The mechanistic origin of amber pigmentation of Perithemis tenera (Say, 1840) wings (Odonata: Libellulidae) and its function in conspecific signalling.

Animal coloration serves various signaling and non-signaling functions. In damselflies and dragonflies (Odonata), such colors may not only play photoprotective and/or thermoregulatory roles but also serve as visual signals during courtship and/or agonistic interactions. Here, we analyzed the coloration of Perithemis tenera wings, a potential secondary sexual ornament, applying spectrophotometry and visual modeling to gain a deeper understanding of their color mechanisms and functions.

A meta-analysis on alternative mating tactics: when the main and the alternative yield similar reproductive success.

In many species, individuals of the same sex exhibit different mating behaviours, a phenomenon known as alternative mating tactics (AMTs). These AMTs may occur in species in which morphology prevents individuals from adopting different tactics (fixed expression of AMTs) as well as in species in which individuals can alternate between them (flexible expression of AMTs). Regardless of the way different mating tactics are expressed, a key point to understanding the selective forces driving AMT evolution relies on identifying differences in the reproductive success between tactics.

NMR spectral assignments of a new [C--O--C] isoflavone dimer from Andira surinamensis.

The phytochemical investigation of extracts from the branch wood and branch barks of Andira surinamensis yielded a novel isoflavone dimer, 4'-methoxyisoflavone-(7-O-7'')-3''',4'''-methylenedioxyisoflavone (surinamensin), along with the triterpene lupeol and the known isoflavones 5,7-dihydroxy-4'-methoxyisoflavone (biochanin A), 5,4'-dihydroxy-7-methoxyisoflavone (prunetin), 7,3'-dihydroxy-4'-methoxyisoflavone (calycosin), and 5,7,3'-trihydroxy-4'-methoxyisoflavone (pratensein). The structure of the new isoflavone was elucidated by 1D and 2D homonuclear and heteronuclear NMR spectroscopy and by comparison with published data for closely related compounds.