“…The medial amygdala and BSTM of sauropsids show patterns of connections similar to those of mammalian EAme, such as inputs from the olfactory/vomerolfactory bulbs [Reiner and Karten, 1985;Martínez-García et al, 1991;Halpern and Martínez-Marcos, 2003] and from olfactory and associative parts of the pallial amygdala [Lanuza et al, 1997[Lanuza et al, , 1998Novejarque et al, 2004; in birds, this includes at least the arcopallium and the pallial part of nucleus taeniae: Cheng et al, 1999;Kröner and Güntürkün, 1999]; in addition, they project to the sexually dimorphic medial preoptic nucleus [Absil et al, 2002], the paraventricular hypothalamic nucleus, and the ventromedial hypothalamus [Bruce and Neary, 1995a;reviewed by Martínez-García et al, 2002, 2008Medina et al, 2017Medina et al, , 2019. Like in mammals, these avian preoptic/hypothalamic nuclei targeted by EAme have similar functions to those of mammals: the medial preoptic nucleus is involved in male sexual behavior [Panzica et al, 1996[Panzica et al, , 2001aBalthazart et al, 2001;Balthazart and Ball, 2007]; the paraventricular hypothalamic nucleus is an integral part of the hypothalamo-pituitary-glandular axes for control of stress, reproduction, metabolism, and homeostasis, and also regulates the autonomic nervous system by descending projections to the brainstem [De Vries and Panzica, 2006;Kuenzel and Jurkevich, 2010;Smulders, 2021;Grassi et al, 2022]; and the ventromedial hypothalamic nucleus is involved in aspects of sexual behavior and food intake [Kuenzel et al, 1999;Cline et al, 2007;Riters and Pawlisch, 2007]. The EAme of non-avian reptiles also projects to similar preoptic and hypothalamic nuclei involved in neuroendocrine control and social behavior [Martínez-García et al, 2008;O'Connell and Hofm...…”