Research Article |
Corresponding author: Tolgor Bau ( junwusuo@126.com ) Academic editor: María P. Martín
© 2019 Qin Na, Tolgor Bau.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Na Q, Bau T (2019) Recognition of Mycena sect. Amparoina sect. nov. (Mycenaceae, Agaricales), including four new species and revision of the limits of sect. Sacchariferae. MycoKeys 52: 103-124. https://doi.org/10.3897/mycokeys.52.34647
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Phylogenetic reconstruction revealed that Mycena stirps Amparoina, which is traditionally classified in sect. Sacchariferae, should be treated at section level. Section Amparoina is characterised by the presence or absence of cherocytes, the presence of acanthocysts and spinulose caulocystidia. Eight species referred to Mycena sect. Amparoina sect. nov. are recognised in China. Of these taxa, four new species classified in the new section are formally described: M. bicystidiata sp. nov., M. griseotincta sp. nov., M. hygrophoroides sp. nov. and M. miscanthi sp. nov. The new species are characterised by the absence of both cherocytes and a basal disc, along with the presence of acanthocysts on the pileus, spinulose cheilocystidia and caulocystidia. Descriptions of the new species, accompanied by illustrations of morphological characters and comparisons with closely related taxa, are provided. A multi-locus analysis utilising the ITS + nLSU + SSU regions was carried out using maximum likelihood and Bayesian Inference. A key to the 12 species of sect. Amparoina sect. nov. and sect. Sacchariferae that are found in China is provided.
Agarics, new taxon, systematics, taxonomy
The genus Mycena (Pers.) Roussel is characterised by small basidiomata, thin and convex pileus with sulcate margin, non-deliquescent lamellae and hollow stipe (
Previous studies of sect. Sacchariferae have focused on species distributed in Europe and North and South America, with more than 60 species studied in the past 30 years (
A phylogenetic reconstruction of Mycena was incongruous with the traditional classification of stirps Amparoina within sect.Sacchariferae and indicated that the taxonomic classification of the section should be reconsidered. During our ongoing research on Mycena, four new taxa without a basal disc and cherocytes, belonging to the new section, were found in southern China in Chongqing City, Guangdong Province, Henan Province, Hubei Province, Tibet Autonomous Region, Yunnan Province and Zhejiang Province. These species are described here. Based on the phylogenetic analyses, an identification key to the 12 species of sect. Sacchariferae and sect. Amparoina currently known from China is provided.
Macroscopic characters were described from fresh specimens following conventional taxonomic methods. Colour terms and notations refer to those of
Material for DNA isolation was taken from dried specimens. Genomic DNA was extracted from samples using the NuClean Plant Genomic DNA Kit (Kangwei Century Biotechnology Company Limited, Beijing, China). The internal transcribed spacer (ITS) region was amplified with the primer pair ITS1 and ITS4 (
Taxa | Voucher | Locality | GenBank accession no. | ||
---|---|---|---|---|---|
ITS | nLSU | SSU | |||
Infundibulicybe gibba (Pers.) Harmaja | AFTOL-ID 1508 | USA | DQ490635 | DQ457682 | – |
I. gibba | FLAS-F-60947 | Unpublished | MH016906 | – | – |
Mycena abramsii (Murrill) Murrill | HMJAU 43282 | Jilin: Jingyuetan National Scenic Area, Changchun City | MH396626 | MK629348 | MK629326 |
M. abramsii | HMJAU 43468 | Jilin: Jingyuetan National Scenic Area, Changchun City | MH396627 | – | MK629328 |
HMJAU 43523 | Jilin: Songjiang Town, Jiaohe City | MH396628 | MK629350 | MK629330 | |
HMJAU 43606 | Inner Mongolia Autonomous Region: Mangui Town, Hulunbeier City | MH396629 | MK629355 | MK629336 | |
M. adscendens Maas Geest. | Orstadius329-05 | Norway: Strengsdal Village, Vestfold | KT900141 | – | – |
M. adscendens | Aronsen061119 | Norway: Strengsdal Village, Vestfold | KT900142 | – | – |
Aronsen120826 | Norway: Strengsdal Village, Vestfold | KT900143 | – | – | |
M. alphitophora | HMJAU 43498 | Jilin: Shenglihe forest farms, Jiaohe City | MH136830 | – | MK629329 |
HMJAU 43686 | Yunnan: Zixi Mountain National Nature Reserve, Chuxiong City | MH136831 | – | MK629343 | |
M. arcangeliana Bres. | 252b | Italy: Venice Museum of Natural History, Venice | JF908401 | – | – |
M. arcangeliana | 252f | Italy: Venice Museum of Natural History, Venice | JF908402 | – | – |
M. bicystidiata T.Bau & Q.Na | HMJAU 43589 | Hubei: Yandongwan, Lichuan County | MK309774 | – | – |
M. bicystidiata | HMJAU 43593 | Hubei: Xingdou Mountain National Nature Reserves | MK309775 | MK629354 | – |
HMJAU 43648, Type | Chongqing: Dafengbao Scenic Regions, Huangshui Town | MK309773 | MK629359 | MK629341 | |
HMJAU 43744 | Zhejiang: Tianmu Mountain National Nature Reserves, Hangzhou City | MK309776 | – | – | |
M. castaneicola T.Bau & Q.Na | HMJAU 43578, Type | Henan: Jigong Mountain National Nature, Xinyang City | MH136826 | – | MK629334 |
M. castaneicola | HMJAU 43581 | Henan: Bolden National Forest Park, Xinyang City | MH136827 | – | – |
M. citrinomarginata Gillet | HMJAU 43563 | Shanxi: Wutai Mountain National Nature, Xinzhou City | MG654739 | MK629351 | MK629331 |
M. citrinomarginata | 317h | Italy: Venice Museum of Natural History, Venice | JF908416 | – | – |
AD4TN | Tunisia: Aïn Draham | KU973883 | – | – | |
M. corynephora Maas Geest. | HMJAU 43574 | Henan: Xinyang City | MH136832 | – | MK629332 |
M. corynephora | HMJAU 43576 | Henan: Xinyang City | MH136833 | – | MK629333 |
M. diosma Krieglst.&Schwöbel | 320f | Italy: Venice Museum of Natural History, Venice | JF908417 | – | – |
M. griseotincta T.Bau & Q.Na | HMJAU 43800, Type | Yunnan: Shangri-La Pudacuo National Park | MK309783 | MK629363 | MK629346 |
M. griseotincta | HMJAU 43805 | Yunnan: Shangri-La Pudacuo National Park | MK309782 | – | – |
HMJAU 43819 | Tibet: Zhuqudeng Village, Nyingchi City | MK309784 | – | – | |
M. heteracantha (Singer) Desjardin | HMJAU 43709, | Hunan: Yuelu Mountain, Changsha City | MK309785 | MK629362 | MK629345 |
M. heteracantha | HMJAU 43711 | Hunan: Xiaoxi National Nature Reserves | MK309786 | – | – |
HMJAU 43716 | Hunan: Gaowangjie National Nature Reserves | MK309787 | – | – | |
M. hyalinostipitata T.Bau&Q. Na | HMJAU 43693, Type | Yunnan: Yeyahu Scenic Spot, Kunming City | MH136828 | MK629361 | MK629344 |
M. hyalinostipitata | HMJAU 43701 | Yunnan: Yeyahu Scenic Spot, Kunming City | MH136829 | – | – |
M. hygrophoroides | HMJAU 43417, Type | Guangdong: Chebaling National Nature Reserve, Shaoguan City | MK309780 | MK629349 | MK629327 |
HMJAU 43421 | Guangdong: Shangxie Village, Shaoguan City | MK309781 | – | – | |
M. meliigena (Berk.&Cooke) Sacc. | 39 | Italy: Venice Museum of Natural History, Venice | JF908423 | – | – |
M. meliigena | 39d | Italy: Venice Museum of Natural History, Venice | JF908429 | – | – |
M. miscanthi T.Bau & Q.Na | HMJAU 43573 | Henan: Jinniu Mountain, Xinyang City | MK309777 | MK629352 | – |
M. miscanthi | HMJAU 43582 | Henan: Bolden National Forest Park, Xinyang City | MK309778 | – | – |
HMJAU 43584, Type | Henan: Jigong Mountain National Nature, Xinyang City | MK309779 | MK629353 | MK629335 | |
M. pearsoniana Dennis ex Singer | FCME25817 | USA: Great Smoky Mountains National Park, Tennessee | JN182198 | – | – |
M. pearsoniana | TENN61544 | USA: Great Smoky Mountains National Park, Tennessee | JN182199 | – | – |
TENN61384 | USA: Great Smoky Mountains National Park, Tennessee | JN182200 | – | – | |
M. pelianthina (Fr.) Quél. | 108b | Italy: Venice Museum of Natural History, Venice | JF908379 | – | – |
M. pelianthina | 108f | Italy: Venice Museum of Natural History, Venice | JF908380 | – | – |
CBH164 | Denmark: Jutland, Paderup Mose | FN394548 | – | – | |
M. pseudocorticola Kühner | 124a | Italy: Venice Museum of Natural History, Venice | JF908386 | – | – |
M. pura (Pers.) P. Kumm. | HMJAU 43121 | Liaoning: Ant Ridge, Dandong City | MK309793 | – | – |
M. pura | HMJAU 43179 | Heilongjiang: Shengshan National Nature Reserve | MK309794 | – | – |
TENN65043 | USA: Great Smoky Mountains National Park, Tennessee | JN182202 | – | – | |
M. rosea Gramberg | CBH409 | Germany: Baden-Württemberg, Schwarzwald | FN394551 | – | – |
M. rosea | TL12409 | Denmark: Jutland, Skivum Nørrekrat | FN394557 | – | – |
M. rosella (Fr.) P. Kumm. | 938a | Italy: Venice Museum of Natural History, Venice | JF908488 | – | – |
M. rosella | Champ-21 | JGI MycoCosm database | KX449424 | – | – |
M. seminau A.L.C.Chew&Desjardin | ACL136 | Malaysia: Ulu Gombak, Selangor | KF537250 | – | – |
M. seminau | ACL308 | Malaysia: Ulu Gombak, Selangor | KF537252 | – | – |
M. silvae-nigrae Maas Geest.&Schwöbel | 515 | Italy: Venice Museum of Natural History, Venice | JF908452 | – | – |
M. silvae-nigrae | CC 13-12 | USA: Great Smoky Mountains National Park | KF359604 | – | – |
M. substylobates T.Bau & Q.Na | HMJAU 43418, Type | Guangdong: Chebaling National Nature Reserve, Shaoguan City | MH216189 | – | – |
M. substylobates | HMJAU 43444 | Guangxi Zhuang Autonomous Region: Nonggang National Nature Reserve, Chongzuo City | MH216190 | – | – |
M. supina (Fr.) P. Kumm. | 128a | Italy: Venice Museum of Natural History, Venice | JF908388 | – | – |
M. tenerrima Maas Geest. | HMJAU 43646 | Chongqing: Huangshui Town | MK309795 | – | MK629340 |
M. tenerrima | HMJAU 43816 | Tibet: Bomi County, Nyingchi City | MK309796 | MK629364 | – |
M. zephirus (Fr.) P. Kumm. | CBS 270.48 | Netherlands: Microbial Biological Resource Centres | MH856339 | – | – |
M. zephirus | CBS 273.48 | Netherlands: Microbial Biological Resource Centres | MH856341 | – | – |
A dataset, comprising sequences for the ITS + nLSU + SSU region from 96 accessions with taxonomic coverage of Europe, North America, Australia, Africa and Asia, was compiled and analysed. Sequences for 32 accessions were downloaded from GenBank and 64 newly generated sequences obtained in this study were aligned and adjusted manually using BioEdit 7.0.4.1 and Clustal X (
Sect. Amparoina (Clade 5) formed a distinct clade separated from sect. Sacchariferae (Clade 4), sect. Calodontes (Clade 3), sect. Supinaae (Clade 2) and sect. Fragilipedes (Clade 1), as a sister group to all other clades within the ingroup with high statistical support (ML ≥ 75%, BPP ≥ 1.00) and should be elevated to section level.
Phylogenetic reconstructions obtained using BI and ML showed similar topologies. The best-scoring Maximum Likelihood (ML) tree was selected as a representative phylogeny (Fig.
Samples of the four new species were placed in separate monophyletic lineages, each with high statistical support (M. bicystidiatum, ML = 99%, BPP = 1.00; M. griseotincta, ML = 99%, BPP = 1.00; M. hygrophoroides, ML = 98%, BPP = 0.99; M. miscanthi, ML = 100%, BPP = 1.00; Fig.
1 | Basal disc present, cherocytes absent, acanthocysts present, caulocystidia smooth or with few spines | (sect. Sacchariferae) 2 |
– | Basal disc present or absent, cherocytes present or absent, acanthocysts present, caulocystidia spinulose | (sect. Amparoina) 5 |
2 | Pileus grey-black | M. anoectochila |
– | Pileus white | 3 |
3 | Caulocystidia irregularly shaped | M. substylobates |
– | Caulocystidia fusiform | 4 |
4 | Cheilocystidia fusiform with spines in the middle part | M. tenerrima |
– | Cheilocystidia sphaeropedunculate with spines overall | M. hyalinostipitata |
5 | Basal disc and cherocytes present | (stirps Amparoina) 6 |
– | Basal disc and cherocytes absent | (stirps Alphitophora) 7 |
6 | Habitat on fruits of Castanea, pileus slightly pubescent | M. castaneicola |
– | Habitat on dead wood or humus layer, pileus with bran-like covering | M. heteracantha |
7 | Lamellae distant, L < 10, I < 3 | M. hygrophoroides |
– | Lamellae normal, L > 15, I > 6 | 8 |
8 | Basidiomata typically grey | M. griseotincta |
– | Basidiomata white | 9 |
9 | Caulocystidia of two types, sphaeropedunculate or clavate | M. bicystidiata |
– | Caulocystidia clavate | 10 |
10 | Basidiospores globose | M. corynephora |
– | Basidiospores ellipsoid | 11 |
11 | Acanthocysts of one type, sphaeropedunculate | M. miscanthi |
– | Acanthocysts of two types, globose or long-clavate | M. alphitophora |
Pileus densely pubescent to furfuraceous. Stipe arising from a well-developed basal disc or base swollen without a basal disc. Cheilocystidia with spines. Cherocystes present or absent. Acanthocysts present and overlying universal veil. Caulocystidia densely spinulose overall, never smooth.
Mycena spinosissima (Singer) Desjardin
Name refers to the name of stirps Amparoina.
Pileus furfuraceous to pruinose. Stipe without basal disc. Basidiospores small, 6.1–7.9 × 3.7–4.6 μm. Cheilocystidia clustered, sphaero-pedunculate to utriform with numerous sharp excrescences. Cherocytes absent. Acanthocysts pyriform to vesicular. Caulocystidia of two types, sphaero-pedunculate or clavate covered with conic spines. Clamps present.
CHINA. Chongqing City, Dafengbao Scenic Regions, 15 Aug 2017, Qin Na, HMJAU 43648.
Name refers to its two types of caulocystidia.
Pileus 2.8–5.2 mm in diam., conical when young, becoming nearly hemispherical with age, pure white all over, sulcate, translucent-striate, pruinose, furfur-like scattered, margin entire first, then nearly plane and finally fissile. Context very thin and fragile, pure white. Lamellae 0.5 mm thick, narrowly adnate, off-white, concolorous with the sides. Stipe slender, 15–28 × 0.5–1.0 mm, cylindrical, hollow, fragile, pure white, densely pruinose on the whole surface, base swollen and not forming a basal disc, hirsute. Odour and taste inconspicuous.
Basidiospores (5.6-)6.1–7.9(-8.3) × (3.5)3.7–4.6(4.9) μm, Q=1.6–2.0, ellipsoid to oblong-ellipsoid, hyaline, with drops, thin walled, amyloid. Basidia 20–26 × 6–9 μm, clavate, hyaline, 4- or 2-spored. Cheilocystidia 19–32 × 12–18 μm, clustered, sphaero-pedunculate to utriform with numerous sharp spines, thin-walled and hyaline, inamyloid. Pleurocystidia absent. Pileipellis hyphae 4–7 μm wide, weakly dextrinoid; cherocytes absent; a cutis overlaid by elements of universal veil, not in chains; acanthocysts of one type, numerous, pyriform to vesicular, 29–62 × 24–51 μm, inamyloid. Hyphae of the stipitipellis 3–14 μm wide, smooth, dextrinoid; caulocystidia abundant, of two types, utriform, sphaero-pedunculate, 21–85 × 14–66 μm or clavate, long-elliptic, 21–85 × 11–26 μm, densely and evenly spinulose overall, hyaline, thin-walled, inamyloid. Clamps present in all tissues.
Solitary to scattered on rotten wood in mixed forests, Bamboos, Cunninghamia, Ginkgo and Platycladus forests.
CHINA. Hubei Province, Enshi Tujia and Miao Autonomous Prefecture, Lichuan County, Yandongwan, 19 Jul 2017, Qin Na, HMJAU 43589; Xingdou Mountain National Nature Reserves, 20 Jul 2017, Qin Na, HMJAU 43593; Zhejiang Province, Hangzhou City, Tianmu Mountain National Nature Reserves, 4 Jul 2018, Qin Na and Tolgor Bau, HMJAU 43774.
Mycena bicystidiata is unique in sect. Amparoina stirps Alphitophora because of the two types of caulocystidia covered with conic spines. Mycena alphitophora, which is the most widely distributed species of sect. Amparoina, shows the most morphological similarities to M. bicystidiatum; however, the former differs in forming cylindric spores (7.5–10 × 4.5–5.5 μm), sphaero-pedunculate cheilocystidia and caulocystidia that are only clavate in shape (
Basidiomata of sect. Amparoina species. stirps Alphitophora: a–b Mycena alphitophora (Berk.) Sacc. c–d Mycena bicystidiata T.Bau & Q.Na e Mycena corynephora Maas Geest. f–g Mycena griseotincta T.Bau & Q.Na h Mycena hygroporoides T.Bau & Q.Na i Mycena miscanthi T.Bau & Q.Na; stirps Amparoina: j Mycena castaneicola T.Bau & Q.Na k–m Mycena heteracantha (Singer) Desjardin. Basidiomata of sect. Saccariferae species n–o Mycena hyalinostipitata T.Bau & Q.Na p–q Mycena substylobates T.Bau & Q.Na r Mycena tenerrima (Berk.) Quél. (=Mycena adscendens Maas Geest.) Scale bars: 10 mm (a–g, i–m, r), 5 mm (h, n–q). Photographs a–r by Qin Na.
Pileus, lamellae and stipe with greyish tint, especially when old. Stipe base swollen. Basidiospores pip-shaped. Pileipellis with two types of acanthocysts. Caulocystidia up to 200 μm long with spines.
CHINA. Yunnan Province, Diqing Tibetan Autonomous Prefecture, Shangri-La Pudacuo National Park, 14 August 2018, Qin Na, HMJAU 43800.
Name refers to the grey-tinted basidiomata.
Pileus 1.5–12.8 mm in diam., conical when young, campanulate with age, obtusely umbonate in the centre, translucent-striate, white, greyish-white when old (4B1), floccose, pubescent, pruinose, with crenate margin when young, then becoming nearly plane and finely torn. Context pure white, thin, fragile. Lamellae 0.2–0.5 mm thick, narrowly adnate or adnexed, pure white to slightly pale grey (4B1); edges finely torn, concolorous with the sides. Stipe 13–64 × 0.5–1.0 mm, central, terete, almost equal or slightly tapering to apex, hollow, greyish-white (5B1), pubescent or puberulous, with white, fine hairs, base swollen. Odourless, taste mild.
Basidiospores (5.6-)6.3–8.2(-8.5) × (3.5-)4.2–4.6(-5.2) μm, Q=1.5–1.9, Qav=1.7, pip-shaped, hyaline, guttulate, thin walled, amyloid. Basidia 19–23 × 7–9 μm, hyaline, clavate, 4-spored. Cheilocystidia 17–28 × 11–19 μm, oblong or clavate, with short and sharp spines, hyaline, inamyloid. Pleurocystidia absent. Pileipellis hyphae 6–10 μm wide, strongly dextrinoid; cherocytes absent; acanthocysts of two types, pyriform to vesicular, 8–22 × 7–18 μm or clavate to cylindric, 17–51 × 8–13 μm; universal veil composed of acanthocysts, globose, subglobose or sphaero-pedunculate, 28–67 × 26–58 μm, hyaline, covered with long, cylindrical excrescences or long and flexuous spinules, not in chains. Hyphae of the stipitipellis 2–7 μm wide, dextrinoid; caulocystidia abundant, clavate or long cylindrical, 77–216 × 9–11 μm, covered with densely conic spines, inamyloid. Clamps not seen.
Scattered to gregarious on litter layer in Quercus, Picea, Abies, Pinus mixed forests.
Yunnan Province, Diqing Tibetan Autonomous Prefecture, Shangri-La Pudacuo National Park, 15 August 2018, Qin Na, HMJAU 43805; Tibet Autonomous Region, Nyingchi City, Zhuqudeng Village, 20 August 2018, Qin Na, HMJAU 43819.
Mycena griseotincta is considered a new species in sect. Amparoina stirps Alphitophora on account of the absence of both a basal disc and cherocytes on the pileal surface (
Pileus concave with slight pruinose. Lamellae distant. Stipe with dense white fibrils and swollen base. Acanthocysts forming two types. Caulocystidia long-elliptic with conical excrescences, up to 120 μm long.
CHINA. Guangdong Province, Shaoguan City, Chebaling National Nature Reserve, 8 May 2017, Qin Na, HMJAU 43417.
Name refers to its sparse lamellae.
Pileus 1.5–2.5 mm in diam., campanulate to hemispherical, applanate or slightly concave at centre, white with greyish shade (6B1), shallowly sulcate, translucent-striate, slightly pruinose, pubescent. Context white, thin and very fragile. Lamellae distant, sparse, white, concolorous with the sides. Stipe 4.5–8.2 × 0.5–0.8 mm, cylindrical, hollow, fragile, pure white (5A1) with a greyish (5B1) base, covered with dense white fibrils, base swollen and not forming basal disc, hirsute. Odour and taste indistinctive.
Basidiospores (6.9-)7.2-8.9(-9.3) × (5.3-)6.4-6.7(-7.1) μm, Q=1.2–1.5, Qav=1.31, broadly-ellipsoid, hyaline in water and 5% KOH, amyloid, smooth. Basidia 15–21 × 7–9 μm, 4- or 2-spored, clavate, hyaline. Cheilocystidia 23–37 × 19–28 μm, subglobose, sphaero-pedunculate to utriform with numerous sharp spines, thin-walled and hyaline, inamyloid. Pleurocystidia absent. Pileipellis hyphae 3–9 μm wide, dextrinoid; cherocytes absent; a cutis overlaid by elements of universal veil, not in chains; acanthocysts forming two types, pyriform to vesicular, 13–29 × 11–24 μm, clavate to ovoid or obovoid, 29–42 × 14–20 μm, inamyloid. Hyphae of the stipitipellis 3–7 μm wide, smooth, dextrinoid; caulocystidia abundant, clavate, long-elliptic, 32–122 × 8–11 μm, with numbers of conical spines, inamyloid. Clamps present in all tissues.
Scattered on rotten wood of coniferous trees, ex. Cunninghamia.
Guangdong Province, Shaoguan City, Liangjiang Town, Shangxie Village, 7 May 2017, Qin Na, HMJAU 43421.
Mycena hygrophoroides could be considered to be a member of Hemimycena Singer owing to the tiny basidiomata and sparse lamellae, but the absence of a basal disc, amyloid spores and spinulose cheilocystidia, acanthocysts and caulocystidia are diagnostic characters for M. hygrophoroides, which should be placed in Mycena sect. Amparoina stirps Alphitophora. Mycena acanthophila J.C.Zamora&Català, of which the holotype was collected from Spain growing on dead branches of Leguminosae, most resembles M. hygrophoroides, but differs in having a yellow pileus, smaller cheilocystidia (13.5–22 × 8.5–12 μm) and diverse caulocystidia (Zamora and Català 2012). Mycena depilata, a species of stirps Alphitophora, shows some morphological similarities to M. hygrophoroides in possessing white and tiny basidiomata, distant lamellae (L = 7–9) and globose-pedicellate acanthocysts with hyaline contents. However, M. depilata differs in producing ellipsoid spores (Q = 1.64 ± 0.11), broadly clavate cheilocystidia and shorter caulocystidia (16–50 × 5–16 μm;
Growing on dead stem of Miscanthus. Pileus sparsely pruinose. Basidiospores cylindric. Cherocytes absent. Acanthocysts forming two types. Caulocystidia sphaero-pedunculate covered with spines. Clamps present.
CHINA. Henan Province: Xinyang City, Jigong Mountain, 16 Jul 2017, Qin Na and Tolgor Bau, HMJAU 43584.
Name refers to the substratum where the new species was found.
Pileus 3.5–7.8 mm in diam., hemispherical, broadly conical to convex, occasionally ± centrally depressed when young, sulcate, translucent-striate, pure white, pubescent to inconspicuously puberulous, margin nearly plane, undulate. Context white, thin, very fragile, about 1.0 mm thick at centre. Lamellae narrowly adnate or adnexed, off-white, concolorous with the sides. Stipe 26–38 × 0.5–1.0 mm, pure white, central, terete, hollow, equal, surface covered with slight white pubescent, base swollen but not discoid, pruinose. Odour and taste not distinctive.
Basidiospores (6.2-)6.7–8.6(-9.1) × (3.1)3.3–4.2(4.5) μm, Q=1.8–2.3, Qav=2.07, cylindric to narrow-ellipsoid, hyaline, guttulate, thin walled, amyloid. Basidia 18–24 × 6–9 μm, clavate, hyaline, 4-spored. Cheilocystidia 13–26 × 9–14 μm, abundant, lageniform, utriform or sphaero-pedunculate, with short and conical spines. Pleurocystidia absent. Pileipellis hyphae 3–8 μm wide, strongly dextrinoid; cherocytes absent; universal veil composed of acanthocysts, forming two types, pyriform, vesicular or clavate, 12–32 × 10–17 μm, inamyloid. Hyphae of the stipitipellis 2–8 μm wide, with coarse excrescences, 0.9–2.8 × 0.5–0.9 μm, strongly dextrinoid; caulocystidia abundant, elliptic, utriform, sphaero-pedunculate, 15–37 × 7–15 μm, with conical or cylindrical spines inamyloid. Clamps present in all tissues.
Solitary to scattered on dead stem of Miscanthus.
Henan Province, Xinyang City, Jinniu Mountain, 14 Jul 2017, HMJAU 43573; Xinyang City, Bolden National Forest Park, 17 July 2017, Qin Na and Tolgor Bau, HMJAU 43582.
The distinctive features of Mycena miscanthi include a white, granulose pileus, a pubescent stipe without forming a basal disc, narrow-ellipsoid spores, two types of acanthocysts and growth on dead stems of Miscanthus species. In combination, these features support the placement of M. miscanthi in sect. Amparoina stirps Alphitophora. Similar to M. miscanthi, M. alphitophora and M. depilata produce pure white basidiomata, cylindric spores and sphaero-pedunculate and spinulose cheilocystidia (
The present phylogenetic analysis showed that sect. Amparoina formed a distinct clade independent from sect. Sacchariferae with high BPP and BS support. This finding suggests that the presence of caulocystidia with dense spines is the most important character to separate sect. Amparoina from sect. Sacchariferae. However, in the presence of a basal disc, the species of sect. Sacchariferae are similar to stirps Amparoina and, in the acanthocysts on the pileus sect. Amparoina stirps, resembles sect. Amparoina Sacchariferae. It can be concluded that the difference in caulocystidia can be used to distinguish sect. Amparoina and sect. Sacchariferae and the basal disc and cherocytes are the basis of an infrasectional classification of sect. Amparoina. Thus, the circumscription of sect. Sacchariferae should be revised, for which the diagnostic characters are a well-developed basal disc, cherocytes absent, pileipellis a cutis not overlaid by elements of a universal veil composed of acanthocysts and caulocystidia smooth overall.
In morphology, sect. Amparoina and sect. Sacchariferae are closely allied with sect. Polyadelphiae Singer ex Maas Geest. and sect. Basipedes (Fr.) Quél (
Morphological characters and molecular evidence support the classification of the four new Mycena species as members of sect. Amparoina stirps Alphitophora. The four species share the same furfuraceous or farinose pileus, swollen stipe base without a basal disc, universal veil composed of acanthocysts and absence of both cherocytes and spinose caulocystidia. Mycena bicystidiatum is distinguished from M. griseotincta, M. hygrophoroides and M. miscanthi by producing two types of caulocystidia covered with conic spines. Mycena griseotincta is readily discriminated from M. bicystidiatum, M. hygrophoroides and M. miscanthi based on the greyish basidiomata and acanthocysts forming a universal veil with long, cylindrical excrescences. Compared with M. bicystidiatum, M. griseotincta, and M. miscanthi, M. hygrophoroides is distinct on account of the sparse lamellae and broadly ellipsoid basidiospores. Mycena miscanthi differ from M. bicystidiatum, M. griseotincta and M. hygrophoroides in growing on stems of Miscanthus and, in addition, the basidiospores are narrow ellipsoid.
It is worth mentioning that the placement of M. echinocephala (G.F. Atk.) Desjardin and M. cylindrospora A.H. Sm. remains unclear. The species are tentatively placed in stirps Alphitophora because of the lack of a basal disc on the stipe, but their caulocystidia are extraordinary in being smooth, terminated by a spinulose apex or smooth with an amorphous apex (
This study was supported by the National Natural Science Foundation of China (No. 31770010). We sincerely thank Prof Ping Zhang (Hunan Normal University, Changsha), Mrs Xiao-yan Wang (Hunan Normal University, Changsha), Mr Wen-fei Lin (Zhejiang University, Hangzhou), Mr Wei Zhou (Xinyang Agriculture and Forestry University, Xinyang), Mr Tsering Tamdrin (Nyingchi Municipal Science and Technology Bureau, Nyingchi), Drs Ming Zhang (Guangdong Institute of Microbiology, Guangzhou), Drs Feng-jian Wang (Hanjiang Normal University, Shiyan), Drs Zhu-xiang Liu (Jishou University, Jishou), Mr Zhong-yun Li (Shutterbug, Jishou), Mr Bing Xiao (Shutterbug, Jishou), Ya He (Hunan Normal University, Changsha), Jun Yan (Hunan Normal University, Changsha), Zong-ping Song (Guangdong Institute of Microbiology, Guangzhou), Xi-shen Liang (Guangdong Institute of Microbiology, Guangzhou), Li-qiang Wu (Jishou University, Jishou), Xue-qian Yi (Jishou University, Jishou) and Juan-juan Wang (Jishou University, Jishou) for their kind help during field work. We also thank Drs Yu-peng Ge (Ludong University, Yantai) and Drs Jun-qing Yan (Jiangxi Agricultural University, Nanchang) for their suggestions in writing this article.