Brown rats and house mice eavesdrop on each other's volatile sex pheromone components.

Mammalian pheromones often linger in the environment and thus are particularly susceptible to interceptive eavesdropping, commonly understood as a one-way dyadic interaction, where prey sense and respond to the scent of a predator. Here, we tested the "counterespionage" hypothesis that predator and prey co-opt each other's pheromone as a cue to locate prey or evade predation. We worked with wild brown rats (predator of mice) and wild house mice (prey of brown rats) as model species, testing their responses to pheromone-baited traps at infested field sites. The treatment trap in each of two trap pairs per replicate received sex attractant pheromone components (including testosterone) of male mice or male rats, whereas corresponding control traps received only testosterone, a pheromone component shared between mouse and rat males. Trap pairs disseminating male rat pheromone components captured 3.05 times fewer mice than trap pairs disseminating male mouse pheromone components, and no female mice were captured in rat pheromone-baited traps, indicating predator aversion. Indiscriminate captures of rats in trap pairs disseminating male rat or male mouse pheromone components, and fewer captures of rats in male mouse pheromone traps than in (testosterone-only) control traps indicate that rats do eavesdrop on the male mouse sex pheromone but do not exploit the information for mouse prey location. The counterespionage hypothesis is supported by trap catch data of both mice and rats but only the mice data are in keeping with our predictions for motive of the counterespionage.

Identification and Field Testing of Volatile Components in the Sex Attractant Pheromone Blend of Female House Mice.

Recently, it was reported (i) that the sex pheromone blend of male house mice, Mus musculus, comprises not only volatile components (3,4-dehydro-exo-brevicomin; 2-sec-butyl-4,5-dihydrothiazole) but also a component of low volatility (the sex steroid testosterone), and (ii) that the sex steroids progesterone and estradiol are sex pheromone components of female house mice. Here we tested the hypothesis that the sex attractant pheromone blend of female mice, analogous to that of male mice, also comprises volatile pheromone components. Analyzing by GC-MS the head space volatiles of bedding soiled with urine and feces of laboratory-kept females and males revealed three candidate pheromone components (CPCs) that were adult female-specific: butyric acid, 2-methyl butyric acid and 4-heptanone. In a two-choice laboratory experiment, adult males spent significantly more time in the treatment chamber baited with both the synthetic steroids (progesterone, estradiol) and the synthetic CPCs than in the paired control chamber baited only with the synthetic steroids. In field experiments, trap boxes baited with both the CPCs and the steroids captured 6.7-times more adult males and 4.7-times more juvenile males than trap boxes baited with the steroids alone. Conversely, trap boxes baited with both the CPCs and the steroids captured 4.3-times more adult males and 2.7-fold fewer adult females than trap boxes baited with the CPCs alone. In combination, these data support the conclusion that butyric acid, 2-methyl butyric acid and 4-heptanone are part of the sex attractant pheromone of female house mice. With progesterone and estradiol being pheromone components of both female brown rats, Rattus norvegicus, and female house mice, these three volatile components could impart specificity to the sexual communication system of house mice, brown rats and possibly other rodent species.

Rhesus macaques (Macaca mulatta) with self-injurious behavior show less behavioral anxiety during the human intruder test.

Self-injurious behavior (SIB) has been linked to anxiety in the human literature, but relatively few studies have explored this link in rhesus macaques. A widely used behavioral assessment of anxiety, the human intruder test (HIT), employs the mildly stressful stimulus of an unfamiliar experimenter to assess anxious behavior in macaques. The HIT was conducted on 59 (20 male) laboratory housed rhesus macaques, 30 with a record of SIB (10 male). If monkeys with SIB have a more anxious phenotype, they should show stronger reactions to the HIT. However, contrary to our predictions, monkeys with SIB did not show higher levels of anxious behavior compared to controls. They spent significantly less time showing anxious behavior and displayed little aggression in response to the stare of the intruder. SIB and control monkeys did not differ in a range score (number of unique behaviors expressed per phase); however, SIB monkeys had a lower change score (total number of behaviors expressed including repetitions) than controls. In general, monkeys that paced regardless of SIB status, showed a reduction in pacing when the intruder entered the room. Possible explanations for the failure of SIB monkeys to show increased anxiety in the HIT include greater exposure of SIB monkeys to unfamiliar humans because of their condition, evidence for a subtype of SIB which is not anxiety related, and/or the presence of comorbid depressive-like symptoms. Am. J. Primatol. 79:e22569, 2017. © 2016 Wiley Periodicals, Inc.