Paleomagnetism of a Paleozoic anorthosite from the Appalachian Piedmont, northern Delaware: possible tectonic implications

Two components of magnetization have been observed in fourty-four samples (five sites) of the anorthosites in the Arden Pluton. One component, with D = 325[deg], I = -75[deg], k = 32, [alpha]95 = 13.6[deg], was isolated in many samples by progressive alternating field demagnetization and in the remainder of the collection by the use of intersecting great circles of remagnetization. The corresponding pole is located at 16[deg]N, 303[deg]E, dp = 22.7[deg], dm = 24.9[deg]. Assuming the age of the last metamorphism (Taconic, ca. 440 Ma) of the Cambrian Arden Pluton to be the age of the magnetization, this pole deviates significantly from coeval poles thus far obtained from the North American craton. The preferred explanation for this deviation is that the Arden Pluton and the surrounding Piedmont rocks belonged to a different Early Paleozoic plate on the south or east side of the Iapetus Ocean, most likely the African (Gondwana) plate, and that it was transferred to the North American plate during a subsequent continental collision.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/23298/1/0000236.pd

Interlayer pair tunneling and gap anisotropy in YBa2_2Cu3_3O7−δ_{7-\delta}

Recent ARPES measurement observed a large $ab$-axis gap anisotropy, $\Delta(0,\pi)/\Delta(\pi,0)=1.5$, in clean YBa$_2$Cu$_3$O$_{7-\delta}$. This indicates that some sub-dominant component may exist in the $d_{x^2-y^2}$-wave dominant gap. We propose that the interlayer pairing tunneling contribution can be determined through the investigation of the order parameter anisotropy. Their potentially observable features in transport and spin dynamics are also studied.Comment: 4 pages, 3 figure

Application of Reflected Global Navigation Satellite System (GNSS-R) Signals in the Estimation of Sea Roughness Effects in Microwave Radiometry

In February-March 2009 NASA JPL conducted an airborne field campaign using the Passive Active L-band System (PALS) and the Ku-band Polarimetric Scatterometer (PolSCAT) collecting measurements of brightness temperature and near surface wind speeds. Flights were conducted over a region of expected high-speed winds in the Atlantic Ocean, for the purposes of algorithm development for salinity retrievals. Wind speeds encountered were in the range of 5 to 25 m/s during the two weeks deployment. The NASA-Langley GPS delay-mapping receiver (DMR) was also flown to collect GPS signals reflected from the ocean surface and generate post-correlation power vs. delay measurements. This data was used to estimate ocean surface roughness and a strong correlation with brightness temperature was found. Initial results suggest that reflected GPS signals, using small low-power instruments, will provide an additional source of data for correcting brightness temperature measurements for the purpose of sea surface salinity retrievals

Evidence for the Presentation of Major Histocompatibility Complex Class I–restricted Epstein-Barr Virus Nuclear Antigen 1 Peptides to CD8+ T Lymphocytes

The Epstein-Barr virus (EBV)-encoded nuclear antigen 1 (EBNA1) is expressed in all EBV-associated tumors, making it an important target for immunotherapy. However, evidence for major histocompatibility complex (MHC) class I–restricted EBNA1 peptides endogenously presented by EBV-transformed B and tumor cells remains elusive. Here we describe for the first time the identification of an endogenously processed human histocompatibility leukocyte antigen (HLA)-B8–restricted EBNA1 peptide that is recognized by CD8+ T cells. T cell recognition could be inhibited by the treatment of target cells with proteasome inhibitors that block the MHC class I antigen processing pathway, but not by an inhibitor (chloroquine) of MHC class II antigen processing. We also demonstrate that new protein synthesis is required for the generation of the HLA-B8 epitope for T cell recognition, suggesting that defective ribosomal products (DRiPs) are the major source of T cell epitopes. Experiments with protease inhibitors indicate that some serine proteases may participate in the degradation of EBNA1 DRiPs before they are further processed by proteasomes. These findings not only provide the first evidence of the presentation of an MHC class I–restricted EBNA1 epitope to CD8+ T cells, but also offer new insight into the molecular mechanisms involved in the processing and presentation of EBNA1

Doping dependence of the resonance peak and incommensuration in high-TcT_{c} superconductors

The doping and frequency evolutions of the incommensurate spin response and the resonance mode are studied based on the scenario of the Fermi surface topology. We use the slave-boson mean-field approach to the $t-t^{\prime}-J$ model and including the antiferromagnetic fluctuation correction in the random-phase approximation. We find that the equality between the incommensurability and the hole concentration is reproduced at low frequencies in the underdoped regime. This equality observed in experiments was explained {\it only} based on the stripe model before. We also obtain the downward dispersion for the spin response and predict its doping dependence for further experimental testing, as well as a proportionality between the low-energy incommensurability and the resonance energy. Our results suggest a common origin for the incommensuration and the resonance peak based on the Fermi surface topology and the d-wave symmetry.Comment: 5 pages, 4 PS figure

Mitochondrial Mutations in Adenoid Cystic Carcinoma of the Salivary Glands

Background: The MitoChip v2.0 resequencing array is an array-based technique allowing for accurate and complete sequencing of the mitochondrial genome. No studies have investigated mitochondrial mutation in salivary gland adenoid cystic carcinomas. Methodology: The entire mitochondrial genome of 22 salivary gland adenoid cystic carcinomas (ACC) of salivary glands and matched leukocyte DNA was sequenced to determine the frequency and distribution of mitochondrial mutations in ACC tumors. Principal Findings: Seventeen of 22 ACCs (77%) carried mitochondrial mutations, ranging in number from 1 to 37 mutations. A disproportionate number of mutations occurred in the D-loop. Twelve of 17 tumors (70.6%) carried mutations resulting in amino acid changes of translated proteins. Nine of 17 tumors (52.9%) with a mutation carried an amino acid changing mutation in the nicotinamide adenine dinucleotide dehydrogenase (NADH) complex. Conclusions/Significance: Mitochondrial mutation is frequent in salivary ACCs. The high incidence of amino acid changing mutations implicates alterations in aerobic respiration in ACC carcinogenesis. D-loop mutations are of unclear significance

Millennial‐scale climatic change during the Last Interglacial Period: Superparamagnetic sediment proxy from Paleosol S1, western Chinese Loess Plateau

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/94646/1/grl12218.pd