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To link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.anbehav.2006.09.023 Byline: I.-Min Tso, Jen-Pan Huang, Chen-Pan Liao Abstract: Many studies have shown that colour signals are important in spider-insect interactions. The bright body coloration of certain orb-weaving spiders seems to serve as a visual lure to diurnal prey. However, no studies have examined whether this coloration affects spiders' nocturnal hunting. Some nocturnal lepidopteran pollinators use colour vision to locate their food resources, so orb-weaving spiders' bright coloration may also be attractive to visually oriented nocturnal insects. To assess the role of body coloration of the orchid spider, Leucauge magnifica, in luring nocturnal prey, we investigated whether: (1) these spiders actively hunt during the night; (2) nocturnal prey comprise a significant proportion of total prey intake; and (3) altering body colour signals significantly affect the nocturnal prey capture rate. Round-the-clock monitoring of L. magnifica activity patterns showed that they hunt more actively at night. Owing to the presence of relatively large moths in their diet at night, L. magnifica consumed higher prey biomass during nocturnal hunting, although this was not statistically significant owing to large variability. Painting over the spiders' yellow ventrum stripes significantly reduced their moth capture rate. These results show that certain orb-weaving spiders with bright body coloration attract nocturnal prey, and they obtain larger prey from nocturnal hunting. Author Affiliation: (a) Center for Tropical Ecology and Biodiversity, Taiwan (a ) Department of Life Science, Tunghai University, Taiwan Article History: Received 18 January 2006; Revised 10 March 2006; Accepted 13 September 2006 Article Note: (miscellaneous) MS. number: 8807R

A starlike water-soluble fullerene derivative, hexa(suffonbutyl)fullerene ([C.sub.60][([[C[H.sub.2]).sub.4]S[O.sub.3.sup.-].sub.6]; HSBF), consisting of a [C.sub.60] cage covalently bonded with six negatively charged sulfonate arms, was synthesized and used to selectively precipitate positively charged surfactants, amino acids, peptides, and proteins. The affinity of HSBF to the analytes depends on the charge, structure, and hydrophobic characteristics of the analytes. The ion pair precipitate was easily removed from the solution by centrifugation. After washing, the precipitate was redissolved in the solvent or buffer solution and the analyte was characterized by laser desorption ionization-time-of-flight mass spectrometry (LD-TOF). HSBF shows strong optical absorbance in the UV range, so no additional organic matrix was required to conduct LD-TOF analysis of small analytes. For the solution that contained five quaternary amines differing only in alkyl chain length, HSBF exhibits the highest affinity to the amine with the longest alkyl chain. Only the arginine signal was detected from the solution that contained 14 amino acids. The peptides with arginine as the end groups interacted most strongly with HSBF and could be selectively precipitated from a solution of a mixture of five peptides. The signals associated with a trace amount of charged peptides derived from the digestion of proteins by trypsin were greatly enhanced after concentration with HSBF. Among eight proteins in the sample solution, insulin had the strongest affinity to the HSBF and exhibited the strongest signal on the matrix-assisted laser desorption/ionization mass spectrum.