scholarly journals eXpTools: A C++ class library for animation, tachistoscopic presentation, and response timing

1999 ◽  
Vol 31 (3) ◽  
pp. 387-399 ◽  
Author(s):  
C. Bruce Warner ◽  
Michael K. Martin

1995 ◽  
Vol 51 (2-3) ◽  
pp. 165-173 ◽  
Author(s):  
Helga Lejeune ◽  
Isabelle Hermans ◽  
Elisabeth Mocaër ◽  
Marie-Claire Rettori ◽  
Jean Claude Poignant ◽  
...  


1963 ◽  
Vol 12 (2) ◽  
pp. 387-398
Author(s):  
Austin Jones ◽  
Melvin Manis ◽  
Bernard Weiner

Three studies were conducted to assess the effects of subliminal reinforcements on learning. In the first two, Ss were given a discrimination task in which five geometric forms, repeated over 100 trials, were to be assigned to one of two categories. The categories were unbalanced; four geometric forms comprised one category, the remaining form the other. Response was required on each trial. Immediately after each response, the appropriate reinforcing word, “Right” or “Wrong,” was flashed at a subliminal brightness-contrast In Exp. I, under low motivation (without money incentives), Ss showed no learning of the correct discrimination, nor any evidence of probability learning with respect to relative frequency of stimulus categories. In Exp. II, the above procedure was replicated with money as the incentive. There again was no evidence of discrimination learning, i.e., acquisition of the correct response. There was, however, a significant linear trend ( p < .05) in the proportion of responses made to the more frequent stimulus category; Ss showed an increasing tendency to “match” the relative frequency of their two classes of response with the corresponding two stimulus classes. In Exp. III, Ss who were motivated by a money incentive attempted to guess whether E was thinking of an odd or an even number. Following each response, Ss were reinforced by tachistoscopic presentation of the word “Right” or “Wrong,” at time intervals which were too brief to permit recognition; half of the Ss were positively reinforced for emitting the response “Odd,” and half for the response “Even.” After 100 learning trials had been completed, the reinforcement contingencies were switched for an additional 20 trials, e.g., Ss who had been reinforced for “Odd” were now reinforced for “Even.” Ss in Exp. III showed no evidence of probability learning. Some possible explanations for the conflicting results of Exps. II and III were discussed.



1992 ◽  
Vol 35 (3) ◽  
pp. 256-267 ◽  
Author(s):  
D. J. Harper ◽  
A. D. M. Walker


Author(s):  
Roger Villela
Keyword(s):  


2019 ◽  
Vol 14 (1) ◽  
pp. 19-38 ◽  
Author(s):  
Nengzhi (Chris) Yao ◽  
Jiuchang Wei ◽  
Weiwei Zhu ◽  
Alexander Bondar

Purpose The conclusions on the importance of corporate response timing to a crisis have remained inconsistent. Some studies suggest that active response may reduce negative impacts, whereas managers argue that issuing official response frustrates stakeholders and thus decreases the firm value. The purpose of this paper is to investigate the role of external media in the response timing strategy and the consequent stock market reaction. Design/methodology/approach Based on 130 corporate crises that befell publicly listed firms in China from 2007 to 2014, this paper uses the Baidu News Search Engine and Chinese Lexical Analysis System to construct the variables of the media characteristics. A structural equation model is established to test the hypotheses. Findings The results of this paper suggest that media coverage drives response timing after a crisis. Although an official response is a burden for firms, the timing strategy has multidimensional benefits including effectively alleviating negative effects (defined as buffering effects) and repairing the market (defined as restoring effects). Moreover, the buffering effects of response timing are stronger when completeness of response is low. Originality/value This study mainly contributes to crisis communication literature by introducing the role of media in prompting managers to make timing decisions. The findings of this study provide empirical support for the importance of timing response strategy.



Author(s):  
Stephen Correia


2009 ◽  
Vol 101 (1) ◽  
pp. 474-490 ◽  
Author(s):  
Michael E. Brown ◽  
Michael Ariel

Physiological activity of the turtle cerebellar cortex (Cb), maintained in vitro, was recorded during microstimulation of inferior olive (IO). Previous single-electrode responses to such stimulation showed similar latencies across a limited region of Cb, yet those recordings lacked spatial and temporal resolution and the recording depth was variable. The topography and timing of those responses were reexamined using photodiode optical recordings. Because turtle Cb is thin and unfoliated, its entire surface can be stained by a voltage-sensitive dye and transilluminated to measure changes in its local absorbance. Microstimulation of the IO evoked widespread depolarization from the rostral to the caudal edge of the contralateral Cb. The time course of responses measured at a single photodiode matched that of single-microelectrode responses in the corresponding Cb locus. The largest and most readily evoked response was a sagittal band centered about 0.7 mm from the midline. Focal white-matter (WM) microstimulation on the ventricular surface also activated sagittal bands, whereas stimulation of adjacent granule cells evoked a radial patch of activation. In contrast, molecular-layer (ML) microstimulation evoked transverse beams of activation, centered on the rostrocaudal stimulus position, which traveled bidirectionally across the midline to the lateral edges of the Cb. A timing analysis demonstrated that both IO and WM microstimulation evoked responses with a nearly simultaneous onset along a sagittal band, whereas ML microstimulation evoked a slowly propagating wave traveling about 25 cm/s. The response similarity to IO and WM microstimulation suggests that the responses to WM microstimulation are dominated by activation of its climbing fibers. The Cb's role in the generation of precise motor control may result from these temporal and topographic differences in orthogonally oriented pathways. Optical recordings of the turtle's thin flat Cb can provide insights into that role.



2003 ◽  
pp. 227-248
Author(s):  
Stephen R. G. Fraser
Keyword(s):  


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