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Controls on distributions of aluminium, manganese and cobalt in the South Atlantic Ocean along GEOTRACES transect GA10

Controls on distributions of aluminium, manganese and cobalt in the South Atlantic Ocean along GEOTRACES transect GA10
Controls on distributions of aluminium, manganese and cobalt in the South Atlantic Ocean along GEOTRACES transect GA10
Trace metals (TMs) manganese (Mn), cobalt (Co), and aluminium (Al) have important geochemical and biological roles in the ocean. Here, we present full depth profiles of dissolved (d) and particulate Al, Mn, and Co along the latitude of 40 °S in the South Atlantic Ocean from the GEOTRACES GA10 cruises that operated in austral spring 2010 and summer 2011. The region is characterized by enhanced primary productivity and forms a key transition zone between the Southern Ocean and South Atlantic Subtropical Gyre. The mean concentrations of dAl, dCo, and dMn (±standard deviation) were 3.36 ± 2.65 nmol kg−1, 35.3 ± 17.6 pmol kg−1, and 0.624 ± 1.08 nmol kg−1, respectively. Their distributions in surface waters were determined by external sources and complex internal biogeochemical processes. Specifically, surface ocean dCo was controlled by the interplay between phytoplankton uptake, remineralization and external inputs; dMn was likely determined by the formation and photoreduction of Mn-oxides; and dAl was supplied by atmospheric deposition and removed by scavenging onto particles. Fluvial and sedimentary inputs near the Rio de La Plata estuary and benthic sources from the Agulhas Bank resulted in elevated dTM concentrations in near-shore surface waters. These externally sourced dTMs were effectively delivered to the open ocean by offshore diffusion and/or advection, and potentially facilitated enhanced primary productivity along the transect.
The distributions of dTMs at depth were predominantly controlled by the mixing of North Atlantic Deep Water (NADW) and waters of Antarctic origin (e.g., Upper Circumpolar Water (UCDW) and Antarctic Bottom Water (AABW)). The calculated endmember concentrations of dAl and dCo in NADW showed minor decreases in the SASTG following north–south transport, suggesting removal rates of 0.064 nM/year and 0.035–0.075 pM/year, respectively. The endmember concentration of dCo in AABW was maintained at ∼30 pmol kg−1 without evidence for scavenging removal in the Southern Ocean and SASTG (time frame >400 years). The concentrations of dMn in NADW and AABW were between 0.1 and 0.16 nmol kg−1, and any elevated dMn concentrations were ascribed to local external inputs (e.g., from sediments in the Argentine Basin and hydrothermal activity near the Mid-Atlantic Ridge). Hence, four controlling factors (sources, internal cycling, water mass mixing and time) need to be considered when assessing TM distributions in the global ocean, even for TMs that are vulnerable to scavenging removal processes. Because the deep waters formed in high latitude oceans are crucial components of the global thermohaline overturning system, any processes (e.g., glacier melting, upwelling and sinking, and biological activity) that impact the preformed dTM concentrations in high latitude oceans will determine the downstream dTM distributions. Therefore, the sources and sinks of TMs and associated biological activity in high latitude oceans could engender basin to global scale impacts on seawater distributions of Al, Co, and Mn and their stoichiometric relationships with macronutrients, and the global biogeochemical cycles of these scavenged-type TMs.
0016-7037
177 - 196
Chen, Xue-Gang
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Milne, Angela
21ceb6ee-f9ba-43b2-a273-591caa9c8818
Klar, Jessica
2a95465e-3c3e-475f-a881-fd76f5819f73
Gledhill, Martha
3393b886-d88e-4417-b399-ae2a01443a19
Lohan, Maeve
6ca10597-2d0f-40e8-8e4f-7619dfac5088
Hsieh, Yu-Te
e61cbc9a-d3a5-419a-8c4d-f0f0aed1fa5c
Henderson, Gideon
f3effad0-d3f6-4cc1-ad87-558acc5c95a3
Achterberg, Eric
da742b45-3cf2-4ab4-8a51-1da00254c686
Woodward, E. Malcolm S.
3a11b7bf-b110-448a-b1ee-ae1ce7d0fef5
Chen, Xue-Gang
b65dfe28-0cdd-4607-8298-2d6fe6570cee
Milne, Angela
21ceb6ee-f9ba-43b2-a273-591caa9c8818
Klar, Jessica
2a95465e-3c3e-475f-a881-fd76f5819f73
Gledhill, Martha
3393b886-d88e-4417-b399-ae2a01443a19
Lohan, Maeve
6ca10597-2d0f-40e8-8e4f-7619dfac5088
Hsieh, Yu-Te
e61cbc9a-d3a5-419a-8c4d-f0f0aed1fa5c
Henderson, Gideon
f3effad0-d3f6-4cc1-ad87-558acc5c95a3
Achterberg, Eric
da742b45-3cf2-4ab4-8a51-1da00254c686
Woodward, E. Malcolm S.
3a11b7bf-b110-448a-b1ee-ae1ce7d0fef5

Chen, Xue-Gang, Milne, Angela, Klar, Jessica, Gledhill, Martha, Lohan, Maeve, Hsieh, Yu-Te, Henderson, Gideon, Achterberg, Eric and Woodward, E. Malcolm S. (2024) Controls on distributions of aluminium, manganese and cobalt in the South Atlantic Ocean along GEOTRACES transect GA10. Geochimica et Cosmochimica Acta, 373, 177 - 196. (doi:10.1016/j.gca.2024.03.019).

Record type: Article

Abstract

Trace metals (TMs) manganese (Mn), cobalt (Co), and aluminium (Al) have important geochemical and biological roles in the ocean. Here, we present full depth profiles of dissolved (d) and particulate Al, Mn, and Co along the latitude of 40 °S in the South Atlantic Ocean from the GEOTRACES GA10 cruises that operated in austral spring 2010 and summer 2011. The region is characterized by enhanced primary productivity and forms a key transition zone between the Southern Ocean and South Atlantic Subtropical Gyre. The mean concentrations of dAl, dCo, and dMn (±standard deviation) were 3.36 ± 2.65 nmol kg−1, 35.3 ± 17.6 pmol kg−1, and 0.624 ± 1.08 nmol kg−1, respectively. Their distributions in surface waters were determined by external sources and complex internal biogeochemical processes. Specifically, surface ocean dCo was controlled by the interplay between phytoplankton uptake, remineralization and external inputs; dMn was likely determined by the formation and photoreduction of Mn-oxides; and dAl was supplied by atmospheric deposition and removed by scavenging onto particles. Fluvial and sedimentary inputs near the Rio de La Plata estuary and benthic sources from the Agulhas Bank resulted in elevated dTM concentrations in near-shore surface waters. These externally sourced dTMs were effectively delivered to the open ocean by offshore diffusion and/or advection, and potentially facilitated enhanced primary productivity along the transect.
The distributions of dTMs at depth were predominantly controlled by the mixing of North Atlantic Deep Water (NADW) and waters of Antarctic origin (e.g., Upper Circumpolar Water (UCDW) and Antarctic Bottom Water (AABW)). The calculated endmember concentrations of dAl and dCo in NADW showed minor decreases in the SASTG following north–south transport, suggesting removal rates of 0.064 nM/year and 0.035–0.075 pM/year, respectively. The endmember concentration of dCo in AABW was maintained at ∼30 pmol kg−1 without evidence for scavenging removal in the Southern Ocean and SASTG (time frame >400 years). The concentrations of dMn in NADW and AABW were between 0.1 and 0.16 nmol kg−1, and any elevated dMn concentrations were ascribed to local external inputs (e.g., from sediments in the Argentine Basin and hydrothermal activity near the Mid-Atlantic Ridge). Hence, four controlling factors (sources, internal cycling, water mass mixing and time) need to be considered when assessing TM distributions in the global ocean, even for TMs that are vulnerable to scavenging removal processes. Because the deep waters formed in high latitude oceans are crucial components of the global thermohaline overturning system, any processes (e.g., glacier melting, upwelling and sinking, and biological activity) that impact the preformed dTM concentrations in high latitude oceans will determine the downstream dTM distributions. Therefore, the sources and sinks of TMs and associated biological activity in high latitude oceans could engender basin to global scale impacts on seawater distributions of Al, Co, and Mn and their stoichiometric relationships with macronutrients, and the global biogeochemical cycles of these scavenged-type TMs.

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Accepted/In Press date: 21 March 2024
e-pub ahead of print date: 28 March 2024
Published date: 9 April 2024

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Local EPrints ID: 502332
URI: http://eprints.soton.ac.uk/id/eprint/502332
ISSN: 0016-7037
PURE UUID: eeda289f-74e7-4882-b504-51455830a9b4
ORCID for Maeve Lohan: ORCID iD orcid.org/0000-0002-5340-3108

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Date deposited: 23 Jun 2025 16:36
Last modified: 22 Aug 2025 02:08

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Contributors

Author: Xue-Gang Chen
Author: Angela Milne
Author: Jessica Klar
Author: Martha Gledhill
Author: Maeve Lohan ORCID iD
Author: Yu-Te Hsieh
Author: Gideon Henderson
Author: Eric Achterberg
Author: E. Malcolm S. Woodward

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