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  • Articles  (265)
  • Chemistry  (265)
  • ASTROPHYSICS
  • STRUCTURAL MECHANICS
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  • 2020-2022  (24)
  • 1950-1954  (241)
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  • 1
    facet.materialart.
    Unknown
    In:  http://aquaticcommons.org/id/eprint/15087 | 403 | 2014-05-28 03:22:35 | 15087 | United States National Marine Fisheries Service
    Publication Date: 2021-07-02
    Description: The population structure of walleye pollock (Theragrachalcogramma) in the northeastern Pacific Ocean remains unknown. We examined elemental signatures in the otoliths of larval and juvenile pollock from locations in the BeringSea and Gulf of Alaska to determine if there were significant geographic variations in otolith compositionthat may be used as natural tags of population affinities. Otoliths were assayed by using both electron probemicroanalysis (EPMA) and laser ablation inductively coupled plasma mass spectrometry (ICP-MS). Elements measured at the nucleus of otoliths by EPMA and laser ablation ICP-MS differed significantly among locations. However, geographicgroupings identified by a multivariate statistical approach from EPMA and ICP-MS were dissimilar, indicating that the elements assayed by each technique were controlled by separate depositional processes within the endolymph. Elemental profiles across the pollock otoliths were generally consistent at distances up to 100 μm from the nucleus. At distances beyond 100 μm, profiles varied significantly but were remarkably consistent among individuals collected at each location. These data may indicate that larvae from various spawning locations are encountering water masses with differing physicochemicalproperties through their larval lives, and at approximately the same time. Although our results are promising, we require a better understanding of the mechanisms controlling otolith chemistry before it will be possibleto reconstruct dispersal pathways of larval pollock based on probe-based analyses of otolith geochemistry. Elemental signatures in otoliths of pollock may allow for the delineation of fine-scale population structure in pollock that has yet to be consistently revealed by using population genetic approaches.
    Keywords: Chemistry ; Fisheries
    Repository Name: AquaDocs
    Type: article , TRUE
    Format: application/pdf
    Format: application/pdf
    Format: 604-616
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 66 (1954), S. 586-589 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Abhängigkeit der Trennung von Ceriterden in Austauschersäulen vom komplexbildenden Elutionsmittel und von der Art der Austauscherkationen wird untersucht. Bei Amino-tetraessigsäuren steigt die Trennwirkung in der Reihenfolge: Äthylendiamin-tetraessigsäure, o-Cyclohexan-diamino-tetraessigsäure, ββ′-Diaminoäthyläther-tetraessigsäure und Äthylenglykol-bis-β-aminoäthyläther-tetraessigsäure. Dies wird bei konstantem PH-Wert auf die sinkende Komplexitätskonstante und deren Abstufung in der Seltenen Erden-Reihe sowie auf die für die einzelnen Komplexbildner differierende PH-Abhängigkeit zurückgeführt. Die besten Trenneffekte zeigt Äthylenglykol-bis-β-aminoäthyläther-tetraessigsäure bei PH 6,75. Der Nalcite HCR-Austauscher ergibt in der NH4-Form gegenüber der H-Form nicht nur einen sofortigen Durchbruch, sondern auch ein beachtliches Trennergebnis. Unterschiede in der Wirkung bei der Na-, K- und NH4-Form einerseits und der Ca-Form andererseits werden erklärt.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 65 (1953), S. 347-347 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 321-335 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Vulcanization with sulfur is ascribed to the formation of sulfur radicals which are believed to copolymerize with the rubber molecule double bonds. Hydrogen sulfide is proposed as necessary for chain initiation but when formed in sufficient amounts serves as a chain terminator. This is believed to lead to numerous self-limiting features including ceiling temperatures, post-vulcanization and delayed action effects. Initiation may result from the oxidation of H2S to sulfur radicals and termination to the formation of HS radicals.
    Additional Material: 2 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 409-423 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: When the acetate groups of polyvinyl acetate are removed and subsequently restored, the viscosity of the polymer is usually decreased. It is found that after such processing, vinyl acetate polymers prepared at a given temperature approach a maximum viscosity regardless of the viscosity of the original resins. This maximum is increased by lowering the temperature of polymerization and is different for other vinyl esters. The extent of degradation is negligible at low conversions. It is concluded that this phenomenon is characteristic of the monomer. The chemical bond responsible for the degradation has many of the properties of ester linkages. The resins degrade with both bases and acids although the latter catalyst sometimes requires the presence of water. They also degrade when heated in a solution of pyridine, acetic acid and acetic anhydride. The extent of degradation closely parallels the degree of hydrolysis. It is suggested that these ester linkages are formed during polymerization as a result of transfer with the carbon-hydrogen bonds of the acetate groups of both monomer and polymer. Evidence of another transfer reaction involving the vinyl group, but having no bearing on the degradation, is also advanced. If polyvinyl acetate is alcoholized with an acid catalyst, in the absence of water, the processed resin may have a higher viscosity than would be the case with an alkaline catalyst. How much higher is governed by the type of initiator used in the polymerization. This suggests that polymer molecules may be united under these conditions, but the nature of the reaction is obscure.
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 6 (1951), S. 691-698 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Employing a reproducible system for the emulsion polymerization of styrene it has been demonstrated that agitation (stirring or shaking) affects both the rate of polymerization and maximum average molecular weight of the polymer formed. Increasing the agitation increases the inhibition, decreases the polymerization rate, and lowers the average molecular weight of the polymer formed. Agitation affects both a peroxide and a persulfate catalyzed polymerization in a similar manner. Agitation effects have been observed in the presence of a redox system and in the presence of a chain modifier. Oxygen has been demonstrated to stop as well as inhibit the initiation of an emulsion polymerization.
    Additional Material: 5 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 14 (1954), S. 121-123 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 13 (1954), S. 189-191 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 12 (1954), S. 309-315 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The densities and water contents of large β-lactoglobulin crystals were determined as a function of relative humidity. When the specific volumes of the crystals (1/density) were plotted against their water contents, a straight line was obtained between 14 and 46% water. The extrapolation of this line by the graphical intercept method of Lewis and Randall gave a value of 0.772 for the specific volume of the protein and 0.983 for the specific volume of the water in the β-lactoglobulin crystal. Subtracting the specific volume of the protein in the crystal from the specific volume of the anhydrous protein (0.802-0.772) gave a value of 0.030 ml. for the contraction of one gram protein on becoming hydrated.A value of 0.021 ml. was calculated for the contraction of water per gram protein by the difference between the apparent specific volume of the protein in solution, assuming water to have a specific volume of 1.003, and the value of 0.772 for the specific volume of the protein in the crystal. There was good correlation between the value for contraction of water as calculated from the ionic groups of the protein and the observed contraction value.
    Additional Material: 2 Ill.
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  • 10
    facet.materialart.
    Unknown
    In:  http://aquaticcommons.org/id/eprint/15161 | 403 | 2014-05-29 07:19:00 | 15161 | United States National Marine Fisheries Service
    Publication Date: 2021-07-03
    Description: The use of strontium-to-calcium (Sr/Ca) ratios in otoliths is becoming a standard method to describe life history type and the chronology of migrations between freshwater and seawater habitats in teleosts (e.g. Kalish, 1990; Radtke et al., 1990; Secor, 1992; Rieman et al., 1994; Radtke, 1995; Limburg, 1995; Tzeng et al. 1997; Volk et al., 2000; Zimmerman, 2000; Zimmerman and Reeves, 2000, 2002). This method provides critical information concerning the relationship and ecology of species exhibiting phenotypic variation in migratory behavior (Kalish, 1990; Secor, 1999).Methods and procedures, however, vary among laboratories because a standard method or protocol for measurement ofSr in otoliths does not exist. In this note, we examine the variations in analytical conditions in an effort to increase precision of Sr/Ca measurements. From these findings we argue that precision can be maximized withhigher beam current (although there is specimen damage) than previously recommended by Gunn et al. (1992).
    Keywords: Chemistry ; Fisheries
    Repository Name: AquaDocs
    Type: article , TRUE
    Format: application/pdf
    Format: application/pdf
    Format: 712-718
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