Traffic differentiation support in vehicular delay-tolerant networks

Vehicular Delay-Tolerant Networking (VDTN) is a Delay-Tolerant Network (DTN) based architecture concept for transit networks, where vehicles movement and their bundle relaying service is opportunistically exploited to enable non-real time applications, under environments prone to connectivity disruptions, network partitions and potentially long delays. In VDTNs, network resources may be limited, for instance due to physical constraints of the network nodes. In order to be able to prioritize applications traffic according to its requirements in such constrained scenarios, traffic differentiation mechanisms must be introduced at the VDTN architecture. This work considers a priority classes of service (CoS) model and investigates how different buffer management strategies can be combined with drop and scheduling policies, to provide strict priority based services, or to provide custom allocation of network resources. The efficiency and tradeoffs of these proposals is evaluated through extensive simulation.     

Routing and mobility approaches in IPv6 over LoWPAN mesh networks

It is foreseeable that any object in the near future will have an Internet connection—this is the Internet of Things vision. All these objects will be able to exchange and process information, most of them characterized by small size, power constrained, small computing and storage resources. In fact, connecting embedded low‐power devices to the Internet is considered the biggest challenge and opportunity for the Internet. There is a strong trend of convergence towards an Internet‐based solution and the 6LoWPAN may be the convergence solution to achieve the Internet of Things vision. Wireless mesh networks have attracted the interest of the scientific community in recent years. One of the key characteristics of wireless mesh networks is the ability to self‐organize and self‐configure. Mesh networking and mobility support are considered crucial to the Internet of Things success. This paper surveys the available solutions proposed to support routing and mobility over 6LoWPAN mesh networks. Copyright © 2011 John Wiley & Sons, Ltd.     

Long-range effect of cyanide on mercury methylation in a gold mining area in southern Ecuador

Small-scale gold mining in Portovelo-Zaruma, Southern Equador, performed by mercury amalgamation and cyanidation, yields 9-10 t of gold/annum, resulting in annual releases of around 0.65 t of inorganic mercury and 6000 t of sodium cyanide in the local river system. The release of sediments, cyanide, mercury, and other metals present in the ore such as lead, manganese and arsenic significantly reduces biodiversity downstream the processing plants and enriches metals in bottom sediments and biota. However, methylmercury concentrations in sediments downstream the mining area were recently found to be one order of magnitude lower than upstream or in small tributaries. In this study we investigated cyanide, bacterial activity in water and sediment and mercury methylation potentials in sediments along the Puyango river watershed, measured respectively by in-situ spectrophotometry and incubation with ³H-leucine and ²⁰³Hg²⁺.Free cyanide was undetectable (< 1 μg·L^− 1) upstream mining activities, reached 280 μg·L^− 1 a few km downstream the processing plants area and was still detectable about 100 km downstream. At stations with detectable free cyanide in unfiltered water, 50% of it was dissolved and 50% associated to suspended particles. Bacterial activity and mercury methylation in sediment showed a similar spatial pattern, inverse to the one found for free cyanide in water, i.e. with significant values in pristine upstream sampling points (respectively 6.4 to 22 μgC·mg wet weight^− 1·h^− 1 and 1.2 to 19% of total ²⁰³Hg·g dry weight^− 1·day^− 1) and undetectable downstream the processing plants, returning to upstream values only in the most distant downstream stations. The data suggest that free cyanide oxidation was slower than would be expected from the high water turbulence, resulting in a long-range inhibition of bacterial activity and hence mercury methylation. The important mercury fluxes resultant from mining activities raise concerns about its biomethylation in coastal areas where many mangrove areas have been converted to shrimp farming.     

Preparation of antistatic and biodegradable packaging of PLA/PHBV blend-based glassy carbon and graphene nanoplatelets composites

Glassy carbon (GC) and graphene nanoplatelets (GNP) were used as fillers for the preparation of antistatic and biodegradable composites based on poly (lactic acid)/poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PLA/PHBV) blend. In this work, PLA/PHBV (80/20) blends with the addition of different GC contents (0.1, 0.3, and 0.5 wt%) were prepared by melt mixing using a twin-screw extruder, and specimens were injection molded. Furthermore, hybrid composites were prepared with the addition of 5 wt% of GNP and different GC contents (0.1, 0.3, and 0.5 wt%) using the same processing. The effect of the addition of GC and GNP on the mechanical, electrical, and electromagnetic properties and its effect on the biodegradability of the PLA/PHVB blend was evaluated. The simultaneous addition of GC (0.3 and 0.5 wt%) and GNP (5 wt%) significantly increases the elastic modulus and decreases the electrical resistivity, becoming suitable for electrostatic discharge protection packaging applications. The hybrid composite GC0.5/GNP5 reached a maximum value of total attenuation (4.5 dB), which corresponds to 60% EMI shielding. The degree of crystallinity affects biodegradability more than the type or presence of carbon material. After 110 days of anaerobic biodegradation, the hybrid composite exhibited 10% biodegradability due to the high degree of crystallinity that hinders the biodegradability process. The hybrid composites with the addition of GC and GNP are very promising for use in antistatic packaging.     

The dual specificity phosphatases M3/6 and MKP-3 are highly selective for inactivation of distinct mitogen-activated protein kinases

The mitogen-activated protein (MAP) kinase family includes extracellular signal-regulated kinase (ERK), c-Jun NH2-terminal kinase/stress-activated protein kinase (JNK/SAPK) and p38/RK/CSBP (p38) as structurally and functionally distinct enzyme classes. Here we describe two new dual specificity phosphatases of the CL100/MKP-1 family that are selective for inactivating ERK or JNK/SAPK and p38 MAP kinases when expressed in COS-7 cells. M3/6 is the first phosphatase of this family to display highly specific inactivation of JNK/SAPK and p38 MAP kinases. Although stress-induced activation of p54 SAPKbeta, p46 SAPKgamma (JNK1) or p38 MAP kinases is abolished upon co-transfection with increasing amounts of M3/6 plasmid, epidermal growth factor-stimulated ERK1 is remarkably insensitive even to the highest levels of M3/6 expression obtained. In contrast to M3/6, the dual specificity phosphatase MKP-3 is selective for inactivation of ERK family MAP kinases. Low level expression of MKP-3 blocks totally epidermal growth factor-stimulated ERK1, whereas stress-induced activation of p54 SAPKbeta and p38 MAP kinases is inhibited only partially under identical conditions. Selective regulation by M3/6 and MKP-3 was also observed upon chronic MAP kinase activation by constitutive p21(ras) GTPases. Hence, although M3/6 expression effectively blocked p54 SAPKbeta activation by p21(rac) (G12V), ERK1 activated by p21(ras) (G12V) was insensitive to this phosphatase. ERK1 activation by oncogenic p21(ras) was, however, blocked totally by co-expression of MKP-3. This is the first report demonstrating reciprocally selective inhibition of different MAP kinases by two distinct dual specificity phosphatases.     

Diversity Enhancement of Coded Spread Spectrum Video Watermarking

This paper analyses the effect of signal combination techniques in videowatermark detection. A spatial spread spectrum based watermarking techique isused as embedding method, in combination with common error correction codes(BCH, Reed-Solomon with multilevel signaling, binary convolutional codes withViterbi decoding). Besides an analytical evaluation of the bit error rate, theeffectiveness of the channel coding and diversity techniques is also assessedexperimentally under MPEG-2 video compression.     

A novel role for ursodeoxycholic acid in inhibiting apoptosis by modulating mitochondrial membrane perturbation

The hydrophilic bile salt ursodeoxycholic acid (UDCA) protects against the membrane-damaging effects associated with hydrophobic bile acids. This study was undertaken to (a) determine if UDCA inhibits apoptosis from deoxycholic acid (DCA), as well as from ethanol, TGF-beta1, Fas ligand, and okadaic acid; and to (b) determine whether mitochondrial membrane perturbation is modulated by UDCA. DCA induced significant hepatocyte apoptosis in vivo and in isolated hepatocytes determined by terminal transferase-mediated dUTP-digoxigenin nick end-labeling assay and nuclear staining, respectively (P < 0.001). Apoptosis in isolated rat hepatocytes increased 12-fold after incubation with 0.5% ethanol (P < 0.001). HuH-7 cells exhibited increased apoptosis with 1 nM TGF-beta1 (P < 0. 001) or DCA at >/= 100 microM (P < 0.001), as did Hep G2 cells after incubation with anti-Fas antibody (P < 0.001). Finally, incubation with okadaic acid induced significant apoptosis in HuH-7, Saos-2, Cos-7, and HeLa cells. Coadministration of UDCA with each of the apoptosis-inducing agents was associated with a 50-100% inhibition of apoptotic changes (P < 0.001) in all the cell types. Also, UDCA reduced the mitochondrial membrane permeability transition (MPT) in isolated mitochondria associated with both DCA and phenylarsine oxide by > 40 and 50%, respectively (P < 0.001). FACS(R) analysis revealed that the apoptosis-inducing agents decreased the mitochondrial transmembrane potential and increased reactive oxygen species production (P < 0.05). Coadministration of UDCA was associated with significant prevention of mitochondrial membrane alterations in all cell types. The results suggest that UDCA plays a central role in modulating the apoptotic threshold in both hepatocytes and nonliver cells, and inhibition of MPT is at least one pathway by which UDCA protects against apoptosis.     

Hydrophobic polymers for liquid cleaning formulations

A patented method to provide acrylic acid:styrene (AA:Sty) copolymers with a variety of AA:Sty mole ratios is described. This method allows the polymer to be provided as a solution in water with up to 50 mol% styrene. The addition of significant amounts of styrene provides increased polymer solubility in liquid laundry detergents without sacrificing the traditional benefits of typical polycarboxylates. Studies were run in a Tergotometer and full-scale U.S. washing machine, showing particulate soil antiredeposition performance equivalent to poly(acrylic acid) with a molecular weight of 4500 and improved oily soil antiredeposition. The dry polymer is soluble in several glycols, a behavior not typically seen with polycarboxylates.     

Ozonation of unstretched natural rubber film from Hevea brasiliensis studied by ozone consumption and 13C NMR

Unstretched films of natural rubber (NR) from Hevea brasiliensis were exposed to ozone flow of 15 ml min^?1 from 4 to 300 min. The efficiency of reaction was determined by ozone consumption of NR films. Plots of reacted ozone mass versus film thickness show that the ozone penetration and the ozone reaction progressed into deeper layers (170 µm) than described in the literature (～0.5 µm). The previous proposed model based on viscometry measurements was corroborated by ozone consumption results. The effect of thickness on the O₃/NR stoichiometric ratio indicated that the diffusion process that controls the ozonation in unstretched film does not consist of the boundary progression behind which all reactive sites have been saturated. Ozonation in unstretched rubber film, while being less efficient than ozonolysis in solution, does have a reaction efficiency of the same order of magnitude. NMR spectroscopy was used to characterise the products formed by ozonation. Copyright © 2004 Society of Chemical Industry