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The mating consequences of rewarding vs. deceptive pollination systems: Is there a quantity–quality trade‐off?
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4613-1165-2_13openalex-snapshot
Stylar Polymorphisms and the Evolution of Heterostyly in Narcissus (Amaryllidaceae)
inferredcites →https://doi.org/10.1007/bf00384315openalex-snapshot
A new technique for monitoring pollen flow in orchids
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/10.1007/s00442-005-0254-6openalex-snapshot
Lack of floral nectar reduces self-pollination in a fly-pollinated orchid
inferredcites →https://doi.org/10.1007/s004420050113openalex-snapshot
Evidence for widespread pollen limitation of fruiting success in Cape wildflowers
inferredcites →https://doi.org/10.1007/s00606-003-0106-yopenalex-snapshot
Transfer of pollinaria on birds? feet: a new pollination system in orchids
inferredcites →https://doi.org/10.1007/s00606-005-0343-3openalex-snapshot
Deceptive pollination in two subspecies of Disa spathulata (Orchidaceae) differing in morphology and floral fragrance
inferredcites →https://doi.org/10.1007/s10592-012-0373-7openalex-snapshot
Strong inbreeding depression and local outbreeding depression in the rewarding orchid Gymnadenia conopsea
inferredcites →https://doi.org/10.1007/s11829-011-9169-9openalex-snapshot
How long to stay on a plant: the response of bumblebees to encountered nectar levels
inferredcites →https://doi.org/10.1016/c2009-0-00736-3openalex-snapshot
Principles of Pollination Ecology
inferredcites →https://doi.org/10.1016/j.biocon.2007.06.015openalex-snapshot
Fitness variation and genetic diversity in small, remnant populations of the food deceptive orchid Orchis purpurea
inferredcites →https://doi.org/10.1016/j.sajb.2005.04.002openalex-snapshot
Pollination by long-proboscid flies in the endangered African orchid Disa scullyi
inferredcites →https://doi.org/10.1016/j.sajb.2007.02.162openalex-snapshot
Lack of reward promotes outcrossing: Nectar supplementation experiment with Disa pulchra (Orchidaceae)
inferredcites →https://doi.org/10.1016/j.ympev.2006.08.014openalex-snapshot
A molecular phylogeny for the large African orchid genus Disa
inferredcites →https://doi.org/10.1016/s0003-3472(81)80068-1openalex-snapshot
Optimal foraging in bumblebees: Hunting by expectation
inferredcites →https://doi.org/10.1017/cbo9780511542268.006openalex-snapshot
Floral scent, olfaction, and scent-driven foraging behavior
inferredcites →https://doi.org/10.1017/s1464793105006986openalex-snapshot
Mechanisms and evolution of deceptive pollination in orchids
inferredcites →https://doi.org/10.1038/277294a0openalex-snapshot
Pollen dispersal and optimal outcrossing in Delphinium nelsoni
inferredcites →https://doi.org/10.1038/sj.hdy.6800399openalex-snapshot
Population genetic structure in European populations of Spiranthes romanzoffiana set in the context of other genetic studies on orchids
inferredcites →https://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
inferredcites →https://doi.org/10.1046/j.1095-8339.2003.00157.xopenalex-snapshot
Molecular phylogenetics and evolution of Orchidinae and selected Habenariinae (Orchidaceae)
inferredcites →https://doi.org/10.1046/j.1365-2540.2000.00777.xopenalex-snapshot
Genetic structure in the nonrewarding, bumblebee-pollinated orchid Calypso bulbosa
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The influence of nectar and pollen availability on pollen transfer by individual flowers of oil‐seed rape (Brassica napus) when pollinated by bumblebees (Bombus lapidarius)
inferredcites →https://doi.org/10.1071/9780643090149openalex-snapshot
Monocots: Systematics and Evolution
inferredcites →https://doi.org/10.1086/284922openalex-snapshot
Evolutionary Options for Maximizing Pollen Dispersal of Animal-Pollinated Plants
inferredcites →https://doi.org/10.1086/297041openalex-snapshot
Self- and Cross-Fertilization in Plants. II. The Selection of Self- Fertilization
inferredcites →https://doi.org/10.1086/368347openalex-snapshot
The Evolution of Empty Flowers Revisited
inferredcites →https://doi.org/10.1086/422044openalex-snapshot
Reproductive Success and Sex Variation in Nectarless and Rewarding Orchids
inferredcites →https://doi.org/10.1086/523364openalex-snapshot
Function and Evolution of Aggregated Pollen in Angiosperms
inferredcites →https://doi.org/10.1093/aob/mcn218openalex-snapshot
Reproductive biology of Acrolophia cochlearis (Orchidaceae): estimating rates of cross-pollination in epidendroid orchids
inferredcites →https://doi.org/10.1093/aob/mcq164openalex-snapshot
Differences in pollen viability in relation to different deceptive pollination strategies in Mediterranean orchids
inferredcites →https://doi.org/10.1093/aob/mcu139openalex-snapshot
Desiccation tolerance, longevity and seed-siring ability of entomophilous pollen from UK native orchid species
inferredcites →https://doi.org/10.1093/biomet/73.1.13openalex-snapshot
Longitudinal Data Analysis Using Generalized Linear Models
inferredcites →https://doi.org/10.1098/rsbl.2008.0702openalex-snapshot
Relationships between population size and pollen fates in a moth-pollinated orchid
inferredcites →https://doi.org/10.1098/rsbl.2013.0500openalex-snapshot
Ancestral deceit and labile evolution of nectar production in the African orchid genusDisa
inferredcites →https://doi.org/10.1098/rspb.2001.1705openalex-snapshot
Are there fitness advantages in being a rewardless orchid? Reward supplementation experiments with Barlia robertiana
inferredcites →https://doi.org/10.1098/rspb.2002.2018openalex-snapshot
The potential for floral mimicry in rewardless orchids: an experimental study
inferredcites →https://doi.org/10.1098/rspb.2003.2659openalex-snapshot
The effects of nectar addition on pollen removal and geitonogamy in the non-rewarding orchid Anacamptis morio
inferredcites →https://doi.org/10.1098/rspb.2011.1849openalex-snapshot
Bumble-bee learning selects for both early and long flowering in food-deceptive plants
inferredcites →https://doi.org/10.1098/rstb.2009.0226openalex-snapshot
Floral adaptation and diversification under pollen limitation
inferredcites →https://doi.org/10.1111/1365-2745.12430openalex-snapshot
Nonlinear costs of reproduction in a long‐lived plant
inferredcites →https://doi.org/10.1111/ele.12417openalex-snapshot
Climate‐dependent costs of reproduction: Survival and fecundity costs decline with length of the growing season and summer temperature
inferredcites →https://doi.org/10.1111/j.0014-3820.2000.tb00051.xopenalex-snapshot
OUTBREEDING DEPRESSION VARIES AMONG COHORTS OF IPOMOPSIS AGGREGATA PLANTED IN NATURE
inferredcites →https://doi.org/10.1111/j.1095-8312.2004.00400.xopenalex-snapshot
Variation in sexual reproduction in orchids and its evolutionary consequences: a spasmodic journey to diversification
inferredcites →https://doi.org/10.1111/j.1095-8312.2005.00541.xopenalex-snapshot
Pollen fates and the limits on male reproductive success in an orchid population
inferredcites →https://doi.org/10.1111/j.1095-8339.2009.00985.xopenalex-snapshot
Comparative micromorphology of nectariferous and nectarless labellar spurs in selected clades of subtribe Orchidinae (Orchidaceae)
inferredcites →https://doi.org/10.1111/j.1365-2435.2007.01303.xopenalex-snapshot
Competition for pollinator visitation between deceptive and rewarding artificial inflorescences: an experimental test of the effects of floral colour similarity and spatial mingling
inferredcites →https://doi.org/10.1111/j.1365-2745.2008.01464.xopenalex-snapshot
Multigenerational analysis of spatial structure in the terrestrial, food‐deceptive orchid Orchis mascula
inferredcites →https://doi.org/10.1111/j.1365-294x.2004.02383.xopenalex-snapshot
Mating patterns and gene flow in the neotropical epiphytic orchid, Laelia rubescens
inferredcites →https://doi.org/10.1111/j.1420-9101.2008.01519.xopenalex-snapshot
Inbreeding depression and outbreeding depression in Digitalis purpurea: optimal outcrossing distance in a tetraploid
inferredcites →https://doi.org/10.1111/j.1420-9101.2008.01565.xopenalex-snapshot
Should food‐deceptive species flower before or after rewarding species? An experimental test of pollinator visitation behaviour under contrasting phenologies
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01592.xopenalex-snapshot
Pollinator limitation and inbreeding depression in orchid species with and without nectar rewards
inferredcites →https://doi.org/10.1111/j.1558-5646.1994.tb01366.xopenalex-snapshot
CROSSING‐DISTANCE EFFECTS IN DELPHINIUM NELSONII : OUTBREEDING AND INBREEDING DEPRESSION IN PROGENY FITNESS
inferredcites →https://doi.org/10.1111/j.1558-5646.1996.tb03611.xopenalex-snapshot
ECOLOGICAL AND GENETIC CONSEQUENCES OF POLLINATION BY SEXUAL DECEPTION IN THE ORCHIDCALADENIA TENTACTULATA
inferredcites →https://doi.org/10.1111/j.1558-5646.1997.tb02387.xopenalex-snapshot
LONG-TONGUED FLY POLLINATION AND EVOLUTION OF FLORAL SPUR LENGTH IN THE DISA DRACONIS COMPLEX (ORCHIDACEAE)
inferredcites →https://doi.org/10.1111/j.1558-5646.2011.01515.xopenalex-snapshot
HOW DEPRESSED? ESTIMATES OF INBREEDING EFFECTS DURING SEED DEVELOPMENT DEPEND ON REPRODUCTIVE CONDITIONS
inferredcites →https://doi.org/10.1146/annurev.es.18.110187.001321openalex-snapshot
INBREEDING DEPRESSION AND ITS EVOLUTIONARY CONSEQUENCES
inferredcites →https://doi.org/10.1266/ggs.73.281openalex-snapshot
Spatial genetic structure in populations of Cymbidiumgoeringii(Orchidaceae).
inferredcites →https://doi.org/10.1890/0012-9658(1998)079[2789:tcohtc]2.0.co;2openalex-snapshot
THEORETICAL CONSEQUENCES OF HETEROGENEOUS TRANSPORT CONDITIONS FOR POLLEN DISPERSAL BY ANIMALS
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/10.1890/02-0471openalex-snapshot
POLLINATION SUCCESS IN A DECEPTIVE ORCHID IS ENHANCED BY CO-OCCURRING REWARDING MAGNET PLANTS
inferredcites →https://doi.org/10.2307/1219717openalex-snapshot
The Orchids: Natural History and Classification
inferredcites →https://doi.org/10.2307/1270212openalex-snapshot
Analysis of Messy Data, Volume I: Designed Experiments
inferredcites →https://doi.org/10.2307/1938912openalex-snapshot
Outcrossing Distance Effects in Delphinium Nelsonii: Pollen Loads, Pollen Tubes, and Seed Set
inferredcites →https://doi.org/10.2307/2390078openalex-snapshot
Effects of Flower Number and Position on Self-Fertilization in Experimental Populations of Eichhornia paniculata (Pontederiaceae)
inferredcites →https://doi.org/10.2307/2533558openalex-snapshot
Small Sample Inference for Fixed Effects from Restricted Maximum Likelihood
inferredcites →https://doi.org/10.2307/2992007openalex-snapshot
Pollination Ecology and Maintenance of Species Integrity in Cooccurring Disa racemosa L.f. and Disa venosa SW. (Orchidaceae) in South Africa
inferredcites →https://doi.org/10.2307/3545212openalex-snapshot
Attractiveness to Pollinators: A Plant's Dilemma
inferredcites →https://doi.org/10.3732/ajb.89.10.1579openalex-snapshot
The consequences of rewardlessness in orchids: reward‐supplementation experiments with Anacamptis morio (Orchidaceae)
inferredcites →https://doi.org/10.3732/ajb.91.1.52openalex-snapshot
Spatial genetic structure in populations of the terrestrial orchid Cephalanthera longibracteata (Orchidaceae)
inferredcites →https://doi.org/10.4102/abc.v13i3/4.1324openalex-snapshot
Taxonomic studies in the Disinae. V. A revision of the genus Monadenia
inferredcites →https://doi.org/10.5091/plecevo.2015.914openalex-snapshot
– Reduced fecundity and genetic diversity in small populations of rewarding versus deceptive orchid species: a meta-analysis
inferredcites →https://doi.org/10.5735/085.045.0604openalex-snapshot
Conservation Genetics of the Endangered Terrestrial OrchidPogonia minorin South Korea
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/phytokeys.244.107288zenodo-depositor-declared
Pollen transfer efficiency in Erica depends on type of pollinator
inferred← citeshttps://doi.org/10.1002/ajb2.70117openalex-snapshot
Floral specialization for beetle pollination and its implications for pollen dispersal in an African orchid
inferred← citeshttps://doi.org/10.1007/978-1-4939-7771-0_11openalex-snapshot
Tracking Pollen Fates in Orchid Populations
inferred← citeshttps://doi.org/10.1007/s00709-020-01514-zopenalex-snapshot
Storage of orchid pollinia with varying lipid thermal fingerprints
inferred← citeshttps://doi.org/10.1038/s41598-020-57871-5openalex-snapshot
Pollination Mechanisms are Driving Orchid Distribution in Space
inferred← citeshttps://doi.org/10.1093/botlinnean/boae032openalex-snapshot
Seed quality and germination performance increase with cross-pollination in members of subtribe Orchidinae (Orchidaceae)
inferred← citeshttps://doi.org/10.1098/rspb.2023.1148openalex-snapshot
The economy of pollen dispersal in flowering plants
inferred← citeshttps://doi.org/10.1111/evo.13572openalex-snapshot
Mating consequences of contrasting hermaphroditic plant sexual systems
inferred← citeshttps://doi.org/10.1111/njb.02308openalex-snapshot
Do local conspecific density and floral display size influence fruit set via pollinator visitation in Orchis militaris ?
inferred← citeshttps://doi.org/10.1111/plb.13069openalex-snapshot
A specialised pollination system using nectar‐seeking thynnine wasps in Caladenia nobilis (Orchidaceae)
inferred← citeshttps://doi.org/10.1111/plb.70122openalex-snapshot
Left and right sides are needed: seed development improves when both stigma lobes of Habenaria limprichtii (Orchidaceae) are pollinated
inferred← citeshttps://doi.org/10.1146/annurev-ecolsys-110316-023021openalex-snapshot
The Ecology of Mating and Its Evolutionary Consequences in Seed Plants
inferred← citeshttps://doi.org/10.11575/prism/27645openalex-snapshot
Resource Allocation and Translocation to Sexual Reproduction and Clonal Growth in the Rewardless Orchid Cypripedium parviflorum
inferred← citeshttps://doi.org/10.1186/s12870-021-02968-wopenalex-snapshot
A comparative study on the reproductive success of two rewarding Habenaria species (Orchidaceae) occurring in roadside verge habitats
inferred← citeshttps://doi.org/10.14712/23361964.2021.3openalex-snapshot
Factors determining the distribution of orchids – a review with examples from the Czech Republic
inferred← citeshttps://doi.org/10.14712/23361964.2023.12openalex-snapshot
Pollination strategies of deceptive orchids – a review
inferred← citeshttps://doi.org/10.1556/034.67.2025.4.8openalex-snapshot
Population Performance of Three Orchid Species in a Drying Molinia Caerulea Meadow in Budapest (Hungary)
inferred← citeshttps://doi.org/10.1590/0102-33062018abb0121openalex-snapshot
Flower trade-offs derived from nectar investment in female reproduction of two Nicotiana species (Solanaceae)
inferred← citeshttps://doi.org/10.3390/plants14020204openalex-snapshot
Does Reproductive Success in Orchids Affect the Evolution of Their Number of Flowers?
inferred← citeshttps://doi.org/10.6084/m9.figshare.14451070openalex-snapshot
Additional file 1 of A comparative study on the reproductive success of two rewarding Habenaria species (Orchidaceae) occurring in roadside verge habitats
inferred← citeshttps://doi.org/10.6084/m9.figshare.14451073openalex-snapshot
Additional file 2 of A comparative study on the reproductive success of two rewarding Habenaria species (Orchidaceae) occurring in roadside verge habitats
inferred← citeshttps://doi.org/10.64898/2025.12.05.692704openalex-snapshot
Two hundred years of changes in orchid pollination revealed using herbarium specimens
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