Megapora ringens ( Busk, 1856 )

Martino, Emanuela Di & Taylor, Paul D, 2012, Pyrisinellidae, a new family of anascan cheilostome bryozoans, Zootaxa 3534, pp. 1-20 : 16-18

publication ID

https://doi.org/ 10.5281/zenodo.213326

DOI

https://doi.org/10.5281/zenodo.6488418

persistent identifier

https://treatment.plazi.org/id/1373087C-FFD5-FFB7-C6A3-940823C5F0C3

treatment provided by

Plazi

scientific name

Megapora ringens ( Busk, 1856 )
status

 

Megapora ringens ( Busk, 1856) View in CoL

( Figs 39−44 View FIGURES 39 − 44 ; Table 6)

Lepralia ringens Busk, 1856: 308 .

Megapora ringens: Hincks, 1880: 172 View in CoL , pl. 22, fig. 1; Prenant & Bobin, 1966: 273; Ryland & Hayward, 1977: 107, fig. 47; Hayward & Ryland, 1998: 196 −199, fig. 58B −59.

Material examined. NHML 1911.10.1.629, Recent (specimen figured by Hincks, 1880, pl. 22, fig. 1), Shetland (Barlee), 80−170 fathoms. NHML 1911.10.1.631, Recent, Porcupine Bight, several encrusting three small pebbles.

Description. Colony encrusting, multiserial, unilaminar, developing small rounded patches. Pore chambers present, distal pore chamber slightly larger than distolateral pore chambers; pore windows oval (mean L = 37 µm, mean W = 10 µm), surrounded by a mural ring, that of the distal pore chamber facing frontally. Ancestrula oval and smaller than astogenetically mature autozooids (L = 223 µm, mean W = 166 µm); gymnocyst absent or hidden by later zooids, cryptocyst densely granular, occupying half of the frontal area, opesia trifoliate with two small oral spines (D = 12 µm) placed distally ( Fig. 44 View FIGURES 39 − 44 ). Autozooids in zone of early astogeny transitional in size and morphology between ancestrula and later autozooids ( Fig. 43 View FIGURES 39 − 44 ). Autozooids small, rounded hexagonal or oval, longer than broad (mean L/W = 1.27), separated by deep furrows. Gymnocyst narrow, slightly broader proximally. Cryptocyst extensive, coarsely and densely granular, depressed centrally, submarginally raised to form a rounded ridge which together with distal rim of the opesia forms a pear-shaped outline on the frontal wall and around the opesia. Opesia strongly trifoliate, the proximal edge gently convex with rounded indentations at the proximolateral corners; a pair of rounded thick lateral denticles directed downwardly divide the larger, distal semicircular part of the opesia from the smaller but broader proximal part ( Fig. 41 View FIGURES 39 − 44 ). Oral spines numbering six, arranged in an arch around the distal edge of the opesia, the most proximal pair almost level with the denticles; distalmost pair of oral spines spaced more widely in ovicellate than non-ovicellate zooids. Complete ovicell not observed but that figured by Hayward & Ryland (1998, p. 197, fig. 58B) is hyperstomial, prominent, rounded and elongated, with a narrow, median triangular ectooecial window with thickened edges; a small rounded triangular kenozooid with a cryptocystal frontal area and a tiny central lacuna is present immediately distally of each ovicell ( Fig. 41 View FIGURES 39 − 44 ). Closure plates developed in some autozooids as distal extensions of the cryptocyst, with a small tuberculum located medially level with the proximal edge of the opesia, which is completely occluded ( Fig. 40 View FIGURES 39 − 44 ). Kenozooids of irregular shape frequently present along lateral margins of lobate colonies, slightly smaller (L = 258−291 µm, W = 195−218 µm) than autozooids; gymnocyst narrow but wider than in autozooids; cryptocyst coarsely and densely granular, continuous over the entire frontal area except for a small, round, lacuna (mean D = 25 µm) near the centre ( Fig. 42 View FIGURES 39 − 44 ). Avicularia absent.

Remarks. None of the material examined of this species had an intact ovicell; in all instances the roof of the ovicell was broken, revealing a floor consisting of an exterior skeletal wall with planar spherulitic microstructure delineating two lobes on either side of a median depression ( Fig. 41 View FIGURES 39 − 44 ). The presence of a small kenozooid distal of each ovicell, which is unique among the species described in this paper, recalls various other cheilostomes (e.g. Bishop & Househam 1987; Ostrovsky et al. 2008), and may signify evolutionary reduction of the zooid distal of the maternal zooid from an autozooid to a kenozooid.

Hayward & Ryland (1993) introduced the new genus Apiophragma for M. hyalina Waters, 1904 , referring to the shape of the mural rim from the Greek apios, a pear and phragma, a wall. Apiophragma resembles Megapora in its depressed cryptocyst, thick mural rim and distal arc of spines but differs in having only a weakly trifoliate opesia which is much smaller and narrowly bell-shaped, and the presence of opesiules. The inclusion of Apiophragma in the new family Pyrisinellidae should be considered after restudy of the type material of A. hyalina .

Distribution. Recent of boreal and arctic areas, widely distributed in the northeast Atlantic, extending southwards, in deep waters, as far as the Shetland Isles and Bergen, Norway ( Hayward & Ryland 1998).

N (colonies, zooids) Mean SD Range Zooid length 3, 30 414 39 367–489 Zooid width 3, 30 333 32 294–384 Orifice length 3, 15 100 13 82–116 Orifice width 3, 15 93 3 90–95 Ovicell length 2, 3 180 3 177–182 Ovicell width 2, 3 219 11 206–228

N, Number of colonies and number of zooids measured; SD, standard deviation.

NHML

Natural History Museum, Tripoli

Kingdom

Animalia

Phylum

Bryozoa

Class

Gymnolaemata

Order

Cheilostomatida

Family

Calloporidae

Genus

Megapora

Loc

Megapora ringens ( Busk, 1856 )

Martino, Emanuela Di & Taylor, Paul D 2012
2012
Loc

Megapora ringens:

Hayward 1998: 196
Ryland 1977: 107
Prenant 1966: 273
Hincks 1880: 172
1880
Loc

Lepralia ringens

Busk 1856: 308
1856
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