Abstract

The microbial degradation of marine particles is an important process in the remineralization of nutrients including iron. As part of the GEOTRACES process study (FeCycle II), we conducted incubation experiments with marine particles obtained from 30 and 100 m depth at two stations during austral spring in the subtropical waters east of the North Island of New Zealand. The particles were collected using in-situ pumps, and comprised mainly of suspended and slow sinking populations along with associated attached heterotrophic bacteria. In treatments with live bacteria, increasing concentrations of Fe binding ligands were observed with an average stability constant of logKFeL,Fe3+ = 21.11±0.37 for station 1 and 20.89±0.25 for station 2. The ligand release rates varied between 2.54 and 11.8 pmol L-1 d-1 (calculated for ambient seawater particle concentration) and were similar to those found in two Southern Ocean subsurface studies from ~110 m depths in subpolar and polar waters. Dissolved iron (DFe) was released at a rate between 0.33 and 2.09 pmol Fe L-1 d-1 with a column integrated (30 -100 m) flux of 107 and 58 nmol Fe m-2 day-1 at station 1 and 2, respectively. Given a mixed layer DFe inventory of ~48 µmol m-2 and ~4 µmol m-2 at the time of sampling for station 1 and 2, this will therefore result in a DFe residence time of 1.2 and 0.18 years, assuming particle remineralization was the only source of iron in the mixed layer. The DFe release rates calculated were comparable to those found in the previously mentioned study of Southern Ocean water masses. Fe-binding ligand producing bacteria (CAS positive) abundance was found to increase throughout the duration of the experiment of 7 to 8 days. For the first time ferrioxamine type siderophores, including the well-known ferrioxamine B and G, have been quantified using chemical assays and LC-ESI-MS. Our subtropical study corroborates prior reports from the Southern Ocean of particle remineralization being an important source of DFe and ligands, and adds unprecedented detail by revealing that siderophores are probably an important component of the ligands released into subsurface waters during particle remineralisation.

Highlights

  • Iron is an essential metal required for many microbial enzymatic activities (Geider and La Roche, 1994)

  • The natural Fe-siderophore complexes were identified using the natural Fe-isotopic ratio, which is a ratio of 56Fe/54Fe of 100/6.35 (De Hoffman and Stroobant, 1991). he criteria we looked for in details were: (1) ions that are bound to Fe should exhibit the Fe-isotopic pattern; (2) the 54Fe isotope is confirmed if natural abundance is within the range of 1–7% and the mass accuracy is within

  • It can be concluded that marine particles incubated in the dark were remineralized by attached bacteria and as a result Fe-binding ligands were produced at pM rates per day

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Summary

Introduction

Iron is an essential metal required for many microbial enzymatic activities (Geider and La Roche, 1994) It plays a central role in controlling primary production over much of the world’s ocean. Previous studies revealed that over 99.9% of dissolved iron in the ocean is bound by iron-complexing ligands (Gledhill and van den Berg, 1994; Van den Berg, 1995; Tian et al, 2006; Sander et al, 2015). These ironbinding ligands are separated into operational classes based on trends in conditional stability constants—L1 being the strongest Fe-binding ligand and L2,L3 etc. Other potential sources for iron binding ligand classes (L1 and weaker ligands) include virus lysis (Poorvin et al, 2011), exopolysaccharides (Hassler et al, 2011), and humic substances (Laglera and van den Berg, 2009; Abualhaija and van den Berg, 2014; Mahmood et al, 2015)

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