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Mandarinka [93]
3 years ago
11

12. The Chloroplast(Organelle) is found in the a. Autotrophs b. Heterotrophs c. Volcanoes d. Sunlight​

Biology
1 answer:
Oliga [24]3 years ago
3 0

Answer:

Chloroplasts are found in autotrophs

Explanation:

since the chloroplast contains chlorophyll which aids in photosynthesis

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PLEASE HELP ASAP (: question in photo
Misha Larkins [42]

Answer:

A) exponential growth

Explanation:

5 0
3 years ago
What is the name of the cell that activates CD4 and CD8 cells?
julsineya [31]

Hey there! Let's solve the problem:

CD4 T cells activate CD8 T cells through an underhanded cycle including an antigen presenting cell (APC), customarily a standard dendritic cell (DC). An APC presents a peptide to a true CD4 T cell through a Class II MHC molecule.

5 0
3 years ago
Describe the change in genetic variation in the population between 0 and 6 months and provide reasoning for your description bas
DochEvi [55]

Answer:

The description indicates that Genetic variation is decreasing  

The reasoning is that SEM is progressively smaller

Explanation:

Genetic variation decreases when organisms mate between relatives

4 0
3 years ago
An individual who displays the disease sickle-cell anemia must have inherited the deleterious allele from both phenotypically no
Dvinal [7]

Answer:

Homozygous recessive

Explanation:

The parents of the individual displaying the sickle cell anemia (SS) are phenotypically normal parents meaning, both parents are carriers of the (AS) gene which is a recessive trait for sickle cell anemia.

The individual took up the SS allele from both parents which makes him/her homozygous recessive. An individual is said to be homozygous recessive if that individual carries two copies of the same recessive allele.

Homozygous dominant is when an individual carries two copies of the same dominant allele (e.g AA).

5 0
3 years ago
Read 2 more answers
What must be the genotype?​
Sonbull [250]

Answer:

XnY

Explanation:

II-2 is a male so the genotype must have a Y in it. Majority of the other options do not have Y, so they are incorrect. Because the individual is male, the father has passed a Y chromosome, while the mother has passed an X chromosome. The X chromosome is Xn because the mother is hemolytic, which is a recessive trait. So both the mother's X chromosomes carry the hemophilia trait.

7 0
3 years ago
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