Smaller cube (1 cm X 1 cm X 1 cm)
<span>The surface area of one side = 1 cm X 1 cm = 1 <span>cm2</span></span>
<span>There are 6 sides, total SA = 6 X 1 <span>cm2</span> = 6 <span>cm2</span></span>
<span>Volume = 1 cm X 1 cm X 1 cm = 1 cubic cm (1 <span>cm3</span>)</span>
<span>Surface to Volume Ratio = 6 <span>cm2</span>/1 <span>cm3</span> = 6 <span>cm2/cm3</span></span>
Larger cube (6 cm X 6 cm X 6 cm)
<span>The surface area of one side = 6 cm X 6 cm = 36 <span>cm2</span></span>
<span>There are 6 sides, the total SA = 6 X 36 <span>cm2</span> = 216 <span>cm2</span></span>
<span>Volume = 6 cm X 6 cm X 6 cm = 216 <span>cm3</span></span>
<span>Surface to Volume Ratio = 216 <span>cm2</span>/216 <span>cm3</span> = 1 <span>cm2/cm3</span></span>
<span> </span>
Answer:
The mentioned case is an illustration of the missense mutation. A missense mutation is a kind of nonsynonymous substitution, that is, it is a mutation in which a variation in a solitary nucleotide leads to the formation of a codon, which encrypts for a distinct kind of amino acid.
When a missense mutation takes place within a DNA, a modification in one of the RNA codon sequences results at the time of transcription. This change in codon will ultimately result in the formation of a different amino acid, which gets presented within a protein at the time of translation. Like in the given case, a change in codon resulted in the substitution of the amino acid tyrosine with an amino acid cysteine.
Answer:
C, there is genetic variation within the population
Explanation:
Answer:
The dihybrid ratio we expect in the offspring is 9:7.
Explanation:
This is an example of complementary gene interaction, which is the non allelic interaction or genes, where the prominent genes at heterozygous loci may complement each other by complementing recessive alleles at the respective loci.
So in this case of complementary gene interaction, the individuals that are A-bb or aaB- or aabb will have the same set of observable features (phenotype) but only A-B- individuals will how the dominant phenotype.
