Active transport requires energy because it moves molecules across a membrane to a region of lower to higher concentration which is often against their concentration gradient or has an obstructing factor.
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.
Answer: A. ancestral trait
Explanation:
Bipedalism can be define as a form of terrestrial locomotion, in which the organism moves with the help of two rear limbs or legs. Typical bipedal movements includes the hoping, running and walking. The evolution of the human bipedalism occurred in primates in about 4 million years ago with Sahelanthropus (oldest human ancestors or African Apes). The human ancestor Sahelanthropus led to the morphological alterations in the human skeleton including changes in the bones such as size of the bones of the foot, knee size, shape and orientation of the vertebral column, and leg length. All these changes contributed to the bipedalism.
