Cladonia rangiferina explained

Cladonia rangiferina, also known as reindeer cup lichen, reindeer lichen (cf. Sw. renlav) or grey reindeer lichen, is a light-coloured fruticose, cup lichen species in the family Cladoniaceae. It grows in both hot and cold climates in well-drained, open environments. Found primarily in areas of alpine tundra, it is extremely cold-hardy.

Other common names include reindeer moss, deer moss, and caribou moss, but these names can be misleading since it is, though somewhat moss-like in appearance, not a moss. As the common names suggest, reindeer lichen is an important food for reindeer (caribou), and has economic importance as a result. Synonyms include Cladina rangiferina and Lichen rangiferinus.

Taxonomy

Cladonia rangiferina was first scientifically described by Carl Linnaeus in his 1753 Species Plantarum; as was the custom at the time, he classified it in the eponymous genus, as Lichen rangiferinus. Friedrich Heinrich Wiggers transferred it to the genus Cladonia in 1780.

Description

Thalli are fruticose, and extensively branched, with each branch usually dividing into three or four (sometimes two); the thicker branches are typically NaNmm in diameter. The colour is greyish, whitish or brownish grey. C. rangiferina forms extensive mats up to 10cm (00inches) tall. The branching is at a smaller angle than that of Cladonia portentosa. It lacks a well-defined cortex (a protective layer covering the thallus, analogous to the epidermis in plants), but rather, a loose layer of hyphae cover the photobionts. The photobiont associated with the reindeer lichen is Trebouxia irregularis.It grows on humus, or on soil over rock. It is mainly found in the taiga and the tundra.

Reindeer lichen, like many lichens, is slow growing (NaNdisp=orNaNdisp=or per year) and may take decades to return once overgrazed, burned, trampled, or otherwise damaged.[1]

A similar-looking but distinct species, also known by the common name "reindeer lichen", is Cladonia portentosa.

Chemistry

A variety of bioactive compounds have been isolated and identified from C. rangiferina, including abietane, labdane, isopimarane, the abietane diterpenoids hanagokenols A and B, obtuanhydride, sugiol, 5,6-dehydrosugiol, montbretol, cis-communic acid, imbricatolic acid, 15-acetylimbricatoloic acid, junicedric acid, 7α-hydroxysandaracopimaric acid, β-resorylic acid, atronol, barbatic acid, homosekikaic acid, didymic acid and condidymic acid. Some of these compounds have mild inhibitory activities against methicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococci.Exposure to UV-B radiation induces the accumulation of usnic acid and melanic compounds. Usnic acid is thought to play a role in protecting the photosymbiont by absorbing excess UV-B.

Resynthesis

Resynthesis experiments have been conducted to study the early stages of lichen formation in Cladonia rangiferina. These experiments involve isolating and culturing the fungal and algal partners separately, then reuniting them under laboratory conditions to observe the process of lichenization. Through these studies, researchers have identified several key stages in the early development of the lichen thallus.

The first stage, known as the pre-contact stage, occurs around one day post co-inoculation. During this stage, no apparent fungal or algal growth is observed, and hyphal tips are not growing towards algal cells. By the eighth day post co-inoculation, the contact stage is reached. This stage is characterised by rich branching of fungal hyphae with short internodes. Hyphal tips grow towards algal cells, and some form swollen tips called appressoria upon contact. Hyphae can be observed growing around single algal cells or clusters, and mucilage is frequently present. The growth together stage is typically observed around 21 days post co-inoculation. At this point, coordinated growth between the fungus and alga becomes evident. Algal cells are integrated within a hyphal matrix, with hyphae emerging through algal colonies and forming networks within and between them.

Quantitative measurements during these stages reveal several patterns. In compatible interactions, researchers observe significantly shorter hyphal internode lengths and more lateral branches compared to incompatible ones. The frequency of appressoria formation increases over time in compatible interactions. There is no significant reduction in algal cell diameter in compatible interactions, unlike in some incompatible pairings. These experiments highlight the specificity of the Cladonia rangiferinaAsterochloris glomerata/irregularis symbiosis. When paired with incompatible algae such as Coccomyxa peltigerae or Chloroidium ellipsoideum, C. rangiferina shows reduced growth and fewer symbiosis-specific morphological changes.

The resynthesis process in C. rangiferina appears to be slower compared to some other lichen species. Researchers have not observed a well-organised prethallus stage even after three months of co-cultivation. This may be due to specific environmental requirements or growth conditions needed for complete thallus formation in this species. These studies provide insights into the recognition mechanisms and early developmental processes involved in lichen formation. The observations support the concept of controlled parasitism in lichen symbiosis, where the fungal partner exhibits parasitic behavior, but in a controlled manner that allows for mutual benefit in the long term.

Habitat

Cladonia rangiferina often dominates the ground in boreal pine forests and open, low-alpine sites in a wide range of habitats, from humid, open forests, rocks and heaths. A specific biome in which this lichen is represented is the boreal forests of Canada.[2]

Ecology

Cladonia rangiferina is a known host to the lichenicolous fungus species Lichenopeltella rangiferinae, which is named after C. rangiferina, Lichenoconium pyxidatae and Lichenopeltella uncialicola

Conservation

In certain parts of its range, this lichen is an endangered species. For example, in the British Duchy of Cornwall it is protected under the UK Biodiversity Action Plan.

Uses

The reindeer lichen is edible, but crunchy. It can be soaked with wood ashes to remove its bitterness, then added to milk or other dishes.[3] It is a source of vitamin D.[4]

This lichen can be used in the making of aquavit,[5] and is sometimes used as decoration in glass windows. The lichen is used as a traditional remedy for removal of kidney stones by the Monpa in the alpine regions of the West Kameng district of Eastern Himalaya. The Inland Dena'ina used reindeer lichen for food by crushing the dry lichen and then boiling it or soaking it in hot water until it becomes soft. They eat it plain or, preferably, mixed with berries, fish eggs, or lard. The Inland Dena'ina also boil reindeer lichen and drink the juice as a medicine for diarrhea. Acids present in lichens mean their consumption may cause an upset stomach, especially if not well cooked.[6]

According to a study published in 2017, reindeer lichen was able to grow on burnt soil as soon as two years after a forest fire in Northern Sweden, indicating that artificial replanting of lichen could be a useful strategy for the restoration of reindeer pastures.

See also

Notes and References

  1. Web site: Rook EJS . 11 October 1999 . Cladonia species. Reindeer lichens . 2012-03-25 . 2012-04-03 . https://web.archive.org/web/20120403233709/http://www.rook.org/earl/bwca/nature/moss/cladonia.html . dead .
  2. C. Michael Hogan. 2008. Black Spruce: Picea mariana, GlobalTwitcher.com, ed. N. Stromberg
  3. Book: The Complete Guide to Edible Wild Plants . . . 2009 . 978-1-60239-692-0 . New York . 85 . en-US . 277203364.
  4. Björn . L.O. . Wang . T. . 2000 . Vitamin D in an ecological context . International Journal of Circumpolar Health . 59 . 1 . 26–32 . 1239-9736 . 10850004.
  5. Book: Meuninck, Jim . Basic Illustrated Edible Wild Plants and Useful Herbs . 2018 . Falcon Guides . 978-1-4930-3641-7 . 14.
  6. Web site: Caribou Moss – Cladonia rangiferina . 2009-01-12.