The evolutionary tree is not observed here but it is possible to answer this question by observing which nucleotide is found in the root of the node. It indicates the first substitution.
<h3>What is an evolutionary tree?</h3>
A phylogenetic evolutionary tree is a diagram used to show the evolution of a given taxonomic group (for example, a group of species).
It is possible to trace the evolution of a given taxon by tracing the nucleotide substitution observed from a common ancestor.
In an evolutionary tree, the root of the node is represented by the common ancestor and therefore the presence of a particular nucleotide (either T or C) in that position can be considered as the ancestral character.
Learn more about evolutionary trees here:
brainly.com/question/2189834
Answer:
No, the child cannot inherit the disease.
Explanation:
The problem tells you that the man has a recessive allele for an inherited disease, but he has a normal phenotype. This means that the disease is recessive and in order for an individual to have the disease, they must have two recessive copies of the allele. The problem also tells you that the mother has a genotype that does not include this allele. With this information, you can do a punnet cross of BB (mother) x Bb (carrier father), and end up with the following possible genotypes: BB, Bb, BB, Bb. Therefore the child will not have the disease, but there is a 50% chance that the child will be a carrier for the disease.
I think that the answer this question would have to be c
D) take in nutrients because endocytosis is the process when a cell takes in food
