Answer:
The hard parts of organisms, such as bones, shells, and teeth have a better chance of becoming fossils than do softer parts. One reason for this is that scavengers generally do not eat these parts. Hard parts also decay more slowly than soft parts, giving more time for them to be buried.
Explanation:
Answer:
★ A nonrenewable resource that developed from the remains of ancient plants that lived in large swamps millions of years ago is COAL
Explanation:
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Answer:
The correct answer would be:
- Genotype ratio: 1 (PP) : 2 (Pp) : 1 (pp)
- Phenotypic ratio: 3 (polka-dot tails) : solid colored tail
The genotype of both parents is Pp (heterozygous).
Thus, both the parent would produce two types of gametes which are P and p.
The cross would result in the production of offspring with three types of genotype PP, Pp, and pp in 1:2:1.
Offspring with PP and Pp will have a polka-dotted tail as it is the dominant trait.
Thus, the phenotype ratio would be 3 (polka-dotted tail) : 1 (solid colored tail).
The question is incomplete. The complete question is as follows:
Which of the following mutations is most likely to cause a phenotypic change?
A) a duplication of all or most introns
B) a large inversion whose ends are each in intergenic regions
C) a nucleotide substitution in an exon coding for a transmembrane domain
D) a single nucleotide deletion in an exon coding for an active site
E) a frameshift mutation one codon away from the 3' end of the nontemplate strand
Answer: D) a single nucleotide deletion in an exon coding for an active site
Explanation:
Deletion or insertion of a single nucleotide in an axon coding for an active site is called frameshift mutation.
The sequence of codons is read during translation, in order to synthesize a amino acids chain and form a protein from the nucleotide sequence. Frameshift mutations occur when the usual codon sequence is broken by the deletion or addition of one or more nucleotides. For example, if only one nucleotide is removed from the axon sequence during the RNA splicing process, then there will be a disrupted reading frame for all codons before and after the mutation. This may result in several incorrect amino acids being introduced into the protein. Disruption in protein sequence will cause phenotypic change.
Hence, the correct option is D) a single nucleotide deletion in an exon coding for an active site
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