Answer:
Personally, I believe the information helps.
Explanation:
Without this information the virus would not be contained, we would not have done research, taken samples, tested out the virus, or even attempted to contain it. With this information we can attempt to prevent a break out of the disease again. This is my personal opinion though.
<em><u>T</u></em><em><u>h</u></em><em><u>e</u></em><em><u> </u></em><em><u>mutation</u></em><em><u> </u></em><em><u>Mutations are changes to an organism's DNA and are an important driver of diversity in</u><u> </u><u>populations.</u><u> </u><u>This mutation has introduce a new allele into the population that increases genetic variation and may be passed on to the next generation.</u></em>
<em><u>hope</u></em><em><u> </u></em><em><u>it</u></em><em><u> </u></em><em><u>helps</u></em><em><u>.</u></em>
Answer:
<em>B. Different crops could be grown on the same land.
</em>
Explanation:
Crop rotation is the process of growing different plants in the same land according to the season. Various kinds of plants require various sorts of supplements from the soil.
Changing crops on a regular basis enables the land to stay rich in nutrients, since not the majority of similar nutrients are being utilized each season. Crop rotation likewise fights against the powers of soil erosion. It also helps to improve the stability of the soil by shifting back and forth between harvests with profound roots and those with shallow roots.
Answer:
At the beginning you start out with a lot of energy and stamina but as you progress, maybe five minutes in, you start to get out of breath. While breathing harder, you are trying to intake more oxygen and at the 10 minute mark you can feel your muscles burning a little bit and tire out more. At this point you are gasping for oxygen because your muscles are deprived of oxygen and you body makes lactic acids which you muscles can use instead of oxygen. By the end of it you are very tired.
Explanation:
Hope this helps! I am not sure how scientific of an explanation you wanted.
<span>There are numerous proteins in muscle. The main two are thin actin filaments and thick myosin filaments. Thin filaments form a scaffold that thick filaments crawl up. There are many regulatory proteins such as troponin I, troponin C, and tropomyosin. There are also proteins that stabilize the cells and anchor the filaments to other cellular structures. A prime example of this is dystrophin. This protein is thought to stabilize the cell membrane during contraction and prevent it from breaking. Those who lack completely lack dystrophin have a disorder known as Duchene muscular dystrophy. This disease is characterized by muscle wasting begininng in at a young age and usually results in death by the mid 20s. The sarcomere is the repeating unit of skeletal muscle.
Muscle cells contract by interactions of myosin heads on thick filament with actin monomers on thin filament. The myosin heads bind tightly to actin monomers until ATP binds to the myosin. This causes the release of the myosin head, which subsequently swings foward and associates with an actin monomer further up the thin filament. Hydrolysis and of ATP and the release of ADP and a phosphate allows the mysosin head to pull the thick filament up the thin filament. There are roughly 500 myosin heads on each thick filament and when they repeatedly move up the thin filament, the muscle contracts. There are many regulatory proteins of this contraction. For example, troponin I, troponin C, and tropomyosin form a regulatory switch that blocks myosin heads from binding to actin monomers until a nerve impulse stimulates an influx of calcium. This causes the switch to allow the myosin to bind to the actin and allows the muscle to contract. </span><span>
</span>