Abstract

The iron fertilization experiment LOHAFEX was conducted in a cold-core eddy in the Southern Atlantic Ocean during austral summer. Within a few days after fertilization, a phytoplankton bloom developed dominated by nano- and picoplankton groups. Unlike previously reported for other iron fertilization experiments, a diatom bloom was prevented by iron and silicate co-limitation. We used 18S rRNA gene tag pyrosequencing to investigate the diversity of these morphologically similar cell types within the nano- and picoplankton and microscopically enumerated dominant clades after catalyzed reported deposition fluorescence in situ hybridization (CARD-FISH) with specific oligonucleotide probes. In addition to Phaeocystis, members of Syndiniales group II, clade 10–11, and the Micromonas clades ABC and E made up a major fraction of the tag sequences of the nano- and picoplankton community within the fertilized patch. However, the same clades were also dominant before the bloom and outside the fertilized patch. Furthermore, only little changes in diversity could be observed over the course of the experiment. These results were corroborated by CARD-FISH analysis which confirmed the presence of a stable nano- and picoplankton community dominated by Phaeocystis and Micromonas during the entire course of the experiment. Interestingly, although Syndiniales dominated the tag sequences, they could hardly be detected by CARD-FISH, possibly due to the intracellular parasitic life style of this clade. The remarkable stability of the nano- and picoplankton community points to a tight coupling of the different trophic levels within the microbial food web during LOHAFEX.

Highlights

  • Phytoplankton blooms occur seasonally in large parts of the oceans

  • Among the Stramenopiles, the most dominant operational taxonomic units (OTUs) belonged to the Marine Stramenopiles (MAST)-1 clade (,2%), and the MAST-3 clade (0.4–2.1%)

  • The bulk of OTUs within the Stramenopiles accounted for 4–10% of the sequences

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Summary

Introduction

Phytoplankton blooms occur seasonally in large parts of the oceans. Typically, a spring or upwelling bloom dominated by large diatoms is followed closely by a community dominated by small nanoplankton. Wide ocean areas exhibit low phytoplankton standing stocks despite perennially high nutrient concentrations. Such high nutrient - low chlorophyll areas (HNLCs) are present in the subarctic and equatorial Pacific Ocean and in most of the Southern Ocean. In the following years a dozen Lagrangian experiments in iron-limited HNLC waters have shown that phytoplankton blooms can be induced by artificial iron fertilization [2]. To quantify the extent of carbon export of phytoplankton biomass and the impact of the microbial loop in surface waters the Indo-German iron fertilization experiment LOHAFEX (‘loha’ is Hindi for ‘iron’; FEX for Fertilization EXperiment) was conducted in late austral summer of 2009 in a cold core eddy north of the Antarctic Polar Front in the Atlantic sector of the subantarctic Southern Ocean. During LOHAFEX mainly Phaeocystis-like small flagellated and non-flagellated taxa dominated the bloom upon fertilization and only little export could be measured which was possibly the consequence of the co-limitation of dissolved iron and silica in the fertilized patch [12,13,14]

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