Ontogeny of sex differences in defensive burying behavior in rats: effect of social isolation

The aim of the present experiments was to clarify sex differences in socio-developmental factors that affected defense behavior in rats. Sex differences in the defensive burying behavior of rats, and related social factors, were explored in three developmental stages: juvenile, puberty, and adult; 30, 50, and 80 days of age, respectively. The duration of burying, digging into bedding material, stretch-attend postures, and crouch/freezing were measured in a shock-prod test. For males, the duration of burying was longer in the juvenile and pubertal stages than in adulthood. For females, no age differences in the duration of burying were found. Males showed longer burying durations than females in both the juvenile and pubertal stages. For both sexes, the highest duration of digging was found in the juvenile stage, and females showed longer durations of digging than males. Both male and female rats isolated during the juvenile stage, from 26 to 40 days of age, showed smaller durations of burying behavior compared to pair-reared rats. This effect of juvenile isolation was maintained among both adult males and females even when they were returned to pair rearing after isolation. Isolation during adulthood, from 66 to 80 days of age, increased burying behavior in males, but decreased it in females. The durations of digging, stretch-attend postures, and crouch/freezing were not affected by isolation. The decrease in defensive burying and its increase resulting from isolation in adult male rats, suggest that the emergence of adult-like social relationships in males suppressed the duration of burying. Male and female rats isolated during the juvenile stage maintained lower levels of burying, suggesting that social experience as juveniles is important for the emergence of defensive burying behavior.     

Factors in the waning of muricide in the rat: I. Analysis of intra- and intersession decrement

If each mouse killed by a rat is removed from the rat's home cage and replaced immediately by another live mouse, the rate of killing declines within 1- and 3-hr sessions. Muricide could not then be dishabituated by either a “nonspecific” stimulus (a loud noise) or a specific change in target characteristics (a frog substituted for the mouse). By systematically varying intersession intervals, we found that 1 hr of ad lib killing produced a monotonically decreasing suppression of muricide over the succeeding 96 hr. Subjects performed an interesting kind of forward didng which was influenced by both dishabituating stimuli and killing; this may be a form of die placement behavior.     

Rat defensive behavior: burying noxious food.

In Experiment 1, rats living in chambers containing bedding material were injected with a toxicosis-producing dose of lithium chloride shortly after their initial taste of sweetened condensed milk. They consumed no additional milk and used the bedding to bury the spout through which the milk had been delivered, although they did not bury a concurrently available water spout. In another control condition, rats did not bury a spout containing a novel solution (saccharin) not paired with toxicosis. In Experiment 2, rats did not bury a milk spout until milk consumption was followed by toxicosis. In Experiment 3, rats buried a spout containing Tabasco pepper sauce but not a concurrently available water spout. Thus, burying the food source appears to be an integral component of the rat's defensive reaction to noxious food.     

Stimulus control of defensive burying in the rat

Rats shocked once through a wire-wrapped stationary prod mounted on the wall of a test chamber incorporated the bedding material covering the chamber floor into a defensive reaction. When tested 1 min later, they approached the prod and buried it. Evidence was provided by three separate studies of this burying response that rats had learned about the association of both the position and brightness of the prod with shock after this single conditioning trial. In Experiment 1, the amount of burying decreased if either the position or brightness of the prod had been changed prior to the test. In Experiments 2 and 3, rats were shocked through one of two prods (white or black) mounted on opposite walls of the test chamber. When the positions of the prods were unchanged for the test, almost every subject buried the prod through which it had been shocked, even when the conditioning-test interval was 24 hr; whereas, each rat directed substantial amounts of bedding material at both prods when the positions of the two prods were reversed. Thus, discriminated “avoidance” learning can be rapid, reliable, and enduring when shock is administered “by” a clearly defined stimulus object, i.e., when cue and consequence are spatially contiguous.     

Chronic exposure to a novel odor increases pups' vocalizations, maternal care, and alters dopaminergic functioning in developing mice

This study was designed to assess the stress effect of manipulation of the olfactory environment in developing mice. In a first experiment it was found that mouse pups could be stressed (as measured by an increase in ultrasonic calls) by removing the litter from the dam for 15 min/day for the first 14 days of life and exposing them to a novel odor (clean bedding). This stress procedure also produced a long-term modification in maternal behavior. The stress response (ultrasounds) and the modification of maternal behavior were prevented by providing the litter with home cage bedding during maternal separation. In a second experiment it was demonstrated that early stress influenced apomorphine-induced wall climbing behavior in 15-day-old mice, suggesting stress-induced alterations in the dopaminergic system. Pups exposed to clean bedding during infancy exhibited more wall climbing behavior than pups never separated from the mother. Moreover, preventing the early stress response during mother-offspring separation, by providing pups with home cage bedding, eliminated the increase in apomorphine-induced wall climbing. Taken together these results suggest that olfactory cues are decisive in characterizing stressful situations inducing both immediate and long-lasting effects in mouse pups.     

Conditioned and unconditioned defensive burying in the rat

When rats first encountered a mouse-trap or a flashbulb in a chamber to which they had been habituated, they buried it with bedding material from the floor of the chamber, whereas rats previously habituated to the trap or the flashbulb did not. Conversely, rats did not bury a stationary, wire-wrapped wooden prod or a length of polyethylene tubing, even on first encounter. However, almost every rat struck by the trap, shocked by the prod, exposed to an airblast from the tube, or to a flash of the bulb, buried the respective source of aversive stimulation with the bedding material, even when a comparable control object was present during conditioning and testing. Thus, the phenomenon of defensive burying is not restricted to situations in which neutral objects serve as the source of painful electric shock. Rats seem to enter the experimental environment with an already established tendency to bury some objects (unconditioned defensive burying) but not others, and they readily learn to selectively bury an object that has been the source of any one of a variety of aversive stimuli (conditioned defensive burying).     

Effects of home nest odors on black-white preference in the developing rat: implications for developmental learning research

Developing animals 17 and 30 days of age were tested for black-white preference in the presence of either clean shavings or soiled bedding material from the home cage. Home nest shavings markedly reduced dark preference in 17-day-old rats but had no effect on dark preference in 30-day-old rats. Because many developmental studies have used two-compartment, black and white chambers to study the effects of familiar home nest shavings on learning and memory, it may be that differential preference for black influenced the results obtained. The apparent alleviation of learning and memory deficits produced by the presence of home nest shavings may have been the result of changes in black-white preference rather than differences in learning and memory per se. Similar influences may underlie the effects of home nest stimuli on other learning tasks such as spatial alternation.     

Development of defensive burying in Rattus norvegicus: experience and defensive responses

Rats (Rattus norvegicus) deprived of the opportunity to interact with particulate matter until they were young adults engaged in defensive burying after they were shocked by a wire-wrapped dowel in a test chamber that held bedding material. Interacting with a particulate substrate during development is not necessary for the expression of defensive burying in adulthood. However, interacting with a particulate substrate early in the rats' lives did have a substantial effect on the emergence and maintenance of burying behavior. Defensive burying developed at a later age and declined at an earlier age in rats maintained on wire mesh from birth until testing than it did in rats raised until weaning on bedding and housed on mesh thereafter. Because defensive burying is a complex, flexible, yet reliable response sequence that cannot be performed without the appropriate substrate, it has considerable potential as a model for the study of the development of species-specific defense responses.     

Sexual reinforcement in the female rat.

Sexual reinforcement in the female rat was studied in a preparation that allowed continuous operant responding for access to a male rat leading to intromission. Experiment 1 used a high operant level nose-poke response to test the possible reinforcing effects of some components of access to a male. A simple tone stimulus used as a conditioned reinforcer and two odor stimuli, target male bedding and emulsified preputial gland, were tested. None of these contingent events altered responding above or below operant level. Access to the male, which was always accompanied by intromission, immediately increased response rate when it was made contingent upon the nose-poke response. Performance on fixed-ratio schedules was erratic, and response rate was low in comparison to typical food-reinforced responding. An interresponse-time analysis indicated, however, that some effect of the ratio contingency may have been present. In Experiment 2, several modifications of the procedure were tested with the objective of creating a more tractable preparation for behavior analysis. Response type and the hormone delivery method were changed, and 2 target males were used instead of 1. The latter tripled the average number of reinforcers earned in a single session. Differences between sexual and other reinforcers are discussed in terms of procedural, quantitative, and motivational aspects of the sexual reinforcement procedure.     

Social olfaction in male brown lemmings (Lemmus sibiricus = trimucronatus) and collared lemmings (Dicrostonyx groenlandicus): II. Discrimination of mated and unmated females

When tested in a Y-maze olfactometer, male brown and collared lemmings (Lemmus sibiricus = trimucronatus and Dicrostonyx groenlandicus) preferred the odor of unmated receptive females to the odor of females with which they had just copulated. Similarly, sexually satiated males preferred the odor of an unmated receptive female to that of a strange female that had recently copulated with another male. Sexually experienced males without recent copulatory experience also demonstrated this preference, but sexually naive males did not. Sexually satiated collared lemmings preferred the odor of bedding from a novel estrous female to bedding from the female with which they had just copulated even when the bedding was collected before mating occurred. These results suggest that discrimination between prior mates and unmated females may be based on individual recognition as well as recognition of subclasses of females (i.e., mated vs. unmated, familiar vs. unfamiliar).     

Evidence for a time constant in rate of speech under delayed auditory feedback

This experiment investigates an apparent discrepancy in experimental measurements of the effect of texture predictability upon reading disruption under delayed auditory feedback (DAF). By measuring relative DAF decrement in three different ways, it is shown that the previous findings can be related; Fillenbaum's hypothesis of increased disruption by DAF with an increase in predictability of the material is rejected, less disruption being obtained after practice on a particular passage. Almost identical ratios of DAF rate divided by normal rate are found irrespective of the type of reading material and stage in practice. This has not been reported previously and suggests that behaviour under DAF may be related to behaviour under normal conditions by a multiplicative constant. These results are also consistent with the notion of limited channel capacity and the partitioning of attention between two sources of information.     

Genetic influences on digging behaviors in mice (Mus musculus) in laboratory and seminatural settings

Digging behaviors of several inbred strains of laboratory mice and some of their crosses were examined in three contexts. In laboratory burrow boxes, C57BL/6Abg mice constructed more sophisticated burrow systems than did BALB/cAbg mice. Their F1 hybrids built burrow systems more complex than either parental strain. The same pattern of genetic influence was observed in an outdoor pen. In an escape task that required digging, BALB/c mice escaped more quickly than did C57BL/6 mice; their F1 hybrids showed dominance toward the BALB/c phenotype. These results indicate that behavioral polymorphisms in digging behavior, which may relate to habitat selection, have a genetic basis. The dominance and overdominance toward the better digging parental strain in each type of task suggest the possible evolutionary importance of these digging behaviors.     

Behavioral correlates of learned aggression in male mice

The aims of this paper are to study the aggressive behavior in male mice with consecutive experience of victories in 2, 10, and 20 days (T2, T10, and T20 winners) of daily agonistic confrontations under the sensory contact model and to determine the most probable behavioral domains that should be used as animal models for learned aggression in humans. It has been shown that the structure of winners' behavior changes from test to test: the attacking behavior prevailed (81% of the total time) in the behavior of T2 winners. Attacks and diggings (herein: digging up and scattering the litter on the partner' territory) prevailed in the behavior of T10 winners (each approximately 40%). T20 winners demonstrated aggressive grooming half of the testing time and digging behavior 25% of the time. Correlational analysis revealed that the number of significant correlations between the behavioral domains (attacking, digging, aggressive grooming, self‐grooming, threats, rotations) and between different behavioral parameters (latency, number, total and average time) of one behavioral domain are growing from the second test to twentieth test, and the relationships between the behavioral domains change qualitatively. The following may be regarded as elements of learned aggression in male mice: (1) appearance of aggressive grooming instead of the intensive attacking behavior and (2) involvement of the digging behavior in the hostile behavior together with the threats and attacking behavior. Negative correlations between parameters of the behavioral domains may testify to the replacement of one behavioral pattern by another and reflect learned behavior. Positive correlations between certain behavioral domains may reflect the formation of a common motivational background for the winners' behavior. Aggr. Behav. 26:386–400, 2000. © 2000 Wiley‐Liss, Inc.     

Combat-Related Killing: Expanding Evidence-Based Treatments for PTSD

Despite its prevalence, killing in war is an experience that may not fit neatly into existing models of posttraumatic stress disorder (PTSD) and its treatment. The context in which killing occurred may be complex. Furthermore, while killing may certainly be fear based, an individual may have also killed in response to losing someone close and experiencing sadness and anger, as opposed to fear. While evidence-based treatments for PTSD may be a good starting point for killing-related trauma, we argue that existing treatments need to be expanded. Complex killing-related cognitions that may not be anticipated or identified, moral injury, self-forgiveness, and loss are all important issues that arise that may need to be addressed in greater detail. Consequently, we have developed a 6- to 8-session individual treatment module for those impacted by killing in war, expressly designed for use with existing evidence-based treatments for PTSD, currently being validated for use in clinical practice. We see this module as supplementary, rather than as a replacement, building on the skills that veterans have already learned within these treatments. By expanding the types of treatments we offer those who have killed in war, we can ensure that we are providing veterans with comprehensive treatment that takes the complexities of war and its aftermath into account.     

Pharmacological antagonism of mouse-killing behavior in the olfactory bulb lesion-induced killer rat

Representative agents from all of the major classes of drugs that have been reported to be selective antagonists of spontaneous mouse-killing behavior (i.e., antidepres-sants, antihistamines, anticholinergics, and stimulants) were tested for their ability to antagonize the mouse-killing response in rats that became killers following removal of the olfactory bulbs (O.B. lesion-induced killer rat) and in spontaneous killers. All of the drugs tested selectively antagonized the killing behavior of both spontaneous and lesion-induced mouse-killing rats. Several drugs (i.e., imipramine, amitriptyline, d-amphetamine, and chlorpheniramine) were found to be significantly less potent antagonists of mouse killing in the 0.6. lesioned rat as compared to spontaneous killers. Since all of the drugs that exhibited significant differences in activity between the two models have been shown to possess the ability to elevate norepinephrine levels at receptor sites in the brain, alterations in noradrenergic systems may account for the differences in sensitivity that were observed in this study. The possibility that there may be a common neural substrate for mouse killing in the two models is discussed.     

Housing pregnant mice (Mus musculus) in small groups facilitates the development of odor-based homing in offspring

Infant mice (Mus musculus) born to dams housed in isolation throughout pregnancy (IsoPreg) begin differentially approaching homenest bedding over clean bedding on Postnatal Day 6. Offspring of dams housed with 2 other potentially pregnant conspecifics (SocPreg) display such homing behavior on Day 4. Earlier onset of homing reflects facilitated olfactory responsiveness in SocPreg pups, rather than qualitative or quantitative differences in IsoPreg versus SocPreg nest odors, body growth, or motoric capabilities. Exposing pregnant IsoPreg dams to SocPreg bedding also accelerated homing onset in the offspring, though not to the same extent as the full social context. Thus, it appears that the facilitation of homing is mediated through the pregnant dam by a combination of chemical cues and other social stimuli.     

Conditions necessary for sand digging in laboratory rats

Continuous availability of a sand blocked tube elicited intense and persistent digging by laboratory rats. Neither training nor prior exposure to the apparatus were necessary for response initiation. Continuous presence of an open pile of sand would not elicit digging. No theoretical explanation is offered.     

Evidence that Killing Escalates Within‐Subjects in a Bug‐Killing Paradigm

Prior research has examined killing behavior using a paradigm in which participants believe (falsely) that they are killing bugs. This work suggests that killing behavior escalates. In the present study, we sought to replicate the basic escalation effect within‐subjects. Further, in doing so, we controlled for experimenter “sanctioning” of killing that may have differed with key between‐subjects manipulations in the prior research. To control for this possible confound, the present experiment held experimenter instructions constant and examined whether killing naturally escalated within‐subjects across two 12‐sec bug‐killing tasks. Additionally, to verify that escalation is due to killing per se and not just physical practice of the procedure, we manipulated whether the procedure was described as real killing or simulated killing. Results showed that when participants thought they were killing bugs, the number of bugs put into the grinder increased from the first to the second killing task. No such escalation occurred when participants performed the procedure while knowing the killing was simulated. Thus, killing of bugs escalates and is not simply a consequence of perceived sanctioning of killing by an experimenter or simulated practice of the procedure.     

Assisted death and martyrdom.

Against the backdrop of ancient, mediaeval and modern Catholic teaching prohibiting killing (the rule against killing), the question of assisted suicide and euthanasia is examined. In the past the Church has modified its initial repugnance for killing by developing specific guidelines for permitting killing under strict conditions. This took place with respect to capital punishment and a just war, for example. One wonders why in the least objectionable instance, when a person is already dying, suffering, and repeatedly requesting assistance in dying, there is still such widespread condemnation of assisted suicide and euthanasia. In a Gedankexperiment, I suggest that certain stories of martyrdom in the history of the Christian Church shed some light on the role of taking one's life, or putting one's life in danger out of love. I further suggest that requesting assisted suicide and/or euthanasia from the motive of love of one's family or care givers might possibly qualify as one instance of justifiable euthanasia, although I acknowledge that the Church will not be making changes in its stance any time soon.