The bottleneck effect is the correct answer here. The effect is defined as a sharp reduction in a populations size due to an environmental effect. In this scenario, the asteroids were the environmental effect and it caused the Freg population to decrease significantly. Also, none of the other answers are real theories.

Genetic drift is a direct result of independent assortment. Since genes are not inherited by any organized mechanism, there are random fluctuations during which certain alleles experience an increase in frequency over others.

Genetic drift results in random changes in allele frequency; these changes are not a cause of genetic drift. In smaller populations and extreme cases, random changes can result in the loss of an allele entirely within the population. The results of genetic drift are more prominent in smaller populations due to their already reduced gene pool. Since genetic drift is random, both beneficial and harmful alleles can be promoted or eliminated.

Genetic drift cannot increase genetic diversity. The only way to increase genetic diversity is by the introduction of new traits and alleles. Genetic drift can reduce genetic diversity by eliminating alleles from a population, but is incapable of creating new traits. This can only be done through mutation.

During prophase I homologous chromosomes will line up with one another, forming tetrads. During this lining up, DNA sequences can be exchanged between the homologous chromosomes. This type of genetic recombination is called crossing over, and allows the daughter cells of meiosis to be genetically unique from one another.

Crossing over can only occur between homologous chromosomes. Cells become haploid after meiosis I, and can no longer perform crossing over.

Crossing over is a process that happens between homologous chromosomes in order to increase genetic diversity. During crossing over, part of one chromosome is exchanged with another. The result is a hybrid chromosome with a unique pattern of genetic material. Gametes gain the ability to be genetically different from their neighboring gametes after crossing over occurs. This allows for genetic diversity, which will help cells participate in survival of the fittest and evolution.

When chromatids "cross over," homologous chromosomes trade pieces of genetic material, resulting in novel combinations of alleles, though the same genes are still present. Crossing over occurs during prophase I of meiosis before tetrads are aligned along the equator in metaphase I.

By meiosis II, only sister chromatids remain and homologous chromosomes have been moved to separate cells. Recall that the point of crossing over is to increase genetic diversity. If crossing over did not occur until sometime during meiosis II, sister chromatids, which are identical, would be exchanging alleles. Since these chromatids are identical, this swap of material would not actually change the alleles of the chromatids.

During crossing over, homologous chromosomes come together in order to form a tetrad. This close contact allows the nonsister chromatids from homolgous chromosomes to attach to one another and exchange nucleotide sequences. The word "nonsister" implies that the chromatids have the same genes, but are not exact copies of one another, as they come from separate chromosomes.

The crossing over of homologous chromosomes occurs in prophase I of meiosis. Prophase I of meiosis is characterized by the lining up of homologous chromosomes close together to form a structure known as a tetrad. A tetrad is composed of four chromatids.

Anaphase I is marked by the separation of homologous chromosomes, whereas in anaphase II there is the separation of sister chromatids. In anaphase I sister chromatids are still intact and connected at the centromere. Prophase II is similar to prophase in mitosis in that there is the break down of the nuclear membrane and the formation of spindle fibers in preparation for the separation of sister chromatids.

The tetrad, which divides into non-sister chromatids, exchanges genetic information in order to make the genetic pool more variant, and result in combinations of phenotypic traits that can occur outside of linked genotypic coding.

During prophase I, homologous chromosomes pair with each other and exchange genetic material in a process called chromosomal crossover. The exchange occurs in segments over a small region of homology (similarity in sequence, ie., the same alleles). The new combinations of DNA created during crossover provide a significant source of genetic variation.  

Crossing over occurs when chromosomal homologs exchange information during metaphase of Meiosis I. During this stage, homologous chromosomes line up on the metaphase plate and exchange genetic information.