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      The neurobiology of human allomaternal care; implications for fathering, coparenting, and children's social development

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      Physiology & Behavior
      Elsevier BV

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          Abstract

          Allomothering, the caregiving to offspring by adults other than the biological mother including fathers and other group members, has characterized human societies throughout hominin evolution. Allomothering is common across the animal kingdom and carries long-term fitness benefits to offspring. Guided by our biobehavioral synchrony conceptual frame, we present research from our lab and others addressing the behavioral, hormonal, and neural systems that underpin human allomaternal care by fathers and studies on the coparental bond. Several important aspects of human allomothering are discussed: (i) father-child synchrony, (ii) longitudinal effects of fathering and coparenting on child outcomes (iii) cultural variability in paternal care, (iv) the role of oxytocin, vasopressin, prolactin, and testosterone in the formation and maintenance of human fathering, (v) evolutionary changes in fathers' brains within the parent-offspring interface and their contribution to children's long-term social adaptation, and (vi) the neural correlates of human coparenting. Based on our findings we propose that in the course of hominin evolution fathers' neuroendocrine systems, brain functionality and integrity, and behavioral responses to infant cues have undergone profound natural selection to accommodate the great variability in the paternal role across time and place, culminating in the contemporary cooperative, highly involved coparent observed in modern societies of the developed world.

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          Author and article information

          Journal
          Physiology & Behavior
          Physiology & Behavior
          Elsevier BV
          00319384
          September 2018
          September 2018
          : 193
          : 25-34
          Article
          10.1016/j.physbeh.2017.12.034
          29730038
          a2ec4e69-43b3-4dcb-aac0-a646aa040ab2
          © 2018

          https://www.elsevier.com/tdm/userlicense/1.0/

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