Agelas cerebrum Assmann
publication ID |
https://doi.org/ 10.11646/zootaxa.3794.3.1 |
publication LSID |
lsid:zoobank.org:pub:51852298-F299-4392-9C89-A6FD14D3E1D0 |
DOI |
https://doi.org/10.5281/zenodo.5691139 |
persistent identifier |
https://treatment.plazi.org/id/03F7DF34-C01A-FFD1-FF40-CB23DCF3EEEC |
treatment provided by |
Plazi |
scientific name |
Agelas cerebrum Assmann |
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Agelas cerebrum Assmann View in CoL , van Soest & Köck, 2001
Fig. 10 View FIGURE 10
Etymology from Latin, meaning brain; brain-like appearance.
Agelas cerebrum Assmann, 2000: 37 View in CoL , pl. 2; Assmann et al., 2001: 361, Fig. 1 View FIGURE 1 ; Zea et al., 2009. Agelas conifera View in CoL ; Alcolado, 2002: 61 (in part).
[Non: Agelas conifera ( Schmidt, 1870) View in CoL (a valid species)]
Material and distribution. Holotype examined at the Zoölogisch Museum Amsterdam ( ZMA – POR 15603), collected at the deep reef slope of Chub Cay, Bahamas, 32 m. The material reviewed here (INV– POR 925, 937) was also collected in the Bahamas.
This species seems restricted to the Bahamas area (see also Assmann 2000; Zea et al. 2009) and Cuba ( Alcolado 2002). Therefore, we consider it as a Bahamian-Greater Antilles species. Our specimens were found from 12 to 18 m in depth, abundant at 14– 15 m.
Description. Shape as robust tubes, often as thick as barrels or vases, single or in groups, sometimes laterally fused. Height up to 25–35 cm, diameter up to 12–16 cm (single tube, Fig 10 View FIGURE 10 A) or 22–30 cm (fused tubes, Fig 10 View FIGURE 10 B). Pseudoscula 3–6 cm in diameter, collared by a narrow (5–8 mm, Fig 10 View FIGURE 10 C) membrane, opening into atria with a rather constant diameter throughout its depth. The external colour can be salmon to light reddish brown; internal colour orange to brownish orange; when dry the colour becomes light reddish brown. Pinacoderm sustained by tracts of spicules protruding from main fibres.
The external surface is rough and characteristically convoluted throughout the surface ( Fig 10 View FIGURE 10 D); the convolutions are 2–8 cm long, 2–3 cm wide and 4–5 cm deep, longer when connected to each other; isolated ones with a key-hole or kidney aspect; internal wall of the convolutions is lined by a thick bright membrane similar to the internal membrane of the atrium. The surface is even in a ring around pseudoscula. Oscules 0.5–1.5 cm in diameter, scattered along the atrium internal walls. The central area of the external convolutions have scattered tiny round oscules (<1.2 mm) conspicuous in dry specimens. Consistency in life is strongly spongy but tough, almost incompressible; when dry it becomes harder. Choanosome is dense with channels 5–10 mm in diameter.
Skeleton composed of echinated and heavily cored (5–9 spicules per cross section) primary fibres (80–170 µm in diameter), echinated and not cored secondary fibres (50–90 µm in diameter) and rarely echinated tertiary fibres (30–60 µm in diameter). The acanthostyles are straight with 5–7 spines per whorl; length 72–167 (115±21.9) µm, width 3–10 (7±1.4) µm and 8–20 (13±2.5) whorls per spicule. Detailed lengths, widths and average number of whorls are shown in Table 2.
Remarks. This species usually grows in deep exposed areas. Dr. P.M. Alcolado (pers. comm.; Alcolado 2002) believes that A. conifera , A. tubulata and A. cerebrum are variations of the same species (vis. A. conifera ). However, here we keep these species separate from predominant morphological characteristics which can be ascertained when one compares in the field co-existing individuals. In the Bahamas, A. cerebrum is easily identified underwater by its notable salmon colour (different from the other local Agelas ) and remarkably convoluted aspect of the external surface. At San Andres Island, some rather thick tubes of A. tubulata have portions of the surface with deep crevasses, which resemble those of A. cerebrum . A. tubulata can be distinguished by its brownish to orange colour, longer spicules, and by the absence of small round oscules in the interconvolution areas, when these occur. Perhaps these convolutions are simply the result of growth adjustments when body walls thicken, in order to maintain enough irrigation through the aquiferous system (P.M. Alcolado, pers. comm.). However, the absence of small round oscules in thick, crevassed specimens of A. tubulata argues against this. P.M. Alcolado (pers. comm.) has found A. cerebrum in Cuba as robust, single or laterally fused tubes, or large single or grouped cones fused at the base (with a large oscule on the top), at depths of about 15 to 20 m; colour, medium brown.
We compared the holotype of A. cerebrum and our material with the holotype A. conifera , and although spicule sizes slightly overlap (also mentioned by Assman et al. 2001), the distinctive shape of A. cerebrum (barrel/vaselike tubes plus deep grooves and convolutions) separate it from A. conifera (branch with cones wider than taller). Whether these differences are ecological or species specific, remains to be determined. The record of Assmann (2000) gives photos of this species but not a description; being an unpublished thesis from which the complete description was made, it is not taxonomically valid as to have priority.
ZMA |
Universiteit van Amsterdam, Zoologisch Museum |
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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Agelas cerebrum Assmann
Parra-Velandia, Fernando J., Zea, Sven & Van Soest, Rob W. M. 2014 |
Agelas cerebrum
Alcolado 2002: 61 |
Assmann 2001: 361 |
Assmann 2000: 37 |