A modified Coulomb's law for the tangential debonding of osseointegrated implants.

Cementless implants are widely used in orthopedic and dental surgery. However, debonding-related failure still occurs at the bone-implant interface. It remains difficult to predict such implant failure since the underlying osseointegration phenomena are still poorly understood. Especially in terms of friction and adhesion at the macroscale, there is a lack of data and reliable models. The aim of this work was to present a new friction formulation that can model the tangential contact behavior between osseointegrated implants and bone tissue, with focus on debonding. The classical Coulomb's law is combined with a state variable friction law to model a displacement-dependent friction coefficient. A smooth state function, based on the sliding distance, is used to model implant debonding. The formulation is implemented in a 3D nonlinear finite element framework, and it is calibrated with experimental data and compared to an analytical model for mode III cleavage of a coin-shaped, titanium implant (Mathieu et al. in J Mech Behav Biomed Mater 8(1):194-203, 2012). Overall, the results show a close agreement with the experimental data, especially the peak and the softening part of the torque curve with a relative error of less than 2.25%. In addition, better estimates of the bone's shear modulus and the adhesion energy are obtained. The proposed model is particularly suitable to account for partial osseointegration.

Evaluation of gamma contribution in a neutron calibration field of Am-Be241 source.

The paper presents the evaluation of gamma contribution in a neutron calibration field of a 241Am-Be source. The characterization of gamma flux spectra and gamma ambient dose equivalent rates has been performed using a portable NaI(Tl) gamma spectrometer. For obtaining the gamma ambient dose equivalent rates from the measured spectra, two approaches were applied based on the applications of the G(E) function and the ICRP 74 conversion factors, respectively. Comparison of the gamma ambient dose equivalent rates obtained from the two approaches shows an agreement within 5%. The gamma contribution in the neutron calibration field is evaluated about 2.3-3.3% of the total neutron ambient dose equivalent rate in the distance range of 100-250cm.

A projection method to extract biological membrane models from 3D material models.

This paper presents a projection method for deriving membrane models from the corresponding three-dimensional material models. As a particular example the anisotropic Holzapfel-Gasser-Ogden model is considered. The projection procedure is based on the kinematical and constitutive assumptions of a general membrane theory, considering the membrane to be a general two-dimensional manifold. By assuming zero transverse stress, the Lagrange multiplier associated with the incompressibility constraint can be eliminated from the formulation. The resulting nonlinear model is discretized and linearized within the finite element method. Several numerical examples are shown, considering quadratic Lagrange and NURBS finite elements. These show that the proposed model is in very good agreement with analytical solutions and with full 3D finite element computations.

Adaptation changes stereoscopic depth selectivity in visual cortex.

Exposure to specific visual stimuli causes a reduction in sensitivity to similar subsequent stimulation. This adaptation effect is observed behaviorally and for neurons in the primary visual cortex. Here, we explore the effects of adaptation on neurons that encode binocular depth discrimination in the cat's primary visual cortex. Our results show that neuronal preference for binocular depth is altered selectively with appropriate adaptation. At the preferred depth, adaptation causes substantial suppression of subsequent responses. Near the preferred depth, the same procedure causes a shift in depth preference. At the null depth, adaptation has little effect on binocular depth coding. These results demonstrate that prior exposure can change the depth selectivity of binocular neurons. The findings are relevant to the theoretical treatment of binocular depth processing. Specifically, the prevailing notion of binocular depth encoding based on the energy model requires modification.

Contrast sensitivity is enhanced by expansive nonlinear processing in the lateral geniculate nucleus.

The firing rates of neurons in the central visual pathway vary with stimulus strength, but not necessarily in a linear manner. In the contrast domain, the neural response function for cells in the primary visual cortex is characterized by expansive and compressive nonlinearities at low and high contrasts, respectively. A compressive nonlinearity at high contrast is also found for early visual pathway neurons in the lateral geniculate nucleus (LGN). This mechanism affects processing in the visual cortex. A fundamentally related issue is the possibility of an expansive nonlinearity at low contrast in LGN. To examine this possibility, we have obtained contrast-response data for a population of LGN neurons. We find for most cells that the best-fit function requires an expansive component. Additionally, we have measured the responses of LGN neurons to m-sequence white noise and examined the static relationship between a linear prediction and actual spike rate. We find that this static relationship is well fit by an expansive nonlinear power law with average exponent of 1.58. These results demonstrate that neurons in early visual pathways exhibit expansive nonlinear responses at low contrasts. Although this thalamic expansive nonlinearity has been largely ignored in models of early visual processing, it may have important consequences because it potentially affects the interpretation of a variety of visual functions.

Transcranial magnetic stimulation elicits coupled neural and hemodynamic consequences.

Transcranial magnetic stimulation (TMS) is an increasingly common technique used to selectively modify neural processing. However, application of TMS is limited by uncertainty concerning its physiological effects. We applied TMS to the cat visual cortex and evaluated the neural and hemodynamic consequences. Short TMS pulse trains elicited initial activation (approximately 1 minute) and prolonged suppression (5 to 10 minutes) of neural responses. Furthermore, TMS disrupted the temporal structure of activity by altering phase relationships between neural signals. Despite the complexity of this response, neural changes were faithfully reflected in hemodynamic signals; quantitative coupling was present over a range of stimulation parameters. These results demonstrate long-lasting neural responses to TMS and support the use of hemodynamic-based neuroimaging to effectively monitor these changes over time.

Spatial frequency-specific contrast adaptation originates in the primary visual cortex.

Adaptation to a high-contrast grating stimulus causes reduced sensitivity to subsequent presentation of a visual stimulus with similar spatial characteristics. This behavioral finding has been attributed by neurophysiological studies to processes within the visual cortex. However, some evidence indicates that contrast adaptation phenomena are also found in early visual pathways. Adaptation effects have been reported in retina and lateral geniculation nucleus (LGN). It is possible that these early pathways could be the physiological origin of the cortical adaptation effect. To study this, we recorded from single neurons in the cat's LGN. We find that contrast adaptation in the LGN, unlike that in the visual cortex, is not spatial frequency specific, i.e., adaptation effects apply to a broad range of spatial frequencies. In addition, aside from the amplitude attenuation, the shape of spatial frequency tuning curves of LGN cells is not affected by contrast adaptation. Again, these findings are unlike those found for cells in the visual cortex. Together, these results demonstrate that pattern specific contrast adaptation is a cortical process.

Origins of cross-orientation suppression in the visual cortex.

The response of a neuron in striate cortex to an optimally oriented stimulus is suppressed by a superimposed orthogonal stimulus. The neural mechanism underlying this cross-orientation suppression (COS) may arise from intracortical or subcortical processes or from both. Recent studies of the temporal frequency and adaptation properties of COS suggest that depression at thalamo-cortical synapses may be the principal mechanism. To examine the possible role of synaptic depression in relation to COS, we measured the recovery time course of COS. We find it too rapid to be explained by synaptic depression. We also studied potential subcortical processes by measuring single cell contrast response functions for a population of LGN neurons. In general, contrast saturation is a consistent property of LGN neurons. Combined with rectifying nonlinearities in the LGN and spike threshold nonlinearities in visual cortex, contrast saturation in the LGN can account for most of the COS that is observed in the visual cortex.

Cross-orientation suppression: monoptic and dichoptic mechanisms are different.

The response of a cell in the primary visual cortex to an optimally oriented grating is suppressed by a superimposed orthogonal grating. This cross-orientation suppression (COS) is exhibited when the orthogonal and optimal stimuli are presented to the same eye (monoptically) or to different eyes (dichoptically). A recent study suggested that monoptic COS arises from subcortical processes; however, the mechanisms underlying dichoptic COS were not addressed. We have compared the temporal frequency tuning and stimulus adaptation properties of monoptic and dichoptic COS. We found that dichoptic COS is best elicited with lower temporal frequencies and is substantially reduced after prolonged adaptation to a mask grating. In contrast, monoptic COS is more pronounced with mask gratings at much higher temporal frequencies and is less prone to stimulus adaptation. These results suggest that monoptic COS is mediated by subcortical mechanisms, whereas intracortical inhibition is the mechanism for dichoptic COS.