1,998 research outputs found

    On-line control of grasping actions: object-specific motor facilitation requires sustained visual input

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    Dorsal stream visual processing is generally considered to underlie visually driven action, but when subjects grasp an object from memory, as visual information is not available, ventral stream characteristics emerge. In this study we use paired-pulse transcranial magnetic stimulation (TMS) to investigate the importance of the current visual input during visuomotor grasp. Previously, the amplitude of the paired-pulse motor evoked potentials (MEPs) in hand muscles before movement onset have been shown to predict the subsequent pattern of muscle activity during grasp. Specific facilitation of paired-pulse MEPs may reflect premotor–motor (PMC–M1) cortex connectivity. Here we investigate the paired-pulse MEPs evoked under memory-cued and visually driven conditions before grasping one of two possible target objects (a handle or a disc). All trials began with a delay period of 1200 ms. Then, a TMS pulse served as the cue to reach, grasp and hold the target object for 0.5 s. Total trial length was 5 s. Both objects were continually visible in both conditions, but the way in which the target object was designated differed between conditions. In the memory-cued condition, the target object was illuminated for the first 200 ms of the trial only. In the visually driven condition, the target object was illuminated throughout the 5 s trial. Thus, the conditions differed in whether or not the object to be grasped was designated at the time of movement initiation. We found that the pattern of paired-pulse MEP facilitation matched the pattern of object-specific muscle activity only for the visually driven condition. The results suggest that PMC–M1 connectivity contributes to action selection only when immediate sensory information specifies which action to make

    The Millennium Galaxy Catalogue: Star counts and the Structure of the Galactic Stellar Halo

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    We derive a star catalogue generated from the images taken as part of the 37.5 sq. deg Millennium Galaxy Catalogue. These data, alone and together with colours gained from the Sloan Digital Sky Survey Early Data Release, allow the analysis of faint star counts (B(MGC) < 20) at high Galactic latitude (41 < b < 63), as a function of Galactic longitude (239 < l < 353). We focus here on the inner stellar halo, providing robust limits on the amplitude of substructure and on the large-scale flattening. In line with previous results, the thick disk, an old, intermediate-metallicity population, is clearly seen in the colour-magnitude diagram. We find that the Galactic stellar halo within ~10 kpc (the bulk of the stellar mass) is significantly flattened, with an axial ratio of (c/a) =0.56 +/- 0.01, again consistent with previous results. Our analysis using counts-in-cells, angular correlation functions and the Lee 2D statistic, confirms tidal debris from the Sagittarius dwarf but finds little evidence for other substructure in the inner halo, at heliocentric distances of < 5 kpc. This new quantification of the smoothness in coordinate space limits the contribution of recent accretion/disruption to the build-up of the bulk of the stellar halo.Comment: Accepted for publication in MNRAS (figs 16 and 17 degraded here

    Identification of hepatitis a virus mimotopes by phage display, antigenicity and immunogenicity

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    A phage-displayed peptide approach was used to identify ligands mimicking antigenic determinants of hepatitis A virus (HAV) for the first time. Bacteriophages displaying HAV mimotopes were isolated from a phage-display peptide library by affinity selection on serum antibodies from hepatitis A patients. Selected phage-peptides were screened for reactivity with sera from HAV infected patients and healthy controls. Four cloned peptides with different sequences were identified as mimotopes of HAV; three of them showed similarity in their amino acid sequences with at least one of the VP3 and VP1 antigenic proteins of HAV. One clone was recognised by 92% of the positive sera. The phagotopes competed effectively with HAV for absorption of anti-HAV-specific antibodies in human sera, as determined by ELISA. The four phage clones induced neutralising anti-HAV antibodies in immunised mice. These results demonstrate the potential of this method to elucidate the disease related epitopes of HAV and to use these mimotopes in diagnostic applications or in the development of a mimotope-based hepatitis A vaccine without the necessity of manipulation of the virus

    Production of Virginia Peanuts in the Rolling Plains and Southern High Plains of Texas

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    4 pp., 1 mapCultural practices such as crop rotation, maintaining plant nutrition, irrigation management and disease management are crucial for the successful production of Virginia peanuts. This publications describes these and other production considerations

    My Ain Folk

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    Tan cover with bold wordshttps://scholarsjunction.msstate.edu/cht-sheet-music/6301/thumbnail.jp

    Ventral Premotor-Motor Cortex Interactions in the Macaque Monkey during Grasp: Response of Single Neurons to Intracortical Microstimulation

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    Recent stimulation studies in monkeys and humans have shown strong interactions between ventral premotor cortex (area F5) and the hand area of primary motor cortex (M1). These short-latency interactions usually involve facilitation from F5 of M1 outputs to hand muscles, although suppression has also been reported. This study, performed in three awake macaque monkeys, sought evidence that these interactions could be mediated by short-latency excitatory and inhibitory responses of single M1 neurons active during grasping tasks. We recorded responses of these M1 neurons to single low-threshold (<= 40 mu A) intracortical microstimuli delivered to F5 sites at which grasp-related neurons were recorded. In 29 sessions, we tested 232 M1 neurons with stimuli delivered to between one and four sites in F5. Of the 415 responses recorded, 142 (34%) showed significant effects. The most common type of response was pure excitation (53% of responses), with short latency (1.8-3.0 ms) and brief duration (similar to 1 ms); purely inhibitory responses had slightly longer latencies (2-5 ms) and were of small amplitude and longer duration (5-7 ms). They accounted for 13% of responses, whereas mixed excitation then inhibition was seen in 34%. Remarkably, a rather similar set of findings applied to 280 responses of 138 F5 neurons to M1 stimulation; 109 (34%) responses showed significant effects. Thus, with low-intensity stimuli, the dominant interaction between these two cortical areas is one of short-latency, brief excitation, most likely mediated by reciprocal F5-M1 connections. Some neurons were tested with stimuli at both 20 and 40 mu A; inhibition tended to dominate at the higher intensity
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