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Catenarina (Teloschistaceae, Ascomycota), a new Southern Hemisphere genus with 7-chlorocatenarin

Published online by Cambridge University Press:  11 February 2014

Ulrik SØCHTING ,
Majbrit Zeuthen SØGAARD ,
John A. ELIX ,
Ulf ARUP ,
Arve ELVEBAKK  and
Leopoldo G. SANCHO
Ulrik SØCHTING
Affiliation:
Section for Ecology and Evolution, Department of Biology, University of Copenhagen, Universitetsparken 15, 2100 Copenhagen K, Denmark. Email: [email protected]
Majbrit Zeuthen SØGAARD
Affiliation:
Section for Ecology and Evolution, Department of Biology, University of Copenhagen, Universitetsparken 15, 2100 Copenhagen K, Denmark. Email: [email protected]
John A. ELIX
Affiliation:
Research School of Chemistry, Building 33, Canberra, A.C.T. 0200, Australia
Ulf ARUP
Affiliation:
Botanical Museum, Lund University, Box 117, SE-221 00 Lund, Sweden
Arve ELVEBAKK
Affiliation:
Tromsø University Museum, University of Tromsø, N-9037 Tromsø, Norway
Leopoldo G. SANCHO
Affiliation:
Universidad Complutense de Madrid, Departamento de Biología Vegetal II, Plaza de Ramón y Cajal s/n, S-28040 Madrid, Spain
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Abstract

A new genus, Catenarina (Teloschistaceae, Ascomycota), with three species is described from the Southern Hemisphere, supported by molecular data. All species contain the secondary metabolite 7-chlorocatenarin, previously unknown in lichens. Catenarinadesolata is a non-littoral, lichenicolous species found on volcanic and soft sedimentary rock at 190–300 m in and near steppes in southernmost Chile and on the subantarctic island, Kerguelen. Catenarina vivasiana grows on maritime rocks and on rock outcrops in lowland Nothofagus forests, but has also been found at altitudes up to c. 580 m on moss and detritus on outcrops in Tierra del Fuego. The Antarctic species Caloplaca iomma is transferred to Catenarina based on chemical data; it grows on rocks near the coast in maritime Antarctica.

Keywords

AntarcticaArgentinaCaloplacaChileHPLCKerguelen Islandlichen metabolitesmolecular phylogeny
Type
Articles
Information
The Lichenologist , Volume 46 , Issue 2 , March 2014 , pp. 175 - 187
Copyright
Copyright © British Lichen Society 2014 

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References

Anslow, W. K. & Raistrick, H. (1941) Synthesis of catenarin (1:4:5:7-tetrahydroxy-2-methylanthraquinone), a metabolic product of species of Helminthosporium . Biochemistry Journal 35: 1006–1010.CrossRefGoogle Scholar
Arup, U. (2006) A new taxonomy of the Caloplaca citrina group in the Nordic countries, except Iceland. Lichenologist 38: 1–20.Google Scholar
Arup, U., Søchting, U. & Frödén, P. (2013) A new taxonomy of the family Teloschistaceae . Nordic Journal of Botany 31: 16–83.Google Scholar
Buckley, T. R., Arensburger, P., Simon, C. & Chambers, G. K. (2002) Combined data, Bayesian phylogenetics, and the origin of the New Zealand cicada genera. Systematic Biology 51: 4–18.Google Scholar
Darriba, D., Taboada, G. L., Doallo, R. & Posada, D. (2012) jModelTest 2: more models, new heuristics and parallel computing. Nature Methods 9: 772.Google Scholar
Ekman, S. (2001) Molecular phylogeny of the Bacidiaceae (Lecanorales, lichenized Ascomycota). Mycological Research 105: 783–797.CrossRefGoogle Scholar
Elvebakk, A. & Moberg, R. (2002) Foliose and placodioid species of the lichen family Physciaceae in southernmost Chile. Lichenologist 34: 311–320.CrossRefGoogle Scholar
Gardes, M. & Bruns, T. D. (1993) ITS primers with enhanced specificity for basidiomycetes – application for the identification of mycorrhizae and rusts. Molecular Ecology 2: 113–118.Google Scholar
Gaya, E., Högnabba, F., Holguin, Á., Molnar, K., Fernández-Brime, S., Stenroos, S., Arup, U., Søchting, U., van den Boom, P., Lücking, R., et al. (2012) Implementing a cumulative supermatrix approach for a comprehensive phylogentic study of the Teloschistales (Pezizomycotina, Ascomycota). Molecular Phylogenetics and Evolution 63: 374–387.Google Scholar
Guindon, S. & Gascuel, O. (2003) A simple, fast and accurate method to estimate large phylogenies by maximum-likelihood. Systematic Biology 52: 696–704.Google Scholar
Lumbsch, H. T., Ahti, T., Altermann, S., Amo de Paz, G., Aptroot, A., Arup, U., Peña, A. B., Bawingan, P. A., Benatti, M. N., Betancourt, L., et al. (2011) One hundred new species of lichenized fungi: a signature of undiscovered global diversity. Phytotaxa 18: 1–127.CrossRefGoogle Scholar
Nicolas, A. N. & Plunkett, G. M. (2012) Untangling generic limits in Azorella, Laretia, and Mulinum (Apiaceae: Azorelloideae): insights from phylogenetics and biogeography. Taxon 61: 826–840. Google Scholar
Olech, M. (2004) Lichens of King George Island, Antarctica. Kraków: Institute of Botany, Jagiellonian University.Google Scholar
Olech, M. & Søchting, U. (1993) Four new species of Caloplaca from Antarctica. Lichenologist 25: 261–269.Google Scholar
Øvstedal, D. O. & Smith, R. I. L. (2001) Lichens of Antarctica and South Georgia. Cambridge: Cambridge University Press.Google Scholar
Posada, D. (2008) jModelTest: phylogenetic model averaging. Molecular Biology and Evolution 25: 1253–1256.CrossRefGoogle ScholarPubMed
Raistrick, H., Robinson, R. & Todd, A. R. (1934) Studies in the biochemistry of micro-organisms. Biochemistry Journal 28: 559–572.Google Scholar
Ronquist, F., Teslenko, M., van der Mark, P., Ayres, D. L., Darling, A., Höhna, S., Larget, B., Liu, L., Suchard, M. A. & Huelsenbeck, J. P. (2012) MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Systematic Biology 61: 539–542.CrossRefGoogle ScholarPubMed
Søchting, U. (1997) Two major anthraquinone chemosyndromes in Teloschistaceae . Bibliotheca Lichenologica 68: 135–144.Google Scholar
Søchting, U. & Lutzoni, F. (2003) Molecular phylogenetic study at the generic boundary between the lichen-forming fungi Caloplaca and Xanthoria (Ascomycota, Teloschistaceae). Mycological Research 107: 1266–1276.Google Scholar
Søchting, U. & Øvstedal, D. O. (1992) Contributions to the Caloplaca flora of the western Antarctic region. Nordic Journal of Botany 12: 121–134.CrossRefGoogle Scholar
Søchting, U. & Sancho, L. G. (2012) Caloplaca magellanica sp. nov., a southern Patagonian parasite on Zahlbrucknerella . Bibliotheca Lichenologica 108: 213–218.Google Scholar
Wagstaff, S. J., Breitwieser, I. & Ito, M. (2011) Evolution and biogeography of Pleurophyllum (Astereae, Asteraceae), a small genus of megaherbs endemic to the subantarctic islands. American Journal of Botany 98: 62–75.Google Scholar
White, T. J., Bruns, T., Lee, S. & Taylor, J. (1990) Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In PCR Protocols: a Guide to Methods and Applications (Innis, M. A., Gelfand, D. H., Sninsky, J. J. & White, T. J., eds): 315–322. San Diego: Academic Press.Google Scholar
Zhou, S. & Stanosz, G. R. (2001) Primers for amplification of mt SSU rDNA, and a phylogenetic study of Botryosphaeria and associated anamorphic fungi. Mycological Research 105: 1033–1044.Google Scholar
Zoller, S., Scheidegger, C. & Sperisen, C. (1999) PCR primers for the amplification of mitochondrial small subunit ribosomal DNA of lichen-forming ascomycetes. Lichenologist 31: 511–516.Google Scholar