organisms that break down dead organisms and return nutrients to the environment are called
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ATI TEAS 7

TEAS 7 practice test free science

1. What are organisms that break down dead organisms and return nutrients to the environment called?

Correct answer: B

Rationale: Decomposers are essential organisms in the ecosystem as they break down dead organisms and organic matter, such as bacteria, fungi, and some insects. By decomposing complex organic materials into simpler forms, they release nutrients back into the environment for other organisms to utilize. Producers (option A) are organisms that generate their own food through photosynthesis; consumers (option C) are organisms that feed on other organisms for energy, and parasites (option D) are organisms that live on or in another organism, benefiting at the host's expense rather than breaking down dead organisms for nutrient recycling.

2. Which structure in the heart is responsible for pumping oxygenated blood to the body?

Correct answer: B

Rationale: The left ventricle is the chamber responsible for pumping oxygenated blood from the heart to the body. It receives oxygen-rich blood from the left atrium and contracts to push this blood out to the rest of the body through the aorta. The right ventricle pumps deoxygenated blood to the lungs for oxygenation, making choices A, C, and D incorrect for this function. Therefore, the correct answer is B, the Left ventricle.

3. How do spindle fiber dynamics and microtubule attachment regulate cell cycle checkpoints?

Correct answer: D

Rationale: A) Misaligned chromosomes fail to attach to microtubules, triggering a delay in anaphase onset: Proper attachment of chromosomes to spindle fibers is essential for accurate segregation of genetic material during cell division. Misaligned chromosomes that fail to attach to microtubules can lead to delays in anaphase onset, allowing the cell to correct errors before proceeding with division. B) The presence of unattached kinetochores on the centromeres sends a signal to pause cell cycle progression: Kinetochores at the centromeres help attach chromosomes to spindle fibers. When kinetochores are unattached or improperly attached to microtubules, they signal the cell to pause cell cycle progression, ensuring proper chromosome alignment before division. C) Microtubule instability and rapid depolymerization lead to the activation of checkpoint proteins: While microtubule dynamics are crucial for cell division, microtubule instability and rapid depolymerization can disrupt chromosome attachment. However, this mechanism is not directly related to the activation of cell cycle checkpoint proteins, making this statement incorrect. Therefore, choices A and B accurately describe how spindle fiber dynamics and microtubule attachment regulate cell cycle checkpoints, making option D the correct answer.

4. Where would a nonpregnant patient with normal anatomy most commonly have pain in acute appendicitis?

Correct answer: C

Rationale: In acute appendicitis, nonpregnant patients with normal anatomy commonly experience pain in the right lower quadrant of the abdomen. The pain usually starts around the umbilicus or epigastric area and then migrates to the right lower quadrant as inflammation progresses in the appendix. This classic migration of pain is known as McBurney's point tenderness and is a key clinical feature in diagnosing appendicitis.

5. What is the difference between alpha decay and beta decay?

Correct answer: B

Rationale: The correct answer is B. Alpha decay involves the release of a helium nucleus, which consists of two protons and two neutrons. In contrast, beta decay releases an electron (beta-minus decay) or a positron (beta-plus decay). This significant distinction in the particles emitted during the decay processes distinguishes alpha decay from beta decay. Choice A is incorrect because alpha and beta decay release different types of particles. Choice C is incorrect as beta decay is more common than alpha decay in many cases. Choice D is incorrect as it does not specifically address the particles released during alpha and beta decay.

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