Evidence map›Paper›PMID 41355278›Full record

ArticleAnnals of botany2026

Tri-trophic consequences of plant-to-plant volatile signalling and its contingency on plant relatedness in wild cotton.

Sandra Díaz-Cruz, Ted C J Turlings, Uriel Solís-Rodríguez, Jonathan Interian-Aguiñaga, Víctor Hugo Ramírez-Delgado, Mary V Clancy, Marine Mamin, Jonathan F Wendel, Corrinne E Grover, Mark A Arick and 6 more

Abstract read
In one paragraph

Article in Annals of botany, 2026. 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

16 authors.

Sandra Díaz-CruzDepartamento de Ecología Tropical, Campus de Ciencias Biológicas y Agropecuarias, Universidad Autónoma de Yucatán, Apartado Postal 4-116, Itzimná 97000, Mexico.
Ted C J TurlingsState Key Laboratory of Crop Stress Adaptation and Improvement, State Key Laboratory of Cotton Bio-Breeding and Integrated Utilization, School of Life Sciences, College of Agriculture, Henan University, Kaifeng 475004, China.
Uriel Solís-RodríguezUniversidad Nacional Autónoma de México, Escuela Nacional de Estudios Superiores Unidad Mérida, Carretera Mérida-Tetiz Km. 4.5, Ucú, Yucatán 97357, Mexico.
Jonathan Interian-AguiñagaDepartamento de Ecología Tropical, Campus de Ciencias Biológicas y Agropecuarias, Universidad Autónoma de Yucatán, Apartado Postal 4-116, Itzimná 97000, Mexico.
Víctor Hugo Ramírez-DelgadoDepartamento de Ecología Tropical, Campus de Ciencias Biológicas y Agropecuarias, Universidad Autónoma de Yucatán, Apartado Postal 4-116, Itzimná 97000, Mexico.
Mary V ClancyLaboratory of Fundamental and Applied Research in Chemical Ecology (FARCE), Institute of Biology, University of Neuchâtel, Rue Emile-Argand 11, Neuchâtel 2000, Switzerland.
Marine MaminLaboratory of Fundamental and Applied Research in Chemical Ecology (FARCE), Institute of Biology, University of Neuchâtel, Rue Emile-Argand 11, Neuchâtel 2000, Switzerland.
Jonathan F WendelDepartment of Ecology, Evolution, & Organismal Biology, Iowa State University, Ames, IA 50011, USA.
Corrinne E GroverDepartment of Ecology, Evolution, & Organismal Biology, Iowa State University, Ames, IA 50011, USA.
Mark A ArickInstitute for Genomics, Biocomputing & Biotechnology, Mississippi State University, Starkville, MS 39762, USA.
Chuan-Yu HsuInstitute for Genomics, Biocomputing & Biotechnology, Mississippi State University, Starkville, MS 39762, USA.
Olga PechanovaInstitute for Genomics, Biocomputing & Biotechnology, Mississippi State University, Starkville, MS 39762, USA.
Adam ThrashInstitute for Genomics, Biocomputing & Biotechnology, Mississippi State University, Starkville, MS 39762, USA.
Daniel G PetersonInstitute for Genomics, Biocomputing & Biotechnology, Mississippi State University, Starkville, MS 39762, USA.
Carlos Bustos-SeguraLaboratory of Fundamental and Applied Research in Chemical Ecology (FARCE), Institute of Biology, University of Neuchâtel, Rue Emile-Argand 11, Neuchâtel 2000, Switzerland.ORCID 0000-0002-8624-3251
Luis Abdala-RobertsUniversidad Nacional Autónoma de México, Escuela Nacional de Estudios Superiores Unidad Mérida, Carretera Mérida-Tetiz Km. 4.5, Ucú, Yucatán 97357, Mexico.ORCID 0000-0003-1394-3043

Funding

CONAHCYT master's scholarshipGenomics of MalvaceaeNational Natural Science Foundation of ChinaResearch Fund for International Scientists 3251102007Swiss National Science Foundation 315230_185319
6 · The paper itself

Abstract

BACKGROUND AND

aimsPlant volatile organic compounds (VOCs) induced by herbivory boost defences in neighbouring plants. These effects have been shown primarily for direct plant defences and are often stronger when emitter and receiver plants are genetically related. However, we know much less about how plant indirect defence is affected by VOC signalling. To address this, we conducted field experiments controlling for plant relatedness, testing the effects of VOC signalling on extrafloral nectar (EFN) production, a key indirect defence, and its impact on ant recruitment and attacks on herbivores of wild cotton (Gossypium hirsutum) plants.

methodsExperiments consisted of plant triplets, in which one individual acted as an emitter of VOCs and two as receivers. One receiver shared the same mother plant as the emitter, and the other was descended from a different mother. Half of the emitter plants were induced using the specialist caterpillar Alabama argillacea, and VOCs were collected. We then induced receivers and measured their EFN production, in addition to ant abundance and attack on sentinel caterpillars. We also subsequently excluded ants from half of the receivers to test for ant-mediated effects on natural herbivory occurring over the following weeks. KEY

resultsReceivers exposed to VOCs of damaged emitters produced a greater volume and concentration of EFN in response to herbivory relative to those exposed to undamaged emitters and, accordingly, showed higher rates of ant attack on sentinel caterpillars (albeit no differences in ant abundance). These effects were not contingent on emitter-receiver relatedness. In addition, we found no effect of ant exclusion on natural herbivory levels on receiver plants, although damage was low overall.

conclusionsThese findings provide insight into inter-plant VOC signalling effects on multitrophic interactions by revealing indirect defence induction that leads to herbivore reduction by ants but that such effect occurs independently of the degree of emitter-receiver relatedness.

Indexed as

GossypiumSignal TransductionVolatile Organic CompoundsAnimalsAntsHerbivoryLarvaMothsPlant NectarPlant NectarVolatile Organic CompoundsAnt–plant interactionextrafloral nectarGossypium hirsutum Lindirect defencespredationvolatile organic compounds

Identifiers

PMID41355278
PMCPMC13095879

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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.