Antennal warm and cold receptors of the cave beetle,Speophyes lucidulus delar., in sensilla with a lamellated dendrite

Summary Electrophysiological examination of the 2 black-hair sensilla on the antennae of both larval stages of the cave beetle,Speophyes lucidulus, has revealed in each a pair of antagonistic thermal receptors (Fig. 1). Each sensillum was known to house the dendrites of 2 sensory cells which are associated with the extensively lamellated dendrite of a third (Corbière-Tichané 1971). One unit, a cold receptor, responds to temperature drops of 1 to 7 °C from initial temperatures between 9 and 14 °C with impulse frequencies up to 200 imp/s (Figs. 3, 4). Its antagonist, encountered less than 10% as often, is a warm receptor which responds with similar impulse frequencies to rapid rises in temperature from the same 9–14 °C (Figs. 3, 6). As indicated by the average gain of 24 imp/s for an increase of 1 °C in temperature drop, the cold unit appears almost twice as sensitive to sudden temperature change as the warm unit (14 (imp/s) °C). Examination of response scatter indicates that the average cold unit should on the basis of a single pair of responses be able to designate the greater of two temperature drops between 1 and 7 °C with 90% probability when they differ by 0.7 °C (Fig. 5). Though not yet definitive, evidence is accumulating that the third physiological unit is a dry air receptor.Abbreviations F impulse frequency in imp/s - Fc F as calculated - Fm F as measured - imp impulses - Pw partial pressure of water vapor in air - Ps saturation pressure of water vapor - r regression coefficient - T temperature - difference in Supported by the Deutsche Forschungsgemeinschaft, Sonder forschungsbereich 4, Projekt DThe authors wish to express their indebtedness to Dr. Renate Beinhauer, Faculty of Natural Sciences I — Mathematics, Univ. of Regensburg, for her help in applying statistical methods in determining resolving power.     

Response characteristics of a cold receptor in the stick insectCarausius morosus

Summary The cold cell in the easily identified mound-shaped sensillum on the 12th segment ofCarausius morosus' antennae responds to downward temperature (T) steps from about 15 °C with a sharp rise in impulse frequency (F). Responses to similar steps from higher initial temperatures are smaller (Figs. 1, 3, 4). As initialT increases from 16 °C to 31 °C, differential sensitivity to downward steps falls off by a factor of 27: to yield an average increase inF of 1 imp/s, steps down from 31 °C must increase by 1.7 °C; steps down from 16 °C, by only 0.06 °C (Fig. 5). Resolving power forT-steps at mid-range initial temperatures is about 0.7 °C, i.e. the probability that a single cold cell at average differential sensitivity will correctly discriminate between twoT steps 0.7 °C apart is 90% when the cell is presented with each step just once.The same cold cell also displays a clear dependence on steadyt between 14 °C and 24 °C (Figs. 7, 8). The static discharge rate of a single cell at average differential sensitivity has a resolving power of about 0.9 °C for steadyT. — The static discharge is not affected by the amount of water vapor in the stimulating air (Fig. 9).Abbreviations F impulse frequency in impulses per second (imp/s) - Pw partial pressure of water vapor in torr - r correlation coefficient - T temperature in °C - T step change inT     

Response characteristics of cold cell on the antenna ofLocusta migratoria L.

Summary The dendritic outer segment of the cell which is most likely the cold unit in the poreless coeloconic sensilla onLocusta migratoria antennae, has finger-like projections up to 1.5 m long and 0.13 m thick (Fig. 1). This unit responds to constant temperature, to slowly changing temperature and to step changes. Under stationary conditions impulse frequency attained 35 imp/s. Between 14 °C and 41 °C the higher frequencies were associated with the higher temperatures (Fig. 5). In this range the differential sensitivity is positive but not large: + 0.8 (imp/s)/°C. Its resolving power for steady temperature is 4.7 °C.Downward step changes produced by shifting between airstreams at different temperatures yield far higher frequencies (Figs. 2, 3). Step amplitudes were between –0.1 °C and –12 °C; the conditioning temperature from which the steps were initiated, was between 16 °C and 33 °C. Frequency peaked during the first 50 ms after stimulus onset (Fig. 2) and reached its highest values (310–340 imp/s) at initial temperatures above 30 °C and steps larger than –10 °C (Fig. 4). The mean differential sensitivity from 23 curves was –19 (imp/s)/°C and the resolving power 0.6 °C.During slowly changing temperature the impulse frequency was governed by two parameters simultaneously: ambient temperature and its rate of change. Rates were between 0.001 °C/s or less, and 0.03 °C/s in either direction. Frequency was higher during slow cooling at a given temperature than during slow warming (Fig. 6). The average differential sensitivity to the rate of change was –210 (imp/s)/(°C/s). Further, the larger responses to cooling developed at lower ambient temperatures (differential sensitivity: –1.0 (imp/s)/°C). It is to be noted that this sign is negative, in contrast to the sign for differential sensitivity to constant temperature and also for the influence of initial temperature on the response to downward step changes.Abbreviations b Slope of characteristic curve, differential sensitivity - F impulse frequency in imp/s - imp/s impulses/s - P _w partial pressure of water vapor in torr - r correlation coefficient - T temperature in °C - T T-step - x resolving power in °C     

Response of antennal cold receptors of the catopid beetles,Speophyes lucidulus Delar. andCholera angustata Fab. to very slowly changing temperature

Summary The antennal cold cells in larval black-hair sensilla of the cave beetle,Speophyes lucidulus Delar., clearly respond to rates of temperature change 5 to 10 times lower than any tested on insect cold cells so far: often below 0.0005° C/s or 2° C/h. At a given ambient temperature between 11° C and 15° C, cold-cell impulse frequency was higher when temperature was falling at these rates than when it was rising at them in every one of the twelve cells examined. The mean differential sensitivity to the rate of change was -3340±1071 (imp/s)/(° C/s), in each case two to 5 times greater (sign ignored) than in any cold cell observed previously (Loftus 1969; Corbière-Tichané and Loftus 1983). The differential sensitivity to ambient temperature,-6.8 (imp/s)/° C, was statistically indistinguishable, on the other hand, from the earlier values forSpeophyes.Antennal cold cells of six first-stage larvae of another Catopid beetle,Choleva angustata Fab., displayed very similar responses to the same stimuli. Its mean differential sensitivities were -8.1+3.9 (imp/s)/° C to ambient temperature and-3790+2190 (imp/s)/(° C/s) to the rate of temperature change. UnlikeSpeophyes this beetle spends only part of its life cycle in caves.Abbreviations dT/dt rate of temperature change in °C/s - F impulse frequency in impulses/s (imp/s) - T temperature in ° C To Sylvie Deleurance, a helpful friend who dedicated much of her life to the study of cave insects     

Effects of temperature on the properties of primary auditory fibres of the spectacled caiman,Caiman crocodilus (L.)

Summary The effect of temperature on the response properties of primary auditory fibres in caiman was studied. The head temperature was varied over the range of 10–35 ° C while the body was kept at a standard temperature of 27 °C (T_s). The temperature effects observed on auditory afferents were fully reversible. Below 11 °C the neural firing ceased.The mean spontaneous firing rate increased nearly linearly with temperature. The slopes in different fibres ranged from 0.2–3.5 imp s^–1 °C^–1. A bimodal distribution of mean spontaneous firing rate was found (<20 imp s^–1 and >20 imp s^–1 at T_s) at all temperatures.The frequency-intensity response area of the primary fibres shifted uniformly with temperature. The characteristic frequency (CF) increased nearly linearly with temperature. The slopes in different fibres ranged from 3–90 Hz °C^–1. Expressed in octaves the CF-change varied in each fibre from about O.14oct °C^–1 at 15 °C to about 0.06 oct °C^–1 at 30 °C, irrespective of the fibre's CF at T_s. Thresholds were lowest near T_s. Below T_s the thresholds decreased on average by 2dB°C^–1, above T_s the thresholds rose rapidly with temperature. The sharpness of tuning (Q_10db) showed no major change in the temperature range tested.Comparison of these findings with those from other lower vertebrates and from mammals shows that only mammalian auditory afferents do not shift their CF with temperature, suggesting that a fundamental difference in mammalian and submammalian tuning mechanisms exists. This does not necessarily imply that there is a single unifying tuning mechanism for all mammals and another one for non-mammals.Abbreviations BF best frequency: frequency of maximal response at an intensity 10 dB above the CF-threshold - CF characteristic frequency - FTC frequency threshold curve, tuning curve - T _s standard temperature of 27 °C     

Thermoregulatory responses to egg cooling in incubating bantam hens

Summary O₂ consumption, electromyographic activity (EMG), heart rate (HR), cloacal temperature (T _b) and broodpatch temperature (T _sb) were measured in bantam hens incubating eggs of different temperatures (T _e). For comparison, the metabolic response to low ambient temperature (T _a) was measured in non-incubating hens.O₂ consumption increased nearly linearly with decreasingT _e down to 30°C. At this temperature O₂ consumption was about 3.5 x the resting level. Below 30°C O₂ consumption increased non-linearly, and reached 4.6 x the resting consumption at 15°C. Eggs of 10 and 0°C gave no further increase. Pectoral muscle EMG and HR also increased in response to egg cooling. The onset of egg cooling was associated with a decrease inT _b andT _sb. Hens exposed to lowT _a showed a lower critical temperature of about 24°C.It is concluded that heat loss from the brood-patch during incubation of cold eggs is compensated by shivering thermogenesis. AtT _e below 15°C heat production is at a maximum level, corresponding to the expected O₂ consumption at exposure to an ambient temperature of –65°C.Abbrevations EMG electromyography - T _a ambient temperature - T _b cloacal temperature - T _e egg temperature - T _sb brood-patch skin temperature     

Influence of increased catecholamine levels in blood plasma during cold-adaptation and intramuscular infusion on thresholds of thermoregulatory reactions in guinea-pigs

Summary Catecholamines and some of their metabolites were determined in urine and blood plasma of guinea-pigs before, during and after acclimation to a cold or warm environment. During adaptation to 5°C the amounts of noradrenaline in plasma and 24-h urine samples continuously increased up to 600% compared with values obtained at an ambient temperature of 22°C. Higher levels of dihydroxyphenylglycol and 3-methoxy-4-hydroxyphenylglycol further indicated an increased turnover of noradrenaline during cold adaptation. Acclimation to an ambient temperature of 28°C reduced the peripheral release of noradrenaline in comparison to the release observed at 22°C. Cold-induced increases in metabolic rate and electrical muscle activity both occur at a considerably lower mean body temperature in cold-than in warm-adapted guinea-pigs. The shift of thermoregulatory cold defence reactions to a lower mean body temperature could also be observed in warm-adapted animals after intramuscular infusion of noradrenaline in amounts comparable to those released during cold adaptation.It is concluded that high peripheral sympathetic activity directly or indirectly inhibits noradrenergic neurons in the lower brain stem that modulate the thermoregulatory control system by means of their afferents to the hypothalamus. As a consequence of this peripheral influence the thermoregulatory set point is shifted to a lower mean body temperature.Abbreviations A adrenaline - CA cold adapted - CNS central nervous system - DHPG dihydroxyphenylglycol - EMA electrical muscle activity - HPLC high performance liquid chromatography - 5-HT 5-hydroxytryptamine (serotonine) - MHPG 3-methoxy-4-hydroxypheyylglycol - MR metabolic rate - NA noradrenaline - T _b mean body temperature - WA warm adapted     

Analysis of the electrical responses of antennal thermo- and hygroreceptors of Antheraea (Saturniidae,Lepidoptera) to thermal,mechanical, and electrical stimuli

Summary Antennal styloconic thermo-hygro sensilla of Antheraea were studied with DC-coupled transepithelial recordings. — The transepithelial voltage changed by about 2 mV · °C^–1. The spike frequency of the cold cell reached 300 Hz at the onset of negative temperature steps, but only 30 Hz at static temperatures (as with metal electrodes). The cold cell spikes showed a brief afterhyperpolarization that increased with temperature. The spikes of the cold- and warm-stimulated cells facilitated each other at low temperature. Mechanical stimuli (push against the sensillum, hydrostatic pressure of < ± 50 kPa, ultrasonic vibrations 120 kHz) modified the responses of the cold- and the warm-stimulated cells. Latency of cold cell responses to ultrasonic stimulation was occasionally less than 3 ms. — The impulse frequencies of the warm and the cold cells depend on the temperature and the magnitude of temperature change. When the firing rate is high enough by either or both of these parameters, it can be forced still higher by application of clamp current (outside positive). The higher the firing rate prior to clamping, the greater the effect of the current. — By analogy with sensilla for other modalities, this relationship between frequency and clamp current strongly suggests that stimulus-dependent changes in the conductance of dendritic membranes control the excitation of the warm and cold cells.Abbreviations DC direct voltage - TER transepithelial slope resistance between recording electrode and reference electrode in the hemolymph - NTC thermistor with negative temperature coefficient - TEV transepithelial voltage between electrodes - THS thermo-hygro sensillum     

Switching off the heater: influence of ambient temperature on thermoregulation by eastern skunk cabbage Symplocarpus foetidus

The protogynous inflorescences of eastern skunk cabbage, Symplocarpus foetidus, are thermogenic and regulate spadix temperature (Ts) well above ambient temperature (Ta). Continuous records of oxygen consumption, carbon dioxide production, and temperatures of plants were made at a field site in Canada. At Ta between 3-24C, Ts ranged between 16-26C, and the warmest inflorescences were those in the receptive female or early pollen-bearing stages. Respiratory rates of the 2-g spadices increased with declining Ta, and reached a maximum of 0.54 mol O2s^-1 (0.73 ml min^-1), equivalent to 0.26 W of heat production. At Ta below 3°C, several inflorescences failed to maintain high Ts and abruptly switched Ts to near freezing. Some froze when Ta dropped to about -10°C. Those that did not freeze could quickly switch to the warm state if Ta rose above about 3°C. Switching was related to the balance between heat production and heat loss that tended to produce stable equilibria at either high or low Ts. Switching between warm and cool states resulted in a bimodal distribution of Ts in the field. A respiratory quotient of 1.0 showed that carbohydrate was the substrate for thermogenesis, and bomb calorimetry of florets confirmed that energy was imported from the root. Only 11 invertebrates, including only one flying insect, were found in 195 inflorescences, suggesting that heat production and temperature regulation are not closely associated with cross-pollination.     

Genetic divergence of heat production within and between the wild progenitors of wheat and barley: evolutionary and agronomical implications

Summary We compared and contrasted calorimetrically heat production in seedlings incubated at 5°C and 24°C using genotypes from cold and warm Israeli populations of the wild progenitors of barley (Hordeum spontaneum) and wheat (Triticum dicoccoides). The wild barley sample comprised 14 accessions, 7 from cold localities and 7 from warm localities. The wild emmer wheat sample consisted of 12 accessions, 6 from a cold locality, and 6 from a warm locality. Our results indicated that (1) heat production was significantly higher in the two wild cereals at 5 °C than at 24 °C; (2) interspecifically, wild barley generates significantly more heat than wild wheat at both 5 °C and 24 °C; (3) intraspecifically, wild barley from warm environments generates significantly more heat than wild barley from cold ones, at 24 °C. We hypothesize that both the inter- and intraspecific differences in heat production evolved adaptively by natural selection in accordance with the niche-width genetic variation hypothesis. These differences presumably enhance biochemical processes, hence growth, thereby leading to the shorter annual cycle of barley compared to that of wheat, and may explain the wider range of the wild and cultivated gene pools of barley, as compared with those of wheat. We propose that a shortening of the growth period through utilizing heat production gene(s) is feasible by classical methods of breeding and/or modern biotechnology.     

Seasonal control of energy requirements for thermoregulation in the djungarian hamster (Phodopus sungorus), living in natural photoperiod

Summary Djungarian dwarf hamsters,Phodopus s. sungorus, were kept in natural photoperiodic conditions throughout the year, either inside at a constantT _a of 23°C or outside subjected to seasonally varyingT _a. Comparisons were made between hamsters from both conditions to evaluate the significance of seasonal changes in photoperiod and/orT _a as environmental cues for seasonal acclimatization inPhodopus. Basal metabolic rate was lowest in July (1.68 ml/g·h) and highest in January (2.06 ml/g·h inPhodopus living outside), combined with a decrease inT _1c from 26°C in July to 20°C in January. This was parallelled by seasonal changes in body weight (summer 42 g, winter 25g), fur colouration, fur depth and the occurrence of short daily torpor.AtT _a below thermoneutrality total energy requirements for thermoregulation in winter acclimatizedPhodopus were found 36% lower than summer values (e.g. at O°CT _a in summer 1,160 mW, in winter 760 mW), which were effected by a combined strategy of reducing body weight (19%) together with improvements of thermal insulation of the body surface (17%). All seasonal changes were similar inPhodopus living inside or outside, suggesting that seasonal changes in photoperiod and not seasonal changes inT _a is the overriding controller for the environmental cueing of seasonality in energy requirements for thermoregulation.This research was supported by the Deutsche Forschungsgemeinschaft (He 990)     

Thermal acclimation induced compensation in biochemical constituents of the Indian freshwater leech,Poecilobdella viridis (Blanchard)

Poecilobdella viridis was used to study the variations in the biochemical parameters: body protein, glycogen and water, following warm (32.0° ± 0.5°C) and cold (10.0° ± 0.5°C) acclimation for 5, 10, 15 and 30 days. The percentage of glycogen decreased significantly (p < 0.05) during both warm and cold acclimation whereas the protein percentage increased significantly (p < 0.05). The percentage of water was significantly (p < 0.05). reduced during both acclimation processes. Ecophysiological significance of these alterations to leeches, in counteracting the ambient thermal fluxes, has been briefly discussed.     

The effects of warming by active and passive means on the subsequent responses to cold water immersion

Two experiments were undertaken to investigate the effects of warming the body upon the responses during a subsequent cold water immersion (CWI). In both experiments the subjects, wearing swimming costumes, undertook two 45-min CWIs in water at 15° C. In experiment 1, 12 subjects exercised on a cycle ergometer until their rectal temperatures (T _re) rose by an average of 0.73°C. They were then immediately immersed in the cold water. Before their other CWI they rested seated on a cycle ergometer (control condition). In experiment 2, 16 different subjects were immersed in a hot bath (40° C) until their T _re rose by an average of 0.9° C; they were then immediately immersed in the cold water. Before their other CWI they were immersed in thermoneutral water (35° C; control condition). Heart rate in both experiments and respiratory frequency in experiment 1 were significantly (P < 0.05) higher during the first 30 s of CWI following active warming. In experiment 1, the rate of fall of T _re during the final 15 min of CWI was significantly (P < 0.01) faster when CWI followed active warming (2.46° C · h^–1) compared with the control condition (1.68°C · h^–1). However, this rate was observed when absolute T _re was still above that seen in the control CWIs. It is possible, therefore, that if longer CWIs had been undertaken, the two temperature curves may have converged and thereafter fallen at similar rates; this was the case with the aural temperature (T _au) seen in experiment 1 and the T _au and T _re in experiment 2. It is concluded that pre-warming is neither beneficial nor detrimental to survival prospects during a subsequent CWI.     

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.     

Energy metabolism,body-temperature and breathing parameters in nontorpid blue-naped mousebirdsUrocolius macrourus

Summary Breathing frequencyF _r of resting blue-naped mousebirdsUrocolius macrourus lies between 50–70 per min and correlates directly with ambient temperatureT _a and energy metabolismM. The nocturnal mean energy intake per breath varies between 5.6–17.7 mJ/g. At highT _a the birds show gular fluttering with a relatively constantF _r of about 460 min^–1.M shows a constant absolute day-night difference of 25 J/g·h; the relative differences areT _a-dependent between 36–168% (lower values at lowerT _a). Thermal conductance is 2.10–2.15 J/g·h·°C (predicted 2.67), indicating a good insulation. Basal metabolic rate BMR is reduced by 63% compared to predicted values. At aT _a-range of +8–36 °C the birds are normothermic. Below this range nocturnalT _b andM decrease slightly with fallingT _a. The birds show partial heterothermia (shallow hypothermia). Clustering is an effective energy saving strategy which allows loweringM with keeping highT _b even at lowT _a.Oxygen-intake is controlled byF _r as well as by tidal volumeV t inT _a-dependent changing portions.V T can vary between 0.29–0.91 ml (mean value 49.7 ml).Abbreviations T _a ambient temperature - T _b body temperature - M energy metabolism - F _r breathing frequency - V T tidal volume - BMR basal metabolic rate - TNP thermoneutral point     

Evaporative cooling and endothermy in the 13-year periodical cicada,Magicicada tredecem (Homoptera: Cicadidae)

Summary The thermobiology of a cicada, Magicicada tredecem, from a warm, high humidity environment was investigated. Thoracic temperature (T_th) of M. tredecem in the field was strongly dependent on, and consistently higher than, ambient temperature (T_am), averaging 33.0±0.19°C on warm sunny days (T_am=28–29°C, rh=60–75%). Laboratory studies documented cuticle water fluxes high enough ( 5mg · cm^–2 · h^–1 in dry air at 40°C) to result in a significant degree of passive evaporative cooling, but the ability of M. tredecem to actively facilitate evaporative water loss during thermal stress is comparatively limited: water loss rates (WLR) of live M. tredecem at 40°C (dry air) were only 35–45% greater than those of dead cicadas. The limited ability of M. tredecem to facilitate transcuticular WLR is associated with limited surface distribution of the cuticular ducts through which water is actively extruded during evaporative cooling. In the laboratory, active extrusion of water had no appreciable effect on T_th, demonstrating that evaporative cooling was due largely to passive water flux through the highly permeable cuticle. The location of the abdominal pore tracts is such that extrusion of water through the ducts may preferentially cool the heart and perhaps other abdominal tissues. Long-term climatological data indicate that M. tredecem rarely encounters T_am levels high enough (i.e., above its apparent T_th setpoint of 34–35°C) to require evaporative cooling. Inactive M. tredecem can endothermically increase T_th. An hypothesis is proposed to account for the diversity of body temperature setpoints in cicadas.Abbreviations rh relative humidity - SOT standard operating temperature - T _am ambient temperature - T _b body temperature - T _sp body temperature setpoint - T _th thoracic temperature - TWF transcuticular water flux - WLR water loss rate     

Effect of ambient temperature and E. coli endotoxin upon the plasma iron level in wild house mice in winter season

Summary The effects of ambient temperatures of 10°C and 30°C and of E. coli endotoxin on brain temperature and plasma iron level were investigated in unrestrained wild house mice, Mus musculus. In control animals (i.p. saline-injected) exposed to cold environmenta the brain temperature decreased and plasma iron levels were lower than those observed under thermoneutral conditions (30°C). Animals injected i.p. with endotoxin (0.5 g·kg^-1) and placed at 30°C showed a drop in plasma iron level during the fever episode. The results provide strong evidence for a relationship between brain temperature and plasma iron level in control mice under thermoneutral conditions, and show that during cold exposure or after injection of endotoxin, there is no linear correlation between brain temperature and plasma iron. Moreover, it was found that cold stress influences plasma iron level and that this influence is not mediated by changes in brain temperature.Abbreviations EP endotoxin pyrogen - T _A ambient temperature - T _Br brain temperature - T _Br change in T _Br in relation to its initial value in feverish or control mice - T _Br difference between T _Br in feverish and control mice     

Aerobic mitochondrial capacities in Antarctic and temperate eelpout (Zoarcidae) subjected to warm versus cold acclimation

Capacities and effects of cold or warm acclimation were investigated in two zoarcid species from the North Sea (Zoarces viviparus) and the Antarctic (Pachycara brachycephalum) by investigating temperature dependent mitochondrial respiration and activities of citrate synthase (CS) and NADP⁺ -dependent isocitrate dehydrogenase (IDH) in the liver. Antarctic eelpout were acclimated to 5°C and 0°C (controls) for at least 10 months, whereas boreal eelpout, Z. viviparus (North Sea) were acclimated to 5°C and to 10°C (controls). Liver sizes were found to be increased in both species in the cold, with a concomitant rise in liver mitochondrial protein content. As a result, total liver state III rates were elevated in both cold-versus and warm-exposed P. brachycephalum and Z. viviparus, with the highest rates in boreal eelpout acclimated to 5°C. CS and IDH activities in the total liver were similar in Z. viviparus acclimated to 5°C and 10°C, but decreased in those warm acclimated versus control P. brachycephalum. Enzyme capacities in the total liver were higher in eelpout from Antarctica than those from the North Sea. In conclusion, cold compensation of aerobic capacities in the liver seems to be linked to an increase in organ size with unchanged specific mitochondrial protein content. Despite its life in permanently cold climate, P. brachycephalum was able to reduce liver aerobic capacities in warm climate and thus, displayed a capacity for temperature acclimation.     

Cold-induced changes in brown adipose tissue thermogenic capacity of immunocompetent and immunodeficient hairless mice

Mild cold acclimation (22°C, 3 weeks) of hairless mice was shown to increase 5-fold the brown adipose tissue uncoupling protein content in immunodeficient BALB/c nu/nu mice, but by only 2.3-fold in immunocompetent BFU mice. The difference in activation of brown adipose tissue thermogenic capacity was due to a 2-fold increase in the content of brown adipose tissue in nu/nu mice only, which was paralleled by an increase in brown adipose tissue protein but not DNA content. Likewise, only in nu/nu mice the cold acclimation increased the reaction of natural killer cells in blood and peritoneal exudate with a shift from spleen to lymph nodes and increased the phagocytic index. The results indicate that the immune system may influence the defence against cold at the level of brown adipose tissue thermogenesis.Abbreviations AU arbitrary unit(s) - bw body weight - HEMA 2-hydromethyl-metacrylate copolymer - BAT brown adipose tissue - UCP uncoupling protein - ATPase mitochondrial F_oF₁-ATPsynthase - IL-1 interleukin 1 - TNF tumour necrosis factor - NK cells natural killer cells - T _a ambient temperature     

Effects of temperan a central synapse between identified motor neurons in the locust

Summary Changing the temperature from 10–40 °C modifies the transmission at an established monosynaptic connection between the fast extensor tibiae (FETi) and flexor tibiae motor neurons in the metathoracic ganglion of the locustSchistocerca gregaria (Forskål). Striking changes occur to the shape of the spikes, to membrane resistance, to the synaptic delay, and to the evoked synaptic potentials.In the presynaptic FETi motor neuron, raising the temperature reduces the amplitude of an antidromic spike recorded in the soma by a factor of 10 (40 mV to 4 mV), reduces the time taken to reach peak amplitude by 5 (3.5 to 0.7 ms) and decreases the duration at half maximum amplitude by 0.5. The conduction velocity of the spike in the axon is increased by 50% from 10 °C to 40 °C. Orthodromic spikes are affected by temperature in a similar way to the antidromic spikes.The membrane resistance of both pre- and postsynaptic motor neurons falls as the temperature is raised. The membrane resistance of FETi falls by a factor of 4 (about 4 M at 10 °C to 1 M at 40 °C). A contributory component to this fall could be the increase in the frequency of synaptic potentials generated as a result of inputs from other neurons. No temperature dependence could be demonstrated on the voltage threshold relative to resting potential for evoking orthodromic spikes, but because the resistance changes, the current needed to achieve this voltage must be increased at higher temperatures.The latency measured from the peak of the spike in the soma of FETi to the start of the EPSP in the soma of a flexor motor neuron decreases by a factor of 20 (10 ms at 10 °C to 0.5 ms at 40 °C).In a postsynaptic flexor tibiae motor neuron, the amplitude of the evoked synaptic potential increases by a factor of 3.4 (5 mV to 17 mV), its duration at half maximum amplitude decreases by 3 (7 ms at 12 °C to 2.3 ms at 32 °C) and its rate of rise increases by 3. An increased likelihood that spikes will occur in the flexor contributes to the enhanced amplitude of the compound EPSP at temperatures above 20 °C.Abbreviation FETi fast extensor tibiae motor neuron