On the public citation graph
A Tale of Two Hyper-diversities: Diversification dynamics of the two largest families of lichenized fungi
0 signed · 107 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/mpev.2000.0856openalex-snapshot
Molecular Evidence for the Diversification of Extant Lichens in the Late Cretaceous and Tertiary
inferredcites →https://doi.org/10.1007/978-3-540-87407-2_16openalex-snapshot
Lichen-Forming Fungi and Their Photobionts
inferredcites →https://doi.org/10.1007/s13225-011-0135-8openalex-snapshot
A new classification for the family Graphidaceae (Ascomycota: Lecanoromycetes: Ostropales)
inferredcites →https://doi.org/10.1016/j.jpba.2010.04.013openalex-snapshot
HPLC isolation of antioxidant constituents from Xanthoparmelia spp.
inferredcites →https://doi.org/10.1016/j.revpalbo.2006.05.004openalex-snapshot
Progressive substitution of a subtropical forest for a temperate one during the middle Miocene climate cooling in Central Europe according to palynological data from cores Tengelic-2 and Hidas-53 (Pannonian Basin, Hungary)
inferredcites →https://doi.org/10.1016/j.ympev.2006.11.029openalex-snapshot
Testing morphology-based hypotheses of phylogenetic relationships in Parmeliaceae (Ascomycota) using three ribosomal markers and the nuclear RPB1 gene
inferredcites →https://doi.org/10.1016/s0098-8472(99)00034-9openalex-snapshot
Physiological responses of the lichen Xanthoparmelia mexicana to oxidative stress of SO2
inferredcites →https://doi.org/10.1038/nature06588openalex-snapshot
An early Cenozoic perspective on greenhouse warming and carbon-cycle dynamics
inferredcites →https://doi.org/10.1038/nature11631openalex-snapshot
The global diversity of birds in space and time
inferredcites →https://doi.org/10.1038/nature12872openalex-snapshot
Three keys to the radiation of angiosperms into freezing environments
inferredcites →https://doi.org/10.1038/ncomms2958openalex-snapshot
Rates of speciation and morphological evolution are correlated across the largest vertebrate radiation
inferredcites →https://doi.org/10.1073/pnas.0400938101openalex-snapshot
Body plan evolution of ascomycetes, as inferred from an RNA polymerase II phylogeny
inferredcites →https://doi.org/10.1073/pnas.0811087106openalex-snapshot
Nine exceptional radiations plus high turnover explain species diversity in jawed vertebrates
inferredcites →https://doi.org/10.1080/14772000.2014.905506openalex-snapshot
High frequency of character transformations is phylogenetically structured within the lichenized fungal family Graphidaceae (Ascomycota: Ostropales)
inferredcites →https://doi.org/10.1086/682061openalex-snapshot
A Unique Trait Associated with Increased Diversification in a Hyperdiverse Family of Tropical Lichen–Forming Fungi
inferredcites →https://doi.org/10.1093/sysbio/syp001openalex-snapshot
A Phylogenetic Estimation of Trophic Transition Networks for Ascomycetous Fungi: Are Lichens Cradles of Symbiotrophic Fungal Diversification?
inferredcites →https://doi.org/10.1093/sysbio/syp020openalex-snapshot
The Ascomycota Tree of Life: A Phylum-wide Phylogeny Clarifies the Origin and Evolution of Fundamental Reproductive and Ecological Traits
inferredcites →https://doi.org/10.1093/sysbio/syu025openalex-snapshot
Analysis and Visualization of Complex Macroevolutionary Dynamics: An Example from Australian Scincid Lizards
inferredcites →https://doi.org/10.1098/rspb.2009.1176openalex-snapshot
Life history influences rates of climatic niche evolution in flowering plants
inferredcites →https://doi.org/10.1111/2041-210x.12091openalex-snapshot
Unifying fossils and phylogenies for comparative analyses of diversification and trait evolution
inferredcites →https://doi.org/10.1111/j.1468-0459.2010.00374.xopenalex-snapshot
Growth of crustose lichens: a review
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01835.xopenalex-snapshot
Photoprotection in an ecological context: the remarkable complexity of thermal energy dissipation
inferredcites →https://doi.org/10.1111/j.1502-3931.1977.tb00604.xopenalex-snapshot
Early vascular land plants: proof and conjecture
inferredcites →https://doi.org/10.1111/j.1756-1051.2012.00008.xopenalex-snapshot
A review of the lichen family Parmeliaceae – history, phylogeny and current taxonomy
inferredcites →https://doi.org/10.1111/nph.13553openalex-snapshot
Evolution of complex symbiotic relationships in a morphologically derived family of lichen‐forming fungi
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.7770775openalex-snapshot
Multiple Origins of Lichen Symbioses in Fungi Suggested by SSU rDNA Phylogeny
inferredcites →https://doi.org/10.1130/1052-5173(2004)014<0019:carcaa>2.0.co;2openalex-snapshot
CO2 as a primary driver of Phanerozoic climate: Reply
inferredcites →https://doi.org/10.1130/1052-5173(2004)014<4:caapdo>2.0.co;2openalex-snapshot
CO2 as a primary driver of Phanerozoic climate
inferredcites →https://doi.org/10.11646/phytotaxa.189.1.4openalex-snapshot
One hundred and seventy-five new species of Graphidaceae: closing the gap or a drop in the bucket?
inferredcites →https://doi.org/10.11646/phytotaxa.189.1.6openalex-snapshot
Revisiting the phylogeny of Ocellularieae, the second largest tribe within Graphidaceae (lichenized Ascomycota: Ostropales)
inferredcites →https://doi.org/10.1186/1471-2148-7-214openalex-snapshot
BEAST: Bayesian evolutionary analysis by sampling trees
inferredcites →https://doi.org/10.1186/1471-2148-8-257openalex-snapshot
Accelerated evolutionary rates in tropical and oceanic parmelioid lichens (Ascomycota)
inferredcites →https://doi.org/10.1371/journal.pone.0028161openalex-snapshot
Origin and Diversification of Major Clades in Parmelioid Lichens (Parmeliaceae, Ascomycota) during the Paleogene Inferred by Bayesian Analysis
inferredcites →https://doi.org/10.1371/journal.pone.0083115openalex-snapshot
Understanding Phenotypical Character Evolution in Parmelioid Lichenized Fungi (Parmeliaceae, Ascomycota)
inferredcites →https://doi.org/10.1371/journal.pone.0089543openalex-snapshot
Automatic Detection of Key Innovations, Rate Shifts, and Diversity-Dependence on Phylogenetic Trees
inferredcites →https://doi.org/10.1639/0747-9859-25.4.85openalex-snapshot
Lichens of the Boulder Mountain Plateau, Wayne County, Utah, USA
inferredcites →https://doi.org/10.3114/sim.2008.61.11openalex-snapshot
A rock-inhabiting ancestor for mutualistic and pathogen-rich fungal lineages
inferredcites →https://doi.org/10.3170/2008-8-18433openalex-snapshot
The influence of tree age and microhabitat quality on the occurrence of crustose lichens associated with old oaks
inferredcites →https://doi.org/10.3417/2009143openalex-snapshot
Angiosperms Helped Put the Rain in the Rainforests: The Impact of Plant Physiological Evolution on Tropical Biodiversity1
inferredcites →https://doi.org/10.3732/ajb.1200258openalex-snapshot
Diversification of the newly recognized lichen‐forming fungal lineage Montanelia (Parmeliaceae, Ascomycota) and its relation to key geological and climatic events
inferredcites →https://doi.org/10.3732/ajb.91.10.1614openalex-snapshot
The origin and diversification of angiosperms
inferredcites →https://doi.org/10.3897/mycokeys.6.3482openalex-snapshot
A molecular phylogeny of Graphidaceae (Ascomycota, Lecanoromycetes, Ostropales) including 428 species
inferredcites →https://doi.org/10.5479/si.0081024x.74openalex-snapshot
A Synopsis of the Lichen Genus Xanthoparmelia (Vainio) Hale (Ascomycotina, Parmeliaceae)
inferredcites →https://doi.org/10.5962/bhl.title.115446openalex-snapshot
Natural selection and tropical nature : essays on descriptive and theoretical biology
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/s13127-016-0273-7zenodo-depositor-declared
Evaluation of traditionally circumscribed species in the lichen-forming genus Usnea, section Usnea (Parmeliaceae, Ascomycota) using a six-locus dataset
inferred← citeshttps://doi.org/10.11646/megataxa.1.1.16zenodo-depositor-declared
Three challenges to contemporaneous taxonomy from a licheno-mycological perspective
inferred← citeshttps://doi.org/10.11646/phytotaxa.664.1.3zenodo-depositor-declared
Molecular studies of Allographa effusosoredica sp. nov. (Graphidaceae) along with its Trentepohlia photobiont and a comprehensive checklist for Indian Allographa
inferred← citeshttps://doi.org/10.1002/ece3.5056openalex-snapshot
Genome streamlining via complete loss of introns has occurred multiple times in lichenized fungal mitochondria
inferred← citeshttps://doi.org/10.1007/978-3-319-29532-9_2openalex-snapshot
2 Ecological Biogeography of Lichen-Forming Fungi
inferred← citeshttps://doi.org/10.1007/s00300-021-02976-4openalex-snapshot
Contrasting variation patterns in Austroplaca hookeri and Rusavskia elegans (Teloschistaceae, lichenized Ascomycota) in maritime Antarctica
inferred← citeshttps://doi.org/10.1007/s00606-023-01862-2openalex-snapshot
The monotypic genus Flavocetraria and two new genera: Cladocetraria and Foveolaria, in the cetrarioid core
inferred← citeshttps://doi.org/10.1007/s10531-019-01925-2openalex-snapshot
Global species richness prediction for Pyrenulaceae (Ascomycota: Pyrenulales), the last of the “big three” most speciose tropical microlichen families
inferred← citeshttps://doi.org/10.1007/s11557-026-02141-3openalex-snapshot
Revisiting Allographa (Graphidales, Graphidaceae) from the Western Ghats, India
inferred← citeshttps://doi.org/10.1007/s13127-016-0320-4openalex-snapshot
Using multi-locus sequence data for addressing species boundaries in commonly accepted lichen-forming fungal species
inferred← citeshttps://doi.org/10.1007/s13225-015-0346-5openalex-snapshot
Fungal diversity notes 111–252—taxonomic and phylogenetic contributions to fungal taxa
inferred← citeshttps://doi.org/10.1007/s13225-016-0366-9openalex-snapshot
Fungal diversity notes 253–366: taxonomic and phylogenetic contributions to fungal taxa
inferred← citeshttps://doi.org/10.1007/s13225-017-0379-zopenalex-snapshot
Using a temporal phylogenetic method to harmonize family- and genus-level classification in the largest clade of lichen-forming fungi
inferred← citeshttps://doi.org/10.1007/s13225-018-0407-7openalex-snapshot
Phylogenomic analysis of 2556 single-copy protein-coding genes resolves most evolutionary relationships for the major clades in the most diverse group of lichen-forming fungi
inferred← citeshttps://doi.org/10.1007/s13225-022-00498-wopenalex-snapshot
Predicting global numbers of teleomorphic ascomycetes
inferred← citeshttps://doi.org/10.1016/b978-0-12-800049-6.00249-3openalex-snapshot
Lichen-Forming Fungi, Diversification of
inferred← citeshttps://doi.org/10.1016/b978-0-443-15750-9.00109-9openalex-snapshot
Lichen-Forming Fungi, Diversification of
inferred← citeshttps://doi.org/10.1016/j.funbio.2016.06.001openalex-snapshot
Hidden diversity before our eyes: Delimiting and describing cryptic lichen-forming fungal species in camouflage lichens (Parmeliaceae, Ascomycota)
inferred← citeshttps://doi.org/10.1016/j.funbio.2020.07.007openalex-snapshot
Low genetic differentiation between apotheciate Usnea florida and sorediate Usnea subfloridana (Parmeliaceae, Ascomycota) based on microsatellite data
inferred← citeshttps://doi.org/10.1016/j.funbio.2025.101710openalex-snapshot
Diversification and spatio-temporal evolution of Cladoniaceae (Lecanorales, Ascomycota), a widespread family of lichen-forming fungi
inferred← citeshttps://doi.org/10.1016/j.orggeochem.2023.104588openalex-snapshot
Aliphatic hydrocarbons in the lichen class Lecanoromycetes and their potential use as chemotaxonomic indicators and biomarkers
inferred← citeshttps://doi.org/10.1016/j.ympev.2016.03.030openalex-snapshot
Cryptic diversity and symbiont interactions in rock-posy lichens
inferred← citeshttps://doi.org/10.1016/j.ympev.2018.01.012openalex-snapshot
High diversity, high insular endemism and recent origin in the lichen genus Sticta (lichenized Ascomycota, Peltigerales) in Madagascar and the Mascarenes
inferred← citeshttps://doi.org/10.1016/j.ympev.2018.10.035openalex-snapshot
New insights into the Usnea cornuta aggregate (Parmeliaceae, lichenized Ascomycota): Molecular analysis reveals high genetic diversity correlated with chemistry
inferred← citeshttps://doi.org/10.1016/j.ympev.2021.107380openalex-snapshot
Phylogenetic revision of the lichenized family Gomphillaceae (Ascomycota: Graphidales) suggests post-K–Pg boundary diversification and phylogenetic signal in asexual reproductive structures
inferred← citeshttps://doi.org/10.1016/j.ympev.2022.107543openalex-snapshot
Interpreting phylogenetic conflict: Hybridization in the most speciose genus of lichen-forming fungi
inferred← citeshttps://doi.org/10.1016/j.ympev.2025.108407openalex-snapshot
Speciation continuum in non-model organisms: Revisiting the species-pair concept in lichens
inferred← citeshttps://doi.org/10.1017/s0024282918000191openalex-snapshot
Historical biogeography of the lichenized fungal genusHypotrachyna(Parmeliaceae, Ascomycota): insights into the evolutionary history of a pantropical clade
inferred← citeshttps://doi.org/10.1017/s0024282918000233openalex-snapshot
Assessing phylogeny and historical biogeography of the largest genus of lichen-forming fungi, Xanthoparmelia (Parmeliaceae, Ascomycota)
inferred← citeshttps://doi.org/10.1017/s0024282919000392openalex-snapshot
GraphisandAllographa(lichenized Ascomycota:Graphidaceae) in Sri Lanka, with six new species and a biogeographical comparison investigating a potential signature of the ‘biotic ferry’ species interchange
inferred← citeshttps://doi.org/10.1017/s0024282923000555openalex-snapshot
Multi-locus phylogeny of Bryoria reveals recent diversification and unexpected diversity in section Divaricatae
inferred← citeshttps://doi.org/10.1017/s1755691017000111openalex-snapshot
Diversity of lichen-associated filamentous fungi preserved in European Paleogene amber
inferred← citeshttps://doi.org/10.1038/s41598-019-44881-1openalex-snapshot
Accelerated diversifications in three diverse families of morphologically complex lichen-forming fungi link to major historical events
inferred← citeshttps://doi.org/10.1038/s41598-022-14970-9openalex-snapshot
Lichen speciation is sparked by a substrate requirement shift and reproduction mode differentiation
inferred← citeshttps://doi.org/10.1038/s41598-024-74937-wopenalex-snapshot
A shift in substrate requirement might cause speciation of the lichenized fungi, Varicellaria hemisphaerica and V. lactea (Pertusariales, Ascomycota)
inferred← citeshttps://doi.org/10.1073/pnas.2001913117openalex-snapshot
The macroevolutionary dynamics of symbiotic and phenotypic diversification in lichens
inferred← citeshttps://doi.org/10.1080/07352689.2019.1650517openalex-snapshot
Stop the Abuse of Time! Strict Temporal Banding is not the Future of Rank-Based Classifications in Fungi (Including Lichens) and Other Organisms
inferred← citeshttps://doi.org/10.1080/14772000.2016.1226977openalex-snapshot
Neogene diversification in the temperate lichen-forming fungal genus Parmelia (Parmeliaceae, Ascomycota)
inferred← citeshttps://doi.org/10.1093/aob/mcy182openalex-snapshot
Thirty clues to the exceptional diversification of flowering plants
inferred← citeshttps://doi.org/10.1093/botlinnean/box022openalex-snapshot
Understanding disjunct distribution patterns in lichen-forming fungi: insights from Parmelina (Parmeliaceae: Ascomycota)
inferred← citeshttps://doi.org/10.1093/femsec/fiab072openalex-snapshot
Macroecological diversification and convergence in a clade of keystone symbionts
inferred← citeshttps://doi.org/10.1101/2021.08.02.454570openalex-snapshot
New insights into the earlier evolutionary history of epiphytic macrolichens
inferred← citeshttps://doi.org/10.1111/evo.13099openalex-snapshot
Is the switch to an ectomycorrhizal state an evolutionary key innovation in mushroom‐forming fungi? A case study in the Tricholomatineae (Agaricales)
inferred← citeshttps://doi.org/10.1111/evo.13364openalex-snapshot
Frequent and parallel habitat transitions as driver of unbounded radiations in the Cape flora
inferred← citeshttps://doi.org/10.1111/jbi.13554openalex-snapshot
Parallel Miocene dispersal events explain the cosmopolitan distribution of the Hypogymnioid lichens
inferred← citeshttps://doi.org/10.1111/jpy.12994openalex-snapshot
Trentepohlialean Algae (Trentepohliales, Ulvophyceae) Show Preference to Selected Mycobiont Lineages in Lichen Symbioses
inferred← citeshttps://doi.org/10.1139/gen-2015-0189openalex-snapshot
Barcoding lichen-forming fungi using 454 pyrosequencing is challenged by artifactual and biological sequence variation
inferred← citeshttps://doi.org/10.1186/s43008-020-00051-xopenalex-snapshot
Using target enrichment sequencing to study the higher-level phylogeny of the largest lichen-forming fungi family: Parmeliaceae (Ascomycota)
inferred← citeshttps://doi.org/10.1371/journal.pone.0146537openalex-snapshot
An Integrative Approach for Understanding Diversity in the Punctelia rudecta Species Complex (Parmeliaceae, Ascomycota)
inferred← citeshttps://doi.org/10.1371/journal.pone.0161031openalex-snapshot
Hidden Genetic Diversity in an Asexually Reproducing Lichen Forming Fungal Group
inferred← citeshttps://doi.org/10.1639/0007-2745-119.1.107openalex-snapshot
Recent literature on lichens—240
inferred← citeshttps://doi.org/10.1639/0007-2745-123.2.127openalex-snapshot
The new genus Jocatoa (Lecanoromycetes: Graphidaceae) and new insights into subfamily Redonographoideae
inferred← citeshttps://doi.org/10.3158/2158-5520-16.9.1openalex-snapshot
Assembling a Taxonomic Monograph of Tribe Wirthiotremateae (Lichenized Ascomycota: Ostropales: Graphidaceae)
inferred← citeshttps://doi.org/10.3372/jb.2015-2016.en.1openalex-snapshot
Diversity is our mission. BGBM Annual Report 2015-2016
inferred← citeshttps://doi.org/10.3389/fmicb.2018.00283openalex-snapshot
Multiple, Distinct Intercontinental Lineages but Isolation of Australian Populations in a Cosmopolitan Lichen-Forming Fungal Taxon, Psora decipiens (Psoraceae, Ascomycota)
inferred← citeshttps://doi.org/10.3390/jof12090654openalex-snapshot
Optimal Partitioning for Molecular Phylogenetic Inference and Generic Delimitation in the Cetrarioid Core Group (Parmeliaceae, Ascomycota)
inferred← citeshttps://doi.org/10.3390/jof8080826openalex-snapshot
A New Cryptic Lineage in Parmeliaceae (Ascomycota) with Pharmacological Properties
inferred← citeshttps://doi.org/10.3390/jof9010099openalex-snapshot
Reference-Based RADseq Unravels the Evolutionary History of Polar Species in ‘the Crux Lichenologorum’ Genus Usnea (Parmeliaceae, Ascomycota)
inferred← citeshttps://doi.org/10.3897/mycokeys.36.22548openalex-snapshot
Different diversification histories in tropical and temperate lineages in the ascomycete subfamily Protoparmelioideae (Parmeliaceae)
inferred← citeshttps://doi.org/10.3989/ajbm.2564openalex-snapshot
Diversity of Xanthoparmelia (Parmeliaceae) species in Mexican xerophytic scrub vegetation, evidenced by molecular, morphological and chemistry data
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.