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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 88 (1974), S. 129-140 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. Queens regulate thoracic temperature at 35–38 °C, and abdominal temperature at 31–36 °C while incubating their brood at ambient temperatures from 3 ° to 33 °C (Fig. 1). 2. The queen's brood clump, containing poikilothermic eggs, larvae and pupae, is incubated for long durations both during the day and at night (Figs. 2 and 3). 3. Brood temperature is maintained relatively independent from ambient temperature, but it does not appear to be maintained at specific temperature set-points. The difference between brood and ambient temperature during incubation is nearly 20 °C at an ambient temperature of 5 °C, and only 3 °C at 30 °C (Fig. 4). 4. The rate of oxygen consumption of incubating queens increases linearly with decreasing ambient temperatures (Fig. 6), and the temperature difference between the incubating queen and her brood is directly related to her rate of oxygen consumption (Fig. 7). 5. The “regulation” of brood temperature is explicable in terms of the regulation of abdominal temperature. The results are discussed with regard to vertebrate homeotherms, and with respect to energetics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 78 (1972), S. 337-345 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Muscle potentials were recorded extracellularly from the fibrillar flight muscles ofBombus sonorus andB. fervidus during shivering and during flight. During some bouts of shivering motor units of the same muscles, of synergistic muscles, and of antagonistic muscles were excited with relatively synchronous bursts of impulses. These bursts were separated from each other by varying intervals. The latency between the beginning of bursts in different units of antagonistic muscles was usually less than 12 msec. However, during other bouts of less vigorous shivering the synchrony was less precise. During any one portion of flight the interspike intervals of any one muscle unit were relatively constant, and all possible phase relationships were observed between the different muscles. The results show that control of fibrillar muscle involves 1) the average frequency of activation of individual muscles and 2) timing of the activation of muscles with respect to each other.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 82 (1973), S. 195-206 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. The rate of increase in thoracic temperature was strongly dependent on ambient temperature during pre-flight -warm-up in the sphinx moths,Hyles euphorbia andDeilephila elpenor (Figs. 1, 2). 2. The duration of pre-flight warm-up at 19–21 ° C was not correlated with mean body weight (0.3–3.5 g) in 13 species of sphinx moths (Kg. 3). 3. The mean rates of oxygen consumption during uninterrupted free flight forH. euphorbia andD. elpenor were 55 and 60 ml O2/g/hr respectively, regardless of air temperature at 15 and 22 ° C (Table 1, Fig. 4). 4. Thoracic temperature of sphinx moths of 13 species in free flight in the field usually ranged from 38 to 43 ° C, being independent of mean body weight (Fig. 5) but strongly correlated with weight-relative wing area (Fig. 6). 5. These data, which give no indication of regulation of heat production during warm-up or during flight, are in marked contrast with numerous previous publications on endothermy in moths.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bradford : Emerald
    Business process management journal 11 (2005), S. 709-723 
    ISSN: 1355-2503
    Source: Emerald Fulltext Archive Database 1994-2005
    Topics: Economics
    Notes: Purpose - The purpose of this paper is to address two questions: what is the difference between relationship processes and purely product-oriented processes? And to answer this question we should bear in mind what we mean by relationship, and why a customer is willing to establish and maintain a relationship at all. Design/methodology/approach - An empirical analysis subjected the motives of customers and factors for the establishment and expansion of customers' relationships. In this context the relationship motives and factors can act as base to derive strategic goals of CRM and relationship processes in a further step. Findings - Based on strategic relationship goals the paper will give answers to a systematic identification and engineering of relationship activities and processes. Thereby relationship-oriented activities complement present product-oriented processes. In contrast to this we derive purely relationship-oriented processes as well, such as the customer recovery process. Such processes do not target product sales any more than rather the sustainability of relationship (in particular to valuable customers). Originality/value - The benefit of the paper is an integrated and goal-oriented derivation and design of relationship processes and activities. An example in financial services illustrates the approach and shows its application in parts.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 134 (1979), S. 113-117 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The bumblebees,Bombus edwardsii, move upward while visiting consecutive flowers on artificial “inflorescences”. This response is unrelated to the vertical patterning of rewards in the flowers of inflorescences. However, when rewards are greatest in the bottommost flowers the bees learn to start lower and leave before reaching the topmost (empty) flowers. Conversely, when rewards are greatest in the topmost flowers they tend to start in the middle of the inflorescence and depart from the top. When rewards are equal in all flowers bees start near the bottom and depart near the top of inflorescences. These behavioral patterns tend to maximize the number of visits to rewarding flowers while minimizing visits to non-rewarding flowers, thereby enhancing foraging returns.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 239 (1972), S. 223-225 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Bombus vosnesenskii Radowskowski queens were obtained near Berkeley, California, in January while they were foraging from manzanita (Arctostaphylos sp.). The bees were maintained in the laboratory where they were provided with ample sucrose solution. The queens utilized pollen clumps (on the floor ...
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 77 (1972), S. 49-64 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Temperature regulation inBombus terricola was investigated in the field in relation to foraging energetics on flowers differing widely in morphology and nectar contents. 1. While foraging for nectar fromAsclepias syriaca mean thoracic temperature (TTh) was relatively independent from ambient thermal conditions, ranging from 35.2 °C in shade at 12 °C, to 37.5 °C in sunshine at 28 °C (Fig. 1). 2. While foraging for pollen fromSolanum dulcamara TTh was also regulated near 36 °C (Fig. 2). 3. In contrast, mean TTh ofB. terricola foraging fromSpiraea latifolia andSolidago canadensis varied nearly directly with ambient thermal conditions (Figs. 4 and 5). 4. Abdominal temperature varied nearly directly with TA regardless of whether or not TTh was stabilized (Figs. 1 and 4). 5. At TA〈21 °C in shade many of the nectar foragers onSolidago canadensis andSpiraea latifolia, having a TTh 〈 29 °C, were incapable of immediate flight. However, the TTh of pollen gatherers at the same TA (Table 1) was higher (p 〈 0.01), and these bees were always capable of immediate flight. 6. The energetic costs for temperature regulation during foraging at different TA, and the energetic gains that might be derived are discussed (see Figs. 7 and 8) in relation to the geometry of nectar distribution in space, and in relation to nectar abundance.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 77 (1972), S. 65-79 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. The thoracic temperatures (TTh) of captiveBombus edwardsii queens and drones from the current year approached ambient temperatures (TA) at night, but warm-up was frequent throughout the day. 2. ABombus vosnesenskii queen which had initiated nest building maintained TTh nearly continuously between 37.4 and 38.8 °C at night and in the daytime. On the other hand, the TTh of an overwintered queen which was not “broody” was close to TA (about 22 °C), except when the bee walked from the nest box and fed on sugar syrup, when TTh approached 40 °C. 3. Workers and queens applied themselves closely to cocoons and heated them by body contact. The temperature of the cocoons declined when the attending workers depleted the honey in the nest. 4. Bees achieved a large difference between TTh and TA while being stationary when no wing movements were visible. Thoracic temperature subsequently declined when they were made to fly in place while suspended from the thread-like thermocouple leads. 5. Workers ofB. edwardsii maintained a mean TTh of 37.3 °C while foraging for nectar fromArctostaphylos otayensis at dawn when there was frost on the ground and TA near the flowers was 2 to 3 °C.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Oecologia 40 (1979), S. 235-245 
    ISSN: 1432-1939
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Differences in the foraging behavior of B. terricola workers on white clover, Trifolium repens, were examined on previously unvisited (filled) and depleted flowers, and as a function of flower-head density. 1. The number of florets visited per unit time was independent of flower head density from 20 to at least 290 heads/m2, in part because the bees utilized more florets per head at low flower head densities, and also because they approached but rejected more flower heads at high rather than at low flower head densities. 2. Previously visited clover-heads were approached but often rejected, while unvisited heads were not rejected. 3. The bees behaved markedly different while foraging in patches of flowers which were available to all foragers, than in those which had been screened and contained on the average 3.9 times more sugar; they tendent to move through depleted areas and to concentrate in rich areas. On successive flower-head visits in depleted areas they moved more forward than backward (82% vs. 18%), while in rich areas they tended to move almost as much backward as forward 47% vs. 53%). 4. The distances of inter-head moves were approximately twice as long in depleted as in rich areas. 5. The bees visited almost as many florets per unit time in the rich as in the depleted areas (32 vs. 35 per min). But in the rich patches they probed on the average into 11.6 florets per head in contrast to only 2.3 florets per depleted head. 6. In an experiment with B. vagans workers foraging from Aconitum napellus inflorescences, the bees did not reject previously visited flowers, and they moved upward in successive flower visits on inverted as well as on unaltered inflorescences. On horizontal inflorescences they moved both right and left. The movements are not a direct response to nectar differences, nor to differences in average nectar distributions. The systematic foraging behavior on vertical inflorescences may thus be a mechanism of reducing the revisiting of just-emptied flowers.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Oecologia 42 (1979), S. 325-337 
    ISSN: 1432-1939
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary An analysis of the foraging behaviors of several species of palatable and unpalatable lepidopterous larvae indicates that palatable caterpillars partition their time between feeding and behaviors that could be related to escape visually oriented predators. Depending on the species, palatable caterpillars do all or several of the following: 1) restrict themselves to the underside of leaves at all times, 2) restrict foraging to night-time, 3) commute to and from their feeding area on leaves, 4) move from the unfinished leaf to a distant leaf after a feeding bout, thus removing themselves from the evidence of their eating, 5) snip off partially-eaten leaves after feeding on them. The less palatable, or unpalatable, caterpillars do not snip off partially-eaten leaves, feed from leaves leaving tattered edges, and are often exposed resting and feeding on the leaf surfaces in direct sunshine. I conclude that some caterpillar foraging behaviors may have evolved under the selective pressure of visually-oriented predators that use leaf-damage as a cue in their searching behavior.
    Type of Medium: Electronic Resource
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