Summary / 要旨(PDF) - 植物研究雑誌 THE JOURNAL OF

J. Jpn. Bot. 91 Suppl.: 376–387 (2016)
Two New Species of Ramalina (Ramalinaceae, Ascomycota)
from Korea
Kwang Hee Moona, Chorong Ahna, Jeong Eun Hana
and Hiroyuki Kashiwadanib,*
a
National Institute of Biological Resources, 42, Hwangyeong-ro, Seo-gu, Incheon, 22689 KOREA;
b
Department of Botany, National Museum of Nature and Science,
4-1-1, Amakubo, Tsukuba, 305-0005 JAPAN
*Corresponding author: [email protected]
(Accepted on January 9, 2016)
Two new species, Ramalina intestiniformis Kashiw. & K. H. Moon and R.
sphaerophora Kashiw. & K. H. Moon, are described from Korea. Ramalina intestiniformis,
a maritime species, resembles R. almquistii Vain., but it differs by having irregularly but
totally inflated lobes throughout the branches, continuous medullary hyphae, and shortly
fusiform ascospores. Ramalina sphaerophora resembles R. kurokawae Kashiw. and R.
yasudae Räsänen, but it differs in having semi-corticate spherical nodules instead of
soralia. Both species are known only from Korea up to now.
Key words: Korea, lichens, new species, Ramalina intestiniformis, Ramalina sphaerophora.
The genus Ramalina (Lichenized
Ascomycetes, Lecanorales) is a well-known
fruticose lichen widely distributed in eastern
Asia and which comprises about 250 species in
the world. In Korea, 18 species had been listed
under the genus as of 2013 (Moon 2013).
In the course of our taxonomic study of the
genus Ramalina based on extensive collections
from Korea, we found the following two new
species and provide their descriptions herein:
Ramalina intestiniformis is a saxicolous
species found in coastal areas in Korea. It is
characterized by a decumbent to caespitose
thallus, sparingly and irregularly branched
branches growing from a broad base, irregularly
inflated fistulose lobes with perforations, absence
of soredia, medullary hyphae closely attached
to the inner walls of cortices, shortly fusiform
ascospores, and the presence of divaricatic
acid as a major chemical substance. Ramalina
sphaerophora is also a saxicolous species found
on maritime rocks and is easily recognized by
having irregularly branched thalli growing from
a common holdfast, up to 2 cm high, more or
less flattened and weakly inflated branches
ending in semi-corticate spherical nodules, and
by the production of evernic and obtusatic acids.
Both species seem to be endemic to Korea up to
now.
To confirm the taxonomic status of
these two new species in comparison with
morphologically similar species in the genus
Ramalina, the sequence of internal transcribed
spacer (ITS) regions of rDNA was applied in
this study. The ITS ribosomal DNA region is
a suitable universal DNA barcode marker for
fungi (Schoch et al. 2012).
—376—
386
The Journal of Japanese Botany Vol. 91 Centennial Memorial Issue
2: 113–118.
Hall T. A. 1999. BioEdit: a user-friendly biological
sequence alignment editor and analysis program for
Windows 95/98/NT. Nucleic Acids Symposium Ser.
41: 95–98.
Hecker K. H. and Roux K. H. 1996. High and low
annealing temperatures increase both specificity and
yield in touchdown and stepdown PCR. Biotechniques
20: 478–485.
Huelsenbeck J. P. and Ronquist F. 2001. MrBAYES:
Bayesian inference of phylogenetic trees.
Bioinformatics 17: 754–755.
Joneson S., Kashiwadani H., Tschabanenko S. and Gage
S. 2004. Ramalina of the Kuril Islands. The Bryologist
107: 98–106.
Kashiwadani H. 1996. Ramalina kurokawae Kashiw., a
new lichen species from Japan. Bull. Natn. Sci. Mus.
Ser. B 22: 55–57.
Krog H. and James P. W. 1977. The genus Ramalina in
Fennoscandia and the British Isles. Now. J. Bot. 24:
15–43.
Krog H. and Swinscow D. V. 1974. Ramalina species with
a hollow thallus (Fistularia) in East Africa. Now. J.
Bot. 21: 111–124.
Kurokawa S. and Kashiwadani H. 1982. Lichenes Rariores
et Critici Exsiccati. 11. National Science Museum,
Tokyo.
Larget B. and Simon D. L. 1999. Markov chain Monte
Carlo algorithms for the Bayesian analysis of
phylogenetic trees. Mol. Biol. Evol. 16: 750–759.
Moon K. H. 2013. Lichen-forming and Lichenicolous
Fungi of Korea. National Institute of Biological
Resources, Incheon.
Posada D. 2008. jModelTest: Phylogenetic model
averaging. Mol. Biol. Evol. 25: 1253–1256.
Schoch C. L., Seifert K. A., Huhndorf S., Robert V., Spouge
J. L., Levesque C. A., Chen W. and Fungal Barcoding
Consortium. 2012. Ribosomal internal transcribed
spacer (ITS) region as a universal DNA barcode marker
for Fungi. Proc. Nat. Acad. Sci. 109: 6241–6246.
Stamatakis A. 2014. RAxML Version 8: A tool for
phylogenetic analysis and post-analysis of large
phylogenies. Bioinformatics 30: 1312–1313.
Thompson J. D., Gibson T. J., Plewniak F., Jeanmougin F.
and Higgins D. G. 1997. The CLUSTAL_X windows
interface: flexible strategies for multiple sequence
alignment aided by quality analysis tools. Nucleic
Acids Res. 25: 4876–4882.
Vainio E. A. 1909. Lichenes in viciniis stationis hibernae
expeditionis Vegae prope pagum Pitlekai in Sibiria
septentrionali a Dre. E. Almquist collecti. Ark. Bot. 8:
11–175.
White T. J., Bruns T. D., Lee S. and Taylor J. 1990.
Amplification and direct sequencing of fungal
ribosomal RNA genes for phylogenetics. In: Innis M.
A., Gelfand D. H., Sninsky J. J. and White T. J. (eds.),
PCR Protocols. pp. 315–322. Academic Press, San
Diego.
文 光喜 a,A. Choronga,韓 定殷 a,柏谷博之 b:韓国
産カラタチゴケ属(カラタチゴケ科,子嚢菌門)の 2 新種
韓 国 か ら Ramalina intestiniformis Kashiw. & K. H.
Moon と R. sphaerophora Kashiw. & K. H. Moon の 2 新
種を記載した.
育するのに対し,後者はブナ帯~ハイマツ帯の日陰(多
くはオーバーハングした岩の下部)に生育する.韓国特
産種である.
1) Ramalina intestiniformis は海岸の垂直に近い北向き
の岩上に生育する.地衣体は匍匐またはやや下垂し,裏
2) R. sphaerophora は海岸の岩上に生育する.地衣体
は淡緑黄色であるが基物に付着する基部は黒褐色,裏
面のあちこちで基物にゆるく付着し高さ約 1.5 cm,径
3(–5) cm のクッション状.地衣体はわずかに枝分かれし,
枝は基部から先端まで不規則に膨らみ先端は短くとが
面 の あ ち こ ち で 基 物 に 固 着 し て 高 さ 1.0–1.5 cm, 径
1.0–2.0 cm のクッション状となる.枝は不規則に分枝し,
径 0.5–1.0(–2.0) mm.枝の大部分は中実であるが,膨ら
んだ部分に穿孔を生じる.粉芽や裂芽はないが,枝の先
端に球状の小塊を持つ.髄層の菌糸は連続,皮層の内壁
に密着する.子器は未見.地衣成分はエベルン酸,オブ
ツザート酸,ウスニン酸である.
り,中空,穿孔を有する,径は 0.5–2 mm.粉芽や裂芽
はない.髄層の菌糸は連続,皮層の内壁に密着する.子
器は枝の先端または側部に生じ,距はない.子器柄はく
2 室,
びれず,盤は初め凹むが後に隆起する.胞子は無色,
13–15 × 4–5 μm.地衣成分は地衣成分はジバリカート酸,
サラチン酸 (±),ウスニン酸である.
本種は R. almquistii Vain. に似ているが後者の枝は先
端部でふくれることがあっても大部分は偏圧され,髄層
の菌糸は集合して固まり皮層の内側はほとんど裸出す
るので区別できる.また,本種が海岸の岩上に限って生
本種は東アジア産の R. kurokawae Kashiw. に似てい
るが後者は粉芽を持ち,枝の基部が淡色である点で区
別できる.本種は東アジアに広く分布する R. yasudae
Räsänen と紛らわしいが,R. yasudae の地衣体は中実で
狭い基部から直立して灌木状となり,先端部や側部に粉
芽を生じ点で異なる.なお,R. yasudae にも球形の小塊
December 2016
Moon et al.: Two new Ramalina from Korea
が見られるが,これらは常に唇状の粉芽塊の中に生じ
る.北半球に広く分布する R. pollinaria (Westr.) Ach. も
本種に似ているが,枝は中実で粉芽を持つ点で区別でき
る.Krog and Swinscow (1974) は東アフリカから本種と
同様に枝の先端部に球形の小塊を持つ R. consanguinea
Müll. Arg. と R. tapperi Krog & Swinsc. を報告している.
しかしこれらは密に分枝した細い地衣体を持ちセッカ
酸やジバリカート酸を含むので異なる.本種が海岸の日
当たりのよい岩上に生育する.韓国特産種である.
387
カラタチゴケ属地衣類は地衣体の形態変異が大きく,
類縁種との区別が困難である場合が多い.今回記載した
2 種については,核リボゾーム遺伝子スペーサー領域
(nrDNA ITS) の塩基配列に基づく最尤法による系統樹を
作成して近縁種との関係を検討した.その結果,ここで
記載した 2 種は共に,近縁種とは独立したクレードを
形成し,既知種とは異なることが示唆された.
b
(a 韓国・国立生物資源館,
国立科学博物館植物研究部)