homologous structures are similar structures in different organisms that have a common evolutionary origin an example is

ATI TEAS 7

TEAS Test 7 science

1. Homologous structures are similar structures in different organisms that have a common evolutionary origin. An example is:

A. Butterfly wings and bird wings (analogous structures with different origins)
B. The arm of a human, the wing of a bat, and the flipper of a whale
C. The eyes of an octopus and a human (convergent evolution with different origins)
D. The stinger of a bee and the barb of a cactus (unrelated structures)

Correct answer: B

Rationale: Homologous structures are similar structures found in different organisms that share a common evolutionary origin. The arm of a human, the wing of a bat, and the flipper of a whale are all examples of homologous structures. Despite serving different functions, they share a common underlying structure due to their evolutionary relationship, evidencing a shared ancestry. These structures are modified over time to suit the specific needs of each species. Option A (Butterfly wings and bird wings) refers to analogous structures with different origins. Option C (The eyes of an octopus and a human) describes convergent evolution where traits evolve independently. Option D (The stinger of a bee and the barb of a cactus) are unrelated structures.

2. What is the end product of glycolysis?

A. Lactic acid
B. ATP
C. NADPH
D. Pyruvic acid

Correct answer: D

Rationale: The correct answer is D: Pyruvic acid. The end product of glycolysis is pyruvic acid, not lactic acid, ATP, or NADPH. Pyruvic acid is a key intermediary in cellular respiration and can be further metabolized to produce energy through processes like the citric acid cycle and oxidative phosphorylation. Lactic acid is produced in the absence of oxygen during fermentation, ATP is a product of cellular respiration but not the direct end product of glycolysis, and NADPH is generated in other metabolic pathways such as the pentose phosphate pathway, not in glycolysis.

3. Which statement correctly matches the valve with its function in the heart?

A. The aortic valve allows oxygenated blood to flow from the left ventricle to the rest of the body.
B. The mitral valve opens to allow blood flow from the left atrium to the left ventricle.
C. The pulmonic valve allows deoxygenated blood to flow from the right ventricle to the pulmonary artery.
D. The tricuspid valve allows deoxygenated blood to flow from the right atrium to the right ventricle.

Correct answer: A

Rationale: The correct answer is A. The aortic valve allows oxygenated blood to flow from the left ventricle to the rest of the body. When the left ventricle contracts, the aortic valve opens to allow blood to be pumped into the aorta, the body's main artery that carries oxygen-rich blood to various parts of the body. Choices B, C, and D are incorrect because they do not match the described functions of the mitral, pulmonic, and tricuspid valves, respectively. The mitral valve controls the flow of blood between the left atrium and left ventricle, the pulmonic valve regulates the flow of blood from the right ventricle to the pulmonary artery, and the tricuspid valve manages the blood flow between the right atrium and right ventricle.

4. Tendonitis is an inflammation of which part of the body?

A. Muscles
B. Tendons
C. Ligaments
D. Cartilage

Correct answer: B

Rationale: Tendonitis specifically refers to the inflammation of tendons, which are the thick cords that connect muscles to bones. The correct answer is tendons. Choice A, muscles, are not affected in tendonitis, but rather in myositis, which is the inflammation of muscles. Ligaments (Choice C) connect bones to other bones, while cartilage (Choice D) is a smooth and flexible tissue that covers the ends of bones at a joint. Therefore, the correct term for inflammation of tendons is tendonitis.

5. What is the term for a genetic disorder caused by a mutation in a mitochondrial gene?

A. Autosomal dominant disorder
B. Autosomal recessive disorder
C. Sex-linked disorder
D. Mitochondrial disorder

Correct answer: D

Rationale: A) Autosomal dominant disorder: This type of genetic disorder is caused by a mutation in one copy of an autosomal gene. It is not related to mitochondrial gene mutations. B) Autosomal recessive disorder: This type of genetic disorder is caused by mutations in both copies of an autosomal gene. It is not related to mitochondrial gene mutations. C) Sex-linked disorder: This type of genetic disorder is caused by mutations in genes located on the sex chromosomes (X or Y). It is not related to mitochondrial gene mutations. D) Mitochondrial disorder: Mitochondrial disorders are genetic disorders caused by mutations in genes located in the mitochondria, the energy-producing structures within cells. These disorders are inherited maternally and can affect various organs and systems in the body due to the role of mitochondria in energy production.