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Ganoderma tsugae

Ganoderma tsugae Species Guide

Ganoderma tsugae

Ganoderma tsugae is a lacquered, shelf-forming fungus native to the hemlock forests of eastern North America and Northeast China, recognized instantly by its glossy mahogany cap and pure. It holds a distinct place in both mycology and traditional medicine as the conifer-specialist cousin of the famous reishi, producing documented bioactive polysaccharides and lanostane triterpenoids with a growing body of preclinical research. Unlike most laccate Ganoderma species, it thrives on conifer wood—an adaptation written into its genome—and can be cultivated on log and sawdust substrates for both hobbyist and research purposes.

Ganoderma tsugae Murrill — Family Ganodermataceae — Order Polyporales

Species Ganoderma tsugae
Family / Order Ganodermataceae / Polyporales
Type White-rot bracket fungus
Defining Trait Laccate cap; pure white flesh
Range Eastern N. America; NE China; Taiwan
Season Spring through fall (May–Oct)

Ganoderma tsugae is one of North America’s most visually striking wood-decay fungi—a varnished, shelf-forming bracket mushroom that emerges from dying and dead hemlock trees each spring like a lacquered sculpture. It was formally described in 1902 by mycologist William Alphonso Murrill from specimens collected on eastern hemlock (Tsuga canadensis), and decades of molecular work have since confirmed it as a species distinct from the Asian reishi of traditional medicine. Cultivated commercially in Taiwan and Northeast China and studied in peer-reviewed research for its polysaccharides, lanostane triterpenoids, and unusual genomic adaptations to coniferous wood, Ganoderma tsugae is genuinely one of the most scientifically interesting fungi in temperate North America.

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

Ganoderma tsugae Liquid Culture

What Is Ganoderma tsugae?

Ganoderma tsugae is a bracket fungus—a polypore (pore-bearing fungus) that grows as a shelf or fan projecting from the wood of its host tree rather than as a capped, gilled mushroom. The defining visual feature is the laccate surface: the cap appears as though it has been coated in high-gloss lacquer or varnish, cycling through white, bright yellow-orange, and deep reddish-mahogany as the fruiting body matures. Beneath that glossy crust, the flesh is pure white and, when fresh, moderately soft—a key identification character that distinguishes it from hardwood-associated lookalikes whose flesh is buff or tan.

The common name “Hemlock Reishi” signals both its host preference and its relationship to the famous reishi of East Asian medicine. In the field guide tradition, the species is also known as the hemlock varnish shelf—a name that emphasizes the lacquered appearance and conifer association. In Taiwan, where it is commercially cultivated, it is sold under the umbrella of Lingzhi.

Key Fact

Despite carrying the “reishi” name, Ganoderma tsugae is not the same species as the reishi of traditional Chinese medicine (G. lucidum or G. lingzhi). Molecular phylogenetics confirms they are distinct species with related but non-identical triterpenoid and polysaccharide profiles—extrapolating health claims directly from one to the other is scientifically unwarranted.

Ecologically, Ganoderma tsugae functions as both a saprobe (decomposer of dead wood) and a weak parasite on living trees. As a saprobe, it breaks down cellulose, hemicellulose, and lignin through white rot—a process that leaves wood pale, fibrous, and spongy rather than the brown and crumbly result of brown rot. As a weak parasite, it can colonize the heartwood of living hemlocks through root wounds and mechanical damage, causing a structural butt rot that may take years to kill the host. This dual role has real implications for cultivation: because G. tsugae is a lignicolous (wood-dependent) saprobe, not a mycorrhizal fungus (one requiring a living tree partner), it can be cultivated on logs and wood-based substrates without a living host tree.

How Is Ganoderma tsugae Classified?

Rank Name
Kingdom Fungi
Phylum Basidiomycota
Subphylum Agaricomycotina
Class Agaricomycetes
Order Polyporales
Family Ganodermataceae
Genus Ganoderma P. Karst.
Species Ganoderma tsugae Murrill
MycoBank ID MB#239416

William Alphonso Murrill described Ganoderma tsugae in 1902 in the Bulletin of the Torrey Botanical Club, from specimens collected on eastern hemlock in the northeastern United States. The species name tsugae is the genitive form of Tsuga—Latin for “of the hemlock.” Early 20th-century mycologists including Atkinson proposed that G. tsugae was simply a North American form of the European G. lucidum, lumping all shiny-capped Ganoderma together. Overholts disagreed and maintained the species, and a pivotal 2018 multilocus molecular study by Loyd and colleagues, analyzing over 500 North American Ganoderma collections using four genetic markers (ITS, tef1α, rpb1, rpb2), vindicated that judgment conclusively.

The Loyd et al. study placed G. tsugae as the sister taxon (closest relative) of G. oregonense—a western North American conifer specialist—in a well-supported clade entirely separate from the hardwood-associated North American Ganoderma species and from Old World reishi. The family Ganodermataceae, rather than the older placement in Polyporaceae, is the current scientific consensus, supported by the distinctive double-walled basidiospores (reproductive spores) with interwall pillars that are unique to this family.

Nomenclature Note

NCBI Taxonomy lists Polyporus tsugae as the “current name”—this reflects a known database discrepancy, not scientific authority. Index Fungorum and MycoBank, the authoritative nomenclatural resources, accept Ganoderma tsugae Murrill as the valid name. The synonym Polyporus tsugae (Murrill) Overh. dates from a 1915 generic transfer that is no longer followed.

How Do You Identify Ganoderma tsugae?

The most immediate recognition character for Ganoderma tsugae is the combination of glossy, lacquer-like cap surface and white context (flesh). Young specimens display a striking developmental color progression: the growing margin and newest tissue are white or cream, shading through bright yellow and orange toward the older central tissue, which matures to reddish-orange, reddish-brown, or dark mahogany. Old or weathered specimens often become coated in a thick layer of brown spores that temporarily obscures the varnish.

Cap Width
4–20 (30) cm
Cap Shape
Fan-shaped to kidney-shaped; laccate
Cap Color
White → orange → mahogany
Flesh Color
Pure white; azonate
Pore Surface
White when fresh; bruises brown; 4–6 pores/mm
Stem (Stipe)
3–14 cm; lateral; varnished
Spore Print
Brown
Spore Size
8–12 × 5–7 µm (outer wall); double-walled
KOH Reaction
Flesh instantly turns black
Hyphal System
Trimitic (generative, skeletal, binding hyphae)

The KOH reaction—a drop of 5–10% potassium hydroxide solution turns the flesh and tube layer instantly black—is a consistent, diagnostically useful feature across all laccate Ganoderma. The trimitic (three-type) hyphal system (visible under a microscope) and the presence of clamp connections (microscopic loop-like structures on generative hyphae) are confirming microscopic features. The double-walled basidiospores with interwall pillars are characteristic of the family Ganodermataceae as a whole.

Lookalike Species

Ganoderma sessile

Grows on hardwoods (oaks, maples), never on hemlock. Flesh is buff to tan, not white. Often sessile (no stem) or very short-stemmed. Melanoid bands (dark concentric zones) sometimes present in flesh. Most likely confusion in eastern North America.

Ganoderma curtisii

Hardwood-associated; often has a dramatically elongated lateral stem. Flesh is buff-cinnamon, not white. Melanoid bands sometimes present. Geographic range overlaps with G. tsugae in eastern North America.

Ganoderma oregonense

The sister taxon of G. tsugae; grows on conifers in western North America. White flesh, absent melanoid bands, and similar morphology. ITS barcoding alone cannot reliably separate these two species—multilocus molecular analysis is required for specimens from western states.

Ganoderma applanatum

The “artist’s conk.” Easily separated: the upper surface is matte gray-brown with NO lacquer or varnish. Grows on hardwoods and conifers. The absence of any glossy finish makes this one of the simplest distinguishing features in mycology.

Ganoderma lucidum s.s.

True G. lucidum sensu stricto is essentially absent from wild eastern North American populations—it grows primarily on hardwoods in Europe and has only geographically limited North American records. Any laccate Ganoderma found on hemlock in the eastern US is almost certainly G. tsugae.

Critical ID Pitfall

In the Pacific Northwest, the conifer-associated laccate Ganoderma is G. oregonense, not G. tsugae. These sister species are morphologically very similar and share overlapping ITS sequences. If you are sourcing cultures for cultivation or research and authenticity matters, request multilocus molecular verification or ITS + tef1α barcoding.

Where Does Ganoderma tsugae Grow?

Ganoderma tsugae has a distribution anchored to the range of eastern hemlock (Tsuga canadensis) in North America. In its primary range, it occurs from Nova Scotia south through New England, across the Great Lakes region, down the spine of the Appalachian Mountains, and into the Gulf Coast areas where hemlock persists. Outlying records exist from Arizona and New Mexico. In eastern North America, the species grows almost exclusively on eastern hemlock and, less commonly, Carolina hemlock (T. caroliniana)—a degree of substrate specificity unusual even by Ganoderma standards.

Region Substrate Status
Eastern North America Tsuga canadensis (eastern hemlock); rarely T. caroliniana Wild; primary range
Pacific Northwest / Rockies Conifer records rare; most conifer-associated laccate Ganoderma here is G. oregonense Marginal / misidentified
Northeast China (Changbai Mt.) Larch (Larix gmelinii), firs (Abies spp.) Wild and cultivated; research center
Taiwan Cultivated commercially on various substrates Dominant cultivated Ganoderma

Fruiting bodies develop from spring through fall in eastern North America, typically beginning in May or June and continuing through October. They are annual—meaning a new fruiting body forms each season, unlike the perennial brackets of G. applanatum (artist’s conk), though old woody tissue may persist through winter. Fruiting bodies appear on dead standing snags, stumps, fallen logs, and occasionally at the base of living trees where heartwood infection has taken hold.

Ecological Alert

The hemlock woolly adelgid (Adelges tsugae), an invasive insect from Asia, is causing widespread mortality of eastern hemlock across the Appalachian Mountains and New England. This creates an ecological paradox: in the short term, dying hemlocks generate an unprecedented abundance of fresh substrate, and foragers in adelgid-affected areas have noted increased G. tsugae fruiting. In the long term, if eastern hemlock is lost from the landscape, the primary substrate for Ganoderma tsugae in eastern North America disappears with it. No formal conservation assessment has been published for this species in the context of hemlock woolly adelgid mortality.

Can You Cultivate Ganoderma tsugae?

Yes. Ganoderma tsugae is a cultivated fungus. Because it is saprotrophic—obtaining nutrition by decomposing dead wood—rather than mycorrhizal (dependent on a living tree partner), it can be grown on appropriate lignocellulosic (wood-based) substrates without a living host. Commercial production is established in Northeast China (primarily on larch logs) and Taiwan. North American hobbyist and small-farm cultivation on logs and supplemented sawdust is documented, though specific biological efficiency data for sawdust cultivation has not been published in peer-reviewed literature.

Log Cultivation (Peer-Reviewed Data)

The most current peer-reviewed cultivation study (Xia et al. 2024, published in Life) evaluated larch wood inoculation with G. tsugae strain HLXL1 under a pine forest canopy. A particularly practical finding: non-sterilized larch logs produced marginally superior results compared to sterilized logs, and both cultivated groups significantly outperformed wild controls in fruiting body yield and bioactive compound content. This suggests that log cultivation does not require energy-intensive sterilization, mirroring traditional shiitake log cultivation practices.

1

Substrate Preparation

Larch, hemlock, or other conifer logs or sawdust. Non-sterilized larch logs perform as well as sterilized in outdoor settings (Xia et al. 2024). Supplement sawdust blocks with wheat bran, rice bran, or soy hulls per G. lucidum protocols (hobbyist-reported; not peer-reviewed for G. tsugae specifically).

2

Inoculation

Inject liquid culture into sterilized grain or pre-drilled log holes via plug spawn. Liquid culture (LC) inoculant gives faster colonization than spore-based inoculants. Store LC syringes refrigerated (not frozen) until use.

3

Spawn Run

Optimal temperature: 25–28°C (77–82°F). Colonization is slow compared to aggressive edible species—allow adequate time and maintain strict contamination control. Trichoderma spp. (green mold) is the primary contamination risk on improperly sterilized substrate.

4

Fruiting Conditions

Humidity 90–95%; temperatures 21–24°C (70–75°F) for fruiting (vendor-reported). Fruiting trigger conditions (temperature drop, CO₂ level, FAE—fresh air exchange) are not formally characterized in peer-reviewed literature for this species—an open research gap. Increase fresh air exchange to stimulate pinning.

5

Harvest & Timing

Harvest fruiting bodies when the white growing margin begins to recede and the pore surface starts darkening. For bioactive compound production, mineral content and compound concentrations vary significantly across developmental stages (Xia et al. 2024).

6

Contamination Control

Slow colonization makes G. tsugae vulnerable to fast-growing contaminants, especially Trichoderma spp. Use alcohol-sterilized transfer surfaces, still-air box or flow hood for agar work, and rigorous substrate sterilization. Bacterial contamination in liquid fermentation requires monitoring (Phenol Red Broth and TSA plate purity checks recommended).

What Is the Ganoderma tsugae Liquid Culture?

A liquid culture (LC) is a suspension of live Ganoderma tsugae mycelium in a sterile nutrient solution, contained in a syringe for easy inoculation. It is the most efficient transfer method for introducing this species to a new substrate—grain jars, supplemented sawdust bags, or pre-drilled log holes—because the mycelium is already metabolically active and colonization begins immediately on injection.

In published submerged fermentation research (Serody et al. 2024), G. tsugae in liquid culture forms circular, spider-like pellets, reaches peak biomass of 11.4 g/L at Day 3, and produces exopolysaccharides (EPS) at 1.68 g/L under optimized conditions—exceeding G. lucidum under comparable protocols. The LC can also be used to generate mycelial biomass directly for research and nutraceutical applications, independent of fruiting body production.

Out-Grow’s liquid culture syringe is refrigerated until use and remains viable for months when stored correctly. Optimal carbon source for submerged culture is lactose at 20 g/L; optimal temperature 28°C; optimal pH 5.5; optimal agitation 120 rpm (above 150 rpm causes pellet shearing damage).

What Bioactive Compounds Does Ganoderma tsugae Contain?

Ganoderma tsugae contains two primary bioactive compound classes: polysaccharides and lanostane-type triterpenoids. Both have been structurally characterized from G. tsugae specifically in peer-reviewed research—not extrapolated from G. lucidum—and both show bioactivity in in vitro and animal model studies. Evidence quality is assessed honestly for each claim below.

Fucogalactan (GTP-a2)

A polysaccharide isolated from G. tsugae fruiting bodies (MW = 7.056 kDa; backbone of →6α-D-Galp1→ with L-fucose branches). Demonstrated anti-colorectal cancer activity in a mouse colitis-associated cancer model, modulating the mTOR/PI3K/AKT signaling pathway and preventing M1 macrophage polarization. Zhang et al. 2025, Carbohydrate Polymers.

Animal model
Exopolysaccharides (EPS)

Produced at 1.68 g/L peak under optimized liquid fermentation conditions—higher output than G. lucidum under comparable conditions. EPS from related species show antioxidant and immunomodulatory activity in vitro. The unusual use of lactose as optimal carbon source (not shared by G. lucidum) has commercial fermentation implications.

In vitro
Antioxidant Phenolics

Hot-water extracts of mature G. tsugae fruiting bodies show DPPH scavenging at 78.5% at 20 mg/mL, and EC₅₀ (reducing power) of 1.08 mg/mL. Mycelium extracts showed even higher scavenging (~91.2% DPPH). Total phenolics: ~4.1–6.3 mg gallic acid equivalents (GAE)/g dry weight. Mau et al. 2005, LWT Food Science.

In vitro
Tsugaric Acid C & Tsugarioside B/C

Novel lanostanoid triterpenoids isolated specifically from G. tsugae fruiting bodies; cytotoxic activity against cancer cell lines evaluated. First published isolation of G. tsugae-specific triterpenoids. Su et al. 2000, Journal of Natural Products.

In vitro
Antibacterial Lanostane Triterpenoids

Lanostane triterpenoids isolated from fruiting bodies showing antibacterial activity against Corynebacterium CRM197, Enterococcus sp. MB2-1, and E. faecalis ATCC 10132 in vitro. A structural HMG group (rather than MeHMG) is required for activity. Hu et al. 2023/2024, Journal of Asian Natural Products Research.

In vitro
Platycodigenin, Cucurbitacin IIb, Ganolecidic Acid B

Three triterpenoids structurally identified by high-resolution mass spectrometry from rice solid-state fermentation of G. tsugae strain G42 (total triterpenoid yield: 53.86 mg/g). Ethanol extract from this fermentation showed hepatoprotective activity in a CCl₄-induced liver injury mouse model. Zhang et al. 2022, Molecules.

Animal model
Evidence Quality Flag

All bioactive compound characterization for Ganoderma tsugae is from in vitro (cell culture) or animal model studies. No randomized controlled trials or other controlled human studies have been published specifically for G. tsugae as of March 2026. EC₅₀ values from cell assays are concentrations in culture medium—not human bioavailable doses. Evidence from G. lucidum human trials cannot be directly transferred to G. tsugae.

Is Ganoderma tsugae Safe to Eat?

Ganoderma tsugae is not a culinary mushroom mushroom in the conventional sense—the flesh of mature specimens is tough, woody, and intensely bitter. Young specimens with white, soft flesh are sometimes consumed in small quantities, particularly in Taiwan and Northeast China, but the species is primarily used as a dried extract rather than a fresh food. No specific toxic compounds have been documented for G. tsugae, and no published case reports of acute or chronic toxicity from consumption were found in the literature reviewed for this guide.

In a preclinical safety evaluation, Yu et al. (2012) administered G. tsugae ethanol extract to tumor-bearing nude mice at 100 mg/kg/day orally for 45 days; pathological examination of major organs showed no significant evidence of hemorrhage, necrosis, or inflammation compared to controls. The absence of documented toxicity is meaningful, particularly given the widespread traditional use in Taiwan over decades, but should not be read as confirmed human safety—systematic long-term toxicology studies specific to G. tsugae have not been conducted.

Cautions

Anticoagulant interaction: Ganoderma species broadly exhibit anticoagulant and antiplatelet effects. Individuals on blood-thinning medications (warfarin, aspirin, clopidogrel) should consult a physician before use. Pregnancy and nursing: No safety data exists for G. tsugae in pregnancy or lactation. Spore inhalation: Old sporulating specimens release large quantities of brown spores; respiratory protection is advisable when harvesting heavily sporulating material in enclosed spaces. Supplement quality: Products labeled as reishi or Ganoderma in the supplement industry have significant mislabeling rates; ITS barcoding of commercial products frequently reveals species substitution.

What Makes Ganoderma tsugae Remarkable?

Several features of Ganoderma tsugae place it among the scientifically most interesting temperate fungi—not just as a medicinal species, but as a subject of evolutionary biology, mycology, and ecology.

Genomic Adaptation to Conifer Wood

Most laccate Ganoderma grow on hardwoods. Conifer wood is saturated with terpenes, phenolics, and antimicrobial resin compounds that would inhibit or kill most fungi. The 2021 whole-genome study (Jiang et al., Frontiers in Microbiology) reveals the mechanism: G. tsugae has evolved an expanded toolkit of detoxification enzymes—salicylate hydroxylase, phenol monooxygenase, benzoate-degrading cytochromes P450—and an expanded DNA repair pathway (Fanconi anemia/homologous recombination genes) to counteract the DNA-damaging effects of conifer chemicals. This is a documented case of fungal genomic adaptation to a chemically hostile substrate.

Laccase as the Color Switch

The laccase gene Lcc1 (GenBank KT166425.1) is not just a wood-degrading enzyme in G. tsugae—it is the genetic switch controlling the species’ defining visual feature. Gene knockout experiments show that ΔLcc1 mutants produce sparse mycelium and generate small, pale grey fruiting bodies entirely lacking the characteristic dark red laccate cap. Lcc1 expression follows a biphasic pattern: high during mycelium development (Stage I), dramatically downregulated at primordium and stipe stages (Stages II–III), then surging 20.5-fold at fruiting body maturation (Stage IV). The red lacquer cap that makes this species unmistakable in the field is directly dependent on this single gene’s expression.

Lactose Metabolism—A Fermentation Curiosity

Unlike G. lucidum, Ganoderma tsugae utilizes lactose as a primary carbon source for both biomass and EPS production in submerged fermentation—and actually performs better on lactose than on glucose. Lactose is a dairy industry waste product available at very low cost. This metabolic trait makes G. tsugae potentially more economical than G. lucidum for large-scale bioreactor production of mycelial biomass and exopolysaccharides, and opens an interesting research question about the genetic basis of unusual carbohydrate utilization in wood-rot fungi.

Wild and Cultivated Strains Genetically Identical

Population genomics of 22 G. tsugae strains found no genetic separation between wild and cultivated populations—they form a single cluster in phylogenetic and principal component analyses. In most domesticated fungi and agricultural organisms, cultivation quickly imposes measurable genetic divergence from wild populations. The indistinguishable genetic backgrounds of wild and cultivated G. tsugae imply either very recent domestication or active gene flow between cultivated and wild populations—an unusual finding with implications for understanding fungal domestication more broadly.

Divergence and Paleoclimate

The G. tsugae lineage diverged from the ancestor of G. lingzhi, G. sinense, and G. boninense approximately 21 million years ago—a divergence that coincides temporally with the early Himalayan orogeny, which fundamentally altered precipitation, temperature, and vegetation across Eurasia. The formation of conifer-dominated northern forests, separated from the subtropical habitats of southern Ganoderma species by climatic barriers, may have provided the ecological context for the emergence of G. tsugae as a conifer specialist. This connection between fungal macroevolution and major Earth history events is a genuinely compelling piece of deep natural history.

The Hemlock Adelgid Paradox

The hemlock woolly adelgid (Adelges tsugae)—an invasive scale insect causing widespread hemlock mortality across Appalachia and New England—is simultaneously G. tsugae’s greatest short-term benefactor and long-term existential threat. As dying hemlocks generate abundant fresh substrate, G. tsugae fruiting temporarily increases. But if eastern hemlock disappears from the landscape, the species’ primary North American substrate disappears with it. No other native North American tree currently serves as a confirmed substitute host for wild eastern populations.

Frequently Asked Questions About Ganoderma tsugae

Is Ganoderma tsugae the same as regular reishi?

No. “Regular reishi” typically refers to Ganoderma lucidum (European) or Ganoderma lingzhi (the species commercially cultivated in China and Japan for traditional medicine). G. tsugae is a distinct species, native to North America, with related but non-identical triterpenoid and polysaccharide profiles. While it is studied for many of the same biological activities, research results from G. lucidum human trials cannot be directly applied to G. tsugae. They are related cousins with overlapping, not identical, chemistry.

Can I grow Ganoderma tsugae at home?

Yes, with appropriate materials and patience. G. tsugae can be cultivated on sterilized supplemented hardwood or conifer sawdust blocks, or inoculated into pre-drilled logs. It is slower to colonize than oyster mushrooms or shiitake and is more vulnerable to Trichoderma (green mold) contamination. A liquid culture syringe is the most efficient inoculant, providing live, metabolically active mycelium for faster and more reliable colonization than spore-based methods.

What trees does Ganoderma tsugae grow on?

In eastern North America, almost exclusively on eastern hemlock (Tsuga canadensis) and occasionally Carolina hemlock (T. caroliniana). In Northeast China, where it is commercially cultivated, larch (Larix gmelinii) and firs (Abies spp.) serve as both wild and cultivated substrates. The extreme hemlock specificity in eastern North America is one of the species’ most ecologically unusual traits.

Does Ganoderma tsugae have human clinical evidence for its health claims?

No. As of March 2026, no randomized controlled trials or other controlled human studies have been published specifically for G. tsugae. Preclinical evidence (cell culture and rodent model studies) exists for antioxidant, hepatoprotective, cognitive protection, and anti-cancer activities, but these do not constitute human efficacy data. The research base is consistent with early-phase pharmaceutical research, not established clinical evidence.

How do I tell Ganoderma tsugae apart from other laccate Ganoderma?

The two most reliable macroscopic characters are substrate (hemlock only in eastern North America) and flesh color (pure white, not buff or tan). A KOH drop instantly turns the flesh black—useful but not species-specific for laccate Ganoderma broadly. In the western US, the conifer-associated laccate Ganoderma is likely G. oregonense, not G. tsugae; separating these two sister species reliably requires multilocus molecular analysis beyond ITS barcoding alone.

Where does Ganoderma tsugae originally come from?

North America. Despite being cultivated primarily in Taiwan and Northeast China today, G. tsugae was described in 1902 from specimens collected on eastern hemlock in the northeastern United States. It is a North American species that has been successfully adapted to cultivation in Asia. Popular sources describing it as “native to East Asia” or “originally from China” are incorrect.

Also available as a culture plate from Out-Grow.

Ganoderma tsugae Culture Plate