Published April 30, 2005 | Version v1
Taxonomic treatment Open

Ophiocomina nigra

Creators

Description

OPHIOCOMINA NIGRA (ABILDGAARD, IN O.F. MÜLLER, 1789)

(FIG. 17A–M)

All stages studied here had a dark brown, almost black colour, which makes them unique among the species found at the Swedish west coast and thus easily identifiable. The smallest specimens available measure 0.7 mm dd with seven arm segments. The dorsal disc is formed by the round CPP and five RPPs, triangular SIRs, IR1 and the round k-plate above the distal ends of the RSs (Fig. 17A). All plates are almost imperforate, except for small holes on their margins particularly under a disc spine. The disc spines are conical and rugose. Each LAP bears three erect serrated spines. The DAP is triangular, slightly wider than long, with strongly convex distal edge, and adjacent plates separated by the LAPs. Another individual of 0.7 mm dd has fewer SIRs, and slightly larger IRs (Fig. 17B). The MP are rugose and spiniform, one on the DP and another on the oral plate, both half as long as the spine-like tooth (Fig. 17C). On some jaws a third lower papilla is present on the distal end of the oral plate. There is a strong, rugose ASS in the middle of the concave edge of the long distally flaring AS. The OS is teardrop-shaped, wrapped around the raised edge of the oral frame. Several round evenly perforated scales form the ventral disc. On the proximal arm segments, the TPo bears a single small rugose scale, which does not cover the pore. The VAPs are longer than wide, with convex distal edge, proximal angle and deeply concave lateral edges. The first VAP is similar to the others except for a convex proximal edge. Adjacent plates are separated by the LAPs.

At 0.9 mm dd, the number of disc scales has increased considerably. Most disc spines are shorter granules, but some are still conical spines, all of which are rugose (Fig. 17D). The oral plates bear two MP, the distal one lower and wider than the proximal papilla (Fig. 17E).

At 1.4 mm dd, the numerous dorsal disc scales are partially obscured by rugose granules (Fig. 17F). There are now four strongly serrated arm spines, the dorsalmost being the longest, longer than an arm segment (Fig. 17G). Of the RSs only the distal edge is visible beneath the disc scales. The MP on the DP have moved closer towards each other, forming an apical pair below the first tooth (Fig. 17H). The TS is flat, oval and covers the pore. Bursal slits are visible above the arm. Numerous round overlapping scales form the ventral disc.

With increasing size, the number of disc granules (Fig. 17K) increases until the dorsal disc is completely covered. At 1.6 mm dd, the ASS has moved to the oral plate and a small papilla has formed on the proximal side of the ASS (Fig. 17I). The ASs are long, pairs forming a wide angle. The OS is twice as wide as long with slightly protruding distal edge. The first VAP is smaller than the others, hexagonal with straight edges. On the first ‘true’ arm segment a second smaller TS has formed. The arm spines are pointed with strongly serrated lateral edges (Fig. 17J).

At 2.4 mm dd, the ASS and its adjacent papilla have been incorporated into the row of lateral MP, thus counting a total of five, with the apical pair close together, ventral to the first tooth (Fig. 17L). The ventral disc is covered with round, imbricating scales with small round perforations, bearing no granules.

At 3 mm dd, additional apical MP can be seen below the apical pair (Fig. 17M), an indication of the apical cluster of the adult, making this the smallest size at which keys for adults can be used. Each TPo bears a pair of one smaller and one larger, flat, oval scale. The VAP are contiguous, slightly overlapping on the proximal segments, with straight distal edge. The AS is long and narrow, almost horizontal to the jaw, bordering the proximal angle of the OS, without separating it from the first LAP. The OS is twice as wide as long, with a low protrusion in the middle of the distal edge.

Remarks: This shallow-water species can easily be identified in all growth stages by its dark brown to black colour, already present in small postlarvae, and its granulated dorsal disc. The genus Ophiocomina has been argued to belong within the Ophiacanthidae instead of the Ophiocomidae (Wilkie, 1980), but this has been refuted by Baker & Devaney (1981). The serrated spines and rugose disc granules and mouth papillae certainly bear closer similarities to Ophiacanthidae than to Ophiocomidae. However, small stages of Ophiocomidae were not available for comparison, leaving this question undecided. In addition, the Ophiacanthidae has been suggested to be paraphyletic (Smith et al., 1995), which makes the systematic status of O. nigra even more difficult to understand. Until this question is resolved it is retained in the Ophiocomidae.

Notes

Published as part of Stöhr, Sabine, 2005, Who's who among baby brittle stars (Echinodermata: Ophiuroidea): postmetamorphic development of some North Atlantic forms, pp. 543-576 in Zoological Journal of the Linnean Society 143 (4) on pages 569-572, DOI: 10.1111/j.1096-3642.2005.00155.x, http://zenodo.org/record/5432948

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Linked records

Additional details

Biodiversity

Family
Ophiotomidae
Genus
Ophiocomina
Kingdom
Animalia
Order
Ophiacanthida
Phylum
Echinodermata
Scientific name authorship
Abildgaard in O. F. Muller
Species
nigra
Taxon rank
species
Taxonomic concept label
Ophiocomina nigra (Muller, 1789) sec. Stöhr, 2005

References

  • Wilkie IC. 1980. The systematic position of Ophiocomina Koehler and a reconsideration of certain interfamilial relationships within the Ophiuroidea. In: Jangoux M, ed. Echinoderms: present and past. Rotterdam: Balkema, 151 - 157.
  • Baker AN, Devaney DM. 1981. New records of Ophiuroidea (Echinodermata) from Southern Australia, including new species of Ophiacantha and Ophionereis. Transactions of the Royal Society of Southern Australia 105: 155 - 178.
  • Smith AB, Paterson GLJ, Lafay B. 1995. Ophiuroid phylogeny and higher taxonomy: morphological, molecular and palaeontological perspectives. Zoological Journal of the Linnean Society 114: 213 - 243.