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zheka24 [161]
2 years ago
6

Studies in which the suprachiasmatic nucleus (SCN) was surgically removed from laboratory mammals demonstrated that the SCN is r

equired for circadian rhythms. But these studies did not reveal whether circadian rhythms originate in the SCN. To answer this question, researchers performed an SCN transplant experiment on wild-type and mutant hamsters (Mesocricetus auratus). For wild-type hamsters, the period between cyclic peaks in activity is 24 hours in the absence of external cues. Hamsters homozygous for the τ (tau) mutation have a period lasting only about 20 hours. In this exercise, you will evaluate the design of this experiment and propose additional experiments to gain further insight. The researchers surgically removed the SCN from wild-type and τ hamsters. Several weeks later, each of these hamsters received a transplant of an SCN from a hamster of the opposite genotype. These transplants restored rhythmic activity in 80% of the hamsters. For hamsters in which an SCN transplant restored a circadian rhythm, the researchers measured the circadian period. The results are shown in the graph. Each red line represents the change in the measured period for an individual hamster. Part A - Understanding the experimental design In a controlled experiment, researchers manipulate one variable at a time. What was the experimental variable in this study?
Biology
1 answer:
Alex777 [14]2 years ago
3 0

Answer:

yo no se

Explanation:

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In an experiment, a control is an experiment or observation designed to minimize the effects of variables other than the independent variable. The introduction of a control increases the reliability of the results; often through a comparison between the control measurements and the other measurements.

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Yuki888 [10]

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p represents the frequency of the dominant allele (in decimal form) of a gene

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2pq = the frequency of heterozygous individuals in the population (decimal form)

q^2 = the frequency of homozygous recessive in the population (decimal form)

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Trava [24]

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Both Watson-Crick and Pauling's DNA models considered that DNA nitrogenous bases (i.e., Adenine, Cytosine, Thymine and Guanine) contain the genetic information that determines the characteristics of living organisms. Moreover, both DNA models also considered that nitrogenous base composition varies between species, as well as the arrangement of these bases in the DNA chain also varies between species. Based on these features, Linus Pauling considered that a model where nitrogenous bases would be arranged on the outside of the DNA molecule would be easier for the DNA molecule to be replicated, transcribed, or repaired. Although incorrect, Pauling's DNA triple helix model was fundamental to develop the helical (double-stranded) structure of DNA, which was finally discovered by Watson and Crick in 1953.

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