Answer:
true
Explanation:
binary fission, in biology, is the division of a single entity into two or more parts and the regeneration of those parts to separate entities resembling the
Answer: Structural chromosomal mutation
Explanation: In translocation, a small piece of chromosome is detached from one chromosome and is attached to another non-homologous chromosome. Translocation can be simple, shift or reciprocal.
Simple translocation involves single break in the chromosome. The broken piece gets attached to the end of the non-homologous chromosome.
In Shift translocation, the broken segment of one chromosome gets inserted interstitially in a non-homologous chromosome.
Segment from one chromosome is exchanged with a segment from another non-homologous chromosome simultaneously in Reciprocal translocation.
Answer is C bc of the fact of diameter
F1 stands for first filial (daughter) generation
<span>F2 stands for second filial (daughter) generation</span>
As we can see in the pedigree, both of the parents do not possess the trait, but one of the four offspring (marked with red) is expressing the trait.
Since the trait is recessive, the only way that is possible that the parents who do not possess the trait to have the offspring with the trait is that the parents are heterozygous for the trait. Meaning that both of the parents have one dominant allele and one recessive allele.