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		<title>BMC Evolutionary Biology - Most viewed articles</title>
		<link>http://www.biomedcentral.com/bmcevolbiol/mostviewed/</link>
		<description>Most viewed articles in last 30 days from BMC Evolutionary Biology (ISSN 1471-2148) published by 
				
				BioMed Central
		</description>
        <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
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				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2148/8/173"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2148/8/250"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2148/8/251"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2148/8/267"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2148/7/219"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2148/8/210"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2148/8/230"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2148/8/238"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2148/7/214"/>			    
            
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		<item rdf:about="http://www.biomedcentral.com/1471-2148/8/173">
            
            <title>Dopamine receptor genetic polymorphisms and body composition in undernourished pastoralists: An exploration of nutrition indices among nomadic and recently settled Ariaal men of northern Kenya</title>
			<description>Background:
Minor alleles of the human dopamine receptor polymorphisms, DRD2/TaqI A and DRD4/48 bp, are related to decreased functioning and/or numbers of their respective receptors and have been shown to be correlated with body mass, height and food craving. In addition, the 7R minor allele of the DRD4 gene is at a higher frequency in nomadic compared to sedentary populations. Here we examine polymorphisms in the DRD2 and DRD4 genes with respect to body mass index (BMI) and height among men in two populations of Ariaal pastoralists, one recently settled (n = 87) and the other still nomadic (n = 65). The Ariaal live in northern Kenya, are chronically undernourished and are divided socially among age-sets.
Results:
Frequencies of the DRD4/7R and DRD2/A1 alleles were 19.4% and 28.2%, respectively and did not differ between the nomadic and settled populations. BMI was higher in those with one or two DRD4/7R alleles in the nomadic population, but lower among the settled. Post-hoc analysis suggests that the DRD4 differences in BMI were due primarily to differences in fat free body mass. Height was unrelated to either DRD2/TaqI A or DRD4/48 bp genotypes.
Conclusion:
Our results indicate that the DRD4/7R allele may be more advantageous among nomadic than settled Ariaal men. This result suggests that a selective advantage mediated through behaviour may be responsible for the higher frequency of the 7R alleles in nomadic relative to sedentary populations around the world. In contrast to previous work, we did not find an association between DRD2 genotypes and height. Our results support the idea that human phenotypic expression of genotypes should be rigorously evaluated in diverse environments and genetic backgrounds.</description>
			<link>http://www.biomedcentral.com/1471-2148/8/173</link>		
			<dc:creator>Dan TA Eisenberg, Benjamin Campbell, Peter B Gray and Michael D Sorenson</dc:creator>
			<dc:source>BMC Evolutionary Biology 2008, 8:173</dc:source>
			<dc:subject>Number of accesses: 861</dc:subject>
			<dc:date>2008-06-10</dc:date>
			<dc:identifier>doi:10.1186/1471-2148-8-173</dc:identifier>
			
			
							
					<prism:publicationName>BMC Evolutionary Biology</prism:publicationName>
					
			
							
					<prism:issn>1471-2148</prism:issn>
					
			
							
					<prism:volume>8</prism:volume>
					
			
							
					<prism:startingPage>173</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-06-10</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2148/8/250">
            
            <title>Ancestry and evolution of a secretory pathway serpin</title>
			<description>Background:
The serpin (serine protease inhibitor) superfamily constitutes a class of functionally highly diverse proteins usually encompassing several dozens of paralogs in mammals. Though phylogenetic classification of vertebrate serpins into six groups based on gene organisation is well established, the evolutionary roots beyond the fish/tetrapod split are unresolved. The aim of this study was to elucidate the phylogenetic relationships of serpins involved in surveying the secretory pathway routes against uncontrolled proteolytic activity.
Results:
Here, rare genomic characters are used to show that orthologs of neuroserpin, a prominent representative of vertebrate group 3 serpin genes, exist in early diverging deuterostomes and probably also in cnidarians, indicating that the origin of a mammalian serpin can be traced back far in the history of eumetazoans. A C-terminal address code assigning association with secretory pathway organelles is present in all neuroserpin orthologs, suggesting that supervision of cellular export/import routes by antiproteolytic serpins is an ancient trait, though subtle functional and compartmental specialisations have developed during their evolution. The results also suggest that massive changes in the exon-intron organisation of serpin genes have occurred along the lineage leading to vertebrate neuroserpin, in contrast with the immediately adjacent PDCD10 gene that is linked to its neighbour at least since divergence of echinoderms. The intron distribution pattern of closely adjacent and co-regulated genes thus may experience quite different fates during evolution of metazoans.
Conclusion:
This study demonstrates that the analysis of microsynteny and other rare characters can provide insight into the intricate family history of metazoan serpins. Serpins with the capacity to defend the main cellular export/import routes against uncontrolled endogenous and/or foreign proteolytic activity represent an ancient trait in eukaryotes that has been maintained continuously in metazoans though subtle changes affecting function and subcellular location have evolved. It is shown that the intron distribution pattern of neuroserpin gene orthologs has undergone substantial rearrangements during metazoan evolution.</description>
			<link>http://www.biomedcentral.com/1471-2148/8/250</link>		
			<dc:creator>Abhishek Kumar and Hermann Ragg</dc:creator>
			<dc:source>BMC Evolutionary Biology 2008, 8:250</dc:source>
			<dc:subject>Number of accesses: 711</dc:subject>
			<dc:date>2008-09-15</dc:date>
			<dc:identifier>doi:10.1186/1471-2148-8-250</dc:identifier>
			
			
							
					<prism:publicationName>BMC Evolutionary Biology</prism:publicationName>
					
			
							
					<prism:issn>1471-2148</prism:issn>
					
			
							
					<prism:volume>8</prism:volume>
					
			
							
					<prism:startingPage>250</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-09-15</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2148/8/251">
            
            <title>Careful with understudied phyla: The case of chaetognath</title>
			<description>Background:
A recent study by Barth&#233;l&#233;my et al. described a set of ribosomal protein (RP) genes extracted from a collection of expressed sequence tags (ESTs) of the chaetognath (arrow worm) Spadella cephaloptera. Three main conclusions were drawn in this paper. First, the authors stated that RP genes present paralogous copies, which have arisen through allopolyploidization. Second, they reported two alternate nucleotide stretches conserved within the 5' untranslated regions (UTR) of multiple ribosomal cDNAs and they suggested that these motifs are involved in the differential transcriptional regulation of paralogous RP genes. Third, they claimed that the phylogenetic position of chaetognaths could not be accurately inferred from a RP dataset because of the persistence of two problems: a long branch attraction (LBA) artefact and a compositional bias.
Results:
We reconsider here the results described in Barth&#233;l&#233;my et al. and question the evidence on which they are based. We find that their evidence for paralogous copies relies on faulty PCR experiments since they attempted to amplify DNA fragments absent from the genomic template. Our PCR experiments proved that the conserved motifs in 5'UTRs that they targeted in their amplifications are added post-transcriptionally by a trans-splicing mechanism. Then, we showed that the lack of phylogenetic resolution observed by these authors is due to limited taxon sampling and not to LBA or to compositional bias. A ribosomal protein dataset thus fully supports the position of chaetognaths as sister group of all other protostomes. This reinterpretation demonstrates that the statements of Barth&#233;l&#233;my et al. should be taken with caution because they rely on inaccurate evidence.
Conclusion:
The genomic study of an unconventional model organism is a meaningful approach to understand the evolution of animals. However, the previous study came to incorrect conclusions on the basis of experiments that omitted validation procedures.</description>
			<link>http://www.biomedcentral.com/1471-2148/8/251</link>		
			<dc:creator>Ferdinand Marl&#233;taz and Yannick Le Parco</dc:creator>
			<dc:source>BMC Evolutionary Biology 2008, 8:251</dc:source>
			<dc:subject>Number of accesses: 710</dc:subject>
			<dc:date>2008-09-17</dc:date>
			<dc:identifier>doi:10.1186/1471-2148-8-251</dc:identifier>
			
			
							
					<prism:publicationName>BMC Evolutionary Biology</prism:publicationName>
					
			
							
					<prism:issn>1471-2148</prism:issn>
					
			
							
					<prism:volume>8</prism:volume>
					
			
							
					<prism:startingPage>251</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-09-17</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2148/8/267">
            
            <title>Prebiotic replicase evolution in a surface-bound metabolic system: parasites as a source of adaptive evolution</title>
			<description>Background:
The remarkable potential of recent forms of life for reliably passing on genetic information through many generations now depends on the coordinated action of thousands of specialized biochemical "machines" (enzymes) that were obviously absent in prebiotic times. Thus the question how a complicated system like the living cell could have assembled on Earth seems puzzling. In seeking for a scientific explanation one has to search for step-by-step evolutionary changes from prebiotic chemistry to the emergence of the first proto-cell.
Results:
We try to sketch a plausible scenario in the first half of the story by exploring the ecological feasibility of a mineral surface-bound prebiotic replicator system that facilitates a primitive metabolism. Metabolism is a hypothetical network of simple chemical reactions producing monomers for the template-copying of RNA-like replicators, which in turn catalyse metabolic reactions. Using stochastic cellular automata (SCA) simulations we show that the surface-bound metabolic replicator system is viable despite internal competition among the genes and that it also maintains a set of mild "parasitic" sequences which occasionally evolve functions such as that of a replicase.
Conclusion:
Replicase activity is shown to increase even at the expense of slowing down the replication of the evolving ribozyme itself, due to indirect mutualistic benefits in a diffuse form of group selection among neighbouring replicators. Finally we suggest possible paths for further evolutionary changes in the metabolic replicator system leading to increased metabolic efficiency, improved replicase functionality, and membrane production.</description>
			<link>http://www.biomedcentral.com/1471-2148/8/267</link>		
			<dc:creator>Balazs Konnyu, Tamas Czaran and Eors Szathmary</dc:creator>
			<dc:source>BMC Evolutionary Biology 2008, 8:267</dc:source>
			<dc:subject>Number of accesses: 677</dc:subject>
			<dc:date>2008-09-30</dc:date>
			<dc:identifier>doi:10.1186/1471-2148-8-267</dc:identifier>
			
			
							
					<prism:publicationName>BMC Evolutionary Biology</prism:publicationName>
					
			
							
					<prism:issn>1471-2148</prism:issn>
					
			
							
					<prism:volume>8</prism:volume>
					
			
							
					<prism:startingPage>267</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-09-30</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<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 and Jean-Marie Beckerich</dc:creator>
			<dc:source>BMC Evolutionary Biology 2007, 7:219</dc:source>
			<dc:subject>Number of accesses: 649</dc:subject>
			<dc:date>2007-11-12</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>2007-11-12</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2148/8/210">
            
            <title>The molecular basis of color vision in colorful fish: Four Long Wave-Sensitive (LWS) opsins in guppies (Poecilia reticulata) are defined by amino acid substitutions at key functional sites</title>
			<description>Background:
Comparisons of functionally important changes at the molecular level in model systems have identified key adaptations driving isolation and speciation. In cichlids, for example, long wavelength-sensitive (LWS) opsins appear to play a role in mate choice and male color variation within and among species. To test the hypothesis that the evolution of elaborate coloration in male guppies (Poecilia reticulata) is also associated with opsin gene diversity, we sequenced long wavelength-sensitive (LWS) opsin genes in six species of the family Poeciliidae.
Results:
Sequences of four LWS opsin genes were amplified from the guppy genome and from mRNA isolated from adult guppy eyes. Variation in expression was quantified using qPCR. Three of the four genes encode opsins predicted to be most sensitive to different wavelengths of light because they vary at key amino acid positions. This family of LWS opsin genes was produced by a diversity of duplication events. One, an intronless gene, was produced prior to the divergence of families Fundulidae and Poeciliidae. Between-gene PCR and DNA sequencing show that two of the guppy LWS opsins are linked in an inverted orientation. This inverted tandem duplication event occurred near the base of the poeciliid tree in the common ancestor of Poecilia and Xiphophorus. The fourth sequence has been uncovered only in the genus Poecilia. In the guppies surveyed here, this sequence is a hybrid, with the 5' end most similar to one of the tandem duplicates and the 3' end identical to the other.
Conclusion:
Enhanced wavelength discrimination, a possible consequence of opsin gene duplication and divergence, might have been an evolutionary prerequisite for color-based sexual selection and have led to the extraordinary coloration now observed in male guppies and in many other poeciliids.</description>
			<link>http://www.biomedcentral.com/1471-2148/8/210</link>		
			<dc:creator>Matthew N Ward, Allison M Churcher, Kevin J Dick, Chris RJ Laver, Greg L Owens, Megan D Polack, Pam R Ward, Felix Breden and John S Taylor</dc:creator>
			<dc:source>BMC Evolutionary Biology 2008, 8:210</dc:source>
			<dc:subject>Number of accesses: 616</dc:subject>
			<dc:date>2008-07-18</dc:date>
			<dc:identifier>doi:10.1186/1471-2148-8-210</dc:identifier>
			
			
							
					<prism:publicationName>BMC Evolutionary Biology</prism:publicationName>
					
			
							
					<prism:issn>1471-2148</prism:issn>
					
			
							
					<prism:volume>8</prism:volume>
					
			
							
					<prism:startingPage>210</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-07-18</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2148/8/230">
            
            <title>The earliest settlers' antiquity and evolutionary history of Indian populations: evidence from M2 mtDNA lineage</title>
			<description>Background:
The "out of Africa" model postulating single "southern route" dispersal posits arrival of "Anatomically Modern Human" to Indian subcontinent around 66&#8211;70 thousand years before present (kyBP). However the contributions and legacy of these earliest settlers in contemporary Indian populations, owing to the complex past population dynamics and later migrations has been an issue of controversy. The high frequency of mitochondrial lineage "M2" consistent with its greater age and distribution suggests that it may represent the phylogenetic signature of earliest settlers. Accordingly, we attempted to re-evaluate the impact and contribution of earliest settlers in shaping the genetic diversity and structure of contemporary Indian populations; using our newly sequenced 72 and 4 published complete mitochondrial genomes of this lineage.
Results:
The M2 lineage, harbouring two deep rooting subclades M2a and M2b encompasses approximately one tenth of the mtDNA pool of studied tribes. The phylogeographic spread and diversity indices of M2 and its subclades among the tribes of different geographic regions and linguistic phyla were investigated in detail. Further the reconstructed demographic history of M2 lineage as a surrogate of earliest settlers' component revealed that the demographic events with pronounced regional variations had played pivotal role in shaping the complex net of populations phylogenetic relationship in Indian subcontinent.
Conclusion:
Our results suggest that tribes of southern and eastern region along with Dravidian and Austro-Asiatic speakers of central India are the modern representatives of earliest settlers of subcontinent. The Last Glacial Maximum aridity and post LGM population growth mechanised some sort of homogeneity and redistribution of earliest settlers' component in India. The demic diffusion of agriculture and associated technologies around 3 kyBP, which might have marginalized hunter-gatherer, is coincidental with the decline of earliest settlers' population during this period.</description>
			<link>http://www.biomedcentral.com/1471-2148/8/230</link>		
			<dc:creator>Satish Kumar, PBSV Padmanabham, Rajasekhara R Ravuri, Kiran Uttaravalli, Padmaja Koneru, P Aditi Mukherjee, B Das, M Kotal, D Xaviour, SY Saheb and VR Rao</dc:creator>
			<dc:source>BMC Evolutionary Biology 2008, 8:230</dc:source>
			<dc:subject>Number of accesses: 608</dc:subject>
			<dc:date>2008-08-11</dc:date>
			<dc:identifier>doi:10.1186/1471-2148-8-230</dc:identifier>
			
			
							
					<prism:publicationName>BMC Evolutionary Biology</prism:publicationName>
					
			
							
					<prism:issn>1471-2148</prism:issn>
					
			
							
					<prism:volume>8</prism:volume>
					
			
							
					<prism:startingPage>230</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-08-11</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2148/8/238">
            
            <title>The coevolution of cooperation and dispersal in social groups and its implications for the emergence of multicellularity</title>
			<description>Background:
Recent work on the complexity of life highlights the roles played by evolutionary forces at different levels of individuality. One of the central puzzles in explaining transitions in individuality for entities ranging from complex cells, to multicellular organisms and societies, is how different autonomous units relinquish control over their functions to others in the group. In addition to the necessity of reducing conflict over effecting specialized tasks, differentiating groups must control the exploitation of the commons, or else be out-competed by more fit groups.
Results:
We propose that two forms of conflict &#8211; access to resources within groups and representation in germ line &#8211; may be resolved in tandem through individual and group-level selective effects. Specifically, we employ an optimization model to show the conditions under which different within-group social behaviors (cooperators producing a public good or cheaters exploiting the public good) may be selected to disperse, thereby not affecting the commons and functioning as germ line. We find that partial or complete dispersal specialization of cheaters is a general outcome. The propensity for cheaters to disperse is highest with intermediate benefit:cost ratios of cooperative acts and with high relatedness. An examination of a range of real biological systems tends to support our theory, although additional study is required to provide robust tests.
Conclusion:
We suggest that trait linkage between dispersal and cheating should be operative regardless of whether groups ever achieve higher levels of individuality, because individual selection will always tend to increase exploitation, and stronger group structure will tend to increase overall cooperation through kin selected benefits. Cheater specialization as dispersers offers simultaneous solutions to the evolution of cooperation in social groups and the origin of specialization of germ and soma in multicellular organisms.</description>
			<link>http://www.biomedcentral.com/1471-2148/8/238</link>		
			<dc:creator>Michael E Hochberg, Daniel J Rankin and Michael Taborsky</dc:creator>
			<dc:source>BMC Evolutionary Biology 2008, 8:238</dc:source>
			<dc:subject>Number of accesses: 593</dc:subject>
			<dc:date>2008-08-19</dc:date>
			<dc:identifier>doi:10.1186/1471-2148-8-238</dc:identifier>
			
			
							
					<prism:publicationName>BMC Evolutionary Biology</prism:publicationName>
					
			
							
					<prism:issn>1471-2148</prism:issn>
					
			
							
					<prism:volume>8</prism:volume>
					
			
							
					<prism:startingPage>238</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-08-19</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<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 J Drummond and Andrew Rambaut</dc:creator>
			<dc:source>BMC Evolutionary Biology 2007, 7:214</dc:source>
			<dc:subject>Number of accesses: 584</dc:subject>
			<dc:date>2007-11-08</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>2007-11-08</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2148/8/248">
            
            <title>Meta-population structure in a coral reef fish demonstrated by genetic data on patterns of migration, extinction and re-colonisation</title>
			<description>Background:
Management strategies for coral reefs are dependant on information about the spatial population structure and connectivity of reef organisms. Genetic tools can reveal important information about population structure, however, this information is lacking for many reef species. We used a mitochondrial molecular marker to examine the population genetic structure and the potential for meta-population dynamics in a direct developing coral reef fish using 283 individuals from 15 reefs on the Great Barrier Reef, Australia. We employed a hierarchical sampling design to test genetic models of population structure at multiple geographical scales including among regions, among shelf position and reefs within regions. Predictions from island, isolation-by-distance and meta-population models, including the potential for asymmetric migration, local extinction and patterns of re-colonisation were examined.
Results:
Acanthochromis polyacanthus displayed strong genetic structure among regions (&#934;ST = 0.81, P &lt; 0.0001) that supported an equilibrium isolation-by-distance model (r = 0.77, P = 0.001). Significant structuring across the continental shelf was only evident in the northern region (&#934;ST = 0.31, P &lt; 0.001) and no evidence of isolation-by-distance was found within any region. Pairwise &#934;ST values indicated overall strong but variable genetic structure (mean &#934;ST among reefs within regions = 0.28, 0.38, 0.41), and asymmetric migration rates among reefs with low genetic structure. Genetic differentiation among younger reefs was greater than among older reefs supporting a meta-population propagule-pool colonisation model. Variation in genetic diversities, demographic expansion and population growth estimates indicated more frequent genetic bottlenecks/founder effects and subsequent population expansion in the central and southern regions compared to the northern one.
Conclusion:
Our findings provide genetic evidence for meta-population dynamics in a direct developing coral reef fish and we reject the equilibrium island and isolation-by distance models at local spatial scales. Instead, strong non-equilibrium genetic structure appears to be generated by genetic bottlenecks/founder effects associated with population reductions/extinctions and asymmetric migration/(re)-colonisation of such populations. These meta-population dynamics varied across the geographical range examined with edge populations exhibiting lower genetic diversities and higher rates of population expansion than more central populations. Therefore, coral reef species may experience local population reductions/extinctions that promote overall meta-population genetic differentiation.</description>
			<link>http://www.biomedcentral.com/1471-2148/8/248</link>		
			<dc:creator>Line K Bay, M Julian Caley and Ross H Crozier</dc:creator>
			<dc:source>BMC Evolutionary Biology 2008, 8:248</dc:source>
			<dc:subject>Number of accesses: 579</dc:subject>
			<dc:date>2008-09-12</dc:date>
			<dc:identifier>doi:10.1186/1471-2148-8-248</dc:identifier>
			
			
							
					<prism:publicationName>BMC Evolutionary Biology</prism:publicationName>
					
			
							
					<prism:issn>1471-2148</prism:issn>
					
			
							
					<prism:volume>8</prism:volume>
					
			
							
					<prism:startingPage>248</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-09-12</prism:publicationDate>
					

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