ALBERT

Description: In this study we present dissolved and particulate 230 Th and 232 Th results, as well as particulate 234 Th 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 230 Th 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. ©2018. The Authors.

Description: The distributions of the bio-essential trace element dissolved Co (DCo) and the apparent particulate Co (PCo) are presented along the GEOTRACES-A02 deep section from 64° N to 50° S in the West Atlantic Ocean. PCo was determined as the difference between total cobalt (TCo, unfiltered samples) and DCo. DCo concentrations ranged from 14.7 pM 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) that appeared to be the major reservoir of DCo in the West Atlantic. In the Antarctic Bottom Waters, the enrichment in DCo with ageing 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 West 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 suggested that the 2010 Icelandic volcanic eruption can be a source of DCo that could have been transported in the core of the North-East 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 can be significant (representing up to 29% of the DCo present). Furthermore the preferential remineralization of phosphate (P) compared to Co in these low-oxygenated waters suggested a decoupling between the deep cycles of P and Co. The vertical diffusion of DCo from the ACW appeared to be a significant source of DCo into the surface waters of the equatorial domain. Summarizing the dilution and mixing processes rather than scavenging of DCo, and the remineralization can be the two major pathways controlling the cycling of DCo in the intermediate and deep West Atlantic.

Description: The 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 (TCo, unfiltered samples) and DCo. DCo concentrations ranged from 14.7 pM 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 Atlantic.

Description: Oceanic fixed-nitrogen concentrations are controlled by the balance between nitrogen fixation and denitrification. A number of factors, including iron limitation, can restrict nitrogen fixation, introducing the potential for decoupling of nitrogen inputs and losses. Such decoupling could significantly affect the oceanic fixed-nitrogen inventory and consequently the biological component of ocean carbon storage and hence air–sea partitioning of carbon dioxide. However, the extent to which nutrients limit nitrogen fixation in the global ocean is uncertain. Here, we examined rates of nitrogen fixation and nutrient concentrations in the surface waters of the Atlantic Ocean along a north–south 10,000 km transect during October and November 2005. We show that rates of nitrogen fixation were markedly higher in the North Atlantic compared with the South Atlantic Ocean. Across the two basins, nitrogen fixation was positively correlated with dissolved iron and negatively correlated with dissolved phosphorus concentrations. We conclude that inter-basin differences in nitrogen fixation are controlled by iron supply rather than phosphorus availability. Analysis of the nutrient content of deep waters suggests that the fixed nitrogen enters North Atlantic Deep Water. Our study thus supports the suggestion that iron significantly influences nitrogen fixation5, and that subsequent interactions with ocean circulation patterns contribute to the decoupling of nitrogen fixation and loss.

Description: 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. © 2008 Elsevier Ltd. All rights reserved.

Description: Aeolian dust transport from the Saharan/Sahel desert regions is considered the dominant external input of iron (Fe) to the surface waters of the eastern (sub-) tropical North Atlantic Ocean. To test this hypothesis, we investigated the sources of dissolved Fe (DFe) and quantified DFe fluxes to the surface ocean in this region. In winter 2008, surface water DFe concentrations varied between 〈0.1 nM and 0.37 nM, with an average of 0.13 ̃ 0.07 nM DFe (n = 194). A strong correlation between mixed layer averaged concentrations of dissolved aluminum (DAl), a proxy for dust input, and DFe indicated dust as a source of DFe to the surface ocean. The importance of Aeolian nutrient input was further confirmed by an increase of 0.1 nM DFe and 0.05 μM phosphate during a repeat transect before and after a dust event. An exponential decrease of DFe with increasing distance from the African continent, suggested that continental shelf waters were a source of DFe to the northern part of our study area. Relatively high Fe:C ratios of up to 3 ° 10°5 (C derived from apparent oxygen utilization (AOU)) indicated an external source of Fe to these African continental shelf waters. Below the wind mixed layer along 12°N, enhanced DFe concentrations (〉1.5 nM) correlated positively with apparent oxygen utilization (AOU) and showed the importance of organic matter remineralization as an DFe source. As a consequence, vertical diffusive mixing formed an important Fe flux to the surface ocean in this region, even surpassing that of a major dust event. © 2012. American Geophysical Union.

Description: Concentrations of dissolved iron (DFe) and Fe-binding ligands were determined in the tropical Northeast Atlantic Ocean (12-30°N, 21-29°W) as part of the UK-SOLAS (Surface Ocean Lower Atmosphere Study) cruise Poseidon 332 (P332) in January-February 2006. The surface water DFe concentrations varied between 0.1 and 0.4 nM with an average of 0.22 ± 0.05 nM (n = 159). The surface water concentrations of total Fe-binding ligands varied between 0.82 and 1.46 nM with an average of 1.11 ± 0.14 nM (n = 33). The concentration of uncomplexed Fe-binding ligands varied between 0.64 and 1.35 nM with an average of 0.90 ± 0.14 nM (n = 33). Thus, on average 81 of the total Fe-binding ligand concentration was uncomplexed. The average logarithmic conditional stability constant of the pool of Fe-binding ligands was 22.85 ± 0.38 with respect to Fe 3+ (n = 33). A transect (12°N, 26°W to 16°N, 25.3°W) was sailed during a small Saharan dust event and repeated a week later. Following the dust event, the concentration of DFe increased from 0.20 ± 0.026 nM (n = 125) to 0.25 ± 0.028 (n = 17) and the concentration of free Fe-binding ligands decreased from 1.15 ± 0.15 (n = 4) to 0.89 ± 0.10 (n = 4) nM. Furthermore, the logarithmic stability constants of the Fe-binding ligands south of the Cape Verde islands were distinctively lower than north of the islands. The absence of a change in the logarithmic stability constant after the dust event south of the Cape Verde islands suggests that there was no significant atmospheric input of new Fe-binding ligands during this dust event.

Description: This paper reports on investigations into interferences with the measurements of nanomolar nitrate. +. nitrite and soluble reactive phosphate (SRP) in oceanic surface seawater using a segmented continuous flow autoanalyser (SCFA) interfaced with a liquid-waveguide capillary flow-cell (LWCC). The interferences of silicate and arsenate with the analysis of SRP, the effect of sample filtration on the measurement of nanomolar nitrate. +. nitrite and SRP concentrations, and the stability of samples during storage are described.The investigation into the effect of arsenate (concentrations up to 100nM) on phosphate analysis (concentrations up to 50nM) indicated that the arsenate interference scaled linearly with phosphate concentrations, resulting in an overestimation of SRP concentrations of 4.6±1.4 for an assumed arsenate concentration of 20nM. The effect of added Si(OH)4 was to increase SRP signals by up to 36±19nM (at 100μM Si(OH)4). However, at silicate concentrations below 1.5μM, which are typically observed in oligotrophic surface ocean waters, the effect of silicate on the phosphate analysis was much smaller (≤0.78±0.15nM change in SRP). Since arsenate and silicate interferences vary between analytical approaches used for nanomolar SRP analysis, it is important that the interferences are systematically assessed in any newly developed analytical system.Filtration of surface seawater samples resulted in a decrease in concentration of 1.7-2.7. nM (±0.5. nM) SRP, and a small decrease in nitrate concentrations which was within the precision of the method (±0.6. nM). A stability study indicated that storage of very low concentration nutrient samples in the dark at 4°C for less than 24. h resulted in no statistically significant changes in nutrient concentrations. Freezing unfiltered surface seawater samples from an oligotrophic ocean region resulted in a small but significant increase in the SRP concentration from 12.0 ± 1.3 nM (n=3) to 14.7 ± 0.6. nM (n=3) (Student's t-test; p=0.021). The corresponding change in nitrate concentration was not significant (Student's t-test; p>0.05). © 2010 Elsevier B.V.