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Research Article
A new species of Argyreia (Convolvulaceae) from Yunnan, China
expand article infoMao-Lin Zhang, Yi He, Quan-Ru Liu
‡ Beijing Normal University, Beijing, China
Open Access

Abstract

Argyreia subrotunda, a new species from Yunnan Province, China, is described and illustrated. The new species resembles A. fulvocymosa and A. wallichii, but differs from these in the flowers with an entire or shallowly lobed corolla, as well as smaller elliptic bracts, lax flat-topped cymes and shorter corolla tubes. An updated key to the species of Argyreia from Yunnan province is also provided.

Keywords

Argyreia subrotunda, flora of Yunnan, morphology, new taxon, taxonomy

Introduction

Argyreia Lour., a genus comprising scandent shrubs or lianas, is mainly distributed throughout tropical Asia (Staples and Traiperm 2017). Argyreia species mainly inhabit open and sunny places such as roadsides, thickets, and edges of mingled forest (Fang and Huang 1979; Fang and Staples 1995). The number of Argyreia species has been increasing and is now up to 143 species following the discovery of new species (Traiperm et al. 2019; Traiperm and Suddee 2020) and the establishment of new combinations (Shalini et al. 2017; Staples and Traiperm 2017; Rattanakrajang et al. 2022). There are about 25 species in China (14 of which are endemic) and 92% of the species found in China in Yunnan Province (23 recorded species). The province of Yunnan is, therefore, the main center of diversity in China (Fang and Huang 1979; Fang and Staples 1995; Yang et al. 2015).

Loureiro (1790) published Argyreia as a genus within Convolvulaceae. The genus is mainly characterized by indehiscent fleshy or mealy berries (Staples and Traiperm 2017). The various types of indumentum, inflorescence architecture, depth of corolla lobes, and number of seeds in individual berries are the main taxonomically informative characters for the delimitation of species in Argyreia.

Argyreia seems to be non-monophyletic in recent works, because it includes at least one of the moth-pollinated species of Rivea Choisy (Manos et al. 2001; Stefanovic et al. 2003). Furthermore, there is evidence that Blinkworthia Choisy should be subsumed under Argyreia (Rattanakrajang et al. 2022). We support this conclusion and although the Argyreia alliance clade as recovered is paraphyletic, only one Rivea species was used and the inclusion of other species might lead to different conclusions in the future (Rattanakrajang et al. 2022). Therefore, we think that Rivea and Argyreia are two independent genera and both supposedly monophyletic, but their limits should be revised under a phylogenetic perspective with a comprehensive sampling.

Although recent studies have shown that Argyreia should be treated as part of Ipomoea L. (Muñoz-Rodríguez et al. 2019) and Argyreia is merged into Ipomoea by Wood et al. (2020), we chose not to follow the proposed classification in the present work, as further study of Old World taxa is still required (Traiperm and Suddee 2020). As it concerns Ipomoea, the possibility to keep the several established smaller genera has the potential to maintain nomenclatural stability (Eserman et al. 2020). So we do not subsume Argyreia into Ipomoea at this time and accordingly maintain the well-established generic concepts (Rattanakrajang et al. 2022).

During recent field surveys in Yunnan Province, an interesting population of Argyreia with an entire or shallowly lobed corolla was found. After reviewing literature and comparing specimens, especially native species in Yunnan Province and adjacent countries (Vietnam, Laos, Myanmar, Cambodia and Thailand), we found that the taxon was not completely similar to any species known worldwide. Therefore, a new Argyreia species from China is described and illustrated here.

Material and method

Plant material was collected during field surveys in Yunnan Province from 2020 to 2021. The type specimens have been stored in the herbarium of Beijing Normal University (BNU). Morphological measurements were made from dried specimens of herbarium by Nikon digital camera, Stereoscope (ZEISS V8) and software ImageJ (Abràmoff et al. 2004). Materials for observation of pollen morphology were obtained from herbarium, picking mature pollen from the dried specimens, sticking it on the sample stages with conductive adhesive, spraying gold and photographing by Scanning Electron Microscope. The collected specimens were compared with the type specimens of morphologically similar species at main herbariums in China (BNU, HITBC, IBSC, KUN, PE, WUK, YUKU), as well as digital images available online provided by JSTOR and herbaria abroad that are relevant for the group (A, BM, E, G, K, P). Fresh plant materials of the similar species (A. wallichii) were also collected for further careful comparison. All type specimens (or photos of type specimens) of accepted names and their synonyms in Argyreia known around the world were examined, which refer to the voucher information provided by Staples and Traiperm (2017).

Taxonomic treatment

Argyreia subrotunda Q.R.Liu & M.L.Zhang, sp. nov.

Figs 1, 2

Type

China. Yunnan Province: Malipo County, Xinzhai Village, 22°57'48.01"N, 104°46'31.11"E, along roadside, 1300 m elev., 27 Aug 2021, fl. M. L. Zhang BNU2021YN074 (holotype: BNU0053319!; isotypes: BNU!).

Figure 1. 

Argyreia subrotunda Q.R.Liu & M.L.Zhang, sp. nov. A stem with leaves and inflorescences B bract (outside) C bract (inside) D sepals from outer (left) to innermost (right) E opened corolla showing mid-petaline bands F opened corolla with stamens G pistil H fruit with persistent sepals I seed (adaxial surface) J seed (lateral surface). All drawn by Quan-Ru Liu from voucher specimens M. L. Zhang BNU2021YN074 (BNU!) (A–G), X. B. Guo BNU2021YN081 (BNU!) (H–J).

Diagnosis

A. subrotunda is unique, a small-flowered type with an entire or shallowly lobed corolla as well as exserted stamens and pistils (included in dry specimens), smaller elliptic bracts, and outer sepals ovate-circular. It is similar to A. wallichii in indumentum features (whitish tomentose) and fruit types (red globose berry), but differs by its smaller elliptic bracts (vs. ovate-oblong), lax flat-topped cymes (vs. compact capitate) and shorter corolla tubes (2–2.5 cm vs. 4–5 cm). Additionally, A. subrotunda is similar to A. fulvocymosa in leaf shape (broadly ovate-circular to nearly circular) and inflorescence (flat-topped cymes), but the latter is covered with densely yellowish villus and has a distinctly 5-lobed corolla, which is very easy to distinguish (Table 1).

Table 1.

Comparisons of A. fulvocymosa, A. subrotunda and A. wallichii.

Character A. fulvocymosa A. subrotunda A. wallichii
Inflorescence flat-topped cymes flat-topped cymes capitate cymes
Bract Shape unknown elliptic ovate-oblong
Size unknown 0.8–1 cm × 0.4–0.8 cm 2.5–3.5 cm × 1.5–2.5 cm
Outer sepal Shape broadly ovate-circular ovate-circular elliptic-oblong
Corolla Length ca. 2 cm 2–2.5 cm 4–5 cm
Mid-petaline bands indumentum yellowish hirsute whitish villous whitish villous
Limb distinctly 5-lobed entire or shallowly lobed entire or shallowly lobed
Stamen and pistil exserted exserted included

Description

Climbing lianas; stem woody at base, herbaceous above, the former puberulent, the latter covered with whitish trichomes. Leaves simple, alternate; petiole 6–10 cm long, tomentose; leaf blades broadly ovate to rounded, 13–16 × 12–15 cm; base truncate or slightly cordate, occasionally oblique, margins entire, apex acute or obtuse, sometimes slightly emarginate; adaxially green, sparsely whitish velutinous only along leaf veins, abaxially paler, densely shining tomentose; secondary veins 13–15 on either side, curved to edge, veins slightly raised adaxially, more prominently raised abaxially. Inflorescences flat-topped cymes, axillary or terminal; peduncle 2–5 cm long, tomentose, angulate, secondary and tertiary peduncle 6–12 mm long; bracts small, elliptic, 8–10 × 4–8 mm, obtuse, hairy outside, veined; pedicels 5–7 mm long, up to 10 mm in fruit. Flowers diurnal; sepals unequal, 2 outer ovate-circular, 8–9 × 6–7mm, 3 inner elliptic, 6–7 × 3–5 mm, apex obtuse, abaxially whitish tomentose, adaxially glabrous, veined, enlarged in fruit, rose-red, shiny. Corolla tubular-funnelform, 2–2.5 cm long, pink, densely whitish villous outside on mid-petaline bands, otherwise glabrous, limb entire or shallowly lobed. Stamens exserted; filaments filiform, 14–15 mm long, attaching to the site of ca. 5 mm from stamens base, expanded at attachment points and densely whitish hairy there; anthers oblong, 3–4 mm long; pollen globose, pantoporate, with spines, 90–101 μm in diameter. Pistil exserted; disc ringlike, glabrous, ca. 1 mm high; ovary glabrous, ovoid, 2–3 mm high; style filiform, glabrous, 20–22 mm long; stigmas capitate, 2-lobed. Fruit enclosed in persistent, accrescent calyx, 2 outer fruiting sepals enlarging to 10–11 × 7–8 mm, 3 inner sepals 8–10 × 5–6 mm; berry subglobose, 7–10 mm in diam., purple-red, glabrous, exocarp leathery shiny, with obvious stomata under a magnifier, wrinkled when dry. Seeds 1–2, subglobose or hemispherical, 3.5–4 × 4–4.5 × 2.5–3 mm, black, glabrous, surface not smooth; hilum subcordate, brown, basal, margin with sparsely whitish hairy.

Figure 2. 

Argyreia subrotunda Q.R.Liu & M.L.Zhang, sp. nov. A plant habit B inflorescence C flower in frontal view D fruit with persistent sepals E seeds: adaxial surface (left); lateral surface (right). Scale bar: 5 mm. Photographs A–C, E by Mao-Lin Zhang, D by Xi-Bing Guo.

Phenology

Flowering from August to November; fruiting in November to February.

Distribution and habitat

Distributed in Yunnan and Gaungxi Province (Fig. 3), occurring at elevations of ca. 650–1300 m, distributed at open and sunny places such as roadsides, thickets, edges of mingled forest.

Figure 3. 

Distribution of Argyreia subrotunda in China. Drawn by Yi He.

Preliminary conservation status

Least Concern (LC). At present, five populations have been collected in Malipo County, Maguan County and Napo County. Each population is large with high flowering rates, and the number of mature individuals in the population is more than 50. According to the IUCN (2019) red list categories and criteria, A. subrotunda should be categorized as a ‘Least Concern (LC)’ species, which needs further investigation and research to more fully assess the conservation status.

Etymology

The specific epithet refers to the leaf shape, which is near-round.

Chinese name

近圆叶银背藤 (Jìn Yuán Yè Yín Bèi Téng).

Additional specimens examined

China, Guangxi Province: Napo County, Baisheng Township, Naen Reservoir, 26 Nov. 2013, fr. B. Y. Huang et al. 451026131126017LY (GXMG!); Yunnan Province: Malipo County, Bar-bu, 1000 m elev., 2 Feb. 1940, fr. C. W. Wang et al. 86509 (PE!); Malipo County, Wen-tian Road beside National Highway G246, 650 m elev., 23 Nov. 2021, fr. X. B. Guo BNU2021YN081 (BNU!); Malipo County, Xinzhai Village, 1300 m elev., 23 Nov. 2021, fl. X. B. Guo BNU2021YN082 (BNU!).

Pollen morphology

The observed pollen grains of A. subrotunda were monad, spheroidal to subspheroidal and radially symmetrical, with polypantoporate and echinate ornamentation (Fig. 4). It was possible to divide into two types based on the pollen morphology as follows: the diameter of the pollen grain was less than 100 μm with shorter bottle-like spines (5–7 μm), such as A. wallichii and the new species A. subrotunda; the diameter of pollen grains was over 100 μm with longer cone-shaped spines (≥ 10 μm), such as A. marlipoensis, which is endemic to Yunnan province, and the flower of which is first seen in this study.

Figure 4. 

Comparison of pollen morphology A Argyreia subrotunda B A. wallichii C A. marlipoensis. Scale bars: 20 μm.

Discussion

Morphologically, this species is most similar to A. wallichii and A. fulvocymosa, and it can be easily distinguished by the characters summarized in Table 1. The new species was similar to A. wallichii, both having similar indumentum features and fruit types as well as being almost sympatric. However, based on 17 specimens from two populations of A. subrotunda, we found the length of corolla was a very stable feature, about 2–2.5 cm, which was significantly shorter than A. wallichii (4–5 cm). The latter could also be easily distinguished from the new species by its compact capitate cymes and ovate-oblong bracts instead of flat-topped cymes and elliptic bracts. Additionally, A. subrotunda was similar to A. fulvocymosa in leaf shape and inflorescence, but the latter had a distinctly 5-lobed corolla instead of an entire or shallowly lobed corolla. Morphological comparisons of fresh plants between A. subrotunda and A. wallichii were provided in Figure 5. Furthermore, detailed comparisons of A. fulvocymosa, A. subrotunda and A. wallichii were provided in Table 1.

Figure 5. 

Argyreia subrotunda A opened corolla with 5 stamens B bract E inflorescence. A. wallichii C opened corolla with 5 stamens D bract F inflorescence.

The discovery of the new species has important value for further understanding of the morphological patterns of Argyreia in China. The new species is endemic to southwest China and compared to other species with an entire or shallowly lobed corolla in China, it seems to have comparative smaller corollas, which reinforces its recognition as a new taxa.

Key to the species of Argyreia from Yunnan, China

1 Corolla entire or shallowly lobed 2
Corolla deeply 5-lobed 17
2 Climbing herb, stems slender, roots thick 3
Climbing shrubs or lianas, stem woody at base 4
3 Leaf blade linear; sepals ovate; corolla pale purple, 4–4.5 cm long A. lineariloba
Leaf blade ovate to ovate-deltate; sepals linear-lanceolate; corolla red, ca. 7 cm long A. baoshanensis
4 Bracts soon deciduous 5
Bracts persistent 7
5 Leaf blade densely yellowish sericeous-velutinous abaxially A. velutina
Leaf blade sparsely strigose or hispid abaxially 6
6 Leaf blade lanceolate or ovate to ovate-elliptic A. henryi
Leaf blade broadly ovate to nearly circular, truncate or slightly cordate A. strigillosa
7 Bracts with more than 15 mm in length 8
Bracts 2–13 mm in length 13
8 Inflorescence paniculate-umbelliform, lax 9
Inflorescence capitate, condensed 10
9 Leaf blade sparsely hispid abaxially, somewhat reddish purple colored; bracts narrowly lanceolate; corolla campanulate-funnelform, 5–7 cm long A. marlipoensis
Leaf blade densely silvery sericeous; bracts ovate-circular; corolla urceolate-funnelform, 2.5–3.5 cm long A. monosperma
10 Indumentum brown or dull yellow, hirsute A. capitiformis
Indumentum whitish or pale yellow, villous or pubescent 11
11 Bracts ligulate, petiolate, apex acuminate A. roxburghii var. ampla
Bracts ovate-circular or broadly ovate, apex acute or obtuse 12
12 Bracts densely curly sericeous villous abaxially, ovate-circular; sepals brown, narrow-oblong A. eriocephala
Bracts densely pubescent abaxially, broadly ovate; sepals rose purplish, ovate-oblong A. wallichii
13 Leaf blade broadly ovate-circular, base truncate or slightly cordate, densely yellowish villous or whitish tomentose abaxially 14
Leaf blade narrowly oblong or ovate-oblong, to elliptic, base rounded or broadly cuneate, densely silvery sericeous-pilose abaxially 15
14 Leaf blade densely dull yellowish sericeous villous abaxially; corolla broadly funnelform, ca. 4.5 cm long, purple A. fulvovillosa
Leaf blade densely whitish tomentose abaxially; corolla tubular-funnelform, 2–2.5 cm long, pink A. subrotunda
15 Peduncle 10.5–13.5 cm long A. splendens
Peduncle less than 10 cm long 16
16 Sepals subequal, ovate-oblong; corolla white A. cheliensis
Sepals unequal, elliptic or oblong; corolla purple A. monglaensis
17 Inflorescence capitate; bracts persistent; peduncle short to none, 0–0.3 cm long A. osyrensis
Inflorescence paniculate-umbelliform; bracts tiny or caducous; peduncle elongated, ca. 0.5 cm long 18
18 Young stems, leaves abaxially, inflorescence all densely silvery sericeous-pilose; cymes axillary or terminal, 3–10-flowered A. obtusifolia
Young stems, leaves abaxially, inflorescence all densely yellowish tomentose; cymes axillary, 9–40-flowered A. fulvocymosa

Acknowledgements

We would like to express gratitude to the curators of the herbaria A, BM, E, G, HITBC, IBSC, K, KUN, P, PE, WUK, YUKU for assistance and access to specimens; Lai Wei (BNU) for providing valuable comments and suggestions; Xi-Bing Guo for taking part in field collection work and providing specimens. This research was supported by the National Natural Science Foundation of China (no. 31770213).

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