatible with expectations from male-biased mutation. This suggests that a majority of mutations arise during DNA replication.</p><p>Substitution rates also vary across chicken autosomes. For instance, microchromosomes accumulate ~20% more substitutions than macrochromosomes. We show that a majority of the autosomal variation in substitution rate can be accounted for by GC content, mainly due to the incidence of mutable CpG-dinucleotides.</p><p>Sequence comparisons also show that the pattern of nucleotide substitution varies in the chicken genome and this reinforces regional differences in base composition. </p><p>The level of selective constraint in at least some avian lineages is higher than in mammalian lineages as indicated by low<i> d</i><i>N</i><i>/d</i><i>S</i><i> </i>– ratios. Larger historical population sizes of birds relative to mammals could explain this observation. Within the avian genome, the<i> d</i><i>N</i><i>/d</i><i>S</i> is lower for genes on micro- than macrochromosomes, potentially owing to a higher incidence of house-keeping genes in the former category.</p><p>Contrasting data on non-synonymous and synonymous substitution for divergence and polymorphism shows that positive selection has contributed more to the evolution of Z-linked than autosomal genes. This is likely explained by the full exposure of beneficial recessive mutations on Z when in female birds.</p>

Genetic mapping contributes to the understanding of functional mechanisms that underlie the constitution of living organisms and their physiology. For example, genetic mapping can be used in conceiving new treatments of congenital or infectious diseases and in selecting plants and animals that have a higher and better production. The most common approaches of genetic mapping exploit the allelic segregation in a pedigree during only a few number of generations and, consequently, they do not have a sufficient resolution to allow an effective gene isolation and cloning. An alternative to these approaches is to study allelic associations along the history of a population. This requires accurate models of population demography, genetic inheritance and allelic associations. This thesis contributes to the modelling of allelic associations (linkage disequilibrium, LD) and to the assessment of the effects of selection and inbreeding. In a simulation framework, we fitted the multimarker-multiallelic LD with an exponential function characterised by two parameters: the distance (R) at which LD is independent of the genetic distance and the LD reached at this distance (residual LD, rs). As an application of this approach, the LD was estimated in five populations of pigs. We observed a long range LD (>10cM) that was explained by the random drift. Moreover, significantly increased LD was found in regions harbouring selected QTL (quantitative trait loci), suggesting an effect of selection. Fitting LD with the exponential model proposed in simulations indicated that mapping methods using LD (LDM) can achieve a resolution of ~3cM in the populations of pigs we have studied and can be powerful with a marker spacing of 5-10cM. As illustrated with these data from pigs, the model that we used to fit LD offers opportunities to characterise allelic association in populations, estimate the required marker density for genome-wide LD studies and determine the expected resolution of LDM. It is also shown that the proposed model can help overcoming the assumptions of asymptotic linkage equilibrium and independence between markers that are commonly made in LDM but are not always fulfilled.

In this thesis the genetic variation of two grouse species, the Chinese grouse (Bonasa sewersowi) and the Black grouse (Tetrao tetrix) was examined with neutral genetic markers: microsatellites. Habitat fragmentation and isolation leads to structuring among and loss of genetic variation within populations. The Chinese grouse in a small population in Lianhuasan nature reserve was found to have undergone a population bottleneck and as a result of isolation and possible inbreeding showed genetic impoverishment hereof. The Black grouse populations in Europe face various different conditions from widely distributed areas of suitable habitat in the northern and eastern parts of its range to highly naturally and anthropogenically fragmented habitat landscapes in the west. Structure among populations was found in Great Britain where Wales, Scotland and England showed characteristics of three different genetic entities, indicating very little or no geneflow between these populations. The Dutch population showed signs of loss of genetic variation as to be expected from a population that has historically decreased in population size from several thousands to tens of individuals in a matter of decades. However the possibility to spot signs of a bottleneck was impaired due to the short time-window in which this can be observed in a population with such a low effective population size (NE). The sampled populations in Europe clustered into five different groups of genetic identities. The different clusters were: Great Britain-, the Netherlands-, Fenno-Scandian-, Alpine- and lowland German-Austrian populations. The level of genetic variation when compared over all these different populations decreased as a sign of isolation and small NE. However it was not feasible to separate the impact of these two factors.

To shed light on forces that shape the molecular evolution of bird genomes, and in turn avian adaptations, comparative analyses of avian DNA sequences are important. Moreover, contrasting findings in birds to those of other organisms will lend a clearer view on general aspects of molecular evolution. However, few such analyses have been conducted in birds. Progress is presented in this thesis. Theories predict a reduction in the mutation rate of the Z chromosome as the harmful effects of recessive mutations are exposed in female birds. We find no evidence for this. Instead, the substitution rates of sex chromosomes and autosomes are largely compatible with expectations from male-biased mutation. This suggests that a majority of mutations arise during DNA replication. Substitution rates also vary across chicken autosomes. For instance, microchromosomes accumulate ~20% more substitutions than macrochromosomes. We show that a majority of the autosomal variation in substitution rate can be accounted for by GC content, mainly due to the incidence of mutable CpG-dinucleotides. Sequence comparisons also show that the pattern of nucleotide substitution varies in the chicken genome and this reinforces regional differences in base composition. The level of selective constraint in at least some avian lineages is higher than in mammalian lineages as indicated by low dN/dS – ratios. Larger historical population sizes of birds relative to mammals could explain this observation. Within the avian genome, the dN/dS is lower for genes on micro- than macrochromosomes, potentially owing to a higher incidence of house-keeping genes in the former category. Contrasting data on non-synonymous and synonymous substitution for divergence and polymorphism shows that positive selection has contributed more to the evolution of Z-linked than autosomal genes. This is likely explained by the full exposure of beneficial recessive mutations on Z when in female birds.

Uncovering and understanding the processes that have led to the biological diversity we observe today are of fundamental interest in biology. Since direct observation of speciation is usually impossible, knowledge about the processes behind species formation can be gathered by studying mutations, natural/sexual selection, and genetic drift. In this thesis I aim to identify evolutionary processes that cause species divergence and, ultimately, speciation using Swedish cyprinid fish as a model system. Assuming that the demographic history of a population is mirrored in the genome, I studied the effects of a bottleneck on genetic variability in populations of roach. As expected, I found that a decrease in population size caused a decrease in genetic variability, a pattern that was obtained from both microsatellite and mitochondrial data. The importance of hybridization for speciation is debated, however, by analyzing morphology and microsatellites I could show that common bream and white bream and their interspecific hybrids are phenotypically and genetically differentiated and that ongoing geneflow is mainly unidirectional. Ongoing geneflow antagonizes the effect of genetic drift, but by studying isolated populations (= no gene flow) the impact of genetic drift can be assessed. Long-term isolated populations of roach and perch surprisingly showed stable levels of genetic diversity over time despite decreasing effective population size. However, each population genetically diverged during the period of investigation, a finding that is consistent with the effect of drift. An analysis of the systematic relationship of the 18 species of Swedish cyprinids revealed low congruence of phylogenies based on two different genetic markers. The position of the tench remains unresolved and the relationship of common bream and white bream as sister species cannot be confirmed. Within cyprinid fishes, diversification rates reveal a slowdown with time, a pattern that I found also in other fish clades and that is consistent with density-dependent cladogenesis. Overall, based on the findings presented in this thesis I emphasize that the maintenance of genetic variation in populations is essential since genetic variation is the key element for processes of divergence to act upon.

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