To be simple (lack of time to elaborate, hope you can get it), fracture or microfracture in shale was made to both the source rock and to the cap rock
Why is that? Remember the bulk of the actual liquid generation from the solid
kerogen is happening largely in the shale. This appears to be where the most potential for microfracturing will occur.
Granted further catagenesis may occur in the reservoir, but not necessarily the same as in the source rock.
Why would the cap rock necessarily be subjected to the same level of overpressuring?
the source rock should be more physically flexible, and has less water content
Why are you putting these unnecessary constraints on the formations? Why would the reservoir necessarilyh ave less water? Why would the source necessarily be more physically flexible?
, the cap rock is more likely to be fractured than the source rock. If the trap is an anticline, additional mechanical factors will be added to the causes of fracturing.
Perhaps, but then not all traps are in anticlinal features, are they?
As to the feature of fluid migration along the bedding, it would be the same to both the source and the cap rocks.
Not necessarily. If the cap rock made up of clays (as in a shale) it isn't necessarily going to transmit "along the c-axis" of the crystallites (if you will). Remember a set of oriented flat plates can transmit in the plane of the plates but less so perpendicular to the plates.
In most cases, the rate of leaking of the cap rock should be higher than the rate of hydrocarbon generation.
But it
demonstrably isn't. Otherwise we wouldn't have petroleum deposits, now would we?
May be you don't like to hear this. A quick burial could indeed solve this dilemma. Of course, that would "significantly" shorten the age of the hydrocarbon.
You are now bumping up against thermodynamics and kinetics. I seem to recall quite a bit of work going on around the
Time-Temperature Index of Lopatin later expanded by Waples (I believe newer kinetic models are used, hopefully Baggins or Molal will have some info on these).
Time-temperature index (TTI).
- Complex formulation to calculate a value of TTI that is based on values for E, A, and T and t for the amount of time that organic matter stays within a 10°C window. (p. 151 Hunt)
- There is also a second relationship to calculate the value of TTI for sediment that resides for a certain time at a certain temperature
- These equations are solved for each type of kerogen (different values of E and A) and then plotted graphically to simplify their calculations (see p. 151 in Hunt, Fig. 6-3).
- The next step is to sum up all values of TTI for each 10°C window or for periods of constant temperature. This provides a value of STTI, which is related to the % oil generated by:
x% = [1-exp(-
STTI/100)]*100
- The importance of using this type of calculations is that it takes into account the kinetics of oil generation from kerogen. Because activation energy is so variable for each type of kerogen it is important to account for it.
(
SOURCE)
There's a
great deal known about the general kinetics of the reactions. You can run the reaction faster at higher temps, but you have to get them to those higher temps. The nature of the kerogen as well as the rate of heating and decomposition will help craft the final "distribution" of compounds.
Hydrocarbon generation rates are typically calculated from bulk kerogen kinetics modeled at a specific heating rate. For example, the timing of hydrocarbon generation can be illustrated by modeling the generation rate at 3.3° C/my (a reasonable worldwide average rate) from bulk kinetic data(
SOURCE)
The timing and extent of hydrocarbon generation depends on both the thermal/burial history of a source rock interval and the reaction kinetics of hydrocarbon generation from the associated kerogen.(
SOURCE)
at a given vitrinite reflectance value one kerogen may be more or less converted into hydrocarbons than second, chemically different kerogen.
...
Thus, in a given sedimentary column the oil window will vary depending on organic matter composition.(
SOURCE)
So the amount, and I believe, some of the nature of the organics you get in a certain deposit, the chemistry of the compounds reflects not only the temperature but in some ways the
rate of the reactions. We can tell something about the rates by looking at the source material and what it became and how much it produced.
Another interesting point:
Differences between old and young oils:
- a) Old oils contain more even-numbered chains than young oils (these tend to have odd number chains).
b) Old oils contain more than 50% light hydrocarbons, which are rare in young sediments.
(
SOURCE)
But further on, if you bury it quickly you will still have to heat it up to the appropriate level to reach the oil window for the given kerogen. You will then have to transmit this heat through the rock (which will take time).
How fast do you want to bury these sediments?
But a faster burial won't ease
any of the topics you are debating against in terms of getting the stuff out of the source rocks. So you bury it quickly and to the right temp, you somehow transmit the heat to the rock.
Seems then that you will have a bigger issue to explain away (another one of those pesky
mechanistic questions like came up around the water from the mantle).
Rate really does matter here, not just kinetics but also for the mechanisms proposed. How do you bury them quickly without leaving a very clear indication of extremely rapid burial?