Crossing over.
Yes, a karyotype is a display of an organism's chromosomes (generally in homologous pairs from largest to smallest).
True. The law of independent assortment, proposed by Gregor Mendel, states that genes for different traits segregate independently during the formation of gametes. This means that the inheritance of one trait generally does not influence the inheritance of another trait, assuming the genes are located on different chromosomes or are far apart on the same chromosome.
I don't have direct access to external websites like apex.com to verify specific statements. However, generally, the X chromosome is one of the two sex chromosomes in humans and many other organisms, playing a crucial role in determining sex and carrying genes related to various traits and conditions. If you have a specific statement or context in mind regarding X chromosomes, I can help clarify or discuss it!
When chromosomes line up this is generally part of mitosis or meiosis... the process of replicating or splitting and becoming gametes (sex cells).
The number of chromosomes in the cells of a potato root is also 24. Plant cells, including those in the root, generally have the same number of chromosomes as the parent plant.
When multiple sperm fertilize one egg, it results in an abnormal number of chromosomes, which can lead to a nonviable embryo. This phenomenon is known as triploidy and is generally not compatible with life.
Yes, a karyotype is a display of an organism's chromosomes (generally in homologous pairs from largest to smallest).
Organisms in the domain Eukarya have membrane-bound organelles, a nucleus, and multiple linear chromosomes, while organisms in the domain Archaea lack membrane-bound organelles, have a single circular chromosome, and their cell walls are chemically different. Eukaryotes generally have more complex cellular structures and processes than archaea.
Do you mean the similarities and differences between the new set of chromosomes and the parents' chromosomes? Or do you mean to ask about the comparison of the egg before/after fertilization?Only egg cells are fertilized.After fertilization, the egg should contain a complete set of chromosomes for the specific animal.If you meant the difference between the new set of chromosomes and the parents' individual chromosomes, the new set will generally contain the dominant genes of each gene type, and a few (generally minor) mutations. These mutations are what keep the organisms from slowly running out of non-relatives to breed with, in which case they would have had some severe genetic problems, as they would be amplified (which is the major problem of in-breeding).
possibly, different animals have different chromosome numbers, as do plants... so the chances are that yes there will be some plants that have the same amount of chromosomes as certain animals have... but they could never combine or cross with each other
well, "independent chromosomes" would be more like Anaphase I from meiosis; otherwise, it would be generally Anaphase. (it is not chromosomes but chromatids though, in mitotic anaphase.)
When chromosomes line up this is generally part of mitosis or meiosis... the process of replicating or splitting and becoming gametes (sex cells).
The number of chromosomes in the cells of a potato root is also 24. Plant cells, including those in the root, generally have the same number of chromosomes as the parent plant.
Termites typically have a diploid number of chromosomes that varies by species, but it generally ranges from 20 to 40 chromosomes. For example, the subterranean termite (Reticulitermes speratus) has 30 chromosomes. The specific number can differ significantly among the diverse species of termites.
no
A white blood cell generally contains 46 chromosomes, which is the normal number of chromosomes in a human cell. These chromosomes are arranged in 23 pairs, with one set of 23 chromosomes inherited from each parent.
The chromosomes, in their chromatin form generally, are located in the organelle called the nucleus.