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Floral Structure and Breeding Systems of Manglietia conifera Dandy (Magnoliaceae)

https://doi.org/10.3390/f10090756
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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.

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/anbo.1999.1067openalex-snapshot
The Evolution and Function of Stylar Polymorphisms in Flowering Plants
inferredcites →https://doi.org/10.1007/bf00045059openalex-snapshot
Flowering and fruiting phenology in the coastal shrublands of Doñana, south Spain
inferredcites →https://doi.org/10.1007/bf02858097openalex-snapshot
A survey of floral traits, breeding systems, floral visitors, and pollination systems of the angiosperms of the Juan Fernández Islands (Chile)
inferredcites →https://doi.org/10.1016/b978-0-12-583980-8.50018-1openalex-snapshot
Microbehavior and Macrostructure in Pollinator–Plant Interactions
inferredcites →https://doi.org/10.1016/j.cub.2006.07.068openalex-snapshot
Evolution of Plant Breeding Systems
inferredcites →https://doi.org/10.1038/35068635openalex-snapshot
Flexible style that encourages outcrossing
inferredcites →https://doi.org/10.1038/hdy.1991.76openalex-snapshot
The effect of the density of flowering individuals on the mating systems of nine tropical tree species
inferredcites →https://doi.org/10.1093/aob/mcg201openalex-snapshot
Floral Structure, Breeding System and Fruit-set in the Threatened Sub-shrub Tetratheca juncea Smith (Tremandraceae)
inferredcites →https://doi.org/10.1111/j.1461-0248.2011.01601.xopenalex-snapshot
Meta-analysis of phenotypic selection on flowering phenology suggests that early flowering plants are favoured
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03892.xopenalex-snapshot
Inflorescence architecture affects pollinator behaviour and mating success in Spiranthes sinensis (Orchidaceae)
inferredcites →https://doi.org/10.1111/j.1558-5646.1977.tb00979.xopenalex-snapshot
POLLEN-OVULE RATIOS: A CONSERVATIVE INDICATOR OF BREEDING SYSTEMS IN FLOWERING PLANTS
inferredcites →https://doi.org/10.1111/j.1744-7917.2012.01519.xopenalex-snapshot
Data Processing System (DPS) software with experimental design, statistical analysis and data mining developed for use in entomological research
inferredcites →https://doi.org/10.1111/plb.12200openalex-snapshot
Relative impact of mateversuspollinator availability on pollen limitation and outcrossing rates in a mass‐flowering species
inferredcites →https://doi.org/10.1111/plb.12905openalex-snapshot
Breeding systems in Balsaminaceae in relation to pollen/ovule ratio, pollination syndromes, life history and climate zone
inferredcites →https://doi.org/10.1126/science.1071617openalex-snapshot
Rapid Changes in Flowering Time in British Plants
inferredcites →https://doi.org/10.1155/2013/350157openalex-snapshot
Annual Variation in Flowering Phenology, Pollination, Mating System, and Pollen Yield in Two Natural Populations of Schima wallichii (DC.) Korth
inferredcites →https://doi.org/10.1360/biodiv.070294openalex-snapshot
Studies on plant–pollinator interaction and its significances
inferredcites →https://doi.org/10.2307/2407542openalex-snapshot
Pollen-Ovule Ratios: A Conservative Indicator of Breeding Systems in Flowering Plants
inferredcites →https://doi.org/10.3390/f8100404openalex-snapshot
The Floral Biology, Breeding System and Pollination Efficiency of Schima superba Gardn. et Champ. (Theaceae)
inferredcites →https://doi.org/10.3724/sp.j.1003.2010.011openalex-snapshot
The butterflyPieris rapaeresulting in the reproductive success of two transplanted orchids in a botanical garden
inferredcites →https://doi.org/10.3724/sp.j.1143.2009.07329openalex-snapshot
The Floral Syndrome and Its Pollination in Cynanchum otophyllum (Asclepiadaceae)
inferredcites →https://doi.org/10.3732/ajb.1600305openalex-snapshot
Flowering phenology, growth forms, and pollination syndromes in tropical dry forest species: Influence of phylogeny and abiotic factors
inferredcites →https://doi.org/10.3732/ajb.90.9.1333openalex-snapshot
Natural selection on floral traits of Lobelia (Lobeliaceae): spatial and temporal variation

What points at this work

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

inferred← citeshttps://doi.org/10.3897/phytokeys.277.195893zenodo-depositor-declared
If these aren’t genuine species, what are? An analysis of heterotypic synonyms contributes to 19 new names and 20 new combinations in Magnolia (Magnoliaceae). Part 2: New combinations
inferred← citeshttps://doi.org/10.5281/zenodo.21302402zenodo-depositor-declared
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112724openalex-snapshot
Outcrossing preference in Magnolia ×soulangeana 'Hongyun' is associated with differential stigmatic ROS accumulation regulated by MsFERONIA–MsROP2–MsROBHD module
inferred← citeshttps://doi.org/10.23869/bphjbr.26.2.20216openalex-snapshot
Floral biology and breeding system of endangered species: Parmentiera cereifera Seem. (Bignoniaceae)
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