9 research outputs found
Dogs’ expectation about the signalers’ body size by virtue of their growls
Several studies suggest that dogs, as well as primates, utilize a mental representation of the signaler after hearing its vocalization and can match this representation with other features provided by the visual modality. Recently it was found that a dogs' growl is context specific and contains information about the caller's body size. Whether dogs can use the encoded information is as yet unclear. In this experiment, we tested whether dogs can assess the size of another dog if they hear an agonistic growl paired with simultaneous video projection of two dog pictures. One of them matched the size of the growling dog, while the other one was either 30% larger or smaller. In control groups, noise, cat pictures or projections of geometric shapes (triangles) were used. The results showed that dogs look sooner and longer at the dog picture matching the size of the caller. No such preference was found with any of the control stimuli, suggesting that dogs have a mental representation of the caller when hearing its vocalization
Why do dogs (Canis familiaris) select the empty container in an observational learning task?
Many argue that dogs show unique susceptibility to human communicative signals that make them suitable for being engaged in complex co-operation with humans. It has also been revealed that socially provided information is particularly effective in influencing the behaviour of dogs even when the human’s action demonstration conveys inefficient or mistaken solution of task. It is unclear, however, how the communicative nature of the demonstration context and the presence of the human demonstrator affect the dogs’ object-choice behaviour in observational learning situations. In order to unfold the effects of these factors, 76 adult pet dogs could observe a communicative or a non-communicative demonstration in which the human retrieved a tennis ball from under an opaque container while manipulating another distant and obviously empty (transparent) one. Subjects were then allowed to choose either in the presence of the demonstrator or after she left the room. Results showed a significant main effect of the demonstration context (presence or absence of the human’s communicative signals), and we also found some evidence for the response-modifying effect of the presence of the human demonstrator during the dogs’ choice. That is, dogs predominantly chose the baited container, but if the demonstration context was communicative and the human was present during the dogs’ choice, subjects’ tendency to select the baited container has been reduced. In agreement with the studies showing sensitivity to human’s communicative signals in dogs, these findings point to a special form of social influence in observational learning situations when it comes to learning about causally opaque and less efficient (compared to what comes natural to the dog) action demonstrations
Does the A-not-B error in adult pet dogs indicate sensitivity to human communication?
Recent dog-infant comparisons have indicated that the experimenter's communicative signals in object hide-and-search tasks increase the probability of perseverative (A-not-B) errors in both species (Topál et al. 2009). These behaviourally similar results, however, might reflect different mechanisms in dogs and in children. Similar errors may occur if the motor response of retrieving the object during the A trials cannot be inhibited in the B trials or if the experimenter's movements and signals toward the A hiding place in the B trials ('sham-baiting') distract the dogs' attention. In order to test these hypotheses, we tested dogs similarly to Topál et al. (2009) but eliminated the motor search in the A trials and 'sham-baiting' in the B trials. We found that neither an inability to inhibit previously rewarded motor response nor insufficiencies in their working memory and/or attention skills can explain dogs' erroneous choices. Further, we replicated the finding that dogs have a strong tendency to commit the A-not-B error after ostensive-communicative hiding and demonstrated the crucial effect of socio-communicative cues as the A-not-B error diminishes when location B is ostensively enhanced. These findings further support the hypothesis that the dogs' A-not-B error may reflect a special sensitivity to human communicative cues. Such object-hiding and search tasks provide a typical case for how susceptibility to human social signals could (mis)lead domestic dogs
The effect of development and individual differences in pointing comprehension of dogs
In spite of the rather diVerent procedures actually
used in comparative studies to test the ability of diVerent
species to rely on the human pointing gesture, there is
no debate on the high performance of dogs in such tasks.
Very little is known, however, on the course through which
they acquire this ability or the probable factors inXuencing
the process. Important developmental questions have
remained unsolved and also some methodological concerns
should be addressed before we can convincingly argue for
one interpretation or another. In this study we tested 180
dogs of diVerent age (from 2 months to adults) to investigate
their performance in the human distal momentary
pointing gesture. The results, analyzed at both the group
and the individual levels, showed no diVerence in the performance
according to age, indicating that in dogs the comprehension
of the human pointing may require only very
limited and rapid early learning to fully develop. Interestingly,
neither the keeping conditions nor the time spent in
active interaction with the owner, and not even some special
(agility) training for using human visual cues, had signiWcant
eVect on the success and explained individual
diVerences. The performance of the dogs was rather stable
over time: during the 20 trials within a session and even
when subsamples of diVerent age were repeatedly tested.
Considering that in spite of the general success at the group
level, more than half of the dogs were not successful at the
individual level, we revealed alternative “decision-making
rules” other than following the pointing gesture of the
experimenter
Comprehension of human pointing gestures in young human-reared wolves (Canis lupus) and dogs (Canis familiaris)
Dogs have a remarkable skill to use human-given cues in object-choice tasks, but little is known to what extent their closest wild-living relative, the wolf can achieve this performance. In Study 1, we compared wolf and dog pups hand-reared individually and pet dogs of the same age in their readiness to form eye-contact with a human experimenter in an object-choice task and to follow her pointing gesture. The results showed that dogs already at 4 months of age use momentary distal pointing to find hidden food even without intensive early socialization. Wolf pups, on the contrary, do not attend to this subtle pointing. Accordingly in Studies 2 and 3, these wolves were tested longitudinally with this and four other (easier) human-given cues. This revealed that wolves socialized at a comparable level to dogs are able to use simple human-given cues spontaneously if the human's hand is close to the baited container (e.g. touching, proximal pointing). Study 4 showed that wolves can follow also momentary distal pointing similarly to dogs if they have received extensive formal training. Comparing the wolves to naive pet dogs of the same age revealed that during several months of formal training wolves can reach the level of dogs in their success of following momentary distal pointing in parallel with improving their readiness to form eye-contact with a human experimenter. We assume that the high variability in the wolves' communicative behaviour might have provided a basis for selection during the course of domestication of the dog
A nonverbal test of knowledge attribution: a comparative study on dogs and children
The sensitivity of eleven pet dogs and eleven 2.5-year-old children to others' past perceptual access was tested for object-specificity in a playful, nonverbal task in which a human Helper's knowledge state regarding the whereabouts of a hidden toy and a stick (a tool necessary for getting the out-of-reach toy) was systematically manipulated. In the four experimental conditions the Helper either participated or was absent during hiding of the toy and the stick and therefore she knew the place(s) of (1) both the toy and the stick, (2) only the toy, (3) only the stick or (4) neither of them. The subjects observed the hiding processes, but they could not reach the objects, so they had to involve the Helper to retrieve the toy. The dogs were more inclined to signal the place of the toy in each condition and indicated the location of the stick only sporadically. However the children signalled both the location of the toy and that of the stick in those situations when the Helper had similar knowledge regarding the whereabouts of them (i.e. knew or ignored both of them), and in those conditions in which the Helper was ignorant of the whereabouts of only one object the children indicated the place of this object more often than that of the known one. At the same time however, both dogs and children signalled the place of the toy more frequently if the Helper had been absent during toy-hiding compared to those conditions when she had participated in the hiding. Although this behaviour appears to correspond with the Helper's knowledge state, even the subtle distinction made by the children can be interpreted without a casual understanding of knowledge-fort-nation in others