Spatial variation in sediment fluxes, redox conditions, and productivity in the Permian–Triassic Panthalassic Ocean

241

193

Delayed Earth system recovery following the end-Permian mass extinction is often attributed to severe ocean anoxia. However, the extent and duration of Early Triassic anoxia remains poorly constrained. Here we use paired records of uranium concentrations ([U]) and 238 U/ 235 U isotopic compositions (δ 238 U) of Upper Permian−Upper Triassic marine limestones from China and Turkey to quantify variations in global seafloor redox conditions. We observe abrupt decreases in [U] and δ 238 U across the end-Permian extinction horizon, from ∼3 ppm and −0.15‰ to ∼0.3 ppm and −0.77‰, followed by a gradual return to preextinction values over the subsequent 5 million years. These trends imply a factor of 100 increase in the extent of seafloor anoxia and suggest the presence of a shallow oxygen minimum zone (OMZ) that inhibited the recovery of benthic animal diversity and marine ecosystem function. We hypothesize that in the Early Triassic oceans-characterized by prolonged shallow anoxia that may have impinged onto continental shelvesglobal biogeochemical cycles and marine ecosystem structure became more sensitive to variation in the position of the OMZ. Under this hypothesis, the Middle Triassic decline in bottom water anoxia, stabilization of biogeochemical cycles, and diversification of marine animals together reflect the development of a deeper and less extensive OMZ, which regulated Earth system recovery following the end-Permian catastrophe.paleoredox | uranium isotopes | biogeochemical cycling | carbon isotopes | Early TriassicT he end-Permian mass extinction-the most severe biotic crisis in the history of animal life-was followed by 5 million years of reduced biodiversity (1, 2), limited ecosystem complexity (3), and large perturbations in global biogeochemical cycling (4, 5). Ocean anoxia has long been invoked both as a cause of the extinction (6-8) and as a barrier to rediversification (9). Numerous lines of evidence demonstrate widespread anoxic conditions around the time of the end-Permian mass extinction (e.g., refs. 6 and 10-12). In contrast, the prevalence of anoxia during the 5-to 10-millionyear recovery interval remains poorly constrained (13,14).Reconstructing paleoredox conditions is challenging because some indicators of anoxia characterize only the local conditions of the overlying water column, whereas other indicators may be influenced by confounding factors, such as weathering rates on land. Here, we use paired measurements of [U] and δ 238 U in marine carbonate rocks to differentiate changes in weathering of U from variations in global marine redox conditions. Microbially mediated reduction of U(VI) to U(IV) under anoxic conditions at the sediment−water interface results in a substantial decrease in uranium solubility and a measureable change in 238 U/ 235 U (15-18). Because 238 U is preferentially reduced and immobilized relative to 235 U, the δ 238 U value of seawater U(VI) decreases as the areal extent of bottom water anoxia increases (Fig. S1). Consequently, a global increase in the extent of anoxi...

Section: Discussionmentioning

confidence: 85%

Marine anoxia and delayed Earth system recovery after the end-Permian extinction

Lau

Maher

Altıner

et al. 2016

241

193

“…In addition, a marine region would be targeted that is the locus of Paleozoic biological activity (the neritic realm), and thereby this conceptual model fulfills all criteria as suggested by Wignall and Twitchett (5) to explain a wholesale collapse of marine invertebrate diversity. However, the geography and nutrient load of weathering fluxes would also be an important determinant of the spatial distribution and severity of productivity-driven redox changes (oxic, nonsulfidic anoxic, and euxinic) (41). Regionally biased ecosystem destruction would leave refugia with less adverse conditions and would allow rapid recolonization of vacant ecospaces through migration of survivors.…”

Section: Resultsmentioning

confidence: 99%

Flourishing ocean drives the end-Permian marine mass extinction

Schobben

Stebbins

Ghaderi

et al. 2015

The end-Permian mass extinction, the most severe biotic crisis in the Phanerozoic, was accompanied by climate change and expansion of oceanic anoxic zones. The partitioning of sulfur among different exogenic reservoirs by biological and physical processes was of importance for this biodiversity crisis, but the exact role of bioessential sulfur in the mass extinction is still unclear. Here we show that globally increased production of organic matter affected the seawater sulfate sulfur and oxygen isotope signature that has been recorded in carbonate rock spanning the Permian−Triassic boundary. A bifurcating temporal trend is observed for the strata spanning the marine mass extinction with carbonate-associated sulfate sulfur and oxygen isotope excursions toward decreased and increased values, respectively. By coupling these results to a box model, we show that increased marine productivity and successive enhanced microbial sulfate reduction is the most likely scenario to explain these temporal trends. The new data demonstrate that worldwide expansion of euxinic and anoxic zones are symptoms of increased biological carbon recycling in the marine realm initiated by global warming. The spatial distribution of sulfidic water column conditions in shallow seafloor environments is dictated by the severity and geographic patterns of nutrient fluxes and serves as an adequate model to explain the scale of the marine biodiversity crisis. Our results provide evidence that the major biodiversity crises in Earth's history do not necessarily implicate an ocean stripped of (most) life but rather the demise of certain eukaryotic organisms, leading to a decline in species richness.sulfur cycle | end-Permian mass extinction | primary productivity

“…Indeed, there is evidence for sulfidic AMZs in the North Atlantic during the Cretaceous ocean anoxic event 2 at the Cenomanian/ Turonian boundary (65), at the Permian/ Triassic boundary (66), and for time periods in the Precambrian (67). Because modern AMZs support the same biogeochemical cycles as sulfidic water bodies today, and presumably also sulfidic AMZs of the past, one can view them as a particular chemical intermediate state between two "end points" represented by fully oxic systems and fully sulfidic systems (Fig.…”

Section: How Are Microbial Communities and Biogeochemical Processes Cmentioning

confidence: 99%

Microbial oceanography of anoxic oxygen minimum zones

Ulloa

Canfield

DeLong

et al. 2012

394

403

Vast expanses of oxygen-deficient and nitrite-rich water define the major oxygen minimum zones (OMZs) of the global ocean. They support diverse microbial communities that influence the nitrogen economy of the oceans, contributing to major losses of fixed nitrogen as dinitrogen (N 2 ) and nitrous oxide (N 2 O) gases. Anaerobic microbial processes, including the two pathways of N 2 production, denitrification and anaerobic ammonium oxidation, are oxygen-sensitive, with some occurring only under strictly anoxic conditions. The detection limit of the usual method (Winkler titrations) for measuring dissolved oxygen in seawater, however, is much too high to distinguish low oxygen conditions from true anoxia. However, new analytical technologies are revealing vanishingly low oxygen concentrations in nitriterich OMZs, indicating that these OMZs are essentially anoxic marine zones (AMZs). Autonomous monitoring platforms also reveal previously unrecognized episodic intrusions of oxygen into the AMZ core, which could periodically support aerobic metabolisms in a typically anoxic environment. Although nitrogen cycling is considered to dominate the microbial ecology and biogeochemistry of AMZs, recent environmental genomics and geochemical studies show the presence of other relevant processes, particularly those associated with the sulfur and carbon cycles. AMZs correspond to an intermediate state between two "end points" represented by fully oxic systems and fully sulfidic systems. Modern and ancient AMZs and sulfidic basins are chemically and functionally related. Global change is affecting the magnitude of biogeochemical fluxes and ocean chemical inventories, leading to shifts in AMZ chemistry and biology that are likely to continue well into the future.