Transfer, Perception, and Activity of Male Pheromone of Acrolepiopsis assectella with Special Reference to Conspecific Male Sexual Inhibition

In the leek moth, Acrolepiopsis assectella, the male, stimulated by a calling female, produces a sexual pheromone that is active on the female. The male-produced pheromone blend contains eight alkanes previously isolated from the male hair-pencils. We used EAG techniques to study the effect of the pheromone on females reared on leek or on artificial diet and on males reared on leek. The optimal stimulation duration appeared to be 1.6 sec exposure to the pheromone or components. The concentrations tested on the antenna were of the order of 10¹² molecules/cm³. The hair-pencil extract tested was of an estimated concentration of around 10⁹ molecules/cm³. The antennal responses are expressed relative to responses to a standard, amyl acetate, but also as an absolute value. Generally, females reared on artificial diet and males reared on leek responded better than females reared on leek. Of the alkanes tested, those present in hair-pencils gave higher responses, with hexadecane always giving the strongest response. A possible inhibiting activity of male leek moth pheromone on the sexual behavior of conspecific males was investigated. The behavior of sexually stimulated males was observed in the presence of other males, hair-pencil extracts, and different compounds either pure or in a mixture. The experiments established that in this species, male pheromone inhibits wing fluttering duration of conspecific males. This inhibition was obtained not only with fluttering males as a source of pheromone but also with all the alkanes tested. The inhibition was due to hair-pencil chemicals, particularly if these were perceived by olfaction plus contact. Wing fluttering increased the inhibitory activity of male-derived alkanes.     

Study of an aramid surface reactivity: Modification with a cold plasma or an electron beam followed by a postgrafting reaction

Different modes of activation are described for a postgrafting reaction of acrylic acid on poly(p-phenylene terephthalamid) (PPTA)mitrogen plasma or electron-beam irradiation. Both lead to surface radical formation, and these species are able to initiate grafting. The Functionalization through amino group attachment is characteristic of plasma treatment. Degradation initiated by UV-visible emission of plasma is noticed, leading to the amide clivage. The surface grafting is more important when the PPTA is irradiated with a cold plasma and if water is used as the solvent. The polymer crystallinity degree reduces the grafting of the electron beam-irradiated PPTA even with a high radical concentration. © 1994 John Wiley & Sons, Inc.     

Correlation between activity and acidity on zeolites: a high temperature infrared study of adsorbed acetonitrile

The influence of the temperature on the protonation of acetonitrile by acidic zeolites was studied by infrared spectroscopy. Acidity at room or low temperature was not correlated with the protonation temperature, but the zeolitic structure played an important role. A new technique is presented for the study of the acidity of solids under reaction conditions. A good correlation was obtained in a series of various zeolites between the catalytic activity in the cracking of n-hexane and the protonation temperature of acetonitrile. This revised version was published online in June 2006 with corrections to the Cover Date.     

MIM零件烧结过程中收缩和变形的数值模拟

为描述金属粉末注射成形坯件在烧结过程中的收缩和变形行为,基于连续介质力学原理建立了符合粘塑性本构关系的宏观烧结模型。该模型通过有限元软件Abaqus的用户子程序实现,进行烧结过程的数值模拟。分析了由于坯件重力、非均匀初始密度分布以及坯件支承体之间的摩擦力等因素而引起的非均匀收缩和变形。通过与试验结果的比较,验证了烧结模型和数值方法的正确性。     

Invited article: the fast readout low noise camera as a versatile x-ray detector for time resolved dispersive extended x-ray absorption fine structure and diffraction studies of dynamic problems in materials science, chemistry, and catalysis

Originally conceived and developed at the European Synchrotron Radiation Facility (ESRF) as an "area" detector for rapid x-ray imaging studies, the fast readout low noise (FReLoN) detector of the ESRF [J.-C. Labiche, ESRF Newsletter 25, 41 (1996)] has been demonstrated to be a highly versatile and unique detector. Charge coupled device (CCD) cameras at present available on the public market offer either a high dynamic range or a high readout speed. A compromise between signal dynamic range and readout speed is always sought. The parameters of the commercial cameras can sometimes be tuned, in order to better fulfill the needs of specific experiments, but in general these cameras have a poor duty cycle (i.e., the signal integration time is much smaller than the readout time). In order to address scientific problems such as time resolved experiments at the ESRF, a FReLoN camera has been developed by the Instrument Support Group at ESRF. This camera is a low noise CCD camera that combines high dynamic range, high readout speed, accuracy, and improved duty cycle in a single image. In this paper, we show its application in a quasi-one-dimensional sense to dynamic problems in materials science, catalysis, and chemistry that require data acquisition on a time scale of milliseconds or a few tens of milliseconds. It is demonstrated that in this mode the FReLoN can be applied equally to the investigation of rapid changes in long range order (via diffraction) and local order (via energy dispersive extended x-ray absorption fine structure) and in situations of x-ray hardness and flux beyond the capacity of other detectors.     

Effect of watershed parameters on mercury distribution in different environmental compartments in the Mobile Alabama River Basin, USA

Total mercury (THg) and mono-methylmercury (MeHg) levels in water, sediment, and largemouth bass (LMB) (Micropterus salmoides) were investigated at 52 sites draining contrasting land use/land cover and habitat types within the Mobile Alabama River Basin (MARB). Aqueous THg was positively associated with iron-rich suspended particles and highest in catchments impacted by agriculture. Sediment THg was positively associated with sediment organic mater and iron content, with the highest levels observed in smaller catchments influenced by wetlands, followed by those impacted by agriculture or mixed forest, agriculture, and wetlands. The lowest sediment THg levels were observed in main river channels, except for reaches impacted by coal mining. Sediment MeHg levels were a positive function of sediment THg and organic matter and aqueous nutrient levels. The highest levels occurred in agricultural catchments and those impacted by elevated sulfate levels associated with coal mining. Aqueous MeHg concentrations in main river channels were as high as those in smaller catchments impacted by agriculture or wetlands, suggesting these areas were sources to rivers. Elevated Hg levels in some LMB were observed across all types of land use and land cover, but factors such as shallow water depth, larger wetland catchment surface area, low aqueous potassium levels, and higher Chl a concentrations were associated with higher Hg burdens, particularly in the Coastal Plain province. It is suggested that the observed large variability in LMB Hg burdens is linked to fish displacement by anglers, differences in food web structure, and sediment biogeochemistry, with surficial sediment iron oxides buffering the flux of MeHg from sediments to deeper water pelagic food webs.     

As(V) retention and As(III) simultaneous oxidation and removal on a MnO2-loaded polystyrene resin

Based on KMnO4 oxidative capacity, a polystyrene matrix loaded with manganese dioxide was synthesized from an anionic commercial resin in chloride form. This medium, called R-MnO2, was tested for As(V) retention and for As(III) simultaneous oxidation and removal. Equilibrium was reached in 2 h and isotherms showed that R-MnO2 maximal capacities towards As(III) and As(V) are, respectively, 0.7 and 0.3 mmol/g. Various mechanisms were involved in As(III) retention: oxidation of H3AsO3(0) by MnO2(s) leading to the formation of HAsO4(2)- and Mn2+, fixation of As(V) formed on the resin beads and precipitation of Mn3(AsO4)2 with Mn2+ released. Successive arsenic desorption and retention steps were performed and showed that the quantity desorbed was low compared to the quantity removed during the first stage of the process. A second removal step, carried out under the same conditions as the first one, proved that the matrix second-removal capacity was weak. This solid sorbent, although not reusable, can be considered in field application as arsenic retention is really strong.     

Cohesiveness and hydrodynamic properties of young drinking water biofilms

Drinking water biofilms are complex microbial systems mainly composed of clusters of different size and age. Atomic force microscopy (AFM) measurements were performed on 4, 8 and 12 weeks old biofilms in order to quantify the mechanical detachment shear stress of the clusters, to estimate the biofilm entanglement rate ξ. This AFM approach showed that the removal of the clusters occurred generally for mechanical shear stress of about 100 kPa only for clusters volumes greater than 200 μm³. This value appears 1000 times higher than hydrodynamic shear stress technically available meaning that the cleaning of pipe surfaces by water flushing remains always incomplete. To predict hydrodynamic detachment of biofilm clusters, a theoretical model has been developed regarding the averaging of elastic and viscous stresses in the cluster and by including the entanglement rate ξ. The results highlighted a slight increase of the detachment shear stress with age and also the dependence between the posting of clusters and their volume. Indeed, the experimental values of ξ allow predicting biofilm hydrodynamic detachment with same order of magnitude than was what reported in the literature. The apparent discrepancy between the mechanical and the hydrodynamic detachment is mainly due to the fact that AFM mechanical experiments are related to the clusters local properties whereas hydrodynamic measurements reflected the global properties of the whole biofilm.     

316L不锈钢粉末注射成形件的烧结致密化行为

为了控制粉末注射成形零件的最终尺寸精度和力学性能,对316L不锈钢粉末注射成形件的烧结致密化行为进行了试验研究,分析了烧结温度和升温速率对试件致密化行为以及烧结件力学性能的影响.试验结果表明,致密化过程始于1080℃左右,主要在1200～1300℃的升温过程中快速进行,致密化速率随着升温速率的升高而升高.烧结件的抗拉强度、抗弯强度以及延伸率,不但取决于致密化程度,而且与微观结构有关.分析表明,将基于扩散控制和强度控制的烧结理论结合,可以有效地解释316L不锈钢粉末的致密化行为,需在现有的烧结模型中考虑强度影响因素,才能更真实地模拟烧结过程.