Answer:
Explanation:
The sickle cell allele is recessive. Hence, in order for any child of the couple to have sickle cell anemia, such a child will have to inherit an affected allele each from the two parents. This means that both the father and the mother must have affected alleles in their genotypes. In other words, two sickle cell alleles are required for the abnormality to manifest.
Let us assume that the sickle cell allele is represented by S and the normal allele is represented by A.
Now, it is established that the mother has sickle cell anemia, her genotype would be SS. The father does not have sickle cell, his genotype can either be AA or AS.
Assuming the genotype of the father is AA:
SS x AA
AS AS AS AS
<em>All the children would be normal in this case.</em>
Assuming that the genotype of the father is AS
SS x AS
AS SS AS SS
<em>50% of the children would have sickle cell while the remaining 50% would be normal.</em>
<u>Therefore, in order to produce children with sickle cell, the father has to be AS, otherwise, he has to be AA.</u>
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Answer:
A is a eukaryotic cell while B is a prokaryotic cell
Explanation:
The researcher can conclude that <u>cell A is eukaryotic while cell B is prokaryotic.</u>
In eukaryotic cells, the <u>DNA is located majorly in the nucleus and the replication of the DNA happens in the nucleus</u>. Hence, it is only logical to find segments of new DNA in the nucleus of cell A during replication.
<u>Prokaryotic cells, however, lack a nucleus</u>. Their DNAs lie freely within the cytoplasm. This thus means that replication can only happen in the cytoplasm. Hence, it follows logically to find a new DNA segment in the cytoplasm of cell B.
Answer:
<u>Areas where lava recently flowed, a glacier retreated, or a sand dune formed.</u>
Explanation:
I don't know if this'll help you, but I think that should be somewhat about primary succession.
