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POLLINATION SUCCESS IN A DECEPTIVE ORCHID IS ENHANCED BY CO-OCCURRING REWARDING MAGNET PLANTS

https://doi.org/10.1890/02-0471
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/j.1537-2197.1987.tb08605.xopenalex-snapshot
INTERPOPULATIONAL VARIATION IN FRUIT PRODUCTION: THE ROLE OF POLLINATION‐LIMITATION IN THE OLYMPIC MOUNTAINS
inferredcites →https://doi.org/10.1002/j.1537-2197.1988.tb14198.xopenalex-snapshot
REPRODUCTIVE SUCCESS AND INFLORESCENCE SIZE OF CALOPOGON TUBEROSUS (ORCHIDACEAE)
inferredcites →https://doi.org/10.1006/bijl.1994.1062openalex-snapshot
Evidence for Batesian mimicry in a butterfly-pollinated orchid
inferredcites →https://doi.org/10.1006/bijl.1999.0430openalex-snapshot
Batesian mimicry in the non-rewarding orchid Disa pulchra, and its consequences for pollinator behaviour
inferredcites →https://doi.org/10.1006/bijl.2000.0510openalex-snapshot
Colour similarity to rewarding model plants affects pollination in a food deceptive orchid, Orchis boryi
inferredcites →https://doi.org/10.1007/bf00317156openalex-snapshot
Plant interactions for pollinator visits: a test of the magnet species effect
inferredcites →https://doi.org/10.1007/bf00317637openalex-snapshot
Habitat dependent pollination success in a Cape orchid
inferredcites →https://doi.org/10.1007/bf00329430openalex-snapshot
Deceptive pollination of Dactylorhiza incarnata: an experimental test of the magnet species hypothesis
inferredcites →https://doi.org/10.1007/bf00329707openalex-snapshot
Floral constancy in bumble bees: handling efficiency or perceptual conditioning?
inferredcites →https://doi.org/10.1007/bf00333945openalex-snapshot
Population size, pollinator visitation and fruit production in the deceptive orchid Calypso bulbosa
inferredcites →https://doi.org/10.1007/bf00349193openalex-snapshot
Floral mimicry between Orchis israelitica Baumann and Dafni (Orchidaceae) and Bellevalia flexuosa Boiss. (Liliaceae)
inferredcites →https://doi.org/10.1007/bf00384485openalex-snapshot
The pollination biology of Calypso bulbosa var. Americana (Orchidaceae): Initial deception of bumblebee visitors
inferredcites →https://doi.org/10.1007/bf00984105openalex-snapshot
The structure and function of orchid pollinaria
inferredcites →https://doi.org/10.1007/bf02071589openalex-snapshot
Effects of variation in inflorescence size and floral rewards on the visitation rates of traplining pollinators ofAralia hispida
inferredcites →https://doi.org/10.1007/bf02912621openalex-snapshot
Positive interactions among plants
inferredcites →https://doi.org/10.1007/s002650000213openalex-snapshot
Color choices by bumble bees ( Bombus terrestris ): innate preferences and generalization after learning
inferredcites →https://doi.org/10.1016/0169-5347(87)90052-8openalex-snapshot
Effects of plant species on each other's pollination: Is community structure influenced?
inferredcites →https://doi.org/10.1016/0169-5347(92)90170-gopenalex-snapshot
Orchid pollination biology
inferredcites →https://doi.org/10.1016/s0167-8809(00)00262-0openalex-snapshot
Site constancy of bumble bees in an experimentally patchy habitat
inferredcites →https://doi.org/10.1016/s1360-1385(99)01445-4openalex-snapshot
Floral mimicry: a fascinating yet poorly understood phenomenon
inferredcites →https://doi.org/10.1038/305799a0openalex-snapshot
Mimesis of bellflower (Campanula) by the red helleborine orchid Cephalanthera rubra
inferredcites →https://doi.org/10.1046/j.1365-2664.1999.00428.xopenalex-snapshot
A landscape‐scale study of bumble bee foraging range and constancy, using harmonic radar
inferredcites →https://doi.org/10.1086/284922openalex-snapshot
Evolutionary Options for Maximizing Pollen Dispersal of Animal-Pollinated Plants
inferredcites →https://doi.org/10.1086/286200openalex-snapshot
Pollinator Behavior and Deceptive Pollination: Learning Process and Floral Evolution
inferredcites →https://doi.org/10.1093/beheco/8.3.239openalex-snapshot
Foraging dynamics of bumble bees: correlates of movements within and between plant species
inferredcites →https://doi.org/10.1111/j.1558-5646.1975.tb00212.xopenalex-snapshot
BEE FLOWERS: A HYPOTHESIS ON FLOWER VARIETY AND BLOOMING TIMES
inferredcites →https://doi.org/10.1111/j.1558-5646.1997.tb03655.xopenalex-snapshot
NEGATIVE FREQUENCY-DEPENDENT SELECTION BY POLLINATORS ON ARTIFICIAL FLOWERS WITHOUT REWARDS
inferredcites →https://doi.org/10.1111/j.1756-1051.1983.tb01059.xopenalex-snapshot
Anthecology of Orchis mascula (Orchidaceae)
inferredcites →https://doi.org/10.1111/j.1756-1051.1986.tb00472.xopenalex-snapshot
The pollination ecology of two nectarless Cimicifuga sp. (Ranunculaceae) in North America
inferredcites →https://doi.org/10.1146/annurev.es.15.110184.001355openalex-snapshot
Mimicry and Deception in Pollination
inferredcites →https://doi.org/10.1146/annurev.es.25.110194.002431openalex-snapshot
THE ECOLOGICAL CONSEQUENCES OF SHARED NATURAL ENEMIES
inferredcites →https://doi.org/10.1890/0012-9658(1998)079[1246:mafpsi]2.0.co;2openalex-snapshot
MALE AND FEMALE POLLINATION SUCCESS IN A DECEPTIVE ORCHID, A SELECTION STUDY
inferredcites →https://doi.org/10.1890/0012-9658(1999)080[2607:pcgate]2.0.co;2openalex-snapshot
POLLEN CARRYOVER, GEITONOGAMY, AND THE EVOLUTION OF DECEPTIVE POLLINATION SYSTEMS IN ORCHIDS
inferredcites →https://doi.org/10.1890/0012-9658(2000)081[1784:aridtp]2.0.co;2openalex-snapshot
ASSOCIATIONAL RESISTANCE: INSECT DAMAGE TO PURPLE LOOSESTRIFE REDUCED IN THICKETS OF SWEET GALE
inferredcites →https://doi.org/10.2307/1938589openalex-snapshot
Floral Neighborhood and Pollination Success in Four Hummingbird‐Pollinated Cloud Forest Plant Species
inferredcites →https://doi.org/10.2307/1939539openalex-snapshot
The Effects of Pathogen‐Induced Pseudoflowers and Buttercups on Each Other's Insect Visitation
inferredcites →https://doi.org/10.2307/1940443openalex-snapshot
Interactions for Pollination among Coflowering Shrubs
inferredcites →https://doi.org/10.2307/1942161openalex-snapshot
Organization of a Plant‐Arthropod Association in Simple and Diverse Habitats: The Fauna of Collards (Brassica Oleracea)
inferredcites →https://doi.org/10.2307/2259728openalex-snapshot
Pollination of Orchis Caspia--A Nectarless Plant which Deceives the Pollinators of Nectariferous Species from other Plant Families
inferredcites →https://doi.org/10.2307/2261535openalex-snapshot
Climatic and Phylogenetic Determinants of Flowering Seasonality in the Cape Flora
inferredcites →https://doi.org/10.2307/2401281openalex-snapshot
Dandelion as a Competitor to Fruit Trees for Bee Visits
inferredcites →https://doi.org/10.2307/2424843openalex-snapshot
Effects of Stand Composition on Insect Visitation in Two-Species Mixtures of Hieracium
inferredcites →https://doi.org/10.2307/3544491openalex-snapshot
Patterns of Visitation by Animal Pollinators
inferredcites →https://doi.org/10.2307/4030openalex-snapshot
Spatial and Temporal Components of Resource Assessment by Flower-Feeding Insects
inferredcites →https://doi.org/10.32473/edis-ep521-2015openalex-snapshot
Orchid Pollination Biology

What points at this work

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

inferred← citeshttps://doi.org/10.3897/natureconservation.56.126919zenodo-depositor-declared
Cymbidium kanran can deceptively attract Apis cerana for free pollination by releasing specialized volatile compounds
inferred← citeshttps://doi.org/10.1002/ajb2.16119openalex-snapshot
An evolutionary framework for understanding habitat partitioning in plants
inferred← citeshttps://doi.org/10.1002/ajb2.16128openalex-snapshot
Analysis of trait–performance–fitness relationships reveals pollinator‐mediated selection on orchid pollination traits
inferred← citeshttps://doi.org/10.1002/ajb2.16198openalex-snapshot
Phenotype–fitness relationships and pollen‐transfer efficiency of five orchid species with different pollination strategies
inferred← citeshttps://doi.org/10.1002/ece3.11233openalex-snapshot
What are the drivers of female success in food‐deceptive orchids?
inferred← citeshttps://doi.org/10.1002/ece3.11295openalex-snapshot
Floral mechanisms promote pollination success and reduce the incidence of self‐pollination in a fly‐pollinated self‐incompatible orchid
inferred← citeshttps://doi.org/10.1002/ece3.1444openalex-snapshot
Experimental evidence that wildflower strips increase pollinator visits to crops
inferred← citeshttps://doi.org/10.1002/ece3.70633openalex-snapshot
Does Climate Change Pose a Threat to the Guild Mimicry System of Australian Orchids?
inferred← citeshttps://doi.org/10.1002/ece3.72843openalex-snapshot
Different Flowering Strategies Ensure Reproductive Success in Two Coexisting Self‐Incompatible Orchids
inferred← citeshttps://doi.org/10.1002/ece3.9759openalex-snapshot
Mimicking orchids lure bees from afar with exaggerated ultraviolet signals
inferred← citeshttps://doi.org/10.1002/ecm.1235openalex-snapshot
The mating consequences of rewarding vs. deceptive pollination systems: Is there a quantity–quality trade‐off?
inferred← citeshttps://doi.org/10.1002/ecs2.4154openalex-snapshot
Removing flowers of a generalist plant changes pollinator visitation, composition, and interaction network structure
inferred← citeshttps://doi.org/10.1002/ecs2.4734openalex-snapshot
Can trait matching inform the design of pollinator‐friendly urban green spaces? A review and synthesis of the literature
inferred← citeshttps://doi.org/10.1002/ecy.2170openalex-snapshot
Achlorophyllous orchid can utilize fungi not only for nutritional demands but also pollinator attraction
inferred← citeshttps://doi.org/10.1002/ecy.3327openalex-snapshot
Unclusterable, underdispersed arrangement of insect‐pollinated plants in pollinator niche space
inferred← citeshttps://doi.org/10.1002/ecy.3495openalex-snapshot
Shared friends counterbalance shared enemies in old forests
inferred← citeshttps://doi.org/10.1002/tax.621007openalex-snapshot
Epidendrum (Orchidaceae) as a model system for ecological and evolutionary studies in the Neotropics
inferred← citeshttps://doi.org/10.1007/978-1-4614-0592-4_1openalex-snapshot
Introduction
inferred← citeshttps://doi.org/10.1007/978-1-4614-0592-4_2openalex-snapshot
Cypripedium L. (The Lady’s-Slippers), Introduction
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Subtribes Goodyerinae and Cranichidinae
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Pollinator Trapping in Carnivorous Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-96397-6_56openalex-snapshot
Pollinator Trapping in Carnivorous Plants
inferred← citeshttps://doi.org/10.1007/978-3-540-89230-4_12openalex-snapshot
Deceptive Behavior in Plants. II. Food Deception by Plants: From Generalized Systems to Specialized Floral Mimicry
inferred← citeshttps://doi.org/10.1007/978-981-92-0096-2_5openalex-snapshot
Pollination Ecology and Conservation Perspectives on Orchid Species in the Western Himalayan Landscape
inferred← citeshttps://doi.org/10.1007/bf02805262openalex-snapshot
Is the colour dimorphism inDactylorhiza sambucina maintained by differential seed viability instead of frequency-dependent selection?
inferred← citeshttps://doi.org/10.1007/s00035-006-0762-yopenalex-snapshot
Fungal pseudoflowers can influence the fecundity of insect-pollinated flowers on Euphorbia cyparissias
inferred← citeshttps://doi.org/10.1007/s00040-023-00934-3openalex-snapshot
Impact of empty flowers on foraging choice and movement within floral patches by the honey bee, Apis mellifera
inferred← citeshttps://doi.org/10.1007/s00114-005-0636-yopenalex-snapshot
On the success of a swindle: pollination by deception in orchids
inferred← citeshttps://doi.org/10.1007/s00114-008-0481-xopenalex-snapshot
Indirect interactions between invasive and native plants via pollinators
inferred← citeshttps://doi.org/10.1007/s00114-021-01771-9openalex-snapshot
Müllerian mimicry between oil-producing orchids and Malpighiaceae? An old hypothesis finally tested
inferred← citeshttps://doi.org/10.1007/s00265-023-03406-7openalex-snapshot
Ecological drivers of bee cognition: insights from stingless bees
inferred← citeshttps://doi.org/10.1007/s00442-004-1693-1openalex-snapshot
Pollinator community structure and sources of spatial variation in plant?pollinator interactions in Clarkia xantiana ssp. xantiana
inferred← citeshttps://doi.org/10.1007/s00442-006-0530-0openalex-snapshot
Experimental investigation of the effect of spatial aggregation on reproductive success in a rewardless orchid
inferred← citeshttps://doi.org/10.1007/s00442-006-0605-yopenalex-snapshot
Pollination niche overlap between a parasitic plant and its host
inferred← citeshttps://doi.org/10.1007/s00442-007-0870-4openalex-snapshot
Impact of floral traits on the reproductive success of epiphytic and terrestrial tropical orchids
inferred← citeshttps://doi.org/10.1007/s00442-008-1033-yopenalex-snapshot
The plot thickens: does low density affect visitation and reproductive success in a perennial herb, and are these effects altered in the presence of a co-flowering species?
inferred← citeshttps://doi.org/10.1007/s00442-009-1346-5openalex-snapshot
Relationships between the floral neighborhood and individual pollen limitation in two self-incompatible herbs
inferred← citeshttps://doi.org/10.1007/s00442-010-1693-2openalex-snapshot
Increased relative abundance of an invasive competitor for pollination, Lythrum salicaria, reduces seed number in Mimulus ringens
inferred← citeshttps://doi.org/10.1007/s00442-010-1879-7openalex-snapshot
Do pollinators influence the assembly of flower colours within plant communities?
inferred← citeshttps://doi.org/10.1007/s00442-011-1987-zopenalex-snapshot
Relative abundance of an invasive alien plant affects native pollination processes
inferred← citeshttps://doi.org/10.1007/s00442-020-04770-1openalex-snapshot
Facilitative pollinator sharing decreases with floral similarity in multiple systems
inferred← citeshttps://doi.org/10.1007/s00442-021-05095-3openalex-snapshot
Pollinator-mediated facilitation alleviates pollen limitation in a plant–hummingbird network
inferred← citeshttps://doi.org/10.1007/s00442-026-05943-0openalex-snapshot
Honeydew-mediated indirect interactions: magnet and spillover effects of an invasive willow–aphid complex
inferred← citeshttps://doi.org/10.1007/s00468-023-02480-8openalex-snapshot
The scaling relationship between perianth fresh mass and area: proof of concept using Magnolia × soulangeana Soul.-Bod
inferred← citeshttps://doi.org/10.1007/s00468-025-02645-7openalex-snapshot
Testing the validity of the Montgomery–Koyama–Smith equation and the power law equation using 3231 tepals of a Magnolia species
inferred← citeshttps://doi.org/10.1007/s00606-004-0248-6openalex-snapshot
Effects of local density and flower colour polymorphism on pollination and reproduction in the rewardless orchid Dactylorhiza sambucina (L.) So�
inferred← citeshttps://doi.org/10.1007/s00606-005-0338-0openalex-snapshot
Pollination success in monochromic yellow populations of the rewardless orchid Dactylorhiza sambucina
inferred← citeshttps://doi.org/10.1007/s00606-006-0503-0openalex-snapshot
Increase of pollinator attraction by means of a visual signal in the sexually deceptive orchid, Ophrys heldreichii (Orchidaceae)
inferred← citeshttps://doi.org/10.1007/s00606-006-0507-9openalex-snapshot
Pollination of the European food-deceptive Traunsteinera globosa (Orchidaceae): the importance of nectar-producing neighbouring plants
inferred← citeshttps://doi.org/10.1007/s00606-011-0473-8openalex-snapshot
Floral display influences male and female reproductive success of the deceptive orchid Phaius delavayi
inferred← citeshttps://doi.org/10.1007/s00606-011-0477-4openalex-snapshot
Factors affecting pollinator movement and plant fitness in a specialized pollination system
inferred← citeshttps://doi.org/10.1007/s00606-015-1276-0openalex-snapshot
Pollinators can prefer rewarding models to mimics: consequences for the assumptions of Batesian floral mimicry
inferred← citeshttps://doi.org/10.1007/s00606-020-01709-0openalex-snapshot
How do rewardless Bletilla striata flowers attract pollinators to achieve pollination?
inferred← citeshttps://doi.org/10.1007/s10265-015-0716-9openalex-snapshot
Pollination system and the effect of inflorescence size on fruit set in the deceptive orchid Cephalanthera falcata
inferred← citeshttps://doi.org/10.1007/s10265-016-0853-9openalex-snapshot
Who helps whom? Pollination strategy of Iris tuberosa and its relationship with a sexually deceptive orchid
inferred← citeshttps://doi.org/10.1007/s10530-019-02130-6openalex-snapshot
Effects of invasive Cirsium arvense on pollination in a southern Appalachian floral community vary with spatial scale and floral symmetry
inferred← citeshttps://doi.org/10.1007/s10530-021-02519-2openalex-snapshot
An exotic magnet plant alters pollinator abundance and behavior: a field test with a native mistletoe
inferred← citeshttps://doi.org/10.1007/s10530-024-03442-yopenalex-snapshot
Invasions of the bamboo orchid: performance variability on islands oceans apart
inferred← citeshttps://doi.org/10.1007/s10682-022-10174-9openalex-snapshot
Are some species ‘robust’ to exploitation? Explaining persistence in deceptive relationships
inferred← citeshttps://doi.org/10.1007/s10841-016-9904-8openalex-snapshot
Pollinator conservation at the local scale: flower density, diversity and community structure increase flower visiting insect activity to mixed floral stands
inferred← citeshttps://doi.org/10.1007/s11258-008-9543-6openalex-snapshot
Reproductive success in the Mexican rewardless Oncidium cosymbephorum (Orchidaceae) facilitated by the oil-rewarding Malpighia glabra (Malpighiaceae)
inferred← citeshttps://doi.org/10.1007/s11258-011-9915-1openalex-snapshot
Effects of conspecific and heterospecific floral density on the pollination of two related rewarding orchids
inferred← citeshttps://doi.org/10.1007/s11258-012-0113-6openalex-snapshot
Short-term fitness and long-term population trends in the orchid Anacamptis morio
inferred← citeshttps://doi.org/10.1007/s11258-018-0868-5openalex-snapshot
Facilitative interactions among co-flowering Primula species mediated by pollinator sharing
inferred← citeshttps://doi.org/10.1007/s11258-018-0875-6openalex-snapshot
Intersexual mimicry and flowering phenology facilitate pollination in a dioecious habitat specialist species, Myristica fatua (Myristicaceae)
inferred← citeshttps://doi.org/10.1007/s11258-022-01221-0openalex-snapshot
Preventing inbreeding depression in Anacamptis coriophora (Orchidaceae) as a model of food-rewarding orchid
inferred← citeshttps://doi.org/10.1007/s11284-013-1116-zopenalex-snapshot
An investigation of temporal flowering segregation in species‐rich grasslands
inferred← citeshttps://doi.org/10.1007/s11284-017-1501-0openalex-snapshot
Are food‐deceptive orchid species really functionally specialized for pollinators?
inferred← citeshttps://doi.org/10.1007/s11284-018-1572-6openalex-snapshot
Pollinator trapping in selfing carnivorous plants, Drosera makinoi and D. toyoakensis (Droseraceae)
inferred← citeshttps://doi.org/10.1007/s11829-008-9051-6openalex-snapshot
Carry-over effects of bumblebee associative learning in changing plant communities leads to increased costs of foraging
inferred← citeshttps://doi.org/10.1007/s11829-011-9122-yopenalex-snapshot
Variable responses of hawkmoths to nectar-depleted plants in two native Petunia axillaris (Solanaceae) populations
inferred← citeshttps://doi.org/10.1007/s11829-024-10096-zopenalex-snapshot
Flowering phenology patterns promotes pollination facilitation in coexisting Anthurium species from a mountain forest in Colombia
inferred← citeshttps://doi.org/10.1007/s11829-026-10226-9openalex-snapshot
Metal pollution and floral abundance influence the diversity of flower visiting insects
inferred← citeshttps://doi.org/10.1007/s12080-017-0333-4openalex-snapshot
Neutral hybridization can overcome a strong Allee effect by improving pollination quality
inferred← citeshttps://doi.org/10.1007/s12229-010-9047-7openalex-snapshot
Biotic Resource Needs of Specialist Orchid Pollinators
inferred← citeshttps://doi.org/10.1007/s13592-023-00997-yopenalex-snapshot
Flower choice by the stingless bee Tetragonula carbonaria is not influenced by colour-similarity to a higher-reward flower in the same patch
inferred← citeshttps://doi.org/10.1007/s42974-021-00056-5openalex-snapshot
Indirect facilitation mediated by pollinators in intermountain prairie
inferred← citeshttps://doi.org/10.1016/j.actao.2008.01.001openalex-snapshot
Effect of nectar supplementation on male and female components of pollination success in the deceptive orchid Dactylorhiza sambucina
inferred← citeshttps://doi.org/10.1016/j.actao.2008.04.007openalex-snapshot
The effects of plant density and nectar reward on bee visitation to the endangered orchid Spiranthes romanzoffiana
inferred← citeshttps://doi.org/10.1016/j.actao.2011.04.005openalex-snapshot
Do alpine plants facilitate each other’s pollination? Experiments at a small spatial scale
inferred← citeshttps://doi.org/10.1016/j.actao.2014.01.001openalex-snapshot
Pollination ecology of a plant in its native and introduced areas
inferred← citeshttps://doi.org/10.1016/j.actao.2020.103605openalex-snapshot
Orchid-pollinator network in Euro-Mediterranean region: What we know, what we think we know, and what remains to be done
inferred← citeshttps://doi.org/10.1016/j.actao.2025.104077openalex-snapshot
Competition for resources: What factors lead honey bees to outcompete other insect competitors?
inferred← citeshttps://doi.org/10.1016/j.agee.2016.02.019openalex-snapshot
Mass flowering crops in a patchy agricultural landscape can reduce bee abundance in adjacent shrublands
inferred← citeshttps://doi.org/10.1016/j.agee.2017.09.002openalex-snapshot
Exotic plants growing in crop field margins provide little support to mango crop flower visitors
inferred← citeshttps://doi.org/10.1016/j.anbehav.2008.08.010openalex-snapshot
Inadvertent social information in foraging bumblebees: effects of flower distribution and implications for pollination
inferred← citeshttps://doi.org/10.1016/j.baae.2014.12.005openalex-snapshot
Distance-dependent effects of invasive Lupinus polyphyllus on pollination and reproductive success of two native herbs
inferred← citeshttps://doi.org/10.1016/j.baae.2018.12.003openalex-snapshot
Are there magnet plants in Australian ecosystems: Pollinator visits to neighbouring plants are not affected by proximity to mass flowering plants
inferred← citeshttps://doi.org/10.1016/j.baae.2021.04.013openalex-snapshot
Shrub canopy matrix decreases reproductive output of a sheltered plant via pollinator exclusion
inferred← citeshttps://doi.org/10.1016/j.biocon.2007.04.015openalex-snapshot
Do alien plant invasions really affect pollination success in native plant species?
inferred← citeshttps://doi.org/10.1016/j.biocon.2013.11.027openalex-snapshot
Specialized ecological interactions and plant species rarity: The role of pollinators and mycorrhizal fungi across multiple spatial scales
inferred← citeshttps://doi.org/10.1016/j.bse.2019.05.005openalex-snapshot
Chemical composition of floral scents from three Plumeria rubra L. (Apocynaceae) forms linked to petal color proprieties
inferred← citeshttps://doi.org/10.1016/j.cois.2016.03.007openalex-snapshot
Olfaction in context — sources of nuance in plant–pollinator communication
inferred← citeshttps://doi.org/10.1016/j.cris.2024.100091openalex-snapshot
Predation risk and floral rewards: How pollinators balance these conflicts and the consequences on plant fitness
inferred← citeshttps://doi.org/10.1016/j.ecochg.2021.100043openalex-snapshot
Pollinator-mediated reproductive consequences of altered co-flowering under climate change conditions depend on abiotic context
inferred← citeshttps://doi.org/10.1016/j.ecocom.2022.101003openalex-snapshot
Drivers of plant individual-based pollinator visitation network topology in an arid ecosystem
inferred← citeshttps://doi.org/10.1016/j.flora.2012.07.005openalex-snapshot
Reproductive fitness, population size and genetic variation in Muscari tenuiflorum (Hyacinthaceae): The role of temporal variation
inferred← citeshttps://doi.org/10.1016/j.flora.2016.04.003openalex-snapshot
Does flowering synchrony contribute to the sustainment of dry grassland biodiversity?
inferred← citeshttps://doi.org/10.1016/j.flora.2016.11.013openalex-snapshot
Effects of pollen origin on apomixis in Zygopetalum mackayi orchids
inferred← citeshttps://doi.org/10.1016/j.gecco.2021.e01939openalex-snapshot
The future of a montane orchid species and the impact of climate change on the distribution of its pollinators and magnet species
inferred← citeshttps://doi.org/10.1016/j.jarmap.2020.100286openalex-snapshot
Identification of ecological factors affecting the occurrence and abundance of Dactylorhiza hatagirea (D.Don) Soo in the Himalaya
inferred← citeshttps://doi.org/10.1016/j.jnc.2025.126848openalex-snapshot
The effect of fire on the female pollination success of two non-rewarding orchid species
inferred← citeshttps://doi.org/10.1016/j.jtbi.2017.04.011openalex-snapshot
How to be a good neighbour: Facilitation and competition between two co-flowering species
inferred← citeshttps://doi.org/10.1016/j.jtbi.2023.111609openalex-snapshot
Batesian mimicry or general food deception? An evolutionary game between plants for pollinator services
inferred← citeshttps://doi.org/10.1016/j.pbi.2007.11.003openalex-snapshot
The evolution of floral gigantism
inferred← citeshttps://doi.org/10.1016/j.phytochem.2011.02.005openalex-snapshot
Colour-scent associations in a tropical orchid: Three colours but two odours
inferred← citeshttps://doi.org/10.1016/j.pld.2025.06.008openalex-snapshot
We are not all the same: The role of intrapopulation trait variability in shaping functional strategy and performance of widespread species
inferred← citeshttps://doi.org/10.1016/j.ppees.2015.04.002openalex-snapshot
Biological flora of Central Europe: Dactylorhiza sambucina (L.) Soó
inferred← citeshttps://doi.org/10.1016/j.ppees.2018.12.003openalex-snapshot
Finding the bees knees: A conceptual framework and systematic review of the mechanisms of pollinator-mediated facilitation
inferred← citeshttps://doi.org/10.1016/j.sajb.2022.02.018openalex-snapshot
Colour similarity to flowering neighbours promotes pollinator visits, pollen receipt and maternal fitness
inferred← citeshttps://doi.org/10.1016/j.tplants.2010.09.006openalex-snapshot
Reconnecting plants and pollinators: challenges in the restoration of pollination mutualisms
inferred← citeshttps://doi.org/10.1016/j.tplants.2020.03.009openalex-snapshot
Niche Perspectives on Plant–Pollinator Interactions
inferred← citeshttps://doi.org/10.1016/j.tree.2007.11.003openalex-snapshot
Plant–pollinator interactions and the assembly of plant communities
inferred← citeshttps://doi.org/10.1016/j.tree.2009.06.006openalex-snapshot
Deception in plants: mimicry or perceptual exploitation?
inferred← citeshttps://doi.org/10.1016/j.tree.2010.03.004openalex-snapshot
Floral evolution as a figment of the imagination of pollinators
inferred← citeshttps://doi.org/10.1016/j.tree.2010.04.003openalex-snapshot
Communication theory and the form of receiver-mediated selection
inferred← citeshttps://doi.org/10.1016/j.ympev.2015.04.019openalex-snapshot
Putative floral brood-site mimicry, loss of autonomous selfing, and reduced vegetative growth are significantly correlated with increased diversification in Asarum (Aristolochiaceae)
inferred← citeshttps://doi.org/10.1017/cbo9781139014113.008openalex-snapshot
Pollinator mediated floral divergence in the absence of pollinator shifts
inferred← citeshttps://doi.org/10.1017/cbo9781139014113.015openalex-snapshot
Pollinators as drivers of plant distribution and assemblage into communities
inferred← citeshttps://doi.org/10.1017/cbo9781139014113.016openalex-snapshot
Effects of alien species on plant–pollinator interactions: how can native plants adapt to changing pollination regimes?
inferred← citeshttps://doi.org/10.1017/s0266467411000289openalex-snapshot
Flower number and distance to neighbours affect the fecundity of Goetzea elegans (Solanaceae)
inferred← citeshttps://doi.org/10.1017/s0266467411000411openalex-snapshot
Sapromyiophily in the native orchid, Bulbophyllum variegatum, on Réunion (Mascarene Archipelago, Indian Ocean)
inferred← citeshttps://doi.org/10.1017/s0266467412000508openalex-snapshot
Spatial association between floral resources and hummingbird activity in a Mexican tropical montane cloud forest
inferred← citeshttps://doi.org/10.1017/s1464793105006731openalex-snapshot
Pollen and seed dispersal among dispersed plants
inferred← citeshttps://doi.org/10.1017/s1464793105006986openalex-snapshot
Mechanisms and evolution of deceptive pollination in orchids
inferred← citeshttps://doi.org/10.1038/s41598-019-43553-4openalex-snapshot
Experimental loss of generalist plants reveals alterations in plant-pollinator interactions and a constrained flexibility of foraging
inferred← citeshttps://doi.org/10.1038/s41598-020-57871-5openalex-snapshot
Pollination Mechanisms are Driving Orchid Distribution in Space
inferred← citeshttps://doi.org/10.1038/s41598-021-01611-wopenalex-snapshot
Pollination success increases with plant diversity in high-Andean communities
inferred← citeshttps://doi.org/10.1046/j.1095-8312.2003.00236.xopenalex-snapshot
Experimental and phylogenetic evidence for floral mimicry in a guild of fly-pollinated plants
inferred← citeshttps://doi.org/10.1055/s-2007-965614openalex-snapshot
Floral Scent in Food‐Deceptive Orchids: Species Specificity and Sources of Variability
inferred← citeshttps://doi.org/10.1071/bt08154openalex-snapshot
Implications of pollination by food and sexual deception for pollinator specificity, fruit set, population genetics and conservation of Caladenia (Orchidaceae)
inferred← citeshttps://doi.org/10.1071/wf15172openalex-snapshot
Fire effects on pollination in a sexually deceptive orchid
inferred← citeshttps://doi.org/10.1073/pnas.1714414114openalex-snapshot
In situ modeling of multimodal floral cues attracting wild pollinators across environments
inferred← citeshttps://doi.org/10.1080/07352680802205631openalex-snapshot
Interspecific Pollen Transfer: Magnitude, Prevalence and Consequences for Plant Fitness
inferred← citeshttps://doi.org/10.1080/10549811.2014.973609openalex-snapshot
Fire and Canopy Removal Effects on Demography and Reproduction in Turkeybeard (Xerophyllum asphodeloides), a Fire-Dependent Temperate Forest Herb
inferred← citeshttps://doi.org/10.1080/11263504.2019.1610110openalex-snapshot
Disentangling the pollination system of the food-deceptive orchid Anacamptis longicornu (Orchidaceae): from breeding system to spatio-temporal variation in reproductive success
inferred← citeshttps://doi.org/10.1080/12538078.2014.895419openalex-snapshot
Reproductive biology and colour polymorphism in the food-deceptiveIris lutescens(Iridaceae)
inferred← citeshttps://doi.org/10.1080/14888386.2023.2179112openalex-snapshot
The power of sister crops: intercropping courgette and common bean changes floral morphology and increases diversity of flower visitors
inferred← citeshttps://doi.org/10.1080/17550874.2023.2270992openalex-snapshot
Influence of distance from conspecific and heterospecific co-flowering plants on pollination and fecundity in the nectarless orchid Dactylorhiza sambucina
inferred← citeshttps://doi.org/10.1080/17550874.2024.2412589openalex-snapshot
The deceptive pollination of Anacamptis morio : generalised food deception or an initial step towards adaptive mimicry?
inferred← citeshttps://doi.org/10.1080/23818107.2021.1893215openalex-snapshot
Co-pollination, constancy, and efficiency over time: small beetles and the reproductive success of Acrocomia aculeata (Arecaceae) in the Colombian Orinoquia
inferred← citeshttps://doi.org/10.1086/378539openalex-snapshot
Trumpet Flowers of the Sonoran Desert: Floral Biology ofPeniocereusCacti and SacredDatura
inferred← citeshttps://doi.org/10.1086/507651openalex-snapshot
Do Pollination Syndromes Partition the Pollinator Community? A Test Using Four Sympatric Morning Glory Species
inferred← citeshttps://doi.org/10.1086/511960openalex-snapshot
Positive Indirect Interactions between Neighboring Plant Species via a Lizard Pollinator
inferred← citeshttps://doi.org/10.1086/518255openalex-snapshot
Fruit Removal in the Forest HerbActaea spicataDepends on Local Context of Fruits Sharing the Same Dispersers
inferred← citeshttps://doi.org/10.1086/673858openalex-snapshot
Pollinator Deception in the Orchid Mantis
inferred← citeshttps://doi.org/10.1086/674991openalex-snapshot
A Conceptual Framework for Associational Effects: When Do Neighbors Matter and How Would We Know?
inferred← citeshttps://doi.org/10.1086/684433openalex-snapshot
Inaccurate Color Discrimination by Pollinators Promotes Evolution of Discrete Color Polymorphism in Food-Deceptive Flowers
inferred← citeshttps://doi.org/10.1086/705589openalex-snapshot
Intraspecific Variation in Floral Color and Odor in Orchids
inferred← citeshttps://doi.org/10.1086/705607openalex-snapshot
Differences in Flowering Phenology Are Likely Not the Product of Competition for Pollination inClarkiaCommunities
inferred← citeshttps://doi.org/10.1086/707863openalex-snapshot
Pollinators, Herbivores, and Plant Neighborhood Effects
inferred← citeshttps://doi.org/10.1086/712378openalex-snapshot
Mechanisms of Male-Male Interference during Dispersal of Orchid Pollen
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198732693.001.0001openalex-snapshot
Floral Mimicry
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198732693.002.0003openalex-snapshot
Copyright Page
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198732693.002.0004openalex-snapshot
Dedication
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198732693.002.0005openalex-snapshot
Preface
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198732693.003.0001openalex-snapshot
Introduction
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198732693.003.0002openalex-snapshot
The evolution and maintenance of floral rewardlessness
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198732693.003.0003openalex-snapshot
Generalized food deception
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198732693.003.0004openalex-snapshot
Batesian food-source mimicry
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198732693.003.0005openalex-snapshot
Sexual mimicry
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198732693.003.0006openalex-snapshot
Oviposition-site mimicry
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198732693.003.0007openalex-snapshot
Special cases
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198732693.003.0008openalex-snapshot
Future directions in floral mimicry research
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198732693.003.0009openalex-snapshot
Epilogue
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199228973.001.0001openalex-snapshot
Community Ecology
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.001.0001openalex-snapshot
Biodiversity, Ecosystem Functioning, and Human Wellbeing
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.002.0003openalex-snapshot
Copyright Page
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.002.0005openalex-snapshot
Contributors
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.002.0006openalex-snapshot
Preface
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0001openalex-snapshot
Introduction: the ecological and social implications of changing biodiversity. An overview of a decade of biodiversity and ecosystem functioning research
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0002openalex-snapshot
Consequences of species loss for ecosystem functioning: meta-analyses of data from biodiversity experiments
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0003openalex-snapshot
Biodiversity-ecosystem function research and biodiversity futures: early bird catches the worm or a day late and a dollar short?
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0004openalex-snapshot
A functional guide to functional diversity measures
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0005openalex-snapshot
Forecasting decline in ecosystem services under realistic scenarios of extinction
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0006openalex-snapshot
Biodiversity and the stability of ecosystem functioning
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0007openalex-snapshot
The analysis of biodiversity experiments: from pattern toward mechanism
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0008openalex-snapshot
Towards a food web perspective on biodiversity and ecosystem functioning
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0009openalex-snapshot
Microbial biodiversity and ecosystem functioning under controlled conditions and in the wild
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0010openalex-snapshot
Biodiversity as spatial insurance: the effects of habitat fragmentation and dispersal on ecosystem functioning
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0011openalex-snapshot
Incorporating biodiversity in climate change mitigation initiatives
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0012openalex-snapshot
Restoring biodiversity and ecosystem function: will an integrated approach improve results?
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0013openalex-snapshot
Managed ecosystems: biodiversity and ecosystem functions in landscapes modified by human use
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0014openalex-snapshot
Understanding the role of species richness for crop pollination services
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0015openalex-snapshot
Biodiversity and ecosystem function: perspectives on disease
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0016openalex-snapshot
Opening communities to colonization – the impacts of invaders on biodiversity and ecosystem functioning
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0017openalex-snapshot
The economics of biodiversity and ecosystem services
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0018openalex-snapshot
The valuation of ecosystem services
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0019openalex-snapshot
Modelling biodiversity and ecosystem services in coupled ecological–economic systems
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0020openalex-snapshot
TraitNet: furthering biodiversity research through the curation, discovery, and sharing of species trait data
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199547951.003.0021openalex-snapshot
Can we predict the effects of global change on biodiversity loss and ecosystem functioning?
inferred← citeshttps://doi.org/10.1093/aob/mcaa093openalex-snapshot
Orchid conservation: from theory to practice
inferred← citeshttps://doi.org/10.1093/aob/mcab088openalex-snapshot
A bee’s eye view of remarkable floral colour patterns in the south-west Australian biodiversity hotspot revealed by false colour photography
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/mcq210openalex-snapshot
Reproductive isolation and pollination success of rewarding Galearis diantha and non-rewarding Ponerorchis chusua (Orchidaceae)
inferred← citeshttps://doi.org/10.1093/aob/mcr216openalex-snapshot
The presence of co-flowering species facilitates reproductive success of Pedicularis monbeigiana (Orobanchaceae) through variation in bumble-bee foraging behaviour
inferred← citeshttps://doi.org/10.1093/aob/mct228openalex-snapshot
Pollination in a patchily distributed lousewort is facilitated by presence of a co-flowering plant due to enhancement of quantity and quality of pollinator visits
inferred← citeshttps://doi.org/10.1093/aob/mcy120openalex-snapshot
Effects of spatial patterning of co-flowering plant species on pollination quantity and purity
inferred← citeshttps://doi.org/10.1093/aob/mcz003openalex-snapshot
Deceptive strategy in Dactylorhiza orchids: multidirectional evolution of floral chemistry
inferred← citeshttps://doi.org/10.1093/aob/mcz043openalex-snapshot
Floral colour structure in two Australian herbaceous communities: it depends on who is looking
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