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An analysis of different process parameters allowed the evaluation of the applied fermentation process (fed-batch, Table 1: medium C) with earlier findings from cultivations in the original medium (batch, Table 1: medium B).
Owner status gave no apparent advantage in terms of exclusive oviposition because in 10 of the 15 observations, both owners and intruders oviposited into at least one egg within a batch (Table 2).
There is a possibility to measure how long it took the Cardholder to enter PIN code, place a signature, etc. Fig. 4 Example transactions' traces batch Table 1 Structure of single transaction's trace Pos.
Blanc and Goma (1987) obtained a productivity of 0.10 g L−1 h−1 for acetic acid while in the present work, the productivity of acetic acid decreased from 0.05 g L−1 h−1 in the first batch to 0.03 g L−1 h−1 in the third sequential batch (Table 4).
Such a structure of a batch's entry has a few advantages: (1) There is a possibility to measure how long it took the Cardholder to enter PIN code, place a signature, etc. Fig. 4 Example transactions' traces batch Table 1 Structure of single transaction's trace Pos.
The second measurements were made on the 2011 or 2012 batch (Table 1), less than 1 week after acetolysis in the laboratory.
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Molecule, substance, and batch tables reflect the organization of the chemical data presented before.
Instead of updating the parameters after every training examples (stochastic gradient descent) or updating the parameters once after all the training examples have been processed (batch gradient descent), this technique speeds up the training process as gradient of loss is averaged over each mini-batch (Table 1).
In support of the conclusions, metal/micronutrient determination of the fed maize silage batches (Table 1) confirmed correspondingly low concentrations of Co and of Na in the batches fed before and at the secondary acidification.
The specific cell growth rate remained at a constant value of 0.014 h−1 over the batches (Table 7; the definitions of the abbreviations used in Table 7 can be found in Table 1).
Moreover, the deviations were possibly derived from the worse accuracy for the excessively D-enriched ( {updelta mathrm{D}}_{{mathrm{H}}_2mathrm{O}} ) measurement resulting from the over range of calibration by using the commercial standards having relatively lower isotopic values (see Methods) than the ( {updelta mathrm{D}}_{{mathrm{H}}_2mathrm{O}} ) values of the experimental batches (Table 2).
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