Answer:
The evolutionary mechanism that could be influencing the allele frequencies between both islands and the mainland population might be Founder Effect.
Explanation:
Genetic drift is the random change that occurs in the allelic frequency of a population through generations. The magnitude of this change is inversely related to the size of the original population. These changes produced by genetic drift accumulate in time and eventually, some alleles get lost, while some others might set. Genetic drift affects a population and reduces its size dramatically due to a disaster -bottleneck effect- or because of a population split -founder effect-. In <u>founder effect</u>, a new population originates when a few individuals who are coming from a bigger population carrying its genes, settle down in a new area and reproduce. This small population might or might not be genetically representative of the original one. Some rare alleles might be exceeded or might be completely lost. Consequently, when the small population increases in size, it will have a genetically different composition from the original one. In these situations, <u>genetic variability is reduced</u> and there exists the possibility of developing a peculiar allelic composition. If the number of individuals that originated the new population is low, the founder effect will be very extreme, because the effects of the genetic drift are inversely proportional to the original number of individuals.
<em>In the exposed situation, the evolutionary mechanism that could be influencing the allele frequencies between both islands and the mainland population might be Founder Effect. The fact that both islands are similar in their frequencies might be due to little genetic variation on island 1, or because dispersion to island 2 is a recent event on time. </em>
Answer:
Explanation:
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1. Diffusion
2. Osmosis
3. Facilitated Diffusion
Answer:
Details about DNA are given in the explanation section. Hope it will be helpful for you.
Explanation:
DNA, or deoxyribonucleic acid, is the hereditary element in humans and almost all other organisms. Nearly every cell in a person’s body has the same type of DNA. Most DNA is found in the cell nucleus (nuclear DNA), but a small quantity of DNA can also be found in the mitochondria (mitochondrial DNA or mtDNA).
The information in DNA is stored as a code made up of four chemical bases: adenine (A), guanine (G), cytosine (C), and thymine (T). Human DNA consists of about 3 billion bases, and more than 99 percent of those bases are the same type in all people.
DNA bases pair up with each other, A with T and C with G, to form units that are called base pairs. Each base is also attached to a sugar molecule and a phosphate molecule. A base, sugar, and phosphate are called a nucleotide. Nucleotides are arranged in two long strands that form a spiral called a double helix.
A valuable feature of DNA is that it can replicate, or make copies of itself. Each strand of DNA in the double helix can serve as a pattern for duplicating the sequence of bases.