Xanthagaricus phylononcaeruleus Kun L. Yang, Jia Y. Lin, Zhen-Chao Liu & Zhu L. Yang
publication ID |
https://doi.org/ 10.11646/phytotaxa.659.2.2 |
DOI |
https://doi.org/10.5281/zenodo.13215555 |
persistent identifier |
https://treatment.plazi.org/id/9750879F-B129-FF8B-FAE7-19617D466937 |
treatment provided by |
Felipe |
scientific name |
Xanthagaricus phylononcaeruleus Kun L. Yang, Jia Y. Lin, Zhen-Chao Liu & Zhu L. Yang |
status |
sp. nov. |
Xanthagaricus phylononcaeruleus Kun L. Yang, Jia Y. Lin, Zhen-Chao Liu & Zhu L. Yang , sp. nov. ( Fig. 12 View FIGURE 12 )
Registration identifier:— FN571943
Etymology:— Structured from “ phylo -non - caeruleus ”, as this species is phylogenetically not recognized as X. caeruleus , but is morphologically very similar to X. caeruleus .
Diagnosis:— Similar to X. caeruleus , but differing from it by a shorter stipe (up to 24 mm) and narrower cheilocystidia (up to 10 μm wide).
Type:— China, Guangdong Province, Guangzhou City, Tianhe District, South China Agricultural University , a green belt in front of the College of Forestry and Landscape Architecture , on soil, 23°09’35”N, 113°21’39”E, elevation 30 m, April 23, 2023, Kun L.Yang & Jia Y. Lin, K 23155 ( HKAS133456 View Materials , GoogleMaps holotype! (ITS: PP736698; nrLSU: PP732928; rpb2: PP746785; tef-1α: PP746804 ); GoogleMaps HTBM0670 , isotype!) GoogleMaps .
Description:— Basidiomata small. Pileus 10–14 mm in diameter, hemispherical to plano-convex; background alabaster white (#F9F9F9) to overcast blue (#D6DBE7); squamules more or less flaky at center, becoming granular towards margin, dirty wisteria violet (#C5BCCC), steak purple (#877280), rosewood red (#78545C), blackcurrant purple (#422F45) to dull thatch red (#B29B9C), becoming lighter towards margin; margin with appendices concolorous with or lighter than the squamules on the pileus; context ceramic white (#FEFEFA) to merino white (#F9F5EC) when fresh, turning rust orange (#D79A65) or becoming darker after damaged. Lamellae free, subdistant to nearly crowded, alabaster white (#F9F9F9), dirty sky blue (#BED5DB) to sand green (#B2C4B5), with an entire to slightly serrate edge; lamellulae abundant. Stipe 16–24 mm long, 1.5–2 mm thick, cylindrical, slightly curved; background alabaster white (#F9F9F9) to lacewood brown (#D5B7A1); squamules fibrous to woolly, usually more abundant below the annulus, dirty wisteria violet (#C5BCCC) to desert orange (#E8D7B0); context ceramic white (#FEFEFA) to merino white (#F9F5EC) when fresh, turning rust orange (#D79A65) or becoming darker after damaged; base without tomenta. Annulus superior, easily broken and fugacious, concolorous with the squamules on the stipe. Odor fungal. Taste fungal.
Basidiospores [40/3/3] (5) 5.5–6 [5.81 ± 0.27, 6.00] × 3–3.5 [3.14 ± 0.22, 3.00] µm, Q = 1.57–2.00 [1.86 ± 0.15, 2.00], ellipsoid to oblong, slightly thick-walled, smooth under both LM and SEM, tinged ink green (#9DB1A7) to pale slate blue (#688D99) in both water and 5% KOH, with a small apiculus, with an indistinct germ pore. Basidia 8–15.5 × 5–7 μm, clavate to broadly clavate, 4-spored, thin-walled, nearly colorless in both water and 5% KOH, with sterigmata up to 2 µm long, surrounding by basidioles measured 7.5–14 × 3–7 μm. Lamella trama regular to subregular, composed of 3–11 µm wide, cylindrical to subcylindrical, thin-walled, nearly colorless in both water and 5% KOH, compact, moderately to frequently branching hyphae. Cheilocystidia very abundant, 18–26 × 7–10 µm, clavate, oblong to subcylindrical, thin-walled, smooth, nearly colorless in both water and 5% KOH. Pleurocystidia absent. Pileus squamules epithelioid, composed of globose, subglobose, ovoid to clavate, slightly thick-walled and encrusted cells measured 4.5–20 × 4.5–10 µm, tinged barley orange (#E4C8A4) in both water and 5% KOH. Stipe squamules intricate trichoid, composed of 3–10 µm wide, interwoven, flexuous, thin- to slightly thick-walled and encrusted, moderately to frequently branching hyphae, tinged pale brown (#E3DECC) in both water and 5% KOH. Clamp connections absent in all tissues.
Habitat and distribution:— Solitary to gregarious, seldom weakly caespitose, usually scattered on soil as individuals, in southern subtropical monsoon forests or urban green belts. Currently known from China (South China).
Additional collections examined:— China, Guangdong Province, Guangzhou City, Tianhe District, South China Agricultural University , a green belt in front of the College of Forestry and Landscape Architecture , on soil, 23°09’35”N, 113°21’39”E, elevation 30 m, June 30, Jia Y. Lin, L 23127 ( HTBM0960 (ITS: PP736710; nrLSU: PP732940 )) GoogleMaps ; same location, August 25, Jia Y. Lin, L 23318 ( HTBM1299 (ITS: PP736715; nrLSU: PP732945; rpb2: PP746802; tef-1α: PP746838 )) GoogleMaps ; same location, August 27, Jia Y. Lin, L 23323 ( HTBM1304 (ITS: PP736717; nrLSU: PP732947; rpb2: PP746786; tef-1α: PP746805 )) GoogleMaps ; same location, August 30, Jia Y. Lin , L23339 ( HTBM1320 (ITS: PP736720; nrLSU: PP732950 )), L23340 ( HTBM1321 (ITS: PP736721; nrLSU: PP732951 )) & L23346 ( HTBM1327 (ITS: PP736724; nrLSU: PP732954 )) GoogleMaps ; same location, August 31, Jia Y. Lin, L 23355 ( HTBM1336 (ITS: PP736725; nrLSU: PP732955 )) & L23356 ( HTBM1337 (ITS: PP736726; nrLSU: PP732956 )) GoogleMaps ; same location, September 4, Jia Y. Lin, L 23378 ( HTBM1359 (ITS: PP736731; nrLSU: PP732961 )) GoogleMaps ; same location, September 18, Jia Y. Lin, L 23444 ( HTBM1425 (ITS: PP736735; nrLSU: PP732965 )) GoogleMaps ; China, Guangdong Province, Guangzhou City, Huangpu District, Jiangdong Village , Boluoshan Hill , on soil, 23°11’31”N, 113°32’48”E, elevation 150 m, August 27, 2023, Zhen-Chao Liu, Kun L. Yang & Jia Y. Lin, S 23554 ( HTBM1665 (ITS: PP736745; nrLSU: PP732975 )) GoogleMaps ; same location, August 28, 2023, Zhen-Chao Liu, Kun L. Yang & Jia Y. Lin, S23569 ( HTBM1680 (ITS: PP736750; nrLSU: PP732980 )) GoogleMaps ; same location, August 31, 2023, Zhen-Chao Liu, Kun L. Yang & Jia Y. Lin, S23572 ( HTBM1683 (ITS: PP736751; nrLSU: PP732981 )) & S23573 ( HTBM1684 (ITS: PP736752; nrLSU: PP732982 )) GoogleMaps ; same location, September 6, 2023, Zhen-Chao Liu, Kun L. Yang & Jia Y. Lin, S23588 ( HTBM1699 (ITS: PP736753; nrLSU: PP732983 )), S23589 ( HTBM1700 (ITS: PP736754; nrLSU: PP732984 )), S23590 ( HTBM1701 (ITS: PP736755; nrLSU: PP732985 )) & S23591 ( HTBM1702 (ITS: PP736756; nrLSU: PP732986 )) GoogleMaps .
Additional notes: In the current phylogeny ( Fig. 2 View FIGURE 2 ), our collections mainly gathered from two different regions in Guangzhou, formed a stable clade with little internal variation and significant support (MLB=100%, BPP=1), presenting a distinct genetic distance from the clade formed by the holotype and paratype of X. caeruleus . Three species delimitation programs consistently supported these two groups to be two separate species, suggesting our collections represent a cryptic species of the X. caeruleus complex; thus, it’s named here as X. phylononcaeruleus . Stipe length and cheilocystidia width could be used to distinguish the two species.
It’s also notable that the stipe of X. phylononcaeruleus distinctly turns rust orange after damaged ( Fig. 12m View FIGURE 12 ). This reaction is not mentioned in the description in the protologue of X. caeruleus ( Hosen et al. 2018) , but as shown in the photo in the protologue (the Fig. 2A View FIGURE 2 in Hosen et al. 2018), X. caeruleus may also have this character. When mature, the stipe of X. phylononcaeruleus also presents an orangish to brownish tinge; it could be the result of a slow oxidation, essentially the same mechanism of the reaction after damage.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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