Answer:
In metaphase 1, chromosomes from the mother and father line up randomly along the middle of the cell.
Explanation:
In diploid (2n) organisms, the homologous chromosomes are the two copies of each chromosome, where one of these homologs is the chromosome from the mother, while the second one is from the father. During metaphase I, the homologous pairs of chromosomes pair together at the middle of the cell. The law of independent assortment, also known as or Mendel's Second Law, states that homologous chromosomes line up in random orientations at the metaphase plate during this period (metaphase I).
<h2><em>Why is it sometimes hard to establish an MPA?</em></h2>
- <em>Arguably, it is difficult to declare such an MPA successful, when <u>the human populations responsible for degradation have been removed</u>, and its mere establishment is rife with such political contention. Issues also arise when considering the resources needed to support a large-scale MPA.</em>
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Increases because there's more food for the carnivores, as a result, the gradually the herbivores will decrease as the reach to a point they are no longer able to feed all the predators
This process is a technique of osmosis. Osmosis is the movement of solvent particles. For example, water along its concentration gradient, from high to low concentration, via a semi-permeable membrane is changing the structure of the molecules in the potato strips.
Since the environment of the potato strips are in a sugar concentrate, the potato will lose its water content and so loses weight and the strips will be thinner and dryer.
Answer:
Inbreeding and greater chance of passing deletereous mutations through generations
Explanation:
There are several reasons why small populations are more prone to genetic diseases. One of them is that in small populations there tends to be more inbreeding
, that is breeding between individuals are closely related. Inbreeding increase the chances of offspring being affected by deletereus homozygous genotypes.
On the other hand, the acquisition of a deleterious mutation in a small population is more likely to be spread in that small population than in a large population.
