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The tropical Pacific is one of the largest ocean regions on Earth where the trace element iron limits new primary production and therefore the efficiency of carbon export to the deep sea. Although there is a long history of marine biogeochemical research in the tropical Pacific, recent advancements using GEOTRACES key parameters such as iron and nitrate isotopes (nitrate δ15N and δ18O) make this a good time to review the current understanding of tropical Pacific nitrate dynamics—how both regional subsurface nitrate characteristics and surface ocean nitrate utilization change with time. While this article provides a comprehensive overview of the biological, chemical, and physical processes shaping equatorial Pacific subsurface-to-surface nutrients, it principally explores the findings from the first nitrate isotope time series in iron-limited high nutrient, low chlorophyll waters. Results indicate that the preferential recycling of bioavailable iron within the euphotic zone is required to explain even the lowest observed nitrate utilization in the eastern equatorial Pacific (EEP). Furthermore, because seasonal-to-interannual nitrate utilization variability in the EEP cannot be driven by changes in iron supply, this work argues that iron recycling (and therefore bioavailable iron) is modulated by upwelling rate changes, creating a predicted and recently observed spectrum of iron limitation in the iron-limited EEP surface waters. In other words, upper ocean physics overwhelmingly dominates seasonal-to-interannual nitrate utilization in the iron-​limited EEP. This new understanding of nitrate utilization in iron-limited waters helps to explain long-term changes in past equatorial Pacific nitrate utilization obtained via sedimentary proxy records and potentially complicates the efficacy of future iron fertilization of the equatorial Pacific. 

Abstract Measuring, reporting, and verification (MRV) of ocean-based carbon dioxide removal (CDR) presents challenges due to the dynamic nature of the ocean and the complex processes influencing marine carbonate chemistry. Given these challenges, finding the optimal sampling strategies and suite of parameters to be measured is a timely research question. While traditional carbonate parameters such as total alkalinity (TA), dissolved inorganic carbon (DIC), pH, and seawater pCO2 are commonly considered, exploring the potential of carbon isotopes for quantifying additional CO2 uptake remains a relatively unexplored research avenue. In this study, we use a coupled physical-biogeochemical model of the California Current System (CCS) to run a suite of Ocean Alkalinity Enhancement (OAE) simulations. The physical circulation for the CCS is generated using a nested implementation of the Regional Ocean Modeling System (ROMS) with an outer domain of 1/10 ̊ (~10 km) and an inner domain of 1/30 ̊ (~3 km) resolution. The biogeochemical model, NEMUCSC, is a customized version of the North Pacific Ecosystem Model for Understanding Regional Oceanography (NEMURO) that includes carbon cycling and carbon isotopes. The CCS is one of four global eastern boundary upwelling systems characterized by high biological activity and CO2 concentrations. Consequently, the CCS represents an essential test case for investigating the efficacy and potential side effects of OAE deployments. The study aims to address two key questions: (1) the relative merit of OAE to counter ocean acidification versus the additional sequestration of CO2 from the atmosphere, and (2) the footprint of potentially harmful seawater chemistry adjacent to OAE deployments. We plan to leverage these high-resolution model results to competitively evaluate different MRV strategies, with a specific focus on analyzing the spatiotemporal distribution of carbon isotopic signatures following OAE. In this talk, we will showcase our initial results and discuss challenges in integrating high-resolution regional modeling into models of the global carbon cycle. More broadly, this work aims to provide insights into the plausibility of OAE as a climate solution that maintains ocean health and to inform accurate quantification of carbon uptake for MRV purposes. https://agu.confex.com/agu/OSM24/prelim.cgi/Paper/1491096 

Abstract In this work, we utilize a transect of core top, mid- to late Holocene, sediments from the Eastern Siberian Sea to the central Arctic Ocean, spanning gradients in upper-ocean water column properties, to examine regional planktic foraminiferal species abundances and geochemistry. We present species- and morphotype-specific foraminiferal assemblages at these sites and stable isotope analyses of neogloboquadrinids. We find little variation in planktic species populations, and only small variations in N. pachyderma morphotype distributions, between sites. Spatial averages of N. pachyderma morphotype and N. incompta δ18O values show no significant differences, suggesting a similar calcification depth for all morphotypes of N. pachyderma and N. incompta across our sites, which we estimate to be between ∼ 50–150 m. Values of δ18O of a group of unencrusted specimens delineate a shallower calcification habitat. Neogloboquadrina pachyderma-2 Mg/Ca values yield temperatures outside the range of observations using available calibration equations, pointing toward the need for more Arctic-specific Mg/Ca-temperature calibrations. 

The observation of extremely low radiocarbon content / old radiocarbon ages (>4000 years old) in the intermediate-depth ocean during the last ice age draws attention to our incomplete understanding of ocean carbon cycling. For example, glacial-interglacial seawater 14C anomalies near the Gulf of California have been explained by both the advection from a 14C-depleted abyssal source and local geologic carbon flux. To provide insight to this the origin of the seawater 14C anomalies, we have produced several new records of glacial-interglacial intermediate water (i.e., 14C, δ11B, δ18O, and δ13C) in waters that are “upstream” and “downstream” of the Gulf of California. These observations plus geochemical modeling allow us to: (1) Answer whether the old seawater 14C ages are advected or produced locally; (2) Identify the approximate chemical make-up of this carbon; and (3) Consider the role of known sedimentary processes in this carbon flux to the ocean. (Note that several sites have age model controls based on terrestrial plant 14C ages, providing more confidence in our results.) Our new measurements and modeling indicate that the well-established >4000-year-old seawater 14C anomalies observed near known seafloor volcanism in the Gulf of California are not present “upstream,” indicating that this carbon flux results from a “local” geologic carbon. Furthermore, based on our new benthic foraminifera δ11B measurements, this local carbon Blux does not appear to affect seawater pH. Finally, we suggest several potential geologic carbon source(s) that could explain the anomalously old seawater 14C ages, the relatively unremarkable changes in seawater δ13C, and the essentially negligible change in seawater pH. 

As companies begin selling credits for marine carbon dioxide removal in largely unregulated marketplaces, scientists must develop standards for assessing the effectiveness of removal methods. 

A compilation of radiocarbon measurements is used to characterize deep-sea overturning since the last ice age. 

Gas exchange between the atmosphere and ocean interior profoundly impacts global climate and biogeochemistry. However, our understanding of the relevant physical processes remains limited by a scarcity of direct observations. Dissolved noble gases in the deep ocean are powerful tracers of physical air-sea interaction due to their chemical and biological inertness, yet their isotope ratios have remained underexplored. Here, we present high-precision noble gas isotope and elemental ratios from the deep North Atlantic (~32°N, 64°W) to evaluate gas exchange parameterizations using an ocean circulation model. The unprecedented precision of these data reveal deep-ocean undersaturation of heavy noble gases and isotopes resulting from cooling-driven air-to-sea gas transport associated with deep convection in the northern high latitudes. Our data also imply an underappreciated and large role for bubble-mediated gas exchange in the global air-sea transfer of sparingly soluble gases, including O 2 , N 2 , and SF 6 . Using noble gases to validate the physical representation of air-sea gas exchange in a model also provides a unique opportunity to distinguish physical from biogeochemical signals. As a case study, we compare dissolved N 2 /Ar measurements in the deep North Atlantic to physics-only model predictions, revealing excess N 2 from benthic denitrification in older deep waters (below 2.9 km). These data indicate that the rate of fixed N removal in the deep Northeastern Atlantic is at least three times higher than the global deep-ocean mean, suggesting tight coupling with organic carbon export and raising potential future implications for the marine N cycle.