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Chloroplast DNA variation and the phylogeny ofAsplenium sect.Hymenasplenium (Aspleniaceae) in the New World tropics
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1537-2197.1989.tb15154.xopenalex-snapshot
CHROMOSOMES AND SYSTEMATICS OF ASPLENIUM SECT. HYMENASPLENIUM (ASPLENIACEAE)
inferredcites →https://doi.org/10.1002/j.1537-2197.1992.tb14613.xopenalex-snapshot
MATERNAL INHERITANCE OF THE CHLOROPLAST AND MITOCHONDRIAL GENOMES IN CHEILANTHOID FERNS
inferredcites →https://doi.org/10.1007/bf00314885openalex-snapshot
Chloroplast DNA from Adiantum capillus-veneris L., a fern species (Adiantaceae); clone bank, physical map and unusual gene localization in comparison with angiosperm chloroplast DNA
inferredcites →https://doi.org/10.1007/bf02488082openalex-snapshot
Chemotaxonomic studies ofAsplenium sect.Hymenasplenium (Aspleniaceae)
inferredcites →https://doi.org/10.1007/bf02489409openalex-snapshot
Stelar structure ofAsplenium obtusifolium and its allied species in the New World tropics, with comparison to the Asian members ofAsplenium sect.Hymenasplenium
inferredcites →https://doi.org/10.1007/bf02491261openalex-snapshot
Structure of cDNA clones for the small subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase from a fern (Asplenium cataractarum rosenstock, aspleniaceae), and its comparison with those of various seed plants
inferredcites →https://doi.org/10.1007/bf02491264openalex-snapshot
The systematic position ofAsplenium cardiophyllum (Aspleniaceae)
inferredcites →https://doi.org/10.1016/0003-2697(83)90418-9openalex-snapshot
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
inferredcites →https://doi.org/10.1016/0031-9422(80)85004-7openalex-snapshot
Deviations from michaelis-menten behaviour of plant glutamate dehydrogenase with ammonium as variable substrate
inferredcites →https://doi.org/10.1016/s0031-9422(00)97683-0openalex-snapshot
d-2-Aminopimelic acid and trans-3,4-dehydro-d-2-aminopimelic acid from Asplenium unilaterale
inferredcites →https://doi.org/10.21829/abm5.1989.1122openalex-snapshot
Mickel, J. T. & J. M. Beitel. 1988. Pteridophyte Flora of Oaxaca, México. Memoirs of the New York Botanical Garden 46: 1-568
inferredcites →https://doi.org/10.2307/1546462openalex-snapshot
Diplazium delitescens and the Neotropical Species of Asplenium sect. Hymenasplenium
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/10.2307/2399279openalex-snapshot
Chloroplast DNA Variation and Plant Phylogeny
inferredcites →https://doi.org/10.2307/2399820openalex-snapshot
Monograph of the Neotropical Species of Asplenium Sect. Hymenasplenium (Aspleniaceae)
inferredcites →https://doi.org/10.5962/bhl.title.140155openalex-snapshot
Über den Bau von Angiopteris
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.344.3.6zenodo-depositor-declared
Prodromus of a fern flora for Bolivia. XXIX. Aspleniaceae
inferred← citeshttps://doi.org/10.11646/phytotaxa.374.4.1zenodo-depositor-declared
Validation of Hymenasplenium laterepens (Aspleniaceae): evidence from morphology and molecular analyses
inferred← citeshttps://doi.org/10.11646/phytotaxa.595.1.10zenodo-depositor-declared
Hymenasplenium hovenkampii (Aspleniaceae), a new bipinnatisect fern species from Lesser Sunda Islands of Indonesia
inferred← citeshttps://doi.org/10.1007/978-1-4615-5419-6_19openalex-snapshot
Phylogenetic Studies of Extant Pteridophytes
inferred← citeshttps://doi.org/10.1007/978-3-642-55819-1_14openalex-snapshot
Systematics of the Pteridophytes
inferred← citeshttps://doi.org/10.1007/978-3-642-59940-8_15openalex-snapshot
Systematics of the Pteridophytes
inferred← citeshttps://doi.org/10.1007/bf02344351openalex-snapshot
Systematics and evolutionary biology of the fern genusHymenasplenium (Aspleniaceae)
inferred← citeshttps://doi.org/10.1007/bf02506806openalex-snapshot
Allozyme diversity ofPittosporum (Pittosporaceae) on the Bonin (Ogasawara) Islands
inferred← citeshttps://doi.org/10.1007/bf02763405openalex-snapshot
Origin and evolution of endemic plants of the Bonin (Ogasawara) Islands
inferred← citeshttps://doi.org/10.1007/s00606-016-1359-6openalex-snapshot
Phylogenetic relationships of two Cuban spleenworts with unusual morphology: Asplenium (Schaffneria) nigripes and Asplenium pumilum (Aspleniaceae, leptosporangiate ferns)
inferred← citeshttps://doi.org/10.1016/j.ympev.2018.05.021openalex-snapshot
A global plastid phylogeny uncovers extensive cryptic speciation in the fern genus Hymenasplenium (Aspleniaceae)
inferred← citeshttps://doi.org/10.1016/s0305-1978(98)00065-9openalex-snapshot
Low isozymic differentiation among five species of the Macrozamia heteromera group (Zamiaceae)
inferred← citeshttps://doi.org/10.1093/aob/mcz124openalex-snapshot
Hymenasplenium volubile: documentation of its gametophytes and the first record of a hemiepiphyte in the Aspleniaceae
inferred← citeshttps://doi.org/10.1111/1755-6724.13353openalex-snapshot
Asplenium sanshuiense sp. nov.: the Lowest Latitude Fossil Record of the Genus
inferred← citeshttps://doi.org/10.1111/j.1442-1984.2012.00383.xopenalex-snapshot
Ecological and genetic differentiation in Persea boninensis (Lauraceae) endemic to the Bonin (Ogasawara) Islands
inferred← citeshttps://doi.org/10.1111/jse.12223openalex-snapshot
State of the art and perspectives on neotropical fern and lycophyte systematics
inferred← citeshttps://doi.org/10.1111/jse.13194openalex-snapshot
Phylogeny and biogeography of the fern genus Hymenasplenium (Aspleniaceae), with special reference to island speciation
inferred← citeshttps://doi.org/10.11110/kjpt.2013.43.2.90openalex-snapshot
A new record of fern species from Korean flora: Asplenium septentrionale (L.) Hoffm. (Aspleniaceae)
inferred← citeshttps://doi.org/10.11110/kjpt.2015.45.4.362openalex-snapshot
Two new and one unrecorded natural hybrids between Asplenium ruprechtii and related taxa (Aspleniaceae)
inferred← citeshttps://doi.org/10.11110/kjpt.2019.49.2.127openalex-snapshot
Exploring natural hybridizations among Asplenium ruprechtii and related taxa in Korea
inferred← citeshttps://doi.org/10.11646/phytotaxa.19.1.2openalex-snapshot
A linear sequence of extant families and genera of lycophytes and ferns
inferred← citeshttps://doi.org/10.14522/darwiniana.2014.11.497openalex-snapshot
El género Hymenasplenium (Aspleniaceae) en Argentina
inferred← citeshttps://doi.org/10.1600/036364404774195476openalex-snapshot
Chloroplast Phylogeny of Asplenioid Ferns based on rbcL and trnL-F Spacer Sequences (Polypodiidae, Aspleniaceae) and its Implications for Biogeography
inferred← citeshttps://doi.org/10.1600/036364421x16231782047451openalex-snapshot
A Reassessment of the Little-Known Amazonian Fern Diplazium praestans Based on Molecular and Morphological Evidence
inferred← citeshttps://doi.org/10.1640/0002-8444(2001)091[0197:ppolta]2.0.co;2openalex-snapshot
Phylogenetic Placements of Loxoscaphe thecifera (Aspleniaceae) and Actiniopteris radiata (Pteridaceae) Based on Analysis ofrbcLNucleotide Sequences
inferred← citeshttps://doi.org/10.1640/0002-8444-101.4.265openalex-snapshot
The Genus Hymenasplenium (Aspleniaceae) in Cuba, Including New Combinations for the Neotropical Species
inferred← citeshttps://doi.org/10.2307/25065903openalex-snapshot
Fern phylogeny inferred from 400 leptosporangiate species and three plastid genes
inferred← citeshttps://doi.org/10.3897/phytokeys.211.90363openalex-snapshot
Molecular and morphological evidence reveals a new fern species of Hymenasplenium (Aspleniaceae) from south and southwestern China
inferred← citeshttps://doi.org/10.7717/peerj.18667openalex-snapshot
Comparative analysis of Hymenasplenium (Aspleniaceae) chloroplast genomes from China
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