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FIGURES 13−15 in Six new species of the genus Meleonoma Meyrick, 1914 (Lepidoptera: Autostichidae) from China
FIGURES 13−15. Female genitalia of Meleonoma spp. 13, M. dorsidentata sp. nov., slide No. ZXJ19517; 14, M. hirsuta sp. nov., slide No. ZXJ19622; 15, M. longibursoides sp. nov., slide No. ZXJ19624. All paratypes. Scale bars = 0.5 mm.
FIGURES 7−12 in Six new species of the genus Meleonoma Meyrick, 1914 (Lepidoptera: Autostichidae) from China
FIGURES 7−12. Male genitalia of Meleonoma spp. 7, M. avicapitata sp. nov., paratype, slide No. ZXJ19199; 8, M. bitaeniana sp. nov., holotype, slide No. ZXJ19154; 9, M. dorsidentata sp. nov., holotype, slide No. ZXJ19516; 10, M. hirsuta sp. nov., holotype, slide No. ZXJ19499; 11, M. longibursoides sp. nov., holotype, slide No. ZXJ19350; 12, M. spiculata sp. nov., holotype, slide No. ZXJ19357. Scale bars = 0.5 mm.
Figure 10 in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 10. Nest location of Quindina sanantonio sp. n. (A–E) and Quindina horologium sp. n. (F) in leaves. (A) Nest #1; (B) nest #2; (C) nest #3; (D) nest #4; (E) nest #5. Scale bars = 10 mm.
Figure 9 in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 9. Nest of Quindina sanantonio sp. n. (A) Close-up of nest #1. (B) Egg with immature harvestmen.
Figure 1 in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 1. Quindina sanantonio sp. n. (A–F) Male holotype (MUSENUV-Ar-2240): Habitus in dorsal (A), ventral (B) and lateral (C) views. Female paratype (MUSENUV-Ar-2247): Habitus in dorsal (D), ventral (E) and lateral (F) views. Quindina horologium sp. n: (G–L) Male holotype (MUSENUV-Ar-2229): Habitus in dorsal (G), ventral (H) and lateral (I) views. Female paratype (MUSENUV-Ar-2230): Habitus in dorsal (J), ventral (K) and lateral (L) views. Scale bars = 1 mm.
Figure 5. Topology obtained under K in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 5. Topology obtained under K = 7; only the family Nomoclastidae is displayed. Numbers above branches indicate Bootstrap support with absolute frequency (left) and Group present/Contradicted values (right), square brackets indicate negative differences. Navajo rugs: NE, Nelsen strict consensus under equal weighting; K, implied weighting (K 3, 4, 5, 6, 7, 8, 9, 10, 15). Next to each species are depicted the codes for the character #96 (Nest architecture) and a photograph for each state in the box on the right. Nest type 0 photo by Rosanette Quesada.
Figure 4 in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 4. Quindina sanantonio sp. n. (A–C) Quindina horologium sp. n. (D–F) Penis in dorsal (A, D), ventral (B, E) and lateral (C, F) views. Abbreviations: A = macrosetae A, C = macrosetae C, E = macrosetae E. Scale bars = 50 mm.
Figure 2 in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 2. Quindina sanantonio sp. n. (A–E) Male holotype (MUSENUV-Ar-2240): (A) Habitus, dorsal view; (B) lateral view. (C) Left pedipalp, ventral view, trochanter to tarsus. (D) Leg I, tibia to tarsus in prolateral view. (E) Chelicera (hand, fixed and movable fingers). Scale bars = 1 mm.
Figure 6. Topology obtained under K in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 6. Topology obtained under K = 7, with unambiguous character optimisations shown in each branch. Empty and filled hashmarks represent homoplasious and non-homoplasious transformations, respectively, with characters on top and states below. Only the genera Callcosma and Quindina are displayed.
Figure 8 in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 8. Nests of Quindina sanantonio sp. n. in the San Antonio Forest, Municipality of Santiago de Cali, Valle del Cauca, Colombia. (A) Nest #1, 29 October 2021. (B) Nest #1, 20 November 2021. (C) Nest #2. (D) Nest #3. (E) Nest #4. (F) Nest #5.
Figure 7 in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 7. (A) Trail in San Antonio Forest (Municipality of Santiago de Cali, Valle del Cauca, Colombia). (B–F) Location of Quindina sanantonio sp. n. nests (white arrows) in the San Antonio Forest (B) Nest #1. (C) Nest #2. (D) Nest #3. (E) Nest #4. (F) Nest #5.
Figure 3 in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 3. Quindina horologium sp. n. (A–E) Male holotype (MUSENUV-Ar-2229): (A) Habitus, dorsal view; (B) lateral view. (C) Left pedipalp, ventral view, trochanter to tarsus. (D) Leg I, tibia to tarsus in prolateral view. (E) Chelicera (hand, fixed and movable fingers). Scale bars = 1 mm.
Figure 11 in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 11. Distribution map of Quindina species in Colombia, including the new species described in this study. The geographical data were taken or georeferenced from Pinto-da-Rocha and Bragagnolo (2017) and Pinzón and Pinto-Da-Rocha (2020).
Subspecies and Distribution. V. v. vulpes Linnaeus, 1758 — N Europe (Scandinavia). V. v. abietorum Merriam, 1900 — SW Canada (Alberta & British Columbia). V. v. aegyptiacus Sonnini, 1816 — Egypt, Israel, and Lybia. V. v. alascensis Merriam, 1900 — Alaska and NW Canada (NW Territories & Yukon). V. v. alpheraky: Satunin, 1906 — Kazakhstan. V. v. anatolica Thomas, 1920 — Turkey. V. v. arabica Thomas, 1902 — Arabian peninsula. V. v. atlantica Wagner, 1841 — Algeria (forested Atlas Mts). V. v. bangsi Merriam, 1900 — NE Canada (Labrador). V. v. barbara Shaw, 1800 — NW Africa (Barbary Coast). V. v. beringiana Middendorff, 1875 — NE Siberia (shore of Bering Strait). V. v. cascadensis Merriam, 1900 — NW USA (Cascade Mountains, Oregon & Washington). V. v. caucasica Dinnik, 1914 — SW Russia (Caucasus). V. v. crucigera Bechstein, 1789 — Europe through N & C Russia. V. v. daurica Ognev, 1931 — E Russia (Amur, Siberia & Transbaikalia). V.v. deletrix Bangs, 1898 — NE Canada (Newfoundland). V. v. dolichocrania Ognev, 1926 — SE Siberia (S Ussuri). V. v. flavescens Gray, 1843 — N Iran. V. v. fulva Desmarest, 1820 — E USA. V. v. griffith: Blyth, 1854 — Afghanistan and N Pakistan. V.v. harrimani Merriam, 1900 — Alaska (Kodiak I). V. v. hoole Swinhoe, 1870 — S China (Fujian to Sichuan). V. v. ichnusae G. S. Miller, 1907 — Corsica and Sardinia. V. v. induta G. S. Miller, 1907 — Cyprus. V. v. jakutensis Ognev, 1923 — E Siberia (S of Yakutsk). V. v. japonica Gray, 1868 — Japan. V. v. karagan Erxleben, 1777 — Mongolia, Kazakhstan, and Kirgizstan. V. v. kenaiensis Merriam, 1900 — Alaska (Kenai Peninsula). V. v. kurdistanica Satunin, 1906 — Armenia and NE Turkey. V. v. macroura Baird, 1852 — USA (Mountain States). V. v. montana Pearson, 1836 — Himalayas form China (Yunnan) to C Pakistan. V. v. mecator Merriam, 1900 — SW USA (California & Nevada). V_ v. ochroxantha Ognev, 1926 — E Russian Turkestan, Aksai, Kirgizstan, Semirechie. V. v. palaestina Thomas, 1920 —Jordan and Lebanon. V.v. peculiosa Kishida, 1924 — Korea. V. v. pusilla Blyth, 1854 — NW India to Irak. V.v. regalis Merriam, 1900 — N Great Plains of Canada and USA. V. v. rubricosa Bangs, 1898 — E Canada. V.v. schrencki Kishida, 1924 — N Japan (Hokkaido) and NE Russia (Sakhalin). V. v. silacea G. S. Miller, 1907 — Iberian Peninsula. V.v. splendidissima Kishida, 1924 — E Russia (N & C Kurile Is). V. v. stepensis Brauner, 1914 — steppes of S Russia. V. v. tobolica Ognev, 1926 — Russia (lower basin of Ob River) V. v. tschiliensis Matschie, 1907 — NE China. Foxes of European origin were introduced into E USA and Canada in the 17" century, subsequently mixed with local subspecies. Also introduced to Australia in 1800s, and the Falkland Islands (Malvinas). in Canidae
Subspecies and Distribution. V. v. vulpes Linnaeus, 1758 — N Europe (Scandinavia). V. v. abietorum Merriam, 1900 — SW Canada (Alberta & British Columbia). V. v. aegyptiacus Sonnini, 1816 — Egypt, Israel, and Lybia. V. v. alascensis Merriam, 1900 — Alaska and NW Canada (NW Territories & Yukon). V. v. alpheraky: Satunin, 1906 — Kazakhstan. V. v. anatolica Thomas, 1920 — Turkey. V. v. arabica Thomas, 1902 — Arabian peninsula. V. v. atlantica Wagner, 1841 — Algeria (forested Atlas Mts). V. v. bangsi Merriam, 1900 — NE Canada (Labrador). V. v. barbara Shaw, 1800 — NW Africa (Barbary Coast). V. v. beringiana Middendorff, 1875 — NE Siberia (shore of Bering Strait). V. v. cascadensis Merriam, 1900 — NW USA (Cascade Mountains, Oregon & Washington). V. v. caucasica Dinnik, 1914 — SW Russia (Caucasus). V. v. crucigera Bechstein, 1789 — Europe through N & C Russia. V. v. daurica Ognev, 1931 — E Russia (Amur, Siberia & Transbaikalia). V.v. deletrix Bangs, 1898 — NE Canada (Newfoundland). V. v. dolichocrania Ognev, 1926 — SE Siberia (S Ussuri). V. v. flavescens Gray, 1843 — N Iran. V. v. fulva Desmarest, 1820 — E USA. V. v. griffith: Blyth, 1854 — Afghanistan and N Pakistan. V.v. harrimani Merriam, 1900 — Alaska (Kodiak I). V. v. hoole Swinhoe, 1870 — S China (Fujian to Sichuan). V. v. ichnusae G. S. Miller, 1907 — Corsica and Sardinia. V. v. induta G. S. Miller, 1907 — Cyprus. V. v. jakutensis Ognev, 1923 — E Siberia (S of Yakutsk). V. v. japonica Gray, 1868 — Japan. V. v. karagan Erxleben, 1777 — Mongolia, Kazakhstan, and Kirgizstan. V. v. kenaiensis Merriam, 1900 — Alaska (Kenai Peninsula). V. v. kurdistanica Satunin, 1906 — Armenia and NE Turkey. V. v. macroura Baird, 1852 — USA (Mountain States). V. v. montana Pearson, 1836 — Himalayas form China (Yunnan) to C Pakistan. V. v. mecator Merriam, 1900 — SW USA (California & Nevada). V_ v. ochroxantha Ognev, 1926 — E Russian Turkestan, Aksai, Kirgizstan, Semirechie. V. v. palaestina Thomas, 1920 —Jordan and Lebanon. V.v. peculiosa Kishida, 1924 — Korea. V. v. pusilla Blyth, 1854 — NW India to Irak. V.v. regalis Merriam, 1900 — N Great Plains of Canada and USA. V. v. rubricosa Bangs, 1898 — E Canada. V.v. schrencki Kishida, 1924 — N Japan (Hokkaido) and NE Russia (Sakhalin). V. v. silacea G. S. Miller, 1907 — Iberian Peninsula. V.v. splendidissima Kishida, 1924 — E Russia (N & C Kurile Is). V. v. stepensis Brauner, 1914 — steppes of S Russia. V. v. tobolica Ognev, 1926 — Russia (lower basin of Ob River) V. v. tschiliensis Matschie, 1907 — NE China. Foxes of European origin were introduced into E USA and Canada in the 17" century, subsequently mixed with local subspecies. Also introduced to Australia in 1800s, and the Falkland Islands (Malvinas).
Subspecies and Distribution. P. c. culpaeus Molina, 1782 — W & C Argentina and C Chile. P. ¢. andinus Thomas, 1914 — altiplano of Bolivia, N Chile, and Peru. Pc. lycoides Philippi, 1895 — Tierra del Fuego. Pc. magellanicus Gray, 1837 — Argentina and S Chile. P. c. reissu Hilzheimer, 1906 — Ecuadorian Andes and extreme S Colombia (Narino). P. c. smithersi Thomas, 1914 — Argentina (Cordoba Mts). in Canidae
Subspecies and Distribution. P. c. culpaeus Molina, 1782 — W & C Argentina and C Chile. P. ¢. andinus Thomas, 1914 — altiplano of Bolivia, N Chile, and Peru. Pc. lycoides Philippi, 1895 — Tierra del Fuego. Pc. magellanicus Gray, 1837 — Argentina and S Chile. P. c. reissu Hilzheimer, 1906 — Ecuadorian Andes and extreme S Colombia (Narino). P. c. smithersi Thomas, 1914 — Argentina (Cordoba Mts).
Subspecies and Distribution. H. e. edwardsii Geoffroy Saint-Hilaire, 1818 — SE India and Sri Lanka. H. e. carnaticus Wroughton, 1921 — SW India (Karnatka). H. e. moerens Wroughton, 1915 — Bangladesh, Bhutan, C & NE India, and Nepal. H. e. montanus Bechthold, 1936 — Saudi Arabia to NW India. H. e. pallens Ryley, 1914 — W India (Gujarat). A few old museum specimens are reported from Peninsular Malaysia, whereit is said to have been introduced, butit has not been recorded there since the beginning of the 20" century. in Herpestidae
Subspecies and Distribution. H. e. edwardsii Geoffroy Saint-Hilaire, 1818 — SE India and Sri Lanka. H. e. carnaticus Wroughton, 1921 — SW India (Karnatka). H. e. moerens Wroughton, 1915 — Bangladesh, Bhutan, C & NE India, and Nepal. H. e. montanus Bechthold, 1936 — Saudi Arabia to NW India. H. e. pallens Ryley, 1914 — W India (Gujarat). A few old museum specimens are reported from Peninsular Malaysia, whereit is said to have been introduced, butit has not been recorded there since the beginning of the 20" century.
Subspecies and Distribution. U. a. arctos Linnaeus, 1758 — Europe and W Russia. U. a. alascensis Merriam, 1896 — most of Alaska (excluding Alaska Peninsula, SE panhandle & Kodiak Island group). U. a. beringianus Middendorff, 1853 — NE Russia (Kamchatka Peninsula & N Kuril Islands northward through the Koryak Autonomous District, and along W coast of the Sea of Okhotsk). U. a. collaris Cuvier, 1824 — Russia (Siberia, from E of the Yenisey River to the Bering Sea, but excluding Kamchatka and more southern parts of the Russian Far East), N Mongolia. U. a. dalli Merriam, 1896 — SE Alaska (N of Alexander Archipelago). U. a. gyas Merriam, 1902 — Alaska peninsula. U. a. horribilis Ord, 1815 —W Canada (Yukon, North-West Territories, British Columbia & Alberta), inland W USA (extirpated from S Wyoming to Mexico). U. a. isabellinus Horsfield, 1826 — N India, Pakistan, Afghanistan, N to Kazakhstan and Mongolia (Gobi Desert). U. a. lasiotus Gray, 1867 — Russia (Southern Kuril Islands, Sakhalin, Ussuri/Amur river region of the Russian Far East), NE China, North Korea, and Japan (Hokkaido). U. a. middendorffi Merriam, 1896 — Alaska (Kodiak Island & nearby islands). U. a. pruinosus Blyth, 1853 — Tibetan Plateau, China, N Nepal. U. a. sitkensis Merriam, 1896 — SE Alaska (Alexander Archipelago & adjacent coastal area). U. a. stikeenensis Merriam, 1914 — W Canada (W British Columbia), and formerly W USA (W Washington and Oregon). U. a. syriacus Hemprich & Ehrenberg, 1828 — Middle East, from Turkey to Iran (extirpated in Syria), Caucasus mountains of Russia, Georgia, Armenia and Azerbaijan. in Ursidae
Subspecies and Distribution. U. a. arctos Linnaeus, 1758 — Europe and W Russia. U. a. alascensis Merriam, 1896 — most of Alaska (excluding Alaska Peninsula, SE panhandle & Kodiak Island group). U. a. beringianus Middendorff, 1853 — NE Russia (Kamchatka Peninsula & N Kuril Islands northward through the Koryak Autonomous District, and along W coast of the Sea of Okhotsk). U. a. collaris Cuvier, 1824 — Russia (Siberia, from E of the Yenisey River to the Bering Sea, but excluding Kamchatka and more southern parts of the Russian Far East), N Mongolia. U. a. dalli Merriam, 1896 — SE Alaska (N of Alexander Archipelago). U. a. gyas Merriam, 1902 — Alaska peninsula. U. a. horribilis Ord, 1815 —W Canada (Yukon, North-West Territories, British Columbia & Alberta), inland W USA (extirpated from S Wyoming to Mexico). U. a. isabellinus Horsfield, 1826 — N India, Pakistan, Afghanistan, N to Kazakhstan and Mongolia (Gobi Desert). U. a. lasiotus Gray, 1867 — Russia (Southern Kuril Islands, Sakhalin, Ussuri/Amur river region of the Russian Far East), NE China, North Korea, and Japan (Hokkaido). U. a. middendorffi Merriam, 1896 — Alaska (Kodiak Island & nearby islands). U. a. pruinosus Blyth, 1853 — Tibetan Plateau, China, N Nepal. U. a. sitkensis Merriam, 1896 — SE Alaska (Alexander Archipelago & adjacent coastal area). U. a. stikeenensis Merriam, 1914 — W Canada (W British Columbia), and formerly W USA (W Washington and Oregon). U. a. syriacus Hemprich & Ehrenberg, 1828 — Middle East, from Turkey to Iran (extirpated in Syria), Caucasus mountains of Russia, Georgia, Armenia and Azerbaijan.
Subspecies and Distribution. P.l. lotor Linnaeus, 1758 — NE USA. P.l. auspicatus Nelson, 1930 — SE USA (Central Florida Keys). P. l. elucus Bangs, 1898 — SE USA (Florida). P. l. excelsus Nelson & Goldman, 1930 — NW USA (in and near Idaho). P.l. fuscipes Mearns, 1914 —S USA (Texas) and NE Mexico (Tamaulipas, Coahuila). P.l. grinnelli Nelson & Goldman, 1930 — Mexico (S Baja California). P. l. hernandezii Wagler, 1831 — Mexico. P.l. hirtus Nelson & Goldman, 1930 — Central Plains of USA and Canada. P. l. incautus Nelson, 1930 — SE USA (W Florida Keys). P. l. inesperatus Nelson, 1930 — SE USA (E Florida Keys). P. l. insularis Merriam, 1898 — W Mexico (Maria Madre I). P.l. litoreus Nelson & Goldman, 1930 — E USA (coastal Georgia). P. l. marinus Nelson, 1930 — SE USA (Florida Everglades). P. l. megalodous Lowery, 1943 — S USA (coastal Louisiana). P.l. pacificus Merriam, 1899 — NW USA. P. l. pallidus Merriam, 1900 — SW USA. P. l. psora Gray, 1842 — SW USA (California). P.l. pumilus G.S. Miller, 1911 — Central America. P. l. simus Gidley, 1906 — W USA (N California). P. l. vancouverensis Nelson & Goldman, 1930 — SW Canada (Vancouver I). in Procyonidae
Subspecies and Distribution. P.l. lotor Linnaeus, 1758 — NE USA. P.l. auspicatus Nelson, 1930 — SE USA (Central Florida Keys). P. l. elucus Bangs, 1898 — SE USA (Florida). P. l. excelsus Nelson & Goldman, 1930 — NW USA (in and near Idaho). P.l. fuscipes Mearns, 1914 —S USA (Texas) and NE Mexico (Tamaulipas, Coahuila). P.l. grinnelli Nelson & Goldman, 1930 — Mexico (S Baja California). P. l. hernandezii Wagler, 1831 — Mexico. P.l. hirtus Nelson & Goldman, 1930 — Central Plains of USA and Canada. P. l. incautus Nelson, 1930 — SE USA (W Florida Keys). P. l. inesperatus Nelson, 1930 — SE USA (E Florida Keys). P. l. insularis Merriam, 1898 — W Mexico (Maria Madre I). P.l. litoreus Nelson & Goldman, 1930 — E USA (coastal Georgia). P. l. marinus Nelson, 1930 — SE USA (Florida Everglades). P. l. megalodous Lowery, 1943 — S USA (coastal Louisiana). P.l. pacificus Merriam, 1899 — NW USA. P. l. pallidus Merriam, 1900 — SW USA. P. l. psora Gray, 1842 — SW USA (California). P.l. pumilus G.S. Miller, 1911 — Central America. P. l. simus Gidley, 1906 — W USA (N California). P. l. vancouverensis Nelson & Goldman, 1930 — SW Canada (Vancouver I).
Subspecies and Distribution. H.a.amphibiusLinnaeus,1758—sub-SaharanAfrica,exceptasbelow. H.a.capensisDesmoulins,1825—ZambiaStoSouthAfrica. H. a. kiboko Heller, 1914 — Kenya and Somalia. in Hippopotamidae
Subspecies and Distribution. H.a.amphibiusLinnaeus,1758—sub-SaharanAfrica,exceptasbelow. H.a.capensisDesmoulins,1825—ZambiaStoSouthAfrica. H. a. kiboko Heller, 1914 — Kenya and Somalia.
FIGURE 11. Pulvinaria photiniae Kuwana, 1914 in Redescriptions of six Japanese species of the genus Pulvinaria (Hemiptera: Coccomorpha: Coccidae) with four new synonymies
FIGURE 11. Pulvinaria photiniae Kuwana, 1914, adult female collected from Chiba prefecture, Japan in 2001. ANT, antenna; AP, anal plate; DA, dermal areolation; DMD, dorsal microduct; DS, dorsal seta; DTD, dorsal tubular duct; LG, leg; MP, multilocular pores; MS, marginal seta; POP, preopercular pores; SDP, spiracular disc pore; SSP, stigmatic spines; VMD, ventral microduct; VTD, ventral tubular ducts, types I to III. Scale bars: 200 μm for ANT and LG; 100 μm for AP and DA; 50 μm for MS and SSP; 10 μm for all other features.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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