The potential of carbon capture through mineral weathering

Noah Planavsky is an Associate Professor in the Department of Earth and Planetary Sciences. He joined the faculty in 2012 after doing graduate work at University of California, Riverside. He is an isotope geochemist that works on environmental change in Earth’s past, present, and future. His work combines field studies, analytical chemistry, and geochemical modeling. He has worked extensively on atmospheric evolution—with a particular focus on changes in oxygen and carbon dioxide concentrations. Current projects focus on changes in ocean oxygen levels and on the potential for carbon capture through enhanced mineral weathering in marine and terrestrial environments

Long-term sedimentary recycling of rare sulphur isotope anomalies

The accumulation of substantial quantities of O_2 in the atmosphere has come to control the chemistry and ecological structure of Earth’s surface. Non-mass-dependent (NMD) sulphur isotope anomalies in the rock record are the central tool used to reconstruct the redox history of the early atmosphere. The generation and initial delivery of these anomalies to marine sediments requires low partial pressures of atmospheric O_2 (PO_2; refs 2, 3), and the disappearance of NMD anomalies from the rock record 2.32 billion years ago is thought to have signalled a departure from persistently low atmospheric oxygen levels (less than about 10^(−5) times the present atmospheric level) during approximately the first two billion years of Earth’s history. Here we present a model study designed to describe the long-term surface recycling of crustal NMD anomalies, and show that the record of this geochemical signal is likely to display a ‘crustal memory effect’ following increases in atmospheric PO_2 above this threshold. Once NMD anomalies have been buried in the upper crust they are extremely resistant to removal, and can be erased only through successive cycles of weathering, dilution and burial on an oxygenated Earth surface. This recycling results in the residual incorporation of NMD anomalies into the sedimentary record long after synchronous atmospheric generation of the isotopic signal has ceased, with dynamic and measurable signals probably surviving for as long as 10–100 million years subsequent to an increase in atmospheric PO_2 to more than 10^(−5) times the present atmospheric level. Our results can reconcile geochemical evidence for oxygen production and transient accumulation with the maintenance of NMD anomalies on the early Earth, and suggest that future work should investigate the notion that temporally continuous generation of new NMD sulphur isotope anomalies in the atmosphere was likely to have ceased long before their ultimate disappearance from the rock record

Not so non-marine? Revisiting the Stoer Group and the Mesoproterozoic biosphere

Funding for this project was provided by the NASA postdoctoral program (EES), the Lewis and Clark Fund (EES), an NSERC PGS-D grant (EJB), the NSF ELT (TWL, NJP) and FESD (TWL) programs, and the NASA Astrobiology Institute (TWL, NJP).The Poll a’Mhuilt Member of the Stoer Group (Torridonian Supergroup) in Scotland has been heralded as a rare window into the ecology of Mesoproterozoic terrestrial environments. Its unusually high molybdenum concentrations and large sulphur isotope fractionations have been used as evidence to suggest that lakes 1.2 billion years ago were better oxygenated and enriched in key nutrients relative to contemporaneous oceans, making them ideal habitats for the evolution of eukaryotes. Here we show with new Sr and Mo isotope data, supported by sedimentological evidence, that the depositional setting of this unit was likely connected to the ocean and that the elevated Mo and S contents can be explained by evapo-concentration of seawater. Thus, it remains unresolved if Mesoproterozoic lakes were important habitats for early eukaryotic life.Publisher PDFPeer reviewe

A tool for assessing the sensitivity of soil-based approaches for quantifying enhanced weathering: a US case study

Enhanced weathering (EW) of silicate rocks spread onto managed lands as agricultural amendments is a promising carbon dioxide removal (CDR) approach. However, there is an obvious need for the development of tools for Measurement, Reporting, and Verification (MRV) before EW can be brought to scale. Shifts in the concentration of mobile elements measured in the solid phase of soils after application of EW feedstocks can potentially be used to track weathering and provide an estimate of the initial carbon dioxide removal of the system. To measure feedstock dissolution accurately it is necessary to control for the amount of feedstock originally present in the sample being analyzed. This can be achieved by measuring the concentration of immobile detrital elements in soil samples after feedstock addition. However, the resolvability of a signal using a soil mass balance approach depends on analytical uncertainty, the ability to accurately sample soils, the amount of feedstock relative to the amount of initial soil in a sample, and on the fraction of feedstock that has dissolved. Here, we assess the viability of soil-based mass-balance approaches across different settings. Specifically, we define a metric for tracer-specific resolvability of feedstock mass addition (φ) and calculate the feedstock application rates (a) and dissolution fractions (b) required to resolve EW. Applying calculations of a, b, and φ to a gridded soil database from the contiguous USA in combination with known compositions of basalt and peridotite feedstocks demonstrates the importance of adequately capturing field heterogeneity in soil elemental concentrations. While EW signals should be resolvable after ~1–3 years of basalt feedstock addition at common application rates for most agricultural settings with adequate sampling protocols, resolving EW in the field is likely to be challenging if uncertainties in tracer concentrations derived from field-scale heterogeneity and analytical error exceed 10%. Building from this framework, we also present a simple tool for practitioners to use to assess the viability of carrying out soil-based EW MRV in a deployment-specific context

Persistent global marine euxinia in the early Silurian

The second pulse of the Late Ordovician mass extinction occurred around the Hirnantian-Rhuddanian boundary (~444 Ma) and has been correlated with expanded marine anoxia lasting into the earliest Silurian. Characterization of the Hirnantian ocean anoxic event has focused on the onset of anoxia, with global reconstructions based on carbonate δ238U modeling. However, there have been limited attempts to quantify uncertainty in metal isotope mass balance approaches. Here, we probabilistically evaluate coupled metal isotopes and sedimentary archives to increase constraint. We present iron speciation, metal concentration, δ98Mo and δ238U measurements of Rhuddanian black shales from the Murzuq Basin, Libya. We evaluate these data (and published carbonate δ238U data) with a coupled stochastic mass balance model. Combined statistical analysis of metal isotopes and sedimentary sinks provides uncertainty-bounded constraints on the intensity of Hirnantian-Rhuddanian euxinia. This work extends the duration of anoxia to >3 Myrs – notably longer than well-studied Mesozoic ocean anoxic events

Constraining Prebiotic Chemistry Through a Better Understanding of Earth's Earliest Environments

Any search for present or past life beyond Earth should consider the initial processes and related environmental controls that might have led to its start. As on Earth, such an understanding lies well beyond how simple organic molecules become the more complex biomolecules of life, because it must also include the key environmental factors that permitted, modulated, and most critically facilitated the prebiotic pathways to life's emergence. Moreover, we ask how habitability, defined in part by the presence of liquid water, was sustained so that life could persist and evolve to the point of shaping its own environment. Researchers have successfully explored many chapters of Earth's coevolving environments and biosphere spanning the last few billion years through lenses of sophisticated analytical and computational techniques, and the findings have profoundly impacted the search for life beyond Earth. Yet life's very beginnings during the first hundreds of millions of years of our planet's history remain largely unknown--despite decades of research. This report centers on one key point: that the earliest steps on the path to life's emergence on Earth were tied intimately to the evolving chemical and physical conditions of our earliest environments. Yet, a rigorous, interdisciplinary understanding of that relationship has not been explored adequately and once better understood will inform our search for life beyond Earth. In this way, studies of the emergence of life must become a truly interdisciplinary effort, requiring a mix that expands the traditional platform of prebiotic chemistry to include geochemists, atmospheric chemists, geologists and geophysicists, astronomers, mission scientists and engineers, and astrobiologists.Comment: Planetary science and astrobiology community white paper submitted to the National Academy of Science

No evidence for high atmospheric oxygen levels 1,400 million years ago

Zhang et al. (1) recently proposed atmospheric oxygen levels of ∼4% present atmospheric levels (PAL) based on modeling a paleoenvironment reconstructed from trace metal and biomarker data from the 1,400 Ma Xiamaling Formation in China. Intriguingly, this pO2 level is above the threshold oxygen requirements of basal animals and clashes with evidence for atmospheric oxygen levels <<1% PAL in the mid-Proterozoic (2). However, there are fundamental problems with the inorganic and organic geochemical work presented by Zhang et al. (1)

Chromium isotope fractionation during subduction-related metamorphism, black shale weathering, and hydrothermal alteration

© The Author(s), 2016. This is the author's version of the work and is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Chemical Geology 423 (2016): 19-33, doi:10.1016/j.chemgeo.2016.01.003.Chromium (Cr) isotopes are an emerging proxy for redox processes at Earth’s surface. However, many geological reservoirs and isotope fractionation processes are still not well understood. The purpose of this contribution is to move forward our understanding of (1) Earth’s high temperature Cr isotope inventory and (2) Cr isotope fractionations during subduction-related metamorphism, black shale weathering and hydrothermal alteration. The examined basalts and their metamorphosed equivalents yielded δ53Cr values falling within a narrow range of -0.12±0.13‰ (2SD, n=30), consistent with the previously reported range for the bulk silicate Earth (BSE). Compilations of currently available data for fresh silicate rocks (43 samples), metamorphosed silicate rocks (50 samples), and mantle chromites (39 samples) give δ53Cr values of -0.13±0.13‰, -0.11±0.13‰, and -0.07±0.13‰, respectively. Although the number of high-temperature samples analyzed has tripled, the originally proposed BSE range appears robust. This suggests very limited Cr isotope fractionation under high temperature conditions. Additionally, in a highly altered metacarbonate transect that is representative of fluid-rich regional metamorphism, we did not find resolvable variations in δ53Cr, despite significant loss of Cr. This work suggests that primary Cr isotope signatures may be preserved even in instances of intense metamorphic alteration at relatively high fluid-rock ratios. Oxidative weathering of black shale at low pH creates isotopically heavy mobile Cr(VI). However, a significant proportion of the Cr(VI) is apparently immobilized near the weathering surface, leading to local enrichment of isotopically heavy Cr (δ53Cr values up to ~0.5‰). The observed large Cr isotope variation in the black shale weathering profile provides indirect evidence for active manganese oxide formation, which is primarily controlled by microbial activity. Lastly, we found widely variable δ53Cr (-0.2‰ to 0.6‰) values in highly serpentinized peridotites from ocean drilling program drill cores and outcropping ophiolite sequences. The isotopically heavy serpentinites are most easily explained through a multi-stage alteration processes: Cr loss from the host rock under oxidizing conditions, followed by Cr enrichment under sulfate reducing conditions. In contrast, Cr isotope variability is limited in mildly altered mafic oceanic crust.Funding for this research was provided by Agouron Institute to XLW, National Science Foundation (NSF) EAR-0105927 and EAR-1250269 to JJA, and NSF EAR-1324566 to ES. NJP and CTR acknowledge funding from the Alternative Earths NAI.2017-01-1