36,562 research outputs found

    Stimulus & response : fieldwork in science

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    From time to time students at the faculty of Education are asked to air their views on particular educational topics which the editors propose to them. In this issue of the journal we reproduce the ideas of two students about the value of fieldwork in science.peer-reviewe

    On the assimilation of instructions : stimulus-response associations are implemented but not stimulus-task associations

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    The assimilation of instructions consists of two stages. First, a task model is formed on the basis of instructions. Second, this model is implemented, resulting in highly accessible representations, which enable reflexive behavior that guides the application of instructions. Research frequently demonstrated that instructions can lead to automatic response activation, which indicates that stimulus-response associations can be implemented on the basis of a task model. However, instructions not only indicate how to respond (stimulus-response mappings) but also when (i.e., the conditions under which mappings apply). Accordingly, we tested whether instruction implementation leads both to the activation of stimulus-response associations and of associations between stimuli and the context or task in which the instructed stimulus-response mappings are relevant (i.e., stimulus-task associations). In four experiments, we measured if implementing newly instructed stimulus-response mappings also leads to bivalence costs (i.e., shorter latencies when a stimulus can only occur in one task compared to when it can occur in two tasks), which indicate the presence of stimulus-task associations. We consistently observed automatic response activation on the basis of instructions, but no bivalence costs. A discrepancy thus exists between information conveyed in an instructed task model and the elements of that task model that are implemented. We propose that future research on automatic effects of instructions should broaden its scope and focus both on the formation of an instructed task model and its subsequent implementation

    Can Stimulus-Response Learning Theory Explain Abnormal Fixations?

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    The free energy of biomembrane and nerve excitation and the role of anesthetics

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    In the electromechanical theory of nerve stimulation, the nerve impulse consists of a traveling region of solid membrane in a liquid environment. Therefore, the free energy necessary to stimulate a pulse is directly related to the free energy difference necessary to induce a phase transition in the nerve membrane. It is a function of temperature and pressure, and it is sensitively dependent on the presence of anesthetics which lower melting transitions. We investigate the free energy difference of solid and liquid membrane phases under the influence of anesthetics. We calculate stimulus-response curves of electromechanical pulses and compare them to measured stimulus-response profiles in lobster and earthworm axons. We also compare them to stimulus-response experiments on human median nerve and frog sciatic nerve published in the literature.Comment: 10 pages, 6 figure

    Functional relations modulate the responsiveness to affordances despite the impact of conflicting stimulus-response mappings

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    The study investigated how conflicting stimulus-response mappings influenced affordance processing given a manipulation of the functional relations. Participants performed a task involving consistent-inconsistent stimulus-response mappings: Implicit Relational Assessment Procedure (IRAP). They were instructed to confirm or to deny a relation between words and tool-objects (consistent blocks) or to provide non-conventional responses (inconsistent blocks). The relations between stimuli could functionally match (e.g., Kitchen- Spatula) or not (e.g., Kitchen- Hammer), as well as the spatial relations (e.g., a match or a mismatch between participants' hand response and the tool-object orientation). The results showed faster reaction times (RTs) when functional relations between stimuli matched both in consistent and inconsistent blocks. Differences in RTs and accuracy between consistent and inconsistent blocks were only found when the functional relation between stimuli matched. No modulation of the performance was observed for mismatching functional relations and spatial relations between blocks. These results support the hypothesis that the responsiveness to affordances is strongly modulated by matching functional relations, despite the impact of conflicting stimulus-response mappings

    Computer simulation of the threshold sensitivity determinations

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    A computer simulation study was carried out to evaluate various methods for determining threshold stimulus levels for impact sensitivity tests. In addition, the influence of a number of variables (initial stimulus level, particular stimulus response curve, and increment size) on the apparent threshold values and on the corresponding population response levels was determined. Finally, a critical review of previous assumptions regarding the stimulus response curve for impact testing is presented in the light of the simulation results

    The stimulus-response crisis

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    Yarkoni correctly recognizes that one reason for psychology\u27s generalizability crisis is the failure to account for variance within experiments. We argue that this problem, and the generalizability crisis broadly, is a necessary consequence of the stimulus-response paradigm widely used in psychology research. We point to another methodology, perturbation experiments, as a remedy that is not vulnerable to the same problems

    Is automatic imitation a specialized form of stimulus–response compatibility? Dissociating imitative and spatial compatibilities

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    In recent years research on automatic imitation has received considerable attention because it represents an experimental platform for investigating a number of inter-related theories suggesting that the perception of action automatically activates corresponding motor programs. A key debate within this research centers on whether automatic imitation is any different than other long-term S-R associations, such as spatial stimulus-response compatibility. One approach to resolving this issue is to examine whether automatic imitation shows similar response characteristics as other classes of stimulus-response compatibility. This hypothesis was tested by comparing imitative and spatial compatibility effects with a two alternative forced-choice stimulus-response compatibility paradigm and two tasks: one that involved selecting a response to the stimulus (S-R) and one that involved selecting a response to the opposite stimulus (OS-R), i.e., the one not presented. The stimulus for both tasks was a left or right hand with either the index or middle finger tapping down. Speeded responses were performed with the index or middle finger of the right hand in response to the finger identity or the left-right spatial position of the fingers. Based on previous research and a connectionist model, we predicted standard compatibility effects for both spatial and imitative compatibility in the S-R task, and a reverse compatibility effect for spatial compatibility but not for imitative compatibility in the OS-R task. The results from the mean response times, mean percentage of errors, and response time distributions all converged to support these predictions. A second noteworthy result was that the recoding of the finger identity in the OS-R task required significantly more time than the recoding of the left-right spatial position, but the encoding time for the two stimuli in the S-R task was equivalent. In sum, this evidence suggests that the processing of spatial and imitative compatibility is dissociable with regard to two different processes in dual processing models of stimulus-response compatibility

    Effects of Cold Periods on the Stimulus-Response System of Phycomyces

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    The sporangiophores of Phycomyces do not exhibit phototropic responses when growth is arrested reversibly by cooling to 1°C. Unilateral UV stimuli (254 nm) applied during cold periods are stored for at least 2 hr and produce tropic responses away from the light after warm-up. During the cold period dark adaptation proceeds at a rate which decreases with the temperature
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