The Swimming of Nymphon Gracile (Pycnogonida): The Energetics of Swimming at Constant Depth

1977 ◽  
Vol 71 (1) ◽  
pp. 205-211
Author(s):  
ELFED MORGAN
Keyword(s):  
Oxygen Consumption ◽  
Metabolic Rate ◽  
Tidal Cycle ◽  
Active Phase ◽  
Constant Depth ◽  
Total Carbohydrate ◽  
Drag Forces ◽  
Rate Of Oxygen Consumption ◽  
The Mean ◽  
Tide Period

1. The mechanical power required by Nymphon for swimming at constant depth has been calculated from drag forces acting on the legs. For an adult male this was found to be 3.4 W kg. Only about 60% of this is used to support the animal's weight in water. 2. The metabolic rate fluctuates spontaneously over a tidal cycle, being greatest during the ebb-tide period. The mean rate of oxygen consumption during the animals least active phase was found to be about 0.1 μlO2 mg−1 h−1. 3. The total carbohydrate and lipid immediately available for combustion have been estimated at 4.64 and 16 μg/mg wet wt respectively. These quantities should be adequate for about 42 h periodic swimming in an adult Nymphon.

Hibernation in the Eastern Pygmy Possum, Cercartetus-Nanus (Marsupialia, Burramyidae)

1993 ◽  
Vol 41 (1) ◽  
pp. 67 ◽  
Author(s):  
F Geiser
Keyword(s):  
Oxygen Consumption ◽  
Body Temperature ◽  
Metabolic Rate ◽  
Air Temperature ◽  
The Body ◽  
Daily Torpor ◽  
Rate Of Oxygen Consumption ◽  
The Mean ◽  
Cercartetus Nanus ◽  
Torpor Bouts

The pattern of torpor was examined in the eastern pygmy possum, Cercartetus nanus (21 g). Animals displayed torpor regularly in the laboratory, and the occurrence of torpor increased with decreasing air temperature (T(a)). At high T(a) (18-degrees-C) animals usually exhibited daily torpor, but torpor bouts of up to 2 days were observed occasionally. The duration of torpor bouts lengthened with a lowering of T(a) and the mean bout duration at T(a) = 5-degrees-C was 17.0 +/- 2.5 days. The minimum metabolic rate (measured as rate of oxygen consumption) of torpid individuals was 0.018 +/- 0.003 mL O2 g-1 h-1, which is less than 2% of the basal metabolic rate. The body temperature (T(b)) Of torpid animals fell to a minimum of 1.3 +/- 0.4-degrees-C. These results clearly demonstrate that Cercartetus nanus is a deep hibernator.

Activity before exercise influences recovery metabolism in the lizard Dipsosaurus dorsalis

2000 ◽  
Vol 203 (12) ◽  
pp. 1809-1815
Author(s):  
D.A. Scholnick ◽  
T.T. Gleeson
Keyword(s):  
Oxygen Consumption ◽  
Metabolic Rate ◽  
Blood Lactate ◽  
Recovery Period ◽  
Maximal Activity ◽  
Warm Up ◽  
Dipsosaurus Dorsalis ◽  
Rate Of Oxygen Consumption ◽  
Lactate Levels ◽  
Blood Lactate Levels

During recovery from even a brief period of exercise, metabolic rate remains elevated above resting levels for extended periods. The intensity and duration of exercise as well as body temperature and hormone levels can influence this excess post-exercise oxygen consumption (EPOC). We examined the influence of activity before exercise (ABE), commonly termed warm-up in endotherms, on EPOC in the desert iguana Dipsosaurus dorsalis. The rate of oxygen consumption and blood lactate levels were measured in 11 female D. dorsalis (mass 41.1 +/− 3.0 g; mean +/− s.e.m.) during rest, after two types of ABE and after 5 min of exhaustive exercise followed by 60 min of recovery. ABE was either single (15 s of maximal activity followed by a 27 min pause) or intermittent (twelve 15 s periods of exercise separated by 2 min pauses). Our results indicate that both single and intermittent ABE reduced recovery metabolic rate. EPOC volumes decreased from 0.261 to 0.156 ml of oxygen consumed during 60 min of recovery when lizards were subjected to intermittent ABE. The average cost of activity (net V(O2) during exercise and 60 min of recovery per distance traveled) was almost 40 % greater in lizards that exercised without any prior activity than in lizards that underwent ABE. Blood lactate levels and removal rates were greatest in animals that underwent ABE. These findings may be of particular importance for terrestrial ectotherms that typically use burst locomotion and have a small aerobic scope and a long recovery period.

METABOLIC REFERENCE STANDARDS FOR THE NEONATE

PEDIATRICS ◽  
1967 ◽  
Vol 39 (5) ◽  
pp. 724-732
Author(s):  
John C. Sinclair ◽  
Jon W. Scopes ◽  
William A. Silverman
Keyword(s):  
Body Composition ◽  
Body Weight ◽  
Oxygen Consumption ◽  
Metabolic Rate ◽  
Extracellular Fluid ◽  
Mean Value ◽  
Reference Standards ◽  
Contributory Factor ◽  
Tissue Mass ◽  
Rate Of Oxygen Consumption

Oxygen consumption of 92 normally grown newborn babies of birth weight 750 to 3,940 gm has been expressed in terms of various metabolic reference standards in order to identify any systematic variation in expression of metabolic rate that is introduced by these bases of reference in the newborn population. It is postulated that differences in body composition comprise a contributory factor to the variation among newborn babies in rate of oxygen consumption per kilogram body weight. The predictive error from a mean value is increased if surface area, body weight, or fat-free body weight is substituted for body weight as a metabolic reference standard. By taking into account known changes in body composition of the fetus with increasing maturity, a compartment representing the active tissue mass is calculated. This corresponds closely to body weight minus extracellular fluid and includes fat. Rate of oxygen consumption is proportional to the size of this compartment over the range of body weights studied. Implications are discussed as to the metabolic rate of adipose tissue in the newborn and body composition among undergrown babies.

scholarly journals Oxygen Consumption Rate of Polychaeta Nereis sp. Different Sizes and Type of Feed

2019 ◽  
Vol 24 (4) ◽  
pp. 159
Author(s):  
Eko Setio Wibowo ◽  
Endah Sri Palupi ◽  
I G A Ayu Ratna Puspitasari ◽  
Atang Atang
Keyword(s):  
Oxygen Consumption ◽  
Metabolic Rate ◽  
Unsaturated Fatty Acids ◽  
Block Design ◽  
Fish Feed ◽  
Randomized Block Design ◽  
Different Types ◽  
Rate Of Oxygen Consumption ◽  
Biological Aspects

Nereis  sp. contains amino acids and unsaturated fatty acids that can improve the quality of gamete stem cells and the quality of the resulting larvae. Nereis  sp. can increase gamete cell maturation in the parent shrimp up to 70%. This triggers the exploitation these worms excessively in nature since there are no cultivation efforts to meet their needs. This condition encourages research on the biological aspects of Nereis  sp. to complement the information that can support the cultivation of the worms. This research was conducted on Nereis  sp. from the Jeruklegi Cilacap area with different types of feed. This study aims to determine the metabolic rate of the worms Nereis  sp. at different sizes by giving different types of feed. This research use immature Nereis  sp. which was maintained at 15 ppt salinity with three different body weight (0.3-0.6 g; 1.1-1.3 g and 1.8-2.04 g) with three different types of feed (D0 feed, feed flour of Spirulina sp. and ornamental fish feed tetra blitsz). The study was conducted experimentally with a randomized block design (RBD) method with six replications. The results showed the rate of oxygen consumption of Nereis  sp. influenced by the size and type of feed given (P<0.05). Nereis  sp. with size of 0.3-0.6 gr indicates the highest metabolic rate.  Nereis  sp. fed with flour of Spirulina sp. shows the highest metabolic rate.  Appropriate feed to support the growth of Nereis  sp. is D0 and tetra blits (low fiber feed). 

Oxygen sensitivity in the insect Prodenia eridania

1960 ◽  
Vol 198 (2) ◽  
pp. 441-444 ◽  
Author(s):  
Arnold M. Clark ◽  
V. J. Cristofalo
Keyword(s):  
Carbon Monoxide ◽  
Oxygen Consumption ◽  
Metabolic Rate ◽  
Adult Stage ◽  
Oxygen Sensitivity ◽  
Rate Of Oxygen Consumption ◽  
Injurious Effects

Both the larval and pupal stages of prodenia eridania are injured by oxygen at increased pressures. The injury is manifested by a reduction in the rate of oxygen consumption, muscular paralysis and failure to develop to the adult stage. In the pupae these effects appear together as a syndrome. Pupae are much more sensitive than larvae. At least 75 psi of oxygen is necessary for injury to larvae while only 45 psi is required to produce injury in the pupae. Injured pupae respire at a rate 2%–5% of the controls while the injured larvae consume oxygen at 60% of the control rate. In attempts to modify this sensitivity by pretreatment with agents which reduce the metabolic rate, it was found that pupae kept at –10°C for 30 minutes before treatment or kept in carbon monoxide or nitrogen for 30 minutes prior to treatment showed none of the injurious effects of oxygen.

Interaction Between Thyroxine and Dibenzyline on Metabolic Rate

1957 ◽  
Vol 191 (3) ◽  
pp. 573-576 ◽  
Author(s):  
Neena B. Schwartz ◽  
Gerald E. Hammond ◽  
Gerald A. Gronert
Keyword(s):  
Oxygen Consumption ◽  
Synergistic Effect ◽  
Metabolic Rate ◽  
Pressor Effect ◽  
Metabolic Rates ◽  
Thyroid Status ◽  
Experimental Animals ◽  
Rate Of Oxygen Consumption

Doses of Dibenzyline adequate to block the pressor effect of epinephrine were administered to rats with various degrees of chronic hypo- or hyperthyroidism. Rate of oxygen consumption was measured under barbiturate anesthesia. Dibenzyline decreased or did not change hypothyroid metabolic rates, but increased metabolic rates in hyperthyroid rats. The data indicated that Dibenzyline exerts a synergistic effect with thyroxine on metabolism resembling the previously reported synergism between thyroxine and epinephrine. Apparently discrepant findings presented in the literature regarding the interaction of thyroxine and Dibenzyline probably result from differences in the thyroid status of the experimental animals.

The Surface of the Heart Leaks Oxygen

Physiology ◽  
1995 ◽  
Vol 10 (3) ◽  
pp. 129-133 ◽  
Author(s):  
DS Loiselle ◽  
JHGM van Beek ◽  
DA Mawson ◽  
PJ Hunter
Keyword(s):  
Oxygen Consumption ◽  
Metabolic Rate ◽  
Basal Metabolic Rate ◽  
Oxygen Exchange ◽  
Fick Principle ◽  
Rate Of Oxygen Consumption

The rate of oxygen consumption of the heart is classically measured using the Fick principle. Uncritical application of this principle can cause errors of measurement, particularly when estimating cardiac basal metabolic rate. Consideration of these errors leads to a model that supports modern notions of oxygen exchange in perfused tissue.

RESPIRATION OF FISHES WITH SPECIAL EMPHASIS ON STANDARD OXYGEN CONSUMPTION: I. INFLUENCE OF WEIGHT AND TEMPERATURE ON RESPIRATION OF GOLDFISH, CARASSIUS AURATUS L.

1964 ◽  
Vol 42 (2) ◽  
pp. 161-175 ◽  
Author(s):  
F. W. H. Beamish ◽  
P. S. Mookherjii
Keyword(s):  
Oxygen Consumption ◽  
Spontaneous Activity ◽  
Carassius Auratus ◽  
Goldfish Carassius Auratus ◽  
Simultaneous Measurements ◽  
Proportionate Change ◽  
Rate Of Oxygen Consumption ◽  
Standard Rate ◽  
The Mean ◽  
External Stimuli

Standard oxygen consumption of goldfish was estimated in relation to weight and temperature from simultaneous measurements of routine oxygen uptake and spontaneous activity. The relation between weight and standard oxygen consumption was expressed as a logarithmic linear regression. For a given shift in temperature, the proportionate change in standard oxygen consumption appears to be independent of weight. The mean slope of the regressions was found to be 0.850.The standard rate of a 100-g goldfish increased linearly, on a semilogarithmic grid, over the temperature range of 10 to 35 °C. The estimates found in the present study were less than the lowest applicable values that could be found in the literature.The average routine rate of oxygen consumption suggests that goldfish display a considerable amount of spontaneous activity despite the elimination of external stimuli.

scholarly journals Oxygen Consumption During the Metamorphosis of the Parasitic Lamprey, Lampetra Fluviatilis (L.) and Its Non-Parasitic Derivative, Lampetra Planeri (Bloch)

1977 ◽  
Vol 69 (1) ◽  
pp. 187-198
Author(s):  
S. V. LEWIS ◽  
I. C. POTTER
Keyword(s):  
Circadian Rhythm ◽  
Oxygen Consumption ◽  
Metabolic Rate ◽  
Life Cycles ◽  
Lampetra Fluviatilis ◽  
Ventilatory Frequency ◽  
Secondary Sexual Characters ◽  
Lampetra Planeri ◽  
Slow Rise ◽  
The Mean

1. Standard oxygen consumption has been measured during the six stages of metamorphosis in both the anadromous parasitic lamprey, Lampetra fluviatilis, and in its non-parasitic derivative, Lampetra planeri. 1. Standard oxygen consumption has been measured during the six stages of metamorphosis in both the anadromous parasitic lamprey, Lampetra fluviatilis, and in its non-parasitic derivative, Lampetra planeri. 2. At 10 °C, the standard rates in larval L. planeri and L. fluviatilis of metamorphosing size were 20.3 and 29.3 μl g−1 h−1 respectively. 3. After a slow rise in oxygen consumption during the initial stages of metamorphosis, the rates reached 50.5 and 60.4 μl g−1 h−1 at stage of 6 of L. planeri and L. fluviatilis respectively. 4. Following the completion of metamorphosis in L. planeri and the development of secondary sexual characters, the mean rate in males rose to 73.3 μl g−1 h−1 compared with a decline in females to 44.1 μl g−1 h−1. 5. Although no circadian rhythm was detectable in the oxygen consumption of larvae, an elevation in the metabolic rate was present during darkness in L. fluviatilis at the end of metamorphosis. 6. Standard oxygen consumption and ventilatory frequency were influenced greatly by temperature, e.g. values for stage 6 of L. fluviatilis rose from 24.3 μl g−1 h−1 and 33.0 beats min−1 at 5 °C to 103.8 μl g−1 h−1 and 98.2 beats min−1 at 15 °C. 7. The results are discussed in the context of the radical changes taking place during metamorphosis and in terms of the differences between larvae and adult and between the life cycles of parasitic and non-parasitic lampreys.

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