Running head: MEANTAL ABILITY & SENSORY DISCRIMINATION Mental Ability and Sensory Discrimination _____________________________________ A Thesis Presented to St. Thomas University ____________________________________ In Partial Fulfillment of the Requirements for the Degree of Bachelor of Arts with Honours in Psychology ____________________________________ Alexandra Smith April 2012 1 MENTAL ABILITY & SENSORY DISCRIMINATION 2 Table of Contents Acknowledgements……………………………………………………………………...3 Abstract……………………………………………………………………………….....4 Introduction……………………………………………………………………………...5 Method………………………………………………………………………………….15 Results…………………………………………………………………………………...17 Discussion……………………………………………………………………………….19 References……………………………………………………………………………….23 MENTAL ABILITY & SENSORY DISCRIMINATION 3 Acknowledgements The past year has presented me with the opportunity of working with many people who have made the completion of my honours thesis possible. I would like to take this opportunity to thank them. First and foremost, I would like to thank my advisor, Dr. Michael Houlihan, for his continuous support and expertise. I would also like to thank my reader, Dr. Del Brodie, for his advice and helpful recommendations. To Dr. Kim Fenwick- thank you for your guidance throughout the year, that kept us all on track. Kris DesRoches, Ian Davidson, and Lauren Morrisey, I cannot express how much I appreciated your help with data collection. I would also like to thank all the other volunteers who provided their assistance in the lab. Finally, to all the participants who took the time to make this research possible. MENTAL ABILITY & SENSORY DISCRIMINATION 4 Abstract The study of intelligence has always been popular in the field of psychology. A rather recent approach in measuring cognitive abilities involves its assessment in the absence of attention. The aim of the present study examines the relationship between intelligence and auditory sensory discrimination abilities. Fluid intelligence represents an individual’s ability to comprehend and manipulate patterns, as well as to adapt to novel situations. Fluid intelligence, which is the most accurate predictor of general intelligence, was measured using the Advanced Matrices Test. Sensory discrimination was assessed using the mismatch negativity, an even-related potential (ERP) reflected in the EEG recording. This was recorded while the participants were presented with a series of sounds varying in intensity. The mismatch wave demonstrates one’s ability to discriminate between the sounds, without attending to them. The amplitude of the mismatch negativity has been found to predict sensory discrimination abilities and discrimination abilities are found to predict mental abilities. Thus the brain’s innate ability to discriminate between varying intensities of auditory paradigms at an unconscious level is hypothesized to predict mental abilities. MENTAL ABILITY & SENSORY DISCRIMINATION 5 Mental Ability & Sensory Discrimination Advancements in the study of intelligence contest sensory discrimination capabilities are an apposite index of mental abilities. Higher cognitive abilities are congruent with better sensory discrimination accuracy. The understanding of mental abilities and their assessment is highly valuable, as intelligence tests are determined the most accurate indication of academic and career achievement (Haavisto & Lehto, 2004). As cognitive abilities are frequently measured through fluid intelligence assessments, an overview of the encompassing three-stratum intelligence model will be discussed. Further, a review of the biological determinants of fluid intelligence and the psychometric measurement of sensory discrimination through the ERP is in order. Frequency but not duration discrimination accurately correlate with mental abilities (Troche, Houlihan, Stelmack, & Rammsayer, 2010). Thus, the aim of this research seeks to identify the parameters of sensory discrimination as a predictor of intelligence through the manipulation of auditory intensity. Fluid and Crystallized Intelligence A descriptive model of intelligence that has been researched over the past 100 years, is the model of general intelligence, as proposed by Spearman in 1904. Through factor analysis, Spearman (1904) outlined specific cognitive tasks and specialized abilities correlated with the concept of general intelligence (Haavisto & Lehto, 2004). These specialized abilities that are predictive of general intelligence include skills such as visual perception, spatial reasoning and nonverbal capabilities (Haavisto & Lehto, 2004), however these abilities do not all share the same correlations with general intelligence. A positive manifold effect is observed within the three stratum hierarchy, as all cognitive abilities correlated with the construct of general intelligence; several predictors more accurately anticipate general intelligence than do others MENTAL ABILITY & SENSORY DISCRIMINATION 6 (van der Maas et al., 2006). These abilities are measured through intelligence batteries, and are organized in a hierarchical model, where general intelligence was the highest order strata. The second stratum consists of the specific cognitive abilities, and the tests used to assess these abilities consist of the first stratum. Cattell and Horn contest that the third stratum of general intelligence does not fully encompass all cognitive loadings; rather fluid and crystallized intelligence better served this model. The Cattell-Horn-Carroll (CHC) model, however, is generally the most accepted model of intelligence by all within the field, which encompasses the ideas of Spearman’s general intelligence as the highest order of intelligence (McGrew, 2009). Fluid and crystallized intelligence are both original subsets of general intelligence, as proposed by Cattell (1963). Both are described as second-order functions of general intelligence in the CHC model. Fluid intelligence is the ability to easily adapt to novel environments, and to create inferences, thus it is the ability think fluidly. Crystal intelligence involves the use of previously acquired information and skills. Fluid skills, however, are not dependant on the acquisition of facts, rather reliant upon an individual’s ability to think abstractly. Preusse et al. (2011) suggest greater fluid intelligence is the proficiency of integrating previous knowledge and applying it to the present. Tasks exercising fluid intelligence require cognitive processing in a manner to create inferences to solve in a novel situation (Kan et al., 2011). Fluid capabilities involve the recognition and comprehension of patterns (Preusse et al., 2011). Further, competency in mathematics is reported in high fluid capabilities (Preusse et al., 2011) and fluid intelligence is the most accurate indicator of general intelligence (Wooglar et al., 2010). Crystallized intelligence requires the use of previous knowledge for comprehension, whereas previously acquired knowledge is not imperative in exercising fluid intelligence. MENTAL ABILITY & SENSORY DISCRIMINATION 7 Crystallized intelligence is culturally based, often reflecting school curriculums among young children (Cattell 1963). Further, crystallized intelligence is dependant on fluid intelligence, as Kan et al. (2011) report individuals with high fluid intelligence abilities acquire higher levels of crystallized intelligence. In time limited cognitive tasks, fluid intelligence is of greater advantage than crystallized (Cattell, 1963), this is because fluid intelligence is the ability to create inferences and adapt to novel situations, and the use previously acquired information is not necessary. However, individuals dominant in crystallized intelligence better perform in tasks where time is not limited, and the task involves knowledge such as history or geography, where they are able to apply their existing knowledge to complete a task successfully (Cattell, 1963). Biology of Mental Ability Biological models that complement the factor analysis framework of intelligence purport mental ability is in large due to neurons and specific areas of the brain. Galton (1883) proposed intellect was a product of an individual’s ability to discriminate (as cited in Meyer, Hagmannvon Arx, Lemola, & Grob, 2010). Jenson’s (1982) neural oscillation theory predicts mental abilities are determined by the conductance speed of neurons. Thus processing information at a greater speed is indicative of higher cognitive abilities (as cited in Helmbold, Troche, & Rammsayer, 2006). Current research maintains these theoretical views, and expand on the neural oscillation models. For example, the degree of myelination of the neurons is proposed to play a crucial role in intelligence (Jung & Haier, 2007). Jung and Haier (2007) purport myelin density affects the size of the axon, and consequently the large axon size will increase the conduction speed of neural impulses. Individuals whom process information more quickly because of this neural efficiency are considered to have higher cognitive abilities (Jung & Haier, 2007). Additionally, white matter was positively correlated with intelligence, which further reinforces MENTAL ABILITY & SENSORY DISCRIMINATION 8 the myelination findings from previous work (Jung & Haier, 2009; Jung & Haier, 2007). White matter of the brain consists of myelinated neurons that are indicative of the speed of neural processing. Therefore, the degree of white matter found in the brain makes is consistent with the myelination of neurons. Jung and Haier (2007) propose exercising cognitive abilities activates the parietal and frontal areas of the brain, known as the parietal frontal integration theory (PFIT). Therefore, the PFIT model indicates intelligence results from the interaction between these neural structures, rather than centralized in one unique area (Preusse et al., 2011). Sensory information is processed initially in the occipital and auditory cortexes, for visual and acoustic stimuli, respectively (Preusse, van deer Meer, Deshpande, Krueger, & Wartenbuger, 2011). The encoded information is then sent from the parietal to the frontal cortex for interpretation. Cognitive processes exercising fluid capabilities are reported to activate the parietal and frontal lobes of the brain (Preusse et al., 2011). This demonstrates cognitive processes activate several neural pathways, and intellect results from the integration of multiple cortices (Preusse et al., 2011). Colom et al. (2009) investigated fluid, crystallized and spatial intelligence and it’s relationship with the PFIT model previously proposed (Jung & Haier, 2007). Specific areas of the brain are active when general, crystallized and spatial intelligence are exercised, however no significant area was determined for fluid intelligence. This suggests fluid intelligence is an activation of multiple cortical areas. The frontal and parietal cortices are implicated with fluid intelligence, as when completing a matrices task that requires fluid thinking, activation of these areas, as measured by increase blood flow was observed (Kane & Engle, 2002). The EEG and Event-Related Potential MENTAL ABILITY & SENSORY DISCRIMINATION 9 The electroencephalogram (EEG) is a functional research technique that allows for the recording of differences in neural electrical activity (Coles & Rugg, 1995). This is achieved in placing electrode sensors on the scalp (Coles & Rugg, 1995). In a research paradigm, stimuli sequences are presented, and variations in the voltage of the EEG are observed respective to each stimulus. This measure of cortical differences in voltage is recorded from the onset of a stimulus to it’s neural processing, and therefore is time-locked to the neural processing of the stimuli. Averaging is used to extract the event-related potential (ERP), and it is representative of the neural processing of the stimuli (Coles & Rugg, 1995). Thus, the ERP is representative of the processing of information (the stimuli) over a particular time period. Once the ERP is derived from the EEG raw data, the amplitude and latency may be measured (Coles & Rugg, 1995). The amplitude refers to the strength of the ERP, or how positive or negative the wave is at it’s peak. Latency measures the time elapsed from stimulus onset to the processing of the event (Coles & Rugg, 1995). The ERP is useful in many research paradigms, including ones of memory and discrimination (Duncan et al., 2009). The Mismatch Negativity Waveform An oddball paradigm is the most reliable auditory sequence used when eliciting the mismatch negativity waveform. This involves a sequence of standard and deviant tones, where the deviant tones occur 20% of the time to violate a pattern created by the sequence of standard ones. The deviant tones may differ in parameters such as pitch, frequency, and intensity (Duncan et al., 2009). Pakarinen et al. (2010) reveal these standard tones do not need to be identical, however may follow an abstract rule in which the mismatch will nonetheless be elicited. An example of an abstract rule may consist of the standard tone following a pattern of increasing degrees of intensity, therefore each standard tone differs from the previous, yet is not considered MENTAL ABILITY & SENSORY DISCRIMINATION 10 deviant as it follows the rules of the pattern (Paavilainen, Simola, Jaramillo, Naatanen, & Winkler, 2003). Theses stimuli are presented while attention is directed elsewhere, an unrelated task is completed, which stimulates a separate sensory system. Therefore, the mismatch negativity is elicited in the absence of attention and represents the innate ability to detect change among stimuli. The mismatch negativity is derived from subtracting the standard from the deviant ERP waveform (Pakarinen, Huotainen, & Naatanen, 2010). The mismatch negativity is identified as the portion of the subtracted waveform between 150 and 250 ms after the onset of stimuli (Pakarinen et al., 2010) and is largest at the frontal electrode sites, however is also distinct at the site of the auditory cortex (Duncan et al., 2009; Naatanen 1990). The amplitude of the mismatch negativity waveform increases and shorter latencies are observed when the standard and deviant tones are more easily distinguished (Naatanen, 2008). Therefore, the accuracy in discriminating between the standard and deviant tones is positively correlated with larger amplitudes (Naatanen, 2008). Reduced amplitude is demonstrated when a tone is obscure in nature and consequently the amplitude of the mismatch negativity wave decreases as the degree of difficulty increases (Naatanen, 2008). The latency of the mismatch negativity wave is shorter when the difference between the frequent and deviant tone is largest. The amplitude of the waveform demonstrates a concentration of frontal activity (Duncan et al., 2009). This frontal activation reflects the attention switch in attending to the stimuli (Duncan et al., 2009). The mismatch negativity is elicited from several source generators including the auditory cortex, which in turn activates the frontal cortex (Naatanen, Tervaniemi, Sussman, Paavilainen, & Winkler, 2001). The frontal lobe is responsible for attending, thus it maintains where (to which stimulus) an individuals’ attention is held (Naatanen et al., 2011). The activation of the MENTAL ABILITY & SENSORY DISCRIMINATION 11 frontal cortex represents an individual’s shift in attention processing. However, the auditory cortex must first process the acoustic information in order for the switch in cortical activation to occur. The auditory cortex is responsible for categorizing all auditory stimulation; it must differentiate between all streams unique in pitch, length, and tone, and coins each stream to its’ original source. Naatanen et al. (2001) termed this “auditory stream segregation” (p. 283), where the auditory cortex functions to differentiate and organize all incoming acoustic streams, thus creating an afferent model of the stimuli. This entire process occurs at an attention-independent level. The mismatch negativity is elicited once the auditory cortex recognizes one sound stream is split into two (Naatanen et al., 2001). Thus, the auditory cortex compares each stream automatically, and when a tone infringes the past representation, the mismatch negativity is elicited. Further, the mismatch negativity is elicited when the expectation of the proceeding auditory event is not met; rather the sequence deviated from the norm (Naatanen et al., 2001). The expectation of the standard pattern is formed as a sensory memory trace in the auditory cortex. The auditory cortex compares each tone to this trace, and therefore distinguishes the deviant tone, as it violates the pattern held in echoic memory. The strength of this memory trace is reflected in the amplitude of the waveform (Bazana & Stelmack, 2002). This further demonstrates the auditory cortex’s ability to maintain several auditory streams in memory simultaneously and the sensitivity of the mismatch negativity, in the brains’ ability to discriminate when the standard is more obscure (Naatanen et al., 2001; Naatanen, Astikainen, Ruusuvirta, Huotilainen, 2010). The elicitation of the mismatch negativity through abstract standard paradigms represents the processing of the auditory stimuli occurs at a pre-attentive level and is contested to be a measure of intelligence (Naatanen et al., 2001). Further, it is MENTAL ABILITY & SENSORY DISCRIMINATION 12 suggested that the auditory cortex is able to keep more permanent streams of auditory information in memory. This is reflected through the use of language (Naatanen et al., 2001) and is vital for the recognition of speech violations. The mismatch negativity is an appropriate measure of discrimination as this waveform is elicited in the absence of attention (Duncan et al., 2009). As the mismatch negativity is elicited while attention is directed elsewhere, this demonstrates the sensory discrimination of the unattended auditory stimuli occurs at an attention-independent level. Therefore, direct attention is not needed to detect the differences of acoustic parameters. The detection of discrimination in auditory stimuli has been elicited during REM sleep, while in a coma, in newborns and even in fetuses (Nataanen, Kujala, & Winkler, 2011; Naatanen, Astikainen, Ruusuvirta, & Huotilainerf, 2010). Mismatch Negativity and Cognitive Abilities The mismatch negativity amplitude has been found to be predictive of mental abilities in multiple reports. A relationship between response time and cognitive ability is demonstrated in the report from Bazana and Stelmack (2002), where higher cognitive ability individuals completed a cognitive task, more accurately and in less time than did lower ability individuals. Mismatch negativity waves were elicited in a backward masking auditory oddball paradigm. The inter-tone interval (ITI), the duration between the standard or deviant tone and the mask, was manipulated. Shorter ITI were presumed to have a higher degree of difficulty, and therefore, smaller mismatch negativity amplitudes and longer latencies would be reflected in the results, as well as decreased accuracy among both high and low cognitive ability groups. Shorter response times and mismatch negativity latencies were found. However, the manipulation of the ITI displayed no significant effects for accuracy neither in discrimination, nor in the mismatch MENTAL ABILITY & SENSORY DISCRIMINATION 13 negativity amplitudes. Therefore, Bazana & Stelmack (2002) postulate the ITI did not interfere with the memory trace of the paradigm, perhaps because the masking stimulus was compounded with the standard or deviant tone, and thus perceived as a single unified tone. Shorter latencies, however, were reflected for the mismatch negativity higher ability group. These findings support the hypothesis of higher cognitive ability as a result of neural efficiency and speed (Beauchamp & Stelmack, 2006). ITI, frequency and type of the masking stimulus were manipulated in a subsequent report (Beauchamp & Stelmack, 2006). Consistent with the findings of Bazana and Stelmack (2002), shorter latencies were observed with shorter ITI. This contradicts the findings of Winkler and Naatanen (1999), who reported shorter ITI would increase the degree of difficulty and decrease accuracy in responses (as cited in Bazana and Stelmack, 2002). Shorter latencies of the mismatch negativity among higher ability individuals found, and demonstrate sensory discrimination and response speed is involved with cognitive abilities and intelligence. This is because shorter response times for higher ability individuals are prevalent across all conditions of the experimental paradigm (Beauchamp & Stelmack, 2006). The type of masking tone however does effect the elicitation of the mismatch negativity. The mask tones used by Beauchamp and Stelmack (2006) varied in degrees of difficulty and thus the elicitation of the mismatch negativity varied accordingly. The use of white noise as a masking tone is suggested to have a lower degree of difficulty because individuals are less likely to conceive this stimulus as compounded with the preceding standard or deviant tone. Therefore, participants displayed greater response accuracy and took less time to respond to the deviant to the target when the mask type used was white noise. In the masking paradigm however, higher ability participants MENTAL ABILITY & SENSORY DISCRIMINATION 14 demonstrated shorter latencies, reflecting their ability to process the stimuli more efficiently than lower-ability participants. In a recent report of frequency and duration discrimination, Troche et al. (2010) observed individuals of higher cognitive abilities displayed larger mismatch negativity amplitudes in an auditory frequency discrimination task. Further, high cognitive abilities predicted larger amplitudes in the mismatch negativity waveform across all conditions presented including frequency, duration and near-threshold parameters. High cognitive abilities however, were not indicative of discrimination abilities during the duration discrimination task. This may suggest the mismatch negativity is reflective of the ability to access sensory memory rather than discrimination ability as previous research has detailed (Troche et al., 2010). Because the mismatch negativity amplitude did not predict sensory discrimination accuracy, it is suggested the ability to access the memory trace of the auditory cortex that may be indicative of cognitive ability. This suggests higher ability individuals have an easier time detecting change among the parameters of the stimuli. The relationship between mental ability and sensory discrimination is supported in the recent findings of Houlihan and Stelmack (2012). Positive correlations between larger mismatch negativity amplitudes and mental ability scores were observed, in an auditory paradigm following an abstract rule. Mismatch negativity amplitudes are contested to be an index of sensory discrimination abilities. Previous reports have demonstrated sensory discrimination is predictive of mental abilities (Beauchamp & Stelmack, 2006; Troche et al., 2010; Houlihan & Stelmack, 2012). These findings are consistent with the theory of neural oscillation, as individuals of higher mental ability process information at a greater speed than those of low mental ability. It is expected MENTAL ABILITY & SENSORY DISCRIMINATION 15 larger mismatch negativity amplitudes and shorter latencies will be observed in high mental ability individuals. Method Participants Participants included female first year psychology, undergraduate students aged 18 to 24 (n= 47, m-18.6, SD=1.04). Data was eliminated from four participants due to poor signal to noise ratios . Since larger amplitudes are observed in females (Ikezawa et al., 2008) males were excluded from the sample. Only individuals with normal hearing were permitted to participate. Individuals administrating centrally acting medication or with neurological disorders were excluded from the study. The participants were required to abstain from consumption of alcohol 24 hours prior to their recording, and caffeine and nicotine one hour prior. Course credit and monetary remuneration were awarded to the participants for their contribution. Ethics approval was received from the St. Thomas Research Ethics Board. Measures The Adaptive Matrices Task test was designed using the Rasch dichotomous probabilistic test model and the standard measurement error is set at .63 for form S3 corresponding to a reliability of .87 (Hornke, Etzel, & Rettig, 2011) and provides the most precise estimate of general intelligence. The test is computer based, and adapts to the abilities of the participant. The format of this test is a 3 x 3 matrix, with a series of geometric patterns, where the bottom right cell of the matrix is missing. Eight options are given, and the participant was required to select the appropriate option that best fits the sequence presented. The test first presents a matrix of medium difficulty, and the proceeding items are of either increasing or decreasing difficulty until the participant gives an incorrect or correct response. The test stops once the participant answers MENTAL ABILITY & SENSORY DISCRIMINATION 16 10 successive questions either incorrectly or correctly, although this is not probable. The test will also stop if the participant has answered 30 matrices, which indicates the responses are not consistent and therefore a reliable measure cannot be given. Procedure The participant attended two data collection sessions. Participants initially performed the computer based Adaptive Matrices Task. This task was completed in a group setting. The participants were told to take their time when selecting their response, and were advised to spend at least one minute per question. Further, the participants were informed that if they responded too quickly to the questions, their score would not provide a reliable measure of their abilities. If this were the case, the participant would not be permitted to attend the second session. The subsequent session was scheduled to occur 1 to 30 days following the cognitive assessment. EEG data was recorded while the participant viewed a silent film with subtitles, and was concurrently presented with a series of auditory stimuli. The participant selected one of the following animated films to view: Toy Story 3, How to Train you Dragon, Monsters Inc., Shrek 2, Shrek 3, or Ice Age. The participants were instructed to ignore the auditory stimuli during the recording. Six sound sequences that followed an oddball sequence of standard and deviant sounds varying in intensity, each of which consisted of 680 standard tones and 120 deviant tones, were presented to each participant. In order to create a memory trace of the standard sound, the standard was presented 20 times at the beginning of each sequence. This was to ensure the elicitation of the mismatch negativity waveform, as this ERP component is measured at an attention independent level. The standard white noise sounds in all sequences were threshold, 2x threshold and 3x threshold in intensity, and 200 ms duration. This threshold was determined during a pilot study, MENTAL ABILITY & SENSORY DISCRIMINATION 17 with a 75dB standard. This was the minimal difference in intensity needed for the participant to articulate and decide which sound from a selection was loudest. The inter-tone-interval was 600 ms from onset to onset, with a10 ms rise and fall time. Electrophysiological recording The EEG was recorded using the EasyCap electrode cap using 32 Ag/AgCl electrodes, referenced to the nose, and AFz as the ground. Filter settings included Neuroscan NuAmp 0.5 to 100 Hz, with a sampling rate of 500Hz. In an offline analysis, vertical EOG was measured from one electrode placed below the right eye and FP2. Horizontal EOG was measured from F7 and F8. EOG was corrected using a regression-based algorithm provided by NeuroScan. The mismatch negativity wave was derived from the subtraction of the standard from the deviant ERP waveforms. Amplitude and latency was quantified as the point of maximal amplitude between 145 and 250 ms following onset. The data was visually reviewed for artifacts, filtered from 1 and 15Hz, and epoch averages were computed separately for each condition. ERP epochs were created between-50-400ms. Separate averages were calculated for standard and deviant tones in each condition, the mismatch negativity calculated as difference between standard and rare. Results The relationship between auditory intensity and mismatch amplitude and latency were evaluated using a mixed measures analysis of variance with a repeated measures factor of electrode locus and a between subjects factor of IQ group. High and low IQ groups were created based on median split of the Advanced Matrices test scores. No significant results were found at the level of p< .05 [F(3, 123) = 1.906, p >.05, = .720] for latency. Null effects were observed for the between subjects effects for IQ [F (1, 41) > 1, NS]. The interaction of locus and IQ group MENTAL ABILITY & SENSORY DISCRIMINATION 18 yielded no interaction [F (3, 123) = 1.974, p >.05, = .720]. P values were adjusted using Greenhouse Geisser corrections for the factor of locus. The relationships between cognitive ability and mismatch negativity amplitude, and cognitive ability and mismatch negativity latency, were calculated using Pearson’s r correlations. No correlations yielded significant results at p < .05 level (see table 1). Table 1 Amplitude r Mean Latency SD r Mean SD FZ .183 -.60 .632 .125 202.65 29.574 FC1 .086 -.67 .763 .125 201.21 28.838 FC2 .237 -.69 .767 .161 201.77 30.134 CZ .164 -.67 .891 .138 200.79 29.462 Figure 1 Grand Average MENTAL ABILITY & SENSORY DISCRIMINATION 19 Figure 1. The grand mismatch negativity averages for all conditions of threshold, twice threshold and thrice threshold. Discussion The present study examined the observed relationship between mental ability and auditory sensory discrimination, manipulating the intensity of auditory stimuli. Previous reports from Troche et al. (2010) and Houlihan & Stelmack (2012) found larger mismatch negativity amplitudes elicited during frequency discrimination and paradigms following an abstract deviance rule significantly correlated with cognitive ability scores. Thus the current study predicted individuals of high mental ability would demonstrate superior sensory discrimination facility, and consequently larger mismatch negativity amplitudes would be elicited. The findings however, did not support the hypothesis in the present analysis of auditory intensity manipulation, mismatch characteristics, and mental ability. There are several explanations for the inability to find a relation between mental ability and sensory discrimination. One possible conclusion from the lack of significant correlations with mental ability is that there is no relation between the processes represented by the mismatch negativity and intelligence. Previous research indicates frequency deviance in an oddball patterns, and sequences following an abstract rule elicit larger mismatch negativity amplitudes among higher cognitive ability individuals (Troche et al., 2010; Houlihan & Stelmack, 20120). No interaction effect, however, was found between mental ability and mismatch negativity amplitude or latency. Further, the correlations of mental ability scores and mismatch negativity amplitude scores yielded no significant findings. Therefore, future research is required to confirm whether intensity discrimination abilities may accurately predict mental abilities. MENTAL ABILITY & SENSORY DISCRIMINATION 20 The observed null effects may infer the parameters of discrimination abilities do not extend to intensity manipulation. The present mismatch negativity amplitude results, however, is inconsistent with previous findings from Schroger et al. (1996), Pakarinen et al. (2007), and Houlihan & Stelmack (2012), all of who reported significant results of larger mismatch negativity amplitudes through intensity manipulation, in oddball, optimal and abstract paradigms. This supports mismatch negativity amplitude as an reliable index of discrimination abilities at an attention-independent level. The mismatch negativity amplitudes observed in the present study are considerably smaller (less negative) relative to previous research (Troche et al., 2010). This lends evidence that the intensity deviance used did not elicit the intended mismatch negativity amplitudes. The intensity thresholds that were used in the study were calculated from pilot data that used a different computer and sound system. The differences in the two computer sound systems led to overall differences in intensity and therefore the intended discriminability of the stimuli may not have been achieved on the new computer. As the differences between the standard and deviant stimuli increase, that is—unconscious deviance detection increases in facility, larger mismatch negativity amplitudes are elicited (Naatanen et al., 2001). As the mismatch negativity amplitudes were uncommonly small, and this was observed in both high and low mental ability participants, suggests the intensity paradigm was entirely too difficult. Due to the hardware difficulties, the threshold levels presented to the participant were not as indicated, the differences were much smaller. Therefore, the null correlations reported may be caused by the poor, and unreliable elicitation of the mismatch negativity. Moreover, because the amplitudes of the mismatch negativity were so small, and therefore did not provide adequate measures of sensory discrimination, it is plausible intensity discrimination is predictive of mental abilities. Figure 2 MENTAL ABILITY & SENSORY DISCRIMINATION 21 provides an illustration of the current mismatch negativity amplitudes relative to the amplitudes observed in Troche et al. (2010) that yielded significant results. Future research is needed to confirm this hypothesis. Using ERP data to examine and predict mental abilities has proven beneficial and valuable to many facets in the discipline of psychology. The mismatch negativity allocates mental abilities to be measured without active attention, in a field dominated by intelligence batteries all of which require participant attention to complete. Although no support for the hypothesis of relation between mismatch negativity amplitude and intelligence was found, this may be due to the discriminability of the standard and deviant stimuli used rather than the lack of relation between the mismatch negativity and intelligence. Therefore, the current findings promote future research, replicating this paradigm with more appropriate stimuli, to examine the parameters of intelligence testing at an attention independent level. Figure 2 Mismatch Negativity Amplitudes Figure 2. Mismatch negativity amplitudes from current study and from previous findings of Troche et al. (2010), which yielded significant correlations with mental ability. The amplitudes MENTAL ABILITY & SENSORY DISCRIMINATION 22 from the current study are considerably smaller than previous findings, which may be due to the discriminability of standard and deviant stimuli used. MENTAL ABILITY & SENSORY DISCRIMINATION 23 References Bazana, P. G., & Stelmack, R. M. (2002). Intelligence and information processing during an auditory discrimination task with backward masking: An even-related potential analysis. Journal of Personality and Social Psychology, 83, 998-1008. Beauchamp, C. M., & Stelmack, R. M. (2006). The chronometry of mental ability: An eventrelated potential analysis of an auditory oddball discrimination task. Intelligence, 34, 571586. Colom, R., Haier, R. J., Head, K., Alvarez-Linera, J., Quiroga, M. A., Shih, P. C., & Jung, R. E. (2009). Gray matter correlates of fluid, crystallized, and spatial intelligence: Testing the P-FIT model. Intelligence, 37, 124-135. Conway, A. R. A., Cowan, N., Bunting, M. F., Therriault, D. J., & Minkoff, S. R. B. (2002). A latent variable analysis of working memory capacity, short-term memory capacity, processing speed, and general fluid intelligence. Intelligence, 30, 163-184. Duncan, C. C., Barry, R. J., Connolly, J. F., Fischer, C., Michie, P. T., Naatanen, R., Polich, J., Reivang, I., & Petten, C. V. (2009). Event-related potentials in clinical research: Guidelines for eliciting, recording, and quantifying mismatch negativity, P300, and N400. Clinical Neurophysiology, 120, 1883-1908. Helmbold, N., Troche, S., & Rammsayer, T. (2006). Temporal information processing and pitch discrimination as predictors of general intelligence. Canadian Journal of Experimental Psychology, 60, 294-306. Hornke, L. F., Etzel, S., & Rettig, K. (2011). Adaptive Matrices Test Manual. Schuhfried, Version 27. Modling, Austria. Houlihan, M. & Stelmack, R. M. (2012). Mental ability and mismatch negativity: Pre-attentive MENTAL ABILITY & SENSORY DISCRIMINATION 24 discrimination of abstract feature conjunctions in auditory sequences. Intelligence, 40, 239-244. Ikezawa, S., Nakagome, K., Mimura, M., Shinoda, J., Itoh, K., Homma, I., & Kamijima, K. (2008). Gender differences in lateralization of mismatch negativity in dichotic listening tasks. International Journal of Psychophysiology, 68, 41-50. Jung, R. E., & Haier, R. J. (2007). The parieto-frontal integration theory (P-FIT) of intelligence: Converging neuroimaging evidence. Behavioral and Brain Sciences, 30, 135-154. Kan, K-J., Kievit, R. A., Dolan, C., der Maas, H. v. (2011). On the interpretation of the CHC factor Gc. Intelligence, 39, 292-302. Kane, M. J. & Engle, R. W. (2002). The role of the prefrontal cortex in working-memory capacity, executive attention, and general fluid intelligence: An individual-differences perspective. Psychonomic Bulletin & Review, 9, 637-671. May, P. J. C., & Tiitinen, H. (2010). Mismatch negativity (MMN), the deviance-elicited auditory deflection, explained. Psychophysiology, 47, 66-122. McGrew, K., S. (2009). CHC theory and the human cognitive abilities project: Standing on the shoulders of the giant psychometric intelligence research. Intelligence, 37, 1-10. Meyer, C. S., Hagmann-von Arx, P., Lemola, S., & Grob, A. (2010). Correspondence between the general ability to discriminate sensory stimuli and general intelligence. Journal of Individual Differences, 31, 46-56. Naatanen, R. (1990). The role of attention in auditory information processing as revealed by event-related potentials and other brain measures of cognitive function. Behavioral and Brain Sciences, 13, 201-288. Naatanen, R., Astikainen, P., Ruusuvirta, T., & Huotilainerf, M. (2010). Automatic auditory MENTAL ABILITY & SENSORY DISCRIMINATION 25 intelligence: An expression of the sensory-cognitive core of cognitive process. Brain Research Reviews, 64, 123-136. Naatanen, R., Kujala, T., & Winkler, I. (2011). Auditory processing that leads to conscious perception: A unique window to central auditory processing opened by the mismatch negativity and related responses. Psychophysiology, 48, 4-22. Naatanen, R., Tervaniemi, M., Sussman, E., Paavilainen, P., & Winkler, I. (2001) ‘Primitive intteligence’ in the auditory cortex. TRENDS in Neurosciences, 24, 283-288. Naatanen, R. (2008). Mismatch negativity (MMN) as an index of central auditory system plasticity. International Journal of Audiology, 47, 16-20. Pakarinen S., Huotilainen, M., & Naatanen, R. (2010). The mismatch negativity (MMN) with no standard stimulus. Clinical Neurophsyiology, 121, 1043-1050. Paavilainen, P., Simola, J., Jaramillo, M., Naatanen, R., & Winkler, I. (2003). Preattentive extraction of abstract feature conjunctions from auditory stimulation as reflected by the mismatch negativity (MMN). Psychophysiology, 38, 359-365. Preusse, F., van der Meer, E., Deshpande, G., Krueger, F., & Wartenburger, I. (2011). Fluid intelligence allows flexible recruitment of the parieto-frontal network in analogical reasoning. Frontiers in Human Neuroscience, 5, 1-14. Rammsayer, T. H., & Brandler, S. (2002). On the relationship between general fluid intelligence and psychophysical temporal resolution in the brain. Journal of Research in Personality, 36, 507-530. Rugg, M. D., & Coles, M. G. H. (1995). Electrophysiology of mind: Event-related brain potentials and cognition. Oxford, England UK: Oxford University Press. Schroger, E., Tervaniemi, M., Wolff, C., & Naatenen, R. N. (1996). Preattentive periodicity MENTAL ABILITY & SENSORY DISCRIMINATION 26 detection in auditory patterns as governed by time and intensity information. Cognitive Brain Research, 4, 145-148. Spearman, C. (1904). “General intelligence”, Objectively determined and measured. The American Journal of Psychology, 15, 201-292. Tian, X., & Huber, D. E. (2008). Measures of spatial similarity and response magnitude in MEG and scalp EEG. Brain Topgor, 20, 131-141. Troche, S. J., Houlihan, M. E., Stelmack, R. M., & Rammsayer, T. H. (2010). Mental ability and the discrimination of auditory frequency and duration change without focused attention: An analysis of mismatch negativity. Personality and Individual Differences, 49, 228-233. Van der Maas, H. L. J, Dolan, C. V., Grasman, R. P. P. P., Wicherts, J. M., Huizenga, H. M., & Raijmakers, M. E. J. (2006). A dynamical model of general intelligence: The positive manifold of intelligence by mutualism. Psychology Review, 113, 842-861. Wooglar, A., Parr, A., Cusack, R., Thompson, R., Nimmo-Smith, I., Torralva, T., Roca, M., Antoun, N., Manes, F., & Duncan, J. (2010). PNAS Proceedings of the National Academy of Sciences of the United States of America, 107, 14899-14902.