Ventilatory accommodation of oxygen demand and respiratory water loss in a large bird,the emu (Dromaius novaehollandiae), and a re-examination of ventilatory allometry for birds

Ventilation was studied in the emu, a large flightless bird of mass 40kg, within the range of ambient temperatures from-5 to 45°C. Data for the emu and 21 other species were used to calculate allometric relationships for resting ventilatory parameters in birds (breath frequency=13.5 mass^-0.314; tidal volume=20.7 mass^1.0). At low ambient temperatures the ventilatory system must accommodate the increased metabolic demand for oxygen. In the emu this was achieved by a combination of increased tidal volume and increased oxygen extraction. Data from emus sitting and standing at-5°C, when metabolism is 1.5x and 2.6x basal metabolic rate, respectively, indicate that at least in the emu an increase in oxygen extraction can be stimulated by low temperature independent of oxygen demand. At higher ambient temperatures ventilation was increased to facilitate respiratory water loss. The emu achieved this by increased respiratory frequency. At moderate heat loads (30–35°C) tidal volume fell. This is usually interpreted as a mechanism whereby respiratory water loss can be increased without increasing parabronchial ventilation. At 45°C tidal volume increased; however, past studies have shown that CO₂ washout is minimal under these conditions. The mechanism whereby this is possible is discussed.Abbreviations BMR basal metabolic rate - BTPS body temperature, ambient pressure, saturated - EO ₂ oxygen extraction - EWL evaporative water loss - f _R ventilation frequency - RH relative humidity - RHL respiratory heat loss - SEM standard error of the mean - SNK student-Newman-Keuls multiple range test - STPD standard temperature and pressure, dry - T _a ambient temperatures(s) - T _b body temperature(s) - T _ex expired air temperature(s) - T _rh chamber excurrent air temperature - V _J ventilation - VO₂ oxygen consumption - V _T tidal volume - V/Q air ventilation to blood perfusion ratio     

Respiratory evaporation in panting fowl: Partition between the respiratory and buccopharyngeal pumps

Summary Ventilation (V) and respiratory water loss were measured in domestic fowlGallus gallus subjected to raised environmental temperatures (33±2°C) and breathing air, 8% O₂ in N₂, 3% CO₂ in air or 5% CO₂ in air. Birds breathing air underwent an 18.6-fold increase in respiratory frequency and a 5-fold reduction in tidal volume and panting was accompanied by vigorous gular flutter. Hypoxic and hypercapnic birds breathed more slowly and deeply and gular flutter was strongly inhibited. The ratio was similar to that predicted on the basis of the measured ventilation assuming saturation of expired gas at measured gular mucosal temperature in hypoxic and hypercapnic birds but 54% greater than the predicted value in birds panting in air. It is concluded that the excess water loss during normal panting results from tidal airflow generated independently by the buccopharyngeal pump and that buccopharyngeal ventilation is equivalent to 54% of the respiratory ventilation.     

Ein Beitrag zum Zusammenhang zwischen Stimme und Atmung bei V?geln

Zusammenfassung Beim nordamerikanischen Abendkernbeißer (Hesperiphona vespertina, Körpergewicht um 60 g) wurde die Atmung bei einer Reihe von Schreckrufen aufgezeichnet. Die Rufe wurden beim Ausatmen ausgestoßen, der Luftstrom war in Pulsationen von 55–60/sec zerlegt. Bei den dazwischen liegenden Einatmungen waren Atemstrom und Atemvolumen im Vergleich zur Ruhe erhöht. Die Einatmungsdauer betrug nur 0,1–0,15 sec, was der Atmung im Flug sehr ähnlich ist.

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Summary In the North American Evening Grosbeak (Hesperiphona vespertina, body weight about 60 g) the respiration was recorded during distress calls. The calls were produced in the expired airstream in pulsations of 55–60/sec. The inspirations lying between the calls had increased tidal volume and airflow velocity relative to rest. The duration of inspiration was only 0,1–0,15 sec, which is very similar to that in flight.

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Issued as N.R.C. No. 10 302.     

Evaluation of methodological and biological influences on the collection and composition of exhaled breath condensate

Abstract

The purpose of this inter-species comparison (calves and pigs) was to identify methodological and biological influences on the collection and composition of exhaled breath condensate (EBC). A total of 352 EBC samples were collected, whilst variables of ventilation were registered in parallel. Partial pressure of carbon dioxide (pCO₂) and pH were analysed in non-degassed EBC samples. The concentration of total protein in EBC was measured colorimetrically. In both species, lung function was evaluated before and after EBC collection. Statistical analyses were performed to study the effect of EBC collection on lung function and to identify the influence of ventilatory variables on the collection and composition of EBC. Collection of EBC did not affect lung function. Despite the volume of EBC collected per unit time being primarily dependent on ventilation per unit time, species-specific conditions during the EBC collection process resulted in different dependences of EBC collection from other variables of ventilation (i.e. maximal airflow during expiration or expired tidal volume kg^?1 body weight). The concentration of protein ml^?1 EBC increased with the expired volume per min and with peak expiratory flow. Although the pCO₂ in fresh EBC was significantly negatively dependent on the duration of collection, comparable pHs (5.6???6.2) were measured in EBC of both calves and pigs. The obtained data may help one standardize EBC collection in different species.     

Ventilatory response of the diamondback water snake,Natrix rhombifera to hypoxia, hypercapnia and increased oxygen demand

Summary Simultaneous measurements of ventilatory frequency, tidal volume, O₂ uptake, CO₂ output and cardiac frequency were made in the diamondback water snake,Natrix rhombifera while breathing hypoxic (15% to 5% O₂ in N₂) or hypercarbic (2% to 10% CO₂ and 21% O₂ in N₂) gases. The snakes responded to hypoxia by increasing tidal volume and decreasing ventilatory frequency resulting in little change in ventilation (50% increase at 5% inspired O₂), or O₂ uptake and only a light increase in CO₂ output. Hypercarbia to 4.2% inspired CO₂ resulted in a slight hyperventilation but ventilation was depressed at 6.3% inspired CO₂ and became erratic at higher concentrations. The resting rate of O₂ uptake was maintained throughout hypercapnia. Heart rate increased during hypoxia and decreased during hypercapnia. Cutaneous O₂ uptake increased during extreme hypoxia (5% inspired O₂) and cutaneous CO₂ output increased during hypercapnia, probably due to changes in the body-to-ambient gas gradients (Crawford and Schultetus, 1970). Both pulmonary oxygen uptake and ventilation were dramatically increased immediately following 10–15 min experimental dives. The increased ventilation was achieved primarily through an increased tidal volume.     

Exhaled air temperature as a function of ambient temperature in flying and resting ducks

Exhaled air temperature (T _exh) has a paramount effect on respiratory water loss during flight. For migratory birds, low T _exh potentially reduces water loss and increases flight range. However, only three studies provide empirical data on T _exh during flight. The aim of this study was to record T _exh of birds during rest and flight at a range of controlled ambient temperatures (T _amb). One wigeon and two teal flew a total of 20 times in a wind tunnel at T _amb ranging from 1° to 24°C. T _exh during flight did not differ between the two species and was strongly correlated with T _amb (T _exh=1.036 T _amb + 13.426; R²=0.58). In addition, body temperature had a weak positive effect on T _exh. At a given T _amb, T _exh was about 5°C higher during flight than at rest.     

A system to simulate gas exchange in humans to control quality of metabolic measurements

We have developed a gas exchange simulation system (GESS) to assess the quality control in measurements of metabolic gas exchange. The GESS simulates human breathing from rest to maximal exercise. It approximates breath-by-breath waveforms, ventilatory output, gas concentrations, temperature and humidity during inspiration and expiration. A programmable motion control driving two syringes allows the ventilation to be set at any tidal volume (V _T), respiratory frequency (f), flow waveform and period of inspiration and expiration. The GESS was tested at various combinations of V _T (0.5–2.5 l) and f (10–60 stroke · min⁻¹) and at various fractional concentrations of expired oxygen (0.1294–0.1795); and carbon dioxide (0.0210–0.0690) for a pre-set flow waveform and for expired gases at the same temperature and humidity as room air. Expired gases were collected in a polyethylene bag for measurement of volume and gas concentrations. Accuracy was assessed by calculating the absolute and relative errors on parameters (error = measured−predicted). The overall error in the gas exchange values averaged less than 2% for oxygen uptake and carbon dioxide output, which is within the accuracy of the Douglas bag method. Accepted: 4 June 1998     

Metabolic responses of homing pigeons to flight and subsequent recovery

This study examines metabolic changes occurring during short to endurance flights and during subsequent recovery in free-flying pigeons, in particular the change towards lipid utilization with increasing flight duration, lipid supply to the flight muscles, protein utilization and the time needed to metabolically recover. Eight plasma metabolite concentrations were measured in homing pigeons released from sites 20–200 km from the loft (0.3–4.8 h flight duration) just after landing and after keeping birds fasting at rest for 30 and 60 min, respectively, after their return. Birds kept in the loft fasting at rest were used as controls. Plasma free fatty acid and glycerol concentrations increased rapidly with flight duration and leveled off after about 1.5 h. This indicates a marked change towards a high and stable lipid utilization from adipose tissues within 1–2 h of flight. Plasma triglyceride levels and very-low-density lipoproteins were decreased after short flights, but subsequently regained or surpassed fasting levels at rest. This indicates that re-esterification of free fatty acids and delivery as very-low-density lipoproteins to the flight muscles to circumvent constraints of fatty acid supply, as described previously for small passerines, is not as significant in the pigeon which has a much lower mass-specific energy rate. An initial increase in plasma glucose levels and a transient decrease to fasting levels at rest was observed and may reflect the initial use and subsequent exhaustion of glycogen stores. Contrary to other birds and mammals, -hydroxy-butyrate levels increased markedly with flight duration. This may suggest a more important sparing of carbohydrates and protein as gluconeogenic precursors in the pigeon than in other species. Plasma uric acid levels increased linearly up to about 4 h flight duration. This indicates an accelerated protein breakdown during flight which may primarily serve to deliver amino acids as glucogenic precursors and citrate cycle intermediates. With increasing flight duration, the energy sources change from an initial phase based primarily on carbohydrates to a lipid-based endurance phase. It is discussed whether this metabolic change depends on the level of power output or the performed work (energy spent) since the start of flight. During the first hour of recovery, most metabolites reached or approached fasting levels at rest, indicating a marked reduction in lipolysis and protein breakdown. -hydroxy-butyrate levels remained at flight levels and glucose levels increased slightly, indicating a restoration of glycogen stores.Abbreviations VLDL very-low-density lipoproteins - FFA free fatty acids     

Flight modes in migrating European bee-eaters: heart rate may indicate low metabolic rate during soaring and gliding

Background

Many avian species soar and glide over land. Evidence from large birds (m _b>0.9 kg) suggests that soaring-gliding is considerably cheaper in terms of energy than flapping flight, and costs about two to three times the basal metabolic rate (BMR). Yet, soaring-gliding is considered unfavorable for small birds because migration speed in small birds during soaring-gliding is believed to be lower than that of flapping flight. Nevertheless, several small bird species routinely soar and glide.

Methodology/Principal Findings

To estimate the energetic cost of soaring-gliding flight in small birds, we measured heart beat frequencies of free-ranging migrating European bee-eaters (Merops apiaster, m _b∼55 g) using radio telemetry, and established the relationship between heart beat frequency and metabolic rate (by indirect calorimetry) in the laboratory. Heart beat frequency during sustained soaring-gliding was 2.2 to 2.5 times lower than during flapping flight, but similar to, and not significantly different from, that measured in resting birds. We estimated that soaring-gliding metabolic rate of European bee-eaters is about twice their basal metabolic rate (BMR), which is similar to the value estimated in the black-browed albatross Thalassarche (previously Diomedea) melanophrys, m _b∼4 kg). We found that soaring-gliding migration speed is not significantly different from flapping migration speed.

Conclusions/Significance

We found no evidence that soaring-gliding speed is slower than flapping flight in bee-eaters, contradicting earlier estimates that implied a migration speed penalty for using soaring-gliding rather than flapping flight. Moreover, we suggest that small birds soar and glide during migration, breeding, dispersal, and other stages in their annual cycle because it may entail a low energy cost of transport. We propose that the energy cost of soaring-gliding may be proportional to BMR regardless of bird size, as theoretically deduced by earlier studies.     

Noninvasive Measurement of Carbon Dioxide during One-Lung Ventilation with Low Tidal Volume for Two Hours: End-Tidal versus Transcutaneous Techniques

BackgroundThere may be significant difference between measurement of end-tidal carbon dioxide partial pressure (PetCO₂) and arterial carbon dioxide partial pressure (PaCO₂) during one-lung ventilation with low tidal volume for thoracic surgeries. Transcutaneous carbon dioxide partial pressure (PtcCO₂) monitoring can be used continuously to evaluate PaCO₂ in a noninvasive fashion. In this study, we compared the accuracy between PetCO₂ and PtcCO₂ in predicting PaCO₂ during prolonged one-lung ventilation with low tidal volume for thoracic surgeries.MethodsEighteen adult patients who underwent thoracic surgeries with one-lung ventilation longer than two hours were included in this study. Their PetCO₂, PtcCO₂, and PaCO₂ values were collected at five time points before and during one-lung ventilation. Agreement among measures was evaluated by Bland-Altman analysis.ResultsNinety sample sets were obtained. The bias and precision when PtcCO₂ and PaCO₂ were compared were 4.1 ± 6.5 mmHg during two-lung ventilation and 2.9 ± 6.1 mmHg during one-lung ventilation. Those when PetCO₂ and PaCO₂ were compared were -11.8 ± 6.4 mmHg during two-lung ventilation and -11.8 ± 4.9 mmHg during one-lung ventilation. The differences between PtcCO₂ and PaCO₂ were significantly lower than those between PetCO₂ and PaCO₂ at all five time-points (p < 0.05).ConclusionsPtcCO₂ monitoring was more accurate for predicting PaCO₂ levels during prolonged one-lung ventilation with low tidal volume for patients undergoing thoracic surgeries.     

Ventilatory physiology of the numbat (<Emphasis Type="Italic">Myrmecobius fasciatus</Emphasis>)

This study examines the ventilatory physiology of the numbat (Myrmecobius fasciatus), a small to medium-sized (550 g) termitivorous marsupial. Ventilatory parameters at thermoneutrality reflect the slightly low (83% of predicted) basal metabolic rate of the numbat, with ventilation frequency (ƒ_R; 30.6±3.65 breaths min^–1), tidal volume [V_T; 6.0±0.66 ml at body temperature and pressure, saturated (BTPS)] and consequently minute volume (V_I; 117.7±15.22 ml min^–1; BTPS) all being 80–87% of that expected for a marsupial of similar body mass. Oxygen extraction was 27.7±1.37% in the thermoneutral zone. As is typical of marsupials, numbats accommodated increased oxygen consumption rates at ambient temperatures (T _a) below the thermoneutral zone by increasing minute volume (up to 411.2±43.98 ml min^–1; BTPS at T _a=10 °C) rather than oxygen extraction. Minute volume at 10 °C increased more by changes in ventilation frequency (up to 45.5±4.85 breaths min^–1) than tidal volume (9.4±1.03 ml, BTPS), as is also typical for a small-medium sized marsupial.Abbreviations BMR basal metabolic rate - BTPS body temperature and pressure, saturated - EO ₂ oxygen extraction - ƒ _R ventilation frequency - STPD standard temperature and pressure, dry - T _a ambient temperature - T _b body temperature - TNZ thermoneutral zone - V _I minute volume - V _T tidal volume - O ₂ oxygen consumption rate Communicated by I.D. Hume     

Respiratory,cardiovascular and metabolic adjustments during steady state swimming in the green turtle,Chelonia mydas

Summary Heart rate and pulmonary artery blood flow of resting green turtles,Chelonia mydas, at 29°C increased with lung ventilation (heart rate from 24±5 to 51±8 beats min). When swimming at 0.6 m s^–1 in water at 30°C, oxygen uptake was 2.83 times and respiratory frequency was 2.75 times the resting values. Heart rate was 1.33 times that during ventilation at rest but 2.83 times that at the end of a breath hold at rest. Partial pressures of oxygen and carbon dioxide, lactic acid concentration and pH of arterial blood, when swimming at 0.5 m s^–1, were similar to those soon after ventilation at rest. Pulmonary blood flow did not decline to low levels between breaths, when the animals were swimming, as it did when they were at rest.In active turtles it appears that pulmonary perfusion remains elevated, supplying oxygen to the locomotory muscles at a sufficiently high rate to support the complete aerobic production of energy, and that respiratory frequency is kept as low as possible, as surfacing for air increases the metabolic cost of swimming.     

Lung Protective Ventilation Induces Immunotolerance and Nitric Oxide Metabolites in Porcine Experimental Postoperative Sepsis

Low tidal volume ventilation is beneficial in patients with severe pulmonary dysfunction and would, in theory, reduce postoperative complications if implemented during routine surgery. The study aimed to investigate whether low tidal volume ventilation and high positive end-expiratory pressure (PEEP) in a large animal model of postoperative sepsis would attenuate the systemic inflammatory response and organ dysfunction. Thirty healthy pigs were randomized to three groups: Group Prot-7h, i.e. protective ventilation for 7 h, was ventilated with a tidal volume of 6 mL x kg^-1 for 7 h; group Prot-5h, i.e. protective ventilation for 5 h, was ventilated with a tidal volume of 10 mL x kg^-1 for 2 h, after which the group was ventilated with a tidal volume of 6 mL x kg^-1; and a control group that was ventilated with a tidal volume of 10 mL x kg^-1 for 7 h. In groups Prot-7h and Prot-5h PEEP was 5 cmH₂O for 2 h and 10 cmH₂O for 5 h. In the control group PEEP was 5 cmH₂O for the entire experiment. After surgery for 2 h, postoperative sepsis was simulated with an endotoxin infusion for 5 h. Low tidal volume ventilation combined with higher PEEP led to lower levels of interleukin 6 and 10 in plasma, higher PaO₂/FiO2, better preserved functional residual capacity and lower plasma troponin I as compared with animals ventilated with a medium high tidal volume and lower PEEP. The beneficial effects of protective ventilation were seen despite greater reductions in cardiac index and oxygen delivery index. In the immediate postoperative phase low V_T ventilation with higher PEEP was associated with reduced ex vivo plasma capacity to produce TNF-α upon endotoxin stimulation and higher nitrite levels in urine. These findings might represent mechanistic explanations for the attenuation of systemic inflammation and inflammatory-induced organ dysfunction.     

Ventilation of an additional dead space

The authors studied the question of the completeness of ventilation of an additional dead space in the form of a tube 3 cm in diameter and with a volume of 600 ml. Seven young volunteers were examined while breathing with and without the tube, seated at rest and during a two-grade exercise load on a bicycle ergometer. The criterion of ventilation of the tube was enlargement of the dead space by 600 ml during breathing through the tube. The functional dead space was always calculated from the tidal volume and the CO2 concentration in mixed expired air and in an end-tidal sample, using the Bohr equation. In every case, the tube was found to be completely ventilated by breathing, both under resting conditions and during exercise. In breathing during the bicycle exercise, the ratio of the functional dead space to tidal volume fell from 0.3 to 0.19 and a similar decrease was recorded in breathing through the tube.     

End-tidal CO2 in some aquatic mammals of large size

While resting on land or at the water surface, the breathing frequency (f) of aquatic mammals of medium and large size is lower than in terrestrial mammals of similar body weight (W), the difference widening with the increase in W. The allometric function for aquatic mammals is f∝W^?0.42 (f, breaths/min, W, kg) and that of terrestrial species is f∝W^?0.25. We asked whether or not resting breathing at such low f would entail high values of alveolar CO₂. End-tidal alveolar CO₂ pressure, taken as representative of alveolar CO₂ pressure, PaCO₂, was measured from the expired gas during resting breathing in captive specimens of aquatic species trained to rest in proximity of their keepers, either on land (walrus and sea lion) or at the water surface (dolphin, orca, beluga and hippopotamus). Their f during the recordings ranged from less than 1 (orca) to 6 (walrus) breaths/min. The average PaCO₂ values ranged from 32 to 42 mm Hg, the peaks being a few mm Hg higher. These values were similar or slightly higher than literature data of many terrestrial species, with no relation to the animal f or W. The quasi-normality of PaCO₂ in large aquatic species breathing at rest, despite their exceptionally low f and normal metabolism, can be explained mainly by two factors, their large tidal volume/W, about three times the average terrestrial value, and their peculiar breathing pattern with sustained high lung volume during the expiratory pause. This latter is key in avoiding a substantial rise in PaCO₂ during the inter-breath pause.     

Stopover and fat deposition by North American wood-warblers (Parulinae) following spring migration over the Gulf of Mexico

Summary Length of stopover and rate of weight gain (fat deposition) were studied in several species of passerine birds that stopped in southwestern Louisiana along the northern coast of the Gulf of Mexico after a trans-Gulf flight. Fatdepleted birds were more common among the birds that arrived at our study site in southwest Louisiana, though variability characterized our samples. Migrants that landed after encountering opposing winds or rain over the northern Gulf of Mexico were, on average, fatter than migrants that landed when weather was favorable for continued migration. Some of the variation in the energetic condition of arrivals may be explained by the location where migrants initiated crossings. Our simulation of flight over the Gulf of Mexico showed that with following winds a warbler can cross the Gulf of Mexico from Yucatan with fat reserves to spare, and stronger tailwinds make flights from as far south as Honduras energetically permissible. The length of stay after a trans-Gulf flight was related to the extent of fat-depletion upon arrival: lean birds stayed longer than fat migrants. Migrants stopped over for 1–7 days and replenished energy reserves at rates that varied from 0.19 g/d for Hooded Warblers (Wilsonia citrina) to 0.87 g/d for Ovenbirds (Seiurus aurocapillus). Within each species, most individuals gained weight at a rapid rate, though a few individuals lost or maintained weight during their stay.     

Effect of PEEP and Tidal Volume on Ventilation Distribution and End-Expiratory Lung Volume: A Prospective Experimental Animal and Pilot Clinical Study

Introduction

Lung-protective ventilation aims at using low tidal volumes (V_T) at optimum positive end-expiratory pressures (PEEP). Optimum PEEP should recruit atelectatic lung regions and avoid tidal recruitment and end-inspiratory overinflation. We examined the effect of V_T and PEEP on ventilation distribution, regional respiratory system compliance (C_RS), and end-expiratory lung volume (EELV) in an animal model of acute lung injury (ALI) and patients with ARDS by using electrical impedance tomography (EIT) with the aim to assess tidal recruitment and overinflation.

Methods

EIT examinations were performed in 10 anaesthetized pigs with normal lungs ventilated at 5 and 10 ml/kg body weight V_T and 5 cmH₂O PEEP. After ALI induction, 10 ml/kg V_T and 10 cmH₂O PEEP were applied. Afterwards, PEEP was set according to the pressure-volume curve. Animals were randomized to either low or high V_T ventilation changed after 30 minutes in a crossover design. Ventilation distribution, regional C_RS and changes in EELV were analyzed. The same measures were determined in five ARDS patients examined during low and high V_T ventilation (6 and 10 (8) ml/kg) at three PEEP levels.

Results

In healthy animals, high compared to low V_T increased C_RS and ventilation in dependent lung regions implying tidal recruitment. ALI reduced C_RS and EELV in all regions without changing ventilation distribution. Pressure-volume curve-derived PEEP of 21±4 cmH₂O (mean±SD) resulted in comparable increase in C_RS in dependent and decrease in non-dependent regions at both V_T. This implied that tidal recruitment was avoided but end-inspiratory overinflation was present irrespective of V_T. In patients, regional C_RS differences between low and high V_T revealed high degree of tidal recruitment and low overinflation at 3±1 cmH₂O PEEP. Tidal recruitment decreased at 10±1 cmH₂O and was further reduced at 15±2 cmH₂O PEEP.

Conclusions

Tidal recruitment and end-inspiratory overinflation can be assessed by EIT-based analysis of regional C_RS.     

Evaluation of methodological and biological influences on the collection and composition of exhaled breath condensate

The purpose of this inter-species comparison (calves and pigs) was to identify methodological and biological influences on the collection and composition of exhaled breath condensate (EBC). A total of 352 EBC samples were collected, whilst variables of ventilation were registered in parallel. Partial pressure of carbon dioxide (pCO₂) and pH were analysed in non-degassed EBC samples. The concentration of total protein in EBC was measured colorimetrically. In both species, lung function was evaluated before and after EBC collection. Statistical analyses were performed to study the effect of EBC collection on lung function and to identify the influence of ventilatory variables on the collection and composition of EBC. Collection of EBC did not affect lung function. Despite the volume of EBC collected per unit time being primarily dependent on ventilation per unit time, species-specific conditions during the EBC collection process resulted in different dependences of EBC collection from other variables of ventilation (i.e. maximal airflow during expiration or expired tidal volume kg^-1 body weight). The concentration of protein ml^-1 EBC increased with the expired volume per min and with peak expiratory flow. Although the pCO₂ in fresh EBC was significantly negatively dependent on the duration of collection, comparable pHs (5.6 - 6.2) were measured in EBC of both calves and pigs. The obtained data may help one standardize EBC collection in different species.     

Cross sectional geometry of the forelimb skeleton and flight mode in pelecaniform birds

Avian wing elements have been shown to experience both dorsoventral bending and torsional loads during flapping flight. However, not all birds use continuous flapping as a primary flight strategy. The pelecaniforms exhibit extraordinary diversity in flight mode, utilizing flapping, flap‐gliding, and soaring. Here we (1) characterize the cross‐sectional geometry of the three main wing bone (humerus, ulna, carpometacarpus), (2) use elements of beam theory to estimate resistance to loading, and (3) examine patterns of variation in hypothesized loading resistance relative to flight and diving mode in 16 species of pelecaniform birds. Patterns emerge that are common to all species, as well as some characteristics that are flight‐ and diving‐mode specific. In all birds examined, the distal most wing segment (carpometacarpus) is the most elliptical (relatively high I_max/I_min) at mid‐shaft, suggesting a shape optimized to resist bending loads in a dorsoventral direction. As primary flight feathers attach at an oblique angle relative to the long axis of the carpometacarpus, they are likely responsible for inducing bending of this element during flight. Moreover, among flight modes examined the flapping group (cormorants) exhibits more elliptical humeri and carpometacarpi than other flight modes, perhaps pertaining to the higher frequency of bending loads in these elements. The soaring birds (pelicans and gannets) exhibit wing elements with near‐circular cross‐sections and higher polar moments of area than in the flap and flap‐gliding birds, suggesting shapes optimized to offer increased resistance to torsional loads. This analysis of cross‐sectional geometry has enhanced our interpretation of how the wing elements are being loaded and ultimately how they are being used during normal activities. J. Morphol., 2011. © 2011 Wiley‐Liss,Inc.     

Ventilatory accommodation of changing oxygen demand in sciurid rodents

Summary Ventilation was measured across a range of O₂ consumption rates in four sciurid rodents: Tamias minimus (47 g), Spermophilus lateralis (189 g), S. beecheyi (531 g), and Marmota flaviventris juveniles (1054 g) and adults (2989 g). Maximum thermogenic oxygen consumption was measured for all but adult M. flaviventris. Aerobic scopes (maximum/minimum O₂ consumption rates) were 4.6, 3.8, 5.4, and 4.8 in T. minimus, S. lateralis, S. beecheyi, and juvenile M. flaviventris, respectively. Aerobic scope was at least 4.1 in adult M. flaviventris. Ventilatory accommodation of changing O₂ consumption rate was qualitatively similar in the four species, with the bulk of accommodation resulting from changes in minute volume. Nevertheless, there were significant differences in the relative importance of frequency, tidal volume, and O₂ extraction in accommodation. In all species, frequency and minute volume were strongly correlated to O₂ consumption rate. Tidal volume was significantly correlated to O₂ consumption rate in T. minimus and S. beecheyi, but not in the other species. Oxygen extraction was not significantly correlated to O₂ consumption rate in any species. Analysis of factorial ventilation changes across a standardized 3.8-fold change in O₂ consumption rate revealed significant differences among species in frequency and O₂ extraction, but not in tidal or minute volume. When compared to a generalized allometry for mammalian resting ventilation, the four sciurid species had consistently lower respiration frequency and higher O₂ extraction than predicted, perhaps because the sciurid measurements were made on unrestrained animals. There was no indication that ventilation constrained maximum O₂ consumption rate.Abbreviations BMR basal metabolic rate - BTPS body temperature and pressure saturated - EO₂ oxygen extraction - f respiration frequency - MMR minimal metabolic rate - RH relative humidity - STPD standard pressure and temperature, dry - T _a ambient temperature - T _b body temperature - minute volume - tidal volume - maximum rate of oxygen consumption