Gastrophryne elegans, (Boulenger, 1882) (Boulenger, 1882)
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https://doi.org/10.11646/zootaxa.5397.1.10 |
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https://doi.org/10.5281/zenodo.17676835 |
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https://treatment.plazi.org/id/FD266B63-C250-475B-FF13-F8DDFD30FA91 |
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Plazi |
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scientific name |
Gastrophryne elegans |
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Tadpole View in CoL description ( Fig. 1 View FIGURE 1 and Table 1 View TABLE 1 ).
The tadpoles of Gastrophryne elegans are exotrophic, lentic, and suspension feeder (guild IIB7; Altig & McDiarmid 1999). In dorsal view, oval body; at Stage 40 the body tends to take a quadrangular form ( Fig. 1A View FIGURE 1 ); in lateral view, body depressed dorsoventrally ( Fig. 1B View FIGURE 1 ). Dorsum straight and rostrum triangular, widening towards the back of the body, reaching its maximum depth at the beginning of the spiracle ( Fig. 1B View FIGURE 1 ). Eyes lateral and pupils oriented laterally. Nostrils closed in nine specimens, evidenced as small slightly dark pigmented protuberances; nostrils opened in one individual at Stage 35, three at 36, two at 37, three at 39, and two at 40; nasolacrimal grooves indistinguishable. Spiracle ventral, medial, tube-shaped extending slightly beyond the body ( Fig. 1C View FIGURE 1 ). Vent tube medial, curved, opening located at the ventral edge of the ventral fin ( Fig. 1C View FIGURE 1 ). Tail relatively long, in average 1.6 times the body length, tip acute ( Fig. 1B View FIGURE 1 ). Tail musculature weakly developed, representing about 15–30% of the maximum body width. Tail fins unequal, the ventral fin slightly deeper, with maximum height close to the middle portion. Dorsal fin originating approximately on the first fifth of the tail. Oral disc terminal, without keratinized elements. Upper labium arched, concave in dorsal view; a pair of smooth flaps pends from the upper lip. The flaps are not parallel but diverging ventrally, in the proximal first quarter are slightly extended towards the front; overall flaps forming an inverted “V” ( Fig. 1D View FIGURE 1 ). Lower lip spatulate with medial labial prominence aligned with medial notch of upper lip.
Coloration. In dorsal view, the color ranges from faint reddish brown to dark brown almost black, with black and yellow to brown very fine reticulations ( Fig. 1A View FIGURE 1 ). The two specimens at Stage 40 exhibit a blotch like a “sandglass” on the dorsum and hindlimbs with black stripes ( Fig. 1A View FIGURE 1 ). The middle ventral body area is dark brown to black, towards the flanks a yellow to white line and pale-yellow blotches towards the central and terminal proportion of the belly. The middle and posterior region contains contrasting black and white reticulations, more contrasting in advanced developmental stages—at Stage 40, the lines, yellow blotches, and contrasting reticulate pattern are more developed. The tail shows a contrasting yellow to orange-pink irregular dorsal stripe extending about 30% over tail in lateral view ( Fig. 1B View FIGURE 1 ). From the middle to the tip, the tail is black with gray blotches with fine black reticulations, the last quarter of the tail, including the fin, almost completely black. Fin with pale orange to pale yellow, gray, and black irregular small blotches; the ventral part of fin with a numerous black spots from the middle towards the end of the tail. In early stages, the proportion of blotches and black color is less on the fin ( Fig. 1B View FIGURE 1 ). Spiracle with black margins and central zone yellow to pale yellow ( Fig. 1A View FIGURE 1 ). Iris black with a thin golden ring bordering the pupil ( Fig. 1B View FIGURE 1 ). In preservative, body dark gray to black, with a distinct white to yellowish stripe clearly visible on the tail.
Natural history. The Zacatal is a temporary lagoon that is filled during the rainy season by the contribution of several temporary streams. This lagoon has an average surface area of 76,453 m 2, a maximum depth of 13 m (average of 7 m), and an annual average oxygen saturation in surface waters of 149% ( Torres-Orozco et al. 1994). On July 11, 2022, we observed a large number (possibly hundreds of thousands) of tadpoles when the lagoon was at approximately 50% of its capacity. We were able to identify tadpoles of Smilisca baudinii (the most abundant), Leptodactylus melanonotus , Lithobates brownorum , L. vaillanti , Rhinella horribilis , and G. elegans , but it was not possible collect tadpoles. The G. elegans tadpoles were the less abundant, we see them floating on the surface and submerged to hide among the flooded vegetation before the slightest disturbance. We observed foraging behavior on the surface and submerged plant leaves. In December 2022, when the lagoon was completely full, we recorded G. elegans tadpoles in a temporary pool ( 2.1 m wide and 0.32 m deep) with a water temperature of 20.1 °C. Although the pool was in the stream, the lagoon’s water surface comprised part of the stream where the tadpoles were observed. During the night, we recorded G. elegans tadpoles submerged and hidden among litter inside the pool, and the substrate was silty. In this month, we also observed some S. baudinii and L. brownorum tadpoles.
Tadpoles of two other species of Gastrophryne are known, G. carolinensis ( Donnelly et al. 1990) and G. olivacea ( Altig & McDiarmid 2015) . Overall, they share many of the typical microhylid-like features, such as a small size, depressed body, medial spiracle opening close to the vent tube, tail fins almost equal, lateral eyes, nostrils mostly closed, keratinized mouthparts lacking, pending oral flaps, and spatulate lower lip. Some features differ among species, with G. olivacea being distinct because of their olive-gray to brown dorsum, white or coppery venter, and lateral tail stripe faint to absent ( Altig & McDiarmid 2015), and G. elegans distinguishable from G. carolinensis by the comparatively smaller eyes and shorter dorsal fin.
Formerly, Hypopachus ustus and H. pictiventris (Cope) were placed within the genus Gastrophryne . Similarities among tadpoles are documented in these two related genera ( Donnelly et al. 1990), and intraspecific variations can complicate species distinction based on larval morphology (e.g., papillated oral flaps are reported in H. variolosus and H. ustus ; Taylor 1942; Nelson & Altig 1972). The inverted V-shape of flaps on the mouth (vs. U-shaped), shorter (vs. along the entire tail) dorsal fin slightly lower than ventral, tail tip pointed, and the body coloration not uniformly black along all developmental stages in our specimens are the main differences with respect to the tadpole described by Nelson & Altig (1972). We consider these authors were correct in their doubtful species assignation, and the specimen they described corresponds more closely to H. ustus . Alternatively, G. elegans could present also wide interpopulation variations. Given their fossorial habits that make them inconspicuous adults, understanding larval morphological variations in G. elegans and other species of Gastrophryne and Hypopachus is a highly valuable tool that can be used to monitor microhylid populations in natural and disturbed areas.
Research carried out thanks to the Program UNAM-DGAPA-PAPIIT number IA209820 granted to VHJA. We thank Rosamond Coates, head of the Estación de Biología Tropical Los Tuxtlas, UNAM, as well as Edgar Quinto and Yovany Cabañas for the logistical support during field work. The field work was carried out under the collection permit granted by the DGVS, Secretaria de Medio Ambiente y Recursos Naturales number 09/K4- 1072/11/21. We appreciate comments and corrections of Florencia Vera and Rafael O. de Sá that substantially improved this work. We especially thank Larry D. Wilson for providing us with specific literature. Thanks to Grupo Acuario Lomas SA de CV for their invaluable donations that support the performance of our laboratory.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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