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FIGURE 4 in A New Species of the Genus Tropidophorus Duméril, Bibron, 1839 (Reptilia: Squamata: Scincidae) from China-Vietnam Border Region in Southeastern Yunnan Province, China
FIGURE 4. Detailed closeup views of the holotype (KIZ 54236, A–C) and paratype (KIZ 55737, D–F) of Tropidophorus vongx sp. nov. in life, showing lateral head, dorsal head, and lateral body. Photos by KW.
FIGURE 3 in A New Species of the Genus Tropidophorus Duméril, Bibron, 1839 (Reptilia: Squamata: Scincidae) from China-Vietnam Border Region in Southeastern Yunnan Province, China
FIGURE 3. Holotype (KIZ 54236) and paratype (KIZ 55737) of Tropidophorus vongx sp. nov. in life. Photos by KW.
FIGURE 1. Rhododendron longipedicellatum Lei Cai & Y.P in Rhododendron longipedicellatum (Ericaceae) a new species from Southeastern Yunnan, China
FIGURE 1. Rhododendron longipedicellatum Lei Cai & Y.P. Ma. A. Branch with leaves and inflorescences; B. Young fruit with calyx; C. Dorsal side of stamen; D. Ventral side of stamen; E. Lateral view of flower; F. Opened corolla showing stamens.
FIGURE 2. Rhododendron longipedicellatum Lei Cai & Y.P in Rhododendron longipedicellatum (Ericaceae) a new species from Southeastern Yunnan, China
FIGURE 2. Rhododendron longipedicellatum Lei Cai & Y.P. Ma. (A, C, E–J) and R. rushforthii (B & D) A & B. Pressed branch with leaves and flowers; C. Branch with young fruits and flower; D. Flowering branch; E. Habitat and habit; F–G. Flowers; H. Lateral view of flowers showing corollas and pedicels; I–J. Fruiting branches.
FIGURE S1 in Two new diploid species of Isoetes (Isoetaceae: Lycopodiopsida) from Southeastern China based on morphological and molecular evidence
FIGURE S1. Spore morphology of Isoetes in China. (A) I. changleensis (B) I. yuhangensis (C) I. taiwanensis (cited from Liu et al. 2008). (D) I. sinensis (cited from Liu et al. 2008). (E) I. baodongii (cite from Lu et al. 2021). (F) I. longpingii (cite from Shu et al. 2022). (G) I. xiangfei (cite from Shu et al. 2022). (H) I. orientalis (cited from Liu et al. 2008). (I) I. yunguiensis (cited from Liu et al. 2008). (J) I. hypsophila (cited from Li et al. 2019). (K) I. shangrilaensis (cited from Li et al. 2019). Scale bars: A1–A3 = 100 μm; A4–A5 = 5 μm; B1–B3 = 100 μm; B4–B5 = 5 μm; C1–C3 = 150 μm; C4 = 12 μm; C5 = 8.6 μm; D1–D3 = 150 μm; D4–D5 = 10 μm; E1–E2 = 100 μm; E3–E4 = 10 μm; F1–F2 = 100 μm; F3–F4 = 10 μm; G1–G2 = 100 μm; G3–G4 = 10 μm; H1–H2 = 75 μm; H3–H4 = 4 μm; I1,I3 = 176 μm; I2 = 136 μm; I4–I5 = 10 μm; J1–J3 = 200 μm; J4–J5 = 10 μm; K1–K3 = 200 μm; K4–K5 = 10 μm.
FIGURE 2. Aspidistra xichouensis Lei Cai, Z.L.Dao & G.W in Aspidistra xichouensis (Asparagaceae), a new species from the karst region in southeastern Yunnan, China
FIGURE 2. Aspidistra xichouensis Lei Cai, Z.L.Dao & G.W.Hu. A. Habitat in Xichou County, Yunnan Province. B & C. Inflorescence. D. Lateral view of flower with bracts. E. Stigma. F. Fruit. G. Frontal view of flower. H. Longitudinal section of flower (showing stamens and pistil). I. Longitudinal section of young fruit. All photographs were taken by Lei Cai.
FIGURE 1. Aspidistra xichouensis Lei Cai, Z.L.Dao & G.W in Aspidistra xichouensis (Asparagaceae), a new species from the karst region in southeastern Yunnan, China
FIGURE 1. Aspidistra xichouensis Lei Cai, Z.L.Dao & G.W.Hu. A. Habit. B. Lateral view of flower with bracts. C & D. Longitudinal section of flower (showing stamens and pistil). E. Lateral view of pistil. F. Stigma, frontal view. G. Fruit. Drawn by Xuan-Lin Zhu.
FIGURE 3. Aspidistra minutiflora Stapf. A in Aspidistra xichouensis (Asparagaceae), a new species from the karst region in southeastern Yunnan, China
FIGURE 3. Aspidistra minutiflora Stapf. A. Habitat in Kunming Botanical Garden. B & C. Inflorescence. D. Lateral view of flowers. E & G. Longitudinal section of flower (showing stamens and pistil). F. Front view of flower. H. Lateral view of pistil. I. Stigma. All photographs were taken by Lei Cai.
TABLE 1 in Two new diploid species of Isoetes (Isoetaceae: Lycopodiopsida) from Southeastern China based on morphological and molecular evidence
<p><b>TABLE 1.</b> Comparative accounts on the morphology of megaspores and microspores of <i>Isoetes</i> species in China.</p><table><tbody><tr><th></th><th><i>I. changleensis</i></th><th><i>I. yuhangensis</i></th><th><i>I. baodongii</i></th><th><i>I. sinensis</i></th><th><i>I. longpingii</i></th><th><i>I. xiangfei</i></th><th><i>I. orientalis</i></th><th><i>I. taiwanensis</i></th><th><i>I. yunguiensis</i></th><th><i>I. hypsophila</i></th><th><i>I. shangrilaensis</i></th></tr></tbody><tbody><tr><th>Megaspore diameter (μm)</th><td>246–314</td><td>270–324</td><td>390–510</td><td>317–424</td><td>310–410</td><td>390–450</td><td>350–460</td><td>280–340</td><td>340–430</td><td>361–510</td><td>207–273</td></tr><tr><th>Mean megaspore size (μm)</th><td>284</td><td>302</td><td>450</td><td>378</td><td>350</td><td>430</td><td>420</td><td>312</td><td>390</td><td>450</td><td>245</td></tr><tr><th>Ornamentation of megaspores</th></tr><tr><th>proximal surface</th><td>tuberculate</td><td>rugulate</td><td>echinate-cristate</td><td>echinate</td><td>tuberculate-cristate</td><td>cristate-reticulate</td><td>cristate-reticulate</td><td>tuberculate</td><td>cristate-reticulate</td><td>levigate</td><td>levigate</td></tr><tr><th>Equatorial surface (girdle)</th><td>rugulate</td><td>smooth</td><td>/</td><td>loss</td><td>/</td><td>/</td><td>/</td><td>smooth</td><td>loss</td><td>loss</td><td>smooth</td></tr><tr><th>distal surface</th><td>rugulate</td><td>rugulate</td><td>echinate-cristate</td><td>echinate-cristate</td><td>tuberculate-cristate</td><td>cristate-reticulate</td><td>cristate-reticulate</td><td>tuberculate-cristate</td><td>cristate-reticulate</td><td>levigate</td><td>tuberculate-rugulate</td></tr><tr><th>Range microspore size (μm)</th><td>14–20</td><td>16–26</td><td>22–27</td><td>20–29</td><td>27–30</td><td>26–28</td><td>20–38</td><td>20–28</td><td>20–25</td><td>19–25</td><td>11–24</td></tr><tr><th>Mean microspore size (μm)</th><td>18</td><td>21</td><td>25</td><td>25</td><td>29</td><td>27</td><td>34</td><td>24</td><td>22</td><td>22</td><td>19</td></tr><tr><th>Ornamentation of microspores</th><td>blunt-tipped echinate</td><td>sharp-tipped echinate</td><td>echinate</td><td>echinate</td><td>echinate</td><td>echinate</td><td>echinate-tuberculate</td><td>echinate</td><td>levigate-granulate</td><td>rugulate</td><td>echinate-cristate</td></tr><tr><th>Chromosome number</th><td>22</td><td>22</td><td>22</td><td>44</td><td>44</td><td>44</td><td>66</td><td>22</td><td>22</td><td>22</td><td>22</td></tr><tr><th>Data Source</th><td>this study</td><td>this study</td><td>Lu <i>et al.</i> 2021</td><td>Liu <i>et al.</i> 2008</td><td>Shu <i>et al.</i> 2022</td><td>Shu <i>et al.</i> 2022</td><td>Liu <i>et al.</i> 2008</td><td>Liu <i>et al.</i> 2008</td><td>Liu <i>et al.</i> 2008</td><td>Li <i>et al.</i> 2019</td><td>Li <i>et al.</i> 2019 Shu <i>et al.</i> 2022</td></tr></tbody></table><p>Note:/ represents no data.</p>
FIGURE 1. Leptochilus brevipes.—A in Leptochilus brevipes (Polypodiaceae), a new fern species from southeastern Yunnan, China based on morphological and molecular evidence
FIGURE 1. Leptochilus brevipes.—A. Habit of the new fern on rock.—B. Habit of the new fern on tree trunk.—C. Rhizome.—D. Portion of fertile frond.—E. Lower portion of abaxial lamina of sterile frond.—F. Upper portion of abaxial lamina of sterile frond.—G. Middle portion of abaxial lamina of sterile frond. Photo credit: Zhen-Long Liang & Jing Zhao.
FIGURE 2. Leptochilus brevipes.—A. Habit.—B in Leptochilus brevipes (Polypodiaceae), a new fern species from southeastern Yunnan, China based on morphological and molecular evidence
FIGURE 2. Leptochilus brevipes.—A. Habit.—B. Portion of lamina.—C. Cross section of costa.—D. Cross section of rhizome. Stippled: vascular tissue; black: sclerenchyma strands.—E. Rhizome scale (drawn by Zhen-Long Liang based on the isotype at CDBI).
FIGURE 3 in Leptochilus brevipes (Polypodiaceae), a new fern species from southeastern Yunnan, China based on morphological and molecular evidence
FIGURE 3. Maximum likelihood phylogeny of Leptochilus based on six plastid markers (atpB, rbcL, rps4, rps4-trnS, trnL, trnL-F). Maximum likelihood bootstrap support (MLBS) are above the branches. Six subclades of the Colysis clade identified by Zhang et al. (2019) are indicated in green.
Supplementary material 3 from: Luo T, Wang Y, Wang S, Lu X, Wang W, Deng H, Zhou J (2021) A species of the genus Panophrys (Anura, Megophryidae) from southeastern Guizhou Province, China. ZooKeys 1047: 27-60. https://doi.org/10.3897/zookeys.1047.61097
Table S3. Variable loadings for principal components with Eigenvalues greater than 2, from morphometric characters corrected by SVL
FIGURE 1. Petrocosmea funingensis. A in Petrocosmea funingensis (Gesneriaceae): a new species from southeastern Yunnan, China
FIGURE 1. Petrocosmea funingensis. A) Habit; B) Corolla opened showing stamens; C) Calyx; D) Pistil; E–F) Stamen. Drawn by Wen-Hong Lin.
FIGURE 2. Caryodaphnopsis malipoensis. A in A new species of Caryodaphnopsis Airy Shaw (Lauraceae) from southeastern Yunnan, China
FIGURE 2. Caryodaphnopsis malipoensis. A, leaf adaxial surface; B, leaf abaxial surface; C, twig apex showing the pubescent terminal bud; D, flowering branch; E,
FIGURE 1. Caryodaphnopsis malipoensis Bing Liu et Y. Yang. A, a in A new species of Caryodaphnopsis Airy Shaw (Lauraceae) from southeastern Yunnan, China
FIGURE 1. Caryodaphnopsis malipoensis Bing Liu et Y. Yang. A, a flowering branch showing the opposite elliptical leaves and axillary inflorescences; B, twig apex showing the pubescent terminal bud; C, a flower showing the spreading perianth lobes and the stamens; D, outside (left) and inside (right) view of outer perianth lobes showing the triangular shape and pubescence; E, outside (left) and inside (right) view of inner perianth lobes showing the triangular shape and pubescence; F, inside view of a first whorl of stamen showing the pubescent filaments and 4-celled anthers; G, inside view of a second stamen whorl showing pubescent filament and the 4-celled anther; H, outside (left) and inside (right) view of a third whorl stamen showing the pair of glands at the base of the filament; I, outside (left) and inside (right) view of a fourth whorl staminode showing the inner pubescent surface; J, a pistil showing the densely pubescent ovary and short style; K, fruits showing the avocadolike shape, rugged surface sculpturing and the layered pericarp.
FIGURE 3 in A new species of Caryodaphnopsis Airy Shaw (Lauraceae) from southeastern Yunnan, China
FIGURE 3. Fruit structure of Caryodaphnopsis malipoensis and C. tonkinensis. A–D, C. malipoensis; A, fruits showing morphology; B, a fruit longitudinal section; C, pericarp portion showing the 4 layers; D, a seed showing hilum. E–G, C. tonkinensis. E, fruits showing morphology; F, a broken fruit showing the pericarp and the inner seed; G, pericarp portion showing the 4 layers: a1, the outer layer, a, the pulpy layer, b, the sclerotic layer, c, the inner layer. Abbreviations: fa, fruit apex; fb, fruit basal; s, seed; h, hilum.
FIGURE 7 in A new species of Torrent frog (Anura, Ranidae, Amolops) from the Coastal Hills of Southeastern China
FIGURE 7. Comparisons among Amolops teochew sp. nov., congeners in the A. daiyunensis group, and the sympatric A. albispinus. (A) holotype of Amolops teochew sp. nov.; (B) topotype of A. daiyunensis from Mt Daiyun, Fujian; (C) topotype of A. hongkongensis from Tai Mo Shan, Hong Kong; (D) A. hongkongensis from Gutian Nature Reserve, Guangdong; (E) A. albispinus from Mt Dabei, Guangdong; (1) dorsolateral view; (2) ventral hand; (3) ventral foot.
FIGURE 6 in A new species of Torrent frog (Anura, Ranidae, Amolops) from the Coastal Hills of Southeastern China
FIGURE 6. (A) an uncaptured individual of Amolops teochew sp. nov. at a cliff near a steep waterfall in Mt Tongguzhang, Fengshun; (B) an uncaptured individual in a fast-flowing stream in Gutian Town, Shanghang; (C) and (D) the habitats in Mt Fenghuang, Chao'an.
FIGURE 2 in A new species of Torrent frog (Anura, Ranidae, Amolops) from the Coastal Hills of Southeastern China
FIGURE 2. Bayesian inference phylogeny of the Amolops species distributed in southeastern China, with the Bayesian posterior probabilities (BPP) and bootstrap supports for maximum likelihood analysis (BS) all labeled. The number at the branch terminal corresponds to the ID in Table 1 and different colorations for the species correspond to that in Figure 1.
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