Respiration of the amphibious fishes Periophthalmus cantonensis and Boleophthalmus chinensis in water and on land

1976 ◽  
Vol 65 (1) ◽  
pp. 97-107 ◽  
Author(s):  
S. O. Tamura ◽  
H. Morii ◽  
M. Yuzuriha
Keyword(s):  
Oxygen Consumption ◽  
Oxygen Uptake ◽  
Terrestrial Habitat ◽  
Total Oxygen ◽  
Total Uptake ◽  
Amphibious Fishes

1. The routine oxygen consumption by Periophthalmus cantonensis and Boleophthalmus chinensis in water increased geometrically, whereas that in air increased logarithmically with temperature. At temperatures of more than 20 degrees C the oxygen uptake of both species was greater in water than in air. 2. When the fishes were able freely to select either an aquatic or terrestrial habitat, the total oxygen consumption of Periophthalmus and Boleophthalmus was 236 and 110 ml/kg, h at 20 degrees C respectively; 66% (Periophthalmus) and 70% (Boleophthalmus) of the total uptake was from water, and 34 and 30% of the total uptake was from air at 20 +/− 1 degrees C. 3. Oxygen uptake of fish limited to aquatic or terrestial life was less than when they could freely select their habitat; for Periophthalmus, uptake was reduced to 83% when confined in water and to 50% in air, and for Bolephthalmus, to 65% in water and to 43% in air. 4. The proportion of oxygen uptake by the gill in water was 52% for Periophthalmus and 59% for Boleophthalmus; in air the corresponding figures were 27 and 52%. 5. The proportions of oxygen uptake via the skin in water was 48% for Periophthalmus and 36% for Boleophthalmus; in air the corresponding figures were 76 and 43%. 6. It is concluded that, on land, Periophthalmus relies mainly on its skin and Boleophthalmus relies mainly on its gills.

Hourly and total oxygen consumption by ova of Atlantic salmon, Salmo salar L., during embryogenesis, at two temperatures and three levels of dissolved oxygen

1979 ◽  
Vol 57 (6) ◽  
pp. 1196-1200 ◽  
Author(s):  
T. Hamor ◽  
E. T. Garside
Keyword(s):  
Oxygen Consumption ◽  
Atlantic Salmon ◽  
Oxygen Uptake ◽  
Dissolved Oxygen ◽  
Salmo Salar ◽  
Developmental Time ◽  
Total Oxygen ◽  
Weighted Mean ◽  
Atlantic Salmon Salmo Salar ◽  
Two Temperatures

Weighted mean hourly rates of oxygen consumption in embryonated ova of Atlantic salmon, Salmo salar L., during embryogenesis, were reduced significantly by levels of dissolved oxygen below air saturation and by a temperature of 5 °C, relative to those for ova incubated at 10 °C. Total oxygen consumption during embryogenesis also was reduced significantly by the lower levels of dissolved oxygen, but not by temperature. The decrease in the pace of embryogenesis in the lots of ova at 5 °C extended the developmental time so that the lower rate of oxygen uptake was offset. Thus, within each level of dissolved oxygen there was no appreciable difference in the products of time units and units of oxygen uptake. At 5 °C, 100% air saturation, mean hourly uptake was 0.0141 mg O2/ovum, and total uptake was 28.153 mg O2/ovum. At 10 °C, 100% air saturation, these values were 0.0270 mg O2/ovum, and 27.974 mg O2/ovum, respectively. Values for ova incubated at 50 and 30% air saturation were correspondingly lower.

Influence of Endogenous OUR Determination on the KLa$${K_L}a$$, Exogenous OUR, Total Oxygen Consumption and Heterotrophic Yield in a Completely Mixed Batch Reactor

2014 ◽  
Vol 12 (2) ◽  
pp. 695-704 ◽  
Author(s):  
R. Zamouche-Zerdazi ◽  
M. Bencheikh Lehocine ◽  
A.-H. Meniai
Keyword(s):  
Wastewater Treatment ◽  
Oxygen Consumption ◽  
Oxygen Uptake ◽  
Uptake Rate ◽  
Oxygen Uptake Rate ◽  
Batch Reactor ◽  
Total Oxygen ◽  
Biomass Activity ◽  
Biological Reaction ◽  
Global Nature

Abstract In wastewater treatment, waste removal and biomass activity are important processes which need to be monitored for a good process control. The difficulties in the interpretation of the total COD, BOD and VSS measurements encouraged the development of respirometric methods for assessing the kinetic constants. Respirometry is an important technique in assessing biological reaction in wastewater treatment. $${K_L}a$$, depends on endogenous oxygen uptake rate (OURend), is a key constant in evaluating respirogram-specific parameters. Generally, OURend is assumed constant in the dissolved oxygen equations. However, it is not the case. Consequently, this paper deals with the influence of OURend calculations region on $${K_L}a$$ determination, exogenous oxygen uptake rate (OURexo), total oxygen consumption and heterotrophic yield (YH). It was shown that the value of OURend and $${K_L}a$$ varied considerably, a maximum of 56%, depending on where to consider Cfin, on the oxygen concentration variation curve. Even though, the variation on OURend and $${K_L}a$$ is important its influence on Yo/x and YH is attenuated to 7.5% and 6%, respectively. This may be due to the local nature of the first parameters (OURend and $${K_L}a$$) and the global nature of the later ones. Moreover, this can be seen through the variation of the calculated amount of oxygen consumed (QThete) which is of the order 7.6%.

scholarly journals Aerial Versus Aquatic Oxygen Consumption in Larvae of the Clawed Frog, Xenopus Laevis

1984 ◽  
Vol 108 (1) ◽  
pp. 231-245 ◽  
Author(s):  
MARTIN E. FEDER ◽  
RICHARD J. WASSERSUG
Keyword(s):  
Oxygen Consumption ◽  
Oxygen Uptake ◽  
Xenopus Laevis ◽  
Total Oxygen ◽  
Pumping Rate ◽  
Aerial Respiration ◽  
Aquatic Respiration ◽  
Normal Feeding ◽  
Hypoxic Water ◽  
Clawed Frog

Tadpoles of Xenopus laevis Daudin can extract oxygen from both air and water. When these larvae have access to air, aerial oxygen uptake averages 16.6% of total oxygen consumption in normoxic water, and increases to 100% of net oxygen consumption in hypoxic water. Neither anaerobiosis nor increased buccopharyngeal ventilation occur in response to hypoxia. If tadpoles are prevented from surfacing to breathe air, they can maintain normal oxygen consumption through aquatic respiration alone in normoxic water, but not in hypoxic water. Unlike air-breathing larvae, exclusively water-breathing larvae respond to aquatic hypoxia by increasing their buccal pumping rate and by accumulating lactate. Even though Xenopus larvae can survive without air for many days, aerial respiration is necessary for other functions: tolerance of hypoxia, normal feeding, locomotion and buoyancy regulation.

scholarly journals No major thermogenic role for (Na+ + K+)-dependent adenosine triphosphatase apparent in hepatocytes from hyperthyroid rats

1982 ◽  
Vol 202 (3) ◽  
pp. 661-665 ◽  
Author(s):  
D G Clark ◽  
M Brinkman ◽  
O H Filsell ◽  
S J Lewis ◽  
M N Berry
Keyword(s):  
Oxygen Consumption ◽  
Oxygen Uptake ◽  
Atpase Activity ◽  
Heat Production ◽  
Adenosine Triphosphatase ◽  
Heat Output ◽  
Liver Parenchymal ◽  
Dependent Atpase ◽  
Parenchymal Cells ◽  
Isolated Liver

(Na+ + K+)-dependent ATPase activity, heat production and oxygen consumption were increased by 59%, 62% and 75% respectively in hepatocytes from tri-iodothyronine-treated rats. Ouabain at concentrations of 1 and 10 mM decreased oxygen uptake by 2-8% in hepatocytes from euthyroid rats and by 5-15% in hepatocytes from hyperthyroid animals. Heat output was decreased by 4-9% with the glycoside in isolated liver parenchymal cells from the control animals and by 11% in the cells from the tri-iodothyronine-treated animals. These results do not support the hypothesis that hepatic (Na+ + K+)-ATPase plays a major role in increased heat production in hepatocytes from hyperthyroid rats.

Myocardial and Total Oxygen Consumption with Halothane

1967 ◽  
Vol 28 (6) ◽  
pp. 1042-1047 ◽  
Author(s):  
Richard A. Theye
Keyword(s):  
Oxygen Consumption ◽  
Total Oxygen

The effect of the acanthocephalan Pomphorhynchus laevis upon the respiration of its intermediate host, Gammarus pulex

Parasitology ◽  
1974 ◽  
Vol 68 (2) ◽  
pp. 271-284 ◽  
Author(s):  
A. E. Rumpus ◽  
C. R. Kennedy
Keyword(s):  
Oxygen Consumption ◽  
Oxygen Uptake ◽  
Host Population ◽  
Gammarus Pulex ◽  
Multiple Infections ◽  
Pomphorhynchus Laevis ◽  
Respiration Rates ◽  
Physiological Processes ◽  
Stage Of Development ◽  
Host Parasite

The respiration rates of individual Gammarus pulex infected by larval Pomphorhynchus laevis were investigated with particular reference to the stage of development of the host and parasite and to the water temperature. At 20°C the oxygen consumption of Gammarus of all sizes was reduced by an average of 19·3 % by the presence of cystacanths of the parasite, but was unaffected by the presence of acanthellae. It is considered that the small size of this larval stage, in relation to that of its host, is responsible for the failure to detect an effect. Multiple infections did not exert any greater effect upon host respiration than single cystacanths, nor did it appear that the parasite had different effects upon hosts of different sexes. At 10°C no significant differences were observed between the respiration rates of infected and uninfected gammarids. The parasite was probably still depressing the host respiration rate at this temperature, but the oxygen uptake of G. pulex is so low that the differences between infected and uninfected individuals were too small to be detected. The parasite has a direct effect upon the physiological processes of the host, but neither the mechanism of this nor the reasons for the different effects found in different host-parasite systems are yet understood. Despite the pronounced effect of P. laevis on respiration of individual hosts, its effect upon the oxygen consumption of a natural host population is small since only a small proportion of the population carries infections and water temperatures remain below 10°C for over half the year.

Appearance of excess lactate in anesthetized dogs during anemic and hypoxic hypoxia

1965 ◽  
Vol 209 (3) ◽  
pp. 604-610 ◽  
Author(s):  
Stephen M. Cain
Keyword(s):  
Cardiac Output ◽  
Oxygen Uptake ◽  
Oxygen Transport ◽  
Liver Dysfunction ◽  
Hypoxic Hypoxia ◽  
Blood Gas ◽  
Total Oxygen ◽  
Anesthetized Dogs ◽  
Lactate And Pyruvate ◽  
Mixed Venous

Ten anesthetized, splenectomized dogs were made progressively anemic by replacement of blood with warmed dextran to approximate hematocrits of 30, 20, 15, and 10%. A second group of 10 dogs was made progressively hypoxic by having them inspire 11.4, 9.5, 8.0, and 5.9% O2 in N2. Blood gas contents, pH, and gas tensions were measured in arterial and mixed venous bloods. Cardiac output was calculated from the arteriovenous O2 difference and the O2 uptake. Excess lactate was calculated from measured levels of lactate and pyruvate in blood water. Excess lactate appeared at higher mixed venous Po2 in anemic animals than in hypoxic, 40 mm Hg versus 20 mm Hg. When related to total oxygen transport, however, excess lactate appeared at about the same point (12 ml/kg per min) in both groups. Because liver has been shown to reduce its oxygen uptake with any lowering of perfusate oxygen content, it was suggested that the excess lactate measured during both anemic and hypoxic hypoxia in anesthetized dogs is largely the result of liver dysfunction with respect to lactate.

scholarly journals Oxygen uptake during mineralization of photosynthesized carbon from phytoplankton of the Barra Bonita Reservoir: a mesocosm study

2008 ◽  
Vol 68 (1) ◽  
pp. 115-122 ◽  
Author(s):  
MB. Cunha-Santino ◽  
SP. Gouvêa ◽  
I. Bianchini Jr ◽  
AAH. Vieira
Keyword(s):  
Electrical Conductivity ◽  
Oxygen Consumption ◽  
Oxygen Uptake ◽  
Dissolved Oxygen ◽  
Water Samples ◽  
Microbial Respiration ◽  
Co2 Concentration ◽  
Ph Values ◽  
Organic Products ◽  
Aulacoseira Granulata

This study aimed to discuss and describe the oxygen consumption during aerobic mineralization of organic products (cells and excretion products) from five unialgal cultures: Cryptomonas sp., Microcystis aeruginosa, Anabaena spiroides, Thalassiosira sp. and Aulacoseira granulata. These species were isolated from Barra Bonita reservoir (22º 29’ S and 48º 34’ W) and cultivated in the laboratory. From each culture, two decomposition chambers were prepared; each chamber contained about 130 mg.L-1 of carbon from water samples of the reservoir. The chambers were aerated and incubated in the dark at 20.0 ºC. The concentration of dissolved oxygen, pH values and electrical conductivity of the solutions were determined during a period of 10 days. The results indicated increases in oxygen consumption for all the solutions studied and also for electrical conductivity. The pH values presented a decreasing tendency throughout the experiment. Oxygen consumption varied from 43 (Aulacoseira granulata chamber) to 345 mg O2 g-1 C (Anabaena spiroides chamber). Decrease in pH values was probably due to increase in CO2 concentration from microbial respiration. Increase in electrical conductivity might be due to the liberation of ions during decomposition. The results demonstrate the potentiality of the studied genera in influencing oxygen availability followed by a die-off event. It also indicates the possibility of changing of the electrical conductivity and pH values in the water column due the aerobic algae mineralization.

scholarly journals Oxygen Consumption of the Isolated Heart of Octopus: Effects of Power Output and Hypoxia

1987 ◽  
Vol 131 (1) ◽  
pp. 137-157
Author(s):  
D. F. HOULIHAN ◽  
C. AGNISOLA ◽  
N. M. HAMILTON ◽  
I. TRARA GENOINO
Keyword(s):  
Oxygen Consumption ◽  
Output Power ◽  
Power Output ◽  
Isolated Heart ◽  
Back Pressure ◽  
Octopus Vulgaris ◽  
Total Oxygen ◽  
Coronary Veins ◽  
Output Flow

A technique is described which allowed the measurement of the oxygen consumption of the isolated heart of Octopus vulgaris. Contraction of the heart resulted in an aortic output and a flow through the heart muscle into coronary veins (the coronary output). The flow and oxygen content of the aortic output and the coronary output were measured with variable input pressures and constant output back pressure (volume loaded), variable output back pressure and constant aortic output (pressure loaded), and during hypoxia. Volume loading of the heart resulted in an increase in aortic output, power output and total oxygen consumption. Pressure loading increased power output and total oxygen consumption of the heart. Exposure to hypoxia decreased the aortic output, power output and total cardiac oxygen consumption. In the response of the heart to reduced work, brought about either by a reduced input pressure or by hypoxic perfusate, the power output was linearly related to the total oxygen consumption of the heart. The oxygen extracted from the coronary output accounted for 80–100% of the total oxygen consumption of the heart. Coronary output amounted to 30% of the total cardiac output at maximum power output. In volume-loaded hearts the volume of the coronary output increased as aortic output increased; in pressure-loaded hearts coronary output increased as power output increased, but aortic output remained constant. In hypoxia, the coronary output increased as the aortic output fell. At a perfusate Po2 of around 50 Torr (1 Torr = 133 Pa), the aortic output ceased although the heart continued to beat and the coronary output continued, accounting for all of the oxygen consumption of the heart. The coronary output flow in vitro therefore has the capacity to be varied independently of the aortic output flow to maintain the oxygen supply to the perfused cardiac muscle.

scholarly journals The Circulatory Response to Acute Hypoxia in Octopus

1983 ◽  
Vol 104 (1) ◽  
pp. 59-71 ◽  
Author(s):  
M.J. WELLS ◽  
J. WELLS
Keyword(s):  
Oxygen Uptake ◽  
Acute Hypoxia ◽  
Oxygen Affinity ◽  
Octopus Vulgaris ◽  
Blood Oxygen ◽  
Total Oxygen ◽  
Circulatory Response ◽  
The Central Nervous System ◽  
Blood Oxygen Affinity ◽  
Cutaneous Respiration

Octopus vulgaris can regulate its oxygen uptake in a closed respirometer down to a Poo2 of less than 70 mmHg. As the tankwater Poo2 falls the hearts slow down. Pulse amplitudes and mean pressures fall in the afferent branchial vessels and in the dorsal aorta. Despite behavioural changes - expansion of the interbrachial web and extension of the arms - that might imply this, the proportion of the total oxygen uptake attributable to cutaneous respiration (less than 13%) does not alter as the external Poo2 falls. The response of the hearts to a low Poo2 is not affected by severing the nerve supply from the central nervous system, or by removal of the heart ganglia. It is evidently determined by oxygen lack and not by the accumulation of CO2 or other metabolites, since the same effects are achieved by placing the animals in water where the Poo2 has been reduced by boiling. The conclusion that regulation does not depend upon circulatory responses to hypoxia is considered in the light of recent work on the changes in blood oxygen affinity associated with acute hypoxia in cephalopods.

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