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<title>Francis X. Villablanca</title>
<copyright>Copyright (c) 2012  All rights reserved.</copyright>
<link>http://works.bepress.com/fvillabl</link>
<description>Recent documents in Francis X. Villablanca</description>
<language>en-us</language>
<lastBuildDate>Sat, 24 Nov 2012 04:37:41 PST</lastBuildDate>
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<title>Consequences of a Genetic Bottleneck in California Condors: A Mitochondrial DNA Perspective</title>
<link>http://works.bepress.com/fvillabl/9</link>
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<pubDate>Fri, 18 Nov 2011 14:48:47 PST</pubDate>
<description>
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	<p>The California Condor (<em>Gymnogyps californianus</em>) 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.</p>

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<author>Mary S. Adams et al.</author>


<category>Articles</category>

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<title>Spatial and Temporal Continuity of Kangaroo Rat Populations Shown by Sequencing Mitochondrial DNA from Museum Specimens</title>
<link>http://works.bepress.com/fvillabl/8</link>
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<pubDate>Mon, 14 Nov 2011 10:42:09 PST</pubDate>
<description>
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	<p>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 rat<em>Dipodomys panamintinus</em> 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.</p>

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<author>W. Kelley Thomas et al.</author>


<category>Contributions to Books</category>

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<title>Invasion genetics of the Mediterranean fruit fly: variation in multiple nuclear introns</title>
<link>http://works.bepress.com/fvillabl/7</link>
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<pubDate>Mon, 14 Nov 2011 10:42:07 PST</pubDate>
<description>
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	<p>Biological invasions generally start from low initial population sizes, leading to reduced genetic variation in nuclear and especially mitochondrial DNA. Consequently, genetic approaches for the study of invasion history and population structure are difficult. An extreme example is the Mediterranean fruit fly, Ceratitis capitata (Medfly), for which successive invasions during this century have resulted in a loss of 60% of ancestral genetic variation in isozymes and 75% of variation in mitochondrial DNA. Using Medflies as an example, we present a new approach to invasion genetics that measures DNA sequence variation within introns from multiple nuclear loci. These loci are so variable that even relatively recently founded Medfly populations within California and Hawaii retain ample genetic diversity. Invading populations have only lost 35% of the ancestral genetic variation. Intron variation will allow high-resolution genetic characterization of invading populations in both natural and managed systems, although non-equilibrium methods of analysis may be necessary if the genetic diversity represents sorting ancestral polymorphism.</p>

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</description>

<author>F. X. Villablanca et al.</author>


<category>Articles</category>

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<title>Invasion genetics of New World medflies: testing alternative colonization scenarios</title>
<link>http://works.bepress.com/fvillabl/6</link>
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<pubDate>Mon, 14 Nov 2011 10:42:06 PST</pubDate>
<description>
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	<p>The Mediterranean fruit fly (<em>Ceratitis capitata</em>) is an invasive  agricultural pest with a wide host range and a nearly global  distribution. Efforts to forgo the medfly''s 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 (<em>F</em> <sub>ST</sub>) 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 (<em>N</em> <sub>e</sub> = 5 × 10<sup>2</sup> individuals per population), small invasions from a single source consistently produced <em>F</em> <sub>ST</sub> 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 (<em>N</em> <sub>e</sub> 5 × 10<sup>3</sup>).  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.</p>

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</description>

<author>Andrew J. Bohonak et al.</author>


<category>Articles</category>

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<title>Dynamics of mitochondrial DNA evolution in animals: Amplification and sequencing with conserved primers</title>
<link>http://works.bepress.com/fvillabl/5</link>
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<pubDate>Mon, 14 Nov 2011 10:42:04 PST</pubDate>
<description>
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	<p>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.</p>

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</description>

<author>T. D. Kocher et al.</author>


<category>Conference Proceedings</category>

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<title>Disparate Rates of Molecular Evolution in Cospeciating Hosts and Parasites</title>
<link>http://works.bepress.com/fvillabl/4</link>
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<pubDate>Mon, 14 Nov 2011 10:42:02 PST</pubDate>
<description>
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	<p>DNA sequences for the gene encoding mitochondrial cytochrome oxidase I  in a group of rodents (pocket gophers) and their ectoparasites                         (chewing lice) provide evidence for cospeciation  and reveal different rates of molecular evolution in the hosts and  their                         parasites. The overall rate of nucleotide  substitution (both silent and replacement changes) is approximately  three times                         higher in lice, and the rate of synonymous  substitution (based on analysis of fourfold degenerate sites) is  approximately                         an order of magnitude greater in lice. The  difference in synonymous substitution rate between lice and gophers  correlates                         with a difference of similar magnitude in  generation times.</p>

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</description>

<author>M. S. Hafner et al.</author>


<category>Articles</category>

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<title>Low genetic diversity in an endangered species: recent or historic pattern?</title>
<link>http://works.bepress.com/fvillabl/3</link>
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<pubDate>Mon, 14 Nov 2011 10:42:01 PST</pubDate>
<description>
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	<p>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.</p>

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</description>

<author>Marjorie D. Matocq et al.</author>


<category>Articles</category>

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<title>Is population genetics mired in the past?</title>
<link>http://works.bepress.com/fvillabl/2</link>
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<pubDate>Mon, 14 Nov 2011 10:41:59 PST</pubDate>
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<author>Andrew J. Bohonak et al.</author>


<category>Articles</category>

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<title>Spatial and Temporal Aspects of Populations Revealed by Mitochondrial DNA</title>
<link>http://works.bepress.com/fvillabl/1</link>
<guid isPermaLink="true">http://works.bepress.com/fvillabl/1</guid>
<pubDate>Mon, 14 Nov 2011 10:41:58 PST</pubDate>
<description>
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	<p>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.</p>

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</description>

<author>Francis X. Villablanca</author>


<category>Articles</category>

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