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Message - 7th IAL Symposium

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Lichen: from genome to ecosystem in a changing world<br />

3A: Molecular phylogenetics<br />

(3A-O1) Submission ID: <strong>IAL</strong>0273-00001<br />

THE DATING OF FUNGI AND PLANTS<br />

Lutzoni F. 1 , Magallon S. 2 , Nowak M. 1 , Alfaro M. 3 , Mcdonald T. 1 , Miadlikowska J. 1 , Reeb V. 1<br />

1 Department of Biology, Duke University, Durham, United States<br />

2 Instituto de Biologia, Universidad Nacional Autonoma de Mexico, Mexico City, Mexico<br />

3 Department of Ecology and Evolutionary Biology, University of California, Los Angeles, United States<br />

The lichen symbiosis is one of many successful interactions between fungi and plants. The omnipresence<br />

of these interdependent heterotrophic-autotrophic associations at spatial and temporal scales, and ranging<br />

from mutualism to parasitism, suggests a strongly linked coevolution of these two kingdoms. If true, major<br />

adaptive radiations of plants and fungi should be mostly synchronized. In this study we have estimated divergence<br />

time of the fungi and land plants independently and inferred the occurrence of drastic shifts in rates of<br />

diversification across both chronograms. The combination of both analytical results enabled us to determine the<br />

synchronicity of these shifts in species diversification that likely occurred during the evolution of fungi and plants.<br />

Lichen-forming ascomycetes originated during one of the most spectacular adaptive radiations of the fungi, and<br />

of the plant kingdom. The origin of ascolichens is more recent than previously expected within the context of<br />

plant evolution, and is associated with the origin and radiation of hyperdiverse endophytic and endolichenic fungi<br />

interacting symbiotically with photosynthetic cells of plants as well as photoautotrophic prokaryotic and eukaryotic<br />

cells (photobionts) found in lichens. The origin of these Leotiomyceta fungi interacting with photosynthetic<br />

cells of plants are associated with the acquisition of an ammonium transporter/ammonia permease (AMTP) gene<br />

from hyperthermophilic chemolithoautotrophic prokaryotes via horizontal gene transfer. Balanced transport of<br />

nitrogen among lichen symbionts could be essential for the establishment and maintenance of this symbiosis,<br />

especially in nitrogen limiting environments.<br />

3A-O<br />

(3A-O2) Submission ID: <strong>IAL</strong>0174-00001<br />

DIVERSIFICATION OF LICHEN-FORMING ASCOMYCETES<br />

Nelsen M. P. 1 , Lücking R. 2 , Lumbsch H. 2 , Ree R. 2<br />

1 Committee on Evolutionary Biology, Department of Botany, University of Chicago, Field Museum,<br />

Chicago, Illinois, United States<br />

2 Department of Botany, The Field Museum, Chicago, United States<br />

The disparity in species richness across fungal lineages is striking. Within the fungal class Lecanoromycetes<br />

(Ascomycota), this unevenness is especially pronounced, with the number of species per family ranging<br />

from under 15 to nearly 2,500. Here potential explanations for this imbalance, initially focusing on clade age and<br />

diversification rate, are explored. Clade age showed little correlation with clade richness, while a strong correlation<br />

was observed between net diversification rate and clade richness. A number of families, such as Parmeliaceae<br />

and Cladoniaceae, were identified as having exceptionally high diversification rates, while a number of<br />

families with low species richness, such as Gypsoplacaceae and Miltideaceae had exceptionally low diversification<br />

rates. Finally, we attempt to identify potential sources of variation in diversification rates across Lecanoromycetes.<br />

48

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