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Fig. 2 in Astromesitius, a new genus of Mesitiinae (Hymenoptera, Bethylidae) from the Old World

Fig. 2. Hypopygium of Astromesitius gen. nov. A. A. olavoi gen. et sp. nov. (holotype, QBG) B. A. thionyi gen. et sp. nov. (holotype, UFES 118956) C. A. indistintus (Barbosa & Azevedo, 2011) gen. et comb. nov. (paratype, UFES) D. A. minutissimus (Móczár, 1971) gen. et comb. nov. (holotype, UFES 56528) E. A. quatei (Móczár, 1977) gen. et comb. nov. (holotype, BPBM).

Figures 33-36. Halodromus patellidens from Aden. 33-34 in The Ebo-like running crab spiders in the Old World (Araneae, Philodromidae)

Figures 33-36. Halodromus patellidens from Aden. 33-34 Left male palp (33 ventral, 34 retrolateral) 35 Epigyne, ventral 36 Vulva, dorsal. Scale line = 0.1 mm.

Figures 29-32. Halodromus patellaris from Monastir. 29-30 in The Ebo-like running crab spiders in the Old World (Araneae, Philodromidae)

Figures 29-32. Halodromus patellaris from Monastir. 29-30 Left male palp (29 ventral, 30 retrolateral) 31 Epigyne, ventral 32 Vulva, dorsal. Scale line = 0.1 mm.

Figures 25-28 in The Ebo-like running crab spiders in the Old World (Araneae, Philodromidae)

Figures 25-28. Halodromus gershomi sp. n. from Aden. 25-26 Left male palp (25 ventral, 26 retrolateral) 27 Epigyne, ventral 28 Vulva, dorsal. Scale line = 0.1 mm.

Figures 7-16. 7, 11 Ebo pepinensis from Utah Lake 8, 12 Titanebo parabolis from Utah 9, 15 Halodromus patellaris, from Monastir 10 Philodromus lepidus from Kebili, Tunisia 13 Halodromus patellidens from Kuwait 14 in The Ebo-like running crab spiders in the Old World (Araneae, Philodromidae)

Figures 7-16. 7, 11 Ebo pepinensis from Utah Lake 8, 12 Titanebo parabolis from Utah 9, 15 Halodromus patellaris, from Monastir 10 Philodromus lepidus from Kebili, Tunisia 13 Halodromus patellidens from Kuwait 14 Halodromus barbarae sp. n. from Cartagena 16 Halodromus gershomi sp. n. from Massawa 7-10 Female clypeus and chelicerae, frontal view 11-16 Female cephalothorax, dorsal view. Scale lines = 0.5 mm.

Figures 1-6. 1, 4 Halodromus patellaris from Monastir 2 Ebo pepinensis from Utah Lake 3 Titanebo albocaudatus from Abilene 5-6 Titanebo andreaannae from Tucson 1-3 Left male palp, ventral view 4 Tarsal claws and scopulae 5 in The Ebo-like running crab spiders in the Old World (Araneae, Philodromidae)

Figures 1-6. 1, 4 Halodromus patellaris from Monastir 2 Ebo pepinensis from Utah Lake 3 Titanebo albocaudatus from Abilene 5-6 Titanebo andreaannae from Tucson 1-3 Left male palp, ventral view 4 Tarsal claws and scopulae 5 Epigyne, dorsal view, showing schematic course of the internal ducts (broken black line) and the demarcation between bursa copulatrix and copulatory ducts (white line) 6 Details of receptacula, showing numerous pores in the torus region.

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Figure 1 in Biology and life-table of Typhlodromus (Anthoseius) athenas (Acari: Phytoseiidae) fed with the Old World Date Mite, Oligonychus afrasiaticus (Acari: Tetranychidae)

Figure 1 Population dynamics ofO. afrasiaticus andT. (A.) athenas on date of 'Alig' cultivar at Segdoud, South of Tunisia in 2005 and 2006.

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FIGURE 2. A − C in The first record of the genus Tanaostigma (Hymenoptera: Tanaostigmatidae) in the Old World, with the description of a new species from India

FIGURE 2. A − C, Tanaostigma indica sp. n. ♀: A, dorsal view of body, in part; B, vertex; C, metasoma in dorsal view.

Fig. 29. A in Phyletic Diversification Of The Cormohipparion Occidentale Complex (Mammalia; Perissodactyla, Equidae), Late Miocene, North America, And The Origin Of The Old World Hippotherium Datum

Fig. 29. A, chronogram of species of Cormohipparion showing window for time of origin of H. primigenium-like morphology between the biochrons of C. merriami and C. fricki, the exit of H. primigenium-like morphology at ca. 11.3 Ma, and the age of Cormohipparion sp. from California (illustrated below), thought to be close to the species population that dispersed to the Old World. The?Dispersal barrier? refers to the high sea-level that lowered at about 11.3 MA (Ta3 of Haq et al., 1988; modified by Hardenbol et al., 1998). B, upper cheek tooth dentition of Hippotherium primigenium from Höwenegg, Germany, HLMD 1081. After Sondaar (1961), fig. 21A.

Fig. 16. Cormohipparion johnsoni, F in Phyletic Diversification Of The Cormohipparion Occidentale Complex (Mammalia; Perissodactyla, Equidae), Late Miocene, North America, And The Origin Of The Old World Hippotherium Datum

Fig. 16. Cormohipparion johnsoni, F:AM 71891, Burge Quarry, Burge Member, Valentine Formation, late Barstovian, Nebraska. A, left lateral view of cranium. B, occlusal view of right upper cheek tooth dentition.

Fig. 11 in Phyletic Diversification Of The Cormohipparion Occidentale Complex (Mammalia; Perissodactyla, Equidae), Late Miocene, North America, And The Origin Of The Old World Hippotherium Datum

Fig. 11. Cormohipparion cf. occidentale. F:AM 71872,?Thin Elk Formation, South Dakota, early Clarendonian. A, lateral view of cranium showing tall-crowned upper cheek teeth. B, occlusal view of left upper cheek teeth.

Fig. 13 in Phyletic Diversification Of The Cormohipparion Occidentale Complex (Mammalia; Perissodactyla, Equidae), Late Miocene, North America, And The Origin Of The Old World Hippotherium Datum

Fig. 13. Cormohipparion occidentale. Log-ratio diagrams of cranial dimensions of samples from XMas- Kat, Machaerodus, and Hans Johnson quarries, Merritt Dam Member, Ash Hollow Formation, Nebraska.

Fig. 19. Cormohipparion merriami, AMNH 141219 in Phyletic Diversification Of The Cormohipparion Occidentale Complex (Mammalia; Perissodactyla, Equidae), Late Miocene, North America, And The Origin Of The Old World Hippotherium Datum

Fig. 19. Cormohipparion merriami, AMNH 141219, Burge Quarry, Valentine Formation, Nebraska, late Barstovian. A, left lateral view of cranium. B, occlusal view of upper cheek tooth dentition, drawn by E. L. F.

Fig. 15 in Phyletic Diversification Of The Cormohipparion Occidentale Complex (Mammalia; Perissodactyla, Equidae), Late Miocene, North America, And The Origin Of The Old World Hippotherium Datum

Fig. 15. Log-ratio diagram of cranial dimensions of Cormohipparion matthewi compared with C. occidentale, XMas-Kat quarries, Merritt Dam Member, Ash Hollow Formation, Cherry County, Nebraska.

Fig. 25. Hippotherium and Cormohipparion. A–D in Phyletic Diversification Of The Cormohipparion Occidentale Complex (Mammalia; Perissodactyla, Equidae), Late Miocene, North America, And The Origin Of The Old World Hippotherium Datum

Fig. 25. Hippotherium and Cormohipparion. A–D, Hippotherium sp., Pannonian C?, Mariathal, Austria. E, Hippotherium sp., Pannonian C, Gaiselberg, Austria. F–G, Cormohipparion sp., Punchbowl Formation, LACM 7502, medial Clarendonian, California. A, PIUW 3504/3, LP2, reversed. B, PIUW 3540/97, LP3, reversed. C, PIUW 3540/54, LP4, reversed. D, PIUW 3540/136, RM1. E, NHMW 0024/26, RM2. F, partial palate with right and left P2–M2, occlusal view. Preservation of the specimen apparently masks the complexity of the plis caballin in P4–M2. G, right lateral view of partial palate, showing remnant of posteroventral border of DPOF and the IOF located above the anterior root of P3.

Fig. 7 in Phyletic Diversification Of The Cormohipparion Occidentale Complex (Mammalia; Perissodactyla, Equidae), Late Miocene, North America, And The Origin Of The Old World Hippotherium Datum

Fig. 7. Correlation of rock and faunal units of the Valentine and Ash Hollow formations, Nebraska and South Dakota, modified after Skinner and Johnson (1984: fig. 3).

Fig. 6 in Phyletic Diversification Of The Cormohipparion Occidentale Complex (Mammalia; Perissodactyla, Equidae), Late Miocene, North America, And The Origin Of The Old World Hippotherium Datum

Fig. 6. Diagram of measurements and terminology. A, measurements of mandible. B, symphysis of mandible. C and D, dental terminology. C, upper cheek teeth. D, lower cheek teeth. A and B after Eisenmann et al. (1988). C and D after MacFadden (1984).

Fig. 5 in Phyletic Diversification Of The Cormohipparion Occidentale Complex (Mammalia; Perissodactyla, Equidae), Late Miocene, North America, And The Origin Of The Old World Hippotherium Datum

Fig. 5. Diagram showing location of cranial measurements and features cited in Table 2. A, lateral view. B, close up of facial region, lateral view. A and B after Eisenmann et al. (1988). C, lateral view of Merychippus insignis, F:AM 87001, Echo Quarry (early Barstovian), Nebraska. NMF 5 nasomaxillary fossa. LAF 5 lacrimal fossa. R 5 ridge that separates the NMF from the LAF. IOF 5 infraorbital foramen. After Woodburne (2003: fig. 16.7). D, malar fossa developed below the DPOF but not bounded by definite posterior and ventral rims. E, malar fossa developed below the DPOF, bounded by definite posterior and ventral rims. D and E, Acritohippus isonesus (Kelly, 1995), after Osborn (1918: plate 10, figs. 3, 4; Merychippus isonesus).

Fig. 4 in Phyletic Diversification Of The Cormohipparion Occidentale Complex (Mammalia; Perissodactyla, Equidae), Late Miocene, North America, And The Origin Of The Old World Hippotherium Datum

Fig. 4. Diagram showing location of cranial measurements and cheek tooth measurement methodology. A, dorsal view. B, posterior view. A and B after Eisenmann et al. (1988). C, measurement of length and width of upper cheek teeth and length and width of protocone. D, measurement of MSTHT from base to tip of mesostyle at labial surface of cheek tooth.