Evidence map›Paper›PMID 27374779›Full record

ArticleJournal of evolutionary biology2016

Ecological speciation in sympatric palms: 2. Pre- and post-zygotic isolation.

H Hipperson, L T Dunning, W J Baker, R K Butlin, I Hutton, A S T Papadopulos, C M Smadja, T C Wilson, C Devaux, V Savolainen

Open access · hybridAbstract read
In one paragraph

Article in Journal of evolutionary biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
11.4field-weighted citation impact, top 2% of its field
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

5 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Sympatric speciation in mountain roses (Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Article
  4. Article
  5. 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

10 authors at 5 institutions in 4 countries.

H HippersonDepartment of Life Sciences, Imperial College London, Silwood Park Campus, Ascot, UK.
L T DunningDepartment of Life Sciences, Imperial College London, Silwood Park Campus, Ascot, UK.
W J BakerRoyal Botanic Gardens, Kew, Richmond, UK.
R K ButlinDepartment of Animal and Plant Sciences, University of Sheffield, Sheffield, UK.
I HuttonLord Howe Island Museum, Lord Howe Island, NSW, Australia.
A S T PapadopulosDepartment of Life Sciences, Imperial College London, Silwood Park Campus, Ascot, UK.ORCID 0000-0001-6589-754X
C M SmadjaDepartment of Life Sciences, Imperial College London, Silwood Park Campus, Ascot, UK.
T C WilsonRoyal Botanic Gardens and Domain Trust, Sydney, NSW, Australia.
C Devaux
V SavolainenDepartment of Life Sciences, Imperial College London, Silwood Park Campus, Ascot, UK. v.savolainen@imperial.ac.uk.
Imperial College London · GBRoyal Botanic Gardens, Kew · GBInstitut des Sciences de l'Evolution de Montpellier · FRRoyal Botanic Garden Sydney · AUUniversity of Gothenburg · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We evaluated reproductive isolation in two species of palms (Howea) that have evolved sympatrically on Lord Howe Island (LHI, Australia). We estimated the strength of some pre- and post-zygotic mechanisms in maintaining current species boundaries. We found that flowering time displacement between species is consistent across in and ex situ common gardens and is thus partly genetically determined. On LHI, pre-zygotic isolation due solely to flowering displacement was 97% for Howea belmoreana and 80% for H. forsteriana; this asymmetry results from H. forsteriana flowering earlier than H. belmoreana and being protandrous. As expected, only a few hybrids (here confirmed by genotyping) at both juvenile and adult stages could be detected in two sites on LHI, in which the two species grow intermingled (the Far Flats) or adjacently (Transit Hill). Yet, the distribution of hybrids was different between sites. At Transit Hill, we found no hybrid adult trees, but 13.5% of younger palms examined there were of late hybrid classes. In contrast, we found four hybrid adult trees, mostly of late hybrid classes, and only one juvenile F1 hybrid in the Far Flats. This pattern indicates that selection acts against hybrids between the juvenile and adult stages. An in situ reciprocal seed transplant between volcanic and calcareous soils also shows that early fitness components (up to 36 months) were affected by species and soil. These results are indicative of divergent selection in reproductive isolation, although it does not solely explain the current distribution of the two species on LHI.

Indexed as

ArecaceaeHybridization, GeneticReproductive IsolationSympatryAnimalsAustraliaGenotypefloweringhybridizationphenologypost-zygoticpre-zygotic

Identifiers

PMID27374779
PMCPMC5096058
OpenAlexW2468467192

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.