Search

Hydrothermal vent sites found along mid-ocean ridges are sources of numerous reduced chemical species and trace elements. To establish dissolved iron (II) (dFe(II)) variability along the Mid Atlantic Ridge (between 39.5°N and 26°N), dFe(II) concentrations were measured above six hydrothermal vent sites, as well as at stations with no active hydrothermal activity. The dFe(II) concentrations ranged from 0.00 to 0.12 nmol L -1 (detection limit = 0.02 ± 0.02 nmol L -1 ) in non-hydrothermally affected regions to values as high as 12.8 nmol L -1 within hydrothermal plumes. Iron (II) in seawater is oxidised over a period of minutes to hours, which is on average two times faster than the time required to collect the sample from the deep ocean and its analysis in the onboard laboratory. A multiparametric equation was used to estimate the original dFe(II) concentration in the deep ocean. The in-situ temperature, pH, salinity and delay between sample collection and its analysis were considered. The results showed that dFe(II) plays a more significant role in the iron pool than previously accounted for, constituting a fraction >20 % of the dissolved iron pool, in contrast to <10 % of the iron pool formerly reported. This discrepancy is caused by Fe(II) loss during sampling when between 35 and 90 % of the dFe(II) gets oxidised. In-situ dFe(II) concentrations are therefore significantly higher than values reported in sedimentary and hydrothermal settings where Fe is added to the ocean in its reduced form. Consequently, the high dynamism of dFe(II) in hydrothermal environments masks the magnitude of dFe(II) sourced within the deep ocean., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.)

The international GEOTRACES program was developed to enhance knowledge about the distribution of trace elements and their isotopes (TEIs) in the ocean and to reduce the uncertainty about their sources, sinks, and internal cycling. Recognizing the importance of intercalibration from the outset, GEOTRACES implemented intercalibration efforts early in the program, and consensus materials were generated that included the full range of TEIs dissolved in seawater, in suspended particles, and from aerosols. The GEOTRACES section cruises include "crossover station(s)" that are occupied by two or more sections and whereby all aspects of sample collection, preservation, and processing can be compared and intercalibrated. Once data-sets are generated, an international intercalibration committee reviews intercalibration reports and works with the community to address issues and provide intercalibrated data for intermediate data products. This process has resulted in a highly cooperative community that shares advances in protocols to strengthen capacity building and GEOTRACES outcomes, including an unprecedented oceanic atlas of TEIs, with data quality that is state-of-the-art. This article outlines the development and implementation of the successful GEOTRACES intercalibration process. [ABSTRACT FROM AUTHOR]

Continental shelves and shelf seas play a central role in the global carbon cycle. However, their importance with respect to trace element and isotope (TEI) inputs to ocean basins is less well understood. Here, we present major findings on shelf TEI biogeochemistry from the GEOTRACES programme as well as a proof of concept for a new method to estimate shelf TEI fluxes. The case studies focus on advances in our understanding of TEI cycling in the Arctic, transformations within a major river estuary (Amazon), shelf sediment micronutrient fluxes and basin-scale estimates of submarine groundwater discharge. The proposed shelf flux tracer is 228-radium (T1/2 = 5.75 yr), which is continuously supplied to the shelf from coastal aquifers, sediment porewater exchange and rivers. Model-derived shelf 228Ra fluxes are combined with TEI/ 228Ra ratios to quantify ocean TEI fluxes from the western North Atlantic margin. The results from this new approach agree well with previous estimates for shelf Co, Fe, Mn and Zn inputs and exceed published estimates of atmospheric deposition by factors of approximately 3-23. Lastly, recommendations are made for additional GEOTRACES process studies and coastal margin-focused section cruises that will help refine the model and provide better insight on the mechanisms driving shelf-derived TEI fluxes to the ocean.This article is part of the themed issue 'Biological and climatic impacts of ocean trace element chemistry'.

Trace elements (TEs) play important roles as micronutrients in modulating marine productivity in the global ocean. The South Atlantic around 40 ∘ S is a prominent region of high productivity and a transition zone between the nitrate-depleted subtropical gyre and the iron-limited Southern Ocean. However, the sources and fluxes of trace elements to this region remain unclear. In this study, the distribution of the naturally occurring radioisotope 228 Ra in the water column of the South Atlantic (Cape Basin and Argentine Basin) has been investigated along a 40 ∘ S zonal transect to estimate ocean mixing and trace element supply to the surface ocean. Ra-228 profiles have been used to determine the horizontal and vertical mixing rates in the near-surface open ocean. In the Argentine Basin, horizontal mixing from the continental shelf to the open ocean shows an eddy diffusion of Kx=1.8±1.4 (10 6 cm 2 s -1) and an integrated advection velocity w=0.6±0.3 cm s -1. In the Cape Basin, horizontal mixing is Kx=2.7±0.8 (10 7 cm 2 s -1) and vertical mixing Kz = 1.0–1.7 cm 2 s -1 in the upper 600 m layer. Three different approaches (228 Ra diffusion, 228 Ra advection, and 228Ra/TE ratio) have been applied to estimate the dissolved trace element fluxes from the shelf to the open ocean. These approaches bracket the possible range of off-shelf fluxes from the Argentine Basin margin to be 4–21 (×103) nmol Co m -2 d -1 , 8–19 (×104) nmol Fe m -2 d -1 and 2.7–6.3 (×104) nmol Zn m -2 d -1. Off-shelf fluxes from the Cape Basin margin are 4.3–6.2 (×103) nmol Co m -2 d -1 , 1.2–3.1 (×104) nmol Fe m -2 d -1 , and 0.9–1.2 (×104) nmol Zn m -2 d -1. On average, at 40 ∘ S in the Atlantic, vertical mixing supplies 0.1–1.2 nmol Co m -2 d -1 , 6–9 nmol Fe m -2 d -1 , and 5–7 nmol Zn m -2 d -1 to the euphotic zone. Compared with atmospheric dust and continental shelf inputs, vertical mixing is a more important source for supplying dissolved trace elements to the surface 40 ∘ S Atlantic transect. It is insufficient, however, to provide the trace elements removed by biological uptake, particularly for Fe. Other inputs (e.g. particulate or from winter deep mixing) are required to balance the trace element budgets in this region. [ABSTRACT FROM AUTHOR]

Trace elements play important roles as micronutrients in modulating marine productivity in the global ocean. The South Atlantic around 40°S is a prominent region of high productivity and a transition zone between the nitrate-depleted Subtropical Gyre and the iron-limited Southern Ocean. However, the sources and fluxes of trace elements to this region remain unclear. In this study, the distribution of the naturally occurring radioisotope 228Ra in the water column of the South Atlantic (Cape Basin and Argentine Basin) has been investigated along a 40°S zonal transect to estimate ocean mixing and trace element supply to the surface ocean. Ra-228 profiles have been used to determine the horizontal and vertical mixing rates in the near-surface open ocean. In the Argentine Basin, horizontal mixing from the continental shelf to the open ocean shows an eddy diffusion of Kx = 1.7 ± 1.4 (106 cm² s-1) and an integrated advection velocity w = 0.6 ± 0.3 cm s-1. In the Cape Basin, horizontal mixing is Kx = 2.7 ± 0.8 (107 cm² s-1) and vertical mixing Kz = 1.0 - 1.5 cm² s-1 in the upper 600 m layer. Three different approaches (228Ra-diffusion, 228Ra-advection and 228Ra/TE-ratio) have been applied to estimate the dissolved trace-element fluxes from shelf to open ocean. These approaches bracket the possible range of off-shelf fluxes from the Argentine margin to be: 3.8 - 22 (x10³) nmol Co m-2 d-1, 7.9 - 20 (x104) nmol Fe m-2 d-1 and 2.7 - 6.5 (x104) nmol Zn m-2 d-1. Off-shelf fluxes from the Cape margin are: 4.3 - 6.2 (x10³) nmol Co m-2 d-1, 1.2 - 3.1 (x104) nmol Fe m-2 d-1 and 0.9 - 1.2 (x104) nmol Zn m-2 d-1. On average, at 40°S in the Atlantic, vertical mixing supplies 0.4 - 1.2 nmol Co m-2 d-1, 3.6 - 11 nmol Fe m-2 d-1, and 13 - 16 nmol Zn m-2 d-1 to the euphotic zone. Compared with atmospheric dust and continental shelf inputs, vertical mixing is a more important source for supplying dissolved trace elements to the surface 40°S Atlantic. It is insufficient, however, to provide the trace elements removed by biological uptake. Other inputs (e.g. particulate, or from [ABSTRACT FROM AUTHOR]

This paper overviews the evolution of suitable analytical approaches for the determination of dissolved iron in seawater. The focus is on sampling and sample treatment, detection methods and quality assurance of the data. Iron is a vital trace element for the growth of marine organisms and is the limiting micronutrient for primary production in many parts of the world's oceans. The concentration of dissolved iron in seawater therefore influences the past and present day global carbon cycle and consequently Earth's climate. Hence it is important to understand the marine biogeochemistry of iron and quantify the spatial and temporal distribution of the element. In order to do this, it is essential that robust and validated methods with appropriate detection limits, precision and accuracy are available for the determination of iron species in seawater. [ABSTRACT FROM AUTHOR]

The concentrations of Cd, Cr, Cu, Fe, Mn, Ni, Pb and Zn were measured in several soft-tissue types of the Antarctic soft-shelled clam, Laternula elliptica, which had been collected from Rothera Research Station, Adelaide Island, Antarctic Peninsula. Concentrations of Mn, Ni, Cr and Pb were significantly higher in the kidney than in any other soft tissue and highest concentrations of Cu were observed in the digestive gland. In general, the total tissue concentrations of heavy metals in L. elliptica were considered to be at baseline levels, except for Cu in organisms near the end of the runway. Copper concentrations were an order of magnitude greater (357 µg/g dry weight) than baseline levels, suggesting anthropogenic contamination or an unidentified natural source. However, there was no indication of anthropogenic metal contamination occurring close to the sewage outfall at Rothera, which is a significant metal source. The results indicate that L. elliptica is a useful long-term biomonitor of heavy metal contamination in Antarctic coastal waters. [ABSTRACT FROM AUTHOR]

This study presents a water mass analysis along the JC150 section in the subtropical North Atlantic, based on hydrographic and nutrient data, by combining an extended optimum multiparameter analysis (OMPA) with a Lagrangian particle tracking experiment (LPTE). This combination, which was proposed for the first time, aided in better constraining the OMPA end-member choice and providing information about their trajectories. It also enabled tracing the water mass origins in surface layers, which cannot be achieved with an OMPA. The surface layers were occupied by a shallow type of Eastern South Atlantic Central Water (ESACW) with traces of the Amazon plume in the west. Western North Atlantic Central Water dominates from 100 to 500 m, while the 13 °C-ESACW contribution occurs marginally deeper (500–900 m). At approximately 700 m, Antarctic Intermediate Water (AAIW) dominates the west of the Mid-Atlantic Ridge (MAR), while Mediterranean Water dominates the east with a small but non-negligible contribution down to 3500 m. Below AAIW, Upper Circumpolar Deep Water (UCDW) is observed throughout section (900–1250 m). Labrador Sea Water (LSW) is found centered at 1500 m, where the LPTE highlights an eastern LSW route from the eastern North Atlantic to the eastern subtropical Atlantic, which was not previously reported. North East Atlantic Deep Water (encompassing a contribution of Iceland-Scotland Overflow Water) is centered at ~2500 m, while North West Atlantic Bottom Water (NWABW, encompassing a contribution of Denmark Strait Overflow Water) is principally localized in the west of the MAR in the range of 3500–5000 m. NWABW is also present in significant proportions (>25%) in the east of the MAR, suggesting a crossing of the MAR possibly through the Kane fracture zone. This feature has not been investigated so far. Finally, Antarctic Bottom Water is present in deep waters throughout the section, mainly in the west of the MAR. Source waters have been characterized from GEOTRACES sections, which enables estimations of trace elements and isotope transport within water masses in the subtropical North Atlantic. Image 1 • Optimum multiparameter analysis combined with a Lagrangian particle tracking experiment. • Impact of Amazon River plume identified as north as 22°N. • Mediterranean Water impact on North Atlantic Deep Water salinity as deep as 3500 m. • Un-previously described Labrador Sea Water route in the eastern North Atlantic. • North West Atlantic Bottom Water transport across the Mid-Atlantic Ridge. [ABSTRACT FROM AUTHOR]