Dėmesio mirksėjimo efektas – tai plačiai žinomas reiškinys dėmesio tyrimuose. Jis atspindi dėmesingo informacijos apdorojimo ribas, kadangi greitai (10 stimulų per sekundę dažniu) toje pačioje regos lauko vietoje pateikus stimulų seką dažniausiai žmonės nepastebi ir/ arba neatsimena antrojo reikšminio stimulo. Tai įvyksta tuo atveju, kai šis pasirodo 200-500 ms intervale nuo pirmojo reikšminio stimulo pateikimo. Neseniai Martens ir kolegos (2006) nustatė, jog kai kuriems žmonėms dėmesio mirksėjimo efektas nepasireiškia, jie buvo pavadinti „nemirksinčiais“. Manoma, kad individualius skirtumus lemia nevienodai efektyvus gebėjimas iš nereikšmingos informacijos srauto išsirinkti reikšmingą. Šiame darbe siekta patikrinti, ar individuali darbinės atminties talpa, tiriamojo emocinė būsena ir tiriamojo asmenybės bruožai turi įtakos dėmesio efekto išreikštumui. Naudojant parametrizuotą dėmesio mirksėjimo efekto analizės būdą, nustatyta, kad didesnė darbinės atminties talpa sąlygoja mažesnį dėmesio mirksėjimo efektą. Šie rezultatai patvirtina nuomonę, kad dėmesio mirksėjimo efektas yra darbinės atminties talpos ribotumo pasekmė. Taip pat nustatyta, kad tiriamojo emocinio sužadinamumo būsena yra susijusi su dėmesio mirksėjimo efekto stiprumu, o asmenybės bruožai – su trukme. / The attentional blink is a well-known phenomenon in the study of attention. It reflects the impaired ability to identify the second of two targets presented in a rapid serial visual presentation (RSVP) of events if it appears between 200 and 500 ms after the first target. Recently Martens et al. (2006) reported that about 5% of the population (referred to as “non-blinkers”) shows little or no attentional blink under conditions in which most people (“blinkers”) do show. It is proposed that aforementioned differences are determined by individual differences in efficiency of ignoring irrelevant information. Thus, the aims of this master’s thesis were to investigate the impact of working memory capacity, emotional state and personality traits on attentional blink effect. Using parameterized attentional blink analysis method, based on curve fitting, the negative correlation between the size of attentional blink and working memory capacity was revealed. These findings support the idea that individual processing limitations and working memory play a key role in attentional blink. Also it was demonstrated that emotional arousal has impact on the strength of attentional blink and personality traits have effect on the span of attentional blink.

This paper provides evidence to support the hypothesis that the locus coeruleus – norephinephrine (LC-NE) system is the neurophysiological basis of both the attentional blink (AB) and the event related potential (ERP) component known as the P300. The LC-NE system is thought to provide a brief burst of processing facilitation in response to motivationally salient events. The AB refers to decreased accuracy for reporting the second of two targets (T1 and T2) inserted into a rapid serial visual presentation (RSVP). The LC-NE account of the AB holds that the AB is the result of a refractory-like period in LC-NE activity. The LC-NE account of the P300 suggests the P300 is the electrophysiological manifestation of the activity of the LC-NE system. I support the three-way link between these different aspects of brain activity by predicting differences in the AB dependent on characteristics of the P300 in response to T1 (T1-P300).

This paper provides evidence to support the hypothesis that the locus coeruleus – norephinephrine (LC-NE) system is the neurophysiological basis of both the attentional blink (AB) and the event related potential (ERP) component known as the P300. The LC-NE system is thought to provide a brief burst of processing facilitation in response to motivationally salient events. The AB refers to decreased accuracy for reporting the second of two targets (T1 and T2) inserted into a rapid serial visual presentation (RSVP). The LC-NE account of the AB holds that the AB is the result of a refractory-like period in LC-NE activity. The LC-NE account of the P300 suggests the P300 is the electrophysiological manifestation of the activity of the LC-NE system. I support the three-way link between these different aspects of brain activity by predicting differences in the AB dependent on characteristics of the P300 in response to T1 (T1-P300).

abstract: Magicians are informal cognitive scientists who regularly test their hypotheses in the real world. As such, they can provide scientists with novel hypotheses for formal psychological research as well as a real-world context in which to study them. One domain where magic can directly inform science is the deployment of attention in time and across modalities. Both magicians and scientists have an incomplete understanding of how attention operates in time, rather than in space. However, magicians have highlighted a set of variables that can create moments of visual attentional suppression, which they call "off-beats," and these variables can speak to modern models of temporal attention. The current research examines two of these variables under conditions ranging from artificial laboratory tasks to the (almost) natural viewing of magic tricks. Across three experiments, I show that the detection of subtle dot probes in a noisy visual display and pieces of sleight of hand in magic tricks can be influenced by the seemingly irrelevant rhythmic qualities of auditory stimuli (cross-modal attentional entrainment) and processes of working memory updating (akin to the attentional blink). / Dissertation/Thesis / Ph.D. Psychology 2013

The master´s thesis deals with fatigue evaluation in electrooculography records (EOG). The theoretical part focuses on electrooculography itself, fatigue and methods used for fatigue detection from EOG. The practical part includes a plan of optimal methodology for fatigue evaluation using EOG. The EOG signals are recorded during the volunteers are watching prepared scenes. Those scenes are desribed here. There is also definition of signal processing methods with relevant block diagrams. Laboratory protocol describing EOG signals recording using Biopac data acquisition system is included. Ten volunteers were measured according to this protocol and the signal database was created. In brief questionnaire volunteers were supposed to evaluate fatigue and discomfort of the measurment. Recorded signals were processed and acquired parameters were statistically evaluated. Then the parameters were discussed in terms of fatigue detection ability. On the basis of that software application was created. This application detects fatigue in selected signal. The thesis includes detailed laboratory manual for students.

abstract: A literature search revealed that previous research on the Attentional Blink (AB) has not examined the role of salience in AB results. I examined how salience affects the AB through multiple forms and degrees of salience in target 1 (T1) and target 2 (T2) stimuli. When examining increased size as a form of salience, results showed a more salient T2 increased recall, attenuating the AB. A more salient T1 did not differ from the control, suggesting the salience (increased size) of T2 is an important factor in the AB, while salience (increased size) of T1 does not affect the AB. Additionally, the differences in target size (50% or 100% larger) were not significantly different, showing size differences at these intervals do not affect AB results. To further explore the lack of difference in results when T1 is larger in size, I examined dynamic stimuli used as T1. T1 stimuli were presented as looming or receding. When T1 was presented as looming or receding, the AB was attenuated (T2 recall at lag 2 was significantly greater). Additionally, T2 recall was significantly worse at lags three and four (showing a larger decrease directly following the attenuated AB). When comparing looming and receding against each other, at lag 2 (when recall accuracy at its lowest) looming increased recall significantly more than receding stimuli. This is expected to be due to the immediate attentional needs related to looming stimuli. Overall, the results showed T2 salience in the form of size significantly increases recall accuracy while T1 size salience does not affect the AB results. With that, dynamic T1 stimuli increase recall accuracy at early lags (lag 2) while it decreases recall accuracy at later lags (lags 3 and 4). This result is found when the stimuli are presented at a larger size (stimuli appearing closer), suggesting the more eminent need for attention results in greater effects on the AB. / Dissertation/Thesis / Doctoral Dissertation Human Systems Engineering 2019

The thesis deals with eye blink detection, which is part of complex topic of face detection and recognition. The work intents on digital image processing. There is analyse of the topic and description of image databases for testing. Two main chapters describe design of eye blink detection with digital image processing with IR technology and without IR technology.

BACKGROUND.One group of theories aiming at providing a framework explaining the etiology, maintenance and phenomenology of anxiety disorders is classified as cognitive models of anxiety. These approaches assume that distortions in specific levels of information processing are relevant for the onset and maintenance of the disorder. A detailed knowledge about the nature of these distortions would have important implications for the therapy of anxiety, as the implementation of confrontative or cognitive elements precisely fitting the distortions might enhance efficacy. Still, these models and related empirical evidence provide conflicting assumptions about the nature of disorder-linked processing distortions. Many cognitive models of anxiety (e.g., Fox, Russo, & Dutton, 2002; Mathews & Mackintosh, 1998; Williams, Watts, MacLeod, & Mathews, 1997) postulate that anxiety-linked biases of attention imply hypervigilance to threat and distractibility from other stimuli in the presence of feared materials. This is convincingly confirmed by various experimentalclinical studies assessing attention for threat in anxious participants compared to non-anxious controls (for a review, seeMathews &MacLeod, 2005). In contrast, assumptions concerning anxiety-linked biased memory for threat are less convincing; based on the shared tendency for avoidance of deeper elaboration in anxiety disorders, some models predict memory biases only for implicit memory tasks (Williams et al., 1997) or even disclaim the relevance of memory in anxiety at all (e.g., Mogg, Bradley, Miles, & Dixon, 2004). Other theories restrict the possibility of measuring disorder-specific memory biases to tasks that require merely perceptual encoding of the materials instead of verbal-conceptual memory (e.g., Fox et al., 2002; Mathews &Mackintosh, 1998). On the one hand, none of these models has integrated all the inconsistencies in empirical data on the topic. On the other hand, the numerous empirical studies on memory in anxiety that have been conducted with varying materials, anxiety disorders, encoding and retrieval conditions do not allow final conclusions about the prerequisites for finding memory biases (for a review, see MacLeod & Mathews, 2004). A more detailed investigation of the complete spectrum of memory for threat utilizing carefully controlled variations of depth of encoding and materials is needed. In view of these inconsistencies, it is all the more surprising that one important part of this spectrum has so far remained completely uninvestigated: visual working memory (VWM). No study has ever differentially addressed VWM for threat in anxious vs. nonanxious participants and none of the cognitive models of anxiety provides any predictions concerning this stage of information processing. Research on cognitive biases in anxiety has thus far only addressed the two extremes of the processing continuum: attention and longer-term memory. In between, a gap remains, the bridging of which might bring us closer to defining the prerequisites of memory biases in anxiety. As empirical research has provided substantial and coherent knowledge concerning attention in anxiety, and as attention and VWM are so closely linked (see, for instance, Cowan, 1995), the thorough investigation of VWM may provide important clues for models of anxiety. Is anxiety related to VWM biases favoring the processing of threatening information, or does the avoidance presumed by cognitive models of anxiety already begin at this stage? RESEARCH AIMS. To investigate the relevance of biased VWM in anxiety, the present research focused in eight experiments on the following main research questions: (1) Is threat preferably stored in VWM in anxious individuals? (2) Does threat preference occur at the cost of the storage of other items, or is extra storage capacity provided? (3) Would the appearance of threat interrupt ongoing encoding of non-threatening items? (4) Does prioritized encoding of threat in anxiety occur strategically or automatically? (5) Are disorder-specific VWM biases also materials-specific? (6) Are VWM biases in anxiety modifiable through cognitive-behavioral therapy? METHODS. In Experiments 1-4, a spatial-sequential cueing paradigm was used. A subset of real-object display items was successively cued on each trial by a sudden change of the picture background for 150 ms each. After the cueing, one of the display pictures was hidden and probed for a memory test. On most trials, a cued item was tested, and memory accuracy was determined depending on the item’s position within the cue string and depending on its valence. In some cases, memory for an uncued item was tested. Experiment 1 and 2 were directed at discovering whether spider fearfuls and non-anxious controls would differ with respect to the accuracy in memorizing cued spiders and uncued spiders and, thus, reveal disorder-specific biases of VWM. In addition, the question whether the presence of a spider image is related to costs for the memorization of other images was tested. Experiment 3 addressed whether any disorder-specific VWM biases found earlier were specific to the feared spiders. Therefore, the critical stimuli here were a snake and a spider. Participants were spider fearfuls and non-anxious controls, both without snake anxiety. In Experiment 4, it was tested whether disorder-specific biases found in Experiment 1 and 2 were modifiable through cognitive-behavioral treatment. The critical stimulus was a spider image. Spider fearfuls were tested three times. Half of them received a cognitive-behavioral intervention after the first test, the other half only after the second test. In two additional experiments, VWM was assessed with a change-detection paradigm. The main aim was to clarify whether disorder-specific effects found in the previous experiments were associated with automatic or with strategic selective encoding of threatening materials, and whether any group differences in spider change detection were materials-specific to spiders, but not to snakes. In Experiment 5, several images were presented simultaneously in a study display for either 100 or 500 milliseconds. After a short interruption, a test display was presented including either the same items as the first one or one changed item. Participants’ accuracy in determining whether displays were the same or different was measured depending on the valence of the changed item, set size, and presentation time of the display. There were trials with and without spiders. If a change was made, it could involve either a non-spider or a spider item. Of specific interest was the condition in which a spider image was presented initially, but not in the test phase, as noticing this specific change would require storage of that image in VWM. Would group differences be particularly pronounced in the shorter encoding condition suggesting automatic encoding of threat, or would they occur in the longer encoding condition, suggesting strategic encoding of spiders? In Experiment 6, change detection accuracy for spiders vs. snakes was tested. The participants in both experiments were spider fearfuls vs. controls, but those of Experiment 6 were additionally required to lack snake anxiety. Moreover, a temporal VWM paradigm - an attentional blink task - was applied to assess whether a biased encoding of spider images in spider fearfuls would occur at the expense of non-threatening items undergoing concurrent processing, and whether this effect was specific to spiders, but not to snakes. Series of real-object pictures were presented at rates of 80 ms at the display center. The observer’s task was to identify and report the two target pictures indicated by a brighter background. In Experiment 7, the first target always depicted a neutral item. The valence of the second target was varied - either negative depicting a spider, positive, or neutral. Participants varied with respect to their spider anxiety. In Experiment 8, spider fearfuls and non-anxious controls, both without snake anxiety, were tested. The experiment was nearly the same as the previous one, but two negative target types were tested: disorder-relevant spiders and negative but not feared snakes. Of specific interest was whether the appearance of a threatening target would reduce the report probability of the earlier attended target, indicating the interruption of its VWM encoding in favor of the threat item. RESULTS. (1) Both anxious and non-anxious controls, showed VWM advantages for negative materials such as spider or snake images. (2) In addition, there were disorderspecific VWM biases: some effects were larger in spider fearfuls than in non-anxious controls and some effects occurred exclusively in spider fearfuls. (3) Group differences and, thus, disorder-specificity were particularly pronounced under competitive circumstances, that is, under the condition of numerous stimuli competing for processing resources: when only little orientation time was allowed, when only little time was provided for selecting and encoding items from a crowd, and when VWMfor the critical item required reflexive instead of voluntary attention. (4) Pronounced memory for task-relevant, voluntarily attended spiders was related to difficulties in disengaging attention from these items in the fearful group, reflected in reduced memory accuracy for the item following it. (5) Disorder-specific VWM biases seem to be based on attentional biases to threatening materials resulting in a very quick, automatic memory consolidation. However, this preferential encoding was not at the cost of neutral materials currently undergoing encoding processes. (6) All disorder-specific VWM biases occured only with fear-related materials, not with other negative materials. (7) Automatic and highly disorder-specific fear-related VWM biases – but not strategic VWM biases occuring in both groups - were modifiable through cognitive-behavioral intervention. CONCLUSIONS. This work provides additional information about informationprocessing distortions related to specific anxiety. With the experimental investigation of biased VWM, this work has been performed to fill a gap within research on cognitive biases in anxiety. Moreover, this dissertation contributes to cognitive theories of anxiety by proposing several recommendations for refinements of current theoretical approaches. Most important, it was suggested to extend existing models by a more detailed consideration of attention and memory. In view of numerous previous empirical studies on the topic and the conclusions of this dissertation, a differentiation of the attentional engagement and disengagement component appears inevitable. Even more important, in view of the data presented here predictions concerning VWM for threatening materials need to be taken into account. In addition, suggestions are provided for the differential consideration of biases occuring from prepotent threat value of negative stimuli vs. individual threat value. A proposal for a cognitive model of anxiety extended by all these aspects is provided to serve as an invitation of further research in the investigation of the nature of memory biases in anxiety disorders. REFERENCES: Cowan, N. (1995). Attention and Memory. An integrated framework.New York: Oxford University Press. Fox, E., Russo, R., & Dutton, K. (2002). Attentional bias for threat: Evidence for delayed disengagement from emotional faces. Cognition and Emotion, 16, 355-379. MacLeod, C., & Mathews, A. (2004). Selective memory effects in anxiety disorders: An overview of research findings and their implications. In D. Reisberg & P. Hertel (eds.), Memory and Emotion. Oxford: Oxford University Press. Mathews, A., & Mackintosh, B. (1998). A cognitive model of selective processing in anxiety. Cognitive Therapy and Research, 22 (6), 539-560. Mathews, A., & MacLeod, C. (2005). Cognitive vulnerability to emotional disorders. Annual Review of Clinical Psychology, 1, 167-195.Mathews, Mogg, May, & Eysenck (1989). Mogg, K., Bradley, B.P., Miles, F., & Dixon, R. (2004). Time course of attentional bias for threat scenes: Testing the vigilance avoidance hypothesis. Cognition and Emotion, 18(5), 689-700. Williams, J.M.G., Watts, F.N., MacLeod, C., & Mathews, A. (1997). Cognitive psychology and emotional disorders. Chichester: John Wiley.

Σκοπός της παρούσας Διπλωματικής Εργασίας είναι η ανάπτυξη και εφαρμογή τεχνικών ψηφιακής επεξεργασίας εικόνων για τον εντοπισμό του οφθαλμού και τον υπολογισμό συγκεκριμένων παραμέτρων που συνδέονται με την κατάσταση του χρήστη. Συγκεκριμένα, χρησιμοποιήθηκε ένα ολοκληρωμένο Σύστημα Εντοπισμού Οφθαλμού που περιλαμβάνει τα υποσυστήματα της CMOS κάμερα, της μεταφοράς δεδομένων – εικόνων, της ψηφιοποίησης των δεδομένων, και τέλος το υποσύστημα της επεξεργασίας εικόνων οφθαλμού και του υπολογισμού παραμέτρων. Στα πλαίσια του τελευταίου αυτού υποσυστήματος αναπτύχθηκαν δύο μεθοδολογίες που βασίστηκαν στην εφαρμογή αλγορίθμων ψηφιακής επεξεργασίας εικόνων. Η πρώτη μεθοδολογία βασίστηκε στον υπολογισμό της μέσης φωτεινότητας για την άνω και την κάτω περιοχή του οφθαλμού. Η χρονική μεταβολή των δύο τιμών της φωτεινότητας χρησιμοποιήθηκε για την εξαγωγή πληροφοριών για την κατάσταση του οφθαλμού (ανοιχτός ή κλειστός). Η δεύτερη μεθοδολογία στηρίχτηκε σε ένα συνδυασμό τεχνικών ψηφιακής επεξεργασίας εικόνων. Η επεξεργασία κάθε εικόνας της ακολουθίας video περιλαμβάνει τέσσερα βασικά βήματα: (α) ευθυγράμμιση της εικόνας σε σχέση με ένα κοινό σύστημα αναφοράς, (β) εφαρμογή δύο φίλτρων για την ανίχνευση των κορυφών και των κοιλάδων της εικόνας, (γ) σύντηξη των δύο φιλτραρισμένων εικόνων που προκύπτουν και (δ) μετατροπή της εικόνας σύντηξης σε δυαδική με εφαρμογή κατάλληλου κατωφλίου. Η καταμέτρηση των λευκών εικονοστοιχείων της δυαδικής εικόνας στην περιοχή του οφθαλμού καθορίζει την κατάσταση του οφθαλμού (ανοικτός ή κλειστός). Τέλος, και μέσω του λογισμικού, υπολογίζονται οι σχετικές παράμετροι της κατάστασης του οφθαλμού όπως ο αριθμός ανοιγο-κλεισίματος οφθαλμού, η διάρκεια κάθε ανοιγο-κλεισίματος οφθαλμού και οι χρονικές αποστάσεις μεταξύ των προσδιορισμένων ανοιγο-κλεισιμάτων σε μια αλληλουχία συλλεγμένων εικόνων. / The scope of the thesis was the development and application of digital image processing techniques in order to detect human eye in video sequences and determine parameters related to the user’s state. Specifically, an integrated Eye-Tracking System was used in order to obtain the necessary image frames for further processing. The System consists of four modules, the CMOS camera module, the transfer module, the digitization module and the software module. The software module was based on the application of image processing techniques to detect the eye and calculate specific parameters. Two image processing techniques were developed and tested throughout this thesis. The first method was based on the calculations of the mean brightness of the upper and lower eye region for each frame of the video sequence. The temporal variation of this mean value provided useful information for the eye state (open/closed). The second method was based on a combination of various image processing techniques. The processing of each video frame comprises of four basic steps: a) registration of the image in relation to the first frame of the video sequence, b) filtering in order to detect the peaks and valleys of the image being processed, c) fusion of the filtered images, and d) binarization of the fused image by thresholding. The calculation of the number of white pixels in the eye region of the binary image indicates the state of the eye (open/closed) and allows the determination of the blink parameters related to the user’s state (vigilance/somnolence). The parameters being measured throughout this thesis were the number of eye blinks, the blink duration and the blink interval.

BACKGROUND.One group of theories aiming at providing a framework explaining the etiology, maintenance and phenomenology of anxiety disorders is classified as cognitive models of anxiety. These approaches assume that distortions in specific levels of information processing are relevant for the onset and maintenance of the disorder. A detailed knowledge about the nature of these distortions would have important implications for the therapy of anxiety, as the implementation of confrontative or cognitive elements precisely fitting the distortions might enhance efficacy. Still, these models and related empirical evidence provide conflicting assumptions about the nature of disorder-linked processing distortions. Many cognitive models of anxiety (e.g., Fox, Russo, & Dutton, 2002; Mathews & Mackintosh, 1998; Williams, Watts, MacLeod, & Mathews, 1997) postulate that anxiety-linked biases of attention imply hypervigilance to threat and distractibility from other stimuli in the presence of feared materials. This is convincingly confirmed by various experimentalclinical studies assessing attention for threat in anxious participants compared to non-anxious controls (for a review, seeMathews &MacLeod, 2005). In contrast, assumptions concerning anxiety-linked biased memory for threat are less convincing; based on the shared tendency for avoidance of deeper elaboration in anxiety disorders, some models predict memory biases only for implicit memory tasks (Williams et al., 1997) or even disclaim the relevance of memory in anxiety at all (e.g., Mogg, Bradley, Miles, & Dixon, 2004). Other theories restrict the possibility of measuring disorder-specific memory biases to tasks that require merely perceptual encoding of the materials instead of verbal-conceptual memory (e.g., Fox et al., 2002; Mathews &Mackintosh, 1998). On the one hand, none of these models has integrated all the inconsistencies in empirical data on the topic. On the other hand, the numerous empirical studies on memory in anxiety that have been conducted with varying materials, anxiety disorders, encoding and retrieval conditions do not allow final conclusions about the prerequisites for finding memory biases (for a review, see MacLeod & Mathews, 2004). A more detailed investigation of the complete spectrum of memory for threat utilizing carefully controlled variations of depth of encoding and materials is needed. In view of these inconsistencies, it is all the more surprising that one important part of this spectrum has so far remained completely uninvestigated: visual working memory (VWM). No study has ever differentially addressed VWM for threat in anxious vs. nonanxious participants and none of the cognitive models of anxiety provides any predictions concerning this stage of information processing. Research on cognitive biases in anxiety has thus far only addressed the two extremes of the processing continuum: attention and longer-term memory. In between, a gap remains, the bridging of which might bring us closer to defining the prerequisites of memory biases in anxiety. As empirical research has provided substantial and coherent knowledge concerning attention in anxiety, and as attention and VWM are so closely linked (see, for instance, Cowan, 1995), the thorough investigation of VWM may provide important clues for models of anxiety. Is anxiety related to VWM biases favoring the processing of threatening information, or does the avoidance presumed by cognitive models of anxiety already begin at this stage? RESEARCH AIMS. To investigate the relevance of biased VWM in anxiety, the present research focused in eight experiments on the following main research questions: (1) Is threat preferably stored in VWM in anxious individuals? (2) Does threat preference occur at the cost of the storage of other items, or is extra storage capacity provided? (3) Would the appearance of threat interrupt ongoing encoding of non-threatening items? (4) Does prioritized encoding of threat in anxiety occur strategically or automatically? (5) Are disorder-specific VWM biases also materials-specific? (6) Are VWM biases in anxiety modifiable through cognitive-behavioral therapy? METHODS. In Experiments 1-4, a spatial-sequential cueing paradigm was used. A subset of real-object display items was successively cued on each trial by a sudden change of the picture background for 150 ms each. After the cueing, one of the display pictures was hidden and probed for a memory test. On most trials, a cued item was tested, and memory accuracy was determined depending on the item’s position within the cue string and depending on its valence. In some cases, memory for an uncued item was tested. Experiment 1 and 2 were directed at discovering whether spider fearfuls and non-anxious controls would differ with respect to the accuracy in memorizing cued spiders and uncued spiders and, thus, reveal disorder-specific biases of VWM. In addition, the question whether the presence of a spider image is related to costs for the memorization of other images was tested. Experiment 3 addressed whether any disorder-specific VWM biases found earlier were specific to the feared spiders. Therefore, the critical stimuli here were a snake and a spider. Participants were spider fearfuls and non-anxious controls, both without snake anxiety. In Experiment 4, it was tested whether disorder-specific biases found in Experiment 1 and 2 were modifiable through cognitive-behavioral treatment. The critical stimulus was a spider image. Spider fearfuls were tested three times. Half of them received a cognitive-behavioral intervention after the first test, the other half only after the second test. In two additional experiments, VWM was assessed with a change-detection paradigm. The main aim was to clarify whether disorder-specific effects found in the previous experiments were associated with automatic or with strategic selective encoding of threatening materials, and whether any group differences in spider change detection were materials-specific to spiders, but not to snakes. In Experiment 5, several images were presented simultaneously in a study display for either 100 or 500 milliseconds. After a short interruption, a test display was presented including either the same items as the first one or one changed item. Participants’ accuracy in determining whether displays were the same or different was measured depending on the valence of the changed item, set size, and presentation time of the display. There were trials with and without spiders. If a change was made, it could involve either a non-spider or a spider item. Of specific interest was the condition in which a spider image was presented initially, but not in the test phase, as noticing this specific change would require storage of that image in VWM. Would group differences be particularly pronounced in the shorter encoding condition suggesting automatic encoding of threat, or would they occur in the longer encoding condition, suggesting strategic encoding of spiders? In Experiment 6, change detection accuracy for spiders vs. snakes was tested. The participants in both experiments were spider fearfuls vs. controls, but those of Experiment 6 were additionally required to lack snake anxiety. Moreover, a temporal VWM paradigm - an attentional blink task - was applied to assess whether a biased encoding of spider images in spider fearfuls would occur at the expense of non-threatening items undergoing concurrent processing, and whether this effect was specific to spiders, but not to snakes. Series of real-object pictures were presented at rates of 80 ms at the display center. The observer’s task was to identify and report the two target pictures indicated by a brighter background. In Experiment 7, the first target always depicted a neutral item. The valence of the second target was varied - either negative depicting a spider, positive, or neutral. Participants varied with respect to their spider anxiety. In Experiment 8, spider fearfuls and non-anxious controls, both without snake anxiety, were tested. The experiment was nearly the same as the previous one, but two negative target types were tested: disorder-relevant spiders and negative but not feared snakes. Of specific interest was whether the appearance of a threatening target would reduce the report probability of the earlier attended target, indicating the interruption of its VWM encoding in favor of the threat item. RESULTS. (1) Both anxious and non-anxious controls, showed VWM advantages for negative materials such as spider or snake images. (2) In addition, there were disorderspecific VWM biases: some effects were larger in spider fearfuls than in non-anxious controls and some effects occurred exclusively in spider fearfuls. (3) Group differences and, thus, disorder-specificity were particularly pronounced under competitive circumstances, that is, under the condition of numerous stimuli competing for processing resources: when only little orientation time was allowed, when only little time was provided for selecting and encoding items from a crowd, and when VWMfor the critical item required reflexive instead of voluntary attention. (4) Pronounced memory for task-relevant, voluntarily attended spiders was related to difficulties in disengaging attention from these items in the fearful group, reflected in reduced memory accuracy for the item following it. (5) Disorder-specific VWM biases seem to be based on attentional biases to threatening materials resulting in a very quick, automatic memory consolidation. However, this preferential encoding was not at the cost of neutral materials currently undergoing encoding processes. (6) All disorder-specific VWM biases occured only with fear-related materials, not with other negative materials. (7) Automatic and highly disorder-specific fear-related VWM biases – but not strategic VWM biases occuring in both groups - were modifiable through cognitive-behavioral intervention. CONCLUSIONS. This work provides additional information about informationprocessing distortions related to specific anxiety. With the experimental investigation of biased VWM, this work has been performed to fill a gap within research on cognitive biases in anxiety. Moreover, this dissertation contributes to cognitive theories of anxiety by proposing several recommendations for refinements of current theoretical approaches. Most important, it was suggested to extend existing models by a more detailed consideration of attention and memory. In view of numerous previous empirical studies on the topic and the conclusions of this dissertation, a differentiation of the attentional engagement and disengagement component appears inevitable. Even more important, in view of the data presented here predictions concerning VWM for threatening materials need to be taken into account. In addition, suggestions are provided for the differential consideration of biases occuring from prepotent threat value of negative stimuli vs. individual threat value. 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