Answer:
yes
Explanation:
In the oceans on either side of the Isthmus of Panama are 30 species of snapping shrimp, 15 species on the Pacific side and 15 different species ch the Atlantic sid. See different water depths. Morphological and genetic data show that Atlantic and Pacific species that live at similar depths are sister species. Geological evidence indicates that the Isthmus of Panama started rising about 10 million years ago and the oceans were completely separated by the stimus about 3 million years ago. If the geological evidence has been misinterpreted and the isthmus had formed very rapidly in less than 1,000 years), which of the following predictions is most likely?
A. greater percentage of difference in DNA sequences between sister species that inhabit deep water than between sister species that inhabt stalow water
B. greater percentage of difference in DNA sequences between sister species that inhabit shallow water than between sister species that inhabit deep water
C. similar percentages of difference in DNA sequences between all pairs of sister species
D. greater percentage of difference in DNA sequences between Atlantic species than between Pacific species
Answer:
The answer is "Choice A".
Explanation:
The Panama isthmus is indeed a patch of land which separates its sea from its Atlantic ocean to The pacific in two halves. The Panama Isthmus allows spreading the seafood applicable state, although due to geographical barrier, the very same turtle species were isolated. Its deep squirrels of liquid are diverged quite early as being against shallow water shrimps which are characterized by the rising of the Jamaica isthmus, first off the island can be crossed until it was closed through shallow water prawns and shallow-water animals. If Panama's black sea was established less than 1000 years, it has a greater effect on deepwater shrimp and very low water lobsters. Consequently, in water depth prawns, a disparity in hereditary degree (DNA) is higher than in shallow species. The deep waters have been affected earlier so the variation in DNA sequences throughout all sister species will not be the same.
I NEED HELP ASSAP
how can you tell whether two magnets will attract eachother, repel eachother, or both
plz explain in a few sentences​
Answer:
Explanation:
there is a positive side and a negitive side to magnets two of the same side of the magnet will repel oppisites will attract
positive+positive=repel
positive+negitive=atract
Answer:
attract: when two magnets will attract, S and N will be facing each other
repel: when two magnets will repel, S and S or N and N will face each other
both: when two magnets will attract and repel, the magnets won't be placed in the same way. N will be facing the middle of both S and N or S will be facing the middle of N and S
Explanation:
this is what i learned i hope it's right if not i didn't say nothing
What is a subduction zone and a transform boundary?
a transform fault or transform boundary is a fault along a plate boundary where the motion is predominantly horizontal. it ends abruptly where it connects to another plate boundary, either another transform, a spreading ridge, or a subduction zone.
what is the speed of a car that travels 485 meters in 15 seconds
What characteristics make dna a polymer ?
Number 8. was colorblind just like his father: Where did the son at 8 get his allele for colorblindness?
Answer:
son 8 inherited it from her.
Explanation:
Given that Son 8's mother is a carrier of the blindness allele
Assuming that the father is colorblind due to a genetic mutation, there are a few possible scenarios for how the son inherited the allele for colorblindness.
What is genetic inheritance?Genetic inheritance is the study of how certain inherited traits are passed down from generation to generation.
Assuming the father is colorblind due to a genetic mutation, there are a few possibilities for how the son inherited the colorblind allele:
His father's colorblindness allele was passed down to his son. The son in this case inherited the mutation from his father.The mother carries the colorblindness allele, which she passed on to her son. In this case, the son inherited the mutation from his mother, who is not colorblind but carries the gene.The colorblindness mutation is present in both the mother and father, and the son received one copy from each parent. This is a less likely scenario, but it is possible if both parents carry the gene.Thus, in any of these scenarios, the son inherited the allele for colorblindness from one or both of his parents.
For more details regarding inheritance, visit:
https://brainly.com/question/29679846
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What are CD4 cells?
a. T-cells that have a CD4 receptor
b. B-cells that have a glycoprotein receptor
c. HIV antigens
d. red blood cells
Answer:
I'm pretty sure it is b because CD4 cells are the cells that are a glycoprotein
Explanation: