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Evolution of Angiosperm Pollen. 5. Early Diverging Superasteridae (Berberidopsidales, Caryophyllales, Cornales, Ericales, and Santalales) Plus Dilleniales
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1537-2197.1964.tb06616.xopenalex-snapshot
BIOSYSTEMATIC STUDIES IN THE BOUTELOUA CURTIPENDULA COMPLEX. III. POLLEN SIZE AS RELATED TO CHROMOSOME NUMBERS
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.tb07622.xopenalex-snapshot
FINE STRUCTURE OF MISTLETOE POLLEN. III. LARGE‐FLOWERED NEOTROPICAL LORANTHACEAE AND THEIR AUSTRALIAN RELATIVES
inferredcites →https://doi.org/10.1002/j.1537-2197.1982.tb13230.xopenalex-snapshot
FINE STRUCTURE OF MISTLETOE POLLEN. IV. EURASIAN AND AUSTRALIAN VISCUM L. (VISCACEAE)
inferredcites →https://doi.org/10.1002/j.1537-2197.1982.tb13248.xopenalex-snapshot
FINE STRUCTURE OF MISTLETOE POLLEN. V. MADAGASCAN AND CONTINENTAL AFRICAN VISCUM L. (VISCACEAE)
inferredcites →https://doi.org/10.1002/j.1537-2197.1982.tb13351.xopenalex-snapshot
POLLEN MORPHOLOGY OF THE DILLENIACEAE AND ACTINIDIACEAE
inferredcites →https://doi.org/10.1002/j.1537-2197.1984.tb12505.xopenalex-snapshot
POLLEN MORPHOLOGY AND THE RELATIONSHIPS OF SIMMONDSIA CHINENSIS TO THE ORDER EUPHORBIALES
inferredcites →https://doi.org/10.1002/j.1537-2197.1990.tb13524.xopenalex-snapshot
POLLEN MORPHOLOGY AND SYSTEMATICS OF SIPHONOGLOSSA SENSU LATO (ACANTHACEAE)
inferredcites →https://doi.org/10.1002/j.1537-2197.1993.tb15239.xopenalex-snapshot
POLLEN MORPHOLOGY, TRICHOME TYPES, AND RELATIONSHIPS OF THE GRONOVIOIDEAE (LOASACEAE)
inferredcites →https://doi.org/10.1002/j.1537-2197.1995.tb11491.xopenalex-snapshot
S ize‐number trade‐offs and pollen production by P apilionaceous legumes
inferredcites →https://doi.org/10.1002/j.1537-2197.1996.tb12792.xopenalex-snapshot
The pollen morphology of Vicia (Leguminosae)
inferredcites →https://doi.org/10.1002/tax.591021openalex-snapshot
Disintegrating Portulacaceae: A new familial classification of the suborder Portulacineae (Caryophyllales) based on molecular and morphological data
inferredcites →https://doi.org/10.1002/tax.592019openalex-snapshot
A revised classification of Santalales
inferredcites →https://doi.org/10.1002/tax.603010openalex-snapshot
Phylogenetic signal of orbicules at family level: Rubiaceae as case study
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.2000.0380openalex-snapshot
Angiosperm phylogeny inferred from 18S rDNA, rbcL, and atpB sequences
inferredcites →https://doi.org/10.1007/978-3-642-78220-6_8openalex-snapshot
Pollen Morphology and Exine Ultrastructure
inferredcites →https://doi.org/10.1007/978-3-7091-6612-3_7openalex-snapshot
Palynology and systematics of Ranunculiflorae
inferredcites →https://doi.org/10.1007/bf00937780openalex-snapshot
Pollen grain morphology ofCoris (Primulaceae)
inferredcites →https://doi.org/10.1007/bf00937832openalex-snapshot
Pollination biology and sexual differentiation ofOsyris alba (Santalaceae) in the Mediterranean region
inferredcites →https://doi.org/10.1007/bf00983214openalex-snapshot
Implications ofrbcL sequence data for higher order relationships of theLoasaceae and the anomalous aquatic plantHydrostachys (Hydrostachyaceae)
inferredcites →https://doi.org/10.1007/bf00984117openalex-snapshot
Ultrastructural, micromorphological and phytochemical evidence for a ?Central Position? ofMacarthuria (Molluginaceae) within theCaryophyllales
inferredcites →https://doi.org/10.1007/bf00984559openalex-snapshot
Zur Skulptur der Pollen-Exine bei drei Centrospermen (Gisekia, Limeum, Hectorella), bei Gyrostemonaceen und Rhabdodendraceen
inferredcites →https://doi.org/10.1007/bf00986074openalex-snapshot
Ultrastructure of pollen exine in centrospermous families
inferredcites →https://doi.org/10.1007/bf01373229openalex-snapshot
Pollen morphology and its relationships to taxonomy and distribution ofTamarix, seriesVaginantes
inferredcites →https://doi.org/10.1007/bf01379643openalex-snapshot
Morphological and embryological studies in the family loranthaceae. XII.Moquiniella rubra (Spreng. f.)Balle
inferredcites →https://doi.org/10.1007/bf01678036openalex-snapshot
Pollen grain size in four ploidy levels of genusAvena
inferredcites →https://doi.org/10.1007/bf02101124openalex-snapshot
Phylogenetic relationships of the Santalales and relatives
inferredcites →https://doi.org/10.1007/bf02488560openalex-snapshot
Pollen morphology of JapaneseSymplocos (Symplocaceae)
inferredcites →https://doi.org/10.1007/bf02853372openalex-snapshot
Pollen morphology in thePortulacaceae (Centrospermae)
inferredcites →https://doi.org/10.1007/bf02857950openalex-snapshot
Taxonomic affinities ofPhysena (Physenaceae) andAsteropeia (Theaceae)
inferredcites →https://doi.org/10.1007/bf02860849openalex-snapshot
Early cretaceous fossil evidence for angiosperm evolution
inferredcites →https://doi.org/10.1007/s00606-005-0334-4openalex-snapshot
Pollen morphology of the genera Polygonum s. str. and Polygonella (Polygoneae: Polygonaceae)
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/s00606-008-0142-8openalex-snapshot
Pollen grain size, stigma depth, and style length: the relationships revisited
inferredcites →https://doi.org/10.1007/s00606-009-0262-9openalex-snapshot
Pollen morphology and its phylogenetic significance in tribe Sanguisorbeae (Rosaceae)
inferredcites →https://doi.org/10.1007/s10265-002-0044-8openalex-snapshot
Pollen-pistil relationships and pollen size-number trade-off in species of the tribe Lycieae (Solanaceae)
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/10.1016/0034-6667(67)90202-3openalex-snapshot
Pollen morphology and taxonomy of the family polemoniaceae
inferredcites →https://doi.org/10.1016/0034-6667(70)90028-xopenalex-snapshot
Pollen morphology of the alangiaceae
inferredcites →https://doi.org/10.1016/0034-6667(72)90030-9openalex-snapshot
On the pollen morphology of convolvulaceae with special reference to taxonomy
inferredcites →https://doi.org/10.1016/0195-6671(92)90039-sopenalex-snapshot
Revised palynological correlations of the lower Potomac group (USA) and the cocobeach sequence of Gabon (Barremian-Aptian)
inferredcites →https://doi.org/10.1016/j.revpalbo.2005.12.001openalex-snapshot
Merging concepts: The role of self-assembly in the development of pollen wall structure
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.2007.01.002openalex-snapshot
Pollen morphology of Austrocylindropuntia Backeb, Maihueniopsis Speg., Opuntia Mill. and Tephrocactus Lem. (Cactaceae, Opuntioideae) of Argentina
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.2008.10.001openalex-snapshot
Systematic palynology in Ebenaceae with focus on Ebenoideae: Morphological diversity and character evolution
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.2013.01.003openalex-snapshot
Atlas of the tropical West African pollen flora
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.2015.07.010openalex-snapshot
Genetic and Biochemical Mechanisms of Pollen Wall Development
inferredcites →https://doi.org/10.1016/j.ympev.2003.09.014openalex-snapshot
Conflicting phylogenies of balsaminoid families and the polytomy in Ericales: combining data in a Bayesian framework
inferredcites →https://doi.org/10.1016/j.ympev.2009.01.017openalex-snapshot
Phylogeny and biogeography of Alangiaceae (Cornales) inferred from DNA sequences, morphology, and fossils
inferredcites →https://doi.org/10.1016/j.ympev.2010.02.028openalex-snapshot
Molecular phylogenetic relationships and a revised classification of the subfamily Ericoideae (Ericaceae)
inferredcites →https://doi.org/10.1016/j.ympev.2011.01.016openalex-snapshot
Resolving and dating the phylogeny of Cornales – Effects of taxon sampling, data partitions, and fossil calibrations
inferredcites →https://doi.org/10.1016/s0034-6667(98)00045-1openalex-snapshot
Hypothetical way of pollen aperture patterning. 1: Formation of 3-colpate patterns and endoaperture geometry
inferredcites →https://doi.org/10.1016/s0034-6667(99)00057-3openalex-snapshot
Hypothetical way of pollen aperture patterning. 2. Formation of polycolpate patterns and pseudoaperture geometry
inferredcites →https://doi.org/10.1016/s0367-1615(17)32481-3openalex-snapshot
Die Pollenmorphologie der europäischen Cornus-Arten und einiger ähnlicher Pollentypen
inferredcites →https://doi.org/10.1016/s1055-7903(02)00240-3openalex-snapshot
Phylogenetics of asterids based on 3 coding and 3 non-coding chloroplast DNA markers and the utility of non-coding DNA at higher taxonomic levels
inferredcites →https://doi.org/10.1016/s1055-7903(02)00267-1openalex-snapshot
Relationships within Cornales and circumscription of Cornaceae—matK and rbcL sequence data and effects of outgroups and long branches
inferredcites →https://doi.org/10.1017/s0094837300015864openalex-snapshot
Discordance and concordance between morphological and taxonomic diversity
inferredcites →https://doi.org/10.1023/a:1023210407163openalex-snapshot
LH-β and FSH-β mRNA expression in nesting and post-breeding three-spined stickleback, Gasterosteus aculeatus, and effects of castration on expression of LH-β, FSH-β and spiggin mRNA
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/nmeth.2109openalex-snapshot
jModelTest 2: more models, new heuristics and parallel computing
inferredcites →https://doi.org/10.1043/0363-6445-26.2.406openalex-snapshot
Phylogeny of the Portulacaceous Cohort Based on ndhF Sequence 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/10.1055/s-2000-9460openalex-snapshot
Molecular Phylogeny of Caryophyllidae s.l. Based on MatK Sequences with Special Emphasis on Carnivorous Taxa
inferredcites →https://doi.org/10.1055/s-2001-12897openalex-snapshot
Molecular Phylogeny of Nepenthaceae Based on Cladistic Analysis of Plastid trnK Intron Sequence Data
inferredcites →https://doi.org/10.1055/s-2006-924460openalex-snapshot
Molecular Phylogeny and Character Evolution of Carnivorous Plant Families in Caryophyllales — Revisited
inferredcites →https://doi.org/10.1073/pnas.0305562101openalex-snapshot
Mitochondrial DNA sequences reveal the photosynthetic relatives of Rafflesia , the world's largest flower
inferredcites →https://doi.org/10.1073/pnas.0907801107openalex-snapshot
Phylogenetic analysis of 83 plastid genes further resolves the early diversification of eudicots
inferredcites →https://doi.org/10.1080/001731302321011997openalex-snapshot
Pollen morphology in the ericoid clade of the order Ericales, with special emphasis on Cyrillaceae
inferredcites →https://doi.org/10.1080/00173130410016760openalex-snapshot
The conserved nature and taxonomic utility of pollen morphology inCantua(Polemoniaceae)
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/10.1080/00173130500477688openalex-snapshot
A survey of species assigned to the fossil pollen genusAnacolosidites
inferredcites →https://doi.org/10.1080/00173130500477787openalex-snapshot
Multiple origins of a unique pollen feature: stellate pore ornamentation in Amaranthaceae
inferredcites →https://doi.org/10.1080/00173130500477902openalex-snapshot
Pollen morphology and systematics of Burseraceae
inferredcites →https://doi.org/10.1080/00173130600873935openalex-snapshot
Pollen morphology and systematics of Atripliceae (Chenopodiaceae)
inferredcites →https://doi.org/10.1080/00173134.1975.11864622openalex-snapshot
Pollen Morphology in the Order Centrospermae
inferredcites →https://doi.org/10.1080/00173134.1975.11864624openalex-snapshot
Pollen Morphology of Polemoniaceae in Relation to Systematics and Pollination Systems: Scanning Electron Microscopy
inferredcites →https://doi.org/10.1080/00173134.1977.11864635openalex-snapshot
Pollen Morphology of East African Caryophyllaceae
inferredcites →https://doi.org/10.1080/00173134.2013.819526openalex-snapshot
Pollen morphology of Justicia L. (Acanthaceae) from Thailand and its taxonomic value
inferredcites →https://doi.org/10.1080/00173134.2016.1159729openalex-snapshot
Pollen wall and tapetum development inPlantago majorL. (Plantaginaceae): assisting self-assembly
inferredcites →https://doi.org/10.1080/00173136309429110openalex-snapshot
Pollen Morphology of the Cactaceae
inferredcites →https://doi.org/10.1080/00173136709430042openalex-snapshot
Studies in Montia L. and Claytonia L. and Allied Genera
inferredcites →https://doi.org/10.1080/00173136709432849openalex-snapshot
Pollen Morphology in the Polemoniaceae
inferredcites →https://doi.org/10.1080/00173137009427388openalex-snapshot
Pollen Morphology in the Nyctaginaceae
inferredcites →https://doi.org/10.1080/00173137009427397openalex-snapshot
The Pollen Morphology of the Haloragaceae with Reference to Taxonomy
inferredcites →https://doi.org/10.1080/00173137309428841openalex-snapshot
Pollen Morphology ofBarringtonia CalyptrocalyxK. Sch. (Lecythidaceae)
inferredcites →https://doi.org/10.1080/00173137309429884openalex-snapshot
Pollen Morphology within the GenusDrosera
inferredcites →https://doi.org/10.1080/00173137409434771openalex-snapshot
Pollen Grains of Some American Olacaceae
inferredcites →https://doi.org/10.1080/00173137909430723openalex-snapshot
Pollen morphology of BrazilianSymplocosspecies (Symplocaceae)
inferredcites →https://doi.org/10.1080/00173138709428915openalex-snapshot
Pollen Morphology of Tribulaceae
inferredcites →https://doi.org/10.1080/00173139209427822openalex-snapshot
Comparative pollen morphology of the styracaceae
inferredcites →https://doi.org/10.1080/00173139509429039openalex-snapshot
Pollen Morphology ofParapteropyrumand Some Putatively Related Genera (Polygonaceae – Atraphaxideae)
inferredcites →https://doi.org/10.1080/00173139809362658openalex-snapshot
Pollen types in the Amaranthaceae. Morphology and evolutionary significance
inferredcites →https://doi.org/10.1080/01916122.2014.932859openalex-snapshot
The palynology of Aizoaceae and Molluginaceae in Egypt and Sudan
inferredcites →https://doi.org/10.1080/10635150119871openalex-snapshot
Empirical and Hierarchical Bayesian Estimation of Ancestral States
inferredcites →https://doi.org/10.1080/106351598260996openalex-snapshot
Is It Better to Add Taxa or Characters to a Difficult Phylogenetic Problem?
inferredcites →https://doi.org/10.1086/317578openalex-snapshot
Morphological Phylogenetic Analysis of Basal Angiosperms: Comparison and Combination with Molecular Data
inferredcites →https://doi.org/10.1086/337715openalex-snapshot
Ontogenetic Development of Pollen Tetrads of Drosera capensis L.
inferredcites →https://doi.org/10.1086/337776openalex-snapshot
Pollen Morphology and Relationship of Symplocos tinctoria (L.F.) L'Her. (Symplocaceae)
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/10.1086/523364openalex-snapshot
Function and Evolution of Aggregated Pollen in Angiosperms
inferredcites →https://doi.org/10.1086/597785openalex-snapshot
Phylogeny of the Caryophyllales Sensu Lato: Revisiting Hypotheses on Pollination Biology and Perianth Differentiation in the Core Caryophyllales
inferredcites →https://doi.org/10.1086/599239openalex-snapshot
Phylogenetics of Dilleniaceae Using Sequence Data from Four Plastid Loci (rbcL,infA,rps4,rpl16Intron)
inferredcites →https://doi.org/10.1086/648993openalex-snapshot
A New Lineage‐Based Tribal Classification of the Family Caryophyllaceae
inferredcites →https://doi.org/10.1086/658923openalex-snapshot
Phylogenetic Analysis of the Plastid Inverted Repeat for 244 Species: Insights into Deeper-Level Angiosperm Relationships from a Long, Slowly Evolving Sequence Region
inferredcites →https://doi.org/10.1086/667588openalex-snapshot
Testing for Ecological Limitation of Diversification: A Case Study Using Parasitic Plants
inferredcites →https://doi.org/10.1093/aob/mci256openalex-snapshot
Palynological Variation in Balsaminoid Ericales. I. Marcgraviaceae
inferredcites →https://doi.org/10.1093/aob/mci257openalex-snapshot
Palynological Variation in Balsaminoid Ericales. II. Balsaminaceae, Tetrameristaceae, Pellicieraceae and General Conclusions
inferredcites →https://doi.org/10.1093/sysbio/27.4.401openalex-snapshot
Cases in which Parsimony or Compatibility Methods will be Positively Misleading
inferredcites →https://doi.org/10.1097/00010694-195303000-00016openalex-snapshot
Pollen Morphology and Plant Taxonomy
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.1095-8339.2007.00694.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.1095-8339.2012.01241.xopenalex-snapshot
Evolution and phylogenetic significance of pollen in Annonaceae
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.1475-4983.2006.00614.xopenalex-snapshot
DISPARITY: MORPHOLOGICAL PATTERN AND DEVELOPMENTAL CONTEXT
inferredcites →https://doi.org/10.1111/j.1756-1051.1981.tb01159.xopenalex-snapshot
Pollen morphology and relationships of the Misodendraceae (Santalales)
inferredcites →https://doi.org/10.1111/j.1759-6831.2009.00058.xopenalex-snapshot
Integrating Early Cretaceous fossils into the phylogeny of living angiosperms: Magnoliidae and eudicots
inferredcites →https://doi.org/10.1111/jipb.12477openalex-snapshot
Pollen size strongly correlates with stigma depth among Pedicularis species
inferredcites →https://doi.org/10.1111/nph.14503openalex-snapshot
Resolution of deep eudicot phylogeny and their temporal diversification using nuclear genes from transcriptomic and genomic datasets
inferredcites →https://doi.org/10.1126/science.1523408openalex-snapshot
Carnivorous Plants: Phylogeny and Structural Evolution
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.209.4454.400openalex-snapshot
Intrafloral Pollen Differentiation in the New World Lecythidaceae, Subfamily Lecythidoideae
inferredcites →https://doi.org/10.1139/b74-041openalex-snapshot
Ultrastructure of pollen of Opuntia polyacantha
inferredcites →https://doi.org/10.1139/b78-341openalex-snapshot
Fine structure of mistletoe pollen. I. Eremolepidaceae, Lepidoceras, and Tupeia
inferredcites →https://doi.org/10.1139/b86-408openalex-snapshot
Distinguishing pollen characters for the Sapotaceae
inferredcites →https://doi.org/10.1146/annurev.ecolsys.28.1.129openalex-snapshot
The Evolution of Morphological Diversity
inferredcites →https://doi.org/10.11646/phytotaxa.181.4.4openalex-snapshot
On the disintegration of Molluginaceae: a new genus and family (Kewa, Kewaceae) segregated from Hypertelis, and placement of Macarthuria in Macarthuriaceae
inferredcites →https://doi.org/10.1186/1471-2148-14-23openalex-snapshot
From algae to angiosperms–inferring the phylogeny of green plants (Viridiplantae) from 360 plastid genomes
inferredcites →https://doi.org/10.1242/jcs.11.3.699openalex-snapshot
The Organization and Polarity of Pollen Mother Cells of Triticum Aestivum
inferredcites →https://doi.org/10.1600/036364407782250643openalex-snapshot
A Molecular Phylogeny of the Feathery Mistletoe Misodendrum
inferredcites →https://doi.org/10.1600/036364408783887384openalex-snapshot
Molecular Phylogenetic Relationships of Olacaceae and Related Santalales
inferredcites →https://doi.org/10.1600/036364408783887438openalex-snapshot
A Molecular Phylogeny of Santalaceae (Santalales)
inferredcites →https://doi.org/10.17129/botsci.2296openalex-snapshot
Morfología polínica de especies de la selva mediana subperennifolia en la cuenca del río Candelaria, Campeche
inferredcites →https://doi.org/10.2307/1219987openalex-snapshot
POLLEN FINE STRUCTURE AND RELATIONSHIPS OF ACHATOCARPUS TRIANA AND PHAULOTHAMNUS A. GRAY
inferredcites →https://doi.org/10.2307/2395088openalex-snapshot
Pollen Morphology and Relationships of the Flacourtiaceae
inferredcites →https://doi.org/10.2307/2395128openalex-snapshot
Palynotaxonomic Study of the Phytolaccaceae
inferredcites →https://doi.org/10.2307/2395271openalex-snapshot
The Bases of Angiosperm Phylogeny: Palynology
inferredcites →https://doi.org/10.2307/2398885openalex-snapshot
A Contribution to the Floral Biology and Reproductive System of Couroupita Guianensis Aubl. (Lecythidaceae)
inferredcites →https://doi.org/10.2307/2398913openalex-snapshot
Form and Function in Angiosperm Pollen
inferredcites →https://doi.org/10.2307/2398914openalex-snapshot
Pollen Morphology: The Potential Influence in Higher Order Systematics
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/10.2307/2399141openalex-snapshot
Notes on the Floral Biology of Couroupita guianensis Aubl. (Lecythidaceae)
inferredcites →https://doi.org/10.2307/2399176openalex-snapshot
Fine Structure of Mistletoe Pollen VI. Small-Flowered Neotropical Loranthaceae
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/10.2307/2399952openalex-snapshot
Angiosperm Phylogeny Inferred from 18S Ribosomal DNA Sequences
inferredcites →https://doi.org/10.2307/2419420openalex-snapshot
Phylogenetic Relationships in Cornus (Cornaceae)
inferredcites →https://doi.org/10.2307/2419422openalex-snapshot
Systematic Implications of Pollen Morphology in Caryopteris (Labiatae)
inferredcites →https://doi.org/10.2307/2419743openalex-snapshot
Phylogenetic Relationships in Sarraceniaceae Based on rbcL and ITS Sequences
inferredcites →https://doi.org/10.2307/2419747openalex-snapshot
Pollen Morphology, Exine Structure and the Relationships of Basellaceae and Didiereaceae to Portulacaceae
inferredcites →https://doi.org/10.2307/2656679openalex-snapshot
The cytoskeleton and polarization during pollen development in Carex blanda (Cyperaceae)
inferredcites →https://doi.org/10.2307/2656868openalex-snapshot
The questionable relationship of Montinia (Montiniaceae): evidence from a floral ontogenetic and anatomical study
inferredcites →https://doi.org/10.2307/2805095openalex-snapshot
Biosystematic Studies in the Bouteloua curtipendula Complex II. Taxonomy
inferredcites →https://doi.org/10.2307/2844614openalex-snapshot
Fossil Pollen of Ximenia (Olacaceae) in the Lower Pleistocene of Olduvai, Tanzania: Palaeocological Implications
inferredcites →https://doi.org/10.2307/2992015openalex-snapshot
An Ordinal Classification for the Families of Flowering Plants
inferredcites →https://doi.org/10.2307/4110538openalex-snapshot
The Pollen Morphology of the Sapotaceae
inferredcites →https://doi.org/10.2307/4114634openalex-snapshot
The Embryology, Reproductive Morphology and Systematics of Lecythidaceae
inferredcites →https://doi.org/10.2307/4115644openalex-snapshot
Phylogeny of the Eudicots: A Nearly Complete Familial Analysis Based on rbcL Gene Sequences
inferredcites →https://doi.org/10.2307/4117819openalex-snapshot
Familial Relationships of Rhabdodendron (Rhabdodendraceae): Plastid rbcL Sequences Indicate a Caryophyllid Placement
inferredcites →https://doi.org/10.2307/4129957openalex-snapshot
Delimitation and Infra-Generic Classification of Justicia (Acanthaceae)
inferredcites →https://doi.org/10.25223/brad.n15.1997.a11openalex-snapshot
Pollen morphology of some Cactaceae of North-Eastern Brazil
inferredcites →https://doi.org/10.3119/0035-4902-113.955.235openalex-snapshot
Pollen Morphology and Its Relationship to Taxonomy of the Genus Sarracenia (Sarraceniaceae)
inferredcites →https://doi.org/10.3372/wi.39.39201openalex-snapshot
Caryophyllales phylogenetics: disentangling Phytolaccaceae and Molluginaceae and description of Microteaceae as a new isolated family
inferredcites →https://doi.org/10.3372/wi.45.45301openalex-snapshot
A taxonomic backbone for the global synthesis of species diversity in the angiosperm order Caryophyllales
inferredcites →https://doi.org/10.3417/2012047openalex-snapshot
Evolution of Angiosperm Pollen. 1. Introduction1
inferredcites →https://doi.org/10.3417/2012048openalex-snapshot
Evolution of Angiosperm Pollen. 2. The Basal Angiosperms1
inferredcites →https://doi.org/10.3417/2014014openalex-snapshot
Evolution of Angiosperm Pollen. 3. Monocots1
inferredcites →https://doi.org/10.3417/2015035openalex-snapshot
Evolution of Angiosperm Pollen: 4. Basal Eudicots
inferredcites →https://doi.org/10.3732/ajb.0800085openalex-snapshot
Evolutionary relationships in the showy mistletoe family (Loranthaceae)
inferredcites →https://doi.org/10.3732/ajb.0900346openalex-snapshot
The age and diversification of the angiosperms re‐revisited
inferredcites →https://doi.org/10.3732/ajb.1000022openalex-snapshot
Placing the woody tropical genera of Polygonaceae: A hypothesis of character evolution and phylogeny
inferredcites →https://doi.org/10.3732/ajb.1000404openalex-snapshot
Angiosperm phylogeny: 17 genes, 640 taxa
inferredcites →https://doi.org/10.3732/ajb.89.1.132openalex-snapshot
Molecular phylogenetics of Caryophyllales based on nuclear 18S rDNA and plastid rbcL, atpB, and matK DNA sequences
inferredcites →https://doi.org/10.3732/ajb.89.10.1670openalex-snapshot
Phylogeny of seed plants based on evidence from eight genes
inferredcites →https://doi.org/10.3732/ajb.89.4.677openalex-snapshot
Phylogenetic relationships in the order Ericales s.l.: analyses of molecular data from five genes from the plastid and mitochondrial genomes
inferredcites →https://doi.org/10.3732/ajb.90.1.123openalex-snapshot
Phylogeny of the sundews, Drosera (Droseraceae), based on chloroplast rbcL and nuclear 18S ribosomal DNA Sequences
inferredcites →https://doi.org/10.3732/ajb.90.12.1758openalex-snapshot
Angiosperm phylogeny based on <011>mat K sequence information
inferredcites →https://doi.org/10.3732/ajb.90.3.461openalex-snapshot
Gunnerales are sister to other core eudicots: implications for the evolution of pentamery
inferredcites →https://doi.org/10.3732/ajb.90.9.1357openalex-snapshot
Phylogenetic analyses of Cornales based on 26S rRNA and combined 26S rDNA‐MATK‐RBCL sequence data
inferredcites →https://doi.org/10.3732/ajb.93.3.399openalex-snapshot
Molecular phylogeny of the Caryophyllaceae (Caryophyllales) inferred from chloroplast matK and nuclear rDNA ITS sequences
inferredcites →https://doi.org/10.3732/ajb.94.1.89openalex-snapshot
The closest relatives of cacti: insights from phylogenetic analyses of chloroplast and mitochondrial sequences with special emphasis on relationships in the tribe Anacampseroteae
inferredcites →https://doi.org/10.3897/phytokeys.31.6251openalex-snapshot
A taxonomic synopsis of Altingiaceae with nine new combinations
inferredcites →https://doi.org/10.5281/zenodo.16192759openalex-snapshot
Pollen Morphology of Caryophyllaceae in Jordan
inferredcites →https://doi.org/10.54991/jop.1996.1228openalex-snapshot
LM and SEM Pollen Studies in Indian Alangiaceae
inferredcites →https://doi.org/10.6165/tai.2003.48(3).147openalex-snapshot
Comparative Study of the Pollen Wall Development in Illicium floridanum (Illiciaceae) and Schisandra chinensis (Schisandraceae)
inferredcites →https://doi.org/10.7751/telopea20065734openalex-snapshot
Pollen morphology of some rainforest taxa occurring in the Illawarra region of New South Wales, Australia
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.5091/plecevo.102524zenodo-depositor-declared
Evolution of pollen grain morphology in Amorimia and allies evidences the importance of palynological apomorphies and homoplasies in Malpighiaceae systematics
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/s10722-024-01939-yopenalex-snapshot
Molecular, morphological, palynological and biochemical characterization of six accessions of two Mangifera indica L cultivars (Keitt and Ewais) native to Egypt
inferred← citeshttps://doi.org/10.1007/s11756-025-01993-6openalex-snapshot
Exploring the palynology of Coleus Lour. (Lamiaceae) from an evolutionary perspective
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/s12594-023-2268-2openalex-snapshot
Fossil Mahogany from the Early Paleogene of India
inferred← citeshttps://doi.org/10.1016/j.ympev.2018.12.023openalex-snapshot
Plastid phylogenomic insights into the evolution of Caryophyllales
inferred← citeshttps://doi.org/10.1093/aob/mcaf213openalex-snapshot
Morphological innovation and lineage-specific history drive disparification in the aggregated pollen of mimosoid plants
inferred← citeshttps://doi.org/10.1093/botlinnean/boab025openalex-snapshot
Fossil pollen from early Palaeogene sediments in western India provides phylogenetic insights into divergence history and pollen character evolution in the pantropical family Ebenaceae
inferred← citeshttps://doi.org/10.15421/012415openalex-snapshot
Palynological data on the genus Cornus (Cornaceae)
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/10.3417/2020500openalex-snapshot
Evolution of Angiosperm Pollen: 8. Lamiids
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