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Pollen structure and development in Nymphaeales: Insights into character evolution in an ancient angiosperm lineage

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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.1537-2197.1966.tb06879.xopenalex-snapshot

FINE STRUCTURAL STUDIES OF ZEA MAYS POLLEN I: CELL MEMBRANES AND EXINE ONTOGENY

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.1537-2197.1974.tb12329.xopenalex-snapshot

APERTURE EVOLUTION IN THE POLLEN OF PRIMITIVE ANGIOSPERMS

inferredcites →https://doi.org/10.1002/j.1537-2197.1989.tb15168.xopenalex-snapshot

MORPHOLOGICAL STUDIES OF THE NYMPHAEACEAE SENSU LATO. XVII. FLORAL ANATOMY OF ONDINEA PURPUREA SUBSPECIES PURPUREA (NYMPHAEACEAE)

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/j.1537-2197.1992.tb13657.xopenalex-snapshot

CYCLIC INVASION OF TAPETAL CELLS INTO LOCULI DURING MICROSPORE DEVELOPMENT IN NYMPHAEA COLORATA (NYMPHACEAE)

inferredcites →https://doi.org/10.1002/j.1537-2197.1995.tb11573.xopenalex-snapshot

P ollen morphology and ultrastructure of the B ennettitales : I n situ pollen of C ycadeoidea

inferredcites →https://doi.org/10.1002/j.1537-2197.1995.tb15645.xopenalex-snapshot

The pollen grain wall as a site for passage of lanthanum in tomato, Lycopersicon esculentum (Solanaceae)

inferredcites →https://doi.org/10.1002/tax.574004openalex-snapshot

Phylogeny and evolutionary patterns in Nymphaeales: integrating genes, genomes and morphology

inferredcites →https://doi.org/10.1002/tax.574008openalex-snapshot

Biogeography of Nymphaeales: extant patterns and historical events

inferredcites →https://doi.org/10.1002/tax.574009openalex-snapshot

Pluricarpellatia , a nymphaealean angiosperm from the Lower Cretaceous of northern Gondwana (Crato Formation, Brazil)

inferredcites →https://doi.org/10.1006/anbo.1999.0942openalex-snapshot

Microsporogenesis in Monocotyledons

inferredcites →https://doi.org/10.1007/978-3-7091-6661-1_2openalex-snapshot

Tapetum development in Cucurbita pepo (Cucurbitaceae)

inferredcites →https://doi.org/10.1007/978-3-7091-6910-0_9openalex-snapshot

Floral aspects of Barclaya (Nymphaeaceae): pollination, ontogeny and structure

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

Sporoderm development inNymphaea mexicana (Nymphaeaceae)

inferredcites →https://doi.org/10.1007/bf01283603openalex-snapshot

�ber das Antherentapetum mit besonderer Ber�cksichtigung seiner Kernzahl

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/bf03052339openalex-snapshot

Morphological and embryological studies in Nymphaeaceae

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/s00606-006-0465-2openalex-snapshot

Exine development: the importance of looking through a colloid chemistry ``window''

inferredcites →https://doi.org/10.1007/s00606-007-0631-1openalex-snapshot

Reproductive morphology of Nuphar (Nymphaeaceae), a member of basal angiosperms

inferredcites →https://doi.org/10.1007/s00606-011-0479-2openalex-snapshot

Exine and tapetum development in Symphytum officinale (Boraginaceae). Exine substructure and its interpretation

inferredcites →https://doi.org/10.1007/s00709-014-0631-2openalex-snapshot

Sporoderm and tapetum development in Eupomatia laurina (Eupomatiaceae). An interpretation

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/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.tplants.2004.01.001openalex-snapshot

Pollen aperture evolution – a crucial factor for eudicot success?

inferredcites →https://doi.org/10.1016/s0034-6667(03)00081-2openalex-snapshot

Sporoderm ontogeny in Cabomba aquatica (Cabombaceae)

inferredcites →https://doi.org/10.1016/s0304-3991(75)80018-0openalex-snapshot

A simple procedure for mounting wrinkle-free sections on formvar-coated slot grids

inferredcites →https://doi.org/10.1017/s0094837300015840openalex-snapshot

Phylogenies and angiosperm diversification

inferredcites →https://doi.org/10.1038/35066557openalex-snapshot

Fossil evidence of water lilies (Nymphaeales) in the Early Cretaceous

inferredcites →https://doi.org/10.1038/46536openalex-snapshot

The earliest angiosperms: evidence from mitochondrial, plastid and nuclear genomes

inferredcites →https://doi.org/10.1038/nature05612openalex-snapshot

Hydatellaceae identified as a new branch near the base of the angiosperm phylogenetic tree

inferredcites →https://doi.org/10.1046/j.1095-8312.2003.00258.xopenalex-snapshot

Water lilies and scarabs: faithful partners for 100 million years?

inferredcites →https://doi.org/10.1071/bt9830371openalex-snapshot

Gross morphology and floral biology on Ondinea purpurea den Hartog

inferredcites →https://doi.org/10.1073/pnas.0800036105openalex-snapshot

Novelties of the flowering plant pollen tube underlie diversification of a key life history stage

inferredcites →https://doi.org/10.1080/00087114.1976.10796674openalex-snapshot

Tapetal Ultrastructural Changes During Pollen Development. III. Studies onGentiana Acaulis

inferredcites →https://doi.org/10.1080/00173130152591831openalex-snapshot

Re-evaluation of a neglected layer in pollen wall development with comments on its evolution

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/10.1080/00173130802184214openalex-snapshot

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

inferredcites →https://doi.org/10.1080/00173134.2012.673635openalex-snapshot

Tapetum structure and ontogeny inVictoria(Nymphaeaceae)

inferredcites →https://doi.org/10.1080/00173134.2013.769626openalex-snapshot

Aperture evolution in Nymphaeaceae: insights from a micromorphological and ultrastructural investigation

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/10.1080/00173139309428951openalex-snapshot

Pollen morphology of the Amborellaceae and Hortoniaceae (Hortonioideae: Monimiaceae)

inferredcites →https://doi.org/10.1080/01916122.1987.9989315openalex-snapshot

Microchannels in the Pollen Grain Exine

inferredcites →https://doi.org/10.1083/jcb.25.2.407openalex-snapshot

A SIMPLIFIED LEAD CITRATE STAIN FOR USE IN ELECTRON MICROSCOPY

inferredcites →https://doi.org/10.1086/317572openalex-snapshot

Gynoecium Structure and Evolution in Basal Angiosperms

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

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

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

Pollen Characters ofAmborella trichopoda(Amborellaceae): A Reinvestigation

inferredcites →https://doi.org/10.1086/319580openalex-snapshot

The Tapetum in Basal Angiosperms: Early Diversity

inferredcites →https://doi.org/10.1086/321919openalex-snapshot

The Flowers in Extant Basal Angiosperms and Inferences on Ancestral Flowers

inferredcites →https://doi.org/10.1086/337419openalex-snapshot

Pollen Wall Development of Austrobaileya maculata

inferredcites →https://doi.org/10.1086/378656openalex-snapshot

Apertures with Lids: Distribution and Significance of Operculate Pollen in Monocotyledons

inferredcites →https://doi.org/10.1086/513476openalex-snapshot

Phylogeny ofNymphaea(Nymphaeaceae): Evidence from Substitutions and Microstructural Changes in the ChloroplasttrnT‐trnFRegion

inferredcites →https://doi.org/10.1086/518839openalex-snapshot

Pollen Ontogeny inEphedra americana(Gnetales)

inferredcites →https://doi.org/10.1086/597269openalex-snapshot

Consequences of Pollination Syndrome Evolution for Postpollination Biology in an Ancient Angiosperm Family

inferredcites →https://doi.org/10.1086/605120openalex-snapshot

Monetianthus mirusgen. et sp. nov., a Nymphaealean Flower from the Early Cretaceous of Portugal

inferredcites →https://doi.org/10.1086/654848openalex-snapshot

Pollen Evolution in the Early‐Divergent Monocot Order Alismatales

inferredcites →https://doi.org/10.1086/661633openalex-snapshot

Comparative Structure and Development of Pollen and Tapetum in Malpighiales, With a Focus on the Parietal Clade

inferredcites →https://doi.org/10.1086/665822openalex-snapshot

Pollen Tube Growth Rates and the Diversification of Flowering Plant Reproductive Cycles

inferredcites →https://doi.org/10.1086/671804openalex-snapshot

Evolution of Pollen and Tapetal Characters in Ochnaceae (Malpighiales)

inferredcites →https://doi.org/10.1086/673246openalex-snapshot

Pollen Ontogeny inVictoria(Nymphaeales)

inferredcites →https://doi.org/10.1086/675935openalex-snapshot

Integrating Early Cretaceous Fossils into the Phylogeny of Living Angiosperms: ANITA Lines and Relatives of Chloranthaceae

inferredcites →https://doi.org/10.1093/aob/mci174openalex-snapshot

Carpels in Brasenia (Cabombaceae) are Completely Ascidiate Despite a Long Stigmatic Crest

inferredcites →https://doi.org/10.1093/aob/mcm011openalex-snapshot

Pollen, Tapetum and Orbicule Development in Modiolastrum malvifolium (Malvaceae)

inferredcites →https://doi.org/10.1093/aob/mcq198openalex-snapshot

Reproductive ecology of the basal angiosperm Trithuria submersa (Hydatellaceae)

inferredcites →https://doi.org/10.1093/molbev/msi019openalex-snapshot

Molecular Evolution and Phylogenetic Utility of the petD Group II Intron: A Case Study in Basal Angiosperms

inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a087136openalex-snapshot

Development of Tapet urn and Microspores in Canna L.: an Example of an Invasive but Non-syncytial Tapetum

inferredcites →https://doi.org/10.1093/sysbio/syt108openalex-snapshot

Another Look at the Root of the Angiosperms Reveals a Familiar Tale

inferredcites →https://doi.org/10.1098/rstb.1996.0110openalex-snapshot

The comparative biology of pollination and mating in flowering plants

inferredcites →https://doi.org/10.1111/j.0107-055x.2007.00140.xopenalex-snapshot

Morphological variation of Nymphaea (Nymphaeaceae) in European Russia

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.1095-8339.2012.01241.xopenalex-snapshot

Evolution and phylogenetic significance of pollen in Annonaceae

inferredcites →https://doi.org/10.1111/j.1438-8677.1975.tb01039.xopenalex-snapshot

A NOTE ON THE POLLINATION OF NOCTURNALLY FLOWERING SPECIES OF NYMPHAEA

inferredcites →https://doi.org/10.1111/j.1442-1984.1987.tb00037.xopenalex-snapshot

The Life History of Euryale ferox Salisb. in Southwestern Japan with Special Reference to Reproductive Ecology

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.1756-1051.1991.tb01819.xopenalex-snapshot

The genus Cabomba (Cabombaceae)–a taxonomic study

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.1756-1051.2001.tb00806.xopenalex-snapshot

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

inferredcites →https://doi.org/10.1134/s1062360414040031openalex-snapshot

Role of genetic control and self-assembly in gametophyte sporoderm ontogeny: Hypotheses and experiment

inferredcites →https://doi.org/10.1139/b03-095openalex-snapshot

Transfer of material through the microspore exine from the loculus into the cytoplasm

inferredcites →https://doi.org/10.1146/annurev.ecolsys.29.1.567openalex-snapshot

PHYLOGENY OF VASCULAR PLANTS

inferredcites →https://doi.org/10.1146/annurev.es.09.110178.002053openalex-snapshot

Origin of Angiosperms

inferredcites →https://doi.org/10.2175/193864700784546945openalex-snapshot

A MANAGER'S GUIDE to INTERPRETING ANALYTICAL DATA

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

The Bases of Angiosperm Phylogeny: Palynology

inferredcites →https://doi.org/10.2307/2399366openalex-snapshot

Morphological Studies of the Nymphaeaceae Sensu Lato. XVI. The Floral Biology of Brasenia Schreberi

inferredcites →https://doi.org/10.2307/2399899openalex-snapshot

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

inferredcites →https://doi.org/10.2307/25065680openalex-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/10.3372/wi.39.39104openalex-snapshot

The unusualOndinea, actually just another Australian water-lily ofNymphaeasubg.Anecphya (Nymphaeaceae)

inferredcites →https://doi.org/10.3732/ajb.0800016openalex-snapshot

Pollination biology of basal angiosperms (ANITA grade)

inferredcites →https://doi.org/10.3732/ajb.0800070openalex-snapshot

Amborella trichopoda (Amborellaceae) and the evolutionary developmental origins of the angiosperm progamic phase

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

Pollen ontogeny in Brasenia (Cabombaceae, Nymphaeales)

inferredcites →https://doi.org/10.3732/ajb.94.7.1073openalex-snapshot

Morphology of Hydatellaceae, an anomalous aquatic family recently recognized as an early‐divergent angiosperm lineage

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/10.3732/ajb.95.4.399openalex-snapshot

Pollen and anther ontogeny in Cabomba caroliniana (Cabombaceae, Nymphaeales)

inferredcites →https://doi.org/10.7751/telopea20116014openalex-snapshot

Towards a complete species tree of Nymphaea: shedding further light on subg. Brachyceras and its relationships to the Australian water-lilies

What points at this work

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

inferred← citeshttps://doi.org/10.37520/fi.2022.016zenodo-depositor-declared

The Early Cretaceous mesofossil flora of Catefica, Portugal: angiosperms

inferred← citeshttps://doi.org/10.1007/s00425-017-2702-zopenalex-snapshot

Self-assembly as the underlying mechanism for exine development in Larix decidua D. C.

inferred← citeshttps://doi.org/10.1007/s00425-025-04852-5openalex-snapshot

The influence of anther locular fluid on exine self-assembly, investigated by in vivo transplantation experiments

inferred← citeshttps://doi.org/10.1007/s00606-016-1322-6openalex-snapshot

Simulation of exine patterns by self-assembly

inferred← citeshttps://doi.org/10.1007/s00606-019-01610-5openalex-snapshot

Why the monophyly of Nymphaeaceae currently remains indeterminate: an assessment based on gene-wise plastid phylogenomics

inferred← citeshttps://doi.org/10.1007/s00709-016-1074-8openalex-snapshot

Developmental and ultrastructural characters of the pollen grains and tapetum in species of Nymphaea subgenus Hydrocallis

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/s00709-018-1320-3openalex-snapshot

Suggested mechanisms underlying pollen wall development in Ambrosia trifida (Asteraceae: Heliantheae)

inferred← citeshttps://doi.org/10.1007/s00709-022-01777-8openalex-snapshot

Pollen wall and tapetal development in Cymbalaria muralis: the role of physical processes, evidenced by in vitro modelling

inferred← citeshttps://doi.org/10.1007/s00709-024-01970-xopenalex-snapshot

Mechanisms of pollen wall development in Lysimachia vulgaris

inferred← citeshttps://doi.org/10.1007/s10265-016-0862-8openalex-snapshot

Comparative exine development from the post-tetrad stage in the early-divergent lineages of Ranunculales: the genera Euptelea and Pteridophyllum

inferred← citeshttps://doi.org/10.1016/j.aquabot.2020.103267openalex-snapshot

Nymphaea pulchella (Nymphaeaceae) and Trigona spinipes (Apidae) interaction: From florivory to effective pollination in ponds surrounded by pasture

inferred← citeshttps://doi.org/10.1016/j.revpalbo.2021.104413openalex-snapshot

Pollen development in three selected species of Rubiaceae provides ontogenetic evidence for pollen evolution

inferred← citeshttps://doi.org/10.1016/j.scienta.2021.110268openalex-snapshot

Flowering characteristics and reproductive biology of Nymphaea hybrid, a precious water lily

inferred← citeshttps://doi.org/10.1080/00173134.2024.2375209openalex-snapshot

Qualitative LM and SEM study of the Messel palynoflora: part I. Algae to Vitales

inferred← citeshttps://doi.org/10.1080/01916122.2017.1288035openalex-snapshot

The fossil pollen tetrad Quadripollis krempii Drugg 1967; morphology, palaeogeography and botanical affinity

inferred← citeshttps://doi.org/10.1093/aob/mcz027openalex-snapshot

Mimicking pollen and spore walls: self-assembly in action

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/10.1111/njb.03392openalex-snapshot

A reassessment of the genus Barclaya (Nymphaeaceae) including three new species

inferred← citeshttps://doi.org/10.1111/nph.16318openalex-snapshot

Artificial pollen walls simulated by the tandem processes of phase separation and self‐assemblyin vitro

inferred← citeshttps://doi.org/10.1111/pce.13089openalex-snapshot

Sensitivity of sorghum pollen and pistil to high‐temperature stress

inferred← citeshttps://doi.org/10.1111/plb.12850openalex-snapshot

Disentangling historical signal and pollinator selection on the micromorphology of flowers: an example from the floral epidermis of the Nymphaeaceae

inferred← citeshttps://doi.org/10.1111/tpj.15070openalex-snapshot

An integral insight into pollen wall development: involvement of physical processes in exine ontogeny inCalycanthus floridusL., with an experimental approach

inferred← citeshttps://doi.org/10.1134/s0031030119020126openalex-snapshot

Further Interpretation of Wodehouseia spinata Stanley from the Late Maastrichtian of the Far East (China)

inferred← citeshttps://doi.org/10.1134/s1062360423050053openalex-snapshot

The Role of Physical Processes in Pollen Wall Morphogenesis: Hypothesis and Experimental Confirmation

inferred← citeshttps://doi.org/10.1590/0001-3765202020181382openalex-snapshot

Pollen and microsporangium development in Ziziphus jujuba, Z. mucronata, Paliurus spina-christi and Gouania ulmifolia (Rhamnaceae)

inferred← citeshttps://doi.org/10.1590/2236-8906e342024openalex-snapshot

Flora Polínica da Reserva do Parque Estadual das Fontes do Ipiranga (São Paulo, Brasil). Famílias: 12A-Cabombaceae e 12-Nymphaeaceae

inferred← citeshttps://doi.org/10.17129/botsci.2696openalex-snapshot

Pollen morphology of the Megamexican cycads reveals the potential of morphometrics to identify cycad genera

inferred← citeshttps://doi.org/10.20944/preprints201905.0002.v1openalex-snapshot

Why the Monophyly of Nymphaeaceae Currently Remains Indeterminate: An Assessment Based on Gene-Wise Plastid Phylogenomics

inferred← citeshttps://doi.org/10.31857/s0475145023050051openalex-snapshot

The Role of Physical Processes in Pollen Wall Morphogenesis: Hypothesis and Experimental Confirmation

inferred← citeshttps://doi.org/10.3390/agronomy12112592openalex-snapshot

Comparative Study on Pollen Viability of Camellia oleifera at Four Ploidy Levels

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Morphology and Viability of Pollen from Three Hardy Water Lilies and Their Cross-Compatibility with Nymphaea hybrid

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