Answer:
this should help you figure this out!
Explanation:
a somewhat regular progression of species replacement is called succession consists of a community and all the physical aspects of its habitat such as the soil water and weather. Ecosystem.
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.
Protects the plant from losing water. The sharp needles of the tree mean that is has less surface area for the sun to make contact. They may also have differently shaped stomata, in order to prevent water loss
Answer:
Animal and plant respiration place carbon into the atmosphere. When you exhale, you are placing carbon dioxide into the atmosphere. Plants use carbon dioxide from the atmosphere to make the building blocks of food during photosynthesis. Carbon is found in the hydrosphere dissolved in ocean water and lakes.
Explanation:
Hope this helps.
Answer:
1. Chromatin condense into chromosomes.
4. Homologous chromosomes pair up (formation of tetrads).
5. Homologous chromosomes separate and move to poles.
2. Sister chromatids separate.
3. Chromosomes unravel in to chromatin.
Explanation:
This question portrays the process of meiosis in a cell. The ordered sequence of events in the options are:
1. Chromatin condense into chromosomes - This process occurs in the Prophase stage. Prior to the cell division, the nuclear material is found as Chromatin material. This Chromatin material then undergoes condensation to form visible chromosomes.
4. Homologous chromosomes pair up (formation of tetrads) - This process also occurs during the Prophase stage of meiosis I. In this stage, homologous chromosomes (similar but non-identical chromosomes received from each parent) are paired up side by side to form a structure known as TETRAD or BIVALENT.
5. Homologous chromosomes separate and move to poles - This process characterizes the Anaphase stage of meiosis I. Homologous chromosomes are pulled apart to opposite poles of the cell by spindle microtubules.
2. Sister chromatids separate - After meiosis I, meiosis II involving sister chromatids instead of homologous chromosomes follows. In the Anaphase stage of meiosis II specifically, sister chromatids are pulled apart towards opposite poles of the cell.
3. Chromosomes unravel in to chromatin - After the whole division process i.e. karyokinesis (division of the nuclear material), the chromosomes begin to unravel to form the CHROMATIN threads once again. This process occurs in the Telophase stage of meiosis.
