Modelling gross primary production of a tropical semi-deciduous forest in the southern Amazon Basin

Semi-deciduous forest in the Amazon Basin is sensitive to temporal variation in surface water availability that can limit seasonal rates of leaf and canopy gas exchange. We estimated the seasonal dynamics of gross primary production (GPP) over 3 years (2005–2008) using eddy covariance and assessed canopy spectral reflectance using MODIS imagery for a mature tropical semi-deciduous forest located near Sinop, Mato Grosso, Brazil. A light-use efficiency model, known as the Vegetation Photosynthesis Model (VPM), was used to estimate seasonal and inter-annual variations in GPP as a function of the enhanced vegetation index (EVI), the land surface water index (LSWI), and local meteorology. Our results indicate that the standard VPM was incapable of reproducing the seasonal variation in GPP, primarily because the model overestimated dry-season GPP. In the standard model, the scalar function that alters light-use efficiency (ε_g) as a function of water availability (W_scalar) is calculated as a linear function of the LSWI derived from MODIS; however, the LSWI is negatively correlated with several measures of water availability including precipitation, soil water content, and relative humidity (RH). Thus, during the dry season, when rainfall, soil water content, and RH are low, LSWI, and therefore, W_scalar, are at a seasonal maximum. Using previous research, we derived new functions for W_scalar based on time series of RH and photosynthetic photon flux density (PPFD) that significantly improved the performance of the VPM. Whether these new functions perform equally well in water stressed and unstressed tropical forests needs to be determined, but presumably unstressed ecosystems would have high cloud cover and humidity, which would minimize variations in W_scalar and GPP to spatial and/or temporal variation in water availability.     

Crystallization and preliminary X-ray diffraction studies of the soluble 14 kDa beta-galactoside-binding lectin from bovine heart

The soluble 14 kDa beta-galactoside-binding lectin from bovine heart, a member of the S-type lectin family, has been crystallized in a form suitable for X-ray diffraction analysis. The crystals, in the absence of a saccharide ligand, diffract beyond 2.5 A resolution. They are obtained from polyethylene glycol 6000 at pH 6.0. Crystals grow as monoclinic plates, space group P2(1), with cell dimensions: a = 35.47 A, b = 64.33 A, c = 58.78 A and beta = 91.7 degrees. The asymmetric unit contains two molecules related by a 2-fold non-crystallographic axis. Two lectin monomers in the asymmetric unit give a Vm of 2.4 A3/Da, i.e. a solvent content of approximately 50%. The complex of lectin with the saccharide ligand, N-acetyllactosamine, crystallizes in the space group P2(1)2(1)2 with cell dimensions: a = 63.55 A, b = 82.13 A and c = 62.39 A. Crystals of this complex diffract beyond 2.0 A resolution. Two complexes in the asymmetric unit lead to a Vm value of 2.8 A3/Da (57% solvent).     

Gluten contamination in food services and industry: A systematic review

Abstract

Gluten-related disorders (GRD) affects approximately 10% of the general population. The only treatment for GRD is still so far is the lifelong complete exclusion of gluten from the daily diet. The correct information about the presence/absence of gluten in food is very important to this group. The present study aimed to evaluate the prevalence of gluten contamination in gluten-free industrial and non-industrial products. In this systematic review, 24 cross-sectional studies were analyzed. The authors developed specific search strategies for Science Direct, Scopus, Web of Science, Google Scholar and ProQuest Dissertations & Theses Global. The authors evaluated the methodological quality of the included studies using criteria from Meta-analysis of Statistics Assessment and Review Instrument (MASTARI). We performed the statistical meta-analysis by metafor package of R program. 95.83% (n?=?23) of the studies presented positive results for contamination (over 20?ppm). In industrial food products, studies showed a contamination prevalence of 13.2% (95% CI: 10.8%–15.7%). In non-industrial food products, studies showed a contamination prevalence of 41.5% (95% CI: 16.6%–66.4%). Despite the non-industrial products presented higher contamination prevalence than the industrial products, the difference was not significant (p?=?0.072). The findings indicate cross-contamination in industrialized and non-industrialized products. As expected, industrial products labeled as gluten-free showed a lower percentage of gluten-contamination than non-industrialized. Despite that, any contaminated sample found in this group present greater relevance than non-labeled foods. It indicates that foods labeled as “gluten-free” should not be considered safe for patients with GRD since information on the label regarding the presence/absence of gluten is unreliable. Therefore, any gluten-contamination in products labeled as gluten-free is a serious problem to whom present GRD. Further studies are needed to estimate gluten cross-contamination in food service meals and industry better.     

Removal of As(V) and Cr(VI) from aqueous solutions using solid waste from leather industry

This study evaluated the feasibility of using a solid waste from the leather industry as an adsorbent for removal of Cr(VI) and As(V) from aqueous media. The adsorbent material was characterized by chemical analyses, infrared spectroscopy, and scanning electronic microscopy (SEM) prior to reaction in order to assess its surface properties. Langmuir and Freundlich equations were used for analyzing the experimental data, which showed a better fit to the Langmuir model, thus suggesting a monolayer adsorption process in the surface of the adsorbent. The high amounts of Cr(VI)-133 mg g(-1) and As(V)-26 mg g(-1) adsorbed demonstrates the great potential for using this solid waste from the leather industry as a low-cost alternative to the traditionally used adsorbent materials.     

Fast intra prediction algorithm based on texture analysis for 3D-HEVC encoders

The advances in display technologies and the growing popularity of 3D video systems have attracted more consumers for 3D viewing experiences, and, consequently, the demand for storage and transmission of 3D video content is increasing. To cope with this demand, a 3D video extension of high-efficiency video coding (HEVC) standard is being developed and near the final standardization stage. The upcoming 3D-HEVC standard is expected to provide higher encoding efficiency than its predecessors, supporting multiple views with high resolution, at a cost of considerable increase in computational complexity, which can be an obstacle to its use in real-time applications. This article proposes a novel complexity reduction algorithm developed to optimize the 3D-HEVC intra mode decision targeting real-time video processing for consumer devices with limited computational power, such as 3D camcorders and smartphones equipped with multiple cameras and depth acquisition capabilities. The proposed algorithm analyzes the texture frames and depth maps to estimate the orientation of edges present in the prediction unit data, speeding up the intra prediction process and reducing the 3D-HEVC encoding processing time. Experimental results demonstrate that the proposed algorithm can save 26 % in computational complexity on average with negligible loss of encoding efficiency. This solution contributes to make more feasible the compression of 3D videos targeting real-time applications in power-constrained devices.     

Complexity via Gold-Catalyzed Molecular Gymnastics

Reactions of 1,6-enynes catalyzed by gold(I) complexes usually proceed stereospecifically through highly distorted cyclopropyl gold carbenes. Substrates with an alkoxy substituent at the propargylic position undergo stereoselective transformations through intermediates in which the OR group and the gold carbene are anti-oriented. Intramolecular attack of carbonyl groups to the cyclopropyl gold carbene is faster than the 1,5-migration of the OR groups, which itself is faster than the intramolecular cyclopropanation by a pendant alkenyl group. The intramolecular attack of carbonyl groups is the key transformation in the [2+2+2] gold-catalyzed cycloaddition, which has been applied in the total synthesis of (+)-orientalol F.     

NMR-measurements for determination of local moisture content of coated wood

Local increased moisture content (MC) in wood constructions may result in different kinds of mechanical and, especially, biological degrading problems. Therefore, it is of great importance to control the MC of the material. However, there is at present no appropriate method for determining local MC in wood without destroying the product itself. Nondestructive measurements of local MC in wood is significant for the possibility of, for instance, monitoring the in situ MC in wood constructions over time, and thereby predicting potential problems. The nuclear magnetic resonance (NMR) technique has been shown to be valuable for the measurement of MC in wood. In this study, the possibility of utilizing this technique for local MC measurement in wood has been tested on wood samples exposed to water absorption for 72 h. The samples came from three different wood species treated with paint systems available on the market. In the wood samples an artificial “crack” had been created in the paint to introduce an area where the water could easily gain access to the wood. The results show the possibility of using the NMR technique for local MC measurements in wood. The measurement area, however, must be related to the properties of the material. In the case of wood, the measurement spot must be related to the early/latewood proportions. Further, a calibration of the NMR measurement must be made in relation to the expected density variations of the material.     

13C NMR study of presence of uron structures in amino adhesives and relation with wood‐based panels performance

The chemical structure of amino adhesives produced by the strongly acid process was investigated by ¹³C Nuclear Magnetic Resonance spectroscopy. This technique allowed the identification of functional groups and its quantitative determination. Concentration of cyclic polymeric structures (urons) was shown to be related with adhesive performance and with particleboard physico‐mechanical properties and formaldehyde content. Higher urons concentration presented lower viscosity and reactivity. Particleboards produced with resins with lower urons concentration presented lower formaldehyde content, but also lower internal bond strength. Wood‐based panels produced fulfilled E1 class requirements for formaldehyde emissions, indicating that strongly acid process is an alternative to the conventional alkaline–acid process. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 4500–4507, 2013     

Esterification of ethenyl benzene and its derivatives with acetic acid in the presence of perchloric acid as a catalyst

The esterification process of ethenyl benzene and its derivative compounds (p-methyl, p-methoxy, p-chloro, m-methyl, m-nitro and m-chloro, respectively) was carried out with acetic acid and using perchloric acid as a catalyst. From the effects of the variables studied it could be concluded that: the temperature and the catalyst concentration influence positively over the olefin conversion, whereas the initial olefin concentration exert no effect over the same; and that the presence of perchloric salts exerts a different influence, depending on the temperature and on the catalyst concentration. It has been proven that the substituted radicals in the m- or p- positions exert an important influence over the conversion of the studied olefins, presenting growing reactivity in the following order: m-nitro ethenyl benzene, m-chloro ethenyl benzene, p-chloro ethenyl benzene, m-methyl ethenyl benzene, ethenyl benzene, p-methyl ethenyl benzene and p-methoxy ethenyl benzene. Finally, a kinetic and thermodynamic study has been done and the corresponding parameters have been calculated, with an adequate fitting.     

Study of the vertical transport in <Emphasis Type="Italic">p</Emphasis>-doped superlattices based on group III-V semiconductors

The electrical conductivity σ has been calculated for p-doped GaAs/Al_0.3Ga_0.7As and cubic GaN/Al_0.3Ga_0.7N thin superlattices (SLs). The calculations are done within a self-consistent approach to the theory by means of a full six-band Luttinger-Kohn Hamiltonian, together with the Poisson equation in a plane wave representation, including exchange correlation effects within the local density approximation. It was also assumed that transport in the SL occurs through extended minibands states for each carrier, and the conductivity is calculated at zero temperature and in low-field ohmic limits by the quasi-chemical Boltzmann kinetic equation. It was shown that the particular minibands structure of the p-doped SLs leads to a plateau-like behavior in the conductivity as a function of the donor concentration and/or the Fermi level energy. In addition, it is shown that the Coulomb and exchange-correlation effects play an important role in these systems, since they determine the bending potential.