Answer:
meiosis
Explanation:
Mitosis creates two identical daughter cells that each contain the same number of chromosomes as their parent cell. In contrast, meiosis gives rise to four unique daughter cells, each of which has half the number of chromosomes as the parent cell.
The genetic fault that usually causes colour vision deficiency is passed on in what's known as an X-linked inheritance pattern.
This means:
1) it mainly affects boys, but can affect girls in some cases
2) girls are usually carriers of the genetic fault – this means they can pass it on to their children, but do not have a colour vision deficiency themselves
3) it's usually passed on by a mother to her son – the mother will often be unaffected as she'll normally just be a carrier of the genetic fault
4) fathers with a colour vision deficiency will not have children with the problem unless their partner is a carrier of the genetic fault
5) it can often skip a generation – for example, it may affect a grandfather and their grandson
6) girls are only affected if their father has a colour vision deficiency and their mother is a carrier of the genetic fault
It could be a common ancestry among organisms.
Human and the natural ones can change the ecosystem