Spatial and Temporal Aspects of Populations Revealed by Mitochondrial DNA

The evolutionary analysis of DNA sequences bridges phylogenetics and population genetics. Ancient DNA (aDNA) alJows the study of extinct genotypes, populations, and species, as well as dichronic comparisons of extant populations and species. Thus a DNA forges an empirical link between history and two inherently historical fields of research. Fortunately, the conceptual frameworks of phylogenetics and population genetics can easily be extended to encompass advances being made in the study of aDNA

Invasion genetics of New World medflies: testing alternative colonization scenarios

The Mediterranean fruit fly (Ceratitis capitata) is an invasive agricultural pest with a wide host range and a nearly global distribution. Efforts to forgo the medfly\u27\u27s spread into the United States are dependent on an understanding of population dynamics in newly established populations elsewhere. To explore the potential influence of demographic and historical parameters in six medfly populations distributed from Mexico to Peru, we created population genetic null models using Monte Carlo simulations. Null expectations for genetic differentiation (F ST) were compared with actual sequence variation from four highly polymorphic nuclear loci. Four colonization scenarios that were modeled led to unique genetic signatures that could be used to interpret empirical data. Unless current gene flow across Latin America was assumed to be very high, we could reject colonizations consisting of multiple introductions, each of low genetic diversity. Further, if simulated populations were small (N e = 5 × 102 individuals per population), small invasions from a single source consistently produced F ST values comparable to those currently observed in Latin America. In contrast, only large invasions from diverse sources were compatible with the observed data for large populations (N e 5 × 103). This study demonstrates that alternative population genetic hypotheses can be tested empirically even when departures from equilibrium are extreme, and that population genetic theory can be used to explore the processes that underlie biological invasions

Climactic Niche Model for Overwintering Monarch Butterflies in a Topographically Complex Region of California

We use climatic conditions that are associated with known monarch butterfly overwintering groves in California to build a Maxent model, and focus on the fine scale probability of overwintering grove occurrence in a topographically complex region of the state (Santa Barbara County). Grove locations are known from recent and historical surveys and a long-term citizen science database. The climatic niche model performs well, predicting that overwintering habitat is most likely to occur along the coast and at low elevations, as shown by empirical data. We then use climatic variables in conjunction with climate change scenarios to model the future location of overwintering habitat, and find a substantial shift in the predicted distribution. Under a plausible scenario, the probability of occurrence of overwintering habitat directly reflects elevation, with coastal regions having a reduced probability relative to today, and higher elevation sites increasing in probability. Under a more extreme scenario, high probability sites are only located along ridgelines and in mountaintop regions of the county. This predicted shift in distribution is likely to have management implications, as sites that currently lack monarchs may become critical to conservation in the future. Our results suggest that estimating the size of the western overwintering population in the future will be problematic, unless annual counts compensate for a shift in the distribution and a potential change in the number and location of occupied sites

Consequences of a Genetic Bottleneck in California Condors: A Mitochondrial DNA Perspective

The California Condor (Gymnogyps californianus) has recently survived a severe population bottleneck. The entire population was reduced to 27 individuals in 1982. The number of genetic founders was even smaller. We obtained 482 base pairs of DNA sequence from the mitochondrial control region (CR) of all founder individuals that potentially represented unique maternal haplotypes. Four unique haplotypes were present in the genetic founders. One of these haplotypes is unique to Topatopa, a male brought into captivity in 1967, whose haplotype will not persist in the future population. Haplotype diversity (h) was reduced by 25% between the founder population and our census of the 2002 population. Nucleotide diversity (θ) did not vary significantly between the founders and the current population. Our results provide insights into condor genetics. First, where recessive deleterious alleles have been expressed in progeny (e.g., chondrodystrophy) the breeding pair shares the same mitochondrial haplotype. Second, we identifi ed the presence of a nuclear copy of the mitochondrial control region and provide condor specific primer sequences to preferentially amplify DNA of mitochondrial origin. Third, we confirm low levels of genetic diversity in the captive population as suggested by previous research. Forth, we question whether the low level of diversity is a consequence of the 20th century bottleneck, or if diversity has been historically low over a much longer time scale

Low genetic diversity in an endangered species: recent or historic pattern?

Examining patterns of genetic diversity has become an integral component of many management plans concerning endangered species, yet interpreting the processes underlying such patterns remains challenging. We demonstrate low genetic diversity in a critically endangered small mammal population. A common interpretation of this pattern would be that it is the result of a known, recent decline in this population. We test this interpretation and find it to be incorrect. Instead, by using museum voucher specimens, we show that the pattern of low genetic diversity is historical. This study demonstrates the importance of choosing appropriate reference groups by which to interpret modern levels of genetic diversity in endangered species. We conclude that analysis of archival specimens may be essential in cases where genetic diversity is driving conservation management decisions because it may allow us to distinguish the effects of low genetic diversity from the process of losing diversity. We recognize that this approach can be limited due to several sampling issues: archival material may not be available, statistical power needs to be evaluated, sample sizes and sequence lengths may be suboptimal due to intrinsic difficulties associated with amplification of degraded DNA. These issues are discussed and possible solutions identified

Determining the source of individuals: multilocus genotyping in nonequilibrium population genetics

Recently founded populations represent an enormous challenge for genetic analysis: new populations are often genetically impoverished, making it hard to find sufficiently variable markers, and what little variation is present tends to be ancestral, rendering phylogenetic methods inappropriate. Recently, novel genetic markers and new statistical analyses have made multilocus genotyping an invaluable tool in the fledgling field of nonequilibrium population genetics. Such advances are not of mere academic interest but address questions of great economic, medical and conservation significance

Meiosis decreases recombination load; Mitosis increases recombination load

Chiasmata are necessary for proper chromosomal segregation, but can result in inadvertent recombination. Bernstein and Michod demonstrated that meiosis evolved as a means of error correction, not genetic mixing. Therefore meiotic recombination is not the sine qua non of sex, but is instead an epiphenomenon of imperfect meiotic error correction. By correcting against recombinant genotypes, meiosis reduces recombination load, thereby providing an unappreciated selective advantage for sex. Sex reducing recombination load should be integrated into population genetic models of multi-locus epistasis for maintenance of sex and may explain sequestration of germ lines in animals. We predict that eumetazoa have less recombination load than sexual organisms without a germ line. Mitosis largely lacks the error correction of meiosis, destroys linkage through ubiquitous mitotic recombination, and thereby increases recombination load, especially in co-adapted gene complexes. Meiosis and possibly karyogamy provide an unexpected benefit to sex, offsetting at least some of the famed costs of sex

Spatial and Temporal Continuity of Kangaroo Rat Populations Shown by Sequencing Mitochondrial DNA from Museum Specimens

The advent of direct sequencing via the polymerase chain reaction (PCR) has opened up the possibility of molecular studies on museum specimens. Here we analyze genetic variation in populations over time by applying PCR to DNA extracted from museum specimens sampled from populations of one species over the last 78 years. Included in this study were 43 museum specimens of the Panamint kangaroo ratDipodomys panamintinus from localities representing each of three geographically distinct subspecies. These specimens were originally collected and prepared as dried skins in 1911, 1917, or 1937. For each specimen, a 225-bp segment of the mitochondrial genome was sequenced. These mitochondrial DNA sequences were compared to those of 63 specimens collected at the same localities in 1988. The three subspecies were nearly completely distinct. Only 2 of the 106 individuals shared mitochondrial types between subspecies. For all three localities, the diversity levels were maintained between the two temporal samples. The concordance observed between the two temporally separate phylogenies supports the use of museum specimens for phylogenetic inference. This study demonstrates the accuracy and routine nature of the use of museum specimens in the analysis of mitochondrial sequence variation in natural populations and, importantly, that a temporal aspect can now be added to such studies

Dynamics of mitochondrial evolution in animals : amplification and sequencing with conserved primers

With a standard set of primers directed toward conserved regions, we have used the polymerase chain reaction to amplify homologous segments of mtDNA from more than 100 animal species, including mammals, birds, amphibians, fishes, and some invertebrates. Amplification and direct sequencing were possible using unpurified mtDNA from nanogram samples of fresh specimens and microgram amounts of tissues preserved for months in alcohol or decades in the dry state. The bird and fish sequences evolve with the same strong bias toward transitions that holds for mammals. However, because the light strand of birds is deficient in thymine, thymine to cytosine transitions are less common than in other taxa. Amino acid replacement in a segment of the cytochrome b gene is faster in mammals and birds than in fishes and the pattern of replacements fits the structural hypothesis for cytochrome b. The unexpectedly wide taxonomic utility of these primers offers opportunities for phylogenetic and population research