The chromosomal mutation in the zygote can be traced back to "Chromosome 6 in the egg cell".
<u>Option: B</u>
<u>Explanation:</u>
In germ cells i.e. egg or sperm cells, the mutations in chromosome often happen during the meiosis phase. The number of chromosomes in egg cells or sperm cells must be haploid, so that diploid chromosomes form zygote on fertilization. Chromosome mutation in meiosis leads in an additional set of chromosomes or structural defects in the chromosome.
Chromosomal mutations are often caused by chemical agents or by mutagens.
The homologous chromosomes are segregated from sister chromatids throughout cell division, any abnormality at this point allows the chromosomes to be unequally divided or not disjuncted, same is observed in the situation seen in egg cell chromosome 6.
I would say all of the above
Is that an option?
Answer:
1) the genes and chromosomes do not double after each generations because parental sex cells are haploid and only contain one set of chromosomes. During fertilization the two cells fuse to form a diploid zygote with two copies of genes and chromosomes. For example a normal human has 46 chromosomes (2 copies of 23 chromosomes) during reproduction gametes which contain 23 chromosomes (haploid) fuse to form an offspring with the correct number of chromosomes ( 23 + 23 = 46).
2) offspring only receive one set of chromosomes from each parent so to maintain the chromosome number of humans. If this did not happen you would not be the same species.
Answer:
The most common elements, like carbon and nitrogen, are created in the cores of most stars, fused from lighter elements like hydrogen and helium. The heaviest elements, like iron, however, are only formed in the massive stars which end their lives in supernova explosions.
Explanation:
