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        <title>BMC Evolutionary Biology - Most accessed articles</title>
        <link>http://www.biomedcentral.com/bmcevolbiol/</link>
        <description>The most accessed research articles published by BMC Evolutionary Biology</description>
        <dc:date>2009-12-04T00:00:00Z</dc:date>
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                                <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2148/9/266" />
                                <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2148/9/282" />
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                                <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2148/9/267" />
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        <item rdf:about="http://www.biomedcentral.com/1471-2148/9/266">
        <title>Phylogenomic analysis of the cystatin superfamily in eukaryotes and prokaryotes</title>
        <description>Background:
The cystatin superfamily comprises cysteine protease inhibitors that play key regulatory roles in protein degradation processes. Although they have been the subject of many studies, little is known about their genesis, evolution and functional diversification. Our aim has been to obtain a comprehensive insight into their origin, distribution, diversity, evolution and classification in Eukaryota, Bacteria and Archaea.
Results:
We have identified in silico the full complement of the cystatin superfamily in more than 2100 prokaryotic and eukaryotic genomes. The analysis of numerous eukaryotic genomes has provided strong evidence for the emergence of this superfamily in the ancestor of eukaryotes. The progenitor of this superfamily was most probably intracellular and lacked a signal peptide and disulfide bridges, much like the extant Giardia cystatin. A primordial gene duplication produced two ancestral eukaryotic lineages, cystatins and stefins. While stefins remain encoded by a single or a small number of genes throughout the eukaryotes, the cystatins have undergone a more complex and dynamic evolution through numerous gene and domain duplications. In the cystatin superfamily we discovered twenty vertebrate-specific and three angiosperm-specific orthologous families, indicating that functional diversification has occurred only in multicellular eukaryotes. In vertebrate orthologous families, the prevailing trends were loss of the ancestral inhibitory activity and acquisition of novel functions in innate immunity. Bacterial cystatins and stefins may be emergency inhibitors that enable survival of bacteria in the host, defending them from the host&apos;s proteolytic activity.
Conclusion:
This study challenges the current view on the classification, origin and evolution of the cystatin superfamily and provides valuable insights into their functional diversification. The findings of this comprehensive study provide guides for future structural and evolutionary studies of the cystatin superfamily as well as of other protease inhibitors and proteases.</description>
        <link>http://www.biomedcentral.com/1471-2148/9/266</link>
                <dc:creator>Dusan Kordis</dc:creator>
                <dc:creator>Vito Turk</dc:creator>
                <dc:source>BMC Evolutionary Biology 2009, 9:266</dc:source>
        <dc:date>2009-11-18T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-2148-9-266</dc:identifier>
        <prism:publicationName>BMC Evolutionary Biology</prism:publicationName>
        <prism:issn>1471-2148</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>266</prism:startingPage>
        <prism:publicationDate>2009-11-18T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedcentral.com/1471-2148/9/282">
        <title>Diversity, phylogenetic distribution, and origins of venomous catfishes</title>
        <description>Background:
The study of venomous fishes is in a state of relative infancy when compared to that of other groups of venomous organisms. Catfishes (Order Siluriformes) are a diverse group of bony fishes that have long been known to include venomous taxa, but the extent and phylogenetic distribution of this venomous species diversity has never been documented, while the nature of the venoms themselves also remains poorly understood. In this study, I used histological preparations from over 100 catfish genera, basic biochemical and toxicological analyses of fin spine extracts from several species, and previous systematic studies of catfishes to examine the distribution of venom glands in this group. These results also offer preliminary insights into the evolutionary history of venom glands in the Siluriformes.
Results:
Histological examinations of 158 catfish species indicate that approximately 1250-1625+ catfish species should be presumed to be venomous, when viewed in conjunction with several hypotheses of siluriform phylogeny. Maximum parsimony character optimization analyses indicate two to three independent derivations of venom glands within the Siluriformes. A number of putative toxic peptides were identified in the venoms of catfish species from many of the families determined to contain venomous representatives. These peptides elicit a wide array of physiological effects in other fishes, though any one species examined produced no more than three distinct putative toxins in its venom. The molecular weights and effects produced by these putative toxic peptides show strong similarities to previously characterized toxins found in catfish epidermal secretions.
Conclusion:
Venom glands have evolved multiple times in catfishes (Order Siluriformes), and venomous catfishes may outnumber the combined diversity of all other venomous vertebrates. The toxic peptides found in catfish venoms may be derived from epidermal secretions that have been demonstrated to accelerate the healing of wounds, rather than defensive crinotoxins.</description>
        <link>http://www.biomedcentral.com/1471-2148/9/282</link>
                <dc:creator>Jeremy Wright</dc:creator>
                <dc:source>BMC Evolutionary Biology 2009, 9:282</dc:source>
        <dc:date>2009-12-04T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-2148-9-282</dc:identifier>
        <prism:publicationName>BMC Evolutionary Biology</prism:publicationName>
        <prism:issn>1471-2148</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>282</prism:startingPage>
        <prism:publicationDate>2009-12-04T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.biomedcentral.com/1471-2148/7/214">
        <title>BEAST: Bayesian evolutionary analysis by sampling trees</title>
        <description>Background:
The evolutionary analysis of molecular sequence variation is a statistical enterprise. This is reflected in the increased use of probabilistic models for phylogenetic inference, multiple sequence alignment, and molecular population genetics. Here we present BEAST: a fast, flexible software architecture for Bayesian analysis of molecular sequences related by an evolutionary tree. A large number of popular stochastic models of sequence evolution are provided and tree-based models suitable for both within- and between-species sequence data are implemented.
Results:
BEAST version 1.4.6 consists of 81000 lines of Java source code, 779 classes and 81 packages. It provides models for DNA and protein sequence evolution, highly parametric coalescent analysis, relaxed clock phylogenetics, non-contemporaneous sequence data, statistical alignment and a wide range of options for prior distributions. BEAST source code is object-oriented, modular in design and freely available at http://beast-mcmc.googlecode.com/ under the GNU LGPL license.
Conclusion:
BEAST is a powerful and flexible evolutionary analysis package for molecular sequence variation. It also provides a resource for the further development of new models and statistical methods of evolutionary analysis.</description>
        <link>http://www.biomedcentral.com/1471-2148/7/214</link>
                <dc:creator>Alexei Drummond</dc:creator>
                <dc:creator>Andrew Rambaut</dc:creator>
                <dc:source>BMC Evolutionary Biology 2007, 7:214</dc:source>
        <dc:date>2007-11-08T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-2148-7-214</dc:identifier>
        <prism:publicationName>BMC Evolutionary Biology</prism:publicationName>
        <prism:issn>1471-2148</prism:issn>
        <prism:volume>7</prism:volume>
        <prism:startingPage>214</prism:startingPage>
        <prism:publicationDate>2007-11-08T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedcentral.com/1471-2148/9/268">
        <title>Convergent evolution, habitat shifts and variable diversification rates in the ovenbird-woodcreeper family (Furnariidae)</title>
        <description>Background:
The Neotropical ovenbird-woodcreeper family (Furnariidae) is an avian group characterized by exceptionally diverse ecomorphological adaptations. For instance, members of the family are known to construct nests of a remarkable variety. This offers a unique opportunity to examine whether changes in nest design, accompanied by expansions into new habitats, facilitates diversification. We present a multi-gene phylogeny and age estimates for the ovenbird-woodcreeper family and use these results to estimate the degree of convergent evolution in both phenotype and habitat utilisation. Furthermore, we discuss whether variation in species richness among ovenbird clades could be explained by differences in clade-specific diversification rates, and whether these rates differ among lineages with different nesting habits. In addition, the systematic positions of some enigmatic ovenbird taxa and the postulated monophyly of some species-rich genera are evaluated.
Results:
The phylogenetic results reveal new examples of convergent evolution and show that ovenbirds have independently colonized open habitats at least six times. The calculated age estimates suggest that the ovenbird-woodcreeper family started to diverge at ca 33 Mya, and that the timing of habitat shifts into open environments may be correlated with the aridification of South America during the last 15 My. The results also show that observed large differences in species richness among clades can be explained by a substantial variation in net diversification rates. The synallaxines, which generally are adapted to dry habitats and build exposed vegetative nests, had the highest diversification rate of all major furnariid clades.
Conclusion:
Several key features may have played an important role for the radiation and evolution of convergent phenotypes in the ovenbird-woodcreeper family. Our results suggest that changes in nest building strategy and adaptation to novel habitats may have played an important role in a diversification that included multiple radiations into more open and bushy environments. The synallaxines were found to have had a particularly high diversification rate, which may be explained by their ability to build exposed vegetative nests and thus to expand into a variety of novel habitats that emerged during a period of cooling and aridification in South America.</description>
        <link>http://www.biomedcentral.com/1471-2148/9/268</link>
                <dc:creator>Martin Irestedt</dc:creator>
                <dc:creator>Jon Fjeldsa</dc:creator>
                <dc:creator>Love Dalen</dc:creator>
                <dc:creator>Per Ericson</dc:creator>
                <dc:source>BMC Evolutionary Biology 2009, 9:268</dc:source>
        <dc:date>2009-11-21T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-2148-9-268</dc:identifier>
        <prism:publicationName>BMC Evolutionary Biology</prism:publicationName>
        <prism:issn>1471-2148</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>268</prism:startingPage>
        <prism:publicationDate>2009-11-21T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedcentral.com/1471-2148/7/219">
        <title>Yarrowia lipolytica vesicle-mediated protein transport pathways</title>
        <description>Background:
Protein secretion is a universal cellular process involving vesicles which bud and fuse between organelles to bring proteins to their final destination. Vesicle budding is mediated by protein coats; vesicle targeting and fusion depend on Rab GTPase, tethering factors and SNARE complexes. The G&#233;nolevures II sequencing project made available entire genome sequences of four hemiascomycetous yeasts, Yarrowia lipolytica, Debaryomyces hansenii, Kluyveromyces lactis and Candida glabrata. Y. lipolytica is a dimorphic yeast and has good capacities to secrete proteins. The translocation of nascent protein through the endoplasmic reticulum membrane was well studied in Y. lipolytica and is largely co-translational as in the mammalian protein secretion pathway.
Results:
We identified S. cerevisiae proteins involved in vesicular secretion and these protein sequences were used for the BLAST searches against G&#233;nolevures protein database (Y. lipolytica, C. glabrata, K. lactis and D. hansenii). These proteins are well conserved between these yeasts and Saccharomyces cerevisiae. We note several specificities of Y. lipolytica which may be related to its good protein secretion capacities and to its dimorphic aspect. An expansion of the Y. lipolytica Rab protein family was observed with autoBLAST and the Rab2- and Rab4-related members were identified with BLAST against NCBI protein database. An expansion of this family is also found in filamentous fungi and may reflect the greater complexity of the Y. lipolytica secretion pathway. The Rab4p-related protein may play a role in membrane recycling as rab4 deleted strain shows a modification of colony morphology, dimorphic transition and permeability. Similarly, we find three copies of the gene (SSO) encoding the plasma membrane SNARE protein. Quantification of the percentages of proteins with the greatest homology between S. cerevisiae, Y. lipolytica and animal homologues involved in vesicular transport shows that 40% of Y. lipolytica proteins are closer to animal ones, whereas they are only 13% in the case of S. cerevisiae.
Conclusion:
These results provide further support for the idea, previously noted about the endoplasmic reticulum translocation pathway, that Y. lipolytica is more representative of vesicular secretion of animals and other fungi than is S. cerevisiae.</description>
        <link>http://www.biomedcentral.com/1471-2148/7/219</link>
                <dc:creator>Dominique Swennen</dc:creator>
                <dc:creator>Jean-Marie Beckerich</dc:creator>
                <dc:source>BMC Evolutionary Biology 2007, 7:219</dc:source>
        <dc:date>2007-11-12T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-2148-7-219</dc:identifier>
        <prism:publicationName>BMC Evolutionary Biology</prism:publicationName>
        <prism:issn>1471-2148</prism:issn>
        <prism:volume>7</prism:volume>
        <prism:startingPage>219</prism:startingPage>
        <prism:publicationDate>2007-11-12T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedcentral.com/1471-2148/9/264">
        <title>Genome wide evolutionary analyses reveal serotype specific patterns of positive selection in selected Salmonella serotypes</title>
        <description>Background:
The bacterium Salmonella enterica includes a diversity of serotypes that cause disease in humans and different animal species. Some Salmonella serotypes show a broad host range, some are host restricted and exclusively associated with one particular host, and some are associated with one particular host species, but able to cause disease in other host species and are thus considered &quot;host adapted&quot;. Five Salmonella genome sequences, representing a broad host range serotype (Typhimurium), two host restricted serotypes (Typhi [two genomes] and Paratyphi) and one host adapted serotype (Choleraesuis) were used to identify core genome genes that show evidence for recombination and positive selection.
Results:
Overall, 3323 orthologous genes were identified in all 5 Salmonella genomes analyzed. Use of four different methods to assess homologous recombination identified 270 genes that showed evidence for recombination with at least one of these methods (false discovery rate [FDR] &lt;10%). After exclusion of genes with evidence for recombination, site and branch specific models identified 41 genes as showing evidence for positive selection (FDR &lt;20%), including a number of genes with confirmed or likely roles in virulence and ompC, a gene encoding an outer membrane protein, which has also been found to be under positive selection in other bacteria. A total of 8, 16, 7, and 5 genes showed evidence for positive selection in Choleraesuis, Typhi, Typhimurium, and Paratyphi branch analyses, respectively. Sequencing and evolutionary analyses of four genes in an additional 42 isolates representing 23 serotypes confirmed branch specific positive selection and recombination patterns.
Conclusion:
Our data show that, among the four serotypes analyzed, (i) less than 10% of Salmonella genes in the core genome show evidence for homologous recombination, (ii) a number of Salmonella genes are under positive selection, including genes that appear to contribute to virulence, and (iii) branch specific positive selection contributes to the evolution of host restricted Salmonella serotypes.</description>
        <link>http://www.biomedcentral.com/1471-2148/9/264</link>
                <dc:creator>Yesim Soyer</dc:creator>
                <dc:creator>Renato Orsi</dc:creator>
                <dc:creator>Lorraine Rodriguez-Rivera</dc:creator>
                <dc:creator>Qi Sun</dc:creator>
                <dc:creator>Martin Wiedmann</dc:creator>
                <dc:source>BMC Evolutionary Biology 2009, 9:264</dc:source>
        <dc:date>2009-11-14T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-2148-9-264</dc:identifier>
        <prism:publicationName>BMC Evolutionary Biology</prism:publicationName>
        <prism:issn>1471-2148</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>264</prism:startingPage>
        <prism:publicationDate>2009-11-14T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedcentral.com/1471-2148/9/267">
        <title>Diversification of the cullin family</title>
        <description>Background:
Cullins are proteins involved in ubiquitination through their participation in multisubunit ubiquitin ligase complexes. In this study, I use comparative genomic data to establish the pattern of emergence and diversification of cullins in eukaryotes.
Results:
The available data indicate that there were three cullin genes before the unikont/bikont split, which I have called Cul&#945;, Cul&#946; and Cul&#947;. Fungal species have quite strictly conserved these three ancestral genes, with only occasional lineage-specific duplications. On the contrary, several additional genes appeared in the animal or plant lineages. For example, the human genes Cul1, Cul2, Cul5, Cul7 and Parc all derive from the ancestral Cul&#945; gene. These results, together with the available functional data, suggest that three different types of ubiquitin ligase cullin-containing complexes were already present in early eukaryotic evolution: 1) SCF-like complexes with Cul&#945; proteins; 2) Cul&#946;/BTB complexes; and, 3) Complexes containing Cul&#947; and DDB1-like proteins. Complexes containing elongins have arisen more recently and perhaps twice independently in animals and fungi.
Conclusion:
Most of the known types of cullin-containing ubiquitin ligase complexes are ancient. The available data suggest that, since the origin of eukaryotes, complex diversity has been mostly generated by combining closely related subunits, while radical innovations, giving rise to novel types of complexes, have been scarce. However, several protist groups not examined so far contain highly divergent cullins, indicating that additional types of complexes may exist.</description>
        <link>http://www.biomedcentral.com/1471-2148/9/267</link>
                <dc:creator>Ignacio Marin</dc:creator>
                <dc:source>BMC Evolutionary Biology 2009, 9:267</dc:source>
        <dc:date>2009-11-19T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-2148-9-267</dc:identifier>
        <prism:publicationName>BMC Evolutionary Biology</prism:publicationName>
        <prism:issn>1471-2148</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>267</prism:startingPage>
        <prism:publicationDate>2009-11-19T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedcentral.com/1471-2148/9/283">
        <title>Phenotypic novelty in experimental hybrids is predicted by the genetic distance between species of cichlid fish</title>
        <description>Background:
Transgressive segregation describes the occurrence of novel phenotypes in hybrids with extreme trait values not observed in either parental species. A previously experimentally untested prediction is that the amount of transgression increases with the genetic distance between hybridizing species. This follows from QTL studies suggesting that transgression is most commonly due to complementary gene action or epistasis, which become more frequent at larger genetic distances. This is because the number of QTLs fixed for alleles with opposing signs in different species should increase with time since speciation provided that speciation is not driven by disruptive selection. We measured the amount of transgression occurring in hybrids of cichlid fish bred from species pairs with gradually increasing genetic distances and varying phenotypic similarity. Transgression in multi-trait shape phenotypes was quantified using landmark-based geometric morphometric methods.
Results:
We found that genetic distance explained 52% and 78% of the variation in transgression frequency in F1 and F2 hybrids, respectively. Confirming theoretical predictions, transgression when measured in F2 hybrids, increased linearly with genetic distance between hybridizing species. Phenotypic similarity of species on the other hand was not related to the amount of transgression.
Conclusions:
The commonness and ease with which novel phenotypes are produced in cichlid hybrids between unrelated species has important implications for the interaction of hybridization with adaptation and speciation. Hybridization may generate new genotypes with adaptive potential that did not reside as standing genetic variation in either parental population, potentially enhancing a population&apos;s responsiveness to selection. Our results make it conceivable that hybridization contributed to the rapid rates of phenotypic evolution in the large and rapid adaptive radiations of haplochromine cichlids.</description>
        <link>http://www.biomedcentral.com/1471-2148/9/283</link>
                <dc:creator>Rike Stelkens</dc:creator>
                <dc:creator>Corinne Schmid</dc:creator>
                <dc:creator>Oliver Selz</dc:creator>
                <dc:creator>Ole Seehausen</dc:creator>
                <dc:source>BMC Evolutionary Biology 2009, 9:283</dc:source>
        <dc:date>2009-12-04T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-2148-9-283</dc:identifier>
        <prism:publicationName>BMC Evolutionary Biology</prism:publicationName>
        <prism:issn>1471-2148</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>283</prism:startingPage>
        <prism:publicationDate>2009-12-04T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>PDF</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.biomedcentral.com/1471-2148/9/259">
        <title>Estimating the phylogeny and divergence times of primates using a supermatrix approach. </title>
        <description>Background:
The primates are among the most broadly studied mammalian orders, with the published literature containing extensive analyses of their behavior, physiology, genetics and ecology. The importance of this group in medical and biological research is well appreciated, and explains the numerous molecular phylogenies that have been proposed for most primate families and genera. Composite estimates for the entire order have been infrequently attempted, with the last phylogenetic reconstruction spanning the full range of primate evolutionary relationships having been conducted over a decade ago.
Results:
To estimate the structure and tempo of primate evolutionary history, we employed Bayesian phylogenetic methods to analyze data supermatrices comprising 7 mitochondrial genes (6,138 nucleotides) from 219 species across 67 genera and 3 nuclear genes (2,157 nucleotides) from 26 genera. Many taxa were only partially represented, with an average of 3.95 and 5.43 mitochondrial genes per species and per genus, respectively, and 2.23 nuclear genes per genus. Our analyses of mitochondrial DNA place Tarsiiformes as the sister group of Strepsirrhini. Within Haplorrhini, we find support for the primary divergence of Pitheciidae in Platyrrhini, and our results suggest a sister grouping of African and non-African colobines within Colobinae and of Cercopithecini and Papionini within Cercopthecinae. Date estimates for nodes within each family and genus are presented, with estimates for key splits including: Strepsirrhini-Haplorrhini 64 million years ago (MYA), Lemuriformes-Lorisiformes 52 MYA, Platyrrhini-Catarrhini 43 MYA and Cercopithecoidea-Hominoidea 29 MYA.
Conclusion:
We present an up-to-date, comprehensive estimate of the structure and tempo of primate evolutionary history. Although considerable gaps remain in our knowledge of the primate phylogeny, increased data sampling, particularly from nuclear loci, will be able to provide further resolution.</description>
        <link>http://www.biomedcentral.com/1471-2148/9/259</link>
                <dc:creator>Helen Chatterjee</dc:creator>
                <dc:creator>Simon Ho</dc:creator>
                <dc:creator>Ian Barnes</dc:creator>
                <dc:creator>Colin Groves</dc:creator>
                <dc:source>BMC Evolutionary Biology 2009, 9:259</dc:source>
        <dc:date>2009-10-27T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-2148-9-259</dc:identifier>
        <prism:publicationName>BMC Evolutionary Biology</prism:publicationName>
        <prism:issn>1471-2148</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>259</prism:startingPage>
        <prism:publicationDate>2009-10-27T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedcentral.com/1471-2148/9/280">
        <title>Toward reconstructing the evolution of advanced moths and butterflies (Lepidoptera: Ditrysia): an initial molecular study
</title>
        <description>Background:
In the mega-diverse insect order Lepidoptera (butterflies and moths; 165,000 described species), deeper relationships are little understood within the clade Ditrysia, to which 98% of the species belong. To begin addressing this problem, we tested the ability of five protein-coding nuclear genes (6.7 kb total), and character subsets therein, to resolve relationships among 123 species representing 27 (of 33) superfamilies and 55 (of 100) families of Ditrysia under maximum likelihood analysis.
Results:
Our trees show broad concordance with previous morphological hypotheses of ditrysian phylogeny, although most relationships among superfamilies are weakly supported. There are also notable surprises, such as a consistently closer relationship of Pyraloidea than of butterflies to most Macrolepidoptera. Monophyly is significantly rejected by one or more character sets for the putative clades Macrolepidoptera as currently defined (P &lt; 0.05) and Macrolepidoptera excluding Noctuoidea and Bombycoidea sensu lato (P [less than or equal to] 0.005), and nearly so for the superfamily Drepanoidea as currently defined (P &lt; 0.08). Superfamilies are typically recovered or nearly so, but usually without strong support. Relationships within superfamilies and families, however, are often robustly resolved. We provide some of the first strong molecular evidence on deeper splits within Pyraloidea, Tortricoidea, Geometroidea, Noctuoidea and others.Separate analyses of mostly synonymous versus non-synonymous character sets  revealed notable differences (though not strong conflict), including a marked influence of compositional heterogeneity on apparent signal in the third codon position (nt3). As available model partitioning methods cannot correct for this variation, we assessed overall phylogeny resolution through separate examination of trees from each character set. Exploration of &quot;tree space&quot; with GARLI, using grid computing, showed that hundreds of searches are typically needed to find the best-feasible phylogeny estimate for these data.
Conclusions:
Our results (a) corroborate the broad outlines of the current working phylogenetic hypothesis for Ditrysia, (b) demonstrate that some prominent features of that hypothesis, including the position of the butterflies, need revision, and (c) resolve the majority of family and subfamily relationships within superfamilies as thus far sampled. Much further gene and taxon sampling will be needed, however, to strongly resolve individual deeper nodes.</description>
        <link>http://www.biomedcentral.com/1471-2148/9/280</link>
                <dc:creator>Jerome Regier</dc:creator>
                <dc:creator>Andreas Zwick</dc:creator>
                <dc:creator>Michael Cummings</dc:creator>
                <dc:creator>Akito Kawahara</dc:creator>
                <dc:creator>Soowon Cho</dc:creator>
                <dc:creator>Susan Weller</dc:creator>
                <dc:creator>Amanda Roe</dc:creator>
                <dc:creator>Joaquin Baixeras</dc:creator>
                <dc:creator>John Brown</dc:creator>
                <dc:creator>Cynthia Parr</dc:creator>
                <dc:creator>Donald Davis</dc:creator>
                <dc:creator>Marc Epstein</dc:creator>
                <dc:creator>Winifred Hallwachs</dc:creator>
                <dc:creator>Axel Hausmann</dc:creator>
                <dc:creator>Daniel Janzen</dc:creator>
                <dc:creator>Ian Kitching</dc:creator>
                <dc:creator>M Solis</dc:creator>
                <dc:creator>Shen-Horn Yen</dc:creator>
                <dc:creator>Adam Bazinet</dc:creator>
                <dc:creator>Charles Mitter</dc:creator>
                <dc:source>BMC Evolutionary Biology 2009, 9:280</dc:source>
        <dc:date>2009-12-02T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-2148-9-280</dc:identifier>
        <prism:publicationName>BMC Evolutionary Biology</prism:publicationName>
        <prism:issn>1471-2148</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>280</prism:startingPage>
        <prism:publicationDate>2009-12-02T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>PDF</prism:versionidentifier>
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