复变函数论教学内容与教学方法的新探

随着高中数学教材内容的不断更新,高师院校复变函数论课程内容和教学方法的调整势在必行。本文在分析现状的前提下,就复变函数论课程内容和教学方法进行了一些有益的探索。     

回收碘的研究

主要介绍了磷化工厂含碘烟气中碘元素通过富集，沉淀回收的方法。对碘的回收的影响因素很多，主要讨论温度、pH值、沉淀剂的种类与碘回收的关系，并且通过实验找出最佳的工艺参数并确定经济合理、适用性广的工艺流程。     

可变分区存储管理方式的模拟

论述了如何用C语言模拟可变分区存储管理方式的过程。形象地展示了操作系统中可变分区存储管理中采用的最佳适应算法的分配与回收过程，达到了理论与实践相联系的目的。     

基于语言偏好的群体决策的软解法

群体决策模型用于支持系统或专家系统，面临的两个问题是：自然语言与机器语言的匹配以及模型解与决策者意向交融．本文在许多学者大量工作的基础上，试图提出群决策的软化求解模型．主要提出两方面的结果：一是多准则语言偏好的综合；二是采用模糊匹配方法和语言变量的软算法将个人语言偏好聚集为群体可接受决策解．最后给出实例计算以说明操作步骤．该模型可用于人－机交流式ＧＤＳＳ或小群（７～１２人）会议支持系统的软件设计     

成本性态法在分析可比产品成本降低计划完成情况中的应用

本文根据成本性态法的思路．分析了影响可比产品成本降低额和降低率变动的因素，重点从理论上论证了产品品种结构的影响，并且合理地把单纯产量和品种结构对可比产品成本降低额（率）的影响分离开来．     

智能化44点啤酒发酵温度巡测仪

本文将八十年代最新研制的集成温度传感器ＡＤ５９０、８０９０单片机，可编程逻辑器件ＧＡＬ－１６Ｖ８Ａ等新器件及智能化新技术，集中应用于啤酒发酵过程的温度检测。与传统人工测温相比，具有测温精度高、稳定性好、反应快、可远距离自动检测、定时打印，减轻工人劳动强度、调节啤酒发酵温度的响应速度快等特点。     

切削刀具倒棱刃口挤压力的理论计算

根据试验观察．揭出了刀具刃口带负倒棱时的切削模型。在此模型中,刀具刃口 存在一个“金属死区”。以新模型为基础．采用能量法,对高温、高应变率下刀具刃 口的挤压力进行了理论计算。所做工作的特点是：１）在材料变形分析中计入了挤压 层金属绕过刀具刃口时的过剩变形;２）进行有关材料变形与物理特性的计算时,考 虑了温度与应变率的影响。利用新研制的压电式切削测力仪进行验证试验,其结果表 明,理论计算值与实测数据较好一致。     

The induction of secondary seed dormancy by oxygen deficiency in a barnyard grassEchinochloa crus-galli

At 25°C, secondary dormancy was induced in seeds ofE. crus-galli exposed for 100 days to oxygen deficiency. By contrast, hypoxia did not induce dormancy at 15°C or prevent dormancy termination at 7°C. Secondary dormancy was terminated after 2 months stratification at 7°C. Oxygen deficiency may increase the proportion of dormant seeds in the soil, and affect the dynamics of the barnyard-grass soil seed bank.We thank Miss Jitka Králová for her excellent technical assistance.     

Internal interactions within the human circadian system: the masking effect

Summary In the realm of human circadian rhythms, the masking effect is defined as the change in the course of deep body temperature induced by changes in the degree of physical activity, or by the alteration between sleep and wake. This effect is particularly obvious during internal desynchronization where the rhythms of deep body temperature, and the sleep-wake sleep-wake sleep cycle — i.e. one of the masking factors — run with different periods.Every sleep onset is accompanied by a rapid drop, and wake onset by a rapid rise in deep body temperature, each one with an overshoot of about 50% of the steady state variations. When rhythms are calculated, with the dominant temperature period as the screening period, exclusively from data obtained during sleep episodes, on the one hand, and from those obtained exclusively during wake, on the other, two average cycles emerge: the sleep temperature curve and the wake temperature curve. Both run in parallel but are separated by the masking effcct. As derived from many experiments, the mean masking effect amounts to 0.28±0.06°C. The masking effect also depends to some extent on the phase of the temperature rhtthm; it is larger than average around the temperature maximum and during the descending phase of the temperature cycle, where the alertness commonly is highest and the probability to sleep, in general, and the REM sleep propensity, in particular, are smaller than average. This also can be interpreted to indicate that the sleep temperature curve is phase advanced relative to the wake temperature curve; this, on the average, by 0.9±0.3 h.If the individually determined amount of masking is added to the temperature data obtained during sleep, or substracted from the temperature data obtained during wake, a temperature curve emerges that can be though of as being purified of the masking effect. Analyses of this artificial curve allow estimation of that part of the internal interactions uninfluenced by the masking effect. On the average, about half of the amount of interaction between the rhythm of sleep-wake and that of deep body temperature is explained by the masking effect, whereas the other half is oscillatory interaction. Both types of interaction are inherent and inseparable parts of the circadian clock mechanism, as can be deduced from model considerations.     

Photoperiodic summation is temperature-dependent inPyrrhocoris apterus (L.) (Heteroptera)

Summary InPyrrhocoris apterus, a low temperature, 15°C, prevented the termination of diapause by long days and, unexpectedly, also the induction of diapause by short days. Both responses were enabled at a higher temperature, 26°C. In contrast to current concepts, it was proved that the summation of photoperiodic signals was temperature-dependent, since the morphogenetic development was prevented by starvation.