生产与交往——或马克思与哈贝马斯

在今天这个已变得如此狭小的世界上,我们所面临的全球性问题,尤其是核灾难对人类的威胁,要求在各民族之间建立起一种理性的共存格局。从现实主义角度来看,用理性来协调人们的行为举止,不是由于其自身,而是由于明显的物质方面的生存危机,今天具有前所未见的发展机遇。最迟自十八世纪启蒙运动开始,科学已经被看作是最佳的理性     

科学的统一

1.分类与系统论自有了科学以来,自有了欧洲哲学以来,人们就梦想着科学的统一,梦想着能有一个统一的科学体系。即使在科学哲学创立之前,希腊人的思想就发展到了这一步,即认为甚至科学和哲学也能构成一种哲学的统一。这种观点的影响早已烟消云散了。今天,在这种观点一度占支配地位的那些领域中,我们不断发现了一些未曾阐述清楚的经验关系和系统关系。我们不再讨论科学(与或不与哲学)的统一,而是讨论学科性、多学科性和学科间性,抚昔追今,我们所探讨的知识秩序已不再能用知识本     

罗素与实用主义者

罗素与他曾遇见过的,并就哲学问题进行过交流的好几位实用主义哲学家相互影响。这些相互影响同罗素与他的朋友和合作者如摩尔、怀特海、维特根斯坦等之间的相互影响性质不同。这是一种敌对的性质。事实上罗素与唯心主义者的相互影响也是如此。不同的地方只在于罗素本人曾经历新黑格尔主义这一阶段。至于就实用主义来说,罗素自始至终把它作为对手,实用主义者的主张对他来说是不相容的。尽管罗素自己思想发展过程中在这一点上没有改变过,但是,正如我们将看到的,他思想上的变化使他比他自己承认的更接近这些实用主义的观点。1896年,罗素在他第一次访问美国时结识了詹姆斯和皮尔斯。后来罗素又从W.维尔比(Welb     

创造性思维与创造力培养的概念

创造性思维是适应性思维或称重新概念化。其绝大部分不是外显行为,而是内隐的认知。我们日常大部分认知和行为是自动化的。它们满足着我们的日常需要。而满足我们需要的方式有一定导向,甚至变得刻板严格。在我们日常生活的所有方面,象饮食社交、宗教艺术、学术训练等等,我们都发展了动作的、自动化的认知和行为来满足基本的需要。我们去餐馆吃饭来满足饥饿的需要,与亲属的社会交往在家庭团聚中已经仪式化,我们的医生每月     

系统属性的产生问题

《哲学问题》1992年第2期上刊登了C.и.雅科夫连柯一篇内容丰富的文章《论自然界中的组织作用和破坏(随机的)作用,该期还登载了B.и.阿尔申诺夫和я.и.斯维尔斯基的文章《从涵义的读出到涵义的产生》。按照编辑部的意图,后一篇文章大概是前一篇文章的评论。但我以为,这篇文章并没有起到多大的评论作用,因为这篇论涵义的有趣     

人对动物有道德义务吗?

自从10年以前彼得·辛格的《动物解放》一书出版以来,在英国人的书籍中便对动物的道德处境的问题展开了激烈的讨论,在这期间,这个问题也在我们国家引起了较大的重视。从历史上看,这种关心无疑是对于自然的新意识的结果,而这种对于自然的新意识又是由于那些不能再忽视的生态问题产生的。可是按照事情的性质,我们这里所谈的与两个不同的问题有关。适当同自然环境打交道的问题是个我们共同的切身利益的问题,不是一种“生态     

Additional-delay schedules: A continuum of temporal contingencies by varying food delay

Pigeons performed on discrete-trial, temporally defined schedules in which the food delay (D) was adjusted according to the latency of the key peck (X) and two schedule parameters (t and A). The schedule function was D = A(t − X), where D is the experienced delay between a response and a reinforcer. The schedule parameter t is the maximum value below which the present contingencies occur. A is the additional delay to reinforcement for each second the response latency is shorter than the t value. When A = 0 s, the schedule is a continuous reinforcement schedule with immediate reinforcement. When A = 1 s, the schedule is a conjunctive fixed-ratio 1 fixed-time t-s schedule. When A approaches infinity, the schedule becomes a differential reinforcement of long latency schedule. The latencies for subjects with t = 10 s and t = 30 s were observed with the present schedules having seven values for A between 0 s and 11 s. In addition, the latencies for subjects for which t = 30 s were observed at an A value of 31 s to 41 s. As the A value increased, the latencies approached the t value for subjects for which t = 10 s. The latencies for 30-s-t subjects did not approach t, even when the A value was 41 s. The latencies for 10-s-t subjects at 11-s A value were longer than those under yoked conditions having exactly the same delays/interreinforcement intervals. These results demonstrated a continuum of latency related to the schedule continuum (value of A) at a small t value.     

Determinants of pigeons' waiting time: Effects of interreinforcement interval and food delay

Four pigeons performed on three types of schedules at short (i.e., 10, 30, or 60 s) interreinforcement intervals: (a) a delay-dependent schedule where interreinforcement interval was held constant (i.e., increases in waiting time decreased food delay), (b) an interreinforcement-interval-dependent schedule where food delay was held constant (i.e., increases in waiting time increased interreinforcement interval), and (c) a both-dependent schedule where increases in waiting time produced increases in interreinforcement interval but decreases in food delay. Waiting times were typically longer under the delay-dependent schedules than under the interreinforcement-interval-dependent schedules. Those under both-dependent schedules for 1 subject were intermediate between those under the other two schedule types, whereas for the other subjects waiting times under the both-dependent procedure were similar either to those under the delay-dependent schedule or to those under the interreinforcement-interval-dependent schedule, depending both on the subject and the interreinforcement interval. These results indicate that neither the interreinforcement interval nor food delay is the primary variable controlling waiting time, but rather that the two interact in a complex manner to determine waiting times.     

Theories of early language acquisition

What features of brain processing and neural development support linguistic development in young children? To what extent is the profile and timing of linguistic development in young children determined by a pre-ordained genetic programme? Does the environment play a crucial role in determining the patterns of change observed in children growing up? Recent experimental, neuroimaging and computational studies of developmental change in children promise to contribute to a deeper understanding of how the brain becomes wired up for language. In this review, the muttidisciplinary perspectives of cognitive neuroscience, experimental psycholinguistics and neural network modelling are brought to bear on four distinct areas in the study of language acquisition: early speech perception, word recognition, word learning and the acquisition of grammatical inflections. It is suggested that each area demonstrates how linguistic development can be driven by the interaction of general learning mechanisms, highly sensitive to particular statistical regularities in the input, with a richly structured environment which provides the necessary ingredients for the emergence of linguistic representations that support mature language processing. Similar epigenetic principles, guiding the emergence of linguistic structure, apply to all these domains, offering insights into phenomena ranging from the precocity of young infant's sensitivity to speech contrasts to the complexities of the problem facing the young child learning the arabic plural.