Angular dependence of metamagnetic transitions in DyAgSb2

Journals published by the American Physical Society can be found at http://journals.aps.org/Measurementsof the magnetization of DyAgSb2 reveal a complex system of up to 11 well-defined metamagnetic states for the field applied within the basal plane. Measurements of the magnetization vs the angle the applied field makes with respect to the [110] axis show the Dy3+ moments are constrained to lie along one of the four [110] directions within the basal plane. From the angular dependence of the critical fields and plateau magnetizations, the net distribution of the moments may be deduced for each state. Finally, the coupling constants are calculated within the framework of the "four-position clock model." [S0163-1829(99)04302-7]

Angular dependence of metamagnetic transitions in HoNi2B2C

Journals published by the American Physical Society can be found at http://journals.aps.org/Detailed measurements of M(2 K, H, theta) of HoNi2B2C, where theta is the angle that the applied field H makes with the [110] axis while remaining perpendicular to the crystallographic c axis, reveal three metamagnetic transitions with angular dependences H-c1 = (4.1 +/- 0.1 kG)/cos(theta), H-c2 = 8.4 +/- 0.2 kG/cos(phi), and H-c3 = (6.6 +/- 0.2 kG)/sin(phi), where phi = theta-45 is the angle from the [100] axis. The high-field saturated moment, M(sat) approximate to 10 mu(B)cos theta is consistent with the local moments being confined to the [110] direction. The locally saturated moments for fields between H-ci (i = 1, 2, 3) also manifest angular dependences that are consistent with combinations of local moments along [110] axes. Analysis of these data lead us to infer that the net distribution of moments is (up arrow down arrow up arrow down arrow up arrow down arrow) for H up arrow up arrow-->) for H-c2 up arrow up arrow-->) for H-c2 H-c3

Age-Dependent Ocular Dominance Plasticity in Adult Mice

Background: Short monocular deprivation (4 days) induces a shift in the ocular dominance of binocular neurons in the juvenile mouse visual cortex but is ineffective in adults. Recently, it has been shown that an ocular dominance shift can still be elicited in young adults (around 90 days of age) by longer periods of deprivation (7 days). Whether the same is true also for fully mature animals is not yet known. Methodology/Principal Findings: We therefore studied the effects of different periods of monocular deprivation (4, 7, 14 days) on ocular dominance in C57Bl/6 mice of different ages (25 days, 90–100 days, 109–158 days, 208–230 days) using optical imaging of intrinsic signals. In addition, we used a virtual optomotor system to monitor visual acuity of the open eye in the same animals during deprivation. We observed that ocular dominance plasticity after 7 days of monocular deprivation was pronounced in young adult mice (90–100 days) but significantly weaker already in the next age group (109–158 days). In animals older than 208 days, ocular dominance plasticity was absent even after 14 days of monocular deprivation. Visual acuity of the open eye increased in all age groups, but this interocular plasticity also declined with age, although to a much lesser degree than the optically detected ocular dominance shift. Conclusions/Significance: These data indicate that there is an age-dependence of both ocular dominance plasticity and the enhancement of vision after monocular deprivation in mice: ocular dominance plasticity in binocular visual cortex is mos

Loss of Arc renders the visual cortex impervious to the effects of sensory experience or deprivation

A myriad of mechanisms have been suggested to account for the full richness of visual cortical plasticity. We found that visual cortex lacking Arc is impervious to the effects of deprivation or experience. Using intrinsic signal imaging and chronic visually evoked potential recordings, we found that Arc−/− mice did not exhibit depression of deprived-eye responses or a shift in ocular dominance after brief monocular deprivation. Extended deprivation also failed to elicit a shift in ocular dominance or open-eye potentiation. Moreover, Arc−/− mice lacked stimulus-selective response potentiation. Although Arc−/− mice exhibited normal visual acuity, baseline ocular dominance was abnormal and resembled that observed after dark-rearing. These data suggest that Arc is required for the experience-dependent processes that normally establish and modify synaptic connections in visual cortex.Howard Hughes Medical InstituteNational Science Foundation (U.S.

Denoising Two-Photon Calcium Imaging Data

Two-photon calcium imaging is now an important tool for in vivo imaging of biological systems. By enabling neuronal population imaging with subcellular resolution, this modality offers an approach for gaining a fundamental understanding of brain anatomy and physiology. Proper analysis of calcium imaging data requires denoising, that is separating the signal from complex physiological noise. To analyze two-photon brain imaging data, we present a signal plus colored noise model in which the signal is represented as harmonic regression and the correlated noise is represented as an order autoregressive process. We provide an efficient cyclic descent algorithm to compute approximate maximum likelihood parameter estimates by combing a weighted least-squares procedure with the Burg algorithm. We use Akaike information criterion to guide selection of the harmonic regression and the autoregressive model orders. Our flexible yet parsimonious modeling approach reliably separates stimulus-evoked fluorescence response from background activity and noise, assesses goodness of fit, and estimates confidence intervals and signal-to-noise ratio. This refined separation leads to appreciably enhanced image contrast for individual cells including clear delineation of subcellular details and network activity. The application of our approach to in vivo imaging data recorded in the ferret primary visual cortex demonstrates that our method yields substantially denoised signal estimates. We also provide a general Volterra series framework for deriving this and other signal plus correlated noise models for imaging. This approach to analyzing two-photon calcium imaging data may be readily adapted to other computational biology problems which apply correlated noise models.National Institutes of Health (U.S.) (DP1 OD003646-01)National Institutes of Health (U.S.) (R01EB006385-01)National Institutes of Health (U.S.) (EY07023)National Institutes of Health (U.S.) (EY017098

Imaging of Functional Connectivity in the Mouse Brain

Functional neuroimaging (e.g., with fMRI) has been difficult to perform in mice, making it challenging to translate between human fMRI studies and molecular and genetic mechanisms. A method to easily perform large-scale functional neuroimaging in mice would enable the discovery of functional correlates of genetic manipulations and bridge with mouse models of disease. To satisfy this need, we combined resting-state functional connectivity mapping with optical intrinsic signal imaging (fcOIS). We demonstrate functional connectivity in mice through highly detailed fcOIS mapping of resting-state networks across most of the cerebral cortex. Synthesis of multiple network connectivity patterns through iterative parcellation and clustering provides a comprehensive map of the functional neuroarchitecture and demonstrates identification of the major functional regions of the mouse cerebral cortex. The method relies on simple and relatively inexpensive camera-based equipment, does not require exogenous contrast agents and involves only reflection of the scalp (the skull remains intact) making it minimally invasive. In principle, fcOIS allows new paradigms linking human neuroscience with the power of molecular/genetic manipulations in mouse models

Angular dependence of metamagnetic transitions in HoNi2B2C

Detailed measurements of M(2 K, H, theta) of HoNi2B2C, where theta is the angle that the applied field H makes with the [110] axis while remaining perpendicular to the crystallographic c axis, reveal three metamagnetic transitions with angular dependences H-c1 = (4.1 +/- 0.1 kG)/cos(theta), H-c2 = 8.4 +/- 0.2 kG/cos(phi), and H-c3 = (6.6 +/- 0.2 kG)/sin(phi), where phi = theta-45 is the angle from the [100] axis. The high-field saturated moment, M(sat) approximate to 10 mu(B)cos theta is consistent with the local moments being confined to the [110] direction. The locally saturated moments for fields between H-ci (i = 1, 2, 3) also manifest angular dependences that are consistent with combinations of local moments along [110] axes. Analysis of these data lead us to infer that the net distribution of moments is (up arrow down arrow up arrow down arrow up arrow down arrow) for H ) for H-c2 H-c3.This article is published as Canfield, P. C., S. L. Bud'ko, B. K. Cho, A. Lacerda, D. Farrell, E. Johnston-Halperin, V. A. Kalatsky, and Valery L. Pokrovsky. "Angular dependence of metamagnetic transitions in HoNi 2 B 2 C." Physical Review B 55, no. 2 (1997): 970. DOI: 10.1103/PhysRevB.55.970. Copyright 1997 American Physical Society. Posted with permission