Abstract: The most extensive Permian tetrapod (amphibian and reptile) fossil records from the western USA (New Mexico to Texas) and South Africa have been used to define 11 land vertebrate faunachrons (LVFs). These are, in ascending order, the Coyotean, Seymouran, Mitchellcreekian, Redtankian, Littlecrotonian, Kapteinskraalian, Gamkan, Hoedemakeran, Steilkransian, Platbergian and Lootsbergian. These faunachrons provide a biochronological framework with which to assign ages to, and correlate, Permian tetrapod fossil assemblages. Intercalated marine strata, radioisotopic ages and magnetostratigraphy were used to correlate the Permian LVFs to the standard global chronostratigraphic scale with varying degrees of precision. Such correlations identified the following significant events in Permian tetrapod evolution: a Coyotean chronofaunal event (end Coyotean); Redtankian events (Mitchellcreekian–Littlecrotonian); Olson’s gap (late Littlecrotonian); a therapsid event (Kapteinskraalian); a dinocephalian extinction event (end Gamkan); and a latest Permian extinction event (Platbergian–Lootsbergian boundary). Problems of incompleteness, endemism and taxonomy, and the relative lack of non-biochronological age control continue to hinder the refinement and correlation of a Permian timescale based on tetrapod biochronology. Nevertheless, the global Permian timescale based on tetrapod biochronology is a robust tool for both global and regional age assignment and correlation. Advances in Permian tetrapod biochronology will come from new fossil discoveries, more detailed biostratigraphy and additional alpha taxonomic studies based on sound evolutionary taxonomic principles.

Abstract: Conchostracans are one of the most common fossil animal groups of continental deposits from late Palaeozoic to modern times. Their habitats have ranged from perennial lakes of the Carboniferous and Early Permian to seasonal playa lakes and temporary ponds from the late Early Permian into the Triassic, where they could form mass occurrences. This, together with relatively high speciation rates, makes them ideal guide fossils, especially in otherwise fossil-poor wet and dry red beds. Based on material and data collected since the 1980s from both surface outcrops and well cores in central Europe, a preliminary conchostracan zonation is proposed. We used a conservative approach, erecting assemblage zones comprising two or three species instead of species-range zones with only one or, sometimes, two forms. Assemblage zones are more robust and provide more reliability for each delineated time interval. Isotopically dated occurrences of conchostracan zone species, or co-occurrences of conchostracans, insect zone species and marine index fossils such as conodonts and fusulinids, allow us to correlate our assemblage zones with the marine Standard Global Chronostratigraphic Scale.

Abstract An assemblage of the burrowing ghost shrimp, Protocallianassa faujasi , is described, providing the first evidence of this decapod species from Sweden. The fossils occur in successions of the informal earliest late Campanian Belemnellocamax balsvikensis zone at Åsen and the latest early Campanian B. mammillatus zone at Ivö Klack, both in the Kristianstad Basin of NE Skåne. Numerous, heavily calcified chelipeds were found within a restricted bed at Åsen that was rich in carbonate-cemented nodules. Based on the burrowing lifestyle of modern mud shrimps, we interpret these nodules as infilled burrow chambers. The low abundance of molluscs within the Protocallianassa beds is also consistent with analogous extant communities, indicating that a similar ecologically exclusive relationship ruled within the Late Cretaceous shallow-marine ecosystems.

Patterns of diversification and longevity in Paleogene coccolithophorids are analyzed by combining the temporal history of selected genera, families, and orders with the number of discrete morphospecies in them. The coccolithophorids underwent an abrupt mass extinction at the Cretaceous/Paleogene boundary, and a rapid (~1 m.y.-long) global turnover at the Paleocene/Eocene boundary. In contrast, they underwent a diachronous turnover at the Eocene/Oligocene boundary that spread over 6–7 m.y. at mid- and low-latitudes. The turnover included sequential extinctions and speciations of short-lived taxa, beginning slightly before 37 Ma, and losses of taxa that dominated mid- and low latitudes at 34.2 Ma and high latitudes at 32.3 Ma. It is also marked by a few evolutionary appearances, in particular, that of the Family Syracosphaeraceae, which is the most diversified of the living coccolithophorids. Most importantly, the turnover resulted in a shift in the balance between families across several orders, such that families that dominated during the Eocene dwindled during the turnover, and, conversely, families that were little diversified during the Eocene became dominant. Thus, members of Family Coccolithaceae and the genus Heliodiscoaster typify Eocene communities; members of the Family Calcidiscaceae and the genus Eudiscoaster characterize Neogene communities. This shift was accompanied by a decrease in the robustness of coccoliths, suggesting that the Eocene/Oligocene event had a marked effect on the physiology of Eocene coccolithophorids. Bolide impacts and the emplacement of large basaltic provinces provide mechanisms to explain large biotic events. Such mechanisms, however, can be ruled out in the case of the Eocene/Oligocene turnover, which was undoubtedly related to climatic cooling and glaciation. The filtering effect of environmental stress on late Eocene diversity remains to be explained.