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Multiple Developmental Pathways Leading to a Single Morph: Monosulcate Pollen (Examples From the Asparagales)

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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.1537-2197.1974.tb12329.xopenalex-snapshot

APERTURE EVOLUTION IN THE POLLEN OF PRIMITIVE ANGIOSPERMS

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/10.1007/978-3-642-61663-1openalex-snapshot

The Families of the Monocotyledons

inferredcites →https://doi.org/10.1007/978-94-009-0285-5_60openalex-snapshot

A study on microsporogenesis and ovule morphology in tropical African Anthericaceae and Asphodelaceae

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/bf02861086openalex-snapshot

Comparative morphology of monocot pollen and evolutionary trends of apertures and wall structures

inferredcites →https://doi.org/10.1007/s004250050438openalex-snapshot

Meiotic cytokinetic apparatus in the formation of the linear spore tetrads of Conocephalum japonicum (Bryophyta)

inferredcites →https://doi.org/10.1007/s00606-002-0221-1openalex-snapshot

Partially hydrated pollen: taxonomic distribution, ecological and evolutionary significance

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/10.1016/0034-6667(67)90041-3openalex-snapshot

Apertures of pollen grains and their evolution in angiosperms

inferredcites →https://doi.org/10.1016/0034-6667(92)90022-9openalex-snapshot

Pollen apertures, exine sculpturing and phylogeny in Iridaceae subfamily Iridoideae

inferredcites →https://doi.org/10.1016/j.tplants.2004.01.001openalex-snapshot

Pollen aperture evolution – a crucial factor for eudicot success?

inferredcites →https://doi.org/10.1038/374027a0openalex-snapshot

The origin and early diversification of angiosperms

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/10.1080/001731300750044609openalex-snapshot

Pollen morphology in the family Asphodelaceae (Asphodeleae, Kniphofieae)

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/10.1080/00173139609430497openalex-snapshot

Pollen morphology ofAsphodelusL. (Asphodelaceae): taxonomic and phylogenetic inferences at the infrageneric level

inferredcites →https://doi.org/10.1080/00721395.1970.9989697openalex-snapshot

The evolution of miospore polarity

inferredcites →https://doi.org/10.1080/11035895209453507openalex-snapshot

Pollen Morphology and Plant Taxonomy

inferredcites →https://doi.org/10.1086/317573openalex-snapshot

Pollen Diversity in Some Modern Magnoliids

inferredcites →https://doi.org/10.1086/338322openalex-snapshot

Evolution of Microsporogenesis in Angiosperms

inferredcites →https://doi.org/10.1111/j.1756-1051.1998.tb01867.xopenalex-snapshot

Pollen morphology and its evolutionary significance in Hemerocallis (Liliaceae)

inferredcites →https://doi.org/10.1139/b97-044openalex-snapshot

Microsporogenesis and pollen sulcus type in Asparagales (Lilianae)

inferredcites →https://doi.org/10.1242/jcs.103.4.1031openalex-snapshot

Control of division plane in normal and griseofulvin-treated microsporocytes of Magnolia

inferredcites →https://doi.org/10.1242/jcs.11.3.699openalex-snapshot

The Organization and Polarity of Pollen Mother Cells of Triticum Aestivum

inferredcites →https://doi.org/10.1560/mele-cwbh-dfam-q38qopenalex-snapshot

POLLEN MORPHOLOGY OF TURKISH IRIS L. (IRIDACEAE) WITH REFERENCE TO EVOLUTIONARY TRENDS AT THE INFRAGENERIC LEVEL

inferredcites →https://doi.org/10.2307/2395271openalex-snapshot

The Bases of Angiosperm Phylogeny: Palynology

inferredcites →https://doi.org/10.2307/2399736openalex-snapshot

Sulcus and Operculum Structure in the Pollen Grains of Iridaceae Subfamily Ixioideae

inferredcites →https://doi.org/10.3732/ajb.89.3.393openalex-snapshot

Correlated variation in microtubule distribution, callose deposition during male post‐meiotic cytokinesis, and pollen aperture number across Nicotiana species (Solanaceae)

inferredcites →https://doi.org/10.5962/bhl.part.24686openalex-snapshot

Cretaceous angiosperm pollen of the Atlantic coastal plain and its evolutionary significance

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/10.11646/phytotaxa.564.1.3zenodo-depositor-declared

Pollen morphology of the genus Hyacinthella (Asparagaceae) and Muscari azureum in Türkiye

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/10.1007/s00606-010-0280-7openalex-snapshot

Sporogenesis and gametogenesis in Agapanthus praecox Willd. orientalis (Leighton) Leighton and their systematic implications

inferred← citeshttps://doi.org/10.1007/s00606-011-0427-1openalex-snapshot

Embryology of Iris mandshurica Maxim. (Iridaceae) and its systematic relationships

inferred← citeshttps://doi.org/10.1007/s00606-012-0699-0openalex-snapshot

Pollen morphology and wall structure of Neotropical species of Herreria and Clara (Asparagaceae-Agavoideae) and its taxonomic implications

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/s00606-017-1486-8openalex-snapshot

Pollen morphology of selected species of the genera Chrysodracon and Dracaena (Asparagaceae, subfamily Nolinoideae) and its systematic implications

inferred← citeshttps://doi.org/10.1007/s00709-006-0164-4openalex-snapshot

Links between early pollen development and aperture pattern in monocots

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/10.1016/j.crvi.2009.02.001openalex-snapshot

Microsporogenesis variation in Codiaeum producing inaperturate pollen grain

inferred← citeshttps://doi.org/10.1016/j.hpj.2021.01.007openalex-snapshot

Comparative analysis of Wanjincheng orange leaf and root responses to ‘Candidatus liberibacter asiaticus’ infection using leaf-disc grafting

inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.110222openalex-snapshot

Formation of aperture sites on the pollen surface as a model for development of distinct cellular domains

inferred← citeshttps://doi.org/10.1016/j.plaphy.2007.10.010openalex-snapshot

Plants, MEN and SIN

inferred← citeshttps://doi.org/10.1016/j.revpalbo.2017.09.004openalex-snapshot

Ontogeny of permanent tetrads in Gardenia jasminoides (Rubiaceae) provides insight into pollen evolution

inferred← citeshttps://doi.org/10.1071/bt14229openalex-snapshot

Causes of infertility in the endangered Australian endemic plant Borya mirabilis (Boryaceae)

inferred← citeshttps://doi.org/10.1080/00087114.2017.1416450openalex-snapshot

Spontaneous occurrence of micronuclei in developing microspores ofAgave angustifoliaHaw. cultivar “Lineño” andA. tequilanaWeber cultivar “Azul” (Asparagales, Asparagaceae)

inferred← citeshttps://doi.org/10.1080/00173130701485191openalex-snapshot

Aperture variation in the pollen ofNelumbo(Nelumbonaceae)

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/10.1086/518265openalex-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/10.1093/aob/mcl115openalex-snapshot

The Unique Pollen Morphology of Duparquetia (Leguminosae: Caesalpinioideae): Developmental Evidence of Aperture Orientation Using Confocal Microscopy

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/boj.12191openalex-snapshot

Diversity and evolution of microsporogenesis in Bromeliaceae

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/10.11646/phytotaxa.34.1.1openalex-snapshot

A revision of the Andean wax palms, Ceroxylon (Arecaceae)

inferred← citeshttps://doi.org/10.15381/rpb.v15i3.2979openalex-snapshot

Novelties in the genus Ceroxylon (Arecaceae) from Peru, with description of a new species

inferred← citeshttps://doi.org/10.1590/s0102-33062013000400003openalex-snapshot

Hippeastrum species in areas of restinga in the state of Rio de Janeiro, Brazil: pollen characters

inferred← citeshttps://doi.org/10.1600/036364414x683895openalex-snapshot

Taxonomic Revision of the Dioscorea campestris Species Assemblage (Dioscoreaceae)

inferred← citeshttps://doi.org/10.22201/ib.20078706e.2011.1.368openalex-snapshot

Anatomía floral comparativa del género Polianthes (Agavaceae)

inferred← citeshttps://doi.org/10.3109/10520295.2011.649784openalex-snapshot

A new fluorescent staining method for callose of microspore mother cells during meiosis

inferred← citeshttps://doi.org/10.3159/1095-5674(2007)134[335:mamgij]2.0.co;2openalex-snapshot

Microsporogenesis and Male Gametogenesis in Jatropha Curcas L. (Euphorbiaceae)1

inferred← citeshttps://doi.org/10.3390/cells14191549openalex-snapshot

Arabinogalactan Proteins Mark the Generative Cell–Vegetative Cell Interface in Monocotyledonous Pollen Grains

inferred← citeshttps://doi.org/10.3390/d15040501openalex-snapshot

How Do Pollen Grains of Convallaria majalis L. Respond to Different Habitat Conditions?

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/10.3390/plants11030357openalex-snapshot

A Review of the Developmental Processes and Selective Pressures Shaping Aperture Pattern in Angiosperms

inferred← citeshttps://doi.org/10.3417/2014014openalex-snapshot

Evolution of Angiosperm Pollen. 3. Monocots1

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/10.4161/psb.23394openalex-snapshot

Cytokinesis in plant male meiosis

inferred← citeshttps://doi.org/10.47749/t/unicamp.2014.926902openalex-snapshot

Diversidade morfológica de políades em espécies de Mimosoideae (Leguminosae)

inferred← citeshttps://doi.org/10.5352/jls.2009.19.8.1016openalex-snapshot

Ultrastructural Study of Programmed Cell Death of Tapetum In Panax ginseng

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