Watersipora subatra Vieira & Jones & Taylor 2014, n. stat.
- 1. Centro de Biologia Marinha, Universidade de São Paulo, São Sebastião, São Paulo, Brazil. E-mail: leandromanzoni @ hotmail. com Departamento de Zoologia, Centro de Ciências Biológicas, Universidade Federal de Pernambuco, Recife, Pernambuco, Brazil Department of Life Sciences, Natural History Museum, London, UK. E-mail: m. spencer-jones @ nhm. ac. uk
- 2. Department of Earth Sciences, Natural History Museum, London, UK. E-mail: p. taylor @ nhm. ac. uk
Description
Watersipora subatra (Ortmann, 1890) n. stat.
(Figs 39–53, 66, 69; Table 3)
Schizoporella aterrima var. subatra Ortmann, 1890: 49 [Japan].
? Watersipora cucullata var. watersi Mawatari, 1952: 12 (part), fig. 1G [Japan].
Dakaria subovoidea: Harmer 1957: p. 1022 (part), pl. 49, figs 11–12, 14 [Indonesia].
? Cellepora subovoidea d’Orbigny, 1852: 402 [Red Sea; nomen dubium].
Watersipora subtorquata: Ryland 1974: 345, fig. 3C [Low Island]. Non Cellepora subtorquata d’Orbigny, 1852: 399 [Brazil]. “ Watersipora subovoidea ” fide Harmer: Soule & Soule 1975: 308 (part), pl. 3, fig. 6 [Australia].
“ Watersipora subovoidea ” fide Harmer: Winston & Heimberg, 1986: 15, figs 35–37 [Komodo].
Watersipora subtorquata: Gordon 1989: 40, pl. 20, B–H [New Zealand].
Watersipora subtorquata: Gordon & Mawatari, 1992: 30 [New Zealand].
Watersipora subtorquata: Ryland et al. 2009: 55, figs 3, 4A, C, E, F [Australia, Bay of Biscay and English Channel]. Watersipora subtorquata: Kelso & Wyse-Jackson 2012: 2010, fig. 1 [Ireland].
Watersipora subtorquata: Kuhlenkamp & Kind 2013: 3, figs 1B, C, 2A–F [North Sea: Helgoland].
Material examined. Holotype: MZS 002, Ortmann Collection, Sagami Bay, Japan, 50–100 fm (15–30 m), 1882. Other material: NHMUK 1922.10.8.3, dry slide, Schizoporella cucullata, sea level, Misaki, Japan, No. 1, Insole coll. NHMUK 1929.12.31.1, dry slide, Watersipora atrofusca, Australia, MacGillivray coll. NHMUK 2005.5.26.19, dry, Watersipora subtorquata, scraped from hull of Seasprite, Leigh Wharf / Marina, North Island, New Zealand, 6 October 2004, K. Tilbrook coll. NHMUK 2007.12.14.9, balsam slide, Watersipora subtorquata, J.S. Ryland det., Low Islands, Great Barrier Reef, July 1974, J.S. Ryland coll. NHMUK 2007.12.14.10, balsam slide, Watersipora subtorquata, J.S. Ryland det., Low Islands, Great Barrier Reef, July 1974, J.S. Ryland coll. NHMUK 2007.12.14.12, balsam slide, Watersipora subtorquata, J.S. Ryland don., on shell, Bay of Arcachon, August 2003, Hans de Blauwe coll. NHMUK 2007.12.14.14, balsam slide, Watersipora subtorquata, J.S. Ryland don., St-Jacut-sur-la-Mer, April 2005, Hans de Blauwe coll. NHMUK 2007.12.14.15, balsam slide, Watersipora subtorquata, J.S. Ryland don., St-Jacut-sur-la-Mer, April 2005, Hans de Blauwe coll. NHMUK 2007.12.14.16, balsam slide, Watersipora subtorquata, J.S. Ryland don., Guersey, 2007, R. Lord coll. NHMUK 2007.12.14.17, balsam slide, Watersipora subtorquata, J.S. Ryland don., Guersey, 2007, R. Lord coll. NHMUK 2007.12.14.18, balsam slide, Watersipora subtorquata, J.S. Ryland don., Guersey, 2007, R. Lord coll. NHMUK 2010.12.1.2, dry, Watersipora sp., Point Loma, Marina, San Diego, California, USA, September 2010. P.D. Taylor & B. Okamura coll. NHMUK 2010.6.30.7, dry and dry slide, Long Beach, Los Angeles, USA. NHMUK 2012.6.30.6, dry slide [part of NHMUK 2005.5.26.19], Watersipora subtorquata, scraped from hull of Seasprite, hauled out Leigh Wharf / Marina, North Island, New Zealand, 6 October 2004, K. Tilbrook coll.
Description. Colonies encrusting, multiserial, uni- to multilamellar; sometimes erect, foliaceous and bilamellar; colour in life variable, from orange to brownish-purple or greyish to black. Zooids subrectangular to hexagonal, about twice as long as wide, separated by slightly raised lateral walls. Frontal shield slightly convex, with numerous round pseudopores about 25 µm diameter; two large latero-oral intrazooidal septula near lateral zooidal margin, proximolateral to orifice, each with 3–8 (often 5) small pores. Frontal shield obscured by translucent cuticle. Orifice large, subcircular to oval, slightly wider than long, with broad, well-defined proximal, U-shaped sinus; orificial rim thin, sometimes slightly raised; narrow bar-shaped condyles, sometimes inconspicuous. Operculum with broad, biconcave proximal band, without lucidae. Avicularia absent. Ooecia absent.
Remarks. Ortmann (1890) described and figured Schizoporella aterrima from Japan, including the new variety subatra without drawings or description. Ryland et al. (2009) noted that Schizoporella aterrima Ortmann, 1890 is unrecognizable and that the description given by Mawatari (1952) for Watersipora cucullata var. watersi, another species reported from Japan, may include at least two species. One of us (MSJ) has examined Ortmann’s specimens deposited at the Musée zoologique de la Ville de Strasbourg, concluding that they represent two species, Watersipora aterrima (MZS 003; Figs 35–38; Table 3) and Watersipora subatra (MZS 002; Fig. 39–42; Table 3). Watersipora aterrima is distinguished from W. subatra by having a smaller orifice, narrower sinus and smaller frontal pseudopores.
Mawatari (1952) introduced variety watersi for specimens with distinctive opercula. His notes on this new variety are based on specimens from Japan, and two others recorded by Waters (1909) from Naples and by Hastings (1930) from Cape Verde. Unfortunately, Mawatari’s specimens from Japan assigned to W. cucullata var. watersi could not be located, but part of his description and figures resembles W. subatra and may refer to this species. We have assigned the Cape Verde and Naples specimens to a different species, Watersipora souleoroum n. sp. (see below).
Comparisons between specimens from New Zealand (Figs 43–47), California (Fig 48–53) and Britain (some slides at NHMUK; see Ryland et al. 2009, fig. 3, as W. subovoidea) with the type specimens of W. cucullata, W. subatra and W. subtorquata, indicate that W. subatra was previously misidentified as W. subtorquata by some authors (e.g. Ryland 1974; Gordon 1989; Gordon & Mawatari 1992; Mackie et al. 2006, 2012; Geller et al. 2008; Ryland et al. 2009; Láruson et al. 2012; Cockrell & Sorte 2013; Needles & Wendt 2013; Sorte & White 2013; Davis & Marshall 2014). Since Ryland et al. (2009) found the COI haplotype in colonies from Guernsey and Brittany to be identical to the commonest haplotype identified in other areas, and the morphology of the genetically identified specimens to be the same (as W. subtorquata; Mackie et al. 2006), we believe that W. subatra is the commonest putatively invasive species of Watersipora in Britain, Australia, New Zealand and California, whereas W. subtorquata is the predominant species in subtropical and tropical waters of the Atlantic and Mediterranean. Colonies from California (Figs 48–53) often have a well-demarcated, U-shaped sinus and a smooth suborificial region (without pseudopores), as has been figured in specimens from Brittany (Ryland et al. 2009, fig. 3A, D, as W. subtorquata). All specimens assigned to W. subatra have an orifice with a U-shaped sinus and narrow, bar-shaped condyles, opercula with a broad, biconcave band proximally, frontal shields with pseudopores 18–30 µm in diameter, and two latero-oral intrazooidal septula.
Soule and Soule (1975) indicated that Harmer (1957) included at least two species under Dakaria subovoidea, which may be a mixture of W. subtorquata and W. aterrima. According to the list of specimens published by Harmer (1957), however, his description and remarks included at least four species: W. subtorquata, W. cucullata, W. atrofusca and W. subatra (specimens figured from Siboga Stns 181 and 184, see Harmer 1957, pl. 49, figs 11–12, 14). Watersipora subatra is distinguished from W. subtorquata by the shapes of the orifice and condyles, and the presence of latero-oral intrazooidal septula (Figs 47, 52, 53). Latero-oral intrazooidal septula are also found in W. cucullata (Figs 8, 29, 34), W. aterrima (Fig. 37) and W. mawatarii n. sp. (Fig. 58; see below), but these species have different shapes of orifice and condyles.
Despite the wide distribution of W. subatra in Pacific waters (see Ryland et al. 2009; Mackie et al. 2012; as W. subtorquata), its occurrence in some localities in the northwest Pacific, as well as the occurrence of W. subtorquata, are unconfirmed and require morphological and molecular investigation.
Distribution. NE Atlantic (Ireland and British Isles), Indo-West Pacific (Indonesia) and Pacific (New Zealand, Australia and California).
Notes
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Linked records
Additional details
Identifiers
Biodiversity
- Collection code
- MZS , NHMUK
- Event date
- 2004-10-06
- Family
- Watersiporidae
- Genus
- Watersipora
- Kingdom
- Animalia
- Material sample ID
- MZS 002 , NHMUK 1922.10 , NHMUK 1929.12 , NHMUK 2005.5 , NHMUK 2007.12 , NHMUK 2010.12 , NHMUK 2010.6 , NHMUK 2012.6
- Order
- Cheilostomatida
- Phylum
- Bryozoa
- Scientific name authorship
- Vieira & Jones & Taylor
- Species
- subatra
- Taxonomic status
- stat. nov.
- Taxon rank
- species
- Type status
- holotype
- Verbatim event date
- 2004-10-06
- Taxonomic concept label
- Watersipora subatra (Ortmann, 1890) sec. Vieira, Jones & Taylor, 2014
References
- Ortmann, A. (1890) Die Japanische Bryozoenfauna. Bericht uber die von Herrn Dr. L. Doderlein im Jahre 1880 - 81 gemachten Sammlungen. Archiv fur Naturgeschichte, 54, 1 - 74.
- Mawatari, S. (1952) On Watersipora cucullata (Busk). I. Systematic study. Miscellaneous Reports of the Research Institute of Natural Resources (Tokyo), 25, 14 - 17.
- Harmer, S. F. (1957) The Polyzoa of the Siboga Expedition, Part 4. Cheilostomata Ascophora II. Siboga-Expeditie, 28 d, xv, 641 - 1147, pls. 42 - 74.
- Ryland, J. S. (1974) Bryozoa in the Great Barrier Reef province. In: Cameron, A. M. et al. (Eds.), Proceedings of the Second International Reef Symposium. Vol. 2. The Great Barrier Reef Committee, Brisbane, pp. 341 - 348.
- Soule, D. F. & Soule, J. D. (1975) Species groups in Watersiporidae. Bryozoa 1974. Documents des Laboratoires de Geologie de la Faculte des Science de Lyon, h. s. 3, 2, 299 - 309.
- Winston, J. E. & Heimberg, B. F. (1986) Bryozoans from Bali, Lombok, and Komodo. American Museum Novitates, 2847, 1 - 49.
- Gordon, D. P. (1989) The marine fauna of New Zealand: Bryozoa: Gymnolaemata (Cheilostomida Ascophorina) from the western South Island continental shelf and slope. New Zealand Oceanographic Institute Memoir, 97, 1 - 158.
- Gordon, D. P. & Mawatari, S. H. (1992) Atlas of marine-fouling Bryozoa of New Zealand ports and harbours. Miscellaneous Publications of the New Zealand Oceanographic Institute, 107, 1 - 52.
- Ryland, J. S., de Blauwe, H., Lord, R. & Mackie, J. A. A. (2009) Recent discoveries of alien Watersipora (Bryozoa) in Western Europe, with redescriptions of species. Zootaxa, 2093, 43 - 59.
- Kuhlenkamp, R. & Kind, B. (2013) Arrival of the invasive Watersipora subtorquata (Bryozoa) at Helgoland (Germany, North Sea) on floating macroalgae (Himanthalia). Marine Biodiversity Records, 6, e 73.
- Waters, A. W. (1909) Reports on the Marine Biology of the Sudanese Red Sea, from collections made by Cyril Crossland, M. A., B. Sc., F. Z. S.; together with collections made in the Red Sea by Dr. Hartmeyer. XII. The Bryozoa, Part 1, Cheilostomata. Linnean Society of London Journal of Zoology, 31, 123 - 181. http: // dx. doi. org / 10.1111 / j. 1096 - 3642.1909. tb 00458. x
- Hastings, A. B. (1930) Cheilostomatous Polyzoa from the vicinity of the Panama Canal collected by Dr. A. Crossland on the cruise of the S. Y. ' St. George'. Proceedings of the Zoological Society of London, 99, 697 - 740. [1929 on cover] http: // dx. doi. org / 10.1111 / j. 1096 - 3642.1929. tb 01453. x
- Mackie, J. A., Keough, M. J. & Christidis, L. (2006) Invasion patterns inferred from cytochrome oxidase I sequences in three bryozoans, Bugula neritina, Watersipora subtorquata, and Watersipora arcuata. Marine Biology, 149, 285 - 295. http: // dx. doi. org / 10.1007 / s 00227 - 005 - 0196 - x
- Geller, J., Mackie, J. A., Schroeder, G. & Gerhinger, D. (2008) Distribution of highly invasive bryozoans belonging to a cryptic species complex in the genus Watersipora determined by DNA sequences. Moss Landing Marine Laboratories, Moss Landing, 40 pp.
- Laruson, A. J., Craig, S. F., Messer, K. J. & Mackie, J. A. (2012) Rapid and reliable inference of mitochondrial phylogroups among Watersipora species, and invasive group of ship-fouling species (Bryozoa, Cheilostomata). Conservation Genetics Resources, 4, 617 - 619. http: // dx. doi. org / 10.1007 / s 12686 - 012 - 9606 - 9
- Cockrell, M. L. & Sorte, C. J. B. (2013) Predicting climate-induced changes in population dynamics of invasive species in a marine epibenthic community. Journal of Experimental Marine Biology and Ecology, 440, 42 - 48. http: // dx. doi. org / 10.1016 / j. jembe. 2012.11.008
- Needles, L. A. & Wendt, D. E. (2013) Big changes to a small bay: introduced species and long-term compositional shifts to the fouling community of Morro Bay (CA). Biological Invasions, 15, 1231 - 1251. http: // dx. doi. org / 10.1007 / s 10530 - 012 - 0362 - 2
- Sorte, C. J. B. & White, J. W. (2013) Competitive and demographic leverage points of community shits under climate warming. Proceedings of the Royal Society B, 280, 20130572. http: // dx. doi. org / 10.1098 / rspb. 2013.0572
- Davis, K. & Marshall, D. J. (2014) Offspring size in a resident species affects community assembly. Journal of Animal Ecology, 83, 322 - 331. http: // dx. doi. org / 10.1111 / 1365 - 2656.12136
- Mackie, J. A., Darling, J. A. & Geller, J. B. (2012) Ecology of cryptic invasions: latitudinal segregation among Watersipora (Bryozoa) species. Scientific Reports, 2 (871), 1 - 10. http: // dx. doi. org / 10.1038 / srep 00871