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Ponganis, PJ, Stockard TK.  2007.  The Antarctic toothfish: how common a prey for Weddell seals? Antarctic Science. 19:441-442.   10.1017/s0954102007000715   AbstractWebsite

The Antarctic toothfish (Dissostichus mawsoni Norman) has been considered an occasional large prey item of the Weddell seal (Leptonychotes weddellii Lesson) (Kooyman 1967, Calhaem & Christoffel 1969, Testa et al. 1985, Castellini et al. 1992, Davis et al. 1999, Fuiman et al. 2002). The seal's most common prey is the Antarctic silverfish (Pleuragramma antarcticum Boulenger) as well as benthic and sub-ice fish, cephalopods, and crustaceans (Dearborn 1965, Green & Burton 1987, Plotz 1987, Plotz et al. 1991, Castellini et al. 1992, Burns et al. 1998).

Ponganis, PJ, Ponganis EP, Ponganis KV, Kooyman GL, Gentry RL, Trillmich F.  1990.  Swimming velocities in otariids. Canadian Journal of Zoology-Revue Canadienne De Zoologie. 68:2105-2112.   10.1139/z90-293   AbstractWebsite

Velocities during surface swimming and diving were measured with microprocessor recorders in four otariid species: northern fur seals (Callorhinusursinus), Galapagos sea lions (Zalophuscalifornianuswollebaeki), Galapagos fur seals (Arctocephalusgalapagoensis), and Hooker's sea lions (Phocarctoshookeri). Mean surface swimming velocities ranged from 0.6 to 1.9 m/s. Transit distances to feeding sites (1.2–90 km) were calculated using these velocities. Dive velocities, recorded every 15 s, ranged from 0.9 to 1.9 m/s. These velocities were consistent with calculated minimal cost of transport velocities in the smaller species. Using time partitioning, the metabolic cost of a northern fur seal foraging trip is estimated on the basis of recorded velocities and their calculated energy costs. This value is within 6% of that previously made with doubly labeled water techniques.

Ponganis, PJ, Kooyman GL, Sartoris D, Jobsis P.  1992.  Pinniped splenic volumes. American Journal of Physiology. 262:R322-R325. AbstractWebsite

Splenic volume was measured by computerized axial tomography in three harbor seals (Phoca vitulina) and two California sea lions (Zalophus californianus). Volumes ranged from 228 to 679 ml, representing 0.8-3.0% of calculated percentage body mass. Despite possible variation in the state of splenic contraction during the examination, these values are in the upper range of reported mammalian splenic volumes (as % of body mass). This reinforces the pinniped splenic erythrocyte storage concept.

Ponganis, PJ, Van Dam RP, Levenson DH, Knower T, Ponganis KV, Marshall G.  2003.  Regional heterothermy and conservation of core temperature in emperor penguins diving under sea ice. Comparative Biochemistry and Physiology a-Molecular & Integrative Physiology. 135:477-487.   10.1016/s1095-6433(03)00133-8   AbstractWebsite

Temperatures were recorded at several body sites in emperor penguins (Aptenodytes forsteri) diving at an isolated dive hole in order to document temperature profiles during diving and to evaluate the role of hypothermia in this well-studied model of penguin diving physiology. Grand mean temperatures (+/-S.E.) in central body sites during dives were: stomach: 37.1 +/- 0.2 degreesC (n = 101 dives in five birds), pectoral muscle: 37.8 +/- 0.1 degreesC (n = 71 dives in three birds) and axillary/brachial veins: 37.9 +/- 0.1 degreesC (n = 97 dives in three birds). Mean diving temperature and duration correlated negatively at only one site in one bird (femoral vein, r = -0.59, P < 0.05; range < 1 degreesC). In contrast, grand mean temperatures in the wing vein, foot vein and lumbar subcutaneous tissue during dives were 7.6 +/- 0.7 degreesC (n = 157 dives in three birds), 20.2 +/- 1.2 degreesC (n = 69 in three birds) and 35.2 +/- 0.2 degreesC (n = 261 in six birds), respectively. Mean limb temperature during dives negatively correlated with diving duration in all six birds (r = -0.29 to -0.60, P < 0.05). In two of six birds, mean diving subcutaneous temperature negatively correlated with diving duration (r = -0.49 and -0.78, P < 0.05). Sub-feather temperatures decreased from 31 to 35 T during rest periods to a grand mean of 15.0 +/- 0.7 degreesC during 68 dives of three birds; mean diving temperature and duration correlated negatively in one bird (r = -0.42, P < 0.05). In general, pectoral, deep venous and even stomach temperatures during diving reflected previously measured vena caval temperatures of 37-39 degreesC more closely than the anterior abdominal temperatures (19-30 degreesC) recently recorded in diving emperors. Although prey ingestion can result in cooling in the stomach, these findings and the lack of negative correlations between internal temperatures and diving duration do not support a role for hypothermia-induced metabolic suppression of the abdominal organs as a mechanism of extension of aerobic dive time in emperor penguins diving at the isolated dive hole. Such high temperatures within the body and the observed decreases in limb, anterior abdomen, subcutaneous and sub-feather temperatures are consistent with preservation of core temperature and cooling of an outer body shell secondary to peripheral vasoconstriction, decreased insulation of the feather layer, and conductive/convective heat loss to the water environment during the diving of these emperor penguins. (C) 2003 Elsevier Science Inc. All fights reserved.

Ponganis, PJ, Meir JU, Williams CL.  2010.  Oxygen store depletion and the aerobic dive limit in emperor penguins. Aquatic Biology. 8:237-245.   10.3354/ab00216   AbstractWebsite

The aerobic dive limit (ADL), dive duration associated with the onset of post-dive blood lactate elevation, has been widely used in the interpretation of diving physiology and diving behavior. However, its physiological basis is incompletely understood, and in most studies, ADLs are simply calculated with an O(2) store/O(2) consumption formula. To better understand the ADL, research has been conducted on emperor penguins diving at an isolated dive hole. This work has revealed that O(2) stores are greater than previously estimated, and that the rate of depletion of those O(2) stores appears to be regulated primarily through a diving bradycardia and the efficiency of swimming. Blood and respiratory O(2) stores are not depleted at the 5.6 min ADL determined by post-dive blood lactate measurements. It is hypothesized that muscle, isolated from the circulation during a dive, is the primary source of lactate accumulation. To predict this 5.6 min ADL for these shallow dives at the isolated dive hole with the classic O(2) store/O(2) consumption formula, an O(2) consumption rate of 2x the predicted metabolic rate of a penguin at rest is required. In contrast, if the formula is used to calculate an ADL that is defined as the time for all consumable O(2) stores to be depleted, then a 23.1 min dive, in which final venous partial pressure of oxygen (P(O2)) was 6 mm Hg (0.8 kPa), represents such a maximum limit and demonstrates that an O(2) consumption rate of about 0.5x the predicted rate of an emperor penguin at rest is required in the formula.

Ponganis, PJ, Kooyman GL, Baranov EA, Thorson PH, Stewart BS.  1997.  The aerobic submersion limit of Baikal seals, Phoca sibirica. Canadian Journal of Zoology-Revue Canadienne De Zoologie. 75:1323-1327.   10.1139/z97-756   AbstractWebsite

An aerobic dive limit (ADL), the diving duration beyond which postdive lactate concentration increases above the resting level, has been estimated theoretically for many species. Such calculations have been based on an oxygen store/diving metabolic rate (MR) equation. Until now, an ADL has been determined empirically from measurements of blood lactate concentration only in the Weddell seal, Leptonychotes weddellii. We measured post-submergence plasma lactate concentrations during spontaneous voluntary submersions of three captive adult Baikal seals (Phoca sibirica). Two-phase regression analysis revealed a transition in the lactate concentration - submersion duration relationship after the animal had been diving for 15 min. Data collected in prior studies on oxygen stores and submersion metabolic rates of Baikal seals yielded a calculated aerobic limit of 16 min. As in Weddell seals, the empirically determined aerobic limit was very similar to the theoretical limit. Furthermore, most diving durations recorded during recent studies of free-ranging Baikal seals are under this limit. These data support the concept of an ADL and its estimation by means of an oxygen store/diving MR calculation.

Ponganis, PJ, Stockard TK, Levenson DH, Berg L, Baranov EA.  2006.  Cardiac output and muscle blood flow during rest-associated apneas of elephant seals. Comparative Biochemistry and Physiology a-Molecular & Integrative Physiology. 144:105-111.   10.1016/j.cbpa.2006.02.009   AbstractWebsite

In order to evaluate hemodynamics and blood flow during rest-associated apnea in young elephant seals (Mirounga angustirostris), cardiac outputs (CO, thermodilution), heart rates (HR), and muscle blood flow (MBF, laser Doppler flowmetry) were measured.. Mean apneic COs and HRs of three seals were 46% and 39% less than eupneic values, respectively (2.1 +/- 0.3 vs. 4.0 +/- 0.1 mL kg(-1) s(-1), and 54 6 vs. 89 14 beats min(-1)). The mean apneic stroke volume (SV) was not significantly different from the eupneic value (2.3 +/- 0.2 vs. 2.7 +/- 0.5 mL kg(-1)). Mean apneic MBF of three seals was 51% of the eupneic value. The decline in MBF during apnea was gradual, and variable in both rate and magnitude. In contrast to values previously documented in seals during forced submersions (FS), CO and SV during rest-associated apneas were maintained at levels characteristic of previously published values in similarly-sized terrestrial mammals at rest. Apneic COs of such magnitude and incomplete muscle ischemia during the apnea suggest that (1) most organs are not ischemic during rest-associated apneas, (2) the blood O-2 depletion rate is greater during rest-associated apneas than during FS, and (3) the blood O-2 store is not completely isolated from muscle during rest-associated apneas. (c) 2006 Elsevier Inc. All rights reserved.

Ponganis, PJ, Kreutzer U, Sailasuta N, Knower T, Hurd R, Jue T.  2002.  Detection of myoglobin desaturation in Mirounga angustirostris during apnea. American Journal of Physiology-Regulatory Integrative and Comparative Physiology. 282:R267-R272. AbstractWebsite

H-1 NMR solution-state study of elephant seal (Mirounga angustirostris) myoglobin (Mb) and hemoglobin (Hb) establishes the temperature-dependent chemical shifts of the proximal histidyl NdeltaH signal, which reflects the respective intracellular and vascular PO2 in vivo. Both proteins exist predominantly in one major isoform and do not exhibit any conformational heterogeneity. The Mb and Hb signals are detectable in M. angustirostris tissue in vivo. During eupnea M. angustirostris muscle maintains a well-saturated MbO(2). However, during apnea, the deoxymyoglobin proximal histidyl NdeltaH signal becomes visible, reflecting a declining tissue PO2. The study establishes a firm methodological basis for using NMR to investigate the metabolic responses during sleep apnea of the elephant seal and to secure insights into oxygen regulation in diving mammals.

Ponganis, PJ, McDonald BI, Tift MS, Gonzalez SC, DaValle B, Gliniecki RA, Stehman CC, Hauff N, Ruddick B, Howard R.  2017.  Effects of inhalational anesthesia on blood gases and pH in California sea lions. Marine Mammal Science. 33:726-737.   10.1111/mms.12388   AbstractWebsite

Despite the widespread use of inhalational anesthesia with spontaneous ventilation in many studies of otariid pinnipeds, the effects and risks of anesthetic-induced respiratory depression on blood gas and pH regulation are unknown in these animals. During such anesthesia in California sea lions (Zalophus californianus), blood gas and pH analyses of opportunistic blood samples revealed routine hypercarbia (highest P-CO2 = 128 mm Hg [17.1 kPa]), but adequate arterial oxygenation (P-O2 > 100 mm Hg [13.3 kPa] on 100% inspiratory oxygen). Respiratory acidosis (lowest pH = 7.05) was limited by the increased buffering capacity of sea lion blood. Amarkedly widened alveolar-to-arterial P-O2 difference was indicative of atelectasis and ventilation-perfusion mismatch in the lung secondary to hypoventilation during anesthesia. Despite the generally safe track record of this anesthetic regimen in the past, these findings demonstrate the value of high inspiratory O-2 concentrations and the necessity of constant vigilance and caution. In order to avoid hypoxemia, we emphasize the importance of late extubation or at least maintenance of mask ventilation on O-2 until anesthetic-induced respiratory depression is resolved. In this regard, whether for planned or emergency application, we also describe a simple, easily employed intubation technique with the Casper zalophoscope for sea lions.

Ponganis, PJ, Kooyman GL.  1999.  Heart rate and electrocardiogram characteristics of a young California gray whale (Eschrichtius robustus). Marine Mammal Science. 15:1198-1207.   10.1111/j.1748-7692.1999.tb00885.x   AbstractWebsite

Electrocardiogram (ECG) analyses of Holter monitor recordings from a young California gray whale were performed to determine ECG waveform characteristics, evaluate the heart rate pattern for sinus arrhythmia, obtain resting heart rates at known body masses as the whale increased in size, and compare those heart rates with predicted heart rates from allometric equations. The PR and QRS intervals (475 +/- 35 msec, 208 +/- 24 msec, respectively, n = 20) support the concept (Meijler et al. 1992) that atrioventricular transmission and ventricular excitation times do not increase linearly in very large mammals. A sinus arrhythmia pattern at rest (apneic heart rates of 15-25 beats per min [bpm] and eupneic heart rates of 34-40 bpm) is consistent with a relative eupneic tachycardia and apneic bradycardia during diving activity of whales. The heart rate-body mass measurements (35-24 bpm at body masses of 3,531-8,200 kg) in this study (1) extend the range of allometric heart rate and body mass data in mammals a full order of magnitude, to almost 10,000 kg, (2) support the use of allometric equations (based primarily on mammals <1,000 kg in body mass) in estimating resting heart rates in whales, and (3) demonstrate that previously reported heart rates in large whales are not representative of resting heart rate, probably secondary to circumstances during measurement.

Ponganis, PJ, Stockard TK, Meir JU, Williams CL, Ponganis KV, Van Dam RP, Howard R.  2007.  Returning on empty: extreme blood O-2 depletion underlies dive capacity of emperor penguins. Journal of Experimental Biology. 210:4279-4285.   10.1242/jeb.011221   AbstractWebsite

Blood gas analyses from emperor penguins (Aptenodytes forsteri) at rest, and intravascular P-O2 profiles from free-diving birds were obtained in order to examine hypoxemic tolerance and utilization of the blood O-2 store during dives. Analysis of blood samples from penguins at rest revealed arterial P(O2)s and O-2 contents of 68 +/- 7 mmHg (1 mmHg= 133.3 Pa) and 22.5 +/- 1.3 ml O-2 dl(-1) (N= 3) and venous values of 41 +/- 10 mmHg and 17.4 +/- 2.9 ml O-2 dl(-1) (N= 9). Corresponding arterial and venous Hb saturations for a hemoglobin (Hb) concentration of 18 g dl(-1) were > 91% and 70%, respectively. Analysis of P-O2 profiles obtained from birds equipped with intravascular P-O2 electrodes and backpack recorders during dives revealed that (1) the decline of the final blood P-O2 of a dive in relation to dive duration was variable, (2) final venous P-O2 values spanned a 40-mmHg range at the previously measured aerobic dive limit (ADL; dive duration associated with onset of post-dive blood lactate accumulation), (3) final arterial, venous and previously measured air sac P-O2 values were indistinguishable in longer dives, and (4) final venous P-O2 values of longer dives were as low as 1-6 mmHg during dives. Although blood O-2 is not depleted at the ADL, nearly complete depletion of the blood O-2 store occurs in longer dives. This extreme hypoxemic tolerance, which would be catastrophic in many birds and mammals, necessitates biochemical and molecular adaptations, including a shift in the O-2-Hb dissociation curve of the emperor penguin in comparison to those of most birds. A relatively higher-affinity Hb is consistent with blood P-O2 values and O-2 contents of penguins at rest.

Ponganis, PJ, Kooyman GL, Castellini MA.  1995.  Multiple sightings of Arnouxs beaked whales along the Victoria Land coast. Marine Mammal Science. 11:247-250.   10.1111/j.1748-7692.1995.tb00523.x   AbstractWebsite
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Ponganis, PJ, Kooyman GL, Zornow MH.  1991.  Cardiac output in swimming California sea lions, Zalophus californianus. Physiological Zoology. 64:1296-1306. AbstractWebsite

Cardiac output was determined by the thermodilution technique in three California sea lions while resting and while swimming. Metabolic rates increased seven-to ninefold above resting rates during maximal exercise. While the sea lions were at rest, stroke volume was also determined by simultaneously counting heart rate during cardiac output determinations. At rest, cardiac output (2.5-3.0 mL kg-1s-1) and stroke volume (2 mL kg-1) were similar to those of harbor seals and terrestrial mammals of similar mass. During exercise, mean cardiac output increased linearly with work load and surface/submerged intervals were short and frequent. The exercise capacity of swimming sea lions appears similar to that of harbor seals, but the exercise response resembles that of terrestrial mammals more than that of harbor seals.

Ponganis, PJ, Kooyman GL, Castellini MA.  1993.  Determinants of the aerobic dive limit of Weddell seals: analysis of diving metabolic rates, postdive end tidal PO2's, and blood and muscle oxygen stores. Physiological Zoology. 66:732-749. AbstractWebsite

The mean aerobic dive limit (ADL) for Weddell seals was calculated from data collected on diving metabolic rates (VO2) and blood and muscle O2 stores. Mean diving VO2 of adult seals during predominantly exploratory dive patterns was 4.5 mL O2 kg-1 min-1; mean VO2 of a subadult seal engaged in foraging dive bouts was 8.5 mL O2 kg-1 min-1. The adult value was 30% greater than that used in past ADL calculations. Mean plasma volume was 7% body mass (BM); blood volume calculated with the highest hematocrit (Hct) observed (66) was 21% BM. Hemoglobin concentration at such an Hct was 26% by weight. End tidal PO2 (pre- and postdive) justified the use of 95% and 20% arterial O2 saturations in the blood O2 store calculation. Total blood O2 stores were 50% greater than those used in past ADL calculations. Mean myoglobin concentration (5.4% by weight) and more recent anatomical estimates of muscle mass yielded a 35% increase in muscle O2 stores. The mean estimated ADL for a 450-kg seal calculated with these new data was 19.1 min, 2.3 min greater than in past calculations and only 1 min less than the 20-min inflection point of the curve of dive duration versus postdive lactic acid appearance. For the subadult engaged in foraging dives, the mean estimated ADL was about 9 min, again quite similar to past ADL calculations.

Ponganis, PJ, Kooyman GL.  1990.  Diving physiology of penguins. Acta XX Congressus Internationalis Ornithologici, Christchurch, New Zealand, 2-9 December 1990. ( Butler PJ, Jones DR, Eds.).:6., Wellington, N.Z.: New Zealand Ornithological Congress Trust Board Abstract
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Ponganis, PJ, Welch TJ, Welch LS, Stockard TK.  2010.  Myoglobin production in emperor penguins. Journal of Experimental Biology. 213:1901-1906.   10.1242/jeb.042093   AbstractWebsite

Increased oxygen storage is essential to the diving capacities of marine mammals and seabirds. However, the molecular mechanisms underlying this adaptation are unknown. Myoglobin (Mb) and Mb mRNA concentrations were analyzed in emperor penguin (Aptenodytes forsteri) adults and chicks with spectrophotometric and RNase protection assays to evaluate production of their large Mb-bound O(2) stores. Mean pectoral Mb concentration and Mb mRNA content increased throughout the pre-fledging period and were 15-fold and 3-fold greater, respectively, in adults than in 3.5 month old chicks. Mean Mb concentration in 5.9 month old juveniles was 2.7 +/- 0.4 g 100 g(-1) muscle (44% that of wild adults), and in adults that had been captive all their lives it was 3.7 +/- 0.1 g 100 g(-1) muscle. The Mb and Mb mRNA data are consistent with regulation of Mb production at the level of transcription as in other animals. Significant Mb and Mb mRNA production occurred in chicks and young juveniles even without any diving activity. The further increase in adult Mb concentrations appears to require the exercise/hypoxia of diving because Mb concentration in captive, non-diving adults only reached 60% of that of wild adults. The much greater relative increase in Mb concentration than in Mb mRNA content between young chicks and adults suggests that there is not a simple 1:1 relationship between Mb mRNA content and Mb concentration. Nutritional limitation in young chicks and post-transcriptional regulation of Mb concentration may also be involved.

Ponganis, PJ, Kooyman GL.  2000.  Diving physiology of birds: a history of studies on polar species. Comparative Biochemistry and Physiology a-Molecular and Integrative Physiology. 126:143-151.   10.1016/s1095-6433(00)00208-7   AbstractWebsite

Our knowledge of avian diving physiology has been based primarily on research with polar species. Since Scholander's 1940 monograph, research has expanded from examination of the 'diving reflex' to studies of free-diving birds, and has included laboratory investigations of oxygen stores, muscle adaptations, pressure effects, and cardiovascular/metabolic responses to swimming exercise. Behavioral and energetic studies at sea have shown that common diving durations of many avian species exceed the calculated aerobic diving limits (ADL). Current physiological research is focused on factors, such as heart rate and temperature, which potentially affect the diving metabolic rate and duration of aerobic diving. (C) 2000 Elsevier Science Inc. All rights reserved.

Ponganis, PJ, Kooyman GL, Starke LN, Kooyman CA, Kooyman TG.  1997.  Post-dive blood lactate concentrations in emperor penguins, Aptenodytes forsteri. Journal of Experimental Biology. 200:1623-1626. AbstractWebsite

In order to determine an aerobic diving limit (ADL) in emperor penguins (Aptenodytes forsteri), post-dive blood lactate concentrations were measured in penguins foraging at an isolated sea ice hole. Resting lactate concentrations were 1.2-2.7 mmol l(-1). Serial samples revealed that lactate level usually peaked within 5 min after dives and that 7-12 min was required for lactate concentrations to decrease from 5-8 mmol l(-1) to less than 2.5 mmol l(-1). Post-dive lactate level was not elevated above 3 mmol l(-1) for dives shorter than 5 min. Two-phase regression analysis revealed a transition at 5.6 min in the post-dive lactate level versus diving duration relationship. All dives longer than 7 min were associated with lactate concentrations greater than 5 mmol l(-1). We conclude that the ADL in emperor penguins ranges between 5 and 7 min. These are the first determinations of post-dive lactate concentrations in any free-diving bird and are currently the only physiological assessment of an ADL in an avian species.

Ponganis, PJ, Stockard TK, Levenson DH, Berg L, Baranov EA.  2006.  Intravascular pressure profiles in elephant seals: Hypotheses on the caval sphincter, extradural vein and venous return to the heart. Comparative Biochemistry and Physiology a-Molecular & Integrative Physiology. 145:123-130.   10.1016/j.cbpa.2006.05.012   AbstractWebsite

In order to evaluate bemodynamics in the complex vascular system of phocid seals, intravascular pressure profiles were measured during periods of rest-associated apnea in young elephant seals (Mirounga angustirostris). There were no significant differences between apneic and eupneic mean arterial pressures. During apnea, venous pressure profiles (pulmonary artery, thoracic portion of the vena cava (thoracic vena cava), extradural vein, and hepatic sinus) demonstrated only minor, transient fluctuations. During eupnea, all venous pressure profiles were dominated by respiratory fluctuations. During inspiration, pressures in the thoracic vena cava and extradural vein decreased -9 to -21 mm Hg, and -9 to -17 mm Hg, respectively. In contrast, hepatic sinus pressure increased 2-6 mm Hg during inspiration. Nearly constant hepatic sinus and intrathoracic vascular pressure profiles during the breath-hold period are consistent with incomplete constriction of the caval sphincter during these rest-associated apneas. During eupnea, negative inspiratory intravascular pressures in the chest ("the respiratory pump") should augment venous return via both the venae cavae and the extradural. vein. It is hypothesized that, in addition to the venae cavae, the prominent para-caval venous system of phocid seals (i.e., the extradural vein) is necessary to allow adequate venous return for maintenance of high cardiac outputs and blood pressure during eupnea. (c) 2006 Elsevier Inc. All rights reserved.

Ponganis, PJ, Kooyman GL, Van Dam R, Lemaho Y.  1999.  Physiological responses of king penguins during simulated diving to 136 m depth. Journal of Experimental Biology. 202:2819-2822. AbstractWebsite

To evaluate blood N-2 uptake and the role of the respiratory volume (air sacs/lungs) as a N-2 and O-2 reservoir in deep-diving penguins, diving respiratory volume (V-DR), heart rate (f(H)), venous P-N2, blood volume (V-b) and hemoglobin (Hb) concentration were measured in king penguins (Aptenodytes patagonicus) during forced submersions and compressions equivalent to depths up to 136 m, V-DR was 69+/-18 ml kg(-1) (mean +/- S.D.) in 62 submersions ranging from 4.4 atmospheres absolute (ATA; 1 ATA=101 kPa) (34 m) to 14.6 ATA (136 m), Submersion f(H) averaged 30+/-7 beats min(-1) (N=18), approximately 20% of pre- and post-submersion values. Venous P-N2 values during and after submersions as deep as 11.2 ATA (102 m) were all less than 2.8 atmospheres N-2 (283 kPa) above ambient pressure, a previously measured threshold for symptomatic bubble formation. Mean V-b was 83+/-8 ml kg(-1) (N=6); [Hb] was 17.6+/-0.7 g dl(-1) (N=7), On a mass-specific basis, mean V-DR, and therefore total available N-2, is 41% of that in shallow-diving penguin species. Total body O-2 stores, calculated from measured V-DR, V-b, [Hb], muscle mass and myoglobin concentration, are 45 ml kg(-1), with 23 % in the respiratory system. This small respiratory fraction in comparison with that in shallow-diving penguins suggests a lesser reliance on the respiratory oxygen store for extended breath-holding and also a reduced uptake of nitrogen at depth.

Ponganis, PJ.  2011.  Diving Mammals. Comprehensive Physiology. 1: John Wiley & Sons, Inc.   10.1002/cphy.c091003   AbstractWebsite

The ability of diving mammals to forage at depth on a breath hold of air is dependent on gas exchange, both in the lung and in peripheral tissues. Anatomical and physiological adaptations in the respiratory system, cardiovascular system, blood and peripheral tissues contribute to the remarkable breath-hold capacities of these animals. The end results of these adaptations include efficient ventilation, enhanced oxygen storage, regulated transport and delivery of respiratory gases, extreme hypoxemic/ischemic tolerance, and pressure tolerance. © 2011 American Physiological Society. Compr Physiol 1:447-465, 2011.

Ponganis, PJ, Van Dam RP, Knower T, Levenson DH.  2001.  Temperature regulation in emperor penguins foraging under sea ice. Comparative Biochemistry and Physiology a-Molecular and Integrative Physiology. 129:811-820.   10.1016/s1095-6433(01)00349-x   AbstractWebsite

Inferior vena caval (IVC) and anterior abdominal (AA) temperatures were recorded in seven emperor penguins (Aptenodytes foresteri) foraging under sea ice in order to evaluate the hypothesis that hypothermia-induced metabolic suppression might extend aerobic diving time. Diving durations ranged from 1 to 12.5 min, with 39% of dives greater than the measured aerobic dive limit of 5.6 min. Anterior abdominal temperature decreased progressively throughout dives, and partially returned to pre-dive values during surface intervals. The lowest AA temperature was 19 degreesC. However, mean AA temperatures during dives did not correlate with diving durations. In six of seven penguins, only minor fluctuations in IVC temperatures occurred during diving. These changes were often elevations in temperature. In the one exception, although IVC temperatures decreased, the reductions were less than those in the anterior abdomen and did not correlate with diving durations. Because of these findings, we consider it unlikely that regional hypothermia in emperor penguins leads to a significant reduction in oxygen consumption of the major organs within the abdominal core. Rather, temperature profiles during dives are consistent with a model of regional heterothermy with conservation of core temperature, peripheral vasoconstriction, and cooling of an outer body shell. (C) 2001 Elsevier Science Inc. All rights reserved.

Ponganis, PJ, McDonald BI, Tift MS, Williams CL.  2017.  Heart rate regulation in diving sea lions: the vagus nerve rules. Journal of Experimental Biology. 220:1372-1381.   10.1242/jeb.146779   AbstractWebsite

Recent publications have emphasized the potential generation of morbid cardiac arrhythmias secondary to autonomic conflict in diving marine mammals. Such conflict, as typified by cardiovascular responses to cold water immersion in humans, has been proposed to result from exercise-related activation of cardiac sympathetic fibers to increase heart rate, combined with depth-related changes in parasympathetic tone to decrease heart rate. After reviewing the marine mammal literature and evaluating heart rate profiles of diving California sea lions (Zalophus californianus), we present an alternative interpretation of heart rate regulation that de-emphasizes the concept of autonomic conflict and the risk of morbid arrhythmias in marine mammals. We hypothesize that: (1) both the sympathetic cardiac accelerator fibers and the peripheral sympathetic vasomotor fibers are activated during dives even without exercise, and their activities are elevated at the lowest heart rates in a dive when vasoconstriction is maximal, (2) in diving animals, parasympathetic cardiac tone via the vagus nerve dominates over sympathetic cardiac tone during all phases of the dive, thus producing the bradycardia, (3) adjustment in vagal activity, which may be affected by many inputs, including exercise, is the primary regulator of heart rate and heart rate fluctuations during diving, and (4) heart beat fluctuations (benign arrhythmias) are common in marine mammals. Consistent with the literature and with these hypotheses, we believe that the generation of morbid arrhythmias because of exercise or stress during dives is unlikely in marine mammals.

Ponganis, PJ.  2007.  Bio-logging of physiological parameters in higher marine vertebrates. Deep-Sea Research Part Ii-Topical Studies in Oceanography. 54:183-192.   10.1016/j.dsr2.2006.11.009   AbstractWebsite

Bio-logging of physiological parameters in higher marine vertebrates had its origins in the field of bio-telemetry in the 1960s and 1970s. The development of microprocessor technology allowed its first application to bio-logging investigations of Weddell seal diving physiology in the early 1980s. Since that time, with the use of increased memory capacity, new sensor technology, and novel data processing techniques, investigators have examined heart rate, temperature, swim speed, stroke frequency, stomach function (gastric pH and motility), heat flux, muscle oxygenation, respiratory rate, diving air volume, and oxygen partial pressure (PO(2)) during diving. Swim speed, heart rate, and body temperature have been the most commonly studied parameters. Bio-logging investigation of pressure effects has only been conducted with the use of blood samplers and nitrogen analyses on animals diving at isolated dive holes. The advantages/disadvantages and limitations of recording techniques, probe placement, calibration techniques, and study conditions are reviewed. (c) 2007 Elsevier Ltd. All rights reserved.

Ponganis, PJ, Kooyman GL, Castellini MA, Ponganis EP, Ponganis KV.  1993.  Muscle temperature and swim velocity profiles during diving in a Weddell seal, Leptonychotes weddellii. Journal of Experimental Biology. 183:341-346. AbstractWebsite

Locomotory muscle temperature and swim velocity profiles of an adult Weddell seal were recorded over a 21 h period. The highest temperatures occurred during a prolonged surface period (mean 37.3-degrees-C, S.D. 0.16-degrees-C). Muscle temperature averaged 36.8 and 36.6-degrees-C (S.D. 0.25-degrees-C, 0.19-degrees-C) during two dive bouts and showed no consistent fluctuations between dive and interdive surface intervals. Swim velocities were also constant, near 1.3 m s-1. These data indicate that past records of low aortic temperatures (35-degrees-C) during and after prolonged dives are not indicative of whole-body temperature changes, and that muscle temperature, even during dives as long as 45 min, remains near 37-degrees-C.