Physiology of diving of birds and mammals

1997 ◽  
Vol 77 (3) ◽  
pp. 837-899 ◽  
Author(s):  
P. J. Butler ◽  
D. R. Jones

This review concentrates on the physiological responses, and their control, in freely diving birds and mammals that enable them to remain submerged and sometimes quite active for extended periods of time. Recent developments in technology have provided much detailed information on the behavior of these fascinating animals. Unfortunately, the advances in technology have been insufficient to enable physiologists to obtain anything like the same level of detail on the metabolic rate and physiological adjustments that occur during natural diving. This has led to much speculation and calculations based on many assumptions concerning usable oxygen stores and metabolic rate during diving, in an attempt to explain the observed behavior. Despite their shortcomings, these calculations have provided useful insights into the degree of adaptations of various species of aquatic birds and mammals. Many of them, e.g., ducks, smaller penguins, fur seals, and Weddell seals, seem able to metabolize aerobically, when diving, at approximately the same (if not greater) rate as they do at the surface. Their enhanced oxygen stores are able to support aerobic metabolism, at what would not be considered unusually low levels, for the duration of the dives, although there are probably circulatory readjustments to ensure that the oxygen stores are managed judiciously. For other species, such as the larger penguins, South Georgian shag, and female elephant seals, there is a general consensus that they must either be reducing their aerobic metabolic rate when diving, possibly by way of regional hypothermia, and/or producing ATP, at least partly, by anaerobiosis and metabolizing the lactic acid when at the surface (although this is hardly likely in the case of the female elephant seals). Circulation is the proximate regulator of metabolism during aerobic diving, and heart rate is the best single indicator of circulatory adjustment. During voluntary dives, heart rates range from extreme bradycardia to well above resting, reflecting metabolic performance. Efferent cardiac control is largely parasympathetic. Reflex cardiorespiratory responses are modulated by conditioning and habituation, but reflexes predominate during extended dives and during recovery, when gas exchange is maximized.

2008 ◽  
Vol 20 (5) ◽  
pp. 425-435 ◽  
Author(s):  
Donald B. Siniff ◽  
Robert A. Garrott ◽  
Jay J. Rotella ◽  
William R. Fraser ◽  
David G. Ainley

AbstractWe consider how Antarctic seals may respond to changes in climate, realizing that anthropogenic alteration of food webs will influence these responses. The species considered include the ice-obligate - crabeater (Lobodon carcinophaga), Weddell (Leptonychotes weddellii), Ross (Ommataphoca rossii) and leopard (Hydrurga leptonyx) seal - and the ice-tolerant Antarctic fur seal (Arctocephalus gazella) and southern elephant seal (Mirounga leonina). The data analysed are from long-term censuses of Weddell seals in McMurdo Sound (1997–2006), and of Weddell, fur and elephant seals at Arthur Harbour, Antarctic Peninsula (1974–2005). After considering their responses to recent changes in environmental features, as well as projected and current changes to their habitat our conclusions are that the distribution and abundance of 1) crabeater and Weddell seals will be negatively affected by changes in the extent, persistence and type of annual sea ice, 2) Ross and leopard seal will be the least negatively influenced by changes in pack ice characteristics, although, as may be the case for crabeater and Weddell, population size and distribution may be altered through changes in food web dynamics, and 3) southern elephant and fur seals will respond in ways opposite to the pack ice species, but could also be influenced most immediately by changes in their food resources due to factors other than climate.


2018 ◽  
Vol 14 (7) ◽  
pp. 20180063 ◽  
Author(s):  
Andreas Ekström ◽  
Michael Axelsson ◽  
Albin Gräns ◽  
Jeroen Brijs ◽  
Erik Sandblom

Cardiac oxygenation is achieved via both coronary arterial and luminal venous oxygen supply routes in many fish species. However, the relative importance of these supplies for cardiac and aerobic metabolic performance is not fully understood. Here, we investigated how coronary artery ligation in rainbow trout ( Oncorhynchus mykiss ), implanted with heart rate loggers, affected cardiorespiratory performance in vivo . While coronary ligation significantly elevated resting heart rate, the standard metabolic rate was unchanged compared to sham-treated controls. However, coronary ligation reduced the maximum metabolic rate while heart rate remained unchanged following enforced exercise. Thus, coronary ligation reduced metabolic and heart rate scopes by 29% and 74%, respectively. Our findings highlight the importance of coronary oxygen supply for overall cardiorespiratory performance in salmonid fish, and suggest that pathological conditions that impair coronary flow (e.g. coronary arteriosclerosis) constrain the ability of fish to cope with metabolically demanding challenges such as spawning migrations and environmental warming.


1990 ◽  
Vol 259 (5) ◽  
pp. R1086-R1089 ◽  
Author(s):  
M. A. Castellini ◽  
D. P. Costa

Long-duration fasting in mammals can ultimately lead to stage three terminal starvation, which is characterized by depleted fat stores, a metabolic shift away from fat metabolism toward lean tissue catabolism, and a sharp decline in circulating levels of plasma fatty acids and ketone bodies. However, this biochemical shift has never been observed outside of the laboratory in a naturally fasting, nonhibernating mammal. In the current study, plasma levels of the ketone body D-beta-hydroxybutyrate (beta-HBA) were assayed in 10 Northern elephant seal pups during suckling and the postweaning fast and in 12 fasting adult seals. Plasma beta-HBA concentration in the pups was minimal during suckling (0.09 +/- 0.06 mM; n = 10) and began to increase immediately after weaning. The concentration rose until about 55 days into the fast (1.34 +/- 0.36 mM; n = 10) and then declined sharply. Within 10 days of this deflection point, the seal pups left for sea. By contrast, adult elephant seals showed consistently low levels of beta-HBA after several months of fasting (0.06 +/- 0.07 mM; n = 12). The data suggest that the duration of fasting in elephant seal pups may be determined, in part, by biochemical shifts that occur near the end of the fast and that the regulation of ketone concentration is different in fasting neonatal and adult elephant seals.


2020 ◽  
Vol 50 (4) ◽  
pp. 356-362
Author(s):  
Charlotte Sadler ◽  
◽  
Kaighley Brett ◽  
Aaron Heerboth ◽  
Austin R Swisher ◽  
...  

(Sadler C, Brett K, Heerboth A, Swisher AR, Mehregani N, Touriel R, Cannon DT. Safety proposals for freediving time limits should consider the metabolic-rate dependence of oxygen stores depletion. Diving and Hyperbaric Medicine. 2020 December 20;50(4):356–362. doi: 10.28920/dhm50.4.356-362. PMID: 33325016.) Introduction: There is no required training for breath-hold diving, making dissemination of safety protocols difficult. A recommended breath-hold dive time limit of 60 s was proposed for amateur divers. However, this does not consider the metabolic-rate dependence of oxygen stores depletion. We aimed to measure the effect of apnoea time and metabolic rate on arterial and tissue oxygenation. Methods: Fifty healthy participants (23 (SD 3) y, 22 women) completed four periods of apnoea for 60 s (or to tolerable limit) during rest and cycle ergometry at 20, 40, and 60 W. Apnoea was initiated after hyperventilation to achieve PETCO2 of approximately 25 mmHg. Pulse oximetry, frontal lobe oxygenation, and pulmonary gas exchange were measured throughout. We defined hypoxia as SpO2 < 88%. Results: Static and exercise (20, 40, 60 W) breath-hold break times were 57 (SD 7), 50 (11), 48 (11), and 46 (11) s (F [2.432, 119.2] = 32.0, P < 0.01). The rise in PETCO2 from initiation to breaking of apnoea was dependent on metabolic rate (time × metabolic rate interaction; F [3,147] = 38.6, P < 0.0001). The same was true for the fall in SpO2 (F [3,147] = 2.9, P = 0.03). SpO2 fell to < 88% on 14 occasions in eight participants, all of whom were asymptomatic. Conclusions: Independent of the added complexities of a fall in ambient pressure on ascent, the effect of apnoea time on hypoxia depends on the metabolic rate and is highly variable among individuals. Therefore, we contend that a universally recommended time limit for breath-hold diving or swimming is not useful to guarantee safety.


2002 ◽  
Vol 24 (2) ◽  
pp. 177 ◽  
Author(s):  
DM Spratt

This paper summarizes knowledge of the biodiversity and pathology associated with parasites of the respiratory tract of wild mammals, including feral species, in Australia. Representatives of 21 genera of nematodes distributed in the superfamilies Trichostrongyloidea, Metastrongyloidea, Thelazioidea, Filarioidea, Trichinelloidea and Muspiceoidea are included. Larval stages of the cestode, Echinococcus granulosus, occur in the lungs of macropodids and feral pigs (Sus scrofa). Trematodes occur in the lungs of dugongs (Dugong dugon) and in the cranial sinuses and blowholes of dolphins. Pentastomes occur in the lungs of the sugar glider (Petaurus breviceps) and in the frontal sinuses of dingoes (Canis lupus dingo) and foxes (Vulpes vulpes). Nymphal stages of the latter have been found in the lungs of rabbits (Oryctolagus cuniculus) and nymphs of a pentastome of tree pythons occur in the lungs of the northern brown bandicoot (Isoodon macrourus). Pneumonyssid mites occur in the lungs of the northern brushtail possum (Trichosurus vulpecula arnhemensis) and an undescribed speleognathine mite has been found in the lungs of P. breviceps. Trombiculid, tydeoid, dermanyssid and halarachnid mites are endoparasitic in the nasal sinuses of rodents, antechinuses, possums, gliders, elephant seals and fur seals. Larvae of oestrid bot-flies occur in the trachea of macropodids and in the nasal sinuses of camels (Camelus dromedarius). Host specificity in these parasites represents the full spectrum from species specific to class catholic with the intranasal chigger, Ascoschoengastia rattus, occuring in metatherian and eutherian mammals as well as varanid lizards. Similarly, pathological changes associated with these parasites range from inapparent to verminous bronchitis and bronchiolitis resulting in mortalities or severely impaired respiratory reserve or hypoxia precipitating death.


1959 ◽  
Vol 37 (3) ◽  
pp. 473-478 ◽  
Author(s):  
O. Héroux ◽  
F. Depocas ◽  
J. S. Hart

Physiological adjustments to cold temperature have been compared in white rats exposed either to the outdoor fluctuating environmental conditions or to the indoor constant temperature conditions. While the metabolic adjustments such as increased peak metabolism and decreased shivering were similar in outdoor and indoor rats exposed to cold, the adjustments in insulation and thermoneutral metabolic rates were quite different. The pelage insulation increased in the rats kept outside during the winter but remained unchanged in the rats kept in a constant temperature room maintained at 6 °C. The resting metabolic rate measured at 30 °C increased in the 6 °C acclimated rats but not in the winter-exposed animals. Over the temperature range +30 °C to −15 °C, while the indoor cold-acclimated rats had a higher metabolic rate than their controls acclimated to 30 °C, the winter rats had a lower metabolism than their summer controls.


Sign in / Sign up

Export Citation Format

Share Document