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FIGURE 10 in Molecular and morphological evidence for short range endemism in the Kinnecaris solitaria complex (Copepoda: Parastenocarididae), with descriptions of seven new species 3026

FIGURE 10. Kinnecaris esbe sp. nov., paratype female: A, antennula, dorsal view; B, exopod of antenna, lateral view; C, second swimming leg, anterior view; D, third swimming leg, anterior view; E, fourth swimming leg, anterior view. Scale 50 µm for all figures. Arrow pointing smaller praecoxa and coxa of third swimming leg when compared to previous species.

FIGURE 9 in Molecular and morphological evidence for short range endemism in the Kinnecaris solitaria complex (Copepoda: Parastenocarididae), with descriptions of seven new species 3026

FIGURE 9. Kinnecaris esbe sp. nov., paratype female: A, habitus, dorsal view; B, urosome, lateral view; C, urosome, ventral view. Inset showing cuticular pits and fine ornamentation of urosome. Arrows pointing additional rows of large spinules on genital double-somite (B), extremely elongated caudal rami, and fewer large spinules on abdominal somites when compared to previous species (C).

FIGURE 5 in Molecular and morphological evidence for short range endemism in the Kinnecaris solitaria complex (Copepoda: Parastenocarididae), with descriptions of seven new species 3026

FIGURE 5. Kinnecaris barrambie sp. nov., SEM photographs, A-D, holotype male; E, allotype female: A, habitus lateral view; B, fifth and sixth legs, lateral view; C, anal somite and caudal rami, lateral view; D, distal part of third swimming legs, lateral view; E, anal somite and caudal rami, ventral view.

FIGURE 1 in Redescription of the tadpole of Macrogenioglottus alipioi (Anura: Cycloramphidae), a rare and endemic species of the Brazilian Atlantic Forest

FIGURE 1. Tadpole of Macrogenioglottus alipioi at stage 35 (Gosner 1960) (MUFAL 8433). (A) Lateral, (B) dorsal, and (C) ventral views (scale = 10 mm); (D) oral disc (scale = 1 mm). (E) Newly metamorphosed juvenile of M. alipioi (MUFAL 2770; SVL 17.8 mm).

FIGURE 5 in The anatomical, palynological and micromorphological aspects of three endemic Bellevalia species (Asparagaceae) in Turkey and their taxonomic importance

FIGURE 5. SEM micrographs of seeds of the studied Bellevalia taxa. a–c. B. gracilis; d–f. B. malatyaensis; g–i. B. vuralii.

FIGURE 5 in Reinstatement of Aloe labiaflava (Asphodelaceae subfam. Alooideae), a distinctive species of maculate aloe endemic to the western Mpumalanga province of South Africa

FIGURE 5. The apical ⅓ of the flowers of A. labiaflava are whitish yellow to golden yellow, as here. Photograph: Gideon F. Smith.

FIGURE 7 in Reinstatement of Aloe labiaflava (Asphodelaceae subfam. Alooideae), a distinctive species of maculate aloe endemic to the western Mpumalanga province of South Africa

FIGURE 7. Coloured plate, dated "1.9.1935" and held at Herb. PRE, of which the corresponding components (habit, bud and flower, leaf, and frontal view of flower mouth) are identical to those in the illustration in Groenewald (1936: unnumbered page opposite p. 58).

FIGURE 2 in Reinstatement of Aloe labiaflava (Asphodelaceae subfam. Alooideae), a distinctive species of maculate aloe endemic to the western Mpumalanga province of South Africa

FIGURE 2. The generally pale flesh-pink- to dull brick-red-flowered Aloe davyana var. davyana co-occurs with A. labiaflava at the western Mpumalanga location to which the latter is restricted (see text for a discussion). Photograph: Gideon F. Smith.

FIGURE 1 in Reinstatement of Aloe labiaflava (Asphodelaceae subfam. Alooideae), a distinctive species of maculate aloe endemic to the western Mpumalanga province of South Africa

FIGURE 1. Aloe labiaflava is a distinctive maculate aloe that usually grows on rocky outcrops as solitary rosettes in sparse to mediumdense grassland. Note that the rosettes almost invariably produce only a single, often unbranched inflorescence per flowering season. Photograph: Gideon F. Smith.

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FIGURE 1 in Rayenia malalcurensis (Escalloniaceae), a new genus and species endemic to Central Chile

FIGURE 1. Distribution maps of Rayenia malalcurensis (A, B, C). A. Chile. B. Ñuble Region with provincial limits (grey lines). C. Sites of R. malalcurensis (red stars), contour lines every 200 m elevation.

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FIGURE 4. Rayenia malalcurensis. A. Whole cushion. B, C. Rosettes and leaves. D, E, F. Flowers. G. Immature fruit. H in Rayenia malalcurensis (Escalloniaceae), a new genus and species endemic to Central Chile

FIGURE 4. Rayenia malalcurensis. A. Whole cushion. B, C. Rosettes and leaves. D, E, F. Flowers. G. Immature fruit. H. Mature fruit. Photographed by Kora Menegoz and Alejandro E. Villarroel.

Figure 9. Parabuthus gracilis Lamoral, 1979 in A reanalysis of Parabuthus (Scorpiones: Buthidae) phylogeny with descriptions of two new Parabuthus species endemic to the Central Namib gravel plains, Namibia

Figure 9. Parabuthus gracilis Lamoral, 1979 (A) and Parabuthus glabrimanus sp. nov. (B–E), dextral pedipalp chela, illustrating trichobothrial distribution. A, ♂ [AMNH (AH 4397)], external aspect. B, holotype ♂ (SMN 2901), external aspect. C–E, paratype ♀ (AMNH), external (C), ventral (D), and internal (E) aspects. Scale bar = 1 mm.

Figure 6 in A reanalysis of Parabuthus (Scorpiones: Buthidae) phylogeny with descriptions of two new Parabuthus species endemic to the Central Namib gravel plains, Namibia

Figure 6. Parabuthus glabrimanus sp. nov. (A), Parabuthus gracilis Lamoral, 1979 (B), Parabuthus nanus Lamoral, 1979 (C) and Parabuthus setiventer sp. nov. (D), sternites III–VII, ventral aspect. A, ♂ [AMNH (AH 2164)]. B–D, ♂ (AMNH). Scale bars = 2 mm.

Figure 4. Alternative topologies for node B in A reanalysis of Parabuthus (Scorpiones: Buthidae) phylogeny with descriptions of two new Parabuthus species endemic to the Central Namib gravel plains, Namibia

Figure 4. Alternative topologies for node B (Fig. 2) retrieved by analyses with equal weights and implied weights under k = 3–6 (A) and with implied weights under k = 1 and 2 (B, C). See Table 2 for details.

Figure 2. See Table 2 in A reanalysis of Parabuthus (Scorpiones: Buthidae) phylogeny with descriptions of two new Parabuthus species endemic to the Central Namib gravel plains, Namibia

Figure 2. See Table 2 for details. The optimal tree retrieved by analyses with equal weights and implied weights under k = 3–6 (Table 2). This topology corresponds to the majority rule (> 50%) consensus of most parsimonious trees (MPTs) obtained by seven analyses in which weighting regime was varied; frequency percentages for nodes that collapsed in the strict consensus of the MPTs obtained by the seven analyses are indicated to the right of relevant nodes. Zero-length branches are collapsed. Solid bars indicate uniquely derived apomorphic character states, whereas empty bars indicate parallel derivations of apomorphic states under accelerated transformation (ACCTRAN) optimization. The number above each bar gives the character number, whereas the number below gives the character state. Branch support values are circled at nodes. Refer to Appendix for character descriptions. The East African species are indicated with asterisks. Alternative topologies for nodes A and B shown in Figures 3 and 4 respectively.

Figure 2 in A new genus and species of planthopper from Seychelles endemic palm forest (Hemiptera: Fulgoromorpha: Derbidae)

Figure 2. Morphological features of Salaziella praslinensis gen. & sp. nov. (paratype female RMBH Sph0919). (a) Head (frontal view). (b) Head, pronotum, and mesonotum (dorsal view). (c) Head, pronotum, and mesonotum (lateral view). (d) Hind tibia and tarsus (lateral view). (Photos: Elizaveta A. Spitsyna).

opennotspecifiedOct 2010View details →

Figure 8 in Three new species of Callulina (Amphibia: Anura: Brevicipitidae) highlight local endemism and conservation plight of Africa's Eastern Arc forests

Figure 8. Maximum-likelihood phylogenies of Callulina, with new species marked in light-grey boxes, and with holotypes marked in dark grey. Letters above branches refer to bootstrap results (MP, ML) and Bayesian posterior probabilities. Below branches Bremer support values and Templeton test results are given, either rejected (–) or accepted (+), with 0.05 as the cut-off point.

opennotspecifiedOct 2010View details →

Figure 1 in Three new species of Callulina (Amphibia: Anura: Brevicipitidae) highlight local endemism and conservation plight of Africa's Eastern Arc forests

Figure 1. Map of the Eastern Arc Mountains of Tanzania showing the distribution of Callulina. Inset map (bottom left) showing the distribution of South Pare species Callulina stanleyi sp. nov. (elevational range of 1200–1600 m), and Callulina shengena sp. nov. (elevational range of 1920–2100 m).

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FIGURE 1 in A new species of Crassula (Crassulaceae subfam. Crassuloideae), C. stylesii, from the Maputaland-Pondoland Region of Endemism in KwaZulu-Natal, South Africa

FIGURE 1. Crassula stylesii from KwaNyuswa, KwaZulu-Natal province, South Africa. A. Inflorescence with white flowers. B. Stem section with leaves distinctly 4-ranked in young plants, dorso-lateral view. C. Habit. D. Shoots with uniformly hairy leaves becoming strongly purple-infused when stressed. E. Habitat at type locality. F. David Styles (1968–) for whom the species is named. Scale bars: A: 15 mm; B: 17 mm; C: 15 cm; D: 20 mm. Photographs by the authors (A–D, F) and D.G.A. Styles (E).