Bupleurum baimaense (Apiaceae), a new species from Hengduan Mountains, China

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Ann. Bot. Fennici 50: 379 385 ISSN 0003-3847 (print) ISSN 1797-2442 (online) Helsinki 10 October 2013 Finnish Zoological and Botanical Publishing Board 2013 Bupleurum baimaense (Apiaceae), a new species from Hengduan Mountains, China Xiang-Guang Ma, Cai Zhao, Qian-Long Liang & Xing-Jin He* Key Laboratory of Bio-Resources and Eco-Environment of Ministry of Education, College of Life Science, Sichuan University, Wangjiang Road 29, Chengdu 610064, China (*corresponding author s email: xjhe@scu.edu.cn) Received 4 Apr. 2013, final version received 20 June 2013, accepted 28 June 2013 Ma, X. G., Zhao, C., Liang, Q. L. & He, X. J. 2013: Bupleurum baimaense (Apiaceae), a new species from Hengduan Mountains, China. Ann. Bot. Fennici 50: 379 385. Bupleurum baimaense X.G. Ma & X.J. He sp. nova (Apiaceae) is proposed here based on morphological characters and chromosome number (2n = 12). The material of this species has thus far been treated in China as B. dalhousieanum. However, B. baimaense has no branches or lateral umbels on stems, whereas B. dalhousieanum has branches and lateral umbels on the distal part of stems. Bupleurum baimaense is most similar to B. commelynoideum, but differs mainly by its stems usually being decumbent and numerous. Bupleurum baimaense is known from northwest Yunnan (Deqin) and southeast Tibet (Zayul) in China. Bupleurum (Apiaceae) is a genus of about 180 species (Sheh & Watson 2005). The taxonomy of the genus is extremely difficult on account of obscure inter-specific boundaries and wide intraspecific morphological variation. After the publication of the accounts of Bupleurum in Flora Reipublicae Popularis Sinicae (Li & Sheh 1979) and Flora of China (Sheh & Watson 2005), additional taxonomic changes have been proposed for the Chinese taxa of Bupleurum (e.g. Wang et al. 2011a, 2011b). Despite the former achievements, which include many taxonomic rank adjustments and proposals of new species and new combinations, the species limits are not yet well resolved in some taxa. Shan and Li (1974) first identified some Bupleurum specimens from Deqin County of the Yunnan province as B. dalhousieanum (T. T. Yu 9312, KUN). Li and Sheh (1979) and Sheh and Watson (2005) subsequently agreed that those plants indeed represented B. dalhousieanum and extended the distribution of this species to include the Hengduan Mountain region in China. During our field investigations in 2010 2012, we collected Bupleurum plants and fruits from the Bai-ma Mountain (Deqin County, southwestern China) from the same site where the specimens identified as B. dalhousieanum by Shan and Li (1974) came from. We also collected some specimens with the same appearance as the specimens from Deqin at Zayul in Tibet. By comparing the Deqin and Zayul specimens with the syntypes of B. dalhousieanum in the Kew herbarium (C. B. Clarke 22151, 22679, 22987B, 23260 (Fig. 1), 23957), we found that the species we collected was not B. dalhousieanum. Both species are branched at base and usually have procumbent stems, but their branching patterns are quite different. Bupleurum dalhousieanum has branches and lateral umbels on the

380 Ma et al. Ann. BOT. Fennici Vol. 50 Fig. 1. A syntype of Bupleu r um dalhousieanum (C. B. Clarke 23260, K). Image published with permission from The Royal Botanic Gardens KEW. distal part of the stems. However, the species we collected from Deqin and Zayul lacks branches and lateral umbels on the flowering stems. Furthermore, according to Clarke s (1879: 677) description of var. dalhousieana, it has yellow petals, while those of the species we collected from Deqin and Zayul are purple. Moreover, the taxa we collected can be distinguished from B. dalhousieanum by the size of the bracteoles: B. dalhousieanum has bracteoles shorter than or equal to the length of fruits, while the taxon we focus herein usually has bracteoles prominently exceeding fruits in length (Figs. 2D and 3B). To study the chromosome number of the species, we collected mature fruits of the Bai-ma Mountain population in October 2012. The root

Ann. BOT. Fennici Vol. 50 Bupleurum baimaense, a new species from China 381 Fig. 2. A: Habitat of Bupleurum baimaense (Bai-ma Mountain, Yunnan, China). B: B. baimaense in flower. C: B. baimaense in fruit. D: Inflorescence and fruits of B. baimaense. E: Fruits of B. baimaense. F: Transverse section of fruit of B. baimaense. tips from the germinated plants were pretreated in saturated para-dichlorobenzene solution for 5 7 h at room temperature. Then they were fixed in a solution of ethanol: acetic acid (3:1) for at least 12 h at 4. Fixed roots were hydrolysed in 1 mol l 1 HCl at 58 for 6 8 min and then stained with modified carbol fuchsin (Kao 1982) for 15 20 min. For chromosome number counting, photographs were taken with an Olympus BX51 microscope. Cytological analysis revealed that the chromosome number is 2n = 12 (x = 6) (Fig. 4), i.e. different from B. dalhousieanum, reported as 2n = 16 (x = 8) (Pimenov et al. 2001). Based on these differences, we propose that the specimens described as B. dalhousieanum from Deqin in 1974 are placed in the species described here. Bupleurum baimaense X.G. Ma & X.J. He, sp. nova (Figs. 2 and 3) B. dalhousieanum auct. non (C.B. Clarke) Koso-Pol. (e.g. Shan & Li 1974, Li & Sheh 1979, Sheh 1986, Sheh 1997, Sheh & Watson 2005). Holotype: China. Yunnan province, Deqin County, Bai-ma Mountain, screes, alt. 4400 m, 19 Oct. 2012, X.

382 Ma et al. Ann. BOT. Fennici Vol. 50 Fig. 3. Holotype of Bupleurum baimaense. A: Fruiting specimen. B: Inflorescence and young fruits. G. Ma m12101901 (SZ), in fruit. Paratypes: China. Yunnan province, Deqin County, Bai-ma Mountain, screes, alt. 4400 m, 18 Aug. 1981, Hengduan Expedition of IB 3236 (PE), and 8 Jul. 2011, B. Xu 558 (KUN); Yunnan, Deqin, Bai-ma Mountain, Chialoti, 30 July 1937, T. T. Yu 9312 (KUN); Tibet, Zayul, Ridong village, 3800 m, gravel slope, 17 Aug. 2011, X. G. Ma XZ2011081737 (SZ); Tibet, Zayul, Ridong village, scrub, grasslands, 3800 m, 20 Sep. 1982, Qinghai-Tibet Expedition 10583 (PE). Etymology: The specific epithet is derived from the type locality: Bai-ma Mountain, Deqin County, Yunnan. Plants (5 )10 35 cm, perennial. Rootstock slender, woody, branched. Stems purplish-red, numerous, usually decumbent, base without fibrous remnant sheaths, not branched above. Basal leaves usually numerous; blade linear to linear-lanceolate, 3 10 0.2 0.4 cm, 5 7nerved, gradually tapering into petiole. Upper leaves sessile; blade lanceolate to ovate, 1.5 5 0.3 1 cm, base rounded, clasping, apex acuminate, sometimes caudate. Umbels terminal; rays 2 4, 1 5 cm, unequal; bracts 1 3, ovate, 5 23 4 8 mm, unequal; bracteoles (4 )6 10, broadly ovate or obovate, tinged purple, 4 8 3.5 6 mm, exceeding flowers and fruits; umbellules 8 17 mm across, 16 24-flowered; pedicels 1 2 mm; Petals purplish, sometimes margins yellow; Stylopodium low-conic, dark purple. Fruit oblong-ovoid, ca. 4 2 mm; ribs narrowly

Ann. BOT. Fennici Vol. 50 Bupleurum baimaense, a new species from China winged; vittae 3 in each furrow, 4 on commissure; fruit wall swollen when ripe. Flowering and fruiting July October. Habitat: On alpine screes or gravel slopes, at elevations over 3800 m a.s.l. As described above, B. dalhousieanum is morphologically distinct from B. baimaense. The type locality of B. dalhousieanum is Dalhousie and Dhurmsala in N India. The distribution range of this species includes N India, Nepal and W Tibet of China. Bupleurum baimaense is distributed in NW Yunnan (Deqin) and SE Tibet (Zayul). Bupleurum baimaense can be distinguished from the other procumbent W Himalayan alpine members of Bupleurum, such as B. atroviolaceum and B. gracillimum, by its unbranched stems and longer bracteoles. In Wang et al. (2011b), we identified a specimen from Muli, Sichuan (X. G. Ma m10093013, SZ) as B. dalhousieanum (Fig. 5). However, that was a misidentification. This as yet unrecognized species is similar to B. baimaense, but shorter (5 15 cm) and with fewer rays (1 2, usually 1). The taxonomic position of that specimen has not been assigned at present because of lack of mature fruits and chromosome data. With the exception of that unrecognized species, B. baimaense is most similar to B. commelynoideum, which is common in W Sichuan. Although B. baimaense and B. commelynoideum share some Fig. 5. The specimen (X. G. Ma m10093013, SZ) collected from Muli, Sichuan, China (see text). 383 Fig. 4. Metaphase chromosomes of Bupleurum baimaense (from the holotype). similarities, it is easy to distinguish them. A comparison of B. baimaense, B. dalhousieanum, B. commelynoideum, B. atroviolaceum and B. gracillimum is presented in Table 1. Additional specimens examined: Bupleurum dalhousieanum. India. Himachal Pradesh, 11 Sep. 1874, C. B. Clarke 22151 (K), C. B. Clarke 22679 & 22987B (K); 29 Sept. 1874, C. B. Clarke 23260 (K); 17 Oct. 1874 C. B. Clarke 23957

384 Ma et al. Ann. BOT. Fennici Vol. 50 Table 1. Comparison of morphological characters and geographic distribution of Bupleurum baimaense, B. dalhousieanum, B. atroviolaceum, B. gracillimum and B. commelynoideum. Characters B. baimaense B. dalhousieanum B. atroviolaceum B. gracillimum B. commelynoideum Number of flowering stems numerous numerous numerous numerous usually less than per plant three Flowering stems position usually decumbent usually decumbent decumbent decumbent usually erect Stem branching pattern unbranched above branched above branched above branched above occasionally branched above Ray number 2 4 3 5 2 4 2 5 3 7 Bract number 1 3 1 3 2 3 2 5 0 2 Bracteole relative exceeding fruits shorter than or shorter than or shorter than or exceeding fruits length equal to fruits equal to fruits equal to fruits Petal color purple, margin usually yellow dark purple to black usually yellow adaxially purple or sometimes yellow yellowish-tinged, abaxially purple Distribution Hengduan mountains N India, Nepal N India, Afghanistan W Himalayas W Sichuan and (Deqin and Zayul) and W Tibet and Pakistan NE Yunnan (K). China. Tibet, Nyalam, 3710 m, 1 July 1966, Y. T. Zhang et al. 4619 (PE); Nyalam, 3810 m, 22 June 1975, C. Y. Wu et al. 75-451 (PE); Nyalam, 3800 m, 23 June 1975, Qinghai- Tibet Expedition 5821 (PE); Gyirong, 4300 m, 28 July 1975, Qinghai-Tibet Expedition 5620 (PE); Burang, 4400 m, 14 July 1976, Qinghai-Tibet Expedition 76-8436 (PE). Bupleurum atroviolaceum. India. Jammu-Kashmir, 28 Aug. 1928, R. R. Stewart 9880 (K). Afghanistan. Badakhshan, east shore of Lake Shewa, 3195 m, 28 June 2008, M. Jacobs & C. Schloeder 1706 (KUFS); Parwan, Salang-Suedeite, 3600 m, 8 Aug. 1969, S. Breckle 2673 (KUFS). Bupleurum gracillimum. Afghanistan. Badakhshan, 15 July 1971, O. Anders 7457 (KUFS). Bupleurum commelynoideum. China. Sichuan, Muli, 17 June 1982, Q. S. Zhao et al. 8474 (CDBI). Sichuan, Xiangcheng, 3 Aug. 1981, Qinghai-Tibet Expedition 3686 (CDBI). Sichuan, Kangding, 21 Sep. 1998, M. G. Pimenov et al. 291 (PE). Acknowledgements We thank Dr. Bo Xu of the Kunming Institute of Botany, Chinese Academy of Sciences for providing photos of living plants in the flowering season. We appreciate the assistance of the staff in the herbaria of K, PE, KUN, CDBI, SZ and WU in the study of specimens. This research was supported by the National Natural Science Foundation of China (grant nos. 31070166, 31100161, 31270241), and the specimen platform of China and teaching specimen s sub-platform (http://mnh.scu.edu.cn/). We are grateful to Dr. Xian-Qin Wei and Dr. Yun-Dong Gao for improving the English. We also appreciate the contribution of reviewers and journal editor, and the permission obtained from the Kew herbarium to print the image of a type specimen. References Clarke, C. B. 1879: Bupleurum L. In: Hooker, J. D. (ed.), The Flora of British India, vol. 2: 677. L. Reeve & Co., London. Kao, K. N. 1982: Staining methods for protoplasts and cells. In: Wetter, L. R. & Constabel, F. (eds.), Plant tissue culture methods: 67 71. National Research Council of Canada, Saskatoon. Li, Y. & Sheh, M. L. 1979: Bupleurum L. In: Shan, R. H. & Sheh, M. L. (eds.), Flora Reipublicae Popularis Sinicae, vol. 55: 215 295. Science Press, Beijing. [In Pimenov, M. G., Alexeeva, T. V. & Kljuykov, E. V. 2001: IOPB chromosome data 17. Newslett. Int. Organ. Pl. Biosyst. Průhonice 33: 24 25. Shan, R. H. & Li, Y. 1974: On the Chinese species of Bupleurum L. Acta Phytotax. Sinica 12: 261 294. [In Sheh, M. L. 1986: Bupleurum L. In: Wu, Z. Y. (ed.), Flora Xizangica, vol. 3: 445 459. Science Press, Beijing. [In

Ann. BOT. Fennici Vol. 50 Bupleurum baimaense, a new species from China 385 Sheh, M. L. 1997: Bupleurum L. In: Wu, Z. Y. (ed.), Flora Yunnanica, vol. 7: 455 472. Science Press, Beijing. [In Sheh, M. L. & Watson, M. F. 2005: Bupleurum L. In: Wu, Z. Y., Raven, P. H. & Hong, D. Y. (eds.), Flora of China, vol. 14: 60 74. Science Press, Beijing; and Missouri Botanical Garden Press, St. Louis. Wang, C. B., Ma, X. G. & He, X. J. 2011a: Bupleurum candollei var. paucefulcrans comb. nov. (Apiaceae) from Guizhou, China: comparison of allied species based on morphology, anatomy and molecular data. Nordic Journal of Botany 29: 424 430. Wang, C. B., Ma, X. G. & He, X. J. 2011b: A taxonomic re-assessment in the Chinese Bupleurum (Apiaceae): Insights from morphology, nuclear ribosomal internal transcribed spacer, and chloroplast (trnh-psba, matk) sequences. Journal of Systematics and Evolution 49: 558 589. This article is also available in pdf format at http://www.annbot.net