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FIGURE 5 in Variability of leaf blade anatomical traits in the Sesleria juncifolia complex (Poaceae) on the Balkan Peninsula

FIGURE 5. Cluster Analysis of populations of S. juncifolia complex (labeled with population acronym shown in Table 1) based on leaf anatomical characters. Color coding of populations reflects the groups (three species) tested in canonical discriminant analysis. Green— populations of S. juncifolia, blue—populations of S. interrupta, red—populations of S. ujhelyii.

FIGURE 3 in Variability of leaf blade anatomical traits in the Sesleria juncifolia complex (Poaceae) on the Balkan Peninsula

FIGURE 3. Typical tiller leaf cross-section of A) Sesleria juncifolia (individual from population from Vojak peak, population ID 2), B) S. interrupta (individual from population from Zaostro, ID 18) and C) S. ujhelyii (individual from population from Ribarići, population ID 14). Most important differential qualitative leaf blade anatomical characters are marked.

FIGURE 2 in Variability of leaf blade anatomical traits in the Sesleria juncifolia complex (Poaceae) on the Balkan Peninsula

FIGURE 2. Tiller leaf cross-section obtained from individual of S. ujhelyii from Sjeverin (left, population ID 13) and S. interrupta from Dobrilovina (right, population ID 16) with measured characters. Bulliform cell (BC), width of the midrib (Rm_W), height of strand/girder in the widest zone of lamina (ScS1_H), height of strand/girder of median vascular bundle (ScSM_H), largest thickness of lamina (T1), distance between the middle and largest thickness of lamina (T2), thickness of midrib (To), height of the largest lateral 1st order vascular bundle (VB1_H), width of the largest lateral 1st order vascular bundle (VB1_W), first order vascular bundle (VB1), third order vascular bundle (VB3), height of the median vascular bundle (VBM_H), width of the median vascular bundle (VBM_W), width of leaf blade (W).

FIGURE 1 in Variability of leaf blade anatomical traits in the Sesleria juncifolia complex (Poaceae) on the Balkan Peninsula

FIGURE 1. Sampled populations of Sesleria juncifolia complex. Population identifiers correspond to Table 1. Color coding of populations reflects the groups (three species) tested in canonical discriminant analysis: green—populations of S. juncifolia, blue—populations of S. interrupta, red—populations of S. ujhelyii.

FIGURE 4 in Variability of leaf blade anatomical traits in the Sesleria juncifolia complex (Poaceae) on the Balkan Peninsula

FIGURE 4. Principal Component Analysis (PCA) based on leaf blade anatomical characters of populations of Sesleria juncifolia complex labeled with population acronym shown in Table 1. Color coding (different shades of blue, red and green) of populations reflects the groups (three species) tested in canonical discriminant analysis. Green—populations of S. juncifolia, blue—populations of S. interrupta, red—populations of S. ujhelyii.

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FIGURE 3 in Edraianthus canescens (Campanulaceae), a new species from the Central Balkan peninsula

FIGURE 3. Distribution of taxa of the Edraianthus graminifolius complex in C. &. S Balkan Peninsula. Arrow indicates stenoendemic range of E. canescens. Country abbreviations: GR: Greece, AL: Albania, MA: Macedonia, BU: Bulgaria, SR: Serbia, BH: Bosnia and Hercegovina.

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FIGURE 2 Edraianthus canescens D in Edraianthus canescens (Campanulaceae), a new species from the Central Balkan peninsula

FIGURE 2 Edraianthus canescens D. Lakušić, Niketić & Stevanović, sp. nov. (from the locus classicus). A. Habitus. B. Inflorescence with involucral bracts. C. Flowers with calyx teeth. D. Rosette leaves. E. Cauline leaves. F. Inflorescence. G.. Capsules with basal lateral pores and axicorns. H. Capsule with axicorn. I. Seed. (photo D. Lakušić).

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FIGURE 1. Edraianthus canescens D in Edraianthus canescens (Campanulaceae), a new species from the Central Balkan peninsula

FIGURE 1. Edraianthus canescens D. Lakušić, Niketić & Stevanović, sp. nov. (from the holotype). A. Habitus. B. Rosette leaf. C. Bracts of flowering capitula. D. Calyx. E. Anther. F. Style. G. Corolla. H. Capsule with axicorn (linedrawing V. Stevanović).

FIGURE 4 in Silene triflora (Bornm.) Bornm. (Caryophyllaceae), a neglected species from the Central Balkans

FIGURE 4. Discriminant analysis (CDA) of morphometric data for 15 populations from the Central Balkan belonging to the S. saxifraga group. Population from the Gorges of Babuna, Pčinja, Pešnica and Treska rivers represent S. triflora (black symbols).

FIGURE 1 in Silene triflora (Bornm.) Bornm. (Caryophyllaceae), a neglected species from the Central Balkans

FIGURE 1. Distribution of sampled populations of Silene saxifraga (squares) and S. triflora (black circles) from the Central Balkans (Cg—Montenegro, Mk—Republic of Macedonia, Sr —Serbia). Black circles without numbers represent literature records only.

FIGURE 3 in Silene triflora (Bornm.) Bornm. (Caryophyllaceae), a neglected species from the Central Balkans

FIGURE 3. Variation in selected morphological characters (stem length, inflorescence length, longest internode length, middle leaf length and number of flowers) for S. saxifraga and S. triflora.

FIGURE 2 in Silene triflora (Bornm.) Bornm. (Caryophyllaceae), a neglected species from the Central Balkans

FIGURE 2. Principal component analysis (PCA) of morphometric data for 15 populations from Central Balkans belonging to S. saxifraga group. Populations from the Gorges of rivers Babuna, Pčinja, Pešnica and Treska represent S. triflora (black symbols).

Figure 6. The maximum-likelihood phylogram for cytochrome oxidase subunit I in A case of biodiversity overestimation in the Balkan Belgrandiella A. J. Wagner, 1927 (Caenogastropoda: Hydrobiidae): molecular divergence not paralleled by high morphological variation

Figure 6. The maximum-likelihood phylogram for cytochrome oxidase subunit I (COI) haplotypes. Bootstrap support and Bayesian posterior probabilities are shown. Normal font indicates reference haplotypes, bold font indicates haplotypes obtained in present study.

Figure 3 in A case of biodiversity overestimation in the Balkan Belgrandiella A. J. Wagner, 1927 (Caenogastropoda: Hydrobiidae): molecular divergence not paralleled by high morphological variation

Figure 3. Shells of Belgrandiella: (a–f) molecular clade A: (a–d) Belgrandiella cf. robusta, spring of river LipsenjŠČica, Cerknica; (e, f) Belgrandiella cf. robusta, Dvorce, Čatež ob Savi; (g) Boleana umbilicata, topotype, spring MoČilnik; (h, i) molecular clade B: Belgrandiella cf. kuesteri, PotoČe; (j–r) molecular clade C: (j) Belgrandiella cf. fontinalis, PotoČe; (k–r) Belgrandiella cf. fontinalis, Babja luknja; (s, t) molecular clade D: Belgrandiella cf. koprivnensis, Izvor Plive 1A, DraganiĆ. Scale bar represents 1 mm.

Figure 2 in A case of biodiversity overestimation in the Balkan Belgrandiella A. J. Wagner, 1927 (Caenogastropoda: Hydrobiidae): molecular divergence not paralleled by high morphological variation

Figure 2. Shells of Belgrandiella (molecular clade A): (a–c) Belgrandiella kusceri, topotype, Rakek; (d, e) Belgrandiella zermanica, topotype, Zrmanja River; (f, g) Belgrandiella krupensis, topotype, Krupa River; (h–j) Belgrandiella cf. fontinalis, Krk Island; (k, l) Belgrandiella robusta, topotype, Veliki Obrh; (m, n) Belgrandiella cf. pageti, KrŠka jama, source of Krka River; (o) Belgrandiella cf. robusta, ŽerovniŠČica; (p–s) Belgrandiella cf. croatica, Rupa na Brodu. Scale bar represents 1 mm.

Figure 1 in A case of biodiversity overestimation in the Balkan Belgrandiella A. J. Wagner, 1927 (Caenogastropoda: Hydrobiidae): molecular divergence not paralleled by high morphological variation

Figure 1. Localities of the studied Belgrandiella and geographic distribution of clades (see Figures 6 and 7).

Figure 5 in A case of biodiversity overestimation in the Balkan Belgrandiella A. J. Wagner, 1927 (Caenogastropoda: Hydrobiidae): molecular divergence not paralleled by high morphological variation

Figure 5. Penes of Belgrandiella: (a) Belgrandiella cf. fontinalis, Babja luknja (molecular clade C); (b–d) Belgrandiella robusta, Obrh, type locality (molecular clade A). Scale bar represents 0.5 mm.

Figure 7. The maximum-likelihood phylogram for H3 in A case of biodiversity overestimation in the Balkan Belgrandiella A. J. Wagner, 1927 (Caenogastropoda: Hydrobiidae): molecular divergence not paralleled by high morphological variation

Figure 7. The maximum-likelihood phylogram for H3 haplotypes. Bootstrap support and Bayesian posterior probabilities are shown.

Figure 4 in A case of biodiversity overestimation in the Balkan Belgrandiella A. J. Wagner, 1927 (Caenogastropoda: Hydrobiidae): molecular divergence not paralleled by high morphological variation

Figure 4. Renal and pallial section of female reproductive organs of Belgrandiella: (a) Belgrandiella fontinalis, Babja luknja (molecular clade C); (b) Belgrandiella robusta, Obrh, type locality (molecular clade A) (bc, bursa copulatrix; cbc, duct of bursa copulatrix; ga, albuminoid gland; gn, nidamental gland; gp, gonoporus; ov, oviduct; ovl, loop of oviduct; rec, rectum; rs, receptaculum seminis). Scale bar represents 1 mm.