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Amoebozoan testate amoebae illuminate the diversity of heterotrophs and the complexity of ecosystems throughout geological time

Proceedings of the National Academy of Sciences of the United States of America. Bd. 121. H. 30. Washington, DC: National Academy of Sciences 2024

Erscheinungsjahr: 2024

ISBN/ISSN: 1091-6490

Publikationstyp: Zeitschriftenaufsatz

Sprache: Englisch

Doi/URN: 10.1073/pnas.2319628121

Volltext über DOI/URN

Geprüft:Bibliothek

Inhaltszusammenfassung


Arcellinida shelled amoebae are heterotrophic microbial eukaryotes with an extensive Neoproterozoic fossil record, the vase-shaped microfossils (VSMs), a diverse group that is abundant and widespread in late Tonian rocks. We combined phylogenomic sampling and the fossil record to generate time-calibrated trees. Our results illuminate key events in the history of life, including: i) the Tonian origin of extant microbial eukaryote lineages; ii) a speculative proposed radiation of eukaryotes bef...Arcellinida shelled amoebae are heterotrophic microbial eukaryotes with an extensive Neoproterozoic fossil record, the vase-shaped microfossils (VSMs), a diverse group that is abundant and widespread in late Tonian rocks. We combined phylogenomic sampling and the fossil record to generate time-calibrated trees. Our results illuminate key events in the history of life, including: i) the Tonian origin of extant microbial eukaryote lineages; ii) a speculative proposed radiation of eukaryotes before the Cryogenian, “Tonian revolution”; iii) the establishment of complex terrestrial habitats before the Cryogenian; iv) a post-Silurian divergence of modern Arcellinida subclades in terrestrial (including freshwater) habitats. Our results provide insights into the evolution of life throughout geological time and are congruent with recent discoveries regarding the early diversification of eukaryotes. Heterotrophic protists are vital in Earth’s ecosystems, influencing carbon and nutrient cycles and occupying key positions in food webs as microbial predators. Fossils and molecular data suggest the emergence of predatory microeukaryotes and the transition to a eukaryote-rich marine environment by 800 million years ago (Ma). Neoproterozoic vase-shaped microfossils (VSMs) linked to Arcellinida testate amoebae represent the oldest evidence of heterotrophic microeukaryotes. This study explores the phylogenetic relationship and divergence times of modern Arcellinida and related taxa using a relaxed molecular clock approach. We estimate the origin of nodes leading to extant members of the Arcellinida Order to have happened during the latest Mesoproterozoic and Neoproterozoic (1054 to 661 Ma), while the divergence of extant infraorders postdates the Silurian. Our results demonstrate that at least one major heterotrophic eukaryote lineage originated during the Neoproterozoic. A putative radiation of eukaryotic groups (e.g., Arcellinida) during the early-Neoproterozoic sustained by favorable ecological and environmental conditions may have contributed to eukaryotic life endurance during the Cryogenian severe ice ages. Moreover, we infer that Arcellinida most likely already inhabited terrestrial habitats during the Neoproterozoic, coexisting with terrestrial Fungi and green algae, before land plant radiation. The most recent extant Arcellinida groups diverged during the Silurian Period, alongside other taxa within Fungi and flowering plants. These findings shed light on heterotrophic microeukaryotes’ evolutionary history and ecological significance in Earth’s ecosystems, using testate amoebae as a proxy.» weiterlesen» einklappen

  • Arcellinida
  • ancestral state reconstruction
  • eukaryotic evolution
  • phylogenomics
  • vase-shaped microfossils

Autoren


Porfirio-Sousa, Alfredo L. (Autor)
Tice, Alexander K. (Autor)
Morais, Luana (Autor)
Ribeiro, Giulia M. (Autor)
Blandenier, Quentin (Autor)
Dumack, Kenneth (Autor)
Eglit, Yana (Autor)
Fry, Nicholas W. (Autor)
Souza, Maria Beatriz Gomes E (Autor)
Henderson, Tristan C. (Autor)
Kleitz-Singleton, Felicity (Autor)
Singer, David (Autor)
Brown, Matthew W. (Autor)
Lahr, Daniel J. G. (Autor)