THE EFFECTS OF AMMONIA AND VINEGAR ON RADISH PLANTS 1
The Effects of Ammonia and Vinegar on Radish Plants
THE EFFECTS OF AMMONIA AND VINEGAR ON RADISH PLANTS 2
Abstract
INTRODUCTION OF GROUP Plants are one of the most complex organisms; how they grow is very complex and it is important to see how they grow to even how they die. We first had to propose a question and test it to see if it was profound enough to test. Our group decided to see how different chemical substances affect radish plants, and which substance will kill the plant fastest. We planted 8 germinated radish seeds, then put ammonia in 2 of the plants, vinegar in 2 other plants, put both vinegar and ammonia in 2 other plants, and had the
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Vinegar is also used in diet control because several doses can provide feeling of fullness and satisfaction. It is also an effective screening tool for cervical cancer because vinegar changes the color of the tissue that is infected to a color of white so it can be easily noticed. Vinegar is also a cleaning agent because of its acidic property it can dissolve mineral deposits from glass. Vinegar is a very useful chemical substance but at the same time a very acidic and corrosive compound (Harris, 2011).
THE EFFECTS OF AMMONIA AND VINEGAR ON RADISH PLANTS 4
Methods
The group planted a total of 8 separate pots of seeds. Two pots consisted of only seeds and those were the control group of this experiment. The other plants also consisted of radish seeds but had chemicals ammonia, vinegar, or a combination of both applied once weekly with 30ml of water being applied daily (except on the weekends). As a result, there were a total of 8 pots. Two of each variable and two of the controls. Right after all the seeds were germinated in petri-dishes they were put into pots, covered with soil, and labeled to prevent confusion.
2 pots were labeled as: CONTROL - One of which was labeled control 1 and the other control 2
2 pots were labeled as: VINEGAR -One of which was labeled vinegar 1 and the other vinegar 2
2 pots were labeled as: AMMONIA -One of which was labeled ammonia 1 and the
The experiment was begun by obtaining four 8 oz. Styrofoam cups and punching a hole through the bottom of them. This hole was for water entry or excess water drainage. Moistened soil was packed to the 1/2 full line in the cup along with 3 fertilizer pellets The cups were labeled the following: Rosette-H20, Rosette-GA, Wild-Type-H2O, and Wild-type- GA.(Handout 1) A small wooden applicator stick was obtained a moistened at the tip with water from the petri dish labeled ‘water.’ This was to be able to attract the seed to the applicator in order to place the seed from its original container into
The results obtained are non-conclusive. More research is necessary in order to fully understand the effects of Nitrogen in the development of Fast Plants seeds and the soil. It is recommended that original is repeated. However, only one fertilizer should be added per quad, rather than mixing the fertilizer used for the control with the fertilizer being studied. For future studies it is also recommended to maintain a record of the pH of the soils before, during, and after the experiment in order to understand the impact of fertilizers on the
The low-density radish-collard mix pots contained four seeds of radishes and four seeds of collards. The high-density radish-collard pots contained 32 seeds of each species. While our group replicated this 3x2 design four times to total 24 posts, we incorporated the whole class data. Therefore, there were 16 replicates for each treatment. For each pot, we filled soil up until about one inch from the top. We placed the seeds in the pot and piled on around 2 or 3 cm of soil on top. In 3 species levels, seeds were spaced as evenly as possible. In the mixed species pot, the two species were alternated so that each one had the same access to space and nutrients at the other. For each pot, we wrote down our section number, group name, and the contents of the pot. Our group worked at the first bench in the greenhouse and also contained our pots that were spread out evenly in four rows. Our pots stayed in the greenhouse for about five weeks, captured as much sunlight as they could, and got their water source from sprinklers that automatically came on twice a
In this experiment we are testing the effect of fertilizer on the speed of plant growth. We prepared a 4 quad cell, 1 control group and 3 experimental groups. So, we had one with no fertilizer, one with three seeds of fertilizer, one with six seeds of fertilizer, and lastly, one with nine seeds of fertilizer. The plants that we grew were called Wisconsin Fast Plants, members of the crucifer family. These plants are small and easy to grow, but for optimal growth they require continuous fertilizer, water, fluorescent light, and temperature between 18 degrees Celsius and 26 degrees Celsius 24 hours a day. Fertilizers are substances that are put into soils to increase the growth of the plant. There are two different types of fertilizers, synthetic
all treatments contain the same type of soil, are planted in the same size of pan, are exposed to the same amount of sunlight, and are maintained at the same temperature throughout the course of the experiment. ON THE TEST there will be a number of related questions about this section not just the question shown below.
The purpose of this experiment is to observe the effects of Sodium Chloride (NaCl) on the germination rate of Wisconsin Fast Plants.
51) A botanist wanted to see if a new strain of corn could germinate in soil that was too salty for regular corn. She conducted a study on the germination success of seeds from the new strain that were exposed to various levels of salty soil, from zero to normal (100mg/L) to high (200 mg/L) to very high (400 mg/L) to normally lethal (800 mg/L)
In the dishes, I dropped the appropriate treatment into the center, where the marks were made. Next, I closed the petri dishes, taped them up, and let them sit at room temperature for a week. Then I opened them up to take two measurements. The first measurement was the number of seeds germinated. The second measurement was to measure the seedling lengths.
The third step that was taken was germinating the seeds. Two sets of paper towels were used to germinate the
For my seed experiment I had decided to see what the effect of sprinkling salt on a radish seed would be. So for my control group I had set six (6) cherry radish seeds in between a damp paper towel and then closed it within a Ziploc bag. For my experimental I had set it up the exact same way as the control group but I would sprinkle salt on top of seeds before I zipped up the baggie. I sprinkled the salt on the experimental seeds and dampened the paper towel once every day. Each bag was stored in the light and at room temperature (~70° F.)
The experiment that the class worked on was about peroxidase. Peroxidase is part of the enzyme group that presents most living organisms (Ahmed, 2013). Peroxidase interferes with the removal of hydrogen peroxide (Ahmed, 2013). Hydrogen peroxide is a toxic product that have normal metabolism before it causes any cell damages (Ahmed, 2013). Peroxidase has two substrate and both of them must present a reaction (Ahmed, 2013). One of the two substrate is H2O2 and other one just depends on the organism or the cell type (Ahmed, 2013). The substrate that the class uses is turnip extract. In the class there were five experiments to do but the class were assigned into groups and each group were going to do two experiment. The names of the experiments are: Baseline, Temperature, and pH.
Apple cider vinegar is one of the healthiest cleaning products available. It sanitizes and disinfects surfaces just as well as products containing harsh chemicals. It can clean carpets, clothing, floors, and dishes so well that they sparkle. Some people use it to wash their fruit and vegetables after purchasing them from the market. It also reduces inflammation and calms troubled stomachs. If taken on an stomach before a meal,
Therefore, I was correct in my hypothesis that dark will have an effect on the germination of radish seeds. Also, I was very close in predicting that the seeds grown in the light will germinate twice as much as the seeds grown in the dark; the control seeds grew a little less than double the size of the experimental seeds. Ultimately, my experiment proved that light is a very important factor in the growth of any plant. However, I’ve learned that seeds grown in the dark will germinate, though slowly, as
In the experiment we used Turnip, Hydrogen Peroxide, Distilled Water, and Guaiacol as my substances. On the first activity, Effect of Enzyme concentration of Reaction Rate for low enzyme concentration, we tested three concentrations of the turnip extract, and hydrogen peroxide. For the Turnip Extract I used 0.5 ml, 1.0 ml, and 2.0 ml. For hydrogen peroxide we used 0.1 ml, 0.2 ml, and 0.4 ml. We used a control to see the standard, and used a control for each enzyme concentration used. The control contains turnip extract and the color reagent, Guaiacol. We prepared my substrate tubes separately from the enzyme tubes. My substrate tube
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.