CSHS 12 ATAR Biology chapter 2 quiz

CSHS 12 ATAR Biology chapter 2 quiz

12th Grade

50 Qs

quiz-placeholder

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CSHS 12 ATAR Biology chapter 2 quiz

CSHS 12 ATAR Biology chapter 2 quiz

Assessment

Quiz

Biology

12th Grade

Medium

NGSS
HS-LS3-2, HS-LS4-2, HS-LS3-1

+1

Standards-aligned

Created by

Mandy Webb

Used 7+ times

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50 questions

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1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

The variation seen in facial features of an Inuit person from Canada, a person from Japan and a person from Sweden are examples of:

biochemical variation.

behavioural variation.

intraspecific variation.

interspecific variation.

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which of the following best describes an allele?

A section of DNA found on a plasmid

A physical characteristic that is inherited

A combination of phenotypes

An alternative version of a gene

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which of the following contribute to genetic variation?

Crossing over and sexual reproduction

Asexual reproduction and mutations

Asexual reproduction and environmental change

Mitosis and random fertilisation

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Mutations are changes to DNA. A spontaneous mutation usually occurs:

in transcription.

when DNA is replicating.

in transcription or translation.

in reverse transcription.

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which of the following statements about mutations is true?

They are permanent changes in the DNA sequence.

They are mostly beneficial.

They can be caused by the individual’s environment.

The rate of mutations is influenced by the size of the genome.

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which of the following is probably not a mutagen?

(a mutagen is an agent that causes mutations)

Radiation, including X-rays

Cow’s milk

UV light

Benzene, an industrial solvent

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

The simplest form of mutation in DNA is a point mutation. Which of the following types of point mutation would have the greatest effect?

A point mutation in the non-coding region of a chromosome

A silent mutation

A missense mutation

A nonsense mutation

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