Answer:
The two main reasons are nonpolar core of the bilayer and the active transport.
Explanation:
The membrane is structured to have two outer layers that are polar and an inner layer that is nonpolar.
If a membrane protein is exposed to the solvent, i<em>t will also have a polar side. It would be very difficult for the polar face of the membrane to move through the nonpolar core of the bilayer.</em> Therefore, this model is not feasible.
One major form of transport, active transport, moves solutes up the concentration gradient. <em>The binding of a solute and then release on another side of the membrane would only work for facilitated diffusion because it would cause a net movement of solutes down the concentration gradient.</em> It is unclear how energy could be expended to drive this process in the transverse carrier model.<em> Therefore, the transverse carrier model does not explain active transport.</em>
Some mutations have a positive effect on the organism in which they occur. They are called beneficial mutations. ... They increase an organism's changes of surviving or reproducing, so they are likely to become more common over time. There are several well-known examples of beneficial mutations.
Answer: Stratigraphy and Biostratigraphy
Relative dating is a method of determination of age, in which one object or organism is compared with the other object or organism found in the heap of strata. It is a method for determining the relative order of the past events, without stating the absolute age.
Stratigraphy is a branch of geology that studies the relative position of the sediments and rocks in the strata with respect to the geological timescale. Biostratigraphy is the branch of stratigraphy which deals with the relative aging of fossils with respect to the strata in which these are found defining a particular period of geological time scale.
Answer:
What?
Explanation:
I don't understand the question.
Which structure are you talking about??
D. 9PM is what i would think it to be
