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Dafna11 [192]
3 years ago
10

Which type of radiation has the shortest wavelength? visible light X-rays gamma rays radio waves

Biology
2 answers:
Arlecino [84]3 years ago
8 0

Answer:

gamma rays

Explanation:

There are different types of radiations/electromagnetic waves within the electromagnetic spectrum. These include:

  • <em>radio waves</em>
  • <em>visible rays</em>
  • <em>X-rays</em>
  • <em>infra-red</em>
  • <em>ultra-violet rays</em>
  • <em>microwave</em>
  • <em>Gamma rays</em>

The order of arrangement according to their wavelength is:

<em>Gamma rays < X-rays < uv rays < visible rays < Infra-red < microwave < radio waves.</em>

Gamma rays has the shortest wavelength while radio waves has the longest wavelength.

The correct answer is gamma rays.

Svetllana [295]3 years ago
3 0
The answer is Light Waves

Light waves with shorter wavelengths (and higher frequencies) also have more energy, so types of light like gamma rays, X-rays, and ultraviolet light are more energetic than visible light, and infrared, microwaves, and radio waves are less energetic than the light in the visible spectrum.
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Answer:

a) There are lots of genes on chromosome 1 could be affected, and the gametes could be imbalanced (missing segments of DNA or whole chromosomes)

b) Roughly 50%

c) No. I would advise that the couple undergo preimplantation genetic diagnosis, so that a zygote carrying the normal copy of chromosome 1 could be selected.

Explanation:

Chromosome 1 is one of the largest and most gene rich chromosomes. An inversion that covers 70% of its length would cover lots of genes.

While an inversion on its own would not seem problematic (as all the genes on the chromosome are still there), when it comes to meiosis, the sister chromatids would not be able to correctly align, and crossing over would further complicate this. It could also lead to unbalanced gametes missing entire parts of the chromosome. Therefore, there are likely numerous genes that will be affected and messed up by the inversion.

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b) There is a 50% chance of a child inheriting the defective copy of chromosome 1 (and 50% of a chance of them inheriting the normal chromosome 1. Therefore, there is likely a 50% chance that future offspring would be affected by defects

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