How inert, perturbing, or interacting are cryogenic matrices? A combined spectroscopic (infrared, electronic, and x-ray absorption) and DFT investigation of matrix-isolated Iron, Cobalt, Nickel, and Zinc Dibromides

The interactions of FeBr2, CoBr2, NiBr2 and ZnBr2 with Ne, Ar, Kr, Xe, CH4 and N2 matrices have been investigated using IR, electronic absorption and X-ray absorption spectroscopies, as well as DFT calculations. ZnBr2 is linear in all the matrices. NiBr2 is linear in all but N2 matrices where it is severely bent. For FeBr2 and CoBr2 there is a more gradual change, with evidence of non-linearity in Xe and CH4 matrices as well as N2. In the N2 matrices the presence of νNN modes blue shifted from the “free” N2 values indicates the presence of physisorbed species, and the magnitude of the blue-shift correlates with the shift in the ν3 mode of the metal dibromide. In the case of NiCl2 and NiBr2 chemisorbed species are formed after photolysis, but only if deposition takes place below 10 K. There was no evidence for chemisorbed species for NiF2 and FeBr2 and in the case of CoBr2 the evidence was not strong

Action Without Awareness: Reaching to an Object You Do Not Remember Seeing

BACKGROUND: Previous work by our group has shown that the scaling of reach trajectories to target size is independent of obligatory awareness of that target property and that "action without awareness" can persist for up to 2000 ms of visual delay. In the present investigation we sought to determine if the ability to scale reaching trajectories to target size following a delay is related to the pre-computing of movement parameters during initial stimulus presentation or the maintenance of a sensory (i.e., visual) representation for on-demand response parameterization. METHODOLOGY/PRINCIPAL FINDINGS: Participants completed immediate or delayed (i.e., 2000 ms) perceptual reports and reaching responses to different sized targets under non-masked and masked target conditions. For the reaching task, the limb associated with a trial (i.e., left or right) was not specified until the time of response cuing: a manipulation that prevented participants from pre-computing the effector-related parameters of their response. In terms of the immediate and delayed perceptual tasks, target size was accurately reported during non-masked trials; however, for masked trials only a chance level of accuracy was observed. For the immediate and delayed reaching tasks, movement time as well as other temporal kinematic measures (e.g., times to peak acceleration, velocity and deceleration) increased in relation to decreasing target size across non-masked and masked trials. CONCLUSIONS/SIGNIFICANCE: Our results demonstrate that speed-accuracy relations were observed regardless of whether participants were aware (i.e., non-masked trials) or unaware (i.e., masked trials) of target size. Moreover, the equivalent scaling of immediate and delayed reaches during masked trials indicates that a persistent sensory-based representation supports the unconscious and metrical scaling of memory-guided reaching

Is Mislocalization during saccades related to the position of the saccade target within the image or to the gaze position at the end of the saccade?

A stimulus that is flashed around the time of a saccade tends to be mislocalized in the direction of the saccade target. Our question is whether the mislocalization is related to the position of the saccade target within the image or to the gaze position at the end of the saccade. We separated the two with a visual illusion that influences the perceived distance to the target of the saccade and thus saccade endpoint without affecting the perceived position of the saccade target within the image. We asked participants to make horizontal saccades from the left to the right end of the shaft of a Müller-Lyer figure. Around the time of the saccade, we flashed a bar at one of five possible positions and asked participants to indicate its location by touching the screen. As expected, participants made shorter saccades along the fins-in (<->) configuration than along the fins-out (>-<) configuration of the figure. The illusion also influenced the mislocalization pattern during saccades, with flashes presented with the fins-out configuration being perceived beyond flashes presented with the fins-in configuration. The difference between the patterns of mislocalization for bars flashed during the saccade for the two configurations corresponded quantitatively with a prediction based on compression towards the saccade endpoint considering the magnitude of the effect of the illusion on saccade amplitude. We conclude that mislocalization is related to the eye position at the end of the saccade, rather than to the position of the saccade target within the image

Why are saccades influenced by the Brentano illusion?

In the Brentano version of the Müller-Lyer illusion one part looks longer and the other looks shorter than it really is. We asked participants to make saccadic eye movements along these parts of the figure and between positions on the figure and a position outside the illusion. By showing that saccades from outside the figure are not influenced by the illusion, we demonstrate that the reason that saccades along the figure are influenced is that the incorrectly judged length is used to plan the amplitude of the saccade. This finding contradicts several current views on the use of visual information for action. We conclude that actions are influenced by visual illusions, but that such influences are only apparent if the action is guided by the attribute that is fooled by the illusion. © 2006 Springer-Verlag

The relative timing between eye and hand rapid sequential pointing is affected by time pressure, but not by advance knowledge

The present study examined the effect of timing constraints and advance knowledge on eye-hand coordination strategy in a sequential pointing task. Participants were required to point at two successively appearing targets on a screen while the inter-stimulus interval (ISI) and the trial order were manipulated, such that timing constraints were high (ISI = 300 ms) or low (ISI = 450 ms) and advance knowledge of the target location was present (fixed order) or absent (random order). Analysis of eye and finger onset and completion times per segment of the sequence indicated that oculo-manual behaviour was in general characterized by eye movements preceding the finger, as well as 'gaze anchoring' (i.e. eye fixation of the first target until completion of the finger movement towards that target). Advance knowledge of future target locations lead to shorter latency times of eye and hand, and smaller eye-hand lead times, which in combination resulted in shorter total movement times. There was, however, no effect of advance knowledge on the duration of gaze anchoring. In contrast, gaze anchoring did change as a function of the interval between successive stimuli and was shorter with a 300 ms ISI versus 450 ms ISI. Further correlation analysis provided some indication that shorter residual latency is associated with shorter pointing duration, without affecting accuracy. These results are consistent with a neural mechanism governing the coupling of eye and arm movements, which has been suggested to reside in the superior colliculus. The temporal coordination resulting from this coupling is a function of the time pressure on the visuo-manual system resulting from the appearance of external stimuli

Synthesis and properties of thallium(III) periodate

The reaction of [T1(H2O)(6)](3 +) with H5IO6 in aqueous acid solution over a range Tl-5(IO6)(3), which has been characterised by analysis, IR and UV-Vis spectroscopy The compound is amorphous, but I K- and Tl L-III edge EXAFS studies identify IO6 and TlO6 as the structural units present and a possible structure is proposed. The Tl(III)-IO6 system is compared with literature data on gallium and indium periodate complexes. The Tl(III)-IO6 system is compared with literature data on gallium and indium periodate complexes