Differences in the Same OMI/MLS Aura Tropospheric Ozone Data Set Published Before and After January 2013

On the website "NASA Goddard Homepage for Tropospheric Ozone", global data of tropospheric ozone obtained from observations of OMI and MLS Aura satellite instruments, are reported. In mid-2013, the data was covering the period between October 2004 and January 2013. Subsequently, in early 2014, the time series was extended until December 2013. At present time, the published series has been extended to December 2014. Analysing this new series, we observed that the data already published to January 2013 had been replaced; not only the missing months of 2013 were added but all the values published since 2004 were recalculated. We present the detected differences in the comparison between common data to both time series (the original, before January 2013, and the new one, currently published on the website). These differences are important considering that they represent the result of the same satellite observation and should be considered when comparing results before/after January 2013, especially when adopting a certain confidence level in the spectral analysis of these data to intraseasonal scale. A warn of caution is suggested in the use of these observations and intercomparison with other values of these and other instruments, because of possible recurrent problems of instrumental calibration.Fil: Cionco, Rodolfo Gustavo. Universidad Tecnológica Nacional; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Agosta Scarel, Eduardo Andres. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Tecnológica Nacional; Argentina. Universidad Nacional de La Plata; ArgentinaFil: Rodriguez, Rubén L.. Universidad Tecnológica Nacional; Argentina. Universidad Nacional de La Plata; ArgentinaFil: Quaranta, Nancy Esther. Universidad Nacional de La Plata; Argentina. Universidad Tecnológica Nacional; Argentin

Differences in the Same OMI/MLS Aura Tropospheric Ozone Data Set Published Before and After January 2013

On the website "NASA Goddard Homepage for Tropospheric Ozone", global data of tropospheric ozone obtained from observations of OMI and MLS Aura satellite instruments, are reported. In mid-2013, the data was covering the period between October 2004 and January 2013. Subsequently, in early 2014, the time series was extended until December 2013. At present time, the published series has been extended to December 2014. Analysing this new series, we observed that the data already published to January 2013 had been replaced; not only the missing months of 2013 were added but all the values published since 2004 were recalculated. We present the detected differences in the comparison between common data to both time series (the original, before January 2013, and the new one, currently published on the website). These differences are important considering that they represent the result of the same satellite observation and should be considered when comparing results before/after January 2013, especially when adopting a certain confidence level in the spectral analysis of these data to intraseasonal scale. A warn of caution is suggested in the use of these observations and intercomparison with other values of these and other instruments, because of possible recurrent problems of instrumental calibration.Facultad de Ciencias Astronómicas y Geofísica

Effective Thermoelectric Power Generation in an Insulated Compartment

The Seebeck coefficient S is a temperature- and material-dependent property, which linearly and causally relates the temperature difference ΔT between the “hot” and “cold” junctions of a thermoelectric power generator (TEC-PG) to the voltage difference ΔV . This phenomenon is the Seebeck effect (SE), and can be used to convert waste heat into usable energy. This work investigates the trends of the effective voltage output ΔV (t ) and effective Seebeck coefficient S′(t ) versus several hours of activity of a solid state TEC-PG device. The effective Seebeck coefficient S′(t ) here is related to a device, not just to a material’s performance. The observations are pursued in an insulated compartment in various geometrical and environmental configurations. The results indicate that the SE does not substantially depend on the geometrical and environmental configurations. However, the effective Seebeck coefficient S′(t ) and the produced effective ΔV (t ) are affected by the environmental configuration, once the temperature is fixed. Heat transfer calculations do not completely explain this finding. Alternative explanations are hypothesized

Variation in the CXCR1 gene (IL8RA) is not associated with susceptibility to chronic periodontitis

<p>Abstract</p> <p>Background</p> <p>The chemokine receptor 1 CXCR-1 (or IL8R-alpha) is a specific receptor for the interleukin 8 (IL-8), which is chemoattractant for neutrophils and has an important role in the inflammatory response. The polymorphism rs2234671 at position Ex2+860G > C of the <it>CXCR1 </it>gene causes a conservative amino acid substitution (S276T). This single nucleotide polymorphism (SNP) seemed to be functional as it was associated with decreased lung cancer risk. Previous studies of our group found association of haplotypes in the <it>IL8 </it>and in the <it>CXCR2 </it>genes with the multifactorial disease chronic periodontitis. In this study we investigated the polymorphism rs2234671 in 395 Brazilian subjects with and without chronic periodontitis.</p> <p>Findings</p> <p>Similar distribution of the allelic and genotypic frequencies were observed between the groups (p > 0.05).</p> <p>Conclusions</p> <p>The polymorphism rs2234671 in the <it>CXCR1 </it>gene was not associated with the susceptibility to chronic periodontitis in the studied Brazilian population.</p

Different contribution of BRINP3 gene in chronic periodontitis and peri-implantitis: A cross-sectional study

Background: Peri-implantitis is a chronic inflammation, resulting in loss of supporting bone around implants. Chronic periodontitis is a risk indicator for implant failure. Both diseases have a common etiology regarding inflammatory destructive response. BRINP3 gene is associated with aggressive periodontitis. However, is still unclear if chronic periodontitis and peri-implantitis have the same genetic background. The aim of this work was to investigate the association between BRINP3 genetic variation (rs1342913 and rs1935881) and expression and susceptibility to both diseases. Methods: Periodontal and peri-implant examinations were performed in 215 subjects, divided into: healthy (without chronic periodontitis and peri-implantitis, n = 93); diseased (with chronic periodontitis and peri-implantitis, n = 52); chronic periodontitis only (n = 36), and peri-implantitis only (n = 34). A replication sample of 92 subjects who lost implants and 185 subjects successfully treated with implants were tested. DNA was extracted from buccal cells. Two genetic markers of BRINP3 (rs1342913 and rs1935881) were genotyped using TaqMan chemistry. Chi-square (p<0.05) compared genotype and allele frequency between groups. A subset of subjects (n = 31) had gingival biopsies harvested. The BRINP3 mRNA levels were studied by CT method (2δδCT). Mann-Whitney test correlated the levels of BRINP3 in each group (p<0.05). Results: Statistically significant association between BRINP3 rs1342913 and peri-implantitis was found in both studied groups (p<0.04). The levels of BRINP3 mRNA were significantly higher in diseased subjects compared to healthy individuals (p<0.01). Conclusion: This study provides evidence that the BRINP3 polymorphic variant rs1342913 and low level of BRINP3 expression are associated with peri-implantitis, independently from the presence of chronic periodontitis

Absence Of Mutations In The Homeodomain Of The Msx1 Gene In Patients With Hypodontia.

Hypodontia, the congenital absence of one or a few permanent teeth, is one of the most frequent alterations of the human dentition. Although hypodontia does not represent a public health problem, it may cause both speech and masticatory dysfunction and esthetic problems. A missense mutation in the homeodomain of MSX1 gene has been associated with hypodontia of second premolars and third molars in humans. However, another study excluded this gene as causative locus for hypodontia of incisors and premolars. To further investigate the role of the MSX1 gene in human hypodontia, we analyzed the homeobox region of the MSX1 gene in 20 individuals with different patterns of familial or isolated hypodontia. The direct sequencing of PCR products did not show any polymorphisms or mutations in the human MSX1 gene. Our results indicate that inactivation of MSX1 gene in humans must have a highly selective effect on dentition, and other genes must be involved in the cause of hypodontia in humans.92346-