Evidence map›Paper›PMID 38680285›Full record

ArticleFrontiers in psychology2024

Phenotypic mismatch between suspects and fillers but not phenotypic bias increases eyewitness identifications of Black suspects.

Jennifer M Jones, Jacqueline Katzman, Margaret Bull Kovera

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Article in Frontiers in psychology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Jennifer M JonesDepartment of Psychology, The Graduate Center, City University of New York, New York, NY, United States.
Jacqueline KatzmanDepartment of Psychology, The Graduate Center, City University of New York, New York, NY, United States.
Margaret Bull KoveraDepartment of Psychology, The Graduate Center, City University of New York, New York, NY, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Despite converging evidence that people more closely associate the construct of criminality with Black people who exhibit a more African facial phenotype than Black people who express a more European phenotype, eyewitness researchers have largely ignored phenotypic bias as a potential contributor to the racial disparities in the criminal legal system. If this form of phenotypic bias extends to eyewitness identification tasks, eyewitnesses may be more likely to identify Black suspects with an African rather than European phenotype, regardless of their guilt status. Further, in cases where the witness's description of the perpetrator does not contain phenotypic information, phenotypic mismatch between the suspect and the other lineup members may bias identification decisions toward or against the suspect. If witnesses can use elements of the lineup construction to guide their identification decisions rather than relying on their recognition memory, then the lineup should be deemed unfair due to suspect bias. The current study also investigated lineup presentation method as a procedural safeguard, predicting that that when lineups were presented simultaneously, there would be a significant two-way interaction of phenotypic bias and lineup composition, with a larger simple main effect of phenotypic bias when lineups were suspect-biased (i.e., the fillers were a phenotypic mismatch to the suspect) than when all lineup members shared the same phenotype. We expected that this interaction would be significantly smaller or non-significant for sequential lineups. Methods: Participants watched a mock crime video that contained a Black culprit with either a more African phenotype or a less African phenotype before attempting identifications from a photo array that contained a suspect whose phenotype always matched the culprit viewed in the video, but varied in culprit-presence, phenotypic match of the suspect and fillers, and presentation method. Results: Participants did not identify Black suspects with Afrocentric features more often than Black suspects with Eurocentric features. However, witnesses made more identifications of suspects when the fillers did not match the suspect's phenotype compared to when all lineup members possessed similar phenotypic features. Discussion: In sum, phenotypic bias did not influence our participant-witnesses' identification decisions, nor interact with lineup composition and lineup presentation type to affect identifications of suspects, suggesting that phenotypic bias may be less influential in match-to-memory tasks than other types of legal decision-making (e.g., determining guilt and sentencing). However, the suggestiveness created by failing to match fillers' phenotypes to the suspect's phenotype can be avoided with proper attention to fair lineup construction.

Indexed as

cross-raceeyewitness identificationlineup constructionlineup fairnessown-race biasphenotypic biassuspect bias

Identifiers

PMID38680285
PMCPMC11045996

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.