Xylopsora canopeorum

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Xylopsora canopeorum
Xylopsora canopeorum (10.3897-mycokeys.30.22271) Figure 2.jpg
Scale bar: 1 mm
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Fungi
Division: Ascomycota
Class: Lecanoromycetes
Order: Umbilicariales
Family: Umbilicariaceae
Genus: Xylopsora
Species:
X. canopeorum
Binomial name
Xylopsora canopeorum
Timdal, Reese Næsborg & Bendiksby (2018)
Xylopsora canopeorum
Holotype: Big Basin Redwoods State Park, California, USA [2]

Xylopsora canopeorum is a squamulose (scaly), corticolous (bark-dwelling) lichen species in the family Umbilicariaceae. [3] Discovered in the canopies of Sequoia sempervirens (coast redwoods) in California, United States, it was formally described as new to science in 2018. It is endemic to the central coastal region of California, living within the unique ecosystems of Big Basin Redwoods State Park and Armstrong Redwoods State Natural Reserve, areas known for their ancient coast redwood forests. The lichen evolves from a crust-like to scale-like form, developing into coral-like crusts as it matures, complemented by distinctive flat, black reproductive discs . This species has varying greyish-green to medium brown coloration and occasionally forms soralia, which release powdery reproductive propagules called soredia. Xylopsora canopeorum is distinguished from closely related species by its smaller, partly coral-like squamules (scales), the occurrence of soralia on its surface, and in some specimens, the presence of both thamnolic and friesiic acids within the thallus.

Contents

Xylopsora canopeorum was declared endangered by the IUCN in 2021 due to its habitat specialization, severe fragmentation of its range from historic logging, and increased vulnerability to high-intensity wildfires exacerbated by climate change. Conservation efforts are needed for its survival, with accurate knowledge about its distribution hampered by the challenges of accessing the canopy and the need for specialized observation techniques.

Taxonomy

The lichen was first scientifically described in 2018 by the lichenologists Einar Timdal, Mika Bendiksby, and Rikke Reese Næsborg. The type specimen was collected by Bendiksby from Big Basin Redwoods State Park, California, at an elevation of 341 m (1,119 ft); there, it was found growing on the bark of a main trunk of an old Sequoia sempervirens more than 100 cm (40 in) in diameter. [2] The species epithet canopeorum is derived from the species' habitat, specifically highlighting its discovery within the canopies of ancient redwood forests. [2]

Molecular phylogenetics analyses, using sequence alignments derived from both nuclear (ITS and LSU) and mitochondrial (SSU) ribosomal DNA data, have robustly positioned X. canopeorum within the X. caradocensisX. friesii clade. These conclusions are supported by Bayesian inference, maximum likelihood estimation, and maximum parsimony methods, confirming the species as a distinct evolutionary lineage. To achieve these results, the research incorporated both manual and automated methods for establishing multiple sequence alignments, which are particularly challenging for non-coding DNA regions with variable lengths. [2]

Description

Xylopsora canopeorum has a thallus that ranges from crust-like to scale-like in appearance, with individual scales ( squamules ) measuring up to 0.5 mm in diameter. These scales often evolve into a coral-like crust as the lichen ages, initially adhering flatly to the surface before standing upright in a manner that seeks the direction of gravity (geotropically imbricate). Sporadically, the lichen forms soralia, structures that release powdery reproductive propagules called soredia , appearing in patches and bearing a bluish hue. [2]

The surface of the thallus shows a color palette ranging from greyish-green to medium brown, with a matte finish. Its edges may be finely notched or cut and are the same color as the rest of the upper surface. The uppermost layer ( cortex ) of the thallus is relatively thin, reaching up to 15  micrometers (μm), though it typically lacks a well-defined structure. [2]

Reproductive structures (apothecia), which are common in this species, appear as flat, black discs without a powdery coating ( epruinose ), measuring up to 0.6 mm across. The edges of these discs remain distinct and may either be smooth or somewhat wavy. The supporting structure of the apothecia ( exciple ) consists of densely packed fungal filaments, darker on the outer rim and lighter towards the center, without crystal formations. The tissue layer beneath the spore-producing layer (hymenium) and the tissue base ( hypothecium ) share a pale olivaceous brown color, while the very top layer ( epihymenium ) is dark reddish brown, also devoid of crystals. The spore-producing cells (asci) are club-shaped, approximately 30 μm tall, featuring a thin amyloid structure at the center covered by a cap, containing orange pigment when young. [2]

The spores themselves are ellipsoidal and clear, containing orange pigment when young, measuring 4–7 by 2.5–4.5 μm. Structures known as pycnidia, which would produce asexual spores, have not been observed in this species. [2]

Chemically, X. canopeorum is characterized by the presence of friesiic acid as its major component, with thamnolic acid varying from absent to a minor component. The thallus reacts to certain chemical spot tests, changing color to yellow in the presence of para-phenylenediamine (PD) and potassium hydroxide (K), while it shows a bluish-white fluorescence under ultraviolet light (UV+). [2]

Similar species

Xylopsora canopeorum has distinctive morphological characteristics when compared to its close relatives X. caradocensis and X. friesii , particularly in the size and development of its squamules. These squamules are smaller in X. canopeorum, typically under 0.5 mm in diameter, and tend to form a coralloid crust or develop into soralia as they mature. In contrast, both X. caradocensis and X. friesii feature squamules that are significantly larger, reaching diameters of up to 1.0 to 1.5 mm, and lack the sorediate formations seen in X. canopeorum. [2]

The texture and orientation of the squamules also vary between these species. X. caradocensis squamules present a bullate (blistered) or irregularly ascending profile, whereas X. friesii's squamules are more uniform, adhering closely to the substrate or slightly ascending. Furthermore, the ascospores of X. caradocensis are longer, ranging from 6.5 to 14 μm in length, and often show one or three septa, distinguishing them from the typically non-septate and shorter ascospores of X. canopeorum, which more closely resemble those of X. friesii in size. Chemically, both X. caradocensis and X. friesii are known to contain only friesiic acid, setting them apart from the possible chemical diversity observed in X. canopeorum. [2]

Distribution and habitat

Xylopsora canopeorum grows on the bark of ancient coast redwoods. Coast Redwood Stand in Big Basin State Park.jpg
Xylopsora canopeorum grows on the bark of ancient coast redwoods.

Xylopsora canopeorum is exclusively found in the central coastal region of California, with confirmed specimens collected within Big Basin Redwoods State Park and Armstrong Redwoods State Natural Reserve. These locations, situated respectively 11 km (6.8 mi) and 18 km (11 mi) away from the Pacific Ocean, are notable for their ancient coast redwood forests, providing a unique ecosystem for this lichen species. [2] The exploration of forest canopies remains limited, largely due to the challenges and specialized skills and equipment needed to access the treetops. Chaenotheca longispora is another lichen found from a similar location in a California State Park and reported as a new species in 2019. [4]

In terms of its ecological niche, X. canopeorum grows on the coarse and fibrous bark of large coast redwood trees, sometimes extending to charred areas of the bark. This lichen is predominantly found at elevations ranging from 5 to 75 m (16 to 246 ft) above the forest floor, growing on the venerable and robust bark surfaces of the redwoods' main trunks. The presence of Xylopsora canopeorum is often associated with a community of other lichen species, including Carbonicola anthracophila , Fulgidea oligospora , F. sierrae , Hertelidea botryosa , and Hypocenomyce scalaris , which share the surfaces offered by the ancient trees of these old-growth forests. [2]

Conservation

In 2021, Xylopsora canopeorum was assessed by the International Union for Conservation of Nature as an endangered species in its global IUCN Red List. The lichen is facing significant threats primarily due to its specialized habitat in the old-growth coast redwood forests of Northern California. With a natural range that has dwindled to about 5% of its original size due to historic logging, the species' populations are not only severely fragmented but also continually at risk. This fragmentation has been exacerbated by high-intensity wildfires, such as the one in 2020 that affected its type locality, contributing to a decline in both the quality and extent of its habitat. Climate change poses additional threats by increasing the frequency and severity of such wildfires, potentially leading to further losses and extirpation from significant portions of its range, including a potential 97.7% reduction in extent of occurrence and a 33% reduction in area of occurrence if lost from Big Basin Redwoods State Park. Conservation efforts are needed to mitigate the impacts of climate change and protect the remaining old-growth forests where this species resides. Accurate knowledge about Xylopsora canopeorum is hindered by the challenges of accessing its canopy habitat, necessitating specialized climbing for direct observation and collection, which is strictly regulated within State and National Parks. Additionally, exploring other potential hosts within the family Cupressaceae that share similar bark characteristics to the coast redwood could provide new insights into the species' distribution and resilience strategies. [1] Previous surveys on the epiphytic lichens residing in this hard-to-access microhabitat have led to the discovery of new species. [5] [6]

Related Research Articles

<i>Psora</i> Genus of lichens

Psora is a genus of lichen-forming fungi in the family Psoraceae. Members of the genus are commonly called fishscale lichens. Lichens in the genus Psora generally have a squamulose thallus and anthraquinones in the hymenium. Photobiont partners of Psora lichens include members of the green algal genera Asterochloris, Chloroidium, Myrmecia, and Trebouxia.

<i>Sequoia sempervirens</i> Species of tree

Sequoia sempervirens is the sole living species of the genus Sequoia in the cypress family Cupressaceae. Common names include coast redwood, coastal redwood and California redwood. It is an evergreen, long-lived, monoecious tree living 1,200–2,200 years or more. This species includes the tallest living trees on Earth, reaching up to 115.9 m (380.1 ft) in height and up to 8.9 m (29 ft) in diameter at breast height. These trees are also among the longest-living organisms on Earth. Before commercial logging and clearing began by the 1850s, this massive tree occurred naturally in an estimated 810,000 ha along much of coastal California and the southwestern corner of coastal Oregon within the United States.

<i>Hypocenomyce</i> Genus of lichens

Hypocenomyce is a genus of lichen-forming fungi in the family Ophioparmaceae. Species in the genus grow on bark and on wood, especially on burned tree stumps and trunks in coniferous forest. Hypocenomyce lichens are widely distributed in the northern hemisphere.

<i>Xylopsora</i> Genus of fungi

Xylopsora is a genus of lichenized fungi, belonging to the family Umbilicariaceae.

<i>Punctelia perreticulata</i> Species of lichen

Punctelia perreticulata is a widely distributed species of foliose lichen in the family Parmeliaceae. It occurs in Mediterranean Europe and Russia, North America, South America, Australia, and New Zealand, where it grows on rocks, bark, or wood. Its main distinguishing features are its thallus surface, marked with many shallow depressions, grooves, or pits, and sorediate pseudocyphellae. The lower side of the thallus is ivory to tan towards the centre and the major secondary metabolite in the medulla is lecanoric acid. A lookalike species with which it has been historically confused is Punctelia subrudecta; this lichen can be distinguished from Punctelia perreticulata by the texture of the thallus surface, or, more reliably, by the length of its conidia.

Loxospora cristinae is a fungal species classified in 2018, found in a few European countries. It belongs to the division Ascomycota and the family Sarrameanaceae. It was first identified and described in the 19th century, but the species would not be correctly classified until almost two centuries later. Loxospora cristinae is a sterile crustose lichen, meaning it reproduces by a type of vegetative spore that has evolved specifically to produce morphological structures.

Waynea cretica is a species of corticolous (bark-dwelling), squamulose lichen in the family Ramalinaceae. It occurs on the Greek island of Crete and in Portugal.

Lecania leprosa is a species of saxicolous (rock-dwelling), crustose lichen in the family Ramalinaceae. It occurs in Eastern Europe.

Lecania sessilisoraliata is a species of saxicolous (rock-dwelling), crustose lichen in the family Ramalinaceae. It is found on rock outcrops in the mountainous Burdur region of Turkey.

<i>Psora taurensis</i> Species of lichen

Psora taurensis is a species of terricolous (ground-dwelling), squamulose lichen in the family Lecanoraceae. It is found in the Taurus Mountains of Turkey.

Biatora oxneri is a species of corticolous (bark-dwelling) lichen in the family Ramalinaceae. It is found in the Russian Far East and in South Korea.

Wilketalia is a fungal genus in the family Teloschistaceae. It is monotypic, containing the single species Wilketalia citrinoides, a saxicolous (rock-dwelling) crustose lichen found in the Bolivian Andes.

Phyllopsora amazonica is a species of corticolous (bark-dwelling), crustose lichen in the family Ramalinaceae. It is found in the Amazon rainforest of Brazil.

Phyllopsora concinna is a species of corticolous (bark-dwelling), squamulose (scaley) lichen in the family Ramalinaceae. Found in Central and South America, it was formally described as a new species in 2019 by lichenologists Sonja Kistenich and Einar Timdal. The lichen has a scaley, effuse (spread-out) thallus that is pale green with a well-developed, white prothallus. Apothecia occur rarely; they are brownish with a paler margin, measuring up to 1 mm in diameter. Ascospores are simple with a narrow ellipsoid to fusiform shape, and dimensions of 12.5–16·0 by 3.5–4.0 μm. Atranorin and parvifoliellin are major lichen products that occur in this species. The latter compound distinguishes it chemically from the morphologically similar species Phyllopsora cinchonarum, which instead contains lobaric acid. The botanical name concinna, refers to its "beautiful" appearance.

Opegrapha ramisorediata is a rare species of corticolous (bark-dwelling), crustose lichen in the family Opegraphaceae. Known to occur only in northeastern Brazil, it was described as a new species in 2017. It is characterised by a thin, pale greenish-mauve thallus.

Caloplaca sterilis is a corticolous (bark-dwelling), crustose lichen belonging to the family Teloschistaceae, described in 2011. It is primarily found in steppe and sand dune habitats in the Black Sea region, and has been recorded from Bulgaria, Romania, southwest Russia, and Ukraine. Caloplaca sterilis is characterised by tiny squamules/areoles with contrasting pale greyish-green to greenish soredia. It is easily overlooked and challenging to identify when completely sorediate and sterile, especially as its soredia do not contain the typical Sedifolia-grey pigment.

Austroplaca soropelta is a species of saxicolous and muscicolous, crustose lichen in the family Teloschistaceae. It has a bipolar distribution, meaning it occurs in polar areas of both the Northern and Southern Hemispheres.

Gallowayella galericulata is a species of corticolous and lignicolous lichen in the family Teloschistaceae. This species has small, orange, foliose (leafy), loosely adnate thalli that form either compact colonies or spread extensively. The lobes of the thallus are typically curved inward, and often form a characteristic helmet- or hood-like shape. Found in dry regions of the western United States, it colonises bark and wood, particularly favouring dry twigs of various shrubs and trees.

Rhizoplaca ouimetensis is a saxicolous (rock-dwelling), crustose lichen species in the family Lecanoraceae. Uniquely identified by its sorediate form—a feature not observed in other Rhizoplaca species—it was discovered in Ontario, Canada, specifically within the Ouimet Canyon Provincial Park.

Fulgidea is a genus of lichen-forming fungi in the family Umbilicariaceae. It has two species of squamulose lichens that grow on bark and on wood.

References

  1. 1 2 Reese Næsborg, R. (2022). "Xylopsora canopeorum". IUCN Red List of Threatened Species . 2022. Retrieved March 31, 2024.
  2. 1 2 3 4 5 6 7 8 9 10 11 12 13 Bendiksby, Mika; Næsborg, Rikke Reese; Timdal, Einar (2018). "Xylopsora canopeorum (Umbilicariaceae), a new lichen species from the canopy of Sequoia sempervirens". MycoKeys. 30 (1–15). doi: 10.3897/mycokeys.30.22271 . PMC   5804297 . PMID   29559828.
  3. "Xylopsora canopeorum Timdal, Reese Næsborg & Bendiksby". Catalogue of Life . Species 2000: Leiden, the Netherlands. Retrieved March 31, 2024.
  4. Næsborg, Rikke Reese; Peterson, Eric B.; Tibell, Leif (2019). "Chaenotheca longispora (Coniocybaceae), a new lichen from coast redwood trees in California, U.S.A." The Bryologist. 122 (1): 31–37. doi:10.1639/0007-2745-122.1.031.
  5. Williams, Cameron B.; Sillett, Stephen C. (2007). "Epiphyte communities on redwood (Sequoia sempervirens) in northwestern California". The Bryologist. 110 (3): 420–452. doi:10.1639/0007-2745(2007)110[420:ECORSS]2.0.CO;2.
  6. Williams, Cameron B.; Tibell, Leif (2008). "Calicium sequoiae, a new lichen species from north-western California, USA". The Lichenologist. 40 (3): 185–194. doi:10.1017/S0024282908007615.