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Systematics of Nothofagus (Nothofagaceae) based on rDNA spacer sequences (ITS): taxonomic congruence with morphology and plastid sequences
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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MONOPHYLY OF ANEUPLOID ASTRAGALUS (FABACEAE): EVIDENCE FROM NUCLEAR RIBOSOMAL DNA INTERNAL TRANSCRIBED SPACER SEQUENCES
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Cretaceous Paleobotany and Its Bearing on the Biogeography of Austral Angiosperms
inferredcites →https://doi.org/10.1007/bf00039493openalex-snapshot
A conserved core structure in the 18?25S rRNA intergenic region from tobacco, Nicotiana rustica
inferredcites →https://doi.org/10.1007/bf01481819openalex-snapshot
On the New Zealand wild hybrids of Nothofagus
inferredcites →https://doi.org/10.1016/0031-0182(80)90019-xopenalex-snapshot
New Zealand late Cretaceous and cenozoic plant biogeography: A contribution
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Phylogenetic utility of the internal transcribed spacers of nuclear ribosomal DNA in plants: An example from the compositae
inferredcites →https://doi.org/10.1029/jb087ib06p04697openalex-snapshot
Uncertainties in the relative positions of the Australia, Antarctica, Lord Howe, and Pacific Plates since the Late Cretaceous
inferredcites →https://doi.org/10.1071/bt9550197openalex-snapshot
The pollen morphology of Nothofagus BL. subsection Bipartitae Steen
inferredcites →https://doi.org/10.1071/sb9930111openalex-snapshot
The evolutionary history of Nothofagus (Nothofagaceae)
inferredcites →https://doi.org/10.1071/sb9930441openalex-snapshot
Using Sequences of rbc L to Study Phylogeny and Biogeography of Nothofagus Species
inferredcites →https://doi.org/10.1073/pnas.92.7.2647openalex-snapshot
Chloroplast gene sequence data suggest a single origin of the predisposition for symbiotic nitrogen fixation in angiosperms.
inferredcites →https://doi.org/10.1080/00167617808729012openalex-snapshot
The southwest pacific area during the last 90 million years
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Casuarinaceae, Fagaceae, and other plant megafossils from Kaikorai Leaf Beds (Miocene) Kaikorai Valley, Dunedin, New Zealand
inferredcites →https://doi.org/10.1080/03115518408619610openalex-snapshot
TertiaryNothofagusmacrofossils from Cethana, Tasmania
inferredcites →https://doi.org/10.1086/297231openalex-snapshot
Fagaceous Flowers, Fruits, and Cupules from the Campanian (Late Cretaceous) of Central Georgia, USA
inferredcites →https://doi.org/10.1093/sysbio/30.3.351openalex-snapshot
The Implications of Congruence in Menidia
inferredcites →https://doi.org/10.1093/sysbio/38.1.7openalex-snapshot
A Concern for Evidence and a Phylogenetic Hypothesis of Relationships among Epicrates (Boidae, Serpentes)
inferredcites →https://doi.org/10.1111/j.1095-8339.1988.tb01692.xopenalex-snapshot
A classification of the genus Nothofagus (Fagaceae)
inferredcites →https://doi.org/10.1111/j.1095-8339.1991.tb00199.xopenalex-snapshot
A revised infrageneric classification of Nothofagus (Fagaceae)
inferredcites →https://doi.org/10.1111/j.1095-8339.1996.tb00743.xopenalex-snapshot
Leaf architecture of South American Nothofagus (Nothofagaceae) using traditional and new methods in morphometrics
inferredcites →https://doi.org/10.1111/j.1096-0031.1995.tb00002.xopenalex-snapshot
NOTHOFAGUSAND PACIFIC BIOGEOGRAPHY
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Origins and Evolution of the Antarctic Biota
inferredcites →https://doi.org/10.1111/j.1558-5646.1965.tb03325.xopenalex-snapshot
ON THE REAL NATURE OF TRANSANTARCTIC RELATIONSHIPS,
inferredcites →https://doi.org/10.1126/science.95.2455.69openalex-snapshot
Continental Drift and Plant Distribution
inferredcites →https://doi.org/10.2307/2395196openalex-snapshot
Historical Biogeography and Earth History: Perspectives for a Future Synthesis
inferredcites →https://doi.org/10.2307/2399880openalex-snapshot
The its Region of Nuclear Ribosomal DNA: A Valuable Source of Evidence on Angiosperm Phylogeny
inferredcites →https://doi.org/10.2307/2419533openalex-snapshot
Cladistic Analysis of Restriction Site Variation within the Chloroplast DNA Inverted Repeat Region of Selected Hamamelididae
inferredcites →https://doi.org/10.2307/2446139openalex-snapshot
Phylogenetic analyses of “higher” Hamamelididae based on plastid sequence data
inferredcites →https://doi.org/10.2307/2997028openalex-snapshot
Leaf Morphology and a Key to Species of Nothofagus Bl.
inferredcites →https://doi.org/10.5962/bhl.part.27154openalex-snapshot
Results of the Archbold expeditions Papuan nothofagus
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Revised circumscription of Nothofagus and recognition of the segregate genera Fuscospora, Lophozonia, and Trisyngyne (Nothofagaceae)
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Population genetic structure, genetic diversity, and natural history of the South American species of Nothofagus subgenus Lophozonia (Nothofagaceae) inferred from nuclear microsatellite data
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Complex History of Organellar Introgression in Nothofagus Trees: Chloroplast and Mitochondrial Capture Facilitated by Natural Selection
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Nothofagus Biogeography Revisited with Special Emphasis on the Enigmatic Distribution of Subgenus Brassospora in New Caledonia
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Nothofagus, Key Genus in Plant Geography
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Molecular phylogeny ofNothofagus (Nothofagaceae) based on theatpB-rbcL intergenic spacer of the chloroplast DNA
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The classification and geography of the flowering plants: Dicotyledons of the class Angiospermae
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Comparison of ISSR and RAPD markers to characterize three Chilean Nothofagus species
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Chloroplast DNA markers reveal a geographical divide across Argentinean southern beech Nothofagus nervosa (Phil.) Dim. et Mil. distribution area
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Xylem anatomy and calculated hydraulic conductance of four Nothofagus species with contrasting distribution in South-Central Chile
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Species richness of herbivorous insects on Nothofagus trees in South America and New Zealand: The importance of chemical attributes of the host
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Natural products isolation studies of the paleoendemic plant species Nothofagus gunnii and Nothofagus cunninghamii
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The effect of silvicultural management on the genetic diversity of a mixed Nothofagus forest in Lanín Natural Reserve, Argentina
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Macroevolutionary changes in the fossil plant record: Key examples from the Cretaceous-Paleogene of Patagonia, Argentina
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Evolution of the New Zealand mountain flora: Origins, diversification and dispersal
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Taxonomic turnover and abundance in Cretaceous to Tertiary wood floras of Antarctica: implications for changes in forest ecology
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Characterizing regions of ambiguous alignment caused by the expansion and contraction of hairpin-stem loops in ribosomal RNA molecules
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Is there a molecular key to the level of “biological species” in eukaryotes? A DNA guide
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Evidence of chloroplast capture in South American Nothofagus (subgenus Nothofagus, Nothofagaceae)
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Halfway encounters: Meeting points of colonization routes among the southern beeches Nothofagus pumilio and N. antarctica
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The Vegetation of Antarctica through Geological Time
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Microsatellites for use in Nothofagus cunninghamii (Nothofagaceae) and related species
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Gondwana, vicariance biogeography and the New York School revisited
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Biogeography, evolution and palaeoecology of Nothofagus (Nothofagaceae): the contribution of the fossil record
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Most parsimonious areagrams versus fossils: the case of Nothofagus (Nothofagaceae)
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Bark anatomy of Nothofagus species (Nothofagaceae) indigenous to the Andean–Patagonian forest, Argentina
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Phytogeography and climate analysis of Nothofagus subgenus Brassospora in New Guinea and New Caledonia
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Instantaneous photosynthetic responses to temperature of deciduous and evergreen Nothofagus species
inferred← citeshttps://doi.org/10.1071/is07032openalex-snapshot
Relationships among felt scale insects (Hemiptera : Coccoidea : Eriococcidae) of southern beech, Nothofagus (Nothofagaceae), with the first descriptions of Australian species of the Nothofagus-feeding genus Madarococcus Hoy
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Track analysis of agaricoid fungi of the Patagonian forests
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inferred← citeshttps://doi.org/10.1073/pnas.0510383103openalex-snapshot
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inferred← citeshttps://doi.org/10.1079/cabicompendium.36433openalex-snapshot
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Characterisation of seven polymorphic microsatellites for Nothofagus subgenus Fuscospora from New Zealand
inferred← citeshttps://doi.org/10.1080/0028825x.2014.960946openalex-snapshot
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Characterisation and transferability of transcriptomic microsatellite markers for Nothofagus species
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Plio‐Pleistocene environmental changes shape present day phylogeography of New Zealand's southern beeches (Nothofagaceae)
inferred← citeshttps://doi.org/10.1080/00779962.2025.2491142openalex-snapshot
Biotectonic analysis of Tasmania-New Zealand connections with special reference to Coleoptera
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Variation in leaf morphology and chloroplast DNA in Ulmus glabra in the northern suture zone: Effects of distinct glacial refugia
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Paleocene flora from Seymour Island, Antarctica: revision of Dusén’s (1908) angiosperm taxa
inferred← citeshttps://doi.org/10.1080/08912963.2015.1136930openalex-snapshot
Paleofloristic assemblage from the Paleogene Río Guillermo Formation, Argentina: preliminary results of phylogenetic relationships ofNothofagusin South America
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Ancient Antarctica: the early evolutionary history ofNothofagus
inferred← citeshttps://doi.org/10.1080/106351500750049743openalex-snapshot
Integrating Ambiguously Aligned Regions of DNA Sequences in Phylogenetic Analyses Without Violating Positional Homology
inferred← citeshttps://doi.org/10.1080/10635150309331openalex-snapshot
18S Ribosomal RNA and Tetrapod Phylogeny
inferred← citeshttps://doi.org/10.1080/10635150490423430openalex-snapshot
Southern Hemisphere Biogeography Inferred by Event-Based Models: Plant versus Animal Patterns
inferred← citeshttps://doi.org/10.1080/10635150601156305openalex-snapshot
Opinions on Multiple Sequence Alignment, and an Empirical Comparison of Repeatability and Accuracy between POY and Structural Alignment
inferred← citeshttps://doi.org/10.1080/17429140701861735openalex-snapshot
Monoterpene emissions from threeNothofagusspecies in Patagonia, Argentina
inferred← citeshttps://doi.org/10.1086/297559openalex-snapshot
New Genus of Fossil Fagaceae from the Santonian (Late Cretaceous) of Central Georgia, U. S. A.
inferred← citeshttps://doi.org/10.1086/297584openalex-snapshot
Stamen Morphology in Nothofagus (Nothofagaceae)
inferred← citeshttps://doi.org/10.1086/314090openalex-snapshot
Ontogeny and Diversity in Staminate Flowers ofNothofagus(Nothofagaceae)
inferred← citeshttps://doi.org/10.1086/314207openalex-snapshot
The Phylogenetic Affinities of Nothofagus (Nothofagaceae) Leaf Fossils based on Combined Molecular and Morphological Data
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Clades, Clocks, and Continents: Historical and Biogeographical Analysis of Myrtaceae, Vochysiaceae, and Relatives in the Southern Hemisphere
inferred← citeshttps://doi.org/10.1086/424022openalex-snapshot
Tropical Intercontinental Disjunctions: Gondwana Breakup, Immigration from the Boreotropics, and Transoceanic Dispersal
inferred← citeshttps://doi.org/10.1093/aob/mcf012openalex-snapshot
Periods of Organogenesis in Shoots of Nothofagus dombeyi (Mirb.) Oersted (Nothofagaceae)
inferred← citeshttps://doi.org/10.1093/aob/mch205openalex-snapshot
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Genetic Diversity in Nothofagus alessandrii (Fagaceae), an Endangered Endemic Tree Species of the Coastal Maulino Forest of Central Chile
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/botlinnean/boaa097openalex-snapshot
The micro- and megafossil record of Nothofagaceae from South America
inferred← citeshttps://doi.org/10.1093/jhered/esae032openalex-snapshot
Plastomes of Nothofagus reflect a shared biogeographic history in Patagonia
inferred← citeshttps://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)
inferred← citeshttps://doi.org/10.1098/rspb.2001.1782openalex-snapshot
Evolution of the angiosperms: calibrating the family tree
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Not so ancient: the extant crown group of Nothofagus represents a post-Gondwanan radiation
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Radiation of the Australian flora: what can comparisons of molecular phylogenies across multiple taxa tell us about the evolution of diversity in present–day communities?
inferred← citeshttps://doi.org/10.1111/boj.12143openalex-snapshot
NothofagussubgenusBrassospora(Nothofagaceae) leaf fossils from New Zealand: a link to Australia and New Guinea?
inferred← citeshttps://doi.org/10.1111/curt.12599openalex-snapshot
1120. Nothofagus cunninghamii (Hook.) Oerst
inferred← citeshttps://doi.org/10.1111/curt.12603openalex-snapshot
The Southern Beeches: an introduction to the genus Nothofagus Blume
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The biogeography of the austral, subalpine genus Ourisia (Plantaginaceae) based on molecular phylogenetic evidence: South American origin and dispersal to New Zealand and Tasmania
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Evolution in Apiales: nuclear and chloroplast markers together in (almost) perfect harmony
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Time and tempo of diversification in the flora of New Caledonia
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Are Chilean coastal forests pre‐Pleistocene relicts? Evidence from foliar physiognomy, palaeoclimate, and phytogeography
inferred← citeshttps://doi.org/10.1111/j.1365-2699.2006.01479.xopenalex-snapshot
Panbiogeography of Nothofagus (Nothofagaceae): analysis of the main species massings
inferred← citeshttps://doi.org/10.1111/j.1365-2699.2006.01655.xopenalex-snapshot
West Wind Drift revisited: testing for directional dispersal in the Southern Hemisphere using event‐based tree fitting
inferred← citeshttps://doi.org/10.1111/j.1365-2699.2007.01802.xopenalex-snapshot
The barriers to oceanic island radiation in bryophytes: insights from the phylogeography of the moss Grimmia montana
inferred← citeshttps://doi.org/10.1111/j.1365-2699.2009.02221.xopenalex-snapshot
Use of dispersal–vicariance analysis in biogeography – a critique
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2009.04294.xopenalex-snapshot
New Zealand phylogeography: evolution on a small continent
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2009.04456.xopenalex-snapshot
Out in the cold: genetic variation of Nothofagus pumilio (Nothofagaceae) provides evidence for latitudinally distinct evolutionary histories in austral South America
inferred← citeshttps://doi.org/10.1111/j.1466-8238.2010.00595.xopenalex-snapshot
Historical and phylogenetic constraints on the incidence of entire leaf margins: insights from a new South American model
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2008.02761.xopenalex-snapshot
The major Australian cool temperate rainforest tree Nothofagus cunninghamii withstood Pleistocene glacial aridity within multiple regions: evidence from the chloroplast
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2011.03861.xopenalex-snapshot
Phylogeographically concordant chloroplast DNA divergence in sympatric Nothofagus s.s. How deep can it be?
inferred← citeshttps://doi.org/10.1111/j.1529-8817.2008.00556.xopenalex-snapshot
PHYLOGENETIC PATTERNS AMONG NOSTOC CYANOBIONTS WITHIN BI‐ AND TRIPARTITE LICHENS OF THE GENUS PANNARIA1
inferred← citeshttps://doi.org/10.1111/j.1574-6941.2011.01183.xopenalex-snapshot
Yeast communities associated with the bulk-soil, rhizosphere and ectomycorrhizosphere of a Nothofagus pumilio forest in northwestern Patagonia, Argentina
inferred← citeshttps://doi.org/10.1139/cjm-2013-0897openalex-snapshot
Ecology of cultivable yeasts in pristine forests in northern Patagonia (Argentina) influenced by different environmental factors
inferred← citeshttps://doi.org/10.1144/gsl.sp.2006.258.01.05openalex-snapshot
Cretaceous and Cenozoic vegetation of Antarctica integrating the fossil wood record
inferred← citeshttps://doi.org/10.11464/diatom1985.13.0_25openalex-snapshot
Genera, species and varieties - are problems real or imagined?
inferred← citeshttps://doi.org/10.1186/1471-2148-13-80openalex-snapshot
A Southern Hemisphere origin for campanulid angiosperms, with traces of the break-up of Gondwana
inferred← citeshttps://doi.org/10.1186/1471-2148-6-36openalex-snapshot
A survey of nuclear ribosomal internal transcribed spacer substitution rates across angiosperms: an approximate molecular clock with life history effects.
inferred← citeshttps://doi.org/10.1186/s40693-014-0024-0openalex-snapshot
Robles in Lagunas de Epulauquen, Argentina: previous and recent evidence of their distinctive character
inferred← citeshttps://doi.org/10.1371/journal.pbio.0030014openalex-snapshot
Relaxed Molecular Clock Provides Evidence for Long-Distance Dispersal of Nothofagus (Southern Beech)
inferred← citeshttps://doi.org/10.1371/journal.pone.0172708openalex-snapshot
Phylogenetic relationships of Vepris (Rutaceae) inferred from chloroplast, nuclear, and morphological data
inferred← citeshttps://doi.org/10.1515/acpa-2016-0017openalex-snapshot
Pollen morphology of Nothofagus (Nothofagaceae, Fagales) and its phylogenetic significance
inferred← citeshttps://doi.org/10.1515/sg-2004-0043openalex-snapshot
SSR Markers for Analysing South American Nothofagus Species
inferred← citeshttps://doi.org/10.1515/sg-2008-0013openalex-snapshot
Primer Note: A New Set of Highly Polymorphic Nuclear Microsatellite Markers for Nothofagus nervosa and Related South American Species
inferred← citeshttps://doi.org/10.18195/issn.0313-122x.68.2005.053-102openalex-snapshot
The character of the New Zealand land snail fauna and communities: some evolutionary and ecological perspectives
inferred← citeshttps://doi.org/10.2307/1224719openalex-snapshot
Biogeography of Nothofagus supports the sequence of Gondwana break‐up
inferred← citeshttps://doi.org/10.2307/2419549openalex-snapshot
Phylogenetic Systematics of Ipomoea (Convolvulaceae) Based on ITS and Waxy Sequences
inferred← citeshttps://doi.org/10.2307/2446139openalex-snapshot
Phylogenetic analyses of “higher” Hamamelididae based on plastid sequence data
inferred← citeshttps://doi.org/10.2307/2656726openalex-snapshot
Phylogenetic relationships of functionally dioecious FICUS (Moraceae) based on ribosomal DNA sequences and morphology
inferred← citeshttps://doi.org/10.2307/2656981openalex-snapshot
Phylogeny and evolution of the Betulaceae as inferred from DNA sequences, morphology, and paleobotany
inferred← citeshttps://doi.org/10.2307/2657072openalex-snapshot
Phylogeny and patterns of floral diversity in the genus Piper (Piperaceae)
inferred← citeshttps://doi.org/10.2307/2666677openalex-snapshot
Phylogenetic Relationships among Acanthaceae: Evidence from Two Genomes
inferred← citeshttps://doi.org/10.25959/23210015openalex-snapshot
Range-wide chloroplast DNA phylogeographies of three widespread Australian cool temperate rainforest plants
inferred← citeshttps://doi.org/10.26021/8061openalex-snapshot
Biogeography of Nothofagus subgenus Fuscospora in the South Island of New Zealand inferred from chloroplast DNA.
inferred← citeshttps://doi.org/10.3103/s009545270705009xopenalex-snapshot
Origins of native vascular plants of antarctica: Comments from a historical phytogeography viewpoint
inferred← citeshttps://doi.org/10.31055/1851.2372.v46.n1-2.53701openalex-snapshot
Distribución natural de Nothofagus alpina y Nothofagus obliqua (Nothofagaceae) en Argentina, dos especies de primera importancia forestal de los bosques templados norpatagónicos
inferred← citeshttps://doi.org/10.3389/fpls.2018.01073openalex-snapshot
Evolution of Climatic Related Leaf Traits in the Family Nothofagaceae
inferred← citeshttps://doi.org/10.3417/2011083openalex-snapshot
Catalog and Literature Guide for Cretaceous and Cenozoic Vascular Plants of the New World1
inferred← citeshttps://doi.org/10.3724/sp.j.1227.2011.00104openalex-snapshot
A cladistic scenario of Southern Pacific bio-geographical history based on Nothofagus dis-persal and vicariance analysis
inferred← citeshttps://doi.org/10.3732/ajb.1400379openalex-snapshot
Evolutionary divergence of leaf width and its correlates
inferred← citeshttps://doi.org/10.3732/ajb.91.11.1863openalex-snapshot
Phylogenetic relationships of Malvatheca (Bombacoideae and Malvoideae; Malvaceae sensu lato) as inferred from plastid DNA sequences
inferred← citeshttps://doi.org/10.3732/ajb.92.4.667openalex-snapshot
Phylogenetic relationships among New Caledonian Sapotaceae (Ericales): molecular evidence for generic polyphyly and repeated dispersal
inferred← citeshttps://doi.org/10.3732/ajb.94.8.1382openalex-snapshot
Bud and growth‐unit structure in seedlings and saplings of Nothofagus alpina (Nothofagaceae)
inferred← citeshttps://doi.org/10.3852/10-048openalex-snapshot
Cophylogeny and biogeography of the fungal parasite Cyttaria and its host Nothofagus, southern beech
inferred← citeshttps://doi.org/10.4067/s0717-66432014000200015openalex-snapshot
Chromosome number of two Chilean species of Nothofagus (Nothofagaceae)
inferred← citeshttps://doi.org/10.4067/s0717-92002005000200004openalex-snapshot
Evidencia morfológica e isoenzimática de hibridación natural entre Nothofagus antarctica y N. pumilio en el noroeste patagónico
inferred← citeshttps://doi.org/10.4067/s0717-92002006000100001openalex-snapshot
El uso de marcadores genéticos en el género Nothofagus con especial referencia a raulí y roble
inferred← citeshttps://doi.org/10.4067/s0717-92002010000100002openalex-snapshot
Descripción de posibles híbridos naturales entre Nothofagus pumilio y N. antarctica en Patagonia Sur (Argentina)
inferred← citeshttps://doi.org/10.4067/s0717-92002015000300015openalex-snapshot
Descripción morfológica y viabilidad del polen de Nothofagus nervosa (Nothofagaceae)
inferred← citeshttps://doi.org/10.4067/s0717-92002016000300016openalex-snapshot
Searching for molecular insight on hybridization in Nothofagus spp. forests at Lagunas de Epulauquen, Argentina
inferred← citeshttps://doi.org/10.4067/s0718-686x2008000100005openalex-snapshot
NOTHOFAGUS BETULOIDES (MIRB.) OERST 1871 (FAGALES: NOTHOFAGACEAE) FORESTS IN SOUTHERN PATAGONIA AND TIERRA DEL FUEGO
inferred← citeshttps://doi.org/10.7717/peerj.6779openalex-snapshot
Hybrid identification in Nothofagus subgenus using high resolution melting with ITS and trnL approach
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