Large igneous provinces and mass extinctions: an update

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 great catastrophe: causes of the Permo-Triassic marine mass extinction

The marine losses during the Permo-Triassic mass extinction were the worst ever experienced. All groups were badly affected, especially amongst the benthos (e.g. brachiopods, corals, bryozoans, foraminifers, ostracods). Planktonic populations underwent a fundamental change with eukaryotic algae being replaced by nitrogen-fixing bacteria, green-sulphur bacteria, sulphate-reducing bacteria and prasinophytes. Detailed studies of boundary sections, especially those in South China, have resolved the crisis to a ∼55 kyr interval straddling the Permo-Triassic boundary. Many of the losses occur at the beginning and end of this interval painting a picture of a two-phase extinction. Improved knowledge of the extinction has been supported by numerous geochemical studies that allow diverse proposed extinction mechanisms to be studied. A transition from oxygenated to anoxic-euxinic conditions is seen in most sections globally, although the intensity and timing shows regional variability. Decreased ocean ventilation coincides with rapidly rising temperatures and many extinction scenarios attribute the losses to both anoxia and high temperatures. Other kill mechanisms include ocean acidification for which there is conflicting support from geochemical proxies and, even less likely, siltation (burial under a massive influx of terrigenous sediment) which lacks substantive sedimentological evidence. The ultimate driver of the catastrophic changes at the end of the Permian was likely Siberian Trap eruptions and their associated carbon dioxide emissions with consequences such as warming, ocean stagnation and acidification. Volcanic winter episodes stemming from Siberian volcanism have also been linked to the crisis, but the short-term nature of these episodes (<decades) and the overwhelming evidence for rapid warming during the crisis makes this an unlikely cause. Finally, whilst the extinction is well studied in equatorial latitudes, a different history is found in northern Boreal latitudes including an earlier crisis which merits further study in order to fully understand the course and cause of the Permo-Triassic extinctions

Sequence stratigraphy, chemostratigraphy and facies analysis of Cambrian Series 2 – Series 3 boundary strata in northwestern Scotland

Globally, the Series 2 – Series 3 boundary of the Cambrian System coincides with a major carbon isotope excursion, sea-level changes and trilobite extinctions. Here we examine the sedimentology, sequence stratigraphy and carbon isotope record of this interval in the Cambrian strata (Durness Group) of NW Scotland. Carbonate carbon isotope data from the lower part of the Durness Group (Ghrudaidh Formation) show that the shallow-marine, Laurentian margin carbonates record two linked sea-level and carbon isotopic events. Whilst the carbon isotope excursions are not as pronounced as those expressed elsewhere, correlation with global records (Sauk I – Sauk II boundary and Olenellus biostratigraphic constraint) identifies them as representing the local expression of the ROECE and DICE. The upper part of the ROECE is recorded in the basal Ghrudaidh Formation whilst the DICE is seen around 30m above the base of this unit. Both carbon isotope excursions co-occur with surfaces interpreted to record regressive–transgressive events that produced amalgamated sequence boundaries and ravinement/flooding surfaces overlain by conglomerates of reworked intraclasts. The ROECE has been linked with redlichiid and olenellid trilobite extinctions, but in NW Scotland, Olenellus is found after the negative peak of the carbon isotope excursion but before sequence boundary formation

An abrupt extinction in the Middle Permian (Capitanian) of the Boreal Realm (Spitsbergen) and its link to anoxia and acidification

The controversial Capitanian (Middle Permian, 262 Ma) extinction event is only known from equatorial latitudes, and consequently its global extent is poorly resolved. We demonstrate that there were two, severe extinctions amongst brachiopods in northern Boreal latitudes (Spitsbergen) in the Middle to Late Permian, separated by a recovery phase. New age dating of the Spitsbergen strata (belonging to the Kapp Starostin Formation), using strontium isotopes and d13C trends and comparison with better-dated sections in Greenland, suggests that the first crisis occurred in the Capitanian. This age assignment indicates that this Middle Permian extinction is manifested at higher latitudes. Redox proxies (pyrite framboids and trace metals) show that the Boreal crisis coincided with an intensification of oxygen depletion, implicating anoxia in the extinction scenario. The widespread and near-total loss of carbonates across the Boreal Realm also suggests a role for acidification in the crisis. The recovery interval saw the appearance of new brachiopod and bivalve taxa alongside survivors, and an increased mollusk dominance, resulting in an assemblage reminiscent of younger Mesozoic assemblages. The subsequent end-Permian mass extinction terminated this Late Permian radiation

Ultra-shallow-marine anoxia in an Early Triassic shallow-marine clastic ramp (Spitsbergen) and the suppression of benthic radiation

Lower Triassic marine strata in Spitsbergen accumulated on a mid-to-high latitude ramp in which high-energy foreshore and shoreface facies passed offshore into sheet sandstones of probable hyperpycnite origin. More distal facies include siltstones, shales and dolomitic limestones. Carbon isotope chemostratigraphy comparison allows improved age dating of the Boreal sections and shows a significant hiatus in the upper Spathian. Two major deepening events, in earliest Griesbachian and late Smithian time, are separated by shallowing-upwards trends that culminated in the Dienerian and Spathian substages. The redox record, revealed by changes in bioturbation, palaeoecology, pyrite framboid content and trace metal concentrations, shows anoxic phases alternating with intervals of better ventilation. Only Dienerian–early Smithian time witnessed persistent oxygenation that was sufficient to support a diverse benthic community. The most intensely anoxic, usually euxinic, conditions are best developed in offshore settings, but at times euxinia also developed in upper offshore settings where it is even recorded in hyperpycnite and storm-origin sandstone beds: an extraordinary facet of Spitsbergen's record. The euxinic phases do not track relative water depth changes. For example, the continuous shallowing upwards from the Griesbachian to lower Dienerian was witness to several euxinic phases separated by intervals of more oxic, bioturbated sediments. It is likely that the euxinia was controlled by climatic oscillations rather than intra-basinal factors. It remains to be seen if all the anoxic phases found in Spitsbergen are seen elsewhere, although the wide spread of anoxic facies in the Smithian/Spathian boundary interval is clearly a global event

Permian (Artinskian to Wuchapingian) conodont biostratigraphy in the Tiegiao section, Laibin area, South China

Permian strata from the Tieqiao section (Jiangnan Basin, South China) contain several distinctive conodont assemblages. Early Permian (Cisuralian) assemblages are dominated by the genera Sweetognathus, Pseudosweetognathus and Hindeodus with rare Neostreptognathodus and Gullodus. Gondolellids are absent until the end of the Kungurian stage—in contrast to many parts of the world where gondolellids and Neostreptognathodus are the dominant Kungurian conodonts. A conodont changeover is seen at Tieqiao and coincided with a rise of sea level in the late Kungurian to the early Roadian: the previously dominant sweetognathids were replaced by mesogondolellids. The Middle and Late Permian (Guadalupian and Lopingian Series) witnessed dominance of gondolellids (Jinogondolella and Clarkina), the common presence of Hindeodus and decimation of Sweetognathus. Twenty main and seven subordinate conodont zones are recognised at Tieqiao, spanning the lower Artinskian to the middle Wuchiapingian Stage. The main (first appearance datum) zones are, in ascending order by stage: the Sweetognathus (Sw.) whitei, Sw. toriyamai, and Sw. asymmetrica n. sp. Zones for the Artinskian; the Neostreptognathodus prayi, Sw. guizhouensis, Sw. iranicus, Sw. adjunctus, Sw. subsymmeticus and Sw. hanzhongensis Zones for the Kungurian; the Jinogondolella (J.) nankingensis Zone for the Roadian; the J. aserrata Zone for the Wordian; the J. postserrata, J. shannoni, J. altudaensis, J. prexuanhanensis, J. xuanhanensis, J. granti and Clarkina (C.) hongshuiensis Zones for the Capitanian and the C. postbitteri Zone and C. transcaucasica Zone for the base and middle of the Wuchiapingian. The subordinate (interval) zones are the Pseudosweetognathus (Ps.) costatus, Ps. monocornus, Hindeodus (H.) gulloides, Pseudohindeodus ramovsi, Gullodus (G.) sicilianus, G. duani and H. excavates Zones. In addition, three new species, Gullodus tieqiaoensis n. sp., Pseudohindeodus elliptica n. sp. and Sweetognathus asymmetrica n. sp. are described. Age assignments for less common species (e.g., G. duani, H. catalanoi and Pseudosweetognathus monocornus etc.) are reassessed based on a rich conodont collection

Ammonium ocean following the end-Permian mass extinction

The aftermath of end-Permian mass extinction was marked by a ~5 million year interval of poorly-understood, extreme environments that likely hindered biotic recovery. Contemporary nitrogen isotope variations are considered, using a new conceptual model, to support a scenario that shows intensive nitrate-removal processes gradually depleted the global oceanic nitrate inventory during long-lasting oceanic anoxia. Enhanced nitrogen fixation shifted the oceanic nitrogenous nutrient (nutrient-N) inventory to an ammonium dominated state. Ammonium is toxic to animals and higher plants but fertilizes algae and bacteria. This change in ocean chemistry could account for the intense and unexplained losses of nektonic taxa and the proliferation of microbial blooms in the Early Triassic. The transition from a nitrate ocean to an ammonium ocean was accompanied by a decrease in respiration efficiency of organisms and a shrinking oceanic nutrient-N inventory, ultimately leading to generally low productivity in the Early Triassic oceans. These unappreciated nutrient changes during episodes of prolonged ocean anoxia may be the key life-limiting factor at such times