Wiktor Igorewitsch Budjanski

Wiktor Igorewitsch Budjanski (russisch Виктор Игоревич Будянский; * 12. Januar 1984 in Wowtschansk, Ukrainische SSR) ist ein russischer Fußballspieler, der aktuell vereinslos ist.

Budjanski wechselte zur Saison 2003/04 zum italienischen Rekordmeister Juventus Turin, jedoch vermochte er sich gegen die große Konkurrenz nicht durchzusetzen und kam nur zu zwei Einsätzen. Zur Saison 2004/05 ging der gebürtige Ukrainer dann zum Ligakonkurrenten Reggina Calcio

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, jedoch lief es hier auch nicht besser als bei der „Alten Dame“. Deshalb unterschrieb er am Ende der Saison beim Serie B-Verein US Avellino; hier wurde Budjanski regelmäßig eingesetzt und konnte sein erstes Tor in Italien erzielen. Zur Saison 2006/07 wechselte er zu Ascoli Calcio und kehrte somit in die Serie A zurück. Doch nur ein Jahr später wechselte er zu Udinese Calcio. Dort absolvierte er bisher ein Spiel. Danach folgten zwei Leihfristen bei US Lecce und FK Chimki.

Nach guten Leistungen bei Ascoli Calcio debütierte Wiktor Budjanski am 2. Juni 2007 im Spiel gegen Andorra in der russischen Nationalmannschaft.

Inschrift von Parahyba

Die Inschrift von Parahyba (oder Tafel von Paraíba) ist eine umstrittene Tafel mit phönizischen Inschriften, die angeblich in Brasilien entdeckt wurde. Sie soll einen Beweis für die Annahme transatlantischer Reisen der Phönizier nach Amerika liefern (vgl. Hypothetische Entdeckungsfahrten nach Amerika).

1873 wurde in Parahyba (angeblich von einem Sklaven) eine Tafel bzw. ein Stein entdeckt. Der genaue Fundort soll Pouso Alto in der Nähe des Paraíba-Flusses gewesen sein, in einem Besitztum des Joaquim Alves da Costa.

Ein Jahr später veröffentlichte der Direktor des brasilianischen Nationalmuseums eine Abschrift. Das Original ging verloren. Die Tafel löste jahrzehntelange Diskussionen aus. Letztlich setzte sich in Fachkreisen die Fälschungs-These durch. Zur damaligen Zeit wurden nämlich viele angeblich phönizische Artefakte, z. B. Münzen, in Südamerika entdeckt, die sich später als Fälschungen herausstellten (sog. Moabitica). Außerdem widersprach dieser Fund der – gegen Ende des 19. und während der 1. Hälfte des 20. Jahrhunderts in der Altamerikanistik vehement vertretenen – Lehrmeinung, zwischen ‘Alter’ und ‘Neuer Welt’ habe es keinerlei präkolumbische Kontakte gegeben. 1968 untersuchte der amerikanische Orientalist Cyrus H. Gordon erneut die Abschrift und hielt sie, aufgrund neuerer Erkenntnisse über die phönizische Sprache, für echt. Van den Branden, ein Kollege Gordons, datiert den Inhalt der Tafel aufgrund des verwendeten phönizisch-hebräischen Dialektes auf etwa 800 v. Chr. Gordon dagegen datiert den Text auf ca. 500 v. Chr. (er erkennt darin einen phönizisch-aramäischen Dialekt). Der Wiener Afrikanist und Berberologe Gerhard Böhm hält einige Fragmente der Inschrift für iberischen Ursprungs, die Gesamtinschrift aber für eine Fälschung des 19. Jahrhunderts. Nach F.M. Cross (1968) ist die Inschrift „ein erbärmlicher Mischmasch linguistischer Formen, Schreibweisen und Schriften verschiedenen Datums und Ortes, zusammengeschustert aus Handbüchern aus dem 19. Jahrhundert […] eine blanke Fälschung.“ (a pathetic mishmash of linguistic forms, of spellings, and of scripts of various dates and places patched together from nineteenth-century handbooks […] a plain fraud.) Der Bonner Theologe und Aramaistiker Lienhard Delekat sprach sich dagegen im folgenden Jahr für die Echtheit der Inschrift aus. Eine definitive und endgültige Klärung der Frage nach der Authentizität des Original-Fundstücks ist aufgrund seines Verschwindens jedenfalls nicht mehr möglich.

Deutsche Übersetzung:

Wir Söhne Kanaans sind aus der Stadt Sidon, Schiffsvolk und Händler, wurden geworfen an dieses ferne Ufer, ein Land der Berge. Wir opferten einen Jüngling für die erzürnten Götter und Göttinnen. Im neunzehnten Jahr des Hiram, unseres mächtigen Königs, des Führers, da gingen wir von Ezjon-Geber aus auf das Schilfmeer, und wir brachen auf mit zehn Schiffen, und wir waren auf dem Roten Meer miteinander. Zwei Jahre umfuhren wir das heiße Land, das Ham gehört, dann wurden wir getrennt von Jerub-Baal und wir betrauerten unsere Gefährten und wir kamen hierher, zwölf Männer und drei Frauen

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, auf eine Insel des Waldes, welche ich, Methu-Astart, der Führer, weihte als Eigentum der Götter und Göttinnen. Sie seien uns gnädig.

Mina ja Murri

Mina ja Murri (russisch Я и Мурри

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; zu deutsch „Ich und Murri“) ist der Titel eines estnischen Puppentrickfilms in Farbe aus dem Jahr 1961.

Das Hündchen Murri ist der treuste Freund des kleinen Filmhelden. Der Junge hat den großen Traum, einen riesigen Fisch zu fangen. Aber am Ufer des Sees stellt sich heraus, dass er noch nie geangelt hat. Die beiden Freunde müssen daher bei ihren Bemühungen zahlreiche Rückschläge einstecken

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… Mit gesenktem Kopf kehrt der gescheiterte Fischer nach Hause zurück.

Regisseur des Trickfilms für Schulkinder war Elbert Tuganov (1920–2007). Mina ja Murri war Tuganovs fünfter Film. Mit dem vorherigen Puppentrickfilm Ott kosmoses („Ott im Kosmos“) hatte Tuganov seinen Durchbruch als Filmemacher sowohl innerhalb der Sowjetunion als auch international geschafft.

Mit Mina ja Murri wurde endgültig die Puppentrickfilm-Produktion als feste Tradition bei Tallinnfilm etabliert.

History of chemical engineering

Chemical engineering as a discipline that was developed out of those practising “industrial chemistry” in the late 19th century. Before the Industrial Revolution (18th century), industrial chemicals and other consumer products such as soap were mainly produced through batch processing. Batch processing is labour-intensive and individuals mix predetermined amounts of ingredients in a vessel, heat, cool or pressurize the mixture for a predetermined length of time

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. The product may then be isolated, purified and tested to achieve a saleable product. Batch processes are still performed today on higher value products, such as pharmaceutical intermediates, speciality and formulated products such as perfumes and paints, or in food manufacture such as pure maple syrups, where a profit can still be made despite batch methods being slower and inefficient in terms of labour and equipment usage. Due to the application of Chemical Engineering techniques during manufacturing process development, larger volume chemicals are now produced through a continuous “assembly line” chemical processes. The Industrial Revolution was when a shift from batch to more continuous processing began to occur. Today commodity chemicals and petrochemicals are predominantly made using continuous manufacturing processes whereas speciality chemicals, fine chemicals and pharmaceuticals are made using batch processes.

The Industrial Revolution led to an unprecedented escalation in demand, both with regard to quantity and quality, for bulk chemicals such as soda ash. This meant two things: one, the size of the activity and the efficiency of operation had to be enlarged, and two, serious alternatives to batch processing, such as continuous operation, had to be examined.
Industrial Chemistry was being practised in the mid 1800s, but it was not until the 1880s that the engineering elements required to control chemical processes were being recognized as a distinct professional activity. Chemical engineering was first established as a profession in the United Kingdom when the first chemical engineering course was given at the University of Manchester in 1887 by George E. Davis in the form of twelve lectures covering various aspects of industrial chemical practice. As a consequence George E. Davis is regarded as the world’s first chemical engineer. Today, chemical engineering is a highly regarded profession. Chemical engineers with experience can become licensed Professional Engineers in the United States, aided by the National Society of Professional Engineers, or gain “Chartered” chemical-engineer status through the UK-based Institution of Chemical Engineers.
In 1880, the first attempt was made to form a Society of Chemical Engineers in London. This eventually resulted in the formation of the Society of Chemical Industry in 1881. The American Institute of Chemical Engineers (AIChE) was founded in 1908, and the UK Institution of Chemical Engineers (IChemE) in 1922. These both now have substantial international membership. Some other countries now have chemical engineering societies or sections within chemical or engineering societies, but the AIChE and IChemE remain the major ones in numbers and international spread: they are both open to suitably qualified professionals or students of chemical engineering anywhere in the world.
For the other established branches of engineering, there were ready associations in the mind of the common man: Mechanical Engineering meant machines, Electrical Engineering meant circuitry, and Civil Engineering meant structures. So chemical engineering can be symbolised as chemicals production.
The answer, provided by Arthur D. Little to the President of MIT, was to emphasize the approach chemical engineers took to the design and analysis of processes rather than a process or a product. The concept of Unit operations was developed to emphasize the underlying unity among seemingly different operations. For example, the principles are the same whether one is concerned about separating alcohol from water in a fermenter, or separating gasoline from diesel in a refinery, as long as the basis of separation is generation of a vapor of a different composition from the liquid. Therefore such separation processes can be studied together as a unit operation (in this case called distillation). The concept has stood the profession in good stead in its phase of growth, and has even been used to understand the way the human body functions

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In the early part of the last century, a parallel concept called Unit Processes was used to classify reactive processes. Thus oxidations, reductions, alkylations, etc

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. formed separate unit processes and were studied as such. This was natural considering the close affinity of chemical engineering to industrial chemistry at its inception. Gradually however, the subject of chemical reaction engineering has largely replaced the unit process concept. This subject looks at the entire body of chemical reactions as having a personality of its own, independent of the particular chemical species or chemical bonds involved. The latter does contribute to this personality in no small measure, but to design and operate chemical reactors, a knowledge of characteristics such as rate behaviour, thermodynamics, single or multiphase nature, etc. are more important. The emergence of chemical reaction engineering as a discipline truly signaled the severance of the umbilical cord connecting chemical engineering to industrial chemistry, and served to cement the truly unique character of this discipline.
Chemical Engineers are today focusing their disciplines on the use of alternative feedstocks such as biomass and societal waste to produce chemicals and energy. Their aim is to use less carbon in the manufacturing processes by making them more carbon efficient and these lower carbon processes is sometimes termed “Green Chemistry” or sustainable processing. An example of this is the work of the Northeast of England Bioresources Group (NEBR) created by the members of the Northeast of England Process Industry Cluster (NEPIC). Their work is aimed at creating the future biorefinery and other opportunities for energy and products to be manufactured from biomass and waste materials. An example where such work has brought results is with Coca Cola who have already required the commodity chemical polyethylene terephthalate (PET) to be produced in a more environmentally friendly way for use in their soft drinks bottles and their product “PlantBottle” was introduced in 2009.
In the 21st century most professional Chemical Engineers work in contract engineering companies or in the process industry companies that such engineering contractors serve. These are Commodity-speciality-fine chemical, petrochemical, pharmaceutical, biotechnology, polymer and renewable energy and sustainable materials companies. Many such companies can be found clustered around the large scale infrastructure that these industries need, such as ports, power stations, storage facilities, pipelines etc. This infrastructure is particularly important to commodity and petrochemical companies. An example of such a location is on Teesside in the Northeast of the United Kingdom where the process industry companies and the engineering companies collaborate through membership of the Northeast of England Process Industry Cluster (NEPIC). In this region

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, as well as the process industry companies themselves, there is a particularly high number of engineering suppliers supporting the sector. This includes offices of global suppliers like ABB, Jacobs, AMEC and Foster Wheeler as well as many local firms that also serve the industry internationally,such as KHome International, Cordell, Hertel etc. Chemical Engineers also contribute to industry via specialist technology companies again examples in the NEPIC Cluster are companies such as DRD Power, and CompactGTL. One report has suggested that the highest concentration of such knowledge intensive businesses (KIBS) in Europe can be found in Northeast England and a significant number of their 14000 employees are chemical engineers. In locations such as this Chemical Engineers share best practice through local sub-groups of their Professional Institution. The Teesside sub-group of the Institution of Chemical Engineers regularly meet to present updates on technical and operational issues and to share best practice. Furthermore Chemical Engineering degree courses and research takes place at the local universities such as Teesside University and Newcastle University

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.

James Findlay (Politiker, 1770)

James Findlay (* 12. Oktober 1770 in Mercersburg, Franklin County, Pennsylvania; † 28. Dezember 1835 in Cincinnati, Ohio) war ein US-amerikanischer Politiker der Demokratischen Partei. In den Jahren von 1805 bis 1806 und 1810 bis 1811 war er Bürgermeister von Cincinnati. Von 1825 bis 1833 war er Mitglied des Repräsentantenhauses der Vereinigten Staaten für den 1. Kongressdistrikt des Bundesstaates Ohio.
James Findlay wurde in Mercersburg als Sohn von Samuel Findlay und Jane Smith geboren. Er hatte zwei Brüder, William Findlay

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, der später Gouverneur von Pennsylvania wurde, und John Findlay, der später Pennsylvania im Repräsentantenhaus vertrat

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. Nachdem sein Vater finanzielle Rückschläge hinnehmen musste, zog er mit seiner Frau Jane Irwin 1793 nach Cincinnati in das damalige Nordwestterritorium. Gemeinsam mit dem späteren Senator John Smith wurde er schon recht bald ein einflussreicher Geschäftsmann. Von 1799 bis 1802 war er erster Vertreter des Hamilton County im Repräsentantenhaus des Nordwestterritoriums. 1802 wurde er United States Marshal für den Ohio Country. 1805 wurde er zum ersten Mal Bürgermeister von Cincinnati. Diese Amtszeit dauerte bis 1806. Von 1810 bis 1811 war er erneut Bürgermeister. Im Britisch-Amerikanischen Krieg 1812 diente er in der US Army als Colonel.
1825 wurde er als Demokrat ins US-Repräsentantenhaus gewählt. Seine Amtszeit dauerte bis 1833, nachdem Robert Todd Lytle ihn besiegen konnte. 1834 kandidierte er erfolglos für den Gouverneursposten, Robert Lucas, der Amtsinhaber, konnte sich erwartungsgemäß durchsetzen.
Findlay starb 1835 und wurde auf dem Spring Grove Cemetery beigesetzt.
Delegierte aus dem Nordwestterritorium (1799–1803) W. Harrison | McMillan | Fearing
Abgeordnete aus dem Bundesstaat Ohio (seit 1803) 1. Bezirk: Morrow | J. McLean | W. Harrison | Ross | Gazlay | Findlay | Lytle | Storer Sr. | Duncan | N. Pendleton | Duncan | Faran | Disney | Day | G. Pendleton | Eggleston | Strader | Perry | Dodds | Sayler | Butterworth | Follett | Butterworth | Storer Jr. | C. Taft | Shattuc | Longworth | Bowdle | Longworth | Hollister | Dixon | Elston | Scherer | Rich | Gilligan | R. Taft | Keating | T. Luken | Gradison | T. Luken | C. Luken | Mann | Chabot | Driehaus | Chabot • 2. Bezirk: Alexander | J. W. Campbell | Ross | Woods | Shields | T. Corwin | Webster | Weller | Cunningham | Fisher | L. Campbell | J. Harrison | Groesbeck | Gurley | Long | Hayes | Cary | Stevenson | Banning | Young | Jordan | Brown | Caldwell | Bromwell | Goebel | A. Allen | Heintz | Stephens | Tatgenhorst | Hess | Bigelow | Hess | Wagner | Hess | Clancy | T. Luken | Gradison | Portman | Schmidt | Wenstrup • 3. Bezirk: Creighton | Barber | Brush | Barber | W. McLean | Crane | Goode | R. Schenck | Bell | L. Campbell | Vallandigham | R. Schenck | L. Campbell | Smith | Savage | M. Gardner | McMahon | Morey | Murray | J. E. Campbell | E. Williams | Houk | Sorg | Brenner | Nevin | Harding | Cox | Gard | R

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. Fitzgerald | Harlan | Routzohn | Holbrock | Jeffrey | E. Gardner | Burke | Breen | P. Schenck | Love | Whalen | Hall | Turner | Beatty • 4. Bezirk: Caldwell | Herrick | Chambers | Vance | T. Corwin | Vance | Canby | M. Corwin | Stanton | Nichols | W. Allen | McKinney | Lawrence | McKinney | Gunckel | McMahon | Keifer | Shultz | Le Fevre | Anderson | Yoder | Gantz | Layton | G. Marshall | R. Gordon | Garber | Tou Velle | Goeke | J. Russell | Welty | Cable | W. Fitzgerald | Cable | Kloeb | Albaugh | R. Jones | McCulloch | Guyer | Oxley | Jordan 
5. Bezirk: Kilbourne | Beecher | Vance | J. W. Campbell | W. Russell | Hamer | Doan | Potter | Sawyer | Potter | Edgerton | Mott | Ashley | Le Blond | Mungen | Lamison | Rice | Le Fevre | Seney | Le Fevre | Seney | Layton | Donovan | De Witt | Meekison | Snook | W. Campbell | Ansberry | Matthews | Snook | Thompson | Kniffin | Clevenger | D. Latta | Gillmor | B. Latta • 6. Bezirk: Beall | Clendenin | Hitchcock | Sloane | McArthur | Thomson | Creighton | Muhlenberg | Creighton | Vinton | Morris | John | Dickinson | Wood | Bell | Green | Ellison | Emrie | Cockerill | Howard | C. White | Clarke | Smith | Sherwood | Hurd | J. Cox | Hill | Ritchie | Hill | Boothman | Donovan | Hulick | Brown | Hildebrant | Scroggy | Denver | Fess | Kearns | Polk | Davis | McCowen | Polk | Miller | Harsha | McEwen | Strickland | Cremeans | Strickland | C. Wilson | B. Johnson • 7. Bezirk: Vinton | Allen I | Bond | W. Russell | McDowell | Morris | Barrere | Harlan | T. Corwin | R. Harrison | S. Cox | Shellabarger | Winans | Shellabarger | Neal | Dickey | Hurd | Leedom | Morey | J. E. Campbell | Seney | J. E. Campbell | Morey | Haynes | G. Wilson | Weaver | Kyle | Keifer | Post | Fess | Brand | L. T. Marshall | Aleshire | C. Brown | B. Brown | DeWine | Hobson | Austria | Gibbs • 8. Bezirk: W. Wilson | Stanbery | McLene | Ridgway | Vanmeter | Thurman | J. Taylor | M. Corwin | Stanton | Shellabarger | Johnston | Hubbell | C. Hamilton | Beatty | Lawrence II | Keifer | Finley | Keifer | Little | Kennedy | Hare | Strong | Lybrand | Warnock | R. D. Cole | Willis | Key | R. C. Cole | Fletcher | Mouser Jr. | Fletcher | F. Smith | Betts | Powell | Kindness | Lukens | Boehner 
9. Bezirk: Beecher | Irvin | Chaney | Medill | Florence | Perrill | Edwards | Olds | Green | Watson | L. Hall | J. Carey | Noble | Buckland | Dickinson | C. Foster | J. W. Robinson | Poppleton | Jones | Converse | J. S. Robinson | Cooper | Outhwaite | Ritchie | Southard | Sherwood | Chalmers | Sherwood | Chalmers | W. White | Duffey | Hunter | Ramey | Burke | Reams | Ashley | Weber | Kaptur • 10. Bezirk: Patterson | Jennings | Shannon | Davenport | Kennon | Vance | Mason | Moore | Stone | Delano | Duncan | Sweetser | Taylor | Moore | J. Miller | Trimble | Ashley | Hoag | Peck | C. Foster | Ewing Jr. | Rice | Hurd | Romeis | Haynes | Doan | Enochs | Bundy | Fenton | Morgan | Bannon | A. Johnson | Switzer | I. Foster | Jenkins | Moeller | Abele | Moeller | C. Miller | Hoke | Kucinich | Turner • 11. Bezirk: Wright | Goodenow | Leavitt | Bell | Kennon | Alexander Jr. | Parrish | Cowen | Brinkerhoff | J. K. Miller | Busby | Ritchey | Horton | Martin | Horton | W. Hutchins | Bundy | J. Wilson | Bundy | Vance | Neal | Dickey | Neal | McCormick | Ellsberry | A. Thompson | Pattison | Grosvenor | Douglas | H. C. Claypool | Ricketts | H. C. Claypool | Ricketts | Underwood | Hammond | H. K. Claypool | Brehm | O. Bolton | Dennison | Cook | O. Bolton | Stanton | Eckart | Stokes | S. Jones | Fudge • 12. Bezirk: Sloane | Thomson | Mitchell | Howell | Harper | Taylor | Mathiot | Vinton | Welch | Olds | Galloway | S. Cox | Finck | Van Trump | Jewett | Finck | Walling | Ewing Jr. | Neal | Converse | Hart | Thompson | Pugsley | Enochs | Outhwaite | Watson | Lentz | Tompkins | Badger | E. Taylor | Brumbaugh | Speaks | Lamneck | Vorys | Devine | Shamansky | Kasich | Tiberi 
13. Bezirk: E. Whittlesey | Spangler | Leadbetter | Mathews | P. Johnson | Parrish | Ritchey | W. Whittlesey | Gaylord | Lindsley | Sherman | Worcester | O’Neill | Delano | Morgan | Delano | Morgan | Southard | Warner | Atherton | Converse | Outhwaite | Dungan | Hare | Harris | Norton | A. Jackson | Mouser | Anderson | Key | Overmyer | Begg | Baird | Fiesinger | D. White | Baumhart | Weichel | Baumhart | Mosher | Pease | S. Brown | Sutton | Ryan • 14. Bezirk: Bartley | E. Cooke | W. Patterson | Hunter | Sweeny | Harper | Evans | Harper | H. Johnson | P. Bliss | Spink | Blake | G. Bliss | Welker | Monroe | Berry | Cowan | Finley | Atherton | Geddes | Grosvenor | Wickham | Owens | Harter | Kerr | Skiles | Webber | Laning | Sharp | S. Williams | Bathrick | Davey | Knight | Davey | F. Seiberling | D. Harter | Rowe | Huber | Ayres | J. Seiberling | Sawyer | LaTourette | Joyce • 15. Bezirk: J. Sloane | Allen | Andrews | Morris | Kennon Jr. | Hunter | Sapp | Burns | Helmick | Nugen | Morris | Plants | Moore | Sprague | Van Vorhes | Geddes | R. Dawes | Warner | Wilkins | Grosvenor | Harter | Van Voorhis | B. Dawes | Joyce | White | Mooney | White | Moore | Secrest | Griffiths | Secrest | Henderson | Moorehead | Secrest | Wylie | Pryce | Kilroy | Stivers • 16. Bezirk: E. Whittlesey | Giddings | Mathews | Cummins | Hoagland | J. Johnson | Ball | Tompkins | Cutler | J. White | Bingham | Danford | McKinley | Updegraff | J. Taylor | Wilkins | Geddes | Wilkins | Owens | Warwick | Ohliger | Pearson | Danford | Gill | Weems | Hollingsworth | Francis | McCulloch | Himes | McSweeney | McClintock | Thom | Seccombe | Thom | Carson | Thom | Carson | McSweeney | Bow | Regula | Boccieri | Renacci 
17. Bezirk: Thomson | Loomis | Coffin | Hastings | McCauslen | Fries | Cable | Shannon | Albright | Lawrence | Theaker | Morris | Eckley | Ambler | Woodworth | McKinley | Monroe | McKinley | J. Taylor | Warner | J. Taylor | Pearson | Richards | McClure | McDowell | Cassingham | Smyser | W. Ashbrook | Morgan | West | W. Ashbrook | McGregor | Levering | J. Ashbrook | J

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. S. Ashbrook | L. Williams | Traficant | Ryan • 18. Bezirk: B. Jones | Shepler | Starkweather | Dean | Starkweather | Lahm | Cartter | Bliss | Leiter | Edgerton | Spalding | Upson | Monroe | Updegraff | McClure | McKinley | Wallace | I. Taylor | McKinley | J. Taylor | Ikirt | Tayler | Kennedy | Whitacre | Hollingsworth | Murphy | Imhoff | Lewis | Imhoff | Lewis | Hays | Applegate | Ney | Space | Gibbs • 19. Bezirk: Leavitt | Kilgore | Swearingen | Stokely | Tilden | Crowell | Newton | Wade | Riddle | Garfield | E. Taylor | Northway | Dick | Thomas | Bathrick | Cooper | Kirwan | Carney | L. Williams | E. Feighan | Fingerhut | LaTourette • 20. Bezirk: Giddings | J. Hutchins | Parsons | Payne | Townsend | Paige | McKinley | Crouse | Smyser | V. Taylor | W. White | Beach | Phillips | Beidler | Howland | W. Gordon | Mooney | Norton | Mooney | M. Sweeney | M. Feighan | Stanton | Oakar
21. Bezirk: Brinkerhoff | Hamlin | Root | Townshend | Stuart | Bingham | Foran | Burton | Johnson | Burton | Cassidy | Bulkley | Crosser | Babka | Gahn | Crosser | Vanik | Stokes • 22. Bezirk: Crosser | Emerson | Burton | C. Bolton | Fleger | C. Bolton | F. Bolton | Vanik | Eckart • 23. Bezirk: Truax | Earhart | McSweeney | Bender | Young | Bender | Minshall | Mottl • 24. Bezirk: Young | Mosier | L. L. Marshall | Young | R. Taft | R. Sweeney | Lukens | Powell

John Holmes Jellett

John Holmes Jellett OBE, DSc, MA (1905–1971) was a British civil engineer.
Jellett was appointed assistant civil engineer to the Admiralty on 22 June 1933. He served in the Royal Navy Volunteer Reserve during the Second World War and was commissioned as a Temporary Captain. His engineering talents were called upon during the Invasion of Normandy where he was made Superintending Civil Engineer of Mulberry Harbour B, a temporary concrete harbour built at Arromanches

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. Mulberry B was in use for five months following the invasion and landed two million men, half a million vehicles and four million tons of supplies for the Liberation of Europe.
In recognition of Jellett’s work with the Mulberry harbour he was appointed an Officer of the Order of the British Empire (military division) on 28 November 1944. His citation in the London Gazette referred to his “distinguished service in operations which led to the successful landing of allied forces in Normandy”.
After the war from October 1945 to February 1946 he was Superintending Civil Engineer, HM Dockyard, Chatham. From 1946-48 he was Deputy Docks Engineer, Southern Railway, Southampton Docks. After nationalisation of the railway companies he was Docks Engineer, Southampton Docks, British Transport Commission from 1948–58 and he was Chief Docks Engineer, Southampton Docks from 1958 until his retirement in 1966

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.
He also acted as an occasional advisor within the Engineer and Railway Staff Corps, he was promoted to Major of that corps on 3 July 1957. In 1966 he was elected a first class engineer member of the Smeatonian Society of Civil Engineers. Jellett served as President of the Institution of Civil Engineers from November 1968 to November 1969

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. He authored the Harbours and Sea Works article entry in Encyclopaedia Britannica. He lived in Southampton in Hampshire, from 1946 until his death in 1971

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.

Jeon-gwan ye-u

Jeon-gwan ye-u refers to an informal arrangement in the South Korean legal system whereby retired judges and public prosecutors who go on to become lawyers in private practise receive special treatment from their incumbent former colleagues. A paper from the Korea Institute of Public Administration describes it as one of the four major problems caused by the way in which South Korea appoints judicial officers. The term may also be used more broadly to refer to preferential treatment for retired regulators who go on to take private-sector jobs in the industries which they were previously responsible for regulating, a form of regulatory capture.
It is variously translated into English as:

Jeon-gwan ye-u is said to be a result of South Korea’s system of legal education and appointment of judges. All law students who pass the bar examination (formerly limited to 300 students, though the cutoff was raised to 1,000 in the early 2000s) attend a two-year course at the Judicial Training Research Institute before being considered for appointment as a judge or public prosecutor; this training offers them the opportunity to develop close bonds with one another. Those who are not appointed have the option of becoming defense attorneys, or pursuing other professions. Judges and public prosecutors are thus appointed to their positions at a young age, and many retire early, in their 40s and 50s, in order to work as private attorneys.
The exact nature of the “special consideration” may vary. Prosecutors and judges, for their part deny that there is any impropriety at all

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. However, as stated by the Doosan Encyclopedia, the practise may extend as far as former judges and prosecutors being given a favourable ruling at their first trial in private practise, regardless of its merits. Because of the perception that it will offer them an advantage in their cases, clients thus prefer to engage the services of defense attorneys who have previously served as judges or public prosecutors. Judges-turned-lawyers are thus able to command much higher fees than their competitors. These factors have resulted in “deep-rooted distrust in the criminal justice system” by the public.
In 2003, a Supreme Court of South Korea spokesperson admitted that cases taken up by former Supreme Court officials had a far lower rate of dismissal than cases in general. In a 2006 article about the jeon-gwan ye-u phenomenon, South Korean newspaper Hankyoreh reported that of 32 former Supreme Court judges who had retired since 1990, 29 had since gone into private practise, indicating the potential extent of the phenomenon. The group of retired judges as a whole exhibited an unusually high acceptance rate for their cases of 63.2%, among whom the two highest were Yi Don-hoe at 94.3% and Song Jin-hun at 92.7%. A 2008 statistical analysis of the problem in the Hankook Ilbo, centred on seven former Supreme Court judges who retired in 2005 to take up private practise, found that from July 2006 to June 2008, only 26% of their 225 civil cases which went before the Supreme Court were dismissed, in comparison to an average rate of 58 to 63% for all lawyers. Below the Supreme Court, the ratio of former District Court officials who took on district court criminal cases from 2004 to 2006 (as a proportion of all lawyers appearing before the district court) ranged from a high of 100% (18 out of 18) in Suwon, to a low of 32% (9 out of 28) in Cheongju; eight out of the nine top-ranking districts in this regard were in the Seoul National Capital Area.
Efforts were made as early as 1973 to control the issue of jeon-gwan ye-u, by placing limits on the ability of retired prosecutors and judges to open their own law firms. Later, a new law was proposed in 1998, specifying that a lawyer who was once a judge or a prosecutor must not serve as a lawyer within two years at criminal trials of a court of which he was a member directly before. The law did not pass the National Assembly due to pressure from the assembly’s own Legal Affairs Committee as well as the legal profession at large; however

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, it was again proposed in 1999, and passed in January 2000. In December 2004, the Judicial Reform Commission proposed the creation of a voluntary central judicial ethics council as a means of controlling the problem. In March 2010, the Grand National Party proposed widening the restrictions, barring judges-turned-lawyers from taking cases in the entire region where they previously served as district judges for a period of one year

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.

Assertion

En linguistique et en philosophie, une assertion représente un énoncé considéré ou présenté comme vrai.
En logique et en mathématiques

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, une assertion est une proposition mathématique vraie. Cette proposition vraie s’inscrit dans le cadre d’une théorie précisée. Cette même proposition peut d’ailleurs être fausse au sein d’une autre théorie (voir exemples ci-dessous).
En programmation informatique, une assertion est une expression qui doit être évaluée à vrai

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. Si cette évaluation échoue elle peut mettre fin à l’exécution du programme, ou bien lancer une exception. Par exemple, la fonction assert de la bibliothèque standard du langage C termine l’exécution du programme si l’assertion est fausse. La programmation par contrat et les tests unitaires sont basés sur les assertions

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Nous entendons souvent dire que 2 + 2 = 5 est une affirmation fausse ; en fait cela sous-entend que 2 et 5 sont des entiers et en utilisant la propriété additive sur l’ensemble des entiers , nous aboutissons à une contradiction évidente 1 = 0

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, par exemple. Mais nous pouvons faire devenir vraie cette égalité en considérant 2 et 5 comme égaux à 0 et en définissant l’addition par 0 + 0 = 0. Nous construisons dans ce cas une autre théorie ; tout le problème est de savoir si ensuite cette théorie sera d’une quelconque utilité. Et pourra-t-on trouver beaucoup d’adeptes de cette théorie ? Après tout, des savants italiens du XVIe siècle comme Cardan s’enhardissaient à travailler avec des racines carrées de nombres négatifs et notaient abusivement un certain nombre complexe imaginaire  ; cela donna plus tard naissance à la théorie des nombres complexes.
Sur les autres projets Wikimedia :

Када-Мосто, Алоизий

путешественник
1432(1432)
Венеция
Италия
18 июля 1488(1488-07-18)
Ровиго
Алоизий Када-Мосто или Ка да Мосто Луиджи (Ca’ da Mosto, на португальском Luís Cadamosto bogner москва; около 1432, Венеция — 18 июля 1488, Ровиго) — путешественник.
Родился в Венеции, затем поступил на службу к португальскому инфанту Энрике Мореплавателю.
22 марта 1455 отплыл из Лагуша bogner москва, дошёл до Сенегамбии и по берегу до Зеленого мыса.
Объединившись с двумя другими судами, Када подошёл к устью Гамбии, но враждебное отношение туземцев заставило его вернуться в Португалию.
В 1456 он снова предпринял путешествие к берегам Гамбии, где и оставался до смерти инфанта Энрике (1460), после чего вернулся в отечество bogner одежда.
Скончался 18 июля 1488 в городе Ровиго, близ Венеции.
Первое, очень редкое издание описания его путешествия озаглавлено: «El libro de la prima navigazione per oceano a le terre de Negri della bassa Aethiopia» (Пиаченца, 1507 и 1519). Старинный немецкий перевод вышел в 1534 в Страсбурге: «Die New Welt. der Landschaften etc.».
Документы путешественника хранятся в en:Hakluyt Society “The Voyages of Cadamosto.” Series II Vol. LXXX. Year MCMXXXVII bogner москва.

Prātimokṣa

The Prātimokṣa (Sanskrit prātimokṣa) is a list of rules (contained within the vinaya) governing the behaviour of Buddhist monastics (monks or bhikṣus and nuns or bhikṣuṇīs)

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. Prāti means “towards” and mokṣa means “liberation” from cyclic existence (saṃsāra).
It became customary to recite these rules once a fortnight at a meeting of the sangha during which confession would traditionally take place. A number of prātimokṣa codes are extant, including those contained in the Theravāda, Mahāsāṃghika, Mahīśāsaka, Dharmaguptaka

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, Sarvāstivāda and Mūlasarvāstivāda vinayas. Prātimokṣa texts may also circulate in separate prātimokṣa sūtras, which are extracts from their respective vinayas.

The Prātimokṣa belongs to the Vinaya of the Buddhist doctrine and is seen as the very basis of Buddhism. On the basis of the Prātimokṣa there exist in Mahayana Buddhism two additional set of vows: The Bodhisattva vows and the Vajrayana vows. If these two set of vows are not broken, they are regarded as carrying over to future lives.
The Prātimokṣa is traditionally a section of the Vinaya. The Theravada Vinaya is preserved in the Pāli Canon in the Vinaya Piṭaka. The Mūlasarvāstivāda Vinaya is preserved in both the Tibetan Buddhist canon in the Kangyur, in a Chinese edition, and in an incomplete Sanskrit manuscript. Some other complete vinaya texts are preserved in the Chinese Buddhist canon (see: Taishō Tripiṭaka), and these include:
The Dharmaguptaka sect are known to have rejected the authority of the Sarvāstivāda pratimokṣa rules on the grounds that the original teachings of the Buddha had been lost.
The Patimokkha is the Pali equivalent of Prātimokṣa (Sanskrit). It is being followed by the monks of the Theravada lineage (Thailand, Sri Lanka, Myanmar, Cambodia and Laos). It consists of 227 rules for fully ordained monks (bhikkhus) and 311 for nuns (bhikkhunis). The Patimokkha is contained in the Suttavibhanga, a division of the Vinaya Pitaka.
Buddhist traditions in East Asia typically follow the Dharmaguptaka vinaya lineage of the prātimokṣa, and this is standard for the following Buddhist traditions:
Some traditions of Buddhism in Japan also carry out full monastic ordination, but most do not. Instead, these traditions of Japanese Buddhism have priests who take Bodhisattva vows but not full monastic vows (i.e. prātimokṣa).
The prātimokṣa of the Mulasarvastivada lineage followed in Tibetan Buddhism is taken for life unless one or more of the four root vows are broken. In Tibetan Buddhism, there are eight types of Prātimokṣa vows:
The lay prātimokṣa consists of five vows that are also known as the Five Śīlas:
One is not obliged to take all five vows

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. The commentaries describe seven types of lay followers:
Only full monks and full nuns are seen as full members of the buddhist monastic order. A group of four fully ordained monastics is seen as a sangha. The prātimokṣa tells also how to purify faults, how to solve conflicts and deal with all kinds of situations which can happen in the sangha.