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Origin and subdivision of Plagiochila (Jungermanniidae: Plagiochilaceae) in tropical Africa based on evidence from nuclear and chloroplast DNA sequences and morphology
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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.2000.0786openalex-snapshot
Phylogenetic Relationships, Morphological Incongruence, and Geographic Speciation in the Fontinalaceae (Bryophyta)
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Testing Morphological Concepts of Orders of Pleurocarpous Mosses (Bryophyta) Using Phylogenetic Reconstructions Based on TRNL-TRNF and RPS4 Sequences
inferredcites →https://doi.org/10.1006/mpev.2001.1067openalex-snapshot
Phylogeny and Morphological Evolution of the Amblystegiaceae (Bryopsida)
inferredcites →https://doi.org/10.1007/bf00045016openalex-snapshot
Environmental history of East Africa
inferredcites →https://doi.org/10.1007/bf00985374openalex-snapshot
Systematics ofPlagiochila sect.Glaucescentes Carl (Hepaticae) from tropical America: A morphological and chemotaxonomical approach
inferredcites →https://doi.org/10.1007/s00299-001-0399-7openalex-snapshot
Regeneration and molecular characterization of intergeneric somatic hybrids between Citrus reticulata and Poncirus trifoliata
inferredcites →https://doi.org/10.1007/s00382-003-0341-5openalex-snapshot
Low-latitude control of interhemispheric sea-surface temperature contrast in the tropical Atlantic over the past 21�kyears: the possible role of SE trade winds
inferredcites →https://doi.org/10.1007/s00606-004-0220-5openalex-snapshot
Distribution and synonymy of Plagiochila punctata (Taylor) Taylor, with hypotheses on the evolutionary history of Plagiochila sect. Arrectae (Plagiochilaceae, Hepaticae)
inferredcites →https://doi.org/10.1007/s00606-004-0221-4openalex-snapshot
Cryptic speciation in Herbertus (Herbertaceae, Jungermanniopsida): Range and morphology of Herbertus sendtneri inferred from nrITS sequences
inferredcites →https://doi.org/10.1007/s006060200006openalex-snapshot
Plagiochila virginica A.Evans rather than P. dubia Lindenb. & Gottsche occurs in Macaronesia; placement in sect. Contiguae Carl is supported by ITS sequences of nuclear ribosomal DNA
inferredcites →https://doi.org/10.1016/j.ode.2004.01.001openalex-snapshot
nrDNA internal transcribed spacer data reveal that R.M. Schust. (Marchantiophyta: Jungermanniales) is a member of sect. Carl
inferredcites →https://doi.org/10.1016/s0367-2530(04)70082-1openalex-snapshot
Geomolecular divergence in the Gondwanan dendroid Symphyogyna complex (Pallaviciniaceae, Hepaticophytina, Bryophyta)Studies in austral temperate rain forest bryophytes 22
inferredcites →https://doi.org/10.1016/s1290-0796(02)85003-9openalex-snapshot
Lectotypification and synonymy of Plagiochila sect. Vagae Lindenb. (Hepaticae)
inferredcites →https://doi.org/10.1016/s1290-0796(02)85006-4openalex-snapshot
ITS sequences of nuclear ribosomal DNA support the generic placement and the disjunct range of Plagiochila (Adelanthus) carringtonii
inferredcites →https://doi.org/10.1029/2000jc000507openalex-snapshot
Tropical monsoons around Africa: Stability of El Niño–Southern Oscillation associations and links with continental climate
inferredcites →https://doi.org/10.1029/2003gl017557openalex-snapshot
Reconstruction of SE trade‐wind intensity based on sea‐surface temperature gradients in the Southeast Atlantic over the last 25 kyr
inferredcites →https://doi.org/10.1029/2003gl017867openalex-snapshot
Near surface westerly wind jet in the Atlantic ITCZ
inferredcites →https://doi.org/10.1038/346347a0openalex-snapshot
Temperature and rainfall estimates for the past 40,000 years in equatorial Africa
inferredcites →https://doi.org/10.1038/nature01500openalex-snapshot
African vegetation controlled by tropical sea surface temperatures in the mid-Pleistocene period
inferredcites →https://doi.org/10.1046/j.1365-2699.2001.00530.xopenalex-snapshot
Biogeographic patterns and cryptic speciation in bryophytes
inferredcites →https://doi.org/10.1046/j.1365-2699.2001.00531.xopenalex-snapshot
Geographic distributions of homosporous ferns: does dispersal obscure evidence of vicariance?
inferredcites →https://doi.org/10.1046/j.1365-2699.2003.00916.xopenalex-snapshot
Biogeography ofPlagiochila(Hepaticae): natural species groups span several floristic kingdoms
inferredcites →https://doi.org/10.1055/s-2003-44716openalex-snapshot
Reinstatement of Chiastocaulon Carl (Plagiochilaceae), Based on Evidence from Nuclear Ribosomal ITS and Chloroplast Gene rps4 Sequences
inferredcites →https://doi.org/10.1055/s-2004-817801openalex-snapshot
Molecular Phylogeography of the Moss Tortula muralis Hedw. (Pottiaceae) Based on Chloroplast rps4 Gene Sequence Data
inferredcites →https://doi.org/10.1071/bt00023openalex-snapshot
The breakup history of Gondwana and its impact on pre-Cenozoic floristic provincialism
inferredcites →https://doi.org/10.1073/pnas.102175899openalex-snapshot
Laurasian migration explains Gondwanan disjunctions: Evidence from Malpighiaceae
inferredcites →https://doi.org/10.1080/0028825x.2001.9512745openalex-snapshot
Recognised species of Plagiochila in Australasia and some island groups of the Pacific Ocean
inferredcites →https://doi.org/10.1080/0028825x.2002.9512784openalex-snapshot
Molecular generic classification of the Hypopterygiaceae (Bryopsida), with the description of a new genus, Arbusculohypopterygium gen. nov. studies in austral temperate rain forest bryophytes 10
inferredcites →https://doi.org/10.1086/383334openalex-snapshot
Plant Dispersal across the Tropical Atlantic by Wind and Sea Currents
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/nar/gkg155openalex-snapshot
The complete nucleotide sequence of the hornwort (Anthoceros formosae) chloroplast genome: insight into the earliest land plants
inferredcites →https://doi.org/10.1093/oso/9780198542919.003.0004openalex-snapshot
Bryophyte distribution patterns
inferredcites →https://doi.org/10.1093/sysbio/45.4.524openalex-snapshot
Testing for Phylogenetic Conflict Among Molecular Data Sets in the Tribe Triticeae (Gramineae)
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb00256.xopenalex-snapshot
PHYLOGEOGRAPHIC STRUCTURE AND CRYPTIC SPECIATION IN THE TRANS-ANTARCTIC MOSS PYRRHOBRYUM MNIOIDES
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.1095-8339.2004.00340.xopenalex-snapshot
Intercontinental distribution of Plagiochila corrugata (Plagiochilaceae, Hepaticae) inferred from nrDNA ITS sequences and morphology
inferredcites →https://doi.org/10.1126/science.1095210openalex-snapshot
Wind as a Long-Distance Dispersal Vehicle in the Southern Hemisphere
inferredcites →https://doi.org/10.1127/0029-5035/2004/0078-0057openalex-snapshot
Molecular circumscription and relationships of selected Gondwanan species of Haplomitrium (Calobryales, Haplomitriopsida, Hepaticophytina)
inferredcites →https://doi.org/10.1127/0029-5035/2004/0079-0497openalex-snapshot
Plagiochila stricta Lindenb. new to Madeira Morphological and molecular evidence
inferredcites →https://doi.org/10.1127/nova.hedwigia/67/1998/289openalex-snapshot
Molecular divergence patterns and infrageneric relationship of Monoclea (Monocleales, Hepaticae). Studies in austral temperate rain forest bryophytes
inferredcites →https://doi.org/10.1127/nova.hedwigia/68/1999/511openalex-snapshot
Redescription and synonymy of Plagiochila aerea Taylor 1846 (Hepaticae), first described as Lycopodium pinnatum by Lamarck 1792
inferredcites →https://doi.org/10.1127/nova.hedwigia/70/2000/161openalex-snapshot
A revision of Plagiochila sect. Crispatae and sect. Hypnoides (Hepaticae) in the Neotropics. I. Plagiochila disticha, P. montagnei and P. raddiana
inferredcites →https://doi.org/10.1130/0016-7606(2000)112<1091:uhotca>2.0.co;2openalex-snapshot
Uplift history of the Central and Northern Andes: A review
inferredcites →https://doi.org/10.1130/0016-7606(2000)112<1091:uhotca>2.3.co;2openalex-snapshot
Uplift history of the Central and Northern Andes: A review
inferredcites →https://doi.org/10.1130/0091-7613(2001)029<0195:mpecit>2.0.co;2openalex-snapshot
Mid-Pleistocene environmental change in tropical Africa began as early as 1.05 Ma
inferredcites →https://doi.org/10.1179/006813868804146953openalex-snapshot
The Hepaticae and Anthocerotae of North America East of the Hundredth Meridian
inferredcites →https://doi.org/10.1179/tbbs.1962.4.2.254openalex-snapshot
African Hepatics XV.Plagiochilain Tropical Africa
inferredcites →https://doi.org/10.1639/0007-2745(2000)103[0625:proaam]2.0.co;2openalex-snapshot
Phylogenetic Relationships ofAsterella(Aytoniaceae, Marchantiopsida) Inferred from Chloroplast DNA Sequences
inferredcites →https://doi.org/10.1639/0007-2745(2001)104[0350:prhapk]2.0.co;2openalex-snapshot
Plagiochila rutilans(Hepaticae): A Poorly Known Species from Tropical America
inferredcites →https://doi.org/10.1639/0007-2745(2002)105[0189:tspopm]2.0.co;2openalex-snapshot
The Systematic Position of Plagiochila moritziana, P. trichostoma, and P. deflexa Based on ITS Sequence Variation of Nuclear Ribosomal DNA, Morphology, and Lipophilic Secondary Metabolites
inferredcites →https://doi.org/10.1639/0007-2745(2002)105[0363:pmamef]2.0.co;2openalex-snapshot
Phytochemical, Morphological, and Molecular Evidence for the Occurrence of the Neotropical Liverwort Plagiochila stricta in the Canary Islands, New to Macaronesia
inferredcites →https://doi.org/10.1639/0007-2745(2004)107[28:mmapef]2.0.co;2openalex-snapshot
Molecular, Morphological, and Phytochemical Evidence for a Broad Species Concept of Plagiochila bifaria (Hepaticae)
inferredcites →https://doi.org/10.1639/0007-2745(2004)107[489:scotna]2.0.co;2openalex-snapshot
Sectional Classification of the North American Plagiochila (Hepaticae, Plagiochilaceae)
inferredcites →https://doi.org/10.2307/1555022openalex-snapshot
The Systematic Status of Plagiochila sects. Bidentes Carl and Caducilobae Inoue (Hepaticae) Inferred from nrDNA ITS Sequences
inferredcites →https://doi.org/10.2307/1797381openalex-snapshot
Biogeography and Ecology in South America
inferredcites →https://doi.org/10.2307/2419632openalex-snapshot
ITS Sequences and the Phylogeny of the Genus Robinsonia (Asteraceae)
inferredcites →https://doi.org/10.2307/25027887openalex-snapshot
Plagiochila (Hepaticae, Plagiochilaceae) in China
inferredcites →https://doi.org/10.2307/3239540openalex-snapshot
Die Arttypen und die Systematische Gliederung der Gattung Plagiochila Dum
inferredcites →https://doi.org/10.2307/3243487openalex-snapshot
The Moss Adelothecium bogotense in Continental Africa, with a Review of Its World Range
inferredcites →https://doi.org/10.2307/3647332openalex-snapshot
The systematic status of Plagiochila sects. Bidentes Carl and Caducilobae Inoue (Hepaticae) inferred from nrDNA ITS sequences
inferredcites →https://doi.org/10.2307/3667735openalex-snapshot
Le genre Plagiochila (Dum.) Dum. (Hepaticae) a Madagascar et aux Mascareignes, principalement d'apres les recoltes de M. Onraedt
inferredcites →https://doi.org/10.3732/ajb.90.4.540openalex-snapshot
Intercontinental Mediterranean disjunct mosses: morphological and molecular patterns
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.195.2.8zenodo-depositor-declared
Validation of Plagiochila fracta nomen nudum (Jungermanniopsida). East African bryophytes XXXI.
inferred← citeshttps://doi.org/10.11646/phytotaxa.208.1.8zenodo-depositor-declared
Notes on Early Land Plants Today. 69. Circumscription of Plagiochilaceae (Marchantiophyta) with a preliminary infrageneric subdivision of Plagiochila
inferred← citeshttps://doi.org/10.11646/phytotaxa.319.1.2zenodo-depositor-declared
Molecular, morphological, and biogeographic perspectives on the classification of Acrobolboideae (Acrobolbaceae, Marchantiophyta)
inferred← citeshttps://doi.org/10.11646/phytotaxa.601.3.5zenodo-depositor-declared
Climatic conditions may structure the distribution of Syzygiella rubricaulis (Nees) Steph., a disjunct and high elevation species
inferred← citeshttps://doi.org/10.5252/cryptogamie-bryologie2022v43a5zenodo-depositor-declared
The Genus Plagiochila (Dumort.) Dumort. (Marchantiophyta) in Madagascar
inferred← citeshttps://doi.org/10.1002/ece3.2656openalex-snapshot
Geographical structure, narrow species ranges, and C enozoic diversification in a pantropical clade of epiphyllous leafy liverworts
inferred← citeshttps://doi.org/10.1007/s00606-006-0411-3openalex-snapshot
Goodbye or welcome Gondwana? – insights into the phylogenetic biogeography of the leafy liverwort Plagiochila with a description of Proskauera, gen. nov. (Plagiochilaceae, Jungermanniales)
inferred← citeshttps://doi.org/10.1007/s00606-006-0463-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00606-013-0860-4openalex-snapshot
The Bromeliaceae tank dweller Bromeliophila (Lejeuneaceae, Porellales) is a member of the Cyclolejeunea-Prionolejeunea clade
inferred← citeshttps://doi.org/10.1007/s13127-015-0258-yopenalex-snapshot
A phylogeny of Lophocoleaceae-Plagiochilaceae-Brevianthaceae and a revised classification of Plagiochilaceae
inferred← citeshttps://doi.org/10.1016/j.ympev.2006.02.013openalex-snapshot
Budding speciation and neotropical origin of the Azorean endemic liverwort, Leptoscyphus azoricus
inferred← citeshttps://doi.org/10.1016/j.ympev.2007.05.005openalex-snapshot
A phylogeny of Porella (Porellaceae, Jungermanniopsida) based on nuclear and chloroplast DNA sequences
inferred← citeshttps://doi.org/10.1016/j.ympev.2008.12.021openalex-snapshot
Molecular insights into the phylogeny and subgeneric classification of Frullania Raddi (Frullaniaceae, Porellales)
inferred← citeshttps://doi.org/10.1016/j.ympev.2009.05.032openalex-snapshot
DNA taxonomy, cryptic speciation and diversification of the Neotropical-African liverwort, Marchesinia brachiata (Lejeuneaceae, Porellales)
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Phylogeny of the leafy liverwort Ptilidium: Cryptic speciation and shared haplotypes between the Northern and Southern Hemispheres
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inferred← citeshttps://doi.org/10.1016/j.ympev.2012.07.009openalex-snapshot
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inferred← citeshttps://doi.org/10.1017/cbo9780511754807.012openalex-snapshot
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inferred← citeshttps://doi.org/10.1017/cbo9780511754807.013openalex-snapshot
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inferred← citeshttps://doi.org/10.1017/cbo9780511844270.015openalex-snapshot
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inferred← citeshttps://doi.org/10.1071/sb16038openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/0028825x.2017.1318756openalex-snapshot
The New Zealand endemic Plagiochila caducifolia is a disjunct population of Plagiochila spinulosa (Plagiochilaceae: Jungermanniopsida)
inferred← citeshttps://doi.org/10.1086/508023openalex-snapshot
Testing Hypotheses on Species Delimitations and Disjunctions in the Liverwort Bryopteris (Jungermanniopsida: Lejeuneaceae)
inferred← citeshttps://doi.org/10.1111/bij.12200openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/boj.12279openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/boj.12495openalex-snapshot
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Phylogeographic analyses reveal distinct lineages of the liverworts Metzgeria furcata (L.) Dumort. and Metzgeria conjugata Lindb. (Metzgeriaceae) in Europe and North America
inferred← citeshttps://doi.org/10.1111/j.1365-2699.2006.01623.xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1111/j.1469-185x.2009.00111.xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1111/j.1558-5646.2008.00567.xopenalex-snapshot
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