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The worldwide distribution of honeybees and their fast propagation to new areas rests on their ability to keep up optimal 'tropical conditions' in their brood nest both in the cold and in the heat. Honeybee colonies behave like 'superorganisms' where individuals work together to promote reproduction of the colony. Social cooperation has developed strongly in thermal homeostasis, which guarantees a fast and constant development of the brood. We here report on the cooperation of individuals in reaction to environmental variation to achieve thermal constancy of 34–36 °C. The measurement of body temperature together with bee density and in-hive microclimate showed that behaviours for hive heating or cooling are strongly interlaced and differ in their start values. When environmental temperature changes, heat production is adjusted both by regulation of bee density due to migration activity and by the degree of endothermy. Overheating of the brood is prevented by cooling with water droplets and increased fanning, which start already at moderate temperatures where heat production and bee density are still at an increased level. This interlaced change and onset of different thermoregulatory behaviours guarantees a graded adaptation of individual behaviour to stabilise the temperature of the brood. [ABSTRACT FROM AUTHOR]

Abstract: Vespine wasps are known for their high endothermic capacity. Endothermic activity is directly linked to respiration. However, knowledge on wasp respiration is sparse and almost nothing is known about their resting metabolism. We investigated the yellowjackets’ CO2 production in a flow-through respirometer chamber overnight. Endothermic and behavioral activity was observed by real-time infrared thermography. Most resting wasps were ectothermic or only slightly endothermic (thoracic temperature excess against abdomen <0.6°C). In the investigated temperature range (T a =2.9–42.4°C) mean CO2 production rate of resting wasps increased steeply according to an exponential function, from 5.658μlg−1 min−1 at 8.3°C to 8.504μlg−1 min−1 at 20.2°C, 58.686μlg−1 min−1 at 35.3°C and 102.84μlg−1 min−1 at 40°C. The wasps’ respiratory critical thermal maximum (CTmax), marking the upper edge of their viable temperature range, was 45.3°C. The respiratory CTmax did not differ significantly from the activity CTmax of 44.9°C. CTmax values were considerably below that of honeybees (48.9 and 49.0°C for respiration and activity, respectively). This allows honeybees to kill wasps by heat-balling. Comparison with other arthropods showed that vespine wasps are among the insects with the highest mass-specific resting metabolic rate and the steepest increase of metabolism with ambient temperature. [Copyright &y& Elsevier]

Abstract: Endothermic insects like honeybees and some wasps have to cope with an enormous heat loss during foraging because of their small body size in comparison to endotherms like mammals and birds. The enormous costs of thermoregulation call for optimisation. Honeybees and wasps differ in their critical thermal maximum, which enables the bees to kill the wasps by heat. We here demonstrate the benefits of a combined use of body temperature measurement with infrared thermography, and respiratory measurements of energy turnover (O2 consumption or CO2 production via flow-through respirometry) to answer questions of insect ecophysiological research, and we describe calibrations to receive accurate results. To assess the question of what foraging honeybees optimise, their body temperature was compared with their energy turnover. Honeybees foraging from an artificial flower with unlimited sucrose flow increased body surface temperature and energy turnover with profitability of foraging (sucrose content of the food; 0.5 or 1.5mol/L). Costs of thermoregulation, however, were rather independent of ambient temperature (13–30°C). External heat gain by solar radiation was used to increase body temperature. This optimised foraging energetics by increasing suction speed. In determinations of insect respiratory critical thermal limits, the combined use of respiratory measurements and thermography made possible a more conclusive interpretation of respiratory traces. [Copyright &y& Elsevier]

Abstract: A comparison of the thermoregulation of water foraging wasps (Vespula vulgaris, Polistes dominulus) under special consideration of ambient temperature and solar radiation was conducted. The body surface temperature of living and dead wasps was measured by infrared thermography under natural conditions in their environment without disturbing the insects’ behaviour. The body temperature of both of them was positively correlated with T a and solar radiation. At moderate T a (22–28°C) the regression lines revealed mean thorax temperatures (T th) of 35.5–37.5°C in Vespula, and of 28.6–33.7°C in Polistes. At high T a (30–39°C) T th was 37.2–40.6°C in Vespula and 37.0–40.8°C in Polistes. The thorax temperature excess (T th–T a) increased at moderate T a by 1.9°C (Vespula) and 4.4°C (Polistes) per kW−1 m−2. At high T a it increased by 4.0°C per kW−1 m−2 in both wasps. A comparison of the living water foraging Vespula and Polistes with dead wasps revealed a great difference in their thermoregulatory behaviour. At moderate T a (22–28°C) Vespula exhibited distinct endothermy in contrast to Polistes, which showed only a weak endothermic activity. At high T a (30–39°C) Vespula reduced their active heat production, and Polistes were always ectothermic. Both species exhibited an increasing cooling effort with increasing insolation and ambient temperature. [Copyright &y& Elsevier]

Abstract: The relation between the respiratory activity of resting honeybees and ambient temperature (T a) was investigated in the range of 5–40°C. Bees were kept in a temperature controlled flow through respirometer chamber where their locomotor and endothermic activity, as well as abdominal ventilatory movements was recorded by infrared thermography. Surprisingly, true resting bees were often weakly endothermic (thorax surface up to 2.8°C warmer than abdomen) at a T a of 14–30°C. Above 33°C many bees cooled their body via evaporation from their mouthparts. A novel mathematical model allows description of the relationship of resting (standard) metabolic rate and temperature across the entire functional temperature range of bees. In chill coma (<11°C) bees were ectothermic and CO2 release was mostly continuous. CO2 release rate (nls−1) decreased from 9.3 at 9.7°C to 5.4 at 5°C. At a T a of >11°C CO2 was released discontinuously. In the bees’ active temperature range mean CO2 production rate (nls−1) increased sigmoidally (10.6 at 14.1°C, 24.1 at 26.5°C, and 55.2 at 38.1°C), coming to a halt towards the upper lethal temperature. This was primarily accomplished by an exponential increase in gas exchange frequency (0.54 and 3.1breathsmin−1 at 14.1 and 38.1°C) but not in released CO2 volume per respiratory cycle (1487 and 1083nlcycle−1 at 14.1 and 38.1°C). Emission of CO2 bursts was mostly (98%) accompanied by abdominal ventilation movements even in small CO2 bursts. Larger bursts coincided with a longer duration of active ventilation. An increased amount of CO2 expelled per unit time of ventilation indicates a higher efficiency of ventilation at high ambient temperatures. [Copyright &y& Elsevier]

In honeybee colonies, guards protect their nest from various robbers including bees from other colonies. Infrared thermography showed that the guards and the bees examined by them (examinees) differ considerably in their thermal behaviour according to their particular role in the nestmate recognition process. The thorax surface temperature was on average higher and more variable in the examinees (36.1°C, S.D. = 4.14, N = 1545, 303 bees) than in the guards (34.0°C, s.n. = 2.00, N = 1681, 772 bees). During thorough examinations lasting longer than 30s, more than 60% of the examinees showed phases of intense thoracic heating of more than 2°C (maximum temperature 48.5°C), whereas most guards cooled down. Our data suggest that these examinees heat up their surface to enhance chemical signalling during examinations. [ABSTRACT FROM AUTHOR]

We measured the energy turnover (oxygen consumption) of honeybees (Apis mellifera carnica), which were free to move within Warburg vessels. Oxygen consumption of active bees varied widely depending on ambient temperature and level of activity, but did not differ between foragers (>18 d) and middle-aged hive bees (7–10 d). In highly active bees, which were in an endothermic state ready for flight, it decreased almost linearly, from a maximum of 131.4 μl O2 min−1 at 15 °C ambient temperature to 81.1 μl min−1 at 25 °C, and reached a minimum of 29.9 μl min−1 at 40 °C. In bees with low activity, it decreased from 89.3 μl O2 min−1 at 15 °C to 47.9 μl min−1 at 25 °C and 14.7 μl min−1 at 40 °C. Thermographic measurements of body temperature showed that with increasing activity, the bees invested more energy to regulate the thorax temperature at increasingly higher levels (38.8–41.2 °C in highly active bees) and were more accurate.Resting metabolism was determined in young bees of 1–7 h age, which are not yet capable of endothermic heat production with their flight muscles. Their energy turnover increased from 0.21 μl O2 min−1 at 10 °C to 0.38 μl min−1 at 15 °C, 1.12 μl min−1 at 25 °C, and 3.03 μl min−1 at 40 °C. At 15, 25 and 40 °C, this was 343, 73 and 10 times below the values of the highly active bees, respectively. The Q10 value of the resting bees, however, was not constant but varied in a U-shaped manner with ambient temperature. It decreased from 4.24 in the temperature range 11–21 °C to 1.35 in the range 21–31 °C, and increased again to 2.49 in the range 30–40 °C. We conclude that attempts to describe the temperature dependence of the resting metabolism of honeybees by Q10 values can lead to considerable errors if the measurements are performed at only two temperatures. An acceptable approximation can be derived by calculation of an interpolated Q10 according to the exponential function VO2=0.151×1.0784Ta (interpolated Q10=2.12). [Copyright &y& Elsevier]