Pollen morphology of Xanthium L. (s.l.) (Asteraceae,Asteroideae, Heliantheae,Ambrosiinae) in the Iberian Peninsula - a palynotaxonomic approach to a poisonous,allergenic and invasive genus

Abstract

The pollen morphology of the Iberian taxa of the genus Xanthium s.l. and of the non-Iberian species X. ambrosioides was studied to help to identify these poisonous, allergenic and invasive taxa and clarify their taxonomic relationships. In addition, the question of the existence and structure of a mesoaperture in the apertural system of Xanthium was also considered. The pollen grains of sections Acanthoxanthium and Xanthium clearly differ by their characters, which supports the separation of both taxa and allows for their distinction based on pollen morphology. It is suggested that the morphological and palynological differences between Xanthium and Acanthoxanthium, together with the lack of hybridisation between the two sections and the monophyly of Acanthoxanthium, could lead to the elevation of the latter to the generic status. The two species of section Xanthium present in the Iberian Peninsula (X. orientale and X. strumarium) and of section Acanthoxanthium are well separated by their palynological features. Likewise, the Iberian subspecies of Xanthium, X. orientale subsp. orientale and X. orientale subsp. italicum are palynologically distinguishable. However, no significant difference could be found between the pollen of X. strumarium subsp. strumarium and of X. strumarium subsp. brasilicum. The pollen data do not support the hypotheses of a hybrid origin for X. strumarium subsp. brasilicum. A mesoaperture intersecting the foot layer and the upper part of the endexine is present in both sections, which is congruent with the results already found for other Asteroideae.     

Pharmacophores of the dual acting α, β-blockers as deduced,from molecular dynamics simulations

The dual acting α, β-blockers have an important place in the management of hypertension. Molecular dynamics simulations have been carried out on all stereoisomers of seven dual acting α, β-blockers namely adimolol, amosulalol, bucindolol, carvedilol, labetalol, medroxalol and primidolol. Three families of conformations have been identified for the group of compounds. The pharmacophores for α and β-activity have been constructed for two of these families.     

The horizontal distribution of the benthic algal flora in the Patos Lagoon estuary, Brazil, in relation to salinity, substratum and wave exposure

Monthly collections of benthic algae were made during 1 yr at 11 stations between the mouth and the salt water limits of the Patos Lagoon estuary, Brazil. A total of 94 taxa of algae were recorded, including 40 Cyanophyta, 26 Chlorophyta, 1 Xanthophyta, 3 Phaeophyta, and 24 Rhodophyta. Although the number of Rhodophyta and Phaeophyta decreased towards lower salinities, due to local salinity patterns, species substitution among the Chlorophyta and increase of Cyanophyta in the estuary, the species number remained approximately the same between the mouth and the upper saline reaches of this estuary.

The distributional limits of 64 species in the flora resulted in the formation of three algal groups of negative correlation. The horizontal distribution of each group of species was related to type of substratum, wave exposure or salinity, or a combination of these factors. The individual evaluation of the factors demonstrated that, apart from salinity, substratum and degree of exposure are of primary importance for the horizontal distribution of a large part of the algal flora in this estuary.     

Spatial and temporal patterns of distribution and abundance of a tropical fish assemblage in a seasonal Sargassum bed, Cabo Frio Island, Brazil

The patterns of distribution and abundance of a fish community were influenced by the magnitude of the canopy of Sargassum furcatum . It is suggested that the fish community in the sublittoral of Farol Beach is structured mainly by factors related to the availability of space and habitats. Quantitative data were collected by visual census techniques, along a belt of 30X2 m in each habitat. Fish diversity was greater in S. furcatum bed and in the rocks, than in the sand where there is less structural complexity. The fish density was related to the macroalgal biomass. Correspondence analysis and cluster analysis were used to describe and compare fish assemblages in three different habitats. The association observed between the juveniles of the sparid Diplodus argenteus , the grunt Haemulon aurolineatum and the surgeonfish Acanthurus bahianus and the different habitats in the summer, and juveniles of the other species in the autumn, indicates a pattern of recruitment of the species in these periods.     

Conformation of the peptide antibiotic – histatin 8 in aqueous and non aqueous media

Summary Histatin 8 (Lys¹-Phe-His-Glu-Lys⁵-His-His-Ser-His-Arg¹⁰-Gly-Tyr¹²) belongs to a group of related neutral and basic histidine rich peptides present in human salivary secretions that possess fungicidal and bactericidal activities. The conformation of this peptide has been examined by¹H and¹³C 2D-NMR in DMSO-d₆, water (pH 4.0) and 40% HFA solutions. MD simulations incorporating NMR data was used to generate the solution conformations. The structures were refined byMARDIGRAS employing theRANDMARDI approach. In both DMSO-d₆ and water, the peptide is seen to adopt a β-pleated sheet, while HFA induces an α-helix structure. The role of these structures in its mechanism of action has been explained. This article was presented at the Astra-Zeneca International Symposium on Progress in Drug Discovery and Development Sciences, Bangalore, India, 17–19 January 2001.     

Structural confirmation of spiroelliptin from Iryanthera elliptica by synthesis

Spiroelliptin, a spiro[cyclohexadienone-1,1′-tetralin] from Iryanthera elliptica, was synthesized by a novel process which involved the catalytic hydrogenation of the appropriate chalcone. This and other spiro[methoxycyclobexadienone-1,1′-tetralin] derivatives, obtained by the same process or by the oxidative coupling of the appropriate 1,3-diarylpropanes, were used as models in the compilation of ¹H and ¹³C NMR data allowing the recognition of three such naturally occurring structural types.     

(—)-Rubranine from Aniba rosaeodora

Aniba rosaeodora wood was shown to contain (—)-rubranine. An optically inactive form of this citrylidene-chalcone was previously considered to be an artifact of extraction. The constitution of rubranine was confirmed by pyrolysis and syntheses, involving previously reported pyridine-catalysed condensation of pinocembrin and citral, whereby novel intermediates were prepared, and the acid-catalysed condensation of pinocembrin with geraniol followed by oxidation.