Ultra fast symmetry and SIMD-based projection-backprojection (SSP) algorithm for 3-D PET image reconstruction.

Remarkable progress in positron emission tomography (PET) development has occurred in recent years, in hardware, software, and computer implementation of image reconstruction. Recent development in PET scanners such as the high-resolution research tomograph (HRRT) developed by CTI (now Siemens) represents such a case and is capable of greatly enhanced resolution as well as sensitivity. In these PET scanners, the amount of coincidence line data collected contains more than 4.5 x 10(9) coincidence lines of response generated by as many nuclear detectors as 120 000. This formidable amount of data and the reconstruction of this data set pose a real problem in HRRT and have also been of the major bottle neck in further developments of high resolution PET scanners as well as their applications. In these classes of PET scanners, therefore, obtaining one set of reconstructed images often requires many hours of image reconstruction. For example, in HRRT with full data collection in a normal brain scan (using SPAN 3), the image reconstruction time is close to 80 min, making it practically impossible to attempt any list-mode-based dynamic imaging since the image reconstruction time would take many days (as much as 43 h or more for 32-frame dynamic image reconstruction). To remedy this data-handling problem in image reconstruction, we developed a new algorithm based on the symmetry properties of the projection and backprojection processes, especially in the 3-D OSEM algorithm where multiples of projection and back-projection are required. In addition, the single-instruction multiple-data (SIMD) technique also allowed us to successfully incorporate the symmetry properties mentioned above, thereby effectively reducing the total image reconstruction time to a few minutes. We refer to this technique as the symmetry and SIMD-based projection-backprojection (SSP) technique or algorithm and the details of the technique will be discussed and an example of the application of the technique to the HRRT's OSEM algorithm will be presented as a demonstration.

A neuromodulatory role for oxytocin within the supramammillary nucleus.

Oxytocin functions as both a neurohypophysial hormone and central neuromodulatory peptide, and has been implicated in reproductive behaviours, anxiety and reward, as well as facilitation of the neuroendocrine milk-ejection reflex. A potential substrate for oxytocin is the supramammillary nucleus (SuM), a structure that contains oxytocin binding sites and serves as an important relay within the limbic system. Hence, this study investigated the neuromodulatory role of oxytocin within the SuM. Firstly, the effect of oxytocin on neuronal firing within the SuM was studied, using in vitro brain slices from virgin female rats. Oxytocin (10(-6)M) excited approximately 50% of SuM neurones, and similar results were obtained with the selective oxytocin agonist, Thr(4) Gly(7) oxytocin (TGOT) (10(-6) and 10(-7)M). The remaining neurones were unaffected. The TGOT response was blocked by application of the oxytocin antagonist, [d(CH(2))51,Tyr(Me)(2),Thr(4),Orn(8),Tyr-NH29]-vasotocin. Repeat doses of TGOT caused diminution of the response, indicative of desensitisation. In the second series of experiments, immunocytochemical techniques were used to study the oxytocinergic innervation of the SuM. The supramammillary decussation was found to contain numerous oxytocinergic fibres, and some could be seen coursing ventrally to enter the SuM. Whereas, some were clearly "en passant" fibres innervating the neurohypophysis, others followed a more convoluted and branching course, and appeared to terminate within the nucleus. Finally, in vivo microinfusion studies investigated whether oxytocin injected into the SuM facilitated the milk-ejection reflex, a well known action of central oxytocin. Oxytocin microinfusion in the region of the SuM caused a pronounced facilitation of the reflex, contrasting with the much smaller effects of microinfusions made rostral or caudal to the nucleus. Collectively, these results strongly support a neuromodulatory role for oxytocin within the SuM. This could have important implications for understanding the diverse neuroendocrine and behavioural functions of central oxytocin, including its role in reward.

Synergistic antinociception between zaprinast and morphine in the spinal cord of rats on the formalin test.

BACKGROUND AND OBJECTIVE: The cyclic guanosine monophosphate level, which causes an antinociception, is increased in cells as a direct result of phosphodiesterase inhibition. This study used a nociceptive test to examine the nature of the pharmacological interaction between intrathecal zaprinast, a phosphodiesterase inhibitor, and morphine. METHODS: Catheters were inserted into the intrathecal space through an incision in the atlantooccipital membrane of male Sprague-Dawley rats. As a nociceptive model, 50 microL of a 5% formalin solution was injected into the hind paw. After observing the effect of zaprinast (37, 111, 369 nmol) and morphine (1, 4, 10, 40 nmol) alone, the interactions of their combination were examined by an isobolographic analysis. RESULTS: Intrathecal zaprinast (P < 0.05) and morphine (P < 0.05) dose-dependently suppressed the flinching observed during phase 1 and phase 2 in the formalin test. The ED50 values (95% confidence intervals) of zaprinast and morphine in phase 1 were 161.9 (87.9-298.3) and 11.6 nmol (4.8-27.9 nmol), respectively. The phase 2 ED50 values (95% confidence intervals) of zaprinast and morphine were 229.9 (142.5-370.9) and 3.9 nmol (1.9-7.6 nmol), respectively. Isobolographic analysis revealed a synergistic interaction after intrathecal delivery a zaprinast-morphine mixture in both phases. The ED50 values of (95% confidence intervals) zaprinast in the combination of zaprinast with morphine in phase 1 and phase 2 were 14.2 (4.9-40.6) and 10.4 nmol (3-35.9 nmol), respectively. CONCLUSIONS: Intrathecal zaprinast and morphine are effective against acute pain and facilitated pain state. Zaprinast interacts synergistically with morphine.

Allergenicity test of genetically modified soybean in Sprague Dawley rats.

Allergenicity of genetically-modified (GM) soybean was evaluated in male Sprague Dawley rats. To confirm the GM soybean used in this study, the polymerase chain reaction (PCR) was performed using the chromosomal DNA of soybeans. The PCR result provided the clear discrimination of genetically-modified (GM) soybeans. To evaluate the allergenicity of GM soybean and non-GM control one, the soybean homogenate was sensitized subcutaneously 3 times a week for 3 weeks. The doses of soybean were 0, 2 and 20 mg/kg in the protein basis. A week after the last sensitization, antisera were recovered from individual animals. When the sera were injected intradermally on the clipped back of unsensitized rats with various dilutions, followed by a challenge with 20 mg/kg of soybean homogenate containing 1% Evans blue, no sign of passive cutaneous anaphylaxis reaction was detected. In addition, when the sera were treated in the cultures of peritoneal mast cells, the increase of histamine release by anti-(GM soybean) sera was not observed when compared to that by anti-(non-GM soybean) sera. The present results indicate that the GM soybean might not act as a strong allergen in male Sprague Dawley rats.

Spatial-frequency and contrast properties of crowding.

Crowding, the difficulty in recognizing a letter flanked by other letters, has been explained as a lateral masking effect. The purpose of this study was to examine the spatial-frequency and contrast dependencies of crowding, and to compare them with the properties of pattern masking. In experiment 1, we measured contrast thresholds for identifying the middle letters in strings of three randomly chosen lower-case letters (trigrams), for a range of letter spacings. Letters were digitally filtered using a set of bandpass filters, with peak object spatial frequencies ranging from 0.63 to 10 c/letter. Bandwidth of the filters was 1 octave. Frequencies of the target and flanking letters were the same, or differed by up to 2 octaves. Contrast of the flanking letters was fixed at the maximum value. Testing was conducted at the fovea and 5 degrees eccentricity. We found that crowding exhibits spatial-tuning functions like masking, but with generally broader bandwidths than those for masking. The spatial extent of crowding was found to be about 0.5 deg at the fovea and 2 deg at 5 degrees eccentricity, independent of target letter frequency. In experiment 2, we measured the contrast thresholds for identifying the middle target letters in trigrams for a range of flanking letter contrasts at 5 degrees eccentricity. At low flanker contrast, crowding does not show a facilitatory region, unlike pattern masking. At high flanker contrast, threshold rises with contrast with an exponent of 0.13-0.3, lower than corresponding exponents for pattern masking. In experiment 3, we varied the contrast ratio between the flanking letters and the target letters, and found that the magnitude of crowding increases monotonically with contrast ratio. This finding contradicts a prediction based on a grouping explanation for crowding. Our results are consistent with the postulation that crowding and masking may share the same first stage linear filtering process, and perhaps a similar second-stage process, with the additional property that the second-stage process in crowding pools information over a spatial extent that varies with eccentricity.

Psychophysics of reading. XX. Linking letter recognition to reading speed in central and peripheral vision.

Our goal is to link spatial and temporal properties of letter recognition to reading speed for text viewed centrally or in peripheral vision. We propose that the size of the visual span - the number of letters recognizable in a glance - imposes a fundamental limit on reading speed, and that shrinkage of the visual span in peripheral vision accounts for slower peripheral reading. In Experiment 1, we estimated the size of the visual span in the lower visual field by measuring RSVP (rapid serial visual presentation) reading times as a function of word length. The size of the visual span decreased from at least 10 letters in central vision to 1.7 letters at 15 degrees eccentricity, in good agreement with the corresponding reduction of reading speed measured by Chung and coworkers (Chung, S. T. L., Mansfield, J. S., & Legge, G. E. (1998). Psychophysics of reading. XVIII. The effect of print size on reading speed in normal peripheral vision. Vision Research, 38, 2949-2962). In Exp. 2, we measured letter recognition for trigrams (random strings of three letters) as a function of their position on horizontal lines passing through fixation (central vision) or displaced downward into the lower visual field (5, 10 and 20 degrees ). We also varied trigram presentation time. We used these data to construct visual-span profiles of letter accuracy versus letter position. These profiles were used as input to a parameter-free model whose output was RSVP reading speed. A version of this model containing a simple lexical-matching rule accounted for RSVP reading speed in central vision. Failure of this version of the model in peripheral vision indicated that people rely more on lexical inference to support peripheral reading. We conclude that spatiotemporal characteristics of the visual span limit RSVP reading speed in central vision, and that shrinkage of the visual span results in slower reading in peripheral vision.

Elevation of Vernier thresholds during image motion depends on target configuration.

Previously we showed that thresholds for abutting Vernier targets are unaffected by motion, as long as the targets are processed by the same spatial-frequency channel at each velocity and remain equally detectable [Invest. Ophthalmol. Visual Sci. (Suppl.) 37, S734 (1996)]. In this study we compared Vernier thresholds for stationary and moving abutting and nonabutting targets (gaps = 0, 18, and 36 arc min) for velocities of 0-16 deg/s. The Vernier targets were spatially filtered vertical lines (peak spatial frequency = 3.3 or 6.6 c/deg), presented at contrast levels of two, four, and eight times the detection threshold of each component line. Unlike the results for abutting targets, Vernier thresholds for nonabutting targets worsen with velocity as well as gap size. The results for abutting Vernier targets are consistent with the hypothesis that thresholds are mediated by oriented spatial filters, whose responses increase proportionally with the stimulus contrast. The velocity-dependent thresholds found for nonabutting Vernier targets can be explained on the basis of local-sign comparisons if the comparison process is assumed to include a small amount of temporal noise.

Reading with a head-mounted video magnifier.

PURPOSE: This study compared the effectiveness of a head-mounted video magnifier, low-vision enhancement system (LVES), with closed-circuit TV (CCTV) and large print as a device or means of improving reading performance in people with low vision. METHODS: The reading performance of ten low-vision participants was assessed in two ways: (1) By measuring reading speed as a function of print size with LVES and without LVES, and (2) by comparing reading speed and comprehension of news articles using the LVES vs. a popular non-head-mounted video magnifier, the CCTV. RESULTS: Maximum reading speeds with LVES matched the maximum reading speeds with unaided vision attained by enlarging print. The critical print size (the smallest print size that could be read at maximum reading speed) improved significantly for all participants using LVES compared with unaided vision. When comparing reading performance using LVES and CCTV, we found that reading speed and comprehension for the two conditions were equivalent. The two low-vision participants with lowest acuities (20/640 and 20/960) could not read the 10-point newspaper articles with LVES, even with an 8 D auxiliary reading lens that permitted a very close reading distance. CONCLUSIONS: Head-mounted video magnifiers, such as LVES, can support good low-vision reading performance, but the restricted range of magnification may limit the usefulness of the device as a reading magnifier for people with very low acuity.

Curcumin causes the growth arrest and apoptosis of B cell lymphoma by downregulation of egr-1, c-myc, bcl-XL, NF-kappa B, and p53.

It has been well known that curcumin is a powerful inhibitor of proliferation of several tumor cells. However, the molecular basis of the anti-proliferative effect of curcumin has not been investigated in detail. In this paper, we present evidence to show that curcumin inhibited proliferation of a variety of B lymphoma cells. At low concentrations curcumin inhibited the proliferation of BKS-2, an immature B cell lymphoma, more effectively than that of normal B lymphocytes and caused the apoptosis of BKS-2 cells in a dose- and time-dependent manner. Furthermore, curcumin downregulated the expression of survival genes egr-1, c-myc, and bcl-X(L) as well as the tumor suppressor gene p53 in B cells. In addition, NF-kappaB binding activity was also downregulated almost completely by curcumin. Stimulation with CpG oligonucleotides or anti-CD40 overcame growth inhibition induced by low concentrations of curcumin. Our results suggest that curcumin caused the growth arrest and apoptosis of BKS-2 immature B cell lymphoma by downregulation of growth and survival promoting genes.

Determination of melatonin in biological samples by capillary electrophoresis.

The determination of melatonin (MLT) in physiological samples was investigated using capillary electrophoresis (CE). Mouse blood was collected in tubes containing EDTA, centrifuged at 1500 g for 20 min at 4 degrees C, and stored at -20 degrees C. Plasma samples were extracted with dichloroethane, centrifuged and the aqueous phase was discarded. Then the organic phase was evaporated to dryness. The residue was dissolved in deionized water and filtered with a microfilter (0.22 micron). Separations were carried out using a CE system equipped with a fused silica capillary [80 cm (effective length 52 cm) x 75 microns I.D.] and an ultraviolet-visible detector (200 nm), and programmed to provide 25 mM 2-(N-morpholino)ethanesulfonic acid (pH 5.7). Injection was performed hydrostatically by elevating the sample by 10 cm at the cathodic side of the capillary. The calibration curve, reproducibility, recovery and limit of detection were examined, and validation of the method was performed. The result showed that MLT in blood could be easily determined with the new method.

CpG oligodeoxynucleotides rescue BKS-2 immature B cell lymphoma from anti-IgM-mediated growth inhibition by up-regulation of egr-1.

Cross-linking of the IgM antigen receptor on an immature B cell lymphoma (BKS-2) induces growth arrest and apoptosis. This is accompanied by down-regulation of the immediate early genes, egr-1 and c-myc, and a reduction in NF-kappaB activity. Anti-IgM-induced growth arrest and apoptosis of this murine B cell lymphoma were prevented by oligodeoxynucleotides (ODN) containing the CpG motif, which are also known to be stimulatory for mature and immature B cells. The CpG but not non-CpG ODN rescued BKS-2 cells from anti-IgM-mediated growth inhibition by up-regulation of egr-1 and c-myc expression as well as by restoring NF-kappaB activity. Interestingly, changes in egr-1 expression occurred more rapidly than in c-myc expression. Also the c-myc levels remained high up to 6 h after addition of the anti-IgM, which was also the time until which the addition of CpG could be delayed without affecting its ability to provide complete protection. This CpG-induced rescue of B lymphoma cells was blocked by antisense egr-1 ODN, suggesting that the expression of egr-1 is important for the effects of CpG ODN on the growth and survival of BKS-2 cells.

Phototoxicity of melatonin.

Melatonin (MLT), N-acetyl-5-methoxytryptamine, is mainly secreted by the pineal gland. The ultraviolet (UV), infrared (IR) and 1H-NMR spectra of irradiated and non-irradiated MLT were measured, and phototoxicity tests of MLT, anthracene (positive control) and sodium lauryl sulfate (SLS, negative control) were performed. The methods employed include both in vitro tests such as MTS assay using the human fibroblast cell and yeast growth inhibition assay using Candida albicans and in vivo method using the skin of guinea pig. UV absorption spectra and 1H-NMR spectra of MLT were changed by UVA (365 nm, 15 J/cm2), but IR spectra of MLT were not changed. The fifty percent inhibitor concentration (IC50) ratio (UV-/UV+) of MLT was 10. The inhibition zone of irradiated-paper disks treated with MLT was not observed. According to the results of histopathological examination, no pathologic lesion was observed in the non-irradiated group, but slight degeneration of keratinocytes in the epidermis, hemorrhage and vasodilation in dermis were observed in the irradiated group. These results indicate that the molecular structure of MLT is altered by UVA to unidentified photoproducts and a moderate phototoxicity of MLT is predicted.

Comparison of letter and Vernier acuities with dioptric and diffusive blur.

We assessed the influence of dioptric and diffusive blur on normal subjects' letter and Vernier acuity in two experiments. In the first experiment, letter acuity was measured for isolated black Sloan letters and Vernier acuity was determined for a pair of black vertical abutting or nonabutting lines. Targets were viewed through plus lenses that produced 0, 1, 2, 4, and 8 D of dioptric blur. In the second experiment, letter acuity was determined for bright 4-position Ts and Vernier acuity was measured for a pair of bright abutting vertical lines. Six levels of imposed diffusive blur were produced by varying the distance between a ground glass screen and the oscilloscope on which the targets were presented. The results of both experiments indicate that letter and Vernier acuity for abutting or closely separated lines worsen in parallel curvilinear fashion, as long as the lines comprising the Vernier targets remain equally detectable when various amounts of dioptric and diffusive blur are imposed. We conclude that both dioptric and diffusive blur introduce common processing limitations for letter and Vernier acuity.

Effect of yellow filters on pupil size.

The purpose of this study was to investigate the size of the pupil while viewing through yellow and neutral density (ND) filters. Previous studies have shown that the pupil of the human eye is relatively more sensitive to short wavelengths than indicated by the photopic luminosity curve. We first measured the consensual horizontal pupil diameter of 11 observers as a function of luminance (0.144 to 18,150 cd/m2) to establish the luminance-response function for each observer. We then measured the pupil diameter while the observer viewed through a Corning Photochromic Filter (CPF) 550 lens and two ND filters (ND 0.5 and 1.0). The pupil diameters obtained with each filter were compared to the diameters at an equivalent luminance based upon each observer's luminance-response function. Our results show that the pupil diameter is larger with the yellow lens than when viewing a broad spectrum white field at an equivalent luminance. We speculate that our results may explain some, but not all, of the well-known subjective brightness enhancement that occurs when viewing through yellow filters.

Eosinophilic pustular folliculitis (Ofuji's disease) in myelodysplastic syndrome.

We describe a case of eosinophilic pustular folliculitis (EPF, Ofuji's disease) in a 12-year-old male who suffered from myelodysplastic syndrome. Bone marrow study revealed an increase in the eosinophil cell line without peripheral blood eosinophilia in our case. We suggest that the immunologic abberations ascribed to myelodysplastic syndrome and the increase in the eosinophil cell line in the bone marrow might play roles in the development of EPF in our case.

Vernier and letter acuities for low-pass filtered moving stimuli.

Vernier and letter acuities are both susceptible to degradation by image motion. In a previous study, we showed that the worsening of Vernier acuity for stimuli moving up to 4 degrees/s is accounted for primarily by a shift of visual sensitivity to mechanisms of lower spatial frequency. The purposes of this study were to extend the previous results for Vernier acuity to higher stimulus contrast and velocities, and to determine if a shift in spatial scale can similarly explain the degradation of letter acuity for moving stimuli. We measured Vernier discrimination for a pair of vertical abutting thin lines and letter resolution for a four-orientation letter 'T' as a function of stimulus velocity ranging from 0 to 12 degrees/s. Stimuli were presented at 20 times the detection threshold, determined for each velocity. To determine the spatial-frequency mechanism that mediates each task at each velocity, we measured Vernier and letter acuities with low-pass filtered stimuli (cut-off spatial-frequency: 17.1-1.67 c/deg) and analyzed the data using an equivalent blur analysis. Our results show that the empirically determined, equivalent intrinsic blur associated with both tasks increases as a function of stimulus velocity, suggesting corresponding increases in the size of optimally responding mechanisms. This progressive increase in mechanism size can account for the worsening of Vernier and letter acuities with velocity. Vernier discrimination is found to be more susceptible to degradation by various stimulus parameters than letter resolution, suggesting that different mechanisms are involved in the two tasks. We conclude that the elevations in Vernier and letter acuities for moving stimuli are the consequence of a shift of visual sensitivity toward mechanisms of lower spatial frequencies.

Psychophysics of reading. XVIII. The effect of print size on reading speed in normal peripheral vision.

Reading in peripheral vision is slow and requires large print, posing substantial difficulty for patients with central scotomata. The purpose of this study was to evaluate the effect of print size on reading speed at different eccentricities in normal peripheral vision. We hypothesized that reading speeds should remain invariant with eccentricity, as long as the print is appropriately scaled in size--the scaling hypothesis. The scaling hypothesis predicts that log-log plots of reading speed versus print size exhibit the same shape at all eccentricities, but shift along the print-size axis. Six normal observers read aloud single sentences (approximately 11 words in length) presented on a computer monitor, one word at a time, using rapid serial visual presentation (RSVP). We measured reading speeds (based on RSVP exposure durations yielding 80% correct) for eight print sizes at each of six retinal eccentricities, from 0 (foveal) to 20 deg in the inferior visual field. Consistent with the scaling hypothesis, plots of reading speed versus print size had the same shape at different eccentricities: reading speed increased with print size, up to a critical print size and was then constant at a maximum reading speed for larger print sizes. Also consistent with the scaling hypothesis, the plots shifted horizontally such that average values of the critical print size increased from 0.16 deg (fovea) to 2.22 deg (20 deg peripheral). Inconsistent with the scaling hypothesis, the plots also exhibited vertical shifts so that average values of the maximum reading speed decreased from 807 w.p.m. (fovea) to 135 w.p.m. (20 deg peripheral). Because the maximum reading speed is not invariant with eccentricity even when the print size was scaled, we reject the scaling hypothesis and conclude that print size is not the only factor limiting maximum reading speed in normal peripheral vision.

A new silent magnetic resonance imaging using a rotating DC gradient.

A new approach to silent MR imaging using a rotating DC gradient has been explored and experimentally studied. Acoustic or sound noise has been one of the problems in examining patients, mainly due to the fast gradient pulsings in interaction with the main magnetic field. The sound noise has been noted to be proportionately louder as the magnetic field strength becomes larger. In this report, we describe a new imaging technique using a mechanically rotating DC gradient coil. The rotating DC gradient coil can effectively replace both phase encoding as well as readout gradient pulsings, and data obtained in this manner can provide a set of projection data that later can be used for projection reconstruction. With some interpolation techniques one can also perform conventional two-dimensional fast Fourier transform image reconstruction. The sound noise intensity compared with the conventional imaging technique, such as the spin-echo sequence, has been reduced down to about -20.7 dB or 117.5 times with this new technique. The experimental pulse sequence and its principle are described and images obtained by the new silent MR imaging technique are reported.

Moving vernier in amblyopic and peripheral vision: greater tolerance to motion blur.

The purpose of this study was to examine the hypothesis that higher stimulus velocities could be tolerated in amblyopic and normal peripheral vision. The basis for this hypothesis is that a shift in the spatial scale of processing appears to account for the degradation in vernier acuity for moving stimuli in normal vision, and, to a large degree for the degradation in vernier acuity for stationary stimuli in amblyopic and peripheral vision. Vernier thresholds were determined using a pair of long abutting lines, for velocities ranging between 0 and 8 deg/sec. Comparisons were made between non-amblyopic and amblyopic eyes in two amblyopic observers, and between central and peripheral (5 and 10 deg) vision in two normal observers. We analyzed our threshold vs velocity data using an equivalent noise analysis, and defined the knee of the function, the point at which vernier threshold is elevated by a factor of square root of 2, as the "critical velocity" beyond which image motion degrades vernier acuity. Critical velocities were found to be higher in amblyopic than in nonamblyopic eyes; and higher in peripheral than central vision. Our results are consistent with the predictions from the shift in spatial scale notion--that higher velocity of image motion can be tolerated because of the shift in sensitivity toward lower spatial-frequency filter mechanisms in amblyopic and normal peripheral vision.

Congenital nystagmus image motion: influence on visual acuity at different luminances.

In persons with congenital nystagmus (CN), the ability to integrate visual information over time can be limited by two factors--the duration of foveation periods and the temporal integration period of the visual system. The purpose of this study was to assess the relative importance of these two factors for visual acuity for targets of different luminances. We measured visual acuity using Landolt C targets at 5 luminance levels (50 to 0.005 cd/m2) in 6 observers with CN, and in 6 normal observers with comparable motion of the retinal image. To allow comparison, normal observers viewed the targets during image motion simulating jerk CN, with "foveation durations" ranging from 20 to 160 ms. In the normal observers, acuity improves as a function of the simulated foveation duration at all luminance levels. However, this improvement is larger and occurs at a faster rate at high than at low luminances. The more gradual improvement in acuity with simulated foveation durations at low luminances is consistent with a prolongation of the temporal integration period, which we estimate to range from approximately 140 to 380 ms over the 4 log unit range in luminance that we tested. In observers with CN, the change in acuity with luminance is similar, but not identical, to that in normal observers when the duration of the foveation periods is matched. We conclude that the integration of visual information may be limited by either the period of temporal integration or the duration of the foveation period in persons with CN, depending upon which is shorter at the luminance level under consideration.