Respirometry

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Respirometry is a general term that encompass a number of powerful techniques for obtaining metabolism of vertebrates, invertebrates, plants, or even tissues, or microorganisms via an indirect measure of heat production (calorimetry).

Contents

1 Whole animal metabolic rates

1.1 Closed respirometry
1.2 Open respirometry

1.2.1 Calculations

1.3 Respirometry equipment

2 References
3 See also
4 External links

Whole animal metabolic rates

The metabolism of an animal is estimated by determining rates of carbon dioxide production (VCO₂) and oxygen consumption (VO₂) of individual animals, either in a closed or an open-circuit respirometry system. Two measures are typically obtained: standard (SMR) or basal metabolic rate (BMR) and maximal rate (VO2max). SMR is measured while the animal is at rest (but not asleep) under specific laboratory (temperature, hydration) and subject-specific conditions (e.g., size (see allometry), age, reproduction status, post-absorptive to avoid thermic effect of food). VO₂max is typically determined during aerobic exercise at or near physiological limits. In contrast, field metabolic rate (FMR) refers to the metabolic rate of an unrestrained, active animal in nature.

Whole animal metabolic rates refer to these measures without correction for body mass. If SMR or BMR values are divided by the body mass value for the animal, then the rate is termed mass-specific. It is this mass-specific value that one typically hears in comparisons among species.

Closed respirometry

Respirometry depends on the "what goes in must come out" principle. Consider a closed system first. Imagine that we place a toad into an airtight container. The air sealed in the container initially contains the same composition and proportions of gases that were present in the room: 20.95% O₂, 0.3% CO₂, water vapor (the exact amount depends on air temperature, see dew point), 71% (approximately) N₂, and a variety of trace gases making up the rest (see Earth%27s atmosphere). As time passes, the toad in the chamber produces CO₂ and water vapor, but extracts O₂ from the air in proportion to its metabolic demands. Therefore, as long as we know the volume of the system, the difference between the concentrations of O₂ and CO₂ at the start when we sealed the toad into the chamber (the baseline or reference conditions) compared to the amounts present after the toad has breathed the air at a later time must be the amounts of CO₂/O₂ produced/consumed by the toad. In a closed system, the toad will eventually become hypoxic.

Open respirometry

For an open-system, the situation is a bit more complicated, but the principle remains the same. What goes in must come out. The primary distinction between an open and closed system is that the open system flows air through the chamber (i.e., air is pushed or pulled by pump) at a rate that constantly replenishes the O₂ depleted by the animal while removing the CO₂ and water vapor produced by the animal. The flow rate must be high enough to ensure that the animal never consumes all of the oxygen present in the chamber while at the same time, the rate must be low enough so that the animal consumes enough O₂ for detection. For a 100 g toad, flow rates of about 200 ml/min through 450-900 ml containers would provide a good balance. At this flow rate, about 40 ml of O₂ is brought to the chamber and the entire volume of air in the chamber is exchanged within 5 minutes. For other smaller animals, chamber volumes need to be much smaller and flow rates should be adjusted as well. Note that for warm-blooded or endothermic animals (birds and mammals), chamber sizes and or flow rates should be increased to accommodate their higher metabolic rates.

Calculations

To calculate metabolic rate from rates of oxygen consumed, one needs to know the location of the flow meter relative to the animal chamber (if positioned before the chamber, the flow meter is "upstream," if positioned after the chamber, the flow meter is "downstream"), and whether or not reactive gases are present (e.g., CO₂, water, methane, see inert gas).

For an open system with upstream flow meter, water (e.g., silical gel) and CO₂ (e.g., Ascarite II) removed prior to oxygen analyzer, a suitable equation is

[VO_2 = \frac ]

For an open system with downstream flow meter, water (e.g., silical gel) and CO₂ (e.g., Ascarite II) removed prior to oxygen analyzer, a suitable equation is

[VO_2 = \frac ]

where

FR is the flow rate adjusted to STP (see Standard conditions for temperature and pressure)
FiO₂ is the fractional amount of oxygen present in the incurrent air stream (the baseline or reference), and
FeO₂ is the fractional amount of oxygen present in the excurrent air stream (what the animal has consumed relative to baseline per unit time).

For example, values for BMR of a 20 g mouse (Mus musculus) might be FR = 200 ml/min, and readings of fractional concentration of O₂ from an oxygen analyzer are FiO₂ = 0.2095, FiO₂ = 0.2072. The calculated rate of oxygen consumption is 0.58 ml/min or 35 ml/hour. Assuming an enthalpy of combustion for O₂ of 20.1 Joules/milliliter, we would then calculate the heat production (and therefore metabolism) for the mouse as 703.5 J/hour.

Respirometry equipment

For open flow system, the list of equipment and parts is long compared to the components of a closed system, but the chief advantage of the open system is that it permits continuous recording of metabolic rate. The risk of hypoxia is also much less in an open system.

Pumps for air flow

Vaccuum Pump: a pump is needed to push (i.e., upstream location) or pull (i.e., downstream location) air into and through the animal chamber and respirometry flow-through system.
Subsample pump: To pull air through the analyzers, a small, stable, reliable pump is used.

Flow meters and flow controllers

Bubble flow meters: A simple, yet highly accurate way to measure flow rates invloves timing movement of bubbles of soap film up glass tubes between marks of known volume. The glass tube is connected at the bottom (for push systems) or at the top (for pull systems) to the air stream. A small rubber pipet bulb attached at the base of the tube acts as both a reservoir and delivery system for the soap bubbles. Operation is simple. First, wet the glass surface along the path bubbles travel (e.g., press the bulb so that copious amounts of soap are pushed up the glass by the air flow) to provide a virtually friction-free surface. Second, pinch the bulb so that one clean bubble is produced. With a stopwatch in hand, record the time required for the bubble to travel between marks on the glass. Note the volume recorded on the upper mark (e.g., 125 = 125 ml), divide the volume by the time required to travel between marks and the result is the flow rate (ml/sec).
Acrylic flow meters : Under some circumstances of high flow rates we may use simple acrylic flow meters (0 - 2.5 liters/min) to control the flow rates through the metabolic chambers. The meters are located upstream from the metabolic chambers. The flow meters are simple to use but should be calibrated twice daily for use in the respirometry system: once before recording begins (but after the animal has been sealed inside the chamber!!) and again at the end of the recording (before the animal is removed from the chamber!!). Calibration must be done with a bubble flow meter because the calibration marks on the acrylic meters are only approximate. For proper calibration of flow rates remember that both barometric pressure and temperature of the air streaming through the flow meter (which we assume to be equal to room temperature) must be recorded.
Mass flow meters: The equations required for calculating rates of oxygen consumption or carbon dioxide production assume that the flow rates into and out of the chambers are known exactly. We use mass flow meters which have the advantage of yielding flow rates independent of temperature and air pressure. Therefore, these flow rates can be considered to be corrected to standard conditions (Standard Temperature Pressure). We only measure and control flow at one location -- downstream from the chamber. Therefore, we must assume that the inflow and outflow rates are identical. However, during construction of the respirometry system, flow rate must be measured at all steps, across all connections, to verify integrety of flow.
Needle valves: Mass flow meters may be purchased with mass flow controllers which permit setting flow rates. These are expensive, however. Respirometry research often will attempt to measure more than one animal at a time, which would necessitate one chamber per animal and thus controlled flow through each chamber. An alternative and more cost-effective method to control flow would be via stainless steel or carbon steel needle valves. Needle valves plus mass flow meters provides a cost-effective means to achieve desired flow rates. The valves cost about $20.

Tubing and chambers

Tubing and connections : Various kinds of tubing can be use to connect the components of the respirometry system to and from the animal chamber. A variety of kinds of flexible tubing may be used, depending on the characteristics of the system. Acetyl, Bev-A-Line, Kynar, nylon, Tygon tubing and connectors may be used in regions of the system where oxidizing atmospheres are low (e.g., background levels of ozone only); teflon tubing would be recommended if ther is an expectation for appreciable amounts of ozone to be present because it is inert to ozone. Teflon tubes are more costly and lack flexibility.
Metabolic chambers: Chambers may be glass jars with rubber stoppers for lids; syringe barrels for small animals and insects; or constructed from Plexiglas. Chambers need to be constructed in a manner that yields rapid mixing of gases within the chamber. The simplest metabolic chamber may be a glass jar with a stopper. The stoppers are fitted with two ports: short extensions of teflon tubing are provided for line connections. Teflon tube extensions are pushed through the bulkhead and the line connection is finished by attaching a small hose clip to the base of the teflon tube extension. Additionally, you should provide an extension to the inlet port inside the jar -- this ensures that the animal's expiratory gases are not washed away by the in flow stream. The animal is sealed inside and the rubber stopper is held in place with velcro straps. Because we use an upstream system, any metabolic chamber leak will result in loss of animal air and, therefore, an underestimate of the animal's metabolic rate. When you close an animal inside a metabolic chamber, attention must be paid to the seal. To ensure tight seals before closing the lid, firmly work the stopper into the jar and make sure that it is even. Use 1-2 straps (2 are better) and pull tightly. Acrylic (Plexiglas) chambers will be constructed for some uses.
Scrubbing tubes: Water before and after the animal chamber must be removed. We use a large acrylic column of Drierite (8 mesh, relatively coarse) upstream (before the push pump, before the animal chamber) to dry incurrent airstream and several tubes with smaller mesh (10-20) Drierite to remove water after the animal chamber. To prepare a scrubbing tube, make sure there is a small amount of cotton at either end of the tube to prevent dust particles from travelling to the analyzers. Use small amounts of cotton, say around 0.005 g, just enough to keep the dust out of the tubing. Large amounts of cotton will block air flow when/if it gets damp. Pour the Drierite into the tube with a funnel, tap the tube on the bench to pack the grains tightly (to increase surface area - air + water rushes through loose Drierite, requiring frequent changes of scrubbers), and cap off with a small amount of cotton. To remove carbon dioxide before and after the animal chamber, Ascarite II is used. Ascarite II contains NaOH, which is caustic (so don't get any on your skin and keep away from water). A scrubbing tube is prepared by placing a small amount of cotton into the tube end, filling one third of the way with 10-20 mesh Drierite, adding a small amount of cotton, then an additional third of the tube with the Ascarite II, another layer of cotton, followed by more Drierite and capping the tube off with another small amount of cotton. Tap the tube on the bench as each layer is added to pack the grains. Note: Driereite can be used over and over again (after heating in an oven); Ascarite II is used once and will be considered a hazardous waste.

Analyzers

Carbon dioxide analyzer: CO₂ analyzers typically use infrared-based detection methods to take advantage of the fact that CO₂ will absorb infra-red light and re-emit light at slightly longer wavelengths. The panel meter on the analyzer displays over the entire 0.01 - 10% CO₂ range and a voltage output proportional to CO₂ concentration is also generated for data recording.
Oxygen analyzer: Modern O₂ analyzers use a fuel cell containing an acidic electrolyte, a heavy-metal anode and a thin gas-permeable membrane. Since the partial pressure of O₂ near the anode is zero, O₂ is driven by diffusion to the anode via the membrane at a rate proportional to ambient O₂ partial pressure. The fuel cell produces a voltage linearly proportional to the O₂ partial pressure at the membrane. As long as cabinet temperature is stable, and provided that air flow across the fuel cell is stable and within range.

Finally, a computer data acquisition and control system is needed. Instead of a chart recorder, continuous records of oxygen consumption and or carbon dioxide production are made with the assistance of an analog to digital convertor coupled to a computer. A variety of companies market such equipment, some specific for use in respirometry (e.g., Sable Systems, Qubit Systems, see also Warthog Systems).

References

Blaxter, K. 1989. Energy metabolism in animals and man. Cambridge University Press. ISBN 052136931
Nagy, K. A. 2005. Field metabolic rate and body size. Journal of Experimental Biology 208(9):1621-1625.
Weibel, E. R., and H. Hoppeler. 2005. Exercise-induced maximal metabolic rate scales with muscle aerobic capacity. Journal of Experimental Biology 208(9):1635-1644.
White, C. R., and R. S. Seymour. 2005. Allometric scaling of mammalian metabolism. Journal of Experimental Biology 208(9):1611-1619.

External links

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