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Mechanistic understanding of perianth traits hindering pollination in Aristolochia contorta Bunge
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/bojl.2000.0438openalex-snapshot
The role of nectar production, flower pigments and odour in the pollination of four species of Passiflora (Passifloraceae) in south-eastern Brazil
inferredcites →https://doi.org/10.1007/978-3-319-96397-6_56openalex-snapshot
Pollinator Trapping in Carnivorous Plants
inferredcites →https://doi.org/10.1007/978-3-319-98482-7openalex-snapshot
A Beginners' Guide to Scanning Electron Microscopy
inferredcites →https://doi.org/10.1007/s004420000531openalex-snapshot
How do visitation patterns vary among pollinators in relation to floral display and floral design in a generalist pollination system?
inferredcites →https://doi.org/10.1007/s004970050138openalex-snapshot
A rapid and simple procedure to determine stigma receptivity
inferredcites →https://doi.org/10.1007/s00606-002-0269-yopenalex-snapshot
Nectar sugar composition in angiosperms from Chaco and Patagonia (Argentina): an animal visitor's matter?
inferredcites →https://doi.org/10.1007/s00709-018-1230-4openalex-snapshot
Pollen ultrastructure in Aristolochia manshuriensis and A. contorta (Aristolochiaceae)
inferredcites →https://doi.org/10.1016/j.ecoleng.2019.05.019openalex-snapshot
Shade and physical support are necessary for conserving the Aristolochia contorta population
inferredcites →https://doi.org/10.1016/j.flora.2005.07.013openalex-snapshot
Floral biology of Aristolochia argentina (Aristolochiaceae)
inferredcites →https://doi.org/10.1016/j.flora.2007.02.006openalex-snapshot
Pollination of Aristolochia pallida Willd. (Aristolochiaceae) in the Mediterranean
inferredcites →https://doi.org/10.1016/j.flora.2013.03.010openalex-snapshot
Embryo structure, seed traits, and productivity of relict vine Aristolochia contorta (Aristolochiaceae)
inferredcites →https://doi.org/10.1016/j.flora.2016.09.005openalex-snapshot
Spatial and temporal variation in volatile composition suggests olfactory division of labor within the trap flowers of Aristolochia gigantea
inferredcites →https://doi.org/10.1016/j.isci.2020.100913openalex-snapshot
Generalist Pollen-Feeding Beetles During the Mid-Cretaceous
inferredcites →https://doi.org/10.1016/j.jep.2009.05.028openalex-snapshot
Local uses of Aristolochia species and content of nephrotoxic aristolochic acid 1 and 2—A global assessment based on bibliographic sources
inferredcites →https://doi.org/10.1016/j.phytochem.2011.03.013openalex-snapshot
The effects of herbivore-induced plant volatiles on interactions between plants and flower-visiting insects
inferredcites →https://doi.org/10.1016/j.plantsci.2012.07.007openalex-snapshot
Histochemical location of key enzyme activities involved in receptivity and self-incompatibility in the olive tree (Olea europaea L.)
inferredcites →https://doi.org/10.1016/j.sajb.2010.07.012openalex-snapshot
Convergent evolution of carrion and faecal scent mimicry in fly-pollinated angiosperm flowers and a stinkhorn fungus
inferredcites →https://doi.org/10.1016/j.scienta.2005.02.007openalex-snapshot
Effect of temperature on seed and fruit development in three mango (Mangifera indica L.) cultivars
inferredcites →https://doi.org/10.1016/j.scitotenv.2020.143507openalex-snapshot
Reduced host plant growth and increased tyrosine-derived secondary metabolites under climate change and negative consequences on its specialist herbivore
inferredcites →https://doi.org/10.1016/j.scitotenv.2022.156065openalex-snapshot
Ontogeny-dependent effects of elevated CO2 and watering frequency on interaction between Aristolochia contorta and its herbivores
inferredcites →https://doi.org/10.1016/s0367-2530(17)30812-5openalex-snapshot
Remarkable nectaries: structure, ecology, organophyletic perspectives
inferredcites →https://doi.org/10.1016/s0378-8741(98)00123-8openalex-snapshot
Quantitative analysis of aristolochic acids, toxic compounds, contained in some medicinal plants
inferredcites →https://doi.org/10.1038/s41598-022-18031-zopenalex-snapshot
Pollinator and floral odor specificity among four synchronopatric species of Ceropegia (Apocynaceae) suggests ethological isolation that prevents reproductive interference
inferredcites →https://doi.org/10.1046/j.1570-7458.2002.01028.xopenalex-snapshot
Attachment ability of the beetle Chrysolina fastuosa on various plant surfaces
inferredcites →https://doi.org/10.1079/ijt20044openalex-snapshot
Trap-flower fly pollination in East African Ceropegia L. (Apocynaceae)
inferredcites →https://doi.org/10.1080/0028825x.2017.1380051openalex-snapshot
Floral anatomy, micromorphology and visitor insects in three species of Aristolochia L. (Aristolochiaceae)
inferredcites →https://doi.org/10.1080/15563650600671712openalex-snapshot
Aristolochic Acids Detected in Some Raw Chinese Medicinal Herbs and Manufactured Herbal Products – A Consequence of Inappropriate Nomenclature and Imprecise Labelling?
inferredcites →https://doi.org/10.1080/17550874.2013.770934openalex-snapshot
Pollination biology and floral longevity ofAristolochia chilensisin an arid ecosystem
inferredcites →https://doi.org/10.1086/593047openalex-snapshot
Pollination Biology of Hydnora africana Thunb. (Hydnoraceae) in Namibia: Brood‐Site Mimicry with Insect Imprisonment
inferredcites →https://doi.org/10.1093/aesa/86.5.609openalex-snapshot
Pollination of Aristolochia littoralis (Aristolochiales: Aristolochiaceae) by Males of Megaselia spp. (Diptera: Phoridae)
inferredcites →https://doi.org/10.1093/aob/mcf021openalex-snapshot
The Pollination Mechanism in Trigonidium obtusum Lindl (Orchidaceae: Maxillariinae): Sexual Mimicry and Trap-flowers
inferredcites →https://doi.org/10.1093/aob/mcn152openalex-snapshot
Pollination Biology of Jacaranda oxyphylla with an Emphasis on Staminode Function
inferredcites →https://doi.org/10.1111/1365-2664.12257openalex-snapshot
Flower plantings increase wild bee abundance and the pollination services provided to a pollination‐dependent crop
inferredcites →https://doi.org/10.1111/j.1095-8312.2007.00796.xopenalex-snapshot
Noncorrelated evolution between herbivore- and pollinator-linked features in Aristolochia chilensis (Aristolochiaceae)
inferredcites →https://doi.org/10.1111/j.1095-8339.2000.tb01537.xopenalex-snapshot
A survey of the function of the lethal kettle traps of Arisaema (Araceae), with records of pollinating fungus gnats from Nepal
inferredcites →https://doi.org/10.1111/j.1438-8677.2008.00131.xopenalex-snapshot
Pollinators, flowering phenology and floral longevity in two Mediterranean Aristolochia species, with a review of flower visitor records for the genus
inferredcites →https://doi.org/10.1111/j.1438-8677.2010.00396.xopenalex-snapshot
Persistently low fruiting success in the Mediterranean pipevine Aristolochia baetica (Aristolochiaceae): a multi‐year study
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.03013.xopenalex-snapshot
Structure and biomechanics of trapping flower trichomes and their role in the pollination biology ofAristolochiaplants (Aristolochiaceae)
inferredcites →https://doi.org/10.1111/jbi.12198openalex-snapshot
Present trans‐Pacific disjunct distribution of A ristolochia subgenus I sotrema ( A ristolochiaceae) was shaped by dispersal, vicariance and extinction
inferredcites →https://doi.org/10.1111/nph.13328openalex-snapshot
Trickery flowers: the extraordinary chemical mimicry of Aristolochia to accomplish deception to its pollinators
inferredcites →https://doi.org/10.1111/plb.12503openalex-snapshot
Spatio‐temporal patterns in pollination of deceptiveAristolochia rotundaL. (Aristolochiaceae)
inferredcites →https://doi.org/10.1111/plb.13497openalex-snapshot
Pollination biology of Aristolochia bianorii Sennen & Pau: promoting cross‐pollination but assuring reproductive success in island ecosystems
inferredcites →https://doi.org/10.1127/1869-6155/2014/0131-0075openalex-snapshot
Nectar secretion and nectaries in basal angiosperms, magnoliids and non-core eudicots and a comparison with core eudicots
inferredcites →https://doi.org/10.1134/s1022795411120088openalex-snapshot
Genetic diversity of a rare species Aristolochia contorta Bunge (Aristolochiaceae) in Primorsky Krai
inferredcites →https://doi.org/10.1139/b2012-047openalex-snapshot
Pollination biology and genetic variability of a giant perfumed flower (Aristolochia giganteaMart. and Zucc., Aristolochiaceae) visited mainly by small Diptera
inferredcites →https://doi.org/10.1146/annurev.ecolsys.36.102403.115320openalex-snapshot
Pollen Limitation of Plant Reproduction: Pattern and Process
inferredcites →https://doi.org/10.1146/annurev.en.28.010183.002203openalex-snapshot
Insects as Flower Visitors and Pollinators
inferredcites →https://doi.org/10.1155/2019/8125063openalex-snapshot
Optimizing Irrigation Water and N Levels for Higher Yield and Reduced Blossom End Rot Incidence on Tomato
inferredcites →https://doi.org/10.1201/9781420004007.sec4openalex-snapshot
Relationship between Floral Fragrance Composition and Type of Pollinator
inferredcites →https://doi.org/10.14411/eje.2001.057openalex-snapshot
Scuttle flies (Diptera: Phoridae) whose larvae develop in flowers of Aristolochia (Aristolochiaceae) in Panama
inferredcites →https://doi.org/10.1590/s1676-06032013000100043openalex-snapshot
Thrips species (Insecta: Thysanoptera) associated to Cowpea in Piauí, Brazil
inferredcites →https://doi.org/10.17663/jwr.2020.22.2.100openalex-snapshot
An analysis of the genetic diversity of a riparian marginal species, Aristolochia contorta
inferredcites →https://doi.org/10.1890/0012-9658(2000)081[0015:ftscod]2.0.co;2openalex-snapshot
FLOWER-TO-SEEDLING CONSEQUENCES OF DIFFERENT POLLINATION REGIMES IN AN INSECT-POLLINATED SHRUB
inferredcites →https://doi.org/10.1890/03-8024openalex-snapshot
POLLEN LIMITATION OF PLANT REPRODUCTION: ECOLOGICAL AND EVOLUTIONARY CAUSES AND CONSEQUENCES
inferredcites →https://doi.org/10.1890/11-0967.1openalex-snapshot
Pollinator effectiveness varies with experimental shifts in flowering time
inferredcites →https://doi.org/10.21203/rs.3.rs-1424836/v1openalex-snapshot
Pollinator and Floral Odor Specificity Among Four Synchronopatric Species of Ceropegia (Apocynaceae) Suggests Ethological Isolation That Prevents Reproductive Interference
inferredcites →https://doi.org/10.2307/1222385openalex-snapshot
The Role of Scent Glands in Pollination: On the Structure and Function of Osmophores
inferredcites →https://doi.org/10.2307/1308218openalex-snapshot
Why Are There So Many Kinds of Flowering Plants?
inferredcites →https://doi.org/10.2307/2388572openalex-snapshot
Insect Visitors to Two Forms of Aristolochia pilosa in Las Cumbres, Panama
inferredcites →https://doi.org/10.2307/2394940openalex-snapshot
Revision of the North and Central American Hexandrous Species of Aristolochia (Aristolochiaceae)
inferredcites →https://doi.org/10.26786/1920-7603(2012)15openalex-snapshot
Pollen analyses for pollination research, unacetolyzed pollen
inferredcites →https://doi.org/10.3389/fevo.2021.658441openalex-snapshot
Flowers of Deceptive Aristolochia microstoma Are Pollinated by Phorid Flies and Emit Volatiles Known From Invertebrate Carrion
inferredcites →https://doi.org/10.3389/finsc.2023.1145761openalex-snapshot
Ants are more than just curious bystanders to some flowers—they act as significant pollinators
inferredcites →https://doi.org/10.3732/ajb.89.3.527openalex-snapshot
Aristolochia spp. (Aristolochiaceae) pollinated by flies breeding on decomposing flowers in Panama
inferredcites →https://doi.org/10.3732/ajb.92.7.1114openalex-snapshot
Pollen movement in a natural population of Arisaema serratum (Araceae), a plant with a pitfall‐trap flower pollination system
inferredcites →https://doi.org/10.3732/ajb.93.4.599openalex-snapshot
A multi‐year study of factors affecting fruit production in Aristolochia paucinervis (Aristolochiaceae)
inferredcites →https://doi.org/10.5091/plecevo.2021.1747openalex-snapshot
Poor fruit set due to lack of pollinators in Aristolochia manshuriensis (Aristolochiaceae)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.5091/plecevo.163430zenodo-depositor-declared
Does size matter? Pollination biology of Aristolochia sessilifolia (Aristolochiaceae)
inferred← citeshttps://doi.org/10.1002/ece3.71175openalex-snapshot
Ecological Dynamics of Volatile Organic Compound–Mediated Interactions in Aristolochia Contorta With Parasitoids and Herbivores
inferred← citeshttps://doi.org/10.1016/j.aspen.2026.102565openalex-snapshot
Two newly reported pollinator species of Dasyhelea (Diptera: Ceratopogonidae) from flowers of Aristolochia contorta Bunge in Korea
inferred← citeshttps://doi.org/10.1016/j.indic.2026.101399openalex-snapshot
Development of a trait-based resilience indicator: a case study of Aristolochia contorta under drought and elevated CO2 conditions
inferred← citeshttps://doi.org/10.1101/2025.05.29.656634openalex-snapshot
Phylogenomics of Aristolochia subg. Siphisi a (Aristolochiaceae) reveals widespread incomplete lineage sorting and supports a novel pollinator-filtering hypothesis
inferred← citeshttps://doi.org/10.1111/1365-2435.14633openalex-snapshot
Sex, flies and flower trap: Trapping trichomes and their function in pollination
inferred← citeshttps://doi.org/10.1111/1365-2435.70024openalex-snapshot
Intraspecific seed competition and genetic diversity within the capsule fruits of Aristolochia contorta
inferred← citeshttps://doi.org/10.3389/fpls.2024.1359783openalex-snapshot
The reduced growth due to elevated CO2 concentration hinders the sexual reproduction of mature Northern pipevine (Aristolochia contorta Bunge)
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