4,917 research outputs found
Some consequences of intense electromagnetic wave injection into space plasmas
The future possibility of actively testing the current understanding of how energetic particles may be accelerated in space or dumped from the radiation belts using intense electromagnetic energy from ground based antennas is discussed. The ground source of radiation is merely a convenience. A space station source for radiation that does not have to pass through the atmosphere and lower ionosphere, is an attractive alternative. The text is divided into two main sections addressing the possibilities of: (1) accelerating electrons to fill selected flux tubes above the Kennel-Petscheck limit for stably trapped fluxes, and (2) using an Alfven maser to cause rapid depletion of energetic protons or electrons from the radiation belts
Production and characterisation of monoclonal antibodies specific for chicken interleukin-2
Using genetic immunisation of mice, we produced antibodies against chicken interleukin-2 (ChIL-2), the first produced against a non-mammalian interleukin. After a final injection with a recombinant ChIL-2 protein, two stable hybridoma cell lines were established which secreted monoclonal antibodies (MAbs) against this cytokine. Specific binding of the two MAbs to recombinant ChIL-2 produced by Escherichia coli and COS-7 cells was demonstrated in an indirect ELISA, Western blotting and dot blots. Both of them were able to neutralise the biological activity of the ChIL-2, but neither allowed the detection of ChIL-2 by flow cytometry
A simulation model of time-dependent plasma-spacecraft interactions
A plasma simulation code is presented that models the time-dependent plasma properties in the vicinity of a spherical, charged spacecraft. After showing agreement with analytic, steady-state theories and ATS-6 satellite data, the following three problems are treated: (1) transient pulses from photoemission at various emission temperatures and ambient plasma conditions, (2) spacecharge limited emission, and (3) simulated plasma oscillations in the long wavelength limit
Terminal Moraine Remnants of the Trail Creek Glacier Northeast of Sun Valley, Idaho
This optional excursion is 8 miles on paved road from the center of Ketchum (Main Street and Sun Valley Road traffic light), northeast through Sun Valley along the Trail Creek Road (fig. 1). A short walk of 10 minutes takes you to the crests of two moraines of very different ages. Here we view and discuss calcareous soils developed into the deposits, the pretty weathering-rinds developed on the sandstone cobbles, and ages of Pinedale and Bull Lake advances. During the Quaternary, an extensive system of mountain glaciers accumulated in the Pioneer and Boulder Mountains and flowed down valleys emanating from the ranges (Evenson and others, 1982, Pearce and others, 1988). An ice field several miles across accumulated in the Trail Creek Summit area and contributed ice to both the northeast-flowing Summit Creek glacier and to south-flowing Trail Creek glacier (fig. 2). Despite barroom talk in Sun Valley and Ketchum, we find no evidence that the resort towns or the Mt. Baldy ski hill were glaciated during the last ice ages. Rather, the glacier of closest approach was the Trail Creek glacier that advanced down valley to about elevation 1,950 m (6,400 ft), where Wilson Creek flows into Trail Creek, about 10 km (6 mi) northeast of the Sun Valley Inn. The remnants of the two terminal moraines are best seen on the spur at the confluence of Wilson Creek and Trail Creek (fig. 3). From the road, facing northeast, the moraines appear as low ridges sloping 12º from the walls of Trail Creek Canyon down to Wilson Creek Canyon. Crest of the upper moraine stands 55 m higher than the lower moraine. The 12º crestal slope down into Wilson Creek, and low position in the valley indicate that this was the terminus of the two glacial advances. Furthermore, only outwash sand and gravel terraces occur below this area; no till or erratics are observed on the canyon walls down valley
Searching for "monogenic diabetes" in dogs using a candidate gene approach
BACKGROUND: Canine diabetes is a common endocrine disorder with an estimated breed-related prevalence ranging from 0.005% to 1.5% in pet dogs. Increased prevalence in some breeds suggests that diabetes in dogs is influenced by genetic factors and similarities between canine and human diabetes phenotypes suggest that the same genes might be associated with disease susceptibility in both species. Between 1-5% of human diabetes cases result from mutations in a single gene, including maturity onset diabetes of the adult (MODY) and neonatal diabetes mellitus (NDM). It is not clear whether monogenic forms of diabetes exist within some dog breeds. Identification of forms of canine monogenic diabetes could help to resolve the heterogeneity of the condition and lead to development of breed-specific genetic tests for diabetes susceptibility. RESULTS: Seventeen dog breeds were screened for single nucleotide polymorphisms (SNPs) in eighteen genes that have been associated with human MODY/NDM. Six SNP associations were found from five genes, with one gene (ZFP57) being associated in two different breeds. CONCLUSIONS: Some of the genes that have been associated with susceptibility to MODY and NDM in humans appear to also be associated with canine diabetes, although the limited number of associations identified in this study indicates canine diabetes is a heterogeneous condition and is most likely to be a polygenic trait in most dog breeds. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2052-6687-1-8) contains supplementary material, which is available to authorized users
Tremor in motor neuron disease may be central rather than peripheral in origin
BACKGROUND AND PURPOSE:
Motor neuron disease (MND) refers to a spectrum of degenerative diseases affecting motor neurons. Recent clinical and post-mortem observations have revealed considerable variability in the phenotype. Rhythmic involuntary oscillations of the hands during action, resembling tremor, can occur in MND, but their pathophysiology has not yet been investigated.
METHODS:
A total of 120 consecutive patients with MND were screened for tremor. Twelve patients with action tremor and no other movement disorders were found. Ten took part in the study. Tremor was recorded bilaterally using surface electromyography (EMG) and triaxial accelerometer, with and without a variable weight load. Power spectra of rectified EMG and accelerometric signal were calculated. To investigate a possible cerebellar involvement, eyeblink classic conditioning was performed in five patients.
RESULTS:
Action tremor was present in about 10% of our population. All patients showed distal postural tremor of low amplitude and constant frequency, bilateral with a small degree of asymmetry. Two also showed simple kinetic tremor. A peak at the EMG and accelerometric recordings ranging from 4 to 12 Hz was found in all patients. Loading did not change peak frequency in either the electromyographic or accelerometric power spectra. Compared with healthy volunteers, patients had a smaller number of conditioned responses during eyeblink classic conditioning.
CONCLUSIONS:
Our data suggest that patients with MND can present with action tremor of a central origin, possibly due to a cerebellar dysfunction. This evidence supports the novel idea of MND as a multisystem neurodegenerative disease and that action tremor can be part of this condition
Effect of donepezil on transcranial magnetic stimulation parameters in Alzheimer's disease
INTRODUCTION: There is a need for a reliable, noninvasive biomarker for Alzheimer's disease (AD). We assessed whether short-latency afferent inhibition (SAI), a transcranial magnetic stimulation paradigm that assesses cholinergic circuits of the brain, could become such a biomarker. METHODS: Nineteen patients with AD underwent four SAI testing sessions. The timing of their usual donepezil dose was altered to create different cholinergic states for each session. This was compared to the SAI results from 20 healthy subjects. RESULTS: SAI was not able to distinguish the different cholinergic states assessed in our study. There appeared to be a diurnal variation in cholinergic function in the control group, which was not present in the AD cohort. DISCUSSION: SAI does not appear to have a role in diagnosis and assessment of AD patients. The loss of diurnal variation, however, warrants further investigation as it may provide further biochemical insights about AD
GSH23.0-0.7+117, a neutral hydrogen shell in the inner Galaxy
GSH23.0-0.7+117 is a well-defined neutral hydrogen shell discovered in the
VLA Galactic Plane Survey (VGPS). Only the blueshifted side of the shell was
detected. The expansion velocity and systemic velocity were determined through
the systematic behavior of the HI emission with velocity. The center of the
shell is at (l,b,v)=(23.05,-0.77,+117 km/s). The angular radius of the shell is
6.8', or 15 pc at a distance of 7.8 kpc. The HI mass divided by the volume of
the half-shell implies an average density n_H = 11 +/- 4 cm^{-3} for the medium
in which the shell expanded. The estimated age of GSH23.0-0.7+117 is 1 Myr,
with an upper limit of 2 Myr. The modest expansion energy of 2 * 10^{48} erg
can be provided by the stellar wind of a single O4 to O8 star over the age of
the shell. The 3 sigma upper limit to the 1.4 GHz continuum flux density
(S_{1.4} < 248 mJy) is used to derive an upper limit to the Lyman continuum
luminosity generated inside the shell. This upper limit implies a maximum of
one O9 star (O8 to O9.5 taking into account the error in the distance) inside
the HI shell, unless most of the incident ionizing flux leaks through the HI
shell. To allow this, the shell should be fragmented on scales smaller than the
beam (2.3 pc). If the stellar wind bubble is not adiabatic, or the bubble has
burst (as suggested by the HI channel maps), agreement between the energy and
ionization requirements is even less likely. The limit set by the non-detection
in the continuum provides a significant challenge for the interpretation of
GSH23.0-0.7+117 as a stellar wind bubble. A similar analysis may be applicable
to other Galactic HI shells that have not been detected in the continuum.Comment: 18 pages, 6 figures. Figures 1 and 4 separately in GIF format.
Accepted for publication in Astrophysical Journa
Continuous Theta Burst Stimulation Over the Dorsolateral Prefrontal Cortex and the Pre-SMA Alter Drift Rate and Response Thresholds Respectively During Perceptual Decision-Making
BACKGROUND: The speed-accuracy trade-off (SAT) refers to the balancing of speed versus accuracy during decision-making. SAT is very commonly investigated with perceptual decision-making tasks such as the moving dots task (MDT). The dorsolateral prefrontal cortex (DLPFC) and the pre-supplementary motor area (pre-SMA) are two brain regions considered to be involved in the control of SAT. OBJECTIVES/HYPOTHESES: The study tested whether the DLPFC and the pre-SMA play an essential role in the control of SAT. We hypothesized that continuous theta burst stimulation (cTBS) over the right DLPFC would primarily alter the rate of accumulation of evidence, whereas stimulation of the pre-SMA would influence the threshold for reaching a decision. METHODS: Fifteen (5 females; mean age = 30, SD =5.40) healthy volunteers participated in the study. We used two versions of the MDT and cTBS over the right DLPFC, pre-SMA and sham stimulation. The drift diffusion model was fit to the behavioural data (reaction time and error rate) in order to calculate the drift rate, boundary separation (threshold) and non-decision time. RESULTS: cTBS over the right DLPFC decreased the rate of accumulation of evidence (i.e. the drift rate from the diffusion model) in high (0.35 and 0.5) but not in low coherence trials. cTBS over the pre-SMA changed the boundary separation/threshold required to reach a decision on accuracy, but not on speed trials. CONCLUSIONS: The results suggest for the first time that both the DLPFC and the pre-SMA make essential but distinct contributions to the modulation of SAT
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