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Movement Cues Aid Face Recognition in Developmental Prosopagnosia
No full textObjective: Seeing a face in motion can improve face recognition in the general population, and studies of face matching indicate that people with face recognition difficulties (developmental prosopagnosia; DP) may be able to use movement cues as a supplementary strategy to help them process faces. However, the use of facial movement cues in DP has not been examined in the context of familiar face recognition. This study examined whether people with DP were better at recognising famous faces presented in motion, compared to static. Methods: Nine participants with DP and 14 age-matched controls completed a famous face recognition task. Each face was presented twice across two blocks: once in motion and once as a still image. Discriminability (A’) was calculated for each block. Results: Participants with DP showed a significant movement advantage overall. This was driven by a movement advantage in the first block, but not in the second block. Participants with DP were significantly worse than controls at identifying faces from static images, but there was no difference between DPs and controls for moving images. Conclusions: Seeing a familiar face in motion can improve face recognition in people with DP, at least in some circumstances. The mechanisms behind this effect are unclear, but these results suggest that some people with DP are able to learn and recognise patterns of facial motion, and movement can act as a useful cue when face recognition is impaired
Erratum: ``Timing of Five Millisecond Pulsars Discovered in the PALFA Survey'' (2015, ApJ, 800, 123)
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The very worst sites of filth and darkness.’ Exploring the evolving Industrial community of Angel Meadow
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Biodegradation of carbon nanohorns in macrophage cells.
No full textWith the rapid developments in the medical applications of carbon nanomaterials such as carbon nanohorns (CNHs), carbon nanotubes, and graphene based nanomaterials, understanding the long-term fate, health impact, excretion, and degradation of these materials has become crucial. Herein, the in vitro biodegradation of CNHs was determined using a non-cellular enzymatic oxidation method and two types of macrophage cell lines. Approximately 60% of the CNHs was degraded within 24 h in a phosphate buffer solution containing myeloperoxidase. Furthermore, approximately 30% of the CNHs was degraded by both RAW 264.7 and THP-1 macrophage cells within 9 days. Inflammation markers such as pro-inflammatory cytokines interleukin 6 and tumor necrosis factor α were not induced by exposure to CNHs. However, reactive oxygen species were generated by the macrophage cells after uptake of CNHs, suggesting that these species were actively involved in the degradation of the nanomaterials rather than in an inflammatory pathway induction
2D and 3D imaging of fatigue failure mechanisms of 3D woven composites
No full textA detailed investigation of the failure mechanisms for angle-interlocked (AI) and modified layer-to-layer (MLL) three dimensional (3D) woven composites under tension–tension (T–T) fatigue loading has been conducted using surface optical microscopy, cross-sectional SEM imaging, and non-destructive X-ray computed tomography (CT). X-ray microCT has revealed how cracks including surface matrix cracks, transverse matrix cracks, fibre/matrix interfacial debonding or delamination develop, and has delineated the complex 3D morphology of these cracks in relation to fibre architecture. For both weaves examined, transverse cracks soon become uniformly distributed in the weft yarns. A higher crack density was found in the AI composite than the MLL composite. Transverse cracking initiates in the fibre rich regions of weft yarns rather than the resin rich regions. Delaminations in the failed MLL specimen were more extensive than the AI specimen. It is suggested that for the MLL composite that debonding between the binder yarns and surrounding material is the predominant damage mechanism