Answer: Research with embryonic stem cells may lead to new, more effective treatments for serious human ailments and alleviate the suffering of thousands of people.
Explanation:
Species with more likely homologous structures share a common ancestor.
- D. share a common ancestor.
<h3>What are example homologous structures?</h3>
The most correct definition for homology would be: They are structures of individuals, of different species or not, that were inherited from a common ancestor. The human arm is homologous to the horse's front leg. The bat's wing is homologous to the whale fin.
With this information, we can conclude that homologous have same embryological origin of structures from different organisms, and these structures may or may not have the same function
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Increasing the number of stomata per unit surface area of a leaf when atmospheric carbon dioxide levels decline is most analogous to a human
B. putting more red blood cells into circulation when atmospheric oxygen levels decline.
<h3>What are stomata?</h3>
The stomata are apertures in the epidermis, each bounded by two guard cells. There are small openings on the lower surface of the leaves. These pores are called stomata. Loss of water from the stomata creates an upward pull, that is suction pull, which helps in the absorption of water from the roots. That is helpful for the transpiration process. They help in exchange for gases. Any of the tiny pores or openings in the epidermis of leaves and young stems are referred to as a stomate, sometimes known as a stoma, the plural of which is stoma or stomas. On the underside of the leaves, stomata tend to be more numerous. They enable the exchange of gases between the atmosphere outside and the leaf's branching network of interconnected air canals.
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Part A: B
Part B: C
Hope this helps!
The independent assortment of genes is a principle of Mendel and of genetics. Since humans are diploid organisms (they have 2 copies of their genetic information), we have that each gamete carries one of the two available alleles for each feature. These gametes are created in equal proportions.
We have that both parents are heterozygous for a feature, lets say H. Thus, their genotype is Hh. Hence, the child will get with probability 50%=1/2 H from the father and 50%=1/2 h from the father; same from the mother. By doing a Punnett square, we get that there is 1/4 chance that the child is HH, 1/2 chance that it is Hh and 1/4 that is hh. Since the disease is recessive (so both alleles are needed), we have that the chance that the kid has the disease is 1/4.
