I THINK humid but I'm not completely sure
Answer:
D. is caused by alcohol consumption
Explanation:
- ADH hormone is also called as vasopressin, it is secreted by the supraoptic nuclei of hypothalamus and released by posterior pituitary.
- The main function of ADH is to stimulate reabsorption of water from kidney tubules i.e DCT (distal convoluted tubules) and collecting duct.
- Anti diuretic means against diuresis (excess urination or loss of water). Insufficient ADH can lead to diabetes insipidus which includes the symptoms such as diuresis and dehydration but no glucose in urine.
- Alcohol suppresses the release of ADH, thus water reabsorption reduces and urine volume increases.
- Very high levels of ADH can result in dangerous conditions such as cerebral edema due to excess fluid buildup in the body.
- ADH allows the kidney to form concentrated urine while excreting normal amounts of salts. Continuous secretion of ADH may lead to hyponatremia i.e decrease of sodium levels in blood.
- Angiotensin II is released when there is low BP and it stimulates release of vasopressin/ADH to cause the vaso-constriction, there by bring the BP to normal.
The part of the Sun that you are observing when you see a blotchy appearance is the surface of the sun. This appearance is called granulation which is caused by the convection of the hot material inside the sun which go up and down the surface of the sun. Because of its sandy texture it is sometimes called lemon peel or rice grain.
It represents the split chromosome is true about the chromatids.
<h3>What are the chromatid's characteristics?</h3>
One of a chromosome's two identical halves that has undergone replication in order to facilitate cell division is referred to as a chromatid. The centromere, a constrictive area of the chromosome, serves as the connection between the two "sister" chromatids.
<h3>What is a chromatid's purpose?</h3>
It permits cells to store two copies of their info in order to get ready for cell division. This is crucial to ensuring that daughter cells are strong and completely functional, carrying the entire complement of DNA from the parent cells.
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A mutation within a gene that will insert a untimely cease codon in mRNA would result in a shortened polypeptide chain.
<h3>What occurs if there is a untimely end codon?</h3>
Thus, nonsense mutations occur when a premature nonsense or end codon is added in the DNA sequence. When the mutated sequence is translated into a protein, the resulting protein is incomplete and shorter than normal. Consequently, most nonsense mutations result in nonfunctional proteins
<h3>What mutation motives untimely cease codon?</h3>
In genetics, a nonsense mutation is a factor mutation in a sequence of DNA that effects in a premature stop codon, or a nonsense codon in the transcribed mRNA, and in a truncated, incomplete, and normally nonfunctional protein product.
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