Consistent patterns of distractor effects during decision making
- The Hong Kong Polytechnic University, Hong Kong
- University of Oxford, United Kingdom
Abstract
The value of a third potential option or distractor can alter the way in which decisions are made between two other options. Two hypotheses have received empirical support: that a high value distractor improves the accuracy with which decisions between two other options are made and that it impairs accuracy. Recently, however, it has been argued that neither observation is replicable. Inspired by neuroimaging data showing that high value distractors have different impacts on prefrontal and parietal regions, we designed a dual route decision-making model that mimics the neural signals of these regions. Here we show in the dual route model and empirical data that both enhancement and impairment effects are robust phenomena but predominate in different parts of the decision space defined by the options' and the distractor's values. However, beyond these constraints, both effects co-exist under similar conditions. Moreover, both effects are robust and observable in six experiments.
Data availability
The codes for running the mutual inhibition model, divisive normalization model, dual route model and null model can be found at:https://doi.org/10.5061/dryad.k6djh9w3cBehavioural data of Experiments 1, 3 and 7 can be found at:https://datadryad.org/stash/dataset/doi:10.5061/dryad.040h9t7Behavioural data of Experiments 2, 4-6 can be found from a link provided by Gluth and colleagues (2018) at:https://osf.io/8r4fh/Behavioural and eye tracking data of Experiment 8 can be found at:https://doi.org/10.5061/dryad.k6djh9w3c
-
Consistent patterns of distractor effects during decision makingDryad Digital Repository, 10.5061/dryad.k6djh9w3c.
-
Data from: A neural mechanism underlying failure of optimal choice with multiple alternativesDryad Digital Repository, 10.5061/dryad.040h9t7.
Article and author information
Author details
Alizée Lopez-Persem
Miriam C Klein-Flügge
Funding
Research Grants Council, University Grants Committee (25610316)
- Bolton K H Chau
Wellcome (WT100973AIA)
- Matthew F S Rushworth
Wellcome (203139/Z/16/Z)
- Matthew F S Rushworth
Medical Research Council (MR/P024955/1)
- Matthew F S Rushworth
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Ethics
Human subjects: Experiments 3, 7 and 8 were approved by ethics committee of The Hong Kong Polytechnic University and Experiment 1 was approved by that of University of Oxford.
Copyright
© 2020, Chau et al.
This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.
Metrics
-
- 1,689
- views
-
- 241
- downloads
-
- 32
- citations
Views, downloads and citations are aggregated across all versions of this paper published by eLife.
Download links
A two-part list of links to download the article, or parts of the article, in various formats.
Downloads (link to download the article as PDF)
Open citations (links to open the citations from this article in various online reference manager services)
Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)
Consistent patterns of distractor effects during decision making
eLife 9:e53850.
https://doi.org/10.7554/eLife.53850
Further reading
-
- Neuroscience
Humans and other animals often violate economic principles when choosing between multiple alternatives, but the underlying neurocognitive mechanisms remain elusive. A robust finding is that adding a third option can alter the relative preference for the original alternatives, but studies disagree on whether the third option’s value decreases or increases accuracy. To shed light on this controversy, we used and extended the paradigm of one study reporting a positive effect. However, our four experiments with 147 human participants and a reanalysis of the original data revealed that the positive effect is neither replicable nor reproducible. In contrast, our behavioral and eye-tracking results are best explained by assuming that the third option’s value captures attention and thereby impedes accuracy. We propose a computational model that accounts for the complex interplay of value, attention, and choice. Our theory explains how choice sets and environments influence the neurocognitive processes of multi-alternative decision making.
-
- Genetics and Genomics
- Neuroscience
Spinal muscular atrophy (SMA) is caused by mutations in the Survival Motor Neuron 1 (SMN1) gene. While traditionally viewed as a motor neuron disorder, there is involvement of various peripheral organs in SMA. Notably, fatty liver has been observed in SMA mouse models and SMA patients. Nevertheless, it remains unclear whether intrinsic depletion of SMN protein in the liver contributes to pathology in the peripheral or central nervous systems. To address this, we developed a mouse model with a liver-specific depletion of SMN by utilizing an Alb-Cre transgene together with one Smn2B allele and one Smn1 exon 7 allele flanked by loxP sites. Initially, we evaluated phenotypic changes in these mice at postnatal day 19 (P19), when the severe model of SMA, the Smn2B/- mice, exhibit many symptoms of the disease. The liver-specific SMN depletion does not induce motor neuron death, neuromuscular pathology or muscle atrophy, characteristics typically observed in the Smn2B/- mouse at P19. However, mild liver steatosis was observed, although no changes in liver function were detected. Notably, pancreatic alterations resembled that of Smn2B/-mice, with a decrease in insulin-producing β-cells and an increase in glucagon-producingα-cells, accompanied by a reduction in blood glucose and an increase in plasma glucagon and glucagon-like peptide (GLP-1). These changes were transient, as mice at P60 exhibited recovery of liver and pancreatic function. While the mosaic pattern of the Cre-mediated excision precludes definitive conclusions regarding the contribution of liver-specific SMN depletion to overall tissue pathology, our findings highlight an intricate connection between liver function and pancreatic abnormalities in SMA.
