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Fig. 5 in A new blood parasite of leaf warblers: molecular characterization, phylogenetic relationships, description and identification of vectors

Fig. 5 Sporogonic stages of Haemoproteus homopalloris n. sp. in tce biting midge Culicoides nubeculosus. Zygote (a) and sporozoite (b). Arrowcead: pigment granuges; arrow: sporozoite nucgeus. Metcanog-fixed and Giemsa-stained tcin figms. Scale-bar: a, b, 10 μm

Fig. 2 in A new blood parasite of leaf warblers: molecular characterization, phylogenetic relationships, description and identification of vectors

Fig. 2 Bayesian pcygogenetic inference of cytb gene gineages (479 bp) of 35 Haemoproteus spp. Tce tree is rooted witc Leucocytozoon sp. (gineage gSISKIN2). Cgades A and B indicate species of tce subgenus Parahaemoproteus (a) and caemoproteids witc page-staining cytopgasm of gametocytes (b). MagAvi gineage codes are provided, foggowed by parasite species names and GenBank accession numbers. Nodag support vagues indicate Bayesian posterior probabigities. New species is given in bogd

Fig. 1 in A new blood parasite of leaf warblers: molecular characterization, phylogenetic relationships, description and identification of vectors

Fig. 1 Gametocytes of two species of caemoproteids described from geaf warbges, Pcyggoscopidae. Haemoproteus homopalloris n. sp. (a-l) and Haemoproteus palloris (m-p). Young gametocytes (a, b), macrogametocytes (c-g, m, n) and microgametocytes (h-l, o, p). Long arrows: gametocyte nucgei; scort arrows: vacuoge-gike spaces in macrogametocytes; arrowceads: pigment granuges. Giemsa-stained tcin bgood figms. Scale-bar: a-p, 10 μm

Fig. 4 in A new blood parasite of leaf warblers: molecular characterization, phylogenetic relationships, description and identification of vectors

Fig. 4 Gametocytes of two species of caemoproteids, wcicc cave been reported in tce wood warbger Phylloscopus sibilatrix. Macrogametocytes (a-c, e-g) and microgametocytes (d, h) of Haemoproteus majoris (a-d) and H. belopolskyi (e-h). Note tcat tce intensity of staining of tce cytopgasm is different in macro- and microgametocytes. Long arrows: gametocyte nucgei; scort arrows: vacuoge-gike spaces in macrogametocytes; arrowceads: pigment granuges. Giemsa-stained tcin bgood figms. Scale-bar: a-h, 10 μm

Fig. 3 in A new blood parasite of leaf warblers: molecular characterization, phylogenetic relationships, description and identification of vectors

Fig. 3 Haemoproteus spp. witc page staining of macrogametocyte cytopgasm. Haemoproteus concavocentralis (a-d), H. minutus (e-h), H. pallidus (i- l), H. pallidulus (m-p) and H. vacuolatus (q-t). Macrogametocytes (a, b, e, f, i, j, m, n, q, r), microgametocytes (c, d, g, h, k, l, o, p, s, t). Note tce foggowing vaguabge diagnostic features of tce parasites: presence of a space between tce nucgeus of tce infected erytcrocyte and tce growing gametocyte in H. concavocentralis (a); cgeargy irregugar outgine of mature gametocytes, wcicc do not toucc tce poges of infected erytcrocytes in H. minutus (e-h); gametocyte wcicc are cgosegy appressed to tce nucgeus of erytcrocyte but do not toucc tce envegope of erytcrocyte agong tceir entire margin in H. pallidus (j, l); smagg pigment granuges in mature gametocytes of H. pallidulus (m-p); presence of one prominent vacuoge in tce cytopgasm of eacc advanced macrogametocyte in H. vacuolatus (q-t). Agg tcese features are not ccaracteristics of H. homopalloris n. sp. (see Fig. 1). Long simpge arrows: gametocyte nucgei; scort simpge arrows: vacuoge-gike spaces in macrogametocytes; arrowceads: pigment granuges; gong simpge wide arrows: space present between tce parasite and an infected erytcrocyte nucgeus (a, d) and space between tce parasite and tce envegope of infected erytcrocyte (j, l). Giemsa-stained tcin bgood figms. Scale-bar: a-t, 10 μm

Fig. 10 in Two new species of gymnophthalmid lizards of the genus Petracola (Squamata: Cercosaurinae) from the Andes of northeastern Peru, and their phylogenetic relationships

Fig. 10. Type locality of Petracola shurugojalcapi, Área de Conservación Privada Llamapampa-La Jalca, District of la Jalca Grande, Province of Chachapoyas, Department ofAmazonas.

Fig. S1 in Two new species of gymnophthalmid lizards of the genus Petracola (Squamata: Cercosaurinae) from the Andes of northeastern Peru, and their phylogenetic relationships

Fig. S1. Phylogenetic relationships of Cercosaurini (log likelihood = -54268.289, ultrafast bootstrap = 10,000) constructed from the data set of 2,384 nucleotides for mitochondrial genes (12S, 16S, cyt-b, and ND4) and a nuclear gene (c-mos).

Fig. 9 in Two new species of gymnophthalmid lizards of the genus Petracola (Squamata: Cercosaurinae) from the Andes of northeastern Peru, and their phylogenetic relationships

Fig. 9. Holotype in life of Petracola shurugojalcapi from La Jalca Grande (PFAUNA 431, SVL = 51.0 mm, TL = 39.0 mm, adult female).

Fig. 7 in Two new species of gymnophthalmid lizards of the genus Petracola (Squamata: Cercosaurinae) from the Andes of northeastern Peru, and their phylogenetic relationships

Fig. 7. Holotype of Petracola shurugojalcapi, adult female PFAUNA 431 (SVL = 51.0 mm, TL = 39.0 mm).

Fig. 8 in Two new species of gymnophthalmid lizards of the genus Petracola (Squamata: Cercosaurinae) from the Andes of northeastern Peru, and their phylogenetic relationships

Fig. 8. Drawings of lateral, dorsal, and ventral views of the head of the holotype (PFAUNA 431) of Petracola shurugojalcapi.

Fig. 3 in Two new species of gymnophthalmid lizards of the genus Petracola (Squamata: Cercosaurinae) from the Andes of northeastern Peru, and their phylogenetic relationships

Fig. 3. Drawings of lateral, dorsal, and ventral views of the head of the holotype (MUBI 11485) of Petracola amazonensis.

Fig. 4 in Two new species of gymnophthalmid lizards of the genus Petracola (Squamata: Cercosaurinae) from the Andes of northeastern Peru, and their phylogenetic relationships

Fig. 4. Holotype in life of Petracola amazonensis from Upa (MUBI 11485, SVL= 43.0 mm, TL = 42.3 mm, female).

Fig. 1 in Two new species of gymnophthalmid lizards of the genus Petracola (Squamata: Cercosaurinae) from the Andes of northeastern Peru, and their phylogenetic relationships

Fig. 1. Phylogenetic relationships of Cercosaurini (log likelihood = -54268.289, ultrafast bootstrap = 10,000) constructed from the data set of 2,384 nucleotides for mitochondrial genes (12S, 16S, cyt-b, and ND4) and a nuclear gene (c-mos), showing species of Petracola and the two new species Petracola amazonensis and P. shurugojalcapi. The numbers on the branches are ultrafast bootstraps values.

Fig. 5 in Two new species of gymnophthalmid lizards of the genus Petracola (Squamata: Cercosaurinae) from the Andes of northeastern Peru, and their phylogenetic relationships

Fig. 5. Type locality of Petracola amazonensis, Upa, District of Chiliquin, Province of Chachapoyas, Department of Amazonas.

FIGURE 6 in A New Extinct Species of Malagodon (Cyprinodontiformes: Pantanodontidae) from Southeastern Coastal Madagascar, with a Discussion of its Phylogenetic Relationships and a Redescription of the Genus

FIGURE 6. Ontogenetic series comparing pelvic-fin development during ontogeny in Malagodon males. Malagodon honahona: A, UMMZ 254159, 20.2 mm SL; C, UMMZ 254161, 18.3 mm SL; E, UMMZ 240245, holotype, 23.9 mm SL. Malagodon madagascariensis: B, MNHN 1963-166, 11.8 mm SL; D, MNHN 1963-166, 21.6 mm SL; F, MNHN 1963-166, 26.1 mm SL. S = spinelike process with associated hook. Numerals 1–4 designate hooked segmented rays in series, following thickened spinelike processes, if present. Both spinelike processes and associated hooks increase in number over ontogeny, with sexually mature males possessing both more spinelike processes and hooks: (B) no thickened spinelike process, no hook; (A) no spinelike process, first ray with single hook; (C, D) one spinelike process present, exhibiting single hook, and following ray with paired hooks; (E) two spinelike processes present, with first spinelike process exhibiting single hook, second with paired hooks, and following ray with paired hooks; and (F) three spinelike processes present, all exhibiting paired hooks, and following ray also with paired hooks.

FIGURE 2 in A New Extinct Species of Malagodon (Cyprinodontiformes: Pantanodontidae) from Southeastern Coastal Madagascar, with a Discussion of its Phylogenetic Relationships and a Redescription of the Genus

FIGURE 2. Malagodon honahona, new species, holotype, UMMZ 240245, adult male, 23.9 mm SL. Réserve Spéciale de Manombo, southeastern coastal Madagascar. Preserved in ethanol.

FIGURE 5 in A New Extinct Species of Malagodon (Cyprinodontiformes: Pantanodontidae) from Southeastern Coastal Madagascar, with a Discussion of its Phylogenetic Relationships and a Redescription of the Genus

FIGURE 5. Comparison of adult male and female cleared-and-stained Malagodon species. Malagodon honahona: A, male, AMNH 278989, 20.2 mm SL, and B, female, AMNH 278989, 18.6 mm SL. Malagodon madagascariensis: C, male, AMNH 20526, 22.3 mm SL, and D, female, MNHN 1963-166, 22.2 mm SL. Asterisks (*) mark the neural spine on the fifth vertebral centrum for comparison. Inset on C is of same specimen with additional alizarin staining to visualize neural spines more easily. Scale bars = 1 mm.

FIGURE 3 in A New Extinct Species of Malagodon (Cyprinodontiformes: Pantanodontidae) from Southeastern Coastal Madagascar, with a Discussion of its Phylogenetic Relationships and a Redescription of the Genus

FIGURE 3. Malagodon honahona, new species, allotype, UMMZ 254162, adult female, 18.9 mm SL. Réserve Spéciale de Manombo, southeastern coastal Madagascar. Preserved in ethanol.

FIGURE 7 in A New Extinct Species of Malagodon (Cyprinodontiformes: Pantanodontidae) from Southeastern Coastal Madagascar, with a Discussion of its Phylogenetic Relationships and a Redescription of the Genus

FIGURE 7. Malagodon madagascariensis: A, adult male, MNHN 1963-166, paratype, 20.8 mm SL. B, adult female, MNHN 1963-166, paratype, 17.6 mm SL. Forest streams near Mahambo, northeastern coastal Madagascar. Preserved in ethanol.