Leucascus clavatus Dendy, 1892
publication ID |
https://doi.org/ 10.11646/zootaxa.3619.3.3 |
publication LSID |
lsid:zoobank.org:pub:92C07D63-F2F5-4898-A7FE-4937F4D5A043 |
DOI |
https://doi.org/10.5281/zenodo.6153180 |
persistent identifier |
https://treatment.plazi.org/id/038E706D-EC11-744D-FF17-2ED7C0BEFEE3 |
treatment provided by |
Plazi |
scientific name |
Leucascus clavatus Dendy, 1892 |
status |
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Leucascus clavatus Dendy, 1892 View in CoL
Diagnosis: Presence of club-shaped diactines perpendicular to the sponge surface. Apical actine of tetractines with well developed spines, and a ring at the base.
Synonymies: Leucascus clavatus Dendy 1892: 78 ; Dendy & Row 1913: 731; Brøndsted 1926 (?): 300; Row & Hôzawa 1931: 743; Burton 1963: 241.
Type material: BMNH 1893.6.9.2 and NMV F42333 View Materials (Holotypes—two fragments of the same specimen; near Port Phillip Heads, Australia; Wilson collection).
Type locality: Port Phillip Heads, Australia.
Additional analysed material: BMNH 1925.11.1.1727 (Port Phillip Heads, Australia; Dendy collection, R.N. 240), BMNH 1924.2.6.53 (Wilson collection), BMNH 1925.11.1.1726 (near Port Phillip Heads, Australia; R.N. 196), BMNH 1925.11.1.1728 (near Port Phillip Heads, Australia; R.N. 241), WAM Z40143 (Jack Reef, Dongara, Western Australia, 2918.85’S 11454.7’E; coll. J. Fromont, CS Whisson & GI Moore; 15.03.2006; depth: 6.5 m), WAM Z40519 (Jurien Bay, Julia Rocks, Western Australia, 30 09.34’S 114 59.83’E; coll. G. Clapin, R. Babcock & A. Sampey; 03/V/2005; depth: 5.6- 5 m), WAM Z40521 (Jurien Bay, Julia Rocks, Western Australia, 30 09.34’S 114 59.83’E; coll. G. Clapin, R. Babcock & A. Sampey; 03/V/2005; depth: 5.6- 5 m), and NMV F42334 View Materials (a fragment of BMNH 1925.11.1.1728).
Description: The colour of this species alive is unknown but after fixation it is beige ( Figure 3 View FIGURE 3 A). The cormus is massive and its consistency is firm but compressible. The cormus is formed by anastomosed tubes covered by a thin and smooth membrane. The WAM specimens have a rounded shape ( Figure 3 View FIGURE 3 A) and their surfaces are a little ridged. The osculum is single, large (ca. 7 mm in diameter in the specimens from WAM) and without ornamentation. The atrial cavity is also surrounded by a thin membrane, which was not observed in the specimen NMV F42333 View Materials , probably due to its preservation. Reproductive structures were found in the specimen BMNH 1924.2.6.53.
The skeleton is composed of diactines, triactines, and few tetractines. Diactines are present mainly near the osculum and their abundance varies from rich to rare among the analysed specimens. They lay mainly perpendicular to the surface ( Figure 3 View FIGURE 3 B), but they can also be found below the cortical membrane ( Figure 3 View FIGURE 3 C). These latter are rare and shorter than the protruding diactines. The skeleton of the cortical membrane is also composed of triactines and some rare tetractines ( Figure 3 View FIGURE 3 D). These spicules are also present in the tubes ( Figure 3 View FIGURE 3 E), where the tetractines project their apical actines into the lumen ( Figure 3 View FIGURE 3 F). The atrial skeleton is composed exclusively of triactines ( Figure 4 View FIGURE 4 A).
Spicules/ Specimens Actine Length (µm) Width (µm) N
Min Mean SD Max Min Mean SD Max Triactine
BMNH 1893.6.9.2 (H) 97.2 124.7 13.5 162.8 10.9 14.6 1.8 18.2 30 NMV F42333 View Materials (= BMNH 1925.11.1.1726) 85.0 117.4 15.3 138.5 9.7 13.3 1.5 15.8 30 NMV F42334 View Materials (= BMNH 1925.11.1.1728) 72.9 106.1 15.6 145.8 10.9 14.5 2.3 19.4 30 All specimens 72.9 116.1 7.6 162.8 9.7 14.5 1.0 19.4 – Tetractine Basal
BMNH 1893.6.9.2 (H) 97.2 120.3 11.5 140.9 9.7 13.3 1.4 15.8 30 NMV F42333 View Materials (= BMNH 1925.11.1.1726) 72.9 110.2 12.9 133.6 9.7 11.7 1.5 14.6 30 NMV F42334 View Materials (= BMNH 1925.11.1.1728) 85.0 107.6 9.6 131.2 9.7 12.5 1.7 14.6 30 All specimens 72.9 112.7 5.5 140.9 9.7 12.5 0.6 15.8 –
Apical
BMNH 1893.6.9.2 (H) 24.3 43.2 7.1 60.7 2.4 4.6 0.9 7.3 30 NMV F42333 View Materials (= BMNH 1925.11.1.1726) 36.4 48.1 5.9 60.7 3.6 4.7 0.8 7.3 30 NMV F42334 View Materials (= BMNH 1925.11.1.1728) 36.4 43.3 7.0 60.7 3.6 4.4 0.6 4.9 16 All specimens 24.3 44.9 2.3 60.7 2.4 4.6 0.1 7.3 – Diactine
BMNH 1893.6.9.2 (H) – – – – – – – – 0 NMV F42333 View Materials (= BMNH 1925.11.1.1726) 500.0 663.6 156.0 850.0 70.0 101.8 14.0 120.0 11 NMV F42334 View Materials (= BMNH 1925.11.1.1728) 350.0 614.0 144.0 850.0 50.0 96.7 27.4 140.0 15 All specimens 350.0 638.8 24.8 850.0 50.0 99.2 2.6 140.0 – Spicules ( Table 2):
(i) Diactines ( Figure 4 View FIGURE 4 B): Variable in size. They are club-shaped, with the sharp tip inside the sponge and the rounded one projected outside;
(ii) Triactines ( Figure 4 View FIGURE 4 C): Regular, with conical actines and sharp tips. Some rare triactines have an elevated centre;
(iii) Tetractines ( Figure 4 View FIGURE 4 C): Similar to the triactines, but with an apical actine, which is shorter and thinner than the basal ones. It presents well developed spines, and has a characteristic ring at their base ( Figure 4 View FIGURE 4 D).
Remarks: Spines on the apical actines have never been observed in Leucascus clavatus . Neither has the ring present at the base of the apical actine. The spines of the apical actine showed no special pattern. The ring and the club-shaped diactines are diagnostic characters of L. clavatus . In fact, up to date L. clavatus is the only species of the genus with diactines (the species Leucascus albus sp. nov. has microdiactines). It is possible, however, that there are other Leucascus species with diactines in their skeletons. Brøndsted (1926) identified specimens from New Zealand as L. clavatus based on the presence of diactines where both tips were sharp. These specimens are clearly not L. clavatus , as the diactines were not club-shaped. Brøndsted’s specimens most likely represent a new species of Leucascus . Unfortunately, in the present work these specimens from New Zealand could not be analysed.
Distribution: Indian and Pacific Oceans: Port Phillip Heads (Dendy 1892), Geraldton District (Row & Hôzawa 1931), and Jurien Bay and Dongara—Australia; Halfmoon Bay, Stewart Island—New Zealand (Brøndsted 1926). Spalding et al. (2007) correponding ecoregions are: Bassian, Houtman, and Snares Islands.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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