Abstract The Kasimovian Stage is the lower stage of the Upper Pennsylvanian Subsystem, in which a series of considerable biotic and abiotic events happened and changed the Earth. The Variscan orogeny and the Late Paleozoic Glaciation are two major events that caused geographical isolation of marine faunas and difficulties for a global correlation of biostratigraphy. Regional timescales of the Kasimovian across major continents are reviewed here. A global correlation of the Kasimovian is tentatively established based on a detailed review of major fossil groups such as conodonts, fusulines and some macrofossils. The index taxon for the base of the Kasimovian Stage has not been selected. The conodont species Swadelina subexcelsa , Idiognathodus heckeli , I. turbatus and I. sagittalis have good potential. Among them, I . heckeli is considered the best marker for the base of the Kasimovian Stage because it can mark a bioevent in a wide geographical range, and more importantly, it has a clear taxonomic definition within a phylogenetic lineage. The fusuline Montiparus might be regarded as an auxiliary marker to define the base of the Kasimovian based on its wider distribution. Other proxies, i.e. isotopic dating and strontium, carbon and oxygen isotopic stratigraphy throughout the Kasimovian, are also reviewed. The Global Boundary Stratotype Section and Point (GSSP) candidates for the Kasimovian Stage include the Naqing section, South China, the Usolka section, South Urals and the Afanasievo section, Moscow Basin. The Naqing section is regarded as the most appropriate GSSP candidate in terms of its complete sedimentary succession, well-recorded conodont lineages and well-studied bio-, chemo- and cyclo-stratigraphy.

Abstract A threshold-like vegetational change in tropical wetlands occurred in the early Kasimovian (the US Desmoinesian–Missourian boundary) – Event 3. Two earlier significant changes occurred, first in the mid-Moscovian (Atokan–Desmoinesian; ∼Bolsovian–Asturian) – Event 1, and the second in the late Moscovian (mid-Desmoinesian; mid-Asturian) – Event 2. These changes occurred during a time period of dynamic and complex physical change in Euramerican Pangaea driven by changes in polar ice volume and accompanying changes in sea level, atmospheric circulation, rainfall, and temperature. During the Event 3 change, hyperbolized as ‘the Carboniferous rainforest collapse’, lycopsid dominance of (mostly peat) swamps changed to marattialean tree-fern and medullosan pteridosperm dominance, and biodiversity decreased. Event 3 encompassed one glacial–interglacial cycle and included vegetational turnover in other wetland habitats. For several subsequent glacial–interglacial cycles peatland dominance varied, known from palynology, before stabilizing. These vegetational changes likely reflect climatic events driving unidirectional, non-reversible wetland vegetational changes, during cooler, wetter parts of glacial–interglacial cycles. Discussion is complicated by different placements of crucial stratigraphic boundaries, but under the same names, compromising both clear communication and understanding of the literature. Not the least is the floating base of the Cantabrian Substage, together with the position of the Westphalian–Stephanian Stage boundary.

Abstract We present the first analysis of vegetational change in far western equatorial Pangaea (New Mexico, USA) during the Middle–Late Pennsylvanian transition (determined by conodonts and fusulinids) of the Late Paleozoic Ice Age. The study is based on the largest database assembled from this region: 28 of 44 quantitatively analysed floras from 14 of 26 stratigraphic levels. Most sampled floras are ‘mixed’, both below and above the boundary, including both hygromorphic and mesomorphic/xeromorphic taxa. The taxonomic data were recalibrated morphometrically focusing on foliar traits of lamina width and venation. All data were examined using stratigraphic credible intervals, capture–mark–recapture analyses, and resampling analyses. Results indicate no substantive taxonomic turnover across the boundary. This stands in marked contrast to patterns in mid-Pangaean coal basins where there is a large wetland vegetational turnover. However, plant and physical geological data indicate that immediately following the boundary in New Mexico, and for approximately half of the Missourian Stage, floras previously dominated by hygromorphs become overwhelmingly dominated by mesomorphic/xeromorphic taxa. Although expressed differently, the western Pangaean physical and palaeobotanical patterns parallel those from mid-Pangaean coal basins and suggest a widespread environmental change.

Abstract Late Pennsylvanian conodont faunas were dominated by idiognathodids historically assigned to Idiognathodus (flat P 1 ) or Streptognathodus (troughed P 1 ). Recent work suggests clades arose iteratively, through time, from unrelated ancestors in different geographical regions. The end-Desmoinesian extinction event terminated two major genera, Swadelina (troughed) and Neognathodus (long carina), and comparable new morphotypes developed from surviving Idiognathodus species in the early Kasimovian, especially in North America. True Streptognathodus (troughed) and Heckelina n. gen (asymmetric, eccentric groove) appeared in North America in the mid-Kasimovian. Another troughed clade arose in Eurasia (‘ S. ’ 2) and attained a global distribution by the late Kasimovian. A second, early Gzhelian, Eurasian radiation produced new troughed forms (‘ S. ’ 4) that dominated Gzhelian faunas globally. In South China, endemic clades of eccentrically grooved Idiognathodus ? and troughed forms (‘ S .’ 3) appeared in the late Kasimovian and persisted into the Gzhelian. Typical Idiognathodus species were uncommon by the late Kasimovian and disappeared in the mid-Gzhelian. After a low diversity interval in the mid-Gzhelian, a new major radiation of weakly troughed forms occurred (‘ S. ’ 5), which led to redevelopment of Idiognathodus -like elements in the Cisuralian. Other conodont genera from offshore ( Gondolella, Idioprioniodus ) and nearshore settings ( Hindeodus, Diplognathodus, Adetognathus, Ellisonia ) are poorly studied and show low diversity and little morphological change.