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Korean J. Pl. Taxon > Volume 56(2); 2026 > Article
SUN, CHUNG, PARK, and IM: A new record of Carpesium matsuei (Asteraceae) from Korea

Abstract

Carpesium matsuei Tatew. et Kitam. (Asteraceae) is reported from Mt. Gwangdeoksan in southwestern Korea for the first time. This species was previously known to be endemic to Japan. Carpesium matsuei is characterized by the following morphological characters: axillary, sessile heads forming raceme-like synflorescences; ovoid to globose involucres; and ovate basal leaves with acuminate apices and cordate bases. We propose a new Korean name, “Gwang-deok-dam-bae-pul,” based on the locality of the collection.

The genus Carpesium (Asteraceae) includes about 20 species, mainly found in Central and Eastern Asia. In Korea, seven species—C. abratanoides, C. glossopyllum, C. rosulatum, C. macrocephalum, C. divaricatum, C. cernuum, and C. triste—have been documented (Kim, 2020).
During a natural environment survey, we collected a species of Carpesium at the forest edge of Mt. Gwangdeoksan in Asan-si, southwestern Korea (Fig. 1). After reviewing the literature and herbarium specimens (KB and KH), we concluded that this plant is Carpesium matsuei Tatew. et Kitam., reported from Korea for the first time. It had been widely collected in mountainous regions of Korea and stored in herbaria as C. divaricatum.
Carpesium matsuei was originally described as an endemic species of Japan (Kitamura, 1936), and it was later classified as C. divaricatum var. matsuei (Tatew. et Kitam.) Kitam. (Kitamura, 1957). Since then, the taxonomic treatment of this taxon has been divided into two opinions: Carpesium matsuei Tatew. et Kitam. (Ohwi, 1965; Kato and Ebihara, 2011) and C. divaricatum var. matsuei (Tatew. et Kitam.) Kitam. (Iwatsuki et al., 1995; Ohashi et al., 2017).
Carpesium matsuei is characterized by the following characters: heads axillary, sessile, composing loose raceme-like synflorescences; involucres ovoid to subglobose; basal leaves ovate, apex acute to acuminate, base cordate. In contrast, the heads of C. divaricatum are solitary on each branch, and its basal leaves are ovate to ovate-oblong, apex obtuse to acute, and base rounded to truncate. In addition, the racemose synflorescences of C. matsuei better resemble those of C. abratanoides than those of C. divaricatum (Fig. 2, Table 1).
In a preliminary experiment, the chromosome number of 2n = 36 was observed in C. matsuei (a Korean population, unpublished data). The chromosome number differs from those reported in Japanese populations: C. matsuei (2n = 40, 40 + 2B, 40 + 3B) and C. divaricatum (2n = 40) (Cho, 1991). Variations in chromosome number within Carpesium have been noted in several taxa, such as C. abrotanoides L.: 2n = 36 in Hokkaido, Japan (Nishikawa, 1984); 2n = 40 and 40 + 2B in Tokyo, Japan (Cho, 1991); 2n = 36 in Mussoorie, India (Gupta et al., 2012); and 2n = 54 in Shanghai, China (Xu et al., 1992). Chromosome data plays an important role in Carpesium taxonomy and evolution. To better understand chromosome variation and its significance in C. matsuei, additional cytological and morphological studies are progressing well. Based on current morphological and cytological data, it appears more appropriate to treat this plant as a separate species rather than a variety of another species. The key morphological features of Korean Carpesium, including C. matsuei, are summarized (Table 1). We also provide a key to the Korean species of Carpesium.
Carpesium matsuei Tatew. et Kitam., Acta Phytotax. Geobot. 5: 27, 1936.—TYPE: JAPAN. Hokkaido: Ishikari Prov., Nopporo, 5 Sep 1935, M. Tatewaki (holotype: KYO).
Korean name: Gwang-deok-dam-bae-pul.
Carpesium divaricatum var. matsuei (Tatew. et Kitam.) Kitam., Mem. Coll. Sci. Kyoto Univ. Ser. B. 24: 48, 1957.
Herbs, perennial, stout, 30–100 cm tall. Rhizomes short, thick, stout. Stems erect, flexuous, divaricate in the upper part, densely pubescent with appressed fine hairs. Leaves radical and cauline; radical leaves withered before flowering; lower cauline leaves ovate, 9–20 × 6–14 cm, apex acute to acuminate, base cordate, margin irregularly shallow mucronate-toothed, both surfaces pubescent with tiny hairs, lower surface minute glandular-dotted; petiole shorter than blade, 8–12 cm long, narrowly winged only in the upper part; median leaves oblong, apex acuminate, base cuneate; upper leaves gradually smaller, sessile. Heads axillary, sessile on each branch, composing loose raceme-like synflorescences, nodding at flowering; involucres ovoid to subglobose, 5–6 × 6–9 mm; phyllaries in 3–4 series, scarious, imbricate; outer phyllaries broadly ovate, mucronate, about half the length of the inner phyllaries; inner phyllaries linear, apex obtuse, 5–8 mm long. Florets numerous, cylindric, 5-lobed, yellow; marginal florets female, 1.8–2 mm long; disc florets bisexual, 3–4 mm long. Achenes cylindric, ca. 3.5 mm long. (Fig. 2)
Flowering: July to October.
Distribution: Japan, Korea (Mt. Gwangdeoksan).
Specimens examined: KOREA. Gyeonggi-do: Gapyeonggun, Buk-myeon, Jeongmok-ri, Mt. Gangssibong, elev. 377 m, 21 Aug 2018, J. D. Lee et al. 18310-1 (KB); Gapyeonggun, Seolak-myeon, Mt. Yumyeongsan, elev. 980 m, 16 Aug 2007, W. K. Paik 940 (KH); 17 Aug 2007, W. K. Paik 377064-0130 (KB). Gangwon-do: Hwacheon-gun, Sane-myeon, Mt. Gwangdeoksan, Hoemok-ryeong, elev. 1,018 m, 15 Aug 2008, E. S. Jeon 80614 (KH); Hoengseong-gun, Dunnae-myeon, Hwadeok-ri, Mt. Taegisan, elev. 457 m, 25 Aug 2012, G. Y. Byeon et al. 110547 (KH); Hoengseong-gun, Dunnae-myeon, Mt. Cheongtaesan, elev. 739 m, 15 Oct 2011, S. J. Ji et al. L111530 (KH). Chungcheongbuk-do: Danyang-gun, Daegangmyeon, Oisan-ri, elev. 847 m, K. N. Jeon S2323-1467 (KB). Chungcheongnam-do: Asan-si, Songhak-myeon, Gangdan-ri, Mt. Gwangdeoksan, 22 Jul 2014, H.D. Son & E.M. Sun 233491 (CNU); 14 Aug 2025, H.T. Im & K.S. Chung 248900a, b (CNU). Gyeongsangbuk-do: Gimcheon-si, Buhang-myeon, Haein-ri, Mt. Minjujisan, elev. 900 m, 30 Sep 2011, H. J. Kim 110930-74 (KB); Gimcheon-si, Jeungsan-myeon, Pyeongchon-ri, Mt. Sudosan, elev. 519 m, 6 Aug 2018, Y. H. Jin & M. K. Lee JYH180806-17 (KB); Mungyeong-eup, Jungpyeong-ri, Mt. Daemisan, Heoriteo, elev. 650 m, 2 Sep 2012, B. U. Oh et al. 131936 (KH). Chungcheongnam-do, Cheonan-si, Mt. Gwangdeoksan, 26 Jul 2001, G. W Park & J. Y. Kim 018468 (KH). Jeollabuk-do: Jangsu-gun, Jyenam-myeon, Mt. Baekhwasan, 5 Sep 1999, B. U. Oh et al. (KH). Jeollanam-do: Gurye-gun, Ganjeonmyeon, Jungdae-ri, Mt. Baekunsan, elev. 835 m, 2 Sep 2013, Y. H. Cho & H. J. Na 20130902-010 (KB).

Key to species of Carpesium in Korea

  • 1. Radical leaves rosulate.

    • 2. Radical leaves oblanceolate; involucre subglobose ·············································· C. glossophyllum

    • 2. Radical leaves spatulate-lanceolate; involucre depressed-globose ······································· C. rosulatum

  • 1. Radical leaves withered before anthesis.

    • 3. Plants biennial; stems dichotomously forked ·························································· C. abratanoides

    • 3. Plants perennial; stems not forked.

      • 4. Involucre over 2 cm in diameter ······························································ C. macrocephalum

      • 4. Involucre less than 2 cm in diameter.

        • 5. Petiole distinctly winged.

          • 6. Involucre cupuliform, over 1 cm in diameter ·········································· C. cernuum

          • 6. Involucre cupuliform, less than 1 cm in diameter ·································· C. triste

        • 5. Petiole narrowly winged only in the upper part.

          • 7. Heads pedunculate; lower cauline leaves rounded to truncate ··········· C. divaricatum

          • 7. Heads sessile; lower cauline leaves cordate ························································· C. matsuei

NOTES

ACKNOWLEDGMENTS
We would like to express our sincere gratitude to KB and KH. This research was supported by a grant from the National Institute of Ecology (NIE), funded by the Ministry of Environment (MOE) of the Republic of Korea (NIE-A-2025-01).
CONFLICTS OF INTEREST
The authors declare that there are no conflicts of interest.

Fig. 1
Distribution of Carpesium matsuei. Distribution data in Japan based on Endemic Plants of Japan (Kato and Ebihara, 2011).
kjpt-56-2-165f1.jpg
Fig. 2
Major morphological characteristics of Carpesium matsuei. A. Habit. B. Whole plant. C. Basal leaf. D. Cauline leaf. E. Synflorescence. F. Capitulum (front view). G. Capitulum (side view). H. Longitudinal section of the capitulum. I. Stem. J. Tubular floret. K. Fruiting head. L. Achene.
kjpt-56-2-165f2.jpg
Table 1
Important morphological characters of Korean Carpesium.
Character C. abrotanoides C. cernuum C. divaricatum C. glossophyllum C. macrocephalum C. rosulatum C. triste C. matsuei
Stem
 Length (cm) 50–100 30–100 25–150 25–50 ca. 100 5–45 40–100 30–100
 Hair Upward pubescent Densely white villous Densely pubescent Densely pubescent Short pubescent Densely pubescent Dense1y pubescent Densely pubescent
Leaves
 Shape Broadly elliptic to oblong Spatulate to oblong Ovate to ovate-oblong Oblong, lanceolate Broadly ovate Spatulate, lanceolate Ovate to oblong Ovate to broadly ovate
 Apex Acute to obtuse Obtuse Acute to obtuse Acute, obtuse Acute Obtuse to rounded Acuminate Acute, acuminate
 Margin Mucronate-dentate Doubly serrate Mucronate dentate Entire Double toothed Sparsely mucronate toothed Mucronate toothed Mucronate toothed
 Base Narrowed Abruptly narrowed Rounded, cordate or truncate Cuneate Abruptly narrowed Oblanceolate Rounded Cordate
 Length (cm) 20–28 9–25 7–23 9–15 30–40 6–15 13–20 9–20
 Width (cm) 8–15 4–6 3–10 2.5–3.5 10–13 1.2–3 3–5 6–14
 Petiolate Broadly winged Winged Shortly winged - Winged - Winged Narrowly winged
Bract
 Shape Long oblong Linear-lanceolate Lanceolate Linear Linear-lanceolate Obovate Linear-lanceolate Lanceolate
Flowering season Sep to Nov Jul to Sep Aug to Oct Aug to Oct Aug to Oct Aug to Oct Aug to Oct Aug to Oct
 Head
  Type Axillary, branches Branches or axillary, nodding Terminal on branches Terminal branches, nodding Terminal, long peduncles Terminal Branches Axillary, sessile on each branch
  Shape Campanulate globose Cupuliform Ovoid Cupuliform Cupuliform Depressed globose Campanulate Ovoid to subglobose
  Length (mm) 7–10 7–8 6–8 5–8 8–10 6.5 5–6 5–6
  Diameter (mm) ca. 5 15–18 5–6 8–15 23–30 ca. 5 6–10 6–9
  Involucre
   Phyllaries 3 seriate 2 seriate 4 seriate 5 seriate 4 seriate 3 seriate 3 seriate 3–4 seriate
 Florets
  Corolla length (mm) 1.5 1.5 2.5 2.5 3.5 2.5 2.5 1.8–2
  Disc length (mm) 2.5 2.5 3–3.5 3.5 4 2.5 3.5 3–4
 Fruit
  Achene length (mm) 3.5 4.5–5 3.5 3.5–4 5.5–6 3.5 3–3.5 3.5

LITERATURE CITED

Cho, Y.-H. 1991. Karyotype analysis of eight species and one variety of Carpesium (Compositae) in Japan. Journal of Japanese Botany 66: 26-34.

Gupta, R. C., Kataria, V. and Mehra, A. 2012. Cytomorphological studies in some gamopetalous species of Western the Himalaya: An attempt to add new or varied cytotypes. Chromosome Botany 7: 59-65.
crossref
Iwatsuki, K., Yamazaki, T. Boufford, D. E. and Ohba, H. 1995. Flora of Japan. IIIb: Kodansha, Tokyo. Pp. 98-100.

Kato, M. and Ebihara, A. 2011. Endemic Plants of Japan. Tokai University Press, Kanagawa. Pp. 151-152.

Kim, K.-J. 2020. Genus Carpesium. Flora of Korea. 6c-2: Park, J. W. (ed.), National Institute of Biological Resources, Incheon. Pp. 12-15.

Kitamura, S. 1936. Compositae novae Japonicae X. Acta Phytotaxonomica et Geobotanica 5: 27-28.

Kitamura, S. 1957. Carpesium . Memoirs of the College of Science, University of Kyoto, Series B,, 24: Pp. 48 pp.

Nishikawa, T. 1984. Chromosome counts of flowering plants of Hokkaido (7). Journal of Hokkaido University of Education, Section 2B. 35: Pp. 31-42.

Ohashi, H., Kadota, Y. Murata, J. Yonekura, K. and Kihara, H. 2017. Wild Flowers of Japan. Heibonsha, Tokyo. Pp. 351-353.

Ohwi, J. 1965. Carpesium L. Flora of Japan. Smithsonian Institution, Washington, D.C. Pp. 861-863.

Xu, B. S., Weng, R. F. and Zhang, M. Z. 1992. Chromosome numbers of Shanghai plants I. Investigatio et Studium Naturae 12: 48-65.

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