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178 results for “Leptodactylus”
Figure 3 in Cheliped loss and abnormalities of the narrow-clawed crayfish, Pontastacus leptodactylus (Eschscholtz, 1823) (Crustacea: Decapoda: Astacidae)
Figure 3. Left cheliped abnormalities observed in Pontastacus leptodactylus individuals collected from the Atikhisar Reservoir in Çanakkale, Turkey. Red circles indicate the abnormalities on the left chelipeds
Figure 2 in Cheliped loss and abnormalities of the narrow-clawed crayfish, Pontastacus leptodactylus (Eschscholtz, 1823) (Crustacea: Decapoda: Astacidae)
Figure 2. Right cheliped abnormalities observed in Pontastacus leptodactylus individuals collected from the Atikhisar Reservoir in Çanakkale, Turkey. Red circles indicate the abnormalities on the right chelipeds.
Figure 1 in Cheliped loss and abnormalities of the narrow-clawed crayfish, Pontastacus leptodactylus (Eschscholtz, 1823) (Crustacea: Decapoda: Astacidae)
Figure 1. Map of the sampling area (Atikhisar Reservoir in Çanakkale, Turkey) where Pontastacus leptodactylus individuals were collected. The red triangle indicates the sampling location within the lake.
Figure 4 in Cheliped loss and abnormalities of the narrow-clawed crayfish, Pontastacus leptodactylus (Eschscholtz, 1823) (Crustacea: Decapoda: Astacidae)
Figure 4. Both right and left cheliped abnormalities observed in Pontastacus leptodactylus individuals collected from the Atikhisar Reservoir in Çanakkale, Turkey. Red circles indicate the abnormalities on both right and left chelipeds.
Figure 2 in Effects of methyl farnesoate injection on spermatozoa number and reproductive indices in the narrow-clawed crayfish Pontastacus leptodactylus
Figure 2. Effect of MF injection on reproductive system weight and GSI in male Pontastacus leptodactylus. Letters indicate significant difference groupings (P <0.05) (mean ± S.D; n = 15).
Figure 6 in Estudio histomorfológico comparado del tegumento en Leptodactylus mystacinus y Leptodactylus apepyta (Anura: Leptodactylidae)
Figure 6. Ventral Region of Leptodactylus mystacinus: Epithelium (E); Lax Dermis (DL); Eberth-Katschenko layer (C E-K); Compact Dermis (DC); Hypodermis (H); Mucous Gland (GM); Glandular Canal (Cg). 60x.
Figure 3 in Estudio histomorfológico comparado del tegumento en Leptodactylus mystacinus y Leptodactylus apepyta (Anura: Leptodactylidae)
Figure 3. Ventral Region ofLeptodactylu sapepyta: Epithelium (E); Lax Dermis (DL); Eberth-Katschenko layer (C E-K); Compact Dermis (DC); Hypodermis (H); Serous Gland (GS); Mucous Gland (GM); Connective tissue bridle (Bri). 40x.
Figura 2 in Estudio histomorfológico comparado del tegumento en Leptodactylus mystacinus y Leptodactylus apepyta (Anura: Leptodactylidae)
Figura 2. Región Inguinal de Leptodactylus apepyta: Epitelio (E); Dermis Laxa (DL);Capa Eberth-Katschenko (C E-K); Dermis Compacta (DC); Hipodermis (H); Glándula Serosa (GS); Glándula Mucosa (GM). 40x.
Figure 1 in Estudio histomorfológico comparado del tegumento en Leptodactylus mystacinus y Leptodactylus apepyta (Anura: Leptodactylidae)
Figure 1. Dorsal Region of Leptodactylus apepyta: Epithelium (E); Lax Dermis (DL); Eberth-Katschenko layer (C E-K); Compact Dermis (DC); Hypodermis (H); Serous Gland (GS); Mucous Gland (GM); Chromatophores (Cr). 40x.
Figure 5 in Estudio histomorfológico comparado del tegumento en Leptodactylus mystacinus y Leptodactylus apepyta (Anura: Leptodactylidae)
Figure 5. Inguinal Region of Leptodactylus mystacinus: Epithelium (E); Lax Dermis (DL); Eberth-Katschenko layer (C E-K); Compact Dermis (DC); Hypodermis (H); Serous Gland (GS); Mucous Gland (GM); Chromatophores (Cr). 40x.
Figura 4 in Estudio histomorfológico comparado del tegumento en Leptodactylus mystacinus y Leptodactylus apepyta (Anura: Leptodactylidae)
Figura 4. Región Dorsal de Leptodactylus mystacinus: Epitelio (E); Dermis Laxa (DL); Capa Eberth-Katschenko (C E-K); Dermis Compacta (DC); Hipodermis (H); Glándula Serosa (GS); Glándula Mucosa (GM); Cromatóforos (Cr). 60x.
Figure 2 in A new species, Dactylosoma piperis n. sp. (Apicomplexa, Dactylosomatidae), from the pepper frog Leptodactylus labyrinthicus (Anura, Leptodactylidae) from Mato Grosso State, Brazil.
Figure 2. Consensus phylogram of haemogregarines based on 18S rDNA sequences. The topology trees with Bayesian inference (BI) and Maximum likelihood (ML) analyses were identical (represented by the ML tree). The scale bar represents 0.02 nucleotide substitutions per site. Adelina dimidiata (DQ096835), Adelina grylli (DQ096836), Klossia helicina (HQ224955) and Klossia equi (MH211602) were used as outgroups.
Figure 1. Dactylosoma piperis n in A new species, Dactylosoma piperis n. sp. (Apicomplexa, Dactylosomatidae), from the pepper frog Leptodactylus labyrinthicus (Anura, Leptodactylidae) from Mato Grosso State, Brazil.
Figure 1. Dactylosoma piperis n. sp. in blood smears of Leptodactylus labyrinthicus. Primary merogony (A–F): A) Trophozoite; B) Young primary meront; C–D) Primary large rounded meronts; E–F) Fan-like shaped primary meronts with merozoites. Secondary merogony (G–L): G–H) Young secondary meronts; I–J) Secondary meronts with dactylate appearance; K–L) Secondary meronts with merozoites. Scale bar: 10 µm.
Figure 2. Gorgoderina parvicava Travassos, 1922 in Phylogenetic position of Gorgoderina parvicava Travassos, 1922 (Digenea: Gorgoderidae), a parasite of Leptodactylus labyrinthicus (Spix, 1824) (Anura: Leptodactylidae) in Brazil
Figure 2. Gorgoderina parvicava Travassos, 1922 (Gorgoderidae) parasite ofLeptodactylus labyrinthicus (Spix, 1824) (Leptodactylidae) from Carandá Farm, municipality of Araraquara, São Paulo state, Brazil. A) Detail of the oral sucker, oesophagus, and intestinal caeca; B) Acetabulum; C) Detail of the region of seminal vesicle and metraterm; D) Detail of the terminal genitalia and metraterm, highlighting the genital pore (left above corner); E) Ovary; F) Region of the ovary highlighting the Mehlis' gland and vitelline follicles; G) Detail of the Mehlis' gland; H) Eggs in the uterus, highlighting part of the descending loop of the uterus with immature eggs and an ascending part with mature eggs. Legend: ac – acetabulum, gp – genital pore, ic – intestinal caeca, ig – immature eggs, m – metraterm, me – mature eggs, mg – Mehlis' gland, mo – mature oocytes, od – ovary duct, oe – oesophagus, os – oral sucker, ov – ovary, pp – pars prostatica, sv – seminal vesicle, t – testis, u – uterus, vd – vitelline ducts, vi – vitelline follicles.
Figure 3 in Phylogenetic position of Gorgoderina parvicava Travassos, 1922 (Digenea: Gorgoderidae), a parasite of Leptodactylus labyrinthicus (Spix, 1824) (Anura: Leptodactylidae) in Brazil
Figure 3. Maximum Likelihood topology based on partial 28S ribosomal DNA sequences of gorgoderid trematodes. GenBank accession numbers are indicated next to species names. Numbers above nodes represent supported nodes by posterior probabilities for Bayesian Bayesian inference and bootstrap for maximum likelihood analyses respectively (posterior probabilities> 0.90 and bootstrap scores> 70). Branch length scale bar indicates the number of substitutions per site.
Figure 4 in Phylogenetic position of Gorgoderina parvicava Travassos, 1922 (Digenea: Gorgoderidae), a parasite of Leptodactylus labyrinthicus (Spix, 1824) (Anura: Leptodactylidae) in Brazil
Figure 4. Maximum Likelihood topology based on COI sequences of Gorgoderina, showing the phylogenetic position of the adults of Gorgoderina parvicava from Carandá Farm, municipality of Araraquara, São Paulo State, Brazil. Numbers above nodes represent supported nodes by posterior probabilities for Bayesian Bayesian inference and bootstrap for maximum likelihood analyses respectively (posterior probabilities> 0.90 and bootstrap scores> 70). Branch length scale bar indicates the number of substitutions per site.
Figure 1. Gorgoderina parvicava Travassos, 1922 in Phylogenetic position of Gorgoderina parvicava Travassos, 1922 (Digenea: Gorgoderidae), a parasite of Leptodactylus labyrinthicus (Spix, 1824) (Anura: Leptodactylidae) in Brazil
Figure 1. Gorgoderina parvicava Travassos, 1922 (Gorgoderidae) parasite ofLeptodactylus labyrinthicus (Spix, 1824) (Leptodactylidae) from Carandá Farm, municipality of Araraquara, São Paulo state, Brazil. Ventral view.
Fig. 3 in Development of in-country live food production for amphibian conservation: The Mountain Chicken Frog (Leptodactylus fallax) on Dominica, West Indies
Fig. 3. (A) Two rows of cricket breeding containers and cockroach breeding bins below. (B) Inside of a cricket breeding container, including refugia, food items, and several egg laying containers, transplanted into an empty container to allow eggs to hatch. (C) Inside view of a cockroach breeding bin, including substrate, refugia, and several food items. Photos: D. Nicholson.
Fig. 2 in Development of in-country live food production for amphibian conservation: The Mountain Chicken Frog (Leptodactylus fallax) on Dominica, West Indies
Fig. 2. Cultured species at the CBP in Dominica. (A) Gryllodes sigillatus. (B) Gryllus assimilis. (C) Caribacusta dominica. (D) Blaberus discoidalis. (E) Zophobas atratus. (F) Veronicella sloanii. (G) Pleurodonte dentiens. (H) Leptogoniulus sp. Photos: D. Nicholson.
Figure 6 in On the natural history of the South American pepper frog, Leptodactylus labyrinthicus (Spix, 1824) (Anura: Leptodactylidae)
Figure 6. Combat between males of Leptodactylus labyrinthicus. These males were in position to grasp each other. Observation in Uberlândia, MG, Brazil.
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