Guillery et al. (109) argued that these retinorecipient cells are an extension of the lateral geniculate nucleus and called them the "geniculate wing." Since these cells receive inputs from the retina (15, 17, 169, 188, 219) and project to the cortex (1?,161,169,1'79), it seems proper to consider them part of the lateral geniculate nucleus. We therefore adopt the terminology of Guillery et al. (109) and refer to them as the geniculate wing in this review.
A superconducting chip containing a regular array of flux qubits, tunable interqubit inductive couplers, an XY-addressable readout system, on-chip programmable magnetic memory, and a sparse network of analog control lines has been studied. The architecture of the chip and the infrastructure used to control it were designed to facilitate the implementation of an adiabatic quantum optimization algorithm. The performance of an eight-qubit unit cell on this chip has been characterized by measuring its success in solving a large set of random Ising spin glass problem instances as a function of temperature. The experimental data are consistent with the predictions of a quantum mechanical model of an eight-qubit system coupled to a thermal environment. These results highlight many of the key practical challenges that we have overcome and those that lie ahead in the quest to realize a functional large scale adiabatic quantum information processor.
Efforts to develop useful quantum computers have been blocked primarily by environmental noise. Quantum annealing is a scheme of quantum computation that is predicted to be more robust against noise, because despite the thermal environment mixing the system's state in the energy basis, the system partially retains coherence in the computational basis, and hence is able to establish well-defined eigenstates. Here we examine the environment's effect on quantum annealing using 16 qubits of a superconducting quantum processor. For a problem instance with an isolated small-gap anticrossing between the lowest two energy levels, we experimentally demonstrate that, even with annealing times eight orders of magnitude longer than the predicted single-qubit decoherence time, the probabilities of performing a successful computation are similar to those expected for a fully coherent system. Moreover, for the problem studied, we show that quantum annealing can take advantage of a thermal environment to achieve a speedup factor of up to 1,000 over a closed system.
The visual receptive fields of 213 cells in the lateral suprasylvian visual cortex (LS, or Clare-Bishop area) were studied in cats anesthetized with nitrous oxide. Eighty-one percent of the cells were directionally selective. They responded poorly to stationary stimuli flashed on or off, but gave a directionally selective response to stimuli moving through the receptive field. Most of these had a single preferred direction and an opposite null direction. They typically responded to a range of directions of stimulus movement from 45 to 90 degrees to either side of the preferred direction. Small stimuli (1-2 degrees or smaller) typically were effective and 87% of the directionally selective cells showed spatial summation. About 32% had inhibitory mechanisms which decreased the response of the cell if the stimulus exceeded a maximum size. There was little or no evidence that LS area cells were orientation selective or sensitive to variations in stimulus shape independent of size.
It is now well appreciated that parallel retino-geniculo-cortical pathways exist in the monkey as in the cat, the species in which parallel visual pathways were first and most thoroughly documented. What remains unclear is precisely how many separate pathways pass through the parvo- and magnocellular divisions of the macaque lateral geniculate nucleus (LGN), what relationships-homologous or otherwise-these pathways have to the cat's X, Y, and W pathways, and whether these are affected by visual deprivation. To address these issues of classification and trans-species comparison, we used achromatic stimuli to obtain an extensive set of quantitative measurements of receptive field properties in the parvo- and magnocellular laminae of the LGN of nine macaque monkeys: four normally reared and five monocularly deprived of vision by lid suture near the time of birth. In agreement with previous studies, we find that on average magnocellular neurons differ from parvocellular neurons by having shorter response latencies to optic chiasm stimulation, greater sensitivity to luminance contrast, and better temporal resolution. Magnocellular laminae are also distinguished by containing neurons that summate luminance over their receptive fields nonlinearly (Y cells) and whose temporal response phases decrease with increasing stimulus contrast (indicative of a contrast gain control mechanism). We found little evidence for major differences between magno- and parvocellular neurons on the basis of most spatial parameters except that at any eccentricity, the neurons with the smallest receptive field centers tended to be parvocellular. All parameters were distributed unimodally and continuously through the parvo- and magnocellular populations, giving no indications of subpopulations within each division. Monocular deprivation led to clear anatomical effects: cells in deprived-eye laminae were pale and shrunken compared with those in nondeprived eye laminae, and Cat-301 immunoreactivity in deprived laminae was essentially uniformly abolished. However, deprivation had only subtle effects on the response properties of LGN neurons. Neurons driven by the deprived eye in both magno- and parvocellular laminae had lower nonlinearity indices (i.e., summed signals across their receptive fields more linearly) and were somewhat less responsive. In magnocellular laminae driven by the deprived eye, neuronal response latencies to stimulation of the optic chiasm were slightly shorter than those in the nondeprived laminae, and receptive field surrounds were a bit stronger. No other response parameters were affected by deprivation, and there was no evidence for loss of a specific cell class as in the cat.
Visual abilities decline during aging, and many of these declines are due to neural changes in the retina or brain. We have begun studies of the monkey visual system to investigate the location and nature of these changes as well as to answer general questions about the effects of aging on neural structure and function. We began with the dorsal lateral geniculate nucleus (LGN) because it is the main structure through which visual information passes on the way to cortex and because the parallel parvicellular and magnocellular pathways are most easily identified and studied in the LGN. In the present experiment, we determined the sizes, densities, and numbers of LGN neurons in young-adult (5 to 12.5 years) and old (23 to 27.5 years) rhesus monkeys. The measures were corrected for tissue shrinkage, and stereological procedures were used that yield unbiased estimates. In young-adult monkeys, neurons densities were lower in the magnocellular layers (about 14,000/mm3) than in the parvicellular layers (23,000/mm3). Neuron density increased about 28% from anterior to posterior in both types of layers. There was an average of approximately 1,267,000 neurons in the parvicellular layers and 148,000 neurons in the magnocellular layers; however, there was substantial variability (1.9-fold) among five brains studied. Aging produced a statistically significant decrease in neuron density in both the magnocellular (29% average decrease) and parvicellular (41% average decrease) layers. However, there was no significant loss of neurons. Rather, the density decrease was due to a small (nonsignificant) decrease in the number of neurons combined with a small (nonsignificant) increase in LGN volume. The increase in LGN volume was due to a significant increase in neuron soma-size and proportional increase in the volume of glial cells, blood vessels, and neuropil. These results, together with those of other studies, suggest that the effects of aging on the primate visual pathway from retina through striate cortex are relatively subtle. It is possible that the major neural changes occur more centrally. Alternatively, individual differences in the effect of aging may require much larger samples or prior screening to observe consistent changes.
1. Visual abilities decline during normal aging, and many of these declines are due to neural changes in the retina or central visual pathways. We have begun studies of the primate visual system to investigate the location and nature of these changes as well as to answer general questions about the effects of aging on neural function. We began with the dorsal lateral geniculate nucleus (LGN) because it is the main structure through which visual information passes on the way to cortex and because the parallel parvocellular and magnocellular pathways, which may be affected differently by aging, are anatomically distinct there. 2. Single -cell recordings were made in the LGN of young adult (5–16 yr) and old (25–28 yr) rhesus monkeys. We made quantitative measures of a wide variety of response properties for a large number of parvocellular (n = 257) and magnocellular (n = 113) neurons in the two groups of animals. As a result, in addition to studying the effects of aging, we were able to make quantitative comparisons between parvocellular and magnocellular neurons using larger samples than have been studied previously and for some properties that have not been studied before. 3. We found that magnocellular neurons have significantly higher maximal response rates and signal -to -noise ratios than parvocellular neurons. However, response latencies to visual stimulation were similar for neurons in the two types of layers. In agreement with previous studies, magnocellular neurons had higher maximal contrast sensitivity and higher contrast gain than parvocellular neurons. However, the sensitivity difference occurred because nearly all of the neurons with low sensitivities (< 10) were in the parvocellular layers, not because neurons in the magnocellular layers had the highest sensitivities. 4. Neurons with the smallest receptive-field centers, the highest spatial-frequency resolutions, and the highest optimal spatial frequencies were found in the parvocellular layers. However, the overall distributions of each of these properties overlapped substantially for neurons in the two types of layers, and the mean values were not significantly different. The mean high temporal-frequency cutoff was significantly higher for magnocellular than parvocellular neurons, but the difference was small (only 3 Hz), and it occurred because many parvocellular neurons had lower cutoffs than any seen in the magnocellular layers, not because magnocellular neurons had the highest temporal-frequency cutoffs. Parvocellular neurons also had narrower temporal-frequency tuning than magnocellular neurons. However, there was no significant difference in optimal temporal frequency.(ABSTRACT TRUNCATED AT 400 WORDS)
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