Answer:
Excretion is a process by which metabolic waste is eliminated from an organism.
Answer:
(a) crossing over: Meiosis I, Recombination
(b) chromatids separate at their centromeres and migrate to opposite poles: Meiosis II, Anaphase II
(c) chromosomes become aligned in pairs at the equator: Meiosis II, Metaphase II
Explanation:
Homologous recombination is a type of genetic recombination that occurs during meiosis (formation of ovum and sperm cells). The paired chromosomes of the male and female parents are aligned so that similar DNA sequences intersect. This crossing over produces an exchange of genetic material, which is an important cause of the genetic variability observed in the offspring.
Meiosis II: Anaphase II. The centromeres separate and the daughter chromatids - now individual chromosomes - move to the opposite poles of the cell. The centromeres separate, and the two chromatids of each chromosome move toward the opposite poles in the spindle.
Meiosis II: Metaphase II. Chromosomes are accommodated in the equatorial plate of metaphase, similar to what happens in mitosis. They are attached to the already fully formed meiotic spindle. Each chromosome is aligned in the equatorial plate of the metaphase, as it happens in mitosis.
The answer is: sustained (or extended) release preparation.
<span>A sustained-release medication is a drug whose release of the active ingredient is controlled over time, that is to say, that it diffuses more slowly and longer in the body.
</span>These medications can be any type of preparation, it could be tablets, capsules, ophthalmic or dermal insert, suppository...
Answer:
streak, pour
Explanation:
The streak method is the most popular technique used to isolate specific bacteria from a sample containing different microorganisms. In this technique, a sterile loop is employed to obtain an uncontaminated microbial culture. Colony picking refers to the process where colonies of pure bacteria are selected in order to duplicate them by transferring them into new agar plates. Moreover, the pour plate method is the most popular technique employed to count the number of colony-forming bacteria (i.e., bacteria/ml) in a specimen. The pour plate method consists of dropping the sample on a sterile plate and subsequently molten-cooled agar is then poured into the plate and mixed well with the inoculum.