The
statement that best supports that belief is “both have cell wall made
of cellulose, store food material as starch, and have chlorophyll a and chlorophyll
b”.
The green algae are a
large, informal grouping of algae consisting of the Chlorophyte and Charophyte
algae, which are now placed in separate Divisions. The land plants or
Embryophytes are thought to have emerged from the Charophytes.
The correct answer between all
the choices given is the first choice or letter A. I am hoping that this answer
has satisfied your query and it will be able to help you in your endeavor, and
if you would like, feel free to ask another question.
Cyanobacteria were very simple organisms and performed were an role in changing Earth's early atmosphere. They carried out photosynthesis to produce the materials they needed to grow. In this process, they release Oxygen which is needed to sustain life on Earth for Humans and other organisms.
The correct answer is Karl will get sick and Jose will not this time, but neither will get this influenza again since they both will have acquired active immunity to it.
In the case of Jose artificially active immunity has been induced due to vaccination. A vaccine instigates a primary response against the antigen without resulting in any signs of the disease. On the other hand, Karl will acquire active immunity naturally in future, as when an individual get exposed to a live pathogen, he or she develops the disease, and turns immune as an outcome of the primary immune response.
Answer: DF508 mutation. A Genetic, Hereditary, Autosomal and Recessive Mutation.
Explanation:
Cystic fibrosis (CF) is a recessive autosomal lethal disease, it is most common on Caucasoid populations. Its diagnosis is suggested by the clinical features of chronic obstructive pulmonary disease, persistent pulmonary colonization (particularly with mucoid Pseudomonas strains), meconium ileus, pancreatic insufficiency with or familiarity history of the disease. The FC gene is large, with about 250 Kb of genomic DNA, 27 exons representing about 5% of genomic DNA; encodes a 6.5 kb transcribed mRNA. This mRNA is transcribed into a protein of 1480 amino acid called CFTR (Regulator Transmembrane Conductance Cystic Fibrosis). When a three-base pair deletion, adenosine-thymine-thymine (ATT) identified in the CFTR gene, exon 10, it results in the loss of a single amino acid phenylalanine at position 508 of the protein. This mutation is called DF508; “D” stands for deletion and “F” for phenylalanine amino acid.
