Bothia | |
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Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Fungi |
Division: | Basidiomycota |
Class: | Agaricomycetes |
Order: | Boletales |
Family: | Boletaceae |
Genus: | Bothia Halling, T.J.Baroni & Manfr.Binder (2007) |
Species: | B. castanella |
Binomial name | |
Bothia castanella (Peck) Halling, T.J.Baroni & Manfr.Binder (2007) | |
Synonyms [1] [2] [3] | |
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Bothia castanella | |
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Pores on hymenium | |
Cap is convex or flat | |
Hymenium is decurrent | |
Stipe is bare | |
Spore print is yellow-brown | |
Ecology is mycorrhizal | |
Edibility is unknown |
Bothia is a fungal genus in the family Boletaceae. A monotypic genus, it contains the single species Bothia castanella, a bolete mushroom first described scientifically in 1900 from collections made in New Jersey. Found in the eastern United States, Costa Rica, China, and Taiwan, it grows in a mycorrhizal association with oak trees. Its fruit body is chestnut brown, the cap is smooth and dry, and the underside of the cap has radially elongated tubes. The spore deposit is yellow-brown. The edibility of the mushroom is unknown. Historically, its unique combination of morphological features resulted in the transfer of B. castanella to six different Boletaceae genera. Molecular phylogenetic analysis, published in 2007, demonstrated that the species was genetically unique enough to warrant placement in its own genus.
Phylogeny of B. castanella and related boletus based on nuclear large subunit (LSU) ribosomal DNA sequences. [3] |
The bolete was first named Boletinus castanellus by American mycologist Charles Horton Peck in 1900. The type was collected in New Jersey by botanist Edward Sterling. [4] William Alphonso Murrill transferred it to Boletinellus in 1909; his generic concept of Boletinus included a ring on the stipe. [5] Rolf Singer placed it in Gyrodon in 1938, [6] while Wally Snell and Esther Dick thought the species to be more appropriately placed in Xerocomus , and transferred it to that genus in 1958. [7] Alexander H. Smith and Harry D. Thiers moved it to Suillus in their 1964 treatment of North American species. [8] In more recent history (1996), it has been moved to Chalciporus . [9] Snell and Dick's Boletinus squarrosoides (later moved by different authors to Phylloporus , Xerocomus, and Chalciporus) [10] is a facultative synonym (based on a different type) of B. castanella. [1] In their original 1936 publication, they compared the two species, and noted that Boletinus squarrosoides differed from B. castanellus by "reddish brown color, terete scaliness, and yellow colors of the flesh, tubes and stipe". [11] By 1958, after having examined additional collections, they realized that the two species were conspecific and represented morphological variations of each other. [7]
In 2007, Roy Halling and colleagues published molecular analysis showing that the species was genetically and morphologically distinct enough to deserve placement in a new Boletaceae genus, which they named Bothia. Since the original type has been lost, they designated a neotype from a collection made in Reading, Pennsylvania. Bothia is named in honor of mycologist Ernst E. Both, formerly curator emeritus of the Buffalo Museum of Science, and "promoter, facilitator and consummate student of boletology". [3] The specific epithet castanella, which means "small chestnut", refers to the color of the cap. [12]
The cap of Bothia castanella is convex at first before flattening out in age, reaching a diameter of 3–8 cm (1.2–3.1 in). The center of the cap sometimes acquires a shallow depression, while the margin ranges from even to wavy and irregular. The cap surface is dry and initially hairy, but becomes smooth in maturity. Its color ranges from reddish brown to burgundy-brown to dark yellowish brown. [13] The flesh is white, and, unlike several other bolete species, does not change color when bruised or injured. It is about 8 mm (0.3 in) thick. [8]
On the cap undersurface are the pores, which are angular to elongated and measure about 2 mm wide. The color of the pore surface is pinkish brown to tan or buff, but it becomes yellowish brown in maturity; bruised areas turn ochre-tawny. The tubes are somewhat decurrent attached to the stipe (i.e., running slightly down its length), and extend about 6 mm (0.24 in) deep. The mushroom lacks any appreciable odor or taste. The dry, solid stipe measures 2–7 cm (0.8–2.8 in) long by 0.6–2 cm (0.2–0.8 in) thick, and is nearly equal in thickness throughout, or slightly tapered on either end. Its surface is more or less smooth except for a reticulate (meshed) area at the apex. The edibility of the mushroom is unknown. [13]
Fruit bodies produce a yellow-brown spore print. Spores are egg-shaped to ellipsoid, smooth, thin-walled, and measure 8.4–10.5 by 4.2–4.9 μm. The basidia (spore-bearing cells) are club-shaped, four-spored, and measure 25–35 by 7–9 μm. Cystidia are present on both the tube walls (as pleurocystidia) and abundantly on the edges (as cheilocystidia). They are somewhat spindle-shaped, sometimes with a central swelling, and measure 45–70 by 7–12 μm. Clamp connections are absent from the hyphae, [3] and all of the hyphae are inamyloid. [8]
Several chemical tests can used to help confirm identification of the mushroom. The cap cuticle turns grayish with the application of a drop of ferrous sulfate (FeSO4), and dark brown to amber with a dilute solution of potassium hydroxide (KOH). The flesh turns pale brown with KOH, and pale yellow with ammonia (NH4OH). [13]
The fruit bodies of Bothia castanella grow singly, scattered, or in groups under oak, although other trees such as birch, beech, hickory, eastern white pine, and hemlock are sometimes present in the area. [3] Typical habitats include woods and parklands. [12] In Asia it has been recorded growing in bamboo forests. [14]
In the United States, where the fruiting season occurs from July to October, [13] its range extends from the Carolinas north to New York and New England, and west to Minnesota. [3] It has also been collected from Costa Rica, [9] China, [15] and Taiwan. [14]
Chalciporus piperatus, commonly known as the peppery bolete, is a small pored mushroom of the family Boletaceae found in mixed woodland in Europe and North America. It has been recorded under introduced trees in Brazil, and has become naturalised in Tasmania and spread under native Nothofagus cunninghamii trees. A small bolete, the fruit body has a 1.6–9 cm orange-fawn cap with cinnamon to brown pores underneath, and a 4–9.5 cm high by 0.6–1.2 cm thick stipe. The flesh has a very peppery taste. The rare variety hypochryseus, found only in Europe, has yellow pores and tubes.
Boletellus is a genus of fungi in the family Boletaceae. The genus has a widespread distribution, especially in subtropical regions, and contains about 50 species. The genus was first described by American mycologist William Alphonso Murrill in 1909. The genus name means "small Boletus".
Chalciporus is a genus of fungi in the family Boletaceae. There are approximately 25 species in the genus.
Aureoboletus mirabilis, commonly known as the admirable bolete, the bragger's bolete, and the velvet top, is an edible species of fungus in the Boletaceae mushroom family. The fruit body has several characteristics with which it may be identified: a dark reddish-brown cap; yellow to greenish-yellow pores on the undersurface of the cap; and a reddish-brown stem with long narrow reticulations. Aureoboletus mirabilis is found in coniferous forests along the Pacific Coast of North America, and in Asia. Unusual for boletes, A. mirabilis sometimes appears to fruit on the wood or woody debris of Hemlock trees, suggesting a saprobic lifestyle. Despite the occasional appearances to the contrary, Aureoboletus mirabilis is mycorrhizal, and forms a close association with the tree's roots.
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.
Suillus sibiricus is a mushroom-forming fungus in the family Suillaceae. It is found in mountains of Europe, North America, and Siberia, strictly associated with several species of pine tree. Due to its specific habitat and rarity in Europe, it has been selected for inclusion in several regional Red Lists. Its fruit bodies are characterised by having slimy caps in wet weather, which can reach diameters of up to 10 cm (3.9 in). On the underside of the cap are yellow angular pores that bruise a pinkish to cinnamon colour. The stem is up to 8 cm (3.1 in) tall and 2.5 cm (1.0 in) wide and typically has a ring, a remnant of the partial veil that covers the fruit body in its early development. In North America, it is commonly called the Siberian slippery jack. Phylogenetic analysis has shown that S. sibiricus is closely related to S. umbonatus and S. americanus, and may in fact be conspecific with the latter species.
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.
Suillus salmonicolor, commonly known as the Slippery Jill, is a fungus in the family Suillaceae of the order Boletales. First described as a member of the genus Boletus in 1874, the species acquired several synonyms, including Suillus pinorigidus and Suillus subluteus, before it was assigned its current binomial name in 1983. It has not been determined with certainty whether S. salmonicolor is distinct from the species S. cothurnatus, described by Rolf Singer in 1945. S. salmonicolor is a mycorrhizal fungus—meaning it forms a symbiotic association with the roots of plants such that both organisms benefit from the exchange of nutrients. This symbiosis occurs with various species of pine, and the fruit bodies of the fungus appear scattered or in groups on the ground near the trees. The fungus is found in North America, Hawaii, Asia, the Caribbean, South Africa, Australia and Central America. It has been introduced to several of those locations via transplanted trees.
Tylopilus alboater, called the black velvet bolete, by some, is a bolete fungus in the family Boletaceae. The species is found in North America east of the Rocky Mountains, and in eastern Asia, including China, Japan, Taiwan, and Thailand. A mycorrhizal species, it grows solitarily, scattered, or in groups on the ground usually under deciduous trees, particularly oak, although it has been recorded from deciduous, coniferous, and mixed forests.
Boletus curtisii is a species of fungus in the family Boletaceae. It produces small- to medium-sized fruit bodies (mushrooms) with a convex cap up to 9.5 cm (3.7 in) wide atop a slender stem that can reach a length of 12 cm (4.7 in). In young specimens, the cap and stem are bright golden yellow, although the color dulls to brownish when old. Both the stem and cap are slimy or sticky when young. On the underside of the cap are small circular to angular pores. The mushroom is edible, but not appealing. It is found in eastern and southern North America, where it grows in a mycorrhizal association with hardwood and conifer trees. Once classified as a species of Pulveroboletus, the yellow color of B. curtisii is a result of pigments chemically distinct from those responsible for the yellow coloring of Pulveroboletus.
Xerocomus illudens is a species of bolete fungus in the family Boletaceae. Described as new to science in 1898, it is found in Asia and North America, where it grows in a mycorrhizal association with oak.
Aureoboletus projectellus is a species of bolete fungus in the family Boletaceae. Found in North America, and recently in Europe, it grows in a mycorrhizal association with pine trees.
Boletinellus merulioides, commonly known as the ash-tree bolete, is a species of bolete fungus in the family Boletinellaceae. Described as new to science in 1832, it is found in Asia and eastern North America, where it grows on the ground near ash trees.
Buchwaldoboletus lignicola is a species of bolete fungus in the family Boletaceae native to Europe and North America. Found on wood, it is actually parasitic on the fungus Phaeolus schweinitzii. It has a convex yellow- to rusty brown cap, yellow to yellow-brown pores and stipe, and a brown spore print. Its edibility is unknown.
Chalciporus pseudorubinellus is a bolete fungus of the family Boletaceae. It is found in North America and Central America.
Harrya chromapes, commonly known as the yellowfoot bolete or the chrome-footed bolete, is a species of bolete fungus in the family Boletaceae. The bolete is found in eastern North America, Costa Rica, and eastern Asia, where it grows on the ground, in a mycorrhizal association with deciduous and coniferous trees. Fruit bodies have smooth, rose-pink caps that are initially convex before flattening out. The pores on the cap undersurface are white, aging to a pale pink as the spores mature. The thick stipe has fine pink or reddish dots (scabers), and is white to pinkish but with a bright yellow base. The mushrooms are edible but are popular with insects, and so they are often infested with maggots.
Tylopilus peralbidus is a bolete fungus in the family Boletaceae native to the eastern United States.
Suillus subaureus is a rare species of bolete fungus in the family Suillaceae. It is found in North America, where it associates with deciduous trees. Originally described in 1887 by Charles Horton Peck, it was transferred to genus Suillus by Wally Snell in 1944. Fruitbodies are pale yellow—reflecting its specific epithet subaureus, which means "somewhat golden yellow". The spore print is olive brown. Spores are smooth and inamyloid, and measure 7–10 by 2.7–3.5 μm. It has also been recorded in Taiwan.
Imleria badia, commonly known as the bay bolete, is an edible, pored mushroom found in Eurasia and North America, where it grows in coniferous or mixed woods on the ground or on decaying tree stumps, sometimes in prolific numbers. Both the common and scientific names refer to the bay- or chestnut-coloured cap, which is almost spherical in young specimens before broadening and flattening out to a diameter up to 15 cm (6 in). On the cap underside are small yellowish pores that turn dull blue-grey when bruised. The smooth, cylindrical stipe, measuring 4–9 cm long by 1–2 cm thick, is coloured like the cap, but paler. Some varieties have been described from eastern North America, differing from the main type in both macroscopic and microscopic morphology.
Chalciporus rubinellus, commonly known as the purple-red bolete, is a bolete fungus of the family Boletaceae. It was first described in 1879 as Boletus rubinellus, and later transferred to the genus Chalciporus in 1973.