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Molecular phylogeny ofNothofagus (Nothofagaceae) based on theatpB-rbcL intergenic spacer of the chloroplast DNA

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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/mpev.1994.1004openalex-snapshot
Molecular Phylogeny of Families Related to Celastrales Based on rbcL 5′ Flanking Sequences
inferredcites →https://doi.org/10.1007/978-1-4020-6754-9_12413openalex-snapshot
PAUP (phylogenetic analysis using parsimony)
inferredcites →https://doi.org/10.1007/978-90-481-8748-5_9openalex-snapshot
Nothofagus, Key Genus in Plant Geography
inferredcites →https://doi.org/10.1007/bf00937437openalex-snapshot
Ribosomal and chloroplast DNA restriction site mutations and the radiation ofRobinsonia (Asteraceae: Senecioneae) on the Juan Fernandez Islands
inferredcites →https://doi.org/10.1007/bf02344248openalex-snapshot
Allozyme diversity and the evolution ofSymplocos (Symplocaceae) on the Bonin (Ogasawara) Islands
inferredcites →https://doi.org/10.1007/bf02344310openalex-snapshot
Phylogenetic relationships inCrossostylis (Rhizophoraceae) inferred from restriction site variation of chloroplast DNA
inferredcites →https://doi.org/10.1007/bf02491263openalex-snapshot
Allozyme diversity and the evolution ofCrepidiastrum (Compositae) on the Bonin (Ogasawara) Islands
inferredcites →https://doi.org/10.1016/0034-6667(94)90096-5openalex-snapshot
Nothofagus smithtonensis (Nothofagaceae), a new macrofossil species from Oligocene sediments in northwest Tasmania, Australia, and its phylogenetic significance
inferredcites →https://doi.org/10.1016/0040-1951(74)90044-4openalex-snapshot
Implications of continental drift to the earth sciences. 1
inferredcites →https://doi.org/10.1038/170127a0openalex-snapshot
Identification of Tertiary Pollen Grains with those of New Guinea and New Caledonian Beeches
inferredcites →https://doi.org/10.1071/bt8310077openalex-snapshot
Cyttaria (Cyttariales): Coevolution with Nothofagus, and Evolutionary Relationship to the Boedijnopezizeae (Pezizales, Sarcoscyphaceae)
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/10.1080/00167617808729012openalex-snapshot
The southwest pacific area during the last 90 million years
inferredcites →https://doi.org/10.1080/0028825x.1979.10426911openalex-snapshot
Leaf vernation in Nothofagus
inferredcites →https://doi.org/10.1080/0028825x.1993.10419490openalex-snapshot
Recent colonisation by Nothofagus fusca at Cass, Canterbury
inferredcites →https://doi.org/10.1080/03115517808527776openalex-snapshot
Evolution of the Australian flora and vegetation through the Tertiary: evidence from pollen
inferredcites →https://doi.org/10.1097/00010694-195303000-00016openalex-snapshot
Pollen Morphology and Plant Taxonomy
inferredcites →https://doi.org/10.1098/rspb.1960.0056openalex-snapshot
Southern Hemisphere Mesozoic and Tertiary Podocarpaceae and Fagaceae and their palaeogeographic significance
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.1095-8339.1991.tb00200.xopenalex-snapshot
Tertiary Nothofagus (Fagaceae) macrofossils from Tasmania and Antarctica and their bearing on the evolution of the genus
inferredcites →https://doi.org/10.1111/j.1096-0031.1995.tb00002.xopenalex-snapshot
NOTHOFAGUSAND PACIFIC BIOGEOGRAPHY
inferredcites →https://doi.org/10.1111/j.1502-3931.1987.tb00766.xopenalex-snapshot
Origins and Evolution of the Antarctic Biota
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/10.1111/j.1558-5646.1986.tb00565.xopenalex-snapshot
ADAPTIVE RADIATION IN THE HAWAIIAN SILVERSWORD ALLIANCE (COMPOSITAE‐MADIINAE). II. CYTOGENETICS OF ARTIFICIAL AND NATURAL HYBRIDS
inferredcites →https://doi.org/10.1126/science.176.4042.1379openalex-snapshot
Plate Tectonics and Australasian Paleobiogeography
inferredcites →https://doi.org/10.1126/science.95.2455.69openalex-snapshot
Continental Drift and Plant Distribution
inferredcites →https://doi.org/10.2307/1218054openalex-snapshot
Taxonomy, Phytogeography and Evolution
inferredcites →https://doi.org/10.2307/1222143openalex-snapshot
STUDIES IN ANNONACEAE. VIII. A CLADISTIC ANALYSIS OF TETRAMERANTHUS
inferredcites →https://doi.org/10.2307/1222145openalex-snapshot
A MOLECULAR EVOLUTIONARY CLOCK FOR ANGIOSPERMS
inferredcites →https://doi.org/10.2307/1547303openalex-snapshot
Adiantum capillus-veneris Chloroplast DNA Clone Bank: As Useful Heterologous Probes in the Systematics of the Leptosporangiate Ferns
inferredcites →https://doi.org/10.2307/2395021openalex-snapshot
Angiosperm Biogeography and Past Continental Movements
inferredcites →https://doi.org/10.2307/2395196openalex-snapshot
Historical Biogeography and Earth History: Perspectives for a Future Synthesis
inferredcites →https://doi.org/10.2307/2399846openalex-snapshot
Phylogenetics of Seed Plants: An Analysis of Nucleotide Sequences from the Plastid Gene rbcL
inferredcites →https://doi.org/10.2307/2419268openalex-snapshot
Allozyme Divergence and the Evolution of Dendroseris (Compositae: Lactuceae) on the Juan Fernandez Islands
inferredcites →https://doi.org/10.2307/2419735openalex-snapshot
Evolution of the Genus Dendroseris (Asteraceae: Lactuceae) on the Juan Fernandez Islands: Evidence from Chloroplast and Ribosomal DNA
inferredcites →https://doi.org/10.2307/2446156openalex-snapshot
Systematics of Nothofagus (Nothofagaceae) based on rDNA spacer sequences (ITS): taxonomic congruence with morphology and plastid sequences
inferredcites →https://doi.org/10.2307/2846036openalex-snapshot
The New Zealand Flora-Entirely Long-Distance Dispersal?
inferredcites →https://doi.org/10.2307/4103125openalex-snapshot
An Interesting New Species of Nothofagus from New Guinea (Fagaceae)
inferredcites →https://doi.org/10.2307/4113753openalex-snapshot
Coevolution and Systematics
inferredcites →https://doi.org/10.2307/4115792openalex-snapshot
On the Evolution of Cupules in the Fagaceae
inferredcites →https://doi.org/10.5169/seals-65253openalex-snapshot
Morphologie und Klassifikation neu-caledonischer Arten der Fagaceen-Gattung Trisyngyne
inferredcites →https://doi.org/10.5281/zenodo.16384697openalex-snapshot
Taxonomy of some Cretaceous spores and pollen grains from Eastern Australia
inferredcites →https://doi.org/10.5962/bhl.part.27154openalex-snapshot
Results of the Archbold expeditions Papuan nothofagus
inferredcites →https://doi.org/10.5962/bhl.part.8319openalex-snapshot
Additional note on Nothofagus
inferredcites →https://doi.org/10.5962/p.296678openalex-snapshot
Revision of Nothofagus in New Caledonia

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.146.1.1zenodo-depositor-declared
Revised circumscription of Nothofagus and recognition of the segregate genera Fuscospora, Lophozonia, and Trisyngyne (Nothofagaceae)
inferred← citeshttps://doi.org/10.11646/phytotaxa.159.2.1zenodo-depositor-declared
Phylogenetics, character evolution and a subgeneric revision of the genus Pelargonium (Geraniaceae)
inferred← citeshttps://doi.org/10.11646/phytotaxa.197.1.2zenodo-depositor-declared
A new species and new section of Viola (Violaceae) from Guangdong, China
inferred← citeshttps://doi.org/10.1002/tax.12133openalex-snapshot
Origin and evolution of Atriplex (Amaranthaceae s.l.) in the Americas: Unexpected insights from South American species
inferred← citeshttps://doi.org/10.1006/clad.2000.0146openalex-snapshot
Nothofagus Biogeography Revisited with Special Emphasis on the Enigmatic Distribution of Subgenus Brassospora in New Caledonia
inferred← citeshttps://doi.org/10.1007/978-3-642-56849-7_14openalex-snapshot
Molecular Systematics: 1997–1999
inferred← citeshttps://doi.org/10.1007/bf01177723openalex-snapshot
Polymorphism analysis of Fagaceae and DNA-based identification ofFagus species grown in Japan based on therbcL gene
inferred← citeshttps://doi.org/10.1007/pl00013885openalex-snapshot
Molecular Phylogeny of Magnolia (Magnoliaceae) Inferred from cpDNA Sequences and Evolutionary Divergence of the Floral Scents
inferred← citeshttps://doi.org/10.1007/s00122-001-0824-xopenalex-snapshot
Comparison of ISSR and RAPD markers to characterize three Chilean Nothofagus species
inferred← citeshttps://doi.org/10.1007/s00606-002-0214-0openalex-snapshot
Ontogeny of pistillate flowers and inflorescences in Nothofagus subgenus Lophozonia (Nothofagaceae)
inferred← citeshttps://doi.org/10.1007/s11557-012-0832-zopenalex-snapshot
Erysiphe havrylenkoana and E. prunastri var. japonica: a new species and a new variety of Erysiphe sect. Uncinula (Erysiphaceae, Ascomycota)
inferred← citeshttps://doi.org/10.1007/s11557-021-01696-7openalex-snapshot
A new species, phylogeny, and a worldwide key of the edible wood decay Fistulina (Agaricales)
inferred← citeshttps://doi.org/10.1016/j.jsames.2021.103250openalex-snapshot
Macroevolutionary changes in the fossil plant record: Key examples from the Cretaceous-Paleogene of Patagonia, Argentina
inferred← citeshttps://doi.org/10.1016/j.ympev.2003.10.009openalex-snapshot
Phylogeny of Panax using chloroplast trnC–trnD intergenic region and the utility of trnC–trnD in interspecific studies of plants
inferred← citeshttps://doi.org/10.1016/j.ympev.2009.08.008openalex-snapshot
Evidence of chloroplast capture in South American Nothofagus (subgenus Nothofagus, Nothofagaceae)
inferred← citeshttps://doi.org/10.1016/s0031-9422(02)00666-0openalex-snapshot
Taxonomic significance of flavonoid variation in temperate species of Nothofagus
inferred← citeshttps://doi.org/10.1023/a:1015158408227openalex-snapshot
Molecular Phylogeny of Genus Vigna Subgenus Ceratotropis Based on rDNA ITS and atpB-rbcL Intergenic Spacer of cpDNA Sequences
inferred← citeshttps://doi.org/10.1071/bt00027openalex-snapshot
Most parsimonious areagrams versus fossils: the case of Nothofagus (Nothofagaceae)
inferred← citeshttps://doi.org/10.1071/bt03179openalex-snapshot
Bark anatomy of Nothofagus species (Nothofagaceae) indigenous to the Andean–Patagonian forest, Argentina
inferred← citeshttps://doi.org/10.1071/bt04155openalex-snapshot
Phytogeography and climate analysis of Nothofagus subgenus Brassospora in New Guinea and New Caledonia
inferred← citeshttps://doi.org/10.1071/bt04215openalex-snapshot
Genetic diversity and regional identity in the Australian remnant Nothofagus moorei
inferred← citeshttps://doi.org/10.1071/sb02033openalex-snapshot
Nothofagus kiandrensis (Nothofagaceae subgenus Brassospora ), a new macrofossil leaf species from Miocene sediments at Kiandra, New South Wales
inferred← citeshttps://doi.org/10.1071/sb99010openalex-snapshot
Ancestral area analysis of Nothofagus (Nothofagaceae) and its congruence with the fossil record
inferred← citeshttps://doi.org/10.1079/cabicompendium.36454openalex-snapshot
Nothofagus nitida
inferred← citeshttps://doi.org/10.1080/0028825x.2014.960946openalex-snapshot
Relationships, gene flow and species boundaries among New Zealand Fuscospora (Nothofagaceae: southern beech)
inferred← citeshttps://doi.org/10.1080/08912963.2022.2150549openalex-snapshot
Ancient Antarctica: the early evolutionary history ofNothofagus
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
inferred← citeshttps://doi.org/10.1086/375423openalex-snapshot
Evolution of Hedera (the Ivy Genus, Araliaceae): Insights from Chloroplast DNA Data
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.2005.3219openalex-snapshot
Not so ancient: the extant crown group of Nothofagus represents a post-Gondwanan radiation
inferred← citeshttps://doi.org/10.1098/rstb.2004.1528openalex-snapshot
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/j.0014-3820.2003.tb00256.xopenalex-snapshot
PHYLOGEOGRAPHIC STRUCTURE AND CRYPTIC SPECIATION IN THE TRANS-ANTARCTIC MOSS PYRRHOBRYUM MNIOIDES
inferred← citeshttps://doi.org/10.1111/j.1759-6831.2010.00102.xopenalex-snapshot
Infrageneric relationships of Korean Viola based on eight chloroplast markers
inferred← citeshttps://doi.org/10.11113/jt.v59.1591openalex-snapshot
Phylogeny of Subtribe Aeridinae (Orchidaceae) Inferred from DNA Sequences Data : Advanced Analyses Including Australasian Genera
inferred← citeshttps://doi.org/10.1515/acpa-2016-0017openalex-snapshot
Pollen morphology of Nothofagus (Nothofagaceae, Fagales) and its phylogenetic significance
inferred← citeshttps://doi.org/10.18942/bunrui.kj00004649674openalex-snapshot
ニューカレドニアにおけるNepenthes vieillardii Hook. f. (Nepenthaceae)の種内分化(学位論文紹介)
inferred← citeshttps://doi.org/10.2307/1224719openalex-snapshot
Biogeography of Nothofagus supports the sequence of Gondwana break‐up
inferred← citeshttps://doi.org/10.2307/2446478openalex-snapshot
Phylogenetic relationships within Araucariaceae based on rbcL gene sequences
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/10.3724/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.0800129openalex-snapshot
Genetic diversity and geographical structure of the pitcher plant Nepenthes vieillardii in New Caledonia: A chloroplast DNA haplotype analysis
inferred← citeshttps://doi.org/10.3852/08-030openalex-snapshot
Molecular data do not support a southern hemisphere base of Nothofagus powdery mildews
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/s0717-92002006000100001openalex-snapshot
El uso de marcadores genéticos en el género Nothofagus con especial referencia a raulí y roble
inferred← citeshttps://doi.org/10.4202/app.00493.2018openalex-snapshot
Phylogenetic relationships and time-calibration of the South American fossils and extant species of southern beeches (Nothofagus)
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