_version_ 1867171356710273024
author Croot, Peter L
Laan, Patrick
Nishioka, Jun
Strass, Volker H
Cisewski, Boris
Boyé, Marie
Timmermans, Klaas R
Bellerby, Richard G J
Goldson, Laura
Nightingale, Philip D
de Baar, Hein J W
author_facet Croot, Peter L
Laan, Patrick
Nishioka, Jun
Strass, Volker H
Cisewski, Boris
Boyé, Marie
Timmermans, Klaas R
Bellerby, Richard G J
Goldson, Laura
Nightingale, Philip D
de Baar, Hein J W
collection Datos científicos de ciencias marinas y ambientales
contents Measurements of Fe(II) and H2O2 were carried out in the Atlantic sector of the Southern Ocean during EisenEx, an iron enrichment experiment. Iron was added on three separate occasions, approximately every 8 days, as a ferrous sulfate (FeSO4) solution. Vertical profiles of Fe(II) showed maxima consistent with the plume of the iron infusion. While H2O2 profiles revealed a corresponding minima showing the effect of oxidation of Fe(II) by H2O2, observations showed detectable Fe(II) concentrations existed for up to 8 days after an iron infusion. H2O2 concentrations increased at the depth of the chlorophyll maximum when iron concentrations returned to pre-infusion concentrations (<80 pM) possibly due to biological production related to iron reductase activity. In this work, Fe(II) and dissolved iron were used as tracers themselves for subsequent iron infusions when no further SF6 was added. EisenEx was subject to periods of weak and strong mixing. Slow mixing after the second infusion allowed significant concentrations of Fe(II) and Fe to exist for several days. During this time, dissolved and total iron in the infusion plume behaved almost conservatively as it was trapped between a relict mixed layer and a new rain-induced mixed layer. Using dissolved iron, a value for the vertical diffusion coefficient Kz=6.7±0.7 cm**2/s was obtained for this 2-day period. During a subsequent surface survey of the iron-enriched patch, elevated levels of Fe(II) were found in surface waters presumably from Fe(II) dissolved in the rainwater that was falling at this time. Model results suggest that the reaction between uncomplexed Fe(III) and O2? was a significant source of Fe(II) during EisenEx and helped to maintain high levels of Fe(II) in the water column. This phenomenon may occur in iron enrichment experiments when two conditions are met: (i) When Fe is added to a system already saturated with regard to organic complexation and (ii) when mixing processes are slow, thereby reducing the dispersion of iron into under-saturated waters.
format Dataset Open Access
id pangaea_https___doi_org_10_1594_PANGAEA_701303
institution PANGAEA
language en
publishDate 2008
publisher PANGAEA
record_format pangaea
spellingShingle Dissolved iron measured along surface transects of the CARUSO-EISENEX experiment
Croot, Peter L
Laan, Patrick
Nishioka, Jun
Strass, Volker H
Cisewski, Boris
Boyé, Marie
Timmermans, Klaas R
Bellerby, Richard G J
Goldson, Laura
Nightingale, Philip D
de Baar, Hein J W
ANT-XVIII/2; CT; EisenEx; European Iron Enrichment Experiment in the Southern Ocean; Polarstern; Priority Programme 1158 Antarctic Research with Comparable Investigations in Arctic Sea Ice Areas; PS58_transect01; PS58_transect02; PS58_transect03; PS58_transect04; PS58_transect05; PS58_transect06; PS58_transect07; PS58_transect08; PS58_transect09; PS58_transect10; PS58_transect11; PS58 EISENEX; SPP1158; Underway cruise track measurements
Measurements of Fe(II) and H2O2 were carried out in the Atlantic sector of the Southern Ocean during EisenEx, an iron enrichment experiment. Iron was added on three separate occasions, approximately every 8 days, as a ferrous sulfate (FeSO4) solution. Vertical profiles of Fe(II) showed maxima consistent with the plume of the iron infusion. While H2O2 profiles revealed a corresponding minima showing the effect of oxidation of Fe(II) by H2O2, observations showed detectable Fe(II) concentrations existed for up to 8 days after an iron infusion. H2O2 concentrations increased at the depth of the chlorophyll maximum when iron concentrations returned to pre-infusion concentrations (<80 pM) possibly due to biological production related to iron reductase activity. In this work, Fe(II) and dissolved iron were used as tracers themselves for subsequent iron infusions when no further SF6 was added. EisenEx was subject to periods of weak and strong mixing. Slow mixing after the second infusion allowed significant concentrations of Fe(II) and Fe to exist for several days. During this time, dissolved and total iron in the infusion plume behaved almost conservatively as it was trapped between a relict mixed layer and a new rain-induced mixed layer. Using dissolved iron, a value for the vertical diffusion coefficient Kz=6.7±0.7 cm**2/s was obtained for this 2-day period. During a subsequent surface survey of the iron-enriched patch, elevated levels of Fe(II) were found in surface waters presumably from Fe(II) dissolved in the rainwater that was falling at this time. Model results suggest that the reaction between uncomplexed Fe(III) and O2? was a significant source of Fe(II) during EisenEx and helped to maintain high levels of Fe(II) in the water column. This phenomenon may occur in iron enrichment experiments when two conditions are met: (i) When Fe is added to a system already saturated with regard to organic complexation and (ii) when mixing processes are slow, thereby reducing the dispersion of iron into under-saturated waters.
title Dissolved iron measured along surface transects of the CARUSO-EISENEX experiment
topic ANT-XVIII/2; CT; EisenEx; European Iron Enrichment Experiment in the Southern Ocean; Polarstern; Priority Programme 1158 Antarctic Research with Comparable Investigations in Arctic Sea Ice Areas; PS58_transect01; PS58_transect02; PS58_transect03; PS58_transect04; PS58_transect05; PS58_transect06; PS58_transect07; PS58_transect08; PS58_transect09; PS58_transect10; PS58_transect11; PS58 EISENEX; SPP1158; Underway cruise track measurements
url https://doi.org/10.1594/PANGAEA.701303