Rate Control State-of-the-art Survey

The majority of Internet traffic use Transmission Control Protocol (TCP) as the transport level protocol. It provides a reliable ordered byte stream for the applications. However, applications such as live video streaming place an emphasis on timeliness over reliability. Also a smooth sending rate can be desirable over sharp changes in the sending rate. For these applications TCP is not necessarily suitable. Rate control attempts to address the demands of these applications. An important design feature in all rate control mechanisms is TCP friendliness. We should not negatively impact TCP performance since it is still the dominant protocol. Rate Control mechanisms are classified into two different mechanisms: window-based mechanisms and rate-based mechanisms. Window-based mechanisms increase their sending rate after a successful transfer of a window of packets similar to TCP. They typically decrease their sending rate sharply after a packet loss. Rate-based solutions control their sending rate in some other way. A large subset of rate-based solutions are called equation-based solutions. Equation-based solutions have a control equation which provides an allowed sending rate. Typically these rate-based solutions react slower to both packet losses and increases in available bandwidth making their sending rate smoother than that of window-based solutions. This report contains a survey of rate control mechanisms and a discussion of their relative strengths and weaknesses. A section is dedicated to a discussion on the enhancements in wireless environments. Another topic in the report is bandwidth estimation. Bandwidth estimation is divided into capacity estimation and available bandwidth estimation. We describe techniques that enable the calculation of a fair sending rate that can be used to create novel rate control mechanisms.Peer reviewe

Air Filtration in HVAC Systems

The Guidebook presents the theory of air filtration with some basic principles of the physics of pollutants and their effects on indoor quality. The main focus is on practical design, installation and operation of filters in air handling systems. It is intended for the use of designers, manufacturers, installers, and building owners. With its theory, practical solutions and illustrations it is also an excellent textbook for the vocational training of various experts in building services engineering

Temporal and Spatial Variation in Scots Pine Resin Pressure and Composition

Resin is a first-line defense in pine trees, but important questions regarding its temporal and spatial variation remain unsolved. Resin pressure varies according to water potential in dry conditions, but in moist conditions, it follows temperature dynamics for a yet unknown reason. Relations between resin composition, resin pressure, and shoot monoterpene emissions are also unquantified. To gain mechanistic understanding on the resin dynamics in a boreal forest, we measured temperature and water potential dependency of Scots pine resin pressure. We attempted to quantify the temperature dependency of resin pressure in terms of three contributions: 1) saturation vapor pressure, 2) thermal expansion, and 3) N2, O2, and CO2 solubility. We also analyzed monoterpene composition in the resin and the shoot emissions of 16 pines with gas chromatography mass spectrometry to study their interrelations. We show that in moist conditions, resin pressure is driven by temperature at a diurnal scale, but also affected by soil water potential at a day-to-day scale. Diurnal temperature dependency was explained by thermal expansion of resin and changes in bubble volume due to changes in gas solubility in resin with temperature. Resin pressures correlated also with total monoterpene and α-pinene content in resin and with total monoterpene and ∆3-carene and terpinolene emissions from shoots.Resin is a first-line defense in pine trees, but important questions regarding its temporal and spatial variation remain unsolved. Resin pressure varies according to water potential in dry conditions, but in moist conditions, it follows temperature dynamics for a yet unknown reason. Relations between resin composition, resin pressure, and shoot monoterpene emissions are also unquantified. To gain mechanistic understanding on the resin dynamics in a boreal forest, we measured temperature and water potential dependency of Scots pine resin pressure. We attempted to quantify the temperature dependency of resin pressure in terms of three contributions: (1) saturation vapor pressure, (2) thermal expansion, and (3) N2, O2, and CO2 solubility. We also analyzed monoterpene composition in the resin and the shoot emissions of 16 pines with gas chromatography mass spectrometry to study their interrelations. We show that in moist conditions, resin pressure is driven by temperature at a diurnal scale, but also affected by soil water potential at a day-to-day scale. Diurnal temperature dependency was explained by thermal expansion of resin and changes in bubble volume due to changes in gas solubility in resin with temperature. Resin pressures correlated also with total monoterpene and α-pinene content in resin and with total monoterpene and Δ3-carene and terpinolene emissions from shoots.Peer reviewe

Only IL-1β release is inflammasome-dependent upon ultraviolet B irradiation although IL-18 is also secreted

Abstract DNA damage accumulates in aged postmitotic retinal pigment epithelium (RPE) cells, a phenomenon associated with the development of age-related macular degeneration. In this study, we have experimentally induced DNA damage by ultraviolet B (UVB) irradiation in interleukin-1α (IL-1α)-primed ARPE-19 cells and examined inflammasome-mediated signaling. To reveal the mechanisms of inflammasome activation, cells were additionally exposed to high levels of extracellular potassium chloride, n-acetyl-cysteine, or mitochondria-targeted antioxidant MitoTEMPO, prior to UVB irradiation. Levels of interleukin-18 (IL-18) and IL-1? mRNAs were detected with qRT-PCR and secreted amounts of IL-1?, IL-18, and caspase-1 were measured with ELISA. The role of nucleotide-binding domain and leucine-rich repeat pyrin containing protein 3 (NLRP3) in UVB-induced inflammasome activation was verified by using the NLRP3-specific siRNA. Reactive oxygen species (ROS) levels were measured immediately after UVB exposure using the cell-permeant 2?,7?-dichlorodihydrofluorescein diacetate (H2DCFDA) indicator, the levels of cyclobutane pyrimidine dimers were assayed by cell-based ELISA, and the extracellular levels of adenosine triphosphate (ATP) determined using a commercial bioluminescence assay. We found that pro-IL-18 was constitutively expressed by ARPE-19 cells, whereas the expression of pro-IL-1? was inducible by IL-1α priming. UVB induced the release of mature IL-18 and IL-1? but NLRP3 contributed only to the secretion of IL-1?. At the mechanistic level, the release of IL-1? was regulated by K+ efflux, whereas the secretion of IL-18 was dependent on ROS production. As well as K+ efflux, the cells released ATP following UVB exposure. Collectively, our data suggest that UVB clearly stimulates the secretion of mature IL-18 as a result of ROS induction, and this response is associated with DNA damage. Moreover, in human RPE cells, K+ efflux mediates the UVB-activated NLRP3 inflammasome signaling, leading to the processing of IL-1?.Peer reviewe

Influence of Hsp90 and HDAC Inhibition and Tubulin Acetylation on Perinuclear Protein Aggregation in Human Retinal Pigment Epithelial Cells

Retinal pigment epithelial (RPE) cells are continually exposed to oxidative stress that contributes to protein misfolding, aggregation and functional abnormalities during aging. The protein aggregates formed at the cell periphery are delivered along the microtubulus network by dynein-dependent retrograde trafficking to a juxtanuclear location. We demonstrate that Hsp90 inhibition by geldanamycin can effectively suppress proteasome inhibitor, MG-132-induced protein aggregation in a way that is independent of HDAC inhibition or the tubulin acetylation levels in ARPE-19 cells. However, the tubulin acetylation and polymerization state affects the localization of the proteasome-inhibitor-induced aggregation. These findings open new perspectives for understanding the pathogenesis of protein aggregation in retinal cells and can be useful for the development of therapeutic treatments to prevent retinal cell deterioration

Continuous Team Semantics

Peer reviewe

Continuous Team Semantics

We study logics with team semantics in computable metric spaces. We show how to define approximate versions of the usual independence/dependence atoms. For restricted classes of formulae, we show that we can assume w.l.o.g.~that teams are closed sets. This then allows us to import techniques from computable analysis to study the complexity of formula satisfaction and model checking

Burst analysis tool for developing neuronal networks exhibiting highly varying action potential dynamics

In this paper we propose a firing statistics based neuronal network burst detection algorithm for neuronal networks exhibiting highly variable action potential dynamics. Electrical activity of neuronal networks is generally analyzed by the occurrences of spikes and bursts both in time and space. Commonly accepted analysis tools employ burst detection algorithms based on predefined criteria. However, maturing neuronal networks, such as those originating from human embryonic stem cells (hESCs), exhibit highly variable network structure and time-varying dynamics. To explore the developing burst/spike activities of such networks, we propose a burst detection algorithm which utilizes the firing statistics based on interspike interval (ISI) histograms. Moreover, the algorithm calculates ISI thresholds for burst spikes as well as for pre-burst spikes and burst tails by evaluating the cumulative moving average (CMA) and skewness of the ISI histogram. Because of the adaptive nature of the proposed algorithm, its analysis power is not limited by the type of neuronal cell network at hand. We demonstrate the functionality of our algorithm with two different types of microelectrode array (MEA) data recorded from spontaneously active hESC-derived neuronal cell networks. The same data was also analyzed by two commonly employed burst detection algorithms and the differences in burst detection results are illustrated. The results demonstrate that our method is both adaptive to the firing statistics of the network and yields successful burst detection from the data. In conclusion, the proposed method is a potential tool for analyzing of hESC-derived neuronal cell networks and thus can be utilized in studies aiming to understand the development and functioning of human neuronal networks and as an analysis tool for in vitro drug screening and neurotoxicity assays

UV-B-Induced Inflammasome Activation Can Be Prevented by Cis-Urocanic Acid in Human Corneal Epithelial Cells

PURPOSE. The cornea is continually exposed to highly energetic solar UV-B (280-320 nm). Our aim was to investigate whether UV-B triggers the activation of NLRP3 inflammasomes and the production of IL-1 beta and/or IL-18 in human corneal epithelial (HCE) cells. Additionally, we studied the capability of cis-urocanic acid (cis-UCA) to prevent inflammasome activation or alleviate inflammation through other signaling pathways. METHODS. HCE-2 cell line and primary HCE cells were primed using lipopolysaccharide or TNF-alpha. Thereafter, cells were exposed to UV-B before or after the addition of cis-UCA or caspase-1 inhibitor. Caspase-1 activity was measured from cell lysates by an enzymatic assay. IL-1 beta, IL-18, IL-6, IL-8, and NLRP3 levels were detected using the ELISA method from cell culture media. Additionally, intracellular NLRP3 levels were determined by the Western blot technique, and cytotoxicity was measured by the LDH assay. RESULTS. UV-B exposure significantly increased caspase-1 activity in TNF-alpha-primed HCE cells. This result was consistent with the concurrently induced IL-1 beta secretion. Both caspase-1 activity and release of IL-1 beta were reduced by cis-UCA. Additionally, UV-B stimulated the caspase-1-independent production of IL-18, an effect also reduced by cis-UCA. Cis-UCA decreased the release of IL-6, IL-8, and LDH in a time-dependent manner when administered to HCE-2 cells after UV-B exposure. CONCLUSIONS. Our findings demonstrate that UV-B activates inflammasomes in HCE cells. Cis-UCA can prevent the secretion of IL-1 beta and IL-18 and therapeutically reduces the levels of IL-6, IL-8, and LDH in UV-B-stressed HCE cells.Peer reviewe