ALBERT

Description: We report detailed sections of radium-226 (226Ra, T1/2 = 1602 y) activities and barium (Ba) concentrations determined in the North Atlantic (Portugal-Greenland-Canada) in the framework of the international GEOTRACES program (GA01 section – GEOVIDE project, May–July 2014). Dissolved 226Ra and Ba are strongly correlated along the GA01 section, a pattern that reflects their similar chemical behavior. Since 226Ra and Ba have been widely used as tracers of water masses and ocean mixing, we investigated more thoroughly their behavior in this crucial region for thermohaline circulation taking advantage of the contrasting biogeochemical patterns existing along the GA01 section. We used an Optimum Multiparameter (OMP) analysis to distinguish the relative importance of physical transport (water mass mixing) from non-conservative processes (sedimentary, river, or hydrothermal inputs; uptake by particles, and dissolved-particulate dynamics) on the 226Ra and Ba distributions in the North Atlantic. Results show that 72 % of the 226Ra and 68 % of the Ba can be explained by conservative mixing along the section and therefore, they can be considered as conservative tracers of water mass transport in the ocean interior. However, regions where 226Ra and Ba displayed non-conservative behavior were also identified, mostly at the ocean boundaries (seafloor, continental margins, and surface waters). Elevated 226Ra and Ba concentrations found in deep waters of the West European Basin reflect that lower North East Atlantic Deep Water (NEADWl) accumulates excess 226Ra and Ba from sediment diffusion during transport. In the upper 1500 m, deficiencies in 226Ra and Ba are likely explained by their incorporation in planktonic siliceous shells, or in barite (BaSO4) (Bishop, 1988). Finally, since Ba and 226Ra display different source terms (mostly deep-sea sediments for 226Ra and rivers for Ba), strong decoupling between 226Ra and Ba were observed at the land-ocean boundaries. This is especially true in the shallow stations near the coasts of Greenland and Newfoundland where high 226Ra / Ba ratios at depth reflect the diffusion of 226Ra from sediment and low 226Ra / Ba ratios in the upper water column reflect the input of Ba associated with meteoric waters.

Description: We report detailed sections of radium-226 (226Ra, T1∕2 =  1602 years) activities and barium (Ba) concentrations determined in the North Atlantic (Portugal–Greenland–Canada) in the framework of the international GEOTRACES program (GA01 section – GEOVIDE project, May–July 2014). Dissolved 226Ra and Ba are strongly correlated along the section, a pattern that may reflect their similar chemical behavior. Because 226Ra and Ba have been widely used as tracers of water masses and ocean mixing, we investigated their behavior more thoroughly in this crucial region for thermohaline circulation, taking advantage of the contrasting biogeochemical patterns existing along the GA01 section. We used an optimum multiparameter (OMP) analysis to distinguish the relative importance of physical transport (water mass mixing) from nonconservative processes (sedimentary, river or hydrothermal inputs, uptake by particles and dissolved–particulate dynamics) on the 226Ra and Ba distributions in the North Atlantic. Results show that the measured 226Ra and Ba concentrations can be explained by conservative mixing for 58 and 65 % of the samples, respectively, notably at intermediate depth, away from the ocean interfaces. 226Ra and Ba can thus be considered conservative tracers of water mass transport in the ocean interior on the space scales considered here, namely, on the order of a few thousand kilometers. However, regions in which 226Ra and Ba displayed nonconservative behavior and in some cases decoupled behaviors were also identified, mostly at the ocean boundaries (seafloor, continental margins and surface waters). Elevated 226Ra and Ba concentrations found in deepwater in the West European Basin suggest that lower Northeast Atlantic Deep Water (NEADWl) accumulates 226Ra and Ba from sediment diffusion and/or particle dissolution during transport. In the upper 1500 m of the West European Basin, deficiencies in 226Ra and Ba are likely explained by their incorporation in planktonic calcareous and siliceous shells, or in barite (BaSO4) by substitution or adsorption mechanisms. Finally, because Ba and 226Ra display different source terms (mostly deep-sea sediments for 226Ra and rivers for Ba), strong decoupling between 226Ra and Ba were observed at the land–ocean boundaries. This is especially true in the shallow stations near the coasts of Greenland and Newfoundland where high 226Ra ∕ Ba ratios at depth reflect the diffusion of 226Ra from sediment and low 226Ra ∕ Ba ratios in the upper water column reflect the input of Ba associated with meteoric waters.

Description: In the ocean, remineralization rate associated with sinking particles is a crucial variable. Since the 1990s, particulate biogenic barium (Baxs) has been used as an indicator of carbon remineralization by applying a transfer function relating Baxs to O2 consumption (Dehairs's transfer function, Southern Ocean-based). Here, we tested its validity in the Mediterranean Sea (ANTARES/EMSO-LO) for the first time by investigating connections between Baxs, prokaryotic heterotrophic production (PHP) and oxygen consumption (JO2-Opt; optodes measurement). We show that (1) higher Baxs (409 pM; 100–500 m) occurs in situations where integrated PHP (PHP100/500=0.90) is located deeper, (2) higher Baxs occurs with increasing JO2-Opt, and (3) there is similar magnitude between JO2-Opt (3.14 mmol m−2 d−1; 175–450 m) and JO2-Ba (4.59 mmol m−2 d−1; transfer function). Overall, Baxs, PHP and JO2 relationships follow trends observed earlier in the Southern Ocean. We conclude that such a transfer function could apply in the Mediterranean Sea.

Description: © The Author(s), 2018. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Biogeosciences 15 (2018): 3027-3048, doi:10.5194/bg-15-3027-2018.

Description: We report detailed sections of radium-226 (226Ra, T1∕2 =  1602 years) activities and barium (Ba) concentrations determined in the North Atlantic (Portugal–Greenland–Canada) in the framework of the international GEOTRACES program (GA01 section – GEOVIDE project, May–July 2014). Dissolved 226Ra and Ba are strongly correlated along the section, a pattern that may reflect their similar chemical behavior. Because 226Ra and Ba have been widely used as tracers of water masses and ocean mixing, we investigated their behavior more thoroughly in this crucial region for thermohaline circulation, taking advantage of the contrasting biogeochemical patterns existing along the GA01 section. We used an optimum multiparameter (OMP) analysis to distinguish the relative importance of physical transport (water mass mixing) from nonconservative processes (sedimentary, river or hydrothermal inputs, uptake by particles and dissolved–particulate dynamics) on the 226Ra and Ba distributions in the North Atlantic. Results show that the measured 226Ra and Ba concentrations can be explained by conservative mixing for 58 and 65 % of the samples, respectively, notably at intermediate depth, away from the ocean interfaces. 226Ra and Ba can thus be considered conservative tracers of water mass transport in the ocean interior on the space scales considered here, namely, on the order of a few thousand kilometers. However, regions in which 226Ra and Ba displayed nonconservative behavior and in some cases decoupled behaviors were also identified, mostly at the ocean boundaries (seafloor, continental margins and surface waters). Elevated 226Ra and Ba concentrations found in deepwater in the West European Basin suggest that lower Northeast Atlantic Deep Water (NEADWl) accumulates 226Ra and Ba from sediment diffusion and/or particle dissolution during transport. In the upper 1500 m of the West European Basin, deficiencies in 226Ra and Ba are likely explained by their incorporation in planktonic calcareous and siliceous shells, or in barite (BaSO4) by substitution or adsorption mechanisms. Finally, because Ba and 226Ra display different source terms (mostly deep-sea sediments for 226Ra and rivers for Ba), strong decoupling between 226Ra and Ba were observed at the land–ocean boundaries. This is especially true in the shallow stations near the coasts of Greenland and Newfoundland where high 226Ra ∕ Ba ratios at depth reflect the diffusion of 226Ra from sediment and low 226Ra ∕ Ba ratios in the upper water column reflect the input of Ba associated with meteoric waters.

Description: The present research and Emilie Le Roy’s fellowship are co-funded by the European Union and the Région Occitanie-Pyrénées-Méditerranée (European Regional Development Fund). This work was also co-funded by the French national program LEFE/INSU “REPAP” (PI Stéphanie H. M Jacquet) and the US National Science Foundation (PI Matthew A. Charette, OCE-1458305; OCE-1232669). For this work Maribel I. García-Ibáñez and Fiz F. Pérez were supported by the Spanish Ministry of Economy and Competitiveness through the BOCATS (CTM2013-41048-P) project co-funded by the Fondo Europeo de Desarrollo Regional 2014–2020 (FEDER).

Description: Author Posting. © Elsevier B.V., 2008. This is the author's version of the work. It is posted here by permission of Elsevier B.V. for personal use, not for redistribution. The definitive version was published in Deep Sea Research Part II: Topical Studies in Oceanography 55 (2008): 1673-1683, doi:10.1016/j.dsr2.2008.04.020.

Description: This study focuses on the fate of exported organic carbon in the twilight zone at two contrasting environments in the North Pacific: the oligotrophic ALOHA site (22°45' N 158°W; Hawaii; studied during June–July 2004) and the mesotrophic Subarctic Pacific K2 site (47°N, 161°W; studied during July-August 2005). Earlier work has shown that non-lithogenic, excess particulate Ba (Baxs) in the mesopelagic water column is a potential proxy of organic carbon remineralization. In general Baxs contents were significantly larger at K2 than at ALOHA. At ALOHA the Baxs profiles from repeated sampling (5 casts) showed remarkable consistency over a period of three weeks, suggesting that the system was close to being at steady state. In contrast, more variability was observed at K2 (6 casts sampled) reflecting the more dynamic physical and biological conditions prevailing in this environment. While for both sites Baxs concentrations increased with depth, at K2 a clear maximum was present between the base of the mixed layer at around 50m and 500m, reflecting production and release of Baxs. Larger mesopelagic Baxs contents and larger bacterial production in the twilight zone at the K2 site indicate that more material was exported from the upper mixed layer for bacterial degradation deeper, compared to the ALOHA site. Furthermore, application of a published transfer function (Dehairs et al., 1997) relating oxygen consumption to the observed Baxs data indicated that the latter were in good agreement with bacterial respiration, calculated from bacterial production. These results corroborate earlier findings highlighting the potential of Baxs as a proxy for organic carbon remineralization. The range of POC remineralization rates calculated from twilight zone excess particulate Ba contents did also compare well with the depth dependent POC flux decrease as recorded by neutrally buoyant sediment traps, except in 1 case (out of 4). This discrepancy could indicate that differences in sinking velocities cause an 3 uncoupling of the processes occurring in the fine suspended particle pool from those affecting the larger particle pool which sustains the vertical flux, thus rendering comparison between both approaches risky.

Description: This research was supported by Federal Science Policy Office, Brussels through contracts EV/03/7A, SD/CA/03A, the Research Foundation Flanders through grant G.0021.04 and Vrije Universiteit Brussel via grant GOA 22, as well as the US National Science Foundation programs in Chemical and Biological Oceanography.