Answer:
Flatworms are beings that do not have a heart, veins, arteries, capillaries, hemolymph, or some type of circulatory fluid. Their circulation occurs between cells or intercellularly and they are responsible for transporting substances by diffusion from cell to cell.
Explanation:
Flatworms are considered multicellular eukaryotic organisms. This implies that in their cells they have a cellular nucleus, in which the DNA is contained, structuring the chromosomes. Likewise, they are made up of several types of cells, each one specialized in a specific function. They lack a structured circulatory system as such. Because of this they do not have specialized structures such as a heart or blood vessels, however, the circulation of certain substances is established between their cells. This is done thanks to the diffusion process. Substances pass from one cell to another through this process.This does not apply to all flatworms, since in some species of bog and digenae there is a certain organization and some very small conducting vessels known as the endolymphatic system, the which forms a kind of plexus in the parenchyma.It should also be noted that some species do not even have a digestive system, being the digestive tract the one in charge of digestive functions and the distribution of the nutrients they receive.
Lysosomes and chloroplasts are unique to plant cells.
ovary
These oocytes are formed during the early development of the person, it is together formed in the embryonic stage of development.
In puberty, these oocytes have now been mature thus, the individual is ready for her first menstruation, it takes time before these oocytes are fully developed but they are formed as early as the state of the genitalia, brain, body was formed.
<span>Somehow, it is like the brain, the brain is slowly developing til the near age of puberty or late childhood. </span>
<span>Eyes are also an analogy to oocytes, during infancy these organs aren't developed yet and these years the child can only see vague and blurred vision and takes almost 2 years for the child to see clearly.</span>
Answer:
If a female child has hemophilia it is possible that the mother is a carrier of the hemophilia gene and the father has hemophilia.
Explanation:
- A daughter gets X chromosome from both her parents.
- It is generally seen in males.
- Hemophilia is generally recessive in females.They act as carriers of hemophilia. This occurs because they have a X chromosome that dominates the hemophilia affected gene that they inherit from any parent.
- But, if both the parents have faulty genes ,i.e the mother is the carrier of the gene and the father is hemophiliac, then the chances are the daughter has hemophilia too.
Answer:
B. they bring cold , polar winds to the equator
