800 resultados para Drug Use Patterns


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为更好地掌握黄土丘陵区不同土地利用方式下的土壤水分入渗性能,采用双环法和人工降雨法,分别对陕西省延安市燕沟流域林地、草地、农地3种土地利用方式的土壤水分入渗过程进行了对比试验。结果表明:双环法能较好的反映水向土中的入渗过程;而人工降雨法可以较为真实地反映天然降雨过程中雨水向土中的入渗过程, 两者有很大的不同,主要表现在土壤水分的入渗速率变化过程方面。前者测定的土壤水分入渗速率主要受制于土壤的物理性状,而后者:不但与土壤物理性状有关,还与降雨强度有较密切的关系。在人工模拟短历时暴雨条件下, 对于林地和荒坡草地,土壤水分入渗速率有随雨强增大而增大的趋势,而对于裸耕农地,随着雨强的增大,土壤水分入渗速率有降低的趋势。

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对黄土丘陵沟壑地区不同土地利用模式土壤酶活性和土壤微生物进行了测定,研究了土壤酶活性、微生物与土壤主要肥力指标对黄土丘陵沟壑地区不同土地利用模式下土壤肥力质量的关系。结果表明,不同土地利用模式0~20 cm土壤酶活性之间差异明显,而20~40 cm不同土地利用模式之间土壤酶活性差异较小,研究区域不同土地利用模式土壤微生物数量差距较大。本研究利用因子分析法来分析不同土地利用方式土壤酶活性、土壤微生物数量和土壤主要肥力指标,并根据各因子之间综合得分得出:日光温室的土壤肥力效益最好,然后依次为农田、拱棚、经济作物、果园。

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采用野外调查和室内分析的方式对子午岭不同土地利用方式下,土壤有机质、3种活性有机质及其碳库管理指数(CMI)进行了研究,结果表明,土壤有机质、3种活性土壤有机质含量均随土层的加深逐渐降低,在土壤剖面基本表现为林地、撂荒未翻耕地>撂荒翻耕地>农用地.同一土层,3种土壤活性有机质含量及其有效率表现为低活性有机质>中活性有机质>高活性有机质.不同利用方式下,活性有机质有效率随有机质活性增强,呈现撂荒未翻耕地>林地>撂荒翻耕地>农用地的趋势.不同利用方式之间的CMI的差异随有机质活性的增强而增大,且影响深度也逐渐加深.在0~30cm土层内,林地3种活性有机质的CMI高于撂荒翻耕地和农用地;而在30cm之下土层,3种利用方式低活性有机质的CMI相差不大,但中活性有机质和高活性有机质的CMI表现为林地>撂荒翻耕地>农用地.3种活性土壤有机质与其他生物化学性质之间均表现为显著或极显著相关关系,表明活性有机质可以指示土地利用方式对土壤有机质和CMI的影响.

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water wind erosion crisscross region; soil respiration rate; seasonal changes; land use pattern; soil temperature; soil moisture; 【摘要】 以黄土高原水蚀风蚀交错区神木县六道沟小流域为研究区,采用动态密闭气室法对植物生长季节(2007年5~10月)5种土地利用方式的土壤呼吸速率进行了测定,并结合水热因子,对不同土地利用方式间土壤呼吸速率的差异性以及其和温度、含水量之间的关系进行了分析。结果表明:5种土地利用类型土壤呼吸速率季节性变化均呈现单峰型曲线,与气温变化趋势一致,其7、8月份土壤呼吸速率均显著高于其它月份(P<0.05);生长季节土壤CO2平均释放速率顺序为:长芒草地>苜蓿地>柠条地>农地>沙柳地,草地在生长前期和旺盛期土壤呼吸强度均显著高于农地和灌木林地;除沙柳地和苜蓿地以外,在土壤呼吸与所有温度指标的关系中,与10cm深度的土壤温度相关性最好,且除沙柳地外,其它4种土地利用类型均与之达到显著相关;农地土壤呼吸对温度的响应最敏感(Q10值为2.20),除沙柳地(Q10值为1.48)外,其它4种土地利用类型Q10值均在2.0左右,接近于全球Q10的平均水平;通过Van’t Hoff模型估算,2007年植物整个生长季节(5~10月份),5种土地利用类型土壤呼吸量从高到低依次为:苜蓿地259gC·m-2,长芒草地236gC·m-2,柠条地226...

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以中国科学院沈阳生态试验站的长期定位试验为平台,测定并分析了下辽河平原不同土地利用方式下潮棕壤的微生物生物量、基因多样性和群落结构。结果表明,不同土地利用方式会对土壤微生物特性产生影响: 氯仿熏蒸法测定土壤微生物生物量结果显示,裸地处理的微生物生物量碳、氮较低,割草和休闲地则显著高于其它处理。在农田生态系统中,长期单施循环猪圈肥显著提高了土壤微生物生物量碳、氮,而长期单施NPK肥处理与CK相比则略有降低,在施用化肥基础上配合养分循环再利用,微生物生物量碳、氮介于CK和单施循环猪圈肥之间。 PCR-DGGE图谱显示,处理间细菌条带分布较相似,其中裸地处理细菌多样性最高;长期土地利用格局改变了土壤真菌群落结构,施肥增加了真菌多样性,且有机肥的影响大于化肥;不同处理间氨氧化细菌群落结构差异明显,NPK+M处理明显增加了氨氧化细菌多样性,且无机肥和有机肥对氨氧化细菌影响不同。土地利用方式对细菌影响较小,但明显改变了真菌和氨氧化细菌的群落结构。聚类分析结果显示,撂荒和割草处理较施肥对细菌、真菌和氨氧化细菌多样性的影响更明显。 PLFA测定的细菌脂肪酸和真菌脂肪酸与总微生物量变化规律相似,均为:休闲和割草处理最高,农田次之,裸地最低;农田处理间PLFA含量差异较小,其中M处理最高,其次为CK和NPK+M处理,NPK处理最低;撂荒和施用有机肥提高了微生物PLFA量,而施用化肥则降低了微生物PLFA量;自然生态系统中土壤具有较高的G+/G-;休闲和割草处理具有较低的细菌/真菌,农田生态系统和裸地的细菌/真菌则较高;PLFA与土壤养分相关性分析表明, PLFA量与土壤有机质和总氮显著相关。PLFA表征的微生物生物量呈现春秋略低,夏季略高的趋势。 不同的测定方法从不同角度分析了微生物特性,氯仿熏蒸法和PLFA方法之间存在很好的相关性,微生物生物量和多样性之间相关性比较弱。

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利用SWAP(Soil-Water-Atmosphere-Plant)模型对黄土高原水蚀风蚀交错区坡地土壤-植被-大气系统中的水循环进行数值模拟。结果显示,SWAP模型很好的模拟了不同土地利用方式条件下的土壤水循环过程。根据模拟结果,水蚀风蚀交错区的丰水年份,农地和种植第一年的紫花苜蓿地季末土壤水分稍有盈余,谷子和紫花苜蓿的日蒸散量分别为1.2~2.6 mm和1.2~2.5 mm。

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通过对苹果地、农田和其他塬面主要土地利用方式的比较研究 ,发现苹果地土壤入渗速率大、降雨产流率低和存在生物利用型土壤干层。这些水文学性质将增强土壤 -植物 -大气间垂直水分交换 ,削弱降雨转化为地表径流和地下水的比例 ,最终影响区域地表和地下水资源的数量。另外土壤干层的出现还削弱了土壤水库对年际和季节性干旱的调节作用 ,导致苹果产量随降雨量的自然变化呈现较大波动

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Behavioral and functional imaging studies consistently show that heroin abuse leads to various cognitive impairments, while brain structural changes associated with heroin use remain poorly understood. In the current study, we used voxel-based morphology (VBM), a method sensitive to structural changes of the brain, to investigate the gray concentration in MRI structure images of heroin addicts. Results show that the concentration of the temporal cortex and frontal cortex of heroin users significantly decreased as compared to age/education matched normal controls. Further analysis revealed that this brain structure change was detectable only in the users who had used heroin more than 5 year, but not in the remaining users. These results converge to the abnormality of the brain structure in heroin users and this abnormality is clearly associated with duration of drug use. We then analyzed the large-scale brain structure network in the heroin addicts. As compared to the normal controls, there was significant difference in interregional correlation between the temporal cortex, hippocampus, thalamus, and frontal cortex. Importantly, two major indices of the small-world properties, Clustering coefficient(Cp) and shortest path length (Lp), which are thought to reflect the local specialty and global integrity, were marginal-significantly larger than the normal controls, especially for Lp. These results suggest that chronic use of heroin results in the reorganization of the brain system. Taken together, this thesis has provided compelling evidence for brain structure impairments in chronic heroin users and further characterized the large-scale brain structure network in the same population.

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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.

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Rewarding experience after drug use is one of the mechanisms of substance abuse. Previous evidence indicated that rewarding experience was closely related to learning processes. Neuroscience studies have already established multiple-mode learning model. Reference memory system and habit memory are associated with hippocampus and dorsa striatum respectively, which are also involved in the rewarding effect of morphine. However, the relationship between spatial/habit learning and morphine reward property is still unclear. After drug use, with sensitization to rewarding effect, spatial learning is also changed. To study the mechanism of increment of spatial learning would provide new perspective about reward learning. Based on the individual difference between spatial learning and reward learning, the experiments studied relationship between the two leaning abilities and tested the function of dorsal hippocampus and dorsal striatum in morphine-induced CPP. The results were summarized below: 1 In a single-rule learning water maze task, subjects better in spatial learning also excelled in rewarding learning. In a multi-rule learning task, morphine administration was more rewarding to subjects of use place strategy. 2 Treatment potentiating the rewarding effect of morphine also increased place-rule learning, with no significant improvement in habit learning. 3 Intracranial injections into CA1 of hippocampus or dorsal striatum of M1 antagonist, Pirenzepine, could block the establishment of morphine CPP after three days morphine treatment. In contrast, the antagonist of D1 receptor SCH23390 had no blocking effect. Both Pirenzepine and SCH23390 blocked the locomotor-stimulating effect of morphine. In summary, spatial learning stimulated the behavioral expression of morphine’s rewarding effect, in which CA1 of hippocampus was critically involved. On the other side, a pretreatment schedule of morphine, while increased the rewarding effect, improved place-rule learning, indicating that spatial learning might be one chain of sensitization to drug rewards effects

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That relapse still exists even after prolonged withdrawal is a difficult issue in the medical cure of drug addiction. Neuro-adaptation induced by prolonged exposure to addictive drugs is the neural mechanisms of both compulsive drug seeking and relapse.Neuro-adaptation caused by addictive drugs increases the individuals’ response to drugs and on the other hand, it reduces the response to natural reward in withdrawn individuals.There must be common neural mechanisms between the co-existing phenomena, and there must also be unique neural mechanisms in the drugs.To reveal the neuro-adaptation arising in the process from random, controllable drug-use to uncontrollable compulsive drug seeking is of great significance both theoretically and practically.Based on the above hypothesis, in order to reveal the function of alpha adrenergic receptor in compulsive drug-seeking motivation during the process of drug addiction, using sensitization of morphine-induced psychomotor activity as behavioral model, through the method of behavioral pharmacology, the neural mechanisms of alpha adrenergic receptor’s involvement in the process of addiction has been studied.The adjustment function caused by alpha receptors in medial prefrontal cortex and nucleus accumbens to morphine-induced psychomotor activity has been compared in the period of first use of drugs and in repetitive-use period. Furthermore, the effect on novelty seeking caused by alpha-receptors in relevant brain areas has also been compared. Major results are as follow: 1 After prolonged morphine exposure, rats’ response to morphine-induced psychomotor activity is strengthened and response to novel object induced reward weakened. 2 Injection of prazosin in medial prefrontal cortex will block morphine-induced psychomotor activity of naïve rats, however, it will not block that of morphine-withdrawn rats, but it will block the novelty seeking behavior of morphine-withdrawn rats. 3 Injection of clonidine in medial prefrontal cortex will block morphine-induced psychomotor effect of both naïve rats and morphine-withdrawn rats, and will block the novelty seeking behavior of morphine-withdrawn rats. 4 Injection of prazosin in nucleus accumbens will not affect the morphine-induced psychomotor effect of either naïve rats or morphine-withdrawn rats, nor will it affect the novelty seeking behavior of morphine-withdrawn rats. 5 Injection of clonidine in nucleus accumbens will block morphine-induced psychomotor effect of naïve rats, however, it will not block that of morphine-withdrawn rats, nor will it affect the novelty seeking behavior of morphine-withdrawn rats. These results show: 1 The weakening of the function of alpha1 receptors in medial prefrontal cortex and alpha2 receptors in nucleus accumbens caused by repetitive exposure to morphine is probably the cause of compulsive drug-seeking activity. 2 Blocking alpha1 receptors in medial prefrontal cortex accelerates the loss of interest in natural reward after morphine withdrawal. 3 Blocking alpha2 receptors in medial prefrontal cortex not only restrains drug-seeking motivation, but also blocks the individual’s seeking motivation for novelty stimulus, which suggests that, while selecting medicine for curing addiction, it should be considered to reduce the influence on natural reward as much as possible and to avoid major side-effect.

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In recent years, the deficit of inhibition has become an important reason for explaining addiction. Response inhibition resembles the compulsive drug seeking behavior and it is the basement of addiction inhibition deficits. However, there were no enough evidence for the relationship between addiction and response inhibition deficits and the results of the neuro mechanisms studies remains unclear. Few studies has focused on the exploring the heroin users. Among those paradigms for study response inhibition deficits, stop signal is a very suitable model for the representation of compulsive drug seeking, but only a few researches has worked on this paradigm. In this study, we selected about 100 heroin abusers and had behaviour and neuro imaging scannings for investigating the response inhibition deficits. The behaviour researches found: first, the chronic heroin users had longer reaction time than control group and this reaction time were not affected by stop signals in heroin users. Second, heroin users had less waiting time than control group and they were more impulsive but less flexibility. Their erro monitoring and flexibale adjustment ability decreased. Third, the SSRT of heroin users was significantly longer than control group. These results suggested that the inhibition of heroin users were impaired. Further investigation showed that the SSRT of heroin users had positive correlation of four factor scores of ASI and the macro correlation coefficient was factor three of drug use. This correlation suggested that drug use was the main reason of inhibition deficits. fMRI results mainly focused on the ANOVA analysis for group difference. First, there was no intensity difference in M1 and SMA brain areas between the two groups. Second, heroin users had less activation in right dorsalateral prefrontal cortex, right inferior prefrontal cortex and anterior cingulated cortex, while in bilateral striatum and amygdala, heroin users had more activation than control group. The right prefrontal cortex was indentified as the main inhibition brain area. The anterior cingulated cortex has relationship with erro monitoring and amygdale was an important brain area for impulsivity and emotion control. The network of these brain areas was envovled in impulsivity and inhibition and it was suggested the mainly damaged network for heroin users’ disinhibition. We also investigated the gray matter changes of heroin users and found that chonic heroin use made their gray matter density decreased in prefrontal cortex (including bilateral dorsalateral prefrontal cortex, obital frontal cortex, inferior prefrontal cortex) and anterior cingulated cortex. The gray matter density in these brain regions had negative correlation with drug use duration. In conclusion, we indentified the disinhibition of heroin users and its neuro mechanism. Their compulsivity brain areas had more activation than control group and their inhibition brain areas had less activation than normal control. On the other side, the biological mechanism of this activation changes was the gray matter density decrease in these brain areas.

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Durbin, J. & Urquhart, C. (2003). Qualitative evaluation of KA24 (Knowledge Access 24). Aberystwyth: Department of Information Studies, University of Wales Aberystwyth. Sponsorship: Knowledge Access 24 (NHS)

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Dissertação de Mestrado apresentada à Universidade Fernando Pessoa como parte dos requisitos para obtenção do grau de Mestre em Psicologia da Educação e Intervenção Comunitária.

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Background: Deliberate self-harm (DSH) is common among adolescents in Ireland and internationally. Psychological factors, negative life events and lifestyle factors have been found to be associated with self-harm in this group. However, large scale population-based studies of adolescent selfharm and its correlates have been lacking, and internationally a standardised methodology was needed to facilitate comparative studies. The focus on vulnerability which has been prevalent in this field has meant that research has failed to examine resilient adaptation among at-risk adolescents. Method: Data were obtained from a cross-sectional school-based study conducted in Ireland and in each of the six other centres which participated in the Child and Adolescent Self-harm in Europe (CASE) study. In Ireland, 3,881 adolescents in 39 schools in completing the anonymous questionnaire, while across all 7 centres, over 30,000 young people participated. Data were gathered on health and lifestyle, self-harm thoughts and behaviour, a wide range of life events, psychological characteristics (anxiety and depressive symptoms, self-esteem, impulsivity and coping style), and support available to young people. Results: This thesis reports the findings of the Irish CASE centre as well as one international study. The factors associated with DSH among Irish adolescents differed by gender, but among both genders drug use and knowing a friend who had engaged in self-harm were associated with DSH. Among Irish boys, strong associations were found between bullying and poor mental health and DSH. Among boys who had been bullied, psychological and school factors were associated with DSH, while family support was protective. Links between stressful life events, psychological characteristics and DSH within the international CASE sample were examined. Increased history of self-harm thoughts and acts was associated with greater depression, anxiety and impulsivity, lower self esteem and an increased prevalence of ten different negative life events, supporting the hypothesis of a “dose-response” relationship between these risk factors and the self-harm process. Associations between coping style, mental health factors (depressive symptoms, anxiety and self-esteem) and self-harm were examined among Irish adolescents. Emotion-oriented coping was strongly associated with poorer mental health and self-harm thoughts and acts. A mediating effect of emotion-oriented coping on associations between mental health factors and DSH was found for both genders and between problem-oriented coping and mental health factors for girls. Similar mediating effects of coping style were found when risk of self-harm thoughts was examined. Resilient adaptation among adolescents exposed to suicidal behaviour of others was examined. Self-harm thoughts were common in these adolescents. Among those exposed to suicidal behaviour of others, vulnerability factors were drug use and higher levels of anxiety among boys, while for girls drug use, bullying and abuse were vulnerability factors, while resilience was associated with higher self-esteem and use of problem-oriented coping. Conclusion: These findings can aid in the identification of young people at risk of self-harm in the school setting and highlight the importance of mental health, peer-related and lifestyle factors in the development of DSH. High-risk groups of young people such as bullying victims and those exposed to suicidal behaviour of others have distinctive profiles of risk factors which differ from those of their peers. Findings relating to the importance of positive coping skills can inform positive mental health programmes, many of which aim to enhance life skills and build resilience among young people. Knowledge of the factors associated with positive adaptation among at-risk adolescents can inform prevention efforts among this group.