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Regardless of observer reliability, the matrix method produced substantial overestimates of the population size when surveying effort was low.
At sampling efforts around 0.26% of the study area (thirteen kilometers of transect in this study, or 0.26 km2), both the marked recount method and the matrix method produced results of reasonable accuracy and precision.
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Being based on a Vandermonde decomposition of the prediction matrix, the matrix pencil method produces biased estimates when applied directly to data of the constant-Q model.
This method produced electrodes composed of Fe3C nanoparticles embedded in a matrix of disordered nanocrystalline carbon with predominantly fibrous morphology.
An agglomeration of Al2O3 nanoparticles was not explicitly observed, implying that the processing method produced a reasonably uniform distribution of the nanoparticles in the matrix of the composites.
At sampling efforts below this level, neither method produced accurate or precise results: the marked recount method tended to produce underestimates while the matrix method tended to produce overestimates, and the range of estimates returned were very wide for both methods.
The proposed method produces a simple matrix expression for the deflection of the beam.
In this work, it is demonstrated that a novel in-situ synthesis of SiO2 nanoparticles in DES can effectively improve the distribution uniformity of SiO2 nanoparticles in the Ni matrix compared with the conventional addition method, producing a homogenous Ni/SiO2 nanocomposite coating.
However, this method produces an unsymmetrical interpolation matrix.
However, since the PWL method produces a symmetric positive-definite coefficient matrix, it should be substantially more computationally efficient than Palmer's method, which produces an asymmetric matrix.
These investigations on the interactions between three matrices and three DNA extraction methods produced no evidence to support any relation between UV light absorbance ratios and inhibition run-based assessment of the quality of DNA extracts for target analyte quantification by RT-PCR technology.
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