Which of these would most likely happen if there is a sudden increase in the number of sunspots?A. summers would become colder
B. Earth's tilt on its axis would decrease
C. Earth's climate would become warmer
D. length of days and nights would increase

Answers

Answer 1
Answer:

Which of these would most likely happen if there is a sudden increase in the number of sunspots?

C. Earth's climate would become warmer

The correct answer is option C.

The sudden increase in sunspots will make the Earth more warmer because the more the sunspots, more energy is delivered to the atmosphere. This increases the global temperatures of the Earth.

Answer 2
Answer:

Answer:

The correct answer is C.

Explanation:

Sunspots increase and decrease through an average cycle of eleven years.

There is a debate of how much this sunspot would affect the earth`s temperature, the earth`s climate is sensitive to very weak changes in the Sun`s energy. During maximum sunspot activity, there`s a very slight increase in the energy output of the sun. Ultraviolet radiation increases during high sunspot activity, and this can have a large effect on Earth`s atmosphere.

I hope it helps!


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Mutations that arepassed to offspring must occur

Why does an insertion mutation usually cause more defects during protein synthesis than a point mutation?a. insertion mutations only occur during transcription.
b. insertion mutations can only be silent mutations.
c. insertion mutations can affect many amino acids in the protein.
d. insertion mutations are chromosomal mutations?

Answers

The study of cells is called cell biology. There are two types of a cell on the basis of their number and these are unicellular and multicellular.

The correct answer to the question is option C that is insertion mutations can affect many amino acids in the protein.

What is transcription?

  • The conversation or transferring of the gene from DNA to RNA is called transcription.

What is mutation?

  • The abnormality in the gene in the DNA sequence which forms a mutated protein is called a mutation.

The formation of protein is called translation. This addition of genes changes the sequence of RNA which alters the protein formation while in point mutation it changes only one amino acid.

Hence, the correct answer is option C.

For more information about the transcription, refer to the link:-

brainly.com/question/15209553

Please help ! I’ll mark brainliest

Answers

Answer:

the sun

Explanation:

_______ is a very old drug that's used subcutaneously to prevent DVT in high-risk patients and intravenously to treat DVT and PE. A. Heparin B. Warfarin C. Pradaxa D. Xarelto

Answers

The correct answer is the option (A) heparin.

DVT refers to a condition called the deep vein thrombosis when a blood clot occurs in the deep veins of the legs in the body. PE refers to the Pulmonary embolism when a blood clot is observed in the artery of the lungs.

The drugs used in the treatment of DVT and PE are called the anticogulants which interfere with the process of blood clot formation. Heparin and warfarin are the two older anticoagulants used in the prevention and treatment and prevention of DVT and PE. Heparin is given intravenously to treat DVT and PE whereas, warfarin is taken as a tablet or pill through the mouth. Heparin allows the body's clot lysis mechanism to break down the existing clots and it is also a natural anticoagulant produced by the basophils and the mast cells of the blood.

Thus, heparin is the old drug that is used subcutaneously to prevent DVT in high-risk patients and intravenously to treat DVT and PE.

Original DNA coding strand: TAC CCG ACG GGC GAT AGT TTCDNA 1: TAC CCA CGG GCG ATA GTT TC

DNA 2: TAC CCG ACG GGC GAT AGT TTT

a) What types of mutation have occurred in each of the DNA 1 and DNA 2 sequences?
b) Explain how these mutations affect the amino acid sequence produced and the overall effect on the final protein. Which mutation will cause the most disruption to the overall protein structure and why?

Answers

A) DNA 1 by chromosomal mutation
DNA 2 by genetic mutation



Hope it’s usefullll

Tail length in mammals is a heritable trait. A pig with a 6 cm tail was mated to a pig with a 30 cm tail. All F1 offspring had a tail of length 18 cm. An F2 generation was made by crossing F1 individuals. This resulted in many piglets whose tails ranged in 4-cm intervals from 6 to 30 cm (6, 10, 14, 18, 22, 26, 30). The majority of pigs had 18 cm tails, 1/64 had 6 cm tails, and 1/64 had 30 cm tails.These results are consistent with what genetic model?

(a) Two genes, each with two alleles that show dominance
(b) Two genes, each with two alleles that act additively
(c) Three genes, each with two alleles that show dominance
(d) Three genes, each with two alleles that act additively

An F2 piglet with an 18 cm tail is heterozygous at each of the tail-length loci, and is mated to an F2 piglet with a 6 cm tail. Write down the predicted offspring genotypes and calculate the predicted tail lengths. What is the expected frequency of piglets with a 14 cm tail length?

Answers

Answer:

The answer is (d) Three genes, each with two alleles that act additively.

Explanation:

1/ The genotype of P is AABBCC and aabbcc, for example. Then, F1 should be AaBbCc.

The genotype of individuals with n heterozygous pair is 2^n. Thus, in this case, the number of genotype in F2 should be 2^3 * 2^3 = 8 * 8 = 64. We can get this conclusion by analyzing the number of 6 cm tails in F2: 1/64 with genotype aabbcc, and the number of 30 cm tails: 1/64 with genotype AABBCC. These two genotypes is as same as the ancestor in this experiment.

The genotype of an F2 piglet with an 18 cm tail is AaBbCc. If these genes show dominance, the tail lenght of F2 will be 30 cm. And there are 7 possible phenotypes. Thus, we can conclude that the genes act additively.

2/ 18 cm tail F2: AaBbCc, and 6 cm tail: aabbcc.

The offspring genotypes are:

  • 18 cm AaBbCc, 14 cm AaBbcc, 14 cm AabbCc, 10 cm Aabbcc
  • 14 cm aaBbCc, 10 cm aaBbcc, 10 cm aabbCc, 6 cm aabbcc

The frequency of piglets with 14 cm tail length should be 3/8 = 37.5%.

Answer and Explanation:

1) These results are consistent with option (d)Three genes, each with two alleles that act additively .

Quantitative heritability: Refers to the transmission of a phenotypic trait in which expression depends on the additive effect of a series of genes.

Polygenic heritability occurs when a trait is due to the action of more than one gene that can also have more than two alleles. This can cause many different combinations that are the reason for genotypic graduation.

Quantitative traits are those that can be measure, such as longitude, weight, eggs laid per female, among others. These characters do not group individuals by precise and clear categories. Instead, they group individuals in many different categories that depend on how the genes were intercrossed and distributed during meiosis. The result depends on how each allele of each gene contributed to the final phenotype and genotype.

In the exposed example, there are 7 different phenotypes  (6, 10, 14, 18, 22, 26, 30) and the majority of F2 individuals have 18-lengthed tails. This might be the heterozygotic phenotype for all the genes.The rest of the phenotypes are possible combinations of genes and their alleles. There are six possible combinations (apart from the 18 lenght form). This leads to 3 genes and two alleles in each gene.

So, until now we have:

  • A pig with a 6 cm tail was mated to a pig with a 30 cm tail. All F1 offspring had a tail of length 18 cm. This is:

Parental)     6cm    x    30cm

F1)                       18 cm  

  • An F2 generation was made by crossing F1 individuals. This resulted in many piglets whose tails ranged in 4-cm intervals from 6 to 30 cm (6, 10, 14, 18, 22, 26, 30). This is:

Parental)       18 cm   x   18 cm

F2)               6, 10, 14, 18, 22, 26, 30

  • The majority of pigs had 18 cm tails, this means that 18 cm phenotype is a heterozygote for each gene
  • 1/64 had 6 cm tails, and 1/64 had 30 cm tails, this means that these two phenotypes are the extreme traits, that is the recessive homozygote and the dominant homozygote.
  • There are 7 phenotypes, one of them is the recessive form, the other is the dominant form and the majority is the heterozygotic form for every intervening gene. There are three genes with two alleles each:

Gene 1: allele A and a

Gene 2: allele B and b

Gene 3: Allele C and c

Phenotypes:

aabbcc: homozygotic recessive form

AABBCC: homozygotic dominant form

AaBbCc: heterozygotic form for every intervening gene

If the recessive form is 6cm length, and each dominant allele contributes in 4 cm to each phenotype, we get:  

  • 6 cm length = aabbcc (1/64)
  • 10cm length = Aabbcc  (A contributes 4cm)
  • 14cm length = AaBbcc  (A and B contribute 4 cm each)
  • 18cm length = AaBbCc (The majority) (A, B and C contribute 4cm each)
  • 22cm length = AABbCc
  • 26cm length = AABBCc
  • 30cm length = AABBCC (1/64)

2) An F2 piglet with an 18 cm tail is heterozygous at each of the tail-length loci, and is mated to an F2 piglet with a 6 cm tail.  

Parental)       AaBbCc     x     aabbcc

Gametes)   ABC  ABc  AbC  Abc  aBC  aBc  abC  abc

                  abc   abc   abc   abc   abc   abc  abc  abc

Punnet square)  

            ABC        ABc       AbC       Abc      aBC       aBc        abC      abc

abc    AaBbCc AaBbcc AabbCc Aabbcc aaBbCc aaBbcc aabbCc aabbcc  

abc    AaBbCc AaBbcc AabbCc Aabbcc aaBbCc aaBbcc aabbCc aabbcc

abc   AaBbCc AaBbcc AabbCc Aabbcc aaBbCc aaBbcc aabbCc aabbcc

abc    AaBbCc AaBbcc AabbCc Aabbcc aaBbCc aaBbcc aabbCc aabbcc          

abc    AaBbCc AaBbcc AabbCc Aabbcc aaBbCc aaBbcc aabbCc aabbcc          

abc    AaBbCc AaBbcc AabbCc Aabbcc aaBbCc aaBbcc aabbCc aabbcc          

abc    AaBbCc AaBbcc AabbCc Aabbcc aaBbCc aaBbcc aabbCc aabbcc      

abc    AaBbCc AaBbcc AabbCc Aabbcc aaBbCc aaBbcc aabbCc aabbcc          

F3 genotype and phenotype)

8/64 AaBbCc = 18 cm

8/64 AaBbcc = 14cm

8/64 AabbCc = 14cm

8/64 Aabbcc = 10cm

8/64 aaBbCc = 14cm

8/64 aaBbcc = 10cm

8/64 aabbCc = 10cm

8/64 aabbcc = 6cm  

Each dominant allele contributes 4cm to the recessive homozygote form for each phenotype.                                            

Which of the following contribute(s) to the variation in offspring produced by sexual reproduction? A. Crossing over
B. Mutation
C. Independent assortment
D. Random fertilization
E. All of the above

Answers

Answer:

The correct answer is E. All of the above

Explanation:

Variation in offspring can be contributed by many different events that change the DNA sequence in gametic cells. These events are crossing over, mutation, independent assortment, and random fertilization.

During the gamete formation, the different genes are assorted independently from the other gametes which results in forming various possible combinations of genes in a gamete increasing the genetic variation.

Crossing over occurs during meiosis between the homologous chromosome that results in exchange of genetic material that brings genetic variation in gametes. During random fertilization, the two gametes fuse and genetic material of two different individual comes to make an offspring which forms a genetical different offspring.

Mutation in the gametic cell is transferred to the offspring during fertilization. Therefore all contributes to variation in offspring produced by sexual reproduction.