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Towards a palaeoecological model of the Mesoproterozoic Taoudeni Basin, Mauritania, Northwestern Africa: implications for early eukaryote evolution

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Geophysical Research Abstracts Vol. 18, EGU2016-5980, 2016 EGU General Assembly 2016

© Author(s) 2016. CC Attribution 3.0 License.

Towards a palaeoecological model of the Mesoproterozoic Taoudeni Basin,

Mauritania, Northwestern Africa: implications for early eukaryote

evolution

Jérémie Beghin (1), Romain Guilbaud (2), Simon W. Poulton (3), Nur Gueneli (4), Jochen J. Brocks (4), Jean-Yves Storme (1), Christian Blanpied (5), and Emmanuelle J. Javaux (1)

(1) University of Liège, Department of Geology, Liège, Belgium (jbeghin@ulg.ac.be), (2) University of Cambridge, Department of Earth Sciences, Cambridge, United Kingdom, (3) University of Leeds, School of Earth and Environment, Leeds, United Kingdom , (4) The Australian National University, Research School of Earth Sciences, Canberra, Australia, (5) TOTAL, Projets Nouveaux, Paris, France

The mid-Proterozoic rock record preserves a relatively moderate diversity of early eukaryotes, despite the early evolution of fundamental features of the eukaryotic cell. Common hypotheses involve the redox state of stratified oceans with oxic shallow waters, euxinic mid-depth waters, and anoxic and ferruginous deep waters during this time period. Mid-Proterozoic eukaryotes would have found suitable ecological niches in estuarine, fluvio-deltaic and coastal shallow marine environments near nutrient sources, while N2-fixing photoautotrophs bacteria would have been better competitors than eukaryotic algae in nutrient-poor niches.

Here, we present the first palaeoecological model of the late Mesoproterozoic Taoudeni Basin, Mauritania, Northwestern Africa. Previous palaeontological studies in the basin reported stromatolites, a low diversity of microfossils – including one species of presumed eukaryotes: verrucae-bearing acritarch – and biomarkers of anoxygenic phototrophic purple and green sulfur bacteria, cyanobacteria and microaerophilic methanotrophs. However, no biomarkers diagnostic for crown group eukaryotes were reported so far. In addition to exceptionally well preserved microbial mats showing chain-like aggregates of pyrite grains, we observed a total of sixty-two morphotaxa including nine presumed prokaryotes, thirty-five possible prokaryotes or eukaryotes, fifteen unam-biguous species of eukaryotes – ornamented and process-bearing acritarchs, multicellular morphotaxon, putative VSMs, large budding vesicles, and vesicles with a sophisticated excystment structure: the pylome – and three remains of structured kerogen.

Here, we combined the geological context (sedimentological features and lithofacies), iron speciation (n = 156) – with the aim of reconstructing palaeoredox environmental conditions –, and microfossils quantitative analysis (n = 61). Sediments were deposited under shallow waters in pericratonic (western basin) and epicratonic (eastern basin) marine environments during a depositional sequence linked to a marine transgression and regression. Both microfossil assemblages and iron speciation were analyzed on the same samples, with the aim of better understanding the palaeoecology of early eukaryotes.

Palaeoredox conditions rapidly fluctuated from oxic to anoxic states across the basin, but in terms of anoxic episodes, ferruginous conditions dominated in epicratonic environments, while euxinia was more prevalent in pericratonic environments. During the marine transgression, a relatively higher fossil eukaryotic diversity, both in terms of richness and abundance, was observed in the more proximal epicratonic environments while no eukaryotes were found in the more distal epicratonic environments; a relatively lower eukaryotic diversity was observed in pericratonic environments. After the marine regression, a relatively lower eukaryotic diversity was observed both in epicratonic and pericratonic environments. Our results could possibly suggest that both the availability of molecular oxygen and nutrients are needed for a high eukaryotic diversity and could confirm previous hypotheses suggesting that mid-Proterozoic eukaryotes would have found suitable ecological niches in shallow marine environments near nutrient sources.

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