Synchronizing programs using Macromedia Director plug-ins: An example from the field of developmental psychopathology

Synchronizing the display of a stimulus with physiological recording or subjects’ behavioral responses is crucial for acquiring valid measures of performance. This article describes a technique for integrating the presentation of stimuli, behavior reports, and physiological data employing Macromedia Director and a standard biometric program using an example from the field of developmental psychopathology. Our experience has been that the use of this technique is effective in creating complex protocols for research. Although the temporal accuracy available from this particular method is adequate for some experiments, it is not suited for investigations requiring single millisecond accuracy. Considerations and suggestions for utilizing this and similar techniques for integrating data collection and stimuli presentation are discussed.     

Control by reinforcers across time and space: A review of recent choice research

Reinforcers affect behavior. A fundamental assumption has been that reinforcers strengthen the behavior they follow, and that this strengthening may be context‐specific (stimulus control). Less frequently discussed, but just as evident, is the observation that reinforcers have discriminative properties that also guide behavior. We review findings from recent research that approaches choice using nontraditional procedures, with a particular focus on how choice is affected by reinforcers, by time since reinforcers, and by recent sequences of reinforcers. We also discuss how conclusions about these results are impacted by the choice of measurement level and display. Clearly, reinforcers as traditionally considered are conditionally phylogenetically important to animals. However, their effects on behavior may be solely discriminative, and contingent reinforcers may not strengthen behavior. Rather, phylogenetically important stimuli constitute a part of a correlated compound stimulus context consisting of stimuli arising from the organism, from behavior, and from physiologically detected environmental stimuli. Thus, the three‐term contingency may be seen, along with organismic state, as a correlation of stimuli. We suggest that organisms may be seen as natural stimulus‐correlation detectors so that behavioral change affects the overall correlation and directs the organism toward currently appetitive goals and away from potential aversive goals. As a general conclusion, both historical and recent choice research supports the idea that stimulus control, not reinforcer control, may be fundamental.     

An automated regional taste-testing system

A fully programmable and portable automated regional taste-testing system is described. This system utilizes a glass stimulator held to the surface of the tongue by a mild vacuum. Temporally and spatially discrete trains of stimuli, delivered from a bank of glass reservoirs through microprocessor-controlled Teflon solenoid valves and both glass and Tygon tubing, can be delivered to the lingual surface at millisecond durations. Rinses between stimuli are similarly programmed. The stimulus delivery is monitored at the surface of the tongue, using a capacitance sensor to alert the subject of stimulus delivery. An example of the application of this system is shown, in which we demonstrate that the detection threshold for NaCl is inversely related to stimulus duration by a power function.     

Effective use of the blank comparison procedure in simple discrimination by infant capuchin monkeys: A methodological note

In studies of simple and conditional discrimination, procedures are needed to measure those aspects of stimuli that control behavior. The blank comparison procedure is one such procedure. It was designed explicitly for assessing S+ and S- functions when discriminative stimuli are presented simultaneously. In this procedure, a neutral stimulus serves sometimes as S+ and sometimes as S-. Its discriminative function is defined in relation to other stimuli in the display. The present study aimed to prepare 2 infant female capuchin monkeys for the effective use of the blank comparison procedure in a simple discrimination task. First, simple discrimination training was applied up to a stable accuracy criterion of ≥90%. This training was followed by the replacement of S+ and then of S- stimuli with new stimuli. Ultimately, trials with the blank comparison were introduced. Following this sequence, both monkeys immediately displayed highly accurate blank-comparison performances without the need for stimulus control shaping or other preparatory discrimination training. Thus, this procedure sequence may be an efficient, effective method for establishing blank-comparison baselines for experimental analyses of S+/S- discriminative functions and perhaps for other applications in teaching simple and conditional discrimination performances to this species and others.     

The phenomenology of spatial integration: data and models

A briefly presented visual stimulus followed by darkness seems to persist beyond its physical offset. We are concerned here with the relation between two characteristics of this visible persistence: first, its phenomenological resemblance to the stimulus that spawned it and second, its usefulness as a basis for integrating visual stimuli that are separated in time. We describe two experiments using a task in which two halves of a visual stimulus were presented successively and observers reported how complete the stimulus appeared to be. Stimuli appeared less complete with increases in both the duration of the interval intervening between presentation of the two halves and the duration of the initially presented stimulus half. This data pattern is similar to that obtained in tasks in which spatial integration of two temporally disparate stimuli is necessary for correct responding. On the basis of this similarity, we argue that phenomenological appearance and ability to integrate stimuli over time are two facets of the same perceptual events. We describe a formal model to account for these and other data.     

A simple and sensitive method to measure timing accuracy

Timing accuracy in presenting experimental stimuli (visual information on a PC or on a TV) and responding (keyboard presses and mouse signals) is of importance in several experimental paradigms. In this article, a simple system for measuring timing accuracy is described. The system uses two PCs (at least Pentium II, 200 MHz), a photocell, and an amplifier. No additional boards and timing hardware are needed. The first PC, a SlavePC, monitors the keyboard presses or mouse signals from the PC under test and uses a photocell that is placed in front of the screen to detect the appearance of visual stimuli on the display. The software consists of a small program running on the SlavePC. The SlavePC is connected through a serial line with a second PC. This MasterPC controls the SlavePC through an ActiveX control, which is used in a Visual Basic program. The accuracy of our system was investigated by using a similar setup of a SlavePC and a MasterPC to generate pulses and by using a pulse generator card. These tests revealed that our system has a 0.01-msec accuracy. As an illustration, the reaction time accuracy of INQUISIT for a few applications was tested using our system. It was found that in those applications that we investigated, INQUISIT measures reaction times from keyboard presses with millisecond accuracy.     

MIDI and Macintosh: Searching for a better mousetrap

This paper will explore how MIDI (musical instrument digital interface)-technology can benefit researchers interested in using Apple Macintosh computers for stimulus control and response timing. One example presented here will illustrate how MIDI equipment can be adapted to provide millisecond precision response timing that cannot be obtained with solely software-based timing techniques. Another example will show how to use MIDI to control sound-generating devices that far surpass the sound-producing capabilities built into the Macintosh. There will also be a discussion of how certain MIDI equipment can provide information on the velocity and the duration of a response that is not available with traditional laboratory hardware. The examples presented here rely on a commercial software library called MIDIBASIC that was designed to be used with Microsoft QuickBasic. The availability of a millisecond timer that can be called from QuickBasic may offer a special advantage for researchers who have previously written programs in an Apple II environment using AppleSoft Basic.     

Algorithms and selective attention

Selective attention is hypothesized to be controlled by intentionally chosen algorithms that specify how stimuli are to be processed. These experiments attempted to measure the time to select such algorithms. Subjects were given a two-choice reaction time task with a variety of different possible stimuli. Prior to each trial, subjects viewed a cue under their control that indicated the two possible stimuli for the upcoming trial. During this interval, subjects presumably selected a stimulus identification algorithm appropriate for that pair of letters; the duration of the interval was used as an index of algorithm selection time. The results indicated that selection time increases with the number of alternative algorithms and that algorithms may consist, in part, of perceptual tests to determine which of the two possible stimuli was presented. A specific model of the selection process was proposed to account for the results.     

Effect of visual-verbal load and spatial compatibility on stimulus response

This study examined the effects of visual-verbalload (as measured by a visually presented reading-memory task with three levels) on a visual/auditory stimulus-response task. The three levels of load were defined as follows: "No Load" meant no other stimuli were presented concurrently; "Free Load" meant that a letter (A, B, C, or D) appeared at the same time as the visual or auditory stimulus; and "Force Load" was the same as "Free Load," but the participants were also instructed to count how many times the letter A appeared. The stimulus-response task also had three levels: "irrelevant," "compatible," and "incompatible" spatial conditions. These required different key-pressing responses. The visual stimulus was a red ball presented either to the left or to the right of the display screen, and the auditory stimulus was a tone delivered from a position similar to that of the visual stimulus. Participants also processed an irrelevant stimulus. The results indicated that participants perceived auditory stimuli earlier than visual stimuli and reacted faster under stimulus-response compatible conditions. These results held even under a high visual-verbal load. These findings suggest the following guidelines for systems used in driving: an auditory source, appropriately compatible signal and manual-response positions, and a visually simplified background.     

Attending to the distractor and old/new discriminations in negative priming

When participants ignore an irrelevant distractor they typically show impaired responding to that item if it becomes the relevant stimulus on a subsequent trial. In Experiment 1 (N = 64), a masked white colour name was presented briefly before a Stroop display. Negative priming in colour naming occurred when the colour of the lettering for the Stroop stimulus matched the colour name displayed in the first display, consistent with the proposal of temporal discrimination theory that negative priming arises because a recurrence of an unattended stimulus cannot readily be classified as old or new. Experiment 2 (N = 32) replicated negative priming in the interleaved-word display where participants had to name the red word from a pair of red and green words. In Experiment 3 (N = 32) and Experiment 4 (N = 28) the participants were required to attend to but not respond to the words in the prime display and name one of two interleaved words in the probe display. Negative priming was observed in this arrangement, consistent with the episodic retrieval theory of negative priming. The temporal discrimination model may need to be extended to situations in which the attended stimuli have different responses attached to them.     

A computer-controlled cardiotachometer

A versatile display system for presenting heart rate information is described. The display has a table with 10 rows and 50 columns. This 10 by 50 matrix contains all integers from 0 to 499, so that it can display the instantaneous R-R intervals of a rat’s EKG to the nearest millisecond. At each beat 1 of 10 vertically and 1 of 50 horizontally arranged indicator lights are turned on to provide the coordinates for reading the table. Either beat-to-beat or averaged heart rate or period is displayed. Small and large changes can be easily and accurately observed on the same scale. The lights are controlled by a PDP-8/e. A listing of the assembler program is presented.     

The discrimination of relative frequency by pigeons.

Five experiments addressed the issue of how pigeons learn to discriminate the relative frequency of stimuli. During a sampling period, three different stimuli (keylights) were presented serially, in mixed order, and with different frequencies. During a choice period, the stimuli were presented simultaneously, and reinforcement was arranged for choosing the stimulus that was presented the least number of times during the sample. The results showed that (a) the overall proportion of correct choices was always above chance levels; (b) the likelihood of a correct choice decreased with the serial position of the correct stimulus, a negative recency effect; (c) when the last three stimuli of the sample were constrained to be one of each kind, the negative recency effect decreased but errors became more likely when the correct stimulus occurred early in the sample, a negative primacy effect; (d) accurate performance generalized to new and larger samples; and (e) under some conditions the probability of a correct choice was independent of the serial position of the correct stimulus. The serial position curves suggest that in a least frequent discrimination task, two processes determine how the least frequent stimulus controls behavior: a passive decay process (the stimulus loses its effectiveness with time since its last occurrence), and a residual salience process (when the stimulus occurs in the first position it may decay to a higher asymptote than when it occurs in later positions.     

Stimulus-specific processing consequences of pattern goodness

Two issues concerning the effects of visual pattern goodness on information processing time were investigated: the role of memory vs. encoding and the role of individual stimulus goodness vs. stimulus similarity. A sequential “same-different” task was used to provide differentiation of target item or memory effects from display item or encoding effects. Experiment 1 used four alternative stimuli in each block of trials. The results showed that good patterns were processed faster than poor patterns for both “same” and “different” responses. Furthermore, the goodness of the target item had a greater effect on reaction time than did the goodness of the display item, indicating that memory is more important than encoding in producing faster processing of good stimuli. Effects of interstimulus similarity on processing time were minimal, although isolation of good stimuli in a similarity space could explain many of the results. Experiment 2 replicated the results of Experiment 1, despite the fact that differences in similarity space had been minimized by using only two alternative stimuli in each block. In addition, the speed of processing a “same” pair was essentially independent of the particular alternative stimulus in a block. These results suggest that in this task, there is a processing advantage for good stimuli that is stimulus specific, with the effect operating primarily in memory.     

Direct measurement of the system latency of gaze-contingent displays

Gaze-contingent displays combine a display device with an eyetracking system to rapidly update an image on the basis of the measured eye position. All such systems have a delay, the system latency, between a change in gaze location and the related change in the display. The system latency is the result of the delays contributed by the eyetracker, the display computer, and the display, and it is affected by the properties of each component, which may include variability. We present a direct, simple, and low-cost method to measure the system latency. The technique uses a device to briefly blind the eyetracker system (e.g., for video-based eyetrackers, a device with infrared light-emitting diodes (LED)), creating an eyetracker event that triggers a change to the display monitor. The time between these two events, as captured by a relatively low-cost consumer camera with high-speed video capability (1,000 Hz), is an accurate measurement of the system latency. With multiple measurements, the distribution of system latencies can be characterized. The same approach can be used to synchronize the eye position time series and a video recording of the visual stimuli that would be displayed in a particular gaze-contingent experiment. We present system latency assessments for several popular types of displays and discuss what values are acceptable for different applications, as well as how system latencies might be improved.     

Timing and reaction time.

Because reaction time (RT) tasks are generally repetitive and temporally regular, participants may use timing strategies that affect response speed and accuracy. This hypothesis was tested in 3 serial choice RT experiments in which participants were presented with stimuli that sometimes arrived earlier or later than normal. RTs increased and errors decreased when stimuli came earlier than normal, and RTs decreased and errors increased when stimuli came later than normal. The results were consistent with an elaboration of R. Ratcliff's diffusion model (R. Ratcliff, 1978; R. Ratcliff & J. N. Rouder, 1998; R. Ratcliff, T. Van Zandt, & G. McKoon, 1999), supplemented by a hypothesis developed by D. Laming (1979a, 1979b), according to which participants initiate stimulus sampling before the onset of the stimulus at a time governed by an internal timekeeper. The success of this model suggests that timing is used in the service of decision making.     

The flanker effect does not reflect the processing of “task-irrelevant” stimuli: Evidence from inattentional blindness

It is often the case that stimuli (or aspects of a stimulus) are referred to as being “task-irrelevant.” Here, we recount where this label originated and argue that the use of this label is at odds with the concept of “relevance” that has arisen in the contingent-capture literature. This is not merely a matter of labels, but a matter of inference: When people describe a flanker stimulus as being “task-irrelevant,” they may be (and sometimes are) tempted to infer that the conditions that were studied in the flanker task generalize to other tasks and other types of stimuli. Here, we show that this generalization is not warranted. The flanker effect exists not because attention has failed at selecting only the target from the display, but rather, the effect arises precisely because attention succeeded at selecting target-like (i.e., attentionally relevant) stimuli from the display. As a result, the flanker effect should not be used to infer how stimuli that are entirely unrelated to a participant’s main task would be processed. We propose the use of a new terminology to replace this potentially misleading label.     

材料生态性和性别因素对理解友好与敌对意图的影响

为考察材料生态性、被试性别和角色性别对理解友好与敌对意图的影响,分析了100名被试观察由2名男性或2名女性表演的三类互动意图的照片或卡通时的正确率和反应时。结果：理解真实人物的正确率高于虚拟角色;女性被试理解虚拟角色的反应时长于真实人物,而男性被试却未出现材料生态性差异;理解男性角色敌对意图的反应时短于女性角色的,而理解友好意图时却未出现角色性别差异。研究为负性偏向等理论提供实证证据,揭示材料生态性、角色性别对理解友好和敌对意图的影响机制。