Published March 13, 2020 | Version v1
Taxonomic treatment Open

Cladocarpus asymmetricus Galea 2020, sp. nov.

  • 1. Hydrozoan Research Laboratory, 405 Chemin Les Gatiers, 83170 Tourves, France.

Description

Cladocarpus asymmetricus sp. nov.

urn:lsid:zoobank.org:act: 765A957F-FEF6-47A6-B09A-314F31F0440E

Figs 1 D–E, 4; Table 1

Diagnosis

Cladocarpus with lightly fascicled, unbranched stems divided into fairly long internodes, each with 2–3 frontal nematothecae, a mamelon and an axillar nematotheca. Cladia close to one another. Cormidia with up to 7 intranodal, adaxial septa. Hydrothecae elongated, asymmetrical in frontal view, with two lateral transverse ridges projecting into the lumen, rim with 9 rounded cusps. Phylactocarps given off from first cormidium, gonothecae concrescent with the rachis basally, crescent-shaped, with three types of nematothecae on both body and apex.

Etymology

From the Latin ‘ ăsymmĕtĕr, -tra, -trum ’, meaning ‘asymmetrical’, with reference to the shape of the hydrotheca in frontal view.

Material examined

Holotype

PACIFIC OCEAN • 1 single plume, ca 8.5 cm high, hydrorhiza missing; off New Caledonia, stn DW4979; 19°42ʹ S, 158°37ʹ E; 315– 295 m; 9 Sep. 2017; KANADEEP leg.; MNHN-IK-2015-530.

Description

Colony erect, at least 8.5 cm high, hydrorhiza missing. Stem unbranched, fairly fascicled, accessory tubes forming a beam around the main tube; no deeply-cut, proximal, oblique nodes; elsewhere division into internodes indistinct, except for distalmost, monosiphonic part, with thinner perisarc, where transverse nodes (165–180 µm wide) delimit rather long (820–1030 µm) internodes composed of 2–3 (occasionally 4) proximal nematothecae in a row, a lateral cladial apophysis with its associated conical nematotheca (with rounded, apical aperture), and an axillar nematotheca rather lateral to the apophysis; dorsal axillar nematotheca absent; all stem nematothecae sac-shaped, adnate for ⅔ of their length, with apical, guttershaped aperture facing adaxially; each accessory tube of the stem with a row of saccate, deeply immersed nematothecae, with only their ovoid apertures slightly protruding from the perisarc. Cladial apophyses alternate along the stem, ending distally in a deeply oblique node; cladia close to one another, up to 1.9 cm long, divided into rather long internodes (1025–1090 µm) by means of slight, transverse (115– 120 µm wide) constrictions of the perisarc, each accommodating a hydrotheca and its 3 nematothecae: one mesial and a pair of laterals flanking the aperture. Hydrotheca elongated, 895–950 µm deep, slightly compressed laterally below the rim, with straight adaxial and slightly curved abaxial walls, with an intrathecal septum given off from the lower ¼ of the adaxial wall, and projecting for a short distance into the lumen; in frontal view, lower part of hydrotheca asymmetrical, due to the presence of two conspicuous, semicircular, intrathecal plates given off at two different levels from the lateral walls; free edges slightly overlapping in the middle of the lumen; in a lateral view of the hydrotheca, the attachment sites of these septa are distinctly sigmoid. Mesial nematotheca long, tubular, adnate for about ¾ its length, leaving distally a short (90–95 µm), gutter-shaped aperture; lateral nematothecae short (195–200 µm), tubular, tapering towards the distal aperture, the latter with deeply scooped margin on adaxial side. Hydrothecal aperture 300–305 µm wide, rim with 9 cusps: one median, abaxial with squared outline, and 4 pairs of laterals, the latter triangular in shape, with rounded tips, becoming gradually lower and wider towards the adaxial side of the theca; up to 7 intranodal septa, all given off from the adaxial wall of the hydrothecae and projecting for a relatively short distance into the lumen of the internode; of these, 2 cusps are given off from the adaxial thecal wall below the intrahydrothecal septum, while up to 5 others from above it. Phylactocarp given off laterally from first cormidium, borne on distinct, athecate apophysis with distal, oblique node; phylactocarp up to 6 mm long, composed of a slightly geniculate rachis divided into up to 20 short (250–305 µm) internodes by means of slightly-marked, transverse nodes; each internode with a proximal nematotheca, a basally concrescent gonotheca, and a second nematotheca lateral to its insertion (both nematothecae elongated, with scooped rims adaxially); the proximalmost internode has an extra proximal nematotheca. Gonothecae crescent-shaped in lateral view, ca 850 × 250 µm, those with curvature on one side alternating with those curved oppositely from the other side; circular in transverse section, tapering gently below and gradually above to form a pointed apex bearing a nematotheca with scooped rim; two dissimilar nematothecae, placed at nearly the same level on the adaxial side of the thecal wall, at about ⅓ of the length above from the insertion of the gonotheca on the rachis: one nematotheca is conical, with thick walls and has a small, slightly scooped aperture, while the other is barrel-shaped, with thin walls and has a broad, circular aperture with entire margin; upper third of the adaxial gonothecal wall with 1 (occasionally 2) sac-shaped nematotheca(e) with scooped rim on adaxial side.

Remarks

The relationships between several related aglaopheniid genera, viz. Cladocarpus Allman, 1874, Aglaophenopsis Fewkes, 1881, Streptocaulus Allman, 1883 and Nematophorus Broch, 1918, have been discussed and interpreted by a number of authors (e.g., Ramil & Vervoort 1992a; Ansín Agís et al. 2001; Altuna et al. 2013) on the account of morphological characters alone. To these should be added other genera, such as Carpocladus Vervoort & Watson, 2003, Cladocarpoides Bogle, 1984 and Wanglaophenia Vervoort & Watson, 2003, that make the case even more complex and, taken globally, it becomes evident that only a genetic study can be expected to clarify their relationships objectively.

The present hydroid, as well as Cladocarpus partitus sp. nov. and C. pennatus sp. nov. (see below), have gonosomes that do not conform accurately to any diagnosis of the abovementioned genera, displaying only some of their characters, as well as additional, distinctive ones. For this reason, these three new species are provisionally accommodated in the genus Cladocarpus, the oldest available name, pending a future phylogenetic study based on molecular markers.

A few congeners have hydrothecae resembling those of C. asymmetricus sp. nov., notably with respect to their elongated appearance and the presence of two lateral, oblique, intrathecal ridges. Their distinctive features are summarized in Table 1.

The new species is also highly distinctive in that its gonothecae are provided with nematothecae, a situation unknown in any of the Cladocarpus -like species described so far. Moreover, these nematothecae have three different morphologies and are present at different positions on the gonotheca.

Distribution

Known only from its type locality, off New Caledonia (present study).

Notes

Published as part of Galea, Horia R., 2020, Aglaopheniid hydroids (Cnidaria: Hydrozoa: Aglaopheniidae) from off New Caledonia collected during KANACONO and KANADEEP expeditions of the French Tropical Deep-Sea Benthos Program, pp. 1-47 in European Journal of Taxonomy 615 on pages 5-9, DOI: 10.5852/ejt.2020.615, http://zenodo.org/record/3711000

Files

Files (11.5 kB)

Name Size Download all
md5:76403700377ece7159b890a6f314e20b
11.5 kB Download

System files (44.3 kB)

Name Size Download all
md5:158d597a8a5588332353a304aae6be20
44.3 kB Download

Linked records

Additional details

Biodiversity

Collection code
MNHN
Event date
2017-09-09
Family
Aglaopheniidae
Genus
Cladocarpus
Kingdom
Animalia
Material sample ID
MNHN-IK-2015-530.
Order
Leptothecata
Phylum
Cnidaria
Scientific name authorship
Galea
Species
asymmetricus
Taxonomic status
sp. nov.
Taxon rank
species
Type status
holotype
Verbatim event date
2017-09-09
Taxonomic concept label
Cladocarpus asymmetricus Galea, 2020

References

  • Bedot M. 1921. Hydroides provenant des campagnes des Yachts Hirondelle et Princesse-Alice (1887 - 1912). Resultats des Campagnes scientifiques accomplies sur son Yacht par Albert Ier Prince souverain de Monaco 60: 1 - 74.
  • Ramil F., Vervoort W. & Ansin Agis J. 1998. Report on the Haleciidae and Plumularioidea (Cnidaria, Hydrozoa) collected by the French Seamount 1 Expedition. Zoologische Verhandelingen, Leiden 322: 1 - 42. Available from https: // www. repository. naturalis. nl / document / 149163 [accessed 6 Mar. 2020].
  • Vervoort W. & Watson J. E. 2003. The marine fauna of New Zealand: Leptothecata (Cnidaria: Hydrozoa) (thecate hydroids). NIWA Biodiversity Memoir 119: 1 - 538. Available from https: // archive. org / details / niwabiodiversitymemoir 01192003 [accessed 6 Mar. 2020].
  • Allman G. J. 1877. Report on the Hydroida collected during the exploration of the Gulf Stream by L. F. de Pourtales, Assistant United States Coast Survey. Memoirs of the Museum of Comparative Zoology at Harvard College 5 (2): 1 - 66. https: // doi. org / 10.5962 / bhl. title. 10420
  • Bogle M. A. 1975. A Review and Preliminary Revision of the Aglaopheniinae (Hydroida: Plumulariidae) of the Tropical Western Atlantic. MSc Thesis, University of Miami, Coral Gables, USA.
  • Vervoort W. 1972. Hydroids from the Theta, Vema and Yelcho cruises of the Lamont-Doherty Gological Observatory. Zoologische Verhandelingen, Leiden 120: 1 - 247. Available from https: // www. repository. naturalis. nl / document / 149147 [accessed 6 Mar. 2020].
  • Schuchert P. 2015. On some hydroids (Cnidaria, Hydrozoa) from the Okinawa Islands, Japan. Revue suisse de Zoologie 122 (2): 325 - 370. https: // doi. org / 10.5281 / zenodo. 30004
  • Fewkes J. W. 1881. Report on the Acalephae. In: Reports on the results of dredging, under the supervision of Alexander Agassiz, in the Caribbean Sea, in 1878, 1879, and along the Atlantic coast of the United States, during the summer of 1880, by the U. S. Coast Survey Steamer Blake. Bulletin of the Museum of Comparative Zoology, at Harvard College 8 (7): 127 - 140. Available from https: // www. biodiversitylibrary. org / page / 28870347 [accessed 6 Mar. 2020].
  • Allman G. J. 1883. Report on the Hydroida dredged by H. M. S. Challenger during the years 1873 - 76. Part I. - Plumularidae. Report on the Scientific Results of the Voyage of H. M. S. Challenger during the Years 1873 - 76, Zoology 7 (20): 1 - 55. https: // doi. org / 10.5962 / bhl. title. 11299
  • Broch H. 1918. Hydroida (Part II). Danish Ingolf-Expedition 5 (7): 1 - 206.
  • Ramil F. & Vervoort W. 1992 a. Some consideration concerning the genus Cladocarpus (Cnidaria: Hydrozoa). Scientia Marina 56 (2 - 3): 171 - 176. Available from http: // scimar. icm. csic. es / scimar / pdf / 56 / sm 56 n 2171. pdf [accessed 6 Mar. 2020].
  • 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, Leiden 333: 1 - 268. Available from https: // repository. naturalis. nl / document / 46286 [accessed 6 Mar. 2020].
  • Altuna A., Murillo F. J. & Calder D. R. 2013. Aglaopheniid hydroids (Cnidaria: Hydrozoa: Aglaopheniidae) from bathyal waters of the Flemish Cap, Flemish Pass, and Grand Banks of Newfoundland (NW Atlantic). Zootaxa 3757 (5): 501 - 537. https: // doi. org / 10.11646 / zootaxa. 3737.5.1
  • Bogle M. A. 1984. Cladocarpoides yucatanicus, a new genus and species of Aglaopheniinae (Coelenterata: Hydroida: Plumulariidae) from Arrowsmith Bank, Yucatan Channel. Bulletin of Marine Science 34 (1): 135 - 140.