Bacteria Associated with a Tree-Killing Insect Reduce Concentrations of Plant Defense Compounds

Bark beetles encounter a diverse array of constitutive and rapidly induced terpenes when attempting to colonize living conifers. Concentrations of these compounds at entry sites can rapidly reach levels toxic to beetles, their brood, and fungal symbionts. Large numbers of beetles can overwhelm tree defenses via pheromone-mediated mass attacks, but the mechanisms are poorly understood. We show that bacteria associated with mountain pine beetles can metabolize monoterpenes and diterpene acids. The abilities of different symbionts to reduce concentrations of different terpenes appear complementary. Serratia reduced concentrations of all monoterpenes applied to media by 55–75 %, except for α-pinene. Beetle-associated Rahnella reduced (?)- and (+)-α-pinene by 40 % and 45 %, respectively. Serratia and Brevundimonas reduced diterpene abietic acid levels by 100 % at low concentrations. However, high concentrations exhausted this ability, suggesting that opposing rates of bacterial metabolism and plant induction of terpenes are critical. The two major fungal symbionts of mountain pine beetle, Grosmannia clavigera and Ophiostoma montium were highly susceptible to abietic acid. Grosmannia clavigera did not reduce total monoterpene concentrations in lodgepole pine turpentine. We propose the ability of bark beetles to exert landscape-scale impacts may arise partly from micro-scale processes driven by bacterial symbionts.     

Preparation of Mg–Zn bimetallic doped Na-containing bioceramic from sodium metasilicate

Glass–ceramic materials in the composition (mol%) 23.5 Na₂O–23.5CaO–xMgO–xZnO–47SiO₂–(6-2x) P₂O₅ (x = 0 and 1.5) were prepared by the sol–gel technique using sodium metasilicate (Na₂SiO₃) as source of Na₂O and SiO₂. Bioactivity was investigated in vitro by examining apatite formation on the surface of the samples after treatment in acellular simulated body fluid (SBF). Formation of bioactive apatite layer on the samples was confirmed by using scanning electron microscope, X-ray diffraction and Fourier transform infrared spectroscopy. Reactivity of the materials in SBF was based on changes in pH and ionic concentration of the solution as a function of immersion duration. Results obtained indicated that the sample doped with Mg and Zn exhibited greater crystallinity containing phases such as CaMgSi₂O₆, Ca₂MgSi₂O₇, CaSiO₃, Na₂CaSi₃O₉, Na₂CaSi₃O₈, CaZnSi₂O₇ and a new secondary phase, clinohedrite (CaZnSiO₄·H₂O), while the undoped sample contained a single crystalline phase composed of Na₂Ca₂Si₃O₉. After 7 days in SBF, phase transformation occurred at different rates on the materials leading to formation of apatite layer. The result shows that controlled amounts of MgO and ZnO may be useful in tuning up the mechanical properties of bioactive glasses while maintaining bioactivity.     

Catalytic macrocyclizations of thietanes and thiiranes by metal carbonyl complexes

This Account summarizes our recent studies of the catalytic transformations of thietanes and thiiranes by metal carbonyl complexes of the third row of the transition elements. The goal of the work has been to prepare polythioether macrocycles (thiacrowns) catalytically. This has been achieved with high success for certain thietane reactions. Thiiranes, on the other hand, tend to yield macrocyclic polydisulfides, but it has recently been found that these reactions can be redirected toward the thiacrown products by using certain alkyne carboxylates as cocatalysts. Vinylthiiranes are transformed into 3,6-dihydro-1,2-dithiins catalytically in excellent yield via W(CO)(5)(vinylthiirane) complexes.     

Disulfido metal carbonyl complexes containing manganese

An account of recent studies of the chemistry of new disulfido metal carbonyl complexes containing manganese is presented. The coordination of the disulfido ligands, the nature of reactions at the manganese atom(s) and the nature of insertion reactions at the disulfido ligands are discussed.     

A novel chelate-assisted C−C bond formation on a Cd(II) complex of an asymmetric heptadentate(N7) tripodal Schiff base ligand

Cadmium(II) complexes of some potentially heptadentate tripodal Schiff base ligands with the general formula N{(CH₂)_nNCHC₅H₄N}₂{(CH₂)_mNCHC₅H₄N}) (where n = m = 2, L₂₂₂; n = 2, m = 3, L₃₂₂; n = 3, m = 2, L₃₃₂) have been studied. These ligands are products of the full condensation of a number of tripodal tetraamines with 2-pyridinecarboxaldehyde. An unusual reaction of an additional 2-pyridine-carboxaldehyde with a methylene group adjacent to the imine bond only during template preparation of [Cd(L₃₃₂)]²⁺ was observed. The latter reaction is a novel chelate-assisted C?C bond formation because it is occurred only where a rigid five-membered chelate ring is present.     

Effect of a Rugulosin-producing Endophyte in Picea glauca on Choristoneura fumiferana

Disease-free second instar Choristoneura fumiferana (eastern spruce budworm) were placed on trees infected with a rugulosin-producing needle endophyte in two experiments. They were allowed to grow to sixth instar when survivors were collected. First, by using 3-yr old trees, a comparison was made of budworm growth on infected and uninfected trees. A second experiment used 4-yr old trees to study the effect of rugulosin content in the needle on growth. This permitted an examination of a dose response in relation to growth, and allowed us to eliminate the potential for differences in environment or foliar chemistry affecting the results. At sixth instar, budworms feeding on infected trees that contained rugulosin were smaller than those on uninfected trees. At needle concentrations above the dietary low observed effect level of rugulosin for C. fumerana >0.5 μg g⁻¹, a dose response was seen. For the first time, this demonstrates an inverse effect in outdoor nursery experiments between budworm weight and rugulosin concentration.     

机器的安全控制

机器的控制电路分为两大部分:一部分是负责机器运行功能的控制电路;另一部分是实现安全保护功能的控制电路(图1).控制电路的划分在国际标准中已有规定,而且有关"工作保护"的条目,在许多国家的法规中也可以找到.     

Environmental dust exposure as a factor contributing to an increase in Escherichia coli O157 and Salmonella populations on cattle hides in feedyards

A study was conducted to determine the impact of exposure to dust in the cattle load-out area in feedyards on pathogen contamination of cattle hides. A total of 250 cattle hides were sampled during summer and fall months, which are associated with elevated prevalence of Escherichia coli O157 in West Texas. Animals were removed from their home pens and restrained in a chute and sampled prior to exposure to dust generated as a result of a simulated loading exercise. The cattle hides were sampled again after exposure to the loading dust to determine total numbers of pathogens on cattle hides on leaving their home pen (before loading) and on cattle hides after exposure to the dust in the loading area. Air and dirt samples from the home pens and the cattle load-out area were also collected. The presence of E. coli O157 and Salmonella was determined in all the samples, and when a positive sample was identified, the total numbers of these bacteria present were enumerated. The total numbers of pathogens increased after dust exposure; Salmonella counts increased from 1.09 log most probable number (MPN)/cm2 to 1.74 log MPN/cm2 after exposure, and E. coli O157 counts increased from 0.80 to 2.35 log MPN/cm2 after sampling. E. coli O157 and Salmonella were recovered from the air samples during dust generation at 6.66 and 11.1%, respectively. Salmonella and E. coli O157 prevalence was not changed and was not associated with the exposure to the dust. Results indicate airborne dust generated as a result of cattle movement and loading could be an important determining factor in total numbers of pathogens recovered on cattle hides.     

INFLUENCE OF DAMAGE ON THE THERMAL RESPONSE OF GRAPHITE-EPOXY LAMINATES

A “constrained ” displacement finite element approach for studying the influence of transverse cracks and delaminations on the thermal response of laminated composites is presented. Typical results are given in the form of percent retention curves for the coefficient of thermal expansion as a function of crack density. Cross-ply and quasi-isotropic T300/5208 graphite-epoxy laminates are considered. It is shown that transverse cracks can have a significant influence on the coefficient of thermal expansion, but delaminations located symmetrically about the laminate mid-plane have no influence on thermal expansion.