Introduction: Genetic determination of human face is clearly visible in family members. The resemblance between monozygotic twins who are genetically identical is especially remarkable. So far the possibilities of reliable prediction of the complex morphology of facial traits on the basis of genome analysis and the ability to capture the variability of human facial morphology through genotype variability are highly limited. Complete genetic basis of the physiological variability of craniofacial traits remains more or less unknown. This master's thesis was created as a pilot study of the shared project of the Laboratory of 3D Imagining and Analytical Methods and the Laboratory of Molecular Anthropology on Department of Anthropology and Human Genetics. Material and Methods: The specimen collection is composed of DNA samples derived from 30 families (29 with 4 members, 1 with 5 members) who fulfilled required criteria. Nine single nucleotide polymorphisms were chosen based on the available information. Eight of them are linked to normal facial variability and one was chosen based on the assumed function of the gene where the polymorphism is located. There were two methods of genotyping: RFLP method with the use of restriction endonuclease and SNaPshot method. Morphological data were provided by the...

ABSTRACT One cause of declines and extinctions of island species is carnivore introduction. Four carnivores, including the small Indian mongoose (Herpestes auropunctatus), are on the IUCN’s list of 100 of the World's Worst Invasive Alien Species. My thesis summarizes global patterns of carnivore introductions and examines ecological, evolutionary, and management impacts of this mongoose. I study abundances of reptiles and amphibians on mongoose-infested and mongoose-free islands in the Adriatic Sea to determine if factors other than mongoose presence can account for abundance differences. For several reptiles and amphibians, the mongoose is implicated as causing differences. Additionally, I assess species abundance in the small mammal community and activity times of introduced ship rats (Rattus rattus) on the same islands. The mongoose is implicated in a shift in rat activity times, but it is difficult to separate mongoose impacts on small mammal abundance from rat impacts. To manage introduced carnivores, we can exclude, control, or eradicate them. I review literature data on mongoose eradication and control campaigns. I compiled a list of all islands with known mongoose populations and focused on assessing successes, failures, and challenges. The mongoose has been eradicated only on six very small islands. Management at low levels by various techniques has been attempted on many islands, with variable success. On almost all islands of introduction, the mongoose has no potential competitors of similar size. However, on three Adriatic islands where the mongoose was introduced, a similar-sized native carnivore, the stone marten (Martes foina), is present, while on one Adriatic island the small Indian mongoose is the sole carnivore. To see if character displacement occurs in the mongoose when the marten is present, and vice-versa, I examined size variation in the diameter of the upper canine tooth (the prey-killing organ) and skull length in these two species on these islands. Character displacement in both traits was evident for the mongoose but not the marten. Lastly, I developed a simulation model to examine genetic consequences of serial introductions of the small Indian mongoose and found that the potential for population genetic data to determine introduction pathways and sequences is limited.

Chez les plantes à fleurs, la gynodioécie -- système dans lequel coexistent des individus femelles et des individus hermaphrodites -- est le système de reproduction le plus commun après l'hermaphrodisme. La question de l'évolution et surtout du maintien de la gynodioécie et du polymorphisme génétique sous-jacent a intrigué les chercheurs depuis le 19e siecle. Aujourd'hui, les grands principes de son évolution sont posés mais beaucoup de zones d'ombres persistent. Durant ma thèse, j'ai exploré trois aspects de la gynodioécie en utilisant une approche expérimentale chez l'espèce Silene nutans et une approche théorique. Je me suis en premier lieu intéressée au déterminisme génétique de la gynodioécie grâce à la réalisation de croisements contrôlés qui m'ont permis de montrer que le déterminisme génétique du sexe était cytonucléaire, c'est à dire contrôlé par plusieurs gènes de stérilité mâle cytoplasmique (CMS) et plusieurs restaurateurs nucléaires de fertilité. En parallèle, j'ai porté une attention particulière aux plantes gynomonoïques -- celles où coexistent sur le même pied des fleurs pistillés (femelles) et des fleurs parfaites (hermaphrodites) -- fréquentes chez Silene nutans comme chez d'autres espèces gynodioïques. J'ai montré que les caractéristiques reproductrices et florales de ce troisième phénotype sexuel étaient souvent intermédiaires entre celles des femelles et des hermaphrodites mais pouvaient dépendre de la proportion de fleurs pistillées sur la plante. Par ailleurs et contrairement à ce qui avait été suggéré, la plasticité du phénotype gynomonoïque s'est révélée être relativement réduite, suggérant un déterminisme génétique dont la caractérisation est encore en cours. La troisième partie de ma thèse a été motivée par les preuves récentes d'hétéroplasmie -- coexistence de différents génomes mitochondriaux au sein d'un individu -- et de la transmission occasionnelle du génome mitochondrial par le pollen chez Silene vulgaris. J'ai montré théoriquement que la présence d'un gène de stérilité mâle cytoplasmique favorisait l'évolution de la fuite paternelle de mitochondries. J'ai également vérifié expérimentalement l'hérédité mitochondriale chez Silene nutans par le génotypage des descendances de croisements contrôlés. / In flowering plants, gynodioecy -- a system in which females and hermaphrodites coexist within populations -- is the most common sexual system after hermaphroditism. The evolution and maintenance of gynodiocy and its underlying polymorphism have puzzled evolutionary biologists since the 19th century. The main principles of its evolution are well known but some points remain vague. During my PhD, I explored three aspects of gynodioecy using an experimental approach in the species Silene nutans and a theoretical approach. First, I studied the genetic determination of gynodioecy using controlled crosses that showed that the genetic determination of sex was cytonuclear, i.e. controlled by several cytoplasmic male sterility (CMS) genes and several nuclear restorers of fertility. Second, I focused on gynomonoecious plants -- those that carry both pistillate (female) flowers and perfect (hermaphrodite) flowers -- that are frequently found in Silene nutans as in other gynodioecious species. I showed that the floral and reproductive traits of this third sex phenotype were often intermediate between those of females and hermaphrodites but varied with varying proportions of pistillate flowers on the plant. Contrary to what was previously thought, the plasticity of the gynomoneocious phenotype was found to be limited, suggesting a genetic determination whose characterization is still in progress. The third part of my PhD was motivated by recent evidences of heteroplasmy -- the coexistence of different mitochondrial genomes within an individual -- and occasional transmission of the mitochondrial genome through pollen in Silene vulgaris. I showed theoretically that the occurrence of a cytoplasmic male sterility gene can favor the evolution of paternal leakage of mitochondria. I also investigated mitochondrial inheritance in Silene nutans by genotyping progenies from controlled crosses.

Every individual is born with different natural competencies that can be honed by both voluntary and involuntary environmental stimuli. The response our genotype decides to make, if any, towards those stimuli, determines how well our competencies develop. Each person’s coding and variations of genes will result in unique qualities in their phenotype, or physical structure. As a result, a person has various traits that are displayed through their behavior. DNA is genetically shown to express itself through traits by up to 75%. This leaves a sort of buffer of around 25%. This region is available for us to adapt to our environmental stimuli. Your innate qualities will not reach their full potential without stimulation from the environment, in a leadership case, with education and training and therefore it can be argued that environmental exposure is necessary to fully expose the potentials and capabilities of an individual, rather than instill a new skill or develop a talent that was not existent before. Innate leadership is not a permanent state, on the contrary, it is a continuously adaptive situation demanding contextual evolutionary changes or resignation from the subject occupying the role. When the needs and demands of a society or era outweigh the relevance of the innate leaders' traits and competencies, an evolution of leadership is needed to maintain a positive relationship between all parties involved. As a result, the innate leader will begin to lose their innateness in their role and unless they evolve and adapt (because the two actions are not the same) to new contextual needs, their tenure as leader will begin to be detrimental and counter-functional. What we want to put forward is a real, universal and constructive understanding of what makes a human happy, motivated and productive and how an innate person in context is a much better solution in the short and long run, for those around them when put to a task.