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The Role of Thrips in Pollination ofArctostaphyllos uva‐ursi
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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/j.1537-2197.1991.tb14499.xopenalex-snapshot
THRIPS‐MEDIATED SELF‐POLLINATION OF TWO FACULTATIVELY XENOGAMOUS WETLAND SPECIES
inferredcites →https://doi.org/10.1006/anbo.1998.0845openalex-snapshot
Pollination Ecology ofChloranthus serratus(Thunb.) Roem. et Schult. andCh. fortunei(A. Gray) Solms-Laub. (Chloranthaceae)
inferredcites →https://doi.org/10.1007/978-0-387-21706-2openalex-snapshot
Modern Applied Statistics with S
inferredcites →https://doi.org/10.1007/s00606-004-0236-xopenalex-snapshot
Floral features and reproductive ecology in Thymelaea hirsuta (L.) Endl.
inferredcites →https://doi.org/10.1016/j.flora.2005.07.011openalex-snapshot
An ancient pollinator of a contemporary plant (Cyclamen persicum): When pollination syndromes break down
inferredcites →https://doi.org/10.1080/00173130310016211openalex-snapshot
Pollen harvest by solitary bees ( Ptilothrix relata , Hym. Apidae, Emphorini) in the Argentine pampas – preliminary results
inferredcites →https://doi.org/10.1080/00173134.2004.11877463openalex-snapshot
Pollination, pollen germination and stigma receptivity inMoringa oleiferaLamk
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/10.1080/10618600.1996.10474713openalex-snapshot
R: A Language for Data Analysis and Graphics
inferredcites →https://doi.org/10.1086/317899openalex-snapshot
Thrips Pollination of the Central Australian Cycad, Macrozamia macdonnellii (Cycadales)
inferredcites →https://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)
inferredcites →https://doi.org/10.1111/j.1365-2311.1985.tb00725.xopenalex-snapshot
Pollen‐feeding and the host specificity and fecundity of flower thrips (Thysanoptera)
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.1469-8137.1953.tb05199.xopenalex-snapshot
THRIPS POLLINATION OF ERICA TETRALIX
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/10.1111/j.1744-7429.2001.tb00199.xopenalex-snapshot
Morphology and Biology of Napoleonaea vogelii (Lecythidaceae) Flowers in Relation to the Natural History of Insect Visitors1
inferredcites →https://doi.org/10.1139/b98-133openalex-snapshot
The generalist pollination system and reproductive success of Calluna vulgaris in the Upper Ardenne
inferredcites →https://doi.org/10.1890/0012-9658(1999)080[0786:cooitp]2.0.co;2openalex-snapshot
CONDITIONAL OUTCOMES OF INTERACTIONS: THE POLLINATOR–PREY CONFLICT OF AN INSECTIVOROUS PLANT
inferredcites →https://doi.org/10.2307/3558396openalex-snapshot
Thrips pollination of androdioecious Castilla elastica (Moraceae) in a seasonal tropical forest
inferredcites →https://doi.org/10.3732/ajb.89.1.50openalex-snapshot
Thrips pollination of the dioecious ant plant Macaranga hullettii (Euphorbiaceae) in Southeast Asia
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.4750.3.13zenodo-depositor-declared
A new species of the genus Thrips (Thysanoptera, Thripidae) from the Malagasy Region
inferred← citeshttps://doi.org/10.11646/zootaxa.5884.1.11zenodo-depositor-declared
A new species of Thrips Linnaeus (Thripidae, Thripinae) from the cold deserts of Ladakh, India
inferred← citeshttps://doi.org/10.3897/zookeys.1192.117754zenodo-depositor-declared
New stenurothripid thrips from mid-Cretaceous Kachin amber (Thysanoptera, Stenurothripidae)
inferred← citeshttps://doi.org/10.1002/ajb2.16220openalex-snapshot
The evolution of Ericaceae flowers and their pollination syndromes at a global scale
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/s10841-016-9945-zopenalex-snapshot
Patterns of diversity of flower-visitor assemblages to the understory Araceae in a tropical mountain forest in Colombia
inferred← citeshttps://doi.org/10.1007/s11829-015-9399-3openalex-snapshot
Florivory and nectar-robbing perforations in flowers of pointleaf manzanita Arctostaphylos pungens (Ericaceae) and their effects on plant reproductive success
inferred← citeshttps://doi.org/10.1007/s40011-014-0307-xopenalex-snapshot
Reproductive Assurance Through Autogamy in Some Annual Weed Species
inferred← citeshttps://doi.org/10.1016/j.pbi.2011.03.023openalex-snapshot
Back to the past for pollination biology
inferred← citeshttps://doi.org/10.1093/aob/mcae164openalex-snapshot
Elevational shifts in reproductive ecology indicate the climate response of a model chasmophyte, Rainer’s bellflower (Campanula raineri)
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/jipm/pmae016openalex-snapshot
Pollen-borne ilarviruses of peach: biology, ecology, and disease management
inferred← citeshttps://doi.org/10.1093/jxb/erm028openalex-snapshot
Flowering Newsletter bibliography for 2006
inferred← citeshttps://doi.org/10.1093/jxb/erp154openalex-snapshot
Flowering Newsletter bibliography for 2008
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/10.2478/oszn-2013-0025openalex-snapshot
Thrips (Thysanoptera, Insecta) of the Asteraceae family plants occurring in areas with different levels of anthropopressure in Lublin (Eastern Poland) / Wciornastki (Thysanoptera, Insecta) zebrane z miejsc o różnym stopniu antropopresji w Lublinie na roślinach z rodziny Asteraceae
inferred← citeshttps://doi.org/10.2478/v10014-009-0016-yopenalex-snapshot
Distribution of Thysanoptera species and their host plants in Croatia
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/d15040514openalex-snapshot
The Terebrantia (Insecta: Thysanoptera) of the Maltese Islands
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/10.3897/zookeys.1180.107065openalex-snapshot
The Tubulifera (Hexapoda, Thysanoptera) of the Maltese Islands
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