1,667 research outputs found

    Models in geomorphology- Quaternary evolution of the actual relief pattern of coastal central and northern Namib desert

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    Main articleField and laboratory results gained at various SWA/Namibian sites between the Kuiseb river in the south and the Unjab river in the north are presented. At the Namib coast under study two low stands of sea level and two high stands, one of them of Intra-Wurmian age, can be proved. From Toscanini northward a third (? Holocene) high stand exists besides the other two. The former shore lines can be linked spatially and temporally to the terrestrial relief sequences by means of fluvial and eolian land forms and sediments. Thus the changing patterns of more arid or more humid environments at different morphoclimatic stages up to the present one can be described. Furthermore, it is evident that the geomorphic processes themselves change regionally, and it is seen that the Central Namib desert is a geomorphologically unique area in comparison with the Skeleton Coast and the southern dune area. Finally, the tendencies of Quaternary landscape evolution even enable us to deduce some geoecological consequences concerning man's activities in this desert.Deutsche Forschungsgemeinschaf

    Impact assessment of rehabilitation intervention in the Gal Oya Left Bank [Sri Lanka].

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    Irrigation managementWater managementIrrigation systemsProductivityRehabilitationModelsProject evaluationRainReservoir storage

    Tauroursodeoxycholic acid exerts anticholestatic effects by a cooperative cPKC alpha-/PKA-dependent mechanism in rat liver.

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    Objective: Ursodeoxycholic acid (UDCA) exerts anticholestatic effects in part by protein kinase C (PKC)-dependent mechanisms. Its taurine conjugate, TUDCA, is a cPKCa agonist. We tested whether protein kinase A (PKA) might contribute to the anticholestatic action of TUDCA via cooperative cPKCa-/PKA-dependent mechanisms in taurolithocholic acid (TLCA)-induced cholestasis. Methods: In perfused rat liver, bile flow was determined gravimetrically, organic anion secretion spectrophotometrically, lactate dehydrogenase (LDH) release enzymatically, cAMP response-element binding protein (CREB) phosphorylation by immunoblotting, and cAMP by immunoassay. PKC/PKA inhibitors were tested radiochemically. In vitro phosphorylation of the conjugate export pump, Mrp2/Abcc2, was studied in rat hepatocytes and human Hep-G2 hepatoma cells. Results: In livers treated with TLCA (10 mmol/l)+TUDCA (25 mmol/l), combined inhibition of cPKC by the cPKCselective inhibitor Go¨6976 (100 nmol/l) or the nonselective PKC inhibitor staurosporine (10 nmol/l) and of PKA by H89 (100 nmol/l) reduced bile flow by 36% (p,0.05) and 48% (p,0.01), and secretion of the Mrp2/ Abcc2 substrate, 2,4-dinitrophenyl-S-glutathione, by 31% (p,0.05) and 41% (p,0.01), respectively; bile flow was unaffected in control livers or livers treated with TUDCA only or TLCA+taurocholic acid. Inhibition of cPKC or PKA alone did not affect the anticholestatic action of TUDCA. Hepatic cAMP levels and CREB phosphorylation as readout of PKA activity were unaffected by the bile acids tested, suggesting a permissive effect of PKA for the anticholestatic action of TUDCA. Rat and human hepatocellular Mrp2 were phosphorylated by phorbol ester pretreatment and recombinant cPKCa, nPKCe, and PKA, respectively, in a staurosporine-sensitive manner. Conclusion: UDCA conjugates exert their anticholestatic action in bile acid-induced cholestasis in part via cooperative post-translational cPKCa-/PKA-dependent mechanisms. Hepatocellular Mrp2 may be one target of bile acid-induced kinase activation

    A spatial and seasonal climatology of extreme precipitation return-levels: A case study

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    A spatial and seasonal modeling approach for precipitation extremes is introduced and exemplified for the Berlin-Brandenburg region in Germany. Monthly maxima of daily precipitation sums are described with a generalized extreme value distribution (GEV) with spatially and seasonally varying parameters. This allows for a return-level prediction also at ungauged sites. The seasonality is captured with harmonic functions, spatial variations are modeled with Legendre polynomials for longitude, latitude and altitude. Interactions between season and space allow for a spatially varying seasonal cycle. Orders of the harmonic and Legendre series are determined using a step-wise forward regression approach with the Bayesian Information Criterion (BIC) as model selection criterion. The longest 80 series are used to verify the approach in a cross-validation experiment based on the Quantile Skill Score (QSS). The model presented describes the observations at all these stations more accurately than a GEV applied to each month and location separately. These improvements are due to the assumption of smoothly varying GEV parameters in time and space; information from neighboring observations in time and space are used to obtain parameters at a given location. Apart from robustness, this approach allows also a seasonally and spatially varying shape parameter and results are found to be more accurate

    Seasonal Cycle in German Daily Precipitation Extremes

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    The seasonal cycle of extreme precipitation in Germany is investigated by fitting statistical models to monthly maxima of daily precipitation sums for 2,865 rain gauges. The basis is a non-stationary generalized extreme value (GEV) distribution variation of location and scale parameters. The negative log-likelihood serves as the forecast error for a cross validation to select adequate orders of the harmonic functions for each station. For nearly all gauges considered, the seasonal model is more appropriate to estimate return levels on a monthly scale than a stationary GEV used for individual months. The 100-year return-levels show the influence of cyclones in the western, and convective events in the eastern part of Germany. In addition to resolving the seasonality, we use a simulation study to show that annual return levels can be estimated more precisely from a monthly-resolved seasonal model than from a stationary model based on annual maxima

    Control of the charge state of metal atoms on thin MgO films

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    Biliary Bicarbonate Secretion Constitutes a Protective Mechanism against Bile Acid-Induced Injury in Man

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    Background: Cholangiocytes expose a striking resistance against bile acids: while other cell types, such as hepatocytes, are susceptible to bile acid-induced toxicity and apoptosis already at micromolar concentrations, cholangiocytes are continuously exposed to millimolar concentrations as present in bile. We present a hypothesis suggesting that biliary secretion of HCO(3)(-) in man serves to protect cholangiocytes against bile acid-induced damage by fostering the deprotonation of apolar bile acids to more polar bile salts. Here, we tested if bile acid-induced toxicity is pH-dependent and if anion exchanger 2 (AE2) protects against bile acid-induced damage. Methods: A human cholangiocyte cell line was exposed to chenodeoxycholate (CDC), or its glycine conjugate, from 0.5 mM to 2.0 mM at pH 7.4, 7.1, 6.7 or 6.4, or after knockdown of AE2. Cell viability and apoptosis were determined by WST and caspase-3/-7 assays, respectively. Results: Glycochenodeoxycholate (GCDC) uptake in cholangiocytes is pH-dependent. Furthermore, CDC and GCDC (pK(a) 4-5) induce cholangiocyte toxicity in a pH-dependent manner: 0.5 mM CDC and 1 mM GCDC at pH 7.4 had no effect on cell viability, but at pH 6.4 decreased viability by >80% and increased caspase activity almost 10- and 30-fold, respectively. Acidification alone had no effect. AE2 knockdown led to 3- and 2-fold enhanced apoptosis induced by 0.75 mM CDC or 2 mM GCDC at pH 7.4. Discussion: These data support our hypothesis of a biliary HCO(3)(-) umbrella serving to protect human cholangiocytes against bile acid-induced injury. AE2 is a key contributor to this protective mechanism. The development and progression of cholangiopathies, such as primary biliary cirrhosis, may be a consequence of genetic and acquired functional defects of genes involved in maintaining the biliary HCO(3)(-) umbrella. Copyright (C) 2011 S. Karger AG, Base
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