Air flow and convective heat loss from small mammals in laboratory metabolism chambers

1. 1.Thermal conductance was determined from cooling curves of Mus domesticus carcasses at air flow rates ranging from still air to 0.91·min⁻¹ STP. Thermal conductance was constant over this range of air flows. This indicates that free convection predominates over forced convection at these air flow rates.

2. 2.While non single set of conditions will be appropriate for all experiments, free convection conditions are appropriate for determination of minimal thermal conductance.

Energy budget of the chicken foot

1. 1.|A mathematical model predicts the energy loss from a chicken foot provided the following variables are known: body temperature, air temperature, wind velocity, blood flow to the foot, and the relative partitioning of blood flow via two distinct venous returns.

2. 2.|Chickens are capable of keeping their feet from freezing at temperatures as low as −30°C ambient, but at a high energy cost.

3. 3.|Chickens can modulate blood flow to their feet at thermoneutral temperatures enough to vary heat loss to environment by about one-fourth metabolic heat production.

Heat-transfer relations of avian nestlings

1. 1.|To determine the thermoregulatory prowess of altricial nestlings, we conducted both equilibrium and transient analyses of white-crowned sparrow nestings, a representative fringillid.

2. 2.|For an individual nestling at thermal equilibrium, feather development is the major factor reducing heat loss after 2 days of age; tissue- and boundary-layer resistances are of minor importance.

3. 3.|The nest substantially reduces wind speeds near the nestlings. Heat transfer through the nest material is of only moderate importance. Evaporation also appears to be a small proportion of total heat loss during hypothermia in natural environments.

4. 4.|Net long-wave radiant exchange is also minor, but short-wave radiation is potentially a major component of the nestling's energy budget, approaching the magnitude of maximal metabolic heat production.

5. 5.|When nestlings cool, their body mass and metabolic rate are also major importance in determining the rate of cooling, and (for metabolism) the equilibrium temperature as well.

6. 6.|The huddling together of nestlings is perhaps the single most important factor affecting heat transfer.

7. 7.|An older brood actually has more insulation than does an adult in the same microclimate.

Blockage errors in studies of the effect of wind on thermoregulatory responses

1. 1.The presence of an animal in a wind tunnel increases the effective wind velocity, and so increases heat transfer rates.

2. 2.Potentially significant errors in thermal conductance and thermoregulatory metabolism measurements may result.

3. 3.In a given wind tunnel metabolism chamber, these errors are size dependent and thus may lead to invalid allometric or adaptive interpretations of data.

4. 4.The errors are also sensitive to the shape, orientation, and characteristics of the fur or feather insulation of the animal. Thus, only approximate guidelines can be given for choosing correction factors.

Heat stress and age: Skin blood flow and body temperature

1. 1. The ability to increase skin blood flow is an important mechanism for transferring heat from the body core to the skin for dissipation.

2. 2. During exercise, skin blood flow is typically 20–40% lower in men and women aged 55 and over (compared with 20–30 years old) at a given body core temperature. Yet criterion measures of heat tolerance (changes in core temperature, heat storage) often show minimal or no age-related alterations. From a series of studies conducted in our laboratory over the past 5 years, the following conclusions can be drawn.

3. 3. When fit healthy older subjects are matched with younger subjects of the same gender, size and body composition, V_O2max, acclimation state, and hydration level, age-related differences in skin blood flow are evident. However, these differences often do not translate into “poorer” heat tolerance or higher core temperatures.

4. 4. The larger core-to-skin thermal gradient maintained by the older individuals allows for effective heat transfer at lower skin blood flows.

5. 5. Furthermore, there is an increased coefficient of variation for thermoregulatory response variables with increasing age.

6. 6. Despite differences in the mechanisms underlying thermoregulation, true thermal tolerance is less a function of chronological age than of functional capacity and physiological health status.

7. 7. While this conclusion is based primarily on cross-sectional studies, it is supported by the results of more recent studies using multiple regression analyses.

8. 8. Implicit in this conclusion is the notion that thermal tolerance, at any age, is a modifiable individual characteristic.

Heat flow of the paraplegic and able-bodied lower limb during resting heat exposure

1. The heat flow of paraplegic (PA) and able-bodied (AB) subjects were determined at rest in cool and warm conditions.

2. During heat exposure upper body sites for both groups showed heat loss, whereas the lower body sites of the PA groups showed heat gain.

3. During heat exposure, a systematic difference between groups in the relationship between heat flow and calf-skin temperature existed.

4. In conclusion, heat storage appears to be localised in PA subjects at rest and centralised for AB subjects.

Transient response of the human-clothing system

1. 1. A transient clothing model which considers the effects of adsorption and thermal capacitance on the dynamic thermal response of clothing was developed.

2. 2. Moisture adsorption and desorption by the fabric are the major factors that affect the transient response of clothing.

3. 3. This moisture can come from evaporated sweat or from the environment.

4. 4. The clothing model was combined with a modified version of the two-node thermal model of the human body.

5. 5. The combined model shows that, during transients, the mix of latent and sensible heat flow from the skin may differ considerably from the corresponding heat flows from the clothing surface to the environment.

6. 6. The alteration of the heat flows can have a significant impact on the thermal response of the body by changing the sweat rate required to achieve the heat loss necessary to maintain thermal balance.

Factors affecting the resistance to heat transfer provided by clothing

1. 1. This paper discusses the factors that affect the insulation and evaporative resistance provided by clothing.

2. 2. These include: fabric thickness and density, the amount of body surface area covered by garments, the evenness of the distribution of fabrics over the body surface, the increase in surface area for heat loss due to clothing, the looseness or tightness of fit, a person's body position (seated vs standing), body motion and wind.

Why are small homeotherms born naked? Insulation and the critical radius concept

1. 1. For cylinders or spheres smaller than a critical size, a layer of insulation may increase, rather than decrease, the rate of heat exchange.

2. 2. It has been suggested that the critical size for animals insulated with fur or feathers is about 4–7 g body mass, and therefore may explain why many small mammals and birds are born naked. We suggest that this is unlikely.

3. 3. We found that downy feathers on hatchlings as small as 1.6 g body mass retard rates of heat loss. Also, hatchling birds smaller than 4–7 g are not always, or even often, born naked.

4. 4. If a critical size exists at all, it is likely to occur at body masses of 0.6 g or smaller.

Some effects of thyroidectomy on growth, heat production and the thermoregulatory ability of the immature fowl (Gallus domesticus)

1. 1.|The effect of thyroidectomy at 12 days of age on weight gain, and on heat production and thermoregulatory ability of 4- to 5-week-old chickens at temperatures within and below the thermo-neutral zone was investigated.

2. 2.|Despit the absence of thyroid tissue, as demonstrated with radioiodine, a small amount of thyroxine was found in the plasma of some thyroidectomized (TX) birds.

3. 3.|Thyroidectomy depressed weight gain; pair-fed controls grew significantly faster than TX birds.

4. 4.|Resting heat production of TX birds at thermoneutrality (30°C) was depressed by 18% (P < 0.001) and body temperature by 0.4°C (P < 0.001).

5. 5.|At 12°C heat production of TX birds was similar to that of controls but the body temperature of TX birds was 0.7°C lower (P < 0.001).

6. 6.|Thyroidectomized birds were unable to regulate body temperature at 5°C even if thyroxine was provided on the day before and at the time of cold-exposure. This inability to thermoregulate was probably due to inadequate insulation and poor nutritional status.

Direct heat injury of roots of woody swamp species

1. 1.Three month-old seedlings of Taxodium distichum, Nyssa aquatica, Cephalanthus occidentalis and cuttings of Salix nigra were acclimated to simulated natural swamp conditions (ambient temperature, saturated soil) and then used to assess direct high temperature injury of root tissue.

2. 2.Electrolyte leakage from excised root tissue exposed for 30 min to temperatures ranging from 30 to 66°C was used to assess cellular injury.

3. 3.The relationship between leakage and temperature was sigmoidal for each species.

4. 4.Inflection point temperatures on the response curves, ranged from 45.4 to 51.0°C, were species-specific, and indicated differences in thermal tolerance of root membranes.

5. 5.Root of C. occidentalis and N. aquatica were more heat tolerant than roots of T. distichum and S. nigra.

Effect of warm rearing on temperature regulation in resting and exercising rats

1. 1.|Hypothalamic and rectal temperatures were recorded in 8 warm-reared (wr) and in 12 warm-acclimated control rats during resting in the heat and during 30 min running under thermoneutral conditions.

2. 2.|Brain and body temperatures of wr rats were significantly higher (P < 0.001) than control rats, both in normothermia as well as in hyperthermia; at rest, and also during exercise.

3. 3.|Warm-reared rats were more tolerant to heat.

4. 4.|During normothermia a weak selective brain cooling was present in control but absent in wr rats. During hyperthermia, however, the cooling intensified in control and occurred in wr rats.

5. 5.|The main strategy of adaptation to heat in wr rats is an upward resetting of the temperature set-point and increased passivity.

Two types of heat tolerance in FHM-cells. Induction by heat-shock versus elevated culturing temperature

1. 1.Increased heat tolerance in FHM-cells from Pimephales promelas (Pisces) can be induced by culturing the cells at elevated temperatures (heat resistant acclimation) as well as by heat shock (heat hardening).

2. 2.After shift of culturing temperature (CT) from 16 to 32°C both effects are detectable with different temporal patterns.

3. 3.Cellular concentrations of heat-shock proteins correlate with the hardening effect but not with heat resistance acclimation.

4. 4.Several culturing temperature specific proteins were detected. The patterns of some enzymes are also altered by culturing temperature.

5. 5.Heat resistance acclimation is not caused by selection of a thermoresistant subpopulation of cells.

6. 6.Heat hardening and heat resistance acclimation must be distinguished as different phenomena in FHM-cells.

Adaptation of industrial/commercial air conditioners for use in a thermally stressful environment

1. 1. The concept of intermittent, microclimate cooling during rest periods has been investigated due to the logistical and ergonomic problems associated with backpack cooling systems

2. 2. In an attempt to improve intermittent cooling applications, the use of industrial/commercial air conditioners (ICAC) as a source of cool air was conceived

3. 3. In the current study, a prototype of a pressurized air distribution unit (PADU) which can be incorporated into existing ICAC was designed and fabricated

4. 4. In a successful test, an ICAC circulated air and cooled it down to the set temperature, while the PADU pumped 5101/min (the specified air volume for one person) of 15°C into each air cooling vest, 4601/min to the body and 501/min to the face, through filters and 10 ft/1 in. diameter supply line

5. 5. The PADU is necessary to increase the air pressure in the system, creating the required air volume

6. 6. This promising concept adapts existing ICAC to provide adequate amounts of clean, cool air to individuals working in thermally stressful environments

7. 7. This development effectively increases the conditioned air sources available for use in decreasing heat storage and increasing personal comfort in military or civilian scenarios where work is conducted in protective garments.

Functions of fat in hibernators: Thermal aspects

1. 1.|A numerical, distributed parameter model of heat exchange is used to evaluate the thermal significance of the presence and placement of subcutaneous fat in hibernating marmots. The model is most sensitive to changes in conductivity and metabolic rate of muscle tissue, parameters which are known to greater precision than are others in the model.

2. 2.|Alternative models are developed for animals with fat located dorsally and with no fat at all.

3. 3.|A comparison of these three models shown that there is no difference in the metabolic output required to maintain body temperature among the three alternatives. Therefore, neither the presence nor the location of fat serves an insulative role in hibernators.

Effect of hyperthermia on blood constituents in the domestic rabbit (Lepus cuniculus)

1. 1. Effects of exposing rabbits to temperatures 37–50°C on body-core temperature and some blood constituents were investigated.

2. 2. Heat stroke death occurred at or above a critical core-temperature of 43.0°C.

3. 3. Plasma osmolality and levels of glucose, urea and lactate were significantly elevated in hyperthermia.

4. 4. Widespread tissue damage was indicated by increases in plasma activities of glutamate oxaloacetate transaminase (GOT), glutamate pyruvate transaminase (GPT) and creatinine phosphokinase (CPK).

5. 5. The most sensitive indicators of impending heat stroke in heat stressed rabbits were plasma levels or urea, lactate and CPK.

Thermosensitivity during embryonic development of Lymnaea stagnalis (Mollusca)

1. 1.|The percentage of survival after 1 hr at 40.0°C is lowest at the larval trochophore stage and at hatching of the young snail.

2. 2.|Heat resistance depends on the stage of development.

3. 3.|From the early cleavage stage onwards a higher percentage of embryos can withstand high temperature after a previous heat treatment than without it.

4. 4.|The pattern of thermosensitivity is discussed in relation to the organizational level of the stage of development.

5. 5.|It is concluded that the developing Lymnaea is a suitable system to study heat resistance and thermotolerance at the level of cells, organs and organism.

Cardiovascular and thermoregulatory responses to repeated anticholinesterase administration

1. 1.|Pyridostigmine administration decreased resting heart rate by 11 ± 7 beats/min and resting oesophageal temperature by 0.23 ± 12°C after 50 h (P < 0.05). In addition, red blood cell cholinesterase activity was decreased an average of 43 ± 7% after 50 h of pyridostigmine treatment.

2. 2.|The lower heart rates and core temperatures at rest were continued during high intensity exercise in a 35°C environment. Whole body sweating was 12 ± 18% higher (P = 0.20) during exercise in the heat after 50 h of pyridostigmine treatment.

3. 3.|Repeated anticholinesterase administration had little effect on cardiovascular and thermoregulatory responses during high intensity exercise.

Temperature gradients in the nasal cavity of the rabbit

1. 1.|Temperatures at four sites along the ventral nasal concha were recorded in four unrestrained rabbits exposed to ambient temperatures from 0 to 35°C.

2. 2.|The nasal temperatures decreased and temperature gradients from proximal to distal parts of the concha increased in cold-exposed rabbits.

3. 3.|The temperature gradients increased also during panting in heat-stressed rabbits.

4. 4.|The ventral nasal concha is suggested to be an efficacious heat exchanger both in cold and hot ambient, due to its geometry and vascularization.

Characteristics of wettedness under constant average skin temperature

1. 1. Experiments were carried out concerning the characteristics of wettedness revealed under constant average skin temperature using sitting-resting nude subjects. From the basic measurements of both environmental parameters and human physiological responses, the conclusions detailed below were proposed regarding the changes of wettedness under constant average skin temperature.

2. 2. There is positive correlation between the wettedness and environmental humidity, and negative correlation between the wettedness and air temperature.

3. 3. There is positive correlation between the evaporative heat loss from the skin surface and air temperature, and negative correlation between the evaporative heat loss and environmental humidity.

4. 4. There is negative correlation between the wettedness and evaporative heat loss.

5. 5. Wettedness is not constant but takes varying values, that is, corresponding to each average skin temperature both the maximum and the minimum wettedness values occur.

6. 6. Deriving from the items mentioned above, the theoretical locus of equal average skin temperature is not a straight line, but is a curved line plotted on the psychrometric chart.