Cantharellus xanthocyaneus Ndolo Ebika & Buyck, 2020
publication ID |
https://doi.org/ 10.5252/cryptogamie-mycologie2020v41a10 |
persistent identifier |
https://treatment.plazi.org/id/03C28781-A351-D305-31C2-6212DF5EFEF6 |
treatment provided by |
Felipe |
scientific name |
Cantharellus xanthocyaneus Ndolo Ebika & Buyck |
status |
sp. nov. |
Cantharellus xanthocyaneus Ndolo Ebika & Buyck , sp. nov.
( Figs 4 View FIG ; 5 View FIG )
MYCOBANK. — MB 835035.
TYPE MATERIAL. — Holotype. Republic of the Congo, Likouala Department ; 3.38 km South from Makao village, Plot 1 in Gilbertiodendron dewevrei forest ( PG1 ); 2°33.84’N, 17°10.12’E; alt. 360 m; 17.XI.2016, S. T. Ndolo Ebika 2353 (holo-, PC [ PC0125128 ]; iso-, HICPC [ HICPC005 ]). GoogleMaps
DIAGNOSIS. — Differs from C. cyanoxanthus essentially in the distinctly smaller, particularly narrower basidiospores, measuring (5.7-)6- 7.0 -8.1(-8.8) × 3.2- 3.7 -4.3 µm, Q = (1.46-)1.56- 1.91 - 2.26(-2.39).
ETYMOLOGY. — Composed of two Greek color terms, xanthos (yellow) and cyanos (dark blue), referring to the dominant colors of the fruiting body.
HABITAT. — On the ground in Gilbertiodendron dewevrei forest, on terra firma.
ADDITIONAL EXAMINED AND SEQUENCED MATERIAL. — Republic Of The Congo, Likouala Department; 3.38 km South from Makao village, Plot 1 in Gilbertiodendron dewevrei forest (PG1); 2°33.84’N, 17°10.12’E; alt. 360 m; 14.XI.2016; S. T. Ndolo Ebika 2333 (para-, PC[PC0125127]; iso-, HICPC[HICPC004]).
DESCRIPTION
Basidiomata ( Fig. 4 View FIG )
Solitary or in pairs, medium-sized and up to 75 mm high.
Pileus ( Fig. 4A View FIG )
Thin-fleshed, 50-63 mm wide, plano-concave to slightly funnel-shaped, mottled with dark purplish-violaceous tinges on a yellowish background, smooth.
Hymenophore ( Fig. 4C View FIG )
Composed of well-differentiated, forking gill folds, pale ochraceous with distinct pinkish tinges, strongly interveined towards the cap margin, up to 7 mm high.
Stipe ( Fig. 4B, D View FIG )
55-57 × 12-17 mm, cylindrical to fluted and bumpy (when fluted), flushed with purple-violaceous to pinkish tones, particularly in its middle portion, distinctly yellowish at the base which is swollen and hollowing, becoming whitish near the junction with the gill folds.
Context
Off-white, rather thin towards the pileus margin.
Smell
Insignificant.
Taste
Unknown.
Spore print
Not obtained.
Spores ( Fig. 5A View FIG )
Ellipsoid to elongated, somewhat concave at the adaxial side and more or less kidney-shaped, (5.7-)6- 7.0 -8.1(-8.8) ×
3.2- 3.7 -4.3 µm {N=58}, Q = (1.46-)1.56- 1.91 -2.26(-2.39), smooth, with a small apiculus.
Basidia ( Fig. 5B View FIG )
46-70 × 5.6- 8 -10 µm {N=9}, predominantly six-spored.
Absent.
Subhymenium
Subfilamentous, composed of narrow, cylindrical cells that are sometimes slightly larger than the basis of the basidia.
Pileipellis ( Fig. 5C View FIG )
Composed of thin-walled, elongated elements, mostly widening towards the septa or towards the tip, quite a few of the terminal and subterminal cells filled with a distinctly dark lilac-brown pigment. Incrusting pigment present on some particularly narrower, subterminal cells and narrow hyphae in the pileipellis.Terminal cells subcylindrical to faintly clavate, mostly 40-100 µm long and (5)8-15(22) µm diam., with thin to slightly thickened (refringent) cell walls.
Clamp connections
Very distinct on hyphae of all tissues.
NOTES
In the field, Cantharellus xanthocyaneus Ndolo Ebika & Buyck , sp. nov., is very similar to C. cyanoxanthus sensu Heinemann because of its color. However, it cannot be the same species because of the distinctly larger basidiospores of C. cyanoxanthus (see below), albeit with a similar length-width ratio. We have measured the holotype of C. xanthocyaneus Ndolo Ebika & Buyck , sp. nov., twice independently (to exclude subjective approaches) with near identical results [S.T. Ndolo Ebika: (5.7-)6- 7.0 -8.1(-8.8) × (3.2-)3.2- 3.7 -4.2(-4.3) µm, Q = (1.46-)1.56- 1.91 -2.26(-2.39) versus Buyck: (6.0)6.4- 6.81 -7.2(7.7) × (3.3)3.4- 3.67 -3.9(4.1) µm, Q = (1.6)1.7- 1.86 -2.0(2.2)]. Also the paratype shows an identical spore size [(5.8)6.3- 6.73 -7.1(7.3) × (2.9)3.3- 3.55 -3.8(4.0) µm, Q = (1.6)1.7- 1.9 -2.0(2.2)].
Heinemann’s (1958) values for spore length of the Central African C. cyanoxanthus seem a bit too low compared to more recent measurements made by Eyssartier (2001) and A. De Kesel (this study) on the holotype (Goossens-Fontana 2082): P. Heinemann (1958: 7.5-9.3 × 4.4-5.4 µm), G. Eyssartier (2001: (7)8- 8.83 -10 × 4- 4.87 -5.5 (6) µm, Q = 1.45- 1.82 -2.0) and A. De Kesel: (7.6-)8.2- 9.4 -10.5 (-10.6) × (4.4-)4.3- 5 -5.6(-5.9) µm, Q = (1.59-)1.61- 1.89 - 2.17(-2.27), but all these are very different from the Malagasy C. littoralis (Buyck & Randrianjohany) Buyck , comb. et stat. nov. (synonym of C. cyanoxanthus sensu Heim ) which has spores that are very similar to those of C. longisporus ( Buyck et al. 2012: (8.1)8.5- 9.01 -9.5(9.8) × (3.5)3.8- 4.07 - 4.4(4.8) µm, Q = (1.9)2.0- 2.21 -2.4(2.5). Some recent collections made near the type locality all confirm the narrower spores of this Malagasy species for a similar length compared to Central African C. cyanoxanthus , resulting in higher Q values [H. 110: 9.08 × 4.15 µm, Q = 2.20; EJ 107: 9.07 × 4.13 µm, Q = 2.21; EJ 108: 8,81 × 4.06 µm, Q = 2.18; EJ 122: 9.06 × 4.08 µm, Q = 2.14].
S |
Department of Botany, Swedish Museum of Natural History |
T |
Tavera, Department of Geology and Geophysics |
PC |
Museum National d'Histoire Naturelle, Paris (MNHN) - Non-vascular Plants and Fungi |
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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