Human detectability of various modulation wave forms in frequency-modulated tones [proceedings].
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Biomedical subjects
Publications and source records attributed to R H Kay.
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1. A method was developed for locating the rostral part of the medial lemniscus in anaesthetized cats and then exploring it with a micro-electrode selective for single axons. Records were made from 165 axons, all shown histologically to lie in the lemniscus.2. Almost all lemniscal axons responded at short latency to a shock through surface electrodes over the dorsal columns at C2. The great majority probably belonged to the dorsal column-lemniscal system, though some may have belonged to other (e.g. spinocervicothalamic) systems.3. Resting discharge was seen in almost all axons in the absence of any stimulation, and must have been generated almost entirely in the relevant relay nuclei, particularly since in many axons it was easily depressed or totally inhibited by appropriately placed mechanical stimulation of skin or a shock to the dorsal columns.4. For each fibre held for an adequate length of time, the receptive field, if accessible, was classified as accurately as possible. Fifty-two axons were precisely categorized in this way: many more were studied for long enough to yield useful information.5. One half (twenty-six) of the best categorized axons had receptive fields suggesting excitation by only one type of receptor: fifteen by tylotrich hairs, four by rapidly adapting tactile foot pad receptors, two by claw movement, two by cutaneous touch corpuscles and three by Type II cutaneous receptors. Rigidly held probes driven by electromechanical transducers were used to establish stimulus/response relations. Adjacent or surround inhibition was seen in nearly all these fields, except for the Type II category.6. The other half (twenty-six) of the best categorized axons showed various degrees of inter-receptive excitatory convergence. Five responded to all types of hair, twelve to hair movement and foot-pad displacement, and nine to hair movement combined with inputs from a variety of slowly adapting receptors in skin or deep tissues, thresholds for the latter ranging from light contact to noxious pressure.7. Forty axons responded with a slowly adapting discharge to joint movement, some with properties suggesting that their receptors did not lie in the joint capsule itself. The high threshold of most of these axons to dorsal column stimulation suggested that the relevant primary axons lay either deep in the dorsal column or in some other tract.8. Of axons whose receptive fields were accurately located, 88% lay in forelimb or upper trunk - the remainder in lower trunk, hind limb or tail. The forepaw accounted for 41% of the former group. Axons with receptively ;pure' properties tended to lie in central or deep parts of the main lemniscal mass at the level studied. Axons responding to joint movement tended to lie deep in the main mass and in the ventromedial lemniscal bundle. There was some clustering of axons with identical receptive properties.
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1. The sensitivity of detecting modulation in a test tone sinusoidally frequency-modulated at a rate varphi(test) is diminished after exposure to a conditioning tone more deeply frequency-modulated at a rate varphi(cond) provided that varphi(cond) is not very different from varphi(test), the sound amplitude being kept constant for each tone at a comfortable hearing level 40-45 dB above threshold.2. When varphi(cond) = varphi(test) the frequency deviation in the modulated test tone must be increased to about three times the unconditioned threshold magnitude to be detectable immediately after exposure to the conditioning tone. Detection sensitivity returns to normal in about one minute.3. At low modulation frequencies the conditioning effects are tuned, being much diminished when varphi(cond) differs from varphi(test) by a few cycles per second.4. Comparing monaural with contra-aural conditioning demonstrates a considerable interaural transfer of about 60-80% of the effect, indicating that the conditioning and its selectivity are predominantly central phenomena.5. The magnitude of the deterioration in detection sensitivity after conditioning is about 3 x at modulation frequencies between about 3/sec and 30/sec. It diminishes at lower and higher modulation frequencies and is effectively absent at 100/sec modulation. The bandwidth of the effect increases from a few cycles per second at the lower end of this range, to some tens of cycles per second at the upper end.6. For the same modulation frequency, the conditioning is relatively insensitive to the mean ;carrier' audiofrequency, f(0). The band width in terms of carrier frequency is at least as wide as ;critical bands'. With a test signal f(0) = 250 Hz, varphi(test) = 8/sec, conditioning is still appreciable for a conditioning tone of varphi(cond) = 8/sec but centred upon f(0) = 150 Hz or = 350 Hz. Conditioning is thus not explicable in terms of coincidences between particular spectral components in the conditioning and test tones.7. Whereas the sensitivity of detecting 8/sec amplitude modulation in a tone is conditioned by prior exposure to either amplitude- or frequency-modulated tones, in contrast the detectability of 8/sec frequency-modulated signals is conditioned only by prior exposure to frequency-modulated tones and not by amplitude-modulated conditioning tones. This underlines the special place of frequency modulation in human audition and emphasizes that the operative stimulus cannot be some aspect common to amplitude modulation and frequency modulation, like identical periodicity or coincident positioning of bands in the integrated spectra of the tones, but points to the instantaneous frequency-modulated wave form as the adequate stimulus.8. These findings strongly suggest that the human auditory pathways contain ;channels' in their organization which determine a final response selectively tuned to particular frequency-modulations. Periodicity coding alone cannot adequately explain this effect which may well only be understood in terms of a ;place' theory of frequency selectivity.9. This organization is well suited to subserve the recognition of frequency-modulation patterns in acoustic signals rather independently of the mean audiofrequency that carries the frequency modulation.
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Coronary angiography remains the standard imaging technique to study coronary artery anatomy. Coronary artery aneurysms and fistulas are often incompletely visualized with routine angiography. Magnetic resonance (MR) imaging of such coronary anomalies is presented. The MR images improve the preoperative assessment of patients with coronary artery aneurysms and fistulas.
Gradient echo signal imaging (GEI) has expanded the clinical role of magnetic resonance (MR) imaging of the heart. The role of GEI to evaluate intracardiac calcified lesions was studied. All patients were imaged with both conventional spin echo (SE) techniques and GEI. The GEI demonstrated that calcific cardiac lesions exhibit magnetic susceptibility differences and produce marked hypointensity throughout the calcified area. All patients had echocardiographic and fluoroscopic evidence of cardiac calcification and surgical confirmation of calcified lesions. The SE MR was unable to define the intracardiac calcification. Gradient echo imaging may be a helpful adjunct in the complete definition of intracardiac calcific lesions. When profound signal void areas are detected on cardiac GEI studies, calcification should be suspected.