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You observe a species of bird that, upon hatching, has contact with its parents only while being fed. You also never hear the parents sing during the feeding process. What would you propose about song production in this species of bird?
A. Song learning in this species is most likely learned behavior.
B. The period of imprinting is likely later in the bird's life.
C. This species does not hear.
<span>D. Song production in this species is most likely innate behavior.
the answer is d im pretty sure
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Answer:
The two circuits of the cardiovascular system are: Pulmonary Circuit and Systematic Circuit. The pulmonary circuit is shorter than the systemic and is responsible for carrying deoxygenated blood to the lungs from the right atrium, for oxygenation. The systemic circuit is longer and leaves the aortic artery, carrying oxygenated blood throughout the body and nutrients for survival. If less blood were pumped into the systemic circuit, this amount would not be sufficient to compensate for the organism's needs, with the corresponding consequences that this would entail.
It is said that the cardiovascular system is a closed system because blood travels inside a network of blood vessels without leaving them.
Answer:
mRNA: 3' AUG-AAU-GCU-GCC-GGU-GA-5'
amino acids : methionine, asparagine, alanine, arginine, proline
type of mutation: deletion, missense
Explanation:
The mRNA sequence is complementary to the DNA sequence. A always pairs with T, C always pairs with G. Except this is an RNA sequence not a DNA sequence, so T is replaced with U.
The mRNA sequence is translated into an amino acid sequence based on the triplet code. The triplet code for this sequence is shown in the attached picture. Each triplet signifies a specific amino acid. The codon can be identified from the table and placed in sequence. We can see that the new DNA strand has caused a new amino acid sequence. It has also left us with an incomplete sequence, as GA cannot signify an amino acid.
The type of mutation is a single base deletion. We can see that the base C is missing from the 9th amino acid in the original strand. As you can see, this has an ongoing affect on all the bases in the rest of the sequence, as it changes the way the sequence is organised into codons. This results in a missense mutation.
Is they are random changes I believe they should be mutations
