Precision measurements of the scintillation pulse shape for low-energy recoils in liquid xenon

We present measurements of the scintillation pulse shape in liquid xenon for nuclear recoils (NR) and electronic recoils (ER) at electric fields of 0 to 0.5 kV/cm for energies $<$ 15 keV and $<$ 70 keV electron-equivalent, respectively. The average pulse shapes are well-described by an effective model with two exponential decay components, where both decay times are fit parameters. We find significant broadening of the pulse for ER due to delayed luminescence from the recombination process. In addition to the effective model, we fit a model describing the recombination luminescence for ER at zero field and obtain good agreement. We estimate the best performance of a combined S2/S1 and pulse shape ER/NR discrimination and show that even with 2 ns time resolution, the improvement over S2/S1 discrimination alone is marginal, so that pulse shape discrimination will likely not be useful for future dual-phase liquid xenon experiments looking for elastic dark matter recoil interactions

Folate-targeted immunotherapy effectively treats established adjuvant and collagen-induced arthritis

Activated macrophages express a cell surface receptor for the vitamin folic acid. Because this receptor is inaccessible or not measurably expressed on other normal cells, folic acid has been recently exploited to selectively deliver attached radio-emitters to sites of activated macrophage accumulation, allowing scintigraphic imaging of inflamed joints and organs of arthritic rats. We demonstrate here that folate-linked haptens can also be targeted to activated macrophages, decorating their cell surfaces with highly immunogenic molecules. Under conditions in which the rodent has already been immunized against keyhole limpet hemocyanine-(fluorescein isothiocyanate) FITC, activated macrophages are eliminated. Administration of folate-FITC conjugates to rodents with experimental arthritis attenuates (a) systemic and peri-articular inflammation, (b) bone and cartilage degradation, and (c) arthritis-related body weight loss. Treatment with folate-hapten conjugates is comparable to methotrexate, etanercept, anakinra, and celecoxib at alleviating the symptoms of arthritis. We conclude that reduction of activated macrophages by folate-targeted immunotherapy can ameliorate the symptoms of arthritis in two rodent models of the disease

Ergonomic Analysis of Veterinary Surgical Tasks

Studies have observed injuries and musculoskeletal discomforts among surgeons in human medicine. It is likely that veterinary surgeons endure similar discomfort; however, limited work has been done in this domain. Therefore, this research aims to identify occupational risk factors affecting the upper extremities of leading and assisting surgeons in orthopedic and soft tissue small animal surgeries. As a result, we aim to reduce surgeon injuries by assessing the surgical environment in veterinary care. To collect objective metrics, inertial measurement units (IMUs), heart rate monitors, and Electromyography (EMG) sensors are used. In addition, surveys are used to evaluate perceived pain before and after surgery and the workload of the task. In total, 5 participants were studied over 26 surgeries. Postoperatively, neck discomfort was most commonly recorded. Neck discomfort was reported in two-thirds of the cases by of the orthopedic surgeons and over one-third of the soft tissue surgeries. Average perceived workload was reported higher in orthopedic surgeries compared to soft tissue surgeries. When measuring the deltoid and trapezius muscle activities, orthopedic surgeons exerted about 21% of their maximum muscle force across the two muscle groups and soft tissue surgeons exerted 12%. These results provide insight to surgeons\u27 perceived workload and physical efforts associated with performing surgery, and further applications of this work may translate to modifications to surgical environments or additional surgeon education to reduce physical strains

Percolation Systems away from the Critical Point

This article reviews some effects of disorder in percolation systems even away from the critical density p_c. For densities below p_c, the statistics of large clusters defines the animals problem. Its relation to the directed animals problem and the Lee-Yang edge singularity problem is described. Rare compact clusters give rise to Griffiths singuraties in the free energy of diluted ferromagnets, and lead to a very slow relaxation of magnetization. In biassed diffusion on percolation clusters, trapping in dead-end branches leads to asymptotic drift velocity becoming zero for strong bias, and very slow relaxation of velocity near the critical bias field.Comment: Minor typos fixed. Submitted to Praman

Small heat shock proteins are induced during multiple sclerosis lesion development in white but not grey matter

INTRODUCTION: The important protective role of small heat-shock proteins (HSPs) in regulating cellular survival and migration, counteracting protein aggregation, preventing apoptosis, and regulating inflammation in the central nervous system is now well-recognized. Yet, their role in the neuroinflammatory disorder multiple sclerosis (MS) is largely undocumented. With the exception of alpha B-crystallin (HSPB5), little is known about the roles of small HSPs in disease. RESULTS: Here, we examined the expression of four small HSPs during lesion development in MS, focussing on their cellular distribution, and regional differences between white matter (WM) and grey matter (GM). It is well known that MS lesions in these areas differ markedly in their pathology, with substantially more intense blood-brain barrier damage, leukocyte infiltration and microglial activation typifying WM but not GM lesions. We analysed transcript levels and protein distribution profiles for HSPB1, HSPB6, HSPB8 and HSPB11 in MS lesions at different stages, comparing them with normal-appearing brain tissue from MS patients and non-neurological controls. During active stages of demyelination in WM, and especially the centre of chronic active MS lesions, we found significantly increased expression of HSPB1, HSPB6 and HSPB8, but not HSPB11. When induced, small HSPs were exclusively found in astrocytes but not in oligodendrocytes, microglia or neurons. Surprisingly, while the numbers of astrocytes displaying high expression of small HSPs were markedly increased in actively demyelinating lesions in WM, no such induction was observed in GM lesions. This difference was particularly obvious in leukocortical lesions covering both WM and GM areas. CONCLUSIONS: Since induction of small HSPs in astrocytes is apparently a secondary response to damage, their differential expression between WM and GM likely reflects differences in mediators that accompany demyelination in either WM or GM during MS. Our findings also suggest that during MS, cortical structures fail to benefit from the protective actions of small HSPs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40478-015-0267-2) contains supplementary material, which is available to authorized users