FP6Individual fellowship2006–2008

PAPHOS · Prokaryotic activity and phylogeny of oceanic systems

FP6 — Marie Curie Actions (Human Resources and Mobility)

Duration
2006-05-01 → 2008-04-30
EU contribution
€148,710
Participants
1
Scheme
EIF

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Results in brief

Final Activity Report Summary - PAPHOS (Prokaryotic activity and phylogeny of oceanic systems)

Prokaryotic plankton is the major drivers of biogeochemical cycles in the ocean. While the abundance and diversity of prokaryotic communities is well-known in surface waters, our knowledge about the bacteria and archaeal communities in the mesopelagic (200-1000 m depth) and bathypelagic (1000 - 5000 m depth) realms of the ocean, comprising about 70% of the ocean's volume, is rather rudimentary. Using fluorescence in situ hybridisation, it has been shown recently that planktonic Archaea, consisting of two major groups, the Crenarcheaota and Euryarchaeota, might account for about one-third of all prokaryotic cells in the global ocean. However, we still do not know the diversity and the functional importance of this archaeal community in deep waters and whether marine Archaea are important players in the biogeochemical cycles of the open ocean system. This project was mainly focused on the characterisation of the functional role and the diversity of microbial communities in meso- and bathypelagic waters of the North Atlantic. The first aim of this study was to examine the variability of bacterial and archaeal assemblages in different water masses of the eastern North Atlantic and to assess the prokaryotic diversity in its meso- and bathypelagic waters. T-RFLP (terminal restriction fragment length polymorphism) and cloning techniques, applied to the 16S rRNA gene, were used to decipher the community composition of bacterial and archaeal assemblages. Within distinct water masses, the composition of bacterial and archaeal communities was largely maintained even over large distances while vertical differences were pronounced. Based on our analyses, we conclude that for deep-water prokaryotic biogeography, the water masses exert more influence on the prokaryotic community composition than simply depth and that there is a pronounced stratification of the prokaryotic communities with distinct subsurface, meso- and bathypelagic clusters over large distances. The second aim of this study was to investigate the ecological significance of the crenarchaeotal nitrification in meso- and bathypelagic waters of the North Atlantic. Quantitative analyses of both archaeal and bacterial amoA genes (gene encoding for the ammonia monoxygenase alpha subunit) were performed to determine the ammonia oxidising bacterial and archaeal diversity in the deep waters of the North Atlantic. The archaeal amoA abundance was about one order of magnitude higher than that of bacterial nitrifiers, which are commonly thought to mediate the oxidation of ammonium to nitrite in marine environments. The analyses revealed that throughout the North Atlantic, the abundance of archaeal amoA genes decreases drastically from subsurface waters to 4000 m depth and from the subpolar to the equatorial deep waters leading to pronounced vertical and latitudinal gradients in the ratio of archaeal amoA to crenarchaeal 16S rRNA genes. This coincides with an increasing age of these waters masses and concomitantly, a decrease in the ammonia concentrations. Thus, only a minor fraction of the bathypelagic Crenarchaeota is putatively oxidising ammonia as energy source in the temperate and subtropical North Atlantic. This study suggests that, in the North Atlantic, bathypelagic Crenarchaeota are not autotrophic ammonia oxidisers but most likely utilise organic matter, hence live heterotrophically.

Data: CORDIS, © European Union

Project objective

This proposal is built on phylogenetic information on the prokaryotic communities of the coastal North Sea and in the open North Atlantic water. The sequence information available on the prokaryotic community will be used to construct oligonucleotide probe s for the main prokaryotic species present at these 2 sites. Using these fluorescent oligonucleotide probes in combination with the recently developed method catalysed reporter deposition-fluorescence in situ hybridisation (CARD-FISH), we will be able to determine the dynamics of the main components of the prokaryotic community. This CARD-FISH method is sensitive enough to allow detection of prokaryotic cells even in the deep ocean and will be combined with microautoradiography (MICRO-CARD-FISH).This combination of methods, recently developed in the host institution, allows the detection and enumeration of specific prokaryotic species and, at the same time, information is obtained on the utilization of specific compounds. Thus, the proposal directly addresses the functional biodiversity of marine prokaryotic plankton communities. MICRO-CARD-FISH will be used to determine the fluctuations in the activity of the main drivers of the prokaryotic succession in near-shore waters. Specific attention will be paid on the relation and activity pattern between Bacteria and Archaea, the 2 domains of the prokaryotes. Pelagic Archaea are not cultivable and their substrate requirements are unknown although they make up the majority of prokaryotic cells in the deep ocean water column and become numerically important in the North Sea in winter, when the number of Bacteria is low.Using MICRO-CARD-FISH, it has been shown that planktonic Archaea are capable of taking up bicarbonate or CO2 derived from it. The intention of the proposal is to decipher the dynamics of the main drivers of the carbon cycling in the prokaryotic community, thus focusing on a key component of the functional biodiversity in marine ecosystems.

Original text from CORDIS.

Participants

  • STICHTING KONINKLIJK NEDERLANDS INSTITUUT VOOR ONDERZOEK DER ZEE · DEN BURGCoordinatorCity levelNetherlands

Links

Data: CORDIS, © European Union