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Fig. 1 in Short Communication A new record of the rare Hypleurochilus bananensis (Poll 1959) (Actinopterygii: Blenniidae) with a review of its distribution and ecology in Italian seas

Fig. 1 - Known distribution of Hypleurochilus bananensis in Italian waters updated to January 2024 (records of this study are included). Black circles indicate areas where the species was recorded. For details see Table 1. / Distribuzione nota di Hypleurochilus bananensis nelle acque italiane aggiornata al gennaio 2024 (sono incluse le registrazioni di questo studio). I cerchi neri indicano le aree in cui la specie è stata registrata. Per i dettagli si veda la Tabella 1.

Fig. 5 in Biology of the blind geobiont scarab beetle genus Chaetonyx Schaum, 1862 (Scarabaeidae: Orphninae) with new distribution records of Ch. robustus Schaum, 1862 from Bulgaria

Fig. 5. Life cycle of Chaetonyx robustus. Diagram is constructed based on the investigation of the local population in riverside habitat at the Zemen Gorge, SW Bulgaria, in April 2012 to November 2014.

Fig. 4 in Biology of the blind geobiont scarab beetle genus Chaetonyx Schaum, 1862 (Scarabaeidae: Orphninae) with new distribution records of Ch. robustus Schaum, 1862 from Bulgaria

Fig. 4. Different stages of Chaetonyx robustus. A, B: Eggs and first instar larvae (laboratory rearing, eggs collected on 03–VIII–2014); C: Pupae, collected on 07–VII–2013 (in vivo imaging); D: Adult, pupa, larvae from the three instars and eggs (in vivo imaging, material was collected on 07–VII–2013). Scale bars: A: 1 mm; B: 0.5 mm; C, D: 2.5 mm.

Fig. 3 in Biology of the blind geobiont scarab beetle genus Chaetonyx Schaum, 1862 (Scarabaeidae: Orphninae) with new distribution records of Ch. robustus Schaum, 1862 from Bulgaria

Fig. 3. Adults of Chaetonyx robustus, excavated from the site near town of Zemen (in situ imaging). A: sampling on 04–VIII–2012; B: sampling on 02–IX–2012.

Fig. 2 in Biology of the blind geobiont scarab beetle genus Chaetonyx Schaum, 1862 (Scarabaeidae: Orphninae) with new distribution records of Ch. robustus Schaum, 1862 from Bulgaria

Fig. 2. Adults of Chaetonyx robustus with different degrees of sclerotization, collected on 04– VIII–2012 from the sampling site. A: Slightly sclerotized, just emerged from the pupae; B: Moderate sclerotization; C: Fully sclerotized, adult from previous generation. Scale bar: 2.5 mm.

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Рис. 4. Карта-схема мест встреч пятнистого оΛеня в Нижнем Приамурье в 1979–2021 гг. КваΑраты — места фоторегистрации: 1 — верховья рр. Обор и Àурмин; 2, 3 — Анюйский национаΛьный парк; круги — места встреч по Λитературным и опросным Αанным: 1 — окрестности с. Кутузовка (место первой регистрации в 1979 г.); 2 — верховья р. СиΑима; 3 — устье р. Нижняя Буге; 4 — бассейн р. Мухен; 5–8 — Анюйский национаΛьный парк (соответственно, р. Пихца, урочище Сира, окрестности с. Арсеньево, устье р. СоΛоми); 9 — среΑнее течение р. СоΛоми; 10 — 76 км трассы ΔиΑога — Ванино; 11 — бассейн р. Кия; 12 — бассейн р. ХойΑур; 13 — бассейн р. Нюра Fig. 4. A schematic map of sika deer sightings in the Lower Amur Region in 1979-2021. Squares designate sites of photo recording: 1 — upper reaches of the rivers Obor and Durmin; 2, 3 — Anyui National Park; circles designate sightings sites according to the literature and the survey data: 1 — vicinity of the village Kutuzovka (the place of the first registration in 1979); 2 — upper reaches of the river Sidima; 3 — the mouth of the river Lower Buge; 4 — the Mukhen River basin; 5-8 —Anyui National Park (respectively, the Pikhtsa River, the Sira tract, the vicinity of the village Arsenyevo, the mouth of the Solomi River); 9 — the middle course of the Solomi River; 10 — 76 km of the Lidoga-Vanino Highway; 11 — the Kiya River basin; 12 — the Khoydur River basin; 13 — the Nyura River basin in New data on the distribution of sika deer Cervus nippon Temminck, 1838 in the Lower Amur Region

Рис. 4. Карта-схема мест встреч пятнистого оΛеня в Нижнем Приамурье в 1979–2021 гг. КваΑраты — места фоторегистрации: 1 — верховья рр. Обор и Àурмин; 2, 3 — Анюйский национаΛьный парк; круги — места встреч по Λитературным и опросным Αанным: 1 — окрестности с. Кутузовка (место первой регистрации в 1979 г.); 2 — верховья р. СиΑима; 3 — устье р. Нижняя Буге; 4 — бассейн р. Мухен; 5–8 — Анюйский национаΛьный парк (соответственно, р. Пихца, урочище Сира, окрестности с. Арсеньево, устье р. СоΛоми); 9 — среΑнее течение р. СоΛоми; 10 — 76 км трассы ΔиΑога — Ванино; 11 — бассейн р. Кия; 12 — бассейн р. ХойΑур; 13 — бассейн р. Нюра Fig. 4. A schematic map of sika deer sightings in the Lower Amur Region in 1979-2021. Squares designate sites of photo recording: 1 — upper reaches of the rivers Obor and Durmin; 2, 3 — Anyui National Park; circles designate sightings sites according to the literature and the survey data: 1 — vicinity of the village Kutuzovka (the place of the first registration in 1979); 2 — upper reaches of the river Sidima; 3 — the mouth of the river Lower Buge; 4 — the Mukhen River basin; 5-8 —Anyui National Park (respectively, the Pikhtsa River, the Sira tract, the vicinity of the village Arsenyevo, the mouth of the Solomi River); 9 — the middle course of the Solomi River; 10 — 76 km of the Lidoga-Vanino Highway; 11 — the Kiya River basin; 12 — the Khoydur River basin; 13 — the Nyura River basin

Fig. 16 in Figs. 18-21 in Using the Integrative Approach to Update a Gap of One Century: Redescription and New Distribution Records of the South American Tarantulas (Araneae: Mygalomorphae: Theraphosidae).

Fig. 16. Mothocya parvostis manca (2.96 mm) infesting a yellowfin seabream Acanthopagrus latus juvenile (12.22 mm). (A–D) Pereopods 3–6, respectively. (E, F) Pleopods 1, 2, respectively. Scale bars = 0.1 mm.

Fig. 14 in Figs. 18-21 in Using the Integrative Approach to Update a Gap of One Century: Redescription and New Distribution Records of the South American Tarantulas (Araneae: Mygalomorphae: Theraphosidae).

Fig. 14. Mothocya parvostis manca (3.12 mm) infesting a cobaltcap silverside Hypoatherina tsurugae juvenile (14.54 mm). (A–D) Pereopods 3–6, respectively. (E, F) Pleopods 1, 2, respectively. Scale bars = 0.1 mm.

Fig. 15 in Figs. 18-21 in Using the Integrative Approach to Update a Gap of One Century: Redescription and New Distribution Records of the South American Tarantulas (Araneae: Mygalomorphae: Theraphosidae).

Fig. 15. Mothocya parvostis manca (2.96 mm) infesting a yellowfin seabream Acanthopagrus latus juvenile (12.22 mm). (A) Body, dorsal view. (B) Cephalon, ventral view. (C) Pleotelson. (D, E) Pereopods 1, 2, respectively. Scale bars: A = 1 mm; B, C = 0.2 mm; D, E = 0.1 mm.

Fig. 12 in Figs. 18-21 in Using the Integrative Approach to Update a Gap of One Century: Redescription and New Distribution Records of the South American Tarantulas (Araneae: Mygalomorphae: Theraphosidae).

Fig. 12. Mothocya parvostis juvenile (6.89 mm) infesting a yellowfin seabream Acanthopagrus latus juvenile (23.27 mm). (A–E) Pereopods 3–7, respectively. (F, G) Pleopods 1, 2, respectively. Scale bars = 0.2 mm.

Fig. 11 in Figs. 18-21 in Using the Integrative Approach to Update a Gap of One Century: Redescription and New Distribution Records of the South American Tarantulas (Araneae: Mygalomorphae: Theraphosidae).

Fig. 11. Mothocya parvostis juvenile (6.89 mm) infesting a yellowfin seabream Acanthopagrus latus juvenile (23.27 mm). (A) Body, dorsal view. (B) Cephalon, ventral view. (C) Pleotelson. (D, E) Pereopods 1, 2, respectively. Scale bars: A–C = 1 mm; D, E = 0.2 mm.

Fig. 10 in Figs. 18-21 in Using the Integrative Approach to Update a Gap of One Century: Redescription and New Distribution Records of the South American Tarantulas (Araneae: Mygalomorphae: Theraphosidae).

Fig. 10. Mothocya parvostis juvenile (7.19 mm) infesting a cobaltcap silverside Hypoatherina tsurugae juvenile (50.84 mm). (A–E) Pereopods 3–7, respectively. (F, G) Pleopods 1, 2, respectively. Scale bars = 0.2 mm.

Fig. 9 in Figs. 18-21 in Using the Integrative Approach to Update a Gap of One Century: Redescription and New Distribution Records of the South American Tarantulas (Araneae: Mygalomorphae: Theraphosidae).

Fig. 9. Mothocya parvostis juvenile (7.19 mm) infesting a cobaltcap silverside Hypoatherina tsurugae juvenile (50.84 mm). (A) Body, dorsal view. (B) Cephalon, ventral view. (C) Pleotelson. (D, E) Pereopods 1, 2, respectively. Scale bars: A–C = 1 mm; D, E = 0.2 mm.

Fig. 7 in Figs. 18-21 in Using the Integrative Approach to Update a Gap of One Century: Redescription and New Distribution Records of the South American Tarantulas (Araneae: Mygalomorphae: Theraphosidae).

Fig. 7. Prevalence of the standard-length range of juveniles of cobaltcap silverside Hypoatherina tsurugae and yellowfin seabream Acanthopagrus latus. Diagonal shading bars (red), dot bars (blue), grid bars (green), and plain bars (light blue) indicate the manca-prevalence, juvenile-prevalence, the percentage of fish parasitised by both mancae and juveniles, and non-infested fishes, respectively. The asterisk indicates no data.

Fig. 13 in Figs. 18-21 in Using the Integrative Approach to Update a Gap of One Century: Redescription and New Distribution Records of the South American Tarantulas (Araneae: Mygalomorphae: Theraphosidae).

Fig. 13. Mothocya parvostis manca (3.12 mm) infesting a cobaltcap silverside Hypoatherina tsurugae juvenile (14.54 mm). (A) Body, dorsal view. (B) Cephalon, ventral view. (C) Pleotelson. (D, E) Pereopods 1, 2, respectively. Scale bars: A = 1 mm; B, C = 0.2 mm; D, E = 0.1 mm.

Fig. 8 in Figs. 18-21 in Using the Integrative Approach to Update a Gap of One Century: Redescription and New Distribution Records of the South American Tarantulas (Araneae: Mygalomorphae: Theraphosidae).

Fig. 8. Neighbor-joining trees showing seven and eight haplotypes of the cytochrome c oxidase subunit I (COI) and 16S rRNA gene infesting juveniles of cobaltcap silverside Hypoatherina tsurugae and yellowfin seabream Acanthopagrus latus along with selected sequences of other cymothoids downloaded from GenBank. Bootstrap values less than 98% are not shown. The accession numbers were deposited in GenBank (under registration).

Fig. 6 in Figs. 18-21 in Using the Integrative Approach to Update a Gap of One Century: Redescription and New Distribution Records of the South American Tarantulas (Araneae: Mygalomorphae: Theraphosidae).

Fig. 6. Prevalence, manca-prevalence, and juvenile-prevalence for each sampling day in juveniles of cobaltcap silverside Hypoatherina tsurugae and yellowfin seabream Acanthopagrus latus. Closed circles (green), closed triangles (blue), and closed squares (red) indicate the prevalence, the mancaprevalence, and the juvenile-prevalence, respectively.

Fig. 4 in Figs. 18-21 in Using the Integrative Approach to Update a Gap of One Century: Redescription and New Distribution Records of the South American Tarantulas (Araneae: Mygalomorphae: Theraphosidae).

Fig. 4. Scatter plots of the standard length of non-infested and infested fish for each sampling date in juveniles of cobaltcap silverside Hypoatherina tsurugae and yellowfin seabream Acanthopagrus latus. The open circles (black) indicate non-infested fish, and the closed triangles (red) indicate infested fish. The solid lines (black) for non-infested fishes and the broken lines (red) for infested fishes are regression lines.

Fig. 3 in Figs. 18-21 in Using the Integrative Approach to Update a Gap of One Century: Redescription and New Distribution Records of the South American Tarantulas (Araneae: Mygalomorphae: Theraphosidae).

Fig. 3. Dorsal and ventral views of Mothocya parvostis infesting juveniles of cobaltcap silverside Hypoatherina tsurugae (A and B) and yellowfin seabream Acanthopagrus latus (C and D). A and C: mancae, B and D: M. parvostis juveniles. Scale bars = 1 mm.

Fig. 5 in Figs. 18-21 in Using the Integrative Approach to Update a Gap of One Century: Redescription and New Distribution Records of the South American Tarantulas (Araneae: Mygalomorphae: Theraphosidae).

Fig. 5. Scatter plots of the standard length of fishes and the total length of M. parvostis in juveniles of cobaltcap silverside Hypoatherina tsurugae and yellowfin seabream Acanthopagrus latus. The solid lines are regression lines.