<h3><u>Answer;</u></h3>
A. counterclockwise toward the center
<h3><u>Explanation;</u></h3>
- <em><u>In the Northern Hemisphere, winds associated with a low-pressure system blow in a counterclockwise direction towards the center, while those that are associated with a high-pressure system blow in clockwise direction outwards from the center.</u></em>
- In the Southern Hemisphere on the other hand, winds that are associated with a low-pressure system blow clockwise towards the center.
- <em><u>The rotation of the earth creates a force called the Coriolis force, which gives the wind that is within high pressure systems a clockwise circulation in the northern hemispheres and a counterclockwise circulation in the southern hemisphere.</u></em>
I think maybe the nephrons ...but not sure...
Independent grouping of qualities happens amid meiosis in eukaryotes. Meiosis could be a sort of cell division that diminishes the number of chromosomes in a parent cell by half to deliver four regenerative cells called gametes. In people, diploid cells contain 46 chromosomes, with 23 chromosomes acquired from the mother and a moment comparative set of 23 chromosomes acquired from the father. Sets of comparable chromosomes are called homologous chromosomes. Amid meiosis, the sets of homologous chromosome are separated in half to make haploid cells, and this partition, or grouping, of homologous chromosomes is arbitrary. This implies that all of the maternal chromosomes will not be isolated into one cell, whereas the all fatherly chromosomes are isolated into another. Instep, after meiosis happens, each haploid cell contains a blend of qualities from the organism's mother and father.
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.
