Frequently Asked Questions

WARNING: We DO NOT ACCEPT samples with enriched 14C (often used as a tracer).  Any contamination of any amount of enriched 14C ("hot") material may cause thousands of dollars in clean-up and other costs. If you submit "hot" samples to this lab, you may be liable.

  • Plan for a normal turn around time of about 3 months.  We always try to get samples done sooner if at all possible.
  • Yes, you can pay via credit card (VISA or Mastercard)
  • A purchase order (PO) number is required only if your institution demands it.
  • Samples are not returned unless prior approval and special arrangements are made with the Lab. You are responsible for the shipping and an extra fee for packing up and sending the samples.
How to pack samples for shipping.
  • Include a copy of the submission form inside the box with your samples (and the reference number of the job if possible). Reception at times removes outer labelling and we are left with nothing to ID the samples.
  • DO NOT SHIP GLASS-ON-GLASS!!! Either wrap each vial or bottle individually with bubble wrap or other padding, or make sure there is a layer of cardboard between each (if less than 50 ml) and that the content is packed tightly (no movement within the box or boxes).
  • Make sure that lids will not vibrate loose; wrap lids with tape or Parafilm.
  • DO NOT USE ICE CUBES for samples that need to be kept cool (not even in baggies). They melt, make a mess, and can destroy labels.  A courier may refuse to handle a leaking package, especially if there is a preservative added to the samples. 
  • Insulate the entire shipment in cold weather to prevent freezing and breakage of liquid samples.
  • If you are sending samples in duplicate or triplicate, it is helpful for us for them to be grouped together.
  • Solid samples must be dry and powdered.
  • Make sure lids are air-tight for all vials or bottles.
  • Filters may be wrapped in aluminum foil, or put into wide-mouth vials (eg scintillation vials).
How much material do I weigh for CN analysis?

General Rule:

Since the %C is almost always larger than the %N, it is usually the %N that determines the amount of material to weigh.

In general, the equation 10 ÷ %N will give you the mg of material to weigh, targeting 100µg of N.

If that amount is larger than about 200 mg, it would be better to use 5 ÷ %N. We can even do 3 ÷ %N if needed.

If you have groups of material with quite different C:N ratios, it is best to put them in different submission files. Contact us if you need help deciding.

You must always include the %N and %C data in the submission forms, as well as the weights. We need to know the C:N in order to determine the dilution setting to use for the 13C analysis.

When the C:N is about 50:1, up to about 75:1:

Please contact someone at the lab to verify the amount of material you should weigh. At this point, a compromise is needed. We reduce the normal target of 100µg of N in order to also reduce the extremely high amount of C.

When the C:N is about 75:1 or more:

At this point it is strongly recommended to run for 15N and 13C in separate runs. The compromise is too great to get good data in a single run.

When running for 15N, we will use a CO2 trap to prevent the large slug of CO2 generated in the EA from reaching the IRMS.

The rules above still apply to the weights needed for 15N.

When running for 13C only:

A target of 300µg of C is optimal. (i.e. 30 ÷ %C). The general rule above applies to C in this case as well.  We can use less material if needed, please contact us.

How to prepare waters for dic/doc or tic/toc analysis.


  • Mandatory use of 40mL pre-cleaned borosilicate EPA vials with septa caps, purchased from a major laboratory supplier; quality assurance grade is not necessary (e.g. Fisher # 05-719-102UC; 72/cs). Please order your EPA vials early; they are often back-ordered.
    NOTE: Please do not send 60 ml EPA vials. They do not fit into the carousel.
EPA vials for TICTOC analysis.

Number of replicate vials needed per sample:

  • Concentration (ppmC) only (no isotope analysis):
    • DIC/DOC = 2 identical vials per sample, filtered, full (no bubble or headspace) with extra septum
    • TIC/TOC = 2 identical vials per sample, full (no bubble or headspace) with extra septum
  • Inorganic C isotope analysis:
    • 13C (DIC) only = 2 identical full vials filtered (no bubble or headspace) with extra septum
    • 13C (TIC) only = 2 identical full vials (no bubble or headspace) with extra septum
  • Organic C isotope analysis:
    • 13C (DOC) only = 2 identical vials filtered, no extra septum. Very small headspace is ok; none is best.
    • 13C (TOC) only = 2 identical vials, no extra septum. Very small head space is ok; none is best.
  • Both Inorganic & Organic C isotope analysis:
    • 13C (DIC&DOC) = 3 identical full vials, filtered (no bubble or head space) with extra septum.
    • 13C (TIC&TOC) = 3 identical full vials, (no bubble or head space) with extra septum.
    • We can work with only two vials if absolutely necessary.
  • Both dissolved & total C analysis:
    • Samples for dissolved C are considered distinct from samples for total C.
    • Thus, we need the numbers of vials for each type as listed above.
    • List the dissolved samples and total samples separately in each submission file (eg. 1-dissolved, 2-dissolved, 3-dissolved, ..., 1-total, 2-total, 3-total, ...).
    • As above, only one media code per submission fie (organic vs. inorganic).
    • Note:  when requesting 13C, you get a concentration measurement as a bonus.  We still need an approximate concentration before running for 13C though.

Extra septum:

  • Samples for DIC or TIC require an extra septum (PTFE-rubber, see info below) inserted between the top of the vial and the cap. The silicone/Teflon septum provided with the EPA vials allow inorganic carbon to diffuse out unless the extra septum is used.
  • We now advise that you put the darker PTFE side against the water. The rubber side of the septum can potentially affect the organic carbon. (A. Parkes (2016) verbal communication).
  • The extra septum is not required for DOC or TOC; however if inorganic & organic carbon are requested, please submit three identical full vials with extra septum (if re-running for DIC/TIC we must use a fresh vial).
Extra septa for inorganic C analysis.

Chromatorgraphic Specialties
Part No. C8850522C
PTFE-rubber, 22mm flexseal disc


  • In addition to your personal label on the vial, please label each sample cap from 1 to xx in the same order as listed in the submission file. This helps us to quickly locate samples.
  • Each set of identical vials should have the same number on the cap. Replicate vials should have the same number on the cap. Only enter this sample once in the submission file.
  • Please include the number of replicate vials per sample directly in the submission file in either the comments box or comments column.
  • DO NOT use multiple layers of tape on the vial body as the vials will not fit into the carousel.... if you do, we will have to remove it all and it will make us very cranky! ;)
    Numeric labelling of vial caps


  • ONLY samples for DIC or DOC should be carefully and gently filtered to 0.45 µm or less.
  • Samples for TIC or TOC should NOT be filtered so that both dissolved and particulate C can be analysed.
  • NOTE: A filtered and an unfiltered version of the same sample water are considered two separate samples.


  • If you suspect that some of your dissolved organic matter (DOC) may have precipitated after filtration, it is possible for us to add a stir bar to the vial before analysis; however, this will incur an extra cost of $5 per sample.

Range of measurement:

  • We can analyse water samples ranging from about 0.5 to 80 ppm of carbon.
  • The machine used for fresh water and saline DIC/TIC allows us to select a variable volume of sample according to the expected concentration; therefore, the importance of providing us with all pertinent concentration info.
  • Please note: organic C and inorganic C concentrations can be vastly different. We end up having to re-run samples with varying volumes in order to be able to target each one separately.

Preservation agents:

  • Samples should remain refrigerated after sampling and kept cool but not frozen during shipping. Vials will be transferred to our refrigerator upon arrival.
  • If the samples are refrigerated and can be analysed quickly (a BIG if) it is preferable to not poison the waters for preservation. We do understand that in some cases it is necessary.
  • If the waters are poisoned, it MUST be clearly stated in the submission file; include the type of poison and amount.
  • IF submitting only for DOC/TOC (isotopes and/or conc.) you may just add acid (HCl or phosphoric), but you MUST keep the pH > 2; aim for 2-3.

"Abnormal" water samples:

  • "Normal" samples are considered to be freshwater lake, river, groundwater, or regular seawater samples that have organic and inorganic C concentrations of less than 80 ppm.
  • If your samples are out of the ordinary in any way (i.e. very high C concentrations, high salinity, organic contamination, very high or low pH, etc.), please contact us. We will let you know if we can analyse them. Our instrumentation is not adapted to handle extreme samples. Deep groundwaters tend to be problematic. If accepted, your high salinity and/or high concentration samples can be diluted with deionised water for an extra charge.
  • If your sample concentrations are below our minimum (0.5 ppm) there is nothing to be done; no isotopic data will be possible.

Submission files

  • Only 1 media code per submission file (DIC/TIC or DOC/TOC or ppmC-only); each requires a separate file.
  • Submit a file for concentration (ppmC; media code 40) only if you are NOT submitting for isotopes.
  • List each sample only once.
  • Include the number of replicate vials per sample in the Comments box at the top if the same for all, or in the Comments column if variable.
  • Describe the type of waters you are submitting (e.g. lake, river, pond, ice meltwater, sea water, brines, groundwater, sediment porewater etc.).
  • Include the pH & salinity data for each sample if you have it; otherwise, give an estimate.
  • Include the DIC/TIC and/or DOC/TOC concentrations (ppmC or mg/L) of each sample if you have the data; otherwise, provide an estimate (helps enormously in estimating sample volume to use in analysis).
  • If submitting for DOC only, please include a DIC concentration estimate as well, as we may need to sparge the samples (acidification and removal of DIC) prior to analysis.
  • If a preservation agent was used, include the type of agent (e.g. HgCl2, HCl, etc) and the amount used in the general comments box.
  • PLEASE REPEAT within your email message the number of samples that you are sending as well as the type of analysis that you wish done, for verification purposes.


  • NEVER EVER ship vials glass on glass. They WILL break.
  • See sample submission (shipping) for more details.
Why do I need to worry about carbonates in my sediments or soils?
  • Analysis of sediments or soils analysed for carbon is a bulk method.  The EA cannot distinguish between inorganic and organic carbon.
  • Even a very small amount of carbonate-C can change the organic carbon 13C signature. See table below.
Relative % inorganic C
 where 13Cinorg @ -5‰
Combined Delta
where 13Corg @ -25‰

Effect of
(shift in C-org)

Total %C
50% -15.0‰ 10.0‰ 6.0 Really?!
10% -23.0‰ 2.0‰ 4.4 Not great
5% -24.0‰ 1.0‰ 4.2 Ballpark; in a rush.
2.5% -24.5‰ 0.5‰ 4.1 Definite small effect
1% -24.8‰ 0.2‰ 4.04 Ok, maybe
0% -25.0‰ 0.0‰


Yes. Real value!


What method should I use to remove carbonates from soils or sediments?
  • There is no perfect method.
  • First you need to determine the type(s) of carbonate(s) present in your soil or sediment.  Calcite is easy to remove; dolomite is possible to remove with more work.  Anything more durable is extremely difficult to remove.
  • Do a literature search to see what method others in your field have used.  Make your choice based on this information, and on the type(s) of carbonate(s) present.
  • Make sure to retain some untreated material to use for N analysis if desired; any treatment of the sediment or soil can affect the nitrogen signature.  We strongly recommend running the N and C isotopes separately for best results.
Convert Delta to ATM%
Absolute Ratios (AR) of mole fractions.
Isotope Standard Absolute Ratio (AR)
C13 VPDB 0.0111803 *
N15 AIR 0.0036764 **
D VSMOW 0.0001557 **
O18 VSMOW 0.0020051 **
O17 VSMOW 0.000379 **

* Berglund, M. and Weiser, M. (2011) Isotopic Composition of the Elements 2009 (IUPAC Technical Report), Pure Appl. Chem., Vol. 83, No. 2, pp. 397–410

** Compilation of Minimum and Maximum Isotope Ratios of Selected Elements in Naturally Occurring Terrestrial Materials and Reagents, U.S. Geological Survey Water-Resources Investigations Report 01-4222 (Revised June 2002).

atm% = (100 * AR * (Delta/1000 + 1)) / (1 + (AR * (Delta/1000 + 1)))

Where AR is the Absolute Ratio (constant) and Delta is the value in permil to be converted into atm %.

Click to download an Excel conversion calculator.

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