<span>they both have two alleles
</span>they both express the dominant allele (aka the phenotype or physical traits of the allele). They are different in genotype though, which is their genetic make up because homozygous would be two dominant alleles and heterozygous is a combination of dominant and recessive allele. Homozygous recessive and heterozygous are completely different <span>though in genotype and phenotype.</span>
Answer:
Heterozygous
Explanation:
A genotype describes which alleles of a particular gene a person has. We have two copies (alleles) of each gene, one from mom and one from dad, but these alleles can be different.
Often, these alleles can be dominant and recessive with regards to eachother. The dominant allele will always be displayed in the phenotype, whereas the recessive will not be presented, as it is masked by the dominant gene. If you have two copies of the dominant gene (homozygous) you will display the phenotype associated with the dominant genotype. If you have two copies of the recessive gene (homozygous) you will display the phenotype of the recessive gene.
If you have one copy of each (heterozygous), you will display the phenotype of the dominant gene, even though your genotype has a copy of each.
The Burgess Shale is a rock formation that is known for having an abundance of soft bodied organisms preserved in shale. This formation is significant because it preserves organisms from the Cambrian Explosion. The Cambrian Explosion is a period in time that coincides with the Pre- Cambrian- Cambrian boundary around 542 million years ago. The period represents an unusually rapid radiation of organisms.
Fossils of the Burgess Shale are thought to be well preserved because most were thought to be buried fairly rapidly and in conditions that had little or no oxygen. The rate of decomposition is slowed in these conditions so soft body parts of the organisms were preserved for millions of years in the mud-stone that eventually became lithified to shale. <span />
Answer: Meiosis; fertilization
In the human life cycle, diploid cells undergo a cell division process called meiosis. The resulting haploid cells later fuse during fertilization which regenerates diploid cells.
Explanation:
Diploid cells possess two basic sets of chromosomes known as homologous chromosomes. They undergo a two-step meiosis (Meiosis I and II) to yield four haploid cells with half the original chromosome number of the parent cell. These haploid cells are called sex cells or gametes.
The male and female gametes (sperm and egg) then fuses during fertilization to form zygote, a single cell with two sets of chromosomes (diploid number). Then, it undergoes mitosis to regenerates diploid cells with the same chromosome number as found in the zygote.
the intellectual and practical activity encompassing the systematic study of the structure and behavior of the physical and natural world through observation and experiment.