Answer:
Consumers supply oxygen for producers to undergo aerobic respiration. Consumers produce carbon dioxide for producers to use during photosynthesis.
Consumers provide chemical energy needed by producers for cellular respiration.
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Which of the following are examples of asexual reproduction?
Select all that apply.
☞︎ a plece of a cactus falling to the ground, taking root
☞︎ a male and female organism producing offspring together
☞︎ a bacterial cell dividing
☞︎ a bacterial cell sharing a plasmld with a different bacterial cell
꧁Plz select all apply, thank you꧂
Meiosis occurs in a series of different phases and creates genetically unique reproductive cells.
Which process helps make meiotic cells genetically different and occurs during prophase I, but not during prophase II?
fertilization
independent assortment
crossing over
chromosome replication
Answer:
Meiosis occurs in a series of different phases and creates genetically unique reproductive cells. The process which helps make meiotic cells genetically different and occurs during prophase I, but not during prophase II, is crossing over (C). Crossing over is the exchange of genetic material between two homogenous chromosomes. It is one of the final phases of prophase I. This process is called synapsis. It occurs when the matching regions on the matching chromosomes break and then reconnect to the other chromosome .
The process that helps to make meiotic cells genetically different and occurs during prophase I is called crossing over.
Crossing over, also known as recombination, is the interchange of genetic material between non-sister chromatids of homologous chromosomes.This process (crossing over) occurs in Meiosis I, specifically during Prophase I.Crossing over during Prophase I and the independent assortment of homologous chromosomes during Metaphase I represent meiotic processes that help to increase genetic variation in gamete (sex) cells.In conclusion, the process that helps to make meiotic cells genetically different and occurs during prophase I is called crossing over.
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Do either of your diseases in part A have the same pattern of inheritance as the model of the colorblindness mutation you made? How do you know?
A picture of part A is down below
Most commonly, color blindness is inherited as a recessive trait on the X chromosome. This is known in genetics as X-linked recessive inheritance. As a result, the condition tends to affect males more often than females (8% male, 0.5% female).
Answer:
Most commonly, color blindness is inherited as a recessive trait on the X chromosome. This is known in genetics as X-linked recessive inheritance. As a result, the condition tends to affect males more often than females (8% male, 0.5% female).