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Flowering Phenology and Diversity in Tropical Bignoniaceae

https://doi.org/10.2307/2989698
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What this work says

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

inferredcites →https://doi.org/10.1007/978-3-642-51863-8_24openalex-snapshot
Tropical Plant Phenology: Applications for Studies in Community Ecology
inferredcites →https://doi.org/10.1111/j.1558-5646.1967.tb03416.xopenalex-snapshot
SYNCHRONIZATION OF SEXUAL REPRODUCTION OF TREES WITHIN THE DRY SEASON IN CENTRAL AMERICA
inferredcites →https://doi.org/10.1126/science.132.3423.354openalex-snapshot
Moisture Stress as a Requirement for Flowering of Coffee
inferredcites →https://doi.org/10.1126/science.171.3967.203openalex-snapshot
Euglossine Bees as Long-Distance Pollinators of Tropical Plants
inferredcites →https://doi.org/10.1146/annurev.pp.22.060171.002053openalex-snapshot
Flower Induction and the Florigen Concept
inferredcites →https://doi.org/10.2307/3543864openalex-snapshot
Competition for Pollinators as a Stimulus for the Evolution of Flowering Time

What points at this work

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

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Staminode of Jacaranda rugosa A.H. Gentry (Bignoniaceae) promotes functional specialization by ensuring signaling and mechanical fit to medium-sized bees
inferred← citeshttps://doi.org/10.11646/phytotaxa.278.1.2zenodo-depositor-declared
An inventory of the Bignoniaceae from the Brazilian state of Rio Grande do Norte highlights the importance of small herbaria to biodiversity studies
inferred← citeshttps://doi.org/10.11646/phytotaxa.570.2.4zenodo-depositor-declared
Floristic Inventory of the Iguaçu and Iguazú National Parks (Brazil and Argentina): Bignoniaceae
inferred← citeshttps://doi.org/10.11646/phytotaxa.616.2.11zenodo-depositor-declared
A new combination in Dolichandra (Bignoniaceae) from Brazil
inferred← citeshttps://doi.org/10.1002/9780470292082.biblioopenalex-snapshot
Literature Cited
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Reproductive consequences of variation in flowering phenology in the dry forest tree Enterolobium cyclocarpum in Guanacaste, Costa Rica
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Quantitative comparison of flowering phenology traits among trees, perennial herbs, and annuals in a temperate plant community
inferred← citeshttps://doi.org/10.1002/ajb2.1399openalex-snapshot
Phylogeny of the Neotropical tribe Jacarandeae (Bignoniaceae)
inferred← citeshttps://doi.org/10.1002/ajb2.1533openalex-snapshot
Facilitation with a grain of salt: reduced pollinator visitation is an indirect cost of association with the foundation species creosote bush (Larrea tridentata)
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Plant species with the trait of continuous flowering do not hold core roles in a Neotropical lowland plant‐pollinating insect network
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Different Flowering Strategies Ensure Reproductive Success in Two Coexisting Self‐Incompatible Orchids
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Good to the Last Drop? Nectar Depletion by Insect Pollinators Varies Among Plant Species and Through Time
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Multiscale phenological niches of seed fall in diverse A mazonian plant communities
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THE POLLINATION BIOLOGY OF TILIA
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FLORAL BIOLOGY, HUMMINGBIRD POLLINATION AND FRUIT PRODUCTION OF TRUMPET CREEPER (CAMPSIS RADICANS, BIGNONIACEAE)
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Floral resource diversity drives spatiotemporal variation in plant–pollinator network structure
inferred← citeshttps://doi.org/10.1002/tax.13028openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/tax.593015openalex-snapshot
The reproductive biology of Voyria (Gentianaceae) species in French Guiana
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inferred← citeshttps://doi.org/10.1006/jare.2001.0801openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-0-387-30599-8_5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-4613-1165-2_11openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-4613-3421-7_8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-4613-3421-7_9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-4614-7397-8_11openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-4615-6956-5_4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-17854-3_60-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-35940-9_3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-44963-6_10openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-44963-6_12openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-57635-6_60openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-031-05942-1_10openalex-snapshot
Bignoniaceae to Buxaceae
inferred← citeshttps://doi.org/10.1007/978-3-031-75027-4_8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-14397-7_7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-68153-0_16openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-90-481-8725-6_5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-94-007-0632-3_9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-94-007-6925-0_9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-94-009-5500-4_24openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-94-011-0717-4_11openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-10-7260-4_3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-15-4210-7_1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00317246openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00344650openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00377521openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00378992openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00379114openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00936071openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00936097openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00937708openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00983208openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00984909openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00985349openalex-snapshot
Some pollination strategies in neotropical savannas and forests
inferred← citeshttps://doi.org/10.1007/bf00988909openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf01237757openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf02361207openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf02860857openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf03030550openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/pl00012018openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00040-016-0466-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00114-021-01756-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00114-023-01873-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00114-024-01912-wopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00114-024-01924-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00114-025-02028-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00442-024-05616-wopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00468-004-0405-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00468-020-02056-wopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00606-007-0628-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00606-011-0430-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00606-011-0432-4openalex-snapshot
Pollen partitioning of three species of Convolvulaceae among oligolectic bees in the Caatinga of Brazil
inferred← citeshttps://doi.org/10.1007/s00606-012-0706-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00606-014-1191-9openalex-snapshot
Phenotypic differences are not explained by pre-zygotic reproductive barriers in sympatric varieties of the Humiria balsamifera complex (Humiriaceae)
inferred← citeshttps://doi.org/10.1007/s00606-016-1291-9openalex-snapshot
Sporophytic apomixis in polyembryonic Handroanthus serratifolius (Vahl) S.O. Grose (Bignoniaceae) characterizes the species as an agamic polyploid complex
inferred← citeshttps://doi.org/10.1007/s006060200031openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10336-019-01712-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10457-020-00533-2openalex-snapshot
Growth, flowering and fruiting of Campomanesia adamantium (Cambess) O. Berg intercropped with green manure species in Agroforestry Systems
inferred← citeshttps://doi.org/10.1007/s10531-010-9975-xopenalex-snapshot
Synchronous phenology of hawkmoths (Sphingidae) and Inga species (Fabaceae–Mimosoideae): implications for the restoration of the Atlantic forest of northeastern Brazil
inferred← citeshttps://doi.org/10.1007/s10592-011-0292-zopenalex-snapshot
Mating system parameters at hierarchical levels of fruits, individuals and populations in the Brazilian insect-pollinated tropical tree, Tabebuia roseo-alba (Bignoniaceae)
inferred← citeshttps://doi.org/10.1007/s10666-006-9063-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10682-006-9109-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10682-007-9190-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10722-026-02738-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11258-018-0792-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11258-025-01579-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11284-010-0799-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11284-013-1050-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11284-018-1625-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11295-018-1230-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11629-010-1107-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11756-025-01931-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12224-022-09412-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12228-014-9337-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13364-016-0306-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13592-015-0354-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13592-016-0456-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s40415-018-00512-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s40415-021-00765-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s44473-026-00178-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0305-1978(80)90058-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0305-1978(94)90099-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-353550-4.50017-4openalex-snapshot
Speciation in tropical forests
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inferred← citeshttps://doi.org/10.1016/b978-0-12-583980-8.50018-1openalex-snapshot
Microbehavior and Macrostructure in Pollinator–Plant Interactions
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On Uncertainty and the Law of Diminishing Returns in Evolution and Behavior
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DIPTEROCARP REPRODUCTIVE BIOLOGY
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Evidence of genetic influence on the flowering pattern of Ficus microcarpa
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inferred← citeshttps://doi.org/10.1016/j.anbehav.2011.12.025openalex-snapshot
Repeated unrewarded scent exposure influences the food choice of stingless bee foragers, Melipona scutellaris
inferred← citeshttps://doi.org/10.1016/j.biocon.2010.03.036openalex-snapshot
Agricultural surroundings support flower–visitor networks in an Afrotropical rain forest
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Eavesdropping selects for conspicuous signals
inferred← citeshttps://doi.org/10.1016/j.dib.2018.02.037openalex-snapshot
Dataset on leaf surface and elemental study of four species of Bignoniaceae family by SEM-EDAX
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The dioecious, sphingophilous species Citharexylum myrianthum (Verbenaceae): Pollination and visitor diversity
inferred← citeshttps://doi.org/10.1016/j.flora.2007.04.001openalex-snapshot
Fruiting phenology in a tropical dry evergreen forest on the Coromandel coast of India in relation to plant life-forms, physiognomic groups, dispersal modes, and climatic constraints
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Phenology, pollination, and breeding system of the threatened tree Caesalpinia echinata Lam. (Fabaceae), and a review of studies on the reproductive biology in the genus
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inferred← citeshttps://doi.org/10.1016/j.flora.2010.12.004openalex-snapshot
The importance of bees as pollinators in the short corolla bromeliad Aechmea caudata in southern Brazil
inferred← citeshttps://doi.org/10.1016/j.flora.2011.01.004openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.flora.2011.05.004openalex-snapshot
The reproductive biology of Cybistax antisyphilitica (Bignoniaceae), a characteristic tree of the South American savannah-like “Cerrado” vegetation
inferred← citeshttps://doi.org/10.1016/j.flora.2013.04.008openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.flora.2013.05.003openalex-snapshot
Two sympatric Byrsonima species (Malpighiaceae) differ in phenological and reproductive patterns
inferred← citeshttps://doi.org/10.1016/j.flora.2014.04.004openalex-snapshot
Conditional outcomes in ant–plant–herbivore interactions influenced by sequential flowering
inferred← citeshttps://doi.org/10.1016/j.flora.2016.04.009openalex-snapshot
Pollination biology and breeding system of syntopic Adenocalymma nodosum and A. peregrinum (Bignonieae, Bignoniaceae) in the Brazilian savanna
inferred← citeshttps://doi.org/10.1016/j.flora.2017.02.024openalex-snapshot
Flowering phenology and plant-pollinator interactions in a grassland community of Southern Brazil
inferred← citeshttps://doi.org/10.1016/j.flora.2020.151660openalex-snapshot
One or two species? Floral characteristics and pollination biology aid in Sinningia (Gesneriaceae) species circumscription
inferred← citeshttps://doi.org/10.1016/j.flora.2021.151966openalex-snapshot
Centres of endemism in Borneo and their environmental correlates revealed by endemic plant genera
inferred← citeshttps://doi.org/10.1016/j.foreco.2019.117593openalex-snapshot
Phenology, flowering and fruit-set patterns of baobabs, Adansonia digitata, in southern Africa
inferred← citeshttps://doi.org/10.1016/j.jaridenv.2015.09.015openalex-snapshot
Vertebrate mixed pollination system in Encholirium spectabile: A bromeliad pollinated by bats, opossum and hummingbirds in a tropical dry forest
inferred← citeshttps://doi.org/10.1016/j.mambio.2011.08.001openalex-snapshot
Transient yellow colouration of the bat Artibeus jamaicensis coincides with pollen consumption
inferred← citeshttps://doi.org/10.1016/j.ufug.2014.08.002openalex-snapshot
Spatiotemporal distribution of floral resources in a Brazilian city: Implications for the maintenance of pollinators, especially bees
inferred← citeshttps://doi.org/10.1016/j.ufug.2021.127238openalex-snapshot
Phenological advance of blossoming over the past century in one of the world’s largest urban forests, Gauteng City-Region, South Africa
inferred← citeshttps://doi.org/10.1016/j.ufug.2021.127412openalex-snapshot
A nectar oasis for urban Glossophaginae bats: Temporal resource dynamics of the chiropterophilous Crescentia cujete (Bignoniaceae)
inferred← citeshttps://doi.org/10.1016/j.ympev.2014.12.008openalex-snapshot
Speciation within Columnea section Angustiflora (Gesneriaceae): Islands, pollinators and climate
inferred← citeshttps://doi.org/10.1016/s0367-2530(17)30674-6openalex-snapshot
Hawkmoth pollination in Cereus peruvianus, a columnar cactus from southeastern Brazil
inferred← citeshttps://doi.org/10.1016/s0367-2530(17)30718-1openalex-snapshot
Dioecy in the Cerrado vegetation of Central Brazil
inferred← citeshttps://doi.org/10.1016/s0367-2530(17)30990-8openalex-snapshot
Reproductive biology of woody plants in a cerrado community of Central Brazil
inferred← citeshttps://doi.org/10.1017/cbo9780511541971.014openalex-snapshot
Impacts of herbivores on tropical plant diversity
inferred← citeshttps://doi.org/10.1017/s0266467400002984openalex-snapshot
Phenological studies of shrub and treelet species in tropical cloud forests of Costa Rica
inferred← citeshttps://doi.org/10.1017/s0266467400004260openalex-snapshot
Phenology, seed dispersal, and recruitment in Cecropia peltata (Moraceae) in Costa Rican tropical dry forest
inferred← citeshttps://doi.org/10.1017/s026646740001052xopenalex-snapshot
Spatial distribution, fruit production and seed removal of a rare, dioecious canopy tree species (Aglaia aff. flavida Merr. et Perr.) in Papua New Guinea
inferred← citeshttps://doi.org/10.1017/s026646740800521xopenalex-snapshot
The pollination ecology of the late-successional tree, Oroxylum indicum (Bignoniaceae) in Thailand
inferred← citeshttps://doi.org/10.1017/s0266467413000217openalex-snapshot
Is the São Francisco River a geographic barrier to gene flow in trees ofHandroanthus ochraceus?
inferred← citeshttps://doi.org/10.1017/s0266467499000693openalex-snapshot
Reproductive phenology and mating potential in a low density tree population of Couratari multiflora (Lecythidaceae) in central Amazonia
inferred← citeshttps://doi.org/10.1017/s0266467499000954openalex-snapshot
Reproductive phenology of sympatric taxa of Chamaecrista (Leguminosae) in Serra do Cipó, Brazil
inferred← citeshttps://doi.org/10.1017/s0266467499001091openalex-snapshot
Temporal patterns of individual and group foraging behaviour in the short-nosed fruit bat, Cynopterus sphinx, in south India
inferred← citeshttps://doi.org/10.1017/s1479262123000655openalex-snapshot
Prospection of ISSR primers and population genetic characterization of Paratecoma peroba (Record) Kuhlm.
inferred← citeshttps://doi.org/10.1023/a:1020356706052openalex-snapshot
Flowering phenology and female reproductive success in Silene acutifolia Link ex Rohrb
inferred← citeshttps://doi.org/10.1038/hdy.2010.134openalex-snapshot
Temporal variation in pollen dispersal and breeding structure in a bee-pollinated Neotropical tree
inferred← citeshttps://doi.org/10.1055/s-2003-40802openalex-snapshot
The Hummingbird Plant Community of a Tropical Montane Rain Forest in Southern Ecuador
inferred← citeshttps://doi.org/10.1055/s-2004-820979openalex-snapshot
Non‐Euglossine Bees also Function as Pollinators of Sinningia Species (Gesneriaceae) in Southeastern Brazil
inferred← citeshttps://doi.org/10.1055/s-2005-865619openalex-snapshot
The Pollination of Bromelia antiacantha (Bromeliaceae) in Southeastern Brazil: Ornithophilous versus Melittophilous Features
inferred← citeshttps://doi.org/10.1071/bt9950103openalex-snapshot
Variation in Flowering Parameters Within and Among Five Species of Australian Alpine Ranunculus
inferred← citeshttps://doi.org/10.1080/00218839.1990.11101201openalex-snapshot
The Flowering Periods of Leguminosae in the Yucatan Peninsula in Relation to Honey Flows
inferred← citeshttps://doi.org/10.1080/00222930500392659openalex-snapshot
Reproductive phenology and pre‐dispersal seed‐feeding inProtium tovarense(Burseraceae), with a description of the first known phytophagous “Bracon” species (Hymenoptera: Braconidae: Braconinae)
inferred← citeshttps://doi.org/10.1080/00222930802478651openalex-snapshot
Vegetation complexity and bat‐plant dispersal in Calakmul, Mexico
inferred← citeshttps://doi.org/10.1080/00222933.2011.552797openalex-snapshot
Reproductive phenology and flower visitors' guild ofCanistropsis microps(Bromeliaceae) in an Atlantic Rainforest of southeastern Brazil
inferred← citeshttps://doi.org/10.1080/0028825x.1985.10434229openalex-snapshot
Flowering and fruiting patterns of three species of Melicytus (Violaceae) in New Zealand
inferred← citeshttps://doi.org/10.1080/01650521.2017.1396804openalex-snapshot
Fruit digestion time, integrity and germination of seeds defecated byArtibeus lituratus(Olfers, 1818) (Chiroptera: Phyllostomidae)
inferred← citeshttps://doi.org/10.1080/12538078.2008.10516108openalex-snapshot
Flowering and fruiting phenology in maquis of New Caledonia
inferred← citeshttps://doi.org/10.1080/12538078.2012.671654openalex-snapshot
Diversité spatiotemporelle des ressources florales autour d’un rucher en zone de végétation de transition soudano-guinéenne au Bénin
inferred← citeshttps://doi.org/10.1080/17429145.2016.1179803openalex-snapshot
Determining suitable grazing time for Puccinella distans Parl. based on its phenology in West Azerbaijan Province of Iran
inferred← citeshttps://doi.org/10.1080/17550874.2019.1566409openalex-snapshot
Bat pollination in Bromeliaceae
inferred← citeshttps://doi.org/10.1080/23818107.2025.2450826openalex-snapshot
Reproductive phenology and pollination biology of the wild pineapple Ananas bracteatus (Bromeliaceae): an analysis based on field and herbarium records
inferred← citeshttps://doi.org/10.1086/314187openalex-snapshot
Flower Structure and Reproductive Biology in Aspidosperma quebracho‐blanco (Apocynaceae), a Tree Pollinated by Deceit
inferred← citeshttps://doi.org/10.1088/1748-9326/11/11/115003openalex-snapshot
Synchrony, compensatory dynamics, and the functional trait basis of phenological diversity in a tropical dry forest tree community: effects of rainfall seasonality
inferred← citeshttps://doi.org/10.1093/aob/mcad193openalex-snapshot
Better soon than never: climate change induces strong phenological reassembly in the flowering of a Mediterranean shrub community
inferred← citeshttps://doi.org/10.1093/aob/mcag096openalex-snapshot
Impostors in South America: a new Batesian floral mimicry system involving orchids and Bignoniaceae models
inferred← citeshttps://doi.org/10.1093/aob/mcf169openalex-snapshot
Secretory Trichomes, a Substitutive Floral Nectar Source in Lundia A. DC. (Bignoniaceae), a Genus Lacking a Functional Disc
inferred← citeshttps://doi.org/10.1093/aob/mcf204openalex-snapshot
A Stochastic Flowering Model Describing an Asynchronically Flowering Set of Trees
inferred← citeshttps://doi.org/10.1093/aob/mcg192openalex-snapshot
Aechmea pectinata: a Hummingbird-dependent Bromeliad with Inconspicuous Flowers from the Rainforest in South-eastern Brazil
inferred← citeshttps://doi.org/10.1093/aob/mch069openalex-snapshot
The North-east-Brazilian Liana, Adenocalymna dichilum (Bignoniaceae) Pollinated by Bats
inferred← citeshttps://doi.org/10.1093/aob/mcl007openalex-snapshot
The Genetic Diversity of Two Brazilian Vellozia (Velloziaceae) with Different Patterns of Spatial Distribution and Pollination Biology
inferred← citeshttps://doi.org/10.1093/aob/mcm206openalex-snapshot
Synchronous Pulsed Flowering: Analysis of the Flowering Phenology in Juncus (Juncaceae)
inferred← citeshttps://doi.org/10.1093/aob/mcp066openalex-snapshot
Reproductive success of non-rewarding Cypripedium japonicum benefits from low spatial dispersion pattern and asynchronous flowering
inferred← citeshttps://doi.org/10.1093/aob/mcp106openalex-snapshot
Pollination syndromes in African Marantaceae
inferred← citeshttps://doi.org/10.1093/aob/mcp191openalex-snapshot
Pollination biology of Eulophia alta (Orchidaceae) in Amazonia: effects of pollinator composition on reproductive success in different populations
inferred← citeshttps://doi.org/10.1093/aobpla/plw033openalex-snapshot
Spatiotemporal strategies that facilitate recruitment in a habitat specialist tree species
inferred← citeshttps://doi.org/10.1093/aobpla/plx023openalex-snapshot
Stigmatic limitations on reproductive success in a paleotropical tree: causes and consequences
inferred← citeshttps://doi.org/10.1093/botlinnean/boz100openalex-snapshot
The role of hummingbirds in the evolution and diversification of Bromeliaceae: unsupported claims and untested hypotheses
inferred← citeshttps://doi.org/10.1093/g3journal/jkab010openalex-snapshot
Genome assemblies for two Neotropical trees: Jacaranda copaia and Handroanthus guayacan
inferred← citeshttps://doi.org/10.1093/jpe/rtv066openalex-snapshot
Marine influence controls plant phenological dynamics in Mediterranean Mexico
inferred← citeshttps://doi.org/10.1098/rspb.2008.0894openalex-snapshot
Neighbourhood density and genetic relatedness interact to determine fruit set and abortion rates in a continuous tropical tree population
inferred← citeshttps://doi.org/10.1098/rstb.2021.0213openalex-snapshot
Some sexual consequences of being a plant
inferred← citeshttps://doi.org/10.1101/2024.11.10.622833openalex-snapshot
Mass flowering and flowering asynchrony characterise a seasonal herbaceous community in the Western Ghats
inferred← citeshttps://doi.org/10.1111/1365-2435.12061openalex-snapshot
Evidence of deterministic assembly according to flowering time in an old‐field plant community
inferred← citeshttps://doi.org/10.1111/1365-2745.70058openalex-snapshot
Diverse associations and proximate effects of weather on Madagascar reproductive phenology
inferred← citeshttps://doi.org/10.1111/1440-1703.1131openalex-snapshot
Tropical phenology: Recent advances and perspectives
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