#Isotopes in minerals
9 messages in this thread
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.
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
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
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
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.
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
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
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.
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.