239 research outputs found

    Data validation and missing data reconstruction using self-organizing map for water treatment

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    Applications in the water treatment domain generally rely on complex sensors located at remote sites. The processing of the corresponding measurements for generating higher-level information such as optimization of coagulation dosing must therefore account for possible sensor failures and imperfect input data. In this paper, selforganizing map (SOM)-based methods are applied to multiparameter data validation and missing data reconstruction in a drinking water treatment. The SOM is a special kind of artificial neural networks that can be used for analysis and visualization of large high-dimensional data sets. It performs both in a nonlinear mapping from a high-dimensional data space to a low-dimensional space aiming to preserve the most important topological and metric relationships of the original data elements and, thus, inherently clusters the data. Combining the SOM results with those obtained by a fuzzy technique that uses marginal adequacy concept to identify the functional states (normal or abnormal), the SOM performances of validation and reconstruction process are tested successfully on the experimental data stemming from a coagulation process involved in drinking water treatment

    Derived crop coefficients for winter wheat using different reference evpotranspiration estimates methods

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    This paper reports the results of using three empirical methods (Makkink, Priestley-Taylor and Hargreaves) for estimating the reference evapotranspiration (ET0) in the semi-arid region of Tensift Al Haouz, Marrakech (center of Morocco). The Penman-Monteith equation, standardized by the Food and Agriculture Organization (FAO-PM), is used to evaluate the three empirical methods. The obtained ET0 data were used to estimate crop water requirement (ET) of winter wheat using the crop coefficient (K-c) approach and results were compared with ET measured by the Eddy Covariance technique. The result showed that using the original empirical coefficients a, alpha and C-m in Hargreaves, Priestley-Taylor and Makkink equations, respectively, the Hargreaves method agreed fairly well with FAO-PM method at the test site. Conversely, the Priestley-Taylor and Makkink methods underestimate the ET by about 20 and 18 %. After adjustment of the original values of two parameters alpha and C-m coefficients in Priestley-Taylor and Makkink equations, the underestimation of ET was reduced to 9% and 4% for the Priestley Taylor and Makkink methods, respectively, which led to an improvement of 55% and 76% of the obtained values compared with the original values

    Genome-wide footprints in the carob tree (Ceratonia siliqua) unveil a new domestication pattern of a fruit tree in the Mediterranean

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    Intense research efforts over the last two decades have renewed our understanding of plant phylogeography and domestication in the Mediterranean basin. Here we aim to investigate the evolutionary history and the origin of domestication of the carob tree (Ceratonia siliqua), which has been cultivated for millennia for food and fodder. We used >1000 microsatellite genotypes to delimit seven carob evolutionary units (CEUs). We investigated genome-wide diversity and evolutionary patterns of the CEUs with 3557 single nucleotide polymorphisms generated by restriction-site associated DNA sequencing (RADseq). To address the complex wild vs. cultivated status of sampled trees, we classified 56 sampled populations across the Mediterranean basin as wild, seminatural or cultivated. Nuclear and cytoplasmic loci were identified from RADseq data and separated for analyses. Phylogenetic analyses of these genomic-wide data allowed us to resolve west-to-east expansions from a single long-term refugium probably located in the foothills of the High Atlas Mountains near the Atlantic coast. Our findings support multiple origins of domestication with a low impact on the genetic diversity at range-wide level. The carob was mostly domesticated from locally selected wild genotypes and scattered long-distance westward dispersals of domesticated varieties by humans, concomitant with major historical migrations by Romans, Greeks and Arabs. Ex situ efforts to preserve carob genetic resources should prioritize accessions from both western and eastern populations, with emphasis on the most differentiated CEUs situated in southwest Morocco, south Spain and eastern Mediterranean. Our study highlights the relevance of wild and seminatural habitats in the conservation of genetic resources for cultivated trees

    Hepcidin sequesters iron to sustain nucleotide metabolism and mitochondrial function in colorectal cancer epithelial cells

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    Colorectal cancer (CRC) requires massive iron stores, but the complete mechanisms by which CRC modulates local iron handling are poorly understood. Here, we demonstrate that hepcidin is activated ectopically in CRC. Mice deficient in hepcidin specifically in the colon tumour epithelium, compared with wild-type littermates, exhibit significantly diminished tumour number, burden and size in a sporadic model of CRC, whereas accumulation of intracellular iron by deletion of the iron exporter ferroportin exacerbates these tumour parameters. Metabolomic analysis of three-dimensional patient-derived CRC tumour enteroids indicates a prioritization of iron in CRC for the production of nucleotides, which is recapitulated in our hepcidin/ferroportin mouse CRC models. Mechanistically, our data suggest that iron chelation decreases mitochondrial function, thereby altering nucleotide synthesis, whereas exogenous supplementation of nucleosides or aspartate partially rescues tumour growth in patient-derived enteroids and CRC cell lines in the presence of an iron chelator. Collectively, these data suggest that ectopic hepcidin in the tumour epithelium establishes an axis to sequester iron in order to maintain the nucleotide pool and sustain proliferation in colorectal tumours

    Phenylephrine increases cardiac output by raising cardiac preload in patients with anesthesia induced hypotension

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    Induction of general anesthesia frequently induces arterial hypotension, which is often treated with a vasopressor, such as phenylephrine. As a pure -agonist, phenylephrine is conventionally considered to solely induce arterial vasoconstriction and thus increase cardiac afterload but not cardiac preload. In specific circumstances, however, phenylephrine may also contribute to an increase in venous return and thus cardiac output (CO). The aim of this study is to describe the initial time course of the effects of phenylephrine on various hemodynamic variables and to evaluate the ability of advanced hemodynamic monitoring to quantify these changes through different hemodynamic variables. In 24 patients, after induction of anesthesia, during the period before surgical stimulus, phenylephrine 2 mu gkg(-1) was administered when the MAP dropped below 80% of the awake state baseline value for >3min. The mean arterial blood pressure (MAP), heart rate (HR), end-tidal CO2 (EtCO2), central venous pressure (CVP), stroke volume (SV), CO, pulse pressure variation (PPV), stroke volume variation (SVV) and systemic vascular resistance (SVR) were recorded continuously. The values at the moment before administration of phenylephrine and 5(T-5) and 10(T-10)min thereafter were compared. After phenylephrine, the mean(SD) MAP, SV, CO, CVP and EtCO2 increased by 34(13)mmHg, 11(9)mL, 1.02(0.74)Lmin(-1), 3(2.6)mmHg and 4.0(1.6)mmHg at T-5 respectively, while both dynamic preload variables decreased: PPV dropped from 20% at baseline to 9% at T-5 and to 13% at T-10 and SVV from 19 to 11 and 14%, respectively. Initially, the increase in MAP was perfectly aligned with the increase in SVR, until 150s after the initial increase in MAP, when both curves started to dissociate. The dissociation of the evolution of MAP and SVR, together with the changes in PPV, CVP, EtCO2 and CO indicate that in patients with anesthesia-induced hypotension, phenylephrine increases the CO by virtue of an increase in cardiac preload
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