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A Unique Trait Associated with Increased Diversification in a Hyperdiverse Family of Tropical Lichen–Forming Fungi

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Outgoing claims: the papers this work cites, builds on, or argues with.

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A new classification for the family Graphidaceae (Ascomycota: Lecanoromycetes: Ostropales)
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Parallel evolution and phenotypic divergence in lichenized fungi: A case study in the lichen-forming fungal family Graphidaceae (Ascomycota: Lecanoromycetes: Ostropales)
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The global diversity of birds in space and time
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The latitudinal species richness gradient in New World woody angiosperms is consistent with the tropical conservatism hypothesis
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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)
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Latitudinal Gradients in Species Diversity: A Review of Concepts
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The Latitudinal Gradient in Geographical Range: How so Many Species Coexist in the Tropics
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Escalation of Plant Defense: Do Latex and Resin Canals Spur Plant Diversification?
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Bayesian Phylogenetics with BEAUti and the BEAST 1.7
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Spurring plant diversification: are floral nectar spurs a key innovation?
inferredcites →https://doi.org/10.1111/ele.12251openalex-snapshot
Phylogenetic approaches for studying diversification
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General latitudinal gradient of biodiversity is reversed in ectomycorrhizal fungi
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LATITUDINAL VARIATIONS IN ORGANIC DIVERSITY
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Diversitree: comparative phylogenetic analyses of diversification in R
inferredcites →https://doi.org/10.1126/science.1130880openalex-snapshot
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inferredcites →https://doi.org/10.1127/nova.hedwigia/64/1997/147openalex-snapshot
Ingvariella, a new genus in the Thelotremataceae (lichenized Ascomycotina)
inferredcites →https://doi.org/10.1146/annurev-ecolsys-110512-135800openalex-snapshot
Diversity-Dependence, Ecological Speciation, and the Role of Competition in Macroevolution
inferredcites →https://doi.org/10.1146/annurev.ecolsys.34.012103.144032openalex-snapshot
Latitudinal Gradients of Biodiversity: Pattern, Process, Scale, and Synthesis
inferredcites →https://doi.org/10.1163/9789004337862_lgbo_com_161117openalex-snapshot
Princeton University Press
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/10.12705/622.10openalex-snapshot
Phylogenetic study of Diploschistes (lichen–forming Ascomycota: Ostropales: Graphidaceae), based on morphological, chemical, and molecular data
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.0089543openalex-snapshot
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inferredcites →https://doi.org/10.1371/journal.pone.0097722openalex-snapshot
C4 Photosynthesis Promoted Species Diversification during the Miocene Grassland Expansion
inferredcites →https://doi.org/10.1890/070020openalex-snapshot
Changing lenses to assess biodiversity: patterns of species richness in sub-Antarctic plants and implications for global conservation
inferredcites →https://doi.org/10.2307/1940797openalex-snapshot
Adaptive Radiation in Sticklebacks: Size, Shape, and Habitat Use Efficiency
inferredcites →https://doi.org/10.3732/ajb.1200548openalex-snapshot
Journey from the West: Did tropical Graphidaceae (lichenized Ascomycota: Ostropales) evolve from a saxicolous ancestor along the American Pacific coast?
inferredcites →https://doi.org/10.3852/10-287openalex-snapshot
Expansion of the Stictidaceae by the addition of the saxicolous lichen-forming genusIngvariella
inferredcites →https://doi.org/10.3897/mycokeys.6.3482openalex-snapshot
A molecular phylogeny of Graphidaceae (Ascomycota, Lecanoromycetes, Ostropales) including 428 species
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Columbia University Press

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Three new species of Graphidaceae (lichenized Ascomycota) from the semi-arid region of northeast Brazil
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/10.1016/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.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/10.1038/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/srep10028openalex-snapshot
A Tale of Two Hyper-diversities: Diversification dynamics of the two largest families of lichenized fungi
inferred← citeshttps://doi.org/10.1639/0007-2745-119.1.107openalex-snapshot
Recent literature on lichens—240
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Mission grüne Vielfalt. BGBM Jahresbericht 2015-2016
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.2022.831450openalex-snapshot
Host Shift Speciation of the Ectomycorrhizal Genus Suillus (Suillineae, Boletales) and Biogeographic Comparison With Its Host Pinaceae
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