Answer:
Through cultural innovation and changes in habitat and ecology, there have been a number of major dietary shifts in human evolution, including meat eating, cooking, and those associated with plant and animal domestication.
Explanation:
Dietary preferences have shifted in many ways, including:
Increased consumption of processed foods, sugar, industrial seed oils, and poultry
Decreased consumption of butter, lard
, shortening
, dairy, fresh fruits, fresh vegetables, and red meat
Increased consumption of chicken and cheese
Decreased consumption of milk and ice cream
Increased consumption of corn-derived sweeteners
Increased consumption of foods high in energy, fats, free sugars, and salt/sodium
Decreased consumption of fruit, vegetables, and other dietary fiber such as whole grains
The frequency of two alleles in a gene pool is 0.1 (A) and .9 (a). The percentage in the population of heterozygous in individuals is 18%, and the percentage of homozygous recessives is 81%.
The frequency of two alleles in a gene pool is 0.1 (A) and .9 (a). Hence,
p = 0.1 and q = 0.9
The equation for the Hardy-Weinberg principle is:
p² + 2pq + q² = 1
p² + 2pq represents the frequency of heterozygous individuals and q² represents the frequency of homozygous recessives
Substituting the values:
p² + 2pq + q² = 11 × 0.01 + 2 × 0.1 × 0.9 + 0.81 = 1 = 0.01 + 0.18 + 0.81= 1
Therefore, the percentage of heterozygous in individuals is:
p² + 2pq = 0.18 × 100% = 18%
And the percentage of homozygous recessives is:
q² = 0.81 × 100% = 81%
Thus, the percentage in the population of heterozygous individuals is 18%, and the percentage of homozygous recessives is 81%.
Learn more about Hardy-Weinberg principle here:
#SPJ2
B) It is the second-largest source of energy on Earth.
C) It is the type of energy most often used by humans.
D) It is the easiest type of energy to harvest for use.
B) sequence.
C) map.
D) contig.
Acontiguous stretch of DNA formed from overlapping DNA fragments is known as a contig. Contigs are a crucial component in DNA sequencing and genome assembly.
A set of overlapping DNA fragments that form a contiguous stretch of DNA is referred to as a contig. In molecular biology and genetics, contigs are used in the process of DNA sequencing to assemble larger sequences of DNA from smaller sequences or fragments. Creating a contig is a crucial step in genome assembly, and it is typically accomplished using computer algorithms that match overlapping ends of different DNA fragments.
#SPJ11
b. light.
c. matter.
d. heavy.
O proteins
O amino acids
O lipids
O steroid hormones