Genetic diversity, demographic history and neo-sex chromosomes in the critically endangered Raso lark

• Published in: Proceedings of the Royal Society B: Biological Sciences
• Main Authors: Dierickx, Elisa G., Sin, Simon Yung Wa, van Veelen, H. Pieter J., Brooke, M. de L., Liu, Yang, Edwards, Scott V., Martin, Simon H.
• Format: Article in Journal/Newspaper
• Language: English
• Published: 2020
• Subjects: recombination suppression; Alauda; conservation; Cape Verde; island endemic; demography; POPULATION-SIZE; ALAUDA-RAZAE; EXTINCTION; EVOLUTION; GENOMES; RISK; Eurasian Skylark
• Online Access: https://hdl.handle.net/11370/af634268-d010-4a30-9338-81aee2fababc; https://research.rug.nl/en/publications/af634268-d010-4a30-9338-81aee2fababc; https://doi.org/10.1098/rspb.2019.2613; https://pure.rug.nl/ws/files/133209877/rspb.2019.2613.pdf

Small effective population sizes could expose island species to inbreeding and loss of genetic variation. Here, we investigate factors shaping genetic diversity in the Raso lark, which has been restricted to a single islet for approximately 500 years, with a population size of a few hundred. We assembled a reference genome for the related Eurasian skylark and then assessed diversity and demographic history using RAD-seq data (75 samples from Raso larks and two related mainland species). We first identify broad tracts of suppressed recombination in females, indicating enlarged neo-sex chromosomes. We then show that genetic diversity across autosomes in the Raso lark is lower than in its mainland relatives, but inconsistent with long-term persistence at its current population size. Finally, we find that genetic signatures of the recent population contraction are overshadowed by an ancient expansion and persistence of a very large population until the human settlement of Cape Verde. Our findings show how genome-wide approaches to study endangered species can help avoid confounding effects of genome architecture on diversity estimates, and how present-day diversity can be shaped by ancient demographic events.