On the public citation graph
Thrips Pollination of the Central Australian Cycad, Macrozamia macdonnellii (Cycadales)
0 signed · 102 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1537-2197.1987.tb08582.xopenalex-snapshot
INSECT POLLINATION IN THE CYCAD ZAMIA PUMILA (ZAMIACEAE)
inferredcites →https://doi.org/10.1002/j.1537-2197.1989.tb15117.xopenalex-snapshot
INSECT‐CYCAD SYMBIOSIS AND ITS RELATION TO THE POLLINATION OF ZAMIA FURFURACEA (ZAMIACEAE) BY RHOPALOTRIA MOLLIS (CURCULIONIDAE)
inferredcites →https://doi.org/10.1016/0305-1978(91)90078-eopenalex-snapshot
Cycad cone and angiosperm floral volatiles: Inferences for the evolution of insect pollination
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(99)01811-xopenalex-snapshot
Generalization versus specialization in plant pollination systems
inferredcites →https://doi.org/10.1071/it97014openalex-snapshot
Biology and identification of Aeolothripidae (Thysanoptera) in Australia
inferredcites →https://doi.org/10.1080/002229301447853openalex-snapshot
Thrips (Thysanoptera) pollination in Australian subtropical rainforests, with particular reference to pollination ofWilkiea huegeliana(Monimiaceae)
inferredcites →https://doi.org/10.1080/00222939100770411openalex-snapshot
The first thrips species (Insecta, Thysanoptera) from cycad male cones, and its family level significance
inferredcites →https://doi.org/10.1080/00222939100770611openalex-snapshot
Secondary sexual character variation in maleActinothripsspecies (Insecta: Thysanoptera), and its probable significance in fighting behaviour
inferredcites →https://doi.org/10.1080/00222939700770731openalex-snapshot
A new Brazilian species ofHeterothrips(Insecta: Thysanoptera) co-existing with ants in the flowers ofPeixotoa tomentosa(Malpighiaceae)
inferredcites →https://doi.org/10.1086/317575openalex-snapshot
New Perspectives on the Pollination Biology of Basal Angiosperms
inferredcites →https://doi.org/10.1111/j.1096-3642.1980.tb01934.xopenalex-snapshot
Phylogenetic relationships between the families of recent Thysanoptera (Insecta)
inferredcites →https://doi.org/10.1111/j.1365-2311.1976.tb01203.xopenalex-snapshot
The hosts and distribution of British thrips
inferredcites →https://doi.org/10.1111/j.1469-8137.1953.tb05199.xopenalex-snapshot
THRIPS POLLINATION OF ERICA TETRALIX
inferredcites →https://doi.org/10.2307/2388573openalex-snapshot
The Role of Beetles in the Pollination of Zamia furfuracea L. fil. (Zamiaceae)
inferredcites →https://doi.org/10.2307/2388812openalex-snapshot
Insects Associated with Reproductive Structures of Cycads in Queensland and Northeast New South Wales, Australia
inferredcites →https://doi.org/10.2307/2446138openalex-snapshot
Is there a floral parasite mutualism in cycad pollination? the pollination biology of Encephalartos villosus (Zamiaceae)
inferredcites →https://doi.org/10.5962/bhl.title.104481openalex-snapshot
The effects of cross and self fertilisation in the vegetable kingdom
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112715zenodo-depositor-declared
Unique chemistry associated with diversification in a tightly coupled cycad-thrips obligate pollination mutualism
inferred← citeshttps://doi.org/10.11646/zootaxa.4564.2.1zenodo-depositor-declared
Review of the Aeolothripidae (Thysanoptera) in Japan
inferred← citeshttps://doi.org/10.11646/zootaxa.5150.3.7zenodo-depositor-declared
Two new species of Pharaxonothinae beetles (Coleoptera: Erotylidae) inhabiting cones of the cycad Ceratozamia santillanii Pérez-Farr. & Vovides (Cycadales: Zamiaceae) in Mexico
inferred← citeshttps://doi.org/10.11646/zootaxa.5489.1.6zenodo-depositor-declared
Late Cretaceous thrips (Thysanoptera) from Hti Lin amber
inferred← citeshttps://doi.org/10.1002/9781118945582.ch18openalex-snapshot
Biodiversity of Thysanoptera
inferred← citeshttps://doi.org/10.1007/978-3-030-53226-0_13openalex-snapshot
Collecting and Sampling Methods for Thrips
inferred← citeshttps://doi.org/10.1007/978-94-007-1942-2_9openalex-snapshot
Non Bee Pollinators-Plant Interaction
inferred← citeshttps://doi.org/10.1007/s00114-002-0330-2openalex-snapshot
Cycads: their evolution, toxins, herbivores and insect pollinators
inferred← citeshttps://doi.org/10.1007/s00425-019-03176-5openalex-snapshot
Mechanisms in mutualisms: a chemically mediated thrips pollination strategy in common elder
inferred← citeshttps://doi.org/10.1007/s00442-005-0045-0openalex-snapshot
Experimental evaluation and thermo-physical analysis of thermogenesis in male and female cycad cones
inferred← citeshttps://doi.org/10.1007/s00606-003-0087-xopenalex-snapshot
Association of cone thermogenesis and volatiles with pollinator specificity in Macrozamia cycads
inferred← citeshttps://doi.org/10.1007/s00606-008-0141-9openalex-snapshot
Acer pseudoplatanus (Sapindaceae): Heterodichogamy and thrips pollination
inferred← citeshttps://doi.org/10.1007/s10265-006-0019-2openalex-snapshot
Estragole (4-allylanisole) is the primary compound in volatiles emitted from the male and female cones of Cycas revoluta
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/s11427-025-3031-1openalex-snapshot
Floral fragrance in sweet osmanthus majorly repels pollen feeders
inferred← citeshttps://doi.org/10.1007/s11829-014-9301-8openalex-snapshot
Fire triggers the activity of extrafloral nectaries, but ants fail to protect the plant against herbivores in a neotropical savanna
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/10.1016/j.bse.2003.07.002openalex-snapshot
Genetic differentiation and phenetic relatedness among seven species of the Macrozamia plurinervia complex (Zamiaceae)
inferred← citeshttps://doi.org/10.1016/j.cretres.2016.12.008openalex-snapshot
A new Encephalarteae trunk (Cycadales) from the Cretaceous of Patagonia (Mata Amarilla Formation, Austral Basin), Argentina
inferred← citeshttps://doi.org/10.1016/j.gecco.2026.e04441openalex-snapshot
Genetic diversity, population structure, and dispersal patterns of wild and cultivated Cycas szechuanensis in China
inferred← citeshttps://doi.org/10.1016/j.revpalbo.2008.07.005openalex-snapshot
Morphology and ecology of the Antarcticycas plant
inferred← citeshttps://doi.org/10.1016/j.revpalbo.2021.104487openalex-snapshot
Microsporangiophores from the Early Cretaceous (Berriasian) of Bornholm, Denmark, with comments on a pre-angiosperm xerophytic flora
inferred← citeshttps://doi.org/10.1016/j.ympev.2015.07.003openalex-snapshot
Evolutionary dynamics of a cycad obligate pollination mutualism – Pattern and process in extant Macrozamia cycads and their specialist thrips pollinators
inferred← citeshttps://doi.org/10.1055/s-2003-44784openalex-snapshot
Flower Visitors in a Natural Population of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1071/bt03159openalex-snapshot
Pollination ecology of the Australian cycad Lepidozamia peroffskyana (Zamiaceae)
inferred← citeshttps://doi.org/10.1071/bt06122openalex-snapshot
Environmental determinants of a restricted cycad in central Australia, Macrozamia macdonnellii
inferred← citeshttps://doi.org/10.1071/bt06202openalex-snapshot
Demographics, pollination syndrome and conservation status of Macrozamia platyrhachis (Zamiaceae), a geographically restricted Queensland cycad
inferred← citeshttps://doi.org/10.1073/pnas.1120499109openalex-snapshot
Thrips pollination of Mesozoic gymnosperms
inferred← citeshttps://doi.org/10.1080/00305316.2006.10417487openalex-snapshot
The classification of Terebrantia (Insecta) into families
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/10.1086/321919openalex-snapshot
The Flowers in Extant Basal Angiosperms and Inferences on Ancestral Flowers
inferred← citeshttps://doi.org/10.1086/321929openalex-snapshot
Thrips and Weevils as Dual, Specialist Pollinators of the Australian CycadMacrozamia communis(Zamiaceae)
inferred← citeshttps://doi.org/10.1086/378662openalex-snapshot
Gymnosperms from the Middle Triassic of Antarctica: The First Structurally Preserved Cycad Pollen Cone
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/10.1086/681821openalex-snapshot
Habitats, Trade Winds, and Pollination of the EndangeredCycas micronesica: Is There a Role for Wind as Pollen Vector on the Island of Guam?
inferred← citeshttps://doi.org/10.1086/689200openalex-snapshot
Fine-Scale Genetic Structure ofZamia furfuracea: Variation with Life-Cycle Stages
inferred← citeshttps://doi.org/10.1086/708273openalex-snapshot
Why Are There So Many Flowering Plants? A Multiscale Analysis of Plant Diversification
inferred← citeshttps://doi.org/10.1093/aob/mcac117openalex-snapshot
Phylotranscriptomics reveal the spatio-temporal distribution and morphological evolution ofMacrozamia, an Australian endemic genus of Cycadales
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/mcn212openalex-snapshot
A new pollination system: brood-site pollination by flower bugs in Macaranga (Euphorbiaceae)
inferred← citeshttps://doi.org/10.1093/aob/mct159openalex-snapshot
Patterns of odour emission, thermogenesis and pollinator activity in cones of an African cycad: what mechanisms apply?
inferred← citeshttps://doi.org/10.1098/rstb.2021.0282openalex-snapshot
Colour vision in thrips (Thysanoptera)
inferred← citeshttps://doi.org/10.1111/1365-2435.12239openalex-snapshot
Thrips' responses to thermogenic associated signals in a cycad pollination system: the interplay of temperature, light, humidity and cone volatiles
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/j.1326-6756.2004.00431.xopenalex-snapshot
Australian Thysanoptera – biological diversity and a diversity of studies
inferred← citeshttps://doi.org/10.1111/j.1326-6756.2004.00448.xopenalex-snapshot
Insects ‘Down Under’– Diversity, endemism and evolution of the Australian insect fauna: examples from select orders
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.1472-4642.2012.00936.xopenalex-snapshot
Ancient relicts or recent dispersal: how long have cycads been in central A ustralia?
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/plb.12119openalex-snapshot
Neither insects nor wind: ambophily in dioecious C hamaedoreapalms ( A recaceae)
inferred← citeshttps://doi.org/10.1111/plb.12956openalex-snapshot
Pollination efficiency of cockroaches and other floral visitors of Clusia blattophila
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/10.1126/sciadv.aay6169openalex-snapshot
An ancient push-pull pollination mechanism in cycads
inferred← citeshttps://doi.org/10.1146/annurev.ento.49.061802.123318openalex-snapshot
THYSANOPTERA: Diversity and Interactions
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/10.14393/ufu.te.2014.19openalex-snapshot
Interações multitróficas no cerrado: resultados condicionais nas relações entre plantas, herbívoros e predadores
inferred← citeshttps://doi.org/10.1653/0015-4040(2002)085[0281:adhtfe]2.0.co;2openalex-snapshot
AULACOTHRIPS DICTYOTUS (HETEROTHRIPIDAE), THE FIRST ECTOPARASITIC THRIPS (THYSANOPTERA)
inferred← citeshttps://doi.org/10.1666/0022-3360(2004)078<0941:mtaeeo>2.0.co;2openalex-snapshot
MESOZOIC THRIPS AND EARLY EVOLUTION OF THE ORDER THYSANOPTERA (INSECTA)
inferred← citeshttps://doi.org/10.1666/06026.1openalex-snapshot
Macroecological responses of terrestrial vegetation to climatic and atmospheric change across the Triassic/Jurassic boundary in East Greenland
inferred← citeshttps://doi.org/10.21135/893275150.024openalex-snapshot
An Overview of Cycad Pollination Studies
inferred← citeshttps://doi.org/10.2307/25065852openalex-snapshot
Pollination drops, pollen, and insect pollination of Mesozoic gymnosperms
inferred← citeshttps://doi.org/10.2307/25065853openalex-snapshot
Generalist flowers and phytophagous beetles in two tropical canopy trees: resources for multitudes
inferred← citeshttps://doi.org/10.2307/3558396openalex-snapshot
Thrips pollination of androdioecious Castilla elastica (Moraceae) in a seasonal tropical forest
inferred← citeshttps://doi.org/10.26515/rzsi/v123/i2s/2023/172596openalex-snapshot
An updated checklist of Thrips (Insecta: Thysanoptera) of Sikkim
inferred← citeshttps://doi.org/10.3389/fpls.2018.01844openalex-snapshot
The Evolution of Sexual Fluids in Gymnosperms From Pollination Drops to Nectar
inferred← citeshttps://doi.org/10.3389/fpls.2021.639368openalex-snapshot
Cycad-Weevil Pollination Symbiosis Is Characterized by Rapidly Evolving and Highly Specific Plant-Insect Chemical Communication
inferred← citeshttps://doi.org/10.3390/insects17010103openalex-snapshot
Evolution of Insect Pollination Before Angiosperms and Lessons for Modern Ecosystems
inferred← citeshttps://doi.org/10.3417/2010037openalex-snapshot
The Pollination of Mid Mesozoic Seed Plants and the Early History of Long-proboscid Insects1,2,3
inferred← citeshttps://doi.org/10.3732/ajb.0800016openalex-snapshot
Pollination biology of basal angiosperms (ANITA grade)
inferred← citeshttps://doi.org/10.3732/ajb.89.1.50openalex-snapshot
Thrips pollination of the dioecious ant plant Macaranga hullettii (Euphorbiaceae) in Southeast Asia
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.92.6.931openalex-snapshot
Pollination of Australian Macrozamia cycads (Zamiaceae): effectiveness and behavior of specialist vectors in a dependent mutualism
inferred← citeshttps://doi.org/10.3732/ajb.94.5.847openalex-snapshot
Is Cycas revoluta (Cycadaceae) wind‐ or insect‐pollinated?
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/10.4257/oeco.2009.1301.02openalex-snapshot
ECOLOGIA COMPORTAMENTAL: UMA FERRAMENTA PARA A COMPREENSÃO DAS RELAÇÕES ANIMAIS-PLANTAS
inferred← citeshttps://doi.org/10.5091/plecevo.2015.1142openalex-snapshot
Reproductive morphology in the Gnetum cuspidatum group (Gnetales) and its implications for pollination biology in the Gnetales
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
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.