Halopteris catharina (Johnston, 1833)

Gravili, Cinzia, Vito, Doris De, Camillo, Cristina Gioia Di, Martell, Luis, Piraino, Stefano & Boero, Ferdinando, 2015, The non-Siphonophoran Hydrozoa (Cnidaria) of Salento, Italy with notes on their life-cycles: an illustrated guide, Zootaxa 3908 (1), pp. 1-187 : 101-102

publication ID

https://doi.org/10.11646/zootaxa.3908.1.1

publication LSID

lsid:zoobank.org:pub:D6AD2B49-170B-4D9C-84AA-DBE0FEEAD8BE

DOI

https://doi.org/10.5281/zenodo.6107109

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https://treatment.plazi.org/id/03F887DE-FF92-FFDC-9CD6-0DD9D307FB3E

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Plazi (2016-04-17 23:40:15, last updated 2024-11-25 23:10:55)

scientific name

Halopteris catharina (Johnston, 1833)
status

 

Halopteris catharina (Johnston, 1833) View in CoL

Fig. 71 View FIGURE 71 A–D

See Schuchert (1997) for a complete synonymy.

Material examined. HCUS-S 0 78 (Hydrozoa Collection, University of Salento—fauna of the Salento Peninsula).

Description (based on our own observations; Schuchert 1997):

Hydroid. Hydrorhiza as branched stolons; colonies pinnate, up to 40 mm high; hydrocauli monosiphonic, unbranched, basal part composed of several segments bearing 2 longitudinal rows of nematothecae, nodes transverse, remaining stem axis heteromerously segmented by alternating oblique and transverse nodes; hydrocladia opposite, borne laterally below hydrothecae, on long stem apophyses, hydrothecate segments with one hydrotheca and 5 nematothecae, one median inferior and 2 pairs of lateral ones, non-hydrothecate segments with 1–4 nematothecae, hydrocladia with a first athecate segment, remaining segments as in the main axis, but nonhydrothecate ones with 1–2 nematothecae; hydrothecae cup-shaped, walls straight almost parallel, in the middle of the internode, 1/2 adnate, rim smooth, aperture at 45º from the axis; nematothecae all two-chambered and movable, upper chamber with a deep embayment, outer pair of lateral nematothecae reaching the rim or slightly beyond it, on long apophyses, inner pair at base of those apophyses. Gonothecae of both sexes on the same plume, developing on main segments below hydrotheca of stem and hydrocladia, female ones cylindrical, somewhat flattened, narrowed at base, with 2 nematothecae, truncated distally, with annular thickening and lid, basal pedicel with 2 segments, male ones smaller and elongated. Colour: all tissues colourless.

Cnidome. Microbasic mastigophores.

Habitat type. Rocky, depth range down to 412 m (Gili et al. 1989; Ramil & Vervoort 1992).

Substrate. Terebellid tubes, Ascidiacea, algae, hydroids.

Seasonality. January–April, June–August, December (Gili 1986) in the western Mediterranean; October (De Vito 2006; this study) in Salento waters.

Reproductive period. March, June (Gili 1986) in the western Mediterranean Sea.

Distribution. Temperate and southern-boreal regions of the eastern and western sides of the Atlantic, Mediterranean (Ramil & Vervoort 1992; Medel & López-González 1996; Schuchert 1997; Bouillon et al. 2004; Gravili et al. 2008a; Bianchi et al. 2011).

Records in Salento. Rare at Otranto (De Vito 2006; Gravili 2006; Gravili et al. 2008a; this study).

Remarks. Halopteris catharina is easily recognisable for its rather distinct plumose habit with opposite hydrocladia, but it can also occur in forms differing from the typical plumose stems. Therefore, population genetic methods are needed for correct identification (for more details see Thorpe et al. 1992).

References. Russell (1957), Picard (1958a), Gili (1986), Ramil & Vervoort (1992), Medel & López-González (1996), Schuchert (1997), Ansín Agís et al. (2001), Bouillon et al. (2004), Morri & Bianchi (1999), Morri et al. (1999), De Vito (2006), Gravili (2006), Gravili et al. (2008a), Bianchi et al. (2011).

Ansin Agis, J., Ramil F. & Vervoort, W. (2001) Atlantic Leptolida (Hydrozoa, Cnidaria) of the families Aglaopheniidae, Halopteriidae, Kirchenpaueriidae and Plumulariidae collected during the CANCAP and Mauritania-II expeditions of the National Museum of Natural History, Leiden, the Netherlands. Zoologische Verhandelingen Leiden, 333, 1 - 268.

Gravili, C., Boero, F. & Licandro, P. (2008 a) Hydrozoa. Biologia Marina Mediterranea, 15 (Supplement), 71 - 91.

Bianchi, C. N., Dando, P. R. & Morri, C. (2011) Increased diversity of sessile epibenthos at subtidal hydrothermal vents: seven hypotheses based on observations at Milos Island, Aegean Sea. Advances in Oceanography and Limnology, 2 (1), 1 - 31. http: // dx. doi. org / 10.1080 / 19475721.2011.565804

Medel, M. D. & Lopez-Gonzalez, P. J. (1996) Updated catalogue of the Hydrozoans from the Iberian Peninsula and Balearic Islands with remarks on zoogeography and affinities. Scientia Marina, 60 (1), 183 - 209.

Picard, J. (1958 a) Origines et affinites de la faune d'hydropolypes (Gymnoblastes et Calyptoblastes) et d'hydromeduses (Anthomeduses et Leptomeduses) de la Mediterranee. Rapports et proces verbaux des Reunions de la Commission Internationale pour l'Exploration Scientifique de la Mer Mediterranee Monaco, 14, 187 - 199.

Russell, F. S. (1957) Coelenterata. In: Plymouth marine fauna. Marine Biological Association of the United Kingdom, Plymouth, pp. 37 - 69.

Schuchert, P. (1997) Review of the family Halopterididae (Hydrozoa, Cnidaria). Zoologische Verhandelingen Leiden, 309, 1 - 162.

Thorpe, J. P., Ryland, J. S., Cornelius, P. F. S. & Beardmore, J. A. (1992) Genetic divergence between branched and unbranched forms of the thecate hydroid Aglaophenia pluma. Journal of the Marine Biological Association of the United Kingdom, 72 (4), 887 - 894. http: // dx. doi. org / 10.1017 / s 0025315400060124

Gallery Image

FIGURE 71. Halopteris catharina: A, normal plumose colony; B, part of caulus with opposite branched hydrocladia; C, part of hydrocladium with main segment and intersegment; D, gonothecae: left female, right male (redrawn and modified after Schuchert 1997 by C. G. Di Camillo). Scale bars: A, 5.0 mm; B, 0.5 mm; C, D, 0.2 mm.