arbon, as with many elements, can arrange its atoms into several different geometries, or "allotropes." In pure diamond, every carbon atom is covalently bonded to exactly 4 other carbon atoms in a very specific and energetically favorable geometry. The diamond cannot be broken or scratched unless many covalent bonds are broken, which is difficult to do. In another common allotrope, graphite, every carbon atom is covalently bonded to only 3 other carbon atoms, and the atoms are arranged in sheets that are not covalently bonded to each other. The sheets can be broken apart easily, ultimately meaning that graphite can be easily scratched. Coal is composed of particles of different allotropes of carbon, and some "amorphous carbon," which has no defined geometry in its atomic structure. Without a continuous network of covalent bonds, coal is easily scratched (i.e. it is not hard).
1) Pneumothorax in this case; a spontaneous pneumothorax can be life threatening cause the lung will eventually cause vacuum used by the lung to fill with air, and as you constantly expand your lung it decreases and collapses. So C is going to be the answer.
2) Acetylcholine is the hormone responsible for the "Rest and digest". It is the direct opposite of the Fight and Flight reaction which is marked in Bronchodilation, Increased HR, and increased BP. B
3) Secretin is responsible for stimulating the release of bile by the liver. Secretin is released by the duodenum, the junction of the stomach and small intestines. B
The correct answer is option A, that is, Phylum Porifera.
The species of Phylum Porifera are aquatic, that is, mostly marine. They exhibit cellular grade of the body, they are diploblastic animals with asymmetrical symmetry. They lack body cavity and exhibits a holozoic mode of nutrition with intracellular digestion.
They lack circulatory and nervous system and possess the tendency to regenerate their parts of the body. The organisms in phylum Porifera exhibits both asexual and sexual mode of reproduction.
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.
