Abstract: This review has been undertaken in order to present some interpretations about the biostratigraphy of the smaller foraminifers belonging to four classes present during the Permian: Fusulinata, Miliolata, Nodosariata and Textulariata. Biostratigraphic markers of these classes are principally known in the orders and superfamilies of Lasiodiscoidea, Bradyinoidea and Globivalvulinoidea (Fusulinata), Cornuspirida (Miliolata), and in the entire class Nodosariata. The class Textulariata is too little known during the Permian to play a significant biostratigraphical role: nevertheless, the appearance of the order Verneulinida is probably an important bioevent. The main genera among the lasiodiscids are Mesolasiodiscus , Lasiodiscus , Lasiotrochus , Asselodiscus , Pseudovidalina , Xingshandiscus and Altineria ; the bradyinoids Bradyina and Postendothyra ; the globivalvulinoids Globivalvulina , Septoglobivalvulina , Labioglobivalvulina , Paraglobivalvulina , Sengoerina , Dagmarita , Danielita , Louisettita , Paradagmarita , Paradagmaritopsis and Paremiratella ; the miliolates Rectogordius , Okimuraites , Neodiscus , Multidiscus , Hemigordiopsis , Lysites , Shanita and Glomomidiellopsis , and the tubiphytids and ellesmerellids, which might be specialized miliolate and cyanobacterium consortia, with reference to microstructures and phylogenies of these groups. The Nodosariata markers belong to Nodosinelloides , Tezaquina , Polarisella , Geinitzina , Pachyphloia , Rectoglandulina , first true Nodosaria , Langella , Pseudolangella , Calvezina , Cryptoseptida , Cylindrocolaniella , Colaniella , Frondina and Ichthyofrondina , but their lineages are too poorly understood to permit an accurate biostratigraphic use at the present time. The superfamily Geinitzinoidea is emended. Finally, palaeobiogeographical implications based on Shanita , Colaniella and Altineria are given.

Abstract: The Permian timescale has developed over about two centuries of research to the current chronostratigraphic scale advocated by the Subcommission on Permian Stratigraphy of three series and nine stages: Cisuralian (lower Permian) – Asselian, Sakmarian, Artinskian, Kungurian; Guadalupian (middle Permian) – Roadian, Wordian, Capitanian; and Lopingian (upper Permian) – Wuchiapingian and Changhsingian. The boundaries of the Permian System are defined by global stratotype sections and points (GSSPs) and the numerical ages of those boundaries appear to be determined with a precision better than 1‰. Nevertheless, much work remains to be done to refine the Permian timescale. Precise numerical age control within the Permian is very uneven and a global polarity timescale for the Permian is far from established. Chronostratigraphic definitions of three of the nine Permian stages remain unfinished and various issues of marine biostratigraphy are still unresolved. In the non-marine Permian realm, much progress has been made in correlation, especially using palynomorphs, megafossil plants, conchostracans and both the footprints and bones of tetrapods (amphibians and reptiles), but many problems of correlation remain, especially the cross-correlation of non-marine and marine chronologies. The further development of a Permian chronostratigraphic scale faces various problems, including those of stability and priority of nomenclature and concepts, disagreements over changing taxonomy, ammonoid v. fusulinid v. conodont biostratigraphy, differences in the perceived significance of biotic events for chronostratigraphic classification and correlation problems between provinces. Future research on the Permian timescale should focus on GSSP selection for the remaining undefined stage bases, the definition and characterization of substages, and further development and integration of the Permian chronostratigraphic scale with radioisotopic, magnetostratigraphic and chemostratigraphic tools for calibration and correlation.

Abstract Quantitative analysis of Oligocene assemblages in cool-water carbonates suggests a two-tiered response by benthic, neritic foraminiferal faunas to a succession of glacioeustatic fluctuations. One response appears at lower-frequency or second-order cycles and is marked by more substantial, nonreversible, taxic change at the Eocene–Oligocene boundary, at the Rupelian–Chattian (Early–Late Oligocene) boundary, and during a Late Oligocene transgressive phase. These faunal changes were responses to climatic changes forced by glaciations signaled by oceanic oxygen-isotope maxima. The second response is seen in fluctuations in the abundances of benthic neritic taxa. Rapid changes in infaunal-to-epifaunal ratios appear to chronicle reversible “short-term” local paleoenvironmental shifts forced by third-order cycles. Sequence stratigraphic packages and bounding surfaces are easier to decipher in sequences characteristic of the warmer and more sluggish Priabonian ocean than in the cooler and better-ventilated Rupelian ocean. The major (second-order) physical event at the Rupelian–Chattian boundary is recorded faunally but shows a relatively muted impact on the regional succession of neritic foraminifera compared to the sequence boundary coinciding with glaciation Oi1 in the very earliest Oligocene. We interpret, from graphic correlation and cluster analysis, that patterns of faunal change reflect endemism that developed on a broad neritic zone with wide variation in intensity of oceanic influence.