Answer:
The lion population would decrese
Explanation: The more hyenas would mean more competion for food which would lead to lions dieing off due them not being able to get food hope this helps god bless
D hurricanes makes the most sense because lightning isn't and blizzards have nothing to do with ocean waters and tornadoes only occur inland.
1. Enzyme is the molecule that serves to make reactions work. Enzymes are biochemical catalysts that catalyses chemical reactions in a cell by acting on substrates and convert them to products. Their rate of action increases with increase in substrate concentration, reaching optimum when all active sites of the enzyme are engaged.
2. Plastid are the tiny sacs in the cell that may contain starch. Plastid are major cell organelles found in the cells of plants and algae. Plastids are site for the manufacture and storage of important chemical compounds used by the cell. They often contain pigments used in photosynthesis, and the types of pigments present can change or determine cells color.
3. Lysosome are packets within the cell that contain digestive enzymes. Lysosomes are one of many organelles found in animal cells. they are tiny like sacs filled with enzymes that enables the cell to process nutrients. They contain digestive enzymes which helps in the digestion of worn out organelles, food particles and engulfed viruses or bacteria.
4. Mitochondrion is a structure within a cell that is responsible for production of energy. Energy in a cell is produced through a process of cellular respiration which involves use of nutrients with oxygen gas to yield energy inform of ATP, water and carbon dioxide. The process takes place in the mitochondrion where oxygen acts as proton acceptor in the electron transport chain coupled by production of energy.
5. An Organelle is a small structure that serves specialized functions. A cell is made up of various organelles that help it perform its functions. Each organelle is specialized to perform as specific function different from other organelles, for example ribosomes is an organelle involved in the manufacture of proteins.
6. Golgi apparatus are group of flattened sacs that package and export materials out of the cell. Golgi apparatus also called golgi complex or golgi body, is a membrane bound organelle in eukaryotic cells that is made up by a series of flattened, stacked pouches called cisternae. They are responsible for transporting, modifying, and packaging proteins and lipids into vesicles.
7. Vesicles are tiny sacs connected to the Endoplasmic reticulum and Golgi apparatus. Vesicles are small structures within a cell, or extracellular, consisting of fluid enclosed by a lipid bi-layer. they form naturally during the process of secretion (exocytosis), uptake (endocytosis) and transport of materials within the cytoplasm.
Answer:
The female will not inherit a sex linked disorder if her father suffers rather "have chances or the disorder if the mother is the carrier" for the disorder.
Explanation:
A female has 2 X chromosome, which she got from her parents each. The females will get the disorder or the defective gene if the mother has defective X chromosome or if the father is carrying the same disorder from his father(grandfather). In both the cases the female will be the carrier and have chances to inherit the defect to the offspring. But the female will not affect as the male will. As the female has 2 X chromosomes, and hence the dominant X will compensate for the error in recessive X.
Addition or deletion of nucleotides in any number besides 3 results in a "frame-shift mutation."
This is because every 3 nucleotides of DNA/mRNA exons codes for a single amino acid in the synthesis of a protein. This triplet codon theory means that if 3 nucleotides are added or deleted then an amino acid will be added or lost, but subsequent codons and amino acids will still be read correctly.
However, if any number of nucleotides other than 3 are added or removed, then the codons following the mutation will be out of "sync," in terms of the reading order.
Hence it is called a frame-shift mutation because it shift the reading frame when translating nucleic acids into proteins. Frame shifts will lead to the wrong amino acids being adding in the wrong order for the rest of the code after the mutation.
