<h2>B) option is correct </h2>
Explanation:
Natural selection is a selection pressure which operates in a population and allow the best fitted genotype to survive in changing environmental conditions and eliminate the other genotype which are not fit
In artificial selection, breeders select superior breed for the breeding purpose so that this type of selection favors the superior genotype and eliminates inferior genotype, thus leading to genetic drift
Stabilizing selection is a type of natural selection in which intermediate genotype is favored but extreme genotypes (inferior and superior) are eliminated
In the given example of pigmentation in pigeons, breeding is selectively done with intermediate pigmentation hence intermediate genotypes will be favored
Answer:
the answer to this question is choice D
D. strings because if you have a ¨concert band¨ with strings in it then it is called an orchestra.
Answer:
UUAGUACCU
Explanation:
A ---> U
T ---> A
C ---> G
it's been a while since I did this stuff but I'm 99% sure it's correct
Answer:
- Calcium binds to troponin C
- Troponin T moves tropomyosin and unblocks the binding sites
- Myosin heads join to the actin forming cross-bridges
- ATP turns into ADP and inorganic phosphate and releases energy
- The energy is used to impulse myofilaments slide producing a power stroke
- ADP is released and a new ATP joins the myosin heads and breaks the bindings to the actin filament
- ATP splits into ADP and phosphate, and the energy produced is accumulated in the myosin heads, starting a new cycle
- Z-bands are pulled toward each other, shortening the sarcomere and the I-band, producing muscle fiber contraction.
Explanation:
In rest, the tropomyosin inhibits the attraction strengths between myosin and actin filaments. Contraction initiates when an action potential depolarizes the inner portion of the muscle fiber. Calcium channels activate in the T tubules membrane, releasing <u>calcium into the sarcolemma.</u> At this point, tropomyosin is obstructing binding sites for myosin on the thin filament. When calcium binds to troponin C, troponin T alters the tropomyosin position by moving it and unblocking the binding sites. Myosin heads join to the uncovered actin-binding points forming cross-bridges, and while doing so, ATP turns into ADP and inorganic phosphate, which is released. Myofilaments slide impulsed by chemical energy collected in myosin heads, producing a power stroke. The power stroke initiates when the myosin cross-bridge binds to actin. As they slide, ADP molecules are released. A new ATP links to myosin heads and breaks the bindings to the actin filament. Then ATP splits into ADP and phosphate, and the energy produced is accumulated in the myosin heads, which starts a new binding cycle to actin. Finally, Z-bands are pulled toward each other, shortening the sarcomere and the I-band, producing muscle fiber contraction.
