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Floral heterochrony promotes flexibility of reproductive strategies in the morphologically homogeneous genus Eugenia (Myrtaceae)

https://doi.org/10.1093/aob/mcx142
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/j.1537-2197.1972.tb10113.xopenalex-snapshot
A RESOLUTION OF THE EUGENIA–SYZYGIUM CONTROVERSY (MYRTACEAE)
inferredcites →https://doi.org/10.1002/tax.591022openalex-snapshot
Floral formulae updated for routine inclusion in formal taxonomic descriptions
inferredcites →https://doi.org/10.1006/bojl.1993.1066openalex-snapshot
Dédoublement revisited: towards a renewed interpretation of the androecium of the Magnoliophytina
inferredcites →https://doi.org/10.1006/bojl.1993.1074openalex-snapshot
The distribution and systematic relevance of the androecial character polymery
inferredcites →https://doi.org/10.1007/bf00985910openalex-snapshot
Floral structure and evolution of primitive angiosperms: Recent advances
inferredcites →https://doi.org/10.1007/bf02857782openalex-snapshot
Heterochrony in plant evolutionary studies through the twentieth century
inferredcites →https://doi.org/10.1007/s00425-002-0942-yopenalex-snapshot
A comparison of early floral ontogeny in wild-type and floral homeotic mutant phenotypes of Primula
inferredcites →https://doi.org/10.1007/s00442-016-3564-yopenalex-snapshot
Floral asymmetry and predation risk modify pollinator behavior, but only predation risk decreases plant fitness
inferredcites →https://doi.org/10.1007/s00606-004-0161-zopenalex-snapshot
Floral development and systematic position of Arillastrum, Allosyncarpia, Stockwellia and Eucalyptopsis (Myrtaceae)
inferredcites →https://doi.org/10.1007/s12225-014-9493-1openalex-snapshot
Two new species of Brachystelma Sims (Apocynaceae: Asclepiadoideae-Ceropegieae) from the Western Ghats of India
inferredcites →https://doi.org/10.1007/s12225-014-9497-xopenalex-snapshot
A preliminary phylogenetic analysis of Eugenia (Myrtaceae: Myrteae), with a focus on Neotropical species
inferredcites →https://doi.org/10.1016/j.cub.2006.07.068openalex-snapshot
Evolution of Plant Breeding Systems
inferredcites →https://doi.org/10.1016/j.devcel.2009.05.005openalex-snapshot
Flower Morphogenesis: Timing Is Key
inferredcites →https://doi.org/10.1016/j.ppees.2016.11.001openalex-snapshot
Links between parallel evolution and systematic complexity in angiosperms—A case study of floral development in Myrcia s.l. (Myrtaceae)
inferredcites →https://doi.org/10.1016/j.ympev.2015.07.007openalex-snapshot
Interpreting the modern distribution of Myrtaceae using a dated molecular phylogeny
inferredcites →https://doi.org/10.1016/j.ympev.2015.10.001openalex-snapshot
Divergence times, historical biogeography, and shifts in speciation rates of Myrtales
inferredcites →https://doi.org/10.1016/j.ympev.2017.01.002openalex-snapshot
Myrteae phylogeny, calibration, biogeography and diversification patterns: Increased understanding in the most species rich tribe of Myrtaceae
inferredcites →https://doi.org/10.1016/s0024-4074(05)80002-6openalex-snapshot
The distribution and systematic relevance of the androecial character oligomery
inferredcites →https://doi.org/10.1016/s0065-2296(06)44001-5openalex-snapshot
Angiosperm Floral Evolution: Morphological Developmental Framework
inferredcites →https://doi.org/10.1017/cbo9781139013321.011openalex-snapshot
Floral ontogeny of Acacia celastrifolia: an enigmatic mimosoid legume with pronounced polyandry and multiple carpels
inferredcites →https://doi.org/10.1046/j.1420-9101.1989.2060409.xopenalex-snapshot
Heterochrony: Developmental mechanisms and evolutionary results
inferredcites →https://doi.org/10.1051/apido:19970104openalex-snapshot
Influence of floral visitation on nectar-sugar composition and nectary surface changes in Eucalyptus
inferredcites →https://doi.org/10.1071/bt14058openalex-snapshot
Development and evolution of the gynoecium in Myrteae (Myrtaceae)
inferredcites →https://doi.org/10.1071/bt9930511openalex-snapshot
Reproductive Biology of Australian Myrtaceae
inferredcites →https://doi.org/10.1071/sb09005openalex-snapshot
A taxonomic revision of Eucalyptus camaldulensis (Myrtaceae)
inferredcites →https://doi.org/10.1071/sb97041openalex-snapshot
Floral development in Melaleuca and Callistemon (Myrtaceae)
inferredcites →https://doi.org/10.1071/sb9910539openalex-snapshot
Floral development and systematic position of Eucalyptus curtisii (Myrtaceae)
inferredcites →https://doi.org/10.1080/0028825x.1986.10409725openalex-snapshot
The avoidance of interference between the presentation of pollen and stigmas in angiosperms I. Dichogamy
inferredcites →https://doi.org/10.1080/0028825x.1986.10409726openalex-snapshot
The avoidance of interference between the presentation of pollen and stigmas in angiosperms II. Herkogamy
inferredcites →https://doi.org/10.1080/0028825x.2002.9512824openalex-snapshot
Development of the hypanthium and androecium in New Zealand Myrtoideae (Myrtaceae)
inferredcites →https://doi.org/10.1080/0028825x.2003.9512836openalex-snapshot
Development of the hypanthium and androecium in South American Myrtoideae (Myrtaceae)
inferredcites →https://doi.org/10.1080/10549811.2017.1310049openalex-snapshot
GlobalTreeSearch: The first complete global database of tree species and country distributions
inferredcites →https://doi.org/10.1086/314211openalex-snapshot
Symmetry in Flowers: Diversity and Evolution
inferredcites →https://doi.org/10.1086/375319openalex-snapshot
Early Floral Development and Nature of the Calyptra in Eupomatiaceae (Magnoliales)
inferredcites →https://doi.org/10.1086/588071openalex-snapshot
The Branching Stamens ofRicinusand the Homologies of the Angiosperm Stamen Fascicle
inferredcites →https://doi.org/10.1093/aob/mch076openalex-snapshot
New Aspects in Floral Development of Papilionoideae: Initiated but Suppressed Bracteoles and Variable Initiation of Sepals
inferredcites →https://doi.org/10.1093/aob/mcn180openalex-snapshot
Comparative Anatomy and Morphology of Nectar-producing Melastomataceae
inferredcites →https://doi.org/10.1093/aob/mcq088openalex-snapshot
Evolution of exceptional species richness among lineages of fleshy-fruited Myrtaceae
inferredcites →https://doi.org/10.1093/aob/mcs124openalex-snapshot
Self-sterility in flowering plants: preventing self-fertilization increases family diversification rates
inferredcites →https://doi.org/10.1093/aob/mct189openalex-snapshot
Floral polymorphism and the fitness implications of attracting pollinating and florivorous insects
inferredcites →https://doi.org/10.1093/aob/mcv177openalex-snapshot
Space matters: meristem expansion triggers corona formation inPassiflora
inferredcites →https://doi.org/10.1098/rspb.2014.0075openalex-snapshot
Heterostyly accelerates diversification via reduced extinction in primroses
inferredcites →https://doi.org/10.1104/pp.102.017459openalex-snapshot
Floral Development in Legumes
inferredcites →https://doi.org/10.1111/boj.12328openalex-snapshot
Systematic and evolutionary implications of stamen position in Myrteae (Myrtaceae)
inferredcites →https://doi.org/10.1111/j.1095-8339.1991.tb00207.xopenalex-snapshot
The impact of receptacular growth on polyandry in the Myrtales
inferredcites →https://doi.org/10.1111/j.1438-8677.1998.tb00681.xopenalex-snapshot
Notes on the Evolution of Androecial Organisation in the Magnoliophytina (Angiosperms)
inferredcites →https://doi.org/10.1111/j.1469-8137.1994.tb03954.xopenalex-snapshot
Reproductive biology of eight sympatric Myrtaceae from Central Brazil
inferredcites →https://doi.org/10.1111/j.1469-8137.2004.01032.xopenalex-snapshot
Evolution of zygomorphy in monocot flowers: iterative patterns and developmental constraints
inferredcites →https://doi.org/10.1111/j.1558-5646.1977.tb00979.xopenalex-snapshot
POLLEN-OVULE RATIOS: A CONSERVATIVE INDICATOR OF BREEDING SYSTEMS IN FLOWERING PLANTS
inferredcites →https://doi.org/10.1111/j.1744-7429.2000.tb00619.xopenalex-snapshot
Patterns of Floristic Differentiation among Atlantic Forests in Southeastern Brazil and the Influence of Climate 1
inferredcites →https://doi.org/10.1111/j.1756-1051.1992.tb01839.xopenalex-snapshot
Complex polyandry in the Magnoliatae: definition, distribution and systematic value
inferredcites →https://doi.org/10.1146/annurev.es.16.110185.000311openalex-snapshot
Longevity of Individual Flowers
inferredcites →https://doi.org/10.1146/annurev.es.18.110187.002205openalex-snapshot
RELATIONSHIPS AMONG FLOWERS, FRUITS, AND SEEDS
inferredcites →https://doi.org/10.11646/phytotaxa.289.3.2openalex-snapshot
Sections in Eugenia (Myrteae, Myrtaceae): nomenclatural notes and a key
inferredcites →https://doi.org/10.15468/74y363openalex-snapshot
World Checklist of Selected Plant Families
inferredcites →https://doi.org/10.1590/0102-33062016abb0401openalex-snapshot
The flower anatomy of five species of Myrteae and its contribution to the taxonomy of Myrtaceae
inferredcites →https://doi.org/10.1590/s0102-33062007000100022openalex-snapshot
Biologia floral e da polinização de quatro espécies de Eugenia L. (Myrtaceae)
inferredcites →https://doi.org/10.1646/0006-3606(2000)032[0793:pofdaa]2.0.co;2openalex-snapshot
Patterns of Floristic Differentiation among Atlantic Forests in Southeastern Brazil and the Influence of Climate1
inferredcites →https://doi.org/10.1663/0006-8101(2002)068[0545:maasit]2.0.co;2openalex-snapshot
Morphology and Angiosperm Systematics in the Molecular Era
inferredcites →https://doi.org/10.2307/1940476openalex-snapshot
Pollen Removal From Tristylous Pontederia Cordata: Effects of Anther Position and Pollinator Specialization
inferredcites →https://doi.org/10.2307/2388002openalex-snapshot
Ecological Importance of Myrtaceae in an Eastern Brazilian Wet Forest
inferredcites →https://doi.org/10.2307/2399158openalex-snapshot
The Order Myrtales: Circumscription, Variation, and Relationships
inferredcites →https://doi.org/10.2307/2399990openalex-snapshot
A Survey of the Reproductive Biology of the Myrtoideae (Myrtaceae)
inferredcites →https://doi.org/10.2307/2419835openalex-snapshot
Diversity and Evolutionary Biology of Tropical Flowers.
inferredcites →https://doi.org/10.26512/2014.10.t.18256openalex-snapshot
Revisão taxonômica e filogenia de Eugenia sect. Pilothecium (Kiaersk.) D. Legrand (Myrtaceae)
inferredcites →https://doi.org/10.3732/ajb.1300355openalex-snapshot
Comparative development of rare cases of a polycarpellate gynoecium in an otherwise monocarpellate family, Leguminosae
inferredcites →https://doi.org/10.3732/ajb.1400509openalex-snapshot
Floral cost vs. floral display: Insights from the megadiverse Myrtales suggest that energetically expensive floral parts are less phylogenetically constrained
inferredcites →https://doi.org/10.3897/phytokeys.61.7904openalex-snapshot
Circumscription and synopsis of Eugenia section Speciosae Bünger & Mazine (Myrtaceae)
inferredcites →https://doi.org/10.5281/zenodo.15955417openalex-snapshot
Evolution in the Myrtaceae - Evidence from inflorescence structure
inferredcites →https://doi.org/10.5860/choice.48-3861openalex-snapshot
Floral diagrams: an aid to understanding flower morphology and evolution
inferredcites →https://doi.org/10.5860/choice.49-2063openalex-snapshot
Pollination and floral ecology

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.11646/phytotaxa.362.3.4zenodo-depositor-declared
Nomenclatural notes on Eugenia with closed calyces: Calycorectes O.Berg and Mitranthes O.Berg (Myrtaceae)
inferred← citeshttps://doi.org/10.11646/phytotaxa.508.2.4zenodo-depositor-declared
Systematics studies in Pliniinae (Myrtaceae) necessitate two new combinations in Eugenia (Myrtaceae)
inferred← citeshttps://doi.org/10.11646/phytotaxa.524.3.1zenodo-depositor-declared
Taxonomic monograph of Eugenia sect. Schizocalomyrtus (Myrtaceae: Myrteae), a group within Eugenia with unusual flowers
inferred← citeshttps://doi.org/10.11646/phytotaxa.543.1.3zenodo-depositor-declared
A tribute to resistance: Eugenia quilombola (Myrtaceae), a new species with multilocular anthers from the Atlantic Forest of northeastern Brazil
inferred← citeshttps://doi.org/10.11646/phytotaxa.642.1.2zenodo-depositor-declared
Polysporangiate anthers described in Eugenia (Myrtaceae) with notes on evolutionary patterns
inferred← citeshttps://doi.org/10.5091/plecevo.152818zenodo-depositor-declared
And the twain shall meet at the end: a phylogeny of Myrcianthes (Myrtaceae, Myrteae) with phytogeographic and morphological insights
inferred← citeshttps://doi.org/10.1002/ajb2.16330openalex-snapshot
Towards a species‐level phylogeny for Neotropical Myrtaceae: Notes on topology and resources for future studies
inferred← citeshttps://doi.org/10.1002/ajb2.1655openalex-snapshot
Evolutionary lability in floral ontogeny affects pollination biology in Trimezieae
inferred← citeshttps://doi.org/10.1002/ece3.70670openalex-snapshot
Petrocodon gracilis (Gesneriaceae), a New Species From Southwestern Guangxi, China
inferred← citeshttps://doi.org/10.1002/tax.12263openalex-snapshot
A phylogenetic survey of Myrtaceae in the Greater Antilles with nomenclatural changes for some endemic species
inferred← citeshttps://doi.org/10.1007/s00425-025-04825-8openalex-snapshot
Morphoanatomy, patterns of development and types of feijoa (Acca sellowiana) flower buds in tropical and subtropical climates
inferred← citeshttps://doi.org/10.1007/s10265-018-1057-2openalex-snapshot
Staminate flower of Prunus s. l. (Rosaceae) from Eocene Rovno amber (Ukraine)
inferred← citeshttps://doi.org/10.1007/s12225-025-10264-1openalex-snapshot
Eugenia venteri (sect. Jossinia, Myrtaceae): a new flagelliflorous tree from the rainforest of Manus Island, Papua New Guinea
inferred← citeshttps://doi.org/10.1007/s12225-025-10343-3openalex-snapshot
Eugenia magnicarpa, a new species with one of the largest fruits of Eugenia, from the Brazilian Atlantic Forest
inferred← citeshttps://doi.org/10.1016/j.cbi.2021.109429openalex-snapshot
Eugenia piauhiensis Vellaff. essential oil and γ-elemene its major constituent exhibit antileishmanial activity, promoting cell membrane damage and in vitro immunomodulation
inferred← citeshttps://doi.org/10.1016/j.ecoinf.2024.102490openalex-snapshot
The Atlantic forest is a potentially climatic suitable habitat for four Neotropical Myrtaceae species through time
inferred← citeshttps://doi.org/10.1016/j.flora.2021.151969openalex-snapshot
The ontogeny of the pericarp in the subtribe Eugeniinae O. Berg (Myrteae, Myrtaceae) reveals a drupe-like fruit in Myrcianthes pungens (O. Berg) D. Legrand
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112802openalex-snapshot
Heterochrony may underpin the domestication of soybean seed and pod morphology
inferred← citeshttps://doi.org/10.1016/j.ppees.2021.125591openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ppees.2025.125887openalex-snapshot
Ontogeny unlocks the floral development and evolution of Uleanthus, a florally divergent monospecific genus of Amazonian legume trees
inferred← citeshttps://doi.org/10.1016/j.tig.2024.06.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tplants.2023.07.013openalex-snapshot
Flower heterochrony and crop yield
inferred← citeshttps://doi.org/10.1016/j.ympev.2019.106553openalex-snapshot
Calyx (con)fusion in a hyper-diverse genus: Parallel evolution of unusual flower patterns in Eugenia (Myrtaceae)
inferred← citeshttps://doi.org/10.1080/23818107.2026.2660203openalex-snapshot
Typification of and nomenclatural notes on Eugenia L. (Myrtaceae) from the Amazon
inferred← citeshttps://doi.org/10.1093/aob/mcab100openalex-snapshot
Floral development and vasculature in Eriocaulon (Eriocaulaceae) provide insights into the evolution of Poales
inferred← citeshttps://doi.org/10.1093/aob/mcad080openalex-snapshot
Weak latitudinal trends in reproductive traits of Afromontane forest trees
inferred← citeshttps://doi.org/10.1093/aob/mcaf275openalex-snapshot
Developmental timing in the female reproductive cycle of Araucaria araucana : seasonality and evolutionary perspectives
inferred← citeshttps://doi.org/10.1093/botlinnean/boab050openalex-snapshot
Spicoid morphology of Mapanioideae (Cyperaceae): an evolutionary perspective
inferred← citeshttps://doi.org/10.1093/botlinnean/boab095openalex-snapshot
Advances and perspectives on the evolutionary history and diversification of Neotropical Myrteae (Myrtaceae)
inferred← citeshttps://doi.org/10.1093/botlinnean/boaf017openalex-snapshot
When disparity arises: heterochronic development of spiral ginger flowers with contrasting pollination syndromes
inferred← citeshttps://doi.org/10.1093/botlinnean/boaf041openalex-snapshot
Revisiting floral ontogeny of the papilionoid legume Dipterygeae clade: insights from the florally divergent Amazonian genus Monopteryx
inferred← citeshttps://doi.org/10.1093/botlinnean/boag029openalex-snapshot
Floral ontogeny of Cleobulia (Leguminosae: Papilionoideae), the dwarf winged genus within the Dioclea clade
inferred← citeshttps://doi.org/10.1093/botlinnean/boz029openalex-snapshot
Comparative floral structure and evolution in Galipeinae (Galipeeae: Rutaceae) and its implications at different systematic levels
inferred← citeshttps://doi.org/10.1111/nph.15453openalex-snapshot
Floral uniformity through evolutionary time in a species‐rich tree lineage
inferred← citeshttps://doi.org/10.11606/t.41.2021.tde-09122021-141322openalex-snapshot
Diversidade e evolução do sistema vascular em Nyctaginaceae (Caryophyllales)
inferred← citeshttps://doi.org/10.12705/674.5openalex-snapshot
Phylogeny and biogeography of the hyper–diverse genus Eugenia (Myrtaceae: Myrteae), with emphasis on E . sect. Umbellatae , the most unmanageable clade
inferred← citeshttps://doi.org/10.1590/1677-941x-abb-2022-0194openalex-snapshot
Myrtaceae Juss. in restinga of Bahia: diversity, taxonomy, and distribution
inferred← citeshttps://doi.org/10.1590/2175-7860202475076openalex-snapshot
Floral anatomy of 12 species of the subtribe Myrciinae (Myrteae, Myrtaceae)
inferred← citeshttps://doi.org/10.1600/036364419x15620113920608openalex-snapshot
A New Subtribal Classification of Tribe Myrteae (Myrtaceae)
inferred← citeshttps://doi.org/10.1600/036364419x15620113920617openalex-snapshot
A Systematic Overview of the Floral Diversity in Myrteae (Myrtaceae)
inferred← citeshttps://doi.org/10.1600/036364419x697903openalex-snapshot
Phylogenetic Placement of New Species with Fused Calyx Reveals Homoplastic Character in Eugenia (Myrtaceae)
inferred← citeshttps://doi.org/10.1600/036364422x16573019348319openalex-snapshot
A Taxonomic Revision of the Lathberry Clade of Eugenia (Myrtaceae)
inferred← citeshttps://doi.org/10.2139/ssrn.4837261openalex-snapshot
And the Twain Shall Meet at the End: A Phylogeny of Myrcianthes (Myrtaceae, Myrteae) with Phytogeographical, Taxonomical and Morphological Insights
inferred← citeshttps://doi.org/10.25148/etd.fidc009191openalex-snapshot
Systematic Studies in Myrtaceae of the Greater and Lesser Antilles
inferred← citeshttps://doi.org/10.3389/fpls.2018.01349openalex-snapshot
The Times They Are A-Changin’: Heterochrony in Plant Development and Evolution
inferred← citeshttps://doi.org/10.3389/fpls.2021.759460openalex-snapshot
Phylogenetic Relationships Within the Hyper-Diverse Genus Eugenia (Myrtaceae: Myrteae) Based on Target Enrichment Sequencing
inferred← citeshttps://doi.org/10.3390/plants15040646openalex-snapshot
Unveiling the Biotechnological and Agronomic Potential of Amazonian Fruit Species from the Genus Eugenia (Myrtaceae): Functional Traits and Applied Perspectives
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