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1,212 results for “Old World”
Figs 49–55 in A Review Of The Old World Species Of Ceroptera Macquart, 1835 (Diptera, Sphaeroceridae)
Figs 49–55. Ceroptera armata sp. n., male: 49 = left mid tibia, 50 = sternite 5, ventral view, 51 = synsternite 6–8, ventral view, 52 = postgonite, broadest extension (lateral view), 53 = surstylus, broadest (sublateral) view, 54 = phallus and phallapodeme, lateral view, 55 = left cercus and surstylus with left half of subepandrial sclerite (mostly covered), caudal view. Scales: 0.2 mm for Fig. 49 and Figs 50–51, 54, respectively, 0.1 mm for Figs 52–53, 55.
FIGURE 2 in Morphological and genetic diversification of Old-World marbled newts, with the description of a new and 'not-at-all-cryptic' subspecies from the Iberian Peninsula (Triturus, Salamandridae)
FIGURE 2 The distribution of two species of marbled newts over the western part of the Iberian Peninsula, as inferred from the morphological character Nlinks. Triturus marmoratus is shown in two shades of blue, T. pygmaeus in two shades of red and four localities with both species are shown in grey (see colour legend). The spatial extrapolation does not exceed ca. 50 km. Note that southern Iberian populations are all T. pygmaeus, irrespective of high (cluster C1), low (C2), or bimodal Nlink counts (Doñana National Park). Populations that were studied morphometrically are highlighted by a box. The type locality for T. pygmaeus lusitanicus ssp. nov. is Granja, Portugal and is marked by an asterisk.
FIGURE 4 in Morphological and genetic diversification of Old-World marbled newts, with the description of a new and 'not-at-all-cryptic' subspecies from the Iberian Peninsula (Triturus, Salamandridae)
FIGURE 4 Morphological and genetic variation in Triturus pygmaeus from in and around Doñana National Park (DNP). A – histograms of Nlink counts for four population groups with, from top to bottom: southwestern cluster of T. pygmaeus (localities 65, 436, 438 and 1004 in the south of Portugal, together marked C1 in fig. 2), populations in the northern section of DNP (ER, locality 1005 and BS, locality 1006), population in the southern section of DNP (locality 271) and the Betic cluster of T. pygmaeus (localities 270, 463, 465 and 1003 in the very south of Spain, together marked C2 in fig. 1). Exceptionally, the northern Doñana museum material contains 15 juvenile specimens (open bars) along with three adults (shaded bars). B – geographical cline in microsatellite genetic variation. The horizontal axis shows 'Distance from the Guadalquivir River' in km and the vertical axis presents Structure Q-scores. The solid round symbols represent populations and the grey area shows the 95% credibility interval. The Structure Q-scores were extracted from a published figure (Albert & García-Navas, 2022: Figure 4) and are unavoidably imprecise. The position of the 'Torre Carbonero', a cultural landmark at the Doñana beach, is shown by an arrow (TC). Three populations with morphological data available, that can be associated to the transect are El Rocío (arrow marked ER) and the biological station (BS) in northern Doñana and Zacallón C. de los Junqueros in southern Doñana (arrow marked 271). For details, see table 1 and supplementary table S1.
FIGURE 3 in Morphological and genetic diversification of Old-World marbled newts, with the description of a new and 'not-at-all-cryptic' subspecies from the Iberian Peninsula (Triturus, Salamandridae)
FIGURE 3 Nine marbled newts from three (sub)species each in dorsal and ventral view. Link counts for the left and right side of the body are given in parentheses. Top row – Triturus marmoratus from Jublains, France; left male (3, 2) and right female (1, 1). Middle row – T. pygmaeus lusitanicus ssp. nov. from Cardeña, Spain; from left to right female (2, 4), male (4, 3) and male (4, 5). Bottom row – T. p. pygmaeus from Salinas, Spain; from left to right male (2, 1), male (1, 2) male (2,0) and female (3, 1). Note that the colour pattern in T. marmoratus and T. p. pygmaeus is horizontally banded whereas in T. p. lusitanicus ssp. nov. it is reticulated. PHOTOGRAPHY L. A. VAN DER LAAN
Fig. 8 in Empidoid flies from Cabo Verde (Diptera, Empidoidea, Dolichopodidae and Hybotidae) are not only composed of Old World tropical species
Fig. 8. Crossopalpus complicatus sp. nov., male holotype, terminalia (leg. P. Grootaert and I. Van de Velde, RBINS). A. Right surstyli. B. Lateral view of right epandrial lamella. C. Dorsal view of epandrium, with detail of left surstyli. D. Tip of right surstylus from inside. Scales: 0.1 mm.
Fig. 1 in Empidoid flies from Cabo Verde (Diptera, Empidoidea, Dolichopodidae and Hybotidae) are not only composed of Old World tropical species
Fig. 1. Aphrosylus salensis sp. nov., male holotype, habitus (leg. P. Grootaert and I. Van de Velde, RBINS).
Fig. 2 in Empidoid flies from Cabo Verde (Diptera, Empidoidea, Dolichopodidae and Hybotidae) are not only composed of Old World tropical species
Fig. 2. Aphrosylus salensis sp. nov., male holotype, terminalia. A. Epandrium, lateral view. B. Cerci, dorsal view. C. Ventral surstylus, lateral view. D. Ventral view of epandrium, below the epandrial lobes. E. Ventral view of epandrium. Scales: 0.1 mm.
Fig. 5 in Empidoid flies from Cabo Verde (Diptera, Empidoidea, Dolichopodidae and Hybotidae) are not only composed of Old World tropical species
Fig. 5. Crossopalpus salensis sp. nov., male paratype, terminalia (leg. P. Grootaert and I. Van de Velde, RBINS). A. Right epandrial lamella with right surstylus. B. Dorsal view of epandrium. C. Tip of right surstylus, with left surstyli below. D. Left surstyli, lateral view. Scales: 0.1 mm.
Fig. 7 in Empidoid flies from Cabo Verde (Diptera, Empidoidea, Dolichopodidae and Hybotidae) are not only composed of Old World tropical species
Fig. 7. Crossopalpus complicatus sp. nov., male holotype, habitus (leg. P. Grootaert and I. Van de Velde, RBINS).
Fig. 6 in Empidoid flies from Cabo Verde (Diptera, Empidoidea, Dolichopodidae and Hybotidae) are not only composed of Old World tropical species
Fig. 6. View of the sebkha to the northwest of Santa Maria (Sal), where Crossopalpus salensis sp. nov. was recorded.
Fig. 4 in Empidoid flies from Cabo Verde (Diptera, Empidoidea, Dolichopodidae and Hybotidae) are not only composed of Old World tropical species
Fig. 4. Crossopalpus salensis sp. nov., male holotype, habitus (leg. P. Grootaert and I. Van de Velde, RBINS).
Fig. 3 in Empidoid flies from Cabo Verde (Diptera, Empidoidea, Dolichopodidae and Hybotidae) are not only composed of Old World tropical species
Fig. 3. Tachytrechus tessellatus (Macquart, 1842), male, habitus (leg. P. Grootaert and I. Van de Velde, RBINS; photo credit Rene Ong). Scale: 1 mm.
Figures 1–3 in A new species of Mermiglossa from Kenya, with comments on the arrangement of Old World Panurginae (Hymenoptera: Andrenidae)
Figures 1–3. Female holotype of Mermiglossa voicola, new species. 1. Lateral habitus. 2. Dorsal habitus. 3. Facial aspect.
Fig. 6 in The evolution of early Spermophilus in eastern Europe and the antiquity of the Old World ground squirrels
Fig. 6. Ground squirrel Spermophilus praecox sp. nov. from the late Pliocene and Early Pleistocene of southern Ukraine: Kryzhanovka 2 (A, J), Kotlovina 2 (E, F, K, L, Q, R), Kotlovina 3 (G, M, S), Yuzhny (B, N, T, U), Morskoy (C, D, H, I, V, W); upper cheek teeth (A–D, P3; E–I, P4; J–P, M1–M2; Q–W, M3), in occlusal views. A. ZIN 105160/1. B. GIN 1166/1. C. NMNHU-P MoT-2. D. NMNHU-P MoT-4. E. NMNHU-P 41-5588. F. NMNHU-P 41-5589. G. NMNHU-P 41-5611. H. NMNHU-P MoT-6. I. NMNHU-P MoT-10. J. ZIN 105160/5. K. NMNHU-P 41-5598 (holotype). L. NMNHU-P 41-5599. M. NMNHU-P 41-5613. N. GIN 1166/4. O. NMNHU-P MoT-14. P. NMNHU-P MoT-16. Q. NMNHU-P 41-5601. R. NMNHU-P 41-5602. S. NMNHU-P 41-5616. T. GIN 1166/11. U. GIN 1166/12. V. NMNHU-P MoT-31. W. NMNHU-P MoT-32. C, J, K, O, Q, S (inverted).
Fig. 8 in The evolution of early Spermophilus in eastern Europe and the antiquity of the Old World ground squirrels
Fig. 8. Temporally-calibrated dental variation in P3, P4, M1–M2, M3, p4, and m3 of Spermophilus praecox sp. nov. and Spermophilus nogaici (Topachevsky, 1957). Abbreviations: anl, anteroloph; ants, antesinus; ast, anterostyle; antd, anteroconulid; anv, anterior valley; encd, entoconulid; enl, endoloph; hyd, hypoconid; hyp, hypocone; lanld, labial anterolophid; LH, Late Pleistocene–Holocene; lianld, lingual anterolophid; limtl, lingual metaloph; limtld, lingual metalophid; mes, mesostyle; metl, metaconule; pofd, postflexid; pro, protocone.
Fig. 9 in The evolution of early Spermophilus in eastern Europe and the antiquity of the Old World ground squirrels
Fig. 9. Stratigraphic record of P3 (A), p4 (B), M1–M2 (C), and m1–m2 (D) sizes of Spermophilus praecox sp. nov. (circles) and Spermophilus nogaici Topachevsky, 1957) (triangles). Abbreviations: L, length; W, width; tal.W, talonid width; tri.W, trigonid width.
Fig. 4 in The evolution of early Spermophilus in eastern Europe and the antiquity of the Old World ground squirrels
Fig. 4. Ground squirrel Spermophilus nogaici (Topachevsky, 1957) from the Early and Middle Pleistocene of southern Ukraine and southwestern Russia: Zhevakhova Gora 1 (A, C, N), Tarkhankut (D–F, O, T), Nogaisk (G–J, P, U–W, Z), Moiseevo 1 (Q), Cherevichnoe 1 (B, X), Tihonovka 1 (K, L), Bolshevik 2,I (M), lower cheek teeth (A, B, dp4; C–M, p4; N–S, m1–m2; T–Y, m3; Z, p4–m3), in occlusal (A–Z1), labial (Z2), and lingual (Z3) views. A. NMNHU-P ZG1-20. B. NMNHU-P Che1-41. C. NMNHU-P ZG1-24. D. NMNHU-P 50-26/65. E. NMNHU-P 50-26/110. F. NMNHU-P 50-26/122. G. NMNHU-P 27-106. H. NMNHU-P 27-540. I. NMNHU-P 27-541. J. NMNHU-P 27-543. K. NMNHU-P 29-4066. L. NMNHU-P 29-4075. M. NMNHU-P Bol2/1- 64. N. NMNHU-P ZG1-25. O. NMNHU-P 50-25/131. P. NMNHU-P 27-575. Q. ZIN 105151/33. R. NMNHU-P 29-4079. S. NMNHU-P Bol2/1-73. T. NMNHU-P 50-26/56. U. NMNHU-P 27-161. V. NMNHU-P 27-163. W. NMNHU-P 27-172. X. NMNHU-P Che1-68. Y. NMNHU-P 29-4099. Z. NMNHU-P 27-224. B, D, H, L, T, U, Y (inverted).
Fig. 2 in The evolution of early Spermophilus in eastern Europe and the antiquity of the Old World ground squirrels
Fig. 2. Upper (A) and lower (B) sciurid cheek teeth illustrating the terminology employed here (after Marivaux et al. 2004; Comte et al. 2012; VianeyLiaud et al. 2013; and Maridet et al. 2017; with modifications). Abbreviations: aam, anterior arm of metacone (premetacrista sensu Comte et al. 2012; Vianey-Liaud et al. 2013); aap; anterior arm of protocone; aapa, anterior arm of paracone; alas, anterolabial sinus; anl, anteroloph; ansd, anterosinusid; ant, anterocone; ants, antesinus; ast, anterostyle; antd, anteroconulid; anv, anterior valley; cev, central valley; ecl, ectoloph; ecld, ectolophid; encd, entoconulid; end, entoconid; endr, entoconid ridge; enl, endoloph; enld, entolophid; esd, ectostylid; hyd, hypoconid; hyld, hypoconulid; hyld II, hypoconulid II (second hypoconulid); hyp, hypocone (hypostyle sensu Popova 2016); hyst, hypostyle (hypostyle 2 sensu Popova 2016); lamtl, labial metaloph; lamtld, labial metalophid; lanld, labial anterolophid; laprl, labial protoloph; lianld, lingual anterolophid; liansd, lingual anterosinusid; limtl, lingual metaloph; limtld, lingual metalophid; liprl, lingual protoloph; mecd, mesoconid; med, metaconid; mes, mesostyle; mesd, mesostylid; mesl, metastyle; met, metacone; metd, metastylid; metdtc, metastylid crest; metl, metaconule; metl II, metaconule II (second metaconule); mtld, metalophid; pap, posterior arm of paracone (postparacrista sensu Comte et al. 2012; Vianey-Liaud et al. 2013); par, paracone; parl, paraconule; pasl, parastyle; pasl II, parastyle II (second parastyle); plas, posterolabial sinus; poc, posterocone; pofd, postflexid; pol, posteroloph; pold, posterolophid; pov, posterior valley; prd, protoconid; pro, protocone; prst, protostyle; sd, sinusid; sin, sinus; talb, talonid basin; trdb, trigonid basin.
Fig. 5 in The evolution of early Spermophilus in eastern Europe and the antiquity of the Old World ground squirrels
Fig. 5. Ground squirrel Spermophilus praecox sp. nov. from the Early Pleistocene of southern Ukraine: Kotlovina 3 (A) and Morskoy (B, C); mandibles in lateral (A1–C1), and medial (A2–C2) views. A. ZIN 105163/1. B. ZIN NMNHU-P MoT-63 (inverted). C. NMNHU-P MoT-64.
Fig. 3 in The evolution of early Spermophilus in eastern Europe and the antiquity of the Old World ground squirrels
Fig. 3. Ground squirrel Spermophilus nogaici (Topachevsky, 1957) from the Early and Middle Pleistocene of southern Ukraine and southwestern Russia: Tarkhankut (A, B, G, H, I, O, U), Zhevakhova Gora 1 (F, N, T), Nogaisk (C, J, K, P, V, W, X), Moiseevo 1 (Q), Tihonovka 1 (D, L, R, S, Y, Z), Bolshevik 2,I (M); upper cheek teeth (A–E, P3; F, G, DP4; H–M, P4; N–S, M1–M2; T–Y, M3; Z, P3–M3), in occlusal (A–Z1), labial (Z2), and lingual (Z3) views. A. NMNHU-P 50-29/10. B. NMNHU-P 50-29/11. C. NMNHU-P 27-230. D. NMNHU-P 29-212. E. NMNHU-P Bol2/1-4. F. NMNHU-P ZG1-1. G. NMNHU-P 50-29/69. H. NMNHU-P 50-29/25. I. NMNHU-P 50-29/27. J. NMNHU-P 27-123. K. NMNHU-P 27-239. L. NMNHU-P 29- 216. M. NMNHU-P Bol2/1-24. N. NMNHU-P ZG1-13. O. NMNHU-P 50-27/5. P. NMNHU-P 27-110. Q. ZIN 105151/12. R. NMNHU-P 29-4037. S. NMNHU-P 29-4043. T. NMNHU-P ZG1-17. U. NMNHU-P 50-28/42. V. NMNHU-P 27-535. W. NMNHU-P 27-532. X. NMNHU-P 27-121. Y. NMNHU-P 29-4059. Z. NMNHU-P 29-4036. A–C, D, H–J, P, Q, T, X (inverted).
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