卢卡奇的批判思想

G·卢卡奇是20世纪最权威的和最具有独创性的马克思主义思想家之一。说他是一个真正意义上权威的马克思主义者是因为,他的理论是以实践为导向或面向实践的,而且致力于改变世界。当然,这一理论包含着一个内容丰富的理论中介系统——从确立最抽象的方法论和人类学的基础到勾画彻底重建个体社会和共同体的具体方案。但是,对一种理论来说,以实践为导向,首先意味着它必须是批判性的。社会结构、政治制度、社会行为方式、文化领域,都不应被视为可孤立地思考、公正地描述、不考虑价值判断的分析和解释,或可作纯粹理解的既定对象。整个社会领域,包括已经被改造成为我们最接近的环境的那部分自然界,都必须看作是一种人的产品。因此,作为历史的一个阶段,它是满足且也破坏人类渴望的一项未完成的工作。对于任何有意义的人类未来来说,这些生活方式都是不可缺少的。与此同时,它们也有着显著的局限性,即削弱人类所付出的巨大努力,给人类带来连续不断的痛苦和苦难,因此是有待克服的。在辩证的扬弃,(Aufhebung)的这个意义上说,卢卡奇是一位第一流的批判思想家。     

今日维特根斯坦

维特根斯坦在第一次世界大战的战壕中写完他的第一本书——《逻辑哲学论》,当时他在奥地利军队中服役.一系列精雕细刻的格言由一个复杂的排列体系联结起来,并且一切都按照从形而上学到形式逻辑的方向排列.此书被罗素誉为是一部杰作.人们很快就广泛认识到这本书的重要性,特别是通过石里克、卡纳普和魏斯曼,维也纳学派认识到了它的重要性.《逻辑哲学论》立刻使维特根斯坦在哲学家的神殿中占有了一席之地.《逻辑哲学论》是维特根斯坦自己出版的唯一的一本书.有一段时间他放弃哲学去当了一名小学教师,后来又在奥地利做一名建筑师,1929年他回到剑桥,在那里断断续续地工作一直到他1951年去世.他的思想交流实际上仅局限于课堂,他在由学生和同事组成的非常亲密的     

The Timing Effects of Accent Production in Periodic Finger-Tapping Sequences

When subjects are required to produce short sequences of equally paced finger taps and to accentuate one of the taps, the interval preceding the forceful tap is shortened and the one that immediately follows the accent is lengthened. Assuming that the tapping movements are triggered by an internal clock, one explanation attributes the rnistiming of the taps to central factors: The momentary rate of the clock is accelerated or decelerated as a function of motor preparation to, respectively, increase or decrease the movement force. This hypothesis predicts that the interresponse intervals measured between either tap movement onsets or movement terminations (taps) will show the same timing pattern. A second explanation for the observed interval effects is that the tapping movements are triggered by a regular internal clock but the timing of the successive taps is altered because the forceful movement is completed in less time than the other tap movements are. This "peripheral" hypothesis predicts regular timing of movement onsets but distorted timing of movement terminations. In the present study, the trajectories of the movements performed by subjects were recorded and the interresponse intervals were measured at the beginning and the end of the tapping movements. The results of Experiment 1 showed that neither model can fully explain the interval effects: The fast forceful movements were initiated with an additional delay that took into account the small execution time of these movements. Experiment 2 reproduced this finding and showed that the timing of the onset and contact intervals did not evolve with the repetition of trial blocks. Therefore, the assumption of an internal clock that would trigger the successive movements must be rejected. The results are discussed in the framework of a modified two-stage model in which the internal clock, instead of triggering the tapping movements, provides target time points at which the movements have to produce their meaningful effects, that is, contacts with the response key. The timing distortions are likely to reflect both peripheral and central components.     

Residence time and choice in concurrent foraging schedules

Five pigeons were trained on a concurrent-schedule analogue of the “some patches are empty” procedure. Two concurrently available alternatives were arranged on a single response key and were signaled by red and green keylights. A subject could travel between these alternatives by responding on a second yellow “switching” key. Following a changeover to a patch, there was a probability (p) that a single reinforcer would be available on that alternative for a response after a time determined by the value of λ, a probability of reinforcement per second. The overall scheduling of reinforcers on the two alternatives was arranged nonindependently, and the available alternative was switched after each reinforcer. In Part 1 of the experiment, the probabilities of reinforcement, ρ_red and ρ_green, were equal on the two alternatives, and the arranged arrival rates of reinforcers, λ_red and λ_green, were varied across conditions. In Part 2, the reinforcer arrival times were arranged to be equal, and the reinforcer probabilities were varied across conditions. In Part 3, both parameters were varied. The results replicated those seen in studies that have investigated time allocation in a single patch: Both response and time allocation to an alternative increased with decreasing values of λ and with increasing values of ρ, and residence times were consistently greater than those that would maximize obtained reinforcer rates. Furthermore, both response- and time-allocation ratios undermatched mean reinforcer-arrival time and reinforcer-frequency ratios.