Diversity and density of butterfly communities in urban green areas: an analytical approach using GIS.

BACKGROUND: Urbanization is one of the leading causes of habitat loss, habitat degradation, and fragmentation. Urban development negatively affects biodiversity. We clarified changes in butterfly communities due to urbanization in urban green areas. RESULTS: Intotal, 59 species and 1,465 individuals of butterflies were observed in the four urban green areas -Namsan Park(NS), Ewha Womans University (EW), Bukseoul Dream Forest (BD), and Hongneung Forest (HF) -anda natural forest, Gwangneung Forest (GF). The categories of land use around the study sites were determined based on GIS data. Species richness and density of niche breadth and habitat type in the four urban green areas differed mostly from those in GF. Estimated species richness and species diversity (H')in the four urban green areas were significantly lower than those in GF. Species richness and density of forest interior species and specialist species were positively correlated with paddy, field, and forest, whereas those of forest interior species and specialists were negatively correlated with urban area and road. Species composition and community structure of butterflies in the four urban were differed from those in GF. CONCLUSIONS: Theseresults suggest that decreases in paddy, field, and forest associated with the increased urban area and road negatively influenced species composition and changed butterfly communities.

Protection against TNFα-dependent liver toxicity by intraperitoneal liposome delivered DsiRNA targeting TNFα in vivo.

Tumor necrosis factor-alpha (TNFα) is a classic proinflammatory cytokine implicated in the pathogenesis of several autoimmune and inflammatory diseases including viral encephalitis. Macrophages being major producers of TNFα are thus attractive targets for in vivo RNA interference (RNAi) mediated down regulation of TNFα. The application of RNAi technology to in vivo models however presents obstacles, including rapid degradation of RNA duplexes in plasma, insufficient delivery to the target cell population and toxicity associated with intravenous administration of synthetic RNAs and carrier compounds. We exploited the phagocytic ability of macrophages for delivery of Dicer-substrate small interfering RNAs (DsiRNAs) targeting TNFα (DsiTNFα) by intraperitoneal administration of lipid-DsiRNA complexes that were efficiently taken up by peritoneal macrophages and other phagocytic cells. We report that DsiTNFα-lipid complexes delivered intraperitoneally altered the disease outcome in an acute sepsis model. Down-regulation of TNFα in peritoneal CD11b+ monocytes reduced liver damage in C57BL/6 mice and significantly delayed acute mortality in mice treated with low dose LPS plus d-galactosamine (D-GalN).

Memory characteristics of a self-assembled monolayer of Pt nanoparticles as a charge trapping layer.

A self-assembled monolayer of Pt nanoparticles (NPs) was studied as a charge trapping layer for non-volatile memory (NVM) applications. Pt NPs with a narrow size distribution (diameter ∼4 nm) were synthesized via an alcohol reduction method. The monolayer of these Pt NPs was immobilized on a SiO(2) substrate using poly(4-vinylpyridine) (P4VP) as a surface modifier. A metal-oxide-semiconductor (MOS) type memory device with Pt NPs exhibits a relatively large memory window of 5.8 V under ± 7 V for program/erase voltage. These results indicate that the self-assembled Pt NPs can be utilized for NVM devices.