Is it due to attachement of bronken part of one chromosome to another. I hope this helps.
Answer:
The correct answer would be
- Concave lens for nearsightedness
- Convex lens for farsightedness
Nearsightedness or myopia is a condition in which a person can see the nearby objects clearly but is unable to see the objects present at a farther distance clearly.
It is usually caused due to elongation of the eyeball or when the lens becomes too curved.
It can be corrected by using a concave or diverging lens of appropriate power.
Farsightedness or hyperopia is a condition in which a person can see the distant objects clearly but is unable to see the nearby objects distance clearly.
It is usually caused due to shortening of the eyeball or when the lens loses its curvature.
It can be corrected by using a convex or converging lens of appropriate power.
Answer:
The correct answer is option E.
Explanation:
The deep-colored, water-soluble proteins, which are mainly found in Rhodophyta and cyanobacteria are known as phycobiliproteins. They captivate the light energy and then pass it to the chlorophyll at the time of photosynthesis.
They are comprised of proteins and are covalently attached through cysteine amino acid chromophores known as phycobilins. Thus, the correct answer is option E.
Hey!
The correct answers for the blanks that I can answer (as a third-person answerer) are as follows:
*No, some collisions do not cause reactions due to a lack of energy or ability to properly collide.
*Speed
*A change in temperature of the bicarbonate reaction may lead to a quicker reaction with CO2-producing molecules.
I hope I helped!
Feel free to leave a comment down below if you need any more assistance or if I skipped any sections of the prompt. I will gladly help you with anything! :)
Answer:
Explanation:
If the disorder is recessive, neither parent has to have the disorder because
they can be heterozygous. The characteristic features of autosomal recessive inheritance is as follows:-
•Appears in both sexes with equal frequency
• Trait tend to skip generations
• Affected offspring are usually born to unaffected parents
• When both parents are heterozygous approx. 1/4 of the progeny will be affected
• Appears more frequently among the children of consanguineous marriages.
The given pedigree follows these features. So the correct option is 'Autosomal recessive trait'.
Please correct me If I am wrong :)
