Pumping Rates, Water Pressures, and Oxygen Use in Eight Species of Marine Bivalve Molluscs from British Columbia

1990 ◽  
Vol 47 (7) ◽  
pp. 1302-1306 ◽  
Author(s):  
F. R. Bernard ◽  
D. J. Noakes

Pumping characteristics and oxygen utilization for Solemya reidi, Yoldia thraciaeformis, Chlamys hastata, Mytilus edulis, Crassostrea gigas, Clinocardium nuttallii, Saxidomus giganteus, and Mya truncata were studied. Pressures were recorded using a Yale A79 spinal tap needle inserted in the pallial cavity or siphonal aperture. Pumping volumes were determined through particulate analysis using a Model B Coulter counter and oxygen consumption by standard Winkler titration modified for small samples. The species chosen were selected to represent progressive increases in gill complexity and siphon length. The minimum pressure differential across the gill (20 Pa) was observed for Y. thraciaeformis while the maximum pressure gradient (600 Pa) was recorded for M. truncata. Pumping rates varied from 1.41 L∙h−1∙g−1 (Y. thraciaeformis) to 4.71 L∙h−1∙g−1 (C. hastata) and species with siphons tended to pump at lower rates. The deeply burrowing M. truncata consumed 3.5 times as much oxygen (0.63 mL O2∙h−1∙g−1) as S. reidi (0.18 mL O2∙h−1∙g−1) which inhabits anoxic environments. For all species, the metabolic cost of pumping was less than 1% of the total oxygen uptake.

1974 ◽  
Vol 60 (1) ◽  
pp. 195-206 ◽  
Author(s):  
B. R. McMAHON ◽  
W. W. BURGGREN ◽  
J. L. WILKENS

1. Changes in the rate and force of scaphognathite beating, irrigation volume, oxygen utilization, oxygen consumption and heart rate during acclimation in response to the experimental conditions and in response to long-term hypoxic exposure have been measured in the crayfish Orconectes virilis. 2. Immediately following placement in the experimental chamber the animals exhibited very high levels of respiratory and circulatory performance. These levels decreased slowly and stable minimal performance levels could be measured only after 2-3 days. A 3-day acclimation period under normoxic conditions thus routinely preceded hypoxic experiments to ensure measurement of unmasked hypoxic responses. 3. Two responses to hypoxia were routinely observed: an initial hyperirrigation response maintained oxygen consumption by increased branchial water flow. This response was not maintained, but oxygen consumption remained at pre-hypoxic levels while pumping rates decreased. 4. Possible mechanisms of acclimation to hypoxia are discussed.


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

1992 ◽  
Vol 162 (2) ◽  
pp. 253-263 ◽  
Author(s):  
Natalia V. Zhukova ◽  
Vladimir I. Kharlamenko ◽  
Vasilii I. Svetashev ◽  
Igor A. Rodionov

1997 ◽  
Vol 48 (8) ◽  
pp. 889 ◽  
Author(s):  
H. Harry Taylor ◽  
Francesca M. Waldron

Air-exposure of settled Jasus edwardsii at 17˚C initially halved oxygen consumption, doubled ventilation frequency and reduced heart rate. During 8 h emersion, oxygen uptake partially recovered, ventilation remained elevated and heart rate was restored. Haemolymph PCO2 increased fourfold, despite the hyperventilation. Branchial gas exchange, initially impaired in air, may improve as the gills drain. Partial anaerobiosis was indicated by elevation of haemolymph [lactate-] to 4.2 mmol L-1. Although haemolymph pH decreased ~0.3 units over 8 h, a base excess compensated all of the metabolic and part of the respiratory acidosis. On return to water, oxygen consumption initially increased to >2.5 times pre-emersion rates while ventilation and heart rates increased further. Most respiratory variables returned to pre-emersion levels within 8 h of re- immersion, but oxygen consumption and heart rate remained elevated for 24 h. The excess oxygen consumption over resting rate during 24 h recovery in water indicated a metabolic cost of 8 h emersion equivalent to 10 h resting metabolism in water. These responses contrast with better acid–base compensation previously reported for undisturbed Homarus gammarus in air and worse tolerance of air-exposure by Panulirus argus


1999 ◽  
Vol 86 (5) ◽  
pp. 1657-1662 ◽  
Author(s):  
Young-Hui Chang ◽  
Rodger Kram

Previous studies have suggested that generating vertical force on the ground to support body weight (BWt) is the major determinant of the metabolic cost of running. Because horizontal forces exerted on the ground are often an order of magnitude smaller than vertical forces, some have reasoned that they have negligible cost. Using applied horizontal forces (AHF; negative is impeding, positive is aiding) equal to −6, −3, 0, +3, +6, +9, +12, and +15% of BWt, we estimated the cost of generating horizontal forces while subjects were running at 3.3 m/s. We measured rates of oxygen consumption (V˙o 2) for eight subjects. We then used a force-measuring treadmill to measure ground reaction forces from another eight subjects. With an AHF of −6% BWt,V˙o 2 increased 30% compared with normal running, presumably because of the extra work involved. With an AHF of +15% BWt, the subjects exerted ∼70% less propulsive impulse and exhibited a 33% reduction inV˙o 2. Our data suggest that generating horizontal propulsive forces constitutes more than one-third of the total metabolic cost of normal running.


2019 ◽  
Vol 143 ◽  
pp. 101-110 ◽  
Author(s):  
Hanna Schade ◽  
Nikolas Arneth ◽  
Martin Powilleit ◽  
Stefan Forster

1987 ◽  
Vol 131 (1) ◽  
pp. 137-157
Author(s):  
D. F. HOULIHAN ◽  
C. AGNISOLA ◽  
N. M. HAMILTON ◽  
I. TRARA GENOINO

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.


2005 ◽  
Vol 288 (4) ◽  
pp. H1515-H1520 ◽  
Author(s):  
Nanae Hangai-Hoger ◽  
Amy G. Tsai ◽  
Barbara Friesenecker ◽  
Pedro Cabrales ◽  
Marcos Intaglietta

The microvascular distribution of oxygen was studied in the arterioles and venules of the awake hamster window chamber preparation to determine the contribution of vascular smooth muscle relaxation to oxygen consumption of the microvascular wall during verapamil-induced vasodilatation. Verapamil HCl delivered in a 0.1 mg/kg bolus injection followed by a continuous infusion of 0.01 mg·kg−1·min−1 caused significant arteriolar dilatation, increased microvascular flow and functional capillary density, and decreased arteriolar vessel wall transmural Po2 difference. Verapamil caused tissue Po2 to increase from 25.5 ± 4.1 mmHg under control condition to 32.0 ± 3.7 mmHg during verapamil treatment. Total oxygen released by the microcirculation to the tissue remained the same as at baseline. Maintenance of the same level of oxygen release to the tissue, increased tissue Po2, and decreased wall oxygen concentration gradient are compatible if vasodilatation significantly lowers vessel wall oxygen consumption, which in this model appears to constitute an important oxygen-consuming compartment. These findings show that treatment with verapamil, which increases oxygen supply through vasodilatation, may further improve tissue oxygenation by lowering oxygen consumption of the microcirculation.


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