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Mycologia, 95(6), 2003, pp. 1218-1226.
© 2003 by The Mycological Society of America

Apiosordaria antarctica and Thielavia antarctica, two new ascomycetes from Antarctica


Alberto M. Stchigel 1
Josep Guarro

     Unitat de Microbiologia, Facultat de Medicina i Ciències de la Salut, C/ Sant Llorenç 21, 43201 Reus, Tarragona, Universitat Rovira i Virgili, Tarragona, Spain

Walter Mac Cormack

     Instituto Antártico Argentino, Departamento de Biología, C/ Cerrito 1248 (1010), Buenos Aires, Argentina

    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 TAXONOMY
 LITERATURE CITED
 

Two new species of ascomycetes, Apiosordaria antarctica, isolated from soil, and Thielavia antarctica, isolated from a sample of the lichen Usnea cf. aurantio-atra, both collected on King George Island (Antarctica), are described and illustrated. Apiosordaria antarctica is characterized by ostiolate ascomata with agglutinated hairs, eight-spored, uniseriate and cylindrical asci, and two-celled, irregularly navicular ascospores, with an upper cell ornamented with very small warts and with an apical germ pore. Thielavia antarctica is characterized by nonostiolate ascomata, with a thick peridium, eight-spored, cylindrical asci, uniseriate, oblate, ovoid ascospores, a slightly protruding apical germ pore, and a phialidic anamorph.

Key words: Chaetomiaceae, Lasiosphaeriaceae, lichenicolous fungi, soil-borne fungi, Sordariales, systematics


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 TAXONOMY
 LITERATURE CITED
 
During more than a century of mycological studies in Antarctica, few fungal taxa have been reported from soil and lichens, only a small number of which are ascomycetes. These taxa are showed in Table I. The scientific expedition of the Instituto Antártico Argentino in 1996 visited King George Island, and one of us (WMC) collected numerous samples of soil, plants, lichens, wood and marine sediments. Two ascomycetes isolated from soil and a lichen were sufficiently different from all previously described taxa to warrant the proposal of new species of Apiosordaria Arx & Gams and Thielavia Zopf, respectively. In this report, the species are described and illustrated.


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TABLE I. Ascomycetes reported from Antarctic lichens and soil samples

 

    MATERIALS AND METHODS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 TAXONOMY
 LITERATURE CITED
 
Soil samples and lichens were collected around the Jubany Argentinian base and in Three Brothers Hill (both at 62° 14'S, 58° 39'W), on King George Island (between 61° 49' 54''S and 62° 17' 13''S, and 57° 26'' 11''W and 59° 6'' 55''W). King George Island is part of the South Shetland archipelago and has an area of 1295 km2. Less than 10% of the surface is ice free during the summer. The terrain is basaltic and composed of meteorized rocks, and penguin and skua dung is common. The vegetation is mainly algae, such as Prasiola crispa, lichens (including Acarospora molybdina, Lecidea auriculata, Placodium spp.), mosses (Andreaea depressinervis, A. regularis, Brachytecium antarcticum, Bryum dichotomum, Grimnia antartici, Hypnum sarmentosum, Pogonatum alpinum, Tortula excelsa, etc.) and a few herbaceous plants (Colobanthus quitensis, Deschampsia antarctica and Poa pratensis) (Cabrera 1994Citation, Lindsay 1971Citation, Möller and Dreyfuss 1996Citation). The area is dominated by a cold climate. The climatological data include: average temperature, -2.1 C (min -20.0 C, max +10.0 C); total annual precipitation, 800 mm (mostly in the form of snow); minimum, average and maximum atmospheric pressure, 946 mb, 989.9 mb and 1025 mb, respectively; average humidity, 89%. Soil samples were collected from the A horizon and lichen samples directly from the rock surface, placed in sterilized polyethylene bags, closed by rubber band and stored in a refrigerator at -20 C.

Approximately 1 g of each soil sample was suspended in 5 mL of 5% v/v acetic acid, shaken vigorously for 5 min and left for an additional 5 min. The layer of acetic acid was removed by decantation, the residual soil was resuspended in 9 mL of sterilized water and plated in a Petri dish. Potato-carrot agar with chloramphenicol (PCA; grated potatoes, 20 g; grated carrot, 20 g; agar-agar, 20 g; chloramphenicol, 50 mg; tap water, 1 L) was placed on top of the soil suspension and mixed. All cultures were incubated at 10 ± 1 C for 12 h in the dark, alternating with 12 h under a cool white fluorescent light.

Lichen samples were cut into small pieces (approx. 5 mm long) with sterile surgical steel blades and dissection clamps. The pieces were placed on the surface of Petri dishes with tap-water agar (TWA; agar-agar, 20 g; tap water, 1 L), and incubated at 10 ± 1 C for 12 h in the dark, alternating with 12 h under cool white fluorescent light.

The strains were grown on oatmeal agar (OMA; oatmeal 30 g; agar-agar, 20 g; tap water, 1 L) and PCA (without chloramphenicol) at 35 C, at room temperature (approx. 25 C), at 15 C and at 5 C for 12 h in the dark, alternating with 12 h under a cool white fluorescent light. Color notations in parentheses are from Kornerup and Wanscher (1984)Citation. The structures were measured in lactophenol.


    TAXONOMY
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 TAXONOMY
 LITERATURE CITED
 
Apiosordaria antarctica Stchigel et Guarro, sp. nov. Figs. 1–10



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FIGS. 1–5. Apiosordaria antarctica FMR 6675. 1. Ascoma. 2. Detail of the peridial surface. 3. Agglutinated hairs. 4. Ascus and young ascospores. 5. Ascospores. Scale bars: 1 = 100 µm, 2–5 = 20 µm

 

[Mycelium ex hyphis olivaceo-brunneis, septatis, ramosis, levis, 1–3 µm diametro composita. Coloniae in PCA expansae, planae, ex mycelio vegetativo submerso et aereo, olivaceo-brunnea; reversum olivaceo-brunneum. Ascomata superficialia, ostiolata, atrobrunnea, pyriformia, 530–700 x 320–350 µm, cum collum papillatum, 260–400 x 240–260 µm; pilis conglutinatis, septatis, fasciculatis, ex cellulis dilute brunneis vel brunneis, 7–10 x 3–7 µm composita. Peridium 6–9 stratiorum compositum, ex textura angularis, brunneum. Asci 8-spori, cylindrici, 165–180 x 8–10 µm. Paraphysis nullis. Ascosporae uniseriatae, primum unicellulares, hyalinae et verrucosae, deinde brunneae, transverse septatae ad bicellularis; cellula superiore irregulariter naviculare, atrobrunnea vel nigra, 19–24 x 8–10 µm, verruculosae, cum foramine germinali singulari apicali praedita, 1 µm diam; cellula inferiore subhyalinae vel subbrunnea, conica, 3.5–4.5 x 3.5–4 µm, levae. Status conidialis nullis.]

Mycelium composed of olivaceous-brown, septate, branched, smooth, 1–3 µm diam hyphae. Colonies on PCA 67–71 mm diam within 7 d at room temperature (ca 25 C), flat, felty, consisting of submerged mycelium and sparse aerial hyphae, olive brown (4F8), producing abundant ascomata; reverse olive brown (4F8); ascomatal initials originating as coiled hyphae of vegetative mycelium soon interwoven by neighboring hyphae. Ascomata superficial, scattered, ostiolate, dark brown, pyriform, 530–700 x 320–350 µm, setose, with a distinctive neck; neck papillate, conical, 260–400 x 240–260 µm; ascomatal hairs agglutinated, spread along the neck, consisting of septate, fasciculate, pale brown to brown cells measuring 7–10 x 3–7 µm. Peridium 6–9 layered, 14–17 µm thick, textura angularis, brown; external cells polygonal, measuring 6–25 µm diam. Asci 8-spored, fasciculate, cylindrical, 165–180 x 8–10 µm, apex flattened, with a conspicuous apical ring. Paraphyses absent. Ascospores uniseriate, one-celled, hyaline and verrucose when young, becoming dark brown, two-celled by the formation of a transverse septum when mature; upper cell irregularly navicular, truncate and darkened at the base, dark brown to black, 19–24 x 8–10 µm, ornamented with small warts, with conspicuous apical, 1 µm diam germ pore; lower cell subhyaline to light brown, conical, 3.5–4.5 x 3–4 µm, smooth. The apical ascospore sometimes appearing inverted with respect to the others. Anamorph unknown.

Colonies on OMA attaining more than 70 mm diam within 7 d at room temperature, similar to those on PCA; ascomata abundant. Colonies on OMA 41–45 mm diam within 7 d at 15 C, flat, olive brown (4D6); reverse the same color. Colonies on PCA and OMA <10 mm diam within 7 d at 5 C; ascomata not produced. No growth at 35 C.

[Specimens examined. ANTARCTICA. King George Island: Jubany Argentinian base, from soil, 11-XI-1996, col. W. Mac Cormack, isol. A. M. Stchigel (holotype: IMI 381338, isotype: FMR 6675. Living cultures: CBS 101.966, FMR 6675, IMI 381338).]

Apiosordaria (Lasiosphaeriaceae, Sordariales) was proposed by von Arx and Gams (1967)Citation. It is characterized by pale or dark, operculate ascomata, nonamyloid asci lacking distinct apical structures, and two-celled ascospores, with a dark and ornamented upper cell and a lower hyaline or paler cell. Later, Krug et al (1983)Citation considered the two morphologically similar genera Echinopodospora Robinson and Lacunospora Cailleux as synonyms of Apiosordaria. The genus currently comprises 20 species (Krug et al 1983Citation, Guarro and Cano 1988Citation, Udagawa 1990Citation, Mukerji et al 1995Citation, Stchigel et al 2000Citation), most of them reported from soil.

Apiosordaria antarctica resembles A. otanii Udagawa (1990)Citation by the presence of agglutinated hairs and ascospores with a warted wall. However, the ascomata of A. otanii have an inconspicuous to short neck, with long hypha-like hairs, and its ascospores are broader (15–18 µm). The anamorph of A. otanii is chrysosporium-like.

Thielavia antarctica Stchigel et Guarro, sp. nov. Figs. 11–22



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FIGS. 11–15. Thielavia antarctica FMR 7920. 11. Ascomatal initials. 12. Detail of the ascomatal wall. 13. Asci and young ascospores. 14. Ascospores. 15. Anamorph. Scale bars = 20 µm

 

[Mycelium ex hyphis hyalinis vel dilute brunneis, septatis, ramosis, levis, 1–20 µm diam composita. Coloniae in PCA expansae, floccosae, hyalinae; reversum hyalinum. Ascomata superficialia, non-ostiolata, glabra, atrobrunnea, globosa, 250–450 µm diam. Peridium 5–8 stratiorum compositum, ex textura epidermoidea et textura intrincata, dilute brunneum. Asci 8-spori, cylindrici, 40–65 x 7–11 µm. Paraphysis nullis. Ascosporae uniseriatae, unicellulares, brunneae, crassae ovoideae et complanatae, 9–11 x 8–10 x 6.5–7 µm, levae, cum foramine germinali singulari apicali praedita. Anamorphosis Paecilomyces similis.]

Mycelium composed of hyaline to pale brown, septate, branched, anastomosing, smooth-walled, 1–20 µm wide hyphae. Colonies on PCA, attaining 63–65 mm diam within 14 d at 15 C, cottony, white, producing abundant ascomata after 2 mo; reverse uncolored; ascomatal initials originating as coiled hyphae of vegetative mycelium. Ascomata superficial (rarely immersed), scattered, nonostiolate, glabrous, dark brown, globose, 250–450 µm, covered with abundant hyaline hyphae. Peridium 5–8 layered, 12–30 µm thick, textura epidermoidea to intrincata, light brown, with irregularly polygonal dark brown zones up to 60 µm diam; external cells measuring 5–25 µm diam. Asci eight-spored, nonfasciculate, cylindrical, 40–65 x 7–11 µm, inconspicuously stipitate, without apical structures. Paraphyses absent. Ascospores uniseriate, one-celled, brown, broadly ovoid and bilaterally flattened, 9–11 x 8–10 x 6.5–7 µm, smooth-walled, with a slightly protruding apical germ pore, to 1 µm diam. Anamorph Paecilomyces-like. Conidia one-celled, hyaline, produced in dry chains, obovoid with a truncate base, 3.5–5 x 1.5–2.5 µm, smooth-walled. Phialides borne terminally or laterally on the vegetative hyphae, usually solitary, rarely forming verticils of 2–3 phialides hyaline, flask-shaped to needle-shaped, 15–45 x 1.5–3 µm, tapering toward the tips; collarette inconspicuous.

Colonies on OMA at 15 C, similar to those on PCA; ascomata and anamorph abundant. Colonies on OMA and PCA at 25 C, similar to those on PCA at 15 C; ascomata not produced. Colonies on PCA and OMA at 5 C, with a very slow growth (<10 mm); ascomata not produced. No growth at 35 C.

[Specimens examined. ANTARCTICA. King George Island: Three Brothers Hill, from Usnea cf. aurantio-atra, 22-XI-1996, col. W. Mac Cormack, isol. A. M. Stchigel (holotype: IMI 389346, isotype: FMR 7920. Living cultures: FMR 7920, IMI 389346).]

Species of Thielavia Zopf (Chaetomiaceae, Sordariales) have a humicolous or fungicolous habit. The genus is characterized by spherical, glabrous or setose, nonostiolate ascomata, having a thin peridium with textura epidermoidea; asci eight-spored, fasciculate or clustered, ellipsoidal, saccate or rarely more or less cylindrical; and ascospores one-celled, fusiform, ellipsoidal, slightly clavate or ovoid, brown, with a conspicuous, terminal or lateral germ pore; and occasionally with aleurioconidia. This genus was monographed by Mouchacca (1973)Citation, Malloch and Cain (1973)Citation and von Arx et al (1988)Citation. It currently contains 18 species (von Arx et al 1988Citation, Chen and Chen 1996Citation, Ito et al 1998Citation, Stchigel et al 2002Citation). Other genera that are related morphologically are compared in Table II.


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TABLE II. Comparison between Thielavia antarctica and relaxed taxa

 
Thielavia antarctica has morphological features reminiscent of Thielavia, i.e., translucent peridium with textura epidermoidea, and Melanocarpus, i.e., opaque, ovoid and bilaterally flattened ascospores. The nature of the peridium distinguishes T. antarctica from Melanocarpus (von Arx 1975Citation). Moreover, T. antarctica has cylindrical asci, which are present in Thielavia tortuosa Udagawa & Sugiyama, and phialoconidia similar to those seen in Thielavia terrestris (Apinis) Malloch & Cain. Both characters, although exceptional in Thielavia, in which ellipsoidal or saccate asci and aleurioconidia typically are formed, are absent in Melanocarpus, in which cylindrical-saccate asci and arthroconidia are typical. However, Thielavia tortuosa and T. terrestris differ from T. antarctica in having sinuous asci and large and fusiform ascospores, with a subterminal to lateral germ pore and clavate asci and small and pyriform ascospores, respectively. On the basis of the shape of the ascospores, the species closest to Melanocarpus are M. albomyces (Cooney & Emerson) Arx and M. oblatus Guarro & Aa. However, M. albomyces has bigger ascospores (13–16 x 11–14 x 9–11 µm) and ascospores of M. oblatus are circular in face view (ovate in T. antarctica).



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FIGS. 6–10. Apiosordaria antarctica FMR 6675. 6. Ascus. Observe the inverted position of the upper ascospore inside the asci. 7. Young ascospores inside the asci. 8. Cell wall ornamentation of the young ascospores. 9–10. Mature ascospores under SEM. Scale bars: 6, 8–10 = 10 µm, 7 = 20 µm

 


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FIGS. 16–22. Thielavia antarctica FMR 7920. 16. Ascomata. 17. Cross section of an ascoma. 18–19. Ascus with young ascospores. 20. Ascospores. 21. Catenate conidia. 22. Phialidic anamorph. Scale bars: 16 = 200 µm; 17 = 20 µm; 18–20 = 10 µm; 21 = 25 µm; 22 = 20 µm

 

    ACKNOWLEDGMENTS
 
The authors are indebted to the Instituto Antártico Argentino for its collaboration.


    FOOTNOTES
 
1 Corresponding author. E-mail: ams{at}astor.urv.es Back

Accepted for publication August 5, 2003.


    LITERATURE CITED
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 TAXONOMY
 LITERATURE CITED
 
Azmi OR, Seppelt RD., 1997 The broad-scale distribution of microfungi in the Windmill Islands region, continental Antarctica. Polar Biol 19:92-100

Cabrera AL., 1994 Regiones fitogeográficas Argentinas. Enciclopedia Argentina de agricultura y jardinería. Tomo II, fascículo 1, primera reimpresión. Buenos Aires: Acme ed

Chen KY, Chen ZC., 1996 Thielavia pingtungia sp. nov., a thermophilic ascomycete from Taiwan. Mycotaxon 60:241-247

Del Frate G, Caretta G., 1990 Fungi isolated from Antarctic material. Polar Biol 11:1-7

Ellis MB., 1980 Thermophilous fungi isolated from some Antarctic and sub-Antarctic soils. Mycologia 72:1033-1036

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Malloch D, Cain RF., 1973 The genus Thielavia. Mycologia 65:1055-1077

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———, ———, Mac Cormack W, Guarro J., 2001 Antarctomyces psychrotrophicus gen. et sp. nov., a new ascomycete from Antarctica. Mycol Res 105:377-382

———, Figuera L, Cano J, Guarro J., 2002 New species of Thielavia, with a molecular study of representative species of the genus. Mycol Res 106:975-983

Sugiyama J., 1970 World's last frontier III: polar mycology in Antarctica. Polar News 6:17-24

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———, Gams W., 1967 Über Pleurage verruculosa und die zugehörige Cladorrhinum-Konidienform. Nova Hedwigia 13:199-208

Zucconi L, Pagano S, Fenice M, Selbmann L, Tosi S, Onofri S., 1996 Growth temperature preferences of fungal strains from Victoria Land, Antarctica. Polar Biol 16:53-61





This Article
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