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In a preliminary experiment, the chromosome number of 2n = 36 was observed in C. matsuei (a Korean population, unpublished data).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).








