Control of the Spanwise Distribution of Circulation on NACA 0012 and Flat Plate Wings

Open-loop active flow control is used to modify the spanwise distribution of circulation around an NACA 0012 and flat plate wing. The leading edge on both airfoils and tip regions of the NACA airfoil contain spatially localized actuators that can be independently controlled in terms of amplitude and frequency, allowing the spanwise distribution of circulation to be modified. Different orientations of the pulsed-blowing actuators were used to provide upstream, downstream, in-line with the flow, and outward span components of actuation. The actuation effectiveness was documented using force balance measurements of the lift and drag, smoke-wire visualization, surface pressure measurements and PIV velocity field measurements. Actuation with an upstream component is shown to be far more effective in reducing the separated region than actuation in the streamwise direction. Initial measurements of the change in circulation on the suction surface of the airfoil indicate that spatially localized forcing produces global changes over the wing, primarily associated with the reduction in size of the separated flow region

Bioaccessibility of PBDEs present in indoor dust: a novel dialysis membrane method with a Tenax TA® absorption sink

Human uptake of flame retardants (FRs) such as polybrominated diphenyl ethers (PBDEs) via indoor dust ingestion is commonly considered as 100% bioaccessible, leading to potential risk overestimation. Here, we present a novel in vitro colon-extended physiologically-based extraction test (CE-PBET) with Tenax TA® as an absorptive "sink" capable to enhance PBDE gut bioaccessibility. A cellulose-based dialysis membrane (MW cut-off 3.5kDa) with high pH and temperature tolerance was used to encapsulate Tenax TA®, facilitating efficient physical separation between the absorbent and the dust, while minimizing re-absorption of the ingested PBDEs to the dust particles. As a proof of concept, PBDE-spiked indoor dust samples (n=3) were tested under four different conditions; without any Tenax TA® addition (control) and with three different Tenax TA® loadings (i.e. 0.25, 0.5 or 0.75g). Our results show that in order to maintain a constant sorptive gradient for the low MW PBDEs, 0.5g of Tenax TA® are required in CE-PBET. Tenax TA® inclusion (0.5g) resulted in 40% gut bioaccessibility for BDE153 and BDE183, whereas greater bioaccessibility values were seen for less hydrophobic PBDEs such as BDE28 and BDE47 (~60%). When tested using SRM 2585 (n=3), our new Tenax TA® method did not present any statistically significant effect (p>0.05) between non-spiked and PBDE-spiked SRM 2585 treatments. Our study describes an efficient method where due to the sophisticated design, Tenax TA® recovery and subsequent bioaccessibility determination can be simply and reliably achieved

Surface Distributions for Eddy Current Probes

This paper is concerned with the computation of the thin-skin solution for eddy current distributions induced in the presence of surface breaking flaws. Earlier work [1], [2], [3], [4] dealt with cases where the distribution induced in the absence of a flaw was uniform. An unfolding technique was developed which reduced the determination of the surface field to a classical two-dimensional potential problem. Exact solutions were obtained by complex potential methods for circular-arc cracks in [1], [2] and for rectangular and triangular cracks in [3], but the main focus of attention in this last work was on semi-elliptical cracks since it is found in practice that many surface fatigue cracks grow with a plan form which can be closely approximated by a half ellipse. This case was not amenable to exact treatment, but the introduction of elliptic co-ordinates allowed a Fourier series solution to be calculated

Death receptor 3 (TNFRSF25) increases mineral apposition by osteoblasts and region specific new bone formation in the axial skeleton of male DBA/1 mice

Fraser L. Collins and this work were funded by an Arthritis Research UK PhD studentship (Grant Code: 18598) awarded to Anwen S. Williams, Eddie C. Y. Wang, and Michael D. Stone. Eddie C. Y. Wang was additionally funded by MRC Project Grant G0901119. Funding for open access was kindly provided by Cardiff University.Peer reviewedPublisher PD

Accuracy of core mass estimates in simulated observations of dust emission

We study the reliability of mass estimates obtained for molecular cloud cores using sub-millimetre and infrared dust emission. We use magnetohydrodynamic simulations and radiative transfer to produce synthetic observations with spatial resolution and noise levels typical of Herschel surveys. We estimate dust colour temperatures using different pairs of intensities, calculate column densities and compare the estimated masses with the true values. We compare these results to the case when all five Herschel wavelengths are available. We investigate the effects of spatial variations of dust properties and the influence of embedded heating sources. Wrong assumptions of dust opacity and its spectral index beta can cause significant systematic errors in mass estimates. These are mainly multiplicative and leave the slope of the mass spectrum intact, unless cores with very high optical depth are included. Temperature variations bias colour temperature estimates and, in quiescent cores with optical depths higher than for normal stable cores, masses can be underestimated by up to one order of magnitude. When heated by internal radiation sources the observations recover the true mass spectra. The shape, although not the position, of the mass spectrum is reliable against observational errors and biases introduced in the analysis. This changes only if the cores have optical depths much higher than expected for basic hydrostatic equilibrium conditions. Observations underestimate the value of beta whenever there are temperature variations along the line of sight. A bias can also be observed when the true beta varies with wavelength. Internal heating sources produce an inverse correlation between colour temperature and beta that may be difficult to separate from any intrinsic beta(T) relation of the dust grains. This suggests caution when interpreting the observed mass spectra and the spectral indices.Comment: Revised version, 17 pages, 17 figures, submitted to A&

Mechanisms of Acute Eosinophil Mobilization from the Bone Marrow Stimulated by Interleukin 5: The Role of Specific Adhesion Molecules and Phosphatidylinositol 3-Kinase

Mobilization of bone marrow eosinophils is a critical early step in their trafficking to the lung during allergic inflammatory reactions. We have shown previously that the cytokine interleukin (IL)-5, generated during an allergic inflammatory reaction in the guinea pig, acts systemically to mobilize eosinophils from the bone marrow. Here, we have investigated the mechanisms underlying this release process. Examination by light and electron microscopy revealed the rapid migration of eosinophils from the hematopoietic compartment and across the bone marrow sinus endothelium in response to IL-5. Using an in situ perfusion system of the guinea pig hind limb, we showed that IL-5 stimulated a dose-dependent selective release of eosinophils from the bone marrow. Eosinophils released from the bone marrow in response to IL-5 expressed increased levels of β2 integrin and a decrease in L-selectin, but no change in α4 integrin levels. A β2 integrin–blocking antibody markedly inhibited the mobilization of eosinophils from the bone marrow stimulated by IL-5. In contrast, an α4 integrin blocking antibody increased the rate of eosinophil mobilization induced by IL-5. In vitro we demonstrated that IL-5 stimulates the selective chemokinesis of bone marrow eosinophils, a process markedly inhibited by two structurally distinct inhibitors of phosphatidylinositol 3-kinase, wortmannin and LY294002. Wortmannin was also shown to block eosinophil release induced by IL-5 in the perfused bone marrow system. The parallel observations on the bone marrow eosinophil release process and responses in isolated eosinophils in vitro suggest that eosinophil chemokinesis is the driving force for release in vivo and that this release process is regulated by α4 and β2 integrins acting in opposite directions

CCL3 and MMP-9 are induced by TL1A during death receptor 3 (TNFRSF25)-dependent osteoclast function and systemic bone loss

FLC was funded by an Arthritis Research UK PhD studentship (Grant code: 18598) awarded to ASW, ECYW and MDS. JOW was funded by a British Heart Foundation PhD studentship (Reference: FS/11/26/ 28750). ACB's PhD studentship was jointly funded by the School of Medicine and Rheumatology Research Fund (Cardiff University) and LJ's PhD studentship was jointly funded by the School of Medicine and the President's Scholarship Fund (Cardiff University) awarded to ASW. ECYW was additionally funded by MRC Project Grant G0901119.Peer reviewedPublisher PD

Control of Flow Structure on a Semi-Circular Planform Wing

Active flow control is used to modify the lift, drag and pitching moments on a semicircular wing with aspect ratio, AR = 2, and chord Reynolds number is 68,000. The wing is mounted on a pitch/plunge sting mechanism that responds to the instantaneous loads and moments acting on the wing. The leading edge of the airfoil contains 16 spatially localized actuators that can be independently controlled. Smoke wire visualization, surface pressure and six-component force balance measurements are used to characterize the effects of openloop forcing. The lift coefficients on the steady wing are enhanced with the actuation, similar to the effect of dynamic stall vortex lift enhancement that occurs during a pitch up maneuver. Surface pressure measurements are being used to construct a flow model for use in feedback control. Progress toward the goal of designing a feedback controller to stabilize the flight of the model in an oscillatory freestream is discussed