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FIGURE 7 in New or amended data on Mediterranean Amphipoda: genera Dexamine, Ericthonius and Stenothoe

FIGURE 7. Ericthonius didymus sp. n. Gn2 m = another second male gnathopod; P3–6 = peraeopods 3–6 in situ; P3, 4 = peraeopod 3, 4 in detail; Cx 5 f = coxa 5 female; P5 m = coxa 5 and peraeopod 5 of male; P5 f = peraeopod 5 of female.

FIGURE 6 in New or amended data on Mediterranean Amphipoda: genera Dexamine, Ericthonius and Stenothoe

FIGURE 6. Ericthonius didymus sp. n. Mxp + Gn1 = maxilliped and first gnathopod in situ; Gn2 f = female second gnathopod; Gn1 m, Gn2 m = first and second male gnathopod.

FIGURE 10. Stenothoe dollfusi Chevreux, 1887 in New or amended data on Mediterranean Amphipoda: genera Dexamine, Ericthonius and Stenothoe

FIGURE 10. Stenothoe dollfusi Chevreux, 1887: Gn2 male, female = second gnathopod of both sexes; P7 = peraeopod 7; U2, 3 = uropod 2, 3 of both sexes; T = telson.

FIGURE 5 in New or amended data on Mediterranean Amphipoda: genera Dexamine, Ericthonius and Stenothoe

FIGURE 5. Ericthonius didymus sp. n. A1, 2 = antennae; Hd = head; Mx1, 2 = maxillae; LL = lower lip; Md = mandible, Md' = mandible enlarged; Mxp = maxilliped, Mxp' = other maxilliped.

Figure 6 in Karyotypes of water scavenger beetles (Coleoptera: Hydrophilidae): new data and review of published records

Figure 6. Karyotypes of the Hydrophilini. A–C, Hydrophilus, mitotic karyotype from embryo (A–B, Hydrophilus piceus; C, Hydrophilus pistaceus). D–H, Hydrochara: (D–F) Hydrochara caraboides, mitotic karyotype, embryo; (G–H) Hydrochara flavipes, mitotic karyotype, midgut. I–J, Sternolophus solieri (I, male mitotic karyotype; J, meiotic first metaphase from testes). A, C, D, G, I, without treatment. B, E, F, H, C-banded. Habitus figures: (K) Sternolophus solieri; (L) Hydrochara caraboides; (M) Hydrophilus piceus, from Short & Fikáček (2013).

Figure 5 in Karyotypes of water scavenger beetles (Coleoptera: Hydrophilidae): new data and review of published records

Figure 5. Karyotypes of the Hydrobiusini. A–D, Limnohydrobius convexus: (A–B) mitosis, midgut; (C–D): testis, prometaphase. F–J, Limnoxenus niger: (F–H) midgut; (I–J) meiotic metaphase I, testes. A–C, E–F, I, without treatment. D, G, H, J, C-banded. Habitus figures: (E) Limnohydrobius convexus; (K) Limnoxenus niger.

Figure 3 in Karyotypes of water scavenger beetles (Coleoptera: Hydrophilidae): new data and review of published records

Figure 3. Karyotypes of the Laccobiini, without treatment. A–H, Paracymus: (A–B) Paracymus aeneus, mitotic metaphase from midgut; (C–D) Paracymus scutellaris (C, spermatogonial mitosis, metaphase; D, mitotic metaphase from midgut.); (E–G) meiotic metaphase I from testes (E, Paracymus aeneus; F–G, Paracymus scutellaris). I–M, Tormus, mitotic metaphase from midgut: (I, K) Tormus posticalis; (J, L) Tormus helmsi. Habitus figures: (G) Paracymus scutellaris; (M) Tormus helmsi, from Fikáček et al. (2013).

Figure 1 in Karyotypes of water scavenger beetles (Coleoptera: Hydrophilidae): new data and review of published records

Figure 1. Tissues of hydrophiloid beetles used for chromosome preparations (as dissected, without any additional treatment, (B–E) in dorsal view; (A) Helophorus grandis; (B, C, I) Laccobius bipunctatus; (D–H) Coelostoma orbiculare). A, egg with a developing embryo. B–C, internal organs of the same male specimen in translucent light (B) and on black background (C). D, internal organs of a female with digestive system pulled aside. E, internal organs of male specimen. F, details of ovarioles and associated accessory glands. G–I, detail of midgut structure on black background (G) and in translucent light (H, I). Abbreviations: accg, accessory glands; aed, aedeagus; hg, hindgut; mg, midgut; Mt, Malpighian tubes; oo, ovarioles; ovi, ovipositor; rc, regeneration crypts; tes, testes. Not to scale.

Figure 2 in Karyotypes of water scavenger beetles (Coleoptera: Hydrophilidae): new data and review of published records

Figure 2. Karyotypes of the Amphiopini and Laccobiini. A–E, Amphiops mater, mitotic methaphase from midgut. F–L, Laccobius decorus, mitotic metaphase from midgut. A, C, F, H, J, without treatment. B, D, G, I, K, C-banded. Habitus figures: (E) Amphiops mater; (L) Laccobius decorus.

FIGURE 5 in Description of Electrogena sartorii sp. nov., a new representative of the genus Electrogena Zurwerra & Tomka, 1985 (Ephemeroptera: Heptageniidae), from Iran using molecular and morphological data

FIGURE 5. Setae and spines on hind tibia of Anapos kugleri. Abbreviations: orhs: outer row of hair-like setae; orss: outer row of spine-like setae; mrhs: middle row of hair-like setae; mrss: middle row of spine-like setae.

FIGURE 4. Electrogena gibedede, a in Description of Electrogena sartorii sp. nov., a new representative of the genus Electrogena Zurwerra & Tomka, 1985 (Ephemeroptera: Heptageniidae), from Iran using molecular and morphological data

FIGURE 4. Electrogena gibedede, a, first gill; b, seven gill; c, pronotum; d, bristles on the dorsal face of femora; e, glossae and paraglossae.

FIGURES 44–53 in New data on the wolf spiders from theAcantholycosa-complex (Araneae: Lycosidae) from the South Siberia

FIGURES 44–53. Tegulum and subtegulum (44–45, 52–53), bulb (46–48) and embolic division (49–51) of Acantholycosa sergeevi sp. n. (44–45) and Mongolicosa lizae sp. n. (46–53). 44, 46, 49, 52—ventral; 45, 47, 50, 53—anterior; 48, 51— retrolateral. Scale bars=0.2 mm. Abbreviations: Aa apical arm of the tegular apophysis, Ba basal arm of the tegular apophysis, Em embolus, Pl palea, Sd sperm duct, Ta terminal apophysis, Tg tegular apophysis.

FIGURES 10–19 in New data on the wolf spiders from theAcantholycosa-complex (Araneae: Lycosidae) from the South Siberia

FIGURES 10–19. Male palp (10–13) and bulb (14–19) of Acantholycosa sergeevi sp. n. (10–11), A. sayanensis (14–15), A. sidorovi sp. n. (16–17), A. levinae (18-19) and Mongolicosa lizae sp. n. (12–13). 10, 12—retrolateral; 11, 13, 14, 16, 18— ventral; 15, 17, 19—anterior. Scale bars=0.2 mm.

FIGURES 54–62 in New data on the wolf spiders from theAcantholycosa-complex (Araneae: Lycosidae) from the South Siberia

FIGURES 54–62. Epigyne and female internal genitalia of Acantholycosa sayanensis (54–56), A. azyuzini (57–59) and A. sidorovi sp. n. (60–62). 54, 57, 60—intact, ventral; 55, 58, 61—macerated, ventral; 56, 59, 62—macerated, dorsal. Scale bars=0.2 mm. Abbreviations: Ap apical pocket, Cd copulatory ducts, Fo epigynal fovea, Li lip of the epigyne, Re receptacle, Sb septal base, Ss septal stem.

FIGURES 72–77 in New data on the wolf spiders from theAcantholycosa-complex (Araneae: Lycosidae) from the South Siberia

FIGURES 72–77. Male of Acantholycosa sayanensis from Borus Mt. Range (72), female of Acantholycosa sp. (A. azyuzini or A. levinae) with egg sac, from Katunskyi Mt. Range (73), habitat of A. sayanensis and A. sergeevi sp. n. in Borus Mt. Range (74), collecting localities of studied species from the Acantholycosa-complex (75–76) and map showing the main mountain systems of South Siberia and adjacent regions (77). Diamond—A. sayanensis, square—A. sidorovi sp. n., triangle—A. kulikovi sp. n., star—A. levinae, circle—A. sergeevi sp. n., inverted triangle—Mongolicosa lizae sp. n. The frame of Fig. 76 refers to the content of Fig. 75.

FIGURES 32–43 in New data on the wolf spiders from theAcantholycosa-complex (Araneae: Lycosidae) from the South Siberia

FIGURES 32–43. Tegulum and subtegulum (32–37), bulb (38–40) and embolic division (41–43) of Acantholycosa sayanensis (32–33), A. sidorovi sp. n. (34–35), A. levinae (36–37) and A. sergeevi sp. n. (38–43). 32, 34, 36, 38, 41—ventral; 33, 35, 37, 39, 42—anterior; 40, 43—retrolateral. Scale bars=0.2 mm. Abbreviations: Aa apical arm of the tegular apophysis, Ba basal arm of the tegular apophysis, Em embolus, Pe extension of the palea, Pl palea, Ta terminal apophysis, Tg tegular apophysis, Ts triangle-shaped projection of the palea.

FIGURES 63–71 in New data on the wolf spiders from theAcantholycosa-complex (Araneae: Lycosidae) from the South Siberia

FIGURES 63–71. Epigyne and female internal genitalia of Acantholycosa kulikovi sp. n. (63–65), A. levinae (66–68) and Mongolicosa lizae sp. n. (69–71). 63, 66, 69—intact, ventral; 64, 67, 70—macerated, ventral; 65, 68, 71—macerated, dorsal. Scale bars=0.2 mm. Abbreviations: Al apical lips of the epigyne, Ap apical pocket, Cd copulatory ducts, Fo epigynal fovea, Li lip of the epigyne, Re receptacle, Sa septal base arm, Sb septal base, Ss septal stem.

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FIG. 9 in Two new sympatric water-mites (Acari: Hydrachnidia: Unionicolidae) from the mutelid bivalve Aspatharia sinuata (von Martens) in Nigeria with some data on unionicoline-bivalve relationships

FIG. 9. Unionicola (Mutelicola) planicurvata female, Prep. 1369, allotype. (a) Dorsal surface; (b) ventral surface; (c) genital Želd; (d) left palp; (e) right palp.

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FIG. 10 in Two new sympatric water-mites (Acari: Hydrachnidia: Unionicolidae) from the mutelid bivalve Aspatharia sinuata (von Martens) in Nigeria with some data on unionicoline-bivalve relationships

FIG. 10. Unionicola (Mutelicola) planicurvata. (a) Genital Želd, female, Prep. 1370; (b) left palp, female, Prep. 1370; (c) right palp, female, Prep. 1370; (d) left palp, female, Prep. 1368; (e) right palp, female, Prep. 1368; (f) PV of left palp, inner lateral face, female, Prep. 1368; (g) PV of left palp, outer lateral face, female, Prep. 1368.