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  • 1
    ISSN: 1437-9546
    Keywords: Key words  Vigilance ; Group size ; Gender ; Foraging ; Antipredator
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract   Vigilance in vertebrates is often inversely related to group size. We present evidence that distance to bushes and location within the herd are also critical factors in vigilance in springbok (Antidorcas marsupialis) in Etosha National Park, Namibia, where they are the preferred prey of cheetahs (Acinonyx jubatus). Most springbok feed in heterospecific herds, both by grazing on grass and browsing on bushes. We studied 1245 animals; variations in vigilance (time alert) were explained by location within the herd, distance to bushes and roads, number of springbok in each herd, and gender and age. Vigilance time decreased with increasing herd size, with increasing distance to bushes and roads, and with density. Springbok on the edge of herds devoted significantly more time to vigilance than did those in other locations, and vigilance in edge animals decreased with group size. Adults were more vigilant than young, and males were more vigilant than females. Position within the herd, and distance from bushes, were the most important variables influencing vigilance. Location in the herd and gender/age affected both browsing and grazing springbok, although other factors accounted for the differences in vigilance between browsing and grazing springbok: 1) group size was not significant for browsers, but it was for grazers, and 2) distances to bushes and road were not significant for browsers, but they were for grazers. These data relate to the risk from predators and the benefits from other group members. Springbok in bushes cannot see all members of the herd, cannot derive early warning from many group members, and are more at risk from predators because the latter can hide in the bushes.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 4 (1981), S. 218-223 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Column preparation ; “Split” vs. “on-column” injection ; Amino acid analysis, quantitative 10 ng level ; Average relative standard deviation 1% ; Fish muscle protein analysis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A carefully Standardized technique is described for the preparation of glass capillary columns which can be used successfully for routine quantitative amino acid analysis. Comparison is made between two different modes of sample injection. Preliminary quantitative results from “split” injection and “on-column” injection techniques are evaluated statistically and it is concluded that the “on-column” system is a prerequisite for quantitative amino acid analysis by glass capillary gas chromatography. An analysis of fish muscle protein hydrolyzate illustrates an application of this technique and results are compared with those from a packed column analysis.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 9 (1986), S. 555-560 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, fused-silica ; Plasma amino acid analysis ; “On-column” injection ; Classical ion exchange ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A capillary chromatographic procedure using a fused silica column is described which can be used to quantitatively determine amino acids in plasma following the pre-chromatographic “clean-up” described in a recent paper [1]. In substituting this procedure for that involving a packed column, advantage has been taken of the greater resolving power to separate amino acids from background component peaks. In order to extend this advantage and provide a sound basis for quantitative analysis, the technique of cold on-column injection was employed. As a result, good precision of standard analysis was obtained with relative standard deviation (RSD) values for all amino acids of less than 4%. Application of the entire procedure to plasma samples yields RSD values of better than 10% for all amino acids with recoveries ranging from 72% to 104%. Simultaneous determination of plasma amino acid levels by gas chromatography (GC) using capillary columns and by classical ion exchange (CIE) showed reasonable agreement. Statistical evaluation showed no significant difference between twelve amino acids. Values for the remaining two, namely, phenylalanine and histidine are significantly different (p 〈 0.005). Comparison of the values obtained from GC capillary and packed columns reveals no significant difference between fourteen amino acids. Significant differences exist between results for phenylalanine and tyrosine (p 〈 0.001). It is concluded that there is good agreement between data obtained by GC capillary and CIE techniques and that differences between results for phenylalanine and histidine are method related.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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