Infanticide and maternal aggression: Synchrony of male and female reproductive strategies in mice

Thirty-six percent of male mice from three strains attacked newborn pups sired by another male. No male attacked its own offspring. Females did not show differential aggression toward males likely (strangers) or unlikely (sires) to attack their pups. Both forms of aggression were unaffected by housing in rooms which did or did not contain the aggression targets. The three strains differed in strength of maternal aggression but not in the incidence of infanticide. Females showed more aggression when mated with males of the same, rather than a different, strain but no differences with intruders of the same or a different strain. Infanticide by males is best viewed as a postcopulatory, intermale-competition strategy, and maternal aggression as a counter strategy.     

Relationship between sexual activity and intraspecific fighting in male mice

Significantly more male mice having cohabited and mated with intact females subsequently displayed intraspecific fighting behavior after castration than males having cohabited with noncycling (ovariectomized) females. Also, intact males that failed to achieve a criterion for aggression during three screening tests subsequently showed a marked increase in fighting after having had copulatory experience relative to males that lived with ovariectomized females. Lastly, spontaneously aggressive males copulated more frequently than nonfighters.     

Female behavior in populations of mice in the presence and absence of male hierarchy

Female aggression may be the regulator of population size in small mammals. Freely growing populations of house mice showed several differences in aggressive female behavior in the presence and the absence of a male hierarchy. Territoriality in females and not in males appeared to maintain social order and regulate population density. Certain females were seen patrolling and guarding the territory and chasing and fighting with both male and female intruders. These females did not fight amongst themselves, suggesting that they were not fighting for rank (as do the males) but for territory. Although these aggressive females produced young, the pups were neglected, and few were weaned. The non-aggressive females were the successful breeders. Aggression by the females only occurred when there was reproduction and increased densities. Assembled females with no males present never show this aggression. The occurrence of “male-type” behavior became most apparent when the males were removed at peak population densities. The removed males were then castrated and injected with testosterone cyprionate. Doses were increased by population cage, and therefore all males returned to each freely growing population were given the same dose. The males given oil placebo injections showed no return of a male hierarchy and the females showed high levels of aggression toward them. Males injected with testosterone cyprionate showed return of male aggression and fighting and mounting of females. But the new “dominant” females continued their patrols and chased males away from their territories and did not permit these males to mount. Male-male fighting consisted primarily of frontal attacks to the face and roll and tumble fights. Female-male aggression consisted primarily of attacks to the posterior region targeted at the base of the tail and the genitals of the male. The males were rarely seen attacking females and then only during mating. Females only attacked each other in defense of their territories.     

Ethopharmacological studies of the effects of β-carbolines and benzodiazepines on murine aggression

The behavioral profiles generated by a benzodiazepine (BDZ) agonist (diazepam), an “inverse” agonist (β-carboline-3-carboxylate ethyl ester, βC-3-CEE), and dihydro-(DHβCs) and tetrahydro-β-carbolines (THβCs) were investigated on aggressive isolated mice using a computerized ethopharmacological technique. Augmentation of intraspecific sociability with a concurrent reduction of aggression are characteristic features of diazepam's effects, whereas βC-3-CEE exerts the opposite effects. βC-3-CEE countered the prosocial activity of diazepam and had intrinsic activities on intraspecific behaviour. Some DHβCs (harmalol and 6-methoxy-harmalan) and THβCs (1-methyl-6-hydroxy-THβC and tetrahydronorharmane) may exacerbate aggression at low (BDZ-negative) doses (1 mg/kg), and inhibit such behavior at higher (serotonin-positive) doses (10-15 mg/kg). The ethological profiles of DHβCs were different from the profiles of THβCs. Differences in ethological profiles of βC-3-CEE, DHβCs, and THβCs seem to reflect the neurochemical (mainly BDZ-and serotonergic) properties of these substances.     

The relationship between aggressive and sexual behavior in male mice: Effects of testosterone and parachlorophenylalanine

The purpose of this study was to clarify the connection between aggressive and sexual behavior with the aid of testosterone propionate (TP) and parachlorophenylalanine (PCPA). Previous studies have indicated that aggressive and sexual behavior are positively correlated, and it has been suggested that both behaviors are related to the level of general arousal. Testosterone has documented effects on both aggressive and sexual behavior. It has been hypothesized that these effects are due to an increased level of general arousal. If this is the case, aggressive and sexual behavior could be restored by administration of drugs excitating the central nervous system, e.g., PCPA. The present study examined the effects of TP and PCPA on aggressive and sexual behavior in gonadectomized male mice. Control animals were injected with sesame seed oil or saline. The level of aggressiveness was assessed by means of dyadic tests with gonad-intact male opponents. For the sexuality tests, a receptive female was placed in the home cage of the experimental male. The results showed that male mice injected with PCPA were more aggressive than the males of the other groups, while the TP-exposed males expressed the most sexual activity. Compared to the control group, the PCPA and TP groups were more active in both the aggression and the sexuality tests. These findings lend support to the hypothesis that the earlier documented correlations between aggressive and sexual behavior could be due to both behaviors being dependent on a certain level of general activation. Aggr. Behav. 24:367–377, 1998. © 1998 Wiley-Liss, Inc.     

The potential effects of protected nests and cage complexity on maternal aggression in house mice

I studied the behavior of nursing house mice (Mus musculus) in captivity and used a two-by-two factorial design to test the hypothesis that the combination of a protected nest along with a chance for the intruders to retreat would improve the ability of resident females to defend their litters from infanticidal males. A chance for the intruder to retreat was manipulated by testing the resident females in either a single- or a two-compartment cage. The effect of a protected nest was examined by providing females with a nest box having a narrow entrance. During each test, an infanticidal adult male was introduced into the cage of a resident female and her pups. I observed that neither the presence of a protected nest nor the chance for the intruders to retreat to a different compartment, or a combination of the two, increased the ability of a female to defend her litter against an intruder male. Moreover, neither of these two factors influenced the overall behavior of the resident females. I obtained similar results after using data from previous studies to examine the influence of both of these factors on the efficiency of maternal aggression. Overall, these two approaches showed that females are often unable to prevent intruders from committing infanticide. I discuss the validity of the hypothesis that maternal aggression evolved as a mechanism to protect offspring from infanticide. Aggr. Behav. 24:385–396, 1998. © 1998 Wiley-Liss, Inc.     

Aversive odors of male mice: Experiential and castration effects,and the predictability of the outcomes of agonistic encounters

The relationship between the aversive urine odors of adult male mice and their agonistic interactions was examined. The urine of 28 isolated intact donors was tested for its aversiveness before the donors had won or lost an agonistic encounter, by spotting a portion of an open field with their urine. Group-housed males (n = 28), each tested with the urine of an ultimate winner and loser, as well as a castrate, avoided both intact types. The urine of castrates was not aversive. Another group of subjects (n = 28), tested with urine collected following the encounter between donors, provided identical results. A second experiment examined the aversiveness of urine from 24 isolate mice, and their responsiveness to urine of other isolates, prior to their encounter. The urine was not highly aversive to the isolates However, winners and losers differed in their responsiveness, as ultimate winners exhibited greater aversion. The results are discussed with regard to territorial maintenance via odors, and how differential responsiveness to odors may influence the outcomes of agonistic encounters.     

Maternal aggression in mice: The non-specific nature of the exteroceptive maintenance by young

Five hours of pup removal during early lactation (Postpartum Day 6) reduced maternal aggression in mice, while placement of the dam's entire litter (six pups) or a single pup behind a double wire mesh partition in the homecage maintained aggression at a level identical to that of mothers in direct contact with their young. When placed behind the partition, unfamiliar 6, 13, and 20-day-old pups, but not 30-day-old mice, maintained the behavior as effectively as the dam's own young. The relationship of the findings to communal rearing conditions in the mouse is discussed.     

Studies on wild house mice VI: Differential effects of the Y chromosome on intermale aggression

The aim of this study is to determine the effects of different parts of the Y chromosome of wild house mice on aggression. To reach this goal, intercrosses were made between two selection lines for attack latency (SAL and LAL) and their congenic strains (SAL. LY and LAL. SY). This procedure resulted in F₁ hybrids that carried the same autosomes, but differed in their X chromosome and the two different parts of their Y chromosomes, the different parts of the Y chromosome being a recombining part called the pseudoautosomal region (PAR) and a non-recombining part (non-PAR). We conclude that both parts of the Y chromosome contribute slightly but significantly to variation in aggression. The major effect is accomplished by the PAR of the aggressive parent; a mirror effect is achieved by the non-PAR of the aggressive parent in interaction with the PAR. © 1994 Wiley-Liss, Inc.     

Antipredator behavior of Swiss-Webster mice in a visible burrow system

Swiss-Webster mice living in a visible burrow system (VBS) reacted to presentation of a live cat in the surface area of the VBS by retreat to the burrows and reductions in nondefensive behaviors such as eating and drinking. Live eat-exposed subjects remained in the burrows 14 hr or more, while subjects exposed to a toy (plush) cat prior to live cat exposure reemerged almost immediately and made many contacts with the toy cat. However, subjects exposed first to the cat and later to a toy cat showed intermediate surface reemergence times and cat contacts during toy cat tests, indicating strong sensitization effects of prior live cat exposure. Previous studies indicated that rats in this situation show retreat to the burrows, surface avoidance, and reduction in nondefensive behaviors. The mouse pattern was similar, with the notable exception that in the first 5min block after cat presentation, mice rapidly alternated retreat to the burrow chambers with reappearance in the tunnel segment near the surface, to scan the surface visually and sniff. Movement during this time block involved a stretch attend posture characteristic also of risk assessment activities in rats. Such visual and olfactory inspection of the cat is not seen in rats in the VBS. This difference may be related to the finding that rats, but not mice, emit ultrasonic “alarm cries” during and after cat exposure. © 1995 Wiley-Liss, Inc.