Evaluation of traps of six different designs to capture pine sawyer beetles (Coleoptera: Cerambycidae)

1 Sawyer beetles (Coleoptera: Cerambycidae) and metallic wood‐boring beetles (Coleoptera: Buprestidae) attack recently killed or felled trees. They are attracted to potential hosts by volatiles and possibly by visual cues. We examined traps of six different designs to determine the role of silhouette and shape in the capture of pine sawyer beetles, Monochamus L. 2 Traps with a round black cylinder, a single vane (clear or black), or cross vanes (clear or black) all mounted above a pan were compared to an open pan. Each pan contained soapy water to retain insects. 3 Traps with a black silhouette were significantly more effective in capturing male and female Monochamus scutellatus (Say) than traps with or without clear vanes. For both sexes of M. mutator LeConte, pan traps were as effective as traps with a black silhouette. Silhouette was not important for the capture of male and female M. notatus (Drury). Trap catches for the six trap types were not significantly different for male Buprestis maculativentris Say. 4 A pan trap with a black silhouette is recommended for general use in capturing wood‐boring cerambycids and buprestids.     

Effects of polycyclic aromatic hydrocarbons on molluscan lysosomes and endoplasmic reticulum

Summary Some effects of two isomeric polycyclic aromatic hydrocarbons, anthracene and phenanthrene, on the fine structure and cytochemistry of digestive cells in the marine musselMytilus edulis have been investigated. The cytochemical results show that increasing concentrations of anthracene and phenanthrene have different effects on the acid labilization time for laten -glucuronidase which is used to measure the stability of lysosomal membranes. At the ultrastructural level the limiting membranes of secondary lysosomes appear multilayered, with discontinuities and overlaps. Under the conditions of the experiment, only phenanthrene produces changes in this configuration. Both macroautophagic and microautophagic processes occur in the control and hydrocarbon treatments, and complementary data from other studies indicate that autophagic processes are enhanced by polycyclic aromatic hydrocarbons. Phenanthrene also causes proliferation of the smooth endoplasmic reticulum in the digestive cells, although cytochemical measurements of smooth endoplasmic reticulum-associated NADPH-ferrihemoprotein reductase show that anthracene stimulates activity over a greater range of concentrations than phenanthrene. The different effects of the two isomers is taken as evidence that the molecular configuration of the compound determines its reactivity with membranes and its subsequent effect on the physiology of the cells.     

Structural and functional analysis of phosphothreonine-dependent FHA domain interactions

FHA domains are well established as phospho-dependent binding modules mediating signal transduction in Ser/Thr kinase signaling networks in both eukaryotic and prokaryotic species. Although they are unique in binding exclusively to phosphothreonine, the basis for this discrimination over phosphoserine has remained elusive. Here, we attempt to dissect overall binding specificity at the molecular level. We first determined the optimal peptide sequence for Rv0020c FHA domain binding by oriented peptide library screening. This served as a basis for systematic mutagenic and binding analyses, allowing us to derive relative thermodynamic contributions of conserved protein and peptide residues to binding and specificity. Structures of phosphopeptide-bound and uncomplexed Rv0020c FHA domain then directed molecular dynamics simulations which show how the extraordinary discrimination in favor of phosphothreonine occurs through formation of additional hydrogen-bonding networks that are ultimately stabilized by van der Waals interactions of the phosphothreonine γ-methyl group with a conserved pocket on the FHA domain surface.     

Dynamic rearrangement of the filamentous actin network occurs during zoosporogenesis and encystment in the oomycete phytophthora cinnamomi

The organization of filamentous actin (F-actin) in living cells of the oomycete Phytophthora cinnamomi was determined during zoosporogenesis and zoospore encystment by microinjecting sporangia with fluorescently labeled phalloidin and observing resultant fluorescence by confocal microscopy. In multinucleate sporangia prior to the induction of cleavage, phalloidin labeling took the form of plaques which occurred mainly in the periphery of the sporangia. After induction of cleavage, phalloidin labeling showed that the plaques disappeared and that F-actin began to accumulate along the developing cleavage planes and around nuclei and water expulsion vacuoles. F-actin labeling was also observed near the plasma membrane in zoospores and young cysts but reverted to the plaque form in older cysts. Localization of F-actin close to the developing cleavage planes is consistent with the idea that actin microfilaments function in the positioning and expansion of the cleavage membranes. Observations of plaques of actin in living sporangia provide evidence that plaques are not aldehyde-induced fixation artifacts. Copyright 1998 Academic Press.     

Serglycin expression during monocytic differentiation of U937-1 cells

Serglycin is the major proteoglycan in most hematopoietic cells, including monocytes and macrophages. The monoblastic cell line U937-1 was used to study the expression of serglycin during proliferation and differentiation. In unstimulated proliferating U937-1 cells serglycin mRNA is nonconstitutively expressed. The level of serglycin mRNA was found to correlate with the synthesis of chondroitin sulfate proteoglycan (CSPG). The U937-1 cells were induced to differentiate into different types of macrophage-like cells by exposing the cells to PMA, RA, or VitD3. These inducers of differentiation affected the expression of serglycin mRNA in three different ways. The initial upregulation seen in the normally proliferating cells was not observed in PMA treated cells. In contrast, RA increased the initial upregulation, giving a reproducible six times increase in serglycin mRNA level from 4 to 24 h of incubation, compared to a four times increase in the control cells. VitD3 had no effect on the expression of serglycin mRNA. The incorporation of (35S)sulfate into CSPG decreased approximately 50% in all three differentiated cell types. Further, the (35S)CSPGs expressed were of larger size in PMA treated cells than controls, but smaller after RA treatment. This was due to the expression of CSPGs, with CS-chains of 25 and 5 kDa in PMA and RA treated cells, respectively, compared to 11 kDa in the controls. VitD3 had no significant effect on the size of CSPG produced. PMA treated cells secreted 75% of the (35S)PGs expressed, but the major portion was retained in cells treated with VitD3 or RA. The differences seen in serglycin mRNA levels, the macromolecular properties of serglycin and in the PG secretion patterns, suggest that serglycin may have different functions in different types of macrophages.      

C(4) Pathway Photosynthesis at Low Temperature in Cold-tolerant Atriplex Species

Two species of Atriplex were grown under low temperature (8 C day/6 C night) and high temperature (28 C day/20 C night) regimes. The photosynthetic capacity of these plants was studied as a function of temperature in a leaf gas exchange cuvette. Both species showed substantial photosynthetic capacity between 4 and 10 C and this was not enhanced by growth at low temperatures but rather, was somewhat greater in plants grown at higher temperature. Photosynthetic capacity of low temperature-grown plants at high temperature was greater in Atriplex confertifolia (Torr. and Frem.) S. Watts., a native of cool deserts, than in Atriplex vesicaria (Hew. ex. Benth.) from warmer desert areas. Leaves of both species were also subjected to ¹⁴CO₂ pulse-chase and steady-state feeding experiments under controlled temperature conditions. These experiments revealed that the kinetics of carbon assimilation through the intermediates of the C₄ pathway is not substantially disrupted at low temperature in either species. There was, however, a substantial interchange of label between aspartate and malate at low temperature which was not evident at high temperature. There was also an increase in the pool sizes of the C₄ acids involved in photosynthesis of A. confertifolia. Speculation as to the explanation of these changes and their possible significance in promoting low temperature C₄ photosynthesis in these plants is presented.