Improving the SMAC atmospheric correction code by analysis of Meteosat Second Generation NDVI and surface reflectance data

In order to obtain high quality data, the correction of atmospheric perturbations acting upon land surface reflectance measurements recorded by a space-based sensor is an important topic within remote sensing. For many years the Second Simulation of the Satellite Signal in the Solar Spectrum (6S) radiative transfer model and the Simplified Method for Atmospheric Correction (SMAC) codes have been used for this atmospheric correction, but previous studies have shown that in a number of situations the quality of correction provided by the SMAC is low. This paper describes a method designed to improve the quality of the SMAC atmospheric correction algorithm through a slight increase in its computational complexity. Data gathered from the SEVIRI aboard Meteosat Second Generation (MSG) is used to validate the additions to SMAC, both by comparison to simulated data corrected using the highly accurate 6S method and by comparison to in-situ and 6S corrected SEVIRI data gathered for two field sites in Africa. The additions to the SMAC are found to greatly increase the quality of atmospheric correction performed, as well as broaden the range of atmospheric conditions under which the SMAC can be applied. When examining the Normalised Difference Vegetation Index (NDVI), the relative difference between SMAC and in-situ values decreases by 1.5% with the improvements in place. Similarly, the mean relative difference between SMAC and 6S reflectance values decreases by a mean of 13, 14.5 and 8.5% for Channels 1, 2 and 3 respectively. Furthermore, the processing speed of the SMAC is found to remain largely unaffected, with only a small increase in the time taken to process a full SEVIRI scene. Whilst the method described within this paper is only applicable to SEVIRI data, a similar approach can be applied to other data sources than SEVIRI, and should result in a similar accuracy improvement no matter which instrument supplies the original data.     

Contemporary land use/land cover types determine soil organic carbon stocks in south-west Rwanda

Soil organic carbon (SOC) constitutes a large pool within the global carbon cycle. Land use change significantly drives SOC stock variation. In tropical central and eastern Africa, how changes in land use and land cover impact on soil C stocks remains unclear. Variability in the existing data is typically explained by soil and climate factors with little consideration given to land use and management history. To address this knowledge gap, we classified the current and historical land cover and measured SOC stocks under different land cover, soil group and slope type in the humid zone of south-west Rwanda. It was observed that SOC levels were best explained by contemporary land cover types, and not by soil group, conversion history or slope position, although the latter factors explained partly the variation within annual crop land cover type. Lack of the influence of land use history on SOC stocks suggests that after conversion to a new land use/land cover, SOC stocks reached a new equilibrium within the timestep that was observed (25 years). For conversion to annual crops, SOC stocks reach a new equilibrium at about 2.5 % SOC concentration which is below the proposed soil fertility threshold of 3 % SOC content in the Eastern and central African region. SOC stock declined under transitions from banana-coffee to annual crop by 5 % or under transitions from natural forest to degraded forest by 21 % and increased for transitions from annual crops to plantation forest by 193 %. Forest clearing for agricultural use resulted in a loss of 72 %. Assuming steady states, the data can also be used to make inferences about SOC changes as a result of land cover changes. We recommend that SOC stocks should be reported by land cover type rather than by soil groups which masks local land cover and landscape differences. This study addresses a critical issue on sustainable management of SOC in the tropics and global carbon cycle given that it is performed in a part of the world that has high land cover dynamics while at the same time lacks data on land cover changes and SOC dynamics.     

Drosophila acetylcholinesterase: mechanisms of resistance to organophosphates

Quantitative and qualitative changes of acetylcholinesterase can affect the sensitivity of insects to insecticides. First, the amount of acetylcholinesterase in the central nervous system is important in Drosophila melanogaster, flies which overexpress the enzyme are more resistant than wild-type flies. On the contrary, flies which express low levels of acetylcholinesterase are more susceptible. An overproduction of acetylcholinesterase outside the central nervous system also protects against organophosphate poisoning, that is, flies producing a soluble acetylcholinesterase, secreted in the haemolymph, are resistant to organophosphates. Second, resistance can also result from a qualitative modification of acetylcholinesterase. Four mutations have been identified in resistant strains: Phe115 to Ser, Ileu199 to Val, Gly303 to Ala and Phe368 to Tyr. Each of these mutations led to a different pattern of resistance and combinations between these mutations led to highly resistant enzymes.     

Splicing of 5' introns dictates alternative splice selection of acetylcholinesterase pre-mRNA and specific expression during myogenesis

Splicing of alternative exon 6 to invariant exons 2, 3, and 4 in acetylcholinesterase (AChE) pre-mRNA results in expression of the prevailing enzyme species in the nervous system and at the neuromuscular junction of skeletal muscle. The structural determinants controlling splice selection are examined in differentiating C2-C12 muscle cells by selective intron deletion from and site-directed mutagenesis in the Ache gene. Transfection of a plasmid lacking two invariant introns (introns II and III) within the open reading frame of the Ache gene, located 5' of the alternative splice region, resulted in alternatively spliced mRNAs encoding enzyme forms not found endogenously in myotubes. Retention of either intron II or III is sufficient to control the tissue-specific pre-mRNA splicing pattern prevalent in situ. Further deletions and branch point mutations revealed that upstream splicing, but not the secondary structure of AChE pre-mRNA, is the determining factor in the splice selection. In addition, deletion of the alternative intron between the splice donor site and alternative acceptor sites resulted in aberrant upstream splicing. Thus, selective splicing of AChE pre-mRNA during myogenesis occurs in an ordered recognition sequence in which the alternative intron influences the fidelity of correct upstream splicing, which, in turn, determines the downstream splice selection of alternative exons.     

Use of к-carrageenan,chitosan and Carbopol 974P in extruded and spheronized pellets that are devoid of MCC

The search for excipients to replace microcrystalline cellulose (MCC) in the production of pellets by extrusion-spheronization in cases of drug incompatibility or the lack of pellet matrix disintegration forms the basis of this study. A combination of к-carrageenan as a spheronization aid, chitosan as a diluent and Carbopol^® 974P as a binder in the production of pellets containing no MCC has been investigated using acetaminophen as a model drug. Design of experiments allowed assessment of formulation and processing effects on pellet responses that included size, shape, fines, yield and friability. Statistical analysis revealed that the main factors and some of the two-factor interactions had a significant effect on pellet characteristics. Formulations containing high levels of к-carrageenan required more water to produce a wetted mass with good extrudability and extrudate capable of being spheronized. Although only a low level of Carbopol was used in the formulation, it imparted cohesiveness to the wetted mass as well as the extrudate. Furthermore, it was discovered that Carbopol could act as an extrusion aid, enabling the wetted mass to flow easily through the extruder screen holes without building up heat. Spherical and rugged pellets were produced that met the immediate release criterion.     

Insights into remediation technology for malachite green wastewater treatment

Malachite green (MG) dye is a common industrial dye and organic contaminant that can be found in (waste)water. Textile and food industries make use of MG as dyeing and food coloring agents, respectively. However, MG is both genotoxic and mutagenic. Hence, the elimination of MG from MG-laden-wastewater is germane. This review summarizes up-to-date researches that have been reported in literature as regards the decontamination of toxic MG wastewater. Various removal methods (adsorption, membrane, Fenton system, and heterogenous and homogeneous photodegradation) were discussed. Of the two basic technologies that are comprehensively explored and reviewed, chemical treatment methods are not as viable as physical removal methods, such as the adsorption technology, due to the lack of secondary pollutant production, simple design, low operation costs, and resource availability. This review also presents various practical knowledge gaps needed for large-scale applications of adsorptive removal methods for MG. It concludes by recommending further research on the techniques of cheap and simple decontamination of MG to get clean water.     

Orientation Polarization Spectroscopy—Toward an Atomistic Understanding of Dielectric Relaxation Processes

The theory of orientation polarization and dielectric relaxation was developed by P. Debye more than 100 years ago. It is based on approximating a molecule by a sphere having one or more dipole moments. By that the detailed intra- and intermolecular interactions are explicitly not taken into consideration. In this article, the principal limitations of the Debye approximation are discussed. Taking advantage of the molecular specificity of the infrared (IR) spectral range, measurements of the specific IR absorption of the stretching vibration υ(OH) (at 3370 cm⁻¹) and the asymmetric υ_as(CH₂) (at 2862.9 cm⁻¹) are performed in dependence on the frequency and the strength of external electric fields and at varying temperature. The observed effects are interpreted as caused by orientation polarization of the OH and the adjacent CH₂ moieties.