TL;DR: An integrative analysis of two independent Amazonian frog clades, Engystomops toadlets and Hypsiboas treefrogs, suggests that Amazonianfrog biodiversity is much more severely underestimated than previously thought.
Abstract: One of the greatest challenges for biodiversity conservation is the poor understanding of species diversity. Molecular methods have dramatically improved our ability to uncover cryptic species, but the magnitude of cryptic diversity remains unknown, particularly in diverse tropical regions such as the Amazon Basin. Uncovering cryptic diversity in amphibians is particularly pressing because amphibians are going extinct globally at an alarming rate. Here, we use an integrative analysis of two independent Amazonian frog clades, Engystomops toadlets and Hypsiboas treefrogs, to test whether species richness is underestimated and, if so, by how much. We sampled intensively in six countries with a focus in Ecuador (Engystomops: 252 individuals from 36 localities; Hypsiboas: 208 individuals from 65 localities) and combined mitochondrial DNA, nuclear DNA, morphological, and bioacoustic data to detect cryptic species. We found that in both clades, species richness was severely underestimated, with more undescribed species than described species. In Engystomops, the two currently recognized species are actually five to seven species (a 150‐ 250% increase in species richness); in Hypsiboas, two recognized species represent six to nine species (a 200‐350% increase). Our results suggest that Amazonian frog biodiversity is much more severely underestimated than previously thought.
TL;DR: This work reports on the early development, rearing, and embryological analysis of túngara frogs (genus Engystomops), also called Physalaemus, which are attractive for comparative and genetic studies of development.
TL;DR: Results show that geographic variation in predation may play an important role in the evolution and maintenance of mating signal divergence and suggest selection against complex calls in Engystomops petersi.
Abstract: Sexual selection plays an important role in mating signal divergence, but geographic variation in ecological factors can also contribute to divergent signal evolution. We tested the hypothesis that geographic heterogeneity in predation causes divergent selection on advertisement call complexity within the Engystomops petersi (previously Physalaemus petersi) frog species complex. We conducted predator phonotaxis experiments at two sites where female choice is consistent with call trait divergence. Engystomops at one site produces complex calls, whereas the closely related species at the other site produces simple calls. Bats approached complex calls more than simple calls at both sites, suggesting selection against complex calls. Moreover, bat predation pressure was greater at the site with simple calls, suggesting stronger selection against complex calls and potentially precluding evolution of complex calls at this site. Our results show that geographic variation in predation may play an important role in the evolution and maintenance of mating signal divergence.
TL;DR: Female tungara frogs, two eavesdroppers, frog-eating bats, Trachops cirrhosus, and blood-sucking flies, Corethrella spp.
Abstract: Sexual selection is responsible for the evolution of extreme and elaborate sexual dimorphisms. This is especially true for communication systems involved in mate attraction. Anurans, in general, and tungara frogs (Physalaemus pustulosus), in particular, have emerged as an ideal model for studies of sexual selection and communication. Male tungara frogs gather in choruses and vocally advertise for females with a long-distance advertisement call. The call consists of whine that can be followed by 0–7 chucks; only the sister taxa of the tungara frog are known to produce similarly variably complex calls. Male tungara frogs add chucks in response to the vocalizations of other males, and females are more attracted to calls with chucks than calls without chucks. Females move about the chorus and choose a mate with minimum interference from males. Females are more likely to choose larger males, and this preference results from their preference for the lower-frequency chucks produced by larger males. The preference for lower-frequency chucks, in turn, results from the relationship between the average tuning of the female’s inner ear and the average dominant frequency of the chuck. The female’s basilar papilla is more sensitive to chucks with lower-than-average compared to higher-than-average frequencies. The tuning of this inner ear organ did not evolve in tungara frogs but also characterizes most of its close relatives; this suggests that aspects of the chuck evolved to match preexisting sensory biases in females. The communication system of tungara frogs does not occur in a private channel. As do female tungara frogs, two eavesdroppers, frog-eating bats, Trachops cirrhosus, and blood-sucking flies, Corethrella spp., also use the mating call to localize males, but in these cases the eavesdroppers either eat them or suck their blood. Furthermore, as with the female frogs, the eavesdroppers are attracted preferentially to complex calls over simple calls. This exemplifies the conflict between natural selection and sexual selection highlighted by Darwin.