‘Captorhinikos’ chozaensis Olson, 1954 is a captorhinid eureptile with multiple tooth rows from the lower Permian (Cisuralian: Kungurian) Clear Fork Group of north-central Texas and the Hennessey Formation of Oklahoma. It has five maxillary and four dentary tooth rows. We re-examined the available specimens referred to ‘Captorhinikos’ chozaensis to elucidate aspects of its skeletal structure and assess its phylogenetic relationships. Our parsimony analysis confirmed previous suggestions that this taxon is not referable to the same taxon as Captorhinikos valensis Olson, 1954 (type species of the genus) and ‘Captorhinikos’ parvus Olson, 1970 and thus is placed in its own new genus, Sumidadectes. It also recovered Sumidadectes chozaensis n. comb. as the earliest-diverging moradisaurine captorhinid.

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The Upper Cretaceous (Turonian) Bissekty Formation of Uzbekistan has yielded many isolated bones and teeth representing a variety of non-avian theropod dinosaurs. A pedal phalanx II-2 indicates the presence of a dromaeosaurid theropod that attained a larger body size than any previously known member of that clade. The same formation also yielded a large maxillary fragment that has recently been described as a neovenatorid carcharodontosaurian (Ulughbegsaurus uzbekistanensis). However, this specimen lacks unambiguously diagnostic features of that clade, and its purported carcharodontosaurian characters are either taphonomic artefacts or also shared by dromaeosaurids. Thus, the phylogenetic relationships of Uleghbegsaurus uzbekistanensis remain uncertain. A giant dromaeosaurid occurred together with the medium-sized tyrannosauroid Timurlengia euotica in the Bissekty assemblage.

The diversity of mid-Cretaceous tyrannosauroids is poorly understood. We describe a partial tyrannosauroid femur from the Albian–Cenomanian Wayan Formation of eastern Idaho that helps to fill in an important spatiotemporal gap in the North American record of tyrannosaurs. This specimen, consisting of the proximal half of the bone, is morphologically similar to the femur of Moros intrepidus, a small-bodied tyrannosauroid from the Cenomanian Mussentuchit Member of the Cedar Mountain Formation of Utah, but not referable to this taxon. The Wayan femur lacks an autapomorphy diagnostic for Moros intrepidus, indicating the presence of a previously unrecognized tyrannosauroid taxon in the early Late Cretaceous of Laramidia. Histological results indicate that, at the time of death, this individual was at least five years old, skeletally immature, and undergoing growth at a moderate rate. The addition of this tyrannosauroid to the Wayan-Vaughn Assemblage provides additional evidence for the widespread distribution of various tyrannosauroid taxa in Laramidia during the early Late Cretaceous.

Parioxys ferricolus Cope, 1878 is a long-neglected taxon of dissorophid temnospondyls from the early Permian (Cisuralian) of Texas. Reexamination of the original material and preparation of a previously undescribed specimen shed some light on the ontogeny and reveal numerous eucacopine features. P. ferricolus is characterized by: (1) a preorbital region 1.5 times as long as the posterior skull table in juveniles and twice as long in adults, (2) a parietal only two-thirds the length of the frontal, (3) interpterygoid vacuities shorter than half the skull length, (4) choanae posteriorly extended, and (5) vomer with enlarged, V-shaped median depression. P. ferricolus is found nested with Kamacops acervalis Gubin, 1980, with which it shares synapomorphies in the palate, within the dissorophid clade Eucacopinae.

A new taxon of sphenodontian reptile, Micromenodon pitti new genus new species is described from the Upper Triassic (Carnian) Vinita Formation of the Richmond basin of the Newark Supergroup in Virginia. It is diagnosed by a dorsoventrally deep facial process of the maxilla that extends for almost the entire anteroposterior length of the bone and by obtusely conical, strongly ribbed additional teeth in the maxilla that comprise a greatly enlarged tooth followed by smaller teeth posteriorly. Phylogenetic analysis found Micromenodon pitti n. gen. n. sp. as an early-diverging sphenodontian with fully acrodont tooth implantation. The maxillary dentition appears functionally suited for processing hard arthropod exoskeletons and snail shells.

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A new specimen of the basal mosasaur Halisaurus platyspondylus from the Severn Formation of Prince Georges County, Maryland (Upper Cretaceous: middle Maastrichtian) represents the most complete partial skeleton of this uncommon taxon to be described to date. The characteristic dorsoventral compression of the vertebral centrum is most pronounced in the anterior trunk vertebrae, and the centra of the posterior trunk vertebrae exhibit proportions more similar to those in other mosasaurs such as Plioplatecarpus. The postorbitofrontal forms its primary contact with the frontal rather than the parietal, and the supraoccipital is firmly attached to the ventral side of the parietal. The plane of articulation between the parietals and supratemporal is neither vertical (as in Varanidae) nor horizontal (as in Mosasauridae), but forms an angle of about 55 degrees with the horizontal. The quadrate bears a long, ventrally-flared suprastapedial process but appears to lack an infrastapedial process. Close similarities in the structure of the frontal and parietal with “Clidastes” sternbergii support referral of the latter to Halisaurus, but reference of Phosphorosaurus ortliebi to Halisaurus is questionable. Halisaurus has been recorded from the Santonian to the late Maastrichtian.

Dinnebitodon amarali, a new genus and species of Tritylodontidae, is described from the Early Jurassic Kayenta Formation of northeastern Arizona. It is distinguished from Kayentatherium wellesi by the possession of three (rather than one) upper incisors and upper postcanine teeth with two (rather than three) lingual cusps.

The stratigraphic framework for Triassic and Early Jurassic continental strata has greatly changed in recent years. These revised correlations necessitate a review of traditional views of early Mesozoic continental faunal succession and biogeography. We have examined the relationship between tetrapod distribution and paleogeographic context during the Triassic and Early Jurassic on the basis of a data base comprising updated faunal lists for major early Mesozoic assemblages of continental tetrapods. Analysis of these data supports the hypothesis that there were few barriers to biotic interchange among continental tetrapods throughout the Triassic and Early Jurassic. Early Mesozoic tetrapod assemblages are dominated by widely distributed, often cosmopolitan families. Late Triassic patterns of latitudinal variation among tetrapod assemblages appear to be correlated to those seen among terrestrial plants and contrast with the extremely uniform distribution of Early Jurassic continental biotas.

An incomplete skull of a small sphenodontian lepidosaur from the upper part of the Stormberg Group of southern Africa is referable to Clevosaurus Swinton, 1939. It is most closely related to C. bairdi from the McCoy Brook Formation (Lower Jurassic) of Nova Scotia (Canada) and C. mcgilli from the Dark Red Beds of the Lower Lufeng Formation (Lower Jurassic) of Yunnan (China). The new specimen is important because it represents the first record of Clevosaurus from the Southern Hemisphere. Like many other taxa of Early Jurassic continental tetrapods (crocodylomorph archosaurs, dinosaurs, synapsids), Clevosaurus had an apparently Pangaean distribution.

The first appearance of dinosaurs during the early Late Triassic coincided with marked faunal changes in terrestrial ecosystems. Most of the major groups of extant tetrapods (or their proximate sister-taxa), including mammaliaforms, crocodyliform archosaurs, lepidosaurs and turtles, also first appeared in the fossil record during the Late Triassic. On the other hand, a number of Palaeozoic ‘holdovers’, such as procolophonid parareptiles, dicynodont therapsids and many groups of temnospondyls, vanished near or at the end of the Triassic. The tempo and mode of this faunal turnover have long been debated, but there has been growing acceptance of a rather sudden event, although the precise dating of such an event remains controversial. However, new discoveries have cast doubt on this assumption. The persistence of non-dinosaurian dinosauromorphs alongside dinosaurs well into Norian times hints at a more protracted turnover. New data on Triassic insect assemblages indicate that turnover among insects may also have been more protracted and possibly not co-incident with the faunal changes among tetrapods. Future work directed toward improved absolute age assessments for major faunal assemblages will be critical for a better understanding of the transition from therapsid-dominated to dinosaur-dominated communities during the early Mesozoic.