SUMMARYAnuran larvae, which are otherwise simple in shape, typically have complex keratinized mouthparts (i.e. labial teeth and jaw sheaths) that allow them to graze upon surfaces. The diversity in these structures among species presumably reflects specializations that allow for maximal feeding efficiency on different types of food. However, we lack a general understanding of how these oral structures function during feeding. We used high-speed digital imaging (500Hz) to observe tadpoles of six species from the anuran family Hylidae grazing on a standardized food-covered substrate. Tadpoles of these species vary in the number of labial tooth rows, belong to two different feeding guilds (benthic and nektonic), and inhabit ponds and streams. We confirmed that the labial teeth in these species serve two functions: anchoring the mouth to the substrate and raking material off of the substrate. In general, tadpoles with a larger maximum gape or those with fewer labial tooth rows opened and closed their mouths slower than tadpoles with smaller gape or more tooth rows. Nektonic feeding tadpoles released each of their tooth rows proportionally earlier in the gape cycle compared with benthic feeding tadpoles. Lastly, we found some support for the idea that deformation of the jaw sheaths during a feeding cycle is predictable based on tadpole feeding guild. Collectively, our data show that anatomical (e.g. number of labial teeth) and ecological features (e.g. feeding guild) of tadpoles significantly influence how tadpoles open and close their mouths during feeding. Supplementary material available online at
In nature, tadpoles encounter food on substrates oriented at different angles (e.g. vertically along stems, horizontally on the bottom of the pond). We manipulated the orientation of food-covered surfaces to test how different orientations of surfaces affect tadpoles' feeding efficiency. We studied taxa that differed in the oral morphology of their larvae and position in the water column. We hypothesized that species would differ in their ability to graze upon surfaces at different orientations and that differences in the tadpoles' feeding ability would result in different growth rates. The orientation of food-covered surfaces did not affect the growth rate of bottom-dwelling tadpoles (whose growth rate varied only between species). Among midwater tadpoles, some species appear to have a generalist strategy and experienced a high relative growth rate on numerous substrate orientations, whereas others achieved high growth rates only on flat substrates (i.e. at 0° and 180°). We conclude that oral morphology constrains tadpoles' ability to feed at different substrate orientations, and this could lead to niche partitioning in structurally complex aquatic environments. Because physical parameters of the environment can affect tadpoles' growth rate, characterizing these features might help us better understand how competition structures tadpole assemblages.
Temperature impacts ectotherm performance by influencing many biochemical and physiological processes. When well adapted to their environment, ectotherms should perform most efficiently at the temperatures they most commonly encounter. In the present study, we tested how differences in temperature affects the feeding kinematics of tadpoles of two anuran species: the benthic tadpole of Rhinella schneideri and the nektonic tadpole of Trachycephalus typhonius. Benthic and nektonic tadpoles have segregated distributions within ponds and thus tend to face different environmental conditions, such as temperature. Muscle contractile dynamics, and thus whole organism performance, is primarily temperature dependent for ectotherms. We hypothesized that changes in mean temperatures would have differential effects on the feeding kinematics of these two species. We conducted a laboratory experiment in which we used high-speed videography to record tadpoles foraging at cold and warm temperatures. In general, tadpoles filmed at warm temperatures opened their jaws faster, attained maximum gape earlier, and exhibited shorter gape cycles than tadpoles in cold temperatures, irrespective of species. We also found species x temperature interactions regarding the closing phase velocity, and the percentage of time it takes tadpoles to achieve maximum gape and to start closing their jaws. These interactions could indicate that these two co-occurring species differ in their sensitivity to differences in water temperature and have temperature-dependent feeding strategies that maximize feeding performance in their preferred environment.
Leptodactylus labyrinthicus tadpoles are known predators of anuran eggs and hatchlings, but they are also able to filter-feed in the water column and scrape food off of firm substrates. We evaluated and compared these alternative feeding behaviors in relation to feeding kinematics and the shape of the mouth with high-speed digital imaging. We tested the hypotheses that (1) L. labyrinthicus tadpoles use functionally different feeding kinematics when feeding on alternative food sources and (2) that the jaw sheaths of L. labyrinthicus tadpoles deform less during filter-feeding and substrate grazing compared with more common tadpoles not so specialized for macrophagous carnivory. Our results show that filtering and scraping feeding behaviors differ significantly in both kinematics and shape of the mouth. During filter-feeding, tadpoles display longer gape cycles and attain a narrower maximum gape earlier in the cycle compared with substrate grazing. Jaw deformation during opening and closing phases of the gape cycle is more pronounced during grazing on firm substrates. This deformation contributes to the achievement of a wider maximum gape during feeding. These differences appear to reflect behavioral adjustments by the tadpoles to maximize food intake. Feeding in tadpoles of L. labyrinthicus is not restrained by their typical carnivorous morphology. On the contrary, L. labyrinthicus tadpoles seem to be opportunistic feeders able to obtain nutrients from a variety of food sources by using different feeding strategies.
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