Odogenic change of blood coagulation in humans.

The blood coagulation time as an integral sign of human homeostasis is revealed to be influenced by conscious or unconscious olfactory stimuli through autonomic mechanisms. The hemostasis of subjects with predominance of sympathetic activity is more sensitive to the olfactory stimuli than that of subjects with vagal prevalence. The effects of the olfactory stimuli upon hemostasis in humans support the viewpoint that simultaneous information and physico-chemical processes act together in parallel to play and important role in life activities of human organism (Simonov, 1981; Sudakov, 1995). Emotions, therefore, are essential in the transfer of information from the environment (Anokhin, 1966; Miltner et al., 1994). It is not excluded that even very weak stimuli which are subthreshold for conscious perception might be informational for the organism as those engaging emotional response.     

A delivery system for olfactory stimuli

This paper describes the design of a new method for controlling and administering olfactory stimuli—namely, thehood system. The hood system involves a stream of vaporized odor (at known concentrations) mixed with odorless air and pumped (at a constant flow rate) into an oxygen therapy hood. It is designed to be used with odorants in solution, such as essential oils, as the olfactory stimulus. The use of oxygen therapy hoods allows for the precise control of a constant concentration of odorized air over time, while allowing subjects to breathe normally. The hood system provides a natural administration of olfactory stimuli and the exact determination of the stimulus concentration. The use of this system will allow experimental conditions to be completely defined and results and replication studies to be accurately interpreted. The hood system is portable, cost effective, and constructed from readily available components. It is proposed that the hood system could be adopted to suit a wide range of olfactory research, particularly that in which the effects of chronic exposure to olfactory stimuli on cognition are examined.     

Olfactory working memory: effects of verbalization on the 2-back task

Working memory for odors, which has received almost no attention in the literature, was investigated in two experiments. We show that performance in a 2-back task with odor stimuli is well above chance. This is true not only for highly familiar odors, as has been shown by Dade, Zatorre, Evans, and Jones-Gotman, NeuroImage, 14, 650–660, (2001), but also for unfamiliar ones that are notoriously difficult to name. We can conclude that information about an olfactory stimulus can be retained in the short term and can continuously be updated for comparison with new olfactory probes along the lines of a functional odor working memory. However, the performance in the working memory task is highly dependent on participants’ verbalization of the odor. In addition, results indicated that odor working memory performance is dependent on the ability to discriminate among the odor stimuli (Experiment 2). The results are discussed in relation to recent ideas of a separate olfactory working memory slave system.     

Non-visual consciousness and visual images in blindsight

In a recent response paper to Brogaard (2011a), Morten Overgaard and Thor Grünbaum argue that my case for the claim that blindsight subjects are not visually conscious of the stimuli they correctly identify rests on a mistaken necessary criterion for determining whether a conscious experience is visual or non-visual. Here I elaborate on the earlier argument while conceding that the question of whether blindsight subjects are visually conscious of the visual stimuli they correctly identify largely is an empirical question. I conclude by sketching a method for testing whether blindsight subjects have visual consciousness of stimuli presented to them in their blind field.     

Links between conscious awareness and response inhibition: evidence from masked priming

Recent results from “subliminal priming” experiments have shown that masked prime stimuli which can not be consciously perceived can trigger response activation processes, but that these response activations can later be subject to inhibition. Links between conscious awareness and response inhibition were investigated by manipulating the visibility of masked prime stimuli, from clearly visible primes to prime stimuli that were inaccessible to conscious perception. Response inhibition was observed with unperceived prime stimuli, but not for suprathreshold primes. Correlations between individual prime identification thresholds and the onset of response inhibition indicate that the absence or presence of conscious awareness can predict whether or not response inhibition is elicited. These results demonstrate qualitative differences in the effects of conscious and unconscious information. It is argued that response facilitation produced by consciously available perceptual information can counteract automatic effects of self-inhibitory motor control circuits.     

Gender differences in implicit and explicit processing of emotional facial expressions as revealed by event-related theta synchronization

Emotion information processing may occur in 2 modes that are differently represented in conscious awareness. Fast online processing involves coarse-grained analysis of salient features and is not represented in conscious awareness; offline processing takes hundreds of milliseconds to generate fine-grained analysis and is represented in conscious awareness. These processing modes may be studied using event-related electroencephalogram theta synchronization as a marker of emotion processing. Two experiments were conducted that differed on the mode of emotional information presentation. In the explicit mode, subjects were explicitly instructed to evaluate the emotional content of presented stimuli; in the implicit mode, their attention was directed to other features of the stimulus. In the implicit mode, theta synchronization was most pronounced in the early processing stage, whereas in the explicit mode, it was more pronounced in the late processing stage. The early processing stage was more pronounced in men, whereas the late processing stage was more pronounced in women. Implications of these gender differences in emotion processing for well-documented differences in social behavior are discussed.     

Informational and neural adaptation curves are asynchronous

Norwich’s entropy theory of perception (plus a few additional assumptions) suggests the existence of an “informational adaptation curve” (change in stimulus equivocation with stimulus duration) for suprathreshold prothetic stimuli that is synchronous with the “neural adaptation curve” (change in firing rate with stimulus duration) observed for sensory neurons. Five experiments are reported in which informational adaptation curves were measured for auditory and visual stimuli by having subjects make absolute identifications of suprathreshold sound or light intensities of various durations. Information transmissions for the shortest duration stimuli (1 and 5 msec, respectively, for light and sound) were surprisingly large (small equivocations), indicating that intensity information is acquired very rapidly by the whole organism. The equations of entropy theory were fitted to adaptation data for peripheral sensory neurons (spiral ganglion cells and retinal ganglion cells) and were compared to the informational adaptation curves. It was found that informational adaptation occurred more rapidly than neural adaptation. That is, the two types of adaptation process are asynchronous. However, for both audition and vision, the total amount of information mediated by the adaptation process (channel capacity) was-about the same for both types of processes (2.03 bits vs. 2.1 bits per stimulus for sound intensity; 1.3 vs. 2.0 bits per stimulus for light intensity). Faster acquisition could be accomplished in the whole organism through convergent neural circuits that increase sampling, rate-by pooling the samples taken by individual receptor systems     

Informational and neural adaptation curves are asynchronous.

Norwich's entropy theory of perception (plus a few additional assumptions) suggests the existence of an "infromational adaptation curves" (change in stimulus equivocation with stimulus duration) for suprathreshold prothetic stimuli that is synchronous with the "neural adaptation curve" (change in firing rate with stimulus duration) observed for sensory neurons. Five experiments are reported in which informational adaptation curves were measured for auditory and visual stimuli by having subjects make absolute identifications of suprathreshold sound or light intenstiies of various durations. Information transmissions for the shortest duration stimuli (1 and 5 msec, respectively, for light and sound) were surprisingly large (small equivocations), indicating that intensity information is acquired very rapidly by the whole organism. The equations of entropy theory were fitted to adaptation data for peripheral sensory neurons (spiral ganglion cells and retinal ganglion cells) and were compared to the informational adaptation curves. It was found that informational adaptation occurred more rapidly than neural adaptation. That is, the two types of adaptation process are asynchronous. However, for both audition and vision, the total amount of information mediated by the adaptation process (channel capacity) was about the same for both types of processes (2.03 bits vs. 2.1 bits per stimulus for sound intensity; 1.3 vs. 2.0 bits per stimulus for light intensity). Faster acquisition could be accomplished in the whole organism through convergent neural circuits that increase sampling rate by pooling the samples taken by individual receptor systems.     

The Timing of Conscious Experience: A Critical Review and Reinterpretation of Libet''s Research

An extended examination of Libet's works led to a comprehensive reinterpretation of his results. According to this reinterpretation, the Minimum Train Duration of electrical brain stimulation should be considered as the time needed to create a brain stimulus efficient for producing conscious sensation and not as a basis for inferring the latency for conscious sensation of peripheral origin. Latency for conscious sensation with brain stimulation may occurafterthe Minimum Train Duration. Backward masking with cortical stimuli suggests a 125–300 ms minimum value for the latency for conscious sensation of threshold skin stimuli. Backward enhancement is not suitable for inferring this latency. For determining temporal relations between stimuli that correspond to subjects' reports, theendof cerebral Minimum Train Duration should be used as reference, rather than its onset. Results of coupling peripheral and cortical stimuli are explained by a latency after the cortical Minimum Train Duration, having roughly the same duration as the latency for supraliminal skin stimuli. Results of coupling peripheral stimuli and stimuli to medial lemniscus (LM) are explained by a shorter LM latency and/or a longer peripheral latency. This interpretation suggests a 230 ms minimum value for the latency for conscious sensation of somatosensory near-threshold stimuli. The backward referral hypothesis, as formulated by Libet, should not be retained. Long readiness potentials preceding spontaneous conscious or nonconscious movements suggest that both kinds of movement are nonconsciously initiated. The validity of Libet's measures of W and M moments (Libet et al., 1983a) is questionable due to problems involving latencies, training, and introspective distinction of W and M. Veto of intended actions may be initially nonconscious but dependent on conscious awareness.     

Animalism and the varieties of conjoined twinning

We defend the view that we are not identical to organisms against the objection that it implies that there are two subjects of every conscious state one experiences: oneself and one’s organism. We then criticize animalism—the view that each of us is identical to a human organism—by showing that it has unacceptable implications for a range of actual and hypothetical cases of conjoined twinning: dicephalus, craniopagus parasiticus, and cephalopagus.     

The relationship between feature binding and consciousness: evidence from asynchronous multi-modal stimuli

Processing the various features from different feature maps and modalities in coherent ways requires a dedicated integration mechanism (“the binding problem”). Many authors have related feature binding to conscious awareness but little is known about how tight this relationship really is. We presented subjects with asynchronous audiovisual stimuli and tested whether the two features were integrated. The results show that binding took place up to 350 ms feature-onset asynchronies, suggesting that integration covers a relatively wide temporal window. We also asked subjects to explicitly judge whether the two features would belong to the same or to the different events. Unsurprisingly, synchrony judgments decreased with increasing asynchrony. Most importantly, feature binding was entirely unaffected by conscious experience: features were bound whether they were experienced as occurring together or as belonging to a separate events, suggesting that the conscious experience of unity is not a prerequisite for, or a direct consequence of binding.     

Sex differences in memory performance for odors, tone sequences and colors

Sense of olfaction would seem to be of little importance for human behavior. However, a closer look at this from the psychological point of view reveals many interesting aspects, such as sex differences in olfactory perception, that are of interest to differential psychology. The present study deals with sex differences in the memory for odors; we assume that women will do better here than men while other memory tasks involving acoustical and optical stimuli will show no such differences. Sixty women and 40 men were examined. On the first day, they had to retain 10 odors, 10 random-generated tone-sequences, and 10 colors. On the second day, 20 such stimuli for each memory task were presented, and the subjects had to remember and to tell which were known and which of them were unknown stimuli to them. A significant advantage in the olfaction memory task was found for women, while acoustical and optical memory scores showed no such differences. This expected finding is discussed in two ways. First, the female advantage might result from phylogenetic sources. Second, it might arise because women in general more often than men seem to deal with olfactory cues, so that they might simply have more experience and therefore the greater chance to score higher in an odor memory task.     

Unconscious task application

The nature of unconscious information processing is a heavily debated issue in cognitive science (e.g., Kouider & Dehaene, 2007), and neuroscience (e.g., Crick & Koch, 1998). Traditionally, it has been thought that unconscious cognitive processing is restricted to knowledge that is strongly prepared by conscious processes (e.g., Dehaene et al., 1998). In three experiments, we show that the task that is performed consciously can also be applied unconsciously to items outside the current task set. We found that a same–different judgment of two target stimuli was also performed on two subliminally presented prime stimuli. This was true for target and prime stimuli from entirely different categories, as well as for prime and target stimuli at different levels of abstraction. These results reveal that unconscious processing can generalize more widely than previously accepted.     

Facial reactions to emotional stimuli: Automatically controlled emotional responses

Based on a model in which the facial muscles can be both automatically/involuntarily controlled and voluntarily controlled by conscious processes, we explore whether spontaneously evoked facial reactions can be evaluated in terms of criteria for what characterises an automatic process. In three experiments subjects were instructed to not react with their facial muscles, or to react as quickly as possible by wrinkling the eyebrows (frowning) or elevating the cheeks (smiling) when exposed to pictures of negative or positive emotional stimuli, while EMG activity was measured from the corrugator supercilii and zygomatic major muscle regions. Consistent with the proposition that facial reactions are automatically controlled, the results showed that the corrugator muscle reaction was facilitated to negative stimuli and the zygomatic muscle reaction was facilitated to positive stimuli. The results further showed that, despite the fact that subjects were required to not react with their facial muscles at all, they could not avoid producing a facial reaction that corresponded to the negative and positive stimuli.     

Repetition blindness is immune to the central bottleneck

Theattentional blink (AB) andrepetition blindness (RB) phenomena refer to subjects’ impaired ability to detect the second of two different (AB) or identical (RB) target stimuli in a rapid serial visual presentation stream if they appear within 500 msec of one another. Despite the fact that the AB reveals a failure of conscious visual perception, it is at least partly due to limitations at central stages of information processing. Do all attentional limits to conscious perception have their locus at this central bottleneck? To address this question, here we investigated whether RB is affected by online response selection, a cognitive operation that requires central processing. The results indicate that, unlike the AB, RB does not result from central resource limitations. Evidently, temporal attentional limits to conscious perception can occur at multiple stages of information processing.     

Verbal versus olfactory cues: affect in elicited memories

Verbal processing has a reduced role for olfactory stimuli. It is difficult to provide a label for an odor experience. Odor perception can retrieve memories of life events with personal meaning and elicit affective experiences. Odors that have emotionally loaded content could produce older memories. Common odors with well-known names have been used. In Exp. 1 the names were shown, and the subjects were asked to imagine the corresponding odors; subsequently those odorants were presented. In Exp. 2 at first the odorants were presented and subsequently their names, printed one each per white card. The subjects were requested to provide written free associations. At the end of each session they scored a semantic differential. The hypothesis that emotionally loaded associations are more frequent when evoked by odorants seems confirmed, supported also by some reliable differences between the profiles for olfactory verbal stimuli. The evaluation of olfactory stimuli did not differ from one experiment to the other; verbal stimuli, on the contrary, are differently evaluated if the corresponding odorants were presented before or after their labels.     

Are there unconscious perceptual processes?

Blindsight and vision for action seem to be exemplars of unconscious visual processes. However, researchers have recently argued that blindsight is not really a kind of unconscious vision but is rather severely degraded conscious vision. Morten Overgaard and colleagues have recently developed new methods for measuring the visibility of visual stimuli. Studies using these methods show that reported clarity of visual stimuli correlates with accuracy in both normal individuals and blindsight patients. Vision for action has also come under scrutiny. Recent findings seem to show that information processed by the dorsal stream for online action contributes to visual awareness. Some interpret these results as showing that some dorsal stream processes are conscious visual processes (e.g., Gallese, 2007; Jacob & Jeannerod, 2003). The aim of this paper is to provide new support for the more traditional view that blindsight and vision for action are genuinely unconscious perceptual processes. I argue that individuals with blindsight do not have access to the kind of purely qualitative color and size information which normal individuals do. So, even though people with blindsight have a kind of cognitive consciousness, visual information processing in blindsight patients is not associated with a distinctly visual phenomenology. I argue further that while dorsal stream processing seems to contribute to visual awareness, only information processed by the early dorsal stream (V1, V2, and V3) is broadcast to working memory. Information processed by later parts of the dorsal stream (the parietal lobe) never reaches working memory and hence does not correlate with phenomenal awareness. I conclude that both blindsight and vision for action are genuinely unconscious visual processes.     

Pavlovian conditioning and rule learning

The experiment reviewed here was an attempt to show that two differential Pavlovian conditioning designs, namely positive and negative patterning, can best be understood as rule learning. First, it is shown that positive patterning is equivalent to the logical rule of conjunction (AND) and that negative patterning is equivalent to the logical rule of exclusive disjunction (XOR). It is assumed that in order to learn both kinds of discrimination subjects learn to use the according rule. If this is the case, the observed differentiation should be independent of the number of reinforcements for each individual stimulus. Second, subjects should be able to transfer the rule to new stimuli. Forty human subjects were randomly divided into four groups (N=10 each). Two factors were manipulated independently between subjects: (1) positive vs negative patterning, and (2) 2 vs 4 pairs of trained stimuli. Second interval skin conductance responses were measured. During initial acquisition positive as well as negative patterning occurred independently of number of pairs of trained stimuli (with total amount of training kept constant). Furthermore, AND as well as XOR could be transfered to new stimuli.     

The cognitive and neural correlates of "tactile consciousness": a multisensory perspective

People's awareness of tactile stimuli has been investigated in far less detail than their awareness of stimuli in other sensory modalities. In an attempt to fill this gap, we provide an overview of studies that are pertinent to the topic of tactile consciousness. We discuss the results of research that has investigated phenomena such as "change blindness", phantom limb sensations, and numerosity judgments in tactile perception, together with the results obtained from the study of patients affected by deficits that can adversely affect tactile perception such as neglect, extinction, and numbsense. The similarities as well as some of the important differences that have emerged when visual and tactile conscious information processing have been compared using similar experimental procedures are highlighted. We suggest that conscious information processing in the tactile modality cannot be separated completely from the more general processing of spatial information in the brain. Finally, the importance of considering tactile consciousness within the larger framework of multisensory information processing is also discussed.     

Matching- and nonmatching-to-sample concept learning in rats using olfactory stimuli

Previous research has shown that rats can learn matching-to-sample relations with olfactory stimuli; however, the specific characteristics of this relational control are unclear. In Experiment 1, 6 rats were trained to either match or nonmatch to sample in a modified operant chamber using common household spices as olfactory stimuli. After matching or nonmatching training with 10 exemplars, the contingencies were reversed with five new stimuli such that subjects trained on matching were shifted to nonmatching and vice versa. Following these reversed contingencies, the effects of the original training persisted for many trials with new exemplars. In Experiment 2, 9 rats were trained with matching procedures in an arena that provided for 18 different spatial locations for comparison stimuli. Five subjects were trained with differential reinforcement outcomes and 4 with only one type of reinforcer. Differential outcomes and multiple exemplars facilitated learning, and there was strong evidence for generalization to new stimuli for most rats that acquired several conditional discriminations. Performances with novel samples were generally above chance, but rarely reached the high levels obtained during baseline with well-trained stimulus relations. However, taken together, the data from the two experiments extend previous work, show that rats can learn both match and nonmatch relations with different experimental protocols, and demonstrate generalization to novel sample stimuli.