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Stephanie N Caty

Publications and source records attributed to Stephanie N Caty.

2 recordsLinked to original sources

Radiation and hybridization of the Little Devil poison frog (Oophaga sylvatica) in Ecuador

Geographic variation of color pattern in the South American poison frogs (Dendrobatidae) is an intriguing evolutionary phenomenon. These chemically defended anurans use bright aposematic colors to warn potential predators of their unpalatibility. However, aposematic signals are frequency-dependent and individuals deviating from a local model are at a higher risk of predation. The well-known examples of Batesian and Mullerian mimics, hymenopterans (wasps and bees) and Heliconius butterflies, both support the benefits of unique models with relatively high frequencies. However, extreme diversity in the aposematic signal has been documented in the poison frogs of the genus Dendrobates, especially in the Oophaga subgenus. Here we investigate the phylogenetic and genomic differentiations among populations of Oophaga sylvatica, which exhibit one of the highest phenotypic diversification among poison frogs. Using a combination of PCR amplicons (mitochondrial and nuclear markers) and genome wide markers from a double-digested RAD data set, we characterize 13 populations (12 monotypic and 1 polytypic) across the O. sylvatica distribution. These populations are mostly separated in two lineages distributed in the Northern and the Southern part of their range in Ecuador. We found relatively low genetic differentiation within each lineage, despite considerable phenotypic variation, and evidence suggesting ongoing gene flow and genetic admixture among some populations of the Northern lineage. Overall these data suggest that phenotypic diversification and novelty in aposematic coloration can arise in secondary contact zones even in systems where phenotypes are subject to strong stabilizing selection.

Evolutionary Biology

Ant and mite diversity drives toxin variation in the Little Devil poison frog

Poison frogs sequester chemical defenses from arthropod prey, although the details of how arthropod diversity contributes to variation in poison frog toxins remains unclear. We characterized skin alkaloid profiles in the Little Devil frog, Oophaga sylvatica (Dendrobatidae), across three populations in northwestern Ecuador. Using gas chromatography mass spectrometry, we identified histrionicotoxins, 3,5- and 5,8-disubstituted indolizidines, decahydroquinolines, and lehmizidines as the primary alkaloid toxins in these O. sylvatica populations. Frog skin alkaloid composition varied along a latitudinal gradient across populations in a principal component analysis. We also characterized diversity in arthropods isolated from frog stomach contents and confirmed O. sylvatica specialize on ants and mites. To test the hypothesis that poison frog toxin diversity reflects species and chemical diversity in arthropod prey, we (1) used liquid chromatography mass spectrometry to chemically profile consumed ants and mites, and (2) used sequencing of cytochrome oxidase 1 to identify individual prey specimens. We show that chemical profiles of consumed ants and mites cluster by frog population, suggesting different frog populations have access to chemically distinct prey. We identified 45 ants and 9 mites isolated from frog stomachs, finding several undescribed species. Finally, by comparing chemical profiles of frog skin and isolated prey items, we were able to trace the arthropod source of four poison frog alkaloids, including 3,5- and 5,8-disubstituted indolizidines and a lehmizidine alkaloid. Together, our data shows the diversity of alkaloid toxins found in O. sylvatica can be traced to chemical diversity in arthropod prey.

Preprint