Amundsenia austrocontinentalis
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| Amundsenia austrocontinentalis | |
|---|---|
| Scientific classification | |
| Domain: | Eukaryota |
| Kingdom: | Fungi |
| Division: | Ascomycota |
| Class: | Lecanoromycetes |
| Order: | Teloschistales |
| Family: | Teloschistaceae |
| Genus: | Amundsenia |
| Species: | A. austrocontinentalis |
| Binomial name | |
| Amundsenia austrocontinentalis Garrido-Ben., Søchting, Pérez-Ort. & Seppelt (2014) | |
Amundsenia austrocontinentalis is a species of saxicolous (rock-dwelling), crustose lichen in the family Teloschistaceae,[1] and the type species of genus Amundsenia. Found in Antarctica, it was formally described as a new species in 2014 by Isaac Garrido-Benavent, Ulrik Søchting, Sergio Pérez-Ortega, and Rod Seppelt. The type specimen was collected by the last author from Mule Peninsula (Vestfold Hills, Ingrid Christensen Coast), where it was found growing on small stones in glacial till. The species epithet austrocontinentalis refers to its distribution in continental Antarctica.
Amundsenia austrocontinentalis was formally described in 2014, when Isaac Garrido-Benavent, Ulrik Søchting, Sergio Pérez-Ortega, and Rod Seppelt erected both the genus Amundsenia and its Antarctic type species on the basis of a three-gene phylogeny of Teloschistaceae. The analysis placed the genus in subfamily Xanthorioideae as a well-supported sister lineage to Squamulea. The holotype was collected at 8 m elevation on Mule Peninsula in the Vestfold Hills, Ingrid Christensen Coast, from glacial till pebbles.[2]
Although morphologically rather austere, the species is separable from others in its genus and from the superficially similar Charcotiana antarctica. It has flat, pale yellow-orange areoles, thicker apothecial margins and markedly smaller, thin-septate polardiblastic spores (8–13 μm long with a 2–3 μm septum). In contrast, C. antarctica develops coralloid protrusions, deeper orange colours and longer spores with stouter septa. The combination of minute crustose thallus, prosoplectenchymatous proper exciple and chemosyndrome A (parietin-dominated) underpins the generic placement.[2]