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iogann1982 [59]
3 years ago
7

What is land pollution?

Biology
1 answer:
Gwar [14]3 years ago
3 0
When people throw their garbage on the ground
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The <br> layer of the skin is made of dead cells.
Harrizon [31]

Explanation:

The stratum corneum, which is the outermost epidermal layer, consists of dead cells

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3 years ago
Predict phenotypes associated with nondisjunction of sex chromosomes.
Mnenie [13.5K]

Answer: The new daughter cells will have an abnormal amount of genetic material. That is called aneuploidy and it is the presence of an abnormal number of chromosomes. Different clinical conditions are the result of this nondisjunction.

Explanation:

Normal cells are diploids, that means they have two copies of each gene, one of each chromosome. So normal cells have two homologous chromosomes, one from each parent.

During anaphase of cell division, each pair of chromosomes is separated  by the mitotic spindle. The separated chromosomes are then pulled by the spindle to opposite poles of the cell, and eventually will end up in the new daughter cells.

Nondisjunction is the failure of homologous chromosomes to separate properly during cell division, so it is the miss segregation of them. The new daughter cells will have an abnormal amount of genetic material. <u>Different clinical conditions are the result of this nondisjunction.</u>

Sex chromosomes participates in sex determination of an individual. Females have two X chromosomes (XX), while males have one X and one Y chromosome (XY) So nondisjunction of sex chromosomes could be:

  • XX: one cell with no chromosome and the other cell with two X chromosomes.
  • XY: one cell with no chromosomes and the other cell with XY chromosomes.

According to which gametes are fused during fertilization, different phenotypes can be given. For example, if a gamete with one chromosome fuses with another gamete with two chromosomes, the result will be an individual with three chromosomes (it could be XXY, or XXX) called trisomy.

Triple X syndrome is characterized by an extra X chromosome in females. Those affected are often taller than average, but most females have a normal sexual development. Klinefelter syndrome is known XXY individuals, and it causes infertility in males, breast growth, less body hair and weaker muscles.

And if a gamete with no chromosome fuses also with another gamete with no chromosome, the result is a nullisomy. But due to the lack of genetic material, the nullisomic gametes are rendered unviable for fertilization.

And if a gamete with no chromosome fuses with another gamete with one chromosome (normal) the result is a monosomy, the presence of only one chromosome from a pair. The result can be an individual who is X or Y. People with Turner syndrome have one X chromosome and it is the only monosomy that is seen in humans because other cases monosomy are lethal.

Any of those examples is called aneuploidy and it is the presence of an abnormal number of chromosomes.

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3 years ago
New Zella article called: how chromosome mutations occur. There are four questions on the quiz I can't get any of them. Please h
nadezda [96]

Answer:

Change in the structure of chromosome.

Explanation:

Chromosome structure mutations are the changes that occur in the structure of chromosomes rather than just individual nucleotides. These mutations occurs due to the errors that happens in cell division that leads to the breaking in section of a chromosome, which can be duplicated or move onto another chromosome. Chromosome mutation is the process of change in the chromosomes that occurs due to the rearranged chromosome parts and  abnormal numbers of individual chromosomes.

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The genetic makeup of an individual is called the what phenotype genotype DNA structure characteristics
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Genotype . ...........
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Algae is more simple than plants
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