<u>Answer:</u>
- few nutrients
- high pressure
- low temperatures
<u>Explanation:</u>
1. Few nutrients: open-ocean zone is located way far from the land, which is the main source of the essential nutrients.
2. High pressure: pressure increases by 1 atmosphere for every 10 meters increase in depth.
3. Ample sunlight: a large fraction of the sunlight is reflected back to the atmosphere from the sea surface.
4. Varying salinity: below the thermocline, the water is isolated from the atmosphere so the salinity remains stable over the year.
5. Low temperatures: the temperature of open-ocean zone ranges from a low of -2°C to an average of 17°C.
The correct answer is C. To block UV radiation. Ozone filters the majority of UV spectra, so it protects organisms from its effects.
I got you :)
The molecular clock (based on the molecular clock hypothesis (MCH)) is a technique in molecular evolution that uses fossil constraints and rates of molecular change to deduce the time in geologic history when two species or other taxa diverged. It is used to estimate the time of occurrence of events called speciation or radiation. The molecular data used for such calculations is usually nucleotide sequences for DNA or amino acid sequences for proteins. It is sometimes called a gene clock or evolutionary clock.
The technology that was used to produce the results illustrated in the image is gel electrophoresis and it is used for separating deoxyribonucleic acid (DNA) fragments.
Gel electrophoresis can be defined as a technology that is used in the laboratory for the separation of mixtures of deoxyribonucleic acid (DNA), ribonucleic acid (RNA) or other macromolecules such as proteins based on molecular size and charge.
In gel electrophoresis, an electric current is applied to the deoxyribonucleic acid (DNA) samples so as to create fragments that can be used to compare the various samples of deoxyribonucleic acid (DNA).
The steps involved in gel electrophoresis include the following:
- Extraction of deoxyribonucleic acid (DNA).
- DNA isolation and amplification.
- Addition of deoxyribonucleic acid (DNA) to the gel wells.
- Application of an electric current to the gel.
- The separation of DNA bands based on molecular size and charge.
- Deoxyribonucleic acid (DNA) bands are stained.
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