Stelechophyllum Tolmachev, 1933
publication ID |
https://doi.org/ 10.4202/app.00817.2020 |
persistent identifier |
https://treatment.plazi.org/id/AD2B443B-9815-FFCF-9833-C3719E3CBF5D |
treatment provided by |
Felipe |
scientific name |
Stelechophyllum Tolmachev, 1933 |
status |
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Genus Stelechophyllum Tolmachev, 1933
Remarks.—The diagnosis of this genus emended by Sando (1983: 9) is too detailed in such characters as two orders of septa, common for the entire suborder and incomplete in such an important character as the microstructure of septa. We accepted it here on the condition of being temporary. The same is true for the geographical distribution and the species content of that genus suggested by Sando (1983). Unfortunately, the single colony available for this study cannot form the basis for a comprehensive discussion.
Stelechophyllum cf. banffense ( Warren, 1927) Fig. 16 View Fig .
Material.— Fragment of cerioid colony C-52434 = GSC 142476 View Materials , ca. 90×70× 80 mm in size from Flett Formation undivided, Viséan , Rundle Group , Liard Basin, Northwest Territories, Canada. Some corallites strongly re-crystallized (see below) .
Description. —Maximum number of septa measured—18 with n:d value 18:7.8×6.1 mm. Most common number of septa is 17 with corallite diameters 7.1×6.1 mm, 9.0×6.0 mm. Morphology of corallites varies greatly as a result of diagenetic alteration. Most altered corallites form a belt surrounding less altered part of the colony ( Fig. 16 View Fig , arrows). Boundary between those two fragments crosses several corallites as indicated by their morphology. Parts of corallites adjacent to less altered sectors of colony closely resemble corallites from that sector, whereas their opposite parts look like corallites from the diagenetically altered sector. In parts of colony showing least diagenetic alteration, major septa thin, long, approaching and some meeting thin pseudocolumella, commonly connected to both protosepta. Minor septa thin, in full number, all enter tabularium. Dissepiments mostly interseptal, regular. Lonsdaleoid dissepiments small when present. In corallites most altered diagenetically, either all, or most major septa restricted to tabularium. Minor septa very restricted in number. Few of them remain as thin, spike-like bodies attached to external walls, mostly absent. Dissepimentarium consists solely or mostly of large lonsdaleoid dissepiments, some surrounding more than 1/4 corallite diameter. Pseudocolumellae either absent from diagenetically most advanced corallites or free when surviving. Dissepiments in longitudinal sections either in one vertical row ( Fig. 16A View Fig 5) or up to three, gently dipping rows ( Fig. 16A View Fig 2 View Fig ). Tabulae complete or incomplete, deflected gently from thin pseudocolumella. Some tabellae rest upon underlying tabulae. Increase lateral ( Fig. 16A View Fig 3 View Fig , A 4 View Fig , A 6 View Fig , A 7 View Fig ). Acolumellate early growth stage of offsets continue up to their total separation from parental polyp ( Fig. 16A View Fig 6 View Fig ). Derivation of pseudocolumella from axial septum very probable, but diagenetic alterations precludes firm recognition of that process ( Fig. 16A View Fig 7 View Fig ).
Remarks.—The morphology of the colony under discussion differs from the lectotype ( Nelson 1960: pl. 23: 4, 5; Bamber 1966: pl. 3: 5) in its n:d value, in having stronger minor septa in its less altered part and in having a weaker pseudocolumella. It resembles small and simple variants of S. banffense ( Warren, 1927) , characterized by Sando (1983: 13) as “highly variable species”. Differences in the morphology illustrated by Sando (1963: pls. 8, 9) may have resulted from a differentiated intensity in diagenetic alterations. His colonies with large lonsdaleoid dissepiments and reduced minor septa may correspond to more altered parts of the colony described above, whereas those with the minor septa well developed and the lonsdaleoid dissepiments are rare and may correspond to the less altered part of that colony ( Sando 1983: pl. 8: 1, 3 and pl. 9: 1, respectively). The longitudinal section illustrated by Sando (1983: pl. 4: 2c) resembles that illustrated here ( Fig. 16A View Fig 2 View Fig , A 5). It is probable that those two corallites are conspecific. The question is whether they can be included within the limits of intraspecific variability of S. banffense or should be described as new. Having such restricted material, taking in mind the large variability of the specimens included in S. banffense so far, and considering the influence of diagenesis on the morphology of the corals documented above, the conformity of the species described here to S. banffense is the safest solution.
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