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Evolution of Angiosperm Pollen. 2. The Basal Angiosperms1

https://doi.org/10.3417/2012048

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

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THE USE OF POLLEN MORPHOLOGY IN THE TAXONOMY OF DICENTRA

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EVOLUTION OF EXINE STRUCTURE IN THE POLLEN OF PRIMITIVE ANGIOSPERMS

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COMPARATIVE POLLEN MORPHOLOGY AND TAXONOMIC AFFINITIES IN CYCADALES

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EARLY CRETACEOUS TETRADS, ZONASULCULATE POLLEN, AND WINTERACEAE. I. TAXONOMY, MORPHOLOGY, AND ULTRASTRUCTURE

inferredcites →https://doi.org/10.1002/j.1537-2197.1991.tb12603.xopenalex-snapshot

POLLEN MORPHOLOGY AND ULTRASTRUCTURE OF THE CABOMBACEAE: CORRELATIONS WITH POLLINATION BIOLOGY

inferredcites →https://doi.org/10.1002/jez.10150openalex-snapshot

Aperture pattern ontogeny in angiosperms

inferredcites →https://doi.org/10.1006/bojl.1996.0058openalex-snapshot

Microsporogenesis and microgametogenesis of the Argentinian species ofPodocarpus(Podocarpaceae)

inferredcites →https://doi.org/10.1006/bojl.2000.0380openalex-snapshot

Angiosperm phylogeny inferred from 18S rDNA, rbcL, and atpB sequences

inferredcites →https://doi.org/10.1006/bojl.2001.0478openalex-snapshot

Microsporogenesis and systematics of Aristolochiaceae

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/10.1007/978-3-7091-6306-1_9openalex-snapshot

Abiotic pollen and pollination: ecological, functional, and evolutionary perspectives

inferredcites →https://doi.org/10.1007/978-3-7091-6612-3_7openalex-snapshot

Palynology and systematics of Ranunculiflorae

inferredcites →https://doi.org/10.1007/bf00982528openalex-snapshot

Sporoderm development inNymphaea mexicana (Nymphaeaceae)

inferredcites →https://doi.org/10.1007/bf00983692openalex-snapshot

Pollen grain wall structure ofCaytonanthus arberi (Caytoniales)

inferredcites →https://doi.org/10.1007/bf00984101openalex-snapshot

Abiotic pollen and pollination: Ecological, functional, and evolutionary perspectives

inferredcites →https://doi.org/10.1007/bf00984614openalex-snapshot

The tubular exine ofLauraceae andHernandiaceae, a novel type of exine structure in seed plants

inferredcites →https://doi.org/10.1007/bf00984866openalex-snapshot

Pollen morphology ofLactoridaceae

inferredcites →https://doi.org/10.1007/bf00984923openalex-snapshot

Ripe pollen structure and histochemistry of some gymnosperms

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/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/bf02344345openalex-snapshot

Development of structure-less pollen wall inCeratophyllum demersum L. (Ceratophyllaceae)

inferredcites →https://doi.org/10.1007/bf02861082openalex-snapshot

Seed plant phylogeny and the origin of angiosperms: An experimental cladistic approach

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/s00606-003-0107-xopenalex-snapshot

Triaperturate pollen in the monocotyledons: configurations and conjectures

inferredcites →https://doi.org/10.1007/s00606-005-0358-9openalex-snapshot

Ultrastructure and diversity of recent and fossil zona-aperturate pollen grains

inferredcites →https://doi.org/10.1007/s00606-006-0441-xopenalex-snapshot

The impact of extinct taxa on understanding the early evolution of Angiosperm clades: an example incorporating fossil reproductive structures of Saxifragales

inferredcites →https://doi.org/10.1007/s00606-006-0467-0openalex-snapshot

Variation and similarities in pollen features in some basal angiosperms, with some taxonomic implications

inferredcites →https://doi.org/10.1007/s00606-006-0477-yopenalex-snapshot

Evolution of endoapertures in early-divergent eudicots, with particular reference to pollen morphology in Sabiaceae

inferredcites →https://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

inferredcites →https://doi.org/10.1007/s006060170026openalex-snapshot

Developmental evolution of endosperm in basal angiosperms: evidence from Amborella (Amborellaceae), Nuphar (Nymphaeaceae), and Illicium (Illiciaceae)

inferredcites →https://doi.org/10.1007/s10265-004-0153-7openalex-snapshot

Phylogeny and divergence of basal angiosperms inferred from APETALA3- and PISTILLATA-like MADS-box genes

inferredcites →https://doi.org/10.1016/0034-6667(84)90060-5openalex-snapshot

Berberidaceae

inferredcites →https://doi.org/10.1016/0034-6667(87)90003-0openalex-snapshot

Records of angiospermid pollen entry into the english early cretaceous succession

inferredcites →https://doi.org/10.1016/j.flora.2009.02.004openalex-snapshot

Palynological data on Illiciaceae and Schisandraceae confirm phylogenetic relationships within these two basally-branching angiosperm families

inferredcites →https://doi.org/10.1016/j.palaeo.2005.07.006openalex-snapshot

Cretaceous angiosperm flowers: Innovation and evolution in plant reproduction

inferredcites →https://doi.org/10.1016/j.plantsci.2005.05.006openalex-snapshot

Phylogenetic analysis of the order Nymphaeales based on the nucleotide sequences of the chloroplast ITS2-4 region

inferredcites →https://doi.org/10.1016/j.revpalbo.2004.05.005openalex-snapshot

Exine development in Encephalartos altensteinii (Cycadaceae): ultrastructure, substructure and the modes of sporopollenin accumulation

inferredcites →https://doi.org/10.1016/j.revpalbo.2005.09.006openalex-snapshot

New records of Early Cretaceous angiosperm pollen from Portuguese coastal deposits: Implications for the timing of the early angiosperm radiation

inferredcites →https://doi.org/10.1016/j.revpalbo.2006.06.008openalex-snapshot

Glossary of pollen and spore terminology

inferredcites →https://doi.org/10.1016/j.revpalbo.2008.01.007openalex-snapshot

Pollen morphology and ultrastructure of selected species of Magnoliaceae

inferredcites →https://doi.org/10.1016/j.revpalbo.2008.12.007openalex-snapshot

Comparative pollen morphology and ultrastructure of modern and fossil gnetophytes

inferredcites →https://doi.org/10.1016/j.revpalbo.2008.12.009openalex-snapshot

Pollen morphology of Gaultheria L. and related genera of subfamily Vaccinioideae: Taxonomic and evolutionary significance

inferredcites →https://doi.org/10.1016/j.revpalbo.2009.02.002openalex-snapshot

Occurrence of angiosperm-like ultrastructural features in gymnosperm pollen from the Permian of Russia

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/10.1016/j.tplants.2005.03.006openalex-snapshot

The place of Amborella within the radiation of angiosperms

inferredcites →https://doi.org/10.1016/j.ympev.2006.06.017openalex-snapshot

Phylogenetic utility of rapidly evolving DNA at high taxonomical levels: Contrasting matK, trnT-F, and rbcL in basal angiosperms

inferredcites →https://doi.org/10.1016/j.ympev.2007.06.004openalex-snapshot

Phylogenetic and evolutionary implications of complete chloroplast genome sequences of four early-diverging angiosperms: Buxus (Buxaceae), Chloranthus (Chloranthaceae), Dioscorea (Dioscoreaceae), and Illicium (Schisandraceae)

inferredcites →https://doi.org/10.1016/s0034-6667(02)00153-7openalex-snapshot

ARISTOLOCHIACEAE

inferredcites →https://doi.org/10.1016/s0960-9822(00)80119-0openalex-snapshot

Multigene analyses identify the three earliest lineages of extant flowering plants

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/10.1046/j.1095-8339.2003.00171.xopenalex-snapshot

Phylogenetic analysis of Magnoliales and Myristicaceae based on multiple data sets: implications for character evolution

inferredcites →https://doi.org/10.1071/bt9780265openalex-snapshot

Biology of Australian seagrasses: Pollen development and submarine pollination in Amphibolis antarctica and Thalassodendron ciliatum (Cymodoceaceae)

inferredcites →https://doi.org/10.1071/bt9820297openalex-snapshot

The fine structure of the pollen of Eupomatiaceae

inferredcites →https://doi.org/10.1073/pnas.0708072104openalex-snapshot

Using plastid genome-scale data to resolve enigmatic relationships among basal angiosperms

inferredcites →https://doi.org/10.1073/pnas.0709121104openalex-snapshot

Analysis of 81 genes from 64 plastid genomes resolves relationships in angiosperms and identifies genome-scale evolutionary patterns

inferredcites →https://doi.org/10.1073/pnas.0911223107openalex-snapshot

Foldable structures and the natural design of pollen grains

inferredcites →https://doi.org/10.1073/pnas.092136399openalex-snapshot

The root of the angiosperms revisited

inferredcites →https://doi.org/10.1073/pnas.220427497openalex-snapshot

Independent and combined analyses of sequences from all three genomic compartments converge on the root of flowering plant phylogeny

inferredcites →https://doi.org/10.1078/1433-8319-00052openalex-snapshot

Phylogenetic affinities of Monimiaceae based on cpDNA gene and spacer sequences

inferredcites →https://doi.org/10.1080/00173130052017262openalex-snapshot

Fossil floral structures of a basal angiosperm with monocolpate, reticulate-acolumellate pollen from the Early Cretaceous of Portugal

inferredcites →https://doi.org/10.1080/001731300750044591openalex-snapshot

Morphologie et ultrastructure du pollen des Siparunaceae (Laurales)

inferredcites →https://doi.org/10.1080/00173130152987508openalex-snapshot

Pollen morphology of endemic species of the Horton Plains National Park, Sri Lanka

inferredcites →https://doi.org/10.1080/00173130260045431openalex-snapshot

Evolutionary trends in Winteraceae pollen

inferredcites →https://doi.org/10.1080/00173130310008535openalex-snapshot

Triporate pollen in the Arecaceae

inferredcites →https://doi.org/10.1080/00173130310017625openalex-snapshot

Principal modes of infoldings in tricolp(or)ate Angiosperm pollen

inferredcites →https://doi.org/10.1080/00173130500230459openalex-snapshot

Pollen germination inWelwitschia mirabilisHook. f.: differences between the polyplicate pollen producing genera of the Gnetales

inferredcites →https://doi.org/10.1080/00173130500424557openalex-snapshot

Early evolution of angiosperm pollen as inferred from molecular and morphological phylogenetic analyses

inferredcites →https://doi.org/10.1080/00173130701485191openalex-snapshot

Aperture variation in the pollen ofNelumbo(Nelumbonaceae)

inferredcites →https://doi.org/10.1080/00173130701780427openalex-snapshot

Pollen morphology and ultrastructure of Saururaceae

inferredcites →https://doi.org/10.1080/00173130802184214openalex-snapshot

Comparative pollen morphology in the early‐divergent angiosperm family Hydatellaceae reveals variation at the infraspecific level

inferredcites →https://doi.org/10.1080/00173134.1975.11864626openalex-snapshot

Irregular Pollen Grains in Some Hypericum Species

inferredcites →https://doi.org/10.1080/00173134.2012.688863openalex-snapshot

Sporoderm development and substructure inMagnolia sieboldiiand other Magnoliaceae: an interpretation

inferredcites →https://doi.org/10.1080/00173136609430035openalex-snapshot

The Fine Structure of Some Gymnosperm Pollen Walls

inferredcites →https://doi.org/10.1080/00173137209429874openalex-snapshot

Pollen Morphology of the Family Magnoliaceae

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/10.1080/00173138409427708openalex-snapshot

Pollen morphology in the trimeniaceae

inferredcites →https://doi.org/10.1080/00173138709428919openalex-snapshot

Short Communications

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/10.1080/00173139309429457openalex-snapshot

Polymorphism of pollen in the genus Acer (Aceraceae)

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/10.1080/00173139709362601openalex-snapshot

Pollen morphology and ultrastructure of Australian Monimiaceae ‐Austromatthaea, Hedycarya, Kibara, Leviera, StegantheraandTetrasynandra

inferredcites →https://doi.org/10.1080/10635159950127402openalex-snapshot

Timing Transantarctic Disjunctions in the Atherospermataceae (Laurales): Evidence from Coding and Noncoding Chloroplast Sequences

inferredcites →https://doi.org/10.1080/10635159950173861openalex-snapshot

Phylogenetics of Flowering Plants Based on Combined Analysis of Plastid atpB and rbcL Gene Sequences

inferredcites →https://doi.org/10.1086/297401openalex-snapshot

Seed Plant Phylogeny and the Relationships of Gnetales

inferredcites →https://doi.org/10.1086/297477openalex-snapshot

Systematics of Acorus: Ovule and Anther

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

Pollen Diversity in Some Modern Magnoliids

inferredcites →https://doi.org/10.1086/317577openalex-snapshot

Floral Development of Nelumbo nucifera (Nelumbonaceae)

inferredcites →https://doi.org/10.1086/317578openalex-snapshot

Morphological Phylogenetic Analysis of Basal Angiosperms: Comparison and Combination with Molecular Data

inferredcites →https://doi.org/10.1086/317582openalex-snapshot

Basal Angiosperm Phylogeny Inferred from Duplicate Phytochromes A and C

inferredcites →https://doi.org/10.1086/317584openalex-snapshot

Phylogeny of Basal Angiosperms: Analyses of Five Genes from Three Genomes

inferredcites →https://doi.org/10.1086/317907openalex-snapshot

Pollen Characters ofAmborella trichopoda(Amborellaceae): A Reinvestigation

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/10.1086/375424openalex-snapshot

Pollen Diversity and Evolution in Myristicaceae (Magnoliales)

inferredcites →https://doi.org/10.1086/380987openalex-snapshot

Morphological Phylogenetic Analysis of Living and Fossil Chloranthaceae

inferredcites →https://doi.org/10.1086/431800openalex-snapshot

Phylogenetic Analyses of Basal Angiosperms Based on Nine Plastid, Mitochondrial, and Nuclear Genes

inferredcites →https://doi.org/10.1086/509788openalex-snapshot

A 567‐Taxon Data Set for Angiosperms: The Challenges Posed by Bayesian Analyses of Large Data Sets

inferredcites →https://doi.org/10.1086/593045openalex-snapshot

Comparative Gynoecium Structure and Development in Calycanthaceae (Laurales)

inferredcites →https://doi.org/10.1093/bioinformatics/btl446openalex-snapshot

RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models

inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a088359openalex-snapshot

Germination of Monocolpate Angiosperm Pollen: Evolution of the Actin Cytoskeleton and Wall during Hydration, Activation and Tube Emergence

inferredcites →https://doi.org/10.1093/sysbio/49.2.306openalex-snapshot

Phylogenetics of Flowering Plants Based on Combined Analysis of Plastid atpB and rbcL Gene Sequences

inferredcites →https://doi.org/10.1098/rstb.2009.0228openalex-snapshot

The evolution of floral biology in basal angiosperms

inferredcites →https://doi.org/10.1111/j.1095-8339.1996.tb02072.xopenalex-snapshot

Microsporogenesis and microgametogenesis of the Argentinian species of Podocarpus (Podocarpaceae)

inferredcites →https://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

inferredcites →https://doi.org/10.1111/j.1095-8339.2007.00694.xopenalex-snapshot

Why does some pollen lack apertures? A review of inaperturate pollen in eudicots

inferredcites →https://doi.org/10.1111/j.1095-8339.2009.00996.xopenalex-snapshot

An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III

inferredcites →https://doi.org/10.1111/j.1095-8339.2009.01024.xopenalex-snapshot

Systematic implications of seed coat diversity in Gaultherieae (Ericaceae)

inferredcites →https://doi.org/10.1111/j.1469-185x.1970.tb01649.xopenalex-snapshot

PALYNOLOGICAL EVIDENCE ON EARLY DIFFERENTIATION OF ANGIOSPERMS

inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02060.xopenalex-snapshot

Pollen wall development in flowering plants

inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04212.xopenalex-snapshot

Highly conserved low‐copy nuclear genes as effective markers for phylogenetic analyses in angiosperms

inferredcites →https://doi.org/10.1111/j.1756-1051.2001.tb00806.xopenalex-snapshot

Exine and tapetum development in Nymphaea capensis (Nymphaeaceae): a comparative study

inferredcites →https://doi.org/10.1111/j.1759-6831.2010.00097.xopenalex-snapshot

Angiosperm phylogeny inferred from sequences of four mitochondrial genes

inferredcites →https://doi.org/10.1126/science.172.3983.565openalex-snapshot

Unique Type of Angiosperm Pollen from the Family Annonaceae

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/10.1127/palb/282/2009/69openalex-snapshot

Metasequoia Hu et Cheng (Cupressaceae) from the Eocene of Axel Heiberg Island, Canadian High Arctic

inferredcites →https://doi.org/10.1134/s0031030107110159openalex-snapshot

On some peculiarities of sporoderm structure in members of the Cycadales and Ginkgoales

inferredcites →https://doi.org/10.1155/2010/612017openalex-snapshot

On the Relationship between Pollen Size and Genome Size

inferredcites →https://doi.org/10.1186/1471-2229-9-129openalex-snapshot

Pollen development in Annona cherimola Mill. (Annonaceae). Implications for the evolution of aggregated pollen

inferredcites →https://doi.org/10.1196/annals.1438.005openalex-snapshot

Origin and Early Evolution of Angiosperms

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

The Bases of Angiosperm Phylogeny: Palynology

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/10.2307/2399115openalex-snapshot

Floral Structure, Systematics, and Phylogeny in Trochodendrales

inferredcites →https://doi.org/10.2307/2399117openalex-snapshot

Comparative Pollen Morphology and Its Relationship to Phylogeny of Pollen in the Hamamelidae

inferredcites →https://doi.org/10.2307/2399470openalex-snapshot

A Contribution to the Pollen Morphology of Neotropical Lauraceae

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/10.2307/2399899openalex-snapshot

Integration of Morphological and Ribosomal RNA Data on the Origin of Angiosperms

inferredcites →https://doi.org/10.2307/2399952openalex-snapshot

Angiosperm Phylogeny Inferred from 18S Ribosomal DNA Sequences

inferredcites →https://doi.org/10.2307/25065680openalex-snapshot

Reconstructing the basal angiosperm phylogeny: evaluating information content of mitochondrial genes

inferredcites →https://doi.org/10.2307/2656664openalex-snapshot

Pollen and anther development in Nelumbo (Nelumbonaceae)

inferredcites →https://doi.org/10.2307/2656749openalex-snapshot

Utility of 17 chloroplast genes for inferring the phylogeny of the basal angiosperms

inferredcites →https://doi.org/10.2307/2656778openalex-snapshot

Circumscription and phylogeny of the Laurales: evidence from molecular and morphological data

inferredcites →https://doi.org/10.2307/2666179openalex-snapshot

Early Angiosperm Diversification: The Diversity of Pollen Associated with Angiosperm Reproductive Structures in Early Cretaceous Floras from Portugal

inferredcites →https://doi.org/10.2307/2666196openalex-snapshot

The Pollen of Takhtajania perrieri (Winteraceae)

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/10.2307/2996727openalex-snapshot

Morphology and Anatomy of the Flower and Pollen of Saruma henryi Oliv., a Phylogenetic Relict of the Aristolochiaceae

inferredcites →https://doi.org/10.2307/4110032openalex-snapshot

Pollen Morphology and Taxonomy of the Tribe Menispermeae (Menispermaceae)

inferredcites →https://doi.org/10.3417/2012047openalex-snapshot

Evolution of Angiosperm Pollen. 1. Introduction1

inferredcites →https://doi.org/10.3732/ajb.0800047openalex-snapshot

Reconstructing the ancestral angiosperm flower and its initial specializations

inferredcites →https://doi.org/10.3732/ajb.1000299openalex-snapshot

Evolutionary diversification of the flowers in angiosperms

inferredcites →https://doi.org/10.3732/ajb.1000404openalex-snapshot

Angiosperm phylogeny: 17 genes, 640 taxa

inferredcites →https://doi.org/10.3732/ajb.93.3.344openalex-snapshot

Pollen ontogeny in Brasenia (Cabombaceae, Nymphaeales)

inferredcites →https://doi.org/10.3732/ajb.95.3.340openalex-snapshot

Scutifolium jordanicum gen. et sp. nov. (Cabombaceae), an aquatic fossil plant from the Lower Cretaceous of Jordan, and the relationships of related leaf fossils to living genera

inferredcites →https://doi.org/10.5281/zenodo.16180996openalex-snapshot

Pollen and pollination in the Eupomatiaceae

inferredcites →https://doi.org/10.5479/si.0081024x.50openalex-snapshot

Pollen morphology and the phylogenetic realtionships of the Berberidaceae

inferredcites →https://doi.org/10.5642/aliso.20062201.07openalex-snapshot

Placing the Monocots: Conflicting Signal from Trigenomic Analyses

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The Comparative Morphology of the Winteraceae: I. Pollen and Stamens

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inferredcites →https://doi.org/10.5962/p.297080openalex-snapshot

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inferredcites →https://doi.org/10.5962/p.324625openalex-snapshot

Amborella trichopoda Baill., a New Morphological Type of Vesselless Dicotyledon

inferredcites →https://doi.org/10.5962/p.324720openalex-snapshot

Kadsura heteroclita - Microsporangium and Pollen

inferredcites →https://doi.org/10.5962/p.388395openalex-snapshot

The Developmental Morphology of the Pollen of Proteaceae

What points at this work

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

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inferred← citeshttps://doi.org/10.1016/j.revpalbo.2015.07.009openalex-snapshot

Pollen morphology and post-tetrad wall development in the subfamily Fumarioideae (Papaveraceae)

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/10.1016/j.revpalbo.2018.07.004openalex-snapshot

Morphological and ultrastructural diversity and character evolution of the pollen in the tribe Chelidonieae (Papaveraceae)

inferred← citeshttps://doi.org/10.1021/acs.est.6c05715openalex-snapshot

Integrating Evolutionary Ecology into Urban Aerobiology: Temporal Dynamics and Drivers of Airborne Spore-Pollen Diversity

inferred← citeshttps://doi.org/10.1038/s41467-025-68253-8openalex-snapshot

Pulsed evolution shaped extant angiosperm pollen disparity

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Systematic palynology in Korean Piperales with special focus on its exine surface ornamentation and orbicule morphology

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Palynotaxonomy of Centauropsis (Compositae, Vernonieae) an endemic genus from Madagascar

inferred← citeshttps://doi.org/10.1093/aob/mcaf213openalex-snapshot

Morphological innovation and lineage-specific history drive disparification in the aggregated pollen of mimosoid plants

inferred← citeshttps://doi.org/10.1093/aob/mcy212openalex-snapshot

Evolutionary constraints on disparity of ericaceous pollen grains

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/botlinnean/boae068openalex-snapshot

Evolution of pollen morphology in Calyceraceae and insights into its early evolutionary differentiation

inferred← citeshttps://doi.org/10.1111/nph.70824openalex-snapshot

Climate adaptation and functional constraints drive pollen evolution in Apiales

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/10.1134/s1062359020050088openalex-snapshot

The Structure of Aristolochia tomentosa (Aristolochiaceae) Reproductive Organs

inferred← citeshttps://doi.org/10.1186/s12870-019-2081-7openalex-snapshot

Anatomy and RNA-Seq reveal important gene pathways regulating sex differentiation in a functionally Androdioecious tree, Tapiscia sinensis

inferred← citeshttps://doi.org/10.13057/biodiv/d220347openalex-snapshot

Morphological characteristics of Indonesian Rubus flowers

inferred← citeshttps://doi.org/10.3389/fpls.2016.01991openalex-snapshot

Transcriptome Analysis of Hamelia patens (Rubiaceae) Anthers Reveals Candidate Genes for Tapetum and Pollen Wall Development

inferred← citeshttps://doi.org/10.3417/2012047openalex-snapshot

Evolution of Angiosperm Pollen. 1. Introduction1

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

Evolution of Angiosperm Pollen. 3. Monocots1

inferred← citeshttps://doi.org/10.3417/2015035openalex-snapshot

Evolution of Angiosperm Pollen: 4. Basal Eudicots

inferred← citeshttps://doi.org/10.3417/2017017openalex-snapshot

Evolution of Angiosperm Pollen. 5. Early Diverging Superasteridae (Berberidopsidales, Caryophyllales, Cornales, Ericales, and Santalales) Plus Dilleniales

inferred← citeshttps://doi.org/10.3417/2018074openalex-snapshot

Evolution of Angiosperm Pollen. 6. The Celastrales, Oxalidales, and Malpighiales (Com) Clade and Zygophyllales

inferred← citeshttps://doi.org/10.3417/2019337openalex-snapshot

Evolution of Angiosperm Pollen. 7. Nitrogen-fixing Clade

inferred← citeshttps://doi.org/10.3417/2020500openalex-snapshot

Evolution of Angiosperm Pollen: 8. Lamiids

inferred← citeshttps://doi.org/10.7717/peerj.3434openalex-snapshot

Tiny pollen grains: first evidence of Saururaceae from the Late Cretaceous of western North America

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