Šio darbo metu naudojant 5 mikrosatelitinius DNR žymenis buvo bandoma išsiaiškinti, ar į Lietuvą natūraliai atplaukiantys upiniai unguriai skiriasi nuo į Lietuvą introdukuotų upinių ungurių genetiškai. Vietines Anguilla anguilla populiacijas atstovavo Baltijos jūros ir Kuršių marių imtys, o introdukuotas – Dringio ir Siesarčio ežerų imtys. Tikrinama buvo, tiek izoliacijos dėl atstumo (IBD), tiek laikinės izoliacijos (IBT), įtaka A. anguilla genetinei diferenciacijai. Nors genetinė diferenciacija tarp didžiosios dalies lyginamų imčių buvo maža (FST = 0,0042) ir nepatikima (p > 0,05), tačiau remdamiesi gautais tyrimo rezultatais negalime patvirtinti panmiksinės hipotezės A. anguilla rūšyje, kadangi mažos (FST = 0,0143) ir patikimos (p = 0,0018) genetinės diferenciacijos nustatymas tarp Siesarčio ežero introdukuotų upinių ungurių leidžia teigti, kad genetinė diferenciacija Anguilla anguilla rūšyje egzistuoja. / In order to find out whether native and introduced Anguilla anguilla populations differ one from another genetically I have used 5 microsatellite markers and compared 2 native between 2 introduced European eel samples. Native A. anguilla samples were taken from Baltic sea and Curonian lagoon, while introduced samples were taken from Dringis and Siesartis lakes. During this work I tried to find out not only IBD, but also IBT impact to A. anguilla genetic differentiation. Experiment results do not reject panmixia hypothesis in European eel, because there are small (FST = 0,0042) and not significant (p > 0,05) genetic differentiation among all samples used in this experiment. However, there is no enough data to say that A. anguilla genetic differentiation does not exist at all, because there is small (FST = 0,0143) and significant (p = 0,0018) genetic differentiation among lake Siesartis samples.

Broad whitefish, Coregonus nasus, is an important subsistence fish species in Arctic North America, yet virtually nothing is known regarding the genetic population structure of Nearctic populations of this species. In this thesis, microsatellite DNA variation was assayed among 1213 broad whitefish from 47 localities throughout North America, with emphasis on the Mackenzie River system, Northwest Territories. Specifically, I examined geographic variation in allele frequencies to assess how historical factors (Pleistocene glaciations) have shaped the current structuring of genetic variability and population differentiation. Microsatellite data was also used to resolve the relative contributions of broad whitefish populations to subsistence fisheries in the Mackenzie River system. Overall, broad whitefish exhibit relatively high intrapopulation microsatellite variation (average 12.29 alleles/locus, average HE = 0.58) and there were declines in these measures of genetic diversity with distance from putative refugia suggesting historical factors, namely post-glacial dispersal, have influenced current microsatellite variation. Interpopulation divergence was low (overall FST = 0.07), but the main regions assayed in this study (Russia, Alaska, Mackenzie River and Travaillant Lake systems) are genetically differentiated. Strong isolation-by-distance among samples was resolved when including only those populations occupying former Beringia, but not when assaying those at the periphery of the range in the Mackenzie River system, suggesting that broad whitefish in the Mackenzie system have not occupied the region long enough since their invasion post-glacially to have approached equilibrium between gene flow and drift. Mixture analysis indicated that most fish from the lower Mackenzie River subsistence fishery originated from the Peel River, highlighting the importance of this tributary. Additionally the mixture analysis provides evidence for a putative riverine life history form in the Mackenzie River. My results indicate that glaciation and post-glacial colonization have been important in shaping the current genetic population structure of North American broad whitefish. They also illustrate the utility of microsatellite DNA to delineate population structure and patterns of genetic diversity in recently founded populations in addition to resolving contributions to fisheries. My data also support the hypothesis that there are several designatable units of conservation among broad whitefish populations and that management strategies should be implemented accordingly.

Broad whitefish, Coregonus nasus, is an important subsistence fish species in Arctic North America, yet virtually nothing is known regarding the genetic population structure of Nearctic populations of this species. In this thesis, microsatellite DNA variation was assayed among 1213 broad whitefish from 47 localities throughout North America, with emphasis on the Mackenzie River system, Northwest Territories. Specifically, I examined geographic variation in allele frequencies to assess how historical factors (Pleistocene glaciations) have shaped the current structuring of genetic variability and population differentiation. Microsatellite data was also used to resolve the relative contributions of broad whitefish populations to subsistence fisheries in the Mackenzie River system. Overall, broad whitefish exhibit relatively high intrapopulation microsatellite variation (average 12.29 alleles/locus, average HE = 0.58) and there were declines in these measures of genetic diversity with distance from putative refugia suggesting historical factors, namely post-glacial dispersal, have influenced current microsatellite variation. Interpopulation divergence was low (overall FST = 0.07), but the main regions assayed in this study (Russia, Alaska, Mackenzie River and Travaillant Lake systems) are genetically differentiated. Strong isolation-by-distance among samples was resolved when including only those populations occupying former Beringia, but not when assaying those at the periphery of the range in the Mackenzie River system, suggesting that broad whitefish in the Mackenzie system have not occupied the region long enough since their invasion post-glacially to have approached equilibrium between gene flow and drift. Mixture analysis indicated that most fish from the lower Mackenzie River subsistence fishery originated from the Peel River, highlighting the importance of this tributary. Additionally the mixture analysis provides evidence for a putative riverine life history form in the Mackenzie River. My results indicate that glaciation and post-glacial colonization have been important in shaping the current genetic population structure of North American broad whitefish. They also illustrate the utility of microsatellite DNA to delineate population structure and patterns of genetic diversity in recently founded populations in addition to resolving contributions to fisheries. My data also support the hypothesis that there are several designatable units of conservation among broad whitefish populations and that management strategies should be implemented accordingly. / Science, Faculty of / Zoology, Department of / Graduate

The communal breeding system of the smooth-billed ani (Crotophaga ani) was studied at two wildlife refuges in southwest Puerto Rico. Groups ranged in size from 2 to 9 adults, and communal clutches ranged in size from 11 to more than 25 eggs. Microsatellite DNA loci were isolated and used to examine the mating system and the extent of reproductive skew in individual groups. Loci were also screened in guira cuckoos (Guira guira) to examine the relationships suggested by Quinn et al. (1994). In the four focal smooth-billed ani groups, I found suggestions of monogamy, polygamy, and incidents of intraspecific brood parasitism. In all groups, incubated clutch size and microsatellite data indicate that subordinate females are gaining some reproductive success. At one nest, evidence suggested a decrease in the intensity of reproductive skew between successive nests. Although the data are limited, they suggest that alternative strategies to monogamy may be more prevalent than previously believed, and that reproductive skew may be affected by the availability of limiting resources within the breeding season. / Thesis / Master of Science (MS)

I examined the population genetic structure of three known subspecies of Glaucomys sabrinus from Appalachia, Washington State, and two previously unexamined populations from Mount Rogers National Recreation Area (MRNRA) in Southwestern Virginia. Mean FST (0.107) and an AMOVA (P G. sabrinus subspecies populations in the southern Appalachians are genetically differentiated. Glaucomys sabrinus at MRNRA were less inbred than expected. Gene flow, a consensus tree based on Nei's genetic distance, elevated heterozygosity and morphometric data suggest that the MRNRA G. sabrinus population is an intergrade of the two recognized Appalachian subspecies, G. s. fuscus and G. s. coloratus. I compared inbreeding and the level of parasite infestation in the two MRNRA populations of G. sabrinus and found that Whitetop Mountain (150 ha habitat) was more inbred than the population on Mount Rogers (400 ha habitat, P Strongyloides robustus were greater in the more fragmented Whitetop Mountain population, although the difference was not statistically significant (P= 0.278). A Mantel comparison of genetic diversity and parasite infestation among individuals did show a highly significant negative correlation (P G. sabrinus form a unique insular population with high genetic diversity that is nonetheless susceptible to increased inbreeding, and elevated parasitism caused by fragmentation. MRNRA G. sabrinus should retain endangered species status.

As abelhas da tribo Euglossini, possuem elevada representatividade nas florestas tropicais (25% da comunidade apícola existente) distribuindo-se do sul dos EUA ao centro da Argentina, sendo restritas à região Neotropical. A espécie Euglossa pleosticta, com ocorrência relatada exclusivamente no território brasileiro, possui hábito de vida solitário e costuma estar presente em levantamentos realizados em remanescentes da Mata Atlântica. Pouco se sabe sobre sua estrutura populacional e os efeitos da fragmentação florestal sobre as mesmas. Sendo assim, a realização de um estudo populacional para esta espécie é algo relevante, uma vez que colabora para a compreensão dos efeitos da fragmentação florestal na variabilidade genética do grupo, sendo objetivo deste trabalho, caracterizar a variabilidade genética e morfológica desta espécie, utilizando ferramentas morfológicas (Morfometria Geométrica de asas e Assimetria Flutuante), e moleculares (DNA microssatélite e DNA mitocondriais). Sendo assim, trabalhamos com 293 amostras de E. pleosticta coletadas em três fragmentos de mata no Estado de São Paulo. Para as análises morfológicas, foram marcados 18 marcos anatômicos nas intersecções das nervuras das asas anterior direita de cada abelha. Nas análises de microssatélite, trabalhamos com oito loci heterólogos e para realizarmos as análises de DNA mitocondrial, analisamos 20 abelhas por localidade, amplificando segmentos do Citocromo B. Nas análises de Morfometria Geométrica e Microssatélites de DNA, as localidades estudadas formaram dois grupos, os quais corroboraram quanto às características de fitofisionomia, clima, altitude e distância geográfica compartilhadas entre as localidades. Nossos dados sugerem a presença de ecotipos localmente adaptados, o que pode ser explicado em função da plasticidade fenotípica, a qual é muito comum em insetos que vivem em ambientes variados. Na análise de Assimetria Flutuante, observamos valores significativos de assimetria flutuante e assimetria direcional para as três localidades estudadas. Já na análise de DNA mitocondrial, encontramos nove haplótipos, com diversidade nucleotídica (? = 0,01636) e diversidade haplotípica (Hd = 0,777), sendo apenas um destes haplótipos compartilhado (H2). O teste de Fst par a par indicou estruturação genética populacional, e na AMOVA a maior taxa de variação observada foi quando consideramos a estruturação de um único grupo com variação interpopulacional (61,9%). Os testes de Mantel realizados tanto para distância genética quanto para distância morfológica, não apresentaram correlação quando relacionadas com distância geográfica. A falta de concordância entre os marcadores moleculares, é algo que já foi relatado em outros trabalhos e pode ser explicado em função da diferente taxa de evolução dos mesmos, uma vez que o marcador mitocondrial é mais conservado quando comparado com o de microssatélite. Em conjunto, estes marcadores apontam para a formação de subpopulações localmente adaptadas (ecotipos) para a espécie de E. pleosticta, provavelmente em decorrência dos processos recentes de fragmentação de habitat. / The bees from Euglossini tribe have high representativeness in tropical forests (25% of existing bee community) and are distributed from the south of USA to the center of Argentina, being restricted to Neotropical region. The Euglossa pleosticta species, with occurrence reported exclusively in the Brazilian territory, has solitary behaviour and, according to some researches, use to be present in Atlantic forest remnants. Little is known about its population structure and the forest fragments effects over them. Therefore, the realization of a population study of this species is relevant, since it contributes to the comprehension of the forest fragmentation effects in the genetic variability of this group. The ultimate goal of this research was to characterize the genetic and morphological variability of this species, usinging morphological tools (Geometric Morphometrics of forewings and Fluctuation Asymmetry) and molecular tools (Microsatellite DNA and Mitocondrial DNA). Thus, we have worked with 293 samples of E. pleosticta, which were collected from three forest fragments in São Paulo state. For the morphological analyses, 18 landmarks were plotted in the vein intersections of the right forewing of each bee. On the Microsatellite DNA analysis, we have worked with eight heterologous loci and on the Mitocondrial DNA analysis, we amplified the Cytochrome B segments to 20 bees per locality. In the Geometric Morphometry and DNA Microsatellites analyzes, two groups were formed from the studied localities, which corroborated to the characteristics of phytophysiognomy, climate, altitude and geographic distance shared between the localities. Our data suggest the presence of locally adapted ecotypes, which can be explained by phenotypic plasticity, which is very common in insects living in different environments. In the Fluctuation Asymmetry analysis, we observed significant values of Fluctuation and Directional Asymmetry for all studied localities. In the mitochondrial DNA analysis, we found nine haplotypes with nucleotide diversity (? = 0.01636) and haplotypic diversity (Hd = 0.777), where only one was shared (H2). The Fst pairwise test indicated population genetic structuring and, in AMOVA, the highest rate of variation was observed when we considered the structuring of a single group with interpopulation variation (61.9%). The Mantel test performed for both genetic and morphological distances, did not present correlation when related to geographic distance. The disagreement between the molecular markers has already been reported in other studies and can be explained by the different rate of evolution of these markers, since the mitochondrial marker is more conserved when compared to the microsatellite. Together, these markers indicate the formation of locally adapted subpopulations (ecotypes) for the species E. pleosticta, probably due to the recent cases of habitat fragmentation.

As abelhas da tribo Euglossini, possuem elevada representatividade nas florestas tropicais (25% da comunidade apícola existente) distribuindo-se do sul dos EUA ao centro da Argentina, sendo restritas à região Neotropical. A espécie Euglossa pleosticta, com ocorrência relatada exclusivamente no território brasileiro, possui hábito de vida solitário e costuma estar presente em levantamentos realizados em remanescentes da Mata Atlântica. Pouco se sabe sobre sua estrutura populacional e os efeitos da fragmentação florestal sobre as mesmas. Sendo assim, a realização de um estudo populacional para esta espécie é algo relevante, uma vez que colabora para a compreensão dos efeitos da fragmentação florestal na variabilidade genética do grupo, sendo objetivo deste trabalho, caracterizar a variabilidade genética e morfológica desta espécie, utilizando ferramentas morfológicas (Morfometria Geométrica de asas e Assimetria Flutuante), e moleculares (DNA microssatélite e DNA mitocondriais). Sendo assim, trabalhamos com 293 amostras de E. pleosticta coletadas em três fragmentos de mata no Estado de São Paulo. Para as análises morfológicas, foram marcados 18 marcos anatômicos nas intersecções das nervuras das asas anterior direita de cada abelha. Nas análises de microssatélite, trabalhamos com oito loci heterólogos e para realizarmos as análises de DNA mitocondrial, analisamos 20 abelhas por localidade, amplificando segmentos do Citocromo B. Nas análises de Morfometria Geométrica e Microssatélites de DNA, as localidades estudadas formaram dois grupos, os quais corroboraram quanto às características de fitofisionomia, clima, altitude e distância geográfica compartilhadas entre as localidades. Nossos dados sugerem a presença de ecotipos localmente adaptados, o que pode ser explicado em função da plasticidade fenotípica, a qual é muito comum em insetos que vivem em ambientes variados. Na análise de Assimetria Flutuante, observamos valores significativos de assimetria flutuante e assimetria direcional para as três localidades estudadas. Já na análise de DNA mitocondrial, encontramos nove haplótipos, com diversidade nucleotídica (? = 0,01636) e diversidade haplotípica (Hd = 0,777), sendo apenas um destes haplótipos compartilhado (H2). O teste de Fst par a par indicou estruturação genética populacional, e na AMOVA a maior taxa de variação observada foi quando consideramos a estruturação de um único grupo com variação interpopulacional (61,9%). Os testes de Mantel realizados tanto para distância genética quanto para distância morfológica, não apresentaram correlação quando relacionadas com distância geográfica. A falta de concordância entre os marcadores moleculares, é algo que já foi relatado em outros trabalhos e pode ser explicado em função da diferente taxa de evolução dos mesmos, uma vez que o marcador mitocondrial é mais conservado quando comparado com o de microssatélite. Em conjunto, estes marcadores apontam para a formação de subpopulações localmente adaptadas (ecotipos) para a espécie de E. pleosticta, provavelmente em decorrência dos processos recentes de fragmentação de habitat. / The bees from Euglossini tribe have high representativeness in tropical forests (25% of existing bee community) and are distributed from the south of USA to the center of Argentina, being restricted to Neotropical region. The Euglossa pleosticta species, with occurrence reported exclusively in the Brazilian territory, has solitary behaviour and, according to some researches, use to be present in Atlantic forest remnants. Little is known about its population structure and the forest fragments effects over them. Therefore, the realization of a population study of this species is relevant, since it contributes to the comprehension of the forest fragmentation effects in the genetic variability of this group. The ultimate goal of this research was to characterize the genetic and morphological variability of this species, usinging morphological tools (Geometric Morphometrics of forewings and Fluctuation Asymmetry) and molecular tools (Microsatellite DNA and Mitocondrial DNA). Thus, we have worked with 293 samples of E. pleosticta, which were collected from three forest fragments in São Paulo state. For the morphological analyses, 18 landmarks were plotted in the vein intersections of the right forewing of each bee. On the Microsatellite DNA analysis, we have worked with eight heterologous loci and on the Mitocondrial DNA analysis, we amplified the Cytochrome B segments to 20 bees per locality. In the Geometric Morphometry and DNA Microsatellites analyzes, two groups were formed from the studied localities, which corroborated to the characteristics of phytophysiognomy, climate, altitude and geographic distance shared between the localities. Our data suggest the presence of locally adapted ecotypes, which can be explained by phenotypic plasticity, which is very common in insects living in different environments. In the Fluctuation Asymmetry analysis, we observed significant values of Fluctuation and Directional Asymmetry for all studied localities. In the mitochondrial DNA analysis, we found nine haplotypes with nucleotide diversity (? = 0.01636) and haplotypic diversity (Hd = 0.777), where only one was shared (H2). The Fst pairwise test indicated population genetic structuring and, in AMOVA, the highest rate of variation was observed when we considered the structuring of a single group with interpopulation variation (61.9%). The Mantel test performed for both genetic and morphological distances, did not present correlation when related to geographic distance. The disagreement between the molecular markers has already been reported in other studies and can be explained by the different rate of evolution of these markers, since the mitochondrial marker is more conserved when compared to the microsatellite. Together, these markers indicate the formation of locally adapted subpopulations (ecotypes) for the species E. pleosticta, probably due to the recent cases of habitat fragmentation.

Microsatellites are repetitive DNA characterized by tandem repeats of short motifs (2 – 5 bp). High mutation rates make them ideal for population level studies. Microsatellite allele genesis is generally attributed to strand slippage, and it is assumed that alleles are caused only by changes in repeat number. Most analyses are limited to alleles (electromorphs) scored by mobility only, and models of evolution rarely account for homoplasy in allele length. Additionally, insertion/deletion events (indels) in the flanking region or interruptions in the repeat can obfuscate the accuracy of genotyping. Many investigators use microsatellites, designed for a focal species, to screen for genetic variation in non-focal species. Comparative studies have shown different mutation rates of microsatellites in different species, and even individuals. Recent studies have used reciprocal comparisons to assess the level of polymorphism of microsatellites between pairs of taxa. In this study, I investigated the evolution of microsatellites within a phylogenetic context, using comparisons within the rodent family Bathyergidae. Bathyergidae represents a monophyletic group endemic to sub-Saharan Africa and relationships are well supported by morphological and molecular data. Using mitochondrial and nuclear DNA, a robust phylogeny was generated for the Bathyergidae. From my results, I proposed the new genus, Coetomys. I designed species-specific genotyping and microsatellite flanking sequence (MFS) primers for each genus. Sequencing of the MFS provided direct evidence of the evolutionary dynamics of the repeat motifs and their flanking sequence, including rampant electromorphic homoplasy, null alleles, and indels. This adds to the growing body of evidence regarding problems with genotype scores from fragment analysis. A number of the loci isolated were linked with repetitive elements (LTRs and SINEs), characterized as robust phylogenetic characters. Results suggest that cryptic variation in microsatellite loci are not trivial and should be assessed in all studies. The phylogenetic utility of the nucleotide variation of the MFS was compared to the well-resolved relationships of this family based on the 12S/TTR phylogeny. Variation observed in MFS generated robust phylogenies, congruent with results from 12S/TTR. Finally, a number of the indels within the MFS provided a suite of suitable phylogenetic characters.

Understanding the events and processes responsible for patterns of within species diversity, provides insight into major evolutionary themes like adaptation, species distributions, and ultimately speciation itself. Here, I combine ecological, genetic and spatial perspectives to evaluate the roles that both historical and contemporary factors have played in shaping the population structure and genetic variation of foxsnakes (Pantherophis gloydi). First, I determine the likely impact of habitat loss on population distribution, through radio-telemetry (32 individuals) at two locations varying in habitat patch size. As predicted, individuals had similar habitat use patterns, but restricted movements to patches of suitable habitat at the more disturbed site. Also, occurrence records spread across a fragmented region were non-randomly distributed and located close to patches of usable habitat, suggesting habitat distribution limits population distribution. Next, I combined habitat suitability modeling with population genetics (589 individuals, 12 microsatellite loci) to infer how foxsnakes disperse through a mosaic of natural and altered landscape features. Boundary regions between genetic clusters were comprised of low suitability habitat (e.g. agricultural fields). Island populations were grouped into a single genetic cluster suggesting open water presents less of a barrier than non-suitable terrestrial habitat. Isolation by distance models had a stronger correlation with genetic data when including resistance values derived from habitat suitability maps, suggesting habitat degradation limits dispersal for foxsnakes. At larger temporal and spatial scales I quantified patterns of genetic diversity and population structure using mitochondrial (101 cytochrome b sequences) and microsatellite (816 individuals, 12 loci) DNA and used Approximate Bayesian computation to test competing models of demographic history. Supporting my predictions, I found models with populations which have undergone population size drops and splitting events continually had more support than models with small founding populations expanding to stable populations. Based on timing, the most likely cause was the cooling of temperatures and infilling of deciduous forest since the Hypisthermal. On a smaller scale, evidence suggested anthropogenic habitat loss has caused further decline and fragmentation. Mitochondrial DNA structure did not correspond to fragmented populations and the majority of foxsnakes had an identical haplotype, suggesting a past bottleneck or selective sweep. / Thesis (Ph.D, Biology) -- Queen's University, 2011-01-11 10:40:52.476

Bumble bees (Bombus spp.) are adept pollinators of countless cultivated and wild flowering plants, but many species have experienced declines in recent decades. Though urban sprawl has been implicated as a driving force of such losses, urban green spaces hold the potential to serve as habitat islands for bumble bees. As human populations continue to grow and metropolitan areas become larger, the survival of many bumble bee species will hinge on the identification and implementation of appropriate conservation measures at regional and finer scales. North Texas is home to some the fastest-growing urban areas in the country, including Denton County, as well as at least two declining bumble bee species (B. pensylvanicus and B. fraternus). Using a combination of field , molevular DNA and GIS methods I evaluated the persistence of historic bumble bee species in Denton County, and investigated the genetic structure and connectivity of the populations in these spaces. Field sampling resulted in the discovery of both B. pensylvanicus and B. fraternus in Denton County's urban green spaces. While the relative abundance of B. fraternus in these spaces was significantly lower than historic levels gleaned from museum recors, that of B. pensylvanicus was significantly higher. Statistical analyses found that both bare ground and tree cover surrounding sample sites were negatively associated with numbers of bumble bee individuals and hives detected in these green spaces. Additionally, limited genetic structuring of bumble bee populations was detected, leading to the conclusion that extensive gene flow is occurring across populations in Denton County.