Rhizopogon salebrosus

Last updated

Rhizopogon salebrosus
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Fungi
Division: Basidiomycota
Class: Agaricomycetes
Order: Boletales
Family: Rhizopogonaceae
Genus: Rhizopogon
Species:
R. salebrosus
Binomial name
Rhizopogon salebrosus

Rhizopogon salebrosus is a mushroom species within the Rhizopogon subgenus Amylopogon . R.salebrosus is a monotropoid mycorrhiza that is of vital importance to the ecology of conifer forests, especially in the Pacific Northwest region of North America. [1] Although it is native to North America, R. salebrosus has been found in Europe and its range is generally limited to mountainous regions with sufficient precipitation. [2] The mycoheterotrophic plant, Pterospora andromedea is often found in an obligate association with R. salebrosus in western parts of the U.S. Eastern populations of P. andromedea are typically symbiotic with another Rhizopogon sub species, R. kretzerae. [3]

Rhizopogon sp. from Sierra de Valdemeca, Cuenca, Spain Rhizopogon re soil.jpg
Rhizopogon sp. from Sierra de Valdemeca, Cuenca, Spain

Species that form these mycoheterotrophic relationships like P. andromedea and R. salebrosus benefit one other by sharing essential nutrients. For example, ectomychorrizal plants contribute up to 30% of their fixed carbon in exchange for nitrogen that their host fungi absorb from the soil. These unique mycoheterotrophic associations are thought to have evolved due to low light availability on the forest floor. [4]

Competition among ectomycorrhizal species plays an influential role in the composition and distribution of Rhizopogon species and the plants they associate with. Abiotic factors such as soil chemistry and soil moisture affect ectomychorrizal assemblages, however much less is known about the biotic factors that determine their composition other than host specificity. One study compared the competitive advantage between Rhizopogon salebrosus and Rhizopogon occidentalis. Each Rhizopogon species was introduced to Pinus muricata seedlings and the root tip biomass of each species was determined every few months. This was possible because a number of seedlings were planted in microcosms with only R. salebrosus, only R. occidentalis, or both R. salebrosus and R. occidentalis and grown under the same conditions. Some seedlings were then harvested every 2 months, the soil was rinsed from the root mass, and then the percentage of fungal occupation of their roots was determined using molecular sequencing. They found that R. occidentalis had similar root tip biomass when grown alone or in the presence of R. salebrosus. However, R. salebrosus had significantly less root tip biomass when grown in the presence of R. occidentalis than when grown alone, indicating it as a competitive inferior. [5] Another study involving the same two Rhizopogon species examined the beneficial effects they imparted to their host plant. They found no significant difference in growth, survival, or percentage leaf nitrogen of seedlings colonized with either R. salebrosus or R. occidentalis. However, plants inoculated with both ectomychorrizal species showed significantly higher growth and percent leaf nitrogen compared to seedlings without ectomychorrizal fungus. [6] Another interesting aspect of ectomycorrhizal competition are the strategies used to persist over long periods and colonize during unfavorable conditions such as drought or wildfire. Fungi are able to disperse and propagate with the help of spores and sclerotia which are able to remain dormant in the soil for some time, although their longevity is not well understood. In one a study the viability of fungal propagules was tested by collecting soil samples from the forest and aging them for six years. While the colonization rate was low, R. salebrosus was identified as a species able to survive in the soil for at least six years. [7]

Distribution of species is a prevalent topic, especially as climate change continues to alter forest ecosystems. Within the Deschutes National Forest, Oregon, USA, the historic range of Pinus contorta is steadily changing due to increasing temperatures and drought, declines in winter precipitation and snowpack. These environmental changes may have facilitated the migration of Pinus ponderosa into P. contorta territory. Observations such as these have led to studies examining the relationship between pine species distribution and how they are aided through the fungal composition of the soil. It has been confirmed that R. salebrosus is one of the dominant fungal symbionts in both P. contorta and P. ponderosa. [8] These findings indicate that the successful migration of pine species may be influenced by the previous distribution or co-migration of ectomycorrhizal fungi.

Fire is known to significantly reduce biomass and diversity of ectomychorrizal fungi. Though some species are more persistent than others. One study found that R. salebrosus was present in the soil before and after prescribed burning, suggesting that it is able to survive or re-establish quickly after a disturbance such as fire. [9]

Rhizopogon kretzerae is another ectomycorrhizal fungus under the Rhizopogon subgenus Amylopogon. R. kretzerae are similar to R. salebrosus in that they form obligate symbiotic relationships with Pterospora andromedea, however these associations are usually only observed in eastern populations. [10] Like other members of the subgenus Amylopogon, R. kretzerae is known to act as a mycobiont host to the parasitic plant P. andromedea and grow under members of Pinaceae , however it has only ever been found associated with Pinus strobus or the eastern white pine. In recent years there has been a noticeable decline in eastern populations of P. andromedea likely due to human impact. Conservation management efforts are being made by examining the genetics of P. andromedea's preferred eastern fungal symbiont, R. kretzerae. [3] In many cases, mycoheterotrophic plants and mycorrhizal fungal relationships are so specific that seedling recruitment is not possible in the absence of their key fungal symbiont. Close relatives of the host fungi are sometimes able to trigger germination, though survivorship is low. [4]

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>Pinus cembra</i> Species of plant

Pinus cembra, also known as Swiss pine, Swiss stone pine, Arolla pine, Austrian stone pine, or just stone pine, is a species of pine tree in the subgenus Strobus.

<i>Pterospora</i> Genus of plants

Pterospora, commonly known as pinedrops, woodland pinedrops, Albany beechdrops, or giant bird's nest, is a North American genus in the subfamily Monotropoideae of the heath family, and includes only the species Pterospora andromedea. It grows as a mycoheterotroph in coniferous or mixed forests. It is widespread across much of Canada as well as the western and northeastern United States to Mexico. Along with Monotropa it is one of the more frequently encountered genera of the Monotropoideae.

<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.

<i>Suillus bovinus</i> Species of edible fungus in the family Suillaceae native to Europe and Asia

Suillus bovinus, also known as the Jersey cow mushroom or bovine bolete, is a pored mushroom of the genus Suillus in the family Suillaceae. A common fungus native to Europe and Asia, it has been introduced to North America and Australia. It was initially described as Boletus bovinus by Carl Linnaeus in 1753, and given its current binomial name by Henri François Anne de Roussel in 1806. It is an edible mushroom, though not highly regarded.

<i>Epipogium aphyllum</i> Species of hardy myco-heterotrophic orchid lacking chlorophyll

Epipogium aphyllum, the ghost orchid, is a hardy mycoheterotrophic orchid lacking chlorophyll. It is one of the rarest representatives of Orchidae family.

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

Suillus quiescens is a pored mushroom of the genus Suillus in the family Suillaceae. First collected in 2002 on Santa Cruz Island off the coast of California, in association with Bishop Pine, the species was scientifically described and named in 2010. In addition to its distribution in coastal California, it was also found forming ectomycorrhizae with the roots of pine seedlings in the eastern Sierra Nevada, coastal Oregon, and the southern Cascade Mountains. It resembles Suillus brevipes, but can be distinguished from that species by its paler-colored immature cap and by the tiny colored glands on the stipe that darken with age.

<i>Suillus pungens</i> Species of fungus in the family Suillaceae found in California

Suillus pungens, commonly known as the pungent slippery jack or the pungent suillus, is a species of fungus in the genus Suillus. The fruit bodies of the fungus have slimy convex caps up to 14 cm (5.5 in) wide. The mushroom is characterized by the very distinct color changes that occur in the cap throughout development. Typically, the young cap is whitish, later becoming grayish-olive to reddish-brown or a mottled combination of these colors. The mushroom has a dotted stem (stipe) up to 7 cm (2.8 in) long, and 2 cm (0.8 in) thick. On the underside on the cap is the spore-bearing tissue consisting of minute vertically arranged tubes that appear as a surface of angular, yellowish pores. The presence of milky droplets on the pore surface of young individuals, especially in humid environments, is a characteristic feature of this species. S. pungens can usually be distinguished from other similar Suillus species by differences in distribution, odor and taste. The mushroom is considered edible, but not highly regarded.

<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.

<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.

<span class="mw-page-title-main">Monotropoideae</span> Subfamily of flowering plants in the heather family Ericaceae

Monotropoideae, sometimes referred to as monotropes, are a flowering plant subfamily in the family Ericaceae. Members of this subfamily are notable for their mycoheterotrophic and non-photosynthesizing or achlorophyllous characteristics.

<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.

<i>Thelephora terrestris</i> Species of fungus

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

Rhizopogon amylopogon is a sub-genus of Rhizopogon containing seven species.

References

  1. Dowie, Nicholas J.; Grubisha, Lisa C.; Burton, Brent A.; Klooster, Matthew R.; Miller, Steven L. (2017-01-02). "Increased phylogenetic resolution within the ecologically important Rhizopogon subgenus Amylopogon using 10 anonymous nuclear loci". Mycologia. 109 (1): 35–45. doi:10.1080/00275514.2017.1285165. ISSN   0027-5514. PMID   28402794. S2CID   12476105.
  2. Pietras, Marcin; Kolanowska, Marta (2019-06-01). "Predicted potential occurrence of the North American false truffle Rhizopogon salebrosus in Europe". Fungal Ecology. 39: 225–230. doi:10.1016/j.funeco.2018.12.002. ISSN   1754-5048. S2CID   109548347.
  3. 1 2 Grubisha, Lisa C.; Brewer, Jessica D.; Dowie, Nicholas J.; Miller, Steven L.; Trowbridge, Steven M.; Klooster, Matthew R. (2014). "Microsatellite primers for the fungi Rhizopogon kretzerae and R. salebrosus (Rhizopogonaceae) from 454 shotgun pyrosequencing". Applications in Plant Sciences. 2 (7): 1400029. doi:10.3732/apps.1400029. ISSN   2168-0450. PMC   4103475 . PMID   25202638.
  4. 1 2 Merckx, Vincent; Bidartondo, Martin I.; Hynson, Nicole A. (2009). "Myco-heterotrophy: when fungi host plants". Annals of Botany. 104 (7): 1255–1261. doi:10.1093/aob/mcp235. ISSN   1095-8290. PMC   2778383 . PMID   19767309.
  5. Kennedy, Peter G.; Bruns, Thomas D. (2005-02-08). "Priority effects determine the outcome of ectomycorrhizal competition between two Rhizopogon species colonizing Pinus muricata seedlings". New Phytologist. 166 (2): 631–638. doi: 10.1111/j.1469-8137.2005.01355.x . PMID   15819925.
  6. Kennedy, Peter G.; Bergemann, Sarah E.; Hortal, Sara; Bruns, Thomas D. (2006-11-29). "Determining the outcome of field-based competition between two Rhizopogon species using real-time PCR: FIELD COMPETITION BETWEEN ECTOMYCORRHIZAL FUNGI". Molecular Ecology. 16 (4): 881–890. doi:10.1111/j.1365-294X.2006.03191.x. PMID   17284218. S2CID   8276241.
  7. Nguyen, Nhu H.; Hynson, Nicole A.; Bruns, Thomas D. (2012). "Stayin' alive: survival of mycorrhizal fungal propagules from 6-yr-old forest soil". Fungal Ecology. 5 (6): 741–746. doi:10.1016/j.funeco.2012.05.006.
  8. Garcia, Maria O.; Smith, Jane E.; Luoma, Daniel L.; Jones, Melanie D. (2016). "Ectomycorrhizal communities of ponderosa pine and lodgepole pine in the south-central Oregon pumice zone". Mycorrhiza. 26 (4): 275–286. doi:10.1007/s00572-015-0668-x. ISSN   0940-6360. PMID   26547440. S2CID   14723930.
  9. Smith, Jane E.; McKAY, Donaraye; Brenner, Greg; McIVER, Jim; Spatafora, Joseph W. (2005-06-09). "Early impacts of forest restoration treatments on the ectomycorrhizal fungal community and fine root biomass in a mixed conifer forest: Prescribed fire and EMF species richness". Journal of Applied Ecology. 42 (3): 526–535. doi: 10.1111/j.1365-2664.2005.01047.x .
  10. Grubisha, Lisa C.; Dowie, Nicholas J.; Miller, Steven L.; Hazard, Christina; Trowbridge, Steven M.; Horton, Thomas R.; Klooster, Matthew R. (2014). "Rhizopogon kretzerae sp. nov.: the rare fungal symbiont in the tripartite system with Pterospora andromedea and Pinus strobus". Botany. 92 (7): 527–534. doi:10.1139/cjb-2013-0309. ISSN   1916-2790.