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Reconstruction of ancestral genome size in Pitcairnioideae (Bromeliaceae): what can genome size tell us about the evolutionary history of its five genera?
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/anbo.1998.0730openalex-snapshot
Plant Genome Size Estimation by Flow Cytometry: Inter-laboratory Comparison*1
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/s00606-005-0306-8openalex-snapshot
Chromosomal features and evolution of Bromeliaceae
inferredcites →https://doi.org/10.1007/s00606-010-0370-6openalex-snapshot
Chromosome numbers and DNA C values in the genus Lippia (Verbenaceae)
inferredcites →https://doi.org/10.1007/s00606-012-0620-xopenalex-snapshot
Genome size and base composition of Bromeliaceae species assessed by flow cytometry
inferredcites →https://doi.org/10.1007/s00606-013-0784-zopenalex-snapshot
The first karyogram of a Bromeliaceae species: an allopolyploid genome
inferredcites →https://doi.org/10.1007/s00606-014-0985-0openalex-snapshot
Phylogeny and evolution of Dyckia (Bromeliaceae) inferred from chloroplast and nuclear sequences
inferredcites →https://doi.org/10.1007/s11240-011-0073-xopenalex-snapshot
Somatic embryogenesis from ovaries of sweet orange cv. Tobias
inferredcites →https://doi.org/10.1007/s11692-010-9093-4openalex-snapshot
Genome Size and Species Diversification
inferredcites →https://doi.org/10.1016/0092-8674(82)90148-9openalex-snapshot
On the formation of spontaneous deletions: The importance of short sequence homologies in the generation of large deletions
inferredcites →https://doi.org/10.1016/j.flora.2013.08.003openalex-snapshot
Invasion of the South American dry diagonal: What can the leaf anatomy of Pitcairnioideae (Bromeliaceae) tell us about it?
inferredcites →https://doi.org/10.1016/j.ympev.2009.01.001openalex-snapshot
Phylogenetic analysis of Fosterella L.B. Sm. (Pitcairnioideae, Bromeliaceae) based on four chloroplast DNA regions
inferredcites →https://doi.org/10.1016/s0169-5347(03)00184-8openalex-snapshot
Delimiting species: a Renaissance issue in systematic biology
inferredcites →https://doi.org/10.1021/bi00487a001openalex-snapshot
Misalignment-mediated DNA synthesis errors
inferredcites →https://doi.org/10.1038/nprot.2007.310openalex-snapshot
Estimation of nuclear DNA content in plants using flow cytometry
inferredcites →https://doi.org/10.1043/0363-6445-26.4.722openalex-snapshot
The Origin of the Low Chromosome Number in Cryptanthus (Bromeliaceae)
inferredcites →https://doi.org/10.1055/s-2004-817802openalex-snapshot
A Survey of Genetic Diversity and Reproductive Biology of Puya raimondii (Bromeliaceae), the Endangered Queen of the Andes
inferredcites →https://doi.org/10.1071/9780643090149openalex-snapshot
Monocots: Systematics and Evolution
inferredcites →https://doi.org/10.1073/pnas.1112041109openalex-snapshot
Extensive chromosomal variation in a recently formed natural allopolyploid species, Tragopogon miscellus (Asteraceae)
inferredcites →https://doi.org/10.1080/10635150490522232openalex-snapshot
Bayesian Estimation of Ancestral Character States on Phylogenies
inferredcites →https://doi.org/10.1080/11263500902722964openalex-snapshot
Plant species delimitation: A comparison of morphological and molecular markers
inferredcites →https://doi.org/10.1086/421067openalex-snapshot
Ancient Vicariance or Recent Long‐Distance Dispersal? Inferences about Phylogeny and South American–African Disjunctions in Rapateaceae and Bromeliaceae Based onndhF Sequence Data
inferredcites →https://doi.org/10.1093/aob/mci005openalex-snapshot
Plant DNA Flow Cytometry and Estimation of Nuclear Genome Size
inferredcites →https://doi.org/10.1093/aob/mci170openalex-snapshot
First Nuclear DNA Amounts in more than 300 Angiosperms
inferredcites →https://doi.org/10.1093/aob/mcq258openalex-snapshot
Nuclear DNA amounts in angiosperms: targets, trends and tomorrow
inferredcites →https://doi.org/10.1093/aob/mcr114openalex-snapshot
Chromosome pairing affinities in interspecific hybrids reflect phylogenetic distances among lady's slipper orchids (Paphiopedilum)
inferredcites →https://doi.org/10.1093/bioinformatics/btg180openalex-snapshot
MrBayes 3: Bayesian phylogenetic inference under mixed models
inferredcites →https://doi.org/10.1093/molbev/msr121openalex-snapshot
MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods
inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot
MUSCLE: multiple sequence alignment with high accuracy and high throughput
inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a010312openalex-snapshot
Plant Genome Size Estimation by Flow Cytometry: Inter-laboratory Comparison
inferredcites →https://doi.org/10.1093/sysbio/23.4.513openalex-snapshot
The Uniquely Evolved Character Concept and its Cladistic Application
inferredcites →https://doi.org/10.1098/rspb.2015.2289openalex-snapshot
Size is not everything: rates of genome size evolution, not C -value, correlate with speciation in angiosperms
inferredcites →https://doi.org/10.1098/rstb.1976.0044openalex-snapshot
Nuclear DNA amounts in angiosperms
inferredcites →https://doi.org/10.1101/gr.6096207openalex-snapshot
The mode and tempo of genome size evolution in eukaryotes
inferredcites →https://doi.org/10.1101/gr.8.3.175openalex-snapshot
Base-Calling of Automated Sequencer Traces Using Phred. I. Accuracy Assessment
inferredcites →https://doi.org/10.1111/boj.12211openalex-snapshot
Chromosome numbers and DNA content in Bromeliaceae: additional data and critical review
inferredcites →https://doi.org/10.1111/boj.12403openalex-snapshot
Phylogenetics of Pitcairnioideaes.s. (Bromeliaceae): evidence from nuclear and plastid DNA sequence data
inferredcites →https://doi.org/10.1111/j.1095-8312.2005.00503.xopenalex-snapshot
Towards integrative taxonomy
inferredcites →https://doi.org/10.1111/j.1095-8339.2008.00776.xopenalex-snapshot
Cytogenetics of Brazilian species of Bromeliaceae
inferredcites →https://doi.org/10.1111/j.1463-6409.1997.tb00423.xopenalex-snapshot
Inferring evolutionary processes from phylogenies
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03729.xopenalex-snapshot
Polyploid formation pathways have an impact on genetic rearrangements in resynthesized Brassica napus
inferredcites →https://doi.org/10.1111/jse.12044openalex-snapshot
A phylogeny of Bromeliaceae ( P oales, Monocotyledoneae) derived from an evaluation of nine supertree methods
inferredcites →https://doi.org/10.1146/annurev-ento-112408-085432openalex-snapshot
Integrative Taxonomy: A Multisource Approach to Exploring Biodiversity
inferredcites →https://doi.org/10.1146/annurev.arplant.043008.092039openalex-snapshot
The Role of Hybridization in Plant Speciation
inferredcites →https://doi.org/10.1146/annurev.ecolsys.35.112202.130128openalex-snapshot
Operational Criteria for Delimiting Species
inferredcites →https://doi.org/10.1159/000156416openalex-snapshot
Interactive Analysis of Phylogeny and Character Evolution Using the Computer Program MacClade
inferredcites →https://doi.org/10.1186/1471-2148-7-214openalex-snapshot
BEAST: Bayesian evolutionary analysis by sampling trees
inferredcites →https://doi.org/10.1186/1742-9994-7-16openalex-snapshot
The integrative future of taxonomy
inferredcites →https://doi.org/10.1186/s12862-014-0226-8openalex-snapshot
Inferring ancestral states without assuming neutrality or gradualism using a stable model of continuous character evolution
inferredcites →https://doi.org/10.1201/9780203165171.ch12openalex-snapshot
Ancestral states and evolutionary rates of continuous characters
inferredcites →https://doi.org/10.1371/journal.pbio.0040373openalex-snapshot
Detecting Non-Brownian Trait Evolution in Adaptive Radiations
inferredcites →https://doi.org/10.1371/journal.pone.0059784openalex-snapshot
Cytogenetic and Molecular Analyses Reveal a Divergence between Acromyrmex striatus (Roger, 1863) and Other Congeneric Species: Taxonomic Implications
inferredcites →https://doi.org/10.1590/0001-3765201420140224openalex-snapshot
Karyotype characterization and nuclear DNA content measurement in Bromeliaceae: State of the art and future perspectives
inferredcites →https://doi.org/10.1590/2175-7860201566411openalex-snapshot
Growing knowledge: an overview of Seed Plant diversity in Brazil
inferredcites →https://doi.org/10.1600/036364415x689186openalex-snapshot
Insights into the Evolution of Pitcairnia (Pitcairnioideae-Bromeliaceae), based on Morphological Evidence
inferredcites →https://doi.org/10.2307/2412809openalex-snapshot
The Evolutionary Species Concept Reconsidered
inferredcites →https://doi.org/10.2307/2419461openalex-snapshot
Phylogenetic Relationships in Subfamily Tillandsioideae (Bromeliaceae) Using ndhF Sequences
inferredcites →https://doi.org/10.2307/2807154openalex-snapshot
Disteganthus lateralis (Bromeliaceae), a New Combination for the Flora of Central French Guiana
inferredcites →https://doi.org/10.2307/2807789openalex-snapshot
Monocotyledons: Systematics and Evolution.
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.3732/ajb.1000059openalex-snapshot
Phylogeny, adaptive radiation, and historical biogeography in Bromeliaceae: Insights from an eight‐locus plastid phylogeny
inferredcites →https://doi.org/10.3732/ajb.1000415openalex-snapshot
Diversity and dynamics of plant genome size: An example of polysomaty from a cytogenetic study of Tahitian vanilla (Vanilla ×tahitensis, Orchidaceae)
inferredcites →https://doi.org/10.5281/zenodo.16031288openalex-snapshot
New combinations and new taxa in the Bromeliaceae
inferredcites →https://doi.org/10.5642/aliso.20072301.04openalex-snapshot
Phylogeny, Adaptive Radiation, and Historical Biogeography of Bromeliaceae Inferred from ndhF Sequence Data
inferredcites →https://doi.org/10.5642/aliso.20072301.05openalex-snapshot
Systematics of Bromelioideae (Bromeliaceae)—Evidence from Molecular and Anatomical Studies
inferredcites →https://doi.org/10.5860/choice.38-2161openalex-snapshot
Bromeliaceae: profile of an adaptive radiation
inferredcites →https://doi.org/10.5962/bhl.part.8052openalex-snapshot
New combinations in Mezobromelia and Racinaea (Bromeliaceae: Tillandsioideae)
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.595.2.4zenodo-depositor-declared
Dyckia magnifica, a new species of Bromeliaceae (Pitcairnioideae) from Southern Brazil, and the re-establishment of D. tomentosa, of the D. selloa complex
inferred← citeshttps://doi.org/10.11646/phytotaxa.729.1.1zenodo-depositor-declared
Taxonomic review of the Dyckia remotiflora complex (Bromeliaceae, Pitcairnioideae)
inferred← citeshttps://doi.org/10.1007/s00606-024-01933-yopenalex-snapshot
Genome size variation and whole-genome duplications in the monocot order Poales
inferred← citeshttps://doi.org/10.1038/s41598-019-41474-wopenalex-snapshot
Bromeliaceae subfamilies show divergent trends of genome size evolution
inferred← citeshttps://doi.org/10.1080/14772000.2019.1646834openalex-snapshot
Does nomenclatural stability justify para/polyphyletic taxa? A phylogenetic classification in the xeric clade Pitcairnioideae (Bromeliaceae)
inferred← citeshttps://doi.org/10.1093/botlinnean/boaa003openalex-snapshot
Bromeliaceae as a model group in understanding the evolution of Neotropical biota
inferred← citeshttps://doi.org/10.1093/botlinnean/boab095openalex-snapshot
Advances and perspectives on the evolutionary history and diversification of Neotropical Myrteae (Myrtaceae)
inferred← citeshttps://doi.org/10.1093/botlinnean/boz037openalex-snapshot
Interspecific gene flow and an intermediate molecular profile of Dyckia julianae (Bromeliaceae), an endemic species from southern Brazil
inferred← citeshttps://doi.org/10.1093/botlinnean/boz103openalex-snapshot
Genome size evolution and chromosome numbers of species of the cryptanthoid complex (Bromelioideae, Bromeliaceae) in a phylogenetic framework
inferred← citeshttps://doi.org/10.1093/zoolinnean/zlaa135openalex-snapshot
The tight genome size of ants: diversity and evolution under ancestral state reconstruction and base composition
inferred← citeshttps://doi.org/10.3389/fpls.2019.00205openalex-snapshot
What Do Nectarivorous Bats Like? Nectar Composition in Bromeliaceae With Special Emphasis on Bat-Pollinated Species
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