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Entities and Brain Organization: Logogenesis of Meaningful Time-Forms 实体与大脑组织:有意义时间形式的意义起源
Pub Date : 2018-10-24 DOI: 10.4324/9781315789347-37
M. Clynes
The central nervous system function of time-form entities are examined. The term Logogenesis is introduced as a concept to denote genetically programmed development of mental concepts and time form-entities, as a counterpart to morphogenesis which concerns development of structure. Special attention is given to the time-form logogenesis of natural language entities of emotion communication, and their natural syntax. How time-forms are used in music to generate living, meaningful performances from written scores is described and proved with computer generated classical music, in the context of four modes of time experience, t1, t2, t3, and t4. The modes apply to different time scales and use different natural data processing properties. Models of appropriate peptide dynamics are suggested for some of these amygda-related processes. Some properties of modified time consciousness in relation to these modes are also discussed.
研究了时间形式实体的中枢神经系统功能。“理性发生”一词是作为一个概念引入的,表示心理概念和时间形式实体的基因程序化发展,与涉及结构发展的形态发生相对应。特别关注情感交际的自然语言实体的时间形式语源及其自然句法。在t1、t2、t3和t4四种时间体验模式的背景下,用计算机生成的古典音乐描述并证明了音乐中如何使用时间形式从书面乐谱中产生生动、有意义的表演。这些模式适用于不同的时间尺度,并使用不同的自然数据处理特性。对于其中一些与杏仁核相关的过程,提出了适当的肽动力学模型。还讨论了修正的时间意识与这些模式有关的一些性质。
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引用次数: 1
The Perception of Visual Form 视觉形式的感知
Pub Date : 2018-10-24 DOI: 10.1037/H0067147
C. H. Judd
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引用次数: 1
Dynamic Self-Organization in the Brain as Observed by Transient Cortical Coherence 大脑的动态自组织是由短暂的皮层一致性观察到的
Pub Date : 2018-10-24 DOI: 10.4324/9781315789347-30
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引用次数: 1
Cooperative Behavior in the Periodically Modulated Wiener Process 周期调制Wiener过程中的合作行为
Pub Date : 2018-10-24 DOI: 10.4324/9781315789347-22
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引用次数: 0
Spectral Density Maps of Receptive Fields in the Rat's Somatosensory Cortex 大鼠体感皮层受体场的谱密度图
Pub Date : 2018-10-24 DOI: 10.4324/9781315789347-32
Joseph S. King, M. Xie, B. Zheng, K. Pribram
To extend fmdings from visual neurophysiology we plotted responses for 48 locations in the somatosensory "barrel cortex" of the rat to spatial and temporal frequency stimulation of their vibrissae. The recordings obtained from bursts of spikes were plotted as response manifolds resembling field potentials such as those recorded with small macroelectrodes. The burst manifolds were shown to be composed of those obtained from single spikes, demonstrating continuity between two levels of analysis (single spikes and bursts). A computer simulation of our results showed that, according to the principles of signal processing, the somatosensotyreceptive fields can be readily described by Gabor-like functions much as in the visual system. Further, changes with respect to direction of whisker stimulation could be described in terms of spatiotemporal (vectorial?) shifts among these functions. As late as the 1950's, the structure of memory storage and the brain processes leading to perception remained enigmatic. Thus Karl Lashley (1950) could exclaim that his lifelong search for an encoded memory trace had been in vain, and Gary Boring (1929) could indicate in his History of Experimental Psychology that little was to be gained, at this stage of knowledge, by psychologists studying brain function. All this was dramatically changed when engineers, in the early 1960's, found ways to produce optical holograms using the mathematical fonnulation proposed by Dennis Gabor (1948). The mathematics of holography and physical properties of holograms provided a palpable instantiation ofdistributed memory and how percepts (images) could be retrieved from such a distributed store. Engineers, (e.g. Van Heerden, 1963) psychophysicists, (e.g. Julez and Pennington, 1965); and neuroscientists, (e.g. Pribram, 1966; and Pollen, Lee and Taylor, 1971) saw the relevance of holography to the hitherto intractable issues of brain function in meqlory and perception (Barrett, 1969; Campbell & Robson, 1968; and Pribram, Nuwer and Barron, 1974). However, this early promise failed, for a variety of reasons, to take hold in the scientific community. The fact that neurophysiologically the holographic spread function is limited to single, albeit overlapping, receptive fields (patches) was not recognized by psychophysicists who, therefore, spent considerable energy in disproving globally conceived distributed functions. However, engineers, e.g. Bracewell (see review, 1969), soon showed that such patch holography could and did produce correlated three-dimensional images when inverse transformed, a technique that became the basis of optical image processing in tomography. The application of this principle to the receptive field structure (Robson 1975) overcame the psychophysical problem. Further, it was unclear just how the principles involved in holography related to ordinary measures of brain physiology. For instance, the brain waves recorded with scalp electrodes are too slow to carry the requi
为了扩展视觉神经生理学的发现,我们绘制了大鼠体感“桶状皮层”的48个位置对其触须的空间和时间频率刺激的反应。从尖峰爆发中获得的记录被绘制成响应流形,类似于用小宏电极记录的场电位。突发流形被证明是由单峰值得到的流形组成的,证明了两个分析水平(单峰值和突发)之间的连续性。计算机模拟我们的结果表明,根据信号处理的原理,体感感受野可以很容易地用gabor样函数来描述,就像在视觉系统中一样。此外,有关晶须刺激方向的变化可以用这些功能之间的时空(矢量?)变化来描述。直到20世纪50年代,记忆储存的结构和导致感知的大脑过程仍然是个谜。因此,卡尔·拉什利(1950)可以惊呼,他一生对编码记忆痕迹的探索是徒劳的,加里·博林(1929)可以在他的《实验心理学史》中指出,在知识的这个阶段,心理学家研究大脑功能的收获很少。20世纪60年代早期,工程师们发现了利用Dennis Gabor(1948)提出的数学公式制作光学全息图的方法,这一切都发生了戏剧性的变化。全息术的数学和全息图的物理特性提供了分布式记忆的明显实例,以及如何从这种分布式存储中检索感知(图像)。工程师(如Van Heerden, 1963)心理物理学家(如Julez和Pennington, 1965);和神经科学家,(如Pribram, 1966;和Pollen, Lee和Taylor, 1971)看到了全息摄影与迄今为止难以解决的大脑记忆和感知功能问题的相关性(Barrett, 1969;Campbell & Robson, 1968;Pribram, Nuwer和Barron, 1974)。然而,由于种种原因,这一早期的承诺未能在科学界站稳立场。事实上,从神经生理学上讲,全息传播功能仅限于单个,尽管重叠,接受野(斑块)没有被精神物理学家认识到,因此,他们花了相当多的精力来反驳全球构思的分布式功能。然而,工程师,如Bracewell(见回顾,1969),很快就表明,这种补丁全息术可以并且确实在逆变换时产生相关的三维图像,这种技术成为断层摄影中光学图像处理的基础。将这一原理应用于感受野结构(Robson 1975)克服了心理物理问题。此外,当时还不清楚全息摄影的原理是如何与大脑生理学的普通测量相关联的。例如,头皮电极记录的脑电波太慢,无法承载所需的充血量。此外,似乎很少有证据表明,在大脑皮层的感受野特性中可以发现进行傅立叶全息移植的基本正交关系。最后,关于什么需要被编码来提供一个神经全息过程有相当大的困惑。这些反对意见在很大程度上得到了满足。神经微管的纳米电路为突触树突感受野的微处理提供了足够的高频波形(例如Hammeroff, 1987)。四分形在视觉皮层的接受区显示出来(Pollen and Ronner, 1980)。而且,波之间的交点系数的编码,而不是波本身的编码,对这个过程至关重要(Pribram, 1991)。尽管有这些证据,Churchland(1986)反映了神经科学界的普遍观点,他指出:“大脑就像一个全息图,因为信息似乎分布在一组神经元上。然而,除此之外,全息思想并没有真正设法解释存储和检索现象。尽管在发展这一类比方面付出了巨大的努力(例如,参见Longuet-Higgins, 1966),但它并没有发展成为一种可信的对数据存储、检索、遗忘等过程的描述。全息图的数学似乎也没有打开通往神经系统数学的大门。这个比喻做到了。尽管如此。启发平行脑功能建模的研究”(第407-408页)。同样的道理。Arbib(1969)指出:“……我们注意到,剑桥心理物理学院(见坎贝尔,1974年对他们工作的早期回顾)的心理物理数据表明,视觉皮层的细胞对特定宽度的条形或特定空间频率的栅格的反应不如对边缘的反应多。 视觉皮层的空间频率调节细胞可以被视为落在不同的通道取决于他们的空间调节。这似乎支持了大脑提取视觉图像的空间傅里叶变换的论点。然后将其用于全息存储或与位置无关的识别(Pribram, 1971)。然而,没有证据表明神经系统具有空间频率的精细辨别或空间相位信息的保存,从而使这种傅里叶变换的计算具有足够的精度,从而有用”(第134-135页)。这一观点也进入了关于这一主题的通俗文学。为例。克里克(1994)指出“大脑和全息图之间的类比经常被那些对两者都知之甚少的人热情地接受。这几乎肯定是没有回报的。有两个原因。一项详细的数学分析表明,神经网络和全息图在数学上是不同的。更重要的是。尽管神经网络是由与真实神经元有一些相似之处的单元构建而成,但在大脑中却找不到这种装置或过程的痕迹;全息摄影是必需的。”(需要)。=;在如此多的相反证据的情况下,可以做出这样的陈述——例如,参见Devalois和Devalois(1988)和Pribram(1991)的著作——这表明,在公认的观点和那些为另一种观点提供证据的人之间,存在着一些基本的分歧。我们认为全息原理在神经生理学上的失败是由于被认为是大脑处理介质的原因:神经元的集合或突触树突树枝的重叠(接受)场。这种区别很微妙。一个和关注的是~ 'f>'处理被设想发生的水平或规模。神经元集合作为系统(电流,术语是“模块”),通过axo - s进行通信,确实起着重要的作用:例如,在局部临床残疾所表明的信息检索中。尽管如此,在模块中,处理依赖于分布式架构,例如神经网络模拟中使用的那些。我们的论点是,在这种处理水平上,集合不是由神经元组成的,而是由突触树突网络的斑块组成的。我们需要的是一种方法来绘制重叠的突触-树突接受野的活动,以使科学界相信,在突触-树突水平上确实存在着类似全息过程的东西。Kuffler(1953)为我们提供了一个重大突破,他展示了他可以通过记录视神经的轴突来绘制视网膜神经节细胞的树突区域的一部分。Kuff1~r是一种简单的技术,用于制作接受域图,这是现在神经生理学的标准技术。通过在不同维度上刺激一个受体或一组受体,并利用从轴突记录的单位反应密度,可以获得该轴突突触树突接受野的功能组织图。(参见Bekesy(1967)和Connor and Johnson(1992)的评论;Enroth-Kugel和Robson, 1966;Rodiek和Stone, 1965年的视觉)。, . Barlow(1986)以及Gilbert和Wiesel(1990)的实验表明,在特定条件下,超出特定神经元接受野范围的感觉刺激可以改变该神经元的轴突反应。因此,突触树突斑块受邻近突触树突电场中更广泛的电位场所产生的变化的影响。很少认识到的是,kuffler1技术绘制了发生在这种扩展重叠树突乔木中的局部场电位之间的关系。产生记录的轴突,从这个重叠的接受区扩展区域中抽取有限的一小块样本。最近,Varella(1993)通过证明从轴突记录的突发活动与该轴突突触树突感受野产生的局部场电位之间的相关性,引起了人们对这种关系的关注。本研究还利用Kuffler技术绘制感受野组织图,探讨局部场电位之间的关系。提出并给出肯定答案的具体问题是:1)该技术是否可以绘制突触树突感受野电位的光谱特性,以及2)这种体感皮层感受野的图谱是否显示出与视觉皮层记录的图谱相似的补丁(量子)全息(即Gabor基本功能)特性。 方法和结果选择大鼠体感觉系统是为
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引用次数: 1
Consciousness and Anesthesia: An Hypothesis Involving Biophoton Emission in the Microtubular Cytoskeleton of the Brain 意识和麻醉:一个涉及脑微管细胞骨架中生物光子发射的假说
Pub Date : 2018-10-24 DOI: 10.4324/9781315789347-12
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引用次数: 1
Perception. Double Dichotomy of Visual Brain 感知。视觉脑的双重二分法
Pub Date : 2018-10-24 DOI: 10.4324/9781315789347-34
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引用次数: 0
Noise and the Neurosciences: A Long History, a Recent Revival and Some Theory 噪音与神经科学:悠久的历史,最近的复兴和一些理论
Pub Date : 2018-10-24 DOI: 10.4324/9781315789347-20
J. Segundo, J. Vibert, K. Pakdaman, Michael Stiber, O. D. Martínez
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引用次数: 13
Cloning and embryonic stem-cells: ballot initiative opposed. 克隆和胚胎干细胞:投票倡议反对。
Pub Date : 2006-10-19
Raymond Burke, Robert Finn, John Gaydos, John Leibrecht, Robert Hermann, Raymond Boland
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引用次数: 0
Those who don't receive medical care. 那些得不到医疗照顾的人。
Pub Date : 2006-06-22
Carol Keehan
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引用次数: 0
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Origins
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