Isotope Geochemistry

Isotopes
• Isotopes have different ## of neutrons,
and thus a different mass
• Affect on reactions in small, but real, and
provides another measurement of
reactions – affected by similar
physicochemical parameters!
• Also a critical tracer – the isotopes can be
used to track molecules in a reaction!
 Fractionation
• A reaction or process which selects for
one of the stable isotopes of a particular
element
• If the process selects for the heavier
isotope, the reaction product is ‘heavy’, the
reactant remaining is ‘light’
• Isotope fractionation occurs for isotopic
exchange reactions and mass-dependent
differences in the rates of chemical
reactions and physical processes
 Fractionation Factor, 
• R is the ratio of heavy to light isotopes
• , or fractionation factor, is the ratio between
reactant and product
Rreac tan ts

R products
 Why a ratio???
• Differences between 2 isotopes of one
element is VERY small – to measure them
individually with enough precision is difficult
to impossible for most isotope systems
• By comparing a sample ratio to a standard
ratio, the difference between these two can
be determined much more precisely!!
 Isotope Standards
• VSMOW – Vienna Standard Mean Ocean
Water – bunch of ocean water kept in
Austria – O and H standard
• PDB – Pee Dee Belemnite – fossil of a
belemnite from the Pee Dee formation in
Canada – C and O
• CDT – Canyon Diablo Troilite –meteorite
fragment from meteor crater in Arizona,
contains FeS mineral Troilite – S
• AIR – Atmospheric air - N
 Measuring Isotopes
• While different, isotopes of the same element
exist in certain fractions corresponding to
their natural abundance (adjusted by
fractionation) a Ra Where R is the ratio of
a
b  heavy/light isotope and  is
Rb the fractionation factor

• We measure isotopes as a ratio of the

isotope vs. a standard material (per mille ‰)
 Rsample  Rstandard 
 O  
18
 103
 Rstandard  ‰
3 a a
10 ln    a   b  
b b
 is “delta”, and is the isotope ratio of a particular
thing (molecule, mineral, gas) relative to a
standard times 1000. sometimes called ‘del’
 Rsample  Rstandard 
 O  
18
  103
 Rstandard 
 is “delta” and is the difference between two
different isotope ratios in a reaction:
 = A - B
Many isotopers are very sensitive about misuses of isotope terminology.
Harmon Craig’s immortal limerick says it all:
There was was a young man from Cornell
Who pronounced every "delta" as "del"
But the spirit of Urey
Returned in a fury
And transferred that fellow to hell
Equilibrium vs. Kinetic fractionation
• Fractionation is a
reaction, but one in which
the free energy
differences are on the
order of 1000x smaller
than other types of
chemical reactions
• Just like other chemical
reactions, we can
describe the proportion of
reactants and products as
an equilibrium or as a
kinetic function
Because the kinetic energy for heavy and light
isotopes is the same, we can write:
vL mH

vH mL
In the case of 12C16O and 13C16O we have:
vL 28.99827
  1.0177
vH 27.994915
Regardless of the temperature, the velocity of
C O is 1.0177 times that of 13C16O, so the
12 16

lighter molecule will diffuse faster and

evaporate faster.
 Equilibrium Fractionation
• For an exchange reaction:
½ C16O2 + H218O ↔ ½ C18O2 + H216O
• Write the equilibrium: 1
(C 18O2 ) ( H 16O2 )
2
K 1
(C 16O2 ) ( H 18O2 )
2

• Where activity coefficients effectively cancel

out
• For isotope reactions, K is always small,
usually 1.0xx (this K is 1.047 for example)
 WHY IS K DIFFERENT FROM
1.0?
Because 18O forms a stronger covalent bond
with C than does 16O.
The vibrational energy of a molecule is given by
the equations:
1 k
Evibrational  1
2 h  F   kx
2 m
O Thus, the frequency of vibration depends
H H on the mass of the atoms, so the energy
of a molecule depends on its mass.
• The heavy isotope forms a lower energy
bond; it does not vibrate as violently.
Therefore, it forms a stronger bond in
the compound.
• The Rule of Bigeleisen (1965) - The
heavy isotope goes preferentially into
the compound with the strongest bonds.
 Temperature effects on
fractionation
• The fractionation factors, , are affected by T
(recall that this affects EA) and defined
empirically:
6 Where A and B are constants
A  10
103 ln  ba  2
B determined for particular reactions
T and T is temp. in Kelvins
• Then,
3 a a
10 ln    a   b  
b b
• As T increases,  decreases – at high T 
goes to zero
 FRACTIONATION DURING
PHYSICAL PROCESSES
• Mass differences also give rise to fractionation
during physical processes (diffusion,
evaporation, freezing, etc.).
• Fractionation during physical process is a
result of differences in the velocities of isotopic
molecules of the same compound.
• Consider molecules in a gas. All molecules
have the same average kinetic energy, which
is a function of temperature.
2
Ekinetic  1
2 mv
Using isotopes to get information on
physical and chemical processes
• Fractionation is due to some reaction,
different isotopes can have different
fractionation for the same reaction, and
different reactions have different
fractionations, as well as being different at
different temperatures and pressures
• Use this to understand physical-chemical
processes, mass transfer, temperature
changes, and other things…
 Equilibrium Fractionation II
• For a mass-dependent reaction:
• Ca2+ + C18O32-  CaC18O3
• Ca2+ + C16O32-  CaC16O3
• Measure 18O in calcite (18Occ) and water
(18Osw)
• Assumes 18O/16O between H2O and CO32- at
some equilibrium
T ºC = 16.998 - 4.52 (18Occ - 18Osw) + 0.028 (18Occ-18Osw)2
 Empirical Relationship between Temp. &
Oxygen Isotope Ratios in Carbonates

At lower temperatures, calcite

crystallization tends to incorporate a
relatively larger proportion of 18O
because the energy level (vibration)
of ions containing this heavier isotope
decreases by a greater amount than ions
containing 16O.

As temperatures drop, the energy level

of 18O declines progressively by an
amount that this disproportionately
greater than that of the lighter 16O.
 Distillation
• 2 varieties, Batch and Rayleigh distillation
dependent on if the products stay in contact and
re-equilibrate with the reactants
• Batch Distillation:
f = i – (1 – F) 103lnCO2-Rock
where the isotope of the rock (i) depends on
it’s initial value (f) and the fractionation factor
• Rayleigh Distillation
f - i =103(F( – 1) – 1)
 RAYLEIGH DISTILLATION
Isotopic fractionation that occurs during
condensation in a moist air mass can be
described by Rayleigh Distillation. The equation
governing this process is:
o  1
Rv  Rv f
where Rv = isotope ratio of remaining vapor, Rv° =
isotope ratio in initial vapor, ƒ = the fraction of
vapor remaining and a = the isotopic
fractionation factor
Effect of Rayleigh
distillation on the
18O value of water
vapor remaining in
the air mass and of
meteoric precipitation
falling from it at a
constant temperature
of 25°C.
Complications:
1) Re-evaporation
2) Temperature
dependency of 
 ISOTOPE FRACTIONATION IN THE
HYDROSPHERE
Evaporation of surface water in equatorial regions
causes formation of air masses with H2O vapor
depleted in 18O and D compared to seawater.
This moist air is forced into more northerly, cooler air
in the northern hemisphere, where water
condenses, and this condensate is enriched in 18O
and D compared to the remaining vapor.
The relationship between the isotopic composition of
liquid and vapor is:
 Ol    Ov  10   10
18 l
v
18 3 3
Assuming that 18Ov = -13.1‰ and vl(O) =
1.0092 at 25°C, then
 Ol  1.0092 13.1  10   10  4.0 0 00
18 3 3

and assuming Dv = -94.8‰ and vl(H) = 1.074 at

25°C, then
Dl  1.074 94.8  103   103  27.8 0 00
These equations give the isotopic composition of
the first bit of precipitation. As 18O and D are
removed from the vapor, the remaining vapor
becomes more and more depleted.
Thus, 18O and D values become increasingly
negative with increasing geographic latititude
(and altitude.
Map of North
America
showing
contours of the
approximate
average D
values of
meteoric surface
waters.
Because both H and O occur together in water, 18O and D
are highly correlated, yielding the meteoric water line
(MWL): D  818O + 10
 Deviation from MWL
• Any additional fractionation process which
affects O and D differently, or one to the
exclusion of the other will skew a water
away from the MWL plot
• These effects include:
– Elevation effects - (D -8‰/1000m, -4‰/ºC)
– Temperature ( different!)
– Evapotranspiration and steam loss
– Water/rock interaction (little H in most rocks)
 Iron Isotopes
Earth’s Oceans 3 Ga had no
oxygen and lots of Fe2+,
cyanobacteria evolved,
produced O2 which oxidized
the iron to form BIFs – in time
the Fe2+ was more depleted
and the oceans were stratified,
then later become oxic as they This interpretation is largely based on iron
are today isotopes in iron oxides and sulfide minerals
deposited at those times (Rouxel et al., 2005)
 Experiments
• Fe2+ and
FeSmackinawite at
equilibrium,
separate physically
(filter) and measure
each component:

From Butler et al., 2005 EPSL 236 430-442

Fe –isotope exchange with a particle
Fe2+
• Particles coarsen via Fe2+ Fe2+
Fe2+ Fe
2+
Fe2+
Ostwald ripening or Fe2+
topotactic alignment – Fe 2+ Fe2+ Fe2+

how fast can isotopes Fe2+

exchange with Fe in a
xstal actively getting
bigger?
• At certain size internal
Fe2+ does not
exchange…
Guilbaud et al., 2010 EPSL 300 174-183
 What can we get from using
multiple isotopes?
• Many isotope systems have more than 2
stable isotopes – 56Fe, 57Fe, 58Fe; 32S, 33S,
34
S, 36S
• Looking at multiple isotopes can provide
new insight on multiple processes,
especially useful for complicated reaction
pathways, also helps get at equilibrium v.
kinetic processes, and mass-dependent v.
independent processes…
 • Tracing S-isotopic fractionation from
different communities of organisms (Sulfate-
reducers, sulfur disproportionation,
phototrophic S oxid.)

From Zerckle et al., 2009 GCA 73, 291-306

 S isotopes and microbes
• The fractionation of H2S formed from bacterial
sulfate reduction (BSR) is affected by several
processes:
– Recycling and physical differentiation yields
excessively depleted H2S
– Open systems – H2S loss removes 34S
– Limited sulfate – governed by Rayleigh process,
enriching 34S
– Different organisms and different organic substrates
yield very different experimental 34S
• Ends up as a poor indicator of BSR vs. TSR
 Mass-independent fractionation
• Mass effects for 3 stable isotopes
(such as 18O, 17O, and 16O) should
have a mass-dependent relationship
between each for any process
• Deviation from this is mass-
independent and thought to be
indicative of a nuclear process
(radiogenic, nucleosynthetic,
spallation) as opposed to a physico-
chemical process
• Found mainly associated with
atmospheric chemistry, effect can be
preserved as many geochemical
reactions in water and rock are mass-
dependent
 S-isotopic evidence of Archaen
atmosphere
• Farquar et al., 2001; Mojzsis et al., 2003
found MIF signal in S isotopes (32S, 33S,
34
S) preserved in archaen pyrites
precipitated before 2.45 Ga
• Interpreted to be signal from the photolysis
of SO2 in that atmosphere – the reaction
occurs at 190-220nm light, indicating low
O2 and O3 (which very effficiently absorb
that wavelength)
 Volatilization
• calcite + quartz = wollastonite + carbon dioxide
CaCO3 + SiO2 = CaSiO3 + CO2
• As the CO2 is produced, it is likely to be expelled
• Other volatilization reaction examples…