Evidence map›Paper›PMID 32406164›Full record

ArticlePest management science2020

Geographic variation in sexual communication in the cotton bollworm, Helicoverpa armigera.

Ke Gao, Luis M Torres-Vila, Myron P Zalucki, Yiping Li, Frans Griepink, David G Heckel, Astrid T Groot

Open access · hybridAbstract read
In one paragraph

Article in Pest management science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

2 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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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

7 authors at 4 institutions in 4 countries.

Ke GaoInstitute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0003-3006-7073
Luis M Torres-VilaServicio de Sanidad Vegetal, Consejería de Medio Ambiente y Rural PAyT, Badajoz, Spain.
Myron P ZaluckiSchool of Biological Science, The University of Queensland, Brisbane, Australia.
Yiping LiKey Laboratory of Plant Protection Resources and Pest Management, Ministry of Education, Northwest A&F University, Yangling, China.ORCID https://orcid.org/0000-0002-9461-813X
Frans GriepinkPherobank BV, Wijk bij Duurstede, The Netherlands.
David G HeckelMax Planck Institute for Chemical Ecology, Department of Entomology, Jena, Germany.
Astrid T GrootInstitute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam, The Netherlands.
Max Planck Institute for Chemical Ecology · DEMinistry of Education of the People's Republic of China · CNQueensland University of Technology · AUUniversity of Amsterdam · NL

Funding

China Scholarship Council 201506300162Netherlands Organisation for Scientific Research 822.01.012the Max-Planck-Gesellschaftthe National Science Foundation IOS-1456973
6 · The paper itself

Abstract

backgroundGeographic variation in male response to sex pheromone lures has been studied in the field in a number of moth species. However, only a few studies have investigated geographic variation in female calling and sex pheromone under field conditions. For an effective field implementation of sex pheromone lures, it is essential to know the local sex pheromone blend and local timing of sexual communication. We investigated the level and extent of geographic variation in the sexual communication of the important agricultural pest Helicoverpa armigera (Lepidoptera, Noctuidae) in three continents.

resultsWe found there is no genetic variation in the calling behavior of H. armigera. In the female sex pheromone, we found more between-population variation than within-population variation. In male response experiments, we found geographic variation as well. Strikingly, when adding the antagonistic compound Z11-16:OAc to the pheromone blend of H. armigera, significantly fewer males were caught in Australia and China, but not in Spain. This variation is likely not only due to local environmental conditions, such as photoperiod and temperature, but also to the presence of other closely related species with which communication interference may occur.

conclusionFinding geographic variation in both the female sexual signal and the male response in this pest calls for region-specific pheromone lures. Our study shows that the analysis of geographic variation in moth female sex pheromones as well as male responses is important for effectively monitoring pest species that occur around the globe. © 2020 The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

Indexed as

MothsAnimalsAustraliaChinaFemaleMaleSex AttractantsSpainSex Attractantscommunication interferencecotton bollwormsex pheromonesexual behavior

Identifiers

PMID32406164
PMCPMC7586828
OpenAlexW3025775003

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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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.