The survival of the 2 percent of the population is due to the presence of a gene obtained from other species. This gene must be responsible for developing resistance in the insects, against the insecticide that was used by the farmer. The gene got incorporated in only 2% of the insects and therefore, they survived and rest of them were susceptible to the insecticide and thus, died.
Answer:
2, 6 are the one you should select
Explanation:
The phase after ovulation (release of an egg) is called luteal phase. The stimulating follicle hormone (fsh) and luteinizing hormone (lh) are produced in the pituitary.
The FSH promotes the growth of an egg in the follicle while the LH facilitates its release from the follicle. Once the egg is released, the two hormones decrease, resulting in the rise of estrogen and progesterone.
Answer:
Option 2.
Explanation:
The fossil proof for the human-chimpanzee last common ancestor (LCA) is rare and scarce due to: These apes lived in an environment of tight or narrow range that was not preserved well in the fossil record.
Fossil monkeys and prosimians were rare in the Miocene, however, apps were normal and dominant. Option 1 is inaccurate.
The majority of the apps known from the mid-Miocene are Old World monkeys, who are from an unexpected Linnaean family in comparison to we are is an incorrect statement so it is inaccurate.
The LCA lived in the Paleocene, a time from which we have got a number of the fossil record. so Option 3 is incorrect
Thus, the correct answer is - These apes lived in an environment of tight or narrow range that was not preserved well in the fossil record.
Answer:
Its is a lysosomal storage disease!
Explanation:
<u>Hurler syndrome:-</u> is also known as mucopolysaccharidosis-I .
It Is due to the mutation on chromosome 4 .
There is a lack of of enzyme called alpha-L-iduronidase.This enzyme is present in lysosomes
It causes accumulation of mucopolysaccharides because of the absent of the enzyme in the lysosome
<u>Hunter syndrome:- </u>is also known as mucopolysaccharidosis-II
It occurs due to mutation in iduronate-2-sulfatase (IDS) gene.It is an X-linked disease
