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  • Chemistry  (3)
  • Oceanography  (2)
  • INGALA  (1)
  • 2020-2022  (3)
  • 1980-1984  (3)
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  • 1
    facet.materialart.
    Unbekannt
    In:  http://aquaticcommons.org/id/eprint/7439 | 704 | 2011-12-05 12:54:50 | 7439 | Fundacion Charles Darwin Foundation
    Publikationsdatum: 2021-07-02
    Beschreibung: New Faces and New Projects in a New CDRS Department. International Workshop: Feral Goat Eradication Program. Geologists to Invade Galápagos. GIS in Galápagos. The Isabela Project: Off and Running. A Pig-Free Santiago: Is it a Dream or on the Horizon? The Special Law for Galápagos.
    Schlagwort(e): Conservation ; Galápagos ; conservation ; Charles Darwin Research Station ; feral goats ; geology ; Geographic Information Systems ; Isla Isabela ; Isla Santiago ; pigs ; legislation ; INGALA
    Repository-Name: AquaDocs
    Materialart: article
    Format: application/pdf
    Format: application/pdf
    Format: 2-6
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
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    In:  http://aquaticcommons.org/id/eprint/14316 | 8 | 2014-01-27 21:48:30 | 14316
    Publikationsdatum: 2021-07-10
    Beschreibung: EXTRACT (SEE PDF FOR FULL ABSTRACT):The seasonal cycles of coastal wind stress, adjusted sea level height (ASL), shelf currents and water temperatures off the west coast of North America (35°N to 48°N) were estimated by fitting annual and semiannual harmonics to data from 1981-1983. Longer records of monthly ASL indicate that these two harmonics adequately represent the long-term monthly average seasonal cycle, and that the current measurement period is long enough to define the seasonal cycles, with relatively small errors in magnitude and phase.
    Schlagwort(e): Atmospheric Sciences ; Oceanography ; PACLIM
    Repository-Name: AquaDocs
    Materialart: conference_item
    Format: application/pdf
    Format: application/pdf
    Format: 23-24
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
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    In:  http://aquaticcommons.org/id/eprint/14318 | 8 | 2014-12-10 23:37:25 | 14318
    Publikationsdatum: 2021-07-10
    Beschreibung: Principal coordinates analysis and multiple regression analysis were used to determine the environmental factors associated with the decline in phytoplankton production during and after the 1977 drought for the San Francisco Bay-Delta Estuary. Physical, chemical and biological data were collected semimonthly or monthly during the spring-summer between 1973 and 1982 from 15 sampling sites located throughout the Bay-Delta. A decline in phytoplanktoncommunity diversity and density during the 1977 drought and subsequent years (1978 through 1981) was described using principal coordinates analysis. The best multiple regression which described the changes in phytoplankton community succession contained the variables water temperature, wind velocity and ortho-phosphateconcentration. Together these variables accounted for 61 percent of the variation in the phytoplankton community among years described by principal coordinates analysis. An increase in water temperature, wind velocity and ortho-phosphate concentration within the Bay-Delta, beginning in June 1976 and continuing through 1981, was demonstrated using weighted moving averages. From the strong association between phytoplankton community succession and climatic variables it was hypothesized that the decline in phytoplankton production during and after the 1977 drought was associated with climatic changes within the northeast Pacific.
    Schlagwort(e): Ecology ; Environment ; Limnology ; Oceanography ; PACLIM
    Repository-Name: AquaDocs
    Materialart: conference_item
    Format: application/pdf
    Format: application/pdf
    Format: 25-25
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 63 (1980), S. 2302-2311 
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: This paper deals with the problem of defining, and measuring, the pH inside the water pool (which we define as pHwp) of reverse micelles, i.e. micelles formed by surfactants dissolved in apolar solvents in the presence of minimal amounts of water. The conceptual and experimental difficulties are discussed, and it is argued that no absolute determination of pHwp is possible, mostly because water in the water pools of reverse micelles is a new solvent, for which no standardization of acidity is available. The problem can be approached only on the basis of an empirical acidity scale.An empirical acidity scale for water pools in reverse micelles of bis (2-ethyl-hexyl) sodium sulfosuccinate (AOT) in isooctane has been defined by measuring the 31P-chemical shifts of phosphate buffers. The chemical shifts in bulk water were compared to those found in reverse micelles under the assumption that the pK of phosphate ion is the same in the two systems. It was found that in most cases there was little difference (less than 0.4 pH units) between pHwp and the pH of the starting buffer in bulk water (which we define as pHst). However, this difference between pHwp and pHst may become much larger in certain cases.The difference (pHwp-pHst) is measured under a variety of conditions, and this permits the determination of an operational acidity in the micelle water pools as a function of the pHst with which the aqueous micelles are prepared. The significance of such data for interpreting the behaviour of enzymes confined in the micelles water pool is discussed. Based on the pHwp scale, the apparent pKa of phenol-red and 4-nitrophenol were determined in reverse micelles containing different buffers and different water content. The pKa values obtained were rather sensitive to changes of both these factors, which was taken to signify that organic dies have only a very limited applicability to measure the acidity of the water pools of reverse micelles.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 3713-3726 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Fourier transform infrared (FTIR) spectroscopy is used to determine the cure rate of an epoxy resin consisting of Tetraglycidyl-4,4′-diaminodiphenyl methane (TGDDM) and diaminodiphenylsulfone (DDS). Cure rates at 120 and 160°C are shown to increase noticeably when 1% BF3-MEA is added to either TGDDM to TGDDM plus DDS. Fluoroboric acid is shown to increase the cure rates even more than the BF3-MEA. These Results combined with the NMR results in the accompanying article indicate that BF3-MEA is not a catalyst for epoxy resin cure. Instead it is rapidly hydrolyzed to fluoroboric acid which acts as the catalyst.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 3697-3711 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Fluorine-19 NMR is used to examine the role of boron trifluoride monoethylamine (BF3-MEA) in epoxy resin cure. Spectra were first recorded in a variety of solvents suitable for dissolving different epoxy resins. All spectra contained a peak due to fluoroboric acid. Spectra of BF3-MEA in orthodichlorobenzene were then recorded at elevated temperatures. The floroboric acid peak area increased, indicating that the BF3-MEA was being hydrolyzed. Results indicate that, at temperatures above 100°C, BF3-MEA is completely hydrolyzed within 5 min to fluoroboric acid.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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