Macrorhynchia philippina Kirchenpauer, 1872
publication ID |
https://doi.org/10.11646/zootaxa.4689.1.1 |
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https://treatment.plazi.org/id/9E4CE23A-FFAD-F123-FF03-64CAFE53286C |
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Plazi (2019-10-25 12:55:46, last updated 2024-11-26 14:23:24) |
scientific name |
Macrorhynchia philippina Kirchenpauer, 1872 |
status |
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Macrorhynchia philippina Kirchenpauer, 1872 View in CoL
Fig. 22f View FIGURE 22
Macrorhynchia philippina Kirchenpauer, 1872: 19 View in CoL .
Aglaophenia philippina Kirchenpauer, 1872: 45 View in CoL , text-fig. p. 17; pl. 1, fig. 26; pl. 2, figs. 26a-b; pl. 7, fig. 26.
Lytocarpus philippinnus .— Wallace, 1909: 137 [incorrect subsequent spelling].
Type locality. Philippines: Manila ( Kirchenpauer 1872: 45, as Aglaophenia philippina ) .
Material examined. Sanibel Island, beach at Lighthouse Point, 26°26’57”N, 82°01’07”W, detached and in water along shore, 21 February 2013, one colony, 18 cm high, without phylactocarps, coll. D. Calder, ROMIZ B4404.— Sanibel Island , beach at Lighthouse Point, detached and stranded in tidepool, 30 March 2013, one colony, 8 cm high, without phylactocarps, coll. D. Calder, ROMIZ B4405 .— Sanibel Island , beach at Lighthouse Point, 26°26’59”N, 82°01’03”W, on detached shell fragments at water’s edge, 13 March 2018, 20° C, 33.5‰, one colony, 15 cm high, with gonophores, coll. D. Calder, ROMIZ B4406 GoogleMaps .
Remarks. Macrorhynchia philippina , considered distinctive in traditional taxonomy largely on the basis of hydrothecal characters ( Fig. 22f View FIGURE 22 ), is thought to be essentially circumglobal in warm neritic waters ( Calder 2013). Molecular work on this hydroid has been limited, but thus far it seems to support the likelihood of a wide geographic range. Moura et al. (2012) discovered the same 16S genotype in hydroids identified as this species from two widely separated locations in the Atlantic Ocean ( Brazil and Madeira). In another analysis, the phylogram of Postaire et al. (2016), shows little intraspecific divergence in specimens assigned to this species from Moorea in the tropical western Pacific, from Juan de Nova Island in the Indian Ocean, and from the two Atlantic populations mentioned above.
Several records of M. philippina from the western North Atlantic require comment. Although the species is known to occur in Bermuda (Calder 1997), Congdon’s (1907) record of it from there (as Lytocarpus philippinus ) is based, at least in part, on a misidentification ( Bale 1919: 352; Stechow 1920: 44; Calder 1997: 68). As evidence of this, an illustration of the species ( Congdon 1907, fig. 37) portrays M. allmani ( Nutting, 1900) instead. It is likely that specimens collected nearshore were M. philippina , while those from Challenger Bank were M. allmani . Records of M. philippina from Bermuda by Smallwood (1910) and Bennitt (1922) are somewhat uncertain given earlier confusion over the species in the area. Nutting (1900) reported M. philippina from Panama, but he failed to indicate whether the hydroids he examined were from the Atlantic or Pacific coast of that country.
More detailed accounts of this species in the western North Atlantic are given elsewhere (Calder 1997, 2013). An extensive synonymy list under M. philippina appears in Ansín Agís et al. (2001). Gonophores are liberated as short-lived medusoids ( Gravier 1970; Migotto 1996; Bourmaud & Gravier-Bonnet 2004; Galea 2018).
Reported distribution. Gulf coast of Florida. Dry Tortugas ( Wallace 1909: 137, as Lytocarpus philippinnus ).
Elsewhere in western North Atlantic. Jamaica ( Nutting 1900: 123, as Lytocarpus philippinus ).—? Panama ( Nutting 1900: 123, as Lytocarpus philippinus ).— Bermuda: shore areas ( Congdon 1907: 484 [part], as Lytocarpus philippinus ).— Bermuda: Fairyland Point ( Smallwood 1910, as Lytocarpus philippinus ).— USA: North Carolina, Bogue Sound, 10 ft (3 m) + Shackleford Banks, shallow water ( Fraser 1912b: 379, as Lytocarpus philippinus ).—? Bermuda: Somerset Bridge ( Bennitt 1922: 254, as Lytocarpus philippinus ).— USA: Florida, Biscayne Bay ( Weiss 1948: 158, as Lytocarpus philippinus ).— USA: unstated location: on buoys ( Woods Hole Oceanographic Institution 1952: 187, as Lytocarpus philippinus ).— USA: Florida, Biscayne Bay, Soldier Key ( Voss & Voss 1955: 223, as Lytocarpus filippinus ).— USA: Mississippi, Mississippi Sound ( Fincher 1955: 92, as Lytocarpus philippinus ).— Sint Maarten: Great Bay, NE shore, tidal zone ( Van Gemerden-Hoogeveen 1965: 74, as Lytocarpus philippinus ).— Venezuela: Puerto Cabello ( Vervoort 1968: 88, as Lytocarpus philippinus ).— Colombia; Santa Marta area ( Wedler 1975: 333, as Lytocarpus philippinus ).— Mexico, Arrowsmith Bank, 21°07’N, 86°21’W, 49–55 m ( Bogle 1975: 61).— USA: Florida, Sebastian Inlet, 1.0– 1.5 m ( Clark & Goetzfried 1976: 477, as Lytocarpus sp.).— USA: South Carolina, Bulls Bay, 5 m + Prices Creek, 8 m + Capers Inlet, 3 m + Beaufort River, 6 m + Chechessee River, 9 m ( Calder & Hester 1978: 91, as Lytocarpus philippinus ; Calder 1983: 23).— Colombia: Bahia de Cartagena area, Bocachica + Obelisco + Chamba + Faro de Salmedina ( Flórez González 1983: 123, as Lytocarpus philippinus ).— Colombia: Santa Marta area ( Bandel & Wedler 1987: 38, as Lytocarpus philippinus ).— Bermuda: various localities ( Calder 1986: 139).— USA: Florida, artificial reef off Boca Raton ( Cummings 1994: 1208, as Lytocarpus philippinus ).— Bermuda: Flatts Inlet, 2 m + Harrington Sound, entrance of Cripplegate Cave, 1 m (Calder 1997: 66).— USA: Florida, Biscayne Bay ( Jones 2002: 218, as Macrorynchia philippina ).— Panama: Bocas del Toro area, Swan’s Key, 09°27’12.2”N, 82°18’01.8”W, 1–4 m ( Calder & Kirkendale 2005: 483).—French Lesser Antilles: Guadeloupe, Grande-Terre, Les Arches, 16°27.529’N, 61°32.021’W, 17 m + L’Oeil, 16°26.782’N, 61°32.405’W, 12–17 m + Pointe d’Antigues 16°26.251’N, 61°32.523’W ( Galea 2010: 34).—French Lesser Antilles: Les Saintes, Terre-de-Haut, La Baleine du Large, 15°52.820’N, 61°35.226’W, 20 m ( Galea 2010: 34).— Cuba: Ciego de Ávila, Cayo Guillermo, 5 m ( Varela 2012: 6).— USA: Florida, Bethel Shoal off Vero Beach, 27°42.6’N, 80°06.8’W, 24 m ( Calder 2013: 52).—French Lesser Antilles: Martinique ( Galea 2013: 50).—Caribbean Sea ( Wedler 2017b: 152, figs. 185A, B, 186, 187).
Ansin Agis, J., Ramil, F. & Vervoort, W. (2001) Atlantic Leptolida (Hydrozoa, Cnidaria) of the families Aglaopheniidae, Halopterididae, Kirchenpaueriidae and Plumulariidae collected during the CANCAP and Mauritania-II expeditions of the National Museum of Natural History, Leiden, the Netherlands. Zoologische Verhandelingen, 333, 1 - 268.
Bale, W. M. (1919) Further notes on Australian hydroids - IV. Proceedings of the Royal Society of Victoria, New Series, 31, 327 - 361.
Bandel, K. & Wedler, E. (1987) Hydroid, amphineuran and gastropod zonation in the littoral of the Caribbean Sea, Colombia. Senckenbergiana Maritima, 19, 1 - 129.
Bennitt, R. (1922) Additions to the hydroid fauna of the Bermudas. Proceedings of the American Academy of Arts and Sciences, 57, 241 - 259. https: // doi. org / 10.2307 / 20025913
Bogle, M. A. (1975) A review and preliminary revision of the Aglaopheniinae (Hydroida: Plumulariidae) of the tropical western Atlantic. M. S. Thesis, University of Miami, Coral Gables, 307 pp.
Bourmaud, C. & Gravier-Bonnet, N. (2004) Medusoid release and spawning of Macrorynchia philippina Kirchenpauer 1872 (Cnidaria, Hydrozoa, Aglaopheniidae). Hydrobiologia, 530 - 531, 365 - 372. https: // doi. org / 10.1007 / s 10750 - 004 - 2665 - 5
Calder, D. R. & Hester, B. S. (1978) Phylum Cnidaria. In: Zingmark, R. G. (Ed.), An annotated checklist of the biota of the coastal zone of South Carolina. University of South Carolina Press, Columbia, pp. 87 - 93.
Calder, D. R. (1983) Hydroida from estuaries of South Carolina, USA: families Sertulariidae and Plumulariidae. Proceedings of the Biological Society of Washington, 96, 7 - 28. https: // doi. org / 10.2307 / 1351954
Calder, D. R. (1986) Class Hydrozoa. In: Sterrer, W. (Ed.), Marine fauna and flora of Bermuda: a systematic guide to the identification of marine organisms. Wiley-Interscience, New York, pp. 127 - 155.
Calder, D. R. & Kirkendale, L. (2005) Hydroids (Cnidaria, Hydrozoa) from shallow-water environments along the Caribbean Coast of Panama. Caribbean Journal of Science, 41, 476 - 491.
Calder, D. R. (2013) Some shallow-water hydroids (Cnidaria: Hydrozoa) from the central east coast of Florida, USA. Zootaxa, 3648 (1), 1 - 72. https: // doi. org / 10.11646 / zootaxa. 3648.1.1
Clark, K. B. & Goetzfried, A. (1976) Lomanotus stauberi, a new dendronotacean nudibranch from central Florida (Mollusca: Opisthobranchia). Bulletin of Marine Science, 26, 474 - 478.
Congdon, E. D. (1907) The hydroids of Bermuda. Proceedings of the American Academy of Arts and Sciences, 42, 463 - 485. https: // doi. org / 10.2307 / 20022242
Cummings, S. L. (1994) Colonization of a nearshore artificial reef at Boca Raton (Palm Beach County), Florida. Bulletin of Marine Science, 55, 1193 - 1215.
Fincher, J. A. (1955) Notes on the hydroids of the Mississippi Sound. Journal of the Alabama Academy of Science, 27, 91 - 92. [abstract]
Florez Gonzalez, L. (1983) Inventario preliminar de la fauna hydroide de la Bahia de Cartagena y areas adyacentes. Boletin del Museo del Mar, Bogota, 11, 112 - 140.
Fraser, C. M. (1912 b) Some hydroids of Beaufort, North Carolina. Bulletin of the United States Bureau of Fisheries, 30, 339 - 387.
Galea, H. R. (2010) Additional shallow-water thecate hydroids (Cnidaria: Hydrozoa) from Guadeloupe and Les Saintes, French Lesser Antilles. Zootaxa, 2570 (1), 1 - 40. https: // doi. org / 10.11646 / zootaxa. 2570.1.1
Galea, H. R. (2013) New additions to the shallow-water hydroids (Cnidaria: Hydrozoa) of the French Lesser Antilles: Martinique. Zootaxa, 3686 (1), 1 - 50. https: // doi. org / 10.11646 / zootaxa. 3686.1.1
Galea, H. R. (2018) A swimming medusoid gonophore in the life cycle of Ventromma halecioides (Alder, 1859) (Hydrozoa: Leptothecata: Kirchenpaueriidae). Revue Suisse de Zoologie, 125, 137 - 147.
Gravier, N. (1970) Liberation de medusoides par Macrorhynchia philippina Kirchenpauer, 1872 (Hydroida, Plumulariidae). Recueil des Travaux de la Station Marine d'Endoume, Fascicle Hors Serie Supplement, 10, 253 - 257.
Jones, T. (2002) Biology and ecology of athecate hydroids in Biscayne Bay, Florida: potential use as bioindicators. Ph. D. Dissertation, University of Miami, Coral Gables, 287 pp.
Kirchenpauer, G. H. (1872) Ueber die Hydroidenfamilie Plumularidae, einzelne Gruppen derselben und ihre Fruchtbehalter. I. Aglaophenia Lx. Abhandlungen aus dem Gebiete der Naturwissenschaften herausgegeben von dem Naturwissenschaftlichen Verein in Hamburg, 5 (3), 1 - 52.
Migotto, A. E. (1996) Benthic shallow-water hydroids (Cnidaria, Hydrozoa) of the coast of Sao Sebastiao, Brazil, including a checklist of Brazilian hydroids. Zoologische Verhandelingen, 306, 1 - 125.
Moura, C. J., Cunha, M. R., Porteiro, F. M. & Rogers, A. D. (2012) A molecular phylogenetic appraisal of the systematics of the Aglaopheniidae (Cnidaria: Hydrozoa, Leptothecata) from the north-east Atlantic and west Mediterranean. Zoological Journal of the Linnean Society, 164, 717 - 727. https: // doi. org / 10.1111 / j. 1096 - 3642.2011.00784. x
Nutting, C. C. (1900) American hydroids. Part I. The Plumularidae. Smithsonian Institution, United States National Museum Special Bulletin, 4 (1), 1 - 285.
Postaire, B., Magalon, H., Bourmaud, C. A. - F., Gravier-Bonnet, N. & Bruggemann, J. H. (2016) Phylogenetic relationships within Aglaopheniidae (Cnidaria, Hydrozoa) reveal unexpected generic diversity. Zoologica Scripta, 45, 103 - 114. https: // doi. org / 10.1111 / zsc. 12135
Smallwood, W. M. (1910) Notes on the hydroids and nudibranchs of Bermuda. Proceedings of the Zoological Society of London, 1910, 137 - 145. https: // doi. org / 10.1111 / j. 1096 - 3642.1910. tb 01888. x
Stechow, E. (1920) Neue Ergebnisse auf dem Gebiete der Hydroidenforschung. Sitzungsberichte der Gesellschaft fur Morphologie und Physiologie in Munchen, 31, 9 - 45.
Van Gemerden-Hoogeveen, G. C. H. (1965) Hydroids of the Caribbean: Sertulariidae, Plumulariidae and Aglaopheniidae. Studies on the Fauna of Curacao and other Caribbean Islands: No. 84. Studies on the Fauna of Curacao, 22, 1 - 45.
Varela, C. (2012) Registros nuevos de hidrozoos (Cnidaria: Hydroidomedusae) para Cuba, con la descripcion de una especie nueva. Solenodon, 10, 1 - 7. https: // doi. org / 10.33800 / nc. v 0 i 5.60
Vervoort, W. (1968) Report on a collection of Hydroida from the Caribbean region, including an annotated checklist of Caribbean hydroids. Zoologische Verhandelingen, 92, 1 - 124.
Voss, G. L. & Voss, N. A. (1955) An ecological survey of Soldier Key, Biscayne Bay, Florida. Bulletin of Marine Science of the Gulf and Caribbean, 5, 203 - 229.
Wallace, W. S. (1909) A collection of hydroids made at the Tortugas, during May, June, and July, 1908. Carnegie Institution of Washington, Year Book, 7, 136 - 138.
Wedler, E. (1975) Okologische Untersuchungen an Hydroiden des Felslitorals von Santa Marta (Kolumbien). Helgolander Wissenschaftliche Meeresuntersuchungen, 27, 324 - 363. https: // doi. org / 10.1007 / BF 01611700
Wedler, E. (2017 b) Hidroides del Mar Caribe con enfasis en la region de Santa Marta, Colombia. Instituto de Investigaciones Marinas y Costeras-INVEMAR. Serie de Publicaciones Generales del INVEMAR # 94, Santa Marta, Colombia, 200 pp.
Weiss, C. M. (1948) The seasonal occurrence of sedentary marine organisms in Biscayne Bay, Florida. Ecology, 29, 153 - 172. https: // doi. org / 10.2307 / 1932811
Woods Hole Oceanographic Institution (1952) Marine fouling and its prevention. United States Naval Institute, Annapolis, Maryland, 388 pp.
FIGURE 22. a, Aglaophenia dubia: part of a hydrocladium with two hydrothecae, Southwest Florida Shelf, ROMIZ B2147. Scale equals 0.1 mm. b, Aglaophenia latecarinata: part of a hydrocladium with three hydrothecae, Fort Myers Beach, ROMIZ B4402. Scale equals 0.1 mm. c, Gymnangium sinuosum: part of a hydrocladium with one hydrotheca, Southwest Florida Shelf, ROMIZ B2203. Scale equals 0.1 mm. d, Lytocarpia tridentata: part of a hydrocladium with two hydrothecae, Florida Keys, Bahia Honda Channel, ROMIZ B3806. Scale equals 0.1 mm. e, Macrorhynchia allmani: part of a hydrocladium with two hydrothecae, Southwest Florida Shelf, ROMIZ B2187. Scale equals 0.1 mm. f, Macrorhynchia philippina: part of a hydrocladium with two hydrothecae, Sanibel Island, ROMIZ B4405. Scale equals 0.1 mm.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
Kingdom |
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Phylum |
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Class |
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SubClass |
Hydroidolina |
Order |
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Family |
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Genus |
Macrorhynchia philippina Kirchenpauer, 1872
Calder, Dale R. 2019 |
Lytocarpus philippinnus
Wallace, W. S. 1909: 137 |
Macrorhynchia philippina
Kirchenpauer, G. H. 1872: 19 |
Aglaophenia philippina
Kirchenpauer, G. H. 1872: 45 |
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