Suillus pungens

The fungus was first described scientifically by American mycologists Harry D. Thiers and Alexander H. Smith in their 1964 monograph on North American Suillus species. The type collection was made on the campus of San Francisco State University in San Francisco.[1] Smith and Thiers classified S. pungens in section Suilli—a grouping of related species characterized by the presence of either a ring on the stipe, a partial veil adhering to the cap margin, or a "false veil" not attached to the stipe but initially covering the tube cavity.[2]

A 1996 molecular analysis of 38 different Suillus species used the sequences of their internal transcribed spacers to infer phylogenetic relationships and clarify the taxonomy of the genus. The results suggest that S. pungens was genetically similar to S. collinitus, S. neoalbidipes, S. pseudobrevipes, S. luteus, S. brevipes, S. weaverae, and certain isolates of S. granulatus.[3]

The specific epithet is derived from the Latin pungens,[4] and refers to the pungent aroma of the fruit bodies. The mushroom is commonly known as the "pungent slippy jack"[5] or the "pungent suillus".[6] It has also been referred to as the "slippery jack",[7] a common name applied to several Suillus species.

The stipe is covered with irregularly shaped glandular dots.

The cap of S. pungens is roughly convex when young, becoming plano-convex (flat on one side and rounded on the other) to somewhat flat with age, and reaches diameters of 4–14 cm (1.6–5.5 in). The cap surface is sticky to slimy when moist, becoming shiny when dried. The surface is smooth but is sometimes streaked with the sticky glue-like cap slime when older. The cap color is highly variable in this species, and the cap is often variegated with a mixture of light and dark colors. When young it is dirty-white to olive with pale olive splotches. Maturing caps can retain the color they had when young, or become tawny to orange-yellow to reddish-brown, or a combination of these colors.[6] The cap margin is initially rolled inward and has a cottony roll of white tissue, but becomes naked and curves downward with age. The flesh is 1–2 cm (0.4–0.8 in) thick, white and unchanging in young fruit bodies, frequently changing to yellow when older.[1]

Young fruit bodies are covered with milky droplets on their pore surfaces.

The tubes that comprise the hymenium (spore-bearing tissue) on the underside of the cap are up to 1 cm (0.4 in) long, adnate when young, becoming decurrent or nearly so with age. In young specimens, they are whitish to pale buff, and are covered with milky droplets that become brown to ochraceous when dried. As specimens mature the color of the pore surface changes to yellowish, and finally to dark yellow. The angular pores, which are 1–1.5 mm in diameter, are not radially arranged, and do not change color when bruised.[1] The stipe is solid (rather than hollow), 3–7 cm (1.2–2.8 in) long, and 1–2 cm (0.4–0.8 in) thick near the top. Its shape is variable: either roughly equal in width throughout, thicker at the base, or somewhat thicker in the middle. Its surface is dry and smooth, and covered with irregularly shaped glandular dots. The dots—minute clumps of pigmented cells—are initially reddish before becoming brownish. The background color of the stipe is initially whitish (roughly the same color as the tubes), but becomes more yellow with age. It does not change color when bruised, and does not have a ring. The flesh of the stipe is white, and does not change color when exposed to air.[1]

The spore print is olive-brown to pale cinnamon-brown.[5] Individual spores are thin-walled, hyaline (translucent), and smooth. Their shape is ellipsoid to roughly cylindrical in face view or inequilateral when viewed in profile, and they measure 9.5–10 by 2.8–3.5 μm. The basidia (spore-bearing cells of the hymenium) are hyaline, club-shaped and four-spored, with dimensions of 33–36 by 8–10 μm. The thin-walled cystidia are rare to scattered on the tube surface but abundant on the pores, where they usually occur in massive clusters. They appear dark brown when mounted in a dilute (3%) solution of potassium hydroxide (KOH), and are cylindric to roughly club-shaped, measuring 43–79 by 7–10 μm. They are usually encrusted with pigment, although some may be hyaline. The tissue comprising the tube is hyaline, and made of divergent to nearly parallel hyphae that are 3–5 μm wide. The pileipellis is a tissue type known as an ixotrichodermium (made of interwoven gelatinized hyphae); it stains brown in KOH, and is made of hyphae that are 4–5 μm wide. The stipe cuticle is made of clusters of cystidia similar to those found in the hymenium. Clamp connections are absent in the hyphae of S. pungens.[1]

Several chemical tests can be employed in the field to aid in the identification of S. pungens. With an application of a drop of KOH, the flesh will turn vinaceous (the color of red wine), the tubes red, the cap cuticle black, and the stipe cuticle pale vinaceous. With ammonium hydroxide (NH₄OH), the flesh becomes very pale vinaceous, and the tubes turn bright red. Iron(II) sulfate (FeSO₄) turns the flesh gray, the tubes dark gray to black, and the stipe cuticle light gray.[1]

Similar species

Suillus granulatus

Suillus placidus

Suillus pungens is characterized by the very distinct color changes that occur in the cap as it develops. The range of color variation makes it possible to misidentify the species with others whose color overlaps. Suillus pungens has been misidentified as S. placidus because of the white color of the young fruit bodies and the droplets of exudate. S. placidus has a wider distribution, is usually found in association with eastern white pine, is generally smaller, with a maximum cap diameter up to 9 cm (3.5 in), and has smaller spores, measuring 7–9 by 2.5–3.2 μm. It does not have any distinctive taste or odor.[9] North American S. granulatus is another potential lookalike species, and at maturity it is nearly identical to Suillus pungens. The cap of S. granulatus is variable in color, ranging from pale yellow to various shades of brown, while the pore surface is initially whitish, later becoming yellowish, and similar to S. placidus, its typical host is eastern white pine. Unlike S. pungens, it lacks a characteristic odor and taste.[6] The Californian species Suillus glandulosipes has veil material attached to the edge of the cap when young. It also lacks the distinctive changes in cap color during development, is associated with lodgepole pine, has smaller spores (6.6–8.8 by 2.5–3 μm), and lacks any obvious taste and odor. Another Californian species, Suillus quiescens, newly described in 2010, may resemble S. pungens, especially at maturity. S. quiescens can be distinguished by its lack of white or olive colors when young and by a less glandular stipe when mature.[10]

S. pungens is often found growing near Chroogomphus vinicolor (pictured).

Suillus pungens is an ectomycorrhizal (EM) basidiomycete that forms symbiotic relationships almost exclusively with Monterey pine (Pinus radiata) and bishop pine (Pinus muricata); some collections have been made under knobcone pine (Pinus attenuata)[1] and ponderosa pine (Pinus ponderosa), but only within the range of Monterey pine.[5] All these trees have small scattered natural ranges largely restricted to California.[11] An EM symbiosis is a mutualistic relationship between an EM fungus and the root tip of a compatible EM plant. The fruit bodies of Suillus pungens grow solitarily, scattered or in groups in humus. They are often found growing near fruit bodies of Chroogomphus vinicolor[7] and Helvella lacunosa.[5] Suillus pungens is often the most abundant Suillus in the San Francisco Bay Area. The type collection was made on the campus of San Francisco State University in San Francisco, where it occurs in abundance during the fall and winter seasons. Although it occurs most frequently in the autumn and winter,[5] it is one of the few species of Suillus that continue to fruit sporadically throughout the year,[1] especially in wet weather.[5] It has also been identified in the southeastern Sierra Nevada[12] and on Santa Cruz Island.[13]

Ectomycorrhizal associates of S. pungens include Monterey pine (above) and bishop pine (below).

A genet is a group of genetically identical individuals that have grown in a given location, all originating vegetatively from a single ancestor. Once established, genets vegetatively spread hyphae out from the root tip into the soil and may connect two or more trees to form a network of mycorrhizae. In field studies, the approximate size of fungal genets is typically estimated by collecting and mapping fruit bodies on a site, determining which fruit bodies are genetically identical by either somatic incompatibility (a method fungi use to distinguish self from non-self by delimiting their own mycelia from that of other individuals of the same species) or various molecular techniques, and then determining the distance between identical fruit bodies.[14] In a 1996 study, mycologists Monique Gardes and Thomas Bruns hypothesized that S. pungens, an abundant fruiter in pine forests, would be dominant on the roots of the pine trees. However, by sampling underground ectomycorrhizae in addition to above-ground fruit bodies, they found that the fungus can fruit prolifically while occupying only a small fraction of the ectomycorrhizal root assemblage, which was otherwise dominated by Russula species and Tomentella sublilacina.[15][16] Gardes and Bruns hypothesized that the disparity between above- and below-ground representation may be because the fungus invests less energy in vegetative growth and persistence and more in fruiting, or alternatively, because the species is particularly efficient at acquiring carbon from its hosts and so needs to colonize only a few rootlets to obtain enough to allow abundant fruiting.[15] A 1998 study by Pierluigi Bonello and colleagues used single-strand conformation polymorphism analysis to detect minute genetic differences among S. pungens genets, and showed that most of the fruiting occurred from a single large genet. This result indicates that the fungus persists because of extensive vegetative growth, rather than frequent establishment of new genets from spores, and that it uses carbon resources efficiently.[17] The study also described an S. pungens genet with an area of approximately 300 m² (3,200 sq ft) and a span greater than 40 m (130 ft) across, which was at the time the largest EM fungal genet reported.[17] The large S. pungens genet was not detected after wildfire, demonstrating that it did not survive in the absence of a host, and suggesting that spores are the primary means by which the fungus recolonizes after a fire.[16]

• List of North American boletes

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• Suillus pungens in Index Fungorum