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Fly pollination in Ceropegia (Apocynaceae: Asclepiadoideae): biogeographic and phylogenetic perspectives

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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/bf00985911openalex-snapshot

Floral biology and pollination in stapeliads ? new results and a literature review

inferredcites →https://doi.org/10.1007/s004420050794openalex-snapshot

Evidence for stabilising selection acting on flowering time in Arum maculatum (Araceae): the influence of phylogeny on adaptation

inferredcites →https://doi.org/10.1007/s10682-008-9259-zopenalex-snapshot

Associations between floral specialization and species diversity: cause, effect, or correlation?

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.sajb.2005.06.005openalex-snapshot

Ceropegia macmasteri (Apocynaceae–Asclepiadoideae–Ceropegieae), a new species from Eastern Cape, South Africa

inferredcites →https://doi.org/10.1016/j.ympev.2006.12.010openalex-snapshot

Biogeographical and phylogenetic origins of African fig species (Ficus section Galoglychia)

inferredcites →https://doi.org/10.1016/j.ympev.2007.09.020openalex-snapshot

Parallel floral adaptations to pollination by fungus gnats within the genus Mitella (Saxifragaceae)

inferredcites →https://doi.org/10.1016/s0169-5347(00)89041-2openalex-snapshot

Diversity and evolutionary biology of tropical flowers

inferredcites →https://doi.org/10.1016/s1055-7903(02)00235-xopenalex-snapshot

Radiation in the Cape flora and the phylogeny of peacock irises Moraea (Iridaceae) based on four plastid DNA regions

inferredcites →https://doi.org/10.1034/j.1600-0706.2002.980215.xopenalex-snapshot

Latitudinal trends in plant‐pollinator interactions: are tropical plants more specialised?

inferredcites →https://doi.org/10.1038/084066a0openalex-snapshot

Handbook of Flower Pollination

inferredcites →https://doi.org/10.1055/s-2001-19367openalex-snapshot

RAPD Analysis and Taxonomic Reconsideration of the Ceropegia aristolochioides Complex (Apocynaceae‐Ceropegieae)

inferredcites →https://doi.org/10.1079/ijt20044openalex-snapshot

Trap-flower fly pollination in East African Ceropegia L. (Apocynaceae)

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/mcg206openalex-snapshot

The Pollination Ecology of an Assemblage of Grassland Asclepiads in South Africa

inferredcites →https://doi.org/10.1098/rspb.2005.3249openalex-snapshot

60 million years of co-divergence in the fig–wasp symbiosis

inferredcites →https://doi.org/10.1111/j.0030-1299.2004.12819.xopenalex-snapshot

A multivariate search for pollination syndromes among penstemons

inferredcites →https://doi.org/10.1111/j.1095-8312.1997.tb00324.xopenalex-snapshot

Pollination systems in the Asclepiadaceae: a survey and preliminary analysis

inferredcites →https://doi.org/10.1111/j.1095-8312.2007.00896.xopenalex-snapshot

Morphological aspects and phylogenetic analyses of pollination systems in the Tylophora-Vincetoxicum complex (Apocynaceae-Asclepiadoideae) in Japan

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.1365-294x.2007.03278.xopenalex-snapshot

Host‐specificity and coevolution among pollinating and nonpollinating New World fig wasps

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.1558-5646.1949.tb00007.xopenalex-snapshot

POLLINATION SYSTEMS AS ISOLATING MECHANISMS IN ANGIOSPERMS

inferredcites →https://doi.org/10.1111/j.1558-5646.1993.tb02170.xopenalex-snapshot

EVOLUTION OF PLANT POLLINATION SYSTEMS: HYPOTHESES AND TESTS WITH THE NEOTROPICAL VINEDALECHAMPIA

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/10.1146/annurev.ecolsys.34.011802.132347openalex-snapshot

Pollination Syndromes and Floral Specialization

inferredcites →https://doi.org/10.1146/annurev.es.01.110170.001515openalex-snapshot

Adaptive Radiation of Reproductive Characteristics in Angiosperms, I: Pollination Mechanisms

inferredcites →https://doi.org/10.1146/annurev.es.25.110194.002231openalex-snapshot

ECOLOGY AND EVOLUTION OF REPRODUCTION IN MILKWEEDS

inferredcites →https://doi.org/10.15468/kwbb45openalex-snapshot

Universal Chalcidoidea Database

inferredcites →https://doi.org/10.1590/s1519-566x2008000300015openalex-snapshot

Primeiro registro de simuliidae (Diptera) com polinários de asclepiadoideae (Apocynaceae)

inferredcites →https://doi.org/10.1600/0363644053661832openalex-snapshot

Phylogenetics of the New World Subtribes of Asclepiadeae (Apocynaceae—Asclepiadoideae): Metastelmatinae, Oxypetalinae, and Gonolobinae

inferredcites →https://doi.org/10.2307/1222585openalex-snapshot

Pollination, adaptation and speciation models in the Cape flora of South Africa

inferredcites →https://doi.org/10.2307/2388572openalex-snapshot

Insect Visitors to Two Forms of Aristolochia pilosa in Las Cumbres, Panama

inferredcites →https://doi.org/10.2307/2419617openalex-snapshot

Phylogenetic and Biogeographical Patterns in Erythrina (Leguminosae: Phaseoleae) as Inferred from Morphological and Chloroplast DNA Characters

inferredcites →https://doi.org/10.2307/2419835openalex-snapshot

Diversity and Evolutionary Biology of Tropical Flowers.

inferredcites →https://doi.org/10.2307/2445883openalex-snapshot

Evolution and homology of bird pollination syndromes in Erythrina (Leguminosae)

inferredcites →https://doi.org/10.2307/25065533openalex-snapshot

Phylogenetics of South American Asclepiadoideae (Apocynaceae)

inferredcites →https://doi.org/10.2307/25065855openalex-snapshot

Multiple meanings and modes: on the many ways to be a generalist flower

inferredcites →https://doi.org/10.2307/25065856openalex-snapshot

The openness of a flower and its number of flower‐visitor species

inferredcites →https://doi.org/10.2307/3546930openalex-snapshot

Pollination, Angiosperm Speciation, and the Nature of Species Boundaries

inferredcites →https://doi.org/10.2307/4135489openalex-snapshot

Subtribal division of Ceropegieae (ApocynaceaeAsclepiadoideae)

inferredcites →https://doi.org/10.3417/0026-6493(2007)94[259:aiatea]2.0.co;2openalex-snapshot

ADVANCES IN APOCYNACEAE: THE ENLIGHTENMENT, AN INTRODUCTION1

inferredcites →https://doi.org/10.3417/0026-6493(2007)94[392:cacspb]2.0.co;2openalex-snapshot

CEROPEGIA (APOCYNACEAE, CEROPEGIEAE, STAPELIINAE): PARAPHYLETIC BUT STILL TAXONOMICALLY SOUND1

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.92.1.13openalex-snapshot

Plant generalization on pollinators: species property or local phenomenon?

inferredcites →https://doi.org/10.4039/ent133439-4openalex-snapshot

Flies and flowers: taxonomic diversity of anthophiles and pollinators

inferredcites →https://doi.org/10.5281/zenodo.10746072openalex-snapshot

Pollination in the Genus Arum - a review.

inferredcites →https://doi.org/10.5281/zenodo.15901442openalex-snapshot

A new species of Leptometopa (Diptera, Milichiidae) from Madagascar pollinating Ceropegia (Asclepiadaceae)

inferredcites →https://doi.org/10.5751/es-00262-050105openalex-snapshot

North American Dipteran Pollinators: Assessing Their Value and Conservation Status

inferredcites →https://doi.org/10.5860/choice.32-3883openalex-snapshot

Diversity and evolutionary biology of tropical flowers

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.5361.2.1zenodo-depositor-declared

A new species of Lygistorrhina (Lygistorrhina) Skuse, 1890 (Diptera: Keroplatidae, Lygistorrhininae) with a key to the subgenus

inferred← citeshttps://doi.org/10.37520/fi.2023.004zenodo-depositor-declared

Diverse fruits and seeds of the mid-Eocene Kishenehn Formation, northwestern Montana, USA, and their implications for biogeography

inferred← citeshttps://doi.org/10.1002/biuz.201770107openalex-snapshot

Leuchterblume täuscht Bestäuber durch Duft verwundeter Bienen

inferred← citeshttps://doi.org/10.1002/ppp3.10261openalex-snapshot

Arisaema: Pollination by lethal attraction

inferred← citeshttps://doi.org/10.1002/ppp3.10494openalex-snapshot

Back from the dead: A fungus gnat pollinator turns Arisaema lethal trap into nursery

inferred← citeshttps://doi.org/10.1002/tax.12827openalex-snapshot

A new concept of Leptadenia (Apocynaceae)

inferred← citeshttps://doi.org/10.1002/tax.70192openalex-snapshot

Diversity of flies visiting and pollinating flowers of the Southern African genus Riocreuxia (Apocynaceae: Ceropegieae, Anisotominae)

inferred← citeshttps://doi.org/10.1002/tax.70251openalex-snapshot

Large‐flowered stapeliad Edithcolea grandis (Apocynaceae: Asclepiadoideae) is pollinated by dung‐ and blood‐feeding African face flies (Muscidae: Musca xanthomelas )

inferred← citeshttps://doi.org/10.1007/s00606-011-0483-6openalex-snapshot

Generalized fly-pollination in Ceropegia ampliata (Apocynaceae–Asclepiadoideae): the role of trapping hairs in pollen export and receipt

inferred← citeshttps://doi.org/10.1007/s00606-012-0725-2openalex-snapshot

A new species of Aspidistra (Ruscaceae s.l., Asparagales) from southern Vietnam, field observations on its flowering and possible pollination by flies (Phoridae)

inferred← citeshttps://doi.org/10.1007/s00606-020-01723-2openalex-snapshot

Molecular phylogenetic analysis and taxonomic reconsideration of Ceropegia hirsuta (Apocynaceae, Asclepiadoideae) reveal a novelty in Thailand, Ceropegia citrina sp. nov., with notes on its pollination ecology

inferred← citeshttps://doi.org/10.1007/s00606-023-01845-3openalex-snapshot

Comparative pollination ecology, fruit and seed set in Corunastylis species (Orchidaceae)

inferred← citeshttps://doi.org/10.1007/s00709-023-01872-4openalex-snapshot

Colleters, osmophores, and nectaries in the species Ceropegia lenewtonii: a sapromyiophilous stapeliad (Asclepiadoideae, Apocynaceae)

inferred← citeshttps://doi.org/10.1007/s11829-013-9270-3openalex-snapshot

Electrophysiological and behavioural responses of the housefly to “sweet” volatiles of the flowers of Caralluma europaea (Guss.) N.E. Br.

inferred← citeshttps://doi.org/10.1016/b978-0-443-33647-8.00007-xopenalex-snapshot

Ceropegia spp.

inferred← citeshttps://doi.org/10.1016/j.cub.2016.07.085openalex-snapshot

Ceropegia sandersonii Mimics Attacked Honeybees to Attract Kleptoparasitic Flies for Pollination

inferred← citeshttps://doi.org/10.1016/j.cub.2025.08.039openalex-snapshot

Squash flowers as microhabitats: the effects of floral temperature and humidity on pollen viability and visitor behavior

inferred← citeshttps://doi.org/10.1016/j.cub.2025.08.060openalex-snapshot

Olfactory floral mimicry of injured ants mediates the attraction of kleptoparasitic fly pollinators

inferred← citeshttps://doi.org/10.1016/j.flora.2016.09.003openalex-snapshot

Entering through the narrow gate: A morphological filter explains specialized pollination of a carrion-scented stapeliad

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1016/j.flora.2017.02.001openalex-snapshot

Floral scent and pollinators of Ceropegia trap flowers

inferred← citeshttps://doi.org/10.1016/j.flora.2017.07.013openalex-snapshot

Diversity of Diptera families that pollinate Ceropegia (Apocynaceae) trap flowers: An update in light of new data and phylogenetic analyses

inferred← citeshttps://doi.org/10.1016/j.flora.2020.151734openalex-snapshot

Pollinators of Hoya pottsii: Are the strongest the most effective?

inferred← citeshttps://doi.org/10.1016/j.phytochem.2011.02.014openalex-snapshot

Pollination by brood-site deception

inferred← citeshttps://doi.org/10.1016/j.ppees.2012.10.002openalex-snapshot

Biological collections in an ever changing world: Herbaria as tools for biogeographical and environmental studies

inferred← citeshttps://doi.org/10.1016/j.sajb.2009.07.017openalex-snapshot

New records of insect pollinators for South African asclepiads (Apocynaceae: Asclepiadoideae)

inferred← citeshttps://doi.org/10.1016/j.sajb.2010.07.022openalex-snapshot

Scent chemistry and pollinator attraction in the deceptive trap flowers of Ceropegia dolichophylla

inferred← citeshttps://doi.org/10.1016/j.sajb.2017.06.021openalex-snapshot

A revised, phylogenetically-based concept of Ceropegia (Apocynaceae)

inferred← citeshttps://doi.org/10.1016/j.ympev.2015.04.015openalex-snapshot

Recent radiation of Brachystelma and Ceropegia (Apocynaceae) across the Old World against a background of climatic change

inferred← citeshttps://doi.org/10.1017/cbo9781139014113.002openalex-snapshot

Macroevolution for plant reproductive biologists

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1071/fp10061openalex-snapshot

Comparative and functional morphology of hierarchically structured anti-adhesive surfaces in carnivorous plants and kettle trap flowers

inferred← citeshttps://doi.org/10.1080/23766808.2018.1542785openalex-snapshot

Determination of apomixis by flow cytometry in two species of Lachemilla (Rosaceae) in Ecuador

inferred← citeshttps://doi.org/10.1086/670367openalex-snapshot

The Importance of Oligosulfides in the Attraction of Fly Pollinators to the Brood-Site Deceptive SpeciesJaborosa rotacea(Solanaceae)

inferred← citeshttps://doi.org/10.1086/697433openalex-snapshot

Functional Morphology and Floral Odor ofDitassa burchellii(Apocynaceae, Asclepiadoideae), a Micromyiophilous Species from Southeastern Brazil

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

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/aob/mcaa072openalex-snapshot

Radiation history of Asian Asarum (sect. Heterotropa, Aristolochiaceae) resolved using a phylogenomic approach based on double-digested RAD-seq data

inferred← citeshttps://doi.org/10.1093/aob/mcaf009openalex-snapshot

A systematic review suggests extension and redefinition of a food-deception pollination syndrome involving anautogenous flies

inferred← citeshttps://doi.org/10.1093/aob/mcp122openalex-snapshot

Ecology and evolution of plant–pollinator interactions

inferred← citeshttps://doi.org/10.1093/aob/mcr268openalex-snapshot

Functional morphology and wasp pollination of two South American asclepiads (Asclepiadoideae–Apocynaceae)

inferred← citeshttps://doi.org/10.1093/aob/mcv119openalex-snapshot

Development and evolution of extreme synorganization in angiosperm flowers and diversity: a comparison of Apocynaceae and Orchidaceae

inferred← citeshttps://doi.org/10.1093/aob/mcy127openalex-snapshot

The diversity and evolution of pollination systems in large plant clades: Apocynaceae as a case study

inferred← citeshttps://doi.org/10.1093/botlinnean/box087openalex-snapshot

Pollination of Trichosalpinx (Orchidaceae: Pleurothallidinae) by biting midges (Diptera: Ceratopogonidae)

inferred← citeshttps://doi.org/10.1093/botlinnean/boz009openalex-snapshot

Pollination by sexual deception of fungus gnats (Keroplatidae and Mycetophilidae) in two clades of Pterostylis (Orchidaceae)

inferred← citeshttps://doi.org/10.1111/1365-2435.12783openalex-snapshot

The specialization continuum in pollination systems: diversity of concepts and implications for ecology, evolution and conservation

inferred← citeshttps://doi.org/10.1111/boj.12054openalex-snapshot

The design of trapping devices in pollination traps of the genusArum(Araceae) is related to insect type

inferred← citeshttps://doi.org/10.1111/eea.70183openalex-snapshot

Unveiling the Diversity of Dipteran Pollinators in the Neotropical Realm

inferred← citeshttps://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)

inferred← citeshttps://doi.org/10.1111/j.1756-1051.2012.01437.xopenalex-snapshot

Reproductive biology and reproductive output assessment in natural and introduced subpopulations of Apium bermejoi, a ‘Critically Endangered’ endemic plant from Menorca (western Mediterranean)

inferred← citeshttps://doi.org/10.1111/jen.13426openalex-snapshot

Pollen Transport Networks Help Reveal the Importance of Dipteran Pollinators in Coastal Plant Communities

inferred← citeshttps://doi.org/10.1111/njb.02594openalex-snapshot

Floral biology and pollination strategy of seven Tacca species (Taccaceae)

inferred← citeshttps://doi.org/10.1111/nph.13210openalex-snapshot

The betrayed thief – the extraordinary strategy of A ristolochia rotunda to deceive its pollinators

inferred← citeshttps://doi.org/10.1111/nph.71562openalex-snapshot

Morphological fit promotes pollen segregation and disassortative pollination in an open‐flowered, nontubular heterostylous species

inferred← citeshttps://doi.org/10.1111/oik.04436openalex-snapshot

Local and regional specialization in plant–pollinator networks

inferred← citeshttps://doi.org/10.1111/plb.13714openalex-snapshot

Fungus gnat pollination in Arisaema urashima: the interplay of lethal traps and mutualistic nurseries

inferred← citeshttps://doi.org/10.1134/s0013873820070015openalex-snapshot

The Fossil Record of Long-Proboscid Nectarivorous Insects

inferred← citeshttps://doi.org/10.1139/cjb-2018-0045openalex-snapshot

Flowering phenology and trap pollination of the rare endemic plant Ceropegia thaithongiae in montane forest of northern Thailand

inferred← citeshttps://doi.org/10.1146/annurev-ecolsys-110316-022919openalex-snapshot

Pollinator Diversity: Distribution, Ecological Function, and Conservation

inferred← citeshttps://doi.org/10.11609/jott.2742.9.11.10865-10879openalex-snapshot

Flies matter: a study of the diversity of Diptera families (Insecta: Diptera) of Mumbai Metropolitan Region, Maharashtra, India, and notes on their ecological roles

inferred← citeshttps://doi.org/10.11646/zootaxa.4048.4.6openalex-snapshot

New World species of Asymphyloptera Collin (Diptera: Empididae: Clinocerinae)

inferred← citeshttps://doi.org/10.17660/actahortic.2020.1267.6openalex-snapshot

Challenge for the sustainable use of Pachypodium genetic resources

inferred← citeshttps://doi.org/10.18596/jotcsa.571770openalex-snapshot

Bioactivity of Phaeophytin a, α-Amyrin and lupeol from Brachystelma togoense Schltr

inferred← citeshttps://doi.org/10.20324/nelumbo/v66/2024/172835openalex-snapshot

A new variety of Ceropegia pubescens (Apocynaceae: Asclepiadoideae) from Neora Valley National Park, Kalimpong, West Bengal.

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.2179/0008-7475.84.1.81openalex-snapshot

Contrasting Pollination Systems of Wild Unction and Devil's Potato Root (Apocynaceae) on San Salvador: Preliminary Observations and Analyses

inferred← citeshttps://doi.org/10.22543/0090-0222.2463openalex-snapshot

Flies associated with floral canopies of the new oilseed crop, pennycress, in the Midwestern U.S.A.

inferred← citeshttps://doi.org/10.26786/1920-7603(2011)1openalex-snapshot

Pollination ecology in the 21st Century: Key questions for future research

inferred← citeshttps://doi.org/10.2985/026.022.0110openalex-snapshot

Three New Species ofBrachystelmafrom Tamil Nadu, India

inferred← citeshttps://doi.org/10.3389/fpls.2017.01119openalex-snapshot

Time-Dependent Trapping of Pollinators Driven by the Alignment of Floral Phenology with Insect Circadian Rhythms

inferred← citeshttps://doi.org/10.3390/plants10081564openalex-snapshot

Fly Pollination of Kettle Trap Flowers of Riocreuxia torulosa (Ceropegieae-Anisotominae): A Generalized System of Floral Deception

inferred← citeshttps://doi.org/10.38061/idunas.570049openalex-snapshot

A Bioactive dihydroflavonol-3-O-α-L-rhamnoside from Bracystelma togoense Schtlr

inferred← citeshttps://doi.org/10.4161/fly.21583openalex-snapshot

The Drosophilidae (Diptera) of the Scattered Islands, with the description of a novel association withLeptadenia madagascariensisDecne. (Apocynaceae)

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