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meriva
3 years ago
13

Why is water displacement an effective way of measuring the volume of an irregular solid?

Biology
2 answers:
HACTEHA [7]3 years ago
5 0
The answer your looking for is A
Nutka1998 [239]3 years ago
4 0

Answer: Option (B) is the correct answer.

Explanation:

We cannot find the volume of an irregular solid because we can never measure the volume of curves that are present in an irregularly shaped object.

Therefore, we tend to place this irregular object in a beaker of water so that the volume of water displaced by it will actually show us the volume of object itself.

Hence, we can conclude that water displacement is an effective way of measuring the volume of an irregular solid there is no way of finding the volume of an irregular shape.

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Amoeba Sisters Video Recap: DNA Replication
Sergio039 [100]

Before starting the explanation in the amoeba sister video, they explain what DNA replication is. We can say that DNA, which in eukaryotic cells is located in the nucleus, contains all the genetic information of a being and its duplication process is important for cell growth, reproduction and repair.

<h3 /><h3>What is DNA replication?</h3>

A DNA molecule is made up of two strands that complement each other. For example, if we have an F and an F' strand, in the replication process the strands separate and are used as templates for the formation of complementary strands. Thus, the nucleotide sequence of F determines the sequence of a new F' strand, and F' indicates the composition of a new F strand.

<h3>DNA replication process</h3>

In the video of the amoebas sisters it is briefly explained that..

  1. DNA replication occurs in the 5' → 3' direction and the strands are separated by the action of enzymes, which break the bonds between the nitrogenous bases and unwind the strands, opening the double helix.
  2. As DNA uncoiling takes place, other enzymes act to catalyze the synthesis of two new sequences using the parent strands as a template. Each strand created joins an original strand of DNA. Therefore, the process is classified as semi-conservative.
  3. DNA is a double helix molecule and for its duplication to occur, the first step is to unpack this structure by the action of the DNA helicase enzyme. The helicase recognizes the origin of replication and works by breaking the hydrogen bonds in the nitrogenous bases A-T and C-G. This process occurs at several points and forms "replication bubbles".
  4. As the bonds unravel, it's like a zipper opening, so this step gives rise to a Y-shaped structure called the replication fork, the starting point of duplication.
  5. The primase enzyme is responsible for synthesizing a portion of RNA, called a primer. In this step, several primers are generated and are joined to the chain to start DNA synthesis.
  6. The DNA polymerase enzyme is the replication enzyme responsible for extending the new strand by adding the bases (A, C, G and T). This step is directed from the 5' end, with a phosphate group, to the 3' end, with a hydroxyl group. This phase is called continuous replication.
  7. Among the primers attached to the original strand, several pieces of DNA are attached and are called Okazaki fragments. As the sections will need to be joined later, this phase is called delayed.
  8. The exonuclease enzyme is responsible for removing the primers from the original strands after the formation of continuous and discontinuous strands. To avoid sequencing errors, a review and, if necessary, a correction is performed by another exonuclease.
  9. The enzyme DNA ligase causes the DNA fragments to be joined and the DNA sequenced into two continuous strands.

thus, in a simple way, how DNA replication occurs in the video of the amoebas sisters.

learn more about DNA in brainly.com/question/264225?referrer=searchResults

5 0
2 years ago
A woman who is a carrier for hemophilia marries a hemophiliac man. What will be their children’s possible phenotypes?
Morgarella [4.7K]

Answer:

Hemophilia is a sex-linked recessive disorder in which a person's blood do not clots and he can bleed to death even after minor injuries because blood will keep running due to a small cut.

It is a recessive trait which means that even if one normal gene is present along with Hemophiliac gene, the person will not have the disease and he will be the carrier.

Question: What will be their children’s possible phenotypes?

If a woman who is a carrier for hemophilia marries a hemophiliac man, their genotypes can be denotes as :

Here H, indicate normal gene and small h indicate defected (hemophilia) gene.

Parents:                      XHXh                   X           XhY

Offspring:                   XHXh : XHY:  XhXh:  XhY

Phenotype of offspring:

XHXh:  The child will be daughter and normal (25 % chances)

XHY:     The child will be son and normal (25 % chances)

XhXh:   The child will be girl and Hemophiliac (25 % chances)

XhY:      The child will be son and Hemophiliac (25 % chances)

Hope it helps!

5 0
2 years ago
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