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69 results for “Parabuthus”
Figure 1 in A reanalysis of Parabuthus (Scorpiones: Buthidae) phylogeny with descriptions of two new Parabuthus species endemic to the Central Namib gravel plains, Namibia
Figure 1. Map showing the known distributions of Parabuthus glabrimanus sp. nov. (triangles), Parabuthus gracilis Lamoral, 1979 (squares), Parabuthus nanus Lamoral, 1979 (stars) and Parabuthus setiventer sp. nov. (circles) in Namibia and South Africa. Contour interval, 500 m. Major sand systems stippled. Magnified inset shows distributions of P. glabrimanus and P. setiventer in finer detail.
Figures 9–15 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXX. Parabuthus (Buthidae) (Part III), with description of three new species from Somaliland and occurrence of Parabuthus eritreaensis Kovařík, 2003
Figures 9–15: Parabuthus eritreaensis, female. Figure 9. Carapace and tergites I–IV. Figures 10–11. Sternopectinal area and sternites.. Figures 12–15. Right legs I–IV, retrolateral aspect.
Figures 36–48 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXX. Parabuthus (Buthidae) (Part III), with description of three new species from Somaliland and occurrence of Parabuthus eritreaensis Kovařík, 2003
Figures 36–48: Parabuthus dorisae sp. n., male holotype. Figures 36–46. Right pedipalp, chela in dorsal (36), external (37), and ventral (38) views, patella in dorsal (39), external (40), and ventral (41) views, femur and trochanter in internal (42), dorsal (43), and ventral (44) views. Dentate margins of movable (45) and fixed (46) fingers. Trichobothrial pattern indicated in Figures 37– 40 and 42–43 by white circles. Figure 47. Carapace and tergites I–V. Figures 48. Sternopectinal area and sternites.
Figures 94–95 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXX. Parabuthus (Buthidae) (Part III), with description of three new species from Somaliland and occurrence of Parabuthus eritreaensis Kovařík, 2003
Figures 94–95: Parabuthus quincyae sp. n., male holotype. Figure 94. Male holotype in vivo habitus. Figure 95. Locality, Somaliland, vicinity of Huluul.
Figs. 7–9. Parabuthus muelleri Prendini, 2000 in Discovery of the Male of Parabuthus muelleri, and Implications for the Phylogeny of Parabuthus (Scorpiones: Buthidae)
Figs. 7–9. Parabuthus muelleri Prendini, 2000, male (AMNH [AH 3991]), distribution of trichobothria and macrosetae on the dextral pedipalpal chela. 7. Dorsal aspect. 8. Ventral aspect. 9. Internal aspect. Scale bar = 1 mm.
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.
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