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  • 1
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Dolphins-Physiology. ; Bottlenose dolphins. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (304 pages)
    Edition: 1st ed.
    ISBN: 9780323905176
    DDC: 573.89195
    Language: English
    Note: Intro -- The Physiology of Dolphins -- Copyright -- Dedication -- Contents -- Contributors -- Acknowledgments -- Chapter 1: Studying dolphin physiology -- The bottlenose dolphin -- Studies of stranded animals -- Studies of animals under human care -- Field studies of wild animals -- Animal-attached instrumentation -- Anatomy and physiology -- This book -- References -- Chapter 2: Energetic costs of rest and locomotion in dolphins -- Introduction -- Resting metabolic rate: An energetic baseline for aquatic living -- Predicting resting metabolic rate of dolphins and other mammals -- Resting metabolic rate of dolphins and other marine mammals -- Special consideration of RMR in large whales -- Energetic costs of swimming and diving -- Relationships between hydrodynamics, speed, and energetics -- The high cost of speed -- Cost of transport -- Conservation of energy through drafting, gliding, and leaping -- Energetic limits: Aerobic scope and VO2max -- Predicting free-ranging locomotory costs -- Accelerometry and energetics in the wild -- Field metabolic rates -- Concluding remarks -- References -- Chapter 3: Thermoregulation -- Introduction -- Avenues of heat transfer -- Thermal adaptations span morphology, physiology, and behavior -- The role of size and morphology -- Bergmann's and Allen's rules -- Appendages as thermal windows: Where morphology and physiology meet -- Thermal effects of exercise and diving -- Blubber structure and its thermoregulatory function -- Intrinsic and extrinsic factors affecting blubber -- Blubber's dynamic role in thermoregulation -- Thermoregulatory considerations for epidermal growth and repair -- Energetic tradeoffs with thermoregulation -- Concluding remarks -- References -- Chapter 4: Muscles and movement -- Introduction -- Streamlining -- Fusiform body design -- Control surfaces -- Propulsive fluke design. , Fluke internal structure -- Propulsive muscles and tendons -- Speed -- Hydrodynamics -- Drag -- Drag reduction mechanisms -- Swimming kinematics -- Up/downstroke -- Thrust generation -- Control of pitch angle -- Propulsive efficiency -- Flexibility and spring-like effects -- Scaling -- Behavioral strategies for energy economy -- Submerged swimming -- Porpoising -- Gliding -- Bow riding -- Wave riding -- Drafting -- Maneuverability -- References -- Chapter 5: Cardiovascular physiology in dolphins and other cetaceans -- Cardiovascular anatomy and function -- Heart-Anatomy -- Heart size -- Hemodynamics: Cardiac output and stroke volume -- Hemodynamics: Heart function and blood pressure -- The vasculature -- Aorta -- Retia mirabilia -- Venous plexuses and epidural veins -- Posterior vena caval hemodynamics during fluking -- Cardiovascular function during diving -- The dive response -- Early studies of heart rates in small- and medium-sized cetaceans -- Heart rate profiles during diving -- Heart rate profiles during postdive intervals and during high-speed surface travel -- Heart rate and oxygen store management -- Blood O2 transport -- Hemoglobin concentration -- O2-Hb dissociation curves -- Summary -- References -- Chapter 6: Respiratory physiology in the dolphin and other whales -- Introduction -- Function of the respiratory system -- Volumes of the respiratory system -- Respiratory mechanics -- Anatomy and structure -- Air flow pathway and branching pattern -- The lung -- Larynx and trachea -- Bronchial airways -- Alveolar structures -- Functional studies in dead animals -- Excised tissue -- Cadavers -- Functional studies in live animals -- Lung function testing in live cetaceans -- Minimum air volume, residual volume, and total lung capacity -- Respiratory flow -- The lungs and pressure -- Lung function testing and respiratory health. , Future possibilities -- References -- Chapter 7: Diving physiology in dolphins and human -- Introduction to diving physiology -- A dolphin perspective -- A human perspective -- The dive response -- Overview -- Facial receptors and cardiovascular responses -- Blood pressure -- Splenic contraction -- Comparative perspectives of the diving response -- Cognitive control over bradycardia -- Hypoxia and acid-base disturbance -- Blood gases in humans -- Blood gases in dolphins -- Involuntary breathing movements -- Loss of consciousness: Hypoxic syncope or shallow-water blackout -- Pressure effects -- Risk of pulmonary barotrauma -- Risk of nitrogen narcosis -- Risk of decompression sickness -- Other considerations to minimize metabolic rate -- Conclusion -- References -- Chapter 8: Genetic and molecular adaptations -- Introduction -- From genotype to phenotype -- DNA-level mechanisms -- Gene gain/loss -- Gene mutations -- Gene regulatory networks -- RNA-level mechanisms -- Protein-level mechanisms -- Adaptations to the marine environment -- Unique molecular features of marine mammals -- Thermoregulation -- Locomotion -- Sensory -- Diving -- Future directions -- Leveraging natural experiments -- Functional studies: Physiology meets genomics -- References -- Chapter 9: Neurophysiology -- Histology -- Cell types, their shape, and dimensions -- Neural density -- Shape and volume of the brain -- Shape of the brain -- Brain mass -- The encephalization quotient and comparison with other mammals -- The cerebral cortex of whales and dolphins -- The corpus callosum, cerebral ventricles, and blood-brain barrier -- Organization of the cetacean cortical column and analogies with other mammals -- Projections from the thalamus and different organization of the cortical column -- Cerebral topography -- The cerebellum, the brainstem, and the spinal cord. , Relevant differences with terrestrial mammals -- The spinal cord -- Motor systems -- Motor cortex and control of body movement -- Prevalence of the extrapyramidal system -- Blood supply -- The internal carotid system -- The spinal and thoracic retia mirabilia -- Vascular shunts and the theory of the half-brain -- Functional organization of the cetacean central nervous system -- Limits to research -- Anatomical techniques -- Studies based on anatomical dissections, serial sections, and tracing -- Role of magnetic resonance imaging studies -- Studies based on diffusion tensor imaging -- The role of cranial nerves -- Physiological techniques -- Studies based on electrophysiology -- Electroencephalogram and related techniques -- fNIRS studies -- Modern studies based on behavioral experiments -- The diving brain -- The central nervous system and diving -- The effects of pressure on the brain -- Decompression sickness, nitrogen narcosis, and oxygen toxicity -- Thermoregulation and the development of the cetacean brain -- The unknowns of the cetacean nervous system -- The development of the cetacean brain -- The question of body size -- Opinionated studies -- Chemoreception: Olfaction -- Perception of environmental pressure and deep diving -- Neuro-hormonal control of circadian and circannual rhythmicity -- The organization of the five (or four or even three) layered cortex -- The question of the magnetic sense -- Differential vascularization of selected brain areas -- Brain metabolism and the long and deep dives -- Delphinid language -- Conclusion -- References -- Chapter 10: Sensory physiology in delphinids -- Introduction -- Vision -- Specifics of the eye globe, its position, and mobility -- The dioptric apparatus and the iris -- The retina and visual function -- Mechanoreception -- Hearing -- Auditory anatomy -- Hearing abilities. , Automatic gain control -- Noise impacts -- Touch and hydrodynamics -- Electroreception -- Chemosensation -- Olfaction -- Gustation -- Conclusions -- References -- Chapter 11: Kidneys and osmoregulation -- Introduction -- Kidney structure -- Urine concentration and kidney function -- Do dolphins drink salt water? -- Feeding and fasting studies -- Loading experiments -- Renal endocrinology of dolphins -- Renal pathologies and toxicology -- Summary -- References -- Chapter 12: Reproductive physiology of dolphins -- Introduction -- Onset of sexual maturation -- Reproductive cycles -- Gestation and lactation -- Reproductive anomalies and abnormalities -- Pseudopregnancy -- Spontaneous abortions, dystocia, perinatal loss, and failure to thrive -- Contraception and assisted reproductive technologies -- Contraception -- Assisted reproductive technologies -- External impacts on reproduction -- Ex-situ conservation applications -- References -- Chapter 13: Immunology -- Introduction to immunology -- Recent progress in cetacean immunology -- Anatomy and histology of immune organs -- Innate immunity -- Innate immune cells -- Cell activation -- Phagocytosis -- Respiratory burst -- Natural killer cell activity -- Acquired immunity -- Immune cells and their subsets -- Cytokines -- Lymphocyte activation and proliferation -- Humoral immune response -- Cellular immune response -- Inflammation -- Other tools -- Immunology and stress -- The connection between the nervous and immune systems -- Stressors and marine mammals -- Studies of the nervous and immune systems in cetaceans under professional human care -- Capture-release studies of cetaceans -- Cetacean strandings -- Monitoring stress and the immune system in free-ranging cetaceans -- Immunology and diving physiology -- Pressure -- Temperature -- Hypoxia/reperfusion -- Mammalian dive response. , Cellular adaptations to diving in marine mammals.
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  • 2
    ISSN: 1432-2013
    Keywords: Hydrogen diving Hyperbaria Thermoregulation Hydrogen narcosis HPNS
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. We used direct calorimetry and respirometry to measure the total rate of heat loss (Q Σ) and of oxygen consumption ( $$ \mathop V\limits^ \bullet {\rm O}_{\rm 2} $$ ) in guinea pigs in 1-atm (0.1 MPa) air and at 10–60 atm in either heliox (98% He, 2% O2) or hydrox (98% H2, 2% O2). Our objective was to determine if the physiological responses to these two gas mixtures were different and, if so, whether the differences were attributable to the thermal characteristics of the gases alone or were confounded by additional mechanisms. At 10–40 atm, Q Σ and $$ \mathop V\limits^ \bullet {\rm O}_{\rm 2} $$ were not significantly different in the two gas mixtures, whereas at 60 atm, Q Σ and $$ \mathop V\limits^ \bullet {\rm O}_{\rm 2} $$ were significantly higher in heliox than in hydrox. The $$ \mathop V\limits^ \bullet {\rm O}_{\rm 2} /Q_{\rm \Sigma } $$ ratio suggested that the animals were not in thermal equilibrium in hyperbaria. Based solely on the differing thermal properties of the gas mixtures, a mathematical model predicted a Q Σ that was higher in hydrox than in heliox at all pressures. Two plausible explanations are suggested: one is an adaptive lowering of the surface temperature as a physiological response of the animal to the thermally more stressful hydrox environment, and the other is related to the narcotic suppression of the animal's activity by hydrox.
    Type of Medium: Electronic Resource
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  • 3
    Publication Date: 2023-02-08
    Description: It is fundamentally important for many animal ecologists to quantify the costs of animal activities, although it is not straightforward to do so. The recording of triaxial acceleration by animal-attached devices has been proposed as a way forward for this, with the specific suggestion that dynamic body acceleration (DBA) be used as a proxy for movement-based power. Dynamic body acceleration has now been validated frequently, both in the laboratory and in the field, although the literature still shows that some aspects of DBA theory and practice are misunderstood. Here, we examine the theory behind DBA and employ modelling approaches to assess factors that affect the link between DBA and energy expenditure, from the deployment of the tag, through to the calibration of DBA with energy use in laboratory and field settings. Using data from a range of species and movement modes, we illustrate that vectorial and additive DBA metrics are proportional to each other. Either can be used as a proxy for energy and summed to estimate total energy expended over a given period, or divided by time to give a proxy for movement-related metabolic power. Nonetheless, we highlight how the ability of DBA to predict metabolic rate declines as the contribution of non-movement-related factors, such as heat production, increases. Overall, DBA seems to be a substantive proxy for movement-based power but consideration of other movement-related metrics, such as the static body acceleration and the rate of change of body pitch and roll, may enable researchers to refine movement-based metabolic costs, particularly in animals where movement is not characterized by marked changes in body acceleration.
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
    Format: text
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  • 4
    Publication Date: 2023-02-08
    Description: Vertebrates are recognized as sentient beings. Consequently, urgent priority is now being given to understanding the needs and maximizing the welfare of animals under human care. The general health of animals is most commonly determined by physiological indices e.g., blood sampling, but may also be assessed by documenting behavior. Physiological health assessments, although powerful, may be stressful for animals, time-consuming and costly, while assessments of behavior can also be time-consuming, subject to bias and suffer from a poorly defined link between behavior and health. However, behavior is recognized as having the potential to code for stress and well-being and could, therefore, be used as an indicator of health, particularly if the process of quantifying behavior could be objective, formalized and streamlined to be time efficient. This study used Daily Diaries (DDs) (motion-sensitive tags containing tri-axial accelerometers and magnetometers), to examine aspects of the behavior of bycaught loggerhead turtles, Caretta caretta in various states of health. Although sample size limited statistical analysis, significant behavioral differences (in terms of activity level and turn rate) were found between “healthy” turtles and those with external injuries to the flippers and carapace. Furthermore, data visualization (spherical plots) clearly showed atypical orientation behavior in individuals suffering gas emboli and intestinal gas, without complex data analysis. Consequently, we propose that the use of motion-sensitive tags could aid diagnosis and inform follow-up treatment, thus facilitating the rehabilitation process. This is particularly relevant given the numerous rehabilitation programs for bycatch sea turtles in operation. In time, tag-derived behavioral biomarkers, TDBBs for health could be established for other species with more complex behavioral repertoires such as cetaceans and pinnipeds which also require rehabilitation and release. Furthermore, motion-sensitive data from animals under human care and wild conspecifics could be compared in order to define a set of objective behavioral states (including activity levels) for numerous species housed in zoos and aquaria and/or wild species to help maximize their welfare.
    Type: Article , PeerReviewed
    Format: text
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  • 5
    Publication Date: 2024-04-19
    Description: Understanding the behavioural ecology of endangered taxa can inform conservation strategies. The activity budgets of the loggerhead turtle Caretta caretta are still poorly understood because many tracking methods show only horizontal displacement and ignore dives and associated behaviours. However, time-depth recorders have enabled researchers to identify flat, U-shaped dives (or type 1a dives) and these are conventionally labelled as resting dives on the seabed because they involve no vertical displacement of the animal. Video- and acceleration-based studies have demonstrated this is not always true. Focusing on sea turtles nesting on the Cabo Verde archipelago, we describe a new metric derived from magnetometer data, absolute angular velocity, that integrates indices of angular rotation in the horizontal plane to infer activity. Using this metric, we evaluated the variation in putative resting behaviours during the bottom phase of type 1a dives for 5 individuals over 13 to 17 d at sea during a single inter-nesting interval (over 75 turtle d in total). We defined absolute resting within the bottom phase of type 1a dives as periods with no discernible acceleration or angular movement. Whilst absolute resting constituted a significant proportion of each turtle’s time budget for this 1a dive type, turtles allocated 16−38% of their bottom time to activity, with many dives being episodic, comprised of intermittent bouts of rest and rotational activity. This implies that previously considered resting behaviours are complex and need to be accounted for in energy budgets, particularly since energy budgets may impact conservation strategies. © The authors 2021. Open Access under Creative Commons by Attribution Licence. Use, distribution and reproduction are unrestricted. Authors and original publication must be credited
    Type: Article , PeerReviewed
    Format: text
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  • 6
    Publication Date: 2022-05-25
    Description: © The Author(s), 2011. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Proceedings of the Royal Society B : Biological Sciences 279 (2012): 1396-1404, doi:10.1098/rspb.2011.1754.
    Description: Bubbles in supersaturated tissues and blood occur in beaked whales stranded near sonar exercises, and post-mortem in dolphins bycaught at depth and then hauled to the surface. To evaluate live dolphins for bubbles, liver, kidneys, eyes and blubber–muscle interface of live-stranded and capture-release dolphins were scanned with B-mode ultrasound. Gas was identified in kidneys of 21 of 22 live-stranded dolphins and in the hepatic portal vasculature of 2 of 22. Nine then died or were euthanized and bubble presence corroborated by computer tomography and necropsy, 13 were released of which all but two did not re-strand. Bubbles were not detected in 20 live wild dolphins examined during health assessments in shallow water. Off-gassing of supersaturated blood and tissues was the most probable origin for the gas bubbles. In contrast to marine mammals repeatedly diving in the wild, stranded animals are unable to recompress by diving, and thus may retain bubbles. Since the majority of beached dolphins released did not re-strand it also suggests that minor bubble formation is tolerated and will not lead to clinically significant decompression sickness.
    Description: Funding for this work was provided by the US Office of Naval Research Award no. N000140811220 and the International Fund for Animal Welfare.
    Keywords: Stranding ; Decompression sickness ; Gas bubbles ; Diving physiology ; Marine mammals
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: application/pdf
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  • 7
    Publication Date: 2022-05-25
    Description: © The Author(s), 2011. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Proceedings of the Royal Society B Biological Sciences 279 (2012): 1041-1050, doi:10.1098/rspb.2011.2088.
    Description: Decompression sickness (DCS; ‘the bends’) is a disease associated with gas uptake at pressure. The basic pathology and cause are relatively well known to human divers. Breath-hold diving marine mammals were thought to be relatively immune to DCS owing to multiple anatomical, physiological and behavioural adaptations that reduce nitrogen gas (N2) loading during dives. However, recent observations have shown that gas bubbles may form and tissue injury may occur in marine mammals under certain circumstances. Gas kinetic models based on measured time-depth profiles further suggest the potential occurrence of high blood and tissue N2 tensions. We review evidence for gas-bubble incidence in marine mammal tissues and discuss the theory behind gas loading and bubble formation. We suggest that diving mammals vary their physiological responses according to multiple stressors, and that the perspective on marine mammal diving physiology should change from simply minimizing N2 loading to management of the N2 load. This suggests several avenues for further study, ranging from the effects of gas bubbles at molecular, cellular and organ function levels, to comparative studies relating the presence/absence of gas bubbles to diving behaviour. Technological advances in imaging and remote instrumentation are likely to advance this field in coming years.
    Description: This paper and the workshop it stemmed from were funded by the Woods Hole Oceanographic Institution Marine Mammal Centre.
    Keywords: Diving physiology ; Marine mammals ; Gas bubbles ; Embolism ; Decompression sickness
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: application/pdf
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  • 8
    Publication Date: 2022-05-25
    Description: © The Author(s), 2012. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Frontiers in Physiology 3 (2012): 125, doi:10.3389/fphys.2012.00125.
    Description: Naval sonar has been accused of causing whale stranding by a mechanism which increases formation of tissue N2 gas bubbles. Increased tissue and blood N2 levels, and thereby increased risk of decompression sickness (DCS), is thought to result from changes in behavior or physiological responses during diving. Previous theoretical studies have used hypothetical sonar-induced changes in both behavior and physiology to model blood and tissue N2 tension (PN2), but this is the first attempt to estimate the changes during actual behavioral responses to sonar. We used an existing mathematical model to estimate blood and tissue N2 tension (PN2) from dive data recorded from sperm, killer, long-finned pilot, Blainville’s beaked, and Cuvier’s beaked whales before and during exposure to Low- (1–2 kHz) and Mid- (2–7 kHz) frequency active sonar. Our objectives were: (1) to determine if differences in dive behavior affects risk of bubble formation, and if (2) behavioral- or (3) physiological responses to sonar are plausible risk factors. Our results suggest that all species have natural high N2 levels, with deep diving generally resulting in higher end-dive PN2 as compared with shallow diving. Sonar exposure caused some changes in dive behavior in both killer whales, pilot whales and beaked whales, but this did not lead to any increased risk of DCS. However, in three of eight exposure session with sperm whales, the animal changed to shallower diving, and in all these cases this seem to result in an increased risk of DCS, although risk was still within the normal risk range of this species. When a hypothetical removal of the normal dive response (bradycardia and peripheral vasoconstriction), was added to the behavioral response during model simulations, this led to an increased variance in the estimated end-dive N2 levels, but no consistent change of risk. In conclusion, we cannot rule out the possibility that a combination of behavioral and physiological responses to sonar have the potential to alter the blood and tissue end-dive N2 tension to levels which could cause DCS and formation of in vivo bubbles, but the actually observed behavioral responses of cetaceans to sonar in our study, do not imply any significantly increased risk of DCS.
    Description: This study was funded by the Norwegian Ministry of Defence, US-Office of Naval Research, the Netherlands Ministry of Defence, the Norwegian Research Council and WWF-Norway.
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 9
    Publication Date: 2022-05-25
    Description: Author Posting. © The Author(s), 2011. This is the author's version of the work. It is posted here by permission of The Company of Biologists for personal use, not for redistribution. The definitive version was published in Journal of Experimental Biology 214 (2011): 3822-3828, doi:10.1242/jeb.056366.
    Description: Excised lungs from 8 marine mammal species (harp [Pagophilus groenlandicus], harbor [Phoca vitulina], and gray seal [Halichoerus grypus], Atlantic white-sided [Lagenorhynchus acutus], common [Delphinus delphis] and Risso's dolphin [Grampus griseus], long finned pilot whale [Globicephala melas], and harbor porpoise [Phocoena phocoena]) were used to determine minimum air volume of the relaxed lung (MAV, n = 15) and the elastic properties (pressure-volume curves, n = 24) of the respiratory system, and total lung capacity (TLC). Our data indicate that mass-specific TLC (sTLC, l • kg-1) does not differ between species or groups (odontocete vs. phocid) and agree with that estimated (TLCest) from body mass (Mb) by: TLCest = 0.135 • Mb 0.92. Measured MAV was on average 7% of TLC, with a range from 0% to 16%. The pressure-volume curves were similar among species on inflation but diverged during deflation in phocids as compared with odontocetes. These differences provide a structural basis for observed species differences in depth at which lungs collapse and gas exchange ceases.
    Description: This project was supported by a grant from the Office of Naval Research (ONR award number N00014-10-1-0059; Dr. Loring was supported by HL 52586 from the National Institutes of Health.
    Description: 2012-11-15
    Keywords: Lung mechanics ; Total lung capacity ; Minimum air volume ; Excised lung ; Diving physiology
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
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  • 10
    Publication Date: 2022-05-25
    Description: Author Posting. © Company of Biologists, 2017. This article is posted here by permission of Company of Biologists for personal use, not for redistribution. The definitive version was published in Journal of Experimental Biology 220 (2017): 1761-1773, doi:10.1242/jeb.126870.
    Description: In this Review, we focus on the functional properties of the respiratory system of pinnipeds and cetaceans, and briefly summarize the underlying anatomy; in doing so, we provide an overview of what is currently known about their respiratory physiology and mechanics. While exposure to high pressure is a common challenge among breath-hold divers, there is a large variation in respiratory anatomy, function and capacity between species – how are these traits adapted to allow the animals to withstand the physiological challenges faced during dives? The ultra-deep diving feats of some marine mammals defy our current understanding of respiratory physiology and lung mechanics. These animals cope daily with lung compression, alveolar collapse, transient hyperoxia and extreme hypoxia. By improving our understanding of respiratory physiology under these conditions, we will be better able to define the physiological constraints imposed on these animals, and how these limitations may affect the survival of marine mammals in a changing environment. Many of the respiratory traits to survive exposure to an extreme environment may inspire novel treatments for a variety of respiratory problems in humans.
    Description: Funding for this project was provided by the Office of Naval Research (ONR YIP Award no. N000141410563).
    Description: 2018-05-17
    Keywords: Compliance ; Marine mammal ; Lung function ; Respiratory flow ; Tidal volume ; Residual volume ; Total lung capacity ; Respiratory frequency ; Alveolar collapse
    Repository Name: Woods Hole Open Access Server
    Type: Article
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