The amount of plants in the region would grow, but the amount of carnivores who eat the herbivores would diminish.
Correct question:
if a nondisjunction occurs at anaphase I of the first meiotic division, what will the proportion of abnormal gametes (for the chromosomes involved in the nondisjunction)?
Answer:
100%
Explanation:
Nondisjunction at meiosis-I means that two homologous chromosomes of at least one homologous pair fail to separate from each other during anaphase-I. This would result in the formation of one cell with one extra chromosome and the other with one less chromosome by the end of meiosis-I. Meiosis-II in these two cells would maintain this chromosome number in the daughter cells. Therefore, out of the total four gametes formed by the end of the meiosis, two would have one extra chromosome and would be denoted as "n+1". The rest of the two gametes would have one less chromosome and would be denoted as "n-1".
the answer is yess hope it is
Answer:
Regions of the digestive system can be divided into two main parts: the alimentary tract and accessory organs.
the alimentary tract and accessory organs.
Explanation:
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1. The answer is Telophase.
This is the last step of mitosis, during which the sister chromatids reach opposite poles. The small nuclear vesicles in the cell begin t reform around the group of chromosomes at each poles. Mitosis is a very important part of cell division because it is the process by which the parent cell gives its DNA to its two daughter cells.
2. The correct answer is 4. The cell would not be able to grow any further
Body cells divide by the process of mitosis; a process in which a body cells undergoes division tow yield two diploid daughter cells, the process enhances growth and development as the cell increase in number by multiplying themselves.
3. The correct answer Telophase II;
In prophase II, the nuclear envelop breaks down the spindle apparatus forms. The nuclear envelope forms around each set of chromosomes and cytokinesis occurs, producing four daughter cells, each with haploid set of chromosomes.
4. The answer is 4. its body cells would have 36 chromosomes and its gametes would have 18 chromosomes. The somatic cells or the body cells are cells that have diploid (two pairs of chromosome) number, while the gametes are formed from the process of meiosis and contains haploid number of chromosomes.
5. The best answer is ; meiosis ; it increases genetic variation, which helps ensure the species will survive. Meiosis is a type of cell division in which a cell (germ-line cells), where a cell divides to yield four daughter cells which are haploid; Meaning they have half the number of chromosomes as the parent cell.
6. The answer is 50 percent. If the dominant allele is Y and the recessive allele; Therefore; the heterozygous will be Yy and the homozygous green color will be yy.
Thus; A cross between heterozygous Yy and the green recessive yy will yield; 50 percent heterozygous and also half homozygous recessive.
7. The correct answer is that One parent was heterozygous for eye color and the other was homozygous with red eyes.
An organism can be homozygous dominant, if it carries two copies of the same dominant allele, or homozygous recessive, if it carries two copies of the same recessive allele. Heterozygous on the other hand, means that the organisms has two different alleles of a gene.
8. The correct answer is that the children will all have type AB blood. Both A and B alleles are dominant over O. as a result, individuals who have an AO genotype will have an A phenotype. The A and B alleles are codominant. When two alleles for a trait are equally expressed with neither being recessive or dominant, it creates codominance.
9. I believe the disease inheritance pattern described above by the cart shows Sex linked recessive inheritance pattern and in a cross between two heterozygous individuals there is a 50 percent chance for the second child born to be affected.
10. The answer for the question is 50 % percent.
I think that the infection design that is described above is a sex linked recessive legacy design and in a cross between two heterozygous individuals, there will be a half or 50 percent probability or possibility for the second child to be influenced.
