Pyrenothrix | |
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Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Fungi |
Division: | Ascomycota |
Class: | Eurotiomycetes |
Order: | Chaetothyriales |
Family: | Pyrenotrichaceae |
Genus: | Pyrenothrix Riddle (1917) |
Type species | |
Pyrenothrix nigra | |
Species | |
Synonyms [1] | |
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Pyrenothrix is a small genus of lichen-forming fungi in the family Pyrenotrichaceae. [2] [3] It comprises two species of filamentous lichens, which are organisms formed by a symbiotic relationship between fungi and photosynthetic partners. The genus is characterized by its unique structure, featuring densely arranged filaments composed of cyanobacteria (blue-green algae) wrapped in fungal threads. Pyrenothrix species form dark greyish-brown growths on various surfaces, with one species found on tree bark and the other on leaves in tropical forests. The genus was circumscribed in 1917 by American scientist Lincoln Ware Riddle, based on specimens collected in Florida. Pyrenothrix is distinguished from other lichens by its intricate cellular structure and reproductive features, including specialized spore-producing structures.
The genus was circumscribed in 1917 by the American lichenologist Lincoln Ware Riddle, with P. nigra assigned as the type, and at the time, only species in the genus. [4] A second species was added in 2005. [5] The oldest lichenized fungal type specimen in the fungal, lichen, and myxomycete collections of the University of North Carolina at Chapel Hill herbarium is Pyrenothrix nigra, collected by Roland Thaxter in Florida in 1897. [6] This material was originally found growing on the bark of scrub oaks at West Palm Beach, Florida. [4]
Lichenothrix is a genus that was proposed by Aino Henssen in 1964, [7] but it has since been folded into synonymy with Pyrenothrix. [8]
Species of Pyrenothrix are characterized by their unique morphology and structure, which sets them apart from other lichen genera. The thallus of Pyrenothrix species is composed of densely arranged, appressed filaments that are not conglutinated . These filaments form a continuous layer that can extend up to 100 mm across in some species. The overall appearance of the thallus is dark greyish brown, though individual filaments appear yellowish to light olive brown under microscopic examination. A distinctive feature of Pyrenothrix is the structure of its photobiont association. The filaments are formed by photobiont threads of Scytonema (a genus of cyanobacteria) wrapped in a sheath of fungal hyphae. This close association creates the characteristic appearance of the lichen thallus. The photobiont cells, when extruded from their gelatinous sheath, appear bluish-green and are typically applanate to rectangular in shape. [5]
The fungal hyphae forming the sheath around the photobiont filaments have a unique structure. They are greatly branched and anastomosing, creating a network that at first glance may appear to form a closed, almost paraplectenchymatous layer. However, closer examination reveals that they consist of distinct, septate hyphae. The individual cells of these hyphae are often curved and terminally inflated, which may represent haustoria. The ascomata of Pyrenothrix are perithecioid , appearing as sessile structures on the thallus. They are spherical to pear-shaped with a short neck, and their color matches the dark greyish brown of the thallus. The size of the perithecia varies between species, ranging from 0.13 to 0.17 mm in diameter in P. mexicana to 0.2–0.3 mm in P. nigra. [5]
The excipulum (peridium) of the perithecia is relatively thin, measuring 10–15 μm in P. mexicana and 15–25 μm in P. nigra. It has a distinctive structure consisting of several layers. The innermost 2–3 layers are composed of very narrow, thin-walled, and periclinally elongate, almost hyaline cells. The median 1–2 layers consist of broader, rather large, thick-walled, and strongly pigmented cells. The outermost 2–3 layers are made up of isodiametric to irregular, thin-walled, and paler cells. This layered structure contributes to the unique characteristics of the Pyrenothrix perithecia. [5]
The asci (spore-bearing cells) in Pyrenothrix are fissitunicate , broadly clavate to saccate in shape. They produce eight ascospores per ascus. The ascospores are fusiform and septate, with the septation pattern differing between species. In P. mexicana, the ascospores are transversally 3-septate, while in P. nigra, they are (sub) muriform with (3–)5 transversal and 0–1 longitudinal septa per segment. This unique combination of morphological and anatomical features distinguishes Pyrenothrix from other lichen genera and contributes to its classification within the Pyrenotrichaceae. [5]
The photobiont of Pyrenothrix nigra has a filamentous cyanobacterial structure with double-false branching, a characteristic traditionally associated with the genus Scytonema . However, research by Robert Lücking and colleagues has suggested that the photobiont might actually belong to the genus Rhizonema . This proposition is considered plausible due to ongoing debates about the reliability of branching patterns as a distinguishing feature between Scytonema and Rhizonema. [9]
Rhizonema, a recently resurrected cyanobacterial genus, was established to classify filamentous, heterocyte-producing photobionts previously thought to be Scytonema, but genetically distinct based on 16S rRNA sequences. The branching patterns in Rhizonema have been observed to include both apparent true branching and false branching, complicating the morphological distinction between these genera. [9]
The exact nature of the photobiont in Pyrenothrix remains uncertain, highlighting the need for more extensive genetic sequencing to clarify the taxonomic boundaries and symbiotic relationships within lichen associations. This uncertainty extends to other lichen symbioses potentially involving Scytonema in its current, more restricted sense. [9]
The cyanobacterial photobionts in Pyrenothrix, whether Scytonema or Rhizonema, are known to produce heterocytes, specialized cells capable of nitrogen fixation. This ability to fix atmospheric nitrogen into biologically usable forms is ecologically significant, potentially contributing to nutrient cycling in the environments where these lichens occur. The filamentous nature of these cyanobionts, characterized by chains of cells (trichomes), allows for the formation of the lichen's distinctive structure. [9]
In Pyrenothrix mexicana, the photobiont has been identified as Scytonema. The thallus is composed of densely arranged, appressed filaments that are not conglutinated . These filaments are formed by unbranched or falsely branched photobiont threads enveloped in a sheath of fungal hyphae. This unique structure creates the characteristic appearance of the lichen thallus. Microscopic examination of P. mexicana reveals that individual filaments appear yellowish to light olive brown. The extruded photobiont threads are bluish, with very applanate cells measuring 2–5 by 10–15 μm. [5]
Gloeoheppiaceae is a family of ascomycete fungi in the order Lichinales. The family contains ten species distributed amongst three genera. Most species are lichenised with cyanobacteria. Species in this family are mostly found in desert areas. Modern molecular phylogenetics analysis casts doubt on the phylogenetic validity of the family, suggesting a more appropriate placement of its species in the family Lichinaceae.
Mazosia is a genus of lichen-forming fungi in the family Roccellaceae.
Gallaicolichen is a fungal genus that contains the single species Gallaicolichen pacificus, a foliicolous (leaf-dwelling) lichen. Originally discovered in Hawaii in 2007, G. pacificus has since been found in various locations across the Pacific, including Australia, New Caledonia, Vanuatu, the Philippines, and Japan. The lichen forms small, pale greenish-yellow to yellowish-grey patches on leaves, typically in mid-altitude forests and along forest edges. G. pacificus is notable for its unique reproductive structures called peltidiangia, which produce disc-shaped propagules (peltidia) for asexual reproduction. Initially, its taxonomic classification was uncertain, but recent discoveries of specimens with sexual reproductive structures have enabled scientists to confidently place it within the family Porinaceae.
Stromatella bermudana is a saxicolous (rock-dwelling) crustose lichen. It is the only species in Stromatella, a monotypic fungal genus in the family Lichinaceae.
Lichens are symbiotic organisms made up of multiple species: a fungus, one or more photobionts and sometimes a yeast. They are regularly grouped by their external appearance – a characteristic known as their growth form. This form, which is based on the appearance of vegetative part of the lichen, varies depending on the species and the environmental conditions it faces. Those who study lichens (lichenologists) have described a dozen of these forms: areolate, byssoid, calicioid, cladoniform, crustose, filamentous, foliose, fruticose, gelatinous, leprose, placoidioid and squamulose. Traditionally, crustose (flat), foliose (leafy) and fruticose (shrubby) are considered to be the three main forms. In addition to these more formalised, traditional growth types, there are a handful of informal types named for their resemblance to the lichens of specific genera. These include alectorioid, catapyrenioid, cetrarioid, hypogymnioid, parmelioid and usneoid.
Lichen morphology describes the external appearance and structures of a lichen. These can vary considerably from species to species. Lichen growth forms are used to group lichens by "vegetative" thallus types, and forms of "non-vegetative" reproductive parts. Some lichen thalli have the aspect of leaves ; others cover the substrate like a crust, others such as the genus Ramalina adopt shrubby forms, and there are gelatinous lichens such as the genus Collema.
Mastodia is a genus of lichen-forming fungi in the family Verrucariaceae. It has six species.
Dictyonema album is a species of basidiolichen in the family Hygrophoraceae. It is found in Mauritius, where it grows as an epiphyte on shrubs.
Dictyonema ramificans is a basidiolichen species in the family Hygrophoraceae. Discovered in 2010 in the Galapagos Islands, it was formally described as a new species in 2017 by lichenologists Manuela Dal-Forno, Alba Yanez-Ayabaca, and Robert Lücking. Its species epithet is derived from the branching pattern of the fibrils that form a net-like structure, giving it an arachnoid (cobweb-like) appearance. This species has only been found in the humid zone of Santa Cruz Island, growing exclusively on bryophytes. While it is similar to other Dictyonema species, it differs in its unique fibril branching pattern and erect arachnoid structure.
Heppia arenacea is a species of terricolous (ground-dwelling) lichen in the family Lichinaceae. Discovered in Yemen, it is characterized by its sand-coloured thallus and the incorporation of soil particles throughout its vegetative parts. The lichen is found in soil crust communities over limestone and basaltic rock in desert habitats, as well as in partially sheltered areas between large boulders.
Dictyonema aeruginosulum is a species of basidiolichen in the family Hygrophoraceae. Characteristics of the lichen include its distinctive finger-like projections and blue-green hue. It is distinguishable from its closest relatives by its unique morphology and the absence of clamp connections in its structure. Dictyonema aeruginosulum is an epiphyte, forming thick mats on tree trunks within rainforest regions. The species was first identified in Costa Rica's Tenorio Volcano National Park, and it has only been recorded from this location.
Dictyonema krogiae is a species of basidiolichen in the family Hygrophoraceae. It is found in Kenya, where it grows as an epiphyte on trees. It is often found in association with other lichens, such as Parmotrema, and bryophytes, such as Frullania. A main characteristic that distinguishes it from other closely related species is its clearly defined internal layers, including its contrasting dense photobiont layer and a loose lower cortex.
The Pyrenotrichaceae are a small family of fungi in the order Chaetothyriales. It contains two genera, and a total of six species. The genus Pyrenothrix has two species of bark- or leaf-dwelling lichens, while Neophaeococcomyces has four species of saprobic fungi.
Cyanoporina is a fungal genus in the division Ascomycota. The relationship of this taxon to other taxa within the division is unknown, and it has not yet been placed with certainty into any class, order, or family. The genus is monospecific, containing the single species Cyanoporina granulosa, a crustose lichen found in West Java, Indonesia.
Leptogidium is a genus of lichen-forming fungi in the family Pannariaceae. It has six species.
Saxiloba is a genus of lichen-forming fungi in the family Porinaceae. It comprises three species of saxicolous (rock-dwelling) placodioid lichens, known from disjunct locations in the Caribbean, Hawaii, and Brazil. The genus was circumscribed in 2020 to accommodate species with a distinctive placodioid thallus featuring unique surface patterns and internal crystal structures. Saxiloba lichens are characterised by their flattened, leaf-like thalli with marginal lobes, growing tightly appressed to rock surfaces. They have a complex internal structure, including large crystal clusters embedded within the photobiont layer, which may be an adaptation for light management in their typically shaded habitats.
Gloeoheppia is a genus of lichen-forming fungi in the family Gloeoheppiaceae. It comprises five species. The genus is distinguished from similar-looking lichens like Heppia by its internal structure, the nature of its photobiont, and details of its reproductive structures.
Flabelloporina is a fungal genus in the family Porinaceae. It consists of a single species, Flabelloporina squamulifera, which grows on tree bark in tropical rainforests. The lichen was first discovered in Costa Rica in 2013 and later found in Brazil, suggesting it may be more widespread in South and Central American wet forests. Flabelloporina is distinguished by its unique thallus structure, which produces numerous small, fan-shaped outgrowths called squamules. These structures, along with its black fruiting bodies and internal features, set it apart from related lichens. Originally classified in the genus Porina, genetic analysis in 2018 revealed it to be distinct, leading to the creation of the new genus Flabelloporina. The lichen typically inhabits the lower levels of humid forests, where it can sometimes extensively cover individual tree trunks.
Pseudopeltula is a genus of lichen-forming fungi in the family Gloeoheppiaceae. Established in 1995 by the lichenologist Aino Henssen, the genus currently includes four recognised species. These small cyanolichens are characterised by their squamulose (scaly) to peltate (shield-shaped) thalli, which lack a lower cortex and are attached to the substrate by rhizines. A key feature of Pseudopeltula is its complex apothecia, which have hymenia that often become divided by sterile tissue as they mature. The genus is primarily found in arid and semi-arid regions of North America, Mexico, and the Caribbean, where species typically grow on soil, rock, or thin soil over rock, often forming part of biological soil crusts in desert environments.