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Morphological stasis in the first myxomycete from the Mesozoic, and the likely role of cryptobiosis

Myxomycetes constitute a group within the Amoebozoa well known for their motile plasmodia and morphologically complex fruiting bodies. One obstacle hindering studies of myxomycete evolution is that their fossils are exceedingly rare, so evolutionary analyses of this supposedly ancient lineage of amo...

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Autores principales: Rikkinen, Jouko, Grimaldi, David A., Schmidt, Alexander R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6930221/
https://www.ncbi.nlm.nih.gov/pubmed/31874965
http://dx.doi.org/10.1038/s41598-019-55622-9
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author Rikkinen, Jouko
Grimaldi, David A.
Schmidt, Alexander R.
author_facet Rikkinen, Jouko
Grimaldi, David A.
Schmidt, Alexander R.
author_sort Rikkinen, Jouko
collection PubMed
description Myxomycetes constitute a group within the Amoebozoa well known for their motile plasmodia and morphologically complex fruiting bodies. One obstacle hindering studies of myxomycete evolution is that their fossils are exceedingly rare, so evolutionary analyses of this supposedly ancient lineage of amoebozoans are restricted to extant taxa. Molecular data have significantly advanced myxomycete systematics, but the evolutionary history of individual lineages and their ecological adaptations remain unknown. Here, we report exquisitely preserved myxomycete sporocarps in amber from Myanmar, ca. 100 million years old, one of the few fossil myxomycetes, and the only definitive Mesozoic one. Six densely-arranged stalked sporocarps were engulfed in tree resin while young, with almost the entire spore mass still inside the sporotheca. All morphological features are indistinguishable from those of the modern, cosmopolitan genus Stemonitis, demonstrating that sporocarp morphology has been static since at least the mid-Cretaceous. The ability of myxomycetes to develop into dormant stages, which can last years, may account for the phenotypic stasis between living Stemonitis species and this fossil one, similar to the situation found in other organisms that have cryptobiosis. We also interpret Stemonitis morphological stasis as evidence of strong environmental selection favouring the maintenance of adaptations that promote wind dispersal.
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spelling pubmed-69302212019-12-27 Morphological stasis in the first myxomycete from the Mesozoic, and the likely role of cryptobiosis Rikkinen, Jouko Grimaldi, David A. Schmidt, Alexander R. Sci Rep Article Myxomycetes constitute a group within the Amoebozoa well known for their motile plasmodia and morphologically complex fruiting bodies. One obstacle hindering studies of myxomycete evolution is that their fossils are exceedingly rare, so evolutionary analyses of this supposedly ancient lineage of amoebozoans are restricted to extant taxa. Molecular data have significantly advanced myxomycete systematics, but the evolutionary history of individual lineages and their ecological adaptations remain unknown. Here, we report exquisitely preserved myxomycete sporocarps in amber from Myanmar, ca. 100 million years old, one of the few fossil myxomycetes, and the only definitive Mesozoic one. Six densely-arranged stalked sporocarps were engulfed in tree resin while young, with almost the entire spore mass still inside the sporotheca. All morphological features are indistinguishable from those of the modern, cosmopolitan genus Stemonitis, demonstrating that sporocarp morphology has been static since at least the mid-Cretaceous. The ability of myxomycetes to develop into dormant stages, which can last years, may account for the phenotypic stasis between living Stemonitis species and this fossil one, similar to the situation found in other organisms that have cryptobiosis. We also interpret Stemonitis morphological stasis as evidence of strong environmental selection favouring the maintenance of adaptations that promote wind dispersal. Nature Publishing Group UK 2019-12-24 /pmc/articles/PMC6930221/ /pubmed/31874965 http://dx.doi.org/10.1038/s41598-019-55622-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Rikkinen, Jouko
Grimaldi, David A.
Schmidt, Alexander R.
Morphological stasis in the first myxomycete from the Mesozoic, and the likely role of cryptobiosis
title Morphological stasis in the first myxomycete from the Mesozoic, and the likely role of cryptobiosis
title_full Morphological stasis in the first myxomycete from the Mesozoic, and the likely role of cryptobiosis
title_fullStr Morphological stasis in the first myxomycete from the Mesozoic, and the likely role of cryptobiosis
title_full_unstemmed Morphological stasis in the first myxomycete from the Mesozoic, and the likely role of cryptobiosis
title_short Morphological stasis in the first myxomycete from the Mesozoic, and the likely role of cryptobiosis
title_sort morphological stasis in the first myxomycete from the mesozoic, and the likely role of cryptobiosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6930221/
https://www.ncbi.nlm.nih.gov/pubmed/31874965
http://dx.doi.org/10.1038/s41598-019-55622-9
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