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Nectar, Floral Morphology and Pollination Syndrome in Loasaceae subfam. Loasoideae (Cornales)
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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.1537-2197.1981.tb06373.xopenalex-snapshot
FLORAL STRUCTURE AND MECHANISM IN LOASACEAE
inferredcites →https://doi.org/10.1002/j.1537-2197.1981.tb12389.xopenalex-snapshot
FUNCTION OF MENTZELIA NUDA (LOASACEAE) POSTFLORAL NECTARIES IN SEED DEFENSE
inferredcites →https://doi.org/10.1002/j.1537-2197.1982.tb13237.xopenalex-snapshot
COMMUNITY STUDIES IN POLLINATION ECOLOGY IN THE HIGH TEMPERATE ANDES OF CENTRAL CHILE. I. POLLINATION MECHANISMS AND ALTITUDINAL VARIATION
inferredcites →https://doi.org/10.1002/j.1537-2197.1988.tb08802.xopenalex-snapshot
FLORAL NECTAR SUGAR COMPOSITION AND POLLINATOR TYPE AMONG NEW WORLD GENERA IN TRIBE ANTIRRHINEAE (SCROPHULARIACEAE)
inferredcites →https://doi.org/10.1006/anbo.2000.1331openalex-snapshot
Nectar Sugar Composition in Relation to Pollination Syndromes in Sinningieae (Gesneriaceae)
inferredcites →https://doi.org/10.1007/bf00377434openalex-snapshot
On the calculation of sugar concentration in flower nectar
inferredcites →https://doi.org/10.1007/bf00379522openalex-snapshot
Optimal sugar concentrations of floral nectars ?dependence on sugar intake efficiency and foraging costs
inferredcites →https://doi.org/10.1007/bf00388069openalex-snapshot
Nectar production of Epilobium angustifolium L. at different air humidities; nectar sugar in individual flowers and the optimal foraging theory
inferredcites →https://doi.org/10.1007/bf00696435openalex-snapshot
Energetics of nectar extraction in a small, high altitude, tropical hummingbird,Selasphorus flammula
inferredcites →https://doi.org/10.1007/bf00984916openalex-snapshot
Evidence of rodent pollination inCajophora coronata (Loasaceae)
inferredcites →https://doi.org/10.1007/bf00985047openalex-snapshot
Phylogeny of the tribe Antirrhineae (Scrophulariaceae) based on morphological andndhF sequence data
inferredcites →https://doi.org/10.1007/s00606-002-0277-yopenalex-snapshot
Nectar biodiversity: a short review
inferredcites →https://doi.org/10.1016/j.ode.2003.12.001openalex-snapshot
A preliminary phylogeny of Loasaceae subfam. Loasoideae (Angiospermae: Cornales) based on L sequence data, with consequences for systematics and historical biogeography
inferredcites →https://doi.org/10.1016/s0305-1978(97)00030-6openalex-snapshot
Floral nectar chemical composition of some species from Patagonia
inferredcites →https://doi.org/10.1016/s0367-2530(17)30851-4openalex-snapshot
The relationship between floral nectar composition and visitors in Lycium (Solanaceae) from Argentina and Chile: what does it reflect?
inferredcites →https://doi.org/10.1043/02-38.1openalex-snapshot
A Revision of Nasa ser. Carunculatae (Loasaceae subfam. Loasoideae)
inferredcites →https://doi.org/10.1055/s-2005-873034openalex-snapshot
Evolution of Funnel-Revolver Flowers and Ornithophily in Nasa (Loasaceae)
inferredcites →https://doi.org/10.1080/15230430.2002.12003490openalex-snapshot
Plant-Pollinator Relationships at Two Altitudes in the Andes of Mendoza, Argentina
inferredcites →https://doi.org/10.1086/427477openalex-snapshot
A Phylogenetic Analysis of Loasaceae Subfamily Loasoideae Based on Plastid DNA Sequences
inferredcites →https://doi.org/10.1093/aob/mcj043openalex-snapshot
Nectar Concentration and Composition of 26 Species from the Temperate Forest of South America
inferredcites →https://doi.org/10.1093/oso/9780195063943.003.0008openalex-snapshot
Nectar Production, Flowering Phenology, and Strategies for Pollination
inferredcites →https://doi.org/10.1111/j.0014-3820.2002.tb00139.xopenalex-snapshot
MINOR QUANTITATIVE TRAIT LOCI UNDERLIE FLORAL TRAITS ASSOCIATED WITH MATING SYSTEM DIVERGENCE IN MIMULUS
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb00347.xopenalex-snapshot
AFLP PHYLOGENY OF MIMULUS SECTION ERYTHRANTHE AND THE EVOLUTION OF HUMMINGBIRD POLLINATION
inferredcites →https://doi.org/10.1111/j.1365-2311.1979.tb00557.xopenalex-snapshot
Humidity, nectar and insect visits to flowers, with special reference to Crataegus, Tilia and Echium
inferredcites →https://doi.org/10.1111/j.1365-3040.1979.tb00084.xopenalex-snapshot
Post‐secretory determinants of sugar concentration in nectar
inferredcites →https://doi.org/10.1111/j.1438-8677.1892.tb04450.xopenalex-snapshot
37. Ign. Urban: Blüthen‐ und Fruchtbau der Loasaceen
inferredcites →https://doi.org/10.1111/j.1438-8677.1997.tb00626.xopenalex-snapshot
Micro‐Foraging Routes of Bicolletes pampeana (Colletidae) and Bee‐Induced Pollen Presentation in Cajophora arechavaletae (Loasaceae)
inferredcites →https://doi.org/10.1111/j.1744-7429.2004.tb00312.xopenalex-snapshot
Nectar in Hummingbird‐pollinated Neotropical Plants I: Patterns of Production and Variability in 12 Species
inferredcites →https://doi.org/10.1111/j.1756-1051.2000.tb00727.xopenalex-snapshot
A revision of the Peruvian species of Nasa ser. Alatae (Loasaceae)
inferredcites →https://doi.org/10.1126/science.176.4035.597openalex-snapshot
Energetics and Pollination Ecology
inferredcites →https://doi.org/10.1127/0006-8152/2003/0124-0345openalex-snapshot
A revision of the Nasa stuebeliana group Nasa Weigend ser. Saccatae (Urb. & Gilg) Weigend p.p., Loasaceae with notes on morphology, ecology, and distribution
inferredcites →https://doi.org/10.1139/b00-055openalex-snapshot
Floral nectary structure and nectar chemical composition of some species from Robinson Crusoe Island (Chile)
inferredcites →https://doi.org/10.1139/b81-025openalex-snapshot
Nectar production in the boreal forest lily Clintonia borealis
inferredcites →https://doi.org/10.15381/rpb.v11i2.2447openalex-snapshot
Observaciones adicionales sobre la biogeografía de la zona de Amotape-Huancabamba en el norte del Perú
inferredcites →https://doi.org/10.1650/0010-5422(2000)102[0235:rhsppo]2.0.co;2openalex-snapshot
RUFOUS HUMMINGBIRD SUCROSE PREFERENCE: PRECISION OF SELECTION VARIES WITH CONCENTRATION
inferredcites →https://doi.org/10.1663/0006-8101(2002)068[0038:ootbot]2.0.co;2openalex-snapshot
Observations on the Biogeography of the Amotape-Huancabamba Zone in Northern Peru
inferredcites →https://doi.org/10.2307/1370432openalex-snapshot
Rufous Hummingbird Sucrose Preference: Precision of Selection Varies with Concentration
inferredcites →https://doi.org/10.2307/2387684openalex-snapshot
Why Do Hummingbird Flowers Secrete Dilute Nectar?
inferredcites →https://doi.org/10.2307/2387804openalex-snapshot
The Production of Dilute Nectars by Hummingbird and Honeyeater Flowers
inferredcites →https://doi.org/10.2307/2389183openalex-snapshot
Patterns in Floral Nectar Characteristics of Some Bird-Visited Plant Species From Costa Rica
inferredcites →https://doi.org/10.2307/2657108openalex-snapshot
Drought stress, plant water status, and floral trait expression in fireweed, Epilobium angustifolium (Onagraceae)
inferredcites →https://doi.org/10.2307/2989798openalex-snapshot
Sugar Concentrations in Nectars from Hummingbird Flowers
inferredcites →https://doi.org/10.2307/3544346openalex-snapshot
Plant Reproduction and Optimal Foraging: Experimental Nectar Manipulations in Delphinium Nelsonii
inferredcites →https://doi.org/10.3732/ajb.90.3.445openalex-snapshot
Systematics and evolution of tribe Sinningieae (Gesneriaceae): evidence from phylogenetic analyses of six plastid DNA regions and nuclear ncpGS
inferredcites →https://doi.org/10.3732/ajb.90.8.1215openalex-snapshot
The major clades of Loasaceae: phylogenetic analysis using the plastid matK and trnL‐trnF regions
inferredcites →https://doi.org/10.3732/ajb.92.8.1270openalex-snapshot
Nectar traits in Nicotiana section Alatae (Solanaceae) in relation to floral traits, pollinators, and mating system
inferredcites →https://doi.org/10.4067/s0717-73562003000100005openalex-snapshot
ETNOBOTÁNICA DEL SUR DE LOS ANDES DE LA PRIMERA REGIÓN DE CHILE: UN ENLACE ENTRE LAS CULTURAS ALTIPLÁNICAS Y LAS DE QUEBRADAS ALTAS DEL LOA SUPERIOR
inferredcites →https://doi.org/10.5281/zenodo.16010618openalex-snapshot
Four new species of Nasa ser. Alatae (Loasaceae) in the Amotape-Huancabamba Zone of Peru
inferredcites →https://doi.org/10.5860/choice.32-3883openalex-snapshot
Diversity and evolutionary biology of tropical flowers
inferredcites →https://doi.org/10.5962/p.67866openalex-snapshot
Floral biology and systematics of Eucnide (Loasaceae)
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.236.2.9zenodo-depositor-declared
A new, narrowly endemic species of Blumenbachia (Loasaceae subfam. Loasoideae) from Brazil
inferred← citeshttps://doi.org/10.1002/tax.603004openalex-snapshot
Phylogenetic relationships and morphological diversity in Neotropical Heliotropium (Heliotropiaceae)
inferred← citeshttps://doi.org/10.1007/978-1-4020-9609-9_2openalex-snapshot
Class Magnoliopsida (Dicotyledons)
inferred← citeshttps://doi.org/10.1007/s10682-016-9826-7openalex-snapshot
Flower reshaping in the transition to hummingbird pollination in Loasaceae subfam. Loasoideae despite absence of corolla tubes or spurs
inferred← citeshttps://doi.org/10.1007/s10682-017-9887-2openalex-snapshot
Pollinator type and secondarily climate are related to nectar sugar composition across the angiosperms
inferred← citeshttps://doi.org/10.1007/s11829-024-10102-4openalex-snapshot
Pollination of Blumenbachia catharinensis (Loasaceae)—efficient pollen collection and pollen theft from the stigma by an oligolectic bee
inferred← citeshttps://doi.org/10.1007/s13127-016-0312-4openalex-snapshot
Diversification of Caiophora (Loasaceae subfam. Loasoideae) during the uplift of the Central Andes
inferred← citeshttps://doi.org/10.1007/s40415-016-0258-yopenalex-snapshot
Pollination of Aosa rupestris (Hook.) Weigend (Loasaceae): are stamen movements induced by pollinators?
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2013.02.002openalex-snapshot
Systemic resistance and growth promotion of chili pepper induced by an antibiotic producing Bacillus vallismortis strain BS07
inferred← citeshttps://doi.org/10.1016/j.bjbas.2018.07.004openalex-snapshot
Comparative morphological study of three species of Saraca L. (Fabaceae) by the statistical approach to find out the logic of potent morphological markers
inferred← citeshttps://doi.org/10.1016/j.ppees.2016.02.004openalex-snapshot
Plant–pollinator co-evolution: It's time to reconnect with Optimal Foraging Theory and Evolutionarily Stable Strategies
inferred← citeshttps://doi.org/10.1016/j.scienta.2011.05.031openalex-snapshot
Pollination studies in large cardamom (Amomum subulatum Roxb.) of Sikkim Himalayan region of India
inferred← citeshttps://doi.org/10.1016/j.tplants.2007.06.009openalex-snapshot
Hummingbirds as drivers of plant speciation?
inferred← citeshttps://doi.org/10.1038/s41598-018-32384-4openalex-snapshot
A case of behavioural diversification in male floral function – the evolution of thigmonastic pollen presentation
inferred← citeshttps://doi.org/10.1038/s41598-019-53853-4openalex-snapshot
Geography is essential for reproductive isolation between florally diversified morning glory species from Amazon canga savannahs
inferred← citeshttps://doi.org/10.1086/523358openalex-snapshot
Evolutionary Transitions in Floral Color
inferred← citeshttps://doi.org/10.1086/690023openalex-snapshot
Great Expectations: Correlations between Pollinator Assemblages and Floral Characters in Lamiaceae
inferred← citeshttps://doi.org/10.1093/aob/mcw035openalex-snapshot
Exploring the ontogenetic scaling hypothesis during the diversification of pollination syndromes inCaiophora(Loasaceae, subfam. Loasoideae)
inferred← citeshttps://doi.org/10.1093/biolinnean/bly061openalex-snapshot
Pollination of Blumenbachia amana (Loasaceae): flower morphology and partitioned pollen presentation guarantee a private reward to a specialist pollinator
inferred← citeshttps://doi.org/10.1093/botlinnean/boab068openalex-snapshot
Changes in floral shape: insights into the evolution of wild Nicotiana (Solanaceae)
inferred← citeshttps://doi.org/10.1101/2023.12.01.569612openalex-snapshot
Genome-wide SNP data reveal recent population structure of Huidobria fruticosa (Loasaceae), a paleo-endemic lineage from the Atacama Desert
inferred← citeshttps://doi.org/10.1111/brv.13094openalex-snapshot
Macroevolution of the plant–hummingbird pollination system
inferred← citeshttps://doi.org/10.1111/ede.12246openalex-snapshot
The evolution of floral ontogenetic allometry in the Andean genusCaiophora(Loasaceae, subfam. Loasoideae)
inferred← citeshttps://doi.org/10.1111/j.0030-1299.2007.16029.xopenalex-snapshot
Effects of phenotypic complementarity and phylogeny on the nested structure of mutualistic networks
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2010.01419.xopenalex-snapshot
Reloading the revolver - male fitness as a simple explanation for complex reward partitioning in Nasa macrothyrsa (Loasaceae, Cornales)
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2010.01036.xopenalex-snapshot
Variation in nectar-sugar profile of Anchusa and allied genera (Boraginaceae)
inferred← citeshttps://doi.org/10.1111/j.1365-2435.2012.02017.xopenalex-snapshot
Foraging rules of flower selection applied by colonies of A pis mellifera: ranking and associations of floral sources
inferred← citeshttps://doi.org/10.1111/j.1558-5646.2008.00398.xopenalex-snapshot
IS FLORAL SPECIALIZATION AN EVOLUTIONARY DEAD‐END? POLLINATION SYSTEM TRANSITIONS INRUELLIA(ACANTHACEAE)
inferred← citeshttps://doi.org/10.1111/nph.18464openalex-snapshot
Evolutionary convergence on hummingbird pollination in Neotropical Costus provides insight into the causes of pollinator shifts
inferred← citeshttps://doi.org/10.1111/plb.12225openalex-snapshot
Pollination syndromes in a specialised plant‐pollinator interaction: does floral morphology predict pollinators in C alceolaria?
inferred← citeshttps://doi.org/10.1111/plb.13072openalex-snapshot
Specialised protagonists in a plant–pollinator interaction: the pollination of Blumenbachia insignis (Loasaceae)
inferred← citeshttps://doi.org/10.1139/cjb-2020-0163openalex-snapshot
Preliminary observations on the flower visitors of Nasa colanii (Loasaceae), a poorly known species endemic to northern Peru
inferred← citeshttps://doi.org/10.11606/t.41.2010.tde-24112010-093628openalex-snapshot
Evolução da morfologia floral e estrutura de comunidades em um clado de Lianas Tropicais (Bignonieae, Bignoniaceae)
inferred← citeshttps://doi.org/10.11646/phytotaxa.203.1.1openalex-snapshot
Revisions in the South American Calandrinia caespitosa complex (Montiaceae)
inferred← citeshttps://doi.org/10.11646/zootaxa.5404.1.14openalex-snapshot
A new neopasiphaeine bee associated with flowers of Loasaceae (Hymenoptera: Colletidae: Actenosigynes)
inferred← citeshttps://doi.org/10.1186/s13227-021-00186-xopenalex-snapshot
Delayed differentiation of epidermal cells walls can underlie pedomorphosis in plants: the case of pedomorphic petals in the hummingbird-pollinated Caiophora hibiscifolia (Loasaceae, subfam. Loasoideae) species
inferred← citeshttps://doi.org/10.1186/s42269-022-00957-zopenalex-snapshot
Chemical characterization and antimicrobial activity of Blumenbachia insignis (Loasaceae) native to South America
inferred← citeshttps://doi.org/10.12705/662.5openalex-snapshot
Phylogenetic relationships and generic re‐arrangements in “South Andean Loasas” (Loasaceae)
inferred← citeshttps://doi.org/10.1371/journal.pone.0041121openalex-snapshot
Total Control – Pollen Presentation and Floral Longevity in Loasaceae (Blazing Star Family) Are Modulated by Light, Temperature and Pollinator Visitation Rates
inferred← citeshttps://doi.org/10.1590/0001-3765202120191446openalex-snapshot
Rethinking the pollination syndromes in Hymenaea (Leguminosae): the role of anthesis in the diversification
inferred← citeshttps://doi.org/10.1657/1938-4246-43.3.410openalex-snapshot
Difference in Floral Traits, Pollination, and Reproductive Success between White and Blue Flowers ofGentiana leucomelaena(Gentianaceae) in an Alpine Meadow
inferred← citeshttps://doi.org/10.26786/1920-7603(2016)5openalex-snapshot
Floral longevity, nectar production, pollen release, and stigma receptivity in Haskap (Lonicera caerulea)
inferred← citeshttps://doi.org/10.3389/fpls.2018.01100openalex-snapshot
Nectar Analysis Throughout the Genus Nicotiana Suggests Conserved Mechanisms of Nectar Production and Biochemical Action
inferred← citeshttps://doi.org/10.3390/metabo10050214openalex-snapshot
Metabolomic Profiling of Nicotiana Spp. Nectars Indicate That Pollinator Feeding Preference Is a Stronger Determinant Than Plant Phylogenetics in Shaping Nectar Diversity
inferred← citeshttps://doi.org/10.3390/plants10030507openalex-snapshot
Evolutionary and Ecological Considerations on Nectar-Mediated Tripartite Interactions in Angiosperms and Their Relevance in the Mediterranean Basin
inferred← citeshttps://doi.org/10.3398/064.085.0308openalex-snapshot
Pollination Biology of an Endemic Utah Wildflower, Penstemon sepalulus
inferred← citeshttps://doi.org/10.35249/rche.45.3.19.20openalex-snapshot
Actividad de visita de abejas nativas (Hymenoptera: Apoidea) hacia Loasa tricolor Ker-Gawl. (Loasaceae) en relación con temperatura ambiental y recursos florales
inferred← citeshttps://doi.org/10.3732/ajb.0900182openalex-snapshot
Evolution of floral morphology and pollination system in Bignonieae (Bignoniaceae)
inferred← citeshttps://doi.org/10.3732/ajb.2007403openalex-snapshot
Hybridization and crossability in Caiophora (Loasaceae subfam. Loasoideae): Are interfertile species and inbred populations results of a recent radiation?
inferred← citeshttps://doi.org/10.3897/phytokeys.222.98139openalex-snapshot
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inferred← citeshttps://doi.org/10.3897/phytokeys.47.8347openalex-snapshot
Plant endemism in the Sierras of Córdoba and San Luis (Argentina): understanding links between phylogeny and regional biogeographical patterns1
inferred← citeshttps://doi.org/10.4257/oeco.2010.1401.03openalex-snapshot
BEYOND HUMMINGBIRD-FLOWERS: THE OTHER SIDE OF ORNITHOPHILY IN THE NEOTROPICS
inferred← citeshttps://doi.org/10.55730/1300-011x.3086openalex-snapshot
The molecular regulators, pathways, and environmental impacts of white flowers
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