Kaolinite from the Black Ridge, Clermont, has relatively low δ18O (12.3‰ to 14.8‰) and very low δD values with a large variation (−120‰ to −85‰). Comparison of these data with those from the nearby Denison Trough and elsewhere in eastern Australia, together with previous studies of the mineralogy of the sedimentary rocks, suggests that extensive kaolinization of the “White Section” resulted from weathering during the Late Triassic to Early Jurassic periods. The relatively large variation in δD values of kaolinite probably derives from post-formational isotopic exchange with other fluids.

The similarity between δ18O values of kaolinites from Black Ridge and from the Denison Trough suggests that the small Miclere-Black Ridge basin may have been part of the Denison Trough before the Late-Triassic inversion. The preservation of original δD values in kaolinite at Black Ridge indicates that unlike the Denison Trough, which was reburied at more than 1000 m, the Miclere-Black Ridge basin was not rebuffed at great depth during the Mesozoic period.

Chondrichthyan and actinopterygian fish remains from Rhaetian (c. 208.05–201.36 Ma) or perhaps Late Norian deposits in the Winterswijk quarry are described. The most abundant taxon is the actinopterygian Gyrolepis albertii, followed by the chondrichthyan Lissodus minimus. Furthermore, the palaeopterygian actinopterygians Saurichthys longidens and Birgeria acuminata, and some teeth of neopterygians Sargodon tomicus, ‘Lepidotes’ sp. and indeterminate pycnodontiforms are recorded in addition to the chondrichthyans Rhomphaiodon minor, Parascylloides turnerae and some ‘Hybodus’ cf. cuspidatus (senior synonym of H. cloacinus). Chondrichthyan dermal denticles, actinopterygian scales and gill rakers, tooth plates, and some fish bones were also found. There is considerable faunal resemblance to the various localities from the Rhaetian of the British Penarth Group, although it depends on the location as to whether chondrichthyans or actinopterygians prevail in the samples. On average, there are more chondrichthyan teeth present in the British samples than actinopterygian teeth, which is opposite to the situation in Winterswijk. That might be explained by different ecological circumstances, such as lower oxygen levels in bottom waters in Winterswijk and freshwater input and/or changes in salinity in the UK.

The relationship between magmatism and gold mineralization has been a topic of interest in understanding the formation of ore deposits. The Baizhangzi gold deposit, located in the northern margin of the North China Craton, is hosted by the Baizhangzi granite (BZG) and provides a case to evaluate the relation between granite and gold mineralization in Late Triassic. In this study, we present petrography, bulk geochemistry, zircon U-Pb isotope and trace elements data, as well as major elements of biotite and plagioclase for the BZG to evaluate the petrogenesis and link with gold mineralization. The BZG comprises biotite monzogranite, biotite-bearing monzogranite and monzogranite (BZGs). Zircon U-Pb geochronology shows that all the granitoids of BZGs were coeval with a formation age of 232 Ma. The granitoids, with high SiO2, Al2O3 and Sr, while low Y and Yb, show adakitic affinity. They are enriched in LILFs (e.g., Rb, Ba, Th, U and Sr) and LREEs, while depletion in HFSEs (e.g., Nb, Ta, P and Ti). The geochemical and mineral chemical data suggest that the granitoids have experienced the fractional crystallization of biotite + plagioclase + K- feldspar + apatite. Crystallization temperature is estimated as ca. 700°C, and pressure is between 0.71 kbar and 1.60 kbar. The monzogranite shows higher values of logfO2, △FMQ and △NNO than the biotite-bearing monzogranite, ranging from −19.76 to −11.71, −4.93 to +3.67 and −5.48 to +3.11, respectively. The fractional crystallization, together with high fO2, K-metasomatism and low evolution degree, provided favourable conditions for gold mineralization.

Subdivisions of Ladinian–Carnian boundary beds and the lower Carnian strata in South China are challenging owing to a paucity of west Tethyan ammonoids. We investigated a conodont fauna in a continuous section at Yize in eastern Yunnan Province to provide a biostratigraphic solution. Five genera and 24 conodont species are recognized, and five conodont zones are established. The zones are, in ascending order, the Paragondolella inclinata Zone, the Quadralella polygnathiformis Zone, the Quadralella praelindae Zone, the Quadralella auriformis Zone and the Quadralella robusta Zone. The Ladinian–Carnian boundary is provisionally defined by the first occurrences of Quadralella polygnathiformis and Quadralella intermedia in the cherty limestone member of the Zhuganpo Formation. Regional correlations via conodont biostratigraphy indicate that the Zhuganpo Formation is probably diachronous, with a maximal range spanning the upper Ladinian to the lower Carnian. Amongst all common late Ladinian – early Carnian conodont genera, Paragondolella, Quadralella and Mazzaella are probably cosmopolitan. Budurovignathus was restricted to a few basins and probably preferred offshore or deep-water environments.

The first ichthyosaurian specimens discovered from the Upper Triassic of the Russian Arctic (Kotelny Island, New Siberian Islands) are described herein. They include the remains of large- to small-bodied ichthyosaurians originating from six stratigraphic levels spanning the lower Carnian to middle Norian. The material is mostly represented by isolated vertebrae and ribs, which are not possible to accurately diagnose, but also includes specimens comprising associated vertebrae and a fragmentary skeleton that preserves cranial remains (parabasisphenoid, fragmentary quadrate, partial mandible and hyoids). Based on vertebral and rib morphology, we identify the specimens as representatives of the following taxonomic groups: large-bodied shastasaurids, medium-sized indeterminate ichthyosaurians with a single rib facet in the presacral centra, and small euichthyosaurians with double rib facets present throughout the presacral vertebrae that likely represent toretocnemids and/or basal parvipelvians. In addition, the cranial and mandibular remains preserved in one of the specimens, ZIN PH 5/250, were studied using micro-computed tomography. Its mandible is highly similar to that of toretocnemids, whereas the parabasisphenoid demonstrates a peculiar combination of both plesiomorphic and derived character states, providing the first detailed data on this cranial element in a Late Triassic ichthyosaurian. Furthermore, the specimen also demonstrates a distinctive condition of rib articulation in the anteriormost presacral (cervical) vertebrae, which together with other features allows for the erection of a new taxon – Auroroborealia incognita gen. et sp. nov. Although the phylogenetic position of this taxon is uncertain due to its fragmentary nature, its anatomy, indicating toretocnemid or parvipelvian affinities, further supports the previously hypothesised sister-group relationships between these two clades. The morphology of the parabasisphenoid and vertebral column of the new taxon is discussed in broader contexts of the patterns of evolution of these skeletal regions in ichthyosaurs.

The Triassic–Jurassic Upper Karoo Group of the Mid-Zambezi Basin (MZB; Zimbabwe) includes a thick succession of terrestrial sediments with high palaeontological potential that has been neglected since the 1970s. Here, we review the Upper Karoo Group stratigraphy, present detailed sedimentological work and identify new vertebrate-bearing sites at several measured sections along the southern shore of Lake Kariba. These fossil-bearing sites fall within the Pebbly Arkose and Forest Sandstone formations, and are the first to be recorded from the region since the discovery of Vulcanodon karibaensis nearly 50 years ago. The unique and diverse assemblage of aquatic and terrestrial fauna reported includes phytosaurs, metoposaurid amphibians, lungfish, non-dinosaurian archosauromorphs and non-sauropod sauropodomorph dinosaurs. This improvement of Upper Karoo Group biostratigraphy is important in refining its temporal resolution, and impacts both regional and global studies. Finally, the new fossil sites demonstrate the palaeontological importance of the MZB and its role in providing a holistic understanding of early Mesozoic ecosystems in southern Gondwana.

The pseudosuchian archosaur Ornithosuchus, from the Lossiemouth Sandstone Formation (Late Triassic), Scotland, was the first ornithosuchid to be discovered, and the only one recorded, in the northern hemisphere. The fossil record of “Ornithosuchus longidens” is mainly based on natural moulds and, in a few cases, three-dimensional bony elements, complicating the interpretation of its anatomy. The taxonomy of this species has changed several times since the late 1800s and here we revisit its current status. The synonymy of “Dasygnathoides longidens” and Ornithosuchus woodwardi proposed by Walker (1964) is rejected, based on new interpretations of the holotype and referred specimens of “Dasygnathoides longidens”. The latter species is considered as a nomen dubium, because it lacks diagnostic features and cannot be identified beyond Pseudosuchia. As a result, Ornithosuchus woodwardi is resurrected as a valid species and its diagnosis is emended. The body size range of Ornithosuchus woodwardi is reduced to about a half, because ELGNM 1, previously considered the largest specimen of the genus, can no longer be referred to it. “Dasygnathoides longidens” cannot be assigned to any of the known archosauriforms from the Lossiemouth Sandstone Formation, but it still represents the largest predator currently known for its fauna.

Historic type and referred material of the aetosaurian taxa Typothorax coccinarum, Episcoposaurus horridus and Episcoposaurus haplocerus are redescribed and the non-aetosaurian material identified and removed, a task previously considered “hopeless”. Reexamination of the original material reveals that the holotypes of E. haplocerus and probably T. coccinarum are not diagnosable at the species level and therefore are nomena dubia. The next available names for material referred to these taxa are Desmatosuchus spurensis and E. horridus respectively, although it may be more desirable for reasons of taxonomic stability to attempt to petition for a neotype in the latter case. The redescription of historical specimens is necessary to determine their nomenclatural validity. The use of referred specimens as proxy “type” specimens is problematic, as these referrals were originally made not on the basis of apomorphies, but rather on biostratigraphic and/or geographical assumptions which are inherently circular and cannot be unambiguously supported.

The problem of the origin of dinosaurs has historically had three dimensions. The first is the question of whether Dinosauria is monophyletic, and of its relationships to other archosaurs. This question was plagued from the beginning by a lack of relevant fossils, an historical burden of confusing taxonomic terms and a rudimentary approach to devising phylogenies. The second dimension concerns the functional and ecological adaptations that differentiated dinosaurs from other archosaurs, a question also marred by lack of phylogenetic clarity and testable biomechanical hypotheses. The third dimension comprises the stratigraphic timing of the origin of dinosaurian groups with respect to each other and to related groups, the question of its synchronicity among various geographic regions, and some of the associated paleoenvironmental circumstances. None of these dimensions alone answers the question of dinosaur origins, and they sometimes provide conflicting implications. Since Dinosauria was named, one or another set of questions has historically dominated academic discussion and research. Paradigms have shifted substantially in recent decades, and current evidence suggests that we are due for more such shifts. I suggest two changes in thinking about the beginning of the “Age of Dinosaurs”: first, the event that we call the (phylogenetic) origin of dinosaurs was trivial compared to the origin of Ornithodira; and second, the “Age of Dinosaurs” proper did not begin until the Jurassic. Re-framing our thinking on these issues will improve our understanding of clade dynamics, timing of macroevolutionary events, and the effects of Triassic climate change on terrestrial vertebrates.

The Newark-APTS established a high-resolution framework for the Late Triassic and Early Jurassic. Palaeomagnetic polarity correlations to marine sections show that stage-level correlations of continental sequences were off by as much as 10 million years. New U–Pb ages show the new correlations and the Newark basin astrochronology to be accurate. Correlation of Newark-APTS to the Chinle Formation/Dockum Group, Glen Canyon Group, Fleming Fjord Formation and Ischigualasto Formation led to the following conclusions: (1) there are no unequivocal Carnian-age dinosaurs; (2) the Norian Age was characterised by a slowly increasing saurischian diversity but no unequivocal ornithischians; (3) there was profound Norian and Rhaetian continental provinciality; (4) the classic Chinle-, Germanic- and Los Colorados-type assemblages may have persisted to the close of the Rhaetian; (5) the distinct genus-level biotic transition traditionally correlated with the marine Carnian–Norian is in fact mid-Norian in age and within published error of the Manicouagan impact; (6) the end-Triassic marine and continental extinctions as seen in eastern North America were contemporaneous; and (7) compared to Triassic communities, Hettangian and Sinemurian age terrestrial communities were nearly globally homogenous and of low diversity. Consequently, the complex emerging picture of dinosaur diversification demands biostratigraphically-independent geochronologies in each of the faunally-important regions.

Many hypotheses have been proposed for the rise of dinosaurs, but their early diversification remains poorly understood. This paper examines the occurrences, species diversity and abundance of early dinosaurs at both regional and global scales to determine patterns of their early evolutionary history. Four main patterns are clear: (1) sauropodomorph dinosaurs became abundant during the late Norian–Rhaetian of Gondwana and Europe; (2) Triassic dinosaurs of North America have low species diversity and abundance until the beginning of the Jurassic; (3) sauropodomorphs and ornithischians are absent in the Triassic of North America; and (4) ornithischian dinosaurs maintain low species diversity, relative abundance and small body size until the Early Jurassic. No one hypothesis fully explains these data. There is no evidence for a Carnian–Norian extinction event, but sauropodomorphs did become abundant during the Norian in some assemblages. No clear connection exists between palaeoenvironment and early dinosaur diversity, but environmental stress at the Triassic–Jurassic boundary is consistent with changes in North American dinosaur assemblages. Elevated growth rates in dinosaurs are consistent with the gradual phyletic increase in body size. This study demonstrates that early dinosaur diversification was a complex process that was geographically diachronous and probably had several causes.

Herbivorous and omnivorous dinosaurs were rare during the Carnian stage of the Late Triassic. By contrast, the succeeding Norian stage witnessed the rapid diversification of sauropodomorphs and the rise of the clade to ecological dominance. Ornithischians, by contrast, remained relatively rare components of dinosaur assemblages until much later in the Mesozoic. The causes underlying the differential success of ornithischians and sauropodomorphs remain unclear, but might be related to trophic specialisation. Sauropodomorphs replaced an established herbivore guild consisting of rhynchosaurs, aetosaurs and basal synapsids, but this faunal turnover appears to have been opportunistic and cannot be easily attributed to either competitive interactions or responses to floral change. Consideration of diversity patterns and relative abundance suggests that the ability to eat plants might have been a major factor promoting sauropodomorph success, but that it was less important in the early evolution of Ornithischia. On the basis of current evidence it is difficult to determine the diet of the ancestral dinosaur and scenarios in which omnivory or carnivory represent the basal condition appear equally likely.

A moderately diverse assemblage of plant microfossils has been recovered from the Johnsons Dock Member of the Miers Bluff Formation, Livingston Island, including spores, pollen, acritarchs, wood fragments and cuticles. Containing a total of c. 45 of miospore taxa, the palynoflora is dominated by non-striate bisaccate pollen, but spores of pteridophytes and pollen of gymnosperms are proportionate in diversity. The palynoflora is similar in composition to those indicative of subzones C + D of the Alisporites Zone of Antarctica, and the upper Craterisporites rotundus Zone and the lower Polycingulatisporites crenulatus Zone of Australia as well as the upper Polycingulatisporites crenulatus Zone and Foveosporites moretonensis Zone of New Zealand, suggesting a Late Triassic (possibly Norian–Rhaetian) age. This determination is supported by the sporadic occurrence of Aratrisporites and Classopollis in the palynoflora as well as by the absence of striate bisaccate grains.