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Genome size evolution in Ontario ferns (Polypodiidae): evolutionary correlations with cell size, spore size, and habitat type and an absence of genome downsizing

https://doi.org/10.1139/gen-2014-0090
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What this work says

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

inferredcites →https://doi.org/10.1002/j.1537-2197.1953.tb06523.xopenalex-snapshot
CHROMOSOME STUDIES ON FERNS
inferredcites →https://doi.org/10.1002/j.1537-2197.1989.tb15057.xopenalex-snapshot
DROUGHT STRESS RESPONSES OF MICROSERIS SPECIES DIFFERING IN NUCLEAR DNA CONTENT
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Estimates of Nuclear DNA Content in Bryophyte Sperm Cells: Phylogenetic Considerations
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IOPB CHROMOSOME NUMBER REPORTS LIII
inferredcites →https://doi.org/10.1002/tax.613003openalex-snapshot
A revised family–level classification for eupolypod II ferns (Polypodiidae: Polypodiales)
inferredcites →https://doi.org/10.1006/bcmd.2001.0457openalex-snapshot
The Bigger the C-Value, the Larger the Cell: Genome Size and Red Blood Cell Size in Vertebrates
inferredcites →https://doi.org/10.1006/tpbi.2002.1605openalex-snapshot
Mutational Equilibrium Model of Genome Size Evolution
inferredcites →https://doi.org/10.1007/978-1-4613-8991-0openalex-snapshot
Spores of the Pteridophyta
inferredcites →https://doi.org/10.1007/bf02907241openalex-snapshot
Analysis of Nuclear DNA content in plant cells by Flow cytometry
inferredcites →https://doi.org/10.1007/s10577-011-9228-1openalex-snapshot
DNA content variation in monilophytes and lycophytes: large genomes that are not endopolyploid
inferredcites →https://doi.org/10.1007/s10577-011-9229-0openalex-snapshot
Co-evolution between transposable elements and their hosts: a major factor in genome size evolution?
inferredcites →https://doi.org/10.1016/b978-012301463-4/50013-9openalex-snapshot
Macroevolution and the Genome
inferredcites →https://doi.org/10.1016/j.gene.2003.09.030openalex-snapshot
Insertion–deletion biases and the evolution of genome size
inferredcites →https://doi.org/10.1016/j.plantsci.2008.03.015openalex-snapshot
Repeated big bangs and the expanding universe: Directionality in plant genome size evolution
inferredcites →https://doi.org/10.1016/j.tig.2003.09.010openalex-snapshot
Selfish DNA is maladaptive: evidence from the plant Red List
inferredcites →https://doi.org/10.1016/j.ympev.2011.03.010openalex-snapshot
First insights into fern matK phylogeny
inferredcites →https://doi.org/10.1016/s0074-7696(00)96004-2openalex-snapshot
Some aspects of plant karyology and karyosystematics
inferredcites →https://doi.org/10.1017/cbo9780511541827.008openalex-snapshot
Evolution of the nuclear genome of ferns and lycophytes
inferredcites →https://doi.org/10.1017/s1464793100005595openalex-snapshot
Coincidence, coevolution, or causation? DNA content, cell size, and the C-value enigma
inferredcites →https://doi.org/10.1023/a:1016015913350openalex-snapshot
Mechanisms and rates of genome expansion and contraction in flowering plants
inferredcites →https://doi.org/10.1023/a:1016020030189openalex-snapshot
Feast and famine in plant genomes
inferredcites →https://doi.org/10.1038/44766openalex-snapshot
Inferring the historical patterns of biological evolution
inferredcites →https://doi.org/10.1038/nature01843openalex-snapshot
The role of stomata in sensing and driving environmental change
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Endopolyploidy in seed plants is differently correlated to systematics, organ, life strategy and genome size
inferredcites →https://doi.org/10.1046/j.1461-0248.2002.00283.xopenalex-snapshot
Variation in nuclear DNA content across environmental gradients: a quantile regression analysis
inferredcites →https://doi.org/10.1071/pp00157openalex-snapshot
Leaf anatomical characteristics associated with shoot hydraulic conductance, stomatal conductance and stomatal sensitivity to changes of leaf water status in temperate deciduous trees
inferredcites →https://doi.org/10.1073/pnas.0811575106openalex-snapshot
The frequency of polyploid speciation in vascular plants
inferredcites →https://doi.org/10.1073/pnas.0904339106openalex-snapshot
Rapid DNA loss as a counterbalance to genome expansion through retrotransposon proliferation in plants
inferredcites →https://doi.org/10.1073/pnas.0905845106openalex-snapshot
A DNA barcode for land plants
inferredcites →https://doi.org/10.1073/pnas.49.6.897openalex-snapshot
A RELATIONSHIP BETWEEN DNA CONTENT, NUCLEAR VOLUME, AND MINIMUM MITOTIC CYCLE TIME
inferredcites →https://doi.org/10.1073/pnas.83.12.4389openalex-snapshot
Genetic evidence suggests that homosporous ferns with high chromosome numbers are diploid
inferredcites →https://doi.org/10.1085/jgp.34.4.451openalex-snapshot
THE DESOXYRIBONUCLEIC ACID CONTENT OF ANIMAL CELLS AND ITS EVOLUTIONARY SIGNIFICANCE
inferredcites →https://doi.org/10.1086/284706openalex-snapshot
Polyploidy and Breeding Systems in Homosporous Pteridophyta: A Reevaluation
inferredcites →https://doi.org/10.1086/286013openalex-snapshot
Phylogenies and the Comparative Method: A General Approach to Incorporating Phylogenetic Information into the Analysis of Interspecific Data
inferredcites →https://doi.org/10.1086/303327openalex-snapshot
Using the Past to Predict the Present: Confidence Intervals for Regression Equations in Phylogenetic Comparative Methods
inferredcites →https://doi.org/10.1086/343873openalex-snapshot
Phylogenetic Analysis and Comparative Data: A Test and Review of Evidence
inferredcites →https://doi.org/10.1093/aob/mci011openalex-snapshot
The Large Genome Constraint Hypothesis: Evolution, Ecology and Phenotype
inferredcites →https://doi.org/10.1093/aob/mci014openalex-snapshot
Evolution of DNA Amounts Across Land Plants (Embryophyta)
inferredcites →https://doi.org/10.1093/aob/mci019openalex-snapshot
The Origin, Evolution and Proposed Stabilization of the Terms 'Genome Size' and 'C-Value' to Describe Nuclear DNA Contents
inferredcites →https://doi.org/10.1093/aob/mcm321openalex-snapshot
Genome Size Scaling through Phenotype Space
inferredcites →https://doi.org/10.1093/aob/mcn230openalex-snapshot
Chromosome diversity and evolution in Liliaceae
inferredcites →https://doi.org/10.1093/aob/mcq011openalex-snapshot
Stomatal vs. genome size in angiosperms: the somatic tail wagging the genomic dog?
inferredcites →https://doi.org/10.1093/aob/mcr267openalex-snapshot
Genome size and DNA base composition of geophytes: the mirror of phenology and ecology?
inferredcites →https://doi.org/10.1093/aob/mcs222openalex-snapshot
New reports of nuclear DNA content for 407 vascular plant taxa from the United States
inferredcites →https://doi.org/10.1093/bioinformatics/btg412openalex-snapshot
APE: Analyses of Phylogenetics and Evolution in R language
inferredcites →https://doi.org/10.1093/bioinformatics/btm388openalex-snapshot
AWTY (are we there yet?): a system for graphical exploration of MCMC convergence in Bayesian phylogenetics
inferredcites →https://doi.org/10.1093/bioinformatics/btm404openalex-snapshot
Clustal W and Clustal X version 2.0
inferredcites →https://doi.org/10.1093/emboj/19.20.5562openalex-snapshot
Species‐specific double‐strand break repair and genome evolution in plants
inferredcites →https://doi.org/10.1093/sysbio/sys001openalex-snapshot
Overcoming Deep Roots, Fast Rates, and Short Internodes to Resolve the Ancient Rapid Radiation of Eupolypod II Ferns
inferredcites →https://doi.org/10.1093/sysbio/sys029openalex-snapshot
MrBayes 3.2: Efficient Bayesian Phylogenetic Inference and Model Choice Across a Large Model Space
inferredcites →https://doi.org/10.1098/rspb.1971.0066openalex-snapshot
The duration of meiosis
inferredcites →https://doi.org/10.1098/rspb.1972.0042openalex-snapshot
Nuclear DNA content and minimum generation time in herbaceous plants
inferredcites →https://doi.org/10.1105/tpc.9.9.1509openalex-snapshot
Do Plants Have a One-Way Ticket to Genomic Obesity?
inferredcites →https://doi.org/10.1111/j.0014-3820.2001.tb00731.xopenalex-snapshot
COMPARATIVE METHODS FOR THE ANALYSIS OF CONTINUOUS VARIABLES: GEOMETRIC INTERPRETATIONS
inferredcites →https://doi.org/10.1111/j.1095-8312.2004.00349.xopenalex-snapshot
Genome downsizing in polyploid plants
inferredcites →https://doi.org/10.1111/j.1399-3054.1977.tb04068.xopenalex-snapshot
The Importance of Cell Size in the Water Relations of Plants
inferredcites →https://doi.org/10.1111/j.1438-8677.2009.00268.xopenalex-snapshot
Genome size dynamics in Artemisia L. (Asteraceae): following the track of polyploidy
inferredcites →https://doi.org/10.1111/j.1469-185x.2000.tb00059.xopenalex-snapshot
Coincidence, coevolution, or causation? DNA content, cellsize, and the C‐value enigma
inferredcites →https://doi.org/10.1111/j.1469-8137.1987.tb04689.xopenalex-snapshot
VARIATION IN GENOMIC FORM IN PLANTS AND ITS ECOLOGICAL IMPLICATIONS
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01919.xopenalex-snapshot
Correlated evolution of genome size and seed mass
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.1469-8137.2012.04105.xopenalex-snapshot
Ecological and genetic factors linked to contrasting genome dynamics in seed plants
inferredcites →https://doi.org/10.1111/j.1558-5646.1954.tb00117.xopenalex-snapshot
RETICULATE EVOLUTION IN THE APPALACHIAN ASPLENIUMS
inferredcites →https://doi.org/10.1111/j.1558-5646.2009.00804.xopenalex-snapshot
SIZE-CORRECTION AND PRINCIPAL COMPONENTS FOR INTERSPECIFIC COMPARATIVE STUDIES
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/nph.12799openalex-snapshot
The contrasting effects of genome size, chromosome number and ploidy level on plant invasiveness: a global analysis
inferredcites →https://doi.org/10.1111/nph.13833openalex-snapshot
Genome evolution of ferns: evidence for relative stasis of genome size across the fern phylogeny
inferredcites →https://doi.org/10.1126/science.153.3733.305openalex-snapshot
Evolutionary Significance of Polyploidy in the Pteridophyta
inferredcites →https://doi.org/10.1126/science.264.5157.421openalex-snapshot
Stomatal Size in Fossil Plants: Evidence for Polyploidy in Majority of Angiosperms
inferredcites →https://doi.org/10.1139/b64-130openalex-snapshot
CHROMOSOME NUMBERS OF FERNS IN ONTARIO
inferredcites →https://doi.org/10.1139/b66-010openalex-snapshot
THE CYTOLOGY AND DISTRIBUTION OF DRYOPTERIS SPECIES IN ONTARIO
inferredcites →https://doi.org/10.1139/b79-225openalex-snapshot
Chromosome numbers in Canadian Phegopteris
inferredcites →https://doi.org/10.1139/gen-2015-0132openalex-snapshot
Genome size variation in the genus Avena
inferredcites →https://doi.org/10.1146/annurev.ge.05.120171.001321openalex-snapshot
THE GENETIC ORGANIZATION OF CHROMOSOMES
inferredcites →https://doi.org/10.1146/annurev.genet.34.1.401openalex-snapshot
POLYPLOID INCIDENCE AND EVOLUTION
inferredcites →https://doi.org/10.1146/annurev.pp.08.060157.001353openalex-snapshot
Drought Resistance in Plants and Physiological Processes
inferredcites →https://doi.org/10.1155/2010/316356openalex-snapshot
Endopolyploidy in Bryophytes: Widespread in Mosses and Absent in Liverworts
inferredcites →https://doi.org/10.1155/2010/612017openalex-snapshot
On the Relationship between Pollen Size and Genome Size
inferredcites →https://doi.org/10.11646/phytotaxa.19.1.2openalex-snapshot
A linear sequence of extant families and genera of lycophytes and ferns
inferredcites →https://doi.org/10.1186/1471-2105-11-7openalex-snapshot
TreeGraph 2: Combining and visualizing evidence from different phylogenetic analyses
inferredcites →https://doi.org/10.1186/1471-2229-13-219openalex-snapshot
Genome size expansion and the relationship between nuclear DNA content and spore size in the Asplenium monanthes fern complex (Aspleniaceae)
inferredcites →https://doi.org/10.1242/jcs.34.1.247openalex-snapshot
Nuclear volume control by nucleoskeletal DNA, selection for cell volume and cell growth rate, and the solution of the DNA C-value paradox
inferredcites →https://doi.org/10.1371/journal.pone.0026597openalex-snapshot
rbcL and matK Earn Two Thumbs Up as the Core DNA Barcode for Ferns
inferredcites →https://doi.org/10.14601/phytopathol_mediterr-14998u1.29openalex-snapshot
BIOEDIT: A USER-FRIENDLY BIOLOGICAL SEQUENCE ALIGNMENT EDITOR AND ANALYSIS PROGRAM FOR WINDOWS 95/98/ NT
inferredcites →https://doi.org/10.1525/bio.2010.60.3.4openalex-snapshot
Unfurling Fern Biology in the Genomics Age
inferredcites →https://doi.org/10.1590/2175-7860201566416openalex-snapshot
Flora of North America North of Mexico
inferredcites →https://doi.org/10.1640/0002-8444-99.2.117openalex-snapshot
2008 AFS Symposium Summary
inferredcites →https://doi.org/10.18637/jss.v022.i04openalex-snapshot
The ade4 Package: Implementing the Duality Diagram for Ecologists
inferredcites →https://doi.org/10.2307/1219449openalex-snapshot
PRINCIPAL COMPONENT ANALYSIS OF TAXONOMIC DATA WITH MULTI‐STATE DISCRETE CHARACTERS
inferredcites →https://doi.org/10.2307/1223038openalex-snapshot
Ferns and Fern Allies of Canada
inferredcites →https://doi.org/10.2307/1546181openalex-snapshot
Thelypteris in Northeastern North America
inferredcites →https://doi.org/10.2307/1546239openalex-snapshot
Pteridophytes of the Mountain Lake Area, Giles Co., Virginia: Biosystematic Studies, 1964-65
inferredcites →https://doi.org/10.2307/1547723openalex-snapshot
Systematic Inferences from Spore and Stomate Size in the Ferns
inferredcites →https://doi.org/10.2307/2395059openalex-snapshot
The Significance of Chromosome Numbers in Ferns
inferredcites →https://doi.org/10.2307/2399283openalex-snapshot
DNA Content Variation among Higher Plants
inferredcites →https://doi.org/10.2307/2419103openalex-snapshot
A Biosystematic Investigation of the Adiantum pedatum Complex in Eastern North America
inferredcites →https://doi.org/10.2307/25065646openalex-snapshot
A classification for extant ferns
inferredcites →https://doi.org/10.2307/25065903openalex-snapshot
Fern phylogeny inferred from 400 leptosporangiate species and three plastid genes
inferredcites →https://doi.org/10.2307/2805148openalex-snapshot
The Biota of Long-Distance Dispersal. III. Loss of Dispersibility in the Hawaiian Flora
inferredcites →https://doi.org/10.2307/2989770openalex-snapshot
Spore Germination and Viability in Pteridophyta: Evolutionary Significance of Chlorophyllous Spores
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.3732/ajb.0800079openalex-snapshot
Polyploidy and angiosperm diversification
inferredcites →https://doi.org/10.3732/ajb.0900206openalex-snapshot
Species boundaries and frequency of hybridization in the Dryopteris carthusiana (Dryopteridaceae) complex: A taxonomic puzzle resolved using genome size data
inferredcites →https://doi.org/10.3897/bdj.3.e6313openalex-snapshot
Biodiversity inventories in high gear: DNA barcoding facilitates a rapid biotic survey of a temperate nature reserve
inferredcites →https://doi.org/10.5962/bhl.title.4667openalex-snapshot
Problems of cytology and evolution in the Pteridophyta
inferredcites →https://doi.org/10.5962/bhl.title.53784openalex-snapshot
Ferns and fern allies of Canada

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.736.3.4zenodo-depositor-declared
Polystichum caucasicum sp. nov. (Dryopteridaceae), a new, surprisingly hexaploid fern species from the Caucasus
inferred← citeshttps://doi.org/10.1002/ajb2.16332openalex-snapshot
An adventurous journey toward and away from fern apomixis: Insights from genome size and spore abortion patterns
inferred← citeshttps://doi.org/10.1002/aps3.11452openalex-snapshot
A dormant resource for genome size estimation in ferns: C‐value inference of the Ophioglossaceae using herbarium specimen spores
inferred← citeshttps://doi.org/10.1002/tax.12180openalex-snapshot
A global plastid phylogeny of the cliff fern family Woodsiaceae and a two‐genus classification of Woodsiaceae with the description of ×Woodsimatium nothogen. nov.
inferred← citeshttps://doi.org/10.1007/978-981-16-6170-9_2openalex-snapshot
Genome Evolution in Ferns: Molecular Phylogenomics – A Review
inferred← citeshttps://doi.org/10.1007/s00497-023-00476-5openalex-snapshot
Interploidy gene flow via a ‘pentaploid bridge’ and ploidy reduction in Cystopteris fragilis fern complex (Cystopteridaceae: Polypodiales)
inferred← citeshttps://doi.org/10.1007/s00606-016-1285-7openalex-snapshot
Ploidy level and genome size variation in the homosporous ferns Botrychium s.l. (Ophioglossaceae)
inferred← citeshttps://doi.org/10.1016/j.foreco.2024.121767openalex-snapshot
Polyploidy – A tool in adapting trees to future climate changes? A review of polyploidy in trees
inferred← citeshttps://doi.org/10.1016/j.pld.2021.11.007openalex-snapshot
Genome size evolution of the extant lycophytes and ferns
inferred← citeshttps://doi.org/10.1016/j.ppees.2016.09.004openalex-snapshot
How genome size variation is linked with evolution within Chenopodium sensu lato
inferred← citeshttps://doi.org/10.1016/j.ympev.2019.05.004openalex-snapshot
Historical biogeography of the fern genus Polystichum (Dryopteridaceae) in Austral South America
inferred← citeshttps://doi.org/10.1017/pab.2025.8openalex-snapshot
Which morphological traits can be used to reconstruct genome size in fossil plants? Assessing sporomorph size and stomatal guard cell length as paleo-genome size proxies
inferred← citeshttps://doi.org/10.1093/aob/mcaf012openalex-snapshot
Distinct patterns of genome size evolution in each bryophyte lineage are not correlated with whole genome duplication
inferred← citeshttps://doi.org/10.1093/botlinnean/boaf054openalex-snapshot
Using stomatal length to indicate ploidy in the Dryopteris affinis (Dryopteridaceae) complex: does sampling location on the frond matter?
inferred← citeshttps://doi.org/10.1098/rspb.2020.1441openalex-snapshot
Genome size evolution: towards new model systems for old questions
inferred← citeshttps://doi.org/10.1111/jse.12226openalex-snapshot
Genetic and genomic aspects of hybridization in ferns
inferred← citeshttps://doi.org/10.1111/jse.12464openalex-snapshot
Polyphyletic Alyssum cuneifolium (Brassicaceae) revisited: Morphological and genome size differentiation of recently recognized allopatric taxa
inferred← citeshttps://doi.org/10.1111/jse.12525openalex-snapshot
Polyploidy does not control all: Lineage‐specific average chromosome length constrains genome size evolution in ferns
inferred← citeshttps://doi.org/10.1111/nph.13833openalex-snapshot
Genome evolution of ferns: evidence for relative stasis of genome size across the fern phylogeny
inferred← citeshttps://doi.org/10.1111/nph.71458openalex-snapshot
Divergent trajectories of genome architecture and chromosome evolution in ferns and angiosperms
inferred← citeshttps://doi.org/10.1127/nova_hedwigia/1235openalex-snapshot
A prophecy came true: Polypodium cambricum (Polypodiaceae) discovered in Germany, with a note on a new German occurrence of Polypodium × shivasiae
inferred← citeshttps://doi.org/10.1139/gen-2015-0132openalex-snapshot
Genome size variation in the genus Avena
inferred← citeshttps://doi.org/10.12705/651.2openalex-snapshot
Desmophlebiaceae and Desmophlebium : A new family and genus of Eupolypod II ferns
inferred← citeshttps://doi.org/10.1371/journal.pbio.2003706openalex-snapshot
Genome downsizing, physiological novelty, and the global dominance of flowering plants
inferred← citeshttps://doi.org/10.1590/0001-3765202120201881openalex-snapshot
State of the art in cytogenetics, insights into chromosome number evolution, and new C-value reports for the fern family Gleicheniaceae
inferred← citeshttps://doi.org/10.1640/0002-8444-107.2.59openalex-snapshot
Experimental Measurements of Terminal Velocity of Fern Spores
inferred← citeshttps://doi.org/10.1640/0002-8444-109.3.212openalex-snapshot
A Roadmap for Fern Genome Sequencing
inferred← citeshttps://doi.org/10.21203/rs.3.rs-10046045/v1openalex-snapshot
Contrasting genome-size constraints relate to divergent elemental strategies in bryophytes and tracheophytes
inferred← citeshttps://doi.org/10.21829/abm131.2024.2401openalex-snapshot
Desarrollo de la fase gametofítica de ocho especies de Pellaea (Pteridaceae, Polypodiophyta) presentes en México
inferred← citeshttps://doi.org/10.3389/fpls.2023.1183653openalex-snapshot
Phylogenomic analysis, cryptic species discovery, and DNA barcoding of the genus Cibotium in China based on plastome data
inferred← citeshttps://doi.org/10.3390/biology10040270openalex-snapshot
Genome Size Covaries More Positively with Propagule Size than Adult Size: New Insights into an Old Problem
inferred← citeshttps://doi.org/10.3897/bdj.3.e6313openalex-snapshot
Biodiversity inventories in high gear: DNA barcoding facilitates a rapid biotic survey of a temperate nature reserve
inferred← citeshttps://doi.org/10.3989/collectbot.2019.v38.010openalex-snapshot
Pellaea calomelanos (Pteridaceae) en Cataluña: es realmente una disyunción ancestral?
inferred← citeshttps://doi.org/10.5586/asbp.3564openalex-snapshot
It is worth checking old data – validation of Asplenium onopteris L. presence in the most northeastern sites in Europe (Sudetes, SW Poland)
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