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klasskru [66]
2 years ago
5

Which is an area located within the alpine tundra? A. Sonoran Desert B. Amazon Rainforest C. Himalaya Mountains D. Australian Tr

opical Savanna
Biology
1 answer:
emmasim [6.3K]2 years ago
5 0
Hey

c)Himalayas mountain

thanks
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Multiple responses. Select all of the leukocytes that are classified as granulocytes: cytoplasmic granules and lobed nuclei.
katrin [286]

Answer:

Lymphocyte ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎

︎

︎ ︎ ︎︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎ ︎

︎

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3 years ago
What are some facts about animal cells?
Masteriza [31]
Animal cells dont have a cell wall like plant cells 
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2 years ago
The following F2 phenotypic data was obtained from a Drosophila testcross using an F1 offspring. Assume red eye and brown body a
dmitriy555 [2]

Answer:

The genotype of the F1 was wy+/w+y.

Explanation:

One of the given options has a typo: the red eye-brown body offspring count should be 56 instead of 561.

<u>We have two genes with two alleles each:</u>

Red eyes (w+) is dominant over white eyes (w).

Brown body (y+) is dominant over yellow body (y).

The phenotypes of the F2 tesulting from a test cross (F1 x wy/wy) are:

  • wy+/ey (white-eye, brown body): 670
  • w+y/wy (red-eye, yellow body): 650
  • wy/wy (white-eye, yellow body): 38
  • w+y+/wy (red-eye, brown body 56

If the genes w and y are linked, two phenotypes in the F2 will be much more abundant than the other two. Recombination during meiosis is a rare event, so the most abundant phenotypes are the parentals (the ones present in the F1 parent).

Every individual in the offpsring has a <em>wy</em> chromosome, as this was the gamete inherited from the test cross individual.

In this case, the most abundant gametes are wy+ and w+y, so the genotype of the F1 was wy+/w+y.

Notice how when recombination occurs in the F1 parent, the recombinant gametes appear: wy and w+y+, which are the less abundant in the F2 progeny.

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3 years ago
I rEALLY nEeD THiS AnSWeR sO bAD
Ilia_Sergeevich [38]

the answer is the third one c

7 0
3 years ago
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How is coffin-lowry syndrome inherited? Do both parents need to have the disorder in order for their child to have it?
svp [43]

Answer:

Explanation:

Coffin-Lowry syndrome is caused by changes (mutations) in the RPS6KA3 gene and is inherited in an X-linked dominant pattern. Males are usually more severely affected than females.

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