Peltula Radicata

''Peltula'' is a genus of small dark brown to olive or dark grey squamulose lichens. These lichens typically grow on rocks in arid and semi-arid environments worldwide. They consist of a fungus living in symbiosis with a photosynthetic partner, specifically a cyanobacterium of the genus '' Chroococcidiopsis''. ''Peltula'' is the only genus in the family Peltulaceae, which belongs to the Lichinomycetes, a class of fungi that form lichens. The genus includes about 50 recognised species, which exhibit a variety of growth forms ranging from flat and crust-like to more complex, leaf-like structures. ''Peltula'' lichens play important ecological roles in harsh environments, contributing to soil stability and nutrient cycling.

To cope with their challenging habitats, ''Peltula'' species have evolved various adaptations. These include specialised protective layers and the ability to withstand both drought and flooding. The thalli of ''Peltula'' lichens are typically small, with a stratified structure consisting of an upper , a , a medulla, and usually a lower . Peltulaceae generally lack secondary metabolites, which distinguishes them from many other lichen families. The genus has a cosmopolitan distribution, with members found across various continents, occupying diverse including rocks, soil, and occasionally tree bark. Molecular phylogenetics studies have significantly altered the classification of these lichens. Formerly separate genera are now incorporated into ''Peltula'', rendering Peltulaceae a monogeneric family.

Systematics

Historical taxonomy

Genus ''Peltula'' was circumscribed by the Finnish lichenologist William Nylander in 1853. He assigned the desert soil lichen '' Peltula radicata'' as the type, and at that time, only species. In his original description of ''Peltula radicata'', Nylander characterised it as having a rust-brown, peltate thallus measuring at least 3 mm wide, with an irregularly and sparsely grooved surface. He noted that the thallus had a centrally depressed, umbilicate attachment, fixed to the substrate by a few pale, long, and strong rhizines. Nylander described the apothecia as disc-shaped and the same colour as the thallus, initially almost endocarpoid, but expanding significantly with age and featuring a depressed thalline margin. He observed that the asci contained numerous spores, 8–48 or possibly more. The type (biology) was found growing on sandy soil near Biskra, Algeria, alongside ''Lecanora endocarpa''. In establishing the new genus ''Peltula'', he distinguished it from other Lecanorine genera by its thallus being attached below with long, central rhizines. In 1890, Vainio proposed that ''Peltula'' should be considered a section of the genus ''Heppia'' rather than an independent genus.

For decades, the genus ''Peltula'' saw limited use. Many species now classified under ''Peltula'' were previously placed in ''Heppia''. Vilmos Kőfaragó-Gyelnik added some species to ''Peltula'' in 1935. The family was Peltulaceae proposed by the German lichenologist Burkhard Büdel in 1986. He identified four types of growth morphologies in the family: leaf-like, squamulose, crustose and fruticose. The genera ''Phyllopeltula'' and ''Neoheppia'' were created as segregates of ''Peltula'' to contain species with differences in their cortex morphology and substratum. ''Neoheppia'' was introduced by Alexander Zahlbruckner in 1909 for ''N. brasiliensis'', which had a crustose thallus attached to its substrate by all parts of its lower surface. ''Phyllopeltula'' differed from the typical ''Peltula'' morphology with subfoliose-compound thalli. These genera were included as part of the Peltulaceae.

Phylogenetics

Egea (1989) and Büdel (1987) made early attempts to establish phylogenetic lineages within ''Peltula'' based on morphology. Egea identified two major evolutionary lineages based primarily on substratum fixation, while Büdel described two groups of closely related species based on thallus morphology. However, these classification attempts remained controversial due to the morphological variability within the genus.

Early molecular phylogenetics work (2001) showed that the family was monophyletic. More recent molecular studies have led to a significant revision of the family's taxonomy. A comprehensive study by Kauff and colleagues (2018) analysed six genetic loci from 37 of the 47 species classified within Peltulaceae at the time. The results of this analysis revealed that ''Phyllopeltula'' and ''Neoheppia'' are not monophyletic and are nested within the genus ''Peltula''. As a consequence of these findings, ''Phyllopeltula'' and ''Neoheppia'' have been subsumed into ''Peltula'', making Peltulaceae a monogeneric (single-genus) family. The family now includes about 50 recognised species, all within the genus ''Peltula''. The study also highlighted significant challenges in species delimitation within ''Peltula''. Traditional morphological characters, such as growth forms and thallus anatomy, which were previously used to delimit genera and species within the family, have been shown to be unreliable indicators of phylogenetic relationships. Significant differences in thallus shape and structure were seen within several species, further complicating classification efforts based on morphology alone.

Naming

The genus name is derived from the Latin , , alluding to the shape of the squamules. In North America, the colloquial name "rock olives" refers to members of this genus, highlighting both their colour and typical substrate. Several North American species with common names include the cylindrical, powdery, common, stuffed, and giant rock-olives.

Description

Peltulaceae members exhibit a diverse range of thallus morphologies. Thalli are typically small, ranging from minute to larger compound structures. Most species possess a stratified () thallus structure, consisting of an upper , a , a medulla, and usually a distinct lower . The epinecral layer, often yellowish to brown, provides protection and its development is influenced by light intensity. The medulla in many species contains air spaces of various sizes, while some taxa lack a lower cortex or medullary cavities.

The growth forms of Peltulaceae can be categorised into six types based on morphology and anatomy. ''Peltate-umbilicate'' forms are often singular thalli, rarely compound, attached by an or central strand of hyphae. Squamulose-semifruticose forms are characterised by large medullary cavities. Squamulose-compound forms are rarely singular. Subfoliose, compound forms lack medullary cavities and a lower cortex. Crustose- forms have no medullary cavities or lower cortex, but possess a deeply penetrating cyanobiont layer. Finally, a unique crustose form is found in ''P. inversa'', which exhibits an inverse thallus anatomy.

Peltulaceae are exclusively associated with unicellular cyanobacterial photobionts, predominantly of the genus '' Chroococcidiopsis''. Apothecia are common in most species, with a few exceptions, and they are in form and typically in the thallus. The family is characterised by uniform reproductive structures across all species, including polysporous asci with a distinctive gelatinous sheath, and , single-celled, colourless spores. The ascospores range in shape from more or less spherical, to ellipsoidal, to , and measure 3–12 by 2–6 μm. The asci are -, which means have they a single-layered wall with a beak-like tip. Pycnidia, conidiophores, and pycnospores are also consistent in structure throughout the family; the conidia are hyaline, oval to in shape, and have dimensions of 1.5–4.3 by 0.5–2.5 μm. Vegetative reproductive structures such as soredia and isidia occur in a small number of species.

Unlike many other lichen families, Peltulaceae generally lack secondary metabolites (lichen products). An exception is '' Peltula langei'', which produces a yellow pigment similar to myeloconon C. The thallus structure of Peltulaceae species shows various adaptations to their predominantly arid and semi-arid habitats. The epinecral layer shields the photobiont from intense sunlight, while different growth forms are associated with varying water availability. Some species, particularly those with squamulose to semifruticose thalli and large medullary cavities, are adapted to temporarily inundated habitats. These morphological and anatomical features reflect the family's successful adaptation to challenging environmental conditions, allowing them to grow in a range of ecological niches from desert rocks to occasionally submerged surfaces.

Habitat, distribution, and ecology

Peltulaceae has a cosmopolitan distribution, with members found across various continents. These lichens are particularly well-adapted to arid and semi-arid environments. Despite their preference for dry habitats, some species have been documented in areas with more moderate climates, including locations as far north as Sweden and as easterly as the Baikal region of Siberia.

Five species of ''Peltula'' are known to occur in India. About 20 species have been recorded in China, and 18 from North America north of Mexico. Fifteen species occur in Australia, and eleven species were reported to occur in East Africa.

Peltulaceae species occupy a diverse array of substrates. Many members of the family are saxicolous, growing on rock surfaces. These rock-dwelling species can be found on various geological formations, from exposed cliff faces to small stones. Some Peltulaceae have evolved to grow on soil, while others, such as '' Peltula corticola'', have adapted to a corticolous lifestyle, growing on tree bark. In an example of niche specialisation, '' P. inversa'' exhibits a hypolithic habit, growing on the underside of quartz rocks.

Several ''Peltula'' species show remarkable substrate tolerance. A 2024 study in northeastern Brazil found that '' P. obscurans'', '' P. euploca'', and '' P. impressa'' were able to colonise rocks with high levels of natural gamma radiation, while most other lichen genera were absent from these uranium-rich substrates. In India, burnt clay tiles, commonly used for roofing, support both '' P. euploca'' and '' P. patellata''. Under constant sun exposure for most of the day, the lichens develop a thickened upper cortex that both helps to retain moisture and acts as a photoprotectant.

The family's adaptability is further exemplified by the range of specific microhabitats they occupy. Some species prefer inclined rock surfaces, while others colonise flat rock expanses. Certain Peltulaceae species have developed the ability to withstand periodic inundation, allowing them to inhabit seepage areas on rocks that are occasionally flooded.

The morphological and anatomical features of Peltulaceae species often correspond to their specific environmental conditions. For instance, the development of the , which provides protection to the photobiont, is influenced by the intensity of light in the habitat. The various growth forms observed in the family, from peltate to crustose, are closely linked to water availability in their respective environments. Species that experience occasional submersion often possess large medullary cavities, an adaptation that likely aids in gas exchange and water relations during both dry and inundated periods.

As primary producers in often-sparse environments, they contribute to soil stability, nutrient cycling, and provide microhabitats for other organisms, playing a role in the biodiversity of challenging climatic regions.

Species

, Species Fungorum (in the Catalogue of Life) accepts 35 species in ''Peltula'', although 66 unique species names have been proposed in the genus.

*'' Peltula africana''
*'' Peltula anthracina''
*'' Peltula auriculata''
*'' Peltula bolanderi''
*'' Peltula boletiformis''
*'' Peltula brasiliensis''
*'' Peltula capensis''
*'' Peltula cataractae''
*'' Peltula clavata''
*'' Peltula confusa'' – China
*'' Peltula congregata''
*'' Peltula coriacea''
*'' Peltula corticola''
*'' Peltula crispatula''
*'' Peltula cylindrica''
*'' Peltula daurica''
*''Peltula euploca''
*'' Peltula farinosa''
*'' Peltula guepinii''
*'' Peltula hassei''
*'' Peltula imbricata''
*'' Peltula impressa''
*'' Peltula impressula''
*'' Peltula inversa''
*'' Peltula japonica''
*'' Peltula koflerae''
*'' Peltula leptophylla''
*'' Peltula lingulata''
*'' Peltula lobata'' – Europe
*'' Peltula lobulata'' – China
*'' Peltula marginata''
*'' Peltula obscurans''
*'' Peltula obscuratula''
*'' Peltula omphaliza''
*'' Peltula patellata''
*'' Peltula placodizans''
*'' Peltula polycarpa'' – China
*'' Peltula polyphylla'' – China
*'' Peltula psammophila''
*'' Peltula pseudoboletiformis'' – China
*'' Peltula radicata''
*'' Peltula richardsii''
*'' Peltula rodriguesii''
*'' Peltula ruinicola''
*'' Peltula santessonii''
*'' Peltula sonorensis''
*'' Peltula steppae''
*'' Peltula submarginata'' – China
*'' Peltula subpatellata'' – China
*'' Peltula tenebrata''
*'' Peltula tenuis''
*'' Peltula tortuosa''
*'' Peltula umbilicata''
*'' Peltula zahlbruckneri''
*'' Peltula zabolotnoji''
''Peltula langei'' , a Western Australian species described as new in 1997, was not validly published. The original binomial for ''Peltula oleifera'' (''Heppia oleifera'' H.Magn.) had already been reduced to synonymy with '' Peltula impressula'' in 1981, a decade before Wei erroneously proposed a transfer to ''Peltula''.

References

{{Taxonbar , from1=Q7161784 , from2=Q7161785 , from3=Q6992969 , from4=Q107289586 , from5=Q7189337

Lichinomycetes
Lichinomycetes genera
Lichen genera
Taxa named by William Nylander (botanist)
Taxa described in 1853