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The energy proportion index is a possible indicator for the damage detection.
There was no obvious quadratic relationship of the hatchery-produced adult proportion index with hybrid smolt or adult proportions.
We used each of these indices individually and together as the hatchery-produced adult proportion index [hatchery index/(wild index + hatchery index)] as covariates in model selection analysis.
The best fit model predicting hatchery proportions included the hatchery-produced adult proportion index as the only covariate (Fig. 4, Tables 4 and S4).
Because the proportion of hybrids should increase only as the proportion of wild (or hatchery) spawners approaches 0.5 (a quadratic relationship), we analyzed one model for proportion of hybrids for each life history that included the hatchery-produced adult proportion index and a squared hatchery-produced adult proportion index.
Models run using the hatchery-produced adult proportion index generally had similar AIC c values as models run using the hatchery-produced adult number index for both smolt and adult datasets.
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However, change in the average speed index was small, in comparison with that of proportion indices, suggesting that the index of average speed had lower algorithm sensitivity.
The obtained indexes were split here in (1) robustness indexes, (2) morphofunctional indexes, and (3) proportion indexes to facilitate their interpretation.
As Samuels and Van Valkenburgh (2008)[33] previously showed, Manovas on robustness, morphofunctional and proportion indexes indicated a significant differentiation of the morphology within the dataset involving life-style (Wilk's Lambda test: Value = 0.00290, F = 78.265, p<0.001).
For each analysis, a set of 13 robustness, morphofunctional and proportion indexes was considered: SMI, BI, HRI, HEB, OLI, URI, CI, GI, FRI, FEB, TRI, TSI and IM (see Appendix S2 for definitions).
Given that the three limb proportion indices explain 86% of the variation in the differences between the DDM and CCNM estimates, the results of the regression analysis support the idea that the DDM yielded inaccurate estimates when applied to the fossil hominin sample because the latter included taxa with limb proportions that differ from those of humans.
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