Stable individual differences in unfamiliar face identification: Evidence from simultaneous and sequential matching tasks.

Matching identity in images of unfamiliar faces is difficult: Images of the same person can look different and images of different people can look similar. Recent studies have capitalized on individual differences in the ability to distinguish match (same ID) vs. mismatch (different IDs) face pairs to inform models of face recognition. We addressed two significant gaps in the literature by examining the stability of individual differences in both sensitivity to identity and response bias. In Study 1, 210 participants completed a battery of four tasks in each of two sessions separated by one week. Tasks varied in protocol (same/different, lineup, sorting) and stimulus characteristics (low vs. high within-person variability in appearance). In Study 2, 148 participants completed a battery of three tasks in a single session. Stimuli were presented simultaneously on some trials and sequentially on others, introducing short-term memory demands. Principal components analysis revealed two components that were stable across time and tasks: sensitivity to identity and bias. Analyses of response times suggest that individual differences in bias reflect decision-making processes. We discuss the implications of our findings in applied settings and for models of face recognition.

Evaluation of equine oocyte developmental competence using polarized light microscopy.

The purpose of this study was to observe in vitro-matured equine oocytes with an objective computerized technique that involves the use of a polarized light microscope (PLM) in addition to the subjective morphological evaluation obtained using a classic light microscope (LM). Equine cumulus-oocyte complexes (COCs, n = 922) were subjected to different in vitro maturation times (24, 36 or 45 h), however, only 36-h matured oocytes were analyzed using CLM. The 36-h matured oocytes that reached maturity were parthenogenetically activated to evaluate the quality and meiotic competence. Average maturation percentages per session in groups 1, 2 and 3 (24-, 36- and 45-h matured oocytes respectively) were 29.31 ± 13.85, 47.01 ± 9.90 and 36.62 ± 5.28%, whereas the average percentages of immature oocytes per session were 28.78 ± 20.17, 7.83 ± 5.51 and 22.36 ± 8.39% respectively. The zona pellucida (ZP) birefringent properties were estimated and correlated with activation outcome. ZP thickness and retardance of the inner layer of the zona pellucida (IL-ZP) were significantly increased in immature oocytes compared with mature oocytes (P < 0.001 and P < 0.01 respectively). The comparison between parthenogenetically activated and non-activated oocytes showed a significant increase in the area and thickness of the IL-ZP in parthenogenetically activated oocytes (P < 0.01). These results show that the 36-h in vitro maturation (IVM) protocol allowed equine oocytes to reach maturity, and PLM observation of ZP can be used to distinguish mature and immature oocytes as well as activated and non-activated oocytes.