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Ann
2 months ago
14

There are 100,000 students, staff, and faculty with an account at ASU, and when the virus was discovered, there were already 100

0 accounts infected and 2000 account recovered from the virus. We can formulate the problem as a standard SIR model. The model has a time step size of one hour. From the data of the first hours of the virus spreading through the system we know that α is 0.00001 and that it takes half a day for a computer to be recovered (the average time it takes for people to upload and execute a virus destruction program). a: What is the value of R0?
Biology
1 answer:
vlada-n [2.5K]2 months ago
8 0

Answer:

The body combats the virus, and upon its return, it can recognize and eliminate it. However, during this process, we rely on antibodies and other mechanisms to fight off the virus, which explains the weakness felt in that period. It may take time to completely eradicate the virus.

This explains the conclusion.

Explanation:

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In his study of pea plants, Gregor Mendel used which method to produce offspring?
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The method is cross-pollination, achieved by utilizing parents with distinct traits.

Gregor Mendel studied pea plants and formulated the foundational principles of heredity. He coined the terms dominant and recessive to describe traits, based on his experiments. He practiced cross-pollination, which involves mating parents that exhibit different traits. For instance, he crossed a plant bearing green peas with another showcasing yellow peas (two contrasting traits) and examined the inheritance of these traits in subsequent generations.
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The narrow, elongated, hollow cells that make up xylem tissue of plants allow for A. the production of glucose by photosynthesis
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The answer is; D


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2 months ago
Using the sliding flament theory, explain (or draw) the process of sarcomere shortening. Start from the point where calcium woul
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Answer:

  1. Calcium attaches to troponin C
  2. Troponin T shifts tropomyosin to reveal the binding sites
  3. Myosin heads connect to actin, forming cross-bridges
  4. ATP is converted to ADP and inorganic phosphate and releases energy
  5. This energy drives the sliding of myofilaments, resulting in a power stroke
  6. ADP detaches and a fresh ATP binds to the myosin heads, breaking the bond with the actin filament
  7. ATP is then split into ADP and phosphate, storing energy in the myosin heads, thus beginning another cycle
  8. Z-bands are drawn together, which shortens the sarcomere and the I-band, leading to muscle contraction.

Explanation:  

At rest, tropomyosin blocks the attraction between actin and myosin filaments. Contraction starts when an action potential depolarizes the interior of the muscle fiber. Calcium channels in the T tubules open, leading to the release of calcium into the sarcolemma. At this moment, tropomyosin obstructs the myosin binding sites on actin. Upon binding of calcium to troponin C, troponin T modifies the position of tropomyosin, exposing the binding sites. Myosin heads attach to the exposed actin sites forming cross-bridges, while ATP is converted into ADP and inorganic phosphate, which is then released. The sliding of myofilaments is driven by the chemical energy stored in myosin heads, resulting in a power stroke. The power stroke starts as the myosin cross-bridge binds to actin. During the slide, ADP is released. A new ATP connects to myosin heads, terminating the bond with the actin filament.  Then ATP is split into ADP and phosphate, and the energy generated is stored in the myosin heads, which initiates a new cycle of binding to actin. In the end, Z-bands pull together, which shortens the sarcomere and the I-band, causing muscle fiber contracture.

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Explanation:

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