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Seismic noise recorded at Solfatara Volcano in April 2007
<p>Seismic noise recorded during a seismic survey carried out at Solfatara Volcano in the period 2-6 April 2007. Five circular seismic arrays were deployed inside the crater; an other seismic station was installed on the eastern rim for a hardrock reference. Details on the experiment, as well as data description and station coordinates are reported in: Petrosino, S., Damiano, N., Cusano, P., Veneruso, M., Zaccarelli, L., Torello, V., & Del Pezzo, E. (2008). Seismic noise at Solfatara Volcano (Campi Flegrei, Italy): acquisition techniques and first results. <em>Quaderni di Geofisica</em>.</p> <p>Shallow crustal structure of Solfatara volcano, inferred from dataset analysis has been published in: Petrosino, S., Damiano, N., Cusano, P., Di Vito, M. A., de Vita, S., & Del Pezzo, E. (2012). Subsurface structure of the Solfatara volcano (Campi Flegrei caldera, Italy) as deduced from joint seismic‐noise array, volcanological and morphostructural analysis. <em>Geochemistry, Geophysics, Geosystems</em>, <em>13</em>(7).</p>
Figures 1-6 in Bolivian Rhinotragini XI. New species of Phygopoda Thomson, 1864 and Phygopoides Peñaherrera-Leiva and Tavakilian, 2007 (Coleoptera, Cerambycidae)
Figures 1-6. New species of Phygopoda Thomson, 1864. Fig. 1-3. P. longiscopifera sp. nov. 1) Male holotype. 2) Female allotype, black form. 3) Female paratype, rufous form. Fig. 4. P. boliviensis sp. nov., male holotype. Fig. 5- 6. P. chaquensis sp. nov. 5) Male holotype. 6) Female allotype.
Figure 8 in Review of Carelli, A., and M.L. Monné, 2015. Taxonomic revision of Phygopoda Thomson, 1864 and Pseudophygopoda Tavakilian & Peñaherrera-Leiva, 2007 (Insecta: Coleoptera: Cerambycidae: Cerambycinae)
Figure 8. Tegmen of aedeagus in Pseudophygopoda (after Carelli and Monné (2015)), l-r dorsal, lateral, and ventral views. 8a) P. subvestita. 8b) P. albitarsis.
Figures 4-7 in Review of Carelli, A., and M.L. Monné, 2015. Taxonomic revision of Phygopoda Thomson, 1864 and Pseudophygopoda Tavakilian & Peñaherrera-Leiva, 2007 (Insecta: Coleoptera: Cerambycidae: Cerambycinae)
Figures 4-7. Male genitalia: Tegmen of aedeagus (after Clarke (2014)). 4) Pseudophygopoda subvestita. 5) Paraphygopoda albitarsis. 6) Paraphygopoda viridimicans. 7) Phygomelitta triangularis.
Figure 2 in Review of Carelli, A., and M.L. Monné, 2015. Taxonomic revision of Phygopoda Thomson, 1864 and Pseudophygopoda Tavakilian & Peñaherrera-Leiva, 2007 (Insecta: Coleoptera: Cerambycidae: Cerambycinae)
Figure 2. Left: Tegmen of Neophygopoda tibialis. Right: Illustration of tegmen of Phygopoda nigritarsis, from Carelli and Monné (2015).
Figures 7-10 in Bolivian Rhinotragini XI. New species of Phygopoda Thomson, 1864 and Phygopoides Peñaherrera-Leiva and Tavakilian, 2007 (Coleoptera, Cerambycidae)
Figures 7-10. Phygopoides maxwelli sp. nov. 7) Male holotype. 8) Male paratype, rufous form. 9) Female allotype, rufous form. 10) Genitalia male holotype, in situ, showing structure of tegmen.
Fig. 1 in Abstracts of the Immature Beetles Meeting 2007
Fig. 1: Participants of the Immature Beetles Meeting 2007 on October 4, 2007. From left to right: back row: D. Král, J. Prokop, J. Hájek, J. Skuhrovec, A. Kilian, P. Saska, M. Perreau, J. Kolibáč, D. Ahrens, J. A. Delgado, M. A. Ivie, A. Di Giulio, P. Hlaváč, and P. Švácha; front row: J. Boháč, V. V. Grebennikov, M. Fikáček, and C. Maier.
Figs 3-5 in Abstracts of the Immature Beetles Meeting 2007
Figs 3-5 (to the abstract by Bílý & Prokop, p. 292). 3: adult larva of Coraebus undulatus (F.); 4: sclerotization of the last abdominal segment of larva of Coraebus florentinus (Herbst, 1801); 5: fossil of the last abdominal segment of a larva of Agrilinae gen. et sp. indet. (spec. No. JD2080: Jaroslav Dolejš private collection, Prague), Late Eocene, Kučlín near Bílina (Czech Republic).
Fig. 5. A, B, a in A new species of the genus Indochinamon Yeo & Ng, 2007 (Crustacea: Brachyura: Potamoidea: Potamidae) from northern Vietnam
Fig. 5. A, B, a habitat in Huong Pagoda, Huong Son commune, My Duc district, Ha Noi province, Vietnam; C, D, Indochinamon chuahuong, new species, in a cage being offered for sale to tourists.
Fig. 4 in A new species of the genus Indochinamon Yeo & Ng, 2007 (Crustacea: Brachyura: Potamoidea: Potamidae) from northern Vietnam
Fig. 4. Indochinamon chuahuong, new species, holotype male (76.1 × 53.0 mm) (IBER-FC IC×01), Huong Pagoda, Huong Son commune, My Duc district, Ha Noi province, Vietnam. A, ventral view of left G1; B, ventral view of distal part of left G1; C, dorsal view of left G1; D, dorsal view of distal part of left G1; E, lateral view of left G1; F, lateral view distal part of left G1; G, dorsal view of left G2; H, left G2 of terminal segment.
Fig. 3 in A new species of the genus Indochinamon Yeo & Ng, 2007 (Crustacea: Brachyura: Potamoidea: Potamidae) from northern Vietnam
Fig. 3. Indochinamon chuahuong, new species, holotype male (76.1 × 53.0 mm) (IBER-FC IC×01), Huong Pagoda, Huong Son commune, My Duc district, Ha Noi province, Vietnam. A, ventral view showing anterior thoracic sternum and abdomen; B, left third maxilliped; C, chela outer view.
Fig. 2 in A new species of the genus Indochinamon Yeo & Ng, 2007 (Crustacea: Brachyura: Potamoidea: Potamidae) from northern Vietnam
Fig. 2. Indochinamon chuahuong, new species, holotype male (76.1 × 53.0 mm) (IBER-FC IC×01), Huong Pagoda, Huong Son commune, My Duc district, Ha Noi province, Vietnam. A, overall habitus; B, dorsal view of carapace; C, frontal view of carapace.
Text-fig. 4. Location Map of the examined water vole localities. From Masini et al. (2007), modified. 1: Madrid, surroundings, 2: Graz, 3: Eisfeld, 4: Langen, 5: Delta Po, 6: Rovigo, 7: Ferrara, 8: Calabria, 9: Caverna degli Orsi, 10: Arma delle Manie, 11: Riparo Mochi, 12: Grotta di Castelcivita, 13: Grotta della Serratura, 14: Grotta del Romito, 15: Scario Grotta Grande, 16: Grotta di Cucigliana, 17: Upper Valdarno Campitello, 18: Riparo di Visogliano, 19: Isernia La Pineta, 20: Baume Gigny, 21: Baume Moula Guercy, 22: Grotte de L'Eglise, 23: Grotte-Abri Suard, 24: Grotte d'Artenac, 25: Pié Lombard, 26: Abri Vaufrey, 27: Grotte du Lazaret, 28: Abri Gaudry, 29: Pisede, 30: Euerwanger Bühl, 31: Kemathenhöhle, 32: Krockstein (Rübeland 1), 33: Burgtonna, 34: Parkhöhle (Weimar), 35: Stuttgart- Untertürkheim, 36: Taubach, 37: Ehringsdorf, 38: Plaidter-Hummerich, 39: Mosbach, 40: Petersbuch 1, 41: Bilzingsleben, 42: Miesenheim 1, 43: Voigtstedt, 44: Untermassfeld. See Table 1 for symbol explanations. in Independent Water Vole (Mimomys Savini, Arvicola: Rodentia, Mammalia) Lineages In Italy And Central Europe
Text-fig. 4. Location Map of the examined water vole localities. From Masini et al. (2007), modified. 1: Madrid, surroundings, 2: Graz, 3: Eisfeld, 4: Langen, 5: Delta Po, 6: Rovigo, 7: Ferrara, 8: Calabria, 9: Caverna degli Orsi, 10: Arma delle Manie, 11: Riparo Mochi, 12: Grotta di Castelcivita, 13: Grotta della Serratura, 14: Grotta del Romito, 15: Scario Grotta Grande, 16: Grotta di Cucigliana, 17: Upper Valdarno Campitello, 18: Riparo di Visogliano, 19: Isernia La Pineta, 20: Baume Gigny, 21: Baume Moula Guercy, 22: Grotte de L'Eglise, 23: Grotte-Abri Suard, 24: Grotte d'Artenac, 25: Pié Lombard, 26: Abri Vaufrey, 27: Grotte du Lazaret, 28: Abri Gaudry, 29: Pisede, 30: Euerwanger Bühl, 31: Kemathenhöhle, 32: Krockstein (Rübeland 1), 33: Burgtonna, 34: Parkhöhle (Weimar), 35: Stuttgart- Untertürkheim, 36: Taubach, 37: Ehringsdorf, 38: Plaidter-Hummerich, 39: Mosbach, 40: Petersbuch 1, 41: Bilzingsleben, 42: Miesenheim 1, 43: Voigtstedt, 44: Untermassfeld. See Table 1 for symbol explanations.
Text-fig. 2. Generalised stratigraphy of the area including the fossil site in Orta-Şabanözü (Sengüler 2007). The coloured formation is Hüyükköy Formation, aged as late Miocene and containing fossil woods. in The First Glyptostroboxylon And Taxodioxylon Descriptions From The Late Miocene Of Turkey And Palaeoclimatological Evaluation
Text-fig. 2. Generalised stratigraphy of the area including the fossil site in Orta-Şabanözü (Sengüler 2007). The coloured formation is Hüyükköy Formation, aged as late Miocene and containing fossil woods.
Text-fig. 1. Sampling areas in Çankırı province: the village of Sakarcaören near to the town of Orta (green circle) in the east of GVP, and the other sites (yellow circles), volcanic centers (red circles) and the border of GVP. The sites marked as yellow circles: ELM, Elmali village; SOG, Soguksu National Park; BUG, Bugralar village; INO, Inozu Valley South Side; INL, Inozu Valley North Side; KAR, Karasar village; MEN, Menceler Plateau; KIR, Kiraluc Site near Nuhhoca village; AGU, Asagiguney village; KUZ, Kuzca village (Bayam et al. 2018); PEL, Pelitcik village (Akkemik et al. 2009); GUD, Gudul (Akkemik et al. 2017); HOC, Hoçaş village and KOZ, Kozyaka village (Akkemik et al. 2016). The sites located in the western part (INO, INL, KAR, MEN, KIR, AGU, KUZ, HOC and KUZ) are from early – middle Burdigalian and Hancili Formation (Altun et al. 2002, Akbaş et al. 2002). The sites in the central part (GUD, BUG, ELM, PEL and SOG) are from middle – late Burdigalian, Pazar Formation (Kazancı 2012, Sen et al. 2017), and finally the fossil site in the east part of GVP is the late Miocene, Hüyükköy Formation (Sengüler 2007). in The First Glyptostroboxylon And Taxodioxylon Descriptions From The Late Miocene Of Turkey And Palaeoclimatological Evaluation
Text-fig. 1. Sampling areas in Çankırı province: the village of Sakarcaören near to the town of Orta (green circle) in the east of GVP, and the other sites (yellow circles), volcanic centers (red circles) and the border of GVP. The sites marked as yellow circles: ELM, Elmali village; SOG, Soguksu National Park; BUG, Bugralar village; INO, Inozu Valley South Side; INL, Inozu Valley North Side; KAR, Karasar village; MEN, Menceler Plateau; KIR, Kiraluc Site near Nuhhoca village; AGU, Asagiguney village; KUZ, Kuzca village (Bayam et al. 2018); PEL, Pelitcik village (Akkemik et al. 2009); GUD, Gudul (Akkemik et al. 2017); HOC, Hoçaş village and KOZ, Kozyaka village (Akkemik et al. 2016). The sites located in the western part (INO, INL, KAR, MEN, KIR, AGU, KUZ, HOC and KUZ) are from early – middle Burdigalian and Hancili Formation (Altun et al. 2002, Akbaş et al. 2002). The sites in the central part (GUD, BUG, ELM, PEL and SOG) are from middle – late Burdigalian, Pazar Formation (Kazancı 2012, Sen et al. 2017), and finally the fossil site in the east part of GVP is the late Miocene, Hüyükköy Formation (Sengüler 2007).
Text-fig. 4. Bivariate plots of the upper teeth (M2 – P3) of small to medium sized Miocene hyaenodonts from African localities. Data source: Pilgrim (1912, 1914, 1932), Colbert (1935), Savage (1965), Barry (1988), Morales et al. (1998a, 2007), Holroyd (1999), Rasmussen et al. (2009), Borths et al. (2016), Borths and Seiffert (2017). in New Hyaenodonts (Ferae, Mammalia) From The Early Miocene Of Napak (Uganda), Koru (Kenya) And Grillental (Namibia)
Text-fig. 4. Bivariate plots of the upper teeth (M2 – P3) of small to medium sized Miocene hyaenodonts from African localities. Data source: Pilgrim (1912, 1914, 1932), Colbert (1935), Savage (1965), Barry (1988), Morales et al. (1998a, 2007), Holroyd (1999), Rasmussen et al. (2009), Borths et al. (2016), Borths and Seiffert (2017).
Text-fig. 3. Bivariate plots of the lower teeth (m3 – m2) of small to medium sized Miocene hyaenodonts from African localities. Data source: Pilgrim (1912, 1932), Colbert (1935), Savage (1965), Barry (1988), Morales et al. (1998a, 2003, 2007, 2008, 2010), Holroyd (1999), Morlo et al. (2007), Rasmussen et al. (2009), Borths et al. (2016), Borths and Seiffert (2017). in New Hyaenodonts (Ferae, Mammalia) From The Early Miocene Of Napak (Uganda), Koru (Kenya) And Grillental (Namibia)
Text-fig. 3. Bivariate plots of the lower teeth (m3 – m2) of small to medium sized Miocene hyaenodonts from African localities. Data source: Pilgrim (1912, 1932), Colbert (1935), Savage (1965), Barry (1988), Morales et al. (1998a, 2003, 2007, 2008, 2010), Holroyd (1999), Morlo et al. (2007), Rasmussen et al. (2009), Borths et al. (2016), Borths and Seiffert (2017).
Text-fig. 7. Bivariate plots of the upper teeth (M2, M1, P4) and lower teeth (m3, m2, p4) of large Miocene hyaenodonts from Eurasian and African localities. Data source: Stromer (1926), Savage (1965), Barry (1988), Ginsburg (1999), Holroyd (1999), Morales et al. (2003, 2007, 2008, 2010), Morlo et al. (2007), Rasmussen and Gutiérrez (2009), Borths et al. (2016). in New Hyaenodonts (Ferae, Mammalia) From The Early Miocene Of Napak (Uganda), Koru (Kenya) And Grillental (Namibia)
Text-fig. 7. Bivariate plots of the upper teeth (M2, M1, P4) and lower teeth (m3, m2, p4) of large Miocene hyaenodonts from Eurasian and African localities. Data source: Stromer (1926), Savage (1965), Barry (1988), Ginsburg (1999), Holroyd (1999), Morales et al. (2003, 2007, 2008, 2010), Morlo et al. (2007), Rasmussen and Gutiérrez (2009), Borths et al. (2016).
Text-fig. 3. Scatter diagram of mean L/W values of selected Spermophilinus upper first molars (M1 and M2) from Switzerland and south Germany. The crosses correspond to the minimum and maximum values of the length and width. The intersection gives the value of the mean. Comparative data are after Ziegler and Fahlbusch (1986), Bolliger (1992), Kälin (1993), Ziegler (1995, 2005), Kälin and Engesser (2001), Prieto (2007), Prieto et al. (2009, 2017), Seehuber (2009). Blue: localities younger than ~14 Ma (S. bredai); Green: localities ranging from ~14 Ma to ~15Ma (S. bredai); Red: localities ranging from ~15 Ma to ~16 Ma (S. besana); Yellow: older localities (most S. besana). in Dental Anomaly In A Middle Miocene Fossil Of The Genus Spermophilinus (Rodentia, Sciuridae) From Southern Germany
Text-fig. 3. Scatter diagram of mean L/W values of selected Spermophilinus upper first molars (M1 and M2) from Switzerland and south Germany. The crosses correspond to the minimum and maximum values of the length and width. The intersection gives the value of the mean. Comparative data are after Ziegler and Fahlbusch (1986), Bolliger (1992), Kälin (1993), Ziegler (1995, 2005), Kälin and Engesser (2001), Prieto (2007), Prieto et al. (2009, 2017), Seehuber (2009). Blue: localities younger than ~14 Ma (S. bredai); Green: localities ranging from ~14 Ma to ~15Ma (S. bredai); Red: localities ranging from ~15 Ma to ~16 Ma (S. besana); Yellow: older localities (most S. besana).
TYPES: Male holotype from Panama: Panama: Parque Nacional Altos de Campana, 1 hectare PANCODING Inventory, 895 m, 8.68333°, -79.92972°, June 14–19, 2007, M. Arnedo, D. Dimitrov, G. Hormiga, F. Labarque, M. Ramírez, deposited in MIUP, PBI_OON 42313; same data, 1 male paratype deposited in MACN-Ar 29895, PBI_OON 42312. ETYMOLOGY: A noun in apposition; in Greek religion and mythology, Pan is the god of the wild natural world, of shepherds, flocks, and mountains, and of hunting and rustic music. He has hindquarters, legs, and horns of a goat, and the name is here employed to note the large mac- rosetae at the eye region of males that resemble the horns in some illustrations of this god. DIAGNOSIS: This is one of the most autapomor- phic species from the Americas; males have the labium fused with the sternum (fig. 34B), small chelicerae, shorter than the endite length, with anterior blunt projections, and directed backward in lateral view (fig. 34D, E); clypeus directed back- ward (fig. 34D); two light areas on the sternum just below the endites (fig. 34B), carapace almost flat in lateral view and two strong macrosetae at the eye region, pointing forward (fig. 34C–E). Other characters of the male palp, such as the presence of two apophyses, also distinguish this species from others (fig. 38D–F). MALE (PBI_OON 42312): Total length 1.00. Habitus as in figure 34A–C. CEPHALOTHO- RAX: Carapace orange, with brown stripe along in Taxonomic Revision Of The Jumping Goblin Spiders Of The Genus Orchestina Simon, 1882, In The Americas (Araneae: Oonopidae)
TYPES: Male holotype from Panama: Panama: Parque Nacional Altos de Campana, 1 hectare PANCODING Inventory, 895 m, 8.68333°, -79.92972°, June 14–19, 2007, M. Arnedo, D. Dimitrov, G. Hormiga, F. Labarque, M. Ramírez, deposited in MIUP, PBI_OON 42313; same data, 1 male paratype deposited in MACN-Ar 29895, PBI_OON 42312. ETYMOLOGY: A noun in apposition; in Greek religion and mythology, Pan is the god of the wild natural world, of shepherds, flocks, and mountains, and of hunting and rustic music. He has hindquarters, legs, and horns of a goat, and the name is here employed to note the large mac- rosetae at the eye region of males that resemble the horns in some illustrations of this god. DIAGNOSIS: This is one of the most autapomor- phic species from the Americas; males have the labium fused with the sternum (fig. 34B), small chelicerae, shorter than the endite length, with anterior blunt projections, and directed backward in lateral view (fig. 34D, E); clypeus directed back- ward (fig. 34D); two light areas on the sternum just below the endites (fig. 34B), carapace almost flat in lateral view and two strong macrosetae at the eye region, pointing forward (fig. 34C–E). Other characters of the male palp, such as the presence of two apophyses, also distinguish this species from others (fig. 38D–F). MALE (PBI_OON 42312): Total length 1.00. Habitus as in figure 34A–C. CEPHALOTHO- RAX: Carapace orange, with brown stripe along
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Allen Brain Atlas
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OpenNeuro
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