Jun 12, 2015 · View Notes - Module 7 Lecture Quiz from MODULE 7 at University of Florida. Question1 1/1pts Ifp=.9,whatisthefrequencyoftheheterozygote? .81+(2)(.9)(.1)+(.01) .10 .81 ...
Jun 21, 2019 · 1 / 1 pts Question 11 Which of the following is NOT a reason why genetic variation matters? provides raw material for natural selection to act on if the population is faced with a …
Nov 21, 2017 · Anatomy and Physiology. Anatomy and Physiology questions and answers. 1. Which of the following is NOT a reason for genetic variation within the human population? the …
Crossing over plays a critical role in increasing the genetic variation among offspring of sexual reproduction. Crossing over is unique to meiosis. Its occurrence depends on specific events …
The transmission of traits from parents to offspring is called heredity.
Each chromosome contains one long molecule of double-stranded DNA and proteins. True
During metaphase I, there will be four pairs of chromosomes (tetrads) aligned at the metaphase plate.True
chromosome alignment in metaphase I and separation in anaphase I
Can you recognize the eight stages of meiosis based on the location and behavior of the chromosomes?
Another important aspect of meiosis and the sexual life cycle is the role these processes play in contributing to genetic variation. Although offspring often resemble their parents, they are genetically different from both of their parents and from one another. The degree of variation may be tremendous.
The parent cell that enters meiosis is diploid, whereas the four daughter cells that result are haploid.
Because lethal dominant genes are always expressed and result in the death of the embryo, fetus, or child , dominant gene disorders are NOT seen among adults.
Hereditary characteristics are transmitted to offspring by genes.
A person's genetic makeup is referred to as his or her phenotype.
Both of Jason's parents are homozygous dominant for tall. Jason has inherited the homozygous dominant trait for tallness. Jason, however, is quite short. Which of the following could explain why Jason is short?
No, because genetic diversity has nothing to do with the sex chromosomes but is due to crossing-over of chromosomes, independent assortment of chromosomes, and segregation of chromosomes. In meiosis the spermatozoa that are produced are genetically unlike each other and unlike the cell that produces them.
T or F: Horizontal gene transfer is common in both eukaryotes and prokaryotes.
T or F: DNA duplication events always lead to the evolution of genes with new functions.
Genes that are similar in their nucleotide sequence because of a common ancestry. (the key to homologous genes is not just their similarity, but that they are similar because they share a common evolutionary origin. Around half of our genes have clear homologs in flies and worms.)
C. A gene that has recently been duplicated in the genome
T or F: Homologs of many human genes are easy to detect in such organisms as worms, fruit flies, yeasts, and even bacteria.
T or F: Most genes in the genomes of vertebrates exist in multiple versions.
D. Exon shuffling requires the presence of introns.
D. Mutation is the ultimate source of novel variation.
A. Characteristics are inherited from parent to offspring.
B. Snakes on an island that are unbanded survive better than banded snakes because they avoid predation.
D. Finches with large beaks survive and reproduce more after a drought.