Bathelia candida Moseley, 1881
publication ID |
https://doi.org/ 10.11646/zootaxa.3691.1.2 |
publication LSID |
lsid:zoobank.org:pub:D25D3DD9-8C09-4F9B-91AB-48853F444756 |
DOI |
https://doi.org/10.5281/zenodo.6151591 |
persistent identifier |
https://treatment.plazi.org/id/03FD87D6-D236-1413-FF6A-939035AD504A |
treatment provided by |
Plazi |
scientific name |
Bathelia candida Moseley, 1881 |
status |
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Bathelia candida Moseley, 1881 View in CoL
Figs. 1 View FIGURE 1. A B, 2A–C, 5
Bathelia candida Moseley, 1881: 177 –178, pl. 8, figs. 1–6.—Cairns, 1982: 13, pl. 3, figs. 1–3, Map 1 (re-description and illustrations).—Kitahara & Cairns, 2005: fig. 2E.—Kitahara, 2007: 500, 501 (listed).—Kitahara et al., 2009: 228 (listed).
Remarks. The species was well described by Cairns (1982). The uncommon asexual reproduction mode of distomadeal intratentacular budding, alluded to by Cairns (1982), is illustrated herein ( Fig. 2A View FIGURE 2. A – C ). Septa of the four cycles are virtually indistinguishable in size, all being uniformly narrow with finely dentate axial edges, although the S1–2 are sometimes slightly exsert, conferring a symmetry to the calice. The paliform lobes (incorrectly called pali by Cairns 1982) are tall slender ribbons sometimes occurring two to a septum, but often missing from all or some of the septa within a calice. The paliform lobes (P3) are indistinguishable from the centrally placed columellar elements, altogether forming a robust axial structure.
The normally extratentacular (sympodial) budding of this species is usually sufficient to distinguish it from the only other colonial scleractinian known from this region, Solenosmilia australis , which has consistently distomadeal intratentacular budding. But, on rare occasions, B. candida is known to have this type of budding as well ( Fig. 2A View FIGURE 2. A – C ). In that case, B. candida can be distinguished by its large columella, paliform lobes (P3), and finely dentate septal axial edges.
Dead coralla of this species form the substrate for at least six species of solitary Scleractinia and many other encrusting organisms (see Material). The species occurs in such local abundance ( Fig. 1A View FIGURE 1. A ) that it must be considered to be a framework-forming (or constructional) azooxanthellate species, along with 18 other species discussed by Roberts et al. (2009: Table 2.3). The tissue of the living coral is pale orange.
Distribution. Southernmost Brazil (off Rio Grande), entire coast of Argentina to latitude of Bahía Desvelos, and off Peninsula de Taito, Chile ( Fig. 5), 500–1626 m. Previously known only from the holotype and nine additional records (Cairns 1982), the numerous specimens reported herein add many records of this species from off Argentina, and slightly increase its deepest known depth range from 1250 to 1626 m. B. candida is one of the few species to occur in cold temperate as well as the southern warm temperate region of the western Atlantic. It is also noteworthy in occurring on both sides of Patagonia.
Material: PAT0108DR1, 10, MNCN; PAT0108DR2, 10, MNCN; PAT0108DR7, 10, MNCN; PAT0108DR8, 1, MNCN; PAT0108DR11, 5, MNCN, and as dead substrate for M. capitolii , USNM; PAT0108DR12, 10, MNCN; PAT0108DR15, 5, MNCN, and as dead substrate for F. cinctutum , USNM 1193314; PAT1008DR1, 3, MNCN; PAT1008DR4, 5, MNCN; PAT1008DR5, 5, MNCN, and 1 calice, USNM 1193268; PAT1008DR6, 3, MNCN; PAT1008DR9, 2, MNCN; PAT1008DR10, 1, MNCN; PAT1008DR13, 5, MNCN; PAT1008BC24, 1 as dead substrate for Javania cristata , USNM 1193330; PAT1108DR3, 3, MNCN; PAT1108DR4, 5, MNCN and 1 colony, USNM 1193271; PAT1108DR8, 2, MNCN; PAT1108DR9, 10, MNCN; PAT1108DR11, 3, MNCN; PAT1208DR4, 5, MNCN; PAT1208DR5, 5, MNCN; PAT 1208DR6, 5, MNCN; PAT1208DR7, 5, MNCN; PAT1208DR9, 4, MNCN; PAT1208DR10, 5, MNCN; PAT1208DR11, 5, MNCN; PAT1208DR14, 3, MNCN; PAT1208DR16, 5, MNCN; PAT0209DR1, 5, MNCN; PAT0209DR2, 3, MNCN; PAT0209DR3, 5, MNCN; PAT0209DR4, 5, MNCN; PAT0209DR5, 5, MNCN; PAT0209DR7, 5, MNCN; PAT0209DR8, 7, MNCN; PAT0209DR9, 4, MNCN; PAT0209DR10, 3, MNCN; PAT0209DR11, 3, MNCN and as dead substrate for D. dianthus , USNM 1192949; PAT0209DR12, 5, MNCN; PAT0209DR14, 5, MNCN and as dead substrate for C. cornu , USNM1193289; PAT0209DR15, 5, MNCN; PAT0209DR16, dead substrate for C. cornu , USNM 1193291; PAT0210DR5, 15, MNCN; PAT0210DR6, 10, MNCN; PAT0210DR7, 23, MNCN; PAT0210DR8, 10, MNCN; PAT0210DR9, 5, MNCN; PAT0210DR10, 1 colony, USNM 1193269; PAT0210DR11, 2, MNCN, and 2 branches, USNM 1193270; ATL08Lo17, 1, MNCN; ATL08Lo104, 10, MNCN; ATL09Lo8, 2, MNCN; ATL0310Lo32, 5, MNCN; ATL0310Lo94, 5, MNCN; WH 328/71, dead substrate for paratype of M. capitolii , USNM 83381.
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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