Physical and remineralization processes govern the cobalt distribution in the deep western Atlantic Ocean

International audienceThe distributions of the bio-essential trace element dissolved cobalt (DCo) and the apparent particulate Co (PCo) are presented along the GEOTRACES-A02 deep section from 64° N to 50° S in the western Atlantic Ocean (longest section of international GEOTRACES marine environment program). PCo was determined as the difference between total cobalt (T Co, unfiltered samples) and DCo. DCo concentrations ranged from 14.7pM to 94.3 pM, and PCo concentrations from undetectable values to 18.8 pM. The lowest DCo concentrations were observed in the subtropical domains, and the highest in the low-oxygenated Atlantic Central Waters (ACW), which appears to be the major reservoir of DCo in the western Atlantic. In the Antarctic Bottom Waters, the enrichment in DCo with aging of the water mass can be related to suspension and redissolution of bottom sediments a well as diffusion of DCo from abyssal sediments. Mixing and dilution of deep water masses, rather than scavenging of DCo onto settling particles, generated the meridional decrease of DCo along the southward large-scale circulation in the deep western Atlantic. Furthermore, the apparent scavenged profile of DCo observed in the deep waters likely resulted from the persistence of relatively high concentrations in intermediate waters and low DCo concentrations in underlaying bottom waters. We suggest that the 2010 Icelandic volcanic eruption could have been a source of DCo that could have been transported into the core of the Northeast Atlantic Deep Waters. At intermediate depths, the high concentrations of DCo recorded in the ACW linearly correlated with the apparent utilization of oxygen (AOU), indicating that remineralization of DCo could be significant (representing up to 37% of the DCo present). Furthermore, the preferential remineralization of phosphate (P) compared to Co in these low-oxygenated waters suggests a decoupling between the deep cycles of P and Co. The vertical diffusion of DCo from the ACW appears to be a significant source of DCo into the surface waters of the equatorial domain. Summarizing, the dilution due to mixing processes rather than scavenging of DCo and the above-mentioned remineralization could be the two major pathways controlling the cycling of DCo into the intermediate and deep western Atlanti

Distributions of particulate Heme <i>b</i> in the Atlantic and Southern Oceans— Implications for electron transport in phytoplankton

Concentrations of heme b, the iron-containing component of b-type hemoproteins, ranged from?<?0.4 to 5.3 pM with an average of 1.18?±?0.8 pM (± 1s; n?=?86) in the Iceland Basin (IB), from?<?0.4 to 19.1 pM with an average of 2.24?±?1.67 pM (n?=?269) in the tropical northeast Atlantic (TNA) and from 0.6 to 21 pM with an average of 5.1?±?4.8 pM (n?=?34) in the Scotia Sea (SS). Heme b concentrations were enhanced in the photic zone and decreased with depth. Heme b concentrations correlated positively with chlorophyll a (chl a) in the TNA (r?=?0.41, p?<?0.01, n?=?269). Heme b did not correlate with chl a in the IB or SS. In the IB and SS, stations with high-chlorophyll and low-nutrient (Fe and/or Si) concentrations exhibited low heme b concentrations relative to particulate organic carbon (< 0.1?µmol?mol-1), and high chl a:heme b ratios (> 500). High chl a:heme b ratios resulted from relative decreases in heme b, suggesting proteins such as cytochrome b6f, the core complex of photosystem II, and eukaryotic nitrate reductase were depleted relative to proteins containing chlorophyll such as the eukaryotic light-harvesting antenna. Relative variations in heme b, particulate organic carbon, and chl a can thus be indicative of a physiological response of the phytoplankton community to the prevailing growth conditions, within the context of large-scale changes in phytoplankton community composition

Dissolved aluminium in the ocean conveyor of theWest Atlantic Ocean: Effects of the biological cycle, scavenging, sediment resuspension and hydrography

The concentrations of dissolved aluminium (dissolved Al) were studied along the West Atlantic GEOTRACESGA02 transect from 64°N to 50°S. Concentrations ranged from~0.5 nmol kg-1 in the high latitude surface watersto ~48 nmol kg-1 in surfacewaters around 25°N. Elevated surfacewater concentrations due to atmospheric dustloading have little influence on the deep water distribution. However, just belowthe thermocline, both Northernand Southern Hemisphere Subtropical Mode Waters are elevated in Al, most likely related to atmospheric dustdeposition in the respective source regions.In the deep ocean, high concentrations of up to 35 nmol kg-1 were observed in North Atlantic DeepWater as aresult of Al input via sediment resuspension. Comparatively lowdeepwater concentrationswere associatedwithwater masses of Antarctic origin. During water mass advection, Al loss by scavenging overrules input viaremineralisation and sediment resuspension at the basin wide scale. Nevertheless, sediment resuspension ismore important than previously realised for the deep ocean Al distribution and even more intensive samplingis needed in bottom waters to constrain the spatial heterogeneity in the global deep ocean.This thus far longest (17,500 km) full depth ocean section shows that the distribution of Al can be explained by itsinput sources and the combination of association with particles and release from those particles at depth, thelattermost likelywhen the particles remineralise. The association of Alwith particles can be due to incorporationof Al into biogenic silica or scavenging of Al onto biogenic particles. The interaction between Al and biogenicparticles can lead to the coupled cycling of Al and silicate that is observed in some ocean regions. However, inother regions this coupling is not observed due to (i) advective processes bringing in older water masses thatare depleted in Al, (ii) unfavourable scavenging conditions in the water column, (iii) low surface concentrationsof Al or (iv) additional Al sources, notably sediment resuspension

Neodymium isotopic composition and concentration in the western North Atlantic Ocean: Results from the GEOTRACES GA02 section

The neodymium (Nd) isotopic composition of seawater is commonly used as a proxy to study past changes in the thermohaline circulation. The modern database for such reconstructions is however poor and the understanding of the underlying processes is incomplete. Here we present new observational data for Nd isotopes and concentrations from twelve seawater depth profiles, which follow the flow path of North Atlantic Deep Water (NADW) from its formation region in the North Atlantic to the northern equatorial Atlantic. Samples were collected during two cruises constituting the northern part of the Dutch GEOTRACES transect GA02 in 2010. The results show that the different water masses in the subpolar North Atlantic Ocean, which ultimately constitute NADW, have the following Nd isotope characteristics: Upper Labrador Sea Water (ULSW), eNd = -14.2 ± 0.3; Labrador Sea Water (LSW), eNd = -13.7 ± 0.9; Northeast Atlantic Deep Water (NEADW), eNd = -12.5 ± 0.6; Northwest Atlantic Bottom Water (NWABW), eNd = -11.8 ± 1.4. In the subtropics, where these source water masses have mixed to form NADW, which is exported to the global ocean, upper-NADW is characterised by eNd values of -13.2 ± 1.0 (2sd) and lower-NADW exhibits values of eNd = -12.4 ± 0.4 (2sd). While both signatures overlap within error, the signature for lower-NADW is significantly more radiogenic than the traditionally used value for NADW (eNd = -13.5) due to the dominance of source waters from the Nordic Seas (NWABW and NEADW). Comparison between the concentration profiles and the corresponding Nd isotope profiles with other water mass properties such as salinity, silicate concentrations, neutral densities and chlorofluorocarbon (CFC) concentration provides novel insights into the geochemical cycle of Nd and reveals that different processes are necessary to account for the observed Nd characteristics in the subpolar and subtropical gyres and throughout the vertical water column. While our data set provides additional insights into the contribution of boundary exchange in areas of sediment resuspension, the results for open ocean seawater demonstrate, at an unprecedented level, the suitability of Nd isotopes to trace modern water masses in the strongly advecting western Atlantic Ocean

Importance of hydrothermal vents in scavenging removal of ²³⁰Th in the Nansen Basin

In this study we present dissolved and particulate ²³⁰Th and ²³²Th results, as well as particulate ²³⁴Th data, obtained as part of the GEOTRACES central Arctic Ocean sections GN04 (2015) and IPY11 (2007). Samples were analyzed following GEOTRACES methods and compared to previous results from 1991. We observe significant decreases in ²³⁰Th concentrations in the deep waters of the Nansen Basin. We ascribe this nonsteady state removal process to a variable release and scavenging of trace metals near an ultraslow spreading ridge. This finding demonstrates that hydrothermal scavenging in the deep‐sea may vary on annual time scales and highlights the importance of repeated GEOTRACES sections

20 years of the Atlantic Meridional Transect - AMT

The AMT (www.amt-uk.org) is a multidisciplinary programme which undertakes biological, chemical, and physical oceanographic research during an annual voyage between the UK and a destination in the South Atlantic such as the Falkland Islands, South Africa, or Chile. This transect of >12,000 km crosses a range of ecosystems from subpolar to tropical, from euphotic shelf seas and upwelling systems, to oligotrophic mid-ocean gyres. The year 2015 has seen two milestones in the history of the AMT: the achievement of 20 years of this unique ocean going programme and the departure of the 25th cruise on the 15th of September. Both of these events were celebrated in June this year with an open science conference hosted by the Plymouth Marine Laboratory (PML) and will be further documented in a special issue of Progress in Oceanography which is planned for publication in 2016. Since 1995, the 25 research cruises have involved 242 sea-going scientists from 66 institutes representing 22 countries. AMT was designed from the outset to be a collaborative programme. It was originally conceived by Jim Aiken, Patrick Holligan, Roger Harris, and Dave Robins with Chuck McClain and Chuck Trees at NASA to test and ground truth satellite algorithms of ocean color. The opportunities offered by this initiative meant that this series of repeated biannual cruises rapidly developed into a coordinated study of ocean biodiversity, biogeochemistry, and ocean/atmosphere interactions

A critical look at the calculation of the binding characteristics and concentration of iron complexing ligands in seawater with suggested improvements

Environmental context<br>The low concentration of iron in the oceans limits growth of phytoplankton. Dissolved organic molecules, called ligands, naturally present in seawater, bind iron thereby increasing its solubility and, consequently, its availability for biological uptake by phytoplankton. The characteristics of these ligands are determined indirectly with various mathematical solutions; we critically evaluate the underlying method and calculations used in these determinations.<br>The determination of the thermodynamic characteristics of organic Fe binding ligands, total ligand concentration ([L-t]) and conditional binding constant (K '), by means of titration of natural ligands with Fe in the presence of an added known competing ligand, is an indirect method. The analysis of the titration data including the determination of the sensitivity (S) and underlying model of ligand exchange is discussed and subjected to a critical evaluation of its underlying assumptions. Large datasets collected during the International Polar Year, were used to quantify the error propagation along the determination procedure. A new and easy to handle non-linear model written in R to calculate the ligand characteristics is used. The quality of the results strongly depends on the amount of titration points or Fe additions in a titration. At least four titration points per distinguished ligand group, together with a minimum of four titration points where the ligands are saturated, are necessary to obtain statistically reliable estimates of S, K ' and [L-t]. As a result estimating the individual concentration of two ligands, although perhaps present, might not always be justified

Determination of nitrate and phosphate in seawater at nanomolar concentrations

Over much of the world’s surface oceans, nitrate and phosphate concentrations are below the limit of detection (LOD) of conventional techniques of analysis. However, these nutrients play a controlling role in primary productivity and carbon sequestration in these waters. In recent years, techniques have been developed to address this challenge, and methods are now available for the shipboard analysis of nanomolar (nM) nitrate and phosphate concentrations with a high sample throughput.This article provides an overview of the methods for nM nitrate and phosphate analysis in seawater. We outline in detail a system comprising liquid waveguide capillary cells connected to a conventional segmented-flow autoanalyser and using miniaturised spectrophotometers. This approach is suitable for routine field measurements of nitrate and phosphate and achieves LODs of 0.8 nM phosphate and 1.5 nM nitrate