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Nectar-secreting Floral Stomata in Maxillaria anceps Ames & C. Schweinf. (Orchidaceae)

https://doi.org/10.1093/aob/mci182
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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.1537-2197.1980.tb07670.xopenalex-snapshot
STRUCTURE OF FLORAL NECTARIES OF ALFALFA (MEDICAGO SATIVA L.) IN RELATION TO NECTAR PRODUCTION
inferredcites →https://doi.org/10.1006/anbo.1996.0112openalex-snapshot
Ultrastructure and Function of Floral Nectaries ofChamelaucium uncinatum(Myrtaceae)
inferredcites →https://doi.org/10.1006/anbo.1997.0546openalex-snapshot
The Floral Nectary ofDigitalis purpureaL., Structure and Nectar Secretion
inferredcites →https://doi.org/10.1006/anbo.2000.1154openalex-snapshot
Pseudopollen: Its Structure and Development in Maxillaria(Orchidaceae)
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/10.1006/bojl.1997.0160openalex-snapshot
Ultrastructure of the labellar epidermis in selected Maxillaria species (Orchidaceae)
inferredcites →https://doi.org/10.1007/978-3-7091-6306-1_14openalex-snapshot
Deceptive orchids with meliponini as pollinators
inferredcites →https://doi.org/10.1007/bf00379082openalex-snapshot
Nectar selection by Melipona and Apis mellifera (Hymenoptera: Apidae) and the ecology of nectar intake by bee colonies in a tropical forest
inferredcites →https://doi.org/10.1007/bf00984106openalex-snapshot
Deceptive orchids with Meliponini as pollinators
inferredcites →https://doi.org/10.1007/bf01279253openalex-snapshot
Anatomical and ultrastructural changes of the floral nectary ofPisum sativum L. during flower development
inferredcites →https://doi.org/10.1007/bf02506798openalex-snapshot
Nectar, nectaries, flower visitors, and breeding system in five terrestrial Orchidaceae from central Argentina
inferredcites →https://doi.org/10.1007/s004250050070openalex-snapshot
Lectin and alliinase are the predominant proteins in nectar from leek (Allium porrum L.) flowers
inferredcites →https://doi.org/10.1007/s004250050325openalex-snapshot
Nectar-carbohydrate production and composition vary in relation to nectary anatomy and location within individual flowers of several species of Brassicaceae
inferredcites →https://doi.org/10.1007/s004420050113openalex-snapshot
Evidence for widespread pollen limitation of fruiting success in Cape wildflowers
inferredcites →https://doi.org/10.1007/s00606-002-0269-yopenalex-snapshot
Nectar sugar composition in angiosperms from Chaco and Patagonia (Argentina): an animal visitor's matter?
inferredcites →https://doi.org/10.1007/s00606-002-0275-0openalex-snapshot
Variability of nectar production and composition in Linaria vulgaris (L.) Mill. (Scrophulariaceae)
inferredcites →https://doi.org/10.1007/s00606-002-0279-9openalex-snapshot
Floral nectary ultrastructure of Prunus persica (L.) Batch cv. Forastero (Newcomer), an Argentine peach
inferredcites →https://doi.org/10.1007/s00606-002-0283-0openalex-snapshot
Characteristics of floral nectaries and nectar in two species of Crataegus (Rosaceae)
inferredcites →https://doi.org/10.1007/s00606-003-0276-7openalex-snapshot
Nectar as food for birds: the physiological consequences of drinking dilute sugar solutions
inferredcites →https://doi.org/10.1007/s006060170036openalex-snapshot
Hawkmoth pollination of the African epiphytic orchid Mystacidium venosum , with special reference to flower and pollen longevity
inferredcites →https://doi.org/10.1016/0378-4347(91)80245-8openalex-snapshot
High-performance liquid chromatography in enzymatic analysis
inferredcites →https://doi.org/10.1016/b978-0-12-583980-8.50011-9openalex-snapshot
Pollinator–Plant Interactions and the Evolution of Breeding Systems
inferredcites →https://doi.org/10.1016/s0065-2296(00)31006-0openalex-snapshot
Structure and function of secretory cells
inferredcites →https://doi.org/10.1016/s0065-2296(08)60332-8openalex-snapshot
Plant Resins—Their Formation, Secretion and Possible Functions
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/s0305-1978(99)00029-0openalex-snapshot
Floral nectar chemical composition of some species from Patagonia. II
inferredcites →https://doi.org/10.1023/a:1026164922760openalex-snapshot
Autofluorescence of Plant Secreting Cells as a Biosensor and Bioindicator Reaction
inferredcites →https://doi.org/10.1023/b:joec.0000028466.50392.edopenalex-snapshot
The Chemistry of Pollination in Selected Brazilian Maxillariinae Orchids: Floral Rewards and Fragrance
inferredcites →https://doi.org/10.1046/j.1095-8339.2003.00219.xopenalex-snapshot
Atypical pseudopollen-forming hairs in Maxillaria (Orchidaceae)
inferredcites →https://doi.org/10.1051/apido:19860205openalex-snapshot
AMINO ACID AND SUGAR CONTENT OF THE NECTAR EXUDATE FROM LIMODORUM ABORTIVUM (ORCHIDACEAE). COMPARISON WITH EPIPACTIS ATROPURPUREA NECTAR COMPOSITION
inferredcites →https://doi.org/10.1051/apido:19940612openalex-snapshot
Floral nectaries from Limodorum abortivum (L) Sw and Epipactis atropurpurea Rafin (Orchidaceae): ultrastructural changes in plastids during the secretory process
inferredcites →https://doi.org/10.1051/apido:19970104openalex-snapshot
Influence of floral visitation on nectar-sugar composition and nectary surface changes in Eucalyptus
inferredcites →https://doi.org/10.1051/apido:19990106openalex-snapshot
Nectar foraging by stingless bees in Costa Rica: botanical and climatological influences on sugar concentration of nectar collected by Melipona
inferredcites →https://doi.org/10.1080/0021213x.1990.10677140openalex-snapshot
THE PREDICTIVE VALUE OF NECTAR CHEMISTRY TO THE RECOGNITION OF POLLINATOR TYPES
inferredcites →https://doi.org/10.1086/407484openalex-snapshot
The Role of Trichomes in Plant Defense
inferredcites →https://doi.org/10.1093/aob/mcg038openalex-snapshot
Lipoidal Labellar Secretions in Maxillaria Ruiz & Pav. (Orchidaceae)
inferredcites →https://doi.org/10.1093/aob/mch007openalex-snapshot
Morphology of Floral Papillae in Maxillaria Ruiz & Pav. (Orchidaceae)
inferredcites →https://doi.org/10.1093/aob/mch008openalex-snapshot
Nectary Structure and Nectar Secretion in Maxillaria coccinea (Jacq.) L.O. Williams ex Hodge (Orchidaceae)
inferredcites →https://doi.org/10.1093/aob/mch009openalex-snapshot
Pollinarium Morphology and Floral Rewards inBrazilian Maxillariinae (Orchidaceae)
inferredcites →https://doi.org/10.1093/aob/mch072openalex-snapshot
Lip Anatomy and its Implications for the Pollination Mechanisms of Bulbophyllum Species (Orchidaceae)
inferredcites →https://doi.org/10.1093/aob/mch137openalex-snapshot
Floral Nectaries, Nectar Production Dynamics and Chemical Composition in Six Ipomoea Species (Convolvulaceae) in Relation to Pollinators
inferredcites →https://doi.org/10.1093/aob/mci081openalex-snapshot
Comparative Account of Nectary Structure in Hexisea imbricata (Lindl.) Rchb.f. (Orchidaceae)
inferredcites →https://doi.org/10.1104/pp.96.3.675openalex-snapshot
Secreting Glandular Trichomes: More than Just Hairs
inferredcites →https://doi.org/10.1111/j.1095-8339.1998.tb02087.xopenalex-snapshot
Comparative anatomy and systematics of Senghas's cushion species of Maxillaria (Orchidaceae)
inferredcites →https://doi.org/10.1111/j.1095-8339.1999.tb00768.xopenalex-snapshot
The pollination mechanism in the «Pelexia alliance» (Orchidaceae: Spiranthinae)
inferredcites →https://doi.org/10.1111/j.1438-8677.1886.tb04346.xopenalex-snapshot
32. J. M. Janse: Imitirte Pollenkörner bei Maxillaria sp
inferredcites →https://doi.org/10.1111/j.1469-8137.1961.tb06255.xopenalex-snapshot
TYPES OF NECTAR IN ANGIOSPERMS
inferredcites →https://doi.org/10.1111/j.1469-8137.1970.tb04062.xopenalex-snapshot
SUGAR CONTENT IN FLORAL AND EXTRAFLORAL EXUDATES OF ORCHIDS: POLLINATION, MYRMECOLOGY AND CHEMOTAXONOMY IMPLICATION
inferredcites →https://doi.org/10.1126/science.189.4201.476openalex-snapshot
Nectar Fluorescence under Ultraviolet Irradiation
inferredcites →https://doi.org/10.1146/annurev.es.06.110175.001035openalex-snapshot
Energetics of Pollination
inferredcites →https://doi.org/10.15517/lank.v3i2.23016openalex-snapshot
Toward a phylogeny of Maxillariinae orchids: multidisciplinary studies with emphasis in Brazilian species
inferredcites →https://doi.org/10.17660/actahortic.1991.288.53openalex-snapshot
THE MODIFIED STOMATA OF THE FLORAL NECTARY OF VICIA FABA L. 2. STOMATAL NUMBER AND DISTRIBUTION AS SELECTION CRITERIA FOR BREEDING FOR HIGH NECTAR SUGAR PRODUCTION
inferredcites →https://doi.org/10.2307/1216299openalex-snapshot
Strasburger's Textbook of Botany
inferredcites →https://doi.org/10.2307/1219717openalex-snapshot
The Orchids: Natural History and Classification
inferredcites →https://doi.org/10.2307/2446499openalex-snapshot
Fruit set, nectar reward, and rarity in the Orchidaceae
inferredcites →https://doi.org/10.2307/2656837openalex-snapshot
Subtribal and generic relationships of Maxillarieae (Orchidaceae) with emphasis on Stanhopeinae: combined molecular evidence

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.5091/plecevo.124295zenodo-depositor-declared
Fluorescent nectar in non-flying mammal-pollinated plants – observations and considerations in some Asparagaceae
inferred← citeshttps://doi.org/10.1002/ajb2.1849openalex-snapshot
Evidence of floral rewards in Brasiliorchis supports the convergent evolution of food‐hairs in Maxillariinae
inferred← citeshttps://doi.org/10.1007/978-1-4020-5937-7_2openalex-snapshot
A systematic survey of floral nectaries
inferred← citeshttps://doi.org/10.1007/978-1-4020-8802-5_4openalex-snapshot
Morphology
inferred← citeshttps://doi.org/10.1007/s00114-010-0709-4openalex-snapshot
Is the flower fluorescence relevant in biocommunication?
inferred← citeshttps://doi.org/10.1007/s00468-016-1504-4openalex-snapshot
Relationship between the morphological structure of floral nectaries and the formation, transport, and secretion of nectar in lychee
inferred← citeshttps://doi.org/10.1007/s00606-010-0294-1openalex-snapshot
Morphological and histological characterization of the osmophores and nectaries of four species of Acianthera (Orchidaceae: Pleurothallidinae)
inferred← citeshttps://doi.org/10.1007/s00606-012-0609-5openalex-snapshot
Secretion and composition of nectar and the structure of perigonal nectaries in Fritillaria meleagris L. (Liliaceae)
inferred← citeshttps://doi.org/10.1007/s00606-012-0740-3openalex-snapshot
Anatomy of the floral nectaries of some neotropical Salacioideae (Celastraceae)
inferred← citeshttps://doi.org/10.1007/s00606-013-0978-4openalex-snapshot
Anatomical and developmental studies on floral nectaries in Cardiospermum species: an approach to the evolutionary trend in Paullinieae
inferred← citeshttps://doi.org/10.1007/s00709-014-0668-2openalex-snapshot
Studies on floral nectary, tepals’ structure, and gynostemium morphology of Epipactis palustris (L.) Crantz (Orchidaceae)
inferred← citeshttps://doi.org/10.1007/s00709-018-1274-5openalex-snapshot
Floral nectary and osmophore of Epipactis helleborine (L.) Crantz (Orchidaceae)
inferred← citeshttps://doi.org/10.1007/s00709-018-1330-1openalex-snapshot
Comparative survey of secretory structures and floral anatomy of Cohniella cepula and Cohniella jonesiana (Orchidaceae: Oncidiinae). New evidences of nectaries and osmophores in the genus
inferred← citeshttps://doi.org/10.1007/s00709-019-01433-8openalex-snapshot
Flower nectar trichome structure of carnivorous plants from the genus butterworts Pinguicula L. (Lentibulariaceae)
inferred← citeshttps://doi.org/10.1007/s00709-020-01498-wopenalex-snapshot
Localization, morphology, anatomy and ultrastructure of osmophores in species of Rhamnaceae
inferred← citeshttps://doi.org/10.1007/s00709-025-02142-1openalex-snapshot
Morphology, anatomy and ultrastructure of petals in Alicia anisopetala and Callaeum psilophyllum (Malpighiaceae): implications for pollinator attraction
inferred← citeshttps://doi.org/10.1007/s10886-025-01611-4openalex-snapshot
Cyclopogon guayanensis is an Unusual Orchid with a Generalistic Pollination System and Hexose Dominant Nectar
inferred← citeshttps://doi.org/10.1007/s40415-018-0469-5openalex-snapshot
Anatomical analyses of floral and extrafloral secreting structures indicate the presence of nectaries and colleters in Stanhopea grandiflora Lindl.
inferred← citeshttps://doi.org/10.1007/s40415-019-00516-3openalex-snapshot
Labellar secretion and secretory trichomes of Rhetinantha cerifera (Barb. Rodr.) M.A.Blanco (Orchidaceae, Maxillariinae): micromorphology and composition
inferred← citeshttps://doi.org/10.1016/j.flora.2011.10.006openalex-snapshot
Two structures and functions in the nectary of Frankincense tree (Boswellia sacra Flueck.)
inferred← citeshttps://doi.org/10.1016/j.flora.2014.03.002openalex-snapshot
Anatomy and histochemistry of the nectaries of Rodriguezia venusta (Lindl.) Rchb. f. (Orchidaceae)
inferred← citeshttps://doi.org/10.1016/j.flora.2015.11.002openalex-snapshot
Late stages of anther development and anther attributes in Microepidendrum differs from other genera of Epidendrum alliance (Orchidaceae)
inferred← citeshttps://doi.org/10.1016/j.flora.2022.152179openalex-snapshot
Floral gland diversity in Pleurothallidinae (Epidendroideae–Orchidaceae)
inferred← citeshttps://doi.org/10.1038/s41598-022-09146-4openalex-snapshot
Ornithophily in the subtribe Maxillariinae (Orchidaceae) proven with a case study of Ornithidium fulgens in Guatemala
inferred← citeshttps://doi.org/10.1038/s41598-024-62626-7openalex-snapshot
Shining a light on UV-fluorescent floral nectar after 50 years
inferred← citeshttps://doi.org/10.1071/bt06193openalex-snapshot
Flowering phenology, nectary structure and breeding system in Corymborkis flava (Spiranthoideae:Tropidieae), a terrestrial orchid from a Neotropical forest
inferred← citeshttps://doi.org/10.1071/bt08135openalex-snapshot
Bees and white spiders: unravelling the pollination syndrome of Caladenia rigida (Orchidaceae)
inferred← citeshttps://doi.org/10.1071/bt23110openalex-snapshot
Pollination by multiple species of nectar foraging Hymenoptera in Prasophyllum innubum, a critically endangered orchid of the Australian Alps
inferred← citeshttps://doi.org/10.1093/aob/mcad178openalex-snapshot
Sexual attraction with pollination during feeding behaviour: implications for transitions between specialized strategies
inferred← citeshttps://doi.org/10.1093/aob/mcl065openalex-snapshot
A Rudimentary Labellar Speculum in Cymbidium lowianum (Rchb.f.) Rchb.f. and Cymbidium devonianum Paxton (Orchidaceae)
inferred← citeshttps://doi.org/10.1093/aob/mcl204openalex-snapshot
Labellar Micromorphology of Bifrenariinae Dressler (Orchidaceae)
inferred← citeshttps://doi.org/10.1093/aob/mcm165openalex-snapshot
Micromorphology of the Labellum and Floral Spur of Cryptocentrum Benth. and Sepalosaccus Schltr. (Maxillariinae: Orchidaceae)
inferred← citeshttps://doi.org/10.1093/aob/mct197openalex-snapshot
The evolution of floral nectaries in Disa (Orchidaceae: Disinae): recapitulation or diversifying innovation?
inferred← citeshttps://doi.org/10.1093/aobpla/plac039openalex-snapshot
Coryanthes macrantha(Orchidaceae: Stanhopeinae) and their floral and extrafloral secretory structures: an anatomical and phytochemical approach
inferred← citeshttps://doi.org/10.1093/botlinnean/boaa074openalex-snapshot
Novelties in the secretory structures of three species ofGongora(Orchidaceae: Stanhopeinae)
inferred← citeshttps://doi.org/10.1093/botlinnean/boaa095openalex-snapshot
Floral micromorphology, histochemistry, ultrastructure and chemical composition of floral secretions in three Neotropical Maxillariella species (Orchidaceae)
inferred← citeshttps://doi.org/10.1093/botlinnean/boab093openalex-snapshot
Untold diversity of floral rewards inCypella(Tigridieae: Iridaceae) and related genera: distribution and anatomy
inferred← citeshttps://doi.org/10.1093/botlinnean/boy058openalex-snapshot
Pollination by nectar-foraging thynnine wasps: evidence of a new specialized pollination system for Australian orchids
inferred← citeshttps://doi.org/10.1093/botlinnean/boz013openalex-snapshot
Comparative anatomy of putative secretory floral structures in the Camaridium cucullatum complex and Nitidobulbon (Orchidaceae: Maxillariinae)
inferred← citeshttps://doi.org/10.1093/hr/uhad249openalex-snapshot
Vacuolar proteomic analysis reveals tonoplast transporters for accumulation of citric acid and sugar in citrus fruit
inferred← citeshttps://doi.org/10.1093/jpe/rtq012openalex-snapshot
Generalized food-deceptive orchid species flower earlier and occur at lower altitudes than rewarding ones
inferred← citeshttps://doi.org/10.1111/boj.12024openalex-snapshot
Anatomy of the floral nectary of ornithophilousElleanthus brasiliensis(Orchidaceae: Sobralieae)
inferred← citeshttps://doi.org/10.1111/boj.12094openalex-snapshot
Dual deceit in pseudopollen-producingMaxillaria s.s.(Orchidaceae: Maxillariinae)
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2007.00681.xopenalex-snapshot
Elaiophore diversity in three contrasting members of Oncidiinae (Orchidaceae)
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2012.01278.xopenalex-snapshot
Comparative labellar anatomy of resin-secreting and putative resin-mimic species ofMaxillaria s.l. (Orchidaceae: Maxillariinae)
inferred← citeshttps://doi.org/10.1111/plb.12312openalex-snapshot
Pollination ecology of two species of Elleanthus (Orchidaceae): novel mechanisms and underlying adaptations to hummingbird pollination
inferred← citeshttps://doi.org/10.1139/b09-109openalex-snapshot
Floral nectary structure, nectar production, and carbohydrate composition in theLiliumAsiatic hybrid ‘Trésor’
inferred← citeshttps://doi.org/10.1186/s12870-022-03944-8openalex-snapshot
Floral attractants in the black orchid Brasiliorchis schunkeana (Orchidaceae, Maxillariinae): clues for presumed sapromyophily and potential antimicrobial activity
inferred← citeshttps://doi.org/10.1186/s43897-021-00008-7openalex-snapshot
Multiple functions of the vacuole in plant growth and fruit quality
inferred← citeshttps://doi.org/10.17129/botsci.2785openalex-snapshot
Pollination success in three tropical dry forest orchid species from Mexico: insights from floral display, visitation rates, and flower micromorphology
inferred← citeshttps://doi.org/10.2985/026.019.0102openalex-snapshot
Embryology and Seed Development inPereskia lychnidiflora(Cactaceae)
inferred← citeshttps://doi.org/10.3389/fpls.2018.00840openalex-snapshot
Nectar-Secreting and Nectarless Epidendrum: Structure of the Inner Floral Spur
inferred← citeshttps://doi.org/10.3389/fpls.2020.00249openalex-snapshot
Floral Humidity in Flowering Plants: A Preliminary Survey
inferred← citeshttps://doi.org/10.3390/biology11060887openalex-snapshot
Application of Optical Fluorescence Spectroscopy for Studying Bee Abundance in Tropaeolum majus L. (Tropaeolaceae)
inferred← citeshttps://doi.org/10.3390/d13110533openalex-snapshot
Comparative Floral and Pollen Micromorphology of Leonurus japonicus and L. macranthus (Lamiaceae)
inferred← citeshttps://doi.org/10.3390/ecologies7030062openalex-snapshot
Reproductive Ecology of Maxillaria carinulata and Maxillaria meridensis (Orchidaceae) in the Andes of Caquetá, Colombia: Breeding System, Floral Visitors, Floral Compounds, and Pollen Transfer
inferred← citeshttps://doi.org/10.3390/plants10112315openalex-snapshot
Floral Nectar Chemistry in Orchids: A Short Review and Meta-Analysis
inferred← citeshttps://doi.org/10.3390/plants12040921openalex-snapshot
Labellar Structure of the Maxillaria splendens Alliance (Orchidaceae: Maxillariinae) Indicates Floral Polyphenols as a Reward for Stingless Bees
inferred← citeshttps://doi.org/10.3732/ajb.94.11.1860openalex-snapshot
Molecular phylogenetics of Maxillaria and related genera (Orchidaceae: Cymbidieae) based on combined molecular data sets
inferred← citeshttps://doi.org/10.3897/phytokeys.190.77918openalex-snapshot
Maxillaria anacatalinaportillae (Orchidaceae, Maxillariinae), a new remarkable species from Ecuador
inferred← citeshttps://doi.org/10.4236/abb.2013.43042openalex-snapshot
An assessment of factors leading to the decline of Beclardia macrostachya (orchidaceae) population in Mauritius
inferred← citeshttps://doi.org/10.55360/cpn494.mg117openalex-snapshot
First observations of UV-induced fluorescence in Heliamphora (Sarraceniaceae) and other tepui flora
inferred← citeshttps://doi.org/10.5586/aa.2009.021openalex-snapshot
Nectary structure of Ornithidium sophronitis Rchb.F. (Orchidaceae: Maxillariinae)
inferred← citeshttps://doi.org/10.5586/aa.2010.001openalex-snapshot
Structure of the cuniculus nectary in Brassavola flagellaris Barb. Rodr. (Laeliinae Benth., Orchidaceae)
inferred← citeshttps://doi.org/10.5897/ajb10.2248openalex-snapshot
Dynamic changes of stomatal characteristics during the flower, fruit and leaf developments of Zephyranthes candida (Lindl.) Herb
inferred← citeshttps://doi.org/10.6084/m9.figshare.22608496openalex-snapshot
Additional file 1 of Floral attractants in the black orchid Brasiliorchis schunkeana (Orchidaceae, Maxillariinae): clues for presumed sapromyophily and potential antimicrobial activity
inferred← citeshttps://doi.org/10.6084/m9.figshare.22608499openalex-snapshot
Additional file 2 of Floral attractants in the black orchid Brasiliorchis schunkeana (Orchidaceae, Maxillariinae): clues for presumed sapromyophily and potential antimicrobial activity
inferred← citeshttps://doi.org/10.6084/m9.figshare.22608502openalex-snapshot
Additional file 3 of Floral attractants in the black orchid Brasiliorchis schunkeana (Orchidaceae, Maxillariinae): clues for presumed sapromyophily and potential antimicrobial activity
inferred← citeshttps://doi.org/10.6084/m9.figshare.22608505openalex-snapshot
Additional file 4 of Floral attractants in the black orchid Brasiliorchis schunkeana (Orchidaceae, Maxillariinae): clues for presumed sapromyophily and potential antimicrobial activity
inferred← citeshttps://doi.org/10.7235/hort.20190075openalex-snapshot
Floral Volatile Compound Accumulation and Gene Expression Analysis of Maxillaria tenuifolia
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