Precision measurement of the 5 2S1/2 - 4 2D5/2 quadrupole transition isotope shift between 88Sr+ and 86Sr+

We have measured the isotope shift of the narrow quadrupole-allowed 5 2S1/2 - 4 2D5/2 transition in 86Sr+ relative to the most abundant isotope 88Sr+. This was accomplished using high-resolution laser spectroscopy of individual trapped ions, and the measured shift is Delta-nu_meas^(88,86) = 570.281(4) MHz. We have also tested a recently developed and successful method for ab-initio calculation of isotope shifts in alkali-like atomic systems against this measurement, and our initial result of Delta-nu_calc^(88,86) = 457(28) MHz is also presented. To our knowledge, this is the first high precision measurement and calculation of that isotope shift. While the measurement and the calculation are in broad agreement, there is a clear discrepancy between them, and we believe that the specific mass shift was underestimated in our calculation. Our measurement provides a stringent test for further refinements of theoretical isotope shift calculation methods for atomic systems with a single valence electron

Laserless trapped-ion quantum simulations without spontaneous scattering using microtrap arrays

We propose an architecture and methodology for large-scale quantum simulations using hyperfine states of trapped-ions in an arbitrary-layout microtrap array with laserless interactions. An ion is trapped at each site, and the electrode structure provides for the application of single and pairwise evolution operators using only locally created microwave and radio-frequency fields. The avoidance of short-lived atomic levels during evolution effectively eliminates errors due to spontaneous scattering; this may allow scaling of quantum simulators based on trapped ions to much larger systems than currently estimated. Such a configuration may also be particularly appropriate for one-way quantum computing with trapped-ion cluster states.Comment: 12 pages, 5 figures, edited typos, added refs and text for clarification to reflect published versio

Transmission electron microscopy characterization of fluorescently labelled amyloid β 1-40 and α-synuclein aggregates

<p>Abstract</p> <p>Background</p> <p>Fluorescent tags, including small organic molecules and fluorescent proteins, enable the localization of protein molecules in biomedical research experiments. However, the use of these labels may interfere with the formation of larger-scale protein structures such as amyloid aggregates. Therefore, we investigate the effects of some commonly used fluorescent tags on the morphologies of fibrils grown from the Alzheimer's disease-associated peptide Amyloid β 1-40 (Aβ40) and the Parkinson's disease-associated protein α-synuclein (αS).</p> <p>Results</p> <p>Using transmission electron microscopy (TEM), we verify that N-terminal labeling of Aβ40 with AMCA, TAMRA, and Hilyte-Fluor 488 tags does not prevent the formation of protofibrils and amyloid fibrils of various widths. We also measure the two-photon action cross-section of Aβ40 labelled with Hilyte Fluor 488 and demonstrate that this tag is suitable for use with two-photon fluorescence techniques. Similarly, we find that Alexa Fluor 488 labelling of αS variant proteins near either the N or C terminus (position 9 or 130) does not interfere with the formation of amyloid and other types of αS fibrils. We also present TEM images of fibrils grown from αS C-terminally labelled with enhanced green fluorescent protein (EGFP). Near neutral pH, two types of αS-EGFP fibrils are observed via TEM, while denaturation of the EGFP tag leads to the formation of additional species.</p> <p>Conclusions</p> <p>We demonstrate that several small extrinsic fluorescent tags are compatible with studies of amyloid protein aggregation. However, although fibrils can be grown from αS labelled with EGFP, the conformation of the fluorescent protein tag affects the observed aggregate morphologies. Thus, our results should assist researchers with label selection and optimization of solution conditions for aggregation studies involving fluorescence techniques.</p

The Social Studies Curriculum in Atlanta Public Schools During the Desegregation Era

This historical investigation explores how teachers, students, and education officials viewed the social studies curriculum in the local context of Atlanta, and the broader state of Georgia, during the post-Civil Rights era, when integration was a court-ordered reality in the public schools. During the desegregation era, Atlanta schools were led by Atlanta Public Schools (APS) Superintendent, Dr. Alonzo Crim. Brought to Atlanta as part of a desegregation compromise, Dr. Crim became APS\u27s first African American superintendent. In particular, the authors investigate how national social studies movements, such as Man: A Course of Study (MACOS), inquiry-based learning, co-curriculum activities, and standards movements, adapted to fit this Southeastern locale, at a time when schools were struggling to desegregate. Local curriculum documents written in the 1970s reveal a traditional social studies curriculum. By the 1980s, APS\u27s social studies curriculum guides broadened to include a stronger focus on an enacted community—inside the classroom and around the world. In oral history interviews, however, former teachers, students, and school officials presented contrasting perspectives of how the social studies curriculum played out in the reality of Atlanta\u27s public schools during the desegregation era

Intercalation of 2,4-Dichlorophenoxyacetic Acid, 2-(2,4-Dichlorophenoxy)propionic Acid into Clays

This presentation was given at the AASU Research and Scholarship Symposium