Thermal cycling test of a flexible solar cell module

Flexible rolled-up solar array module thermal cycling test

Absolute properties of the main-sequence eclipsing binary FM Leo

First spectroscopic and new photometric observations of the eclipsing binary FM Leo are presented. The main aims were to determine orbital and stellar parameters of two components and their evolutionary stage. First spectroscopic observations of the system were obtained with DDO and PST spectrographs. The results of the orbital solution from radial velocity curves are combined with those derived from the light-curve analysis (ASAS-3 photometry and supplementary observations of eclipses with 1 m and 0.35 m telescopes) to derive orbital and stellar parameters. JKTEBOP, Wilson-Devinney binary modelling codes and a two-dimensional cross-correlation (TODCOR) method were applied for the analysis. We find the masses to be M_1 = 1.318 $\pm$ 0.007 and M_2 = 1.287 $\pm$ 0.007 M_sun, the radii to be R_1 = 1.648 $\pm$ 0.043 and R_2 = 1.511 $\pm$ 0.049 R_sun for primary and secondary stars, respectively. The evolutionary stage of the system is briefly discussed by comparing physical parameters with current stellar evolution models. We find the components are located at the main sequence, with an age of about 3 Gyr.Comment: 5 pages, 4 figures, to appear in MNRA

Evidence That a Lipolytic Enzyme—Hematopoietic-Specific Phospholipase C-β2—Promotes Mobilization of Hematopoietic Stem Cells by Decreasing Their Lipid Raft-Mediated Bone Marrow Retention and Increasing the Promobilizing Effects of Granulocytes

Hematopoietic stem/progenitor cells (HSPCs) reside in the bone marrow (BM) microenvironment and are retained there by the interaction of membrane lipid raft-associated receptors, such as the α-chemokine receptor CXCR4 and the α4β1-integrin (VLA-4, very late antigen 4 receptor) receptor, with their respective specific ligands, stromal-derived factor 1 and vascular cell adhesion molecule 1, expressed in BM stem cell niches. The integrity of the lipid rafts containing these receptors is maintained by the glycolipid glycosylphosphatidylinositol anchor (GPI-A). It has been reported that a cleavage fragment of the fifth component of the activated complement cascade, C5a, has an important role in mobilizing HSPCs into the peripheral blood (PB) by (i) inducing degranulation of BM-residing granulocytes and (ii) promoting their egress from the BM into the PB so that they permeabilize the endothelial barrier for subsequent egress of HSPCs. We report here that hematopoietic cell-specific phospholipase C-β2 (PLC-β2) has a crucial role in pharmacological mobilization of HSPCs. On the one hand, when released during degranulation of granulocytes, it digests GPI-A, thereby disrupting membrane lipid rafts and impairing retention of HSPCs in BM niches. On the other hand, it is an intracellular enzyme required for degranulation of granulocytes and their egress from BM. In support of this dual role, we demonstrate that PLC-β2-knockout mice are poor mobilizers and provide, for the first time, evidence for the involvement of this lipolytic enzyme in the mobilization of HSPCs

CASR (Calcium-Sensing Receptor)

Review on CASR, with data on DNA/RNA, on the protein encoded and where the gene is implicated

The interactive effects of press/pulse intensity and duration on regime shifts at multiple scales

Citation: Ratajczak, Z., D'Odorico, P., Collins, S. L., Bestelmeyer, B. T., Isbell, F. I., & Nippert, J. B. (2017). The interactive effects of press/pulse intensity and duration on regime shifts at multiple scales. Ecological Monographs, 87(2), 198-218. doi:10.1002/ecm.1249Regime shifts are difficult-to-reverse transitions that occur when an ecosystem reorganizes around a new set of self-reinforcing feedbacks. Regime shifts are predicted to occur when the intensity of some exogenous driver variable, such as temperature, annual harvest rate, or nutrient addition rate, gradually approaches and crosses a threshold value, initiating a transition to an alternative state. However, many driver variables now change rapidly as presses or pulses, not gradually, requiring new conceptual frameworks for understanding and predicting regime shifts. We argue that identifying and controlling regime shifts in response to presses and pulses will require a greater focus on the duration, not just the intensity, of changes in driver variables. In ecosystems with slower dynamics, transitions to an alternative state can take years to decades and as a result, a driver press with an intensity capable of resulting in a regime shift over long time spans may fail to cause a regime shift when applied for shorter durations. We illustrate these ideas using simulations of local-scale alternative stable state models and preliminary evidence from long-term grazing and eutrophication experiments. The simulations also suggest that small changes in the duration of driver presses or pulses can determine whether an ecosystem recovers to its original state. These insights may extend to larger scales. In spatially extended simulations that included patchiness, spatial heterogeneity, and spatial connectivity, all patches recovered to their original state after shorter presses. However, once press duration exceeded a threshold, growing proportions of the landscape shifted to an alternative state as press duration increased. We observed similar patchy transitions in a catchment-scale experiment that reinstated frequent fires approximately halfway through a regime shift from grassland to shrubland, initiated by fire suppression. In both the local-and larger-scale models, the threshold duration needed to elicit regime shifts decreased as press intensity increased or when factors counteracting regime shifts weakened. These multiple lines of evidence suggest that conceptualizing regime shifts as an interactive function of the intensity and duration of driver changes will increase understanding of the varying effects of driver presses, pulses, and cycles on ecosystem dynamics

A RECONFIGURABLE ELECTROMAGNETIC BANDGAP STRUCTURE FOR A BEAM STEERING BASE STATION ANTENNA

International audienceThe purpose of this communication is to present the works of a French Industry and Research sponsorized project (RNRT Project) named "BIP" [1]. The goal of this project was to design a beam steering multi-band (GSM/DCS/UMTS) base station antenna. After a presentation of the different partners, we will show how we would solved the problem of the beam steering antenna with a controllable Electromagnetic BandGap (EBG) structure and we will present the results of simulations and experiments in order to validate the concept

Very small embryonic-like stem cells (VSELs) represent a real challenge in stem cell biology : recent pros and cons in the midst of a lively debate

The concept that adult tissue, including bone marrow (BM), contains early-development cells with broader differentiation potential has again been recently challenged. In response, we would like to review the accumulated evidence from several independent laboratories that adult tissues, including BM, harbor a population of very rare stem cells that may cross germ layers in their differentiation potential. Thus, the BM stem cell compartment hierarchy needs to be revisited. These dormant, early-development cells that our group described as very small embryonic-like stem cells (VSELs) most likely overlap with similar populations of stem cells that have been identified in adult tissues by other investigators as the result of various experimental strategies and have been given various names. As reported, murine VSELs have some pluripotent stem cell characteristics. Moreover, they display several epiblast/germline markers that suggest their embryonic origin and developmental deposition in adult BM. Moreover, at the molecular level, changes in expression of parentally imprinted genes (for example, Igf2–H19) and resistance to insulin/insulin-like growth factor signaling (IIS) regulates their quiescent state in adult tissues. In several emergency situations related to organ damage, VSELs can be activated and mobilized into peripheral blood, and in appropriate animal models they contribute to tissue organ/regeneration. Interestingly, their number correlates with lifespan in mice, and they may also be involved in some malignancies. VSELs have been successfully isolated in several laboratories; however, some investigators experience problems with their isolation