PubMed Health⌕ Search

SEARCH · PubMed Health

Results for “Diving physiology”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 109 records · Page 6Linked to original sources

Pulmonary atelectasis formation during diving with closed-circuit oxygen breathing apparatus.

The physiological effects of diving with two types of closed-circuit oxygen breathing apparatus were investigated in 4 divers. In one apparatus the breathing bag was mounted on the dorsum and in the other on the chest, inducing -2 kPa and +1 to +2 kPa static lung load in the prone position, respectively. The back-mounted bag caused an unfavorable swimming position, with increased heart rate, breathing rate, and rating of perceived exertion (RPE) for work load. The greater internal and external work of breathing (the latter judged from the higher RPE for breathing resistance) probably contributed to a higher RPE for discomfort with the back-mounted bag. Three divers showed great reduction in vital capacity (VC) (0.8 to 1.9 liters) and developed coughing attacks after dives with this apparatus; these results were interpreted as possible indications of atelectasis formation. The 4th diver showed slight reduction in VC with both types of bag, possibly because the changes in static lung loads did not influence the airway closure in this man.

Adult↗

Metabolic limits on dive duration and swimming speed in the southern elephant seal Mirounga leonina.

The ability of air-breathing marine predators to forage successfully depends on their ability to remain submerged. This is in turn related to their total O(2) stores and the rate at which these stores are used up while submerged. Body size was positively related to dive duration in a sample of 34 adult female southern elephant seals from Macquarie Island. However, there was no relationship between body size and dive depth. This indicates that smaller seals, with smaller total O(2) stores, make shorter dives than larger individuals but operate at similar depths, resulting in less time being spent at depth. Nine adult female elephant seals were also equipped with velocity time depth recorders. In eight of these seals, a plot of swimming speed against dive duration revealed a cloud of points with a clear upper boundary. This boundary could be described using regression analysis and gave a significant negative relationship in most cases. These results indicate that metabolic rate varies with activity levels, as indicated by swimming speed, and that there are quantifiable limits to the distance that a seal can travel on a dive of a given swimming speed. However, the seals rarely dive to these physiological limits, and the majority of their dives are well within their aerobic capacity. Elephant seals therefore appear to dive in a way that ensures that they have a reserve of O(2) available.

Aerobiosis↗

Energetics of diving in macaroni penguins.

Heart rate (fH), abdominal temperature (T(ab)) and diving depth were measured in thirteen free-ranging breeding female macaroni penguins. Measurement of these variables allowed estimation of the mass-specific rate of oxygen consumption (V(O(2))) while diving and investigation of the physiological adjustments that might facilitate the diving behaviour observed in this species. In common with other diving birds, macaroni penguins showed significant changes in fH associated with diving, and these variables accounted for 36% of the variation in dive duration. When V(O(2)) was calculated for dives of different durations, 95.3% of dives measured were within the calculated aerobic dive limit (cADL) for this species. Mean fH for all complete dive cycles was 147+/-6 beats min(-1). When this fH is used to estimate (O(2)) of 26.2+/-1.4 ml min(-1) kg(-1) then only 92.8% of dives measured were within the cADL. Significant changes in abdominal temperature were not detected within individual dives, though the time constant of the measuring device used may not have been low enough to record these changes if they were present. Abdominal temperature did decline consistently during bouts of repeated diving of all durations and the mean decrease in T(ab) during a diving bout was 2.32+/-0.2 degrees C. There was a linear relationship between bout duration and the magnitude of this temperature drop. There was no commensurate increase in dive duration during dive bouts as T(ab) declined, suggesting that macaroni penguins are diving within their physiological limits and that factors other than T(ab) are important in determining the duration of dives and dive bouts. Lowered T(ab) will in turn facilitate lower metabolic rates during diving bouts, but it was not possible in the present study to determine the importance of this energy saving and whether it is occurs actively or passively.

Aerobiosis↗

The conduct of metabolic balances during simulated deep dives.

Metabolic balance studies were carried out during a series of simulated deep saturation dives at a Government Research Laboratory at which the physiology of deep diving is under investigation. The methodology employed in controlling diets in the hyperbaric helium-oxygen atmosphere is described in detail. The discussion covers two main areas: dietary problems - including anorexia, changes in taste and food texture - and physiological effects - including nausea and high pressure nervous syndrome (HPNS).

Atmosphere Exposure Chambers↗

The effect of myoglobin concentration on aerobic dive limit in a Weddell seal.

One physiological adaptation for prolonged dive duration in marine mammals is an elevated myoglobin (Mb) concentration in skeletal muscle. To determine the influence of Mb concentration on the aerobic dive limit (ADL), we modified a previously published model that simulated aerobic dives in a Weddell seal (Leptonychotes weddellii) and ran it for four Mb concentrations: 5, 27, 54 and 108 g Mb kg(-1) muscle representing 7%, 50%, 100% and 200%, respectively, of the normal Mb concentration in Weddell seal skeletal muscle. The model was run at increasing levels of muscular exertion and under postabsorptive and postprandial conditions to determine their effect on ADL. For each set of conditions, the model was also run at different levels of cardiac output (i.e. the dive response was varied) to determine the level of convective oxygen transport that optimized the ADL. In a postabsorptive state at a routine level of muscular exertion for a diving Weddell seal, a decrease in Mb concentration to 7% of normal caused a 39% decrease in the ADL (18 min to 11 min), while doubling the Mb concentration increased the ADL by 30% (18 min to 24 min). Under postprandial conditions at a routine level of muscular exertion, doubling the Mb concentration did not increase the ADL (12 min). The convective oxygen transport needed to meet the metabolic demands (Heat Increment of Feeding, HIF) of the splanchnic organs during digestion and assimilation required a cardiac output that was not optimal for the efficient use of muscle oxygen stores. This resulted in an over perfusion of the muscles and incomplete use of myoglobin-bound oxygen. As a result, the postprandial ADL was limited by the amount of oxygen stored in the blood, and increasing the Mb concentration had no effect on the ADL. We hypothesize that myoglobin concentration is optimized for the type and duration of dives routinely made by Weddell seals, and that a further increase may not increase the ADL for most free-ranging dives.

Animals↗

Asthma and the diver.

Self-contained underwater breathing apparatus (scuba) diving has grown in popularity, with nearly 9 million sport divers in the United States alone. Approximately 7% of the population has been diagnosed with asthma, which is similar to the percentage of divers admitting they have asthma. Numerous concerns exist regarding subjects with asthma who choose to participate in recreational diving. Among these concerns are pulmonary barotrauma, pneumomediastinum, pneumothorax, arterial gas embolism, ear barotrauma, sinus barotrauma, and dental barotrauma. Despite these concerns, a paucity of information exists linking asthma to increased risk of diving complications. However, it has long been the norm to discourage individuals with asthma from participating in recreational scuba diving. This article examines the currently available literature to allow for a more informed decision regarding the possible risks associated with diving and asthma. It examines the underlying physiological principles associated with diving, including Henry's law and Boyle's law, to provide a more intimate understanding on physiological changes occurring in the respiratory system under compressive stress. Finally, this article offers a framework for guiding the patient with asthma who is interested in scuba diving. Under the right circumstances, the patient with asthma can safely participate in recreational diving without apparent increased risk of an asthma-related event.

Asthma↗

Cardiovascular adjustments to laboratory diving in beavers and nutria.

Beavers (Castor canadensis) and nutria (Myocastor coypus) were anesthetized with halothane and catheters placed in the left ventricle, aorta and pulmonary artery, right ventricle or right atrium. The animals were strapped to a board and following recovery from anesthesia the following measurements were taken: regional distribution of blood flow, cardiac output, O2 consumption, arterial and venous blood gases, and pH. The animal was then immersed in 15-20 degrees C water for up to 2.75 min (nutria) or 4 min (beaver) and the measurements repeated. Heart rate and cardiac output decreased by 80 and 75%, respectively. Arterial and venous oxygen partial pressure and content fell as did pH whereas CO2 pressures rose during diving. Oxygen consumption at rest was 124 and 102% of that predicted on the basis of body mass for the beaver and nutria, respectively. Rate of decline of O2 stores during diving decreased by 93% in beavers and 89% in nutria compared to the predive value. Regional blood flow decreased to all organs except the adrenals, heart, and lungs. Blood flow to the brain increased during diving.

Adaptation, Physiological↗

Aerobic dive limit: how often does it occur in nature?

Diving animals offer a unique opportunity to study the importance of physiological constraint in their everyday behaviors. An important component of the physiological capability of any diving animal is its aerobic dive limit (ADL). The ADL has only been measured in a few species. The goal of this study was to estimate the aerobic dive limit from measurements of body oxygen stores and at sea metabolism. This calculated ADL (cADL) was then compared to measurements of diving behavior of individual animals of three species of otariids, the Antarctic fur seal, Arctocephalus gazella, the Australian sea lion, Neophoca cinerea, and the New Zealand sea lion, Phocarctos hookeri. Antarctic fur seals dove well within the cADL. In contrast, many individuals of both sea lion species exceeded the cADL, some by significant amounts. Australian sea lions typically dove 1.4 times longer than the cADL, while New Zealand sea lions on average dove 1.5 times longer than the cADL. The tendency to exceed the cADL was correlated with the dive pattern of individual animals. In both Antarctic Fur Seals and Australian sea lions, deeper diving females made longer dives that approached or exceeded the cADL (P<0.01, r(2)=0.54). Australian and New Zealand sea lions with longer bottom times also exceeded the cADL to a greater degree. The two sea lions forage on the benthos while the fur seals feed shallow in the water column. It appears that benthic foraging requires these animals to reach or exceed their aerobic dive limit.

Animals↗

The evolution of a physiological system: the pulmonary surfactant system in diving mammals.

Pulmonary surfactant lines the alveolar air-water interface, varying surface tension with lung volume to increase compliance and prevent adhesion of respiratory surfaces. We examined whether the surfactant system of diving mammals exhibits adaptations for more efficient lung function during diving, to complement other respiratory adaptations. Here we review adaptations at the molecular, compositional, functional and cellular levels and during development for animals beginning life on land and progressing to an aquatic environment. Molecular adaptations to diving were examined in surfactant protein C (SP-C) from terrestrial, semi-aquatic and diving mammals using phylogenetic analyses. Diving species exhibited sites under positive selection in the polar N-terminal domain. These amino acid substitutions may lead to stronger binding of SP-C to the phospholipid film and increased adsorption to the air-liquid interface. The concentration of shorter chain phospholipid molecular species was greater and SP-B levels were lower in diving than terrestrial mammals. This may lead to a greater fluidity and explain the relatively poor surface activity of diving mammal surfactant. There were no consistent differences in cholesterol between diving and terrestrial mammals. Surfactant from newborn California sea lions was similar to that of terrestrial mammals. Secretory activity of alveolar type II epithelial cells of sea lions demonstrated an insensitivity to pressure relative to sheep cells. The poor surface activity of diving mammal surfactant is consistent with the hypothesis that it has an anti-adhesive function that develops after the first entry into the water, with a surfactant film that is better suited to repeated collapse and respreading.

Adaptation, Physiological↗

Diving and pregnancy.

Scuba diving during pregnancy has increased in incidence as a result of substantial growth in the number of young females attracted to sport diving. This review summarizes the physiological changes induced by immersion, diving and decompression, on male and female divers. Furthermore, it extends to literature review, in animal models, of the susceptibility of a pregnant animal to diving decompression injury. Publications regarding reports of diving injury in pregnant humans are also reviewed, comprising very recent material from the sport diving community. It is concluded that there is no countraindication to diving for the normal, healthy, nonpregnant female. However, pregnant females should refrain from diving, because the fetus is not protected from decompression problems and is at risk of malformation and gas embolism after decompression disease. It is prudent to advise pregnant patients of the increased risk of diving problems for the fetus during pregnancy. However, should a woman have completed a dive during early pregnancy because she was unaware she was pregnant, the present evidence is not to recommend an abortion, because several normal pregnancies have been documented even if diving is continued. Snorkeling can still be practiced during pregnancy, but scuba diving should be discontinued until after the birth period.

Animals↗

To what extent is the foraging behaviour of aquatic birds constrained by their physiology?

Aquatic birds have access to limited amounts of usable oxygen when they forage (dive) underwater, so the major physiological constraint to their behaviour is the need to periodically visit the water surface to replenish these stores and remove accumulated carbon dioxide. The size of the oxygen stores and the rate at which they are used (V dot o2) or carbon dioxide accumulates are the ultimate determinants of the duration that aquatic birds can remain feeding underwater. However, the assumption that the decision to terminate a dive is governed solely by the level of the respiratory stores is not always valid. Quantification of an optimal diving model for tufted ducks (Aythya fuligula) shows that while they dive efficiently by spending a minimum amount of time on the surface to replenish the oxygen used during a dive, they dive with nearly full oxygen stores and surface well before these stores are exhausted. The rates of carbon dioxide production during dives and removal during surface intervals are likely to be at least as important a constraint as oxygen; thus, further developments of optimal diving models should account for their effects. In the field, diving birds will adapt to changing environmental conditions and often maximise the time spent submerged during diving bouts. However, other factors influence the diving depths and durations of aquatic birds, and in some circumstances they are unable to forage sufficiently well to provide food for their offspring. The latest developments in telemetry have demonstrated how diving birds can make physiological decisions based on complex environmental factors. Diving penguins can control their inhaled air volume to match the expected depth, likely prey encounter rate, and buoyancy challenges of the following dive.

Animals↗

Otologic and otoneurologic injuries in divers: clinical studies on nine commercial and two sport divers.

In the past two decades, we have seen a great increase in the number of injuries from commercial and sport diving. During this time, our knowledge of the physiology and pathophysiology of diving has also increased. As a result, we now can accurately diagnose and successfully treat many of these injuries. Of the commercial and sport divers examined as pateints in the Department of Otolaryngology at the University of Texas Medical Branch in Galveston, Tex., between September, 1974, and May, 1975, 11 showed positive otologic and otoneurologic findings which are reported herein. One patient was surgically explored for an oval window fistula. In localizing and classifying these injuries, we have utilized extensive and broad-based test batteries, which include complete history, otologic and otoneurologic physical examination, audiometry, a central auditory test battery, and a vestibular test battery. These tests are described. The findings in each of the divers are illustrated and analyzed. This article further describes the use of these test batteries, which were employed to localize otoneurologic pathology in this sample of injured divers. Based on these cases, we have expanded and modified Edmonds' classification of the etiology of vertigo related to diving. We feel that the test batteries which we describe, or similar tests, should be part of the otologic and otoneurologic workup of injuries divers.

Adult↗

Behavior of freely diving animals.

While diving animals are capable of both long-duration and deep dives, their normal behavior does not routinely approach these limits of time and depth. Studies of the physiologic and biochemical capabilities of diving species have defined the maximum limits of their underwater periods. However, by also studying their diving behavior, we can examine how diving animals most efficiently work within those limits. If we assume for example that the behavioral goal of a foraging seal is to spend as much time underwater as possible, then it must also minimize time at the surface and make many repetitive dives instead of single, longer dives that require long surface recovery periods. To understand the efficiency of bout diving, we must study the physiologic impact of many repetitive dives and how the seal manipulates its behavior to both stay within its physiologic limits and to maximize time underwater.

Animals↗