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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]

Simple Summary: Ambient temperature is a main external parameter in the life of ectothermic insects. It affects egg and larval development as well as adults' survival, thriving and propagation, and successful overwintering. We conducted temperature measurements in Central Europe in the habitat and in the microhabitats of Pyrrhocoris apterus, a herbivorous bug species almost ubiquitous in Eurasia, with a high invasive potential (USA, Central America, India and Australia). and set them against freely available climate data commonly used to characterize habitat climate. Our temperature measurements were also compared to the bug species' thermal limits (critical thermal minima and maxima). Ambient temperatures outside the thermal boundaries of P. apterus can and do occur in the habitat. Microhabitat measurement showed that in summer, individuals simply moved from hot areas to cooler ones, and in winter they sought areas with bearable temperatures for hibernation. Temperatures in these particular areas are not (always) represented in large-scale climate tables, leading to possible misinterpretation of the future dispersal behavior, e.g., of invasive species. Ambient temperature is a main parameter that determines the thriving and propagation of ectothermic insects. It affects egg and larval development as well as adults' survival and successful overwintering. Pyrrhocoris apterus is a herbivorous bug species almost ubiquitous in Eurasia. Its distribution extends from the Atlantic Coast to Siberia, Northwest China and Mongolia. After introduction, it established successfully in the USA, Central America, India and Australia, which indicates a high invasive potential of this species. We determined the climatic conditions in Central Europe in a habitat where P. apterus has been continuously observed for decades. We conducted temperature measurements in the habitat and in the microhabitats where individuals could be found during the year and set them against freely available climate data commonly used to characterize habitat climate. Our temperature measurements were also compared to thermal limits (critical thermal minima and maxima). Although ambient temperatures outside the thermal boundaries of P. apterus can and do occur in the habitat, the bugs thrive and propagate. Microhabitat measurement in winter showed that individuals sought areas with favorable temperatures for hibernation. In particular, these areas are not (always) represented in large-scale climate tables, leading to possible misinterpretation of future patterns of spread of invasive species spread. [ABSTRACT FROM AUTHOR]

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: 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]

The CO2 production of individual larvae ofApis mellifera carnica, which were incubated within their cells at a natural air humidity of 60-80%, was determined by an open-flow gas analyzer in relation to larval age and ambient temperature. In larvae incubated at 34 °C the amount of CO2 produced appeared to fall only moderately from 3.89±1.57 µl mg-1 h-1 in 0.5-day-old larvae to 2.98±0.57 µl mg-1 h-1 in 3.5-day-old larvae. The decline was steeper up to an age of 5.5 days (0.95±1.15 µl mg-1 h-1). Our measurements show that the respiration and energy turnover of larvae younger than about 80 h is considerably lower (up to 35%) than expected from extrapolations of data determined in older larvae. The temperature dependency of CO2 production was determined in 3.5-day-old larvae, which were incubated at temperatures varying from 18 to 38 °C in steps of 4 °C. The larvae generated 0.48±0.03 µl mg-1 h-1 CO2 at 18 °C, and 3.97±0.50 µl mg-1 h-1 CO2 at 38 °C. The temperature-dependent respiration rate was fitted to a logistic curve. We found that the inflection point of this curve (32.5 °C) is below the normal brood nest temperature (33-36 °C). The averageQ10 was 3.13, which is higher than in freshly emerged resting honeybees but similar to adult bees. This strong temperature dependency enables the bees to speed up brood development by achieving high temperatures. On the other hand, the results suggest that the strong temperature dependency forces the bees to maintain thermal homeostasis of the brood nest to avoid delayed brood development during periods of low temperature. [ABSTRACT FROM AUTHOR]

The metabolism of ectotherms is temperature-dependent, and the exponential nature of the metabolic rate- temperature relationship means that warmer temperatures are disproportionately affecting the energy balance. T SB a sb (standard met.) temperature deviation from microclimate ambient nest temperature was -3.6 °C in I P. dominula i , -2.4 °C in I P. gallicus i , and -3.3 °C in I P. biglumis i ). The energetic calculations were conducted using temperature-dependent metabolic rate models of the three I Polistes i species, I P. dominula i , I P. gallicus i and I P. biglumis i [[17], [29]], and adequate body temperature models [[4], [17]]. The nest ambient air temperatures in the three habitats were clearly elevated above the meteorological standard ambient temperature recorded by the nearest weather stations (temperature difference, I P. dominula i : 3.6 °C, I P. gallicus i : 2.4 °C, I P. biglumis i : 3.3 °C; Figure 2). [Extracted from the article]

Winter in climatic regions with low temperatures is a challenge for overwintering insects. They are exposed to temperature extremes, which directly cause mortality or lead to energy depletion. The winter hibernaculum of paper wasp gynes protects from predators and rain, but only poorly from ambient temperature. In order to detect physiological adaptations to differing climates, we compared the respiratory metabolism of overwintering gynes of two polistine species from the Mediterranean climate in Italy (Polistes dominula and Polistes gallicus), and of one species from the temperate climate in Austria (Polistes dominula). The wasps' CO2 emission was measured with stop‐flow respirometry in a temperature range from 2.5 to 20 °C. The mass‐specific standard (resting) metabolic rate, the main type of metabolism of the dormant insects during overwintering, increased exponentially with ambient temperature but was suppressed in comparison to individuals measured in the summer, which conserves the energy stores. In addition, it was lower in the Mediterranean species (P. dominula and P. gallicus) in comparison to the temperate species (P. dominula), especially at higher temperatures. The active metabolic rate was suppressed to a similar amount. The suppressed metabolism of the overwintering Mediterranean gynes could be an adaptation to the higher winter temperatures to prevent a premature depletion of the energy resources. [ABSTRACT FROM AUTHOR]

We investigated the respiration patterns of wasps (Vespula sp.) in their viable temperature range (2.9–42.4°C) by measuring CO2 production and locomotor and endothermic activity. Wasps showed cycles of an interburst–burst type at low ambient temperatures (T a <5°C) or typical discontinuous gas exchange patterns with closed, flutter and open phases. At high T a of >31°C, CO2 emission became cyclic. With rising T a they enhanced CO2-emission primarily by an exponential increase in respiration frequency, from 2.6mHz at 4.7°C to 74mHz at 39.7°C. In the same range of T a CO2 release per cycle decreased from 38.9 to 26.4μlg−1 cycle−1. A comparison of wasps with other insects showed that they are among the insects with a low respiratory frequency at a given resting metabolic rate (RMR), and a relatively flat increase of respiratory frequency with RMR. CO2 emission was always accompanied by abdominal respiration movements in all open phases and in 71.4% of the flutter phases, often accompanied by body movements. Results suggest that resting wasps gain their highly efficient gas exchange to a considerable extent via the length and type of respiration movements. [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]

Climate change is expected to produce shifts in species distributions as well as behavioural and physiological adaptations to find suitable conditions or to cope with the altered environment. The paper wasps Polistes dominula and Polistes gallicus are closely related species, native in the European Mediterranean region and North Africa. P. dominula has expanded its range to the relatively cooler climates of Northern and Eastern Europe, but P. gallicus remained in its original distribution area. In order to reveal their metabolic adaptation to the current climate conditions, and the impact on energy demand at future climate conditions, we investigated the respiratory metabolic rate (CO 2 production) of P. dominula from Austria and P. gallicus from Italy. In contrast to the metabolic cold adaptation hypothesis their standard metabolic rate was nearly the same and increased in a typical exponential course with increasing ambient temperature. The metabolic rate of active wasps was higher than the standard metabolic rate and increased with the wasps' activity. There was no obvious difference in the active metabolism between the two species, with the exception that some P. gallicus individuals showed some extraordinary high values. A simultaneous measurement of metabolic rate and body temperature revealed that increased CO 2 production was accompanied by endothermic activity. The two investigated populations of paper wasps are quite similar in their metabolic response to temperature, although they live in different climate regions. The spread of P. dominula into cooler regions did not have significant influence on their active and standard metabolic rate. Unlabelled Image • A comparison of the standard and active metabolic rate of Polistes dominula and P. gallicus from different climates revealed similarities. • The metabolic rate was nearly the same in both species. • Simultaneous measurement of metabolism and body temperature revealed that increased CO 2 production is accompanied by endothermic activity. [ABSTRACT FROM AUTHOR]

Heteroptera, or true bugs populate many climate zones, coping with different environmental conditions. The aim of this study was the evaluation of their thermal limits and derived traits, as well as climatological parameters which might influence their distribution. We assessed the thermal limits (critical thermal maxima, CTmax, and minima, CTmin) of eight seed bug species (Lygaeidae, Pyrrhocoridae) distributed over four Köppen–Geiger climate classification types (KCC), approximately 6° of latitude, and four European countries (Austria, Italy, Croatia, Bulgaria). In test tubes, a temperature ramp was driven down to −5 °C for CTmin and up to 50 °C for CTmax (0.25 °C/min) until the bugs' voluntary, coordinated movement stopped. In contrast to CTmin, CTmax depended significantly on KCC, species, and body mass. CTmax showed high correlation with bioclimatic parameters such as annual mean temperature and mean maximum temperature of warmest month (BIO5), as well as three parameters representing temperature variability. CTmin correlated with mean annual temperature, mean minimum temperature of coldest month (BIO6), and two parameters representing variability. Although the derived trait cold tolerance (TC = BIO6 − CTmin) depended on several bioclimatic variables, heat tolerance (TH = CTmax − BIO5) showed no correlation. Seed bugs seem to have potential for further range shifts in the face of global warming. [ABSTRACT FROM AUTHOR]