He will use any form of length measurement to measure the length, width, and height of the pool, use the formula V=lwh to find the volume.
Explanation:
Mutations increase variation within a population.
During the process of cell division, spontaneous changes within the genome can arise. These mutations are errors occur when copies of the DNA within the cell are made; mutations may range from small changes called single nucleotide polymorphisms, to large scale deletions, and additions which span multiple genes. There are two types:
- somatic: these only occur within certain cells, and arise from environmental factors such as UV light
- hereditary: occur within germ cells of the parent and later the fertilized egg which forms a zygote; these are present within all cells of the new organism.
Further Explanation:
During reproduction other events, such as crossing over during mitosis and meiosis, mutations lead to increases in genetic variation. This variation refers to the genetic characteristics present within a species. Mutations may be either beneficial or deleterious; they are maintained within cells, as they form new traits called alleles. Beneficial mutations may confer traits that increase the fitness of a species, along with ensuring survival by conferring a protective advantage- these phenotypic differences between organisms are called adaptations.
Sequences of DNA make up genes which can have different forms called alleles. DNA, which makes up the genotype, is transcribed into mRNA and later translated into amino acids which are linked together by rRNA to form proteins which make up the phenotype of an organism.Mutations in DNA sequences affect the corresponding mRNA and thus the protein encoded.
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Answer:
The Hypothesis is a prediction based on the theory being tested.
The evidmence can support the Hypothesis or invalidate the Hypothesis.
Explanation:
Answer:
O4) Screening tests
Explanation:
The screening test is used to make early detection of diseases in order to apply effective treatments. For example, a screening blood test enables the identification of toxins and/or drugs in the patient's system in a relatively low amount of time (generally 24 hours). This bioassay is used for the toxin determination of the effluent sample (i.e., a sample collected and analyzed to evaluate system performance) to the tested species. The screening test generally consists of applying two treatments (i.e., one effluent sample and one control).
Answer:
making hole in the same to get the new DNA into the cell
