Evidence map›Paper›PMID 28894101›Full record

ArticleScientific reports2017

Intense natural selection preceded the invasion of new adaptive zones during the radiation of New World leaf-nosed bats.

Daniela M Rossoni, Ana Paula A Assis, Norberto P Giannini, Gabriel Marroig

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Article
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  8. Making a bat: The developmental basis of bat evolution.Genetics and molecular biology · 2021
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  13. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Daniela M RossoniDepartment of Genetics and Evolutionary Biology, Biosciences Institute, University of São Paulo, Rua do Matão, 277, 05508-900, São Paulo, Brazil. daniela.rossoni@usp.br.
Ana Paula A AssisDepartment of Ecology, Biosciences Institute, University of São Paulo, Rua do Matão, 277, 05508-900, São Paulo, Brazil.
Norberto P GianniniUnidad Ejecutora Lillo-CONICET, Miguel Lillo 251, Universidad Nacional de Tucumán, Tucumán, 4000, Argentina.
Gabriel MarroigDepartment of Genetics and Evolutionary Biology, Biosciences Institute, University of São Paulo, Rua do Matão, 277, 05508-900, São Paulo, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The family Phyllostomidae, which evolved in the New World during the last 30 million years, represents one of the largest and most morphologically diverse mammal families. Due to its uniquely diverse functional morphology, the phyllostomid skull is presumed to have evolved under strong directional selection; however, quantitative estimation of the strength of selection in this extraordinary lineage has not been reported. Here, we used comparative quantitative genetics approaches to elucidate the processes that drove cranial evolution in phyllostomids. We also quantified the strength of selection and explored its association with dietary transitions and specialization along the phyllostomid phylogeny. Our results suggest that natural selection was the evolutionary process responsible for cranial diversification in phyllostomid bats. Remarkably, the strongest selection in the phyllostomid phylogeny was associated with dietary specialization and the origination of novel feeding habits, suggesting that the adaptive diversification of phyllostomid bats was triggered by ecological opportunities. These findings are consistent with Simpson's quantum evolutionary model of transitions between adaptive zones. The multivariate analyses used in this study provides a powerful tool for understanding the role of evolutionary processes in shaping phenotypic diversity in any group on both micro- and macroevolutionary scales.

Indexed as

Biological EvolutionChiropteraRadiationSelection, GeneticAnimalsBiodiversityCluster AnalysisEnvironment

Identifiers

PMID28894101
PMCPMC5593990

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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.