Backward Masking as a Test of Magnocellular Sensitivity

REFERENCES

• Hendry SH, Reid RC. The koniocellular pathway in primate vision. Annu Rev Neurosci 2000;23:127–153.
   PubMed Web of Science ®Google Scholar
• Merigan WH, Maunsell JH. How parallel are the primate visual pathways? Annu Rev Neurosci 1993;16:369–402.
   PubMed Web of Science ®Google Scholar
• Shapley R, Perry VH. Cat and monkey retinal ganglion cells and their visual functional roles. Trends Neurosci 1986;9:229–235.
   Web of Science ®Google Scholar
• Skottun BC, Skoyles JR. Vernier acuity as a test of magnocellular sensitivity. Neuro-Ophthalmology 2010; 34:82–87.
   Web of Science ®Google Scholar
• Skottun BC, Skoyles JR. Stereopsis and magnocellular sensitivity in schizophrenia. World J Biol Psychiatry 2009;10:697–701.
   PubMed Web of Science ®Google Scholar
• Butler PD, DeSanti LA, Maddox J, Harkavy-Friedman JM, Amador XF, Goetz RR, Javitt DC, Gorman JM. Visual backward-masking deficits in schizophrenia: relationship to visual pathway function and symptomatology. Schizophr Res 2003;59:199–209.
   PubMed Web of Science ®Google Scholar
• Butler PD, Javitt DC. Early-stage visual processing deficits in schizophrenia. Curr Opin Psychiatry 2005;18:151–157.
   PubMed Web of Science ®Google Scholar
• Green MF, Nuechterlein KH, Mintz J. Backward masking in schizophrenia and mania. II. Specifying the visual channels. Arch Gen Psychiatry 1994;51:945–951.
   PubMed Web of Science ®Google Scholar
• Edwards VT, Hogben JH, Clark CD, Pratt C. Effects of a red background on magnocellular functioning in average and specifically disabled readers. Vision Res 1996;36:1037–1045.
   PubMed Web of Science ®Google Scholar
• Levitt JB, Schumer RA, Sherman SM, Spear PD, Movshon JA. Visual response properties of neurons in the LGN of normally reared and visually deprived macaque monkeys. J Neurophysiol 2001;85:2111–2129.
   PubMed Web of Science ®Google Scholar
• Marrocco RT. Sustained and transient cells in monkey lateral geniculate nucleus: conduction velocities and response properties. J Neurophysiol 1976;39:340–353.
   PubMedGoogle Scholar
• Maunsell JH, Gibson JR. Visual response latencies in striate cortex of the macaque monkey. J Neurophysiol 1992;68:1332–1344.
   PubMed Web of Science ®Google Scholar
• Schmolesky MT, Wang Y, Hanes DP, Thompson KG, Leutgeb S, Schall JD, Leventhal AG. Signal timing across the macaque visual system. J Neurophysiol 1998;79:3272–3278.
   PubMed Web of Science ®Google Scholar
• Schroeder CE, Tenke CE, Arezzo JC, Vaughan HG Jr. Timing and distribution of flash-evoked activity in the lateral geniculate nucleus of the alert monkey. Brain Res 1989;477:183–195.
   PubMedGoogle Scholar
• Nowak LG, Bullier J, The timing of information transfer in the visual system. In Rockland K, Kaas J, Peters A, editors. Cerebral Cortex. New York: Plenum, 1997;204–241.
   Google Scholar
• Breitmeyer BG, Ganz L. Implications of sustained and transient channels for theories of visual pattern masking, saccadic suppression, and information processing. Psychol Rev 1976;83:1–36.
   PubMed Web of Science ®Google Scholar
• Weisstein N, Ozog G, Szoc R. A comparison and elaboration of two models of metacontrast. Psychol Rev 1975;82:325–343.
   PubMed Web of Science ®Google Scholar
• Breitmeyer BG, Ogmen H. Recent models and findings in visual backward masking: a comparison, review, and update. Percept Psychophys 2000;62:1572–1595.
   PubMed Web of Science ®Google Scholar
• Ogmen H, Breitmeyer BG, Todd S, Mardon L. Target recovery in metacontrast: the effect of contrast. Vision Res 2006;46:4726–4734.
   PubMed Web of Science ®Google Scholar
• Lefton LA. Metacontrast: a review. Percept Psychophys 1973;13:161–171.
   Web of Science ®Google Scholar
• Alpern M. Metacontrast. J Opt Soc Am 1953;43:648–657.
   PubMed Web of Science ®Google Scholar
• Werner H. Studies on contour: i. Qualitative analysis. Am J Psychol 1935;47:40–64.
   Google Scholar
• Ahmad A, Spear PD. Effects of aging on the size, density, and number of rhesus monkey lateral geniculate neurons. J Comp Neurol 1993;334:631–643.
   PubMed Web of Science ®Google Scholar
• Peters A, Payne BR, Budd J. A numerical analysis of the geniculocortical input to striate cortex in the monkey. Cereb Cortex 1994;4:215–229.
   PubMed Web of Science ®Google Scholar
• Maunsell JH, Ghose GM, Assad JA, McAdams CJ, Boudreau CE, Noerager BD. Visual response latencies of magnocellular and parvocellular LGN neurons in macaque monkeys. Vis Neurosci 1999;16:1–14.
   PubMed Web of Science ®Google Scholar
• Skottun BC. On the use of metacontrast to assess magnocellular function in dyslexic readers. Percept Psychophys 2001;63:1271–1274.
   PubMed Web of Science ®Google Scholar
• Skottun BC, Skoyles JR. Metacontrast, target recovery, and the magno- and parvocellular systems: a perspective. Vis Neurosci 2007;24:177–181.
   PubMed Web of Science ®Google Scholar
• Ogmen H, Purushothaman G, Breitmeyer BG. Metacontrast, target recovery, and the magno- and parvocellular systems: a reply to the perspective. Vis Neurosci 2008;25:611–616.
   PubMed Web of Science ®Google Scholar
• Dreher B, Fukada Y, Rodieck RW. Identification, classification and anatomical segregation of cells with X-like and Y-like properties in the lateral geniculate nucleus of old-world primates. J Physiol 1976;258:433–452.
   PubMed Web of Science ®Google Scholar
• Blakemore C, Vital-Durand F. Organization and post-natal development of the monkey’s lateral geniculate nucleus. J Physiol 1986;380:453–491.
   PubMed Web of Science ®Google Scholar
• Kaplan E, Shapley RM. X and Y cells in the lateral geniculate nucleus of macaque monkeys. J Physiol 1982;330:125–143.
   PubMed Web of Science ®Google Scholar
• Gielen C. Spatio-temporal and chromatic properties of visual neurones in the rhesus monkey geniculate nucleus. Nijmegen, The Netherlands: University of Nijmegen, 1980.
   Google Scholar
• Kaplan E, Shapley RM. The primate retina contains two types of ganglion cells, with high and low contrast sensitivity. Proc Natl Acad Sci U S A 1986;83:2755–2757.
   PubMed Web of Science ®Google Scholar
• Kilavik BE, Silveira LC, Kremers J. Spatial receptive field properties of lateral geniculate cells in the owl monkey (Aotus azarae) at different contrasts: a comparative study. Eur J Neurosci 2007;26:992–1006.
   PubMedGoogle Scholar
• White AJ, Solomon SG, Martin PR. Spatial properties of koniocellular cells in the lateral geniculate nucleus of the marmoset Callithrix jacchus. J Physiol 2001;533:519–535.
   PubMed Web of Science ®Google Scholar
• Sclar G, Maunsell JH, Lennie P. Coding of image contrast in central visual pathways of the macaque monkey. Vision Res 1990;30:1–10.
   PubMed Web of Science ®Google Scholar
• Skottun BC, Bradley A, Freeman RD. Orientation discrimination in amblyopia. Invest Ophthalmol Vis Sci 1986;27:532–537.
   PubMedGoogle Scholar
• Skottun BC, Bradley A, Sclar G, Ohzawa I, Freeman RD. The effects of contrast on visual orientation and spatial frequency discrimination: a comparison of single cells and behavior. J Neurophysiol 1987;57:773–786.
   PubMed Web of Science ®Google Scholar
• Hubel DH, Wiesel TN. Receptive fields and functional architecture of monkey striate cortex. J Physiol 1968;195:215–243.
   PubMed Web of Science ®Google Scholar
• Miki A, Siegfried JB, Liu C-SJ Modestino, EJ, Liu GT. Magno- and parvocellular visual cortex activation in anisometropic amblyopia, as studied with functional magnetic resonance imaging. Neuro-Ophthalmology 2008;32:187–189.
   Web of Science ®Google Scholar
• Skottun BC, Skoyles JR. The parvocellular system in amblyopia. Neuro-Ophthalmology 2008;32:177–178.
   Web of Science ®Google Scholar