CA2020480C - Determining collective fluid inclusion volatiles compositions for inclusion composition mapping of earth's subsurface - Google Patents

Abstract

A collective fluid inclusions volatiles sample is released from each of a plurality of sedimentary rock samples and analyzed as it is being released to determine composition thereof. Compositions are used for mapping the earth's subsurface.

Description

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PATENT

Smith DETERMINING COLLECTIVE FLUID INCLUSION
VOLATILES COMPOSITIONS FOR INCLUSION
COMPOSITION MAPPING OF EARTHIS SUBSURFACE
FIELD OF THE INVENTION
The invention relates to interpreting subsurface structure and history by analysis of fluid inclusions in sedimentary rock samples taken from the subsurface. In 15 one aspect, the invention relates to apparatus and method releasing and/or analyzing volatiles released from myriad fluid inclusions in each of a plurality of sedimentary rock samples. Such volatiles samples released from myriad fluid inclusions in a sedimentary rock sample are referred 20 to herein as collective volatiles or collective fluid inclusion volatiles. In another aspect, the invention relates to methods of oil and gas exploration by chemical region mappin~ of the subsurface using compositlon analy-sis of collective volatiles.
SETTING OF THE INVENTION
The formation and migration of hydrocarbon in sedimentary basins are responsible for the world's petro-leum resources. Diagenetic minerals, overgrowths, and . .
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veinlets generally contain myriad inclusions smaller than 10 microns of different generations, that is, of different times of development.
Fluid inclusions in minerals are trapped por-tions of the ambient li~uid and gases present during min-eral growth or fracture healing and can be used to identify the environment in which formation occurred.
Sedimentary rock is characterized by large numbers of 10 fluid inclusions formed at different times and represent-ing different environments. The frequency of occurrence of inclusions per unit weight of sedimentary rock sample varies considerably, but, based on reasonable assumptions, is on the order of 103 to 109 inclusions per cubic centi-15 meter of sedimentary rock. It is this order of magnitude of occurrence of fluid inclusions in sedimentary rocks such as carbonates, sandstones, and shales which is referred to herein as myriad fluid inclusions. Individual rock samples may have fewer inclusions.
The systematic analysis of inclusions could pin-point areas where particular fluids such as hydrocarbons have been active and other information useful to the oil and qas explorationist. The difficult and time consumin~
methods presently available inhibit analysis of this fluid 25 record.
In view of the large numbers of inclusions pres-ent in a sample, selective individual analysis of individ-ual ~1uid inclusion data is ineffective for mapping the , . . . . .

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subsurface, though it can provide valuable information.
Succinctly stated, it is too difficult to obtain suffi-cient data by analysis of individual fluid inclusions for 5 efficient chemical mapping of the subsurface using fluid inclusion data. In addition, virtually any selection technique tends to choose certain inclusions and exclude others. Size and appearance of the inclusions themselves influence selection. Researchers may tend to select 10 larger more well formed inclusions for inVestigation, yet smaller poorly formed inclusions can contain much valuable information. Since inclusions are being formed contin-uously, ~uch selection biases results.
Prior art methods for opening more than one 15 fluid inclusion are known, such as by heating, e.g., by furnace or laser, or by crushing. Heating, however, is not effective for opening many gaseous inclusions since there are too few moles of gas present in the inclusion to develop sufficient pressure under usual heating condi-20 tions.
Crushing techniques for releasing contents ofmyriad inclusions have been such as placing rock samples in a metal sample tube, crimping the tube's ends, and crushing the tube using hammers or the like. Analysis 25 then involves opening the sample tube in a controlled environment releasing and capturing the volatiles, and analyzing for water, C02, N2, and hydrocarbon content.
Such technique is tedious and time consuming and not suit-~ ~, , - -' . , ' ' ~ ~, ' . -~,. .

able for process:ing large numbers of samples and moreover, omits to obtain composition data of great importance as will be apparent from the description of this invention.
Moreover, the described crushing technique results in biased results. The technique is not effective for observing H2S since H2S can react with the metal.
Further, the long residence time of the released gases with the surfaces freshly exposed by crushing can result 10 in adsorption changing the apparent composition of inclu-sion volatiles. A technique is needed in which volatiles are instantaneously removed from the sample and analyzed as they are being released without contact with materials which can significantly alter composition of released vol-15 atiles.
The invention relates to method and apparatusfor determ;n;ng composition of collective fluid inclusion volatiles of large numbers o~ samples of subterranean sed-imentary rocks simply, rapidly, and without need for 20 extensive sample preparation and handling compared to prior art methods.
The invention also relates to method and appara-tus for analysis of collective fluid inclusion volatiles which provide an adequate record, suitable for analysis, 25 of most all of the elements and compounds which are found in fluid inclusions.
The invention also relates to stratigraphic and~or inclusion composition mapping of the subsurface, .... . , - -:; . ~

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SUMMARY OF THE INVENTION -The invention relates broadly to a method for analyzing fluid inclusions in sedimentary rock. A plural-ity of sedimentary rock samples are placed in a plurality of sample chambers. The plurality of sample chambers con-taining rock samples are placed in an evacuable chamber.
10 The chamber is evacuated. A rock sample in a sample cham-ber is impacted e~fective for releasing a collective vola-tiles sample from myriad fluid inclusions in the rock sample. The collective volatiles sample is removed from the chamber and its composition is analyzed. A further 15 rock sample is impacted to release a collective volatiles ...... ... . .
sample. The preceding two steps are repeated until the plurality of rock samples in respective rock chambers have individually been crushed in sequence and volatiles released and composition analyzed. Then, the vacuum on 20 the evacuable chamber is released and the plurality of sample chambers are removed.
According to an aspect of the invention, the earth's subsurface is stratigraphically and interpretively mapped using composition data from statistically and stra-25 tiyraphically signi~icant numbers of collective fluidinclusion volatile samples from different locations rela-tive to the earth's surface and/or from different depths in the earth.

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According to another aspect of the invention, apparatus is provided for sequentially releasing a respec-tive collective fluid inclusion volatile sample from each 5 of a plurality of sedimentary rock samples and for deliv-ering the resulting plurality of collective volatile sam-ples to analysis means for determining composition of each sample.
The release of collective fluid inclusion vola-10 tile samples se~uentially from each of a plurality of sed-imentary rock samples occurs in an evacuated chamber which is adapted to receive, support and maintain separate each of a plurality of rock samples during release of collec-tive fluid inclusion volatiles. Means inside the chamber 15 individually impact in a timed se~uence each rock sample effective for releasing a collective volatiles sample therefrom without generally releasing the vacuum on the chamber. During times of impacting successive samples, each collective volatile sample is provided continuously 20 to analysis means for dete- ining composition.
According to an aspect of the invention, the composition of released fluid inclusion volatiles is . ~.. ..
determined using method and apparatus effective for mass spectroscopic (MS) analysis of collective fluid inclusion .
25 volatiles. According to this aspect, a series of rock samples can be ~uickly and rapidly analyzed to produce mass spectra of mass to charge ratio (m/e or MCR) responses across a range of such values encompassing abun-. :

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dant and trace inorganic and organic elements and com-pounds in inclusions which are useful in interpreting the earth's history. Thus, stratigraphically and statis-5 tically large data sets become available which are suit-able for stratigraphic mapping of subsurface structure.
According to a further aspect of the invention, the earth's subsurface is stratigraphically mapped using zones each having characteristic composition data over a 10 plurality of collective fluid inclusion volatile samples from a plurality of locations in the earth. The composi-tion data are obtained indiscriminately from all or sub-stantially all of the hydrocarbon, aqueous, gaseous, and mixed fluid inclusions present in rock samples. The 15 resulting data represent oxygen, nitrogen, argon, neon, xenon, carbon dioxide, hydrogen sulfide, ammonia, sulfate, hydrogen chloride, hydrogen sulfide, methane and other light hydrocarbons, heavier hydrocarbons such as paraffins and naphthenes, water-soluble hydrocarbons, as well as 20 other compounds occurring in analyzable quantities in aggregated released fluid inclusion volatiles.
BRIEF DESCRIPTION OF THE INVENTION
The invention will be further understood and appreciated from the following FIGURES which are described 25 here briefly and below in detail.
FIGURE 1 illustrates, in exploded view, an auto-sampler system for automated production of collective .
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fluid inclusion volatiles samples from each of a plurality of sedimentary rock samples.
FIGURE lA illustrates occurrence of inclusions 5 in a mineral thin section such as might be taken from rock sample 38 in FIGURE 1.
FIGURE 2 illustrates a cutaway view of a portion of the autosampler 10 of FIGURE 1 as assembled.
FIGURE 3A illustrates a system for mass spectro-10 scopic analysis of collective fluid inclusion volatilessamples.
FIGURE 3B illustrates, by a simplified flow dia-gram, control of the autosampler/analysis system of FIG-URE~ 1 and 3.
FIGURE 4 illustrates, by simplified flow dia-gram, a system for summing mass to charge ratio (MCR) responses for each of a plurality of scans of a range of MCR for a single collective volatiles sample to produce summed MCR values for the totality of scans for the single 20 collective volatiles sample which can be displayed as an MCR spectrogram.
FIGURE 5A schematically illustrates measurement of autosampler background data and of autosampler back-ground data plus collective fluid inclusion sample data.
FIGURE 5B illustrates distinguishing inclusion from noninclusion gases by subtracting background data from sample data.

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FIGURE 6A illustrates a logarithmic scale MCR
spectrogram of a collective fluid inclusion volatiles sample.
FIGURE 6B illustrates a linear scale MCR spec-trogram of FIGURE 6A.
FIGURE 7 illustrates a ternary plot of fluid inclusion composition data showing two zones having char-acteristic fluid inclusion compositions, each zone repres-10 enting a plurality of locations in the subsurface.
FIGURE 8 illustrates a log displaying as a func-tion of depth variations in abundance of methane in col-lective fluid inclusion volatiles in a specific well and illustrates identifying hydrocarbon migration zones and 15 seals.
FIGURE 9 illustrates a logarithmic MCR spectro-gram of a collective fluid inclusion volatiles sample in zone 150 of FIGURE 8.
FIGURE 10 illustrates a fluid inclusion composi-20 tion log displaying as a function of depth variations inabundance of argon in a specific well and illustrates identifying paleo-exposure zones.
FIGURES 11 and 12 illustrate fluid inclu~ion composition logs displaying as a function of depth vari-25 ations in C02 and illustrate at 162 and 164 respectively afluid inclusion composition region in the subsurface having wide applicability as a stratigraphic time marker.

' FIGURE 13 illustrates a fluid inclusion composi-tion log displaying as a function of depth variations in helium and illustrates another fluid inclusion composition 5 region in the subsurface having wide applicability as a stratigraphic time marker.
FIGURE 14A represents a well testing a simple fault trap.
FIGURE 14B represents a log display showing a lO fluid inclusion composition region as a function of depth characterized by paraffin abundance superimposed on the well of FIGURE 15A.
FIGURE 15A illustrates a structural contour map of a producing formation.
FIGURE 15B illustrates variations in CO2/(CO2+methane) in inclusions adjacent wells in FIGURE 15A.
FIGURE 15C illustrates ternary diagrams for wells in FIGURE 15A showing relative variation in methane, 20 CO2, and MCR41 representing heavier hydrocarbons.
FIGURE 15D illustrates variations in collective fluid inclusion volatiles compositions by displaying ter-nary plots of FIGURE 15C on a map (FIGURE 15A) of a sub-terranean ~tructure.
FIGURE 16A illustrates a ternary plot in accord-ance with the invention of C02/CH4/H2S variation in fluid inclusions volatiles in formations adjacent a well.

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FIGURE 16B illustrates a ternary plot in accord-ance with the inventions showing different characteristic populations of CO2/CH4/H2S inclusion volatiles compos-5 itions of productive and nonproductive thrusts.
FIGURE 16C illustrates a log display of H2S nor-malized relative to CO2 as a function of depth adjacent a borehole~
FIGURE 16D illustrates a log display of CO2 var-10 iation normalized relative to CH4 as a function of depthadjacent a borehole.
FIGURE 16E illustrates a log display of helium variations normalized relative to hydrogen as a function of depth adjacent a borehole.
DETAILED DESCRIPTION OF THE INVENTION
Fluid inclusions are trapped fluids occluded in the matrix of the rocks in tiny cavities which do not con-tribute to the rock's pore system, either to macroporosity or microporosity. Fluid inclusions are classified as 20 hydrocarbon inclusions when liquid hydrocarbons are pre-dominant, aqueous inclusions when liquid water is predomi-nant, and gaseous when gases are predominant. Inclusions can also be classified as liquid-filled, gas-filled, and mixed liquid-and-gas-filled inclusions are commonly 25 encountered.
The volatile components are released from fluid inclusions and aggregated, for example, by summinq during analysis data from large numbers of fluid inclusions in . , ;

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each sedimentary rock sample. The volatiles released are a heterogeneous mixture of released from all the various generations and all the various types of inclusions in 5 each rock sample. Molecules having different molecular weights move through the analysis system at different rates and require an analysis procedure which accurately and precisely reflects the original composition of the mixture. Different samples have different heterogeneous 10 mixtures of fluid inclusions depending on their respective geological histories. By analyzing composition of differ-ent heterogeneous samples in a manner effective for obtaining a record of all of the molecules present, vari-ations in composition can be identified which are indic-15 ative of differences in populations of fluid inclusions from region to region in the earth.
Referring now to FIGURE lA, FIGURE lA illus-trates inclusions such as might be observed in a mineral thin section taken from rock sample 38 in FIGURE l.
Indicated generally at 310 is a portion of a sample extracted from naturally occurring mineral growth such as might be made from a rock sample 38 in FIGURE 1.
Sample 310 consists of a cut section having a thickness of approximately 0.03-1.0 millimeter which is pol~sh~d on 25 both sides and which i5 mounted on a glass slide Inot shown in FIGURE 1). The view of FIGURE lA is a view of the polished section as seen through a microscope and is, thus, greatly enlarged. The approximate scale can be ., . ~ . .

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indicated in that substantially all of the fluid inclu-sions, like inclusion 312, formed in the various mineral growths in sample 310 are under 10 microns in diameter.
5 Sample 310 includes a plurality of mineral growths, like minerals 314, 316, 318, 320, 322, and 324. Minerals 316 and 318 each include a mineral overgrowth 326 and 328, which acts as and is referred to as a cement.
Mineral 324 includes therein a plurality of pri-10 mary inclusions, like inclusions 330 and 332. These inclusions were formed during the initial growth of min-eral 324. A healed crack 334 is formed in mineral 324, and a healed crack 336 is formed in mineral 322 and in mineral 324. Crack 334 was formed in mineral 324 after 15 the original growth of mineral 324, and thus after the primary inclusions, like inclusions 330 and 332 were formed. Crack 336 was also formed in minerals 322 and 324 after the formation of the primary inclusions in both min-erals 322 and 324. Each of cracks 334 and 336 have a plu-20 rality of secondary inclusions, as shown, formedtherealong. These secondary inclusions were formed during healing of cracks 334 and 336 when mineral growth devel-oped in the cracks. It is to be appreciated that the sec-ondary inclusions in crack 334 trap environmental fluids 25 at a later time than the primary inclusions in mineral 324 and the secondary inclusions along crack 336 trap such fields at a later time than when the environmental fluids were trapped in the primary inclusions in both ; ~, ~ ...................... .

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minerals 3~2 and 32~. ~oreover, the secondary inclusions in crack 33-~ may well be formed at a time far removed from those formed in crac~ 336, and thus, the secondary inclu-5 s:ions in crack 334 may be of a different generation thanthose along crack 336. Likewise, the primary inclusions formed in the various minerals and cements in sample 310 may be formed at vastly different items from one another, thus trapping the environmental fluids present at the time 10 of formation.
In accordance with the .invention, -these various classes and generations of fluid inclusions are indiscri-minately opened and fluid inclusions released. Prefera-bly, all or substantially all or at least a preponderance 15 of the fluid inclusions are opened and volatiles released.
A sample contains typically only a fraction of a gram and, since inclusions are formed on an ongoing basis, represents an integration of the buri~l history over time which may, however, differ considerably from another 20 sample just a few inches away.
Each sample is best compared to many other sam-ples to obtain information reliable for hydrocarbon explo-ration. Thus, each fluid inclusion compos'ition region has a characteristic fluid inclusion composition over a plu-25 rality of locations in the earth. Comparison of only afew samples leaves too much uncertainty regarding whether or not individual observations are typical of the forma-tion. Referenc~ to FI~RES 7, 8, and 9 below show that "
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there is significant scatter in the data and therefore, that large numbers of samples are required to reliably identify trends. For FIGURES 7, 8, 9, the rate of sampl-5 ing the subsurface is about every 6Q-90 ft. From 50-10,000 or more samples are analyzed for each strati-qraphic investigation, preferably 100 to 500 or more to obtain statistically and stratigraphically reliable data sets. Samples are preferably taken at least every 200 ft, 10 lO0 ft, 50 ft or less. Sixty-foot spacing has provided excellent results in many runs. More frequent sampling can also be advantageous. Referring again to FIGURES 7, 8, 10, it will be appreciated that each zone represents a plurality of samples:

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Zone Fiqure of Samples Generally, experience indicates that zones can be reliably determined when each ~one is characterized by 25 at least 5 samples, and of course, more samples improve reliability and fewer samples can also be used in cases where data scatter permits.

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Collective fluid inclusion volatile composition data can be inspected for trends across a domain being stratigraphically mapped. For stratigraphic mapping, the 5 samples are selected to span a domain in a sedimentary basin. Each well in the domain can then be examined as described in the preceding paragraph and the results can be displayed across the domain or even a particular forma-tion in the domain.
The samples can be washed drill cuttings, cores, outcrop samples, soil samples, and the like. Drill cut-tings are widely available and allow investigation of sub-stantially the entire length of a borehole. Further, drill cuttings have been archived from many existing wells 15 so that new wells or samples are often not needed. A rock sample of about 10 cubic centimeters or even less permits numerous runs, if desired, since only a portion of a cubic centimeter is needed for each run.
For domain studies, multiple spaced apart wells 20 can be sampled along substantially the entire depth or along a zone of particular interest, for example, a par-ticular formation, in several wells. These domains of analysis are in sedimentary basins and provide lnformation about geological formations ad~acent each of the wells 25 surveyed in an area. S0 to 100 or more samples spanning a domain or interest are selected and analyzed to determine fluid inclusion composition.

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According to the lnvention, the collective vola-tiles are preferably obtained by impacting each rock sample, as described below in detail, since this releases 5 both liquid and gaseous inclusion contents. Other tech-niques can also be used, for example, heating, for example using a heating robe on one of rams 50 described below or by laser. Due to the relatively small number of moles of gas present, such techniques are generally ineffective for 10 opening gaseous inclusions, although they work well for liquid-filled inclusions. Heating also may cause non-inclusion gases to be evolved.
Referring now to FIGURE 1, FIGURE l illustrates in exploded view a system including a controller for 15 releasing, delivering and analyzing composition of a plu-rality of fluid inclusion volatiles sample. The apparatus comprises releasing means 10 for sequentially and individ-ually impacting and deforming each of a plurality of sedi-mentary rock samples effective for releasing a collective 20 fluid inclusion volatiles sample from each analytical means 12 for determining composition of each fluid inclu-sion volatiles sample as it is being released, delivery means ll, 27, 28 for delivering each fluid inclusion vola-tiles sample from releasing means to analytical means as 25 it is being released, and controller means 16 for causing a collective fluid inclusion volatiles sample to be sequentially and individually released by the releasing means 10 and for causing each collective fluid inclusion .. :

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volatiles sample to be sequentially and individually ana-lyzed by the analytical means 12 as it is being released.
FIGURE 1 illustrates an autosampler 10 con-5 trolled by controller 16 and providing collective fluidinclusion volatiles samples for each of a plurality of rock samples to mass spectrometer 12. A vacuum pump 14 places vacuum stage 10 under a vacuum at the start of a sequence of analyses. Thereafter, the system is main-10 tained under vacuum by pumps 15' associated with the massspectroscopic system. See FIGURE 3A.
System 10 includes upper housing 27 and lower housing 28 having seal 30 therebetween for forming evacua-ble chamber 60 (see FIGURE 2) when housings 27 and 28 are 15 aligned and joined. Seal 30 can be an oxygen-free high conductivity copper gasket. Housings 27 and 28 can be adapted with knife edges for sealing by engaging gasket 30. A new gasket can be used for each run. The evacuable chamber has an outlet 11 with valve llv and 20 functions for delivering released volatiles to analysis as they are being released.
Upper housing 27 has a plurality of linear vacuum feedthrouqhs 19, 21, 23, and 25 for permitting shafts from pneumatic rams 1~, 20, and 22 and motor 24 to 25 pass into chamber 60 (see FIGURE 2) without loss of vacuum. Each of rams 18, 20, 22, and motor 24 have a housing with a flange 18f, 20f, 22f, 25f, respectively, for sealingly mating with flanges l9f, 21f, 22f, and 25f S

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of the linear feedt}lroughs. Motor 24 can be a stepper motor or a servo motor with a shaft encoder or any motor capable of having the shaft position controlled. Control-5 ler 16 can include systems as are well known for generat-ing drive signals for motor 24 and for generating signals and driving forces for driving rams 18, 20, 22.
Lower housing 28 comprises flange 28f, sidewall 28s, and base 28b. Base 28b has a groove 32 10 therein in which a plurality of bearings 34 can be placed.
Circular carousel 26 is adapted with a plurality of sample chambers 36 therein and centered slot 46 for engagably receiving shaft key 44 on stepper motor shaft 42. Car-ousel 26 has groove 32b for engaging bearings 34 in 15 groove 32a in base 28b. As a result, when carousel 26 is placed in lower housing 28, grooves 32b and 32a cooperate to align the carousel 26, and bearings 34 provide for rotation of carousel 26 in response to motor 24 turning shaft 42 having key 44 engagably connected with slot 46.
Sample chambers 36 are each effective for receiving a rock sample 38 and for maintaining it in a confined space during volatiles release between the walls and base of the chamber and the impacting means.
As illustrated, there are three pneumatic 25 rams 18, 20, and 22 passing through upper housing 27.
More or fewer rams can be used. Illustrated carousel 26 has three concentric rings of sample chambers 36, and each pneumatic ram aligns with a re.spective concentric ring of .
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sample chambers. Ram 19 is illustrated with plunger 52 and ram tip 54. Ram 19 aligns with outer ring 360; ram 20 aligns with intermediate ring 36i, and ram 22 aligns with 5 central ring 36c. Thus, when a sample chamber 36 is aligned with a respective ram, the ram can be actuated to impact a sample 38 in the chamber effective for releasing a collective volatiles sample. Preferably, each sample chamber is also provided with a sample chamber slug 40 to 10 prevent cross contamination of samples during impacting.
Slug 40 can be considered part of the impacting means.
Sample 38 and slug 40 are shown enlarged in circle 39 for clarity. However, slug 40 is adapted to cover sample 38 in chamber 36 while permitting volatiles to escape through 15 an annulus between slug 40 and the wall of chamber 36.
While only one slug 40 and sample 38 are shown, there will usually be as many slugs 40 and samples 38 as chambers 36.
Referring now to FIGURE 2, FIGURE 2 illustrates in greater detail the operation of the pneumatic rams.
20 Illustrated in FIGURE 2 is pneumatic ram 19 which as indi-cated is aligned with the outer row 360 of sample chambers on carousel 26. In response to a signal from controller 16 (see FIGURE 1), the pneumatlc ram bellows 48 expand, driving shaft 50 and plunger 52 into contact with 25 the slug 40, impacting sample 38 (see FIGURE l) in chamber 36. Impacting of the sample may occur one or more times, preferably multiple times under control of control-ler 16 to ensure release of substantially all fluid inclu-- '~

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sion volatiles. The released fluid inclusion gases then are transported within chamber 60 through a space between the lower surface of upper housing 27 and the upper sur-5 face of the carousel 26 to mass spectrometer 12 for analy-sis .
Impacting of the sample preferably occurs while the sample is closely confined by a slug 40 in a chamber 36. The impact can be any impact sufficient for 10 releasing a collective fluid inclusions volatile sample, for example, by crushing, pulverization, and the like.
Preferably, the impact is effective for causing a deforma-tion or concussion of the sample effective for releasing a collective volatiles sample substantially without crumbl-15 ing or powdering the sample. For most drill cuttings run,an impact of about 400 pounds per square inch is effec-tive. In this way, creation of new surfaces on which adsorption of released volatiles can occur is ;ni ; zed.
The result of crushing is preferably a rock sample 20 deformed and shaped by the sample chamber and the crushing means into a compacted aggregated mass.
Impacting can take place virtually instantane-ously up to about 10 seconds or even longer. Ten seconds has provided highly satisfactory results. In such case, 25 the plunger impacts the rock sample and maintains deform-ing fluid inclusion pressure thereon for 10 seconds, for example. When iteratiVe impactin0 is employed, all of the iterations can be made to occur in 10 seconds or less if . , .. ,, . ~ , ,- ~
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desired. Impacting can be for a time effective for releasing a volume of fluid inclusion gasses. Release of substantially all, or at least a preponderance of, fluid 5 inclusion volatiles is preferred.
As illustrated, the invention includes a con-troller 16 for controlling sampler 10, for example, by controlling motor 24, rams 18, 20, 22, to release seguen-tially in bulk from each of a plurality of rock samples 10 fluid inclusion components and for controlling mass spec-trometer 12 for removing and analyzing the released fluids.
Controller 16 is described in more detail in reference to FIGURE 3B.
Controller 16 can be, for example, a personal computer programmed for controlling the autosampler and for storing composition data produced from mass spectrome-ter 12 on disk together with apparatus for driving the rams, motor, controlling mass spectrometers and the like.
20 Such equipment is well known and can readily be assembled by those skilled in the art for the invention. Use of a personal computer for such control is described herein but any suitable controller can be used.
As indicated at 220 in FIGU~E 3B, certain pre-25 liminary operations can be controlled by controller 16.Thus, controller 16 can generate signals for formatting a data disk in controller 16, for calibrating mass spectrom-: ~ - ,,: : , : .:
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eter system 1~, and for positioning carousel 26 for analy-sis of a predetermined first rock sample.
For each rock sample, controller 16 generates 5 signals causing measurements and recording of background data, causing a rock sample to be impacted, causing meas-urement and recording of background plus fluid inclusion volatiles, causing storing of preliminary recorded data on disk and querying whether all samples have been run. If 10 all samples have not been run, controller 12 generates a signal controlling motor 24 for causing carousel 26 to position for crushing of the next rock sample. When all samples have been run, controller 12 can perform end of run procedures such as releasing the vacuum on the system, 15 data transfer, and the like. The operation of controller 16 is illustrated in more detail in FIGURE 3B
discussed below.

Rock Sam~les Washed cuttings, core, outcrop samples, even soil samples collected at various locations in or on the earth, can be analyzed. Percussion sidewall cores are currently not preferred due to grain fracturing, resulting in inclusion breakage, during coring. As discussed in reference to FIGURES 5A and SB below, the invented method discriminates inclusion from noninclusion gases, and fre-quently it does not matter if cuttings are from a well drilled with oil or from one drilled with water based ,~

-: . -' - ' ' ' ~ ' ' ~ ' ~' ,, :, muds. Sometimes, however, the background levels given off by some cuttings from wells drilled using oil based muds is so high as to mask response from opening the inclu-5 s:ions. Drilling and other fluids present in the pores oradsorbed on the rock, such as formation fluids occurring in the rock's pore system, may be removed before release of fluid inclusions to reduce background levels.
Extraction of drilling mud residues in solvent appears to 10 eliminate the problem, but is rather expensive and may take weeks or months ~or the several hundred samples that may be used in a single inclusion study. However, the preferred technique for opening the inclusions, described below, discriminates inclusion from noninclusion gases in 15 most cases. Further, heating for example at 200~C in air overnight prior to analyses often reduces background to acceptable levels.
The technique can be used on carbonates, clas-tics, and sandstones.
A typical rock sample is less than 10 cc (cubic centimeters) in volume which provides sufficient material for several runs, if necessary. Core and outcrop samples are usually broken prior to analysis while drill cutting samples can be poured directly into the sample holes.
25 Individual samples for analysis generally range from about 1/100 to about 1/2 cc, typically about 1/25 to about 1/2 cc.

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For single well profiles, a cuttings sample for every 60 to 90 ft can be analyzed. More frequent sampling can be used across zones of particular importance. The 5 samples are preferably not composited, that is, drill cut-tings from different footages are not combined although composited samples can be used if desired. The freguency of core and outcrop samples, for example every 10-20 ft, depends on the scale of the problem being addressed and 10 the availability of material. Broadly intervals between 1 and 200 ft are preferred.

Analyses Samples are analyzed using the fluid inclusion autosampler. Samples 38 are loaded into carousel 26 con-taining sample holes 36. Steel slugs 40 are placed in holes 36 on top of the samples. During analysis, slugs 40 are rammed by plungers 50 having ram tips 52. Slugs 40 ensure the entire sample is impacted and prevent intersam-ple contamination from scattered bits and pieces. Depths are recorded by entry into a computer such as controller l~ as the samples are loaded into predetermined sample chambers in the carousels. The depths can later be transferred to another computer such as a mainframe for analysis of resultin~ data if desired.
The loaded carousel 36 can be heated at 200~
overnight prior to analyses to drive off most of the absorbed water and other volatiles, reducing pump down , .: , ~, , , ~ L S' :3 time in the vacuum system. Loaded carousels 36 can then be removed from the drying oven and loaded into lower housing 28. In pumpdown configuration value 13v is open 5 and value llv is closed; in automated sampling configura-tion, llv is closed and 13v is open. Autosampler 10 can be heated to maintain the samples at about 150~C during operation. Inlet and outlet lines to mass spectrometer system 12 can also be heated to about 150~C.
Generally, the analysis temperature can be any temperature effective for volatilizing particular mole-cules of interest up to a temperature less than that at which thermal decrepitation causes release of fluid inclu-sion volatiLes. For oil and gas exploration, temperatures 15 in the range of about 150~ to about 200~C are particularly advantageous for volatilizing of hydrocarbons.
Autosampler 10 is then evacuated, for example, first to very high vacuum using a turbomolecular pump such as pump 14 not open to the mass spectrometers. The entire 20 system can then pump down in its analytical configuration, for example, for a period of time, for example, three hours before the analytical session is begun. When the system is in analytical configuration, released inclusion volatiles from autosampler 10 can be pumped directly 25 through mass spectrometers 14 (See FIGURE 3A). That is, gas evolved during analyses must be pumped through the ionization chambers of the mass spectrometers in order to .. ..
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be pumped awa~. This can be seen more clearly in FXGURE 3A.
The system is maintained at a vacuum of about 5 10 8 to about 10 6 torr. Even during release of vola-t:iles, the pressure will not decrease much below 10 6 torr. Generally, the pumps evacuating the system during analytical configuration maintain low pressures to insure substantially all of released volatiles or passed 10 through mass spectrometers for analysis.
Autosampler 10 is depicted in FIGURES 1 and 2.
A circular groove 32 in the base of carousel 36 rests on ball bearings 34 that rest in a circular groove in the bottom plate of lower housing 28. Asymmetric tab 44 fits 15 into the notch 46 in the carousel. Asymmetry of the tab and notch assure that the sample tray is correctly posi-tioned in the autosampler so that each sample has a uniquely determined position relative to the sampler.
Upper and lower housings 27 and 28 of autosampler 10 are 20 fastened together. Oxygen-free high-conductivity copper gas~et 30 is inserted between the two halves prior to con-necting them. Vacuum seal is made by steel knife edges in both the upper and lower halves cutting into the gasket.
Preferably, no hydrocarbon components are used anywhere in 25 the system.
Motor 24 under control of controller 16 via line 12c drives the shaft 42 that turns the asymmetric notch 44 that turns carousel 36. As illustrated, there .
, , are three impact assemblles, orle for each of the three sample rows. Each sample, in turn, is placed under one of the impactors.
FIGURE 2 shows a cut away view of impactors positioned over a sample with autosampler lO sealed. The impactor can be a stainless steel bellows 48, which trans-mits linear motion generated outside the vacuum chamber to shaft 50 inside the vacuum chamber G0. Bellows 48 can be 10 driven ~rom above by an air piston which can be included in controller 16 for both lowering and raising belows 48.
Ramming tip 52 covers the end of shaft 50. Shaft 50 is positioned directly overhead of slug 40 that rests on top of rock chips 38, as shown in FIGURE 1. The sample is now 15 ready to be analyzed.
FIGURE 3A illustrates mass spectrometic analysis of collective fluid inclusion samples in accordance with the invention.
Referring now to FIGIJRE 3A, there is illustrated 20 a source 10' of collective fluid inclusion volatiles sam-ples, such as autosamplar 10 in FIGURE l, connected via line 11' having valve ll'v to a preferred arrangement of mass spectrometers 12'. During analytical config~lration, valve ll'v is open and samples are being withdrawn as they 25 are released by crushing. Thus, the system depicted in 3A
is dynamic, i.e., open to the sampler 10' during sample release. As illustrated, the mass spectrometers are arranged in two banks of three, each bank having a 3 ~

pump 15' for drawing sample from line 11' through each of mass spectrometers 12' via outlet line 13'. Each mass spectrometer is configured to sample a specific set of MCR
5 r~esponses using the optimum gain for each, for example, as follows:

Mass to Change Ratio Mass SPectrometer Responses Sam~led 1 2,16,17,18,28,~4 2 3,4,12,13,14,15,19-27,29-43,45-60 There are generally no peaks at MCR 5 to 11. Those skilled in the use of MS will appreciate that by assigning specific MS to samples, a set of MCR responses which have comparable amplitudes, time lost in switching amplifiers for the MS can be minimized. Thus, MSl samples the most abundant MCR < 61 and MS2 samples the least abundant MCR ~ 61.
The 0-lOv signal outline of each mass spectrome-ter 12' is operably connected to a bank of five signal conditioners 17', each configured for a different optimum gain, for example, as follows:

25 Sianal Conditioner Gain Confiauration O-lOv 2 0-5v 3 0-lv 4 0-0.5v o-o.lv ..

2~0 The outputs of signal conditioners 17 are pro-vided to analog to digital converter (ADC) 17' and then to computer controller 16'. For simplicity, only the output 5 of one MS 12' is illustrated but the other MS 12' are also so configured.
As indicated, the MS system of FIGURE 3A is open to sampler 10' during sampling. This minimizes residence time of volatiles in the sampler 10' but means that vola-10 tiles are being passed through the MS system over a periodof time dependent on the relative molecular weight of the volatiles and the period of time when volatiles are being released from a particular sample. For example, the rate of travel of volatiles is molecular weight dependent so 15 that lighter volatiles are analyzed before heavier vola-tiles. Also, where sampler 10' is an autosampler 10 according to another aspect of the invention, impacting the sample to release volatiles takes a discrete amount of time and if multiple impacts are used, there can be a 20 series of releases of volatiles for analysis of a single rock sample.
According to aspects of the invention, it is desirable to have a record of MCR ~or a rock sample which reliably permits comparison of compounds represented by 25 one or more MCR to one or more others.
According to an aspect of the invention, there is provided an MS system for producing such a reliable record. The MS system is configured and controlled for .
: . .

scan~ing a range of MCR of interest a multiplicity of times during the period of release of volatiles from each rock sample, and the results from all the multiplicity of 5 scans are summed on an MCR by MCR basis for each rock sample.
As described herein, the MCR range of interest is from about 2-300 MCR to encompass an advantageous range for analysis. Greater or lesser ranges can also be used.
10 As indicated, the MS system is configured to sample the most abundant MCR using a single MS to avoid lost time due to amplifier switching. As described herein, the multi-plicity of scans is 256. More or fewer scans can be used.
However, reduction in number of scans leads to loss of 15 precision and accuracy. Hence, more rather than fewer scans are desirable.
Referring now to FIGURE 3B, FIGURE 3B illus-trates control of the MS system of FIGURE 3A integrated with control of the autosampler 10 of FIGURE 1. Gener-20 ally, the system scans a sampler 10', a multiplicity oftimes during a time when no sample is being released and sums the results on an MCR by MCR basis. The system then scans a sampler 10' a multiplicity of times during a time when a collective volatile sample is being released from a 25 particular rock sample and sums the results on an MCR by MCR basis. The system repeats the preceding two steps until a plurality of samples has been run. In a prelimi-nary data reduction step, background readings taken before ,, : - , ~

:, .

~ Q~

each sample ls read can be removed from the sample read-ings. The preliminary data reduction is described in more detail in reference to FIGURES 5A and 5B.
Referring now to FIGURE 3B in detail, FIGURE 3B
illustrates a system for control of sampler 10 and the MS
system of FIGURE 3A using a personal computer in which data are stored on disk and later transferred to another computer for analysis. Clearly, other controller systems 10 for use with the invention are also available and the invention is not limited to the particular computing hard-ware described.
Step 220 is for performing certain preliminary operations such as formatting a data disk, calibrating the 15 MS, and positioning carousel 26 for crushing of the first sample.
Step 222 is ~or setting the beginning of the MCR
range (MCR = 2). Step 224 is for controller 16 sampling the output of the MS configured for MCR2 and step 226 is 20 for the computer selecting a signal conditioner for opti-mum gain for MCR 2 signal and causing the selected condi-tioner output to appear on the output line of ADC 17' where the computer samples it (step 228). Step 230 is for sending the MS to the next MCR to be tested. This can be 25 accomplished, for example, using a digital to analog con-vertor in controller 16. See Table supra for a particular assignment of MCR to mass spectrometers. Step 232 is for storing the sampled ADC in the appropriate summer. The ,, .

. ;: .
: ~ ~. ' ' .'.' ' ~ . . .

computer then by Steps 234 and 236 are for the computer sampling in the same way via loop 244, the MS assigned to the next MCR until the full range of MCR, as illustrated, 5 MCR 2~300 has been scanned.
The step for sending the appropriate MS to the next MCR is illustrated in FIGURE 3A by line 121 and in FIGURE 3B by step 230. It can be accomplished using con-troller 16 including a DAC (digital to analog converter).
10 Thus, a personal computer can provide a signal selecting the next MS for the next MCR to a DAC for a particular mass spectrometer. The DAC can then cause the appropriate mass spectrometer to be configured for the next MCR to be read.
By step 238, the full range of MCR of interest is scanned a multiplicity of times for each rock sample, the data for each MCR being summed on an MCR by MCR basis for the multiplicity of scans. After 256 scans, the com-puter tests whether there was a scan of background data or 20 of sample data by step 240. This can be as simple as deteL ining the set of 256 scans as the second set since impacting the previous rock sample. Upon determining that the readings were of background data, step 242 stores the background data for the sampler in the computer 19 memory 25 and generates a signal to autosampler 10 causing the first sample to be impacted and returns to step 244.
Steps 224 through 240 are then repeated and when step 240 now responds indicating that sample data have . : . .
.

.

been measured, step 246 stores the sample data on disk.
Step 248 inquires whether all samples have been run and if not, by step 250 and loop 252 provides a signal via 5 line 12c (see FIGURR l) to sampler 10 to position the next rock sample for analysis. After step 248 indicates that all samples have been run, step 254 ends the run, and the data can then be transferred (see step 256) to another computer for preliminary data reduction. All of the steps 10 described above can be readily implemented by those skilled in the art of computerized control from the description herein using commercially available equipment.
Referring now to FIGURE 4, an autoranging rou-tine is shown for selecting an optimum signal conditioner 15 for each MCR reading and for summing the readings on an MCR by MCR basis. For each MCR reading, a particular signal conditioner is selected by, for example, 0-5v gain control 200. Then each MCR response is directed to the appropriate memory for summing by steps 202, 204, 206, 20 208. Thus, if step 202 indicates that the signal s for the particular MCR is ~5v, the response is sampled on the 0-lOv channel and summed using the 0-lOv summer 203. If l<s<5, step 204 samples and sums the response using the 0-5v summer 205. If 0.5<s~1, step 206 samples and sums 25 the response usin~ the 0-lv summer 207. If O.l<s<0.5, step 208 samples and sums the response using the summer 209; if <0.1, using the summer 211. After, for example, 256 mass scans are summed for each mass response ~ . .

.
.: :
~ ~
:.
~ : .

in the range of 2-300 mass to charge ratio ~mits, computer 16 can sum, the MCR responses for each MCR over all scans and can generate for each collective fluid 5 inclusion volatiles sample a mass spectrogram such as the one shown at 220 in FIGURE 4B. Mass spectrograms for autosampler background data and for a sample are also illustrated in a simplified manner at 132 and 136, respec-tively, in FIGURES 5A and 5B.
During operation, controller 16 reads the output of mass spectrometers 12' 256 times in about 10 seconds as a volatiles sample is being released from an individual rock sample to collect 256 complete MCR spectra from MCR 2 through 300, i.e., for each volatiles sample 256 scans of 15 MCR 2-300 are made. A summer 213, for example, in com-puter 16, sums the 256 responses from each MCR from all of the multiplicity of scans as they are collected. A
0-10 volt signal from each mass spectrometer is sent to a bank of five signal conditioners set at different gains.
20 The gains of the 30 signal conditioners are calibrated using a National Bureau of Standard standard. The com-puter uses an autoranging routine such as shown in FIGURE 4 to select the optimum signal conditioner for each MCR scan. For each MCR, after selecting the optimum 25 signal conditioner, collecting the data, adding it to the total for that MCR, and storing the result in memory, con-troller 16 triggers the appropriate mass spectrometer system to proceed to the next MCR. The computer then ...
,' '~

~~ h reads a signal from the mass spectrometers configured to sample that MCR, and so on until 256 MCR scans are summed.
There is about 100 microseconds between each MCR sampled.
A plurality of mass spectrometers is used to sample a range of MCR's of interest in oil and gas explo-ration. Preferably, substantially all or at least a pre-ponderance of ranges such as 2-60, 2-120, 2-180, 2-240, 2-300 and the like are scanned a multiplicity of times as 10 a volatiles sample is released from each rock sample.
For each rock sample the summed data from the first multiplicity of scans are an analysis of the back-ground gases in the system (see 130 in FIGURE 5A). These gases result from the breakdown of hydrous minerals as 15 well as the release of volatiles adsorbed on the rocks as well as residual gases remaining behind from previous sam-ples. All rock samples as well as the autosampler and the rest of the vacuum system contribute to the system back-ground.
Once the background is characterized, the com-puter signals and controls the appropriate air piston one or more times to ram the appropriate steel slug thus impacting the sample (time of occurrence illustrated in FIGURE 5A by arrow 134). 256 new scans of 2-300MCR are 25 initiated each time the rock sample is impacted or while the rock sample is crushed multip~e times. Most of the fluid inclusions in the sample are broken by this process and release their gas into the vacuum system. The sum of - . . - . . - .
. , ~ ~. , ~ , ' .
: . : .~ . . : :
!~ :

the second and subsequeIIt multiplicity of 256 scans is the analysis of the fluid inclusion gases plus the background, as illustrated by reference numeral 136 in FIGURE 5A.
Referring now to FIGURE 5B, FIGURE 5B illus-trates a pre]iminary data reduction step in which the background gas contribution 132, characterized immediately before impacting each rock sample, is subtracted from data 136 on an MCR by MCR basis for each collective fluid 10 inclusion volatiles sample plus background. This tech-nique is effective for discriminating inclusion from non-inclusion gases so that the final volatiles record is representative of inclusion gases.
This is a gas analysis; there is no carrier 15 fluid. The analyses of each sample take about 25 seconds.
A short period of time, for example, ninety seconds, can be allowed between samples for the system to pump away as much of the released inclusion gases as is practical.
Many substances which are liquids at room temperature and 20 pressures are gases under ultra high vacuum and 150~C, such as water and gasoline range hydrocarbons. Very long chain hydrocarbons, however, remain liquids even under these conditions, and therefore, are typically not ana-lyzed.

Mass S~ectrometrY

The composition data used for stratigraphic map-ping of subsurface structure are preferably the results of : . ~ . ; , .
,. , :~ ;

: , - . , , :

Q~

mass spectrographic analyses of the volatile contents of fluid inclusions released in bulk from rock samples.
Apparatus and techniques for quickly and efficiently pro-5 ducing samples of bulk volatiles are described above.
In the mass spectrometer, the molecules in each bulk sample are ionized, accelerated, separated according to MCR, and measured. Ionization i9 usually accompanied by partial fragmentation of the molecules which is charac-10 teristic of specific molecules and operating conditions.While fragmentation complicates interpretation - a given molecular weight fragment can be derived from different molecules - it also permits distinguishing between isomers and gives molecular structural information. The output 15 can be various forms of MCR versus abundance records, mass spectrograms, and the like.
Although mass spectrometry is preferred, other techniques, for example, chromatographic (GC), a gas chromatographic/mass spectrometry analysis GC/MS can be 20 used.
Compared to MS, GC and GC/MS analysis are rela-tively slow, requiring as much as an hour per sample. MS
analyses take~ only 24 seconds per sample, with ninety seconds of self-imposed pumpdown between samples. Strati-25 graphically and statistically large data sets are neces-sary using fluid inclusions to aid in locating subtle traps having reservoired hydrocarbons and to map hydrocar-bon migration pathways and barriers.

.
;;

i3 Mass spectrometry analyses many gases not ana-lyzed by GC and GC~MS. In particular, gases diagnostic of paleo subaerial exposure zones, such as ~2~ N2, Ar, Ne, 5 and Xe are not analyzed by these other techniques. Yet, this information may be critical in subsurface correlation and burial history reconstructions. Other gases not typi-cally analyzed with GC and GC/MS include CO2 and H2O, the two most abundant gases in fluid inclusions. Ammonia, 10 sulfate, HCl (a possible salinity indicator), methane and other light h~drocarbons, and H2S are usually not ana-lyzed. In some reservoirs, the only constituents of note are methane, CO2, and H2S. H2S has been found to be a useful indicator of thrust faults in some basins and a 15 stratigraphic correlation marker in others.
Aqueous inclusions may contain water soluble hydrocarbons that may be oil proximity indicators. These inclusions would not be considered if fluid inclusion investigations were restricted to samples having large 20 abundant oil inclusions.
MS also discriminates between noninclusion and inclusion derived gases. Such discrimination is not pos-sible using GC or GC/MS. Fluid inclusion samples analyzed using theso other techniques must be virtually absolutely 25 clean in order to avoid analysis of cont~ ln~nts, requir-ing much more sample preparation.
One reason why fluid inclusion efforts have pre-viously failed to provide significant and widespread bene-.
:...... .. . . .
:, :

~: :, ~ :

fit to exploration is because these efforts were often based on techniques, such as GC/MS and Laser-UV fluores-cence microscopy, that are applicable only to small num-5 bers of samples and are only useful for those sampleshaving large and abundant oil inclusions. All samples contain fluid inclusions that can be analyzed using mass spectrometry, and the stratigraphic analyses of fluid inclusion mass spectra has provided useful information, 10 regardless of the presence of ab~mdant oil inclusions.
The mass values of some fragments encountered in fluid inclusion analysis and source molecules are shown in the following table.

MCR Siqnatures - Inor~anic Fluid Inclusion Gases Table 1 Inorqanic Gases MCR Si~nature He 4 C02 22,44 Ar 40 Nz 28,14 HzS 34 ~2 32 S0(1-3) 48 CoS 60 Ne 20,22 HCl 35,36,37,38 Xe129,130,131,132,134,136 .

~ Si ~

--gl -Mass Siqnatures - Oraanic Fluid Inclusion Gases Table 2 Orqanic GasesMass Sianature Methane 15 Ethane 30 Propane 44 Butane 58 Benzene 78 Toluene 91 Xylene 105 Triterpenes 191 Steranes 217 The mass spectra for the higher mass organic compounds becomes very complicated with many overlapping mass spectra peaks, m~k;ng it difficult or impossible to identify single compounds with certainty. Classes of 15 organic compounds, however, share common fragments:

MCR Siqnatures - Hiaher Mass Oraanic Com~ounds Table 3 Oraanic Gases MCR Siqnature paraffins 57 naphthenes 55 aromatics 77 toluene 91 alkylated naphthenes 97 In addition to these peaks, these hydrocarbon families tend to give responses at every 14 mass numbers due to the CH2 repeat in organic polymers:

;, - . , . . , ~ . .
~: - ~ . . : : , : ................................. -: ~ .. , ., , . : , - . : :

MCR Si~natures - Hiaher Mass Orqanic ComPounds With Repeatin~ CH2 Table 4 Or~anic GasesMCR Siqnatures paraffins57,71,85,99,113,127, etc.
naphthenes55,69,83,97,111,125, etc.

In the higher mass organic compounds, quantitative ana-lyses of individual compounds are not as important as 10 identifying characteristic regions or zones of fluid inclusion composition (fingerprinting the regions) using fluid inclusion composition data. Such identification of regions in the subsurface re~uires a plurality of samples from a respective plurality of locations in the earth for 15 characterizing each region. Once a class of inclusions is fingerprinted, its distribution in the earth can be mapped.
Referring now to FIGURE 6, FIGURE 6 illustrates results of analysis of a sample after autosampler back-20 ground has been removed. FIGURE 6 shows a mass spectrumfor a collective sample to be composed of a multitude of peaks at various MCR peaks. This is not only the result of there being a large number of compounds in the inclu-sions, but also because compounds dissociate or "crack"
25 during ionization by electron bombardment in the mass spectrometer. For instance, the molecular weight of water, H2O, is 18. However, water has a characteristic cracking pattern resulting in contributions on masses 17 - . .
.
. .. . . . : .
., - . : .:
- ~ .
.'' . ~ ' , ~3~ 3 (OH~, 16 (O), and 2 (H2). C02 has its main contribution on mass 44, but also llas major contributions on 28 (CO), 16 (O), and 12 (C) as well as 22 (C02++). Methane, CH4, 5 has a molecular weight of 16, and methane's main peak is on 16, but water and C02 also have major O contributions on 16. ~herefore, it is difficult to derive methane con-tent directly from mass 16, especially in a situation with a small amount of methane in the presence of large amounts 10 of H20 and or C02. However, methane also has a peak at 15 (CH3), which is free from O interference. Although higher alkanes also have a contribution on 15, their contribution to that peak is minor, so 15 is considered to be a clean, i.e., relatively free from interferences, methane peak.
FIGURE 6A also illustratas the occurrence of recurring peaks at about 14 MCR unit intervals. Such recurring peaks are not observable in the linear display of FIGURE 6B, but are advantageous in investigating the subsurface. See EXAMPLE I below.
FIGURE 6, as indicated, is a logarithmic display of MCR abundance in a collective volatiles sample result-ing from summing a plurality (256) of scans of MCR 2-300 for each sample. Both the logarithmic record and the mul-tiple scanning of each sample facilitate identifying the 25 abundance of the trace elements and compounds useful in accordance with the invention for inclusion mapping the earth's subsurface.

,, ., . - . , : . :

J ~

Tllis can be illustrated by reference to FIGURE 6B which shows the data of FIGURE 6A displayed using a linear scale. FIGURE 6B shows that MCR at 16 5 (representing oxygen), 17 (representing ammonia NH3), 18 (representing H2O), 14,28 (representing nitrogen N2), 22,44 (representing CO2), are the most abundant inorganic volatiles in sedimentary fluid inclusions. A methane peak at MCR 15 and other minor hydrocarbon peaks can be 10 observed. It will be apparent that it is useful according to the invention to use a nonlinear, for example, loga-rithmic scaling of the MCR data to enhance MCR responses of trace organic and inorganic volatiles relative to the more abundant components of fluid inclusions.
According to a further aspect of the invention, composition data resulting from analysis of collective fluid inclusion volatiles are displayed as a function of depth along a borehole in the earth. Since the composi-tion data are representative of heterogeneous fluid inclu-20 sions, MCR can be selected representative of particular compounds of interest and displayed relative to other MCR.
Such displays may be referred to as fluid inclusion compo-sition log displays.
In comparing one or more typ~s of molecules to 25 one or more others, such as A to B, it is preferred to determine the ratio A/(A+B). This permits a semiquantita-tive evaluation from well to well. A is said to be nor-.:. , -& .2 malized with respect to B. Either A or B can represent one or more MCR.
Different displays are useful for different pur-5 poses as described in more detail below. Generally, binary displays in which one MCR or group of MCR is com-pared to another MCR or group of MCR are used for fluid inclusions log displays. Such binary displays are useful as displaying relative abundance of one or more compounds 10 to one or more others. Referring to FIGURE 1, by measur-ing and integrating a pressure change during volatiles release, for example, using pressure gauge P, a measure of absolute abundance of the various MCR can also be obtained using the ideal gas law.
Table 5 illustrates some useful binary displays;
however, many other selections for display of relative or absolute abundances of elements and compounds in fluid inclusions can be used in accordance with the invention.
Exemplary mapping uses are shown in Table 5; however, all 20 measures can be used as chemical compartmentalization markers in appropriate cases.

, .

.

B~n~ry Mass/Mass Plots Table 5 Mass/Mass Ratio Compound/Com~ound Mapping Tool Example 5 57/57+15 Paraffin/Paraffin + Methane Oil vs. Gas 57/55+57 Paraffin/Paraffin + Naphthenes Oil vs. Water Inclusion 91/97+91 Toluene/Alkylated Naphthenes Composition of Hydrocarbon in Inclusion 34/15+34 H2S/Methane Productive Faults 34/44+34 H2S/CO2 Productive Faults 15/18+15 Methane/Water Hydrocarbon vs Water In.
57/44+57 Paraffin/CO2 Migration Zones, Seals 10 4/4+2 Helium/Hydrogen + Helium Stratigraphic Marker 28/44+28 Nitrogen/CO2 Paleo Air Zones 15/59+15 Methane/Methane + CO2 Migration Zones, Seals 40/40+41 Argon 40/Hydrocarbon fragment Paleo Air Zones Referring now to FIGURE 8, FIGURE 8 is referred to here to illustrate a binary log display by depth.
FIGURE 8 illustrates variation in mass 15 (meth-ane) to the sum of masses 15 and 44 (methane plus CO2) as a function of location along a borehole. Reference to Table 5 above will indicate that such ratio is indicative of variation in abundance of methane, specifically abun-dance of methane relative to CO2, the most prevalent inor-ganic gas in fluid inclusions.
Another useful form of display is the ternary diagram in which three MCR or groups of MCR for a plural-ity of fluid inclusion samples are displayed relative to25 one another. Useful ternary displays are set forth in Table 6 below; however, many others can be selected in accordance with the invention.

'' -' '',' '. . ' ~': :

Ternary Mass/Mass/Mass Plots Table 6 Mass/Mass/Mass Compound/Compound/Compound 5 91/97/15 Toluene/alkylated Napthene/Methane 34/44/15 H2S/C02/Methane Referring now to FIGURE 7, FIGURE 7 illustrates a ternary mass/mass/mass display of collective fluid inclusion samples along a borehole. Ternary diagrams are useful particularly for recogni~ing chemical compartment signatures or fingerprints since they are readily recog-nized visually. Side 180 represents the ratio of MCR rep-resentative of paraffins to MCR representative of toluene (paraffins/(paraffins plus toluene)); side 182 represents the ratio of MCR representative of methane to MCR repre-sentative of methane plus toluene; and side 184 represents the ratio of MCR representative of methane to MCR repre-sentative of methane plus paraffins.
Each of symbols 186, 188 represent a sample at a depth along a borehole locating the methane, paraffin, toluene components relative abundance in the ternary plot.
Symbols 186 are clustered in a group illustrated by dashed line l90 having a characteristic definable range in the ternary plot whereas symbols 188 are clustered in a group having a characteristic definable range in the ter-nary plot illustrated by dashed line 192.
Group 188 is different in its ranges on the ter-nary plot from group 192. Group 188 is associated with . .
., " . ' , ' ~: ~ :. : '' . ~

~ tJ

deeper formation adjacent borehole levels being investi-gated and Group 192 is associated with shallower levels.
Thus, Groups 188 and 192 are representative of regions of 5 different characteristic inclusion chemistry in the sub-surface and are indicative of different geological histo-ries for the two regions.
Once such groups are identified based on a plu-rality of volatiles samples from a plurality of locations 10 in one or more wells in a region, the groups can be mapped by extent in the earth, for example, as a function of depth or areal extent or both. Moreover, the correspond-ing groups can be identified in other wells in the region and used as indicators of chemical compartments from well 15 to well in an area. This is referred herein as mapping extent of zones in the subsurface each zone having charac-teristic inclusion composition and each zone based on a plurality of volatiles samples from a plurality of locations.
Zones having characteristic fluid inclusion com-positions can be identified using various displays in var-iation of inclusion composition as a function of location in the earth. Such zones can be identified using either binary or ternary or other plots showing variation in 25 inclusion composition among a plurality of fluid inclusion samples from a plurality of locations in the earth.
In a binary plot such zones can be characterized by observing intervals of depths in the subsurface charac-.

.
~-, ~ . , .

terized by relative abundance or lack of ahundance of one or more elements or compounds of interest. The sequence of such zones as a function of depth is also significant 5 and useful in correlating regions from well to well across a field or reservoir. For example, if a characteristic pattern of alternating regions of abundance or lack of abundance of a compound occur across a field, it is indic-ative of shared sequence of geological history across the 10 field. Alternatively, if part of the record pattern repeats from well to well and another part does not, it is indicative of a shared history before or after some geo-logical event, such as faulting, which can often be iden-tified and used in exploring for oil and gas. Finally, if 15 no part of the record pattern is common to two or more wells, it is indicative of different formation histories.
Inclusion mapping of the subsurface has been found to show that different parts of a single geological formation often have regions of significantly different 20 inclusion compositions which are useful in exploring for oil and gas. See EXAMPLE VI below. Moreover, inclusion composition mapping can show common patterns across dif-ferent formations, for example, of hydrocarbon migration.
Hence, fluid inclusion mapping of the subsurface provides 25 highly significant information to the oil and gas explora-tionist which is not provided by conventional strati-graphic information - information indicatinq which regions ~ -- - ~ ~ . : -:; : . .~

in a formation or acxoss formations have shared events in geological history.
After identifying characteristic fluid inclusion 5 regions in the subsurface, such regions can be used as stratigraphic time markers of different fluid environ-ments. Such time markers can cut across geology strata of the same or different ages.
These aspects of the invention are illustrated 10 in EXAMPLES I-IV below representing analysis, using the invention, of a single well.
To summarize EXAMPLES I-IV, fluid inclusion ana-lyses of cuttings from one well indicate zones of hydro-carbon migration, suggest the presence of a seal, restrict 15 timing of hydrocarbon migration, provide two stratigraphic time marker horizons useful on a local scale, and illus-trate two widely occurring stratigraphic fluid inclusion horizons which may be useful on a worldwide basis.
EXAMPLES I-IV are the result of the analysis in 20 accordance with the invention of 90 well cuttings samples in 3-1/2 hours.
EXAMPLE I - HYDROCARBON MIGRATION ZONES AND SEALS
The fluid-roc}c interaction of most interest to oil and gas explorationists is hydrocarbon migration.
25 FIG~RE 8 is an example of a typical fluid inclusion log, showing depth versus some aspect of fluid inclusion compo-sition, in this case abundance of methane, specifically of methane to CO2, i.e., methane/(methane + CO2). This ratio .. ' ,: ' ' "
~ ' :

has been multiplied by 100, and is therefore plotted as a percentage. The highest possible value for X on a plot of this nature is 100, and the lowest is 0. This plot con-5 tains much information about hydrocarbon migration throughthe rocks penetrated by the well. Methane and carbon dioxide are the two most abundant gases in the subsurface.
Both are based on carbon -- methane being the most reduced compound and C02 being the most oxidized compound. Com-10 pared to water, C02 is the next most abundant inclusioncompound in the subsurface, but is easier to analyze.
Hence, ratioing CH4 to CO2 provides a relative estimate of methane abundance in the subsurface which can also be used for comparing different wells in an area.
Very high values of methane relative to CO2 are found between about 14,500 and about 17,000 ft as indi-cated by reference numeral 150. The presence of methane and other hydrocarbons in inclusions in this section of rock indicates that a fluid hydrocarbon phase migrated 20 into these rocks, some of which was trapped as fluid inclusions. As indicated by reference numeral 152, between 13,000 and about 14,500 ft is a zone with very little methane. The lack of hydrocarbon inclusions in the section of roc~ 152 immediately overlying the zone 150 25 suggests that zone 152 is a seal. This interpretation, based on the inclusion data, is supported by the fact that the only gas show found in this well occurred in the zone 150 having methane-rich inclusions suggesting trap-.- ~ .

: ~:
. :
:

ping of hydrocarbons by zone 152. Gas shows, of course, are representative of pore system fluids and not of inclu-sion fluids. An intermediate value of methane/(methane +
5 CO2) is observed between about 3000 and 13,000 ft indi-cated by reference numeral 154. The methane content in zone 156 from the surface to about 3000 ft is very low.
The intermediate methane content of the inclu-sions in zone 154 between 3000 and 13,000 ft suggests 10 hydrocarbon miyration into these depths, as well as into zone 150 between 15,000 and 17,000 ft. The lack of sig-nificant methane in zone 156 between the surface and 3000 ft suggests hydrocarbon did not migrate through this zone. The break at 3000 ft between zones 154 and 156 cor-15 responds to the Cambrian-Precambrian unconformity. Sand-stones are found on both sides of this unconformity, and there is no petrophysical evidence that this surface is a seal. Taken together, these data suggest that hydrocarbon migration, at least through zone 154 between about 3000 20 and about 13,000 ft, occurred prior to the deposition of the Cambrian sands of zone 156.
Referring now to FIGURE 9, FIGURE 9 shows the mass spectrum of collective inclusion volatiles ~rom 16,000 ft in the well illustrated in FIGURE 8. Hydrocar-25 bons at least well out into the gasoline range areobserved. Since inclusion gases are subject to the same thermal stresses experienced in the open-pore system and hydrocarbons are observed out into the gasoline range, .. . .

.

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indicating no thermal cracking, the data in FIGURE 9 sug-gest the rocks in zone 150 did not reach catagenetic or breakdown temperatures. It is noted that this interpreta-5 tion would be difficult or impossible using a display suchas that of FIGURE 6B.
EXAMPLE II - SUBAERIAL EXPOSURE ZONES
Paleo-vadose zones, and therefore paleo-exposure zones, can be rapidly identified using automated fluid 10 inclusion volatile analyses in accordance with the invention. Vadose zone sediments include all sediments above the water table during mineral formation. The pores in sediments in the vadose zone are occupied by a mixture of atmospheric air and water.
Paleo vadose zones are conventionally recognized through a combination of petrology and stable isotope chemical stratigraphy. Carbonates that form in the vadose zones have characteristic cements called "meniscus" and "pandant". Petrographic identification of these cements 2~ is positive evidence of paleo-vadose environments.
Also, vadose zones have characteristically light Carbon-i~otope signatures. The isotopically light Carbon found in the vadose zone is derived from rotting vege-tation. These data are u3ed to define paleo-vadose zones.
25 Although these technique~ can be definitive they are very time consuming, and involve considerable sample prepara-tion.

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Cements that form around and between minerals in the vadose zone trap variable amounts of air and water in fluid inclusions. Petrographic identification of inclu-5 sions having variable amounts of air and water can there-fore also be used to identify paleo-vadose zones.
However, this technique is also extremely time consuming, and requires considerable sample preparation.
A rapid method of identifying paleo-vadose zones 10 is by automated analyses of volatiles in fluid inclusions according to the invention.
Inclusions that form in vadose environments trap small amounts o~ air. A characteristic gas in air that does not occur in the subsurface is molecular oxygen, 15 Argon, Xenon and the like, i.e., ~2' Ar, Xe. The autosampler/mass spectrometer system in accordance with the invention rapidly identifies those samples that con-tain these molecules in inclusions. Vadose zones that have been identified in this fashion, i.e., by the pres-20 ence of molecular oxygen or Argon or Xenon in fluid inclu-sions, have been confirmed by petrographic and isotopic investigations.
Documenting paleo-vadose zones is important in exploration for oil and gas inasmuch as it documents paleo 25 exposure zones. A regional study of paleo exposures can permit the delimitation of paleo-shore lines, as well as paleo topography, inasmuch as water tables follow topogra-phy. A knowledge of paleo topography can be used in : ., : . .
. ; ~ , .

exploration for reservoired hydrocarbons trapped along ~mconformities. Further, paleo exposure zones are often either zones of porosity enhancement or porosity 5 destruction. Zones of porosity enhancement are potential reservoirs, zones of porosity destruction are potential seals. Hence, a method for rapidly and easily identifying paleo exposure zones in the subsurface provides great advantage to the oil and gas explorationist.
Referring now to FIGURE 10, FIGURE 10 shows the variation of argon content in the inclusions mass ratio 40/41+40 as ~unction of depth. Argon has mass 40 and is somewhat masked by presence of adjacent hydrocarbon fragments. Hence, one of these fragments, such as MCR
15 fragment ratio 41, is selected for comparison to remove to some extent effects of hydrocarbon from argon response at 40. Note the presence of two positive anomalies, zone 158 between 13,000 and 15,000 ft, and zone 160 between 8,500 and 9,500 ft. These zones are also found to show high 20 abundances of nitrogen and molecular oxygen (logs not shown). Molecular oxygen is a gas only found at the earth's surface, and as such is a direct indicator of sub-aerial exposure. Nitrogen is the most abundant atmo-spheric gas, and argon is a diagnostic trace atmospherlc 25 gas. The dissolved argon, nitrogen, and oxygen contents of surficial waters are very low, especially compared to atmospheric abundances. These two argon-enriched inclu-sion zones can therefore be considered indicators of .. ~ .
., ,. --- .
- ,, , . , -, paleosubaerial exposure surfaces. The lower exposure zone 158 corresponds to the hydrocarbon seal (zone 152) indicated in FIGURE 8. Therefore, this surface is indi-5 cated to be a sealing exposure zone. The argon-enriched inclusion zone 160 around 9000 ft has methane contents that are not noticeably different from the stratigraphi-cally-higher and lower Precambrian sands (see FIGURE 8).
This zone is indicated to be a nonsealing exposure zone.
Independent evidence is obtained that suggests zones 158 and 160 are subaerial exposure surfaces. The lower zone 158 is composed of a red, fine-grained silt-stone. The red color of this siltstone suggests an oxi-dized nature, consistent with it being an exposure zone.
15 The fine-grained nature of this siltstone is also consist-ent with the sealing hypothesis. A core from the upper zone 160 was studied and described as an Eolian sequence, which is by definition a subaerial exposure zone. If these exposure zones are laterally extensive, then their 20 inclusion signature will provide a stratigraphic time marker in the basin.
EXAMPLE III - CAMBRIAN/PRECAMBRIAN UNCONFORMITY STRATI-GRAPHIC MARKER
Referring now to FIGURE 11, FIGURE 11 shows var-25 iation in nitrogen relative to CO2 in the well. A break or transition between two zones is indicated by reference numeral 162 at about 3000 ft, at the Cambrian-Precambrian unconformity. The Precambrian rocks in the zone below ,, ~
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break lfi2 are enr:iched in nitrogen relative to the Camb-rian rocks above break 164. This behavior is found repeatedly at Paleozoic-Precambrian unconformities.
5 F:[GURE 12 shows the same pattern in another well at refer-ence numeral 164.
Analyses of fluid inclusions in well cuttings appears to indicate the Paleozoic-Precambrian unconformity on the basis of nitrogen content - Precambrian sediments 10 have nitrogen-enriched inclusions, and Paleozoic inclu-sions are nitrogen depleted, therefore providing a Pre-cambrian stratigraphic marker~ Without limiting the invention, thls pattern hypothesized to be due to the explosion of life at the beginning of the Paleozoic. The 15 accumulation of extremely large amounts of biomass resulted in the removal of nitrogen from the atmosphere, and subsequently a decrease of dissolved nitrogen in waters trapped in fluid inclusions. This may be a world-wide stratigraphic horizon.
EXAMPLE IV - HELIUM PRECAMBRIAN STRATIGRAPHIC MARKER
FIGURE 13 shows variation of helium content of inclusions in the well. A measure of helium in the sub-surface is obtained by using the rakio of 4/4+2. Both helium and deuterium contribute to the peak at 4; but only 25 hydrogen contributes to the peak at 2. The abundance of deuterium varies with the abundance of hydrogen. Hence, the ratio 4/4+2 can be used to remove to some extent the effects of deuterium on the peak at 4. Note that the .

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helium contellts increase very rapidly in zone 166 below 13,000 ft. Similar variations are found in wells that tested the upper Precambrian in other wells worldwide.
5 Helium contents of this magnitude have not been observed in analyses of younger rocks. In younger rocks that have helium in some inclusions, such stratigraphically-thick helium-enriched sections have not been observed. Detailed petrographic analyses of sandstones from the well shows no 10 noticeable petrophysical change near the abrupt increase in helium content. Red sandstones having hematite cement occur above and below this helium transition. This helium marker, therefore, provides a Precambrian stratigraphic time marker.
Without limiting the invention, this change in helium content of the fluid inclusions is hypothesized to be a result of changing oxidation states of the earth's atmosphere. Helium-rich inclusions are hypothesized to occur in sediments deposited when the earth's atmosphere 20 was sufficiently reducing so that uranium valence state was such as to render it relatively insoluble in water.
Under these conditions, uranium would be deposited as detritus. Uranium varied with the original sediment could produce helium throughout time by radioactive decay. This 25 helium could be trapped as fluid inclusions once liber-ated, or if small amounts of uranium were trapped as solid inclusions, the helium would be trapped in the same inclu-sion. Under more oxidizing atmospheric conditions, ura-:

: '~' ' '~ . .

ni~m would be soluble in water, and would not be deposited as detritus. Therefore, helium-rich inclusions would not be expected.
EXAMPLE V - TRAPPING FAULT AND MIGRATION IDENTIFICATION
This EXAMPLE illustrates the use of fluid inclu-sion stratigraphy for identifying trapping and nontrapping faults.
Referring now to FIGURE 14A, FIGURE 14A repres-10 ents a well 350 testing a simple fault trap. As illus-trated the well has cross faults A and B (illustrated by arrows 352 showing relative movement of various strata 354) missing oil trapped in reservoirs R upthrown to ~ault A. It is not known whether fault A is a trapping 15 fault.
Referring now to FIGURE 15B, FIGURE 15B illus-trates a log display 356 of paraffin abundance in fluid inclusions as a function of depth adjacent wellbore 350.
The log display is smoothed and generalized for simplic-20 ity.
Between faults A and B, curve 356 shows there isa zone of relatively high paraffin content. The return to lower values of paraffin above fault A indicates that fault A is a trapping fault. The return to lower values 25 of paraffin below fault B indicates fault B may be the migration pathway along which oil migrated into traps R.

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EXAMPLE VI - SUBTLE STRATIGRAPHIC TRAPS
This ~XAMPLE illustrates that fluid inclusion stratigraphy can be used for locating subtle stratigraphic 5 txaps within a formation. FIGURE 15A is a structure con-tour map of the topographic top of a producing formation.
Production wells #3, #4, ~5 occur in the region. Ternary diagrams showing variations in fluid inclusion compos-itions for various wells in and around the field of 10 FIG~RE 15A are shown in FIG~E 15C. These ternary dia-grams show the relative variations of masses 15 (methane), 44 (CO2), and 41 (an oil fragment). The intensity of mass 41 was multiplied by a factor of 10 prior to plot-ting. Note that all the producing wells ~3, #4, #5 in the 15 field show very similar fluid inclusion composition pat- ~-terns. A down-dip dryhole #6 shows fluid inclusion com-positions also very similar to those found in the field.
Two wells #1, #2 north of a barrier to hydrocarbon migration line 238 have inclusion compositions distinctly 20 different ~rom those of producing wells #3, #4, #5 in the field, but similar to each other. One of these two wells produce water updip to oil.
The field could have been located using fluid inclusion analyses of the three dryholes ~ust mentioned.
25 The similarity of the inclusion data for wells #1 and #2 provides no encouragement for continued exploration in between them. However, the marked difference in fluid inclusion composition between these two wells and the well ' " - : ~ ' ' ~ ' ~ :-:

#6 indicates some sork of subsurface chemical compartmen-talization, suggesting the possibility of a trap between these wells. Exploration between the wells #6 and wells 5 #1 and #2 would have resulted in the discovery of the field.
Referring now to Figure 15B, FIGURE 15B illus-trates percent C02 to C02 plus methane in inclusions for wells #l through #6. Wells ~1 and #2 are similar to one 10 another but differ from wells #3, #4, and #5 which are self~similar, and from well #6. If during prediscovery, wells #1, #2, and #6 had been drilled and found nonproduc-tive (as indicated by stippling in FIGURE 15B), fluid inclusion analysis in accordance with the invention would 15 have suggested that a potential trap existed between the wells due to the contrast in C02 incl-~sion contents. Sub-sequent drilling between wells #2 and #6 at virtually any location would have resulted in discovery of the field.
FIGURE 15D illustrates ternary diagrams of ~0 FIGURE 15C displayed relative to formation map 15a.
EXAMPLE VII - FLUID INCLUSION STRATIGRAPHY
Thirteen complete wells are analyzed in an area.
A repetitive fluid inclusion stratigraphy i.e., different zones each having characteristic fluid inclu~ion compos-25 itions, is seen in many of these wells. For example, byconsidering the variation of paraffins relative to meth-ane, a zone of low paraffin abundances are found shallow and deep, and a zone of abundant paraffins is found at :: - , . , ., .

some intermediate depths. The paraffin-rich zone is several thousand feet thick. Porous sands are found gen-erally to occur within, above, and below these paraffin-5 enriched zones. Thus, the paraffin-enriched zones are not coincident with normal stratigraphy from well to well.
The tops and bottoms of these paraffin-enriched inclusion zones are found usually to be fault-bounded. In wells having oil shows, the "oily" inclusion zones are found to 10 extend thousands of feet below the deepest reported show.
The consistency of these blocky inclusion pat-terns from well to well argues for a general genetic proc-ess. The bottom of these 20nes is determined to mark the basal hydrocarbon migration pathway in that well, and the 15 top to mark a barrier to hydrocarbon migration. It is assumed that vertical migration may occur within these zones.
Preliminary data show that the basal migration pathway becomes shallower both to the east and west of the 20 field. These data suggest the specific fault systems may be the main conduits in the field. The basal migration pathway may be predictive as to the maximum productive depth in an area.
EXAMPLE VI I I - DETERMINING DIRECTION OF OIL ACCUMULATIONS
BY MEASURING DIFFUSED AROMATICS IN FLUID INCLUSIONS
All of the various aspects of the invention relate at least in part to stratigraphic mapping of the subsurface using composition data of collective fluid -.
.

~2~d inclusion volatiles. The heterogeneous mixtures of gases, as has been shown, are a powerful tool for mapping and interpreting the subsurface - a tool which permits mapping 5 chemical compartmentalization independently of knowledge of geological structure in the earth, but which greatly assists in interpreting geological structure.
Aromatics are known to diffuse outwardly from oil accumulations forming an abundance gradient. Fluid 10 inclusions are formed on an ongoing basis. This suggests tha-t measurement of fluid inclusion aromatics can ~e used to identify the direction of oil accumulation.
For a known oil accumulation analysis using the invention determined toluene versus toluene plus CO2 15 ratios (representative of abundance of toluene). The resulting data show an increase in the toluene/(toluene plus CO2) ratio in the direction of the oil accumulation.
This EXAMPLE illustrates usefulness of the invention for identifying direction of oil accumulations.
EXAMPLE IX - RESERVOIR AND FAULT DETECTION
FROM FLUID INCLUSION COMPOSITIONS
This EXAMPLE illustrates the use of fluid inclu-sion composition zones for mapping a particular field.
Fluid inclusion composition data from core sam-25 ples and drill cuttings from five wells in an area are used to map a field in accordance with the invention.
Detailed sampling of core (one sample per foot) from productive and nonproductive thrust sheets allows ':

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p:Lotting of fluid inclusion compositional data where vari-ations in lithology and porosity are well-known. Refer-r:ing to FIGURE 16A, FIGURE 16A illustrates a ternary plot 5 in accordance with the invention of C02/CH4/H2S showing characteristic composition patterns for porous sandstone, shale and nonporous sandstone.
FIGURE 16B illustrates a ternary plot of C02/CH4/H2S showing characteristic inclusion compositions 10 for productive and nonproductive thrusts. These data indicate adequate fluid inclusion chemical compartmentali-zation for using fluid inclusion analysis in this field for distinguishing these geological features.
Referring now to FIGURE 16C, FIGURE 16C illus-15 trates a log display in accordance with the invention ofH2S (normalized relative to C02) as a function of depth.
The high H2S zones 270, 272, 274 are found to occur on thrust sheets with good shows or producible gas reser-voirs. The H2S plots do not distinguish between economic 20 and uneconomic gas accumulations in this field.
Referring now to 16D, FIGURE 16D illustrates variation in C02/C02 plus CH4 for a well. The C02 anoma-lies 276, 278, 280, 282, 284 are negative and in sandstone intervals containing porous zones. By identifying updip 25 porous zones, new zones are identified for production testing. This illustrates use of the invention for locat-ing porosity zones.

-Referring now to FIGURE 16E, FIGURE 16E illus-trates variations in helium/(helium plus hydrogen). Posi-tive helium anomalies 286, 288, 290, 292, and 294 are 5 found by comparison with seismic data, to occur in thrust fault zones. This illustrates use of the invention to aid in identifying thrust zones.
The positive helium anomalies occurring at thrust fault zones occur whether or not the thrust fault 10 is productive.
This E~AMP~E indicates that for this field, hydrogen sulfide anomalies occur in productive thrust sheets, carbon dioxide anomalies occur in porous sand-stone, and helium anomalies occur in thrust salts.
These characteristic fluid inclusion signatures can be used to map these zones in other wells in the field and may be generalizable to other fields.
EXAMPLE X - MAPPING STRUCTURAL FEATURES EROM
ELUID INCLUSION COMPOSITION DATA
This E~AMPLE illustrates use of fluid inclusion composition zones for identifying structural features in a field.
Seven wells in the study area were selected for analysis and ternary plots of various elements are found 25 to distinguish from updip platform, downdip lagoonal lime-stone, and porous rock (gas or water filled).
Fluid inclusions in updip platform rocks have relatively high saturations of methane.

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Fluid inclusions in bitumen-filled foreslope facies can easily be distinguished as being enriched with toluene and hydrogen sulfide (H2S).
Fluid inclusions in the lagoonal limestones are enriched in carbon dioxide (C02) and depleted in methane.
Fluid inclusion in late stage calcspars are depleted in methane, and enriched in H2S or HCl plus (more saline).
Using these characteristic compositions, the field can be mapped as a function of the identified zones.
In the course of making the invention in its various aspects, many problems were solved.
A system was developed for individually crushing 15 and analyzing inclusion contents of a plurality of sam-ples. Crushing of samples was made to occur in a contin-uously pumped vacuum to speed processing and to ensure that freshly released volatiles absorbed as little as pos-sible to surfaces exposed by crushing. There was devel-20 oped means for keeping a plurality of samples separate,while crushing each of them separately under a vacuum.
For efficiency, a system was developed for using a smaller number of crusher means for crushing samples than there were samples and also means for moving samples into posi-25 tion for crushing. The system was made to be sturdyenough for repeated use. Released volatiles were quickly delivered to analysis means for producing an adequate record of most all of the elements and compounds present . ,.,: : ' ~ . :

: :

for chemical inclusion zone mapping of the subsurface.
Analytical instrumentation itself was developed to detect the low amounts of trace elements and compounds present in 5 fluid inclusions which, as described above, confer many significant benefits on oil and gas explorationists. The large amounts of resulting composition data were stored in retrievable form. The resulting data representative of heterogeneous mixtures of elements and compounds released 10 from myriad inclusions in each sample were processed and interpreted and various displays by depth and areal location were developed to assist in interpretation and use of the data.
Using the invention in its various aspects has 15 permitted analysis and interpretation of fluid inclusion compositions in three dimensions in the earth's crust, that is, in both a vertical and lateral sense. Fluid inclusion stratigraphy of sedimentary formations has been subject to such difficulties in obtaining adequate data 20 for the numerous microscopic (typically <10 microns) fluid inclusions present that it has not previously been seri-ously attempted or contemplated by others.
Use of chemical fluid inclus.ion mapping of the subsurface has permitted mapping o~ oil/gas migration 25 pathways, placing timing constraints on oil/gas migration, demonstrating multiple episodes of oil/gas migration, locating seals, locating faults, demonstrating fluid migration along faults, locating unconformities, locating . . .. . . . ..

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paleo-exposure surfaces (paleovadose zones), estimating thermal exposure ~hydrocarbon maturation and catagenesis), and providing time horizons ~stratigraphic time markers) 5 in various sediments. Many other advantages can also be obtained.
Fluid inclusion stratigraphy in accordance with the invention is a rapid technique based on the analyses of hundreds or thousands of samples per day for fluid lO inclusion volatile composition. It is this speed and ease of data acquisition that makes these types of studies pos-sible.
The invention has been described in terms of preferred embodiments and specific applications but is not 15 limited thereto, but by the claims appended hereto and is entitled to the full range of equivalence permitted by law.

, :. . . -: , - .
:. .:. - :

Claims (21)

1. Apparatus, including controller means, for releasing, delivering, and analyzing composition of a plurality of collective fluid inclusion volatiles samples comprising:
releasing means for sequentially and individually releasing a collective fluid inclusion volatiles sample from each of a plurality of sedimentary rock samples;
analytical means for determining composition of each collective fluid inclusion volatiles sample;
delivery means for delivering each collective fluid inclusion volatiles sample from releasing means to analytical means; and controller means for causing each collective fluid inclusion volatiles sample to be sequentially and individually released by the releasing means and for causing each collective fluid inclusion volatiles sample to be sequentially and individually analyzed by the analytical means.

2. The apparatus of Claim 1 wherein the releasing means comprises:
an evacuable chamber;

releasing means within the evacuable chamber for releasing a collective fluid inclusion volatiles sample from myriads of fluid inclusion in each rock sample;
and positioning means within the evacuable chamber for positioning each rock sample relative to the releasing means;
and wherein controller means comprises:
means for generating a signal causing positioning means to position a selected rock sample relative to releasing means for releasing a collective fluid inclusion volatiles sample from the selected rock sample;
means for generating a signal for causing releasing means to release the collective fluid inclusion volatiles samples from the resulting positioned rock sample;
means for generating a signal for causing analytical means to analyze composition of gases in the evacuable chamber including the collective fluid inclusion volatiles samples; and means for effecting sequential operation of the previously defined means for each of the plurality of rock samples.

3. The apparatus of Claim 2 wherein the means for effecting sequential operation comprises:

means for determining whether a collective fluid inclusion volatiles sample has been released from all of the plurality of rock samples;
means responsive to means for determining for generating a signal for positioning a further rock sample relative to releasing means effective for releasing means releasing a collective fluid inclusion volatiles sample from the further rock sample;
means for generating a signal for causing releasing means to release the collective fluid inclusion volatiles sample from the further rock sample; and means for terminating sequential operation responsive to a condition that a collective fluid inclusion volatiles sample has been released from all of the plurality of rock samples.

4. The apparatus of Claim 1 wherein the analytical means comprises:
mass spectrometric means for determining mass to charge ratio (MCR) responses of a collective fluid inclusions volatiles sample on an MCR by MCR
basis;
means for causing mass spectrometric means to scan a range of MCR responses a multiplicity of times during time of a collective fluid inclusion volatiles sample being provided to mass spectrometric means;

means for summing MCR responses for all of multiplicity of scans for each rock sample on an MCR
by MCR basis; and means for storing summed MCR responses as a record of composition of the collective fluid inclusion volatiles sample for the rock sample.

5. The apparatus of Claim 4 wherein the analytical means further comprises:
conduit means for receiving a collective fluid inclusion volatiles sample from the releasing means, said conduit means being open to the releasing means prior to and during release of the collective fluid inclusion volatiles sample;
and wherein the controller means further comprises:
means for generating a signal for causing mass spectrometric means to scan a range of MCR
responses a multiplicity of times during a period of time prior to release of collective fluid inclusion volatiles samples;
means for generating a signal for causing the mass spectrometric system to scan a range of MCR
responses a plurality of times during release of collective fluid inclusion volatiles sample; and means for causing means for summing to sum responses produced by multiplicity of scans prior to release of volatiles sample to produce a background record and for causing means for summing to scan responses produced by multiplicity of scans during release of volatiles sample to produce a sample record.

6. The apparatus of Claim 4 having mass spectrometric means configured as follows:
first mass spectrometric means configured for sampling most abundant MCR represented in fluid inclusion volatiles samples including at least carbon dioxide, water, and nitrogen;
at least second mass spectrometric means configured for sampling MCR less abundant than those sampled by first mass spectrometric means.

7. The apparatus of Claim 4 wherein:
means for causing mass spectrometric means to scan is effective for a multiplicity of scans in the range from about 100 to 1000 during time characteristic of release of collective fluid inclusion volatiles samples.

8. The apparatus of Claim 4 wherein:
mass spectrometric means comprises a plurality of signal conditioners having different input ranges and further comprising:
means for selecting a signal conditioner for each MCR response.

9. The apparatus of Claim 4 comprising:

bank of MS adapted for measuring substantially all MCR in range from about 2 to about 60 MCR.

10. The apparatus of Claim 4 comprising:
bank of mass spectrometers adapted for measuring substantially all MCR in range from about 2 to about 120 MCR.

11. The apparatus of Claim 4 comprising:
bank of mass spectrometers adapted for measuring substantially all MCR in range from about 2 to about 300 MCR.

12. The apparatus of Claim 4 wherein means for summing comprises:
array of signal conditioners for each mass spectrometer, each array providing an output in one of a series of amplitude ranges for each determinate MCR measured by such mass spectrometer;
analog to digital converter means connected to array of signal conditioners for converting output from analog to digital form;
computer for receiving digitized MCR and for summing each MCR in a respective MCR memory on MCR by MCR basis for the multiplicity of scans; and means for producing a record as a function of MCR of summed MCR for the multiplicity of scans.

13. A method of controlling apparatus comprising an evacuable chamber, releasing means within the evacuable chamber for releasing a collective fluid inclusion volatiles sample from positioned rock samples, positioning means within the evacuable chamber for positioning each of a plurality of separate rock samples relative to the releasing means and an analyzer connected to the evacuable chamber for receiving released collective fluid inclusion volatiles therefrom for determining the composition thereof, the method comprising:
generating a signal for causing a rock sample to be positioned relative to releasing means effective for releasing means releasing a collective fluid inclusion volatiles sample from the positioned rock sample;
generating a signal for causing releasing means to release the collective fluid inclusion volatiles sample from the positioned rock sample;
generating a signal for causing analyzer to determine composition for collective fluid inclusion volatiles released by releasing means; and repeating the preceding three steps for each of the plurality of rock samples.

14. The method of Claim 13 wherein the repeating step comprises:
determining whether a collective fluid inclusion volatiles sample has been released from all of the plurality of rock samples;
responsive to a condition that not a collective fluid inclusion volatiles sample has not been released from all of the plurality of rock samples, generating a signal for positioning a further rock sample relative to releasing means;
generating a signal for causing releasing means to release a collective fluid inclusion volatiles sample from the further rock sample; and responsive to a condition that a collective fluid inclusion volatiles sample has been released from all of the plurality of rock samples, terminating the repeating step.

15. The method of Claim 13 wherein the step of generating signals for causing analytical means to analyze composition of collective fluid inclusion volatiles released by releasing means comprises:
generating signals for causing analysis of composition of gas in the evacuable chamber prior to and also subsequent to generating a signal for causing releasing means to release a collective fluid inclusions volatiles sample from each rock sample.

16. The method of Claim 13 further comprising:
storing analysis data generated prior to and subsequent to generating a signal for causing releasing means to release a collective fluid inclusion volatiles sample from each rock sample.

17. The method of Claim 13 further comprising:
effecting a preliminary data reduction for collective fluid inclusion volatiles released from each separate rock sample by removing effect of composition data of gases present in evacuable chamber prior to releasing volatiles from each rock sample from composition data of gases present in evacuable chamber subsequent to releasing volatiles from each rock sample.

18. A method of analyzing composition of a collective fluid inclusion volatiles sample, the sample being a heterogeneous mixture of volatiles released from myriad fluid inclusion in a rock sample, the method comprising:
providing at a predetermined time a collective fluid inclusion volatiles sample to mass spectrometric means for mass spectrometrically analyzing composition thereof;
scanning, using mass spectrometric means, a range of mass to charge ratio (MCR) values a multiplicity of times during time sample is being provided to mass spectrometric means;
summing results of mass spectrometric scans on an MCR by MCR basis for all of the multiplicity of scans; and storing summed results for all scans on an MCR by MCR basis, wherein summing the multiplicity of scans is effective for integrating MCRs characteristic of the sample during delivery of the volatiles sample to the mass spectrometric means.

19. The method of Claim 18 further comprising:
providing the volatiles sample by releasing a collective fluid inclusion volatiles sample from a rock sample in an enclosure maintained in open flow communication with mass spectrometric means prior to and during releasing the volatiles samples; and conducting the scanning, summing, and storing steps prior to and during releasing of the volatiles sample, producing respectively a first scanned and summed MCR by MCR record and a second scanned and summed MCR by MCR record.

20. The method of Claim 19 comprising:
performing the providing and conducting steps for a plurality of collective volatiles samples;
maintaining enclosure in open flow communication with mass spectrometric means during performing step.

21. The method of Claim 19 comprising:
subtracting, on an MCR by MCR basis, the first scanned record from the second scanned record.