Message - 7th IAL Symposium
Message - 7th IAL Symposium
Message - 7th IAL Symposium
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The 7 th International Association for Lichenology <strong>Symposium</strong> 2012<br />
(1I-P2) Submission ID: <strong>IAL</strong>0083-00001<br />
TOWARDS A MOLECULAR PHYLOGENY OF LICHENICOLOUS DACAMPIACEAE<br />
(DOTHIDEOMYCETES, ASCOMYCOTA)<br />
Döring H. 1 , Atienza V. 2<br />
1 Mycology Section, Royal Botanic Gardens, Kew, Richmond, United Kingdom<br />
2 Departamento de Botanica, Universitat de Valencia, Burjasot, Valencia, Spain<br />
The family Dacampiaceae comprises about 15 genera. Eight genera (Clypeococcum, Dacampia, Kalaalia,<br />
Polycoccum, Pseudonitschkia, Pseudopyrenidium, Pyrenidium, Weddellomyces) include mainly or exclusively<br />
lichenicolous species. The family is currently classified within Pleosporales in the Dothideomycetes.<br />
However, no molecular data exist to test the phylogenetic placement of any of the lichenicolous taxa. We aim to<br />
generate a hypothesis of the phylogenetic position of lichenicolous Dacampiaceae and to test the monophyly of<br />
the group. Recent material of such inconspicuous fungi is usually not readily available for laboratory work, cultures<br />
cannot easily be obtained from obligate parasites, and it is likely that any extraction from an infected lichen<br />
specimen contains a mixture of DNAs of at least two ascomycetes. For DNA extractions we used minute portions<br />
of the samples that have been carefully prepared and cleaned under a dissecting microscope to contain as much<br />
material of the lichenicolous fungi as possible. Different PCR primer combinations for the nuclear ribosomal DNA<br />
genes were tested, and where possible directly sequenced. In many cases, as expected, mixed PCR products<br />
required sequencing via DNA cloning. It proved difficult to generate DNA sequence data of sufficient quality and<br />
quantity. We are going to report on the diversity of fungal sequences obtained from samples of lichenicolous<br />
Dacampiaceae. Our study highlights the elaborate process of obtaining reliable DNA sequence data for a larger<br />
amount of such species. The routine inclusion of sequence data in the taxonomic description for new species, as<br />
currently discussed, appears to be an extremely difficult task for these fungi. In some cases a single sequence<br />
clustering within Dothideomycetes was obtained straight away. However, despite careful preparation from some<br />
DNA extractions only sequences belonging to the host lichen could be retrieved, and in other cases cloning was<br />
necessary to separate different fungal sequences. Some sequences originated from obviously unrelated fungi,<br />
but from some extractions multiple sequences with affinity to Dothideomycetes were gathered. Therefore, multiple<br />
samples are needed to confirm the identity of a specific DNA sequence as belonging to the Dacampiaceae<br />
species in question. The phylogenetic position of some lichenicolous Dacampiaceae species will be shown.<br />
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