浙江省中部萤石产区氟环境与地方性氟病

通过对浙江省中部萤石产区氟地球化学环境的初步研究，探讨了该区地方性氟病的成因和分布规律，指出了地方性氟病与高氟环境的关系。     

水体中隐孢子虫卵囊的检出及其活力分析

从水中检测隐孢子虫卵囊是评价水源传播人类隐孢子虫病风险的第一步，从水中检出的卵囊的活力需要进行测定才能估计水源爆发的真正风险，应用聚丙烯盒式过滤器和美国环保局（USEPA）1622过滤方法的囊式过滤器（Gelman,Michigan,USA)，分别过滤了当地（法国鲁昂）的环境水和供给水，并用免疫磁分离技术（IMS）进行分离。用免疫荧光检测法（IFA）从浓缩的水样中检测到了隐孢子虫卵囊。环境水中的卵囊浓度是每升水中0.12-2.7个卵囊；供给水中的卵囊浓度是每升水中0.03-0.06个卵囊，用新生小鼠模型初步评价了检出卵囊的感染力。结果证明了隐孢子虫卵囊在环境中尤其是水中的广泛分布；同时表明，评估水源传播的隐孢子虫病的风险时，不仅要从水中检出卵囊，而且要测定检出的卵囊的活力。表1参22。     

湘黄鸡马立克氏病(MD)临床免疫方法及效果研究

通过本次临床试验得出；湘黄鸡马立克氏病(MD)的免疫以CVI988 HVT苗或Rispens CVI988苗为最佳效果，可使该病的临床发病率分别控制在1．33％和1．67％以下，致瘤率为34％左右．用中药进行预防达不到免疫的效果．所以认为用血清I型疫苗是目前衡阳地区湘黄鸡马立克氏病(MD)的唯一有效的免疫方法．     

白兰瓜果腐病病原菌的分离鉴定及优势病菌的毒性测定

对引起白兰瓜贮藏期果腐病的病原菌进行了分离、鉴定和致病性测定，明确了Fusarium lateritium Nees，Cephalothecium roseum，Aspergillus spp．，Penicillium spp．，Rhizopus stolonifer等5种引起白兰瓜果实腐烂的病原真菌，其中以F.lateritium Nees的危害最为严重，为优势菌，其次为C.roseum．而F.lateritium在pH6的Richard培养液中，置25℃黑暗静置培养14d后获得的培养滤液对白兰瓜种子胚根的抑制率最强．F.lateritium产生的毒素为非专化性毒素．表4参7     

黄河循化—贵南段两种地方病与水文地质环境的关系初探

黄河上游两岸广泛分布着甲状腺肿与地方性氟病,经过调查分析,这两种地方病是在特定的水文地质环境中形成的,合理利用地下水是解决这两种地方病的有效途径     

人体需要经常补硒

从硒的生物学作用和防治疾病等方面剖析了硒与人体健康的关系；从元素地球化学、生物地球化学和化学地理等方面探讨了我国缺硒区的形成、分布和等级的划分；从环境地球化学物质场和元素生物地球化学营养链等方面．阐明了作物、禽畜和人体缺硒的原因、危害及其人体补硒的途径和方法，提出了在缺硒区运用元素生物地球化学营养链营养结构模式的原理、和技术方法，从土壤中获取富硒有机食品，供居民食用，是进行食物补硒、提高人体摄硒量、提高人体免疫功能和防治缺硒病症的根本措施。     

常规水处理厂中小隐孢子虫卵囊的去除效果

介绍了小隐孢子虫卵囊的特点及其对人体的危害，分析了pH、混凝剂种类与投加量、电导率和天然有机物含量等对小隐孢子虫卵囊的Zeta电位的影响，总结了混凝－沉淀－过滤和直接过滤对小隐孢子虫卵囊的去除效果，探讨了水温、水质、混凝剂种类与投加量、滤料层组成和滤速等对去除效果的影响。     

大连太平洋牡蛎体内寄生虫:沿岸单孢子虫检测

于2007年3月,采集大连大窑湾浮筏贝类养殖区的太平洋牡蛎,抽取牡蛎的血淋巴液进行沿岸单孢子虫的研究。采用显微镜观察、聚合酶链式反应(PCR)和原位杂交(ISH)方法对血淋巴液样品进行检测。结果在显微镜下观察到牡蛎血淋巴液中存在沿岸单孢子虫(Haplosporidium costale,SSO)原生质体的类似物;提取血淋巴液基因组DNA,应用扩增沿岸单孢子虫SSUrDNA区域的引物对进行PCR扩增,产生约150bp的基因片段,经测序并将测序结果与基因库中已知序列比对分析,确定这种类似物为沿岸单孢子虫。同时,采用沿岸单孢子虫的特异性DNA探针SSO1318,对牡蛎血淋巴液中的沿岸单孢子虫进行原位杂交,结果为阳性。     

Using the nematode Caenorhabditis elegans as a model animal for assessing the toxicity induced by microcystin-LR

Among more than 75 variants of microcystin(MC),microcystin-LR(MC-LR) is one of the most common toxins.In this study,the feasibility of using Caenorhabditis elegans to evaluate MC-LR toxicity was studied.C.elegans was treated with MC-LR at different concentrations ranging from 0.1 to 80 μg/L.The results showed that MC-LR could reduce lifespan,delay development,lengthen generation time,decrease brood size,suppress locomotion behavior,and decreases hsp-16-2-gfp expression.The endpoints of generation time,brood...     

Induction of chemotaxis to sodium chloride and diacetyl and thermotaxis defects by microcystin-LR exposure in nematode Caenorhabditis elegans

Apart from the liver disruption, embryotoxicity and genotoxicity, microcystin (MC)-LR also could cause neurotoxicity. Nematode Caenorhabditis elegans was explored as a model to study the neurotoxicity. In the present study, we provided evidence to indicate the neurotoxicity on chemotaxis to NaCl and diacetyl, and thermotaxis from MC-LR exposure to C. elegans. As a result, higher concentrations of MC-LR caused significantly severe defects of chemotaxis to NaC1 and diacetyl, and thermotaxis. The neurotoxicity on chemotaxis to NaCl and diacetyl, and thennotaxis from MC-LR exposure might be largely mediated by the damage on the corresponding sensory neurons (ASE, AWA, and AFD) and interneuron AIY. The expression levels of che-1 and odr-7 were significantly decreased (P<0.01) in animals exposed to MC-LR at concentrations lower than 10 μg/L, whereas the expression levels of ttx-1 and ttx-3 could be significantly (P<0.01) lowered in animals even exposed to 1 μg/L of MC-LR. Moreover, both the chemotaxis to NaCl and diacetyl and the thermotaxis were more significantly reduced m MC-LR exposed mutants of che-1(p674), odr-7(ky4), ttx-1(p767), and ttx-3(ks5) than those in exposed wild-type N2 animals at the same concentrations.