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Рис. 3. Находки Arion subfuscus в восточной АЗии: 1–3 – Китай, по: Wiktor et al. [2000]; 4 – Приморский край у г. Фокино, по: ПроЗорова, Фоменко [2015]; 5, 6 – Курильские острова, Шикотан и Зеленый, по: ПроЗорова [2000, 2002]; 7 – г. Петропавловск-Камчатский. in Distribution of an invasive slug, Arion subfuscus (Draparnaud, 1805) in East Asia from Kamchatka to China

Рис. 3. Находки Arion subfuscus в восточной АЗии: 1–3 – Китай, по: Wiktor et al. [2000]; 4 – Приморский край у г. Фокино, по: ПроЗорова, Фоменко [2015]; 5, 6 – Курильские острова, Шикотан и Зеленый, по: ПроЗорова [2000, 2002]; 7 – г. Петропавловск-Камчатский.

Fig. 2 in Distribution of an invasive slug, Arion subfuscus (Draparnaud, 1805) in East Asia from Kamchatka to China

Fig. 2. Arion subfuscus from Kamchatka, Petropavlovsk-Kamchatsky City. Photo by O.A. Chernyagina (yellow-orange bodmucus produced by slugs is visible).

Fig. 4 in Distribution of an invasive slug, Arion subfuscus (Draparnaud, 1805) in East Asia from Kamchatka to China

Fig. 4. Location of Arion subfuscus in Petropavlovsk-Kamchatsky City near Kultuchnoye Lake. Photo by O.A. Chernyagina.

Рис. 2. Arion subfuscus c Камчатки, г. Петропавловск-Камчатский. Фото О.А. ЧернЯгиной (Заметно выделение желтооранжевой слиЗи). in Distribution of an invasive slug, Arion subfuscus (Draparnaud, 1805) in East Asia from Kamchatka to China

Рис. 2. Arion subfuscus c Камчатки, г. Петропавловск-Камчатский. Фото О.А. ЧернЯгиной (Заметно выделение желтооранжевой слиЗи).

Fig. 3 in Distribution of an invasive slug, Arion subfuscus (Draparnaud, 1805) in East Asia from Kamchatka to China

Fig. 3. Findings of Arion subfuscus in East Asia: 1–3 – China, after Wiktor et al. [2000]; 4 – Primorsky Krai near Fokino Town, after Prozorova, Fomenko [2015]; 5, 6 – Kuril Islands, Shikotan and Zelyony isls., after Prozorova [2000, 2002]; 7 – Petropavlovsk-Kamchatsky City.

FIG. 5 in Phylogénie moléculaire et données paléobiogéographiques sur le gastéropode terrestre Tudorella sulcata (Draparnaud, 1805) en France et en Algérie orientale

FIG. 5. — Tudorella sulculata (Draparnaud,1805), Pliocène supérieur, Puimoisson, France (collection F. Magnin). Échelle: 5 mm.

FIG. 2 in Phylogénie moléculaire et données paléobiogéographiques sur le gastéropode terrestre Tudorella sulcata (Draparnaud, 1805) en France et en Algérie orientale

FIG. 2. – Présence de Tudorella sulcata (Draparnaud, 1805) s.l. en France et en Algérie. Les divisions administratives (départements ou wilayas) dans lesquelles l'espèce est présente sont représentés en gris. Les localités de l'extrême ouest algérien se rapportent à T. mauritanica (Pallary, 1898) et ne sont pas étudiées ici. Échelles: 200 km.

FIG. 1 in Phylogénie moléculaire et données paléobiogéographiques sur le gastéropode terrestre Tudorella sulcata (Draparnaud, 1805) en France et en Algérie orientale

FIG. 1. — Tudorella sulcata (Draparnaud, 1805) s.l.: A, individu vivant en activité (Marseille, France), 17,5 mm; B-D, coquilles après dissection; B, Bejaïa, Algérie, 18 mm; C, El Khroub, Algérie, 17,5 mm; D, Annaba, Algérie, 16,5 mm.

FIG. 4 in Phylogénie moléculaire et données paléobiogéographiques sur le gastéropode terrestre Tudorella sulcata (Draparnaud, 1805) en France et en Algérie orientale

FIG. 4. — Tudorella draparnaudi (Beck 1837), Miocène moyen, Mirabeau, France (collection F. Magnin). Échelles: 5 mm.

FIG. 3 in Phylogénie moléculaire et données paléobiogéographiques sur le gastéropode terrestre Tudorella sulcata (Draparnaud, 1805) en France et en Algérie orientale

FIG. 3. — Phylogrammes: arbres de consensus majoritaire (50 %) des arbres échantillonnés par l'analyse bayésienne. À gauche (ADNmt), séquençage de la COI basé sur 689 paires de bases (bp). À droite (ADNn), séquençage de l'ITS-1 basé sur 367 paires de base. Les chiffres en gras représentent les probabilités postérieures bayésiennes des noeuds. Abréviations: BON, plaine de Bonnieu, Martigues, France; CAB, Cabo de los Caballeros, Minorque, Espagne; CEN, Rass el Hamra « Centaurées », Annaba (ex-Bône), Algérie; GBH, gorges de Ben Haroun, Jijel/Mila, Algérie; HAM, Rass el Hamra « Argiles », Annaba (ex-Bône), Algérie; KHR, El Khroub, Constantine, Algérie; RES, pointe de Resquiadou, Le Rove, France; ROU, Roucas-Blanc, Marseille, France; SES, Rass el Hamra « Sésélis », Annaba (ex-Bône), Algérie; SUG, Sugiton, Marseille, France; YEM, Yemma Gouraya, Béjaïa, Algérie.

Fig. 1 in The architecture of the physid musculature of Physa acuta Draparnaud, 1805 (Gastropoda: Physidae)

Fig. 1. (A) Dorsal view of P. acuta with all visceral structures removed to show the broad insertion of the physid muscle s.s. (Pm) in the columellar muscle (Cm) in the snail foot. The Cm has two pedal horns that run anteriorly towards the head while the thicker posterior part runs a short distance towards the tail. The anterior horns start as thick bundles but taper as they near the head. (B) Dorsal view of P. acuta with its visceral hump removed to show the Pm and its five branches numbered Pm1–5. Pm1 runs anteriorly from the origin to the neck and head, Pm2 across the neck to the left hand side of the head, Pm3 and Pm4 descend to the left side of the body and Pm5 wraps around the Cm before passing anteriorly, also to the left hand side of the body. The columellar muscle was not drawn but is located inside the loop made by Pm5. (C) Dorsolateral view of P. acuta with the skin and visceral hump removed. The branches of the Pm are seen coming from right to left over the anterior part of body, intertwining as they do so with Cm fibres that run from the middle to the anterior part of the body. Pm fibres are overlain by Cm fibres. (D) Lateral view of P. acuta showing the location of Pm branches 2–5 within the snail body where they overlie each other. Pm1 is obscured. The fan muscle (Pf) radiates posteriorly from its origin on the physid muscle s.s. (Pm) to a diffuse insertion beneath the mantle.

Fig. 4 in The architecture of the physid musculature of Physa acuta Draparnaud, 1805 (Gastropoda: Physidae)

Fig. 4. (A) Lateral view of P. acuta showing the columellar muscle (Cm) and its relationship with the female and male pores. Also shown are Cm branches running towards the head and side, the insertion of Cm into the foot and the posterior part of the Cm that attaches to the shell. (B) Lateral view of P. acuta showing the relationship between the Pm (dotted line), the Cm, fan muscle (Pf) and the pneumostome–mantle band" of fibres (Pp) on the roof of the mantle. (C) Dorsal view of P. acuta (visceral hump removed) showing the relationship between the branches Pm2–Pm5 of the physid muscle s.s. associated with the 'cervical septum' (dotted lines) and the columellar muscle (Cm).

Fig. 2 in The architecture of the physid musculature of Physa acuta Draparnaud, 1805 (Gastropoda: Physidae)

Fig. 2. (A) Dorsal view of P. acuta showing the muscles overlying the lung floor, viz. thin bands of fibres (Plu) from the main trunk of the physid muscle s.s. (Pm) and from the columellar muscle (Cm). The anterior corner of the pneumostome is indicated in the lower mid-portion of the visceral hump but is not drawn. (B) Lateral view of P. acuta showing the pneumostome–mantle band of muscle fibres (Pp). This band runs from the left anterior part of the mantle roof (i.e. the anterior corner of the pneumostome) towards the right hand side of the roof, anchoring on the fan muscle (see also Fig. 2C). (C) Floor of the mantle cavity after removal of the lung tissue, showing in its mid-portion the pneumostome–mantle band of muscle fibres (Pp) that seems to give support to the opening of the pneumostome. The uppermost of these fibres converge at the edge of the mantle collar and immediately below are those (removed) that support the kidney.

Fig. 3 in The architecture of the physid musculature of Physa acuta Draparnaud, 1805 (Gastropoda: Physidae)

Fig. 3. (A) Transverse view of the body at the level of the lung floor as seen from below showing the physid muscle s.s. (Pm) and columellar muscle (Cm). Fibres from the Pm (Plu) and columellar muscle (Cm) cross the lung floor (fine detail indicated in upper right hand corner of the lung floor). The lung floor is surrounded by mantle collar tissue. (B) Dorsal view of P. acuta with the visceral hump removed to show the dorsal components of the columellar muscle (Cm). These have been flattened slightly. No detail is shown on the lung floor. (C) Above – dissection of the columellar muscle (Cm) and its four elements (slightly flattened). Below – detail of Cm overlying Pm4 and Pm5 fibres as they pass into the foot.

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Figs 1–4 in A new species of the genus Cymindis Latreille, 1805 (Coleoptera: Carabidae: Lebiini) from the Kunlun Mt. Range, China

Figs 1–4. Cymindis (Iscariotes) kalabi sp. n. 1 – holotype, male, habitus, dorsal view; 2 –

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Figs 1–3 in A new species of the genus Cymindis Latreille, 1805 (Coleoptera: Carabidae: Lebiini) from the Tarim River basin, China

Figs 1–3. Cymindis (Tarsostinus) rolandi sp. n., female. 1 – holotype, habitus, dorsal

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Fig. 2 in Association of the louse-flies of the genus Ornothoctona Speiser, 1902 (Diptera: Hippoboscidae) with birds and first record of O. australasiae (Fabricius, 1805) from the Russian Far East

Fig. 2. Records of Ornithoctona australasiae (Fabricius, 1805) in the Palearctic region.

Fig. 1 in Distribution of an invasive slug, Arion subfuscus (Draparnaud, 1805) in East Asia from Kamchatka to China

Fig. 1. Arion subfuscus from Primorsky Krai near Fokino Town. Photo by L.A. Prozorova.

Рис. 1. Arion subfuscus иЗ Приморского краЯ вблиЗи г. Фокино. Фото Л.А. ПроЗоровой. in Distribution of an invasive slug, Arion subfuscus (Draparnaud, 1805) in East Asia from Kamchatka to China

Рис. 1. Arion subfuscus иЗ Приморского краЯ вблиЗи г. Фокино. Фото Л.А. ПроЗоровой.