The phylogeny of Lecidella species is studied, based on a 7-locus data set using ML and Bayesian analyses. Phylogenetic relationships among 43 individuals representing 11 Lecidella species, mainly from mainland China, were included in the analyses and phenotypical characters studied and mapped onto the phylogeny. The Lecidella species fall into three major clades, which are proposed here as three informal groups–Lecidella stigmatea group, L. elaeochroma group and L. enteroleucella group, each of them strongly supported. Our phylogenetic analyses support traditional species delimitation based on morphological and chemical traits in most but not all cases. Individuals considered as belonging to the same species based on phenotypic characters were found to be paraphyletic, indicating that cryptic species might be hidden under these names (e.g. L. carpathica and L. effugiens). Potentially undescribed species were found within the phenotypically circumscribed species L. elaeochroma and L. stigmatea. Additional sampling across a broader taxonomic and geographic scale will be crucial to fully resolving the taxonomy in this cosmopolitan genus.
Citation: Zhao X, Zhang LL, Zhao ZT, Wang WC, Leavitt SD, Lumbsch HT (2015) A Molecular Phylogeny of the Lichen Genus Lecidella Focusing on Species from Mainland China. PLoS ONE 10(9): e0139405. https://doi.org/10.1371/journal.pone.0139405
Editor: Nico Cellinese, University of Florida, UNITED STATES
Received: July 20, 2015; Accepted: September 11, 2015; Published: September 28, 2015
Copyright: © 2015 Zhao et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data including Genbank and TreeBase numbers are within the paper and its Supporting Information files.
Funding: This work was supported by the China Scholorship Council (www.csc.edu.cn) 201408370093 to XZ, National Natural Science Foundation of China (www.nsfc.gov.cn) 31170187 to ZTZ and the National Natural Science Foundation of China (www.nsfc.gov.cn) 31270059 to LLZ. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
The circumscription of lichen-forming fungal species has traditionally been guided by morphological, chemical and ecological features. However, because lichens generally display few taxonomically useful characters, of which many are widely variable and the homology of character states within and among groups is difficult to assess [1–4]. Therefore, molecular data have gained importance in lichen systematics and now have a significant impact on the classification and taxonomy of lichenized ascomycetes [5–9]. Many phylogenetic studies of lichenized ascomycetes are designed to test morphology-based classifications. As a result, the systematic value of morphological characters in diverse groups of lichen-forming fungi is now much better understood [10–15]. Recent studies indicate that while phenotypical characters are useful in discriminating distinct lineages in many cases, they may fail to separate distinct species-level lineages with similar morphologies and/or chemistries [16–21]. In some cases, cryptic lineages correspond to geographically isolated areas, often continents, and are well documented in foliose or fruticose lichens. However, less is known about the presence and biogeography of cryptic lineages in crustose lichens.
The genus Lecidella Körb. (Lecanoraceae; ) is a medium-size genus with approximately 80 accepted species . The species are distinguished based on a few taxonomically diagnostic morphological and anatomical characters, in addition to secondary chemistry. The genus is generally regarded as taxonomically difficult due to a high degree of variation and/or plasticity in diagnostic characters. As lecideoid lichens, Lecidella was considered to be part of the huge genus Lecidea Ach. for a long time . Although Lecidella was established by Körber in 1855 , the genus was not widely used until Hertel  recognized it as a subgenus of Lecidea and subsequently  at generic level mainly based on the secondary chemistry which differs from Lecidea in the presence of chlorinated norlichexanthones. Lecidella was classified in Lecanoraceae [28, 29] mainly based on the similarity in ascus-type. Our knowledge of species delimitation in the genus vastly improved over the last decades with the improvement of identification of chlorinated xanthones using TLC (thin layer chromatography), HPLC (high performance liquid chromatography), and mass spectrometry [30–39]. As currently circumscribed, Lecidella is comprised of crustose lichens characterized by black lecideine apothecia, persistent proper excipulum, clavate, large amyloid, eight-spored asci referred to as Lecidella-type , paraphyses that typically separate readily in KOH, simple, hyaline, non-halonate ascospores, curved, filiform conidia and the occurrence of xanthones in the majority of species. The genus is widespread, from the tropics to polar regions, occurring on various substrata, including rock, detritus, bark, wood and mosses. Presently, about 10 species of Lecidella have been reported in mainland China [40–42].
Currently our knowledge of the phylogeny of Lecidella is limited, with only a few studies including representatives from this genus [43–49]. While these few studies support the monophyly of Lecidella and its placement in Lecanoraceae, none have included a broader taxonomic sampling to address the evolutionary relationships of species within the genus. Here we address the phylogeny of the genus using a concatenated data set of seven loci (two loci from the nuclear ribosomal cistron, one mitochondrial ribosomal, and four nuclear protein-coding genes) for selected taxa of Lecidella, with a focus on species from mainland China. The main goals of this study were 1) to evaluate the current delimitation of selected morphospecies within Lecidella and 2) to reconstruct phylogenetic relationships among species of this genus.
Materials and Methods
MorphologicAl and chemical studies
Approximately 1000 specimens of Lecidella collected in mainland China were studied primarily from the herbarium: SDNU, and also the herbaria: DUKE, F, HMAS-L, and KUN-L. The field studies did not involve endangered or protected species, and no specific permissions were required to collect specimens from these localities. Specimens were examined using standard microscopy techniques and hand-cut sections under a dissecting microscope (Nikon SMZ 745T), anatomical characters were observed under a compound microscope in water (OLYMPUS CX21). Secondary metabolites were identified using thin-layer chromatography with solvent C (toluene: acetic acid = 170:30) [50, 51]. Specimens representing the range of morphological and chemical variation were selected for molecular phylogenetic investigations.
Taxon sampling and molecular data
For our phylogenetic analyses, we selected a total of 51 Lecidella specimens collected from different regions of mainland China. These specimens represented 11 currently recognized species–L. carpathica, L. effugiens, L. elaeochroma, L. aff. elaeochroma, L. elaeochromoides, L. enteroleucella, L. euphorea, L. aff. euphorea, L. patavina, L. stigmatea and L. tumidula (S1 Table). Each species was represented by at least two specimens. Molecular data were generated for seven loci: the internal transcribed spacer (ITS), nuclear large subunit (nucLSU), mitochondrial small subunit (mtSSU), minichromosome maintenance complex component 7 (MCM7), ribosome biogenesis gene (TSR1), the largest subunit of the RNA polymerase II gene (RPB1) and the second largest subunit of RNA polymerase II gene (RPB2). Sequences generated for this study were complemented with sequences from GenBank representing additional specimens or species: L. elaeochroma, L. euphorea, L. flavosorediate, L. greenii, L. meiococca, L. siplei, L. stigmatea and L. wulfenii (S2 Table). Rhizoplaca parilis, R. porterii, Protoparmeliopsis achariana and P. muralis were selected as outgroups (S2 Table).
To obtain fungal sequences apothecia were used for extracting total genomic DNA using the Prepease DNA Isolation Kit (USB, Cleveland, OH, USA), following the leaf extraction protocol. Ready-To-Go PCR Beads were used (GE Healthcare) for the amplification of the targeted loci. A new forward primer for amplifying the RPB2 locus of Lecidella was designed for this study, and all primers and PCR settings [52–63] are summarized in Table 1. PCR products were purified using Exo SAP-IT (USB, Cleveland, OH, USA), following the manufacturers’ instructions. Sequencing reactions were performed using BigDye Terminator v3.1 (Applied Biosystems, Foster City, CA,USA) and using the same primers as those used for amplification. Sequenced products were then run on an ABI 3730 automated sequencer according to established protocols (Applied Biosystems) at the Pritzker Laboratory for Molecular Systematics at the Field Museum, Chicago, IL, USA.
Contigs were assembled and edited using the program Geneious v6.1.2 (Biomatters Ltd., Auckland, NZ). Sequences of each locus were aligned using the program MAFFT v7 . For ITS sequences, we used the L-ING-i alignment algorithm with the remaining parameters set to default values. For nucLSU, G-ING-i algorithm and “leave gappy regions” were selected. Then we used E-ING-i algorithm for mtSSU and RPB1, and G-ING-i algorithm for MCM7, TSR1 and RPB2, with the remaining parameters set to default values. Ambiguous positions of the ITS and mtSSU alignments were removed using Gblocks  implementing all the options for a less stringent selection. We compiled two data matrices: the ‘ITS matrix’ included ITS sequences of all of our samples (Table 2) and all taxa of Lecidella available from GenBank (S2 Table); and the ‘multilocus matrix’ was a concatenated dataset comprised of specimens that were represented by at least two of seven targeted loci (Table 2). A summary of alignment information for the multilocus dataset was provided (Table 3). The ‘multilocus matrix’ included a total of 47 individuals representing 16 taxa.
The numbers behind the specific epithet are used to distinguish different individuals for each species.
The single-locus alignments were concatenated in Geneious for the subsequent phylogenetic analyses. Maximum likelihood (ML) analyses were carried out on the ‘multilocus matrix’ using locus-specific model partitions (ITS, nucLSU, mtSSU, MCM7, RPB1, RPB2 and TSR1) in RAxML v8.1.11 . We were unable to generated MCM7 and TSR1 sequences from the majority of specimens, and therefore we did another partitioned ML analyses limited to the five most thoroughly sampled loci (ITS, nucLSU, mtSSU, RPB1 and RPB2). A search combining 200 separate ML searches was conducted, implementing a GTRGAMMA model, and 1000 pseudoreplicates to evaluate bootstrap support for each node. A ML topology was also inferred from the ‘ITS matrix’ using RAxML and search parameters as described above. In addition to the ML analysis, the ‘multilocus matrix’ was also subjected to a Bayesian analysis with MrBayes v3.2.3 . The nucleotide substitution models of the seven loci were selected using the Akaike information criterion in jModelTest v2.1.7 . The Bayesian analysis was run for 10,000,000 generations with four independent chains and sampling every 1000th tree. All model parameters were unlinked. Two independent Bayesian runs were conducted to ensure that stationarity was reached and the runs converged at the same log-likelihood level (verified by eye and with AWTY option; ). After discarding the burn-in, the remaining 7500 trees of each run were pooled to calculate a 50% majority rule consensus tree. The clades that received bootstrap support ≥70% under ML and posterior probabilities ≥0.95 were considered significant. Phylogenetic trees were visualized using FigTree v1.4.2 .
For this study, 63 new sequences were generated (Table 2). The two datasets we used in this study were deposited in TreeBase (ID #17997). The ‘ITS matrix’ consisted of 60 individuals and 550 aligned nuclecotide position characters. The concatenated, ‘multilocus matrix’ consisted of 47 individuals and 4260 aligned nuclecotide position characters (Table 3). Phylogenies derived from the ML and B/MCMC analyses were generally concordant. ML analysis of the seven-locus and five-locus matrices also produced topologies that were generally concordant, and the seven-locus phylogeny is presented here, with nodal support values from both ML bootstrap analysis and posterior probabilities from the Bayesian inference (Fig 1). We listed 13 phenotypical characters next to the ML tree (Fig 1). The phylogenies resulting from the ML analyses of the ITS matrix and the five-locus matrix were shown in S1 and S2 Figs.
Branches in bold received maximum likelihood bootstrap support values equal or above 70% and posterior probabilities equal or above 0.95. Phenotypical characters listed in boxes right to the tree. 1. Color of epihymenium: 0 = olive-brown (sometimes with green tinge); 1 = violet-brown; 2 = green to dark-green. 2. Hymenium: 0 = not inspersed; 1 = slightly inspersed; 2 = inspersed. 3. Color of hypothecium: 0 = colorless; 1 = yellow-brown to red-brown. 4. Arthothelin: 0 = absent; 1 = present as minor substance; 2 = present as a major substance. 5. Thiophanic acid: 0 = absent; 1 = present. 6. Aotearone: 0 = absent; 1 = present. 7. Capistratone: 0 = absent; 1 = present as minor substance; 2 = present as major substance. 8. Thuringione: 0 = absent; 1 = present as minor substance; 2 = present as major substance. 9. Granulosin: 0 = absent; 1 = present. 10. Lichexanthone: 0 = absent; 1 = present. 11. Diploicin: 0 = absent; 1 = present. 12. Zeorin: 0 = absent; 1 = present. 13. Substratum: 0 = corticolous; 1 = lignicolous; 2 = saxicolous. (? indicates samples that were unavailable for study)
The most likely tree was comprised of three main, well-supported (bs = 100%, pp = 1.0) clades (Fig 1). Lecidella enteroleucella formed a highly supported clade (bs = 100%, pp = 1.0) sister to L. carpathica, L. effugiens, L. elaeochroma, L. aff. elaeochroma, L. elaeochromoides, L. euphorea, L. aff. euphorea, L. meiococca, and L. tumidula, which together formed a well-supported clade (bs = 100%, pp = 1.0). The species L. stigmatea and L. patavina formed a well-supported sister-group (bs = 100%, pp = 1.0) to the other two clades. All species with colorless hypothecium and lacking xanthones, which refer to L. stigmatea and L. patavina in the seven-gene tree (Fig 1) and L. greenii, L. siplei, L. stigmatea and L. patavina in the ITS tree (S1 Fig) formed a monophyletic lineage. Lecidella enteroleucella, which is characterized by a colorless hypothecium and contains the chlorinated xanthones thuringione and arthothelin, formed a separate clade. While most species which have yellow-brown to brown hypothecium and contain xanthones formed a separate clade, the traditionally circumscribed species L. carpathica was not recovered as a monophyletic lineage but clustered with L. tumidula in both trees.
Here we provide the first phylogenetic hypothesis for the cosmopolitan lichen-forming fungal genus Lecidella. In most cases, our phylogenetic analyses support the traditional species delimitation based on morphological and chemical traits. The phylogeny also indicated that the species diversity of Lecidella in China is higher than previously assumed. The role of secondary metabolites in species delimitation of the genus Lecidella is supported. Below we discuss each of the three major Lecidella clades recovered in this study.
Lecidella stigmatea clade
This clade includes L. stigmatea and L. patavina and is characterized by a colorless hypothecium and secondary compounds other than xanthones. The two species were distinguished previously on a combination of characters, the inspersion of the hymenium being the most important . Our phylogeny does not support the hymenial inspersion as being a major trait to characterize clades in the group. All L. stigmatea specimens collected in China have an olive-brown to brown (sometimes with green tinge) epihymenium regardless of the age of apothecia, while the samples identified as L. patavina have a green to dark-green epihymenium. In the ITS phylogeny (S1 Fig), L. patavina and L. stigmatea do not form monophyletic groups either and this indicates that the species circumscription in this group needs re-evaluation. Also, L. greenii is nested within the clade but forms a strongly supported monophyletic group. In the ITS tree (S1 Fig) the specimen ‘L. patavina2’ clusters with the Antarctic species L. siplei sensu Inoue [48, 71] and is also morphologically similar. With the data at hand we cannot conclude whether cryptic species are present in this group or whether the species are morphologically and chemically variable. However, the presence of well-supported groups within the clade suggests that cryptic species might be hidden under the names L. patavina and L. stigmatea. Our taxon sampling is insufficient to address this issue. The lignicolous sample ‘L. stigmatea4’ differs from the other L. stigmatea specimens in having a violet-brown epihymenium and thinner proper excipulum but otherwise agrees well morphologically with the saxicolous specimens of that species. In the ITS tree (S1 Fig) it is also separate from the other samples in this clade. Additional material will be necessary to determine whether it represents an undescribed taxon.
Lecidella elaeochroma clade
This clade forms a well-supported monophyletic group in the phylogenies inferred from the ‘multilocus matrix’ (bs = 100%, pp = 1.0) and ‘ITS matrix’ (bs = 100%) and contains L. carpathica, L. effugiens, L. elaeochroma, L. aff. elaeochroma, L. elaeochromoides, L. euphorea, L. aff. euphorea, L. meiococca, and L. tumidula. In the ITS topology, L. wulfenii and L. flavosorediata were also recovered within this clade. All species within this clade are known to produce xanthones. According to Leuckert and Knoph  the xanthones in Lecidella mainly consist of two types: chloronorlichexanthones (arthothelin and thiophanic acid in our samples) and O-methylated xanthones (aotearone, capistratone, thuringione, granulosin and lichexanthone in our samples). Our results indicate that both major groups of xanthones are not completely independent from one another, being present for example in L. euphorea, which contains arthothelin and thiophanic acid but also aotearone and capistratone. Lecidella euphorea and L. tumidula form well-supported monophyletic clades. Lecidella tumidula3 was originally identified as L. euphorea . However, a re-examination of the voucher specimen from DUKE revealed the presence of lichexanthone in this specimen; hence it was re-identified as L. tumidula. Lecidella carpathica is paraphyletic with L. tumidula nested within. In the ITS tree (S1 Fig), specimens Lecidella ‘carpathica1’ and ‘carpathica2’ cluster with a sequence from Genbank that was collected in Austria and apparently represents L. carpathica s.str., whereas specimens ‘carpathica0’ and ‘carpathica3’ form a sister-group to L. tumidula and potentially represent a cryptic lineage.
In our tree, L. elaeochroma is polyphyletic. A specimen from Xinjiang in NW China named L. ‘elaeochroma3’ did not cluster with L. ‘elaeochroma5’, which was collected in Europe (Belgium). The latter clustered in the ITS tree with numerous other sequences of L. elaeochroma and probably represents L. elaeochroma s. str., whereas the Chinese sample appear to represent an undescribed species. In addition, three samples were identified as Lecidella aff. elaeochroma here. They were collected in NE China (Jilin province) and have a brownish epihymenium (vs. greenish), a heavily inspersed hymenium (vs. non- to slightly inspersed), and a violet pigment in the excipulum. The samples also formed a separate, strongly supported monophyletic clade and might represent a new species (Fig 1). Lecidella elaeochromoides and L. effugiens, which were traditionally separated based on a combination of somewhat overlapping thalline and apothecial characters, and differences in chemical composition [33, 34], were not supported as distinct clades, suggesting these taxa may be conspecific. However, L. effugiens is not monophyletic and itself consist of two clades with two specimens (‘effugiens2’ and ‘effugiens3’) collected in NE and SW China potentially representing a cryptic lineage that is sister to L. aff. euphorea (Fig 1). The latter is only distantly related to L. euphorea but is morphologically similar. It, however, differs in its secondary chemistry, containing aotearone but lacking capistratone or lacking xanthones altogether (specimen 5).
Lecidella enteroleucella clade
Lecidella enteroleucella individually forms a monophyletic group. The small apothecia (less than 0.4mm in diam.) are unique in the genus. The species agrees with the L. elaeochroma clade in containing chlorinated xanthones. In our tree the species forms a sister-group to that clade and no close relatives are known. However, L. oceanica, which was reported from Korea  and China , is morphologically similar but has a different chemistry (containing capistratone as major substance). We failed to generate DNA sequences of this species but hypothesize that L. oceanica also falls within this clade.
The current study provides important insight into the evolution and classification of Lecidella. Combining morphology, chemistry and phylogeny, the three informal groups within Lecidella–L. elaeochroma group, L. enteroleucella group and L. stigmatea group are proposed in this study. Additional sampling across a broader taxonomic and geographic scale will be crucial to fully resolving taxonomy in this cosmopolitan lineage.
S1 Fig. Maximum Likelihood topology of Lecidella inferred from ITS sequences.
ML bootstrap frequencies are shown above branches.
S2 Fig. Maximum Likelihood topology of Lecidella inferred from the five-locus matrix.
ML bootstrap frequencies are shown above branches.
S1 Table. The detailed collection information for the Lecidella specimens selected for this study.
We are thankful to Ms. Deng Hong (HMAS-L) and Mr. Wang Li Song (KUN-L) for providing access to specimens deposited in their herbaria, and grateful to M. McMullen (Duke Univ. Herbarium) for sending us Lecidella specimens for examination on loan.
Conceived and designed the experiments: XZ LLZ HTL. Performed the experiments: XZ SDL. Analyzed the data: XZ HTL. Contributed reagents/materials/analysis tools: XZ SDL HTL. Wrote the paper: XZ LLZ ZTZ WCW SDL HTL.
- 1. Rivas Plata E, Lumbsch HT. Parallel evolution and phenotypic divergence in lichenized fungi: a case study in the lichen-forming fungal family Graphidaceae (Ascomycota: Lecanoromycetes: Ostropales). Molecular Phylogenetics and Evolution. 2011;61(1):45–63. pmid:MEDLINE:21605691.
- 2. Grube M, Baloch E, Lumbsch HT. The phylogeny of Porinaceae (Ostropomycetidae) suggests a neotenic origin of perithecia in Lecanoromycetes. Mycological Research. 2004;108:1111–8. pmid:ISI:000224794900001.
- 3. Schmitt I, del Prado R, Grube M, Lumbsch HT. Repeated evolution of closed fruiting bodies is linked to ascoma development in the largest group of lichenized fungi (Lecanoromycetes, Ascomycota). Molecular Phylogenetics and Evolution. 2009;52(1):34–44. pmid:ISI:000266692800004.
- 4. Tehler A, Irestedt M. Parallel evolution of lichen growth forms in the family Roccellaceae (Arthoniales, Ascomycota). Cladistics. 2007;23:432–54. pmid:ISI:000249881100002.
- 5. Lumbsch HT. Phylogeny of filamentous ascomycetes. Naturwissenschaften. 2000;87(8):335–42. pmid:ISI:000089214200001.
- 6. Lumbsch HT. Recent trends in phylogeny and classification of lichen-forming ascomycetes. In: Ganguli BN, Deshmukh SK, editors. Fungi Multifaceted Microbes: Anamaya Publishers, New Delhi. 321 pp.; 2006. p. 153–68.
- 7. Grube M, Winka K. Progress in understanding the evolution and classification of lichenized ascomycetes. Mycologist. 2002;16:67–76. pmid:26257.
- 8. DePriest PT. Early molecular investigations of lichen-forming symbionts: 1986–2001. Annual Review of Microbiology. 2004;58:273–301. pmid:27086.
- 9. Printzen C. Lichen Systematics: The Role of Morphological and Molecular Data to Reconstruct Phylogenetic Relationships. In: Lüttge U, Beyschlag W, Büdel B, Francis D, editors. Progress in Botany 712010. p. 233–75.
- 10. Jaklitsch WM, Baral HO, Lücking R, Lumbsch HT. Ascomycota. In: Frey W, editor. Syllabus of Plant Families—Adolf Engler’s Syllabus der Pflanzenfamilien. 1/2. 13 ed. Stuttgart: Gebr. Borntraeger Verlagsbuchhandlung; 2015. p. 150.
- 11. Otálora MA, Aragón G, Martínez I, Wedin M. Cardinal characters on a slippery slope—A re-evaluation of phylogeny, character evolution, and evolutionary rates in the jelly lichens (Collemataceae s. str). Molecular and Phylogenetic Evolution. 2013;68:185–98. pmid:34539.
- 12. Divakar PK, Kauff F, Crespo A, Leavitt SD, Lumbsch HT. Understanding phenotypical character evolution in parmelioid lichenized fungi (Parmeliaceae, Ascomycota). PLoS ONE. 2013;8(11):e83115. pmid:MEDLINE:24312438.
- 13. Wedin M, Wiklund E, Jørgensen PM, Ekman S. Slippery when wet: phylogeny and character evolution in the gelatinous cyanobacterial lichens (Peltigerales, Ascomycetes). Molecular Phylogenetics and Evolution. 2009;53:862–71. pmid:31603.
- 14. Gueidan C, Roux C, Lutzoni F. Using a multigene phylogenetic analysis to assess generic delineation and character evolution in Verrucariaceae (Verrucariales, Ascomycota). Mycological Research. 2007;111:1145–68. pmid:WOS:000251860500001.
- 15. Lumbsch HT, Parnmen S, Kraichak E, Papong K, Lücking R. High frequency of character transformations is phylogenetically structured within the lichenized fungal family Graphidaceae (Ascomycota: Ostropales). Systematics and Biodiversity. 2014;12(3):271–91.
- 16. Lücking R, Dal-Forno M, Sikaroodi M, Gillevet PM, Bungartz F, Moncada B, et al. A single macrolichen constitutes hundreds of unrecognized species. Proceedings of the National Academy of Sciences of the United States of America. 2014;111(30):11091–6. pmid:WOS:000339500200054.
- 17. Amo de Paz G, Crespo A, Cubas P, Elix JA, Lumbsch HT. Transoceanic dispersal and subsequent diversification on separate continents shaped diversity of the Xanthoparmelia pulla group (Ascomycota). PLoS ONE. 2012;7(6):e39683. pmid:22745810
- 18. Otálora MAG, Martínez I, Aragón G, Molina MC. Phylogeography and divergence date estimates of a lichen species complex with a disjunct distribution pattern. American Journal of Botany. 2010;97:216–23. pmid:32109.
- 19. Elix JA, Corush J, Lumbsch HT. Triterpene chemosyndromes and subtle morphological characters characterise lineages in the Physcia aipolia group in Australia (Ascomycota). Systematics and Biodiversity. 2009;7(4):479–87. pmid:ISI:000272723500012.
- 20. Parnmen S, Rangsiruji A, Mongkolsuk P, Boonpragob K, Nutakki A, Lumbsch HT. Using phylogenetic and coalescent methods to understand the species diversity in the Cladia aggregata complex (Ascomycota, Lecanorales). PLoS ONE. 2012;7(12)(12):e52245. pmid:WOS:000312483300072.
- 21. Arguello A, Del Prado R, Cubas P, Crespo A. Parmelina quercina (Parmeliaceae, Lecanorales) includes four phylogenetically supported morphospecies. Biological Journal of the Linnean Society. 2007;91(3):455–67. pmid:ISI:000247817100011.
- 22. Lumbsch HT, Huhndorf SM. Myconet Volume 14. Part One. Outline of Ascomycota—2009. Fieldiana (Life and Earth Sciences). 2010;1:1–42.
- 23. Kirk PM, Cannon PF, Minter DW, Stalpers JA, editors. Ainsworth & Bisby's Dictionary of the Fungi. 10th ed. Wallingford: CAB International; 2008.
- 24. Hertel H. Über saxicole, lecideoide Flechten der Subantarktis. Beiheft zur Nova Hedwigia. 1984;79:399–499. pmid:8459.
- 25. Koerber GW. Systema Lichenum Germaniae (I-XXXIV). Die Flechten Deutschlands mikroscopisch geprüft, kritisch gesichtet, charakteristisch beschrieben und systematisch geordnet: Breslau; 1855.
- 26. Hertel H. Revision einiger calciphiler Formenkreise der Flechtengattung Lecidea. Beihefte zur Nova Hedwigia. 1967;24:1–155. pmid:8414.
- 27. Leuckert C, Hertel H. Über Flechtenstoffe und Systematik einiger Arten der Gattung Lecidea. Nova Hedwigia. 1967;14:291–300. pmid:11406.
- 28. Hafellner J. Durch Ascusstrukturanalysen zun einem besseren Verständnis der Systematik der Lecideaceae coll. (lichenisierte Ascomycetes). Mitteilungsband Botaniker-Tagung Wien1984. p. 116.
- 29. Hafellner J. Studien in Richtung einer natürlicheren Gliederung der Sammelfamilien Lecanoraceae und Lecideaceae. Beiheft zur Nova Hedwigia. 1984;79:241–371. pmid:7251.
- 30. Elix JA, Crook CE. The joint occurrence of chloroxanthones in lichens, and a further thirteen new lichen xanthones. Bryologist. 1992;95:52–64. pmid:4875.
- 31. Knoph J-G. Untersuchungen an gesteinsbewohnenden xanthonhaltigen Sippen der Flechtengattung Lecidella (Lecanoraceae, Lecanorales) unter besonderer Berücksichtigung von aussereuropäischen Proben exklusive Amerika. Bibliotheca Lichenologica. 1990;36:1–183. pmid:10253.
- 32. Leuckert C, Knoph J-G, Ziegler HG, Hertel H. Chemotaxonomische Studien in der Gattung Lecidella (Lecanorales, Lecanoraceae) I. Herzogia. 1990;8:265–72. pmid:11413.
- 33. Leuckert C, Knoph J-G. European taxa of saxicolous Lecidella containing chloroxanthones: identification of patterns using thin layer chromatography. Lichenologist. 1992;24:383–97. pmid:11411.
- 34. Leuckert C, Knoph J-G, Hertel H. Chemotaxonomische Studien in der Gattung Lecidella (Lecanorales, Lecanoraceae) II. Europäische Arten der Lecidella asema-Gruppe. Herzogia. 1992;9:1–17. pmid:11410.
- 35. Leuckert C, Knoph J-G. Secondary compounds as taxonomic characters in the genus Lecidella (Lecanoraceae, Lecanorales). Bibliotheca Lichenologica. 1993;53:161–71. pmid:11412.
- 36. Knoph J-G, Leuckert C. Chemotaxonomic studies in the saxicolous species of the lichen genus Lecidella (Lecanorales, Lecanoraceae) in America. Nova Hedwigia. 1994;59:455–508. pmid:10252.
- 37. Knoph J-G, Leuckert C, Hertel H. Chemotypes and distribution patterns of saxicolous species of Lecidella (Lecanoraceae, Lecanorales). Cryptogamic Botany. 1995;5:45–54. pmid:10251.
- 38. Knoph J-G, Leuckert C. Chemotypes and distribution patterns of the non-saxicolous species of Lecidella (Lecanoraceae, Lecanorales). Bibliotheca Lichenologica. 1997;68:129–34. pmid:10242.
- 39. Knoph J-G, Leuckert C. Chemotaxonomische Studien in der Gattung Lecidella (Lecanorales, Lecanoraceae) III. Die gesteinsbewohnenden Arten mit farblosem Hypothecium unter besonderer Berücksichtigung von europäischem Material. Herzogia. 2000;14:1–26. pmid:21139.
- 40. Wei JC. An Enumeration of Lichens in China. Beijing: International Academic Publishers; 1991.
- 41. Abbas A, Mijit H, Tumur A, Jinong W. A checklist of the lichens of Xinjiang, China. Harvard Papers in Botany. 2001;5(2):359–70.
- 42. Zhang L-L, Wang L-S, Wang H-Y, Zhao Z-T. Four new records of lecideoid lichens from China. Mycotaxon. 2012;119:445–51. pmid:33842.
- 43. Ekman S, Wedin M. The phylogeny of the families Lecanoraceae and Bacidiaceae (Lichenized Ascomycota) inferred from nuclear SSU rDNA sequences. Plant Biology. 2000;2(3):350–60. pmid:ISI:000087865600014.
- 44. Grube M, Baloch E, Arup U. A phylogenetic study of the Lecanora rupicola group (Lecanoraceae, Ascomycota). Mycological Research. 2004;108:506–14. pmid:ISI:000221995600006.
- 45. Miadlikowska J, Kauff F, Hofstetter V, Fraker E, Grube M, Hafellner J, et al. New insights into classification and evolution of the Lecanoromycetes (Pezizomycotina, Ascomycota) from phylogenetic analyses of three ribosomal RNA- and two protein-coding genes. Mycologia. 2006;98(6):1088–103. pmid:ISI:000245858800024.
- 46. Miadlikowska J, Kauff F, Högnabba F, Oliver JC, Molnár K, Fraker E, et al. Multigene phylogenetic synthesis for 1307 fungi representing 1139 infrageneric taxa, 312 genera and 66 families of the class Lecanoromycetes (Ascomycota). Molecular Phylogenetics and Evolution. 2014;79:132–68. pmid:24747130
- 47. Kalb K, Staiget B, Elix JA, Lange U, Lumbsch HT. A new circumscription of the genus Ramboldia (Lecanoraceae, Ascomycota) based on morphological and molecular evidence. Nova Hedwigia. 2008;86(1–2):23–42. pmid:ISI:000253880600002.
- 48. Ruprecht U, Lumbsch HT, Brunauer G, Green TGA, Turk R. Insights into the Diversity of Lecanoraceae (Lecanorales, Ascomycota) in continental Antarctica (Ross Sea region). Nova Hedwigia. 2012;94(3–4):287–306. pmid:WOS:000304431800002.
- 49. Zhao X, Leavitt SD, Zhao ZT, Zhang LL, Arup U, Grube M, et al. Towards a revised generic classification of lecanoroid lichens (Lecanoraceae, Ascomycota) based on molecular, morphological and chemical evidence. Fungal Diversity. 2015;xx:in prep.
- 50. Orange A, James PW, White FJ. Microchemical methods for the identification of lichens. London: British Lichen Society; 2001. 101 p.
- 51. Lumbsch HT. Analysis of phenolic products in lichens for identification and taxonomy. In: Kranner I, Beckett R, Varma A, editors. Protocols in Lichenology Culturing, biochemistry, ecophysiology and use in biomonitoring. Berlin: Springer; 2002. p. 281–95.
- 52. Gardes M, Bruns TD. ITS primers with enhanced specificity for basidiomycetes—Application to the identification of mycorrhizae and rusts. Molecular Ecology. 1993;2:113–8. pmid:8180733
- 53. Larena I, Salazar O, González V, Julián MC, Rubio V. Design of a primer for ribosomal DNA internal transcribed spacer with enhanced specificity for ascomycetes. Journal of Biotechnology. 1999;75:187–94. pmid:10553657
- 54. Döring H, Clerc P, Grube M, Wedin M. Mycobiont-specific PCR primers for the amplification of nuclear ITS and LSU rDNA from lichenized ascomycetes. Lichenologist. 2000;32:200–4. pmid:3972.
- 55. Mangold A, Martin MP, Lücking R, Lumbsch HT. Molecular phylogeny suggests synonymy of Thelotremataceae within Graphidaceae (Ascomycota: Ostropales). Taxon. 2008;57(2):476–86. pmid:ISI:000256687600009.
- 56. Vilgalys R, Hester M. Rapid genetic identification and mapping of enzymatically amplified ribosomal DNA from several Cryptococcus species. Journal of Bacteriology. 1990;172:4238–46. pmid:2376561
- 57. Zoller S, Scheidegger C, Sperisen C. PCR primers for the amplification of mitochondrial small subunit ribosomal DNA of lichen-forming ascomycetes. Lichenologist. 1999;31:511–6. pmid:ISI:000083572400011.
- 58. Zhou S, Stanosz GR. Primers for amplification of mtSSU rDNA, and a phylogenetic study of Botryosphaeria and associated anamorphic fungi. Mycological Research. 2001;105:1033–44.
- 59. Leavitt SD, Johnson L, St Clair LL. Species delimitation and evolution in morphologically and chemically diverse communities of the lichen-forming genus Xanthoparmelia (Parmeliaceae, Ascomycota) in western North America. American Journal of Botany. 2011;98(2):175–88. pmid:ISI:000286884500012.
- 60. Schmitt I, Crespo A, Divakar PK, Fankhauser J, Herman-Sackett E, Nelsen MP, et al. New primers for single-copy protein-coding genes for fungal systematics. Persoonia—Molecular Phylogeny and Evolution of Fungi. 2009;23:35–40.
- 61. Stiller JW, Hall BD. The origin of red algae: implications for plastid evolution. Proceedings of the National Academy of Sciences of the United States of America. 1997;94:4520–5. pmid:9114022
- 62. Matheny PB, Liu YJ, Ammirati JF, Hall BD. Using RPB1 and RPB2 nucleotide sequences (Inocybe; Agaricales). American Journal of Botany. 2002;89:688–98. pmid:21665669
- 63. Liu YJ, Whelen S, Hall BD. Phylogenetic relationships among ascomycetes: evidence from an RNA polymerase II subunit. Molecular Biology and Evolution. 1999;16:1799–808. pmid:10605121
- 64. Katoh K, Asimenos G, Toh H. Multiple Alignment of DNA Sequences with MAFFT. Methods in Molecular Biology. 2009;537:39–64. pmid:19378139
- 65. Castresana J. Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis. Molecular Biology and Evolution. 2000;17(4):540–52. pmid:ISI:000086337700008.
- 66. Stamatakis A. RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models. Bioinformatics. 2006;22:2688–90. pmid:16928733
- 67. Ronquist F, Teslenko M, van der Mark P, Ayres DL, Darling A, Höhna S, et al. MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Systematic Biology. 2012;61:539–42. pmid:22357727
- 68. Darriba D, Taboada GL, Doallo R, Posada D. jModelTest 2: more models, new heuristics and parallel computing. Nature Methods. 2012;9(8):772. pmid:22847109
- 69. Nylander JAA, Wilgenbusch JC, Warren DL, Swofford DL. AWTY (Are We There Yet?): a system for graphical exploration of MCMC convergence in Bayesian phylogenetics. Bioinformatics. 2008;24:581–3. pmid:17766271
- 70. Rambaut A. FigTree 1.2.2. http://tree.bio.ed.ac.uk/software/figtree/2009.
- 71. Inoue M. Lecideoid lichens of Prince Olav Coast and Sôya Coast, Enderby Land, East Antarctica. Nankyoku Shiryô. 1991;35:271–84. pmid:9134.
- 72. Schmull M, Miadlikowska J, Pelzer M, Stocker-Woergoetter E, Hofstetter V, Fraker E, et al. Phylogenetic affiliations of members of the heterogeneous lichen-forming fungi of the genus Lecidea sensu Zahlbruckner (Lecanoromycetes, Ascomycota). Mycologia. 2011;103(5):983–1003. pmid:WOS:000294529400006.
- 73. Zhang LL, Wang XY, Wang HY, Wang LS, Hur J-S. A new species and new records of saxicolous species of the genus Lecidella (Lecanoraceae) from South Korea. Bryologist. 2012;115(2):329–32. pmid:WOS:000307281700012.
- 74. Zhao X, Zhang LL, Sun LY, Hu L, Zhao ZT. Four new records of Lecanoraceae from China. Mycotaxon. 2015;in press.