Answer:
(<u>Bone deposition</u>),
<u>(Bone resorption</u><u>)</u>,
<u>Remodeling</u>
<u>Periosteal</u><u> </u>,
<u>Nedosteal,</u>
<u>The compact bone, </u>
<u> Spongy bone.</u>
Explanation:
The constant, dynamic process of continual addition of new bone tissue (<u>bone deposition</u>) and removal of old bone tissue (<u>bone resorption</u>) is a process called bone <u>remodeling</u>. This ongoing process occurs at both the <u>periosteal</u> (outer) and<u> nedosteal </u>(inner) surfaces of a bone.
It is estimated that about <u>nedosteal</u> of the adult human skeleton is replaced yearly. This process does not occur at the same rate everywhere in the skeleton. For example,<u> the compact bone</u> in our skeleton is replaced at a slower rate than the <u>spongy bone.</u>
The correct answer to this question is this one: "sporozoans lack locomotor organs"
The feature that differentiates sporozoans from the other phyla of protozoans is that sporozoans lack locomotor organs. Sporozoans are a strictly parasitic protozoan that are usually immobile.
Answer:
<h2>2. Peter's maternal grandfather has PKU.</h2>
Explanation:
- Such type of the genetic disorder in which two copies of a gene must be mutated at a time is called autosomal recessive disorder such as sickle cell anemia, phenylketonuria, and some other diseases.
- When a sing copy of a gene is mutated in a person then this disorder is not appeared and the person is called a carrier.
- So when a child is born by two carrier parents then there is a chance that a child will be affected if both the parents donate mutated genes.
- In the case of Peter, since peter does not show this defect this means his maternal grandfather was affected by this disorder.
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