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Elis [28]
1 year ago
7

In a community a species of birds has some individuals with a different size and others which statement correctly explains how p

hysical differences in beaks would develop?
Biology
1 answer:
krok68 [10]1 year ago
3 0

Physical differences in beaks of birds would develop as a result of different environmental changes.

<h3>What is Evolution?</h3>

This is described as the process in which heritable characteristics are changed in species over successive generations. This occurs as a result of natural selection in which the traits suitable for survival are passed to the offspring.

This is usually as a result of a change in the environmental factors which ensures that the organisms are able to adapt so as not to die out and go extinct in this type of scenario.

Read more about Evolution here brainly.com/question/12271572

#SPJ1

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velikii [3]

Answer:

the group number is 2

Explanation:

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2 years ago
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An individual with Huntington disease has two normal parents. What are plausible explanations for this pattern of inheritance? C
Vitek1552 [10]

Answer and Explanation:

The Huntington disease is caused by a mutation in the gene that codifies for the Huntingtin protein (Htt). The mutation produces an altered form of the protein leading to the neuron´s death in certain areas of the brain.

The Huntington disease characterizes for being,

  • Hereditary, passing from generation to generation. To express the disease, a person must have been born with an altered gene.
  • Autosomal, affecting men and women equally, because the mutated gene is located on an autosomal chromosome.
  • Dominant, which means that by getting only one copy of the altered gene coming from any of the parents, the receiving person will express the disease. The mutation in the gene dominates over the normal gene copy.
  • Expressed by heterozygosis. Most people affected by the disease are heterozygous, with a normal copy and a mutated copy.

There are just a few cases all around the world (3% approximately) in which the disease is expressed with no family history. The progenitors are not affected by the mutation. These cases are very rare and are called <u>"de-novo" mutations.</u> A new mutation is spontaneously produced and it is not inherited from any of the parentals. It consists of an increase in the number of CAG repetitions. In a normal person, the number of CAG repetitions is less than 35. When there are 40 or more repetitions it occurs the disease. But when there are between 35 and 39 repetitions, the penetrance of the disease is incomplete. This is a "gray zone". Those alleles that fall in the gray zone are unstable and might produce the HD. Individuals with these unstable alleles have a tendency to increase the number of repetitions from generation to generation until the number reaches 40 repetitions and the person expresses the disease. This <u>usually occurs in the paternal germinal line</u>, as it is particularly unstable in sperm and probably meiosis greatly affects their instability, causing an increase in the number of CAG repeats.

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Explanation:

sorry if its incorrect.

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