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Phylogenetic assessment of pollen characters in Myrtaceae

https://doi.org/10.1071/sb11019
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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/tax.593007openalex-snapshot
Melaleuca revisited: cpDNA and morphological data confirm that Melaleuca L. (Myrtaceae) is not monophyletic
inferredcites →https://doi.org/10.1007/978-3-642-39417-1openalex-snapshot
Flowering plants, Eudicots : Malpighiales
inferredcites →https://doi.org/10.1007/s00606-004-0162-yopenalex-snapshot
Relationships within Myrtaceae sensu lato based on a matK phylogeny
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/s00606-009-0259-4openalex-snapshot
Pollen evolution and its taxonomic significance in Cuscuta (dodders, Convolvulaceae)
inferredcites →https://doi.org/10.1016/0034-6667(95)00076-3openalex-snapshot
Late-glacial palynology of the Myrtaceae of southern Chile
inferredcites →https://doi.org/10.1016/0034-6667(95)00113-1openalex-snapshot
Neogene environments in Australia, 1: re-evaluation of microfloras associated with important Early Pliocene marsupial remains at Grange Burn, southwest Victoria
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.2008.12.009openalex-snapshot
Pollen morphology of Gaultheria L. and related genera of subfamily Vaccinioideae: Taxonomic and evolutionary significance
inferredcites →https://doi.org/10.1016/j.revpalbo.2012.03.003openalex-snapshot
Fossil myrtaceous pollen as evidence for the evolutionary history of Myrtaceae: A review of fossil Myrtaceidites species
inferredcites →https://doi.org/10.1016/j.tree.2004.11.010openalex-snapshot
Do early branching lineages signify ancestral traits?
inferredcites →https://doi.org/10.1016/j.ympev.2006.08.013openalex-snapshot
Structural partitioning, paired-sites models and evolution of the ITS transcript in Syzygium and Myrtaceae
inferredcites →https://doi.org/10.1016/j.ympev.2008.12.013openalex-snapshot
Using fossils and molecular data to reveal the origins of the Cape proteas (subfamily Proteoideae)
inferredcites →https://doi.org/10.1016/j.ympev.2009.05.015openalex-snapshot
Dating the evolutionary origins of wrasse lineages (Labridae) and the rise of trophic novelty on coral reefs
inferredcites →https://doi.org/10.1016/j.ympev.2011.12.003openalex-snapshot
Are pollen fossils useful for calibrating relaxed molecular clock dating of phylogenies? A comparative study using Myrtaceae
inferredcites →https://doi.org/10.1016/s0034-6667(97)00028-6openalex-snapshot
Eucalyptus (Myrtaceae) pollen and its potential role in investigations of Holocene environments in southwestern Australia
inferredcites →https://doi.org/10.1016/s0140-1963(18)31779-8openalex-snapshot
Cahiers de Micropaléontologie
inferredcites →https://doi.org/10.1016/s0169-5347(98)01382-2openalex-snapshot
Reconstructing ancestral character states: a critical reappraisal
inferredcites →https://doi.org/10.1016/s0254-6299(16)31645-3openalex-snapshot
The genus Eugenia (Myrtaceae) in southern Africa: Morphology and taxonomic value of pollen
inferredcites →https://doi.org/10.1017/s0094837300015840openalex-snapshot
Phylogenies and angiosperm diversification
inferredcites →https://doi.org/10.1071/bt11174openalex-snapshot
Pollen morphology of the Myrtaceae. Part 1: tribes Eucalypteae, Lophostemoneae, Syncarpieae, Xanthostemoneae and subfamily Psiloxyloideae
inferredcites →https://doi.org/10.1071/bt11175openalex-snapshot
Pollen morphology of the Myrtaceae. Part 2: tribes Backhousieae, Melaleuceae, Metrosidereae, Osbornieae and Syzygieae
inferredcites →https://doi.org/10.1071/bt11176openalex-snapshot
Pollen morphology of the Myrtaceae. Part 3: tribes Chamelaucieae, Leptospermeae and Lindsayomyrteae
inferredcites →https://doi.org/10.1071/bt11177openalex-snapshot
Pollen morphology of the Myrtaceae. Part 4: tribes Kanieae, Myrteae and Tristanieae
inferredcites →https://doi.org/10.1071/bt9560013openalex-snapshot
Pollen morphology of Myrtaceae from the south-west Pacific area
inferredcites →https://doi.org/10.1071/bt9810159openalex-snapshot
Pollen Morphology in the Subtribe Metrosiderinae of the Leptospermoideae (Myrtaceae) and Its Taxonomic Significance.
inferredcites →https://doi.org/10.1071/bt9820075openalex-snapshot
Exine Ultrastructure of Myrtaceous Pollen
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/10.1080/01916122.1999.9989528openalex-snapshot
Palynostratigraphy of the murray basin, inland Southeastern Australia
inferredcites →https://doi.org/10.1080/10635150701491156openalex-snapshot
Assessing Calibration Uncertainty in Molecular Dating: The Assignment of Fossils to Alternative Calibration Points
inferredcites →https://doi.org/10.1086/375424openalex-snapshot
Pollen Diversity and Evolution in Myristicaceae (Magnoliales)
inferredcites →https://doi.org/10.1086/421066openalex-snapshot
Clades, Clocks, and Continents: Historical and Biogeographical Analysis of Myrtaceae, Vochysiaceae, and Relatives in the Southern Hemisphere
inferredcites →https://doi.org/10.1093/aob/mcq088openalex-snapshot
Evolution of exceptional species richness among lineages of fleshy-fruited Myrtaceae
inferredcites →https://doi.org/10.1111/j.0014-3820.2000.tb01254.xopenalex-snapshot
RECONSTRUCTING PLUMAGE EVOLUTION IN ORIOLES (ICTERUS): REPEATED CONVERGENCE AND REVERSAL IN PATTERNS
inferredcites →https://doi.org/10.1111/j.0307-6970.2004.00262.xopenalex-snapshot
Which side of the tree is more basal?
inferredcites →https://doi.org/10.1111/j.1095-8312.2004.00396.xopenalex-snapshot
The gall-inducing habit has evolved multiple times among the eriococcid scale insects (Sternorrhyncha: Coccoidea: Eriococcidae)
inferredcites →https://doi.org/10.1111/j.1095-8339.2008.00781.xopenalex-snapshot
Pollen morphology and systematics of palaeotropicalPhyllanthusand related genera of subtribe Phyllanthinae (Euphorbiaceae)
inferredcites →https://doi.org/10.1111/j.1096-0031.1993.tb00226.xopenalex-snapshot
THE HOLY GRAIL OF THE PERFECT CHARACTER: THE CLADISTIC TREATMENT OF MORPHOMETRIC DATA
inferredcites →https://doi.org/10.1111/j.1096-0031.1998.tb00335.xopenalex-snapshot
The Logical Basis for the use of Continuous Characters in Phylogenetic Systematics
inferredcites →https://doi.org/10.1111/j.1096-0031.2006.00122.xopenalex-snapshot
Continuous characters analyzed as such
inferredcites →https://doi.org/10.1111/j.1096-0031.2007.00175.xopenalex-snapshot
Ribosomal DNA pseudogenes are widespread in the eucalypt group (Myrtaceae): implications for phylogenetic analysis
inferredcites →https://doi.org/10.1111/j.1365-2699.2007.01749.xopenalex-snapshot
Molecular dating of the ‘Gondwanan’ plant family Proteaceae is only partially congruent with the timing of the break‐up of Gondwana
inferredcites →https://doi.org/10.1590/s0074-02761972000400002openalex-snapshot
Catálogo sistemático dos pólens das plantas arbóreas do Brasil meridional XV - Myrtaceae
inferredcites →https://doi.org/10.1663/0006-8101(2005)071[0354:pcatps]2.0.co;2openalex-snapshot
Palynological Characters and Their Phylogenetic Signal in Rubiaceae
inferredcites →https://doi.org/10.2307/1484763openalex-snapshot
Palynology of the Pedawan and Plateau Sandstone Formations (Cretaceous-Eocene) in Sarawak, Malaysia
inferredcites →https://doi.org/10.2307/2399159openalex-snapshot
Myrtales and Myrtaceae-A Phylogenetic Analysis
inferredcites →https://doi.org/10.2307/2399170openalex-snapshot
Pollen Characters in Relation to the Delimitation of Myrtales
inferredcites →https://doi.org/10.2307/2419343openalex-snapshot
Character States, Morphological Variation, and Phylogenetic Analysis: A Review
inferredcites →https://doi.org/10.3732/ajb.91.10.1666openalex-snapshot
Fossil evidence and phylogeny: the age of major angiosperm clades based on mesofossil and macrofossil evidence from Cretaceous deposits
inferredcites →https://doi.org/10.3767/000651903x675008openalex-snapshot
Pollen of Syzygium (Myrtaceae) from SE Asia, especially Thailand
inferredcites →https://doi.org/10.5860/choice.32-3881openalex-snapshot
Systematics and the fossil record: documenting evolutionary patterns

What points at this work

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

inferred← citeshttps://doi.org/10.1071/sb18015zenodo-depositor-declared
A dated molecular perspective of eucalypt taxonomy, evolution and diversification
inferred← citeshttps://doi.org/10.1071/sb21032zenodo-depositor-declared
Three new tribes in Myrtaceae and reassessment of Kanieae
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/10.1002/ajb2.1790openalex-snapshot
Phylogenomics and continental biogeographic disjunctions: insight from the Australian starflowers (Calytrix)
inferred← citeshttps://doi.org/10.1002/ece3.7679openalex-snapshot
Pollen DNA metabarcoding identifies regional provenance and high plant diversity in Australian honey
inferred← citeshttps://doi.org/10.1002/jemt.23742openalex-snapshot
Scanning electron imaging of mellitophilous and allergenic pollen grain of arid and northern irrigated agroecological zones of Pakistan
inferred← citeshttps://doi.org/10.1007/s00606-016-1373-8openalex-snapshot
Taxonomic significance of pollen morphology for species delimitation in Psidium (Myrtaceae)
inferred← citeshttps://doi.org/10.1007/s11101-013-9331-3openalex-snapshot
The evolution of foliar terpene diversity in Myrtaceae
inferred← citeshttps://doi.org/10.1016/j.jasrep.2018.06.039openalex-snapshot
Pollen evidence of medicine from an embalming jar associated with Vittoria della Rovere, Florence, Italy
inferred← citeshttps://doi.org/10.1016/j.jop.2026.100343openalex-snapshot
Miocene Syzygium Gaertn. (Myrtaceae) from India and its ancestral lineages from Gondwanaland
inferred← citeshttps://doi.org/10.1016/j.ympev.2011.12.003openalex-snapshot
Are pollen fossils useful for calibrating relaxed molecular clock dating of phylogenies? A comparative study using Myrtaceae
inferred← citeshttps://doi.org/10.1016/j.ympev.2015.07.007openalex-snapshot
Interpreting the modern distribution of Myrtaceae using a dated molecular phylogeny
inferred← citeshttps://doi.org/10.1017/9781316339701.002openalex-snapshot
Ecological Processes
inferred← citeshttps://doi.org/10.1017/9781316339701.004openalex-snapshot
Evolutionary Biogeography of the Australian Flora in the Cenozoic Era
inferred← citeshttps://doi.org/10.1071/bt16124openalex-snapshot
How old are the eucalypts? A review of the microfossil and phylogenetic evidence
inferred← citeshttps://doi.org/10.1080/14772019.2020.1863488openalex-snapshot
New pollen genera and species from the Oligocene of northern Spain and a systematic, biostratigraphic and biogeographic re-evaluation of coeval taxa
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/10.1111/jse.13047openalex-snapshot
Perianth evolution and implications for generic delimitation in the eucalypts (Myrtaceae), including the description of the new genus, Blakella
inferred← citeshttps://doi.org/10.1371/journal.pone.0187228openalex-snapshot
A continuous morphological approach to study the evolution of pollen in a phylogenetic context: An example with the order Myrtales
inferred← citeshttps://doi.org/10.1371/journal.pone.0197545openalex-snapshot
Pollen analysis of Australian honey
inferred← citeshttps://doi.org/10.1371/journal.pone.0218995openalex-snapshot
Identifying genetic markers for a range of phylogenetic utility–From species to family level
inferred← citeshttps://doi.org/10.1600/036364415x689249openalex-snapshot
An Expanded Metrosideros (Myrtaceae) to Include Carpolepis and Tepualia Based on Nuclear Genes
inferred← citeshttps://doi.org/10.3389/frbee.2025.1508958openalex-snapshot
Introduced honey bees (Apis mellifera) potentially reduce fitness of cavity-nesting native bees through a male-bias sex ratio, brood mortality and reduced reproduction
inferred← citeshttps://doi.org/10.4067/s0717-66432015000100010openalex-snapshot
Leaf micromorphology and anatomy of Myrceugenia rufa (Myrtaceae). An endemic coastal shrub of north-central Chile
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