INTRODUCTION
Typically, it can be said that life’s “powerhouse” is the sun. The energy from the sun is converted into oxygen and sugars from a process called photosynthesis which only occurs in photosynthetic organisms like plants. The sugars and oxygen produced by these organisms are then used by “consumers” for their chemical energy source. From this it can be assumed that the faster photosynthesis can happen, the more energy develops for living organisms to utilize.
Everything that has a color (excluding transparent and colorless matter) transmits, absorbs, and/or reflects energy from light. Plants, light most objects, reflect and absorb light. The color of an item is the wavelength of that color being reflected while all other wavelengths
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This was done for each dye. The remaining beaker was filled with 20 mL of distilled water and was used as the control variable.
2) The hole punch was used to cut 28 (7 for each beaker) leaf circles from the spinach leaves. The 28 leaf circles, or discs, were then scooped up with the spatula and placed into the syringe.
3) The experimenter’s finger was placed on the tip of the syringe while adding 10 mL of water into it. The plunger was then placed into the syringe, flipped upside down, and then pushed to remove any air bubbles. The finger was then replaced on the tip of the syringe, the plunger was pulled back to create a vacuum and was then released (Patterson Lab Manual 12-3). This process was repeated three times for accuracy to make sure that no leaf disks were still floating (Patterson Lab Manual 12-3). This step in the experiment was performed in order to deoxygenate the leaf circles.
4) 7 leaf disks for each 50 mL beaker were isolated from the syringe with a spatula. All 28 circles were inserted into the four beakers (7 in each) at the same time. The stopwatch was then started to record the time elapsed in between each disk
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There was 20 mL of liquid in each beaker. All leaf circles were de-oxygenated in the same way, in the same syringe, at the same time. Every beaker contained 7 leaf disks. All leaf disks were dropped into the beakers and placed under the desk lamp simultaneously. The same desk lamp was used for every beaker. The stopwatch was started at the same time for every beaker and it was used throughout the entire experiment without being stopped. All of these unchanging constants accounted for bias and control of only changing the independent variable (the different light wavelengths within the beakers) within the experiment, validating the
Experiment 1 (Assignment 3): Using sciccors, leaves from the Geranium plant were cut (Plant A was the bigger leaf and Plant B was the smaller leaf). Then begin to heat up the hot plate to boiling temperature of 100℃. Next one beaker was filled with ⅔ of water and another beaker was filled with ⅓ alcohol. Place the beaker of water onto the hot plate until boiling. To speed up the boiling process put boiling chips into the beaker. Then put Plant A (the leaf exposed to air) into the boiling water for 3-5 minutes. After time is up, using tongs, place Plant A directly into the alcohol solution for another 3-5 minutes. When time is up, take out Plant A and place it into a clean petri dish. Once the plant is properly placed, cover the leaf completely
There are many procedures during this lab and many materials needed for an accurate analysis of data. First, fill a 100 mL graduated cylinder with 50 mL of water. Add 25 germinating peas and determine the amount of water that is displaced. Record this volume of the 25 germinating peas, then remove the peas and put those peas on a paper towel. They will be used for the first respirometer. Next, refill the graduated cylinder with 50 mL of water and add 25 non-germinating peas to it. Add glass beads to the graduated cylinder until the volume is the same to that of germinating peas. Remove the beads and peas and put on a paper towel. They will be used in respirometer 2. Now, the graduated cylinder was filled once again, determine how many glass beads will be require to reach the same volume of the germinating peas. Remove the beads and they will be used in respirometer 3. Then repeat the procedures used above to prepare a second set of germinating peas, dry peas and beads, and beads to be used in respirometers 4,5,and 6, the only difference is the temperature of the water.
In conclusion, the hypothesis is supported by the experiment. Only 2/10 disks floated to the top of the 0.1% NaHCO3 solution, while all 10 of the disks in the 0.2% NaHCO3 solution floated to the top. A potential follow-up experiment could be to test the affects of increased concentrations of carbonation on PS (Bagley et al., 2015). There was the possibility of human error and bias having impact on the experiment. When using syringes, the plunger may have been pulled too harshly and damaged some of the disks. This could have led to disks not floating to the top in the experiment. Another form of error could have been the use of disks that were cut from the veins of the leaf, which has less chloroplasts, meaning less process of photosynthesis happening, and result in the disks not floating to the
Vial number one had trouble staying down but my group held it under until finally they were able to get it to stay underneath the water. The rubber band could now be removed from the tray. The respirometers were in the water for a timed three minutes to allow them to equilibrate. After the three minutes was up the initial level of oxygen that entered the pipet was recorded in our lab books. After this data was found and recorded we were finally able to begin the actual experiment testing.
Abstract: The purpose of this lab is to separate and identify pigments and other molecules within plant cells by a process called chromatography. We will also be measuring the rate of photosynthesis in isolated chloroplasts. Beta carotene, the most abundant carotene in plants, is carried along near the solvent front because it is very soluble in the solvent being used and because it forms no hydrogen bonds with cellulose. Xanthophyll is found further from the solvent font because it is less soluble in the solvent and has been slowed down by hydrogen bonding to the cellulose. Chlorophylls contain oxygen and nitrogen and are bound more tightly to the paper than the other pigments.
At the end of each minute, record the number of floating disks. Then swirl the disks to dislodge any that stuck against the side of the beakers. Continue until all of the disks are floating. Create a graph of floating chads vs. time and analyze whether the green or reddish-purple leaves photosynthesized at a faster rate. Results
In the beginning of this experiment, our TA added water, salt, and 75/25 hexane/acetone to spinach leaves to a blender and blended the mixture to assume equal amounts for each group and to avoid erros if each student had to do the blending. The addition of the water to the mixture allowed the it to separate into a distinct organic layer after being run in a centrifuge, which was available to be collected at the top of the centrifuge. Salt reduces solubility, which will force the organic parts of the mixture (the desired pigments for example) to separate into the organic layer at the top. Lastly, 75/25 hexane/acetone is added because this is a moderately polar solvent and will useful for both the non-polar and polar pigments present within the spinach leaves. A mixed solution of hexanes and acetone must be used because acetone is very polar, while hexane in very non-polar, and the spinach leaves contain both non-polar and polar pigments in them that are important in the extraction and for further analysis. The mixture was placed in the centrifuge so the solids in the mixture (mostly cellulose) could be separated from the liquids into separate distinct layers for further extraction and testing. In the tube, the organic substances separated into the top layer, whereas the water layer remains at the bottom of the tube below the solid layer made up of mainly cellulose.
Photosynthesis is essential to all living organism such as animals and plants. Photosynthesis is a process used by plants and other autotrophs to capture light energy and use it to power chemical reaction that converts carbon dioxide and water into oxygen, carbohydrates and water. (Textbook: Principles of Biology). The reactants and the products of photosynthesis are:
The purpose of this lab is to observe the effect of white, green, and dark light on a photosynthetic plant using a volumeter and followed by the calculation of the net oxygen production using different wavelengths color of white and green light, and also the calculation of oxygen consumption under a dark environment, and finally the calculation of the gross oxygen production.
However one beaker received 100 mL of Deionized water with a molarity of 0.0. Afterwards a cork borer was pushed through the potato and was twisted back and forth. Once the borer was filled it was removed from the potato. Pushing the potato cylinder out of the borer, this this step was repeated six more times in order to get seven undamaged potato cylinders. Using a sharp razor blade, the potato cylinders were both cut to a uniform length of about 5cm, and were removed of their potato skins. The potato pieces were also cut in half to give the cells a greater surface area in which it was easier to absorb the solution. After the cylinders were weighed on a balance and the data was recorded in Table 4. Using the razor blade each potato was cut lengthwise into two long halves. Then the potato pieces were transferred to the water beaker and the time they were submerged was recorded. This step was repeated for all potato cylinders in which the pieces were placed in solutions 0.1 to 0.6 M. The potatoes were incubated for ninety minutes. At the end of the incubation period the time was recorded. Then the potato piece was removed form the first sample. Next potato pieces were weighed the and the final weight was recorded in Table 4. This procedure was repeated until all samples had been weighed and recorded in the chronological order they were initially placed in the test solution. Afterwards the table was completed by recording the
The process of photosynthesis, by which light energy is used to convert inorganic compounds into organic substances with the release of oxygen, may be the most important biological event sustaining life (Keir et al. 2017). In the light-dependent reactions, the chloroplasts of a plant use the pigment chlorophyll to convert light energy into chemical energy. This energy is used to split water and produce oxygen (Eller et al. 2015). The energy is later used in the light independent reactions, where carbon dioxide (CO2) undergoes carbon fixation with the aid of enzyme rubisco, because it catalyses both carboxylation and oxygenation reactions and most of responses of photosynthesis to light, CO2, and temperature (John Evans 2013).
For lab 12, it is hypothesized that chlorophylls a and b are present in a plant leaf and contribute to the starch production in photosynthesis. Also, products of photosynthesis will be present in leaf tissue exposed to red and blue light wavelengths for several days, but a decreased presence in leaf tissue exposed to green and black light wavelengths. In lab 13, it is expected that since chlorophylls a and b are more polar and smaller molecules than the anthyocyanins and carotenoids, they will travel higher up the chromatography paper than the other pigments.
The next step was to place the strip of chromatography paper on a paper towel. Then dip a capillary tube into the plant pigment extract (spinach pigment extract) provided by the teacher. The tube will fill on its own. We applied the extract to the pencil line on the paper, blew the strip dry, and repeated it three to four times until the line on the paper is a dark
Photosynthesis is a vital process that autotrophs use to transfer light energy into chemical energy. Photosynthesis ultimately produces O2 and glucose. It, like many other biological processes, can be affected by environmental variables. The variable that we altered in the following experiment are intensity, light wavelengths, and pigment types. In order to do this, we conducted three experiments. In the first experiment, we examined the effect of light intensity by placing vials with chloroplasts with DPIP at different light distances in which the results varied. Initially, 30cm away was the most effective for photosynthesis. Then 24cm appeared to be the most effective. Followed by 49cm at minutes 25 and 30. In the second experiment, we
Then, each group of students received the necessary materials to complete the experiment. When the students received the cups, they labeled cups to distinguish between the salt solution, distilled water, and control group. After weighing the cups and finding the mass of the cucumbers, the students poured 50 ml of water in one cup, 50 ml of salt solution in the other, and left the control cup empty. Then, the students placed the cucumbers into the cups and waited 30 minutes for the results. After the 30 minutes, the students removed the cucumbers from each solution and dried the cucumbers with paper towels. The students then weighed the cucumbers again and recorded their results. Lastly, the students found the difference from the original mass of the cucumbers and recorded their results.