Dual Deficits in Visual Working Memory Capacity and Filtering Efficiency in Deaf College Students under Higher Load

Chen Ying, Zhou Li, Wang Yan, Pan Qianqian, Liang Yongsheng, Yang Fuyi

Journal of Psychological Science ›› 2025, Vol. 48 ›› Issue (5) : 1062-1075.

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Journal of Psychological Science ›› 2025, Vol. 48 ›› Issue (5) : 1062-1075. DOI: 10.16719/j.cnki.1671-6981.20250504
General Psychology, Experimental Psychology & Ergonomics

Dual Deficits in Visual Working Memory Capacity and Filtering Efficiency in Deaf College Students under Higher Load

  • Chen Ying1, Zhou Li2, Wang Yan3, Pan Qianqian4, Liang Yongsheng5, Yang Fuyi6
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Abstract

More than 80% of human information comes through the visual channel. Visual working memory serves as a resource-limited cognitive system specialized in temporarily storing and processing visual information. Attention involves the selection and allocation of information, with which controlling and regulating the flexible allocation of cognitive resources during information processing. From the perspective of individual differences, research has shown that the performance differences in visual working memory capacity among groups and individuals within groups, which can predict higher cognitive functions such as fluid intelligence and problem-solving, may be related to the efficiency of attention selection, such as filtering out irrelevant information during the encoding.
Early sensory deprivation, such as hearing loss, can profoundly alter brain structure and function. For individuals with profound hearing loss, vision becomes a primary modality for environmental interaction and information acquisition.This population thus offers critical insights into plasticity mechanisms driven by perceptual deprivation. Additionally, prolonged engagement with visual language (e.g., sign language, lip-reading) may exhibit specialized adaptations in visual processing. However, non-verbal visual processing in individuals with hearing loss has received limited scholarly attention. Furthermore, existing empirical evidence remains inconclusive as to whether their visual functions are superior to those of hearing individuals (Compensation Theory), impaired (Deficit Theory), or selectively modulated by environmental demands (Integration Theory). Moreover, little research has focused on the interaction between visual working memory and visual attention between individuals with and without hearing loss. Consequently, whether impairments in VWM capacity and its underlying attention mechanisms(i.e., filtering efficiency) exist in the deaf remain unclear to date.
Using a change detection paradigm, this study examined differences in visual working memory (VWM) capacity and irrelevant stimulus filtering efficiency between deaf and hearing college students. Experiment 1 demonstrated that while the deaf group showed generally reduced VWM capacity, pronounced deficits were observed exclusively under high cognitive load. In Experiment 2, both groups exhibited impaired filtering of task-irrelevant stimuli during encoding, with VWM capacity strongly linked to filtering efficiency. Critically, the deaf group displayed significantly weaker filtering efficiency, and their susceptibility to irrelevant interference intensified proportionally with task demands. In summary, this study reveals a dual pattern in the visual working memory of deaf college students: while their capacity and filtering efficiency markedly decline under high cognitive load compared to hearing peers, the intrinsic coupling between these two metrics remains conserved. These findings align with the Integration Theory, suggesting that visual processing in hearing loss populations reflects both compensatory plasticity and residual constraints of sensory deprivation.

Key words

deaf college students / VWM / capacity / filtering efficiency / integrated hypothesis

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Chen Ying, Zhou Li, Wang Yan, Pan Qianqian, Liang Yongsheng, Yang Fuyi. Dual Deficits in Visual Working Memory Capacity and Filtering Efficiency in Deaf College Students under Higher Load[J]. Journal of Psychological Science. 2025, 48(5): 1062-1075 https://doi.org/10.16719/j.cnki.1671-6981.20250504

References

[1] 高在峰, 郁雯珺, 徐晓甜, 尹军, 水仁德, 沈模卫. (2012). 对侧延迟活动:视觉工作记忆信息存储的ERP指标. 科学通报, 57(30), 2806-2814.
[2] 刘少英, 葛列众, 朱瑶. (2004). 4-6岁幼儿颜色偏好的实验研究. 心理科学, 27(3), 669-670.
[3] 庞超, 陈颜璋, 王莉, 杨喜端, 贺雅, 李芷莹, 欧阳小钰, 傅世敏, 南威治. (2023). 客体信息在视觉工作记忆编码和维持阶段的不同注意选择模式. 心理学报, 55(9), 1397-1410.
[4] 王庭照, 杨鹃, 杨彦平. (2013).工作记忆负荷、形状干扰对聋人与听力正常人注意捕获影响的眼动研究.心理科学, 36(4), 797-801.
[5] 闫国利, 秦钊. (2021). 听觉障碍对聋人视觉功能影响的理论之争: 缺陷还是补偿? 心理科学, 44(5), 1266-1272.
[6] 张萌, 冯建新. (2014). 听力障碍儿童工作记忆的研究进展. 中国特殊教育, 24(6), 37-42.
[7] 张照, 张力为, 龚然. (2021). 视觉工作记忆的过滤效能. 心理科学进展, 29(4), 635-651.
[8] Adam K. C. S., Robison M. K., & Vogel E. K. (2018). Contralateral delay activity tracks fluctuations in working memory performance. Journal of Cognitive Neuroscience, 30(9), 1229-1240.
[9] Baddeley, A. (2013). Working memory: Looking back and looking forward. Nature Reviews Neuroscience, 4(10), 829-839.
[10] Balaban H., Fukuda K., & Luria R. (2019). What can half a million change detection trials tell us about visual working memory? Cognition, 191(10), 103984.
[11] Bao, H. W. S. (2022). bruceR: Broadly useful convenient and efficient R functions. R package version 0.8.x. https://CRAN.R-project.org/package=bruceR
[12] Bates D., Mchler M., Bolker, B. M., & Walker, S. C. (2015). Fitting linear mixed-effects models using lme. https://cran.r-project.org/web/packages/lme4/vignettes/lmer.pdf
[13] Bavelier D., Tomann A., Hutton C., Mitchell T., Corina D., Liu G., & Neville H. (2001). Visual attention to the periphery is enhanced in congenitally deaf individuals. The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, 20(17), RC93.
[14] Böing S., Ten Brink A. F., Hoogerbrugge A. J., Oudman E., Postma A., Nijboer T. C. W., & Van der Stigchel, S. (2023). Eye movements as proxy for visual working memory usage: Increased reliance on the external world in Korsakoff Syndrome. Journal of Clinical Medicine, 12(11), 3630.
[15] Codina C., Pascalis O., Baseler H. A., Levine A. T., & Buckley D. (2017). Peripheral visual reaction time is faster in deaf adults and British sign language interpreters than in hearing adults. Frontiers in Psychology, 8, 50.
[16] Chu, C. Y., Chen, C. A. (2023). Variables related to the executive function in deaf and hard-of-hearing preschoolers. Journal of Developmental and Physical Disabilities, 35, 1-17.
[17] Conway C. M., Pisoni D. B., Kronenberger W. G. (2009). The importance of sound for cognitive sequencing abilities: The auditory scaffolding hypothesis. Current Directions in Psychological Science, 18(5), 275-279.
[18] Conway, A., & Kovacs, K. (2013). Individual differences in intelligence and working memory: A review of latent variable models. Psychology of Learning and Motivation, 58, 233-270.
[19] Cowan, N. (2001). The magical number 4 in short-term memory: A reconsideration of mental storage capacity. Behavioral and Brain Sciences, 24(1), 87-114.
[20] Cowan N., Elliott E. M., Scott S. J., Morey C. C., Mattox S., Hismjatullina A., & Conway, A. R. A. (2005). On the capacity of attention: Its estimation and its role in working memory and cognitive aptitudes. Cognitive Psychology, 51(1), 42-100.
[21] Cusack R., Lehmann M., Veldsman M., & Mitchell D. J. (2009). Encoding strategy and not visual working memory capacity correlates with intelligence. Psychonomic Bulletin and Review, 16(4), 641-647.
[22] Diamond, A. (2013). Executive functions. Annual Review of Psychology, 64(9), 135-168.
[23] Dye, M. W. G., & Bavelier, D. (2010). Attentional enhancements and deficits in deaf populations: An integrative review. Restorative Neurology and Neuroscience, 28(2), 181-192.
[24] Dye, M., & Hauser, P. C. (2014). Sustained attention, selective attention and cognitive control in deaf and hearing children. Hearing Research, 309(3), 94-102.
[25] Engle, R. W. (2002). Working memory capacity as executive attention. Current Directions in Psychological Science, 11, 19-23.
[26] Engle, R. W. (2018). Working memory and executive attention: A revisit perspectives on psychological. Science: A Journal of the Association for Psychological Science, 13(2), 190-193.
[27] Erickson M. A., Hahn B., Leonard C. J., Robinson B., Gray B., Luck S. J., & Gold J. (2015). Impaired working memory capacity is not caused by failures of selective attention in schizophrenia. Schizophrenia Bulletin, 41(2), 366-373.
[28] Forster, S., & Lavie, N. (2008). Failures to ignore entirely irrelevant distractors: The role of load. Journal of Experimental Psychology: Applied, 14(1), 73-83.
[29] Fukuda, K., & Vogel, E. K. (2009). Human variation in overriding attentional capture. The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, 29(27), 8726-8733.
[30] Fukuda K., Vogel E., Mayr U., & Awh E. (2010). Quantity, not quality: The relationship between fluid intelligence and working memory capacity. Psychonomic Bulletin and Review, 17(5), 673-679.
[31] Fukuda, K., & Vogel, E. K. (2011). Individual differences in recovery time from attentional capture. Psychological Science, 22(3), 361-368.
[32] Geraci C., Gozzi M., Papagno C., & Cecchetto C. (2008). How grammar can cope with limited short-term memory: Simultaneity and seriality in sign languages. Cognition, 106(2), 780-804.
[33] Hall M. L., Eigsti I. M., Bortfeld H., & Lillo-Martin D. (2018). Executive function in deaf children: Auditory access and language access. Journal of Speech Language and Hearing Research, 61(8), 1970-1988.
[34] Heimler, B., & Pavani, F. (2014). Response speed advantage for vision does not extend to touch in early deaf adults. Experimental Brain Research, 232(4), 1335-1341.
[35] Jones A., Atkinson J., Marshall C., Botting N., Clair S., M. C., & Morgan G. (2020). Expressive vocabulary predicts nonverbal executive function: A 2-year longitudinal study of deaf and hearing children. Child Development, 91(2), 400-414.
[36] Jost K., Bryck R. L., Vogel E. K., & Mayr U. (2011). Are old adults just like low working memory young adults? Filtering efficiency and age differences in visual working memory. Cerebral Cortex, 21(5), 1147-1154.
[37] Kane, M. J., & Engle, R. W. (2002). The role of prefrontal cortex in working-memory capacity, executive attention, and general fluid intelligence: An individual differences perspective. Psychonomic Bulletin and Review, 9(4), 637-671.
[38] Ku, Y. (2018). Selective attention on representations in working memory: Cognitive and neural mechanisms. PeerJ, 6, e4585.
[39] Lavie, N. (2004). Distracted and confused: Selective attention under load. Trends in Cognitive Sciences, 9(2), 75-82.
[40] Lee E. Y., Cowan N., Vogel E. K., Rolan T., Valle-Inclán F., & Hackley S. A. (2010). Visual working memory deficits in patients with Parkinson's disease are due to both reduced storage capacity and impaired ability to filter out irrelevant information. Brain, 133(9), 2677-2689.
[41] Lee K. R., Groesbeck E., Gwinn O. S., Webster M. A., & Jiang F. (2022). Enhanced peripheral face processing in deaf individuals. Journal of Perceptual Imaging, 5(1), 1-7.
[42] Li, C. H., Xu, H., Wang, Y. J., Zhe, H., & Guo, C. Y. (2017a). Visual working memory capacity can be increased by training on distractor filtering efficiency. Frontiers in Psychology, 8(1748), 196.
[43] Li S., Cai Y., Liu J., Li D., Feng Z., Chen C., & Xue G. (2017b). Dissociated roles of the parietal and frontal cortices in the scope and control of attention during visual working memory. NeuroImage, 149(4), 210-219.
[44] Liu S., Poh J. H., Koh H. L., Ng K. K., Loke Y. M., Lim J. K. W., Chong J. S. X., & Zhou J. (2018). Carrying the past to the future: Distinct brain networks underlie individual differences in human spatial working memory capacity. NeuroImage, 176(8), 1-10.
[45] López-Crespo G., Daza M. T., & Méndez-López M. (2012). Visual working memory in deaf children with diverse communication modes: Improvement by differential outcomes. Research in Developmental Disabilities, 33(2), 362-368.
[46] Luck, S. J., & Vogel, E. K. (1997).The capacity of visual working memory for features and conjunctions. Nature, 390(6657), 279-281.
[47] Luck, S. J., & Vogel, E. K. (2013). Visual working memory capacity: From psychophysics and neurobiology to individual differences. Trends in Cognitive Sciences, 17(8), 391-400.
[48] Mall J. T., Morey C. C., Wolff M. J., & Lehnert F. (2014). Visual selective attention is equally functional for individuals with low and high working memory capacity: Evidence from accuracy and eye movements. Attention, Perception and Psychophysics, 76(7), 1998-2014.
[49] Marjolein S., Vogel E. K., Jonkman L. M., & Katsumi W. (2013). No behavioral or ERP evidence for a developmental lag in visual working memory capacity or filtering in adolescents and adults with ADHD. PLoS ONE, 8(5), e62673.
[50] Marschark M., Sarchet T., & Trani A. (2016). Effects of hearing status and sign language use on working memory. Journal of Deaf Studies and Deaf Education, 21(2), 148-155.
[51] Marshall C., Jones A., Denmark T., Mason K., Atkinson J., Botting N., & Morgan G. (2015). Deaf children's nonverbal working memory is impacted by their language experience. Frontiers in Psychology, 6, 527.
[52] Martin J. D., Tsukahara J. S., Draheim C., Shipstead Z., Mashburn C. A., Vogel E. K., & Engle R. W. (2021). The visual arrays task: Visual storage capacity or attention control? Journal of Experimental Psychology: General, 150(12), 2525-2551.
[53] Masahiro, K., & Yoko, Y. (2012). Individual visual working memory capacities and related brain oscillatory activities are modulated by color preferences. Frontiers in Human Neuroscience, 6(6), 318.
[54] McVay, J. C., & Kane, M. J. (2012). Why does working memory capacity predict variation in reading comprehension? On the influence of mind wandering and executive attention. Journal of Experimental Psychology: General, 141(2), 302-320.
[55] Pavani F.,& Bottari, D. (2012). Visual abilities in individuals with profound deafness a critical review. In M. M. Murray & M. T. Wallace (Eds), The neural bases of multi-sensory processes. (pp.421-445). CRC Press, Taylor & Francis Llc.
[56] Rouder, J. N., Morey, R. D., Morey, C. C., & Cowan, N. (2011). How to measure working memory capacity in the change detection paradigm. Psychonomic Bulletin and Review, 18(2), 324-330.
[57] Shvartsman, M., & Shaul, S. (2023). The role of working memory in early literacy and numeracy skills in kindergarten and first grade. Children (Basel), 10(8), 1285.
[58] Stevenson R. A., Ruppel J., Sun S. Z., Segers M., Zapparoli B. L., Bebko J. M., Barense M. D., & Ferber S. (2021). Visual working memory and sensory processing in autistic children. Scientific Reports, 11(1), 3648.
[59] Stout, D. M., Shackman, A. J., & Larson, C. L. (2013). Failure to filter: Anxious individuals show inefficient gating of threat from working memory. Frontiers in Human Neuroscience, 7(58), 58.
[60] Thakur R., Jayakumar J., & Pant S. (2023). Visual perception and attentional skills in school-age children: A cross-sectional study of reading proficiency in the hearing impaired. Indian Journal of Community Medicine: Official Publication of Indian Association of Preventive and Social Medicine, 48(4), 544-549.
[61] Unsworth N., Fukuda K., Awh E., & Vogel E. K. (2015). Working memory delay activity predicts individual differences in cognitive abilities. Journal of Cognitive Neuroscience, 27(5), 853-865.
[62] Vogel, E. K., & Machizawa, M. G. (2004). Neural activity predicts individual differences in visual working memory capacity. Nature, 428(4), 748-751.
[63] Vogel E. K., McCollough A. W., & Machizawa M. G. (2005). Neural measures reveal individual differences in controlling access to working memory. Nature, 438(11), 500-503.
[64] Xie K., Jin Z., Jin D. G., Zhang J., & Li L. (2022). Shared and distinct structure-function substrates of heterogenous distractor suppression ability between high and low working memory capacity individuals. NeuroImage, 260(10), 119483.
[65] Xu M., Qiao L., Qi S., Li Z., Diao L., Fan L., Zhang L., & Yang D. (2018). Social exclusion weakens storage capacity and attentional filtering ability in visual working memory. Social Cognitive and Affective Neuroscience, 13(1), 92-101.
[66] Ye C., Xu Q., Liu X., Astikainen P., Zhu Y., Hu Z., & Liu Q. (2021). Individual differences in working memory capacity are unrelated to the magnitudes of retrocue benefits. Scientific Reports, 11, Article 7258.
[67] Ye C., Liu R., Guo L., Zhao G., & Liu Q. (2024). A negative emotional state impairs individuals' ability to filter distractors from working memory: An ERP study. Cognitive, Affective and Behavioral Neuroscience, 24(3), 491-504.
[68] Zhao C., Vogel E., & Awh E. (2023). Change localization: A highly reliable and sensitive measure of capacity in visual working memory. Attention, Perception and Psychophysics, 85(5), 1681-1694.
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