Interactive Documents based on Discrete Trials

Author(s):  
Alex F. Orlando ◽  
Isabela Zaine ◽  
Maria G. Pimentel ◽  
Deisy G. De Souza ◽  
Cesar A.C. Teixeira
Keyword(s):  
1997 ◽  
Vol 133 (3) ◽  
pp. 269-274 ◽  
Author(s):  
W. L. Woolverton ◽  
Justin A. English ◽  
Michael R. Weed

2006 ◽  
Vol 185 (2) ◽  
pp. 150-159 ◽  
Author(s):  
Sara J. Ward ◽  
Christopher Läck ◽  
Drake Morgan ◽  
David C. S. Roberts

2014 ◽  
Vol 47 (4) ◽  
pp. 765-776 ◽  
Author(s):  
Joy S. Pollard ◽  
Thomas S. Higbee ◽  
Jessica S. Akers ◽  
Matthew T. Brodhead

2012 ◽  
Vol 6 (4) ◽  
pp. 1321-1330 ◽  
Author(s):  
Kristen L. Young ◽  
Ashley L. Boris ◽  
Kendra M. Thomson ◽  
Garry L. Martin ◽  
C.T. Yu

1988 ◽  
Vol 43 (6) ◽  
pp. 747-753 ◽  
Author(s):  
Jose Mama Cales ◽  
Santiago Segovia ◽  
Paloma Enríquez ◽  
Antonio Guillamón

1963 ◽  
Vol 12 (2) ◽  
pp. 385-386
Author(s):  
John W. Davenport

An apparatus consisting of a straight alley encircled by a revolving ring of cubicles was described. This provided a method which was successful in speeding up the administration of discrete trials in simple approach learning of rats and in minimizing between-trial handling of Ss.


1977 ◽  
Vol 55 (1) ◽  
pp. 121-125 ◽  
Author(s):  
Roger Stretch ◽  
Gary J. Gerber

Responding for intravenous injections of morphine was studied using a discrete-trials procedure in squirrel monkeys. For one group, each session consisted of 10 trials at an inter-trial interval of 15 min; for the second group, each session consisted of 100 trials at an inter-trial interval of 1.5 min. When different injection doses of morphine (1–1000 μg/kg per injection), including saline as a control procedure, were substituted at random for blocks of five consecutive sessions, the frequency of morphine self-administration was found to be an inverted U-shaped function of the injection dose. This relationship was observed in each group of monkeys, despite a 10-fold difference in the total amount of the drug which was available for self-administration per session when a given injection dose was substituted for both groups. The results show that the injection dose of morphine acted as a primary determinant of response probability, even under circumstances in which trial spacing imposed a significant delay between consecutive opportunities for drug self-administration.


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