Tuesday, August 6, 2019
Nissan Motors Essay Example for Free
Nissan Motors Essay Dramatic loss in 2008 was wake up call for Nissan Motors Head Office, and the CEO of the company has conducted a meeting with fellow managements and shareholders to discuss the recovery plan for the company. As a result, he came up with Five year recovery plan detailed below. 1. Categorise by geographically- they categorised their market into three regions: Americas, Asians, AMIE which includes Africa, Middle East, India and Europe includes Russia. Each regions manufactured car will be sold in the nearby countries, saving transport cost. 2. Change in targeted customers- theres been sale increase in China and India, Nissan focused on selling more cars to those areas instead of the main customers such as USA, by doing that theyre making cars that meets the certain countries, for example in Japan, people buy car to get from A to B, whereas in Europe, people tend to go for money saving cars (eco-friendly/efficient 3. Reducing overall wage bill- means Nissan stopped hiring new staff, cut overtime, and introduced work sharing. Also, they made redundant of 20,000 workers in high cost countries including 1,500 in the UK. In Asia, they temporarily reduced salaries of cooperate officers by 25%, general managers by 20%, and other staff around 15% and eliminated bonuses and compensations. 4. Scrap scheme- In 2009, 10y+ cars can be exchanged for à ¯Ã ¿Ã ½2000 towards their new car. It encouraged people to buy new car to help car manufactures to grow, bring more customers and replaced old cars with new ones. Nissans Scrap Scheme They extended the scheme for drivers exchanging 8-10 year old car to buy any British build range that includes any new Nissan Micra, Nissan Note, Nissan Qashqai. That means some people managed to buy British built Nissan Micra for as little as à ¯Ã ¿Ã ½5,995. CONCLUSIONS From the table above, it is clear that it has been a wake up call for the company. They recognised it quickly and came up with a solution that has worked for them perfectly. According to BBC website, they published that Nissan Motors recovered fully in three years instead of five, which is great news, however they cannot sit back and relax as the global economy is not yet fully recovered and there is a chance that foreign currency might fall and rise anytime again. Press are saying that they recovered, but according to the speech of the CEO of Nissan Motors, hes claiming that they are still in their recovery mode and continuing to watch their expenses and preparing for any event that might come up in the future. BIBLIOGRAPHY www.bbc.co.uk
Monday, August 5, 2019
The Customer Driven Marketing Strategy Marketing Essay
The Customer Driven Marketing Strategy Marketing Essay The marketing strategy explains the companys overall mission statement and future goals. Mostly marketing strategies are set with careful consideration by senior management. Marketing strategy must in cooperate the mission statement of the business. Shankar and Carpenter (2012, p.2) views marketing strategy as a broad plan of managerial initiatives and actions relating an organization to its customers and markets. Further states that there are three key aspects of marketing strategy as follows: Marketing strategy focuses on the strategic decisions necessary to allocate resources. It concerns managerial actions that have long-term effects. Decisions relating to marketing strategy are made by marketing executives in an organization and implemented by many others through the organization and beyond. Following are the four major activities involved in managing a customer-driven marketing strategy and the marketing mix are, i.e. Segmentation Targeting Differentiation Positioning Consumers are the centre of all marketing activity. The basic goals for all businesses are to create value for customers and build a strong profitable customer relationship. As stated by Kotler and Armstrong (2008, p.45) The marketing logic by which the company hopes to create this customer value and achieve these profitable relationships. Since the company owns the means of production it has the overall power to decide which customer to serve (segmentation and targeting) and how it will serve them (differentiation and Positioning). The business identifies the total market, then divides it into smaller segments, selects the most promising segments, and focuses on serving and satisfying customers in these segments in order to secure maximum profit. Using the market strategy the company then designs an integrated marketing mix made of factors under its control .i.e. Product , Place, Price, Promotion The four Ps. In order to find the best marketing strategy the company then uses market analysis, planning, implementation, and control. Through these activities fulfills the changes in demand from consumer behavior and adopts to the marketing environment. As stated by Mullins and Larreche (2006, p.3) IBMs competitive strategy was also quite consistent over the years, Given that the firm was never the lowest-cost producer in the industry, it did not try to compete with low prices. Instead, the firm pursued a quality differentiation strategy by offering superior products backed up by excellent technical service and selling them at premium prices. Customer-Driven Marketing Strategy In order to succeed in the modern competitive marketplace companies need to be customer centered, .i.e. they must fulfill the rapidly changing demands of the customer. Companies must draw the customer from competitor business, make them brand loyal and grow them by delivering greater value. Before anything a company must understand the needs and wants of its customers, only then it can fulfill by using the marketing strategy. Thus the company must use a careful market analysis. Market Segmentation The modern market is full of many types customers, products and needs. The company then determines which demand it can fulfill best and gain maximum benefits. Consumers are grouped in various ways geographic, demographic, psychographic, and products are made to fulfill their needs and wants. As stated by Kotler and Armstrong (2008, p.46) The process of dividing a market into distinct groups of buyers who have different needs, characteristics, or behaviors, who might require separate products or marketing programs is called market segmentation. Market segmentation consists of consumers who adopt in a similar way to different marketing efforts. In the car market for example wealthy consumers own the top notch cars but still make up only one segment of the market. Then we consumers who are price conscious and make up another market segment. It would difficult to fulfill needs of both segmentations so companies focus on the needs of one segment. Market Targeting After a company has defined one of its market segments it can target different segments of consumers. Market targeting involves information of each market segment and then selecting one or more segments to enter. The company must target segments in which it can best fulfill the needs of consumers. Wise companies enter into a segment from which they can achieve success in gaining customer loyalty and sustain it over time. A company might use the strategy niche marketing and target only a few segments from which the major competitor over looked. Alternatively companies might serve different kinds of customers but with the same wants, .i.e. Coca Cola. Multi nationals may serve the needs of all market segments. Most companies enter the market serving only segment of the market but as they gain success they grow and target a range of segments. Companies that attain the most success will eventually have the means necessary to serve all segments of the market; these leading companies have the different product design for each different market segment. Market Differentiation and Positioning After a company has chosen its market segment to enter, it must be decide how it will differentiate its market offering from competitors and must have unique way of serving its chosen target segment in order to secure maximum profits. A products position is the place it has in place of its competitor in the minds of consumers. The position of the product is one of the most crucial things in order to get consumers to buy it and attain brand loyalty from them. If products were similar consumers would have no way of differentiating between products and thus there would be no need to buy it. Positioning is the business securing a unique space in the minds of consumers in comparison to competitors products. When positioning its products the company identifies the plus points it has in that segment that provides competitive advantage over competitor. The company can give greater value to customers at low prices in comparison to competitors and attain a unique position in the market and win consumer brand loyalty. If a company promises greater value then it must differentiate its product from competitors and must deliver greater value in order for the product to maintain position in minds of the consumers. Thus effective positioning begins with differentiation, actually differentiating the product so that it gives consumers more value. When a company has achieved a successful position it must make strong steps to deliver and communicate that position to target consumers. The entire marketing program of a company appreciates the chosen position strategy. Developing an integrated Marketing Mix After developing the market strategy the company begins to plan the details of the marketing mix. The marketing mix a set of controllable marketing tools that the firm uses to produce the response it wants to get back from the target market. The marketing mix is whatever a firm has the power to do in order to influence demand on its product. The marketing mix consists of the four Ps Product, Price, Place, and Promotion. Product means the goods and services combination the company the target market. Price is the amount of money customers would have to pay to obtain the product. Different companies target different range of customers i.e. luxury car makers target the wealthy consumers. Place includes the different locations the companys product is available to target consumers. Promotion means attract consumers and persuades them to buy the product. Ferrell and Hartline (2011, p.17) explains, The role of social responsibility and ethics in marketing strategy has come to the forefront of important business issues in todays economy. Our society still reverberates from the effects of corporate scandals at Enron, WorldCom, and ImClone, among others. Although these scandals make for interesting reading, many innocent individuals have suffered the consequences from these companies unethical behavior.
Alcohol Treatments and Rehabilitation Programs
Alcohol Treatments and Rehabilitation Programs Medical intervention for drug addicts is part of achieving social normalisation. Choose a drug addiction (e.g. tobacco, alcohol, heroin, amphetamine or marijuana). Explore methods of treatment for this drug addiction within medical establishments and problems faced. What are the most effective methods and what might improve success rates of rehabilitation? During the ancient times alcohol consumption was basically used for medical purposes. The use of alcohol is popular in many societies, and its influences differ significantly with consumers. This trend is not only common in adult population, but also in adolescents. Although, it is often difficult to differentiate between casual drinking and alcohol abuse, continuous abuse of alcohol is often influenced by socioeconomic, mental and environmental factors, which can be life-threatening. Furthermore, alcohol can lead to potential physical disabilities and increase risks for social violence.Prolong consumption of alcohol can have harmful effects on the mental health and other important system in the body of consumers. This essay will examine different methods of alcohol treatments used in alcohol addiction such as drug treatment and non-pharmacological treatment. It will argue that the most effective treatment is Naltrexone. In addition, it will also argue that effective behavioural ther apies will improve success rate of rehabilitation for alcohol dependents. In the 19th century, alcohol was popular among the Australians, especially in New South Wales, but during 1980s, alcohol consumption was as low as two Litres per head. On the other hand, it increases to three Litres per head. Since ages ago, alcohol intake was mainly focus in Australian male beer drinking culture. Financial pressures have not been the only influences on drinking patterns but also moral and social changes. As a result to this, many women started consuming alcohol as well and there was drinking culture changes in Australia (National Drug Strategy, 2001). At some point, in 20th century high demand on alcohol lead to change in liquor store close up earlier at six p.m. However, it does not work out as the alcohol dependence addict against this rule. In 1982 alcohol use in Australia was 9.8 Litres per head but it drops to 7.5 per head in 1988 and 1993. The average age group in men that started drinking alcohol is 16 years old to compared with women. An additional, women of all ages consume a smaller amount of alcohol contrast with men or could be non-drinker. Mostly, women like better to drink wine and men regularly choose to drink beer. Binge drinking to intoxication and are common in adolescent. It is defined as having more than seven drinks in male and more than five drinks in female. As a result, binge drink is common between current age group and from community (National Drug Strategy, 2001) There are a number of ways to treat patients with alcohol problems. These include; pharmacotherapy, psychosocial and motivation treatments. The first treatment in alcohol addiction refers to pharmacotherapy. In this therapy, there are three main drugs that are used in treating alcohol, which include; Disulfiram, Naltrexone and Methadone (Caputo, Vignoli, Grignaschi, Cibin, Addolorato, Bernardi, 2014). The first, drug that is used in alcohol treatment is called Disulfiram. It is defined as a quaternary ammonium compound. It has been used in treating alcohol dependency for the last 60 years (Melo, Lopes, Alves, 2014). Disulfiram has shown positive impacts in patients with alcohol dependence even through oral medication are taken (Skinner, Lahmek, Pham, Aubin, 2014). In addition, Disulfiram was the first medication that was approval by Food Drug Administration (FDA) (Elbreder, Humerez, Laranjeira, 2010). However, Disulfiram effectiveness depends on the capability to block the action of acetaldehyde dehydrogenises, which with alcohol ingestion sharply increases the blood absorption of Acetaldehyde according to Zindel Kranzler, (2014). As a consequence, using Disulfiram could cause side effects such as facial flushing,headache and nausea according to Zindel Kranzler, (2014). Furthermore, Melo, Lopes, Alves (2014) claim that alcohol dependent may develop possible reaction after taking Disulfiram for long term such as; fatigue, delirium and also vomiting. Although this medication is frenquently used to treat alcohol patients, it can also react on the central nervous system, which inhibit dopamine as well as increasing dopamine concentration in the metabolic systems (Elbreder, Humerez, Laranjeira, 2010). Hence, when Disulfiram is used appropraitely, it will have positive impact on patientsââ¬â¢ health who have been depending on alohol. Another drug which is used for alcohol treatment is Methadone, which is a synthetic opioid that is used as anti-addiction medication. Methadone is often used for residents with an opioid dependency such as; heroin, oxycodone, hydrocodone, morphine, oxymorphone, fentanyl and many more (Caputo, Vignoli, Grignaschi, Cibin, Addolorato, Bernardi, 2014). Methadone helps to stabilise withdrawal symptoms during detoxification and helps recovering addicts manage their cravings. In addition, methadone is used in alcohol addiction treatment and can either be a short term or a longer term program. It is used to assist the detoxification process, and can help manage symptoms of recovery and support residents in maintaining sobriety. Dyer White (1997) claim that during the intake of methadone there are general side effects such as; insomnia, sweating, painful joints and bones. In addition, it is also claimed that majority of alcohol addicts complain of constipation, dry mouth as well as depressi on, perhaps due to hormonal changes (Dyer White, 1997). According to Petrakis, et al., (2006) patients will also have symptom such as, delirium and anxiety. As a result during the admistration of this medication, patients need to be monitered closely from those symptoms. Thus, methadone is use in alcohol treatment from stopping patient from having craving of alcohol and also helps patient to overcome from alcohol. Another, drug that is used to treat patients with alcohol addictions are also treated with Naltrexone. This is a drug that is given to patients who are dependent on alcohol and is safe for psychiatric disorder patients. In addition, Naltrexone can be administered through two methods, which include patients taking through long-acting injection and the other through oral tablets (Elbreder, Humerez, Laranjeira, 2010; Anton, et al., 2011; Galvez, Fernandez, Manzanaro, 2013). The primary function of Naltrexone primary is to decrease chances of withdrawal symptoms and the cravings of alcohol (Littleton Zieglgansberger, 2010). Furthermore, naltrexone is more effective for a patient with high craving (Elbreder, Humerez, Laranjeira, 2010). According to Mark, Kranzler and Song (2003) Naltrexone it reduces the addictââ¬â¢s desire for alcohol consumption. Also, Caputo, Vignoli, Grignaschi, Cibin, Addolorato, Bernardi ( 2014) state that side effects can be faced by alcohol dependent while on this medication such as, head-aches, nause and anxiety. Another side effect of this drug include; sleep difficulty, irritability and anxiety (Anton, et al., 2011). However, the advantages of using this medication is that, for the duration on this medication treatment, the patient is allowed to consume small amount of alcohol (Anton, et al., 2011). Despite, its side effects, Naltrexone can still have positve impact on alcohol dependents. Thus, Naltrexone is generally given to patients to stop the craving for alcohol, because it can be taken through oral or injection method. Apart from pharmacological treatments, there are two non-pharmacological treatments that can assist patients depending on alcohol. These non-pharmacological treatments include; behavioural therapy and community-based rehabilitation programs. The first treatment refers to behavioural therapies. For example, a counselling and motivational interviewing with alcohol addicts can play an important role to assist patients. The advantage of using this therapy is that, it is implemented outside from health institutions, such as primary care, community centre and school (Kalapatapu, Ho, Cai, Vinogradow, Batki, Mohr, 2014; Feinn, R, Kranzler, 2007). In addition, behavioural therapies are principally successful in giving self confidence, changes for change, and provide the ability for some people to quit drinking on their own (Feinn, R, Kranzler, 2007). On the other hand, financial and organizational resources are generally restricted in alcohol treatment. This means that the treatment is foc used on improving and changing drinking behaviors of alcohol addicts. Also patients, who are staying in countryside, might have difficulties to get medical treatment due to time-consuming, especially to travel from distances to access the rehabilitation services. Such limitations could deny the patient from being treated. Indeed, there was alternative method to treat alcohol addiction patient via telephone, which might not need to be confronting each other, between the medical staff and client. The result from that treatment, using telephone as a technique to communicate with alcohol patient has shown positive response. In contrast, using telephone to talk to alcohol addiction cannot identify where there the patient is going through any sign and symptom such as depression during alcohol withdrawal (Kalapatapu, Ho, Cai, Vinogradow, Batki, Mohr, 2014). In general, it is a good method to treat patient from alcohol withdrawal without worrying even though the patient is in rural area. T he second non-pharmacological treatment involves community-based programs. This treatment focuses on helping alcohol patients from overcoming alcohol habits are through community rehabilitation. It is a treatment utilized to serve patients which have both mental and physical disabilities. For example, a study was done with 65 participants from State-funded vocational rehabilitation agencies to get three or four days for patients to participate in that study (Sprong, E, D, Pappas, Melissa, 2012). The aim of community rehabilitation was to determine that this course could be effective to contribute and identify the barrier in community rehabilitation. However, from this study, 27 patients disagreed to take part in the survey. There were 23 males and 15 females who participated in this study. During the study, patients are asked to answer few question and what are likely symptoms often they encounter while on alcohol, such as vomiting, hand shaking or sleepless night (Sprong, E, D, Pa ppas, Melissa, 2012). Unfortunately, this study was unsuccessful because of patients low education background, but by providing some motivational programs and counseling sessions could help achieve the aims of this community-based program (Sprong, E, D, Pappas, Melissa, 2012). Thus, it is one of the treatments in alcohol patient that could help to live normal life. In conclusion, alcohol is an addictive substance and can lead to many social and mental health problems when abused. However, there are various medical treatments and effective social rehabilitation programs for alcohol addiction that can play an important role to assist in recovery processes of addicts who are struggling to cope with this problem. Effective alcohol treatments and rehabilitation programs will not only reduce the rate of alcohol dependence successfully, but will also prevent other alcohol-related issues in the society. References Anton, R. F., Myrick, H., Wright, T. M., Latham, P. K., Baros, A. M., Waid, L. R., Randall, P. K. (2011). Gabapentin Combined with Naltrexone for the treatment of alcohol dependence. Am J Psychiatry, 709-717. C. B. (2000). Medical Consequences of Alcohol Abuse. alcohol research and health, 27. Caputo, F., Vignoli, T., Grignaschi, A., Cibin, M., Addolorato, G., Bernardi, M. (2014). Pharmacological management of alcohol dependence : From mono-therapy to pharmacogenetics and beyong. European Neuropsychoparmaology, 24, 181-191. doi:http://dx.doi.org/10.1016/j.euroneuro.2013.10.004 Desai, M. M., Rosenheck, R. A., Craig, T. J. (2005). Screening for Alcohol Use Disorders Among Medical Outpatients: The Influence of Individual and Facility Characteristics. The American Journal of Psychiatry, 1521. Dyer, K. R., White, J. M. (1997). Patterns of symptom complaints in methadone maintenance patient. National Drug Strategy Postgraduate Research Scholarship, 1445. Elbreder, M. F., Humerez, D. C., Laranjeira, R. (2010). The use of disulfiram for alcohol-dependent and duration of outpatient treatment. Eur Arch Psychiatry Clin Neurosci, 191-195. Feinn, C. E., R, A. A., Kranzler. (2007). Exploring Treatment Options for Alcohol Use Disorders. National Institutes of Health, 214-221. Galvez, P. B., Fernandez, L. G., Manzanaro, V. M. (2013). Addressing Unhealthy Alcohol Use In Primary Care. New York: Richard Saitz. Hulse, G. K. (2012). Improving clinical outcomes for naltrexone as a management of problem alcohol use. British Journal if Clinical Pharmacology, 632-641. Kalapatapu, R. K., Ho, J., Cai, X., Vinogradow, S., Batki, S. L., Mohr, D. c. (2014). Cognitive-Behavioral Therapy in Depressed Primary Care Patient with Co-Occuring Problematic Alcohol Use : Effect of Telephone-Administered vs. Face-to-Face Treatment -A Secondry Analysis. Journal of Psychoactive rugs, 37-41. Littleton, J., Zieglgansberger, W. (2010). Pharmacological Mechanisms of Naltrexone and Acamprosate in the Prevention of Relapse in Alcohol Dependence. The American Journal on Addictions, 53-61. Mark, T. L., Kranzler, H. R., Song, X. (2003). Understanding US addiction physicians low rate of Naltrexone Prescription. Drug Alcohol Dependence, 71, 219-228. doi:http://dx.doi.org/10.1016/S0376-8716(03)00134-0 Melo, R. C., Lopes, R., Alves, J. C. (2014). A Case of Psychosi in Disulfiram Treatment For Alcoholism. Hindawi Publishing Corporation, 1-4. Petrakis, I. L., Poling, J., Levinson, C., Nich, C., Carroll, K., Ralevski, E., Rounsaville, B. (2006). Naltrexone and Disulfiram in patient with alcohol Dependence and Comorbid Post-Traumatic Stress Disorder. Veterans Affairs MERIT grant (to ILP) and the VISN I Mental Illness Research Education and Clinical Center (MIRECC) (BR), 777-783. Skinner, M. D., Lahmek, P., Pham, H., Aubin, H. J. (2014). Disulfiram Efficacy in the Treatment of Alcohol Dependence : A Meta-Analysis. OPEN ACCESS Freely available online, 16. Sprong, E, M., D, T., Pappas, Melissa. (2012). Utilization of Community Rehabilitation Programs : Screening for Alcohol and Drugs. Journal of Rehabilitation , 13. strategy, N. D. (2001). Alcohol in Australia : Issues and Strategies. Canberra: The National Alcohol Strategy. Zindel, L., Kranzler, H. R. (2014). Pharmacotherapy of Alcohol Use Disorders:Seventy-Five Years of Progress. Journal of Studies on alcohol and drugs/supplement, 79-88.
Sunday, August 4, 2019
John Adams versus John Quincy Adams Essay -- essays research papers
Even though John Adams (1735-1826) and John Quincy Adams (1767-1848) were father and son, also they were our President in the United States but they are not the same. The differences are their early lives, the early political career, and major presidential actions. The early lives of John Adams and John Quincy Adams are different. John Adams?s father, who also named John, sent his son ? young Adams to Harvard College at age fifteen, and he expected him to become a minister. His father was working hard to make young Adams?s life different than his own which was to become an educated person. However, John Adams did not want to become a minister. After he graduated in 1755, he taught school for few years in Worcester, and that allowed him to think about his career choice. After much reflection, he decided to become a lawyer, and studied law in the office of James Putnam, a prominent lawyer in Worcester. In 1758, he was admitted to the bar. He put the skill to good use as a lawyer, often recording cases he observed so that he could study and reflect upon them. His report of the 1761 argument of James Otis in the superior court of Massachusetts as to the legality of Writs of Assistance is a good example. On the other hand, John Quincy?s fat her which is John Adams did not push him to become a minister. Moreover, John Adams brought young Adams to France (1778 ? 1779) and to the Netherlands (1780 ? 1782) to acquire his early education at institutions at the University of Leiden. John Adams let his son explored the world more than his own father did. At age fourteen, young Adams accompanied Francis Dana on a mission to St. Petersburg, Russia, to gain recognition to the new republic. He also spent time in Finland, Sweden, Den... ... appointed him. He felt he deserve credit for helping to set this country on the right path towards freedom, prosperity, and loyalty to the country. Although they might not appreciate it now, his confident future generations will follow his lead to make this country the best it can be. For that generation he could offer this, once you set your goals, never give up. He had numerous jobs as minister and ambassadors to many different countries before he finally won the election to become the President. The path he traveled was not easy, but I think he believed his hard work paid off. I think if he still alive today he would probably take revenge on all those crooked politicians he had been hearing about who take bribes and shred confidential documents. They deteriorate the fabric this country was built on, and it will be a long time before it is fully repaired.
Saturday, August 3, 2019
Lorraine Glass :: essays research papers
Landscape Writing and the Lorrain Glass à à à à à Looking through my Lorrain glass I saw different moods of a scene. I sat on top of my car and looked out over a field of apple trees, raspberry bushes, and pumpkin patches. At the end of the fields was a huge white house with a ton of windows. The house had a wide porch that went all the way around to the back. I couldn't see much detail from such a great distance, but the smoke coming out of the chimney told me there was someone inside. à à à à à I chose three different colors to put into my Lorrain glass. Red, yellow, and green slates of color all gave a different feeling to the picture I was creating in my frame. It was almost like a snap shot. I chose colors that I thought were drastically different to give a different feeling for the same scene. à à à à à Each slate did give a different feeling, but they looked similar in shape. Through the cellophane wrap, when the wind blew, the images seemed to wave. They had a small slant and looked as if they were moving. It was about 4 p.m. and the sun was just going down. The sun would hit the Lorrain Glass and made the image bright. à à à à à The red piece of cellophane made me feel hot. I felt that the sun coming through made it seem even warmer. It gave me a feeling of desert warmth with no water in sight. All the trees looked bare and dead. The yellow piece of paper made everything seem sunny and bright. The house looked full of light. I could picture in my mind the owner of the house having a glass of lemonade on the porch. The trees, the house, and the pumpkins all seem to come to life. They looked full and lively. The green cellophane seemed kind of cold and dark. The sun coming through of course made it seem a little brighter but it still had that sense of dreariness. The pumpkins looked rotted and old, the trees appeared bare with bad apples around its base, and the house just seemed to blend into the back round.
Friday, August 2, 2019
Biology Lab
Labà #1à ? Introductionà toà theà Microscopyà & Observationà ofà Prokaryoticà andà Eukaryotic Cells Introduction Manyà ofà theà cellsà andà organismsà thatà youà willà beà studyingà areà atà theà lowerà limitsà ofà visibilityà ofà lightà microscopes;à therefore,à ità isà extremelyà importantà thatà youà attainà criticalà lightingà andà focussing. Ità isà alsoà importantà toà handleà theà microscopeà competentlyà toà avoidà damagingà eitherà theà microscopeà orà theà preparationà youà areà studying. Evenà studentsà whoà haveà previouslyà usedà microscopesà shouldà readà theà instructionsà carefully. Guideà Biolabo Using a web rowser, go toà theà followingà webà site: http://salinella. bio. uottawa. ca/biolabo/à (youà canà tryà ità fromà home). Underà Microscopyà youà willà findà linksà toà pagesà thatà describeà bothà typeà ofà microscopesà youà willà useà thisà semester,à asà wellà asà howà toà setà upà andà useà them. Ità isà stronglyà recommendedà thatà youà visità theseà pagesà priorà toà attendingà yourà firstà lab. Imageà Jà /à Qcapture Althoughà youà canà makeà allà yourà observationsà byà watchingà directlyà throughà theà oculars,à ità alsoà canà beà doneà onà theà computerà screenà usingà theà digitalà cameraà attachedà toà eachà microscope.Forà that,à youà willà useà theà Imageà Jà programà togetherà withà aà captureà plugin calledà Qcapture. Visità theà labà websiteà toà learnà howà toà useà Imageà Jà (linkà onà theà homepage). Allà observationsà canà beà madeà onà yourà computerà screenà orà inà theà oculars. Eachà methodà hasà itsà advantagesà andà drawbacks;à youà willà haveà toà chooseà whichà oneà ità moreà appropriateà (orà theà oneà youà prefer): Oculars Screen ? Greaterà resolution ? Widerà fieldà ofà view ? Canà shareà observationà withà others ? Moreà comfortableà forà users ? Takeà picturesà whileà observing Lab1à ? Microscopy Theà Compoundà Microscope Onà theà Guideà Biolaboà pageà clickà onà theà CX41à Compoundà Microscopeà linkà thenà onà Partsà andà Function. Thisà willà bringà upà aà labelledà lineà diagramà ofà yourà microscope. Familiarizeà yourselfà withà theà variousà componentsà shownà inà thisà figure. Then,à clickà onà Setupà andà Brightà fieldà alignmentà inà orderà toà knowà howà toà useà andà handleà theà microscope. Now,à locateà yourà compoundà microscopeà inà theà cupboardà belowà theà sinkà ofà yourà workstation. Placeà ità onà theà counterà betweenà the omputerà andà theà endà ofà theà counter. Beà sureà thatà wheneverà youà transportà theà microscope,à ità isà alwaysà keptà upright;à theà ocularà lensà willà fallà outà ifà theà scopeà isà tiltedà orà swung. Evenà thoughà youà donââ¬â¢tà needà theà dissectingà microscopeà rightà now,à takeà ità outà ofà theà cupboardà andà installà ità besideà theà compoundà microscope. Connectà oneà firewireà cableà toà eachà ofà theà camerasà installedà onà topà ofà theà microscopes. Thisà way,à everythingà isà setupà forà furtherà observationsà bothà onà yourà computerà screenà andà throughà theà oculars. Partsà ofà theà compoundà microscopeTheà microscopeà consistsà ofà aà systemà ofà lenses,à aà lightà source,à andà aà gearedà mechanismà forà adjustingà theà distanceà betweenà theà lensà systemà andà objectà beingà observed. Thereà areà aà numberà ofà importantà componentsà andà ità isà essentialà thatà youà beà ableà toà identifyà themà andà understandà theirà functionà beforeà youà canà proceed. Byà goingà throughà theà differentà modulesà inà Biolaboà andà usingà theà microscopeà youà willà developà aà competencyà forà brightà fieldà microscopy. Identifyà theà followingà componentsà usingà Biolaboà (Partsà andà functionsà figure)à andà yourà microscope:REVOLVINGà NOSEPIECE:à Supportsà theà variousà objectivesà ? Youà willà onlyà useà theà 4x,à 10xà andà 40xà objectivesà inà theà BIO1140à labsà (notà theà 100x). STAGE:à Supportsà theà specimenà beingà observed. Aà systemà ofà knobsà onà theà sideà ofà theà stageà allowsà youà toà moveà theà specimenà underà theà objectiveà onà theà Xà andà Yà axes. Tryà andà moveà theà stage. COARSEà FOCUSà KNOB:à Permitsà rapidà changeà inà distanceà betweenà theà specimenà andà theà objectiveà therebyà allowingà forà roughà focussingà ââ¬âà Doà notà useà whenà focusingà withà theà 40xà objectiveFINEà FOCUSà KNOB:à Permitsà smallà changesà inà distanceà betweenà theà specimenà andà theà obje ctiveà andà therebyà allowsà forà finalà focussingà ofà theà image. 10 Lab1à ? Microscopy OCULARà ORà EYEPIECE:à Aà magnifyingà elementà inà theà microscope,à usuallyà 10X. Ità isà throughà theà ocular,à orà eyepieceà thatà oneà looksà atà theà specimen. Allà ourà microscopesà areà parfocal,à soà thatà whenà anà objectà isà inà focusà withà oneà objective,à theà focusà willà notà beà completelyà lostà whenà changingà toà theà nextà objective. OBJECTIVES:à Theà magnifyingà elementà whichà isà closestà toà theà specimen.Seeà figureà 1à toà findà outà aboutà theà engravingsà onà theà sideà ofà eachà objective. CONDENSER:à Systemà ofà lensesà thatà concentratesà theà lightà furnishedà byà theà illuminator. Ità doesà notà magnif yà theà object. CONDENSERà HEIGHTà ADJUSTMENTà KNOB:à Allowsà oneà toà focusà theà concentratedà lightà ontoà theà specimen. APERTUREà IRISà DIAPHRAGM:à Usedà toà reduceà glareà fromà unwantedà lightà byà adjustingà theà angleà ofà theà coneà ofà lightà thatà comesà fromà theà condenser; Productionà ofà Imageà byà aà Compoundà Microscope Theà mostà importantà partà ofà aà microscopeà isà theà objective.Allà theà otherà partsà ofà theà instrumentà areà designedà toà helpà theà objectiveà produceà theà bestà possibleà image. Theà bestà imageà isà notà theà largest;à ità isà theà clearest. Thereà isà noà valueà toà aà highà magnification. Ifà theà resolutionà isà poorà youà willà haveà noà betterà understandingà ofà theà specimen. lightà beam ocularà lens Magnification Numericalà apertureà (NA) Determinesà theà resolving powerà ofà theà objective* Opticalà tubeà lengthà /à max. coverslipà thicknessà inà mm prism objectiveà lens specimen condenserà lens Figureà 1:à Objectivesà engravings lightà sourceFigureà 2:à Imageà productionà inà aà compoundà microscope. 11 Lab1à ? Microscopy *Resolvingà powerà isà theà abilityà toà seeà twoà objectsà thatà areà veryà closeà asà twoà separateà objects. Theà humanà eyeà willà resolvingà powerà isà aboutà 100à µm. Usingà theà compoundà microscope Alwaysà handleà theà microscopeà GENTLY! Ità isà anà expensive,à delicateà andà heavyà instrument. Carryà ità withà twoà hands,à oneà handà onà theà arm,à andà theà otherà handà underà theà base. Ifà theà ocularà orà objectiveà isà dir ty,à wipeà ità cleanà usingà ONLYà Kimwipesà orà specialà lensà tissueà andà cleaningà fluidà supplied.Ifà youà useà anythingà elseà youà mayà scratchà theà lens. Wipeà upà anyà cleaningà fluidà immediately;à otherwiseà ità willà dissolveà theà glueà whichà holdsà theà lensà inà place. REMEMBER,à yourà demonstratorà isà hereà toà help,à soâ⬠¦ ASK! 1. Makeà sureà thatà theà powerà cordà isà pluggedà intoà theà backà ofà yourà microscopeà andà intoà aà powerà outlet. 2. Usingà theà letterà ââ¬Å"eâ⬠à microscopeà slideà provided,à followà stepsà 2à throughà 13à inà theà Setupà andà Brightà fieldà alignmentà procedureà ofà Biolabo. Remember,à observationà canà beà doneà onà screenà orà throughà theà oculars. Orientationà an dà workingà distance . Startingà yourà examinationà withà theà 4Xà objective,à positionà theà letterà ââ¬Å"eâ⬠à slideà onà theà stage. 2. Drawà whatà youà seeà inà theà microscope:_________________ 3. Whatà wouldà aà slideà withà theà letterà ââ¬Å"tâ⬠à lookà likeà underà theà microscope? _________________ 4. Usingà theà knobsà locatedà onà theà sideà ofà theà stageà andà lookingà throughà theà microscope,à moveà theà slideà slowlyà toà theà right,à thenà toà theà left. Recordà yourà observations. ___________________________________à 5. Now,à moveà theà slideà slowlyà awayà fromà you,à thenà towardsà youà whileà observingà throughà theà microscope.Recordà yourà observationsà ____________________________________ 6. Focusà onà theà slideà atà 10X. Checkà theà dist anceà betweenà theà objectiveà lensà andà yourà slideà (=à theà workingà distance,à seeà alsoà theà referenceà atà theà endà ofà thisà chapter). Nowà switchà toà theà 40Xà objectiveà andà checkà theà workingà distance. Whatà happensà toà theà workingà distanceà asà yourà magnificationà increases? 12 Lab1à ? Microscopy Depthà ofà fieldà (depthà ofà focus) Lensesà haveà aà depthà ofà focus. Ità isà theà numberà ofà planesà inà whichà anà objectà appearsà toà beà inà focus.Extendà yourà fistà atà armââ¬â¢sà lengthà inà frontà ofà youà andà holdà yourà thumbà up. Concentrateà onà yourà thumbà andà noticeà thatà theà objectsà pastà yourà thumbà onà theà otherà sideà ofà theà roomà areà notà clearlyà seen. Similarlyà withà aà microscope,à whenà ità isà focussedà onà oneà surface,à theà surfacesà lowerà orà higherà willà beà outà ofà focus. 1. Positionà aà preparedà slideà withà colouredà threadsà uponà theà stage. Atà lowà power,à 4X,à focusà onà theà areaà whereà theà threadsà cross. 2. Usingà theà fineà focusà adjustment,à focusà upà andà downà slowly. 3. Repeatà usingà differentà objectives.Whatà canà youà sayà aboutà theà depthà ofà fieldà atà differentà magnifications? Hasà ità increasedà orà decreased? (i. e. ,à canà youà seeà moreà threadsà inà oneà focalà planeà atà 4Xà orà 40X? ) ____________________________________________________________ Magnification Theà magnificationà givenà byà objectivesà andà ocularsà isà engravedà onà them. Theà totalà magnificationà forà anyà combinationà ofà objectiveà andà ocularà isà theà productà ofà theà magnificationà ofà eachà lens. Objectiveà magnification Ocularà magnification Totalà Magnification Lightà intensity Workingà distance 4x 10x 40x High 22mm 10x 10x 100xMedium 10. 5mm 40x 10x 400x Low 0. 56mm Table1à . Comparisonà magnification,à workingà distanceà andà brightnessà atà threeà differentà objectiveà magnifications. Youà alsoà canà calculateà theà magnificationà ofà yourà pictureà usingà theà followingà formula: Magnificationà factor=à measuredà sizeà ofà objectà =à (à à à à à à à à à à à à à X) Actualà sizeà ofà object 13 Lab1à ? Microscopy Specimenà sizeà andà Magnificationà of theà picture Beforeà youà startà thisà exercise,à makeà sureà youà haveà carefullyà readà theà websiteà sectionà rele vantà toà theà softwareà youà willà useà toà takeà digitalà picturesà (ImageJ/Qcapture).Theà goalà ofà thisà sectionà isà toà teachà youà differentà techniquesà thatà willà allowà youà toà determineà theà sizeà ofà objectsà youââ¬â¢reà observingà underà theà microscope. Theà generalà principleà isà fairlyà simple:à 2à objectsà haveà theà sameà relativeà sizeà (expressedà asà aà ratio)à inà theà realà worldà andà underà theà microscope. actualà sizeà ofà objectà Aà à à =à on? screenà sizeà ofà objectà Aà à ? A1à =à A2à à actualà sizeà ofà objectà Bà à à à à à on? screenà sizeà ofà objectà Bà à à à à à à à à B1à à à à B2 Theà followingà exercisesà areà applicationsà ofà thisà formula. Placeà aà sli deà underà theà microscope.Chooseà theà rightà objectiveà andà adjustà theà focusà andà lightà level. Then,à chooseà aà structureà youà wantà toà measureà andà takeà aà picture. A? Firstà method:à Measuringà anà objectà usingà theà fieldà ofà viewà (FOV): Theà simplestà wayà toà determineà theà sizeà ofà anà objectà isà toà useà theà knownà sizeà ofà theà wholeà fieldà ofà viewà (FOV,à theà wholeà pictureà fromà leftà toà right). 1? Onà theà computerà screenà (usingà aà rulerà andà withoutà writingà anythingà ofà theà screen),à measureà theà objectà ofà whichà youà wantà toà determineà theà sizeà (=à A2) 2? Then,à measureà theà widthà ofà theà wholeà pictureà onà theà screenà (=B2). ? Referà toà tableà 2à onà pageà 20à toà knowà theà actualà sizeà ofà theà fieldà ofà viewà forà theà objectiveà youââ¬â¢reà usingà (=B1) 4? Useà theà followingà formula: Actualà sizeà ofà theà objectà (A1)à =à Actualà sizeà ofà theà FOVà (B1)à à à à à xà à à on? screenà sizeà ofà theà objectà (A2) on? screenà sizeà ofà theà FOVà (B2) Example:à Onà aà snapshotà usingà theà 4xà objective,à anà insectà hasà anà on? screenà lengthà ofà 10cm. Theà wholeà pictureà isà 20cmà wide. Whatà isà theà actualà sizeà ofà theà insect? ______________________________ 14 Lab1à ? Microscopy B? Secondà method:à Measuringà anà objectà usingà aà scaleà barà file:Fromà Imageà Jà (usingà theà fileà /à openà command),à openà theà fileà thatà containsà theà relevantà scaleà barà inà the à (T:/BIO/BIO1140):à new10X. jpgà forà theà 10xà objective,à andà new40X. jpgà (forà theà 4xà andà 40xà objectives). Then,à usingà aà rulerà measureà theà followingà distancesà directlyà onà theà computerà screen: 1? Theà on? screenà lengthà (orà width)à ofà theà objectà whoseà sizeà youà wishà toà determineà (=A2) 2? Theà widthà ofà theà scaleà barà onà theà screenà (=B2)à Youà nowà canà calculateà theà actualà sizeà ofà theà objectà usingà theà formula: actualà sizeà ofà objectà =à on? creenà lengthà ofà objectà à xà à actualà sizeà ofà scaleà bar*à à à à à à à à à à à à à à à à à à à à à à à à à à à à à à à à à à à à à à à à à à on? screenà lengthà ofà scaleà bar ?à à à à A1à =à A2à xà B1 B2 *Theà actualà sizeà ofà theà scaleà barà isà indicatedà onà theà scaleà barà fileà (ex:à onà theà new10x. jpgà file,à theà barà representsà 0. 2mmà atà 10xà orà 0. 02mmà atà 100x)à =à B1 Example:à Ià tookà aà pictureà ofà aà smallà insectà larva,à usingà theà 4xà objective. Theà larvaà lengthà isà 60mmà onà theà screen. Theà scaleà barà onà theà new40x. jpgà isà 30mmà andà representsà 0. 2mm. Whatà isà theà actualà sizeà ofà theà larva? _________________________Doà notà putà theà compoundà microscopeà backà inà theà cupboardà youà willà needà ità laterà thisà afternoon. Pointsà toà rememberà concerningà microscopes 1. Alwaysà workà withà aà cleanà microscope. Useà onlyà theà lensà paperà provided. Don'tà forgetà toà cleanà theà slideà too! 2. Alwaysà locateà theà specimenà underà lowà powerà andà workà yourà wayà upà toà theà highà powerà objective. 3. Neverà useà theà coarseà focusingà knobà whenà theà highà powerà lensà isà inà position. Useà onlyà theà fineà focusà knob. 4. Neverà useà theà 100xà inà 1stà yearà labsà (weà didnââ¬â¢tà teachà youà how)à 5.Alwaysà readjustà illuminationà wheneverà youà changeà theà objective. Tooà muchà lightà willà giveà youà aà blurryà imageà thatà youà cannotà focusà on. 15 Lab1à ? Microscopy Theà stereoscopicà microscope (dissectingà microscope) Theà stereoscopicà microscope,à alsoà calledà stereoscopeà orà dissectingà microscope,à isà usedà toà viewà objectsà thatà areà tooà largeà orà tooà thickà toà observeà underà theà comp oundà microscope. Stereoà microscopesà areà alwaysà equippedà withà twoà ocularsà producingà aà stereoscopicà orà three? dimensionalà image. Unlikeà theà compoundà microscope,à theà imageà isà notà inverted.Ourà stereoà microscopesà provideà magnificationà inà theà rangeà ofà 6. 7Xà ? 45Xà usingà aà zoom? typeà lensà system. Byà rotatingà aà dialà locatedà onà theà rightà sideà ofà theà stereoà microscopeà head,à theà viewerà obtainsà aà continuousà changeà ofà magnification. Ourà stereoà microscopesà canà beà usedà withà reflectedà orà transmittedà light. Reflectedà lightà isà directedà untoà opaqueà specimensà fromà aboveà andà isà reflectedà toà theà viewer. Transmittedà lightà isà usedà withà translucentà specimensà andà passesà throughà theà specimenà fromà beneathà theà stageà andà intoà theà viewer'sà eyes.Useà ofà theà stereoscopicà microscope 1. Onà theà Biolaboà homeà pageà leftà clickà onà Stereoscopeà (Dissectingà microscope)à andà thenà onà Stereoscopeà setup. 2. Clickà onà Stepà 1à andà readà ità carefully. Obtainà aà stereoà microscopeà fromà theà sameà cupboardà asà yourà compoundà microscopeà ifà youà havenââ¬â¢tà yet. 3. Clickà onà andà readà stepsà 2à throughà 7. 4. Placeà aà coinà onà theà stage. 5. Usingà theà focussingà knobà onà eitherà sideà ofà theà arm,à lowerà orà raiseà theà objectiveà untilà theà coinà isà inà focus. Examineà ità inà bothà reflectedà andà transmittedà light.Whichà isà bestà forà anà opaqueà specimen? Tryà t heà variousà magnificationsà byà turningà theà zoomà knob. Theà reflectedà light sourceà isà similarà toà aà spotlightà andà itsà orientationà canà beà adjustedà manually. Tryà rotatingà theà lightà upwardsà andà downwards. 6. Examineà otherà materialsà suchà asà brineà shrimpà larvaeà (Artemia)à inà aà watchà glassà usingà bothà reflectedà andà transmittedà light. Addà 1? 2à dropsà ofà ââ¬Å"proto? slowâ⬠à solutionà toà slowà downà theà larvae. Estimateà theà actualà sizeà ofà oneà larva:à __________ 16 Lab1à ? Microscopy Prokaryoticà andà Eukaryoticà cellsItà hasà longà beenà recognizedà thatà livingà organismsà areà composedà ofà basicà structuralà andà functionalà unitsà calledà cells. Cellsà canà beà dividedà intoà twoà generalà type s:à prokaryoticà andà eukaryotic,à basedà onà theà presenceà ofà aà nucleusà andà otherà membraneà boundà organellesà inà theà latter. Prokaryoticà cellsà belongà toà 2à bigà groups:à archaeaà andà eubacteria. Theyà areà usuallyà smallerà thanà eukaryoticà cellsà (typicallyà 1? 5à µm). Theseà unicellularà organismsà mayà beà small,à butà theyà areà theà mostà abundantà organismsà onà theà planet,à representingà aboutà halfà theà biomassà (Biology,à Brookerà età al. 010,à McGraw? Hill&Ryerson). Theyà areà devoidà ofà membraneà boundà organelleà suchà asà theà nucleus,à mitochondriaà orà chloroplasts. Theirà geneticà materialà isà usuallyà composedà ofà oneà circularà chromosomeà plusà otherà extraà chromosomalà elementsà calledà plasmids. Euka ryoticà cellsà areà usuallyà muchà larger. Theyà possessà aà membraneà boundà nucleus,à theirà organellesà areà moreà complexà andà numerous,à andà theirà genomeà isà largerà thanà prokaryotes. Eukaryoticà organismsà canà beà uni? orà multicellular. Youà willà haveà aà chanceà toà observeà manyà eukaryoticà cellsà duringà thisà semester:à Amoeba,à Lilly,à Whitefishâ⬠¦.Inà today'sà exerciseà youà willà takeà aà firstà lookà atà theà similaritiesà andà differencesà betweenà prokaryoticà andà eukaryoticà cellsà asà wellà asà theà diversityà withinà theseà groups. Youà shouldà familiarizeà yourselvesà withà aà wholeà arrayà ofà cellularà structuresà andà organellesà youà willà probablyà encounterà duringà theà courseà ofà thisà exercise. Beforeà yourà scheduledà labà session,à writeà downà theà definitionà andà functionà forà eachà ofà theà followingà terms:à plasmaà (cell)à membrane,à cellà wall,à protoplast,à cytoplasm,à vacuoles,à nucleus,à nucleolusà andà chloroplasts.Eukaryoticà Cells:à Elodeaà (plant) 1? Getà aà youngà greenà Elodeaà leafà fromà theà jar. Mountà ità inà aà dropà ofà waterà onà aà cleanà microscopeà slideà withà theà convexà sideà ofà theà leafà uppermost. Coverà theà preparationà withà aà coverslip. 2? Observeà theà preparationà atà 4X,à thenà atà 10X. Ifà youà seeà brownishà ovalà structuresà onà theà leafà surface,à ignoreà then. Theseà areà probablyà epiphyticà diatoms. Concentrateà yourà attentionà onà theà cellsà nearà theà cent ralà ribà atà theà baseà ofà theà leafà andà onà theà marginalà cellsà atà theà edgeà ofà theà leaf. Canà youà distinguishà severalà layersà makingà upà theà leaf? ____ ? Whatà isà theà averageà lengthà ______à andà widthà ______à ofà theà cellsà inà micrometres? 17 Lab1à ? Microscopy 3? Focussingà atà 40Xà locateà theà cellà wall,à theà vacuole,à theà cytoplasmà andà theà numerousà greenà chloroplasts. ? Whatà importantà biologicalà processà takesà placeà inà theà chloroplasts? _____________________________________ ? Whatà pigmentà isà responsibleà forà theirà greenà colouration? ________________________________________________ ? Whatà isà theà shapeà ofà chloroplasts? ____________________________________________ ? Areà theà chloroplastsà moving? Whatà sortà ofà movement? ____________________________ _____________________ ? Theà phenomenonà youà areà observingà isà calledà cytoplasmicà streamingà orà cyclosis. Whatà doà youà thinkà theà functionà ofà suchà aà processà couldà be? ___________________________________________________ 4? Youà haveà probablyà realisedà thatà theà plasmaà membraneà cannotà beà seenà inà plantà cells. Ità isà tooà thinà toà beà resolvedà withà theà compoundà microscope.Inà orderà toà seeà theà trueà limitingà boundaryà ofà theà cytoplasmà ità isà necessaryà toà treatà theà cellsà inà suchà aà mannerà thatà theà plasmaà membraneà becomesà withdrawnà awayà fromà theà rigidà cellà wall. Thisà canà beà doneà byà placingà theà cellà inà aà strongà saltà solution. Thisà willà causeà waterà toà diffuseà outà ofà theà cellà byà osmosis,à therebyà decreasingà theà cellà volume. Theà unaffectedà cellà wall remainsà inà itsà originalà state. Whatà canà thenà beà seenà isà aà spaceà betweenà theà cellà wallà andà theà limitingà boundaryà ofà theà protoplastà (theà cellà minusà theà cellà wall)à whichà therebyà becomesà visible. Removeà yourà Elodeaà slideà fromà theà microscopeà stage. Delicatelyà removeà theà coverslip,à addà oneà dropà ofà 5%à NaClà solutionà thenà putà backà theà coverslipà onà yourà preparation ? Refocusà atà 40xà (don'tà forget:à youà mustà firstà focusà atà 4X,à thenà 10Xà andà finallyà atà 40x). ? Areà theà cellsà plasmolyzed? (Ifà notà waità aà whileà longer). Howà doà theyà lookà likeà now? __ ____________________ ? Hasà theà cellà wallà beenà affected? _________________à ? Whatà becomesà ofà theà largeà centralà vacuoleà duringà plasmolysis? ______à _______________________________________________ Takeà aà pictureà ofà aà plasmolyzedà Elodeaà cell. Howà doesà ità compareà toà theà previousà picture? 18 Lab1à ? Microscopy Prokaryoticà Cells:à Lyngbyaà (eubacteria:à cyanobacteria)à 1. Takeà aà closeà lookà atà theà sampleà inà theà jar. Whichà colourà wouldà bestà describeà itsà appearance? ___________________ 2. Prepareà aà wetà mountà ofà freshà Lyngbyaà byà theà followingà procedure:à ? Withà forcepsà orà anà eyeà dropper,à putà aà veryà smallà amountà ofà greenà matterà onà aà cleanà slide ? Addà aà dropà ofà waterà fromà theà jar. ? Carefullyà placeà aà co verslipà overà it. Makeà sureà ità liesà flatà onà theà preparation.Don'tà worryà ifà thereà areà justà aà fewà airà bubbles. Withà practice,à yourà skillsà willà improve. However,à ifà tooà manyà airà bubblesà areà present,à yourà preparationà risksà toà dryà outà veryà quicklyà duringà viewing,à compromisingà yourà observations. 3. Startingà withà theà 4Xà objective,à focusà onà yourà preparation. ? Canà youà seeà numerousà greenà filaments? _______ ? Areà theà filamentsà moving? __________ 4. Switchà toà theà 10Xà thenà theà 40Xà objectiveà andà focusà usingà theà fineà focusà knobà only: ? Doà youà seeà theà individualà cellsà makingà upà eachà filament? ________ ? Estimateà theà widthà ofà oneà filamentà inà micrometres:_______ Whatââ¬â¢sà theà filamentà widthà inà millimetresà (mm)? ________ ? REMEMBER:à Youà areà workingà withà livingà cells. Workà quicklyà andà keepà yourà specimenà wetà atà allà times. Dead,à dryà orà damagedà biologicalà preparationsà areà useless. Returningà theà microscopesà afterà use Afterà completingà allà observations,à turnà andà clickà theà lowà powerà objectiveà (4X)à onà theà compoundà microscopeà intoà position. Removeà theà slideà fromà theà stageà andà returnà ità toà itsà correctà box. Wipeà theà stagesà withà aà cleanà paperà towel. Carefullyà disconnectà theà cameraà fromà theà firewireà cable.Makeà sureà youà turnedà offà theà lightà onà eachà microscope,à thenà unplugà theà powerà cordà andà makeà aà looseà coilà ofà ità aroundà theà eyepieces. Returnà theà microscopeà inà theà cupboard. 19 Lab1à ? Microscopy TAsà willà checkà thatà youà properlyà returnedà theà microscopesà inà the cupboardà withà theà cordà properlyà attachedà andà noà slideà presentà onà theà stage. Youà willà loseà marksà forà thisà labà (andà otherà labs)à ifà youà donââ¬â¢tà doà so. Evaluation Aà shortà quizà onà microscopeà components,à specimenà observationsà andà measurementà ofà objectsà willà takeà placeà atà theà beginningà ofà Lab2.Beà onà time,à theà quizà willà startà atà 2:30. References: 1? Metricà systemà (seeà alsoà appendixà IVà atà theà endà ofà labà manual):à 1à centimetreà cmà =à 10? 2à metresà (m) 1à millimetreà mmà =à 10? 3à metres 1à micrometreà ? mà =à 10? 6à metres 1à nanometreà nmà =à 10? 9à metres 2? Sizeà ofà cameraà fieldà ofà viewsà (fov): Tableà 2:à Fieldsà ofà View:à Olympusà CX41à Compoundà Microscopeà Objective 4X 10X 40X 100X Cameraà fieldà ofà view (widthà inà mm) 1. 75 0. 70 0. 175 0. 070 Tableà 3:à Fieldsà ofà Viewà ââ¬âà Olympusà SZ61TRà Dissectingà Microscopeà Zoomà Setting 0. 67X 0. 8X 1X
Thursday, August 1, 2019
Belonging – ‘We Are Going’
What does the Oodgeroo Noonuccal poem ââ¬ËWe Are Goingââ¬â¢ have to say about Belonging and Not Belonging? How does the poet use language forms, features and structures to convey ideas and feelings? The poem ââ¬ËWe Are Goingââ¬â¢ by Oodgeroo Noonuccal is about the displacement of the Aboriginal people in Australian society/culture and their confusion about where or what to belong to as their traditional customs are taken away/forgotten. The text raises the issues and themes of ââ¬ËBelongingââ¬â¢ through a mostly-ââ¬Ëdefeatedââ¬â¢ tone as it shows their loss of tradition and culture in the new Australia.In order to create a sense of sympathy and consideration for the Aboriginal people, the poet uses a range of language forms and techniques to cause effect in this text. One of the most important of these is the writerââ¬â¢s use of Irony ââ¬â in Lines 8-9 we see the words, ââ¬Å"We are strangers here now, but the white tribe are the strangers. We belong h ere, we are of the old waysâ⬠. This statement, in particular, expresses the overall message of this poem while focusing on the ââ¬ËBelongingââ¬â¢ concept.The writer put forward the interesting yet tragic idea that the Aboriginal people no longer belong to their homeland, whereas the ââ¬Å"White tribeâ⬠ââ¬â who are unable to fully understand or appreciate it as the Indigenous do ââ¬â have now overrun them and belong more to this land now than they do. This side of the poem brings it its tragic and ââ¬Å"defeatedâ⬠tone, thus affecting the reader. The language the poet uses is quite informal and colloquial, without using any slang. The feeling created is that of a story-telling almost.They also use some Indigenous words such as ââ¬Å"corroboreeâ⬠and ââ¬Å"Dream Timeâ⬠. This is in-keeping with the poetââ¬â¢s heritage and the nature of ââ¬Ëbelongingââ¬â¢ to a language and to a people. Using unusual, broken-meter and irregular phrasin g, the melancholy mood is heightened in that it doesnââ¬â¢t flow as a poem often does. This puts more emphasis on each line and makes it sound less like a poem, more like a short story. Then, in Lines 8-14, the constant repetition of the word ââ¬Å"weâ⬠at the beginning of each line gives the poem a more defiant, hopeful edge; making it sound like a pledge.The blunt contrast between the words ââ¬Å"Weâ⬠and ââ¬Å"Theyâ⬠at the beginning of many lines de-humanises the White people, making them seem more like an enemy or foe. The poet also uses very emotive words such as ââ¬Å"Subdued and Silentâ⬠, ââ¬Å"Dream Timeâ⬠, ââ¬Å"Laughterâ⬠and ââ¬Å"Belongâ⬠to cause effect, as well as Visually-impacting words such as ââ¬Å"Wandering Camp Firesâ⬠, ââ¬Å"Lighteningâ⬠, ââ¬Å"Dark Lagoonâ⬠and ââ¬Å"Shadow Ghostsâ⬠. These add to the emotional effect and eerie feel. Like a true Indigenous person (the author is clearly Aborigi nal by looking at her name and her use of ââ¬Å"theyâ⬠and ââ¬Å"weâ⬠), they speak of the land like their mother, their provider (eg. The shrubs are gone, the hunting and the laughter. The eagle is gone, the emu and the kangaroo are gone from this placeâ⬠, and so the poet asserts a strong connection and sense of ââ¬ËBelongingââ¬â¢ to the land and to their people, even though they are ââ¬Å"dying outâ⬠as a culture and community. As the final line states, ââ¬Å"And We Are Goingâ⬠, the writer is not only stressing that their race or clan is becoming extinct, but also that the traditional Indigenous customs and traditions and being forgotten.These are a part of the Aboriginal culture and a significant thing, which they belong to as a people. This is shown through the writerââ¬â¢s emphasis on these customs and traditions in such lines as ââ¬Å"We are the corroboree and the bora groundâ⬠and ââ¬Å"We are the wonder tales of the Dream Time, the tribal legends told. â⬠When the poet uses phrases like ââ¬Å"The Shrubs are goneâ⬠and ââ¬Å"The emu and kangaroo are gone from this placeâ⬠, she doesnââ¬â¢t mean they are extinct completely, of course.What she is saying is, in fact, is that their traditional way of life is gone ââ¬â the hunting and gathering, their ââ¬Å"wandering camp firesâ⬠. The White people have come and taken over their land and have chased away many of the native plants, animals etc. and as such the Aboriginals are left confused and misplaced in their own land, becoming dependent on the Europeans for food, whereas before they were self-sufficient and able to hunt, and medicine, with the introduction of virus and disease.And so, basically, the poem is in fact a metaphor for the disappearing old way of life of the Aboriginal people and their connection and sense of Belonging to the land. It assumes a slightly nostalgic tone with traces of defiance in some parts but an overall sen se of hopelessness and defeat. Through it, we the reader meditate on the idea of ââ¬ËBelongingââ¬â¢ and ask ourselves what the Aboriginal people will belong to in our society where their old traditional ways are being taken away. In the words of Oodgeroo Noonuccal, ââ¬Å"We Are Goingâ⬠.
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