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Scleroderma citrinum

Scleroderma citrinum, commonly known as the common earthball or pigskin poison puffball, is a gasteroid fungus in the family Sclerodermataceae, characterized by its tough, spherical to subspherical fruiting bodies measuring 2–12 cm in diameter, with a thick, warty rind that is yellowish to ochre-brown and often cracked or scaly. The internal gleba starts white or pale with a pinkish tinge in youth, maturing to a mottled purple-brown to black spore mass veined with white, releasing spores through irregular ruptures rather than a distinct pore; it lacks a true stipe but may attach to the substrate via rhizomorphs and emits a faint, unpleasant odor reminiscent of gas or rubber. This species is ectomycorrhizal, forming symbiotic relationships primarily with oak (Quercus) and other hardwood trees, and is widely distributed in temperate regions of Europe, North America, and beyond.^[1]^[2]^[3] Taxonomically, S. citrinum belongs to the phylum Basidiomycota, class Agaricomycetes, order Boletales, and genus Scleroderma, where it was first described by Christian Hendrik Persoon in 1801; it is closely related to boletes, particularly those in the genus Gyroporus, reflecting its evolutionary position among gasteromycetes. It thrives in acidic, sandy, or peaty soils in woodlands, heaths, and mossy areas, often along paths or in disturbed ground, fruiting from summer to late autumn (July to December in northern temperate zones). Ecologically, it enhances nutrient cycling in forest ecosystems through its mycorrhizal associations, which improve tree access to minerals like phosphorus, and it can influence soil bacterial communities by selecting for weathering bacteria; notably, it serves as a host for the rare parasitic bolete Pseudoboletus parasiticus, which grows on its fruiting bodies.^[3]^[4]^[5]^[1] Despite its superficial resemblance to edible puffballs or truffles, S. citrinum is poisonous and should not be consumed, as ingestion can cause severe gastrointestinal distress including nausea, vomiting, and diarrhea due to irritants like sclerocitrin; it is frequently misidentified by foragers, leading to accidental poisoning. While some reports suggest variability in toxicity, it is universally regarded as inedible in mycological literature, with its hard rind and internal coloration serving as key identifiers to distinguish it from safe species. Conservationally, it is common and not threatened, but its role in ectomycorrhizal networks underscores its importance in maintaining woodland biodiversity.^[3]^[2]^[6]

Taxonomy

Etymology and synonyms

The genus name Scleroderma derives from the Greek words sklēros (σκληρός), meaning "hard," and derma (δέρμα), meaning "skin," referring to the tough, leathery outer layer of the fruiting body.^[7] The specific epithet citrinum originates from the Latin citrinus, denoting "lemon-yellow," in reference to the characteristic coloration of the peridium.^[7]^[8] Scleroderma citrinum was first described scientifically by Christian Hendrik Persoon in 1801 in his Synopsis Methodica Fungorum.^[3]^[9] Historical synonyms include Scleroderma aurantium (Vaill. ex Pers.), based on Sébastien Vaillant's 1727 description as Lycoperdon aurantium and subsequently transferred by Persoon in 1801, and Scleroderma vulgare Hornem., published by Jens Wilken Hornemann in 1819.^[10] These names arose from 18th- and early 19th-century European mycological studies, with S. citrinum becoming the accepted basionym following nomenclatural revisions.^[10] Common names for S. citrinum vary regionally, reflecting its appearance and toxicity; in the United Kingdom, it is primarily known as the common earthball or citrine earthball, while in North America, it is called the pigskin poison puffball due to its textured, pigskin-like surface and poisonous nature.^[2]^[3] Other variations include golden earthball, emphasizing its yellowish hue.^[11]

Classification and phylogeny

Scleroderma citrinum is classified within the kingdom Fungi, phylum Basidiomycota, class Agaricomycetes, order Boletales, family Sclerodermataceae, and genus Scleroderma. This placement reflects its position among gasteroid basidiomycetes, which produce enclosed spore-bearing structures rather than open hymenia typical of many agarics and boletes.^[12] The species was first described by Christian Hendrik Persoon in 1801 in his Synopsis Methodica Fungorum, where it was established as the type species of the genus Scleroderma, initially encompassing a broad array of gasteroid fungi. Historical classifications of the genus underwent shifts as morphological and molecular data refined boundaries; early 19th-century treatments grouped Scleroderma with other puffball-like fungi, but by the late 20th century, it was firmly allied with Boletales based on spore and basidial characteristics.^[13] Recent phylogenetic analyses (2020–2025) utilizing internal transcribed spacer (ITS) and large subunit (LSU) ribosomal DNA sequences have affirmed S. citrinum as a distinct lineage within section Scleroderma of the genus, though earlier studies indicated non-monophyly suggestive of cryptic diversity.^[14]^[15] These investigations, primarily from Asian collections, reveal close relatives including undescribed or newly delimited taxa in southwestern China and northern Thailand, expanding the genus to over 20 recognized species globally.^[16] For instance, multi-locus phylogenies from Thai specimens positioned S. citrinum basal to clusters of novel species like S. separatum, highlighting regional endemism in Southeast Asia.^[17] In North America, including the southeastern United States, sequence data support S. citrinum as a widespread but potentially polyspecific complex, with subtle genetic variation warranting further resolution.^[14] A 2025 draft genome assembly of S. citrinum (strain hr), derived from specimens associated with chestnut trees (Castanea spp.), providing a genomic resource for the species, enabling future explorations of its ectomycorrhizal adaptations and phylogenetic affinities.^[18] This assembly, spanning approximately 40.4 Mb across 35 scaffolds, underscores S. citrinum's position relative to other Scleroderma species, such as the Asian S. yunnanense, in broader Basidiomycota phylogenies.^[19]

Description

Macroscopic characteristics

Scleroderma citrinum produces a fruiting body that is typically 2–10 cm in diameter and 2–6 cm in height, exhibiting a roughly spherical to slightly flattened or oval shape without a distinct stem. The peridium, or outer skin, is initially whitish to cream or pale yellow, developing into a yellowish to ochre-brown hue covered by irregular, wart-like scales that are coarse and well-separated; these scales darken to brownish or greenish tones with age, giving the surface a tough, leathery texture often compared to a warty potato. The fruiting body is attached to the substrate by thick white mycelial cords, and the rind measures 1–3 mm thick, sometimes cracking as it matures.^[1]^[3]^[2] Internally, the gleba begins as white and firm in young specimens, transitioning through a mottled purplish-gray stage to a mature dark olive-brown or purple-black mass of spores, which becomes powdery upon ripening; unlike true puffballs, it lacks a sterile stalk or a single apical dehiscence pore, instead rupturing irregularly at maturity to release spores through a ragged opening. The odor is generally unpleasant, often described as rubbery or gas-like, particularly in older fruiting bodies. For identification, a spore print yields a purple-black deposit.^[1]^[3]^[2]^[20] Development proceeds from a button-like young stage with a smooth, pale exterior and solid white interior to the mature form, where the peridium darkens and scales become prominent, and the gleba shifts colors while the overall structure persists as a durable, empty case for months after spore dispersal.^[1]^[3]^[2]

Microscopic characteristics

The microscopic characteristics of Scleroderma citrinum are essential for distinguishing it from other gasteroid fungi in the Sclerodermataceae, particularly through examination of the gleba and peridium under a light or scanning electron microscope. The basidiospores are globose to subglobose, measuring 7–12 µm in diameter (excluding ornamentation), with a thick wall up to 1.5 µm. They are dark purple-brown in mass but appear yellowish brown or dirty golden brown in 5% KOH, and are ornamented with short, densely packed spines or warts 1–1.5 µm long that frequently connect via low ridges to form a partially or fully reticulate pattern.^[1]^[21] The ornamentation varies even within a single specimen, ranging from merely spiny to strongly reticulate, providing a key diagnostic trait that separates S. citrinum from species with smoother or isolated-wart spores, such as some Lycoperdon taxa.^[1] The peridium is multilayered and up to 4 mm thick in fresh material, composed of clamped (fibulate) hyphae. It features an outer exoperidium of interwoven, thin-walled (ca. 1 µm) hyphae 4–12 µm wide that are hyaline to brownish yellow in KOH; a middle mesoperidium of septate, hyaline hyphae 2–8 µm wide with slightly thickened walls (ca. 2 µm); and an inner endoperidium of thin-walled, hyaline, clamped hyphae 2–4 µm wide.^[21]^[1] The hyphae throughout are smooth, with walls 1 µm thick and conspicuously clamped, contributing to the peridium's firm texture.^[1] Within the gleba, the capillitium comprises thick-walled, branched, septate hyphae forming an interwoven network among the developing spores, though this structure becomes inconspicuous or absent as the spore mass matures and darkens. Basidia are clavate, bearing four sterigmata, though they are often ephemeral and difficult to observe in mature specimens.^[21]

Distribution and habitat

Geographic range

Scleroderma citrinum is widely distributed worldwide, with confirmed occurrences in Europe, North America, parts of Asia, and Australia. In Europe, it is particularly common throughout the United Kingdom, where it appears frequently in various woodland and open habitats, as well as in Ireland and continental regions from Scandinavia to the Mediterranean.^[2]^[3] In North America, the species ranges from Canada—where it is documented in provinces such as Alberta, British Columbia, New Brunswick, Nova Scotia, Nunavut, Prince Edward Island, and Quebec—to the United States and southward into Mexico. Mexican records include collections from Jalisco and Veracruz, often in Pinus-Quercus forests and disturbed areas.^[4]^[22] In Asia, S. citrinum has been reported in China, particularly in southwestern regions like Yunnan, and in Thailand, where it is one of 11 documented Scleroderma species. It has been reported in northern Thailand, where recent studies from 2020 to 2025 have used morphological and molecular analyses to document various Scleroderma species, while Chinese fungal catalogues have expanded distribution data, noting occurrences in tropical and subtropical zones. These Asian records suggest possible introductions via international trade in ectomycorrhizal host trees, such as Eucalyptus. In Australia, it occurs in states like Queensland, often in eucalypt forests.^[23]^[24]^[17]^[25] The fruiting seasonality of S. citrinum varies by region but is primarily from late summer through autumn and winter in temperate zones, with peaks from July to November in the UK and similar patterns in North America. In warmer subtropical areas like parts of Mexico and Thailand, fruiting extends into summer months. Historical distributions align closely with current records, though expanded surveys in Asia indicate a potentially broader range than previously recognized, without clear evidence of climate-driven shifts.^[2]^[3]^[22]

Habitat preferences

Scleroderma citrinum thrives in acidic, well-drained soils, particularly those that are sandy, peaty, or mossy, and it favors disturbed or compacted ground such as forest paths, tracks, shaded banks, and the edges of drainage ditches.^[2]^[3] These conditions provide the nutrient-poor, humus-rich environments where the fungus commonly establishes, often avoiding alkaline or chalky soils that limit its growth.^[26] The fungus is frequently associated with mixed woodlands, heathlands, and grasslands, appearing under a variety of trees including oaks (Quercus spp.), pines (Pinus spp.), birches (Betula spp.), and chestnuts (Castanea spp.), as well as beeches (Fagus sylvatica) and spruces (Picea spp.).^[27]^[28] It occurs in these vegetated settings from summer through autumn, contributing to its prevalence in temperate forest understories.^[3] As a terrestrial species, S. citrinum grows directly on soil surfaces or in association with buried wood debris, typically emerging solitary or in small, scattered groups rather than dense clusters. This substrate preference aligns with its occurrence in drier microhabitats, where it demonstrates tolerance to drought stress and is noted during dry summer periods in suitable acidic soils.^[29]^[30]

Ecology

Symbiotic associations

Scleroderma citrinum is an ectomycorrhizal fungus that establishes mutualistic symbiotic associations with the fine roots of various woody plants, forming a protective hyphal mantle around root tips and a Hartig net that penetrates between root cells. This symbiosis enables the fungus to enhance the host's uptake of essential nutrients, particularly phosphorus and nitrogen, from the soil in exchange for photosynthetically derived carbohydrates supplied by the plant.^[14] Such associations are crucial for nutrient cycling in forest ecosystems, where the fungus acts as an early colonizer, rapidly spreading to young root systems in nutrient-poor environments like mining wastes.^[31] The fungus exhibits a broad host range with low specificity, forming ectomycorrhizae with trees in multiple families, including Pinaceae (such as pines), Betulaceae (birches), Fagaceae (oaks and chestnuts), and others like Fabaceae, Myrtaceae, and Salicaceae.^[14] A 2025 genomic study of S. citrinum strains isolated from Chinese chestnut (Castanea mollissima) trees underscores its role in establishing symbiosis with Fagaceae hosts, revealing genomic adaptations that support early-stage colonization and nutrient mobilization in these associations.^[31] These partnerships contribute to forest health by promoting host growth and resilience, with applications in reforestation projects for species like pines, poplars, and eucalypts.^[14] Beyond nutrient exchange, the ectomycorrhizal networks formed by S. citrinum improve soil structure by enhancing aggregation, which boosts aeration, and increase water retention capacity, aiding host plants in drought-prone habitats.^[32] Fruiting of S. citrinum is typically triggered by proximity to host roots and seasonal environmental cues, occurring from late summer through autumn in temperate regions.^[14] Additionally, these associations influence the diversity of soil bacterial communities in the mycorrhizosphere, potentially aiding mineral weathering and overall soil health.^[31]

Interactions with soil and other organisms

_Scleroderma citrinum influences the soil microbiome primarily through its mycorrhizosphere, where it selectively enriches bacterial communities associated with mineral weathering. In forest soils under oak (Quercus petraea) and beech (Fagus sylvatica), the mycorrhizosphere of S. citrinum shows a higher abundance of bacteria capable of efficient mineral dissolution, such as those in the genus Burkholderia, compared to bulk soil, thereby altering microbial community composition to favor weathering processes. This selective recruitment supports nutrient mobilization but does not broadly reduce overall bacterial diversity; instead, it promotes functional specialization in biogeochemical cycling. The fungus occasionally serves as a host to parasitic organisms, notably the bolete Pseudoboletus parasiticus, which emerges directly from the surface of S. citrinum fruiting bodies. This mycoparasitic interaction is specific, with P. parasiticus relying exclusively on earthballs like S. citrinum for nutrient acquisition, often observed in calcareous soils where both species co-occur.^[33] Such parasitism can compromise the host's reproductive structures, potentially limiting spore dispersal in affected populations.^[34] Regarding decomposition, S. citrinum exhibits limited saprotrophic activity, consistent with gene losses in ectomycorrhizal Boletales that impair organic matter breakdown capabilities. This results in minor contributions to the decomposition of buried wood or litter, with the fungus primarily facilitating nutrient cycling through indirect microbial interactions rather than direct enzymatic degradation. Extracts from S. citrinum demonstrate potential bioactivity against certain pathogens, including antiviral effects. A 2025 study on Thai specimens reported that methanol extracts inhibit Herpes simplex virus type 1 replication with an IC<sub>50</sub> of 15 µg/mL, highlighting possible ecological roles in suppressing viral propagation in soil-associated organisms, though chemical mechanisms remain under investigation.^[24]

Toxicity

Poisonous effects

Ingestion of Scleroderma citrinum primarily causes gastrointestinal distress, including nausea, vomiting, diarrhea, and abdominal cramps, with symptoms typically onsetting between 0.8 and 4 hours after consumption.^[35] These effects arise from irritant compounds in the fruiting body, leading to inflammation of the digestive tract.^[26] In severe cases, additional symptoms such as chills, sweating, and disorientation may occur, though recovery is usually complete with supportive care like fluid replacement and antiemetics.^[35] Inhalation of spores from mature S. citrinum fruiting bodies can trigger allergic reactions in sensitive individuals, manifesting as lacrimation, rhinitis, rhinorrhea, conjunctivitis, and dyspnea.^[27] More pronounced responses may include tachycardia and temporary unconsciousness, with onset as rapid as 0.1 to 1 hour.^[35] These respiratory and ocular irritations highlight the risks of handling or disturbing the fungus without precautions, particularly in enclosed spaces. While rarely fatal in humans, poisoning from S. citrinum necessitates prompt medical attention to manage dehydration and discomfort, as untreated cases can lead to significant morbidity.^[35] The fungus is frequently misidentified as edible puffballs (Lycoperdon spp.) or truffles due to its potato-like appearance, contributing to accidental ingestions.^[36] Such confusions contribute to mushroom poisoning incidents in North America. Case reports document multiple incidents in North America, including at least five adult human cases of gastrointestinal poisoning across states like Oregon and Pennsylvania, as compiled in the North American Mycological Association (NAMA) registry through 2005; more recent incidences may exist but are not comprehensively documented.^[35] In the United Kingdom, where S. citrinum is widespread, misidentification leads to frequent but underreported poisonings requiring hospitalization, often from foragers mistaking it for safe species.^[37] It has been reported as a cause of fungal intoxications in some European regions, such as Germany, underscoring the need for accurate identification.^[38]

Chemical compounds

Scleroderma citrinum contains several bioactive pigments that contribute to its coloration and toxicity, including the yellow pigment sclerocitrin and the orange-brown norbadione A, both derived from pulvinic acid. These compounds are primarily responsible for the fungus's characteristic hues in the peridium and gleba, with sclerocitrin providing the bright yellow tones and norbadione A contributing deeper shades. While norbadione A exhibits antioxidant and potential anticarcinogenic properties, sclerocitrin and related dimers have been isolated from the fruiting body and confirmed via nuclear magnetic resonance spectroscopy and X-ray crystallography.^[24] In addition to pigments, S. citrinum produces lanostane-type triterpenoids, such as (20S,22S,23E)-22-O-acetyl-25-hydroxylanosta-8,23(E)-dien-3-one, and steroids, which have been extracted from the fruiting body using methanol. Vulpinic acid derivatives, including 4,4'-dimethoxyvulpinic acid and its methyl ester, demonstrate antimicrobial activity, particularly against Mycobacterium tuberculosis, with minimum inhibitory concentrations in the range of 3.1–12.5 µg/mL for brominated and acetylated variants. These compounds also show cytotoxicity toward human cancer cell lines like NCI-H187, highlighting their bioactive potential despite overall toxicity. Melanin, another key compound, provides antioxidant, antibacterial, and light-barrier functions, isolated through alkaline extraction and purified via chromatography.^[39]^[40] Methanol extracts of S. citrinum have revealed antiviral activity against Herpes simplex virus type 1 with an IC<sub>50</sub> of 15 µg/mL, attributed to triterpenoid components. Starch isolated from the fungus exhibits physicochemical properties suitable for non-food applications, such as in cosmetics and adhesives, with amylose content of 38.5% and pasting temperatures of 70–75°C, suggesting utility in industrial formulations without bioactive risks. Extraction and detection of these compounds, including pigments and triterpenoids, are routinely achieved through high-performance liquid chromatography and mass spectrometry, targeting the gleba and peridium for optimal yield.^[24]^[41]

References

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Scleroderma citrinum (MushroomExpert.Com)
Jun 30, 2025 · A tough earthball with a yellowish to yellowish brown, prominently scaly outer surface. By maturity the scales are fairly large, well separated, and brownish.Missing: habitat | Show results with:habitat
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The fungus is very common and widespread throughout the UK. It prefers acid soils and mossy or peaty ground on heaths and in woodland, especially on sandy soil.Missing: taxonomy | Show results with:taxonomy
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### Summary of Synonyms for Scleroderma citrinum
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Apr 3, 2012 · ... cryptic diversity (Kirk et al., 2008) ... species Scleroderma citrinum and Scleroderma areolatum do not form monophyletic species groups.
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Phylogenetic analysis confirmed the placement of Scleroderma separatum based on the ITS and LSU regions (Fig. 1). S. separatum exhibits similar shapes and ...
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The genome sequences presented here will aid in further exploring the factors contributing to the establishment of ectomycorrhizal symbiosis in chestnut trees.
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Abstract Starches isolated from Scleroderma citrinum (SC) and Pleurotus ostreatus (PO) were investigated using physical and chemical tests.