It is assumed that organisms with similar anatomical characteristics have evolved relatively recently and have a common ancestor.
<h3>How does comparing the physical characteristics of different creatures help us understand evolution?</h3>
To comprehend how living things originated, scientists study the anatomy, embryos, and DNA of various species. Homological structures provide proof of evolution. These are features that were passed down from a common ancestor and are shared by related creatures. An further piece of evidence for evolution is offered by similar structures.
<h3>What role does anatomy play in the study of relationships between various types of organisms?</h3>
Comparative anatomy, which compares structural similarities, is one of the strongest types of evidence of creatures to ascertain the links between them throughout evolution. It is assumed that organisms with similar anatomical traits have evolved from ancestors who were reasonably closely connected to one another.
To know more about genomes structures visit :-
brainly.com/question/19548636
#SPJ4
Fossils can be classified by their morphology (how they look), ethologically (how they acted), and toponomically (where they are in the substrate layers) to produce phylogenetic trees. However, more recent advances in genetic technology allow us to extract DNA from more recent fossils that have not had too much breakdown of the DNA, and we can much more accurately classify species from that information, and also provide much more accurate phylogenetic analysis.
That it’s rock solid inside but outer core is liquid ?
Answer:
Explanation:
A woman who is a carrier for #1 hemophilia and a man that does not have the
condition have children. What is the probability that they will have a child
with the condition being studied? What is the gender of that child?
if the baby gets the Y chromosome from the father it will be a boy. If the boy gets his mother's X chromosome with the hemophilia gene he will have hemophilia. If he inherits his mother's other X chromosome, he will have normal blood clotting. If the baby gets the X chromosome from the father it will be a girl.
#4 A woman that is heterozygous for type A blood and a man that is heterozygous for type B blood have children. What are the possible blood types of their children?
One parent with A and another with B can produce a child with A, B, AB or O blood types.
#5 Two people are both unknowingly carriers for the cystic fibrosis gene. What is the probability that they will have children with cystic fibrosis?
If both parents are carriers there is a 1 in 4 (25 percent) chance that both will pass on the non-functioning gene, which would result in a pregnancy affected with cystic fibrosis.
#3 A woman that is heterozygous for Huntington's disease and a man that does not have the condition have children . What is the probability that their children inherit the Huntington's gene ?
Huntington's disease (HD) is what is called a dominant genetic disease. What this usually means is that a child only has a chance of getting a disease like this if a parent has it too. But parents without HD can have a child with HD. This is true of any dominant genetic disease
Answer:
# changes into water vapour
#condenses
#rain
Explanation:
As water vapor rises higher in the atmosphere, it begins to cool back down. When it is cool enough, the water vapor condenses and returns to liquid water. These water droplets eventually gather to form clouds and precipitation.
