The same way we never inject a full bag of anything quickly and intravenously. Your body would not be able to compensate for the amount of the substance. Alcohol or more importantly the Ethanol or Ethyl Alcohol in alcoholic beverages is the active ingredient of such beverages. It is also a drug called a CNS (Central Nervous System) depressant which means it is in the same class category of Opioids (Such as Heroin and Morphine) and Barbiturates (Rophynol). Your body processes alcohol via the liver, as it is also considered a toxin. By consuming a massive amount of alcohol without spacing it out, you will overload your system, not only literally overwhelming your liver and causing Alcohol Poisoning, but you also can go into a state similar to a Heroin overdose.
The right answer is pluripotent
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.
I believe it is a secondary consumer
The sequential order here is genetic information >> natural selection >> evolution. This order allowed the emergence of new adaptations (e.g., the gecko's coloration).
<h3>Natural selection</h3>
Natural selection is the main mechanism by which evolution occurs.
Evolution means descendence with modifications, it is a process that depends on the differential survival and reproduction of the most adapted individuals in a given environment.
Genetic information (variation) is a prerequisite for evolution to occur.
Learn more about natural selection here:
