Mycologia
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Soil ascomycetes from Spain. XII. Ascotricha
canariensis sp. nov.
Alberto M. Stchigel, Josep Guarro, Dania García Sánchez & Begoña Acosta
Hernández
To cite this article: Alberto M. Stchigel, Josep Guarro, Dania García Sánchez & Begoña Acosta
Hernández (2000) Soil ascomycetes from Spain. XII. Ascotricha�canariensis sp. nov., Mycologia,
92:4, 805-809, DOI: 10.1080/00275514.2000.12061222
To link to this article: https://doi.org/10.1080/00275514.2000.12061222
Published online: 04 Jun 2019.
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Mycologia, 92(4), 2000, pp. 805-809.
© 2000 by The Mycological Society of America, Lawrence, KS 66044-8897
Soil ascomycetes from Spain. XII. Ascotricha canariensis sp. nov.
Alberto M. Stchigel 1
Josep Guarro
sealed with a rubber band and labelled. On returning to
the laboratory soil was stored at 4-7 C until used. Approx
1 g of the sample was treated with 60% (v/v) ethyl alcohol
for 10 min (after Warcup and Baker 1963). The supernatant was discarded and the solid phase was suspended in 10
mL of distilled water. The suspensions were cultured on
potato carrot agar (PCA) with chloramphenicol (50 mg/L)
at room temperature (22-25 C) under 12 h of darkness
alternating with 12 h of cool white fluorescent light. The
morphological characteristics of the colonies were studied
on malt extract agar (MEA; Difco), oat meal agar (OMA;
Difco), PCA, and potato dextrose agar (PDA, Difco) at 10,
15, room temperature (22-25), 37 and 42 C, under 12 h of
darkness alternating with 12 h of cool white fluorescent
light. Color notations in parentheses are from Kornerup
and Wanscher (1984). The measurements of the fungal
structures were taken in water or lactophenol. Photomicrographs were obtained with a Leitz Dialux 20 EB microscope.
Scanning electron microscopy techniques were described
previously by Figueras and Guarro (1988).
Unitat de Microbiologia, Facultat de Medicina i
Ciencies de la Salut & /nstitut d'Estudis Avanc;ats,
Universitat Rovira i Virgili, C/Sant Llorenc;, 21,
43201 Reus, Spain
Dania Garcia Sanchez
Instituto de Investigaciones Fundamentales en
Agricultura Tropical "Alejandro Humboldt, " C/ 1 esq.
2, Santiago de las l-egas, Ciudad de la Habana, Cuba
Begoiia Acosta Hernandez
Departamento de Patologia Animal, Producci6n
Animal, Bromatologia y Tecnologia de los Alimentos,
Facultad de Veterinaria de Las Palmas de Gran
Canaria, Spain
Abstract: Ascotricha canariensis sp. nov. (Xylariaceae, Ascomycetes) isolated from soil of the Canary
Islands is described and illustrated. It belongs to the
group of Ascotricha species with cylindrical asci and
is differentiated from the other species by bearing
ascomata with short, single or once-branched setae
and by the presumed absence of an anamorph.
Key Words: Ascomycota, soil fungi, Xylariales
Ascotricha canariensis Stchigel, D. Garcia et Guarro,
sp. nov.
FIGs. 1-9
Mycelium ex hyphis subhyalinis vel brunneis, ramosis,
septatis, levibus vel tuberculatis, 1-6 11m diam composito.
Coloniae in agaro cum decocto tuberorum et carotarum
"PCA" restrictae, planae, tenues, ex mycelio vegetativo submerso, subhyalinae vel brunneae; reversum olivaceo-brunneo vel nigrum. Ascomata superficialia vel immersa, ostiolata, translucida, olivaceo-brunnea vel atro-brunnea, subglobosa vel globosa, 160-180 x 140-160 IJ.m, apex cum collo brevi, 12-25 11m alta, 25-40 11m lata, pilosa. Pili
rigidiusculi, non ramosi vel 1-ramosi, verrucosi, septati,
atrobrunnei, 15-45 11m longi, 3-5 11m diam ad basim, cum
vesicula hyalina et globosa vel piriformia, laevia, 3-5 11m
diam, ad apicem formanti. Peridium parum olivaceo-brunneum vel brunneum, tenue, ex textura epidermoidea vel
intricata, 4-6 stratiorum compositum, 10-15 11m crassitunicatum. Asci 47-54 X 5-7 !J.m, lineari-cylindrici, stipitati,
cum muris tenuibus, deliquescenti, octospori. Paraphyses
ovoideae vel
nullae. Ascosporae 6-8 X 4.5-6 X 2-4 ~J.m,
ellipsoideae, oblatae, atro-brunneae, laeves, fissura germinali aequatoriale paratae, uniseriatae. Status conidialis nullis.
During the course of a study of soil ascomycetes from
Spain, an interesting species of Ascotricha Berk. was
isolated from Gran Canaria, Canary Islands, located
near the African continent in the Atlantic Ocean. Its
origin is volcanic and it has a surface area of 100.55
km 2 • The terrain is basically basaltic, and the vegetation is mainly composed of Phoenix spp., some Cactaceae, and numerous members of the Poaceae. The
area has a Mediterranean climate. The average summer temperature is 22 C, ranging 17-25 C. The mean
annual precipitation is 150-200 mm. The morphological characteristics differentiate this taxon from all
previously described species in the genus (Hawksworth 1971, Udagawa et al 1994a, b, Stchigel and
Guarro 1998, Udagawa and Uchiyama 1999) and is
thus described here as new.
Mycelial hyphae subhyaline to brown, branched,
septate, smooth to tuberculate, 1-6 1-1m diam. Colonies on PCA growing slowly, attaining 17-20 mm
diam in 14 d at room temperature, olive brown (M.
4F5) to blackish, flat, thin, powdery to granulose,
consisting of submerged mycelium and sparse aerial
hyphae, producing abundant ascomata; reverse olive
Materials and methods.-Soil was mainly collected from the
Ao horizon with sterilized polyethylene bags. These were
Accepted for publication February 28, 2000.
1 Email: ams@astor.urv.es
805
Published online 04 Jun 2019
806
MYCOLOGIA
FIGS. 1-6. Ascotricha canariensis. 1. Ascoma. 2. Detail of the peridium. 3. Simple and branched setae. 4. Asci and ascospores. 5. Asci and ascospores; ascospore showing the germ slit (arrow). 6. Ascospores (SEM). Bars: 1 = 50 f.Lm; 2-6 = 10 f.Lm.
807
STCHIGEL ET AL: NEW ASCOTRICHA SPECIES
FIGS. 7-9.
Ascotricha canariensis. 7. Ascoma. 8. Ascus with ascospores. 9. Ascospores. Bars: 7
= 25
JLm; 8, 9
= 10 JLID.
808
MYCOLOGIA
brown (M. 4F5) to blackish; ascomal initials coiled.
Ascomata superficial to immersed, scattered to
grouped, ostiolate, subglobose to globose, translucent, olive-brown to dark brown, 160-180 X 140-160
JJ.m, sometimes with a short beak 12-25 X 25-40 JJ.m.
Setae stiff, simple or bifurcate at the middle, 2-3 septate, verrucose and dark brown at the base, becoming
smooth and hyaline at the apex, 15-45 JJ.m long, 35 JJ.m diam at the base, thin-walled, terminated by a
hyaline, globose to pyriform, smooth-walled vesicle,
2.4-4 JJ.m diam. Peridium 4-6 layered, 10-15 JJ.m
thick, pale olivaceous-brown to brown, textura epidermoidea to intricata in surface view. Asci 47-54 X 57JJ.m, spore-bearing part 35-48 JJ.m long, cylindrical,
short stipitate, thin-walled, evanescent, fasciculate, 8spored, without apical structures. Paraphyses not observed. Ascospores 6-8 X 4.5-6 X 2-4 JJ.m, ovoid to
ellipsoidal in front view, oblate, dark brown, smoothwalled, with an equatorial germ slit on the narrow
side, uniseriate. Anamorph not observed. On OMA at
room temperature, colonies attaining 20-22 mm
diam in 14 d, similar to those on PCA but strongly
zonate. On MEA at room temperature, colonies attaining 15-16 mm diam in 14 d, raised, cottony,
white; exudate absent; soluble pigment orange; reverse orange (4B6). Ascomata not formed. On PDA
at room temperature, colonies attaining 19-21 mm
diam in 14 d, similar to those on MEA but without a
soluble pigment and reverse whitish. Ascomata not
formed. On PCA, OMA, MEA and PDA at 15 and 37
C, growing very slowly, attaining 3-4 mm diam in
14 d, raised, hairy, white. Ascomata not produced. No
growth was observed at 10 and 42 C.
Specimens examined. SPAIN. GRAN CANARIA: La Laguna
(28° 9' N, 15° 25' W), from soil, 22-VIII-1998, col. B. Acosta,
isol. A. M. Stchigel (HOLOTYPE IMI 381334, ISOTYPE
FMR 6738). Living cultures ex type: CBS 102197, FMR 6738,
IMI 381334.
Discussion.-The genus Ascotricha encompasses 13
species (Ames 1951, Hawksworth 1971, Kulshreshtha
et al 1977, Stchigel and Guarro 1998, Udagawa et al
1994a, b, Udagawa and Uchiyama 1999), characterized by ostiolate or nonostiolate setose ascomata with
translucent peridial wall, 8-spored asci, brown ellipsoidal ascospores with an equatorial germ slit, and
anamorphs belonging to Dicyma Boulanger or to the
Geniculosporium-Nodulisporium complex. Ascotricha
spp. are generally found on cellulosic substrates
(Ames 1951, Hawksworth 1971, Calviello 1978), dung
(Hawksworth 1971, Kahn and Cain 1977) and soil
(Hawksworth 1971, Horie et al 1993, Stchigel and
Guarro 1998, Udagawa et al 1994a, b). The genus
Ascotricha, morphologically very close to Chaetomium
Kuntze, was erected by Berkeley (1838) for A. char-
tarum Berk. Hawksworth (1971), in an extensive review of the genus, considered it included in the
Chaetomiaceae of the order Sphaeriales although
some similarities with members of the Coniochaetaceae were later noticed (Hawksworth and Wells
1973). Khan and Cain (1977) considered Ascotricha
as phylogenetically distant from Chaetomium and related genera, and placed it in the Xylariaceae.
Laess0e (1994) considered Ascotricha and the closely
placed Ascotrichella Valldosera & Guarro (Valldosera
and Guarro 1988) as genera incertae sedis due mainly
to the nonstromatic nature of their ascomata, which
differentiated them from the other genera of the Xylariaceae. Ascotricha was recently included in the Xylariaceae (Hawksworth et al 1995, Eriksson and
Hawksworth 1998), and this view has been substantiated by Lee and Hanlin (1999) on the basis of ISS
rDNA sequence analyses. Ascotricha canariensis belongs to the group of species with cylindrical asci
which includes A. amesii Hawksworth, A. amphitricha
(Corda) S.]. Hughes, A. bosei Hawksworth, A. chartarum Berk., A. delhiana Kulshreshtha, Raychardhuri
& Khan, A. erinacea Zambett., A. guamensis Ames, A.
hispanica Stchigel & Guarro, A. lusitanica Kenn. and
A. xylina Ames. It can be easily differentiated from
all previously described species (with the exception
of A. hispanica) mainly by the setal morphology and
by the presumed absence of an anamorph. Ascotricha
hispanica also has short and simple ascomal setae and
lacks an anamorph, but differs from A. canariensis by
its longer (30-100 X 3-5 JJ.m) setae with a more elaborate branching pattern (sub-dichotomous and onceto twice-branched) and by its smaller ascospores
(4.5-7 X 3-4 X 3-4 JJ.m).
Acknowledgements.-This work was supported by a grant
from the Fundaci6 Ciencia i Salut, Reus, Spain. The authors
are indebted to to Dr. E. Descals for helpful comments. The
senior author is grateful for a fellowship from the Universitat Rovira i Virgili (U.R.V.), Catalonia, Spain.
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