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EN
Several specimens derived from the Missourian (Pennsylvanian) deposits of the Glass Mountains (SW Texas, USA) are identified as Yuanophylloides Fomichev, 1953. Some species that earlier authors included in the genera Campophyllum Milne-Edwards and Haime, 1852, Bothrophyllum Trautschold, 1879, and Neokoninckophyllum Fomichev, 1939 are re-identified as belonging to Yuanophylloides. In addition to the type genus, a new subgenus Patulaxis of Yuanophylloides with the type species Y. (P.) molestus sp. nov. and the new species Y. (P.) parcus and Y. (P.) laxus are introduced. Re-identification of the upper Serpukhovian Campophyllum kansasense Miller and Gurley, 1893 as Yuanophylloides renders untenable the origin of that genus in the Donets Basin. The circum-Laurussia warm current is suggested as having carried Yuanophylloides larvae from the North American superprovince to the Paleotethyan superprovince. This genus supplements the group of genera suggested by Fedorowski (2023) as having originated in the North American superprovince and migrating to the Paleotethyan superprovince. Together, these genera demonstrate the importance of taxonomic investigation to establish paleobiogeography as a constrain on global (i.e., tectonic scale) environmental reconstructions.
EN
The paper focuses on the taxonomic description of the lower Carboniferous (uppermost Tournaisian to middle Viséan) solitary rugose corals from bedded limestone and shale units in the Flett Formation in the Jackfish Gap (eastern Liard Range), northwestern Canada. The corals described herein include 12 species representing the genera Ankhelasma Sando, 1961, Bradyphyllum Grabau, 1928, Caninophyllum Lewis, 1929, Cyathaxonia Michelin, 1847, Ekvasophyllum Parks, 1951, EnniskilleniaKabakovich in Soshkina et al., 1962, Vesiculophyllum Easton, 1944 and Zaphrentites Hudson, 1941. Two of these species are new (Ankhelasma canadense sp. nov. and Ekvasophyllum variabilis sp. nov.) and 6 taxa are described in open nomenclature. The distribution and relative abundance of solitary Rugosa in Europe and the Liard Basin confirm the geographical proximity of those areas and the open marine communication between them during the early Carboniferous. It therefore represents an important contribution to the determination of the time of isolation of the western Laurussia shelf fauna from that of southeastern Laurussia, as well as the time of the possible emergence of species from southeastern Laurussia into the western Laurussia seas. Of particular importance here are cosmopolitan taxa and the timing of their disappearance from the fossil record.
EN
A detailed analysis of the upper Viséan, Serpukhovian and Bashkirian Rugosa of the Donets Basin confirms their Mississippian/Pennsylvanian turnover during the Eumorphoceras / Homalophyllites-Hudsonoceras Zone, as postulated earlier (Fedorowski 1981a). The deterioration of rugose corals, globally diverse in time and space in the late Viséan and Serpukhovian, has resulted in the patchy distribution of survivors and newcomers, present in the Bashkirian. Difficulties in inter-basinal communication and the isolation of some sites have resulted in a different content of Bashkirian Rugosa in particular patches, with only rare genera in common. New data has made it possible to document the appearance of the first late Carboniferous genera in the Donets Basin as early as the lower Voznessenkian Horizon (= lower Chokierian Substage), i.e., close to the beginning of the Bashkirian Stage. The two stages of diversification, established in the Bashkirian rugose corals of the Donets Basin, cannot find their counterparts elsewhere. A palaeogeographic overview of the most important sites of diversified rugose corals documents the need to re-examine many taxa, which should be based on complete specimen studies. This and the precise placement of taxa in the modern stratigraphy must be done in order to make rugose corals globally comparable. Simple repetitions of names, commonly used in general summaries, is strongly misleading in both stratigraphic and palaeogeographic reconstructions.
EN
Inconsistency in the approach to the corals included by different authors in the families Tachylasmatidae Grabau, 1928 and Pentaphyllidae Schindewolf, 1942 are discussed in the context of their relationship vs homeomorphy to the Family Plerophyllidae Koker, 1924. Following Schindewolf (1942), the pentaphylloid or cryptophylloid early ontogeny, typical of the former two families, is contrasted with the zaphrentoid ontogeny typical of the latter family. Comprehensive analysis proves the independent taxonomic position of the Suborder Tachylasmatina Fedorowski, 1973. The taxa described herein support this idea. The relationship of the two families: Tachylasmatidae and Pentaphyllidae within the framework of this suborder are suggested. A new genus left in open nomenclature (represented by a single specimen) and three new species, Pentaphyllum sp. nov. 1, ? Pentaphyllum sp. nov. 2 and Gen. et sp. nov. 1 are described from lower Bashkirian deposits.
EN
The Family Kumpanophyllidae Fomichev, 1953, synonymised by Hill (1981) with the Family Aulophyllidae Dybowski, 1873, is emended and accepted as valid. The new concept of this family, based on both new collections and discussion on literature data, confirms the solitary growth form of its type genus Kumpanophyllum Fomichev, 1953. However, several fasciculate colonial taxa, so far assigned to various families, may belong to this family as well. The emended genus Kumpanophyllum forms a widely distributed taxon, present in Eastern and Western Europe and in Asia. Its Serpukhovian and Bashkirian occurrences in China vs Bashkirian occurrences in the Donets Basin and in Spain, may suggest its far-Asiatic origin, but none of the existing taxa can be suggested as ancestral for that genus. Thus, the suborder position of the Kumpanophyllidae remains unknown. Four new species: K. columellatum, K. decessum, K. levis, and K. praecox, three Kumpanophyllum species left in open nomenclature and one offsetting specimen, questionably assigned to the genus, are described.
EN
A new Subfamily Dirimiinae of the Family Kumpanophyllidae Fomichev, 1953 is introduced on the basis of Dirimia gen. nov., which is represented by six new named species and three species left in open nomenclature. The new species are Dirimia multiplexa, D. similis, D. recessia, D. composita, D. extrema, D. nana, Dirimia sp. 1, Dirimia sp. 2 and Dirimia sp. 3. The progressing atrophy of the columnotheca, leading to its total reduction in extreme species, and the occurrence of an axial structure instead of a compact pseudocolumella established in these species are accepted as differences exceeding the genus level. All specimens assigned to this subfamily were derived from the same Limestone F1 of the Donets Basin, and mostly from the same locality. The reasons for their split into a relatively large number of species are: 1) an increased radiation typical for faunal turnover times; 2) a delay in the appearance of differentiated skeletal characters relative to the appearance of genetic differences large enough to characterise different species; 3) a bias in preservation of fossil remnants by comparison to living populations, amplified by biases in the collections available for study by comparison to the total number of specimens fossilised.
EN
Two species, Antiphyllum sp. nov. 1 and Zaphrufimia sp. nov. 1, the first corals found in Štur horizon of the upper Malinowickie Beds, Upper Pendleian (E1), are here described. Additional study of the subspecies of Zaprufimia disjuncta show them to be more similar than previously thought. Although they occur mainly in the Enna and Barbara horizons, one specimen of Z. d. serotina comes from the Gabriela horizon. Biozone Zaphrufimia disujncta disjuncta/Z .d. praematura is proposed for the Enna and Barbara horizons. The subzone of Zaphrufimia/Triadufimia of that Biozone, defined by the presence of Triadufimia gen. nov., is restricted to the Enna horizon. As confirmed by the occurrence of Cravenoceratoides edalensis, the new subzone roughly corresponds to the E2b1 ammonite Zone. An Antiphyllum/Ostravaia/Variaxon assemblage Zone is proposed for the coral assemblage of the Gaebler horizon. Cravenoceratoides nitidus present in the Roemer band (Ib) shows it to correlate with the E2b2 ammonite Zone. Comparison with other European regions suggests possible faunal exchange between those areas and the Upper Silesian Coal Basin in Serpukhovian time.
EN
Cordibia pumila gen. et sp. nov. (Aulophyllidae, Dibunophyllinae) from the Lower Bashkirian E1 Limestone of the Donets Basin, Ukraine is described. The term "protocolony" is formally defined as a growth form intermediate between the solitary and colonial. Protocolonies consist of protocorallites and verticils of non-reproductive offsets [i.e., the lost structures]. The early ontogeny of a protocorallite is compared to the blastogeny in the same species in order to establish characters in common during both processes and to document the usefulness of blastogeny for phylogenetic reconstructions. The short duration and abundance of the occurrence (Limestones E1up acme, E11) of that species also makes it a good marker for the lowest Feninian (= Krasnopolyanian) strata in the Donets Basin.
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EN
Two genera from Upper Serpukhovian strata in the Czech Republic part of the Silesian Coal Basin are described and figured. Ostravaia gen. nov., included in Ostravaiainae subfam. nov., may belong to the Family Antiphyllidae Ilina, 1970. It is represented by one, morphologically variable new species, O. silesiaca. Two other species, conditionally included in that genus, are left in open nomenclature. Variaxon gen. nov., included in Variaxoninae subfam nov. of an undetermined family, is represented by two species, one of which, V. radians, is new.
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