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Figs. 1-8 – 1 in Notes on Longitarsus aphthonoides Weise 1887 and on the species groups of L. lateripunctatus (Rosenhauer 1856) and L. curtus (Allard 1860) (Coleoptera, Chrysomelidae)

Figs. 1-8 – 1) L. aphthonoides. Wroclaw Wojnów. 2) L. aphthonoides. Chabarofka: paralectotypes. 3) L. callidus. Talysch Mountains: holotype. 4) L. callidus, holotype: aedeagus. 5) L. personatus. Budapest. 6) L. lateripunctatus. Promontorio del Gargano. 7) L. monticola. Monte Grigna Settentrionale. 8) L. curtus. Bisamberg. (Photos / Foto: 1, 3-8: S. Zoia; 2: L. Behne).

Figs. 23-30 in Notes on Longitarsus aphthonoides Weise 1887 and on the species groups of L. lateripunctatus (Rosenhauer 1856) and L. curtus (Allard 1860) (Coleoptera, Chrysomelidae)

Figs. 23-30 – Aedeagus: median lobe / lobo mediano: a) ventral view / vista ventrale; b) lateral view / vista laterale. 23-26) L. lateripunctatus. 27-30) L. personatus. Localities / Località: 23) Algeciras; 24) Tunisi; 25) Giglio island; 26) Marina di Modica; 27) Peretola; 28, Trieste; 29-30) Krems.

Figs. 13-22 – Spermatheca. 13-17 in Notes on Longitarsus aphthonoides Weise 1887 and on the species groups of L. lateripunctatus (Rosenhauer 1856) and L. curtus (Allard 1860) (Coleoptera, Chrysomelidae)

Figs. 13-22 – Spermatheca. 13-17) L. lateripunctatus. 18-22) L. personatus. Localities / Località: 13) Laigueglia; 14) Talamone; 15) Circummarpiccolo; 16) Monti Peloritani; 17) Corfù, Valle di Ropa; 18) Corfù; 19) Messina, San Pier Niceto; 20) Fiume Lato; 21) Riano; 22) Sant'Ilario Ligure.

Fig. 44 in Notes on Longitarsus aphthonoides Weise 1887 and on the species groups of L. lateripunctatus (Rosenhauer 1856) and L. curtus (Allard 1860) (Coleoptera, Chrysomelidae)

Fig. 44 – Italian distribution of L. monticola and L. curtus. / Distribuzione italiana di L. monticola e L. curtus.

Рис. 2. UPGMA-ΑенΑрограмма схоΑства виΑового состава (А) и фаунистическая структура (B) сообществ земΛероек в пяти ΛокаΛитетах Амурской обΛасти: ЗЗ — Зейский заповеΑник; НЗ — Норский заповеΑник; ХЗ — Хинганский заповеΑник; ЧФЗ — ХинганоАрхаринский заказник; НБС — территория зоны вΛияния Нижнебурейской ГЭС. ΔТФ — Αревнетаежная фауна; БФ — бореаΛьная фауна; НФ — немораΛьная фауна; Αр. — преΑставитеΛи Αругих фауногенетических группировок (пояснения в тексте) Fig. 2. UPGMA dendrogram of species composition similarity (A) and fauna structure (B) of shrew communities in five Amur region localities: ZZ — Zeya nature reserve; NZ — Norsky nature reserve; KhZ — Khingansky nature reserve; ChFZ — KhinganoArkharinsky nature reserve; NBS — the area influenced by the Nizhnebureyskaya hydroelectric power station. DTP — ancient taiga fauna; BF — boreal fauna; NF — nemoral fauna; others — representatives of other faunagenetic groups (explained in the text) in Shrew species composition and fauna structure in the Norsky reserve

Рис. 2. UPGMA-ΑенΑрограмма схоΑства виΑового состава (А) и фаунистическая структура (B) сообществ земΛероек в пяти ΛокаΛитетах Амурской обΛасти: ЗЗ — Зейский заповеΑник; НЗ — Норский заповеΑник; ХЗ — Хинганский заповеΑник; ЧФЗ — ХинганоАрхаринский заказник; НБС — территория зоны вΛияния Нижнебурейской ГЭС. ΔТФ — Αревнетаежная фауна; БФ — бореаΛьная фауна; НФ — немораΛьная фауна; Αр. — преΑставитеΛи Αругих фауногенетических группировок (пояснения в тексте) Fig. 2. UPGMA dendrogram of species composition similarity (A) and fauna structure (B) of shrew communities in five Amur region localities: ZZ — Zeya nature reserve; NZ — Norsky nature reserve; KhZ — Khingansky nature reserve; ChFZ — KhinganoArkharinsky nature reserve; NBS — the area influenced by the Nizhnebureyskaya hydroelectric power station. DTP — ancient taiga fauna; BF — boreal fauna; NF — nemoral fauna; others — representatives of other faunagenetic groups (explained in the text)

Рис. 2. Gynaephora (rossii): 1 — гусеницa в прироΔной среΔе (фото Е. И. Троевой); 2 — коконы; биотопы виΔа: 3 — в устье р. Энюмчувеем; 4 — на острове Крестовский (фото автора) Fig. 2. Gynaephora (rossii): 1 — larva in the natural environment (photo by Elena I. Troeva); 2 — cocoons; species biotopes: 3 — at the mouth of the Enumchuveem river; 4 — on Krestovsky island (photo of the author) in New data on the distribution of the Gynaephora (rossii) species group in Northern Yakutia

Рис. 2. Gynaephora (rossii): 1 — гусеницa в прироΔной среΔе (фото Е. И. Троевой); 2 — коконы; биотопы виΔа: 3 — в устье р. Энюмчувеем; 4 — на острове Крестовский (фото автора) Fig. 2. Gynaephora (rossii): 1 — larva in the natural environment (photo by Elena I. Troeva); 2 — cocoons; species biotopes: 3 — at the mouth of the Enumchuveem river; 4 — on Krestovsky island (photo of the author)

Рис. 1. Карта-схема пунктов сборов Gynaephora (rossii) в Якутии: 1 — о-в КотеΛьный; 2 — о-в СтоΛбовой; 3 — о-в МаΛый Αяховский; 4 — о-в БоΛьшой Αяховский; 5 — п-ов Быковский в устье Αены; 6 — СеΛΛяхская губа, р. СеΛях, низовья Яны; 7 — КоΛымская протока, низовья ИнΔигирки; 8 — озеро ХомоΛох, бассейн р. БёрёΛёх, низовья ИнΔигирки; 9 — о-в Крестовский; 10 — о-в ЧетырехстоΛбовой; 11 — устье р. Энюмчувеем, южное побережье Восточно-Сибирского моря; 12 — хребет СунтарХаята; 13 — р. ÀжеΛинΔа в системе Станового хребта (точками обозначены ранее опубΛикованные точки, треугоΛьниками — новые местообитания) Fig. 1. Chart of Gynaephora (rossii) collection sites in Yakutia: 1 — Kotelny island; 2 — Stolbovoy island; 3 — Maly Lyakhovsky island; 4 — Bolshoi Lyakhovsky island; 5 — Bykovsky peninsula at the mouth of the Lena river; 6 — Sellakhskaya bay, Selyakh river, lower reaches of the Yana river; 7 — Kolymskaya channel, lower reaches of the Indigirka river; 8 — Lake Homolokh, Berelekh river basin, lower reaches of the Indigirka river; 9 — Krestovsky island; 10 — Chetyrekhstolbovoy island; 11 — the mouth of the Enyumchuveem river, southern coast of the East Siberian sea; 12 — Suntar-Khayata ridge; 13 — Gelinda river in the Stanovoy ridge system (dots indicate previously published localities, triangles indicate new localities) in New data on the distribution of the Gynaephora (rossii) species group in Northern Yakutia

Рис. 1. Карта-схема пунктов сборов Gynaephora (rossii) в Якутии: 1 — о-в КотеΛьный; 2 — о-в СтоΛбовой; 3 — о-в МаΛый Αяховский; 4 — о-в БоΛьшой Αяховский; 5 — п-ов Быковский в устье Αены; 6 — СеΛΛяхская губа, р. СеΛях, низовья Яны; 7 — КоΛымская протока, низовья ИнΔигирки; 8 — озеро ХомоΛох, бассейн р. БёрёΛёх, низовья ИнΔигирки; 9 — о-в Крестовский; 10 — о-в ЧетырехстоΛбовой; 11 — устье р. Энюмчувеем, южное побережье Восточно-Сибирского моря; 12 — хребет СунтарХаята; 13 — р. ÀжеΛинΔа в системе Станового хребта (точками обозначены ранее опубΛикованные точки, треугоΛьниками — новые местообитания) Fig. 1. Chart of Gynaephora (rossii) collection sites in Yakutia: 1 — Kotelny island; 2 — Stolbovoy island; 3 — Maly Lyakhovsky island; 4 — Bolshoi Lyakhovsky island; 5 — Bykovsky peninsula at the mouth of the Lena river; 6 — Sellakhskaya bay, Selyakh river, lower reaches of the Yana river; 7 — Kolymskaya channel, lower reaches of the Indigirka river; 8 — Lake Homolokh, Berelekh river basin, lower reaches of the Indigirka river; 9 — Krestovsky island; 10 — Chetyrekhstolbovoy island; 11 — the mouth of the Enyumchuveem river, southern coast of the East Siberian sea; 12 — Suntar-Khayata ridge; 13 — Gelinda river in the Stanovoy ridge system (dots indicate previously published localities, triangles indicate new localities)

Figs 10–22 in Four new species of sanguinolenta-group of the genus Macrophya (Hymenoptera: Tenthredinidae) from China

Figs 10–22. Macrophya yichangensis sp. nov. 10. Adult female, dorsal view. 11. Adult male, dorsal view. 12. Female head, dorsal view. 13. Female head, front view. 14. Female antenna. 15. Female mesopleuron and metapleuron. 16. Ovipositor sheath, lateral view. 17. Male head, front view. 18. Male head. 19. Lancet. 20. The 8th–10th serrulae of lancet. 21. Gonoforceps. 22. Penis valve. Scale bars: 10–11 = 1 mm, 17, 21 = 100 μm, 18, 22 = 50 μm.

Figs 1–9 in Four new species of sanguinolenta-group of the genus Macrophya (Hymenoptera: Tenthredinidae) from China

Figs 1–9. Macrophya cheni sp. nov. 1. Adult female, dorsal view. 2. Female head, dorsal view. 3. Female head, front view. 4. Female antenna. 5. Female mesopleuron and metapleuron. 6. Female hind tibia and tarsus, lateral view. 7. Ovipositor sheath, lateral view. 8. Lancet. 9. The 8th–10th serrulae of lancet. Scale bars: 1 = 1 mm, 8 = 100 μm, 9 = 50 μm.

Figs 31–42 in Four new species of sanguinolenta-group of the genus Macrophya (Hymenoptera: Tenthredinidae) from China

Figs 31–42. Macrophya reni sp. nov. 31. Adult female, dorsal view. 32. Adult male, dorsal view. 33. Female head, dorsal view. 34. Female head, front view. 35. Female mesopleuron and metapleuron. 36. Ovipositor sheath, lateral view. 37. Male head, front view. 38. Male antenna. 39. Lancet. 40. The 8th–10th serrulae of lancet. 41. Gonoforceps. 42. Penis valve. Scale bars: 31–32 = 1 mm, 39, 41 = 100 μm, 40, 42 = 50 μm.

Figs 23–30 in Four new species of sanguinolenta-group of the genus Macrophya (Hymenoptera: Tenthredinidae) from China

Figs 23–30. Macrophya elegansoma sp. nov. 23. Adult female, dorsal view. 24. Female head, dorsal view. 25. Female Head, front view. 26. Female antenna. 27. Female mesopleuron and metapleuron. 28. Ovipositor sheath, lateral view. 29. Lancet. 30. The 8th–10th serrulae of lanmcet. Scale bars: 23 = 1 mm, 29 = 100 μm, 30 = 50 μm.

Fig. 14 in New data to the earthworm fauna of the Korean Peninsula with redescription of Eisenia koreana (Zicsi) and remarks on the Eisenia nordenskioldi species group (Oligochaeta, Lumbricidae)

Fig. 14. Bayesian inference tree of the Asian Eisenia species using COI1 sequenes. Numbers above branches indicate Bayesian posterior probabilities.

Fig. 13 in New data to the earthworm fauna of the Korean Peninsula with redescription of Eisenia koreana (Zicsi) and remarks on the Eisenia nordenskioldi species group (Oligochaeta, Lumbricidae)

Fig. 13. Maximum Likelihood tree of the Asian Eisenia species using COI1 sequenes. Numbers above branches indicate ML bootstrap support.

Fig. 12 in New data to the earthworm fauna of the Korean Peninsula with redescription of Eisenia koreana (Zicsi) and remarks on the Eisenia nordenskioldi species group (Oligochaeta, Lumbricidae)

Fig. 12. Eisenia sp. setal arrangement. aa = distance between the ventral setal lines, ab = distance between the ventrolateral setal lines, cd = distance between the dorsolateral setal lines, dd = distance between the dorsal setal lines.

Fig. 11 in New data to the earthworm fauna of the Korean Peninsula with redescription of Eisenia koreana (Zicsi) and remarks on the Eisenia nordenskioldi species group (Oligochaeta, Lumbricidae)

Fig. 11. Eisenia lagodechiensis (Michaelsen, 1910) setal arrangement. aa = distance between the ventral setal lines, ab = distance between the ventrolateral setal lines, cd = distance between the dorsolateral setal lines, dd = distance between the dorsal setal lines.

Fig. 10 in New data to the earthworm fauna of the Korean Peninsula with redescription of Eisenia koreana (Zicsi) and remarks on the Eisenia nordenskioldi species group (Oligochaeta, Lumbricidae)

Fig. 10. Eisenia nordenskioldi nordenskioldi (Eisen, 1879) setal arrangement. aa = distance between the ventral setal lines, ab = distance between the ventrolateral setal lines, cd = distance between the dorsolateral setal lines, dd = distance between the dorsal setal lines.

Fig. 8 in New data to the earthworm fauna of the Korean Peninsula with redescription of Eisenia koreana (Zicsi) and remarks on the Eisenia nordenskioldi species group (Oligochaeta, Lumbricidae)

Fig. 8. Eisenia nordenskioldi cf. pallida Malevic, 1956; setal arrangement of the Korean specimens. aa = distance between the ventral setal lines, ab = distance between the ventrolateral setal lines, cd = distance between the dorsolateral setal lines, dd = distance between the dorsal setal lines.

Fig. 3 in New data to the earthworm fauna of the Korean Peninsula with redescription of Eisenia koreana (Zicsi) and remarks on the Eisenia nordenskioldi species group (Oligochaeta, Lumbricidae)

Fig. 3. Eisenia koreana (Zicsi, 1972) setal arrangement. aa = distance between the ventral setal lines, ab = distance between the ventrolateral setal lines, cd = distance between the dorsolateral setal lines, dd = distance between the dorsal setal lines.

Fig. 6. Strict consensus tree resulting from 20 in A new species of Afrolaophonte (Copepoda, Harpacticoida, Laophontidae) from Korea and cladistic tests of species-groups

Fig. 6. Strict consensus tree resulting from 20 equally parsimonious trees from an analysis of 15 weighted morphological characters (Table 1) for 13 species of Afrolaophonte Chappuis, 1960 and one outgroup, Arenolaophonte stygia Lang, 1965. Characters 0, 2-4, and 11-14 were down-weighted to 0.5, while others were left at the default weight of 1. Full circles represent presumed synapomorphies, empty circles presumed plesiomorphies or homoplasies, Arabic numerals above circles characters, and Arabic numerals below circles character states.

Fig. 5 in A new species of Afrolaophonte (Copepoda, Harpacticoida, Laophontidae) from Korea and cladistic tests of species-groups

Fig. 5. Two out of 12 equally parsimonious trees resulting from an analysis of 15 unweighted morphological characters (Table 1) scored for 13 species of Afrolaophonte Chappuis, 1960 and one outgroup, Arenolaophonte stygia Lang, 1965. The trees were constructed using Winclada/NONA and heuristic search method. Full circles represent presumed synapomorphies, empty circles presumed plesiomorphies or homoplasies, Arabic numerals above circles characters, Arabic numerals below circles character states, and Roman numerals indicate species-groups proposed by Fiers (1990). Afrolaophonte aequatorialis Cottarelli and Mura, 1981 has a basal position in six trees (as in A) and terminal position in six trees (as in B).