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Stella [2.4K]
3 years ago
12

Which is in Phylum Nematoda? A. Planarian B. Earthworms C. Nematode D. Tapeworm

Biology
1 answer:
oksano4ka [1.4K]3 years ago
5 0
Species in the phylum Nematoda (from the Greek root word nema meaning thread) are better known as the roundworms
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Use what you know about natural selection to fill in the blanks in the hypothesis. It should answer the lab question, “What is t
lubasha [3.4K]

Answer:

For example, if the seeds that the bird needs to eat is bigger, over time it will adapt to get a bigger beak to eat the bigger seed. The birds that have adapted reproduce and soon more and more birds that have a bigger beak for the bigger seed are more common. If the type of food available changes than the bird will most likely adapt to eat that food.

8 0
3 years ago
What was an unexpected consequence of the green revolution?
KengaRu [80]
<span>The correct answer is a. the overuse of fertilizer lead to reduced crop yields over time. This was unexpected because it is common for fertilizers to increase the yields and the quality of the product, but what happens over time is the opposite so it can be said that it's an unexpected consequence.</span>
7 0
4 years ago
Read 2 more answers
Purple flowers are dominant to white flowers. A heterozygous purple flower is crossed with a white flower. What are the probabil
Zanzabum

Answer:

50% probability of Pp (purple) or pp (white) genotype.

Explanation:

P = purple gene

p = white gene

Punnet squares show the possible genotypes and probabilities of each genotype in the offspring of a cross:

Purple flower genotype (heterozygous) = Pp

White flower genotype = pp

Punnet Square:

\left[\begin{array}{ccc}&P&p\\p&Pp&pp\\p&Pp&pp\end{array}\right]

Potential genotypes for offspring are Pp and pp;

According to the Punnett square, 2 of 4 offspring will have the Pp genotype and the other 2 will have pp genotypes;

This means 2 should be purple and 2 white;

Or, there is a 50% chance of having either genotype, of being purple or white.

8 0
3 years ago
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Prader-Willi syndrome is a genetic disorder involving a partial deletion of chromosome 15q on the paternal chromosome. When both
Kay [80]

Answer:

genomic imprinting

Explanation:

Genomic imprinting is a mechanism for regulating gene expression that allows expression of only one of the parental alleles, although both alleles are functional. Unlike most genes in which expression is biallelic, genes that are subjected to this mechanism (imprinted genes) have monoalelic expression; By definition, in an imprinted loci, only one allele is active (maternal or paternal), and the inactive is epigenetically marked by histonic modification and / or methylation of cytosines.

Genomic imprinting can cause some disturbances, among them Prader-Willi syndrome, which is a genetic disorder that involves a partial deletion of chromosome 15q on the paternal chromosome.

3 0
3 years ago
What role do variations have in the theory of evolution by natural selection?
Black_prince [1.1K]

Answer:

Individuals in a population are naturally variable, meaning that they are all different in some ways. This variation means that some individuals have traits better suited to the environment than others. ... Through this process of natural selection, favorable traits are transmitted through generations.

3 0
3 years ago
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