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Figure 2 in A new species of the Liolaemus nigroviridis group from the Andes of Central Chile (Iguania: Liolaemidae)

Figure 2. Principal Component Analysis (PCA) plots of the species of the L. nigroviridis group, performed with the residuals of each character regressed on snout-vent length. On the left panels, the individuals are colored according to their species as shown on the legend on the top right corner. Ellipses represent the 95% confidence interval around the centroid for each species. On each axis, the PC is labeled according to its number and the percentage of the total variance that PC explains. On the right, the variable graphs, which illustrate the contribution of each variable to the construction of the axes.

Figure 5 in A new species of the Liolaemus nigroviridis group from the Andes of Central Chile (Iguania: Liolaemidae)

Figure 5. Species of the Liolaemus nigroviridis group. A) Male of L. campanae (photograph by S. Berhó Fuenzalida). B) Female of L. campanae (photograph by R. Arroyo Castro). C) and D) Males of L. fuscus (photographs by JTP). E) and F) Males of L. nigroviridis (photographs by JTP). G) Female of L. nigroviridis (photograph by JTP). H) and I) Male and female, respectively, of of L. uniformis (photographs by JTP).

Figure 4 in A new species of the Liolaemus nigroviridis group from the Andes of Central Chile (Iguania: Liolaemidae)

Figure 4. Liolaemus nigrodorsum sp. nov. A) and B) Holotype, male SSUC Re 787. C) and D) Paratype, female SSUC Re 792. E) SSUC Re 789 and F) SSUC Re 788, paratypes, males.

Figure 1 in A new species of the Liolaemus nigroviridis group from the Andes of Central Chile (Iguania: Liolaemidae)

Figure 1. Phylogenetic relationships of the species of the L. nigroviridis complex group, modified from Torres-Pérez et al. (2017), based on the mitochondrial gene cytochrome b, including the bootstrap values for maximum likelihood, the posterior probabilities for Bayesian inference and the number of haplotypes used for each terminal taxon. Liolaemus fuscus is added as the basal species of the group, following Schulte and Moreno-Roark (2010), Troncoso-Palacios et al. (2015) and Esquerré et al. (2022). Specific name L. nigroviridis is used only for the clade that contains the samples from near the type locality. The candidate species Liolaemus sp. Arpa is in red. Male dorsal pattern is compared.

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Figure 3 in Description of Upeneus madras (Mullidae), a new goatfish species from SE India (NE Indian Ocean), with establishment of the pori-species group and a review of barbel colour in Upeneus species

Figure 3. – Relationship among five morphometric characters in Upeneus madras n. sp. and four other species of the pori group.

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Figure 4 in Description of Upeneus madras (Mullidae), a new goatfish species from SE India (NE Indian Ocean), with establishment of the pori-species group and a review of barbel colour in Upeneus species

Figure 4. – Relationship among four morphometric characters in Upeneus madras n. sp. and U. guttatus from the NE Indian Ocean (NEIO) and all other areas of the Indo-Pacific, showing data for the newly designated lectotype (LT) and paralectotype (PLT).

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Figure 1. – A-I in Description of Upeneus madras (Mullidae), a new goatfish species from SE India (NE Indian Ocean), with establishment of the pori-species group and a review of barbel colour in Upeneus species

Figure 1. – A-I: The nine species of the pori group: A: Upeneus madras n. sp., BPBM 20658, PT, 110 mm SL, Chennai, SE India (J.E. Randall); B: U. asymmetricus, CSIRO H 7517-02, 93 mm SL, Lombok, S Indonesia (W.T. White); C: U. australiae, CSIRO H 4056-01, 105 mm SL (A. Graham); D: U. dimipavlov, VNMN-I 2056, HT, 120 mm SL, N of Hon Tre Island, Nha Trang, S-central Vietnam (D.A. Pavlov); E: Upeneus elongatus, KAUM-I. 58746, HT, 89 mm SL, Tanega-shima Island, S Japan (H. Motomura); F: U. floros, SAIAB 204583, HT, 107 mm SL, Two Miles Reef, Sodwana Bay, KwaZulu-Natal, South Africa (C. Floros); G: U. itoui KAUM-I. 13595, PT, 118 mm SL, Kagoshima Prefecture, S Japan (H. Motomura); H: U. pori, SAIAB 209540 (wrongly referred to as SAIAB 192775 by Uiblein et al., 2020: fig. 6F, and Uiblein and Motomura, 2021: fig. 7E), 94 mm SL, off NE Madagascar (J. Escobar-Porras); I: U. willwhite, CSIRO H 7217-07, HT, 90 mm SL, Lombok, S Indonesia (W.T. White); J: the japonicus-group species U. guttatus, SAIAB 13947, 100 mm SL, off Kenya (P.C. Heemstra). Scale bars = 20 mm.

Fig. 7 in Two new species of the Hypostomus cochliodon group (Siluriformes: Loricariidae) from the rio Paraguay basin, with a redescription of Hypostomus cochliodon Kner, 1854

Fig. 7. Spots and color pattern of fins in Hypostomus cochliodon; (a) NUP 12071, 151.1 mm SL, showing spots smaller and closely spaced on head and larger and widely spaced on the body; (b) NUP 12768, 241.1 mm SL, the base of fin with same color of body, becoming dark brown in tip; and uniform spot pattern in ventral portion of body.

Fig. 5 in Two new species of the Hypostomus cochliodon group (Siluriformes: Loricariidae) from the rio Paraguay basin, with a redescription of Hypostomus cochliodon Kner, 1854

Fig. 5. Mouth and teeth of (a) Hypostomus cochliodon, NUP 10807, 208.0 mm SL, showing one series of papillae in inner face of upper and lower jaws; (b) Hypostomus basilisko, holotype, MZUSP 111110, 182.5 mm SL, showing the agglomerated papillae on inner face of upper and lower jaws; and (c) Hypostomus khimaera, MZUSP 111129, holotype, 139.1 mm SL, showing weakly developed papillae not forming series.

Fig. 6 in Two new species of the Hypostomus cochliodon group (Siluriformes: Loricariidae) from the rio Paraguay basin, with a redescription of Hypostomus cochliodon Kner, 1854

Fig. 6. Keels, ridges and odontodes of (a) Hypostomus cochliodon, NUP 10807, 208.0 mm SL, showing two weakly developed ridges in compound pterotic, weakly developed keels, few and weakly developed odontodes and predorsal keels weakly developed; (b) Hypostomus basilisko, holotype, MZUSP 111110, 182.5 mm SL, showing the three ridges on top of head, strongly developed keels, numerous welldeveloped odontodes on plates covering body and head and strong V-shaped predorsal keels; (c) Hypostomus khimaera, holotype, MZUSP 111129, 139.1 mm SL, showing moderately developed keels and dermal plates supporting moderately developed odontodes.

Fig. 12 in Two new species of the Hypostomus cochliodon group (Siluriformes: Loricariidae) from the rio Paraguay basin, with a redescription of Hypostomus cochliodon Kner, 1854

Fig. 12. Sexual dimorphism of Hypostomus basilisko; (a) MNRJ 40184, paratype, 162.3 mm SL, showing pelvic-fin spine with no tumescence in adult female; (b) MNRJ 40184, paratype, 149.1 mm SL, showing a weakly developed tumescence (indicated by arrow) in juvenile male; (c) MZUSP 111110, holotype, 182.5 mm SL, showing well-developed tumescence (indicated by arrow) in adult male.

Fig. 8 in Two new species of the Hypostomus cochliodon group (Siluriformes: Loricariidae) from the rio Paraguay basin, with a redescription of Hypostomus cochliodon Kner, 1854

Fig. 8. Color pattern of live specimen of Hypostomus cochliodon (uncatalogued specimen) from córrego da Onça, Mato Grosso, rio Paraguay basin.

Fig. 4 in Two new species of the Hypostomus cochliodon group (Siluriformes: Loricariidae) from the rio Paraguay basin, with a redescription of Hypostomus cochliodon Kner, 1854

Fig. 4. Lateral view of juvenile in (a) Hypostomus cochliodon, NUP 11956, 92.8 mm SL, (b) Hypostomus basilisko, paratype, ZUFMS-PIS 3083, 64.2 mm SL and (c) Hypostomus khimaera, NUP 13494, 68.8 mm SL.

Fig. 76 in The sumatrana species group of the genus Platyja with descriptions of four new species (Lepidoptera: Erebidae)

Fig. 76 – Distribution of species of the Platyja sumatrana-group (populations from New Britain and Rook Island [= Umboi, Siassi] combined as vityaz s.l.; see explanation in text).

Figs 27-30 in The sumatrana species group of the genus Platyja with descriptions of four new species (Lepidoptera: Erebidae)

Figs 27-30 – Male undersides of Platyja (red lines in figs 27-28 point to main diagnostic features between the two species represented): 27, P. subtracta sp. n.; 28, P. cyanocraspis; 29, P. lecerfi stat. n.; 30, P. sumatrana. Scale bar = 1 cm.

Figs 9-16 in The sumatrana species group of the genus Platyja with descriptions of four new species (Lepidoptera: Erebidae)

Figs 9-16 – Males of Platyja: 9, P. subtracta sp. n., Dampier Island (= Karkar); 10, idem, Fergusson Island; 11, P. vityaz sp. n., holotypus, Rook Island (= Umboi, Siassi); 12, Platyja sp. (vityaz sp. n. or close), New Britain, Talesea; 13, P. yaleyambae sp. n., holotypus, Sudest Island (= Vanatinai, Tagula); 14, idem, paratypus, Sudest Island; 15, idem, Rossel Island (= Yela), Mt Rossel; 16, P. sumatrana, Borneo, Brunei, Bukit Retak. Scale bar = 1 cm.

Figs 17-25 in The sumatrana species group of the genus Platyja with descriptions of four new species (Lepidoptera: Erebidae)

Figs 17-25 – Females of Platyja: 17, P. lecerfi stat. n., syntypus, Moluccas, Seram, Manusela; 18, idem, Moluccas, Buru, Gamoe Mrapat; 19, P. subtracta sp. n., paratypus, New Guinea, near Oetakwa River; 20, idem, paratypus, New Guinea, Ninay Valley; 21, P. cyanocraspis, New Guinea, Ninay Valley; 22, idem, New Guinea, Nomnagihé; 23, P. yaleyambae sp. n., paratypus, Sudest Island (= Vanatinai, Tagula); 24, idem, paratypus, Sudest Island, Mt. Riu; 25, P. sumatrana, Borneo, Sabah, Danum Valley; 26, idem, without locality. Scale bar = 1 cm.

Figs 1-8 in The sumatrana species group of the genus Platyja with descriptions of four new species (Lepidoptera: Erebidae)

Figs 1-8 – Males of Platyja: 1, P. lecerfi stat. n., syntypus, Moluccas, Seram, Manusela; 2, idem, Moluccas, Buru, Kako Tagalago; 3, P. togutila sp. n., holotypus, Moluccas, Halmahera; 4, idem, paratypus, Halmahera; 5, P. subtracta sp. n., holotypus, New Guinea, Hydrographer Mts; 6, idem, paratypus, Hydrographer Mts; 7, P. cyanocraspis, holotypus, New Guinea, near Oetakwa River; 8, idem, topotypus, near Oetakwa River. Scale bar = 1 cm.

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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)