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The multiple components at approximately 1690 1660 cm−1 possibly reflect interactions of parchment with ink components.
We used the east west (EW), north south (NS), and up down (UD) components at approximately 400 GPS sites in the Tokai, Kanto, and Tohoku regions.
The main output in the mid-visible range is comprised of two components at approximately 506 and 564 nm, and is attributed to transitions involving oxygen defects, specifically the bulk-related VO+→VB transition for the 506-nm emission and depletion region-related CB→VO++ transition for the 564-nm emission.
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Swarm observes comparable peaks in the cross-track component at approximately the same locations as the statistical model, but the peaks are much narrower and the surrounding flow is considerably offset from the statistical model.
The NS anisotropy is smallest in NM data at approximately 17 GV and largest in the GG-component at approximately 80 GV, with the anisotropy in the GMDN at approximately 60 GV in between, suggesting that the NS anisotropy increases with increasing rigidity (Munakata et al. 2014).
Evidence is considered that indicates that surface oxygen is connected with the red emission peak at 643 nm, while the possibility is flagged of a small yellow-orange component at approximately 580 nm connected with the presence of OH surface groups.
The characteristic morphology of ERPs from occipito-lateral sites was observed at a post stimulus latency of approximately 100 200 ms. In this time range, the waveforms obtained from the three midline electrode sites displayed a large positive valley, while the occipito-temporal electrodes exhibited a W-shaped pattern with a central negative component at approximately 140 ms latency.
The Raman spectrum (Fig. 2b, middle trace) corroborates the β-sheet assignment with the appearance of a high frequency Amide I component at about 1,669 cm−1 and a strong Amide III component at approximately 1,240 cm−1.
Finally, in the blend, the secondary relaxation processes of both components occur at approximately the same temperature-frequency location as those in corresponding neat polymers, but with much lower intensity, suggesting suppression by the intermolecular hydrogen bonding.
Finally, we measured the yield components at harvest (approximately 6 weeks after heading) (Table 2).
It is highly likely that the component identified at approximately 70 ms corresponds to our M70.
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