Answer:
b. average heterozygosity
Explanation:
From the available options:
a. nucleotide variability
b. average heterozygosity
c. average number of loci
d. geographic variability
Nucleotide variability represents a form of genetic variation that occur as a result of difference in nucleotide sequence of deoxy ribonucleic acid.
The locus is a region on the chromosome where genes are located. Average number of locus thus refers to total number of loci per total number of individuals in a population.
Geographic variability refers to difference in genetic traits across the various geographical distribution of a population.
Average heterozygosity is the percentage or proportion of heterozygous individuals for a trait within a population. It is a common measure of genetic variation in a population.
When a mutation occur within a population and this leads to the introduction of a new allele at a locus for which some individuals within the population are homozygous, it will directly affect the average heterozygosity of the population because more individuals will lose their homozygosity and become heterozygous.
<em>The correct option is b.</em>
Cells of various types have different functions because cell structure and function are closely related. It is apparent that a cell that is very thin is not well suited for a protective function.
The addition of acetyl groups to histones is associated with chromatin condensation and and higher levels of gene expression
The parotid duct empties into the vestibule at the level of the second upper molar.
Around the back of your lower jaw is where the parotid gland is located. Saliva then passes via a tube known as the parotid duct. The duct's opening is where the saliva spills into your mouth. Different factors might cause the parotid duct to become clogged. The region may swell up as a result of this.
Each gland's front faces a lengthy excretory channel called the parotid duct, which emerges just beneath the masseter muscle. The duct enters the mouth by the buccinator muscle and opens on the inner cheek surface, typically next to the maxillary second tooth
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Answer:
roan coat color in horses
Explanation:
Codominance is one of the Non-mendelian inheritance patterns in genetics i.e. does not follow Mendel's principles of inheritance. Codominance is a phenomenon whereby an allele is neither dominant nor recessive to another in a gene i.e. one allele is not phenotypically expressed over the other. Hence, both alleles are simultaneously expressed in their heterozygous state.
An example of codominance is the roan coat color in horses where the colored (B) and white (W) alleles are both dominant in the coat color gene, hence, the horse expresses both black and white coat phenotypes known as ROAN (BW). The black and white alleles are said to be CODOMINANT.
