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likoan [24]
3 years ago
11

What is the role of a producer?

Biology
2 answers:
Stells [14]3 years ago
7 0

Answer:

the answer is D because it gets energy from the sun and then gives it off to the primary consumer when it eats it

Elodia [21]3 years ago
4 0
The answer is B it provides energy to decomposers
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Select the statements that best explain Makali's GALT activity levels? Makali may have a mutation in the gene that encodes galac
adelina 88 [10]

Answer:

Makali may produce only small amounts of a non-mutated (wild-type) GALT enzyme.

Makali may have normal amounts of GALT, but the enzyme may be mutated.

Explanation:

Makali is lactose intolerant because of his ancestry. Because of this he is not able to digest any lactose which indirectly protected him from galactosemia. Thus he must avoid consuming galactose. He has a low GALT or galactose 1‑phosphate uridylyltransferase activity. He has a normal amount of GALT and may produce only small amounts.  

4 0
3 years ago
Select all that apply. Choose the cells that are diploid. egg nerve bone sperm muscle
Natali5045456 [20]
The diploid cells in this case include nerve cell, bone cell and muscle cell. A diploid cell is a cell that contains two sets of chromosomes, which is double the haploid chromosome number. They include all the somatic cells with exception of germ line cells. Gametes are haploid cells meaning they only have one set of chromosomes. During sexual reproduction, gametes (sperm and egg cells) fuse at fertilization to form a diploid zygote which develops into a diploid organism.
8 0
2 years ago
Read 2 more answers
Qué tipo de anomalía cromosómica es el síndrome de down y Cómo se manifiesta? ¿Qué tipo de anomalía cromosómica es el síndrome d
sashaice [31]

Answer:

El síndrome de Down es el resultado de un niño nacido con un cromosoma adicional agregado al número esperado de cromosomas (generalmente destinado a ser 46).

El síndrome de Angelman se produce cuando un niño nace con una mutación en el 15º cromosoma heredado de los padres.

Explanation:

En el síndrome de Down, se agrega un cromosoma adicional al complemento de cromosomas que un niño debe heredar de sus padres. Se supone que un niño tiene un complemento de 46 cromosomas (23 cada uno) de ambos padres. Una vez que hay un aumento en este número, se establece el síndrome de down. Es una condición cromosómica común. Puede manifestarse como una trisomía, causada por la no disyunción durante la división celular, lo que resulta en 3 copias del cromosoma 21 en lugar de 2 copias, mosaicismo, donde una mezcla de células se clasifican en 2 grupos que contienen un complemento completo de 46 cromosomas y el otro un el cromosoma adicional lo hace 47 y la translocación ocurre cuando un cromosoma 21 adicional o parte del 21 se une al cromosoma 14. Los niños generalmente tienen cabezas y orejas pequeñas, cuellos cortos, caras planas, etc.

En el síndrome de Angelman, el cerebro se ve afectado en gran medida, debido al efecto de la mutación en el sistema nervioso. La pérdida de la función en el 15º cromosoma es responsable del síndrome de Angelman, que resulta en la incapacidad del niño para hablar, mantener el equilibrio, moverse, un desarrollo deficiente tanto física como intelectualmente.

5 0
2 years ago
Help me what’s the answer
Kazeer [188]
The answer i believe is “c”
5 0
3 years ago
In a hydrogen ion pump, the energy is used to join small molecules together to make larger ones. Which factor most likely has th
Pani-rosa [81]
All the options are incorrect. The correct answer will be THE NUMBER OF HYDROGEN IONS MOVING DOWN THE PROTEIN CHANNEL.

A proton pump is found in the inner membrane of mitochondria which is also known as hydrogen ion pump. The hydrogen ion is pumped across the inner mitochondrial membrane depending on the proton gradient.


6 0
2 years ago
Read 2 more answers
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