Answer:
In contrast, applied science or “technology,” aims to use science to solve real-world problems, making it possible, for example, to improve a crop yield, find a cure for a particular disease, or save animals threatened by a natural disaster. In applied science, the problem is usually defined for the researcher.
Explanation:
I hope this helps, but when you use this make sure you copy and paste this to paraphrasing tool.
Characteristic of the Vessel elements of Angiosperms
Answer:
When we talk about the inheritance of traits, or the passage of traits from parents to future generations down the line, we are not just talking about the visual (phenotypical) expression of those traits, but also, their underlying explanation, which is the genotype. A genotype is basically how the genes of the parents combine in such a way that the children inherit a set of traits from the parents, and express them phenotypically, or not.
In the case of blood types, we have four phenotypic groups: A, B and O. Each one of these types is characterized by the underlying set of genes that are responsible for what is expressed. While the O blood type presents a genotype ii, which is recessive, the A and B types will have the following genetic patterns: Ia Ia, or, Ia i (characteristic of the O genetic material) for the A type and: Ib Ib, or Ib i, for the B type. When there is a genetic conjugation from parents genetic material, regarding blood type, we would have these sets of genes combining. In most of the possible combinations genetically speaking, we have the recessive i gene appearing, including in the A and B dominant blood types. This means that when crossed, there will always be a chance of at least one offspring presenting the O blood type, even if one of the parents is dominant A, or B.
In answer: it is the fact that all three types present the recessive allele i, typical of the O blood type, that when pairings of genes happen between parents, the genetic characteristic of the O type may present itself in a dominant fashion, instead of the usual recessive pattern.
Explanation:
The inbreeding process, are blood crossings between relatives who have a common ancestor. Inbreeding leads to an increase in the frequency of homozygous genotypes and a decrease in the frequency of heterozygotes. We may also note that although changes in genotypic frequencies occur, no changes in allelic frequencies are observed over successive generations of self-fertilization. The main consequence of 2 individuals sharing one or more common ancestors is that they may carry replicas (identical copies) of one or more genes present in these ancestors. And if these individuals mate, they can pass on such replicas to their offspring, generating self-sibling offspring, that is, with two identical copies of the same gene that was present in these common ancestors.
I believe it would be a primary succession.. (I may be wrong)
