The conversation between madame valmonde and desiree gives an example of Foreshadowing; situational irony;
Considering this Quote;
Madame Valmonde "shuddered at the first sight of it.....It was a sad lokking place.......The roof came down steep and black like a cowl, reaching out beyond the wide galleries that encircled the yellow stuccoed house. Big, solemn oaks grew close to it, and their thick-leaved, far-reaching branches shadowed it like a pall."
The imagery in this quote reveals the darkness of a place that is ironically called a shelter, and Madame Valmonde mentions the "pall" that is cast over the house , that being a term related to death.
The bony labyrinth is a region of dense bone that surrounds and protects the membranous labyrinth.
Labyrinth is the name given to the inner ear. It is made up of a network of interconnecting sacs and canals. The inner ear is composed of two parts: bony labyrinth and membranous labyrinth. A vestibule, three semicircular canals, and a spirally wound cochlea make up the bony labyrinth. It is perilymph-filled.
The membranous labyrinth is encircled by the bony labyrinth. It includes the hearing and balance sensory receptors. The cochlear duct, saccule, and utricle and three semicircular ducts that make up the endolymph-filled membranous labyrinth. The cristae, an organ of corti, and the ampullaris maculae are examples of sensory receptors.
To learn more about inner ear, membranous labyrinth and bony labyrinth here,
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Answer:
The correct answer is- 4:0
Explanation:
Marfan syndrome is a genetic problem which affects the connective tissue in the body. The trait for this disease is autosomal dominant which means even one abnormal copy of this gene in the offspring or individual is sufficient to cause this syndrome.
Let S is the allele that is dominant for this syndrome and s is recessive. So if a cross between homozygous dominant(SS) and heterozygous individual (Ss) occurs than all the offspring would have this syndrome.
S s
S SS Ss
S SS Ss
Therefore all 4 offspring would have at least one dominant allele which is sufficient to cause this syndrome. So the phenotype ratio would be 4:0.
