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Microsporogenesis and pollen sulcus type in Asparagales (Lilianae)
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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/fedr.19710820202openalex-snapshot
Beiträge zur Pollenmorphologie der Iridaceae und ihre Bedeutung für die Taxonomie
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SPOROGENESIS AND EMBRYO SAC DEVELOPMENT OF HESPEROCALLIS AND LEUCOCRINUM IN RELATION TO THEIR SYSTEMATIC POSITION
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/10.1007/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/bf00951464openalex-snapshot
A radial system of microtubules extending between the nuclear envelope and the plasma membrane during early male haplophase in flowering plants
inferredcites →https://doi.org/10.1007/bf01834936openalex-snapshot
Zur systematischen Stellung vonCyanastrum
inferredcites →https://doi.org/10.1007/bf02344345openalex-snapshot
Development of structure-less pollen wall inCeratophyllum demersum L. (Ceratophyllaceae)
inferredcites →https://doi.org/10.1007/bf03045310openalex-snapshot
A contribution to the embryology of iridaceae
inferredcites →https://doi.org/10.1007/bf03046213openalex-snapshot
Embryological studies inEleutherine plicata Herb. andBelamcanda chinensis Lem
inferredcites →https://doi.org/10.1016/0031-9422(80)85004-7openalex-snapshot
Deviations from michaelis-menten behaviour of plant glutamate dehydrogenase with ammonium as variable substrate
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/10.1016/0034-6667(94)00085-xopenalex-snapshot
Garside's rule and the microspore tetrads of Grevillea rosmarinifolia A. Cunningham and Dryandra polycephala Bentham (Proteaceae)
inferredcites →https://doi.org/10.1016/s0022-5320(69)90033-1openalex-snapshot
A low-viscosity epoxy resin embedding medium for electron microscopy
inferredcites →https://doi.org/10.1016/s0367-1615(17)31274-0openalex-snapshot
Zur vergleichenden Embryologie der Liliaceae-Scilloideae
inferredcites →https://doi.org/10.1071/bt9900433openalex-snapshot
Embryology and Reproductive Ecology of the Darling Lily, Crinum flaccidum Herbert
inferredcites →https://doi.org/10.1073/pnas.90.10.4641openalex-snapshot
Phylogenetic analysis of rbcL sequences identifies Acorus calamus as the primal extant monocotyledon.
inferredcites →https://doi.org/10.1080/00173137209428834openalex-snapshot
The Original Position of the Generative Nucleus in the Pollen Tetrads ofAgropyron, Itea, Limnanthes, and Onosma, and its Phylogenetic Significance in the Angiosperms
inferredcites →https://doi.org/10.1080/00173138509429918openalex-snapshot
Pollen Ultrastructure of the Tecophilaeaceae
inferredcites →https://doi.org/10.1080/00173138709428902openalex-snapshot
Morfología Del Polen De Las Agavaceae Y Algunos Géneros Afines
inferredcites →https://doi.org/10.1080/11035895209453507openalex-snapshot
Pollen Morphology and Plant Taxonomy
inferredcites →https://doi.org/10.1086/335047openalex-snapshot
Morphological Study of Agave lechuguilla
inferredcites →https://doi.org/10.1086/336269openalex-snapshot
Comparative Morphology of the Canellaceae. III. Pollen
inferredcites →https://doi.org/10.1111/j.1096-0031.1996.tb00196.xopenalex-snapshot
PARSIMONY JACKKNIFING OUTPERFORMS NEIGHBOR‐JOINING
inferredcites →https://doi.org/10.1111/j.1756-1051.1985.tb01653.xopenalex-snapshot
Embryology and probable relationships of Eriospermum (Eriospermaceae)
inferredcites →https://doi.org/10.1111/j.1756-1051.1985.tb02067.xopenalex-snapshot
Taxonomic studies of the genus Hypoxis in East Africa
inferredcites →https://doi.org/10.1111/j.1756-1051.1988.tb01701.xopenalex-snapshot
Embryology and possible relationships of Petermannia cirrosa (Petermanniaceae)
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/10.2307/1222713openalex-snapshot
Recognition of the New World Disporum section Prosartes as Prosartes (Liliaceae) based on the sequence data of the rbcL gene
inferredcites →https://doi.org/10.2307/1224136openalex-snapshot
Resurrection of Themidaceae for the Brodiaea alliance, and recircumscription of Alliaceae, Amaryllidaceae and Agapanthoideae
inferredcites →https://doi.org/10.2307/2256877openalex-snapshot
New Zealand Pollen Studies: The Monocotyledons.
inferredcites →https://doi.org/10.2307/2399035openalex-snapshot
Ultrastructure of Lower Cretaceous Angiosperm Pollen and the Origin and Early Evolution of Flowering Plants
inferredcites →https://doi.org/10.2307/2399736openalex-snapshot
Sulcus and Operculum Structure in the Pollen Grains of Iridaceae Subfamily Ixioideae
inferredcites →https://doi.org/10.2307/2399768openalex-snapshot
Monophyly of the Asteridae and Identification of Their Major Lineages Inferred From DNA Sequences of rbcL
inferredcites →https://doi.org/10.2307/2399846openalex-snapshot
Phylogenetics of Seed Plants: An Analysis of Nucleotide Sequences from the Plastid Gene rbcL
inferredcites →https://doi.org/10.2307/2399849openalex-snapshot
Phylogenetic Hypotheses for the Monocotyledons Constructed from rbcL Sequence Data
inferredcites →https://doi.org/10.2307/2412182openalex-snapshot
A Successive Approximations Approach to Character Weighting
inferredcites →https://doi.org/10.2307/2806323openalex-snapshot
Ultrastructural Characters of the Pollen Grains of African Annonaceae and Their Significance for the Phylogeny of Primitive Angiosperms.
inferredcites →https://doi.org/10.2307/4119721openalex-snapshot
New Circumscriptions and a New Family of Asparagoid Lilies: Genera Formerly included in Anthericaceae
inferredcites →https://doi.org/10.2307/4129967openalex-snapshot
Pollen Morphology in Tigridieae (Iridaceae)
inferredcites →https://doi.org/10.5962/p.276348openalex-snapshot
Affinities of the Madagascan endemic Geosiris, Iridaceae or Geosiridaceae
inferredcites →https://doi.org/10.7751/telopea19953017openalex-snapshot
Systematic studies in the eucalypts. 7. A revision of the bloodwoods, genus Corymbia (Myrtaceae)
inferredcites →https://doi.org/10.7751/telopea19963028openalex-snapshot
Systematics of Xanthorrhoeaceae sensu lato: evidence for polyphyly
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Embryology of Polygonatum (Asparagaceae) and its systematic significance
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Pollen morphology and its taxonomic significance in Iranian Colchicum (Colchicaceae)
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Aperture pattern ontogeny in angiosperms
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Iconic, threatened, but largely unknown: Biogeography of the Macaronesian dragon trees (Dracaena spp.) as inferred from plastid DNA markers
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The South American genera of Hemerocallidaceae ( Eccremis and Pasithea ): two introductions to the New World
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Microsporogenesis in Monocotyledons
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Phylogenetics of Asphodelaceae (Asparagales): An Analysis of Plastid rbcL and trnL-F DNA Sequences
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Conservation genetics of an arctic species, Saxifraga rivularis L., in Britain
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Anatomy and morphology of Behnia (Behniaceae) and its relationships within Lilianae: Asparagales
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Angiosperm phylogeny inferred from 18S rDNA, rbcL, and atpB sequences
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Microsporogenesis and systematics of Aristolochiaceae
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Class Liliopsida (Monocotyledons)
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Flowers from the Early Cretaceous
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Flowers from the Early Cretaceous
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Systematic root anatomy of Asparagales and other monocotyledons
inferred← citeshttps://doi.org/10.1007/bf00985358openalex-snapshot
Embryology, cytology and systematics ofHemiphylacus, Asparagus andAnemarrhena (Asparagales)
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The tapetum and systematics in monocotyledons
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Genetic mapping of expressed sequences in onion and in silico comparisons with rice show scant colinearity
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Triaperturate pollen in the monocotyledons: configurations and conjectures
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A phylogenetic analysis of Apostasioideae (Orchidaceae) based on ITS, trnL-F and matK sequences
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Successive microsporogenesis in eudicots, with particular reference to Berberidaceae (Ranunculales)
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Sporogenesis and gametogenesis in Agapanthus praecox Willd. orientalis (Leighton) Leighton and their systematic implications
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Embryology of Iris mandshurica Maxim. (Iridaceae) and its systematic relationships
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Embryology of Hemerocallis L. and its systematic significance
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Postmeiotic cytokinesis and pollen aperture number determination in eudicots: effect of the cleavage wall number
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Links between early pollen development and aperture pattern in monocots
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Molecular phylogeny of monocotyledons inferred from combined analysis of plastid matK and rbcL gene sequences
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The phylogenetic relationships of Asparagales in Korea based on five plastid DNA regions
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Colchicine is still a chemical marker for the expanded Colchicaceae
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Transcriptome landscapes of multiple tissues highlight the genes involved in the flavor metabolic pathway in Chinese chive (Allium tuberosum)
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Phylogeny and biogeographic diversification of Maianthemum (Ruscaceae: Polygonatae)
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Molecular phylogenetics of Hypoxidaceae – Evidence from plastid DNA data and inferences on morphology and biogeography
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Flower and pollen structure of Ruscaceae in relation to Aspidistreae and other Convallariaceae
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Diversification of pollen and tapetum in early-divergent monocots
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Roles of synorganisation, zygomorphy and heterotopy in floral evolution: the gynostemium and labellum of orchids and other lilioid monocots
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Dating the origin of the Orchidaceae from a fossil orchid with its pollinator
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Phylogenetics of Dioscoreales based on combined analyses of morphological and molecular data
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General Comparative Biology of the Monocots
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General Comparative Biology of the Monocots
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General Comparative Biology of the Monocots
inferred← citeshttps://doi.org/10.1071/9780643090149.part07openalex-snapshot
Systematics of the Lilioids
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Systematics of the Lilioids
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The trichotomosulcate asparagoids: pollen morphology of Hemerocallidaceae in relation to systematics and pollination biology
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Structure and systematics of Hanguana , a monocotyledon of uncertain affinity
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Seedling morphology in Iridaceae: Indications for relationships within the family and to related families
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Investigation of mitosis, microsporogenesis and pollen germination in the critically endangered plantAmsonia orientalis(Apocynaceae)
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Spontaneous occurrence of micronuclei in developing microspores ofAgave angustifoliaHaw. cultivar “Lineño” andA. tequilanaWeber cultivar “Azul” (Asparagales, Asparagaceae)
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Pollen and anther characters in monocot systematics
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Pollen aperture morphology in Arecaceae: Application within phylogenetic analyses, and a summary of record of palm-like pollen the fossil
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Triporate pollen in the Arecaceae
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Microsporogenesis is simultaneous in the early‐divergent grass Streptochaeta, but successive in the closest grass relative, Ecdeiocolea
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Microsporogenesis and pollen morphology in dioscoreales and allied taxa
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Comparison of the flora and vegetation of the southern Andes and New Zealand
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Evolution of Microsporogenesis in Angiosperms
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Homologies of Inferior Ovaries and Septal Nectaries in Monocotyledons
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Apertures with Lids: Distribution and Significance of Operculate Pollen in Monocotyledons
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Comparative Pollen Development in Dioscoreales
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Comparative Structure and Development of Pollen and Tapetum in Pandanales
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Evolution of Microsporogenesis in Palms (Arecaceae)
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Pollen Evolution in the Early‐Divergent Monocot Order Alismatales
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Comparative Structure and Development of Pollen and Tapetum in Malpighiales, With a Focus on the Parietal Clade
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Premeiotic Microsporocyte Cell Shape Influences Shape of Tetrads during Microsporogenesis
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Pollen Structure and Diversity in Liliales
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Multiple Developmental Pathways Leading to a Single Morph: Monosulcate Pollen (Examples From the Asparagales)
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The Discovery of Polyandry in Curculigo (Hypoxidaceae): Implications for Androecium Evolution of Asparagoid Monocotyledons
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Molecular phylogenetics of Ruscaceae sensu lato and related families (Asparagales) based on plastid and nuclear DNA sequences
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Genomic data resolve phylogenetic relationships of Australian mat-rushes,Lomandra(Asparagaceae: Lomandroideae)
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A Unique Set of 11,008 Onion Expressed Sequence Tags Reveals Expressed Sequence and Genomic Differences between the Monocot Orders Asparagales and Poales[W]
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Molecular phylogenetic relationships and implications for the circumscription of Colchicaceae (Liliales)
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Familial relationships of the monocot order Liliales based on a molecular phylogenetic analysis using four plastid loci:matK,rbcL,atpBandatpF-H
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Anatomical and molecular systematics of Asteliaceae and Hypoxidaceae
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Systematics of Ruscaceae/Convallariaceae: a combined morphological and molecular investigation
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A subfamilial classification for the expanded asparagalean families Amaryllidaceae, Asparagaceae and Xanthorrhoeaceae
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Molecular Systematics of the Genus Uvularia and Selected Liliales Based upon mat K and rbc L Gene Sequence Data
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Constraints and selection: insights from microsporogenesis in Asparagales
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The Earliest Normal Flower from Liaoning Province, China
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Microsporogenesis of Cycas and its systematic implications
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A palynological study of Dioscorea (Dioscoreaceae) in Korea
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Conserved genome structure and phylogenetic insights for the heterogeneous subfamily of Convallarioideae (Asparagaceae) revealed from plastome data
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Comparative chloroplast genome of six species in Hypoxidaceae from China: insights into phylogenetic relationships and molecular marker development
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Male meiosis and pollen morphology of some populations of Ledebouria revoluta (Asparagaceae) from India
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Alstroemeriaceae en Perú y áreas vecinas
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Anther and pollen development in some species of Poaceae (Poales)
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Parallel Loss of a Slowly Evolving Intron from Two Closely Related Families in Asparagales
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Pollen Evolution in Yams (Dioscorea: Dioscoreaceae)
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Unique Floral Structures and Iterative Evolutionary Themes in Asparagales: Insights from a Morphological Cladistic Analysis
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Systematics and Biology of Silica Bodies in Monocotyledons
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THE NEW PHYLOGENY OF THE LILIOID MONOCOTYLEDONS
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Taxonomic relationships of some taxa of the family Amaryllidaceae (s.l.) as reflected by macro- and micromorphological characters.
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A new classification of Colchicaceae
inferred← citeshttps://doi.org/10.2307/2997255openalex-snapshot
Advances in Angiosperm Systematics: Examples from the Liliales and Asparagales
inferred← citeshttps://doi.org/10.2307/3558433openalex-snapshot
Molecular systematics of Iridaceae: evidence from four plastid DNA regions
inferred← citeshttps://doi.org/10.2307/3668600openalex-snapshot
Flower Anatomy and Systematics of Comospermum (Asparagales)
inferred← citeshttps://doi.org/10.2307/4113631openalex-snapshot
Xeronemataceae, a New Family of Asparagoid Lilies from New Caledonia and New Zealand
inferred← citeshttps://doi.org/10.2307/4117827openalex-snapshot
Two New Monocotyledon Families: Anemarrhenaceae and Behniaceae (Lilianae: Asparagales)
inferred← citeshttps://doi.org/10.2307/4118869openalex-snapshot
Taxonomy of Cyanastroideae (Tecophilaeaceae): A Multidisciplinary Approach
inferred← citeshttps://doi.org/10.2307/4119721openalex-snapshot
New Circumscriptions and a New Family of Asparagoid Lilies: Genera Formerly included in Anthericaceae
inferred← citeshttps://doi.org/10.2478/v10119-009-0011-5openalex-snapshot
The genus Hypoxis L. (Hypoxidaceae) in the East Tropical
inferred← citeshttps://doi.org/10.3329/bjb.v36i2.1498openalex-snapshot
Comparison of pollen morphological structures of some taxa belonging to Asparagus L. and Fritillaria L. (Liliaceae) from Turkey
inferred← citeshttps://doi.org/10.3389/fpls.2020.584981openalex-snapshot
The Deep Evolutionary Relationships of the Morphologically Heterogeneous Nolinoideae (Asparagaceae) Revealed by Transcriptome Data
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/10.3417/2012047openalex-snapshot
Evolution of Angiosperm Pollen. 1. Introduction1
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.1100468openalex-snapshot
Phylogeny of the Asparagales based on three plastid and two mitochondrial genes
inferred← citeshttps://doi.org/10.3732/ajb.90.10.1455openalex-snapshot
Phylogenetic relationships within Colchicaceae
inferred← citeshttps://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
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Multigene Analyses of Monocot Relationships
inferred← citeshttps://doi.org/10.5642/aliso.20062201.15openalex-snapshot
The Operculum in Pollen of Monocotyledons
inferred← citeshttps://doi.org/10.5642/aliso.20062201.16openalex-snapshot
Aperture Pattern and Microsporogenesis in Asparagales
inferred← citeshttps://doi.org/10.5642/aliso.20062201.24openalex-snapshot
Phylogeny, Genome Size, and Chromosome Evolution of Asparagales
inferred← citeshttps://doi.org/10.5642/aliso.20062201.25openalex-snapshot
Genomic Resources for Asparagales
inferred← citeshttps://doi.org/10.5897/jmpr.9000896openalex-snapshot
Microsporogenesis in Rauvolfia serpentina (L.) Benth ex Kurz (Apocynaceae): An evidence for dual cytokinesis in microspore mother cells
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