Suchergebnisse

T. 1. - 1857. - XVI,336 S.; T. 2. - 1857. - 624 S.; T. 3. - 1859. - 517 S.; T. 4. - 1860. - 540 S

The present study investigates how attendees at national celebratory crowd events-specifically St. Patrick's Day parades-understand the role of such events in representing and uniting the national community. We conducted semi-structured interviews with people who attended St. Patrick's Day parades in either Dublin or Belfast. In year 1, full-length interviews were conducted before and after the events (N=17), and in years 1 and 2, shorter interviews were conducted during the events (year 1 N=170; year 2 N=142). Interview data were analysed using thematic analysis, allowing the identification of three broad themes. Participants reported that (i) the events extend the boundary of the national group, using participation to define who counts as Irish; (ii) the events strategically represent the nature of the national group, maximising positive images and managing stereotypical representations; and (iii) symbolism serves to unify the group but can also disrupt already fragile unity and so must be managed. Overall, this points to a strategic identity dimension to these crowd events. We discuss the implications of these findings for future research in terms of the role of large-scale celebratory events in the strategic representation of everyday social identities.

AbstractThis work presents a combined optical and magneto‐optical spectroscopic study of thulium iron garnet (Tm3Fe5O12, TmIG) films on substituted gadolinium gallium garnet (Gd2.6Ca0.4Ga4.1Mg0.25Zr0.65O12, sGGG) substrates. Spectroscopic ellipsometry, transmission spectroscopy, magneto‐optical Kerr effect spectroscopy and Raman spectroscopy results are presented for TmIG films with a thickness in the range from 20 to 300 nm grown on sGGG by pulsed laser deposition. The complex dielectric functions of TmIG and sGGG are determined and compared with previously published results for bulk yttrium iron garnet and GGG, respectively. The magneto‐optical spectroscopy corroborated with Raman spectroscopy sheds light on strain‐induced changes as a function of TmIG film thickness.