CompuServe Thread

#Isotopes in minerals

9 messages in this thread
#170512From: Jon WoolfFeb 25, 1995 8:32 PM
I have a question concerning the formation of mineral crystals during the process of igneous rock formation. I've seen people claim (or appear to claim) that "fractional distillation" can alter isotopic ratios so that minerals that solidify at different temperatures, or over different time spans, have different isotope ratios, thus screwing up the ratios so critical to radiometric dating. As I understand this, they mean that if you take (say) a strontium-bearing mineral from the central area of a large intrusion, and another strontium-bearing mineral from near the edge of the same intrusion, they will have different ratios of the various strontium isotopes. Now, I've always heard and read that minerals' isotopic ratios are a constant, that inorganic chemical processes don't and in fact can't differentiate between isotopes. If you take two samples from the same igneous intrusion, they _will_ have the same isotope ratios, except for changes due to radioactive decay after the melt solidified. I think the "fractional distillation" claim is all wet, but I'm not certain. Can anyone here set me straight on this? Thanks. Jon W.
#170583From: Kamron KirkconnellFeb 26, 1995 8:10 AM
Jon I have a different process that may explain(some/many/all) deposits veins and ore intrusions. Well after the formation of the earth the molten materials stratified into layers of materials based on densities. These are just approximate guesses but the layers were in solid and liquid layers stratified by densities. Under the crust which is 8 miles thick give or take there are layers quartz/granite, Basalt/feldspar/granite, then the metals, then the core. The crust under went major catastrophes or one big where the entire crust was shattered vertically and horizontally throughout. These cracks would open up to great depths at times and would be flooded with materials from these layers. As the cracks worked back and forth different amounts of mixing would occur and the materials would be injected into cracks and spaces as well as pushed up towards the surface at times blasted out the top of the crack as a mixture of gases that would condense and rain down on the land. A simplistic view of a fantastic mechanism that could explain all the combinations of materials we find on the earth. You are in it much deeper than I am but this is a thought I have had wondered how it would run in your mental simulator. Kamron
#171228From: Norman ReitzelMar 1, 1995 9:33 AM
Kamron, Take a physical chemistry course. Then look at phase rules in the face of pressures of kilobars. You will find that the Gibbs energies are quite high enough to favor segregation of minerals into separate aggregates. Oh, another thing. A lot of underground minerology is in solution, with the respective fluids being CO2 and H2O – which are -NOT- miscible at high pressures. Quartz in particular is very often deposited from such superfluid vapors. — Norm
#170704From: Doug MitchellFeb 26, 1995 7:41 PM
Hi, Jon– I would expect _slightly_ older datings from the outer edges of an igneous intrusion than in the center, but not because of some isotopic fractionation. The outer regions should generally be the first to cool and solidify, being exposed to a nice heat sink in the form of surrounding rocks. Are these people claiming greater radiodate differences than this? One method of separating heavy water from water is to distill it (keeping only the last water to condense) over and over and over and over… ad nauseum. The amount of water discarded relative to the product is awesome and the efficiency is appalling. Distillation can distinguish isotopes, but it is an extremely weak distinction, and would be even weaker for the heavier atoms used in radiodating. D2O and H2O differ in weight by a "hefty" ratio of about 20/18, where K40 and K39 would be a quarter as distinguishable by weight (40/39). It surely cannot be much compared to the basic isotope ratios that radiodating depends on, unless there were reason to expect many repetitions of the distillation. This distillation effect would have to alter ratios of stable isotopes just as easily if the weight difference is similar. If I see constant (within the intrusion) ratios of stable isotopes, I see no reason to imagine radioisotope ratios were variable. If I read an aged chart of nuclides correctly, original K40/K41 anomalies should be accompanied by much stronger K39/K41 anomalies (both appear to be stable isotopes). –Doug
#170756From: Jon WoolfFeb 26, 1995 9:45 PM
Doug, Thanks for the reply. That's about what I figured, but I wanted to hear it from somebody who knew the subject better than I do. >> D2O and H2O differ in weight by a "hefty" ratio of about 20/18, where K40 and K39 would be a quarter as distinguishable by weight (40/39). << And the difference would be even less with heavier isotopes, right? U238 and U235; the various isotopes of strontium; different isotopes of lead; and so on. Jon W.
#171129From: Doug MitchellFeb 28, 1995 11:01 PM
Hi, Jon– Right, I picked K40 because it was the lightest radioisotope used in geological dating (C14 is for archaeologists, mostly) I could think of; Rb/Sr are worse and U/Th still worse. Sr has lots of stable isotopes to take ratios among and keep the Rb-decay product (Sr87, I think) ratio honest. The only thing I do not know is how often daters use these stable-isotope cross-checks. If they use mass spectrometers, these comparisons should be real easy to toss in. –Doug
#171229From: Norman ReitzelMar 1, 1995 9:33 AM
Jon, I looked once for K39/K40 segregation in the Llano uplift batholith. I had core samples from 3100 meters bearing K rich alkali feldspars, and similar samples from intrusive dikes from the San Saba (edge of uplift) area. To within 0.07%, the isotopic composition is identical. Note that I'm not saying that the two were different by that amount – my instrument (a Finigan quadrapole mass spectrometer) was good to this amount, and as far as I could tell, the isotope ratios were dead on. Having said that, I will tell you that one sometimes sees deuterium differentiation of a few ppm in amphibolite rocks. As Doug points out, deuterium is the most likely isotope to show fractionation, and sure enough if you look (hard) you can see some evidence, down at the limits of detectability. Amphiboles that were created by contact metamorphosis seem to have higher deuterium ratios than those created by regional metamorphosis. The difference is like 0.014723 to 0.014729 in the most differentiated samples I've heard of. — Norm
#171004From: Daniel J. LynchFeb 28, 1995 1:14 PM
Where does this claim of fractional-distillation in magmas come from? Distillation involves vaporization of the "fractionated" material and that doesn't happen in earth temperature processes. Partial melting and fractional CRYSTALLIZATION are processes that take place in the earth within or beneath the crust. In partial melting, the least strongly bonded atoms (ions) are dislodged from crystals at temperatures near melting and when enough of these loose ions have collected together to move as a body, you have a magma. One foundation of isotope geochemistry is that these magma bodies evolve in a homogeneous fashion. Fractional crystallization selectively extracts the constituents that form the highest melting point minerals and magma (the remaining liquid) composition changes over time (remember Bowen?). This is well known in volcanoes that have erupted sequences of lavas over periods of time, the rocks fall into compositional series like basalt to andesite to trachyte. Isotope ratios of Strontium and Neodymium in these lavas indicate concentrations of parental Rubidium and Samarium in the source rocks from which the magma was derived identifying them as mantle or crust or mixed. Even if it is theoretically possible for the heavy isotopes (masses ranging from 86 to 238) to fractionate, there are vast numbers of isotope studies that are internally consistent so the effect is well below experimental error. Although isotopic ratios can indicate age, they are mostly used as indicators of petrologic process. Potassium-Argon is used to determine the ages of igneous rocks that can be assumed to have crystallized with no 40-Argon or with a small amount of argon entrapped from the atmosphere. Any 40-Argon found over this background comes from the decay of 40 Potassium in the rock and the relative amounts indicate the time since cooling (if none has been lost). This works amazingly well with most volcanic rocks. Dan Lynch, formerly of U of Arizona's Isotope Geochemistry Lab.
#171044From: Jon WoolfFeb 28, 1995 5:38 PM
Daniel, >> Where does this claim of fractional-distillation in magmas come from? << Mea culpa. I went back and checked, and the fella who made this claim did indeed use the term "fractional crystallization." Sorry for the goof. So far, the tide seems to be flowing strongly against this claim that fractional-crystallization could mess up the isotope ratios, and thus mess up radiometric dating techniques. Jon W.