Factors influencing fluffy layer suspended matter (FLSM) properties in the Odra River - Pomeranian Bay - Arkona Deep System (Baltic Sea) as derived by principal components analysis (PCA), and cluster analysis (CA)

Factors conditioning formation and properties of suspended matter resting on the sea floor (Fluffy Layer Suspended Matter - FLSM) in the Odra river mouth - Arkona Deep system (southern Baltic Sea) were investigated. <P style='line-height: 20px;'> Thirty FLSM samples were collected from four sampling stations, during nine cruises, in the period 1996-1998. Twenty six chemical properties of the fluffy material were measured (organic matter-total, humic substances, a variety of fatty acids fractions, P, N, &delta;13C, &delta;15N; Li; heavy metals- Co, Cd, Pb, Ni, Zn, Fe, Al, Mn, Cu, Cr). The so obtained data set was subjected to statistical evaluation. <P style='line-height: 20px;'> Comparison of mean values of the measured properties led to conclusion that both seasonal and spatial differences of the fluffy material collected at the stations occured. Application of Principal Component Analysis, and Cluster Analysis, to the data set amended with environmental characteristics (depth, salinity, chlorophyll <i>a</i>, distance from the river mouth), led to quantification of factors conditioning the FLSM formation. The five most important factors were: contribution of the lithogenic component (responsible for 25% of the data set variability), time dependent factors (including primary productivity, mass exchange with fine sediment fraction, atmospheric deposition, contribution of material originating from abrasion-altogether 21%), contribution of fresh autochtonous organic matter (9%), influence of microbial activity (8%), seasonality (8%)

The Antioxidant 3H-1,2-Dithiole-3-Thione Potentiates Advanced Glycation End-Product-Induced Oxidative Stress in SH-SY5Y Cells

Oxidative stress is implicated as a major factor in the development of diabetes complications and is caused in part by advanced glycation end products (AGEs). AGEs ligate to the receptor for AGEs (RAGE), promoting protein kinase C (PKC)-dependent activation of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase and superoxide radical generation. While scavenging antioxidants are protective against AGEs, it is unknown if induction of endogenous antioxidant defenses has the same effect. In this study, we confirmed that the compound 3H-1,2-dithiole-3-thione (D3T) increases reduced-state glutathione (GSH) concentrations and NADPH:quinone oxidoreductase 1 (NQO1) activity in SH-SY5Y cells and provides protection against H2O2. Surprisingly, D3T potentiated oxidative damage caused by AGEs. In comparison to vehicle controls, D3T caused greater AGE-induced cytotoxicity and depletion of intracellular GSH levels while offering no protection against neurite degeneration or protein carbonylation. D3T potentiated AGE-induced reactive oxygen species (ROS) formation, an effect abrogated by inhibitors of PKC and NADPH oxidase. This study suggests that chemical induction of endogenous antioxidant defenses requires further examination in models of diabetes

Public Transport to the Airport and Its Influence on Handling Process

The paper focuses on several possibilities of the mass public transport to the airport, including analyses of the expected impact on the various airport processes. Within the article, three main transportation system types will be described and compared. Firstly, the problem regarding current bus transfer system to the Václav Havel airport Prague will be analyzed. According to the analysis results the focus now turns to the description of the potential influence of the introduction of the new transfer systems, including the impact on the airport security and passport control process, and other procedures, which include some kind of a queuing process. This airport was chosen as the biggest airport in the Czech Republic, which in today and future business environment could expect problems related to the public transport of the passengers to and from the airport. Besides the description of the current structure, the paper tries to elaborate issues such as calculation of the queue waiting times and to propose a new system, more suitable for the given conditions. Results of the research include various calculations, such dependence of a modal split and intervals of the waiting times within a check-in process

Podpis w postępowaniu administracyjnem

Digitalizacja i deponowanie archiwalnych zeszytów RPEiS sfinansowane przez MNiSW w ramach realizacji umowy nr 541/P-DUN/201

Quantitative trait mapping in Diversity Outbred mice identifies novel genomic regions associated with the hepatic glutathione redox system.

The tripeptide glutathione (GSH) is instrumental to antioxidant protection and xenobiotic metabolism, and the ratio of its reduced and oxidized forms (GSH/GSSG) indicates the cellular redox environment and maintains key aspects of cellular signaling. Disruptions in GSH levels and GSH/GSSG have long been tied to various chronic diseases, and many studies have examined whether variant alleles in genes responsible for GSH synthesis and metabolism are associated with increased disease risk. However, past studies have been limited to established, canonical GSH genes, though emerging evidence suggests that novel loci and genes influence the GSH redox system in specific tissues. The present study marks the most comprehensive effort to date to directly identify genetic loci associated with the GSH redox system. We employed the Diversity Outbred (DO) mouse population, a model of human genetics, and measured GSH and the essential redox cofactor NADPH in liver, the organ with the highest levels of GSH in the body. Under normal physiological conditions, we observed substantial variation in hepatic GSH and NADPH levels and their redox balances, and discovered a novel, significant quantitative trait locus (QTL) on murine chromosome 16 underlying GSH/GSSG; bioinformatics analyses revealed Socs1 to be the most likely candidate gene. We also discovered novel QTL associated with hepatic NAD