Polymorphonuclear leukocyte migration through human amnion membrane

A new in vitro model has been developed for studying migration of human polymorphonuclear leukocytes (PMN) through living native cellular and matrix barriers. Human amnion membrane consists of a single layer of epithelium bound to a continuous basement membrane interfacing an avascular collagenous stroma. Living amnion was placed in plastic chambers with separate compartments on each side of the membrane. PMN were introduced on the epithelial side of the amnion, and a Millipore filter (Millipore Corp., Bedford, Mass.) was placed against the stromal side. In response to N-formylmethionyl-leucyl- phenylanlanine (FMLP) chemoattractant, PMN penetrated the full thickness of the amnion and were collected and counted on the filter. The rate of PMN traversal of the amnion was dependent on the concentration of FMLP (optimal at 10(-8)M) as well as the slope of the FMLP gradient across the amnion. The route of PMN migration was studied by transmission electron microscopy. PMN first attached to the epithelial surface, then infiltrated between intercellular junctions. PMN migrated around or through tight junction and hemidesmosome attachments. The PMN then penetrated the basement membrane and migrated through the dense collagenous stroma. The present amnion migration system has characteristics of the in vivo inflammatory state not described in any previous method for monitoring PMN migration in vitro. Prior methods have not used native epithelium, whole basement membrane, or collagenous stroma. PMN penetration of these barriers occurs in the normal inflammatory response and probably involves biochemical mechanisms not required for simple migration through the pores of an artificial filter. The amnion system can be useful for future biochemical and morphological studies of PMN penetration of these barriers and possible repair processes that may follow.     

Oxygen consumption rate of tissue measured by a micropolarographic method

A new method for measuring the oxygen consumption rate of a sheet of homogeneous tissue is described. The method measures, by a Clark-type oxygen electrode without a membrane, the time for the tissue to consume all its dissolved oxygen. The electrode is applied to one surface of the tissue sheet and the other surface is sealed from the atmosphere by a cover slip. The consumption is calculated from an estimate of the oxygen dissolved in the tissue at the moment it is covered and the time for the oxygen tension at one surface to fall to zero. The data also yield the oxygen diffusion coefficient in the oxygen-consuming tissue.     

厦门市海岸带水污染负荷估算及预测

综合采用灰色模型、曲线回归等预测方法,建立了基于厦门市海岸带特征的主要污染源水污染负荷估算及预测模型,并采用厦门市历年统计数据对模型加以验证.对厦门市近岸海域近10年的废水和主要污染物质排放量估算的结果表明:万元产值工业废水排放量呈逐年下降的趋势,而各污染物的排放总量却逐年缓慢增长;在点源污水排放总量预测中,约76%的氮、磷来自于生活污水;在非点源污染负荷中,农业非点源中的氮、磷负荷占较大比例,城市非点源污染负荷比例最小.2005年厦门海岸带各污染源产生的氮污染负荷大小比较结果为:生活污染源>农业非点源>工业污染源>旅游业污染源>城市非点源,磷污染负荷则为:农业非点源>生活污染源>工业污染源>旅游业污染源>城市非点源.     

First record of lily thrips, Liothrips vaneeckei Priesner, in Australia (Thysanoptera: Phlaeothripidae)

The first Australian record of the lily thrips, Liothrips vaneeckei Priesner, is reported from a bulb farm in Warragul South, Victoria. It is an occasional pest of Lilium bulbs, both in the field and in storage, particularly in the USA and several European countries, and is also infrequently found in considerable numbers on the corms of orchids.     

Bulbing in Long-day Onion (Allium cepa L.) Cultured In Vitro: Comparison Between Sugar Feeding and Light Induction

Bulbs were obtained on onion plants cultured in vitro. No bulbinghappened under long days with fluorescent light and 30–40g l^–1 sucrose. Bulb formation was mainly dependent eitheron sucrose concentration in the culture medium, or on lightspectral composition. Raising the sucrose concentration from40 to 120 g l^–1 increased plant basal swelling and stoppedfurther vegetative development. These plants were not dormant.When fluorescent light was enriched in incandescence duringa long day period, bulbs were obtained in two months and underwenta consecutive dormancy. Bulb, dormancy, light spectral quality, photoperiod, R: FR ratio, sugar, tissue culture