• Mycobiology
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• v.41 no.1
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• pp.25-36
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• 2013

Parmotrema A. Massal. is a common lichen genus scattered throughout the Korean Peninsula; however, no detailed taxonomic or revisionary study of this genus has been conducted for nearly two decades. Therefore, this study revised the taxonomy of this genus based on specimens deposited in the lichen herbarium at the Korean Lichen Research Institute and samples wereidentified using recent literature. In this revisionary study, a total of eighteen species of Parmotrema including eight new records [Parmotrema cetratum (Ach.) Hale, Parmotrema cristiferum (Taylor) Hale, Parmotrema grayanum (Hue) Hale, Parmotrema defectum (Hale) Hale, Parmotrema dilatatum (Vain.) Hale, Parmotrema margaritatum (Hue) Hale, Parmotrema pseudocrinitum (Abbayes) Hale, and Parmotrema subsumptum (Nyl.) Hale] are documented. Detailed descriptions of each species with their morphological, anatomical and chemical characteristics are also given and a key to the known Parmotrema species of the Korean Peninsula is presented.

• Journal of Ecology and Environment
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• v.38 no.4
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• pp.493-503
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• 2015

This study analyzed how spatial distribution of Himantormia lugubris is affected by the microenvironment in the Antarctic Specially Protected Area (ASPA) No. 171 located in the Barton Peninsula of King George Island that belongs to the maritime Antarctic. In order to determine the population structure of H. lugubris growing in Baekje Hill within ASPA No. 171, we counted the individuals of different size groups after dividing the population into 5 growth stages according to mean diameter as follows: ≤ 1 cm, 1-3 cm, 3-5 cm, 5-10 cm, and ≥ 10 cm. The count of H. lugubris individuals in each growth stage was converted into its percentage with respect to the entire population, which yielded the finding that stages 1 through 5 accounted for 32.8%, 25.3%, 15.9%, 22.5%, and 3.5%, respectively. This suggests that the population of H. lugubris in ASPA No. 171 has a stable reverse J-shaped population structure, with the younger individuals outnumbering mature ones. The mean density of H. lugubris was 17.6/0.25 m², mean canopy cover 13.3%, and the mean dry weight 37.8 g/0.25 m². It began to produce spore in the sizes over 3 cm, and most individuals measuring 5-10 cm were adults with sexually mature apothecia. The spatial distribution of H. lugubris was highly heterogeneous. The major factors influencing its distribution and performance were found to be the period covered by snow, wind direction, moisture, size of the substrate, and canopy cover of Usnea spp. Based on these factors, we constructed a prediction model for estimating the spatial distribution of H. lugubris. Conclusively, the major factors for the spatial distribution of H. lugubris were snow, wind, substrate and the competition with Usnea spp. These results are important for understanding of the distribution in the maritime Antarctic and evolution of H. lugubris that claims a unique life history and ecological niche.

• 한국균학회소식:학술대회논문집
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• 2006.10a
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• pp.24-28
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• 2006

Author have studies lichen flora of the most important ice-free areas of Continental Antarctic: Bunger Hills, and the vicinity of Prudz Bay (Larsemann Hills, and Radok Lake in Prince Charles Mountains). Totally 44 lichen species from 22 genera were reported for Bunger Hills and 50 lichen species from 22 genera and 10 families: Acarosporaceae, Lecanoraceae, Lecideaceae, Parmeliaceae, Pertusariaceae, Physciaceae, Rhizocarpaceae, Stereocaulaceae, Theloschistaceae, and Umbilicariaceaewere reported for the Prudz Bay Region. 20 lichen species were found in the region for the first time. Phytogeographic analysis indicated a relatively high proportion of species with bipolar distribution - about 50% of recorded lichen species. About 30% of lichens normally don't extend into maritime zone occurring in continental Antarctic only. The most common lichen families in the region are Buelliaceae, Lecanoraceae and Teloschistaceae. The water supply and not a temperature is the critical factor for lichens in the Continental Antarctic. Moisture appears to be supplied for lichens not only from snow-melt water but mainly from air. In Maritime Antarctic, due to high air humidity macrolichens form communities everywhere (Himantormia, Usnea and Umbilicaria). In oases of Continental Antarctic extensive sites are lacking in lichen cover, even if the ground is normally snow free. Lichens occur at humid sites with moisture which were brought by winds over the ice cap and poorly developed or absent in dry areas. Of particular significance for lichens are substrate characteristics, animals influence and salinity brought by wind in coastal areas. Most rich lichen vegetation developed in oases around nests of snow petrels, where the melt water is enriched by nutrients. In contrast, the most pure vegetation is on mobile sand and gravel and in salted coastal habitats.