A precise relationship among Buller's drop, ballistospore, and gill morphologies enables maximum packing of spores within gilled mushrooms.

Ballistospory biomechanics fungi morphometrics

Journal

Mycologia
ISSN: 1557-2536
Titre abrégé: Mycologia
Pays: England
ID NLM: 0400764

Informations de publication

Date de publication:
Historique:
pubmed: 27 1 2021
medline: 23 9 2021
entrez: 26 1 2021
Statut: ppublish

Résumé

Basidiomycete fungi eject basidiospores using a surface tension catapult. A fluid drop forms at the base of each spore and, after reaching a critical size, coalesces with the spore and launches it from the gill surface. It has long been hypothesized that basidiomycete fungi pack the maximum number of spores into a minimal investment of biomass. Building on a nascent understanding of the physics underpinning the surface tension catapult, we modeled a spore's trajectory away from a basidium and demonstrated that to achieve maximum packing the size of the fluid drop, the size of the spore, and the distance between gills must be finely coordinated. To compare the model with data, we measured spore and gill morphologies from wild mushrooms and compared measurements with the model. The empirical data suggest that in order to pack the maximum number of spores into the least amount of biomass, the size of Buller's drop should be smaller but comparable to the spore size. Previously published data of Buller's drop and spore sizes support our hypothesis and also suggest a linear scaling between spore radius and Buller's drop radius. Morphological features of the surface tension catapult appear tightly regulated to enable maximum packing of spores. If mushrooms are maximally packed and Buller's drop radii scale linearly with spore radii, we predict that intergill distance should be proportional to spore radius to the power 3/2.

Identifiants

pubmed: 33497296
doi: 10.1080/00275514.2020.1823175
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

300-311

Auteurs

Martina Iapichino (M)

Institut de Physique de Nice, UMR7010, Centre National de la Recherche Scientifique (CNRS) and Université Côte d'Azur, Nice, France.

Yen-Wen Wang (YW)

Department of Botany, University of Wisconsin-Madison, Madison, Wisconsin 53706.
Department of Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin 53706.

Savannah Gentry (S)

Department of Botany, University of Wisconsin-Madison, Madison, Wisconsin 53706.
Department of Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin 53706.

Anne Pringle (A)

Department of Botany, University of Wisconsin-Madison, Madison, Wisconsin 53706.
Department of Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin 53706.

Agnese Seminara (A)

Institut de Physique de Nice, UMR7010, Centre National de la Recherche Scientifique (CNRS) and Université Côte d'Azur, Nice, France.

Articles similaires

Meiosis Schizosaccharomyces Schizosaccharomyces pombe Proteins Spores, Fungal

Emergence of synchronized growth oscillations in filamentous fungi.

Praneet Prakash, Xue Jiang, Luke Richards et al.
1.00
Models, Biological Spores, Fungal Basidiomycota Fungi
Alternaria Temperature Spores, Fungal Water Germination
Bibliometrics Agaricales China Research Agriculture

Classifications MeSH