Temperature and the tropical tortoise Kinixys spekii: constraints on activity level and body temperature

Movements of five Kinixys spekii were measured continuously during six weeks of their activity season, by thread-trailing. The mean daily movement distance was negatively correlated with maximum shade air temperature, but not significantly related to minimum temperature, rainfall, or humidity. There was a midday period of inactivity of increasing length as maximum air temperature exceeded 29° C. Temperatures of models suggest that lower activity on hot days was due to the risk of overheating in this small (mean mass 617 g) tortoise. Kinixys spekii had a mean field body temperature (T^b) of 27° C, which is low compared to other tortoises (including sympatric Geochelone pardulis, mean T^b= 32.5° C), but salivated at a similar T^b (38.4° C). This pattern also occurs in other small species; mean and maximum field T^bs of tortoises are positively correlated with body mass, but salivation and critical maximum T_bs do not vary with body mass. Low field T_b provides a wide safety margin before evaporation of water becomes necessary. Kinixys sprkii had a short annual activity period, with about 95% of sightings in four months (December to March). Monthly sightings of K. spekii were correlated with rainfall, but not significantly related to temperature or humidity. Seasonal activity is therefore related to rainfall, but within the rainy season the level and pattern of daily activity is related to temperature.     

Prolonged and daily torpor in the feathertail glider, Acrobates pygmaeus (Marsupialia: Acrobatidae)

Deep and prolonged torpor in marsupials is only known from the pygmy possums, family Burramyidae. We investigated the pattern of torpor in the feathertail glider Acrobates pygmaeus (Acrobatidae) to determine whether members of other marsupial families also possess the ability of remaining torpid for several days with body temperatures (T_b) approaching 0°C. At high air temperatures (T_a) of 15 and 20°C, A. pygmaeus usually exhibited daily torpor. Torpor bouts at T_a 12°C usually lasted for about 2˙5 days and at T_a 8°C up to 5˙5 days. The metabolic rate during torpor was reduced to about 1% of that in normothermic, resting individuals. The T_b during torpor was regulated at about 2°C when T_a fell below about 0˙8 °C. Arousal from torpor was rapid and the mean fastest rewarming rate was 0˙88°C/min. While A. pygmaeus exhibited deep and prolonged torpor, its pattern differed somewhat from deep hibernation. Acrobates pygmaeus did not show prehibernation fattening and a subsequent prolonged hibernation period and it appears that prolonged torpor is used only in emergency situations.     

Temperature and the tropical tortoise Kinixys spekii: tests of thermoregulation

The mean body temperature (T_b) of active Kinixys spekii did not vary with sex or type of activity, or between hot days (maximum ambient temperature T_a > 29°C) and cool days. On hot days, T_b increased rapidly in the morning, and was constant during the late afternoon after midday inactivity. On cool days, T_b increased more slowly in the morning, and decreased during the afternoon. The slopes of T_b on T_a overall, and on hot days, were close to one, suggesting that tortoises were thermoconformers; the slope was greater than one on cool days. In a second test of thermoregulation, T_bs were compared with temperatures of null models (T_m). Tortoises were clearly thermoregulators compared to 'active-all-day' models. 'Activity-time' models had T_m more similar to T_b. Nevertheless, detailed comparison showed that tortoises were thermoregulating in the late morning, and that this was by choice of microenvironment, rather than ceasing activity when T_b reached a high level. These results are discussed in relation to E, a measure of the effectiveness of thermoregulation based on comparison of T_b and T_m with the set point range (T_set) selected in a thermal gradient. A set of three indices, which separate the variability of T_b, the difference between T_b and T_m, and between T_b and T_set, is suggested as a more generally applicable summary of thermoregulation in ectotherms.     

Thermoregulation, energy metabolism, and torpor in blossom-bats, Syconycteris australis (Megachiroptera)

Since little information is available on torpor in bats of the suborder Megachiroptera, we investigated whether the small (18 g) blossom-bat Syconycteris australis displays torpor in the laboratory. Bats entered daily torpor when food and water were withheld for one night and the air temperature (T_a) was below about 26°. Torpor began shortly after lights went on in the morning and lasted for a maximum of 12 hours. During torpor at T_a18°, metabolic rates fell to a minimum of about 15% of that in resting individuals at the same T_a, and to about 40% of the basal metabolic rate. The body temperature (T_b) during torpor was metabolically defended at or above about T_b 18°. Individuals that did not enter torpor in the morning reduced their T_b from about 34.5°, observed in resting individuals that had been fed during the previous night, to values between 30.2 and 32.8°, and the resting metabolic rate fell by about 25%. The ability to undergo short periods of torpor may explain why the distribution range of S. australis extends much further south than that of other small Australian megachiropteran bats.     

Hypometabolism in torpid goldsinny wrasse subjected to rapid reductions in seawater temperature

Goldsinny Ctenolabrus rupestris were subjected to rapid, environmentally realistic, reductions in temperature at 2° C increments from 10 to 4° C over a 3-day period in full-strength sea water. In separate experiments, oxygen uptake measurements and ultrasound recordings of heart rate and opercular motion were carried out at regular intervals over the same temperature regime. Mean oxygen uptake rates fell from 0.042 to 0.028 ml O₂ g⁻¹ h⁻¹ between 10 and 6° C respectively (Q₁₀=2.71). Between 6 and 4° C mean rates decreased from 0.028 to 0.008 ml O₂ g⁻¹ h⁻¹ (Q₁₀=542). Mean opercular motion and heart beat rates decreased from 49.5 and 60.3 beats min⁻¹ respectively at 10° C to 18.7 and 18.0 beats min⁻¹ respectively at 4° C. Most goldsinny subjected to 4° C were observed in a torpid state and would not react to external stimulation. Opercular motion was erratic at 4° C and would at times cease altogether for periods up to 1.3 min duration. Heart movement was diffcult to detect at 4° C and may also have ceased for prolonged periods. Q₁₀ values for opercular motion and heart beat rates recorded between 6 and 4° C were 6.39 and 24.52 respectively compared with values of 2.42 and 2.93 respectively recorded between 10 and 8° C. Such large depressions in metabolism appear not to have been reported previously for a marine fish species. No goldsinny mortalities were recorded at any temperature. The possibility that hypometabolic torpor is an adaptive strategy for goldsinny survival at low environmental temperatures is discussed.     

The effects of acute temperature change on cost of transport at maximal labriform speed in bluegill Lepomis macrochirus

The effects of acute temperature change on the cost of bluegill Lepomis macrochirus swimming were quantified. At 14° C, maximum labriform swimming speed ( U _lab,max) was reduced relative to that at the acclimation temperature of 22° C, but total cost of transport ( T _TC) remained unchanged. At 30° C, U _lab,max was the same as at 22° C, but T _TC was 66% greater.     

The utilization of patchy thermal microhabitats by the ectothermic insect predator, Cicindela sexguttata

Abstract. 1. Tiger beetles ( Cicindela ) of open habitats have served as model ectotherms in studies of the dependence of activity and habitat utilization on temperature. Potential departures from the cicindelid model were investigated in Cicindela sexguttata , a species inhabiting forests where thermal resources are patchy and ephemeral.
2. Body temperatures (T_b) were determined by inserting thermocouples into beetles immediately after observing specific behaviours in the field. Cicindela sexguttata elevated T_b by basking, foraged at a preferred T_b of 32.8 °C, and stilted, sun-faced, or sought shade when T_b exceeded 35 °C. Although these behaviours were typical of Cicindela , their set points were lower than those of species in more open habitats.
3. Illuminated substrates were utilized for basking and foraging. Beetles were dispersed throughout the forest floor in early spring, but became aggregated in light gaps when the canopy leafed out. Operative temperatures of thermal models indicated that beetles were unable to maintain the preferred T_b in shade and would not be able to maintain a preferred T_b in light gaps during the autumn, when adults are normally in diapause.
4. Beetles were confined to foraging in light gaps once the canopy was closed. Foraging rate and searching speed were independent of T_b, in contrast to other cicindelids. Adults rarely searched for prey, but ambushed small arthropods that alighted in the light gap. Dependence on patches of illumination as thermal resources may increase prey capture, intraspecific encounters, and risk of predation, and preclude foraging in the autumn when Cicindela species of open habitats are also active.     

Alterations to the swimming performance of carp, Cyprinus carpio, as a result of temperature acclimation

Groups of common carp were acclimated to either 10°C or 28°C for 6 weeks. Fish were then exercised at 10°C or 20°C, and the critical swimming speed (fatigue velocity) was measured. At 10°C, cold-acclimated carp were capable of significantly higher swimming speeds. When exercised at 20°C. however, the situation was reversed, and warm-acclimated carp exhibited improved swimming ability. These results provide direct evidence that acclimation of the contractile proteins is beneficial across a wide temperature range. Following acclimation to low environmental temperatures the critical swimming speed exhibited a Q₁₀ of only 1.1 for the temperature range 10–20°C. compared to a value of 2.9 for fish acclimated to the higher temperature.     

Effect of temperature on swimming performance of sea bass juveniles

At four temperatures ( T= 15, 20, 25 and 28° C) swimming performance of Dicentrarchus labrax was significantly correlated with total length (23–43 mm L _T); r²=0.623–0.829). The relative critical swimming speed ( RU _crit= U _crit L _T⁻¹), where U _crit is the critical swimming speed, was constant throughout the L _T range studied. The significant effect of temperature on the relative critical swimming speed was described binomially: RU _crit=−0.0323T²+ 1.578 T −10.588 (r²=1). The estimated maximum RU _crit (8.69 L _T s⁻¹) was achieved at 24.4° C, and the 90% performance level was estimated between 19.3 and 29.6° C.     

Effects on temperature on spontaneous and thyroxine-stimulated locomotor activity of Atlantic cod

Spontaneous locomotor activity of cod Gadus morhua maintained at 6° C tripled from February to May. In contrast, locomotor activity of cod held at 2° C was significantly lower than at 6° C (between 25 and 65% lower) and the seasonal increase was smaller. Plasma levels of both thyroxine (T₄) and triiodothyronine (T₃) did not differ between 2 and 6° C. T₄ injection increased locomotor activity by 10% for both temperature regimes. These data indicate that low water temperature reduces locomotor activity associated with migration in cod and that thyroid hormones are not involved in this decrease. This study provides a possible mechanism through which cold waters may affects migration and distribution of cod via its Effects on locomotor activity and swimming speed.     

Temperature effects on metabolic rate, swimming performance and condition of Pacific cod Gadus macrocephalus Tilesius

Critical swimming speed ( U _crit) and rate of oxygen consumption of Pacific cod Gadus macrocephalus acclimated to 4 and 11° C were determined to assess the influence of water temperature on performance. The physiological effect of exercise trials on fish held at two temperatures was also assessed by comparing haematocrit and plasma concentrations of cortisol, metabolites and ions collected from fish before and after testing. The U _crit of fish acclimated and exercised at 4° C did not differ from those acclimated and exercised at 11° C [1·07 body lengths (total length) s⁻¹]. While the standard metabolic rate of 11° C acclimated fish was 28% higher than that of 4° C fish, no significant difference was observed between fish acclimated at the two temperatures. Plasma concentrations of cortisol, glucose and lactate increased significantly from pre- to post-swim in both groups, yet only concentrations of cortisol differed significantly between temperature treatments. Higher concentrations of cortisol in association with greater osmoregulatory disturbance in animals acclimated at the lower temperature indicate that the lower water temperature acted as an environmental stressor. Lack of significant differences in U _crit between temperature treatments, however, suggests that Pacific cod have robust physiological resilience with respect to swimming performance within temperature changes from 4 to 11° C.     

The effects of temperature and water concentration on the otolith incorporation of barium and manganese in black rockfish Sebastes melanops

Observations of multiple years of geographic variation in [Ba:Ca]_otolith and [Mn:Ca]_otolith in black rockfish Sebastes melanops prompted this study to examine the effects of temperature and water concentration on the otolith incorporation of Ba and Mn in this wholly marine species. The replicated experiment design consisted of two water temperatures (7·4 and 13·0° C) and four water concentrations of Ba:Ca and Mn:Ca. A positive, linear relationship between [Ba:Ca]_water and [Ba:Ca]_otolith was observed at both temperatures. A positive temperature effect was also observed with mean partition coefficients for Ba ( D _Ba) greater in the 13° C than in the 7·4° C treatments (mean = 0·061 and 0·048, respectively). There was no relationship between [Mn:Ca]_water and [Mn:Ca]_otolith although a negative temperature effect was observed. Mean partition coefficients for Mn ( D _Mn) were lower in the 13° C than in the 7·4° C treatments (mean = 0·027 and 0·036, respectively). The data presented support the assumption of a positive, linear relationship between water and otolith Metal:Ca concentrations for Ba:Ca but not for Mn:Ca. Thus, although indicative of residence in distinct water masses, observed variation in [Metal:Ca]_otolith may not reflect variation in water concentration and can be affected by temperature. Caution should be applied in the interpretation of geographic variation of [Mn:Ca]_otolith until the mechanisms regulating its incorporation are more fully understood.     

The influence of thermal parameters on the acclimation responses of pinfish Lagodon rhomboides exposed to static and decreasing low temperatures

Pinfish Lagodon rhomboides acclimation rates were determined by modelling changes in critical thermal minimum ( T _{crit min}, ° C) estimates at set intervals following a temperature decrease of 3–4° C. The results showed that pinfish gained a total of 3·7° C of cold tolerance over a range of acclimation temperatures ( T _acc, ° C) from (23–12° C), that cold tolerance increased with exposure time to the reduced temperature at all T _acc, but that the rate of cold tolerance accruement (mean 0·14° C day⁻¹) was independent of T _acc. A highly significant ( P < 0·001) multivariate predictive model was generated that described the acclimation rates and thermal tolerance of pinfish exposed to reduction in water temperature: log₁₀ T _{crit min}= 0·41597 − 0·01704 T _acc+ 0·04320 T _plunge− 0·08376[log₁₀ ( t + 1)], where T _plunge is plunge temperature (° C) and t is the time (days). A comparison of the present data, with acclimation rate data for other species, suggests that factors such as latitude or geographic range may play a more important role than ambient temperature in determining cold acclimation rates in fishes.     

The effect of temperature and acclimation period on repeat swimming performance in cutthroat trout

Hatchery cutthroat trout Oncorhynchus clarki clarki were used to examine the effects of 48 h and 3 week temperature acclimation periods on critical swimming speed ( U _crit). The U _crit was determined for fish at acclimation temperatures of 7, 14 and 18° C using two consecutive ramp‐ U _crit tests in mobile Brett‐type swim tunnels. An additional group was tested at the stock's ambient rearing temperature of 10° C. The length of the temperature acclimation period had no significant effect on either the first or the second U _crit( U _crit‐1 and U _crit‐2, respectively) or on the recovery ratio (the quotient of U _crit‐2  U _crit‐1⁻¹). As anticipated, there was a significant positive relationship between U _crit‐1 and temperature ( P  < 0·01) for both acclimation periods, and an increasing, though non‐significant, trend between U _crit‐2 and temperature ( P  = 0·10). Acclimation temperature had no significant effect ( P  = 0·71) on the recovery ratio. These results indicate that a 48 h acclimation to experimental temperatures within the range of −3 to +8° C of the acclimation temperature may be sufficient in studies of swimming performance with this species. This ability to acclimate rapidly is probably adaptive for cutthroat trout and other species that occupy thermally variable environments.     

Ventilatory mechanisms and the effect of hypoxia and temperature on the embryonic lesser spotted dogfish

Small, intermediate and large-sized embryos of the dogfish Scyliorhinus canicula utilize different ventilatory methods; small and intermediate embryos rely on body movement alone to stir either the jelly or sea water in the capsule, large embryos use conventional pharyngeal pumping to pump water through the case. The effects of environmental changes in O₂ tension (0.5–100% air saturation) and temperature (6–18°C) upon ventilatory mechanisms in the developing embryo in situ were studied using non-invasive ultrasonography. All three embryo classes increased ventilation rate with rising temperature: for small embryos, y=2.02x+3.295 ( P <0.01); for intermediate embryos, y=3.51x+0.395 ( P <0.01); and for large embryos, y=3.81x+9.39 ( P <0.01); where y=ventilatory frequency (tail beats min⁻¹ or pump cycles min⁻¹) and x=temperature (°C). Q ₁₀ (6–16°C)=5.0, 2.45, and 2.08 for small, intermediate and large embryos, respectively; corresponding Q ₁₀ (8–18°C) values were 2.09, 2.62, and 2.02. It is suggested that the extreme response of small embryos to 6°C is related to a different state of development in either chemoreceptors or muscle blocks. There was no significant change in ventilatory frequency induced by chronic (2 h) hypoxia. Dogfish embryos are oxyconformers at 8°C but oxyregulators at higher temperatures. Water flow through an eggcase occupied by a large embryo was studied also. Water enters the open eggcase of a large embryo, drawn in by the buccal/opercular pump of the respiring embryo, via holes at the posterior end of the eggcase. Expired water exits holes at the anterior end of the eggcase. The mean residence time for water in the case is 50 s at 8°C, giving a transit velocity of 1.36 mm s⁻¹.     

Acclimation is beneficial at extreme test temperatures in the Danube crested newt, Triturus dobrogicus (Caudata, Salamandridae)

Despite many studies demonstrating the effect of acclimation on behavioural or physiological traits, considerable debate still exists about the evolutionary significance of this phenomenon. One of the unresolved issues is whether acclimation to warmer temperature is beneficial at treatment or at more extreme test temperatures. To answer this question, we assessed the effect of thermal acclimation on preferred body temperatures ( T _ps), maximum swimming and running speed, and critical thermal maximum ( CT _max) in the Danube crested newt ( Triturus dobrogicus ). Adult newts were kept at 15 °C (control) and 25 °C (treatment) for 8 weeks prior to measurements. We measured T _ps in an aquatic thermal gradient over 24 h, maximum speeds in a linear racetrack at six temperatures (5–33 °C), and CT _max in a continuously heated water bath. T _ps were higher in newts kept at 15 °C than in those kept at 25 °C. The maximum swimming speed did not acclimate. The maximum running speed at 30–33 °C was substantially higher in newts kept at 25 °C than in those kept at 15 °C. CT _max increased with the treatment temperature. Hence, we conclude that the acclimation response to warm temperature is beneficial not at treatment but at more extreme temperatures in newts.  © 2007 The Linnean Society of London, Biological Journal of the Linnean Society , 2007, 90 , 627–636.     

Temperature-induced changes in the locomotor capacity of juveniles of Marenzelleria viridis (Polychaeta, Spionidae)

Abstract. Populations of Marenzelleria viridis in the Chester River (Kent County, Maryland) experience temperatures ranging from over 30°C in summer to near freezing in winter. Interestingly, M. viridis swims actively in winter. This observation led us to examine the relationship between locomotor capacity and temperature in individuals of M. viridis . Juvenile specimens were collected in February ("cold animals") and June ("warm animals"). Video analysis revealed that swimming is achieved by flexing the body in cyclic, helical waves. Wave frequencies were measured as an index of locomotor capacity at 5°C, 15°C, and 25°C. The mean wave frequencies of cold animals were 5.4 Hz at 5°C and 7.1 Hz at 15°C (Q₁₀= 1.3); the mean wave frequencies of warm animals were 6.1 Hz at 15°C and 7.8 Hz at 25°C (Q₁₀= 1.3). The effects of changes in water viscosity on wave frequency between 5–25°C were not significant. These results demonstrate that the temperature sensitivity of locomotor capacity in juvenile M. viridis is quite low. We conclude that low temperature sensitivity enables M. viridis to be active throughout the year.     

Endurance at intermediate swimming speeds of Atlantic mackerel, Scomber scombrus L., herring, Clupea harengus L., and saithe, Pollachius virens L.

Endurance and swimming speed were measured in mackerel, herring and saithe when they were induced by the optomotor response to swim at prolonged speeds along a 28-m circular track through still water in a 10-m diameter gantry tank. The maximum sustained swimming speed ( U _ms was measured as body lengths per second ( b.l.s ⁻¹) for each species and for saithe of different size groups. Herring with U _ms of 4.06 b.l.s ⁻¹ (25.3 cm, 13.5°C) were the fastest, mackerel U _ms was 3.5 b.l.s ¹ (33 cm, 11.7°C) and saithe (14.4°C) showed a size effect where U _ms at 25 cm was 3.5 b.l.s ¹ and at 50 cm 2.2 b.l.s ¹. When swimming at speeds higher that U _ms, all three species showed reduced endurance as speed increased. How the curved track reduces the swimming speed is discussed.     

Effects of temperature, hypoxia and activity on the metabolism of juvenile Atlantic cod

Standard metabolic rate (SMR), active metabolic rate (AMR) and critical oxygen saturation ( S_crit ) were measured in Atlantic cod Gadus morhua at 5, 10 and 15° C. The SMR was 35.5, 57.0 and 78.2 mg O₂ kg⁻¹ h⁻¹ and S_crit was 16.5, 23.2 and 30.3%, at 5, 10 and 15° C, respectively. Previously reported SMR for Atlantic cod from arctic waters at 4° C was twice that measured at 5° C in the present study. A possible intraspecific latitudinal difference in the SMR is discussed. The AMR was 146.6, 197.9 and 200.4 mg O₂ kg⁻¹ h⁻¹ and the critical swimming speed ( U_crit ) was 1 6, 1.7 and 1.9 at 5, 10 and 15° C, respectively. The maximum oxygen consumption was found to be associated with exercise, rather than recovery from exercise as previously reported in another Study of Cod metabolism.     

Influence of temperature on life-table parameters of Stethorus gilvifrons (Mulsant) (Coleoptera: Coccinellidae) fed on Tetranychus urticae Koch

The influence of temperature on life-table parameters, fecundity and survivorship of the predatory ladybird, Stethorus gilvifrons , fed on Tetranychus urticae was determined at seven constant temperatures of 15°C, 20°C, 25°C, 28°C, 30°C, 35°C and 40°C. No development was observed at 40°C, thus being regarded as the threshold for the development of S. gilvifrons . The results indicate a significant decrease in male and female longevity with increasing temperature from 15°C to 35°C. The longest and shortest longevity were 18.40 and 12.75 days for males and 17.40 and 8.80 days for females, respectively. The intrinsic rate of natural increase ( r _m ) and the net reproductive rate ( R ₀) of S. gilvifrons linearly increased with increasing temperatures from 15°C to 35°C, while the mean generation time ( T ) and doubling time (DT) decreased linearly within this temperature range. The highest values of r _m (0.240 females/female/day) and R ₀ (59.27 females/female) and the lowest mean generation time (17.01 days) and DT (2.88 days) were recorded at 35°C. The maximum (185.50 eggs) and minimum (25.50 eggs) measurement of total fecundity was also recorded at 35°C and 15°C, respectively. The results indicate that temperature greatly affected fecundity, survivorship and life-table parameters of S. gilvifrons , and that 35°C is a suitable temperature for population growth of this predator.