Seasonal effects on thermoregulatory abilities of the Wahlberg's epauletted fruit bat (Epomophorus wahlbergi) in KwaZulu-Natal,South Africa

Seasonal variations in ambient temperature (T_a) require changes in thermoregulatory responses of endotherms. These responses vary according to several factors including taxon and energy constraints. Despite a plethora of studies on chiropteran variations in thermoregulation, few have examined African species. In this study, we used the Wahlberg's epauletted fruit bat (Epomophorus wahlbergi, body mass≈115 g) to determine how the thermoregulatory abilities of an Afrotropical chiropteran respond to seasonal changes in T_a. Mass specific Resting Metabolic Rates (RMR_Ta) and basal metabolic rate (BMR) were significantly higher in winter than in summer. Furthermore, winter body mass was significantly higher than summer body mass. A broad thermoneutral zone (TNZ) was observed in winter (15–35 °C) compared with summer (25–30 °C). This species exhibited heterothermy (rectal and core body temperature) during the photophase (bats' rest-phase) particularly at lower T_as and had a low tolerance of high T_as. Overall, there was a significant seasonal variation in the thermoregulatory abilities of E. wahlbergi. The relative paucity of data relating to the seasonal thermoregulatory abilities of Afrotropical bats suggest further work is needed for comparison and possible effects of climate change, particularly extreme hot days.     

Seasonal variation in thermal energetics of the Australian owlet-nightjar (Aegotheles cristatus)

Many birds living in regions with seasonal fluctuations in ambient temperatures (T_a) typically respond to cold by increasing insulation and adjusting metabolic rate. Seasonal variation in thermal physiology has not been studied for the Caprimulgiformes, an order of birds that generally have basal metabolic rates (BMR) lower than predicted for their body mass. We measured the metabolic rate and thermal conductance of Australian owlet-nightjars (Aegotheles cristatus) during summer and winter using open-flow respirometry. Within the thermoneutral zone (TNZ; 31.3 to 34.8 °C), there was no seasonal difference in BMR or thermal conductance (C), but body temperature was higher in summer- (38.2 ± 0.3 °C) than winter-acclimatized (37.1 ± 0.5 °C) birds. Below the TNZ, resting metabolic rate (RMR) increased linearly with decreasing T_a, and RMR and C were higher for summer- than winter-acclimatized birds. The mean mass-specific BMR of owlet-nightjars (1.27 mL O₂ g^− 1 h^− 1) was close to the allometrically predicted value for a 45 g Caprimulgiformes, but well below that predicted for birds overall. These results suggest that owlet-nightjars increase plumage insulation to cope with low winter T_a, which is reflected in the seasonal difference in RMR and C below the TNZ, rather than adjusting BMR.     

Differences between temperate and tropical birds in seasonal acclimatization of thermoregulatory traits

Phenotypic flexibility can be an important determinant of fitness in variable environments. The climatic variability hypothesis (CVH) predicts that phenotypic flexibility in thermoregulatory traits will be greater in temperate species than tropical species as a means of coping with increased temperature seasonality at higher latitudes. However, support for the CVH has been mixed, and recent studies suggest that tropical birds are capable of substantial phenotypic flexibility. To test the generality of the CVH, we used flow‐through respirometry to quantify seasonal acclimatization in thermoregulatory traits in suites of temperate (n = 6) and tropical (n = 41) birds. We used W/S ratios (winter/summer trait values) to quantify the direction and magnitude of seasonal change (W/S ratio of 1 means no seasonal change). Temperate species exhibited coordinated changes in thermoregulatory traits in winter, including large increases in thermoneutral zone (TNZ) breadth and reductions in heat loss below the lower limit of the TNZ. Conversely, tropical species exhibited idiosyncratic seasonal thermoregulatory responses, and mean W/S ratios were close to 1 for all traits, indicative of little seasonal change and consistent with predictions of the CVH. Nevertheless, mean W/S ratios did not differ significantly between temperate and tropical species for either M_b or BMR, demonstrating that tropical birds can also exhibit substantial thermoregulatory flexibility. Our results highlight the need for complementary acclimation experiments to determine if latitudinal differences in seasonal acclimatization are due to inherent differences in capacity for flexibility.     

The thermal and energetic significance of clustering in the speckled mousebird,Colius striatus

Summary The effect of clustering behaviour on metabolism, body temperature, thermal conductance and evaporative water loss was investigated in speckled mousebirds at temperatures between 5 and 36°C. Within the thermal neutral zone (approximately 30–35 °C) basal metabolic rate of clusters of two birds (32.5 J·g^-1·h^-1) and four birds (28.5 J·g^-1·h^-1) was significantly lower by about 11% and 22%, respectively, than that of individuals (36.4 J·g^-1·h^-1). Similarly, below the lower critical temperature, the metabolism of clusters of two and four birds was about 14% and 31% lower, respectively, than for individual birds as a result of significantly lower total thermal conductance in clustered birds. Body temperature ranged from about 36 to 41°C and was positively correlated with ambient temperature in both individuals and clusters, but was less variable in clusters. Total evaporative water loss was similar in individuals and clusters and averaged 5–6% of body weight per day below 30°C in individuals and below 25°C in clusters. Above these temperatures total evaporative water loss increased and mousebirds could dissipate between 80 and 90% of their metabolic heat production at ambient temperatures between 36 and 39°C. Mousebirds not only clustered to sleep between sunset and sunrise but were also observed to cluster during the day, even at high ambient temperature. Whereas clustering at night and during cold, wet weather serves a thermoregulatory function, in that it allows the brrds to maintain body temperature at a reduced metabolic cost, clustering during the day is probably related to maintenance of social bonds within the flock.Abbreviations BMR basal metabolic rate - bw body weight - C _totab total thermal conductance - EWI evaporative water loss - M metabolism - RH relative humidity - T _a ambient temperature - T _b body temperature - T _ch chamber temperature - T _cl cluster temperature - TEWL total evaporative water loss - LCT lower critical temperature - TNZ thermal neutral zone     

Seasonal adaptation of thermal and metabolic responses in men wearing different clothing at 10° C

Thermoregulatory responses at ambient temperatures of 20 and 10° C in six male subjects wearing two different kinds of clothing were compared between summer and winter. The two different kinds of clothing were one insulating the upper half of the body lightly and the lower half of the body heavily (clothing A, the weight in the upper and lower halves of the body being, respectively, 489 g and 1278 g) and the other insulating the upper half of the body heavily and the lower half of the body lightly (clothing B: 1212 g and 559 g). The major findings are summarized as follow. (i) Rectal temperature was kept significantly higher in clothing B than in clothing A both in summer and winter. (ii) The fall of rectal temperature was significantly greater in summer than in winter in both types of clothing. (iii) Mean skin temperatures and skin temperatures in the face, chest, thigh and leg were significantly lower atT _a of 10° C in summer than in winter in clothing A, while skin temperatures in the face and thigh were also significantly lower atT _a of 10° C in summer than in winter in clothing B. (iv) Metabolic heat production was higher in summer than in winter at 20 and 10° C in both types of clothing. (v) The subjects felt cooler and colder toT _a of 10° C in summer than in winter in both types of clothing. These different responses occurring between summer and winter are discussed mainly in terms of total conductance and dry heat loss.     

Thermoregulation in Malayan sun bears (Helarctos malayanus) and its consequences for in situ conservation

Thermoregulation in Malayan sun bears is not fully understood. Therefore, in this study the effect of meteorological variables on both behavioural and autonomic thermoregulatory mechanisms in sun bears was examined in order to identify temperature thresholds for the activation of various thermoregulatory mechanisms. Infrared thermography was used to non‒invasively determine body surface temperature (T_S) distribution in relation to ambient temperature (T_A) and to determine the thermoneutral zone (TNZ) of sun bears. Thermographic measurements were performed on 10 adult sun bears at T_A between 5 °C and 30 °C in three European zoos. To assess behaviours that contribute to thermoregulation, nine adult sun bears were observed at T_A ranging from 5 °C to 34 °C by instantaneous scan sampling in 60 s intervals for a total of 787 h. Thermographic measurements revealed that the TNZ of sun bears lies between 24 °C and 28 °C and that heat is equally dissipated over the body surface. Behavioural data showed that behaviours related to thermoregulation occurred in advance of energetically costly autonomic mechanisms, and were highly correlated with T_A and solar radiation. While the temperature threshold for the onset of thermoregulatory behaviours below the TNZ lies around 15 °C, which is well below the lower critical temperature (T_LC) assessed by thermography, the onset for behaviours to prevent overheating occurred at 28 °C, which was closer to the estimated upper critical temperature (T_UC) of sun bears. These findings provide useful data on the thermal requirements of sun bears with respect to the species potential to cope with the effects of climate change and deforestation which are occurring in their natural range. Furthermore, these results may have important implications for the care and welfare of bears in captivity and should be taken into consideration, when designing and managing facilities.     

Life in extreme environments: Investigations on the ecophysiology of a desert bird,the Australian Diamond Dove (Geopelia cuneata Latham)

Summary The Diamond Dove, Geopelia cuneata, is the world's second smallest (ca. 35 g) species of the columbid order. The Diamond Dove is endemic in the arid and semiarid Mulga and Spinifex regions of Central and Western Australia. It regularly encounters ambient temperatures (T _a ) in its habitat above +40° C, especially when foraging for seeds on bare ground cover, and may be found at up to 40 km from water. This entails extreme thermal stress, with evaporative cooling constrained by limited water supply. Energy metabolism (M), respiration, body temperature (T _a ) and water budget were examined with regard to physiological adaptations to these extreme environmental conditions. The zone of thermal neutrality (TNZ) extended from +34° C to at least +45° C. Basal metabolic rate (BMR) was 34.10±4.19 J g^–1h^–1, corresponding to the values predicted for a typical columbid bird. Thermal conductance (C) was higher than predicted. Geopelia cuneata showed the typical breathing pattern of doves, a combination of normal breathing at a stable frequency (ca. 60 min^–1) at low T _a and panting followed by gular flutter (up to 960 min^–1) at high T _a . At T _a > +36° C, T _a increased to considerably higher levels without increasing metabolic rate, i.e. Q₁₀=1. This enabled the doves not only to store heat but also to save the amout of water that would have been required for evaporative cooling if T _a had remained constant. The birds were able to dissipate more than 100% of the metabolic heat by evaporation at T _a +44° C. This was achieved by gular flutter (an extremely effective mechanism for evaporation), and also by a low metabolic rate due to the low Q₁₀ value for metabolism during increased T _b . At lower T _a , Geopelia cuneata predominantly relied on non-evaporative mechanisms during heat stress, to save water. Total evaporative water loss over the whole T _a range was 19–33% lower than expected. In this respect, their small body size proved to be an important advantage for successful survival in hot and arid environments.Abbreviations and units Body Mass W (g) - Ambient Temperature T _a (°C) - Body Temperature T _b (°C) - Thermoneutral Zone (TNZ) - Metabolism M (J g^–1 h^–1) - Thermal Conductance C - wet Thermal Conductance C _wet (J g^–1 h^–1 °C^–1) - Evaporative Water Loss EWL (mg H₂O g^–1 h^–1) - Evaporative Heat Loss EHL (J g^–1 h^–1) - Breathing Frequency F (breaths min^–1) - Tidal Volume V _t (ml breath^–1) - Standard Temperature Pressure Dry STPD - Body Temperature Pressure Saturated BTPS - Respiratory Quotient RQ - n.s. not significant (P>0.05) - n number of experiments     

Heat balance of two starling species (Sturnus vulgaris andOnychognathus tristrami) from temperate and desert habitats

Summary Body temperature (T _b), oxygen consumption , thermal conductance (C) and evaporative water loss (EWL) were measured at various air temperatures (T _a) in two starlings which evolved in the tropics: a migratory species from a temperate climate,Sturnus vulgaris, and a resident, desert species,Onychognathus tristrami (Aves, Passeriformes, Sturnidae).AtT _a's of 4–35°C both birds hadT _b of 40.6°C. At 44°C,T _b ofSturnus was 45.8°C and that ofOnychognathus 43.3°C.T _a of 44°C was tolerated only byOnychognathus. The thermoneutral zone (TNZ) ofSturnus was in theT _a range of 29.5°C–36.5°C, that ofOnychognathus 21.5–36.5°C. ofSturnus within its TNZ (BMR) was 2.37 ml O₂ g^–1 h^–1, which is close to the expected BMR; that ofOnychognathus, 1.67 ml O₂ g^–1 h^–1, is only 74% of the expected. AtT _a'sNZ,C ofSturnus was twice as high as that ofOnychognathus and 1.68 times the expected value, whereasC ofOnychognathus was only 94% of the expected. At highT _a'sOnychognathus had higherC thanSturnus. At either low or highT _a's EWL ofSturnus was greater than ofOnychognathus.The responses shown bySturnus are typical of a tropical bird living in a moderate environment. This indicates that neither in USSR where it spends the summer, nor in Israel where it spends the winter, is this starling exposed to extreme temperatures.Onychognathus is better adapted not only to high but also to the low temperatures prevailing in mountainous regions of the desert.Symbols and abbreviations BMR basal metabolic rate - C thermal conductance - EWL evaporative water loss - HE evaporative heat loss - HP heat production - TNZ thermoneutral zone     

Preferred ambient temperature for old and young men in summer and winter

To investigate the effects of age on thermal sensitivity, preferred ambient temperature (T _pref) was compared between old (71–76 years) and young (21–30 years) groups, each consisting of six male subjects in summer and winter. The air temperature (T _a) was set at either 20° C or 40° C at commencement. The subject was directed to adjust theT _a for 45 min by manipulating a remote control switch to the level at which he felt most comfortable. In the older group, theT _pref was significantly lower in trials starting at 20° C than that starting at 40° C in summer. The fluctuation ofT _pref (temperature difference between maximum and minimumT _a during the last 10 min) was significantly wider in the older group in both summer and winter. Repetition of the same experiment on each subject showed a poorer reproducibility ofT _pref in the older group than in the younger group in summer. Tympanic and esophageal temperatures of the older group kept falling throughout the trial starting at 20° C in summer. These results suggest that thermal sensitivity is decreased with advancing age and that thermal perception in the elderly, especially to cold, is less sensitive in summer.     

Seasonal effects on the thermoregulation of invasive rose-ringed parakeets (Psittacula krameri)

Invasive species are a major threat to global biodiversity. Rose-ringed parakeets Psittacula krameri are widely established outside their native range and are successful invaders in many countries, including South Africa. Physiological and behavioral responses to environmental conditions are considered to be major factors that influence the abundance and distribution of birds. As rose-ringed parakeets are able to tolerate wide varieties of climatic conditions as invaders, it is important to understand their physiological responses to these. This study examined the effects of seasonal changes in ambient temperatures (T_a) on metabolic rate and body temperature (T_b) of captive-bred rose-ringed parakeets. Resting metabolic rate at various T_a and basal metabolic rate were significantly lower in winter compared to summer, and the thermo-neutral zone was broader in winter than in summer. There was no significant difference in body mass (M_b) between seasons. These parakeets showed seasonal thermoregulatory responses that represented energy conservation as expected, rather than cold tolerance. They were relatively tolerant of low T_a and showed no hypothermia at 5 °C. Our results suggest that this species is physiologically and behaviorally equipped to cope with a range of climatic situations and this partly explains their global success as an invader species.     

Energy relations of winter roost-site utilization by American goldfinches (Carduelis tristis)

Summary American goldfinches (Carduelis tristis) were observed roosting in Colorado blue spruce (Picea pungens), which comprised part of a mixed stand of conifers. Their winter roost-sites were distally situated among the most densely-needled branches on the leeward sides of these trees. Heated and unheated taxidermic goldfinch mounts were placed within these sites and at the same height in an adjacent clearing. The radiative and convective characteristics of these locations were monitored simultaneously and compared to predicted power requirements of live goldfinches (based on laboratory calibration of heated mounts) and operative temperatures (T _e ; based on body temperatures of unheated mounts). The winter roost-sites significantly reduced radiative and convective heat exchanges between goldfinches and the environment. Based on body composition data for winter goldfinches, all but two birds sampled could endure a 15-h roost period at average overnight T _e 's as low as-40°C. In contrast, if these birds were prevented from feeding the following day, only 30% could survive the imposition of a 39-h fast at average T _e 's of-2°C. Winter roost-site selection may be more constrained by thermoregulatory considerations in small birds than in larger species.     

Nest insulation: Energy savings to brown lemmings using a winter nest

Summary Energy metabolism of brown lemmings in summer pelage was measured over long periods at several air temperatures, with and without a real nest or artificial nest material. Resting metabolism of lemmings at T _a=-16°C was 43% higher than that of lemmings in nests. As T _a increased, the difference between resting metabolism of animals with and without nests decreased and was similar at T _a=20°C. The energy saved at rest is equivalent to a reduction of approximately 40% in the thermal conductance. Independent estimates of energy savings due to nest insulation by analysis of cooling curves of a lemming model with and without a nest suggest a 46% reduction in thermal conductance due to the nest. At T _a=0°C, baby lemmings huddled in a nest had equilibrium temperature excesses (T _b-T _a) four to five times higher than isolated nestlings outside the nest. These data indicate that there is a substantial energy savings at ecologically relevant air temperatures, and that energy savings increase as T _a decreases. If the insulative value of the nest is similar whether the animal is in summer or winter pelage, these data suggest that heat production of a resting lemming would be 0.88 W (about 1.6 times BMR), while in nests at subnivean air temperatures typical of Barrow, Alaska, during the winter.     

The roles of energetics,water economy,foraging behavior,and geothermal refugia in the distribution of the bat,Macrotus californicus

Summary Energy metabolism, thermoregulation, and water flux ofMacrotus californicus, the most northerly representative of the Phyllostomidae, were studied in the laboratory using standard methods, and energy metabolism and water fluxes were studied in the field using the doubly labelled water method together with a time budget. Daily energy expenditures of free-living bats averaged 22.8 kJ during the winter study period. Approximately 60% of this was allocated to resting metabolism costs while in the primary roosts (22 h/day).Macrotus californicus is unable to use torpor. The thermoneutral zone (TNZ) in this species is narrow (33 to 40 °C) and metabolic rate increased rapidly as ambient temperature decreased below the TNZ. Basal metabolic rate was 1.25 ml O₂/g·h, or 24 J/g·h. Total thermal conductance below the TNZ. was 1.8 mW/g·°C, similar to values measured for other bats. Evaporative water loss showed a hyperbolic increase with increasing ambient temperature, and was approximately 1% of total body mass/h in the TNZ. The success of these bats as year-round residents in deserts in the southwestern United States is probably not due to special physiological adaptations, but to roosting and foraging behavior. They use geothermally-heated winter roost sites (stable year-round temperatures of approximately 29 °C) which minimize energy expenditures, and they have an energetically frugal pattern of foraging that relies on visual prey location. These seem to be the two major factors which have allowedM. californicus to invade the temperate zone.Abbreviations BMR basal metabolic rate - FMR field metabolic rate - T _a ambient temperature - T _b body temperature - T _lc,T _uc lower and upper critical temperature, respectively - TBW total body water - TNZ thermoneutral zone     

Seasonal control of energy requirements for thermoregulation in the djungarian hamster (Phodopus sungorus), living in natural photoperiod

Summary Djungarian dwarf hamsters,Phodopus s. sungorus, were kept in natural photoperiodic conditions throughout the year, either inside at a constantT _a of 23°C or outside subjected to seasonally varyingT _a. Comparisons were made between hamsters from both conditions to evaluate the significance of seasonal changes in photoperiod and/orT _a as environmental cues for seasonal acclimatization inPhodopus. Basal metabolic rate was lowest in July (1.68 ml/g·h) and highest in January (2.06 ml/g·h inPhodopus living outside), combined with a decrease inT _1c from 26°C in July to 20°C in January. This was parallelled by seasonal changes in body weight (summer 42 g, winter 25g), fur colouration, fur depth and the occurrence of short daily torpor.AtT _a below thermoneutrality total energy requirements for thermoregulation in winter acclimatizedPhodopus were found 36% lower than summer values (e.g. at O°CT _a in summer 1,160 mW, in winter 760 mW), which were effected by a combined strategy of reducing body weight (19%) together with improvements of thermal insulation of the body surface (17%). All seasonal changes were similar inPhodopus living inside or outside, suggesting that seasonal changes in photoperiod and not seasonal changes inT _a is the overriding controller for the environmental cueing of seasonality in energy requirements for thermoregulation.This research was supported by the Deutsche Forschungsgemeinschaft (He 990)     

Daily rhythm of oxygen consumption and thermoregulatory responses in some European winter- or summer-acclimatized finches at different ambient temperatures

The oxygen consumption of European finches, the siskin (Carduelis spinus), the brambling (Fringilla montifringilla), the bullfinch (Pyrhulla pyrhulla), the greenfinch (Carduelis chloris) and the hawfinch (Coccothraustes coccothraustes), was recorded continuously while ambient temperature was decreased stepwise from +30 down to-75°C. The oxygen consumption, body temperature (telemetrically), and shivering (integrated pectoral electromyography) of greenfinches were measured simultaneously at ambient temperatures between +30 and-75°C. Maximum heat production, cold limit, lower critical temperature, basal metabolic rate and thermal conductance (of the greenfinch) were determined. The diurnal variation of oxygen consumption of siskins and greenfinches was recorded at thermoneutrality and below the thermoneutral zone in winter- and summer-acclimatized birds. The diurnal variation of body temperature and thermal conductance of greenfinches were also determined. The diurnal variation of heat production was not seasonal or temperature dependent in the siskin and in the greenfinch. Nocturnal reduction of oxygen consumption saved 15–33% energy in the siskin and greenfinch. Body temperature of the greenfinch was lowered by 2.5–3.4°C. The nocturnal reduction of thermal conductance in the greenfinch was 39–48%. The basal metabolic rate was lowest in the largest bird (hawfinch) and highest in the smallest bird (siskin). The values were in the expected range. The heat production capacity of finches in winter was 4.7 times basal metabolic rate in the siskin, 4.2 times in the brambling, 3.5 times in the greenfinch and 2.9 times in the bullfinch and hawfinch. The heat production capacity of the siskin and greenfinch was not significantly lower in summer. The cold limit temperatures (°C) in winter were-61.2 in the siskin,-41.3 in the greenfinch,-37.0 in the bullfinch,-35.7 in the brambling and-28.9 in the hawfinch. The cold limit was 14.3°C higher in summer than in winter in the siskin and 8.7°C in the greenfinch. Thermal insulation of the greenfinch was significantly better in winter than in summer. The shivering of the greenfinch increased linearly when ambient temperature was decreased down to-40°C. Maintenance of shivering was coincident with season. In severe cold integrated pectoral electromyography did not correlate with oxygen consumption as expected. The possible existence of non-shivering thermogenesis in birds is discussed. It is concluded that the acclimatization of European finches is primarily metabolic and only secondly affected by insulation.Abbreviations AAT avian adipose tissue - bm body mass - BMR basal metabolic rate - C _t thermal conductance - EMG electromyogram - HP heat production - HP _max maximum heat production - MR metabolic rate - NST non-shivering thermogenesis - RMR resting metabolic rate - RQ respiratory quotient - T _a ambient temperature - T _b body temperature - T _c colonic temperature - T _1c lower critical temperature - TNZ thermoneutral zone - T _st shivering threshold temperature - V oxygen consumption     

Thermoregulation in leopard tortoises in the Nama-Karoo: The importance of behaviour and core body temperatures

Despite being ectotherms, reptiles have an ability to thermoregulate which is enhanced by adopting a variety of behavioural mechanisms. Different behavioural postures, the use of retreat sites and selection of microhabitats enable reptiles to maintain their core body temperatures (T_b) above that of ambient temperatures (T_a) in winter or below T_a maximum in summer. This study describes the daily activity patterns of leopard tortoises (Stigmochelys pardalis) in relation to T_b and T_a, and the extent to which leopard tortoises can manipulate their T_b in response to seasonal changes in T_a. Ten and nine leopard tortoises were radio-tracked in 2002 and 2003, respectively and cloacal T_b and behaviours observed. Core T_bs were measured using Thermocron iButtons^™ surgically implanted into the body cavities of 4 and 5 adult telemetered tortoises for summer and winter 2003, respectively. There were seasonal differences in the extent to which certain behaviours were practiced and the time of day that these occurred. Leopard tortoises generally had unimodal activity patterns in winter and bimodal ones in summer. In winter tortoises were active at lower T_bs, and at lower T_a, than in summer. Tortoises maintained their core T_b well below T_a minimum profiles in summer and well above these in winter. Core T_b closely followed the increase in T_a minimum profiles in the mornings, however tortoises exhibited an extended thermal lag when T_a minimum profiles cooled overnight. By using different behavioural mechanisms in summer and winter, leopard tortoises maintained their core T_b at different levels compared with T_a minimum and maximum profiles. Consequently although they are ectotherms, they maintained their core T_b independent of T_a.     

Thermoregulation of water foraging honeybees—Balancing of endothermic activity with radiative heat gain and functional requirements

Foraging honeybees are subjected to considerable variations of microclimatic conditions challenging their thermoregulatory ability. Solar heat is a gain in the cold but may be a burden in the heat. We investigated the balancing of endothermic activity with radiative heat gain and physiological functions of water foraging Apis mellifera carnica honeybees in the whole range of ambient temperatures (T_a) and solar radiation they are likely to be exposed in their natural environment in Middle Europe.The mean thorax temperature (T_th) during foraging stays was regulated at a constantly high level (37.0-38.5 °C) in a broad range of T_a (3-30 °C). At warmer conditions (T_a = 30-39 °C) T_th increased to a maximal level of 45.3 °C. The endothermic temperature excess (difference of T_body − T_a of living and dead bees) was used to assess the endogenously generated temperature elevation as a correlate of energy turnover. Up to a T_a of ∼30 °C bees used solar heat gain for a double purpose: to reduce energetic expenditure and to increase T_th by about 1-3 °C to improve force production of flight muscles. At higher T_a they exhibited cooling efforts to get rid of excess heat. A high T_th also allowed regulation of the head temperature high enough to guarantee proper function of the bees’ suction pump even at low T_a. This shortened the foraging stays and this way reduced energetic costs. With decreasing T_a bees also reduced arrival body weight and crop loading to do both minimize costs and optimize flight performance.     

Patterns of heat response and adaptation on summer pasture: A comparison of heat-sensitive (Angus) and -tolerant (Romosinuano) cattle

Heat stress in Bos taurus cattle is a problem that affects many regions of the world. Numerous studies have focused on heat stress in feedlots or environmental chambers; but few have looked at undisturbed cattle on pasture. The present study followed two Bos taurus cattle breeds throughout a mid-Missouri summer to determine thermoregulatory responses to fluctuating summer air temperature (T_a), as well as differences in adaptation to heat. Heat-sensitive Angus steers (ANG; n=22; 480±7.15 kg BW), and heat-tolerant Romosinuano steers (RO; n=11; 352±6 kg BW) were monitored on 12 day from June through August of 2009 in an endophyte free tall fescue pasture. Data were grouped into two, six-day periods representing peak (Period 1) and late (Period 2) summer for determination of adaptation. Respiration rate (RR) was measured via flank counting and telemetric temperature transmitters in the rumen of each animal monitored core temperature (T_rum). Romosinuano sustained a lower (P<0.05) RR and T_rum compared to ANG during both periods. Linear relationships for RR and T_rum, compared against T_a for both Periods were determined. Slopes of RR to T_a from Period 1 to Period 2 decreased (P<0.05) from 2.63 to 1.08 bpm/°C and 2.25 to 0.49 bpm/°C for ANG and RO, respectively. Slopes of T_rum to T_a also decreased (P<0.05) from Periods 1 to 2 from 0.12 to 0.02 °C T_rum/°C T_a for ANG; however, RO showed no differences between periods. Although Romosinuano have a lower respiration rate and ruminal temperature than Angus, they share a similar pattern of respiration rate adaptation from early to late summer periods.     

Metabolic thermogenesis and evaporative water loss in the Hwamei Garrulax canorus

Basal metabolic rate (BMR) is thought to be a major hub in the network of physiological mechanisms connecting life history traits. Evaporative water loss (EWL) is a physiological indicator that is widely used to measure water relations in inter- or intraspecific studies of birds in different environments. In this study, we examined the physiological responses of summer-acclimatized Hwamei Garrulax canorus to temperature by measuring their body temperature (T_b), metabolic rate (MR) and EWL at ambient temperatures (T_a) between 5 and 40 °C. Overall, we found that mean body temperature was 42.4 °C and average minimum thermal conductance (C) was 0.15 ml O₂ g⁻¹ h⁻¹ °C⁻¹ measured between 5 and 20 °C. The thermal neutral zone (TNZ) was 31.8–35.3 °C and BMR was 181.83 ml O₂ h⁻¹. Below the lower critical temperature, MR increased linearly with decreasing T_a according to the relationship: MR (ml O₂ h⁻¹)=266.59–2.66 T_a. At T_as above the upper critical temperature, MR increased with T_a according to the relationship: MR (ml O₂ h⁻¹)=−271.26+12.85 T_a. EWL increased with T_a according to the relationship: EWL (mg H₂O h⁻¹)=−19.16+12.64 T_a and exceeded metabolic water production at T_a>14.0 °C. The high T_b and thermal conductance, low BMR, narrow TNZ, and high evaporative water production/metabolic water production (EWP/MWP) ratio in the Hwamei are consistent with the idea that this species is adapted to warm, mesic climates, where metabolic thermogenesis and water conservation are not strong selective pressures.     

Ventilation and oxygen consumption inAmazona viridigenalis

Summary The BMR (6.00 ml O₂·min^–1) and thermal conductance (0.235 ml O₂·min^–1·°C^–1) ofAmazona viridigenalis, a medium sized parrot, are close to allometrically predicted values for nonpasserine birds, but theT _1c of 26.5 °C is 8.5 °C higher than predicted (Fig. 1). Minimal respiratory frequencies measured in four species of birds average 60% of the rate predicted by a previous equation and yield the relationship, breaths·min^–1= 10.3 kg^–0.32. Frequencies are very dependent upon the methods used to obtain the data (Fig. 3). Resting values of respiratory parameters are poorly defined in the existing literature, and there are no single resting values within the TNZ analogous to a BMR. Rather values change within, as well as below and above, the TNZ. Minimal values of different parameters occur at differentT _a's, not necessarily within the TNZ (Figs. 2, 4, 5). For clarity, resting respiratory parameters should be reported as standard values, analogous to standard metabolic rates, withT _a specified. In birds the pattern of ventilation (f andV _T) changes asT _a changes resulting in different extraction efficiencies at a given minute volume (Figs. 6, 7). This facilitates adjustment to both changing oxygen demands and changing thermoregulatory needs.Abbreviations and symbols BMR basal metabolic rate - TNZ thermoneutral zone - T _a ambient temperature - SMR standard metabolic rate - R.H. relative humidity - f respiratory frequency - br breath - T _b body temperature - T _lc lower critical temperature - Tuc upper critical temperature - T _Rlc respiratory lower critical temperature - RQ respiratory quotient - extraction efficiency - V _T tidal volume - minute volume (=V _T xf)