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Phuong Lam-Bio 206L Research paper

Course: ECO 304K 304K, Spring 2012
School: University of Texas
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the Does limited food resources affect the level of aggression in male crickets? Phuong Lam BIO 206, Spring, 2011 Unique # 48840, Mary-Kay Johnson April 26th, 2011 Does the limited food resources affect the level of aggression in male crickets? Abstract: Limited of resources such as shelter, food, air, etc. could lead to many aggressive behavior in animals, including crickets. Crickets have been used as great...

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the Does limited food resources affect the level of aggression in male crickets? Phuong Lam BIO 206, Spring, 2011 Unique # 48840, Mary-Kay Johnson April 26th, 2011 Does the limited food resources affect the level of aggression in male crickets? Abstract: Limited of resources such as shelter, food, air, etc. could lead to many aggressive behavior in animals, including crickets. Crickets have been used as great model organisms for the aggressive behaviors. In this experiment, we have observed roughly about 80 crickets on their aggressive behaviors based on food (variable group) and no food (control group). Crickets were starved for a week before the experiment to see if they were willing to compete for only one food pellet. Hunger can drives the crickets to fight for their survival. The observations were recorded based on 6 behaviors such as latency, antenna fencing, mandible spreading, mandible bite, wing movement, and chirping during the contest between two male crickets. We hypothesized that limited resource lead to more aggressive behavior in order to earn the food. Through out the experiment, we observed that the one who did not get the control of food first tend to start latency to fight for the food. However, the one with the control of food for the longest time seemed to be more aggressive in order to protect his resource. They are what we call the winner. Although we saw more aggressive behaviors on the graphs if limited resource (food pellet) was involved between the two male crickets, the T-test of the data has shown that there is not enough evidence (statistically insignificant) in the experiment to prove that level of aggressive behaviors in crickets due to limited resources. Introduction: Crickets aggressive behaviors have been observed for many years (Alexander, 1961), (Rillich, et al., 2007). Crickets are very convenient models for observing aggressive behavior because not only do many species compete for limited territory, food, and shelter (Hsu, 2006), but they can also display highly aggressive agonistic interactions. Several noteworthy communication methods are displayed during fighting including antennal fencing, mounting, spreading of the mandibles, and mandibles biting (Alexander, 1961), (Briffa, 2008), (Brown, 2006), (Hofmann, Stevenson, 2001), (Stevenson, et al., 1999), (Tachon, et al., 1999), which carry both motivational signals as well as signifying their strength. Other displays observed during combat include body jerking and a rivalry song. Different species differ in the sequence of agonistic behavior, some displaying these behaviors only for competition for survival resources or mating, and others escalating in an encounter with other males or while being isolated for a period of time (lab manuel). Interestingly, frequent competition between male crickets is an essential factor that has led to these types of agonistic behaviors over time (Hack, 1997). Since the most important resources to crickets are territories, food, and mating partners and when the number of resources in the population decreases, the value of their territory and willingness to defend it is more likely to increase (Hofmann and Schildberger, 2001). We carried out an experiment to see the level of aggression if there was limited food resource. In our experiment, we hypothesized that in the cricket species, Acheta domesticus, aggression level increases if they must compete for limited resources. Methods and Materials: In our cricket experiment, we had total of 84 male crickets. These crickets were isolated and starved for about one week before the experiment. The crickets with colorcoded on the top of their heads to help us distinguish different crickets when we recorded data. The observation sand-covered arena (which was a big clear box with compartment dividers) was provided as a location for the contests between these crickets. We had a control group, which was no food, and a variable group with food pellet. Half of the experiment, which totaled of 42 crickets, was for contests without food and the other half was for fights with limited food. We prepared an Excel with different sections for observed behaviors for data recording. These observed behaviors included latency, antenna fencing, mounting, mandible spreading, mandible bite, chirping, and wing movement. We did not weight and measured the length of the crickets before the crickets encounter to ensure that no external factors affect the experiment results. Due to some unexpected circumstances, few crickets died during the experiment. Therefore, we ended up with less crickets for the experiment then we were given. We got data from 20 sets with-food contests and 19 with-no-food contests. For limited food resource contests, we placed two male crickets in separate compartments and allowed them to acclimatize the surrounding for about 1 minute. After a minute has passed, we removed the divider and immediately dropped in the food pellet. The observation for the contest between each set of crickets was about 5 minutes long. Then we observed the encounter between those two crickets and recorded down the behaviors that listed above. After all the with-food-contest was completed, we then did the same steps for no-food tests except with no food pellet. The crickets were removed from the arena and we measured the weight of each on the top loading balance and the length with standard metric ruler. Results: Before I analyzed the results of my experiment, I carried out two tests: Kolmogorov-Smirnov and T-test. First, I used Kolmogorov-Smirnov Comparison of two data sets to test the normality of the data. Based on the result of the K-S test, it shows that our data is not normally distributed (K-S test p-value for food is 0.00 and p-value for nofood is 0.04). However, to increase power of our analyses, I chose parametric tests. I used an unpaired T-test to examine cricket behaviours with respect to food vs. no food. The calculation was determined to compare the results between the two data, food vs. no food total aggressive acts. The variable group with-food has the total aggressive acts with mean of 10.5 and standard deviation is 6.73. For no-food total aggressive acts, mean = 8.13 and stdev = 6.51. Based on the T-test result, the variable group with food is not statistically significant (T-test, t-value= 1.66, 76 p-value= df, 0.122) compared to control group of no food. Even though, the T-test shows that with-food total aggressive acts is not significant, the following graph somewhat shows that there is some difference between groups of food vs. no food. The bar graph shows the frequency of aggressive acts and the lines above the bars represent the error or standard deviation away from the mean. Figure 2 is graph on specific aggressive acts, antenna fencing. This also shows that with limited resource, they tend to show more aggressive behavior, specifically antenna fencing. Figure 1: shows the mean of aggressive acts (y-axis) with food and no food (x-axis) Figure 2: the mean of antenna fencing (y-axis) with food and no food (x-axis) Discussion: Crickets behaviors for different reasons such as food, shelter, mates, etc. have been studied and observed by many scientists and researchers. In this experiment, we performed an experiment that similar to many that have been done to show if the levels of aggression in crickets increase if they have to compete for limited resources. Based on the result of T-test (students t-test, t-value= 0.122), 0.122 is greater than 0.05 (level of significant). Therefore, the data is not statistically significant and we fail to reject the null hypothesis that the level of aggression is not due to the limited resources. This result is the opposite of what we expected. However, there could have been possible errors that affect the results during the experiment. First of all, two crickets unexpected died and some group provided missing data; therefore, the numbers of sample size were actually smaller than what was planned. Secondly, there could have been possible errors while observing the behaviors of crickets such as miss counted the different behaviors and misheard the chirping of the crickets due to the loudness in the room. Also, the behaviors of crickets were observed by different students, thus, each of us could have interpreted the behaviors slightly different. Throughout the experiment, we have observed that cricket, whose in possessed of food tend to be more aggressive to protect his asset against the other cricket, who wanted to get control of the food pellet (Nosil, 2002). Another point that showed the trend for the winner, who had the control of the food longest, was if he had the acquired the food pellet first (Nosil, 2002). Contemporary sociobiological and behavioural concepts envisage the complex escalating fighting strategies characteristic of intraspecific aggression as having evolved in order to enable an individual to secure limited resources at minimal cost (Rillich, et al. 2007). Antennal contact between the crickets usually triggers the aggressive behavior (Kaushik, et al., 2009). The crickets recognize the opponents by chemicals they secrete (Ghosal, et al. 2010). We observed the escalating sequence of aggressive behaviors when the crickets encounter each other. These escalating sequence included from antenna fencing, body rocking, chirping, flaring of the mandibles, and wresting/mounting (Tachon, et al., 1999), (Leslie and Walker, 2007). We noticed that the losers in the contests tend to try to escape avoiding contact with the dominant male. (Ghosal, et al. 2010). The owners probability of winning the contest will be grater when the value of the resource is greaterthe costs of contest would rise for both individuals as the value of the resource increased. (Buena, Walker, 2008) References: Alexander, R. D. (1961). Aggressiveness, territoriality, and sexual behavior in field crickets (Orthoptera: Gryllidae). Behaviour, 17(2/3), 130-223. Arnott, G., & Elwood, R. W. (2009). Assessment of fighting ability in animal contests. Animal Behaviour, 77, 991-1004. Briffa, M. (2008). Decisions during fights in the house cricket, Acheta domesticus: mutual or self assessment of energy, weapons and size. Animal Behaviour, 75(3), 1053-1062. Brown, W. D., Smith, A. T., Moskalik, B., & Gabriel, J. (2006). Aggressive contests in house crickets: size, motivation and the information content of aggressive songs. Animal Behaviour, 72(1), 225-233. Buena, L. J., & Walker, S. E. (2008). Information asymmetry and aggressive behaviour in male house crickets, Acheta domesticus. Animal Behaviour, 75(1), 199-204. Ghosal, K., Naples, S. P., Rabe, A. R., & Kilian, K. A. (2010). Agonistic behavior and electrical stimulation of the antennae induces Fos-like protein expression in the male cricket brain. Archives of Insect Biochemistry and Physiology, 74(1), 38-51. Ghosal, K., Gupta, M., & Killian, K. A. (2009). Agonistic behavior enchances adult neurogenesis in male Acheta domesticus crickets. The Journal of Experimental Biology, 212, 2045-2056 Hack, M. A. (1997). Assessment strategies in the contests of male crickets, Acheta domesticus (L.). Animal Behaviour, 53, 733-747. Hack, M. A. (1997). The energetic costs of fighting in the house cricket, Acheta domesticus L. Behavioral Ecology, 8(1), 28-36. Hofmann, H., Allen, B., & Draper, M. (2011). Aggressive Behavior of Crickets. In Laboratory Manual (p. 313). Austin, TX: School of Biological Sciences The University of Texas. Hofmann, H. A., & Schildberger, K. (2001). Assessment of strength and willingness to fight during aggressive encounters in crickets. Animal Behaviour, 62, 337-348. Hofmann, H. A., & Stevenson, P. A. (2000). Flight restores fight in crickets. Nature, 43, 613. Hsu, Y., Earley, R. L., & Wolf, L. L. (2006). Modulation of aggressive behaviour by fighting experience: mechanisms and contest outcomes. Biology Review, 81, 33-74. Nosil, P. (2002). Food fights in house crickets, Acheta domesticus, and the effects of body size and hunger level. Candian Journal of Zoology, 80, 409-417. Rillich, J., Schildberger, K., & Stevenson, P. A. (2007). Assessment strategy of fighting crickets revealed by manipulating information exchange. Animal Behaviour, 74, 823-836. Stevenson, P. A., Dyakonova, V., Rillich, J., & Schildberger, K. (2005). Octopamine and Experience-Dependent Modulation of Aggression in Crickets. The Journal of Neuroscience, 25(6), 1431-1441. Tachon, G., Murray, A.-M., Gray, D. A., & Cade, W. H. (1999). Agonistic displays and the benefits of fighting in the Field cricket, Gryllus bimaculatus. Journal of Insect Behavior, 12(4), 533-543.
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