On the public citation graph

A continuous morphological approach to study the evolution of pollen in a phylogenetic context: An example with the order Myrtales

https://doi.org/10.1371/journal.pone.0187228

0 signed · 189 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/bimj.200810425openalex-snapshot

Simultaneous Inference in General Parametric Models

inferredcites →https://doi.org/10.1002/j.1537-2197.1968.tb07473.xopenalex-snapshot

PALYNOLOGY AND SYSTEMATICS OF CUPHEA (LYTHRACEAE). I. MORPHOLOGY AND ULTRASTRUCTURE OF THE POLLEN WALL

inferredcites →https://doi.org/10.1002/j.1537-2197.1975.tb12334.xopenalex-snapshot

THE EVOLUTION OF POLLEN TETRADS IN ONAGRACEAE

inferredcites →https://doi.org/10.1002/j.1537-2197.1979.tb06256.xopenalex-snapshot

MORPHOMETRIC ANALYSIS OF POLLEN FROM FOUR SPECIES OF AMBROSIA (COMPOSITAE)

inferredcites →https://doi.org/10.1002/j.1537-2197.1983.tb06414.xopenalex-snapshot

HALF PSEUDOCOLPI, A UNIQUE FEATURE OF OLINIA (OLINIACEAE) POLLEN

inferredcites →https://doi.org/10.1002/j.1537-2197.1985.tb08346.xopenalex-snapshot

PALYNOLOGY AND SYSTEMATICS OF THE LYTHRACEAE. I. INTRODUCTION AND GENERA ADENARIA THROUGH GINORIA

inferredcites →https://doi.org/10.1002/j.1537-2197.1985.tb08348.xopenalex-snapshot

FUCHSIA POLLEN FROM THE EARLY MIOCENE OF NEW ZEALAND

inferredcites →https://doi.org/10.1002/j.1537-2197.1987.tb08687.xopenalex-snapshot

PALYNOLOGY AND SYSTEMATICS OF THE LYTHRACEAE. II. GENERA HAITIA THROUGH PEPLIS

inferredcites →https://doi.org/10.1002/j.1537-2197.1990.tb13543.xopenalex-snapshot

PALYNOLOGY AND SYSTEMATICS OF THE LYTHRACEAE. III. GENERA PHYSOCALYMMA THROUGH WOODFORDIA, ADDENDA, AND CONCLUSIONS

inferredcites →https://doi.org/10.1006/anbo.1998.0752openalex-snapshot

The role of Genomic Constraints upon Evolutionary Changes in Genome Size and Chromosome Organization

inferredcites →https://doi.org/10.1006/bijl.1998.0235openalex-snapshot

Pollen-size comparisons among animal-pollinated angiosperms with different pollination characteristics

inferredcites →https://doi.org/10.1006/bojl.1994.1040openalex-snapshot

Pollen presenters in the flowering plants-form and function

inferredcites →https://doi.org/10.1007/bf02931138openalex-snapshot

Discontinuous DNA variation in the evolution of plant species

inferredcites →https://doi.org/10.1007/s004970000030openalex-snapshot

Pollen size evolution: correlation between pollen volume and pistil length in Asteraceae

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/10.1007/s00606-011-0462-yopenalex-snapshot

Systematic importance of pollen morphological features of selected species from the genus Rosa (Rosaceae)

inferredcites →https://doi.org/10.1007/s00606-011-0578-0openalex-snapshot

Diverse fossil Onagraceae pollen from a Miocene palynoflora of north-east China: early steps in resolving the phytogeographic history of the family

inferredcites →https://doi.org/10.1007/s00606-013-0762-5openalex-snapshot

Intraspecific variability of pollen morphology as revealed by elliptic Fourier analysis

inferredcites →https://doi.org/10.1007/s00606-013-0832-8openalex-snapshot

Structural basis of harmomegathy: evidence from Boraginaceae pollen

inferredcites →https://doi.org/10.1016/0034-6667(67)90050-4openalex-snapshot

Pollen morphology of the Onagraceae

inferredcites →https://doi.org/10.1016/0034-6667(81)90013-0openalex-snapshot

Structure and function in angiosperm pollen wall evolution

inferredcites →https://doi.org/10.1016/0034-6667(81)90016-6openalex-snapshot

Exine architecture and function in some lythraceae and sonneratiaceae

inferredcites →https://doi.org/10.1016/0146-664x(82)90034-xopenalex-snapshot

Elliptic Fourier features of a closed contour

inferredcites →https://doi.org/10.1016/j.revpalbo.2004.03.005openalex-snapshot

The Miocene genus Fupingopollenites: comparisons with ultrastructure and pseudocolpi in modern pollen

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.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/j.ympev.2013.10.010openalex-snapshot

Adaptive radiation, correlated and contingent evolution, and net species diversification in Bromeliaceae

inferredcites →https://doi.org/10.1016/j.ympev.2015.07.007openalex-snapshot

Interpreting the modern distribution of Myrtaceae using a dated molecular phylogeny

inferredcites →https://doi.org/10.1016/j.ympev.2015.10.001openalex-snapshot

Divergence times, historical biogeography, and shifts in speciation rates of Myrtales

inferredcites →https://doi.org/10.1029/97jd03649openalex-snapshot

Latitudinal temperature gradients and climate change

inferredcites →https://doi.org/10.1038/nature07764openalex-snapshot

Phylogenetic biome conservatism on a global scale

inferredcites →https://doi.org/10.1038/ncomms2958openalex-snapshot

Rates of speciation and morphological evolution are correlated across the largest vertebrate radiation

inferredcites →https://doi.org/10.1038/nmeth.2089openalex-snapshot

NIH Image to ImageJ: 25 years of image analysis

inferredcites →https://doi.org/10.1038/nrg2829openalex-snapshot

Evolution and development of shape: integrating quantitative approaches

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/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/bt9910229openalex-snapshot

Secondary Pollen Presentation in the Chamelaucium Alliance of the Myrtaceae: a Compact Substigmatic Ring in Chamelaucium

inferredcites →https://doi.org/10.1071/bt9930511openalex-snapshot

Reproductive Biology of Australian Myrtaceae

inferredcites →https://doi.org/10.1071/sb11019openalex-snapshot

Phylogenetic assessment of pollen characters in Myrtaceae

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.1308932111openalex-snapshot

The latitudinal species richness gradient in New World woody angiosperms is consistent with the tropical conservatism hypothesis

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

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

inferredcites →https://doi.org/10.1080/00173130802457255openalex-snapshot

Lagerstroemia (Lythraceae) pollen from the Miocene of eastern China

inferredcites →https://doi.org/10.1080/00173139009429975openalex-snapshot

Harmomegathy in the Acanthaceae

inferredcites →https://doi.org/10.1080/00173139209430731openalex-snapshot

Notes on the exine ultrastructure of Onagraceae and Rhododendroideae (Ericaceae)

inferredcites →https://doi.org/10.1080/00173139709362602openalex-snapshot

Palynological studies in the family Melastomataceae from Thailand

inferredcites →https://doi.org/10.1080/0028825x.1979.10432572openalex-snapshot

A survey of reproductive biology in Onagraceae

inferredcites →https://doi.org/10.1080/106351501753328811openalex-snapshot

Character Analysis in Morphological Phylogenetics: Problems and Solutions

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/10.1086/426002openalex-snapshot

Phylogenetic Comparative Analysis: A Modeling Approach for Adaptive Evolution

inferredcites →https://doi.org/10.1086/590395openalex-snapshot

Morphometrics of the Avian Small Intestine Compared with That of Nonflying Mammals: A Phylogenetic Approach

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

Pollen Evolution in the Early‐Divergent Monocot Order Alismatales

inferredcites →https://doi.org/10.1086/663968openalex-snapshot

Morphological Trends in the Fossil Pollen ofDecodonand the Paleobiogeographic History of the Genus

inferredcites →https://doi.org/10.1086/667614openalex-snapshot

Pollen Evolution in the Clusioid Clade (Malpighiales)

inferredcites →https://doi.org/10.1093/bioinformatics/bts492openalex-snapshot

treePL: divergence time estimation using penalized likelihood for large phylogenies

inferredcites →https://doi.org/10.1093/bioinformatics/btu033openalex-snapshot

RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies

inferredcites →https://doi.org/10.1093/molbev/mst010openalex-snapshot

MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability

inferredcites →https://doi.org/10.1093/sysbio/syr107openalex-snapshot

Best Practices for Justifying Fossil Calibrations

inferredcites →https://doi.org/10.1093/sysbio/syr116openalex-snapshot

Testing the Impact of Calibration on Molecular Divergence Times Using a Fossil-Rich Group: The Case of Nothofagus (Fagales)

inferredcites →https://doi.org/10.1093/sysbio/syt002openalex-snapshot

Geometric Morphometric Character Suites as Phylogenetic Data: Extracting Phylogenetic Signal from Gastropod Shells

inferredcites →https://doi.org/10.1093/sysbio/syu005openalex-snapshot

A Linear-Time Algorithm for Gaussian and Non-Gaussian Trait Evolution Models

inferredcites →https://doi.org/10.1093/sysbio/syv043openalex-snapshot

Detecting Adaptive Evolution in Phylogenetic Comparative Analysis Using the Ornstein–Uhlenbeck Model

inferredcites →https://doi.org/10.1098/rsbl.2011.0356openalex-snapshot

Synthesizing and databasing fossil calibrations: divergence dating and beyond

inferredcites →https://doi.org/10.1098/rsbl.2014.0223openalex-snapshot

Eocene fossil is earliest evidence of flower-visiting by birds

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/10.1109/gce.2010.5676129openalex-snapshot

Creating the CIPRES Science Gateway for inference of large phylogenetic trees

inferredcites →https://doi.org/10.1111/1365-2745.12074openalex-snapshot

Latitudinal gradients as natural laboratories to infer species' responses to temperature

inferredcites →https://doi.org/10.1111/2041-210x.12285openalex-snapshot

Intrinsic inference difficulties for trait evolution with Ornstein‐Uhlenbeck models

inferredcites →https://doi.org/10.1111/2041-210x.12534openalex-snapshot

Fast and accurate detection of evolutionary shifts in Ornstein–Uhlenbeck models

inferredcites →https://doi.org/10.1111/bij.12297openalex-snapshot

Calibrated chronograms, fossils, outgroup relationships, and root priors: re-examining the historical biogeography of Geraniales

inferredcites →https://doi.org/10.1111/evo.12180openalex-snapshot

FRUIT EVOLUTION AND DIVERSIFICATION IN CAMPANULID ANGIOSPERMS

inferredcites →https://doi.org/10.1111/evo.12670openalex-snapshot

Integration and macroevolutionary patterns in the pollination biology of conifers

inferredcites →https://doi.org/10.1111/gbi.12023openalex-snapshot

Combining geometric morphometrics, molecular phylogeny, and micropaleontology to assess evolutionary patterns in M allomonas (Synurophyceae: Heterokontophyta)

inferredcites →https://doi.org/10.1111/geb.12326openalex-snapshot

Estimating species diversity and distribution in the era of B ig D ata: to what extent can we trust public databases?

inferredcites →https://doi.org/10.1111/j.0014-3820.2004.tb00472.xopenalex-snapshot

CALIBRATION OF MOLECULAR CLOCKS AND THE BIOGEOGRAPHIC HISTORY OF CRYPTERONIACEAE

inferredcites →https://doi.org/10.1111/j.0014-3820.2004.tb00473.xopenalex-snapshot

CALIBRATION OF MOLECULAR CLOCKS AND THE BIOGEOGRAPHIC HISTORY OF CRYPTERONIACEAE: A REPLY TO MOYLE

inferredcites →https://doi.org/10.1111/j.1095-8312.2012.01910.xopenalex-snapshot

First Miocene fossils of Vivianiaceae shed new light on phylogeny, divergence times, and historical biogeography of Geraniales

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.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.1365-2699.2006.01645.xopenalex-snapshot

Introducing a new (freeware) tool for palynology

inferredcites →https://doi.org/10.1111/j.1420-9101.2011.02410.xopenalex-snapshot

Developmental plasticity, morphological variation and evolvability: a multilevel analysis of morphometric integration in the shape of compound leaves

inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02528.xopenalex-snapshot

Genome size is a strong predictor of cell size and stomatal density in angiosperms

inferredcites →https://doi.org/10.1111/j.1558-5646.1997.tb01457.xopenalex-snapshot

STABILIZING SELECTION AND THE COMPARATIVE ANALYSIS OF ADAPTATION

inferredcites →https://doi.org/10.1111/j.1558-5646.2012.01619.xopenalex-snapshot

MODELING STABILIZING SELECTION: EXPANDING THE ORNSTEIN-UHLENBECK MODEL OF ADAPTIVE EVOLUTION

inferredcites →https://doi.org/10.1111/j.2041-210x.2011.00169.xopenalex-snapshot

phytools: an R package for phylogenetic comparative biology (and other things)

inferredcites →https://doi.org/10.1111/j.2517-6161.1996.tb02080.xopenalex-snapshot

Regression Shrinkage and Selection Via the Lasso

inferredcites →https://doi.org/10.1111/jbi.12312openalex-snapshot

Disentangling the influence of climatic and geological changes on species radiations

inferredcites →https://doi.org/10.1111/nph.12969openalex-snapshot

The floral morphospace – a modern comparative approach to study angiosperm evolution

inferredcites →https://doi.org/10.1111/nph.13114openalex-snapshot

Green Web or megabiased clock? Plant fossils from Gondwanan Patagonia speak on evolutionary radiations

inferredcites →https://doi.org/10.1139/b83-256openalex-snapshot

Quantification of leaf shape with a microcomputer and Fourier transform

inferredcites →https://doi.org/10.1155/2010/171435openalex-snapshot

Small Heat Shock Protein Responses Differ between Chaparral Shrubs from Contrasting Microclimates

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

On the Relationship between Pollen Size and Genome Size

inferredcites →https://doi.org/10.1186/1471-2105-14-16openalex-snapshot

The taxonomic name resolution service: an online tool for automated standardization of plant names

inferredcites →https://doi.org/10.1186/1471-2105-14-s15-s14openalex-snapshot

Statistics for approximate gene clusters

inferredcites →https://doi.org/10.1360/aps050006openalex-snapshot

Additional notes on Melastomataceae of China

inferredcites →https://doi.org/10.1371/journal.pone.0025630openalex-snapshot

Leaf Morphology, Taxonomy and Geometric Morphometrics: A Simplified Protocol for Beginners

inferredcites →https://doi.org/10.1371/journal.pone.0098536openalex-snapshot

The Evolution of Morphospace in Phytophagous Scarab Chafers: No Competition - No Divergence?

inferredcites →https://doi.org/10.15517/rbt.v62i3.12323openalex-snapshot

Morfología del polen de las especies de árboles de Vochysiaceae en el estado de Santa Catarina, sur de Brasil

inferredcites →https://doi.org/10.1590/s0074-02761975000100007openalex-snapshot

Catálogo sistemático dos pólens das plantas arbóreas do Brasil Meridional: XX - Chloranthaceae e Piperaceae

inferredcites →https://doi.org/10.1590/s0100-84042006000400002openalex-snapshot

Polinização e dispersão de sementes em Myrtaceae do Brasil

inferredcites →https://doi.org/10.1590/s0102-33062009000300018openalex-snapshot

Stigmatic surface in the Vochysiaceae: reproductive and taxonomic implications

inferredcites →https://doi.org/10.1590/s2236-89062007000400008openalex-snapshot

Flora Polínica da Reserva do Parque Estadual das Fontes do Ipiranga (São Paulo, Brasil): Família: 90-Melastomataceae

inferredcites →https://doi.org/10.1600/036364405775097743openalex-snapshot

Pollen Evolution in Yams (Dioscorea: Dioscoreaceae)

inferredcites →https://doi.org/10.1600/036364408784571482openalex-snapshot

Phylogeny and Historical Biogeography of Geraniaceae in Relation to Climate Changes and Pollination Ecology

inferredcites →https://doi.org/10.18637/jss.v028.i08openalex-snapshot

Implementing a Class of Permutation Tests: The coin Package

inferredcites →https://doi.org/10.18637/jss.v056.i13openalex-snapshot

Momocs : Outline Analysis Using R

inferredcites →https://doi.org/10.1890/es11-00147.1openalex-snapshot

Does climate affect pollen morphology? Optimal size and shape of pollen grains under various desiccation intensity

inferredcites →https://doi.org/10.2307/2388870openalex-snapshot

The Breeding System and Pollinators of Melastoma affine (Melastomataceae); A Pioneer Shrub in Tropical Australia

inferredcites →https://doi.org/10.2307/2398913openalex-snapshot

Form and Function in Angiosperm Pollen

inferredcites →https://doi.org/10.2307/2399008openalex-snapshot

An Embryological Analysis of Myrtales: Its Definition and Characteristics

inferredcites →https://doi.org/10.2307/2399056openalex-snapshot

A Palynological Study of the Genus Fuchsia (Onagraceae)

inferredcites →https://doi.org/10.2307/2399158openalex-snapshot

The Order Myrtales: Circumscription, Variation, and Relationships

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/10.2307/2399497openalex-snapshot

A Survey of Reproductive Biology in Neotropical Melastomataceae and Memecylaceae

inferredcites →https://doi.org/10.2307/2418502openalex-snapshot

The American Species of Nesaea (Lythraceae) and Their Relationship to Heimia and Decodon

inferredcites →https://doi.org/10.2307/2419432openalex-snapshot

Interfamilial Relationships in Myrtales: Molecular Phylogeny and Patterns of Morphological Evolution

inferredcites →https://doi.org/10.2307/2440476openalex-snapshot

Palynology and Systematics of Cuphea (Lythraceae). I. Morphology and Ultrastructure of the Pollen Wall

inferredcites →https://doi.org/10.2307/2443255openalex-snapshot

Half Pseudocolpi, a Unique Feature of Olinia (Olinia (Oliniaceae) Pollen

inferredcites →https://doi.org/10.2307/2443864openalex-snapshot

Palynology and Systematics of the Lythraceae. II. Genera haitia Through Peplis

inferredcites →https://doi.org/10.2307/25065308openalex-snapshot

Viscin threads on pollen of Circaea × intermedia Ehrh. (Circaeeae: Onagraceae)

inferredcites →https://doi.org/10.2307/2806163openalex-snapshot

Rodent Pollination of Blakea (Melastomataceae) in a Costa Rican Cloud Forest

inferredcites →https://doi.org/10.2307/2807100openalex-snapshot

Stanmarkia, a New Genus of Melastomataceae from the Volcanic Highlands of Western Guatemala and Adjacent Mexico

inferredcites →https://doi.org/10.2307/4110533openalex-snapshot

Systematic Studies in the Melastomataceae: Bellucia, Loreya and Macairea. Memoirs of the New York Botanical Garden Vol. 50

inferredcites →https://doi.org/10.2307/4129971openalex-snapshot

Pollen and Spores. Form and Function

inferredcites →https://doi.org/10.3417/2007028openalex-snapshot

Revision of the Caribbean Genus Ginoria (Lythraceae), Including Haitia From Hispaniola1

inferredcites →https://doi.org/10.3417/2007176openalex-snapshot

A Renaissance of Cytogenetics: Studies in Polyploidy and Chromosomal Evolution1

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

Angiosperm phylogeny: 17 genes, 640 taxa

inferredcites →https://doi.org/10.3732/ajb.1200416openalex-snapshot

Land plant evolutionary timeline: Gene effects are secondary to fossil constraints in relaxed clock estimation of age and substitution rates

inferredcites →https://doi.org/10.3732/ajb.1500394openalex-snapshot

Shape analysis of moss (Bryophyta) sporophytes: Insights into land plant evolution

inferredcites →https://doi.org/10.3732/ajb.89.9.1459openalex-snapshot

Morphometric analysis of pollen grains for paleoecological studies: classification of Picea from eastern North America

inferredcites →https://doi.org/10.5281/zenodo.59793openalex-snapshot

Morphocode: Coding Quantitative Data For Phylogenetic Analysis

inferredcites →https://doi.org/10.5586/asbp.2005.038openalex-snapshot

Pollen morphology of Rosa gallica L. (Rosaceae) from Southern Poland

inferredcites →https://doi.org/10.5897/ajps.9000236openalex-snapshot

Studies on the pollen biology of Terminalia paniculata Roth. (Combretaceae)

inferredcites →https://doi.org/10.6165/tai.2002.47(2).129openalex-snapshot

Pollen Flora of Yuenyang Lake Nature Preserve, Taiwan (IV)

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/10.1002/ajb2.1268openalex-snapshot

Tracking temporal shifts in area, biomes, and pollinators in the radiation of Salvia (sages) across continents: leveraging anchored hybrid enrichment and targeted sequence data

inferred← citeshttps://doi.org/10.1002/ajb2.1699openalex-snapshot

A nuclear phylogenomic study of the angiosperm order Myrtales, exploring the potential and limitations of the universal Angiosperms353 probe set

inferred← citeshttps://doi.org/10.1002/ajb2.70149openalex-snapshot

Flowers occupy color‐space extremes: an anthocyanin‐derived theoretical floral color‐space approach

inferred← citeshttps://doi.org/10.1002/cyto.a.24932openalex-snapshot

Multispectral Imaging Flow Cytometry for Spatio‐Temporal Pollen Trait Variation Measurements of Insect‐Pollinated Plants

inferred← citeshttps://doi.org/10.1002/fedr.202100052openalex-snapshot

Palynological study of the family Lythraceae J.St.‐Hil. in Iran; with special emphasis on the genera Ammannia, Lythrum, and Rotala

inferred← citeshttps://doi.org/10.1007/s00606-018-1559-3openalex-snapshot

Pollen morphology in natural diploid–polyploid hybridogeneous complex of the genus Onosma (Boraginaceae–Lithospermeae)

inferred← citeshttps://doi.org/10.1007/s00606-025-01955-0openalex-snapshot

Seed and pollen disparity and speciation in the genus Epilobium of the Onagraceae family

inferred← citeshttps://doi.org/10.1007/s00709-021-01671-9openalex-snapshot

Light and electron microscopies reveal unknown details of the pollen grain structure and physiology from Brazilian Cerrado species

inferred← citeshttps://doi.org/10.1007/s10142-025-01752-5openalex-snapshot

Sequence dynamics and plastome evolution: decoding the complete chloroplast genome of Oenothera drummondii and comparative analysis within Oenothera (Onagraceae)

inferred← citeshttps://doi.org/10.1007/s10722-024-02094-0openalex-snapshot

Pollen morphology and variability among Indian cultivars of Chrysanthemum morifolium and comparative analysis with genera of the Asteraceae family

inferred← citeshttps://doi.org/10.1007/s10722-024-02260-4openalex-snapshot

Heteromorphy in pollen grains of the tropical and subtropical selected Fabaceae species

inferred← citeshttps://doi.org/10.1007/s40415-024-01033-8openalex-snapshot

More of almost the same: novel pollen descriptions uncover subtle morphological variation in Mimosa L. (Leguminosae, Mimoseae)

inferred← citeshttps://doi.org/10.1007/s40415-024-01059-yopenalex-snapshot

Pollen evolution in the Stryphnodendron clade (Leguminosae, Mimoseae)

inferred← citeshttps://doi.org/10.1016/j.indcrop.2021.114321openalex-snapshot

Taxonomic and evolutionary impacts of anatomical and morphological characters in the genus Epilobium L. (Onagraceae)

inferred← citeshttps://doi.org/10.1016/j.ppees.2020.125556openalex-snapshot

Structure and evolution of polysporangiate anthers in Melastomataceae

inferred← citeshttps://doi.org/10.1016/j.revpalbo.2020.104273openalex-snapshot

Myrtaceae pollen morphology study from Bass Strait islands, Australia, is effective in separating region-specific fossil Myrtaceae pollen types

inferred← citeshttps://doi.org/10.1016/j.revpalbo.2020.104288openalex-snapshot

Three Aquilapollenites species from the late Maastrichtian of China: New data and comparisons

inferred← citeshttps://doi.org/10.1073/pnas.2007324117openalex-snapshot

Improving the taxonomy of fossil pollen using convolutional neural networks and superresolution microscopy

inferred← citeshttps://doi.org/10.1080/23766808.2021.1906138openalex-snapshot

Geometry morphometrics of plant structures as a phenotypic tool to differentiate Polylepis incana Kunth. and Polylepis racemosa Ruiz & Pav. reforested jointly in Ecuador

inferred← citeshttps://doi.org/10.1080/23802359.2018.1463828openalex-snapshot

The first complete chloroplast genome of a major mangrove species Sonneratia alba Sm. and its implications on conservation efforts

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/boac021openalex-snapshot

Recurrent evolutionary changes in pollen shape and ornamentation of the vataireoid clade (Papilionoideae, Fabaceae), an early-branching lineage of florally divergent genera

inferred← citeshttps://doi.org/10.1093/botlinnean/boae068openalex-snapshot

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

inferred← citeshttps://doi.org/10.1093/botlinnean/boaf052openalex-snapshot

Investigating palynotaxonomy and evolutionary trends in Cryptangieae (Cyperaceae)

inferred← citeshttps://doi.org/10.1111/btp.12847openalex-snapshot

Phylogenetic and ecological correlates of pollen morphological diversity in a Neotropical rainforest

inferred← citeshttps://doi.org/10.1111/cla.12488openalex-snapshot

Parsing a plethora of pollen: the role of pollen size and shape in the evolution of Boraginaceae

inferred← citeshttps://doi.org/10.1111/evo.14030openalex-snapshot

Pollinator shifts, contingent evolution, and evolutionary constraint drive floral disparity in Salvia (Lamiaceae): Evidence from morphometrics and phylogenetic comparative methods

inferred← citeshttps://doi.org/10.1111/jipb.70011openalex-snapshot

Genome duplications, genomic conflict, and rapid phenotypic evolution characterize the Cretaceous radiation of Fagales

inferred← citeshttps://doi.org/10.1111/nph.18024openalex-snapshot

Why does pollen morphology vary? Evolutionary dynamics and morphospace occupation in the largest angiosperm order (Asterales)

inferred← citeshttps://doi.org/10.1111/nph.19186openalex-snapshot

Deductive automated pollen classification in environmental samples via exploratory deep learning and imaging flow cytometry

inferred← citeshttps://doi.org/10.1111/nph.70250openalex-snapshot

Pollen morphology, deep learning, phylogenetics, and the evolution of environmental adaptations in Podocarpus

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

Climate adaptation and functional constraints drive pollen evolution in Apiales

inferred← citeshttps://doi.org/10.1186/s13717-020-00262-5openalex-snapshot

Staying alive on an active volcano: 80 years population dynamics of Cytisus aeolicus (Fabaceae) from Stromboli (Aeolian Islands, Italy)

inferred← citeshttps://doi.org/10.13057/biodiv/d230930openalex-snapshot

Pollen morphological characters variation among species of Strobilanthes s.l. from Sumatra, Indonesia and its taxonomic implications

inferred← citeshttps://doi.org/10.1371/journal.pbio.3000020openalex-snapshot

Birds, blooms, and evolving diversity

inferred← citeshttps://doi.org/10.1371/journal.pone.0272580openalex-snapshot

Pollen preferences of stingless bees in the Amazon region and southern highlands of Ecuador by scanning electron microscopy and morphometry

inferred← citeshttps://doi.org/10.21608/taec.2022.258213openalex-snapshot

Pollen grain diversity and application in taxonomy and evolution

inferred← citeshttps://doi.org/10.32859/era.25.8.1-21openalex-snapshot

Molecular and morphological analyses of plants with ethnomedicinal uses in northeastern Peru

inferred← citeshttps://doi.org/10.3389/fpls.2025.1558995openalex-snapshot

Systematic analysis of some Astereae (Asteraceae) species by Integrating pollen morphology and molecular evidence

inferred← citeshttps://doi.org/10.3390/ijms25137283openalex-snapshot

De Novo Hybrid Assembly Unveils Multi-Chromosomal Mitochondrial Genomes in Ludwigia Species, Highlighting Genomic Recombination, Gene Transfer, and RNA Editing Events

inferred← citeshttps://doi.org/10.3390/toxins11110637openalex-snapshot

Hadrurid Scorpion Toxins: Evolutionary Conservation and Selective Pressures

inferred← citeshttps://doi.org/10.3897/phytokeys.128.35842openalex-snapshot

Systematic relevance of pollen morphology in tribe Hylocereeae (Cactaceae)

inferred← citeshttps://doi.org/10.52547/ismj.24.2.111openalex-snapshot

Conocarpus Tree the Marine-Medicinal Treasure of Southern Iran: A Review of Botani-cal, Phytochemical and Medicinal Properties

inferred← citeshttps://doi.org/10.6084/m9.figshare.13226086openalex-snapshot

Additional file 1 of Staying alive on an active volcano: 80 years population dynamics of Cytisus aeolicus (Fabaceae) from Stromboli (Aeolian Islands, Italy)

inferred← citeshttps://doi.org/10.6084/m9.figshare.13226089openalex-snapshot

Additional file 2 of Staying alive on an active volcano: 80 years population dynamics of Cytisus aeolicus (Fabaceae) from Stromboli (Aeolian Islands, Italy)

inferred← citeshttps://doi.org/10.6084/m9.figshare.13226092openalex-snapshot

Additional file 3 of Staying alive on an active volcano: 80 years population dynamics of Cytisus aeolicus (Fabaceae) from Stromboli (Aeolian Islands, Italy)

inferred← citeshttps://doi.org/10.6084/m9.figshare.13226095openalex-snapshot

Additional file 4 of Staying alive on an active volcano: 80 years population dynamics of Cytisus aeolicus (Fabaceae) from Stromboli (Aeolian Islands, Italy)

inferred← citeshttps://doi.org/10.6084/m9.figshare.13226098openalex-snapshot

Additional file 5 of Staying alive on an active volcano: 80 years population dynamics of Cytisus aeolicus (Fabaceae) from Stromboli (Aeolian Islands, Italy)

inferred← citeshttps://doi.org/10.7717/peerj.5055openalex-snapshot

A novel approach to study the morphology and chemistry of pollen in a phylogenetic context, applied to the halophytic taxon Nitraria L.(Nitrariaceae)

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.