Abstract In Late Triassic (Norian–Rhaetian) times, the Jameson Land Basin lay at 40° N on the northern part of the supercontinent Pangaea. This position placed the basin in a transition zone between the relatively dry interior of the supercontinent and its more humid periphery. Sedimentation in the Jameson Land Basin took place in a lake–mudflat system and was controlled by orbitally forced variations in precipitation. Vertebrate fossils have consistently been found in these lake deposits (Fleming Fjord Formation), and include fishes, dinosaurs, amphibians, turtles, aetosaurs and pterosaurs. Furthermore, the fauna includes mammaliaform teeth and skeletal material. New vertebrate fossils were found during a joint vertebrate palaeontological and sedimentological expedition to Jameson Land in 2012. These new finds include phytosaurs, a second stem testudinatan specimen and new material of sauropodomorph dinosaurs, including osteologically immature individuals. Phytosaurs are a group of predators common in the Late Triassic, but previously unreported from Greenland. The finding includes well-preserved partial skeletons that show the occurrence of four individuals of three size classes. The new finds support a late Norian–early Rhaetian age for the Fleming Fjord Formation, and add new information on the palaeogeographical and palaeolatitudinal distribution of Late Triassic faunal provinces.

The temporal link between mass extinctions and large igneous provinces is well known. Here, we examine this link by focusing on the potential climatic effects of large igneous province eruptions during several extinction crises that show the best correlation with mass volcanism: the Frasnian-Famennian (Late Devonian), Capitanian (Middle Permian), end-Permian, end-Triassic, and Toarcian (Early Jurassic) extinctions. It is clear that there is no direct correlation between total volume of lava and extinction magnitude because there is always sufficient recovery time between individual eruptions to negate any cumulative effect of successive flood basalt eruptions. Instead, the environmental and climatic damage must be attributed to single-pulse gas effusions. It is notable that the best-constrained examples of death-by-volcanism record the main extinction pulse at the onset of (often explosive) volcanism (e.g., the Capitanian, end-Permian, and end-Triassic examples), suggesting that the rapid injection of vast quantities of volcanic gas (CO 2 and SO 2 ) is the trigger for a truly major biotic catastrophe. Warming and marine anoxia feature in many extinction scenarios, indicating that the ability of a large igneous province to induce these proximal killers (from CO 2 emissions and thermogenic greenhouse gases) is the single most important factor governing its lethality. Intriguingly, many voluminous large igneous province eruptions, especially those of the Cretaceous oceanic plateaus, are not associated with significant extinction losses. This suggests that the link between the two phenomena may be controlled by a range of factors, including continental configuration, the latitude, volume, rate, and duration of eruption, its style and setting (continental vs. oceanic), the preexisting climate state, and the resilience of the extant biota to change.

The Hirnantian mass extinction is recognized as the first of the “big three” extinctions and, along with the end-Permian and end-Cretaceous events, is the result of an acceleration in biotic extinctions concomitant with a rise in originations. The Hirnantian mass extinction is characterized by high taxonomic impact and within-community extinctions. The Hirnantian mass extinction is also unusual in that (1) it is associated with glaciation, but there is little evidence elsewhere in the younger Phanerozoic that glaciations have been a cause of mass extinction, and (2) there is limited understanding of how glaciation could directly cause mass extinction, particularly in the marine realm. In this review, we argue that coordinated extinctions occurred at the onset and termination of glaciation and were due to climatically induced changes in relative sea level, ocean redox stratification, and sea-surface temperature gradients. These earth system changes resulted in a reduction in prospective niche space, both in the water column and on the seafloor, which in turn led to increased competition and selection pressures, resulting in extinctions where the carrying capacities of particular ecological niches were exceeded. The long-term ventilation of the oceans broke the link between glaciation and mass extinction.

The Ordovician Period (ca. 488–444 Ma) witnessed profound changes in the biodiversity and biocomplexity of marine life, marked by the installation of a benthos dominated by suspension-feeding animals, most notably the brachiopods. The Ordovician brachiopod fauna was dominated by rhynchonelliformeans in contrast to that of the underlying Cambrian System, characterized by a diversity of various non-articulated groups. Over an interval of some 25 m.y., accelerating γ (inter-provincial), β (inter-community), and α (intra-community) diversity was initiated by high diversities among Early Ordovician brachiopod faunas associated with the dispersal of the continents and the high frequency of volcanic arcs and microcontinents (γ diversity). During the Early and Middle Ordovician, community types expanded particularly into deeper water and around carbonate platforms and structures (β diversity). Moreover, during the period the α diversity of individual assemblages increased from <10 species during the Late Cambrian to ~30 in the Late Ordovician, with the canalization of ecological niches and the opportunity for more densely packed communities. The end-Ordovician extinction event was a severe crisis for the more common Ordovician taxa, the orthide and strophomenide brachiopods. Whereas some widespread taxa, characteristic of deep-water environments, survived, many from shallower-water, together with those from the deep shelf and slope, disappeared. The subsequent Silurian fauna became increasingly dominated by atrypide, athyridide, spiriferide, and rhynchonellide brachiopods.

Newly recognized cyclomedusoid fossils in the Antelope Mountain Quartzite confirm that it is latest Neoproterozoic (Ediacaran) in age. Biogeographic affinities of the cyclomedusoid fossils suggest that the Yreka subterrane and its close associate, the Trinity subterrane, formed after the breakup of Rodinia in an ocean basin bordering Australia, northern Canada, Siberia, and Baltica. Reevaluating biogeographic, geological, and paleomagnetic evidence in the context of this starting point, the Yreka subterrane and Trinity subterrane may have been located at either 7°N or 7°S latitude ca. 580–570 Ma, but were not necessarily close to Laurentia. Continental detrital zircons (3.2–1.3 Ga) in the Antelope Mountain Quartzite most likely came from Australia or Siberia rather than Laurentia. The Yreka subterrane and Trinity subterrane record ∼180 m.y. of active margin events somewhere in Panthalassa (Proto-Pacific Ocean). Paleozoic biogeographic data, paleomagnetism, and regional relationships indicate that Yreka subterrane and Trinity subterrane were located throughout the early Paleozoic in the part of Panthalassa surrounded by Australia, NW Laurentia, Siberia, China, Baltica, and the Uralian terranes. By the mid-Devonian they were located at 31°N or 31°S in a somewhat isolated location, probably in a Northern Hemisphere oceanic plateau or island chain well outboard of other tectonic elements, and by the Permian they were almost completely isolated from other tectonic elements. The Yreka subterrane, as part of the Klamath superterrane, was not native to North America and did not accrete to it until the Early Cretaceous.

Three brachiopod faunas discussed herein record different depositional and tectonic settings along the southwestern margin of Laurentia (North America) during Devonian time. Depositional settings include inner continental shelf (Cerros de Los Murciélagos), medial continental shelf (Rancho Placeritos), and offshelf continental rise (Rancho Los Chinos). Ages of Devonian brachiopod faunas include middle Early (Pragian) at Rancho Placeritos in west-central Sonora, late Middle (Givetian) at Cerros de Los Murciélagos in northwestern Sonora, and late Late (Famennian) at Rancho Los Chinos in central Sonora. The brachiopods of these three faunas, as well as the gastropod Orecopia , are easily recognized in outcrop and thus are useful for local and regional correlations. Pragian brachiopods dominated by Acrospirifer and Meristella in the “San Miguel Formation” at Rancho Placeritos represent the widespread Appohimchi Subprovince of eastern and southern Laurentia. Conodonts of the early to middle Pragian sulcatus to kindlei Zones associated with the brachiopods confirm the ages indicated by the brachiopod fauna and provide additional information on the depositional setting of the Devonian strata. Biostratigraphic distribution of the Appohimchi brachiopod fauna indicates continuous Early Devonian shelf deposition along the entire southern margin of Laurentia. The largely emergent southwest-trending Transcontinental arch apparently formed a barrier preventing migration and mixing of many genera and species of brachiopods from the southern shelf of Laurentia in northern Mexico to the western shelf (Cordilleran miogeocline) in the western United States. Middle Devonian Stringocephalus brachiopods and Late Devonian Orecopia gastropods in the “Los Murciélagos Formation” in northwest Sonora represent the southwesternmost occurrence of these genera in North America and date the host rocks as Givetian and Frasnian, respectively. Rhynchonelloid brachiopods ( Dzieduszyckia sonora ) and associated worm tubes in the Los Pozos Formation of the Sonora allochthon in central Sonora are also found in strati-form-barite facies in the upper Upper Devonian (Famennian) part of the Slaven Chert in the Roberts Mountains allochthon (upper plate) of central and western Nevada. Although these brachiopods and worm tubes occur in similar depositional settings along the margin of Laurentia in Mexico, they occur in allochthons that exhibit different tectonic styles and times of emplacement. Thus, the allochthons containing the brachiopods and worm tubes in Sonora and Nevada are parts of separate orogenic belts and have different geographic settings and tectonic histories. Devonian facies belts and faunas in northern Mexico indicate a continuous continental shelf along the entire southern margin of Laurentia. These data, in addition to the continuity of the late Paleozoic Ouachita-Marathon-Sonora orogen across northern Mexico, contradict the early Late Jurassic Mojave-Sonora megashear as a viable hypothesis for large-magnitude offset (600–1100 km) of Proterozoic through Middle Jurassic rocks from California to Sonora.