A remarkable specimen of the actinopterygian fish Pachycormus macropterus from the Early Jurassic (Toarcian) Posidonienschiefer Formation of Germany exceptionally preserves an unusually large ammonite inside its gut. The ammonite was swallowed by the fish, likely by accident, and represents the first direct evidence for an actinopterygian fish consuming an ammonoid. Exceptional aragonite preservation of the conch retaining partial nacreous lustre, combined with only minor acid etching of the shell, strongly indicates that the ammonite was ingested immediately prior to and was directly responsible for the fish’s death. The fish’s stomach provided a microenvironment protecting the aragonite from chemical dissolution.

This study focuses on the Tianshifu Basin, eastern Liaoning, China, which is filled with Lower–Middle Jurassic fluviolacustrine sediments rich in macroplants. Our aim is to explore the continental climate features of the late Early Jurassic period. The composition of the Early–Middle Jurassic flora and the carbon isotopic ratios of organic matter, total organic carbon, total organic nitrogen and sulphur of the rock samples from the Changliangzi section (the upper part of the Lower Jurassic deposits) have been investigated. Based on the flora, eastern Liaoning was generally characterized by temperate and humid conditions during the Early–Middle Jurassic period, but with rising temperatures during late Early Jurassic time. The sediments of the Changliangzi section show a transformation from shallow-lake facies to deep-lake facies. A positive organic carbon isotope excursion correlates with the deepening of this palaeolake, considered to be caused by climate warming. The late Early Jurassic climate warming indicated by floral and isotopic evidence corresponds to the climatic events recorded elsewhere in marine and continental sequences during the Toarcian Age, the so-called Toarcian Anoxic event, and may be associated with enhanced global greenhouse warming. This study provides new continental data supporting global warming during the late Early Jurassic period.

The Zhangguangcai Range in the Xing’an Mongolian Orogenic Belt, NE China, contains Early Jurassic (c. 188 Ma) Dabaizigou (DBZG) porphyritic dolerite. Compared with other island-arc mafic rocks, the DBZG dolerite is characterized by high trace-element contents, relatively weak Nb and Ta enrichments, and no Zr, Hf or Ti depletions, similar to OIB-type rocks. Analysed rocks have (87Sr/86Sr)i ratios of 0.7033–0.7044, relatively uniform positive ɛNd(t) values of 2.3–3.2 and positive ɛHf(t) values of 8.5–17.1. Trace-element and isotopic modelling indicates that the DBZG mafic rocks were generated by partial melting of asthenospheric mantle under garnet- to spinel-facies conditions. The occurrence of OIB-like mafic intrusion suggests significant upwelling of the asthenosphere in response to lithospheric attenuation caused by continental rifting. These processes occurred in an incipient continental back-arc environment in the upper plate of a palaeo-Pacific slab subducting W–NW beneath East Asia.

Cretaceous–Miocene adakitic rocks in the southern Lhasa sub-terrane have been intensively investigated, while possible Early Jurassic adakitic rocks in this area have been largely neglected. Petrological and geochemical studies revealed adakitic affinities of an Early Jurassic quartz diorite intrusion with mafic enclaves and three tonalite bodies from the Jiacha area in the southern Lhasa sub-terrane. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) zircon U–Pb dating suggests crystallization ages of 199–179 Ma for these rocks. Both quartz diorites and tonalites have typical adakitic geochemical characteristics such as high Al2O3 (15.14–18.22 wt.%) and Sr (363–530 ppm) contents, low Y (4.46–15.9 ppm) and Yb (0.51–1.74 ppm) contents and high Sr/Y ratios of 27–106. The adakitic quartz diorites are further characterized by high MgO (2.63–3.46 wt.%), Mg# (48–54) and εHf(t) (6.6–13.4) values, which were probably produced by partial melting of a subducted oceanic slab with a mantle contribution. The adakitic tonalites have very low abundances of compatible elements and relatively low εHf(t) values (3.5–10.3), and are interpreted to have formed by partial melting of Neoproterozoic mafic lower crust. Upwelling asthenosphere, triggered by rollback of the subducting Bangong–Nujiang (Meso-Tethys) oceanic plate, provided the necessary heat for slab and lower crust melting, resulting in the geochemical diversity of the coexisting felsic intrusive rocks. Contrary to other models, this study further demonstrates that the Bangong–Nujiang oceanic plate was subducted southward beneath the Lhasa terrane during the Early Jurassic.

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.

Comparing the Early Jurassic ammonoids found in three Italian Apennine sections (Bosso, Pallareto and Furlo) with those reported in the literature for some South American sections (Argentina and Chile), we noted that these two areas share the same late Sinemurian–early Pliensbachian faunal succession: Paltechioceras in the late Sinemurian (Raricostatum Zone), Catriceras in the earliest Pliensbachian (Jamesoni Zone, Taylori Subzone), Miltoceras in the middle part of the early Pliensbachian (Jamesoni Zone, Polymorphus Subzone). An overall similarity to Apennine and South American ammonite faunas of the same age can be found for some sections of Morocco and partially also for southern Spain. One of the Italian taxa (an unpublished early Pliensbachian Apennine genus, ascribable to the family Polymorphitidae) is reported in the South American Pacific coast by the middle to late part of the early Pliensbachian (Ibex Zone). Evolving towards more and more discoidal morphologies, it might have given rise to an endemic American ammonite group, which is represented by the genera Eoamaltheus Hillebrandt and Fanninoceras McLearn. This phylogenetic reconstruction is based on several lines of evidence (shell morphology, ontogenetic development, aspect of the suture lines, biostratigraphy), and can be safely traced back to the basal Pliensbachian strata of the Tethyan Palaeoprovince. As far as we know, the examined ammonoid taxa are exclusively found in the western Tethys (e.g. Italian Apennines) and American Pacific coast (e.g. Argentina), but they have never been recorded elsewhere, and they show no evidence of pantropical distribution. Our biostratigraphic and phylogenetic data suggest the existence of a late Sinemurian–early Pliensbachian marine connection between the western Tethys (Italian Apennines) and the South American Pacific coast (Argentina). This is the so-called Hispanic Corridor, the existence of which has already been supported by many authors using several geological and palaeontological pieces of evidence. According to our interpretation, as well as the conclusions of other workers, it was a temporary and intermittent seaway, which allowed a partial faunal exchange for some taxa (including certain shallow-water ammonoids) during Sinemurian and Pliensbachian times. This palaeobiogeographic model consistently relates the biostratigraphy and evolution of some western Tethys and South American ammonoids to the major palaeogeographic changes affecting this vast area. In any case, our working hypothesis does not have any claim of universal applicability; we deem the proto-Atlantic seaway model to be the most suitable (until proof of the contrary) for the ammonites we examined, but it may not be necessarily valid for all the currently known taxa.