Evidence map›Paper›PMID 27516851›Full record

ArticleEcology and evolution2016

A phylogenetic analysis of macroevolutionary patterns in fermentative yeasts.

Rocío Paleo-López, Julian F Quintero-Galvis, Jaiber J Solano-Iguaran, Angela M Sanchez-Salazar, Juan D Gaitan-Espitia, Roberto F Nespolo

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Article in Ecology and evolution, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

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7citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Rocío Paleo-LópezInstituto de Ciencias Ambientales y Evolutivas Universidad Austral de Chile Valdivia 5090000 Chile.
Julian F Quintero-GalvisInstituto de Ciencias Ambientales y Evolutivas Universidad Austral de Chile Valdivia 5090000 Chile.
Jaiber J Solano-IguaranInstituto de Ciencias Ambientales y Evolutivas Universidad Austral de Chile Valdivia 5090000 Chile.
Angela M Sanchez-SalazarInstituto de Ciencias Ambientales y Evolutivas Universidad Austral de Chile Valdivia 5090000 Chile.
Juan D Gaitan-EspitiaInstituto de Ciencias Ambientales y Evolutivas Universidad Austral de Chile Valdivia 5090000 Chile; CSIRO Oceans & Atmosphere GPO Box 1538 Hobart 7001 Tasmania Australia.
Roberto F NespoloInstituto de Ciencias Ambientales y Evolutivas Universidad Austral de Chile Valdivia 5090000 Chile; Center of Applied Ecology and Sustainability (CAPES) Facultad de Ciencias Biológicas Universidad Católica de Chile Santiago 6513677 Chile.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

When novel sources of ecological opportunity are available, physiological innovations can trigger adaptive radiations. This could be the case of yeasts (Saccharomycotina), in which an evolutionary novelty is represented by the capacity to exploit simple sugars from fruits (fermentation). During adaptive radiations, diversification and morphological evolution are predicted to slow-down after early bursts of diversification. Here, we performed the first comparative phylogenetic analysis in yeasts, testing the "early burst" prediction on species diversification and also on traits of putative ecological relevance (cell-size and fermentation versatility). We found that speciation rates are constant during the time-range we considered (ca., 150 millions of years). Phylogenetic signal of both traits was significant (but lower for cell-size), suggesting that lineages resemble each other in trait-values. Disparity analysis suggested accelerated evolution (diversification in trait values above Brownian Motion expectations) in cell-size. We also found a significant phylogenetic regression between cell-size and fermentation versatility (R (2) = 0.10), which suggests correlated evolution between both traits. Overall, our results do not support the early burst prediction both in species and traits, but suggest a number of interesting evolutionary patterns, that warrant further exploration. For instance, we show that the Whole Genomic Duplication that affected a whole clade of yeasts, does not seems to have a statistically detectable phenotypic effect at our level of analysis. In this regard, further studies of fermentation under common-garden conditions combined with comparative analyses are warranted.

Indexed as

Adaptive radiationcomparative methodfermentationphylogenetic signalSaccharomicotina

Identifiers

PMID27516851
PMCPMC4972215

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.