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ABSTRACTS
Cheng, Ken; Spetch, Marcia L.
Source
Learning & Motivation. Vol 33(3) Aug 2002, 358-389.
Academic Press, US
Abstract
Using a computer betting game, five experiments tested male and female university
students (aged 17-44 yrs) on spatial generalization and peak shift. On each
trial, one location was marked and the subject was invited to bet 0-4 points.
At the winning location (S+), bets won four times the points betted. At nearby
losing locations (S-s), points betted were lost. Generalization gradients were
exponential in shape, supporting R. N. Shepard's (1987), law (Experiment 1).
With peak shift manipulations, three kinds of peak shift or area shift were
found. Subjects betted more on the S+ side than on the S- side (Experiments
2-4). When asked if a location was the winning location, subjects responded
"yes' more often to locations on the S+ side than to locations on the S-
side (Experiments 3-5). When asked to point to the winning location on the screen,
subjects' errors indicated peak shift (Experiment 5).
Spetch, Marcia L; Friedman, Alinda; Reid, Sheri L.
Source
Journal of Experimental Psychology: General. Vol 130(2) Jun 2001, 238-255.
American Psychological Assn, US
Abstract
To explore whether effects observed in human object recognition represent fundamental
properties of visual perception that are general across species, the authors
trained pigeons (Columba livia) and humans to discriminate between pictures
of 3-dimensional objects that differed in shape. Novel pictures of the depth-rotated
objects were then tested for recognition. Across conditions, the object pairs
contained either 0, 1, 3, or 5 distinctive pails. Pigeons showed viewpoint dependence
in all object-part conditions, and their performance declined systematically
with degree of rotation from the nearest training view. Humans showed viewpoint
invariance for novel rotations between the training views but viewpoint dependence
for novel rotations outside the training views. For humans, but not pigeons,
viewpoint dependence was weakest in the 1-part condition. The authors discuss
the results in terms of structural and multiple-view models of object recognition.
Cheng, Ken; Spetch, Marcia L.
Source
Animal Learning & Behavior. Vol 29(1) Feb 2001, 1-9.
Psychonomic Society, US
Abstract
Two experiments tested blocking in landmark-based search in honeybees. Honeybees
in the experimental group were trained in Phase 1 with a single landmark in
a constant spatial relation to the target (sugar water). In the compound training
second phase, the landmark used in Phase 1 (blocking landmark) and a new landmark
(blocked landmark) were presented at constant spatial relations to the target.
The blocking and blocked landmarks differed from each other in color and position,
and the blocking landmark retained the same spatial relationship to the target
as in Phase 1. In Exp 1, the control group experienced only Phase 2 training
with 2 landmarks. In Exp 2, the control group was trained with a different landmark
in a different position in Phase 1. Blocking was found in both cases.
Kelly, Debbie M; Spetch, Marcia L.
Source
Journal of Experimental Psychology: Animal Behavior Processes. Vol 27(4) Oct
2001, 417-422.
American Psychological Assn, US
Abstract
Pigeons were trained to search for hidden food in a rectangular environment
designed to eliminate any external cues. Following training, the authors administered
unreinforced test trials in which the geometric properties of the apparatus
were manipulated. During tests that preserved the relative geometry but altered
the absolute geometry of the environment, the pigeons continued to choose the
geometrically correct corners, indicating that they encoded the relative geometry
of the enclosure. When tested in a square enclosure, which distorted both the
absolute and relative geometry, the pigeons randomly chose among the 4 corners,
indicating that their choices were not based on cues external to the apparatus.
This study provides new insight into how metric properties of an environment
are encoded by pigeons.
Kelly, Debbie M; Bischof, Walter F; Wong-Wylie, Douglas R; Spetch, Marcia L.
Source
Psychological Science. Vol 12(4) Jul 2001, 338-342.
Blackwell Publishers, US
Abstract
Glass patterns have been used to examine mechanisms underlying form perception.
The current investigation compared detection of glass patterns by pigeons and
humans and provides evidence for substantial species differences in global form
perception. Ss were required to discriminate, on a simultaneous display, a random
dot pattern from a Glass pattern. Four different randomly presented glass patterns
were used (concentric-, radial, parallel-vertical, and parallel-horizontal).
Detection thresholds were measured by degrading the glass patterns through the
addition of random noise. For both humans and pigeons, discrimination decreased
systematically with the addition of noise. Humans showed detection differences
among the four patterns, with lowest thresholds to radial and concentric patterns
and highest thresholds to the parallel-horizontal pattern. Pigeons did not show
a detection difference across the four patterns. Implications for differences
in neural processing of complex forms are discussed.
Spetch, Marcia L; Kelly, Debbie M; Reid, Sheri.
Source
Fagot, Joel (Ed). (2000). Picture perception in animals. (pp. 107-141). xii,
447pp.
Abstract
(from the chapter) Examined an animals' ability to recognize objects or places
in static pictures across changes in view. In Exp 1, pigeons with prior outdoor
experience OE) were trained to locate an unmarked goal in 6 views of a scene
presented on a touch-screen monitor. The goal location was fixed relative to
landmarks in the scene, but 2-D vectors from landmarks to the goal varied across
views. Pigeons learned the task, but showed poor transfer to novel views. Their
performance resembled that previously seen in laboratory raised pigeons with
the same images, but differed from that previously seen in outdoor-experienced
pigeons trained with more views of a different scene. Thus, stimulus and/or
training factors, rather than OE, may determine degree of transfer to novel
views. Exp 2 explored pigeons' object recognition across changes in viewpoint.
One group discriminated objects composed of identical parts and another group
discriminated objects composed of different parts. Baseline accuracy was higher
for the different-parts group, but transfer to novel views was comparable across
groups. Both groups generalized across views, but accuracy decreased with rotation
from the nearest training view. Implications for the use of pictorial stimuli
to study cognitive processes in animals are discussed.
Kelly, Ronald; Spetch, Marcia L.
Source
Quarterly Journal of Experimental Psychology B. Vol 53B(4) Nov 2000, 309-323.
Taylor & Francis/Psychology Press, England
Abstract
Two experiments investigated the effect of similarity between intertrial interval
(ITI) and delay illumination on the choose-short effect. Different groups of
pigeons learned to match "short" (2 s) and "long" (6 or
8 s) food samples to green and red test stimuli in a matching-to-sample procedure
with a 5-s training delay. Subsequent 10- and 20-s delay tests revealed choose-short
effects if the ITI and delay were both illuminated (i.e., group On-On), if the
ITI and delay were both dark (i.e., group OFF-OFF), and if the ITI was illuminated
and the delay was dark (i.e., group ON-OFF). In addition, either a choose-short
effect or a choose-long effect was observed if the ITI was dark and the delay
was illuminated (i.e., group OFF-ON). Results are incompatible with the confusion/instructional
failure view of the choose-short effect.
Spetch, Marcia L; Kelly, Debbie M; Reid, Sheri.
Source
Cahiers de Psychologie Cognitive. Vol 18(5-6) Oct-Dec 1999, 729-764.
CPC, France
Abstract
Examined the ability of pigeons to extract information from pictures, to discriminate
between depicted objects, and to generalize to novel viewpoints. In Exp 1, 4
pigeons with prior outdoor experience were trained with images to locate an
unmarked goal in 6 views. Results show the pigeons learned the task, but demonstrated
poor transfer to novel views. Comparison with results of a previous study show
that stimulus and training factors rather than outdoor experience may determine
degree of transfer to novel views. In Exp 2, 4 pigeons of Group 1 discriminated
objects composed of identical parts, while 5 pigeons of Group 2 discriminated
objects composed of different parts. Results show that both groups of Ss generalized
across views, with accuracy of novel views decreasing systematically as a function
of rotation from the nearest training value. The higher accuracy for Ss in the
different-parts group indicates that the distinctive parts facilitated the discrimination
between the objects, but did not produce viewpoint invariance. Though it is
appropriate to use pictorial stimuli in many animal studies, it is concluded
that static pictorial stimuli are impoverished in numerous ways relative to
the visual information available to pigeons in the real world.
Bischof, Walter F; Reid, Sheri L; Wylie, Doug R. W; Spetch, Marcia L.
Source
Perception & Psychophysics. Vol 61(6) Aug 1999, 1089-1101.
Psychonomic Society, US
Abstract
Compared motion sensitivity in 8 pigeons and 4 human Ss by requiring both species
to discriminate coherent from random motion in dynamic random dot displays.
Coherence and velocity thresholds were determined for both species, and both
thresholds were found to be substantially higher for pigeons than for humans.
The results are discussed with reference to differences in motion processing
in mammals and birds. It is suggested that the inferior motion sensitivity of
pigeons can be attributed to poorer spatiotemporal motion integration.
Kelly, Ronald; Spetch, Marcia L; Grant, Douglas S.
Source
Journal of Experimental Psychology: Animal Behavior Processes. Vol 25(3) Jul
1999, 297-307.
American Psychological Assn, US
Abstract
The effects of procedural modifications of choice and successive matching tasks
on retention of event duration (2- and 10-sec presentations of light) were examined.
In accord with prior results, retention testing revealed that accuracy on short-
and long-sample trials declined symmetrically in standard successive matching
but asymmetrically (i.e., markedly on long-sample trials, and very little on
short-sample trials) in standard choice matching. Moreover, asymmetrical retention
functions were also obtained in (1) a modified successive task in which all
trials ended in reinforcement and (2) a modified choice task in which the penalty
for incorrect responding was substantially reduced. It was concluded that pigeons
code duration analogically in both standard choice and successive matching tasks,
and that such coding is manifest in asymmetrical retention functions only in
the absence of a response bias engendered by the standard successive procedure.
Source
Psychonomic Bulletin & Review. Vol 5(4) Dec 1998, 698-704.
Psychonomic Society, US
Abstract
Pigeons were trained to discriminate pictures of intact objects from pictures
of objects in which both depth from shading and depth from perspective cues
were manipulated. Depth from shading was manipulated either by scrambling or
by removing three-dimensional shading cues. Depth from perspective was manipulated
either by presenting pictures of objects with a two-dimensional outline (i.e.,
a square) or with a three-dimensional outline (i.e., a cube). Transfer tests
with novel images suggest that pigeons perceive and utilize both types of pictorial
depth cues.
Kelly, Debbie M; Spetch, Marcia L; Heth, C. Donald.
Source
Journal of Comparative Psychology. Vol 112(3) Sep 1998, 259-269.
American Psychological Assn, US
Abstract
Pigeons (Columba livia) searched for hidden food in a rectangular environment
constructed to eliminate external orientation cues. A feature group was initially
trained with distinct features in each corner. A geometric group was initially
trained with no featural information. Tests revealed that both groups encoded
the geometry of the apparatus. The geometric group was then retrained with features,
and a series of tests was administered to both groups. Transformation tests
revealed that the groups differed in reliance on features versus geometry. Pigeons
in the feature group followed the positive feature even when it was placed in
a geometrically incorrect corner, whereas pigeons in the geometric group showed
shared control by features and geometry. Both groups were able to use features
in corners distant to the goal to orient themselves, and both groups relied
more on the color than on the shape of the features.
Source
Healy, Sue (Ed). (1998). Spatial representation in animals. (pp. 1-17). x, 188pp.
Abstract
(from the chapter) Summarises work on landmark-based spatial memory in several
species of vertebrates. The authors review the transformational approach to
the study of landmark-based spatial memory, and extant data on 3 themes: (1)
the use of metric properties of distances and directions; (2) the use of multiple
cues; and (3) the use of configurations of landmarks. The review indicates that
all vertebrate species that have been studied use metric properties in localisation.
On transformations of landmark arrays, participants search in locations that
preserve some metric properties, although different species might preserve different
properties. With multiple landmarks in the array, participants often use more
than one cue or element in searching. Evidence indicates that all vertebrate
species use the configuration of landmarks, whereas honey-bees seem to use an
elemental system.
Spetch, Marcia L; Cheng, Ken.
Source
Animal Learning & Behavior. Vol 26(1) Feb 1998, 103-118.
Psychonomic Society, US
Abstract
In 4 experiments, the authors examined stimulus generalization and the peak
shift effect in the temporal dimension in 8 pigeons. Pigeons were reinforced
for pecking a key following 1 signal duration (S+), but not following another
signal duration (S-). The S+ and S- were 2.52 and 5.67 sec, respectively, counterbalanced
across birds. Subsequent generalization tests with a range of signal durations
revealed a step function, with high response rates for all durations on the
S+ side of the distribution, low response rates for all durations on the S-
side, and an intermediate rate for the intermediate duration. A comparison group
of pigeons trained with only the S+ duration showed a flat generalization function.
For the discrimination trained birds, the delay between signal termination and
opportunity to respond was subsequently varied during generalization testing.
A step function again appeared, and no evidence of subjective shortening over
the delay was found. The overall pattern of results suggests that the birds
categorized the temporal signal into 2 classes and retained a categorical code
over the delay.
Spetch, Marcia L; Kelly, Debbie M; Lechelt, David P..
Source
Animal Learning & Behavior. Vol 26(1) Feb 1998, 85-102.
Psychonomic Society, US
Abstract
Investigated pigeons' spatial search in images of outdoor scenes that included
landmarks near the goal and a visually rich set of background cues. Nine pigeons
and, for comparison, 19 18-47-yr-olds searched for an unmarked goal in digitized
images of an outdoor scene presented on a touch-screen monitor. In Exp 1, the
scene contained 3 landmarks near the goal and a visually rich background. Six
training images presented the scene from different viewing directions and distances.
Subsequent unreinforced tests in which landmark or background cues were removed
or shifted revealed that the pigeons' search was controlled by both proximal
landmarks and background cues, whereas humans relied only on the proximal landmarks.
Pigeons' search accuracy dropped substantially when they were presented with
novel views of the same scene, whereas humans showed perfect transfer to novel
views. In Exp 2, pigeons with previous outdoor experience and humans were trained
with 28 views of an outdoor scene. Both pigeons and humans transferred well
to novel views of the scene. This positive transfer suggests that, under some
conditions pigeons, like humans, may encode the 3-dimensional spatial information
in images of a scene.
Margaret A. McDevitt, University of California, San Diego
Marcia L. Spetch, University of AlbertaRoger Dunn, San Diego State University
In a baseline condition, pigeons chose between an alternative that always provided
food following a 30-s delay (100% reinforcement), and an alternative that provided
food half of the time and blackout half of the time following 30-s delays (50%
reinforcement). On average, each alternative was chosen approximately equally
often, replicating the finding of suboptimal choice in probabilistic reinforcement
procedures. The efficacy of the delay stimuli as conditioned reinforcers was
assessed in other conditions by interposing a 5-s gap period between the choice
response and one or more of the delay stimuli. The strength of conditioned reinforcement
was measured by the decrease in choice of an alternative when the alternative
contained a gap. Preference for the 50% alternative decreased in conditions
in which the gap preceded all delay stimuli, both 50% delay stimuli, and the
50% food stimulus, but preference was not consistently affected in conditions
in which the gap preceded only the 100% delay stimulus or the 50% blackout stimulus.
These results support the notion that conditioned reinforcement underlies the
finding of suboptimal preference in probabilistic reinforcement procedures,
and that the signal for food on the 50% reinforcement alternative functions
as a stronger conditioned reinforcer than the signal for food on the 100% reinforcement
alternative. In addition, the results fail to provide evidence that the signal
for blackout functions as a conditioned punisher.
Marcia L. Spetch, Debbie M. Kelly and David P. Lechelt
University of Alberta
Pigeons and adult humans searched for a 2 cm square unmarked
goal in digitized images of an outdoor scene presented on a touch-screen monitor.
In Experiment 1, the scene contained three landmarks near the goal and a visually
rich background. Six training images presented the scene from different viewing
directions and distances. Subsequent unreinforced tests in which landmark or
background cues were removed or shifted revealed that pigeons' search was controlled
by both proximal landmarks and background cues, whereas humans relied only on
the proximal landmarks. Pigeons's search accuracy dropped substantially when
they were presented with novel views of the same scene, whereas humans showed
perfect transfer to novel views. In Experiment 2, pigeons with previous outdoor
experience and humans were trained with 28 views of an outdoor scene. Both pigeons
and humans transferred well to novel views of the scene. This positive transfer
suggests that under some conditions pigeons, like humans, may encode the three-dimensional
spatial information in images of a scene
Ken Cheng
Macquarie University
Marcia L. Spetch and Michael Johnston
University of Alberta
These experiments examined how pigeons generalize across
spatial locations. During training, a square was presented at a fixed height
at one of two horizontal locations on a monitor screen. One location (S+) signaled
reward while the other one (S-) signaled no reward. The birds were then tested
occasionally with a range of locations. After training with S+ only, the generalization
gradient peaked at S+ and was approximately Gaussian in shape. After training
with equal numbers of S+ and S- trials, response rates were higher on the S+
side of the distribution. This asymmetry diminishing over testing. When the
S+ and S- were close together, the peak of responding was shifted on initial
generalization tests. Generalization gradients along the orthogonal vertical
dimension were approximately exponential in shape. This is the first demonstration
of generalization and peak shift in the spatial domain.
David P. Lechelt and Marcia L. Spetch
University of Alberta
Pigeons were trained in a touch-screen task and in an
open-field task to search for a hidden goal using an array of landmarks to guide
their search behavior. The touch-screen task presented digitized images of the
open field landmarks and environment. Upon completion of training in each task,
tests involving the alteration, shifting, or removal of landmarks were conducted
to determine which landmark(s) and stimulus feature(s) controlled search behavior.
In both tasks, proximity to the goal was an important determinant of landmark
control. The overall patterns of landmark control showed both similarities and
differences in the two tasks. No evidence was obtained that learning about the
arrangement of landmarks and goal transferred across the two tasks.
Ken Cheng, School of Behavioural Sciences Macquarie University
Marcia L. Spetch, Department of Psychology University of Alberta
We have reviewed the transformational approach to the study of landmark-based spatial memory, and extant data on three themes: the use of metric properties of distances and directions, the use of multiple cues, and the use of configurations of landmarks. In the transformational approach, the participant has the task of locating a target with respect to an experimentally provided set of landmarks. Often the experimental set is moved about from trial to trial to ensure that the target is in a constant location only with respect to the experimental landmarks, and not to anything else. On crucial unrewarded tests, the experimental landmarks are transformed in theoretically motivated ways to find out something about how the participants use landmarks in localisation.
Our review indicates that all vertebrate species that have been studied use metric properties in localisation. On transformations of landmark arrays, participants search in locations that preserve some metric properties, although different species might preserve different properties. In pigeons, evidence indicates that distances and directions are computed separately and independently.
With multiple landmarks in the array, participants often use more than one cue or element in searching. However, when other cues provide a stable directional frame of reference, control of searching is sometimes restricted to a single element of a landmark array. We reviewed parallels between landmark learning and other forms of learning in general. Participants prefer to rely on better predictors, those landmarks that are closer to the goal. Moreover, relative distances from goal to landmarks matter. A landmark at a particular absolute distance is overshadowed by a landmark that is nearer to the goal. Testing for other general laws of learning in landmark-based search forms a worthwhile research program.
By the use of configuration, we mean more than using multiple
landmarks. The participant must encode some relationship between landmarks.
An elemental solution encodes only relations between the target and single landmarks.
Evidence indicates that all vertebrate species use the configuration of landmarks,
whereas honeybees seem to use an elemental system. Adult humans differ from
other species in the use of configuration. They use abstract geometric rules
such as "search in the middle of the array". The entire area of the
use of configuration deserves more investigation.
Douglas S. Grant, Marcia L. Spetch, and Ronald Kelly
University of Alberta
A fundamental issue in the analysis of working memory is the nature of the representation, or code, that mediates accurate performance across a retention interval. In this chapter we addressed the nature of working memory representations in DMTS tasks in which the samples differ in duration. In the standard choice version of the DMTS task, in which each duration sample is mapped in a one-to-one relation to a comparison stimulus, naive pigeons code samples retrospectively and analogically. We maintain that, in such instances, pigeons represent different event durations as codes which specify values along a dimension that changes in a continuous and cumulative manner as a function of the passage of time. Such a coding process is analogical because the representative dimension shares with duration the property of changing in a continuous and cumulative manner. As one example of an analogical-coding process, pigeons might represent different durations as different intensities of a visual image. On this view, the intensity of the image increases as time spent in the presence of the sample increases, and decreases as time since termination of the sample increases. The phenomena considered in the first major section of this chapter encourage the view that durations are coded analogically, and discourage the view that durations are coded asymmetrically or categorically (either retrospectively or prospectively).
Research considered in the second major section of this chapter suggests, however, that duration samples are not always coded analogically. In the successive DMTS task, in which accuracy is assessed by a go/no-go response rather than by choice behavior, duration samples are coded nonanalogically, perhaps in an instructional, prospective manner. Evidence of nonanalogical coding of duration samples has also been obtained in two instances in the choice DMTS task. First, pigeons initially trained in successive DMTS demonstrate nonanalogical coding when subsequently transferred to a choice DMTS task in which the contingencies are consistent with those of prior training. Substantial positive transfer from successive to choice DMTS suggests that pigeons continue to use the nonanalogical coding process adopted in the successive task when transferred to the choice task. Second, pigeons trained with two sets of samples, either both temporal or one temporal and one nontemporal, mapped onto a single set of comparisons (an MTO mapping) also demonstrate nonanalogical coding of the temporal samples. The results of mediated transfer testing suggest that samples associated with the same comparison stimulus activate a common code (e.g., "peck red", "event A"). One caveat to this conclusion is that an MTO mapping is less likely to reduce the tendency to code temporal samples analogically if accurate matching with temporal samples is acquired prior to acquiring accurate matching with nontemporal samples.
In summary, substantial progress has been made over the
past decade in identifying the coding processes used by pigeons in DMTS tasks
with duration samples, and in determining some of the factors that induce analogical
or nonanalogical forms of coding. As yet, however, less is known about the generality
of these results across species (e.g., Santi, Weise & Kuiper, 1995) or the
coding processes used in other types of tasks that may require retention of
temporal information.
Marcia L. Spetch, University of Alberta
Ken Cheng, University of Toronto
Suzanne E. MacDonald, York University
Brie A. Linkenhoker, Transylvania University
Debbie M. Kelly and Sharon R. Doerkson, University of Alberta
Pigeons and humans searched for a goal that was hidden
in varied locations within a search space. The goal location was fixed relative
to an array of identical landmarks. Pigeons searched on the laboratory floor
and humans searched on a table top, or an outdoor field. In Experiment 1, the
goal was centered in a square array of 4 landmarks. When the spacing between
landmarks was increased, humans searched in the middle of the expanded array,
whereas pigeons searched in locations that preserved distance and direction
to an individual landmark. In Experiment 2, the goal was centered between and
a perpendicular distance away from 2 landmarks aligned in the left/right dimension.
When landmark spacing was increased, humans, but not pigeons, shifted their
searching away from the landmarks along the perpendicular axis. These results
parallel those obtained in touch-screen tasks. Pigeons and humans differ in
how they use landmark configuration.
Marcia L. Spetch
University of Alberta
Ken Cheng
University of Toronto
Suzanne E. MacDonald
York University
Pigeons and humans searched on a touch-screen monitor
for an unmarked goal located relative to an array of landmarks presented in
varied screen locations. After training with the goal centered in various square
arrays of four landmarks, humans, but not pigeons, transferred accurately to
arrays with novel elements. Humans searched in the middle of expanded arrays,
whereas pigeons preserved the distance and direction to a single landmark. When
trained with the goal centered below two identical horizontally aligned landmarks,
humans responded to horizontal expansions or contractions of the array by shifting
their search vertically, preserving angles from landmarks to goal. Pigeons did
not adjust their search vertically. Humans trained with a single landmark adjusted
search distance when landmark size was changed. Both pigeons and humans use
the configuration of a landmark array, but the underlying processes seem to
differ.
Ken Cheng, University of Toronto
Marcia L. Spetch, University of Alberta
Paul Miceli, University of Toronto
Pigeons and humans performed on a task in which spatial
position and elapsed time redundantly signaled the availability of reward. On
each training trial, a landmark moved steadily across the monitor screen. After
a fixed amount of time and movement, reward was available for a response. On
occasional unrewarded tests, the landmark moved at 0.50, 0.75, 1.00, 1.50, or
2.00 times the training speed. In both pigeons and humans, the central tendency
in the response distribution on tests differed across speeds, when measured
in terms of both elapsed time, and landmark position. Pigeons and humans seem
to average a duration of time and a spatial position to come up with a single
criterion time-place that corresponds to the expected time-place of reward.
Marcia L. Spetch, Douglas S. Grant and Ronald Kelly
University of Alberta
Pigeons' retention functions for duration samples differ
qualitatively in choice and successive delayed-matching-to-sample tasks. This
research tested procedures designed to be hybrids of these tasks. In Experiment
1, adding a fixed-interval component to the test phase of the choice procedure
did not eliminate the "respond- short" effect that is characteristic
of retention functions for duration in the choice task. A respond-short effect
was not present after the birds were subsequently trained in the successive
task. In Experiment 2, a choice component was added to the successive task by
providing an option stimulus that could be selected to obtain reinforcement
on S- trials that followed either short or long samples. Pigeons showed a respond-short
effect under this successive-option procedure but did not show a respond-short
effect after training with the option stimulus removed from the successive procedure.
Thus, the different retention functions obtained in choice versus successive
tasks do not appear to reflect differences in the temporal aspect of the test
stimulus schedule or the successive versus simultaneous viewing of the test
stimuli. Instead, a respond-short effect emerges when subjects make a choice
response based on sample duration, but not when they make a go/no-go response
based on sample duration.
Marcia L. Spetch
University of Alberta
Overshadowing in landmark learning was investigated in
both pigeons and undergraduate students using a touch-screen spatial search
task. Ss searched for an unmarked goal presented in varied locations on a computer
screen. Graphic stimuli served as landmarks. The effect of the presence of other
landmarks on the control acquired by a given landmark was assessed using a design
in which each S was trained with 2 sets of landmarks. Both pigeons (Experiment
1) and humans (Experiments 2-4) showed evidence of learning more about a landmark
that was the closest landmark of its set to the goal than about a landmark that
was of equal distance to the goal but was not the closest landmark of its set.
That is, control by a landmark was overshadowed when it occurred together with
a landmark that was closer to the goal. Landmark effectiveness appears to depend
not only on the absolute properties of a landmark, but on relative factors.
The relevance of basic principles of associative learning to spatial landmark
learning is discussed.
Ken Cheng, University of Toronto
Marcia L. Spetch, University of Alberta
Pigeons were tested in a search task on the surface of
a monitor on which their responses were registered by a touch-sensitive device.
A graphic landmark array was presented consisting of a square outline (the frame)
and a colored "landmark". The unmarked goal, pecks at which produced
reward, was located near the center of one edge of the frame, and the landmark
was near it. The entire array was displaced without rotation on the monitor
from trial to trial. On occasional no-reward tests, the following manipulations
were made to the landmark array: (1) either the frame or the landmark was removed;
(2) either one edge of the frame or the landmark was shifted; and (3) two landmarks
were presented with or without the frame present. On these two-landmark tests,
the frame, when present, defined which was the 'correct' landmark. When the
frame was absent, the 'correct' landmark was arbitrarily determined. Results
showed that pecks of 2 pigeons were controlled almost solely by the landmark,
pecks of 3 were controlled primarily by the landmark but the frame could distinguish
the correct landmark, and 1 bird's behavior was controlled primarily by the
frame. Stimulus control in this search task is thus selective and differs across
individuals. Comparisons to other search tasks and to other stimulus control
experiments are made.
Marcia L. Spetch, University of Alberta
Donald M. Wilkie, University of British Columbia
Pigeons received food for pecking a hidden goal location
in digitized images of an outdoor scene, presented on a monitor/touchscreen
system. Three landmarks (tree, flowers, log) were located near the goal on a
field of grass. For some birds the goal was closest to the tree, whereas for
other birds the goal was closer to the flower and log. After training, the landmarks
were removed, shifted or altered using imaging software. Landmark control was
highly selective, and depended on proximity to the goal. There was no evidence
that search was controlled by the configuration of the three landmarks. Instead,
search behavior appeared to be jointly controlled by a single local landmark
and global cues associated with the area of the screen that contained goal locations
during training. These findings extend results of a previous study that used
simple graphic forms as landmarks in a touch-screen task, and they demonstrate
the use of video imaging technology for studies of spatial landmark learning.
Douglas S. Grant and Marcia L. Spetch
University of Alberta
Pigeons were trained on two independent matching-to-duration-samples
tasks; one involved 2- and 10-s durations and color choice stimuli, and the
other involved 4.5- and 22.5-s durations and line choice stimuli. Accuracy was
above chance on mixed-choice probes in which either of the short-duration samples
was followed by the two short-associated stimuli. Following explicit training
on mixed-choice trials involving choice between the two short- and the two long-associated
stimuli, a choose-short effect was demonstrated with both sets of duration samples.
These findings are inconsistent with the possibility that the choose-short effect
reflects processes of asymmetrical- sample coding and default responding.
Marcia L. Spetch, Michael V. Mondloch, Terry W. Belke
University of Alberta
Roger Dunn
San Diego State University
Pigeons chose between 50% and 100% reinforcement on a
discrete-trials concurrent-chains procedure with fixed-ratio 1 initial links
and fixed-time terminal links. The 100% alternative always provided food after
a terminal-link delay whereas the 50% alternative provided food or blackout
equally often after a delay. Additionally, the terminal-link stimuli on the
50% alternative were correlated with the outcomes in signalled, but not in unsignalled,
conditions. The effects of intertrial interval duration and length of the terminal-link
delays on choice of the 50% alternative were investigated in four experiments.
Preference for the 50% alternative varied with signal condition and duration
of the terminal link leading to food, but not with intertrial interval or duration
of the terminal link leading to a blackout. The results are discussed in terms
of conditioned reinforcement effects, Mazur's hyperbolic decay model, and delay
reduction.
Douglas S. Grant and Marcia L. Spetch
University of Alberta
A three-phase transfer design was used to determine whether
pigeons use a single, common code to represent line and duration samples which
are associated with the same comparison stimulus. In Phase 1, two sets of samples
(two lines and two durations) were associated with either a single set of comparisons
(group MTO, many-to-one) or with different sets of comparisons (group OTO, one-to-one).
In Phase 2, one set of samples was associated with a new set of comparisons.
In Phase 3 (transfer test), the alternate set of samples was substituted for
the Phase 2 samples. Group MTO, but not group OTO, demonstrated immediate transfer.
It was concluded that associating a line and a duration sample with the same
comparison stimulus results in those samples being represented by a single code.
Marcia L. Spetch and Michael V. Mondloch
University of Alberta
Pigeons learned to peck an unmarked 2 cm square target
area, defined by 4 visually distinct graphic landmarks, on a color monitor with
an attached touch frame. The configuration of landmarks and target area was
constant during training, but their location on the screen varied across trials.
The presence, relative location, and features of the landmarks were manipulated
on probe trials. Most birds showed control by only 1 or 2 of the landmarks,
and some birds displayed surprisingly accurate search with a single landmark.
For individual birds, landmark-removal tests were very consistent with landmark-shift
tests in indicating which landmark or landmarks controlled search. However,
the dominant landmark varied across birds. Manipulation of landmark color and
shape revealed that control was based exclusively on color.
Douglas S. Grant and Marcia L. Spetch
University of Alberta
Five groups of pigeons were trained in a symbolic choice-matching task involving short (2 s) and long (10 s) durations of houselight as samples. Four groups also received training with a second set of samples: line orientations or 2- and 10-s presentations of keylight. The type of sample-to- comparison mapping varied across groups. Although only two of the five groups demonstrated a choose-short effect (a tendency to choose the comparison associated with a short sample at longer delays), all groups demonstrated temporal summation (a tendency to respond on the basis of the combined duration of two successively presented samples). Moreover, the magnitude of temporal summation was equivalent in groups which did and did not demonstrate a choose-short effect. The results suggest that the processes underlying the perception of sample duration remain invariant across different sample-to- comparison mapping arrangements, but that the memory code used to retain temporal information varies.
Marcia L. Spetch and Douglas S. Grant
University of Alberta
Pigeons were trained to discriminate between short (2
s) and long (10 s) houselight samples within successive or choice delayed matching-to-sample
tasks, and then were given four types of tests. During one type of test, the
delay interval between the sample and test period was manipulated within sessions.
Consistent with earlier findings, pigeons in the choice task displayed a reliable
choose-short tendency at longer delays, whereas those in the successive task
failed to show an analogous respond-short tendency. A second type of test entailed
multiple sample presentations: the short and long samples were preceded by short
or long presamples. Pigeons in both the choice and successive tasks showed a
temporal-summation effect rather than a sample-consistency effect. In a third
type of test, the intertrial interval was manipulated within sessions. Pigeons
in both tasks showed a respond-long bias when the intertrial interval preceding
the trial was shortened. In a final test, pigeons received no-sample tests,
and tests with a 40-s sample. Pigeons in both groups showed a strong tendency
to respond short on no-sample tests, and to respond long following a 40-s sample.
It appears that timing processes are similar in the two tasks, but that memorial
processes differ.
Douglas S. Grant and Marcia L. Spetch
University of Alberta
When trained in a symbolic choice-matching task involving
short (2-s) and long (10-s) durations as samples, pigeons tend to choose the
comparison associated with a short sample as delay increases (choose-short effect).
The present experiments showed that the choose-short effect can be eliminated
by training in many-to-one (MTO) procedures in which 2 or more sets of sample
stimuli are associated with 1 set of comparison stimuli. It is concluded that
(a) the choose-short effect results from a process of subjective shortening
that occurs during a delay if duration samples are coded analogically and (b)
samples of duration are coded nonanalogically in at least some MTO mapping arrangements.