ArticleEcology and evolution2016
A phylogenetic analysis of macroevolutionary patterns in fermentative yeasts.
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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Who cites it
7 citing papers in PubMed.
- Natural trait variation across Saccharomycotina species.FEMS yeast research · 2024Review
- Species-specific traits mediate avian demographic responses under past climate change.Nature ecology & evolution · 2023Article
- No escape: The influence of substrate sodium on plant growth and tissue sodium responses.Ecology and evolution · 2021Article
- Article
- Performance, genomic rearrangements, and signatures of adaptive evolution: Lessons from fermentative yeasts.Ecology and evolution · 2020Article
- Disentangling the role of floral sensory stimuli in pollination networks.Nature communications · 2018Article
- Macroevolutionary diversification of glands for chemical communication in squamate reptiles.Scientific reports · 2017Article
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
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.
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