Neural Mechanisms of Tactile Texture Perception
Summary and Keywords
The ability to identify tactile objects depends in part on the perception of their surface microstructure and material properties. Texture perception can, on a first approximation, be described by a number of nameable perceptual axes, such as rough/smooth, hard/soft, sticky/slippery, and warm/cool, which exist within a complex perceptual space. The perception of texture relies on two different neural streams of information: Coarser features, measured in millimeters, are primarily encoded by spatial patterns of activity across one population of tactile nerve fibers, while finer features, down to the micron level, are encoded by finely timed temporal patterns within two other populations of afferents. These two streams of information ascend the somatosensory neuraxis and are eventually combined and further elaborated in the cortex to yield a high-dimensional representation that accounts for our exquisite and stable perception of texture.
We can identify objects by the way they feel. As we move our fingers over objects in our pocket or purse, we can easily pick out keys or a phone from an assortment of other items. This ability to identify objects relies in part on the tactile perception of texture (Klatzky, Lederman, & Metzger, 1985). Using touch, we can reliably distinguish satin from silk, or perceive subtle differences between kinds of denim. This extraordinarily rich tactile experience of texture requires the integration of information across a wide span of spatial scales, ranging across six orders of magnitude (from tens of nanometers to tens to millimeters [Skedung et al., 2013]), and gives rise to a complex sensory space that comprises at least four primary perceptual axes—roughness, hardness, stickiness, and warmth (Hollins, Faldowski, Rao, & Young, 1993; Hollins, Bensmaia, Karlof, & Young, 2000a; Picard, Dacremont, Valentin, & Giboreau, 2003; Guest et al., 2011; Okamoto, Nagano, & Yamada, 2013), and many more nameable and unnameable ones.
When fingers run over a surface, the skin is deformed, which in turn results in stresses and strains in the tissue, ultimately driving spatiotemporal patterns of electrical activity in several populations of mechanoreceptors (Sripati, Bensmaia, & Johnson, 2006; Saal, Delhaye, Rayhaun, & Bensmaia, 2017). Patterns on different spatial scales are encoded through parallel mechanisms: Larger spatial patterns of skin deformation (on the order of millimeters) engage spatial encoding mechanisms that suggest compelling analogies with vision (Pack & Bensmaia, 2015; Yau, Hollins, & Bensmaia, 2016), while finer spatial patterns (on the order of microns) drive perceptually relevant skin vibrations (Hollins & Risner, 2000; Bensmaia & Hollins, 2003; Bensmaia & Hollins, 2005; Yau et al., 2009; Saal, Wang, & Bensmaia, 2016) that are reproduced faithfully by temporally precise spiking patterns (Mackevicius, Best, Saal, & Bensmaia, 2012; Weber et al., 2013). These two streams of information are then carried by tactile nerve fibers to the brain, where they are integrated and transformed through successive stages of neural processing to ultimately culminate in a tactile percept of texture.
What Is Texture?
Classically, the term “texture” refers to the feel or appearance of an object’s surface. And yet, not every aspect of a surface is considered texture—for example, buttons on a video-game controller are shapes rather than features. So what are the qualities that separate a shape from a texture? One distinction is that textural features are generally distributed across the extent of a surface, and their precise pattern is meaningless, while shape features tend to be more discrete and their configuration is typically meaningful. In touch, another distinction is the relevant spatial scale: A feature that is larger than the size of the fingerpad is not a textural one.
Over the last two decades, much progress has been made to quantitatively describe the stimulus parameters that define visual and auditory texture (Portilla & Simoncelli, 2000; McDermott, Schemitsch, & Simoncelli, 2013). These parameters can be described as statistical distributions that are consistent between different samples of a given texture, but vary between different kinds of texture. In other words, textures are defined by a set of statistics that characterize non-identical stimuli that are perceptually equivalent, known as metamers (Julesz, 1962, 1981). This framework has been quite fruitful for the visual system, where textures can be defined by their statistics (Portilla & Simoncelli, 2000), which can then be used to produce new images (metamers) that appear to have the same visual texture (Portilla & Simoncelli, 2000; Freeman, Ziemba, Heeger, Simoncelli, & Movshon, 2013; Ziemba, Freeman, Movshon, & Simoncelli, 2016; Ziemba, Freeman, Simoncelli, & Movshon, 2018). A similar approach has been fruitfully applied to generate auditory textures, such as the sound of a burbling stream or crackling fire (McDermott & Simoncelli, 2011; McDermott et al., 2013; McWalter, McDermott, McWalter, & McDermott, 2018).
This approach cannot straightforwardly be applied to tactile texture, however, because early processing—well established for vision and audition and crucial for the generation of metamers—has not been established for touch. This challenge stems in part from the biomechanical interactions between skin and surface, which complicate the relationship between stimulus, neural response, and percept. Furthermore, despite advances in 3D printing, to generate arbitrary tactile surfaces is uniquely difficult compared to creating visual or auditory textures. Not only must surfaces match on a micron-level of three-dimensional detail, but tactile objects also contain difficult-to-characterize material properties such as compliance and viscosity. Facsimiles of textural percepts have been created through the clever use of vibrating surfaces (Winfield, Glassmire, Colgate, & Peshkin, 2007; Bau, Poupyrev, Israr, & Harrison, 2010; Chubb, Colgate, & Peshkin, 2010), but no simulation approach is currently able to elicit a natural textural percept. Thus, little is known about the mapping between surface features and the tactile experience to which they give rise.
The Perceptual Space of Texture
When prompted, subjects will consistently describe different textures as rough or smooth, or hard and soft (Hollins et al., 1993). Quantitative ratings of these characteristics are consistent across individuals (Connor, Hsiao, Phillips, & Johnson, 1990; Friedman, Hester, Green, & LaMotte, 2008b) as are ratings of the dissimilarity of pairs of textures (Hollins et al., 2000a). In fact, these two sets of ratings are linked: Dissimilarity ratings of texture pairs consistently yield a perceptual space that is well described by a small number of dimensions, and these dimensions generally map onto nameable textural continua, including rough/smooth, hard/soft, sticky/slippery, and warm/cool (Figure 1) (Hollins et al., 1993, 2000a; Picard et al., 2003; Bergmann Tiest & Kappers, 2006; Okamoto et al., 2013).
The dominant and most studied perceptual dimension of texture is roughness (Lederman & Taylor, 1972; Hollins et al., 1993, 2000a). Perceived roughness is a consistent property of surface microstructure: human observers overwhelmingly agree on the relative roughness of textured surfaces (Stevens & Harris, 1962; Lederman, 1983; Sathian, Goodwin, John, & Darian-Smith, 1989; Connor et al., 1990; Connor & Johnson, 1992; Blake, Hsiao, & Johnson, 1997a). However, the relationship between the spatial geometry of surface features and roughness is not always straightforward. For example, while the roughness of periodic gratings increases with increases in groove width (Taylor & Lederman, 1975; Sathian et al., 1989) and the roughness of sandpaper increases as grit size increases (Harper & Stevens, 1964), the roughness of embossed dot patterns is a complex function of dot spacing (Connor et al., 1990; Connor & Johnson, 1992; Sutu, Meftah, & Chapman, 2013; Tymms, Zorin, & Gardner, 2017), dot width (Blake et al., 1997a), and dot height (Figure 2) (Sutu et al., 2013). In fact, unlike most other sensory continua, there is no established physical determinant of perceived roughness. One possible determinant of roughness is the magnitude of time-varying fluctuations in the surface friction (Smith, Chapman, Deslandes, Langlais, & Thibodeau, 2002), but even this quantity cannot account for the fact that surfaces can be judged along the roughness continuum in the absence of motion between skin and surface (Hollins & Risner, 2000). Roughness is only loosely associated with any one surface property but rather is defined by aspects of the response in the somatosensory nerves (see “Neural mechanisms of texture—Roughness”).
The second major axis of texture perception is hardness/softness (Klatzky, Lederman, & Reed, 1989; Hollins et al., 2000a), which closely tracks surface compliance (Figure 3) (Harper & Stevens, 1964; Yoshioka, Bensmaia, Craig, & Hsiao, 2007; Friedman et al., 2008b). When touching a surface, differences in surface compliance lead to different distributions of force across the surface of the finger, both during initial contact and static grip. These forces provide multiple cues—in their spatial distribution and temporal progression—which can be used to extract information about compliance. Indeed, we reliably perceive hardness during static grip, a mode that minimizes temporal cues (though these are still present at the onset of the grip) (Friedman et al., 2008b), but we can also perceive the hardness of a surface explored through a rigid probe, an ability that relies on temporal cues from vibrations transmitted through the probe (LaMotte, 2000). When tactile cues are eliminated altogether through digital anesthesia, we can still under certain circumstances perceive hardness using only kinesthetic cues, signaling the movement of the fingers into the object (Srinivasan & LaMotte, 1995). Thus, the perception of hardness relies on the ability to integrate multiple streams of somatosensory information to reconstruct the physical compliance of a surface.
The third axis of texture is stickiness, which tracks the friction between skin and surface (Smith & Scott, 1996; Yoshioka et al., 2007). For natural textures, perceptual judgments of stickiness are often correlated with judgments of roughness (Hollins et al., 2000a), but this relationship can be broken if friction is controlled (Taylor & Lederman, 1975). While stickiness is a far weaker determinant of the perceptual experience of texture than are roughness or hardness (Hollins et al., 2000a), the ability to sense friction contributes to texture discrimination (Gueorguiev, Bochereau, Mouraux, Hayward, & Thonnard, 2016) and is critical to the determination of the force required to grasp an object (Cadoret & Smith, 1996; Augurelle, Smith, Lejeune, & Thonnard, 2003).
A fourth, modest axis of texture is warmth (Hollins et al., 2000a), associated with the thermal conductivity of the surface material. Indeed, at room temperature, objects are colder than is the body, so heat will tend to flow out of the skin and into the object. The rate of this heat transfer depends on the thermal conductivity of the material and determines the warmth of the surface, with higher heat transfer leading to cooler surfaces (Ho & Jones, 2006). In addition to being used to judge the material properties of surfaces, thermal conductivity is also associated with the tactile perception of surface wetness (Filingeri, Redortier, Hodder, & Havenith, 2013, 2015).
Perceptual Invariance of Texture
Remarkably, the perception of texture is stable across broad changes in the way textures are explored. While everyday surfaces are generally explored through active movements of the hand, textures that are passively presented to the skin are perceived to be similar to their actively explored counterparts (Lederman, 1981; Lamb, 1983; Verrillo, Bolanowski, & McGlone, 1999; Friedman et al., 2008b; Yoshioka et al., 2011). This perception is robust to changes in scanning speed (Lederman, 1974, 1983; Yoshioka et al., 2011; Boundy-Singer, Saal, & Bensmaia, 2017) and force (Lederman & Taylor, 1972; Lederman, 1981), which is surprising given the strong dependence of skin responses on these exploratory parameters (Delhaye, Hayward, Lefèvre, & Thonnard, 2012; Manfredi et al., 2014). In this sense, the construction of textural percepts draws a strong analogy with the context-invariant perception of objects in the visual (DiCarlo, Zoccolan, & Rust, 2012) and auditory (Marozeau, de Cheveigné, McAdams, & Winsberg, 2003) systems.
Skin Response during Texture Exploration
Contact between the skin and a textured surface results in a spatial pattern of loads (or forces) on the skin’s surface (Taylor & Lederman, 1975; Dandekar, Raju, & Srinivasan, 2003; Sripati, Bensmaia, et al., 2006; Kim, Sripati, & Bensmaia, 2010; Saal, Delhaye, et al., 2017). These loads directly reflect the spatial layout of the surface percept. Importantly, these forces are not a simple recapitulation of the surface structure: Loads are greater at edges and corners and weaker or nil for small internal features. These forces then propagate through the skin, producing patterns of stresses and strains at the location of the mechanoreceptors, which transduce these skin deformations and convert them into neural signals. Skin mechanics has two important consequences on the perception of surface features. First, it distorts them, amplifying certain features (corners, edges) and obscuring others (small internal ones). Second, as these forces propagate deeper into the skin, their spatial patterning becomes increasingly blurred, which causes further masking of fine spatial features. Thus, while these spatial patterns of deformation account for some aspects of texture perception (Taylor & Lederman, 1975), they do not account for the perception of fine surface features because these are filtered out. Indeed, while coarse surface features (>1 mm) can be perceived by pressing the surface against the fingertip—thereby producing these spatially patterned skin deformations—finer features cannot (Van Boven & Johnson, 1994; Sathian & Zangaladze, 1996; Hollins & Risner, 2000).
The perception of fine textural features requires movement between the surface and the skin (Katz, 1925; Hollins & Risner, 2000). Unlike static touch, active exploration of a texture drives vibrations in the skin (Scheibert, Leurent, Prevost, & Debregeas, 2009), and the structure of these vibrations depends critically on surface microgeometry (Figure 4) (Bensmaia & Hollins, 2003; Bensmaia & Hollins, 2005; Delhaye et al., 2012; Manfredi et al., 2014). Furthermore, these vibrations are perceptually relevant: Differences in the texture-driven vibrations predict how dissimilar textures feel (Bensmaia & Hollins, 2005), vibrations imposed onto textures make textures feel rougher (Hollins, Fox, & Bishop, 2000b), and adaption of vibration-sensitive nerve fibers impairs subjects’ ability to discriminate fine but not coarse textures (Lederman, Loomis, & Williams, 1982; Hollins, Bensmaia, & Washburn, 2001). These results form the basis of the duplex theory of tactile texture perception (Katz, 1925; Hollins & Risner, 2000): The perception of coarse features relies on spatial patterns of skin deformation, and the perception of fine features relies on skin vibrations elicited during texture scanning.
Neural Mechanisms of Texture
Primer on the Neural Basis of Touch
Fine discriminative touch with the palmar surface of the hand relies on three main classes of tactile fibers (Abraira & Ginty, 2013): slowly adapting type-1 (SA1) fibers, which innervate Merkel cells, rapidly adapting (RA) fibers, which innervate Meissner corpuscles, and PC fibers, which terminate in Pacinian corpuscles (Figure 5, Table 1). A fourth type of nerve fiber, slowly adapting type-2 fibers (SA2), innervates Ruffini end-organs, a mechanoreceptor that only sparsely innervates the glabrous skin of humans and is absent in non-human primates (Paré, Smith, & Rice, 2002; Paré, Behets, & Cornu, 2003) so less is known about their responses to texture.
Table 1. Cutaneous Mechanoreceptors. Typical response properties of the three main mechanoreceptors in the glabrous skin. While different afferent types respond differently to skin deformations, they are typically all activated during every day interactions with objects.
Slowly adapting type 1 (SA1)
Rapidly adapting (RA)
Pacinian corpuscle-associated (PC)
Signals from these three populations of fibers carried by the somatosensory nerves through the spinal cord and synapse (ipsilaterally) onto neurons in the cuneate nucleus, in the medulla oblongata of the brainstem. Neurons from this nucleus send axons across the midline to the contralateral ventral posterolateral nucleus of the thalamus (VPL). The few studies of tactile responses within these two nuclei suggest that their patterns of activity look qualitatively similar to those of peripheral afferents (Douglas, Ferrington, & Rowe, 1978; Ghosh, Turman, Vickery, & Rowe, 1992; Zhang et al., 2001), but texture representations have not been systematically investigated there.
Neurons in VPL primarily project to anterior parietal cortex (APC) (Jones, 1975, 1983; Jones & Burton, 1976; Jones & Friedman, 1982; Padberg et al., 2009)—located on the posterior bank of the central sulcus and on the postcentral gyrus—which comprises four cortical modules, namely Brodmann’s areas 3a, 3b, 1, and 2, progressing posteriorly (Geyer, Schleicher, & Zilles, 1999). Although all cortical fields in APC receive direct projections from thalamus, cutaneous neurons in thalamus project primarily to areas 3b, 1, and 2, while proprioceptive ones project to areas 3a and 2 (Friedman & Jones, 1981). Only area 3b receives thalamocortical input that is characteristic of primary sensory areas, and so this area is considered to be primary somatosensory cortex proper (Kaas, 1983).
From APC, somatosensory signals diverge along two parallel streams, dorsal and ventral (Gardner, 2010; Sathian, 2016). Little is known about the elaboration of texture signals in the dorsal stream, which includes posterior parietal cortex (Brodmann’s areas 5 and 7), an area generally associated with visuo-motor transformations (Andersen & Buneo, 2002; Gardner, 2010; Gharbawie, Stepniewska, Qi, & Kaas, 2011). Rather, the conscious experience of tactile texture is thought to rely on propagation of texture signals along the ventral stream (Ledberg, O’Sullivan, Kinomura, & Roland, 1995; Roland, O’Sullivan, & Kawashima, 1998; Kitada et al., 2005; Stilla & Sathian, 2008; Sathian et al., 2011; Simões-Franklin, Whitaker, & Newell, 2011; Kaas, van Mier, Visser, & Goebel, 2013; Sathian, 2016). This stream includes the lateral parietal cortex (LPC), consisting of areas PV and S2, and is known as the parietal operculum in humans (Krubitzer, Clarey, Tweedale, Elston, & Calford, 1995; Sathian, 2016). Because the LPC contains projections to regions of insular cortex that eventually connect to the amygdala and hippocampus (Friedman et al., 1986), the ventral pathway is thought to underlie tactile object recognition, perception, and memory.
The perception of textural features on the coarse end of the tangible spectrum (~1 mm or greater) is mediated by the spatial pattern of activation across tactile fibers innervating the skin. Only two populations of fibers have the necessary spatial resolution to carry this information: (1) SA1 fibers, characterized by small receptive fields (2–3 mm diameter on the macaque fingertip, [Vega-Bermudez & Johnson, 1999]) and dense innervation the skin, with as many as 1.4/mm2 in the fingertip (Johansson & Vallbo, 1979; Darian-Smith & Kenins, 1980), and (2) RA fibers, characterized by slightly larger receptive fields (3–5 mm diameter on the macaque fingertip, [Vega-Bermudez & Johnson, 1999]) and slightly denser innervation in the dermal papillae (1.7/mm2 on the fingertips than SA1 fibers [Johansson & Vallbo, 1979; Darian-Smith & Kenins, 1980]). Of these two classes of nerve fibers, SA1 afferents most faithfully carry the shape of surface features. SA1 fibers persistently fire in response to statically indented tactile shape, and their response is more spatially selective than that of RA or PC afferents (Figure 6) (Phillips & Johnson, 1981; Goodwin, Browning, & Wheat, 1995; Goodwin, Macefield, & Bisley, 1997; Wheat, Goodwin, & Browning, 1995; Bisley, Goodwin, & Wheat, 2000). Individual SA2 afferents also exhibit shape-selective responses (Jenmalm, Birznieks, Goodwin, & Johansson, 2003), but the SA2 population lacks the dense innervation of SA1 afferents (Johansson, 1978). During active touch, all populations of SA1, RA, and PC afferents are all robustly activated, but the spatial image relayed by SA1 afferents is sharper than that of its RA counterpart (Figure 7) (Johnson & Lamb, 1981; Phillips, Johnson, & Hsiao, 1988; Connor et al., 1990; LaMotte, Lu, & Srivasan, 1996; Blake, Johnson, & Hsiao, 1997b). Thus, SA1 fibers encode spatial patterns in a manner analogous to photoreceptors in the retina and their spatial resolution (around 0.5–1 mm, [Phillips & Johnson, 1981]) is thought to mediate performance on standard tests of tactile acuity (Loomis, 1980; Johnson & Phillips, 1981).
In anterior parietal cortex, neurons exhibit strong selectivity for spatial patterns impinging upon the skin. Specifically, the receptive fields of neurons in area 3b consist of excitatory and inhibitory subfields (Figure 8) (DiCarlo, Johnson, & Hsiao, 1998; Sripati, Yoshioka, Denchev, Hsiao, & Johnson, 2006; Lieber & Bensmaia, 2018) in different configurations, which confers to each neuron a preference for a specific spatial feature. This receptive structure is highly analogous to that of neurons in primary visual cortex and can be approximated by a Gabor function (Bensmaia et al., 2008). Importantly, the implied spatial differentiation computation that these neurons implement is precisely that predicted from studies of the peripheral representation of embossed dot patterns (Connor et al., 1990; Connor & Johnson, 1992) (see “Neural mechanisms of texture—Roughness”), providing converging evidence of the role of spatial computations in texture processing. In fact, individual neurons in APC respond robustly to textured surfaces scanned across their receptive fields, and show graded responses to textures with varying coarse spatial structure (e.g., gratings or dot patterns that vary in spatial period) (Darian-Smith et al., 1982; Sinclair & Burton, 1991; Burton & Sinclair, 1994; Tremblay et al., 1996). While individual neurons in APC tend to receive convergent input from multiple classes of tactile fibers (Pei et al., 2009a; Saal, Harvey, & Bensmaia, 2015; Lieber & Bensmaia, 2018), neurons that best differentiate coarse textural features tend to receive strong input from SA1 fibers (Figure 9) (Lieber & Bensmaia, 2018).
While the spatial image carried by SA1 fibers is effective for relaying information about coarse textural features, it lacks the resolution to encode finer features (smaller than ~1 mm), due to limits set by the mechanical filtering by the skin and the innervation density of tactile nerve fibers (Figure 10) (Phillips & Johnson, 1981; Sripati, Bensmaia, et al., 2006; Weber et al., 2013) (see “Skin response during texture exploration”). In fact, fine features can be discerned only during dynamic contact, when the relative motion between the finger and surface drives texture-specific skin vibrations (Bensmaia & Hollins, 2003; Bensmaia & Hollins, 2005; Delhaye et al., 2012; Manfredi et al., 2014). These characteristic skin vibrations cannot be encoded by SA1 fibers, as these afferents do not respond to skin vibrations in the relevant frequency range (>50 Hz, e.g., for small features, <1 mm, even moving at a relatively slow speed, 50 mm/s) (Talbot et al., 1968; Bensmaia et al., 2005; Mackevicius et al., 2012; Callier et al., 2015). Rather, these vibrations drive precise, repeatable temporal spiking patterns in RA and PC afferents that are highly texture-specific and thus informative about the fine features of a surface (Figure 11) (Weber et al., 2013).
In anterior parietal cortex, the amplitude and fine timing of these afferent spiking patterns are reflected in the responses of their downstream recipients (Mountcastle et al., 1969; Salinas et al., 2000; Harvey et al., 2013). Vibratory amplitude is encoded in firing rates across the frequency range. Vibratory frequency is encoded in both temporal patterning and firing rates at low vibratory frequencies (<50 Hz) but only in temporal patterning (and not in firing rates) at high vibratory frequencies (>50 Hz). Indeed, at these high vibratory frequencies, firing rates are dependent on amplitude but not frequency. The net result is that precisely timed spiking patterns in a subpopulation of APC neurons convey texture information (Figure 12) (Lieber & Bensmaia, 2018). These neurons, which tend to receive strong input from PC fibers and exhibit phase-locked spiking when periodic textures are scanned across their receptive fields. While this timing signal could, in principle, contribute to the processing and perception of fine textural features, this texture information is redundantly carried in firing rates, so the role of temporal patterning in texture signaling in cortex remains to be demonstrated. Neurons that exhibit a sensitivity to fine surface features tend to be found within area 1, where functional and anatomical evidence has suggested a preponderance of neurons with strong PC input (Paul et al., 1972; Hyvärinen & Poranen, 1978; Merzenich et al., 1978; Hyvärinen et al., 1980; Padberg et al., 2009; Lieber & Bensmaia, 2018). Notably, lesions to area 1 seem to lead to specific deficits in texture perception (Randolph & Semmes, 1974; Carlson, 1981) though this area does not seem to carry a more elaborate representation of texture across the tangible range than do its neighbors (Lieber & Bensmaia, 2018).
Integration of spatial and temporal codes
These two encoding mechanisms for texture—spatial and temporal—provide a mechanistic underpinning for the duplex theory of tactile texture perception (Katz, 1925; Hollins & Risner, 2000): coarse features are encoded by the spatial pattern of activity across SA1 (and perhaps RA) fibers, fine features are encoded by temporally precise patterns of activity within RA and PC fibers. As most textures comprise both coarse and fine features, these two streams of information must eventually be combined. Within APC, this process has already begun. Functional evidence suggests that signals from all three populations of tactile fibers (SA1, RA, and PC) converge onto individual cortical neurons, as early as area 3b (Hyvärinen & Poranen, 1978; Pei et al., 2009b; Saal & Bensmaia, 2014; Lieber & Bensmaia, 2018). Specifically, most neurons exhibit sustained responses to a skin indentation, a signature of SA1 input (Pei et al., 2009b), and nearly all neurons also exhibit strong offset responses, a signature of RA and/or PC input (Sur et al., 1984; Pei et al., 2009b). Furthermore, cortical responses to complex vibration responses can only be explained by the integration of RA and PC signals (Saal et al., 2015). As might be expected, then, the responses of most neurons in APC encode both coarse and fine features, implying an integration of the spatial and temporal codes for texture (Lieber & Bensmaia, 2018).
The neural code for roughness—the primary axis of texture—was first established by comparing judgments of roughness of embossed dot patterns, obtained from human observers, to the responses evoked by these textures in the three populations of tactile fibers. In an elegant series of studies, Johnson and colleagues tested a set of hypotheses as to the neural determinants for roughness and eliminated all but one (Connor et al., 1990; Connor & Johnson, 1992; Blake et al., 1997a): across all conditions tested, the variation (or degree of inhomogeneity) across the responses of SA1 fibers could account, with remarkable precision, for roughness judgments (Figure 13). That is, to the extent that all SA1 fibers respond equally to a surface—indicating a lack of asperities—a surface will be perceived as smooth; to the extent that asperities are distributed across the surface, they will excite some SA1 fibers and not others, and the surface will be perceived as rough (Goodman & Bensmaia, 2017). The computation implied by this neural code for roughness can be implemented by a spatial filter consisting of a positively and negatively weighted lobe offset by 2–4 mm (a Gabor filter) passed across the spatial pattern of activation in this population of fibers (Connor & Johnson, 1992; Lieber et al., 2017). The friction between surface and finger also contributes to its perceived roughness (Smith et al., 2002), but a coarse texture can be perceived as rough even in the absence of movement between skin and surface (Hollins & Risner, 2000), highlighting the fact that there is no single well defined physical determinant of perceived roughness.
That SA1 fibers carry a faithful neural image of embossed dot patterns that accounts for roughness judgments was taken as evidence that SA1 fibers mediate tactile perception of texture across the tangible range (Yoshioka et al., 2001a). However, the spatial image carried by SA1 fibers lacks the resolution to encode fine features, and thus cannot account for roughness perception of finely textured surfaces, including sandpapers (Lieber et al., 2017). Rather, the peripheral code for fine texture roughness relies on temporally structured patterns of activity within RA and PC afferents. In parallel to the spatial computation, a computation of temporal variation in RA and PC responses—the extent to which responses of individual fibers are inhomogeneous in time—contributes to perceived roughness. The computation implied by the temporal variation code can be represented by a temporal Gabor filter (of width 10–20 ms) passed across the responses of individual RA and PC fibers (Weber et al., 2013; Saal et al., 2015; Lieber et al., 2017). In summary then, tactile roughness likely depends on two parallel codes: a spatial variation code for coarse features and a temporal variation code for finer features.
In everyday tactile experience, most surfaces comprise both fine and coarse features. Thus, the central nervous system cannot selectively listen to either a spatial or temporal code on a texture by texture basis; rather, it must combine signals from both of these encoding mechanisms to achieve a unified textural percept. Neurophysiological results show that the roughness of natural textures is well explained by a neural code that combines signals from SA1, RA, and PC afferents ((Weber et al., 2013; Lieber et al., 2017), though an opponency role has been proposed for SA1 signals, [see Gescheider et al., 2005; Gescheider & Wright, 2013, 2018]). While SA1 afferents best explain the roughness of dot patterns and gratings (Blake et al., 1997a; Yoshioka et al., 2001b; Lieber et al., 2017), RA responses account for differences in roughness across everyday fabrics, and PC afferents account for the characteristic roughness of sandpapers (Figure 14) (Lieber et al., 2017). Therefore, the neural code for roughness is determined by the combined activity of all three classes of tactile fibers, and requires the integration of the spatial signals encoding coarse features and temporal signals encoding fine features.
In anterior parietal cortex, these divergent streams of spatial and temporal information are combined and transformed into a more explicit code for roughness. Because SA1, RA, and PC signals converge onto individual neurons within APC, these neurons can simultaneously account for the perception of both fine and coarse features. Furthermore, the responses of APC neurons are well described by Gabor-like filters for both spatial patterns (DiCarlo & Johnson, 2000; Bensmaia, Denchev, Dammann, Craig, & Hsiao, 2008) and temporal spiking sequences (Saal et al., 2015), just as predicted by studies investigating the neural code for roughness in the somatosensory nerves (Connor et al., 1990; Lieber et al., 2017). Because cortical responses reflect the variation computations that drive perceived roughness, cortical firing rates can account for human judgments of roughness (Burton & Sinclair, 1994; Chapman et al., 2002; Bourgeon et al., 2016; Lieber & Bensmaia, 2018).
Other perceptual continua of texture
While most work on texture coding has focused on roughness, the neural determinants of other textural continua have also been investigated. The consensus from psychophysical and neurophysiological experiments is that perceived hardness, like roughness, depends on both spatial and temporal codes. Surfaces of differing compliance lead to different spatiotemporal patterns of activation when they make contact with the skin. For example, at equal contact force, the area of contact between skin and surface is wider for soft than for hard surfaces and forces drop off more progressively for soft than hard surfaces. As a result, the spatial distribution of SA1 responses is shaped, in part, by surface compliance (Figure 15): SA1 fibers are activated over a wider area and the drop off in their activation is more progressive when contacting a compliant surface (Condon et al., 2014; Hudson et al., 2015). However, hardness can also be perceived through rapid tapping of surface with a probe (LaMotte, 2000), which elicits hardness-dependent vibrations in the probe which are transduced primarily by RA and PC fibers.
The neural underpinnings for other sensory continua of texture have not been investigated as systematically as have those for roughness and hardness. Stickiness is thought to be driven by tangential forces that stretch the skin during texture scanning, and both SA1 and RA fibers respond to tangential forces in the skin (as do SA2 fibers) (Birznieks et al., 2001, 2010). However, stickiness perception has not been experimentally linked to specific patterns of afferent activation. The perception of warmth/coolness—associated with the thermal conductivity of the surface material—is thought to be encoded by thermoreceptive fibers (Johnson et al., 1973, 1979; Darian-Smith et al., 1979b, 1979a; Ho & Jones, 2006), but it is unknown where and how these signals are integrated with other texture signals.
Texture perception is largely independent of exploratory parameters used to scan a surface, such as the scanning speed or contact force. This perceptual invariance stands in contrast to responses of peripheral afferents, which are strongly modulated by changes in scanning speed (Goodwin & Morley, 1987a; Phillips et al., 1992; DiCarlo & Johnson, 1999; Lieber et al., 2018) and, to a lesser extent, exploratory force (Goodwin & Morley, 1987b; Phillips et al., 1992; Saal, Suresh, et al., 2017). To achieve perceptual invariance, exploration-invariant representations of texture must be extracted from spatial and temporal patterns of peripheral activity. Intriguingly, neurons across APC show a range of responses that lie between these two extremes—some neurons exhibit texture responses that, like afferents, are strongly affected by changes in scanning speed, while others show texture responses that are almost entirely invariant to speed (Sinclair & Burton, 1991; DiCarlo & Johnson, 1999; Dépeault et al., 2013; Lieber et al., 2018). As a result, the population response to texture within APC can simultaneously carry information about texture and about exploratory parameters.
Neural correlates of perceptual invariance can be explained, in part, by existing encoding mechanisms. For example, the spatial encoding mechanism for coarse textural features is naturally invariant to changes in exploratory parameters. Unlike afferent firing rates, the spatial patterning of texture responses is robust to changes in scanning speed (Johnson & Lamb, 1981; Phillips et al., 1992), as is the spatial variation code for coarse texture roughness (Connor et al., 1990; Lieber et al., 2017). The somatosensory system may also leverage large-scale spatial patterning to explicitly encode information about exploratory parameters, and then use that information to correct texture signals for any systematic biases. For example, while populations of afferents with receptive fields over the area of contact with an object encode its shape, fibers with receptive fields outside the contact area encode contact force (Bisley et al., 2000).
In contrast to the spatial code, the temporal code that carries information about fine textural features is particularly sensitive to changes in scanning speed. Specifically, the structure of texture-driven spiking patterns in RA and PC afferents are dependent not only on the microstructure of the surface but also on the speed at which the skin moves across the surface (Weber et al., 2013; Manfredi et al., 2014). Specifically, texture-evoked patterns dilate or contract systematically with decreases or increases in scanning speed, respectively. Notably, texture-specific temporal patterning within APC shows this same dilation/contraction effect (Lieber et al., 2018). These predictable shifts in patterning mean that texture-specific information can be extracted from temporal patterns of activity, but only when scanning speed is taken into account and corrected for (Figure 16). Thus, for surfaces with finer features, the extraction of an invariant texture representation draws a parallel to the auditory phenomenon of timbre invariance across changes in fundamental frequency (Marozeau et al., 2003; Yau et al., 2009; Saal et al., 2016). In both cases, the ability to extract meaningful information from a temporally patterned signal relies on the predictable transformation of that signal’s harmonic stack along the frequency axis. How the auditory and somatosensory systems accomplish this task is not understood.
High-level representations of texture
The rich representation of texture within APC is further elaborated as it ascends the somatosensory neuraxis to lateral parietal cortex (LPC). Functional imaging studies have shown that LPC is strongly and selectively activated during texture related tasks (Ledberg et al., 1995; Roland et al., 1998; Kitada et al., 2005; Stilla & Sathian, 2008; Sathian et al., 2011; Simões-Franklin et al., 2011; Kaas et al., 2013; Sathian, 2016). At the single unit level, LPC responses differ from their APC counterparts in that LPC responses are alternately positively or negatively related to roughness whereas APC responses always increase with roughness (Figure 17A) (Sinclair & Burton, 1993; see also, a parallel result with vibrotactile stimuli, Salinas, Hernandez, Zainos, & Romo, 2000). This elaboration of the texture representation may be important for the extraction of higher-level features of texture, such as perceived hardness (Servos et al., 2001). LPC may also play a role in achieving a representation of texture that is invariant to changes in exploratory strategy: BOLD responses to texture in LPC are the same whether textures are actively scanned with the finger or passively presented by the experimenter (Simões-Franklin et al., 2011).
Unlike APC responses, which tend to encode a stimulus regardless of the task demands or behavioral context, LPC responses are highly task and context dependent (Jiang, Tremblay, & Chapman, 1997; Romo, Hernández, Zainos, Lemus, & Brody, 2002; Chapman & Meftah, 2005; Kitada et al., 2005; Meftah, Bourgeon, & Chapman, 2009). For example, when animals are trained to detect a change in surface texture, neurons within APC respond to the surface, independently of the task. By contrast, many neurons within LPC show “change-detection” response properties—that is, they signal a change in texture, regardless of the texture (Figure 17B) (Jiang et al., 1997). Functional imaging studies suggest that LPC may contain a persistent representation of tactile working memory in a texture task (Kaas et al., 2013; also see [de Lafuente & Romo, 2006]). LPC may also be a locus for more abstract representations of texture: functional imaging studies have shown that non-tactile inputs, such as spoken phrases suggestive of tactile texture, can drive activity within LPC (Lacey, Stilla, & Sathian, 2012).
Surfaces are ubiquitous and our sense of touch conveys exquisite information about their microstructure and material properties. Our perceptual experience of texture spans a wide range: surfaces can feel rough or smooth, hard or soft, velvety, fuzzy, etc. Texture percepts are consistent even as we move our hands over the surface in different ways. This rich and robust sense arises from different streams of neuronal activity: larger features of a surface are encoded in spatial patterns of activity in the nerve that mirror the large scale deformations they produce in the skin (on the order of millimeters), while finer features are encoded in temporal patterns of activity that reflect texture-specific skin vibrations. These two streams of information, spatial and temporal, are combined in cerebral cortex, where they give rise to a high dimensional representation of texture and thus to a complex perceptual space.
Abraira, V. E., & Ginty, D. D. (2013). The sensory neurons of touch. Neuron, 79, 618–639.Find this resource:
Andersen, R. A., & Buneo, C. A. (2002). Intentional maps in posterior parietal cortex. Annual Review of Neuroscience, 25, 189–220Find this resource:
Augurelle, A.-S., Smith, A. M., Lejeune, T., & Thonnard, J.-L. (2003). Importance of cutaneous feedback in maintaining a secure grip during manipulation of hand-held objects. Journal of Neurophysiology, 89(2), 665–671.Find this resource:
Bau, O., Poupyrev, I., Israr A., & Harrison, C. (2010). TeslaTouch: Electrovibration for touch surfaces. Proceedings of the 23rd annual ACM symposium on User interface software and technology (pp. 283–292). New York, NY: ACM.Find this resource:
Bensmaia, S. J., Denchev, P. V., Dammann, J. F., Craig, J. C., & Hsiao, S. S. (2008). The representation of stimulus orientation in the early stages of somatosensory processing. Journal of Neuroscience, 28, 776–786.Find this resource:
Bensmaia, S. J., & Hollins, M. (2003). The vibrations of texture. Somatosensory and Motor Research, 20, 33–43.Find this resource:
Bensmaia, S. J., & Hollins, M. (2005). Pacinian representations of fine surface texture. Perception and Psychophysics, 67, 842–854.Find this resource:
Bensmaia, S. J., Leung, Y. Y., Hsiao, S. S., & Johnson, K. O. (2005). Vibratory adaptation of cutaneous mechanoreceptive afferents. Journal of Neurophysiology, 94, 3023–3036.Find this resource:
Bergmann Tiest, W. M., & Kappers, A. M. L. (2006). Analysis of haptic perception of materials by multidimensional scaling and physical measurements of roughness and compressibility. Acta Psychologica (Amst), 121, 1–20.Find this resource:
Birznieks, I., Jenmalm, P., Goodwin, A. W., & Johansson, R. S. (2001). Encoding of direction of fingertip forces by human tactile afferents. Journal of Neuroscience, 21, 8222–8237.Find this resource:
Birznieks, I., Wheat, H. E., Redmond, S. J., Salo, L. M., Lovell, N. H., & Goodwin, A. W. (2010). Encoding of tangential torque in responses of tactile afferent fibres innervating the fingerpad of the monkey. The Journal of Physiology, 588, 1057–1072.Find this resource:
Bisley, J. W., Goodwin, A. W., & Wheat, H. E. (2000). Slowly adapting type I afferents from the sides and end of the finger respond to stimuli on the center of the fingerpad. Journal of Neurophysiology, 84, 57–64.Find this resource:
Blake, D. T., Hsiao, S. S., & Johnson, K. O. (1997a). Neural coding mechanisms in tactile pattern recognition: The relative contributions of slowly and rapidly adapting mechanoreceptors to perceived roughness. Journal of Neuroscience, 17, 7480–7489.Find this resource:
Blake, D. T., Johnson, K. O., & Hsiao, S. S. (1997b). Monkey cutaneous SAI and RA responses to raised and depressed scanned patterns: Effects of width, height, orientation, and a raised surround. Journal of Neurophysiology, 78, 2503–2517.Find this resource:
Boundy-Singer, Z. M., Saal, H. P., & Bensmaia, S. J. (2017). Speed invariance of tactile texture perception. Journal of Neurophysiology, 118, 2371–2377.Find this resource:
Bourgeon, S., Dépeault, A., Meftah, E.-M., & Chapman, C. E. (2016). Tactile texture signals in primate primary somatosensory cortex and their relation to subjective roughness intensity. Journal of Neurophysiology, 115, 1767–1785.Find this resource:
Burton, H., & Sinclair, R. J. (1994). Representations of tactile roughness in thalamus and somatosensory cortex. Canadian Journal of Physiology and Pharmacology, 72, 546–557.Find this resource:
Cadoret G., & Smith, A. M. (1996). Friction, not texture, dictates grip forces used during object manipulation. Journal of Neurophysiology, 75, 1963–1969.Find this resource:
Callier T., Saal, H. P., Davis-Berg, E. C., & Bensmaia, S. J. (2015). Kinematics of unconstrained tactile texture exploration. Journal of Neurophysiology, 113(7), 3013–3020.Find this resource:
Carlson, M. (1981). Characteristics of sensory deficits following lesions of Brodmann’s areas 1 and 2 in the postcentral gyrus of Macaca mulatta. Brain Research, 204, 424–430.Find this resource:
Chapman, C. E., & Meftah, E.-M. (2005). Independent controls of attentional influences in primary and secondary somatosensory cortex. Journal of Neurophysiology, 94, 4094–4107.Find this resource:
Chapman, C. E., Tremblay, F., Jiang, W., Belingard, L., & Meftah, E. M. (2002). Central neural mechanisms contributing to the perception of tactile roughness. Behavioural Brain Research, 135(1–2), 225–233.Find this resource:
Chubb, E. C., Colgate, J. E., & Peshkin, M. A. (2010). ShiverPaD: A glass haptic surface that produces shear force on a bare finger. IEEE Transactions on Haptics, 3, 189–198.Find this resource:
Condon, M., Birznieks, I., Hudson, K., Chelvanayagam, D. K., Mahns, D., Olausson, H., & Macefield, V. G. (2014). Differential sensitivity to surface compliance by tactile afferents in the human finger pad. Journal of Neurophysiology, 111, 1308–1317.Find this resource:
Connor, C. E., Hsiao, S. S., Phillips J. R., & Johnson, K. O. (1990). Tactile roughness: Neural codes that account for psychophysical magnitude estimates. Journal of Neuroscience, 10, 3823–3836.Find this resource:
Connor, C. E., & Johnson, K. O. (1992). Neural coding of tactile texture: Comparison of spatial and temporal mechanisms for roughness perception. Journal of Neuroscience, 12, 3414–3426.Find this resource:
Dandekar, K., Raju, B. I., & Srinivasan, M. A. (2003). 3-D finite-element models of human and monkey fingertips to investigate the mechanics of tactile sense. Journal of Biomechanical Engineering, 125, 682–691.Find this resource:
Darian-Smith, I., Johnson, K. O., LaMotte, C., Kenins, P., Shigenaga, Y., & Ming, V. C. (1979a). Coding of incremental changes in skin temperature by single warm fibers in the monkey. Journal of Neurophysiology, 42, 1316–1331.Find this resource:
Darian-Smith, I., Johnson, K. O., LaMotte, C., Shigenaga, Y., Kenins, P., & Champness, P. (1979b). Warm fibers innervating palmar and digital skin of the monkey: Responses to thermal stimuli. Journal of Neurophysiology, 42, 1297–1315.Find this resource:
Darian-Smith, I., & Kenins, P. (1980). Innervation density of mechanoreceptive fibres supplying glabrous skin of the monkey’s index finger. The Journal of Physiology, 309, 147–155.Find this resource:
Darian-Smith, I., Sugitani, M., Heywood, J., Karita K., & Goodwin, A. W. (1982). Touching textured surfaces: Cells in somatosensory cortex respond both to finger movement and to surface features. Science, 218, 906–909.Find this resource:
de Lafuente, V., & Romo, R. (2006). Neural correlate of subjective sensory experience gradually builds up across cortical areas. Proceedings of the National Academy of Sciences of the United States of America, 103, 14266–14271.Find this resource:
Delhaye, B., Hayward, V., Lefèvre, P., & Thonnard, J.-L. (2012). Texture-induced vibrations in the forearm during tactile exploration. Frontiers in Behavioral Neuroscience, 6, 37.Find this resource:
Dépeault, A., Meftah, E.-M., & Chapman, C. E. (2013). Neuronal correlates of tactile speed in primary somatosensory cortex. Journal of Neurophysiology, 110, 1554–1566.Find this resource:
DiCarlo J. J., & Johnson, K. O. (1999). Velocity invariance of receptive field structure in somatosensory cortical area 3b of the alert monkey. Journal of Neuroscience, 19, 401–419.Find this resource:
DiCarlo, J. J., & Johnson, K. O. (2000). Spatial and temporal structure of receptive fields in primate somatosensory area 3b: Effects of stimulus scanning direction and orientation. Journal of Neuroscience, 20, 495–510.Find this resource:
DiCarlo, J. J., Johnson, K. O., & Hsiao, S. S. (1998). Structure of receptive fields in area 3b of primary somatosensory cortex in the alert monkey. Journal of Neuroscience, 18, 2626–2645.Find this resource:
DiCarlo, J. J., Zoccolan, D., & Rust, N. C. (2012). How does the brain solve visual object recognition? Neuron, 73, 415–434.Find this resource:
Douglas, P. R., Ferrington, D. G., & Rowe, M. (1978). Coding of information about tactile stimuli by neurones of the cuneate nucleus. The Journal of Physiology, 285, 493–513.Find this resource:
Filingeri, D., Redortier, B., Hodder, S., & Havenith, G. (2013). The role of decreasing contact temperatures and skin cooling in the perception of skin wetness. Neuroscience Letters, 551, 65–69.Find this resource:
Filingeri, D., Redortier, B., Hodder, S., & Havenith, G. (2015). Warm temperature stimulus suppresses the perception of skin wetness during initial contact with a wet surface. Skin Research and Technology, 21, 9–14.Find this resource:
Freeman, J., Ziemba, C. M., Heeger, D. J., Simoncelli, E. P., & Movshon, J. A. (2013). A functional and perceptual signature of the second visual area in primates. Nature Neuroscience, 16(7), 974–981.Find this resource:
Friedman D., & Jones, E. G. (1981). Thalamic input to areas 3a and 2 in monkeys. Journal of Neurophysiology, 45, 59–85.Find this resource:
Friedman, D. P., Murray, E. A., O’Neill, J. B., & Mishkin, M. (1986). Cortical connections of the somatosensory fields of the lateral sulcus of macaques: Evidence for a corticolimbic pathway for touch. The Journal of Comparative Neurology, 252(3), 323–347.Find this resource:
Friedman, R. M., Chen, L. M., & Roe, A. W. (2008a). Responses of areas 3b and 1 in anesthetized squirrel monkeys to single- and dual-site stimulation of the digits. Journal of Neurophysiology, 100, 3185–3196.Find this resource:
Friedman, R. M., Hester, K. D., Green, B. G., & LaMotte, R. H. (2008b). Magnitude estimation of softness. Experimental Brain Research, 191, 133–142.Find this resource:
Gardner, E. P. (2010). Dorsal and ventral streams in the sense of touch. In Richard H. Masland, Thomas D. Albright, Thomas D. Albright, Richard H. Masland, Peter Dallos, Donata Oertel, . . . Esther P. Gardner (Eds.), The senses: A comprehensive reference (pp. 233–258). Cambridge, MA: Elsevier Press.Find this resource:
Gescheider, G. A., Bolanowski, S. J., Greenfield, T. C., & Brunette, K. E. (2005). Perception of the tactile texture of raised-dot patterns: A multidimensional analysis. Somatosensory and Motor Research, 22(3), 127–140.Find this resource:
Gescheider, G. A., & Wright, J. H. (2013). Roughness perception in tactile channels: Evidence for an opponent process in the sense of touch. Somatosensory and Motor Research, 30, 120–132.Find this resource:
Gescheider, G. A., & Wright, J. H. (2018). Perception of the tactile texture of raised-dot patterns: Further evidence of an opponent process in the sense of touch opponent process in the sense of touch. Somatosensory and Motor Research, 35(2), 59–68.Find this resource:
Geyer, S., Schleicher, A., & Zilles, K. (1999). Areas 3a, 3b, and 1 of human primary somatosensory cortex: 1. Microstructural organization and interindividual variability. Neuroimage, 10, 63–83.Find this resource:
Gharbawie, O. A., Stepniewska, I., Qi, H., & Kaas, J. H. (2011). Multiple parietal-frontal pathways mediate grasping in macaque monkeys. Journal of Neuroscience, 31, 11660–11677.Find this resource:
Ghosh, S., Turman, A. B., Vickery, R. M., & Rowe, M. J. (1992). Responses of cat ventroposterolateral thalamic neurons to vibrotactile stimulation of forelimb footpads. Experimental Brain Research, 92, 286–298.Find this resource:
Goodwin, A. W., Browning, A. S., & Wheat, H. E. (1995). Representation of curved surfaces in responses of mechanoreceptive afferent fibers innervating the monkey’s fingerpad. Journal of Neuroscience, 15, 798–810.Find this resource:
Goodwin, A. W., Macefield, V. G., & Bisley, J. W. (1997). Encoding of object curvature by tactile afferents from human fingers. Journal of Neurophysiology, 78, 2881–2888.Find this resource:
Goodwin, A. W., & Morley, J. W. (1987a). Sinusoidal movement of a grating across the monkey’s fingerpad: Representation of grating and movement features in afferent fiber responses. Journal of Neuroscience, 7, 2168–2180.Find this resource:
Goodwin, A. W., & Morley, J. W. (1987b). Sinusoidal movement of a grating across the monkey’s fingerpad: Effect of contact angle and force of the grating on afferent fiber responses. Journal of Neuroscience, 7, 2192–2202.Find this resource:
Goodman, J. M., & Bensmaia, S. J. (2017). A variation code accounts for the perceived roughness of coarsely textured surfaces. Scientific Reports, 7.Find this resource:
Gueorguiev, D., Bochereau, S., Mouraux, A., Hayward, V., & Thonnard, J. L. (2016). Touch uses frictional cues to discriminate flat materials. Scientific Reports, 6.Find this resource:
Guest, S., Dessirier, J. M., Mehrabyan, A., McGlone, F., Essick, G., Gescheider, G., Fontana, A., Xiong, R., Ackerley, R., & Blot, K. (2011). The development and validation of sensory and emotional scales of touch perception. Attention, Perception, Psychophysics, 73, 531–550.Find this resource:
Harper, R., & Stevens, S. S. (1964). Subjective hardness of compliant materials. The Quarterly Journal of Experimental Psychology, 16, 204–215.Find this resource:
Harvey, M. A., Saal, H. P., Dammann, J. F., & Bensmaia, S. J. (2013). Multiplexing stimulus information through rate and temporal codes in primate somatosensory cortex. PLOS Biology, 11.Find this resource:
Ho, H.-N., & Jones, L. A. (2006). Contribution of thermal cues to material discrimination and localization. Perception and Psychophysics, 68, 118–128.Find this resource:
Hollins, M., Bensmaia, S., Karlof, K., & Young, F. (2000a). Individual differences in perceptual space for tactile textures: Evidence from multidimensional scaling. Perception and Psychophysics, 62, 1534–1544.Find this resource:
Hollins, M., Bensmaia, S. J., & Washburn, S. (2001). Vibrotactile adaptation impairs discrimination of fine, but not coarse, textures. Somatosensory and Motor Research, 18, 253–262.Find this resource:
Hollins, M., Faldowski, R., Rao, S., & Young, F. (1993). Perceptual dimensions of tactile surface texture: A multidimensional scaling analysis. Perception and Psychophysics, 54, 697–705.Find this resource:
Hollins, M., Fox A., & Bishop, C. (2000b). Imposed vibration influences perceived tactile smoothness. Perception, 29, 1455–1465.Find this resource:
Hollins, M., & Risner, S. R. (2000). Evidence for the duplex theory of tactile texture perception. Perception and Psychophysics, 62, 695–705.Find this resource:
Hudson, K. M., Condon, M., Ackerley, R., McGlone, F., Olausson, H., Macefield, V. G., & Birznieks, I. (2015). Effects of changing skin mechanics on the differential sensitivity to surface compliance by tactile afferents in the human finger pad. Journal of Neurophysiology, 114(4), 2249–2257.Find this resource:
Hyvärinen, J., & Poranen, A. (1978). Receptive field integration and submodality convergence in the hand area of the post-central gyrus of the alert monkey. The Journal of Physiology, 283, 539–556.Find this resource:
Hyvärinen, J., Poranen, A., & Jokinen, Y. (1980). Influence of attentive behavior on neuronal responses to vibration in primary somatosensory cortex of the monkey. Journal of Neurophysiology, 43, 870–882.Find this resource:
Jenmalm, P., Birznieks, I., Goodwin, A. W., & Johansson, R. S. (2003). Influence of object shape on responses of human tactile afferents under conditions characteristic of manipulation. European Journal of Neuroscience, 18(1), 164–176.Find this resource:
Jiang, W., Tremblay, F., & Chapman, C. E. (1997). Neuronal encoding of texture changes in the primary and the secondary somatosensory cortical areas of monkeys during passive texture discrimination. Journal of Neurophysiology, 77, 1656–1662.Find this resource:
Johansson, R. (1978). Tactile sensibility in the human hand: Receptive field characteristics of mechanoreceptive units in the glabrous skin area. The Journal of Physiology, 101–123.Find this resource:
Johansson, R., & Vallbo, Å. (1979). Tactile sensibility in the human hand: Relative and absolute densities of four types of mechanoreceptive units in glabrous skin. The Journal of Physiology, 286(1), 283–300.Find this resource:
Johansson, R. S., & Vallbo Å. B. (1983). Tactile sensory coding in the glabrous skin of the human hand. Trends in Neurosciences, 6, 27–32.Find this resource:
Johnson, K., & Lamb, G. (1981). Neural mechanisms of spatial tactile discrimination: Neural patterns evoked by braille-like dot patterns in the monkey. The Journal of Physiology, 310(1), 117–144.Find this resource:
Johnson, K. O. (2001). The roles and functions of cutaneous mechanoreceptors. Current Opinion in Neurobiology, 11, 455–461.Find this resource:
Johnson, K. O., Darian-Smith, I., & LaMotte, C. (1973). Peripheral neural determinants of temperature discrimination in man: A correlative study of responses to cooling skin. Journal of Neurophysiology, 36, 347–370.Find this resource:
Johnson, K. O., Darian-Smith, I., LaMotte, C., Johnson, B., & Oldfield, S. (1979). Coding of incremental changes in skin temperature by a population of warm fibers in the monkey: Correlation with intensity discrimination in man. Journal of Neurophysiology, 42, 1332–1353.Find this resource:
Johnson, K. O., & Phillips, J. R. (1981). Tactile spatial resolution. I. Two-point discrimination, gap detection, grating resolution, and letter recognition. Journal of Neurophysiology, 46(6), 1177–1192.Find this resource:
Jones, E. G. (1975). Lamination and differential distribution of thalamic afferents within the sensory-motor cortex of the squirrel monkey. The Journal of Comparative Neurology, 160, 167–203.Find this resource:
Jones, E. G. (1983). Lack of collateral thalamocortical projections to fields of the first somatic sensory cortex in monkeys. Experimental Brain Research, 52, 375–384.Find this resource:
Jones, E. G., & Burton, H. (1976). Areal differences in the laminar distribution of thalamic afferents in cortical fields of the insular, parietal and temporal regions of primates. The Journal of Comparative Neurology, 168, 197–247.Find this resource:
Jones, E. G., & Friedman, D. P. (1982). Projection pattern of functional components of thalamic ventrobasal complex on monkey somatosensory cortex. Journal of Neurophysiology, 48, 521–544.Find this resource:
Julesz, B. (1962). Visual pattern discrimination. IRE Transactions on Information Theory, 8, 84–92.Find this resource:
Julesz, B. (1981). Textons, the elements of texture perception, and their interactions. Nature, 290(5802), 91.Find this resource:
Kaas A. L., van Mier, H., Visser, M., & Goebel, R. (2013). The neural substrate for working memory of tactile surface texture. Human Brain Mapping, 34, 1148–1162.Find this resource:
Kaas, J. H. (1983). What, if anything, is SI? Organization of first somatosensory area of cortex. Physiol Rev, 63, 206–231.Find this resource:
Katz, D. (1925). The world of touch. Edited by L. E. Krueger. Hillsdale, NJ: Erlbaum.Find this resource:
Kim, S. S., Sripati, A. P., & Bensmaia, S. J. (2010). Predicting the timing of spikes evoked by tactile stimulation of the hand. Journal of Neurophysiology, 104, 1484–1496.Find this resource:
Kitada, R., Hashimoto, T., Kochiyama, T., Kito, T., Okada, T., Matsumura, M., . . . & Sadato, N. (2005). Tactile estimation of the roughness of gratings yields a graded response in the human brain: An fMRI study. Neuroimage, 25, 90–100.Find this resource:
Klatzky, R. L., Lederman, S. J., & Metzger V. A. (1985). Identifying objects by touch: An “expert system.” Perception and Psychophysics, 37, 299–302.Find this resource:
Klatzky, R. L., Lederman, S. J., & Reed, C. (1989). Haptic integration of object properties: Texture, hardness, and planar contour. Journal of Experimental Psychology: Human Perception, 15, 45–57.Find this resource:
Krubitzer, L., Clarey, J., Tweedale, R., Elston, G., & Calford, M. (1995). A redefinition of somatosensory areas in the lateral sulcus of macaque monkeys. Journal of Neuroscience, 15, 3821–3839.Find this resource:
Lacey, S., Stilla, R., & Sathian, K. (2012). Metaphorically feeling: Comprehending textural metaphors activates somatosensory cortex. Brain Language, 120, 416–421.Find this resource:
Lamb, G. D. (1983). Tactile discrimination of textured surfaces: Psychophysical performance measurements in humans. The Journal of Physiology, 338, 551–565.Find this resource:
LaMotte, R. H. (2000). Softness discrimination with a tool. Journal of Neurophysiology, 83, 1777–1786.Find this resource:
LaMotte, R. H., Lu, C., & Srivasan, M. A. (1996). Tactile neutral codes for the shapes and orientation of objects. In Somesthesis and the Neurobiology of the Somatosensory Cortex (pp. 113–122). Basel, Switzerland, Birkhäuser Basel.Find this resource:
Ledberg, A., O’Sullivan, B. T., Kinomura, S., & Roland, P. E. (1995). Somatosensory activations of the parietal operculum of man: A PET study. European Journal of Neuroscience, 7, 1934–1941.Find this resource:
Lederman, S. J. (1974). Tactile roughness of grooved surfaces: The touching process and effects of macro-and microsurface structure. Perception and Psychophysics, 16, 385–395.Find this resource:
Lederman, S. J. (1981). The perception of surface roughness by active and passive touch. Bulletin of the Psychonomic Society, 18, 253–255.Find this resource:
Lederman, S. J. (1983). Tactual roughness perception: Spatial and temporal determinants. Canadian Journal of Psychology, 37, 498–511.Find this resource:
Lederman, S. J., Loomis, J. M., & Williams, D. A. (1982). The role of vibration in the tactual perception of roughness. Perception and Psychophysics, 32, 109–116.Find this resource:
Lederman, S. J., & Taylor, M. M. (1972). Fingertip force, surface geometry, and the perception of roughness by active touch. Perception and Psychophysics, 12, 401–408.Find this resource:
Lieber, J. D., & Bensmaia, S. J. (2019). High-dimensional representation of texture in somatosensory cortex of primates. Proceedings of the National Academy of Sciences, 116(8), 3268–3277.Find this resource:
Lieber, J. D., Long, K. H., & Bensmaia, S. J. (2018). Speed invariant coding of texture in somatosensory cortex. In The Neural Basis of Tactile Texture Perception (Doctoral dissertation). The University of Chicago.Find this resource:
Lieber, J. D., Xia, X., Weber, A. I., & Bensmaia, S. J. (2017). The neural code for tactile roughness in the somatosensory nerves. Journal of Neurophysiology, 118, 3107–3117.Find this resource:
Loomis, J. M. (1980). An investigation of tactile hyperacuity. Sensory processes, 3(4), 289–302.Find this resource:
Mackevicius, E. L., Best, M. D., Saal, H. P., & Bensmaia, S. J. (2012). Millisecond precision spike timing shapes tactile perception. Journal of Neuroscience, 32, 15309–15317.Find this resource:
Manfredi, L. R., Saal, H. P., Brown, K. J., Zielinski M. C., Dammann, J. F., Polashock, V. S., & Bensmaia, S. J. (2014). Natural scenes in tactile texture. Journal of Neurophysiology, 111, 1792–1802.Find this resource:
Marozeau, J., de Cheveigné, A., McAdams, S., & Winsberg, S. (2003). The dependency of timbre on fundamental frequency. Journal of the Acoustical Society of America, 114, 2946–2957.Find this resource:
McDermott, J. H., Schemitsch, M., & Simoncelli, E. P. (2013). Summary statistics in auditory perception. Nature Neuroscience, 16, 493–498.Find this resource:
McDermott, J. H., & Simoncelli, E. P. (2011). Sound texture perception via statistics of the auditory periphery: Evidence from sound synthesis. Neuron, 71, 926–940.Find this resource:
McWalter, R., McDermott, J. H., McWalter, R., & McDermott, J. H. (2018). Adaptive and Selective Time Averaging of Auditory Scenes. Current Biology, 28, 1–14.Find this resource:
Meftah, E.-M., Bourgeon, S., & Chapman, C. E. (2009). Instructed delay discharge in primary and secondary somatosensory cortex within the context of a selective attention task. Journal of Neurophysiology, 101, 2649–2667.Find this resource:
Merzenich, M. M., Kaas, J. H., Sur, M., & Lin, C.-S. (1978). Double representation of the body surface within cytoarchitectonic area 3b and 1 in “S1” in the owl monkey (Aotus Trivirgatus). The Journal of Comparative Neurology, 181, 41–73.Find this resource:
Mountcastle, V. B., Talbot, W. H., Sakata, H., & Hyvärinen, J. (1969). Cortical neuronal mechanisms in flutter-vibration studied in unanesthetized monkeys: Neuronal periodicity and frequency discrimination. Journal of Neurophysiology, 32, 452–484.Find this resource:
Okamoto, S., Nagano, H., & Yamada, Y. (2013). Psychophysical dimensions of tactile perception of textures. IEEE Transactions on Haptics, 6, 81–93.Find this resource:
Pack, C. C., & Bensmaia, S. J. (2015). Seeing and feeling motion: Canonical computations in vision and touch. PLoS Biology, 13(9), e1002271.Find this resource:
Padberg, J., Cerkevich, C., Engle, J., Rajan, A. T., Recanzone, G., Kaas, J., & Krubitzer, L. (2009). Thalamocortical connections of parietal somatosensory cortical fields in macaque monkeys are highly divergent and convergent. Cerebral Cortex, 19, 2038–2064.Find this resource:
Paré, M., Behets, C., & Cornu, O. (2003). Paucity of presumptive Ruffini corpuscles in the index finger pad of humans. The Journal of Comparative Neurology, 456, 260–266.Find this resource:
Paré, M., Smith, A. M., & Rice, F. L. (2002). Distribution and terminal arborizations of cutaneous mechanoreceptors in the glabrous finger pads of the monkey. The Journal of Comparative Neurology, 445, 347–359.Find this resource:
Paul, R. L., Merzenich, M., & Goodman, H. (1972). Representation of slowly and rapidly adapting cutaneous mechanoreceptors of the hand in Brodmann’s areas 3 and 1 of Macaca Mulatta. Brain Research, 36, 229–249.Find this resource:
Pei, Y.-C., Denchev, P. V., Hsiao, S. S., Craig, J. C., & Bensmaia, S. J. (2009a). Convergence of submodality-specific input onto neurons in primary somatosensory cortex. Journal of Neurophysiology, 102, 1843–1853.Find this resource:
Pei Y.-C., Denchev P. V., Hsiao, S. S., Craig, J. C., & Bensmaia, S. J. (2009b). Convergence of submodality-specific input onto neurons in primary somatosensory cortex. Journal of Neurophysiology, 102, 1843–1853.Find this resource:
Phillips, J., & Johnson, K. (1981). Tactile spatial resolution. II. Neural representation of bars, edges, and gratings in monkey primary afferents. Journal of Neurophysiology, 46(6), 1192–1203.Find this resource:
Phillips, J. R., Johansson, R. S., & Johnson, K. O. (1992). Responses of human mechanoreceptive afferents to embossed dot arrays scanned across fingerpad skin. Journal of Neuroscience, 12, 827–839.Find this resource:
Phillips, J. R., Johnson, K. O., & Hsiao, S. S. (1988). Spatial pattern representation and transformation in monkey somatosensory cortex. Proceedings of the National Academy of Sciences of the United States of America, 85, 1317–1321.Find this resource:
Picard, D., Dacremont, C., Valentin, D., & Giboreau, A. (2003). Perceptual dimensions of tactile textures. Acta Psychologica (Amst), 114, 165–184.Find this resource:
Portilla, J., & Simoncelli, E. P. (2000). A parametric texture model based on joint statistics of complex wavelet coefficients. International Journal of Computer Vision, 40, 49–71.Find this resource:
Randolph, M., & Semmes, J. (1974). Behavioral consequences of selective subtotal ablations in the postcentral gyrus of Macaca mulatta. Brain Research, 70, 55–70.Find this resource:
Roland, P. E., O’Sullivan, B., & Kawashima, R. (1998). Shape and roughness activate different somatosensory areas in the human brain. Proceedings of the National Academy of Sciences of the United States of America, 95, 3295–3300.Find this resource:
Romo, R., Hernández, A., Zainos, A., Lemus, L., & Brody, C. D. (2002). Neuronal correlates of decision-making in secondary somatosensory cortex. Nature Neuroscience, 5, 1217–1225.Find this resource:
Saal, H. P., & Bensmaia, S. J. (2014). Touch is a team effort: Interplay of submodalities in cutaneous sensibility. Trends in Neurosciences, 37, 689–697.Find this resource:
Saal, H. P., Delhaye, B. P., Rayhaun, B. C., & Bensmaia, S. J. (2017). Simulating tactile signals from the whole hand with millisecond precision. Proceedings of the National Academy of Sciences of the United States of America, 114(28), E5693–E5702.Find this resource:
Saal, H. P., Harvey, M. A., & Bensmaia, S. J. (2015). Rate and timing of cortical responses driven by separate sensory channels. Elife, 4, e10450.Find this resource:
Saal, H. P., Suresh, A. K., Solorzano, L. E., Weber, A. I., & Bensmaia, S. J. (2017). The effect of contact force on the responses of tactile nerve fibers to scanned textures. Neuroscience, 389, 99–103.Find this resource:
Saal, H. P., Wang, X., & Bensmaia, S. J. (2016). Importance of spike timing in touch: An analogy with hearing? Current Opinion in Neurobiology, 40, 142–149.Find this resource:
Salinas, E., Hernandez, A., Zainos, A., & Romo, R. (2000). Periodicity and firing rate as candidate neural codes for the frequency of vibrotactile stimuli. Journal of Neuroscience, 20, 5503–5515.Find this resource:
Sathian, K. (2016). Analysis of haptic information in the cerebral cortex. Journal of Neurophysiology, 116, 1795–1806.Find this resource:
Sathian, K., Goodwin, A. W., John, K. T., & Darian-Smith, I. (1989). Perceived roughness of a grating: Correlation with responses of mechanoreceptive afferents innervating the monkey’s fingerpad. Journal of Neuroscience, 9, 1273–1279.Find this resource:
Sathian, K., Lacey, S., Stilla, R., Gibson, G. O., Deshpande, G., Hu, X., LaConte, S., & Glielmi, C. (2011). Dual pathways for haptic and visual perception of spatial and texture information. Neuroimage, 57, 462–475.Find this resource:
Sathian, K., & Zangaladze, A. (1996). Tactile spatial acuity at the human fingertip and lip: Bilateral symmetry and interdigit variability. Neurology, 46, 1464–1466.Find this resource:
Scheibert, J., Leurent, S., Prevost, A., & Debregeas, G. (2009). The role of fingerprints in the coding of tactile information probed with a biomimetic sensor. Science, 323(5920), 1503–1506.Find this resource:
Servos, P., Lederman, S., Wilson, D., & Gati, J. (2001). fMRI-derived cortical maps for haptic shape, texture, and hardness. Cognitive Brain Research, 12, 307–313.Find this resource:
Simões-Franklin, C., Whitaker, T. A., & Newell, F. N. (2011). Active and passive touch differentially activate somatosensory cortex in texture perception. Human Brain Mapping, 32, 1067–1080.Find this resource:
Sinclair, R. J., & Burton, H. (1991). Neuronal activity in the primary somatosensory cortex in monkeys (Macaca mulatta) during active touch of textured surface gratings: Responses to groove width, applied force, and velocity of motion. Journal of Neurophysiology, 66, 153–169.Find this resource:
Sinclair, R. J., & Burton, H. (1993). Neuronal activity in the second somatosensory cortex of monkeys (Macaca mulatta) during active touch of gratings. Journal of Neurophysiology, 70, 331–350.Find this resource:
Skedung, L., Arvidsson, M., Chung, J. Y., Stafford, C. M., Berglund, B., & Rutland, M. W. (2013). Feeling small: Exploring the tactile perception limits. Scientific Reports, 3, 2617.Find this resource:
Smith, A. M., Chapman, C. E., Deslandes, M., Langlais, J. S., & Thibodeau, M. P. (2002). Role of friction and tangential force variation in the subjective scaling of tactile roughness. Experimental Brain Research, 144, 211–223.Find this resource:
Smith, A. M., & Scott, S. H. (1996). Subjective scaling of smooth surface friction. Journal of Neurophysiology, 75, 1957–1962.Find this resource:
Srinivasan, M. A., & LaMotte, R. H. (1995). Tactual discrimination of softness. Journal of Neurophysiology, 73, 88–101.Find this resource:
Sripati, A. P., Bensmaia, S. J., & Johnson, K. O. (2006). A continuum mechanical model of mechanoreceptive afferent responses to indented spatial patterns. Journal of Neurophysiology, 95, 3852–3864.Find this resource:
Sripati, A. P., Yoshioka, T., Denchev, P., Hsiao, S. S., & Johnson, K. O. (2006). Spatiotemporal receptive fields of peripheral afferents and cortical area 3b and 1 neurons in the primate somatosensory system. Journal of Neuroscience, 26, 2101–2114.Find this resource:
Stevens, S. S., & Harris, J. R. (1962). The scaling of subjective roughness and smoothness. Journal of Experimental Psychology - General, 64, 489–494.Find this resource:
Stilla, R., & Sathian K. (2008). Selective visuo-haptic processing of shape and texture. Human Brain Mapping, 29, 1123–1138.Find this resource:
Sur, M., Wall, J. T., & Kaas, J. H. (1984). Modular distribution of neurons with slowly adapting and rapidly adapting responses in area 3b of somatosensory cortex in monkeys. Journal of Neurophysiology, 51, 724–744.Find this resource:
Sutu, A., Meftah, E.-M., & Chapman, C. E. (2013). Physical determinants of the shape of the psychophysical curve relating tactile roughness to raised-dot spacing: Implications for neuronal coding of roughness. Journal of Neurophysiology, 109, 1403–1415.Find this resource:
Talbot, W. H., Darian-Smith, I., Kornhuber, H. H., & Mountcastle, V. B. (1968). The sense of flutter vibration comparison of the human capacity with response patterns of mechanoreceptive afferents from the monkey hand. Journal of Neurophysiology, 31, 301–304.Find this resource:
Taylor, M. M., & Lederman, S. J. (1975). Tactile roughness of grooved surfaces: A model and the effect of friction. Perception and Psychophysics, 17, 23–36.Find this resource:
Tremblay, F., Ageranioti-Bélanger, S. A., & Chapman, C. E. (1996). Cortical mechanisms underlying tactile discrimination in the monkey: I; Role of primary somatosensory cortex in passive texture discrimination. Journal of Neurophysiology, 76, 3382–3403.Find this resource:
Tymms, C., Zorin, D., & Gardner, E. P. (2017). Tactile perception of the roughness of 3D-printed textures. Journal of Neurophysiology, 119(3), 862–876.Find this resource:
Van Boven, R. W., & Johnson K. O. (1994). The limit of tactile spatial resolution in humans: Grating orientation discrimination at the lip, tongue, and finger. Neurology, 44, 2361–2366.Find this resource:
Vega-Bermudez, F., & Johnson, K. O. (1999). Surround suppression in the responses of primate SA1 and RA mechanoreceptive afferents mapped with a probe array. Journal of Neurophysiology, 81, 2711–2719.Find this resource:
Verrillo R. T., Bolanowski, S. J., & McGlone, F. P. (1999). Subjective magnitude of tactile roughness. Somatosensory and Motor Research, 16(4), 352–360.Find this resource:
Victor, J. D., & Purpura, K. P. (1996). Nature and precision of temporal coding in visual cortex: A metric-space analysis. Journal of Neurophysiology, 76(2), 1310–1326.Find this resource:
Weber, A. I., Saal, H. P., Lieber, J. D., Cheng, J.-W., Manfredi, L. R., Dammann, J. F., & Bensmaia, S. J. (2013). Spatial and temporal codes mediate the tactile perception of natural textures. Proceedings of the National Academy of Sciences of the United States of America USA, 110, 17107–17112.Find this resource:
Wheat, H. E., Goodwin, A. W., & Browning, A. S. (1995). Tactile resolution: Peripheral neural mechanisms underlying the human capacity to determine positions of objects contacting the fingerpad. Journal of Neuroscience, 15, 5582–5595.Find this resource:
Winfield, L., Glassmire, J., Colgate, J. E., & Peshkin, M. (2007). T-PaD: Tactile pattern display through variable friction reduction. In Proceedings - Second Joint EuroHaptics Conference and Symposium on Haptic Interfaces for Virtual Environment and Teleoperator Systems (pp. 421–426). Washington, DC: IEEE Computer Society.Find this resource:
Yau, J. M., Hollins, M., & Bensmaia, S. J. (2009). Textural timbre: The perception of surface microtexture depends in part on multimodal spectral cues. Communicative and Integrative Biology, 2, 344–346.Find this resource:
Yau, J. M., Kim, S. S., Thakur, P. H., & Bensmaia, S. J. (2016). Feeling form: The neural basis of haptic shape perception. Journal of Neurophysiology, 115(2), 631–642.Find this resource:
Yoshioka, T., Bensmaia, S. J., Craig, J. C., & Hsiao, S. S. (2007). Texture perception through direct and indirect touch: An analysis of perceptual space for tactile textures in two modes of exploration. Somatosensory and Motor Research, 24, 53–70.Find this resource:
Yoshioka, T., Craig, J. C., Beck, G. C., & Hsiao, S. S. (2011). Perceptual constancy of texture roughness in the tactile system. Journal of Neuroscience, 31, 17603–17611.Find this resource:
Yoshioka, T., Gibb, B., Dorsch, A. K., Hsiao, S. S., & Johnson, K. O. (2001). Neural coding mechanisms underlying perceived roughness of finely textured surfaces. Journal of Neuroscience, 21, 6905–6916.Find this resource:
Yoshioka, T., Gibb, B., Dorsch, A. K., Hsiao, S. S., & Johnson, K. O. (2001). Neural coding mechanisms underlying perceived roughness of finely textured surfaces. Journal of Neuroscience, 21, 6905–6916.Find this resource:
Zhang, H. Q., Murray, G. M., Coleman, G. T., Turman, A. B., Zhang, S. P., & Rowe, M. J. (2001). Functional characteristics of the parallel SI- and SII-projecting neurons of the thalamic ventral posterior nucleus in the marmoset. Journal of Neurophysiology, 85, 1805–1822.Find this resource:
Ziemba, C. M., Freeman, J., Movshon, J. A., & Simoncelli, E. P. (2016). Selectivity and tolerance for visual texture in macaque V2. Proceedings of the National Academy of Sciences of the United States of America, 113, E3140–E3149.Find this resource:
Ziemba, C. M., Freeman, J., Simoncelli, E. P., & Movshon, J. A. (2018). Contextual modulation of sensitivity to naturalistic image structure in macaque V2. Journal of Neurophysiology, 120(2), 409–420.Find this resource: