Answer:
i think its plants
Explanation:
species
phyla
genera
A genus is subdivided into smaller groups called species. Therefore, option (B) is correct.
Taxonomy is the study and practice of categorizing or classifying. A taxonomy (or taxonomical classification) is a categorization scheme, especially a hierarchical classification, that organizes things into groups or kinds.
There are seven primary taxonomic ranks: kingdom, phylum, class, order, family, genus, and species. In addition, domain, which was proposed by Carl Woese, is now commonly used as a fundamental rank, although not being listed in any of the nomenclature laws, and is synonymous with dominion.
A genus is a taxonomic rank composed of species grouped based on shared features (having similar structures or dissimilar characteristics) or evolutionary relationship. It is one of the eight major taxonomic ranks used to classify living organisms. It is subordinate to the family and superior to the species.
Learn more about taxonomical classification, here:
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Clams and squid have been evolving separately for a shorter time than clams and snails.
Clams and snails have more in common genetically than clams and squid.
Clams and snails are more similar in related structures than clams and squids.
Answer:
The correct answer is the second statement.
Explanation:
The molecular clock refers to a procedure in molecular evolution that associate the time of divergence between the two species with the number of molecular differences determined between the sequences of DNA or proteins.
The more genetically associated, the shorter will be the separation time between the two species. Due to this, as clams and squid are more closely associated it can be concluded that these species look more genetically identical, and have evolved distinctly for a brief time duration in comparison to the clams and snails.
Answer:
B. Clams and squid have been evolving separately for a shorter time than clams and snails.
Explanation:
Edge 2021
Answer:yes
Explanation:
No
Answer:
Proteins
Explanation:
Answer:
A
Explanation:
The reason the deletion of a nucleotide can be a lethal mutation is that it causes a frameshift mutation. This is due to teh fact that the codon sequence on the DNA is shifted by a single nucleotide. Therefore, the codons will read differently downstream from the place the deletion happened. The amino acids coded for by these codons will change too. The translated proteins will be defective and the organisms will be adversely affected, phenotypically.
The most dangerous mutation to a cell among the given choices would be the deletion of one nucleotide. This could result in a frameshift mutation, which can change every subsequent codon and potentially lead to a non-functional protein.
In the context of mutations and their potential harm to a cell, between the options of deletion of one nucleotide, deletion of three nucleotides, or substitution of one nucleotide for another, the most dangerous would likely be the deletion of one nucleotide.
Mutations including deletions or insertions can cause a frameshift mutation if the number of nucleotides added or deleted is not a multiple of three. For each set of three nucleotides, called a codon, corresponds to a single amino acid. A deletion of one nucleotide would shift the reading frame, potentially changing every subsequent codon and thus every subsequent amino acid in the sequence. This can result in a non-functional protein, and therefore, have significant detrimental effects on the cell.
In contrast, the deletion of three nucleotides (a complete codon), would only result in the loss of a single amino acid in the produced protein, which may or may not significantly impact the function of the protein. Similarly, while a substitution could potentially alter the amino acid specified by the affected codon, this is less deleterious than a frameshift mutation.
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