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Rands, S. A.

Publications and source records attributed to Rands, S. A..

3 recordsLinked to original sources

Red deer Cervus elaphus blink more in larger groups

Most animals need to spend time being vigilant for predators, at the expense of other activities such as foraging. Group-living animals can benefit from the shared vigilance effort of other group members, with individuals reducing personal vigilance effort as group size increases. Behaviours like active scanning or head lifting are usually used to quantify vigilance, but may not be accurate measures as the individual could be conducting them for other purposes. We suggest that measuring an animals blinking rate gives a meaningful measure of vigilance: increased blinking implies reduced vigilance, as the animal cannot detect predators when its eyes are closed. We demonstrate that as group size increases in red deer, individuals increase their blink rate, confirming the prediction that vigilance should decrease. Blinking is a simple non-invasive measure, and offers a useful metric for assessing the welfare of animals experiencing an increase in perceived predation risk or other stressors.

animal behavior and cognition

The neonicotinoid insecticide imidacloprid disrupts bumblebee foraging rhythms and sleep

Neonicotinoids have been implicated in the large declines observed in flying insects such as bumblebees, an important group of pollinators[1]. Neonicotinoids are agonists of nicotinic acetylcholine receptors that are found throughout the insect central nervous system, and are the main mediators of synaptic neurotransmission[2]. These receptors are important for the function of the insect central clock and circadian rhythms[3, 4]. The clock allows pollinators to coincide their activity with the availability of floral resources, favourable flight temperatures, as well as impacting learning, navigation and communication[5]. Here we show that exposure to the field relevant concentration of 10 {micro}g/L of imidacloprid can cause a reduction in foraging activity and reduce both locomotor and foraging rhythmicity in Bombus terrestris. Foragers showed an increase in daytime sleep and an increase in the proportion of activity occurring at night. This would likely negatively impact foraging and pollination opportunities, reducing the ability of the colony to grow and reproduce, endangering crop yields.

pharmacology and toxicology

Neonicotinoids disrupt memory, circadian behaviour and sleep

Globally, neonicotinoids are still the most used insecticides, despite their well-documented sub-lethal effects on beneficial insects1. Neonicotinoids are agonists at the nicotinic acetylcholine receptors, the main mediator of synaptic transmission in the insect brain2-5, making them highly potent neurotoxins and insecticides6,7. Memory, circadian rhythmicity and sleep are essential for efficient foraging in many pollinating insects, and involve nicotinic acetylcholine receptor signalling2,4,8-10. The effect of field-relevant concentrations of European Union-banned neonicotinoids: imidacloprid, clothianidin and thiamethoxam, as well as the currently unbanned thiacloprid were tested on Drosophila memory, circadian rhythms and sleep. Field-relevant concentrations of imidacloprid, clothianidin and thiamethoxam disrupted learning, behavioural rhythmicity and sleep whilst thiacloprid exposure only affected sleep. Exposure to imidacloprid and clothianidin directly affected neurophysiology, preventing the day/night remodelling and accumulation of pigment dispersing factor neuropeptide in the dorsal terminals of clock neurons. Knockdown of the neonicotinoid susceptible D1 and D{beta}2 nicotinic acetylcholine receptor subunits in the mushroom bodies or clock neurons recapitulated the neonicotinoid like deficits in memory or circadian/sleep behaviour demonstrating that neonicotinoid effects are likely mediated in the mushroom body and clock circuitry. Disruption to learning, circadian rhythmicity and sleep are likely to have far-reaching detrimental effects on beneficial insects in the field.

pharmacology and toxicology