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Luden [163]
4 years ago
9

Why is soil important to plants? a. It provides them with nutrients. b. It provides them with water. c. It provides them with a

medium for growth. d. All of the abov
Biology
2 answers:
Butoxors [25]4 years ago
8 0

I believe the answer is A. I hope this help :)

denis23 [38]4 years ago
8 0

i think the answer is A not for sure.

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my favorite part is having fun with my friend... what you like to do? A. Party fun day B. holidays C. have a spa day D. have fun
PSYCHO15rus [73]

Answer:

A. Party fun day (relaxing)

5 0
3 years ago
In a hypothetical breed of dogs, coat color is controlled by two genes. There are six different coat colors in this breed: black
Andru [333]

The correct statements are C and F.  

There are two elementary types of pigments, which are responsible for the color of the coat, that is, phaeomelanin and eumelanin. Eumelanin is basically a black pigment and cells produced by it are responsible for a black dog coat color. However, there are genes that result in changes in eumelanin to produce brown, gray, or dusty pale brown coat color. The genes responsible for this change leads to the modifications in the creation of the eumelanin in the cells.  

Due to this reason, dusty pale brown and gray dogs are considered as dilutes. Eumelanin can also be witnessed in eyes and nose. On the basis of the genes in dogs, the nose can be brown, black, dusty pale brown, or gray. The other pigments, that is, phaeomelanin is red. Most of the dogs exhibit both phaeomelanin and eumelanin, and the manner in which these two pigments get amalgamated is controlled by agouti locus.  

The white color in dogs is not stimulated by any pigment, but by the cells that do not possess the capability to produce any kind of pigment. The entire animal can be affected in a different manner to albinos, or it can be restricted like the white coat patterns.  

The correct statements regarding the mode of inheritance of the coat color genes are:  

1) One of the genes modifies the expression of the other.  

2) One of the genes is autosomal, and the other is X-linked.  

8 0
3 years ago
Individuals with a mutation in the gene for apolipoprotein B-100 produce very low levels of this protein, which is a component o
Ksenya-84 [330]

Answer:

Fats would accumulate in the liver and the individual would show hypocholesterolemia

Explanation:

Familial hypercholesterolemia is a genetic disorder caused by a reduction and/or defect in the low-density lipoprotein (LDL) receptor. Moreover, apolipoprotein B is the unique protein component of LDL, which plays a critical role in lipid metabolism by binding the LDL receptor. Familial defective apolipoprotein B-100 refers to an inherited disorder associated with mutations of the apolipoprotein B-100 that leads to moderate or severe cases of hypercholesterolemia. Mutations in apolipoprotein B-100 are associated with a reduction in the binding capacity of LDL to the LDL receptor, thereby leading to hypercholesterolemia.

7 0
3 years ago
ok so can someone explain the Trophic Levels/Trophic Pyramid​? I would prefer it simplified for a PowerPoint but its alright lol
Georgia [21]
So the trpohic pyramid is basically the producers and secoundary abs primary consumers and all that but what comes first so the weakest animals that the animals eat above it
5 0
3 years ago
Read 2 more answers
When you eat a large meal and your body absorbs a lot of glucose and that makes its way to the interstitial fluid before going i
Brrunno [24]

Answer: Option B

Explanation:

The glucose is the basic unit of energy. It is absorbed by the cells of the body. The glucose that is taken inside the body by the means of food is utilized to gain energy.

The glucose that is absorbed from the food moves to interstitial spaces before going inside the cell.

100% of the glucose is transferred from the interstitial spaces of the cell to the inside of the cell.

This is because more amount of the glucose is still outside the cell as it is absorbed completely.

5 0
3 years ago
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