. . "-345699"^^ . . . . . "14460"^^ . . "\u72C4\u6C0F\u5242"@zh . . . . . . "Dieldryna (\u0142ac. Dieldrinum) \u2013 syntetyczny insektycyd chlorowcoorganiczny. W \u015Brodowisku lub we wn\u0119trzu organizmu dieldryna powstaje po szybkim rozpadzie aldryny i ma do niej podobn\u0105 struktur\u0119 chemiczn\u0105. Jest ona trwa\u0142a w \u015Brodowisku i ulega bioakumulacji. Dieldryna jest wykorzystywana w rolnictwie do ochrony gleby i ziarna, przy kontrolowaniu populacji organizm\u00F3w przenosz\u0105cych choroby, takich jak komary i muchy tse-tse, w weterynarii jako \u015Brodek odka\u017Caj\u0105cy dla owiec oraz jako \u015Brodek konserwuj\u0105cy drewno i chroni\u0105cy produkty we\u0142niane przed molami. Wiele pa\u0144stw wprowadzi\u0142o ograniczenia b\u0105d\u017A zakazy dla stosowania dieldryny. Niekt\u00F3re kraje w dalszym ci\u0105gu zezwalaj\u0105 na ich import, m.in. dla cel\u00F3w ochrony przed termitami. Zwierz\u0119ta i ludzie mog\u0105 by\u0107 poddani dzia\u0142aniu dieldryny wskutek spo\u017Cycia ryb, owoc\u00F3w morza, nabia\u0142u, t\u0142ustych mi\u0119s i upraw korzeniowych hodowanych w zanieczyszczonej glebie lub wodzie. Dieldryna jest silnie toksyczna. Badania na zwierz\u0119tach wykaza\u0142y wp\u0142yw tego zwi\u0105zku na uszkodzenia w\u0105troby, zaburzenia funkcjonowania centralnego uk\u0142adu nerwowego i uk\u0142adu odporno\u015Bciowego. Zwi\u0105zek ten mo\u017Ce r\u00F3wnie\u017C zak\u0142\u00F3ca\u0107 gospodark\u0119 hormonaln\u0105. S\u0105 dowody na to, \u017Ce nara\u017Cenie w czasie ci\u0105\u017Cy powoduje uszkodzenia rozwijaj\u0105cych si\u0119 p\u0142od\u00F3w. Dieldryna wykazuje bardzo wysok\u0105 toksyczno\u015B\u0107 ostr\u0105 wobec organizm\u00F3w wodnych takich jak ryby, skorupiaki i p\u0142azy. Agencja Ochrony \u015Arodowiska w USA okre\u015Bla dieldryn\u0119 jako potencjalny \u015Brodek rakotw\u00F3rczy dla cz\u0142owieka."@pl . . . "Dieldrino estas , originale produktita kiel insekticido.La kemia formulo de dieldrino estas C12H8Cl6O. La molekulo havas ringan strukturon bazitan je naftalino. Dieldrino strikte rilatas al , kiu disi\u011Das mem al formo de dieldrino. Originale \u011Di estis evoluigita en la 1940-aj jaroj kiel alternativo al DDT. \u011Ci estas ekstreme rezista kemia\u0135o kaj malkombini\u011Das en la biosferon nur post tre longa tempo. \u011Ci povas akumuli\u011Di tra la nutro\u0109eno. \u011Ci pruvi\u011Dis venena por animaloj."@eo . . . "460784423"^^ . "Dieldrin"@nl . . . "La dieldrina \u00E9s un compost organoclorat originalment produ\u00EFt el 1948 per J. Hyman & Co a Denver com a insecticida per emprar en l'agricultura i que actualment est\u00E0 prohibida en totes les seves formulacions i usos per ser perjudicial per la salut humana i el medi ambient. Est\u00E0 relacionada amb l'aldr\u00EDn perqu\u00E8 aquest s'oxida f\u00E0cilment per convertir-se en dieldrina, i tant l'aldr\u00EDn com la dieldrina s\u00F3n anomenats a partir de la reacci\u00F3 amb la que se sintetitzen, ja que ambd\u00F3s s\u00F3n subst\u00E0ncies qu\u00EDmiques manufacturades no presents al medi ambient de manera natural. Originalment desenvolupada el 1940 com una alternativa al DDT, la dieldrina va demostrar ser un insecticida altament efica\u00E7 i va ser usada \u00E0mpliament des del 1950 fins a principis de 1970 quan va ser prohibit el seu \u00FAs a la majoria de pa\u00EFsos.La dieldrina forma part del grup de Contaminants org\u00E0nics persistents (COPs) definit pel conveni d'Estocolm. \u00C9s molt t\u00F2xic pels humans, pot absorbir-se per via cut\u00E0nia o ingesti\u00F3. La subst\u00E0ncia descompon en escalfar-se produint fums t\u00F2xics incloent clorur d'hidrogen. Reacciona amb \u00E0cids i oxidants. Ataca determinats metalls degut a la lenta formaci\u00F3 de clorur d'hidrogen."@ca . . "Dieldrin"@en . . "changed"@en . . "Dieldrin (systematick\u00FD n\u00E1zev (1aR,2R,2aS,3S,6R,6aR,7S,7aS)-3,4,5,6,9,9-hexachlor-1a,2,2a,3,6,6a,7,7a-oktahydro-2,7:3,6-dimethannafto[2,3-b]oxiren) je insekticid pou\u017E\u00EDvan\u00FD proti kl\u00ED\u0161\u0165at\u016Fm, mol\u016Fm a termit\u016Fm. Je to perzistentn\u00ED organick\u00E1 l\u00E1tka toxick\u00E1 i pro savce, a proto se vy\u017E\u00EDval i jako rodenticid. V b\u011B\u017En\u00FDch podm\u00EDnk\u00E1ch se jedn\u00E1 o b\u00EDlou krystalickou l\u00E1tku s teplotou t\u00E1n\u00ED 176 a\u017E 177 \u00B0C, ve vod\u011B t\u00E9m\u011B\u0159 nerozpustnou, m\u00EDrn\u011B rozpustnou v acetonu, slab\u011B v alkoholech. Po\u0161kozuje imunitn\u00ED a reproduk\u010Dn\u00ED syst\u00E9m, a proto byl v \u010Ceskoslovensku v roce 1980 zak\u00E1z\u00E1n. Mezin\u00E1rodn\u011B je regulov\u00E1n Stockholmskou \u00FAmluvou a tzv. POPs protokolem k Mezin\u00E1rodn\u00ED \u00FAmluv\u011B o zne\u010Di\u0161t\u011Bn\u00ED ovzdu\u0161\u00ED p\u0159esahuj\u00EDc\u00EDm st\u00E1tn\u00ED hranice (LRTAP)."@cs . . . . "Dieldrin"@en . . "Dieldrin, HEOD"@en . . "Dieldrina"@ca . . . "Dieldrin is an organochloride originally produced in 1948 by J. Hyman & Co, Denver, as an insecticide. Dieldrin is closely related to aldrin, which reacts further to form dieldrin. Aldrin is not toxic to insects; it is oxidized in the insect to form dieldrin which is the active compound. Both dieldrin and aldrin are named after the Diels-Alder reaction which is used to form aldrin from a mixture of norbornadiene and hexachlorocyclopentadiene."@en . . . "Dieldrino"@eo . . . "\u30C7\u30A3\u30EB\u30C9\u30EA\u30F3 (dieldrin) \u3068\u306F\u5143\u67651948\u5E74\u306B J. Hyman \u3068 Co, Denver \u306B\u3088\u3063\u3066\u6BBA\u866B\u5264\u3068\u3057\u3066\u88FD\u9020\u3055\u308C\u305F\u5869\u7D20\u5316\u70AD\u5316\u6C34\u7D20\u306E\u4E00\u3064\u3002\u30C7\u30A3\u30EB\u30C9\u30EA\u30F3\u306F\u30CA\u30D5\u30BF\u30EC\u30F3\u3092\u57FA\u672C\u3068\u3059\u308B\u74B0\u72B6\u69CB\u9020\u3092\u6709\u3059\u308B\u3002\u30A2\u30EB\u30C9\u30EA\u30F3\u304C\u52D5\u7269\u4F53\u5185\u3042\u308B\u3044\u306F\u571F\u58CC\u4E2D\u3067\u30A8\u30DD\u30AD\u30B7\u5316\u3055\u308C\u308B\u3053\u3068\u3067\u3082\u751F\u3058\u308B\u3002\u30A8\u30F3\u30C9\u30EA\u30F3\u3068\u306F\u7ACB\u4F53\u7570\u6027\u4F53\u3068\u306E\u95A2\u4FC2\u306B\u3042\u308B\u3002"@ja . . . . . . . . . . . "Dieldrin"@cs . . "La dieldrine est un insecticide organochlor\u00E9 qui a \u00E9t\u00E9 utilis\u00E9 comme une alternative au DDT. On a d\u00E9couvert par la suite que c'est une substance hautement toxique pour les organismes aquatiques et tr\u00E8s persistante dans le milieu naturel. En outre, elle provoque \u00E9galement de s\u00E9rieuses intoxications chez l'homme. Son utilisation doit donc rester aussi limit\u00E9e que possible.Sa dose l\u00E9tale 50 est de 40 mg\u00B7kg-1 (rat, oral).Son emploi dans l'agriculture en France fut interdit par arr\u00EAt\u00E9 le 2 octobre 1972."@fr . "Dieldrin-3D-balls.png"@en . . . . . . "Dieldrin (systematick\u00FD n\u00E1zev (1aR,2R,2aS,3S,6R,6aR,7S,7aS)-3,4,5,6,9,9-hexachlor-1a,2,2a,3,6,6a,7,7a-oktahydro-2,7:3,6-dimethannafto[2,3-b]oxiren) je insekticid pou\u017E\u00EDvan\u00FD proti kl\u00ED\u0161\u0165at\u016Fm, mol\u016Fm a termit\u016Fm. Je to perzistentn\u00ED organick\u00E1 l\u00E1tka toxick\u00E1 i pro savce, a proto se vy\u017E\u00EDval i jako rodenticid."@cs . . . "changed"@en . . . . . "\u72C4\u6C0F\u5242\uFF08Dieldrin\uFF09\u53C8\u540D\u5730\u7279\u9748\uFF0C\u662F\u4E00\u7A2E\u5DF2\u88AB\u8A31\u591A\u570B\u5BB6\u7981\u7528\u7684\u4EBA\u9020\u6BBA\u87F2\u5291\u3002\u7D14\u5730\u7279\u9748\u70BA\u767D\u8272\u7C89\u72C0\uFF0C\u5177\u6709\u7DE9\u6162\u7684\u63EE\u767C\u6027\uFF0C\u4E26\u4E14\u6709\u4E9B\u5FAE\u7279\u6B8A\u6C23\u5473\uFF0C\u5728\u6C34\u548C\u6CE5\u571F\u4E2D\u7686\u5177\u6709\u5F88\u5F37\u7684\u6301\u7E8C\u6027\uFF0C\u5C0D\u74B0\u5883\u5F71\u97FF\u6975\u5927\u3002"@zh . "La dieldrina \u00E9s un compost organoclorat originalment produ\u00EFt el 1948 per J. Hyman & Co a Denver com a insecticida per emprar en l'agricultura i que actualment est\u00E0 prohibida en totes les seves formulacions i usos per ser perjudicial per la salut humana i el medi ambient. Est\u00E0 relacionada amb l'aldr\u00EDn perqu\u00E8 aquest s'oxida f\u00E0cilment per convertir-se en dieldrina, i tant l'aldr\u00EDn com la dieldrina s\u00F3n anomenats a partir de la reacci\u00F3 amb la que se sintetitzen, ja que ambd\u00F3s s\u00F3n subst\u00E0ncies qu\u00EDmiques manufacturades no presents al medi ambient de manera natural."@ca . . . "Dieldrine"@fr . . . . . "Dieldrin ist ein zur Gruppe der Chlorkohlenwasserstoffe geh\u00F6rendes, nichtselektives Insektizid, das gegen Bodeninsekten und verschiedene krankheits\u00FCbertragende Insekten eingesetzt wurde. Au\u00DFerdem entsteht es als Abbauprodukt von Aldrin in Pflanzen und Tieren."@de . "(1aR,2R,2aS,3S,6R,6aR,7S,7aS)-3,4,5,6,9,9-hexachloro-1a,2,2a,3,6,6a,7,7a-octahydro-2,7:3,6-dimethanonaphtho[2,3-b]oxirene"@en . . . "Dieldrina"@it . . "Dieldrin is an organochloride originally produced in 1948 by J. Hyman & Co, Denver, as an insecticide. Dieldrin is closely related to aldrin, which reacts further to form dieldrin. Aldrin is not toxic to insects; it is oxidized in the insect to form dieldrin which is the active compound. Both dieldrin and aldrin are named after the Diels-Alder reaction which is used to form aldrin from a mixture of norbornadiene and hexachlorocyclopentadiene. Originally developed in the 1940s as an alternative to DDT, dieldrin proved to be a highly effective insecticide and was very widely used during the 1950s to early 1970s. Endrin is a stereoisomer of dieldrin. However, it is an extremely persistent organic pollutant; it does not easily break down. Furthermore, it tends to biomagnify as it is passed along the food chain. Long-term exposure has proven toxic to a very wide range of animals including humans, far greater than to the original insect targets. For this reason, it is now banned in most of the world. It has been linked to health problems such as Parkinson's, breast cancer, and immune, reproductive, and nervous system damage. It is also an endocrine disruptor, acting as an estrogen and antiandrogen, and can adversely affect testicular descent in the fetus if a pregnant woman is exposed to it."@en . . "Dieldrin is een gebrugde organische chloorverbinding met als brutoformule C12H8Cl6O. De stof komt voor als een kleurloos tot lichtbruin kristallijn poeder, dat slecht oplosbaar is in water."@nl . "Dieldryna (\u0142ac. Dieldrinum) \u2013 syntetyczny insektycyd chlorowcoorganiczny. W \u015Brodowisku lub we wn\u0119trzu organizmu dieldryna powstaje po szybkim rozpadzie aldryny i ma do niej podobn\u0105 struktur\u0119 chemiczn\u0105. Jest ona trwa\u0142a w \u015Brodowisku i ulega bioakumulacji."@pl . . "\u30C7\u30A3\u30EB\u30C9\u30EA\u30F3 (dieldrin) \u3068\u306F\u5143\u67651948\u5E74\u306B J. Hyman \u3068 Co, Denver \u306B\u3088\u3063\u3066\u6BBA\u866B\u5264\u3068\u3057\u3066\u88FD\u9020\u3055\u308C\u305F\u5869\u7D20\u5316\u70AD\u5316\u6C34\u7D20\u306E\u4E00\u3064\u3002\u30C7\u30A3\u30EB\u30C9\u30EA\u30F3\u306F\u30CA\u30D5\u30BF\u30EC\u30F3\u3092\u57FA\u672C\u3068\u3059\u308B\u74B0\u72B6\u69CB\u9020\u3092\u6709\u3059\u308B\u3002\u30A2\u30EB\u30C9\u30EA\u30F3\u304C\u52D5\u7269\u4F53\u5185\u3042\u308B\u3044\u306F\u571F\u58CC\u4E2D\u3067\u30A8\u30DD\u30AD\u30B7\u5316\u3055\u308C\u308B\u3053\u3068\u3067\u3082\u751F\u3058\u308B\u3002\u30A8\u30F3\u30C9\u30EA\u30F3\u3068\u306F\u7ACB\u4F53\u7570\u6027\u4F53\u3068\u306E\u95A2\u4FC2\u306B\u3042\u308B\u3002"@ja . . "La dieldrina es un plaguicida prohibido en todas sus formulaciones y usos por ser da\u00F1ino para la salud humana y el medio ambiente."@es . . . . "Dieldrin"@en . . . . . . . . . . . . "Dieldrin ist ein zur Gruppe der Chlorkohlenwasserstoffe geh\u00F6rendes, nichtselektives Insektizid, das gegen Bodeninsekten und verschiedene krankheits\u00FCbertragende Insekten eingesetzt wurde. Au\u00DFerdem entsteht es als Abbauprodukt von Aldrin in Pflanzen und Tieren."@de . "Dieldrin \u00E4r en biocid som togs fram 1948 i USA som ett alternativ till DDT. Dieldrin har i sin tur visat sig h\u00E4lsov\u00E5dligt och ersatts av eulan WW, som ocks\u00E5 visat sig v\u00E5dligt och blivit f\u00F6rbjudet i m\u00E5nga l\u00E4nder, inklusive Sverige. Environmental Protection Agency (EPA) i USA f\u00F6rbj\u00F6d anv\u00E4ndning av dieldrin inom jordbruket 1974; antitermitbehandling av tr\u00E4 stoppades frivilligt 1987. I Frankrike f\u00F6rbj\u00F6ds dieldrinanv\u00E4ndning 1972\u201310\u201302."@sv . . "Dieldrin"@en . . "Dieldrin"@sv . "D\u00E9-eildrin"@ga . . . . "Dieldryna"@pl . . "Dieldrin \u00E4r en biocid som togs fram 1948 i USA som ett alternativ till DDT. Dieldrin har i sin tur visat sig h\u00E4lsov\u00E5dligt och ersatts av eulan WW, som ocks\u00E5 visat sig v\u00E5dligt och blivit f\u00F6rbjudet i m\u00E5nga l\u00E4nder, inklusive Sverige. Environmental Protection Agency (EPA) i USA f\u00F6rbj\u00F6d anv\u00E4ndning av dieldrin inom jordbruket 1974; antitermitbehandling av tr\u00E4 stoppades frivilligt 1987. I Frankrike f\u00F6rbj\u00F6ds dieldrinanv\u00E4ndning 1972\u201310\u201302."@sv . . . "\u30C7\u30A3\u30EB\u30C9\u30EA\u30F3"@ja . . "Dieldrina"@es . . . "\u72C4\u6C0F\u5242\uFF08Dieldrin\uFF09\u53C8\u540D\u5730\u7279\u9748\uFF0C\u662F\u4E00\u7A2E\u5DF2\u88AB\u8A31\u591A\u570B\u5BB6\u7981\u7528\u7684\u4EBA\u9020\u6BBA\u87F2\u5291\u3002\u7D14\u5730\u7279\u9748\u70BA\u767D\u8272\u7C89\u72C0\uFF0C\u5177\u6709\u7DE9\u6162\u7684\u63EE\u767C\u6027\uFF0C\u4E26\u4E14\u6709\u4E9B\u5FAE\u7279\u6B8A\u6C23\u5473\uFF0C\u5728\u6C34\u548C\u6CE5\u571F\u4E2D\u7686\u5177\u6709\u5F88\u5F37\u7684\u6301\u7E8C\u6027\uFF0C\u5C0D\u74B0\u5883\u5F71\u97FF\u6975\u5927\u3002"@zh . . . "Is feithidic\u00EDd \u00ED an d\u00E9-eildrin ar comhdh\u00FAil org\u00E1nach de chuid an chl\u00F3ir\u00EDn \u00ED, cos\u00FAil leis an DDT. Th\u00E1inig s\u00ED an ch\u00E9ad uair in \u00FAs\u00E1id sna 1940id\u00ED, agus bh\u00EDt\u00ED an-d\u00F3chasach aisti ar dt\u00FAs, \u00F3 chreidt\u00ED go bhf\u00E9adfa\u00ED an DDT a chaitheamh i dtraipis\u00ED agus feithidic\u00EDd ab fhearr n\u00E1 \u00ED ar f\u00E1il. Faraor bh\u00ED an locht c\u00E9anna ar an d\u00E9-eildrin agus a bh\u00ED ar an DDT, n\u00F3 d\u00E9anann an d\u00E1 chomhdh\u00FAil carnadh sa bhiashlabhra. Thairis sin, t\u00E1 s\u00ED n\u00EDos cont\u00FAirt\u00ED don duine n\u00E1 an DDT f\u00E9in. Mar sin, d'\u00E9irigh an chuid ba mh\u00F3 de th\u00EDortha an domhain as an d\u00E9-eildrin a \u00FAs\u00E1id."@ga . . . . . "Is feithidic\u00EDd \u00ED an d\u00E9-eildrin ar comhdh\u00FAil org\u00E1nach de chuid an chl\u00F3ir\u00EDn \u00ED, cos\u00FAil leis an DDT. Th\u00E1inig s\u00ED an ch\u00E9ad uair in \u00FAs\u00E1id sna 1940id\u00ED, agus bh\u00EDt\u00ED an-d\u00F3chasach aisti ar dt\u00FAs, \u00F3 chreidt\u00ED go bhf\u00E9adfa\u00ED an DDT a chaitheamh i dtraipis\u00ED agus feithidic\u00EDd ab fhearr n\u00E1 \u00ED ar f\u00E1il. Faraor bh\u00ED an locht c\u00E9anna ar an d\u00E9-eildrin agus a bh\u00ED ar an DDT, n\u00F3 d\u00E9anann an d\u00E1 chomhdh\u00FAil carnadh sa bhiashlabhra. Thairis sin, t\u00E1 s\u00ED n\u00EDos cont\u00FAirt\u00ED don duine n\u00E1 an DDT f\u00E9in. Mar sin, d'\u00E9irigh an chuid ba mh\u00F3 de th\u00EDortha an domhain as an d\u00E9-eildrin a \u00FAs\u00E1id. Creidtear go bhfuil baint ag an d\u00E9-eildrin le galar Parkinson agus ailse na gc\u00EDoch, agus \u00ED ag d\u00E9anamh dochair do ch\u00F3ras imdh\u00EDonachta, c\u00F3ras at\u00E1irgthe agus n\u00E9arch\u00F3ras an duine. Le f\u00EDrinne t\u00E1 s\u00E9 cruthaithe go bhfuil s\u00ED n\u00EDos dochara\u00ED do na daoine agus do na mamaigh eile n\u00E1 do na feithid\u00ED f\u00E9in. T\u00E1 gaol dl\u00FAth ag an d\u00E9-eildrin leis an eindrin, feithidic\u00EDd eile den chine\u00E1l ch\u00E9anna, agus \u00ED ag d\u00E9anamh dam\u00E1iste d'org\u00E1nach an duine cos\u00FAil leis an d\u00E9-eildrin. Steir\u00E9-isim\u00E9ir\u00ED iad an d\u00E9-eildrin agus an eindrin, is \u00E9 sin n\u00EDl de dhifr\u00EDocht eatarthu ach strucht\u00FAr tr\u00EDthoiseach na m\u00F3il\u00EDn."@ga . . . . "Dieldrin is een gebrugde organische chloorverbinding met als brutoformule C12H8Cl6O. De stof komt voor als een kleurloos tot lichtbruin kristallijn poeder, dat slecht oplosbaar is in water."@nl . . . . "1881212"^^ . . . "La dieldrina o dieldrin \u00E8 un insetticida organoclorurato prodotto nel 1948 dalla J. Hyman & Co. di Denver. La dieldrina \u00E8 un'aldrina ossidata. Fu usata abbondantemente dagli anni cinquanta agli anni settanta ed il suo uso \u00E8 oggi proibito in molti paesi. Fa parte degli inquinanti organici persistenti. \u00C8 correlata all'insorgere della malattia di Parkinson, del cancro, di danni al sistema immunitario, riproduttivo, nervoso e ai ."@it . . . . . . . . . . "\u0414\u0438\u043B\u044C\u0434\u0440\u0438\u043D"@ru . . . . . "Dieldrino estas , originale produktita kiel insekticido.La kemia formulo de dieldrino estas C12H8Cl6O. La molekulo havas ringan strukturon bazitan je naftalino. Dieldrino strikte rilatas al , kiu disi\u011Das mem al formo de dieldrino. Originale \u011Di estis evoluigita en la 1940-aj jaroj kiel alternativo al DDT. \u011Ci estas ekstreme rezista kemia\u0135o kaj malkombini\u011Das en la biosferon nur post tre longa tempo. \u011Ci povas akumuli\u011Di tra la nutro\u0109eno. \u011Ci pruvi\u011Dis venena por animaloj."@eo . "La dieldrina es un plaguicida prohibido en todas sus formulaciones y usos por ser da\u00F1ino para la salud humana y el medio ambiente."@es . . "Dieldrin, HEOD"@en . . . . "\u0414\u0438\u043B\u044C\u0434\u0440\u0438\u043D \u2014 \u0445\u043B\u043E\u0440\u043E\u0440\u0433\u0430\u043D\u0438\u0447\u0435\u0441\u043A\u043E\u0435 \u0441\u043E\u0435\u0434\u0438\u043D\u0435\u043D\u0438\u0435, \u044D\u043F\u043E\u043A\u0441\u0438\u0434, \u043F\u0440\u043E\u0438\u0437\u0432\u043E\u0434\u043D\u043E\u0435 \u0430\u043B\u044C\u0434\u0440\u0438\u043D\u0430, \u0441\u0442\u0435\u0440\u0435\u043E\u0438\u0437\u043E\u043C\u0435\u0440 \u044D\u043D\u0434\u0440\u0438\u043D\u0430, \u0432\u044B\u0441\u043E\u043A\u043E\u0442\u043E\u043A\u0441\u0438\u0447\u043D\u043E\u0435 \u0432\u0435\u0449\u0435\u0441\u0442\u0432\u043E, \u043D\u0435\u043E\u0431\u044B\u0447\u0430\u0439\u043D\u043E \u0441\u0438\u043B\u044C\u043D\u044B\u0439 \u043C\u043D\u043E\u0433\u043E\u0441\u0442\u043E\u0440\u043E\u043D\u043D\u0438\u0439 \u0438\u043D\u0441\u0435\u043A\u0442\u0438\u0446\u0438\u0434, \u043E\u0434\u0438\u043D \u0438\u0437 \u0441\u0442\u043E\u0439\u043A\u0438\u0445 \u043E\u0440\u0433\u0430\u043D\u0438\u0447\u0435\u0441\u043A\u0438\u0445 \u0437\u0430\u0433\u0440\u044F\u0437\u043D\u0438\u0442\u0435\u043B\u0435\u0439."@ru . . . . "\u0414\u0438\u043B\u044C\u0434\u0440\u0438\u043D \u2014 \u0445\u043B\u043E\u0440\u043E\u0440\u0433\u0430\u043D\u0438\u0447\u0435\u0441\u043A\u043E\u0435 \u0441\u043E\u0435\u0434\u0438\u043D\u0435\u043D\u0438\u0435, \u044D\u043F\u043E\u043A\u0441\u0438\u0434, \u043F\u0440\u043E\u0438\u0437\u0432\u043E\u0434\u043D\u043E\u0435 \u0430\u043B\u044C\u0434\u0440\u0438\u043D\u0430, \u0441\u0442\u0435\u0440\u0435\u043E\u0438\u0437\u043E\u043C\u0435\u0440 \u044D\u043D\u0434\u0440\u0438\u043D\u0430, \u0432\u044B\u0441\u043E\u043A\u043E\u0442\u043E\u043A\u0441\u0438\u0447\u043D\u043E\u0435 \u0432\u0435\u0449\u0435\u0441\u0442\u0432\u043E, \u043D\u0435\u043E\u0431\u044B\u0447\u0430\u0439\u043D\u043E \u0441\u0438\u043B\u044C\u043D\u044B\u0439 \u043C\u043D\u043E\u0433\u043E\u0441\u0442\u043E\u0440\u043E\u043D\u043D\u0438\u0439 \u0438\u043D\u0441\u0435\u043A\u0442\u0438\u0446\u0438\u0434, \u043E\u0434\u0438\u043D \u0438\u0437 \u0441\u0442\u043E\u0439\u043A\u0438\u0445 \u043E\u0440\u0433\u0430\u043D\u0438\u0447\u0435\u0441\u043A\u0438\u0445 \u0437\u0430\u0433\u0440\u044F\u0437\u043D\u0438\u0442\u0435\u043B\u0435\u0439."@ru . "La dieldrina o dieldrin \u00E8 un insetticida organoclorurato prodotto nel 1948 dalla J. Hyman & Co. di Denver. La dieldrina \u00E8 un'aldrina ossidata. Fu usata abbondantemente dagli anni cinquanta agli anni settanta ed il suo uso \u00E8 oggi proibito in molti paesi. Fa parte degli inquinanti organici persistenti. \u00C8 correlata all'insorgere della malattia di Parkinson, del cancro, di danni al sistema immunitario, riproduttivo, nervoso e ai ."@it . . "La dieldrine est un insecticide organochlor\u00E9 qui a \u00E9t\u00E9 utilis\u00E9 comme une alternative au DDT. On a d\u00E9couvert par la suite que c'est une substance hautement toxique pour les organismes aquatiques et tr\u00E8s persistante dans le milieu naturel. En outre, elle provoque \u00E9galement de s\u00E9rieuses intoxications chez l'homme. Son utilisation doit donc rester aussi limit\u00E9e que possible.Sa dose l\u00E9tale 50 est de 40 mg\u00B7kg-1 (rat, oral).Son emploi dans l'agriculture en France fut interdit par arr\u00EAt\u00E9 le 2 octobre 1972."@fr . "Dieldrin"@de . . . . . "Dieldrin.svg"@en . . . "1121653554"^^ . .