Show simple item record

Hidden Floridian biodiversity: mitochondrial and nuclear gene trees reveal four cryptic species within the scorched mussel, Brachidontes exustus , species complex

dc.contributor.authorLee, Taehwanen_US
dc.contributor.authorÓ Foighil, Diarmaiden_US
dc.date.accessioned2010-06-01T19:24:14Z
dc.date.available2010-06-01T19:24:14Z
dc.date.issued2004-11en_US
dc.identifier.citationLEE, T.; Ó FOIGHIL, D. (2004). "Hidden Floridian biodiversity: mitochondrial and nuclear gene trees reveal four cryptic species within the scorched mussel, Brachidontes exustus , species complex." Molecular Ecology 13(11): 3527-3542. <http://hdl.handle.net/2027.42/72545>en_US
dc.identifier.issn0962-1083en_US
dc.identifier.issn1365-294Xen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/72545
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=15488009&dopt=citationen_US
dc.description.abstractThe well-documented Floridian ‘Gulf/Atlantic’ marine genetic disjunction provides an influential example of vicariant cladogenesis along a continental coastline for major elements of a diverse nearshore fauna. We are engaged in a two-part study that aims to place this disjunction into a regional Caribbean Basin phylogenetic perspective using the scorched mussel Brachidontes exustus as an exemplar. Our first step, documented here, is to thoroughly characterize the genetic structure of Floridian scorched mussel populations using mitochondrial (mt) and nuclear markers. Both sets of markers recovered the expected disjunction involving sister clades distributed on alternate flanks of peninsular Florida and lineage-specific mt molecular clocks placed its origin in the Pliocene. The two sister clades had distinct population genetic profiles and the Atlantic clade appears to have experienced an evolutionarily recent bottleneck, although plots of the relative estimates of N through time are consistent with its local persistence through the last Ice Age Maximum. Our primary novel result, however, was the discovery that the Gulf/Atlantic disjunction represents but one of three cryptic, nested genetic discontinuities represented in Floridian scorched mussel populations. The most pronounced phylogenetic split distinguished the Gulf and Atlantic sister clades from two additional nested cryptic sister clades present in samples taken from the southern Florida tropical marine zone. Floridian populations of B. exustus are composed of four cryptic taxa, a result consistent with the hypothesis that the Gulf/Atlantic disjunction in this morphospecies is but one of multiple latent regional genetic breakpoints.en_US
dc.format.extent406979 bytes
dc.format.extent3109 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Science Ltden_US
dc.rights© 2004 Blackwell Publishing Ltden_US
dc.subject.otherBivalviaen_US
dc.subject.otherCaribbeanen_US
dc.subject.otherCarolinianen_US
dc.subject.otherGenetic Disjunctionen_US
dc.subject.otherPhylogenyen_US
dc.subject.otherSibling Speciesen_US
dc.titleHidden Floridian biodiversity: mitochondrial and nuclear gene trees reveal four cryptic species within the scorched mussel, Brachidontes exustus , species complexen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelEcology and Evolutionary Biologyen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumMuseum of Zoology and Department of Ecology and Evolutionary Biology, University of Michigan, 1109 Geddes Avenue, Ann Arbor, MI 48109-1079, USAen_US
dc.identifier.pmid15488009en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/72545/1/j.1365-294X.2004.02337.x.pdf
dc.identifier.doi10.1111/j.1365-294X.2004.02337.xen_US
dc.identifier.sourceMolecular Ecologyen_US
dc.identifier.citedreferenceAbbott RT ( 1974 ) American Seashells. Van Nostrand Reinhold, New York, NY.en_US
dc.identifier.citedreferenceAtkinson LP, Lee TN, Blanton JO, Chandler WS ( 1983 ) Climatology of the southeastern United States continental shelf waters. Journal of Geophysical Research, 88, 4705 – 4718.en_US
dc.identifier.citedreferenceAvise JC ( 1992 ) Molecular population structure and the biogeographic history of a regional fauna: a case history with lessons for conservation biology. Oikos, 63, 62 – 76.en_US
dc.identifier.citedreferenceAvise JC ( 1994 ) Molecular Markers, Natural History and Evolution. Chapman & Hall, New York, NY.en_US
dc.identifier.citedreferenceAvise JC ( 2000 ) Phylogeography. The History and Formation of Species. Harvard University Press, Cambridge, MA.en_US
dc.identifier.citedreferenceAvise JC, Reeb CA, Saunders NC ( 1987 ) Geographic population structure and species differences in mitochondrial DNA of mouthbrooding marine catfishes (Ariidae) and demersal spawning toadfishes (Batrachoididae). Evolution, 41, 991 – 1002.en_US
dc.identifier.citedreferenceBeckenbach AT ( 1994 ) Mitochondrial haplotype frequencies in oysters: neutral alternatives to selection models. In: Non-Neutral Evolution: Theories and Molecular Data (ed. Golding B ), pp. 188 – 198. Chapman & Hall, New York, NY.en_US
dc.identifier.citedreferenceBenzie JAH ( 1999 ) Genetic structure of coral reef organisms: ghosts of dispersal past. American Zoologist, 39, 131 – 145.en_US
dc.identifier.citedreferenceBert TM ( 1986 ) Speciation in western Atlantic stone crabs (genus Menippe ): the role of geological processes and climatic events in the formation and distribution of species. Marine Biology, 93, 157 – 170.en_US
dc.identifier.citedreferenceBert TM, Arnold WS ( 1995 ) An empirical test of predictions of two competing models for the maintenance and fate of hybrid zones: both models are supported in a hard clam hybrid zone. Evolution, 49, 276 – 289.en_US
dc.identifier.citedreferenceBert TM, Harrison RG ( 1988 ) Hybridization in western Atlantic stone crabs (genus Menippe ): evolutionary history and ecological context influence species interactions. Evolution, 42, 528 – 544.en_US
dc.identifier.citedreferenceBorsa P, Naciri M, Bahiri L et al. ( 1997 ) Infraspecific zoogeography of the Mediterranean: population genetic analysis on sixteen Atlanto-Mediterranean species (fishes and invertebrates). Vie Milieu, 47, 295 – 305.en_US
dc.identifier.citedreferenceBriggs JC ( 1970 ) A faunal history of the North Atlantic Ocean. Systematic Zoology, 19, 19 – 34.en_US
dc.identifier.citedreferenceBriggs JC ( 1974 ) Marine Zoogeography. McGraw-Hill, New York, NY.en_US
dc.identifier.citedreferenceChase MR, Etter RJ, Rex MA, Quattro JM ( 1998 ) Bathymetric patterns of genetic variation in a deep-sea protobranch bivalve, Demninucula atacellana. Marine Biology, 131, 301 – 308.en_US
dc.identifier.citedreferenceClement M, Posada D, Crandall KA ( 2000 ) tcs: a computer program to estimate gene genealogies. Molecular Ecology, 9, 1657 – 1660.en_US
dc.identifier.citedreferenceCoan EV, Scott PV, Bernard FR ( 2000 ) Bivalve Seashells of North America. Santa Barbara Museum of Natural History, Santa Barbara, CA.en_US
dc.identifier.citedreferenceCoates AG, Jackson JBC, Collins LS et al. ( 1992 ) Closure of the Isthmus of Panama: the near-shore marine record of Costa Rica and western Panama. Geological Society of America Bulletin, 104, 814 – 828.en_US
dc.identifier.citedreferenceCollin R ( 2001 ) The effects of mode of development on phylogeography and population structure of North Atlantic Crepidula (Gastropoda: Calyptraeidae). Molecular Ecology, 10, 2249 – 2262.en_US
dc.identifier.citedreferenceCollin R ( 2002 ) Another last word on Crepidula convexa with a description of C. ustulatulina n. sp. (Gastropoda: Calyptraeidae) from the Gulf of Mexico and southern Florida. Bulletin of Marine Science, 70, 177 – 184.en_US
dc.identifier.citedreferenceCracraft J ( 1994 ) Species diversity, biogeography and the evolution of biotas. American Zoologist, 34, 33 – 47.en_US
dc.identifier.citedreferenceCroizat L, Nelson G, Rosen DE ( 1974 ) Centers of origin and related concepts. Systematic Zoology, 23, 265 – 287.en_US
dc.identifier.citedreferenceCronin TM ( 1988 ) Evolution of marine climates of the US Atlantic coast during the past four million years. Philosophical Transactions of the Royal Society of London B, 318, 661 – 678.en_US
dc.identifier.citedreferenceCunningham CW, Collins TM ( 1994 ) Developing model systems for molecular biogeography: vicariance and interchange in marine invertebrates. In: Molecular Ecology and Evolution: Approaches and Applications (eds Schierwater B, Streit B, Wagner GP, DeSalle R ), pp. 405 – 433. Birkhauser Verlag Basel, Basel.en_US
dc.identifier.citedreferenceCunningham CW, Buss LW, Anderson CW ( 1991 ) Molecular and geological evidence of shared history between hermit crabs and the symbiotic genus Hydractinia. Evolution, 458, 1301 – 1316.en_US
dc.identifier.citedreferenceDistel DL ( 2000 ) Phylogenetic relationships among Mytilidae (Bivalvia): 18S rRNA data suggest convergence in mytilid body plans. Molecular Phylogenetics and Evolution, 15, 25 – 33.en_US
dc.identifier.citedreferenceDroxler AW, Burke K, Cunningham AD et al. ( 1998 ) Caribbean constraints on circulation between Atlantic and Pacific oceans over the past 40 million years. In: Tectonic Boundary Conditions for Climate Reconstruction (eds Crowley T, Burke K ), pp. 160 – 191. Oxford University Press, Oxford.en_US
dc.identifier.citedreferenceDuggins CF, Karlin AA, Mousseau TA, Relyea KG ( 1995 ) Analysis of a hybrid zone in Fundulus majalis in a northeastern Florida ecotone. Heredity, 74, 117 – 128.en_US
dc.identifier.citedreferenceEdwards S, Beerli P ( 2000 ) Gene divergence, population divergence, and the variance in coalescence time in phylogeographic studies. Evolution, 54, 1839 – 1854.en_US
dc.identifier.citedreferenceExcoffier L, Smouse PE, Quattro JM ( 1992 ) Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data. Genetics, 131, 45479 – 45491.en_US
dc.identifier.citedreferenceFarris JS, KÄllersjÖ M, Kluge AG, Bult C ( 1995 ) Testing significance of congruence. Cladistics, 10, 315 – 319.en_US
dc.identifier.citedreferenceFelder DL, Staton JL ( 1994 ) Genetic differentiation in the Gulf–Atlantic species complexes of Sesarma and Uca (Crustacea: Decapoda: Brachyura). Journal of Crustacean Biology, 14, 191 – 209.en_US
dc.identifier.citedreferenceFelsenstein J ( 1981 ) Evolutionary trees from DNA sequences: a maximum likelihood approach. Journal of Molecular Evolution, 32, 79 – 81.en_US
dc.identifier.citedreferenceFelsenstein J ( 1985 ) Confidence limits on phylogenies: an approach using the bootstrap. Evolution, 39, 783 – 791.en_US
dc.identifier.citedreferenceFisher C, Skibinski DOF ( 1990 ) Sex-biased mitochondrial DNA heteroplasmy in the marine mussel Mytilus. Proceedings of the Royal Society London Series B, 242, 149 – 156.en_US
dc.identifier.citedreferenceÓ Foighil D, Hilbish TJ, Showman RM ( 1996 ) Mitochondrial gene variation in Mercenaria clam sibling species reveals a relict secondary contact zone in the western Gulf of Mexico. Marine Biology, 126, 675 – 683.en_US
dc.identifier.citedreferenceÓ Foighil D, Marshall BA, Hilbish TJ, Pino MA ( 1999 ) Trans-Pacific range extension by rafting is inferred for the flat oyster Ostrea chilensis. Biology Bulletin, 196, 122 – 126.en_US
dc.identifier.citedreferenceFolmer O, Black M, Hoeh W, Lutz R, Vrijenhork R ( 1994 ) DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Molecular Marine Biology and Biotechnology, 3, 294 – 299.en_US
dc.identifier.citedreferenceGeller JB ( 1994 ) Sex-specific mitochondrial DNA haplotypes and heteroplasmy in Mytilus trossulus and Mytilus galloprovincialis populations. Molecular Marine Biology and Biotechnology, 3, 334 – 337.en_US
dc.identifier.citedreferenceGold JR, Richardson LR ( 1998 ) Mitochondrial DNA diversification and population structure in fishes from the Gulf of Mexico and western Atlantic. Journal of Heredity, 89, 404 – 414.en_US
dc.identifier.citedreferenceGopurenko D, Hughes JM, Keenan CP ( 1999 ) Mitochondrial DNA evidence for rapid colonization of the Indo-West Pacific by the mudcrab Scylla serrata. Marine Biology, 134, 227 – 233.en_US
dc.identifier.citedreferenceGrosberg R, Cunningham CW ( 2001 ) Genetic structure in the sea from populations to communities. In: Marine Community Ecology (eds Bertness MD, Gaines SD, Hay ME ), pp. 61 – 84. Sinauer Associates Inc., Sunderland, MA.en_US
dc.identifier.citedreferenceGurgel CFD, Fredericq S, Norris JN ( 2004 ) Phylogeography of Gracilaria tikvahiae (Gracilariaceae, Rhodophyta): a study of a genetic discontinuity in a continuously distributed species based on molecular evidence. Journal of Phycology, 40, 748 – 758.en_US
dc.identifier.citedreferenceHare MP, Avise JC ( 1996 ) Molecular genetic analysis of a stepped multilocus cline in the American oyster ( Crassostrea virginica ). Evolution, 50, 2305 – 2315.en_US
dc.identifier.citedreferenceHare MP, Avise JC ( 1998 ) Population structure in the American oyster as inferred by nuclear gene genealogies. Molecular Biology and Evolution, 15, 119 – 128.en_US
dc.identifier.citedreferenceHare MP, Karl SA, Avise JC ( 1996 ) Anonymous nuclear DNA markers in the American oyster and their implications for the heterozygote deficiency phenomenon in marine bivalves. Molecular Biology and Evolution, 13, 334 – 345.en_US
dc.identifier.citedreferenceHillis DM, Mable BK, Moritz C ( 1996 ) Applications of molecular systematics. In: Molecular Systematics (eds Hillis DM, Moritz C, Mable BK ), pp. 515 – 530. Sinauer Associates, Sunderland, MA.en_US
dc.identifier.citedreferenceHoeh WR, Blakley KH, Brown WM ( 1991 ) Heteroplasmy suggests limited biparental inheritance of Mytilus mitochondrial DNA. Science, 251, 1488 – 1490.en_US
dc.identifier.citedreferenceHoeh WR, Stewart DT, Sutherland BW, Saavedra C, Zouros E ( 1997 ) Phylogenetic evidence for role-reversals of gender-associated mitochondrial DNA in Mytilus. Molecular Biology and Evolution, 14, 959 – 967.en_US
dc.identifier.citedreferenceIturralde-Vinent MA, MacPhee RDE ( 1999 ) Paleogeography of the Caribbean region: implications for Cenozoic biogeography. Bulletin of the American Museum of Natural History, 283, 1 – 95.en_US
dc.identifier.citedreferenceKarl SA, Avise JC ( 1992 ) Balancing selection at allozyme loci in oysters: implications from nuclear RFLPs. Science, 256, 100 – 102.en_US
dc.identifier.citedreferenceKirkendale L, Lee T, Baker PÓ, Foighil D ( 2004 ) Oysters of the Conch Republic (Florida Keys); a molecular phylogenetic study of Parahyotissa mcgintyi, Teskeyostrea weberi and Ostreola equestris. Malacologia, 46, in press.en_US
dc.identifier.citedreferenceKnowlton N ( 1993 ) Sibling species in the sea. Annual Review of Ecology and Systematics, 24, 189 – 216.en_US
dc.identifier.citedreferenceKnowlton N ( 2000 ) Molecular genetic analyses of species boundaries in the sea. Hydrobiologia, 420, 73 – 90.en_US
dc.identifier.citedreferenceKohn AJ, Perron FE ( 1994 ) Life History and Biogeography Patterns in Conus. Oxford Biogeography Series 9. Clarendon Press, Oxford.en_US
dc.identifier.citedreferenceKuhner MK, Yamato J, Felsenstein J ( 1998 ) Maximum likelihood estimation of population growth rates based on the coalescent. Genetics, 149, 429 – 434.en_US
dc.identifier.citedreferenceLavery S, Moritz C, Fielder DR ( 1996 ) Genetic patterns suggest exponential population growth in a declining species. Molecular Biology and Evolution, 13, 1106 – 1113.en_US
dc.identifier.citedreferenceLee T, Ó Foighil D ( 2003 ) Phylogenetic structure of the Sphaeriinae, a global clade of freshwater bivalve molluscs, inferred from nuclear (ITS-1) and mitochondrial (16S) ribosomal gene sequences. Zoological Journal of the Linnean Society, 137, 245 – 260.en_US
dc.identifier.citedreferenceLessios HA, Kessing BD, Robertson DR ( 1998 ) Massive gene flow across the world's most potent marine biogeographic barrier. Proceedings of the Royal Society London Series B, 265, 583 – 588.en_US
dc.identifier.citedreferenceLessios HA, Kessing BD, Robertson DR, Paulay G ( 1999 ) Phylogeography of the pantropical sea urchin Eucidaris in relation to land barriers and ocean currents. Evolution, 53, 806 – 817.en_US
dc.identifier.citedreferenceLiu HP, Mitton JB, Wu SK ( 1996 ) Paternal mitochondrial DNA differentiation far exceeds maternal mitochondrial DNA and allozyme differentiation in the freshwater mussel, Anodonta grandis grandis. Evolution, 50, 952 – 957.en_US
dc.identifier.citedreferenceMarko PB ( 2002 ) Fossil calibration of molecular clocks and the divergence times of geminate species pairs separated by the Isthmus of Panama. Molecular Biology and Evolution, 19, 2005 – 2021.en_US
dc.identifier.citedreferenceMarshall LG ( 1988 ) Land mammals and the Great American Interchange. American Scientist, 76, 380 – 388.en_US
dc.identifier.citedreferenceMcDonald JH, Verrelli BC, Geyer LB ( 1996 ) Lack of geographic variation in anonymous nuclear polymorphisms in the American oyster, Crassostrea virginica. Molecular Biology and Evolution, 13, 1114 – 1118.en_US
dc.identifier.citedreferenceMikkelsen PM, Bieler R ( 2000 ) Marine bivalves of the Florida Keys: discovered biodiversity. In: The Evolutionary Biology of the Bivalvia (eds Harper EM, Taylor JD, Crame JA ), Geological Society of London. Special Publications, 177, 367 – 387.en_US
dc.identifier.citedreferenceMorton B ( 1988 ) The population dynamics and reproductive cycle of Brachidontes variabilis (Bivalvia: Mytilidae) in a Hong Kong mangrove. Malacological Review, 21, 109 – 117.en_US
dc.identifier.citedreferenceNei M ( 1987 ) Molecular Evolutionary Genetics. Columbia University Press, New York, NY.en_US
dc.identifier.citedreferenceNei M, Li W-H ( 1979 ) Mathematical model for studying genetic variation in terms of restriction endonuclease. Proceedings of the National Academy of Sciences of the USA, 76, 5269 – 5273.en_US
dc.identifier.citedreferenceNeigel JE, Avise JC ( 1986 ) Phylogenetic relationships of mitochondrial DNA under various demographic models of speciation. In: Evolutionary Processes and Theory (eds Nevo E, Karlin S ), pp. 515 – 534. Academic Press, New York, NY.en_US
dc.identifier.citedreferencePalumbi SR ( 1992 ) Speciation on a small planet. Trends in Ecology and Evolution, 7, 114 – 118.en_US
dc.identifier.citedreferencePalumbi SR ( 1994 ) Genetic divergence, reproductive isolation, and marine speciation. Annual Review of Ecology and Systematics, 25, 547 – 572.en_US
dc.identifier.citedreferencePark J-K, Ó Foighil D ( 2000 ) Sphaeriid and corbiculid clams represent separate heterodont bivalve radiations into freshwater environments. Molecular Phylogenetics and Evolution, 14, 75 – 88.en_US
dc.identifier.citedreferencePassamonti M, Boore JL, Scali V ( 2003 ) Molecular evolution and recombination in gender-associated mitochondrial DNAs of the Manila clam Tapes philippinarum. Genetics, 164, 603 – 611.en_US
dc.identifier.citedreferencePielou EC ( 1991 ) After the Ice Age. University of Chicago Press, Chicago, IL.en_US
dc.identifier.citedreferencePosada D, Crandall KA ( 1998 ) modeltest: testing the model of DNA substitution. Bioinformatics, 14, 817 – 818.en_US
dc.identifier.citedreferencePosada D, Crandall KA ( 2001 ) Selecting models of nucleotide substitution: An application to human immunodeficiency virus 1 (HIV-1). Molecular Biology and Evolution, 18, 897 – 906.en_US
dc.identifier.citedreferenceQuesada H, Skibinski DAG, Skibinski DOF ( 1996 ) Sex-biased heteroplasmy and mitochondrial DNA inheritance in the mussel Mytilus galloprovincialis Lmk. Current Genetics, 29, 423 – 426.en_US
dc.identifier.citedreferenceQuesada H, Stuckas H, Skibinski DOF ( 2003 ) Heteroplasmy suggests paternal co-transmission of multiple genomes and pervasive reversion of maternally into paternally transmitted genomes of mussel ( Mytilus ) mitochondrial DNA. Journal of Molecular Evolution, 57, S138 – S147.en_US
dc.identifier.citedreferenceRandazzo AF, Jones DS ( 1997 ) The Geology of Florida. University Press of Florida, Gainesville, FL.en_US
dc.identifier.citedreferenceRawson PD, Hilbish. TJ ( 1995 ) Evolutionary relationships among the male and female mitochondrial DNA lineages in the Mytilus edulis species complex. Molecular Biology and Evolution, 12, 893 – 901.en_US
dc.identifier.citedreferenceReeb CA, Avise JC ( 1990 ) A genetic discontinuity in a continuously distributed species: mitochondrial DNA in the American oyster, Crassostrea virginica. Genetics, 124, 397 – 406.en_US
dc.identifier.citedreferenceRonquist F, Huelsenbeck JP ( 2003 ) mrbayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics, 19, 1572 – 1574.en_US
dc.identifier.citedreferenceSarver SK, Landrum MC, Foltz DW ( 1992 ) Genetics and taxonomy of ribbed mussels ( Geukensia spp.). Marine Biology, 113, 385 – 390.en_US
dc.identifier.citedreferenceSaunders NC, Kessler LG, Avise JC ( 1986 ) Genetic variation and geographic differentiation in mitochondrial DNA of the horseshoe crab, Limulus polyphemus. Genetics, 112, 613 – 627.en_US
dc.identifier.citedreferenceSchizas NV, Street GT, Coul BC, Chandler GT, Quattro JM ( 1999 ) Molecular population structure of the marine benthic copepod Microarthridion littorale along the southeastern and Gulf coasts of the USA. Marine Biology, 135, 399 – 405.en_US
dc.identifier.citedreferenceSchneider S, Roessli D, Excoffier L ( 2000 ) arlequin: a Software for Population Genetics Data Analysis, Version 2.000. Genetics and Biometry Laboratory, University of Geneva, Switzerland.en_US
dc.identifier.citedreferenceSkibinski DOF, Gallagher C, Benyon CM ( 1994 ) Mitochondrial DNA inheritance. Nature, 368, 817 – 818.en_US
dc.identifier.citedreferenceSkibinski DOF, Gallagher C, Quesada H ( 1999 ) On the roles of selection, mutation and drift in the evolution of mitochondrial DNA diversity in British Mytilus edulis (Mytilidae; Mollusca) populations. Biology Journal of the Linnean Society, 68, 195 – 213.en_US
dc.identifier.citedreferenceSterrer W ( 1986 ) Marine Fauna and Flora of Bermuda. Wiley and Sons, New York, NY.en_US
dc.identifier.citedreferenceStewart DT, Saavedra C, Stanwood RR, Ball AO, Zouros E ( 1995 ) Male and female mitochondrial DNA lineages in the blue mussel ( Mytilus edulis ) species group. Molecular Biology and Evolution, 12, 735 – 747.en_US
dc.identifier.citedreferenceSwofford DL ( 2003 ) paup*: Phylogenetic Analysis Using Parsimony (*and Other Methods), Version 4. Sinauer Associates, Sunderland, MA.en_US
dc.identifier.citedreferenceTajima F ( 1983 ) Evolutionary relationship of DNA sequences in finite populations. Genetics, 105, 437 – 460.en_US
dc.identifier.citedreferenceTajima F ( 1989 ) Statistical method for testing the neutral mutation hypothesis by DNA polymorphism. Genetics, 123, 585 – 595.en_US
dc.identifier.citedreferenceTamura K, Nei M ( 1993 ) Estimation of the number of nucleotide substitution in the control region of mitochondrial DNA in humans and chimpanzees. Molecular Biology and Evolution, 10, 512 – 526.en_US
dc.identifier.citedreferenceTempleton AR, Crandall KA, Sing CF ( 1992 ) A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping and DNA sequence data. III. Cladogram estimation. Genetics, 132, 619 – 633.en_US
dc.identifier.citedreferenceThompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG ( 1997 ) The clustal_x window interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Research, 25, 4876 – 4882.en_US
dc.identifier.citedreferenceWares JP ( 2002 ) Community genetics in the northwestern Atlantic intertidal. Molecular Ecology, 11, 1131 – 1144.en_US
dc.identifier.citedreferenceWares JP, Cunningham CW ( 2001 ) Phylogeography and historical ecology of the North Atlantic intertidal. Evolution, 55, 2455 – 2469.en_US
dc.identifier.citedreferenceWebb SD ( 1990 ) Historical biogeography. In: Ecosystems of Florida (eds Myers RI, Ewel JJ ), pp. 70 – 100. University of Central Florida Press, Orlando, FL.en_US
dc.identifier.citedreferenceWhite LR, McPherson BA, Stauffer JR ( 1996 ) Molecular genetic identification tools for the unionids of French Creek, Pennsylvania. Malacologia, 38, 181 – 202.en_US
dc.identifier.citedreferenceWilliams ST, Benzie JAH ( 1998 ) Evidence of a biogeographic break between populations of a high dispersal starfish: congruent regions within the Indo-West Pacific defined by color morphs, mtDNA, and allozyme data. Evolution, 52, 87 – 99.en_US
dc.identifier.citedreferenceWilliams D, Dunkerley D, DeDekker P, Kershaw P, Chappel M ( 1998 ) Quaternary Environments. Arnold, London.en_US
dc.identifier.citedreferenceXu Z, Guo X, Gaffney PM, Pierce JC ( 2001 ) Chromosomal location of the major ribosomal RNA genes in Crassostrea virginica and Crassostrea gigas. Veliger, 44, 79 – 83.en_US
dc.identifier.citedreferenceZouros E, Ball AO, Saaverda C, Freeman KR ( 1994 ) Mitochondrial DNA inheritance. Nature, 368, 818.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.