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  • 1
    Publication Date: 2015-08-23
    Description: Spreading of conservative solutes in groundwater due to aquifer heterogeneity is quantified by the macrodispersivity, which was found to be scale dependent. It increases with travel distance, stabilizing eventually at a constant value. However, the question of its asymptotic behaviour at very large scale is still a matter of debate. It was surmised in the literature that macrodispersivity scales up following a unique scaling law. Attempts to define such a law were made by fitting a regression line in the log-log representation of an ensemble of macrodispersivities from multiple experiments. The functional relationships differ among the authors, based on the choice of data. Our study revisits the data basis, used for inferring unique scaling, through a detailed analysis of literature marcodispersivities. In addition, values were collected from the most recent tracer tests reported in the literature. We specified a system of criteria for reliability and re-evaluated the reliability of the reported values. The final collection of reliable estimates of macrodispersivity does not support a unique scaling law relationship. On the contrary, our results indicate, that the field data can be explained as a collection of macrodispersivities of aquifers with varying degree of heterogeneity where each exhibits its own constant asymptotic value. Our investigation concludes that transport, and particularly the macrodispersivity, is formation-specific, and that modeling of transport cannot be relegated to a unique scaling law. Instead, transport requires characterization of aquifer properties, e.g. spatial distribution of hydraulic conductivity, and the use of adequate models. This article is protected by copyright. All rights reserved.
    Print ISSN: 0043-1397
    Electronic ISSN: 1944-7973
    Topics: Architecture, Civil Engineering, Surveying , Geography
    Published by Wiley on behalf of American Geophysical Union (AGU).
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  • 2
    Publication Date: 2015-09-17
    Description: Predicting hydro(geo)logical or environmental systems is subject to high levels of uncertainties, especially if appropriate data for model calibration are lacking. For subsurface systems, where data acquisition is cost intensive and time demanding, it is especially important to collect only those data that provide the largest amount of relevant information. The high expenses call for optimal experimental design, which is widely recognized for maximizing the efficiency of experiments. In model-based design of experiments, the analysis of the design efficiency and the resulting optimal design are based on the initial state of knowledge about the modeled system. Joint optimization of multi-measurement designs is a well known challenge and the usefulness of global optimization approaches is widely recognized in this context. However, we will show that the benefit for such global optimization becomes questionable when measurement data become available sequentially. Instead, the optimization effort should be invested within an interactive design approach. Today's fast telecommunication, global connectivity and high-performance computing allow to consider such interactive coupling. This study will use a synthetic case study to compare the standard en-bloc global optimization approach to two interactive design approaches. The approaches are implemented in a Bayesian framework and are compared based on their complexity and overall performance. The key conclusion confirms a previously untested presumption: for models that trigger nonlinear parameter inference problems, interaction (which may come at a loss of global optimization) is more beneficial than global optimization based on the initial state of knowledge (which typically implies the impossibility of interactivity). This article is protected by copyright. All rights reserved.
    Print ISSN: 0043-1397
    Electronic ISSN: 1944-7973
    Topics: Architecture, Civil Engineering, Surveying , Geography
    Published by Wiley on behalf of American Geophysical Union (AGU).
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  • 3
    Publication Date: 2011-03-09
    Description: It is often assumed that antibiotics act on the most vulnerable cellular targets, particularly those that require limited inhibition to block growth. To evaluate this assumption, we developed a genetic method that can inducibly deplete targeted proteins and that mimics their chemical inactivation. We applied this system to current antibiotic targets in mycobacteria. Although depleting some antibiotic targets significantly perturbs bacterial growth, surprisingly, we found that reducing the levels of other targets by more than 97% had little or no effect on growth. For one of these targets, dihydrofolate reductase, metabolic analysis suggested that depletion mimics the use of subinhibitory concentrations of the antibiotic trimethroprim. These observations indicate that some drug targets can exist at levels much higher than are needed to support growth. However, protein depletion can be used to identify promising drug targets that are particularly vulnerable to inhibition.
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 4
    Publication Date: 1991-04-26
    Description: The toluene extract of the fluffy carbon material produced by resistive heating of graphite contains a variety of molecules larger than C(60) and C(70) in a total amount of 3 to 4% by weight. Repeated chromatography of this material on neutral alumina has led to the isolation of stable solid samples of C(76), C(84), C(90), and C(94). The characterization, which includes mass spectrometry, (13)C nuclear magnetic resonance, electronic absorption (ultraviolet/visible) and vibrational (infrared) spectroscopy identifies these all-carbon molecules as higher fullerenes. In addition, C(70)O, a stable oxide, has been isolated that is structurally and electronically closely related to D5h-C(70). This compound forms during the resistive heating process and probably has an oxygen atom inserted between two carbon atoms on the convex external surface of the C(70) skeleton.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Diederich, F -- Ettl, R -- Rubin, Y -- Whetten, R L -- Beck, R -- Alvarez, M -- Anz, S -- Sensharma, D -- Wudl, F -- Khemani, K C -- Koch, A -- New York, N.Y. -- Science. 1991 Apr 26;252(5005):548-51.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17838488" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 1991-07-12
    Description: Atomic force microscopy and x-ray diffractometry were used to study 1500 A-thick films of pure C(60) grown by sublimation in ultrahigh vacuum onto a CaF(2) (111) substrate. Topographs of the films did not reveal the expected close-packed structures, but they showed instead large regions that correspond to a face-centered cubic (311) surface and distortions of this surface. The open (311) structure may have a relatively low free energy because the low packing density contributes to a high entropy of the exposed surface.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Snyder, E J -- Anderson, M S -- Tong, W M -- Williams, R S -- Anz, S J -- Alvarez, M M -- Rubin, Y -- Diederich, F N -- Whetten, R L -- New York, N.Y. -- Science. 1991 Jul 12;253(5016):171-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17779132" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 6
    Publication Date: 2016-05-03
    Print ISSN: 0043-1397
    Electronic ISSN: 1944-7973
    Topics: Architecture, Civil Engineering, Surveying , Geography
    Published by Wiley on behalf of American Geophysical Union (AGU).
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  • 7
    Publication Date: 1989-09-08
    Description: The unambiguous structural characterization of a single-sized all-carbon molecule requires its chemical synthesis. For cyclo[18]carbon, ab initio calculations predict a relatively stable, cyclic D9h ground state geometry with alternating C-C (1.36 angstroms) and C identical withC (1.20 angstroms) bonds. The synthesis and x-ray crystal structure of a direct precursor to C(18) are described. The analysis of laser flash heating experiments on this precursor by time-of-flight mass spectroscopy shows a sequence of retro-Diels-Alder reactions leading to C(18) as the predominant fragmentation pattern. Structural evidence is provided for the generation of an all-carbon molecule from a well-characterized organic precursor.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Diederich, F -- Rubin, Y -- Knobler, C B -- Whetten, R L -- Schriver, K E -- Houk, K N -- Li, Y -- New York, N.Y. -- Science. 1989 Sep 8;245(4922):1088-90.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17838807" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 8
    Publication Date: 2015-06-20
    Description: The efficiency of biological photosynthesis results from the exquisite organization of photoactive elements that promote rapid movement of charge carriers out of a critical recombination range. If synthetic organic photovoltaic materials could mimic this assembly, charge separation and collection could be markedly enhanced. We show that micelle-forming cationic semiconducting polymers can coassemble in water with cationic fullerene derivatives to create photoinduced electron-transfer cascades that lead to exceptionally long-lived polarons. The stability of the polarons depends on the organization of the polymer-fullerene assembly. Properly designed assemblies can produce separated polaronic charges that are stable for days or weeks in aqueous solution.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Huber, Rachel C -- Ferreira, Amy S -- Thompson, Robert -- Kilbride, Daniel -- Knutson, Nicholas S -- Devi, Lekshmi Sudha -- Toso, Daniel B -- Challa, J Reddy -- Zhou, Z Hong -- Rubin, Yves -- Schwartz, Benjamin J -- Tolbert, Sarah H -- 1S10RR23057/RR/NCRR NIH HHS/ -- P41GM103393/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2015 Jun 19;348(6241):1340-3. doi: 10.1126/science.aaa6850.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemistry and Biochemistry, University of California-Los Angeles (UCLA), Los Angeles, CA 90095-1569, USA. ; Department of Microbiology, Immunology and Molecular Genetics, and the Biomedical Engineering Program, UCLA, Los Angeles, CA 90095, USA. ; Department of Microbiology, Immunology and Molecular Genetics, and the Biomedical Engineering Program, UCLA, Los Angeles, CA 90095, USA. The California NanoSystems Institute (CNSI), UCLA, Los Angeles, CA 90095, USA. ; Department of Chemistry and Biochemistry, University of California-Los Angeles (UCLA), Los Angeles, CA 90095-1569, USA. tolbert@chem.ucla.edu schwartz@chem.ucla.edu rubin@chem.ucla.edu. ; Department of Chemistry and Biochemistry, University of California-Los Angeles (UCLA), Los Angeles, CA 90095-1569, USA. The California NanoSystems Institute (CNSI), UCLA, Los Angeles, CA 90095, USA. tolbert@chem.ucla.edu schwartz@chem.ucla.edu rubin@chem.ucla.edu. ; Department of Chemistry and Biochemistry, University of California-Los Angeles (UCLA), Los Angeles, CA 90095-1569, USA. The California NanoSystems Institute (CNSI), UCLA, Los Angeles, CA 90095, USA. Department of Materials Science and Engineering, UCLA, Los Angeles, CA 90095, USA. tolbert@chem.ucla.edu schwartz@chem.ucla.edu rubin@chem.ucla.edu.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/26089510" target="_blank"〉PubMed〈/a〉
    Keywords: Electron Transport ; Fullerenes/*chemistry ; *Photosynthesis ; Polymers/*chemistry ; Semiconductors
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 9
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 113 (1991), S. 1050-1051 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 113 (1991), S. 2780-2781 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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