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Article

Morphological Characteristics and Phylogeny Reveal Six New Species in Russula Subgenus Russula (Russulaceae, Russulales) from Yanshan Mountains, North China

by
Hao Zhou
1,
Gui-Qiang Cheng
1,
Qiu-Tong Wang
1,
Mei-Jun Guo
1,
Lan Zhuo
1,
Hui-Fang Yan
1,
Guo-Jie Li
2,3 and
Cheng-Lin Hou
1,*
1
College of Life Science, Capital Normal University, Xisanhuan Beilu 105, Beijing 100048, China
2
College of Horticulture, Hebei Agricultural University, Baoding 071001, China
3
Key Laboratory of Vegetable Germplasm Innovation and Utilization of Hebei, Collaborative Innovation Center of Vegetable Industry in Hebei, Baoding 071001, China
*
Author to whom correspondence should be addressed.
J. Fungi 2022, 8(12), 1283; https://doi.org/10.3390/jof8121283
Submission received: 11 November 2022 / Revised: 1 December 2022 / Accepted: 5 December 2022 / Published: 7 December 2022
(This article belongs to the Special Issue Edible and Medicinal Macrofungi)
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Abstract

:
Species of the genus Russula are key components of ectomycorrhizal ecosystems worldwide, some of which are famous edible fungi. Although many new species have been described in China, their diversity in North China is still poorly known. Based on the morphology observation of specimens and molecular phylogenetic analyses, combined with the current classification frame of Russula, six new species of Russula subgenus Russula are proposed from the Yanshan Mountains in northern Beijing and northern Hebei Province of China in this study: viz. Russula miyunensis (subsection Chamaeleontinae), R. plana (subsection Chamaeleontinae), R. sinoparva (subsection Puellarinae), R. sinorobusta (subsection Puellarinae), R. subversatilis (subsection Roseinae), and R. yanshanensis (subsection Puellarinae). This is the first report of the species of Russula subgenus Russula from the Yanshan Mountains. This study enriches the species diversity of Russula in North China and provides new data support for the systematic study of Russula in subsequent research, including research and development on edibility.

1. Introduction

Russula Pers. (Russulaceae, Russulales, Agaricomycetes, and Basidiomycota) was established in 1796, which is one of the most abundant genera, including at least 2000 species [1,2]. This genus is mainly characterized by colorless to multi-colored pileus, amyloid warty basidiospores, abundant spherocytes in a heteromerous trama, an absence of latex, and hyphae without clamp connections [3,4,5]. Russula is a large genus of ectomycorrhizal (ECM) fungi that are found in all common ecosystems, such as broad-leaved forest, coniferous forest, mixed coniferous, broad-leaved forest, or scrubland [6,7,8]. Furthermore, some members of Russula not only play an important role in ecology by symbiotic with a variety of plants but also serve as a food source for many animals, including humans. Some species of Russula, e.g., Russula delica Fr., Russula griseocarnosa X.H. Wang, Zhu L. Yang, & Knudsen, Russula nigricans Fr. et al., are famous edible fungi and important commercial trade goods in the world [7,9,10,11,12]. According to recent statistics on the diversity of Chinese edible macrofungi resources, there are about 70 edible species in China [12].
The previous classification system for Russula was based on morphology, e.g., pileus color, spore print, and spore. Miller and Buyck et al. first used phylogenetic analysis of nrITS loci to compare with the previous classification system of Russula in Europe, resulting in 78 Russula species forming six clades with higher supported values on the phylogenetic tree [13]. Buyck et al. [1,2] demonstrated that Russula was one of four monophyletic groups in non-corticoid Russulaceae and was divided into eight subgenera by multi-locus phylogenetic studies [1,14].
The subgenus Russula Pers. is a species-rich subgenus of Russula, which is morphologically characterized mainly by a great variation of basidiocarp size, pileus thick to extremely thin fleshed; stipe abnormally annulate gills unusually equal or lamellulae; spore print white to yellow; spores with amyloid suprahilar spot. Phylogenetically, this subgenus is divided into two parts: a core and a crown clade [1,2].
The first record of Russula in China is Russula alutacea (Fr.) Fr. from Tibet and Sichuan Province [15]. So far, about 190 species have been recorded in China [6,8,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31], and nearly 20 species belong to the subgenus Russula [18,23,26,32,33,34,35,36,37]. As a subgenus with the most species in the genus Russula, its members are also widely distributed all over the world.
The Yanshan Mountains (115°–119°47′ E, 39°40′–41°20′ N) are located in North China and have a warm temperate continental monsoon climate. This region is known for its high plant diversity. The main forest types of this region are deciduous broad-leaved forest and mixed coniferous and broad-leaved forest. Dominant ectomycorrhizal trees in this region include Pinus tabuliformis Carr, Betula spp., Quercus spp. and Abies (Mill.) spp. The Yanshan Mountains have an annual precipitation of approximately 350–700 mm, and their altitude ranges from 200 to 2200 m [37,38]. Until the present study, records about the Russula species in this area were very few [39].
In this study, six new species of the subgenus Russula crown clade from the Yanshan Mountains were described based on multi-locus phylogenetic analyses and detailed macro- and micromorphological data. The aims of this study are to identify the taxonomic status and phylogenetic position of new species, to establish a comprehensive database on the diversity of macrofungal in North China, especially the status of Russula in the Yanshan Mountains, and to use this as a basis for promoting research on macrofungal diversity and edible Russula species in this region.

2. Materials and Methods

2.1. Sampling and Morphological Observations

Specimens were collected from 2017 to 2021. Fresh specimens were photographed in the field, and characteristics such as color, odor, and viscosity were noted. Specimens were dried with a Dorrex dryer at 45 °C and deposited in the Herbarium of the College of Life Science, Capital Normal University, Beijing, China (BJTC). Macroscopic characteristics were recorded from fresh specimens. Microscopic characteristics were observed from thin sections of dried material mounted in 3% KOH or sterilized water. Congo Red (1%) was used to make the structures more visible. Melzer’s reagent was used to test the amyloid reaction of the spores [40]. All tissues were also examined in cresyl blue to verify the presence of ortho- or metachromatic reactions, as explained in Buyck [1]. Cystidia contents were examined in sulfovanillin (SV) solution [40]. Microscopic structures (e.g., basidiospores, basidia, cystidia) were observed and measured using a light microscope (Olympus DP71, Tokyo, Japan) and Image Pro Plus 6.0. The basidiospore structures were further observed under a field emission scanning electron microscope (SEM, Hitachi S-4800, Tokyo, Japan), digital cameras (Olympus U-TV0.5XC-3, Tokyo, Japan), and measuring software (Image Pro Plus 6.0). Basidiospore measurements were presented as (Min–) AV-SD–AV–AV + SD (–Max), where Min is the minimum value, Max is the maximum value, AV is the average value, SD is the standard deviation, and Q represents the length/width ratio of the basidiospores [8]. Statistics for the microscopic characteristics (e.g., basidiospores and basidia) were based on 30 measurements per specimen. The descriptive terms follow Adamčík et al. [2]. In this study, color codes were used from the reference website colorhexa (https://www.colorhexa.com (accessed on 8 September 2022)).

2.2. DNA Extraction and Sequencing

DNA extraction was achieved via the M5 Plant Genomic DNA Kit (Mei5 Biotechnology, Co., Ltd., Beijing, China). The DNA obtained was dissolved in 1 × TE buffer/sterile water and stored at −20 °C for later use. The PCR amplifications were performed in a Bio-Rad S1000TM Thermal Cycler (Bio-Rad Laboratories, Inc, Hercules, CA, USA). The primer set nrITS 1f/nrITS 4 was used to amplify for rDNA ITS region [41], T LR0R/LR5 for the large subunit nuclear ribosomal DNA (nuLSU rDNA) region [42], MS1/MS2 for the ribosomal mitochondrial small subunit (mtSSU) region [41], RBP2-6f/RBP2-7r for the second largest subunit of RNA polymerase II (rpb2) region [43] and tef1F/tef1R for the second largest subunit of transcription elongation factor 1-alpha (tef-1α) region [44], respectively. The PCR volume was 25 μL, and the detailed composition was described by Zhou et al. [39]. PCR amplification conditions for nrITS and nrLSU refer to Li et al. [25]. PCR amplification conditions for mtSSU and rpb2 refer to Song et al. [8]. PCR amplification conditions for tef-1α refer to Morehouse et al. [44]. DNA sequences were sequenced by Zhongkexilin Biotechnology, Co., Ltd., Beijing, China. Newly obtained sequences in this study were submitted to the NCBI GenBank database (https://submit.ncbi.nlm.nih.gov/ (accessed on 20 July 2022)). Accession numbers of sequences used for phylogenetic analyses are provided in Figure 1 and Table 1.

2.3. Molecular Phylogenetic Analyses

Raw reads of the generated DNA sequences were used to obtain consensus sequences using SeqMan v.7.1.0 (DNASTAR Inc., Madison, WI, USA). All sequences (nrITS, nrLSU, rpb2, tef-1α and mtSSU) were analyzed using MAFFT v.6 and manually trimmed using MEGA 6 [45]. All reference sequences of subgenus Russula of dataset were chosen for phylogenetic analyses based on previous studies and GenBank database in NCBI.
The nrLSU-rpb2-tef-1α-mtSSU multi-locus phylogenetic analysis included 83 ingroup samples, which were used to analyze the phylogenetic position of our specimens in the genus Russula. Moreover, the nrITS phylogenetic analysis included 129 ingroup samples, which were used to analyze the relationships among our collections and other species in the subgenus Russula. All reference sequences of subgenus Russula of the dataset were chosen for phylogenetic analyses based on previous studies and the GenBank database in NCBI and UNITE (accession number in Table 1 and Figure 2). Multifurca aurantiophylla (Bills & O.K. Mill.) Buyck and V. Hofst. (644/BB 09.119), Multifurca ochricompacta (Bills & O.K. Mill.) Buyck & V. Hofst. (BB02.107), M. ochricompacta (580/BB 07.010), Multifurca zonaria (Buyck & Desjardin) Buyck & V. Hofst. (DED7442), and Multifurca were outgroup taxa referring to Buyck et al. [1].
Jof 08 01283 g001 550
Figure 1. The nrITS phylogenetic tree obtained from the Bayesian analysis. Numbers above branches represent strongly and moderately support (pp ≥ 0.95 and/or MLB ≥ 50%). Numbers above branches are Bayesian posterior probability (pp) values and maximum likelihood bootstrap (MLB). The red font indicates the position of newly obtained sequences. Accession numbers of sequences information used are indicated on the figure. Asterisks (*) denote branches with pp = 1.00, MLb = 100%.
Figure 1. The nrITS phylogenetic tree obtained from the Bayesian analysis. Numbers above branches represent strongly and moderately support (pp ≥ 0.95 and/or MLB ≥ 50%). Numbers above branches are Bayesian posterior probability (pp) values and maximum likelihood bootstrap (MLB). The red font indicates the position of newly obtained sequences. Accession numbers of sequences information used are indicated on the figure. Asterisks (*) denote branches with pp = 1.00, MLb = 100%.
Jof 08 01283 g001
The maximum likelihood (ML) gene trees were estimated using the RAxML 7.4.2 Black Box software [38,46,47,48,49]. ML analysis used a GTR locus substitution model by running 1000 bootstrap replicates with all default settings parameters [50]. Bayesian inference (BI) phylogenetic analysis was performed using MrBayes v.3.1.2 [51]. Branch supports were calculated using a bootstrapping (BS) method with 1000 replicates [52]. Bayesian inference (BI) analysis was performed by the Markov chain Monte Carlo (MCMC) algorithm [53]. MrModeltest v. 2.3 was used to estimate the best model for Bayesian inference (GTR + I + G for nrITS, nrLSU, rpb2, and mtSSU; SYM + I + G for tef-1α) [51]. Two MCMC chains were run from the random trees for 10,000,000 generations and stopped when the mean standard deviation of split frequencies fell below 0.01. Trees were saved once every 1000 generations by the default settings. The first 25% of trees were discarded as the burn-in phase of each analysis. In the remaining trees, branches with significant Bayesian posterior probabilities were estimated, it has relatively stable topologies, and clades with high Bayesian posterior probability (pp) values can also illustrate relative relationships between species [54]. ML bootstrap support (BS) ≥ 50% and Bayesian posterior probability (PP) ≥ 0.95 were shown on the nodes in Figure 1 and Figure 2.

3. Results

3.1. Phylogenetic Analyses

The nrITS phylogenetic analysis included 129 ingroup samples, M. zonaria (DED7442) and M. ochricompacta (BB02.107) were used as the outgroups. The dataset of nrITS loci comprised 611 characters including alignment gaps. The best Bayesian tree is shown in Figure 1. The nrLSU-rpb2-tef-1α-mtSSU multi-locus phylogenetic analysis included 83 ingroup samples, M. ochricompacta (580/BB 07.010) and M. aurantiophylla (644/BB 09.119) were used as the outgroups. The dataset of multi-locus comprised 2511 characters including alignment gaps. The nrLSU-rpb2-tef-1α-mtSSU dataset was analyzed by ML analysis and BI analysis. Phylogenetic analysis generated topologies from ML analysis and BI analysis were almost identical, and the Bayesian tree are shown in Figure 2.
The nrLSU-rpb2-tef-1α-mtSSU and nrITS phylogenetic analyses revealed that the subgenera proposed by Buyck et al. [1] were well-supported with significant Bayesian posterior probability (PP) values and maximum likelihood bootstrap (MLB). Sequences of our collections all fell into the Russula subgenus Russula crown clade and formed six new lineages (marked in red and bolded in Figure 1 and Figure 2) with significant support. Thus, they were considered as six distinct clades and described as new species in this paper, i.e., Russula miyunensis, R. plana, R. sinoparva, R. sinorobusta, R. subversatilis, and R. yanshanensis.
The nrLSU-rpb2-tef-1α-mtSSU multi-locus phylogenetic analysis showed that two sequences of the new species Russula sinoparva (BJTC C540, BJTC Z441) were supported as one clade (pp = 1.00, MLB = 100%) and clustered with Russula odorata Romagn. Russula subversatilis (BJTC C653, BJTC T2001) formed one clade (pp = 0.99, MLB = 99%) together with Russula solaris Ferd. & Winge. Sequences of seven specimens of Russula yanshanensis (BJTC C561, BJTC Z421, BJTC Z1385, BJTC Z1305, BJTC L349, BJTC Z1448, and BJTC Z1390) were clustered together, forming a completely supported clade (pp = 1.00, MLB = 100%), R. yanshanensis clustered with Russula puellaris Fr. and formed a sister clade in the phylogenetic tree. Two new clades of Russula miyunensis (BJTC Z1355, BJTC Z1357) and Russula plana (BJTC Z1398, BJTC T2101) clustered with Russula olivascens Fr. formed a group (pp = 0.98, MLB = 99%). Sequences of three specimens of Russula sinorobusta (BJTC Z052, BJTC Z050, and BJTC Z662) clustered into a branch, with high support values (pp = 1.00, MLbs = 100%), and the branch further clustered a clade with Russula minutula Velen., Russula rosea Pers. and Russula sp. (735/BB 09.172) with moderate support.
The nrITS phylogenetic analysis showed similar topologies to that of multi-locus phylogenetic tree, and sequences of our collections also formed six strong support end branches. Notebly, R. subversatilis and R. sinoparva were clustered together with R. khinganensis G.J. Li & R.L. Zhao. Russula miyunensis and R. plana formed a well-supported clade. Russula sinorobusta formed a clade clustered with Russula lepidicolor Romagn. and Russula intermedia P. Karst. but without support values.

3.2. Taxonomy

Based on phylogenetic analyses and morphology, six new species of Russula subgenus Russula from the Yanshan Mountains were recognized and described in this study.
Russula miyunensis C. L. Hou, H. Zhou, & G. Q. Cheng, sp. nov.
Figure 3, Figure 4, Figure 5 and Figure 6.
MycoBank: MB 845047
Diagnosis:Russula miyunensis is diagnosed by small to big-sized basidiomata, light pink or grayish-yellow, central deep red to deep brown pileus, basidiospores ornamented with amyloid warts, and more or less chain-like, suprahilar spot obvious, longer basidia, shorter terminal cells near the pileus margin, pileocystidia without color change in sulfovanillin. Morphologically, R. miyunensis is similar to Russula olivascens Fr. and Russula clavatohyphata R.P. Bhatt, A. Ghosh, Buyck, & K. Das, but pileus of R. miyunensis has severely cracked when mature.
Holotype: CHINA, Beijing, Miyun District, Heilongtan, 40°33′42″ N, 116°46′20″ E, alt. 381 m, 29 August 2021, coll. C.-L.H., H.Z. and G.-Q.C. (BJTC Z1355).
Etymology: The epithet “miyunensis” referred to the locality “Miyun District” where the type specimen was collected.
Basidiomata: small to big size, pileus 32–135 mm in diameter, initially hemispherical when young, applanate with depressed in the center when mature, large pieces crack near the margin in age, smooth, peeling to 1/3 of the radius, margin light pink (#d69188) or grayish-yellow (#cec7a7), sometimes light yellow (#d59a6f), central deep red (#af4d43) to deep brown (#623f2d). Lamellae: white (#ffffff) to light yellow-brown (#ffffed), adnate, lamellulae absent, hardly forked. Stipe: 52–89 × 25–34 mm, white (#ffffff), sometimes with brownish (#a52a2a) on the base, cylindrical, inflated toward base, hollow, smooth. Context: 8–34 mm thick in half of the pileus radius, white (#ffffff), without color change when bruised. Spore print: not observed.
Basidiospores: (6.7–)6.9–7.4–7.9(–8.5) × (5.7–)6.1–6.4–6.7(–7) μm, [Q = (1.03–)1.09–1.17–1.23(–1.31)], globose to broadly ellipsoid, ornamentation of relatively small, dense [(5–)6–9(–10)] in a 3 μm diameter circle] amyloid warts, 0.3–0.7 μm high, occasionally with isolated warts, occasionally fused in pairs or triplets chains [0–2 in the circle], occasionally to frequently connected by short, fine line connections [1–3(–4) in the circle], suprahilar spot obvious, amyloid. Basidia: (35–)36.2–38.5–40.8(–43) × (10–)10.4–11.9–13.4(–15) μm, 2–4-spored, clavate, with particles and oil droplets, basidiola clavate or subcylindrical, ca. 7–12 μm wide. Hymenial cystidia: dispersed, ca. 400–600/mm2. Hymenial cystidia on lamellae sides: (45–)50.3–59.7–69.1(73–) × (10–)9.7–11–12.3(–13) μm, thin-walled, clavate, subfusiform or lanceolate, apically mainly obtuse, sometimes mucronate, often with 2–5 μm long appendage; contents with heteromorphous and granulose, turning light brown (#a52a2a) in SV. Hymenial cystidia on lamellae edges: smaller to hymenial cystidia on lamellae sides, (42–)44.4–50.2–56(–60) × (6.3–)7.4–8.5–9.6(–10) μm, clavate or subfusiform, apically often obtuse, sometimes with 2–3 μm long appendage, refracted inclusions, contents with heteromorphous-granulose, distribute mainly in the middle, relatively less, turning light brown (#a52a2a) in SV. Marginal cells: (15–)17.5–20.9–24.3(–27) × (3.0–)3.2–4.3–5.3(–6.4) μm, subcylindrical, occasionally flexible.
Pileipellis: orthochromatic in cresyl blue, sharply delimited from the underlying context, 35–60 μm deep, single-layered, weakly gelatinized, composed of relatively dense, intricate, horizontally oriented near the context, 2–7-μm-wide hyphae. Acid-resistant incrustations are present but mainly distinct only on subterminal cells of primordial hyphae, occasionally on terminal cells. Hyphal terminations near the pileus margin occasionally branched, sometimes flexuous, thin-walled; terminal cells (10.4–)12.9–18.7–24.5(–32.2) × (4.0–)4.8–5.7–6.6(–7.1) μm, mainly cylindrical, clavate, subfusiform or irregular shape, apically obtuse, occasionally attenuated, constricted or inflated, a few forked, subterminal cells often wider, ca. 2–8 μm wide, sometimes branched; hyphal terminations near the pileus center similar to those near the pileus margin; terminal cells (13–)15.8–19.7–23.6(–25) × (3.2–)3.7–4.8–5.9(–7.1) μm, cylindrical, clavate, subfusiform or irregular shape, apically obtuse, occasionally constricted or inflated, a few forked; subterminal cells often wider, sometimes branched, ca. 2–6 μm wide. Primordial hyphae near the pileus margin are always 2–3-celled, sometimes one-celled, thin-walled, terminal cells (20–)23.8–37.7–51.5(–71) × (4.0–)4.7–5.5–6.3(–7.2) μm, cylindrical or fusiform, apically usually obtuse, sometimes constricted; contents with heteromorphous-crystalline or banded, no color change in SV. Primordial hyphae near the pileus center are often smaller, always 2–3-celled, thin-walled, terminal cells (14–)23.2–33.1–43 (–48) × (3.4–)4.2–5.1–6(–8.1) μm, cylindrical or subfusiform, apically typically obtuse or occasionally attenuated, contents with heteromorphous-crystalline or banded. Cystidioid hyphae or oleiferous hyphae: not observed.
Habit and habitat: Scattered in broad-leaved forests of Carpinus turczaninowii Hance.
Additional specimens examined: CHINA, Beijing, Miyun District, Heilongtan, 40°33′42″ N, 116°46′20″ E, alt. 384 m, 29 August 2021, coll. C.-L.H., H.Z. and G.-Q.C. (BJTC Z1357).
Notes:Russula miyunensis belongs to subsection Chamaeleontinae Singer. On the phylogenetic tree, R. miyunensis is closely related to R. olivascens and R. plana (Figure 1). Morphologically, R. olivascens has light green-yellow pileus and bigger basidia (39–52 × 12–15 μm) than R. miyunensis; Russula plana has a small size, brick-red to deep red pileus, stipe with a pink tone, shorter basidia (23.4–33.2 × 12.1–15.9 μm), hymenial cystidia on lamellae sides turning light brown in SV. Moreover, the similarity of nrITS sequences with R. plana is 91.19% (coverage 99%) [55]. Russula miyunensis is similar to R. uttarakhandia A. Ghosh & K. Das, without molecular data, but R. uttarakhandia has a yellow to grayish-yellow color in the pileus middle, smaller basidia (28.5–37 × 12–15.6 μm), hymenial cystidia on lamellae edges without color change in SV, two-layered pileipellis, the absence of hymenial cystidia on lamellae edges, longer terminal cells of near the pileus margin (25–37 × 4–6 μm) [56].
Russula plana C. L. Hou, H. Zhou, & G. Q. Cheng, sp. nov.
Figure 7, Figure 8, Figure 9 and Figure 10.
MycoBank: MB 845049
Diagnosis:Russula plana is diagnosed by small-sized basidiomata, brick-red to deep red pileus, large basidiospores ornamented with amyloid warts or spines, suprahilar spot large, smaller basidia, longer terminal cells near the pileus margin, pileocystidia without color change in sulfovanillin. Russula plana and Russula clavatohyphata P. Bhatt, A. Ghosh, Buyck, and K. Das have similar morphological characteristics, but R. plana has brick-red to deep red pileus and small basidia and bigger basidiospores.
Holotype: CHINA, Beijing, Miyun District, Sileng Mountain, 40°28′22″ N, 117°6′17″ E, alt. 722 m, 30 August 2021, coll. C.-L.H., H.Z. and G.-Q.C. (BJTC Z1398).
Etymology: The epithet “plana” refers to the flat pileus of the basidiomata after maturity.
Basidiomata: small size, pileus 19–43 mm in diameter, initially hemispherical when young, applanate with depressed in the center when mature, recurved in age, smooth, sticky when wet, peeling to 1/5 of the radius. brick-red (#c62d42) to deep red (#622f30), sometimes red (#ff1a1a), margin light pink (#d69188). Lamellae: cream (#ffffff), yellow (#ffffed) in age, adnate to adnexed, lamellulae absent, hardly forked. Stipe: 23–41 × 6–13 mm, white (#ffffff), cylindrical, smooth, firm. Context: 5–10 mm thick in half of the pileus radius, white (#ffffff), without color change when bruised. Spore print: not observed.
Basidiospores: (6.8–)7.2–7.9–8.6(–9.9) × (5.8–)6.1–6.7–7.3(–8.3) μm, [Q = (1.02–)1.09–1.18–1.27(–1.44)], subglobose to broadly ellipsoid, ornamentation of relatively of small, dense [(5–)7–9(–10)] in a 3 μm diameter circle] amyloid warts or spines, 0.3–0.8 μm high, occasionally with isolated verrucous, occasionally to frequently fused in pairs or short chains [(0–)1–3(–4) in the circle], occasionally to frequently connected by short, fine line connections [(0–)1–3(–4) in the circle], suprahilar spot large, amyloid. Basidia: (22–)23.4–28.3–33.2(–38) × (10–)12.1–14–15.9(–18) μm, 2–4-spored, mainly clavate, sometimes broadly ellipsoid, with particles and oil droplets, basidiola broadly ellipsoid, clavate or subcylindrical, ca. 8–15 μm wide. Hymenial cystidia: dispersed, ca. 500–650/mm2. Hymenial cystidia on lamellae sides: (42–)48.2–57.1–66(–70) × (8.1–)9–10.4–11.8(–13) μm, clavate or subfusiform, apically mainly obtuse, often with 3–5 μm long appendage, thin-walled; contents with heteromorphous or granulose, turning grayish-red (#8b0000) in SV. Hymenial cystidia on lamellae edges: smaller to hymenial cystidia on lamellae sides, (36–)39.2–43.3–47.4(–50) × (6.5–)7.3–8.4–9.5(–10) μm, clavate or subfusiform, sometimes subulate, apically often obtuse or constricted, sometimes with 2–5 μm long appendage, refracted inclusions, contents with heteromorphous or granulose, turning ash black (#080808) in SV.
Marginal cells: (15–)20.2–25.5–30.8(–33) × (3.8–)3.1–4.8–5.7(–6.4) μm, subfusiform or irregular shape, sometimes flexible. Pileipellis: orthochromatic in cresyl blue, sharply delimited from the underlying context, 80–120 μm deep, single-layered, weakly gelatinized, relatively dense, intricate, horizontally oriented near the context, 4–9 μm wide hyphae. Acid-resistant incrustations present, distinct on the terminal or subterminal cells of primordial hyphae, occasionally on terminal cells. Hyphal terminations near the pileus margin occasionally branched, sometimes flexuous, thin-walled; terminal cells (13–)13.4–17.5–21.6(–26) × (3.8–)4.2–5.2–6.2(–7.8) μm, cylindrical, clavate, subfusiform or irregular shape, apically mainly obtuse, sometimes constricted or inflated, less forked, subterminal cells ca. 3–5 μm wide, occasionally branched; hyphal terminations near the pileus center similar to those near the pileus margin; terminal cells (8.4–)12–18–24(–35) × (3.0–)3.7–4.3–4.9 μm, cylindrical, clavate, subfusiform, subulate or irregular shape, apically obtuse, sometimes constricted or inflated; subterminal cells often wider, occasionally branched, ca. 3–6 μm wide. Primordial hyphae near the pileus margin are always single-celled, sometimes 2–3 celled, terminal cells (11–)14.9–21.4–27.9(–40) × (3.0–)3.7–4.3–4.9(–5.4) μm, thin-walled, mainly cylindrical, apically usually obtuse, sometimes attenuated; contents with less heteromorphous-granulose, no color change in SV. Primordial hyphae near the pileus center are often smaller, always single-celled, thin-walled, (15–)16.4–21.7–27(–32) × (3.0–)3.4–3.9–4.4(–5.2) μm, clavate, apically typically obtuse or occasionally attenuated, contents with heteromorphous-granulose. Cystidioid hyphae or oleiferous hyphae: not observed.
Habit and habitat: Individual or scattered in broad-leaved forests such as B. costata and P. davidiana trees.
Additional specimens examined: CHINA, Hebei Province, Chengde City, Xinglong County, Baboziling, 40°18′36″ N, 117°35′6″ E, alt. 880 m, 20 August 2021, coll. C.-L.H., R.-T.Z. and G.-Q.C. (BJTC T2101).
Notes:Russula plana belongs to subsection Chamaeleontinae. Phylogenetic analyses showed that R. plana, R. olivascens and R. miyunensis are closely related (Figure 1). Morphologically, R. miyunensis has light yellow to grayish-yellow, dark red and dark brown color in the pileus middle, colorless on the stipe, larger basidia (36.2–40.8 × 10.4–13.4 μm) than R. plana, hymenial cystidia on lamellae sides turning light brown in SV. Russula olivascens has light green-yellow pileus, bigger basidia (39–52 × 12–15 μm) than R. plana [57]. Russula plana is similar to R. clavatohyphata, which without molecular data, but R. clavatohyphata has short warty striate on the edge of the pileus, forked lamellae near the stipe, bigger basidia (22–54 × 9–13 μm) and smaller basidiospores (6.34–7.63 × 5.53–6.7 μm), hymenial cystidia on lamellae edges without color change in SV [30].
Russula sinoparva C. L. Hou, H. Zhou, & G. Q. Cheng, sp. nov.
Figure 11, Figure 12, Figure 13 and Figure 14.
MycoBank: MB 845048
Diagnosis:Russula sinoparva is diagnosed by small basidiomata, light pink to pink pileus, subglobose to broadly ellipsoid basidiospores ornamented with small amyloid warts, the absence of hymenial cystidia on lamellae edges, bigger hymenialcystida on lamellae sides. Russula sinoparva and Russula cessans A. Pearson have similar morphological characteristics, but R. sinoparva has light pink to pink pileus and smaller basidiospore, and bigger hymenial cystidia on lamellae sides.
Holotype: CHINA, Beijing, Huairou District, Erdaogou Village, 40°52′23.8″ N, 116°31′22.4″ E, alt. 758 m, 20 August 2019, coll. X.-Y.S., H.Z. and R.-T.Z. (BJTC Z441).
Etymology: The epithet “sinoparva“ refers to this Chinese species that has smaller basidiomata resembling the Russula parva Carteret & Reumaux.
Basidiomata: small size, pileus 18–30 mm in diameter, initially convex lenticular when young, flattened when mature, margin striations with small verrucas, sharp, cracked margin not obvious, light pink (#ffb6c1) to pink (#ffc0cb), central dark red (#ff0000) to strong deep red (#985144). Lamellae: white (#ffffff) to light yellow-brown (#ffffed), with 7–10 gills per cm at the edges, brittle, unequal, hardly forked. Stipe: 28–54 × 8–15 mm, white (#ffffff), sometimes brownish (#a52a2a), subcylindrical, smooth, firm, dilate gradually at the base. Context: 4–8 mm thick in half of the pileus radius, white (#ffffff) without color change when bruised. Spore print: not observed.
Basidiospores: (5.6–)6.5–7.0–7.6(–8.4) × (5.4–)5.8–6.3–6.7(–7.2) μm, [Q = (1.01–)1.04–1.13–1.21(–1.35)], subglobose to broadly ellipsoid, starchy ornamented, ornamentation of relatively small, moderately distant [(4–)5–7(–8) in a 3 μm diameter circle] amyloid warts, 0.3–1.0 μm high, occasionally to frequently fused in pairs or triplets, short-branched chains [(0–)1–3 (–4) in the circle], frequently connected by short or long, fine line connections [(0–)1–3 in the circle], suprahilar spot small. Basidia: (28–)29.6–34.5–39.4(–45) × (9–)10.5–11.8–13.1(–14) μm, 2–4-spored, clavate or fusiform, with particles and oil droplets, basidiola clavate or subcylindrical, ca. 5–15 μm wide. Hymenial cystidia: widely dispersed, ca. 200–300/mm2. Hymenial cystidia on lamellae sides: (30–)40.2–49.6–59.1(–67) × (7.2–)8.5–10–11.6(–13) μm, clavate or fusiform, apically often obtuse or mucronate, sometimes with 3–5-μm-long appendage, contents with refracted inclusions, or sometimes with granulose or crystalline, turning ash black (#0d0d0d) in SV. Hymenial cystidia on lamellae edges: not observed.
Pileipellis: orthochromatic in cresyl blue, sharply delimited from the underlying context, 70–100 μm deep, two-layered. Suprapellis 30–60 μm deep, strongly gelatinized, made up of ascending to erect, and slight interlaced hyphae. Subpellis 50–70 μm deep, composed of horizontally oriented, relatively dense, intricate, 3–6-μm-wide hyphae. Hyphal terminations near the pileus margin occasionally branched, sometimes flexuous, thin-walled; terminal cells (7.5–)14.7–23.5–32.4(–44) × (2.1–)2.6–3.4–4.1(–5.0) μm, mainly subcylindrical or clavate, apically mainly obtuse, occasionally attenuated, subterminal cells often wider, ca. 2–6 μm wide, always unbranched; hyphal terminations near the pileus center similar to those near the pileus margin; terminal cells (9–)16.7–31.9(–38) × (2.8–)3.1–4.3(–5.2) μm, mainly subcylindrical, occasionally ellipsoid, apically obtuse, constricted or attenuated; subterminal cells often wider, ca. 3–6 μm, always unbranched. Pileocystidia near the pileus margin are always 2–5-celled, a few one-celled, terminal cells (12–)18.1–32.6–47.2(–61) × (3.7–)4.7–5.9–7.2(–8.1) μm, thin-walled, mainly cylindrical or subcylindrical, occasionally clavate, apically usually obtuse, contents with granulose-heteromorphous, turning light ash black (#0d0d0d) in SV. Pileocystidia near the pileus center are often smaller, always 2–6-celled, thin-walled, terminal cells (12–)21.4–29.6–37.8(–45) × (4.8–)5.0–5.6–6.2(–7.2) μm, clavate or cylindrical, apically typically obtuse or occasionally attenuated, contents with granulose or occasionally crystalline. Cystidioid hyphae: in subpellis and context with heteromorphous-granulose contents, oleiferous hyphae in the subpellis close to the context.
Habit and habitat: Individual or scattered in coniferous forests and mixed coniferous and broad-leaved forests of Pinus tabuliformis Carr. and Juglans mandshurica Maxim.
Additional specimens examined: CHINA, Beijing, Huairou District, Sunzhazi Village, 40°56′39.1″ N, 116°30′23.4″ E, alt. 780 m, 25 August 2020, coll. C.-L.H., R.-T.Z. and G.-Q.C. (BJTC C540).
Notes:Russula sinoparva belongs to the subsection Puellarinae Singer. Phylogenetic analyses revealed that R. sinoparva is related to R. odorata, R. khinganensis, and R. subversatilis (new species in this paper) (Figure 1 and Figure 2). Morphologically, they are somewhat similar in pileus shape and basidia size. However, R. sinoparva is diagnosed by the light pink to pink, central dark red to deep red pileus, strongly gelatinized suprapellis, 1–3-celled pileocystidia near the pileus margin; R. odorata is distinguished from R. sinoparva by the central brown or olive pileus and irregularly bifurcated lamellae. R. khinganensis by the livid brown or deep livid brown to russet vinaceous pileus and thicker pileipellis [24], and R. subversatilis by the light gray-red to deep red, central yellowish-brown to dark red pileus, bigger basidia and hymenial cystidia on lamellae sides. Russula cessans, which is without molecular data, is similar to R. sinoparva in lamellae color and density, but it has a pileus of black color in the middle and smooth, unstriped edges, bigger spores (8–9 × 7–8 µm) and smaller hymenial cystidia on lamellae sides (7–9 µm) [58].
Russula sinorobusta C. L. Hou, H. Zhou, & G. Q. Cheng, sp. nov.
Figure 15, Figure 16, Figure 17 and Figure 18.
MycoBank: MB 845050
Diagnosis:Russula sinorobusta is diagnosed by small to medium-sized basidiomata, gray-red to rose red, central deep red pileus, basidiospores ornamented with small amyloid warts, suprahilar spot small, longer basidia, shorter hymenial cystidia on lamellae sides, pileocystidia absent. Morphologically, R. sinorobusta is similar to R. intermedia and Russula vinosa Lindblad., but R. sinorobusta has gray-red to rose red, central deep red pileus, and smaller basidiospore.
Holotype: CHINA, Beijing, Changping District, Yanshou Temple, 40°22′23.3″ N, 116°19′22.3″ E, alt. 270 m, 14 August 2019, coll. J.-Q.L. and H.Z. (BJTC Z052).
Etymology: The epithet “sinorobusta” refers to the stipe of this Chinese species that is relatively sturdy, resembling the Russula robusta R. Heim.
Basidiomata: small to medium size, pileus 51–82 mm in diameter, initially hemispherical when young, applanate with depressed in the center when mature, sometimes convex, slightly curved in edges, smooth when young, wrinkle in age, sticky when wet, peeling to 1/5 of the radius. gray-red (#8e6f70) to rose red (#b57281), sometimes deep red (#3b1f1f) in the center. Lamellae: white (#ffffff) to light yellow-brown (#ffffed), with 9–11 gills per cm at the edges, adnate, equal, lamellulae absent, hardly forked. Stipe: 60–102 × 19–34 mm, white (#ffffff), cylindrical, becoming hollow when mature, slightly inflated near the base, longitudinally striate. Context: 13–21 mm thick in half of the pileus radius, white (#ffffff), without color change when bruised. Spore print: not observed.
Basidiospores: (5.7–)6.2–6.6–7(–7.4) × (5.3–)5.5–5.9–6.3(–7.3) μm, [Q = (1.01–)1.06–1.12–1.18(–1.22)], subglobose to broadly ellipsoid, ornamentation of relatively of small, moderately distant to dense [(4–)5–8(–10)] in a 3 μm diameter circle] amyloid warts, 0.2–0.7 μm high, with abundant isolated verrucous, occasionally fused in pairs, triplets or short chains [0–2(–3) in the circle], occasionally connected by short, fine line connections [0–2(–3) in the circle], suprahilar spot small, weakly amyloid. Basidia: (35–)41.1–46–50.9(–57) × (11–)11.4–12.5–13.6(–14) μm, 2–4-spored, clavate or broadly ellipsoid, with particles and oil droplets, basidiola clavate or subcylindrical, ca. 6–10 μm wide. Hymenial cystidia: moderately numerous, ca. 720–900/mm2. Hymenial cystidia on lamellae sides: (60–)70.9–80.3–89.7(–94) × (10–)10.4–11.1–11.8(–12) μm, thin-walled, clavate or fusiform, apically mainly obtuse, occasionally mucronate or constricted, with 3–7-μm-long appendage; contents with granulose or banded, turning gray (#808080) to grayish purple in SV. Hymenial cystidia on lamellae edges: smaller and narrower to hymenial cystidia on lamellae sides, (40–)43.1–50–56.9(–63) × (6.0–)6.4–7.5–8.6(–10) μm, clavate or subcylindrical, apically often obtuse, sometimes with 2–4 μm long appendage, contents with granulose or banded.
Marginal cells: (14–)14.9–20.6–26.3(–33) × 5.8–6.5–7.2(–8.1) μm, cylindrical orclavate. Pileipellis: orthochromatic in cresyl blue, sharply delimited from the underlying context, 100–190 μm deep, two-layered. Suprapellis 50–100 μm deep, weakly gelatinized, composed of ascending to erect hyphae, trichoderm. Subpellis 45–90 μm deep, strongly gelatinized, composed of horizontally oriented, relatively dense, intricate, 3–9-μm wide hyphae. Hyphal terminations near the pileus margin occasionally branched, sometimes flexuous, thin-walled; terminal cells (14–)14.3–57.6(–62) × 2–4 μm, mainly cylindrical or subcylindrical, apically obtuse, subterminal cells often wider, ca. 2–3 μm wide, always unbranched; Hyphal terminations near the pileus center similar to those near the pileus margin; terminal cells (15–)15.6–45.3(–47.8) × (2–)3–5 μm, cylindrical, apically obtuse; subterminal cells often wider, always unbranched, ca. 2–3 μm wide. Pileocystidia not observed. Cystidioid hyphae or oleiferous hyphae: not observed.
Habit and habitat: Individual or scattered in broad-leaved forests of Castanea mollissima Blume.
Additional specimens examined: CHINA, Beijing, Changping District, Yanshou Temple, 40°22′23.3″ N, 116°19′22.5″ E, alt. 270 m, 14 August 2019, coll. J.-Q.L. and H.Z. (BJTC Z050); CHINA, Beijing, Changping District, Yanshou Temple, 40°22′7.4″ N, 116°19′21.7″ E, alt. 223 m, 26 July 2019, coll. G.-Q.C. and H.Z. (BJTC Z662).
Notes:Russula sinorobusta belongs to subsection Roseinae Singer ex Sarnari. Multi-loci phylogenetic analysis showed that R. sinorobusta, R. minutula and R. rosea are closely related (Figure 1). Russula sinorobusta may be related to Russula lepidicolor Romagn. and Russula intermedia P. Karst., but not have supported value in ITS tree (Figure 2). Morphologically, R. sinorobusta is similar to R. intermedia and R. vinosa, but R. vinosa has a short and fuzzy striate on the edge of the pileus, the pileus middle color is copper, ochre, or brown, and the lamellae is close to the stipe forked, stipe hollow, larger basidiospores (8–11.5 × 6.5–8.5 μm) and hymenial cystidia on lamellae sides (85–120 × 10–13 μm) than R. sinorobusta [55]. Russula intermedia has wider hymenial cystidia on lamellae edges (9–11 μm) than R. sinorobusta, the width of pileocystidia is 4–11 μm, and with lilac color in SV [39].
Russula subversatilis C. L. Hou, H. Zhou, & G. Q. Cheng, sp. nov.
Figure 19, Figure 20, Figure 21 and Figure 22.
MycoBank: MB 845051
Diagnosis:Russula subversatilis is diagnosed by light gray-red to deep red, central yellowish-brown to dark red pileus, basidiospores ornamented with amyloid warts or spines, and more or less reticulate or chain-like, bigger basidia and hymenial cystidia on lamellae sides, light red pileocystidia in sulfovanillin. Russula subversatilis and R. versatilis Romagn have similar morphological characteristics, but R. subversatilis has light gray-red to deep red, central yellowish-brown to dark red pileus, shorter basidiospore, and narrower pileocystidia.
Holotype: CHINA, Beijing, Miyun District, Heilongtan, 40°33′38.1″ N, 116°46′55.8″ E, alt. 255 m, 27 August 2020, coll. C.-L.H. and G.-Q.C. (BJTC C653).
Etymology: The epithet “subversatilis” refers to its morphological similarity to Russula versatilis Romagn.
Basidiomata: small to medium size, pileus 32–55 mm in diameter, initially hemispherical when young, flattened when mature, slightly concave in the middle, slightly curved in the margin, sticky when wet, with inconspicuous striations, margin light gray-red (#b09a95) to deep red (#985144), central yellowish-brown (#aa8d6f) to dark red (#481c1c). Lamellae: white (#ffffff) to light yellow-brown (#ffffed), with 5–7 gills per cm at the edges, free, brittle, lamellulae absent, hardly forked. Stipe: 35–65 × 15–20 mm, white (#ffffff), sometimes with brownish (#a52a2a) on the base, cylindrical, smooth, firm. Context: 8–14 mm thick in half of the pileus radius, white (#ffffff), without color change when bruised. Spore print: not observed.
Basidiospores: (6.1–)6.6–7.1–7.6(–8.2) × (5.3–)5.7–6.1–6.6(–7.3) μm, [Q = (1.02–)1.09–1.17–1.25(–1.32)], subglobose to broadly ellipsoid, ornamentation of relatively small, moderately distant to dense [(5–)6–9(–10) in a 3 μm diameter circle] amyloid warts or spines, 0.4–0.9 μm high, occasionally formed reticulate, occasionally to frequently fused in short or long branched chains [(0–)1–3 (–5) in the circle], occasionally connected by short or long, fine line connections [(0–)1–2(–3) in the circle], suprahilar spot small, amyloid. Basidia: 33.5–37–40.5(–45.2) × (11.8–)12.6–13.6–14.5(–15.2) μm, 2–4-spored, clavate, with particles and oil droplets, basidiola clavate or subcylindrical, ca. 9–14 μm wide. Hymenial cystidia: moderately numerous, ca. 950/mm2. Hymenial cystidia on lamellae sides: (47.6–)53.2–58.7–64.2 (–65.3) × (9.2–)10.5–11.9–13.3(–14.1) μm, clavate or subfusiform, apically mainly obtuse, often with 5–7-μm-long appendage, thin-walled; contents with heteromorphous-crystalline or granulose, mainly in the middle and upper part, turning purple (#800080) in SV. Hymenial cystidia on lamellae edges: similar to hymenial cystidia on lamellae sides, (36.5–)42.7–49.5–56.3(–64.4) × (6.9–)7.4–8.5–9.6(–10.1) μm, clavate or subfusiform, apically often obtuse, sometimes with 2–6-μm-long appendage, contents with granulose or crystalline, turning purple (#800080) in SV.
Marginal cells: (14.2–)15.6–17.8–20(–21.5) × (7.8–)8.4–9.2–10.1(–11.4) μm, usually broadly clavate and shorter than basidiola. Pileipellis: orthochromatic in cresyl blue, sharply delimited from the underlying context, 90–140 μm deep, two-layered. Suprapellis 40–60 μm deep, less gelatinized, composed of relatively loose, ascending to erect hyphae. Subpellis 60–100 μm deep, strongly gelatinized, composed of relatively dense, intricate, horizontally oriented near context, 2–7 μm wide hyphae. Hyphal terminations near the pileus margin occasionally branched, sometimes flexuous, thin-walled; terminal cells (12.4–)16.1–21.9–27.7(–32.4) × (2.0–)2.5–3.3–4.1(–5.1) μm, mainly cylindrical, sometimes clavate or fusiform, apically obtuse or constricted, subterminal cells often wider, ca. 2–4 μm wide, occasionally branched; hyphal terminations near the pileus center similar to those near the pileus margin; terminal cells (10.2–)12.9–23.5(–28.7) × (2.0–)2.3–4.1(–4.9) μm, cylindrical or subfusiform, apically obtuse, sometimes attenuated or constricted; subterminal cells often wider, occasionally branched, ca. 2–5 μm wide. Pileocystidia near the pileus margin are always 2–3 celled, sometimes one-celled, thin-walled, terminal cells (30.2–)35–67.8(–88.4) × (3.0–)3.5–5.3(–6.1) μm, cylindrical, subclavate or subfusiform, apically usually obtuse, sometimes attenuated, contents with abundant, heteromorphous, granulose or occasionally crystalline, turning light ash black (#0d0d0d) to light red (#ff4d4d) in SV. Pileocystidia near the pileus center are often smaller, always 2–3-celled, thin-walled, (21.4–)25.5–60.7(–78.1) × (3.8–)4.1–5.7(–6.0) μm, cylindrical or subclavate, apically obtuse, contents with heteromorphous, granulose. Cystidioid and oleiferous hyphae: not observed.
Habit and habitat: Individual in broad-leaved forests of Carpinus turczaninowii.
Additional specimens examined: CHINA, Beijing, Miyun District, Heilongtan, 40°33′38.2″ N, 116°46′56.2″ E, alt. 265 m, 27 August 2020, coll. C.-L.H. and G.-Q.C. (BJTC T2001).
Notes:Russula subversatilis belongs to the subsection Puellarinae. The phylogenetic trees (Figure 1 and Figure 2) show that R. subversatilis is closely related to Russula carpini R. Girard & Heinem, Russula khinganensis G.J. Li & R.L. Zhao, and Russula solaris Ferd. & Winge, but R. carpini has light brownish purple or yellow pileus, bigger basidiospores (7–10 × 6.5–8 μm) [57], R. khinganensis has thinner basidia (35–43 × 10–11 μm), and hymenial cystidia on lamellae sides (51–65 × 6–9 μm), no hymenial cystidia on lamellae edges [24], R. solaris has pale orange to tinged yellowish pileus, bigger basidia (40–52 × 12–14 μm) and basidiospores (7.5–9 × 6.5–7.5 μm) [59]. Morphologically, R. versatilis, which is without molecular data, is similar to R. subversatilis in light gray-red pileus, light yellow-brown lamellae, and basidiospores with isolated warts or spines. However, R. versatilis has a pink or cream color in the middle pileus, longer basidiospores (7–8.5 × 5–6 µm), and wider pileocystidia (6–8 µm) [60].
Russula yanshanensis C. L. Hou, H. Zhou, & G. Q. Cheng, sp. nov.
Figure 23, Figure 24, Figure 25 and Figure 26.
MycoBank: MB 845052
Diagnosis:Russula yanshanensis diagnosed by light pink to pink, central light yellow to yellowish-brown pileus, smaller basidiospores ornamented with amyloid warts, and frequently chain-like, shorter hymenial cystidia on lamellae sides and hymenial cystidia on lamellae edges. Russula yanshanensis and Russula cremeirosea Murrill have similar morphological characteristics, but R. yanshanensis has pink, central light yellow to yellowish-brown pileus, shorter basidiospore, shorter hymenial cystidia on lamellae sides and hymenial cystidia on lamellae edges.
Holotype: CHINA, Beijing, Huairou District, Sunzhazi Village, 40°56′35″ N, 116°30′26″ E, alt. 763 m, 20 August 2019, coll. C.-L.H., J.-Q.L. and G.-Q.C. (BJTC C561).
Etymology: The epithet “yanshanensis” refers to the locality where the type specimen was collected.
Basidiomata: small to medium size, pileus 21–53 mm in diameter, initially hemispherical to convex when young, applanate with slightly depressed in the center when mature, not obvious striations or no striations in the margin, sticky when wet, peeling to 1/3 of the radius, margin light pink (#ffb6c1) to pink (#ffc0cb), sometimes red (#ff1a1a), central light yellow (#ffffed) to yellowish-brown (#aa8d6f). Lamellae: white (#ffffff) to light yellow-brown (#ffffed), with 6–9 gills per cm at the edges, free, brittle, unequal, lamellulae absent, hardly forked. Stipe: 31–60 × 10–20 mm, white (#ffffff), sometimes with brownish (#a52a2a) on the base, cylindrical, inflated toward the base, hollow, longitudinally striate. Context: 5–11 mm thick in half of the pileus radius, white (#ffffff), without color change when bruised. Spore print: not observed.
Basidiospores: (5.6–)6.1–6.6–7.1(–7.5) × (5.1–)5.5–5.8–6.1(–6.4) μm, [Q = (1.03–)1.07–1.14–1.21(–1.29)], subglobose to broadly ellipsoid, ornamentation of relatively small, dense [7–10(–11)] in a 3 μm diameter circle] amyloid warts, 0.2–0.6 μm high, occasionally with isolated warts, occasionally to frequently fused in short or long branched chains [(0–)1–3(–4) in the circle], frequently connected by short or long fine line connections [(0–)1–4(–5) in the circle], suprahilar spot not obvious, amyloid or weakly amyloid. Basidia: (34–)34.6–37.7–40.8(–47) × (11–)11.4–12.5–13.6(–15) μm, 2–4-spored, clavate, with particles and oil droplets, basidiola clavate or subcylindrical, ca. 8–13 μm wide. Hymenial cystidia: disperse, ca. 550/mm2. Hymenial cystidia on lamellae sides: (36–)37.5–50–62.5(–68) × (6.4–)7.1–8.3–9.5(–11) μm, thin-walled, clavate, subcylindricalor subfusiform, apically mainly obtuse, often with 2–4 μm long appendage; contents with heteromorphous-granulose or banded turning reddish brown (#a52a2a) in SV. Hymenial cystidia on lamellae edges: smaller to hymenial cystidia on lamellae sides, (30–)32.7–37.3–41.9(–45) × (7.0–)7.1–8–8.9(–9) μm, subclavate or fusiform, apically occasionally mucronate, sometimes with 2–7 μm long appendage, contents with heteromorphous-granulose or a few refractive, turning reddish brown (#a52a2a) in SV.
Marginal cells: (13.7–)14.6–17.3–19.9(–22.3) × (4.9–)5.7–6.5–7.2(–8.1) μm, cylindrical or ellipsoid. Pileipellis: orthochromatic in cresyl blue, sharply delimited from the underlying context, 50–80 μm deep, two-layered, less gelatinized. Suprapellis 40–60 μm deep, composed of ascending hyphae. Subpellis 20–35 μm deep, composed of horizontally oriented, intricate, 2–10 μm wide hyphae. Hyphal terminations near the pileus margin rarely branched, sometimes flexuous, thin-walled; terminal cells (13–)15.5–28.7–41.9(–52) × (2.0–)2.5–3.2–3.9(–4.1) μm, cylindrical, subfusiform, less lageniform, occasionally flexible, apically obtuse, sometimes attenuated or constricted, subterminal cells often wider, ca. 2–4 μm wide, always unbranched; hyphal terminations near the pileus center similar to those near the pileus margin; terminal cells (9.2–)10.4–19.4–28.4(–33.6) × (2.0–)2.2–3–3.8(–4.1) μm, mainly subcylindrical, less lageniform, apically obtuse; sometimes attenuated or constricted, subterminal cells often wider, always unbranched, ca. 2–4 μm wide. Pileocystidia near the pileus margin are always 2–3-celled, sometimes one-celled, thin-walled, sometimes subpellis extends to suprapellis, terminal cells (23.8–)25.6–39.4–53.2(–65.2) × (5.0–)5.4–7.6–8(–9.1) μm, cylindrical or clavate, apically usually obtuse; contents with abundant granulose or heteromorphous-crystalline, have weakly reaction turning light ash black (#0d0d0d) to light red (#ff4d4d) in SV. Pileocystidia near the pileus center simiar to the pileus margin, usually 2–3-celled, thin-walled, (20.2–)18.6–25.1–31.6(–39.8) × 6–6.7–9 μm, clavate, apically obtuse, contents with granulose or crystalline. Cystidioid hyphae: in subpellis and context with granulose or crystalline contents. Oleiferous hyphae in the subpellis.
Habit and habitat: Individual or scattered in coniferous or broad-leaved forests such as P. tabuliformis Carr., Betula costata Trautv. And Populus davidiana Dode trees.
Additional specimens examined: CHINA, Beijing, Huairou District, Sunzhazi Village, 40°56′40.5″ N, 116°30′25.2″ E, alt. 763 m, 20 August 2019, coll. C.-L.H., J.-Q.L. and G.-Q.C. (BJTC L349); CHINA, Beijing, Miyun District, Sileng Mountain, 40°28′23″ N, 117°6′17″ E, alt. 709 m, 30 August 2021, coll. C.-L.H., H.Z. and G.-Q.C. (BJTC Z1390); CHINA, Beijing, Miyun District, Sileng Mountain, 40°28′24″ N, 117°6′32″ E, alt. 663 m, 30 August 2021, coll. C.-L.H., H.Z. and G.-Q.C. (BJTC Z1385); CHINA, Beijing, Huairou District, Xiaozhuanghu Village, 40°52′35.6″ N, 116°31′16.6″ E, alt. 804 m, 20 August 2019, coll. H.Z. and X.-Y.S. (BJTC Z421); CHINA, Beijing, Huairou District, Sunzhazi Village, 40°56′35.6″ N, 116°30′26.0″ E, alt. 779 m, 25 August 2020, coll. C.-L.H., H.Z. and G.-Q.C. (BJTC C561); CHINA, Beijing, Yanqing District, Sijihuahai, 40°33′26″ N, 116°20′28″ E, alt. 733 m, 4 August 2021, coll. H.Z. and G.-Q.C. (BJTC Z1305); CHINA, Beijing, Yanqing District, Yudu Mountain, 40°33′5″ N, 115°52′15″ E, alt. 978 m, 31 August 2021, coll. C.-L.H., H.Z. and G.-Q.C. (BJTC Z1448).
Notes:Russula yanshanensis belongs to the subsection Puellarinae. Specimens of R. yanshanensis were placed in a high-support branch on the phylogenetic tree and probably related to R. puellaris (Figure 1 and Figure 2). Russula puellaris can be distinguished from R. puellaris by its thinner basidiospores (28–43 × 9–12 µm), larger hymenial cystidia on lamellae sides (40–85 × 8–12), and turning gray in SV [55]. Morphologically, compare with similar species without molecular data. Russula yanshanensis is easy to be confused with R. cremeirosea in the appearance of basidiomata, but R. cremeirosea has bigger basidiospores (8–11 × 7.5–10 μm), longer hymenial cystidia on lamellae sides (50–76 × 3–10 µm), hymenial cystidia on lamellae edges (42–48 × 7–9 µm) and without pileocystidia [61].

4. Discussion

The topological structure of the two trees of the nrITS phylogenetic analysis (Figure 1) and the nrLSU-rpb2-tef-1α-mtSSU phylogenetic analysis (Figure 2) are basically similar, but the Bayesian posterior probability values and maximum likelihood bootstrap were higher in the nrLSU-rpb2-tef-1α-mtSSU analysis. In recent studies, many new species of Russula have been described only by nrITS loci phylogenetic analysis [14,25,62], which also results in the lack of other gene sequences and may cause some difficulties when performing multi-gene phylogenetic analysis. Therefore, it is crucial to discover better-differentiated DNA barcodes within the subgenus Russula in subsequent studies.
Through the current investigation, most species of the Russula were found in broad-leaved forests and associated with Carpinus turczaninowii, Castanea mollissima, J. mandshurica, B. costata, and P. davidiana trees, few species of the Russula occurred in coniferous forests, such as P. tabuliformis. The distributing characteristics may be related to the large area of broad-leaved forest in the Yanshan Mountains.
Russula Subgenus Russula has a very high species richness worldwide. At least 50 novel species have been described based on both morphological characters and molecular data since 2006, of which at least 30 species were reported from Asia [35]. In previous research, 16 species of Russula subgenus Russula are reported from southern China. [9,18,23,32,33,34,35,63,64]. Moreover, six species are from Northeast China [18,24,65,66]. Regarding the provincial distribution in China, more species of subgenus Russula are found in Guangdong Province and Heilongjiang Province. The reason for this phenomenon may be that these two provinces are actively investigated by mycologists.
In this study, six new species belonged to three subsections under the subgenus Russula, namely subsection Chamaeleontinae (R. miyunensis and R. plana), subsection Puellarinae (R. sinoparva, R. sinorobusta, and R. yanshanensis) and subsection Roseinae (R. subversatilis). Subsection Chamaeleontinae belongs to species of normally small size. The cap is not much fleshy, the cuticle is detachable, and the margin is smooth or just grooved, especially when ripe; the stem is white, frail, and meaty, then hollow. Two new species, R. miyunensis and R. plana, described in this study, also fit these characteristics. Referring to Sarnari’s classification system, subsection Chamaeleontinae belongs to section Amethystinae Romagn. [5], and the position of this group in the systematic tree is also relatively stable. No Chinese Russula species belonging to subsection Chamaeleontinae have been identified in previous studies. Subsection Puellarinae was established by Singer in 1932 [67]. Singer had studied American and tropical Russulas prior to proposing his classification. Subsections Chamaeleontina Singer, Subcompactinae Singer, and Puellarinae were separated out within section Constantes Singer [68]. Russula khinganensis, described by Li et al., is also a member of subsection Puellarinae [24]. Subsection Roseinae was recognized by Sarnari in 1998 [5]. Morphologically, members of the subsection Roseinae provide a persistent bright red-colored reaction in dried fruit bodies with sulfovanilin. No species of subsection Roseinae were reported before among Russula species in China.
Russula contains a number of wild edible fungi in the world, and there are also a certain number of poisonous fungi. The classification of Russula is a difficult point in the classification of macrofungi [11]. Therefore, a classification study of the Russula is also essential to promote the study of edible species within the genus. According to incomplete statistics, 128 species of Russula are used as edible mushrooms in 28 countries worldwide [69]. Moreover, 78 edible species of Russula in China were recorded by Wu et al. [12], e.g., Russula delica Fr., Russula densifolia Secr. ex Gillet, Russula griseocarnosa X.H. Wang, Zhu L. Yang, & Knudsen.
Through literature review, all three subsections in which the six new species of this study are located have edible species distributed in China [70]. In subsection Chamaeleontinae, Russula turci Bres. and Russula roseipes Secr. ex Bres. are representative species. In subsection Puellarinae, Russula puellaris Fr. is a representative species and is more widely distributed in China. In subsection Roseinae, there are more edible mushrooms known in this subsection, including Russula pseudointegra Arnould & Goris, Russula rosea Pers., Russula lepidicolor Romagn., and all the above species are also distributed in China. Therefore, the six new species discovered this time should also contain edible species that worth to be studied.
This study is the first report of the species of Russula subgenus Russula from the Yanshan Mountains in northern Beijing and northern Hebei Province. Considering the large area of China and its diverse forest types, it is reasonable to infer that many more species of the genus Russula are expected to be found in the following studies. On the premise of determining the number of Russula species, relevant studies on edible species can be further deepened.

Author Contributions

C.-L.H. and H.Z. conceived and designed the study; H.Z., G.-Q.C. and G.-J.L. wrote the manuscript; G.-Q.C., H.Z. and Q.-T.W. conducted phylogenetic analysis and morphological observations; G.-Q.C., M.-J.G., H.-F.Y. and L.Z. conducted the experiments. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by The Biodiversity Survey and Assessment Project of the Ministry of Ecology and Environment, China (2019HJ2096001006) and the National Natural Science Foundation of China (No. 31870629).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

All sequence data are available in NCBI GenBank following the accession numbers in the manuscript.

Acknowledgments

Thanks to Li Fan, Capital Normal University, for providing experimental guidance and assistance with the writing of the manuscript. We thank the two anonymous reviewers for their constructive criticism and suggestions to improve our work.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 2. The nrLSU-rpb2-tef-1α-mtSSU multi-locus phylogenetic tree obtained from the Bayesian analysis. Numbers above branches represent strongly and moderately support (pp ≥ 0.95 and/or MLB ≥ 50%). Numbers above branches are Bayesian posterior probability (pp) values and maximum likelihood bootstrap (MLB). The red font indicates the position of newly obtained sequences. Accession numbers of sequences information used are indicated in Table 1. Asterisks (*) denote branches with pp = 1.00, MLb = 100%.
Figure 2. The nrLSU-rpb2-tef-1α-mtSSU multi-locus phylogenetic tree obtained from the Bayesian analysis. Numbers above branches represent strongly and moderately support (pp ≥ 0.95 and/or MLB ≥ 50%). Numbers above branches are Bayesian posterior probability (pp) values and maximum likelihood bootstrap (MLB). The red font indicates the position of newly obtained sequences. Accession numbers of sequences information used are indicated in Table 1. Asterisks (*) denote branches with pp = 1.00, MLb = 100%.
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Figure 3. Russula miyunensis (BJTC Z1355). (A–D) Basidiomata. (E,F) Basidiospores. Scale bar: (A–D) = 10 mm, (E,F) = 1 μm.
Figure 3. Russula miyunensis (BJTC Z1355). (A–D) Basidiomata. (E,F) Basidiospores. Scale bar: (A–D) = 10 mm, (E,F) = 1 μm.
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Figure 4. Microscopic features of Russula miyunensis (BJTC Z1355). (A) Basidia. (B) Basidiola. (C) Marginal cells. (D) Hymenial cystidia on lamellae sides. (E) Hymenial cystidia on lamellae edges. Scale bar: 10 μm.
Figure 4. Microscopic features of Russula miyunensis (BJTC Z1355). (A) Basidia. (B) Basidiola. (C) Marginal cells. (D) Hymenial cystidia on lamellae sides. (E) Hymenial cystidia on lamellae edges. Scale bar: 10 μm.
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Figure 5. Microscopic features of Russula miyunensis (BJTC Z1355). (A) Primordial hyphae near the pileus margin. (B) Hyphal terminations near the pileus margin. (C) Primordial hyphae near the pileus center. (D) Hyphal terminations near the pileus center. Scale bar: 10 μm.
Figure 5. Microscopic features of Russula miyunensis (BJTC Z1355). (A) Primordial hyphae near the pileus margin. (B) Hyphal terminations near the pileus margin. (C) Primordial hyphae near the pileus center. (D) Hyphal terminations near the pileus center. Scale bar: 10 μm.
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Figure 6. Microscopic features of Russula miyunensis (BJTC Z1355). (A) Basidiospores. (B) Hyphal terminations near the pileus margin. (C) Hyphal terminations near the pileus center. Scale bar: (A) = 5 μm; (B,C) = 10 μm.
Figure 6. Microscopic features of Russula miyunensis (BJTC Z1355). (A) Basidiospores. (B) Hyphal terminations near the pileus margin. (C) Hyphal terminations near the pileus center. Scale bar: (A) = 5 μm; (B,C) = 10 μm.
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Figure 7. Russula plana (BJTC Z1398). (A,B) Basidiomata. (C,D) Basidiospores. Scale bar: (A,B) = 10 mm, (C,D) = 1 μm.
Figure 7. Russula plana (BJTC Z1398). (A,B) Basidiomata. (C,D) Basidiospores. Scale bar: (A,B) = 10 mm, (C,D) = 1 μm.
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Figure 8. Microscopic features of Russula plana (BJTC Z1398). (A) Basidia. (B) Basidiola. (C) Marginal cells. (D) Hymenial cystidia on lamellae sides. (E) Hymenial cystidia on lamellae edges. Scale bar: 10 μm.
Figure 8. Microscopic features of Russula plana (BJTC Z1398). (A) Basidia. (B) Basidiola. (C) Marginal cells. (D) Hymenial cystidia on lamellae sides. (E) Hymenial cystidia on lamellae edges. Scale bar: 10 μm.
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Figure 9. Microscopic features of Russula plana (BJTC Z1398). (A) Primordial hyphae near the pileus margin. (B) Hyphal terminations near the pileus margin. (C) Primordial hyphae near the pileus center. (D) Hyphal terminations near the pileus center. Scale bar: 10 μm.
Figure 9. Microscopic features of Russula plana (BJTC Z1398). (A) Primordial hyphae near the pileus margin. (B) Hyphal terminations near the pileus margin. (C) Primordial hyphae near the pileus center. (D) Hyphal terminations near the pileus center. Scale bar: 10 μm.
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Figure 10. Microscopic features of Russula plana (BJTC Z1398). (A) Basidiospores. (B) Hyphal terminations near the pileus margin. (C) Hyphal terminations near the pileus center. Scale bar: (A) = 5 μm; (B,C) = 10 μm.
Figure 10. Microscopic features of Russula plana (BJTC Z1398). (A) Basidiospores. (B) Hyphal terminations near the pileus margin. (C) Hyphal terminations near the pileus center. Scale bar: (A) = 5 μm; (B,C) = 10 μm.
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Figure 11. Russula sinoparva (BJTC ZH441). (A,B) Basidiomata. (C,D) Basidiospores. Scale bar: (A,B) = 10 mm, (C,D) = 5 μm.
Figure 11. Russula sinoparva (BJTC ZH441). (A,B) Basidiomata. (C,D) Basidiospores. Scale bar: (A,B) = 10 mm, (C,D) = 5 μm.
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Figure 12. Microscopic features of Russula sinoparva (BJTC ZH441). (A) Basidia. (B) Basidiola. (C) Marginal cells. (D) Hymenial cystidia on lamellae sides. Scale bar: 10 μm.
Figure 12. Microscopic features of Russula sinoparva (BJTC ZH441). (A) Basidia. (B) Basidiola. (C) Marginal cells. (D) Hymenial cystidia on lamellae sides. Scale bar: 10 μm.
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Figure 13. Microscopic features of Russula sinoparva (BJTC ZH441). (A) Pileocystidia near the pileus margin. (B) Hyphal terminations near the pileus margin. (C) Pileocystidia near the pileus center. (D) Hyphal terminations near the pileus center. Scale bar: 10 μm.
Figure 13. Microscopic features of Russula sinoparva (BJTC ZH441). (A) Pileocystidia near the pileus margin. (B) Hyphal terminations near the pileus margin. (C) Pileocystidia near the pileus center. (D) Hyphal terminations near the pileus center. Scale bar: 10 μm.
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Figure 14. Microscopic features of Russula sinoparva (BJTC ZH441). (A) Basidiospores. (B) Hyphal terminations near the pileus margin. (C) Hyphal terminations near the pileus center. Scale bar: (A) = 5 μm; (B,C) = 10 μm.
Figure 14. Microscopic features of Russula sinoparva (BJTC ZH441). (A) Basidiospores. (B) Hyphal terminations near the pileus margin. (C) Hyphal terminations near the pileus center. Scale bar: (A) = 5 μm; (B,C) = 10 μm.
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Figure 15. Russula sinorobusta (BJTC Z052). (A–D) Basidiomata. (E,F) Basidiospores. Scale bar: (A–D) = 10 mm, (E,F) = 1 μm.
Figure 15. Russula sinorobusta (BJTC Z052). (A–D) Basidiomata. (E,F) Basidiospores. Scale bar: (A–D) = 10 mm, (E,F) = 1 μm.
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Figure 16. Microscopic features of Russula sinorobusta (BJTC Z052). (A) Basidia. (B) Basidiola. (C) Marginal cells. (D). Hymenial cystidia on lamellae sides. (E) Hymenial cystidia on lamellae edges. Scale bar: 10 μm.
Figure 16. Microscopic features of Russula sinorobusta (BJTC Z052). (A) Basidia. (B) Basidiola. (C) Marginal cells. (D). Hymenial cystidia on lamellae sides. (E) Hymenial cystidia on lamellae edges. Scale bar: 10 μm.
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Figure 17. Microscopic features of Russula sinorobusta (BJTC Z052). (A) Hyphal terminations near the pileus margin. (B) Hyphal terminations near the pileus center. Scale bar: 10 μm.
Figure 17. Microscopic features of Russula sinorobusta (BJTC Z052). (A) Hyphal terminations near the pileus margin. (B) Hyphal terminations near the pileus center. Scale bar: 10 μm.
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Figure 18. Microscopic features of Russula sinorobusta (BJTC Z052). (A) Basidiospores. (B) Hyphal terminations near the pileus margin. (C) Hyphal terminations near the pileus center. Scale bar: (A) = 5 μm; (B,C) = 10 μm.
Figure 18. Microscopic features of Russula sinorobusta (BJTC Z052). (A) Basidiospores. (B) Hyphal terminations near the pileus margin. (C) Hyphal terminations near the pileus center. Scale bar: (A) = 5 μm; (B,C) = 10 μm.
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Figure 19. Russula subversatilis (BJTC C653). (A,B) Basidiomata. (C,D) Basidiospores. Scale bar: (A,B) = 10 mm, (C,D) = 1 μm.
Figure 19. Russula subversatilis (BJTC C653). (A,B) Basidiomata. (C,D) Basidiospores. Scale bar: (A,B) = 10 mm, (C,D) = 1 μm.
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Figure 20. Microscopic features of Russula subversatilis (BJTC C653). (A) Basidia. (B) Basidiola. (C) Marginal cells. (D) Hymenial cystidia on lamellae sides. (E) Hymenial cystidia on lamellae edges. Scale bar: 10 μm.
Figure 20. Microscopic features of Russula subversatilis (BJTC C653). (A) Basidia. (B) Basidiola. (C) Marginal cells. (D) Hymenial cystidia on lamellae sides. (E) Hymenial cystidia on lamellae edges. Scale bar: 10 μm.
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Figure 21. Microscopic features of Russula subversatilis (BJTC C653). (A) Pileocystidia near the pileus margin. (B) Hyphal terminations near the pileus margin. (C) Pileocystidia near the pileus center. (D) Hyphal terminations near the pileus center. Scale bar: 10 μm.
Figure 21. Microscopic features of Russula subversatilis (BJTC C653). (A) Pileocystidia near the pileus margin. (B) Hyphal terminations near the pileus margin. (C) Pileocystidia near the pileus center. (D) Hyphal terminations near the pileus center. Scale bar: 10 μm.
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Figure 22. Microscopic features of Russula subversatilis (BJTC C653). (A) Basidiospores. (B) Hyphal terminations near the pileus margin. (C) Hyphal terminations near the pileus center. Scale bar: (A) = 5 μm; (B,C) = 10 μm.
Figure 22. Microscopic features of Russula subversatilis (BJTC C653). (A) Basidiospores. (B) Hyphal terminations near the pileus margin. (C) Hyphal terminations near the pileus center. Scale bar: (A) = 5 μm; (B,C) = 10 μm.
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Figure 23. Russula yanshanensis (BJTC C561). (A,B) Basidiomata. (C,D) Basidiospores. Scale bar: (A,B) = 10 mm, (C,D) = 1 μm.
Figure 23. Russula yanshanensis (BJTC C561). (A,B) Basidiomata. (C,D) Basidiospores. Scale bar: (A,B) = 10 mm, (C,D) = 1 μm.
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Figure 24. Microscopic features of Russula yanshanensis (BJTC C561). (A) Basidia. (B) Basidiola. (C) Marginal cells. (D) Hymenial cystidia on lamellae sides. (E) Hymenial cystidia on lamellae edges. Scale bar: 10 μm.
Figure 24. Microscopic features of Russula yanshanensis (BJTC C561). (A) Basidia. (B) Basidiola. (C) Marginal cells. (D) Hymenial cystidia on lamellae sides. (E) Hymenial cystidia on lamellae edges. Scale bar: 10 μm.
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Figure 25. Microscopic features of Russula yanshanensis (BJTC C561). (A) Pileocystidia near the pileus margin. (B) Hyphal terminations near the pileus margin. (C) Pileocystidia near the pileus center. (D) Hyphal terminations near the pileus center. Scale bar: 10 μm.
Figure 25. Microscopic features of Russula yanshanensis (BJTC C561). (A) Pileocystidia near the pileus margin. (B) Hyphal terminations near the pileus margin. (C) Pileocystidia near the pileus center. (D) Hyphal terminations near the pileus center. Scale bar: 10 μm.
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Figure 26. Microscopic features of Russula yanshanensis (BJTC C561). (A) Basidiospores. (B) Hyphal terminations near the pileus margin. (C) Hyphal terminations near the pileus center. Scale bar: (A) = 5 μm; (B,C) = 10 μm.
Figure 26. Microscopic features of Russula yanshanensis (BJTC C561). (A) Basidiospores. (B) Hyphal terminations near the pileus margin. (C) Hyphal terminations near the pileus center. Scale bar: (A) = 5 μm; (B,C) = 10 μm.
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Table
Table 1. Sequences information used in the nrLSU-rpb2-tef-1α-mtSSU phylogenetic analysis in this study.
Table 1. Sequences information used in the nrLSU-rpb2-tef-1α-mtSSU phylogenetic analysis in this study.
TaxaVoucherLocationGenBank Accession Numbers
nrLSUmtSSUrpb2tef-1α
Multifurca aurantiophylla644/BB 09.119New CaledoniaKU237581KU237429KU237867KU238008
Multifurca ochricompacta580/BB 07.010USAKU237565KU237413KU237851KU237994
Russula abbottabadensisLAH 310071PakistanMN518356MG386719MG386737MZ364137
Russula abbottabadensisFH 00304558PakistanMN518355MG386721MG386738MZ364138
Russula acrifolia543/BB 08.662ItalyKU237535KU237381KU237821KU237965
Russula adusta223/BB 06.562CanadaKU237476KU237320KU237762KU237907
Russula amethystina529/BB 07.314SlovakiaKU237521KU237367KU237807KU237951
Russula archaeosuberis1118/BB 12.085ItalyKU237593KU237441KU237878KU238019
Russula ayubianaLAH 35438PakistanMZ358816MZ364121MZ364131MZ364139
Russula ayubianaLAH 35439PakistanMZ358817MZ364122MZ364132MZ364140
Russula azurea537/BB 08.668ItalyKU237529KU237375KU237815KU237959
Russula betularumBPL269USAKT933829KT933969KT933900-
Russula bicolorHMJAU 32180ChinaKX095080KX095031--
Russula brevipes226/BB 06.508MexicoKU237479KU237323KU237765-
Russula burlinghamiae548/BB 05.108USAKU237540KU237386KU237826KU237970
Russula carpini551/BB 07.262SlovakiaKU237543KU237389KU237829KU237973
Russula chloroides572/BB 07.209SlovakiaKU237559KU237407KU237845KU237990
Russula compacta228/BB 06.295USAKU237480KU237324KU237766-
Russula corallina-229/BB 06.324USAKU237481KU237325KU237767KU237910
Russula crustosaBPL265USAKT933826-KT933898-
Russula cuprea565/BB 07.233SlovakiaKU237555KU237401KU237841KU237984
Russula decolorans549/BB 07.322SlovakiaKU237541KU237387KU237827KU237971
Russula emetica635/JMT39-08092228FranceKU237578KU237426KU237864-
Russula exalbicans584/BB 07.786FranceKU237568KU237416KU237854KU237996
Russula farinipes576/BB 08.632ItalyKU237561KU237409KU237847KU237992
Russula fattoensisBuyck 02.227USAMN315514MN315537MN326797MN326800
Russula fragilis443/BB 07.791FranceKU237506KU237351KU237792-
Russula glutinosaRoody WRWV 04.1154USAMN315511MN315532MN326798MN326799
Russula gracillima441/BB 07.785FranceKU237504KU237349KU237790KU237934
Russula griseobrunneaJAC11227New ZealandMW683630
Russula herrerae239/BB 06.532MexicoKU237486KU237330KU237772KU237915
Russula integra518/BB 07.198SlovakiaKU237513KU237359KU237799KU237943
Russula laeta519/BB 07.267SlovakiaKU237514KU237360KU237800KU237944
Russula laricina575/BB 08.681ItalyKU237560KU237408KU237846KU237991
Russula leucomarginataRITF3133ChinaMW309327MW309338MW310568-
Russula leucomarginataRITF3123ChinaMW309328MW309339MW310569-
Russula lilacea435/BB 07.213SlovakiaKU237498KU237343KU237784KU237928
Russula mansehraensisHUP SUR 180PakistanMG944280MG944266MG944255-
Russula mansehraensisHUP SUR 803Pakistan-MG944267MG944256-
Russula minutula539/BB 08.636ItalyKU237531KU237377KU237817KU237961
Russula miyunensisBJTC Z1357China-OP135984OP156826OP156837
Russula miyunensisBJTC Z1355ChinaOP133232OP135985OP156827-
Russula mustelina1176/SA 09.88SlovakiaKU237596KU237444KU237881KU238022
Russula nauseosa588/BB 07.285ItalyKU237572KU237420KU237858KU238000
Russula nigricans429/BB 07.342SlovakiaKU237495KU237339KU237781KU237924
Russula nothofagineae723/BB 09.044New CaledoniaKU237583KU237431-KU238010
Russula nothofagineae726/BB 09.069New CaledoniaKU237585KU237433KU237870KU238012
Russula odorata526/BB 07.186SlovakiaKU237518KU237364KU237804KU237948
Russula olivascens530/BB 08.663ItaliaKU237522KU237368KU237808KU237952
Russula olivobrunneaJV28388Finland-MW633232--
Russula planaBJTC Z1398ChinaOP133233OP135986OP156828OP156838
Russula planaBJTC T2101ChinaOP265903OP265901OP267556OP267558
Russula pseudoaurantiophylla740/BB 09.219New CaledoniaKU237591KU237439KU237876KU238017
Russula puellaris523/BB 07.311SlovakiaKU237515KU237361KU237801KU237945
Russula purpureoverrucosaGDGM32902ChinaMG214699-MT085652MT085623
Russula quercus-floribundaeLAH 36219PakistanMN513043MN053397MN053389MZ364152
Russula quercus-floribundaeLAH 36220PakistanMN513043MN053396MN053390MZ364153
Russula raoultii561/BB 08.674ItalyKU237551KU237397KU237837KU237980
Russula rosea430/BB 07.780FranceKU237496KU237340KU237782KU237925
Russula roseolaRITF3418ChinaMW309319MW309330MW310560-
Russula roseolaRITF3428ChinaMW309320MW309331MW310561-
Russula sinoparvaBJTC C540ChinaOP133234OP135987OP156829OP156839
Russula sinoparvaBJTC Z441ChinaOP133235OP135988-OP156840
Russula sinorobustaBJTC Z050ChinaOP133236OP135989OP156830OP156841
Russula sinorobustaBJTC Z052China-OP135990-OP156842
Russula sinorobustaBJTC Z662ChinaOP133237OP135991OP156831OP156843
Russula sichuanensisZRL20162017ChinaMG786572MG792323-MG812160
Russula solaris559/BB 07.282SlovakiaKU237549KU237395KU237835KU237978
Russula sp.735/BB 09.172New CaledoniaKU237588KU237436KU237873KU238015
Russula subsanguinariaRITF2236ChinaMW309322MW309333MW310563-
Russula subsanguinariaRITF2208ChinaMW309323MW309334MW310564-
Russula subtilis536/BB 05.107USAKU237528KU237374KU237814KU237958
Russula subversatilisBJTC C653ChinaOP133238OP135992OP156832OP156844
Russula subversatilisBJTC T2001ChinaOP265904OP265902OP267557OP267559
Russula turci528/BB 07.328SlovakiaKU237520KU237366KU237806KU237950
Russula versicolor589/BB 07.288SlovakiaKU237573KU237421KU237859KU238001
Russula vinosobrunneolaHMAS 281138ChinaMG786569MG792320-MG812157
Russula vinosobrunneolaHMAS 278885ChinaMG786570MG792321-MG812158
Russula yanshanensisBJTC C561ChinaOP133239OP135993-OP156845
Russula yanshanensisBJTC Z1448ChinaOP133240OP135994OP156833-
Russula yanshanensisBJTC Z421ChinaOP133241OP135995-OP156846
Russula yanshanensisBJTC Z1385ChinaOP133242OP135996-OP156847
Russula yanshanensisBJTC Z1305ChinaOP133243OP135997OP156834OP156848
Russula yanshanensisBJTC Z1390ChinaOP133244OP135998OP156835OP156849
Russula yanshanensisBJTC L349ChinaOP133245OP135999OP156836OP156850
Russula zvarae538/BB 08.639ItalyKU237530KU237376KU237816KU237960
Remarks: The new generated sequences are emphasized in bold, “-” show no sequence. Database.
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Zhou, H.; Cheng, G.-Q.; Wang, Q.-T.; Guo, M.-J.; Zhuo, L.; Yan, H.-F.; Li, G.-J.; Hou, C.-L. Morphological Characteristics and Phylogeny Reveal Six New Species in Russula Subgenus Russula (Russulaceae, Russulales) from Yanshan Mountains, North China. J. Fungi 2022, 8, 1283. https://doi.org/10.3390/jof8121283

AMA Style

Zhou H, Cheng G-Q, Wang Q-T, Guo M-J, Zhuo L, Yan H-F, Li G-J, Hou C-L. Morphological Characteristics and Phylogeny Reveal Six New Species in Russula Subgenus Russula (Russulaceae, Russulales) from Yanshan Mountains, North China. Journal of Fungi. 2022; 8(12):1283. https://doi.org/10.3390/jof8121283

Chicago/Turabian Style

Zhou, Hao, Gui-Qiang Cheng, Qiu-Tong Wang, Mei-Jun Guo, Lan Zhuo, Hui-Fang Yan, Guo-Jie Li, and Cheng-Lin Hou. 2022. "Morphological Characteristics and Phylogeny Reveal Six New Species in Russula Subgenus Russula (Russulaceae, Russulales) from Yanshan Mountains, North China" Journal of Fungi 8, no. 12: 1283. https://doi.org/10.3390/jof8121283

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