Post-mortem volatiles of vertebrate tissue

Volatile emission during vertebrate decay is a complex process that is understood incompletely. It depends on many factors. The main factor is the metabolism of the microbial species present inside and on the vertebrate. In this review, we combine the results from studies on volatile organic compounds (VOCs) detected during this decay process and those on the biochemical formation of VOCs in order to improve our understanding of the decay process. Micro-organisms are the main producers of VOCs, which are by- or end-products of microbial metabolism. Many microbes are already present inside and on a vertebrate, and these can initiate microbial decay. In addition, micro-organisms from the environment colonize the cadaver. The composition of microbial communities is complex, and communities of different species interact with each other in succession. In comparison to the complexity of the decay process, the resulting volatile pattern does show some consistency. Therefore, the possibility of an existence of a time-dependent core volatile pattern, which could be used for applications in areas such as forensics or food science, is discussed. Possible microbial interactions that might alter the process of decay are highlighted

Mammal pollinators lured by the scent of a parasitic plant

To communicate with animals, plants use signals that are distinct from their surroundings. Animals generally learn to use these signals through associative conditioning; however, signals are most effective when they elicit innate behavioural responses. Many plant species have flowers specialized for pollination by ground-dwelling mammals, but the signals used to attract these pollinators have not been elucidated. Here, we demonstrate the chemical basis for attraction of mammal pollinators to flowers of the dioecious parasitic plant Cytinus visseri (Cytinaceae). Two aliphatic ketones dominate the scent of this species; 3-hexanone, which elicits strong innate attraction in rodents, and 1-hexen-3-one, which repels them in isolation, but not in combination with 3-hexanone. The aliphatic ketone-dominated scent of C. visseri contrasts with those of insect-pollinated plants, which are typically dominated by terpenoids, aromatic or non-ketone aliphatic compounds. 3-hexanone is also known from some bat-pollinated species, suggesting independent evolution of plant signals in derived, highly specialized mammal-pollination systems. © 2011 The Royal Society

Pollination ecology of Magnolia ovata may explain the overall large flower size of the genus

Flowering and fruiting biology of Magnolia ovata was studied in Atlantic forests in the interior of São Paulo State, Brazil. The large, bisexual flowers are protogynous, nocturnal, thermogenic and emit a strong scent in two consecutive evenings. In the first night of anthesis, the flowers are in the pistillate stage and thermogenesis starts at about sunset and lasts about 3. h. In the second night, the flowers enter the staminate stage and produce heat for 4. h. Heat is generated by the petals, gynoecium and anthers. Temperatures measured inside the petals reach 26.7°C and 31.9°C in the pistillate and staminate stages, 6.0 and 10.6°C above ambient air, respectively. In the pistillate stage, the perianth opens after sunset and closes tightly a few hours later, and remains closed until the next evening. The initial opening and closing, however, is not synchronous for all flowers during the night. In the following evening, flowers in the staminate stage again open and remain so until the petals drop. Scent compounds, analyzed by GC-MS, contain C5-branched chain compounds, aliphatics, benzenoids and monoterpenoids. Emission of the most prominent compound, C5-branched methyl 2-methyl butyrate, commences before flower opening and continues throughout anthesis, but is accentuated in the thermogenic pistillate and staminate stages. Female and male individuals of only one beetle species, the dynastid scarab Cyclocephala literata, are attracted to the scented flowers in both pistillate and staminate stages. Once inside the flowers they feed on the petals and mate. Tests with synthetic methyl 2-methyl butyrate indicate that this compound is a strong attractant for the beetles. Because this scent compound is strongly emitted in both pistillate and staminate stages, the beetles fly indiscriminately between flowers of both stages. This behavior enhances pollen mixing and effective cross-pollination of the self-compatible species. The evolutionary history of Magnolia appears to be influenced by an ancestral condition of dynastid scarab beetle pollination. Large magnolia flowers are best explained as an archaic structure resulting from the initial association of tropical American species of section Talauma with large and voracious dynastid beetles. © 2011 Elsevier GmbH.Gerhard Gottsberger, Ilse Silberbauer-Gottsberger, Roger S. Seymour and Stefan Dötter

Nursery pollination by a moth in Silene latifolia: the role of odours in eliciting antennal and behavioural responses

Since the 1970s it has been known that the nursery pollinator Hadena bicruris is attracted to the flowers of its most important host plant, Silene latifolia, by their scent. Here we identified important compounds for attraction of this noctuid moth. Gas chromatographic and electroantennographic methods were used to detect compounds eliciting signals in the antennae of the moth. Electrophysiologically active compounds were tested in wind-tunnel bioassays to foraging naive moths, and the attractivity of these compounds was compared with that to the natural scent of whole S. latifolia flowers. The antennae of moths detected substances of several classes. Phenylacetaldehyde elicited the strongest signals in the antennae, but lilac aldehydes were the most attractive compounds in wind-tunnel bioassays and attracted 90% of the moths tested, as did the scent of single flowers. Our results show that the most common and abundant floral scent compounds in S. latifolia, lilac aldehydes, attracted most of the moths tested, indicating a specific adaptation of H. bicruris to its host plant

Linalool and lilac aldehyde/alcohol in flower scents - Electrophysiological detection of lilac aldehyde stereoisomers by a moth

The stereoisomers of linalool and lilac aldehyde/alcohol were determined in the flower scent of 15 plant species using enantioselective multidimensional gas chromatography/mass spectrometry (enantio-MDGC/MS). Both linalool and all 8 stereoisomers of lilac alcohol and lilac aldehyde were detected, and there was a species-specific pattern. Single stereoisomers were collected by micropreparative-enantio-MDGC and were electrophysiologically tested on antennae of the noctuid moth Hadena bicruris, a species known to rely on lilac aldehyde for finding its host plant. The moth responded to all 8 stereoisomers, though only four stereoisomers were found in the scent of its host plant. The moth was less sensitive to some isomers than to others. (c) 2006 Elsevier B.V. All rights reserved

Floral scent of brazilian Passiflora: five species analised by dynamic headspace

ABSTRACT This study describes for the first time the chemical composition and olfactive description of floral scent from Brazilian Passiflora (Passiflora edulis Sim, Passiflora alata Curtis, Passiflora cincinnata Mast., Passiflora coccinea Aubl. and Passiflora quadrangularis L.). Five species were grown in greenhouse at the Agronomic Institute (IAC), São Paulo, Brazil. Volatile compounds were collected using dynamic headspace. Analyses of scent composition were performed by gas chromatograph coupled to mass spectrometer. Identification of chemical constituents was conducted through of retention index followed by comparative analysis of mass spectra with specialized databases. The olfactive descriptions of floral scent from each species was evaluated for a professional perfumer. High interspecific diversity was found between chemical compositions of floral scent within Passiflora and different bouquets were observed amount the studied species. Mayor constituents were linalool (P. alata), geraniol (P. quadrangularis), 1,4-dimethoxybenzene (P. edulis), benzaldehyde (P. cincinnata) and 2-methyl-3-pentanone (P. coccinea)