Answer:
What is the effect of power/magnification on the frequency and size of organelles under a microscope?
Explanation:
Organelles within the cell are responsible for carrying out various functions. Some cells are more specialized than others, and may have particular organelles at a higher frequency, or showing a variation in size; sub-cellular structures become more visible at higher magnifications under the microscope.
Hypotheses:
- organelle A's frequency decreases while B's frequency increases at higher magnifications
- organelle A's size increases while B's size decreases at higher magnifications
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<em>Dependent variables: size and frequency cell organelles</em>
<em>Independent variable: power/magnification at low (x4), medium(x10) and high (x40)</em>
<em>Controlled variables: Type of organelles, microscope used, cell examined, </em>
Method:
1. Examine the organelles A and B in a cell mounted on a slide; use the fine adjustment to focus on the cell.
- Frequency: What is the average number of organelle A versus B, seen at low (x4), medium (x10) and high (x40) magnifications?
- Size: Measure the average diameter of organelle A versus B using an ocular micrometer at low, medium and high magnification.
2. Record and tabulate observations.
Answer:
Basically enzyme activities are affected by drop in temperature. in additions the corpse was cool to touch.Therefore this explains while there was no bloating or bacteria activity since the decomposing bacteria enzymes were inactive because of the cold temperature.
Consequently, if the Livor mortis (lividity) is +8hrs 0-4days, evidently the corpse must have been refrigerated after livor mortis sets in, with the decomposition slowed down by the cold environment.
Notes: Algor mortis is 26.8hrs, and there was no algor mortis.
Explanation:
It doesn't do much during Interphase, it simply does it's regular functions.
Answer:
Velocity
Explanation:
Given the change in positive (direction) over time we are given the velocity formula.
V = Change in direction/Change in time
Since we are given a direction we can rule out speed as well as direction in itself. We can also rule out acceleration because that is the change in Velocity divided by change in time.
Answer:
Well protines come in diffrent shapes, for there diffrent functions. The first level, or primary structure, is the linear sequence of amino acids that creates the peptide chain. In the secondary structure, hydrogen bonding between different amino acids creates a three-dimensional geometry like an alpha helix or pleated sheet. An alpha helix is simply a spiral or coiled molecule, whereas a pleated sheet looks like a ribbon with regular peaks and valleys as part of the fabric. The tertiary structure describes the overall shape of the protein. Most tertiary structures are either globular or fibrous. Generally, nonstructural proteins such as enzymes are globular, which means they look spherical. The enzyme amylase is a good example of a globular protein. Structural proteins are typically long and thin, and hence the name, fibrous. Quaternary structures describe the protein's appearance when a protein is composed of two or more polypeptide chains. Often the polypeptide chains will hydrogen bond with each other in unique patterns to create the desired protein configuration.
some hormones are proteins; and some proteins are involved with digestion, respiration, reproduction, and even normal vision, just to mention a few.
f the three-dimensional structure of the protein is altered because of a change in the structure of the amino acids, the protein becomes denatured and does not perform its function as expected.
Explanation:
