What is the scientific name of Neelakuranji

Which statement explains how the fossil record supports the theory of evolution?

mr_godi [17]

It's B

Explanation:

Because the fossil record shows how organisms have evoluate from relatively simple organisms to more complex organisms

4 0

3 years ago

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Early in development, every neuron has the potential to

bazaltina [42]

Early in development, every neuron has the potential to become any type of neuron
When the neurons become mature, they will experience a differentiation process. During this process, the neurons will produce several <span>subpopulations that could only be fit to certain parts of our nervous system.</span>

8 0

3 years ago

What part(s) of the cell cycle is (are) most likely being affected by cancer ?

BARSIC [14]

Answer:

DNA Synthesis the number of chromosomes is altered so that there are either too many or too few chromosomes in the cells.

Explanation:

4 0

2 years ago

In Drosophila, the genes for withered wings (whd), smooth abdomen (sm) and speck body (sp) are located on chromosome 2 and are s

lesya692 [45]

Answer:

A) 47; B) 33; C) 272; D) 122

Explanation:

The three genes are linked.

The female with withered wings and a smooth abdomen has the genotype whd sm sp+/whd sm sp+.

The male with a speck body has the genotype whd+ sm+ sp/whd+ sm+ sp.

Both individuals are homozygous for all genes, so each of them only produces one type of gamete. The resulting F1 therefore has the genotype whd sm sp+/ whd+ sm+ sp, heterozygous for all genes and with a wild-type phenotype.

The females of the F1 were mated with homozygous recessive males (test cross): whd sm sp/whd sm sp.

If we assume interference is 0, the probability of crossing over happening between the genes whd and sm is independent from the probability of crossing over happening between sm and sp.

The distance = frequency of recombination × 100, so the frequency of recombination (RF) between genes whd and sm is 0.305 and the RF between genes sm and sp is 0.155.

<u>The expected double crossover progeny among the 1000 offspring will be:</u>

RF whd-sm × RF sm-sp × 1000 =

0.305 × 0.155 × 1000 = 47 individuals will be double crossover.

Interference is 0.3

The interference is calculated as 1- coefficient of coincidence (cc).

cc = observed double crossover/expected double crossover

Therefore:

I = 1 - cc

cc = 1 - I

Observed DCO / 47 = 0.7

Observed DCO = 0.7 × 47

Observed DCO ≅ 33

The parental gametes are whd sm sp+ and whd+ sm+ sp (the genotype of the F1 female is known).

Looking at them and at the gene map we can tell that the gametes that give rise to withered wings, speck body (whd sm+ sp) and smooth abdomen (whd+ sm sp+) phenotypes are the result of recombination occurring between genes whd and sm.

To calculate the expected number of individuals with those phenotypes among the 1000 progeny we need to determine the frequency of recombination between the genes whd and sm considering there's interference.

The distance whd-sm = RF x 100

The recombination frequency is the sum of the single crossover between whd and sm and the double crossovers.

The frequency of DCO is 33/1000=0.033.

Distance whd-sm/ 100 = SCOwhd-sm + DCO

0.305 - 0.033 = SCO whd-sm

<u>Frequency of SCO whd-sm= 0.272</u>

And the expected number of individuals with those phenotypes will be 0.272 x 1000 = 272.

The gametes that originate the phenotypes withered wings, speck body, smooth abdomen (whd sm sp) and wild type (whd+ sm+ sp+) are the result of recombination between genes sm and sp.

Distance sm-sp/ 100 = SCOsm-sp + DCO

0.155 - 0.033 = SCOsm-sp

<u>Frequency of SCO sm-sp= 0.122</u>

And the expected number of individuals with those phenotypes will be 0.122 x 1000 = 122.

6 0

3 years ago

What are some possible consequences of a mutation? Give a specific example for each consequence you list.

Tju [1.3M]

Since all cells in our body contain DNA, there are lots of places for mutations to occur; however, some mutations cannot be passed on to offspring and do not matter for evolution. Somatic mutations<span> occur in non-reproductive cells and won't be passed onto offspring. For example, the golden color on half of this Red Delicious apple was caused by a somatic mutation. Its seeds will not carry the mutation.
</span>

A single germ line mutation can have a range of effects:

<span><span>No change occurs in phenotype.
Some mutations don't have any noticeable effect on the phenotype of an organism. This can happen in many situations: perhaps the mutation occurs in a stretch of DNA with no function, or perhaps the mutation occurs in a protein-coding region, but ends up not affecting the amino acid sequence of the protein.</span><span>Small change occurs in phenotype.
A single mutation caused this cat's ears to curl backwards slightly.</span><span>Big change occurs in phenotype.
Some really important phenotypic changes, like DDT resistance in insects are sometimes caused by single mutations. A single mutation can also have strong negative effects for the organism. Mutations that cause the death of an organism are called lethals — and it doesn't get more negative than that.</span></span>

4 0

3 years ago

What is the scientific name of Neelakuranji​

What is the scientific name of Neelakuranji