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      Honeybee Colony Thermoregulation – Regulatory Mechanisms and Contribution of Individuals in Dependence on Age, Location and Thermal Stress

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          Abstract

          Honeybee larvae and pupae are extremely stenothermic, i.e. they strongly depend on accurate regulation of brood nest temperature for proper development (33–36°C). Here we study the mechanisms of social thermoregulation of honeybee colonies under changing environmental temperatures concerning the contribution of individuals to colony temperature homeostasis. Beside migration activity within the nest, the main active process is “endothermy on demand” of adults. An increase of cold stress (cooling of the colony) increases the intensity of heat production with thoracic flight muscles and the number of endothermic individuals, especially in the brood nest. As endothermy means hard work for bees, this eases much burden of nestmates which can stay ectothermic. Concerning the active reaction to cold stress by endothermy, age polyethism is reduced to only two physiologically predetermined task divisions, 0 to ∼2 days and older. Endothermic heat production is the job of bees older than about two days. They are all similarly engaged in active heat production both in intensity and frequency. Their active heat production has an important reinforcement effect on passive heat production of the many ectothermic bees and of the brood. Ectothermy is most frequent in young bees (<∼2 days) both outside and inside of brood nest cells. We suggest young bees visit warm brood nest cells not only to clean them but also to speed up flight muscle development for proper endothermy and foraging later in their life. Young bees inside brood nest cells mostly receive heat from the surrounding cell wall during cold stress, whereas older bees predominantly transfer heat from the thorax to the cell wall. Endothermic bees regulate brood comb temperature more accurately than local air temperature. They apply the heat as close to the brood as possible: workers heating cells from within have a higher probability of endothermy than those on the comb surface. The findings show that thermal homeostasis of honeybee colonies is achieved by a combination of active and passive processes. The differential individual endothermic and behavioral reactions sum up to an integrated action of the honeybee colony as a superorganism.

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          Behavioral performance in adult honey bees is influenced by the temperature experienced during their pupal development.

          To investigate the possible consequences of brood-temperature regulation in honey bee colonies on the quality of behavioral performance of adults, we placed honey bee pupae in incubators and allowed them to develop at temperatures held constant at 32 degrees C, 34.5 degrees C, and 36 degrees C. This temperature range occurs naturally within hives. On emergence, the young adult bees were marked and introduced into foster colonies housed in normal and observation hives and allowed to live out their lives. No obvious difference in within-hive behavior was noted between the temperature-treated bees and the foster-colony bees. However, when the temperature-treated bees became foragers and were trained to visit a feeder 200 m from the hive, they exhibited clear differences in dance performance that could be correlated with the temperatures at which they had been raised: bees raised at 32 degrees C completed only approximately 20% of the dance circuits when compared with bees of the higher-temperature group. Also, the variance in the duration of the waggle phase is larger in 32 degrees C-raised bees compared with 36 degrees C-raised bees. All other parameters compared across all groups were not significantly different. One-trial learning and memory consolidation in the bees raised at different temperatures was investigated 1 and 10 min after conditioning the proboscis-extension reflex. Bees raised at 36 degrees C performed as expected for bees typically classified as "good learners," whereas bees raised at 32 degrees C and 34.5 degrees C performed significantly less well. We propose that the temperature at which pupae are raised will influence their behavioral performance as adults and may determine the tasks they carry out best inside and outside the hive.
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            Synaptic organization in the adult honey bee brain is influenced by brood-temperature control during pupal development.

            Recent studies have shown that the behavioral performance of adult honey bees is influenced by the temperature experienced during pupal development. Here we explore whether there are temperature-mediated effects on the brain. We raised pupae at different constant temperatures between 29 and 37 degrees C and performed neuroanatomical analyses of the adult brains. Analyses focused on sensory-input regions in the mushroom bodies, brain areas associated with higher-order processing such as learning and memory. Distinct synaptic complexes [microglomeruli (MG)] within the mushroom body calyces were visualized by using fluorophore-conjugated phalloidin and an antibody to synapsin. The numbers of MG were different in bees that had been raised at different temperatures, and these differences persisted after the first week of adult life. In the olfactory-input region (lip), MG numbers were highest in bees raised at the temperature normally maintained in brood cells (34.5 degrees C) and significantly decreased in bees raised at 1 degrees C below and above this norm. Interestingly, in the neighboring visual-input region (collar), MG numbers were less affected by temperature. We conclude that thermoregulatory control of brood rearing can generate area- and modality-specific effects on synaptic neuropils in the adult brain. We propose that resulting differences in the synaptic circuitry may affect neuronal plasticity and may underlie temperature-mediated effects on multimodal communication and learning.
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              Hot bees in empty broodnest cells: heating from within.

              Honeybee colonies maintain brood nest temperatures of 33-36 degrees C. We investigated brood nest thermoregulation at the level of individual worker behaviour and the transfer of heat from workers to the brood. Worker bees contribute to the regulation of brood nest temperature by producing heat while sitting motionless on the caps of brood cells. We report here an additional, newly observed heating strategy where heating bees enter empty cells between sealed brood cells and remain there motionless for periods of up to 45 min. Individually marked worker bees on the surface of sealed brood cells maintained thorax temperatures (T(th)) between 32.2+/-1.0 degrees C and 38.1+/-2.5 degrees C (mean +/- S.D.; N=20 bees) with alternating warming and cooling periods. Most of the observed bees made one or several long-duration visits (>2 min) to empty cells within the sealed brood area. T(th) at the time bees entered a cell [T(th(entry))] was 34.1-42.5 degrees C (N=40). In 83% of these cell visits, T(th(entry)) was higher (up to 5.9 degrees C; mean 2.5+/-1.5 degrees C; N=33) than the mean T(th) of the same bee. High values of T(th(entry)) resulted from preceding heating activity on the comb surface and from warm-ups just prior to cell visits during which T(th) increased by up to +9.6 degrees C. Bees inside empty cells had mean T(th) values of 32.7+/-0.1 degrees C (resting bees) to 40.6+/-0.7 degrees C (heat-producing bees) during long-duration cell visits without performing any visible work. Heating behaviour inside cells resembles heating behaviour on the brood cap surface in that the bees appear to be inactive, but repeated warmings and coolings occur and T(th) does not fall below the optimum brood temperature. Bees staying still inside empty cells for several minutes have previously been considered to be 'resting bees'. We find, however, that the heating bees can be distinguished from the resting bees not only by their higher body temperatures but also by the continuous, rapid respiratory movements of their abdomens. By contrast, abdominal pumping movements in resting bees are discontinuous and interrupted by long pauses. Heat transfer to the brood from individual bees on the comb surface and from bees inside empty cells was simulated under controlled conditions. Heating on the comb surface causes a strong superficial warming of the brood cap by up to 3 degrees C within 30 min. Heat transfer is 1.9-2.6 times more efficient when the thorax is in touch with the brood cap than when it is not. Heating inside empty cells raises the brood temperature of adjacent cells by up to 2.5 degrees C within 30 min. Heat flow through the comb was detectable up to three brood cells away from the heated thorax.

                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2010
                29 January 2010
                : 5
                : 1
                : e8967
                Affiliations
                [1]Institut für Zoologie, Karl-Franzens-Universität Graz, Graz, Austria
                University of Arizona, United States of America
                Author notes

                Conceived and designed the experiments: AS HK. Performed the experiments: AS HK. Analyzed the data: AS HK RB. Contributed reagents/materials/analysis tools: AS HK. Wrote the paper: AS HK RB.

                Article
                09-PONE-RA-13977R1
                10.1371/journal.pone.0008967
                2813292
                20126462
                34d2ffdb-9d08-47ba-b580-0504ccbbf1ec
                Stabentheiner et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 2 November 2009
                : 11 January 2010
                Page count
                Pages: 13
                Categories
                Research Article
                Physiology
                Ecology/Behavioral Ecology
                Ecology/Physiological Ecology

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                Uncategorized

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