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Growth on individual substrate was removed periodically to assess the concentration of following changes in optical density at 600 nm of washed cells against biotic (without a substrate) and sterile (without bacteria) controls and tested for its bioremediation capacity in situ mesocosm to degrade multiple substrates after 12-day incubation period.
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(A), Abiotic system without biosurfactant at T = 0 days (B), Abiotic system without biosurfactant at T = 20 days (C), Biotic system without biosurfactant at T = 20 days (D), Biotic system with biosurfactant at T = 20 days.
Available data still suggest that it should be possible to improve resistance to biotic stress without negatively affecting abiotic stress resistance.
As shown in Table 1 the biotic system without biosurfactant depicted a wide range of demonstrable n-alkanes degradation 6-1000%), whereas iso-alkanes showed some degree of recalcitrance in relation to linear hydrocarbons 14-311%).
First, the plants without ants in observational studies may have been without their biotic defenders for a long period (longer than the duration of the ant removal experiments), and therefore suffered greater long-term negative effects from herbivory.
Progress has been made in reconstructing genomes of uncultivated viruses de novo, from biotic and abiotic environments, without laboratory isolation of the virus host system.
Local adaptation was prominent when comparing performance on hosts with an AMF treatment and a control treatment without introduced biotic component, and tendentious when mites were selected on plants with belowground nematode herbivory.
The hypothesis of these species reaching the extent of the fundamental niche (i.e., sites of suitable habitat without considering biotic interactions) in the contiguous US, could be corroborated with climate-matching (e.g., [4]) and niche-modeling [3], which incorporate information on native population environmental tolerance.
Spatial neighbourhoods in species occurrence data have been included in SDM models of single species (without considering biotic interactions) (Augustin, Mugglestone & Buckland, 1996).
However, such an interaction seems unlikely for monocots (these plants act as hosts to few viruses), members of which accumulate miR168 at higher levels even without any biotic stress.
This was likely due to mechanisms that have evolved to protect plants against biotic and abiotic stresses without severe morphological changes, particularly to help plants to respond to mild environmental changes.
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