Thelephora terrestris

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Thelephora terrestris
Thelephora.terrestris.-.lindsey.jpg
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Fungi
Division: Basidiomycota
Class: Agaricomycetes
Order: Thelephorales
Family: Thelephoraceae
Genus: Thelephora
Species:
T. terrestris
Binomial name
Thelephora terrestris
Ehrh. (1787)

Thelephora terrestris, commonly known as the common fiber vase [1] or earthfan fungus [2] is an inedible species of fungus in the Basidiomycota phylum. [3]

Contents

History and taxonomy

This fungus was first described by Jakob Friedrich Ehrhart in 1787. [4] [5]

Habitat and ecology

Throughout North America [1] and Europe [5] Thelephora terrestris can be found in soil. It is commonly found in sandy soils under pine trees, on roots [1] and twigs. [6]

This ectomycorrhizal fungus forms a symbiotic relationship known as mycorrhizae, especially with Pinus species. [7] It is commonly found in pine forests [8] as well as plant nursery soils world wide. [9] This fungus is known to get water and nutrients from far away [10] and being capable of growing in both low fertility and high fertility soils. [2]

It is a dominant mycorrhizal fungus, [9] re-establishes quickly after disturbances such as forest fire, and is considered stress tolerant. [11]

Outside of the Pinus genus, it is also capable of forming mycorrizha with other trees such as alder, birch, oak, beech, and poplar. [2]

Thelephora terrestris virus 1 (TtV1), which is a mycovirus, can infect this fungus. [2]

Description

Thelephora terrestris is present year round, though is mostly seen July to December. [1] As the fruiting body forms, it starts off lighter in colour then turns to a darker shade of brown as it ages. [7] A stalk may not be present, if there is one, it is usually very short. [1] Sometimes the fungus is grown in large colonies. [6] The shape is described as a fan and can grow up to 6 cm wide. [6] It has been described to have a moldy earth like smell. [1]

Thelephora terrestris
Information icon.svg
Smooth icon.pngSmooth hymenium
No cap icon.svgNo distinct cap
NA cap icon.svg Hymenium attachment is not applicable
Bare stipe icon.svg Stipe is bare
Transparent spore print icon.svg
Spore print is purple-brown
Mycorrhizal fungus.svgEcology is mycorrhizal
Mycomorphbox Inedible.pngEdibility is inedible

The hyphae of mycorrhizal forms walls that becomes thicker as it ages, while in earlier stages may be spiney. [12] When mating, the hyphae forms clamp connections [7] The spores are purple-brown colour, [1] ellipsoid or angular shape. [6]

The edibility of this fungus is unknown, but it is considered too tough to be worthwhile. [13]

Thelephora palmata is a similar species which is comparatively stinky and less widely distributed. [13] [14]

Physiology

The full life cycle can be reproduced and studied in a laboratory, both ectomycorrhizal form and mushroom form. [15]

Due to the mycotoxins that the fungi produces, it protects pinus trees from root pathogen Phytophthora cinnamomi . [9]

Related Research Articles

<span class="mw-page-title-main">Mycorrhiza</span> Fungus-plant symbiotic association

A mycorrhiza is a symbiotic association between a fungus and a plant. The term mycorrhiza refers to the role of the fungus in the plant's rhizosphere, its root system. Mycorrhizae play important roles in plant nutrition, soil biology, and soil chemistry.

<span class="mw-page-title-main">Truffle</span> Fruiting body of a subterranean ascomycete fungus

A truffle is the fruiting body of a subterranean ascomycete fungus, one of the species of the genus Tuber. More than one hundred other genera of fungi are classified as truffles including Geopora, Peziza, Choiromyces, and Leucangium. These genera belong to the class Pezizomycetes and the Pezizales order. Several truffle-like basidiomycetes are excluded from Pezizales, including Rhizopogon and Glomus. Truffles are ectomycorrhizal fungi, so they are found in close association with tree roots. Spore dispersal is accomplished through fungivores, animals that eat fungi. These fungi have ecological roles in nutrient cycling and drought tolerance.

<i>Suillus luteus</i> Species of edible fungus in the family Suillaceae native to Eurasia

Suillus luteus is a bolete fungus, and the type species of the genus Suillus. A common fungus native all across Eurasia from Ireland to Korea, it has been introduced widely elsewhere, including North and South America, southern Africa, Australia and New Zealand. Commonly referred to as slippery jack or sticky bun in English-speaking countries, its names refer to the brown cap, which is characteristically slimy in wet conditions. The fungus, initially described as Boletus luteus by Carl Linnaeus in 1753, is now classified in a different fungus family as well as genus. Suillus luteus is edible, though not as highly regarded as other bolete mushrooms. It is commonly prepared and eaten in soups, stews or fried dishes. The slime coating, however, may cause indigestion if not removed before eating. It is often sold as a dried mushroom.

<i>Laccaria bicolor</i> Species of fungus

Laccaria bicolor is a small tan-colored mushroom with lilac gills. It is edible but not choice, and grows in mixed birch and pine woods. It is found in the temperate zones of the globe, in late summer and autumn. L. bicolor is an ectomycorrhizal fungus used as a soil inoculant in agriculture and horticulture.

<i>Rhizopogon</i> Genus of fungi

Rhizopogon is a genus of ectomycorrhizal basidiomycetes in the family Rhizopogonaceae. Species form hypogeous sporocarps commonly referred to as "false truffles". The general morphological characters of Rhizopogon sporocarps are a simplex or duplex peridium surrounding a loculate gleba that lacks a columnella. Basidiospores are produced upon basidia that are borne within the fungal hymenium that coats the interior surface of gleba locules. The peridium is often adorned with thick mycelial cords, also known as rhizomorphs, that attach the sporocarp to the surrounding substrate. The scientific name Rhizopogon is Greek for 'root' (Rhiz-) 'beard' (-pogon) and this name was given in reference to the rhizomorphs found on sporocarps of many species.

<span class="mw-page-title-main">Hydnellum peckii</span> Species of fungus

Hydnellum peckii is a fungus in the genus Hydnellum of the family Bankeraceae. It is a hydnoid species, producing spores on the surface of vertical spines or tooth-like projections that hang from the undersurface of the fruit bodies. It is found in North America, Europe, and was recently discovered in Iran (2008) and Korea (2010). Hydnellum peckii is a mycorrhizal species, and forms mutually beneficial relationships with a variety of coniferous trees, growing on the ground singly, scattered, or in fused masses.

Microbial inoculants, also known as soil inoculants or bioinoculants, are agricultural amendments that use beneficial rhizosphericic or endophytic microbes to promote plant health. Many of the microbes involved form symbiotic relationships with the target crops where both parties benefit (mutualism). While microbial inoculants are applied to improve plant nutrition, they can also be used to promote plant growth by stimulating plant hormone production. Although bacterial and fungal inoculants are common, inoculation with archaea to promote plant growth is being increasingly studied.

<i>Hydnellum caeruleum</i> Species of fungus

Hydnellum caeruleum, commonly known as the blue-gray hydnellum, blue-green hydnellum, blue spine, blue tooth, or bluish tooth, is an inedible fungus found in North America, Europe, and temperate areas of Asia.

<i>Suillus brevipes</i> Species of edible fungus in the family Suillaceae found throughout North America

Suillus brevipes is a species of fungus in the family Suillaceae. First described by American mycologists in the late 19th century, it is commonly known as the stubby-stalk or the short-stemmed slippery Jack. The fruit bodies (mushrooms) produced by the fungus are characterized by a chocolate to reddish-brown cap covered with a sticky layer of slime, and a short whitish stipe that has neither a partial veil nor prominent, colored glandular dots. The cap can reach a diameter of about 10 cm, while the stipe is up to 6 cm long and 2 cm thick. Like other bolete mushrooms, S. brevipes produces spores in a vertically arranged layer of spongy tubes with openings that form a layer of small yellowish pores on the underside of the cap.

<span class="mw-page-title-main">Hartig net</span> Network of inward-growing hyphae

The Hartig net is the network of inward-growing hyphae, that extends into the plant host root, penetrating between plant cells in the root epidermis and cortex in ectomycorrhizal symbiosis. This network is the internal component of fungal morphology in ectomycorrhizal symbiotic structures formed with host plant roots, in addition to a hyphal mantle or sheath on the root surface, and extramatrical mycelium extending from the mantle into the surrounding soil. The Hartig net is the site of mutualistic resource exchange between the fungus and the host plant. Essential nutrients for plant growth are acquired from the soil by exploration and foraging of the extramatrical mycelium, then transported through the hyphal network across the mantle and into the Hartig net, where they are released by the fungi into the root apoplastic space for uptake by the plant. The hyphae in the Hartig net acquire sugars from the plant root, which are transported to the external mycelium to provide a carbon source to sustain fungal growth.

<i>Lactarius alnicola</i> Species of fungus

Lactarius alnicola, commonly known as the golden milkcap, is a species of fungus in the family Russulaceae. The fruit bodies produced by the fungus are characterized by a sticky, vanilla-colored cap up to 20 cm (7.9 in) wide with a mixture of yellow tones arranged in faint concentric bands. The stem is up to 5 cm (2.0 in) long and has yellow-brown spots. When it is cut or injured, the mushroom oozes a white latex, which has an intensely peppery taste. The acrid taste of the fruit bodies renders them unpalatable. The fungus is found in the western United States and Mexico, where it grows in mycorrhizal associations with various coniferous trees species, such as spruce, pine and fir, and deciduous species such as oak and alder. It has also been collected in India. Two varieties have been named: var. pitkinensis, known from Colorado, and var. pungens, from Michigan.

<i>Suillus collinitus</i> Species of fungus

Suillus collinitus is a pored mushroom of the genus Suillus in the family Suillaceae. It is an edible mushroom found in European pine forests. The mushroom has a reddish to chestnut-brown cap that reaches up to 11 cm (4.3 in) in diameter, and a yellow stem measuring up to 7 cm (2.8 in) tall by 1 to 2 cm thick. On the underside of the cap are small angular pores, initially bright yellow before turning greenish-brown with age. A characteristic feature that helps to distinguish it from similar Suillus species, such as S. granulatus, is the pinkish mycelia at the base of the stem.

<i>Tricholoma vaccinum</i> Fungus of the agaric genus Tricholoma

Tricholoma vaccinum, commonly known as the russet scaly tricholoma, the scaly knight, or the fuzztop, is a fungus of the agaric genus Tricholoma. It produces medium-sized fruit bodies (mushrooms) that have a distinctive hairy reddish-brown cap with a shaggy margin when young. The cap, which can reach a diameter of up to 6.5 cm (2.6 in) wide, breaks up into flattened scales in maturity. It has cream-buff to pinkish gills with brown spots. Its fibrous, hollow stipe is white above and reddish brown below, and measures 4 to 7.5 cm long. Although young fruit bodies have a partial veil, it does not leave a ring on the stipe.

<span class="mw-page-title-main">Mycorrhizal network</span> Underground fungal networks that connect individual plants together

Mycorrhizal associations have profoundly impacted the evolution of plant life on Earth ever since the initial adaptation of plant life to land. In evolutionary biology, mycorrhizal symbiosis has prompted inquiries into the possibility that symbiosis, not competition, is the main driver of evolution.

<span class="mw-page-title-main">Mycorrhizal fungi and soil carbon storage</span> Terrestrial ecosystem

Soil carbon storage is an important function of terrestrial ecosystems. Soil contains more carbon than plants and the atmosphere combined. Understanding what maintains the soil carbon pool is important to understand the current distribution of carbon on Earth, and how it will respond to environmental change. While much research has been done on how plants, free-living microbial decomposers, and soil minerals affect this pool of carbon, it is recently coming to light that mycorrhizal fungi—symbiotic fungi that associate with roots of almost all living plants—may play an important role in maintaining this pool as well. Measurements of plant carbon allocation to mycorrhizal fungi have been estimated to be 5 to 20% of total plant carbon uptake, and in some ecosystems the biomass of mycorrhizal fungi can be comparable to the biomass of fine roots. Recent research has shown that mycorrhizal fungi hold 50 to 70 percent of the total carbon stored in leaf litter and soil on forested islands in Sweden. Turnover of mycorrhizal biomass into the soil carbon pool is thought to be rapid and has been shown in some ecosystems to be the dominant pathway by which living carbon enters the soil carbon pool.

<span class="mw-page-title-main">Ectomycorrhiza</span> Non-penetrative symbiotic association between a fungus and the roots of a vascular plant

An ectomycorrhiza is a form of symbiotic relationship that occurs between a fungal symbiont, or mycobiont, and the roots of various plant species. The mycobiont is often from the phyla Basidiomycota and Ascomycota, and more rarely from the Zygomycota. Ectomycorrhizas form on the roots of around 2% of plant species, usually woody plants, including species from the birch, dipterocarp, myrtle, beech, willow, pine and rose families. Research on ectomycorrhizas is increasingly important in areas such as ecosystem management and restoration, forestry and agriculture.

<span class="mw-page-title-main">Ectomycorrhizal extramatrical mycelium</span>

Ectomycorrhizal extramatrical mycelium is the collection of filamentous fungal hyphae emanating from ectomycorrhizas. It may be composed of fine, hydrophilic hypha which branches frequently to explore and exploit the soil matrix or may aggregate to form rhizomorphs; highly differentiated, hydrophobic, enduring, transport structures.

Dark septate endophytes (DSE) are a group of endophytic fungi characterized by their morphology of melanized, septate, hyphae. This group is likely paraphyletic, and contain conidial as well as sterile fungi that colonize roots intracellularly or intercellularly. Very little is known about the number of fungal taxa within this group, but all are in the Ascomycota. They are found in over 600 plant species and across 114 families of angiosperms and gymnosperms and co-occur with other types of mycorrhizal fungi. They have a wide global distribution and can be more abundant in stressed environments. Much of their taxonomy, physiology, and ecology are unknown.

<i>Rhizopogon occidentalis</i> Species of fungus

Rhizopogon occidentalis is an ectomycorrhizal fungus in the family Rhizopogonaceae of the Basidiomycota. It occurs most commonly in western North America in association with two-needle and three-needle pine hosts. They are false truffles with fruiting bodies that are yellow on the surface and pale yellow inside. Their edibility is disputed.

Orchid mycorrhizae are endomycorrhizal fungi which develop symbiotic relationships with the roots and seeds of plants of the family Orchidaceae. Nearly all orchids are myco-heterotrophic at some point in their life cycle. Orchid mycorrhizae are critically important during orchid germination, as an orchid seed has virtually no energy reserve and obtains its carbon from the fungal symbiont.

References

  1. 1 2 3 4 5 6 7 National Audubon Society field guide to North American mushrooms. Knopf. 1981. p. 413. ISBN   0-394-51992-2.
  2. 1 2 3 4 Petrzik, Karel; Sarkisova, Tatiana; Starý, Josef; Koloniuk, Igor; Hrabáková, Lenka; Kubešová, Olga (February 2016). "Molecular characterization of a new monopartite dsRNA mycovirus from mycorrhizal Thelephora terrestris (Ehrh.) and its detection in soil oribatid mites (Acari: Oribatida)". Virology. 489: 12–19. doi: 10.1016/j.virol.2015.11.009 . PMID   26700067.
  3. Radulović, Niko; Quang, Dang Ngoc; Hashimoto, Toshihiro; Nukada, Makiko; Tanaka, Masami; Asakawa, Yoshinori (2005). "Pregnane-Type Steroids from the Inedible Mushroom Thelephora terrestris". Chemical & Pharmaceutical Bulletin. 53 (3): 309–312. doi: 10.1248/cpb.53.309 . PMID   15744104.
  4. "Mycobank: Thelephora terrestris". Mycobank. Retrieved 2021-02-19.
  5. 1 2 Burt, Edward Angus (May 1914). "The Thelephoraceae of North America. I". Annals of the Missouri Botanical Garden. 1 (2): 185–227. doi:10.2307/2989992. JSTOR   2989992.
  6. 1 2 3 4 Ellis, Martin B.; Ellis, J. Pamela (1990). Fungi without gills (hymenomycetes and gasteromycetes) : an identification handbook (1st ed.). Britain: Chapman and Hall. ISBN   0-412-36970-2.
  7. 1 2 3 López-Gutiérrez, Araceli; Perez-Moreno, Jesus; Hernández-Santiago, Faustino; Uscanga-Mortera, Ebandro; García-Esteva, Antonio; Cetina-Alcalá, Victor Manuel; Cardoso-Villanueva, María del Rosario; Xoconostle-Cázares, Beatriz (19 June 2018). "Nutrient mobilization, growth and field survival of Pinus pringlei inoculated with three ectomycorrhizal mushrooms". Botanical Sciences. 96 (2): 286. doi: 10.17129/botsci.1239 .
  8. Moeller, Holly V.; Peay, Kabir G. (27 July 2016). "Competition-function tradeoffs in ectomycorrhizal fungi". PeerJ. 4: e2270. doi: 10.7717/peerj.2270 . PMC   4974999 . PMID   27547573.
  9. 1 2 3 Smith, Sally E; Read, David J (2002). Mycorrhizal Symbiosis. Academic Press. pp. 470–489. doi:10.1016/B978-012652840-4/50018-8.
  10. Hilszczańska, Dorota; Małecka, Monika; Sierota, Zbigniew (January 2008). "Changes in nitrogen level and mycorrhizal structure of Scots pine seedlings inoculated with Thelephora terrestris" (PDF). Annals of Forest Science. 65 (4): 409. doi:10.1051/forest:2008020. S2CID   21922463.
  11. Veselá, Petra; Vašutová, Martina; Edwards-Jonášová, Magda; Cudlín, Pavel (29 January 2019). "Soil Fungal Community in Norway Spruce Forests under Bark Beetle Attack". Forests. 10 (2): 109. doi: 10.3390/f10020109 .
  12. Agerer, R.; Weiss, M. (29 August 2018). "Studies on Ectomycorrhizae. XX. Mycorrhizae Formed by on Norway Spruce". Mycologia. 81 (3): 444–453. doi:10.1080/00275514.1989.12025766.
  13. 1 2 Davis, R. Michael; Sommer, Robert; Menge, John A. (2012). Field Guide to Mushrooms of Western North America. Berkeley: University of California Press. pp. 310–311. ISBN   978-0-520-95360-4. OCLC   797915861.
  14. Trudell, Steve; Ammirati, Joe (2009). Mushrooms of the Pacific Northwest. Timber Press Field Guides. Portland, OR: Timber Press. p. 253. ISBN   978-0-88192-935-5.
  15. Birraux, D.; Fries, N. (November 1981). "Germination of basidiospores". Canadian Journal of Botany. 59 (11): 2062–2064. doi:10.1139/b81-267.