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FIGURE 8 in Diversity of culicomorphan dipterans in the Eocene Kishenehn Konservat-Lagerstätte (Montana, USA) and its palaeoecological implications
FIGURE 8. Hintelmanniella noncatafractata sp. nov. (Chironomidae). Adult males. Paratype USNM 717431 (A–C), specimen USNM 624424 (D). A, Habitus. B, Schematic drawing of male genitalia (hypopygium). C, Male genitalia (hypopygium). D, Hindtibial combs. Abbreviations: gc, gonocoxite; gs, gonostylus; iv, inferior volsella (lateral protrusion of gonocoxite).
FIGURE 2 in Diversity of culicomorphan dipterans in the Eocene Kishenehn Konservat-Lagerstätte (Montana, USA) and its palaeoecological implications
FIGURE 2. Representatives of Chironomidae cf. Conchapelopia. Male pupa USNM 626009. A, Habitus. B, Thoracic horns. C, Male genitalia (hypopygium).
FIGURE 13 in Diversity of culicomorphan dipterans in the Eocene Kishenehn Konservat-Lagerstätte (Montana, USA) and its palaeoecological implications
FIGURE 13. Representatives of Ceratopogonidae cf. Alluaudomyia. Pupa. USNM 623317. A, Habitus, unmarked. B, Habitus, marked. Abbreviations: a2–a8, abdominal units (segments) two to eight; tc, thorax; th, thoracic horn (respiratory organ); wg, wing.
FIGURE 1 in Diversity of culicomorphan dipterans in the Eocene Kishenehn Konservat-Lagerstätte (Montana, USA) and its palaeoecological implications
FIGURE 1. Representatives of Chironomidae cf. Conchapelopia. Male pupa. USNM 621057. A, Habitus, unmarked. B, Habitus, marked. C, Head and thorax, unmarked. D, Head and thorax, marked. Abbreviations: a3–a7, abdominal units (segments) three through seven; ey, compound eyes; gs, genitals; p1, forelegs; p2, midlegs; p3, hindlegs; pd, pedicellus; tc, thorax; th, thoracic horn (respiratory organ); wg, wing.
FIGURE 16 in Diversity of culicomorphan dipterans in the Eocene Kishenehn Konservat-Lagerstätte (Montana, USA) and its palaeoecological implications
FIGURE 16. Chaoborus kishenehnicus sp. nov. (Chaoboridae). Pupa. USNM 623080(A, D), USNM 624863 (B, E), USNM 623356 (C, F). A–C, Habitus, unmarked. D– E, Genitals. F, Thoracic horn (respiratory organs).
FIGURE 12 in Diversity of culicomorphan dipterans in the Eocene Kishenehn Konservat-Lagerstätte (Montana, USA) and its palaeoecological implications
FIGURE 12. Rheotanytarsus lacustris sp. nov. (Chironomidae). Adult male and pupa. Holotype USNM 717577 (A–E). A, Habitus, unmarked. B, Schematic drawing of male genitalia (hypopygium). C, Male genitalia (hypopygium), unmarked. D, Male genitalia (hypopygium), marked. E, Abdominal tergite II with armament of shagreen. Abbreviations: a8–a9, abdominal units (segments) eight and nine; ap, anal point (remnants of tergite X); gc, gonocoxite (II); gs, gonostylus; iv, inferior volsella (lateral protrusion of gonocoxite); mv, median volsella (lateral protrusion of gonocoxite); tb, tergal bands; ts, shagreen of tergites.
FIGURE 17 in Diversity of culicomorphan dipterans in the Eocene Kishenehn Konservat-Lagerstätte (Montana, USA) and its palaeoecological implications
FIGURE 17. Chaoborus kishenehnicus sp. nov. (Chaoboridae). Pupa. USNM 595142. A, Thorax, unmarked. B, Thorax, marked. C, Male genitalia (hypopygium) unmarked. D, Male genitalia (hypopygium), marked. Abbreviations: an, antenna; ey, compound eyes; fc, forecoxa; gc, gonocoxite; gs, genitals; mc, midcoxa; mr, medial rib of the anal paddle; p1, forelegs; p2, midlegs; p3, hindlegs; pd, pedicellus; sc, scutum; su, scutellum; th, thoracic horn (respiratory organ); wg, wing.
FIGURE 20 in Diversity of culicomorphan dipterans in the Eocene Kishenehn Konservat-Lagerstätte (Montana, USA) and its palaeoecological implications
FIGURE 20. Chaoborus kishenehnicus sp. nov. (Chaoboridae). Probably associated females. USNM 624863 (A, B), USNM 623071 (C), USNM 717284 (D). A, C, D, Habitus. B, Spermathecae.
FIGURE 21 in Diversity of culicomorphan dipterans in the Eocene Kishenehn Konservat-Lagerstätte (Montana, USA) and its palaeoecological implications
FIGURE 21. Chaoborus kishenehnicus sp. nov. (Chaoboridae). A, Adult male eclosing from the pupa (USNM622875). B, Male and probably associated female side-by-side, with additional female present (USNM623038).
FIGURE 11 in Diversity of culicomorphan dipterans in the Eocene Kishenehn Konservat-Lagerstätte (Montana, USA) and its palaeoecological implications
FIGURE 11. Rheotanytarsus lacustris sp. nov. (Chironomidae). Pupa. Paratypes USNM 722460 (A–B) and USNM 623669 (C–E). A, Habitus, unmarked. B, Habitus, marked. C, Habitus, unmarked. D, Abdominal tergite III with armament of shagreen. E, Anal lobes and posterolateral comb of abdominal unit 8. Abbreviations: a2–a7, abdominal units (segments) two to seven; al, terminal lobes; tc, thorax; th, thoracic horn (respiratory organ); wg, wing.
FIGURE 14 in Diversity of culicomorphan dipterans in the Eocene Kishenehn Konservat-Lagerstätte (Montana, USA) and its palaeoecological implications
FIGURE 14. Representatives of Ceratopogonidae cf. Alluaudomyia. Pupa. USNM 623317 (A–B), USNM 623326 (C), USNM 624879 (D–F). A, Thorax, unmarked. B, Thorax, marked. C, Thoracic horns. D, Thoracic horns. E, End of abdomen. F, Male genitalia (hypopygium). Abbreviations: an, antenna; ey, compound eyes; p1, forelegs; p2, midlegs; p3, hindlegs; th, thoracic horn (respiratory organ).
FIGURE 6 in Diversity of culicomorphan dipterans in the Eocene Kishenehn Konservat-Lagerstätte (Montana, USA) and its palaeoecological implications
FIGURE 6. Hintelmanniella noncatafractata sp. nov. (Chironomidae). Pupa. Paratype USNM 717431 (A–B) and paratype USNM 717494(C). A, Habitus of the pupa. B, Schematic drawing of the pupa, marked. C, Habitus of the pupa. Abbreviations: a1–a8, abdominal units (segments) one through eight; ct, cephalic tubercles; al, anal lobes; c8, posterolateral comb of abdominal unit 8; fa, frontal apotome; tc, thorax.
FIGURE 22 in Diversity of culicomorphan dipterans in the Eocene Kishenehn Konservat-Lagerstätte (Montana, USA) and its palaeoecological implications
FIGURE 22. Chaoborus kishenehnicus sp. nov. Probably associated egg masses and individual eggs. A, USNM 623795, egg mass. B, USNM 624281, egg. C, USNM 624174, eggs. D, USNM 624230, eggs.
FIGURE 10 in Diversity of culicomorphan dipterans in the Eocene Kishenehn Konservat-Lagerstätte (Montana, USA) and its palaeoecological implications
FIGURE 10. Representatives of Chironomidae cf. Tanytarsus, specimen USNM 722523. Adult male. A, Habitus of the adult male and remnants of a water boatmen nymph (Corixidae). B, Hindtibial combs. C, Male genitalia (hypopygium), unmarked. D, Male genitalia (hypopygium), marked. E, Male genitalia (hypopygium), schematic drawing. Abbreviations: a8–a9, abdominal units (segments) eight and nine; an, antenna; ap, anal point (abdominal unit X remnants); gs, gonostylus; sv, superior volsella (lateral protrusion of gonocoxite).
FIGURE 5 in Diversity of culicomorphan dipterans in the Eocene Kishenehn Konservat-Lagerstätte (Montana, USA) and its palaeoecological implications
FIGURE 5. Representatives of Chironomidae cf. Psectrotanypus. Male pupa USNM 624474.2. A, Habitus, unmarked. B, Habitus, marked. Abbreviations: a2–a7, abdominal units (segments) two through seven; an, antenna; ey, compound eyes; gc, gonocoxite (II); gs, genitals; p1, forelegs; p2, midlegs; p3, hindlegs.
FIGURE 11. A–B in Geographic and temporal variability in Pleistocene lion-like felids: Implications for their evolution and taxonomy
FIGURE 11. A–B: Pearson correlations between the 14 variables and the two PCO axes based on P. leo, P. spelaea, and P. fossilis (thus excluding P. atrox, corresponding to Figure 10B).
FIGURE 10. A in Geographic and temporal variability in Pleistocene lion-like felids: Implications for their evolution and taxonomy
FIGURE 10. A: Principal coordinate analyses based on 14 log-transformed morphometric variables. The first axis is parallel with an overall increase in cranial length. Across its whole range, P. spelaea differs from P. fossilis, and P. fossilis is clearly distinct from P. leo. However, P. spelaea from the Western Europe alone does not differ from P. fossilis. B: Principal coordinate analyses based on 14 log-transformed morphometric variables, excluding P. atrox. This analysis shows that P. spelaea from the Western Europe and the Eastern Europe–Asia do not fully overlap in morphospace. The first PCO axis in both analyses correlates strongly positively with all variables and thus reflects the size axis. Specimen numbers: P. atrox (North America): 1–Ichetucknee, 2–Natural Trap Cave, 3–9–Rancho la Brea; P. fossilis: 10–Mauer (Germany), 11–Azé I-3 (France); P. intermedia: 12–Romain-la-Roche (France), 13–Vence (France), 14–Edingen (Germany), 15–Niedźwiedzia Cave (Poland), 16–San (Poland); P. spelaea: 17–Bottrop (Germany), 18– Huttenheim (Germany), 19–Perickhöhlen (Germany), 20–Siegsdorf (Germany), 21–Zoolithenhöhle (holotype; Germany), 22–24–Zoolithenhöhle (Germany), 25–Zandobbio (Italy), 26–Brno (Czech R.), 27–Sloup (Vienna specimen; Czech R.), 28–Sloup (OK 130570, Czech R.), 29–Srbsko–Chlum Komín Cave (Czech R.), 30–Výpustek 1 (Czech R.), 31–Výpustek 3 (Czech R.), 32–Igrita (Croatia), 33–Ursilor (Romania), 34–Binagady (Caucasus, Georgia), 35–Desna (Russia), 36–37–Isa River (South Ural, Russia), 38–Kondakovka (Russia), 39–Mokhokho (Russia), 40–Uzhur (Central Siberia), 41–42–Medvedia Cave (Slovakia); P. leo (Africa and India): 43–50.
FIGURE 8 in Geographic and temporal variability in Pleistocene lion-like felids: Implications for their evolution and taxonomy
FIGURE 8. Bivariate relationships between the cranial length and nine morphological variables. The lines represent slopes of the relationship between the log-transformed cranial length and nine variables fitted by reduced major axis regression separately for P. fossilis, P. spelaea, and P. leo. Axes are logged.
FIGURE 9 in Geographic and temporal variability in Pleistocene lion-like felids: Implications for their evolution and taxonomy
FIGURE 9. The summary of mean allometric coefficients (slopes of the relationship between the log-transformed cranial length and nine variables fitted by reduced major axis regression) with 95% bootstrapped confidence intervals. They show more positive allometry for mastoid width, canine width, medial nasale length, and lateral nasal length in P. fossilis relative to other three species (although 95% confidence intervals are broad). The postorbital width shows negative allometry in P. leo whereas it shows positive allometry in P. spelaea and P. fossilis. The missing values in P. atrox did not allow to measure its allometric coefficients for lateral nasal length.
FIGURE 6 in Geographic and temporal variability in Pleistocene lion-like felids: Implications for their evolution and taxonomy
FIGURE 6. Different types of lion heads in Paleolithic art, maybe indicating the cranial profile type 2 (A), probably the cranial profile type 1 (B), and the cranial profile type 0 (C-F). A: a lion head sculpture from Kostenki near Voronezh, Russia (ca. 23 ka BP, redrawn from Efimenko 1958); B: a lion head sculpture from Vogelherd, Germany (ca. 38-33 ka BP, redrawn from Koenigswald and Schmitt 1987); C: a lion head sculpture from Dolní Věstonice, Moravia–Czech Republic (ca. 27-29 ka BP, redrawn from Jelínek 1972); D: a cave lion depicted in La Marche, France (Magdalenian); E: cave lion pair depicted in Chauvet, France (˂ 26 ka BP); F: cave lions depicted in Chauvet, France (˂ 26 ka BP, redrawn from Clottes 2001). © J. Gullár, 2009-2014 (A–C, F) and the archive of M. Sabol (D and E). Author of illustrations A–C and F is J. Gullár (please, cite it as: J. Gullár in Sabol et al., 2022); D and E are from the archive of M. Sabol.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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OpenNeuro
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