Abstract
The polychaete diversity of the Gulf of Mexico was examined using a comprehensive species database. The Gulf of Mexico was divided into four geographic regions and six depth classes; β-diversity between the 24 polygons was calculated with the Sørensen similarity index and analyzed using a cluster analysis and an ordination based on non-metric multidimensional scaling. Both analyses revealed a strong influence of depth on the polychaete assemblages. The polychaete fauna in the southeastern sector was the most distinctive among the four sectors. Each of the 835 polychaete species and subspecies was assigned to a class in the categories “mobility,” “feeding strategy,” and “feeding appendage” and the compositions of the categories throughout different depths were examined. The categories introduced by Fauchald and Jumars (Oceanogr Mar Biol Annu Rev 17:193–284, 1979) were amended and the suggested changes discussed. Each species was assigned to a biogeographical class based on their worldwide distributions. Ten percent of the polychaete species were endemic to the Gulf of Mexico. More than 40 % of the species were exclusively found in the Atlantic Ocean and the Gulf of Mexico, about one-third of the polychaetes had a wide distribution, and 15 % of all species were restricted to both coasts of the American continent. Below 200 m more than 30 % of the species were endemic. Thorough taxonomic research will be pivotal in fostering our understanding of the Gulf of Mexico polychaete fauna.
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Appeltans W, Ahyong ST, Anderson G, Angel MV, Artois T, Bailly N, Bamber R, Barber A, Bartsch I, Berta A, Błażewicz-Paszkowycz M, Bock P, Boxshall G, Boyko CB, Brandão SN, Bray RA, Bruce NL, Cairns SD, Chan TY, Cheng L, Collins AG, Cribb T, Curini-Galletti M, Dahdouh-Guebas F, Davie PJ, Dawson MN, De Clerck O, Decock W, De Grave S, de Voogd NJ, Domning DP, Emig CC, Erséus C, Eschmeyer W, Fauchald K, Fautin DG, Feist SW, Fransen CH, Furuya H, Garcia-Alvarez O, Gerken S, Gibson D, Gittenberger A, Gofas S, Gómez-Daglio L, Gordon DP, Guiry MD, Hernandez F, Hoeksema BW, Hopcroft RR, Jaume D, Kirk P, Koedam N, Koenemann S, Kolb JB, Kristensen RM, Kroh A, Lambert G, Lazarus DB, Lemaitre R, Longshaw M, Lowry J, Macpherson E, Madin LP, Mah C, Mapstone G, McLaughlin PA, Mees J, Meland K, Messing CG, Mills CE, Molodtsova TN, Mooi R, Neuhaus B, Ng PK, Nielsen C, Norenburg J, Opresko DM, Osawa M, Paulay G, Perrin W, Pilger JF, Poore GC, Pugh P, Read GB, Reimer JD, Rius M, Rocha RM, Saiz-Salinas JI, Scarabino V, Schierwater B, Schmidt-Rhaesa A, Schnabel KE, Schotte M, Schuchert P, Schwabe E, Segers H, Self-Sullivan C, Shenkar N, Siegel V, Sterrer W, Stöhr S, Swalla B, Tasker ML, Thuesen EV, Timm T, Todaro MA, Turon X, Tyler S, Uetz P, van der Land J, Vanhoorne B, van Ofwegen LP, van Soest RW, Vanaverbeke J, Walker-Smith G, Walter TC, Warren A, Williams GC, Wilson SP, Costello MJ (2012a) The magnitude of global marine species diversity. Curr Biol 22:2189–2202
Appeltans W, Bouchet P, Boxshall GA, De Broyer C, de Voogd NJ, Gordon DP, Hoeksema BW, Horton T, Kennedy M, Mees J, Poore GCB, Read G, Stöhr S, Walter TC, Costello MJ (eds) (2012b). World Register of Marine Species. http://www.marinespecies.org. Accessed 15 Jan 2013
Baco AR, Smith CR (2003) High species richness in deep-sea chemoautotrophic whale skeleton communities. Mar Ecol Prog Ser 260:109–114
Baco AR, Rowden AA, Levin LA, Smith CR, Bowden DA (2010) Initial characterization of cold seep faunal communities on the New Zealand Hikurangi margin. Mar Geol 272:251–259
Barroso R, Klautau M, Solé-Cava AM, Paiva PC (2010) Eurythoe complanata (Polychaeta: Amphinomidae), the ‘cosmopolitan’ fireworm, consists of at least three cryptic species. Mar Biol 157:69–80
Beesley PL, Ross GJB, Glasby CJ (eds) (2000) Polychaetes & allies: the southern synthesis. Fauna of Australia. Vol. 4A Polychaeta, Myzostomida, Pogonophora, Echiura, Sipuncula. CSIRO Publishing, Melbourne
Bhaud M (1998) The spreading potential of polychaete larvae does not predict adult distributions; consequences for conditions of recruitment. Hydrobiologia 375(376):35–47
Carr CM (2012) Polychaete diversity and distribution patterns in Canadian marine waters. Mar Biodiv 42:93–107
Castelli A, Bianchi CN, Cantone G, Çinar ME, Gambi MC, Giangrande A, Iraci Sareri D, Lanera P, Licciano M, Musco L, Sanfilippo R, Simonini R (2008) Annelida Polychaeta. Biol Mar Mediterr 15(suppl):323–373
Clarke KR, Gorley RN (2006) PRIMER v6: user manual/tutorial. PRIMER-E, Plymouth
Coates AG, Obando JA (1996) The geological evolution of the Central American isthmus. In: Jackson JBC, Budd EF, Coates AG (eds) Evolution and environment in tropical America. The University of Chicago Press, Chicago, pp 21–56
Conway Morris S, Peel JS (2008) The earliest annelids: lower Cambrian polychaetes from the Sirius Passet Lagerstätte, Peary Land, North Greenland. Acta Palaeontol Pol 53:137–148
Dauer DM, Maybury CA, Ewing RM (1981) Feeding behavior and general ecology of several spionid polychaetes from the Chesapeake Bay. J Exp Mar Biol Ecol 54:21–38
Dauvin JC, Bachelet G, Bellan G (2006) Biodiversity and biogeographic relationships of the polychaete fauna in French Atlantic and Mediterranean waters. Sci Mar 70S3:259–267
Desbruyères D, Segonzac M, Bright M (2006) Handbook of deep-sea hydrothermal vent fauna. Denisia 18:1–544
Fauchald K (1982) Revision of Onuphis, Nothria, and Paradiopatra (Polychaeta: Onuphidae) based upon type material. Smithson Contrib Zool 356:1–109
Fauchald K (1984) Polychaete distribution patterns, or: can animals with Palaeozoic cousins show largescale geographical patterns. In: Hutchings PA (ed) Proceedings of the first international polychaete conference. The Linnean Society of New South Wales, Sydney, pp 1–6
Fauchald K (1992) A review of the genus Eunice (Polychaeta: Eunicidae) based upon type material. Smithson Contrib Zool 523:1–422
Fauchald K, Jumars PA (1979) The diet of worms: a study of polychaete feeding guilds. Oceanogr Mar Biol Annu Rev 17:193–284
Fauchald K, Granados-Barba A, Solís-Weiss V (2009) Polychaeta (Annelida) of the Gulf of Mexico. In: Felder DL, Camp DK (eds) Gulf of Mexico origin, waters, and biota: volume I, biodiversity. Texas A&M University Press, College Station, pp 751–788
Felder DL, Camp DK (2009) Gulf of Mexico origin, waters, and biota: volume I, biodiversity. Texas A&M University Press, College Station
Fiege D, Ramey PA, Ebbe B (2010) Diversity and distributional patterns of Polychaeta in the deep South Atlantic. Deep Sea Res I 57:1329–1344
Galtsoff PS (ed) (1954) Gulf of Mexico, its origin, waters and marine life. Fishery Bulletin 89. Fishery Bulletin of the Fish and Wildlife Service, volume 55. United States Government Printing Office, Washington
Gaston GR, McLelland JA, Heard RW (1992) Feeding biology, distribution, and ecology of two species of benthic polychaetes: Paraonis fulgens and Paraonis pygoenigmatica (Polychaeta: Paraonidae). Gulf Res Rep 8:395–399
Glasby CJ, Alvarez B (1999) Distribution patterns and biogeographic analysis of Austral Polychaeta (Annelida). J Biogeogr 26:507–533
Glasby CJ, Watson C (2001) A new genus and species of Syllidae (Annelida: Polychaeta) commensal with octocorals. Beagle 17:43–51
Glover A, Paterson G, Bett B, Gage J, Sibuet M, Sheader M, Hawkins L (2001) Patterns in polychaete abundance and diversity from the Madeira Abyssal Plain, northeast Atlantic. Deep Sea Res I 48:217–236
Grassle J, Grassle JF (1976) Sibling species in the marine pollution indicator Capitella (Polychaeta). Science 192:567–569
Guillou M, Hily C (1983) Dynamics and biological cycle of a Melinna palmata (Ampharetidae) population during the recolonisation of a dredged area in the vicinity of the harbour of Brest (France). Mar Biol 73:43–50
Hartman O (1951) The littoral marine annelids of the Gulf of Mexico. Publ Inst Mar Sci 2:7–124
Hartman O (1954) Polychaetous annelids of the Gulf of Mexico. In: Galtsoff PS (ed) Gulf of Mexico, its origin, waters and marine life. Fishery Bulletin 89. Fishery Bulletin of the Fish and Wildlife Service, volume 55. United States Government Printing Office, Washington, pp 413–417
Hedgpeth JW (1953) An introduction to the zoogeography of the northwestern Gulf of Mexico with reference to the invertebrate fauna. Publ Inst Mar Sci 3:107–224
Imajima M, Reuscher MG, Fiege D (2013) Ampharetidae (Annelida: Polychaeta) from Japan. Part II: Genera with elevated and modified notopodia. Zootaxa 3647:137–166
Knox GA (1957) The distribution of polychaetes in the Indo-Pacific. Proc 8th Pac Sci Congr 3:403–411
Kruse I, Strasser M, Thiermann F (2004) The role of ecological divergence in speciation between intertidal and subtidal Scoloplos armiger (Polychaeta, Orbiniidae). J Sea Res 51:53–62
Mareano (2013) Mareano. Samler kunnskap om havet. http://www.mareano.no/bilder/videoer. Accessed 12 Feb 2013
Martin D, Marin I, Britayev TA (2008) Features of the first known association between Syllidae (Annelida, Polychaeta) and crustaceans. Org Divers Evol 8:279–281
Montiel San Martín A, Gerdes D, Arntz WE (2005) Distributional patterns of shallow-water polychaetes in the Magellan region: a zoogeographical and ecological synopsis. Sci Mar 69:123–133
Moretzsohn F, Brenner J, Michaud P, Tunnell JW, Shirley T (2011) Biodiversity of the Gulf of Mexico Database (BioGoMx). Version 1.0. Harte Research Institute for Gulf of Mexico Studies (HRI). Texas A&M University-Corpus Christi (TAMUCC), Corpus Christi, http://www.gulfbase.org/biogomx/biosearch.php. Accessed 26 Jul 2011
OBIS (2013) Ocean Biogeographic Information System. http://www.iobis.org. Accessed 25 Jan 2013
Paterson GLJ, Glover AG, Barrio Froján CRS, Whitaker A, Budaeva N, Chimonides J, Doner S (2009) A census of abyssal polychaetes. Deep Sea Res II 56:1739–1746
Pawlik JR (1983) A sponge-eating worm from Bermuda: Branchiosyllis oculata (Polychaeta, Syllidae). Mar Ecol 4:65–79
Pettibone MH (1953) Some scale-bearing polychaetes of Puget Sound and adjacent waters. University of Washington Press, Seattle
Pettibone MH (1984) A new scale-worm commensal with deep-sea mussels on the Galapagos hydrothermal vent (Polychaeta: Polynoidae). Proc Biol Soc Wash 97:226–239
Read G, Fauchald K (eds) (2012) World Polychaeta database. http://www.marinespecies.org/polychaeta. Accessed 15 Jan 2013
Reish DJ (1957) The relationship of the polychaetous annelid Capitella capitata (Fabricius), to waste discharges of biological origin. In: Tarzwell CM (ed) Biological problems in water pollution. United States Public Health Services, Washington, pp 195–200
Rubinoff I (1968) Central American sea-level canal: possible biological effects. Science 161:857–861
San Martín G (1990) Eusyllinae (Syllidae, Polychaeta) from Cuba and Gulf of Mexico. Bull Mar Sci 46:560–619
San Martín G (1991a) Syllinae (Polychaeta: Syllidae) from Cuba and the Gulf of Mexico. Bull Mar Sci 48:227–235
San Martín G (1991b) Grubeosyllis and Exogone (Exogoninae, Syllidae, Polychaeta) from Cuba, the Gulf of Mexico, Florida and Puerto Rico, with a revision of Exogone. Bull Mar Sci 49:715–740
San Martín G (1992) Syllis Savigny in Lamarck, 1818 (Polychaeta: Syllidae: Syllinae) from Cuba, the Gulf of Mexico, Florida and North Carolina, with a revision of several species described by Verrill. Bull Mar Sci 51:167–196
Scheltema RS (1986) Long-distance dispersal by planktonic larvae of shoal-water benthic invertebrates among central Pacific islands. Bull Mar Sci 39:241–256
Schüller M, Ebbe B (2007) Global distributional patterns of selected deep-sea Polychaeta (Annelida) from the Southern Ocean. Deep Sea Res II 54:1737–1751
Schüller M, Ebbe B, Wägele J-W (2009) Community structure and diversity of polychaetes (Annelida) in the deep Weddell Sea (Southern Ocean) and adjacent basins. Mar Biodiv 39:95–108
Schulze SR, Rice SA, Simon JL, Karl SA (2000) Evolution of poecilogony and the biogeography of North American populations of the polychaete Streblospio. Evolution 54:1247–1259
Sørensen T (1948) A method of establishing groups of equal amplitude in plant sociology based on similarity of species and its application to analyses of the vegetation on Danish commons. Dan Vidensk Selsk Biol Skr 5:1–34
Spivey HR (1981) Origins, distribution, and zoogeographic affinities of the Cirripedia (Crustacea) of the Gulf of Mexico. J Biogeogr 8:153–176
Struck TH, Paul C, Hill N, Hartmann S, Hösel C, Kube M, Lieb B, Meyer A, Tiedemann R, Purschke G, Bleidorn C (2011) Phylogenomic analyses unravel annelid evolution. Nature 471:95–98
Uebelacker JM, Johnson PG (eds) (1984) Taxonomic guide to the polychaetes of the northern Gulf of Mexico. Final Report to the Minerals Management Service, contract 14-12-001-29091. Barry A. Vittor & Associates, Mobile, 7 volumes
Wehe T (2006) Revision of the scale worms (Polychaeta: Aphroditoidea) occurring in the seas surrounding the Arabian Peninsula. Part I: Polynoidae. Fauna Arab 22:23–197
Wehe T (2007) Revision of the scale worms (Polychaeta: Aphroditoidea) occurring in the seas surrounding the Arabian Peninsula. Part II: Sigalionidae. Fauna Arab 23:41–124
Wehe T, Fiege D (2002) Annotated checklist of the polychaete species of the seas surrounding the Arabian Peninsula: Red Sea, Gulf of Aden, Arabian Sea, Gulf of Oman, Arabian Gulf. Fauna Arab 19:7–238
Wicksten MK, Packard JM (2005) A qualitative zoogeographic analysis of decapod crustaceans of the continental slopes and abyssal plain of the Gulf of Mexico. Deep Sea Res I 52:1745–1765
Zrzavý J, Říha P, Piálek L, Janouškovec J (2009) Phylogeny of Annelida (Lophotrochozoa): total-evidence analysis of morphology and six genes. BMC Evol Biol 9:189. doi:10.1186/1471-2148-9-189
Acknowledgments
Drs. John W. “Wes” Tunnell, Frank Pezold, Kim Withers (all Texas A&M University-Corpus Christi), and Anja Schulze (Texas A&M University at Galveston) improved the quality of the manuscript through meticulous reviews. Dr. Fabio Moretzsohn (Texas A&M University-Corpus Christi) is thanked for his insightful explanations on details of the BioGoMx database and the “Bulletin 89.” The College of Science and Engineering at Texas A&M University–Corpus Christi is thanked for supporting M.G.R. through teaching assistantships from fall 2008 to spring 2011 and through summer research scholarships in the years 2010–2013. Dr. Paul Montagna (Texas A&M University–Corpus Christi) is thanked for his support of M.G.R. through a research assistantship between fall 2011 and fall 2013.
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Table S1
Geographical and bathymetrical records of Gulf of Mexico polychaetes, along with data on their ecological guilds and distribution. NW northwestern sector, NE northeastern sector, SW southwestern sector, SE southeastern sector; D1–6 depth classes 1–6 as defined in “Materials and methods”; M mobility, including the categories M mobile, D discretely mobile, S sessile; F feeding strategy, including SS subsurface deposit feeder, SD surface deposit feeder, DS deposit feeder with facultative suspension feeding, SU suspension feeder, CV carnivore, OV omnivore, SY host of symbionts; A feeding appendage, including UP unarmed pharynx, PA palps, PP unarmed pharynx and palps, AP armed pharynx, R radula like pharynx, TE tentacles, FI filtering structure, LI lips, LT lips and tentacles, PU pumping device, NP not present; D distribution class, including EN endemic, NW West Atlantic, north of the Gulf of Mexico, SW West Atlantic, south of the Gulf of Mexico, WA West Atlantic, north and south of the Gulf of Mexico, AT Pan-Atlantic, AM Pan-American, HA holarctic, WD widely distributed. (PDF 2032 kb)
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Reuscher, M.G., Shirley, T.C. Diversity, distribution, and zoogeography of benthic polychaetes in the Gulf of Mexico. Mar Biodiv 44, 519–532 (2014). https://doi.org/10.1007/s12526-014-0222-7
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DOI: https://doi.org/10.1007/s12526-014-0222-7