Factors affecting the amplitude of the feedback-related negativity during the balloon analogue risk task

Master of ScienceDepartment of Psychological SciencesMichael YoungWhen making decisions, the probability and magnitude of errors can play a major role in changing preferences. Electroencephalography (EEG) research examining the error-related negativity (ERN) and the associated feedback-related negativity (FRN) has indicated that the amplitude of each component may predict subsequent behavioral change. The current study used a version of the Balloon Analogue Risk Task (BART) that involves outcomes that are dynamically changing over time. As the balloon grows, more points are available but the probability of the balloon popping (netting zero points) is higher; the participant decides when to stop the balloon’s expansion to maximize points. The BART was adapted to facilitate the study of the FRN in dynamic environments. The purpose of Experiment 1 was to determine the effect of error magnitude on FRN amplitude during popped (incorrect) trials, whereas Experiment 2 was aimed at determining the effect of error magnitude on FRN amplitude during cashed-in (correct) trials. It was hypothesized that larger errors (i.e., the balloon popping after waiting a long time to cash-in) would result in a larger FRN than smaller errors. In Experiment 1, error magnitude did not contribute to the amplitude of the FRN. In Experiment 2, the masked points possible condition was a replication of Experiment 1. In the unmasked points possible condition, the number of points that could have been earned for each balloon was presented before participants found out how many points were earned. It was expected that there would be a larger FRN magnitude after cashed-in trials in the unmasked points possible condition compared to the masked points possible condition based on the magnitude of the error. In Experiment 2, the amplitude of the FRN was affected by the magnitude of the error on cashed-in trials in the unmasked condition, but not the masked condition. These results are seemingly at odds, and cannot be assimilated into any currently extant model of the FRN. An explanation relying on the motivational importance of errors is discussed

The James Webb Space Telescope Mission

Twenty-six years ago a small committee report, building on earlier studies, expounded a compelling and poetic vision for the future of astronomy, calling for an infrared-optimized space telescope with an aperture of at least $4m$. With the support of their governments in the US, Europe, and Canada, 20,000 people realized that vision as the $6.5m$ James Webb Space Telescope. A generation of astronomers will celebrate their accomplishments for the life of the mission, potentially as long as 20 years, and beyond. This report and the scientific discoveries that follow are extended thank-you notes to the 20,000 team members. The telescope is working perfectly, with much better image quality than expected. In this and accompanying papers, we give a brief history, describe the observatory, outline its objectives and current observing program, and discuss the inventions and people who made it possible. We cite detailed reports on the design and the measured performance on orbit.Comment: Accepted by PASP for the special issue on The James Webb Space Telescope Overview, 29 pages, 4 figure

IL-4Ralpha-associated antigen processing by B cells promotes immunity in Nippostrongylus brasiliensis infection.

In this study, B cell function in protective T(H)2 immunity against N. brasiliensis infection was investigated. Protection against secondary infection depended on IL-4Ralpha and IL-13; but not IL-4. Protection did not associate with parasite specific antibody responses. Re-infection of B cell-specific IL-4Ralpha(-)/(-) mice resulted in increased worm burdens compared to control mice, despite their equivalent capacity to control primary infection. Impaired protection correlated with reduced lymphocyte IL-13 production and B cell MHC class II and CD86 surface expression. Adoptive transfer of in vivo N. brasiliensis primed IL-4Ralpha expressing B cells into naive BALB/c mice, but not IL-4Ralpha or IL-13 deficient B cells, conferred protection against primary N. brasiliensis infection. This protection required MHC class II compatibility on B cells suggesting cognate interactions by B cells with CD4(+) T cells were important to co-ordinate immunity. Furthermore, the rapid nature of these protective effects by B cells suggested non-BCR mediated mechanisms, such as via Toll Like Receptors, was involved, and this was supported by transfer experiments using antigen pulsed Myd88(-)/(-) B cells. These data suggest TLR dependent antigen processing by IL-4Ralpha-responsive B cells producing IL-13 contribute significantly to CD4(+) T cell-mediated protective immunity against N. brasiliensis infection