**Total Organic Carbon** content ("TOC") of a source rock ("SR") can be determined in the laboratory from a sample. In such analysis the non-organic Carbon content, such as in carbonates, is removed. Measuring the Carbon dioxide resulting from combustion then results after some calculation in the dry weight percent TOC.

The TOC consists of an inert part (e.g. charcoal particles, inertinite) and a part that is associated with kerogen that can be converted into oil and gas. There are various views on what the minimum amount of TOC is for qualifying as an effective SR. The author assumes that any TOC below 1.5% is doubtful to contribute to expelled oil. At low levels of TOC, oil and gas may be formed within the SR, but may not be sufficient to be expelled, a minimum amount being required for primary migration. However, the small amounts of oil generated in the SR will remain there when the SR is matured further, eventually transformed into gas that finally may be expelled. It could be argued that for gas SRs, there will be often more inert Carbon, so the threshold might have to be higher.

Because of the threshold level of TOC before effective expulsion takes place, it is important to recognize a TOC **"cutoff"** value based on the above reasoning, such as the 1.5% used in the GAEAP50 prospect appraisal program.

Organic material that contains the TOC is lighter than the usual rock mineral components, such as quartz and carbonates. Also the speed of sound is considerably less than in the mineral grain framework. Organic material is also a poor electricity conductor, especially when it contains generated oil. These properties make it possible to detect the presence and amount of organic material in a rock from wireline measurements, under favourable circumstances. The logs that are useful in a wide variety of circumstances are the resistivity log, the density log and the sonic log.

The SRLOG program uses a combination of density/resistivity or sonic/resistivity to estimate the amount of TOC.

**Density log**

The effect of organic material on the bulk density can be calculated by assuming that the bulk density is the result of the density of the various components in the rock: mineral matrix, fluids, kerogen.

For the **density log** the effect calculation is complicated by the fact that TOC is a weight percent while the proportions of components relevant to the log effect (matrix, kerogen and pore fluid in the SR) have to be expressed as volumes.

In the first place the wt% TOC must be related to the wt% kerogen. The ratio of TOC wt% to wt% organic matter is called "r" and will normally vary between 1.0 for an overmature SR to 1.5 for an immature SR.

The density of organic material (o varies from 0.9 to 1.05, depending on type of SR and maturity.

and switching to organic matter:

In the following the formulas will be simplified by using the following symbols:
V_{b} = Bulk rock volume

V_{m} = Matrix volume

V_{o} = Volume of organic material

V_{f} = Volume of fluids (water in porosity)

por = Porosity fraction

ρ_{b} = Bulk density

ρ_{m} = Matrix density

ρ_{o} = Organic matter density

Then, considering volumes:

Simplifying:

V_{m} can be expresses as

Substituting this in (4) and solving for V_{o} gives:

The bulk density is:

or:

Formulas (8) and the substitution (6) for V_{o} can show the effect on density of various contents of TOC. (Note that TOC in these formulas are fractions, not percentages).

Small changes in TOC have a surprising effect of on the bulk density. So, under ideal circumstances, the densilog should be a good tool to evaluate source rocks. Unfortunately, in practice, the densilog is affected by borehole roughness, measuring mud density rather than formation density (over estimation of TOC) in some cases, and presence of pyrite, which masks the effect of light organic material (under estimation of TOC).

Density is partly determined by **compaction**. To estimate TOC the state of compaction must also be known, or eliminated in some way. The easiest way is to use a resistivity/density crossplot to circumvent measuring of the compaction state (Meyer & Nederlof, 1984).

**Sonic log**

The **sonic log** gives the **"slowness"** (transit times) of the sound in terms of microseconds per foot, or microseconds per meter. This is usually indicated by Δt. The effect of organic material on the slowness is studied by assuming that it replaces matrix. One could also consider it as filling part of the pore space, but it is more convenient to group organic material with the also non-conductive mineral matrix.

Wylie's "time-average" formula is:

Δt

Δt

Having part of the solids as organic material, the time-average formula becomes:

or

where Δt_{o} is the slowness of the organic material. This is unknown, but likely to be on the order of 200 microseconds per foot.

The Δt is a function of porosity (compaction) and of depth (c.q. pressure). To estimate TOC, the state of compaction has to be known, as is the case for the use of the densilog. By using crossplots of transit time versus resistivity the state of compaction is eliminated. In practice, a multiple regression equation replaces the crossplot.

The above theoretical effects do not immediately provide a way to estimate TOC in practice. As mentioned above, the state of compaction is required as a basis for the estimate. We should know how far density or transit time deviates from that of a barren rock at the same state of compaction. There are various schemes to do this. Meyer & Nederlof (1984) used sonic and density/resistivity crossplots, but only give formulas for a simple classification into SR or non-SR. The method proposed by Passey et al. (1990) is probably one of the best, but requires making overlays of logs, scaled in a particular way as well as determining the maturity of the section in terms of LOM (Level of Organic Metamorphism).

My SourceLog program will be less accurate than quite a few of the more elaborate methods proposed over the last decade, but is useful for a first screening of logs at least. It is based on data sets from literature where depth, TOC, resistivity, c.q. density was available. A multiple regression has provided two equations: one for the density/resistivity and one for the sonic/resistivity method. In essence, it an extension of the Meyer & Nederlof (1984) method, but then a TOC estimator. After 1984 a host of papers have addressed the petrophysical possibilities, and not least Schlumberger ( such as: Schmoker and Hester, 1983, Fertl, & Chillingar, 1988, Passey et al., 1990 and Gonzalez et al., 2013)

In this method, rather than correcting the measured resistivity to a particular standard temperature, it uses the depth as a third variable that in a gross manner takes care of the temperature effect on resistivity.

The data are from a very wide variety of areas and circumstances. Therefore the derived equations should be widely applicable, however, with the penalty that the accuracy will be low compared to the same method based on a local calibration.