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The evolution of multicellular life spurred evolutionary radiations, fundamentally changing many of Earth’s ecosystems. Yet little is known about how early steps in the evolution of multicellularity affect eco-evolutionary dynamics. Through long-term experimental evolution, we observed niche partitioning and the adaptive divergence of two specialized lineages from a single multicellular ancestor. Over 715 daily transfers, snowflake yeast were subjected to selection for rapid growth, followed by selection favouring larger group size. Small and large cluster-forming lineages evolved from a monomorphic ancestor, coexisting for over ~4,300 generations, specializing on divergent aspects of a trade-off between growth rate and survival. Through modelling and experimentation, we demonstrate that coexistence is maintained by a trade-off between organismal size and competitiveness for dissolved oxygen. Taken together, this work shows how the evolution of a new level of biological individuality can rapidly drive adaptive diversification and the expansion of a nascent multicellular niche, one of the most historically impactful emergent properties of this evolutionary transition.
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Adaptive radiation during the evolution of complex multicellularity
Abstract The evolution of multicellularity led to the origin of new kinds of organisms and, in several lineages, massive adaptive radiations through the formation of entirely new ecosystems. This paper examines three key mechanisms underpinning parallel adaptive radiations within the five clades of ‘complex’ multicellularity: animals, land plants, fungi, red algae, and brown algae. First, the evolution of key multicellular innovations permitted diversification into new ecological roles. Second, the evolution of large multicellular organisms with strong genetic bottlenecks between generations fundamentally changed the population genetic context of evolution, greatly reducing effective population size and increasing the role of genetic drift. This may be beneficial during adaptive radiations, underpinning nonadaptive expansions of genome size and allowing broader exploration of multicellular trait space. Finally, we explore how evolutionary priority effects provide a first-mover advantage, maintaining ancient adaptive radiations over long time periods by suppressing competition from convergently evolving multicellular taxa. Investigating parallel patterns of diversification across independent origins of complex multicellularity provides insight into the principles underpinning these crucially important adaptive radiations.
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- PAR ID:
- 10526939
- Publisher / Repository:
- Oxford University Press
- Date Published:
- Journal Name:
- Evolutionary Journal of the Linnean Society
- Volume:
- 3
- Issue:
- 1
- ISSN:
- 2752-938X
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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