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Oxygen AnalyzerS (Gas Phase)

Qubit O2 gas analysers for applications in life science research, education, environmental monitoring and industry. Sensors feature temperature and pressure compensation and offer variations in concentration range, response and resolution. Gas-phase Oxygen analysers include: 

  • Q-S108 O2 Analyser, with build in pump, pressure sensor and field case
  • Q-S102 O2 Analyser, module
  • Q-S104 Differential O2 Analyser (DOX), for highest accuracy in differential mode.

Q-S108 Absolute O2 Analyser

Q-S108 Absolute Oxygen Analyzer
Q-S108 Absolute O2 Analyzer

Q-S108 Absolute O2 Analyser. The most versatile, accurate and cost-effective oxygen analyser on the market. The use of a fuel cell sensor that operates at ambient temperature sets it apart from its counterparts that rely on power-hungry zirconium sensors that require an on-board heater. The sensor is equipped with acidic electrolytes and a Teflon diffusion membrane, ensuring accurate pO2 measurements over the entire range. For animal and human respirometry, the Q-S108 Absolute O2 analyser integrates seamlessly with the Q-S158 CO2 analyser for measurement of the respiratory quotient. It can be configured in a stop-flow or closed gas exchange system for respirometry on smaller or less active organisms. Calibration is a breeze, requiring only dry ambient air (optimal for the most stringent measurements is the use of an N2 zero gas). The Q-S108 maintains linearity over its full dynamic range. Simplify the process further by using the Q-S108 O2 Analyser with the Q-C901 Logger Pro software, or other compatible data acquisition software.

Q-S108 - Features

  • Switchable ranges of 0-25% and 0-100% O2
  • Integrated pressure sensor and signal correction
  • Integrated gas pump
  • Built-in temperature control and compensation
  • Analogue outputs 0-5V for O2 and Pressure; O2 output displayed in % or kPa, Pressure output displayed in kPa
  • Fast response time (90%): 12 sec
  • Weatherproof case
  • Stand alone or with optional software

Options

  • Battery pack, for field use (optional)
  • Q-C901 LoggerPro Software (recommended)

See below for Q-S108 Specifications, and References.

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Please contact us for the manual and further information.


Q-S102 O2 Analyser

Q-S102 O2 Analyzer
Q-S102 O2 Analyzer

Q-S102 O2 Analyser. Measures oxygen concentration in flow-through gas exchange systems, offering a range of 0-25% or 0-100% with an accuracy of 0.21%. The analyser measures the total gas pressure at the O2 sensor. Perfect for assessing O2 uptake in organisms with high metabolic rates, the Q-S102 excels in an open flow system configuration. For organisms with lower metabolic rates, it seamlessly transitions to a closed flow system, allowing the calculation of O2 uptake rate from the slope of O2 decline in the system. Operating the Q-S102 O2 analyser requires a data interface with two analogue signal ports and dedicated software; using the Q-C610 LabQuest Mini data interface with Q-C901 Logger Pro Software is recommended. The Q-S102 O2 Analyser is a key component in Q-Box Research Packages:

  • Insect Respirometry Q-RP1LP Package,
  • Q-RP2LP Animal Respirometry System,
  • Q-NF1LP Nitrogen Fixation Package.

Q-S102 - Features

  • Switchable ranges of 0 - 25 kPa and 0 - 100 kPa O2; 0 - 5 V analogue output at both ranges
  • Built-in gas pressure sensor
  • Galvanic cell technology
  • Compact and portable

Optional

  • Battery pack, for field use
  • Pump, flow meter, etc.
  • Data Interface
  • LoggerPro Software
Measurement Principle Q-S108 / Q-S102
O2 Sensors
OPEN

The O2 analysers have  a galvanic cell (a lead-oxygen battery) consisting of a lead anode, an O2 cathode and an acid electrolyte. It also contains an O2-permeable Teflon FEP membrane with a gold electrode bonded to its surface; oxygen diffusing through the membrane is electrochemically reduced at the gold electrode. A resistor and a thermistor (for temperature compensation) are connected between the anode and cathode. The output of the instruments is proportional to the current flowing through the resistor and thermistor and this is proportional to the pO2 in contact with the Teflon membrane. 

Specifications Q-S108 / Q-S102 OPEN

Operating principle: Acid Electrolyte, Teflon Diffusion Membrane; influence by other gases: Ammonia and Ozone

Detection Range: 0-25% and 0-100 %O2 (linear)

Analog Output: 0 to 5 Volt

Resolution / Accuracy: ±40 ppm / ±0.21% of Full Scale

Response Time (90%): 12 s

Life Expectancy of sensor: 3-5 years, sensor easily replaceable

Gas pump: 0-650 ml min-1, default setting of 100 ml min-1; minimumflow: 5 mL min-1

Built in total gas pressure reading at the sensor and correction of signal

Pressure Range: 50,6 kPa to 152 kPa; pressure effect - Output voltage changes proportionally

Operating Temperature: 5 to 40°C; built in temperature control and correction of signal

Shock Resistant: to 2.7 G; avoid strong vibration

Power Supply: 12 Volt

Dimensions: 27.7 x 25.5 x 11.2 cm (L x W x H)

Weight: 2.45 kg (Q-S108) / 1.35 kg (Q-S102)

 

 

Optional:

Data interface and software,

Battery pack for field use

References Gas-Phase Oxygen Sensors OPEN

  • Soliz J. et al. Erythropoietin regulates hypoxic ventilation in mice by interacting with brainstem and carotid bodies. The Journal of Physiology 568:559-571 (2005)
  • Bézy, Vanessa S., Roldán A. Valverde, and Craig J. Plante. “Olive Ridley Sea Turtle Hatching Success as a Function of Microbial Abundance and the Microenvironment of In Situ Nest Sand at Ostional, Costa Rica.” Journal of Marine Biology 2014 (2014)
  • Willms JR, Dowling AN, Dong ZM, Hunt S, Shelp BJ, Layzell DB The simultaneous measurement of low rates of CO2 and O2 exchange in Biological Systems. Anal. Biochem. 254: 272-282 (1997)
  • Willms JR, Salon C, Layzell DB Evidence for light-stimulated fatty acid synthesis in soybean fruit. Plant Physiol. 120: 1117-112 (1999)
  • Cen Y-P, Turpin DH, Layzell DB Whole-plant gas exchange and reductive biosynthesis in white lupin. Plant Physiol. 126: 1555-1565 (2001)
  • Amthor,JS, Koch GW, Willms JR, Layzell DB Leaf O2 uptake in the dark is independent of coincident CO2 partial pressure. J.Exp.Bot. 52: 2235-2238 (2001)
  • Davey, PA, Hunt S, Hymus GJ, DeLucia EH, Drake BG, Karnosky DF, Long SP Respiratory oxygen uptake is not decreased by an instantaneous elevation of [CO2], but is increased with long term growth in the filed at elevated [CO2]. Plant Physiol. 134: 520-527 (2004)
  • John P. Isanhart, F. M. Anne McNabb and Philip N. Smith. Effects of perchlorate exposure on resting metabolism, peak metabolism, and thyroid function in the prairie vole (Microtus ochrogaster). Environmental Toxicology and Chemistry Vol 24, Issue 3, p678–684 (2005)
  • Efrat Elimelech and Berry Pinshow. Variation in food availability influences prey-capture method in antlion larvae. Ecological Entomology Vol 33, Issue 5, p652–662 (2008).
  • Leakey ADB, Xu F, Gillespie KM, McGrath JM, Ainsworth EA, Ort DR. Genomic basis for stimulated respiration by plants growing under elevated carbon dioxide. PNAS Vol. 106 Number 9 pg.3597-3602 (2009)
  • Meaghan Jenkins and Mark A. Adams. Vegetation type determines heterotrophic respiration in subalpine Australian ecosystems Global Change Biology Vol 16,p209–219 (2010).
  • Gifford ME, Clay TA, Peterman WE. The Effects of temperature and activity on Intraspecific Scaling of Metabolic rates in a lungless Salamander. JEZ-A Ecological and Integrative Physiology. V 319, pg. 179-236 (2013)
  • Gifford ME, Young VKH Limited Capacity for acclimation of thermal physiology in a salamander, Desmognathus brimleyorum Journal of Comparative Physiology 183, pg 409-418 (2013)
  • Meier IC, Angert A, Falik O, Shelef O, Rachmilevitch S. Increased root oxygen uptake in pea plants responding to non-self neighbours. Planta 238, pg. 577-586 (2013)
  • Glassey B, Gunson M, Muir R Context‐dependent costs and constraints of begging and non‐begging activity by common grackle nestlings at the scale of the nanoclimate. Functional Ecology V. 28, pg. 904-912 (2014)
  • Artacho P, Saravia J, Decenciere Ferrandiere B, Perret S, Le Galliard JF. Quantification of correlational selection on thermal physiology, thermoregulatory behaviour, and energy metabolism in lizards. Ecology and Evolution V5, pg. 3600-3609 (2015)
  • Pak NM, Rempillo O, Norman AL & Layzell DB Early atmospheric detection of carbon dioxide from capture and storage sites. Journal of the Air and Waste Management Association V66, pg. 739-747 (2016)
  • Karvansara PR, Razavi SM Physiological and biochemical responses of sugar beet (Beta vulgaris L) to ultraviolet-B radiation. PeerJ 7:e6790 https://doi.org/10.7717/peerj.6790 (2019)
  • Najafi S, Medhi Razavi S, Khoshkam M, Asadi A Effects of green synthesis of sulfur nanoparticles from Cinnamomum zeylanicum barks on physiological and biochemical factors of Lettuce (Lactuca sativa). Physiology and molecular biology of plants 26, 1055-1066 (2020)
  • Sadie B. Barr and Jonathan C. Wright. Postprandial energy expenditure in whole-food and processed-food meals: implications for daily energy expenditure. Food Nutr Res. Vol 54 (2010).
  • Shannon M. Fernando, Pengcheng Rao, Lee Niel, Diptendu Chatterjee, Marijana Stagljar andD. Ashley Monks. Myocyte Androgen Receptors Increase Metabolic Rate and Improve Body Composition by Reducing Fat Mass. Endocrinology Vol. 151, Number 7, p3125-3132 (2010).
  • T. Todd Jones, Richard D. Reina, Charles-A. Darveau and Peter L. Lutz. Ontogeny of energetics in leatherback (Dermochelys coriacea) and olive ridley (Lepidochelys olivacea) sea turtle hatchlings. Comparative Biochemistry and Physiology – Part A: Molecular & Integrative Physiology Vol 147, Issue 2, p313-322 (2007).
  • R.Refinetti. Absence of circadian and photoperiodic conservation of energy expenditure in three rodent species. Journal Of Comparative Physiology B: Biochemical, Systemic, And Environmental Physiology Vol 177, Number 3, p309-318 (2007).
  • Edwin R. Price, Frank V. Paladino, Kingman P. Strohl, Pilar Santidrián T., Kenneth Klann and James R. Spotila. Respiration in neonate sea turtles. Comparative Biochemistry and Physiology, Part A Vol 146, Issue 3, p422–428 (2007).
  • David Nestel, Esther Nemny-Lavy, Sheikh Mohammad Islam, Viwat Wornoayporn and Carlos Cáceres. Effects Of Pre-Irradiation Conditioning Of Medfly Pupae (Diptera: Tephritidae): Hypoxia And Quality Of Sterile Males. Florida Entomologist Vol 90 Number 1, p80-87 (2007).
  • Muleme HM, Walpole AC and Staples JF. Mitochondrial metabolism in hibernation: metabolic suppression, temperature effects, and substrate preferences. Physiol Biochem Zool. Vol 79, Number 3, p474-83 (2006).
  • Tammy Chan and Warren Burggren. Hypoxic incubation creates differential morphological effects during specific developmental critical windows in the embryo of the chicken (Gallus gallus). Respiratory Physiology & Neurobiology Vol 145, Issues 2-3, Pages 251-263 (2005).
  • Tapio Eeva, Esa Lehikoinen, and Mikko Nikinmaa. Pollution-Induced Nutritional Stress In Birds: An Experimental Study Of Direct And Indirect Effects. Ecological Applications Vol 13, Issue 5, p1242–1249 (2003).
  • Frances D. Duncan and Marcus J. Byrne. Respiratory airflow in a wingless dung beetle. The Journal of Experimental Biology Vol 205, p2489–2497 (2002).
  • C. J. Bernacchi, E. L. Singsaas, C. Pimentel, A. R. Portis Jr and S. P. Long. Improved temperature response functions for models of Rubisco-limited photosynthesis. Plant, Cell & Environment Vol 24, Issue 2, p253–259 (2001).
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Q-S104 Differential O2 Analyser (DOX)

Q-S104 DOX Differential O2 Analyzer
Q-S104 Differential O2 Analyzer (DOX)

Q-S104 Differential O2 Analyser (DOX). The world's only differentially patented oxygen analyser with an impressive ±1 ppm O2 resolution in ambient air conditions. The Q-S104 DOX can measure real-time oxygen consumption rates in tiny insects and monitor photosynthetic oxygen production from a single intact leaf. The Q-S104 Differential O2 Analyser has the widest dynamic range of any gas analyser on the market - at lower resolution it can even assess O2 exchange in larger mammals. Seamlessly integrated with a CO2 analyser (Q-S157) in an open gas exchange system, this powerful tool facilitates Gas Exchange Quotient measurements at a low range. Operating in true differential mode, the Q-S104 DOX Differential Oxygen Analyser offers ranges of ±100, ±300, and ±1000 Pa O2. It simultaneously monitors both the reference and sample oxygen sensors and has an automatic reference-sample function that provides measurements of any oxygen difference. This flexibility allows measurement of oxygen exchange in different species by selecting the appropriate range setting. Unlike many high resolution gas analysers that require calibration with expensive standard gases or complicated mixing systems, the Q-S104 DOX O2 analyser uses ambient air and employs a simple pressure-based calibration method. Calibration is not only simple, but also remarkably accurate, maintaining perfect linearity over the full dynamic range of the analyser and calibration gas. The use of air as the 'calibration gas' makes calibration cost-effective and easily accessible. Applications include: Single leaf photosynthetic O2 exchange, leaf dark respiration rate (for CO2 see also the Q-CO650 photosynthesis package), Insect Respiratory O2 Consumption, Small & large animal respirometry, etc.

Q-S104 DOX - Features

  • ±1 ppm oxygen resolution vs. air (0.0001%!)
  • Largest dynamic range of any oxygen analyser
  • Simple calibration, without special calibration gases
  • Separate analogue signals for reference and sample pO2
  • Automatic reference sample function
  • Analogue signals for differential pO2, absolute pressure, differential pressure, sample and reference cell temperature, instrument temperature

Option:

  • Use with NIDR CO2 analysers for powerful measurements of the respiratory quotient
Specification Q-S104 DOX OPEN

Power Supply: 12V 115/220 VAC
Oxygen Sensor life: 3 to 5 years (easily replaceable)
Analog Output: 0 to 5 V (recommended: 16-Bit Analog to Digital converter)

 

Absolute Signals
Signal Range Reference and Sample: 0 to 100% O2
Resolution / Accuracy: 0.001%O2 / ±0.002% O2
Response Time: T90 = 20 s, partial pressure measurement
Pressure Signal Range / Resolution: 15 to 115 kPa / 0.01 kPa 
Pressure Signal Noise / Accuracy: < 0.01 kPa / 1% of Full Scale
Reference and Sample Air Temperature Signals Resolution / Accuracy: 0.01°C / ±0.1°C
Oven Temperature Signal Range / Resolution / Accuracy: 10 to 50°C / 0.01°C / ±0.1°C

 

Differential Signals
Oxygen Signal Range: 1000 to 10000 ppm O2 (user defined)
Oxygen Signal Resolution / Accuracy: 1 ppm O2 / ±2.5 ppm O2
Oxygen Signal Response Time: T90 = 20 s, partial pressure measurement.
Pressure Signal Range / Resolution / Accuracy: ±620 Pa / 1 Pa / 1% of Full Scale
Reference and Sample Air Temperature Signals Range: 0 to 50°C

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Gas Switching Multiplexing Systems 4 or 8 channels

For O2 analyser switching between 4 or 8 channels in open or stop flow modes, the fitting gas switching systems are available.


Q-S159 CO2 and O2 Analyzer

For parallel measurements of CO2 and O2 concentrations in the gas-phase consider the Q-S159 CO2 and O2 Analyser, or the Q-RP1LP Low Range or Q-RP2LP High Range Research Packages.


OX1LP Dissolved Oxygen Package

For O2 measurements in the liquid phase, the OX1LP Dissolved Oxygen Package, or Dissolved Oxygen Electrodes are available.



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