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| Xanthoria parietina | |
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| Yellow-orange Xanthoria parietina thallus growing on tree bark, surrounded by Physcia adscendens (greyish), and Trentepohlia algae | |
Scientific classification 
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| Domain: | Eukaryota |
| Kingdom: | Fungi |
| Division: | Ascomycota |
| Class: | Lecanoromycetes |
| Order: | Teloschistales |
| Family: | Teloschistaceae |
| Genus: | Xanthoria |
| Species: | X. parietina
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| Binomial name | |
| Xanthoria parietina | |
| Synonyms[1][2] | |
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List
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Xanthoria parietina is a common and widespread lichen-forming fungus in the family Teloschistaceae. Commonly known as the yellow wall lichen, common orange lichen, or maritime sunburst lichen, this leafy lichen is known for its vibrant yellow to orange coloration and environmental adaptability. First described by Carl Linnaeus in 1753, it has become one of the most thoroughly studied lichens, contributing significantly to scientific understanding of lichen biology. Unlike many lichens that are sensitive to pollution, X. parietina grows in diverse habitats—including coastal rocks, urban walls, and tree bark—even in areas with high levels of air pollution and excess nitrogen. Its structure consists of small, overlapping lobes that typically measure less than 8 cm (3+1⁄8 in) across, with coloration that varies from bright orange in sun-exposed locations to greenish-yellow in shaded environments.
The lichen represents a symbiotic partnership between a fungus and green algae of the genus Trebouxia. Its distinctive orange-yellow color comes from parietin, an anthraquinone pigment that accumulates in the outer cortex and serves as a natural sunscreen, protecting the algal partner from excessive light and ultraviolet radiation. Unlike many lichens that reproduce through specialized vegetative structures, X. parietina primarily relies on sexual reproduction through cup-shaped fruiting bodies (apothecia), each of which can release up to 50 spores per minute under humid conditions. When fungal spores germinate, they initially form preliminary associations with common free-living algae in their vicinity. Additionally, the fungus can recruit compatible algal cells from neighboring lichen thalli—essentially extracting these partners—to help establish a complete symbiotic relationship.
Native across Europe, parts of Asia, and coastal North Africa, X. parietina has a more limited and primarily coastal distribution in North America and Australia, where genetic evidence suggests human-mediated introduction. In recent decades, it has expanded inland in these regions, particularly in urban environments and areas affected by agricultural runoff, road salt application, and nitrogen deposition. The lichen grows slowly (averaging 2.6 mm (1⁄8 in) per year) but possesses considerable regenerative abilities, with fragments capable of developing into new thalli. It participates in a complex web of ecological interactions, hosting at least 41 species of lichen-dwelling fungi, while certain gastropods and microscopic rotifers contribute to its dispersal by consuming and excreting viable spores.
The species has high diversity even within local populations, with distinct patterns linked to both geographic location and substrate type. This genetic variability, combined with the lichen's flexible associations with different photobiont strains, contributes to its ecological success. X. parietina serves as a bioindicator for monitoring air quality due to its capacity to accumulate environmental contaminants. Historically, it was used in folk medicine to treat jaundice and as a natural dye source for textiles. More recently, it has become a subject of astrobiology research, where it survives Mars-like environments, space vacuum, cosmic radiation, and extreme cold. This resilience has established X. parietina as a model organism in both environmental monitoring and space exploration research.