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Supplementary material 1 from: Xiao QY, Tan JB, Hu HY, Zhou SD, He XJ (2017) Semenovia gyirongensis (Apiaceae), a new species from Xizang, China. PhytoKeys 82: 57-72. https://doi.org/10.3897/phytokeys.82.13010

Supporting Information : Explanation note: The following Supporting Information is available for this article: Figure S1–S3 and Tables S1–S2.

FIGURE 2 in Semenovia torilifolia is conspecific with S. malcolmii (Apiaceae) based on morphology and molecular data

FIGURE 2. Primary pinnae of basal leaves in Semenovia malcolmii, showing variation of terminal leaf lobes shape. Scale bars = 5 mm.

FIGURE 1. A in Semenovia torilifolia is conspecific with S. malcolmii (Apiaceae) based on morphology and molecular data

FIGURE 1. A map of the sampling sites used in this study. Purple and gray dots indicate that our collecting samples were identified as S. torilifolia and S. malcolmii based on the type specimens and protologues, respectively.

FIGURE 5 in Semenovia torilifolia is conspecific with S. malcolmii (Apiaceae) based on morphology and molecular data

FIGURE 5. Phylogenetic tree obtained from Bayesian inference of the combined ITS and ETS sequences from Apiaceae tribe Tordylieae and outgroups, onto which two color dots have been mapped. This tree was highly consistent with those inferred using maximum parsimony. The names of the major clades are based on previous studies (Logacheva et al. 2010). The BS and PP values are shown for the clades (BS/PP) (only those greater than 50% and 0.5 are shown).

FIGURE 4 in Semenovia torilifolia is conspecific with S. malcolmii (Apiaceae) based on morphology and molecular data

FIGURE 4.The dorsal (A) and commissural view (B) of mericarp in Semenovia malcolmii, showing the variation of fruits shape and mericarp vittae length. Scale bars = 1 mm.

FIGURE 3 in Semenovia torilifolia is conspecific with S. malcolmii (Apiaceae) based on morphology and molecular data

FIGURE 3. Variation of petals color, the marginal petals size and bracteoles shape in Semenovia malcolmii: (A) the adaxial and (B) abaxial sides of umbellets. Scale bars = 5 mm.

FIGURE 3 in The end of the long road: Iranian endemic Seseli elbursense (Apiaceae) has taken its place in the genus Semenovia

FIGURE 3. Trachydium eriocarpum, lectotype (B 100367270). Courtesy of the Botanischer Garten und Botanisches Museum Berlin- Dahlem.

FIGURE 6 in The end of the long road: Iranian endemic Seseli elbursense (Apiaceae) has taken its place in the genus Semenovia

FIGURE 6. Bayesian analysis phylogenetic tree of nrITS/ETS nucleotide sequences. Posterior probability values and bootstrap values of maximum parsimony analysis are shown.

FIGURE 5 in The end of the long road: Iranian endemic Seseli elbursense (Apiaceae) has taken its place in the genus Semenovia

FIGURE 5. Bayesian analysis phylogenetic tree of nrITS nucleotide sequences. Posterior probability values and bootstrap values of maximum parsimony analysis are shown.

FIGURE 4 in The end of the long road: Iranian endemic Seseli elbursense (Apiaceae) has taken its place in the genus Semenovia

FIGURE 4. Semenovia subscaposa, holotype (W 1958-0003384). Courtesy of the Naturhistorisches Museum Wien.

FIGURE 4 in Morphological and phylogenetic evidence for the transfer of the monotypic genus Tordyliopsis to Semenovia (Apiaceae)

FIGURE 4. Mericarps of Tordyliopsis brunonis. A. mericarps in different development stages; B. ventral face of a mature mericarp; C. cross-section of a mature mericarp.

FIGURE 2 in Morphological and phylogenetic evidence for the transfer of the monotypic genus Tordyliopsis to Semenovia (Apiaceae)

FIGURE 2. Bayesian tree of Tordyliopsis and its allies based on 79 coding sequences from complete plastid genomes. The statistical support values for each branch are indicated by the maximum likelihood bootstrap supports (BS) and the Bayesian posterior probability (PP) values, which are listed above or below the branches, respectively.

FIGURE 3 in Morphological and phylogenetic evidence for the transfer of the monotypic genus Tordyliopsis to Semenovia (Apiaceae)

FIGURE 3. Habit and morphology of Tordyliopsis brunonis. A. habit; B. umbels; C. petals; D. bracts and bracteoles; E. fruits.

Figure 2 from: Xiao QY, Tan JB, Hu HY, Zhou SD, He XJ (2017) Semenovia gyirongensis (Apiaceae), a new species from Xizang, China. PhytoKeys 82: 57-72. https://doi.org/10.3897/phytokeys.82.13010

Figure 2 - Diagnostic morphological characters of Semenovia gyirongensis (A1–A6) in comparison to the similar species Semenovia malcolmii (B1–B6) A1–B1 Habitat A2 Oblong minute bracts, apex obtuse-rounded or cuneate B2 linear to narrowly ovate bracts, apex acute A3 narrowly ovate to ovate ultimate leaf lobes B3 linear to narrowly long-ovate ultimate leaf lobes A4 Long-branched underground caudex with distinct nodes B4 Short-branched overground or emergent caudex A5 Cylindric and much-branched root B5 Fusiform and unbranched root A6 Ellipsoidal pollen grains B6 Equatorially constricted pollen grains.

Figure 1 from: Xiao QY, Tan JB, Hu HY, Zhou SD, He XJ (2017) Semenovia gyirongensis (Apiaceae), a new species from Xizang, China. PhytoKeys 82: 57-72. https://doi.org/10.3897/phytokeys.82.13010

Figure 1 - Semenovia gyirongensis A–B Habitat C Abaxial surface of primary pinnae D Basal leaf sheaths E Middle-upper cauline leaf sheaths F Rays G Adaxial surface of primary pinnae, showing hairs H Compound umbel I Umbellule J Bracts K Calyx teeth and stylopod L Infructescence M Dorsal side of mericarp N Commissural side of mericarp O Cerebroid ornamentation on equatorial plane of pollen grain P Tricolporate Q Rounded pollen polar ends.

Figure 3 from: Xiao QY, Tan JB, Hu HY, Zhou SD, He XJ (2017) Semenovia gyirongensis (Apiaceae), a new species from Xizang, China. PhytoKeys 82: 57-72. https://doi.org/10.3897/phytokeys.82.13010

Figure 3 - Phylogenetic tree inferred from tribe Tordylieae and outgroups of combined ITS/ETS dataset based on Bayesian inference (BI) method. The names of the major clades follow the study of Logacheva et al. (2010). Support values only those greater than 50% ML-BS, 50% MP-BS and 0.5 BI-PP are shown along the branches. Numbers on the branches indicated ML-BS/ MP-BS/ BI-PP, respectively. Asterisks denoted (*) the values of 100/100/1.00 for ML-BS/ MP-BS/ BI-PP. Dshes (-) indicated ML-BS and MP-BS values <50%.

Figure 4 from: Xiao QY, Tan JB, Hu HY, Zhou SD, He XJ (2017) Semenovia gyirongensis (Apiaceae), a new species from Xizang, China. PhytoKeys 82: 57-72. https://doi.org/10.3897/phytokeys.82.13010

Figure 4 - Illustrations of Semenovia gyirongensis (from the holotype) A Habit B Basal leaf C Compound umbel D Flower E Dorsal surface of mericarp F Commissural surface of mericarp.

FIGURE 2 in The end of the long road: Iranian endemic Seseli elbursense (Apiaceae) has taken its place in the genus Semenovia

FIGURE 2. Representative specimen of Seseli elbursense (MW 0757073).

FIGURE 1 in The end of the long road: Iranian endemic Seseli elbursense (Apiaceae) has taken its place in the genus Semenovia

FIGURE 1. Representative specimen of Seseli elbursense (MW 0757074).

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FIGURE 1 in Morphological and phylogenetic evidence for the transfer of the monotypic genus Tordyliopsis to Semenovia (Apiaceae)

FIGURE 1. Bayesian tree of Tordyliopsis and its allies based on ITS sequences. Values on each node indicate ML bootstrap probabilities/ Bayesian posterior probabilities.