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1. 210Po and 210Pb distributions during a phytoplankton bloom in the North Atlantic: Implications for POC export.

   Horowitz, EJ; Cochran, JK; Bacon, MP; Hirschberg, DJ (June 2020, Deep sea research)

   null (Ed.)

   During the North Atlantic Bloom Experiment (NABE) of the Joint Global Ocean Flux Study (JGOFS), water column sampling for particulate and dissolved 210Po and 210Pb was performed four times (26 April and 4, 20, 30 May 1989) during a month-long Lagrangian time-series occupation of the NABE site, as well as one-time samplings at stations during transit to and from the site. There are few prior studies documenting short-term changes in 210Po and 210Pb profiles over the course of a phytoplankton bloom, and we interpret the profiles in terms of the classical “steady-state” (SS) approach used in most studies, as well as by using a non-steady state approach suggested by the temporal evolution of the profiles. Changes in 210Po profiles during a bloom are expectable as this radionuclide is scavenged and exported. During NABE, 210Pb profiles also displayed non-steady state, with significant increases in upper water column inventory occurring midway through the experiment. Export of 210Po from the upper 150 m using the classic “steady- state” model shows increases from 0.1 ± 1.7 dpm m-2 d-1 to 84.8 ± 6.2 dpm m-2 d-1 over the ~1 month occupation. Application of a non-steady state model, including changes in both 210Pb and 210Po profiles, gives higher 210Po export fluxes. Detailed depth profiles of particulate organic carbon (>0.8 μm) and particulate 210Po (>0.4 μm) are available from the 20 and 30 May samplings and show maxima in POC/Po at ~37 m. Applying the POC/210Po ratios at 150 m to the “steady state” 210Po fluxes yields POC export from the upper 150 m of 8.5 mmol m-2 d-1 on 20 May and 6.3 mmol C m-2 d-1 on 30 May. The non-steady state model applied to the interval 20 to 30 May yields POC export of 24.3 mmol C m-2 d-1. The non-steady state (NSS) 210Po-derived POC fluxes are comparable to, but somewhat less than, those estimated previously from 234Th/238U disequilibrium for the same time interval (37.3 and 45.0 mmol m-2 d-1, depending on the POC/Th ratio used). In comparison, POC fluxes measured with a floating sediment trap deployed at 150 m from 20 to 30 May were 11.6 mmol m-2 d-1. These results suggest that non-steady state Po-derived POC fluxes during the NABE agree well with those derived from 234Th/238U disequilibrium and agree with sediment trap fluxes within a factor of ~2. However, unlike the 234Th-POC flux proxy, non-steady stage changes in profiles of 210Pb, the precursor of 210Po, must be considered. 

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2. Quantifying 210Po/210Pb disequilibrium in seawater: A Comparison of two precipitation methods with differing results.

   https://doi.org/doi:10.3389/fmars2021.684484  

   Roca-Martí, M; Puigcorbé, V; Castrillejo, M; Casacuberta, N; Garcia-Orellana, J; Cochran, JK; Masqué, P (June 2021, Frontiers in marine science)

   null (Ed.)

   The disequilibrium between lead-210 (210Pb) and polonium-210 (210Po) is increasingly used in oceanography to quantify particulate organic carbon (POC) export from the upper ocean. This proxy is based on the deficits of 210Po typically observed in the upper water column due to the preferential removal of 210Po relative to 210Pb by sinking particles. Yet, a number of studies have reported unexpected large 210Po deficits in the deep ocean indicating scavenging of 210Po despite its radioactive mean life of ~200 days. Two precipitation methods, Fe(OH)3 and Co-APDC, are typically used to concentrate Pb and Po from seawater samples, and deep 210Po deficits raise the question whether this feature is biogeochemically consistent or there is a methodological issue. Here, we present a compilation of 210Pb and 210Po studies that suggests that 210Po deficits at depths >300 m are more often observed in studies where Fe(OH)3 is used to precipitate Pb and Po from seawater, than in those using Co-APDC (in 68 versus 33% of the profiles analyzed for each method, respectively). In order to test whether 210Po/210Pb disequilibrium can be partly related to a methodological artifact, we directly compared the total activities of 210Pb and 210Po in four duplicate ocean depth-profiles determined by using Fe(OH)3 and Co-APDC on unfiltered seawater samples. While both methods produced the same 210Pb activities, results from the Co- APDC method showed equilibrium between 210Pb and 210Po below 100 m, whereas the Fe(OH)3 method resulted in activities of 210Po significantly lower than 210Pb throughout the entire water column. These results show that 210Po deficits in deep waters, but also in the upper ocean, may be greater when calculated using a commonly used Fe(OH)3 protocol. This finding has potential implications for the use of the 210Po/210Pb pair as a tracer of particle export in the oceans because 210Po (and thus POC) fluxes calculated using Fe(OH)3 on unfiltered seawater samples may be overestimated. Recommendations for future research are provided based on the possible reasons for the discrepancy in 210Po activities between both analytical methods. 

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3. Hydrothermal Plumes Act as a Regional Boundary Sink of ²³⁰ Th in the Equatorial Pacific

   https://doi.org/10.1029/2024GB008219  

   Redmond, N A; Hayes, C T; Anderson, R F; Black, E E; Edwards, R L; Fleisher, M Q; Li, X; Lam, P J; Mateos, K C (April 2025, Global Biogeochemical Cycles)

   Abstract An important role in the cycling of marine trace elements is scavenging, their adsorption and removal from the water column by sinking particles. Boundary scavenging occurs when areas of strong particle flux drive preferential removal of the trace metals at locations of enhanced scavenging. Due to its uniform production and quick burial via scavenging,²³⁰Th is used to assess sedimentary mass fluxes; however, these calculations are potentially biased near regions where net lateral transport of dissolved²³⁰Th violates the assumption that the flux of particulate²³⁰Th to the seabed equals its rate of production in the water column. Here, we present a water column transect of dissolved²³⁰Th along 152° W between Alaska and Tahiti (GEOTRACES GP15), where we examine²³⁰Th profiles across multiple biogeochemical provinces and, novelly, the lateral transport of²³⁰Th to distal East Pacific Rise hydrothermal plumes. We observed a strong relationship between the slope of dissolved²³⁰Th concentration‐depth profiles and suspended particle matter inventory in the upper‐mid water column, reinforcing the view that biogenic particle mass flux sets the background²³⁰Th distribution in open ocean settings. We find that, instead of the region of enhanced particle flux around the equator, hydrothermal plumes act as a regional boundary sink of²³⁰Th. At 152° W, we found that the flux‐to‐production ratio, and thereby error in²³⁰Th‐normalized sediment flux, is between 0.80 and 1.50 for hydrothermal water, but the error is likely larger approaching the East Pacific Rise. 

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4. Quantifying N2 fixation and its contribution to export production near the Tonga-Kermadec Arc using nitrogen isotope budgets

   https://doi.org/10.3389/fmars.2023.1249115  

   Forrer, Heather J.; Bonnet, Sophie; Thomas, Rachel K.; Grosso, Olivier; Guieu, Cecile; Knapp, Angela N. (October 2023, Frontiers in Marine Science)

   The spatial distribution of marine di-nitrogen (N₂) fixation informs our understanding of the sensitivities of this process as well as the potential for this new nitrogen (N) source to drive export production, influencing the global carbon (C) cycle and climate. Using geochemically-derived δ¹⁵N budgets, we quantified rates of N₂fixation and its importance for supporting export production at stations sampled near the southwest Pacific Tonga-Kermadec Arc. Recent observations indicate that shallow (<300 m) hydrothermal vents located along the arc provide significant dissolved iron to the euphotic zone, stimulating N₂fixation. Here we compare measurements of water column δ¹⁵N_NO3+NO2with sinking particulate δ¹⁵N collected by short-term sediment traps deployed at 170 m and 270 m at stations in close proximity to subsurface hydrothermal activity, and the δ¹⁵N of N₂fixation. Results from the δ¹⁵N budgets yield high geochemically-based N₂fixation rates (282 to 638 µmol N m^-2d^-1) at stations impacted by hydrothermal activity, supporting 64 to 92% of export production in late spring. These results are consistent with contemporaneous¹⁵N₂uptake rate estimates and molecular work describing highTrichodesmiumspp. and other diazotroph abundances associated with elevated N₂fixation rates. Further, the δ¹⁵N of sinking particulate N collected at 1000 m over an annual cycle revealed sinking fluxes peaked in the summer and coincided with the lowest δ¹⁵N, while lower winter sinking fluxes had the highest δ¹⁵N, indicating isotopically distinct N sources supporting export seasonally, and aligning with observations from most other δ¹⁵N budgets in oligotrophic regions. Consequently, the significant regional N₂fixation input to the late spring/summer Western Tropical South Pacific results in the accumulation of low-δ¹⁵N_NO3+NO2in the upper thermocline that works to lower the elevated δ¹⁵N_NO3+NO2generated in the oxygen deficient zones in the Eastern Tropical South Pacific. 

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5. Controls on Dissolved Barium and Radium‐226 Distributions in the Pacific Ocean Along GEOTRACES GP15

   https://doi.org/10.1029/2023GB008005  

   Le_Roy, Emilie; Charette, Matthew A; Henderson, Paul B; Shiller, Alan M; Moore, Willard S; Kemnitz, Nathaniel; Hammond, Douglas E; Horner, Tristan J (June 2024, Global Biogeochemical Cycles)

   Abstract Radium‐226(²²⁶Ra) and barium (Ba) exhibit similar chemical behaviors and distributions in the marine environment, serving as valuable tracers of water masses, ocean mixing, and productivity. Despite their similar distributions, these elements originate from distinct sources and undergo disparate biogeochemical cycles, which might complicate the use of these tracers. In this study, we investigate these processes by analyzing a full‐depth ocean section of²²⁶Ra activities (T_1/2 = 1,600 years) and barium concentrations obtained from samples collected along the US GEOTRACES GP15 Pacific Meridional Transect during September–November 2018, spanning from Alaska to Tahiti. We find that surface waters possess low levels of²²⁶Ra and Ba due to export of sinking particulates, surpassing inputs from the continental margins. In contrast, deep waters have higher²²⁶Ra activities and Ba concentrations due to inputs from particle regeneration and sedimentary sources, with²²⁶Ra inputs primarily resulting from the decay of²³⁰Th in sediments. Further, dissolved²²⁶Ra and Ba exhibit a strong correlation along the GP15 section. To elucidate the drivers of the correlation, we used a water mass analysis, enabling us to quantify the influence of water mass mixing relative to non‐conservative processes. While a significant fraction of each element's distribution can be explained by conservative mixing, a considerable fraction cannot. The balance is driven using non‐conservative processes, such as sedimentary, rivers, or hydrothermal inputs, uptake and export by particles, and particle remineralization. Our study demonstrates the utility of²²⁶Ra and Ba as valuable biogeochemical tracers for understanding ocean processes, while shedding light on conservative and myriad non‐conservative processes that shape their respective distributions. 

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