Abstract Scarcity of iron and manganese limits the efficiency of the biological carbon pump over large areas of the Southern Ocean. The importance of hydrothermal vents as a source of these micronutrients to the euphotic zone of the Southern Ocean is debated. Here we present full depth profiles of dissolved and total dissolvable trace metals in the remote eastern Pacific sector of the Southern Ocean (55–60° S, 89.1° W), providing evidence of enrichment of iron and manganese at depths of 2000–4000 m. These enhanced micronutrient concentrations were co-located with 3He enrichment, an indicator of hydrothermal fluid originating from ocean ridges. Modelled water trajectories revealed the understudied South East Pacific Rise and the Pacific Antarctic Ridge as likely source regions. Additionally, the trajectories demonstrate pathways for these Southern Ocean hydrothermal ridge-derived trace metals to reach the Southern Ocean surface mixed layer within two decades, potentially supporting a regular supply of micronutrients to fuel Southern Ocean primary production.

The seasonal availability of light and micronutrients strongly regulates productivity in the Southern Ocean, restricting biological utilization of macronutrients and CO2 drawdown. Mineral dust flux is a key conduit for micronutrients to the Southern Ocean and a critical mediator of multimillennial-scale atmospheric CO2 oscillations. While the role of dust-borne iron (Fe) in Southern Ocean biogeochemistry has been examined in detail, manganese (Mn) availability is also emerging as a potential driver of past, present, and future Southern Ocean biogeochemistry. Here, we present results from fifteen bioassay experiments along a north-south transect in the undersampled eastern Pacific sub-Antarctic zone. In addition to widespread Fe limitation of phytoplankton photochemical efficiency, we found further responses following the addition of Mn at our southerly stations, supporting the importance of Fe-Mn co-limitation in the Southern Ocean. Moreover, addition of different Patagonian dusts resulted in enhanced photochemical efficiency with differential responses linked to source region dust characteristics in terms of relative Fe/Mn solubility. Changes in the relative magnitude of dust deposition, combined with source region mineralogy, could hence determine whether Fe or Mn limitation control Southern Ocean productivity under future as well as past climate states.

Supply of iron (Fe) to the surface ocean supports primary productivity, and while hydrothermal input of Fe to the deep ocean is known to be extensive it remains poorly constrained. Global estimates of hydrothermal Fe supply rely on using dissolved Fe (dFe) to excess He (xs3He) ratios to upscale fluxes, but observational constraints on dFe/xs3He may be sensitive to assumptions linked to sampling and interpolation. We examined the variability in dFe/xs3He using two methods of estimation, for four vent sites with different geochemistry along the Mid-Atlantic Ridge. At both Rainbow and TAG, the plume was sampled repeatedly and the range of dFe/xs3He was 4 to 63 and 4 to 87 nmol:fmol, respectively, primarily due to differences in plume age. To account for background xs3He and shifting plume position, we calibrated He values using contemporaneous dissolved Mn (dMn). Applying this approach more widely, we found dFe/xs3He ratios of 12, 4–8, 4–44, and 4–86 nmol fmol−1 for the Menez Gwen, Lucky Strike, Rainbow, and TAG hydrothermal vent sites, respectively. Differences in plume dFe/xs3He across sites were not simply related to the vent endmember Fe and He fluxes. Within 40 km of the vents, the dFe/xs3He ratios decreased to 3–38 nmol fmol−1, due to the precipitation and subsequent settling of particulates. The ratio of colloidal Fe to dFe was consistently higher (0.67–0.97) than the deep N. Atlantic (0.5) throughout both the TAG and Rainbow plumes, indicative of Fe exchange between dissolved and particulate phases. Our comparison of TAG and Rainbow shows there is a limit to the amount of hydrothermal Fe released from vents that can form colloids in the rising plume. Higher particle loading will enhance the longevity of the Rainbow hydrothermal plume within the deep ocean assuming particles undergo continual dissolution/disaggregation. Future studies examining the length of plume pathways required to escape the ridge valley will be important in determining Fe supply from slow spreading mid-ocean ridges to the deep ocean, along with the frequency of ultramafic sites such as Rainbow. Resolving the ridge valley bathymetry and accounting for variability in vent sources in global biogeochemical models will be key to further constraining the hydrothermal Fe flux.

Abstract. Supply of iron (Fe) to the surface ocean supports primary productivity and while hydrothermal input of Fe to the deep ocean is known to be extensive, it remains poorly constrained. Global estimates of hydrothermal Fe supply rely on using the dissolved Fe (dFe) to excess He (xs3He) ratios to upscale fluxes, but observational constraints on dFe / xs3He may be sensitive to assumptions linked to sampling and interpolation. We examined the variability in dFe / xs3He using two methods of estimation, for four vent sites with different geochemistry along the Mid-Atlantic Ridge. At both Rainbow and TAG, the plume was sampled repeatedly and the range of dFe / xs3He was 4 to 63 and 4 to 87 nmol/fmol, respectively, primarily due to differences in plume age. To account for background xs3He and shifting plume position, we calibrated He values using contemporaneous dissolved Mn (dMn). Applying this approach more widely, we found dFe / xs3He ratios of 12, 4–8, 4–44, 4–86 nmol/fmol for the Menez Gwen, Lucky Strike, Rainbow and TAG hydrothermal vent sites, respectively. Differences in plume dFe / xs3He across sites were not simply related to the vent end member Fe and He fluxes. Within 40 km of the vents, the dFe / xs3He ratios decreased to 3-38 nmol/fmol, due to the precipitation and subsequent settling of particulates. The ratio of colloidal Fe to dFe was consistently higher (0.67–0.97) than the deep N. Atlantic (0.5) throughout both the TAG and Rainbow plumes, indicative of Fe exchange between dissolved and particulate phases. Our comparison of TAG and Rainbow shows there is a limit to the amount of hydrothermal Fe released from vents that can form colloids in the rising plume. Higher particle loading will enhance the longevity of the Rainbow hydrothermal plume within the deep ocean assuming particles undergo continual dissolution/disaggregation. Future studies examining the length of plume pathways required to escape the ridge valley will be important in determining Fe supply from slow spreading mid-ocean ridges to the deep ocean, along with the frequency of ultramafic sites such as Rainbow. Resolving the ridge valley bathymetry and accounting for variability in vent sources in global biogeochemical models will be key to further constraining the hydrothermal Fe flux.

New dissolved aluminum (dAl) data from the 2017 GEOTRACES process study GApr08 along 22°N in the subtropical North Atlantic are presented. They show an east to west increase in dAl concentration in the surface waters. Simulation of these data with a 1D advection‐dust deposition revealed that, (a) advection and dust dissolution are equally important dAl sources, (b) scavenging plays a minor role compared to advection in dAl removal, and (c) in addition to dust dissolution, another dAl source is required at the westernmost stations to fully explain our observations. We attribute this additional source to the dissolution of erosion products delivered to the western subtropical North Atlantic by the Lesser Antilles. For waters deeper than ∼200–300 m, an optimum multi‐parameter analysis allowed to separate the component of the dAl signal derived from water mass transport from its biogeochemical component. This revealed, (a) a major role played by water mass transport, (b) a net dAl removal between 200 and 800 m, attributed to scavenging at the subtropical North Atlantic scale, and (c) internal dAl inputs between 800 m and the seafloor, attributed to reversible scavenging. While the dAl oceanic distribution is usually considered to be dominated by the atmospheric dust input and removal by particle scavenging, this study highlights the important role played by advection, and the need to explicitly take this into account in order to quantitatively reveal the impact of external sources and dissolved‐particulate interactions on the Al cycle in the North Atlantic Ocean.

We report the distributions and stoichiometry of dissolved zinc (dZn) and cobalt (dCo) in sub-tropical and sub-Antarctic waters of the south-eastern Atlantic Ocean during austral spring 2010 and summer 2011/2012. In sub-tropical surface waters, mixed-layer dZn and dCo concentrations during early spring were 1.60 ± 2.58 nM and 30 ± 11 pM, respectively, compared with summer values of 0.14 ± 0.08 nM and 24 ± 6 pM. The elevated spring dZn concentrations resulted from an apparent offshore transport of elevated dZn at depths between 20–55 m, derived from the Agulhas Bank. In contrast, open-ocean sub-Antarctic surface waters displayed largely consistent inter-seasonal mixed-layer dZn and dCo concentrations of 0.10 ± 0.07 nM and 11 ± 5 pM, respectively. Trace metal stoichiometry, calculated from concentration inventories, suggests a greater overall removal for dZn relative to dCo in the upper water column of the south-eastern Atlantic, with inter-seasonally decreasing dZn / dCo inventory ratios of 19–5 and 13–7 mol mol−1 for sub-tropical surface water and sub-Antarctic surface water, respectively. In this paper, we investigate how the seasonal influences of external input and phytoplankton succession may relate to the distribution of dZn and dCo and variation in dZn / dCo stoichiometry across these two distinct ecological regimes in the south-eastern Atlantic.

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 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=1.8±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 = 1.0–1.7 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 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.

Iron (Fe) is an essential nutrient for primary production and is known to limit the efficiency of the biological carbon pump over large areas of the ocean. As a non-conservative element with a residence time on the order of decades to centuries in the deep ocean, the distribution of dissolved Fe (dFe; <0.2 µm) in seawater is closely coupled to its sources. Early studies suggested that the dFe supplied from hydrothermal vents is precipitated/scavenged and sedimented close to vent sites. However, it is now known that a significant fraction of dFe supplied from hydrothermal vents is stabilised through organic complexation and/or formation of inorganic colloids and transported 1000’s km into the ocean interior. Hydrothermal venting is estimated to supply 4 ± 1 Gmol dFe yr -1 to the deep ocean, yet the proportion of this dFe that reaches the euphotic zone and sustains primary production remains unclear. As part of the Carbon Uptake and Seasonal Traits in Antarctic Remineralisation Depth (https://roses.ac.uk/custard/) programme, we present results from a north-south transect (89 o W, 55 o S to 89 o W, 60 o S) comprised of 7 full ocean depth profiles of the poorly studied southeast Pacific Ocean. We observed a significant increase in the dFe concentration ( ≈ 0.7 nM, background concentrations ≈ 0.4 nM) on a shoaling density surface at intermediate depths (2000-4000 m). We combine our observations of dFe with historic 3 He profiles to make the case for a hydrothermal Fe source (Fig. 1), despite the considerable distance of our study area ( ≈ 1500 km) from ridge systems. We further interpret soluble (<0.02 µm) and total dissolvable

We believe the reviewers present extremely valid comments, particularly on the 'interpretation of data', that has led us to reconsider how we approach certain aspects of the data.Specifically, we acknowledge and agree with the suggestion that the use of slopes of regression to infer biological uptake and remineralisation is flawed by the varying influences of other sources on the correlation, most notably water mass C1

The size partitioning of dissolved trace metals is an important factor for determining reactivity and bioavailability of metals in marine environments. This, alongside the advent of more routine shipboard ultrafiltration procedures, has led to increased attention in determining the colloidal phase of metals such as Fe in seawater. While clean and efficient filtration, prompt acidification, and proper storage have long been tenets of trace metal biogeochemistry, few studies aim to quantify the kinetics of colloidal exchange and metal adsorption to bottle walls during storage and acidification. This study evaluates the effect of storage conditions on colloidal size partitioning, the kinetics of colloid exchange over time, and the timescale of bottle wall adsorption and desorption for dissolved Fe, Cu, Ni, Zn, Cd, Pb, Mn and Co. We report that preservation of dissolved size partitioning is possible only for Fe and only under frozen conditions. All metals except Mn and Cd show regeneration of the colloidal phase following its removal in as short as 14 h, validating the importance of prompt ultrafiltration. Adsorption of metals to bottle walls is a well-known sampling artifact often cited for Fe and assumed to be potentially significant for other metals as well. However, only Fe and Co showed significant proclivity to adsorption onto low density polyethylene bottle walls, sorbing a maximum of 91 and 72% over 40 months, respectively. After 20 weeks of acidification neither Fe nor Co desorbed to their original concentrations, leading to an acidified storage recommendation of 30 weeks prior to analyses following storage of unacidified samples for long periods of time. This study provides empirical recommendations for colloidal and dissolved trace metal methodology while also paving the way for much-needed future methods testing.

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 degrees 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 similar to 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.

The authors of this manuscript would like to thank the reviewers for their wellconsidered review and advice on preparing our manuscript for publication in Biogeosciences. We believe the reviewers present extremely valid comments, particularly on the ‘interpretation of data’, that has led us to reconsider how we approach certain aspects of the data. Specifically, we acknowledge and agree with the suggestion that the use of slopes of regression to infer biological uptake and remineralisation is flawed by the varying influences of other sources on the correlation, most notably water mass

Key Points Size‐fractionation reveals that colloidal iron is more important than soluble iron for distribution of dissolved iron in North Atlantic Colloidal iron is the predominantly active species at key supply and removal processes of the dissolved iron cycle Global comparison suggests that the colloidal iron fraction in mesopelagic zone is determined by the local lithogenic contribution

The biogeochemical cycling of dissolved zinc (dZn) was investigated in the Western Arctic along the U.S. GEOTRACES GN01 section. Vertical profiles of dZn in the Arctic are strikingly different than the classic “nutrient‐type” profile commonly seen in the Atlantic and Pacific Oceans, instead exhibiting higher surface concentrations (~1.1 nmol/kg), a shallow subsurface absolute maximum (~4–6 nmol/kg) at 200 m coincident with a macronutrient maximum, and low deep water concentrations (~1.3 nmol/kg) that are homogeneous (sp.) with depth. In contrast to other ocean basins, typical inputs such as rivers, atmospheric inputs, and especially deep remineralization are insignificant in the Arctic. Instead, we demonstrate that dZn distributions in the Arctic are controlled primarily by (1) shelf fluxes following the sediment remineralization of high Zn:C and Zn:Si cells and the seaward advection of those fluxes and (2) mixing of dZn from source waters such as the Atlantic and Pacific Oceans rather than vertical biological regeneration of dZn. This results in both the unique profile shapes and the largely decoupled relationship between dZn and Si found in the Arctic. We found a weak dZn:Si regression in the full water column (0.077 nmol/μmol, r2 = 0.58) that is higher than the global slope (0.059 nmol/μmol, r2 = 0.94) because of the shelf‐derived halocline dZn enrichments. We hypothesize that the decoupling of Zn:Si in Western Arctic deep waters results primarily from a past ventilation event with unique preformed Zn:Si stoichiometries.

The GEOTRACES Intermediate Data Product 2017 (IDP2017) is the second publicly available data product of the international GEOTRACES programme, and contains data measured and quality controlled before the end of 2016. The IDP2017 includes data from the Atlantic, Pacific, Arctic, Southern and Indian oceans, with about twice the data volume of the previous IDP2014. For the first time, the IDP2017 contains data for a large suite of biogeochemical parameters as well as aerosol and rain data characterising atmospheric trace element and isotope (TEI) sources. The TEI data in the IDP2017 are quality controlled by careful assessment of intercalibration results and multi-laboratory data comparisons at crossover stations. The IDP2017 consists of two parts: (1) a compilation of digital data for more than 450 TEIs as well as standard hydrographic parameters, and (2) the eGEOTRACES Electronic Atlas providing an on-line atlas that includes more than 590 section plots and 130 animated 3D scenes. The digital data are provided in several formats, including ASCII, Excel spreadsheet, netCDF, and Ocean Data View collection. Users can download the full data packages or make their own custom selections with a new on-line data extraction service. In addition to the actual data values, the IDP2017 also contains data quality flags and 1-σ data error values where available. Quality flags and error values are useful for data filtering and for statistical analysis. Metadata about data originators, analytical methods and original publications related to the data are linked in an easily accessible way. The eGEOTRACES Electronic Atlas is the visual representation of the IDP2017 as section plots and rotating 3D scenes. The basin-wide 3D scenes combine data from many cruises and provide quick overviews of large-scale tracer distributions. These 3D scenes provide geographical and bathymetric context that is crucial for the interpretation and assessment of tracer plumes near ocean margins or along ridges. The IDP2017 is the result of a truly international effort involving 326 researchers from 25 countries. This publication provides the critical reference for unpublished data, as well as for studies that make use of a large cross-section of data from the IDP2017.This article is part of a special issue entitled: "Cycles of trace elements and isotopes in the ocean – GEOTRACES and beyond" - edited by Tim M. Conway, Tristan Horner, Yves Plancherel, and Aridane G. González.

In the ocean, dissolved cobalt is affected by both nutrient cycling and scavenging onto manganese oxides. The latter process concentrates Co in pelagic sediments, resulting in a small deep water inventory. While the flux of scavenged cobalt to sediments appears steady on timescales>100,000years, its residence time in the water column is short, approximately 130years. Using results from recent GEOTRACES expeditions, we show net removal of dissolved Co from the deep ocean on the order of 0.043pMyear−1, which corresponds to a turnover time of 980years. Scavenging in deep ocean water masses is too slow to match cobalt accumulation rates in marine sediments, requiring most of the scavenging flux to derive from the mesopelagic ocean (<1500m depth) where nutrient cycling is active. Based on differences between the Co:P stoichiometry in particles sinking from the euphotic zone and dissolved Co:P remineralization ratios, we calculate areal scavenging rates in the North Atlantic and South Pacific basins on the order of 1.5 and 0.7μmol m−2year−1, respectively, which agree with long-term accumulation rates in Atlantic and Pacific sediments. In both basins, over 50% of the scavenged flux of cobalt occurs in the upper 500m, resulting in decadal turnover times in the mesopelagic. An assessment of sources suggests that the marine cobalt cycle is approximately in balance, but that this inventory may be sensitive to long term trends in the intensity of oxygen minimum zones, which account for ~25% of the annual cobalt source to the modern oceans.

Cobalt (Co) and iron (Fe) are essential for phytoplankton nutrition, and as such constitute a vital link in the marine biological carbon pump. Atmospheric deposition is an important, and in some places the dominant, source of trace elements (TEs) to the global ocean. Dissolved cobalt (dCo) and iron (dFe) were determined along an Atlantic Meridional Transect (AMT-19; Oct/Nov 2009) between 50 degrees N and 40 degrees S in the upper 150 m in order to investigate the behaviour and distribution of these two essential, bioactive TEs. During AMT-19, large differences in the distributions of dCo and dFe were observed. In the North Atlantic gyre provinces, extremely low mixed layer dCo concentrations (23 +/- 9 pM) were observed, which contrasts with the relatively high mixed layer dFe concentrations (up to 1.0 nM) coincident with the band of highest atmospheric deposition (similar to 5-30 degrees N). In the South Atlantic gyre, the opposite trend was observed, with relatively high dCo (55 +/- 18 pM) observed throughout the water column, but low dFe concentrations (0.29 +/- 0.08 nM). Given that annual dust supply is an order of magnitude greater in the North than the South Atlantic, the dCo distribution was somewhat unexpected. However, the distribution of dCo shows similarities with the distribution of phosphate (PO43-) in the euphotic zone of the Atlantic Ocean, where the North Atlantic gyre is characterised by chronically low PO4, and higher concentrations are observed in the South Atlantic gyre (Mather et al., 2008), suggesting the potential for a similar biological control of dCo distributions. Inverse correlations between dCo and Prochlorococcus abundance in the North Atlantic gyre provinces, combined with extremely low dCo where nitrogen fixation rates were highest (similar to 20-28 degrees N), suggests the dominance of biological controls on dCo distributions. The conr trasting dCo and dFe distributions in the North and South Atlantic gyres provides insights into the differences between the dominant controls on the distribution of these two bioactive trace metals in the central Atlantic Ocean. (c) 2016 Elsevier Ltd. All rights reserved.

The GEOTRACES Intermediate Data Product 2014 (IDP2014) is the first publicly available data product of the international GEOTRACES programme, and contains data measured and quality controlled before the end of 2013. It consists of two parts: (1) a compilation of digital data for more than 200 trace elements and isotopes (TEls) as well as classical hydrographic parameters, and (2) the eGEOTRACES Electronic Atlas providing a strongly inter-linked on-line atlas including more than 300 section plots and 90 animated 3D scenes. The IDP2014 covers the Atlantic, Arctic, and Indian oceans, exhibiting highest data density in the Atlantic. The TEI data in the IDP2014 are quality controlled by careful assessment of intercalibration results and multi-laboratory data comparisons at cross-over stations. The digital data are provided in several formats, including ASCII spreadsheet, Excel spreadsheet, netCDF, and Ocean Data View collection. In addition to the actual data values the IDP2014 also contains data quality flags and 1-sigma data error values where available. Quality flags and error values are useful for data filtering. Metadata about data originators, analytical methods and original publications related to the data are linked to the data in an easily accessible way. The eGEOTRACES Electronic Atlas is the visual representation of the IDP2014 data providing section plots and a new kind of animated 3D scenes. The basin-wide 3D scenes allow for viewing of data from many cruises at the same time, thereby providing quick overviews of large-scale tracer distributions. In addition, the 3D scenes provide geographical and bathymetric context that is crucial for the interpretation and assessment of observed tracer plumes, as well as for making inferences about controlling processes. (C) 2015 The Authors. Published by Elsevier B.V.

The biogeochemical cycle of zinc (Zn) in the South Atlantic, at 40 degrees S, was investigated as part of the UK GEOTRACES program. To date there is little understanding of the supply of Zn, an essential requirement for phytoplankton growth, to this highly productive region. Vertical Zn profiles displayed nutrient-like distributions with distinct gradients associated with the water masses present. Surface Zn concentrations are among the lowest reported for the world's oceans (< 50 pM). A strong Zn-Si linear relationship was observed (Zn (nM)=0.065 Si (M), r(2)=0.97, n=460). Our results suggest that the use of a global Zn-Si relationship would lead to an underestimation of dissolved Zn in deeper waters of the South Atlantic. By utilizing Si* and a new tracer Zn* our data indicate that the preferential removal of Zn in the Southern Ocean prevented a direct return path for dissolved Zn to the surface waters of the South Atlantic at 40 degrees S and potentially the thermocline waters of the South Atlantic subtropical gyre. The importance of Zn for phytoplankton growth was evaluated using the Zn-soluble reactive phosphorus (SRP) relationship. We hypothesize that the low Zn concentrations in the South Atlantic may select for phytoplankton cells with a lower Zn requirement. In addition, a much deeper kink at similar to 500m in the Zn:SRP ratio was observed compared to other oceanic regions.Key Points Dissolved zinc biogeochemical cycle investigated in the South Atlantic Ocean