Answer:
The genotypic frequency = 1:1
The phenotypic frequency = 1:1
Explanation:
Given that:
The allele → R = Red beetles
The allele → B = Blue beetles
Since the gene color shows a codominant allele
The Red Beetle = RR
The blue beetles will be = BB
The heterozygous beetle will be = RB
∴
The punnet square showing the crossing of RB × RR is:
R B
R RR RB
R RR RB
The result shows that we have two red beetles and two heterozygous beetles.
Hence;
The genotypic frequency = 1:1
The phenotypic frequency = 1:1
Answer:
<em>Volume</em><em>(</em><em>v</em><em>)</em><em>=</em><em> </em><em>l</em><em>×</em><em>w</em><em>×</em><em>h</em>
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<em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em>=</em><em> </em><em>1</em><em>2</em><em>0</em><em>0</em><em>0</em><em>cm</em><em>^</em><em>3</em><em> </em>
<em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em> </em><em>ans</em><em>.</em>
Photosynthesis makes the glucose that is used in cellular respiration to make ATP. The glucose is then turned back into carbon dioxide, which is used in photosynthesis. While water is broken down to form oxygen during photosynthesis, in cellular respiration oxygen is combined with hydrogen to form water.
Answer:
Autosomal dominant inheritance: A person affected by an autosomal dominant disorder has a 50 percent chance of passing the mutated gene to each child. The chance that a child will not inherit the mutated gene is also 50 percent. However, in some cases an autosomal dominant disorder results from a new mutation that occurs during the formation of egg or sperm cells or early in embryonic development. In these cases, the child's parents are unaffected, but the child may pass on the condition to his or her own children.