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1. Changing inputs of continental and submarine weathering sources of Sr to the oceans during OAE 2

   https://doi.org/10.46427/gold2020.1889  

   Nana Yobo, L. ; Brandon, A.D. ; Holmden, C. ; Lau, K.V. ; Eldrett, J. ( June 2021 , Geochimica et cosmochimica acta)

   Jacobson, A. (Ed.)

   Ocean anoxic events (OAE) are characterized by increased organic content of marine sediment on a global scale with accompanying positive excursions in sedimentary organic and inorganic d 13C values. To sustain the increased C exports and burial required to explain the C isotope excursion, increased supplies of nutrients to the oceans are often invoked during ocean anoxic events. The potential source of nutrients in these events is investigated in this study for Oceanic Anoxic Event 2, which spans the Cenomanian-Turonian boundary. Massive eruptions of one or more Large Igneous Provinces (LIPs) are the proposed trigger for OAE 2. The global warming associated with volcanogenic loading of carbon dioxide to the atmosphere has been associated with increased continental weathering rates during OAE 2, and by extension, enhanced nutrient supplies to the oceans. Seawater interactions with hot basalts at LIP eruption sites can further deliver ferrous iron and other reduced metals to seawater that can stimulate increased productivity in surface waters and increased oxygen demand in deep waters. The relative importance of continental and submarine weathering drivers of expanding ocean anoxia during OAE 2 are difficult to disentangle. In this paper, a box model of the marine Sr cycle is used to constrain the timing and relative magnitudes of changes in the continental weathering and hydrothermal Sr fluxes to the oceans during OAE 2 using a new high-resolution record of seawater 87Sr/86Sr ratios preserved in a marl-limestone succession from the Iona-1 core collected from the Eagle Ford Formation in Texas. The results show that seawater 87Sr/86Sr ratios change synchronously with Os isotope evidence for the onset of massive LIP volcanism 60 kyr before the positive C isotope excursion that traditionally marks the onset of OAE 2. The higher temporal resolution of the seawater Sr isotope record presented in this study warrants a detailed quantitative analysis of the changes in continental weathering and hydrothermal Sr inputs to the oceans during OAE 2. Using an ocean Sr box model, it is found that increasing the continental weathering Sr flux by  1.8-times captures the change in seawater 87Sr/86Sr recorded in the Iona-1 core. The increase in the continental weathering flux is smaller than the threefold increase estimated by studies of seawater Ca isotope changes during OAE 2, suggesting that hydrothermal forcing may have played a larger role in the development of ocean anoxic events than previously considered. 

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2. A Tale of Two LIP- (Large-Igneous Province) Induced Hyperthermals: The end-Triassic extinction (ETE) and Toarcian OAE (T-OAE)

   Whiteside, J ; Yager, J ; Tackett, L ; Schaller, M ; Olsen, P ( December 2019 , American Geophysical Union Annual Conference)

   Although many sources of atmospheric CO2 have been identified, the major sinks are best understood in a deep-time context. Here, we focus on two Large Igneous Provinces (LIPs), the Central Atlantic Magmatic Province (CAMP) situated in the low latitude humid zone ~201.6 Ma and the Karoo-Ferrar located at high southern latitudes ~183 Ma. We use soil carbonate, lithologic, δD of n-alkanes, Sr data, and modeling to examine how these eruptions, hydrological cycling, and weathering impacted global atmospheric CO2, carbon cycling, and biotic extinction at the ETE and T-OAE hyperthermals. CAMP largely erupted in the tropics, doubled atmospheric CO2 from ~2,500 – 5,000 ppm at the ETE (observed in soil carbonates with an onset <1000 and a duration of <~20 ky) and rapidly sequestered CO2 (< 2,500 ppm) as recorded in Newark Supergroup basins (eastern US). These same strata preserve variations in the lake level expression of the climatic precession cycle based on lithology and δD. High cyclicity variance tracked high pCO2 (>~4000 ppm) and drove insolation-paced increases in precipitation. Leaf wax δD shows significant variability, reflecting an enhanced hydrological cycle at the ETE with repeated sudden shifts in relative evaporation for ~1 Myr. In marine strata, 87Sr/86Sr and 187Os/188Os values track changes in pCO2, suggesting a terrestrial/marine linkage through continental weathering, CO2, and runoff. Despite the northward movement of these basins into the arid belt, our data suggest lower evaporation relative to precipitation driven by lower temperatures, consistent with lower pCO2 due to CAMP weathering, which modeling estimates to have increased 6 to 10-fold for >1.6 Myr after the eruptive phase. Release of CO2 from the Karoo-Ferrar LIP similarly enhanced the hydrological cycle as evidenced from sedimentary observations (e.g., fine-scale turbidites and debris flow deposits) in Yorkshire (UK). The onset of the carbon isotope excursion at the T-OAE lasts 0.5 Myr with a 1.5 Myr duration modulated by astronomical pacing. Our leaf wax δD from the same strata show a transient enhancement in the hydrological cycle. Although the Karoo-Ferrar has a limited drawdown potential when compared with CAMP‐type basalts because of its higher latitude location, Toarcian weathering rates may have increased 2 to 5-fold, acting as a net sink 1–2 Myr after eruptions ceased. 

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3. Biotic extinction at the Norian/Rhaetian boundary (Upper Triassic): geochemical and isotope evidence of a previously unrecognised global event

   https://doi.org/10.46427/gold2022.11474  

   Rigo, Manuel ; Onoue, Tetsuji ; Sato, Honami ; Tomimatsu, Yuki ; Soda, Katsuhito ; Godfrey, Linda ; Katz, Miriam ; Campbell, Hamish ; Tackett, Lydia ; Golding, Martyn ; et al ( October 2022 , Goldschmidt 2022 Abstract)

   turnovers culminating in the so-called End-Triassic Extinction. We attribute onset of this interval of declining diversity to unusually high volcanic activity at the Norian/Rhaetian boundary (NRB) that may have initiated the stepwise extinctions of the Late Triassic [1]. We correlate the initiation of a rapid decline in 87Sr/86Sr and 187Os/188Os seawater values [2, 3] to a negative organic carbon isotope shift, which we attribute to volcanogenic CO2 outgassing to the ocean-atmosphere system by the Angayucham large igneous province (LIP). By studying the geochemical and isotope composition of bulk rocks from different sections located at different latitudes, sides of the Pangea continent and Hemispheres, we documented an accelerated chemical weathering due to global warming by elevated CO2, which enhanced nutrient discharge to the oceans and thus greatly increased biological productivity; higher export production and oxidation of organic matter led to oceanic dysoxia to anoxia at the NRB. Biotic consequences of these climatic and environmental changes include severe extinctions of several fossil groups, such as ammonoids, bivalves and radiolarians, as has been documented worldwide [1]. 

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4. Uncovering the spatial heterogeneity of Ediacaran carbon cycling

   https://doi.org/10.1111/gbi.12222  

   Li, C. ; Hardisty, D. S. ; Luo, G. ; Huang, J. ; Algeo, T. J. ; Cheng, M. ; Shi, W. ; An, Z. ; Tong, J. ; Xie, S. ; et al ( December 2016 , Geobiology)

   Records of the Ediacaran carbon cycle (635–541 million years ago) include the Shuram excursion (SE), the largest negative carbonate carbon isotope excursion in Earth history (down to −12‰). The nature of this excursion remains enigmatic given the difficulties of interpreting a perceived extreme global decrease in the δ¹³C of seawater dissolved inorganic carbon. Here, we present carbonate and organic carbon isotope (δ¹³C_carband δ¹³C_org) records from the Ediacaran Doushantuo Formation along a proximal‐to‐distal transect across the Yangtze Platform of South China as a test of the spatial variation of theSE. Contrary to expectations, our results show that the magnitude and morphology of this excursion and its relationship with coexisting δ¹³C_orgare highly heterogeneous across the platform. Integrated geochemical, mineralogical, petrographic, and stratigraphic evidence indicates that theSEis a primary marine signature. Data compilations demonstrate that theSEwas also accompanied globally by parallel negative shifts of δ³⁴S of carbonate‐associated sulfate (CAS) and increased⁸⁷Sr/⁸⁶Sr ratio and coastalCASconcentration, suggesting elevated continental weathering and coastal marine sulfate concentration during theSE. In light of these observations, we propose a heterogeneous oxidation model to explain the high spatial heterogeneity of theSEand coexisting δ¹³C_orgrecords of the Doushantuo, with likely relevance to theSEin other regions. In this model, we infer continued marine redox stratification through theSEbut with increased availability of oxidants (e.g., O₂and sulfate) limited to marginal near‐surface marine environments. Oxidation of limited spatiotemporal extent provides a mechanism to drive heterogeneous oxidation of subsurface reduced carbon mostly in shelf areas. Regardless of the mechanism driving theSE, future models must consider the evidence for spatial heterogeneity in δ¹³C presented in this study.

    

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5. Patterns of local and global redox variability during the Cenomanian–Turonian Boundary Event (Oceanic Anoxic Event 2) recorded in carbonates and shales from central Italy

   https://doi.org/10.1111/sed.12352  

   Owens, Jeremy D. ; Lyons, Timothy W. ; Hardisty, Dalton S. ; Lowery, Chris M. ; Lu, Zunli ; Lee, Bridget ; Jenkyns, Hugh C. ; Heimhofer, ed., Ulrich ( January 2017 , Sedimentology)

   Careful evaluation of the local geochemical conditions in past marine settings can provide a window to the average redox state of the global ocean during episodes of extensive organic carbon deposition. These comparisons aid in identifying the interplay between climate and biotic feedbacks contributing to and resulting from these events. Well‐documented examples are known from the Mesozoic Era, which is characterized by episodes of widespread organic carbon deposition known as Oceanic Anoxic Events. This organic carbon burial typically leads to coeval positive carbon‐isotope excursions. Geochemical data are presented here for several palaeoredox proxies (Cr/Ti, V, Mo, Zn, Mn, Fe speciation, I/Ca and sulphur isotopes) from a section exposed at Furlo in the Marche–Umbrian Apennines of Italy that spans the Cenomanian–Turonian boundary. Here, Oceanic Anoxic Event 2 is represented by aca1 m thick radiolarian‐rich millimetre‐laminated organic‐rich shale known locally as the Bonarelli Level. Iron speciation data for thin organic‐rich intervals observed below the Bonarelli Level imply a local redox shift going into the Oceanic Anoxic Event, with ferruginous conditions (i.e. anoxic with dissolved ferrous iron) transiently developed prior to the event and euxinia (i.e. anoxic and sulphidic bottom waters) throughout the event itself. Pre‐Oceanic Anoxic Event enrichments of elements sensitive to anoxic water columns were due to initial development of locally ferruginous bottom waters as a precursor to the event. However, the greater global expanse of dysoxic to euxinic conditions during the Oceanic Anoxic Event greatly reduced redox‐sensitive trace‐metal concentrations in seawater. Pyrite sulphur isotopes document a positive excursion during the Oceanic Anoxic Event. Carbonate I/Ca ratios were generally low, suggesting locally reduced bottom‐water oxygen conditions preceding the event and relatively increased oxygen concentrations post‐event. Combined, the Furlo geochemical data suggest a redox‐stratified water column with oxic surface waters and a shallow chemocline overlying locally ferruginous bottom waters preceding the event, globally widespread euxinic bottom waters during the Oceanic Anoxic Event, followed by chemocline shallowing but sustained local redox stratification following the event.

    

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