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Tseng, C.-C.

Publications and source records attributed to Tseng, C.-C..

2 recordsLinked to original sources

The Fallacy and Bias of Averages on Vegetation Indices based Plant Phenotyping

BackgroundVegetation indices (VIs) from remote sensing are widely used for non-destructive plant phenotyping, often averaged across plots or image regions to represent each plot. However, according to Jensens inequality, which is known as the "fallacy of the average", it can bias estimates when nonlinear relationships exist between VIs and target traits. To examine this issue, we systematically assessed the severity of this bias and tested a correction method. VI values were simulated using six beta distributions with varying shapes and skewness, and with normalized difference vegetation index (NDVI) images from a paddy rice experiment to evaluate bias under real conditions. Nonlinear link functions (concave, convex, logistic) with different noise levels were applied to model VI-trait relationships. ResultThe results showed that averaging under nonlinear relationships reduced predictive performance, lowering the coefficient of determination (R2) between true and predicted traits by up to 82%. In the rice NDVI simulation, R2 was reduced by up to 58% around the tillering stage. Our correction method, which predicts traits from VI before averaging, substantially mitigated bias, improving R2 by up to 0.68 depending on noise level, VI distribution, and link function. To facilitate application, we established an interactive R Shiny website enabling users to quantify potential biases and the efficacy of corrections within this workflow based on their own research conditions ConclusionIn summary, averaging VIs without accounting for nonlinear relationships can introduce substantial bias and degrade phenotyping accuracy. This bias should be explicitly considered in phenotyping analyses, and correction methods applied when appropriate to improve reliability.

plant biology↗

Gap junctions in Turing-type periodic feather pattern formation

Periodic patterning requires coordinated cell-cell interactions at the tissue level. Turing showed, using mathematical modeling, how spatial patterns could arise from the reactions of a diffusive activator-inhibitor pair in an initially homogenous two-dimensional field. Most activators and inhibitors studied in biological systems are proteins, and the roles of cell-cell interaction, ions, bioelectricity, etc. are only now being identified. Gap junctions (GJs) mediate direct exchanges of ions or small molecules between cells, enabling rapid long-distance communications in a cell collective. They are therefore good candidates for propagating non-protein-based patterning signals that may act according to the Turing principles. Here, we explore the possible roles of GJs in Turing-type patterning using feather pattern formation as a model. We found seven of the twelve investigated GJ isoforms are highly dynamically expressed in the developing chicken skin. In ovo functional perturbations of the GJ isoform, connexin 30, by siRNA and the dominant-negative mutant applied before placode development led to disrupted primary feather bud formation, including patches of smooth skin and buds of irregular sizes. Later, after the primary feather arrays were laid out, inhibition of gap junctional intercellular communication in the ex vivo skin explant culture allowed the emergence of new feather buds in temporal waves at specific spatial locations relative to the existing primary buds. The results suggest that gap junctional communication may facilitate the propagation of long-distance inhibitory signals. Thus, the removal of GJ activity would enable the emergence of new feather buds if the local environment is competent and the threshold to form buds is reached. We propose Turing-based computational simulations that can predict the appearance of these ectopic bud waves. Our models demonstrate how a Turing activator-inhibitor system can continue to generate patterns in the competent morphogenetic field when the level of intercellular communication at the tissue scale is modulated.

developmental biology↗