Dataset: BATS/Hydrostation S: Iodine speciation and isotope ratio values
Deployment: AE1825

Seawater was collected from the Bermuda Atlantic Time Series (BATS) and Hydrostation S (Hydro) sites in the Sargasso Sea in September 2018.  Depth profile investigations at BATS were taken at 32.343⁰N 64.594⁰W at 21 separate depths between 1m and 4500m.  Hydrostation S samples were taken at 32.165⁰N 64.501⁰W at 10 depths between 1m and 500m.  Incubation water was taken from two depths (1m and 240m) and collected into four carboys (two euphotic (1m) and two subphotic (240m)).  One carboy from each depth was filtered using a 0.2µm filter to remove bacteria and other biology and particles while another was left unfiltered.  129I (t1/2  ~15.7 My) (Eckert and Ziegler Isotope Products ©) (Hardisty et al., 2020, Hardisty et al., 2021), was added directly to each of the carboys at a targeted concentration of ~70nM 129I- for investigating iodine redox reactions in natural seawater over time.  129I- was added before aliquoting the carboy water for individual incubations to ensure homogenous 129I- concentrations at t0 for all incubations.  200ml from each carboy were fractionated into separated incubation containers.  Samples for t0 were immediately subsampled from spiked incubation containers, with this and subsequent (t1, t2, tf) subsamples being ~50ml.  All subsamples were immediately filtered at 0.2µm to end interaction with biology after sampling.  Subsamples were refrigerated and stored at 4°C until they returned to Michigan State University and were frozen for storage.

Five incubation factors were used to create 20 incubation trials using a ship-deck light-filtering incubator to mimic at-depth light filtration, cooled with a continuous flow of ambient surface seawater and stored in translucent and amber Nalgene bottles for dark incubations: each done in triplicate.  Factors included: 1) filtering of samples through a 0.2µm syringe filter, meant as a control to screen filtered seawater of bacteria and macro-organisms and particles, kept in either the light or the dark depending on incubation, (Campos et al., 1996, Farrenkoph et al., 1997, Hardisty et al., 2020); 2) addition of O2− dismutase (SOD) to incubations both filtered and unfiltered, but all left in the dark, intended as a control to remove ambient O2− in seawater (Sutherland et al., 2020, Li et al., 2012, Diaz et al., 2013); 3) addition of superoxide thermal source (SOTS) and hydrogen peroxide (H2O2) to filtered samples kept in the dark in separate experiments, both suspected of being able to aid in oxidation of I- to IO3- in seawater, 4) unfiltered water in the dark to determine the role, if any, of photochemical reactions that may cause the reduction of IO3- to I- in the presence of organic matter (Chance et al., 2014, Spokes and Liss 1996); five additions of MnCl2 to iterations of the above in order to consider the potential of preferential Mn2+ oxidation relative to I-.  Note that controls 2 and 5 were only relevant if I- oxidation was detected in the other controls.

Seawater for samples was taken from both photic (1m) and subphotic (240m) depths and collected in carboys.  Superoxide thermal source was kept frozen (-80⁰C) until it was added by pipette to two of the incubations (11 and 19) as a combination of 1ml dimethyl sulfoxide (DMSO) + 1mg SOTS (3027.55µM SOTS) (Cayman Chemicals, CAS number 223507-96-8) at a volume targeting 10 nM O2− (Heller and Croot, 2010).  This was made fresh daily immediately before adding to samples and added daily to account for natural decay.  The O2− concentration of the SOTS stock was not analyzed but O2− concentration was analyzed in one experiment a few hours post-SOTS addition – to allow to reach steady state concentrations – to confirm O2− accumulation near target levels. Hydrogen peroxide (30%) was added at a volume targeting 50nM H2O2 in each solution.  SOD was added by pipette daily – thus accounting for decay and titration via potentially newly formed O2− within the incubations – from a stock volume of 4kU/ml to incubations to produce samples with SOD volume of 0.32kU/ml.  Given potential long oxidation timescales of I-, all incubations were performed over a 140-hour time period, with subsamples collected for iodine species measurement at t0, ~t40, ~t88, and ~t140 hours.

The concentrations of IO3- and I- from the incubations were determined at MSU after sample collection via the methods outlined by Jickells (1988) for spectrophotometry (IO3-) and by Hardisty et al., (2020) for ion exchange chromatography (I-, DOI) and ICP-MS.

Iodine isotope ratios were determined via the methods outlined in Hardisty et al., (2020) and Hardisty et al., (2021) using chromatographic separation and subsequent analysis via multi-collector ICP-MS (MC-ICP-MS).

See the related dataset "BATS/Hydrostation S: iodine speciation and superoxide concentration" (https://www.bco-dmo.org/dataset/914955) for details of the steady-state concentration of O2− methodology.