An analysis of response,direction, and place learning in an open field and T maze

Rats were trained to locate food in a response, direction, or place problem on an open field located at 2 positions. In Experiment 1, both the response and direction groups solved the problem. The place group failed to solve the task in approximately 300 trials. Experiment 2 demonstrated that rats need distinguishable start points to solve a place problem when neither a response nor a direction solution is available. Findings from Experiment 3 suggest that a combination of path traveled and distinct cues help to differentiate start points. Experiment 4 replicated the findings using a T maze. These results suggest "place" solutions are difficult for rats. The data are discussed with respect to conditional learning and modern spatial mapping theory.     

Absence of masking in the path of apparent movement

Alternation of diagonal pairs of lights produced apparent movement which S could organize in either of two distinctly different ways, as instructed. The task was to detect movement of a weak probe light that either was or was not located in the path of the apparent movement, depending on the organization, stimulation being identical in the two cases. Results showed no evidence of path-specific masking.     

Path integration while ignoring irrelevant movement

Participants attempted to return to the origin of travel after following an outbound path by locomotion on foot (Experiments 1-3) or in a virtual visual environment (Experiment 4). Critical conditions interrupted the outbound path with verbal distraction or irrelevant, to-be-ignored movements. Irrelevant movement, real or virtual, had greater effects than verbal or cognitive distraction, indicating inability to ignore displacement during path integration. Effects of the irrelevant movement's direction (backward vs. rightward) and location (1st vs. 2nd leg of path) indicated that participants encoded a configural representation of the pathway and then cognitively compensated for the movement, producing errors directly related to the demands of compensation. An encoding-error model fit to the data indicated that backward movement produced downward rescaling, whereas movement that led to implied rotation (rightward on 2nd leg) produced distortions of shape and scale.     

Inhibition of return is composed of attentional and oculomotor processes.

Response time can be delayed if a target stimulus appears at a location or object that was previously cued. This inhibition of return (IOR) phenomenon has been attributed to a delay in activating attentional or motor processes to a previously cued stimulus. Two experiments required subjects to localize or identify a target stimulus. In Experiment 1, the subjects' eyes were not monitored. In Experiment 2, the subjects' eyes were monitored, and the subjects were instructed to either execute or withhold an eye movement to a target stimulus. The results indicated that IOR was always present for location and identification responses, supporting an attentional account of IOR. However, IOR was larger when eye movements were executed, indicating that a motor component can contribute to IOR. Finally, when eye movements were withheld, IOR was larger when a target was presented alone than when it was presented with a distractor, suggesting that IOR is larger for exogenous than for endogenous covert orienting. Together, the data indicate that IOR is composed of both an oculomotor component and an attentional component.     

Inhibition of return is composed of attentional and oculomotor processes

Response time can be delayed if a target stimulus appears at a location or object that was previously cued. This inhibition of return (IOR) phenomenon has been attributed to a delay in activating attentional or motor processes to a previously cued stimulus. Two experiments required subjects to localize or identify a target stimulus. In Experiment 1, the subjects’ eyes were not monitored. In Experiment 2, the subjects’ eyes were monitored, and the subjects were instructed to either execute or withhold an eye movement to a target stimulus. The results indicated that IOR was always present for location and identification responses, supporting an attentional account of IOR. However, IOR was larger when eye movements were executed, indicating that a motor component can contribute to IOR. Finally, when eye movements were withheld, IOR was larger when a target was presented alone than when it was presented with a distractor, suggesting that IOR is larger for exogenous than for endogenous covert orienting. Together, the data indicate that IOR is composed of both an oculomotor component and an attentional component.     

Manipulations of start and food locations affect navigation on a foraging task

Rats were able to search multiple food cups in a foraging task and successfully return to a fixed, but not a variable, start location. Reducing the number of food cups to be searched resulted in an improvement in performance in the variable start condition. Performance was better when only one or two food cups had to be visited but was still impaired if the food was not found in the first cup searched. Variable start locations impaired performance when only one food cup had to be searched, if that cup was moved over the table. These findings suggest that there is an interaction between memory processes and the navigational processes that allows an animal to return to its start location after a foraging trip. It appears that a fixed location for the food or the start point of a foraging trip is a necessary precondition for accurate performance.     

Spatial Updating Strategy Affects the Reference Frame in Path Integration

This study investigated how spatial updating strategies affected the selection of reference frames in path integration. Participants walked an outbound path consisting of three successive waypoints in a featureless environment and then pointed to the first waypoint. We manipulated the alignment of participants’ final heading at the end of the outbound path with their initial heading to examine the adopted reference frame. We assumed that the initial heading defined the principal reference direction in an allocentric reference frame. In Experiment 1, participants were instructed to use a configural updating strategy and to monitor the shape of the outbound path while they walked it. Pointing performance was best when the final heading was aligned with the initial heading, indicating the use of an allocentric reference frame. In Experiment 2, participants were instructed to use a continuous updating strategy and to keep track of the location of the first waypoint while walking the outbound path. Pointing performance was equivalent regardless of the alignment between the final and the initial headings, indicating the use of an egocentric reference frame. These results confirmed that people could employ different spatial updating strategies in path integration (Wiener, Berthoz, & Wolbers Experimental Brain Research 208(1) 61–71, 2011), and suggested that these strategies could affect the selection of the reference frame for path integration.     

Summation of response rates to discriminative stimuli associated with qualitatively different reinforcers

In Experiment I, a four-ply multiple schedule was used to study the effects on rate of responding in rats of food, water, and food and/or water reinforcement under different deprivation conditions. Food and water were associated separately with different stimuli, the combination of which was associated with food and water together, or with food or water randomly. Rates in the presence of the combined stimuli were consistently intermediate to the rates generated by the separate stimuli, a result seemingly incompatible with a "summation" hypothesis. Experiment II was a simplified systematic replication of Experiment I, verifying the major findings.     

Visual perspective taking by dogs (Canis familiaris) in a Guesser–Knower task: evidence for a canine theory of mind?

We tested domestic dogs (N = 16) in a Guesser–Knower task in which they chose between possible locations for hidden food indicated by human informants. In four experiments, the perceptual access of the Guesser and Knower to the hidden food baiting was manipulated. When informants had differing perceptual access to the baiting, dogs preferred the location indicated by the Knower from the start of testing (Experiment 1), even when baiting was done by a third experimenter (Experiments 2–3). However, when there was no difference in perceptual access and both informants either knew or did not know the food location, dogs had no preference between the informants (Experiment 4). Controls ruled out alternative explanations in terms of associative learning, unintentional and olfactory cues. Analysis of individual data showed no significant heterogeneity across dogs, and results were not correlated with age or sex. Dogs’ performances were superior to those of nonhuman primates in previous studies. Although a mentalistic explanation is not required, results add to evidence that dogs have a remarkable sensitivity to cues related to humans’ attentional state, which enables them to respond as if they had a functional theory of mind in the Guesser–Knower task with human informants.     

Drinking in a patchy environment: the effect of the price of water.

Rats in a laboratory foraging paradigm searched for sequential opportunities to drink in two water patches that differed in the bar-press price of each "sip" (20 licks) of water within a bout of drinking (Experiment 1) or the price and size (10, 20, or 40 licks) of each sip (Experiment 2). Total daily water intake was not affected by these variables. The rats responded faster at the patch where water was more costly. However, they accepted fewer opportunities to drink, and thus had fewer drinking bouts, and drinking bouts were smaller at the more costly patch than at the other patch. This resulted in the rats consuming a smaller proportion of their daily water from the more costly patch. The size of the differences in bout frequency and size between the patches appears to be based on the relative cost of water at the patches. The profitability of each patch was calculated in terms of the return (in milliliters) on either effort (bar presses) or time spent there. Although both measures were correlated with the relative total intake, bout size, and acceptance of opportunities at each patch, the time-based profitability was the better predictor of these intake measures. The rats did not minimize bar-press output; however, their choice between the patches and their bout sizes within patches varied in a way that reduced costs compared to what would have been expended drinking randomly. These data accord well with similar findings for choices among patches of food, suggesting that foraging for water and food occurs on the basis of comparable benefit-cost functions: In each case, the amount consumed is related to the time spent consuming.     

Tactile attention and the perception of moving tactile stimuli

Three experiments investigated the ability of subjects to identify the direction of movement of a pattern across the skin. In Experiments 1 and 2, subjects were required to identify the direction of movement of a pattern presented to one fingerpad while another moving pattern was being presented to an adjacent fingerpad. Subjects were instructed to attend only to the target location. The results showed that accuracy was consistently higher and reaction times were consistently faster when the two patterns moved in the same direction than when they moved in opposite directions. Both effects were largest when the two patterns were presented simultaneously. In Experiment 3, the nontarget location was the contralateral hand. In this case, performance was not affected by the presentation of the nontarget. Combined, the results suggest that movement information is processed across adjacent fingers even when subjects are explicitly instructed to attend only to one finger. Subjects do appear to be able to restrict attention to a single hand.     

Cognitive Strategies and Short-term Memory for Movement Distance and Location

A number of researchers (e.g. Kerr, 1978; Walsh, Russell, Imanaka, & James, 1979) have previously demonstrated interference between location and distance information in motor short-term memory. This interference manifests itself in a characteristic pattern of undershooting and overshooting, with reproduction movement location being drawn in the direction of criterion movement distance and, conversely, the distance of reproduction movements being influenced by the terminal location of the criterion movement. We investigated the effects of different cognitive strategies upon the appearance of this location-distance interference during the reproduction of movement location (Experiment 1) and distance (Experiments 2 and 3) in a linear arm positioning task. Experiment 1 compared performance in location reproduction between two strategy groups differing in the availability of explicit information about the change in starting position. The characteristic undershooting-overshooting interference pattern was observed for the group without the explicit information about the change in starting position but disappeared for the group in which explicit information about the change in starting position was provided. Experiment 2 examined the systematic undershooting-overshooting pattern in distance reproduction for a location strategy (involving some extrapolation of the start and end locations), a counting strategy, and a distance sense strategy (involving the use of visual imagery). The systematic response bias pattern disappeared when the subjects used a location strategy but was clearly observed for the subjects using the other two strategies. This finding was generally confirmed by Experiment 3, which showed a typical undershooting-overshooting pattern in distance reproduction for a counting/distance sense strategy but not for two location strategies (a general location and an explicit location strategy). The location strategies differed in the availability of explicit information about starting and end locations for both the criterion and reproduction movements. The results from these three experiments indicate that explicit information about the start andlor end locations prevents the usual interference between location and distance information from arising in movement reproduction. The notions of automatic and controlled processing and cerebral hemispheric specialization are discussed as potential explanations of these results and of the interference typically observed in motor short-term memory between distance and location information.     

Planning paths to multiple targets: memory involvement and planning heuristics in spatial problem solving

For large numbers of targets, path planning is a complex and computationally expensive task. Humans, however, usually solve such tasks quickly and efficiently. We present experiments studying human path planning performance and the cognitive processes and heuristics involved. Twenty-five places were arranged on a regular grid in a large room. Participants were repeatedly asked to solve traveling salesman problems (TSP), i.e., to find the shortest closed loop connecting a start location with multiple target locations. In Experiment 1, we tested whether humans employed the nearest neighbor (NN) strategy when solving the TSP. Results showed that subjects outperform the NN-strategy, suggesting that it is not sufficient to explain human route planning behavior. As a second possible strategy we tested a hierarchical planning heuristic in Experiment 2, demonstrating that participants first plan a coarse route on the region level that is refined during navigation. To test for the relevance of spatial working memory (SWM) and spatial long-term memory (LTM) for planning performance and the planning heuristics applied, we varied the memory demands between conditions in Experiment 2. In one condition the target locations were directly marked, such that no memory was required; a second condition required participants to memorize the target locations during path planning (SWM); in a third condition, additionally, the locations of targets had to retrieved from LTM (SWM and LTM). Results showed that navigation performance decreased with increasing memory demands while the dependence on the hierarchical planning heuristic increased.     

Reaction time in reading a tachistoscopic display for a memory set item

Reaction times were measured in a task which requires the subject to search a brief visual array for a critical letter embedded in a row of background letters. In Experiment 1, the position of a critical letter in an instructed reading order and the size of a set of memorized letters were varied. Mean reaction time increased monotonically with distance of the critical letter from the beginning of the instructed reading path in the display. The variables reading position and memory set size were additive in their effect on mean reaction time. Data from a second experiment in which the retinal location of the critical letter and its reading position were varied showed that both reading position and retinal location influenced mean reaction time, but the effect of reading position on reaction time was greater. These variables interacted.     

Do humans and nonhuman animals share the grouping principles of the iambic–trochaic law?

The iambic–trochaic law describes humans’ tendency to form trochaic groups over sequences varying in pitch or intensity (i.e., the loudest or highest sounds mark group beginnings), and iambic groups over sequences varying in duration (i.e., the longest sounds mark group endings). The extent to which these perceptual biases are shared by humans and nonhuman animals is yet unclear. In Experiment 1, we trained rats to discriminate pitch-alternating sequences of tones from sequences randomly varying in pitch. In Experiment 2, rats were trained to discriminate duration-alternating sequences of tones from sequences randomly varying in duration. We found that nonhuman animals group sequences based on pitch variations as trochees, but they do not group sequences varying in duration as iambs. Importantly, humans grouped the same stimuli following the principles of the iambic–trochaic law (Exp. 3). These results suggest the early emergence of the trochaic rhythmic grouping bias based on pitch, possibly relying on perceptual abilities shared by humans and other mammals, whereas the iambic rhythmic grouping bias based on duration might depend on language experience.     

Nomadic inhibition of attention and motor responses

Klein and MacInnes [Klein, R. M., & MacInnes, W. J. (1999). Inhibition of return is a foraging facilitator in visual search. Psychological Science, 10, 346-352] posited that the function of a phenomenon known as the inhibition of return (IOR) [Posner, M. I., & Cohen, Y. (1984). Components of visual orienting. In H. Bouma, & D. G. Bouwhuis (Eds.), Attention and performance X: Control of language processes (pp. 531-554). Hillsdale, NJ: Erlbaum] is to facilitate the foraging of food and objects in the environment. Once a target object has been identified either the location of that target in space or a movement to that target is inhibited in order to allow the performer to shift his/her attention to something new. Interestingly, in the majority of IOR studies, participants begin their search from a central home position. This research examined IOR in a nomadic target-target paradigm in which the home position randomly appeared at one of three target locations and attentional shifts/movements progressed to other locations. In Experiment 1, participants executed simple manual button presses in response to the sequential presentation of a home position and then two target stimuli. In Experiment 2, participants made manual-aiming movements in response to the same type of presentation. Results obtained from both experiments implicate perceptual-motor mechanisms over and above the inhibition of a specific target location or response. Inhibitory effects appear to be associated with both perceptual and motor processes, and depend not only on the temporal and spatial relations between potential targets, but also on the actions required to detect or engage the targets.     

The resistance of renewal to instructions that devalue the role of contextual cues in a conditioned suppression task with humans

The renewal of extinguished conditioned behaviour appears to reflect context-dependent learning. The present research used a conditioned suppression task with humans to examine whether instructions concerning the context could influence renewal. Pairings of a conditional stimulus (CS) and unconditional stimulus (US) were made in one context, followed by extinction trials of CS alone in a second context, and test trials of CS alone upon return to the original learning context. Four experiments tested whether the renewal of conditioned suppression observed during test would be attenuated if participants were instructed that the context changes were irrelevant to the predictive relationship between the CS and US. Using a differential conditioning design, no attenuation was found when the instructions were given prior to conditioning (Experiment 1) or immediately prior to the test trials (Experiment 2). The latter result was replicated with a single-cue conditioning design and further controls for exposure to the extinction contexts (Experiment 3). The collection of on-line ratings about the relationship between the contextual changes and the predictive nature of the CS indicated that participants did attend to and believe the instructions (Experiment 4). The results point to the resistance of renewal to explicit instructions that attempt to devalue the role of the contextual cues.     

Exploring specificity of speeded aiming movements: Examining different measures of transfer

Participants were trained and tested to move a mouse cursor from a start position to targets on a circular display in a perceptual-motor reversal condition, with horizontal, but not vertical, reversals. During training, some participants (experimental) moved to two targets either along a single diagonal axis (D1) or along both axes (D2). For D2, return movements from the targets were in the same direction as instructed movements to unpracticed targets. Others (control) trained on all targets. Testing always involved all targets. At test, movement times (to reach the target after leaving the start position) were shorter on trained than on untrained targets, especially for the D1 condition, documenting training specificity. However, movement times in the experimental conditions to new targets during testing were shorter than those in the control condition during training, documenting transfer of learning, with more transfer for D2 than for D1. Initiation times (to leave the start position after target onset) showed no transfer. The results provide evidence that specificity and transfer are not mutually exclusive and depend on the measure used to assess performance.     

Optimal combination of environmental cues and path integration during navigation

Navigation is influenced by body-based self-motion cues that are integrated over time, in a process known as path integration, as well as by environmental cues such as landmarks and room shape. In two experiments we explored whether humans combine path integration and environmental cues (Exp. 1: room shape; Exp. 2: room shape, single landmark, and multiple landmarks) to reduce response variability when returning to a previously visited location. Participants walked an outbound path in an immersive virtual environment before attempting to return to the path origin. Path integration and an environmental cue were both available during the outbound path, but experimental manipulations created single- and dual-cue conditions during the return path. The response variance when returning to the path origin was reduced when both cues were available, consistent with optimal integration predicted on the basis of Bayesian principles. The findings indicate that humans optimally integrate multiple spatial cues during navigation. Additionally, a large (but not a small) cue conflict caused participants to assign a higher weight to path integration than to environmental cues, despite the relatively greater precision afforded by the environmental cues.