Attractor dynamics of working memory explain a concurrent evolution of stimulus-specific and decision-consistent biases in visual estimation.

IF 15 1区 医学 Q1 NEUROSCIENCES
Hyunwoo Gu, Joonwon Lee, Sungje Kim, Jaeseob Lim, Hyang-Jung Lee, Heeseung Lee, Min Jin Choe, Dong-Gyu Yoo, Jun Hwan Joshua Ryu, Sukbin Lim, Sang-Hun Lee
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引用次数: 0

Abstract

Sensory evidence tends to be fleeting, often unavailable when we categorize or estimate world features. To overcome this, our brains sustain sensory information in working memory (WM). Although keeping that information accurate while acting on it is vital, humans display two canonical biases: estimates are biased toward a few stimuli ("stimulus-specific bias") and prior decisions ("decision-consistent bias"). Integrative-especially neural mechanistic-accounts of these biases remain scarce. Here, we identify drift dynamics toward discrete attractors as a common source of both biases in orientation estimation, with decisions further steering memory states. Behavior and neuroimaging data reveal how these biases co-evolve through the decision-steered attractor dynamics. Task-optimized recurrent neural networks suggest neural mechanisms that enable categorical decisions to emerge from WM for continuous stimuli while updating their trajectory, warping decision-consistent biases under stimulus-specific drift.

工作记忆的吸引子动力学解释了视觉估计中刺激特异性和决策一致性偏差的并发进化。
感官证据往往是短暂的,当我们对世界特征进行分类或估计时,往往是不可用的。为了克服这一点,我们的大脑在工作记忆(WM)中维持感觉信息。尽管在采取行动时保持信息的准确性至关重要,但人类表现出两种典型的偏见:估计偏向于少数刺激(“刺激特异性偏见”)和先前的决定(“决策一致偏见”)。对这些偏见的综合——尤其是神经力学——解释仍然很少。在这里,我们将离散吸引子的漂移动力学识别为方向估计中两种偏差的共同来源,决策进一步指导记忆状态。行为和神经成像数据揭示了这些偏见是如何通过决策导向的吸引子动力学共同进化的。任务优化的递归神经网络提出了一种神经机制,使分类决策能够从连续刺激的WM中出现,同时更新其轨迹,扭曲刺激特异性漂移下的决策一致偏差。
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来源期刊
Neuron
Neuron 医学-神经科学
CiteScore
24.50
自引率
3.10%
发文量
382
审稿时长
1 months
期刊介绍: Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.
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