高温高压下岩石部分熔融及熔体形态学研究

熔体形态学作为现代岩石学的前沿领域之一，其主要研究矿物颗粒之间熔体形态特征、连通性以及与周围矿物的相互作用关系。该学科在我国还不被广大地学工作者所熟悉。本论文以斜长角闪岩为初始物料，在850-1100℃和2.0-4.0 GPa条件下，进行了岩石的部分熔融实验，并对作为实验产物的熔体进行了形态学方面的研究。同时就目前形态学研究的基础理论和实验方法作了初步介绍。 利用YJ－3000吨六面顶高压装置，我们以天然的块状斜长角闪岩为样品，在高温高压条件下进行了斜长角闪岩的脱水部分熔融实验，测量了熔体与矿物相接触时所形成的二面角。结果表明： 1、熔体的形态分布与熔融程度具有明显依赖关系，当熔融程度小于5%时，熔体被矿物颗粒分隔开来，以熔块的形式相互独立；当熔融程度大于5%时，薄膜状或管状熔体沿矿物颗粒边缘形成一个相互连通的熔融网络。 2、当熔体相互隔离时，二面角平均值大于60°；当熔体相互连通时，二面角平均值小于60°。在熔体相互连通的测量实验中，英安质和安山质成分的熔体与石榴子石的二面角分布在56－58°之间，与单斜辉石的二面角分布在50－53°之间。 3、根据界面化学理论推导表面张力和界面能的最小化是推动熔体连通的两个驱动力。 4、二面角大小受体系温度、压力及物质组成等物理化学条件的影响，随着温度升高，固－液界面的表面张力减弱，二面角减小，熔体越容易相互连通。 5、通过对二面角的原位测量，不仅可以判断熔体的相互连通性，还能反演熔体的熔融过程。

阿片药物依赖的神经机制---内侧前额叶与药物的心理依赖

Mental dependence, characterized by craving and impulsive seeking behavior, is the matter of intensive study in the field of drug addiction. The mesolimbic dopamine system has been suggested to play an important role in rewarding of drugs and relapse. Although chronic drug use can induce neuroadaptations of the mesolimbic system and changes of drug reinforcement, these mechanisms cannot fully account for the craving and the compulsive drug-using behavior of addicts. Acknowledging the reinforcement effects of drugs, most previous studies have studied the impact of environmental cues and conditioned learning on addiction behavior, often using established classical or operant conditioning model. These studies, however, paid little attention to the role of cognitive control and emotion in addiction. These mental factors that are believed to have an important influence on conditioned learning. The medial prefrontal cortex (mPFC) has close anatomic and functional connections with the mesolimbic dopamine system. A number of the cognitive neurological studies demonstrate that mPFC is involved in motivation, emotional regulation, monitoring of responses and other executive functions. Thus we speculated that the function of abnormality in mPFC following chronic drug use would cause related to the abnormal behavior in addicts including impulse and emotional changes. In the present study of a series of experiments, we used functional magnetic resonance imaging to examine the hemodynamic response of the mPFC and related circuits to various cognitive and emotional stimuli in heroin addicts and to explore the underlying dopamine neuromechnism by microinjection of tool drugs into the mPFC in laboratory animals. In the first experiment, we found that heroin patients, relative to the normal controls, took a much shorter time and committed more errors in completing the more demanding of cognitive regulation in the reverse condition of the task, while the neural activity in anterior cingulate cortex (ACC) was attenuated. In the second experiment, the scores of the heroin patients in self-rating depression scale (SDS) and Self-rating anxiety scale (SAS) were significantly higher than the normal controls and they rated the negative pictures more aversive than the normal controls. Being congruent with the behavioral results, hemodynamic response to negative pictures showed significant difference between the two groups in bilateral ventral mPFC (VMPFC), amygdala, and right thalamus. The VMPFC of patients showed increased activation than normal controls, whereas activation in the amygdala of patients was weaker than that in normal subjects. Our third experiment showed that microinjection of D1 receptor agonist SKF38393 into the mPFC of rats decreased hyperactivity, which was induced by morphine injection, in contrast, D1 receptor antagonist SCH23390 increased the hyperactivity, These findings suggest: (1) The behavior and neural activity in ACC of addicts changed in chronic drug users. Their impulsive behavior might result from the abnormal neural activity in the mPFC especially the ACC. (2) Heroine patients were more depress and anxiety than normal controls. The dysfunction of the mPFC---amygdala circuit of heroine addicts might be related to the abnormal emotion response. (3) Dopamine in the mPFC has an inhibitory effect on morphine induced behavior. The hyperactivity induced by chronic morphine was reduced by dopamine increase with D1 receptor agonist, confirm the first experiment that the neuroadaption of mPFC system induced by chronic morphine administration appears to be the substrate the impulse behavior of drug users.