HURRY

2 answers:

muminat3 years ago

8 0

the answer to this is D because these rays can show you where the fire is located even if it is enveloped in a cloud of gray of black smoke that prevents you from seeing it.

const2013 [10]3 years ago

7 0

D. Infrared images can show hot spots as red areas.

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Each of the four pedigrees that follow represents a human family within which a genetic disease is segregating. Affected individ

Ne4ueva [31]

Answer:

The following four traits are -:

Pedigree 1 - A recessive trait (autosomal recessive) is expressed by pedigree 1.
Pedigree 2- Recessive inheritance is defined by Pedigree 2.
Pedigree 3 - The inheritance of the dominant trait (autosomal dominant) is illustrated by Pedigree 3.
Pedigree 4- An X-like dominant trait is expressed by Pedigree 4.

Explanation:

Explaination of each pedigree chart-

Pedigree 1 demonstrates the recessive trait since their children have been affected by two unaffected individuals. If the characteristics were X-linked, in order to have an affected daughter, I-1 would have to be affected. $X^A$ In this, both parents are autosomal recessive trait carriers, so the child will be affected by a 1/4 (aa)
Recessive inheritance is defined by Pedigree 2. This is X-related inheritance as autosomal recessive inheritance has already been accounted for in part 1. This inference is confirmed by evidence showing that the father (I-1) is unaffected and that only the sons exhibit the characteristic in generation II, suggesting that the mother must be the carrier. The individual I-2 is a carrier for this X-linked trait. A typical Xa chromosome is attached to the unaffected father (I-1), so the chance of carrier II-5 is 1/2. Probability of an affected son = 1/2 (probability II-5 is a carrier) x 1/2 (probability II -5 contributes ( $X^A$ ) x 1/2 (probability of Y from father II-6) = 1/8. An affected daughter's likelihood is 0 because a typical $X^A$ must be contributed by II-6.
The inheritance of the dominant trait is demonstrated by Pedigree 3 because affected children still have affected parents (remember that all four diseases are rare). The trait must be autosomal dominant because it is passed down to the son by the affected father. There is a 1/2 risk that the heterozygous mother (II-5) would pass on mutant alleles to a child of either sex for an autosomal dominant feature.
Pedigree 4 is an X-linked dominant function characterized by the transmission to all of his daughters from the affected father but none of his son. On the mutant X chromosome, the father (I-1) passes on to all his daughters and none of his sons. As seen by his normal phenotype, II-6 therefore does not bear the mutation. An affected child's likelihood is 0.

In the question the pedigree chart was missing ,hence it is given below.

7 0

3 years ago

Please help !!!!!!!!!

algol13

The biosphere. This is the layer that contains all life on the planet.

3 0

3 years ago

Read 2 more answers

Disruptive selection events select for _______. a. common traits b. genetic uniformity c. camouflage traits d. extreme traits

Gelneren [198K]

D extreme traits is ur answer

6 0

3 years ago

Biogeochemical system

Dovator [93]

Answer:

Explanation:

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5 0

3 years ago

Which is a limitation of a scientific model?

iren [92.7K]

Answer:

The correct option is D) Models are not the "real thing" so it will never correctly represent the system in all respects.

Explanation:

Scientific modelling can be described as a representation of the scientific theories or concepts in a way that can be better understood. Scientific models makes it easier to understand what physical, chemical or mechanical activity is taking place. Even mathematical representation comes under scientific modelling.

As models are not the real, hence they cannot be considered to be perfectly accurate. A model can never mark up to the complexity of nature.

8 0

3 years ago