IMPROVED MEASUREMENT OF THE EFFECT OF INTRAVENOUSLY INJECTED ADRENALIN ON THE RESPIRATORY EXCHANGE BY COLORIMETRIC DETERMINATION OF CARBON DIOXIDE IN EXPIRED AIR AND CONTINUOUS GRAPHIC REGISTRATION OF OXYGEN CONSUMPTION

1944 ◽  
Vol 142 (5) ◽  
pp. 744-757 ◽  
Author(s):  
Richard J. Jones ◽  
Fred R. Griffith

There are a variety of ways in which the duration of the recovery period after exercise can be determined. The method most frequently employed depends upon observations of the respiratory metabolism. This method has been chosen because the respiratory changes due to exercise can be followed with reasonable ease and accuracy, and because these changes are among the last of the more obvious effects of the exercise to disappear during recovery. In addition, interesting data concerning the effects of exercise on respiratory metabolism can be collected during the determination of the duration of the recovery period when this method is used. In determining the duration of the recovery period by observation of the respiratory metabolism, it is necessary to decide when the carbon dioxide output and oxygen intake have returned to their normal values and are no longer affected by the process of recovery from the exercise. This decision has been made in a variety of ways by different investigators. Some have made one or more pre-exercise determinations of the subject's basal oxygen intake and carbon dioxide output. Recovery was said to be complete when the carbon dioxide output and oxygen consumption returned to these values after exercise. Others found that the oxygen consumption did not return to the pre-exercise level within a reasonable length of time, but remained above normal for several hours. They considered that recovery was complete when the carbon dioxide output and oxygen intake returned to a steady level after exercise, even if the level was not the same as that before exercise.


2012 ◽  
Vol 9 (7) ◽  
pp. 1009-1011 ◽  
Author(s):  
Christopher Reiff ◽  
Kara Marlatt ◽  
Donald R. Dengel

Background:Traditional desks require students to sit; however, recently schools have provided students with nontraditional standing desks. The purpose of this study was to investigate differences in caloric expenditure of young adults while sitting at a standard classroom desk and standing at a nontraditional standing classroom desk.Methods:Twenty (10 male/10 female) young (22.8 ± 1.9 y), healthy participants reported to the laboratory between the hours of 7:00 AM and 2:00 PM following a 12-h fast and 48-h break in exercise. Participants were randomly assigned to perform a series of mathematical problems either sitting at a normal classroom desk or standing at a nontraditional standing desk. Inspired and expired gases were collected for 45-min for the determination of oxygen consumption (VO2), carbon dioxide production (VCO2), and minute ventilation (VE) using a metabolic gas system.Results:There were significant increases from sitting to standing in VO2 (0.22 ± 0.05 vs. 0.28 ± 0.05 L·min−1, P ≤ .0001), VCO2 (0.18 ± 0.05 vs. 0.24 ± 0.050 L·min−1, P ≤ .0001), VE (7.72 ± 0.67 vs. 9.41 ± 1.20 L·min−1, P ≤ .0001), and kilocalories expended per minute (1.36 ± 0.20 kcal/ min, P ≤ .0001 vs. 1.02 ± 0.22 kcal/min, P ≤ .0001).Conclusions:Results indicate a significant increase in caloric expenditure in subjects that were standing at a standing classroom desk compared with sitting at a standard classroom desk.


1975 ◽  
Vol 67 (2) ◽  
pp. 669-671 ◽  
Author(s):  
Joel Garbus ◽  
Roger M. Miller ◽  
Mary J. Caponite ◽  
Claudia S. Myers

1959 ◽  
Vol 36 (2) ◽  
pp. 193-201 ◽  
Author(s):  
Julius A. Goldbarg ◽  
Esteban P. Pineda ◽  
Benjamin M. Banks ◽  
Alexander M. Rutenburg

2013 ◽  
Vol 12 (7) ◽  
pp. 460-465
Author(s):  
Sameer Amereih ◽  
Zaher Barghouthi ◽  
Lamees Majjiad

A sensitive colorimetric determination of fluoride in drinking water has been developed using a polymeric zirconium complex of 5-(2-Carboxyphenylazo)-8-Hydroxyquinoline as fluoride reagents. The method allowed a reliable determination of fluoride in range of (0.0-1.5) mg L-1. The molar absorptivity of the complex formation is 7695 ± 27 L mol-1 cm-1 at 460 nm. The sensitivity, detection limit, quantitation limit, and percentage recovery for 1.0 mg L-1 fluoride for the proposed method were found to be 0.353 ± 0.013 μg mL-1, 0.1 mg L-1, 0.3 mg L-1, and 101.7 ± 4.1, respectively.


Author(s):  
Grażyna Mazurkiewicz-Boroń ◽  
Teresa Bednarz ◽  
Elżbieta Wilk-Woźniak

Microbial efficiency in a meromictic reservoirIndices of microbial efficiency (expressed as oxygen consumption and carbon dioxide release) were determined in the water column of the meromictic Piaseczno Reservoir (in an opencast sulphur mine), which is rich in sulphur compounds. Phytoplankton abundances were low in both the mixolimnion (up to 15 m depth) and monimolimnion (below 15 m depth). In summer and winter, carbon dioxide release was 3-fold and 5-fold higher, respectively, in the monimolimnion than in the mixolimnion. Laboratory enrichments of the sulphur substrate of the water resulted in a decrease in oxygen consumption rate of by about 42% in mixolimnion samples, and in the carbon dioxide release rate by about 69% in monimolimnion samples. Water temperature, pH and bivalent ion contents were of major importance in shaping the microbial metabolic efficiency in the mixolimnion, whilst in the monimolimnion these relationships were not evident.


Author(s):  
Abbas Shebeeb Al-kadumi ◽  
Sahar Rihan Fadhel ◽  
Mohammed Abdullah Ahmed ◽  
Luma Amer Musa

We proposed two simple, rapid, and convenient spectrophotometric methods are described for the determination of Amoxicillin in bulk and its pharmaceutical preparations. They are based on the measurement of the flame atomic emission of potassium ion (in first method) and colorimetric determination of the green colored solution for manganite ion at 610 nm formed after reaction of Amoxicillin with potassium permanganate as oxidant agent (in the second method) in basic medium. The working conditions of the methods were investigated and optimized. Beer's law plot showed a good correlation in the concentration range of 5-45 μg/ml. The detection limits and relative standared deviations were (2.573, 2.814 μg/ml) (2.137, 2.498) for the flame emission photometric method and (1.844, 2.016 μg/ml) (1.645,1.932) for colorimetric methods for capsules and suspensions respectively. The methods were successfully applied to the determination of Amoxicillin in capsules and suspensions, and the obtained results were in good agreement with the label claim. No interference was observed from the commonly encountered additives and expectancies.


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