Answer:
By eating things with protein in it. Sorry if this sounds too simple, but that's all it is.
Answer:
i think its D
Explanation:
if thats wrong then im sorry lol
<span>1. Hind limes tend to be sturdier, stronger and longer. </span>
<span>2. The hind limbs are more firmly attached to the spine.</span>
Answer:
1) CO₂
2) 0.2551 g
Explanation:
The balanced reactions are:
CaCO₃ + 2HCl → CaCl₂ + H₂O + CO₂
MgCO₃ + 2HCl → MgCl₂ + H₂O + CO₂
1) The gas produced is CO₂.
2) Calculate mass of CaCO₃:
(0.5236 g) (0.4230) = 0.2215 g CaCO₃
Convert to moles:
(0.2215 g CaCO₃) (1 mol / 100.1 g) = 0.002213 mol CaCO₃
Find moles of CaCO₃:
(0.002213 mol CaCO₃) (1 mol CO₂ / mol CaCO₃) = 0.002213 mol CO₂
Convert to mass:
(0.002213 mol CO₂) (44.01 g / mol) = 0.09738 g CO₂
Calculate mass of MgCO₃:
(0.5236 g) (0.5770) = 0.3021 g MgCO₃
Convert to moles:
(0.3021 g MgCO₃) (1 mol / 84.31 g) = 0.003583 mol MgCO₃
Find moles of MgCO₃:
(0.003583 mol MgCO₃) (1 mol CO₂ / mol MgCO₃) = 0.003583 mol CO₂
Convert to mass:
(0.003583 mol CO₂) (44.01 g / mol) = 0.1577 g CO₂
Total mass of CO₂:
0.09738 g CO₂ + 0.1577 g CO₂ = 0.2551 g CO₂
Answer:
SNPs have shown that only 0.1 % of DNA sequences are different in the human genome between different individuals, thereby all the inherited phenotypic variation observed in our species is associated with only 0.1 % of differences at the genome level
Explanation:
Haplotypes are block-like sequences of DNA that are inherited together due to low recombination rates. Moreover, single-nucleotide polymorphism (SNP) mapping is a very useful methodology used to map the site of SNP mutations (i.e., SNP variants). In this regard, it has been observed that there are approximately 10 million common SNPs in the human genome. These SNPs contribute to the wide range of phenotypic variation observed in human populations for different traits (e.g., eye color, hair, weight, height, etc). Moreover, researchers have determined that SNPs can be clustered into haplotypes, thereby haplotypes can be accurately sampled by as few as approx. 300,000 selected SNPs, which are sufficient to represent all of the genetic variation across different human genomes.
