Effects of body mass,temperature, and season on resting metabolism of the nocturnal gecko Hemidactylus flaviviridis

Abstract

The resting metabolic rate (RMR) of Hemidactylus flaviviridis was measured at different temperatures from 20 to 35°C during winter and summer acclimatization. The mass exponent b values ranged between 0.67 and 0.72. Winter-acclimatized geckos of various body masses had significantly lower RMRs than summer-acclimatized geckos only at 20°C. It seems that low thermal sensitivity for summer–acclimatized group may facilitate activity during its active seasons, and high thermal sensitivity between 20 and 25°C for winter–acclimatized group may conserve energy during inactivity in winter.     

Shifts in thermal preference of introduced Asian house geckos (Hemidactylus frenatus) in temperate regions of southeastern Australia

Despite its tropical origin, the Asian house gecko (Hemidactylus frenatus) is currently invading higher latitudes around the world. In this study, we investigated whether the introduced geckos in the subtropical/temperate region of southeastern Australia have shifted their thermal biology to cope with colder temperatures. In the lab, we measured the body temperatures of geckos from Thailand and Australia in a cost-free thermal gradient. Native H. frenatus from Thailand displayed a diel pattern of thermoregulation. Geckos maintained higher body temperatures during mid-afternoon and at dusk but selected cooler temperatures during the night. Introduced geckos showed a similar pattern of thermoregulation, but selected lower body temperatures in summer (mean = 28.9 °C) and winter (mean = 25.5 °C) than native geckos (mean = 31.5 °C). While the Asian house geckos from Thailand did not alter their body temperatures after feeding, their conspecifics from southeastern Australia selected body temperatures that were 1.6–3.1 °C higher after feeding. In conclusion, our study shows that invasive house geckos in Australia have shifted their preferred body temperatures downwards relative to their native conspecifics in Thailand, presumably as a result of plasticity or natural selection. Our findings suggest that these tropical geckos have adapted to colder regions, and thus, they may spread much further than expected for a tropical ectotherm.     

The influence of temperature,sexual condition,and season on the metabolic rate of the lizardPsammodromus hispanicus

Summary Male and femalePsammodromus hispanicus from southern Europe were acclimated to four seasonal conditions of photoperiod and night time temperature. During the dark period, the lizards' body temperatures fell to ambient air temperature but during the light period the lizards were allowed to thermoregulate behaviourally and at such times the lizards' mean body temperature varied from 29.0°C to 32.6°C. The resting metabolic rate of these lizards was measured in 5°C steps from 5°C to 30°C or 35°C. Sexual condition had little effect on resting metabolic rate, but at low temperatures lizards acclimated to winter or spring seasonal conditions had lower resting metabolic rates than those acclimated to summer or autumn conditions. At temperatures above 20°C seasonal acclimation had no effect on resting metabolic rate. It is considered that the reduction in low temperature metabolic rate in spring and winter is induced by low night time temperatures and serves to conserve energy during those seasons when lizards must spend long periods at low temperature without being able to feed.     

Energetics and water flux of the marbled velvet gecko (Oedura marmorata) in tropical and temperate habitats

The gecko Oedura marmorata was studied in two different climatic zones: the arid zone of central Australia and in the wet-dry tropics of northern Australia. Doubly labelled water was used to measure field metabolic rate (FMR) and water flux rates of animals in the field during the temperate seasons of spring, summer and winter, and during the tropical wet and dry seasons. FMRs were highest in the tropical wet season and lowest in the temperate winter. The geckos in central Australia expended less energy than predicted for a similarly sized iguanid lizard, but geckos from the tropics expended about the same amount of energy as predicted for an iguanid. Water flux rates of geckos from the arid zone were extremely low in all seasons compared to other reptiles, and although water flux was higher in tropical geckos, the rates were low compared to other tropical reptiles. The standard metabolic rates (SMRs) of geckos were similar between the two regions and among the seasons. Geckos selected higher body temperatures (T _bs) in a laboratory thermal gradient in the summer (33.5°C) and wet (33.8°C) seasons compared to the winter (31.7°C) and dry (31.4°C) seasons. The mean T _bs selected in the laboratory thermal gradient by geckos from the two regions were not different at a given time of year. The energy expended during each season was partitioned into components of resting metabolism, T _b and activity. Most of the energy expended by geckos from central Australia could be attributed to the effects of temperature on resting lizards in all three seasons, but the energy expended by tropical geckos includes a substantial component due to activity during both seasons. This study revealed variability in patterns of ecological energetics between populations of closely related geckos, differences which cannot be entirely attributed to seasonal or temperature effects. Received: 14 November 1997 / Accepted: 4 May 1998     

Rate of metabolism in the smallest simian primate,the pygmy marmoset (Cebuella pygmaea)

Rate of metabolism was measured with six adult pygmy marmosets (Cebuella pygmaea) at regulated ambient temperatures ranging between 20°C and 35°C. A novel combined nest box and metabolic chamber was designed to allow nighttime measurements on immobile animals in their home cage without disturbance. The basal rate of metabolism (BMR) was 98 ml O₂ h⁻¹, representing 74% of the value expected from the equation of McNab [Quarterly Review of Biology 63:25–54, 1988] relative to body mass. The thermoneutral zone was approximately 27–34°C. Below the lower critical temperature (27–28°C), thermal conductance (12.9 ml O₂ h⁻¹ °C⁻¹) was close to the predicted value. Body temperature ranged between 34.9°C and 35.5°C at night. When two animals rested together overnight in the nest box, the lower critical temperature was slightly lowered, and individual energy expenditure at 20–21°C was reduced by about 34%. The basal rate of metabolism of C. pygmaea is much lower than reported in an earlier study based on daytime measurements but agrees with values reported from a more recent study conducted at night with a classical metabolic chamber. In order to compare the BMR of C. pygmaea with that of other primates, 23 species were included in a comparative study taking into account both phylogeny and body mass (independent contrasts approach). The scaling exponent of BMR to body mass obtained was indistinguishable from that published for eutherian mammals in general. Cebuella and Callithrix exhibit the lowest basal rates known for simians. This trait may possibly be linked to the natural diet, which includes a large proportion of gums that are difficult to digest, but additional metabolic studies on primates are needed for further examination of its adaptive significance. Am. J. Primatol. 41:229–245, 1997. © 1997 Wiley-Liss, Inc.     

Thermal tolerance and standard metabolic rate of juvenile gilthead seabream (Sparus aurata) acclimated to four temperatures

Temperature variation affects the growth, maturation and distribution of fish species due to increasing constraints on physiological functions therefore, the aim of the present study is to evaluate effect of temperature on thermal tolerance and standard metabolic rate (SMR) of gilthead seabream (Sparus aurata). For this purpose, tolerable temperature ranges of juvenile gilthead seabream acclimated at 15, 20, 25, and 30 °C for 30 days were estimated using dynamic and static thermal methodologies. The SMRs of the fish were also determined based on oxygen consumption rate (OCR). The dynamic and static thermal tolerance zones of gilthead seabream were calculated as 737 °C² and 500 °C², respectively, with a resistance zone area of 155.5 °C². The SMR of the fish at the above acclimation temperatures (AT) was determined as 138, 257, 510, and 797 mg O₂ h⁻¹ kg⁻¹, respectively and were significantly different (P < 0.01, n = 10). The temperature quotient (Q₁₀) in relation to the SMR of the fish was calculated as 3.45, 3.91, and 2.44 for acclimation temperature ranges of 15–20, 20–25, and 25–30 °C, respectively. The fact that the SMR increased with rising temperatures and then decreased gradually after 25 °C indicates that the temperature preference of juvenile gilthead seabream lies between 25 and 30 °C. This study shows that gilthead seabream tolerates a relatively narrow temperature range, and consequently, a low capacity for acclimatisation to survive in aquatic systems characterised by temperature variations.     

The thermal biology of the white-tailed rat Mystromys albicaudatus,a cricetine relic in southern temperate African grassland

This study examines the hypothesis that Mystromys albicaudatus, a cricetine relic in southern Africa, has thermal characteristics typical of a rodent adapted to a cold temperature regime. Metabolic rate (oxygen consumption) of M. albicaudatus was measured using open-flow respirometry at ambient temperatures ranging from 5°C to 35°C. Lowest specific oxygen consumption was 1.352 ± 0.089 ml O₂ g⁻¹hr⁻¹ (n = 8; body mass = 93.78 ± 6.27 g) at 25°C, equivalent to 121.8% of the predicted value of Kleiber (1975), 128.8% of the value predicted for eutherians and 113.7% of the value predicted for cricetidae (Hayssen and Lacy, 1985).     

Body temperature and time of day both affect nocturnal lizard performance: An experimental investigation

The locomotor performance of reptiles is profoundly influenced by temperature, but little is known about how the time of day when the animal is usually active may influence performance. Time of day may be particularly relevant for studies on nocturnal reptiles that thermoregulate by day, but are active at night when ambient temperatures are cooler. If selection favours individuals that match their performance to activity times, then nocturnal species should perform better during the night, when they are normally active, than during the day. To test this hypothesis, we investigated how the time of day and body temperature affected the locomotor performance of adult females of the velvet gecko (Amalosia lesueurii). We measured the sprint speeds, running speeds and number of stops of 43 adult females at four different body temperatures (20, 25, 30 and 35 °C) during the day and at night. At night, sprint speeds were higher at 20 and 35 °C but sprint speeds were similar at 25 and 30 °C. By day, sprint speed increased with body temperature, peaking at 30 °C, before declining at 35 °C. However, gecko speeds over 1 m was higher at night at all four test temperatures than by day. Number of stops showed broadly similar patterns and females stopped almost twice as often on the racetrack during the day than they did at night. Furthermore, the thermal breadth of performance differed depending on when geckos were tested. Our results demonstrate that both body temperature and the time of day affects the behaviour and locomotor performance of female velvet geckos, with geckos running faster at night, the time of day when they are usually active. This study adds to evidence that both body temperature and the time of day are crucial for estimating the performance of ectotherms and evaluations and predictions of their vulnerability to climate warming should consider the context of laboratory experimental design.     

Survival of Heleomyza borealis (Diptera, Heleomyzidae) larvae down to − 60°C

Heleomyza borealis Boh. (Diptera, Heleomyzidae) overwinters as larvae in Arctic habitats, where they may experience winter temperatures below ? 15°C. The larvae freeze at c.? 7°C but in acclimation experiments 80% survived when exposed to ? 60°C. Of the larvae exposed to between ? 4 and ? 15°C, only 3% pupated. However, when cooled to ? 20°C this increased to 44%, with 4% emerging as adults. Larvae maintained at 5°C contained low levels of glycerol, sorbitol and trehalose, which did not increase with acclimation to low temperatures. However, levels of fructose increased from 6.1 μg mg^?1 fw in control animals to 17 μg mg^?1 fw when exposed to ? 2°C for 1 week. Larval body water (2.2 ± 0.1 g/g dw, mean ± SD, n = 100) and lipid content (0.22 ± 0.002 g/g fw, mean ± SE) showed no significant change during acclimation to low temperatures. Larvae maintained at a constant 5°C survived for over 18 months with little loss of body mass (from 7.5 ± 1.2 to 7.0 ± 1.2 mg fw, mean ± SD, n = 20), but none pupated. Heleomyza borealis larvae appear to feed and grow until they reach a body mass of about 7.5 mg and then become dormant. They remain in this state until they experience a low temperature stimulus (< ? 15°C) followed by a warm period (≈ 5°C). This ensures that the larvae pupate and adults emerge in early summer, allowing the maximum growing period before the following winter. Heleomyza borealis are adapted to survive long winters in a dormant larval state. They have a low metabolic rate, can conserve body water even at subzero temperatures but do not synthesize large quantities of cryoprotectants.     

Versuche über die Abhängigkeit der Atmung vonArenicola marina (Annelides Polychaeta) von Größe und Temperatur

A knowledge of the rate of oxygen consumption is very important for the evaluation of many physiological and ecological problems. Among the many factors affecting respiratory rate, water temperature and body size are particularly considered here. The modifying effects of body size may be expressed mathematically by the allometric formula: y=b · w ^a , where b represents the rate of O₂ consumption of an individual whose weight is expressed in a chosen metrical weight unity (i. e. in grams, ounces, etc.), anda represents the decrease of metabolic rate during growth. InArenicola the exponent is not the same at all temperatures tested. In most cases it lies between 0.7 and 0.8, i. e., between a weight proportional respiratory rate and a surface proportional one. Minimum values fora were found in experiments conducted in summer at 20° C and in spring at 15° C. They characterize an optimum efficiency of metabolism at these temperatures. Determinations of b demonstrated that metabolic rate ofArenicola is significantly less affected in spring (10° to 20° C) and autumn (10° to 25° C) than is usually known from biological processes. However, the temperature coefficients above and below these temperature ranges are very high. Another break in the temperature-rate curve could be demonstrated below 5° C in spring.     

The thermoregulatory limits of an Australian Passerine,the Silvereye (Zosterops lateralis)

(1) The thermal capabilities of Australian silvereyes (Zosterops lateralis, 11 g) were investigated both at low and high ambient temperatures (T_a) during the photophase and scotophase. (2). The peak metabolic rate (PMR) induced by helium–oxygen (79:21 %, He–O₂) exposure during the photophase was 15.64±1.55 mL O₂ g⁻¹ h⁻¹ at an effective lower survival limit T_a (T_pmr) of −39.7±6.1°C. (3). Above the thermoneutral zone (TNZ), metabolic rate, body temperature (T_b), and thermal conductance increased steeply, but they were able to withstand a T_a of 39°C. (4). Our study shows that silvereyes are able to tolerate an impressive range of T_a from about −42°C to at least +39°C and are able to produce enough heat to maintain a thermal difference between T_b and T_a of up to 80°C.     

Nocturnal loss of body reserves reveals high survival risk for subordinate great tits wintering at extremely low ambient temperatures

Winter acclimatization in birds is a complex of several strategies based on metabolic adjustment accompanied by long-term management of resources such as fattening. However, wintering birds often maintain fat reserves below their physiological capacity, suggesting a cost involved with excessive levels of reserves. We studied body reserves of roosting great tits in relation to their dominance status under two contrasting temperature regimes to see whether individuals are capable of optimizing their survival strategies under extreme environmental conditions. We predicted less pronounced loss of body mass and body condition and lower rates of overnight mortality in dominant great tits at both mild and extremely low ambient temperatures, when ambient temperature dropped down to ?43 °C. The results showed that dominant great tits consistently maintained lower reserve levels than subordinates regardless of ambient temperature. However, dominants responded to the rising risk of starvation under low temperatures by increasing their body reserves, whereas subdominant birds decreased reserve levels in harsh conditions. Yet, their losses of body mass and body reserves were always lower than in subordinate birds. None of the dominant great tits were found dead, while five young females and one adult female were found dead in nest boxes during cold spells when ambient temperatures dropped down to ?43 °C. The dead great tits lost up to 23.83 % of their evening body mass during cold nights while surviving individuals lost on average 12.78 % of their evening body mass. Our results show that fattening strategies of great tits reflect an adaptive role of winter fattening which is sensitive to changes in ambient temperatures and differs among individuals of different social ranks.     

The effect of size and temperature on the frequency of limb beat of Temora longicornis Müller (Crustacea : Copepoda)

Copepods normally swim by rhythmically beating the cephalic limbs, so records of antennal movements represent their activity. The limb beat rate of Temora longicornis Müller was determined in relation to several factors. There was an inverse relationship between swimming rate and body size, and activity increased with environmental temperature up to 20–25°C. Copepods readily acclimated, as those kept at 15°C were less active than those kept at 5°C. The summer population was also less active in the low temperature range, but swimming reached a higher rate at higher temperatures than were tolerated by the winter population. No difference in rate of limb beat was found between similar sized males and females over a wide range of temperatures.     

Ecological physiology of arctic marine invertebrates. Temperature and salinity relationships of the amphipod Onisimus affinis H. J. Hansen

Effects of temperature and salinity upon the survival, locomotion and metabolism of the Arctic marine amphipod Onisimus affinis H. J. Hansen have been investigated. The LD₅₀ for temperature is ≈ 18.7 °C. The metabolic rate-temperature curve shows a distinct plateau of relative temperature insensitivity the position of which varies seasonally to include a lower temperature range in winter than in summer. Similar shifts in the plateau can be induced in the laboratory by acclimating the animals at summer- and winter-like temperatures.Optimal locomotory activity was between 5° and 8 °C and included a combination of swimming and crawling. Above 12 °C the swimming component was increasingly inhibited.Onisimus is euryhaline and appears to be most successful in brackish water habitats. It tolerates elevated salinities better at low temperatures. The metabolic rate varies inversely with salinity during short-term exposures, but, if the animals are pre-adapted to the experimental salinities for 10 days, the metabolic rate is essentially independent of salinity between 10%. and 25%.The significance of these physiological responses in relation to the general ecology of the species is discussed.     

That’s hot: golden spiny mice display torpor even at high ambient temperatures

Golden spiny mice (Acomys russatus) living in the Judean desert are exposed to extended periods of food and water shortage. We investigated their thermal and metabolic response to three weeks of 50 % food reduction at ambient temperatures of 23, 27, 32 and 35 °C by long term records of metabolic rate and body temperature in the laboratory. At all ambient temperatures, A. russatus responded to starvation by a reduction of daily energy expenditure. At 32 and 35 °C, this metabolic adjustment fully compensated the reduced food availability and they maintained their energy balance at a slightly reduced body mass. At lower ambient temperatures, they could not fully compensate for the reduced food availability and kept a negative energy balance. The reduction of daily energy expenditure was largely achieved by the occurrence of daily torpor. Torpor even occurred at high ambient temperatures of 32 and 35 °C during which metabolic depression was not associated with a marked decrease of body temperature. The results show that the occurrence of daily torpor is not necessarily linked to cold exposure and the development of a pronounced hypothermia, but may even occur as depression of metabolic rate in a hot environment.     

Turning up the heat on subzero fish: thermal dependence of sustained swimming in an Antarctic notothenioid

We determined the maximum sustained swimming speed (U_crit), and resting and maximum ventilation rates of the Antarctic fish Pagothenia borchgrevinki at five temperatures between −1°C and 8°C. We also determined resting metabolic rate (VO₂) at −1°C, 2°C, and 4°C. U_crit of P. borchgrevinki was highest at −1°C (2.7±0.1 BL s⁻¹) and rapidly decreased with temperature, representing a thermal performance breadth of only 5°C. This narrow thermal performance supports our prediction that specialisation to the subzero Antarctic marine environment is associated with a physiological trade-off in performance at high temperatures. Resting oxygen consumption and ventilation rate increased by more than 200% across the temperature range, which most likely contribute to the decrease in aerobic swimming capabilities at higher temperatures.     

The role of nest surface temperatures and the brain in influencing ant metabolic rates

Thermal limits of insects can be influenced by recent thermal history: here we used thermolimit respirometry to determine metabolic rate responses and thermal limits of the dominant meat ant, Iridomyrmex purpureus. Firstly, we tested the hypothesis that nest surface temperatures have a pervasive influence on thermal limits. Metabolic rates and activity of freshly field collected individuals were measured continuously while ramping temperatures from 44 °C to 62 °C at 0.25 °C/minute. At all the stages of thermolimit respirometry, metabolic rates were independent of nest surface temperatures, and CT_max did not differ between ants collected from nest with different surface temperatures. Secondly, we tested the effect of brain control on upper thermal limits of meat ants via ant decapitation experiments (‘headedness’). Decapitated ants exhibited similar upper critical temperature (CT_max) results to living ants (Decapitated 50.3±1.2 °C: Living 50.1±1.8 °C). Throughout the temperature ramping process, ‘headedness’ had a significant effect on metabolic rate in total (Decapitated V̇CO₂ 140±30 µl CO₂ mg⁻¹ min⁻¹: Living V̇CO₂ 250±50 CO₂ mg⁻¹ min⁻¹), as well as at temperatures below and above CT_max. At high temperatures (>44 °C) pre- CT_max the relationships between I. purpureus CT_max values and mass specific metabolic rates for living ants exhibited a negative slope whilst decapitated ants exhibited a positive slope. The decapitated ants also had a significantly higher Q₁₀:25–35 °C when compared to living ants (1.91±0.43 vs. 1.29±0.35). Our findings suggest that physiological responses of ants may be able to cope with increasing surface temperatures, as shown by metabolic rates across the thermolimit continuum, making them physiologically resilient to a rapidly changing climate. We also demonstrate that the brain plays a role in respiration, but critical thermal limits are independent of respiration levels.     

Temperature and immobility reaction in Rana temporaria

Experiments were conducted on two groups of Rana temporaria acclimatized to 7°C and to 14°C. Two hours prior to the experiments the animals were divided into six groups of 40 subjects each and placed in containers at temperatures of 5°, 10°, 15°, 20°, 25° and 30°C. Frogs remained immobile for a shorter time in temperatures which differed little from those of acclimatization. It was concluded that the body temperature interferes with the duration of the immobility reaction.     

Seasonal acclimation in resting metabolism of the skink, Mabuya brevicollis (Reptilia: Scincidae) from southwestern Saudi Arabia

The resting metabolic rate (RMR) of seasonally-acclimated Mabuya brevicollis of various body masses was determined at 20, 25, 30, 35 and 40 °C, using open-flow respirometry. RMR (ml g⁻¹ h⁻¹) decreased with increasing mass at each temperature. RMRs increaProd. Type: FTPsed as temperature increased. The highest and lowest Q₁₀ values were obtained for the temperature ranges 20–25 °C and 30–35 °C for the summer-acclimated lizards. The exponent of mass “b” in the metabolism-body mass relation ranged from 0.41 to 0.61. b values were lower in the autumn and winter-acclimated lizards than in spring and summer-acclimated lizards. Seasonal acclimation effects were evident at all temperatures (20–40 °C) for M. brevicollis. Winter-acclimated skinks had the lowest metabolic rates at different temperatures. The pattern of acclimation exhibited by M. brevicollis may represent a useful adaptation for lizards inhabiting subtropical deserts to promote activity during their active seasons.     

Seasonal variations in basal metabolic rate, lower critical temperature and responses to temporary starvation in the arctic fox (Alopex lagopus) from Svalbard

Metabolic rates of four resting, post-absorptive male adult summer- and winter-adapted captive arctic foxes (Alopex lagopus) were recorded. Basal metabolic rates (BMR) varied seasonally with a 36% increase from winter to summer, while body mass was reduced by 17% in the same period. The lower critical temperature (T _1c) of the winter-adapted arctic fox was estimated to −7°C, whereas T _lc during summer was 5°C. The similarity of these values, which are much higher than hitherto assumed (e.g. Scholander et al. 1950b), is mainly due to a significantly (P<0.05) lower BMR in winter than in summer. Body core (stomach) temperature was stable, even at ambient temperatures as low as −45°C, but showed a significant (P<0.05) seasonal variation, being lower in winter (39.3±0.33°C) than in summer (39.8±0.16°C). The thermal conductivity of arctic fox fur was the same during both seasons, whereas the thermal conductance in winter was lower than in summer. This was reflected in an increase in fur thickness of 140% from summer to winter, and in a reduced metabolic response to ambient temperatures below T _lc in winter. Another four arctic foxes were exposed to three periods of forced starvation, each lasting 8 days during winter, when body mass is in decline. No significant reduction in mass specific BMR was observed during the exposure to starvation, and respiratory quotient was unchanged at 0.73±0.02 during the first 5 days, but dropped significantly (P<0.05) to 0.69±0.03 at day 7. Locomotor activity and body core (intraperitoneal) temperature was unaltered throughout the starvation period, but body mass was reduced by 18.5±2.1% during these periods. Upon re-feeding, locomotor activity was significantly (P<0.05) reduced for about 6 days. Energy intake was almost doubled, but stabilised at normal levels after 11 days. Body mass increased, but not to the level before the starvation episodes. Instead, body mass increased until it reached the reduced body mass of ad libitum fed control animals. This indicates that body mass in the arctic fox is regulated according to a seasonally changing set point.