Ventilation and gas exchange during rest and exercise in adult green sea turtles

Summary Ventilation and metabolic rate were measured during exercise in adult female green turtles at Tortuguero, Costa Rica. Six turtles were studied at night on the beach while actively covering their nests. Five turtles, captured after nesting, were studied at rest, during 20 min of spontaneous activity, and during recovery from the activity. Arterial blood samples were obtained from the latter animals and analyzed for pH, , O₂ concentration and lactate concentration. Blood was obtained by heart puncture from 8 turtles immediately after nesting and analyzed for blood lactate. Active metabolism ( ) in both groups was almost 10 times the standard resting value (0.024 l/kg·h). The increase in ventilation during exercise, due exclusively to higher breathing frequency, exceeded the increase in , so that the ratio (the air convection requirement), more than doubled. The respiratory exchange ratio, , that averaged 0.56 in the resting turtles, increased to 1.08 during exercise in the captured turtles and was 0.90 in the nesting animals. Arterial and O₂ saturation remained unchanged during exercise, indicating efficient gas exchange in the lungs. Pre-exercise values of all variables were restored 1 h after the end of exercise. Blood acid-base changes associated with activity in the captive turtles were variable and not statistically significant, but suggested partially compensated metabolic acidosis. Lactate concentrations were significantly elevated in the nesting turtles.     

Resting metabolic rates in boid snakes: allometric relationships and temperature effects

Summary Resting metabolic rates (RMR) of 34 species from 18 genera of boas and pythons (Serpentes: Boidae), with body masses ranging from 2 to 67,800 g, were determined as oxygen consumption ( ) and carbon dioxide production ( ) at three ambient temperatures (T _a).The temperature coefficient of metabolism (Q₁₀) averaged 2.61 betweenT _a of 20–30°C and 2.65 between 30 and 34°C. The respiratory exchange ratio RE (= / ) increased slightly with increasingT _a (0.795 at 20°C, 0.819 at 30°C, and 0.834 at 34°C). Interspecific differences in Q₁₀ and RE were slight or insignificant.A multiple regression relating metabolism ( ) to mass andT _a explained 97% of the variance in the pooled interspecific data. The mass exponent was 0.806, which is approximately the same as reported for squamates and for all reptilian taxa combined. The mean within-species slope (0.732) was significantly less than the slope for pooled data, but did not differ significantly from 0.75. In 40 of 42 cases (14 species at 3T _a), within-species slopes did not differ from each other. Values of the adjusted mean Y, from covariance analysis, were significantly and positively correlated with mass, indicating that the mass coefficient increases with increasing mass.Considerable variation in metabolic rate is apparent both within and between ecological and taxonomic categories.Original metabolic data are available from the National Auxiliary Publications Services, c/o Microfiche Publication, P.O. Box 3153 Grand Central Station, New York, New York 10017, USA     

Effects of temperature and altitude on ventilation and gas exchange in chukars (Alectoris chukar)

Summary The effects of ambient temperature (T _a) on ventilation and gas exchange in chukar partridges (Alectoris chukar) were determined after acclimation to low and high altitute (LA and HA; 340 and 3,800 m, respectively).At both LA and HA, oxygen consumption ( ) increased with decreasingT _a atT _a from 20 to –20°C. AtT _a of 35 to 40°C, increased above thermoneutral values at HA but remained constant and minimal at LA. Water loss rates increased rapidly atT _a>30°C at both altitudes as birds began to pant. Ventilation rates (f) during panting were 5-to 23-fold greater than the minimalf at thermoneutralT _a.Increased atT _a below thermoneutrality was supported by increased minute volume (V i) at both altitudes. The change inV i was primarily a function of changing tidal volume (V t), althoughf increased slightly asT _a declined. Oxygen extraction ( ) remained fairly constant atT _a below 20°C at both altitudes. BothV t and were considerably lower when birds were panting than at lowerT _a.Chukars showed few obvious ventilatory adaptations to HA. The 35% change in between 340 and 3,800 m was accommodated by a corresponding change inV i (btps), most of which was accomplished by increasedf at HA, along with a slight increase in .Abbreviations and symbols HA high altitude - LA low altitude - rate of evaporative water loss - oxygen extraction efficiency - f respiratory frequency - V t tidal volume - V i minute volume - BMR basal metabolic rate - MHP metabolic heat production     

Effect of venous (gut) CO2 loading on intrapulmonary gas fractions and ventilation in the tegu lizard

Summary Studies were conducted to determine regional pulmonary gas concentrations in the tegu lizard lung. Additionally, changes in pulmonary gas concentrations and ventilatory patterns caused by elevating venous levels of CO₂ by gut infusion were measured.It was found that significant stratification of lung gases was present in the tegu and that dynamic fluctuations of CO₂ concentration varied throughout the length of the lung. Mean was greater and less in the posterior regions of the lung. In the posterior regions gas concentrations remained nearly constant, whereas in the anterior regions large swings were observed with each breath. In the most anterior sections of the lung near the bronchi, CO₂ and O₂ concentrations approached atmospheric levels during inspiration and posterior lung levels during expiration.During gut loading of CO₂, the rate of rise of CO₂ during the breathing pause increased. The mean level of CO₂ also increased. Breathing rate and tidal volume increased to produce a doubling ofV _E.These results indicate that the method of introduction of CO₂ into the tegu respiratory system determines the ventilatory response. If the CO₂ is introduced into the venous blood a dramatic increase in ventilation is observed. If the CO₂ is introduced into the inspired air a significant decrease in ventilation is produced. The changes in pulmonary CO₂ environment caused by inspiratory CO₂ loading are different from those caused by venous CO₂ loading. We hypothesize that the differences in pulmonary CO₂ environment caused by either inspiratory CO₂ loading or fluctuations in venous CO₂ concentration act differently on the IPC. The differing response of the IPC to the two methods of CO₂ loading is the cause of the opposite ventilatory response seen during either venous or inspiratory loading.Abbreviations IPC intrapulmonary chemoreceptors - UAC upper airway chemoreceptors - V _T inspiratory tidal volume - CO₂ gas fraction - O₂ gas fraction - V _E minute ventilation     

Respiratory gas exchange during thermogenesis inPhilodendron selloum Koch

During peak thermogenesis of anthesis, high rates of respiration by the sterile male florets on the spadix ofPhilodendron selloum significantly reduce the oxygen tension (P_{O 2}) and raise CO₂ tension between the florets. Nevertheless, respiration is not limited by the availability of O₂ under natural conditions. At experimental P_{O 2} below about 17 kPa, however, florets begin to show decreased O₂ consumption. A respiratory exchange ratio of 0.83 indicates that the major energy source is not starch, but is probably lipid.Abbreviations and symbols capacitance of the gas phase for O₂ (ml O₂ cm^-3 kPa^-1) - D_{O 2} binary diffusion coefficient of O₂ in air (cm² min^-1) - K_{O 2} Krogh's diffusion coefficient (ml O₂ cm^-2 min^-1 kPa^-1 cm) - P_{O 2} P_{CO 2} partial pressures of O₂ and CO₂ (kPa) - rate of O₂ consumption (ml O₂ g^-1 h^-1) - F_gas fractional gas volume - P₈₀ O₂ partial pressure at which falls below 80% of maximum - RE respiratory exchange ratio      

Aerobic metabolism of the lizardVaranus exanthematicus: Effects of activity, temperature, and size

Summary Oxygen consumption was measured at rest and during spontaneous activity at body temperatures of 25 and 35°C in 14 fasting Savanna monitor lizards,Varanus exanthematicus ranging in weight from 172 to 7500 g. The allometric relationship between metabolic rate at 25°C and body weight (W) is given by: (ml O₂ STPD·g^–1·hr^–1)=0.88W ^–0.43 (Fig. 2). Although statistical comparisons are equivocal, this intraspecific size dependence exceeds that reported for interspecific comparisons among reptiles and other vertebrate groups (Fig 3). A reproducible diurnal pattern of activity was observed in undisturbed animals with minimum values of between 2400 and 0800 h (Fig. 1). Spontaneous activity and generally reached peak values between 1200 and 2000 hrs. The average ratio of active aerobic metabolic rate (AMR) to minimum (standard) aerobic metabolic rate (SMR) was 8.2. This voluntary AMR/SMR inVaranus exceeds the AMR/SMR for most reptiles stimulated to exhaustion. The high aerobic capacity is consistent with other evidence for efficient exchange and transport of respiratory gases inV. exanthematicus; e.g., low or absent intracardiac shunt flow resulting in high arterial saturation and low ventilation and perfusion requirements.     

Effects of ambient temperature and altitude on ventilation and gas exchange in deer mice (Peromyscus maniculatus)

Summary The effects of different ambient temperatures (T _a) on gas exchange and ventilation in deer mice (Peromyscus maniculatus) were determined after acclimation to low and high altitude (340 and 3,800 m).At both low and high altitude, oxygen consumption ( ) decreased with increasingT _a atT _a from –10 to 30 °C. The was 15–20% smaller at high altitude than at low altitude atT _a below 30 °C.Increased atT _a below thermoneutrality was supported by increased minute volume ( ) at both low and high altitude. At mostT _a, the change in was primarily a function of changing respiration frequency (f); relatively little change occurred in tidal volume (V _T) or oxygen extraction efficiency (O₂EE). AtT _a=0 °C and below at high altitude, was constant due to decliningV _T and O₂EE increased in order to maintain high .At high altitude, (BTP) was 30–40% higher at a givenT _a than at low altitude, except atT _a below 10 °C. The increased at high altitude was due primarily to a proportional increase inf, which attained mean values of 450–500 breaths/min atT _a below 0 °C. The (STP) was equivalent at high and low altitude atT _a of 10 °C and above. At lowerT _a, (STPD) was larger at low altitude.At both altitudes, respiratory heat loss was a small fraction (<10%) of metabolic heat production, except at highT _a (20–30 °C).Abbreviations EHL evaporative heat loss - f respiration frequency - HL _a heat loss from warming tidal air - HL _e evaporative heat loss in tidal air - HL total respiratory heat loss - MHP metabolic heat production - O ₂ EE oxygen extraction efficiency - RQ respiratory quotient - T _a ambient temperature - T _b body temperatureT _lc lower critical temperature - carbon dioxide production - evaporative water loss - oxygen consumption - minute volume - V _T tidal volume     

Oxygen-dependence of metabolic rate in the muscles of craniates

We present evidence that oxygen consumption (V_\textO2 ) (V_{{{\text{O}}_{2} }} ) is oxygen partial pressure (P_\textO2 ) (P_{{{\text{O}}_{2} }} ) dependent in striated muscles and P_\textO2 P_{{{\text{O}}_{2} }} -independent in the vasculature in representatives of three craniate taxa: two teleost fish, a hagfish and a rat. Blood vessel V_\textO2 V_{{{\text{O}}_{2} }} displayed varying degrees of independence in a P_\textO2 P_{{{\text{O}}_{2} }} range of 15–95 mmHg, while V_\textO2 V_{{{\text{O}}_{2} }} by striated muscle tissue slices from all species related linearly to P_\textO2 P_{{{\text{O}}_{2} }} between 0 and 125 mmHg, despite V_\textO2 V_{{{\text{O}}_{2} }} rates varying greatly between species and muscle type. In salmon red muscle, lactate concentrations fell in slices incubated at a P_\textO2 P_{{{\text{O}}_{2} }} of either 30 or 100 mmHg, suggesting aerobic rather than anaerobic metabolism. Consistent with this finding, potential energy, a proxy of ATP turnover, was P_\textO2 P_{{{\text{O}}_{2} }} -dependent. Our data suggest that the reduction in V_\textO2 V_{{{\text{O}}_{2} }} with falling P_\textO2 P_{{{\text{O}}_{2} }} results in a decrease in ATP demand, suggesting that the hypoxic signal is sensed and cellular changes effected. Viability and diffusion limitation of the preparations were investigated using salmon cardiac and skeletal muscles. Following the initial P_\textO2 P_{{{\text{O}}_{2} }} depletion, reoxygenation of the Ringer bathing salmon cardiac muscle resulted in V_\textO2 \texts V_{{{\text{O}}_{2} }} {\text{s}} that was unchanged from the first run. V_\textO2 V_{{{\text{O}}_{2} }} increased in all muscles uncoupled with p-trifluoromethoxylphenyl-hydrazone (FCCP) and 2,4-dinitrophenol (DNP). Mitochondrial succinate dehydrogenase activity, quantified by reduction of 3-(4,5-dimethylthiazol)-2,5-diphenyl-2H-tetrazolium bromide (MTT) to formazan, was constant over the course of the experiment. These three findings indicate that the tissues remained viable over time and ruled out diffusion-limitation as a constraint on V_\textO2 V_{{{\text{O}}_{2} }} .     

Respiration of the air breathing fishPiabucina festae

Summary Piabucina festae, a Central American stream fish, breathes air frequently, even in air saturated water, however, is not an obligate air breather. Without access to air, it can maintain routine by aquatic respiration down to aP _wO₂ of about 70 Torr which is its critical O₂ tension (P _cO₂, Fig. 5). Aerial respiration averages 10% of total in air saturated water and 70% in hypoxic water (Fig. 4). At lowP _wO₂ air breathing is more frequent (Fig. 1), and more O₂ is utilized from each air breath (Table 3), and tidal volume may increase (Fig. 7). Vascularized respiratory compartments or cells (Fig. 6), located in the second chamber of the physostomus gas bladder, function for aerial respiration. In ventilation air is gulped and forced through a large pneumatic duct into the gas bladder, excess gas is then released through opercula. Inspiration always precedes expiration and tidal volume is small, keeping gas bladderP _{O 2} low (Table 4). Major differences in the air breathing physiology ofP. festae and other species are its higherP _cO₂, a low aerial in normoxic water, even though air gulps are frequent, and its pattern of inhalation prior to expiration. The interrelationship and optimization of the three gas bladder functions (buoyancy, sound reception, and air breathing) inP. festae is discussed. Aerial respiration may have evolved secondarily to the gas bladder's function in buoyancy control.     

Ventilation and gas exchange in the diamondback water snake,Natrix rhombifera

Summary Simultaneous measurements of pulmonary and cutaneous oxygen and carbon dioxide exchange, pulmonary ventilation and heart rate were made on the diamondback water snake,Natrix rhombifera at 28°C using body plethysmography. Resting lung volume, maximum lung volume and tracheal volume were also measured.The following mean values were measured in undisturbed snakes breathing room air: total (pulmonary and cutaneous) O₂ uptake 46 mol · (kg min)^–1; total CO₂ output, 49 mol · (kg min)^–1; tidal volume, 12 ml (BTPS) · kg^–1; ventilatory rate, 6.9 min^–1; heart rate, 42 min^–1. From the measurements of tracheal volume, the effective (alveolar) ventilation was estimated as approximately 70% of total ventilation resulting in effective pulmonary and of 130 Torr and 20 Torr respectively. Cutaneous exchange accounted for 8.1% of the total and 12.4% of the total .Resting lung volume of anaesthetized snakes was 75 ml (BTPS) · kg^–1, maximum lung volume was 341 ml (BTPS) · kg^–1 and tracheal volume was 3.9 ml (BTPS) · kg^–1.     

Respiratory responses to long-term temperature exposure in the box turtle,Terrapene ornata

Summary In late February, seven box turtles were collected with body temperatures between 7 and 9°C. Ventilation, gas exchange and end-tidal and were recorded at 5, 10, 15 and 25°C, the animals being at each temperature for 2 to 3 weeks. There was a pronounced diurnal rhythm of breathing frequency at all temperatures. At 5°C the mean 24-h frequency was only 3.7 breaths h^–1. At 15°C the frequency was 16 times higher with a 17-fold increase of ventilation. Oxygen uptake only changed from 3.4 to 12.7 ml·kg^–1·h^–1. Consequently, the ratio (ventilation, ml BTPS/O₂ uptake, ml STPD) increased from 12.5 at 5°C to 48 at 15°C, but decreased to 24 at 25°C. The decrease of this ratio during cold exposure contrasts with an increase of the ratio during cooling earlier reported for fresh water turtles,Pseudemys. Cutaneous CO₂ elimination was important at low temperature. This caused a decrease of the pulmonary gas exchange ratio so that end-tidal remained low at 5°C in spite of an end-tidal of only 54 Torr.     

Thermoregulation,gas exchange,and ventilation in Adelie penguins (Pygoscelis adeliae)

Summary Adelie penguins (Pygoscelis adeliae) experience a wide range of ambient temperatures (T _a) in their natural habitat. We examined body temperature (T _b), oxygen consumption ( ), carbon dioxide production ( ), evaporative water loss ( ), and ventilation atT _a from –20 to 30 °C. Body temperature did not change significantly between –20 and 20°C (meanT _b=39.3°C).T _b increased slightly to 40.1 °C atT _a=30°C. Both and were constant and minimal atT _a between –10 and 20°C, with only minor increases at –20 and 30°C. The minimal of adult penguins (mean mass 4.007 kg) was 0.0112 ml/[g·min], equivalent to a metabolic heat production (MHP) of 14.9 Watt. The respiratory exchange ratio was approximately 0.7 at allT _a. Values of were low at lowT _a, but increased to 0.21 g/min at 30°C, equivalent to 0.3% of body mass/h. Dry conductance increased 3.5-fold between –20 and 30°C. Evaporative heat loss (EHL) comprised about 5% of MHP at lowT _a, rising to 47% of MHP atT _a=30°C. The means of ventilation parameters (tidal volume [VT], respiration frequency [f], minute volume [I], and oxygen extraction [ ]) were fairly stable between –20 and 10°C (VT did not change significantly over the entireT _a range). However, there was considerable inter- and intra-individual variation in ventilation patterns. AtT _a=20–30°C,f increased 7-fold over the minimal value of 7.6 breaths/min, and I showed a similar change. fell from 28–35% at lowT _a to 6% atT _a=30°C.Abbreviations C thermal conductance - EHL evaporative heat loss - oxygen extraction - f respiratory frequency - MHP metabolic heat production - evaporative water loss - LCT lower critical temperature - RE respiratory exchange ratio - T _a ambient temperature - T _b body temperature - rate of oxygen consumption - rate of carbon dioxide production - I inspiratory minute volume - VT tidal volume     

Altitudinal and seasonal effects on aerobic metabolism of deer mice

Summary I compared the maximal aerobic metabolic rates ( ), field metabolic rates (FMR), aerobic reserves ( -FMR), and basal metabolic rates (BMR) of wild and recently captured deer mice from low (440 m) and high (3800 m) altitudes. To separate the effects of the thermal environment from other altitudinal effects, I examined mice from different altitudes, but similar thermal environments (i.e., summer mice from high altitude and winter mice from low altitude). When the thermal environment was similar, , FMR, and aerobic reserve of low and high altitude mice did not differ, but BMR was significantly higher at high altitude. Thus, in the absence of thermal differences, altitude had only minor effects on the aerobic metabolism of wild or recently captured deer mice.At low altitude, there was significant seasonal variation in , FMR, and aerobic reserve, but not BMR. BMR was correlated with , but not with FMR. The significant positive correlation of BMR with indicates a cost of high , because higher BMR increases food requirements and energy use during periods of thermoneutral conditions.Abbreviations BMR basal metabolic rate - FMR field metabolic rate - partial pressure of oxygen - T _a ambient temperature - T _b body temperature - T _e operative temperature - maximal aerobic metabolic rate     

Dynamics of cardiorespiratory function in Standardbred horses during different intensities of constant-load exercise

Summary Six Standardbred horses were used to evaluate the time course of pulmonary gas exchange, ventilation, heart rate (HR) and acid base balance during different intensities of constant-load treadmill exercise. Horses were exercised at approximately 50%, 75% and 100% maximum oxygen uptake ( max) for 5 min and measurements taken every 30 s throughout exercise. At all work rates, the minute ventilation, respiratory frequency and tidal volume reached steady state values by 60 s of exercise. At 100% max, the oxygen consumption ( ) increased to mean values of approximately 130 ml/kg·min, which represents a 40-fold increase above resting . At the low and moderate work rates, showed no significant change from 30 s to 300 s of exercise. At the high work rate, the mean at 30 s was 80% of the value at 300 s. The HR showed no significant change over time at the moderate work rate but differing responses at the low and high work rates. At the low work rate, the mean HR decreased from 188 beats/min at 30 s to 172 beats/min at 300 s exercise, whereas at the high work rate the mean HR increased from 204 beats/min at 30 s to 221 beats/min at 300 s exercise. No changes in acid base status occurred during exercise at the low work rate. At the moderate work rate, a mild metabolic acidosis occurred which was nonprogressive with time, whereas the high work rate resulted in a progressive metabolic acidosis with a base deficit of 16 mmol/l by 300 s exercise. It is concluded that the kinetics of gas exchange during exercise are more rapid in the horse than in man, despite the relatively greater change in in the horse when going from rest to high intensity exercise.Symbols and abbreviations E minute ventilation - V _T tidal volume - oxygen uptake - carbon dioxide output - oxygen pulse - ventilatory equivalent for oxygen - ventilatory equivalent for carbon dioxide - R respiratory exchange ratio - HR heart rate - SBC standard bicarbonate - STPD standard temperature and pressure dry - BTPS body temperature and pressure saturated - arterial oxygen content - arteriovenous oxygen content difference - Rf respiratory frequency     

Ventilation and oxygen consumption in rosy finches and house finches at sea level and high altitude

Summary Rosy finches (Leucosticte arctoa) breed at altitudes above 3500 m in eastern California. House finches (Carpodacus mexicanus) belong to the same subfamily (Carduelinae), but breed at much lower elevations. Oxygen consumption ( ) and ventilatory parameters of these two species were measured over a wide range of ambient temperatures (T _a) at low altitude (LA; 150 m) and at high altitude (HA; 3800 m).Minimal nighttime 's of rosy finches and house finches at LA (T _a=30°C) were close to allometrically predicted values for passerine birds. At both altitudes, increased linearly with decreasingT _a betweenT _a=20 and –10°C. Resting 's were slightly higher at HA than at LA on average.In both species, minute volume ( ) was inversely related toT _a.T _a-correlated increases in resulted from significant increases in both ventilatory frequency (f) and tidal volume (V T) at both altitudes. Oxygen extraction efficiency ( ) was independent ofT _a in rosy finches at LA, but declined significantly with decreasingT _a in rosy finches at HA and in house finches at both altitudes.At a givenT _a, both species had significantly greater (BTPS) at HA than at LA. Altitude-correlated increases in resulted primarly from increases inf with little change inV T. was significantly greater at HA than at LA in both species.In spite of the difference in altitudinal distributions of rosy finches and house finches, there were few conspicuous interspecific differences in metabolic or ventilatory adaptation to altitude or lowT _a over the range of conditions examined.Symbols and abbreviations BMR basal metabolic rate - BTPS at body temperature and pressure, saturated - oxygen extraction efficiency - f ventilation frequency - h mean coefficient of heat transfer - HA high altitude - instantaneous oxygen consumption - LA low altitude - RH relative humidity - SMR standard metabolic rate - STPD standard temperature and pressure, dry - T temperature - a ambient - b body - lc lower critical of thermoneutral zone - minute volume - V T tidal volume     

Metabolism,temperature relations,maternal behavior,and reproductive energetics in the ball python (Python regius)

Summary Thermogenic incubation has been documented in two large species of pythons, but the phenomenon has not been studied in small species with concomitantly large heat transfer coefficients. We describe behavior, metabolic rates, mass changes, and temperature relations for adult ball pythons (Python regius), the smallest member of the genus, during the reproductive cycle. Egg and hatchling metabolism and hatchling growth rates were also examined.Rates of oxygen consumption ( ) of both gravid and non-gravid snakes showed typical ectothermic responses to changing ambient temperature (T _a). TheQ ₁₀ forT _a's of 20–35°C was 2.2–2.3. The of gravid females was significantly greater than that of non-gravid snakes at allT _a. Maximum oxygen consumption ( max) during forced exercise was about 12 times resting atT _a=30°C.Eggs (5–6 per female) were laid in April. Total clutch mass was approximately 32% of the females' pre-oviposition mass. After oviposition, mother snakes coiled tightly around their clutches and remained in close attendance until the eggs hatched in June. Sudden decreases inT _a elicited abrupt but transient 2- to 4-fold increases in the of incubating females. Similar responses were not observed in non-incubating snakes. The steady-state of incubating females was independent ofT _a. In no case was body temperature (T _b) elevated more than a few tenths of a degree aboveT _a in steady-state conditions.The of developing eggs increased sigmoidally through the 58–70 day incubation period. Total oxygen consumption during incubation atT _a=29.2°C was about 3.61 per egg. Young snakes quadrupled their mass during their first year of growth.Compared to larger python species which are endothermic during incubation, ball pythons have similar aerobic scopes and higher mass-specific max. However, effective endothermy in ball pythons is precluded by high thermal conductance and limited energy stores.     

The variability of respiratory pattern and gas exchange

It is known, that spectral analysis of heart rate and respiratory variability allows to find out the very low frequency (VLF) rhythm. However it is not known, it is necessary to carry this rhythm to what type of wave processes. The purpose of the present researches was to study the respiratory variability and the variability of gas exchange parameters. 10 healthy subjects have been surveyed. The pneumogramms within 30 minutes spent record, and then a method "breath-by-breath" within 30 minutes registered gas exchange parameters (Ve--lung ventilation, V(O2) -O2 consumption and other parameters). Fast Fourier transform method has found out two groups of the basic peaks. The first--in a range 0.2-0.3 Hz (a time cycle--3-5 s), that corresponds respiratory frequency which size at subjects varied from 12 to 20 per minute. The second--in a range 0.002-0.0075 Hz, that corresponds VLF diapason (a time cycle--1-3.5 minutes). At the analysis pneumogramms rhythms in the same ranges have been established. The carried out researches allow to draw a conclusion on steady character of wave process in a VLF-range. It can be carried to quasi-periodic oscillations type. First oscillator or respiratory frequency it is formed by means of mechanisms of chemoreception. Considering, that V(O2) and V(CO2) are function energy exchange, it is possible to believe, what exactly energy demand define the second oscillator.     

Ventilatory responses to temperature variation in the fresh water turtle,Mauremys caspica leprosa

A study of lung gas exchange in the fresh water turtle Mauremys caspica leprosa at normal physiological body temperatures (15, 25 and 35 °C) was extended to extreme temperatures (5 and 40 °C) to determine whether the direct relationship between body temperature and ventilatory response found in many lung-breathing ectotherms including other chelonian species was maintained. From 5 to 35 °C the lung ventilation per unit of O₂ uptake and CO₂ removed declined with temperature. Consequently, lung CO₂ partial pressure increased with temperature. Its value was maintained within narrow limits at each thermal constant, suggesting a suitable control throughout the complete ventilatory cycle. At 40 °C the ventilatory response showed the opposite trend. The ratios of ventilation to lung gas exchange increased compared to their values at 35 °C. The impact of this increased breathing-lowering the estimated mean alveolar CO₂ partial pressure-was nevertheless less than expected due to an increase in calculated physiological dead space. This suggests that the relative hyperventilation in response to hyperthermia found in Mauremys caspica leprosa is related to evaporative heat loss.Abbreviations BTPS body temperature, ambient pressure, saturated with water vapour - CTM critical thermal maximum - F_N2 fractional concentration of nitrogen - PA _CO2or PL _CO2 alveolar or lung CO₂ pressure - PA_O2or PL_O2 alveolar or lung O₂ pressure - PI_O2 inspired O₂ pressure - R respiratory exchange ratio - STPD standard temperature, standard pressure, dry - T _a ambient temperature - T _b body temperature - VA alveolar ventilation - VA/VCO₂ relative alveolar ventilation (alveolar ventilation per unit of CO₂ removed) - VO₂ O₂ uptake - VCO₂ CO₂ output - V _D anatomical dead space volume - V _D physiological dead space volume - VE/VO₂ ventilatory equivalent for O₂ - VE pulmonary ventilation or expiratory minute volume - VE/VCO₂ ventilatory equivalent for CO₂ - V _T tidal volume     

Energy requirements of Adélie penguin (Pygoscelis adeliae) chicks

Summary The energy requirements of Adélie penguin (Pygoscelis adeliae) chicks were analysed with respect to body mass (W, 0.145–3.35 kg, n=36) and various forms of activity (lying, standing, minor activity, locomotion, walking on a treadmill). Direct respirometry was used to measure O₂ consumption ( ) and CO₂ production. Heart rate (HR, bpm) was recorded from the ECG obtained by both externally attached electrodes and implantable HR-transmitters. The parameters measured were not affected by hand-rearing of the chicks or by implanting transmitters. HR measured in the laboratory and in the field were comparable. Oxygen uptake ranged from in lying chicks to at maximal activity, RQ=0.76. Metabolic rate in small wild chicks (0.14–0.38 kg) was not affected by time of day, nor was their feeding frequency in the colony (Dec 20–21). Regressions of HR on were highly significant (p< 0.0001) in transmitter implanted chicks (n=4), and two relationships are proposed for the pooled data, one for minor activities ( ), and one for walking ( ). Oxygen consumption, mass of the chick (2–3 kg), and duration of walking (T, s) were related as , whereas mass-specific O₂ consumption was related to walking speed (S, m·s^-1) as .Abbreviations bpm beats per minute - D distance walked (m) - ECG electrocardiogram - HR heart rate (bpm) - ns number of steps - RQ respiratory quotient - S walking speed (m·s^-1) - T time walked (s) - W body mass (kg)