Oxygen levels in the atmosphere and ocean have changed dramatically over Earth history, with major impacts on marine life. Because the early part of Earth’s history lacked both atmospheric oxygen and animals, a persistent co-evolutionary narrative has developed linking oxygen change with changes in animal diversity. Although it was long believed that oxygen rose to essentially modern levels around the Cambrian period, a more muted increase is now believed likely. Thus, if oxygen increase facilitated the Cambrian explosion, it did so by crossing critical ecological thresholds at low O2. Atmospheric oxygen likely remained at low or moderate levels through the early Paleozoic era, and this likely contributed to high metazoan extinction rates until oxygen finally rose to modern levels in the later Paleozoic. After this point, ocean deoxygenation (and marine mass extinctions) is increasingly linked to large igneous province eruptions—massive volcanic carbon inputs to the Earth system that caused global warming, ocean acidification, and oxygen loss. Although the timescales of these ancient events limit their utility as exact analogs for modern anthropogenic global change, the clear message from the geologic record is that large and rapid CO2 injections into the Earth system consistently cause the same deadly trio of stressors that are observed today. The next frontier in understanding the impact of oxygen changes (or, more broadly, temperature-dependent hypoxia) in deep time requires approaches from ecophysiology that will help conservation biologists better calibrate the response of the biosphere at large taxonomic, spatial, and temporal scales.
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Late inception of a resiliently oxygenated upper ocean
Rising oceanic and atmospheric oxygen levels through time have been crucial to enhanced habitability of surface Earth environments. Few redox proxies can track secular variations in dissolved oxygen concentrations ([O2]) around threshold levels for metazoan survival in the upper ocean. We present an extensive compilation of iodine to calcium ratios (I/Ca) in marine carbonates. Our record supports a major rise in atmospheric pO2 at ~400 million years ago (Ma), and reveals a step-change in the oxygenation of the upper ocean to relatively sustainable near-modern conditions at ~200 Ma. An Earth system model demonstrates that a shift in organic matter remineralization to greater depths, which may have been due to increasing size and biomineralization of eukaryotic plankton, likely drove the I/Ca signals at ~200 Ma
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- PAR ID:
- 10065856
- Author(s) / Creator(s):
- ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; more »
- Date Published:
- Journal Name:
- Science
- ISSN:
- 0036-8075
- Page Range / eLocation ID:
- eaar5372
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Lyons, T. ; Turchyn, A. ; Reinhard, C. (Ed.)How oxygen levels in Earth’s atmosphere and oceans evolved has always been a central question in Earth System Science. Researchers have developed numerous tracers to tackle this question, utilizing geochemical characteristics of different elements. Iodine incorporated in calcium carbonate (including biogenic) minerals, reported as I/Ca, is a proxy for dissolved oxygen in seawater. Here we review the rationale behind this proxy, its recent applications, and some potential future research directions.more » « less
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Abstract The iodine to calcium ratio in carbonate (I/Ca) has been widely used to indicate ocean oxygenation level in the past. Given the volatility of iodine, I/Ca has been measured in alkaline solutions in previous studies. However, this limits the application of I/Ca with other element/Ca (El/Ca) proxies at the same time and in the same foraminifera because other El/Ca data are preferably analyzed in acidic solutions. This study assesses the reliability of I/Ca measurements in acidic solutions measured with other El/Ca as well as the effects of different sample pre‐treatments on measured foraminiferal I/Ca. Our results show that when samples are measured within hours of prepaparation, the pH of the final solution has an insignificant effect on I/Ca measurements of a carbonate reference material JCp‐1 and a multi‐element standard solution, consistent with the slow kinetics of iodine volatilization. We find, however, that low pH possibly reduces the measured I/Ca in foraminiferal tests in some samples. Our experiments also suggest a resolvable effect of reductive cleaning, yielding lower foraminiferal I/Ca compared to without reductive cleaning. The HNO3concentration used to dissolve foraminiferal shells has a negligible effect. Despite the different solution pHs and cleaning and dissolving methods, our core top planktic I/Ca data are able to differentiate well‐oxygenated from oxygen‐depleted waters in the upper ocean, and after correcting for cleaning effect, our data are generally consistent with the published studies that analyzed I/Ca without reductive cleaning and in basic solutions. This study shows that measurements of I/Ca within hours of sample dissolutions yield reliable planktic I/Ca data, while also allowing the acquisition of other El/Ca values for paleoceanographic studies.
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The evolution of oxygen cycles on Earth’s surface has been regulated by the balance between molecular oxygen production and consumption. The Neoproterozoic–Paleozoic transition likely marks the second rise in atmospheric and oceanic oxygen levels, widely attributed to enhanced burial of organic carbon. However, it remains disputed how marine organic carbon production and burial respond to global environmental changes and whether these feedbacks trigger global oxygenation during this interval. Here, we report a large lithium isotopic and elemental dataset from marine mudstones spanning the upper Neoproterozoic to middle Cambrian [~660 million years ago (Ma) to 500 Ma]. These data indicate a dramatic increase in continental clay formation after ~525 Ma, likely linked to secular changes in global climate and compositions of the continental crust. Using a global biogeochemical model, we suggest that intensified continental weathering and clay delivery to the oceans could have notably increased the burial efficiency of organic carbon and facilitated greater oxygen accumulation in the earliest Paleozoic oceans.more » « less
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Abstract. Iodine (I) abundance in marine carbonates (measured as an elemental ratio with calcium, I / Ca) is of broad interest as a proxy for local/regional ocean redox. This connection arises because the speciation of iodine in seawater, the balance between iodate (IO3-) and iodide (I−), is sensitive to the prevalence of oxic vs. anoxic conditions. However, although I / Ca ratios are increasingly commonly being measured in ancient carbonate samples, a fully quantitative interpretation of this proxy requires the availability of a mechanistic interpretative framework for the marine iodine cycle that can account for the extent and intensity of ocean deoxygenation in the past. Here we present and evaluate a representation of marine iodine cycling embedded in an Earth system model (“cGENIE”) against both modern and paleo-observations. In this framework, we account for IO3- uptake and release of I− through the biological pump, the reduction in ambient IO3- to I− in the water column, and the re-oxidation of I− to IO3-. We develop and test a variety of different plausible mechanisms for iodine reduction and oxidation transformation and contrast model projections against an updated compilation of observed dissolved IO3- and I− concentrations in the present-day ocean. By optimizing the parameters controlling previously proposed mechanisms involved in marine iodine cycling, we find that we can obtain broad matches to observed iodine speciation gradients in zonal surface distribution, depth profiles, and oxygen-deficient zones (ODZs). However, we also identify alternative, equally well performing mechanisms which assume a more explicit mechanistic link between iodine transformation and environment – an ambiguity that highlights the need for more process-based studies on modern marine iodine cycling. Finally, to help distinguish between competing representations of the marine iodine cycle and because our ultimate motivation is to further our ability to reconstruct ocean oxygenation in the geological past, we conducted “plausibility tests” of different model schemes against available I / Ca measurements made on Cretaceous carbonates – a time of substantially depleted ocean oxygen availability compared to modern and hence a strong test of our model. Overall, the simultaneous broad match we can achieve between modeled iodine speciation and modern observations, and between forward proxy modeled I / Ca and geological elemental ratios, supports the application of our Earth system modeling in simulating the marine iodine cycle to help interpret and constrain the redox evolution of past oceans.
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1126/science.aar5372
