The answer is a C3 fixation.
Plants are located in different regions with a different condition, so they had to adapt the carbon fixation. There are three types of carbon fixation in plants - C3, C4, and CAM fixation. C3 and C4 plants open their stomata during the day while CAM plants open stomata during the night.
Plants in arid locations use CAM carbon fixation because of adaptation to water deficiency. In CAM plants, stomata are closed during the day and water loss is reduced. In the night when is colder, stomata open and carbon dioxide enters through stomata. In C4 carbon fixation, there is also adaptation to high temperatures thanks to enzymes that increase the rates of photorespiration, unlike the C3 fixation.
Answer:
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"a heart on the run keeps a hand on a gun you can't trust anyone"
Answer:
Enzyme-controlled chemical reactions combining carbon dioxide and glucose water. The photosynthetic rate is affected by the temperature much like any other enzyme-controlled reaction.
Explanation:
At low temperatures, the number of molecular collisions between enzymes and substrates limits the photosynthetic rate. Enzymes are denatured at high temperatures.
Enzymes are protein molecules used in biological reactions by living organisms. The proteins are folded in a very specific form, which enables them to effectively bind to the molecules of interest. The enzymes used for photosynthesis perform less efficiently at a low temperature between 32 and 50 degrees Fahrenheit 0, 10, and 10 degrees Celsius, which lowers the photosynthesis rate.This will lead to lower glucose synthesis and slow growth. In the case of plants in a greenhouse, this is prevented by installing a greenhouse heater and thermostat.
Huntington’s disease is an autosomal dominant disease, thereby the probability that a child will develop the disease is 100% if one parent has one mutated allele (Option D).
<h3>What is an autosomal dominant disease?</h3>
An autosomal dominant disease is any inherited disorder that is expressed in the phenotype in heterozygous individuals.
The mutated allele that causes autosomal dominant diseases is dominant and masks the expression of the recessive allele.
In conclusion, the probability that a child will develop the disease is 100% if one parent has one mutated allele (Option D).
Learn more about autosomal dominant diseases here:
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