Mixotrophic haptophytes are key bacterial grazers in oligotrophic coastal waters

13 pages, 6 figures, 1 tableGrazing rate estimates indicate that approximately half of the bacterivory in oligotrophic oceans is due to mixotrophic flagellates (MFs). However, most estimations have considered algae as a single group. Here we aimed at opening the black-box of the phytoflagellates (PFs) <20 μm. Haptophytes, chlorophytes, cryptophytes and pigmented dinoflagellates were identified using fluorescent in situ hybridization or by standard 4′,6-diamidino-2- phenylindole staining. Their fluctuations in abundance, cell size, biomass and bacterivory rates were measured through an annual cycle in an oligotrophic coastal system. On average, we were able to assign to these groups: 37% of the total pico-PFs and 65% of the nano-PFs composition. Chlorophytes were mostly picoplanktonic and they never ingested fluorescently labeled bacteria. About 50% of the PF <20 μm biomass was represented by mixotrophic algae. Pigmented dinoflagellates were the least abundant group with little impact on bacterioplankton. Cryptophytes were quantitatively important during the coldest periods and explained about 4% of total bacterivory. Haptophytes were the most important mixotrophic group: (i) they were mostly represented by cells 3-5 μm in size present year-round; (ii) cell-specific grazing rates were comparable to those of other bacterivorous non-photosynthetic organisms, regardless of the in situ nutrient availability conditions; (iii) these organisms could acquire a significant portion of their carbon by ingesting bacteria; and (iv) haptophytes explained on average 40% of the bacterivory exerted by MFs and were responsible for 9-27% of total bacterivory at this site. Our results, when considered alongside the widespread distribution of haptophytes in the ocean, indicate that they have a key role as bacterivores in marine ecosystems. © 2014 International Society for Microbial Ecology All rights reservedThis study was supported by EU project BASICS (EVK3-CT-2002-00078) and a post-doctoral fellowship of the former MECD (SB2001-0166). It was also partially funded by MEC projects ESTRAMAR (CTM2004-12631/MAR), GENmMAR (CTM2004-02586/MAR) and FLAME (CGL2010-16304, MICINN), and by the Spanish-Argentina project PROBA (2007AR0018, CSIC). FN was supported by the Marie-Curie fellowship ESUMAST (MEIF-CT-2005-025000)Peer Reviewe