Deltas
erosion
sand dunes
(not sure about this one) key currents
1. The main aim of the Human Genome Project was to determine the DNA Sequence of every human gene.
2. Variation in skin colour is an example of polygenic inheritance
This Human Karyotype is unusual because it has an extra chromosome at chromosome 21.
Klinefelters syndrome is shown in the second figure
Explanation:
1. The Human Genome Project's main goal was to sequence all the 30,000 genes and 3 million base pairs in their makeup for the early detection of diseases, gene therapy and molecular level studies.
2. Human skin colour is determined by the pigment melanin. The Dominant allele is responsible for dark colours as it produces more melanin. The melanocortin 1 receptor (MC1R) gene and Tyrosinase enzyme codes for the human skin colour. Polygenic inheritance are the traits which are controlled by one or more genes.
<u>figures:</u>
<u>The extra chro</u>mosome at the 21st chromosome pairs is called trisomy 21 or Down's Syndrome. It is due to the abnormal cell division/meiosis resulting in an extra X chromosome. This leads to thechanges the in physical development of the individual.
Klinefelter's Syndrome: There are 47 chromosomes and 2 or more X chromosomes in this syndrome of males. The resulting male suffering from Klinefelter would be sterile and have poorly developed testicles.
Answer: B
Explanation:
Ammonia is so toxic that it can be transported and excreted only in large volumes of very dilute solution. As a result most terrestrial animals simply don't have access to sufficient water to routine excrete ammonia.
The main advantage of urea is its very low toxicity. Animals can transport urea in the circulatory system and store it safely in high concentrations. Also much less water is loss when a given quantity of nitrogen is excreted in a concentrated solution of urea than would be in a dilute solution of ammonia.
Minerals would be a reasonable explanation to this scenario
My opinion is on Minerals
Answer=Minerals
