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4,585 results for “Scorpion”
FIGURES 23–44 in Three new species of Olivierus (Scorpiones: Buthidae) from Kazakhstan and Uzbekistan
FIGURES 23–44. Olivierus mikhailovi sp. n., paratypes from Kazakhstan, Turkistan Province, Beltau Mts., pedipalp segments. Figures 23–33. Male, pedipalp chela, dorsal (23), external (24), and ventral (25) views. Pedipalp patella, dorsal (26), external (27) and ventral (28) views. Pedipalp femur and trochanter, dorsal (29), internal (30), and ventral (31) views. Movable (32) and fixed (33) fingers dentition. Figures 34–44. Female, pedipalp chela, dorsal (34), external (35), and ventral (36) views. Pedipalp patella, dorsal (37), external (38) and ventral (39) views. Pedipalp femur and trochanter, dorsal (40), internal (41), and ventral (42) views. Movable (43) and fixed (44) fingers dentition. The trichobothrial pattern is indicated in Figures 35–38, 40–41 by white circles.
FIGURES 1–4 in Three new species of Olivierus (Scorpiones: Buthidae) from Kazakhstan and Uzbekistan
FIGURES 1–4. Olivierus mikhailovi sp. n., paratypes from Kazakhstan, Turkistan Province, Beltau Mts. 1–2. Male, dorsal (1) and ventral (2) views. 3–4. Female, dorsal (3) and ventral (4) views. Scale bar: 10 mm.
FIGURES 86–91 in Three new species of Olivierus (Scorpiones: Buthidae) from Kazakhstan and Uzbekistan
FIGURES 86–91. Olivierus voldemari sp. n., female holotype. Figures 86–87. Dorsal (86) and ventral (87) views. Figures 88–91. Telson lateral (88) and metasoma and telson, lateral (89), dorsal (90), and ventral (91) views. Scale bar: 10 mm (86–87, 89–91).
FIGURES 64–85 in Three new species of Olivierus (Scorpiones: Buthidae) from Kazakhstan and Uzbekistan
FIGURES 64–85. Olivierus tarabaevi sp. n., pedipalp segments. Figures 64–74. Male paratype, pedipalp chela, dorsal (64), external (65), and ventral (66) views. Pedipalp patella, dorsal (67), external (68) and ventral (69) views. Pedipalp femur and trochanter, dorsal (70), internal (71), and ventral (72) views. Movable (73) and fixed (74) fingers dentition. Figures 75–85. Female holotype, pedipalp chela, dorsal (75), external (76), and ventral (77) views. Pedipalp patella, dorsal (78), external (79) and ventral (80) views. Pedipalp femur and trochanter, dorsal (81), internal (82), and ventral (83) views. Movable (84) and fixed (85) fingers dentition. The trichobothrial pattern is indicated in Figures 76–79, 81–82 by white circles.
Figure 4 in Novel trophic interaction: the scuttle fly Megaselia scalaris (Diptera: Phoridae) is a facultative parasitoid of the desert scorpion Mesobuthus eupeus mongolicus (Scorpiones: Buthidae)
Figure 4. Suitable distributional areas for the scuttle fly Megaselia scalaris and the scorpion Mesobuthus eupeus mongolicus predicted with ecological niche modeling. The map shows the climatically suitable range for the scuttle fly under the minimum training presence threshold which included all known training occurrence points and under 10 percentile training presence threshold in which 10% of the occurrence points used in training models was omitted. Distribution for M. eupeus mongolicus was generated from Shi, Liang, et al. (2015). The crossed circle indicates the place where parasitised scorpions were collected.
Figure 3 in Novel trophic interaction: the scuttle fly Megaselia scalaris (Diptera: Phoridae) is a facultative parasitoid of the desert scorpion Mesobuthus eupeus mongolicus (Scorpiones: Buthidae)
Figure 3. Genetic divergences among the haplotypes of Megaselia scalaris are shown as NeighborNet based on p-distances of mtCOI sequences. Circle sizes are proportional to the number of isolates sharing the haplotypes. Isolates from the scorpion Mesobuthus eupeus mongolicus are all included in Hap8.
Figure 1 in Novel trophic interaction: the scuttle fly Megaselia scalaris (Diptera: Phoridae) is a facultative parasitoid of the desert scorpion Mesobuthus eupeus mongolicus (Scorpiones: Buthidae)
Figure 1. Scorpion, Mesobuthus eupeus mongolicus (a) and its parasitoid scuttle fly, Megaselia scalaris (b–e): (a) a female scorpion; (b) larvae of fly emerging from the genital operculum of scorpion; (c) fly larva; (d) fly pupa; (e) a male fly.
Figure 5 in Locomotory activity and orientation of Mesobuthus gibbosus (Scorpiones: Buthidae) in central Aegean Archipelago
Figure 5. Rose diagram showing the direction of movement of the studied population of Mesobuthus gibbosus in the study site. Frequency is represented by the area of each wedge. The thick black line represents the dry-stone wall.
Figure 4 in Locomotory activity and orientation of Mesobuthus gibbosus (Scorpiones: Buthidae) in central Aegean Archipelago
Figure 4. Nightly activity records of Mesobuthus gibbosus during its circadian cycle in relation to moon phase and the exact time of sunrise/sunset and the end/beginning of astronomical twilight.
Figure 3 in Locomotory activity and orientation of Mesobuthus gibbosus (Scorpiones: Buthidae) in central Aegean Archipelago
Figure 3. The average fraction of the moon visible (± SD) during the time of capture comparatively for scorpions found hidden and those found in the open field.
Figure 1 in Locomotory activity and orientation of Mesobuthus gibbosus (Scorpiones: Buthidae) in central Aegean Archipelago
Figure 1. Distribution of Mesobuthus gibbosus individuals recaptured in the days elapsed after previous capture.
Figure 3 in Phylogenetic relationships of Mesobuthus eupeus (C.L. Koch, 1839) inferred from COI sequences (Scorpiones: Buthidae)
Figure 3. Principal component analysis of Mesobuthus eupeus and Mesobuthus caucasicus based on morphological ratios. (A) and (B) plot positions of the species, respectively, with respect to the first and second components and with respect to the first and third components (see text). Mesobuthus eupeus and M. caucasicus are encircled according to species identification in phylogenetic tree shown in Figure 2:, M. eupeus;, M. caucasicus.
Figure 2 in Phylogenetic relationships of Mesobuthus eupeus (C.L. Koch, 1839) inferred from COI sequences (Scorpiones: Buthidae)
Figure 2. Fifty per cent majority rule consensus tree resulting from maximum likelihood analysis. Numbers below branches indicate the posterior probabilities of the nodes in the Bayesian inference analysis. Numbers above branches are the bootstrap values of the nodes in the maximum likelihood analysis. The estimated separation time for calibration point (± standard deviations) is also displayed. The geographic distributions of inferred clades are shown on the embedded map.
Figure 5 in Phylogenetic relationships of Mesobuthus eupeus (C.L. Koch, 1839) inferred from COI sequences (Scorpiones: Buthidae)
Figure 5. Canonical discriminant analysis of Mesobuthus eupeus and Mesobuthus caucasicus species based on morphological ratios. Mesobuthus eupeus and M. caucasicus are grouped according to species identification shown in Figure 2:, M. eupeus clade A;, M. eupeus clade B;, M. caucasicus;, group centroid.
Figure 4 in Phylogenetic relationships of Mesobuthus eupeus (C.L. Koch, 1839) inferred from COI sequences (Scorpiones: Buthidae)
Figure 4. Principal component analysis of Mesobuthus eupeus based on morphological ratios. The specimens are plotted with respect to first and second components (see text). Mesobuthus eupeus specimens are encircled within clades according to phylogenetic tree shown in Figure 2:
Figure 8. Correspondence analysis plots. M1–M4 in The foraging activity of Mesobuthus gibbosus (Scorpiones: Buthidae) in central and south Aegean archipelago
Figure 8. Correspondence analysis plots. M1–M4: moon phase classes from minimum (M1) to maximum (M4); Al1–Al4: moon altitude classes; Az1–Az4: moon azimuth classes; sw, sitand-wait; dk, doorkeeping; C, Crete; K, Koufonisi.
Figure 4 in The foraging activity of Mesobuthus gibbosus (Scorpiones: Buthidae) in central and south Aegean archipelago
Figure 4. Comparative diagrams of average wind speed measurements (¡S.D.) in the open field and inside bushes in Crete (C) and Koufonisi (K) per sampling hour.
Figure 1 in The foraging activity of Mesobuthus gibbosus (Scorpiones: Buthidae) in central and south Aegean archipelago
Figure 1. Maps of the study sites. In order to maintain uniformity in sampling, the study area was divided into line transects (represented as arrows) each approximately 7 m apart.
Figure 7. Correspondence analysis plots. A1–A4 in The foraging activity of Mesobuthus gibbosus (Scorpiones: Buthidae) in central and south Aegean archipelago
Figure 7. Correspondence analysis plots. A1–A4: air temperature classes from minimum (A1) to maximum (A4); H1–H4: air relative humidity classes; S1–S4: soil temperature classes; W1– W4: wind speed classes; M1–M4: moon phase classes; sw, sit-and-wait; dk, doorkeeping; C, Crete; K, Koufonisi.
Figure 6 in The foraging activity of Mesobuthus gibbosus (Scorpiones: Buthidae) in central and south Aegean archipelago
Figure 6. The distribution of the body lengths of the observed foraging individuals at both study sites.
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