Published May 12, 2020 | Version v1
Taxonomic treatment Open

Lycopodina helios Ekins & Erpenbeck & Hooper 2020, sp. nov.

Description

Lycopodina helios sp. nov.

Figure 29, Table 14

urn:lsid:zoobank.org:act: 91243F13-A9BC-4958-8DB8-EEAB28792C85

Material examined: Holotype: QM G337468, off Cape Barren Island, Flinders Central Marine Reserve, Tasman Sea, NE Tasmania, Australia, Station 16, 40° 27’ 46.8”– 40° 27’ 40.3” S, 149° 24’ 54.0”– 149° 21’ 50.4” E, 4129– 4321 m depth, Brenke Epibenthic Sledge, Coll. Merrick Ekins on RV Investigator, Cruise IN2017_ V03, Sample 16-140, 21/v/2017.

Etymology: Gr. Helios, the sun refering to the sponges bright radiant morphology

Distribution: This species is currently restricted to Tasmania, Australia, at abyssal depth.

Description:

Growth form: A delicate erect pedunculate sponge with a subspherical club-shaped body and a long slender stem (Figure 29 G–H). Total length of the sponge is 16.6 mm, the majority of this being the stem of 11.3 mm. The width of the sponge body is 4 mm and diameter of the stem is less than 1 mm. The basal attachment was not collected.

Colour: Yellow on-deck and in ethanol.

Ectosomal skeleton: The remains of a very thin ectosomal membrane bearing the anisochelae can be seen covering the body of the sponge. This membrane is supported by the projecting subtylostyles (Figure 29 I).

Endosomal skeleton: The axis of the stem is cored by dense longitudinally arranged subtylostyles (Figure 29 J). The body has subtylostyles radiating in every direction, with the longer of these projecting through the membranous ectosome. Adjacent radiating subtylostyles often cluster together to form filaments covered in anisochelae (Figure 29 I).

Megascleres: Subtylostyles with long tapering points and narrowed or slightly subtylote bases, with the largest diameter of styles approximately at their centre. However, there is no clear size delineation of the megascleres, (508-(849)- 1770 x 8.2-(13.1)-18.9 μm, n=63) (Figure 29 B–E).

Microscleres: Palmate anisochelae with three smooth upper alae, the central one nearly fully detached, and the two lateral ones fused to the fimbria. The lower frontal alae has three terminal spines and the lower lateral alae each have two spines. Anisochelae length (15.5-(21.4)-25.5 μm x 4.5-(7.1)-9.4 μm (large alae width), 3.3-(5.2)-6.7 μm (small alae width) (Figure 29 A). Sigmancistras were also found (12.2-(16.0)-18.5 x 1.0-(1.4)-2.3 μm, n=46) (Figure 29 F).

Molecular data: The 28S sequence of QM G337468 is provided in the Sponge Barcoding Database under accession number SBD#2306 and the molecular difference to other congenerics displayed in Figure 3.

Remarks: This new species of Lycopodina has a more spherical shaped body of a much smaller size than its most similar species, L. callithrix (Hentschel, 1914). In addition this species differs in the shape of the anisochelae, which are much larger than those of L. callithrix reported by Hentschel (1912) and Koltun (1964). This species also lacks the very large styles/ subtylostyles (2000–4000 µm) that are present in L. callithrix. This species is also unique in having the ectosomal membrane containing the anisochelae supported by the subtylostyles (Figure 29 I).

This new species shares a similar morphology size and shape as L. callithrix reported by Dressler-Allame et al. (2017), as well as anisochelae (9–22 x 4–9 µm) and style/subtylostyle (180– 1600 x 7–18 µm) measurements. Possibly some or all of the specimens of L. callithrix reported by Dressler-Allame et al. (2017) could belong to this new species. Molecular techniques may in the future confirm if they are conspecific.

The description of L. communis (Lopes & Hajdu, 2014) from the Campos Basin off Brazil is also very similar to that of L. callithrix, both sharing a similar gross morphology, the size and dentition of the anisochelae, and the size range of mycalostyles falling within the size range of the specimens described by Dressler-Allame et al. (2017). Molecular techniques may in the future confirm whether or not they might be conspecific, despite their very disjunct biogeographic ranges.

Notes

Published as part of Ekins, Merrick, Erpenbeck, Dirk & Hooper, John N. A., 2020, Carnivorous sponges from the Australian Bathyal and Abyssal zones collected during the RV Investigator 2017 Expedition, pp. 1-159 in Zootaxa 4774 (1) on pages 144-146, DOI: 10.11646/zootaxa.4774.1.1, http://zenodo.org/record/3825140

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Linked records

Additional details

Biodiversity

Collection code
QM, NE, RV
Event date
2017-05-21
Family
Cladorhizidae
Genus
Lycopodina
Kingdom
Animalia
Material sample ID
G337468, V03
Order
Poecilosclerida
Phylum
Porifera
Scientific name authorship
Ekins & Erpenbeck & Hooper
Species
helios
Taxonomic status
sp. nov.
Taxon rank
species
Type status
holotype
Verbatim event date
2017-05-21
Taxonomic concept label
Lycopodina helios Ekins, Erpenbeck & Hooper, 2020

References

  • Hentschel, E. (1914) Monaxone Kieselschwamme und Hornschwamme der Deutschen Sudpolar-Expedition 1901 - 1903. Deutsche Sudpolar-Expedition, 15 (1), 35 - 141, pls. IV-VIII.
  • Koltun, V. M. (1964) Sponges of the Antarctic. 1 Tetraxonida and Cornacuspongida. In: Pavlovskii, E. P., Andriyashev, A. P. & Ushakov, P. V. (Eds.), Biological Reports of the Soviet Antarctic Expedition (1955 - 1958), 1964, pp. 6 - 133 + 443 - 448.
  • Dressler-Allame, M., Gocke, C., Kersken, D., Plotkin, A. & Janussen, D. (2017) Carnivorous sponges (Cladorhizidae) of the deep Weddell Sea, with description of two new species. Deep-Sea Research II, 4121, 190 - 206. https: // doi. org / 10.1016 / j. dsr 2.2016.08.006
  • Lopes, D. A. & Hajdu, E. (2014) Carnivorous sponges from deep-sea coral mounds in the Campos Basin (SW Atlantic), with the description of six new species (Cladorhizidae, Poecilosclerida, Demospongiae). Marine Biology Research, 10 (4), 329 - 356. https: // doi. org / 10.1080 / 17451000.2013.797587