ATI TEAS 7
ATI TEAS Science Questions
1. Which type of tissue connects muscles to bones?
- A. Ligaments
- B. Tendons
- C. Cartilage
- D. Muscles
Correct answer: B
Rationale: The correct answer is B: Tendons. Tendons connect muscles to bones, not bones to muscles. They play a crucial role in transmitting the force generated by muscles to move bones, enabling movement. Ligaments (choice A) connect bones to bones, providing stability to joints. Cartilage (choice C) is a connective tissue found in joints, providing cushioning and flexibility. Muscles (choice D) are responsible for generating force through contraction but do not directly connect muscles to bones.
2. The ureters are paired tubes that transport urine from the:
- A. Bladder to the urethra
- B. Kidneys to the bladder
- C. Urethra to the kidneys
- D. Skin to the kidneys
Correct answer: B
Rationale: The ureters are responsible for carrying urine from the kidneys to the bladder. Once urine is produced in the kidneys, it travels down the ureters to be stored in the bladder until it is eliminated from the body through the urethra. Therefore, the correct answer is B, 'Kidneys to the bladder.' Choices A, C, and D are incorrect as they do not accurately describe the function of the ureters in the urinary system. Choice A, 'Bladder to the urethra,' is incorrect because the ureters carry urine from the kidneys to the bladder, not from the bladder to the urethra. Choice C, 'Urethra to the kidneys,' is incorrect as the flow of urine is from the kidneys to the bladder via the ureters, not in the reverse direction. Choice D, 'Skin to the kidneys,' is unrelated to the urinary system; the ureters are not involved in transporting substances from the skin to the kidneys.
3. 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.
4. What is the process by which decomposers break down organic matter?
- A. Photosynthesis
- B. Bioremediation
- C. Decomposition
- D. Nitrification
Correct answer: C
Rationale: A) Photosynthesis is the process by which plants, algae, and some bacteria convert light energy into chemical energy to produce glucose from carbon dioxide and water. This process is not related to the breakdown of organic matter by decomposers. B) Bioremediation is the use of living organisms to clean up contaminated environments. While it involves the use of microorganisms to break down pollutants, it is not specifically focused on breaking down organic matter. C) Decomposition is the process by which decomposers such as bacteria, fungi, and other organisms break down organic matter into simpler substances. This process is essential for nutrient recycling in ecosystems. D) Nitrification is the biological oxidation of ammonia or ammonium to nitrite followed by the oxidation of nitrite to nitrate by nitrifying bacteria. This process is part of the nitrogen cycle and is not directly related to the breakdown of organic matter.
5. Where does glycolysis occur within the cell?
- A. Cytosol
- B. Nucleus
- C. Mitochondria
- D. Endoplasmic reticulum
Correct answer: A
Rationale: Glycolysis occurs in the cytosol, the liquid component of the cytoplasm, not in the nucleus, mitochondria, or endoplasmic reticulum. It is the initial step in cellular respiration and involves the breakdown of glucose into pyruvic acid. The process takes place in the cytosol as it does not require membrane-bound organelles like the mitochondria or endoplasmic reticulum for its completion.
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