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Blue Chanterelle (Polyozellus multiplex)

Blue Chanterelle Mushroom Species Guide

Blue Chanterelle (Polyozellus multiplex)

Blue Chanterelle (Polyozellus multiplex) is an edible wild mushroom native to old-growth spruce-fir forests across northern North America and East Asia, producing stunning deep indigo-to-violet-black compound fruiting bodies. It forms a nutrient-sharing partnership with conifer tree roots and cannot be cultivated, making intact old-growth forest habitat essential to its survival. It has attracted significant scientific interest for a group of unique compounds called polyozellin and thelephoric acid derivatives with documented biological activity.

Polyozellus multiplex (Underw.) Murrill 1910 — Thelephoraceae — Thelephorales

Species P. multiplex
Family / Order Thelephoraceae / Thelephorales
Trophic Type Ectomycorrhizal
Defining Trait Deep indigo compound clusters
Range N. America + E. Asia
Season Late Aug – Oct

What Is the Blue Chanterelle (Polyozellus multiplex)?

Blue Chanterelle (Polyozellus multiplex) is one of the most visually distinctive mushrooms in North America — a compound, multi-capped fungus that emerges from the duff of old-growth spruce-fir forests in deep shades of indigo, violet, and near-black. Despite its common name and its chanterelle-like silhouette, it is not related to true chanterelles (Cantharellus spp.) at all. The resemblance is a case of convergent evolution: the same vase-and-ridge architecture evolved independently across unrelated lineages.

The Blue Chanterelle belongs to the order Thelephorales (the leathery earthfans, a group characterized by tough, pigment-rich fruitbodies and ectomycorrhizal ecology), family Thelephoraceae. Its closest relatives are the corticioid, crust-forming fungi in the genus Pseudotomentella — not chanterelles, and not black trumpets (Craterellus cornucopioides), with which it is sometimes confused in the field.

Interested in this species? Out-Grow carries a liquid culture.

Blue Chanterelle (Polyozellus multiplex) Liquid Culture

What makes Blue Chanterelle (Polyozellus multiplex) genuinely remarkable is the combination of features it packs into a single species: rare old-growth forest ecology, a documented pharmaceutical chemistry program spanning nearly three decades, use as a premium textile dye mushroom, and a recent discovery that it isn't even one species — it's five. That species-complex revelation, published in 2018, fundamentally changed what we know about this fungus and is still not reflected on most pages discussing it.

The single most important fact about Blue Chanterelle What the mycological community called "Polyozellus multiplex" for 119 years (1899–2018) turned out to be five distinct species. Most foraging records, field guide photos, and published chemistry studies cannot be retroactively assigned to any specific species without voucher DNA. When you read "blue chanterelle" anywhere before 2018, you're reading about an unresolved mixture of up to five different organisms.

How Is Blue Chanterelle (Polyozellus multiplex) Classified?

The taxonomy of Blue Chanterelle (Polyozellus multiplex) reflects more than a century of confusion. The species was first described in 1899 by Lucien Underwood as Cantharellus multiplex — placed with the chanterelles based on its vase-shaped fruitbody and forking hymenial ridges. William Alphonso Murrill moved it to the new genus Polyozellus in 1910 after recognizing its hyphal chemistry and spore morphology pointed elsewhere. The genus name derives from the Greek poly (many) and oz (branch), referring to the compound, many-branched growth form; multiplex means "manifold" in Latin, also describing this structure.

Subsequent recombinations into Craterellus (1938) and Thelephora (1954) reflected ongoing disagreement about its true affinities. Molecular phylogenetics ultimately resolved the question: Blue Chanterelle (Polyozellus multiplex) belongs firmly in Thelephorales, sister to the genus Pseudotomentella. A 2021 multi-gene analysis by Svantesson & Kõljalg further expanded the genus by recombining nearly all Pseudotomentella species into Polyozellus — transforming a genus of five stipitate species into one of roughly 25, mostly corticioid (crust-forming) species.

Rank Taxon
Kingdom Fungi
Phylum Basidiomycota
Subphylum Agaricomycotina
Class Agaricomycetes
Order Thelephorales
Family Thelephoraceae
Genus Polyozellus Murrill 1910
Species Polyozellus multiplex (Underw.) Murrill 1910

Synonyms and their origins: Cantharellus multiplex Underw. (1899, basionym); Craterellus multiplex (Underw.) Shope (1938); Thelephora multiplex (Underw.) A. Kawam. (1954). Obsolete names Murrillionum multiplex and Neurophyllum multiplex also appear in older literature. MycoBank ID: 124246.

The Species Complex — Five in One

A landmark 2017/2018 paper in Mycologia (Voitk, Saar, Trudell, Spirin, Beug & Kõljalg) demonstrated that the single morphological concept of "P. multiplex" comprised five molecularly and morphologically distinct species, four of them newly described. The split hinges partly on spore size — small-spored species (P. multiplex s.s. and P. atrolazulinus) versus large-spored species (P. mariae, P. marymargaretae, P. purpureoniger) — and partly on geographic range.

Species Spore Size Primary Range
P. multiplex s.s. Small (avg. 6.3 × 5.3 µm) Eastern N. America, East Asia
P. atrolazulinus Small (avg. 6.1 × 5.3 µm) Western N. America, Kuril Islands, NE N. America
P. mariae Large (avg. 8.3 × 7.0 µm) Eastern N. America (Newfoundland)
P. marymargaretae Large Washington State, Oregon
P. purpureoniger Large Alaska south to Washington, Russia, Kuril Islands

How Do You Identify Blue Chanterelle (Polyozellus multiplex)?

Blue Chanterelle (Polyozellus multiplex) is identified by a combination of habitat, macroscopic form, color chemistry, and — for confident species-level ID within the complex — spore measurements and DNA. No single macroscopic feature is diagnostic alone, but the full gestalt is unmistakable once seen.

Fruiting Body Size 15–30 cm across
Cap Width (Individual) 2–8 cm
Height 10–15 cm
Cap Color (Mature) Deep indigo to violet-black
Hymenium Color Pale grayish-violet (paler than cap)
Flesh Color Deep purple throughout (s.s.)
Spore Print White
KOH Reaction Blackish-green (diagnostic)
Spore Shape Subglobose, nodulose (warty)

The fruiting body is compound and multi-pileate (many-capped), with numerous fan-shaped to funnel-shaped individual caps arising from a shared fused base that is often partially subterranean. The cap surface is distinctly fuzzy or tomentose (woolly) in youth, becoming matte and smooth with age. Young growing tips show the most vivid color: pale gray-white to light violet-blue at the very margins, deepening to indigo-blue and violet-black toward the center. Dried specimens become brownish-gray to nearly black.

The hymenium (fertile undersurface) does not consist of true gills. It is formed by shallow, blunt longitudinal ridges that fork and anastomose (cross-connect), creating a veined or nearly poroid network — structurally similar to a chanterelle but consistently paler than the cap surface. A white spore dusting is often visible on mature specimens. The flesh is soft, brittle, deep purple throughout in P. multiplex s.s. — a key difference from P. mariae, which has straw-white to cream flesh.

The KOH test: Flesh treated with potassium hydroxide (KOH) turns distinctly blackish-green — this reaction is caused by the bluish-black wall pigment dissolving into an intensely colored solution. It is one of the most reliable field confirmation tools for this species and its relatives.

Lookalike Species

Caution — Toxic

Cortinarius violaceus (Violet Webcap)

Shares similar violet coloration but has true blade-like gills, a cobweb cortina (partial veil) when young, a rusty-brown spore print, and grows singly rather than in compound clusters.

Safe — Edible

Craterellus cornucopioides (Black Trumpet)

Dark coloring and funnel form are similar, but black trumpets are hollow and thin-walled, with a smooth to barely wrinkled outer surface and no blue-violet tones. Much smaller.

Safe — Edible

Laccaria amethystina (Amethyst Deceiver)

Has amethyst-violet tones but is far smaller, has distinct thin true gills, a white spore print, and grows as single fruitbodies rather than compound clusters.

Info — Edible

Gomphus clavatus (Pig's Ear)

Has decurrent ridges and a similar vein-like hymenium, but its cap is tan-brown to dull yellow-orange, and the growth form is more club-shaped. No blue tones.

Info — Variable

Thelephora spp.

Same family; dark coloring and leathery texture. Distinguished by a more openly fan-like or rosette growth form, no compound-cluster architecture, and no blue-violet tones.

Species complex ID caveat The two small-spored species — P. multiplex s.s. and P. atrolazulinus — cannot be reliably separated by macroscopic features alone. Spore measurements overlap significantly. Confident identification to species (not just genus) requires spore measurement and, ideally, multi-locus DNA sequencing. ITS alone is insufficient; RPB2 combined with nrLSU and nrSSU is the recommended marker combination.

Where Does Blue Chanterelle (Polyozellus multiplex) Grow?

Blue Chanterelle (Polyozellus multiplex) is an obligate ectomycorrhizal (ECM) fungus — one that forms a mutually beneficial symbiosis exclusively with living tree roots. In ectomycorrhiza, fungal hyphae form a dense sheath (mantle) around fine roots and penetrate between (but not into) the root cortex cells, creating the Hartig net. The fungus delivers water and mineral nutrients (especially phosphorus and nitrogen) to the tree; the tree transfers photosynthetically fixed carbon back to the fungus. Neither organism can thrive without the other.

Primary documented host trees are Picea spp. (spruce) — including Sitka spruce (P. sitchensis), black spruce (P. mariana), and red spruce (P. rubens) — and Abies spp. (fir), including balsam fir (A. balsamea) and subalpine fir (A. lasiocarpa). Blue Chanterelle (Polyozellus multiplex) consistently associates with mature and old-growth stands; it is not documented from young plantations or recently disturbed forest.

Region Specific Range Peak Season
Pacific Northwest Alaska south through British Columbia, Washington, Oregon into northern California; Cascade and Coast Ranges. Likely mostly P. atrolazulinus + P. marymargaretae/purpureoniger. September–October
Eastern N. America Maine, Vermont, New Hampshire, New York, Quebec, New Brunswick, Nova Scotia, Newfoundland, south to North Carolina. P. multiplex s.s. and P. mariae. Late August–October
Japan Yamanashi Prefecture and elsewhere; commercially harvested (known as Kurokawa) Early autumn
Korea Widely distributed; significant commercial and scientific interest Late August–October
China Southern and eastern provinces; sold at markets (e.g. Yunnan) Autumn
Kuril Islands Documented; P. atrolazulinus and P. purpureoniger Autumn

Fruiting is erratic and unpredictable. Individual sites may produce for a decade and then skip years unpredictably. Reports from Newfoundland suggest some sites fruit only every 5 to 20 years, with many lifelong local foragers never encountering the species. This irregularity, combined with its old-growth habitat requirement, makes Blue Chanterelle (Polyozellus multiplex) genuinely rare in the field.

Microhabitat preferences are consistent across the range: sandy or loamy soils with conifer duff and moss, often among fruticose lichens; low, wet spruce-fir forests, as well as higher-elevation subalpine stands. Blue Chanterelle (Polyozellus multiplex) is recognized by the USDA Forest Service as a Survey & Manage species under the Northwest Forest Plan — a protection category for uncommon or old-growth-associated fungi on federal lands in the range of the northern spotted owl.

Can You Cultivate Blue Chanterelle (Polyozellus multiplex)?

This is the question every prospective cultivator asks, and it deserves a complete and honest answer. Blue Chanterelle (Polyozellus multiplex) is an obligate ectomycorrhizal fungus. This one biological fact shapes everything that follows.

Ectomycorrhizal fungi are biochemically dependent on photosynthetically fixed sugars from a living host tree. Unlike saprotrophic mushrooms — oysters, shiitakes, lion's mane — they cannot feed themselves by decomposing dead organic carbon. Without the carbon stream from a living Picea or Abies partner, the mycelium either grows extremely slowly or stops growing entirely. Fruiting body formation outside of the mycorrhizal relationship is biologically impossible. No peer-reviewed study has produced Blue Chanterelle (Polyozellus multiplex) fruiting bodies under controlled conditions. This is the honest baseline.

How does this compare to other ECM mushrooms? Cantharellus anzutake (Japanese yellow chanterelle) is the only chanterelle species for which controlled fruiting has been achieved — it required full mycorrhizal synthesis with pine and oak seedlings, years of careful lab work, and conditions that are beyond typical hobbyist setups. Matsutake (Tricholoma matsutake), despite enormous commercial investment, has never been fruited under controlled conditions. Blue Chanterelle presents the same class of challenge.

What the Liquid Culture Is — and What It Isn't

A liquid culture of P. multiplex mycelium is living fungal tissue preserved in aqueous growth medium. Out-Grow's mycology lab has observed the mycelium growing as white, fine, wispy colonies with low-to-moderate density on malt extract agar (MEA), colonizing a 100mm plate in approximately 14–28 days at 55–64°F — slow growth consistent with its ECM ecology.

What Out-Grow's Blue Chanterelle Culture Is For

Out-Grow's Blue Chanterelle (Polyozellus multiplex) liquid culture contains living mycelium of this rare old-growth forest fungus. Its most scientifically supported applications are research and experimental work — not conventional cultivation in grain jars or grow bags, which is not consistent with this species' obligate ECM biology.

Realistic uses include: (1) Research and biochemistry — mycelium-based production of the documented bioactive compounds (polyozellin, kynapcins, thelephoric acid) for laboratory study; (2) Agar and culture work — inoculating MEA plates for colony observation, genetic voucher creation, or culture multiplication; (3) Experimental host-tree inoculation — applying liquid culture mycelium to sterilized root systems of Picea or Abies seedlings as inoculum for mycorrhizal synthesis research, following the protocols developed for chanterelle and matsutake research. This is the closest currently available pathway toward any future fruiting body production. Liquid culture stored cool and dark maintains viability for culture transfer and experimental work.

Experimental Host-Tree Inoculation Pathway

For researchers interested in pursuing the mycorrhizal route, the pathway informed by analogous ECM work would proceed through these stages:

1

Pure Culture Establishment

Isolate from fruiting body tissue under sterile conditions. Hydrogen peroxide agar or antibiotic-supplemented media may improve success by suppressing bacterial contamination, as documented in chanterelle research.

2

Expansion on ECM Media

Expand culture on Modified Melin-Norkrans (MMN) agar — formulated for ECM fungi with low glucose (1%), mineral salts, and vitamins. Expect slow growth; ECM species grow at a fraction of saprotrophic rates.

3

Seedling Inoculation

Apply culture to roots of Picea or Abies seedlings (sterilized root systems in growth pouches with low-phosphorus sterile substrate). Confirm ECM formation by examination of root tip morphology.

4

Outplanting

Establish mycorrhizal seedlings in field conditions under mature compatible hosts. Years of establishment would be required before fruiting could theoretically occur. No specific timeline data exists for Polyozellus.

Mycelium Temp (Optimal) 55–64°F (13–18°C)
Humidity 90–95%
Preferred Media MMN agar or MEA
Plate Colonization 14–28 days
Contam Sensitivity Moderate — clean technique critical
Fruiting (Conventional) Not documented

What Bioactive Compounds Does Blue Chanterelle (Polyozellus multiplex) Contain?

Blue Chanterelle (Polyozellus multiplex) has been the subject of a productive research program primarily from Korean and Japanese laboratories since the mid-1990s. The chemical profile is exceptional among edible mushrooms — dominated by benzofuran dimers (the kynapcin series), p-terphenyl compounds (polyozellic acid, thelephoric acid), and dibenzofuran derivatives (polyozellin). All published studies used wild-collected Korean or Japanese fruiting bodies from before the 2018 species-complex split, so the specific species contributing to each result cannot be confirmed retroactively.

Polyozellin

Dibenzofuran Derivative · CAS 197703-46-1

First isolated as a prolyl endopeptidase (PEP) inhibitor (Hwang et al. 1997). PEP is a serine protease that cleaves proline-containing neuropeptides including vasopressin and substance P; its activity is elevated in Alzheimer's disease. Polyozellin also induces Phase 2 detoxification enzymes (quinone reductase, glutathione S-transferase) in mouse hepatoma cells; suppresses NF-κB and SAPK/JNK activation in LPS-stimulated macrophages; and protects mouse hippocampal neurons (HT22 cells) from glutamate-induced death at 25 µM.

In vitro + mouse models

Kynapcin-28

Benzofuran Dimer

Most potent of the kynapcin PEP inhibitors. IC₅₀ = 0.98 µM — noncompetitive inhibition with high selectivity over chymotrypsin, trypsin, and elastase. Isolated by Kim et al. (2002) in Journal of Antibiotics.

In vitro

Kynapcin-24

Benzofuran Dimer

Noncompetitive PEP inhibitor; IC₅₀ = 1.14 µM. Structure confirmed by Song et al. (2002) in Journal of Natural Products. High selectivity over other serine proteases.

In vitro

Kynapcin-13

Benzofuran

Noncompetitive PEP inhibitor; IC₅₀ = 76.80 µM. Less potent than the dimer forms but part of the same series. Isolated alongside kynapcin-28 by Kim et al. (2002).

In vitro

Polyozellic Acid

p-Terphenyl (o-Quinone) · Novel

Anti-angiogenesis activity — inhibits proliferation, tubule formation, and invasion of human umbilical vein endothelial cells (HUVECs). The o-quinone moiety is proposed as the pharmacophore. Structure confirmed by X-ray crystallography (Nagasawa et al. 2014, J. Nat. Prod.).

In vitro

Thelephoric Acid

p-Terphenyl Quinone Pigment

The principal pigment of Thelephoraceae broadly. Also anti-angiogenic against HUVECs alongside polyozellic acid. Responsible for the characteristic indigo-to-black coloration of the fruitbody and the deep grey-to-black textile dye the species yields. Isolated from Japanese collections (Nagasawa et al. 2014).

In vitro
Evidence quality — important caveat Every pharmacological study on Blue Chanterelle (Polyozellus multiplex) to date is either in vitro (cell culture) or animal model (mouse). No randomized controlled trials or human clinical studies have been published for any P. multiplex-derived compound. In vitro activity does not translate directly to clinical efficacy. The PEP inhibition data are the most developed line of evidence and represent a rationally supported direction for future clinical investigation — but human evidence does not yet exist.

Is Blue Chanterelle (Polyozellus multiplex) Safe to Eat?

Blue Chanterelle (Polyozellus multiplex) has a longstanding record as an edible mushroom in Korea, Japan, China, and North America. No specific toxic compounds have been identified in this species, and no cases of poisoning specifically attributable to P. multiplex s.l. appear in the North American mushroom poisoning literature or in clinical toxicology databases. In East Asian markets it is sold commercially during autumn seasons; it is considered choice-quality in Korea and Japan, prized for its firm, meaty texture.

Three important caveats apply. First, the species is uncommon to rare across its range, meaning the consumption volume is low enough that even a low-frequency adverse reaction might not generate reportable case numbers. Second, the 2018 species-complex split means that consumers historically eating "blue chanterelle" may have been consuming any of five species, with potentially different chemical profiles; safety assessments do not exist specifically for the newly described species. Third, the bioactive compounds present — particularly thelephoric acid as a quinone and polyozellin as a dibenzofuran — are pharmacologically active at relevant concentrations in cell assays, and the safety of chronic consumption at food quantities has not been formally assessed in humans.

Standard wild mushroom precautions apply: accurate identification (the KOH test is helpful), moderate initial serving, do not consume raw in large quantities. No specific drug interactions are documented, though individuals on anticoagulants, immunosuppressants, or anti-inflammatory medications might exercise caution given polyozellin's demonstrated effects on NF-κB and related pathways in cell studies.

What Makes Blue Chanterelle (Polyozellus multiplex) Remarkable?

119 Years Hidden as One Species

The species-complex discovery began not in a lab but in the field, when Maria Voitk insisted that a Gros Morne National Park specimen was "a Polyozellus, but not the usual one" — against her mycologist husband's certainty that no other species existed. The nine-year process from field observation (2009) to publication (2018) resulted in four new species described. Most online content still describes the genus as monotypic (containing only one species).

A Premium Textile Dye Mushroom

Blue Chanterelle (Polyozellus multiplex) is valued by natural dyers as a reliable source of blue-grey, dark grey, and near-black dyes for protein fibers (wool, silk). Thelephoric acid and related p-terphenyl pigments form stable metal-ligand complexes with mordant fibers. An alum mordant yields grey-violet tones; iron yields near-black. This is a significant and historically established use almost entirely absent from mycological species guides.

Exceptional Fruiting Body Persistence

The resistance of Blue Chanterelle (Polyozellus multiplex) fruiting bodies to decay and invertebrate damage is unusual — field persistence of over a month has been documented. The only significant predators are slugs, which can destroy entire clusters. The mechanism of decay resistance is undocumented but may relate to the presence of pharmacologically active secondary metabolites.

Disjunct North America – East Asia Distribution

The occurrence pattern — boreal and montane North America plus East Asia, absent from Europe — mirrors numerous other fungal and plant taxa reflecting Beringian biogeographic connections. The 2018 paper flagged that multilocus analysis may ultimately show Asian and North American populations of P. multiplex s.s. have diverged into separate species — an unresolved question.

An Unusual Chemical Toolkit

The combination of benzofuran dimers (kynapcin series), p-terphenyl compounds (polyozellic acid, thelephoric acid), and dibenzofuran derivatives (polyozellin) in a single edible mushroom is exceptional. The structural diversity of PEP inhibitors discovered in this one species is remarkable, and the p-terphenyl class — while shared across Thelephoraceae — reaches unusual complexity here.

Old-Growth Forest Indicator

Blue Chanterelle (Polyozellus multiplex) is recognized as an indicator species for old-growth forest quality in the Pacific Northwest. Its presence signals mature, undisturbed forest with intact ECM networks — networks that are directly threatened by logging of old-growth spruce-fir stands. USDA Northwest Forest Plan Survey & Manage protections represent its primary regulatory shield on federal lands.

Frequently Asked Questions About Blue Chanterelle (Polyozellus multiplex)

Is Blue Chanterelle (Polyozellus multiplex) really a chanterelle?

No — despite the common name and a similar vase-and-ridge form, Blue Chanterelle (Polyozellus multiplex) is not related to true chanterelles (Cantharellus spp.). It belongs to the order Thelephorales, family Thelephoraceae, and is more closely related to the corticioid crust fungi of the genus Pseudotomentella. The resemblance to chanterelles is convergent evolution — the same form arising independently in unrelated lineages that share similar habitats and ecological roles.

Can Blue Chanterelle (Polyozellus multiplex) be cultivated at home?

Conventional home cultivation on grain, straw, or compost is not possible. Blue Chanterelle (Polyozellus multiplex) is an obligate ectomycorrhizal fungus that requires a living Picea or Abies tree partner to complete its life cycle. No fruiting body production has been documented under controlled conditions in peer-reviewed literature. A liquid culture can be used for research, agar work, and experimental host-tree seedling inoculation — the closest currently available path toward any future cultivation.

How many species are in the Blue Chanterelle complex?

Five. The 2017/2018 Voitk et al. paper in Mycologia showed that the single morphological concept of "Polyozellus multiplex" comprised five molecularly distinct species: P. multiplex s.s., P. atrolazulinus, P. mariae, P. marymargaretae, and P. purpureoniger. Most foraging records and published chemistry studies before 2018 cannot be assigned to a specific species without voucher DNA.

Is Blue Chanterelle (Polyozellus multiplex) edible?

Yes — it has a longstanding record of safe consumption in Korea, Japan, China, and North America, and is considered choice-quality in East Asian markets. No toxic compounds have been identified and no poisoning cases are documented in the literature. Standard wild mushroom precautions apply: accurate identification (the KOH reaction test is useful), moderate initial serving, do not eat raw in large quantities. The 2018 species split means that historical safety records cover the whole complex, and safety assessments do not exist specifically for the newly described species.

What is polyozellin and why does it matter?

Polyozellin is a dibenzofuran compound isolated from Blue Chanterelle (Polyozellus multiplex) fruiting bodies, first characterized as a prolyl endopeptidase (PEP) inhibitor in 1997. PEP is a serine protease that cleaves neuropeptides and is elevated in Alzheimer's disease. Subsequent studies showed polyozellin also induces cellular detoxification enzymes, suppresses inflammatory NF-κB signaling, and protects hippocampal neurons from glutamate-induced death in cell culture. All evidence is in vitro or animal-model; no human clinical trials exist. It remains a pharmacologically active compound under active investigation.

Where does Blue Chanterelle (Polyozellus multiplex) grow?

Blue Chanterelle (Polyozellus multiplex) grows in old-growth and mature coniferous forests under spruce (Picea) and fir (Abies) trees. Its range spans northern and montane North America (Pacific Northwest, Rocky Mountains, eastern Canada and northeastern US) and East Asia (Japan, Korea, China). It is absent from Europe. Fruiting is erratic — some sites produce reliably for years, others skip decades. Peak season is late August through October depending on latitude and elevation.

Also available as a culture plate from Out-Grow.

Blue Chanterelle (Polyozellus multiplex) Culture Plate