Abstract
BackgroundThe Gesneriaceae genus Chiritopsis, confined almost exclusively to cave or cave-like microhabitats of limestone karsts of southern China, was described to distinguish it from Chirita by much smaller flowers and generally miniature plant sizes in the former genus. However, molecular phylogenetic analyses showed that Chiritopsis is polyphyletic and its species delimitation has been problematic. To understand how many times Chiritopsis-like species have evolved from within the recircumscribed Primulina and to further clarify their species identification, we sampled all but two recently described species of Chiritopsis-like Primulina and reconstructed their phylogenetic relationship based on DNA sequences of nuclear ITS and chloroplast trnL-F and trnH-psbA.ResultsWith 182 accessions of 165 taxa of Primulina sampled, our analyses placed the 40 accessions of 25 taxa of Chiritopsis-like Primulina in 17 unrelated positions, indicating at least 17 independent origins of the traits associated with caves or cave-like microhabitats. Of the 17 clades containing Chiritopsis-like Primulina, Clade 1 is composed of P. bipinnatifida, P. cangwuensis, P. jianghuaensis, P. lingchuanensis, and P. zhoui, as well as additional samples that show variable and overlapping morphology in leaf shapes. Clade 10 includes P. cordifolia, P. huangii, and P. repanda, while Primulina repanda var. guilinensis is not placed within Clade 10. Primulina glandulosa var. yangshuoensis is not placed in the same clade of P. glandulosa.ConclusionsBased on our data, P. cangwuensis, P. jianghuaensis, and P. lingchuanensis are proposed to synonymize under P. bipinnatifida, with P. zhoui treated as a variety of P. bipinnatifida. Primulina repanda var. guilinensis is transferred as P. subulata var. guilinensis comb. nov. and Primulina pseudoglandulosa nom. nov. is proposed for P. glandulosa var. yangshuoensis. One new species is named P. chingipengii to honor the late Dr. Ching-I Peng (1950–2018).
Highlights
The Gesneriaceae genus Chiritopsis, confined almost exclusively to cave or cave-like microhabitats of limestone karsts of southern China, was described to distinguish it from Chirita by much smaller flowers and generally miniature plant sizes in the former genus
The Bayesian majority-rule consensus tree with mean branch length is depicted in Fig. 4, annotated with bootstrap support values (BS) of the maximum likelihood (ML) analyses and a
Because C. bipinnatifida is the earliest valid name of the clade, P. lingchuanensis, P. jianghuaensis, and P. cangwuensis are proposed to be synonymized under P. bipinnatifida, with P. zhoui treated as a variety of P. bipinnatifida for its disjunct distribution and unique leaf shapes
Summary
The Gesneriaceae genus Chiritopsis, confined almost exclusively to cave or cave-like microhabitats of limestone karsts of southern China, was described to distinguish it from Chirita by much smaller flowers and generally miniature plant sizes in the former genus. The Gesneriaceae genus Chiritopsis W.T.Wang was established to distinguish it from Chirita Buch.-Ham. ex D.Don by the much smaller flowers, significantly shorter ovaries comparing to the styles, and generally smaller plant sizes in the former genus (Wang 1981). Chiritopsis appears to be a morphologically coherent group readily recognizable (Wang 1992; Wei et al 2010), molecular phylogenetic analyses by Li and Wang (2007) showed that the genus (seven species sampled) is polyphyletic, nested within Chirita sect. To rectify the polyphyly, Wang et al (2011) and Weber et al (2011) proposed to abandon Chirita, transferring all its species to Codonoboea Ridl., Damrongia Kerr ex Craib, Henckelia Spreng., Liebigia Endl., Microchirita (C.B.Clarke) Yin Z.Wang, and Primulina Hance
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