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Diekoloreoluwa Oyegunle

Faythe Miller

Christian chukwufumnanya Eluemelem

Q10 (temperature coefficient)

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The Q10 temperature coefficient is a measure of temperature sensitivity based on biological or chemical reactions. It is usually defined as the rate ratio of a given process taking place at temperatures differing by 10 units (℃ or K)[1]. Q10 can be used to measure temperature sensitivity in animals or plants. However, conclusions drawn by different researchers from the use of this coefficient are not universal and are not always consistent with each other. The Q10 coefficient is described by exponential laws instead of power laws, which leads to deviations from linearity in the Arrhenius plots [2]. The arrhenius plot is derived from the arrhenius equation further explained in this literature[3]. A temperature increase by 10 units does not entail the doubling or tripling of the

A plot of the temperature dependence of the rates of chemical reactions and various biological processes, for several different Q10 temperature coefficients.
A plot illustrating the dependence on temperature of the rates of chemical reactions and various biological processes, for several different Q10 temperature coefficients. The rate ratio at a temperature increase of 10 degrees (marked by points) is equal to the Q10 coefficient.

rate of a given process, as is usually assumed in the relevant literature[4]

The Q10 is calculated as:

where;

R is the rate
T is the temperature in Celsius degrees or kelvin.
R2 has to be Where T2 is greater than T1, (T2 > T1)
R1 is the rate of the reaction at the lower temperature, T1
R2 is the rate of the reaction or biological process at the higher temperature, T2
It is also important to note that the rates, R1 and R2 must be measured using the same unit, i.e., if R1 is measured in m/s, then measured also in m/s and not m/min.

Rewriting this equation, the assumption behind Q10 is that the reaction rate R depends exponentially on temperature:

Q10 is a unitless quantity, as it is the factor by which a rate changes, and is a useful way to express the temperature dependence of a process.

For most biological systems, the Q10 value is ~ 2 to 3.

Q10 Temperature Coefficient in Plants

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The Q10 temperature coefficient does not only exist in animals but exists in plants as well. Q10 in soils, roots and stems defines the temperature sensitivity of the plant in question [5]. Generally, researchers use Q10 when they are trying to measure temperature sensitivity of heterotrophic soil respiration. When measuring Q10 in plants it is important to note that it cannot be measured everywhere. Moreover, there is special knowledge about spatial patterns and regulating factors that are required [6]. Spatial patterns and regulating factors include the difference in geographical location, soil organic carbon and soil moisture levels.

Q10 Temperature Coefficient in Animals

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In some animals, Q10 can be measured using the muscles. The temperature of a muscle in ectothermic and endothermic animals have a significant effect on the velocity and power of the muscle contraction. Performance generally declines with decreasing temperatures and increases with rising temperatures[7]. To predict these changes, researchers use the Q10 temperature coefficient to

The effects of temperature on enzyme activity. Top - increasing temperature increases the rate of reaction (Q10 coefficient). Middle - the fraction of folded and functional enzyme decreases above its denaturation temperature. Bottom - consequently, an enzyme's optimal rate of reaction is at an intermediate temperature.

measure resting metabolic rate of the muscle. The Q10 coefficient represents the degree of temperature dependence a muscle exhibits as measured by contraction rates [1]. A Q10 of 1.0 indicates thermal independence of a muscle whereas an increasing Q10 value indicates increasing thermal dependence. Values less than 1.0 indicate a negative or inverse thermal dependence, i.e., a decrease in muscle performance as temperature increases[8].

Q10 values for biological processes vary with temperature. Decreasing muscle temperature results in a substantial decline of muscle performance such that a 10 degree Celsius temperature decrease results in at least a 50% decline in muscle performance [9]. Persons who have fallen into icy water may gradually lose the ability to swim or grasp safety lines due to this effect, although other effects such as atrial fibrillation are a more immediate cause of drowning deaths. At some minimum temperature biological systems do not function at all, but performance increases with rising temperature (Q10 of 2-4) to a maximum performance level and thermal independence (Q10 of 1.0-1.5). With continued increase in temperature, performance decreases rapidly (Q10 of 0.2-0.8) up to a maximum temperature at which all biological function again ceases [10].

Within vertebrates, different skeletal muscle activity has correspondingly different thermal dependencies. The rate of muscle twitch contractions and relaxations are thermally dependent (Q10 of 2.0-2.5), whereas maximum contraction, e.g., tetanic contraction, is thermally independent [10].

See also[edit]

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References[edit]

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  1. ^ a b Mundim, Kleber C.; Baraldi, Solange; Machado, Hugo G.; Vieira, Fernando M. C. (2020-09-01). "Temperature coefficient (Q10) and its applications in biological systems: Beyond the Arrhenius theory". Ecological Modelling. 431: 109127. doi:10.1016/j.ecolmodel.2020.109127. ISSN 0304-3800.
  2. ^ "Metal substitutions in carbonic anhydrase: A halide ion probe study". Biochemical and Biophysical Research Communications. 66 (4): 1281–1286. 1975-10-27. doi:10.1016/0006-291X(75)90498-2. ISSN 0006-291X.
  3. ^ Carvalho-Silva, Valter H.; Coutinho, Nayara D.; Aquilanti, Vincenzo (2019-05-29). "Temperature Dependence of Rate Processes Beyond Arrhenius and Eyring: Activation and Transitivity". Frontiers in Chemistry. 7: 380. doi:10.3389/fchem.2019.00380. ISSN 2296-2646. PMC 6548831. PMID 31192196.{{cite journal}}: CS1 maint: PMC format (link) CS1 maint: unflagged free DOI (link)
  4. ^ Reyes, Bryan A.; Pendergast, Julie S.; Yamazaki, Shin (2008-02-01). "Mammalian Peripheral Circadian Oscillators Are Temperature Compensated". Journal of Biological Rhythms. 23 (1): 95–98. doi:10.1177/0748730407311855. ISSN 0748-7304. PMC 2365757. PMID 18258762.{{cite journal}}: CS1 maint: PMC format (link)
  5. ^ Wang, Wenjie; Wang, Huimei; Zu, Yuangang; Li, Xueying; Koike, Takayoshi (2006-06-01). "Characteristics of the temperature coefficient, Q10, for the respiration of non-photosynthetic organs and soils of forest ecosystems". Frontiers of Forestry in China. 1 (2): 125–135. doi:10.1007/s11461-006-0018-4. ISSN 1673-3630.
  6. ^ Meyer, N.; Welp, G.; Amelung, W. (2018). "The Temperature Sensitivity (Q10) of Soil Respiration: Controlling Factors and Spatial Prediction at Regional Scale Based on Environmental Soil Classes". Global Biogeochemical Cycles. 32 (2): 306–323. doi:10.1002/2017GB005644. ISSN 1944-9224.
  7. ^ Anderson, C. V.; Deban, S. M. (2010-03-08). "Ballistic tongue projection in chameleons maintains high performance at low temperature". Proceedings of the National Academy of Sciences. 107 (12): 5495–5499. doi:10.1073/pnas.0910778107. ISSN 0027-8424.
  8. ^ Bennett, A. F. (1984-08-01). "Thermal dependence of muscle function". American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 247 (2): R217–R229. doi:10.1152/ajpregu.1984.247.2.R217. ISSN 0363-6119.
  9. ^ Deban, S. M.; Lappin, A. K. (2011-04-15). "Thermal effects on the dynamics and motor control of ballistic prey capture in toads: maintaining high performance at low temperature". Journal of Experimental Biology. 214 (8): 1333–1346. doi:10.1242/jeb.048405. ISSN 0022-0949.
  10. ^ a b Bennett, A. F. (1990-08-01). "Thermal dependence of locomotor capacity". American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 259 (2): R253–R258. doi:10.1152/ajpregu.1990.259.2.R253. ISSN 0363-6119.