Valid PointWhy Should Zero Point Be Excluded from Calibration Curves?

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Discussion Overview

The discussion revolves around the inclusion of the zero point (0,0) in calibration curves, particularly in the context of chemical analysis and instrument calibration. Participants explore the implications of including this point on the accuracy and validity of calibration, touching on concepts such as linearity, precision, and the behavior of different instruments.

Discussion Character

  • Debate/contested
  • Technical explanation
  • Conceptual clarification

Main Points Raised

  • One participant argues that including the zero point can lead to false precision, as it implies the ability to accurately measure values between zero and the next calibration point, which may not be valid.
  • Concerns are raised about the non-linear behavior of reactions at low and high concentrations, suggesting that the zero point may not accurately reflect instrument sensitivity or response.
  • Another participant mentions that multipoint calibration is intended to confirm linearity and correct for y-intercepts, questioning the validity of assuming the point (0,0) is accurate without data support.
  • One participant notes that the inclusion of the zero point can decrease the y-intercept and increase the slope of the calibration line, potentially leading to greater errors at the extremes of the calibration curve.
  • Another participant agrees that unless a device can be calibrated to return a value of zero, including it as a calibration point may not be appropriate.
  • One participant shares their experience of not including zero in calibration curves, emphasizing the importance of dynamic range and the potential irrelevance of points near the origin due to deviations from linearity.

Areas of Agreement / Disagreement

Participants express differing views on the inclusion of the zero point in calibration curves. While some argue against its inclusion due to concerns about precision and linearity, others suggest that its validity may depend on the specific instrument and context. The discussion remains unresolved with multiple competing perspectives.

Contextual Notes

Participants highlight limitations related to instrument sensitivity, the behavior of calibration curves at low and high concentrations, and the potential for deviations from linearity. These factors contribute to the complexity of deciding whether to include the zero point in calibration curves.

ShawnD
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I keep getting into arguments with my teachers about including zero as a point on my calibration curves. Their reasoning is that it should theoretically be valid since you won't get a signal when you do nothing (sound reasoning). My argument is that if you plot it, it is usually an outlier, unless you specifically tell your instrument "this is zero", and that only seems to apply to spectroscopy instruments.

Precision
When you do a calibration curve, you are stating "I can accurately determine values that fall within this range", which is why you need to adjust your sample concentrations until their readings fall within your calibration curve. If I include a zero point, I'm saying I can solve for values that are between zero and whatever the next point is. If I have points on my graph for 0 and 1ppm, I am basically stating that my machine is capable of accurate readings to infinite orders of magnitude between 0 and 1. You don't have this same false precision between points like 1 and 2 because 1.000001, 1.1, and 2 are on the same order of magnitude.

Linearity
Reactions do not follow a linear trend through all points. This is especially true at very high and very low concentrations. Most reactions curve off or follow a lazy S shape. Curve-off at low concentrations is generally caused by a lack of instrument sensitivity. Curve-off at high concentrations is either caused by self-absorbance in spectroscopy, or exceeding the linear range of the detector itself for whatever the instrument may be. Lazy-S curves are usually due to logarithmic relations to concentration; cell potential for example. Nobody includes the high concentration curve-off points as part of their linear calibration curve, so why would anybody include the zero point which has all these low concentration linearity problems?

Why are we doing multipoint?
Multipoint calibration is done to confirm linearity as well as correct for y-intercepts. If you assume the point at 0,0 is valid, you've completely missed the boat on why you are doing this. Did you follow the data to see if it should intersect at 0,0? No, you lead the data by saying it's a valid point. That is not science. You do not lead the data like that, ever.

Invalid check standards
From what I've seen, the y-intercept for response vs concentration is usually positive. When the zero point is part of the calibration, it typically decreases the y-intercept and increases the slope (think of rotating the best fit line counterclockwise). This keeps the best fit line in a similar position for the middle part of the calibration, but it greatly increases the errors at low and high ends of the calibration curve. Since your check standard is usually somewhere near the middle calibration point, your check standard will be ok, but whatever you are analyzing may fall closer to the ends of the calibration, and the resulting error is enormous for seemingly no reasaon. I've had this happen to me many times before. Each time I go back, remove the zero point, and redo the calculations, both the check standard and sample being analyzed are closer to what they should be.



In conclusion, including the point 0,0 should almot never be done.
 
Last edited:
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'Tain't clear what your question is: sensitivity, dynamic range, absolute uncertainty, percentage uncertainty, and response function look to have been all mixed together --- not necessarily by you, but somewhere in your education.

0,0? Sure. All the time in thermocouple calibrations; one variable isn't strictly 0. Chemistry and "0,0"? It's a logarithmic universe, so you've got zero log values showing up all the time, but no zeroes. Physical chemistry and 0,0? "log of this vs. one over that?" Same game.

Help?
 
Seems to me that unless the device can be actually calibrated to return a value of zero when you zero it (some do, some don't), you shouldn't use it as a calibration point because, like you said, it gives a false precision.

But it would depend on the device.
 
From the labs that I've done so far, I haven't included zero in the calibration curves, what you're concerned is with the dynamic range of the data and as long as you have subtracted off a background, the zero is somewhat irrelevant, unless the curve is a special plot where the intercept is supposed to represent a parameter. In fact, with beer's law, I think you get some deviation from linearity at the extreme ends of the plots, better or worse depending on the instrumentation, techniques, and the conditions employed, it's important to realize that the points near the origin may not even be realistic, and "off the mark", irrelevant.
 
ShawnD said:
In conclusion, including the point 0,0 should almot never be done.
Haven't read the entire post, but I agree with that last bit based on definition : The calibration curve is (the suitably smoothed) the two-column data generated during an experimental run.

Extrapolation is a crime punishable by death (or grad school) ! :biggrin:
 

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