Eastern Wood Pewee

by | Feb 25, 2018 | Pewee

How Can We Help?
You are here:
< Back

Parmelia sulcata is a foliose lichen in the family Parmeliaceae. It is very tolerant of pollution and has a cosmopolitan distribution, making it one of the most common lichens. It harbours a unicellular Trebouxia green algal symbiont.

Systematics

Historical taxonomy

Parmelia sulcata was first described by Thomas Taylor in 1836 under its current name. Taylor characterized its thallus as orbicular and stellate, with a glaucous (dull grayish-green) white color when dry and a glaucous green color when wet, and a dark brown underside with black fibers. He described the lobes as incised, somewhat concave, and reticulated with elevated ridges. The thallus features oblong or linear eruptions consisting of a fine greyish-brown powder. Apothecia are central and substipitate, with a brown disk and a smooth or powdery exterior. Taylor noted that Parmelia sulcata was distinct from Parmelia saxatilis, being larger, whiter, less imbricated, more concave, and more green when wet. He also highlighted that the species is more common on rocks in County Kerry than on trees and could attain a diameter of a foot or more. Taylor mentioned that it had been previously mistaken for Parmelia conspersa (now in Xanthoparmelia) in some plant lists.[2] Parmelia sulcata has a large number of named varieties and forms, but no subspecies despite its extensive range. Most taxonomists have left the species in the genus to which Taylor originally assigned it, though mycologist Maurice Choisy assigned it to the genus Parmotrema in 1952.[3]

In 1962, Mason Hale and Syo Kurokawa designated a specimen from Lough Bray, County Kerry, as the lectotype for Parmelia sulcata. This specimen, collected by Taylor in 1812 and housed in the Farlow Herbarium of Cryptogamic Botany, was supported by Taylor's own notes, confirming its identification. Despite attempts to extract DNA from the original lectotype, no viable DNA was obtained, leading to the selection of an epitype from a specimen collected near the original type locality in County Kerry in 2006. This epitype helps stabilize the application of the name Parmelia sulcata in both molecular and morphological studies.[4]

Molecular studies

Molecular phylogenetics studies revealed significant genetic variability within Parmelia sulcata, indicating that it is a complex of cryptic species. Molina and colleagues (2011) used three molecular markers (nuITS, nuIGS rDNA, and partial β-tubulin gene) to study the biodiversity of P. sulcata across four continents. They identified two monophyletic groups: Parmelia sulcata sensu stricto ("in the strict sense") and a new cryptic species named Parmelia encryptata. The study highlighted that P. sulcata as traditionally circumscribed did not form a monophyletic group. The researchers found that specimens initially identified as P. sulcata based on morphological characters did not cluster together in phylogenetic analyses. Instead, they formed distinct, well-supported clades, indicating the presence of multiple cryptic species within what was previously thought to be a single species. P. encryptata was described as morphologically similar to P. sulcata but genetically distinct, with a unique insertion in the internal transcribed spacer region and specific nucleotide differences.[4] Another member of this complex, the widely distributed Parmelia barrenoae, was recognized as a distinct species in 2005.[5]

Naming

The genus name Parmelia is a compound of two Greek words: parme, meaning "fruit bowl" and -eileo, meaning "enclosed". This likely refers to the lecanorine apothecia of species belonging to the genus.[6] The specific epithet sulcata is derived from sulcatus, meaning "grooved" or "furrowed".[7] The species is known by a number of colloquial names, including hammered shield lichen,[8] cracked-shield lichen,[9] powdered crottle,[10] furrowed shield lichen, powdered shield, and waxpaper lichen.[11]

Description

Closeup of lobe with both laminal and marginal soralia

Parmelia sulcata is a foliose lichen with a generally circular thallus that can range in color from glaucous white to gray on the upper cortex; the lower surface is black. The thallus is broadly lobed.[12] The thallus, loosely attached to its substrate, is typically up to 6 cm (2.4 in), although diameters up to 10 cm (3.9 in) have been recorded.[13] Each lobe measures between 2–5 mm (0.08–0.20 in) in width,[8] and lobes are overlapping.[12] The lobes, which are more or less linear, have both marginal and laminal soralia.[14] Also present on both laminal and marginal regions of the lobes are elongated pseudocyphellae—small pores in the cortex—that form a reticulate pattern.[15] Rhizines on the thallus underside are simple (unbranched) to squarrose (brush-like).[14] Apothecia (fruiting bodies) are rare in this species.[13] If present, they are up to 8 mm (5⁄16 in) in diameter and lecanorine in form, with a red-brown disc; they often have a sorediate margin. Ascospores measure 8–14 μm.[15]

In terms of standard spot tests, the upper surface of Parmelia sulcata reacts K+ (yellow), KC−, C−, and P−, indicating the presence of the secondary metabolites (lichen products) atranorin and chloroatranorin.[15] The lichen's medulla and soredia are K+ (red-orange) and Pd+ (orange). The lichen does not fluoresce in ultraviolet light.[12] Salazinic acid and consalazinic acid are present in the medulla; lobaric acid is variably present.[15]

Photobiont

The photobiont, or photosynthetic partner, of Parmelia sulcata is primarily the green microalga Trebouxia. A 2021 study by Moya and colleagues shed light on the diversity and specificity of Trebouxia species associated with P. sulcata. Trebouxia is one of the most frequent lichen symbionts, associating with over 7,000 species of lichen-forming fungi worldwide. The study analyzed 159 thalli from 30 locations, including samples of P. sulcata. It was found that P. sulcata is highly specific to Trebouxia clade I, interacting with three specific Trebouxia species: Trebouxia sp. I02, T. flava, and Trebouxia aff. flava. This specificity suggests a close co-evolutionary relationship between Parmelia sulcata and its photobiont.[16]

Phylogenetic analyses revealed that while some Parmelia species can associate with multiple Trebouxia species, P. sulcata maintains a more specialized relationship with fewer Trebouxia lineages. This high specificity could be related to the lichen's ecological strategies and vegetative structures. Parmelia sulcata reproduces vegetatively through soredia, which contain both fungal and algal cells, potentially influencing the selection of compatible photobionts. Overall, the study suggests that the biodiversity patterns of photobionts in Parmelia are influenced by a combination of ecological, climatic, and evolutionary factors.[16]

Similar species

Parmelia barrenoae is one of several potential lookalikes of P. sulcata.

Parmelia sulcata has several morphologically and chemically similar species that can be challenging to distinguish without detailed examination and molecular data. These species include Parmelia barrenoae, Parmelia encryptata, and Parmelia asiatica. Identifying Parmelia sulcata and its similar species based solely on morphology and chemistry can be challenging due to overlapping characteristics and intraspecific variability. DNA-based methods are essential tools to help distinguish between cryptic species like P. encryptata and near-cryptic species such as P. asiatica and P. barrenoae. Understanding these differences enables researchers and lichenologists to better identify and study Parmelia sulcata and its closely related species, contributing to more accurate distribution records and ecological knowledge.[14]

Parmelia barrenoae can be distinguished by its broad and overlapping lobes. The soralia are laminal, appearing as fissures in the upper cortex. The rhizines of P. barrenoae are simple to furcate. While both P. barrenoae and P. sulcata contain salazinic acid, the physical arrangement and appearance of lobes and soralia are distinguishing features.[14]

Parmelia encryptata is a cryptic species that is morphologically identical to P. sulcata. It is characterized by sublinear lobes with marginal and laminal, elongated pseudocyphellae, and soralia on the upper surface. The rhizines are typically simple to squarrose, predominantly simple in the central part of the thallus. Identification of P. encryptata requires molecular data, specifically nucITS rDNA sequences, to distinguish it from P. sulcata.[14]

Parmelia asiatica is distinguished by its predominantly circular and semicircular, terminal, or marginal soralia, and narrow sublinear lobes. Like P. sulcata, P. asiatica has simple to squarrose rhizines but differs in the shape and distribution of its soralia. Both species have salazinic acid in the medulla, but the unique characteristics of P. asiatica's soralia and lobes provide a visual distinction.[14]

Distribution and habitat

Parmelia sulcata is a common species throughout much of the world, found from temperate to cold regions of both the Northern and Southern Hemispheres.[17] It is one of the most common parmelioid lichens in Europe,[4] having been recorded in 43 countries there.[18][19] It has been found to reappear in urban areas after sulphur dioxide levels have decreased.[20][21] Although common in the Northern Hemisphere, Parmelia sulcata is rare in South America. A 2023 study provided molecular evidence for its presence in Chile, and showed that DNA sequences from Chile belong to the most common haplotype found in Europe, Asia, and North America, indicating a widespread distribution of this haplotype.[14]

Although most common on bark and on wood, Parmelia sulcata also grows on rocks or mossy rocks.[13] In a study of the distribution of epiphytic lichens, including Parmelia sulcata, along tree trunks in a temperate continental climate, it was found to be most abundant in the middle to upper parts of tree trunks, particularly in areas with higher light levels. This distribution pattern suggests that light conditions are a significant factor influencing the growth and distribution of Parmelia sulcata.[22]

Ecology

In the Tatra Mountains, Poland

The vertical zonality of Parmelia sulcata along tree trunks is influenced by various microclimatic conditions such as humidity, light conditions, and the chemical and physical properties of the bark. Parmelia sulcata, along with other lichen species, contributes to the high diversity of lichen biota in the lower and upper parts of tree trunks. The species composition of lichens, including Parmelia sulcata, changes from the base to the crown of the trees, indicating the importance of light conditions in their distribution. For instance, in a Russian study, Parmelia sulcata was commonly found at heights of 10–20 m (33–66 ft) on birch trees and around 15 m (49 ft) and in the crown on spruce trees, reflecting its preference for higher insolation levels (i.e., areas that receive more sunlight or solar radiation) in these zones.[22]

A study conducted in a temperate deciduous forest of Central Italy monitored carbon dioxide (CO2) gas exchange, radial growth, chlorophyll content, and photobiont density of Parmelia sulcata over a year. The results showed significant seasonal variations, with CO2 gas exchange and radial growth peaking in December, and photoinhibition occurring in early spring before tree leaves sprouted. Photobiont density was highest in June and December and lowest in April. These findings suggest that the seasonal acclimation of lichen photosynthesis and chlorophyll content is influenced by variations in photobiont population density, potentially related to changes in nutrient availability.[23]

Parmelia sulcata often grows in lichen communities with other species. In the Jura Mountains of Switzerland, for example, it regularly occurs with Lobaria pulmonaria and various Nephroma species.[24]

Lichenoconium edgewoodensis and Nanostictis caucasica are two species of lichenicolous (lichen-dwelling) fungi that have been recorded exclusively parasitizing Parmelia barrenoae, although it is also susceptible to other species of parasitic fungi that more broadly target genus Parmelia, such as Arthophacopsis parmeliarum or Abrothallus parmeliarum.[25] Another fungus that appears to be obligately parasitic on P. sulcata, Perigrapha superveniens, causes the formation of irregularly shaped to undulate (wavy edged) galls, and prefers its host to live in oceanic areas.[26]

Uses

This species can be used to make dyes, producing a reddish-brown color.[27] Indigenous people in North America used the lichen medicinally. The Métis peoples rubbed it on the gums of teething babies, while the Saanich peoples used it for a variety of ailments, with the medicinal qualities depending on what type of tree it was harvested from.[28]

Environmental monitoring

Parmelia sulcata has been extensively studied for its capacity to monitor environmental pollution due to its sensitivity to air quality changes. It has been used to monitor pollutants, such as heavy metals, in various environments including industrial areas, urban settings, and natural habitats. Studies have shown that the lichen can accumulate pollutants, reflecting the levels of pollutants in the air. For instance, P. sulcata was used in European air pollution-biomonitoring programs to monitor persistent polycyclic aromatic hydrocarbon pollution in the Pyrenees. It was also used to assess metal pollutants in industrial areas of the Iberian Peninsula and to monitor air quality in the Apostle Islands (Wisconsin, USA) and Pretoria (South Africa). Additionally, the lichen's ability to survive in radionuclide-polluted environments allows researchers to quantify levels of radioactive pollutants by analyzing the concentrations of radionuclides accumulated in the lichen's tissues.[29]

Research

Parmelia sulcata has been studied for its antimicrobial and cytotoxic properties. Various extracts, including acetone, methanol, and aqueous extracts, have shown antimicrobial activity against a range of bacterial and fungal species. The presence of salazinic acid is attributed to its antimicrobial effects. Additionally, P. sulcata has demonstrated cytotoxic properties against several cancer cell lines. Studies have shown its effectiveness in inducing caspase-independent apoptotic cell death in breast cancer cell lines and DNA damage-induced apoptosis in lung and liver cancer cells.[29]

References

  1. ^ "Synonymy: Parmelia sulcata Taylor, in Mackay, Fl. Hibern. 2: 145 (1836)". Species Fungorum. Retrieved 19 June 2024.
  2. ^ Mackay, J.T. (1836). Flora Hibernica. Vol. 2. Dublin: Willam Curry Jun and Company. p. 145.
  3. ^ "Parmelia sulcata". MycoBank. Retrieved 7 April 2018.
  4. ^ a b c Molina, Maria del Carmen; Divakar, Pradeep K.; Millanes, Ana M.; Sánchez, Edinson; Del-Prado, Ruth; Hawksworth, David L.; Crespo, Ana (2011). "Parmelia sulcata (Ascomycota: Parmeliaceae), a sympatric monophyletic species complex". The Lichenologist. 43 (6): 585–601. doi:10.1017/S0024282911000521.
  5. ^ Divakar, Pradeep K.; Molina, M. Carmen; Lumbsch, H. Thorsten; Crespo, Ana (2005). "Parmelia barrenoae, a new lichen species related to Parmelia sulcata (Parmeliaceae) based on molecular and morphological data". The Lichenologist. 37 (1): 37–46. doi:10.1017/s0024282904014641.
  6. ^ Hinds, James W. "Lichen Flora of Eastern North America: The Genus Parmelia Sensu Stricto". New York Botanical Garden. Retrieved 7 April 2018.
  7. ^ Stearn, William Thomas (1992). Botanical Latin: History, Grammar, Syntax, Terminology and Vocabulary. Newton Abbot, UK: David & Charles. p. 491. ISBN 978-0-7153-9901-9.
  8. ^ a b Brodo, Irwin W.; Sharnoff, Sylvia Duran; Sharnoff, Stephen (2001). Lichens of North America. New Haven, CT, USA: Yale University Press. p. 484. ISBN 978-0-300-08249-4.
  9. ^ Houck, Michael C.; Cody, Mary Jane (2000). Wild in the City: A Guide to Portland's Natural Areas. Portland, OR, US: Oregon Historical Society Press. p. 249. ISBN 978-0-87595-273-4.
  10. ^ "Lichens of Welsh Atlantic Woodlands" (PDF). plantlife.org. Plantlife International. Retrieved 25 May 2018.
  11. ^ Qian, Hong; Klinka, Karel (1998). Plants of British Columbia: Scientific and Common Names of Vascular Plants, Bryophytes and Lichens. Vancouver, Canada: UBC Press. pp. 485, 504, 520. ISBN 978-0-7748-0652-7.
  12. ^ a b c Dobson, Frank S. (2011). Lichens: An Illustrated Guide to the British and Irish Species. Slough, UK: Richmond Publishing. p. 305. ISBN 978-0-85546-315-1.
  13. ^ a b c McCune, Bruce; Geiser, Linda (2023). Macrolichens of the Pacific Northwest (3 ed.). Corvallis: Oregon State University Press. p. 278. ISBN 978-0-87071-251-7.
  14. ^ a b c d e f g Ossowska, Emilia Anna; Schiefelbein, Ulf; Szymczyk, Rafał; Kukwa, Martin (2023). "Contribution to the knowledge of the distribution of Parmelia species (Parmeliaceae, Ascomycota) – New records confirmed by molecular data". Acta Mycologica. 58: 1–11. doi:10.5586/am/175356.
  15. ^ a b c d McMullin, R. Troy (2023). Lichens. The Macrolichens of Ontario and the Great Lakes Region of the United States. Firefly Books. p. 321. ISBN 978-0-228-10369-1.
  16. ^ a b Moya, Patricia; Molins, Arantzazu; Škaloud, Pavel; Divakar, Pradeep K.; Chiva, Salvador; Dumitru, Cristina; Molina, Maria Carmen; Crespo, Ana; Barreno, Eva (2021). "Biodiversity Patterns and ecological preferences of the photobionts associated with the lichen-forming genus Parmelia". Frontiers in microbiology. 12: 1–14. doi:10.3389/fmicb.2021.765310. PMC 8739953. PMID 35003003.
  17. ^ Amo de Paz, Guillermo; Cubas, Paloma; Divakar, Pradeep K.; Lumbsch, H. Thorsten; Crespo, Ana (December 2011). "Origin and Diversification of Major Clades in Parmelioid Lichens (Parmeliaceae, Ascomycota) during the Paleogene Inferred by Bayesian Analysis". PLOS ONE. 6 (12): e28161. Bibcode:2011PLoSO...628161A. doi:10.1371/journal.pone.0028161. PMC 3234259. PMID 22174775.
  18. ^ Hawksworth, David L.; Blanco, Oscar; Divakar, Pradeep K.; Ahti, Teuvo; Crespo, Ana (2008). "A first checklist of parmelioid and similar lichens in Europe and some adjacent territories, adopting revised generic circumscriptions and with indications of species distributions". The Lichenologist. 40 (1): 1–21. doi:10.1017/S0024282908007329.
  19. ^ Hawksworth, David L.; Divakar, Pradeep K.; Crespo, Ana; Ahti, Teuvo (2011). "The checklist of parmelioid and similar lichens in Europe and some adjacent territories: Additions and corrections". The Lichenologist. 43 (6): 639–645. doi:10.1017/S0024282911000454.
  20. ^ Hawksworth, David L.; McManus, Paulette M. (1989). "Lichen recolonization in London under conditions of rapidly falling sulphur dioxide levels, and the concept of zone skipping". Botanical Journal of the Linnean Society. 100 (2): 99–109. doi:10.1111/j.1095-8339.1989.tb01712.x.
  21. ^ Crespo, Ana; Divakar, Pradeep K.; Argüello, Arturo; Gasca, Concepción; Hawksworth, David L. (2004). "Molecular studies on Punctelia species of the Iberian Peninsula, with an emphasis on specimens newly colonizing Madrid". The Lichenologist. 36 (5): 299–308. doi:10.1017/S0024282904014434.
  22. ^ a b Muchnik, E.E.; Blagoveschenskaya, E. Yu. (2022). "Distribution of epiphytic lichens along a tree's trunk". Russian Journal of Ecology. 53 (6): 448–455.
  23. ^ Tretiach, Mauro; Bertuzzi, Stefano; Candotto Carniel, Fabio; Virgilio, Damiano (2013). "Seasonal acclimation in the epiphytic lichen Parmelia sulcata is influenced by change in photobiont population density". Oecologia. 173 (3): 649–663. doi:10.1007/s00442-013-2654-3.
  24. ^ Werth, S.; Wagner, H. H.; Gugerli, F.; Holderegger, R.; Csencsics, D.; Kalwij, J. M.; Scheidegger, C. (April 2006). "Epiphytic Lichen". Bulletin of the Ecological Society of America. 87 (2): 105. doi:10.1890/0012-9623(2006)87[105:el]2.0.co;2. JSTOR bullecosociamer.87.2.10.
  25. ^ Diederich, Paul; Lawrey, James D.; Ertz, Damien (2018). "The 2018 classification and checklist of lichenicolous fungi, with 2000 non-lichenized, obligately lichenicolous taxa". The Bryologist. 121 (3): 340–425. doi:10.1639/0007-2745-121.3.340.
  26. ^ Holien, Håkon; Frisch, Andreas (2022). "Perigrapha superveniens (Nyl.) Hafellner, a lichenicolous fungus new to Fennoscandia from Norway" (PDF). Graphis Scripta. 34 (3): 36–41.Open access icon
  27. ^ Casselman, Karen Diadick (2001). Lichen Dyes: The New Source Book. Mineola, NY, US: Dover Publications. p. 35. ISBN 978-0-486-41231-3.
  28. ^ Ranković, Branislav, ed. (2015). Lichen Secondary Metabolites: Bioactive Properties and Pharmaceutical Potential. Switzerland: Springer Publishing. p. 49. ISBN 978-3-319-13373-7.
  29. ^ a b González-Burgos, Elena; Fernández-Moriano, Carlos; Gómez-Serranillos, M. Pilar (2019). "Current knowledge on Parmelia genus: Ecological interest, phytochemistry, biological activities and therapeutic potential". Phytochemistry. 165: 1–14. doi:10.1016/j.phytochem.2019.112051.
Categories
Table of Contents