Answer:
where the is the picture?
Your answers would be:
1. ---- B. A cell cannot be subdivided into smaller units that maintain the living state.
2. ---- The organism is a eukaryote because it has a nucleus.
3. ---- D. Water would flow into them because they are hypertonic to external environment.
If you want to know why:
1. The cell is the basic unit of life or in other words, its the smallest unit that makes up a living thing. It does not subdivided further if you are talking about sustaining life. Yes, it is made up of smaller units of organelles, but these organelles work together as a single unit (as a cell), to do life sustaining processes.
2. The organism is a eukaryote because of the presence of a nucleus. This is one of the main features of a eukaryote that differentiates it from a prokaryote. Prokaryotes to not have a true nucleus.
3. Water would flow into them, causing the cell to swell and eventually burst if the concentration of solutes would not even out before then. The process of osmosis is what brings the water into the cell. The cell would have a higher solute concentration than freshwater. Through osmosis, the water would then go to the area of higher concentration, which would be the cell.
Answer:
Waning is the opposite, or decreasing after a full moon, and is always illuminated on the left. Then, there is a waxing or waning Gibbous moon, which means more than half of the moon is illuminated. Waxing means to increase/get bigger, and waning means to decrease/get smaller.
Answer:
B. The father did not contribute a sex chromosome to his daughter due to nondisjunction of the sex chromosomes. The daughter is XO and her only X chromosome came from her mother, who was a carrier.
A.The mother's X chromosomes failed to separate during meiosis, and the daughter inherited two X chromosomes with the Lesch-Nyhan mutation. The father contributed no sex chromosomes.
Explanation:
As seen in the question above, a little girl was diagnosed with Lesch-Nyhan syndrome, which is an X-linked recessive condition caused by a mutation in the HPRT1 gene responsible for purine metabolism.
The little girl's parents do not have the syndrome, and no one in the little girl's paternal family presented this syndrome, however, we know that the maternal grandfather of the little girl's mother had the syndrome, which means that it was the mother's genetic material that contributed to the development of the syndrome in the little girl. This was because the little girl did not receive any X chromosomes from her father, but she inherited the two X chromosomes from her mother that coded for the Lesch-Nyhan mutation. This happened because the mother's X chromosome disjuction did not occur during meiosis I.
As shown above, the father did not contribute any sex chromosomes to his daughter, which means that the daughter is XO and her only X chromosome came from her mother, who was a carrier.
These reactions are METABOLISM.
