<u>Question</u>:
Which value is being measured in the columns labeled "Fraction remaining” and "Percentage remaining”?
-
years of decay
- quantity of energy
- number of stable atoms
- amount of material that has not decayed
<u>Answer</u>:
"Amount of material that has not decayed" being measured in the columns labelled "Fraction remaining” and "Percentage remaining”
<u>Explanation</u>:
The table shown below having explains about the half life , the amount of sample in both fraction and percentage. The first column named half life elapsed tells us the the number of half life that that is completed. Half life is the time taken for an element to reduce or decay into half of its initial amount.
The fraction remaining column gives the amount of sample that is left behind after the half life particular number of half life has completed. similarly the percentage remaining column gives the amount of sample in percentage. For example, the 5th row tells us that after 4 half life is over
of the sample remained. In percentage it is 6.25%
Answer:
C. Co-evolution
Explanation:
In biology, coevolution occurs when two or more species reciprocally affect each other's evolution through the process of natural selection. The term sometimes is used for two traits in the same species affecting each other's evolution, as well as gene-culture coevolution
It produces a high volume of protein as enzymes
Genetic fingerprinting – the analysis of DNA in order to identify the individual from which the DNA was taken to establish the genetic relatedness of individuals. It is now commonly used in forensic science (for example to identify someone from a blood sample) and to determine whether individuals of endangered species in captivity have been bred or captured from the wild.
<span>•DNA sequencing – the determination of the precise sequence of nucleotides in a sample of DNA or even a whole genome e.g. the Human Genome Project. </span>
<span>The process of electrophoresis: </span>
<span>DNA is chopped, close to the VNTR regions, into fragments using restriction enzymes. The DNA fragments are placed on the agarose gel and a direct current is applied continuously to the gel. The DNA fragments are attracted to the anode. The shorter the fragment, the faster it moves. </span>
<span>The fragments are transferred onto an absorbent paper placed on top of the gel. The paper is heated to separate the 2 strands in each DNA molecule. Complementary probes which have a radioactive phosphorus isotope are and this pair up with the DNA strands. The paper is placed on an X-ray film and the film goes dark due to radiation emitted by the probes. Now we end up with a pattern of dark stripes on the film matching the positions reached by the fragments in the agarose gel.</span>