It is called an autotroph.
Answer:
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Explanation:
The ocean plays an important part in the carbon cycle.
- Overall, the ocean is called a carbon 'sink' because it takes up more carbon from the atmosphere than it gives up.
- Photosynthesis by tiny marine plants (phytoplankton) in the sunlit surface waters turns the carbon into organic matter.
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Answer:
<u> The following four traits are -: </u>
- <u>Pedigree 1 -</u> A recessive trait (autosomal recessive) is expressed by pedigree 1.
- <u>Pedigree 2- Recessive inheritance is defined by Pedigree 2. </u>
- <u>Pedigree 3</u> - The inheritance of the dominant trait (autosomal dominant) is illustrated by Pedigree 3.
- <u>Pedigree 4-</u> An X-like dominant trait is expressed by Pedigree 4.
Explanation:
<u>Explaination of each pedigree chart</u>-
- Pedigree 1 demonstrates the <u>recessive trait </u>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. In this, both parents are autosomal recessive trait carriers, so the child will be affected by a 1/4 (aa)
- <u> Recessive inheritance</u> is defined by <u>Pedigree 2</u>. This is<u> X-related inheritance as autosomal recessive</u> 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 1/2 (probability of Y from father II-6) = 1/8. An affected daughter's likelihood is 0 because a typical must be contributed by II-6.
- The inheritance of the<u> dominant trait</u> is demonstrated by <u>Pedigree 3 </u>because affected children still have affected parents (remember that all four diseases are rare). The trait must be <u>autosomal dominant</u> 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.
- <u>Pedigree 4</u> is an <u>X-linked dominant function</u> 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.
Answer:
Answer is D, all of the above.
Answer:
Transition
Explanation:
Secondary succession occurs when the existing vegetation is removed by some disturbances and soil is already present in the region to support the growth of new species. During succession, the early species are being replaced by later successional species.
In the given example, the forest has patches of early species and later species. This means that the forest is in the transition period of succession where early species were not completely replaced by the new species. Once the early species will be removed and the climax community develops, the forest has reached the final stage of succession.