Mosquito (Diptera: Culicidae) fauna in inland areas of south-west Western Australia

Abstract  Previously existing sources of data regarding mosquitoes in inland areas of south-west Western Australia are few and qualitative in nature. This is the first attempt to quantitatively investigate mosquito fauna in this region. The existing data are reviewed and compared with the results of the quantitative surveys presented in this paper. Temporal comparisons appear to indicate that mosquito community structure in the region may have changed since the initial surveys in the 1950s from a combination of freshwater-breeding species towards a strong dominance of Aedes camptorhynchus (Thomson), a major vector of Ross River virus in southern Australia. It is speculated that this shift may have been brought about by the increasing area and severity of dryland salinity in the region over the last century, and also may increase the potential for Ross River virus disease transmission.     

P2X7 receptor mediated phosphorylation of p38MAP kinase in the hippocampus

This study was designed to explore the effect of P2X7 receptor (P2X7R) activation on the expression of p38 MAP kinase (p38 MAPK) enzyme in hippocampal slices of wild-type (WT) and P2X7R^−/− mice using the Western blot technique and to clarify its role in P2X7 receptor mediated [³H]glutamate release. ATP (1 mM) and the P2X7R agonist BzATP (100 μM) significantly increased p38 MAPK phosphorylation in WT mice, and these effects were absent in the hippocampal slices of P2X7R^−/− mice. Both ATP- and BzATP-induced p38 MAPK phosphorylations were sensitive to the p38 MAP kinase inhibitor, SB203580 (1 μM). ATP elicited [³H]glutamate release from hippocampal slices, which was significantly attenuated by SB203580 (1 μM) but not by the extracellular signal-regulated kinase (ERK1/2) inhibitor, PD098095 (10 μM). Consequently, we suggest that P2X7Rs and p38 MAPK are involved in the stimulatory effect of ATP on glutamate release in the hippocampal slices of WT mice.     

水稻病程相关蛋白质在逆境胁迫下的表达研究

植物病程相关(PR)基因一般在病原物侵染过程中受诱导发生转录上调．目前有证据提示植物PR基因在非生物逆境胁迫下也发生转录变化,但其蛋白质的表达变化情况还鲜有报道．为了解水稻PR蛋白质在逆境胁迫下的表达特征,本文采用免疫印迹技术(Western blotting,WB)调查了8个PR蛋白质在冷、热、旱、淹和盐等5种胁迫下的表达谱．结果表明：在冷胁迫下PR8表达上调,在热胁迫下PR1a、PR3、PR5和PR16表达下调;在旱胁迫下PR1a、PR2和PR8表达上调,而PR5 和PR16表达下调,在淹胁迫下PR1、PR2和PR15表达上调,PR1a、PR3、PR5和PR8表达下调;在盐胁迫下PR2和PR3表达上调,而PR1a、PR5、PR8和PR16表达下调．另外,对这些PR 基因的上游启动子区进行分析,发现存在与胁迫响应相关的调控元件,其中脱落酸反应元件(ABRE)、TC-rich repeats和HSE的出现频率较高．这些蛋白质表达数据进一步佐证了PR蛋白在逆境胁迫反应中发挥着重要且不尽相同的作用．     

Preparation and Identification of Antidecapeptides of Subunit IV of Cytochrome b6-f Complex from Chloroplasts

Three synthetic decapeptides of subunit Ⅳ of cytochrome b6-f complex were coulpled respectively with ovalumine and purified using High-Performance Liquid Chromatography. They were served as antigens and injected into rabbits. Five weeks later, three kinds of monoclonal antibodies were obtained. Western blotting showed that there were immunoaffinity reactions between anti 17 kD-1, anti 17 kD-2, anti 17 kD-3 and 17kD band of cytochrome b6-f complex from spinach chloroplasts. Enzyme-linked immunosorbent assay showed that there were immunoaffinity reactions between anti 17 kD-1, anti 17 kD-2, anti 17 kD-3 and thylakoid membranes from spinach chloroplasts. Therefore, these antibodies can be used as probes to survey the location and orientation of 17 kD on the two sides of thylakoid membranes.     

鄂西青少年体质发育初步研究

目前,研究青少年体质发育的方法较多,作者试图用逐步回归分析法对此作些研究。 按照我国正常儿童青少年体格发育调查研究实施方案(儿童体格发育调查研究工作学习班,1976)和活体测量方法(黄新美,1983)的有关规定,对鄂西7—17岁的1533名青少年(男863人,女670人)进行了直接测量:1.身高;2.体重;3.上肢长;4.下肢长(由地面至大转子尖的距离)(靳仕信,1981);5.上半身长(身高—下肢长);6.上半身长与下肢长的比值。以上各项均值和标准差见表1.另外,还计算了下肢长指数（下肢长/身高×100）和上半身长指数（上半身长/身高×100）。将以上数据按性别、年龄逐个输入AppleII电子计算机（Basic语言）,对数据进行分析处理,用回归分析法（上海第二医学院数学教研室,1979;杨树勤,1985）分析青少年体重的变化与年龄、身高等七个因素的相关关系（见表2）,并对已进入方程式中的各项指标进行反复检查,最后,建立了推算青少年体重变化与年龄、身高的多元回归方程。     

鄂西地区裸藻的初步研究

在鄂西的五峰、宜都、宜昌、当阳及神农架林区一带,采集到裸藻门植物16属140种(包括变种和变型)。属于绿色裸藻类的有116种,无色裸藻类的有24种,其中有5个新种,7个新变种,3个新变型,有20种是我国新记录。在采集区域内的地形大体上可以分成三种不同的类型,即:山岳地区(采得裸藻5种),河谷盆地地区(采得裸藻40种)和沿长江丘陵地区(采得裸藻128种)。静止水体由于地形的差异,体积的大小和水质的肥沃程度不同,都对裸藻门植物的生长有重要的影响。       

Alpha diversity of lianas in a tropical evergreen forest in the Anamalais, Western Ghats, India

Abstract. Species richness, abundance, size-class distribution, climbing mode and spatial patterns of lianas were investigated in a 30-ha permanent plot of tropical evergreen forest at Varagalaiar in the Anamalais, Western Ghats, India. Each hectare was subdivided into 10 m × 10 m quadrats, in which all lianas ≥ 1 cm d.b.h. were measured, tagged and identified. The total liana density was 11, 200 individuals (373 ha–1) and species richness was 75 species, representing 66 genera and 37 families. The richness estimators employed for species and family accumulation curves after 100 times randomization of sample order, have stabilized the curves at 16th and 15th hectares, respectively. A greater proportion of lianas was twiners (55% of species and 44.4% of density) and root climbers (5% of species and 14% of density), and a few were tendril climbers, reflecting the late successional stage of the forest. In the size-class distribution, 82% of abundance and 97% of species richness fell within 1–3 cm diameter threshold. The dominance of succulent diaspore type signifies the faunal dependence of lianas on vertebrate frugivores for dispersal. The diversity, population density and family composition of lianas of our site is compared with those of other tropical forests. The need for biomonitoring of this synusia in the permanent plot for forest functioning is emphasized.     

家蚕生殖细胞相关基因nanos的克隆表达及在胚胎发育中的表达模式

【目的】探讨nanos基因在家蚕Bombyx mori胚胎发育中的表达模式,为进一步研究该基因在家蚕胚胎发育中的功能奠定基础。【方法】根据本实验室提交到GenBank中家蚕nanos的cDNA序列(登录号EF647589)设计引物,扩增出了一条长684 bp的编码片段,对该片段进行了克隆和表达,亲和纯化表达的蛋白并免疫新西兰大白兔制备抗体。Western blot检测家蚕早期胚胎nanos的表达情况,荧光定量PCR检测nanos在整个家蚕胚胎发育中的表达情况。【结果】克隆并表达了一条长684 bp的编码片段,得到了分子量约33 kD的融合蛋白。用制备的抗血清对家蚕早期胚胎蛋白的Western blot检测表明,nanos在此阶段基本是恒定表达。荧光定量PCR结果显示刚产的卵中nanos的表达量最大,第2天开始急剧下降,此后到第10天表达量几乎没有变化。【结论】本实验克隆的nanos是家蚕中的一个同源物,该基因在家蚕胚胎发育中的表达模式与蜜蜂等有很大的不同,反映了昆虫生殖细胞形成机制的多样性。     

脊神经节感觉神经35kD特异蛋白的纯化

为纯化和鉴定感觉神经特异蛋白,以兔脊髓背根神经节及背根纤维组织为材料,通过制备匀浆、离子交换层析 Ｄ Ｅ Ａ Ｅ Ｓｅｐｈａｃｅｌ,高压液相凝胶过滤层析分离纯化了脊神经感觉神经元 ３５ ｋ Ｄ蛋白,将其作为抗原制备抗 ３５ ｋ Ｄ 多克隆抗体． Ｗ ｅｓｔｅｒｎ ｂｌｏｔ 的结果表明,该蛋白特异地存在于脊感觉神经而不存在于脊运动神经．并初步观察到它对鸡胚背根节有神经营养作用．