For this experiment, we used a solid piece of styrofoam tray that served as the confines for our experiment. We then gathered three different types of environments, sand, soil, and a leafy mixture, and separated each equally into each corner of the styrofoam board. We used five pill bugs in the first part of the experiment. This created four different settings on the board that the pill bugs could choose from. For the group part of the experiment, we used one stopwatch to keep a total time that the pill bugs were placed in the styrofoam board, a total of five minutes. For this part of the experiment we did not keep track of the total time that the bugs spent in each environment, but instead recorded the environment that the most bugs were
Acidity of an ecosystem, measured in pH, is a crucial factor to the survival of a species in an ecosystem. Altering it can have result in dramatically negative effects, in spite of the fact that pH of an ecosystem has been dramatically changed over a relatively short period of time due to various human activities. For example, acid rain is a major environmental problem that is caused by human-made pollution. When fossil fuels are burnt to get energy, pollutants like sulfur dioxide and nitrogen oxides get mixed into the rainwater and eventually are evaporated into the atmosphere. These gases enter the atmosphere, and mix with water in the water cycle to form an acidic mixture of water and gases. This water falls in the form of acid rain, which
We conducted a controlled experiment to determine which variable, Music or no music, would have the greater averaging effect on the pillbugs.
Wet and Dry Environments To find whether Pill bugs gravitate toward a wet or a dry experiment, two coffee filters were cut to the size of the petri dish and placed inside, however one was dampened before being placed on the bottom. Dirt was then added on top to promote a more realistic environment and five Pill bugs were placed in each side before starting to prevent bias on an environment. A log was taken every thirty (30) seconds for ten (10) minutes on how many bugs were in each chamber and a graph was then made to show the changes of the bugs' positions over time. Again, if a Pill bug was in the transgression tunnel he was determined to be in a dish by the direction he was moving or the way it's head was facing.
The dependent variable is pulsation rates of L. variegatus before and after they were in the treatments. The standardized variable of this experiment would be the temperature of the surroundings of the L. variegatus, the three pulsation rates taken for each worm before and after the treatments, and also the amount of time each worm was kept in their respective treatments. The level of treatment for this experiment would be ten because of the six different concentration treatments of caffeine and nicotine along with the four household drugs. The sample size of the experiment differed from some treatments to other. For the three different concentrations of caffeine and nicotine, the sample size was 18 black worms each. The sample size of the control treatment of week 1 was 6 black worms. 12 black worms were used for the control of week 2, decaffeinated coffee and instant coffee. 11 black worms were used for the tea treatment and 15 were used for the tobacco treatment. There were three replications of the pulsation rate readings per worm before and after the treatment. With all this information we were able to get the results we got.
As an experiment I would place multiple kinds of cereal in front of a single mealworm, and record their reactions to each certain type of
The hypothesis that was tested was pill bugs are use to the cooler temperature of the room and natural soil would travel a greater distance once they were in a hotter environment. The hypothesis is rejected on the basis that the p-value of .760 is greater than .05. Furthermore, figure 3 supports this rejection, since the averages are very close to each other and their error bars completely overlap. This rejection means that once the pill bugs where in the hotter environment there was not difference in their behavior compared to the cooler room temperature environment; they did not travel longer distances. However looking at bugs D, F G and H in figure 2, there is a difference in distance traveled that appears to be greater than
2. Place 10 randomly selected sowbugs in each of the 3 empty tin bowls for 3 minutes to allow them to acclimate to the environment.
The Pill Bug Lab created many various trends or patterns in the data. The data in figure 2 show that towards the beginning of the experiment, the pill bugs were very active in both the wet and dry environments. This is because the Pill Bugs were suddenly placed in an environment they had not been in before, so there first reaction was to find a place of comfort to settle in. Over time, which figure 1 shows, many pill bugs switched from one location to another and continued to move back and forth. As the experiment was coming to an end, the data shows that the pill bugs slowly started to settle into their final destination.
This experiment was performed to observe the taxis and kinesis of certain organisms. This is important because the organism’s survival and ability to reproduce depends on how they orient to stimuli using senses. We investigated the behavior of pill bugs to determine if they’ll move towards or away from the vinegar through smell. If I place pill bugs in a behavior tray with different chambers, then they’ll move away from the chambers that contains vinegar. A behavior tray with 5 chambers is used and 2 were control while the other 2 has cotton balls with a few drops of vinegar on it. 5 pill bugs are positioned in the center of the chambers and is covered with a transparent cover to observe the organisms for 10 minutes. Results had shown the class
One sowbug was then placed in the 3cm gap of the container and 30 seconds was started on the stopwatch. When time was completed we observed which side, grass or sand, the sowbug had preferred. Then, the sowbug was removed and a new one was placed in the container. The same steps were taken for each of the 20 bugs.
Next the beetle was weighed and it’s weight was recorded. The dental floss was then tied around the second and third legs, and taped to the petri dish. A strip of cloth was also needed to provide traction for the beetle. Then, the petri dish was removed from the beetle and the weight of the petri dish was recorded. The experiment was then ready to be performed. Paperclips were added to the dish every 5-10 seconds until the beetle could pull it no more. Then, the petri dish was removed from the beetle and the weight of was recorded. This experiment’s dependent variable was the amount of mass the beetle can pull, and the independent variable was the mass of the beetle. There was no control group in this experiment. These were the materials and methods used to conduct this
The purpose of our experiment is to test animal behavior and reactions to a change in environment. Our guiding question is, “Why do living organisms respond to environmental factors?” This is basically a question that is asking why living things will react a certain way to environmental changes. The task to answer this question is to experiment with changing environmental factors with pill bugs.
We put equal amounts of sand or dirt in each chamber, as well as 6 mL of water mixed in on either side. Afterwards, we placed 12 pill bugs in the bridge between the dishes. This allows the pill bugs a clear choice between the two materials. We recorded the number of pill bugs on the dirt dish, sand dish, and bridge each minute for seven minutes in a chart. We did this to indicate any movement the pill bugs might have performed during the experiment.
The containers were plastic and 18 by 15 by 6 centimeters long. Prior to the experiment being performed, the crickets had spent a week in these residencies. Along with the crickets in the plastic containers, there was wet pieces of paper towel and a slice of carrot.
METHODS: In this experiment, the instructor provided us with 30 ebony individuals and 20 wild type individuals. In order to get an exact amount of each type, we anesthetized the flies and counted them off by gently using a fine point paint brush. Then all 50 Drosophila were put into a population cage which had a lid that had six holes for the centrifuge tubes. Two food tubes and four clean, empty tubes were added on the first day. Each food tube consisted of half a cup full of food mixed with 6-7 milliliters of water. This was the fly medium. The food should turn blue once the water is added. Each tube was labeled with a number and with the date. Every two to three days we added one more food tube until all 6 tubes contained the fly medium. After all 6 tubes were filled, the following days after we exchanged the first food tube with a new food tube. At the end of the experiment, we fed the flies with a total of 8 food tubes. Then the flies were anesthetized, again. At the end of this four week lab, the number of living ebony and wild