Evolution of fungal phenotypic disparity

Organismal-grade multicellularity has been achieved only in animals, plants and fungi. All three kingdoms manifest phenotypically disparate body plans but their evolution has only been considered in detail for animals. Here we tested the general relevance of hypotheses on the evolutionary assembly o...

Descrizione completa

Dettagli Bibliografici
Autori principali: Smith, TJ, Donoghue, PCJ
Natura: Journal article
Lingua:English
Pubblicazione: Springer Nature 2022
_version_ 1826310510972239872
author Smith, TJ
Donoghue, PCJ
author_facet Smith, TJ
Donoghue, PCJ
author_sort Smith, TJ
collection OXFORD
description Organismal-grade multicellularity has been achieved only in animals, plants and fungi. All three kingdoms manifest phenotypically disparate body plans but their evolution has only been considered in detail for animals. Here we tested the general relevance of hypotheses on the evolutionary assembly of animal body plans by characterizing the evolution of fungal phenotypic variety (disparity). The distribution of living fungal form is defined by four distinct morphotypes: flagellated; zygomycetous; sac-bearing; and club-bearing. The discontinuity between morphotypes is a consequence of extinction, indicating that a complete record of fungal disparity would present a more homogeneous distribution of form. Fungal disparity expands episodically through time, punctuated by a sharp increase associated with the emergence of multicellular body plans. Simulations show these temporal trends to be non-random and at least partially shaped by hierarchical contingency. These trends are decoupled from changes in gene number, genome size and taxonomic diversity. Only differences in organismal complexity, characterized as the number of traits that constitute an organism, exhibit a meaningful relationship with fungal disparity. Both animals and fungi exhibit episodic increases in disparity through time, resulting in distributions of form made discontinuous by extinction. These congruences suggest a common mode of multicellular body plan evolution.
first_indexed 2024-03-07T07:53:05Z
format Journal article
id oxford-uuid:7459fa3b-df9c-4171-afa1-9ff1917c0255
institution University of Oxford
language English
last_indexed 2024-03-07T07:53:05Z
publishDate 2022
publisher Springer Nature
record_format dspace
spelling oxford-uuid:7459fa3b-df9c-4171-afa1-9ff1917c02552023-08-01T11:09:20ZEvolution of fungal phenotypic disparityJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:7459fa3b-df9c-4171-afa1-9ff1917c0255EnglishSymplectic ElementsSpringer Nature2022Smith, TJDonoghue, PCJOrganismal-grade multicellularity has been achieved only in animals, plants and fungi. All three kingdoms manifest phenotypically disparate body plans but their evolution has only been considered in detail for animals. Here we tested the general relevance of hypotheses on the evolutionary assembly of animal body plans by characterizing the evolution of fungal phenotypic variety (disparity). The distribution of living fungal form is defined by four distinct morphotypes: flagellated; zygomycetous; sac-bearing; and club-bearing. The discontinuity between morphotypes is a consequence of extinction, indicating that a complete record of fungal disparity would present a more homogeneous distribution of form. Fungal disparity expands episodically through time, punctuated by a sharp increase associated with the emergence of multicellular body plans. Simulations show these temporal trends to be non-random and at least partially shaped by hierarchical contingency. These trends are decoupled from changes in gene number, genome size and taxonomic diversity. Only differences in organismal complexity, characterized as the number of traits that constitute an organism, exhibit a meaningful relationship with fungal disparity. Both animals and fungi exhibit episodic increases in disparity through time, resulting in distributions of form made discontinuous by extinction. These congruences suggest a common mode of multicellular body plan evolution.
spellingShingle Smith, TJ
Donoghue, PCJ
Evolution of fungal phenotypic disparity
title Evolution of fungal phenotypic disparity
title_full Evolution of fungal phenotypic disparity
title_fullStr Evolution of fungal phenotypic disparity
title_full_unstemmed Evolution of fungal phenotypic disparity
title_short Evolution of fungal phenotypic disparity
title_sort evolution of fungal phenotypic disparity
work_keys_str_mv AT smithtj evolutionoffungalphenotypicdisparity
AT donoghuepcj evolutionoffungalphenotypicdisparity