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Concentrations of total arsenic and of arsenic species were determined by ICPMS and HPLC-ICPMS in terrestrial plant samples. The arsenic concentration in plant samples from the contaminated sites ranged from 1.14 to 98.5 mg kg(-1) (dry mass). However, a very high value, exceeding largely this range was found in a moss sample growing in the contaminated area (1750 mg kg(-1)). Plants growing in a non-contaminated area with similar geological characteristics contained 0.06-0.58 mg As kg(-1). Plant samples from different species were selected and extracted with water, water/methanol (9+1, v/v), and water/methanol (1+1, v/v). Water/methanol (9+1, v/v) was selected as extractant for the speciation analysis for all the plant samples. The extraction efficiencies ranged from 3.0% to 41.4%, with good agreement between samples from the same plant species. Arsenite and/or arsenate were found in all the plant samples. Additionally, methylarsonate (MA), dimethylarsinate (DMA), trimethylarsine oxide (TMAO) and tetramethylarsonium ion (TETRA) were also identified in several plants, and in some cases MA and DMA were the main species found. TMAO, which is usually found as a trace constituent in organisms, was also a significant arsenical in one of the studied samples, where it constituted 24% of the extracted arsenic. In the present study, the patterns of arsenic species varied with the plant species and much higher proportion of organoarsenicals was found in plants from the more contaminated sites.

The influence of soil contamination by inorganic and organic arsenic compounds on uptake, accumulation, and transformation of arsenic in pepper (Capsicum annum L.) was investigated in greenhouse pot experiments under controlled conditions. Pepper plants were cultivated in substrate amended by aqueous solutions of arsenite, arsenate, methylarsonic acid (MA), and dimethylarsinic acid (DMA) applied individually into cultivation substrate at concentrations of 15 mg As per kg of substrate. The plant availability of the arsenicals increased in the order arsenite = arsenate < MA < DMA. The highest arsenic concentrations were found in roots followed by stems, leaves, and fruits regardless of arsenic compound applied. In the control samples of pepper fruits, As(III), As(V), and DMA were present (25%, 37%, and 39% of the water-extractable arsenic). In control stems + leaves and roots, As(V) was the major compound (63% and 53% in a phosphate buffer extract) followed by As(III) representing 33% and 42%. Additionally, low concentrations (not exceeding 5%) of DMA and MA were detected as well. In all the soils analyzed after the first harvest of pepper fruits, arsenate was the dominating compound followed by arsenite. Methylarsonic acid, methylarsonous acid, and DMA were present at varying concentrations depending on the individual soil treatments. In the treated plants, the arsenic compounds in plant tissues reflected predominantly the extractable portions of arsenic compounds present in soil after amendment, and this pattern was more significant in the first part of vegetation period. The results confirmed the ability of generative parts of plants to accumulate preferably organic arsenic compounds, whereas in the roots and aboveground biomass, mainly inorganic arsenic species are present. Evidently, the source of soil arsenic contamination affects significantly the extractable portions of arsenic compounds in soil and subsequently the distribution of arsenic compounds within the plants.

We report results from the first investigation of the human metabolism of arsenic-containing lipids (arsenolipids), significant arsenic constituents of some seafood products. Two male volunteers ingested canned cod liver and the arsenic metabolites in their urine were monitored by high-performance liquid chromatography inductively coupled plasma mass spectrometry over a 66-h period. Volunteer A consumed 85 g (wet mass) of cod liver containing a total of approximately 120 microg arsenic, 77% of which was present as arsenolipids, and volunteer B consumed 85 g (wet mass) of cod liver, 25% of which was present as arsenolipids, together with 20 g of cod liver oil, containing a total of about 180 microg arsenic. The structures of the arsenolipids are currently unknown, whereas the majority of the non-lipid arsenic in the cod liver was identified as arsenobetaine, which was excreted unchanged. The arsenolipids were rapidly metabolised to water-soluble compounds and excreted in the urine; peak arsenic concentrations were recorded between 7 and 15 h (volunteer A) and between 6.5 and 15 h (volunteer B), and by the end of the experiment about 90% of the ingested arsenic had been accounted for in the urine for both volunteers. The major arsenolipid metabolite was dimethylarsinate (DMA), constituting 73% (volunteer A) or 41% (volunteer B) of the total urinary arsenic, and most of the remaining arsenolipid-derived arsenic, constituting about 10% (volunteer A) and 5% (volunteer B), comprised four novel arsenic-containing fatty acids, namely oxo-dimethylarsenopropanoic acid, thio-dimethylarsenopropanoic acid, oxo-dimethylarsenobutanoic acid, and thio-dimethylarsenobutanoic acid. Unchanged arsenobetaine (15% for volunteer A and 51% for volunteer B) made up the remaining urinary arsenic together with trace quantities of other, mostly unknown, arsenicals. In a second experiment (volunteer A only), performed with pure cod liver oil, which contains only arsenolipids, DMA and the same four arsenic fatty acids were excreted in the urine. The study shows that arsenolipids in cod liver are bioavailable, and that they are quickly biotransformed to several water-soluble arsenicals, the structures of which suggest that the native arsenolipids contain a dimethylarsine oxide moiety.

In contrast to the large body of data on naturally-occurring arsenic compounds in marine organisms, relatively little is known about arsenic speciation in freshwater biota. We report an investigation using HPLC-ICPMS into the arsenic compounds in five species of freshwater mussels collected from five sites from the Danube in Hungary. Total arsenic concentrations in the mussels ranged from 3.8-12.8 mg As kg(-1). The arsenic speciation patterns were broadly similar for mussels representing each of the five species and five sites, but quite different from those reported for marine mussels. The major extractable arsenicals were two oxo arsenosugars (glycerol sugar and phosphate sugar), and their thio analogues (thio glycerol sugar and thio phosphate sugar). Arsenobetaine, usually the major arsenical in marine organisms, was not a significant compound in the freshwater mussels and was detected in only three of the 11 samples. This is the first report of thio arsenosugars in freshwater biota and suggests that these compounds may be common and widespread naturally-occurring arsenicals.

Lipid-soluble arsenicals (arsenolipids) occur in a wide range of biological samples where they may play a key role in the biosynthesis of organoarsenic compounds from inorganic arsenic. The study of these compounds has been hindered, however, by the lack of a suitable analytical technique able to separate and measure the various lipid species. As a source of arsenolipids, we used 10 crude fish oils from various regions of the world. Total arsenic analyses on the fish oils, performed with ICPMS following acid digestion with microwave-assisted heating, gave concentrations from 4.3 to 10.5 mg As kg(-1). All of the arsenic was soluble in non-polar solvents such as hexane. Analysis of the fish oils for arsenolipids was performed by normal phase HPLC-ICPMS with various mixtures of organic solvents as mobile phases. Inherent problems of instability associated with the introduction of organic solvents to the plasma were overcome by the use of reduced column flow, a chilled spray chamber, and the addition of oxygen directly to the plasma. All ten fish oils appeared to contain the same 4-6 major arsenolipids, but in varying amounts depending on the origin of the fish. Further chromatography with both normal phase and reversed-phase conditions on some of the oils indicated the presence of many more minor arsenolipids. Quantification was achieved by external calibration against triphenylarsine oxide or triphenylarsine sulfide, and the sum of species following HPLC of the oils matched well the total arsenic results (92-107%). The method was applied to samples of food supplements (fish oil capsules) and a packaged food product (cod liver) whereby arsenolipids were measured and found to be significant arsenic constituents. This study represents the first attempt to directly measure intact arsenolipids and, with appropriate sample preparation, may be suitable for quantitative measurement of these arsenicals in a range of biological samples, including foodstuffs.

Two novel thio arsenosugars have been identified by liquid chromatography-mass spectrometry as significant arsenic constituents in samples of mussels.

It is generally accepted that the use of the hydride generation method to produce volatile analytes from arsenic compounds is restricted to the two inorganic forms (As(III) and As(V)) and the three simple methylated species methylarsonate (MA), dimethylarsinate (DMA), and trimethylarsine oxide. We report here that arsenosugars, major arsenic compounds in marine organisms, produce volatile analytes by the hydride generation (HG) method without a prior mineralization/oxidation step and that they can be quantitatively determined using HPLC-HG-ICPMS. The hydride generation efficiency depends on the type of hydride generation system and is influenced by the concentration of HCl and NaBH(4). For the four arsenosugars investigated, the hydride generation efficiencies were approximately 21-28% (or 4-6%, depending on the HG system) that obtained for As(III) under conditions optimized for As(III). This hydride efficiency was less than that shown by MA ( approximately 68% relative to As(III)) and DMA ( approximately 75%) but greater than that displayed by As(V) ( approximately 18%). Analysis of two species of brown algae, Fucus serratus and Hizikia fusiforme, by HPLC-HG-ICPMS produced results comparable with those obtained from other techniques used in our laboratory (HPLC-ICPMS and LC-ESMS for F. serratus) and with results from other laboratories taking part in a round robin exercise (H. fusiforme). This study shows for the first time the quantitative determination of arsenosugars using the hydride generation method without a decomposition step and has considerable implications for analytical methods for determining inorganic arsenic based on the formation of volatile hydrides.

We performed focal electroretinography (FERG) in 10 patients with reduced vision of unknown cause. No patient gave a family history of uncorrectably reduced vision, and none had taken any drug known to damage the retina. Visual acuity claims ranged from 20/40 to finger counting. Color discrimination was reduced in all but one patient. Visual field sensitivity was reduced nonspecifically in five of the six patients who could perform perimetry reliably. Ophthalmoscopy showed no pertinent abnormality in four of 10 patients, mildly reduced foveal reflex in two of 10, arteriolar narrowing in two of 10, foveal pigment disturbance in one of 10, and preretinal gliosis in one of 10. Flash visual evoked potential (VEP) testing showed no abnormality in seven of 7 patients. The pattern VEP was reduced or delayed in five of 5 patients, only one of whom showed the expected amplitude loss with decreasing check size. Five patients completed full-field electroretinography, six patients completed fluorescein angiography, and none showed pertinent abnormality on either test. FERG was performed in both eyes of seven patients and in one eye of three others. Signals were non-recordable from four eyes, abnormal in nine, equivocal in three, and normal in one. The severity of FERG abnormality did not correlate with the severity of acuity loss. FERG abnormalities were found in fourteen of 17 eyes of 10 patients with vision loss out of proportion to clinical findings. In these patients only one of 5 pattern VEP tests, none of 5 full-field ERGs, and none of 7 fluorescein angiograms suggested correspondingly severe maculopathy. The FERG results in these cases mitigated suspicions of nonorganic vision loss and permitted speedier referral to retinal disease and low vision specialists.

Background: Laser pointers have been used inappropriately to harass and "dazzle" victims. Reports of retinal damage caused by pointers have also been circulated in the popular press., Methods: Information on pointer abuse was collected from the literature and through discussions with specialists., Results: Few, if any, documented cases of permanent retinal damage caused by laser pointers could be found. For actual damage to occur, viewing, times need to exceed approximately 10 seconds. Exposures of this duration would require the person being lased to cooperate by holding fixation on the laser beam., Conclusions: Although the risk of permanent retinal damage from a laser-pointer beam is minimal, other risks include dazzle, annoyance, and concern that a weapon-aiming device rather than a pointer is generating the laser beam.

Purpose: Changes in refractive error have been reported after strabismus surgery. The influence of extraocular muscle tension on corneal topography is thought to be an important mechanism contributing to this alteration. This study investigates topographic changes after strabismus surgery in human beings., Methods: The corneal topography of 63 eyes of 43 patients who underwent either strabismus or optic nerve sheath fenestration (ONSF) surgery was measured before and after operation. The ONSF surgery involved removing and reattaching the medial rectus muscle, thus acting as a control for the strabismus procedures. Corneal power was measured centrally and at 1.5 and 3.0 mm in 8 meridians. Analysis of variance was performed to compare the difference in preoperative and post-operative corneal power for all procedures and comparing recessions, resections, combined recession and resection, and ONSF as grouped procedures., Results: All groups showed a significant change in preoperative to postoperative corneal power (P< .01). A significant change was seen between all grouped procedures except when the resection was compared with ONSF and compared with recession., Conclusions: Change in the tension of 1 muscle does not produce a change in the adjacent quadrant as much as it produces a significant change in the entire corneal surface, which illustrates the interaction and interdependence all corneal positions have with respect to each other.

Objectives: To examine the clearance of cyclosporine after intravitreal injection and to assess the kinetics and toxic effects of an intravitreal device that provides sustained delivery of cyclosporine., Methods: Rabbits were divided into two groups to evaluate (1) the elimination kinetics after 1-microgram and 10-microgram intravitreal injections of cyclosporine and (2) the levels produced after implantation of a device that contained cyclosporine over 6 months. The toxic effects of the intravitreal device over 6 months were assessed in rabbits and cynomolgus monkeys., Results: After the 10-microgram injection, the half-life was longer (10.8 hours vs. 4.2 hours) and the distribution volume was smaller (1.7 mL vs 3.2 mL) than after the 1-microgram injection. This difference can be attributed to saturable partitioning of the drug. The device resulted in a vitreous concentration of approximately 500 ng/mL throughout the study period. In the rabbit it resulted in reversible lens opacification and decreased b-wave amplitude. This toxic effect was not detected in the monkey., Conclusions: The device produces sustained intravitreal levels of cyclosporine. Although it was associated with reversible toxic effects in the rabbit, it was well tolerated in primates. Sustained-release implants are a promising new treatment for chronic uveitis.

Direct evidence of a distinct cortical binocular pathway has been provided by the production of nonlinear (difference) beats from dichoptic luminance stimulation in stereonormal adults and the absence or diminution of these beats in stereoblind subjects. We have investigated a clinically useful application of this technique in a pediatric population with potentially abnormal binocular vision. We recorded dichoptic luminance beat visual evoked potentials (VEPs) from 20 children (ages 7 months to 8 years) with abnormal binocular ability secondary to strabismus and/or amblyopia and compared this to a control group of 20 children with normal binocularity. Stereoblind children generated significantly lower dichoptic signal-to-noise ratios than stereonormal children (P < .001). Responses to monoptic multifrequency flicker were not significantly different between the two groups (P = .936). This dichoptic VEP can be performed quickly and easily on young children and gives a quantitative assessment of cortical binocularity that may not be determinable by standard clinical methods. This technique may also prove useful for the preoperative gradation of binocular potential and prediction of postoperative binocular fusion.

Electrophysiological models of visual evoked potential recording have assumed that response variability is caused predominantly by random noise added to a true steady signal. Since neuronal geometry has a fractal structure, neural activity may demonstrate deterministic nonlinear dynamics, i.e., chaos. We recorded several-minute time-series traces of the visual evoked potential magnitude in response to full-field flicker from three glaucoma patients and one normal subject. When plotted in phase space, the steady-state response derived from a lock-in amplifier shows an apparent so-called strange attractor (extended nonrepeating loops) rather than the pattern expected from a signal-plus-noise model (a fuzzy dot). The fractal dimension of this attractor may be a more sensitive indicator of early optic-nerve damage than are visual evoked potential latency or amplitude measures.

Q-switched neodymium-YAG (infrared) laser lesions at energies up to and including retinal hemorrhages were placed under visual control in the parafovea and the fovea of anesthetized monkeys. Visual-evoked potential (VEP) data were obtained by parallel analog (vector voltmeter) techniques from scalp electrodes in response to high luminance counterphasing sine wave gratings. The gratings were swept downward in spatial frequency to determine an acuity estimate by recording of the VEP magnitude increase onset. Acuity estimates were determined immediately post-exposure and at 15 sec intervals up to 12 min. These were analyzed as a function of laser exposure site and retinal lesion produced. Significant delays in VEP lock-in were demonstrated in subjects that had parafoveal burns or parafoveal subretinal hemorrhages. Foveal burns caused severe short-term fluctuations before a sustained decrease in acuity. Contained foveal hemorrhages produced sustained acuity losses. Foveal exposures that did not produce an immediately visible lesion did not produce measurable changes in VEP response lock-in time. These results probably are independent of visible flash effects and indicate that there may be a transient neural shock effect from parafoveal lesions that can affect the fovea.

To evaluate the efficacy of multifocal contact lenses in the correction of presbyopic symptoms we fit six young monocular aphakic patients with four different bifocal contact lenses (ACC, Tangent Streak, VFL, and Constavu). Each patient had 20/20 uncorrected vision and normal accommodation in the other eye. We evaluated both subjective and objective parameters of comfort and vision for all four lenses. We found no significant overall performance advantage among the four lenses based on comfort, visual satisfaction, visual acuity, contrast sensitivity, or wear-related corneal complications.

Current treatment of cytomegalovirus retinitis in patients with acquired immunodeficiency syndrome involves frequent intravenous administration of sodium ganciclovir that often results in unacceptable side effects. We have developed devices that release ganciclovir at rates of 2 micrograms/h and 5 micrograms/h in vitro. When implanted into the vitreous of rabbit eyes, mean intravitreal ganciclovir levels of 9 mg/L and 16 mg/L were maintained for more than 80 and 42 days, respectively. Devices were well tolerated, with no toxic effects attributable to the polymers used in the devices. This investigation indicates that these devices can maintain therapeutic levels of drug for extended periods and are well tolerated in the rabbit eye. They may prove useful in the clinical management of cytomegalovirus retinitis in patients with acquired immunodeficiency syndrome.

Over a one-year period we evaluated subjective and objective factors associated with extended wear of Boston IV rigid gas permeable contact lenses. Patients wore the lens on an extended wear schedule, with removal at 2-week intervals for cleaning. We performed keratometry and endothelial cell counts and measured visual acuity, contrast sensitivity, refraction, and corneal thickness at the initial visit (with patients wearing their former glasses or soft or hard lenses) and again at 6 and 12 months (with patients wearing the Boston IV lens). Twenty-four of 31 patients (77%) completed the study. All measured parameters were checked for statistically significant change over time. Contrast sensitivity increased at all spatial frequencies tested, with the largest increments occurring at higher frequencies (P less than .001). The other parameters showed no significant changes (P greater than .05). Our data support the use of contrast sensitivity for qualitative assessment of visual function among contact lens wearers and suggest that contrast sensitivity testing may prove to be a more effective means of evaluating visual acuity in contact lens wearers over time than Snellen acuity.

Argon laser pretreatment prior to Nd:YAG laser iridotomy may decrease the incidence of operative hemorrhage. In a prospective, randomized clinical trial involving 12 patients (24 eyes), one eye was randomly assigned treatment with the Nd:YAG laser alone, while the other eye was pretreated with argon laser photocoagulation immediately prior to Nd:YAG laser. Eight of the 12 eyes (67%) treated with Nd:YAG laser alone had operative hemorrhages; only 2 of the 12 (17%) pretreated eyes did. Thus, argon laser pretreatment significantly reduced the incidence of hemorrhage during Nd:YAG iridotomy (P = .012).

The ERG can be helpful to the neurologist who must evaluate patients with known or suspected retinal disease. The test is most useful in detecting (or excluding) outer retinal disease, especially in presymptomatic, very young, or mentally enfeebled patients. It can also help in interpreting the meaning of an abnormal VEP.

A series of experiments was performed to determine the parameters necessary to produce immediate measurable changes in the visual system of nonhuman primates after exposure of the fovea to laser radiation. The parameters investigated were stimulus spatial frequency (1.6 and 2.8 c/deg), size of the visual field stimulated (30 and 3.6 degrees), retinal diameter of the laser exposure (50 and 500 micron), and total intraocular energy. Steady-state visual evoked potentials (VEP's) were recorded from cynomolgus monkeys in response to an oscillating grating. Single 20 ns Q-switched ruby laser pulses (694.3 nm) were directed into the fovea of the experimental eye during the pattern stimulation. No immediate effects on the VEP were noted. Strong delayed effects occurred 45 to 120 s postexposure and were characterized by large phase shifts in the response signal as referenced to the stimulus, magnitude decreases, variance increases, and a loss of waveform correlation with pre-exposure baseline signals. These effects persisted for approximately 30 s before the VEP again became normally re-entrained.

A program in BASIC for calculation of intraocular lens power, derived from previously published formulas, is presented for use on small computer systems.

The effects of foveal exposure to near maximum permissible levels of broad-band light from lamps of differing flash durations and visual angle subtense on steady-state visual evoked potentials ( SSVEP 's) were measured in four human volunteers. SSVEP 's in response to a counterphasing checkerboard pattern were recorded with a two-phase vector voltmeter used as an analog fourier analyzer and were averaged across repeated presentation of the flash from each lamp. Two microsecond flashes of approximately 0.4 degrees have minimal, although significant effects on early visual processing of a 2.77 degrees diameter 6/24 (20/80) target. Five hundred microsecond flashes of equivalent size have greater effects; larger flashes (11.3, degrees 500 mus) produced afterimages that totally obscured the target for approximately 3.4 s and also reduced the SSVEP to near zero. Recovery of the SSVEP was subjectively correlated with afterimage duration rather than target obscuration . Therefore, single short small retinal image flashes may have minimal transient effects on photopic suprathreshold vision.

Anatomic evidence indicates that glaucoma initially destroys large axons before affecting smaller ones. Large axonal size has been correlated with fast, transiently responding retinal ganglion cells (alpha/Y cells). A second population of cells (X cells) does not follow flicker stimulation to as high a frequency as Y cells. The luminance flicker visual-evoked potential (VEP) shows two response maxima as a function of temporal frequency. These two response peaks may indicate driving of the flicker VEP by two separate neuronal populations, possibly X and Y cells. The authors have recorded flicker VEPs as a function of frequency from both normal subjects and glaucoma patients with asymmetric visual field loss in various stages of their disease. The data obtained demonstrate loss of high flicker rate responses apparently preceding and correlated with perimetric field loss and stage of glaucoma. Flicker VEP responses below 13 Hz tend to be preserved, whereas above this frequency the response attenuation is directly proportional to the severity of visual loss. This technique may provide an early warning of ganglion cell loss in the early stages of this disease.

Electroretinograms (ERG's) and visual evoked potentials (VEP's) were recorded from four cynomolgus monkeys in response to a sinusoidally flickering argon laser beam (514 nm) producing a 50-micron spot on the fovea. Super-position of a 20-Hz train of six pulses of Q-switched (120 ns) frequency-doubled neodymium laser light (532 nm) at "safe" exposure energies in 250 ms had no significant effects on the ERG (p greater than 0.05). The VEP was disrupted significantly (p less than 0.001) but demonstrated recovery within 500 ms of the initial pulse. Therefore, flash effects of pulsed visible lasers at these doses on suprathreshold luminance processing are probably limited only to the exposure period.

Steady-state visual evoked potentials (VEP's) were recorded from four cynomolgus monkeys in response to a sinusoidally oscillating 10 degrees helium-neon laser speckle field (632.8 nm), moving vertically 2.5 degrees at 8 shifts per second. A 5-pulse flash train at the maximum permissible exposure (MPE) dose from a collimated Q-switched frequency-doubled neodymium laser (532 nm) was superimposed on the foveal stimulus and the subsequent disruption and recovery of the VEP measured. Minimal disruption of the response signal magnitude was demonstrated (0.1 greater than p greater than 0.05) which recovered within 300 ms of the termination of the pulse train. A small but significant (p less than 0.01) disruption of phase entrainment was also noted that recovered within the same period. This is contrasted with a second experiment with three monkeys in which an argon (514 nm) laser served both as the speckle stimulus source and as the shuttered flash. Exposure to collimated MPE argon radiation for 250 ms immediately depressed the VEP (97%, p less than 0.01) and showed recovery to 70% of the pre-flash baseline only after 3 s. Phase lock was also severely degraded for several seconds. These results imply that visual processing of nonacuity-limited medium contrast stimuli with broad spatial frequency content will probably not be materially affected by ultra-short pulsed laser exposure at these energy levels and frequencies. However, even safe levels of collimated continuous laser light may have severe effects on vision that could parallel flash effects seen with Xenon discharge flash lamps.

Detecting a target in a visually noisy back-ground depends on the ability of the observer to discriminate the target from the surrounding terrain. Visible laser irradiation at less than damage levels may act as a masking source by reducing the observer's ability to resolve differences in the visual scene. The experiment reported here specifically investigates the comparability of shuttered CW and Q-switched visible lasers to alter/degrade color discrimination. Visual evoked potentials (VEP's) were used to examine the short time course effects in monkeys of luminance-matched flashes from a 694 nm ruby Q-switched laser and 100 ms shuttered krypton CW laser (676, 568, and 531 nm lines). The test stimulus was a shifting pattern of alternating luminance-matched 510 and 550 nm green bars. With flashes equated to 4.8 log T-s, similar flash effect curves were seen, demonstrating 1.5-s changes in response magnitude. This level of flash did not extinguish the response to the stimulus. The flash effects curve was "W"-shaped, with an intermediate signal peak occurring at approximately 500 ms after the flash and whose level exceeded the baseline magnitude. The hypothesized mechanism for this result is an induced luminance imbalance caused by a transient shift in the peak color responsiveness of the visual system, which recovers with two different time constants. It is concluded that red and green colored laser flashes shift the color balance transiently in the visual system (yellow flashes to a lesser extent); thus, targets may change both hue and brightness after an observer receives colored flashes.(ABSTRACT TRUNCATED AT 250 WORDS)

Steady-state visual evoked potentials (VEP's) were elicited from human volunteers by contrast reversal of a 43% contrast checkerboard pattern resolvable with 6/24 (20/80) Snellen acuity. Superimposed on the fixation point was a Xenon flash lamp subtending 0.358 degrees visual angle, which produced a 0.05 J/cm2 sr flash in 2 microseconds (full width, half maximum). Single pulses of light had no significant effect on the VEP. Increasingly significant decreases in VEP signal magnitude were noted with 2 and 5 pulses of 20 Hz white light. No disruption of VEP phase entrainment was noted with any of the flash exposures. Partial reciprocity was demonstrated between number of flashes at this frequency and response decrement.