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solmaris [256]
2 years ago
8

Four laws or principles are involved with the study of stratigraphy. They are _____.

Biology
2 answers:
dalvyx [7]2 years ago
8 0

Answer:

law of original horizontality, law of superposition, law of original lateral continuity and law of cross-cutting relationships.

Explanation:

Before we know the principles of Stratigraphy, we need to understand what it is. To do this, let's first look at the origin of the word statigraphy: from Latin stratum means layer and from Greek graphia means field of study. From this we can understand that stratigraphy is the study of layers. Therefore, we define stratigraphy as the study of the sedimentary rock layers and it seeks to determine the processes and events that formed them.

Now that we know what Stratigraphy is, let's know its principles:

  • Law of superposition: In any succession of strata of rock (which has not been deformed), the oldest stratum is positioned lower, with the successively younger strata being positioned higher. This principle allows us to identify the order of formation of the strata, which is the basis of all historical interpretation of stratigraphic rocks.
  • law of original horizontality: Sedimentary deposits usually accumulate in horizontal layers under the influence of gravity.
  • law of original lateral continuity: Sedimentary layers are continuous, extending to the margins of the deposition basin, or tapering laterally
  • law of cross-cutting relationships: states that an intrusive or faulty rock that cuts a sequence of rocks is younger than the rocks it cuts.

soldi70 [24.7K]2 years ago
6 0

Four laws or principles are involved in the study of stratigraphy are:

1. Principle of original horizontality
2. Law of superposition
3. Law of crosscutting relationships
4. Principle of Lateral Continuity

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Gene A has two alleles (A1 and A2). A1A1 homozygotes are twice as likely to survive from birth to reproductive age as heterozygo
Usimov [2.4K]

Answer:

The correct answer is C: <em>0.60 </em><em>A1</em> and <em>0.40 A2</em> will be the allele frequencies in those progeny when they reach reproductive age

Explanation:

<em>Genotype</em>                                <u><em>A1A1 </em></u><em>  </em><u><em>A1A2</em></u><em> </em><u><em>A2A2 </em></u>

<em>Relative aptitude, w</em>                  1           0.5    0.5

<em>Number of individuals</em>                 40            40     40

<em>Initial allelic frequency</em>      p0= (40+20)/120=0.5    q0= (40+20)/120=0.5

<em>Zygote frequency</em>                  p2= 0.25 2pq=0.25 q2=0.625

<em>Relative contribution</em>         0.25x1=0.25     0.5x0.5=0.25 0.25x0.5=0.125

<em>of each genotype</em>              

<em>Average aptitude W</em>              W= 0.025 + 0.25 + 0.125 = 0.625

<em>Population</em>                    AA= 0.25/0.625    AB=0.25/0.625  BB=0.125/0.625

<em>Genotype frequency</em>             AA= 0.4             AB=0.4          BB=0.2  

<em>New Allelic frequency</em>       p1=0.4+(0.4/2)=0.6   q1=0.2+(0.4/2)=0.4

  • <em>Total number of individuals</em>: 120
  • <em>Initial allelic frequency</em>:

                  (number of homozygote individuals + half number of  

                   heterozygote individuals) / Total number of individuals

  • <em>Relative contribution of each genotype</em>:

                           Zygote frequency x Relative aptitude

  • <em>Average aptitude W</em>: It is the sum of relative contribution of each genotype to the next generation.  

                    wA1A1 x p2 + WA1A2 x 2 x p x q + WA2A2 x q2

  • <em>Population Genotype frequency</em>:

                Relative contribution of each genotype / Average aptitude

  • <em>Allelic frequency</em>:

                      Homozygote population genotype frequency +  half  

                           heterozygote population genotype frequency

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PCR refers to the polymerase chain reaction that amplifies the small sample of DNA into multiple copies in three steps. These steps are denaturation of sample DNA to produce single-stranded template strand, binding of primer to the template and elongation. The multiple copies of the sample DNA are then used to decipher its sequence using various sequencing methods.

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