Michelinia de Koninck, 1841

Fedorowski, Jerzy, Bamber, E. Wayne & Richards, Barry C., 2021, Mississippian colonial tabulate and rugose corals from the Flett Formation, Liard Basin, northwest Canada, Acta Palaeontologica Polonica 66 (3), pp. 679-704 : 687-689

publication ID

https://doi.org/ 10.4202/app.00817.2020

persistent identifier

https://treatment.plazi.org/id/AD2B443B-9809-FFD3-9BFA-C3CD9E2DB96D

treatment provided by

Felipe

scientific name

Michelinia de Koninck, 1841
status

 

Genus Michelinia de Koninck, 1841 View in CoL

Diagnosis.—See Hill (1981: F561).

Remarks.—Colonies included here in the Michelinia de Konnick, 1841 , belong to a morphologically complex group of species developing both tabulae and abundant dissepiments. That morphological complexity led Stumm (1948) to introduce the new genus Tabellaephyllum Stumm, 1948 , based on the new species T. peculiare Stumm, 1948 , and to include it in the Rugosa. Oliver and Sando (1977) rejected both the Devonian age of T. peculiare and its position within the Rugosa, identifying that species as belonging to the tabulate genus Michelinia . Also, they suggested the synonymy of T. peculiare with Michelinia expansa White, 1883 , “a common and widespread element of the Early Mississippian … coral fauna…” as mentioned by Oliver and Sando (1977: 422). However, Lafuste and Plusquellec (1990) cast doubt on the identification of “ M. expansa ” as Michelinia by placing that generic name in inverted comas as far as the topotypes of that species are concerned. They identified Michelinia expansa of Sando (1969a) as Turnecipora sp. and in the case of Tabellaephyllum peculiare concluded: “The beautiful wording of Oliver and Sando suits us perfectly ‘ Tabellaephyllum Stumm is a Michelinia ’ however, silicification of the wall precludes precise attribution to a genus.” (“La belle formule de Oliver et Sando (1977) nous agrée parfaitement ‘ Tabellaephyllum Stumm is a Michelinia ’ mais la silicification de la muraille empêche toute attribution générique precise”) ( Lafuste and Plusquellec 1990: 23). The morphology of the intercorallite walls, observed in fragments of two colonies ( Figs. 7A View Fig 2 View Fig , 8C View Fig 3 View Fig ), suggest they are related to Turnecipora Lafuste and Plusquellec, 1985, whereas the microstructure of the walls in the remaining parts of those colonies and in the other two colonies were destroyed by recrystallization with only the darker middle line recognizable. Thus, our suggestion is not supported firmly, precluding a further discussion of that matter and our genus and species identifications rely on the general morphology of the coral skeletons.

Michelinia expansa White, 1883

Figs. 7 View Fig , 8 View Fig .

Material.— Four almost complete colonies ( Fig. 6 View Fig ) from the Flett Formation , Rundle Group , Liard Basin , Northwest Territories, Canada: IG-17 = UAM-Tc.Can./1, Tlogotsho Member (70 m above base), lower Viséan; IG-91-1 = UAM-Tc. Can/2, IG-91-2 = UAM-Tc.Can/3, IG-93 = UAM-Tc.Can/4, Meilleur Member (270 m above base and 50 m above base of member), middle Viséan. Peripheral parts of colonies, i.e., holotheca and fragments of external corallites corroded. Corallite skeletons recrystallized, partly dolomitized and/or replaced by silica. Microstructure of wall destroyed in most. Septal spines extremely rare and may have been dissolved. Corallite calices preserved in fragments of two colonies .

Description.—Colonies hemispherical, cerioid as documented by tripartite composition of inter-corallite walls ( Fig. 8C View Fig ), i.e., partition of Fedorowski and Jull (1976). Corallites within colonies differentiated in size into a few large corallites and many smaller corallites, surrounding large ones ( Figs. 7A View Fig 1 View Fig , 8B View Fig 2 View Fig ). Diameters of largest corallites: 6.5 mm in specimens UAM-Tc.Can./1, 3 and 7.5 mm in colonies UAM-Tc.Can./2, 4. Pattern described suggests either differentiated preferences in offsetting with only some polyps within colony being able to offset, or ability to offset appearing late in polyps growth. Offsetting lateral ( Fig. 8A View Fig 2 View Fig , B 1, C 1 View Fig , C 2 View Fig , C 4 View Fig ). Offsets separated by partitions early in their growth, but a communication duct or pore connecting parental polyp and its offset recognizable at very beginning of offsetting when longitudinal section centric (e.g., Fig. 8A View Fig 2 View Fig , arrows; B 1, grey arrows). Such communication apparently absent when section eccentric ( Fig. 8B View Fig 1 View Fig , black arrow) and can be missing from transverse section ( Fig. 8C View Fig 1 View Fig ). Pores of early growth stage of one offset open towards two mature corallites ( Fig. 8C View Fig 4 View Fig ) recognized as well. Also, pores connecting offset with adjacent corallites common ( Fig. 8A View Fig 2 View Fig , arrows; B 1, grey arrows). Septal spines extremely rare, very small when present ( Fig. 7A View Fig 3 View Fig ). Pores connecting mature corallites rare, but both types (P 1 and P 2) documented; sometimes both types occurring close to one another ( Fig. 7A View Fig 4 View Fig ). Dissepiments absent from young corallites ( Figs. 7A View Fig 1 View Fig , 8C View Fig 1 View Fig , C 2 View Fig , C 4 View Fig ), growing in number from one row in small corallites to 2–4 rows in large corallites. Long, steeply down sloping dissepiments may occupy up to 1/2 corallite lumen. Only complete tabulae, expanding through entire corallite lumen, present during several millimeters of earliest corallite growth. In mature corallites tabulae vary from horizontal or slightly sagging to convex; all observed in same colony or even same corallite ( Figs. 7A View Fig 1 View Fig , upper, 8A 2, B 1).

Remarks.—Doubts expressed above in the remarks on the genus resulted in both, removal from the synonymy and identification of species based on the macro-morphology. Also, a wide intraspecific variability is here accepted rather than attempting to identify the colonies as different species. Such characters as “thinner walls and fewer and generally more convex tabulae” listed by Sando (1969a: 311) as the only characters distinguishing M. leptosphragma Armstrong, 1962 , from M. expansa are here considered inadequate for distinction between species. Thickness of walls may vary ( Fig. 8C View Fig 2 View Fig , C 5). Thus, the synonymy of those two seems very probable. All colonies described here resemble both “ Tabellaephyllum peculiaris Stumm, 1948 ”, ( Stumm 1948: pl. 12: 1, 2, 9, 11; Lafuste and Plusquellec 1990:fig.6)and the type and topotype specimens of Michelinia expansa White, 1883 ( White 1883: pl. 39: 2a, b; Sando 1969a: pl. 39: 1–3; Lafuste and Plusquellec 1990: fig. 7a, b). They differ clearly from Michelinia meekiana Girty, 1910 ( Girty 1910: 189 only; Sando 1969b: pl. 2: 6–9; Plusquellec and Sando 1987) in possessing short tabulae but dissepiments common, long and steeply sloping down.

Stratigraphic and geographic range.—Viséan (Mississipian, Carboniferous), Flett Formation, Rundle Group, Liard Basin, Northwest Territories, Canada; known also from Shunda Formation, Rundle Group, Liard Basin, Northwest Territories, Canada; Chouteau Limestone, Missouri; Redwall Limestone, Arizona; Lodgepole Formation, Utah; all upper Tournaisian (Mississipian, Carboniferous).

Kingdom

Animalia

Phylum

Echinodermata

Class

Echinoidea

Order

Echinolampadacea

Family

Laganidae

Loc

Michelinia de Koninck, 1841

Fedorowski, Jerzy, Bamber, E. Wayne & Richards, Barry C. 2021
2021
Loc

Michelinia expansa

White 1883
1883
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