4.7 Review

A unifying, eco-physiological framework for animal dormancy

Journal

FUNCTIONAL ECOLOGY
Volume 35, Issue 1, Pages 11-31

Publisher

WILEY
DOI: 10.1111/1365-2435.13718

Keywords

diapause; hibernation; hypometabolism; metabolic suppression; seasonality; torpor; winter

Categories

Funding

  1. NSF Division of Graduate Education [1106400]
  2. NSF Division of Integrative Organismal Systems [1558159]
  3. NSF Division of Biological Infrastructure [1907233]
  4. Direct For Biological Sciences [1558159] Funding Source: National Science Foundation
  5. Direct For Biological Sciences
  6. Div Of Biological Infrastructure [1907233] Funding Source: National Science Foundation
  7. Division Of Integrative Organismal Systems [1558159] Funding Source: National Science Foundation

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Animals across different taxonomic groups exhibit similar phenotypes during programmed dormancy in highly seasonal environments, but research on dormancy has been historically limited by phylogenetic barriers. A broad comparative approach could provide new insights into the evolution of programmed dormancy.
Various animals across the tree of life express some form of programmed dormancy (e.g. hibernation, diapause) to maximize fitness in highly seasonal environments. The integrated phenotype of animals undergoing programmed dormancy is strikingly similar among diverse groups; however, research on programmed dormancy has historically been phylogenetically siloed. A broad comparative approach could clarify new angles for answering fundamental questions about programmed dormancy evolution. To advance this approach, we present a cross-taxonomic framework describing dimensions that distinguish animal dormancies and provide a set of core traits that animals regulate as they progress through the eco-physiological phases of deep, programmed dormancy. We use this universal framework to explore the ultimate drivers and evolutionary consequences of dormancy across the tree of life. Deep, programmed dormancy appears to be a predictable and repeated adaptation to highly seasonal environments that draws on a conserved suite of ancestral traits. We highlight evidence for molecular convergence in signalling pathways coordinating environmental sensing and energy metabolism in the insect and mammal lineages, separated by 700 million years of evolution and representing independent colonizations of highly seasonal environments. Lastly, we discuss the utility of this new framework and highlight opportunities and challenges for researchers to continue advancing our understanding of dormancy through a broad, comparative lens. A free Plain Language Summary can be found within the Supporting Information of this article.

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