Objections to current pegmatite theory
Last Updated: 21st May 2008
OBJECTIONS TO CURRENT PEGMATITE THEORY
OPEN VS. CLOSED SYSTEMS:
-The conduits needed to provide the fluids necessary for crystallization as well as the exit conduit needed to evacuate the pocket are not evident; no such supply openings are to be seen in miarolitic cavities, and none have been evident in virtually every pegmatite pocket I have seen and/or opened. There MUST be physical evidence of these “conduits” like brecciated & cemented zones (as proposed by Sinkankas), altered zones, fault openings, slickenslides, cuts transecting previously solidified pegmatite or granite. None of these are found in evidence, so the “outside” source of hydrothermal fluids is highly suspect.
-The source and nature of such fluid is highly suspicious as well: how is it that an “outside” source of hydrothermal fluid has the specific chemistry that is identical to the final phases of pegmatite/miarolitic growth, and not of some more general content, like just plain quartz-microcline-albite? Given that the mineral species of virtually all pockets represents both the primary granitic constituents along with species associated with pegmatite pockets like topaz, elbaite, beryl, zinnwaldite, apatite, spodumene, axinite, titanite, etc. How does this fortuitous fluid come to exist and be emplaced into the exact specific circumstances? Both the source and nature of the hydrothermal supply is highly dubious; it is FAR more likely that the source is from within the pegmatite and from confined rather than open source conditions.
-In the final consolidation phases of pegmatite crystallization and solidification, it is clear that some systems undergo rupture from increased internal pressures. Two manifestations of this phenomenon would be: 1) fracturing around the pocket zone or pocket, restricted to an area within distances corresponding to the overall effect of those conditions, and 2) overall failure of the entire pegmatite body, in which case any fluids (magmatic or otherwise) would be squeezed into any openings, fractures, or faults that transect the inner zones, where magmatic or hydrothermal fluids have not yet solidified and remain mobile. These are the so-called “replacement bodies” of Cameron, Jahns, McNair, and Page (1949). There is more than substantial evidence of this; as a matter of fact, this failure and subsequent rupture of the rock is to be found in many if not most pegmatites, and in all those that have pockets or vugs (at least to some degree). Some miarolitic cavities exhibit no rupture, while others clearly do. I only disagree with the term “explosive” as being a little overdramatic, especially since rupture and failure are far more accurate explanations from an engineering standpoint. Furthermore, a truly explosive event would most likely cause total destruction of the entire contents of a pocket, as illustrated by the use of explosives near pockets. The dissociated nature of some pocket contents can be explained by other mechanisms, especially those related to cooling and shrinkage or even phase change volume differences, which are far more likely to be the actual solution than an explosive event. I do agree that the rupture of some pockets may actually be explosive in nature, but it is clear that if this occurs, the pressure exerted is directional and away from the pocket, that is, the pressure is from within the pocket fluid and exerted on the surrounding rock away from the opening, not internally (although internal pressures are clearly at work as well).
-Dissolution is a complex set of events that cannot be easily explained by confining the mechanism to mere “solubility”. There are numerous physical and chemical forces at work here, and the process of dissolution can be very selective, despite one author’s objections to the terminology. Perhaps other descriptions for these complex processes could be adopted into etymology. It should not be dismissed because of a few select examples that only show that the process is not well understood (and therefore obviously should be studied in detail & written up).
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Recently I have been wondering just what the difference is between pegmatites and mariolitic cavities? My first thought was open vs closed as you mention, but how different are the minerals? My guess is they are the same, but perhaps a more knowledgeable person could comment. Some years ago there was a discussion on the size of mariolitic cavities. The literature suggested on the order of cm, but field collectors had been in meter sized cavities. Could pegmatite dykes just be very large mariolitic cavities?
Consider the emplacement of a large igneous intrusion. The ratio of the intrusion's surface area in contact with country rocks to the total volume of the intrusion must be quite small. This leads one to think that the hydrothermal fluids in the intrusion have had little contact with the country rocks and the component of fluid that has, makes a skarn. So what ever is in the fluids presumably has the same origin as the intrusive. Supposedly the contents of these final fluids contains all the elements that don't crystallize easily. So we get garbage can structures of Tourmaline, garnet, beryl, rare earth phospates, Niobates and Tantalates, etc. Since the fluids are close to equilibrium with the intrusive, one should also expect to find the cations of the intrusive itself in the final fluids. I thought this last point would differentiate a pegmatite in an alkaline syenite from one in granite.
The surprising number of Beryllonites from Afghanistan and Pakistan currently on the market got me thinking about this. All of these Beryllonites have the same columnar habit and look like they came from the same pocket!!! Other localities produce quite different Beryllonite habits. My first thought was: a rare mineral with the same habit must be from the same pocket or locality. Consider the rare mineral Brazilianite. It has essentially two habits, equant and prismatic, so that would argue for only two pockets, instead of the dozens of localities and thousands of pockets that do host Brazilianite. Brazillianite has only aluminum and sodium as cations, so I would suspect its occurence in an alkaline intrusive pegmatite, such as Mont St. Hilaire. But it is not there??? Why not??? Maybe I am neglecting the temperature and pressure of deposition and perhaps St Hilaire crystallised outside the stability field of Brazillianite?
Now that we have defined minerals as chemical structures, it would be nice to return mineralogy to its geological roots with an understanding of these hydrothermal solutions and how the elements get segregated in them to produce the minerals we find. I would greatly appreciate any comments that others may have.
Rob Woodside
25th May 2008 11:30pm