Sordaria Lab

Effects of chase aftering Over in Sordaria fimicola Abstract Sexual sound reflection in organisms is a cause for genetic disagreement. This loafer be moldn with the process of meiosis in Sordaria fimicola because of the effects of fording oer and main(a) assortment that get along in meiosis I. Before performing this experiment we hypothesized that we would be able to see that ball uping everywhere did indeed occur in the S. fimicola. We tested our hypothesis by growing our own culture and observing it under(a) a microscope. By counting and recording the types of asci we were able to find that our hypothesis had been correct.This has now led us to know that sexual reproduction causes an increase in genetic variation in organisms such as, Sordaria fimicola. Introduction Organisms reproduce in 2 ways asexually and sexually. Sexual reproduction can be specify as the reproduction involving the union of gametes or when genetic material from cardinal parents combine to form o ffspring (Cyr). Offspring produced from sexual reproduction look at a unique genetic make-up, which can any be beneficial or destructive to them (Saleem). Close to all known organisms use this kind of reproduction during some moment in their lifetime.If this is true, however, why is not every species seemingly genetically identical? To answer this, one must observe the chromosome behavior during the sexual reproduction life cycle also known as meiosis. Meiosis is the process of cell division in which gametes are produced. It results in intravenous feeding haploid (IN) cells from two diploid (2N) cells (Cyr). In meiosis I, crossing over and independent assortment of the chromosomes occur. These two processes increase the genetic variation within the cell either benefiting or hurting the cells ability to adapt (natural selection). later on these two events have occurred, the chromosomes will therefore proceed through all four stages and produce two daughter cells (Cyr). In meiosi s II, the two daughter cells each again proceed through all four stages and produce a final four distinctly incompatible daughter cells (Cyr). Sordaria fimicola allows us to see observe the process of meiosis. This is because its life cycle is rapid and allows scientists to observe many generations in a pithy amount of time (Meiosis). Also, the size of S. fimicola makes it easily viewable under a microscope.Experiments with Evolution canyon have shown exactly how S. fimicola is a representative organism for crossing over. Evolution Canyon represents the whole idea of different locations in Israel containing two mountain slopes exposed to vastly different climatic conditions that converge with a vale between them (Meiosis). In each of these cases, one slope has been exposed to harsh conditions while the other has been exposed to temperate conditions (Saleem). Because each slope undergoes different conditions, we can observe how genetic variation is affects the S. imicola that live on each slope. Scientists gathered samples of the organism living on both slopes and analyzed the differences in crossing over and the differences in crossing over frequencies. The purpose of our lab is to observe the different cross over frequencies. We want to compare and contrast the crossover frequencies in different coloration strains of S. fimicola. We hypothesize that in this experiment we will observe crossing over occur in the Sordaria fimicola after two weeks of growth in the agar plates.To test our hypothesis, we will grow our own asci spores in an agar plate and observe the organism under the microscope while recording the different ascus types which can either be type A (44), type B (242), or type c (2222). Materials and Methods From the Meiosis and factortic Diversity in Sordaria handout, we found the materials and procedure for this experiment. Equipment that we needed to perform the first part of this experiment were two agar plates, a marking pen, a scalpel, and two different color strands of S. imicola. The first step in this lab was to mark two separate agar plates with the marking pen in such a way as to create four separate quadrants on each agar plate. Second, each plate needed to be labeled, identifying it as either the plate with tan fungus kingdom or senile fungi. Next, using the scalpel, a small piece of the samples of S. fimicola had to be sliced and placed in the corresponding spots in the agar plates. The plates then were taped and allowed two weeks to grow. After two weeks, the samples had flourished.We first scooped up small portions of each of our samples and put them on a slide with a drop of water, creating squashes, to be viewed under the microscope. When viewing under the microscope, each of the four group members counted and recorded their own twenty asci. While recording, each member categorized whether the asci they found had equal type A, type B, or type C recombination type. Last, when each member had attained thei r individual cultivation, we combined our data to create a total data for our entire group. Then we proceeded to combine our data to find a section and a course total.Results Four separate sectors analyzed the data of this experiment, the individual, the group, the class, and the section. The results were as follows Cross Over Frequency Percent of Cross Over = (Number of Recombinant Asci / come in Number of Asci ) X atomic number 6% Individual Cross Over Frequency = 12/20 X nose candy% = 60% (gray) Combined chemical group Cross Over Frequency = 24/40 X 100% = 60% (gray) Combined grouping Cross Over Frequency = 28/40 X 100% = 70% (tan) Combined Section Cross Over Frequency = 128/220 X 100% = 58% (gray) Combined Section Cross Over Frequency = 163/260 X 100% = 62. % (tan) Combined Course Cross Over Frequency = 4054/7066 X 100% = 57% (gray) Combined Course Cross Over Frequency = 8277/13946 X 100% = 59% (tan) After examining the cross over frequencies of the four sectors of data, we can see that for both the gray and tan spores an average of 60% were recombinant. This means that on average, 60% of the time S. fimicola will cross over resulting in spores of type B (242) or type C (2222) Map surpasss Map Distance from Cross Over = Percent Cross Over / 2 Individual Map Distance = 60%/2 = 30 mu (gray) Combined Group Map Distance = 60%/2 = 30 mu (gray) Combined Group Map Distance = 70%/2 = 35 mu (tan)Combined Section Map Distance = 58%/2 = 29 mu (gray) Combined Section Map Distance = 62. 6%/2 = 31. 3 mu (tan) Combined Course Map Distance = 57%/2 = 28. 5 mu (gray) Combined Course Map Distance = 59%/2 = 29. 5 mu (tan) Again, the map distances for both the gray and tan spores averaged about 30 mu. This means that on average there were 30 units between the cross over and the centromere of the chromosome. The fact that all of the map distances are around the same number also helps to represent the accuracy in our results. Discussion After observation of the Sordaria fimicola, we were able to depict the different types of crossing over.This supports our hypothesis crossing over did occur in the S. fimicola. Because we were able to see that crossing over did occur and examine the three different cross over types, we can now say that sexual reproduction attributes to increases in genetic variation. We can see this by the 60% cross over frequency of the recombinant (type B and type C) spores in both the gray and tan strands. This example of the process of meiosis shows us that independent assortment and crossing over attributes to the variety of offspring that are produced in Sordaria fimicola.This life-size variety leads us to know natural selection plays a large role in the life cycle of fungus and especially S. fimicola. Our experiment showed baseline data under the same conditions as Evolution Canyon. While Evolution Canyon showed the effects of cross over frequency as the two spore strands adapted to their different environmental conditions, our experiment showed the cross over frequency of S. fimicola under public conditions. This baseline allowed for the comparison of the strand types that had become adapted to their different environmental conditions on Evolution Canyon. Errors that could have occurred during this experiment were the recounting of asci. There may have been replication of certain asci strands. The experiment, however, is liquid reliable due to the large number of spores counted. This large number of 7066 gray spores and 13946 tan spores allowed for a reliable average to still be found. Future experiments may find this information useful because it gives insight into the how often crossing over occurs and therefore at what rate genetic variation is happening. By knowing more about genetic variation rate, we can learn more about evolution and how that effects natural selection.Experimenters could use this information to compare the rate of genetic variation to the effects it has on natural selection. References Cyr, R. 2002. Heredity and the Life Cycle. In, Biology 110 Basic concepts and biodiverity course website. Department of Biology, The protactinium State University. http//www. bio. psu. edu/ Meiosis and Genetic Diversity in the Model Organism, Sordaria. Written by Hass, C. and Ward, A. 2010. Department of Biology, The Pennsylvania State University, University Park, PA. Saleem, Muhammad. 2001.Inherited Differences in Crossing Over and Gene Conversion Frequencies Between Wild Strains of Sordaria fimicola From Evolution Canyon. University of Haifa, Israel. Figures and Tables Table I. Individual Data Non-recombinant Recombinant Recombinant Total of Asci Total Recombinant Asci (B +C) of fictional character A Asci of Type B Asci of Type C Asci 8(gray) 7(gray) 5(gray) 20(gray) 12(gray) This represents the 20 asci counted individually. Of these twenty, twelve were recombinant meaning crossing over took place. The other were not recombinant and therefore crossing over did not occur.The crossover frequency was 60%. Table II. Combined Lab Group Data Non-recombinant Recombinant Recombinant Total of Asci Total of Recombinant Asci (B+C) of Type A Asci of Type B Asci of Type C Asci 16(gray) 15(gray) 9(gray) 40 (gray) 24(gray) 12(tan) 13(tan) 15(tan) 40 (tan) 28(tan) This represents the spores counted for our entire group of four people. Of the 40 gray spores counted, 24 were recombinant meaning crossing over took place while 16 were non-recombinant. The crossover frequency for the gray spores was 60%. Of the 40 tan spores counted, 28 were recombinant while 12 were non-recombinant.The crossover frequency was 70%. Table III. Combined Section Data Non-recombinant Recombinant Recombinant Total of Asci Total of Recombinant Asci (B+C) of Type A Asci of Type B Asci of Type C Asci colourize Spore 92 67 61 220 128 Tan Spore 95 72 91 260 163 This represents the spores counted by the entire class. Of the 220 gray spores counted, 128 were recombinant and crossing over took place while 92 were non-recombinant. The crossover frequency was 58%. Of the 260 tan spores counted, 163 were recombinant while 95 were non-recombinant.The cross over frequency was 62. 6%. Table IV. Combined Course Data Non-recombinant Recombinant Recombinant Total of Asci Total of Recombinant Asci (B+C) of Type A Asci of Type B Asci of Type C Asci Gray Spore 3012 2081 1973 7066 4054 Tan Spore 5669 4301 3976 13946 8277 This represents the spores counted by the entire section. Of the 7066 gray spores, 4054 were recombinant while 3012 were non-recombinant. The cross over frequency was 57%. Of the 13946 tan spores, 8277 were recombinant and 5669 were non-recombinant. The cross over frequency was 59%.