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Exploiting the higher temperature roots of existing geothermal systems could result in increased productivity and sustainability.
Because of the technical challenges associated with drilling deeper into the higher temperature roots of hydrothermal systems, few wells have encountered supercritical (T > 374 °C, P > 221 bar for pure water, T > 406 °C, P > 298 bar for seawater) conditions.
After an overnight incubation at room temperature, roots were washed with deionized water and analyzed by CLSM.
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The temperature root mean square error of indoor air is lowered to below 0.5 K in both summer and winter.
Growth under optimal environmental conditions (e.g. air temperature, root-zone water storage) is described by either a power or sigmoidal function (see Kimberley and Richardson, [2004] for a range of functional forms).
Differences in soil temperature, root length, root surface area, root biomass, shoot biomass, and root:shoot biomass ratio were determined by two-way ANOVA with media and watering treatment as fixed factors and with P < 0.05 indicating significance.
Given the potential differences in pine seedling growth in traditionally used organic media in the greenhouse vs. native mineral soils under drought conditions, we investigated the influences of growth medium and drought on soil surface temperature, root architecture, and biomass accumulation in ponderosa pine seedlings.
The reconstructed steady-state temperatures agreed with the measured temperatures; root-mean-square error ranged from 0.45 to 1.21 degrees C. The transient three-dimensional tumour temperature was estimated assuming that the perfusion was constant throughout the treatment.
Surface energy balance equations were used to estimate soil surface temperature, and root growth and root distribution models were incorporated to represent the special contribution of plant roots in the vegetated soils.
Plates were wrapped with Micropore tape and incubated in the dark at room temperature until roots emerged, usually in around 3 weeks.
In contrast, BTF3 transcript level was significantly increased by salt stress in Suaeda asparagoides [ 31], while expression level of SabBTF3 was differentially regulated by various abiotic stresses, such as drought, salinity, ABA, and temperature in roots [ 7].
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