Research Article
Research Article
Two new species of Hygrophorus from temperate Himalayan Oak forests of Pakistan
expand article infoArooj Naseer, Abdul Nasir Khalid, Rosanne Healy§, Matthew E. Smith§
‡ University of the Punjab, Lahore, Pakistan
§ University of Florida, Gainesville, United States of America
Open Access


The genus Hygrophorus is poorly studied from Asia. From Pakistan, only one species has been reported so far. Two new species in the genus have been collected from Himalayan oak forests of Pakistan. Hygrophorus alboflavescens (section Pudorini, subgenus Colorati) is characterised by its pure white, centrally depressed pileus, occurrence of white stipe with yellow patches at lower half and broader (4.98 μm) basidiospores. Hygrophorus scabrellus (section Hygrophorus, subgenus Hygrophorus) is characterised by its yellowish-green stipe with white apex that has fine scales on the entire stipe, an off-white pileus with dark green and greyish fibrils, ovoid to ellipsoid basidiospores and clavate 4-spored basidia. Macro- and micromorphological descriptions have revealed that both these taxa are not yet described. Phylogenetic estimation based on DNA sequences from the internal transcribed spacer (ITS) region and large subunit (LSU) of the nuclear ribosomal DNA (rDNA) genes, is congruent with the morphological characters that help to delimit these as new species of Hygrophorus. Allied taxa are also compared.


Biodiversity, Community structure, Dir, ECM, Shawar Valley


The genus Hygrophorus Fr. (Hygrophoraceae, Agaricales) is one of the ectomycorrhizal (ECM) genera in Agaricales. The genus name Hygrophorus Fr. (Hygrophoraceae, Agaricales) comes from hygro meaning moisture and phorus meaning bearer. This may refer to the glutinous to viscid pileus character that many of these fungi have due to a layer of gel that makes them sticky to touch when moist. The genus is characterised by diverse basidiomata colours, basidiomata which are tricholomatoid, collybioid, clitocyboid or omphalinoid, lamellae that are subdecurrent, spores that are smooth and hyaline and a hymenium without cystidia. Basidiomata in this group vary from small to large; thin to fleshy; dry to very glutinous or viscid pileus; with a dry to glutinous, glabrous or fibrillose, generally pruinose or granulose stipe (Singer 1986; Bas et al. 1990; Boertmann 1995; Young 2005; Kovalenko 2012). Colour of the pileus is a characteristic feature in the classification of Hygrophorus especially at the level of subsection (Hesler and Smith 1963). Sect. Hygrophorus has white to cream basidiomata while taxa with colourful basidiomata are in different sections and subsections (Fries 1874; Singer 1943; Candusso 1997).

The family Hygrophoraceae Lotsy was revised by Lodge et al. (2014) on the basis of integrated molecular phylogeny, morphological analyses, pigment chemistry and ecology. They classified the family with three new subfamilies, eight tribes, eight subgenera, 26 sections and 14 subsections. Subgenus Colorati of genus Hygrophorus contain coloured mushrooms. In the new classification, the subg. Colorati (Bataille) E. Larss. has been divided into three sections: Olivaceoumbrini (Bataille) Konrad & Maubl., Pudorini (Bataille) Konrad & Maubl. and Aurei (Bataille) E. Larss. In addition, the section Pudorini is divided into two subsections: Clitocyboides and Pudorini. The subgenus Hygrophorus is divided into two sections: Hygrophorus and Fulventes.

Hygrophorus species are globally distributed and mostly occur in woodlands and forests with pines or with ectomycorrhizal (ECM) angiosperms (Bas et al. 1990). Hygrophorus are essential components of ECM communities of temperate regions in the Northern Hemisphere (Tedersoo et al. 2010). Recently, a new edible species, H. parvirussula has been described from south-western China (Huang et al. 2018) and it belongs to Hygrophorus section Pudorini. A few studies on the genus have been performed in Pakistan. Only one species, Hygrophorus chrysodon, was reported as a new record by Razaq et al. (2014), from the western Himalayan forests of Pakistan. Here we present two new species of Hygrophorus based on both morphology and molecular phylogeny.

Materials and methods

Morpho-anatomical analyses

Collections were made during field investigations for ECM communities associated with the oaks of Swat and Dir districts, Khyber Pakhtunkhwa province, Pakistan during 2014–2016. Basidiomata were found in a pure Quercus forest from Shawar Valley, Swat that is representative of the western Himalayan Province (Naseer et al. 2017b) and from Toa, Alpurai forests (Naseer et al. 2017), Swat, KP, Pakistan. The ECM roots were collected from the same forests as well as Biar, Upper Dir, KP, Pakistan. Biar is located in moist parts of dry temperate zones and it has Q. baloot as the leading species (89.44%) with Q. dilatata (10.46%). Basidiomata were collected following Lodge et al. (2014) and photographed in their natural habitats using a Nikon D70S camera. Morphological characters were recorded from fresh specimens. Colours were designated with reference to mColorMeter application (Yanmei He, Mac App Store). Specimens were deposited in the Herbarium, Department of Botany, University of the Punjab, Lahore, Pakistan (LAH) and the University of Florida Fungal Herbarium, Gainesville FL, USA (FLAS).

Microscopic characters are based on freehand sections from fresh and dried specimens mounted in 5% (w/v) aqueous potassium hydroxide (KOH) solution. Tissues from lamellae, pileipellis and stipitipellis were mounted in phloxine (1%) for better contrast and examined using a Meiji Techno MX4300H compound microscope.

A total of thirty basidiospores, basidia, cystidia and hyphae were measured from each collection. For basidiospores, the abbreviation “n/m/p” indicates n basidiospores measured from m fruit bodies of p collections. Dimensions for basidiospores are given using length × width (L × W) and extreme values are given in parentheses. The range contains a minimum of 90% of the values. Measurements include arithmetic mean of spore length and width for all spores measured, Q means spore length divided by spore width and avQ indicates average Q of all spores ± standard deviation.

Molecular analyses

Genomic DNA was extracted from basidioma gills following a modified CTAB extraction method (Bruns 1995) and from ectomycorrhizal roots by Extract-N-AmpTM Kit (Sigma- Aldrich, St Louis, MO, USA). ITS and LSU regions of nuclear rDNA were amplified using the pairs of primers ITS1F-ITS4B and LR0R-LR5 (Vilgalys and Hester 1990, White et al. 1990, Gardes and Bruns 1993). Polymerase chain reactions (PCR) were performed in 25 μl volume reactions. Visualisation of PCR products were accomplished using SYBR Green and 1.5% agarose gels with TAE buffer for gel electrophoresis. Successful amplicons were purified by enzymatic purification using Exonuclease I and Shrimp Alkaline Phosphatase enzymes (Werle et al. 1994). Purified products were sequenced by the University of Florida’s Interdisciplinary Center for Biotechnology Research ( Sequence chromatograms were trimmed, edited and assembled using Sequencher 4.1 (GeneCodes, Ann Arbor, MI). Once sequences were assembled and edited, they were deposited in GenBank (

Consensus sequences for ITS and LSU were used to query GenBank and the UNITE database using BLAST searches. Representative sequences from across the genus Hygrophorus were downloaded and imported into an alignment in Bioedit (Hall 1999). Sequences from ECM roots were also included in the ITS alignment. Cantharocybe gruberi (JN006422, DQ200927) sequences were chosen to root the phylogenetic trees following Razaq et al. (2014). Sequences were aligned with the programme MUSCLE (Edgar 2004). Maximum likelihood analyses for individual gene regions were performed via CIPRES Science Gateway (Miller et al. 2010) employing RAxML-HPC v.8. Rapid bootstrap analysis for the best-scoring ML tree was configured for each dataset. For the bootstrapping phase, the GTRCAT model was selected. One thousand rapid bootstrap replicates were run. A bootstrap proportion of ≥ 70% was considered significant.


Molecular phylogenetic analyses

Consensus sequences for the ITS region of H. alboflavescens were 601–638 bp after trimming. BLAST searches in NCBI and UNITE revealed 91% similarity to Hygrophorus penarioides Jacobsson & Larss. (EF395370, EF395371, EF395372 & UDBO1556) from Sweden (99% query cover, 0.0 E value). The two ITS sequences from ECM root tips of Q. incana from same forest (Shawar Valley) matched with Hygrophorus alboflavescens fruiting body sequences and these are depicted in the phylogenetic tree (Fig. 5).

The consensus sequence for the LSU region of H. alboflavescens was 780 bp after trimming. Initial BLAST analysis revealed it as 94% similar to H. sordidus Peck. (AF042562) from the USA and H. russula (Schaeff. ex Fr.) Kauffman, (AY586663) from Sweden (100% query, 0.0E value).

The ITS analysis revealed that sequences from Hygrophorus alboflavescens clustered with H. penarioides and H. sordidus with moderate bootstrap support within section Pudorini of subgenus Colorati. The LSU based phylogram showed that H. alboflavescens clustered with H. sordidus (Fig. 5). LSU sequences for H. penarioides were not available.

The consensus sequences for the ITS region of Hygrophorus scabrellus nom. prov. were 603–604 bp. BLAST results revealed that these sequences were 89% similar to Hygrophorus eburneus (Bull.) Fr. (AY463485, AY463484 & AY242855) with 100% query coverage. The consensus sequences also showed 87% similarity to H. cossus (Sowerby) Fr. as H. quercetorum P.D. Orton, which has been synonymised with H. cossus (Larsson and Jacobsson 2004) (AY463489) and H. cossus (AY242852) from Sweden with 100% query coverage and 0.0 E value.

The consensus sequence for the LSU region of Hygrophorus scabrellus was 763 bp. BLAST results revealed that these sequences were 96% similar to Hygrophorus cossus (AY548963 & KF381555) with 100% query coverage.

The H. scabrellus LSU sequences clustered with high bootstrap support with similar taxa in the section Hygrophorus of subgenus Hygrophorus (Fig. 6). In both our LSU and ITS analyses, H. scabrellus formed a sister lineage to H. cossus from Sweden with strong bootstrap support (Figs 5, 6).

Hygrophorus alboflavescens basidiomata were collected from Shawar Valley. Its ECM roots were collected from the same valley. The species falls into Hygrophorus, subgenus Colorati, section Pudorini and subsection Clitocyboides. Hygrophorus scabrellus clusters within subsect. Hygrophorus, section Hygrophorus of subgenus Hygrophorus. Some of the ECM root sequences clustered with H. pudorinus sequences (FJ845408) from Canada and H. pudorinus (KT875016) from Mexico in the phylogenetic tree (Fig. 5). H. pudorinus belongs to Subgenus Colorati, section Pudorinii 2, subsection Pudorini. The collection of this ECM is the first report of this species from Pakistan.


Hygrophorus alboflavescens A. Naseer & A.N. Khalid, sp. nov.

MycoBank No: MB828146
Figures 1, 2


Hygrophorus alboflavescens can be distinguished from related species by its white, centrally depressed pileus having yellow dots, with straight, even margins; occurrence of white stipe with yellow patches at lower half and broader (4.98 μm) basidiospores.

Figure 1. 

Morphology of Hygrophorus alboflavescens (Holotype). A–D Basidiomata A, B LAH35244; FLAS-F-59457 C, D LAH35243. Scale bar: 1.5 cm.

Figure 2. 

Anatomy of Hygrophorus alboflavescens. A–D LAH35243 (holotype) A Basida B Basidiospores C Pileipellis D Stipitipellis. Scale bars: 2.0 μm (A); 4.5 μm (B); 13.7 μm (C); 7.8 μm (D).


PAKISTAN. Khyber Pakhtunkhwa Province, Swat, Shawar Valley, 2100 m alt., solitary or in pairs, on soil under Quercus incana, 14 July 2014, Arooj Naseer & Abdul Nasir Khalid, ASSW36 (holotype: LAH35243).


The species epithet refers to the white pileus with yellow dots and white stipe with yellow patches.

Basidiomata medium to large sized. Pileus 7–10.5 cm in diameter, butter white (0.1B 8.8/0.3) with yellow (5.2Y 4.3/4) dots, plane, centrally depressed, context moderately thick, margin, even, smooth, straight, sometime incurved. Lamellae white (5.1GY 7.9/1.9) with yellow (6.1 Y 6.8/5.5) and pink (2.8Y 6.9/3.9) colouration, decurrent, thick, distant, L = 30–41, even, entire. Lamellulae irregular, of variable length, alternating with lamellae. Stipe 1.5–2.5 cm thick at apex, 0.5–1.5 cm at base, 8 –12.5 cm long, white (0.1B 8.8/0.3) with yellow (5.4Y 5.3/4) patches at lower half, cylindrical, slightly tapering at base, central, hollow.

Basidiospores [60/3/2] (5.52–) 5.6–7.9 (–8.1) × (3.84–) 3.9–6.5 (–6.7), avL × avW = 6.64 × 4.98, Q = (1.20–) 1.21 × 1.40 (–1.43), avQ = 1.34, light green to hyaline in 5% KOH, ellipsoid, oblong, thick-walled. Basidia 31.6–48.8 × 5.8–6.7 μm, hyaline in 5% KOH, four-spored, clavate with long sterigmata (up to 3.0–4.2 μm), densely guttulated. Hymenophoral Trama 4–5.2 μm in diameter, thin-walled, branched, septate, oil contents, clamp connection present. Pileipellis an ixocutis of wide, thick hyphae, 3.0–5.5 μm in diameter. Stipitipellis a cutis of parallel and erect hyphae, 3.1–5.3 μm in diameter, light yellow in 5% KOH, septate. Clamp Connections present in all tissues.

Habit and distribution

Solitary and in pairs on soil under Quercus incana, at 2100 m a.s.l., in thick moist temperate forest of the western Himalaya.

Additional material examined

PAKISTAN, Khyber Pakhtunkhwa province, Swat, Shawar Valley, 2100 m a.s.l., solitary or in a pair, on soil under Quercus incana, 14 July 2014, Arooj Naseer & Abdul Nasir Khalid, ASSW81 (LAH35244; FLAS-F-59457).


Hygrophorus alboflavescens nom. prov. can be distinguished from closely related species by the following combination of characters: a white, plane, centrally depressed pileus having straight margins; stipe that is white above and yellow below; and broadly ellipsoid spores. The closely related species Hygrophorus penarioides is also an oak-specific species (Table 1). However, they differ morphologically. Hygrophorus penarioides can easily be distinguished by its convex pileus with broad umbo and its involute margins (Jacobsson and Larsson 2007), whereas H. alboflavescens has centrally depressed pileus (without umbo) and straight margins. Hygrophorus penarioides has a pure white pileus and stipe which become cream or slightly pinkish with age, whereas H. alboflavescens has a white stipe and pileus with yellow colouration on both. Hygrophorus alboflavescens has a longer stipe (8–12.5 cm) and broader spores (3.9–6.7 μm) as compared to H. penarioides. Hygrophorus alboflavescens is further differentiated from closely related taxa, H. sordidus, which has a convex, expanded to plane pileus that is larger (8–20 cm broad) compared with the smaller (7–10.5 cm broad), centrally depressed pileus of H. alboflavescens. Hygrophorus alboflavescens has even, smooth and straight margins that differ from involute and subnoccose margins of H. sordidus. Molecular analyses based on ITS and LSU regions also support H. alboflavescens as a distinct taxon and demonstrate its ECM relationship with oak in Pakistan.

Table 1.

Comparsion of Hygrophorus spp. from Pakistan with morphologically similar species.

Characters/ Species H. alboflavescens sp. nov. H. penarioides Jacobsson & E. Larss. H. sordidus Peck H. scabrellus sp. nov. H. eburneus (Bull.) Fr. H. cossus (Sowerby) Fr.
Shape Centrally depressed Convex Convex, expand to plane Plano convex Obtuse to convex Broadly convex to nearly plane
Colour Pure white with yellow dots Pure white with creamy centre Pure white or rarely tinged yellowish buff Off-white with dark green White Pale orchraceous grey
Size 7–10.5 cm 9–15 cm 8–20 cm 2.4–2.8 cm 2–7(10) cm 3–7 cm
Umbo No umbo Broad umbo No umbo No Umbo Umbonate Obtuse nearly plane
Margins Even, smooth, straight, sometime incurved Strongly involute Involute and subnoccose Even, smooth, incurved Even, involute and floccose-pubescent Incurved
Surface Dry, yellow patches on lower half Finely floccose in uppermost part Dry, glabrous, upper portion obscurely noccose Scales on whole stipe Fine scales at apex only and rest of stipe is smooth Fibrillose-punctate to scabrous at apex, lower two-thirds covered by gelatinous sheath
Shape Cylindrical Strongly attenuated towards base Equal, sometimes attenuated towards base Cylindrical, finely scaled Equal/tapered downward/ with a greatly attenuated vermiform base, Equal, tapered at base
Colour White with yellow patches at lower half White, in lower part creamy White Yellowish-green with white apex White stipe Salmon-buff to cinnamon
Size 1.5–2.5 cm thick 8–12.5 cm long 15–35 mm thick 60–100 mm long 1.5–3.0 cm thick 6–10 cm long 0.3–0.5 cm thick 2.1–2.4 cm long 2–8(15) mm thick 4.5–15(18) cm long (3)8–12 mm thick 4–9 cm long
Size 6.64 × 4.98 μm 1.13–1.6 μm 6–8 × (3.5) 4–5.5 μm 6.5 × 3.84 μm 6–8(9) × 3.5–5 μm 7–9 × 4–4.5 μm
Shape Ellipsoid, oblong Broadly ellipsoid to ovoid Ellipsoid, smooth Ovoid to ellipsoid Ellipsoid, smooth Ellipsoid
Habitat Oak specific Oak specific Oak-hickory woods Oak specific Fagus specific Oak specific

Hygrophorus scabrellus A. Naseer & A.N. Khalid, sp. nov.

MycoBank No: MB828147
Figures 3, 4


Hygrophorus scabrellus is characterised by off-white, plano-convex pileus with greyish, dark green fibrils; yellowish-green, longer (2.1–2.4 cm) stipe with white apex and fine scales along the whole stipe; ovoid to ellipsoid, smooth and smaller (6.5 × 3.8 μm) basidiospores.

Figure 3. 

Morphology of Hygrophorus scabrellus. A, B Basidiomata. LAH35245 (holotype). Scale bars: 0.88 cm (A); 0.48 cm (B).

Figure 4. 

Anatomy of Hygrophorus scabrellus. A–H LAH35245 (holotype) A Basidia B Basidia with basidioles C Basidiospores D Cheilocystidia E Pleurocystidia F Stipitipellis G Tramal Hyphae H Pileipellis. Scale bars: 5.83 μm (A, B, D, E); 3.55 μm (C); 0.12 μm (F–H).


PAKISTAN. Khyber Pakhtunkhwa Province, Swat, Toa, 2800 m a.s.l., on soil under Quercus incana, 15 July 2015, Arooj Naseer & Abdul Nasir Khalid, AST51 (holotype: LAH35245).

Figure 5. 

Phylogenetic relationship of Hygrophorus spp. and its ECM roots from Pakistan and their allied Hygrophorus species based on nrDNA ITS sequences using the Maximum Likelihood method. Sequences generated during this study are in bold letters. Sequences from root tips were labelled as ECM.

Figure 6. 

Molecular phylogenetic analysis of Hygrophorus spp. based on LSU sequences. Maximum likelihood phylogram of Hygrophorus based on nrDNA LSU as generated with RAxML with 1000 bootstrap iterations. Bolded lettering refers to sequences generated in this study.


The species epithet refers to the fine scales on the stipe.

Basidiomata medium sized. Pileus 2.4–2.8 cm, creamy, off-white (7.9GY 6/1) with dark green, greyish fibrils (2.9GY 2.4/2), plano-convex, context moderately thick, margin even, smooth, incurved. Lamellae off-white to beige (4GY 6.8/2.4), subdecurrent to decurrent, thick, spaced to moderately close, L= 41–49, even, entire, undulate at margins. Lamellulae short, in two tiers, 1/3 of length of lamellae. Stipe 2.1–2.4 cm long, 0.3–0.5 cm in diameter, yellowish-green (9.3Y 4.4/2.4) with white (6.9GY 7/1) apex, finely scaled, cylindrical, slightly tapering at base, hollow.

Basidiospores [30/1/1] (4.56–) 4.72–8.1 (–8.76) × (2.5–) 2.8–5.1 (–5.2) μm, avL × avW = 6.5 × 3.84 μm, Q = (1.5–) 1.57 × 1.89 (–1.86), avQ = 1.70, white to light yellow in 5% KOH, ovoid to ellipsoid, smooth, inamyloid. Basidia 30.2–42.3 × 6.8–9.3 μm, hyaline to light green in 5% KOH, narrowly clavate, four-spored, sterigmata long (6.2–7.2 μm), medium thick-walled, densely guttulate. Hymenophoral Trama 3.7–8.2 μm in diameter, bilateral, divergent hyphae, thin-walled, branched, septate. Pileipellis 3–3.7 μm in diameter, an ixotrichoderm, composed of branched septate hyphae. Stipitipellis 3.2–7.0 μm, a thin ixocutis to ixotrichoderm, composed of compact erect hyphae. Clamp Connections present in all tissues.

Habitat and distribution

Solitary on soil under Q. incana, at 2800 m a.s.l., in moist temperate forest of Hindu Kush Himalayan range.


Hygrophorus scabrellus is characterised by a yellowish-green stipe with a white apex that has fine scales on the entire stipe, planoconvex pileus which is off-white with dark green and greyish fibrils.

Hygrophorus scabrellus differs morphologically from the phylogenetically related species H. eburneus. Hygrophorus eburneus has fine scales only at the stipe apex (Table 1), whereas H. scabrellus has scales along the entire length of the stipe. Hygrophorus eburneus has a white stipe (yellowish-green stipe with a white apex in H. scabrellus). Hygrophorus eburneus also differs in having a pure white cap. Our new species H. scabrellus is similar to Hygrophorus cossus (Sow. ex Berk.) Fr. commonly known as Goat Moth Wax Cap, as both share plano-convex pileus. However, H. cossus has greyish white, broader pileus (3–9 cm) and smaller stipe (0.6–2 cm long) (Larsson and Jacobsson 2004) as compared to H. scabrellus that is distinguished by off-white pileus with dark green and greyish fibrils (2.4–2.8 cm) having longer stipe (2.1–2.4 cm). Anatomically, H. cossus has larger basidiospores (7–9 × 4–5 μm) (Larsson and Jacobsson 2004). Molecular phylogenetic analyses based on ITS and LSU sequences also support Hygrophorus scabrellus as a distinct species with strong bootstrap support.


In this paper, two new species of Hygrophorus were studied morphologically and sequences of two DNA regions were analysed for each species. These studies revealed that H. alboflavescens falls into section Pudorini of subgenus Colorati and differs from other species in the section by having yellow dots or patches rather than having entirely white basdiomata. We also confirmed, based on ITS sequences from roots, that this new species forms ECM associations with Q. incana. Hygrophorus scabrellus clusters within section Hygrophorus of subgenus Hygrophorus and differs in colour and stipe scaliness from others in that subgenus. These two new species provide evidence that further research is needed to collect and identify the fungal diversity of Asia, which appears to be a global hotspot of fungal diversity.


  • Bas C, Kuyper ThW, Noordeloos ME, Vellinga EC (1990) Flora Agaricina Neerlandica, Vol. 2. Rotterdam Balkema, 137 pp.
  • Boertmann D (1995) The genus Hygrocybe. Fungi of Northern Europe Vol. I (1st edn). Danish Mycological Society, Greve.
  • Bruns TD (1995) Thoughts on the processes that maintain local species diversity of ectomycorrhizal fungi. Plant and Soil 170: 63–73.
  • Candusso M (1997) Hygrophorus s.l. Fungi Europaei 6. Libreria Basso, Alassio.
  • Fries EM (1874) Hymenomycetes europaei sive Epicriseos systematis mycologici. 755 pp.
  • Hall TA (1999) BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT/7. Nucleic Acids Symposium Series 41: 95–98.
  • Huang HY, Yang SD, Zeng NK, Zhang GL, Hu Y, Tang LP (2018) Hygrophorus parvirussula sp. nov., a new edible mushroom from southwestern China. Phytotaxa 373(2): 139–146.
  • Jacobsson S, Larsson E (2007) Hygrophorus penarioides, a new species identified using morphology and ITS sequence data. Mycotaxon 99: 337–343.
  • Kovalenko A (2012) Knudsen H, Vesterholt J (Eds) In: Knudsen H, Vesterholt J (Eds) Funga Nordica. Agaricoid, boletoid cyphelloid and gasteroid genera. Nordsvamp, Copenhagen, 282–293.
  • Larsson E, Jacobsson S (2004) Controversy over Hygrophorus cossus settled using ITS sequence data from 200 year-old type material. Mycological Research 108: 781–786.
  • Lodge DJ, Padamsee M, Matheny PB, Aime MC, Cantrell SA, Boertmann D, Kovalenko A, Vizzini A, Dentinger B, Kirk P, Ainsworth M, Moncalvo JM, Vilgalys R, Larsson E, Lücking R, Griffith G, Smith M, Norvell LL, Desjardin DE, Redhead SA, Ovrebo CL, Lickey E, Ercole E, Hughes KW, Courtecuisse R, Young A, Binder M, Minnis A, Lindner DL, Ortiz-Sanatan B, Haight J, Læssøe T, Baroni TJ, Geml J, Hattori T (2014) Molecular phylogeny, morphology, pigment chemistry and ecology in Hygrophoraceae (Agaricales). Fungal Diversity 64: 1–99.
  • Miller MA, Pfeiffer W, Schwartz T (2010) Creating the CIPRES Science Gateway for inference of large phylogenetic trees. Proceedings of the Gateway Computing Environments Workshop (GCE), New Orleans, Louisiana, 1–8.
  • Razaq A, Ilyas S, Khalid AN (2014) Taxonomic and phylogenetic affinities of Hygrophorus chrysodon from western Himalayan forests. Austrian Journal of Mycology 23: 21–29.
  • Singer R (1943) Das System der Agaricales. III. Ann Mycologici 41: 1–189.
  • Singer R (1986) Agaricales in modern taxonomy, 4th edn. Koeltz Scientific Books, Koenigstein.
  • Tedersoo L, May TW, Smith ME (2010) Ectomycorrhizal lifestyle in fungi: global diversity, distribution, and evolution of phylogenetic lineages. Mycorrhiza 20: 217–263.
  • Vilgalys R, Hester M (1990) Rapid genetic identification and mapping of enzymatically amplified ribosomal DNA from several Cryptococcus species. Journal of Bacteriology 172: 4238–4246.
  • Werle E, Schneider C, Renner M, Völker M, Fiehn W (1994) Convenient single-step, one tube purification of PCR products for direct sequencing. Nucleic Acids Research 22: 4354–4355.
  • White TJ, Bruns T, Lee SJWT, Taylor JW (1990) Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. PCR protocols: a guide to methods and applications 18(1): 315–322.
  • Young AM (2005) Fungi of Australia: Hygrophoraceae. CSIRO Publishing, Australian Biological Resources Study, Canberra.

Supplementary materials

Supplementary material 1 

Microscopic features of Hygrophorus alboflavescens

Arooj Naseer, Abdul Nasir Khalid, Rosanne Healy, Matthew E. Smith

Data type: media

Explanation note: A–E LAH35243 (holotype). A Pleurocystidia; B Basidaia with Cheilocystidia C, D Basidiopsores; E Pileipellis.

This dataset is made available under the Open Database License ( The Open Database License (ODbL) is a license agreement intended to allow users to freely share, modify, and use this Dataset while maintaining this same freedom for others, provided that the original source and author(s) are credited.
Download file (62.88 kb)
Supplementary material 2 

Microscopic features of Hygrophorus scabrellus

Arooj Naseer, Abdul Nasir Khalid, Rosanne Healy, Matthew E. Smith

Data type: media

Explanation note: A–D LAH35245 (holotype). A Basidiospores; B Hyphal Trama; C Basidiospores; D Pileipellis.

This dataset is made available under the Open Database License ( The Open Database License (ODbL) is a license agreement intended to allow users to freely share, modify, and use this Dataset while maintaining this same freedom for others, provided that the original source and author(s) are credited.
Download file (75.93 kb)