18PCR-based methods are the most common technique for sex determination of birds. 19Although these methods are fast, easy and accurate, they still require special facilities 20 that preclude their application outdoors. Consequently, there is a time lag between 21 sampling and obtaining results that impedes researchers to take decisions in situ and in 22 real time considering individuals' sex. We present an outdoor technique for sex 23 determination of birds based on the amplification of the duplicated sex-chromosome-24 specific gene Chromo-Helicase-DNA binding protein using a Loop-Mediated 25Isothermal Amplification (LAMP). We tested our method on Griffon Vulture (Gyps 26 fulvus), Egyptian Vulture (Neophron percnopterus) and Black Kite (Milvus migrans) 27 (family Accipitridae). We introduce the first fieldwork procedure for sex determination 28 of animals in the wild, successfully applied to raptor species of three different 29 subfamilies using the same specific LAMP primers. This molecular technique can be 30 deployed directly in sampling areas since it only needs a voltage inverter to adapt a 31 thermo-block to a car lighter and results can be obtained by the unaided eye based on 32 colour change within the reaction tubes. Primers and reagents are prepared in advance 33 to facilitate their storage at room temperature. We provide detailed guidelines how to 34 implement this procedure, which is simpler (no electrophoresis required), cheaper and 35 faster (results in ca. 90 minutes) than PCR-based laboratory methods. Our successful 36 cross-species application across three different raptor subfamilies posits our set of 37 markers as a promising tool for molecular sexing of other raptor families and our field 38 protocol extensible to all bird species.