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Figure 6 in A third European species of grayling (Actinopterygii, Salmonidae), endemic to the Loire River basin (France), Thymallus ligericus n. sp.

Figure 6. – Dorsal fin on a live paratype of Thymallus ligericus n. sp. MNHN 2018-0726, 290 mm SL ♀, Lignon River at Boën-surLignon, 29 May 2015, Persat, Juglaret and Buttazzoni coll.

Figure 4 in A third European species of grayling (Actinopterygii, Salmonidae), endemic to the Loire River basin (France), Thymallus ligericus n. sp.

Figure 4. – Mouth in ventral view of Thymallus spp. A: Holotype of Thymallus ligericus n. sp. MNHN 2018-0722, 337 mm SL J, Alagnon River at La Chapelle d'Alagnon, 9 Sep. 2016, Persat and FDAAPPMA15 coll.; B: Thymallus thymallus UCBLZ 2012.9.1010, 376 mm TL, Rhône drainage, Ain River at Crotenay, 10 Jun. 2014, Persat and FDAAPPMA39 coll.

Figure 2 in A third European species of grayling (Actinopterygii, Salmonidae), endemic to the Loire River basin (France), Thymallus ligericus n. sp.

Figure 2. – Specimens of Thymallus spp. in lateral view. Holotype of Thymallus ligericus n. sp. MNHN 2018- 0722, 337 mm SL J, Alagnon River at La Chapelle d'Alagnon, 9 Sep. 2016, Persat and FDAAPPMA 15 coll., in live (A) and after preservation (B); Paratype of Thymallus ligericus n. sp. MNHN 2019-0267 (C), 269 mm SL ♀, Loire River at Chadron, 22 Sep. 2016, Persat and ONEMA43 coll; UCBLZ – 2012.9.1011 (D), 292 mm TL, Rhône drainage, Ain River at Crotenay, 10 Jun. 2014, Persat and FDAAPPMA39 coll.

Figure 1 in A third European species of grayling (Actinopterygii, Salmonidae), endemic to the Loire River basin (France), Thymallus ligericus n. sp.

Figure 1. – The three supplementary measurements made on the ventral side of the head, in addition to those of Surre et al. (1986): the mandible width, the chin length (from the basibranchial junction to the extremity of the mandible) and the ventral snout length (from the same point to the extremity of the snout).

Figure 3 in A third European species of grayling (Actinopterygii, Salmonidae), endemic to the Loire River basin (France), Thymallus ligericus n. sp.

Figure 3. – Head profiles of Thymallus spp. A: Paratype of Thymallus ligericus n. sp. MNHN 2018-0728, 300 mm SL J, Dore River at Vertolaye, 29 May 2015, Persat, Juglaret and Buttazzoni coll.; B: Thymallus thymallus UCBLZ – 2012.9.1010, 376 mm TL, Rhône drainage, Ain River at Crotenay, 10 Jun. 2014, Persat and FDAAPPMA39 coll.

Figure 5 in Barbatula leoparda (Actinopterygii, Nemacheilidae), a new endemic species of stone loach of French Catalonia

Figure 5. – Distribution map of the three recognized Barbatula spp. in France and Spain adapted and modified from Kottelat and Freyhof (2007): Barbatula leoparda in yellow, Barbatula barbatula in blue and Barbatula quignardi in orange. Locations: Têt River at Nefiach (1), Tech River at Céret (2) and at Elne (3).

Figure 2 in Barbatula leoparda (Actinopterygii, Nemacheilidae), a new endemic species of stone loach of French Catalonia

Figure 2. – Specimens of Barbatula spp. in ventral view. A: Holotype of Barbatula leoparda MNHN 2018- 0228, 62.6 mm SL ♀, Têt River at Nefiach, 7 Sep. 2016, Denys and ONEMA coll.; B: Barbatula barbatula MNHN 2013-0826, 72.9 mm SL ♂, stream Clauge (Rhône drainage) at La Loye, 1 Jul. 2013, Denys and ONEMA coll.; C: Holotype of Barbatula quignardi MGAB77, 52 mm SL ♂, Lez River, Jul. 1962, Băcescu coll.

Fig. 2 in A new colorful species of Geophagus (Teleostei: Cichlidae), endemic to the rio Aripuanã in the Amazon basin of Brazil

Fig. 2. Geophagus mirabilis, paratype, NUP 15117, 107.8 mm SL, Brazil, State of Mato Grosso, município de Juína, rio Aripuanã, upstream from Dardanelos/Andorinhas falls, immediately after capture. Photograph by Cláudio H. Zawadzki.

Fig. 5 in A new colorful species of Geophagus (Teleostei: Cichlidae), endemic to the rio Aripuanã in the Amazon basin of Brazil

Fig. 5. Geophagus mirabilis, living specimen in aquarium, not preserved. Photograph by Oliver Lucanus.

Fig. 6 in A new colorful species of Geophagus (Teleostei: Cichlidae), endemic to the rio Aripuanã in the Amazon basin of Brazil

Fig. 6. Map of the geographic distribution of Geophagus mirabilis. Star corresponds to type-locality; circles correspond to other localities where the species is found. One symbol can correspond to more than one locality.

Fig. 1 in A new colorful species of Geophagus (Teleostei: Cichlidae), endemic to the rio Aripuanã in the Amazon basin of Brazil

Fig. 1. Geophagus mirabilis, holotype, MCP 48123, 124.1 mm SL, Brazil, State of Mato Grosso, município de Aripuanã, rio Aripuanã upstream from Dardanelos falls. Photograph by Luiz F. C. Tencatt.

Fig. 4. Geophagus mirabilis, NUP 15117, 107.8 in A new colorful species of Geophagus (Teleostei: Cichlidae), endemic to the rio Aripuanã in the Amazon basin of Brazil

Fig. 4. Geophagus mirabilis, NUP 15117, 107.8 mm SL, Brazil, State of Mato Grosso, município de Juína, rio Aripuanã, upstream from Dardanelos/Andorinhas falls. Lower pharyngeal jaw in occlusal aspect, anterior portion upwards. (A) and (B), lateral view of two different teeth, proportionally enlarged, anterior portion to left side. Scale bar = 1 mm, not applied to (A) and (B).

Fig. 3 in A new colorful species of Geophagus (Teleostei: Cichlidae), endemic to the rio Aripuanã in the Amazon basin of Brazil

Fig. 3. Ventral view of head, showing the shape of lips, in (A) Geophagus mirabilis, paratype, UFRO-I 21285, 151.6 mm SL, Brazil, State of Mato Grosso, município de Aripuanã, rio Aripuanã, upstream from Dardanelos/Andorinhas falls; (B) G. camopiensis, MZUSP 32888, 112.6 mm SL. Arrow heads indicate lateralis foramina 1 and 2 in (A) and lateralis foramen 2 in (B). Photograph by Celso Ikedo.

Fig. 2 in Diet and ecomorphological relationships of an endemic, species-poor fish assemblage in a stream in the Iguaçu National Park

Fig. 2. Ordenation of the fish fauna in Jumelo stream, Iguaçu National Park, Paraná, Brazil, produced by the first two axes of the principal components analysis (PCA 1 and PCA 2) applied to the correlation of 15 ecomorphological indices and the mouth orientations of the fish species.

Fig. 1 in Diet and ecomorphological relationships of an endemic, species-poor fish assemblage in a stream in the Iguaçu National Park

Fig. 1. Study area. Collection point in stream Jumelo, region of the Iguaçu National Park in the Brazilian state of Paraná and Gonçalves Dias River in the Iguaçu River Basin, Santa Tereza do Oeste, Paraná.

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Figure 3 in Avifauna of the Adelbert Mountains, New Guinea: why is Fire-maned Bowerbird Sericulus bakeri the mountains' only endemic bird species?

Figure 3. Terrain map of north-east New Guinea. Areas above 500 m are coloured grey; areas between 300 and 500 m blue; and areas below 300 m green. 1 = the Gogol River valley, between the Adelbert Mts. to the north and the Finisterre Mts. of the Huon Peninsula to the south. 2 = the Ramu River valley, between the Adelberts to the north-east and the Central Range to the south-west. 3 = the upper Ramu River valley and its headwaters, between the Finisterre Mts. of the Huon Peninsula to the north and the Central Range to the south. 4 = the Sepik River basin, between the Adelbert Mts. to the east and Prince Alexander Mts. of the North Coastal Range to the west. Map kindly produced by Iain Woxvold.

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Figure 2 in Avifauna of the Adelbert Mountains, New Guinea: why is Fire-maned Bowerbird Sericulus bakeri the mountains' only endemic bird species?

Figure 2. Presence and absence of Sericulus bowerbirdsȱonȱNewȱGuinea'sȱnorthernȱwatershed,ȱmodifiedȱfromȱ Diamondȱ(1969).ȱEachȱfilledȱdotȱrepresentsȱrecordsȱbyȱoneȱobserver.ȱThereȱareȱonlyȱsevenȱdocumentedȱareasȱ of occurrence of the allospecies Masked Bowerbird S. aureus, numbered from west to east, with observer names in parentheses: 1 = Tamrau Mts. (E. T. Gilliard and B. M. Beehler) and Arfak Mts. (many observers) of the Vogelkop. 2 = Wandammen Mts. (E. Mayr). 3 = Weyland Mts. (F. Shaw-Mayer). 4 = Bernhard Camp (A. Rand). 5 = Foja Mts. (B. M. Beehler and J. Diamond). 6 = Mt. Nibo (J. Diamond). 7 = Mt. Turu (J. Diamond). The asterisk depicts the range of the allospecies Fire-maned Bowerbird S. bakeri in the Adelberts. X = areas surveyedȱintensivelyȱwithoutȱfindingȱanyȱSericulus.? = an undocumented report of S. aureus from the Jimi River.ȱExceptȱforȱtheȱlatter,ȱS. aureus is known mainly from outlying ranges (locations 1, 2, 5, 6 and 7). There are only two documented localities for it in the Central Range (3–4), and there is a large gap between the easternmost record of S. aureus (7) and the range of S. bakeri. The remaining Sericulus allospecies in New Guinea is Flame Bowerbird S. ardens of the southern watershed.

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Figure 1 in Avifauna of the Adelbert Mountains, New Guinea: why is Fire-maned Bowerbird Sericulus bakeri the mountains' only endemic bird species?

Figure 1. New Guinea's principal mountain ranges: the Central Range forming New Guinea's backbone; and the ten outlying ranges along the north and north-west coasts, from Huon and Adelbert in the east, to Fakfak and Kumawa in the west.

Figs. 34-39. 34, 35 in Review of the genus Malaxella (Hemiptera: Fulgoroidea: Delphacidae) endemic in China, with a description of a new species

Figs. 34-39. 34, 35. Malaxella flava Ding & Hu. Female; 36, 37: Malaxella macracantha Ren & Qin sp. nov. Male; 38, 39: Malaxella tetracantha Qin & Zhang. Female. 34, 36, 38. Head and thorax, dorsal view; 35, 37, 39. Frons and clypeus. Scale bars = 0.20 mm.

Figs. 28-33. 28, 29 in Review of the genus Malaxella (Hemiptera: Fulgoroidea: Delphacidae) endemic in China, with a description of a new species

Figs. 28-33. 28, 29. Malaxella flava Ding & Hu. Female; 30, 31: Malaxella macracantha Ren & Qin sp. nov. Male; 32, 33: Malaxella tetracantha Qin & Zhang. Female. 28, 30, 32. Habitus, dorsal view; 29, 31, 33. Habitus, lef lateral view. Scale bars = 0.50 mm.