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Viola kwangtungensis Melch. (Violaceae): a New Record Viola in Taiwan

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Viola kwangtungensis Melch. (Violaceae):

a New Record Viola in Taiwan

Chang-Tse Lu,

1)

Yu-Long Hung,

2)

Chih-Hsiung Chen

3,4)

【 Summary】

In this paper, a new record Viola species of Taiwan, V. kwangtungensis Melch., is reported.

This newly recorded species was found at elevations of 1300~1600 m in Taiwan, growing in shady soil on a slope under a bamboo plantation. It is similar to V. mucronulifera Handel-Mazzetti and V. formosana Hayata var. kawakamii (Hayata) Chen & Yang, as well as V. adenothrix Hayata var.

adenothrix and V. nagasawae Makino & Hayata var. pricei (W. Becker) Wang & Huang. Detailed differences in diagnostic morphological features of these species are discussed in this paper.

Key words: new record species, Taiwan, Violaceae, Viola kwangtungensis.

Lu CT, Hung YL, Chen CH. 2019. Viola kwangtungensis Melch. (Violaceae): a new record Viola in Taiwan. Taiwan J For Sci 34(2):135-42.

1) Department of Biological Resources, National Chiayi University, 300 Syuefu Rd., Chiayi 60004, Taiwan. 國立嘉義大學生物資源學系,60004嘉義市鹿寮里學府路300號。

2) Amateur nature observer, 188 Jincheng Street, Jindun Village, Huatan Township, Changhua 50343, Taiwan. 生態攝影家,50343彰化縣花壇鎮金墩村金城街188號。

3) Department of Biology, National Museum of Natural Science, 1 Guancian Rd., Taichung 40453, Taiwan. 國立自然科學博物館生物學組,40453台中市館前路1號。

4)Corresponding author, e-mail:alanchen@mail.nmns.edu.tw 通訊作者。

Received September 2018, Accepted May 2019. 2018年9月送審 2019年5月通過。

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研究簡報

台灣堇菜科的新紀錄種—廣東堇菜

呂長澤

1)

洪裕榮

2)

陳志雄

3,4)

摘 要

為本文報導了台灣一新記錄種的堇菜-廣東堇菜 (Viola kwangtungensis Melch.)。這種新的

記錄物種分布於台灣海拔1300~1600 m山區,生長在竹林下的斜坡上。它近似於小尖堇菜 (V.

mucronulifera Handel-Mazzetti) 和川上氏堇菜 (V. formosana Hayata var. kawakamii (Hayata) Chen

& Yang) , 以及喜岩菫菜 (V. adenothrix Hayata var. adenothrix) 與普萊氏菫菜 (V. nagasawae Makino &

Hayata var. pricei (W. Becker) Wang & Huang)。在本文中,我們對這些物種在形態特徵上的詳細差 異進行討論。

關鍵詞:新紀錄種、台灣、堇菜科、廣東堇菜。

呂長澤、洪裕榮、陳志雄。2019。台灣堇菜科的新紀錄種—廣東堇菜。台灣林業科學34(2):135-42。

Viola Linnaeus (1753: 933) comprises approximately 600 species worldwide (Mar- cussen et al. 2015) and is the largest genus of the Violaceae (Wahlert et al. 2014). It is monophyletic and is thought to have diversi- fied ca. 30 Mya in South America (Ballard et al. 1999). Viola consists of at least 17 mono- phyletic lineages and putative sections (Fan et al. 2015) and is currently undergoing revi- sion (Marcussen et al. 2015). In East Asia, the genus is mostly distributed in temperate regions, and numerous new species have been described in recent years [such as V. austrosi- nensis (Chen and Yang 2008), V. maoersha- nensis, V. nitida (Chen and Yang 2009), V.

changii (Zhou and Xing 2007), V. nanlingen- sis (Zou et al. 2008), V. guangzhouensis (Dong et al. 2009), and V. jinggangshanensis (Ning et al. 2012)]. In total, 16~18 Viola species have been reported to occur in Taiwan (Wang and Huang 1990, 1993, Wang 1991, Yang et al. 2000, Chen et al. 2007).

Recently, according to our botanical fieldwork in central Taiwan, an unfamiliar

species of Viola was found by the second and third authors. This species was always found growing in shady soil on slopes under a bam- boo plantation. Taking into consideration the characteristics of the slender, elongated sto- lons with scattered leaves, rootlets emitting from nodes and internodes of stolons, and the acute apex of the lower petal, this unfamiliar species should belong to the Viola series Aus- tralasiaticae Okamoto (Okamoto et al. 1993).

Subsequent observations and a litera- ture survey were carried out. Eventually we confirmed this species to be V. kwangtun- gensis Melch., a species endemic to China (Chen et al. 2007). And now we report it as a newly recorded species in Taiwan.

Diagnostic morphological characteristics

of this new record species were compared

to those of congeners found in Taiwan and

neighboring areas, and are summarized in a

table. Additionally, distribution maps, and

a discussion of this new record species and

similar taxa in Taiwan and neighboring ar-

eas are provided.

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Taxonomic description

Viola kwangtungensis Melch. Sunyatsenia 1:124. 1933. ... 廣東堇菜 (Figs. 1, 2)

Type: CHINA. Prov. Kwangtung: Lung Tou Shan, Kook Kiang, on slope, fl. 7 Apr.

1930, S.P. Ko 50326 (isotype A, photo!).

Perennial herb. Rhizome long, slender, 2~7 cm long; internodes remote. Stolon up to 15 cm, slender, glabrous, rootlets emitting from nodes

and internodes of stolons, top developing into a new plant. Leaves nearly basal or clustered on shortened stem; stipules adnate to petioles only at base, brown or greenish with dark striations, free part lanceolate, ca. 10×1.5 mm, margin short-fimbriate, apex acuminate; petioles sub- equal blades, 3.5~7.5 cm, glabrous; leaf blade ovate to ovate-triangular, 2~4.5×1.5~3 cm, adaxially deep-green, midvein conspicuously

Fig. 1. Viola kwangtungensis. A, Habit; B, stipules; C, inflorescence; D, flower (front view);

E, petals; F, stamens; G, stamen with nectariferous appendage; H, pistil; I, dehiscent

capsule; J, seeds. Drawing based on C.-H. Chen 10831 (TNM!).

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Fig. 2. Viola kwangtungensis. A, Habit; B, live plants with a long stolon; C, stipules; D,

flower (lateral view), showing saccate spur; E, bisection of flower, showing stamens and

nectariferous appendage; F, dehiscence capsule; G, bisection of flower, showing pistil and

ovules.

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raised, glabrous, abaxially grayish-green, usually purplish-red along veins, base cordate, margin crenate, 7~12-toothed on each side, teeth sub- orbicular, not spinose at apices. Flowers white or light-purplish; pedicels usually exceeding leaves, glabrous, 2-bracteolate above middle;

bracteoles linear-triangular, ca. 6 mm. Sepals purplish-red, lanceolate, 3~5×1~1.2 mm, sparsely pubescent, basal auricles short, < 1 mm, apex truncate, sparsely shallowly dentate. Petals oblong-obovate, upper ones subequal to lateral ones, 9~10×4~5 mm, lateral ones glabrous, 8~9×4~4.5 mm, anterior one shorter, 7~8×3 mm (spur included), distinctly violet striped, apex acute; spur saccate, short, 3~4 mm, stout, ca. 2 mm in diameter; nectariferous appendages of 2 anterior stamens, acutangular, ca. 2 mm, subequal to anthers. Ovary oblong-globose, glabrous; styles clavate, base slightly geniculate, gradually thickened upward; stigmas slightly raised at apex, thickened and narrowly margined on lateral sides, inconspicuously beaked at apex, with a small stigma hole open upward at tip of beak. Capsule ellipsoid, 6~9.5 mm long, gla- brous. Seeds ca. 0.9 mm long.

Specimens examined: TAIWAN. Nan- tou County: Luku Township, elev. 1600 m, 31 May 2011, Chen C.-H., C.-M. Wang, &

Y.-J. Hung 10556 (TNM); Chushan Town, Shanlinhsi, elev. 1350~1450 m, 29 May 2013, Chen C.-H. 11099 (TNM). Chiayi County:

Arisan [Alishan], inter Funkiko et Toroyen, 20 Jan. 1912, Hayata & Sasaki s.n. (TAIF, identified as V. kawakamii Hayata); Chuchi Township, Chuchi, elev. 1400~1500 m, 4 May 2011, Chen C.-H., C.-M. Wang, & Y.-J.

Hung 10544 (TNM).

Distribution and habitat: Viola kwang- tungensis is distributed in China and Taiwan.

In China, its distribution is restricted to Fujian, N. Guangdong, Hunan, Jiangxi, and Sichuan Provinces (Chen et al. 2007, Chen and Yang 2008). So far, it is only known from 2 small

areas, Shanlinhsi, Nantou County and Funchi- hu, Chiayi County, in Taiwan (Fig. 3). It was found there along a trail, growing in shady soil on a slope under bamboo plantations, at eleva- tions of 1300~1600 m. This area is situated in the montane zone with a humid microclimate due to being located in a cloud forest area. Its flowering period is from March to early May and fruiting period is from late March.

Discussion: Compared to other species in the Viola series Australasiaticae, V. kwang- tungensis is closely related to V. mucronu- lifera Handel-Mazzetti. Viola kwangtungensis resembles V. mucronulifera, which both share the characteristic of a leaf margin that is spinose at the apices of teeth. However, in V. kwangtungensis the apices of the teeth are spinose, but in V. mucronulifera in between teeth is spinose (Fig. 4).

In Taiwan, V. kwangtungensis occurs sympatrically with V. formosana Hayata var.

kawakamii (Hayata) Chen & Yang. These 2 species share glabrous leaves and similar vegetative bodies. If they are not flowering, it is difficult to distinguish them. Because of their similar habitats and vegetative bodies, V.

kwangtungensis has been misidentified as V.

formosana var. kawakamii; e.g., a specimen of V. kwangtungensis (e.g., Hayata & Sasaki s.n. collected from Alishan) was previously misidentified as V. kawakamii (= V. formosana var. kawakamii). However, V. kwangtungensis can be easily distinguished from V. formosana var. kawakamii by the following characteris- tics: leaf apex (obtuse vs. acute), the anterior petal (shortest, acute at the apex vs. longest, deeply emarginate or shallowly 2-lobed), spur (short, saccate, 3~4 mm vs. longer, cy- lindrical, 5~7 mm, slightly curved), and leaf margin (shortly spinose at apices of teeth vs.

absent). Additionally, V. kwangtungensis also

resembles V. adenothrix Hayata var. adeno-

thrix and V. nagasawae Makino & Hayata var.

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Fig. 3. Distribution map of Viola kwangtungensis in Taiwan. Each star represents a distribution location.

Fig. 4. Leaf margin comparison of Viola kwangtungensis and V. mucronulifera. A. Viola kwangtungensis (Taiwan) from C.-H. Chen 10831; B, V. kwangtungensis (China) from isotype S.P. Ko 50326; C, V. mucronulifera from isotype R.C. Ching 7016. Arrows indicate the spinose feature at the leaf margin.

pricei (W. Becker) Wang & Huang, because they grow in similar habitats. However, the former can be distinguished from the latter two by leaf texture (glabrous vs. hirsute) and leaf shapes (ovate to ovate-triangular vs. el- liptical to elliptical-ovate or ovate-cordate,

and triangular-ovate to lanceolate). A detailed comparison of V. kwangtungensis with V. ad- enothrix var. adenothrix, V. formosana var.

kawakamii, V. nagasawae var. pricei and V.

mucronulifera is provided in Table 1.

Although we regarded this taxa as V.

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Table 1. Morphological comparison of V iola kwangtungensis with V. adenothrix var . adenothrix , V . formosana var . kawakamii , V. nagasawai var . pricei , and V. mucronulifera

V. kwangtungensisV. kwangtungensis1) V. adenothrixV. formosanaV. nagasawaiV. mucronulifera2) (population in Taiwan)(China)var. adenothrix3)var. kawakamiivar. pricei Stipulesmargin sparselymargin long-fimbriatemargin fimbriate ormargin fimbriatemargin sparselymargin long short-fimbriatelaciniateor erosefimbriate-laciniatefimbriate-dentate Leaf ovate to ovate-triangular, orbicular or sometimeselliptical to elliptical-broadly triangular- triangular-ovateovate-cordate blade2~4.5×1.5~3 cmreniform, 1~3×1~3 cmovate or ovate-cordate,cordate,to lanceolate,or elliptic-cordate, 1~5×1~4 cm1.5~4×1~4 cm1~3×1~2.5 cm2~5×1.5~3 cm Leafcrenate, inconspicuouslydeeply mucronate-shallowly crenatecrenate, teeth notcrenate on margin,crenate, teeth subor- marginshortly spinose in teethcrenate, shortlyon margin, subdentatespinoseteeth not spinosebicular, conspicuously spinose in teethon lobes, teeth notspinose at apices, spinosespines spreading or bending forward Leafcordateplane cordatecordate with cordatebroadly cordatenarrowly cordate baserounded basal lobes Sepalsparsely pubescent,usually pubescent,sparsely pubescent,narrowly lanceolate,sparsely ciliate toglabrous, ca. 5×1~1.2 3~5×1~1.2 mm;3~5×1.5~2 mm;3~7×1~1.5 mm;3~5×0.5~1.5 mmalmost entire onmm; basal auricles short basal auricles short,basal auricles absentbasal auricles margin, 5~8×1~1.5 < 1 mmca. 0.5 mmmm; basal auricles up to 0.5 mm Anterior7~8×3 mm,ca. 9 mm, apex acuteapex emarginate;ca. 15 mm, apexapex acute;ca. 11×ca. 3 mm, petal (spur apex acutespurs 0.8~2 mm longdeeply emarginate spurs 1~1.5 mm longapex acute included)or shallowly 2- lobed 1) Description based on Melchior (1933) and Chen et al. (2007); 2) Description based on Chen et al. (2007); 3) Description based on Wang and Huang (1993).

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kwangtungensis, individuals in Taiwan also slightly differ from individuals in China. For example, the leaf shape is ovate to ovate-trian- gular, base cordate, and leaf margin inconspic- uously shortly spinose in teeth in the former, while the leaf shape is orbicular or sometimes reniform, base plane is cordate, and the leaf margin is obviously shortly spinose in teeth in the latter (Fig. 4). We consider that further study is required to elucidate their relationship.

ACKNOWLEDGEMENTS

The authors are grateful to the curators of various herbaria (HAST, TAI, TAIF, TI, and TNM) for access to the herbarium collec- tions or loan of type specimens, and the artist Hsueh-Hua Yang for the illustrations.

LITERATURE CITED

Ballard HE, Sytsma KJ, Kowal RR. 1999.

Shrinking the violets: phylogenetic relation- ships of infrageneric groups in Viola (Violace- ae) based on internal transcribed spacer DNA sequences. Syst Bot 23:439-58.

Chen YS, Yang QE. 2008. A new species of Viola (Violaceae) from southern China. Bot J Linn Soc 158:755-61.

Chen YS, Yang QE. 2009. Two new stolonif- erous species of Viola (Violaceae) from China.

Bot J Linn Soc 159:349-56.

Chen YS, Yang QE, Ohba H, Nikitin VV.

2007. Violaceae. In: Wu ZY, Raven PH, edi- tors. Flora of China 13:72-111. Beijing: Sci- ence Press; St. Louis, MO: Missouri Botanical Garden Press.

Dong AQ, Zhou JS, Gong Q, Xing FX.

2009. A new species of Viola (Violaceae) from Guangdong, China. Novon 19:457-60.

Fan Q, Chen S, Wang L, Chen Z, Liao W.

2015. A new species and new section of Viola (Violaceae) from Guangdong, China. Phyto-

taxa 197:15-26.

Marcussen T, Heier L, Brysting AK, Oxel- man B, Jakobsen KS. 2015. From gene trees to a dated allopolyploid network: insights from the angiosperm genus Viola (Violaceae). Syst Biol 64:84-101.

Melchior H. 1933. Viola kwangtungensis, a new Violet from China. Sunyatsenia 1:124-7.

Ning ZL, Zeng ZX, Chen L, Xu BQ, Liao JP. 2012. Viola jinggangshanensis (Violaceae), a new species from Jiangxi, China. Ann Bot Fenn 49:383-6.

Okamoto M, Okada H, Ueda K. 1993. Mor- phology and chromosome number of Viola pilosa, and its systematic position. Taxon 42:781-7.

Wahlert GA, Marcussen T, de Paula-Souza J, Feng M, Ballard HE. 2014. A phylogeny of the Violaceae (Malpighiales) inferred from plastid DNA sequences: implications for ge- neric diversity and intrafamilial taxonomy.

Syst Bot 39:239-52.

Wang QR. 1991. Violaceae. In: Wang QR, ed- itor. Flora Reipublicae Popularis Sinicae 51:1- 148. Beijing: Science Press.

Wang JC, Huang TC. 1990. Notes on the Flora of Taiwan (9) —The Viola L. (Violaceae).

Taiwania 35:12-56.

Wang JC, Huang TC. 1993. Viola L. In:

Huang TC et al. editors. Flora of Taiwan, 2nd ed. 3:807-34. Taipei, Taiwan: Editorial Com- mittee, Department of Botany, National Tai- wan Univ.

Yang YP, Liu HY, Lu SY. 2000. Manual of Taiwan vascular plants 3: 221-25. Taipei, Tai- wan: Council of Agriculture, Executive Yuan.

Zhou JS, Gong Q, Xing FW. 2008. Viola nanlingensis (Violaceae), a new species from Guangdong, southern China. Ann Bot Fenn 45:233-6.

Zhou JS, Xing FW. 2007. Viola changii sp.

nov. (Violaceae) from Guangdong, southern

China. Nord J Bot 25:303-5.

數據

Fig. 1. Viola kwangtungensis. A, Habit; B, stipules; C, inflorescence; D, flower (front view);
Fig. 2. Viola kwangtungensis. A, Habit; B, live plants with a long stolon; C, stipules; D,  flower (lateral view), showing saccate spur; E, bisection of flower, showing stamens and  nectariferous appendage; F, dehiscence capsule; G, bisection of flower, sh
Fig. 3. Distribution map of Viola kwangtungensis in Taiwan. Each star represents a  distribution location.
Table 1. Morphological comparison of Viola kwangtungensis with V. adenothrix var. adenothrix, V

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