Evidence map›Paper›PMID 33135108›Full record

ArticleJournal of chemical ecology2021

Identification of Zingiberenol and Murgantiol as Components of the Aggregation-Sex Pheromone of the Rice Stink Bug, Mormidea v-luteum (Heteroptera: Pentatomidae).

Antonioni Acacio Campos Moliterno, Douglas José De Melo, Paulo Henrique Gorgatti Zarbin

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Article in Journal of chemical ecology, 2021. 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

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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. 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

3 authors.

Antonioni Acacio Campos MoliternoDepartamento de Química, Universidade Federal do Paraná, Caixa Postal 19081, Curitiba, PR, 81531-990, Brazil.
Douglas José De MeloDepartamento de Química, Universidade Federal do Paraná, Caixa Postal 19081, Curitiba, PR, 81531-990, Brazil.
Paulo Henrique Gorgatti ZarbinDepartamento de Química, Universidade Federal do Paraná, Caixa Postal 19081, Curitiba, PR, 81531-990, Brazil. pzarbin@ufpr.br.ORCID http://orcid.org/0000-0001-6485-7642

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 310258/2017-0
6 · The paper itself

Abstract

Mormidea v-luteum (Lichtenstein, 1796) feeds on commercial crops, such as rice and ryegrass, causing damage that slows growth and reduces productivity. With the aim of developing an eco-friendly control technique, we investigated the compounds involved in chemical communication in this species. The volatiles produced by a group of seven males or females allocated to different aerated glass chambers were collected for 24 h and analyzed by gas chromatograph/mass spectrometry and gas chromatography/Fourier transform infrared spectroscopy. The analyses showed six male-specific compounds, identified as two isomers of zingiberenol (compounds 1 and 2), three isomers of murgantiol (3, 5 and 6) and sesquipiperitol (4). Compounds 1 and 5 were the major components and were produced in a ratio of 6:4. The absolute stereochemistry of the two isomers of zingiberenol was established as (1S,4R,1'S)-1 and (1R,4R,1'S)-2 by chiral gas chromatography. Stereochemistry was not determined for all the other molecules. To confirm the attractiveness of these chemicals, bioassays were performed in a Y-tube olfactometer, first using crude extracts and, subsequently, synthetic compounds. Male volatiles were attractive to both sexes, demonstrating an aggregation pheromone. In bioassays with synthetic compounds, (1'S)-zingiberenol was highly attractive to both males and females. However, when (1'S)-murgantiol was tested, only females were attracted. Interestingly, when a mixture of zingiberenol and murgantiol isomers was tested, it was attractive to both sexes, with females more attracted to the mixture than to zingiberenol alone; males did not distinguish between treatments. Thus, the bioassay data suggest that the molecules have different functions in chemical communication of this species: zingiberenol acts primarily as an aggregation pheromone, while murgantiol plays a role as a sex pheromone.

Indexed as

AnimalsFemaleHeteropteraMaleOlfactometrySesquiterpenesSex Attractants4-(3-(3,3-dimethyloxiran-2-yl)-1-methylpropyl)-1-methylcyclohex-2-en-1olSesquiterpenesSex AttractantszingiberenolMurgantiolPentatomidaeSesquipiperitolSex-specific compoundsZingiberenol

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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.