Skip to main content Accessibility help
×
Hostname: page-component-8448b6f56d-c4f8m Total loading time: 0 Render date: 2024-04-19T21:51:37.085Z Has data issue: false hasContentIssue false

5 - Temporal lobe – neocortical structures

Published online by Cambridge University Press:  25 August 2009

David L. Clark
Affiliation:
Ohio State University
Nashaat N. Boutros
Affiliation:
Yale University, Connecticut
Mario F. Mendez
Affiliation:
University of California, Los Angeles
Get access

Summary

Emil Kraepelin (1919) suggested that abnormalities in the frontal lobe were responsible for problems in reasoning and that damage to the temporal lobe resulted in delusions and hallucinations in patients with dementia praecox (schizophrenia). The classical findings of Kluver and Bucy in the 1930s clearly and strongly linked the temporal lobes to behavior. Their work provided the basis from which the concept of the limbic system has developed.

The temporal lobe can be divided into two regions: lateral and ventromedial. The lateral region supports cognitive functions associated with several sensory systems. It is recognized as neocortex and is the focus of this chapter. The ventromedial region of the temporal lobe contains major portions of the limbic system and thus contributes significantly to emotional tone. The ventromedial, limbic temporal lobe is discussed in Chapter 11.

It is now accepted that dysfunction of the dorsolateral region of the temporal lobe may be associated with several psychopathological states. Temporal lobe lesions due to a variety of neurological insults can lead a patient to present with signs and symptoms that are more consistent with a psychiatric diagnosis than with a traditional neurological one.

Anatomy and behavioral considerations

The temporal lobe lies ventral to the lateral fissure (of Sylvius) and the parietal lobe. It is rostral to the occipital lobe (Figure 5.1). The superior temporal sulcus and the lateral fissure lie above the superior temporal gyrus and are particularly deep.

Type
Chapter
Information
The Brain and Behavior
An Introduction to Behavioral Neuroanatomy
, pp. 53 - 69
Publisher: Cambridge University Press
Print publication year: 2005

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Andreasen, N. C., O'Leary, D. S., Arndt, S., Cizadlo, T., Hurtig, R., Rezai, K., Watkins, G. L., Ponto, L. B., and Hichwa, R. D. 1996. Neural substrates of facial recognition. J. Neuropsychiatry Clin. Neurosci. 8: 139–146.Google ScholarPubMed
Augustine, J. R. 1996. Circuitry and functional aspects of the insular lobe in primates including humans: a full-length review. Brain Res. Brain Res. Rev. 22:229–244.CrossRefGoogle Scholar
Barta, P. E., Pearlson, G. D., Powers, R. E., Richards, S. S., and Tune, L. E. 1990. Auditory hallucinations and smaller superior temporal gyral volume in schizophrenia. Am. J. Psychiatry 147:1457–1462.Google Scholar
Blair, R. J., Frith, U., Smith, N., Abell, F., and Cipolotti, L. 2002. Fractionation of visual memory: agency detection and its impairment in autism. Neuropsychologia 40:108–118.CrossRefGoogle ScholarPubMed
Blakemore, S.-J., and Decety, J. 2001. From the perception of action to the understanding of intention. Nature Rev. Neurosci. 2:561–567.Google ScholarPubMed
Borod, J. C., Martin, C. C., Alpert, M., Brozgold, A., and Welkowitz, J. 1993. Perception of facial emotion in schizophrenic and right brain-damaged patients. J. Nerv. Ment. Dis. 181:494–502.CrossRefGoogle ScholarPubMed
Bruder, G., Rabinowicz, E., Towey, J., Brown, A., Kaufmann, C. A., Amador, X., Malaspina, D., and Gorman, J. M. 1995. Smaller right ear (left hemisphere) advantage for dichotic fused words in patients with schizophrenia. Am. J. Psychiatry 152:932–935.Google ScholarPubMed
Brunswick, N., McCrory, E., Price, C., Frith, C. D., and Frith, U. 1999. Explicit and implicit processing of words and pseudowords by adult developmental dyslexics: a search for Wernicke's Wortschatz?Brain 122:1901–1917.CrossRefGoogle ScholarPubMed
Bryson, G., Bell, M., Kaplan, E., Greig, T., and Lysaker, P. 1998. Affect recognition in deficit syndrome schizophrenia. Psychiatry Res. 77:113–120.CrossRefGoogle ScholarPubMed
Büchel, C., Price, C. J., and Friston, K. J. 1998. A multimodal language area in the ventral visual pathway. Nature 394:274– 277.CrossRefGoogle ScholarPubMed
Carmichael, S. T., and Price, J. L. 1995. Limbic connections of the orbital and medial prefrontal cortex in macaque monkeys. J. Comp. Neurol. 363:615–641.CrossRefGoogle ScholarPubMed
Cipolotti, L., Robinson, G., Blair, J., and Frith, U. 1999. Fractionation of visual memory: evidence from a case with multiple neurodevelopmental impairments. Neuropsychologia 37:329–332.CrossRefGoogle ScholarPubMed
Cleghorn, J. M., Franco, S., Szechtman, B., Kaplan, R. D., Szechtman, H., Brown, G. M., Nhmias, C., and Garnett, E. S. 1992. Toward a brain map of auditory hallucinations. Am. J. Psychiatry 149:1062–1069.Google Scholar
Cox, D., Meyers, E., and Sinha, P. 2004. Contextually evoked object-specific responses in human visual cortex. Science 304:115–117.CrossRefGoogle ScholarPubMed
Critchley, H. D., Wiens, S., Rothshtein, P., Ohman, A., and Dolan, R. J. 2004. Neural systems supporting interoceptive awareness. Nature Neurosci. 7(2): 189–195.CrossRefGoogle ScholarPubMed
Crow, T. J. 1997. Schizophrenia as failure of hemispheric dominance for language. Trends Neurosci. 20:339–343.Google ScholarPubMed
Cutting, J. 1994. Evidence for right hemisphere dysfunction in schizophrenia. In: David, A. S. and Cutting, J. C. (eds.) The Neuropsychology of Schizophrenia. Hove, England: Erlbaum, pp. 321–242.Google ScholarPubMed
Drake, M. E. 1987. Postictal Capgras syndrome. Clin. Neurol. Neurosurg. 89:4CrossRefGoogle ScholarPubMed
Fried, I. 1997. Auras and experiential responses arising in the temporal lobe. J. Neuropsychiatry. Clin. Neurosci. 9:420–428.Google ScholarPubMed
Geschwind, N. 1965. Disconnexion syndromes in animals and man. Brain 88:269–272.CrossRefGoogle ScholarPubMed
Gloor, P. 1997. The Temporal Lobe and Limbic System. New York: Oxford University Press.Google Scholar
Goldsmith, S. K., Shapiro, R. M., and Joyce, J. N. 1997. Disrupted pattern of D2 dopamine receptors in the temporal lobe in schizophrenia. Arch. Gen. Psychiatry 54:649–658.CrossRefGoogle Scholar
Hasson, U., Nir, Y., Levy, I., Fuhrmann, G., and Rafael, M. 2004. Intersubject synchronization of cortical activity during natural vision. Science 303(5664):1634–1640.CrossRefGoogle ScholarPubMed
Haxby, J. V., Gobbini, M. I., Furey, M. L., Ishai, A., Schouten, J. L., and Pietrini, P. 2001. Distributed and overlapping representations of faces and objects in ventral temporal cortex. Science 293(5539):2425–2430.CrossRefGoogle ScholarPubMed
Heining, M., Young, A. W., Ioannou, G., Andrew, C. M., Brammer, M. J., Gray, J. A., and Phillips, M. L. 2003. Disgusting smells activate human anterior insula and ventral striatum. Ann. N. Y. Acad. Sci. 1000:380–384.CrossRefGoogle ScholarPubMed
Kanwisher, N., McDermott, J., and Chun, M. M. 1997. The fusiform face area: a module in human extrastriate cortex specialized for face perception. J. Neurosci. 17(11):4302–4311.CrossRefGoogle ScholarPubMed
Keshavan, M. S., David, A. S., Steingard, S., and Lishman, W. A. 1992. Musical hallucinations: a review and synthesis. Neuropsychiatry Neuropsychol. Behav. Neurol. 5:211–223.Google Scholar
Ketter, T. A., Andreason, P. J., George, M. S., Lee, C., Gill, D. S., Parekh, P. I., Willis, M. W., Herscovitch, P., and Post, R. M. 1996. Anterior paralimbic mediation of procaine-induced emotional and psychosensory experiences. Arch. Gen. Psychiatry 53:59–69.CrossRefGoogle ScholarPubMed
Kircher, T. T. J., Brammer, M. J., Levelt, W., Bartels, M., and McGuire, P. K. 2004. Pausing for thought: engagement of the left temporal cortex during pauses in speech. Neuroimage 21:84–90.CrossRefGoogle Scholar
Kraepelin, E. 1919/1971. Dementia Praecox. Barclay, E., and Barclay, S. (trans.). New York: Churchill Livingstone.Google Scholar
Kringelbach, M. L., Araujo, I. E. T., and Rolls, E. T. 2004. Taste-related activity in the human dorsolateral prefrontal cortex. Neuroimage 21:781–788.CrossRefGoogle ScholarPubMed
Kulynych, J. J., Vladar, K., Jones, D. W., and Weinberger, D. R. 1994. Gender differences in the normal lateralization of the supratemporal cortex: MRI surface-rendering morphometry of Heschl's gyrus and the planum temporale. Cereb. Cortex 4:107–118.CrossRefGoogle ScholarPubMed
Kwon, J. S., McCarley, R. W., Hirayasu, Y., Anderson, J. E., Fischer, I. A., Kikinis, R., Jolesz, F. A., and Shenton, M. E. 1999. Left planum temporale volume reduction in schizophrenia. Arch. Gen. Psychiatry 56:142–148.CrossRefGoogle Scholar
Lane, R., Reiman, E. M., Ahern, G. L., Schwartz, G. E., and Davidson, R. J. 1997. Neuroanatomical correlates of happiness, sadness, and disgust. Am. J. Psychiatry 154:926–933.Google ScholarPubMed
Lawrie, S. M., Buechel, C., Whalley, H. C., Frith, C. D., Friston, K. J., and Johnstone, E. C. 2002. Reduced frontotemporal functional connectivity in schizophrenia associated with auditory hallucinations. Biol. Psychiatry 51:1008–1011.CrossRefGoogle ScholarPubMed
Lehmann, C., Mueller, T., Federspiel, A., Hubl, D., Schroth, G., Huber, O., Strik, W., and Dierks, T. 2004. Dissociation between overt and unconscious face processing in fusiform face area. Neuroimage 21:75–83.CrossRefGoogle ScholarPubMed
Levin, H., and Kraus, M. F. 1994. The frontal lobes and traumatic brain injury. J. Neuropsychiatry Clin. Neurosci. 6:443–454.Google ScholarPubMed
Malloy, P., Cimino, C., and Westlake, R. 1992. Differential diagnosis of primary and secondary Capgras delusions. Neuropsychiatry Neuropsychol. Behav. Neurol. 5:83–96.Google Scholar
Mann, C. A., Lubar, J. R., Zimmerman, A. W., Miller, C. A., and Muenchen, R. A. 1992. Quantitative analysis of EEG in boys with attention deficit hyperactivity disorder: controlled study with clinical implications. Pediatr. Neurol. 8:20–36.CrossRefGoogle ScholarPubMed
McCarley, R. W., Shenton, M. E., O'Donnell, B. F., and Nestor, P. G. 1993a. Uniting Kraepelin and Bleuler: the psychology of schizophrenia and the biology of temporal lobe abnormalities. Harv. Rev. Psychiatry 1:36–56.CrossRefGoogle Scholar
McCarley, R. W., Shenton, M. E., O'Donnell, B. F., Gaux, S. F., Kikinis, R., Nestor, G., and Jolesz, F. A. 1993b. Auditory 300 abnormalities and left superior temporal gyrus volume reduction in schizophrenia. Arch. Gen. Psychiatry 50:190–197.CrossRefGoogle Scholar
Mega, M. S., Cummings, J. L., Salloway, S., and Malloy, P. 1997. The limbic system: an anatomic, phylogenetic, and clinical perspective. J. Neuropsychiatry Clin. Neurosci. 9:315–330.Google ScholarPubMed
Mendez, M. F. 2001. Generalized auditory agnosia with spared music recognition in a left-hander. Analysis of a case with a right temporal stroke. Cortex 37:139–150.CrossRefGoogle Scholar
Mendez, M. F., and Cummings, J. L. 2003. Dementia: A Clinical Approach, 3rd edn. New York: Butterworth-Heineman, p. 206.Google Scholar
Moran, M. Z., Mufson, E. J., and Mesulam, M. M. 1987. Neural inputs into the temporopolar cortex of the rhesus monkey. J. Comp. Neurol. 256:88–103.CrossRefGoogle ScholarPubMed
Narumoto, J., Ikada, T., Sadato, N., Fukui, K., and Yonekura, Y. 2001. Attention to modulate fMRI activity in human right superior temporal sulcus. Brain Res. Cogn. Brain Res. 12:225–231.CrossRefGoogle Scholar
O'Donnell, B. F., Faux, S. F., McCarley, R. W., Kimble, M. O., Salisbury, D. F., Nestor, P. G., Kikinis, R., Jolesz, F. A., and Shenton, M. E. 1995. Increased rate of P300 latency prolongation with age in schizophrenia. Arch. Gen. Psychiatry 52:544–549.CrossRefGoogle Scholar
Ogawa, H. 1994. Gustatory cortex of primates: anatomy and physiology. Neurosci. Res. 20:1–13.CrossRefGoogle ScholarPubMed
Oppenheimer, S. 1993. The anatomy and physiology of cortical mechanisms of cardiac control. Stroke 24(Suppl. 12):I3–I5.Google ScholarPubMed
Pandya, D. N., Rosene, D. L., and Doolittle, A. M. 1994. Corticothalamic connections of auditory-related areas of the temporal lobe in the rhesus monkey. J. Comp. Neurol. 345(3):447–471.CrossRefGoogle ScholarPubMed
Paulesu, E., Frith, C. D., and Frackowiak, R. S. J. 1993. The neural correlates of the verbal component of working memory. Nature 362:342–344.CrossRefGoogle ScholarPubMed
Petty, R. G., Barta, P. E., Pearlson, G. D., McGilchrist, I. K., Lewis, R. W., Tien, A. Y., Pulver, A., Vaughn, D. D., Casanova, M. F., and Powers, R. E. 1995. Reversal of asymmetry of the planum temporale in schizophrenia. Am. J. Psychiatry 152(5):715–721.Google Scholar
Potkin, S. G., Alva, G., Fleming, K., Anand, R., Keator, D., Carreon, D., Doo, M., Jin, Y., Wu, J. C., and Fallon, J. H. 2002. A PET study of the pathophysiology of negative symptoms in schizophrenia. Positron emission tomography. Am. J. Psychiatry 159(2):227–237.CrossRefGoogle ScholarPubMed
Reiman, E. M. 1997. The application of positron emission tomography to the study of normal and pathologic emotions. J. Clin. Psychiatry 58(Suppl. 16):4–12.Google Scholar
Reiman, E. M., Raichle, M. E., Robins, E., Mintun, M. A., Fusselman, M. J., Fox, P. T., Price, J. L., and Hackman, K. A. 1989. Neuroanatomical correlates of a lactate-induced anxiety attack. Arch. Gen. Psychiatry 46:493–500.CrossRefGoogle ScholarPubMed
Reiman, E. M., Lane, R. D., Ahern, G. L., Schwartz, G. E., Davidson, R. J., Friston, K. J., Yun, L.-S., and Chen, K. 1997. Neuroanatomical correlates of externally and internally generated human emotion. Am. J. Psychiatry 154(7):918–925.Google ScholarPubMed
Reite, M., Sheeder, J., Teale, P., Adams, M., Richardson, D., Simon, J., Jones, R. H., and Rojas, D. C. 1997. Magnetic source imaging evidence of sex differences in cerebral lateralization in schizophrenia. Arch. Gen. Psychiatry 54:433–440.CrossRefGoogle Scholar
Roper, S. N., Levesque, M. F., Sutherling, W. W., and Engel, J. Jr. 1993. Surgical treatment of partial epilepsy arising from the insular cortex. J. Neurosurg. 79:266–269.CrossRefGoogle ScholarPubMed
Rubin, P., Karle, A., Moller-Madsen, S., Hertel, C., Povlsen, U. J., Noring, U., and Hemmingsen, R. 1993. Computerised tomography in newly diagnosed schizophrenia and schizophreniform disorder. A controlled blind study. Br. J. Psychiatry 163:604–612.CrossRefGoogle ScholarPubMed
Shenton, M. E., Kikinis, R., Jolesz, F. A., Pollack, S. D., LeMay, M., Wible, C. G., Hokama, H., Martin, J., Metcalf, D., Coleman, M., and McCarley, R. W. 1992. Abnormalities of the left temporal lobe and thought disorder in schizophrenia: a quantitative magnetic resonance imaging study. N. Engl. J. Med. 327:604–612.CrossRefGoogle ScholarPubMed
Shergill, S. S., Bullmore, E., Simmons, A., Murray, R., and McGuire, P. 2000. Functional anatomy of auditory verbal imagery in schizophrenic patients with auditory hallucinations. Am. J. Psychiatry 157:1691–1693.CrossRefGoogle ScholarPubMed
Small, D. M., Zald, D. H., Jones-Gotman, M., Zatorre, R. J., Pardo, J. V., Frey, S., and Petrides, M. 1999. Human cortical gustatory areas: a review of functional neuroimaging data. Neuroreport 10:7–14.CrossRefGoogle ScholarPubMed
Sno, H. N. 1994. A continuum of misidentification symptoms. Psychopathology 27:144–147.CrossRefGoogle ScholarPubMed
Southard, E. E. 1910. A study of the dementia praecox group in the light of certain cases showing anomalies or scleroses in particular brain regions. Am. J. Insanity 67:119–176.Google Scholar
Stoléru, S., Grégoire, M.-C., Gérard, D., Decety, J., Lafarge, E., Cinotti, L., Lavenne, F., LeBars, D., Vernet-Maury, E., Rada, H., Collet, C., Mazoyer, B., Forest, M. G., Magnin, F., Spira, A., and Comar, D. 1999. Neuroanatomical correlates of visually evoked sexual arousal in human males. Arch. Sex. Behav. 28(1):1–21.CrossRefGoogle ScholarPubMed
Suzuki, M., Yuasa, S., Minabe, Y., Murata, M., and Kurachi, M. 1993. Left superior temporal blood flow increases in schizophrenia and schizophreniform patients with auditory hallucination: a longitudinal case study using 123I-IMP SPECT. Eur. Arch. Psychiatry Clin. Neurosci. 242:257–261.CrossRefGoogle ScholarPubMed
Tabert, M. H., Borod, J. C., Tang, C. Y., Lange, G., Wei, T. C., Johnson, R., Nusbaum, A. O., and Buchsbaum, M. S. 2001. Differential amygdala activation during emotional decision and recognition memory tasks using unpleasant words: an fMRI study. Neuropsychologia 39:556–573.CrossRefGoogle ScholarPubMed
Tzourio-Mazoyer, N., Schonen, S. D., Crivello, F., Reutter, B., Aujard, Y., and Mazoyer, B. 2002. Neural correlates of woman face processing by 2-month-old infants. Neuroimage 15:454–461.CrossRefGoogle ScholarPubMed
Ungerleider, L. G., and Mishkin, M. 1982. Two cortical visual systems. In: Ingle, D. J., Goodale, M. H., and Mansfield, R. J. W. (eds.) The Analysis of Visual Behavior. Cambridge, Mass: M.I.T. Press.Google Scholar
Vuilleumier, P., Armong, J. L., Driver, J., and Dolan, R. J. 2001. Effects of attention and emotion of face processing in the human brain: an event-related fMRI study. Neuron 30(3):829–841.CrossRefGoogle Scholar
Wolberg, Z., and Newman, J. D. 1972. Auditory cortex of squirrel monkey: response patterns of single cells to species-specific vocalizations. Science 175:212–214.CrossRefGoogle Scholar
Young, M. W., Robinson, I. H., Hellavell, D. J., dePauw, K. E., and Pentland, B. 1992. Cotard delusion after brain injury (case study). Psychol. Med. 21:799–804.CrossRefGoogle Scholar

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×