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Primary production in Cariaco, microbial biomass, and midwater dark CO2 fixation vary strongly with factors such as seasonal riverine inputs, seasonal upwelling intensity, lateral intrusions of water from the Caribbean Sea, and trade-wind intensity [ 22- 24].
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While the total number of fixations was determined by syntax, the duration of each fixation varied with the complexity of the arithmetic operation at each step.
The rate of rearrangement fixation varies significantly within and between animal groups [ 2, 5].
The postmortem time before fixation varied from 12 to 36 hours.
The type of stem fixation varied, with the majority being cemented stems giving hybrid revision THA.
However, there were several areas where the amplitude of the category preference (tool pictures vs fixation – animal pictures vs fixation), varied linearly with age.
To illustrate how the additive effect on the probability of revision of type of fixation varied with time, we prepared a graph based on the semi-parametric additive model showing the difference in the cumulative subdistribution hazard rates of revision for cementless vs. cemented fixation of the prostheses.
The dichotomized covariate age group showed an effect on rate and probability of revision that varied with time; however, we chose to model it as constant, as the effect on the other covariates was negligible and the main interest was how the effect of fixation varied with time.
The postmortem interval preceding fixations varied, but in most cases the brains were immersed in cold (4°C) 4% paraformaldehyde in 0.1 M phosphate buffer (pH 7.4) for less than 30 minutes after removal from the uterus.
The classification problem at hand is a challenging one, for several reasons: (i) the mutational process is a completely random one; only the rate of fixation varies between functional and non-functional sites.
In addition, N2 fixation rates may differ over seasons (Lett and Michelsen 2014) and thus the microbial guilds actively performing N2 fixation may vary with season.
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