Geologic, microstructural, and spectroscopic constraints on the origin and history of carbonado diamond
Abstract
Carbonado is a form of polycrystalline diamond found in placer deposits in
South America and Central Africa, and is one of the toughest known materials. The
source rock for carbonado is unknown, and it has unusual porosity, textural features,
and inclusion mineralogy. These have lead to a wide variety of theories on the genesis
of carbonado. The tightly bound, interlocking microtexture of diamond makes it
difficult to study, and only one previous study has been done on polished interior
sections of a carbonado.
This thesis reports the results from studying the polished surfaces of 21
carbonados from Brazil and the Central African Republic. Reflected light and
scanning electron microscopy, cathodoluminescence (CL), Photoluminescence,
Raman spectrometry, and secondary ion mass spectrometry were performed on these
carbonado samples in order to determine their microtexture and evaluate the various
theories of carbonado genesis. In addition, carbonado pore minerals and indicator
minerals from the Brazilian rivers in which carbonado is found were studied in an
attempt to gain some insight into the possible source rock for carbonado.
Some of the individual diamond microcrystals in carbonado were found to
have morphological and chemical similarities to the monocrystalline microdiamonds
found in the Dachine talc schist of French Guiana. Diamonds and chromites from the
Dachine talc schist were studied to determine the protolith of the talc schist, and to
constrain the residence history of the Dachine microdiamonds in the mantle.
Studies of florencite, a common pore mineral in carbonado, show that the Pb
that substitutes into the REE site in the florencite crystal lattice is modern, common
lead. When combined with previous geochronological studies that show at carbonado
has been associated with uranium for at least 2.5 Ga, this modern common lead shows
that the pores have been open to exchange with the exterior environment. Raman and
CL studies show that the radiation damage previously documented in carbonado is
concentrated in the areas around the pores, suggesting that they were filled with a high
concentration of uranium. One carbonado was found to host a metallic Fe-Cr
inclusions in its pores. This alloy is of a type previously reported only as
intracrystalline inclusions. These results have been interpreted as recording a three
step history for the pore mineralogy of carbonado. First, carbonado crystallized in the diamond stability field, in equilibrium with reduced metallic phases. After transport
to the surface and release from the host rock, U-bearing groundwater dissolved the
pore minerals and precipitated uranium in a redox reaction. Finally, recent tropical
weathering reoxidized the uranium, leaving recent lateritic minerals in the pores.
Because the Pb isotope model ages for carbonado (2.8-3.6 Ga) are older than
most other diamonds and much of the craton in which carbonado is found, a detrital
zircon study was performed on carbonado-bearing streams to see if any rocks of this
age or older were present in the paleo-drainage basin of the conglomerates that
contain carbonado. The detrital zircons found in carbonado-bearing streams had ages
between 3.7 and 2.1 Ga The clasts that local garimpeiros (prospectors) and
sedimentologists believe are related to carbonado had ages between 3.7 and 3.35 Ga.
This age distribution is similar to that of detrital zircons found in green Jacobina
quartzites, which were found to have the same range of ages, plus a large
concentration of 3.30 Ga grains not present in the sediments associated with
carbonado. The only possible indicator minerals found were two Cr-rich rutiles,
which may originate from metasomatized mantle. One of these Cr-rutiles was
tentatively dated using the U-Pb system as having an age of 2933 Ma. This age
corresponds with a time of tectonic quiescence in the drainage area of the carbonado
source conglomerates.
Optical, CL and Raman spectroscopic studies of polished carbonados show
that they consist of either a collection of discrete euhedral or anhedral diamond
microcrystals, or of a homogenous mix of irregular shaped grains. The ratio of these
two textural types varies between carbonado grains, but is generally constant within
each individual carbonado. Grain boundaries are generally not straight, and rarely
terminate in symmetrical triple junctions.
Raman spectroscopy shows that the level of elastic strain and compression or
tension of the diamond crystal lattice is much lower than that of diamonds formed
through shock synthesis, precipitated in chemical vapor deposition, or recovered from
ureilite meteorites. This elastic strain levels in carbonado are similar to those in
lithospheric diamonds or synthetic diamonds synthesized at static high pressures.
This suggests that carbonados were in the diamond stability field at moderately high
temperatures. SIMS measurements of carbonado using the SHRIMP ll ion probe show that
the individual crystals in carbonados have slightly different carbon isotopic
compositions and nitrogen concentrations.
There are two hypotheses that can account for the features observed in
carbonado. The first is a two stage process, whereby the euhedral grains grew first,
and the matrix diamond rapidly crystallized at a later date. The second is a
deformation process, whereby microdiamonds were concentrated and deformed to
varying degrees, resulting in the variable ratios of euhedral diamond to matrix
diamond in different carbonado stones. Because the undeformed euhedral diamonds
were found to be morphologically and chemically similar to the diamonds in the
Dachine talc schist in French Guiana, this primary diamondiferous rock was studied in
an attempt to determine how such diamond can form.
The diamonds in the Dachine talc schist were found to be type IaA-Ib. The
lack of total nitrogen aggregation means that they can not have been resident in the
mantle for more than 10 million years. The low aggregation state also constrains the
temperature of the magma that erupted them to less than about 1500 °C, as the
nitrogen in the Dachine diamond would have aggregated during transport if the
magmas were any hotter. SHRIMP carbon isotopic measurements show that these
diamonds have a range in carbon isotopic composition from typical mantle values
down to typical biogenic values. All Dachine diamonds with detectable nitrogen have
identical thermal histories, irrespective of carbon isotopic composition.
The chromites on the Dachine talc schist were a mix of metasomatized
lithospheric mantle chromites typical of kimberlites, and igneous chromites. The
igneous chromites had trace elemental compositions less depleted than those found in
boninites and komatiites, and were similar to those found in high-Mg shoshonitic
intrusive rocks. This, combined with relict volcaniclastic textures, a geologic setting
that is interpreted as an early Proterozoic arc, and the low temperatures required by the
diamonds, suggest that the Dachine talc schist may have originally been a hydrous,
arc-related volcanic rock. Such an interpretation would allow the low 813C of the
Dachine diamonds to be caused by the subduction of organic carbon.
There is still much research that must be done before carbonado diamond is
well understood. However, this theses presents several new and important constraints. The first result is that the radiation damage in carbonado was generated by the
deposition of uranium in the pores, and that both this uranium and the original pore
minerals have since been replaced by recent lateritic minerals related to tropical
weathering. The other important result is that the diamond lattice in carbonado grains
is under very little residual stress, so that whatever process that formed the carbonado
microstructures must have occurred in the diamond stability field, and not as a result
of metastable diamond growth.
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