Evidence map›Paper›PMID 29540154›Full record

ArticleBMC evolutionary biology2018

Anatomy of a Neotropical insect radiation.

Isaac Winkler, Sonja J Scheffer, Matthew L Lewis, Kristina J Ottens, Andrew P Rasmussen, Géssica A Gomes-Costa, Luz Maria Huerto Santillan, Marty A Condon, Andrew A Forbes

Abstract read
In one paragraph

Article in BMC evolutionary biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

9 authors.

Isaac WinklerDepartment of Biology, Cornell College, Mount Vernon, Iowa, 52314, USA. iwinkler@cornellcollege.edu.
Sonja J SchefferSystematic Entomology Laboratory, U.S. Department of Agriculture, Beltsville, MD, 20705, USA.
Matthew L LewisSystematic Entomology Laboratory, U.S. Department of Agriculture, Beltsville, MD, 20705, USA.
Kristina J OttensDepartment of Biology, University of Iowa, Iowa City, Iowa, 52242, USA.
Andrew P RasmussenDepartment of Biology, Cornell College, Mount Vernon, Iowa, 52314, USA.
Géssica A Gomes-CostaPrograma de Pós-Graduação em Biologia Vegetal, Universidade Federal de Pernambuco, Av. Prof°. Moraes Rego s/n, Cidade Universitária, Recife, Pernambuco, 50670-901, Brazil.
Luz Maria Huerto SantillanDepartamento de Entomología Museo de Historia Natural, Universidad Nacional Mayor de San Marcos, Av. Arenales 1256, Apartado 14-0434, 14, Lima, Peru.
Marty A CondonDepartment of Biology, Cornell College, Mount Vernon, Iowa, 52314, USA.
Andrew A ForbesDepartment of Biology, University of Iowa, Iowa City, Iowa, 52242, USA.

Funding

National Science Foundation DEB-0330845National Science Foundation DEB-0949361National Science Foundation DEB-1542269National Science Foundation DEB-1542451National Science Foundation HRD-9103322
6 · The paper itself

Abstract

backgroundMuch evolutionary theory predicts that diversity arises via both adaptive radiation (diversification driven by selection against niche-overlap within communities) and divergence of geographically isolated populations. We focus on tropical fruit flies (Blepharoneura, Tephritidae) that reveal unexpected patterns of niche-overlap within local communities. Throughout the Neotropics, multiple sympatric non-interbreeding populations often share the same highly specialized patterns of host use (e.g., flies are specialists on flowers of a single gender of a single species of host plants). Lineage through time (LTT) plots can help distinguish patterns of diversification consistent with ecologically limited adaptive radiation from those predicted by ecologically neutral theories. Here, we use a time-calibrated phylogeny of Blepharoneura to test the hypothesis that patterns of Blepharoneura diversification are consistent with an "ecologically neutral" model of diversification that predicts that diversification is primarily a function of time and space.

resultsThe Blepharoneura phylogeny showed more cladogenic divergence associated with geography than with shifts in host-use. Shifts in host-use were associated with ~ 20% of recent splits (< 3 Ma), but > 60% of older splits (> 3 Ma). In the overall tree, gamma statistic and maximum likelihood model fitting showed no evidence of diversification rate changes though there was a weak signature of slowing diversification rate in one of the component clades.

conclusionsOverall patterns of Blepharoneura diversity are inconsistent with a traditional explanation of adaptive radiation involving decreases in diversification rates associated with niche-overlap. Sister lineages usually use the same host-species and host-parts, and multiple non-interbreeding sympatric populations regularly co-occur on the same hosts. We suggest that most lineage origins (phylogenetic splits) occur in allopatry, usually without shifts in host-use, and that subsequent dispersal results in assembly of communities composed of multiple sympatric non-interbreeding populations of flies that share the same hosts.

Indexed as

AnimalsBiodiversityBiological EvolutionEcologyFlowersGenetic SpeciationGeographyHerbivoryLikelihood FunctionsPhylogenyPlantsSympatryTephritidaeDiversificationHerbivorous insectsHost-useLineage through time (LTT) plotsNeutral theoryParasitoidsSpeciationTropics

Identifiers

PMID29540154
PMCPMC5853117

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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.