Boss Appreciation Day Quotes

Here is an unofficial code: if you want to climb the corporate ladder, first learn to manage your boss. With a happy boss, you can reach the top. On this Bosss Day, share these quotes with your superior to win them over. Robert Frost The difference between a job and a career is the difference between forty and sixty hours a week. Sam Walton There is only one boss. The customer. And he can fire everybody in the company from the chairman on down, simply by spending his money somewhere else. Howard Aiken Dont worry about people stealing your ideas. If your ideas are any good, youll have to ram them down peoples throats. John Gotti If you think your boss is stupid, remember: you wouldnt have a job if he was any smarter. Lawrence H. Martin In many businesses, today will end at five oclock. Those bent on success, however, make today last from yesterday right through to tomorrow. Elbert Hubbard There is no failure except in no longer trying. Doug Larson Accomplishing the impossible means only that the boss will add it to your regular duties. Casey Stengel The secret of successful managing is to keep the five guys who hate you away from the four guys who havent made up their minds. The key to being a good manager is keeping the people who hate you away from those who are still undecided. Peter Drucker Management by objective works—if you know the objectives. Ninety percent of the time you dont. Homer Simpson Kill my boss? Do I dare live out the American dream? Tim Gould Ive been promoted to middle management. I never thought Id sink so low. Byron Pulsifer A good boss is a person who can tolerate my complaints and still manage to say hello to me every day. If it wasnt for bad bosses, I wouldnt know what a good one was like. Leo J. Farrell, Jr. The mark of a true executive is usually illegible. Cedric Adams Executive: A man who talks to visitors so the other employees can get their work done.

Ethnic Tensions Between The Rwanda And The Rwandan Economy

Introduction For decades, Rwanda had been griped with ethnic tensions between the majority Hutu and minority Tutsi populations. These tensions culminated in 1994 when 800,000 to 1 million Tutsis and moderate Hutus were killed by Hutu extremists. It is known to be â€Å"the most efficient mass killing since the atomic bombings of Hiroshima and Nagasaki.† While the ethnic tensions between the Hutus and Tutsis has been cited as the root cause for the genocide, it was not the only reason. It was the economic and political instability that plagued the nation coupled with the ongoing ethnic tensions that led to the genocide in 1994. Pre-Genocide Rwandan Economy Overview Before the genocide in 1994, 90% of the Rwandan population relied on rain-fed subsistence agriculture, which accounted for around 38% of total GDP. Agribusiness also accounted for about 70% of exports, with coffee and tea as the major sources of export earnings. With few natural resources, Rwanda’s economy was mainly restricted to small and uncompetitive industrial sectors, and the production of coffee and tea was especially suited to the small-farm size and family-based mode within the nation. As an economy highly dependent on export earnings, Rwanda’s main export products, such as coffee, were cultivated by around 70% of rural households through the country. In fact, the economic crisis occurred in Rwanda in the early 1990s was mainly attributed to the collapse of international coffee market and furtherShow MoreRelatedThe Genocide Of The Rwandan Genocide1421 Words   |  6 PagesThe Rwanda Genocide was an unfortunate case where thousands of deaths could have been prevented, but because of irresponsibility and selfishness of global governments’ innocent lives were lost. 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And lastly, how justice was delivered. pective The Rwandan Civil War The Rwandan Civil War was a conflict between the government of President Juvenal Habyarimana and the rebel Rwandan Patriotic Front (RPF) in Rwanda.The conflict began on 1 OctoberRead MoreUNs Failures in Preventing Rwandan Genocide811 Words   |  3 PagesAldelman (2005), the Rwanda 1994 genocide was the most disastrous case of mass murder the entire world has ever witnessed since WWII. The genocide resulted from the deliberate choice of a modern elite to foster hatred and fear to keep itself in power. According to Shah, (2006), this was a case of the majority Hutu who comprised 85% of the population turning against the Tutsi minority who made up 12% of the population in order to counter a growing political opposition within Rwanda. The killings accountedRead More Roots of the Rwandan Genocide1739 Words   |  7 PagesApril 6, 1994, Rwanda experienced a period of great turmoil as thousands of people fell victim to the horrors of the Rwandan genocide. The main targets of the genocide were Tutsis and Hutu moderates. Though the main cause of the genocide was a conflict between two ethnicities, the genocide was also fueled by political factors and social conditions. Rwanda is the smallest sub-Saharan country with a population of about 7 million inhabitants. Although the indigenous peoples of Rwanda are the Twa, theyRead More Civil War in Congo Essay1690 Words   |  7 Pages nbsp;nbsp;nbsp;nbsp;nbsp;The recent Civil War in Congo has been a bloody flight, causing more then 3.3 million deaths in just 4 short years.1 Various rebel and ethnic groups have have been involved in the violence, fighting over Congos rich natural resources or engaged in a bitter ethnic war. With so many opposing factions, it has made reaching a solution difficult. While a rough peace treaty has been established, sporadic fighting pops up in the country everyday. The people of Congo areRead MoreRwand The Rwandan Genocide1296 Words   |  6 Pages The Rwandan genocide was the killing of 800,000 people in just 100 days. The Rwandan genocide took place in 1994. During this time Rwanda was a small country with a mostly agricultural economy. Although it is small it had one of the largest populations. In 1994 Rwanda was made up of three different ethnic groups. The Hutu made of 85% of the Rwandan population. The Tutsi’s made of 14% of the population and was the minority. The Tw a was a small Pygmy group that made up 1% of the population (unitedhumanrightsRead MoreThe Rwandan Genocide And The Genocide1393 Words   |  6 PagesThe Rwandan Genocide was one of the most violent genocides in the history of the world and was intricately planned and implemented by the ethnic group called the Hutu in an attempt to eliminate another, the Tutsis. Though the genocide lasted only one hundred days, the number of deaths is estimated to be approximately 800,000. In the wake of the genocide, mass chaos plagued the country of Rwanda, deepening the divide between the groups Hutu and Tutsi. Although it can be said the genocide was causedRead MoreAn Inside Look at Rwanda Essays1195 Words   |  5 PagesRwanda is one of the smaller countries in Africa located south of the equator in Central/ Eastern Africa. It has a number of lakes, the largest being Lake Kivu. Mountains cut through the majority of Central and Western Rwanda, its Eastern border, however consists of swamps, savannas and plains. Rwanda is bordered by Uganda, Tanzania, Burundi, and the Democratic Republic of Congo. The country is home to various cultures and languages such as Kinyarwanda (Bantu) and French. Although mostly recoveredRead MoreA Look at the Rwandan Genocide Essay1014 Words   |  5 Pagesterrible economies. People are suffering and have very little hope. Genocide is the only reason. Everything could have been prevented if genocide didn’t exist. The world basically ignored the genocide and pretended like it never happened because they didn’t want to spend the money. Thousands of people could still be alive if the world stepped up at helped the victims of this horrible crime. Rwanda used to be a peaceful country until the Civil war started. Belgium then took over Rwanda and put theRead MoreRwanda During The Colonial Era1502 Words   |  7 Pagescolonial era, Rwanda had larger population of Hutus compared to Tutsis and Twa. Rwanda as a country was divided into three ethnic groups i.e. Hutu (approximately about 85%), Tutsi (14%) and Twa (1%) (United Nations). Although, Tutsis were the minorities, they belonged to the higher strata compared to the other ethnic groups; Tutsis were privileged and had power and control over the Hutus and Twas. â€Å"Hutus were formerly bound to their Tutsi patrons via client ship† (Sinema, 2012). When Rwanda was colonized

The Exxon Valdez 1989 Oil Spill Free Essays

This summary will briefly discuss three topics: a) the oil spill, b) the environmental damage and clean up, and c) the insurance coverage settlements. This paper will then focus on the insurance coverage settlements. Afterwards, it will provide an analysis on the effectiveness of the dispute resolution process. We will write a custom essay sample on The Exxon Valdez 1989 Oil Spill or any similar topic only for you Order Now The Exxon Valdez Oil Spill of 1989 was one of the largest manmade environmental disasters (Rodgers et al, 2005, p. 136). It occurred in U. S. waters at Prince William Sound, Alaska in March 1989 (Rodgers et al, 2005, p. 136). The oil tanker, Exxon Valdez, struck a reef and discharged an estimated 10. 8 million gallons of oil according to Exxon estimates but other sources indicate that it is around 30 million gallons (Rodgers et al, 2005, p. 136). The oil belonged to Exxon Corporation while the tanker belonged to Exxon Shipping, its subsidiary (Holman, Fenwick Willan, 2004, p. 1). The environmental damage caused by the oil spill and the subsequent clean up of the spill and its contaminants became the subject of numerous litigations (Rodgers et al, 2005). Environmental damage claims and settlements ran into several billion U. S. dollars (Rodgers et al, 2005, p. 149-88). Oil spill clean up expenses likewise ran into several billion U. S. dollars (Holman, Fenwick Willan, 2004, p. 2). In this regard, due to the huge volume of lawsuits, the complexity of the case or cases, the wide coverage of the disaster, and the disaster’s far-reaching implications among other considerations, Exxon Corporation undertook a wide variety of legal strategies. One of those strategies involved alternative dispute resolution through settlements for insurance coverage disputes. The Exxon insurance coverage disputes are complex (Covington Burling LLP, 2007). One point of consideration is that Exxon’s primary insurers are reinsured with Lloyd’s London (Holman, Fenwick Willan, 2004, p. 2). This complicates the disputes since Exxon is an American company while its underwriters are international business entities. Hence, the dispute involved significant activities in many locations: Texas, New York, London, Oslo, Alaska and other places (Covington Burling LLP, 2007). As such, issues on jurisdiction and applicability of laws whether English law or New York law should be applied made litigations costly and long. Covington Burling LLP represented Exxon from 1991 to 1997 in â€Å"its hotly contested, multi-forum claims for coverage of losses arising out of the grounding of the Valdez† (Covington Burling LLP, 2007). In early 1997, these disputes ended after Exxon and the Lloyd’s consortium of international underwriters and various Scandinavian companies settled for $780 million (Treaster, 1996; Covington Burling LLP, 2007). Covington Burling LLP (2007) best describes the legal complexity of these disputes, to quote: The Exxon claims arose out of the company’s Global Corporate Excess package of policies for 1988-89, which was characterized by high limits and high retentions. Exxon claimed coverage under various sections of the package, including the first-party property section’s cover for removal of debris, the marine liability section’s cover for cargo-owner pollution losses, and the general liability section’s cover for pollution clean-up costs. Meanwhile, the Covington Burling LLP strategy involved: a) â€Å"a non-binding ADR procedure moderated by a London-based barrister before any litigation commenced;† b) â€Å"a Texas lawsuit filed by Exxon that the underwriters unsuccessfully sought three times to remove and that resulted in a jury verdict for Exxon on one of its three claims;† c) â€Å"an arbitration proceeding in New York;† d) â€Å"a federal declaratory judgment action in New York that the underwriters struggled to keep alive despite a dismissal and multiple trips to the Second Circuit and the Supreme Court on jurisdictional issues;† and finally, e) â€Å"two settlements — one for $300 million before the Texas verdict and one for $480 million while the Texas verdict was on appeal and just before the arbitration hearing was to commence† (2007). Many forms of alternative dispute resolutions or ADR can be made. Balmer (n. d. ) notes that several types of ADR can in fact be customized as can be seen from the Exxon insurance settlements. Some of these customized ADRs can range â€Å"from non-assisted discussions through mediation, neutral fact finders, case exposure such as mini-trials, arbitration both binding and non-binding, and limited issue litigation† (Balmer). Exxon already spent some U. S. $ 2. 5 Billion in damage claims as a result of the oil spill (Rodgers et al, 2005). Without ADR, it would have been unable to recover some $780 million from its insurance coverage (Treaster, 1996) while Exxon’s insurance disputes could have been unnecessarily protracted. For this incident, Exxon employed litigation but was always open to the many forms of alternative dispute resolution. For instance, Exxon used mediation through a non-binding ADR procedure moderated by a London-based barrister before any litigation commenced (Covington Burling LLP, 2007). Technically, mediation involves a neutral third party who helps in hammering out a resolution (Balmer). In another instance, Exxon employed arbitration proceedings. Balmer describes arbitration as â€Å"getting a neutral party or panel to reach a decision on facts, law or both.† Most importantly, Exxon often used settlements. How to cite The Exxon Valdez 1989 Oil Spill, Papers

Analysis of Linear DNA Genomes Separation in Gel Electrophoresis

Question: Discuss about theAnalysis of Linear DNA Genomes Separation in Gel Electrophoresis. Answer: Introduction Agarose gel electrophoresis has been widely used as a form of separating DNA genomes in varying sizes from 100 kp upto 25 kb. Isolation of Agarose gel is obtained from the genera Gelidium and Gracilaria.in the gelato process, the polymers of agarose often form an association of none covalent which form networks of pore sizes which determine the molecular ability of sieving properties. Use of gel electrophoresis is beneficial in separation of DNA genomes. Electrophoresis process is key in separating the different nucleic acids using various sizes and charges depending on the contents of the solution. In this experiment, lab analysis of gel was used to put gel solutions in charged nucleic acids for separation purposes. At this point the larger DNA and RNA have a hard time in separating thus allowing time for separation of the genomes based on the sizes. The rate of separation of the DNA molecule in the experiment was determined by the rate at which the sizes of the DNA, the concentration of the gel, DNA Conformation present, voltage degree applied, ehidium bromide solution introduced, type of agarose and the buffer being utilized in electrophoresis. After the process of separation, DNA molecules will be able to be visualized in the UV light using staining process to identify the different genomes. Thus in essence DAN electrophoresis defines the process by which the DNA migrates in the supporting medium. Most of electrophoresis is carried in agarose gels in narrow polymers of gels using pores of different sizes, this sieving provides a means by which the pores gives an opportunity for the DNA molecules to go through the pores at different sizes thus being separated using molecular weights. Thus this laboratory report uses agarose Gels while staining with ethidium bromide to assess the separation process of the different DNA genomes. Thus it seeks to investigate the DNA genome separation to assess the different nucleic acids by their respective sizes. Materials and methods Refer to the Lab Manual 5 for in-depth methodology and procedure. Results Diagrammatic presentation of gel DNA Table 1; Showing gel electrophoresis picture Standard curve for DNA ladder Table 2; Showing curve presentation of the base pairs against distance travelled Table of standard curve values Bp size 100 200 300 400 Log10(bp) 2 2.3 2.3 2.4 Distance cm 0.5 0.4 0.4 0.38 Table 3; Showing table figure for the curve Calculation process Table 4; Showing how to calculate base pairs Example suppose we have a base pair having travelled 0.3 cm, then draw a line as illustrated above and take the readings on the corresponding logbp and take the anti log, which you get the base pair size. This gives us anti log of 3.0, which is 1000kbp Insert values table Bp size 100 200 300 400 Log10(bp) 2 2.3 2.3 2.4 Distance 0.5 0.4 0.4 0.38 Size of pUC19 100,200,300, 400, 500,600 700,800,900, 1000,1500 2000,2500, 3000,4000, 5000,6000 8000,10000 Size of insert 0.1kbp 0.2kbp 0.3kbp 0.4kbp Table 5; Showing the sizes of pUC19 and their insert sizes Discussion Agarose gel electrophoresis has been utilised as a common method for separation of proteins, (Kryndushkin et al., 2003). The basic forms of nucleic acids can be separated through the aid of electrification process whereby charged molecules move to the anode side. This migration as depicted in the experiment ensures that molecules which have lower molecular weight are able to move faster, (Sambrook Russel 2001). The process of electrophoresis is a crucial step in ensuring purification process of the desired DNA bands. In this experiment the usage of ethidium bromide is essential in visualizing the staining of the transcend DNA molecules. In this task, the Agarose gel electrophoresis plays a key role in ensuring the characteristics of DNA are obtained without any alterations. This experiment has yielded results which have enabled determination of DNA fragments sizes through digestion by restriction enzymes. The visualization has been effected with the use of ethidium bromide which is a common agent in nucleic acid purification process. The Agarose gel concentration on this task entailed the separation of the gel using agarose gel concentration of 0.2%w/v having bands from 0.1-1 kb. The distance travelled by DNA molecules in electrophoresis is directly proportional to the size of the DNA itself. The agarose gel is beneficial in ensuring that there are movements based on their sizes. With the various differences between the various rates of the DNA molecules in the gel solution, they are separated based on the size of the bases. The relationship built between the varied sizes of the DNA genome. The sieving of DNA is done through the size which it bears, (Southern, 1975). The length of DNA strands often vary from 50 base pairs to upto million s base pairs which agarose gel electrophoresis can be effective in separating them , the migration and distance travelled is linked on the concentration of the agarose used to prepare the gel. Concentrations having lower concentration are able to travel faster in the distance travelled and vice versa. In this study agarose gel of 2% has been used which was effective in separating the DNA at range of 0.1-1 kb, the low percentile gels often signify gels which are weak. Double stranded DNA moves faster as the molecules travels; its speed is inversely proportional to the logarithm of base pairs. This linked and established relationships depends on the strength of the of gel composition. The distance travelled by the digested genome signifies that there is action of restriction enzymes which shows that there restrictions which have taken place, thus distinguishing the variability linked to genetics and enzyme cost. The digested fragments were this separated using the agarose gel electrophoresis which showed continuous smear on the gel surface with the distribution of the difference fragment sizes being established. Digested pUC19 is a plasmid and able to transform itself on the transformation process where it can be able to multiply itself and express. Undigested pUC19 originate from E coli and contain high number of base pairs. The transformation efficiently portrayed shows that smaller pUC19 plasmid sin E choli can be manipulated and be transformed from the ampicilin forms. This shows that the DNA is in contact form with plasmid DNA being intact and with presence of viral chromosomes which can be transformed into high efficiencies. This transformation is through the resulting effect of digestion of peri plasmids. The undigested Puc19 shows presence base pairs which have the ability to perform recombination and be incorporated into cells, (Goto, Kenta Yukio, 2013). The lanes which have recombination factor is able to facilitate the cloning of DNA in host cells. This signifies recombination of various fragments of gel solution. The lanes that have been generated originated from digestion of particular DNA, which gives it equimolar amounts. Based on the lanes, there is variation on the number of non molar amounts, thus signifying that there is difference in band lengths. Others have shown to represent circular forms of the plasmids which is dependent on the age and quality of the plasmids. The existence of three forms of DNA formation which exists include linear formation, open circular formation and supercoiled forms. Plasmid DNA have been prevalently been studied in laboratory studies. After its preparation they exists in the three forms above. With good plasmid preparation, DNA often form plasmid which exist in any one strands of the DNA, this break causes the release of the phosphordiester backbones of the DNA to be released out. The visualising process of the agarose gel using the standard control tool is key to assess whether the bands have created a generation or not. Closer bands are well compressed than far away bands as indicated in the gel view. The standard marker used in this experiment was essential in ensuring that the standards sizes are generated using base pairs. This result signifies that electrophoresis is an effective way of separating nucleic acids. High gel agarose gives room for handling of low percentage gel separation. Due to the size of the base pair present in this experiment, has utilised field gel electrophoresis. This is comparable to studies done (Lee et al, 2012), which have shown that sizes of DNA can be separated effectively through plotting on the log of molecular weight and different bands of DNA against the distance moved, this portray how different forms of gel can be able to move at different speeds. Super coiled plasmid DNA have sown to move faster, while those in linear formation travel averagely while open circular travel slowly. References Goto, K., Nagano, Y. (2013). Ultra-low background DNA cloning system. PloS one, 8(2), e56530. Kryndushkin DS, Alexandrov IM, Ter-Avanesyan MD Kushnirov VV (2003). Yeast [PSI+] prion aggregates are formed by small Sup35 polymers fragmented by Hsp10. Journal of Biological Chemistry.278 (49): 49636. Lee, P. Y., Costumbrado, J., Hsu, C. Y., Kim, Y. H. (2012). Agarose gel electrophoresis for the separation of DNA fragments. Journal of visualized experiments: JoVE, (62). Sambrook JRussel DW(2001). Molecular Cloning: A Laboratory Manual 3rd Ed. Cold Spring Harbor Laboratory Press. Cold Spring Harbor, NY. Southern, E. M. (1975). Detection of specific sequences among DNA fragments separated by gel electrophoresis. J mol biol, 98(3), 503-517.