Thermal Significance of the Topographical Distribution of Blubber in Ringed Seals (Phoca hispida)

1988 ◽  
Vol 45 (6) ◽  
pp. 985-992 ◽  
Author(s):  
Morten Ryg ◽  
Thomas G. Smith ◽  
Nils Are Øritsland
Keyword(s):  
Surface Area ◽  
Heat Loss ◽  
Thermal Effects ◽  
Marine Mammals ◽  
The Body ◽  
Phoca Hispida ◽  
Ringed Seals ◽  
Linear Dimensions ◽  
Topographical Distribution ◽  
Body Core

The distribution of blubber in ringed seals (Phoca hispida) and relationships between surface area, body mass, and linear dimensions are described. The blubber was distributed in such a way that the ratio of blubber thickness to body radius is nearly constant over the body, maximizing the available blubber for insulation. The hind part of the body has a higher thickness to radius ratio and is thus "overinsulated." During periods of mass loss, fat is lost fastest from this overinsulated region, thus reducing the negative thermal effects of the fat loss. We present formulae for calculating body surface area and an effective, or "equivalent blubber thickness," for calculations of heat loss and suggest that these formulae are independent of size and shape. By combining these equations, we arrive at a general formula for calculating a lower limit for heat loss from marine mammals. According to this formula, thermal stability can be maintained when blubber is lost if mass is simultaneously lost from the body core.

Restoration of thermoregulation after exercise

2017 ◽  
Vol 122 (4) ◽  
pp. 933-944 ◽  
Author(s):  
Glen P. Kenny ◽  
Ryan McGinn
Keyword(s):  
Heat Loss ◽  
Core Temperature ◽  
Current Knowledge ◽  
Thermal Control ◽  
The Body ◽  
Body Core Temperature ◽  
Whole Body ◽  
Temperature Sensitive ◽  
Internal Core ◽  
Body Core

Performing exercise, especially in hot conditions, can heat the body, causing significant increases in internal body temperature. To offset this increase, powerful and highly developed autonomic thermoregulatory responses (i.e., skin blood flow and sweating) are activated to enhance whole body heat loss; a response mediated by temperature-sensitive receptors in both the skin and the internal core regions of the body. Independent of thermal control of heat loss, nonthermal factors can have profound consequences on the body’s ability to dissipate heat during exercise. These include the activation of the body’s sensory receptors (i.e., baroreceptors, metaboreceptors, mechanoreceptors, etc.) as well as phenotypic factors such as age, sex, acclimation, fitness, and chronic diseases (e.g., diabetes). The influence of these factors extends into recovery such that marked impairments in thermoregulatory function occur, leading to prolonged and sustained elevations in body core temperature. Irrespective of the level of hyperthermia, there is a time-dependent suppression of the body’s physiological ability to dissipate heat. This delay in the restoration of postexercise thermoregulation has been associated with disturbances in cardiovascular function which manifest most commonly as postexercise hypotension. This review examines the current knowledge regarding the restoration of thermoregulation postexercise. In addition, the factors that are thought to accelerate or delay the return of body core temperature to resting levels are highlighted with a particular emphasis on strategies to manage heat stress in athletic and/or occupational settings.

Thermal effects of dorsal head immersion in cold water on nonshivering humans

2005 ◽  
Vol 99 (5) ◽  
pp. 1958-1964 ◽  
Author(s):  
Gordon G. Giesbrecht ◽  
Tamara L. Lockhart ◽  
Gerald K. Bristow ◽  
Allan M. Steinman
Keyword(s):  
Heat Loss ◽  
Heat Production ◽  
Thermal Effects ◽  
Cold Water ◽  
The Body ◽  
Whole Body ◽  
Esophageal Temperature ◽  
Confounding Effect ◽  
Core Cooling ◽  
Stimulation Of

Personal floatation devices maintain either a semirecumbent flotation posture with the head and upper chest out of the water or a horizontal flotation posture with the dorsal head and whole body immersed. The contribution of dorsal head and upper chest immersion to core cooling in cold water was isolated when the confounding effect of shivering heat production was inhibited with meperidine (Demerol, 2.5 mg/kg). Six male volunteers were immersed four times for up to 60 min, or until esophageal temperature = 34°C. An insulated hoodless dry suit or two different personal floatation devices were used to create four conditions: 1) body insulated, head out; 2) body insulated, dorsal head immersed; 3) body exposed, head (and upper chest) out; and 4) body exposed, dorsal head (and upper chest) immersed. When the body was insulated, dorsal head immersion did not affect core cooling rate (1.1°C/h) compared with head-out conditions (0.7°C/h). When the body was exposed, however, the rate of core cooling increased by 40% from 3.6°C/h with the head out to 5.0°C/h with the dorsal head and upper chest immersed ( P < 0.01). Heat loss from the dorsal head and upper chest was approximately proportional to the extra surface area that was immersed (∼10%). The exaggerated core cooling during dorsal head immersion (40% increase) may result from the extra heat loss affecting a smaller thermal core due to intense thermal stimulation of the body and head and resultant peripheral vasoconstriction. Dorsal head and upper chest immersion in cold water increases the rate of core cooling and decreases potential survival time.

Control of respiratory evaporative heat loss in exercising goats

1979 ◽  
Vol 46 (5) ◽  
pp. 978-983 ◽  
Author(s):  
J. B. Mercer ◽  
C. Jessen
Keyword(s):  
Heat Loss ◽  
Core Temperature ◽  
Heat Exchangers ◽  
The Body ◽  
Body Core Temperature ◽  
Evaporative Heat Loss ◽  
Hypothalamic Temperature ◽  
Body Core ◽  
Total Body ◽  
Rest And Exercise

Investigations were carried out to determine whether a nonthermal input is involved in the control of respiratory evaporative heat loss (REHL) in exercising goats. Two goats were implanted with hypothalamic perfusion thermodes and three goats were implanted with intravascular heat exchangers to clamp hypothalamic temperature and total body core temperature, respectively. At 30 degrees C air temperature REHL was measured while the animals were resting or walking on a treadmill (3 km.h-1, 5 degrees gradient). When the hypothalamic temperature was clamped between 33.0 and 43.0 degrees C the slopes of the responses relating increased REHL to hypothalamic temperature were similar during rest and exercise. However, the threshold hypothalamic temperatures for the increased REHL responses were lower during exercise than at rest, presumably due to higher extrahypothalamic temperatures. When the body core temperature was clamped between 37.0 and 40.4 degrees C the slopes of the responses relating increased REHL to total body core temperature during exercise showed only minor differences compared to those at rest, none of them conclusively indicating nonthermal influences.

Assessment of claw growth-layer groups from ringed seals (Pusa hispida) as biomonitors of inter- and intra-annual Hg, δ15N, and δ13C variation

2011 ◽  
Vol 89 (9) ◽  
pp. 774-784 ◽  
Author(s):  
Elizabeth O. Ferreira ◽  
Lisa L. Loseto ◽  
Steven H. Ferguson
Keyword(s):  
Life History ◽  
Marine Mammals ◽  
Ringed Seal ◽  
The Body ◽  
Conservation Strategies ◽  
Growth Layer ◽  
Annual Variations ◽  
Ringed Seals ◽  
Pusa Hispida ◽  
Layer Groups

The ringed seal ( Pusa hispida (Schreber, 1775)) is a sentinel species of arctic marine mammals; therefore, methods to monitor its life-history changes are crucial to establish effective conservation strategies. We evaluate the potential use of claws of ringed seals as a proxy for counts of tooth growth-layer groups (age) and a biomonitor of total mercury burden (THg) and diet (stable isotope ratios expressed as δ15N and δ13C). The count of claw growth-layer groups was indicative of age up to 8 years and we infer differentiation of dark and light annuli as being associated with the spring moult. No differences of THg, δ15N, or δ13C were observed among flipper digits. The proximal claw annulus representing the most recent growth had δ13C values that were correlated to both muscle and liver δ13C, supporting the use of claws to monitor visceral δ13C. Claw log10THg from the proximate annulus was significantly correlated to liver and whisker log10THg, while significant interannual THg accumulation was observed in 18 of 32 seals ≥4 years, suggesting the claws receive and disperse Hg from active tissues of the body. Results support the use of claw tissue from ringed seal to provide a chronological record of inter- and intra-annual variations representing seal diet, contaminant load, and life history.

Thermal effects of whole head submersion in cold water on nonshivering humans

2006 ◽  
Vol 101 (2) ◽  
pp. 669-675 ◽  
Author(s):  
Thea Pretorius ◽  
Gerald K. Bristow ◽  
Alan M. Steinman ◽  
Gordon G. Giesbrecht
Keyword(s):  
Heat Loss ◽  
Body Mass ◽  
Cold Water ◽  
Surface Heat ◽  
The Body ◽  
Total Heat ◽  
Total Heat Loss ◽  
Body Core ◽  
Core Cooling ◽  
Male Subjects

This study isolated the effect of whole head submersion in cold water, on surface heat loss and body core cooling, when the confounding effect of shivering heat production was pharmacologically eliminated. Eight healthy male subjects were studied in 17°C water under four conditions: the body was either insulated or uninsulated, with the head either above the water or completely submersed in each body-insulation subcondition. Shivering was abolished with buspirone (30 mg) and meperidine (2.5 mg/kg), and subjects breathed compressed air throughout all trials. Over the first 30 min of immersion, exposure of the head increased core cooling both in the body-insulated conditions (head out: 0.47 ± 0.2°C, head in: 0.77 ± 0.2°C; P < 0.05) and the body-exposed conditions (head out: 0.84 ± 0.2°C and head in: 1.17 ± 0.5°C; P < 0.02). Submersion of the head (7% of the body surface area) in the body-exposed conditions increased total heat loss by only 10%. In both body-exposed and body-insulated conditions, head submersion increased core cooling rate much more (average of 42%) than it increased total heat loss. This may be explained by a redistribution of blood flow in response to stimulation of thermosensitive and/or trigeminal receptors in the scalp, neck and face, where a given amount of heat loss would have a greater cooling effect on a smaller perfused body mass. In 17°C water, the head does not contribute relatively more than the rest of the body to surface heat loss; however, a cold-induced reduction of perfused body mass may allow this small increase in heat loss to cause a relatively larger cooling of the body core.

The use of Body Surface Index as a Better Clinical Health indicators Compare to Body Mass Index and Body Surface Area for Clinical Application

2018 ◽  
pp. 131-136
Author(s):  
Shirazu I. ◽  
Theophilus. A. Sackey ◽  
Elvis K. Tiburu ◽  
Mensah Y. B. ◽  
Forson A.
Keyword(s):  
Surface Area ◽  
Body Surface Area ◽  
Clinical Application ◽  
Body Surface ◽  
Body Height ◽  
Health Indicators ◽  
The Body ◽  
Body Parameters ◽  
The Relationship ◽  
Individual Body

The relationship between body height and body weight has been described by using various terms. Notable among them is the body mass index, body surface area, body shape index and body surface index. In clinical setting the first descriptive parameter is the BMI scale, which provides information about whether an individual body weight is proportionate to the body height. Since the development of BMI, two other body parameters have been developed in an attempt to determine the relationship between body height and weight. These are the body surface area (BSA) and body surface index (BSI). Generally, these body parameters are described as clinical health indicators that described how healthy an individual body response to the other internal organs. The aim of the study is to discuss the use of BSI as a better clinical health indicator for preclinical assessment of body-organ/tissue relationship. Hence organ health condition as against other body composition. In addition the study is `also to determine the best body parameter the best predict other parameters for clinical application. The model parameters are presented as; modeled height and weight; modelled BSI and BSA, BSI and BMI and modeled BSA and BMI. The models are presented as clinical application software for comfortable working process and designed as GUI and CAD for use in clinical application.

Haul-out behaviour and densities of ringed seals (Phoca hispida) in the Barrow Strait area, N.W.T.

1979 ◽  
Vol 57 (10) ◽  
pp. 1985-1997 ◽  
Author(s):  
Kerwin J. Finley
Keyword(s):  
Wind Speed ◽  
Early Morning ◽  
Maximum Density ◽  
Stable Population ◽  
The Sun ◽  
High Wind ◽  
Phoca Hispida ◽  
High Wind Speed ◽  
Ringed Seals ◽  
Calm Weather

Numbers of ringed seals hauled out on the ice began to increase in early June. Numbers on the ice were highest from 0900 to 1500 hours Central Standard Time and lowest (average 40–50% of peak) in early morning. Seals commonly remained on the ice for several hours, and occasionally (during calm weather) for > 48 h. Numbers on the ice were reduced on windy days and possibly also on unusually warm, bright and calm days. Seals tended to face away from the wind (particularly with high wind speed) and oriented broadside to the sun. Seals usually occurred singly (60–70% of all groups) at their holes.Numbers of seals hauled out at Freemans Cove remained relatively constant during June (maximum density 4.86/km2), whereas at Aston Bay numbers increased dramatically to a maximum density of 10.44/km2 in late June. The increase was thought to be due to an influx of seals abandoning unstable ice. The density of seal holes at Freemans Cove (5.92/km2) was much higher than at Aston Bay (2.73/km2). The ratio of holes to the maximum numbers of seals (1.12:1) at Freemans Cove represents a first estimate of this relationship in an apparently stable population.

Distribution and abundance of ringed (Phoca hispida) and bearded seals (Erignathus barbatus) in western Hudson Bay

1997 ◽  
Vol 54 (4) ◽  
pp. 914-921 ◽  
Author(s):  
N J Lunn ◽  
I Stirling ◽  
S N Nowicki
Keyword(s):  
Polar Bear ◽  
Hudson Bay ◽  
Phoca Hispida ◽  
Current Estimate ◽  
Ringed Seals ◽  
Erignathus Barbatus ◽  
The Mean ◽  
Western Hudson Bay ◽  
The Relationship ◽  
Bearded Seals

We flew a medium-altitude, systematic, strip-transect survey for ringed (Phoca hispida) and bearded seals (Erignathus barbatus) over western Hudson Bay in early June 1994 and 1995. The mean density (per square kilometre) of ringed seals hauled out on the ice was four times higher in 1995 (1.690) than in 1994 (0.380). The 1994 survey appeared to underestimate seal abundance because it was flown too late. Ringed seals preferred high ice cover habitat (6 + /8 ice) and, within this habitat, favoured cracking ice and large floes. We found no consistent effect of either wind or cloud cover on habitat preference. We estimated a total of 1980 bearded seals and 140<|>880 ringed seals hauled out on the sea ice in June 1995. A recent review of the relationship between ringed seal and polar bear (Ursus maritimus) populations suggests that a visible population of this size should support a population of up to 1300 polar bears, which is in general agreement with the current estimate of 1250-1300 bears in western Hudson Bay.

Metabolic adjustments to breath holding in higher vertebrates

1989 ◽  
Vol 67 (12) ◽  
pp. 3024-3031 ◽  
Author(s):  
P. J. Butler
Keyword(s):  
Marine Mammals ◽  
Lactate Production ◽  
Weddell Seal ◽  
Specific Dynamic Action ◽  
The Body ◽  
Breath Holding ◽  
Reduced Body ◽  
Key Factor ◽  
Reduced Rate ◽  
Anaerobic Production

There is substantial behavioural and physiological evidence to suggest that most feeding dives by aquatic birds and mammals are aerobic in nature, with no net production of lactate. Any increase in lactate production is matched by increased removal. This does not mean, however, that there are no cardiovascular adjustments associated with such dives. Nonactive parts of the body (including the large pectoral muscles in diving ducks) may be hypoperfused and consume oxygen at a reduced rate. For example, in marine mammals, such as the Weddell seal, reduced perfusion of the gut during a feeding period (which can last for up to 12 h) would reduce the energy expenditure associated with the digestion and assimilation of food (specific dynamic action). Reperfusion during the nonfeeding period would contribute to an unusually high "resting" oxygen uptake. Although some tissues in seals at least can tolerate periods of ischaemia, there is no evidence to suggest that enhanced anaerobic production of ATP is a key factor in the survival of marine mammals during unusually long periods underwater. There may, in fact, be an overall reduction in the ATP requirements of certain tissues, possibly as a result of a reduction in the permeability of cell membranes to some ions, but most certainly as a result of reduced body temperature. During relatively long dives, lactate production eventually exceeds its rate of removal and it accumulates. Precisely what occurs in the muscles is not known. One suggestion is that periods of vasoconstriction are interrupted by vasodilatation, when the oxygen stores are replaced.

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