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Pollen Diversity in Some Modern Magnoliids

https://doi.org/10.1086/317573
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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.tb12315.xopenalex-snapshot
EVOLUTION OF EXINE STRUCTURE IN THE POLLEN OF PRIMITIVE ANGIOSPERMS
inferredcites →https://doi.org/10.1002/j.1537-2197.1980.tb07690.xopenalex-snapshot
COMPARATIVE POLLEN MORPHOLOGY OF THE MAINLAND AFRICAN GENERA OF MYRISTICACEAE (CEPHALOSPHAERA, COELOCARYON, PYCNANTHUS, AND SCYPHOCEPHALIUM)
inferredcites →https://doi.org/10.1002/j.1537-2197.1983.tb06398.xopenalex-snapshot
COMPARATIVE POLLEN MORPHOLOGY OF THE AMERICAN MYRISTICACEOUS GENERA OTOBA, IRYANTHERA, AND OSTEOPHLOEUM
inferredcites →https://doi.org/10.1002/j.1537-2197.1987.tb12150.xopenalex-snapshot
FIRST FOSSIL EVIDENCE FOR THE PRIMITIVE ANGIOSPERM FAMILY LACTORIDACEAE
inferredcites →https://doi.org/10.1002/j.1537-2197.1990.tb11396.xopenalex-snapshot
EARLY CRETACEOUS TETRADS, ZONASULCULATE POLLEN, AND WINTERACEAE. II. CLADISTIC ANALYSIS AND IMPLICATIONS
inferredcites →https://doi.org/10.1006/anbo.1999.0947openalex-snapshot
Evidence for Stigmatic Self-incompatibility, Pollination Induced Ovule Enlargement and Transmitting Tissue Exudates in the Paleoherb, Saururus cernuus L. (Saururaceae)
inferredcites →https://doi.org/10.1006/bojl.2000.0380openalex-snapshot
Angiosperm phylogeny inferred from 18S rDNA, rbcL, and atpB sequences
inferredcites →https://doi.org/10.1007/978-0-585-23095-5_5openalex-snapshot
Evidence for the Earliest Stage of Angiosperm Pollen Evolution: A Paleoequatorial Section from Israel
inferredcites →https://doi.org/10.1007/bf00936007openalex-snapshot
Pollen evolution and systematics inAnnonaceae with special reference to the disulcate Australian endemic genera
inferredcites →https://doi.org/10.1007/bf00936141openalex-snapshot
Different origins of fragile exines within theAnnonaceae
inferredcites →https://doi.org/10.1007/bf00937294openalex-snapshot
Aperture types withinSapranthus andPolyalthia (Annonaceae)
inferredcites →https://doi.org/10.1007/bf00982528openalex-snapshot
Sporoderm development inNymphaea mexicana (Nymphaeaceae)
inferredcites →https://doi.org/10.1007/bf00984866openalex-snapshot
Pollen morphology ofLactoridaceae
inferredcites →https://doi.org/10.1007/bf00985739openalex-snapshot
Fossil pollen records of the problematical primitive angiosperm familyLactoridaceae in Australia
inferredcites →https://doi.org/10.1007/bf00985928openalex-snapshot
Pollen ultrastructure and systematic affinities ofAnaxagorea (Annonaceae)
inferredcites →https://doi.org/10.1007/bf00987945openalex-snapshot
Significance of palynology for phylogeny ofAnnonaceae: Experiments with removal of pollen characters
inferredcites →https://doi.org/10.1007/bf00989009openalex-snapshot
The sporoderm ultrastructure inPersea, Nectandra, Hernandia, Gomortega and some other Lauralean genera
inferredcites →https://doi.org/10.1007/bf00989392openalex-snapshot
Sporoderm characters ofTetrameranthus duckei (Annonaceae) and their systematic implications
inferredcites →https://doi.org/10.1007/bf00989416openalex-snapshot
Orbicules and the ektexine are homologous sporopollenin concretions inSpermatophyta
inferredcites →https://doi.org/10.1007/bf00989431openalex-snapshot
Systematic relationships of theLactoridaceae, an endemic family of the Juan Fernandez Islands, Chile
inferredcites →https://doi.org/10.1007/bf02344345openalex-snapshot
Development of structure-less pollen wall inCeratophyllum demersum L. (Ceratophyllaceae)
inferredcites →https://doi.org/10.1007/bf02344358openalex-snapshot
Embryology and relationships ofGyrocarpus andHernandia (Hernandiaceae)
inferredcites →https://doi.org/10.1016/0034-6667(92)90023-aopenalex-snapshot
Development of spinous exine in Nuphar japonicum De Candolle (Nymphaeaceae)
inferredcites →https://doi.org/10.1016/0034-6667(94)00083-vopenalex-snapshot
Are the endexines of pteridophytes, gymnosperms and angiosperms structurally equivalent?
inferredcites →https://doi.org/10.1016/0034-6667(94)90057-4openalex-snapshot
Pollen ultrastructure and relationships of Fusaea (Baillon) Safford and Duguetia A. Saint-Hilaire (Annonaceae)
inferredcites →https://doi.org/10.1016/s0016-6995(89)80095-6openalex-snapshot
Pollen and spores form and function
inferredcites →https://doi.org/10.1016/s0254-6299(16)31366-7openalex-snapshot
Dahlgrenodendron, a remarkable new genus of Lauraceae from Natal and Pondoland
inferredcites →https://doi.org/10.1038/46528openalex-snapshot
Angiosperm phylogeny inferred from multiple genes as a tool for comparative biology
inferredcites →https://doi.org/10.1038/46536openalex-snapshot
The earliest angiosperms: evidence from mitochondrial, plastid and nuclear genomes
inferredcites →https://doi.org/10.1071/bt9820297openalex-snapshot
The fine structure of the pollen of Eupomatiaceae
inferredcites →https://doi.org/10.1071/bt9840605openalex-snapshot
Gametogenesis in Galbulimima belgraveana (Himantandraceae)
inferredcites →https://doi.org/10.1080/00173134.1975.11864631openalex-snapshot
Aperture Orientation in Laurelia Pollen (Atherospermataceae Syn. Subfamily Atherospermoideae of Monimiaceae)
inferredcites →https://doi.org/10.1080/00173134.1977.11864640openalex-snapshot
Pollen Tetrads ofHedycarya arboreaJ. R. et G. Forst. (Monimiaceae)
inferredcites →https://doi.org/10.1080/00173136309429108openalex-snapshot
Über Die MöGliche Phylogenetische Bedeutung Der Pollenmorphologie Der MadagassischenBubbia PerrieriR. Cap. (Wintera Ceae)
inferredcites →https://doi.org/10.1080/00173137109427410openalex-snapshot
The Detailed Structure and Ultrastructure of an Acalymmate Tetrad
inferredcites →https://doi.org/10.1080/00173137109427411openalex-snapshot
Contributions to the Pollen Morphology and Phylogeny of the Annonaceae. I
inferredcites →https://doi.org/10.1080/00173137409434768openalex-snapshot
A New Pollen Type in the Winteraceae
inferredcites →https://doi.org/10.1080/00173138009425001openalex-snapshot
The Pollen of the Austrobaileyaceae and its Phylogenetic Significance
inferredcites →https://doi.org/10.1080/00173138109436731openalex-snapshot
Comparative Pollen Morphology of the Madagascan Genera of Myristicaceae (Mauloutchia, Brochoneura, andHaematodendron)
inferredcites →https://doi.org/10.1080/00173138109436732openalex-snapshot
Synchronous versus Asynchronous Mitosis within Permanent Pollen Tetrads of the Winteraceae
inferredcites →https://doi.org/10.1080/00173138409427708openalex-snapshot
Pollen morphology in the trimeniaceae
inferredcites →https://doi.org/10.1080/00173138709428914openalex-snapshot
Developmental Evidence for the Convergence ofSassafras(Laurales) andHeliconia(Zingiberales) Pollen
inferredcites →https://doi.org/10.1080/00173138709428919openalex-snapshot
Short Communications
inferredcites →https://doi.org/10.1080/00173138709429942openalex-snapshot
Pollen morphology ofPalmeria scandensandWilkiea huegeliana(Monimiaceae)
inferredcites →https://doi.org/10.1080/00173138809427729openalex-snapshot
Pollen morphology ofatherosperma, daphnandraanddoryphora(atherospermataceae [monimiaceae])
inferredcites →https://doi.org/10.1080/00173139009427751openalex-snapshot
Pollen types in the lauraceae
inferredcites →https://doi.org/10.1080/00173139009427752openalex-snapshot
Pollen morphology ofpeumus boldus(monimiaceae) — a comparison withpalmeria scandens
inferredcites →https://doi.org/10.1080/00173139309428951openalex-snapshot
Pollen morphology of the Amborellaceae and Hortoniaceae (Hortonioideae: Monimiaceae)
inferredcites →https://doi.org/10.1080/00173139309428979openalex-snapshot
Exine Development, Structure, and Resistance in Pollen of Cinnamomum (Lauraceae)
inferredcites →https://doi.org/10.1080/00173139409429017openalex-snapshot
Exine Development inIllicium ReligiosumSieb. et Zucc. (Illiciaceae)
inferredcites →https://doi.org/10.1080/00173139509430000openalex-snapshot
Pollen morphology of Lactoridaceae — a re-examination
inferredcites →https://doi.org/10.1080/00173139609429081openalex-snapshot
Pollen Morphology and Ultrastructure ofLaurelia, LaureliopsisandDryadodaphne(Atherospermataceae [Monimiaceae])
inferredcites →https://doi.org/10.1080/00173139709362601openalex-snapshot
Pollen morphology and ultrastructure of Australian Monimiaceae ‐Austromatthaea, Hedycarya, Kibara, Leviera, StegantheraandTetrasynandra
inferredcites →https://doi.org/10.1080/00378941.1975.10835640openalex-snapshot
Ultrastructure d'un pollen original parmi les Annonacées(Ambavia)
inferredcites →https://doi.org/10.1080/12538078.1994.10515148openalex-snapshot
Cladistic analysis and pollen evolution inAnnonaceae
inferredcites →https://doi.org/10.1086/336269openalex-snapshot
Comparative Morphology of the Canellaceae. III. Pollen
inferredcites →https://doi.org/10.1086/337419openalex-snapshot
Pollen Wall Development of Austrobaileya maculata
inferredcites →https://doi.org/10.1086/337567openalex-snapshot
Microsporogenesis in a Parthenogenetic Species, Houttuynia cordata Thunb. (Saururaceae)
inferredcites →https://doi.org/10.1111/j.1095-8339.1972.tb00931.xopenalex-snapshot
Contributions to the pollen morphology and phylogeny of the Annonaceae. II
inferredcites →https://doi.org/10.1111/j.1438-8677.1995.tb00498.xopenalex-snapshot
Atomic Force Microscope Information on Pollen Exine Substructure in Nuphar
inferredcites →https://doi.org/10.1111/j.1756-1051.1994.tb01085.xopenalex-snapshot
Exine development in Nymphaea colorata (Nymphaeaceae)
inferredcites →https://doi.org/10.1111/j.1756-1051.1996.tb00239.xopenalex-snapshot
Sporoderm development in Liriodendron chinense (Magnoliaceae): a probable role of the endoplasmic reticulum
inferredcites →https://doi.org/10.1126/science.187.4175.445openalex-snapshot
Primitively Columellaless Pollen: A New Concept in the Evolutionary Morphology of Angiosperms
inferredcites →https://doi.org/10.1126/science.286.5441.947openalex-snapshot
The Root of Angiosperm Phylogeny Inferred from Duplicate Phytochrome Genes
inferredcites →https://doi.org/10.1139/b94-047openalex-snapshot
Pollen development in Liriodendron tulipifera: some unusual features
inferredcites →https://doi.org/10.2307/1221106openalex-snapshot
VARIATION DE LA REGION APERTURALE DANS LE POLLEN DES ANNONACEES
inferredcites →https://doi.org/10.2307/2395271openalex-snapshot
The Bases of Angiosperm Phylogeny: Palynology
inferredcites →https://doi.org/10.2307/2398916openalex-snapshot
Comparative Pollen Morphology of the American Myristicaceous Genera Compsoneura and Virola
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/10.2307/2399848openalex-snapshot
Molecular Phylogenetics of the Magnoliidae: Cladistic Analyses of Nucleotide Sequences of the Plastid Gene rbcL
inferredcites →https://doi.org/10.2307/2656778openalex-snapshot
Circumscription and phylogeny of the Laurales: evidence from molecular and morphological data
inferredcites →https://doi.org/10.2307/2666196openalex-snapshot
The Pollen of Takhtajania perrieri (Winteraceae)
inferredcites →https://doi.org/10.2307/2992003openalex-snapshot
A Combined Cladistic Analysis of Angiosperms Using rbcL and Non-Molecular Data Sets
inferredcites →https://doi.org/10.2307/2992015openalex-snapshot
An Ordinal Classification for the Families of Flowering Plants
inferredcites →https://doi.org/10.2307/4117134openalex-snapshot
The Evolutionary Significance of the Exine
inferredcites →https://doi.org/10.5642/aliso.19640504.03openalex-snapshot
Morphology and Relationships of Lactoridaceae
inferredcites →https://doi.org/10.5962/p.185600openalex-snapshot
Further Contributions to the Morphology of the Degeneriaceae
inferredcites →https://doi.org/10.5962/p.185698openalex-snapshot
Pollen of Degeneria vitiensis
inferredcites →https://doi.org/10.5962/p.297052openalex-snapshot
De la structure grenue à la structure columellaire dans le pollen des Annonacées
inferredcites →https://doi.org/10.5962/p.297080openalex-snapshot
Le pollen de Bubbia perrieri R. Cap. Rapports palynologiques avec les autres genres de Wintéracées

What points at this work

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

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Microsporogenesis and systematics of Aristolochiaceae
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Class Magnoliopsida (Dicotyledons)
inferred← citeshttps://doi.org/10.1007/978-3-319-58325-9_5openalex-snapshot
Flowers from the Early Cretaceous
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Flowers from the Early Cretaceous
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Self-assembly as the underlying mechanism for exine development in Larix decidua D. C.
inferred← citeshttps://doi.org/10.1007/s00606-003-0107-xopenalex-snapshot
Triaperturate pollen in the monocotyledons: configurations and conjectures
inferred← citeshttps://doi.org/10.1007/s00606-005-0327-3openalex-snapshot
Phylogeny of Schisandraceae based on morphological data: evidence from modern plants and the fossil record
inferred← citeshttps://doi.org/10.1007/s00606-005-0358-9openalex-snapshot
Ultrastructure and diversity of recent and fossil zona-aperturate pollen grains
inferred← citeshttps://doi.org/10.1007/s00606-006-0467-0openalex-snapshot
Variation and similarities in pollen features in some basal angiosperms, with some taxonomic implications
inferred← citeshttps://doi.org/10.1007/s00606-006-0495-9openalex-snapshot
The identification of fossil angiosperm pollen and its bearing on the time and place of the origin of angiosperms
inferred← citeshttps://doi.org/10.1007/s00606-007-0631-1openalex-snapshot
Reproductive morphology of Nuphar (Nymphaeaceae), a member of basal angiosperms
inferred← citeshttps://doi.org/10.1007/s00606-012-0698-1openalex-snapshot
Pollen morphology and ultrastructure of selected species from Annonaceae
inferred← citeshttps://doi.org/10.1007/s00606-016-1322-6openalex-snapshot
Simulation of exine patterns by self-assembly
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/s00709-014-0631-2openalex-snapshot
Sporoderm and tapetum development in Eupomatia laurina (Eupomatiaceae). An interpretation
inferred← citeshttps://doi.org/10.1007/s00709-017-1121-0openalex-snapshot
Pollen wall ontogeny in Polemonium caeruleum (Polemoniaceae) and suggested underlying mechanisms of development
inferred← citeshttps://doi.org/10.1007/s00709-018-1230-4openalex-snapshot
Pollen ultrastructure in Aristolochia manshuriensis and A. contorta (Aristolochiaceae)
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/s10342-010-0465-1openalex-snapshot
Gomortega keule, the neglected and endangered Chilean fruit tree
inferred← citeshttps://doi.org/10.1007/s12549-020-00479-4openalex-snapshot
A myricaceous male inflorescence with pollen in situ from the middle Eocene of Europe
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Callose and its Role in Pollen and Embryo Sac Development in Flowering Plants
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Lovellea wintonensis gen. et sp. nov.- Early Cretaceous (late Albian), anatomically preserved, angiospermous flowers and fruits from the Winton Formation, western Queensland, Australia
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Palynological data on Illiciaceae and Schisandraceae confirm phylogenetic relationships within these two basally-branching angiosperm families
inferred← citeshttps://doi.org/10.1016/j.isci.2020.100913openalex-snapshot
Generalist Pollen-Feeding Beetles During the Mid-Cretaceous
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.revpalbo.2008.01.007openalex-snapshot
Pollen morphology and ultrastructure of selected species of Magnoliaceae
inferred← citeshttps://doi.org/10.1016/j.revpalbo.2008.08.001openalex-snapshot
Evolutionary significance of granular exine structure in the light of phylogenetic analyses
inferred← citeshttps://doi.org/10.1016/j.revpalbo.2008.12.007openalex-snapshot
Comparative pollen morphology and ultrastructure of modern and fossil gnetophytes
inferred← citeshttps://doi.org/10.1016/j.revpalbo.2025.105423openalex-snapshot
The use of transmission electron microscopy when investigating fossil angiosperm pollen: A review and suggestions for future applications
inferred← citeshttps://doi.org/10.1016/s0034-6667(01)00096-3openalex-snapshot
Early Eocene zona-aperturate pollen grains of the Proxapertites type with affinity to Araceae
inferred← citeshttps://doi.org/10.1017/cbo9781139014113.007openalex-snapshot
Pollen evidence for the pollination biology of early flowering plants
inferred← citeshttps://doi.org/10.1038/npg.els.0003696openalex-snapshot
Illiciales
inferred← citeshttps://doi.org/10.1038/npg.els.0003698openalex-snapshot
Amborellales
inferred← citeshttps://doi.org/10.1038/npg.els.0003699openalex-snapshot
Magnoliales
inferred← citeshttps://doi.org/10.1038/s41598-022-08105-3openalex-snapshot
Systematic palynology in Korean Piperales with special focus on its exine surface ornamentation and orbicule morphology
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Phylogenetic analysis of Magnoliales and Myristicaceae based on multiple data sets: implications for character evolution
inferred← citeshttps://doi.org/10.1071/sb04004openalex-snapshot
Structure and relationships of basal relictual angiosperms
inferred← citeshttps://doi.org/10.1073/pnas.0407174101openalex-snapshot
Araceae from the Early Cretaceous of Portugal: Evidence on the emergence of monocotyledons
inferred← citeshttps://doi.org/10.1080/00173130260045431openalex-snapshot
Evolutionary trends in Winteraceae pollen
inferred← citeshttps://doi.org/10.1080/00173130500424557openalex-snapshot
Early evolution of angiosperm pollen as inferred from molecular and morphological phylogenetic analyses
inferred← citeshttps://doi.org/10.1080/00173130701780427openalex-snapshot
Pollen morphology and ultrastructure of Saururaceae
inferred← citeshttps://doi.org/10.1080/00173130802184214openalex-snapshot
Comparative pollen morphology in the early‐divergent angiosperm family Hydatellaceae reveals variation at the infraspecific level
inferred← citeshttps://doi.org/10.1080/00173130802256913openalex-snapshot
Pollen morphology within theMonodoraclade, a diverse group of five African Annonaceae genera
inferred← citeshttps://doi.org/10.1080/00173130903024343openalex-snapshot
Beschorneria yuccoides and Asimina triloba (L.) Dun: Examples for proximal polar germinating pollen in angiosperms
inferred← citeshttps://doi.org/10.1080/00173134.2011.641579openalex-snapshot
Focused ion beam nano-sectioning and imaging: a new method in characterisation of palaeopalynological remains
inferred← citeshttps://doi.org/10.1080/00173134.2012.688863openalex-snapshot
Sporoderm development and substructure inMagnolia sieboldiiand other Magnoliaceae: an interpretation
inferred← citeshttps://doi.org/10.1080/00173134.2013.769626openalex-snapshot
Aperture evolution in Nymphaeaceae: insights from a micromorphological and ultrastructural investigation
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Experimental modelling of exine-like structures
inferred← citeshttps://doi.org/10.1080/00173134.2015.1096302openalex-snapshot
Pollen morphology of selected species from Annonaceae
inferred← citeshttps://doi.org/10.1080/00173134.2017.1365374openalex-snapshot
A contribution to the pollen morphology of the Cryptocarya group (Lauraceae)
inferred← citeshttps://doi.org/10.1080/00173134.2019.1569719openalex-snapshot
Using palynomorphological characteristics for the identification of species of Alsinoideae (Caryophyllaceae): a systematic approach
inferred← citeshttps://doi.org/10.1080/01916122.2017.1298540openalex-snapshot
The morphology and systematics of the pollen of Stellaria
inferred← citeshttps://doi.org/10.1080/01916122.2017.1346527openalex-snapshot
The pollen ofSolanumL. and its systematic significance
inferred← citeshttps://doi.org/10.1080/01916122.2018.1458663openalex-snapshot
Pollen morphology of selected species from the family Solanaceae
inferred← citeshttps://doi.org/10.1080/01916122.2022.2070294openalex-snapshot
Pollen characters and their evolutionary and taxonomic significance: using light and confocal laser scanning microscope to study diverse plant pollen taxa from central India
inferred← citeshttps://doi.org/10.1086/317578openalex-snapshot
Morphological Phylogenetic Analysis of Basal Angiosperms: Comparison and Combination with Molecular Data
inferred← citeshttps://doi.org/10.1086/317579openalex-snapshot
Evolution of Endosperm Developmental Patterns among Basal Flowering Plants
inferred← citeshttps://doi.org/10.1086/317907openalex-snapshot
Pollen Characters ofAmborella trichopoda(Amborellaceae): A Reinvestigation
inferred← citeshttps://doi.org/10.1086/338322openalex-snapshot
Evolution of Microsporogenesis in Angiosperms
inferred← citeshttps://doi.org/10.1086/375424openalex-snapshot
Pollen Diversity and Evolution in Myristicaceae (Magnoliales)
inferred← citeshttps://doi.org/10.1086/378656openalex-snapshot
Apertures with Lids: Distribution and Significance of Operculate Pollen in Monocotyledons
inferred← citeshttps://doi.org/10.1086/380987openalex-snapshot
Morphological Phylogenetic Analysis of Living and Fossil Chloranthaceae
inferred← citeshttps://doi.org/10.1086/423879openalex-snapshot
Endressinia brasiliana, a Magnolialean Angiosperm from the Lower Cretaceous Crato Formation (Brazil)
inferred← citeshttps://doi.org/10.1086/501476openalex-snapshot
Phylogeny and Androecial Evolution in Schisandraceae, Inferred from Sequences of Nuclear Ribosomal DNA ITS and Chloroplast DNAtrnL‐F Regions
inferred← citeshttps://doi.org/10.1086/593045openalex-snapshot
Comparative Gynoecium Structure and Development in Calycanthaceae (Laurales)
inferred← citeshttps://doi.org/10.1086/673246openalex-snapshot
Pollen Ontogeny inVictoria(Nymphaeales)
inferred← citeshttps://doi.org/10.1093/aob/mci030openalex-snapshot
Multiple Developmental Pathways Leading to a Single Morph: Monosulcate Pollen (Examples From the Asparagales)
inferred← citeshttps://doi.org/10.1093/aobpla/pls010openalex-snapshot
The evolution of pollen germination timing in flowering plants: Austrobaileya scandens (Austrobaileyaceae)
inferred← citeshttps://doi.org/10.1093/botlinnean/boaa102openalex-snapshot
Underlying mechanisms of development: pollen wall ontogeny inChloranthus japonicusand a reconsideration of pollen ontogeny in early-diverging lineages of angiosperms
inferred← citeshttps://doi.org/10.1093/jxb/erl128openalex-snapshot
Morphological and molecular phylogenetic context of the angiosperms: contrasting the 'top-down' and 'bottom-up' approaches used to infer the likely characteristics of the first flowers
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2003.tb00257.xopenalex-snapshot
MODULARITY OF THE ANGIOSPERM FEMALE GAMETOPHYTE AND ITS BEARING ON THE EARLY EVOLUTION OF ENDOSPERM IN FLOWERING PLANTS
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2004.00342.xopenalex-snapshot
The exine ultrastructure of pollen grains in Gnetum (Gnetaceae) from China and its bearing on the relationship with the ANITA Group
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2005.00422.xopenalex-snapshot
Fruit structure of Amborella trichopoda (Amborellaceae)
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2007.00694.xopenalex-snapshot
Why does some pollen lack apertures? A review of inaperturate pollen in eudicots
inferred← citeshttps://doi.org/10.1111/j.1744-7909.2009.00838.xopenalex-snapshot
The Earliest Normal Flower from Liaoning Province, China
inferred← citeshttps://doi.org/10.1111/jbi.13154openalex-snapshot
A Winteraceae pollen tetrad from the early Paleocene of western Greenland, and the fossil record of Winteraceae in Laurasia and Gondwana
inferred← citeshttps://doi.org/10.1111/nph.71310openalex-snapshot
Trimerous magnoliid flowers with a unique set of floral and pollen traits from the Late Cretaceous of Southern Bohemia (Czech Republic)
inferred← citeshttps://doi.org/10.1515/abcsb-2017-0007openalex-snapshot
Pollen Morphology of Some Species of the Genus Sansevieria Petagna (Asparagaceae)
inferred← citeshttps://doi.org/10.1515/acpa-2017-0015openalex-snapshot
Pollen morphology of extant Winteraceae: a study allowing SEM-based affiliation of its fossil representatives
inferred← citeshttps://doi.org/10.15517/rbt.v62i3.12051openalex-snapshot
Anatomía y desarrollo de estambres y carpelos en Drimys granadensis (Winteraceae)
inferred← citeshttps://doi.org/10.1663/0006-8101(2007)73[67:aucotc]2.0.co;2openalex-snapshot
An Updated Classification of the Class Magnoliopsida (“Angiospermae”)
inferred← citeshttps://doi.org/10.2307/25065680openalex-snapshot
Reconstructing the basal angiosperm phylogeny: evaluating information content of mitochondrial genes
inferred← citeshttps://doi.org/10.2307/4135484openalex-snapshot
A Transitional-Combinational Theory for the Origin of Angiosperms
inferred← citeshttps://doi.org/10.3159/1095-5674(2006)133[169:sfatoo]2.0.co;2openalex-snapshot
Seed ferns and the origin of angiosperms
inferred← citeshttps://doi.org/10.3390/d14090705openalex-snapshot
Pollen Morphology of Rosa sericea Complex and Their Taxonomic Contribution
inferred← citeshttps://doi.org/10.3417/2012047openalex-snapshot
Evolution of Angiosperm Pollen. 1. Introduction1
inferred← citeshttps://doi.org/10.3417/2012048openalex-snapshot
Evolution of Angiosperm Pollen. 2. The Basal Angiosperms1
inferred← citeshttps://doi.org/10.3417/2014014openalex-snapshot
Evolution of Angiosperm Pollen. 3. Monocots1
inferred← citeshttps://doi.org/10.3732/ajb.0800016openalex-snapshot
Pollination biology of basal angiosperms (ANITA grade)
inferred← citeshttps://doi.org/10.3732/ajb.0800047openalex-snapshot
Reconstructing the ancestral angiosperm flower and its initial specializations
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.1600047openalex-snapshot
Hedycarya macrofossils and associated Planarpollenites pollen from the early Miocene of New Zealand
inferred← citeshttps://doi.org/10.3732/ajb.94.10.1642openalex-snapshot
Establishing a fossil record for the perianthless Piperales: Saururus tuckerae sp. nov. (Saururaceae) from the Middle Eocene Princeton Chert
inferred← citeshttps://doi.org/10.3732/ajb.94.12.2041openalex-snapshot
Potomacanthus lobatus gen. et sp. nov., a new flower of probable Lauraceae from the Early Cretaceous (Early to Middle Albian) of eastern North America
inferred← citeshttps://doi.org/10.3897/phytokeys.38.7495openalex-snapshot
Pantoporate pollen in the Asteraceae (Vernonieae)
inferred← citeshttps://doi.org/10.5091/plecevo.2010.438openalex-snapshot
Distribution of orbicules in Annonaceae mirrors evolutionary trend in angiosperms
inferred← citeshttps://doi.org/10.5281/zenodo.3763334openalex-snapshot
Comparative pollen morphology of Calycanthaceae for their taxonomic implication
inferred← citeshttps://doi.org/10.7287/peerj.3434v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Tiny pollen grains: first evidence of Saururaceae from the Late Cretaceous of western North America (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.3434v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Tiny pollen grains: first evidence of Saururaceae from the Late Cretaceous of western North America (v0.1)"
inferred← citeshttps://doi.org/10.7717/peerj.3434openalex-snapshot
Tiny pollen grains: first evidence of Saururaceae from the Late Cretaceous of western North America
inferred← citeshttps://doi.org/10.7751/telopea20065734openalex-snapshot
Pollen morphology of some rainforest taxa occurring in the Illawarra region of New South Wales, Australia
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