It's kinda hard to read can you put another pic or something?
Bacteriophages most frequently have which sort of morphology, when bacterial genes are transmitted from one bacterium to another by a virus.
<h3>What does a bacteriophage look like morphologically?</h3>
The best method for examining the morphology of bacteriophages is electron microscopy. It has a polyhedral head, a short neck and collar, and a straight tail. It is tadpole-shaped. The head is 950 x 650 in size and has a bipyramidal hexagonal form. A membrane (capsid) that is about 35 thick encloses the contents of the head.
<h3>What kind of bacteriophage is most typical?</h3>
Assphages are a large and common family of tailed bacteriophages that are thought to infect bacteria belonging to the phylum Bacteroidales. Members of this viral family have never been isolated in culture and are still poorly understood despite being present in up to 50% of people and accounting for up to 90% of human gut viromes.
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Answer:
<h3>Seafloor sediment consist mostly of terrigenous sediment, biogenous sediment and hydrogenous sediment. Terrigenous sediments form from sediments carried from the land into the ocean by water, wind or ice.</h3>
Ok, so I wrote these out just to make it a little bit easier for you to understand what I am about to explain.
So for the first one you have two different traits that can be inherited- having freckles or having no freckles, F and f respectively. The dominant trait (or having freckles) is shown by the capital F, and is almost always expressed over the recessive trait, or the lowercase f. So, for example, if you have a genotype of Ff, the trait having freckles will show up instead of not having freckles. The only way that you could have the trait of no freckles show up is if there are two recessive alleles for having no freckles, or ff. In this case, you have two parents who are both heterozygous for the trait of having freckles, so in other words the mother has Ff and the father has Ff. Each parent passes down one allele to the offspring, so since you are breeding Ff and Ff, you should result in having the possible genotypes of FF, Ff, Ff, and ff. This means that there is a 25% chance that the offspring will be homozygous for having freckles, a 50% chance that the offspring will be heterozygous for having freckles and a 25% chance that they would be homozygous for having no freckles, or a 1:2:1 ratio.
Incomplete dominance is a little bit different that just a normal monohybrid cross. Instead of just the dominant gene showing up in a heterozygous genotype, both traits show up. So like the question says, if a homozygous red flower plant was crossed with a homozygous white flower plant, their offspring would not just be white or red, they would be pink because it is a mixture of white and red. So then if you crossed the heterozygous, or Rr plants, the result would be a 25% chance of getting a homozygous RR red plant, a 50% chance of getting a pink Rr plant, and a 25% chance of getting a white rr plant, or another 1:2:1 ratio.
Sorry for the wordy answer, but hopefully this helps you understand this a little better :)