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

2021 ◽  
Author(s):  
Érika Larissa Jiménez ◽  
Ana Leda Brino ◽  
Paulo Roney Kilpp Goulart ◽  
Olavo Galvão ◽  
William J. McIlvane
Keyword(s):  
Capuchin Monkeys ◽  
Simple Discrimination ◽  
Effective Use

A note on select- and reject-controlling relations in the simple discrimination of capuchin monkeys (Cebus apella)

2005 ◽  
Vol 69 (3) ◽  
pp. 295-302 ◽  
Author(s):  
Paulo R.K. Goulart ◽  
Mariana B. Mendonça ◽  
Romariz S. Barros ◽  
Olavo F. Galvão ◽  
William J. McIlvane
Keyword(s):  
Cebus Apella ◽  
Capuchin Monkeys ◽  
Simple Discrimination

Simple discrimination by exclusion in infant capuchin monkeys.

2017 ◽  
Vol 10 (1) ◽  
pp. 91-100
Author(s):  
Érika Larissa de Oliveira Jiménez ◽  
Ana Leda de Faria Brino ◽  
Paulo Roney Kilpp Goulart ◽  
Olavo de Faria Galvão
Keyword(s):  
Capuchin Monkeys ◽  
Simple Discrimination

Author response for "Sex differences in the brains of capuchin monkeys ( Sapajus [Cebus] apella )"

2020 ◽  
Author(s):  
Erin E. Hecht ◽  
Olivia T. Reilly ◽  
Marcela Benítez ◽  
Kimberley A. Phillips ◽  
Sarah Brosnan
Keyword(s):  
Sex Differences ◽  
Cebus Apella ◽  
Author Response ◽  
Capuchin Monkeys

Analysis of 3-d molecular distribution with the digital imaging microscope

1988 ◽  
Vol 46 ◽  
pp. 40-41
Author(s):  
W.A. Carrington ◽  
F.S. Fay ◽  
K.E. Fogarty ◽  
L. Lifshitz
Keyword(s):  
Image Restoration ◽  
Digital Imaging ◽  
Fluorescent Dyes ◽  
Optical Axis ◽  
Computer Hardware ◽  
Computer Algorithms ◽  
Low Contrast ◽  
Specific Proteins ◽  
Effective Use ◽  
Single Living Cells

Advances in digital imaging microscopy and in the synthesis of fluorescent dyes allow the determination of 3D distribution of specific proteins, ions, GNA or DNA in single living cells. Effective use of this technology requires a combination of optical and computer hardware and software for image restoration, feature extraction and computer graphics.The digital imaging microscope consists of a conventional epifluorescence microscope with computer controlled focus, excitation and emission wavelength and duration of excitation. Images are recorded with a cooled (-80°C) CCD. 3D images are obtained as a series of optical sections at .25 - .5 μm intervals.A conventional microscope has substantial blurring along its optical axis. Out of focus contributions to a single optical section cause low contrast and flare; details are poorly resolved along the optical axis. We have developed new computer algorithms for reversing these distortions. These image restoration techniques and scanning confocal microscopes yield significantly better images; the results from the two are comparable.

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