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Isotope geochronology: models versus reality. Invited lecture presented at the 12th geochronological conference “Dating of minerals and rocks XII”, UMCS, Lublin, 16.10.2014

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A N N A L E S

U N I V E R S I T A T I S M A R I A E C U R I E - S . à 2 ' 2 : S . A

L U B L I N – 3 2 L 2 N I A

V2L L;I; SECTI2 AAA 2014

IS2T23E *E2C+R2N2L2*<

M2'ELS VERSUS REALIT<

INVITED LECTURE PRESENTED AT THE 12TH

GEOCHRONOLOGICAL CONFERENCE “DATING OF MINERALS AND ROCKS XII”, UMCS, LUBLIN, 16.10.2014

Jan Burchart

3roIessor emeritus, Institute oI *eoloJical Sciences, 3olish AcaGem\ oI Sciences, TwarGa 1, 00-1 :arsaw; e-mail MEurchart1#uScSoc]taSl

ABSTRACT

MaMorit\ oI the SaSers on isotoSic GatinJ oI minerals anG rocks have Eeen GevoteG to some new JeochronoloJical Gata imSortant Ior JeoloJ\ or to GeveloSments oI aSSaratus anG imSrovements oI laEorator\ techniTues anG SroceGures +owever, there are some Easic SroElems concerninJ creGiEilit\ oI the Gata SuElisheG incluGinJ the ³error Erack-ets´ , anG their JeoloJical meaninJ, which rarel\ are toucheG on

The issues to Ee raiseG ma\ Ee JrouSeG into two cateJories 1 Gistortion in the course oI SreSarator\ oSerations anG Iinal measurements, anG 2 some GouEts concern-inJ JeoloJical interSretation oI the Gata anG the moGels useG )irst oI all it shoulG Ee reali]eG that what we reall\ anal\se in a sSectrometer is not an e[istinJ rock or mineral Eut a SowGer SroGuceG E\ man\ steSs oI consecutive SroceGures, each oI them caSaEle oI irreversiEl\ GistortinJ the oriJinal comSosition

Keywords: isotoSe JeochronoloJ\, moGels, GatinJ, mass sSectrometr\, uncertaint\ The routine seTuence oI oSerations EeJins with crushinJ anG JrinGinJ, when a selective Sulverisation attacks IelGsSars much more than micas – not to men-tion Tuart] The resultinJ moGiIicamen-tion oI the oriJinal comSosimen-tion ma\ Ee ver\

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116 J. BURC+ART

______________________________________________________________________

suEstantial Ior whole-rock samples. Special care anG microscopic control are necessary when aJe homoJeneity may Ee suspecteG. This is the case oI miJmatites anG other non-homoJeneous rocks e.J. paleovolcanites consistinJ oI relic pyro[enes surrounGeG Ey seconGary chlorites, or rocks with well-GevelopeG reaction ]ones . The proElem oI homoJeneity applies also to separateG minerals, which oIten contain tiny inclusion oI minerals GiIIerinJ in isotopic composition anG/or aJe. Simple sievinJ may result in complete loss oI tiny ]ircon Jrains in Iavour oI larJe ones, the process stronJly GistortinJ the composition oI the entire ]ircon population which oIten is a mi[ture, not only oI si]es Eut also aJes.

:hile the aIoresaiG eIIects seem to Ee important only in some special cases, the Maw-crusher ³memory´ constitutes uEiTuitous GanJer oI serious, thouJh unGervalueG, contamination oI the whole-rock samples. Even the most careIul cleaninJ oI any Maw-crusher cannot Juarantee that the machine Eecomes aEso-lutely GevoiG oI any traces oI a previously treateG rock. There are too many re-cesses, nooks, scratches anG some surIace imperIections. A siJniIicance oI such an eIIect was testeG Ey a simple e[periment >1@: the 87Sr/86Sr ratio was measureG

in a 3recamErian Jneiss anG a Jurassic limestone in two seTuences Jneiss – limestone – Jneiss, anG limestone – Jneiss – limestone . Contamination oI the limestone JranulateG aIter the Jneiss was insiJniIicant, while the eIIect was very serious Ior the Jneiss JranulateG aIter the limestone, the GiIIerence Eetween the two rocks in the Sr aEunGances EeinJ the likely e[planation. It appears that the maJnituGe oI the contamination GepenGs on three parameters: the ratio oI the mass oI contaminatinJ matter Girt or some remnants oI the previous rock to the mass oI the sample; the ratio oI the element concentrations; anG the ratio oI the isotope ratios to Ee measureG. It turneG out that when the consecutive rocks are very GiIIerent in the isotope ratios the eIIect may aIIect the rG Gecimal place

even at very careIul cleaninJ. ThereIore, not only thorouJh cleaninJ Eut also a rational seTuence oI rocks is stronJly recommenGeG. An isotopic analysis oI a Tertiary Easalt crusheG aIter a 3recamErian Jneiss may Ee completely worthless even at the most sterile chemical operations anG a very hiJh precision oI the spectrometric measurements. It shoulG Ee stresseG that contamination introGuceG in the course oI preliminary operations is irreversiEle anG it Gecisively inIlu-ences the Iinal spectrometric values. BesiGes, it is GiIIicult to Getect, assess Tuan-titatively, anG make proper corrections. Contamination may occur also in the course oI consecutive chemical operations anG it can aIIect cleanness oI water, reaJents, vessels, air, reliaEility oI the spike solutions anG their staEility, eIIi-ciency oI chromatoJraphic separation – Eut that is relatively easy to Getect, as-sess anG reGuce.

3uElications concerninJ the maJnituGe oI errors preIeraEly ³uncertainties´ are aEunGant, Eut almost completely restricteG to spectrometric analyses. Actual-ly the apparentActual-ly preciseActual-ly GetermineG error Erackets e[presseG Ey ³“´ relateG to an aJe comprise the spectrometric errors only. It is true that only such

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uncertain-ISOTO3E *EOC+RONOLO*<: MODELS VERSUS REALIT<« 117

ties can Ee precisely GetermineG. +owever, we are GeluGeG Ey apparently hiJh precision oI an analysis, while the spectrometric error shoulG Ee Jrossly enlarJeG Ey the errors oI GiIIerent parentaJe, iI they are to Ee unGerstooG as uncertainty oI aJe.

Various moGels so Iar introGuceG usually are e[presseG in a Iorm oI isochrone GiaJrams. The initial ratio is either taken Irom minerals GevoiG oI the raGioactive nucliGe, or oEtaineG Ey the least sTuares methoG. +owever, as point-eG Ey =henJ >2@ to accept such a calculatpoint-eG value, anG to take it Ior Jrantpoint-eG Ior a series oI whole rock samples sometimes may Ee an oversimpliIication in view oI the processes oI IractionateG crystallisation, partial meltinJ, mi[inJ, or meta-morphism. An assumption oI a perIect homoJeneity oI the isotopic ratios in rocks at the initial moment is clearly relateG to the scale oI the oEMect. It may Ee acceptaEle Ior a ranJe oI meters, Eut seems improEaEle Ior a larJe EoGy oI anatectic oriJin. ConseTuently it is relateG to the samplinJ pattern anG its con-scious choice.

The analytical Gata representinJ isotopic ratios are converteG to an ³aJe´ value e[presseG in years Ey means oI a tacitly assumeG moGel. ThereIore, in orGer to oEtain a reliaEle aJe value it is not enouJh to carry out the analytical operations with the Jreatest possiEle care Eut also to Ee conIiGent oI the proper moGel applieG, a moGel which e[presses the Jeochemical evolution oI the rock e[amineG.

It touches upon the proElem oI what we Gate. )or a JeoloJist an aJe oI a rock relates to the rock¶s position in the architecture oI the comple[. It is an aJe oI the Iorm, not suEstance. SeTuence oI rock layers, intrusive contacts, cross-cuttinJ oI veins or microtectonic elements – all the classical tools oI JeoloJy – reIers to the Iorms. On the other hanG, the isotope Jeochemistry stuGies the matter only, GisreJarGinJ the Iorms oI occurrence. Thus there is a suEstantial GiIIerence as reJarGs the oEMect oI an analysis, anG conseTuently it may Ee the source oI misunGerstanGinJ. AnaloJous misunGerstanGinJ appears when a cool-inJ aJe is tacitly reJarGeG as an aJe oI crystallisation.

Another remark is relateG to the moGels useG to GescriEe the evolution oI NG-Sm system. The Easis oI the moGel are the CHUR or DM values taken as the initial ratios. ConseTuently the very iGea oI the aJe oI a rock Eecomes ElurreG. The ³aJe´ value oEtaineG is relateG to the isotopic evolution oI the matter which later Eecame soliGiIieG as the rocks. By no means it may Ee treateG as the aJe oI a rock. Sometimes it is laEelleG as a crust-formation age thouJh some authors raiseG GouEts which resulteG in the two-staJe moGels.

A process oI JeoloJical interpretation oI the isotopic Gata is EaseG on com-parison oI the Gata with the moGel e[pectation which is only a simpliIication oI the processes which actually occurreG in nature. Such an approach stems Irom the principle oI uniIormity. +owever, the proElem Eecomes GisputaEle when we proceeG to very Gistant times anG Gepth ]ones. Certainly our knowleGJe oI the

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118 J. BURC+ART

______________________________________________________________________

processes which operateG GurinJ 3recamErian times is GeIinitely insuIIicient. It especially applies to the processes actinJ within the mantle, anG the e[chanJe reactions Eetween the mantle anG the crust. +ave such processes Eeen constant Ior the last 4.6 Eillion years" +ow Iar Eack in time are we entitleG to apply the JeoloJy-EaseG moGels to ³pre-JeoloJical´ times" These are somewhat perple[-inJ Tuestions to which it is GiIIicult to Jive a well-JrounGeG answer. :ithout it, any petroJenetic interpretations oI the Sm-NG or Lu-+I systems remain nothinJ more than workinJ hypotheses, purely theoretical moGels.

Certainly the moGels we use as a Easis Ior GatinJ are Jross simpliIication as compareG to the comple[ anG poorly recoJniseG processes which unGerwent in nature. This lecture was EaseG on some e[cerpts Irom a monoJraph Ey J. Burchart anG J. .ral Isotope record of the Earth’s past in 3olish Izotopowy

]DSLVSU]HV]áRĞFL=LHPL) prepareG Ior puElication.

RE)ERENCES

1. Burchart J., BachliĔski R. 2000) .RQWDPLQDFMD SUyEHN VNDá Z WUDNFLH NUXV]HQLD

i mielenia. V OJylnopolska SesMa Naukowa ÄDatowanie Mineraáyw i Skaá´, .rakyw

10-12.02.2000, 2-4.

2. =henJh <.). 1989) Influences of the nature of the initial Rb-Sr system on isochron

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