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Links between early pollen development and aperture pattern in monocots
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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.1537-2197.1988.tb11265.xopenalex-snapshot
MICROTUBULES ASSOCIATED WITH SIMULTANEOUS CYTOKINESIS OF COENOCYTIC MICROSPOROCYTES
inferredcites →https://doi.org/10.1002/j.1537-2197.1995.tb11569.xopenalex-snapshot
P ollen H eteromorphism in N icotiana tabacum (S olanaceae )
inferredcites →https://doi.org/10.1002/jez.10150openalex-snapshot
Aperture pattern ontogeny in angiosperms
inferredcites →https://doi.org/10.1006/anbo.1999.0942openalex-snapshot
Microsporogenesis in Monocotyledons
inferredcites →https://doi.org/10.1007/978-3-662-03531-3openalex-snapshot
Flowering Plants · Monocotyledons
inferredcites →https://doi.org/10.1007/bf00407003openalex-snapshot
Pollen wall formation in Lilium: The effect of chaotropic agents, and the organisation of the microtubular cytoskeleton during pattern development
inferredcites →https://doi.org/10.1007/s00606-003-0107-xopenalex-snapshot
Triaperturate pollen in the monocotyledons: configurations and conjectures
inferredcites →https://doi.org/10.1007/s00709-002-0075-yopenalex-snapshot
Postmeiotic cytokinesis and pollen aperture number determination in eudicots: effect of the cleavage wall number
inferredcites →https://doi.org/10.1016/b978-0-12-103458-0.50012-2openalex-snapshot
Pollen wall development in angiosperms
inferredcites →https://doi.org/10.1016/s0034-6667(98)90000-8openalex-snapshot
Pollen and spores: Morphology and biology
inferredcites →https://doi.org/10.1016/s0367-1615(17)31570-7openalex-snapshot
Zur vergleichenden Embryologie der Liliaceae-Asphodeloideae
inferredcites →https://doi.org/10.1016/s1369-5266(00)00132-1openalex-snapshot
The evolution of plant architecture
inferredcites →https://doi.org/10.1046/j.1095-8339.2003.t01-1-00158.xopenalex-snapshot
An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG II
inferredcites →https://doi.org/10.1071/9780643090149openalex-snapshot
Monocots: Systematics and Evolution
inferredcites →https://doi.org/10.1080/00173130152591877openalex-snapshot
Pollen aperture morphology in Arecaceae: Application within phylogenetic analyses, and a summary of record of palm-like pollen the fossil
inferredcites →https://doi.org/10.1080/00173136309437854openalex-snapshot
An Ultrastructural Study of Pollen Wall Ontogeny inSilene Pendula
inferredcites →https://doi.org/10.1080/11035895209453507openalex-snapshot
Pollen Morphology and Plant Taxonomy
inferredcites →https://doi.org/10.1086/323477openalex-snapshot
Equatorial Aperture Pattern in Monocots: Same Definition Rules as in Eudicots? The Example of Two Species of Pontederiaceae
inferredcites →https://doi.org/10.1093/aob/mci030openalex-snapshot
Multiple Developmental Pathways Leading to a Single Morph: Monosulcate Pollen (Examples From the Asparagales)
inferredcites →https://doi.org/10.1097/00010694-195303000-00016openalex-snapshot
Pollen Morphology and Plant Taxonomy
inferredcites →https://doi.org/10.1111/boj.12385openalex-snapshot
An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV
inferredcites →https://doi.org/10.1139/b97-044openalex-snapshot
Microsporogenesis and pollen sulcus type in Asparagales (Lilianae)
inferredcites →https://doi.org/10.1242/jcs.63.1.191openalex-snapshot
Determination of patterning in the pollen wall of Lilium henryi
inferredcites →https://doi.org/10.2307/2257057openalex-snapshot
Pollen-Morphology and Plant Taxonomy: Angiosperms.
inferredcites →https://doi.org/10.2307/2666681openalex-snapshot
Evolution, Variation, and Classification of Palms
inferredcites →https://doi.org/10.2307/4110220openalex-snapshot
Comparative External Pollen Ultrastructure of the Araceae and Putatively Related Taxa
inferredcites →https://doi.org/10.2307/4119375openalex-snapshot
Pollen and Spores: Morphology and Biology
inferredcites →https://doi.org/10.3732/ajb.92.4.576openalex-snapshot
Post‐meiotic cytokinesis and pollen aperture pattern ontogeny: comparison of development in four species differing in aperture pattern
inferredcites →https://doi.org/10.5962/p.276456openalex-snapshot
Pollen morphology of Madagascan Aristea and Geosiris (Iridaceae-Nivenioideae) in relation to systematics and phylogeny
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.350.3.3zenodo-depositor-declared
Embryology of Polygonatum (Asparagaceae) and its systematic significance
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0625openalex-snapshot
Exine and Aperture Patterns on the Pollen Surface: Their Formation and Roles in Plant Reproduction
inferred← citeshttps://doi.org/10.1002/jemt.23015openalex-snapshot
Identification of monocot flora using pollen features through scanning electron microscopy
inferred← citeshttps://doi.org/10.1002/jemt.23179openalex-snapshot
Palyno‐anatomical studies of monocot taxa and its taxonomic implications using light and scanning electron microscopy
inferred← citeshttps://doi.org/10.1007/978-3-319-71365-6_1openalex-snapshot
Palynology: History and Systematic Aspects
inferred← citeshttps://doi.org/10.1007/s00606-008-0001-7openalex-snapshot
Successive microsporogenesis in eudicots, with particular reference to Berberidaceae (Ranunculales)
inferred← citeshttps://doi.org/10.1007/s00606-017-1398-7openalex-snapshot
Embryology of Hemerocallis L. and its systematic significance
inferred← citeshttps://doi.org/10.1007/s00709-018-1282-5openalex-snapshot
Formation pattern in five types of pollen tetrad in Pseuduvaria trimera (Annonaceae)
inferred← citeshttps://doi.org/10.1007/s00709-023-01887-xopenalex-snapshot
Pollen wall development in Impatiens glandulifera: exine substructure and underlying mechanisms
inferred← citeshttps://doi.org/10.1007/s00709-024-01970-xopenalex-snapshot
Mechanisms of pollen wall development in Lysimachia vulgaris
inferred← citeshttps://doi.org/10.1007/s10722-024-02182-1openalex-snapshot
Pollen patterns and morphological variability unraveling cyperaceae diversity through palynological traits
inferred← citeshttps://doi.org/10.1016/b978-0-12-373971-1.00014-5openalex-snapshot
Callose and its Role in Pollen and Embryo Sac Development in Flowering Plants
inferred← citeshttps://doi.org/10.1038/s41477-020-0630-6openalex-snapshot
Rice pollen aperture formation is regulated by the interplay between OsINP1 and OsDAF1
inferred← citeshttps://doi.org/10.1071/sb13046openalex-snapshot
The trichotomosulcate asparagoids: pollen morphology of Hemerocallidaceae in relation to systematics and pollination biology
inferred← citeshttps://doi.org/10.1080/00173130902746466openalex-snapshot
Microsporogenesis is simultaneous in the early‐divergent grass Streptochaeta, but successive in the closest grass relative, Ecdeiocolea
inferred← citeshttps://doi.org/10.1080/00173131003650920openalex-snapshot
Sporoderm ontogeny inChamaedorea microspadix(Arecaceae): self-assembly as the underlying cause of development
inferred← citeshttps://doi.org/10.1086/518265openalex-snapshot
Evolution of Microsporogenesis in Palms (Arecaceae)
inferred← citeshttps://doi.org/10.1086/664716openalex-snapshot
Premeiotic Microsporocyte Cell Shape Influences Shape of Tetrads during Microsporogenesis
inferred← citeshttps://doi.org/10.1086/693108openalex-snapshot
Saportanthus, an Extinct Genus of Laurales from the Early Cretaceous of Portugal
inferred← citeshttps://doi.org/10.1093/aob/mcp160openalex-snapshot
Release of developmental constraints on tetrad shape is confirmed in inaperturate pollen of Potamogeton
inferred← citeshttps://doi.org/10.1093/aob/mcq152openalex-snapshot
The influence of tetrad shape and intersporal callose wall formation on pollen aperture pattern ontogeny in two eudicot species
inferred← citeshttps://doi.org/10.1093/aob/mct104openalex-snapshot
Variation of microsporogenesis in monocots producing monosulcate pollen grains
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2006.00525.xopenalex-snapshot
Variations in the microsporogenesis of monosulcate palm pollen
inferred← citeshttps://doi.org/10.1111/j.1420-9101.2012.02494.xopenalex-snapshot
Evolutionary stasis in Euphorbiaceae pollen: selection and constraints
inferred← citeshttps://doi.org/10.1111/j.1525-142x.2007.00183.xopenalex-snapshot
Constraints and selection: insights from microsporogenesis in Asparagales
inferred← citeshttps://doi.org/10.1111/nph.13578openalex-snapshot
Evolutionary stasis in pollen morphogenesis due to natural selection
inferred← citeshttps://doi.org/10.1155/2011/104736openalex-snapshot
Flowering Ecology of the Species of the Genus Hypoxidia (Hypoxidaceae: Asparagales)
inferred← citeshttps://doi.org/10.3390/d15080898openalex-snapshot
Ontogeny of Different Tetrad Types in the Single Microsporangium of Mitrephora tomentosa (Annonaceae)
inferred← citeshttps://doi.org/10.3732/ajb.0800110openalex-snapshot
Phylogenetic comparative analysis of microsporogenesis in angiosperms with a focus on monocots
inferred← citeshttps://doi.org/10.3732/ajb.0900264openalex-snapshot
Formation and function of a new pollen aperture pattern in angiosperms: The proximal sulcus of Tillandsia leiboldiana (Bromeliaceae)
inferred← citeshttps://doi.org/10.3732/ajb.1000195openalex-snapshot
Correlation between pollen aperture pattern and callose deposition in late tetrad stage in three species producing atypical pollen grains
inferred← citeshttps://doi.org/10.3897/phytokeys.38.7495openalex-snapshot
Pantoporate pollen in the Asteraceae (Vernonieae)
inferred← citeshttps://doi.org/10.47749/t/unicamp.2014.926902openalex-snapshot
Diversidade morfológica de políades em espécies de Mimosoideae (Leguminosae)
inferred← citeshttps://doi.org/10.5772/33788openalex-snapshot
Microsporogenesis, Pollen Mitosis and In Vitro Pollen Tube Growth in Leucojum aestivum (Amaryllidaceae)
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