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  • 1
    Publication Date: 2005-11-08
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bullock, Theodore H -- Bennett, Michael V L -- Johnston, Daniel -- Josephson, Robert -- Marder, Eve -- Fields, R Douglas -- New York, N.Y. -- Science. 2005 Nov 4;310(5749):791-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Scripps Institution of Oceanography and Department of Neuroscience, University of California, San Diego, La Jolla, CA 92093, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16272104" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials ; Animals ; Astrocytes/physiology ; Axons/physiology ; Brain/*physiology ; Cell Communication ; Dendrites/physiology ; Gap Junctions/physiology ; Humans ; *Nervous System Physiological Phenomena ; Neuroglia/physiology ; Neurons/cytology/*physiology ; Neurotransmitter Agents/physiology ; Synapses/physiology ; Synaptic Transmission
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1984-08-03
    Description: The brain has diversified and advanced in evolution more than any other organ; the variety of nervous systems and behaviors among animal species is thus available for our exploitation. Comparative neuroscience is likely to reach insights so novel as to constitute revolutions in understanding the structure, functions, ontogeny, and evolution of nervous systems. This promise requires pursuit on a wide front, in respect to disciplines and in respect to the species, stages, and states compared. It also requires deliberate concentration on the differences among animals, in addition to the prevailing concern for the basic and common. Neglect of these challenges would be costly. Without due consideration of the neural and behavioral correlates of differences between higher taxa and between closely related families, species, sexes, and stages, we cannot expect to understand our nervous systems or ourselves.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bullock, T H -- New York, N.Y. -- Science. 1984 Aug 3;225(4661):473-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6740319" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Evolution ; Brain/*physiology ; Electrophysiology ; Humans ; Invertebrates ; Neurons/physiology ; Species Specificity ; Synapses/physiology ; Vertebrates
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. Central processing of electroreceptor, mechanoreceptor, and optic input in rays (primarilyTorpedo) and sharks (primarilyScyliorhinus) was studied by recording evoked potentials to both direct nerve shock and natural physiological stimulation. We found that electrosensory input has a widespread, complex central representation; convergence of different modalities occurs in the midbrain, and rays show some consistent differences from sharks in response dynamics. 2. Each modality shows distinct forms of evoked potential with a different dependence on recording locus and depth, and a different sequence of recovery, facilitation and depression on stimulus repetition. 3. InTorpedo, unlike sharks, the trigeminal nerve is quite distinctly divided into electrosensory (ampullary receptors) and mechanosensory (cutaneous) branches; inputs from these major branches have clearly separable central distributions and dynamics, with evoked responses to direct shock of the maxillary branch showing similarities to, and interactions with responses to d.c. fields in the water. 4. Electrosensory and mechanosensory responses in both rays and sharks demonstrate integrative properties already in the medulla, and optic responses also demonstrate early integration, with much longer latencies, in the retina. Prominent, complex, long-lasting responses occur in the tectum bilaterally, but greater contralaterally, with each modality having a different locus of maximum responses. Responses to each modality also occur less prominently, often with different latencies or dynamics, in the telencephalon, cerebellum, and structures deep to the tectum. 5. The various rays were consistently different from the sharks in having slower responses to each modality, much slower following capability to repetitive stimuli, and in being extremely resistant to electroshock convulsion. We suggest that the physiological differences in central sensory responses between these rays and sharks may be relevant in analyzing their different behavior.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 79 (1972), S. 15-27 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. Potamotrygon lacks ampullae of Lorenzini (defined by their long canals), otherwise general for elasmobranchs. There are present however microscopic ampullary organs with extremely short canals. A brief histologic description is provided, together with counts of their abundance in various parts of the body. They are chiefly concentrated ventrally in the head region. 2. The skin has a relatively high resistance compared to marine rays. This is measured in the physiologically significant way, by measuring the potential distribution in and around a living ray placed in a homogenous electric field. 3. The microscopical size of the ampullary organs and the high skin resistance are believed to be a specialization maintaining the electroreceptive function in the low conductivity, fresh water medium. 4. These rays are shown to be responsive to d.c. and low-frequency a.c. electric fields. They give specific movements seemingly related to feeding. They seem to be less sensitive than marine sharks and rays. The threshold stimulus is probably less than 120 μV/cm (corresponding to 0.03 μA/cm2 with water resistivity of 4 kOhm · cm). 5. Potamotrygon circularis appears to lack Savi's vesicles. However, an organ which may be equivalent is a tubular, subcutaneous, receptor in the Submandibular region. It does not open to the outside or connect to the skin or to the skeleton. Its spontaneous background nerve impulses and the increases in firing with mechanical stimuli are described.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Neuroscience 5 (1982), S. 121-170 
    ISSN: 0147-006X
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Physiology 13 (1951), S. 261-280 
    ISSN: 0066-4278
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Medicine , Biology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Neuroscience 16 (1993), S. 1-16 
    ISSN: 0147-006X
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 519 (1987), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 164 (1989), S. 459-474 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The physiology of mechanoreceptive lateral line areas was investigated in the thornback guitarfish,Platyrhinoidis triseriata, from medulla to telencephalon, using averaged evoked potentials (AEPs) and unit responses as windows to brain functions. Responses were analysed with respect to frequency sensitivity, intensity functions, influence of stimulus repetition rate, response latency, receptive field (RF) organization and multimodal interaction. 1. Following a quasi-natural vibrating sphere stimulus, neural responses were recorded in the medullary medial octavolateralis nucleus (MON), the dorsal (DMN) and anterior (AN) nucleus of the mesencephalic nuclear complex, the diencephalic lateral tuberal nucleus (LTN), and a telencephalic area which may correspond to the medial pallium (Figs. 2, 3, 13, 14, 15, 16). 2. Within the test range of 6.5–200 Hz all lateral line areas investigated responded to minute water vibrations. Best frequencies (in terms of displacement) were between 75 and 200 Hz with threshold values for AEPs as low as 0.005 μm peak-to-peak (p-p) water displacement calculated at the skin surface (Fig. 6). 3. AEP-responses to a vibrating sphere stimulus recorded in the MON are tonic or phasic-tonic, i.e., responses are strongest at stimulus onset but last for the whole stimulus duration in form of a frequency following response (Fig. 3). DMN and AN responses are phasic or phasic-tonic. Units recorded in the MON are phase coupled to the stimulus, those recorded in the DMN, AN or LTN are usually not (Figs. 5, 8, 9). Diencephalic LTN and telencephalic lateral line responses (AEPs) often are purely phasic. However, in the diencephalic LTN tonic and/or off-responses can be recorded (Fig. 11). 4. For the frequencies 25, 50, and 100 Hz, the dynamic intensity range of lateral line areas varies from 12.8 to at least 91.6 dB (AEP) respectively 8.9 and 92 dB (few unit and single unit recordings) (Fig. 7). 5. Mesencephalic, diencephalic, and telencephalic RFs, based on the evaluation of AEPs or multiunit activity (MUA), are usually contralateral (AN and LTN) or ipsi- and contralateral (telencephalon) and often complex (Figs. 10, 12, 16). 6. In many cases no obvious interactions between different modalities (vibrating sphere, electric field stimulus, and/or a light flash) were seen. However, some recording sites in the mesencephalic AN and the diencephalic LTN showed bimodal interactions in that an electric field stimulus decreased or increased the amplitude of a lateral line response and vice versa (Fig. 13B).
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 168 (1991), S. 247-257 
    ISSN: 1432-1351
    Keywords: Epidermal lines ; Lateral line ; Mechanoreception ; Cephalopods ; Sepia officinalis ; Microphon-ic potential
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Potentials were recorded from the epidermal head lines and from the CNS of young cuttlefish, Sepia officinalis, in response to weak water movements. 1. Within the test range 0.5–400 Hz a sinusoidal water movement elicits up to 4 components of response if the electrode is placed on a headline: (i) a positive phasic ON response; (ii) a tonic frequency-following microphonic response; (iii) a slow negative OFF response (Figs. 2, 5, 7A, 8, 11); and (iv) compound nerve impulses (Figs. 3A, 7B). 2. The amplitude of both the ON wave and the microphonic potential depends on stimulus frequency, stimulus amplitude and stimulus rise time (Figs. 4C, 6). Frequencies around 100 Hz and short rise times are most effective in eliciting strong potentials. The minimal threshold was 0.06 μm peak-to-peak water displacement at 100 Hz (18.8 μm/s as velocity). 3. Change of direction of tangential sphere movement (parallel vs. across the head lines) has only a small effect on the microphonic and the summed nerve potentials (Fig. 7). 4. Frequency and/or amplitude modulations of a carrier stimulus elicit responses at the onset and offset of the modulation and marked changes in the tonic microphonic response (Figs. 8, 9, 10, 11). 5. Evoked potentials can be recorded from the brain while stimulating the epidermal lines with weak water movements. The brain potentials differ in several aspects from the potentials of the head lines and show little or no onset or offset wave at the transitions of a frequency and amplitude modulation (Fig. 12).
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