Evidence map›Paper›PMID 39904809›Full record

ArticleJournal of chemical ecology2025

Sex Pheromone of the Papaya Mealybug.

Yuma Sugawara, Takumi Uesato, Jun Tabata

Abstract read
In one paragraph

Article in Journal of chemical ecology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Yuma SugawaraDivision of Fruit Tree and Tea Pest Control Research, Institute for Plant Protection, National Agriculture and Food Research Organization, 301-2 Akitsu, Higashi-Hiroshima, Hiroshima, 739‑2494, Japan.
Takumi UesatoDepartment of Agriculture, Forestry and Fisheries, Okinawa Prefecture, Okinawa Prefectural Plant Protection Center, 123 Maji, Naha, Okinawa, 901-0072, Japan.
Jun TabataDivision of Core Technology for Pest Control Research, Institute for Plant Protection, National Agriculture and Food Research Organization, 3‑1‑3 Kannondai, Tsukuba, Ibaraki, 305‑8604, Japan. tabata.jun.gn@u.tsukuba.ac.jp.

Funding

Japan Society for the Promotion of Science 21K05628
6 · The paper itself

Abstract

Sex pheromones of mealybugs are reported from more than 20 species and have generally been shown to be monoterpene alcohols esterified with short-chain carboxylic acids. Here, however, we discovered and isolated an alcohol without an acid moiety as a pheromone compound released from adult females of the papaya mealybug, Paracoccus marginatus. By means of gas chromatography - mass spectrometry and nuclear magnetic resonance spectroscopy analyses, the structure was identified to be trans-2-(2-isopropenyl-1-methylcyclobutyl)ethanol, a monoterpene with a unique cyclobutene skeleton, commonly known as fragranol. We then completely separated synthetic (±)-fragranol into each enantiomer by means of preparative high-performance liquid chromatography using a chiral resolution column, and (-)-(1S,2S)-fragranol was definitely confirmed to be the natural pheromone and to attract many males in the field when used as a pheromone trap lure. (±)-Fragranol showed attractiveness comparable to that of the pure (-)-(1S,2S)-enantiomer. This study provides not only useful information for the monitoring and management of P. marginatus but also an interesting exception underlining the great diversity of mealybug pheromone structures.

Indexed as

HemipteraSex AttractantsAnimalsCaricaChromatography, High Pressure LiquidFemaleGas Chromatography-Mass SpectrometryMagnetic Resonance SpectroscopyMaleMonoterpenesSexual Behavior, AnimalMonoterpenesSex AttractantsFragranolGrandisolMealybugMonoterpeneSex pheromone

Identifiers

PMID39904809
PMCPMC11794419

What OpenQuestion holds

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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.