On wind-driven electrojets at magnetic cusps in the nightside ionosphere of Mars

Mars has a complex magnetic topology where crustal magnetic fields can interact with the solar wind magnetic field to form magnetic cusps. On the nightside, solar wind electron precipitation can produce enhanced ionization at cusps while closed field regions adjacent to cusps can be devoid of significant ionization. Using an electron transport model, we calculate the spatial structure of the nightside ionosphere of Mars using Mars Global Surveyor electron measurements as input. We find that localized regions of enhanced ionospheric density can occur at magnetic cusps adjacent to low density regions. Under this configuration, thermospheric winds can drive ionospheric electrojets. Collisional ions move in the direction of the neutral winds while magnetized electrons move perpendicular to the wind direction. This difference in motion drives currents and can lead to charge accumulation at the edges of regions of enhanced ionization. Polarization fields drive secondary currents which can reinforce the primary currents leading to electrojet formation. We estimate the magnitude of these electrojets and show that their magnetic perturbations can be detectable from both orbiting spacecraft and the surface. The magnitude of the electrojets can vary on diurnal and annual time scales as the strength and direction of the winds vary. These electrojets may lead to localized Joule heating, and closure of these currents may require field-aligned currents which may play a role in high altitude acceleration processes

On the origin of aurorae on Mars

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/95268/1/grl20829.pd

Model calculations of electron precipitation induced ionization patches on the nightside of Mars

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/94812/1/grl23162.pd

Long-term effects of tongue piercing — a case control study

The aim of this study was to evaluate tooth and periodontal damage in subjects wearing a tongue piercing (TP) in comparison to matched control subjects without tongue piercing. Members of the German Federal Armed Forces who had TP (group TP) and a matched control group (group C) volunteered to take part in the study. The time in situ, localization and material of TP were documented. Dental examinations included DMF-T, oral hygiene, enamel fissures (EF), enamel cracks (EC) and recessions. Statistical analysis was determined by χ2 test and the t test. Both groups had 46 male subjects (mean age 22.1 years). The piercings had been in situ for 3.8 ± 3.1 years. Subjects in the TP group had a total of 1,260 teeth. Twenty-nine subjects had 115 teeth (9.1%) with EF (67% lingual). In group C (1,243 teeth), 30 subjects had 60 teeth with EF (4.8%, 78% vestibular) (p < 0.01). Thirty-eight subjects belonging to group TP had EC in 186 teeth (15%). In group C, 26 subjects with 56 teeth (4.5%) were affected by EC (p < 0.001). Twenty-seven subjects in group TP had 97 teeth (7.7%) with recessions. Lingual surfaces of anterior teeth in the lower jaw were affected most frequently (74%). In group C, 8 subjects had 19 teeth (1.5%) with recessions (65% vestibular). Differences between the two groups were statistically significant (p < 0.001). Tongue piercing is correlated with an increased occurrence of enamel fissures, enamel cracks and lingual recessions. Patients need better information on the potential complications associated with tongue piercing

18th IEEE Real-Time Systems Symposium: Work in Progress Sessions

Dear Colleagues: Following, the success of last year's Work In Progress (WIP) Sessions during RTSS'96, I am pleased to continue that tradition by presenting you 10 excellent WIP reports for RTSS'97. The prime purpose of RTSS WIP sessions is to provide researchers in Academia and Industry an opportunity to discuss their evolving ideas and gather feedback thereon from the real-time community at large. There were 16 submissions for WIP presentations, of which 10 have been accepted for presentation during the symposium and for inclusion in RTSS'97 WIP proceedings. If you would like to reference any article included in the RTSS'97 WIP Proceedings, please note that theses proceedings are published as a Technical Report from Boston University, Computer Science Department (BUCS-TR-97- 021). Many people worked hard to make the idea of holding the WIP sessions a reality. In particular, I would like to thank Kwei-Jay Lin for accommodating the WIP sessions within the busy schedule of RTSS'97. Also, I would like to thank all members of the RTSS'97 Program Committee who helped me review these submissions. Finally, I would like to thank all those who submitted their work to RTSS'97 WIP Sessions. I hope these sessions will prove beneficial, both to the WIP presenters and to RTSS'97 attendees. Azer Bestavros RTSS'97 WIP Chair December 1997.IEEE-CS TC-RT

Gold Nanoparticle-Based Surface-Enhanced Raman Scattering for Noninvasive Molecular Probing of Embryonic Stem Cell Differentiation

This study reports the use of gold nanoparticle-based surface-enhanced Raman scattering (SERS) for probing the differentiation of mouse embryonic stem (mES) cells, including undifferentiated single cells, embryoid bodies (EBs), and terminally differentiated cardiomyocytes. Gold nanoparticles (GNPs) were successfully delivered into all 3 mES cell differentiation stages without affecting cell viability or proliferation. Transmission electron microscopy (TEM) confirmed the localization of GNPs inside the following cell organelles: mitochondria, secondary lysosome, and endoplasmic reticulum. Using bright- and dark-field imaging, the bright scattering of GNPs and nanoaggregates in all 3 ES cell differentiation stages could be visualized. EB (an early differentiation stage) and terminally differentiated cardiomyocytes both showed SERS peaks specific to metabolic activity in the mitochondria and to protein translation (amide I, amide II, and amide III peaks). These peaks have been rarely identified in undifferentiated single ES cells. Spatiotemporal changes observed in the SERS spectra from terminally differentiated cardiomyocyte tissues revealed local and dynamic molecular interactions as well as transformations during ES cell differentiation