Related Experiment Video
Updated: Jun 16, 2026

Measuring Attention and Visual Processing Speed by Model-based Analysis of Temporal-order Judgments
Published on: January 23, 2017
The Wertheimer-Benary effect does not invert, and a nulled Wertheimer-Benary effect
Abigail E Huang1, Sanchita Ghosh, Alice J Hon
1New Jersey Medical School, University of Medicine & Dentistry of New Jersey, Newark, NJ 07103, USA.
Abstract:
More than three-quarters of a century ago Wertheimer and Benary demonstrated an ingenious and clear, though, interestingly, small effect: a grey triangle just inside an arm of a black cross on a white background appears slightly lighter than an identical triangle immediately adjacent to the cross, despite both triangles having the same perimeter exposure to black and white. Over a generation ago White discovered an apparently related, but far stronger effect: when short grey (test) bars are placed onto either black or white alternating long bars, the short test bars placed on the long black bars appear much lighter than those placed on the long white bars. A decade ago Spehar, Gilchrist, and Arend found that, enigmatically, if the short test bars in White's effect are the lightest stimulus in a figure, then the relative lightness of the test bars inverts compared with the standard version of White's effect. Here we show that the Wertheimer-Benary effect does not invert, but instead produces a very weak version of the standard effect. We also demonstrate a novel, nulled Wertheimer-Benary effect.
More Related Videos
Related Concept Videos
Nuclear Overhauser Enhancement (NOE)
Sign Test for Matched Pairs
To conduct the sign test, we first calculate the differences in value between...
Two-Way ANOVA
The two-way ANOVA analysis initially begins by stating the null hypothesis that there is an interaction effect between the two factors of a dataset. This effect can be visualized using line segments formed by joining the means for...
¹H NMR Chemical Shift Equivalence: Enantiotopic and Diastereotopic Protons
In chiral compounds such as 2-butanol, replacing the methylene hydrogens at C3 produces a pair of...
SN1 Reaction: Stereochemistry
In the first step of an SN1 reaction, the bond between the electrophilic carbon and the leaving group ionizes to generate the carbocation intermediate. The second step of the mechanism is the nucleophilic attack.
In the formed carbocation, the positively charged carbon is sp2 hybridized with a trigonal planar geometry. As all the three substituents lie on the same plane, a plane of symmetry for the...
Wald-Wolfowitz Runs Test I
The test works...

