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While the rippling amplitude varies appreciably, the rippling wavelength varies very little and can be estimated from simple mechanical considerations.
Results of the evaluation suggest that the fatigue strength of the bone/cement interface in cemented total joint replacements can be estimated from simple quasi-static shear tests.
The magnitude of this permeability can be estimated from simple scaling relationships.
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The dependence of the elastic constants on fiber volume fraction was estimated from simple mixture rules.
The extent of this degradation can be estimated from a simple argument: The lowest population frequency entering our estimator is of the order u/(sic), while drift-dominated haplotypes will typically be at frequencies t/ N, where t is the time that has elapsed since the sweep.
At minimized As flux, the hole depth d can be estimated from a simple scaling law [10]: d = c_{h} theta^{2/3} exp [- E_{h} / k_{B} T)] (1).
They further proposed that the value of this critical neutrophil concentration can be estimated from a simple linear mathematical model that is fitted to the experimental data.
With no reason to suspect gene flow between the two taxa, the expectation of shared polymorphisms can be estimated from the simple isolation model (IM) of speciation, as implemented in the WH program.
If the ratio Nb /Ne is known or can be estimated from two or three simple life history traits, Nb can be estimated with little (≤5 10%) bias.
We provide a quantitative bias correction for raw N ^ b based on the ratio Nb/ Ne, which can be estimated from two or three simple life history traits.
If this ratio is not known but can be estimated from two or three simple life history traits (Waples et al. 2013), modified adjustments to N ^ b are possible (Table 3).
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