Learning & Behavior最新文献

Fear and anxiety are rarely confined to specific stimuli or situations. In fear generalisation, there is a spread of fear responses elicited by physically dissimilar generalisation stimuli (GS) along a continuum between danger and safety. The current study investigated fear generalisation with a novel online task using COVID-19-relevant stimuli (i.e., busy or quiet shopping street/mall scenes) during pandemic lockdown restrictions in the United Kingdom. Participants (N = 50) first completed clinically relevant trait measures before commencing a habituation phase, where two conditioned stimuli (CSs; i.e., a busy or quiet high street/mall scene) were presented. Participants then underwent fear conditioning where one conditioned stimulus (CS+) was followed by an aversive unconditioned stimulus (US; a loud female scream accompanied by a facial photograph of a female displaying a fearful emotion) and another (CS-) was not. In a test phase, six generalisation stimuli were presented where the US was withheld, and participants provided threat expectancy and fear ratings for all stimuli. Following successful conditioning, fear generalization was observed for both threat expectancy and fear ratings. Trait worry partially predicted generalised threat expectancy and COVID-19 fear strongly predicted generalised fear. In conclusion, a generalisation gradient was evident using an online remote generalisation task with images of busy/quiet streets during the pandemic. Worry and fear of COVID-19 predicted fear generalisation.

Previous experiments found that acceptance of saccharin by rats was reduced if they had prior experience of sucrose or some other highly palatable solution. This study tested whether such successive negative contrast (SNC) effects involve acquisition of an aversion to the new taste. In three experiments, rats were switched from sucrose exposure in Stage 1 to a less palatable solution containing a new taste in Stage 2. In Experiments 1 and 2, a novel flavor was added to a saccharin solution at the start of Stage 2. In Experiment 1, preference tests revealed a weak aversion to the added vanilla flavor in the Suc-Sacch group, while in Experiment 2 an aversion was found in the Suc-Sacch group to the salty flavor that was used, compared with controls given access either saccharin or water in Stage 1. In Experiment 3, the Suc-Quin group, given quinine solution in Stage 2, displayed a greater aversion to quinine than a Water-Quin control group. These results support the suggestion that taste aversion learning plays a role in the initial suppression of intakes in a qualitative consummatory SNC effect. However, in the light of other evidence, it seems that the unusual persistence of successive negative contrast when rats are switched from sucrose to saccharin is not due to a long-lasting reduction in the value of saccharin.

A recent study by Johnston, Brecht, and Nieder (2023, Current Biology, 33, 3238-3243) finds that carrion crows associate varying rates of reinforcement with novel arbitrary stimuli and make optimal decisions when they must later choose between stimulus pairs. These results demonstrate that crows are capable of not only storing information about reward probabilities in their memory but also making optimal choices based on this information even a month later.

The midsession reversal task involves a simultaneous discrimination between stimuli S1 and S2. Choice of S1 but not S2 is reinforced during the first 40 trials, and choice of S2 but not S1 is reinforced during the last 40 trials. Trials are separated by a constant intertrial interval (ITI). Pigeons learn the task seemingly by timing the moment of the reversal trial. Hence, most of their errors occur around trial 40 (S2 choices before trial 41 and S1 choices after trial 40). It has been found that when the ITI is doubled on a test session, the reversal trial is halved, a result consistent with timing. However, inconsistent with timing, halving the ITI on a test session did not double the reversal trial. The asymmetry of ITI effects could be due to the intrusion of novel cues during testing, cues that preempt the timing cue. To test this hypothesis, we ran two types of tests after the regular training in the midsession reversal task, one with S1 and S2 choices always reinforced, and another with S1 always reinforced but S2 reinforced only after 20 trials when the ITI doubled or 40 trials when the ITI halved. For most pigeons, performance was consistent with timing both when the ITI doubled and when it was halved, but some pigeons appeared to follow strategies based on counting or on reinforcement contingencies.

Zebrafish exhibit fear contagion, a basic form of empathy, and when observing social fellows that have been exposed to predation cues, will themselves exhibit similar distress behaviours. As in mammals, the nonapeptide hormone oxytocin is essential for this empathic response, and homologous areas of the brain are involved, suggesting that the mechanistic basis of empathy may be conserved among vertebrates.

When seeing a visual image, humans prioritize the perception of global features, which is followed by the assessment of the local ones. This global precedence has been investigated using hierarchical stimuli that consist of a large, global shape formed by the spatial arrangement of small local shapes. Comparing non-human animals to humans, research on global and local processing has revealed a heterogeneous pattern of results with some species exhibiting a local precedence and others a global one. Many factors have been proposed to influence the global and local processing: internal factors (e.g., age, sex) and external elements or perceptual field variables (e.g., stimulus size, visual angle, eccentricity, sparsity). In this review, studies showing that different non-human species process hierarchical stimuli in the same (global precedence) or reverse (local precedence) direction as humans are first collated. Different ecological, perceptual, and anatomical features that may influence global and local processing are subsequently proposed based on a detailed analysis of these studies. This information is likely to improve our understanding of the mechanisms behind the perceptual organization and visual processing, and could explain the observed differences in hierarchical processing between species.

North African desert ants Cataglyphis fortis living on a featureless saltpan far from the shoreline build a mound at their nest entrance. Experimental manipulations show that they do this purposefully to make it easier for returning foragers to find their nest.

The waggle dance of honey bees is a classic example of complex behavior and communication in animals. Despite long being considered a completely fixed and innate behavior, recent work is showing a role for social learning in tuning components of the waggle dance in naïve bees.

Memory for what, where, and when an event took place has been interpreted as playing a critical role in episodic memory. Moreover, such memory is likely to be important to an animal's ability to efficiently forage for food. In Experiment 1 of the present study, pigeons were trained on a task in which on each trial, one lit stimulus color and location was presented and then another. A cue presented after the last stimulus location signaled that the pigeon was to choose either the first location presented, or the last location presented, to receive a reinforcer. After learning this task, in Experiment 2, the color cue was removed, requiring the pigeons to choose based on location and order alone. In Experiment 3, when a delay was inserted between presentation of the two locations, it had little effect on task accuracy. Results suggested that the pigeons had acquired the task using a single-code/default rule. When presented with the cue indicating that the last location was correct, pigeons selected the location just presented. When presented with the cue indicating that the first location was correct, pigeons chose the other location, by default. In support of this hypothesis, in Experiment 4, when a delay was inserted, prior to receiving the instructional cue, it had a disruptive effect on task accuracy proportional to the delay. Although the present results do not provide evidence for episodic memory, they do suggest that the pigeons have developed a single-code/default strategy that appears to be an efficient means of performing this task.

Previous studies have shown that whip spiders (Amblypygi) can use a variety of cues to navigate to and recognize a home refuge. The current study aimed to determine whether whip spiders were capable of using the boundary geometry of an experimental space (geometric information) to guide goal-directed navigation and to investigate any preferential use of geometric or feature (visual) information. Animals were first trained to find a goal location situated in one corner of a rectangular arena (geometric information) fronting a dark-green-colored wall, which created a brightness contrast with the other three white walls (feature information). Various probe trials were then implemented to determine cue use. It was found that animals were capable of directing their choice behavior towards geometrically correct corners at a rate significantly higher than chance, even when the feature cue was removed. By contrast, choice behavior dropped to random chance when geometric information was removed (test in a square arena) and only feature information remained. Choice behavior was also reduced to chance when geometric and feature information were set in conflict (by moving the feature cue to one of the longer walls in the rectangular arena). The data thus suggest that whip spiders are capable of using geometric information to guide goal-directed navigation and that geometric information is preferred over feature guidance, although a feature cue may set the context for activating geometry-guided navigation. Experimental design limitations and future directions are discussed.