Are flowers physiological sinks or faucets? Costs and correlates of water use by flowers of Polemonium viscosum

Water loss through inflorescences may place extreme demands on plant water status in arid environments. Here we examine how corolla size, a trait known to influence pollination success, affects the water cost of flowering in the alpine skypilot, Polemonium viscosum. In a potometry experiment, water uptake rates of inflorescences were monitored during bud expansion and anthesis. Corolla volume of fully expanded flowers predicted water uptake during bud expansion (R ²=0.61, P=0.0375) and corolla surface area predicted water uptake during anthesis (R ²=0.59, P=0.044). To probe mechanisms underlying the relationship between corolla size and water uptake, cell dimensions and densities were measured in several regions of fully expanded corollas. Corolla length was positively correlated with cell length in the middle of the corolla tube and cell diameter in the corolla lobe (Pearson's r from 0.26–0.33, n=86, P ≤ 0.05). Cell density was negatively correlated with cell dimensions in the upper corolla tube and lobe (Pearson's r from –0.39 to –0.42, P ≤ 0.0015). These findings suggest that more water may be required to maintain turgor in large corollas in part because their tissues have lower cell wall densities. The carbon cost of water use by flowers was assessed in krummholz and tundra habitats for P. viscosum flowering, respectively, during dry and wet portions of the growing season. For plants in full flower, average leaf water potentials were significantly more negative (P=0.0079) at mid-day in the krummholz (June) than in the tundra (July), but were similar before dawn (P=0.631). Photosynthetic rate at the time of flowering declined significantly with increasing corolla size in the krummholz (P=0.0376), but was unrelated to corolla size on the tundra (P>0.72). Plants losing water through large corollas may close leaf stomata to maintain turgor. If photosynthesis limits growth in this perennial species, then the water cost of producing large flowers should exacerbate the cost of reproduction under dry conditions. Such factors could select for flowers with smaller corollas in the krummholz, countering pollinator-mediated selection and helping maintain genetic variation in corolla size components of P. viscosum. Received: 5 May 1998 / Accepted: 2 October 1998     

Corolla tube formation in four species of solanaceae

Corolla tube formation inSolanum nigrum, Salpichroa rhomboidea, Datura stramonium var.chalybea andNicotiana tabacum cv. Xanthi nc was investigated anatomically. InSolanum, the formation of the lower portion of the corolla tube, including the portion below the stamen insertion and the inserted zones, begins with the extension of the bases of the petal primordia toward the interprimordial regions. The extension of the petal bases is caused by the successive incorporation of the interprimordial regions just beside the bases into the petal primordia by means of the upward growth at those regions. The extending petal bases reach the lower portions of stamen primordia and connect with them resulting in formation of a short tube, which later develops into the lower portion of a corolla tube accompanied by epipetalous stamens. The petal bases extend further, and connect with each other outside the stamen primordia. The upward growth occurs also at the connected regions resulting in formation of the upper portion of a corolla tube. Marginal meristems of the petal primordium differentiate not later than the connection of petal bases. After the connection, marginal meristems and meristems of connected regions become continuous with each other and develop in a similar pattern. In the other three species, the corolla tube is formed in a similar manner as in the species mentioned above. However, the connection of the petal primordia occurs much earlier than the differentiation of their marginal meristems. InSalpichroa andNicotiana, the developmental patterns of the connected region and the corolla lobe margin are different.     

POLLINATION IN FLORAL SCENT MORPHS OF POLEMONIUM VISCOSUM: A MECHANISM FOR DISRUPTIVE SELECTION ON FLOWER SIZE

Plants of Polemonium viscosum have flowers that are either sweet or skunky in scent. The two morphs are preferentially pollinated by insects of strongly contrasting body size: bumblebee queens specialize on sweet flowers, flies on skunky ones. In this study 13 characters were examined in plant specimens from five populations to identify major components of intraspecific variation in flower and inflorescence morphology and test their correlation with floral scent. Factor analysis identified four major axes of morphological variation. The first explained 22% of the variance among specimens and correlated strongly with four flower size characters: sepal length, corolla tube length, corolla lobe width, and corolla lobe length. Floral scent morphs differed significantly in the multivariate representation of flower size defined by these characters. Sweet flowers had wider corolla lobes, longer corolla tubes, and longer sepals than skunky ones. Corolla lobe width accounted for the greatest amount of intermorph divergence. Divergence in flower size between morphs was maintained in mixed populations at four locations in alpine Colorado, with corollas of sweet flowers significantly broader or more flared than those of skunky flowers. Patterns of pollen receipt suggest that this difference is adaptive. In the sweet morph, pollination intensity and purity increased significantly with corolla flare. Conversely, in the skunky morph, corolla flare had little influence on pollination intensity and had a strong negative effect on purity. These findings suggest that selection for effective pollination should favor intraspecific divergence in flower size in Polemonium viscosum.     

Corolla tube formation in six species of apocynaceae

Corolla tube formation inTrachelospermum asiaticum, Nerium indicum var.leucanthum, Anodendrom affine, Vinca major, Catharanthus roseus andAmsonia elliptica was investigated anatomically. The corolla tube formation among these species is basically similar. The bases of petal primordia extend laterally to the interprimordial regions, the upward growth occurrig at those regions just beside the petal bases. The extending petal bases connect with each other at the bases of the abaxial side of stamen primordia in the early stage of the corolla development. The upward growth at the coonnected regions results in the formation of a short corolla tube but is weakened rapidly. At the stage of the mutual connection of petal bases, a common base of petal and stamen primordia is initiated. This common base develops into the lower portion of the corolla tube, i.e. the portion below the stamen insertion. In a relatively late stage, adjacent margins, of the corolla lobes fuse postgenitally at their lower portions, resulting in the formation of almost all of the upper portion of the corolla tube. The corona inNerium andVinca is initiated by the active adaxial growth of the upper portion of the corolla tube.     

Corolla tube formation in the Tubiflorae and Gentianales

Corolla tube formation was investigated anatomically for 22 species of the Polemoniaceae, Convolvulcaeae, Boraginaceae, Verbenaceae, Buddlejaceae. Scrophulariaceae, Gentianaceae, Menyanthaceae and Asclepiadaceae. The corolla tbe formation is basically similar among species, except for the cases ofNymphoides, Dichondra andCuscuta. The petal bases extend laterally to the interprimordial regions, the upward growth occurring at those regions just beside the petal bases, and connect mutually at the back of stamen primordia. The upward growth at the connected regions co-opeates with the growth of the expanding petal margins, resulting in the formation of the upper portion of the corolla tube. How-ever, developmental patterns are not always similar. InSwertia, Nymphoides andMenyanthes, the upward growth at the connected regions is meager. InDichondra andCuscuta, the mutual connection of petal bases is not seen. The lower portion of the corolla tube is formed by the elongation of the common base of petal and stamen primordia, resulting in the formation of the epipetalous condition of stamens, except for the case ofNymphoides. InNymphoides, the lower portion of the corolla tube results from the cup-like structure formed on the floral meristem before the initiation of petal primordia.     

Phylogenetic implications of corolla morphology in subfamily Barnadesioideae (Asteraceae)

The previously insignificant and small South American subtribe Barnadesiinae of tribe Mutisieae has been shown recently to be ancient within Asteraceae. Due to absence of a 22 kb diagnostic chloroplast inversion, plus other features, this subtribe has been elevated to subfamilial status as Barnadesioideae, now containing 90 species in nine genera. Recent cladistic analyses at the generic and specific levels based on morphology and DNA sequences (ITS and trnL intron) have revealed different relationships among taxa of the subfamily. To better understand these conflicts, we analyze specific morphological features of corollas (shape and vascularization) to develop trends (trees) in these features based on minimal structural change (i.e., morphological parsimony), and to compare these with relationships among genera derived from the two recent cladistic analyses. We define six principal types of corollas in Barnadesioideae (tubular, split, double split, ligulate, subbilabiate and bilabiate) and six principal types of corolla vascularization patterns (combinations of presence or absence of central bundles, fusion of adjacent bundles and fusion of bundles at the apex of corolla lobes). In all features we assume character states in Calyceraceae to be ancestral. In corolla shape, from tubular ancestry, we hypothesize two general evolutionary trends within the subfamily: (1) splitting of the tube, and (2) flattening of the tube. In vascularization of corollas, from an ancestral condition of one central and one lateral bundle in each corolla lobe and all traces fused at the apex, we hypothesize four basic trends: (1) gain or (2) loss of lateral vascular traces in each lobe, (3) loss of the central vein, and (4) loss of fusion of traces in lobe apices. These morphological trends allow tests of the two previous phylogenetic hypotheses by (1) counting step changes (following steps in the morphological network) in the two characters on the two competing phylogenetic trees and (2) constructing an index of morphological advancement for each genus (based on morphological trees of the two characters) and correlating these with cladistic distances within the two phylogenies. Results of both tests reveal the molecular phylogeny to be more compatible with evolutionary inferences from the two morphological features. With Fulcaldea excluded, a highly significant correlation is seen between morphological advancement and cladistic distance in the molecular phylogeny.     

Evolution of flower shape inVeroniceae (Scrophulariaceae)

Floral evolution in the tribeVeroniceae was examined using phylogenetic analysis combining 24 adult morphology and chromosome number characters with 22 qualitative and quantitative floral development characters. Taxa sampled included nine species ofVeroniceae and as an outgroup one species each ofDigitaleae andVerbasceae. Veronica, Besseya, andSynthyris formed one clade, subtended byPseudolysimachion and then by theHebe group;Veronicastrum orWulfenia represent the basal-most branch of the tribe. The ancestral flowers of theVeroniceae may have been small with moderately short corolla tubes and lobes; long corolla tubes arose four times in the tribe and large corolla lobes twice.     

Corolla tube formation in the primulaceae and ericales

Corolla tube formation was investigated anatomically for 13 species of the Primulaceae and Ericales. In the Primulaceae, petal primordia appear after the stamen initiation. The lower portion of the corolla tube, the portion under the stamen insertion, is derived from the ring-like structure formed immediately after the stamen initiation. Petal bases extend laterally, and connect mutually on the ring-like structure. The upward growth at the connected regions results in the formation of a corolla tube, which develops into the upper portion of the corolla tube. In the Ericales, except forClethra, the corolla tube is formed by the mutual connection of petal bases. This tube elongates inRhododendron, Leucothoe andPieris. However, inPyrola, Ledum andTripetaleia, the elongation of this tube is meager, resulting in a dialypetalous condition in the mature state. Three petals ofTripetaleia may be derived from the partial connection of five petal primordia in a very early stage of the corolla development. From the data obtained in the studies on the corolla tube formation, three modes of the corolla tube formation are suggested; postgenital fusion, connection of petal bases, elongation of the ring-like common base.     

Secondary contact and adaptation to local pollinator assemblages mediate geographical variation in corolla length in Isodon shikokianus

Adaptation to local pollination regimes and secondary contact of allopatrically differentiated populations with respect to pollination ecology may result in geographical variation in floral traits. We examined the contributions of these two processes in Isodon shikokianus, which showed remarkable geographical variation in corolla tube length in western Japan. Corolla tube length varied among 17 study populations located within a relatively narrow area, and covaried with altitude and distribution of two bumblebee pollinators with different tongue lengths: the longer corolla was found at lower altitudes where the long-tongued pollinator was more abundant, and vice versa. Additionally, bumblebee species preferentially visited flowers that fit their tongue lengths. Population genetic analysis based on 11 microsatellite loci revealed that populations with long and short corolla tubes constituted genetically distinct groups. Migration rates were low between the groups, but high within each group. These results indicate that two genetically differentiated groups made secondary contact and hybridized, and gene flow between the groups was limited. Thus, the geographical variation in corolla tube length in I. shikokianus may be a result of past allopatric differentiation and subsequent secondary contact of populations with different corolla tube lengths. The variation in corolla tube length within a narrow area may be maintained by selection owing to the altitudinally structured pollinator assemblages. Altitudinal differences in relative abundance of two pollinators and their assortative visitation with respect to corolla tube length may contribute to reproductive isolation between the two groups.     

STRUCTURE AND DEVELOPMENT OF THE PERIANTH IN DOWNINGIA BACIGALUPII

The structure and ontogeny of the calyx and corolla of Downingia bacigalupii Weiler (Campanulaceae; Lobelioideae) were investigated for the purpose of comparing perianth development with previous observations on the floral bract, as well as elucidating the mechanism of development of the zygomorphic, sympetalous corolla. Sepals are uni-traced with a palmate, reticulate venation. They have basal and apical hydathodes, as well as storage tracheids. Sepals show a reduction in size, venation and hydathode number when compared to the bract. The pentamerous, zygomorphic corolla is bilabiate, consisting of a three-lobed adaxial lip and a two-lobed abaxial lip connected by a short tubular region. The constituent petal lobes are also uni-traced and have a reticulate venation, resembling that of the sepal and bract, but lack storage tracheids and hydathodes. Sepals arise in an adaxial to abaxial succession and are initiated in the outer corpus layer of the floral apex. Expansion of the floral apex follows and is accompanied by the establishment of a second tunica layer. Sepals undergo apical, marginal, and intercalary growth accompanied by acropetal differentiation of procambium. The petals arise simultaneously and are initiated in the second tunica layer and the outer corpus cells. After initiation, the petals exhibit a period of apical and marginal growth followed by intercalary growth. Apical growth in petals is less protracted than in sepals, but plate meristem activity is more extensive. The free petal lobes become temporarily fused by an interlocking of marginal epidermal layers, but they separate at anthesis. Zonal growth beneath the originally free lobes forms the tube and lip regions of the sympetalous corolla. Zygomorphy is evident from the time of initiation of petals and is accentuated by later differential growth. Comparative observations of corolla ontogeny in autogamous species of Doumingia indicate that the reduced corollas in these taxa are derived by a simple process of neoteny.     

Quantitative floral development in Pseudolysimachion (Scrophulariaceae): intraspecific variation and comparison with Veronica and Veronicastrum

Intraspecific variation in floral development was studied in four morphologically distinct strains of Pseudolysimachion longifolium and two of P. spicatum. Size increase of whole buds from living plants of P. longifolium was followed in absolute time. Growth rates were homogeneous within inflorescences and within individual plants, and significantly different between individual plants. Organ growth trajectories (plotted as organ size over gynoecium size) differed little among individuals of Pseudolysimachion belonging to morphologically distinct strains; variation was most pronounced in the calyx. Corolla tube as well as calyx and corolla lobe measurements varied more during the early stages of development than near maturity, suggesting constraints on mature flower form. In addition to intraspecific variation, floral development in Pseudolysimachion was compared with that in related Veronica chamaedrys and Veronicastrum virginicum, using data from a previous study. Mature flowers of Pseudolysimachion have long corolla tubes similar to those of Veronicastrum and long corolla lobes similar to those of Veronica. The trajectories of most organs of Pseudolysimachion were intermediate between those of Veronica and Veronicastrum in position as well as in type of curve, i.e., different trajectories lead to similar end products; thus, the shapes of the mature organs are not strictly homologous and not indicative of close relationship.     

Taxonomy of the Genus Oreocharis (Gesneriaceae)

The genus Oreocharis as circumscribed here consists of 27 species including 5 varieties, of which 5 species and 4 varieties are described as new in the present paper. In the work analysed were the external morphology and geographic distribution and examined under SEM were pollen exine of 22 species and seed coat of 16 species. As a result, three types of the corolla, two types of the anther, three types of the pollen exine and three types of the seed coat are distinguished here in the paper. It is discovered that the corolla in the genus is relatively stable, though diverse, and highly correlated with the characters of pollen grains and seeds. The corolla clearly bilabiate but constricted at the throat, occurring in O. auricula, O. cordatula, O. aurantiaca, etc., for an example, is correlated with smooth, reticulate pollen exine and partial tectum and the reticulate and smooth seed coat. For this reason the subdivision of the genus in the paper is mainly based on the characters of the corolla, but combined with those of the anther, pollen and seed coat. The genus is divided into four sections in the present classification. Dasydesmus Craib, based on a single species. O. bodinieri, is reduced here, and the reasons are given. The genus is distributed mainly in the subtropics, and less frequently in the tropics, of China south of 32.5°N and east of 98.5°E, with only two species beyond the border, O. hirsuta in Thailand (only a single locality in Chiengmai) and O. aurea also found in north Vietnam (see Fig. 1, Table 3). Sect. 1. Stomactin (Clarke) Fritsch. Corolla urceolate-tubular, constricted at the throat, with limb distinctly bilabiate; anthers broad-oblong; seed coat reticulate, smooth, rarely minutely tuberculate; pollen exine fine-reticulate, tectum partial and smooth, luminae slightly unequal in size. Sect. 2. Orthanthera K. Y. Pan Corolla campanulate or campanulate-tubular; anthers broad-oblong; seed coat reticulate, muri smooth, rarely spiny-processed; pollen exine fine-reticulate, with partial and smooth tectum and luminae slightly unequal in size, rarely exine insular and fine-tuberculate, tectum perforate. Setc. 3. Oreocharis Corolla thin-tubular; anthers broad-oblong; seed coat densely spinyprocessed, rarely fine-tuberculate; pollen exine insular, densely spiny-processed, rarely finereticulate and smooth, luminae unequal in size. Sect. 4. Platyanthera K. Y. Pan Corolla campanulate; anthers hippocrepiform; seed coat densely spiny-processed; pollen exine fine-reticulate, tectum perforate, luminae small, nearly equal in size. In the section Stomactin, although the constriction of corolla at its throat is a specialized character, the characters of seed coat, pollen grains and anthers are apparently primitive. Therefore it may be said at least that more primitive characters are preserved in the section. In the section Oreocharis, on the contrary, the characters of corolla, seed coat and pollen exine are all advanced. And in the section Platyanthera, the seed coat, pollen (with perforate tectum) and anthers have developed rather specialized characters.     

Continuous characters in phylogenetic analyses: patterns of corolla tube length evolution in Lithospermum L. (Boraginaceae)

The present study comprises an analysis of six different scoring schemes and eight different types of analytic methods aiming to investigate the evolution of a continuous character (i.e. corolla tube length) in Lithospermum L. (Boraginaceae). Corolla tube length in the genus is quite variable, ranging from 1 mm to 75 mm, and the length of the corolla tube has implications for pollination biology, such as longer corolla tubes (> 25 mm in length) being pollinated by hummingbirds or moths. In general, the various methods resolve similar ancestral character states; however, different states are reconstructed at nodes in which the descendants greatly differ in corolla tube length. Additionally, it is suggested that all of the variation of a continuous character should be included in analyses, and this may necessitate multiple analyses with different partitions of the data. The various analyses provide evidence that two maximum parsimony methods, linear parsimony and the TNT method, minimize the number of different rates of evolution. In Lithospermum, six origins of corolla tubes > 20 mm in length are resolved, and these origins occurred at two different times periods: (1) in the shadow of hummingbird diversification in North America (approximately 6–8 Mya) and (2) more recently (approximately 1–1.5 MyA). Four substantial decreases in corolla tube length also are reconstructed, and these may be associated with the origin of self‐pollination. © 2012 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, ??, ??–??.     

PATTERNS OF FLORAL DEVELOPMENT IN AGALINIS AND ALLIES (SCROPHULARIACEAE). II. FLORAL DEVELOPMENT OF AGALINIS DENSIFLORA

Initiation of floral primordia begins in Agalinis densiflora with production of two lateral adaxial calyx lobe primordia followed by a midadaxial primordium, and then primordia of two abaxial calyx lobes. Initiation of three abaxial corolla lobe primordia is succeeded by that of two stamen pairs and then by primordia of two adaxial corolla lobes. The primordium of the abaxial carpel appears before the adaxial one. Except for the calyx, initiation of primordia proceeds unidirectionally from the abaxial to the adaxial side of the floral apex. Zygomorphy in the calyx, corolla, and androecium is evident during initiation of primordia and is accentuated during organogenesis. The calyx undergoes comparatively rapid organogenesis, but the inner three floral series undergo a protracted period of organogenesis. The perianth series reach maturation prior to meiosis in the anthers. Maturation of the androecium and gynoecium are postmeiotic events.     

紫花苣苔属——广东省被子植物一新记录属

在广东省德庆县进行全国第四次中药资源普查时采集了大量标本,经过鉴定和查阅相关资料,确定其中一号标本为紫花苣苔属(Loxostigma Clarke)东兴紫花苣苔[Loxostigma dongxingensis(Chun ex K.Y.Pan)M9llerY.M.Shui]。该属及该种在广东尚无分布报道,这是首次发现。紫花苣苔属为草本或亚灌木,根状茎匍匐或不存在,花冠粗筒状,檐部二唇形,雄蕊4,花药顶端成对连着,两对雄蕊紧密靠合,种子两端具毛状附属物。紫花苣苔属目前共11种,我国、尼泊尔、锡金、不丹、印度、缅甸及越南北部均有分布,在我国11种全产,分布于四川、云南、贵州和广西,广东首次记录。目前广东省是紫花苣苔属自然分布的最东界。东兴紫花苣苔为多年生草本,具横走根状茎,茎高为20~60 cm,花冠粗筒状,黄色,下方肿胀,近基部之上、中部之下突然收缩呈缢缩状,檐部2唇形,雄蕊4,花药成对连着,分布于广西及越南北部,广东首次记录,发现地位于德庆县象牙山林场,种群沿山间溪流两侧分布,生于林下沟谷旁光线较暗处。     

Kuepferia kanchii sp. nov. (Gentianaceae) from Sikkim Himalaya

Kuepferia kanchii D. Maity, Sentu K. Dey & Adr. Favre, a new species from Sikkim Himalaya, is described and illustrated. It differs from its close relative K. infelix (C. B. Clarke) Adr. Favre ( = Gentiana infelix C. B. Clarke) by having sessile and smaller flowers, and smaller floral parts. Kuepferia kanchii is further characterized by a white corolla with bluish green patches on the outside at the base of each corolla lobe, and a corolla tube flushed with light green inside towards the base, blue filaments, sessile stigma, smaller capsule, and trigonous–elongated, ca 0.8 mm long and curved seeds.     

STUDIES IN THE FLORAL ANATOMY OF CLAYTONIA (PORTULACACEAE)

Claytonia virginica has a regular flower with two sepals, five petals with an equal number of stamens in positions opposite the petals and a many-seeded tricarpellate gynoecium with basal placentation. The flower has been interpreted as uniseriate, the putative sepals as bracts and the corolla as modified calyx lobes. Anatomical and developmental studies were undertaken to find evidence for the existence of vestigial or rudimentary parts whose existence would illuminate the true nature of the flower. Vascular and epidermal anatomy of sepals are both similar to that of leaves. Corolla and androecium develop basipetally and petals and stamens share common vascular traces in the lower part of the receptacle. Thus, in terms of both anatomy and development, evidence supports the conclusion that the perianth is essentially biseriate. Vestigial or rudimentary parts are not present which would alter the manifest design of the mature flower.     

狮耳草属——中国唇形科植物一新归化属

该文报道了中国唇形科植物一新归化种——荆芥叶狮耳草[Leonotis nepetifolia(L.)R.Br.],该种的发现代表狮耳草属[Leonotis(Pers.)R.Br.]在中国的新归化。狮耳草属的主要特征为轮伞花序腋生,苞片和萼齿顶端针刺状,花冠桔红色或黄色,冠唇上唇较大,下唇较小;其与绣球防风属(Leucas R.Br)较为接近,但后者的萼齿等大,花冠通常白色,花冠筒不超出萼外,冠檐下唇长于上唇,二者区别较为显著。荆芥叶狮耳草为一年生草本。轮伞花序球形,多花密集,其下承以多数密集苞片;苞片细长,向下微弯曲,先端针刺状。花萼管状,先端膨大而略折曲;萼齿针刺状,最上面一枚较大。花冠桔红色,密被桔红色绒毛;花冠筒细长,伸出萼筒之外;冠檐二唇形,上唇较大,下唇较小。荆芥叶狮耳草与同属植物Leonotis leonurus R.Br.最为相似,但前者叶为卵圆形或心形,后者的叶片多为披针形。根据该研究的标本和相关文献资料,该文还提供了狮耳草属和荆芥叶狮耳草的形态描述、地理分布的讨论,以及荆芥叶狮耳草的资源价值、归化途经、繁殖和危害的讨论和野外生态照片。     

<Emphasis Type="Italic">Ceropegia bhatii</Emphasis>, a new species of Apocynaceae: Ceropegieae from Karnataka,India

Ceropegia bhatii S. R. Yadav & Shendage, discovered from Malebennur Ghat in Davangere district of Karnataka State is described and illustrated. It is similar to Ceropegia noorjahaniae M. A. Ansari but is distinct in its twining habit, two-flowered cyme, slightly inflated corolla tube and corolla lobe margins that are not recurved.     

Salvia petrophila sp. nov. (Lamiaceae) from north Guangxi and south Guizhou,China

Salvia petrophila G. X. Hu, E. D. Liu & Yan Liu, a new species from the Chinese provinces of north Guangxi and south Guizhou, is described and illustrated. The new species is similar to S. miltiorrhiza, but can easily be distinguished by its shorter, unbranched stem, subsucculent simple leaf, longer pedicel and corolla tube, oblong‐entire middle lobe of lower corolla lip and larger oblate pollen. It is included in S. sect. Drymosphace on the basis of its falcate‐compressed upper corolla lip and connivent posterior connectives. Trichome and pollen micromorphology of the new species and similar species are described and compared. Additionally, assessment of the conservation status, current geographical distribution and notes on ecology of the new species are given.