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Pollination of Trichosalpinx (Orchidaceae: Pleurothallidinae) by biting midges (Diptera: Ceratopogonidae)
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Contact sex signals on web and cuticle ofTegenaria atrica (Araneae, Agelenidae)
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DIAGNOSTIC ANATOMICAL CHARACTERS IN THE PLEUROTHALLIDINAE (ORCHIDACEAE)
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ULTRASTRUCTURE OF OSMOPHORES IN RESTREPIA (ORCHIDACEAE)
inferredcites →https://doi.org/10.1002/tax.603016openalex-snapshot
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inferredcites →https://doi.org/10.1006/anbo.1999.0975openalex-snapshot
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inferredcites →https://doi.org/10.1006/anbo.2001.1434openalex-snapshot
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inferredcites →https://doi.org/10.1007/bf00306214openalex-snapshot
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inferredcites →https://doi.org/10.1007/bf02036201openalex-snapshot
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inferredcites →https://doi.org/10.1007/s00606-009-0212-6openalex-snapshot
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inferredcites →https://doi.org/10.1007/s00606-010-0294-1openalex-snapshot
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inferredcites →https://doi.org/10.1007/s00606-014-1100-2openalex-snapshot
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Ceropegia sandersonii Mimics Attacked Honeybees to Attract Kleptoparasitic Flies for Pollination
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inferredcites →https://doi.org/10.1023/a:1021474820601openalex-snapshot
Chemical Polymorphism of the Cuticular Lipids of the Cabbage White Pieris rapae
inferredcites →https://doi.org/10.1038/nature06039openalex-snapshot
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The Flowering of Australia's Rainforests
inferredcites →https://doi.org/10.1071/bt15177openalex-snapshot
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inferredcites →https://doi.org/10.1073/pnas.0406166101openalex-snapshot
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inferredcites →https://doi.org/10.1080/001731300300045247openalex-snapshot
Pollen morphology of the subtribe Pleurothallidinae Lindl. (Orchidaceae)
inferredcites →https://doi.org/10.1080/09670877809414251openalex-snapshot
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Did Pollination Shifts Drive Diversification in Southern African Gladiolus? Evaluating the Model of Pollinator-Driven Speciation
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Lip Anatomy and its Implications for the Pollination Mechanisms of Bulbophyllum Species (Orchidaceae)
inferredcites →https://doi.org/10.1093/aob/mci090openalex-snapshot
Pseudocopulatory Pollination in Lepanthes (Orchidaceae: Pleurothallidinae) by Fungus Gnats
inferredcites →https://doi.org/10.1093/aob/mcp072openalex-snapshot
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inferredcites →https://doi.org/10.1093/aob/mct248openalex-snapshot
Pollinator shifts as triggers of speciation in painted petal irises (Lapeirousia: Iridaceae)
inferredcites →https://doi.org/10.1093/aob/mct295openalex-snapshot
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inferredcites →https://doi.org/10.1093/aob/mcu153openalex-snapshot
Labellar anatomy and secretion in Bulbophyllum Thouars (Orchidaceae: Bulbophyllinae) sect. Racemosae Benth. & Hook. f.
inferredcites →https://doi.org/10.1093/aob/mcv086openalex-snapshot
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inferredcites →https://doi.org/10.1093/aobpla/plu003openalex-snapshot
Floral specialization and angiosperm diversity: phenotypic divergence, fitness trade-offs and realized pollination accuracy
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Exploration of a rare population of Chinese chestnut in North America: stand dynamics, health and genetic relationships
inferredcites →https://doi.org/10.1093/oso/9780198507123.001.0001openalex-snapshot
Genera Orchidacearum
inferredcites →https://doi.org/10.1098/rsif.2012.0847openalex-snapshot
Buckling as an origin of ordered cuticular patterns in flower petals
inferredcites →https://doi.org/10.1098/rspb.2003.2659openalex-snapshot
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inferredcites →https://doi.org/10.1098/rspb.2013.0960openalex-snapshot
Convergent evolution of floral signals underlies the success of Neotropical orchids
inferredcites →https://doi.org/10.1098/rspb.2015.1553openalex-snapshot
Orchid phylogenomics and multiple drivers of their extraordinary diversification
inferredcites →https://doi.org/10.1098/rstb.2009.0243openalex-snapshot
The pollination niche and its role in the diversification and maintenance of the southern African flora
inferredcites →https://doi.org/10.1111/boj.12168openalex-snapshot
Recurrent polymorphic mating type variation in MadagascanBulbophyllumspecies (Orchidaceae) exemplifies a high incidence of auto-pollination in tropical orchids
inferredcites →https://doi.org/10.1111/boj.12176openalex-snapshot
What do floral anatomy and micromorphology tell us about Neotropical Bulbophyllum section Didactyle (Orchidaceae: Bulbophyllinae)?
inferredcites →https://doi.org/10.1111/boj.12253openalex-snapshot
Comparative floral micromorphology and anatomy of species ofBulbophyllumsectionNapelli(Orchidaceae), a Neotropical section widely distributed in forest habitats
inferredcites →https://doi.org/10.1111/boj.12315openalex-snapshot
Diverse labellar secretions in AfricanBulbophyllum(Orchidaceae: Bulbophyllinae) sectionsPtiloglossum,OreonastesandMegaclinium
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.1095-8339.1982.tb00357.xopenalex-snapshot
An annotated check-list of the Pteridophyta of Ceylon
inferredcites →https://doi.org/10.1111/j.1365-3113.1990.tb00311.xopenalex-snapshot
A revision of the Holarctic species of Serromyia Meigen (Diptera: Ceratopogonidae)
inferredcites →https://doi.org/10.1111/j.1442-1984.2010.00277.xopenalex-snapshot
Occurrence of different sites of self‐incompatibility reaction in four Anathallis (Orchidaceae, Pleurothallidinae) species
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01845.xopenalex-snapshot
The chemical nature of fetid floral odours in stapeliads (Apocynaceae‐Asclepiadoideae‐Ceropegieae)
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03292.xopenalex-snapshot
Using phylogenetics to detect pollinator‐mediated floral evolution
inferredcites →https://doi.org/10.1111/j.1558-5646.2008.00327.xopenalex-snapshot
THE ROLE OF POLLINATOR SHIFTS IN THE FLORAL DIVERSIFICATION OF IOCHROMA (SOLANACEAE)
inferredcites →https://doi.org/10.1111/j.1558-5646.2008.00463.xopenalex-snapshot
NATURAL SELECTION REINFORCES SPECIATION IN A RADIATION OF NEOTROPICAL RAINFOREST PLANTS
inferredcites →https://doi.org/10.1111/j.1744-7429.1999.tb00142.xopenalex-snapshot
A Nectar Reward: Is More Better?1
inferredcites →https://doi.org/10.1111/nph.13210openalex-snapshot
The betrayed thief – the extraordinary strategy of A ristolochia rotunda to deceive its pollinators
inferredcites →https://doi.org/10.1111/nph.13855openalex-snapshot
Disentangling visual and olfactory signals in mushroom‐mimicking Dracula orchids using realistic three‐dimensional printed flowers
inferredcites →https://doi.org/10.1111/nph.14629openalex-snapshot
Recent origin and rapid speciation of Neotropical orchids in the world's richest plant biodiversity hotspot
inferredcites →https://doi.org/10.1136/jcp.34.12.1406-copenalex-snapshot
Theory and Practice of Histotechnology
inferredcites →https://doi.org/10.1155/1980/27685openalex-snapshot
A Kleptoparasitic Cecidomyiid and Other Flies Associated With Spiders
inferredcites →https://doi.org/10.11646/phytotaxa.38.1.6openalex-snapshot
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inferredcites →https://doi.org/10.11646/phytotaxa.46.1.5openalex-snapshot
Phylogenetic relationships in Brazilian Pleurothallis sensu lato (Pleurothallidinae, Orchidaceae): evidence from nuclear ITS rDNA sequences
inferredcites →https://doi.org/10.1177/21.1.73openalex-snapshot
CYTOCHEMICAL REACTIVITY OF POLLEN WALLS
inferredcites →https://doi.org/10.1186/s12862-017-0938-7openalex-snapshot
Exploring the evolutionary origin of floral organs of Erycina pusilla, an emerging orchid model system
inferredcites →https://doi.org/10.1303/aez.9.11openalex-snapshot
Attraction of Several Dipterous Insects to Aliphtic Esters : Diptera : Milichiidae, Chloropidae and Ceratopogonidae
inferredcites →https://doi.org/10.15517/lank.v10i1.18318openalex-snapshot
Lord of the flies: pollination of Dracula orchids
inferredcites →https://doi.org/10.15517/lank.v10i2-3.18317openalex-snapshot
The orchid collections and illustrations of Consul Friedrich C. Lehmann
inferredcites →https://doi.org/10.15517/lank.v11i3.18275openalex-snapshot
Mating systems in the Pleurothallidinae (Orchidaceae): evolutionary and systematic implications
inferredcites →https://doi.org/10.15517/lank.v13i3.14368openalex-snapshot
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inferredcites →https://doi.org/10.15517/lank.v13i3.14429openalex-snapshot
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inferredcites →https://doi.org/10.1590/s0085-56262011005000051openalex-snapshot
Manual of central american diptera
inferredcites →https://doi.org/10.1636/0161-8202-43.3.419openalex-snapshot
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inferredcites →https://doi.org/10.18475/cjos.v46i2.a13openalex-snapshot
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inferredcites →https://doi.org/10.22004/ag.econ.157737openalex-snapshot
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inferredcites →https://doi.org/10.2307/1222385openalex-snapshot
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inferredcites →https://doi.org/10.2307/2389109openalex-snapshot
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inferredcites →https://doi.org/10.2307/3558390openalex-snapshot
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inferredcites →https://doi.org/10.26786/1920-7603(2014)5openalex-snapshot
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inferredcites →https://doi.org/10.2987/09-0005.1openalex-snapshot
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inferredcites →https://doi.org/10.3109/10520297509117023openalex-snapshot
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inferredcites →https://doi.org/10.3389/fevo.2015.00066openalex-snapshot
Deceptive Ceropegia dolichophylla fools its kleptoparasitic fly pollinators with exceptional floral scent
inferredcites →https://doi.org/10.3389/fevo.2015.00141openalex-snapshot
Phytolith Assemblages Along a Gradient of Ancient Human Disturbance in Western Amazonia
inferredcites →https://doi.org/10.3732/ajb.1400012openalex-snapshot
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inferredcites →https://doi.org/10.5281/zenodo.10746072openalex-snapshot
Pollination in the Genus Arum - a review.
inferredcites →https://doi.org/10.5281/zenodo.13190429openalex-snapshot
Forcipomyia hardyi (Diptera: Ceratopogonidae), a Potential Pollinator of Cacao (Theobroma cacao) Flowers in Hawaii
inferredcites →https://doi.org/10.5281/zenodo.15145663openalex-snapshot
Table 1 in A new Gammarus species from Xinjiang Uygur Autonomous Region (China) with a key to Xinjiang freshwater gammarids (Crustacea, Amphipoda, Gammaridae)
inferredcites →https://doi.org/10.5281/zenodo.16001277openalex-snapshot
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inferredcites →https://doi.org/10.5860/choice.48-2671openalex-snapshot
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inferredcites →https://doi.org/10.5962/bhl.part.14427openalex-snapshot
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inferredcites →https://doi.org/10.7751/telopea8127openalex-snapshot
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1111/aen.12629zenodo-depositor-declared
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inferred← citeshttps://doi.org/10.11646/phytotaxa.373.4.4zenodo-depositor-declared
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inferred← citeshttps://doi.org/10.11646/phytotaxa.705.2.1zenodo-depositor-declared
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inferred← citeshttps://doi.org/10.5091/plecevo.164210zenodo-depositor-declared
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inferred← citeshttps://doi.org/10.1002/fedr.201900011openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ppp3.10127openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00606-023-01845-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00606-024-01924-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00709-021-01624-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10886-025-01611-4openalex-snapshot
Cyclopogon guayanensis is an Unusual Orchid with a Generalistic Pollination System and Hexose Dominant Nectar
inferred← citeshttps://doi.org/10.1007/s11829-025-10142-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13355-020-00668-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biocon.2026.111711openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.flora.2022.152179openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jnc.2021.126120openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41598-019-51360-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41598-021-83664-5openalex-snapshot
Plastid phylogenomics resolves ambiguous relationships within the orchid family and provides a solid timeframe for biogeography and macroevolution
inferred← citeshttps://doi.org/10.1038/s41598-022-18031-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1080/23818107.2025.2606196openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/aob/mcaf009openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/botlinnean/boac082openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/botlinnean/boae054openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/botlinnean/boy003openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/774018openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/jse.13119openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/njb.02594openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/nph.17643openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/plb.13113openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/tpj.70883openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s13227-020-00160-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s40529-018-0232-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.15517/lank.v19i3.40082openalex-snapshot
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inferred← citeshttps://doi.org/10.21203/rs.3.rs-1424836/v1openalex-snapshot
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inferred← citeshttps://doi.org/10.32854/agrop.v15i12.2469openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/plants10081564openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/plants9121758openalex-snapshot
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inferred← citeshttps://doi.org/10.3897/neotropical.19.e119499openalex-snapshot
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inferred← citeshttps://doi.org/10.5962/p.340568openalex-snapshot
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