The genus Aneides (Caudata: Plethodontidae) is an arboreal salamander with a prehensile tail and a distribution that spans North America. It is hypothesized that adaptations for arboreality will be visible in the osteology of the sacral vertebra either by qualitative analysis or linear and morphometric analysis in comparison with other plethodontid salamanders. This study demonstrates that while qualitative and quantitative analyses are successful at making genus-level distinctions between taxa, identification to lower taxonomic levels remains inconclusive. Linear morphometrics and dorsal Procrustes landmarks were the most successful metrics to identify known taxa. Two unidentified fossil salamander sacral vertebrae from Oregon Caves National Monument are examined with the same techniques and are tentatively identified as Hydromantes based on qualitative similarities to modern Hydromantes specimens, as the quantitative analyses were unable to confidently diagnose the unknown specimens.

Understanding why some species coexist and others do not remains one of the fundamental challenges of ecology. While several lines of evidence suggest that closely related species are unlikely to occupy the same habitat because of competitive exclusion, there are many cases where closely related species do co-occur. Research comparing sympatric and allopatric populations of co-occurring species provides a framework to understand the role of phenotypic diversification in species coexistence. In this study I focus on the livebearing fish Poeciliopsis baenschi and ask if differences in phenotypic traits among populations can be explained by the presence or absence of the congeneric species P. turneri. I focus on phenotypic divergence in life history traits and in body shape, two sets of integrated traits likely to respond to variation in competition. Additionally, I compare explore the effects of sympatry and allopatry on sexual dimorphism. I take advantage of a natural experiment in western Mexico where P. baenschi co-occur with P. turneri in some locations (sympatric populations) but also exist in isolation in other locations (allopatric populations). My results show that sympatric populations of P. baenschi differed significantly in life history traits and body shape when compared to their allopatric counterparts. Additionally, the amount of sexual dimorphism differed between sympatric and allopatric populations of P. baenschi, suggesting different constraints might exist in sympatry and allopatry for sexual dimorphism. Lastly, I explore my results in the context of trait evolution as it relates to species coexistence.

Island isolation can cause changes in body size, cranial characteristics, and genetic variation in mammals. We use geometric morphometrics to test skull and mandible shape and size change across three species of endemic Cozumel Island rodents in order to test the “island rule” of larger size in isolated rodents. We also sequenced the D-Loop and cytochrome b region of the mitochondrial genome and tested for differences in genetic variation between island and mainland groups, as well as population structure and gene flow in order to assess the effect of island isolation on these three rodents. We found that the three species of rodents showed varying degrees of size and shape differences from island to mainland with some species varying considerably and others not at all. The genetic results were similar with some species exhibiting potential founder effects, while others showed little differentiation between the island and mainland. We conclude that evolution on islands is highly conditional on the history, community composition, and biology of the colonizing species.

In ancestry estimation of South African individuals, non-metric morphological trait assessment has not proven useful and previous results in FORDISC 3.0 leave room for improvement. The accuracy rates of software programs FORDISC 3.1 and 3D-ID were compared for ancestry estimation based on cranial data of black and white South Africans using discriminant function analysis. Cranial landmarks were digitized using a Microscribe G2 for geometric morphometric analysis in 3D-ID, and traditional craniometric measurements for use in FORDISC were calculated using the data collection software 3Skull. Data was collected from a total of 385 individuals (186 black and 199 white crania) from the Pretoria Bone Collection. Overall accuracy rates of 75.6% using FORDISC 3.1 and 63.1% using 3D-ID were obtained for black and white South Africans. Incorrect estimates were more often due to misclassifications of sex rather than ancestry, reflecting the decreased amount of sexual dimorphism in South African populations when compared against American populations, discussed previously. Black South Africans were more often classified correctly in FORDISC 3.1, and white South Africans were more often classified correctly in 3D-ID. Low sample size in comparative databases and broad ancestral differences between South Africans and the proxy populations used (American, European, and African) likely explain the low accuracy rates. The use of FORDISC and 3D-ID in conjunction can help South African anthropologists in estimating ancestry and ensuring correct classifications.

京都大学 / 新制・課程博士 / 博士(理学) / 甲第24181号 / 理博第4872号 / 新制||理||1697(附属図書館) / 京都大学大学院理学研究科生物科学専攻 / (主査)教授 中務 真人, 教授 森 哲, 准教授 森本 直記 / 学位規則第4条第1項該当 / Doctor of Science / Kyoto University / DFAM

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Select freshwater mussels in the genera Fusconaia, Pleurobema, and Pleuronaia were collected primarily in the upper Tennessee River basin from 2012 to 2014 for phylogenetic and morphological assessments. Freshwater mussels in these genera are similar in appearance, hence the need for phylogenetic verification and morphological assessment. Phylogenetic analyses of the mitochondrial gene ND1 and the nuclear gene ITS1 revealed three unrecognized, phylogenetically distinct species. These species were separated from their closest congener by 2.85%, 3.17%, and 6.32% based on pairwise genetic distances of ND1. Gaps created from aligning ITS1 sequences were coded as fifth characters, which phylogenetically separated most closely related species. Analyses of ND1 agreed with previous literature on the phylogenetic distinctiveness of Pleuronaia species, with the exception of the DNA sequences of P. gibberum, which grouped outside this genus based on the analyses conducted in this study. Morphological variation was recorded for eight of the species to include quantitative and qualitative characters as well as geometric morphometric analyses. Three decision trees were created from quantitative and qualitative characters using classification and regression tree analyses. The best-performing tree used quantitative and qualitative characters describing shell-only scenarios and obtained 80.6% correct classification on terminal nodes. Canonical variates analysis on geometric morphometric shell data revealed large morphological overlap between species. Goodall's F-tests between pairs of species revealed significant differences (a=0.05) between all but one species pairs; however, examination of landmarks on shells concluded large overlap of landmarks between species pairs. Lack of morphologically distinct characters to readily identify these phylogenetically distinct species indicates large morphological overlap among these species. Biologists need to be cognizant that morphologically cryptic species may exist in systems often explored. Three dichotomous keys were created from classification trees to identify select individuals in the genera Fusconaia, Pleurobema, and Pleuronaia; two of these keys, one for shells and one for live mussels were tested by participants with varying mussel identification skills to represent novices and experts. Both keys used continuous (quantitative) and categorical variables to guide participants to identifications. Novices, who had no prior mussel identification experience, correctly identified mussels with a 50% accuracy using the shell key and with a 51% accuracy using the live key. Experts, who had at least three years of experience identifying mussels, correctly identified mussels with a 58% accuracy using the shell key and with a 68% accuracy using the live key; however one expert noted that they did not use the live key to correctly identify one mussel. Morphological overlap of variables between mussels likely resulted in failure to consistently identify mussels correctly. Important management decisions and project implementations require accurate assessment of species' localities and populations. Incorrect species identification could hinder species' recovery efforts or prevent projects that otherwise could have continued if species are misidentified. If a mussel collection is thought to be a new record or could affect a project, I recommend that molecular genetic identifications be used to verify the species identity. / Master of Science

Thesis (MSc (Botany and Zoology))--Unkiversity of Stellenbosch, 2009. / Phylogeographic genetic structure has been documented for a number of southern African terrestrial taxa. Information regarding geographic population genetic structuring in multiple taxa, with differing life histories, can provide insights into abiotic processes such as vicariance. A fragment of the cytochrome b mitochondrial DNA gene of a plains-dwelling species, Otomys unisulcatus, was sequenced and analysed. Two closely related geographic assemblages were found. The first assemblage (lowland group) contains populations from both the eastern and western parts of the species range, and the second comprises populations from the Little Karoo (central group). The lowland group was shown to be in a state of population expansion after a relatively recent mitochondrial DNA (mtDNA) coalescence, while the genetic signature of the central assemblage was characterized by more genetic diversity indicative of an older lineage/genetic refuge. Areas of higher elevation (namely mountain ranges) appeared to be the main factor limiting gene flow between these two groups. Aridification cycles due to glacial maximum periods probably resulted in increased dispersal leading to the widespread distribution of common haplotypes throughout the lowland group. Morphological variation in skull shape and size has been shown to follow environmental clines in some rodents. Geometric morphometric analyses on the ventral and dorsal views of the craniums of O. unisulcatus were utilised to test whether the population groupings obtained in the genetic analyses would be recovered by morphometric analyses. In addition, it was also investigated which of the environmental factors investigated influenced skull shape and size. The genetic groupings were not recovered for either the cranial shape or size. Size variation in the females correlated positively with annual rainfall, and so by proxy with habitat productivity, indicating that females which inhabited areas with lower rainfall would be larger. The significant relationship between females’ centroid sizes and rainfall was thought to be as a result of the increased nutrient requirement by this gender in the production of offspring. The males did not show a significant correlation between any of the environmental variables and centroid size. There was a significant difference between the skull shapes of the genders, further verifying the sexual dimorphism in the species. Three major clusters were found (according to cranium shape) using a Two-Block Partial Least Squares Analysis (2B-PLS), which relate to the biome boundaries within the species’ range. Variations in shape were attributed to the varying needs for strong masticatory muscles resulting from differing diets. The skull shapes of specimens occurring along the escarpment were intermediate between the first two clusters. Cranial shape in the male dorsal view dataset was significantly correlated with the environmental variables block, possibly due to the much lower minimum temperature in the Sutherland population (a population which was not included in the female analyses). It was concluded that differing diets of individuals in the respective biomes influenced the shape of the cranium of both genders. The sexual dimorphism in the cranium shapes may be as a result of the females digging tunnels (using their teeth) underneath the stick nests. Otomys unisulcatus show high levels of phenotypic plasticity throughout the range and it thus appears that the species can adapt fast to the different environmental variables.