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  • 1
    Keywords: Bericht ; Gewässerschutz ; Stadtplanung
    Description / Table of Contents: Die Gewässer in unseren Städten erfüllen vielfältige Funktionen und unterliegen multifunktionalen Ansprüchen mit hohem Nutzungsdruck, was sich nur durch Kooperation aller Beteiligten lösen lässt. Dafür bedarf es neuer Methoden unter Beachtung der komplexen funktionalen Abhängigkeiten. Im Bericht werden die entwickelten Methoden und Ergebnisse aus dem BMBF-Projekt KOGGE vorgestellt, u.a. zur integralen Gewässerentwicklungsplanung. Das methodische Vorgehen wird beispielhaft für die Stadt Rostock illustriert und lässt sich auf ähnliche Fragestellungen in anderen Regionen Deutschlands übertragen.〈ger〉
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource (203 Seiten, 38,90 MB) , Illustrationen, Diagramme, Karten (überwiegend farbig)
    Series Statement: Schriftenreihe Umweltingenieurwesen Band 81
    DDC: 333.7
    RVK:
    Language: German
    Note: "Das Verbundprojekt "KOGGE: Kommunale Gewässer gemeinschaftlich entwickeln" wurde vom Bundesministerium für Bildung und Forschung (BMBF) im Rahmen der Fördermaßnahme "Regionales Wasserressourcen-Management für den nachhaltigen Gewässerschutz in Deutschland" (ReWaM) gefördert (Förderkennzeichen: 033W032A). Laufzeit: 01.04.2015-30.09.2018" - Seite 3 , Verbundnummer 01157605
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  • 2
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Biology-Mathematical models. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (262 pages)
    Edition: 1st ed.
    ISBN: 9780128195963
    DDC: 570.15118
    Language: English
    Note: Front Cover -- Exploring Mathematical Modeling in Biology Through Case Studies and Experimental Activities -- Copyright -- Contents -- Preface -- Tips for using this text - instructors -- Tips for using this text - students -- Online resources -- Acknowledgments -- 1 Preliminaries: models, R, and lab techniques -- 1.1 Bringing mathematics and biology together through modeling -- 1.2 R basics -- 1.2.1 RStudio layout -- 1.2.2 Simple calculations -- 1.2.3 Data structures -- Vectors -- Matrices -- Data frames -- 1.2.4 Basic plotting -- 1.2.5 Reading data from les -- 1.2.6 Iteration -- 1.2.7 Fitting a linear regression model -- 1.3 Prelab lab: practicing the fundamentals -- Introduction -- Materials -- Using the micropipettes -- Serial dilution with dye solutions and water -- Measuring absorbance -- Graphing and data analysis -- 2 Introduction to modeling using difference equations -- 2.1 Discrete-time models -- 2.1.1 Solutions to rst-order difference equations -- 2.1.2 Using linear regression to estimate parameters -- 2.2 Putting it all together: the whooping crane -- 2.3 Case study 1: Island biogeography -- 2.3.1 Background -- 2.3.2 Model formulation -- 2.3.3 Rakata story -- Data -- Parameter estimation -- Model analysis -- 2.3.4 Modern approach: lineage data -- Model -- Parameter estimation -- Model analysis -- 2.3.5 Back to MacArthur and Wilson: effects of distance and area -- 2.4 Case study 2: Pharmacokinetics model -- 2.4.1 Background -- Pharmacokinetics: basic concepts and terminology -- Caffeine -- 2.4.2 Formulating the model -- 2.4.3 Understanding the model -- 2.4.4 Parameter estimation -- 2.4.5 Model evaluation/analysis -- 2.4.6 Further exploration -- 2.5 Case study 3: Invasive plant species -- 2.5.1 Background -- 2.5.2 Model formulation -- 2.5.3 Parameter estimation -- 2.5.4 Model predictions -- 2.5.5 Management strategies. , 2.6 Wet lab: logistic growth model of bacterial population dynamics -- 2.6.1 Introduction -- 2.6.2 Modeling populations -- 2.6.3 The experiment -- Preparation -- Measuring growth rates by optical density -- Measuring growth rate by serial dilution and plate count -- 2.6.4 Model calibration and analysis -- 2.6.5 Experiment part 2: effect of changing media -- 3 Differential equations: model formulation, nonlinear regression, and model selection -- 3.1 Biological background -- 3.2 Mathematical and R background -- 3.2.1 Differential equation-based model formulation -- Constant ow rate -- Relative rates -- Mass action -- Feedback -- 3.2.2 Solutions to ordinary differential equations -- 3.2.3 Investigating parameter space -- 3.2.4 Nonlinear tting -- 3.3 Model selection -- 3.4 Case study 1: How leaf decomposition rates vary with anthropogenic nitrogen deposition -- 3.4.1 Background -- 3.4.2 The data -- 3.4.3 Model formulation -- 3.4.4 Parameter estimation -- 3.4.5 Model evaluation -- 3.5 Case study 2: Exploring models to describe tumor growth rates -- 3.5.1 Background -- 3.5.2 The data -- 3.5.3 Model formulation -- 3.5.4 Parameter estimation -- 3.5.5 Model evaluation: descriptive power -- 3.5.6 Model evaluation: predictive power -- 3.6 Case study 3: Predator responses to prey density vary with temperature -- 3.6.1 Background -- Can predator-prey interactions predict invasive behavior? -- 3.6.2 Analysis of functional response data: determining the parameters -- 3.6.3 Exploring functional responses as a function of temperature -- 3.7 Wet lab: enzyme kinetics of catechol oxidase -- 3.7.1 Overview of activities -- 3.7.2 Introduction to enzyme catalyzed reaction kinetics -- 3.7.3 Deriving the model -- 3.7.4 Estimating KM and Vmax -- 3.7.5 Our enzyme: catechol oxidase -- 3.7.6 Experiment: collecting initial rates for the Michaelis-Menten model. , Overview of the procedure -- Materials -- Enzyme preparation -- Running the reactions -- Analysis in R -- 3.7.7 Effects of inhibitors on enzyme kinetics -- 3.7.8 Experiment: measuring the effects of two catechol oxidase inhibitors, phenylthiourea and benzoic acid -- Analysis in R -- 4 Differential equations: numerical solutions, model calibration, and sensitivity analysis -- 4.1 Biological background -- 4.2 Mathematical and R background -- 4.2.1 Numerical solutions to differential equations -- Example: logistic growth (one variable) -- Example: tumor growth model (a system of two differential equations) -- 4.2.2 Calibration: tting models to data -- Example: calibrating the logistic growth model -- 4.2.3 Sensitivity analysis -- Global sensitivity -- Local sensitivity analysis -- Local sensitivity example: logistic model -- 4.2.4 Putting it all together: the dynamics of Ebola virus infecting cells -- Numerical solution for the Ebola model -- Fitting parameters to the Ebola model: calibrating the model -- Local sensitivity analysis: assessing key parameters in the Ebola virus-cell system -- 4.3 Case study 1: Modeling the 2009 in uenza pandemic -- 4.3.1 Background -- 4.3.2 The SIR model -- Model simulations -- 4.3.3 Cumulative number of cases -- 4.3.4 Epidemic threshold -- 4.3.5 Public health interventions -- 4.3.6 2009 H1N1 in uenza pandemic -- Estimating parameters -- Taking action -- 4.4 Case study 2: Optimizing immunotherapy in prostate cancer -- 4.4.1 Background -- 4.4.2 Model formulation -- 4.4.3 Model implementation -- 4.4.4 Parameter estimation -- 4.4.5 Vaccination protocols and model predictions -- 4.4.6 Sensitivity analysis -- 4.4.7 Simulating other treatment strategies -- 4.5 Case study 3: Quorum sensing -- 4.5.1 Introduction -- 4.5.2 Model formulation -- 4.5.3 Parameter estimation -- 4.5.4 Model simulations -- 4.5.5 Sensitivity analysis. , The temporal response -- 4.6 Wet lab: hormones and homeostasis-keeping blood glucose concentrations stable -- 4.6.1 Overview of activities -- 4.6.2 Introduction to blood glucose regulation and its importance -- 4.6.3 Developing a model -- 4.6.4 Experiment: measuring blood glucose concentrations following glucose ingestion -- Introduction to the procedure -- Experimental procedure -- 4.6.5 Analysis -- 4.6.6 Thoughts to consider for potential follow-up experiments -- 5 Technical notes for laboratory activities -- 5.1 Introduction -- 5.2 Population growth -- Bacterial growth media and tips -- Optional plate counts and converting optical density to numbers of bacteria -- Alternate organisms -- 5.3 Enzyme kinetics -- Tips and solution preparation for catechol oxidase -- Notes on data analysis -- 5.3.1 Notes on other enzymes or similar experiments -- Predator-prey or the enzyme game -- Other enzymes -- 5.4 Blood glucose monitoring -- 5.4.1 Tips for glucose monitoring -- Example of a subject consent form -- 5.4.2 Other lab activities -- Bibliography -- Index -- Back Cover.
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 27 (1988), S. 1695-1703 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 27 (1988), S. 2839-2846 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    [s.l.] : Macmillan Magazines Ltd.
    Nature 388 (1997), S. 416-416 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] SirThe European Molecular Biology Organisation (EMBO) is one of the organizations that award postdoctoral fellowships in molecular biology. The fellowships are funded by the 21 member states of the European Molecular Biology Conference (EMBC). Recipients have to move to a ...
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Molecular and cellular biochemistry 136 (1994), S. 11-22 
    ISSN: 1573-4919
    Keywords: magnesium ; calcium ; mag-fura-2 ; fura-2 ; magnesium regulation ; BC3H-1 cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract The magnesium buffer coefficient (B Mg) was calculated for BC3H-1 cells from the rise in cytosolic Mg2+ activity observed when magnesium was released from ATP after iodoacetate (IAA) and NaCN treatment. The basal cytosolic Mg2+ activity (0.54±0.1 mM) measured with mag-fura-2 doubled when 4.54 mM magnesium was liberated from ATP:B Mg was 12.9 indicating that a 1 mM increase in Mg2+ activity requires an addition of about 13 mM magnesium. The accuracy of this value depends on these assumptions: (a) all of the magnesium released from ATP stayed in the cells; (b) the rise in Mg2+ was not secondary to pH-induced changes inB Mg; (c) mag-fura-2 measured Mg2+ and not Ca2+; and (d) the accuracy of the mag-fura-2 calibration. Total magnesium did not change in response to IAA/CN treatment, thus the change in Mg2+ activity reflected a redistribution of cell magnesium. pH changes induced by NH4Cl pulse and removal had little effect on Mg2+ activity and the changes were slower than and opposite to pH-induced changes in Ca2+ activity measured by fura-2. Ca2+ responses were temporally uncopled from Mg2+ responses when the cells were treated with IAA only and in no cases did Ca2+ levels rise above 1 μM, showing that the mag-fura-2 is responding to Mg2+. Additional studies demonstrated that ∼90% of the mag-fura-2 signal was cytosolic in origin. The remaining non-diffusible mag-fura-2 either was bound to cytosolic membranes or sequestered in organelles with the fluorescence characteristics of the Mg2+-complexed form, even when cytosolic free Mg2+ activity was approximately 0.5 mM. This bound mag-fura-2 would appear to increase the Kd and thus clearly limits the accuracy of our estimmate forB Mg. Despite this limitation, we demonstrate that Mg2+ is tightly regulated in face of large changes in extracellular Mg2+, and that the interplay observed between pH, Ca2+ and Mg2+ activities strongly supports the hypothesis that these factors interact through a shared buffer capacity of the cell.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1573-4919
    Keywords: reconstitution ; lipid vesicles ; surfactants ; micelles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Most structural and functional studies of membrane proteins eventually require that the protein be solubilized from its original membrane, isolated and reconstituted into a membrane composed of native or specific phospholipids. The conditions comprising a successful reconstitution protocol often seem both arbitrary and elusive. The solubilization steps as the neutral surfactant octyl glucoside (OG) is added to the negatively charged lipid phosphatidylserine (PS) were followed by several optical techniques. Vesicle leakage, changes in resonance energy transfer between lipid probes and micelle formation were determined as a function of (PS) and temperature. The (OG) needed at these transitions was linear with (PS) so that average compositions and the free (OG) could be calculated for each point. More OG is needed to solubilize at 15 compared to 35° C reflecting the temperature dependence of pure OG solubility. Although similar, the average compositions of the mixed surfactant-lipid structure and their temperature dependence were not identical to similar points determined for egg phosphatidylcholine and OG.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    The journal of membrane biology 56 (1980), S. 65-72 
    ISSN: 1432-1424
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary Diffusion of auxin (indole-3-acetic acid) through planar lipid bilayer membranes was studied as a function of pH and auxin concentration. Membranes were made of egg or soybean lecithin or phosphatidyl serine inn-decane (25–35 mg/ml). Tracer and electrical techniques were used to estimate the permeabilities to nonionized (HA) and ionized (A−) auxin. The auxin tracer flux is unstirred layer limited at low pH and membrane limited at high pH, i.e., when [A−]≫[HA]. The tracer flux is not affected by the transmembrane voltage and is much higher than the flux predicted from the membrane conductance. Thus, only nonionized auxin crosses the membrane at a significant rate. Auxin transport shows saturation kinetics, but this is due entirely to unstirred layer effects rather than to the existence of an auxin “carrier” in the membrane. A rapid interconversion of A− and HA at the membrane surface allows A− to “facilitate” the auxin flux through the unstirred layer. Thus, the total flux is higher than that expected for the simple diffusion of HA alone. The relation between flux (J A), concentrations and permeabilities is: 1/J A=1/P UL([A−]+[HA])+1/P HA M [HA]. By fitting this equation to our data we find thatP UL=6.9×10−4 cm/sec andP HA M =3.3×10−3 cm/sec for egg lecithin-decane bilayers. Similar membrane permeabilities were observed with phosphatidyl serine or soybean lipids. Thus, auxin permeability is not affected by a net surface charge on the membrane. Our model describing diffusion and reaction in the unstirred layers can explain the “anomolous” relationship between pH and weak acid (or weak base) uptake observed in many plant cells.
    Type of Medium: Electronic Resource
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