Pimelodella Eigenmann & Eigenmann, 1888 é um dos gêneros mais especiosos pertencentes à família Heptapteridae, com 71 espécies distribuídas desde o sul da América do Sul até o Panamá e América Central. A compreensão das relações filogenéticas desse grupo é ainda bastante confusa devido a dificuldades na identificação das espécies por suas semelhanças morfológicas, além da sua ampla diversidade e distribuição. Para melhor entendermos as relações existentes entre as espécies pertencentes a este gênero, nosso trabalho utilizou abordagens moleculares e morfológicas e foi organizado em quatro capítulos. No primeiro é apresentada uma breve revisão da bibliografia relacionada à Pimelodella, a área de estudo e as ferramentas que foram utilizadas para tentarmos compreender as relações filogenéticas e biogeográficas das espécies pertencentes ao gênero. Assim, para respondermos às questões propostas, no segundo capítulo avaliamos o potencial do método do código de barras do DNA para auxiliar na identificação das espécies, combinado com a análise de alguns caracteres morfológicos diagnósticos. Essas metodologias se mostraram muito úteis e eficazes, e nossos resultados indicam que é possível identificar grande parte das espécies com as metodologias escolhidas. O terceiro capítulo teve como objetivo estabelecer, as relações filogenéticas entre as espécies de Pimelodella incluídas nesse estudo, utilizando para tanto quatro genes mitocondriais (ATPase 6 e 8, citocromo b, COI e ND2). Através da análise de parcimônia foram obtidas seis árvores mais parcimoniosas. Os valores de suporte foram maiores nos nós mais internos. No quarto capítulo, apresentamos uma análise genético-populacional baseada em cinco loci de microssatélites na espécie troglóbia das cavernas da região do PETAR (Parque Estadual Turístico do Alto Ribeira). Os loci amplificados apresentaram altos níveis de polimorfismo e o número de alelos por loci variou de 9 no loco PC58 a 34 no locos PC87, o número médio de alelos por locus foi de 21,2. A estimativa global de FST, considerando-se todas as populações e todos os loci, foi significativamente diferente de zero (FST = 0,1353) sugerindo a ocorrência de diferenciação populacional na amostra. / Pimelodella Eigenmann & Eigenmann, 1888 is one of the most specious genus of the Siluriform family Heptapteridae, with 71 species distributed from southern South America to Panamá and Central America. The understanding of phylogenetic relationships within the genus is somewhat confusing due to the difficulties in morphological identification and its broad distribution. In order to assess the problems with species identification and phylogenetic relationships our work employed morphological and molecular tools is it is organized in four chapters. The first chapter contains an introduction to the problems and a revision of what its known in Pimelodella, as well as a brief description of the tools used. The second chapter deals with species identification and its subdivided into: morphology and the used of DNA barcoding. The results obtained with the combination of these two methodologies indicated, for example, that Pimelodella gracilis might comprise more than one species. The third chapter presents a phylogenetic analysis of the species included in this work based on nucleotide sequences of the mitochondrial genome. The parsimony analysis recovered six most parsimonious trees as expected the support values are larger towards the deeper nodes. The fourth chapter presents an population analysis based on five microsatellite loci to investigate whether or not the troglobitic species P. kronei displays population structuring in the caves of the PETAR (Parque Estadual Turístico do Alto Ribeira). The loci presented high polymorphism, the number of alleles raged from 9 in the locus PC58 to 34 in the locus PC87, the mean number of alleles per loci was 21,2. All loci showed private alleles PC17 and PC58 had 3 alleles and PC90 showed 22 private alleles distributed among all sampling locales. The global FST, estimative was significantly different from zero (FST = 0,1353) suggesting population.

Nannotrigona testaceicornis é uma espécie de abelha sem ferrão sendo que seus ninhos são largamente encontrados na zona urbana. Os meliponíneos estão entre os principais polinizadores da flora brasileira, no entanto, muitas espécies estão seriamente ameaçadas de extinção em consequência da perda do habitat e isolamento causados principalmente pelo desmatamento, uso indiscriminado de defensivos agrícolas e grandes queimadas, pois tais alterações resultam em ecossistemas fragmentados, formando mosaicos de vegetação remanescente, mergulhados numa paisagem antropizada. Nesse processo, grandes populações são reduzidas e subdivididas, o que pode acarretar alterações ecológicas e genéticas. Estudos populacionais de espécies de meliponíneos ainda são muito escassos, fazendo-se necessário a ampliação desses estudos para uma melhor compreensão da dinâmica populacional dessas abelhas. Neste contexto, este trabalho teve como objetivo a realização de um estudo populacional em ninhos amostrados nos estados de São Paulo e Minas Gerais, utilizando-se o mtDNA como ferramenta molecular. As análises através de PCR+RFLP de 05 regiões do mtDNA não revelaram polimorfismos nas populações estudadas, sendo detectado apenas um haplótipo. O estudo através do sequenciamento de um fragmento do gene COI I de sessenta operárias provenientes do campus da USPRP, Ribeirão Preto, Bonfim Paulista, Franca, Campinas, São Paulo, Uberlândia, Várzea da Palma, Viçosa e Caratinga, revelou a presença de cinco haplótipos nas populações amostradas dos quais três eram exclusivos de uma única populaçaõ e um era compartilhado por 70% das populações. A média da diversidade haplotípica (Hd= 0,264), e a diversidade nucleotídica (=0,00386) foram avaliadas revelando uma baixa divergência entre os haplótipos encontrados. As análises estatísticas revelaram que as populações estudadas estão estruturadas em três grupos, sendo esta estruturação um reflexo de eventos antigos em consequência de mudanças climáticas devido às glaciações do Pleistoceno levando a um gargalo populacional e posterior dispersão, juntamente com a barreira geográfica do mosaico de montanhas do complexo da Serra do Espinhaço que isolou duas das populações estudadas (Viçosa e Caratinga) levando à diferenciação das mesmas. / Nannotrigona testaceicornis is a stingless bee species whose nests are widely found in urban regions. The meliponines are among the most important Brazilian flora pollinators, however, many species are in seriously extinction danger due to habitat loss and isolation caused by deforestation, indiscriminate use of agricultural defensives, and great extent burnings. These changes result in fragmented ecosystems, in small extent of land showing residual vegetation, and in a human impacted landscape. In this process, large populations are reduced and subdivided, leading to ecological and genetic changes. Population studies of meliponine species are still scarce, showing the necessity of more investigation to a better understanding of the population dynamics of these bees. In this context, this work aimed to perform a population study in nests sampled in São Paulo and Minas Gerais states, using the mtDNA as a molecular tool. The PCR+RFLP analyses of five mtDNA regions did not show polymorphisms among the studied populations, and just one haplotype was detected. The study through CO I gene fragment sequencing in sixty workers collected in ten different places from the two Brazilian states mentioned above revealed the presence of five haplotypes. Three of them were exclusive to just one population and one was shared by 70% of the studied populations. The average haplotype diversity (Hd= 0.264) and the average nucleotide diversity (=0.00386) were estimated and showed low deviation among the haplotypes. The statistical analyses revealed that the studied populations are structured in three groups. This split may be explained as a consequence of ancient events caused by climatic changes due to Pleistocene glaciations resulting in a population bottleneck and later dispersion; in addition to these, a geographical barrier formed by the Serra do Espinhaço mountain complex, had isolated two of the studied populations (Viçosa and Caratinga), conducing them to differentiation.

Espécies de medusozoários com ciclos de vida muito diferentes habitam distintos mares e oceanos ao redor do mundo. Em uma escala regional, algumas espécies de hidrozoários estão amplamente distribuídas no Atlântico Sul-ocidental, (litorais do Brasil e Argentina), com populações habitando ambientes heterogêneos e estruturados. A relação entre a distribuição das espécies e a maior parte dos fatores ambientais é pouco conhecida. Deste modo, o objetivo de nosso estudo é pesquisar os padrões de distribuição e a estrutura genética populacional de duas espécies de hidrozoários do Atlântico Sul-ocidental em relação a: (1) as diferentes histórias naturais e (2) as distintas estruturas de massas d\'água do ambiente marinho. As espécies estudadas foram Olindias sambaquiensis (meroplanctônica, ciclo de vida: ovo ⊲ plânula ⊲ pólipo ⊲ medusa ⊲ ovo) e Liriope tetraphylla (holoplanctônica, ciclo de vida: ovo ⊲ plânula ⊲ medusa ⊲ ovo). Dados sobre a ecologia e história natural de tais espécies foram coletados e análises filogeográficas foram conduzidas utilizando os marcadores mitocondriais 16S e CO1. Nossos resultados revelaram um padrão filogeográfico similar para ambas as espécies. As populações brasileiras são basais e têm uma maior diversidade nucleotídica que as populações argentinas, as quais ocupam uma posição apical. O Rio da Prata não é uma barreira efetiva e introgressão possivelmente ocorre em ambas as espécies, podendo estar relacionada à circulação das massas d\'água. A estrutura genética encontrada para Olindias sambaquiensis pode estar relacionada com seu hábito demersal e afinidade com massas d\'água costeiras, e para Liriope tetraphylla com seu ciclo reprodutivo e auto-recrutamento. / Medusozoan species, with quite different life-cycles, inhabit different seas and oceans around the world. In a regional scale, some hydrozoan species are widespread along the Southwestern Atlantic Ocean (Brazilian and Argentinean shores), with populations distributed along a heterogeneous and structured environment. The relation between the distribution of the species and most of the biological and environmental factors is still largely unknown. Therefore, the aim of this study is to investigate the distributional patterns and genetic structure of populations of two hydrozoan species of SW Atlantic Ocean in relation to: (1) the different life histories and (2) the water masses structures of the marine environment. The species studied were the meroplanktonic Olindias sambaquiensis (life cycle: egg ⊲ planula ⊲ polyp ⊲ medusa ⊲ egg) and the holoplanktonic Liriope tetraphylla (life cycle: egg ⊲ planula ⊲ medusa ⊲ egg). We gathered data on the ecology and natural history of the species, and carried out phylogeographic analyses using CO1 and 16S DNA markers. Our results have shown similar phylogeographical patterns and genetic structures for both species. The Brazilian populations are basal and have a higher nucleotidic diversity than the apical Argentinean populations. The Rio de La Plata river is not an effective barrier, and introgression possibly occurs for both species and might be related to the circulation of the water masses. Biologically, the genetic structure found for Olindias sambaquiensis must be related to its demersal habit and close affinity to coastal water masses, and that found for Liriope tetraphylla must be related to its reproductive cycle and auto-recruitment.

The phylogenetics of eight species of the Peromyscus truei and P. boylii species groups from 15 populations were analyzed based on mitochondrial DNA sequence differentiation, using 13 hexanucleotide specific restriction enzymes. P. difficilis, P. nasutus, and P. attwateri were found to be members of the same clade. P. leucopus was not found to be closely related to any of the species of the boylii or truei species groups. Phylogenetic interpretations for the remaining species differed based on Wagner and Dollo parsimony analyses. P. true appears to be most closely related to P. gratus based on Wagner parsimony and the phenetic analysis, while the relationship of P. gratus to other species could not be resolved based on Dollo parsimony.

Abstract Neurological features are common in mitochondrial diseases because tissues depending upon oxidative phosphorylation bear the brunt of the pathogenesis. The 3243A>G mutation in the MTTL1 gene in mitochondrial DNA is regarded as the most frequent mitchondrial point mutation and classically presents with mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS). Myopathy and peripheral neuropathy have been documented in patients with mitochondrial diseases, but not properly characterised in patients with the 3243A>G mutation. We have previously determined the prevalence of patients with this mutation in a defined population in northern Finland. The clinical spectrum and molecular aspects of myopathy and peripheral neuropathy are analysed here in a population-based cohort of patients with 3243A>G. Fifty patients were examined neurologically in order to define the frequency of myopathy and its histological, ultrastructural and clinical features. The frequency and phenotypic variability of peripheral neuropathy were determined in 32 patients and muscle computed tomography findings recorded in 24 patients. Finally, variations in mutation heteroplasmy were analysed in 10 patients using single muscle fibre PCR analysis. The frequency of peripheral neuropathy was 22% (95% confidence interval (CI), 9–40%) and that of clinical myopathy 50% (95% CI, 36–64%). Moderate limb weakness was the most common myopathic feature, but mild weakness and external ophthalmoplegia were also present. CT scans revealed myopathic changes in 54% of the patients (95% CI, 33–76%), most frequently in the pelvic muscles. The incidence of myopathy was highest in the fifth decade of life, and higher age and male gender increased the risk of neuropathy. Muscle histology was abnormal in 72% of the cases examined (95% CI, 55–86%). The presence of intramitochondrial crystals and COX-negative fibres and variations in the size and shape of mitochondria were more common in the muscle of myopathic patients. Single muscle fibre analysis pointed to a correlation between the mutation load in ragged red fibres and in adjacent histologically normal fibres, and the proportion of 3243A>G in histologically normal muscle fibres showed a pattern compatible with random genetic drift. The results indicate that myopathy and peripheral neuropathy are common in patients with the 3243A>G and that myopathy is highly variable in presentation. Segregation of 3243A>G in individual muscle fibres showed a complex process with random and non-random elements.

Abstract Mitochondrial DNA (mtDNA) is a maternally inherited 16.6 kbp circular genome that codes for 13 subunits of the mitochondrial respiratory chain, 2 rRNAs and 22 tRNAs. The mutation rate in mtDNA is high and therefore, mutations have accumulated sequentially to lineages that have diverged tens of thousands of years ago. The neutral theory predicts that a proportion of these variations may be slightly deleterious, associated with diseases and selected against, but the issue is still controversial. This study reports an analysis of selection against mutations in mtDNA. First, the population prevalence of one of the most pathogenic mtDNA mutations, the common MELAS mutation (3243A>G), was determined in a population-based screening setting in Northern Ostrobothnia, and the reproductive capacity, or genetic fitness, of women with the mutation was estimated in order to measure for the first time the degree of host-level selection against this highly pathogenic mutation. The frequency of 3243A>G was high, as the minimum estimate for the prevalence was 10.2/100,000, and this together with the geographical distribution of maternal ancestors of the mutation carriers suggested that nuclear genes may be involved in the population history of the mutation. Surprisingly, the genetic fitness of mutation carriers was not reduced, suggesting that the average host-level selection against carriers is not strong. Second, all available complete human mtDNA sequences worldwide (N=847) were collected into a database and analysed for evidence to support the hypothesis concerning slightly deleterious mutations and selective constraints imposed by lineage-specific interactions. 465 distinct missense and 6 nonsense mutations were identified. 48% of the amino acid replacements changed the polarity, 44% hydropathy, 32% aliphaticity, 26% size, 13% aromaticity, and 8% charge. Nonconservative amino acid replacements were found to be more common among the evolutionarily recent mutations than among the older ones, and mutations that have arisen more than once during human evolution showed different properties from the remaining ones. The major continent-specific mtDNA lineages were analysed in terms of nucleotide diversity indices, neutrality tests and nonsynonymous/synonymous rate ratios, and patterns suggesting selective constraints possibly due to lineage-specific interactions were identified. Moreover, a general correlation between nucleotide position and nucleotide polymorphism was identified in the mtDNA. The results are compatible with the assumption that selection has a marked role in human mtDNA evolution and that selective constraints may vary between populations, so that the pathogenic potential of a given mutation may depend markedly on the presence of other, interacting mutations.

Abstract The 3243A>G mutation in mitochondrial DNA (mtDNA), the most common cause of the syndrome of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes, is also associated with many other phenotypes such as hearing loss, diabetes mellitus, epilepsy, cognitive decline, myopathy and cardiomyopathy. The prevalence of the mutation has been shown to be 16.3/100 000 adults in Northern Finland. The present study was performed to estimate the frequency and progression of cardiac abnormalities and to examine causes of death in patients with 3243A>G. Left ventricular hypertrophy (LVH) was found in echocardiography in 56% of patients with 3243A>G and in 15% of age and sex-matched controls. The median thickness of the diastolic interventricular septum or posterior wall was 14 mm in the patients with LVH. The prevalence of LVH determined by echocardiography increased from 40% to 56% in 25 patients with 3243A>G during three years of follow-up, this trend being especially marked among the diabetic patients. The ultra-low-frequency (ULF) and very-low-frequency (VLF) components of the spectral analysis of heart rate variability (HRV) were lower among the patients with 3243A>G than in matched controls (p = 0.02 in ULF and p = 0.04 in VLF), and the short-term fractal scaling exponent in detrended fluctuation analysis of HRV was lower in the patients with 3243A>G (1.16 ± 0.18 vs. 1.28 ± 0.13) (p < 0.01). Survival analysis of a birth cohort from pedigrees with 3243A>G revealed excess mortality before the age of 50 years. Neurological and cardiovascular diseases accounted for 32% of all the underlying causes of death in families with 3243A>G. Death was sudden and unexpected in 31% of cases in which 3243A>G was considered to be involved in the cause of death. The results show that cardiac abnormalities are frequent and progressive in patients with the 3243A>G mtDNA mutation and that cardiac autonomic regulation is disturbed. Patients with the 3243A>G mutation and their first degree maternal relatives died younger than was presupposed by their life expectancy at birth or at 15 years. The most common causes of death were neuropsychiatric and cardiovascular diseases.

Eastern part of the African Sahel, connecting sub-Saharan Africa with North and East Africa, play an important role as a bidirectional corridor for vertically and horizontally migrations of populations. It is the strategic region to study human genetic diversity due to the presence of ethnically, linguistically, culturally and geographically diversity. This work is focused on the analysis of HVS-I and HVS-II segments of mtDNA. The work provides new information about genetic structure and migration activity of this region by analysis twelve populations belonging to three African linguistic families and different subsistent strategies. Analysis of mtDNA revealed the higher diversity of the populations of east Sudan and Horn of Africa, which is connected with the spreading of populations along the Nile River. It seems, that in this region linguistic factors have bigger impact on genetic diversity then the geografic ones. The opposite situation is observed in populations of Chad, where populations with similiar geografic location and different linguistic affilation revealed low genetic differentiation. The intra-population analysis shows the significant influence of genetic drift on the pastoralists living on the Red Sea Coast - Beja and Rashaida. In Beja is probably due to decrease of size of...

>Magister Scientiae - MSc / The primary objective of this Masters project was to investigate the maternal ancient substructure of the Griqua population in South Africa. Genetic ancestry was determined by investigating ancestry informative single nucleotide polymorphisms. These are located in the control region of the mitochondrial genome. The auxiliary aim was to test the validity of the UWC 10plex system in relation to a sample group of Griqua males. This short tandem repeat multiplex targets specific mutations confined to paternal lineages. The Khoi Khoi or Hottentots were the first inhabitants in the Cape. Indigenous Khoi Khoi female slaves had offspring with the European settlers in the 1800s which resulted in the Griqua population group. The incorporated European paternal ancestry is what set the Griqua apart from the native population groups at that time. Colonisation events from the mid-17th to 19th Century and the apartheid regime resulted in land dispossession of the native population and an extensively mixed gene pool in South Africa. One hundred and seventy six (N=176) male and female Griqua people were collectively sampled in Kokstad (2012), Vredendal (2012 and 2013) and at the Griqua National Conference in Ratelgat (2013). All 176 samples were analysed using mtDNA control region Sanger sequencing. The sample group (N=176) was separated based on birthplace (Origin sample group and post-colonial sample group). The origin sample group consists of individuals whose ancestors were not part of the Griqua Trek to Northern regions of South Africa and were less likely to be exposed to colonial influences. Mutations within the hypervariable segments of the mtDNA control region were used to infer haplogroups with geographic-specific population data. In this way one can plot the extent of ancient Khoisan (L0d) and Bantu influences (L1-L5) as well as the influence of East (M, A, B, E) and West (N, R, J, H) Eurasian haplogroups in the maternal ancestry of the Griqua population group. The origin sample group showed 91% African ancestry (76.8% L0d) while the post-colonial group had 78% African ancestry (60% L0d). The origin sample group had 2% East Eurasian and 7% West Eurasian ancestry, while the post-colonial group contained 20% Eurasian ancestry. There is greater admixture in the post-colonial group which can be attributed to the integration of surrounding populations during settlement periods in parts of the Northern Cape and KwaZulu-Natal. The UWC 10plex STR kit was tested to see if it could discriminate between male individuals of this admixed sample group (N=91 males). The markers for this multiplex were selected according to their ability to differentiate between individuals of African descent. It proved to be a viable Y chromosome short tandem repeat testing tool, displaying a statistically significant discrimination capacity value of 0.966 and only having 3 shared haplotypes in the sample group of 91 Griqua males. / National Research Foundation (NRF)

Biogeographers have long searched for common processes responsible for driving diversification in the Holarctic region. Although terrestrial flora and fauna have been well studied, much of the marine biogeographic work addresses patterns and processes occurring over a relatively recent timescale. A prerequisite to comparative biogeographic analysis requires well-resolved phylogenies of similarly distributed taxa that diverged over a similar timeframe. The overall aim of my Ph.D. thesis was to address fundamental questions in the systematics and biogeography of a family of Holarctic fish (Osmeridae) and place these results in a broad comparative biogeographic framework. With eight conflicting morphological hypotheses, the northern hemisphere smelts have long been the subjects of systematic disagreement. In addition to the uncertainty in the interrelationships within this family, the relationship of the Osmeridae to several other families remains unclear. Using DNA sequence data from three mitochondrial and three nuclear genes from multiple individuals per species, I reconstructed the phylogenetic relationships among the 6 genera and 15 osmerid species. Phylogenetic reconstruction and divergence dating yielded a well-resolved phylogeny of the osmerid genera and revealed several interesting evolutionary patterns within the family: (1) Hypomesus chishimaensis and H. nipponensis individuals are not reciprocally monophyletic, suggesting that they are conspecific and H. chishimaensis is a recently evolved freshwater ecotype that invaded the Kuril Islands following the last glaciation, (2) The trans-Pacific sister relationships in Hypomesus based on lateral line scale counts are not supported, implying that this phenotype evolved in parallel on each side of the North Pacific Ocean, (3) The Plecoglossidae are the Osmeridae sister group, (4) Over half of the characters from previous studies show evidence of parallel evolution; however, 27 traits reflect ancestral relationships, (5) Multiple divergences within the Osmeridae date to both the mid-Miocene cooling period and the Pliocene Bering Seaway opening, suggesting these events were important in the evolution of these fishes, and (6) Divergences in many marine taxa for which dated phylogenies are available are also correlated with these time periods. Future research should target additional Holarctic marine taxa for further comparative analysis. / Science, Faculty of / Zoology, Department of / Graduate