Internal temporal organisation properly synchronised to the environment is crucial for health maintenance. This organisation is provided at the cellular level by the molecular clock, a macromolecular transcription-based oscillator formed by the clock and the clock-controlled genes that is present in both central and peripheral tissues. In mammals, melanopsin in light-sensitive retinal ganglion cells plays a considerable role in the synchronisation of the circadian timing system to the daily light/dark cycle. Melatonin, a hormone synthesised in the pineal gland exclusively at night and an output of the central clock, has a fundamental role in regulating/timing several physiological functions, including glucose homeostasis, insulin secretion and energy metabolism. As such, metabolism is severely impaired after a reduction in melatonin production. Furthermore, light pollution during the night and shift work schedules can abrogate melatonin synthesis and impair homeostasis. Chronodisruption during pregnancy has deleterious effects on the health of progeny, including metabolic, cardiovascular and cognitive dysfunction. Developmental programming by steroids or steroid-mimetic compounds also produces internal circadian disorganisation that may be a significant factor in the aetiology of fertility disorders such as polycystic ovary syndrome. Thus, both early and late in life, pernicious alterations of the endogenous temporal order by environmental factors can disrupt the homeostatic function of the circadian timing system, leading to pathophysiology and/or disease.Key words: melatonin, circadian, reproduction, clock gene, mouse, rat doi: 10.1111/jne.12144Time as a variable is frequently neglected when we consider the interaction between the organism and the environment. However, life on Earth means that we are under the geophysical cycles that impose approximately 12 h of light and approximately 12 h of dark, the oldest and major environmental time-cue on Earth. Organisms would have faced natural selection in intervals of opportunity and adversity that recur with precise and predictable frequencies, generating an innate temporal programme responsible for circadian oscillations. These are responsible for orchestrating physiology and behaviour and allow organisms to anticipate daily environmental changes (1). The presence of a circadian component in this temporal organisation is also implied in the way that abnormal entraining cycles often impair homeostasis. This can be observed from the simplest and most familiar stress imposed by rapid travel across time zones or, more dramatically, from the high frequency of cardiovascular disease, metabolic syndrome and insomnia observed in workers subjected to night (shift) work schedules (2-4). We begin our discourse with a discussion of the molecular basis for circadian oscillations and how robustly conserved temporal organisation is among organisms. This will lay the framework for a more comprehensive discussion of how chronodisruption impacts the aetiology of disease in our 24/7...