Evidence map›Paper›PMID 42762363›Full record

ArticlePlanta2026

Floral dynamics in the protandrous flowers of Bauhinia variegata (Fabaceae): phase-specific morphology, scent, and nectar production.

Andrews Vinicius Santos da Silva, Vidal de Freitas Mansano, Dalton Guimarães Veloso, Ana Claudia Fernandes Amaral, Jefferson Diocesano da Cruz, Fabrício de Oliveira Silva, Walter Sotto Mayor Fernandes Neto, Jefferson Rocha de Andrade Silva, Pedro Joaquim Bergamo, Leandro Freitas and 1 more

Abstract read
In one paragraph

Article in Planta, 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

11 authors.

Andrews Vinicius Santos da SilvaPrograma de Pós-Graduação em Botânica, Escola Nacional de Botânica Tropical, Instituto de Pesquisas Jardim Botânico do Rio de Janeiro, Rua Pacheco Leão 2040, Rio de Janeiro, RJ, 22460-036, Brazil.
Vidal de Freitas MansanoPrograma de Pós-Graduação em Botânica, Escola Nacional de Botânica Tropical, Instituto de Pesquisas Jardim Botânico do Rio de Janeiro, Rua Pacheco Leão 2040, Rio de Janeiro, RJ, 22460-036, Brazil.
Dalton Guimarães VelosoFaculdade de Farmácia, Programa de Pós-Graduação em Ciências Farmacêuticas, Centro de Ciências da Saúde, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, RJ, 21949-900, Brazil.
Ana Claudia Fernandes AmaralLaboratório de Plantas Medicinais e Derivados, Farmanguinhos, Fundação Oswaldo Cruz, Rio de Janeiro, RJ, 21041-250, Brazil.
Jefferson Diocesano da CruzLaboratório de Plantas Medicinais e Derivados, Farmanguinhos, Fundação Oswaldo Cruz, Rio de Janeiro, RJ, 21041-250, Brazil.
Fabrício de Oliveira SilvaDepartamento de Produtos Naturais e Alimentos, Faculdade de Farmácia, Centro de Ciências da Saúde, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, RJ, 21941-902, Brazil.
Walter Sotto Mayor Fernandes NetoDepartamento de Química, Laboratório de Cromatografia, Instituto de Ciências Exatas, Universidade Federal do Amazonas (UFAM), Manaus, AM, 69077-000, Brazil.
Jefferson Rocha de Andrade SilvaDepartamento de Química, Laboratório de Cromatografia, Instituto de Ciências Exatas, Universidade Federal do Amazonas (UFAM), Manaus, AM, 69077-000, Brazil. jrocha_01@yahoo.com.br.ORCID http://orcid.org/0000-0003-2569-1306
Pedro Joaquim BergamoInstituto de Biociências, Universidade Estadual Paulista (UNESP), Câmpus de Rio Claro, Avenida 24 A, Rio Claro, SP, 151513506-900, Brazil.
Leandro FreitasInstituto de Pesquisas Jardim Botânico do Rio de Janeiro, DIPEQ, Rua Pacheco Leão 915, Rio de Janeiro, RJ, 22460-030, Brazil.
Juliana Villela PaulinoPrograma de Pós-Graduação em Botânica, Escola Nacional de Botânica Tropical, Instituto de Pesquisas Jardim Botânico do Rio de Janeiro, Rua Pacheco Leão 2040, Rio de Janeiro, RJ, 22460-036, Brazil. jvillelapaulino@farmacia.ufrj.br.ORCID http://orcid.org/0000-0003-0072-639X

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 315237/2023-6Conselho Nacional de Desenvolvimento Científico e Tecnológico 406238/2022-7Conselho Nacional de Desenvolvimento Científico e Tecnológico 447621/2024-6Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 88887.721965/2022-00Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/204.527/2025 -BBPFundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/210.827/2025Fundação de Amparo à Pesquisa do Estado do Amazonas 01.02.016301.02461/2025-17
6 · The paper itself

Abstract

MAIN

conclusionProtandry in Bauhinia variegata is expressed through coordinated changes in floral morphology, scent composition, secretory activity, and nectar presentation, whereas petal reflectance remains stable; molecular docking further indicates that key phase-associated volatiles are structurally compatible with a bee odourant-binding protein, supporting mechanistic plausibility of olfactory detectability without demonstrating behavioral attraction. Bauhinia variegata exhibits protandrous flowers in which floral morphology, scent production, and nectar presentation change through anthesis. Here, we examined anthesis, stigma receptivity, petal reflectance, volatile organic compound (VOC) composition across floral organs and phases, secretory structures, nectar dynamics, and the structural compatibility of selected phase-discriminant VOCs with a honeybee odourant-binding protein. Flowers exhibited prolonged anthesis, opening at night and remaining functional for 2-3 days. Pollen release predominated during the 1st day (staminate phase), whereas maximal stigma receptivity occurred on the 2nd day (pistillate phase), accompanied by elongation and curvature of the style. Petal reflectance remained stable across phases. Floral scent was spatially heterogeneous among organs and temporally dynamic across anthesis, with terpene-rich bouquets dominated by α-pinene and β-pinene and with phase- or organ-informative compounds including nonanal, limonene, trans-caryophyllene, and 6-methyl-5-hepten-2-one. Cavitated secretory trichomes and sepals showed evidence of terpene-associated secretion. Nectar volume and total sugar content peaked during the pistillate phase, coinciding with strongest stigma receptivity. Molecular docking with AmelOBP14 showed that key phase-associated VOCs are structurally compatible with a bee odourant-binding protein, providing complementary mechanistic support for their potential olfactory detectability. Together, these results show that protandry in B. variegata is expressed through coordinated changes in morphology, scent, secretory activity, and nectar presentation, indicating a complex signalling strategy; however behavioural responses of floral visitors remain to be tested.

Indexed as

BauhiniaFlowersOdorantsPlant NectarAnimalsBeesMolecular Docking SimulationPollinationVolatile Organic CompoundsPlant NectarVolatile Organic CompoundsDichogamyFloral scentMolecular dockingNectar dynamicsProtandryVolatile organic compounds

Identifiers

PMID42762363
PMCPMC13589757

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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.