Evaluating molecular and behavioural sexing methods for the Australasian gannet (Morus serrator)

Abstract

The availability of molecular methods for avian sex identification has revolutionised the study of sexual differences in behaviour, morphology, life-history traits and conservation management. We implemented the recommendations of a recent review of DNA-based sex-identification by (1) verifying the sex-specificity and (2) estimating the accuracy of different sex-assignment methods in an apparently monomorphic seabird, the Australasian gannet (Morus serrator). The polymerase chain reaction (PCR) method based on the amplification of the sex-linked chromodomain-helicase-DNA binding gene (CHD) repeatedly assigned the same sex in 96% (n = 27 replicates) and correctly sexed all individuals with known gonadal anatomy (n = 6). PCR and sex-specific restriction fragment length polymorphism (RFLPs) showed agreement for 99.5% of individuals (n = 201). DNA-sexed pairs known to be social mates consisted of a male and a female in 96% of pairs sexed by PCR (n = 77) and 98% of pairs sexed by RFLP (n = 65). DNA-sexed females were in the bottom and males in the top copulatory position in 86% of observed copulations (n = 43 individuals). These results validate assumptions that both membership in social pairs and different copulatory positions can serve as reliable behavioural proxies for field-based sex identification in this colonial and obligately biparental seabird.