What are you asking I would love to help
Answer: False
Explanation: You're supposed to have numerically more smaller units than bigger units, since a lot of these smaller units are combined to create a single larger unit.
Answer:
- Interruption in the genetic flow between separated groups
- The emergence of new mutations in each of the groups, and their accumulation in time. Slow and gradual differentiation between populations.
- Genetic divergence by natural selection and reproductive isolation
- Prezigotic isolation mechanisms
Explanation:
Allopatric speciation consists of the geographic separation of a continuous genetic background that can give place to two or more new geographically isolated populations. These separations might be due to migration, extinction of geographically intermediate populations, or geological events. In this speciation, some barriers impede genetic interchange, or genetic flux, as the two new groups that are separated can not get together and mate anymore. These barriers might be geographical or ecological.
The process of allopatric speciation involves different steps that affect organisms:
- The emergence of the barrier.
- Interruption in the genetic interchange
- The occurrence of new mutations and their accumulation in time in each population. Slow and gradual differentiation.
- Genetic divergence by natural selection and reproductive isolation makes it impossible for the two groups to mate even if the barrier disappears.
- Prezigotic isolation mechanisms will be favored by selection if occurs a secondary contact between the new species in formation.
Answer:
carbohydrates- store energy and provide support and help in mating the energy sorted in the body
lipids- surround and protect cells, regulate cell fucntions and the body and the organism.
Simple version:
First, the section with the desirable gene must be identified. Assuming that has already happened, the section of DNA must be excised from the original genome using restriction enzymes, which recognize certain DNA sequences and snip DNA at those sites. DNA ligase is used to "glue" these ends back together. The DNA is inserted into a plasmid (also with restriction enzymes), which would usually contain antibiotic-resistance genes (so they survive in an environment containing the antibiotic, which would also help show if the bacteria have been successfully transformed).
Then comes the actual transformation process. The bacteria to be transformed are mixed with calcium chloride (which causes the bacteria to be more receptive to the plasmids) and then mixed with the plasmids. The bacterial cells are subjected to a heat shock (the solution is heated and rapidly cooled, e.g. by placing the mixture in a hot water bath and quickly transferred to ice) so they will take up the plasmid (since the temperature change makes the membrane more permeable). The bacteria are placed on a growth medium containing the antibiotic they're resistant to. Only those successfully transformed would survive.
