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Phylogenetics of Puya (Bromeliaceae): Placement, major lineages, and evolution of Chilean species

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What this work says

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

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CHROMOSOME NUMBERS IN BROMELIACEAE

inferredcites →https://doi.org/10.1002/j.1537-2197.1990.tb13616.xopenalex-snapshot

EVOLUTION OF POPULUS NIGRA (SECT. AIGEIROS):INTROGRESSIVE HYBRIDIZATION AND THE CHLOROPLAST CONTRIBUTION OF POPULUS ALBA (SECT. POPULUS)

inferredcites →https://doi.org/10.1006/clad.1996.0001openalex-snapshot

OPTIMIZATION ALIGNMENT: THE END OF MULTIPLE SEQUENCE ALIGNMENT IN PHYLOGENETICS?

inferredcites →https://doi.org/10.1006/clad.2001.0174openalex-snapshot

Majority Does Not Rule: The Trouble with Majority-Rule Consensus Trees

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Phylogeny of Poaceae Subfamily Pooideae Based on ChloroplastndhF Gene Sequences

inferredcites →https://doi.org/10.1007/978-1-4615-5419-6_10openalex-snapshot

Phylogenetic Incongruence: Window into Genome History and Molecular Evolution

inferredcites →https://doi.org/10.1007/bf00037152openalex-snapshot

Universal primers for amplification of three non-coding regions of chloroplast DNA

inferredcites →https://doi.org/10.1007/bf00161167openalex-snapshot

Relative rates of nucleotide substitution at the rbcl locus of monocotyledonous plants

inferredcites →https://doi.org/10.1007/bf00987959openalex-snapshot

Chloroplastrps16 intron phylogeny of the tribeSileneae (Caryophyllaceae)

inferredcites →https://doi.org/10.1007/bf01089742openalex-snapshot

Ecological patterns in theBromeliaceae of the lomas formations of Coastal Chile and Peru

inferredcites →https://doi.org/10.1007/bf02856593openalex-snapshot

Physiological ecology of the Bromeliaceae

inferredcites →https://doi.org/10.1007/s00606-005-0306-8openalex-snapshot

Chromosomal features and evolution of Bromeliaceae

inferredcites →https://doi.org/10.1007/s00606-006-0428-7openalex-snapshot

Ribosomal DNA evidence for the diversification of Tropaeolum sect. Chilensia (Tropaeolaceae)

inferredcites →https://doi.org/10.1016/j.ode.2003.12.001openalex-snapshot

A preliminary phylogeny of Loasaceae subfam. Loasoideae (Angiospermae: Cornales) based on L sequence data, with consequences for systematics and historical biogeography

inferredcites →https://doi.org/10.1016/j.ympev.2004.08.005openalex-snapshot

Phylogenetic analysis of the nuclear alcohol dehydrogenase (Adh) gene family in Carex section Acrocystis (Cyperaceae) and combined analyses of Adh and nuclear ribosomal ITS and ETS sequences for inferring species relationships

inferredcites →https://doi.org/10.1016/j.ympev.2006.05.003openalex-snapshot

Phylogeny of Chaetanthera (Asteraceae: Mutisieae) reveals both ancient and recent origins of the high elevation lineages

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/j.ympev.2009.02.003openalex-snapshot

Phylogeny of Bromelioideae (Bromeliaceae) inferred from nuclear and plastid DNA loci reveals the evolution of the tank habit within the subfamily

inferredcites →https://doi.org/10.1017/s0094837300002530openalex-snapshot

Pleistocene changes in the flora of the high tropical Andes

inferredcites →https://doi.org/10.1038/35002501openalex-snapshot

Biodiversity hotspots for conservation priorities

inferredcites →https://doi.org/10.1038/435041aopenalex-snapshot

Specialized bird perch aids cross-pollination

inferredcites →https://doi.org/10.1038/nature02243openalex-snapshot

Unmatched tempo of evolution in Southern African semi-desert ice plants

inferredcites →https://doi.org/10.1055/s-2000-3700openalex-snapshot

Molecular Phylogenetics of Bromeliaceae: Evidence from trnL(UAA) Intron Sequences of the Chloroplast Genome

inferredcites →https://doi.org/10.1071/bt97049openalex-snapshot

Track Analysis Reveals the Composite Nature of the Andean Biota

inferredcites →https://doi.org/10.1073/pnas.0400366101openalex-snapshot

Multiple origins of crassulacean acid metabolism and the epiphytic habit in the Neotropical family Bromeliaceae

inferredcites →https://doi.org/10.1073/pnas.0601928103openalex-snapshot

Island radiation on a continental scale: Exceptional rates of plant diversification after uplift of the Andes

inferredcites →https://doi.org/10.1080/10635150116801openalex-snapshot

Failure of the ILD to Determine Data Combinability for Slow Loris Phylogeny

inferredcites →https://doi.org/10.1080/10635150490264752openalex-snapshot

Congruence Versus Phylogenetic Accuracy: Revisiting the Incongruence Length Difference Test

inferredcites →https://doi.org/10.1080/10635150802429642openalex-snapshot

A Rapid Bootstrap Algorithm for the RAxML Web Servers

inferredcites →https://doi.org/10.1080/106351598260879openalex-snapshot

Biogeography and Floral Evolution of Baobabs Adansonia, Bombacaceae as Inferred From Multiple Data Sets

inferredcites →https://doi.org/10.1093/bioinformatics/14.9.817openalex-snapshot

MODELTEST: testing the model of DNA substitution.

inferredcites →https://doi.org/10.1093/bioinformatics/btg180openalex-snapshot

MrBayes 3: Bayesian phylogenetic inference under mixed models

inferredcites →https://doi.org/10.1093/bioinformatics/btl446openalex-snapshot

RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models

inferredcites →https://doi.org/10.1093/molbev/msl170openalex-snapshot

Bayesian Estimation of Concordance among Gene Trees

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025811openalex-snapshot

Bayesian phylogenetic inference using DNA sequences: a Markov Chain Monte Carlo Method

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026007openalex-snapshot

Usefulness of RNA polymerase II coding sequences for estimation of green plant phylogeny

inferredcites →https://doi.org/10.1093/sysbio/22.3.240openalex-snapshot

Maximum Likelihood and Minimum-Steps Methods for Estimating Evolutionary Trees from Data on Discrete Characters

inferredcites →https://doi.org/10.1111/j.0014-3820.2001.tb01312.xopenalex-snapshot

MOLECULAR PHYLOGEOGRAPHY, RETICULATION, AND LINEAGE SORTING IN MEDITERRANEAN SENECIO SECT. SENECIO (ASTERACEAE)

inferredcites →https://doi.org/10.1111/j.0908-8857.2004.03297.xopenalex-snapshot

Glacial history and colonization of Europe by the blue tit Parus caeruleus

inferredcites →https://doi.org/10.1111/j.1095-8312.2004.00368.xopenalex-snapshot

Molecular and morphological data reveal cryptic taxonomic diversity in the terrestrial slug complex Arion subfuscus/fuscus (Mollusca, Pulmonata, Arionidae) in continental north-west Europe

inferredcites →https://doi.org/10.1111/j.1095-8339.2007.00740.xopenalex-snapshot

Morphological phylogenetics of Puya subgenus Puya (Bromeliaceae)

inferredcites →https://doi.org/10.1111/j.1095-8339.2008.00926.xopenalex-snapshot

Systematic placement and biogeographical relationships of the monotypic generaGypothamniumandOxyphyllum(Asteraceae: Mutisioideae) from the Atacama Desert

inferredcites →https://doi.org/10.1111/j.1096-0031.1989.tb00573.xopenalex-snapshot

THE RETENTION INDEX AND THE RESCALED CONSISTENCY INDEX

inferredcites →https://doi.org/10.1111/j.1096-0031.1991.tb00036.xopenalex-snapshot

POLYMORPHIC TAXA, MISSING VALUES AND CLADISTIC ANALYSIS

inferredcites →https://doi.org/10.1111/j.1096-0031.1994.tb00179.xopenalex-snapshot

BRANCH SUPPORT AND TREE STABILITY

inferredcites →https://doi.org/10.1111/j.1096-0031.1994.tb00181.xopenalex-snapshot

TESTING SIGNIFICANCE OF INCONGRUENCE

inferredcites →https://doi.org/10.1111/j.1365-2699.2005.01349.xopenalex-snapshot

Inter‐ and intraspecific phylogeography of small mammals in the Atacama Desert and adjacent areas of northern Chile

inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb00420.xopenalex-snapshot

CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP

inferredcites →https://doi.org/10.1126/science.1061421openalex-snapshot

Rapid Diversification of a Species-Rich Genus of Neotropical Rain Forest Trees

inferredcites →https://doi.org/10.1126/science.1163197openalex-snapshot

Rates of Molecular Evolution Are Linked to Life History in Flowering Plants

inferredcites →https://doi.org/10.1126/science.173.3999.771openalex-snapshot

Pleistocene Changes in the Fauna and Flora of South America

inferredcites →https://doi.org/10.1146/annurev.ge.22.120188.002513openalex-snapshot

PHYLOGENIES FROM MOLECULAR SEQUENCES: INFERENCE AND RELIABILITY

inferredcites →https://doi.org/10.1600/036364408783887302openalex-snapshot

Molecular phylogeny of Persicaria (Persicarieae, Polygonaceae)

inferredcites →https://doi.org/10.1600/036364408785679815openalex-snapshot

Hybrid Origin and Genomic Mosaicism of Dubautia scabra (Hawaiian Silversword Alliance; Asteraceae, Madiinae)

inferredcites →https://doi.org/10.1663/0006-8101(2002)068[0153:pmaboc]2.0.co;2openalex-snapshot

Phylogeny, Morphology, and Biogeography of Chuquiraga, an Andean-Patagonian Genus of Asteraceae-Barnadesioideae

inferredcites →https://doi.org/10.2307/2399466openalex-snapshot

Effects of Aridity on Plant Diversity in the Northern Chilean Andes: Results of a Natural Experiment

inferredcites →https://doi.org/10.2307/2412304openalex-snapshot

Maximum Likelihood and Minimum-Steps Methods for Estimating Evolutionary Trees from Data on Discrete Characters

inferredcites →https://doi.org/10.2307/2419108openalex-snapshot

Taxonomic Realignments within the Subfamily Pitcairnioideae (Bromeliaceae)

inferredcites →https://doi.org/10.2307/2419763openalex-snapshot

A Phylogenetic Analysis of Epilobium (Onagraceae) Based on Nuclear Ribosomal DNA Sequences

inferredcites →https://doi.org/10.2307/2444413openalex-snapshot

Chromosome Numbers in Bromeliaceae

inferredcites →https://doi.org/10.2307/2445903openalex-snapshot

Examination of subfamilial phylogeny in Bromeliaceae using comparative sequencing of the plastid locus ndhF

inferredcites →https://doi.org/10.2307/2666671openalex-snapshot

Cladistic and Biogeographic Analyses of the Genera Moscharia and Polyachyrus (Asteraceae, Mutisieae)

inferredcites →https://doi.org/10.2307/3558360openalex-snapshot

Phylogeny of Malpighiaceae: evidence from chloroplast ndhF and trnl‐F nucleotide sequences

inferredcites →https://doi.org/10.3732/ajb.0800017openalex-snapshot

Phylogeny, biogeography, and rates of diversification of New World Astragalus (Leguminosae) with an emphasis on South American radiations

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.89.11.1826openalex-snapshot

Phylogeny of Capparaceae and Brassicaceae based on chloroplast sequence data

inferredcites →https://doi.org/10.3732/ajb.91.10.1700openalex-snapshot

Reconstructing patterns of reticulate evolution in plants

inferredcites →https://doi.org/10.3732/ajb.91.4.601openalex-snapshot

Phylogenetic relationships and biogeography of Fuchsia (Onagraceae) based on noncoding nuclear and chloroplast DNA data

inferredcites →https://doi.org/10.3732/ajb.92.1.132openalex-snapshot

Molecular phylogenetics of Phyllanthaceae: evidence from plastid MATK and nuclear PHYC sequences

inferredcites →https://doi.org/10.3732/ajb.92.1.142openalex-snapshot

The tortoise and the hare II: relative utility of 21 noncoding chloroplast DNA sequences for phylogenetic analysis

inferredcites →https://doi.org/10.3732/ajb.92.2.337openalex-snapshot

Phylogenetic relationships in subfamily Tillandsioideae (Bromeliaceae) based on DNA sequence data from seven plastid regions

inferredcites →https://doi.org/10.3732/ajb.94.3.275openalex-snapshot

Comparison of whole chloroplast genome sequences to choose noncoding regions for phylogenetic studies in angiosperms: the tortoise and the hare III

inferredcites →https://doi.org/10.3732/ajb.94.4.558openalex-snapshot

Phylogenetic relationships and ecological speciation in the mistletoe Tristerix (Loranthaceae): the influence of pollinators, dispersers, and hosts

inferredcites →https://doi.org/10.3732/ajb.95.2.229openalex-snapshot

Evolution of secondary heads in Nassauviinae (Asteraceae, Mutisieae)

inferredcites →https://doi.org/10.5169/seals-879232openalex-snapshot

Multi locus plastid phylogeny of Bromelioideae (Bromeliaceae) and the taxonomic utility of petal appendages and pollen characters

inferredcites →https://doi.org/10.5281/zenodo.16118190openalex-snapshot

Notes on Bromeliaceae, XXV

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/10.5962/bhl.part.21075openalex-snapshot

Notes on Bromeliaceae, XXVII

inferredcites →https://doi.org/10.5962/p.184538openalex-snapshot

Patterns of geographic distribution and their implications on the phylogeny of Puya (Bromeliaceae)

What points at this work

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

inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112581zenodo-depositor-declared

Identification of anthocyanin and other flavonoids from the green–blue petals of Puya alpestris (Bromeliaceae) and a clarification of their coloration mechanism

inferred← citeshttps://doi.org/10.11646/phytotaxa.261.1.2zenodo-depositor-declared

Morphological features, nuclear microsatellites and plastid haplotypes reveal hybridisation processes between two sympatric Vriesea species in Brazil (Bromeliaceae)

inferred← citeshttps://doi.org/10.1002/aps3.11308openalex-snapshot

Microsatellite markers for the endangered Puya raimondii in Peru

inferred← citeshttps://doi.org/10.1002/ece3.9159openalex-snapshot

Genetic markers in Andean Puya species (Bromeliaceae) with implications on plastome evolution and phylogeny

inferred← citeshttps://doi.org/10.1002/tax.595003openalex-snapshot

Ecology of plant speciation

inferred← citeshttps://doi.org/10.1002/tax.603004openalex-snapshot

Phylogenetic relationships and morphological diversity in Neotropical Heliotropium (Heliotropiaceae)

inferred← citeshttps://doi.org/10.1002/tax.604005openalex-snapshot

Revisiting monophyly in Haworthia Duval (Asphodelaceae): Incongruence, hybridization and contemporary speciation

inferred← citeshttps://doi.org/10.1007/978-3-662-56324-3_94-1openalex-snapshot

Puya BROMELIACEAE

inferred← citeshttps://doi.org/10.1007/978-3-662-56486-8_94openalex-snapshot

Puya BROMELIACEAE

inferred← citeshttps://doi.org/10.1007/978-90-481-8748-5_4openalex-snapshot

Biogeographic Regionalization

inferred← citeshttps://doi.org/10.1007/s00606-014-0985-0openalex-snapshot

Phylogeny and evolution of Dyckia (Bromeliaceae) inferred from chloroplast and nuclear sequences

inferred← citeshttps://doi.org/10.1007/s00606-015-1226-xopenalex-snapshot

Reproduction biology and chloroplast inheritance in Bromeliaceae: a case study in Fosterella (Pitcairnioideae)

inferred← citeshttps://doi.org/10.1007/s00606-017-1450-7openalex-snapshot

The evolutionary history of Senna ser. Aphyllae (Leguminosae–Caesalpinioideae), an endemic clade of southern South America

inferred← citeshttps://doi.org/10.1007/s10265-024-01531-6openalex-snapshot

Floral pigments and their perception by avian pollinators in three Chilean Puya species

inferred← citeshttps://doi.org/10.1007/s10682-014-9694-yopenalex-snapshot

Historical and ecological divergence among populations of Monttea chilensis (Plantaginaceae), an endemic endangered shrub bordering the Atacama Desert, Chile

inferred← citeshttps://doi.org/10.1007/s11240-016-0949-xopenalex-snapshot

Micropropagation of a giant ornamental bromeliad Puya berteroniana through adventitious shoots and assessment of their genetic stability through ISSR primers and flow cytometry

inferred← citeshttps://doi.org/10.1007/s12228-012-9290-9openalex-snapshot

Taxonomic revision of the Chilean Puya species (Puyoideae, Bromeliaceae), with special notes on the Puya alpestris-Puya berteroniana species complex

inferred← citeshttps://doi.org/10.1007/s12228-025-09858-7openalex-snapshot

A Fabulous Discovery: the second species of Puya (Bromeliaceae) in Brazil

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/10.1016/j.actao.2013.05.010openalex-snapshot

Morphology, nectar characteristics and avian pollinators in five Andean Puya species (Bromeliaceae)

inferred← citeshttps://doi.org/10.1016/j.avrs.2025.100267openalex-snapshot

The role of sterile apices of Puya chilensis (Bromeliaceae) on the nectar-feeding behavior of passeriform birds in central Chile

inferred← citeshttps://doi.org/10.1016/j.ygeno.2021.05.042openalex-snapshot

Draft genome of Puya raimondii (Bromeliaceae), the Queen of the Andes

inferred← citeshttps://doi.org/10.1016/j.ympev.2010.09.001openalex-snapshot

Detection of recent hybridization between sympatric Chilean Puya species (Bromeliaceae) using AFLP markers and reconstruction of complex relationships

inferred← citeshttps://doi.org/10.1016/j.ympev.2012.03.015openalex-snapshot

Molecular phylogenetics of the Brazilian giant bromeliads (Alcantarea, Bromeliaceae): implications for morphological evolution and biogeography

inferred← citeshttps://doi.org/10.1016/j.ympev.2013.10.010openalex-snapshot

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

inferred← citeshttps://doi.org/10.1016/j.ympev.2014.03.007openalex-snapshot

Molecular phylogeny of the Brazilian endemic genus Orthophytum (Bromelioideae, Bromeliaceae) and its implications on morphological character evolution

inferred← citeshttps://doi.org/10.1016/j.ympev.2015.09.028openalex-snapshot

Evolution of geographical place and niche space: Patterns of diversification in the North American sedge (Cyperaceae) flora

inferred← citeshttps://doi.org/10.1016/j.ympev.2016.03.001openalex-snapshot

Diversification of Bromelioideae (Bromeliaceae) in the Brazilian Atlantic rainforest: A case study in Aechmea subgenus Ortgiesia

inferred← citeshttps://doi.org/10.1016/j.ympev.2016.10.001openalex-snapshot

Resolving incongruence: Species of hybrid origin in Columnea (Gesneriaceae)

inferred← citeshttps://doi.org/10.1016/j.ympev.2016.10.019openalex-snapshot

Molecular phylogeny, character evolution and historical biogeography of Cryptanthus Otto & A. Dietr. (Bromeliaceae)

inferred← citeshttps://doi.org/10.1038/s41598-017-06638-6openalex-snapshot

Comparative Analysis of Four Buckwheat Species Based on Morphology and Complete Chloroplast Genome Sequences

inferred← citeshttps://doi.org/10.1071/fp10084openalex-snapshot

Evolution along the crassulacean acid metabolism continuum

inferred← citeshttps://doi.org/10.1071/fp17071openalex-snapshot

Concerted anatomical change associated with crassulacean acid metabolism in the Bromeliaceae

inferred← citeshttps://doi.org/10.1080/01916122.2026.2694051openalex-snapshot

Palynological study of species of Bromeliaceae belonging to subfamilies with restricted occurrence (Brocchinioideae, Hechtioideae, Lindmanioideae, Navioideae, and Puyoideae)

inferred← citeshttps://doi.org/10.1086/691214openalex-snapshot

Divergent Patterns of Selection on Crassulacean Acid Metabolism Photosynthesis in Contrasting Environments

inferred← citeshttps://doi.org/10.1093/aob/mcr291openalex-snapshot

Progenitor–derivative speciation in Pozoa (Apiaceae, Azorelloideae) of the southern Andes

inferred← citeshttps://doi.org/10.1093/aobpla/ply008openalex-snapshot

Geography, environment and organismal traits in the diversification of a major tropical herbaceous angiosperm radiation

inferred← citeshttps://doi.org/10.1093/botlinnean/boab045openalex-snapshot

Hybridization and species boundaries between three sympatric bromeliads from the Brazilian Atlantic Forest

inferred← citeshttps://doi.org/10.1093/botlinnean/boab102openalex-snapshot

Recent divergence in functional traits affects rates of speciation in the Neotropical Velloziaceae (Pandanales)

inferred← citeshttps://doi.org/10.1093/botlinnean/boac042openalex-snapshot

Biotic and abiotic factors in promoting the starting point of hybridization in the Neotropical flora: implications for conservation in a changing world

inferred← citeshttps://doi.org/10.1093/botlinnean/boae074openalex-snapshot

New insights into the classification, diversification, and evolutionary dynamics of bromeliads

inferred← citeshttps://doi.org/10.1093/botlinnean/boz038openalex-snapshot

Historical biogeography of a Brazilian lineage of Tillandsioideae (subtribe Vrieseinae, Bromeliaceae): the Paranaean Sea hypothesized as the main vicariant event

inferred← citeshttps://doi.org/10.1093/botlinnean/boz102openalex-snapshot

Systematics of Vriesea (Bromeliaceae): phylogenetic relationships based on nuclear gene and partial plastome sequences

inferred← citeshttps://doi.org/10.1093/botlinnean/boz108openalex-snapshot

Comparative phylogeography, morphological boundaries and climate envelopes of two sympatric widespread Bromeliaceae from the southern Andes

inferred← citeshttps://doi.org/10.1093/sysbio/syt052openalex-snapshot

Constructing Phylogenies in the Presence Of Intra-Individual Site Polymorphisms (2ISPs) with a Focus on the Nuclear Ribosomal Cistron

inferred← citeshttps://doi.org/10.1101/2022.02.18.480924openalex-snapshot

Description of Life History and Reproductive Size Thresholds in Three High Elevation Puya (Bromeliaceae)

inferred← citeshttps://doi.org/10.1101/857441openalex-snapshot

Serpentine mountain uplift in northern Japan triggered the divergence of a narrow endemic from a widespread (sub)arctic Asia-Alaska species complex of Lagotis (Plantaginaceae)

inferred← citeshttps://doi.org/10.1111/bij.12297openalex-snapshot

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

inferred← citeshttps://doi.org/10.1111/boj.12275openalex-snapshot

Photosynthetic pathways in Bromeliaceae: phylogenetic and ecological significance of CAM and C 3 based on carbon isotope ratios for 1893 species

inferred← citeshttps://doi.org/10.1111/boj.12400openalex-snapshot

Disentangling theTillandsia capillariscomplex: phylogenetic relationships and taxon boundaries in Andean populations

inferred← citeshttps://doi.org/10.1111/boj.12403openalex-snapshot

Phylogenetics of Pitcairnioideaes.s. (Bromeliaceae): evidence from nuclear and plastid DNA sequence data

inferred← citeshttps://doi.org/10.1111/boj.12425openalex-snapshot

Phylogenetics and evolution of theTillandsia utriculatacomplex (Bromeliaceae, Tillandsioideae) inferred from three plastid DNA markers and the ETS of the nuclear ribosomal DNA

inferred← citeshttps://doi.org/10.1111/boj.12431openalex-snapshot

Advances in and perspectives on evolution in Bromeliaceae

inferred← citeshttps://doi.org/10.1111/ddi.13004openalex-snapshot

Biogeography and conservation status of the pineapple family (Bromeliaceae)

inferred← citeshttps://doi.org/10.1111/j.1095-8312.2011.01713.xopenalex-snapshot

Crassulacean acid metabolism photosynthesis in Bromeliaceae: an evolutionary key innovation

inferred← citeshttps://doi.org/10.1111/j.1095-8339.2012.01295.xopenalex-snapshot

Phylogenetic relationships and distribution of New World Melastomeae (Melastomataceae)

inferred← citeshttps://doi.org/10.1111/j.1095-8339.2012.01307.xopenalex-snapshot

Historical biogeography and life-history evolution of Andean Puya (Bromeliaceae)

inferred← citeshttps://doi.org/10.1111/j.1095-8339.2012.01325.xopenalex-snapshot

The South American radiation ofLepechinia(Lamiaceae): phylogenetics, divergence times and evolution of dioecy

inferred← citeshttps://doi.org/10.1111/j.1365-2699.2011.02658.xopenalex-snapshot

Disrupted phylogeographical microsatellite and chloroplast DNA patterns indicate a vicariance rather than long‐distance dispersal origin for the disjunct distribution of the Chilean endemic Dioscorea biloba (Dioscoreaceae) around the Atacama Desert

inferred← citeshttps://doi.org/10.1111/jbi.13237openalex-snapshot

Crassulacean acid metabolism and distribution range in Chilean Bromeliaceae: Influences of climate and phylogeny

inferred← citeshttps://doi.org/10.1111/jse.12044openalex-snapshot

A phylogeny of Bromeliaceae ( P oales, Monocotyledoneae) derived from an evaluation of nine supertree methods

inferred← citeshttps://doi.org/10.1111/jse.13004openalex-snapshot

Expansions and contractions of the inverted repeat, as well as gene loss and potential pseudogenization shape plastome evolution in Hechtioideae (Bromeliaceae, Poales)

inferred← citeshttps://doi.org/10.1111/jse.13062openalex-snapshot

Phylogenomics of Puya (Bromeliaceae): Evolution in the Andean slopes and sky island ecosystems

inferred← citeshttps://doi.org/10.1111/njb.03239openalex-snapshot

A new rupicolous species of Puya (Bromeliaceae) with pendulous inflorescence from the Eastern Cordillera of Colombia

inferred← citeshttps://doi.org/10.1111/nph.20036openalex-snapshot

The ‘queen of the Andes’ (Puya raimondii) is genetically fragile and fragmented: a consequence of long generation time and semelparity?

inferred← citeshttps://doi.org/10.1146/annurev-ecolsys-121415-032330openalex-snapshot

Mediterranean Biomes: Evolution of Their Vegetation, Floras, and Climate

inferred← citeshttps://doi.org/10.1177/1934578x221091671openalex-snapshot

Cytotoxic Effect of Puya chilensis Collected in Central Chile

inferred← citeshttps://doi.org/10.1186/s12862-015-0388-zopenalex-snapshot

The temporal build-up of hummingbird/plant mutualisms in North America and temperate South America

inferred← citeshttps://doi.org/10.1371/journal.pone.0110029openalex-snapshot

Latitudinal Environmental Niches and Riverine Barriers Shaped the Phylogeography of the Central Chilean Endemic Dioscorea humilis (Dioscoreaceae)

inferred← citeshttps://doi.org/10.1371/journal.pone.0128559openalex-snapshot

Munroa argentina, a Grass of the South American Transition Zone, Survived the Andean Uplift, Aridification and Glaciations of the Quaternary

inferred← citeshttps://doi.org/10.15381/rpb.v28i2.18115openalex-snapshot

Nuevos registros de Puya (Bromeliaceae) en el departamento de Lambayeque, Perú

inferred← citeshttps://doi.org/10.15446/caldasia.v36n1.43891openalex-snapshot

PUYA HAMATA DEMOGRAPHY AS AN INDICATOR OF RECENT FIRE HISTORY IN THE PÁRAMO OF EL ÁNGEL AND VOLCÁN CHILES, ECUADOR-COLOMBIA

inferred← citeshttps://doi.org/10.1590/2175-7860201566218openalex-snapshot

Morphological Phylogenetic Analysis of Two Early-Diverging Genera of Bromelioideae (Bromeliaceae)

inferred← citeshttps://doi.org/10.1600/036364411x605047openalex-snapshot

Testing the Monophyly and Placement of Lepechinia in the Tribe Mentheae (Lamiaceae)

inferred← citeshttps://doi.org/10.1600/036364414x681554openalex-snapshot

Molecular Phylogeny Estimation of the Bamboo Genus Chusquea (Poaceae: Bambusoideae: Bambuseae) and Description of Two New Subgenera

inferred← citeshttps://doi.org/10.1600/036364415x686413openalex-snapshot

Phylogenetic Relationships in Bromeliaceae Subfamily Bromelioideae based on Chloroplast DNA Sequence Data

inferred← citeshttps://doi.org/10.1600/036364422x16512564801696openalex-snapshot

Molecular Phylogenetics and Trait Evolution in Stigmatodon (Bromeliaceae, Tillandsioideae), an Endemic Genus to Brazilian Rocky Outcrops

inferred← citeshttps://doi.org/10.17129/botsci.3389openalex-snapshot

Re-establishment of Aechmea laxiflora (Bromeliaceae, Bromelioideae) based on morphological and phylogenetic evidence, with notes on its geographical distribution

inferred← citeshttps://doi.org/10.18257/raccefyn.223openalex-snapshot

Una nueva especie de Puya (Bromeliaceae) de los páramos cercanos a Bogotá, Colombia

inferred← citeshttps://doi.org/10.2525/ecb.50.305openalex-snapshot

Morphological and Molecular Analyses of Rheophytic Rhododendron ripense and Its Allied Dryland Species R. macrosepalum (Ericaceae)

inferred← citeshttps://doi.org/10.2985/015.089.0406openalex-snapshot

A New Species of Puya (Bromeliaceae) from Coastal Peru

inferred← citeshttps://doi.org/10.3389/fevo.2021.668281openalex-snapshot

Genome Skimming Reveals Widespread Hybridization in a Neotropical Flowering Plant Radiation

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

inferred← citeshttps://doi.org/10.3389/fpls.2025.1549351openalex-snapshot

Phylogeny, structural patterns, and polymorphisms in Dyckia spp. from the Espinhaço mountain range based on complete chloroplast genome

inferred← citeshttps://doi.org/10.3390/plants12203654openalex-snapshot

Ecogeography of Dioscorea remotiflora Kunth: An Endemic Species from Mexico

inferred← citeshttps://doi.org/10.3390/plants13212989openalex-snapshot

Phytoconstituents, Antioxidant Activity and Cytotoxicity of Puya chilensis Mol. Extracts in Colon Cell Lines

inferred← citeshttps://doi.org/10.3732/ajb.1000059openalex-snapshot

Phylogeny, adaptive radiation, and historical biogeography in Bromeliaceae: Insights from an eight‐locus plastid phylogeny

inferred← citeshttps://doi.org/10.3732/ajb.1300048openalex-snapshot

Systematics, biogeography, and character evolution of Sparganium (Typhaceae): Diversification of a widespread, aquatic lineage

inferred← citeshttps://doi.org/10.3732/ajb.1600410openalex-snapshot

Population genetic structure of the rock outcrop species Encholirium spectabile (Bromeliaceae): The role of pollination vs. seed dispersal and evolutionary implications

inferred← citeshttps://doi.org/10.4067/s0718-34022011000300007openalex-snapshot

Hacia una fitogeografía histórica del Desierto de Atacama

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