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Thrips pollination of androdioecious Castilla elastica (Moraceae) in a seasonal tropical forest
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/fedr.19961060521openalex-snapshot
Floral biology and pollination of Bocageopsis multiflora and Oxandra euneura in Central Amazonia, with remarks on the evolution of stamens in Annonaceae
inferredcites →https://doi.org/10.1002/j.1537-2197.1964.tb06635.xopenalex-snapshot
THE BREEDING SYSTEM OF OXALIS SUKSDORFII
inferredcites →https://doi.org/10.1002/j.1537-2197.1985.tb05358.xopenalex-snapshot
REPRODUCTIVE BIOLOGY OF TROPICAL LOWLAND RAIN FOREST TREES. II. POLLINATION SYSTEMS
inferredcites →https://doi.org/10.1002/j.1537-2197.1989.tb15086.xopenalex-snapshot
SEX EXPRESSION, BREEDING SYSTEM, AND POLLEN BIOLOGY OF RICINOCARPOS PINIFOLIUS: A CASE OF ANDRODIOECY?
inferredcites →https://doi.org/10.1002/j.1537-2197.1993.tb15291.xopenalex-snapshot
INBREEDING DEPRESSION IN ANDRODIOECIOUS POPULATIONS OF DATISCA GLOMERATA (DATISCACEAE)
inferredcites →https://doi.org/10.1007/bf00940859openalex-snapshot
Pollination of New CaledonianWinteraceae: Opportunistic shifts or parallel radiation with their pollinators?
inferredcites →https://doi.org/10.1007/bf00987602openalex-snapshot
Effect of some floral scents on host finding by thrips (Insecta: Thysanoptera)
inferredcites →https://doi.org/10.1007/bf01508307openalex-snapshot
The maintenance of gynodioecy and androdioecy in angiosperms
inferredcites →https://doi.org/10.1007/bf01975676openalex-snapshot
The fig/pollinator mutualism: A model system for comparative biology
inferredcites →https://doi.org/10.1016/0169-5347(91)90039-zopenalex-snapshot
Cryptic dioecy in flowering plants
inferredcites →https://doi.org/10.1016/s0031-4056(23)00041-0openalex-snapshot
Thrips their biology, ecology and economic importance
inferredcites →https://doi.org/10.1016/s0169-5347(96)10064-1openalex-snapshot
Figs and fig pollinators: evolutionary conflicts in a coevoled mutualism
inferredcites →https://doi.org/10.1038/343641a0openalex-snapshot
Functional androdioecy in the flowering plant Datisca glomerata
inferredcites →https://doi.org/10.1038/359633a0openalex-snapshot
High outcrossing rates maintain male and hermaphrodite individuals in populations of the flowering plant Datisca glomerata
inferredcites →https://doi.org/10.1046/j.1469-8137.1999.00442.xopenalex-snapshot
Androdioecy in the entomophilous tree Fraxinus ornus (Oleaceae)
inferredcites →https://doi.org/10.1073/pnas.89.7.2927openalex-snapshot
Multiple occurrences of mutualism in the yucca moth lineage.
inferredcites →https://doi.org/10.1086/283342openalex-snapshot
A Model for the Evolution of Dioecy and Gynodioecy
inferredcites →https://doi.org/10.1086/285958openalex-snapshot
Evolution of Pollination and Mutualism in the Yucca Moth Lineage
inferredcites →https://doi.org/10.1086/314088openalex-snapshot
Pollen Fertility and Flowering Phenology in an Androdioecious Tree, Fraxinus lanuginosa (Oleaceae), in Hokkaido, Japan
inferredcites →https://doi.org/10.1086/317899openalex-snapshot
Thrips Pollination of the Central Australian Cycad, Macrozamia macdonnellii (Cycadales)
inferredcites →https://doi.org/10.1093/oso/9780198540182.003.0021openalex-snapshot
Thrips of Panama: A biological catalogue and bibliography (Thysanoptera)
inferredcites →https://doi.org/10.1111/j.1095-8312.1984.tb01683.xopenalex-snapshot
Androdioecy and the evolution of dioecy
inferredcites →https://doi.org/10.1111/j.1095-8339.1992.tb00252.xopenalex-snapshot
Is Phillyrea angustifolia L. (Oleaceae) an androdioecious species?
inferredcites →https://doi.org/10.1111/j.1365-2699.1996.tb00014.xopenalex-snapshot
Molecular phylogenies of figs and their pollinator wasps
inferredcites →https://doi.org/10.1111/j.1442-1984.1994.tb00081.xopenalex-snapshot
Pollen Production in the Androdioecious Datisca glomerata (Datiscaceae): Implications for Breeding System Equilibrium
inferredcites →https://doi.org/10.1111/j.1469-7998.1984.tb02364.xopenalex-snapshot
Pollen‐feeding in thrips (Insecta: Thysanoptera)
inferredcites →https://doi.org/10.1111/j.1558-5646.1972.tb00173.xopenalex-snapshot
THE BREAKDOWN OF TRIMORPHIC INCOMPATIBILITY IN OXALIS SECTION CORNICULATAE
inferredcites →https://doi.org/10.1111/j.1744-7429.1998.tb00078.xopenalex-snapshot
Thrips Cross‐Pollination ofPopowia pisocarpa(Annonaceae) in a Lowland Dipterocarp Forest in Sarawak1
inferredcites →https://doi.org/10.1126/science.18.457.436openalex-snapshot
Four New Species of the Central American Rubber Tree
inferredcites →https://doi.org/10.1146/annurev.en.28.010183.002203openalex-snapshot
Insects as Flower Visitors and Pollinators
inferredcites →https://doi.org/10.1146/annurev.es.10.110179.000245openalex-snapshot
Co-Evolution of Figs and Their Insect Pollinators
inferredcites →https://doi.org/10.1890/0012-9658(1997)078[1661:eleoph]2.0.co;2openalex-snapshot
EXAPTATIONS LINK EVOLUTION OF PLANT–HERBIVORE AND PLANT–POLLINATOR INTERACTIONS: A PHYLOGENETIC INQUIRY
inferredcites →https://doi.org/10.2307/1312172openalex-snapshot
Access to the Upper Forest Canopy with a Large Tower Crane
inferredcites →https://doi.org/10.2307/2259462openalex-snapshot
Wind-Pollination in the Understorey of a Rain Forest in Costa Rica
inferredcites →https://doi.org/10.2307/2261072openalex-snapshot
Reproductive System and Population Structure in Three Arctic Saxifraga Species
inferredcites →https://doi.org/10.2307/2387768openalex-snapshot
Patterns of Pollination in the Primitive Angiosperms
inferredcites →https://doi.org/10.2307/2387907openalex-snapshot
Plant Reproductive Ecology of a Secondary Deciduous Tropical Forest in Venezuela
inferredcites →https://doi.org/10.2307/2388806openalex-snapshot
Wind Pollination of Neotropical Dioecious Trees
inferredcites →https://doi.org/10.2307/2388872openalex-snapshot
Ballistic Pollen Release in Australian Members of the Moraceae
inferredcites →https://doi.org/10.2307/2419585openalex-snapshot
Datiscaceae Revisited: Monophyly and the Sequence of Breeding System Evolution
inferredcites →https://doi.org/10.2307/2419835openalex-snapshot
Diversity and Evolutionary Biology of Tropical Flowers.
inferredcites →https://doi.org/10.2307/2446020openalex-snapshot
Pollination biology of two columnar cacti (Neobuxbaumia mezcalaensis and Neobuxbaumia macrocephala) in the Tehuacan Valley, central Mexico
inferredcites →https://doi.org/10.2307/2446435openalex-snapshot
Subandrodioecy and male fitness in Sagittaria lancifolia subsp. lancifolia (Alismataceae)
inferredcites →https://doi.org/10.2307/2484085openalex-snapshot
Pollen Movement and Reproduction in Arisaema triphyllum
inferredcites →https://doi.org/10.2307/2656640openalex-snapshot
Artocarpus (Moraceae)–gall midge pollination mutualism mediated by a male‐flower parasitic fungus
inferredcites →https://doi.org/10.2307/2656708openalex-snapshot
Sex ratios and genetic variation in a functionally androdioecious species, Schizopepon bryoniaefolius (Cucurbitaceae)
inferredcites →https://doi.org/10.2307/2960627openalex-snapshot
Variation in Sex Ratios and Sex Allocation in Androdioecious Mercurialis Annua
inferredcites →https://doi.org/10.2307/2996326openalex-snapshot
Diversity and Evolutionary Biology of Tropical Flowers.
inferredcites →https://doi.org/10.2307/3495826openalex-snapshot
The Thrips of Central and South America: An Introduction (Insecta: Thysanoptera)
inferredcites →https://doi.org/10.3759/tropics.7.165openalex-snapshot
Pollination Biology of the Genus Artocarpus, Moraceae.
inferredcites →https://doi.org/10.5281/zenodo.16386335openalex-snapshot
The Classification of Moraceae
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/phytotaxa.388.4.1zenodo-depositor-declared
Delimitation of the new tribe Parartocarpeae (Moraceae) is supported by a 333-gene phylogeny and resolves tribal level Moraceae taxonomy
inferred← citeshttps://doi.org/10.1590/1806-9665-rbent-2025-0013zenodo-depositor-declared
Population fluctuation and vertical distribution of Thysanoptera in Hancornia speciosa Gomes
inferred← citeshttps://doi.org/10.1002/ece3.7850openalex-snapshot
Floral attraction and flower visitors of a subcanopy, tropical rainforest tree, Fontainea picrosperma
inferred← citeshttps://doi.org/10.1007/978-3-030-66877-8_12openalex-snapshot
Mutualism as a Source of Evolutionary Innovation: Insights from Insect-Plant Interactions
inferred← citeshttps://doi.org/10.1007/s00606-011-0588-yopenalex-snapshot
Functional dioecy in Morinda parvifolia (Rubiaceae), a species with stigma-height dimorphism
inferred← citeshttps://doi.org/10.1007/s00606-018-1548-6openalex-snapshot
Novel reports of laticifers in Moraceae and Urticaceae: revisiting synapomorphies
inferred← citeshttps://doi.org/10.1007/s10265-020-01205-zopenalex-snapshot
Contribution of thrips to seed production in Habenaria radiata, an orchid morphologically adapted to hawkmoths
inferred← citeshttps://doi.org/10.1007/s102650200021openalex-snapshot
A review of brood-site pollination mutualism: plants providing breeding sites for their pollinators
inferred← citeshttps://doi.org/10.1007/s10453-018-9521-yopenalex-snapshot
Pollen diversity in the atmosphere of Havana, Cuba
inferred← citeshttps://doi.org/10.1007/s11427-025-3031-1openalex-snapshot
Floral fragrance in sweet osmanthus majorly repels pollen feeders
inferred← citeshttps://doi.org/10.1007/s11829-016-9443-yopenalex-snapshot
The role of floral structure and biotic factors in determining the occurrence of florivorous thrips in a dystilous shrub
inferred← citeshttps://doi.org/10.1007/s12010-025-05420-zopenalex-snapshot
Geo-Referencing Biochemical Diversity for Conservation Prioritization in Jackfruit (Artocarpus heterophyllus Lam.)
inferred← citeshttps://doi.org/10.1007/s13127-015-0252-4openalex-snapshot
From glacial refugia to wide distribution range: demographic expansion of Loropetalum chinense (Hamamelidaceae) in Chinese subtropical evergreen broadleaved forest
inferred← citeshttps://doi.org/10.1016/j.actao.2018.02.008openalex-snapshot
Morphological diversity and function of the stigma in Ficus species (Moraceae)
inferred← citeshttps://doi.org/10.1016/j.bse.2015.06.009openalex-snapshot
Assessment of genetic diversity among androdioecious ancient Osmanthus fragrans trees by SSR markers
inferred← citeshttps://doi.org/10.1016/j.flora.2016.05.009openalex-snapshot
Morphological traits in an androdioecious species, Chionanthus retusus (Oleaceae)
inferred← citeshttps://doi.org/10.1016/j.flora.2018.01.009openalex-snapshot
Floral development of Moraceae species with emphasis on the perianth and androecium
inferred← citeshttps://doi.org/10.1016/j.revpalbo.2007.12.003openalex-snapshot
Palynological differentiation between genera of the Moraceae family and implications for Amazonian palaeoecology
inferred← citeshttps://doi.org/10.1016/s0169-5347(03)00186-1openalex-snapshot
Not so quiet on the high frontier
inferred← citeshttps://doi.org/10.1017/s0016672307008981openalex-snapshot
Consequences of inbreeding depression due to sex-linked loci for the maintenance of males and outcrossing in branchiopod crustaceans
inferred← citeshttps://doi.org/10.1017/s0266467411000174openalex-snapshot
Pollinators, pollination efficiency and fruiting success in a wild nutmeg, Myristica dactyloides
inferred← citeshttps://doi.org/10.1017/s0266467414000108openalex-snapshot
Effects of forest fragmentation on the recruitment success of the tropical tree Poulsenia armata at Los Tuxtlas, Veracruz, Mexico
inferred← citeshttps://doi.org/10.1017/s096042861200025xopenalex-snapshot
PHYLOGENY, BIOGEOGRAPHY AND CHARACTER EVOLUTION OF DORSTENIA (MORACEAE)
inferred← citeshttps://doi.org/10.1055/s-2003-44784openalex-snapshot
Flower Visitors in a Natural Population of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1073/pnas.0603847103openalex-snapshot
Extensive outcrossing and androdioecy in a vertebrate species that otherwise reproduces as a self-fertilizing hermaphrodite
inferred← citeshttps://doi.org/10.1073/pnas.1120499109openalex-snapshot
Thrips pollination of Mesozoic gymnosperms
inferred← citeshttps://doi.org/10.1079/cabicompendium.11498openalex-snapshot
Castilla elastica (Mexican rubber tree)
inferred← citeshttps://doi.org/10.1080/00222933.2010.534189openalex-snapshot
Ectoparasitism and phoresy in Thysanoptera: the case ofAulacothrips dictyotus(Heterothripidae) in the Neotropical savanna
inferred← citeshttps://doi.org/10.1080/01650521.2012.751785openalex-snapshot
Flower stage and host plant preference by floral herbivore thrips (Insecta: Thysanoptera:Frankliniella) in a Brazilian savanna
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/10.1086/423869openalex-snapshot
Pollination in the New Guinea Endemic Antiaropsis decipiens (Moraceae) Is Mediated by a New Species of Thrips, Thrips antiaropsidis sp. nov. (Thysanoptera: Thripidae)
inferred← citeshttps://doi.org/10.1086/588068openalex-snapshot
The Role of Thrips in Pollination ofArctostaphyllos uva‐ursi
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199642274.003.0026openalex-snapshot
Rapid evolution of pollinator-mediated plant reproductive isolation
inferred← citeshttps://doi.org/10.1093/aesa/saw101openalex-snapshot
Thrips (Thysanoptera) of Coffee Flowers
inferred← citeshttps://doi.org/10.1093/aob/mcaa202openalex-snapshot
What makes a fig: insights from a comparative analysis of inflorescence morphogenesis in Moraceae
inferred← citeshttps://doi.org/10.1093/aob/mcad169openalex-snapshot
Male fertility advantage within and between seasons in the perennial androdioecious plant Phillyrea angustifolia
inferred← citeshttps://doi.org/10.1093/aob/mcaf069openalex-snapshot
Tiny but significant: on the importance of thrips as pollinators
inferred← citeshttps://doi.org/10.1093/aob/mcaf101openalex-snapshot
How to be a big genus? Ficus L. as an emerging model
inferred← citeshttps://doi.org/10.1093/aob/mcn212openalex-snapshot
A new pollination system: brood-site pollination by flower bugs in Macaranga (Euphorbiaceae)
inferred← citeshttps://doi.org/10.1093/aob/mct278openalex-snapshot
Inflorescence dimorphism, heterodichogamy and thrips pollination in Platycarya strobilacea (Juglandaceae)
inferred← citeshttps://doi.org/10.1093/jpe/rtq029openalex-snapshot
Floral resources, pollinators and fruiting in a threatened tropical deciduous tree
inferred← citeshttps://doi.org/10.1111/1442-1984.12183openalex-snapshot
Pollination and reproduction of Psychotria homalosperma , an endangered distylous tree endemic to the oceanic B onin ( O gasawara) I slands, J apan
inferred← citeshttps://doi.org/10.1111/aec.12307openalex-snapshot
On the inability of ants to protect their plant partners and the effect of herbivores on different stages of plant reproduction
inferred← citeshttps://doi.org/10.1111/btp.12144openalex-snapshot
Forest Fragmentation Alters the Population Dynamics of a Late‐successional Tropical Tree
inferred← citeshttps://doi.org/10.1111/btp.12466openalex-snapshot
Combined effects of seed and soil quality drive seedling performance of a late‐successional canopy tree in a tropical forest
inferred← citeshttps://doi.org/10.1111/j.0030-1299.2004.12998.xopenalex-snapshot
Physiological and reproductive differences between hermaphrodites and males in the androdioecious plant Fraxinus ornus
inferred← citeshttps://doi.org/10.1111/j.1365-2028.2011.01302.xopenalex-snapshot
Effects of forest fragmentation on pollination of Mesogyne insignis (Moraceae) in Amani Nature Reserve forests, Tanzania
inferred← citeshttps://doi.org/10.1111/j.1438-8677.2009.00192.xopenalex-snapshot
Pollination ecology and reproductive success in Jack-in-the-pulpit (Arisaema triphyllum) in Québec (Canada)
inferred← citeshttps://doi.org/10.1111/j.1442-1984.2011.00354.xopenalex-snapshot
Breeding system and thrips (Thysanoptera) pollination in the endangered tree Ocotea porosa (Lauraceae): implications for conservation
inferred← citeshttps://doi.org/10.1111/j.1469-185x.2008.00074.xopenalex-snapshot
Consumptive emasculation: the ecological and evolutionary consequences of pollen theft
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2004.01242.xopenalex-snapshot
Repeated evolution of dioecy from androdioecy in Acer
inferred← citeshttps://doi.org/10.1111/jen.13374openalex-snapshot
Unveiling Thrips (Thysanoptera) as Nature's Unsung Pollinators: A Survey From Obligatory Thripophily to Thrips as Supplementary Pollinators
inferred← citeshttps://doi.org/10.1111/nph.70859openalex-snapshot
Brood pollination mutualism between cryptic‐flower Aspidistra and pollen‐parasite midges
inferred← citeshttps://doi.org/10.1111/plb.12119openalex-snapshot
Neither insects nor wind: ambophily in dioecious C hamaedoreapalms ( A recaceae)
inferred← citeshttps://doi.org/10.1111/plb.13616openalex-snapshot
Understanding the relations between Solanaceae crops and their pollinators: a global meta‐network
inferred← citeshttps://doi.org/10.1134/s1234567813090061openalex-snapshot
О ПОЛОВОМ ПОЛИМОРФИЗМЕ НЕКОТОРЫХ АНДРОДИЭЦИЧНЫХ РАСТЕНИЙ, "БОТАНИЧЕСКИЙ ЖУРНАЛ"
inferred← citeshttps://doi.org/10.1139/b02-109openalex-snapshot
Flower mites and nectar production in six hummingbird-pollinated plants with contrasting flower longevities
inferred← citeshttps://doi.org/10.1146/annurev.ecolsys.33.010802.150419openalex-snapshot
The Evolution and Maintenance of Androdioecy
inferred← citeshttps://doi.org/10.1146/annurev.ento.49.061802.123318openalex-snapshot
THYSANOPTERA: Diversity and Interactions
inferred← citeshttps://doi.org/10.11606/d.59.2014.tde-09052014-110717openalex-snapshot
Estruturas secretoras em sicônios de espécies de Ficus L. (Moraceae)
inferred← citeshttps://doi.org/10.1177/194008291300600505openalex-snapshot
Insect Functional Guilds in the Flowering Canopy of Myristica Fatua in a Lowland Swamp, Central Western Ghats, India
inferred← citeshttps://doi.org/10.1186/s12870-021-03319-5openalex-snapshot
A new brood-pollination mutualism between Stellera chamaejasme and flower thrips Frankliniella intonsa
inferred← citeshttps://doi.org/10.1371/journal.pone.0086231openalex-snapshot
Has Pollination Mode Shaped the Evolution of Ficus Pollen?
inferred← citeshttps://doi.org/10.1371/journal.pone.0221898openalex-snapshot
Functional androdioecy in the ornamental shrub Osmanthus delavayi (Oleaceae)
inferred← citeshttps://doi.org/10.15517/rev.biol.trop..v73is2.64541openalex-snapshot
Flowering time and pollinator abundance determine the female reproductive success in the dioecious palm Chamaedorea pinnatifrons (Arecaceae)
inferred← citeshttps://doi.org/10.15560/8.6.1232openalex-snapshot
An updated checklist of the Thysanoptera of Panama with comments on host associations
inferred← citeshttps://doi.org/10.1590/2236-8906-52/2013openalex-snapshot
Atmospheric pollen and spore content in the urban area of the city of Medellin, Colombia
inferred← citeshttps://doi.org/10.1600/036364410x539853openalex-snapshot
Phylogeny and Recircumscription of Artocarpeae (Moraceae) with a Focus on Artocarpus
inferred← citeshttps://doi.org/10.17129/botsci.3081openalex-snapshot
Distribución ecogeográfica y áreas de ocupación de Castilla elastica cerv. en México
inferred← citeshttps://doi.org/10.21829/abm129.2022.1857openalex-snapshot
Germinación, crecimiento inicial y morfología de Castilla elastica (Moraceae) en Tabasco, México
inferred← citeshttps://doi.org/10.21829/azm.2017.3311006openalex-snapshot
Diversidad de tisanópteros en crisantemo [dendranthema grandiflorum]
inferred← citeshttps://doi.org/10.26786/1920-7603(2015)10openalex-snapshot
Minute pollinators: The role of thrips (Thysanoptera) as pollinators of pointleaf manzanita, Arctostaphylos pungens (Ericaceae)
inferred← citeshttps://doi.org/10.3390/d12040141openalex-snapshot
The Influence of Urbanization and Fire Disturbance on Plant-floral Visitor Mutualistic Networks
inferred← citeshttps://doi.org/10.3390/f8090339openalex-snapshot
Traits and Resource Use of Co-Occurring Introduced and Native Trees in a Tropical Novel Forest
inferred← citeshttps://doi.org/10.3398/064.080.0408openalex-snapshot
Breeding System and Pollination of Thermopsis divaricarpa (Fabaceae: Papilionoideae) in the Southern Rocky Mountains
inferred← citeshttps://doi.org/10.3732/ajb.1500279openalex-snapshot
Diversity of fig glands is associated with nursery mutualism in fig trees
inferred← citeshttps://doi.org/10.3732/ajb.89.3.527openalex-snapshot
Aristolochia spp. (Aristolochiaceae) pollinated by flies breeding on decomposing flowers in Panama
inferred← citeshttps://doi.org/10.3732/ajb.91.5.767openalex-snapshot
On the origin of the fig: phylogenetic relationships of Moraceae from ndhF sequences
inferred← citeshttps://doi.org/10.3767/000651905x622815openalex-snapshot
Flora Malesiana precursor for the treatment of Moraceae 8: Other genera than Ficus
inferred← citeshttps://doi.org/10.4038/cmj.v59i3.6568openalex-snapshot
Cardiac toxicity with nodal bradycardia due to Panama rubber (Castilla elastica: Moraceae) poisoning
inferred← citeshttps://doi.org/10.4039/n05-003openalex-snapshot
Thrips (Thysanoptera: Thripidae) on the flowers of a dioecious plant,Dioscorea japonica(Dioscoreaceae)
inferred← citeshttps://doi.org/10.5281/zenodo.7909931openalex-snapshot
Revision of Ceranisus and the related thrips-attacking entedonine genera (Hymenoptera: Eulophidae) of the world
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.23.129openalex-snapshot
Reducing gene flow from pollen dispersal of genetically modified plants in special screened greenhouses
inferred← citeshttps://doi.org/10.6084/m9.figshare.17097868openalex-snapshot
Additional file 1 of A new brood-pollination mutualism between Stellera chamaejasme and flower thrips Frankliniella intonsa
inferred← citeshttps://doi.org/10.6084/m9.figshare.17097871openalex-snapshot
Additional file 2 of A new brood-pollination mutualism between Stellera chamaejasme and flower thrips Frankliniella intonsa
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