Answer:
False
Explanation:
Phylogenetic analysis is a means of establishing evolutionary relationships.
Synapomorphy is a shared ("syn") character that is different from the form found in an ancestor that distinguishes a clade (monophyletic group)from other organisms
The absence of a trait can be used as a synapomorphy in phylogenetic analysis. For example, the loss of a trait, such as the loss of legs in snakes, can be a valuable synapomorphy for a clade.
Answer;
Complementary base pairs;
- Adenine-Thyamine and Guanine-Cytosine (A-T and G-C)
Explanation;
-According to Chargaf's rule, the secondary structure of the DNA requires that every guanine pairs with a cytosine and every thymine pairs with an adenine, resulting in consistent ratios between the nucleotides.
-In double-stranded DNA, two long molecules twist around one another in a double helix. Pairs of nitrogenous bases are set in the same plane, and interact with each other via hydrogen bonding. These pairs are often referred to as base pairs
Literally all I have is humor
<span>The Cerebrum: The cerebrum or cortex is the largest part of the human brain, associated with higher brain function such as thought and action. The cerebral cortex is divided into four sections, called "lobes": the frontal lobe, parietal lobe, occipital lobe, and temporal lobe.</span>
<span>Point mutations are of two types: Substitutions of bases that are the change of one base of DNA by another. And Transitions that are replaced on a pyrrhic basis by another pyrrhic or a pyrimidine by another pyrimidine. Transversions: substitution of a pyrrhic base by another pyrimidine or vice versa. These mutations are negative because they affect only one of the nucleotides, and therefore, only one triplet of bases are affected. When the mutation does not affect the individual it is a silent mutation. Chromosomal mutations Changes in the structure of the diploid chromosomes, where one of the chromosomes has a mutation, will have another normal. They can hinder the process of meiosis in the carrier since it hinders the correct pairing of the homologous chromosomes. It would produce an unfeasible offspring or with mutations.</span>