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Polytrichastrum formosum

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(Redirected from Polytrichum formosum) Species of moss

Polytrichastrum formosum
Conservation status

Secure  (NatureServe)
Scientific classification Edit this classification
Kingdom: Plantae
Division: Bryophyta
Class: Polytrichopsida
Order: Polytrichales
Family: Polytrichaceae
Genus: Polytrichastrum
Species: P. formosum
Binomial name
Polytrichastrum formosum
(Hedw.) G.L. Smith

Polytrichastrum formosum, commonly known as the bank haircap moss, is a species of moss belonging to the family Polytrichaceae.

It has a cosmopolitan distribution, found mostly in temperate latitudes in the Northern Hemisphere and especially dominant in Europe and North America. However, it has also been identified in India, China, Nepal, Japan, Algeria, Australia, New Zealand, Russia, Turkey, Syria, and the Atlantic islands (i.e. Iceland).

This species was previously called Polytrichum formosum but has been reclassified as Polytrichastrum formosum due to distinct sporangial features. Recent molecular studies suggest that it should be moved back to its original genus (Polytrichum), however bryologists have not yet reached a consensus.  

Habitat

Polytrichastrum formosum generally inhabits shaded, poor soils and humus in damp coniferous forests and cool temperate rainforests. This species is most common in Europe and grows in grasslands, lowland heaths, acidic moorlands, rocky slopes, and old buildings.

Gametophyte

Like all moss, the haploid gametophyte is the dominant phase of the lifecycle of P. formosum. The moss gametophyte has photosynthetic leaves, a stem, and root-like rhizoids that anchor them to the substrate.

Polytrichastrum formosum is a medium to large robust acrocarpous moss, growing in uncrowded, unbranching tufts. Its colour ranges from green to dark olive green to greenish black. The stems of mature plants are generally 3 to 8 cm tall, however they can be as short as 2 cm or as tall as 20 cm. P. formosum, like all members of Polytrichaceae, is an endohydric moss, meaning water conduction occurs internally. This process is made possible by a central conducting strand in the stem, made up of hydroids, which are cells specialized for water transport. The stem also contains leptoids and specialized parenchyma cells that are used for conducting sugars throughout the plant. The hydrome (made of hydroids) and leptome (made of leptoids) are considered analogous in function to xylem and phloem in vascular plants. For structural support there are also thick-walled stereid cells circling the hydrome, which helps the moss grow tall.

Ventral surface of a leaf from P. formosum.

The leaves of Polytrichastrum formosum are linear-lanceolate, and are usually 6 to 8 mm in length, but can be up to 12 mm long. They are erect to spreading when the moss is dry but become broadly recurved when moist. The leaves have a toothed margin and a prominent costa, where guide cells help conduct water throughout the leaf, and stereids on the dorsal side provide protection.

Cross-section of P. formosum leaf, revealing photosynthetic lamellae.

Using a microscope, photosynthetic lamellae are visible in cross section, nearly covering the entire ventral surface of the leaf. A feature unique to Polytrichaceae, lamellae are often compared to the mesophyll of vascular plants due to their role in photosynthesis. Each lamella stands 3 to 7 cells high and the cells at the top are smooth and oblong. Lamellae help increase desiccation tolerance and photosynthetic efficiency by providing more surface area for light absorption and gas exchange. The lamellae are covered by a layer of hydrophobic wax that protects the air spaces between neighbouring lamella from being flooded with water, which would impede CO2 uptake necessary for photosynthesis. In this way, P. formosum is able withstand high irradiance better than other mosses.

Sporophyte

P. formosum angled sporophyte capsules (calyptra absent).

The diploid sporophyte generation of P. formosum matures in early summer and is short-lived. The solitary sporophyte grows out of the female gametophyte, relying on it for energy and nutrients. It is anchored to the gametophyte by a foot, and has a stalk (seta) elevating a capsule (sporangia) in which spores will develop via meiosis. The seta is yellowish to reddish brown and is 3 to 6 cm tall. Like the stem of the gametophyte, the seta has a hydrome and leptome for conducting water and sugars from the gametophyte. The slender and short-rectangular capsule is ochre to brown and 4 to 7 mm long. The capsule is terete or 4-6 angled, which distinguishes Polytrichastrum species from Polytrichum species. In the early stages of growth the capsule is covered by a hairy calyptra that protects the capsule during development and influences it's shape. At maturity, the calyptra falls off to reveal a beaked operculum. Like most other moss in Polytrichaceae, under the operculum P. formosom has 64 nematodontous peristome teeth that surround an epiphragm.

Reproduction

Sexual reproduction

Polytrichastrum formosum is sexually dioicous, meaning the male and female reproductive structures are on separate plants. P. formosum, like all members of the Polytrichaceae family, is an acrocarpous or cushion moss with reproductive structures borne at the terminus of the gametophyte stem. The perichaetial leaves surrounding the archegonia (female reproductive structure) resembles the other stem leaves besides being longer. The antheridia (male reproductive structure) are at the apex of the male gametophyte in a cup-like structure formed by perigonial leaves which are modified stem leaves. Sperm is produced in the antheridia via mitosis, and when mature they are released from the antheridia by raindrops splashing onto the cup. Sperm can be dispersed up to one meter from the male, and if they successfully reach an archegonia, the egg will be fertilized and grow into a diploid sporophyte.

Asexual reproduction

Asexual reproduction is not extensive in P. formosum, however it occurs on a local scale by the vegetative proliferation of genets.

Classification

Varieties

Taxonomy disagreement

When this species was first described by Johann Hedwig in 1801, it was classified as Polytrichum formosum. Upon further analysis it was determined by Gary L. Smith in 1971 that the moss is better described by the Polytrichastrum genus. Polytrichastrum can be distinguished from Polytrichum by sporangial features including multiple-angled capsules (more than 4 sided), elongated peristome teeth surrounding the ridged epiphragm, and larger spores. According to several sources, Polytrichastrum formosum remains the most accurate taxonomic classification. However, more recent molecular data and phylogenetic analysis suggests that P. formosum should be reverted to its original genus: Polytrichum. Their study suggested that species in Polytrichastrum and Polytrichum are in fact distantly related, but because the Polytrichastrum genus is polyphyletic, authors suggested that some species, including P. formosum, return to the Polytrichum genus. Currently, these names remain synonyms.   

References

  1. "Polytrichastrum formosum". NatureServe Explorer. NatureServe. Retrieved 2022-04-04.
  2. ^ Webmaster, David Ratz. "Bank Haircap Moss - Montana Field Guide". fieldguide.mt.gov. Retrieved 2022-04-05.
  3. ^ Flora of North America North of Mexico (2007). Bryophyta: Mosses, part 1. Vol. 27. New York: Oxford University Press. p. 130. ISBN 9780195318234.
  4. Asthana, Ashish Kumar; Vinay, Sahu; Nath, Virendra (2012). "Polytrichastrum formosum(Hedw.) G.L. Smith in India". Cryptogamie, Bryologie. 33 (1): 87–90. doi:10.7872/cryb.v33.iss1.2012.087. ISSN 1290-0796. S2CID 85607035.
  5. ^ "Polytrichastrum formosum". Atlas of British & Irish bryophytes : the distribution and habitat of mosses and liverworts in Britain and Ireland. T. L. Blockeel, Sam D. S. Bosanquet, M. O. Hill, C. D. Preston, British Bryological Society. Newbury, Berkshire. 2014. p. 418. ISBN 978-1-874357-62-9. OCLC 898120353.{{cite book}}: CS1 maint: location missing publisher (link) CS1 maint: others (link)
  6. ^ Merrill, G. L. Smith (1992). "Notes on North American Polytrichaceae: Polytrichastrum". The Bryologist. 95 (3): 270–273. doi:10.2307/3243483. ISSN 0007-2745. JSTOR 3243483.
  7. ^ Bell, Neil E.; Hyvönen, Jaakko (2010a). "A phylogenetic circumscription of Polytrichastrum (Polytrichaceae): Reassessment of sporophyte morphology supports molecular phylogeny". American Journal of Botany. 97 (4): 566–578. doi:10.3732/ajb.0900161. PMID 21622419.
  8. ^ Bell, Neil; Kariyawasam, Isuru; Flores, Jorge; Hyvönen, Jaakko (2021-06-30). "The diversity of the Polytrichopsida—a review". Bryophyte Diversity and Evolution. 43 (1). doi:10.11646/bde.43.1.8. ISSN 2381-9685. S2CID 237385196.
  9. Glime, J. M. (2017). "Meet the Bryophytes. Chapt. 2-1". Bryophyte Ecology. Volume 1. Physiological Ecology. Michigan Technological University and the International Association of Bryologists.
  10. ^ Glime, J.M. (2017). "Water Relations: Conducting Structures. Chapt. 7-1". Bryophyte Ecology. Volume 1. Physiological Ecology. Michigan Technological University and the International Association of Bryologists.
  11. ^ Glime, J.M. (2017). "Bryophyta - Andreaeopsida, Andreaeobryopsida, Polytrichopsida. Chapt. 2-6.". Bryophyte Ecology. Volume 1. Physiological Ecology. Michigan Technological University and the International Association of Bryologists.
  12. ^ PRESSEL, SILVIA; LIGRONE, ROBERTO; DUCKETT, JEFFREY G. (2006). "Effects of De- and Rehydration on Food-conducting Cells in the Moss Polytrichum formosum: A Cytological Study". Annals of Botany. 98 (1): 67–76. doi:10.1093/aob/mcl092. ISSN 0305-7364. PMC 2803544. PMID 16735407.
  13. ^ Proctor, Michael C. F.; Ligrone, Roberto; Duckett, Jeffrey G. (2007-01-01). "Desiccation Tolerance in the Moss Polytrichum formosum: Physiological and Fine-structural Changes during Desiccation and Recovery". Annals of Botany. 99 (1): 75–93. doi:10.1093/aob/mcl246. ISSN 0305-7364. PMC 2802982. PMID 17158142.
  14. ^ Thomas, Robert J.; Ryder, Steve H.; Gardner, Mark I.; Sheetz, Jonathan P.; Nichipor, Stephen D. (1996). "Photosynthetic Function of Leaf Lamellae in Polytrichum commune". The Bryologist. 99 (1): 6–11. doi:10.2307/3244431. ISSN 0007-2745. JSTOR 3244431.
  15. Proctor, M. C. F. (2005). "Why do Polytrichaceae have lamellae?". Journal of Bryology. 27 (3): 221–229. Bibcode:2005JBryo..27..221P. doi:10.1179/174328205X69968. ISSN 0373-6687. S2CID 84580845.
  16. Clayton-Greene, K. A.; Collins, N. J.; Green, T. G. A.; Proctor, M. C. F. (1985-01-01). "Surface wax, structure and function in leaves of Polytrichaceae". Journal of Bryology. 13 (4): 549–562. Bibcode:1985JBryo..13..549C. doi:10.1179/jbr.1985.13.4.549. ISSN 0373-6687.
  17. ^ Glime, J. M. (2017). "Ecophysiology of Development: Sporophyte. Chapt. 5-9.". Bryophyte Ecology. Volume 1. Physiological Ecology. Michigan Technological University and the International Association of Bryologists.
  18. Van der Velde, M.; During, H. J.; Van de Zande, L.; Bijlsma, R. (2001-12-21). "The reproductive biology of Polytrichum formosum: clonal structure and paternity revealed by microsatellites: REPRODUCTIVE BIOLOGY OF POLYTRICHUM FORMOSUM". Molecular Ecology. 10 (10): 2423–2434. doi:10.1046/j.0962-1083.2001.01385.x. PMID 11742546. S2CID 19716812.
  19. ^ Smith, Gary L. (1971). "A conspectus of the genera of Polytrichaceae". Mem. New York Bot. Gard. 21 (3): 1–83. ISBN 978-0893270728.
  20. "ITIS - Report: Polytrichastrum formosum". www.itis.gov. Retrieved 2022-04-13.
Taxon identifiers
Polytrichastrum formosum
Polytrichum formosum
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