Abstract

Twilight is characterised by changes in both quantity (“irradiance”) and quality (“colour”) of light. Animals use the variation in irradiance to adjust their internal circadian clocks, aligning their behaviour and physiology with the solar cycle. However, it is currently unknown whether changes in colour also contribute to this entrainment process. Using environmental measurements, we show here that mammalian blue–yellow colour discrimination provides a more reliable method of tracking twilight progression than simply measuring irradiance. We next use electrophysiological recordings to demonstrate that neurons in the mouse suprachiasmatic circadian clock display the cone-dependent spectral opponency required to make use of this information. Thus, our data show that some clock neurons are highly sensitive to changes in spectral composition occurring over twilight and that this input dictates their response to changes in irradiance. Finally, using mice housed under photoperiods with simulated dawn/dusk transitions, we confirm that spectral changes occurring during twilight are required for appropriate circadian alignment under natural conditions. Together, these data reveal a new sensory mechanism for telling time of day that would be available to any mammalian species capable of chromatic vision.

Highlights

  • The ability to predict and adapt to recurring events in the environment is fundamental to survival

  • Assessing external time is typically thought to rely on measuring large changes in ambient light intensity that occur over dawn/dusk

  • We show that the mammalian blue–yellow colour discrimination axis provides a more reliable indication of twilight progression than a system solely measuring changes in light intensity

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Summary

Introduction

The ability to predict and adapt to recurring events in the environment is fundamental to survival. Organisms across the living world achieve this using endogenous circadian clocks [1,2,3]. If such clocks are to fulfil their ethological function they need to be regularly reset to local time. This is achieved by sensory inputs that report changes in the physical environment providing a useful proxy for time of day. By far the best characterised of these input pathways is that recording the diurnal change in the overall quantity of light reaching the earth’s surface (irradiance). In the case of mammals, a dedicated retino-hypothalamic projection brings this visual information to the brain’s “master” clock in the suprachiasmatic nuclei (SCN) [4,5,6,7]

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