2012
DOI: 10.2134/agronj2011.0100
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Geostatistical Models in Agricultural Field Experiments: Investigations Based on Uniformity Trials

Abstract: The probability of detecting treatment differences can often be increased by using geostatistical instead of classical statistical models. Geostatistical approaches require the selection of the best fitted model from a set of alternative models. This additional analysis effort could be reduced if the same model shows consistently the best fit for a given field or crop. To prove whether this reduction can be expected for designed on‐station trials, we analyzed five uniformity trials conducted on the same field.… Show more

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Cited by 14 publications
(19 citation statements)
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“…We found that under high Fig. Therefore, spatial modeling should be considered as a supplemental strategy rather than an alternative to experimental design, as was also suggested by Richter and Kroschewski (2012) and Piepho et al (2015). Recovery of the best genotypes (Best_Gen), Pearson's correlation coefficient between true and estimated genotypic effects (COR), and the SE of the difference between cultivar means (SED) for six experimental designs: completely randomized design (CRD), randomized complete block design (RCBD) incomplete blocks and a-lattice design with block size of 5 (ALPHA_5), incomplete blocks and a-lattice design with block size of 10 (ALPHA_10), partially replicated design with 200 genotypes (PREP g , this experiment preserved the number of genotypes and thus used fewer experimental units), and a partially replicated design with 428 genotypes (PREPn, this experiment preserved the number of experimental units and thus evaluated more genotypes).…”
Section: Discussionsupporting
confidence: 63%
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“…We found that under high Fig. Therefore, spatial modeling should be considered as a supplemental strategy rather than an alternative to experimental design, as was also suggested by Richter and Kroschewski (2012) and Piepho et al (2015). Recovery of the best genotypes (Best_Gen), Pearson's correlation coefficient between true and estimated genotypic effects (COR), and the SE of the difference between cultivar means (SED) for six experimental designs: completely randomized design (CRD), randomized complete block design (RCBD) incomplete blocks and a-lattice design with block size of 5 (ALPHA_5), incomplete blocks and a-lattice design with block size of 10 (ALPHA_10), partially replicated design with 200 genotypes (PREP g , this experiment preserved the number of genotypes and thus used fewer experimental units), and a partially replicated design with 428 genotypes (PREPn, this experiment preserved the number of experimental units and thus evaluated more genotypes).…”
Section: Discussionsupporting
confidence: 63%
“…On the other hand, spatial modeling did not outperform experimental design in any of our situations. Therefore, spatial modeling should be considered as a supplemental strategy rather than an alternative to experimental design, as was also suggested by Richter and Kroschewski (2012) and Piepho et al (2015). Under high field variability, CRD or RCBD with spatial corrections were similar to ALPHA without spatial correction for precision.…”
Section: Discussionmentioning
confidence: 91%
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“…For the randomized design, we used a new randomization for each window. Because the designs were superimposed onto uniformity trial data, the resulting trials simulated the global null hypothesis of no treatment differences (Richter and Kroschewski 2012). With proper randomization, the analytical P-values for the F-tests should be uniformly distributed.…”
Section: A Uniformity Trialmentioning
confidence: 99%
“…While the NNA indirectly uses covariates to model spatial variation, the CE models directly account for the spatial variation using covariance structures among residuals based on distance (isotropic models) and both distance and direction (anisotropic models) (Littell et al, 2006). Therefore, a spatial model that is adequate for one trial may not be adequate for other trials, hence comparison of different spatial models to determine the best plausible model for each trial is recommended (Gilmour et al, 1997;Richter and Kroschewski, 2012). Therefore, a spatial model that is adequate for one trial may not be adequate for other trials, hence comparison of different spatial models to determine the best plausible model for each trial is recommended (Gilmour et al, 1997;Richter and Kroschewski, 2012).…”
mentioning
confidence: 99%