Analog Numerical Representations in Rhesus Monkeys: Evidence for Parallel Processing

2004 ◽  
Vol 16 (5) ◽  
pp. 889-901 ◽  
Author(s):  
Andreas Nieder ◽  
Earl K. Miller

Monkeys have been introduced as model organisms to study neural correlates of numerical competence, but many of the behavioral characteristics of numerical judgments remain speculative. Thus, we analyzed the behavioral performance of two rhesus monkeys judging the numerosities 1 to 7 during a delayed match-to-sample task. The monkeys showed similar discrimination performance irrespective of the exact physical appearance of the stimuli, confirming that performance was based on numerical information. Performance declined smoothly with larger numerosities, and reached discrimination threshold at numerosity “4.” The nonverbal numerical representations in monkeys were based on analog magnitudes, object tracking process (“subitizing”) could not account for the findings because the continuum of small and large numbers shows a clear Weber fraction signature. The lack of additional scanning eye movements with increasing set sizes, together with indistinguishable neuronal response latencies for neurons with different preferred numerosities, argues for parallel encoding of numerical information. The slight but significant increase in reaction time with increasing numerosities can be explained by task difficulty and consequently time-consuming decision processes. The behavioral results are compared to single-cell recordings from the prefrontal cortex in the same subjects. Models for numerosity discrimination that may account for these results are discussed.

2016 ◽  
Vol 283 (1827) ◽  
pp. 20160083 ◽  
Author(s):  
Helen M. Ditz ◽  
Andreas Nieder

The ability to estimate number is widespread throughout the animal kingdom. Based on the relative close phylogenetic relationship (and thus equivalent brain structures), non-verbal numerical representations in human and non-human primates show almost identical behavioural signatures that obey the Weber–Fechner law. However, whether numerosity discriminations of vertebrates with a very different endbrain organization show the same behavioural signatures remains unknown. Therefore, we tested the numerical discrimination performance of two carrion crows ( Corvus corone ) to a broad range of numerosities from 1 to 30 in a delayed match-to-sample task similar to the one used previously with primates. The crows' discrimination was based on an analogue number system and showed the Weber-fraction signature (i.e. the ‘just noticeable difference’ between numerosity pairs increased in proportion to the numerical magnitudes). The detailed analysis of the performance indicates that numerosity representations in crows are scaled on a logarithmically compressed ‘number line’. Because the same psychophysical characteristics are found in primates, these findings suggest fundamentally similar number representations between primates and birds. This study helps to resolve a classical debate in psychophysics: the mental number line seems to be logarithmic rather than linear, and not just in primates, but across vertebrates.


2020 ◽  
Vol 123 (1) ◽  
pp. 134-148
Author(s):  
Boris Gourévitch ◽  
Elena J. Mahrt ◽  
Warren Bakay ◽  
Cameron Elde ◽  
Christine V. Portfors

Speech is our most important form of communication, yet we have a poor understanding of how communication sounds are processed by the brain. Mice make great model organisms to study neural processing of communication sounds because of their rich repertoire of social vocalizations and because they have brain structures analogous to humans, such as the auditory midbrain nucleus inferior colliculus (IC). Although the combined roles of GABAergic and glycinergic inhibition on vocalization selectivity in the IC have been studied to a limited degree, the discrete contributions of GABAergic inhibition have only rarely been examined. In this study, we examined how GABAergic inhibition contributes to shaping responses to pure tones as well as selectivity to complex sounds in the IC of awake mice. In our set of long-latency neurons, we found that GABAergic inhibition extends the evoked firing rate range of IC neurons by lowering the baseline firing rate but maintaining the highest probability of firing rate. GABAergic inhibition also prevented IC neurons from bursting in a spontaneous state. Finally, we found that although GABAergic inhibition shaped the spectrotemporal response to vocalizations in a nonlinear fashion, it did not affect the neural code needed to discriminate vocalizations, based either on spiking patterns or on firing rate. Overall, our results emphasize that even if GABAergic inhibition generally decreases the firing rate, it does so while maintaining or extending the abilities of neurons in the IC to code the wide variety of sounds that mammals are exposed to in their daily lives. NEW & NOTEWORTHY GABAergic inhibition adds nonlinearity to neuronal response curves. This increases the neuronal range of evoked firing rate by reducing baseline firing. GABAergic inhibition prevents bursting responses from neurons in a spontaneous state, reducing noise in the temporal coding of the neuron. This could result in improved signal transmission to the cortex.


2006 ◽  
Vol 18 (5) ◽  
pp. 737-748 ◽  
Author(s):  
Valentin Dragoi ◽  
Mriganka Sur

It is generally believed that the visual system is adapted to the statistics of the visual world. Measuring and understanding these statistics require precise knowledge of the structure of the signals reaching fovea during image scanning. However, despite the fact that eye movements cause retinal stimulation to change several times in a second, it is implicitly assumed that images are sampled uniformly during natural viewing. By analyzing the eye movements of three rhesus monkeys freely viewing natural scenes, we report here significant anisotropy in stimulus statistics at the center of gaze. We find that fixation on an image patch is more likely to be followed by a saccade to a nearby patch of similar orientation structure or by a saccade to a more distant patch of largely dissimilar orientation structure. Furthermore, we show that orientation-selective neurons in the primary visual cortex (V1) can take advantage of eye movement statistics to selectively improve their discrimination performance.


2010 ◽  
Vol 104 (5) ◽  
pp. 2500-2511 ◽  
Author(s):  
Mary F. Howard ◽  
David Poeppel

Speech stimuli give rise to neural activity in the listener that can be observed as waveforms using magnetoencephalography. Although waveforms vary greatly from trial to trial due to activity unrelated to the stimulus, it has been demonstrated that spoken sentences can be discriminated based on theta-band (3–7 Hz) phase patterns in single-trial response waveforms. Furthermore, manipulations of the speech signal envelope and fine structure that reduced intelligibility were found to produce correlated reductions in discrimination performance, suggesting a relationship between theta-band phase patterns and speech comprehension. This study investigates the nature of this relationship, hypothesizing that theta-band phase patterns primarily reflect cortical processing of low-frequency (<40 Hz) modulations present in the acoustic signal and required for intelligibility, rather than processing exclusively related to comprehension (e.g., lexical, syntactic, semantic). Using stimuli that are quite similar to normal spoken sentences in terms of low-frequency modulation characteristics but are unintelligible (i.e., their time-inverted counterparts), we find that discrimination performance based on theta-band phase patterns is equal for both types of stimuli. Consistent with earlier findings, we also observe that whereas theta-band phase patterns differ across stimuli, power patterns do not. We use a simulation model of the single-trial response to spoken sentence stimuli to demonstrate that phase-locked responses to low-frequency modulations of the acoustic signal can account not only for the phase but also for the power results. The simulation offers insight into the interpretation of the empirical results with respect to phase-resetting and power-enhancement models of the evoked response.


1999 ◽  
Vol 82 (3) ◽  
pp. 1651-1654 ◽  
Author(s):  
Dora E. Angelaki ◽  
M. Quinn McHenry

Short-lasting, transient head displacements and near target fixation were used to measure the latency and early response gain of vestibularly evoked eye movements during lateral and fore-aft translations in rhesus monkeys. The latency of the horizontal eye movements elicited during lateral motion was 11.9 ± 5.4 ms. Viewing distance-dependent behavior was seen as early as the beginning of the response profile. For fore-aft motion, latencies were different for forward and backward displacements. Latency averaged 7.1 ± 9.3 ms during forward motion (same for both eyes) and 12.5 ± 6.3 ms for the adducting eye (e.g., left eye during right fixation) during backward motion. Latencies during backward motion were significantly longer for the abducting eye (18.9 ± 9.8 ms). Initial acceleration gains of the two eyes were generally larger than unity but asymmetric. Specifically, gains were consistently larger for abducting than adducting eye movements. The large initial acceleration gains tended to compensate for the response latencies such that the early eye movement response approached, albeit consistently incompletely, that required for maintaining visual acuity during the movement. These short-latency vestibuloocular responses could complement the visually generated optic flow responses that have been shown to exhibit much longer latencies.


2011 ◽  
Vol 106 (3) ◽  
pp. 1166-1178 ◽  
Author(s):  
Andres Carrasco ◽  
Stephen G. Lomber

Interactions between living organisms and the environment are commonly regulated by accurate and timely processing of sensory signals. Hence, behavioral response engagement by an organism is typically constrained by the arrival time of sensory information to the brain. While psychophysical response latencies to acoustic information have been investigated, little is known about how variations in neuronal response time relate to sensory signal characteristics. Consequently, the primary objective of the present investigation was to determine the pattern of neuronal activation induced by simple (pure tones), complex (noise bursts and frequency modulated sweeps), and natural (conspecific vocalizations) acoustic signals of different durations in cat auditory cortex. Our analysis revealed three major cortical response characteristics. First, latency measures systematically increase in an antero-dorsal to postero-ventral direction among regions of auditory cortex. Second, complex acoustic stimuli reliably provoke faster neuronal response engagement than simple stimuli. Third, variations in neuronal response time induced by changes in stimulus duration are dependent on acoustic spectral features. Collectively, these results demonstrate that acoustic signals, regardless of complexity, induce a directional pattern of activation in auditory cortex.


2013 ◽  
Vol 109 (2) ◽  
pp. 546-556 ◽  
Author(s):  
Nobuya Sato ◽  
William K. Page ◽  
Charles J. Duffy

We presented optic flow simulating eight directions of self-movement in the ground plane, while monkeys performed delayed match-to-sample tasks, and we recorded dorsal medial superior temporal (MSTd) neuronal activity. Randomly selected sample headings yield smaller test responses to the neuron's preferred heading when it is near the sample's heading direction and larger test responses to the preferred heading when it is far from the sample's heading. Limiting test stimuli to matching or opposite headings suppresses responses to preferred stimuli in both test conditions, whereas focusing on each neuron's preferred vs. antipreferred stimuli enhances responses to the antipreferred stimulus. Match vs. opposite paradigms create bimodal heading profiles shaped by interactions with late delay-period activity. We conclude that task contingencies, determining the prior probabilities of specific stimuli, interact with the monkeys' perceptual strategy for optic flow analysis. These influences shape attentional and working memory effects on the heading direction selectivities and preferences of MSTd neurons.


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