Do birds possess brown adipose tissue?

• 1.1. Fluorescence and electron microscopy were used to visualize differences between avian adipose tissue (AAT) collected from clavicular and abdominal regions of the great tit, the willow tit, the house sparrow and the Japanese quail, and interscapular brown adipose tissue (BAT) obtained from the Djungarian dwarf hamster.
• 2.2. Multilocular fat cells were found in AAT. The prerequisite for multilocularity, however, was not simply winter acclimatization [short photophase 4L:20D and low ambient temperature (< −20°C in January in Oulu)] or cold-acclimation (−25°C). Multilocular adipocytes were found during autumn and in unacclimated control birds as well. Mitochondria in the AAT were fewer and about one-sixth the length of those in BAT. This finding was associated with low cytochrome oxidase (COX) activity in the tissue homogenate and isolated mitochondrial fraction of the AAT (< 5.2% of that in BAT).
• 3.3. Catecholamine fluorescence was seen only around arteries in the AAT. Signs of sympathetic parenchymal innervation were found neither in winter- nor in cold-acclimated birds, but typically, sympathetic nerve fibers forming a basket-like network around every cell were seen in the brown fat of the hamster.
• 4.4. Our results show that AAT in the adult birds resembles white adipose tissue more than brown. Multilocularity of adipocytes may improve lipolysis to deliver fatty acids for muscle fuel of shivering or NST.

     

Sea-water tolerance in freshwater-resident arctic charr (Salvelinus alpinus)

• 1.1. Freshwater-resident Arctic charr acclimated for 2 months at 8°C, 15% were divided into four experimental groups in July and exposed to 1 and 8°C in 15 and 34% salinity.
• 2.2. Only slight changes in gill Na-K-ATPase activity, blood plasma osmolality and blood plasma concentrations of Cl⁻ and Mg²⁺ were found for the fish exposed to 1 or 8°C in brackish water.
• 3.3. When exposed to sea-water at 8°C, an increase in osmolality and in concentrations of Cl⁻ and Mg²⁺ took place during the first 2–3 days, after which it levelled off.
• 4.4. If exposed to sea-water at 1°C, however, marked increases were found for all parameters measured and all the fish were dead within 5 days of exposure.
• 5.5. These results show that freshwater-resident Arctic charr—if acclimated to brackish water—can survive in sea-water during summer if the environmental temperature is not too low.

     

Oxygen consumption in the tortoise,Testudo hermanni G., subjected to sudden temperature changes in summer and autumn

• 1.1. A respirometer for long-term measurements of oxygen consumption in terrestrial vertebrates is described.
• 2.2. The tortoise, Testudo hermanni Gmelin, investigated in summer and autumn, presents a day-night rhythm of oxygen consumption at 28 and 18°C but not at 8°C.
• 3.3. The standard metabolic rate presents an important and constant thermal dependence in the range 8-18-28°C.

     

The effect of temperature on the acid-base status of the blood of the hatching quail (Coturnix c. japonica)

• 1.1. The ambient temperature of embryos of pipped eggs was reduced from 38 to 28°C for a period of 45 min.
• 2.2. The blood P_CO2 was lower and the blood more alkaline at 28°C than at 38°C.
• 3.3. At 28°C plasma [HCO₃⁻] ] was lower than predicted from the blood buffer line determined in vitro.
• 4.4. The plasma concentrations of strong ions and lactate were the same at both temperatures.
• 5.5. After the ambient temperature had been returned to 38°C for a period of 45 min, blood pH was more acidic than before cooling, but there was no difference in blood P_CO2.
• 6.6. The plasma [HCO₃⁻] was the same as that at 28°C and plasma [K⁺] was higher than before cooling.
• 7.7. The results arc discussed in relation to the factors affecting blood pH in embryos at this stage of development.

     

The response of brown adipose tissue mitochondrial glycerolphosphate acyltransferase to cold-exposure in hypothyroidism,after adrenalectomy and after treatment with cycloheximide

• 1.1. Exposure to cold has previously been shown to considerably increase the activity of the mitochondrial form of glycerolphosphate acyltransferase (GPAT) in brown adipose tissue (A.C. Darnley C.A. Carpenter and E. D Saggerson, Biochem.J.253, 351–355, 1988; J.R.D. Mitchell and E.D. Saggerson. PBiochem.J.277, 665–669, 1991).
• 2.2. Both adrenalectomy and chemically-induced hypothyroidism increased mitochondrial GPAT activity in rats maintained at 21°C. This increase was similar to that caused by exposing rats to the cold (4°C) for three days. Whereas exposure of hypothyroid rats to cold (4°C) resulted in a further increase in GPAT activity, no further increase in activity was observed after exposure of adrenalectomized rats to the cold.
• 3.3. Administration of triiodothyronine (T₃) to rats maintained at 21°C had no effect on mitochondrial GPAT activity.
• 4.4. Prior treatment with cycloheximide abolished 60–70% of the increase in GPAT activity caused by cold-exposure.

     

The effects of temperature and moisture on survival capacity,cuticular permeability,hemolymph osmoregulation and metabolism in the scorpion,Centruroides hentzi (banks) (scorpiones,buthidae)

• 1.1. The temperature and water relations of Centruroides hentzi females were investigated. At 12 and 72% relative humidity (RH), the lower and upper Lt₅₀ were -4.5 and 43.7°C, and -4.7 and 45.1°C, respectively. When exposed to high temperature stress, survivorship was significantly greater under mesic conditions.
• 2.2. Cuticular water loss was higher under xeric conditions (12% RH), ranging from 0.061 mg/cm²/hr at 30°C to 0.211 at 41°C.
• 3.3. Exposure to dry air (0–5% RH) resulted in a significant increase in hemolymph osmolality: from 441 to 688 mOsm over a 5 day period.
• 4.4. Mean oxygen consumption rates increased from 161.7 mm³/g/hr at 34°C to 541.6 at 44°C. ATPase activity was significantly higher in animals acclimated and tested at 35°C.

     

Temperature acclimation in respiratory and cytochrome c oxidase activity in common carp (Cyprinus carpio)

• 1.1. Common carp (Cyprinus carpio) exposed to experimental temperatures of 12, 18, 24, 30 or 36°C for a 4-week period were used to investigate the effect of temperature acclimation on the frequency of opercular movement (FOM), growth and cytochrome c oxidase (CCO) activity in heart, liver and muscle.
• 2.2. An exponential relationship between FOM and temperature after the first week (10₁₀ =1.76) disappeared after the second week.
• 3.3. The initially high FOM at temperatures of 30 or 36°C and the low FOM at 18 or 12°C changed over 4 weeks to approach the FOM of fish at 24°C.
• 4.4. This change in the relationship of FOM to temperature from highly dependent to independent appeared to be thermal compensation.
• 5.5. Heart and liver CCO activities were significantly affected by temperature, with the lowest activity at the approximate optimum temperature for growth, 24°C.
• 6.6. Highest CCO activities for heart and liver occurred at both the highest and lowest temperatures.
• 7.7. Among the three tissues, heart CCO activity was generally the highest and most affected by acclimation temperature.
• 8.8. Muscle tissue had the lowest CCO activity and was unaffected by temperature.
• 9.9. The high CCO activity at a cold acclimation of temperature 12°C was probably due to thermal compensation and the high activity at 36°C may have been a result of thermal stress.

     

Effects of low temperatures on NAD-sorbitol dehydrogenase activity and morphogenesis in non-diapause eggs of the silkworm,Bombyx mori

• 1.1. The activity of NAD-sorbitol dehydrogenase (NAD-SDH; EC 1.1.1.14) and levels of sorbitol were examined in non-diapause eggs of the silkworm, Bombyx mori, exposed to temperatures of 20-0.5°C from 1 day after oviposition. The morphology of embryos in the cold-acclimated eggs and the hatching of eggs after transfer to 25°C were monitored.
• 2.2. Temperatures between 15 and 0.5°C retarded the development of NAD-SDH activity at a specific embryonic stage that was comparable to diapause, and sorbitol accumulated in the eggs.
• 3.3. With the appearance of NAD-SDH activity, sorbitol was converted into glycogen, just as it is in diapause eggs. The results indicate that NAD-SDH participates in the utilization of sorbitol rather than in its formation in non-diapause eggs.
• 4.4. Distinct effects of low temperatures on the morphological development of the embryos are also discussed.

     

Metabolic rate and body temperature of adult and juvenile hyrax (Procavia capensis)

• 1.1. Resting metabolic rates (RMR) below thermoneutrality in adult hyrax acclimated to 26, 15 and 10°C remained unchanged, i.e. thermal conductance (K) remained constant.
• 2.2. Conductance in juveniles decreased with acclimation to lower ambient temperatures (T_a).
• 3.3. Body temperature (T_b) dropped by 3.8°C in adults exposed to T_a of 30 – 5°C. The decrease was constant.
• 4.4. Body temperature fell by 1.5°C in juveniles exposed to T_a of 30 – 20°C but stabilized between 20 and 5°C.
• 5.5. The labile T_b, associated with behavioural strategies and lower than predicted RMR, can be seen as an energy-conserving mechanism of particular importance during winter conditions.

     

Heart rates of adult red-spotted newts,Notophthalmus viridescens in air and submerged in normoxic and hypoxic water at different temperatures

• 1.1. Heart rates of adult aquatic red-spotted newts can be conveniently recorded using an impedance pneumograph.
• 2.2. Heart rates decrease linearly with decreasing temperature.
• 3.3. Submergence in normoxic and hypoxic water at 10°, 15°, and 20°C results in bradycardia which is more pronounced in hypoxic water.
• 4.4. At 5°C one newt exhibited the above pattern, but bradycardia was not exhibited by the other newt during normoxic submergence.
• 5.5. Diminishing heart rates are probably due to oxygen deficiency, not immersion alone.
• 6.6. Recovery from bradycardia in air is rapid and not linked with resumption of aerial breathing.

     

Lactate dehydrogenase of goldfish red and white muscle in relation to thermal accumulation

• 1.1. Activities of the red and white muscle LDH from 8°C-acclimated goldfish were about three times higher than those acclimated to 28°C.
• 2.2. Isozyme composition and some kinetic properties of the red muscle LDH differed from those of the white muscle enzyme.
• 3.3. The amount of red muscle as well as LDH activity tended to increase during cold acclimation.

     

Influence of environmental factors on the deep and skin temperature in the European bison,Bison bonasus (L.)

• 1.1. In 43 European bison divided into three groups (Group A, 3–8-month-old calves; Group B, 18-month-7-year-old young bison; Group C, 12–24-year-old bison) the rectal, humerus region and abdomen region temperatures were measured.
• 2.2. The experiments were carried out in winter months, from mid-December to mid-March.
• 3.3. The mean rectal temperatures changed from 38.55°C in calves to 38.15°C in the oldest bison.
• 4.4. The mean temperatures of the humerus region changed from 20.69°C in calves to 21.49°C in older bison.
• 5.5. The mean temperatures of the abdomen region changed from 20.79°C in calves to 22.17°C in older bison (Gr. B).
• 6.6. The cluster analysis divided the bison into four groups named hot, warm, cool and cold bison.
• 7.7. Only air temperature measured 2 m above the ground and snow cover influenced the integrated bison temperature. Age, sex and mass as well as some environmental factors had no influence.
• 8.8. Measurements made 1 to nearly 4hr after a bison's death showed a drop in rectal temperature and mostly increases in temperatures of the humerus and abdomen regions.

     

Behavioural thermoregulation and critical thermal limits of Macrobrachium acanthurus (Wiegman)

• (1)The preferred temperatures of Macrobrachium acanthurus were determined for prawns acclimated to 20°C, 23°C, 26°C, 29°C and 32°C, and the final preferendum estimate was (29.5°C).
• (2)The critical thermal minima (CTMin) and maxima (CTMax) were 11.0°C, 12.1°C, 13.0°C and 14.8°C, and 34.2°C, 35.0°C, 36.1°C and 39.8°C, respectively.
• (3)The zone of thermal tolerance assessed using the CTMin and CTMax boundaries was 644°C².
• (4)The acclimation response ratio was between 0.33 and 0.62.
• (5)To cultivate this species in the southeastern region of México it should be done in not <15°C (CTMin) during the winter and below 38°C in summer (CTMax).

     

Bacterial endotoxin and infection cause behavioural hypothermia in infant mice

• 1.1. When placed in a temperature gradient, 3–10 day old mice injected with living Escherichia coli or with E. coli endotoxin, select 2–3°C lower temperatures than their litter-mate controls injected with saline.
• 2.2. At the lower selected temperature (32°C) young mouse pups resist bacterial infection for longer and tolerate higher doses of endotoxin than at the temperature selected by the controls (35°C).
• 3.3. It is possible that a controlled hypothermic state, here called cryexia, is in small mammals an alternative strategy to fever for coping with infections.

     

Plasma metabolites of lake trout (Salvelinus namaycush) in relation to diet and storage conditions

• 1.1. The effects of storage temperature (2, −20 and −80°C) and duration (3, 9 and 27 days) on plasma metabolites concentrations of lake trout fed three dietary protein levels (20, 40 and 60%) and a single lipid level (20%) for 28 days were investigated.
• 2.2. Significantly high plasma urea and glucose concentrations were associated with low (20%) and high (60%) dietary protein intake in fish; while, high plasma creatinine concentration seems to characterize insufficient dietary protein and energy consumption.
• 3.3. Deproteinization of plasma with 5.0% sulfosalicylic acid did not confer better storage stability for any of the plasma metabolites except ammonia which was significantly high in non-deproteinized samples when stored at 2°C over 3, 9 and 27 day periods.
• 4.4. These studies suggest that non-deproteinized fish plasma can be stored at − 20°C without affecting the baseline concentrations of ammonia, creatinine and glucose for up to 9 days and, urea and total protein for up to 27 days.

     

Analysis of clotting defects in diseased lobsters—I. Alterations in blood parameters

• 1.1. In gaffkemic lobsters kept at 15°C. drastic declines in the hemocyte number and clotting ability occur.
• 2.2. In animals kept at 10°C, although some clotting defects rapidly occur, a high number of amoebocytes is found. Clotting ability reappears after 5 days.
• 3.3. The proportion of each type of hemocyte changes. Numerous hemocytes show morphologic altered features.
• 4.4. Dorsal hematopoietic tissue is as in control lobsters.
• 5.5. Total protein contents are similar in bacteremic or control lobster hemolymphs.

     

Effects of low environmental pH and temperature on hatching and metabolic rates in embryos of Anax junius drury (Odonata: Aeshnidae) and the role of hypoxia in the hatching process

• 1.1. Studies were conducted in order to determine the combined effects of low environmental pH and temperature on embryonic survival capacity and metabolic rates in the dragonfly, Anax junius Drury. Studies were also conducted to assess the effects of hypoxia on hatching success as well as to investigate the role of hypoxia as a possible physiological triggering mechanism for hatching.
• 2.2. At water temperatures of 10–30°C, an environmental pH value of 3.0 was extremely limiting and significantly reduced hatching success.
• 3.3. Over a pH range of 3.0–5.0, a water temperature of 30°C was found to be severely limiting. Over a pH range of 6.0–7.0, hatching success was greater than 80% at test temperatures ranging from 10 to 25°C.
• 4.4. Embryos of A. junius exhibited a greater tolerance to markedly low environmental pH (3.0) than that previously reported for fish and amphibians, although survival capacity was less than 10%.
• 5.5. An environmental pH value of 3.0 has a significant detrimental effect on embryonic development. Survivorship and developmental rate increase significantly over a pH range of 4.0–5.0.
• 6.6. Oxygen consumption rates were lowest for fertilized eggs exposed to a pH of 3.0 at all test temperatures (10–30°C). Metabolic rates increased significantly at pH 4.O.
• 7.7. Embryos hatch successfully under hypoxic conditions in both aqueous and nonaqueous media. Results suggest that hypoxia acts as a triggering mechanism for hatching in this aquatic insect.

     

The development of thermoregulation in the rat kangaroo,Potorous tridactylus

• 1.1. The young were first seen out of the pouch on day 103.2 ±2.0 post-partum, and were permanently out of the pouch on day 119.7 ± 1.6, several days prior to the birth of the next young on day 122.8 ± 2.2.
• 2.2. The average mother's pouch temperature and the young's rectal temperature while in the pouch showed similar ranges—however, further analysis demonstrated that the pouch temperature decreased towards the end of lactation.
• 3.3. The difference in rectal temperature of the young in the pouch from 90–107 days to 108–123 days was 0.01 ± 0.34°C, whereas the mother's pouch temperature decreased 0.68 ± 0.37°C.
• 4.4. The results of this study suggests that curiosity and the need for solid food are the primary reasons for the young leaving the pouch and temperature does not play a primary role in the evacuation of the pouch.

     

The digestive enzymes of the pacific brown shrimp Penaeus californiensis.: I—Properties of amylase activity in the digestive tract

• 1.1. Crude extract of the whole digestive tract from the brown shrimp (P. californiensis) was investigated for digestive amylase activity.
• 2.2. Considerable amylase activity was found at pH 6.5–8.0, with optimum pH at around 7.5.
• 3.3. Optimum temperature was found between 30–40°C, similar to amylases from other crustaceans.
• 4.4. Amylase activity was highly halotolerant, having 50% maximum activity at 3 M NaCl.
• 5.5. Maximum amylase activity was found at 0.01 M NaCl.
• 6.6. Amylase activity was partially inhibited by the divalent ions Hg²⁺, Zn²⁺, Cu²⁺ and Cr²⁺.
• 7.7. Mg²⁺ and Ca²⁺ ions seemed to enhance amylase activity.