Neural computations in prosopagnosia.

We report an investigation of the neural processes involved in the processing of faces and objects of brain-lesioned patient PS, a well-documented case of pure acquired prosopagnosia. We gathered a substantial dataset of high-density electrophysiological recordings from both PS and neurotypicals. Using representational similarity analysis, we produced time-resolved brain representations in a format that facilitates direct comparisons across time points, different individuals, and computational models. To understand how the lesions in PS's ventral stream affect the temporal evolution of her brain representations, we computed the temporal generalization of her brain representations. We uncovered that PS's early brain representations exhibit an unusual similarity to later representations, implying an excessive generalization of early visual patterns. To reveal the underlying computational deficits, we correlated PS' brain representations with those of deep neural networks (DNN). We found that the computations underlying PS' brain activity bore a closer resemblance to early layers of a visual DNN than those of controls. However, the brain representations in neurotypicals became more akin to those of the later layers of the model compared to PS. We confirmed PS's deficits in high-level brain representations by demonstrating that her brain representations exhibited less similarity with those of a DNN of semantics.

Description of immature stages of Rhinusa species (Coleoptera, Curculionidae, Mecinini) with a focus on diagnostic morphological characters at the species and genus levels.

The mature larvae of the following fourteen Rhinusa species are described and illustrated: Rhinusaantirrhini (Paykull, 1800), R.asellus (Gravenhorst, 1807), R.collina (Gyllenhal, 1813), R.eversmanni (Rosenschoeld, 1838), R.florum (Rubsaamen, 1895), R.herbarum (H. Brisout de Barneville, 1862), R.incana (Kirsch, 1881), R.linariae (Panzer, 1796), R.melas (Boheman, 1838), R.neta (Germar, 1821), R.pilosa (Gyllenhal, 1838), R.rara Tosevski & Caldara, 2015, R.tetra (Fabricius, 1792), and R.vestita (Germar, 1821). The pupae of thirteen of them (except R.incana) were also described. The comparison of larval morphological characters and plant preferences provides evidence supporting the existence of different species groups previously established according to a phylogenetic analysis based on adult morphological characters. The following diagnostic attributes distinguishing the genus Rhinusa are highlighted. For the larvae: (1) pronotal shield indistinct; (2) thoracic prodorsal fold small or even vestigial; (3) abdominal postdorsal folds (especially of segments III-VII) high or even in the form of conical protuberances; (4) cuticle of abdominal segments densely covered with asperities; (5) cuticle without dark spots or dark pigmentation; (6) head suboval, rarely round; (7) labrum usually with 2 als; (8) des1 short or absent, rarely elongated; and (9) fs1-3 usually absent or minute. For the pupae: (1) body stout; (2) head protuberances always present; (3) pronotal protuberances (if present), separated at bases of the pronotum, always wider than higher; (4) abdominal protuberance usually present, wide or round; (5) femora usually with a single fes; and (6) urogomphi short or vestigial. Keys to the larvae and pupae described here are provided. All the characters used for identification are illustrated by photographs or drawings. Biological and distribution data, including new information, are provided for all the species studied.

Decoding face recognition abilities in the human brain.

Why are some individuals better at recognizing faces? Uncovering the neural mechanisms supporting face recognition ability has proven elusive. To tackle this challenge, we used a multimodal data-driven approach combining neuroimaging, computational modeling, and behavioral tests. We recorded the high-density electroencephalographic brain activity of individuals with extraordinary face recognition abilities-super-recognizers-and typical recognizers in response to diverse visual stimuli. Using multivariate pattern analyses, we decoded face recognition abilities from 1 s of brain activity with up to 80% accuracy. To better understand the mechanisms subtending this decoding, we compared representations in the brains of our participants with those in artificial neural network models of vision and semantics, as well as with those involved in human judgments of shape and meaning similarity. Compared to typical recognizers, we found stronger associations between early brain representations of super-recognizers and midlevel representations of vision models as well as shape similarity judgments. Moreover, we found stronger associations between late brain representations of super-recognizers and representations of the artificial semantic model as well as meaning similarity judgments. Overall, these results indicate that important individual variations in brain processing, including neural computations extending beyond purely visual processes, support differences in face recognition abilities. They provide the first empirical evidence for an association between semantic computations and face recognition abilities. We believe that such multimodal data-driven approaches will likely play a critical role in further revealing the complex nature of idiosyncratic face recognition in the human brain.

Recognizing facial expressions of emotion amid noise: A dynamic advantage.

Humans communicate internal states through complex facial movements shaped by biological and evolutionary constraints. Although real-life social interactions are flooded with dynamic signals, current knowledge on facial expression recognition mainly arises from studies using static face images. This experimental bias might stem from previous studies consistently reporting that young adults minimally benefit from the richer dynamic over static information, whereas children, the elderly, and clinical populations very strongly do (Richoz, Jack, Garrod, Schyns, & Caldara, 2015, Richoz, Jack, Garrod, Schyns, & Caldara, 2018b). These observations point to a near-optimal facial expression decoding system in young adults, almost insensitive to the advantage of dynamic over static cues. Surprisingly, no study has yet tested the idea that such evidence might be rooted in a ceiling effect. To this aim, we asked 70 healthy young adults to perform static and dynamic facial expression recognition of the six basic expressions while parametrically and randomly varying the low-level normalized phase and contrast signal (0%-100%) of the faces. As predicted, when 100% face signals were presented, static and dynamic expressions were recognized with equal efficiency with the exception of those with the most informative dynamics (i.e., happiness and surprise). However, when less signal was available, dynamic expressions were all better recognized than their static counterpart (peaking at ∼20%). Our data show that facial movements increase our ability to efficiently identify emotional states of others under the suboptimal visual conditions that can occur in everyday life. Dynamic signals are more effective and sensitive than static ones for decoding all facial expressions of emotion for all human observers.

The speed of race.

When asked to categorize faces according to 'race', people typically categorize other-race faces faster than faces belonging to their own race. This 'Other Race Categorization Advantage' is thought to reflect enhanced sensitivity to early visual signals characteristic of other-race faces, and can manifest within 200 ms of face presentation. However, recent research has highlighted the importance of signal intensity in this effect, where visual-degradation of the face images significantly enhances the effect and exposes a behavioural threshold at very low levels of visual quality where other-race visual signals are able to be perceived while same-race signals are not. The current study investigated the effect of signal intensity in race categorization processes in the brain through electroencephalography and in accuracy/reaction times. While replicating the previously observed enhancement of the other-race categorization advantage, we also found enhanced sensitivity to other-race faces in early P1 peaks, as well as later N170 and N250 peaks. These effects, however, related to the varying levels of signal intensity in the face stimuli, suggesting that race categorization may involve different types of perceptual and neural processes rather than one discrete process. The speed at which race is perceived depends on the intensity of the face signal.

Differences in eye movements for face recognition between Canadian and Chinese participants are not modulated by social orientation.

Face recognition strategies do not generalize across individuals. Many studies have reported robust cultural differences between West Europeans/North Americans and East Asians in eye movement strategies during face recognition. The social orientation hypothesis posits that individualistic vs. collectivistic (IND/COL) value systems, respectively defining West European/North American and East Asian societies, would be at the root of many cultural differences in visual perception. Whether social orientation is also responsible for such cultural contrast in face recognition remains to be clarified. To this aim, we conducted two experiments with West European/North American and Chinese observers. In Experiment 1, we probed the existence of a link between IND/COL social values and eye movements during face recognition, by using an IND/COL priming paradigm. In Experiment 2, we dissected the latter relationship in greater depth, by using two IND/COL questionnaires, including subdimensions to those concepts. In both studies, cultural differences in fixation patterns were revealed between West European/North American and East Asian observers. Priming IND/COL values did not modulate eye movement visual sampling strategies, and only specific subdimensions of the IND/COL questionnaires were associated with distinct eye-movement patterns. Altogether, we show that the typical contrast between IND/COL cannot fully account for cultural differences in eye movement strategies for face recognition. Cultural differences in eye movements for faces might originate from mechanisms distinct from social orientation.

A Taxonomic Revision of the Genus Cionus (Coleoptera, Curculionidae) from the Oriental Region.

Oriental species of the genus Cionus are herein revised for the first time. Eight species are recognized as distinct based on morphological characters of adults. One species is described as new: C. ottomerkli sp. nov., from India, whereas the name vossi (nom. nov.) is proposed for Cionus flavoguttatus Voss, 1957 (not Stierlin, 1893). The following new synonymy is established: Cionus indicus Desbrochers des Loges, 1890 (=Cionus albosparsus Faust, 1898 syn. nov.). Lectotypes of Cionus albosparsus Faust, 1898; Cionus flavoguttatus Voss, 1957; Cionus indicus Desbrochers des Loges, 1890; Cionus obesus Pascoe, 1883; and Cionus tonkinensis Wingelmüller, 1915, are designated.

A TAXONOMIC REVISION OF THE AFROTROPICAL SPECIES OF THE WEEVIL GENUS CIONUS (COLEOPTERA: CURCULIONIDAE).

The Afrotropical species of the genus Cionus Clairville, 1798 are revised and 52 species are recognized as valid. Thirty-one species are described as new to the science: twenty-five from the continental subregions (C. concavifrons sp. n., C. coniungens sp. n., C. cretaceus sp. n., C. diaboli sp. n., C. fimbriatus sp. n., C. frater sp. n., C. friedmani sp. n., C. geometricus sp. n., C. hirtellus sp. n., C. intermedius sp. n., C. latruncularius sp. n., C. limosus sp. n., C. longinasus sp. n., C. mimeticus sp. n., C. natalensis sp. n., C. nhlosanicus sp. n., C. oberprieleri sp. n., C. oculatus sp. n., C. schuelei sp. n., C. stalsi sp. n., C. tanzanicus sp. n., C. tenuepilosus sp. n., C. terrosus sp. n., C. transvaalicus sp. n., C. zimbabwicus sp. n.) and six from Madagascar (C. callosus sp. n., C. convexiusculus sp. n., C. guttula sp. n., C. planus sp. n., C. variolosus sp. n., C. verrucosus sp. n.). The following new synonymies are proposed: Cionus chilianthi Marshall, 1941 syn. n. of C. angulicollis Rosenschoeld, 1838, C. virgatus Rosenschoeld, 1838 syn. n. and C. decorus Boheman, 1845 syn. n. of C. nubilosus Rosenschoeld, 1838, C. leucostictus griseus Fairmaire 1903 syn. n. of C. leucostictus Fairmaire, 1897. Lectotypes of Cionus albidus Rosenschoeld, 1838, C. alluaudi Hustache, 1920, C. angulicollis Rosenschoeld, 1838, C. catenatus Fairmaire, 1897, C. compactus Fairmaire, 1903, C. coriaceus Fairmaire, 1903, C. decorus Boheman, 1845, C. ebeninus Hustache, 1956, C. histrio Rosenschoeld, 1838, C. ingratus Fåhraeus, 1871, C. leucostictus Fairmaire, 1897, C. leucostictus griseus Fairmaire, 1903, C. notatus Rosenschoeld, 1838, C. nubilosus Rosenschoeld, 1838, C. perlatus Faust, 1885, C. pustulatus Fåhraeus, 1871, C. tristis Boheman, 1838, C. usambicus Faust, 1889, C. vicarius Hustache, 1939 and C. virgatus Rosenschoeld, 1838 are designated. The "variety" maculithorax Voss, 1960 of Cionus pardus Marshall, 1941 is considered an unavailable name. Description or redescription, comparative morphology, distribution, biological notes and key to all Afrotropical species are given. Photos of habitus in dorsal, of aedeagus in ventral and lateral, and of the apex of penis in dorsal view are reported for each species.

Cultural Differences in Inhibitory Control: An ALE Meta-Analysis.

Culture greatly influences our attitudes, beliefs, and behaviors, affecting how we communicate and make decisions. There is an ongoing debate regarding the belief that people from Eastern cultures possess greater self-control abilities when compared to people from Western cultures. In this study, we conducted a meta-analysis using the Activation Likelihood Estimation (ALE) algorithm to compare 30 studies (719 subjects, 373 foci) that used fMRI to investigate the performance in Go-Nogo and Stop Signal Tasks of participants from Western and/or Eastern countries. Our meta-analysis found differences between the networks activated in Eastern and Western culture participants. The right prefrontal cortex showed distinct patterns, with the Inferior Frontal gyrus more active in the Eastern group and the middle and superior frontal gyri more active in the Western group. Our findings suggest that Eastern culture subjects have a higher tendency to activate brain regions involved in proactive inhibitory control, while Western culture subjects rely more on reactive inhibitory brain regions during cognitive control tasks. This implies that proactive inhibition may play a crucial role in promoting the collective and interdependent behavior typical of Eastern cultures, while reactive inhibition may be more important for efficient cognitive control in subjects of Western cultures that prioritize individualism and independence.

Developmental eye movement strategies for decoding facial expressions of emotion.

In our daily lives, we routinely look at the faces of others to try to understand how they are feeling. Few studies have examined the perceptual strategies that are used to recognize facial expressions of emotion, and none have attempted to isolate visual information use with eye movements throughout development. Therefore, we recorded the eye movements of children from 5 years of age up to adulthood during recognition of the six "basic emotions" to investigate when perceptual strategies for emotion recognition become mature (i.e., most adult-like). Using iMap4, we identified the eye movement fixation patterns for recognition of the six emotions across age groups in natural viewing and gaze-contingent (i.e., expanding spotlight) conditions. While univariate analyses failed to reveal significant differences in fixation patterns, more sensitive multivariate distance analyses revealed a U-shaped developmental trajectory with the eye movement strategies of the 17- to 18-year-old group most similar to adults for all expressions. A developmental dip in strategy similarity was found for each emotional expression revealing which age group had the most distinct eye movement strategy from the adult group: the 13- to 14-year-olds for sadness recognition; the 11- to 12-year-olds for fear, anger, surprise, and disgust; and the 7- to 8-year-olds for happiness. Recognition performance for happy, angry, and sad expressions did not differ significantly across age groups, but the eye movement strategies for these expressions diverged for each group. Therefore, a unique strategy was not a prerequisite for optimal recognition performance for these expressions. Our data provide novel insights into the developmental trajectories underlying facial expression recognition, a critical ability for adaptive social relations.

Prosopagnosia does not abolish other-race effects.

Healthy observers recognize more accurately same-than other-race faces (i.e., the Same-Race Recognition Advantage - SRRA) but categorize them by race more slowly than other-race faces (i.e., the Other-Race Categorization Advantage - ORCA). Several fMRI studies reported discrepant bilateral activations in the Fusiform Face Area (FFA) and Occipital Face Area (OFA) correlating with both effects. However, due to the very nature and limits of fMRI results, whether these face-sensitive regions play an unequivocal causal role in those other-race effects remains to be clarified. To this aim, we tested PS, a well-studied pure case of acquired prosopagnosia with lesions encompassing the left FFA and the right OFA. PS, healthy age-matched and young adults performed two recognition and three categorization by race tasks, respectively using Western Caucasian and East Asian faces normalized for their low-level properties with and without-external features, as well as in naturalistic settings. As expected, PS was slower and less accurate than the controls. Crucially, however, the magnitudes of her SRRA and ORCA were comparable to the controls in all the tasks. Our data show that prosopagnosia does not abolish other-race effects, as an intact face system, the left FFA and/or right OFA are not critical for eliciting the SRRA and ORCA. Race is a strong visual and social signal that is encoded in a large neural face-sensitive network, robustly tuned for processing same-race faces.

Stimulus size modulates idiosyncratic neural face identity discrimination.

Humans show individual differences in neural facial identity discrimination (FID) responses across viewing positions. Critically, these variations have been shown to be reliable over time and to directly relate to observers' idiosyncratic preferences in facial information sampling. This functional signature in facial identity processing might relate to observer-specific diagnostic information processing. Although these individual differences are a valuable source of information for interpreting data, they can also be difficult to isolate when it is not possible to test many conditions. To address this potential issue, we explored whether reducing stimulus size would help decrease these interindividual variations in neural FID. We manipulated the size of face stimuli (covering 3°, 5°, 6.7°, 8.5°, and 12° of visual angle), as well as the fixation location (left eye, right eye, below the nasion, nose, and mouth) while recording electrophysiological responses. Same identity faces were presented with a base frequency of 6 Hz. Different identity faces were periodically inserted within this sequence to trigger an objective index of neural FID. Our data show robust and consistent individual differences in neural face identity discrimination across viewing positions for all face sizes. Nevertheless, FID was optimal for a larger number of observers when faces subtended 6.7° of visual angle and fixation was below the nasion. This condition is the most suited to reduce natural interindividual variations in neural FID patterns, defining an important benchmark to measure neural FID when it is not possible to assess and control for observers' idiosyncrasies.

Race categorization in noise.

People are typically faster to categorize the race of a face if it belongs to a race different from their own. This Other Race Categorization Advantage (ORCA) is thought to reflect an enhanced sensitivity to the visual race signals of other race faces, leading to faster response times. The current study investigated this sensitivity in a cross-cultural sample of Swiss and Japanese observers with a race categorization task using faces that had been parametrically degraded of visual structure, with normalized luminance and contrast. While Swiss observers exhibited an increasingly strong ORCA in both reaction time and accuracy as the face images were visually degraded up to 20% structural coherence, the Japanese observers manifested this pattern most distinctly when the faces were fully structurally-intact. Critically, for both observer groups, there was a clear accuracy effect at the 20% structural coherence level, indicating that the enhanced sensitivity to other race visual signals persists in significantly degraded stimuli. These results suggest that different cultural groups may rely on and extract distinct types of visual race signals during categorization, which may depend on the available visual information. Nevertheless, heavily degraded stimuli specifically favor the perception of other race faces, indicating that the visual system is tuned by experience and is sensitive to the detection of unfamiliar signals.

In search of some type-specimens of Rhamphus [Clairville], 1798 (Coleoptera: Curculionidae).

During morphological and molecular studies of species of Rhamphus from southern and western Europe, the authors realized that some specimens currently identified as R. pulicarius (Herbst, 1795) and R. oxyacanthae (Marsham, 1802), two widely distributed species in Europe, belonged to different closely related taxa. Therefore, it was necessary to examine type specimens of these and other species considered synonymous or confused with them. It was possible to designate lectotypes for Rhamphus subaeneus Illiger, 1808 and Rhamphus kiesenwetteri Tournier, 1873. However, it was necessary to designate neotypes for: Curculio pulicarius Herbst, 1795, Curculio oxyacanthae Marsham, 1802 and Rhamphus flavicornis [Clairville], 1798. These three neotypes were sequenced for mtCOI and the sequences are now accessible online. Moreover, in accordance with Article 23.9 and the Principle of Priority of the Code, because of confirmed synonymy between R. oxyacanthae and R. flavicornis, the former name is officially proposed as nomen protectum and the latter as nomen oblitum. Detailed information regarding historical entomological collections in the Museum fr Naturkunde der Humboldt-Universitt of Berlin and the Clairville collection in the Naturhistorisches Museum of Basel, relating to our search for relevant type specimens, is provided.

Description of immature stages of Gymnetron species (Coleoptera, Curculionidae, Curculioninae), with particular emphasis on the diagnostic morphological characters at the generic and specific levels.

The immature stages of the following five Palaearctic Gymnetron species are described for the first time: G.tibiellum Desbrochers des Loges, 1900, G.veronicae (Germar, 1821), G.rotundicolle Gyllenhal, 1838, G.melanarium (Germar, 1821), and G.villosulum Gyllenhal, 1838. These species belong to four different groups previously established according to a phylogenetic analysis: the first two belong to the G.veronicae group and the other three to groups respectively bearing their name (G.rotundicolle, G.melanarium, and G.villosulum groups). All these species exhibit several diagnostic characters distinguishing them from each other. Some characters that can be used to separate Gymnetron from other genera in the tribe are also suggested. Three highly significant characters for the larvae and three for the pupae were identified. For the larvae they are: (1) labial palpi with single palpomeres, (2) all spiracles unicameral, and (3) epipharynx with a single pair of mes or none at all. For the pupae they are: (1) the pronotum with prominent pronotal protuberances, (2) abdominal segment VIII with a conical abdominal protuberance dorsally, and (3) very short or even reduced urogomphi. The species studied here are compared with those Gymnetron species already known and with other genera in the tribe Mecinini. Keys to the larvae and pupae described here are provided. All the characters used for identification are illustrated by photographs or drawings.

Rapid saccadic categorization of other-race faces.

The human visual system is very fast and efficient at extracting socially relevant information from faces. Visual studies employing foveated faces have consistently reported faster categorization by race response times for other-race compared with same-race faces. However, in everyday life we typically encounter faces outside the foveated visual field. In study 1, we explored whether and how race is categorized extrafoveally in same- and other-race faces normalized for low-level properties by tracking eye movements of Western Caucasian and East Asian observers in a saccadic response task. The results show that not only are people sensitive to race in faces presented outside of central vision, but the speed advantage in categorizing other-race faces occurs astonishingly quickly in as little as 200 ms. Critically, this visual categorization process was approximately 300 ms faster than the typical button press responses on centrally presented foveated faces. Study 2 investigated the genesis of the extrafoveal saccadic response speed advantage by comparing the influences of the response modality (button presses and saccadic responses), as well as the potential contribution of the impoverished low-spatial frequency spectrum characterizing extrafoveal visual information processing. Button press race categorization was not significantly faster with reconstructed retinal-filtered low spatial frequency faces, regardless of the visual field presentation. The speed of race categorization was significantly boosted only by extrafoveal saccades and not centrally foveated faces. Race is a potent, rapid, and effective visual signal transmitted by faces used for the categorization of ingroup/outgroup members. This fast universal visual categorization can occur outside central vision, igniting a cascade of social processes.

On the Affinities and Systematic Position of Lachnaeus Schoenherr and Rhinocyllus Germar in the Tribe Lixini (Coleoptera: Curculionidae: Lixinae) Based on the Morphological Characters of the Immature Stages.

Mature larvae and pupae of Lachnaeus crinitus Schoenherr, 1826 and Rhinocyllus alpinus Gültekin, Diotti and Caldara, 2019 and pupae of R. conicus (Frölich, 1792), belonging to the Lixini (Curculionidae: Lixinae), are morphologically described for the first time. They possess all the characters considered distinctive in the immature stages of this tribe and are distinguishable from all the related genera by a combination of some characters (e.g., presence of endocarina, shape of premental sclerite; the number of pds on the abdominal segments; size and presence of urogomphi). It is emphasized that the controversial tribe Rhinocyllini is not supported by the characters of the larvae and pupae of Rhinocyllus and that the two subgenera of this genus, Rhinocyllus s. str. and Rhinolarinus, are separable from each other not only by characters of the adult but also distinctive characters of the larvae and pupae. These results confirm that the morphology of the immature stages, which is usually overlooked, can be very important for the purpose of identifying new characters that are useful for clarifying taxonomical and phylogenetic complex situations based only on the study of the imagoes.

Description of two new species of Rhamphus related to R. oxyacanthae (Curculionidae, Curculioninae, Rhamphini) from Italy based on a morphological study supported by molecular data.

Two new species of the weevil genus Rhamphus from Italy are herein described: R. bavierai n. sp. (Sicily) and R. hampsicora n. sp. (Sardinia). Both are morphologically and from a molecular perspective close to R. oxyacanthae (Marsham, 1802) and R. monzinii Pesarini Diotti, 2012. Aside from a diagnostic description and a synoptic key, distribution data and notes on the host plants of the four species are reported. Whereas R. monzinii can be distinguished by several morphological characters, the other three species are morphologically very similar to each other and separable only by the combination of a few subtle characters. On the contrary, a preliminary molecular study revealed substantial divergences of mtCOI from 6.2 to 14.9% between the species, confirming the importance of an integrative taxonomy.

The recognition of facial expressions of emotion in deaf and hearing individuals.

During real-life interactions, facial expressions of emotion are perceived dynamically with multimodal sensory information. In the absence of auditory sensory channel inputs, it is unclear how facial expressions are recognised and internally represented by deaf individuals. Few studies have investigated facial expression recognition in deaf signers using dynamic stimuli, and none have included all six basic facial expressions of emotion (anger, disgust, fear, happiness, sadness, and surprise) with stimuli fully controlled for their low-level visual properties, leaving the question of whether or not a dynamic advantage for deaf observers exists unresolved. We hypothesised, in line with the enhancement hypothesis, that the absence of auditory sensory information might have forced the visual system to better process visual (unimodal) signals, and predicted that this greater sensitivity to visual stimuli would result in better recognition performance for dynamic compared to static stimuli, and for deaf-signers compared to hearing non-signers in the dynamic condition. To this end, we performed a series of psychophysical studies with deaf signers with early-onset severe-to-profound deafness (dB loss >70) and hearing controls to estimate their ability to recognize the six basic facial expressions of emotion. Using static, dynamic, and shuffled (randomly permuted video frames of an expression) stimuli, we found that deaf observers showed similar categorization profiles and confusions across expressions compared to hearing controls (e.g., confusing surprise with fear). In contrast to our hypothesis, we found no recognition advantage for dynamic compared to static facial expressions for deaf observers. This observation shows that the decoding of dynamic facial expression emotional signals is not superior even in the deaf expert visual system, suggesting the existence of optimal signals in static facial expressions of emotion at the apex. Deaf individuals match hearing individuals in the recognition of facial expressions of emotion.

Description and biological notes of the larva of Cionus olivieri Rosenschoeld, 1838 (Coleoptera, Curculionidae), with a comparison with other species of the tribe Cionini.

The mature larva of Cionus olivieri Rosenschoeld, 1838 is described and illustrated in detail for the first time. It is compared with those known from the same genus and other genera in the tribe Cionini and with those of the hypothesized sister tribe Mecinini in the Curculioninae. The larvae of Cionus have three distinctive diagnostic features: the reduced number of setae on the epicranium (only two or three des and one or two fs) and on the epipharyngeal lining (only two als, two ams, and no mes); i.e., distinctly fewer than the most frequent number of setae in weevils, and mandibles dentate or angulate internally near the base. If considered together with Stereonychus Suffrian, 1854, the other genus of Cionini with larvae studied in detail, it is preliminarily suggested that mature larvae of this tribe might be characterized by six main diagnostic features: (1) labial palpi one-segmented, (2) labral rods absent, (3) pedal areas swollen to form large lobes or prolegs, (4) mandible with sharp apical teeth, (5) reduced number of fs on frons, only one or two fs, and (6) reduced number of epipharyngeal setae (two or three als and two or three ams, but no mes). It was noticed that C. helleri Reitter, 1904 from Japan, a very distinct species in the genus for some characters of the adult, also possesses distinctive characters in the larva which are uncommon among known cionines. New biological data on C. olivieri with the discovery of its host plant, Verbascum songaricum (Scrophulariaceae), in central Asia are also reported.