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opennotspecifiedFeb 2013View details →

Fig. 4 in Quaternary refugia in southwestern Iran: insights from two sympatric moth species (Insecta, Lepidoptera)

Fig. 4 Mismatch distribution and tests of selective neutrality. Dotted line: The observed distribution; solid line: the expected distribution after past population expansion. For the neutrality tests, P-values are provided in brackets. Significant results are marked in bold. Hri: Harpending's raggedness index; SDD: sum of squared deviations

opennotspecifiedNov 2002View details →

Figure 1 in Herpetofauna Of The Quaternary Sand Dunes Of The Middle Rio São Francisco: Bahia: Brazil. Vii. Typhlops Amoipira Sp. Nov., A Possible Relative Of Typhlops Yonenagae (Serpentes, Typhlopidae)

Figure 1. Typhlops amoipira, sp. nov.: lateral, ventral, and dorsal views of head (MZUSP 12298, holotype)

FIGURE 61 in Late Quaternary Chrysophycean stomatocysts in a Southern Carpathian mountain lake, including the description of new forms (Romania)

FIGURE 61. The relative abundances of some siliceous fossils in Lake Gales, and the ratio of cysts and diatoms.

FIGURES 41–60 in Late Quaternary Chrysophycean stomatocysts in a Southern Carpathian mountain lake, including the description of new forms (Romania)

FIGURES 41–60 The most characteristic stomatocysts of Lake Gales according to their occurrences in the upper five diatom assemblages' zones (between DAZ–6 and DAZ–10). Figs 41–44 DAZ–6: Fig. 41. C072—180 cm; Fig. 42. C050 —180 cm; Fig. 43. C072—180 cm; Fig. 44. C166—180 cm; Figs 45–48 DAZ–7: Fig. 45. C001—168 cm; Fig. 46. C198—168 cm; Fig. 47. C148—168 cm; Fig. 48. C337– 176 cm; Figs 49–52 DAZ–8 Fig. 49. C057– 104 cm; Fig. 50. C324—168 cm; Fig. 51. C004—88 cm; Fig. 52. C180—104 cm; Figs 53–56 DAZ–9: Fig. 53. C133—48 cm; Fig. 54. C220—56 cm; Fig. 55. C092—168 cm; Fig. 56. C357—48 cm; Figs 57–60 DAZ–10: Fig. 57. C336—2 cm; Fig. 58. C035—2 cm; Fig. 59. C243—2 cm; Fig. 60. C345—2 cm.

FIGURES 21–40 in Late Quaternary Chrysophycean stomatocysts in a Southern Carpathian mountain lake, including the description of new forms (Romania)

FIGURES 21–40 The most characteristic stomatocysts of Lake Gales according to their occurrences in the first five diatom assemblages' zones (between DAZ–1 and DAZ–5). Figs 21–24 DAZ–1: Fig. 21. C116—264 cm, Fig. 22. C049—264 cm; Fig. 23. C189—264 cm; Fig. 24; C300B—264 cm; Figs 25–29 DAZ–2: Fig 25. C210—260 cm; Fig. 26. C169—260 cm, Fig. 27. C135—260 cm; Fig. 28. "Unidentified stomatocyst 14"—260 cm; Fig. 29. C079—260 cm; Figs 30–33, DAZ–3: Fig. 30. C189—236 cm, Fig. 31. C318—236 cm; Figs 32–33 C360—236 cm; Figs 34–37 DAZ–4: Fig. 34. C120—196 cm; Fig. 35. C202—196 cm; Fig. 36. C239—196 cm; Fig. 37. C148 note the short, thin spines that are roughly equidistant—196 cm; Figs 38–40 DAZ–5: Fig. 38. C121—188 cm, Fig. 39. C169—188 cm; Fig. 40. C009—188 cm.

FIGURE 20 in Late Quaternary Chrysophycean stomatocysts in a Southern Carpathian mountain lake, including the description of new forms (Romania)

FIGURE 20. Relative abundances and zonation of the most common diatoms in Lake Gales. Diatoms were ordered according to their occurrences.

FIGURES 1–19 in Late Quaternary Chrysophycean stomatocysts in a Southern Carpathian mountain lake, including the description of new forms (Romania)

FIGURES 1–19 Scanning electron and light microscope pictures of new morphotypes were found in Lake Gales sediment core (Gales–3) Figs 1–7 Scanning electron microscope Figs 8–19. Light microscope Figs 1, 8–9 C500; Figs 2, 10–11 C501; Figs 3, 12–13 C502; Figs 4, 14–15 C503; Figs 5, 16 C504; Figs 6, 17–18 C505; Figs 7, 19 C506. Scale bar is 10 µm in LM pictures.

Figure 7 in Reflection of the Neogene-Quaternary phylogeography in the recent distribution limiting climatic factors of eight Mediterranean Phlebotomus species (Diptera: Psychodidae)

Figure 7. The hierarchical factor analysis of the monthly mean temperature values (°C), the maximum of the monthly mean temperature values (°C), the minimum of the monthly minimum temperature values (°C), the maximum of the monthly minimum temperature values (°C), the minimum of the monthly precipitation values (mm) and the maximum of the monthly precipitation values (mm) limits of the eight studied Phlebotomus species.

Figure 2 in Reflection of the Neogene-Quaternary phylogeography in the recent distribution limiting climatic factors of eight Mediterranean Phlebotomus species (Diptera: Psychodidae)

Figure 2. Jaccard indices of countrywide sand fly diversities according to the Italy focus, based on the eight involved Phlebotomus species.

Figure 6 in Reflection of the Neogene-Quaternary phylogeography in the recent distribution limiting climatic factors of eight Mediterranean Phlebotomus species (Diptera: Psychodidae)

Figure 6. The principal component analysis result of the eight studied Phlebotomus species according to the maximum monthly precipitation value limits of the species.

Figure 10 in Reflection of the Neogene-Quaternary phylogeography in the recent distribution limiting climatic factors of eight Mediterranean Phlebotomus species (Diptera: Psychodidae)

Figure 10. The aggregated distribution of the species of the 'West-Mediterranean group' (absence: empty, presence: red fields; NUTS 3 regions).

Figure 9 in Reflection of the Neogene-Quaternary phylogeography in the recent distribution limiting climatic factors of eight Mediterranean Phlebotomus species (Diptera: Psychodidae)

Figure 9. The aggregated distribution of the species of the 'East-Mediterranean group' (absence: empty, presence: red fields; NUTS 3 regions).

Figure 1 in Reflection of the Neogene-Quaternary phylogeography in the recent distribution limiting climatic factors of eight Mediterranean Phlebotomus species (Diptera: Psychodidae)

Figure 1. Jaccard indices of countrywide sand fly diversities according to the Portugal focus, based on the eight involved Phlebotomus species.

Figure 8 in Reflection of the Neogene-Quaternary phylogeography in the recent distribution limiting climatic factors of eight Mediterranean Phlebotomus species (Diptera: Psychodidae)

Figure 8. The aggregated distribution of the species of the 'Trans-Mediterranean group' (absence: empty, presence: red fields; NUTS 3 regions).

Figure 4 in Reflection of the Neogene-Quaternary phylogeography in the recent distribution limiting climatic factors of eight Mediterranean Phlebotomus species (Diptera: Psychodidae)

Figure 4. The hierarchical cluster analysis result of the eight studied Phlebotomus species according to their presence/absence status in the studied countries (CH, Switzerland; D, Germany; I, Italy; P, Portugal; E, Spain; F, France; TR, Turkey; CY, Cyprus; BG, Bulgaria; BIH, Bosnia and Herzegovina; AL, Albania; MNE, Montenegro; GR, Greece; RO, Romania; KOS, Kosovo; HR, Croatia; SRB, Serbia; MD, Moldova; H, Hungary; MK, Macedonia.

Figure 3 in Reflection of the Neogene-Quaternary phylogeography in the recent distribution limiting climatic factors of eight Mediterranean Phlebotomus species (Diptera: Psychodidae)

Figure 3. Jaccard indices of countrywide sand fly diversities according to the Greece focus, based on the eight involved Phlebotomus species.

Figure 11 in Reflection of the Neogene-Quaternary phylogeography in the recent distribution limiting climatic factors of eight Mediterranean Phlebotomus species (Diptera: Psychodidae)

Figure 11. The geographical and climatic reconstruction maps for the European Early Late and Middle Miocene era with the mean annual temperature values according to the Neogene Climate Evolution in Eurasia model, based on the findings of Bruch et al. (2007). The yellow dashed line shows the climate border in the region of the Paratethys Sea.

opennotspecifiedOct 2010View details →

FIGURE 3. A–F Conilurus albipes. A. QMF54064 right maxilla with heavily worn M1-3 in New Quaternary records of Conilurus (Rodentia: Muridae) from eastern and northern Australia with the description of a new species

FIGURE 3. A–F Conilurus albipes. A. QMF54064 right maxilla with heavily worn M1-3; B. QMF54065 right maxilla with M1-3; C. QMF52052 left maxilla with M1-2; D–E QMF54066 left mandible with I and M; F. QMF54073 left M1; 1 1-3 G–H C. penicillatus. G. QMF54058 right M1; H. left M1; I–J tree rat, indet. sp. I. QMF54078 right M1; J. QMF54075 right maxilla with M1-2. Scale bars= 2mm.

opennotspecifiedOct 2010View details →

FIGURE 1 in New Quaternary records of Conilurus (Rodentia: Muridae) from eastern and northern Australia with the description of a new species

FIGURE 1. Map of fossil sites mentioned in the text, with distributions of Conilurus species (from Menkhorst and Knight 2001). Pale grey represents historically known distributions, dark grey represents known extant distributions. Conilurus penicillatus is also found in southern New Guinea (not shown).