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Evolution of Angiosperm Pollen. 3. Monocots1

https://doi.org/10.3417/2014014

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

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Beiträge zur Pollenmorphologie der Iridaceae und ihre Bedeutung für die Taxonomie

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THE POLLEN WALL OF CANNA AND ITS SIMILARITY TO THE GERMINAL APERTURES OF OTHER POLLEN

inferredcites →https://doi.org/10.1002/j.1537-2197.1974.tb06048.xopenalex-snapshot

FLORAL DEVELOPMENT OF POTAMOGETON RICHARDSONII

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.1537-2197.1978.tb06172.xopenalex-snapshot

ULTRASTRUCTURE OF EXINE‐LESS POLLEN: HELICONIA (HELICONIACEAE)

inferredcites →https://doi.org/10.1002/j.1537-2197.1981.tb06355.xopenalex-snapshot

ONTOGENETIC AND EVOLUTIONARY IMPLICATIONS OF A NEOTENOUS EXINE IN TAPEINOCHILOS (ZINGIBERALES: COSTACEAE) POLLEN

inferredcites →https://doi.org/10.1002/j.1537-2197.1982.tb13352.xopenalex-snapshot

BEETLE POLLINATION OF CYCLANTHUS BIPARTITUS (CYCLANTHACEAE)

inferredcites →https://doi.org/10.1002/j.1537-2197.1982.tb13363.xopenalex-snapshot

POLLEN MORPHOLOGY IN NORTH AMERICAN SPECIES OF TRILLIUM

inferredcites →https://doi.org/10.1002/j.1537-2197.1982.tb13389.xopenalex-snapshot

MORPHOLOGICAL STUDIES OF THE NYMPHAEACEAE. XII. THE FLORAL BIOLOGY OF CABOMBA CAROLINIANA

inferredcites →https://doi.org/10.1002/j.1537-2197.1983.tb12451.xopenalex-snapshot

THE REPRODUCTIVE BIOLOGY OF A RELICT–ILLICIUM FLORIDANUM ELLIS

inferredcites →https://doi.org/10.1002/j.1537-2197.1987.tb08786.xopenalex-snapshot

DEVELOPMENT OF OMNIAPERTURATE POLLEN IN TRILLIUM KAMTSCHATICUM (LILIACEAE)

inferredcites →https://doi.org/10.1002/j.1537-2197.1989.tb15063.xopenalex-snapshot

POLLEN GRAIN DEVELOPMENT AND TAPETAL CHANGES IN STRELITZIA REGINAE (STRELITZIACEAE)

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/10.1006/bijl.1998.0215openalex-snapshot

Supraspecific taxa as terminals in cladistic analysis: implicit assumptions of monophyly and a comparison of methods

inferredcites →https://doi.org/10.1006/bojl.1999.0253openalex-snapshot

Anatomy and morphology of Behnia (Behniaceae) and its relationships within Lilianae: Asparagales

inferredcites →https://doi.org/10.1006/bojl.2000.0436openalex-snapshot

Morphology of pollen and orbicules in some Dioscorea species and its systematic implications

inferredcites →https://doi.org/10.1007/978-1-4615-6950-3_2openalex-snapshot

A Phylogenetic Classification of the Angiospermae

inferredcites →https://doi.org/10.1007/978-3-642-39417-1openalex-snapshot

Flowering plants, Eudicots : Malpighiales

inferredcites →https://doi.org/10.1007/978-3-642-76395-3openalex-snapshot

Comparative Embryology of Angiosperms

inferredcites →https://doi.org/10.1007/978-3-662-02899-5openalex-snapshot

Flowering Plants · Dicotyledons

inferredcites →https://doi.org/10.1007/978-3-7091-6306-1_1openalex-snapshot

Pollen wall stratification and pollination

inferredcites →https://doi.org/10.1007/978-3-7091-6306-1_12openalex-snapshot

Pollen morphological evolution in bat pollinated plants

inferredcites →https://doi.org/10.1007/978-3-7091-6306-1_5openalex-snapshot

The ecology and evolution of visual pollen signals

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/bf00046049openalex-snapshot

Studies on the reproductive biology of white yam (Dioscorea rotundata Poir.)

inferredcites →https://doi.org/10.1007/bf00230578openalex-snapshot

Composition of the walls of pollen grains of the seagrass Amphibolis antarctica

inferredcites →https://doi.org/10.1007/bf00347603openalex-snapshot

Sunbird pollination of Strelitzia nicolai

inferredcites →https://doi.org/10.1007/bf00936071openalex-snapshot

Self-isolation and insect pollination in the primitive angiosperms: New evaluations of older hypotheses

inferredcites →https://doi.org/10.1007/bf00936141openalex-snapshot

Different origins of fragile exines within theAnnonaceae

inferredcites →https://doi.org/10.1007/bf00936343openalex-snapshot

Pollen morphology of the cypripedioid orchids

inferredcites →https://doi.org/10.1007/bf00937579openalex-snapshot

The remarkable weevil pollination of the neotropicalCarludovicoideae (Cyclanthaceae)

inferredcites →https://doi.org/10.1007/bf00937857openalex-snapshot

Phylogeny of theCyclanthaceae

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

Sporoderm development inNymphaea mexicana (Nymphaeaceae)

inferredcites →https://doi.org/10.1007/bf00983185openalex-snapshot

Bird pollination in South Western Australia: A checklist

inferredcites →https://doi.org/10.1007/bf00984093openalex-snapshot

Pollen wall stratification and pollination

inferredcites →https://doi.org/10.1007/bf00984096openalex-snapshot

The ecology and evolution of pollen odors

inferredcites →https://doi.org/10.1007/bf00984097openalex-snapshot

The ecology and evolution of visual pollen signals

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

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

inferredcites →https://doi.org/10.1007/bf00984104openalex-snapshot

Pollen morphological evolution in bat pollinated plants

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/bf00985240openalex-snapshot

Selfing inNarthecium ossifragum (Melanthiaceae)

inferredcites →https://doi.org/10.1007/bf00989008openalex-snapshot

The fine structure of the pollen wall inStrelitzia reginae (Musaceae)

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/bf01237753openalex-snapshot

Convergence of filiform pollen morphologies in seagrasses: Functional mechanisms

inferredcites →https://doi.org/10.1007/bf01372953openalex-snapshot

Insekten- und Windbest�ubung beiAlisma plantago-aquatica L.

inferredcites →https://doi.org/10.1007/bf02344345openalex-snapshot

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

inferredcites →https://doi.org/10.1007/bf02488182openalex-snapshot

Pollen morphology in Asiatic species ofTrillium

inferredcites →https://doi.org/10.1007/bf02858611openalex-snapshot

Classification and geography of the flowering plants

inferredcites →https://doi.org/10.1007/bf02860996openalex-snapshot

A review of pollination studies in the Palmae

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/bf02869922openalex-snapshot

Evolution of pollen grains

inferredcites →https://doi.org/10.1007/s00239-003-2564-9openalex-snapshot

Dating the Monocot?Dicot Divergence and the Origin of Core Eudicots Using Whole Chloroplast Genomes

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

Partially hydrated pollen: taxonomic distribution, ecological and evolutionary significance

inferredcites →https://doi.org/10.1007/s00606-003-0085-zopenalex-snapshot

Generic relationships among the baccate-fruited Amaryllidaceae (tribe Haemantheae) inferred from plastid and nuclear non-coding DNA sequences

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/s00606-006-0424-yopenalex-snapshot

The systematic value of pollen morphology in Smilacaceae

inferredcites →https://doi.org/10.1007/s00606-008-0111-2openalex-snapshot

Palynological diversity and major evolutionary trends in Cyperaceae

inferredcites →https://doi.org/10.1007/s006060170039openalex-snapshot

Development of the exineless pollen wall in Callitriche truncata (Callitrichaceae) and the evolution of underwater pollination

inferredcites →https://doi.org/10.1007/s006060200023openalex-snapshot

The correlation between development of atypical bisexual flowers and phylogeny in the Aroideae (Araceae)

inferredcites →https://doi.org/10.1007/s10265-003-0133-3openalex-snapshot

Molecular phylogeny of monocotyledons inferred from combined analysis of plastid matK and rbcL gene sequences

inferredcites →https://doi.org/10.1007/s10265-004-0155-5openalex-snapshot

Correlation between pollen morphology and pollination mechanisms in the Hydrocharitaceae

inferredcites →https://doi.org/10.1007/s10682-008-9259-zopenalex-snapshot

Associations between floral specialization and species diversity: cause, effect, or correlation?

inferredcites →https://doi.org/10.1007/s12229-012-9110-7openalex-snapshot

Pollen Morphology of Xyridaceae Systematic (Poales) and its Potential

inferredcites →https://doi.org/10.1016/0034-6667(72)90044-9openalex-snapshot

Pollen morphology of the palmae and its bearing on taxonomy

inferredcites →https://doi.org/10.1016/0034-6667(81)90080-4openalex-snapshot

Alismataceae

inferredcites →https://doi.org/10.1016/0034-6667(88)90044-9openalex-snapshot

Eriocaulaceae

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/10.1016/0047-7206(74)90023-5openalex-snapshot

Pollen in hydrophilous angiosperms

inferredcites →https://doi.org/10.1016/0047-7206(76)90013-3openalex-snapshot

Pollen wall and stigma surface in the marine angiosperms Thalassia and Thalassodendron

inferredcites →https://doi.org/10.1016/0361-9230(90)90257-zopenalex-snapshot

Single unit response of neurons within the hamster suprachiasmatic nucleus to GABA and low chloride perfusate during the day and night

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.pnsc.2008.09.008openalex-snapshot

Phylogenetic studies of the core Alismatales inferred from morphology and rbcL sequences

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.2008.08.001openalex-snapshot

Evolutionary significance of granular exine structure in the light of phylogenetic analyses

inferredcites →https://doi.org/10.1016/j.revpalbo.2008.12.008openalex-snapshot

Comparative pollen morphology and taxonomic considerations in Eriocaulaceae

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

Developmental bases for key innovations in the seed-plant microgametophyte

inferredcites →https://doi.org/10.1016/j.ympev.2009.03.017openalex-snapshot

Repeated evolution of closed fruiting bodies is linked to ascoma development in the largest group of lichenized fungi (Lecanoromycetes, Ascomycota)

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

ARISTOLOCHIACEAE

inferredcites →https://doi.org/10.1016/s0034-6667(97)00030-4openalex-snapshot

Exine, onciform zone and intine structure in Ravenala and Phenakospermum and early wall development in Strelitzia and Phenakospermum (Strelitziaceae) based on aborted microspores

inferredcites →https://doi.org/10.1016/s0367-2530(17)31423-8openalex-snapshot

The Johnsonieae (Liliaceae); Biology and Classification1)1)Paper presented at the Symposium on the classification of the Liliiflorae at the XIII International Botanical Congress

inferredcites →https://doi.org/10.1016/s0367-2530(17)32225-9openalex-snapshot

Pollination Ecology and Seed Set in Asphodelus albus (Liliaceae) in Northern Spain

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/10.1017/cbo9781139002950.015openalex-snapshot

Contrasting patterns of support among plastid genes and genomes for major clades of the monocotyledons

inferredcites →https://doi.org/10.1017/s009483730000974xopenalex-snapshot

Angiosperm diversification and Cretaceous floristic trends: a comparison of palynofloras and leaf macrofloras

inferredcites →https://doi.org/10.1021/ac60199a736openalex-snapshot

Eberbach CORPORATION

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.0016-8025.2001.00817.xopenalex-snapshot

Similarity and diversity in adventitious root anatomy as related to root aeration among a range of wetland and dryland grass species

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/10.1046/j.1095-8339.2002.138002123.xopenalex-snapshot

Phylogenetics of Dioscoreales based on combined analyses of morphological and molecular data

inferredcites →https://doi.org/10.1046/j.1095-8339.2003.t01-1-00158.xopenalex-snapshot

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

inferredcites →https://doi.org/10.1071/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/10.1071/sb08040openalex-snapshot

Polyaperturate pollen types and ratios of heteromorphism in the monocot genus Conostylis (Haemodoraceae)

inferredcites →https://doi.org/10.1073/pnas.0407174101openalex-snapshot

Araceae from the Early Cretaceous of Portugal: Evidence on the emergence of monocotyledons

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.080421597openalex-snapshot

Early Cretaceous lineages of monocot flowering plants

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.1001225107openalex-snapshot

An uncorrelated relaxed-clock analysis suggests an earlier origin for flowering plants

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/10.1080/001731300750044582openalex-snapshot

Pollen walls of Araceae, with special reference to their fossilization potential

inferredcites →https://doi.org/10.1080/001731300750044609openalex-snapshot

Pollen morphology in the family Asphodelaceae (Asphodeleae, Kniphofieae)

inferredcites →https://doi.org/10.1080/001731300750044672openalex-snapshot

Contributions to the pollen morphology and taxonomy of the Liliaceae

inferredcites →https://doi.org/10.1080/001731300750044708openalex-snapshot

Comparison of different treatments for LM and SEM studies and systematic value of pollen grains in Cyperaceae

inferredcites →https://doi.org/10.1080/00173130152591859openalex-snapshot

Palynology of the perigoniate Aroideae: Zamioculcas, Gonatopus and Stylochaeton (Araceae)

inferredcites →https://doi.org/10.1080/00173130152591877openalex-snapshot

Pollen aperture morphology in Arecaceae: Application within phylogenetic analyses, and a summary of record of palm-like pollen the fossil

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

Triporate pollen in the Arecaceae

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/10.1080/00173130701780427openalex-snapshot

Pollen morphology and ultrastructure of Saururaceae

inferredcites →https://doi.org/10.1080/00173130701860104openalex-snapshot

Pollen morphology of Turkish Amaryllidaceae, Ixioliriaceae and Iridaceae

inferredcites →https://doi.org/10.1080/00173130903566723openalex-snapshot

Unique aperture stratification inCarex(Cyperaceae) pollen

inferredcites →https://doi.org/10.1080/00173134.1977.11864634openalex-snapshot

Pollen Morphology of Some Members of the Restionaceae and Related Families, with Notes on the Fossil Record

inferredcites →https://doi.org/10.1080/00173134.2010.512364openalex-snapshot

Upper Cretaceous sulcate pollen from the Timerdyakh Formation, Vilui Basin (Siberia)

inferredcites →https://doi.org/10.1080/00173134.2010.529503openalex-snapshot

Pollen morphology and infrageneric classification ofAlstroemeriaL. (Alstroemeriaceae)

inferredcites →https://doi.org/10.1080/00173136409430019openalex-snapshot

The Fine Structure of the Pollen Grain of Clivia Miniata

inferredcites →https://doi.org/10.1080/00173136609430033openalex-snapshot

On the Pollen Morphology of the Centrolepidaceae, Restionaceae and Flagellariaceae, with Special Reference to Taxonomy

inferredcites →https://doi.org/10.1080/00173136709432845openalex-snapshot

Apertural Types in Pollen of the Restionaceae and Flagellariaceae

inferredcites →https://doi.org/10.1080/00173137109430488openalex-snapshot

Pollen of the Butomaceae and Alismataceae

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

Pollen Morphology of the Family Magnoliaceae

inferredcites →https://doi.org/10.1080/00173138009424981openalex-snapshot

On the Development of the Reticulate Structure ofHemerocallisPollen (Liliaceae)

inferredcites →https://doi.org/10.1080/00173138009424982openalex-snapshot

Pollen Morphology of the Tribe Neottieae and its Impact on the Classification of the Orchidaceae

inferredcites →https://doi.org/10.1080/00173138009425001openalex-snapshot

The Pollen of the Austrobaileyaceae and its Phylogenetic Significance

inferredcites →https://doi.org/10.1080/00173138209427690openalex-snapshot

Nature of the sporoderm in monocotyledons, with special reference to the pollen grains ofcannaandheliconia

inferredcites →https://doi.org/10.1080/00173138309431969openalex-snapshot

Pollen ultrastructure of the Haemodoraceae and its taxonomic significance

inferredcites →https://doi.org/10.1080/00173138509427420openalex-snapshot

Pollen Ultrastructure of the Philydraceae

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/10.1080/00173138709428914openalex-snapshot

Developmental Evidence for the Convergence ofSassafras(Laurales) andHeliconia(Zingiberales) Pollen

inferredcites →https://doi.org/10.1080/00173138709429941openalex-snapshot

Pollen ultrastructure of the Pontederiaceae

inferredcites →https://doi.org/10.1080/00173138809429948openalex-snapshot

Phylogenetic trends in the Alismatales with reference to pollen grains

inferredcites →https://doi.org/10.1080/00173138809429953openalex-snapshot

Biopalynological Study ofLapageria roseaandIris Unguicularis: Storage of Pollen

inferredcites →https://doi.org/10.1080/00173139209432032openalex-snapshot

Morphologie und systematische Bedeutung des Pollens der Bromeliaceae

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/10.1080/00173139309429459openalex-snapshot

Sulcus morphology in some monocot families

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/10.1080/00173139609429077openalex-snapshot

Ontogeny of pollen grains inZingiber spectabile(Zingiberaceae)

inferredcites →https://doi.org/10.1080/00173139609430497openalex-snapshot

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

inferredcites →https://doi.org/10.1080/00173139809362647openalex-snapshot

Pollen morphology ofOryza(Poaceae)

inferredcites →https://doi.org/10.1080/00173139809362687openalex-snapshot

Microsporogenesis and pollen morphology in dioscoreales and allied taxa

inferredcites →https://doi.org/10.1080/0021213x.1979.10676858openalex-snapshot

NYMPHAEA REVISITED: A PRELIMINARY COMMUNICATION

inferredcites →https://doi.org/10.1080/0028825x.1966.10429041openalex-snapshot

Australasian asteliads (Liliaceae)

inferredcites →https://doi.org/10.1080/0028825x.1972.10430252openalex-snapshot

Biological flora of New Zealand 7. Ripogonum scandens J. R. et G. Forst. (Smilacaceae) Supplejack, Kareao

inferredcites →https://doi.org/10.1080/00378941.1888.10830399openalex-snapshot

Sur Les Affinités Du GenreSusum

inferredcites →https://doi.org/10.1080/106351501753462885openalex-snapshot

Unraveling the Evolutionary Radiation of the Families of the Zingiberales Using Morphological and Molecular Evidence

inferredcites →https://doi.org/10.1080/12538078.1994.10515157openalex-snapshot

Comparative pollen structure and pollination biology in theCallitrichaceae

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

Systematics of Acorus: Ovule and Anther

inferredcites →https://doi.org/10.1086/297592openalex-snapshot

The Spiny Pollen Wall in Sauromatum (Araceae)-with Special Reference to the Endexine

inferredcites →https://doi.org/10.1086/314099openalex-snapshot

Beetle Pollination and Floral Thermogenicity inMagnoliaTamaulipana(Magnoliaceae)

inferredcites →https://doi.org/10.1086/314122openalex-snapshot

The Basic Pollen Wall Types in Araceae

inferredcites →https://doi.org/10.1086/314129openalex-snapshot

Inaperturate Pollen in Monocotyledons

inferredcites →https://doi.org/10.1086/314162openalex-snapshot

Systematic Position ofXyris: Flower and Seed Anatomy

inferredcites →https://doi.org/10.1086/314241openalex-snapshot

Floral Structure and Development of Acoraceae and Its Systematic Relationships with Basal Angiosperms

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

Pollen Diversity in Some Modern Magnoliids

inferredcites →https://doi.org/10.1086/317575openalex-snapshot

New Perspectives on the Pollination Biology of 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/10.1086/317584openalex-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/10.1086/321919openalex-snapshot

The Flowers in Extant Basal Angiosperms and Inferences on Ancestral Flowers

inferredcites →https://doi.org/10.1086/336770openalex-snapshot

Pollen Studies in the Alismataceae (Alismaceae)

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

Pollen Wall Development of Austrobaileya maculata

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

Morphological Phylogenetic Analysis of Living and Fossil Chloranthaceae

inferredcites →https://doi.org/10.1086/407701openalex-snapshot

Fossil Evidence on Early Evolution of the Monocotyledons

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/10.1086/499503openalex-snapshot

Comparative Structure and Development of Pollen and Tapetum in Pandanales

inferredcites →https://doi.org/10.1086/503444openalex-snapshot

Bayesian Analysis of Correlated Evolution of Discrete Characters by Reversible‐Jump Markov Chain Monte Carlo

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/10.1086/654848openalex-snapshot

Pollen Evolution in the Early‐Divergent Monocot Order Alismatales

inferredcites →https://doi.org/10.1093/aob/mcf138openalex-snapshot

Types of Pollen Dispersal Units in Orchids, and their Consequences for Germination and Fertilization

inferredcites →https://doi.org/10.1093/aob/mci030openalex-snapshot

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

inferredcites →https://doi.org/10.1093/aob/mcl125openalex-snapshot

Early Angiosperm Ecology: Evidence from the Albian-Cenomanian of Europe

inferredcites →https://doi.org/10.1093/aob/mcl287openalex-snapshot

Pollination of Schisandra henryi (Schisandraceae) by Female, Pollen-eating Megommata Species (Cecidomyiidae, Diptera) in South-central China

inferredcites →https://doi.org/10.1093/aob/mcq075openalex-snapshot

A new look at sporoderm ontogeny in Persea americana and the hidden side of development

inferredcites →https://doi.org/10.1093/aob/mcr008openalex-snapshot

Reproductive biology of Abolboda pulchella and A. poarchon (Xyridaceae: Poales)

inferredcites →https://doi.org/10.1093/aob/mct264openalex-snapshot

Resolving ancient radiations: can complete plastid gene sets elucidate deep relationships among the tropical gingers (Zingiberales)?

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/jxb/erg242openalex-snapshot

Rate of dehydration of corn (Zea mays L.) pollen in the air

inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a085120openalex-snapshot

Studies on Pollination in Musaceae

inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a086169openalex-snapshot

Reproduction in Seagrasses: Pollen Development in Thalassia hemprichii, Halophila stipulacea and Thalassodendron ciliatum

inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a086415openalex-snapshot

Pollen Wall Structure and Cytochemistry in the Seagrass Amphibolis griffithii (Cymodoceaceae)

inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a087840openalex-snapshot

Pollen Wall Development of Xiphidium coeruleum (Haemodoraceae) and its Systematic Implications

inferredcites →https://doi.org/10.1093/sysbio/42.4.576openalex-snapshot

Missing Data Versus Missing Characters in Phylogenetic Analysis

inferredcites →https://doi.org/10.1097/00010694-195402000-00021openalex-snapshot

New Zealand Pollen Studies. Bulletin No. 3 Auckland Institute and Museum

inferredcites →https://doi.org/10.1098/rspb.1994.0006openalex-snapshot

Detecting correlated evolution on phylogenies: a general method for the comparative analysis of discrete characters

inferredcites →https://doi.org/10.1098/rstb.2004.1531openalex-snapshot

South American palaeobotany and the origins of neotropical rainforests

inferredcites →https://doi.org/10.1105/tpc.015800openalex-snapshot

Pollen and Stigma Structure and Function: The Role of Diversity in Pollination

inferredcites →https://doi.org/10.1111/boj.12160openalex-snapshot

A revised evolutionary history of Poales: origins and diversification

inferredcites →https://doi.org/10.1111/boj.12385openalex-snapshot

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

inferredcites →https://doi.org/10.1111/j.1095-8339.1990.tb00195.xopenalex-snapshot

Palynology of South Indian Zingiberaceae

inferredcites →https://doi.org/10.1111/j.1095-8339.2003.00227.xopenalex-snapshot

Pollen morphology of Dioscorea (Dioscoreaceae) and its relation to systematics

inferredcites →https://doi.org/10.1111/j.1095-8339.2004.00345.xopenalex-snapshot

The age of major monocot groups inferred from 800+rbcL sequences

inferredcites →https://doi.org/10.1111/j.1095-8339.2005.00386.xopenalex-snapshot

A phenetic analysis and revision of Guineo-Congolean rain forest taxa of Chlorophytum (Anthericaceae)

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.1095-8339.2010.01093.xopenalex-snapshot

Pollen morphology of selected Central European species from subgenera Vignea and Carex (Carex, Cyperaceae) and its relation to taxonomy

showing the first 200 of 312

What points at this work

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

inferred← citeshttps://doi.org/10.11646/phytotaxa.275.2.2zenodo-depositor-declared

A new family placement for Australian blue squill, Chamaescilla: Xanthorrhoeaceae (Hemerocallidoideae), not Asparagaceae

inferred← citeshttps://doi.org/10.1002/ajb2.1326openalex-snapshot

How does genome size affect the evolution of pollen tube growth rate, a haploid performance trait?

inferred← citeshttps://doi.org/10.1007/s00497-023-00484-5openalex-snapshot

Pollen viability, longevity, and function in angiosperms: key drivers and prospects for improvement

inferred← citeshttps://doi.org/10.1007/s00709-025-02103-8openalex-snapshot

A new model for the global patterning of spores and pollen grains

inferred← citeshttps://doi.org/10.1007/s12229-026-09328-zopenalex-snapshot

Pollen Diversity in Bromeliaceae (Poales): A Morphological and Micromorphological Review

inferred← citeshttps://doi.org/10.1007/s40415-021-00719-7openalex-snapshot

Pollen morphology and evolutionary history of Sapindales

inferred← citeshttps://doi.org/10.1016/j.flora.2023.152342openalex-snapshot

Pollen morphology and variability among the wild Cannabis sativa L. from the western Himalaya, India

inferred← citeshttps://doi.org/10.1016/j.flora.2026.152949openalex-snapshot

An illustrated key for the identification of pollen grains from Rudraprayag District, Garhwal Himalaya, India

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/10.1016/j.revpalbo.2023.104953openalex-snapshot

Algal association and angiosperm diversification from the early Cretaceous (Springhill Formation) of Patagonia: Insights into palaeoclimate and aquatic environments at Río Correntoso locality, Argentina

inferred← citeshttps://doi.org/10.1016/j.scienta.2023.112513openalex-snapshot

Endocellulase SlGH9-21 significantly improves drought resistance and storage capacity of tomato

inferred← citeshttps://doi.org/10.1016/j.ympev.2017.01.015openalex-snapshot

Plastid phylogenomics and adaptive evolution of Gaultheria series Trichophyllae (Ericaceae), a clade from sky islands of the Himalaya-Hengduan Mountains

inferred← citeshttps://doi.org/10.1016/j.ympev.2018.12.023openalex-snapshot

Plastid phylogenomic insights into the evolution of Caryophyllales

inferred← citeshttps://doi.org/10.1080/00173134.2022.2127328openalex-snapshot

Systematics of Zingiberaceae

inferred← citeshttps://doi.org/10.1080/23818107.2019.1652849openalex-snapshot

Microsporogenesis in angiosperms producing pantoporate pollen

inferred← citeshttps://doi.org/10.1088/1755-1315/276/1/012031openalex-snapshot

Identification of Pollen Grains Morphology and Morphometry in Liliaceae

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/gbe/evv260openalex-snapshot

Plastid Phylogenomic Analyses Resolve Tofieldiaceae as the Root of the Early Diverging Monocot Order Alismatales

inferred← citeshttps://doi.org/10.1093/gigascience/giae006openalex-snapshot

A reference genome of Commelinales provides insights into the commelinids evolution and global spread of water hyacinth (Pontederia crassipes)

inferred← citeshttps://doi.org/10.1105/tpc.20.00551openalex-snapshot

Grass-Specific EPAD1 Is Essential for Pollen Exine Patterning in Rice

inferred← citeshttps://doi.org/10.1111/1755-6724.70035openalex-snapshot

Ultrastructural Observation of Quantonenpollenites , a Characteristic Pollen of the Quantou Formation in the Songliao Basin, and its Taxonomic Clarification

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

Climate adaptation and functional constraints drive pollen evolution in Apiales

inferred← citeshttps://doi.org/10.15835/nbha50312787openalex-snapshot

Palynological diversity of highly medicinal rare, endangered, and threatened plants from Western Himalaya, India

inferred← citeshttps://doi.org/10.21203/rs.3.rs-4304937/v1openalex-snapshot

Exploring palynological diversity of Some concrete Honey Bee Forage Plants in North-Eastern Himalayas, India

inferred← citeshttps://doi.org/10.3390/molecules22111875openalex-snapshot

The Complete Amomum kravanh Chloroplast Genome Sequence and Phylogenetic Analysis of the Commelinids

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/10.36808/if/2025/v151i2/170469openalex-snapshot

Pollen Morphology of Some Selected Taxa in the Jorhat District, Assam, India

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