scholarly journals Telemetry Measured Body Temperature of Domestic Fowl at Various Ambient Temperatures

1978 ◽  
Vol 57 (4) ◽  
pp. 1075-1080 ◽  
Author(s):  
H. KADONO ◽  
E.L. BESCH
Keyword(s):  
Body Temperature ◽  
Domestic Fowl ◽  
Ambient Temperatures

scholarly journals Diurnal Body Temperature and Rate of Passage of Loggers in Lions

Animals ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 1388
Author(s):  
Ted Friend ◽  
Giulia Corsini ◽  
Vincent Manero ◽  
Raffaella Cocco
Keyword(s):  
Body Temperature ◽  
Time Frame ◽  
Heat Lamp ◽  
Future Studies ◽  
Ambient Temperatures ◽  
Diurnal Patterns ◽  
Data Loggers ◽  
The Mean ◽  
African Lions ◽  
Circadian Patterns

The documentation of diurnal patterns in body temperature in lions could be important because disruption of circadian patterns can be a useful measure of distress. This study quantified changes in body temperature of seven African lions (Panthera leo) at 5 min intervals during cold conditions from noon until the ingested body temperature loggers were expelled the next day. Thirteen loggers were fed to 11 lions during their daily noon feeding, while ambient temperatures were also recorded using six data loggers. The lions had continuous access to their dens and exercise pens during the day but were restricted to their heavily bedded dens that also contained a heat lamp from 23:00 until 08:00 the next day. Body temperatures averaged 37.95 ± 0.42 °C at 15:50, and 36.81 ± 0.17 °C at 06:50 the next day, 30 min before the first loggers passed from a lion, and were significantly different (t-test, t = 8.09, df = 6, p < 0.0003). The mean duration for the time of passage was 22 ± 2.69 (h ± SD), so future studies using the noninvasive feeding of temperature loggers need to consider that time frame.

Ambient temperature effects on physiological traits of white-tailed deer

1975 ◽  
Vol 53 (6) ◽  
pp. 679-685 ◽  
Author(s):  
J. B. Holter ◽  
W. E. Urban Jr. ◽  
H. H. Hayes ◽  
H. Silver ◽  
H. R. Skutt
Keyword(s):  
Heart Rate ◽  
Body Temperature ◽  
Energy Expenditure ◽  
Ambient Temperature ◽  
Temperature Effects ◽  
Temperature Changes ◽  
Wind Chill ◽  
Ambient Temperatures ◽  
Energy Equilibrium ◽  
Body Energy

Six adult white-tailed deer (Odocoileus virginianus borealis) were exposed to 165 periods of 12 consecutive hours of controlled constant ambient temperature in an indirect respiration calorimeter. Temperatures among periods varied from 38 to 0 (summer) or to −20C (fall, winter, spring). Traits measured were energy expenditure (metabolic rate), proportion of time spent standing, heart rate, and body temperature, the latter two using telemetry. The deer used body posture extensively as a means of maintaining body energy equilibrium. Energy expenditure was increased at low ambient temperature to combat cold and to maintain relatively constant body temperature. Changes in heart rate paralleled changes in energy expenditure. In a limited number of comparisons, slight wind chill was combatted through behavioral means with no effect on energy expenditure. The reaction of deer to varying ambient temperatures was not the same in all seasons of the year.

scholarly journals Body Temperatures in Some Australian Mammals II.Peramelidae

1962 ◽  
Vol 15 (2) ◽  
pp. 386 ◽  
Author(s):  
PR Morrison
Keyword(s):  
Body Temperature ◽  
Ambient Temperature ◽  
Active Phase ◽  
Temperature Measurements ◽  
Temperature Cycle ◽  
Body Temperatures ◽  
Ambient Temperatures ◽  
Diurnal Temperature

Body temperature measurements on the short-nosed bandicoot (Thylacis obeaulus) have shown a nocturnal cycle with a range of 1� 2�C and a short active phase at 2200-0400 hr. The bilby or rabbit bandicoot (Macrotis lagoti8) had a sharply defined temperature cycle, with a range of almost 3�C after several months of captivity, during which the day-time resting temperature was progressively lowered from 36� 4 to 34� 2�C. Forced activity raised the diurnal temperature substantially but not to the nocturnal level. Forced activity did not raise the nocturnal level which was similar in the two species (37' O�C). Both species could regulate effectively at an ambient temperature of 5�C, but only Thylaci8 showed regulation at ambient temperatures of between 30 and 40�C.

scholarly journals Nocturnal Hypothermia in Seasonally Acclimatized Mountain Chickadees and Juniper Titmice

The Condor ◽  
2005 ◽  
Vol 107 (1) ◽  
pp. 151-155 ◽  
Author(s):  
Sheldon J. Cooper ◽  
James A. Gessaman
Keyword(s):  
Body Temperature ◽  
Body Mass ◽  
Energy Savings ◽  
Ambient Temperatures ◽  
Energy Expenditures ◽  
Poecile Gambeli ◽  
Daily Energy ◽  
Para Determinar ◽  
Mountain Chickadees

AbstractWe measured body temperature of Mountain Chickadees (Poecile gambeli) and Juniper Titmice (Baeolophus ridgwayi) at different times of day and under a range of ambient temperatures in order to determine the use of nocturnal hypothermia in seasonally acclimatized small passerines. Our findings show both species used nocturnal hypothermia year-round. Depth of hypothermia was inversely correlated to body mass in Juniper Titmice but not in Mountain Chickadees. In both species, depth of hypothermia did not vary seasonally but nocturnal body temperature was regulated 3–11°C lower than daytime values. Nocturnal energy savings range from 7%–50% in chickadees and from 10%–28% in titmice. These nocturnal energy savings translate into ecologically important reductions in daily energy expenditures for these two species.Hipotermia Nocturna en Individuos de Poecile gambeli y Baeolophus ridgwayi Aclimatados EstacionalmenteResumen. Medimos la temperatura corporal de Poecile gambeli y Baeolophus ridgwayi a diferentes horas del día y en un rango de temperaturas ambientales para determinar el uso de hipotermia nocturna en pequeñas aves paserinas aclimatadas estacionalmente. Nuestros resultados muestran que ambas especies presentaron hipotermia nocturna durante todo el año. La profundidad de la hipotermia estuvo inversamente correlacionada con la masa corporal en B. ridgwayi, pero no en P. gambeli. En ambas especies, la profundidad de la hipotermia no varió estacionalmente, pero la temperatura corporal nocturna estuvo regulada 3–11°C por debajo de los valores diurnos. El ahorro nocturno de energía varió entre 7%–50% en P. gambeli y entre 10%–28% en B. ridgwayi. Estos ahorros nocturnos de energía se tradujeron en reducciones ecológicamente importantes en los gastos diarios de energía para ambas especies.

Dual core and shell temperature regulation during sea acclimatization in Gentoo penguins (Pygoscelis papua)

1994 ◽  
Vol 266 (4) ◽  
pp. R1319-R1326 ◽  
Author(s):  
E. Dumonteil ◽  
H. Barre ◽  
J. L. Rouanet ◽  
M. Diarra ◽  
J. Bouvier
Keyword(s):  
Body Temperature ◽  
Metabolic Rate ◽  
Thermal Insulation ◽  
Cold Water ◽  
Threshold Temperature ◽  
Ambient Temperatures ◽  
Adaptation To Cold ◽  
Marine Life ◽  
Shell Temperature ◽  
Skin Temperatures

Penguins are able to maintain a high and constant body temperature despite a thermally constraining environment. Evidence for progressive adaptation to cold and marine life was sought by comparing body and peripheral skin temperatures, metabolic rate, and thermal insulation in juvenile and adult Gentoo penguins exposed to various ambient temperatures in air (from -30 to +30 degrees C) and water (3-35 degrees C). Juvenile penguins in air showed metabolic and insulative capacities comparable with those displayed by adults. Both had a lower critical temperature (LCT) close to 0 degree C. In both adults and juveniles, the intercept of the metabolic curve with the abscissa at zero metabolic rate was far below body temperature. This was accompanied by a decrease in thermal insulation below LCT, allowing the preservation of a threshold temperature in the shell. However, this shell temperature maintenance was progressively abandoned in immersed penguins as adaptation to marine life developed, probably because of its prohibitive energy cost in water. Thus adaptation to cold air and to cold water does not rely on the same kind of reactions. Both of these strategies fail to follow the classical sequence linking metabolic and insulative reactions in the cold.

NPY Y1 receptor antagonist prevents NPY-induced torporlike hypothermia in cold-acclimated Siberian hamsters

2008 ◽  
Vol 294 (1) ◽  
pp. R236-R245 ◽  
Author(s):  
John Dark ◽  
Kimberly M. Pelz
Keyword(s):  
Body Temperature ◽  
Receptor Antagonist ◽  
Receptor Agonist ◽  
Phodopus Sungorus ◽  
Food Ingestion ◽  
Research Groups ◽  
Ambient Temperatures ◽  
Y1 Receptor ◽  
Siberian Hamsters ◽  
Intracerebroventricular Injections

Siberian hamsters ( Phodopus sungorus) undergo bouts of daily torpor during which body temperature decreases by as much as 20°C and provides a significant savings in energy expenditure. Natural torpor in this species is normally triggered by winterlike photoperiods and low ambient temperatures. Intracerebroventricular injection of neuropeptide Y (NPY) reliably induces torporlike hypothermia that resembles natural torpor. NPY-induced torporlike hypothermia is also produced by intracerebroventricular injections of an NPY Y1 receptor agonist but not by injections of an NPY Y5 receptor agonist. In this research, groups of cold-acclimated Siberian hamsters were either coinjected with a Y1 receptor antagonist (1229U91) and NPY or were coinjected with a Y5 receptor antagonist ( CGP71683 ) and NPY in counterbalanced designs. Paired vehicle + NPY induced torporlike hypothermia in 92% of the hamsters, whereas coinjection of Y1 antagonist + NPY induced torporlike hypothermia in 4% of the hamsters. In contrast, paired injections of vehicle + NPY and Y5 antagonist + NPY induced torporlike hypothermia in 100% and 91% of the hamsters, respectively. Although Y5 antagonist treatment alone had no effect on body temperature, Y1 antagonist injections produced hyperthermia compared with controls. Both Y1 antagonist and Y5 antagonist injections significantly reduced food ingestion 24 h after treatment. We conclude that activation of NPY 1 receptors is both sufficient and necessary for NPY-induced torporlike hypothermia.

The metabolic rate and thermal conductance of the eastern barred bandicoot (Perameles gunnii) at different ambient temperatures

2003 ◽  
Vol 51 (6) ◽  
pp. 603 ◽  
Author(s):  
M. P. Ikonomopoulou ◽  
R. W. Rose
Keyword(s):  
Oxygen Consumption ◽  
Body Temperature ◽  
Metabolic Rate ◽  
Thermal Conductance ◽  
The Body ◽  
High Metabolic Rate ◽  
Ambient Temperatures ◽  
Reduced Body ◽  
Thermoneutral Zone ◽  
Reproductive Females

We investigated the metabolic rate, thermoneutral zone and thermal conductance of the eastern barred bandicoot in Tasmania. Five adult eastern barred bandicoots (two males, three non-reproductive females) were tested at temperatures of 3, 10, 15, 20, 25, 30, 35 and 40°C. The thermoneutral zone was calculated from oxygen consumption and body temperature, measured during the daytime: their normal resting phase. It was found that the thermoneutral zone lies between 25°C and 30°C, with a minimum metabolic rate of 0.51 mL g–1 h–1 and body temperature of 35.8°C. At cooler ambient temperatures (3–20°C) the body temperature decreased to approximately 34.0°C while the metabolic rate increased from 0.7 to 1.3 mL g–1�h–1. At high temperatures (35°C and 40°C) both body temperature (36.9–38.7°C) and metabolic rate (1.0–1.5 mL g–1 h–1) rose. Thermal conductance was low below an ambient temperature of 30°C but increased significantly at higher temperatures. The low thermal conductance (due, in part, to good insulation, a reduced body temperature at lower ambient temperatures, combined with a relatively high metabolic rate) suggests that this species is well adapted to cooler environments but it could not thermoregulate easily at temperatures above 30°C.

Temperature regulation

2017 ◽  
Author(s):  
Bareket Falk ◽  
Raffy Dotan
Keyword(s):  
Body Temperature ◽  
Children And Adolescents ◽  
Temperature Regulation ◽  
Heat Dissipation ◽  
Epidemiological Data ◽  
Skin Surface ◽  
Neutral Zone ◽  
Sweat Loss ◽  
Ambient Temperatures ◽  
Dry Heat

Under all but the most extreme environmental heat conditions, children control their body temperature (at rest and during exercise) as well as adults. Children, however, use a different thermoregulatory strategy. Compared with adults, children rely more on dry heat dissipation and less on evaporative cooling (sweating). Their larger skin surface-area relative to mass does put children at increasing disadvantage, relative to adults, as ambient temperatures rise above skin temperature. Similarly, they become increasingly disadvantaged upon exposure to decreasing temperatures below the thermo-neutral zone. Like adults, children inadvertently dehydrate while exercising in hot conditions and are often hypohydrated, even before exercise, and their core temperature rises considerably more than adults in response to a given fluid (sweat) loss, which may put them at higher risk for heat-related injury. However, epidemiological data show rates of both heat- and cold-related injuries among children and adolescents as similar or lower than at any other age.

Responses of conscious rabbits to CO2 at ambient temperatures of 5, 20, and 35 degrees C

1979 ◽  
Vol 47 (3) ◽  
pp. 522-526 ◽  
Author(s):  
M. Maskrey ◽  
S. C. Nicol
Keyword(s):  
Body Temperature ◽  
Brain Stem ◽  
Minute Volume ◽  
Atmospheric Air ◽  
Co2 Partial Pressure ◽  
Ambient Temperatures ◽  
Stretch Receptors ◽  
Pulmonary Stretch Receptors ◽  
Conscious Rabbits ◽  
The Brain

Conscious rabbits were exposed to atmospheric air or to 6% CO2 in air at ambient temperatures (Ta) of 5, 20 and 35 degrees C. Measurements were made of rectal temperature (Tre), metabolic rate (MR), respiratory frequency (f), tidal volume (VT), and minute volume (VE). CO2 exposure did not affect Tre at any Ta and only affected MR at 35 degrees C when it caused an increase. At each Ta hypercapnia caused an increase in VT and a decrease in f. At 5 degrees C VE was increased by CO2, at 35 degrees C VE decreased, and at 20 degrees C the results were variable. The data were examined in the light of theories relating to the relative contributions of inputs from brain stem and from pulmonary stretch receptors, in response to body temperature and CO2 partial pressure. It was concluded that hypercapnia stimulates an increase in VT via the brain stem, whereas at the same time removing a hypocapnic drive which, along with central thermal inputs, stimulates f.

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