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Legitimate pollination of the tristylous flowers ofEichhornia azurea (Pontederiaceae) byAncyloscelis gigas bees (Anthophoridae, Apoidea)
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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.1537-2197.1984.tb11992.xopenalex-snapshot
THE DEVELOPMENTAL BASIS OF TRISTYLY IN EICHHORNIA PANICULATA (PONTEDERIACEAE)
inferredcites →https://doi.org/10.1002/j.1537-2197.1996.tb13896.xopenalex-snapshot
Tristyly in the endangered Mascarene Island endemic Hugonia serrata (Linaceae)
inferredcites →https://doi.org/10.1007/bf00317414openalex-snapshot
Pollinator visitation in populations of tristylous Eichhornia paniculata in northeastern Brazil
inferredcites →https://doi.org/10.1016/0304-3770(78)90064-5openalex-snapshot
Floral biology of Eichhornia azurea (Swartz) Kunth (Pontederiaceae)
inferredcites →https://doi.org/10.1038/hdy.1987.91openalex-snapshot
Genetic variation in continental and island populations of Eichhornia paniculata (Pontederiaceae)
inferredcites →https://doi.org/10.1080/0028825x.1979.10432574openalex-snapshot
The biology of heterostyly
inferredcites →https://doi.org/10.1111/j.1095-8312.1985.tb00385.xopenalex-snapshot
Floral trimorphism and monomorphism in continental and island populations of Eichhornia paniculata (Spreng.) Solms. (Pontederiaceae)
inferredcites →https://doi.org/10.1111/j.1095-8312.1989.tb00498.xopenalex-snapshot
Patterns of pollen removal and deposition in tristylous Pontederia cordata L. (Pontederiaceae)
inferredcites →https://doi.org/10.1111/j.1438-8677.1996.tb00580.xopenalex-snapshot
Pollen in Bee‐Flower Relations Some Considerations on Melittophily*
inferredcites →https://doi.org/10.1111/j.1442-1984.1990.tb00191.xopenalex-snapshot
Variation in Outcrossing Rates in Eichhornia paniculata : The Role of Demographic and Reproductive Factors *
inferredcites →https://doi.org/10.1111/j.1469-8137.1983.tb03511.xopenalex-snapshot
TRIMORPHIC INCOMPATIBILITY IN MEXICAN POPULATIONS OF PONTEDERIA SAGITTATA PRESL. (PONTEDERIACEAE)
inferredcites →https://doi.org/10.1111/j.1558-5646.1967.tb00150.xopenalex-snapshot
THE ORIGIN AND EVOLUTIONARY DEVELOPMENT OF HETEROSTYLY IN THE ANGIOSPERMS
inferredcites →https://doi.org/10.1111/j.1558-5646.1979.tb04701.xopenalex-snapshot
THE EVOLUTION AND BREAKDOWN OF TRISTYLY
inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb00418.xopenalex-snapshot
ON THE DARWINIAN HYPOTHESIS OF THE ADAPTIVE SIGNIFICANCE OF TRISTYLY
inferredcites →https://doi.org/10.1111/j.1558-5646.1986.tb05738.xopenalex-snapshot
VARIATION IN THE MATING SYSTEM OFEICHHORNIA PANICULATA(SPRENG.) SOLMS. (PONTEDERIACEAE)
inferredcites →https://doi.org/10.1111/j.1558-5646.1989.tb02591.xopenalex-snapshot
THE DISSOLUTION OF A COMPLEX GENETIC POLYMORPHISM: THE EVOLUTION OF SELF-FERTILIZATION IN TRISTYLOUS EICHHORNIA PANICULATA (PONTEDERIACEAE)
inferredcites →https://doi.org/10.1111/j.1558-5646.1992.tb01983.xopenalex-snapshot
EXPERIMENTAL STUDIES ON THE FUNCTIONAL SIGNIFICANCE OF HETEROSTYLY
inferredcites →https://doi.org/10.1139/b82-115openalex-snapshot
Tristyly in Pontederia cordata (Pontederiaceae)
inferredcites →https://doi.org/10.1139/z88-208openalex-snapshot
Temporal changes in the pollinator fauna of tristylous Pontederia cordata, an aquatic plant
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/10.2307/2389759openalex-snapshot
The Energy Cost of Bee Pollination for Pontederia cordata (Pontederiaceae)
inferredcites →https://doi.org/10.2307/2398798openalex-snapshot
Evolution of Sexual Systems in Flowering Plants
inferredcites →https://doi.org/10.2307/2399363openalex-snapshot
Evolution of Breeding Systems in Eichhornia (Pontederiaceae): A Review
inferredcites →https://doi.org/10.2307/2402967openalex-snapshot
Sexual Reproduction in Eichhornia crassipes (Water Hyacinth). II. Seed Production in Natural Populations
inferredcites →https://doi.org/10.5962/bhl.title.122451openalex-snapshot
The different forms of flowers on plants of the same species
inferredcites →https://doi.org/10.5962/bhl.title.46988openalex-snapshot
The different forms of flowers on plants of the same species, by Charles Darwin.
inferredcites →https://doi.org/10.5962/p.376392openalex-snapshot
A Revision of the Bees of the Genus Melissodes in North and Central America. Part II (Hymenoptera, Apidae)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.4980.3.4zenodo-depositor-declared
A revision of the bee genus Ancyloscelis (Hymenoptera: Apidae) in Argentina
inferred← citeshttps://doi.org/10.1002/edn3.421openalex-snapshot
Environmental variables and species traits as drivers of wild bee pollination in intensive agroecosystems—A metabarcoding approach
inferred← citeshttps://doi.org/10.1007/s00114-024-01912-wopenalex-snapshot
Fields of flowers with few strikes: how oligolectic bees manage their foraging behavior on Calibrachoa elegans (Solanaceae)
inferred← citeshttps://doi.org/10.1007/s00606-004-0246-8openalex-snapshot
Pollination of Campanula rapunculus L. (Campanulaceae): How much pollen flows into pollination and into reproduction of oligolectic pollinators?
inferred← citeshttps://doi.org/10.1007/s00606-009-0170-zopenalex-snapshot
Breeding system of tristylous Eichhornia azurea (Pontederiaceae) in the southern Pantanal, Brazil
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/s00606-013-0764-3openalex-snapshot
Pollination of invasive Eichhornia crassipes (Pontederiaceae) by the introduced honeybee (Apis mellifera L.) in South China
inferred← citeshttps://doi.org/10.1007/s11829-018-9626-9openalex-snapshot
Co-dependency between a specialist Andrena bee and its death camas host, Toxicoscordion paniculatum
inferred← citeshttps://doi.org/10.1007/s11829-024-10102-4openalex-snapshot
Pollination of Blumenbachia catharinensis (Loasaceae)—efficient pollen collection and pollen theft from the stigma by an oligolectic bee
inferred← citeshttps://doi.org/10.1007/s12038-025-00530-6openalex-snapshot
Stonebrood in Argentinian wild bees: A neglected disease?
inferred← citeshttps://doi.org/10.1007/s13592-020-00785-yopenalex-snapshot
A brief review of monolecty in bees and benefits of a broadened definition
inferred← citeshttps://doi.org/10.1007/s40415-016-0258-yopenalex-snapshot
Pollination of Aosa rupestris (Hook.) Weigend (Loasaceae): are stamen movements induced by pollinators?
inferred← citeshttps://doi.org/10.1016/j.bjm.2015.08.001openalex-snapshot
Eichhornia azurea decomposition and the bacterial dynamic: an experimental research
inferred← citeshttps://doi.org/10.1016/j.flora.2005.07.002openalex-snapshot
Pollination in Turnera subulata (Turneraceae): Unilateral reproductive dependence of the narrowly oligolectic bee Protomeliturga turnerae (Hymenoptera, Andrenidae)
inferred← citeshttps://doi.org/10.1016/j.flora.2013.09.005openalex-snapshot
Low legitimate pollen flow in distylic Turnera hermannioides (Passifloraceae) and its consequences on fruit and seed set
inferred← citeshttps://doi.org/10.1046/j.1095-8312.2002.00122.xopenalex-snapshot
Flower-visiting bees and the breakdown of the tristylous breeding system of Eichhornia azurea (Swartz) Kunth (Pontederiaceae)
inferred← citeshttps://doi.org/10.1073/pnas.072588699openalex-snapshot
Origin of a complex key innovation in an obligate insect–plant mutualism
inferred← citeshttps://doi.org/10.1079/cabicompendium.108967openalex-snapshot
Eichhornia azurea (anchored water hyacinth)
inferred← citeshttps://doi.org/10.1080/00173134.2019.1664627openalex-snapshot
First pollen record forAncyloscelis apiformes(Apidae: Emphorini) in Central Amazon
inferred← citeshttps://doi.org/10.1080/00218839.2020.1765489openalex-snapshot
The melittofauna and its floral associations in a natural riparian forest in Buenos Aires province, Argentina
inferred← citeshttps://doi.org/10.1093/aob/mcq077openalex-snapshot
Mutual reproductive dependence of distylic Cordia leucocephala (Cordiaceae) and oligolectic Ceblurgus longipalpis (Halictidae, Rophitinae) in the Caatinga
inferred← citeshttps://doi.org/10.1093/aob/mcu181openalex-snapshot
Floral variation and environmental heterogeneity in a tristylous clonal aquatic of the Pantanal wetlands of Brazil
inferred← citeshttps://doi.org/10.1093/biolinnean/blz193openalex-snapshot
Solitary bee pollinators adjust pollen foraging to the unpredictable flower opening of a species of Petunia (Solanaceae)
inferred← citeshttps://doi.org/10.1111/1365-2745.12179openalex-snapshot
Long‐tongued insects promote disassortative pollen transfer in style‐dimorphic Narcissus papyraceus (Amaryllidaceae)
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2010.01587.xopenalex-snapshot
Obligate association of an oligolectic bee and a seasonal aquatic herb in semi-arid north-eastern Brazil
inferred← citeshttps://doi.org/10.1111/jse.12031openalex-snapshot
Self‐pollination in buds and homostyly in Mussaenda shikokiana ( R ubiaceae), a monomorphic species in a distylous clade
inferred← citeshttps://doi.org/10.1111/plb.13072openalex-snapshot
Specialised protagonists in a plant–pollinator interaction: the pollination of Blumenbachia insignis (Loasaceae)
inferred← citeshttps://doi.org/10.1111/plb.13628openalex-snapshot
Pollen, anther, stamen, and androecium mimicry
inferred← citeshttps://doi.org/10.14393/ufu.di.2020.103openalex-snapshot
Ecologia da polinização e biologia floral de Heteropterys pteropetala A. Juss. (Malpighiaceae) em um Cerrado mineiro
inferred← citeshttps://doi.org/10.1590/2175-7860201667202openalex-snapshot
Quando um visitante floral é um polinizador?
inferred← citeshttps://doi.org/10.1653/024.097.0128openalex-snapshot
Foraging Behavior of Apis Mellifera (Hymenoptera: Apidae) and Lycastrirhyncha Nitens (Diptera: Syrphidae) onPontederia sagittata(Commelinales: Pontederiaceae) on a Disturbed Site
inferred← citeshttps://doi.org/10.1653/024.098.0102openalex-snapshot
Temporal Variation in the Behavior ofApis mellifera(Hymenoptera: Apidae) andLycastrirhyncha nitens(Diptera: Syrphidae) onPontederia sagittata(Commelinales: Pontederiaceae) Inflorescences in Relation to Nectar Availability
inferred← citeshttps://doi.org/10.17129/botsci.201openalex-snapshot
¿Es la disolución evolutiva de la tristilia un proceso frecuente?
inferred← citeshttps://doi.org/10.4236/ajps.2015.63049openalex-snapshot
Reproductive Biology and Herkogamy of Psychotria elata (Rubiaceae), a Distylous Species of the Tropical Rain Forests of Costa Rica
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