Sociability and gazing toward humans in dogs and wolves: Simple behaviors with broad implications

Sociability, defined as the tendency to approach and interact with unfamiliar people, has been found to modulate some communicative responses in domestic dogs, including gaze behavior toward the human face. The objective of this study was to compare sociability and gaze behavior in pet domestic dogs and in human‐socialized captive wolves in order to identify the relative influence of domestication and learning in the development of the dog–human bond. In Experiment 1, we assessed the approach behavior and social tendencies of dogs and wolves to a familiar and an unfamiliar person. In Experiment 2, we compared the animal's duration of gaze toward a person's face in the presence of food, which the animals could see but not access. Dogs showed higher levels of interspecific sociability than wolves in all conditions, including those where attention was unavailable. In addition, dogs gazed longer at the person's face than wolves in the presence of out‐of‐reach food. The potential contributions of domestication, associative learning, and experiences during ontogeny to prosocial behavior toward humans are discussed.     

An analysis of daily report cards and parent-managed privileges in the improvement of adolescents' classroom performance

A daily report-card system, involving home privileges administered by parents, was developed for use with "problem" junior-high students. In Experiment I, when home privileges and parent praise were contingent on improved school conduct, classwork, daily grades, and teacher satisfaction, the school performance of three students improved considerably. In Experiment II, a similar report-card system was employed with two additional students, except only parent praise was contingent on improved school performance. Under these conditions, one of the students did not bring the report card home, and class performance did not improve until contingent home privileges were added. The school performance of the second student improved with the card and praise alone. However, there appeared to be a slow decline of classwork performance over time. For Experiment III, an instructional manual, describing the report-card program, was written for school guidance counsellors. Two guidance counsellors read the program, used it with one student each, and found that the school performance of both students improved. These results suggest that the daily report-card program with home consequences administered by parents can improve the school performance of, and teacher satisfaction about, students having considerable difficulty in school.     

USING ABERRANT BEHAVIORS AS REINFORCERS FOR AUTISTIC CHILDREN

In a series of experiments, we assessed the efficacy of using autistic children's aberrant behaviors as reinforcers to increase their correct task responding. In Experiment 1, reinforcer conditions of stereotypy, food, and varied (food or stereotypy) were compared. In Experiment 2, the conditions were delayed echolalia, food, and varied (food or delayed echolalia), and in Experiment 3, perseverative behavior was compared with stereotypy and food as potential reinforcers. A multielement design was used for all comparisons, and side-effect measures were recorded during and after teaching sessions as well as at home. Results indicated that, in general, task performance was highest when brief opportunities to engage in aberrant behaviors were provided as reinforcers. Edibles were associated with the lowest performance. Furthermore, no negative side effects (e.g., an increase in aberrant behaviors) occurred. The results are discussed in terms of suggesting a more pragmatic treatment approach by addressing the contingent use of autistic children's aberrant behaviors as reinforcers.     

Verbal contingent stimulation of stuttering in laboratory and home settings

The effect of verbal contingent stimulation for stuttering behaviors was examined during changes of stimulus delivery mode and experimental setting. In Experiment I, contingent stimuli were delivered in the laboratory setting with the experimenter and subject in a face-to-face arrangement versus presentations by the experimenter from a control room via a headset arrangement. In Experiment II, contingent stimulation of stuttering was examined in the laboratory and home setting. Findings revealed that stuttering frequency was reduced in all conditions of both experiments. However, the only significant reductions occurred under the headset delivery conditions in the laboratory setting.     

Are dogs (<Emphasis Type="Italic">Canis familiaris</Emphasis>) misled more by their owners than by strangers in a food choice task?

Dogs are highly skilled in understanding a large variety of human social cues and use them appropriately to solve a number of different cognitive tasks. They rely on human signals even when these are contradictory or misleading and ultimately prevent them from correctly solving a task. In the following two experiments, we investigated whether the owner and a stranger differently influenced dogs’ choices in food discrimination tasks. In Experiment 1, 48 dogs were tested in 3 different conditions: (1) choice between a large and a small amount of dog pellets with no demonstration; (2) choice between a large and a small amount of dog pellets after having witnessed the owner/stranger favouring the small quantity; (3) choice between two single food pellets after observing the owner/stranger choosing one of them. In Experiment 2, 48 dogs could choose between two foods of different palatability: in Condition 1, dogs chose between a slice of sausage and a dry pellet with no demonstration. In Condition 2, the same choice was available but with a person (owner/stranger) showing a preference for the dry pellet. In Condition 3, dogs chose between a single dry pellet and 8 slices of sausage, with the person (owner/stranger) showing a preference for the pellet. In both experiments, dogs conformed to the human’s indications even though these led to the selection of the less advantageous option (i.e. the smaller amount of food in Experiment 1 or the low quality food in Experiment 2). However, the owner and the stranger did not differently influence the dogs’ behaviour. Results show that dogs are willing to follow a person’s indication even when this is visibly (if perhaps only mildly) counterproductive to them and that they are socially prepared to rely equally on cues given by the owner and an unfamiliar friendly person.     

A new perspective on barking in dogs (Canis familiaris)

The disparity in bark frequency and context between dogs (Canis familiaris) and wolves (Canis lupus) has led some researchers to conclude that barking in the domestic dog is nonfunctional. This conclusion attributes the differences primarily to genetic variation caused by domestication rather than to the influence of social environment on ontogeny. Other researchers, however, have concluded that vocal usage and response to vocalizations in mammals are strongly guided by social interactions. Closer evaluation of dog vocalizations with respect to social environment reveals developmental factors that lead to both frequent barking and barking in many contexts. Additionally, spectrographic analysis indicates that bark structure varies predictably with context, suggesting that barks can be divided into contextual subtypes and may be a more complex form of communication than given credit.     

Dog rivalry impacts following behavior in a decision-making task involving food

Dogs learn a great deal from humans and other dogs. Previous studies of socially influenced learning between dogs have typically used a highly trained demonstrator dog who is unfamiliar to the observer. Because of this, it is unknown how dynamics between familiar dogs may influence their likelihood of learning from each other. In this study, we tested dogs living together in two-dog households on whether individual dogs’ rivalry scores were associated with performance on a local enhancement task. Specifically, we wanted to know whether dog rivalry impacted whether an observer dog would approach a plate from which a demonstrator dog had eaten all available food, or whether the observer dog would approach the adjacent plate that still contained food. Dog rivalry scores were calculated using the Canine Behavioral Assessment and Research Questionnaire and indicated each dog’s tendency to engage aggressively with the other household dog. Low-rivalry dogs were more likely to approach the empty plate than high-rivalry dogs when the observer dog was allowed to approach the plates immediately after the demonstrator had moved out of sight. This difference between low- and high-rivalry dogs disappeared, however, when observer dogs had to wait 5 s before approaching the plates. The same pattern was observed during a control condition when a human removed the food from a plate. Compared to low-rivalry dogs, high-rivalry dogs may pay less attention to other dogs due to a low tolerance for having other dogs in close proximity.     

Chimpanzees (Pan troglodytes) do not develop contingent reciprocity in an experimental task

Chimpanzees provide help to unrelated individuals in a broad range of situations. The pattern of helping within pairs suggests that contingent reciprocity may have been an important mechanism in the evolution of altruism in chimpanzees. However, correlational analyses of the cumulative pattern of interactions over time do not demonstrate that helping is contingent upon previous acts of altruism, as required by the theory of reciprocal altruism. Experimental studies provide a controlled approach to examine the importance of contingency in helping interactions. In this study, we evaluated whether chimpanzees would be more likely to provide food to a social partner from their home group if their partner had previously provided food for them. The chimpanzees manipulated a barpull apparatus in which actors could deliver rewards either to themselves and their partners or only to themselves. Our findings indicate that the chimpanzees’ responses were not consistently influenced by the behavior of their partners in previous rounds. Only one of the 11 dyads that we tested demonstrated positive reciprocity. We conclude that contingent reciprocity does not spontaneously arise in experimental settings, despite the fact that patterns of behavior in the field indicate that individuals cooperate preferentially with reciprocating partners.     

Contingent Stimuli Signal Subsequent Reinforcer Ratios

Conditioned reinforcer effects may be due to the stimulus' discriminative rather than its strengthening properties. While this was demonstrated in a frequently‐changing choice procedure, a single attempt to replicate in a relatively static choice environment failed. We contend that this was because the information provided by the stimuli was nonredundant in the frequently‐changing preparation, and redundant in the steady‐state arrangement. In the present experiments, 6 pigeons worked in a steady‐state concurrent schedule procedure with nonredundant informative stimuli (red keylight illuminations). When a response‐contingent red keylight signaled that the next food delivery was more likely on one of the two alternatives, postkeylight choice responding was reliably for that alternative. This effect was enhanced after a history of extended informative red keylight presentation (Experiment 2). These results lend support to recent characterizations of conditioned reinforcer effects as reflective of a discriminative, rather than a reinforcing, property of the stimulus.     

STIMULUS EFFECTS ON LOCAL PREFERENCE: STIMULUS—RESPONSE CONTINGENCIES,STIMULUS—FOOD PAIRING,AND STIMULUS—FOOD CORRELATION

Four pigeons were trained in a procedure in which concurrent‐schedule food ratios changed unpredictably across seven unsignaled components after 10 food deliveries. Additional green‐key stimulus presentations also occurred on the two alternatives, sometimes in the same ratio as the component food ratio, and sometimes in the inverse ratio. In eight experimental conditions, we varied the contingencies surrounding these additional stimuli: In two conditions, stimulus onset and offset were noncontingent; in another two, stimulus onset was noncontingent, and offset was response contingent. In four conditions, both stimulus onset and offset were contingent, and in two of these conditions the stimulus was simultaneously paired with food delivery. Sensitivity to component food ratios was significantly higher when stimulus onset was response contingent compared to when it was noncontingent. Choice changes following food delivery were similar in all eight conditions. Choice changes following stimuli were smaller than those following food, and directionally were completely determined by the food‐ratio:stimulus‐ratio correlation, not by the stimulus contingency nor by whether the stimulus was paired with food or not. These results support the idea that conditional reinforcers may best be viewed as signals for next‐food location rather than as stimuli that have acquired hedonic value, at least when the signals are differential with respect to future conditions.     

Effects of a conditioned reinforcer upon accuracy of match-to-sample behavior in pigeons

Three pigeons were trained to perform a two-key sequential match-to-sample task. During baseline conditions, food reinforcement was contingent upon the first match response to occur following 8-min periods, and orange illumination of both keys preceded the delivery of food by 0.5 sec. The baseline schedule of food reinforcement was in effect throughout the study. In some conditions, a 0.5-sec flash of orange keylight alone was presented contingent upon mismatch responses that followed variable time periods averaging 1 min. Rate of mismatch responses increased and accuracy of matching performances decreased as compared with baseline conditions. The ability of the 0.5-sec orange flash to reinforce mismatch responses was markedly reduced when it no longer immediately preceded the delivery of food.     

SCHEDULE-INDUCED DRINKING: ELICITATION,ANTICIPATION, OR BEHAVIORAL INTERACTION?

We carried out five experiments with rats on fixed-time schedules in order to define the relation between drinking and individual food-pellet presentations. In Experiment 1, unsignaled extra food occurred at the end of occasional fixed intervals, and we compared subsequent drinking patterns with drinking before the extra food presentation. In Experiment 2 we presented signaled and unsignaled extra food and measured elicited and anticipatory drinking patterns. In Experiment 3, we observed the persistence of modified drinking patterns when several consecutive intervals ended with extra pellets. In Experiments 4 and 5, we varied the magnitude of food delivery across (rather than within) sessions to replicate published findings. Results show that schedule-induced drinking is neither elicited by food presentations nor induced by stimuli associated with a high food rate. All subjects seemed to follow a simple rule: during any stimulus signaling an increase in the local probability of food delivery within a session, engage in food-related behavior to the exclusion of drinking. Schedule-induced drinking appears to be the result of dynamic interactions among food-related behavior, drinking, and other motivated behavior, rather than a direct effect of the contingencies of food reinforcement.     

Pointing gestures modulate domestic dogs’ search behavior for hidden objects in a spatial rotation problem

In the spatial domain, domestic dogs are highly inclined to search at the last location where they saw an object disappear and cannot infer that a hidden object has moved imperceptibly from one location to another. In the current study, we examined whether exposure to human social cues modulates dogs’ search behavior for hidden objects. In Experiment 1, twenty dogs were first trained to find an object they saw disappear inside a stationary container in the presence (social group) or absence (non-social group) of pointing gestures. In tests, the containers were rotated 180° around a central axis. The dogs in the non-social group systematically searched at the initial (now incorrect) hiding location, whereas the dogs in the social group chose correctly significantly above chance. In Experiment 2, we tested whether pre-exposure to human pointing has an impact on dogs’ use of gestures. No gestures were given during training and both the social and non-social conditions were administered to each of the ten dogs. In contrast to Experiment 1, the performance of dogs in the social condition dropped significantly and varied substantially from one dog to another. Overall, this study suggests that dogs’ tendency to use human signals is so strong that it even outweighs their spatial bias to search where they saw an object disappear; however, this penchant to use human gestures appears to be dependent on the degree of familiarity of the dog with these signals.     

How does dominance rank status affect individual and social learning performance in the dog (<Emphasis Type="Italic">Canis familiaris</Emphasis>)?

Dogs can learn effectively to detour around a V-shaped fence after observing a demonstration from either an unfamiliar human or dog demonstrator. We found earlier that there is substantial individual variation between the dogs’ performance, even when using the same experimental conditions. Here, we investigate if the subjects’ relative dominance rank with other dogs had an effect on their social learning performance. On the basis of the owners’ answers to a questionnaire, subjects from multi-dog homes were sorted into groups of dominant and subordinate dogs. In Experiment 1, dominant and subordinate dogs were tested without demonstration and we did not find any difference between the groups—they had similarly low detour performances on their own. In Experiment 2 and 3, dogs from single dog and multi-dog households were tested in the detour task with demonstration by an unfamiliar dog, or human, respectively. The results showed that social learning performance of the single dogs fell between the dominant and subordinate multi-dogs with both dog and human demonstration. Subordinate dogs displayed significantly better performance after having observed a dog demonstrator in comparison to dominant dogs. In contrast, the performance of dominant and subordinate dogs was almost similar, when they observed a human demonstrator. These results suggest that perceived dominance rank in its own group has a strong effect on social learning in dogs, but this effect seems to depend also on the demonstrator species. This finding reveals an intricate organization of the social structure in multi-dog households, which can contribute to individual differences existing among dogs.     

Operant conditioning of autogrooming in vervet monkeys: Cercopithecus aethiops

Vervet monkeys received food reinforcement contingent on autogrooming. Experiment 1 reinforced grooming on a schedule of increasing intermittency and grooming increased in frequency and duration; with only pauses reinforced, grooming decreased in frequency and duration. Experiment 2 demonstrated differentiation of operant autogrooming; in each session a different single form of grooming was reinforced (for example, grooming the tail only), and that form increased in frequency while other forms became less frequent. In Experiment 3 scratching was succesfully conditioned with a method that selectively reinforced variety in behavior; reinforcement was contingent on a shift in scratching form. In Experiment 4, with no contingencies on grooming, a prefood stimulus did not increase autogrooming whether or not grooming had previously resulted in contingent reinforcement. The form of conditioned autogrooming resembled the form of unconditioned autogrooming. The discussion suggests how reinforcement principles can account for changes in the topography of operant behavior.     

Food delivery as a conditional stimulus: Feature-learning and memory in pigeons

Three experiments investigated the learning and memory of discriminations based on presence versus absence of a pre-trial food delivery. In Experiment 1 half the illuminations of a response key were followed by food regardless of the subject's behavior. In one group an extra food delivery preceded only reinforced trials (feature-positive condition), whereas in a second group it preceded only nonreinforced trials (feature-negative condition). Key pecks and approaches revealed more rapid and superior discrimination learning in the first group. Experiment 2 replicated the results of Experiment 1 but yielded no evidence that greater “unexpectedness” of pretrial food conditions facilitates discriminative performance. In Experiment 3, individual pigeons trained on a conditional discrimination exhibited a within-subject feature-positive superiority. Delay between pretrial and trial stimuli interacted with feature-positive versus feature-negative training in both the between-group (Experiment 2) and within-subject (Experiment 3) procedures: performance was decremented at both short and long delays in the feature-positive condition but was decremented only at longer delays in the feature-negative condition. The feature-positive superiority obtained here is incompatible with explanations based on either the general concept of “perceptual organization” or on the conditional nature of feature-negative discriminations.     

Beyond the distributional input? A developmental investigation of asymmetry in infants’ categorization of cats and dogs

Two experiments are reported using a visual familiarization categorization procedure. In both experiments, infants were familiarized with sets of stimuli previously shown to contain asymmetric feature distributions that support an asymmetry in young infants' categorization of cats and dogs (i.e. infants' cat category excludes dogs but their dog category includes cats). In Experiment 1, the asymmetry was replicated in 4-month-old infants. In contrast, 10-month-old infants demonstrated exclusive category representations for both cats and dogs. In Experiment 2, an additional group of 10-month-olds demonstrated exclusive representations for both cats and dogs under conditions of very limited within-task category familiarization. Potential mechanisms underlying the shift from an asymmetric to a symmetric pattern of categorization in the first year are discussed.     

Interactions between the effects of food and water motivating operations on food‐ and water‐reinforced responding in mice

Two experiments examined interactions between the effects of food and water motivating operations (MOs) on the food‐ and water‐reinforced operant behavior of mice. In Experiment 1, mice responded for sucrose pellets and then water reinforcement under four different MOs: food deprivation, water deprivation, concurrent food and water deprivation, and no deprivation. The most responding for pellets occurred under food deprivation and the most responding for water occurred under water deprivation. Concurrent food and water deprivation decreased responding for both reinforcers. Nevertheless, water deprivation alone increased pellet‐reinforced responding and food deprivation alone likewise increased water‐reinforced responding relative to no deprivation. Experiment 2 demonstrated that presession food during concurrent food and water deprivation increased in‐session responding for water relative to sessions where no presession food was provided. Conversely, presession water during concurrent food and water deprivation did not increase in‐session responding for pellets. These results suggest that a) the reinforcing value of a single stimulus can be affected by multiple MOs, b) a single MO can affect the reinforcing value of multiple stimuli, and c) reinforcing events can also function as MOs. We consider implications for theory and practice and suggest strategies for further basic research on MOs.     

Contingency effects with maintained instrumental reinforcement

In three experiments we investigated the effect on the performance of thirsty rats of varying the instrumental contingency between lever pressing and the delivery of a saccharin reinforcer. In Experiment 1, the subjects performed more slowly in a non-contingent condition, in which the momentary probability of reinforcement was unaffected by whether or not the animals pressed, than in a contingent condition in which the reinforcer was never presented except following a lever press. This was true of performance under both random ratio and interval schedules in which the function determining the probability of reinforcement following a lever press remained the same across the contingent and non-contingent conditions. Experiment 2 demonstrated that instrumental performance was less affected when the contingency was degraded by the introduction of free reinforcers if these reinforcers were signalled. In Experiment 3, lever pressing was reinstated to some degree after non-contingent training by giving non-reinforced exposure to the operant chamber in the absence of the lever. These results suggest that free reinforcers depress instrumental behaviour through a performance mechanism engaged by their ability to support conditioning of the contextual cues.     

SUPPRESSIVE AND FACILITATIVE EFFECTS OF SHOCK INTENSITY AND INTERRESPONSE TIMES FOLLOWED BY SHOCK

Although response‐dependent shock often suppresses responding, response facilitation can occur. In two experiments, we examined the suppressive and facilitative effects of shock by manipulating shock intensity and the interresponse times that produced shock. Rats' lever presses were reinforced on a variable‐interval 40‐s schedule of food presentation. Shock followed either long or short interresponse times. Shock intensity was raised from 0.05 mA to 0.4 mA or 0.8 mA. Overall, shock contingent on long interresponse times punished long interresponse times and increased response rates. Shock contingent on short interresponse times punished short interresponse times and decreased response rates. In Experiment 1, raising the range of interresponse times that produced shock enhanced these effects. In Experiment 2, the effects of shock intensity depended on the interresponse times that produced shock. When long interresponse times produced shock, low intensities increased response rates. High intensities decreased response rates. When short interresponse times produced shock, high shock intensities punished short interresponse times and decreased response rates more than low intensities. The results may explain why punishment procedures occasionally facilitate responding and establish parameters for future studies of punishment.