2006) Most photobiont species, especially from the genus Treboux

2006). Most photobiont species, especially from the genus Trebouxia, are cosmopolitan with more or less broad ecological preferences (Fernandez-Mendoza et al. 2011; Ruprecht et al. 2012) and this was true for the most commonly detected clades in this study. However, several distinct and strongly supported clades of the genera Asterochloris and Trebouxia (Online Resource 2, Figs. 2, 3) do not seem to be cosmopolitan, e.g. T. sp URa8 which, to date,

has only been found at Tabernas. This clade is sister to T. gigantea, a photobiont which is widely distributed in temperate habitats (Ettl and Gärtner 1995). This is a somewhat similar situation to that found in PLX-4720 datasheet another study of the cosmopolitan photobiont T. jamesii. Ruprecht et al. (2012) which showed that one sub-clade was only present in the most extreme GDC-0973 mouse habitat of the cold deserts in the Darwin Area (Antarctica). More investigations with much more extended taxon sampling needs to be done in order to decide which adaptations have occurred in response to extreme climatic conditions or particular ecological niches, and which CFTRinh-172 in vitro speciation model

applies. Although no special ecological preferences are described in the literature for the genus Asterochloris (Peksa and Skaloud 2011), no representatives of this genus were found at the Tabernas desert in SE-Spain. Asterochloris species were, however, present at the more temperate and high alpine areas. There are at least two possible interpretations for these findings: Either the Asterochloris photobionts of P. decipiens cannot cope with the desert climate or the P. decipiens present at Tabernas preferentially selects other photobiont species. Attempting to answer this question is part of another study within the framework of the SCIN-project. The Clostridium perfringens alpha toxin highly variable occurrence of different photobiont types in association with the same mycobiont, P. decipiens, across all sampled habitats supports the opinion that flexibility in photobiont choice may influence the ecological amplitude of lichens (Peksa and Skaloud 2011). Low photobiont specificity

is already known for several lichen species that show a wide ecological amplitude, e.g. Lecanora rupicola, and it appears that the key BSC lichen P. decipiens might employ a similar strategy for colonizing highly diverse habitats. In addition, the improved molecular techniques developed here can be important tools for future surveys of photobionts. Our results provide basic information that can underpin conservation measures to protect this highly specialized and diverse community of organisms that colonises and protects the soil surface in large areas of the world. Acknowledgments We are very thankful to Prof. T.G. Allan Green (Universidad Complutense Madrid) for advice and support. This study is part of the SCIN-project (Soil Crust InterNational—Understanding and valuing biological soil protection of disturbed and open land surfaces, http://​www.​soil-crust-international.

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