Species of Termitomyces
(Agaricales) Occurring in Achanakmar Biosphere Reserve, Chhattisgarh
Srishti Verma1,
Mahesh Tiwari2, R.V. Shukla3, Kamlesh Shukla1*
1
*School of Studies in Biotechnology, Pt.
Ravi Shankar Shukla University, Raipur (C.G.)
2,
3 Department of Botany C. M. D. College
Bilaspur (C.G.)
Abstract:
The
Agarics as a group, occurs in a varieties of habitat. Some species exist in
areas that are geographically separated, while some are known only from
restricted areas and many species do seem to show preference for a certain type
of natural habitats as well as for a particular substrate. An extensive exploration
of wild mushrooms carried out from 2019 to 2021 at different forest ranges of
Achanakmar Biosphere Reserve,Chhattisgarh India. Seven different species of Termitomyces
namely Termitomycesclypeatus, T.
microcarpus, T. rabuorii, T. streatus, T. radicatus, Termitomyces sp. -1,
Termitomyces sp -2, were found in edible
form. So far members of the group which are found in soil, dung, plant
derbies, independently or in association with particular plant species has
minimal documentation and germ-plasm collection from Chhattisgarh state, which
is known for the largest forest land and the tribal population.
Key Words: Agarics, Chhattisgarh, Diversity,
Termites, Termitomyces.
1.
Introduction
Recent studies have
diversified the existence of Termitomyces species in Tanzania,
Uganda, of Africa and South - east and west India. The species of Termitomyces grow
in association with termites were found to originate from tropical forests (Mosseboet
al., 2017; Nobre and Aanen, 2010) like ancient Sal forests of Central – India. The genus is absolutely
dependent on the possible symbiont relative termites. The number of
fungus-farming Termites’ species is reported approximately 165 in Africa, that
belong to 11 genera (Kambhampati and Eggleton,
2000), which are underestimated considering on the
novel termite species that has beenalready discovered (Makonde et al., 2013).There are about more than 30 Terimitomyces
species have been globally recorded (Tang et al., 2020; Sathiya et al., 2020).
The
Achanakmar Biosphere Reserve (ABR) accounts for the occurrence
and distribution of many unexplored novel varieties of Termitomyces and Termites due to the
richness of variety of tree species. Because the large tree canopies and huge
amount of litter fall in ground surface provide suitable home to various
species of both the biological agents. The Sal tree provides shelter for many
more species of Termites to build their nests between ridges and furrow at
various heights of tree trunks. Nevertheless, the Sal and many other native tree
species return back substantial amount of leaf litter that protects soil by water run-off conserving soil moisture
under which Termites and microorganisms feed upon and regulate the process
of biodegradation, decomposition to humification.
In fact, the species of Termitomyces arelinked with the economic
importance of the termites as not a single species of Ternitomyces could be grown
independently (Kuja et al., 2014) so far.This is an indication of mutualistic
relationship of Termitomyces species with an animal group to place the
genus in advance position rather than primitive ectomycorrhizal group. Since
the symbiosis phenomenon denoting primitive features of the forest which is a powerful ecological capital in tropics maintaining natural
phenomenon (Temperature, precipitation, etc.) to sustain biological lives.
However, the inner dynamics of these forests is fragile as everything in the
ecosystem is so interdependent that upsetting one part can lead to unknown
damage or even destruction of the whole.
Presently,
Termitomyces is one of the most
popular wild mushrooms among the tribals, because it valued as food supplements
and in therapeutic purposes for treatment of various diseases (Fui et al., 2018; Hsieh et al., 2018). The tribals
store these mushrooms for off season uses by preserving them traditionally by
sun drying and smoking process. The Termitomyces heimii is one of the
most popular wild mushrooms, which is under immense collection pressure in the
state. Since Chhattisgarh state is the largest tribal state in the country and
known for the richness of sal forests, where many of unexplored novel varieties of mushroom
are expected, therefore presentstudy brought to light, numerous lesser known Termitomyces species of the ABR. The study
on occurrence and distribution of gilled fungi has been conducted with the help
of baiga tribes who are well acquainted with the periods of occurrence in
varieties of habitat.
2.
Material and Methods
Mushrooms
were collected in the morning hours and the essential study of the collected
specimens was done at the spot itself, which includes the recording of
necessary general information and morphological characteristics regarding the
specimen. Habitat photographs of the mushrooms were also taken. The
preservation of the specimens was done by drying the specimens in the specially
designed cabinet over hot air convector.
The
completely dried specimens were packed in (6” x 4”) sized polythene bags
containing crystalline silica gel to moisture absorber and naphthalene balls to
prevent the insect-pest infestation. The packets containing the dried samples
were then labeled in brief. The spore prints were obtained by removing the
pileus and placing over white paper with gills facing the paper and covered
with a large petri dish. After preservation of all samples, microscopic
observation was done for the identification of particular mushroom.
2.1. Key to the species of Termitomyces:
1.
Carpophores small to medium sized; veil
absent ……………………..………… 2
1.
Carpophores medium sized; veil present
………………………………………... 6
2.
Pileus less than 4 cm diam.;
pleurocystidia inconstant ……………………...…... 3
2.
Pileus more than 4 cm diam.;
pleurocystidia always present …………………..... 4
3.
Pileus 0.6 – 1.2 cm diam., surface
yellowish white with mahogany brown, umbo perforatorium; spore 4.25 – 7 × 2.5 –
5 µm; pseudorrhiza and pleurocystidia absent…………………………………………….…………………….… T
.microcarpus
3.
Pileus 3.9 cm diameter,
surface orange grey with dark brown, conical broad perforatorium; spore 6.5 –
9.75 ×
4.25 – 6.5 µm; pseudorrhiza and pleurocystidia present
………………………………………………………………………………….. T. sp. 1
4.
Pseudorrhiza more than 6.2 cm long; gill
edges sterile, cheilocystidia without pedicellate cells; pileus plano-convex to
applanate with acute to spiniform perforatorium, surface orange grey, brownish orange to yellowish grey ……………….….……………T.striatus
5.
Pileus 5.6 – 7 cm,
plano-convex with dark, spiniform perforatorium, surface brownish orange to
yellowish grey; pseudorrhiza greyish white to yellowish grey, spore 5.5 – 9.25 × 4 – 5 µm
……………..……………………………………………….….. T. clypeatus
5.
Pileus 5.2 - 6.6 cm, applanate with fawn
brown, acute perforatorium, surface orange grey; pseudorrhiza dark brown,
crusty; spore 6.25 -8.25 × 3.25 – 5µm…………………………………………………………………..…………T.
rabuorii
6.
Pileus 6 – 9.2 cm broad,
surface shiny white with greyish brown to brownish orange, broad umbo perforatorium;
pseudorrhiza 30 cm long, smooth; annulus double, spore deposit pinkish white,
spores 6.5 – 10.25 × 4.5 – 6.25µm
………….…………. T. sp. 2
7.
Pileus grayish brown or pale orange,
smooth, with dark spiniform umbo, Pseudorrhiza
present; cystidia absent……………………………………….T.radicatus
3.
Result and Discussion
Termitomyces
Arch. Mus. Nat. Hist. Nat. Ser. 6(18): 147 (1942)
Most of the
species of Termitomyces are highly
valued edible mushroom. The taxonomy of the genus has been well studied by
Singer (1986). He reported 13 species from all over the world. Manjula (1983)
listed 10 Indian species of Termitomyces.
Karunet al., (2013)
listed 5 species of Termitomyces. The fungus represents the Indian
mycoflora growing frequently throughout the country and studied by many Indian
workers including Sharma et al., (2017); Lakhanpal (2014);Raman et al., (2018);
Patil et al., (1979); Singh (1965); Sharma et al., (1977);Bhavaniet al.,
(1980).
Generic characteristics: Habit of the
carpophores pluteoid, usually fleshy and large, with prominent, often sharply
differentiated umbo; stipe central; spore print pink, lamellae free to adnexed
but with decurrent tooth, stipe with a pseudorrhiza and with simple or double
veil epicutis consisting of filamentous, hyaline hyphae, hymenophoral trama
bilateral, thin, filamentous hyphae, spores hyaline, inamyloid, with a hilum of
the open pore type, ellipsoidal, smooth. Basidia normal, cystidia present,
tramal hyphae inamyloid, without clamp connections tramal system monomitic.
Eight
different species namely T. clypeatus, T.
microcarpus, T. rabuorii, T. streatus, T. radiatus, Termitomyces sp. -1,
Termitomyces sp -2, belonging to Termitomyces
genera were identified based on the key identification features described
by Pegler and Vanhaecke (1994).
Termitomyces clypeatus Heim, Bull. Jard. Bot. Etat.21: 207, 1951.
(Figure 1)
Carpophores 18 – 20.4 cm
in height including pseudorrhiza. Pileus 5.6 – 7 cm broad, first conical to
convex, then expanding to plano-convex with dark, spiniform perforatorium,
surface brownish orange to yellowish grey (6C4 – 4B2), viscid when moist then
dry, smooth, glabrous, margin irregular, lobed, splitting at maturity, plane to
plano- decurved; cuticle fully peeling; flesh 0.3 cm in thickness, narrowing
down to the margin, white to light cream, fleshy, unchanging; taste mild, odour
fruity. Lamellae free, crowded, unequal, 0.5 cm wide, lamellulae 2-3 sized,
orange white (5A2), unchanging, edges serrate, normal. Spore deposit light
orange (5A4) Stipe 7.5 – 8.2 cm above the ground, 0.6 - 0.8 cm near the pileus,
0.9 – 1.1 cm broad near the soil level, central, cylindrical, fleshy, solid,
upper portion of the stipe fibrillose, elsewhere smooth, greyish white to
yellowish grey (4B1 – 4B2); pseudorrhiza 10.2 – 13 cm, expanded up to 1.6 cm
broad then narrowing down (0.6 cm diameter); annulus absent.
Spore 5.5 – 9.25 × 4 – 5 µm, ellipsoid, thin walled,
hyaline, with few guttule contents, inamyloid. Basidia 21.5 – 24.75 × 7.25 – 8
µm in size, clavate to narrowly clavate, thin walled, 4-sterigmata, sterigmata
up to2.5 µm long. Gill edges sterile; cheilocystidia few, 22.5 – 42.5 × 13.5 -
25 µm, pyriform, thin walled, hyaline.Pleurocystidia 25 – 85 × 15.5 – 37 µm,
scattered, pyriform to broadly clavate, thin walled.
Pileus cuticle made up of radially
arranged, septate, branched, thin walled, repent hyphae measuring 3 – 7.75 µm
diameter. Pileus context homoiomerous, made up of branched, septate, interwoven
hyphae measuring 2.5 – 12.5 µm diameter, inflated up to 27.75 µm diameter,
oleiferous hyphae present. Hymenophoral trama regular to slightly bilateral
divergent, formed of septate, branched, thin walled hyphae measuring 5.75 –
14.75 µm diameter, inflated up to 22.5 µm diameter; subhymenium
pseudoparenchymatous, 11.5 µm wide.Stipe hyphae septate, branched, arranged
parallel, thickened wall, measuring 3.5 – 12.25 µm diameter, inflated up to
24.75 µm diameter. All hyphae lacking clamp connections.
Fig. 1 Teritomyces clypeatus A.
Basidiocarps, B. Basidiospores, C. Basidia, D. Cheilocystidia, E.
Pleurocystidia, F. Fruiting body; Scale bars A=2cm, B-E=10µm.
Collection examined: Chhattisgarh: Achanakmar Biosphere Reserve (ABR), Tilai
dabra (660 M), growing gregariously to scattered on humicolous soil under Madhuca indicaand Terminalia chebulatrees.
Comments:Diagnostic
features of the above examined collection are in close agreement with T. clypeatus as described by Pegler
(1977) except that the spores and pleurocystidia are larger in size and gill
edges are serrate rather than entire. This specimen also seems close to North
Indian collection as reported by Atri et al., (2005). This species has been
earlier reported from Shillong by Verma(vide: Pegler and Vanhaecke, 1994) and
Patiala (Punjab) by Atri et al., (2005).
Termitomyces microcarpus (Berk. & Br.) Heim, Mem. Acad. Sci. Instit. France 64: 72, 1941.
(Figure 2)
Carpophores 1.4 – 3.2 cm in height.
Pileus 0.6 – 1.2 cm diameter, convex, expanding with umbonate centre, surface
yellowish white (1A2), dry, glabrous, radially streaked, centre mahogany brown
(8E7), margin decurved, entire, irregular, splitting with age; cuticle fully
peeling; flesh less than 0.1 cm, white to yellowish white, unchanging; taste
and odour mild . Lamellae adnexed, subdistant to close, unequal, 0.1 cm wide,
whitish cream in colour, lamellulae present, unchanging, gill edge serrate.
Spore deposit greyish orange (5B3), Stipe 1 – 2.9 cm in length, 0.1 - 0.2 cm
diameter, central, cylindrical, equal with slightly bulbous base, white when
young then yellowish white (1A2) with maturity, smooth, hollow, pseudorrhiza
absent, annulus absent.
Spore 4.25 – 7 × 2.5 – 5 µm, ovoid
to ellipsoid, smooth, thin walled, inamyloid, with guttulate contents. Basidia
19.7 – 25 × 7 – 7.7 µm, clavate, guttulate, 2–4 spored, sterigmata up to 2.75
µm long. Gill edges heteromorphous; cheilocystidia 18 – 32.5 × 7.7 – 18.5 µm,
pyriform to clavate, mostly clavate, slightly thickened wall. Pleurocystidia
not recovered.
Fig. 2 Termitomyces
microcarpus (Berk. & Br.) Heim, A. Basidiocarps, B. Basidiospores, C.
Basidia, D. Cheilocystidia, E. Fruiting body; Scale bars A=2cm, B-D=10µm.
Pileus cuticle formed of slightly
interwoven, septate, slightly thickened wall hyphae measuring 2.5 – 10 µm in
diameter. Pileus context made up of interwoven, septate, thin walled hyphae
measuring 2.75 – 12 µm in diameter. Gill trama regular to subregular, made up
of 4.5 – 10.25 µm diameter, septate, branched hyphae; subhymenium
pseudoparenchymatous. Stipe hyphae formed of septate, branched, thickened wall
hyphae measuring 2 – 7.5 µm in diameter, inflated up to 22.5 µm, oleiferous
hyphae present. All hyphae lacking clamp connections.
Collection examined: Chhattisgarh: Achanakmar Biosphere Reserve (ABR),
Bharosang - Atariya (520 M), growing in cluster on sandy soil under Shorea robusta tree.
Comments: The
details of the present specimen are agreement with T. microcarpus as described byPegler (1977) but slightly differ in
the size of the spores (4.25 – 7 × 2.5 – 5 µm) and basidia (19.7 – 25 × 7 – 7.7
µm). Pleurocystidia could not be recovered in the present species which are
reported (Pegler, 1977) to be inconstant and rare. It is characterised by small
sized carpophores, yellowish white pileus with brownish umbo and absence of
pseudorrhiza and veil. This species was recorded earlier from India by
Natarajan (1977a) from Tamil Nadu, Rawla et al., (1983) from Chandigarh
(Punjab) and Atri et al., (1995) from Patiala (Punjab). Here it is a first record from Chhattisgarh.
Termitomyces rabuorii Otieno. Proc. E. Afr. Acad, 21:
115,t.3 bis., 1966.
(Figure 3)
Carpophores up to 14.8 cm in height
including pseudorrhiza. Pileus 5.2 - 6.6 cm broad, convex then expanding and
becoming applanate with acute perforatorium, surface orange grey (5B2), centre
fawn brown (7E4), smooth, glabrous, brown hair like lines running on the
surface, margin decurved, splitting at maturity, lobed, crenate to eroded;
cuticle fully peeling; flesh 0.3 cm at disc, narrowing down to margin, white,
unchanging on cutting or bruising, fleshy; taste and odour mild. Lamellae free,
crowded, 3 -4 sized, 0.3- 0.4 cm wide, white to creamish, unchanging, fragile,
edge serrate. Spore deposit pale orange (5A3). Stipe 8.1 cm in length, 0.6 cm
in diameter at apex, 0.8 – 1 cm broad near the soil level, white to creamish
white, shiny, fleshy-fibrous, solid, fibrillose, unchanging on cutting or
bruising, pseudorrhiza up to 6.2 cm long, dark brown, crusty, annulus absent.
Spore 6.25 -8.25 × 3.25 – 5 µm,
ovoid to ellipsoid, thin walled, having one or more guttulate contents, with
some angular spores, inamyloid, hyaline. Basidia 21.5 – 23.25 × 6 – 7µm,
clavate, guttulate, thin walled 4 spored, sterigmata up to 3.25 µm long. Gill
edges sterile; cheilocystidia 18.25 -30 × 10 – 17.5 µm, pyriform, hyaline, thin
walled. Pleurocystidia 28.75 – 42.5 ×15 – 24.5 µm, broadly clavate to pyriform,
hyaline thin walled.
Pileus epicutis made up of radially
arranged, branched, septate, repent hyphae measuring 2.5 – 5.25 µm. Pileus
context formed of branched, septate, almost parallel hyphae measuring 2.5 -19.5
µm diameter, slightly thickened wall, some hyphae retain the stain. Gill trama
subregular to slightly bilateral, hyphae measuring 4 – 14.75 µm, septate;
subhymenium pseudoparenchymatous, 7.5 – 9 µm wide. Stipe hyphae septate
branched, parallel, measuring 2.25 – 23 µm in diameter. All hyphae lacking
clamp connections.
Fig. 3 Teritomyces
rabuorii Otieno, A. Basidiocarps, B. Basidiospores, C. Basidia, D.
Cheilocystidia, E. Pleurocystidia, F. Fruiting body; Scale bars A=2cm,
B-E=10µm.
Collection examined: Chhattisgarh: Achanakmar Biosphere Reserve (ABR),
Tilaidabra (660 M), growing solitary to gregarious near and on termitaria under
Dendrocalamus
strictus tree.
Comments: The
present specimen resemble with T.
rabuorii in their macroscopic and microscopic details. T. rabuorii has been reported by Natarajan (1977b) from Madras and
Atri et al., (2005) from Patiala (Punjab). This collection confirms well with T. rabuorii as reported by Atri et al.,
(2005) except that the basidia (21.5 – 23.25 × 6 – 7µm instead of 22.5 – 30 ×
7.5 - 9 µm) and cheilocystidia (18.25 -30 × 10 – 17.5 µm instead of 24 – 42 ×
10.5 – 21 µm) are smaller in size.
Termitomyces striatus(Beeli) Heim var. annulatus
Heim. Mem. Acad. Sci. Instit. France 64: 47, 1941.
(Figure 4)
Carpophores up to 34.7
cm in height includingpseudorrhiza. Pileus 6 – 9.2 cm broad, conical at first
then convex to parabolic and finally applanate with broad umbo perforatorium,
surface shiny white (2A1), centre greyish brown to brownish orange (9D3 – 6C3),
viscid when moist, glabrous, having fine squamulose, innate, margin, regular,
plane to decurved, splitting at maturity, crenate; cuticle fully peeling; flesh
up to 0.7 cm in thickness, white, fleshy, unchanging on cutting or bruising;
taste fruity, odour mild. Lamellae free, crowded, 4-5 length, unequal, 0.5 -
0.6 cm in width, white (4A1), edges serrate, unchanging. Spore deposit pinkish
white (8A2).Stipe 3 cm above the ground, 1.1 – 2.6 cm broad, broader near
annulus, central, cylindrical, fleshy-fibrous, solid, fibrillose, white, pseudorrhiza
30 cm long, 0.6 - 0.8 cm in diameter, orange grey (5B2), almost smooth,
somewhere appressed squamulose to cuticle layer; annulus double, membranous,
superior, persistent.
Spore 6.5 – 10.25 × 4.5 – 6.25 µm, spherico-ellipsoid
to broadly ellipsoid, smooth, thin walled, guttulate, inamyloid. Basidia 27.25
– 37.25 × 7.5 – 8.75 µm, clavate, with guttulate contents, 4-spored, sterigmata
up to 3.25 µm long. Gill edges serrate; cheilocystidia 29.75 – 92.5 × 9.75 –
34.75 µm in size, pyriform to clavate, some with pedicellate cells, slightly
thickened wall. Pleurocystidia 25.5 – 52.25 × 9.75 – 31.5 µm, pyriform to
broadly clavate, thin walled.
Pileus cuticle epicutis formed of
septate, branched, slightly interwoven, dense, thin walled hyphae measuring 1.5
– 3.75 µm diameter, sometimes gelatinized. Pileus context made up of septate,
branched, interwoven hyphae measuring 2.75 – 9.75 µm diameter, inflated up to
21.25 µm diameter, oleiferous hyphae present. Hymenophoral trama regular to
slightly bilateral divergent, formed of septate, branched, thin walled hyphae
measuring 2.25 – 15 µm in diameter; subhymenium made up of subregular to
interwoven hyphae measuring 4.75 – 9.25 µm. Stipe hyphae septate, branched,
arranged almost parallel, measuring 2.25 – 11 µm in diameter, inflated up to 25
µm diameter, oleiferous hyphae present. All hyphae lacking clamp connections.
Fig. 4 Teritomyces striatus (Beeli)
Hei var. annulatus Heim, A. Basidiocarps, B. Basidiospores, C. Basidia,
D. Cheilocystidia, E. Pleurocystidia, F. Fruiting body; Scale bars A=2cm,
B-E=10µm.
Collection examined: Chhattisgarh: Achanakmar Biosphere Reserve (ABR),
Bharosang - Atariya (520 M), growing gregariously on humicolous soil near
termitaria under Shorea robusta tree.
Comments: Diagnostic features of the above examined collection are in
close agreement with Termitomycesstriatus var.
annulatusas described by Atri
et al., (2005) and Pegler (1977) except that
the spore, basidia and cheilocystidia are
larger in size. The main characteristics of this
specimenare medium to large size carpophore, shiny white pileus with greyish
brown, broad umbo centre, double annulus and long pseudorrhiza with cuticle
layer on the surface. Termitomycesstriatus
var. annulatus has been
earlier reported from Patiala (Punjab) by Atri et al., (2005).
Termitomyces radicatus Natarajan Curr. Sci. 46: 679-680
(1977)
(Figure 5)
Pileus : upto 5cm in diameter, convex with umbonate perforatorium, dark
brown or grey umbo than the rest of the pileus, smooth, slightly viscid, margin
serrulate with white flesh; Gills : free, white, soft, edges entire, close to
crowded; Stipe : cylindrical solid,
tapering towards base with short pseudorrhiza below soil line, white; Annulus :
single layered, papery, thin, superior broad, white.Basidiospores : 6-8 × 4-6µm, elliptical to
cylindrical, non-amyloid, hyaline, smooth; Basidia : 20-28 × 6-8µm, clavate, 4-spored, hyaline, cystidia not observed;
Pileus cuticle : composed of septate
irregularly arranged, hyaline, interwoven hyphae; Hymenophoral trama: regular, hyphae, parallely arranged,
septate, hyaline; Stipe cuticle :
made up of parallely arranged septate, hyaline hyphae.
Habit, Habitat & Distribution: Terrestrial, solitary, found
growing on termite nests and in open lawns during rainy season. The species was
found distributed along the forest ranges of Motinala of Mandla district.
Locally not consumed by tribals.
Fig.5 Termitomyces
radicatus, A. Basidiocarps, B. Basidiospores, C. Basidia, D. Fruiting body;
Scale bars A=1cm, B-C=10µm.
Collection studied: Motinala (Mandla), 18th July 1998 (FGCCM 290).
The species has been reported from J&K by Natrajan (1977). The macroscopic and microscopic
details of the present specimen resembles well with T. radicatus as described by Natrajan (1977) except slight difference in umbo colour. Since
there is not report of its occurrence from MP, it constitutes a new addition to
mushroom flora of MP.
Termitomyces Heim Arch. Mus. Nat. Hist.
Nat. VI, 18: 148 (1942).
Termitomyces sp. 1
(Figure 6)
Carpophores up to 15.1
cm in height. Pileus 8.4 cm broad, convex then expanding to almost flat with
acute, cinnamon brown (6D6) perforatorium, surface white to greyish white (4A1
– 4B2), viscid when moist, glabrous, white lines running from centre to margin,
margin irregular, fine splitting, plane, entire; cuticle fully peeling; flesh 0.4 - 0.5 cm
thick, narrowing down to the margin, white, fleshy, unchanging; taste mild,
odour sweet. Lamellae free to adnexed, crowded, unequal, 4-5 length, 0.4 cm
wide, normal, white then yellowish grey (4B2), unchanging, edges serrate. Spore
deposit yellowish grey (4B2). Stipe 10.3 cm long above the ground, 1 cm
diameter, central, upper portion flattened, base cylindrical, solid, fleshy, striate, white (1A1), shiny,
unchanging, expanded to 1.9 cm near the soil level then narrowing down to
form pseudorrhiza measuring 4.2 cm in
length; pseudorrhiza solid, fleshy, crusty, cognac brown (6E7); annulus single,
ring like, membranous.
Spore 6.75 – 8.75 × 4.5 – 5.5 µm, ovoid to slightly
ellipsoid, thin walled, hyaline, containing one to few guttules, inamyloid.
Basidia 20.75 - 25 × 6 – 7.75 µm in size, clavate to narrowly clavate, thin
walled, 4-spored, sterigmata up to 2 – 2.6 µm long. Gill edges sterile;
cheilocystidia abundant, 36 – 63.5 × 20.5 – 27.25 µm, pyriform to inflated clavate,
thin walled, hyaline, pedicellate. Pleurocystidia 28 – 72.25 × 17.5 – 36.25 µm
in size, scattered, inflated clavate to pyriform, thin walled, hyaline.
Pileus cuticle an epicutis made up
of radially arranged repent, septate, thin walled hyphae measuring 2.25 – 5.25
µm in diameter. Pileus context formed of branched septate, interwoven, thin
walled hyphae measuring 4 – 15 µm diameter, mostly inflated, inflated up to 50
µm diameter. Hymenophoral trama regular to subregular, made up of septate,
branched, thin walled hyphae measuring 4.25 – 12.5 µm diameter, olieferous
hyphae present, rare; subhymenium pseudoparenchymatous to interwoven, 8 –
12.5µmwide. Stipe hyphae septate, branched, somewhat parallel, measuring 2.25 –
9.5 µm in diameter inflated up to 24 µm diameter.All hyphae lacking clamp
connections.
Fig. 6 Teritomyces
sp. 1, A. Basidiocarps, B. Basidiospores, C. Basidia, D. Cheilocystidia, E.
Pleurocystidia, F. Fruiting body; Scale bars A=2cm, B-E=10µm.
Collection examined: Chhattisgarh: Achanakmar Biosphere Reserve (ABR), Lamni
(565 M), growing solitary near termitaria on humicolous soil under Peltophorum ferrugineum tree.
Comments: This
specimen is a species of genus Termitomyces,
characterised by white to greyish white pileus
with cinnamon brown, obtusely rounded perforatorium, presence of dark, crusty
pseudorrhiza and single, ring like, membranous annulus. This specimen seems
close to description given for Termitomyces
eurrhizus by Pegler (1977). However it differs in some morphological and
microscopical characters including smaller carpophores, short pseudorrhiza,
spore print colour, and larger cheilocystidia and pleurocystidia. The present
specimen may be a variant of T. eurrhizus
as the variability of this species has been reported by Pegler (1977). To
confirm this species to species level,expert consultation is being made.
Termitomyces Heim Arch. Mus. Nat. Hist.
Nat. VI, 18: 148 (1942).
Termitomyces sp. 2
(Figure 7)
Carpophores up to 6.3 cm
in hight. Pileus 8 cm broad, convex then plane finally slightly uplifted with
broad umbo, surface white to greyish white (2A1 – 4B1), centre violet brown
(10F6), smooth, dry, glabrous, margin plane to slightly uplifted, splitting at
maturity, edges crisped; cuticle fully peeling; flesh 0.4 cm in thickness,
narrowing down to the margin, white, unchanging, fleshy; taste mild, odour
fragrant. Lamellae free, crowded, unequal, lamellulae 3 sized, moderately
broad, 0.3 cm wide, greyish white (4B1), unchanging, fragile, edges
serrate.Spore deposit creamish white. Stipe up to 3.2 cm above the ground, 1 cm
broad, central, cylindrical, expanded to 1.5 cm near the soil level, solid,
smooth to slightly striated, fleshy, white to whitish cream; pseudorrhiza 2.5
cm long, up to 0.7 cm in diameter, crusty, solid to stuffed; annulus absent.
Spore 5.5 – 7.5 × 4.5 – 5 µm, ovoid to ellipsoid,
creamish, smooth, hyaline, guttulate, inamyloid. Basidia 20 – 27.5 × 7.5 – 9.25
µm in size, clavate, hyaline, 4-spored, sterigmata up to 1.5 µm long. Gill
edges heteromorphous with crowded cheilocystidia; cheilocystidia 31 – 37 × 12.5
– 20.5 µm, abundant, hyaline, pyriform, clavate to ventricose, some with 1-2
short pedicellate cells. Pleurocystidia 32.5 – 34 × 12.5 – 13.75 µm, few,
clavate, slightly thickened wall.
Pileus cuticle an epicutis, made up
of radially parallel, septate, thin walled hyphae measuring 2 – 4.25 µm in
diameter, inflated up to 7.75 µm diameter. Pileus context homoiomerous, formed
of septate, branched, interwoven, thin walled hyphae measuring 3.75 – 12 µm
diameter, inflated up to 35 µm in diameter. Hymenophoral trama regular, made up
of septate, branched, parallel, thin walled hyphae measuring 3.75 – 11.5 µm
diameter; subhymenium 2-3 layered, pseudoparenchymatous. Stipe hyphae septate,
branched, hyaline, thickened wall, measuring 5 – 10 µm in width, inflated up to
27.5 µm diameter. All hyphae lacking clamp connections.
Fig. 7 Teritomyces
striatus sp. 2, A. Basidiocarps, B. Basidiospores, C. Basidia, D.
Cheilocystidia, E. Pleurocystidia, F. Fruiting body; Scale bars A=2cm,
B-E=10µm.
Collection examined: Chhattisgarh: Achanakmar Biosphere Reserve (ABR), Atariya
(543 M), growing solitary on humicolous soil near termitaria under Terminaliatomentosatree.
Comments: The
medium sized carpophores, plane to slightly uplifted pileus with broad umbo,
absence of annulus, stipe which is broader at the soil level and short, crusty
pseudorrhiza are the main characters of this specimen. The morphological and microscopic details of this specimen
show full conformity with the genus Termitomyces.
This is one of the most complicated specimens in
our collections of genus Termitomyces
which shows some considerable difference from earlier reported species. It’s
may be a new variety or new species of the genus Termitomyces.
4.
Conclusion
Species of Termitomyces are one
of the wild mushrooms, which have been reported to be under immense collection
pressure in the forest areas of chhattisgarh. These are collected and sold in
the market during the rainy season when other minor forest products are not
available.
The ancient Sal tree known for mycorrhizal
association with mushrooms providing shelter to insect, reptiles, mammals
including tribals, has a sad history for felling down and planting other types
of tree species (Teak, Pine etc.) in its own habitat. This has played
devastating role to cut down not only symbiotic association with Termites and Termitomyces, but other wild mushrooms
which prefer to grow only in rhizomorphic network of the Sal tree.
Surprisingly, we have not been brought it for consideration that above part of
upsetting may lead to unknown damage or even destruction of the whole forest
ecosystem.So far due to unfavorable conditions many wild macro fungi species
have reached up-to the verge of extinction and no effort has been made for
consideration of the mushroom flora valued for human health and nutrition.
Therefore, documentation and conservation activities in favour of wild
mushrooms and their associates should be taken up at the priority basis within
the corresponding states in central part of the country.
References
Atri, N. S., Kaur, A., & Kour, H. (2005). Systematics and
Sociobiology of Termitophilous mushrooms from Punjab. The fungi-diversity
and conservation in India, 159-182.
Atri, N. S., Saini, S. S., & Kaur, G. (1995). Studies on north
Indian Agarics: The Genus Termitomyces.
Mushroom Research, 4:7-10.
Bhavani
Devi, Nair, M. C. and Menon, M. R. (1980). Termitomyces
robustus: an addition to Indian edible mushrooms. Kavaka,8: 53-54
Fui, F. S., Saikim, F. H., Kulip, J., & Seelan, J. S. S. (2018).
Distribution and ethnomycological knowledge of wild edible mushrooms in Sabah
(Northern Borneo), Malaysia. Journal of Tropical Biology & Conservation
(JTBC), 203â-222.
Heim,
R. (1942). Les Champignons des termitieres Revue
Scientifique, 80: 69-86.
Hsieh, H. M., & Ju, Y. M. (2018). Medicinal components in Termitomyces mushrooms. Applied
Microbiology and Biotechnology, 102: 4987-4994.
Kambhampati S, Eggleton P. (2000). Taxonomy and phylogeny of
termites. In: Abe T, Bignell DE, Higashi M. ed. Termites: Evolution, Sociality,
Symbioses Ecology. Kluwer Academic Publishers, Dordrecht, 1-23.
Karun, N. C., & Sridhar, K. R. (2013). Occurrence and distribution
of Termitomyces (Basidiomycota,
Agaricales) in the Western Ghats and on the west coast of India. Czech
Mycology, 65(2), 233-254.
Kuja, J. O., Boga, H. I., Matiru, V., & Makonde, H. M. (2014).
Diversity, properties and ecological significance of the genus Termitomyces
associated with fungus farming termites in Africa. Internat J Micro Mycol, 2: 29-36.
Lakhanpal, T. N. (2014). Mushroom biodiversity in India: prospects and
potential. In Proceedings of the 8th international conference on mushroom
biology and mushroom products (ICMBMP8) (pp. 7-16).
Makonde, H. M., Boga, H. I., Osiemo, Z., Mwirichia,
R., Stielow, J. B., Göker, M., & Klenk, H. P. (2013). Diversity of
Termitomyces associated with fungus-farming termites assessed by cultural and
culture-independent methods. PloS one, 8(2), e56464.
Manjula, B.
(1983). A revised list of the agaricoid and boletoid basidiomycetes from India
and Nepal. In:Proceedings/Indian Academy
of Sciences. Vol. 92, No. 2, pp. 81-213. Springer India.
Mossebo, D. C., Essouman, E. P. F., Machouart, M. C., & Gueidan, C.
(2017). Phylogenetic relationships, taxonomic revision and new taxa of Termitomyces (Lyophyllaceae,
Basidiomycota) inferred from combined nLSU-and mtSSU-rDNA sequences. Phytotaxa,
321:
71-102.
Natarajan, K. (1977) b. South Indian
Agaricales-III. Kavaka,5: 35-39.
Natarajan, K. (19770) a. South
Indian Agaricales-II. Mycologia,. 69: 185-189.
Nobre T, Aanen DK. (2010). Dispersion and colonization by
fungus-growing termites; vertical transmission help, but then? Landes Bioscience,3: 248-250.
Patil, S. D.,
Nair, L. N. & Kapadnis, B. T. (1979). Studies on fleshy fungi of Western
India I. Genus Termitomyces J. Univ. Poona.,
Sci. and Technol,52: 349-354
Pegler, D. N. (1977) A preliminary agaric
flora of East Africa. Kew Bull. Additional
series VI Royal Botanic gardens Kew.
Pegler, D. N. and Vanhaecke, M.
(1994). Termitomyces of Southeast
Asia. Kew Bull.,49: 717-735.
Raman, J., Lee, S. K., Im, J. H., Oh, M. J., Oh, Y. L., & Jang, K.
Y. (2018). Current prospects of mushroom production and industrial growth in
India. Journal of Mushroom, 16: 239-249.
Rawla, G. S., Arya, S. and Sarwal,
B. M. (1983). Species of Termitomyces Heim
from Chandigarh India. Bibliotheca
Mycologia,91: 13-21.
Sathiya Seelan, J. S., Shu Yee, C., She Fui, F., Dawood, M., Tan, Y. S.,
Kim, M. J., & Lim, Y. W. (2020). New Species of Termitomyces (Lyophyllaceae, Basidiomycota) from Sabah (Northern
Borneo), Malaysia. Mycobiology, 48: 95-103.
Sharma, A. D.,
Jandaik, C. L. & Munjal, R. L. (1977). Some fleshy fungi from Himachal
Pradesh. Ind. J. Mush.,3: 12-15.
Sharma, V. P., Annepu, S. K., Gautam, Y., Singh, M., & Kamal, S.
(2017). Status of mushroom production in India. Mushroom research, 26:
111-120.
Singer, R. (1986).
The Agaricales in Modern Taxonomy, 4th edn, Seven Koeltz Scientific
Books, Koenigstein, Germany.
Singh, S. (1965) Termitomyces albuminosus (Berk.) Heim.
On active mounds of Odontotremes obesus (Rambur)
Holmgren. J. T. D. A. 11(4).
Tang, S. M., He, M. Q., Raspe, O., Luo, X., Zhang, X. L., Li, Y. J., ...
& Hyde, K. D. (2020). Two new species of Termitomyces (Agaricales, Lyophyllaceae) from China and Thailand. Phytotaxa,
439:
231-242.