individual_fastq.zipRaw fastq files for each individual. Libraries prepared using Best RADseq method
inputs-scripts.tar.gz
Scripts for generating input files from raw sequence data sample-info_phenotypes.xlsxLeg color data used for color similarity analysis (tab:all_phenotyped_RGB%) and for genome-wide association analysis (tab:genotyped&phenotyped). RGB values and percent of pixels in each color bin generated with colordistance package in R.

individual_fastq.zipRaw fastq files for each individual. Libraries prepared using Best RADseq method

sample-info_phenotypes.xlsxLeg color data used for color similarity analysis (tab:all_phenotyped_RGB%) and for genome-wide association analysis (tab:genotyped&phenotyped). RGB values and percent of pixels in each color bin generated with colordistance package in R.

individual_fastq.zipRaw fastq files for each individual. Libraries prepared using Best RADseq method
inputs-scripts.tar.gz
Scripts for generating input files from raw sequence data sample-info_phenotypes.xlsxLeg color data used for color similarity analysis (tab:all_phenotyped_RGB%) and for genome-wide association analysis (tab:genotyped&phenotyped). RGB values and percent of pixels in each color bin generated with colordistance package in R.

We examined courtship behaviour of 15–20 females from each of four populations of red-eyed treefrogs. We measured mating behaviour using a no-choice experimental design. Females were tested in three 10-min trials in which she was presented, in random order, with a model from the local or one of two non-local populations. We recorded the occurrence of back and/or flank displays and time invested in flank display. Due to the uniformly short duration of back displays (<3 s), we did not measure duration for this trait. We recorded the advertisement calls of 12–22 males from each of six populations of red-eyed treefrogs. We determined the dominant frequency and the interquartile range bandwidth (bandwidth; the frequency range containing the middle 50% of sound energy) using Raven 1.4.We also include data from mate choice trials conducted by Jacobs et al. in 2013 using live males and females. For methods, see: Jacobs, L. E., Vega, A., Dudgeon, S., Kaiser, K., & Robertson, J. M. (2016). Local not vocal: assortative female choice in divergent populations of red‐eyed treefrogs, Agalychnis callidryas (Hylidae: Phyllomedusinae). Biological Journal of the Linnean Society.

We examined courtship behaviour of 15–20 females from each of four populations of red-eyed treefrogs. We measured mating behaviour using a no-choice experimental design. Females were tested in three 10-min trials in which she was presented, in random order, with a model from the local or one of two non-local populations. We recorded the occurrence of back and/or flank displays and time invested in flank display. Due to the uniformly short duration of back displays (<3 s), we did not measure duration for this trait. We recorded the advertisement calls of 12–22 males from each of six populations of red-eyed treefrogs. We determined the dominant frequency and the interquartile range bandwidth (bandwidth; the frequency range containing the middle 50% of sound energy) using Raven 1.4.We also include data from mate choice trials conducted by Jacobs et al. in 2013 using live males and females. For methods, see: Jacobs, L. E., Vega, A., Dudgeon, S., Kaiser, K., & Robertson, J. M. (2016). Local not vocal: assortative female choice in divergent populations of red‐eyed treefrogs, Agalychnis callidryas (Hylidae: Phyllomedusinae). Biological Journal of the Linnean Society.

We examined courtship behaviour of 15–20 females from each of four populations of red-eyed treefrogs. We measured mating behaviour using a no-choice experimental design. Females were tested in three 10-min trials in which she was presented, in random order, with a model from the local or one of two non-local populations. We recorded the occurrence of back and/or flank displays and time invested in flank display. Due to the uniformly short duration of back displays (<3 s), we did not measure duration for this trait. We recorded the advertisement calls of 12–22 males from each of six populations of red-eyed treefrogs. We determined the dominant frequency and the interquartile range bandwidth (bandwidth; the frequency range containing the middle 50% of sound energy) using Raven 1.4.

We examined courtship behaviour of 15–20 females from each of four populations of red-eyed treefrogs. We measured mating behaviour using a no-choice experimental design. Females were tested in three 10-min trials in which she was presented, in random order, with a model from the local or one of two non-local populations. We recorded the occurrence of back and/or flank displays and time invested in flank display. Due to the uniformly short duration of back displays (<3 s), we did not measure duration for this trait. We recorded the advertisement calls of 12–22 males from each of six populations of red-eyed treefrogs. We determined the dominant frequency and the interquartile range bandwidth (bandwidth; the frequency range containing the middle 50% of sound energy) using Raven 1.4.