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Photobiont flexibility in the lichen Protoparmeliopsis muralis as revealed by ITS rDNA analyses
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inferred← citeshttps://doi.org/10.11646/phytotaxa.383.2.3zenodo-depositor-declared
Evaluation of diagnostic chemical and morphological characters in five Parmelia species (Parmeliaceae, lichenized Ascomycota) with special emphasis on the thallus pruinosity
inferred← citeshttps://doi.org/10.1002/gcb4.70000openalex-snapshot
Future Range Shifts and Diversity Patterns of Antarctic Lecideoid Lichens Under Climate Change Scenarios
inferred← citeshttps://doi.org/10.1007/978-1-4614-8736-4_4openalex-snapshot
Photobiont Diversity in Indian Cladonia Lichens, with Special Emphasis on the Geographical Patterns
inferred← citeshttps://doi.org/10.1007/978-3-642-30826-0_15openalex-snapshot
15 The Symbiotic Phenotype of Lichen-Forming Ascomycetes and Their Endo- and Epibionts
inferred← citeshttps://doi.org/10.1007/978-981-97-9873-5_2openalex-snapshot
Soil Algae Symbioses: Raising the Curtain of an Ancient Play
inferred← citeshttps://doi.org/10.1007/s00248-009-9584-yopenalex-snapshot
Joint Dispersal Does Not Imply Maintenance of Partnerships in Lichen Symbioses
inferred← citeshttps://doi.org/10.1007/s00300-013-1295-7openalex-snapshot
Photobiont selectivity for lichens and evidence for a possible glacial refugium in the Ross Sea Region, Antarctica
inferred← citeshttps://doi.org/10.1007/s00792-024-01355-1openalex-snapshot
Diversity of lichen mycobionts and photobionts and their relationships in the Ny-Ålesund region (Svalbard, High Arctic)
inferred← citeshttps://doi.org/10.1007/s12229-009-9028-xopenalex-snapshot
Asymmetric Co-evolution in the Lichen Symbiosis Caused by a Limited Capacity for Adaptation in the Photobiont
inferred← citeshttps://doi.org/10.1007/s13199-010-0060-8openalex-snapshot
Morphological and phylogenetic study of algal partners associated with the lichen-forming fungus Tephromela atra from the Mediterranean region
inferred← citeshttps://doi.org/10.1007/s13199-015-0321-7openalex-snapshot
The role of symbiosis in the transition of some eukaryotes from aquatic to terrestrial environments
inferred← citeshttps://doi.org/10.1007/s13199-015-0346-yopenalex-snapshot
Lichen photobionts of the rocky outcrops of Karadag massif (Crimean Peninsula)
inferred← citeshttps://doi.org/10.1007/s13199-016-0458-zopenalex-snapshot
Phylogenetic signal of photobiont switches in the lichen genus Pseudocyphellaria s. l. follows a Brownian motion model
inferred← citeshttps://doi.org/10.1007/s13199-025-01036-3openalex-snapshot
The plurality of photobionts within single lichen thalli
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2009.11.002openalex-snapshot
Photobiont diversity in lichens from metal-rich substrata based on ITS rDNA sequences
inferred← citeshttps://doi.org/10.1016/j.flora.2010.02.001openalex-snapshot
Site factors controlling epiphytic lichen abundance in northern coniferous forests
inferred← citeshttps://doi.org/10.1016/j.funeco.2018.11.005openalex-snapshot
Relationships between mycobiont identity, photobiont specificity and ecological preferences in the lichen genus Peltigera (Ascomycota) in Estonia (northeastern Europe)
inferred← citeshttps://doi.org/10.1016/j.mycres.2007.04.008openalex-snapshot
Trouble with lichen: the re-evaluation and re-interpretation of thallus form and fruit body types in the molecular era
inferred← citeshttps://doi.org/10.1016/j.ympev.2010.05.013openalex-snapshot
Multiple origins of high reciprocal symbiotic specificity at an intercontinental spatial scale among gelatinous lichens (Collemataceae, Lecanoromycetes)
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/10.1017/cbo9780511974878.011openalex-snapshot
Biogeography and phylogeography of lichen fungi and their photobionts
inferred← citeshttps://doi.org/10.1017/s0024282909008111openalex-snapshot
Genetically divergent algae shape an epiphytic lichen community on Jack Pine in Manitoba
inferred← citeshttps://doi.org/10.1017/s0024282912000217openalex-snapshot
Diversity ofRamalina sinensisand its photobiont in local populations
inferred← citeshttps://doi.org/10.1017/s0024282912000291openalex-snapshot
Genetic diversity of photobionts in Antarctic lecideoid lichens from an ecological view point
inferred← citeshttps://doi.org/10.1017/s002428291200059xopenalex-snapshot
In vitro culturing and resynthesis of the mycobiont Protoparmeliopsis muralis with algal bionts
inferred← citeshttps://doi.org/10.1017/s002428291300042xopenalex-snapshot
Development of microsatellite markers in Protoparmeliopsis muralis (lichenized Ascomycete) – a common lichen species
inferred← citeshttps://doi.org/10.1017/s0024282913000546openalex-snapshot
Genetic diversity of sterile culturedTrebouxiaphotobionts associated with the lichen-forming fungusXanthoria parietinavisualized with RAPD-PCR fingerprinting techniques
inferred← citeshttps://doi.org/10.1017/s0024282913000819openalex-snapshot
Green-algal photobiont diversity (Trebouxia spp.) in representatives of Teloschistaceae (Lecanoromycetes, lichen-forming ascomycetes)
inferred← citeshttps://doi.org/10.1017/s0024282916000232openalex-snapshot
Photobiont associations in co-occurring umbilicate lichens with contrasting modes of reproduction in coastal Norway
inferred← citeshttps://doi.org/10.1017/s0024282921000335openalex-snapshot
Lichen algae: the photosynthetic partners in lichen symbioses
inferred← citeshttps://doi.org/10.1017/s0024282926101364openalex-snapshot
Bound by ammonia: pollution constrains Cetraria sepincola at the margin of its Central European range
inferred← citeshttps://doi.org/10.1017/s0954102016000286openalex-snapshot
Bacterial communities in Antarctic lichens
inferred← citeshttps://doi.org/10.1038/s41598-018-23219-3openalex-snapshot
Photobiont switching causes changes in the reproduction strategy and phenotypic dimorphism in the Arthoniomycetes
inferred← citeshttps://doi.org/10.1038/s41598-021-02940-6openalex-snapshot
Macroclimatic conditions as main drivers for symbiotic association patterns in lecideoid lichens along the Transantarctic Mountains, Ross Sea region, Antarctica
inferred← citeshttps://doi.org/10.1038/s41598-024-70667-1openalex-snapshot
The application of haplotypes instead of species-level ranks modifies the interpretation of ecological preferences in lichen symbiont interactions in Parmelia
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/10.1080/00275514.2020.1813486openalex-snapshot
Lichen-forming fungi in postindustrial habitats involve alternative photobionts
inferred← citeshttps://doi.org/10.1093/aob/mcu146openalex-snapshot
Photobiont selectivity leads to ecological tolerance and evolutionary divergence in a polymorphic complex of lichenized fungi
inferred← citeshttps://doi.org/10.1093/femsec/fiac008openalex-snapshot
The guilds in green algal lichens—an insight into the life of terrestrial symbiotic communities
inferred← citeshttps://doi.org/10.1093/femsec/fiaf096openalex-snapshot
The diverse world within: age-dependent photobiont diversity in the lichen Protoparmeliopsis muralis
inferred← citeshttps://doi.org/10.1101/2022.03.30.485788openalex-snapshot
The interplay between habitat fragmentation and life traits affects specialization in lichen symbioses
inferred← citeshttps://doi.org/10.1111/1365-2745.14229openalex-snapshot
The combined effects of habitat fragmentation and life history traits on specialisation in lichen symbioses
inferred← citeshttps://doi.org/10.1111/1462-2920.70379openalex-snapshot
Symbiotic Versatility in Action: Trebouxia Diversity Expands the Niche of the Lichen Xanthoria parietina
inferred← citeshttps://doi.org/10.1111/1574-6941.12120openalex-snapshot
The symbiotic playground of lichen thalli - a highly flexible photobiont association in rock-inhabiting lichens
inferred← citeshttps://doi.org/10.1111/1758-2229.13105openalex-snapshot
Microbial community associated with the crustose lichen Rhizocarpon geographicum L. ( DC .) living on oceanic seashore: A large source of diversity revealed by using multiple isolation methods
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2010.04993.xopenalex-snapshot
Population structure of mycobionts and photobionts of the widespread lichen Cetraria aculeata
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2011.05168.xopenalex-snapshot
Do photobionts influence the ecology of lichens? A case study of environmental preferences in symbiotic green alga Asterochloris (Trebouxiophyceae)
inferred← citeshttps://doi.org/10.1111/j.1462-2920.2010.02386.xopenalex-snapshot
Two Trebouxia algae with different physiological performances are ever‐present in lichen thalli of Ramalina farinacea . Coexistence versus Competition?
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2007.02241.xopenalex-snapshot
Dissociation and horizontal transmission of codispersing lichen symbionts in the genus Lepraria (Lecanorales: Stereocaulaceae)
inferred← citeshttps://doi.org/10.1111/j.1529-8817.2008.00556.xopenalex-snapshot
PHYLOGENETIC PATTERNS AMONG NOSTOC CYANOBIONTS WITHIN BI‐ AND TRIPARTITE LICHENS OF THE GENUS PANNARIA1
inferred← citeshttps://doi.org/10.1111/j.1529-8817.2011.00962.xopenalex-snapshot
PHYLOGENETIC DIVERSITY OF TRENTEPOHLIALEAN ALGAE ASSOCIATED WITH LICHEN-FORMING FUNGI1
inferred← citeshttps://doi.org/10.1111/j.1574-6941.2010.01002.xopenalex-snapshot
Photobiont association and genetic diversity of the optionally lichenized fungus Schizoxylon albescens
inferred← citeshttps://doi.org/10.1111/j.1574-6941.2012.01422.xopenalex-snapshot
Lichen myco- and photobiont diversity and their relationships at the edge of life (McMurdo Dry Valleys, Antarctica)
inferred← citeshttps://doi.org/10.1111/jbi.12697openalex-snapshot
Comparison of phylogeographical structures of a lichen‐forming fungus and its green algal photobiont in western North America
inferred← citeshttps://doi.org/10.1111/jeu.12159openalex-snapshot
Algal and Fungal Diversity in Antarctic Lichens
inferred← citeshttps://doi.org/10.1111/jpy.12446openalex-snapshot
Heveochlorella (Trebouxiophyceae): a little‐known genus of unicellular green algae outside the Trebouxiales emerges unexpectedly as a major clade of lichen photobionts in foliicolous communities
inferred← citeshttps://doi.org/10.1111/mec.13271openalex-snapshot
Fungal specificity and selectivity for algae play a major role in determining lichen partnerships across diverse ecogeographic regions in the lichen‐forming family Parmeliaceae (Ascomycota)
inferred← citeshttps://doi.org/10.1111/mec.14764openalex-snapshot
The complexity of symbiotic interactions influences the ecological amplitude of the host: A case study in Stereocaulon (lichenized Ascomycota)
inferred← citeshttps://doi.org/10.1111/mec.15700openalex-snapshot
Extensive photobiont sharing in a rapidly radiating cyanolichen clade
inferred← citeshttps://doi.org/10.1111/nph.12678openalex-snapshot
Molecular phylogeny and symbiotic selectivity of the green algal genus Dictyochloropsis s.l. (Trebouxiophyceae): a polyphyletic and widespread group forming photobiont‐mediated guilds in the lichen family Lobariaceae
inferred← citeshttps://doi.org/10.1134/s1062359016040038openalex-snapshot
Lichen symbiosis: Search and recognition of partners
inferred← citeshttps://doi.org/10.1186/s12866-015-0527-0openalex-snapshot
Distribution patterns of haplotypes for symbionts from Umbilicaria esculenta and U. muehlenbergii reflect the importance of reproductive strategy in shaping population genetic structure
inferred← citeshttps://doi.org/10.13158/heia.29.2.2016.383openalex-snapshot
Phylogenetic Data and Chemical Traits Characterize a New Species in the Lichen Genus Tephromela
inferred← citeshttps://doi.org/10.1371/journal.pone.0089876openalex-snapshot
Do Photobiont Switch and Cephalodia Emancipation Act as Evolutionary Drivers in the Lichen Symbiosis? A Case Study in the Pannariaceae (Peltigerales)
inferred← citeshttps://doi.org/10.15407/978-966-00-1954-6openalex-snapshot
Prodromus of Spore Plants of Ukraine: Algae. Book 2.
inferred← citeshttps://doi.org/10.1639/0007-2745(2007)110[146:rlol]2.0.co;2openalex-snapshot
Recent literature on lichens—204
inferred← citeshttps://doi.org/10.1639/0007-2745-112.2.404openalex-snapshot
Symbiont flexibility in Thamnolia vermicularis (Pertusariales: Icmadophilaceae)
inferred← citeshttps://doi.org/10.1639/0007-2745-115.2.243openalex-snapshot
Further photomorphs in the lichen family Lobariaceae from Reunion (Mascarene archipelago) with notes on the phylogeny of Dendriscocaulon cyanomorphs
inferred← citeshttps://doi.org/10.1639/0007-2745-116.2.149openalex-snapshot
Symbiont flexibility in subalpine rock shield lichen communities in the Southwestern USA
inferred← citeshttps://doi.org/10.2139/ssrn.7244696openalex-snapshot
An integrated approach to unmasking the plastisphere-associated deterioration of modern heritage: Preserving the memory of the iconic red Kiosk K67
inferred← citeshttps://doi.org/10.2216/17-134.1openalex-snapshot
The hidden diversity of lichenised Trebouxiophyceae (Chlorophyta)
inferred← citeshttps://doi.org/10.3389/fmicb.2020.00268openalex-snapshot
Microbiome in Cladonia squamosa Is Vertically Stratified According to Microclimatic Conditions
inferred← citeshttps://doi.org/10.3389/fmicb.2021.774839openalex-snapshot
Turnover of Lecanoroid Mycobionts and Their Trebouxia Photobionts Along an Elevation Gradient in Bolivia Highlights the Role of Environment in Structuring the Lichen Symbiosis
inferred← citeshttps://doi.org/10.3389/fmicb.2022.779784openalex-snapshot
Phylogeny and Ecology of Trebouxia Photobionts From Bolivian Lichens
inferred← citeshttps://doi.org/10.3390/encyclopedia2030096openalex-snapshot
Lichen as Multipartner Symbiotic Relationships
inferred← citeshttps://doi.org/10.3390/plants1020039openalex-snapshot
Photobiont Relationships and Phylogenetic History of Dermatocarpon luridum var. luridum and Related Dermatocarpon Species
inferred← citeshttps://doi.org/10.3897/mycokeys.61.38175openalex-snapshot
Morphology and secondary chemistry in species recognition of Parmelia omphalodes group – evidence from molecular data with notes on the ecological niche modelling and genetic variability of photobionts
inferred← citeshttps://doi.org/10.3897/mycokeys.96.98029openalex-snapshot
Pseudolepraria, a new leprose genus revealed in Ramalinaceae (Ascomycota, Lecanoromycetes, Lecanorales) to accommodate Lepraria stephaniana
inferred← citeshttps://doi.org/10.5586/asbp.89311openalex-snapshot
One Name – One Fungus: The Influence of Photosynthetic Partners on the Taxonomy and Systematics of Lichenized Fungi
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