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Standard deviation matrix

The superscript used in the coefficient matrices in (6.192) is a reminder that the statistics must be evaluated at the notional-particle location. For example, e = e(X r), and the scalar standard-deviation matrix and scalar correlation matrix p are computed from the location-conditioned scalar second moments X )(X, t). [Pg.316]

The reader is asked to find the standard deviations of the slopes matrix in Problem 9 below. [Pg.87]

Eind the standard deviations of the slopes in matrix (3-78) for row 2, which refers to absorbances measured at 525 nm. [Pg.91]

Measurement noise covariance matrix R The main problem with the instrumentation system was the randomness of the infrared absorption moisture eontent analyser. A number of measurements were taken from the analyser and eompared with samples taken simultaneously by work laboratory staff. The errors eould be approximated to a normal distribution with a standard deviation of 2.73%, or a varianee of 7.46. [Pg.295]

On the other hand, qy, is a measure of clay feed-rate variations, and a standard deviation of 0.3 tonnes/hour seemed appropriate. In the absence of any other information, standard deviations of the burner and dryer temperatures was also thought to be in the order of 0.3 °C. Thus, when these values are squared, the Q matrix becomes... [Pg.297]

To compute the variance, we first find the mean concentration for that component over all of the samples. We then subtract this mean value from the concentration value of this component for each sample and square this difference. We then sum all of these squares and divide by the degrees of freedom (number of samples minus 1). The square root of the variance is the standard deviation. We adjust the variance to unity by dividing the concentration value of this component for each sample by the standard deviation. Finally, if we do not wish mean-centered data, we add back the mean concentrations that were initially subtracted. Equations [Cl] and [C2] show this procedure algebraically for component, k, held in a column-wise data matrix. [Pg.175]

Figure 5.5. Summarized 6 C data Tor browsers and grazers, expressed as dark shaded and cross-hatched boxes, respectively, incorporating means and standard deviations, from the three groups of sites plotted against time (a) Die Kelders and Swartkrans, (b) Klasies and Makapansgat, and (c) Border Cave. Typical matrix values are shown as light shaded rectangles. Figure 5.5. Summarized 6 C data Tor browsers and grazers, expressed as dark shaded and cross-hatched boxes, respectively, incorporating means and standard deviations, from the three groups of sites plotted against time (a) Die Kelders and Swartkrans, (b) Klasies and Makapansgat, and (c) Border Cave. Typical matrix values are shown as light shaded rectangles.
For Klasies, although most values for both enamel and bone apatite fall within one standard deviation of the mean of (corrected) modem browser values (Fig. 5.5), some bone specimens fall outside this range. These enriched specimens suggest that a limited degree of equilibration with matrix carbonates has taken place, although inclusion of a limited amount of Q grass in the diet is a plausible alternative explanation for UCT 1025, Raphicerus sp. which as noted above could be the more opportunistic species, Raphicerus campestris. [Pg.105]

The uncertainties in the measurements (standard deviations) are placed in the diagonal matrix... [Pg.532]

The author gives an exampie of a study concerning a mixture of ethanol, toluene and ethyl acetate. The case is presented in the form of a Scheffe plan for which choice of compound quantities are not optimised to obtain a good matrix as shown in the matrix of effects correiation there is no point repetition in the middle of the matrix, which thus exciudes the quantification of the level of error of measurement that can only be estimated by the residual standard deviation of the regression. Finaliy, the author uses flashpoints of pure substances from partial experimental data. The available data give 9 to IS C for ethanol (the author 12.8), 2 to 9°C for toluene (5.56) and -4 to -2°C for ethyl acetate. [Pg.69]

To further analyze the relationships within descriptor space we performed a principle component analysis of the whole data matrix. Descriptors have been normalized before the analysis to have a mean of 0 and standard deviation of 1. The first two principal components explain 78% of variance within the data. The resultant loadings, which characterize contributions of the original descriptors to these principal components, are shown on Fig. 5.8. On the plot we can see that PSA, Hhed and Uhba are indeed closely grouped together. Calculated octanol-water partition coefficient CLOGP is located in the opposite corner of the property space. This analysis also demonstrates that CLOGP and PSA are the two parameters with... [Pg.122]

Scaling is a very important operation in multivariate data analysis and we will treat the issues of scaling and normalisation in much more detail in Chapter 31. It should be noted that scaling has no impact (except when the log transform is used) on the correlation coefficient and that the Mahalanobis distance is also scale-invariant because the C matrix contains covariance (related to correlation) and variances (related to standard deviation). [Pg.65]

Particularly for direct microanalytical techniques using <10 mg of sample for analysis, it is highly desirable to obtain quantitative information on element- and compound-specific homogeneity in the certificates for validation and quality control of measurements. As the mean concentration in a CRM is clearly material-related, the standard deviation of this mean value should represent the element s distribution in this matrix rather than differences in the analytical procedures used. [Pg.130]

Relative standard deviation of recoveries lower than 20% per representative matrix and fortification level... [Pg.26]

Method Pesticide Matrix ELOQ (mgkg ) LLMV (mg kg ) Av. recovery standard deviation Calc. MDL (mg kg ) Calc. MQL (mg kg ) Ref. [Pg.73]

Selectivity and sensitivity of available instruments are tested in all laboratories in the initial step of validation. The crops used for fortification experiments and the concentration levels are identical in all laboratories. Recoveries are determined with all available detection techniques, but after discussion of the results each laboratory selects individually one valid result for each analyte-matrix-level combination. Only this result is used for the calculation of the final mean recovery and standard deviation. Typical criteria for the acceptance of methods are given in Table 11. [Pg.125]

Optimizing the GC instrument is crucial for the quantitation of sulfentrazone and its metabolites. Before actual analysis, the temperatures, gas flow rates, and the glass insert liner should be optimized. The injection standards must have a low relative standard deviation (<15%) and the calibration standards must have a correlation coefficient of at least 0.99. Before injection of the analysis set, the column should be conditioned with a sample matrix. This can be done by injecting a matrix sample extract several times before the standard, repeating this conditioning until the injection standard gives a reproducible response and provides adequate sensitivity. [Pg.576]

Essentially this is equivalent to using (Sf/dk kj instead of (<3f/<3k,) for the sensitivity coefficients. By this transformation the sensitivity coefficients are normalized with respect to the parameters and hence, the covariance matrix calculated using Equation 12.4 yields the standard deviation of each parameter as a percentage of its current value. [Pg.190]

This schematic diagram shows that the true composition of particles can be obtained only when the probe hole covers the particle entirely. When the probe hole covers both the particle and the matrix, the measured concentration is lower than the real one. Again, when an interface is not perpendicular to the cylinder of analysis, the apparent concentration change at the interface appears diffuse, even if the real concentration change is discrete. The standard deviation for concentration, a, is given by... [Pg.8]


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