Temperature regulation in a burrow-nesting tropical seabird,the Wedge-tailed Shearwater (Puffinus pacificus)

Summary At low air temperatures (2.3–13.9°C), Wedge-tailed Shearwaters (Puffinus pacificus) shivered and their oxygen consumption increased to as much as 283% of the mean value (0.77 ml O₂/g·h) within the thermoneutral zone of air temperature (23–34°C). The minimal thermal conductance of the tissues and plumage was similar to the value predicted from the body mass (320.5 g). The oxygen consumption of the birds within their thermoneutral zone was lower than predictions based on body mass. At elevated air temperatures, the shearwaters panted at respiratory frequencies as high as 260 respirations/min; maximal respiratory frequencies were not invoked until the birds had become hyperthermic. During exposure to a hot environment, the oxygen consumption of the birds increased and in most instances the shearwaters were not able to lose heat equivalent to their concurrent metabolic heat production.Symbols and abbreviations BMR basal metabolic rate - C _total total thermal conductance - f respiratory frequency - TEWL total evaporative water loss - T _st stomach temperature - T _re rectal temperature     

Physiological significance of behavioral hypothermia in hypoglycemic frogs (Rana catesbeiana)

Hypoxia elicits a number of compensatory responses in animals, including behavioral hypothermia. The hypothesis that hypoglycemia induces hypothermia in the bullfrog Rana catesbeiana was tested and that this behavioral response would be beneficial. Frogs equipped with a temperature probe were tested in a thermal gradient (10–40°C). Insulin (15 IU kg⁻¹) caused significant reduction of body temperature, from 25.0 to 17.8°C. A non-metabolizable glucose analogue, 2-deoxy-d-glucose (2-DG, 50 mg kg⁻¹),which blocks intracellular glucose utilization, was also injected and caused a similar drop in body temperature, despite an increase in plasma glucose levels. To assess the possible benefits of hypoglycemia-induced hypothermia, the effects of insulin and 2-DG injections were measured on plasma glucose concentration and on oxygen consumption of frogs equilibrated at 10, 20 and 30°C. The plasma glucose was elevated at higher temperatures and so was oxygen consumption. The insulin caused a significant reduction of plasma glucose concentration (about 1.22 μMol ml⁻¹) whereas 2-DG caused a significant increase (about 0.70 μMol ml⁻¹) at 30°C. Both drugs caused a reduction of oxygen consumption (approximately 0.388 and 0.382 ml min⁻¹ kg at 30°C after insulin and 2-DG injection, respectively). No effect of either insulin or 2-DG was observed when the animals were equilibrated at 10°C. In conclusion, hypothermia may be a beneficial response to hypoglycemia in frogs.     

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     

Oxygen consumption rates of adults and chicks during brooding in king quail (Coturnix chinensis)

Oxygen consumption rates were measured in chicks (0–7 days of age), and in non-brooding and brooding adults. Brooded chicks maintained a constant oxygen consumption rate at a chamber ambient temperature of 10–35°C (0–5 days of age: 2.95ml O₂·g^-1·h^-1 and 6–17 days of age: 5.80 ml O₂·g^-1·h^-1) while unbrooded chicks increased oxygen consumption rate at ambient temperature below 30°C to double the brooded oxygen consumption rate at 25 and 15°C for chicks < 5 days of age and>5 days of age, respectively. The massspecific oxygen consumption rate of breeding male and females (non-brooding) were significantly elevated within the thermoneutral zone thermal neutral zone (28–35°C) in comparison to non-breeding adults. Below the thermal neutral zone, oxygen consumption rate was not significantly different. The elevation in oxygen consumption rate of breeding quail was not correlated with the presence of broodpatches, which developed only in females, but is a seasonal adjustment in metabolism. Male and females that actively brooded one to five chicks had significantly higher oxygen consumption rate than non-brooding quail at ambient temperature below 30°C. Brooding oxygen consumption rate was constant during day and night, indicating a temporary suppression of the circadian rhythm of metabolism. Brooding oxygen consumption rate increased significantly with brood number, but neither adult body mass nor adult sex were significant factors in the relationship between brooding oxygen consumption rate and ambient temperature. The proportion of daylight hours that chicks were brooded by parents was negatively correlated with ambient temperature. After chicks were 5 days old brooding time was reduced but brooding oxygen consumption rate was unchanged. Heat from the brooding parent appeared to originate mainly from the apteria under the wings and legs rather than the broodpatch. The parental heat contribution to chick temperature regulation below the chicks' thermal neutral zone is achieved by increasing parental thermal conductance by a feedback control similar to that suggested for the control of egg temperature via the brood-patch. It is concluded that the brooding period is an energetic burden to parent quail, and the magnitude of the cost increases directly with brood number and inversely with ambient temperature during this period. The oxygen consumption rate of brooding parents was 5.80–6.90 ml O₂·g^-1·h^-1 (ambient temperature 10–15°C) at night and up to 5.10 ml O₂·g^-1·h^-1 (ambient temperature 18°C) during the day, which are 100 and 40% higher than non-brooding birds, respectively.Abbreviations bm body mass - SMR standard metabolic rate - T _a ambient temperature - T _b body temperature - I/O₂ oxygen consumption rate - C _wet wet thermal conductance - TNZ thermal neutral zone - ANOVA analysis of variance - ANCOVA analysis of covariance     

The emergence of endothermy in the black-footed and Laysan albatrosses

Eggs with pip-holes of the black-footed (Diomedea nigripes) and Laysan (Diomedea immutabilis) albatrosses were exposed to various air temperatures in the range 20–35°C in order to detect signs of incipient endothermy in late embryos. No evidence of endothermy was found. In contrast, the O₂ consumption of most hatchlings increased in response to cooling, the O₂ consumption at an air temperature of 25° C exceeding that between 34 and 35°C by 40%. In a minority of hatchlings this response was not seen. It was suggested that endothermy may develop at some time during the 24 h after hatching.Abbreviations bm body mass - C _total total thermal conductance of tissues and plumage - f respiratory frequency - FE_{O 2} fractional concentration of oxygen in air leaving chamber - FI_{O 2} fractional concentration of oxygen in air entering chamber - T _a an temperature - T _b deep-body temperature - V air-flow rate - VO₂ oxygen consumption     

Seasonal changes in daily metabolic patterns of Lacerta viridis

Summary Lacerta viridis maintained under natural photoperiodic conditions show daily and seasonal changes in metabolic rates and body temperature (T _b) as well as seasonal differences in sensitivity to temperature change. At all times of the year lizards have a daily fluctuation in oxygen consumption, with higher metabolic rates during the light phase of the day when tested at a constant ambient temperature (T _a) of 30°C. Rhythmicity of metabolic rate persists under constant darkness, but there is a decrease in the amplitude of the rhythm.Oxygen consumption measured at various T_as shows significant seasonal differences at T _as above 20°C. Expressed as the Arrhenius activation energy, metabolic sensitivity of Lacerta viridis shows temperature dependence in autumn, which changes to metabolic temperature independence in spring at T _as above 20°C. The results indicate a synergic relationship between changing photoperiod and body temperature selection, resulting in seasonal metabolic adjustment and seasonal adaptation.Abbreviations ANOVA analysis of variance - LD long day (16 h light) - SD short day (8 h light) - T _a ambient temperature - T _b body temperature     

Oxygen consumption of a Chaoborus species from a neotropical reservoir (socuy reservoir,Venezuela)

Oxygen consumption of all four larval instars of a Chaoborus species from Socuy Reservoir in western Venezuela was studied under laboratory conditions at 25°C. On a logarithmic basis, oxygen consumption per organism increased as a smooth, linear function of body weight (0.49 power of body weight). Observed rates were lower than other Chaoborus species with comparable body weight at the same temperature. Oxygen consumption per unit weight decreased from smaller to large instar larvae. With the exception of instar I, values of oxygen consumption per unit weight were lower than values reported for other Chaoborus species. The results suggest that our species have low energy demands for maintenance, and are consistent with suggestions about high efficiency in use of energy in genus Chaoborus.     

Heterothermy in elephant shrews, Elephantulus spp. (Macroscelidea): daily torpor or hibernation?

The physiological parameters of heterothermy (e.g. minimum body temperature and oxygen consumption, percentage metabolic reduction, and bout length) were measured in two species of Elephantulus elephant shrews (Elephantulus myurus and Elephantulus rozeti; Macroscelidea) as a function of ambient temperature. Both species displayed deep torpor whereby the body temperatures of ca. 5 °C and oxygen consumption as low as 2% of basal metabolic rate were attained. Torpor bout length (n=57 bouts) never exceeded 24 h. These data are characteristic of both hibernation (minimum body temperature and metabolism) and daily torpor (bout length), and argue that these two physiological responses may not necessarily have separate evolutionary origins. Accepted: 26 July 2000     

Oxygen consumption by the bivalve Donax vittatus (da Costa)

The acute oxygen consumption of Donax vittatus (da Costa) freshly collected at different times from a beach at Barrassie, Ayrshire, Scotland, has been measured at different temperatures. The logarithmic relationship between oxygen consumption and body weight showed a significant difference on only one occasion, and a common regression coefficient (b) of 0.865 could be used for regressions of oxygen consumption on weight. Over the temperature range 2.9–20 °C oxygen consumption rose with temperature. There was a linear decline of Q₁₀ with temperature in the range 2.9 –20 °C. Differences in values of the constant (a) in the regression equation suggest that there is some acclimation to temperature, resulting in rotation of the rate/temperature curve counterclockwise for warm-acclimated animals, and a reduction of Q₁₀ in cold-acclimated animals. The differences in oxygen consumption which result are small and appear to have little practical significance. High levels of metabolically-inactive materials such as stored glycogen reserves lead to a reduction in the weight-specific oxygen consumption. Spawning animals show an increased oxygen consumption.     

Distribution, Habitat Correlates, and Conservation of Loris lydekkerianus in Karnataka, India

We surveyed slender lorises (Loris lydekkerianus) in Karnataka, south India intermittently during November 2001–July 2004 and estimated their relative abundance via direct sightings. Two subspecies, Loris lydekkerianus lydekkerianus and L. l. malabaricus, with different morphological traits, occur in the eastern drier region and the western wet region of the state, respectively. The distribution of Loris lydekkerianus lydekkerianus is patchy in a small region in the southeast, which contradicts earlier reports of its abundance throughout the state. Loris lydekkerianus malabaricus occurs throughout the Western Ghats as a contiguous population. The encounter rates of Loris lydekkerianus lydekkerianus and L. l. malabaricus are 0.41 individuals/km and 0.21 individuals/km, respectively. Whereas several forest tracts in the distributional range of Loris lydekkerianus malabaricus are protected areas, no such area exists in the distributional range of L. l. lydekkerianus. Loris lydekkerianus faces serious challenges of conservation because it largely occurs in commercial plantations, which can be relatively unstable habitats as harvesting can take place at any time.

The combined effect of body size and temperature on oxygen consumption rates and the size-dependency of preferred temperature in European perch Perca fluviatilis

The present study determined the effect of body mass and acclimation temperature (15–28°C) on oxygen consumption rate (ṀO₂) and the size dependency of preferred temperature in European perch Perca fluviatilis. Standard metabolic rate (SMR) scaled allometrically with body mass by an exponent of 0.86, and temperature influenced SMR with a Q₁₀ of 1.9 regardless of size. Maximum metabolic rate (MMR) and aerobic scope (MMR-SMR) scaled allometrically with body mass by exponents of 0.75–0.88. The mass scaling exponents of MMR and aerobic scope changed with temperature and were lowest at the highest temperature. Consequently, the optimal temperature for aerobic scope decreased with increasing body mass. Notably, fish <40 g did not show a decrease aerobic scope with increasing temperature. Factorial aerobic scope (MMR × SMR⁻¹) generally decreased with increasing temperatures, was unaffected by size at the lower temperatures, and scaled negatively with body mass at the highest temperature. Similar to the optimal temperature for aerobic scope, preferred temperature declined with increasing body mass, unaffectedly by acclimation temperature. The present study indicates a limitation in the capacity for oxygen uptake in larger fish at high temperatures. A constraint in oxygen uptake at high temperature may restrict the growth of larger fish with environmental warming, at least if food availability is not limited. Furthermore, behavioural thermoregulation may be contributing to regional changes in the size distribution of fish in the wild caused by global warming as larger individuals will prefer colder water at higher latitudes and at larger depths than smaller conspecifics with increasing environmental temperatures.     

The functional significance of ventilation frequency,and its relationship to oxygen demand in the resting brown long-eared bat,Plecotus auritus

Summary Mean oxygen consumption and simultaneous ventilation frequency of nine non-reproductive brown long-eared bats (body mass 8.53–13.33 g) were measured on 159 occasions. Ambient (chamber) temperature at which the measurements were made ranged from 10.8 to 41.1°C. Apneic ventilation occurred in 22 of the 59 measurements made when mean oxygen consumption was less than 0.5 ml·min^-1. No records of apneic ventilation were obtained when it was over 0.5 ml·min^-1. The relationship between ventilation frequency and mean oxygen consumption depended on whether ventilation was apneic or non-apneic. When ventilation was non-apneic the relationship was positive and log-linear. When ventilation was apneic the relationship was log-log. Within the thermoneutral zone ventilation frequency was not significantly different from that predicted from allometric equations for a terrestrial mammal of equivalent body mass, but was significantly greater than that predicted for a bird. A reduction in the amount of oxygen consumed per breath occurred at ambient temperatures above the upper critical temperature (39°C).Abbreviations RH relative humidity - T _a chamber temperature - vf ventilation frequency - VO₂ oxygen consumption     

Changes in body core temperatures and heat balance after an abrupt release of lower body negative pressure in humans

Changes in body core temperature (T _cor) and heat balance after an abrupt release of lower body negative pressure (LBNP) were investigated in 5 volunteers under the following conditions: (1) an ambient temperature (T _a) of 20 °C or (2) 35 °C, and (3)T _a of 25 °C with a leg skin temperature of 30°C or (4) 35°C. The leg skin temperature was controlled with water perfusion devices wound around the legs. Rectal (T _re), tympanic (T _ty) and esophageal (T _es) temperatures, skin temperatures (7 sites) and oxygen consumption were measured. The intensity of LBNP was adjusted so that the amount of blood pooled in the legs was the same under all conditions. When a thermal balance was attained during LBNP, application of LBNP was suddenly halted. The skin temperatures increased significantly after the release of LBNP under all conditions, while oxygen consumption hardly changed. The release of LBNP caused significant falls inT _cor s under conditions (1) and (3), but loweredT _cor s very slightly under conditions (2) and (4). The changes inT _es were always more rapid and greater than those ofT _ty andT _re. The falls inT _ty andT _re appeared to be explained by changes in heat balance, whereas the sharp drop ofT _es could not be explained especially during the first 8 min after the release of LBNP. The results suggest that a fall inT _cor after a release of LBNP is attributed to an increase in heat loss due to reflexive skin vasodilation and is dependent on the temperature of venous blood returning from the lower body. It is presumed thatT _es may not be an appropriate indicator forT _cor when venous return changes rapidly.     

A response-surface analysis of the relative importance of the temperature,salinity and body weight on the respiratory metabolism of the white shrimp Litopenaeus vannamei (Boone, 1931)

We used a response-surface analysis to determine the importance of different factors affecting the resting routine metabolic rate (QO₂) of the white shrimp Litopenaeus vannamei. The oxygen consumption rates were estimated using a multi-factorial design with 28 combinations of different salinities (15, 20, 25, 30, 35, 40 and 45 psu) and temperature (20, 25, 30 and 35 °C) values. The response-surface analysis produced a quadratic function showing that temperature more profoundly affects the oxygen consumption rate. Response-surface curves were generated to predict the optimal conditions resulting in oxygen consumption to better understand the successful growth of this species.     

Rates of oxygen consumption by Thais (Nucella) Lapillus (L.)

Oxygen consumption by Thais varied seasonally with higher values in summer than in winter. This seasonal difference was due in part to the effects of temperature and in part to those of feeding. During feeding, rates of oxygen consumption were high, but declined in the period between meals. There was little evidence of acclimation of oxygen consumption to changes in temperature; low (winter) rates of consumption were more sensitive to increases in temperature than were high (summer) rates. A polynomial expression, including terms for temperature and ‘time since last meal’, was derived for the constant a′ in the allometric equation relating oxygen consumption (_o2) to dry body weight: _o2 = a′.W^0.511.     

Temperature dependence of O2 consumption; opposite effects of leptin and etomoxir on respiratory quotient in mice

Objectives : The aims were to compare the temperature dependence of the metabolic rate in young ob/ob mice with that in mature ob/ob and db/db mice and to examine the effect on the metabolic substrate preference of leptin and etomoxir in ob/ob, C57BL/6J (wild‐type), and db/db mice. Research Methods and Procedures : In vivo oxygen consumption and carbon dioxide production were continuously measured by indirect calorimetry, and body temperature and total locomotor activity were measured by an implanted transponder. Leptin, etomoxir, or vehicle was administered intraperitoneally. Results : The temperature dependence of the metabolic rate of mature ob/ob and db/db mice were similar to that in wild‐type mice. In young 6‐week‐old ob/ob mice, the metabolic rate was almost doubled at 15 °C. Leptin (2 × 3 mg/kg) decreased the respiratory quotient (RQ) and carbon dioxide production but did not alter oxygen consumption, body temperature, or locomotor activity in ob/ob and C57BL/6J mice and had no effect in the db/db mice. Etomoxir (2 × 30 mg/kg) enhanced RQ and decreased oxygen consumption, carbon dioxide production, and body temperature in ob/ob, C57BL/6J, and db/db mice. Total locomotor activity was reduced in ob/ob and C57BL/6J mice. Discussion : In young ob/ob mice, the temperature sensitivity was enhanced compared with mature mice. Leptin and etomoxir had opposite effects on metabolic substrate preference. Leptin and lowered environmental temperature increased the relative fat oxidation as indicated by decreased RQ, possibly through activation of the sympathetic nervous system.     

Differences in demographic traits of four butterflyfish species between two reefs of the Great Barrier Reef separated by 1,200?km

Many species demonstrate variation in life history attributes in response to gradients in environmental conditions. For fishes, major drivers of life history variation are changes in temperature and food availability. This study examined large-scale variation in the demography of four species of butterflyfishes (Chaetodon citrinellus, Chaetodon lunulatus, Chaetodon melannotus, and Chaetodon trifascialis) between two locations on Australia’s Great Barrier Reef (Lizard Island and One Tree Island, separated by approximately 1,200 km). Variation in age-based demographic parameters was assessed using the re-parameterised von Bertalanffy growth function. All species displayed measurable differences in body size between locations, with individuals achieving a larger adult size at the higher latitude site (One Tree Island) for three of the four species examined. Resources and abundances of the study species were also measured, revealing some significant differences between locations. For example, for C. trifascialis, there was no difference in its preferred resource or in abundance between locations, yet it achieved a larger body size at the higher latitude location, suggesting a response to temperature. For some species, resources and abundances did vary between locations, limiting the ability to distinguish between a demographic response to temperature as opposed to a response to food or competition. Future studies of life histories and demographics at large spatial scales will need to consider the potentially confounding roles of temperature, resource usage and availability, and abundance/competition to disentangle the effects of these environmental variables.     

The energetics of the common mole rat Cryptomyś, a subterranean eusocial rodent from Zambia

Body temperature, oxygen consumption, respiratory and cardiac activity and body mass loss were measured in six females and four males of the subterranean Zambian mole rat Cryptomys sp. (karyotype 2 n=68), at ambient temperatures between 10 and 35°C. Mean body temperature ranged between 36.1 and 33.2°C at ambient temperatures of 32.5–10°C and was lower in females (32.7°C) than in males (33.9°C) at ambient temperatures of 10°C but dit not differ at thermoneutrality (32.5°C). Except for body temperature, mean values of all other parameters were lowest at thermoneutrality. Mean basal oxygen consumption of 0.76 ml O₂·g^-1· h^-1 was significantly lower than expected according to allometric equations and was different in the two sexes (females: 0.82 ml O₂·g^-1·h^-1, males: 0.68 ml O₂·g¹·h^-1) but was not correlated with body mass within the sexes. Basal respiratory rate of 74·min^-1 (females: 66·min¹, males: 87·min^-1) and basal heart rate of 200·min^-1 (females: 190·min^-1, males: 216·min^-1) were almost 30% lower than predicted, and the calculated thermal conductance of 0.144 ml O₂·g^-1·h¹·°C^-1 (females; 0.153 ml O₂·g^-1·h^-1·°C^-1, males: 0.131 ml O₂·g^-1·h^-1·°C^-1) was significantly higher than expected. The body mass loss in resting mole rats of 8.6–14.1%·day^-1 was high and in percentages higher in females than in males. Oxygen consumption and body mass loss as well as respiratory and cardiac activity increased at higher and lower than thermoneutral temperatures. The regulatory increase in O₂ demand below thermoneutrality was mainly saturated by increasing tidal volume but at ambient temperatures <15°C, the additional oxygen consumption was regulated by increasing frequency with slightly decreasing tidal volume. Likewise, the additional blood transport capacity was mainly effected by an increasing stroke volume while there was only a slight increase of heart frequency. In an additional field study, temperatures and humidity in different burrow systems have been determined and compared to environmental conditions above ground. Constant temperatures in the nest area 70 cm below ground between 26 and 28°C facilitate low resting metabolic rates, and high relative humidity minimizes evaporative water loss but both cause thermoregulatory problems such as overheating while digging. In 13–16 cm deep foraging tunnels, temperature fluctuations were higher following the above ground fluctuations with a time lag. Dominant breeding females had remarkably low body temperatures of 31.5–32.3°C at ambient temperatures of 20°C and appeared to be torpid. This reversible hypothermy and particular social structure involving division of labour are discussed as a strategy reducing energy expenditure in these eusocial subterranean animals with high foraging costs.Abbreviations BMR basal metabolic rate - br breath - C thermal conductance - HR neart rate - LD light/dark - M _b body mass - MR metabolic rate - OP oxygen pulse - PCO₂ partial pressure of carbon dioxide - PO₂ partial pressure of oxygen - RMR resting metabolic rate - RR respiratory rate - T _a ambient temperature - T _b body temperature - TNZ thermal neural zone - O₂ oxygen consumption     

Temperaturadaptation und Sauerstoffverbrauch bei Eidechsen

Zusammenfassung 1. Verschiedene Arten der GattungLacerta haben bei einer gleichbleibenden gemäßigten und hohen Temperatur eine verschiedene Stoffwechselintensität. Bei niedrigen Temperaturen verschwinden diese Unterschiede.2. Der Prozeß der thermischen Adaptation an die neue Temperatur geht auf zwei Weisen vor sich. Bei einzelnen Arten (Lacerta melisellensis undL. oxycephala) verläuft der Adaptationsprozeß von Anfang an ständig in der Richtung des Erreichens jener Werte des Stoffwechsels, welche das ruhende Tier bei der früheren Adaptationstemperatur hatte. BeiLacerta sicula dagegen fällt die Intensität des Stoffwechsels in den ersten Tagen des Aufenthaltes bei niederen Temperaturen, um später anzusteigen und sich jenem Wert zu nähern, den die Tiere bei ihren früheren Adaptationstemperaturen hatte.3. Die EidechsenLacerta melisellensis undL. oxycephala zeigen bei jeder Adaptationstemperatur nach Beendigung des Adaptationsprozesses die gleiche Intensität des Sauerstoffverbrauches. BeiLacerta muralis ist der Sauerstoffverbrauch bei einer höheren Adaptationstemperatur höher als bei einer niedrigeren.4. Bei Adaptation an eine neue, annähernd gleichbleibende Außentemperatur bleibt die Körpertemperatur praktisch unverändert. Auf diese Weise wird der Stoffwechsel des ruhenden Tieres in gewisser Hinsicht von der Höhe der Körpertemperatur während des Adaptationsprozesses unabhängig.

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Temperature adaptation and oxygen consumption in lizards

In some lizards the process of thermal adaptation and oxygen consumption at adaptation temperatures has been examined after completion of adaptation. A slow decrease of oxygen consumption was found for a certain period inLacerta sicula after transfer from a warm into a cold surrounding. The values of oxygen consumption increased from the ninth day and reached values corresponding to the new external temperature after about 3 weeks. InL. melisellensis andL. oxycephala adaptation to a new lower temperature occurs with the beginning of the increasing oxygen consumption, the adaptation lasting about 3 weeks. InL. muralis oxygen consumption at low adaptation temperature is lower after the process of adaptation than at higher adaptation temperature. In contrast, oxygen consumption ofL. melisellensis andL. oxycephala after adaptation to lower external temperatures is equal to the oxygen consumption at higher external temperatures, so that the animal shows the same intensity of oxygen consumption in spite of its different body temperature.

     

Oxygen consumption and flight muscle activity during heating in workers and drones of Apis mellifera

Summary Instantaneous oxygen consumption, muscle potential frequency, thoracic and ambient temperature were simultaneously measured during heating in individual workers and drones of honey bees. Relationships between these parameters and effects of thoracic temperature on power input and temperature elevation were studied. Oxygen consumption increased above basal levels only when flight muscles became active. Increasing muscle potential frequencies correlated with elevated oxygen consumption and raised thoracic temperature. The difference between thoracic and ambient temperature and oxygen consumption were linearly related. Oxygen consumption per muscle potential (l O₂ · g _–1 ^thorax · MP^–1) was two-fold higher in drones than in workers. However, oxygen consumption for heating the thorax (l O₂ · g _–1 ^thorax · (T_th-T_a) · °C^–1) was nearly the same in workers and drones. Thoracic temperature affected the amount of oxygen consumed per muscle potential (R₁₀=1.5). Achieved temperature elevation per 100 MP was more temperature sensitive in drones (R₁₀=6–10) than in workers (R₁₀=3.6). Q₁₀ values for oxygen consumption were 3 in workers and 4.5–6 in drones. Muscle potential frequency decreased with a Q₁₀=1.8 in workers and 2.7 in drones. Heating behaviour of workers and drones was different. Drones generated heat less continuously than workers, and showed greater interindividual variability in predilection to heat. However, the maximal difference between ambient and thoracic temperature observed was 22 °C in drones and 14 °C in workers, indicating greater potential for drones.Abbreviations DL dorsal-longitudinal muscle - DV dorsoventral muscle - MP muscle potential - T _a ambient temperature - T _th thoracic temperature