Nursing Elites

1. Delta waves, associated with deep sleep, exhibit what frequency range?

• A. 0.5-4 Hz
• B. 4-8 Hz
• C. 8-13 Hz
• D. 13-30 Hz

Correct answer: A

Rationale: Delta waves are slow brain waves associated with deep sleep stages, specifically stages 3 and 4 of non-REM sleep. These waves have a frequency range of 0.5-4 Hz. Choice B (4-8 Hz) refers to theta waves, which are associated with light sleep and relaxation. Choice C (8-13 Hz) corresponds to alpha waves, present during wakeful relaxation. Choice D (13-30 Hz) represents beta waves, seen in active thinking and concentration. Therefore, the correct answer is A because it aligns with the frequency range characteristic of delta waves during deep sleep.

2. Which layer of the skin is responsible for new skin cell production?

• A. Stratum corneum
• B. Stratum basale
• C. Stratum granulosum
• D. Stratum spinosum

Correct answer: B

Rationale: The correct answer is B, Stratum basale. The stratum basale, also known as the basal layer or stratum germinativum, is the deepest layer of the epidermis and is responsible for new skin cell production through cell division. It contains basal cells that continuously divide to produce new keratinocytes, which move up through the layers of the epidermis. Choice A, Stratum corneum, is the outermost layer of the epidermis consisting of dead cells filled with keratin. It serves a protective function but is not involved in new skin cell production. Choice C, Stratum granulosum, is a layer of the epidermis where keratinocytes undergo changes in their structure and composition. It is involved in the process of keratinization but not in new skin cell production. Choice D, Stratum spinosum, is a layer of the epidermis where cells become interconnected by desmosomes. While it plays a role in providing strength and support to the epidermis, it is not primarily responsible for new skin cell production.

3. With which genotype would the recessive phenotype appear if the dominant allele is marked with 'A' and the recessive allele is marked with 'a'?

• A. AA
• B. aa
• C. Aa
• D. aA

Correct answer: B

Rationale: The recessive phenotype appears when an individual has two copies of the recessive allele. In this case, the recessive allele is marked with 'a.' Therefore, the genotype 'aa' would display the recessive phenotype as both alleles are recessive. Choice A (AA) has two dominant alleles, choice C (Aa) has one dominant and one recessive allele, and choice D (aA) represents the same genotype as Aa due to the principle of allele dominance.

4. What is the primary function of the respiratory system?

• A. Maintain body temperature
• B. Deliver oxygen to the bloodstream and remove carbon dioxide
• C. Produce antibodies for the immune system
• D. Break down food molecules for energy

Correct answer: B

Rationale: The primary function of the respiratory system is to deliver oxygen to the bloodstream and remove carbon dioxide. This process occurs through breathing, where oxygen is inhaled into the lungs and then transferred to the bloodstream, while carbon dioxide is removed from the bloodstream and exhaled out of the body. Maintaining body temperature (A), producing antibodies for the immune system (C), and breaking down food molecules for energy (D) are functions of other systems in the body, not the respiratory system. Therefore, the correct answer is B.

5. Which type of mutation involves a change in the number of chromosomes?

• A. Point mutation
• B. Frameshift mutation
• C. Missense mutation
• D. Aneuploidy

Correct answer: D

Rationale: A) Point mutation involves a change in a single nucleotide base pair within the DNA sequence. B) Frameshift mutation involves the insertion or deletion of nucleotides, causing a shift in the reading frame of the genetic code. C) Missense mutation involves a single nucleotide change that results in a codon that codes for a different amino acid. D) Aneuploidy involves a change in the number of chromosomes, where an individual may have an extra chromosome (trisomy) or a missing chromosome (monosomy). Aneuploidy can lead to genetic disorders such as Down syndrome (trisomy 21) or Turner syndrome (monosomy X). Changing the number of chromosomes is a characteristic feature of aneuploidy, making it the correct answer. Point mutation, frameshift mutation, and missense mutation do not involve a change in the number of chromosomes and are focused on alterations at the nucleotide level within the DNA sequence.

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