Answer: All of the rock in the Earth is recycled and accounted for during the rock cycle. This principle applies to other areas of science as well and is known as conservation of mass, which says that mass cannot be created or destroyed but is cycled between different forms.
Explanation:
Tissues are below complex organs.
<h3>What are the tissues?</h3>
- The body is made up of four different types of tissue: epithelial, connective, muscular, and nervous. Each has a purpose for which it was created.
- Connective tissue, epithelial tissue, muscular tissue, and nerve tissue are the four fundamental forms of tissue. Other tissues are held together and supported by connective tissue (bone, blood, and lymph tissues). A coating is provided by epithelial tissue (skin, the linings of the various passages inside the body).
- Tissue that gives bones their strength and structure. Compact tissue (the tough outer layer) and cancellous tissue make up bone (the spongy, inner layer that contains red marrow). Osteoblasts, which build new bone, and osteoclasts, which break down existing bone, maintain bone tissue.
- Blood tissues can be found inside blood vessels, including arteries, arterioles, capillaries, venules, and veins (for more information on the names of individual blood vessels and the course the blood takes, see systemic circulation), as well as inside the heart's chambers.
To find the level is just below organs in complexity:
Tissues are below complex organs.
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Answer:
Explanation:
Galactosemia is an inherited metabolic disorder caused by changes, or mutations, in both copies of an individual’s GALT gene. In the majority of cases, children with galactosemia do not have parents with galactosemia. Mother and father separately are a silent carrier of the condition, which is expressed in the child (autosomal recessive inheritance).
Each individual has two copies of the GALT gene – one from father and one from mother. In case of any changes of these genes (mutations) that prevents the gene from working correctly. In order to inherit galactosemia, it is necessary for a child to have two GALT gene changes. In case of one GALT gene change there is no galactosemia.
Infants with galactosemia may be identified through newborn screening programs or by symptoms that present during the first few weeks of life. Untreated infants develop liver and kidney disease, cataracts in their eyes, and serious infections.
the answer you are looking for is B. Glucose is broken down into two pyruvate molecules.
this process occurs during glycolysis
