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sladkih [1.3K]
2 years ago
14

Which hormone is responsible for the development of the male secondary sex characteristics? estrogen progestin progesterone test

osterone.
Biology
1 answer:
netineya [11]2 years ago
6 0

Answer:

Testosterone

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ch4aika [34]

Nocardia is important in bioremediation process because they can decompose polycyclic aromatic hydrocarbons, polychlorinated biphenyls, chlorophenols, sulfonated azo dyes and alkanes.

<h3>What is bioremediation?</h3>

Bioremediation is the process of using living organisms such as microorganisms to degrade wastes in the environment in order to return it to its previous healthy state.

An example of a microorganism used in bioremediation is Nocardia spp.

Nocardia is important in bioremediation because they can decompose polycyclic aromatic hydrocarbons, polychlorinated biphenyls, chlorophenols, sulfonated azo dyes and alkanes.

Based on the complete question which is given as follows:

"Nocardia are of particular interest to scientists for the process of bioremediation because they can degrade _________. (Check all that apply) A. petroleum Hydrocarbons B. rence benzone C. pectin Keratin D. Decode Chiron", the correct options are A and B.

Learn more about bioremediation at: brainly.com/question/16922237

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2 years ago
A color-blind (X-linked recessive) human with Klinefelter syndrome has parents both of whom have normal color vision. 4a. From w
sineoko [7]

The extra X chromosome is received from mother.

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Klinefelter's syndrome is the condition of chromosomal aberration where the person has an extra X chromosome. This means the genotype of the person is 44+XXY and the total chromosome number is 47. This condition is achieved due to inappropriate meiotic division and one of the sperm or ovum has the an extra X chromosome.

Here both the parents are normal in terms of colour vision. So the father cannot have the gene of colour blindness because if it was present, then father would have been colour blind because he has only one X chromosome per cell. So its present in mother who is heterozygous in terms of colour blind gene. So the extra X chromosome also came from her which made the presence of two defective X chromosomes in the offspring and made it colour blind.

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