The answer is C, because if something contagious we’re to threaten the population of the species then not having any variant means they’re all the same and it would kill them all and cause them to go extinct
Answer:
A
Explanation:
when light is limited photosynthesis will be slowed so the euglena will prefer to ingest food...light is needed for photosynthesis
Answer:
The term autotrophs refer to all plants because of their ability to undergo photosynthesis (the process of food preparation using light as a source)
Answer:
The correct answer would be 2 in 4.
According to the question Xo and XO show codominance and express themselves completely when present in heterozygous condition. Cats bearing XoXO show patchwork of black and orange fur and are called tortoiseshell cats.
Xo codes for orange color fur and XO codes for black color fur. In addition, Y chromosome does not contain any gene associated with fur color.
Now, genotype of mother cat is XOXO (orange fur). So, the gametes formed would be XO only.
The genotype of father cat is XoY(black fur). So, the gametes would be Xo and Y.
The cross would lead to the formation of two male cats each having XOY as their genotype and two female cats each with XOXo as their genotype.
Hence, both the male cats would show orange fur and both the female cats would show patchwork of orange and black fur.
Therefore, we can conclude that 2 out of 4 would exhibit tortoiseshell coloring.
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.