‘Beauty bush’ and ‘twin ower’ are common names attributed to two well-recognizable species belonging to the genus Linnaea (16 spp.) – L. amabilis and L. borealis – long admired by botanists and gardeners for their perfumed paired bell-shaped owers. In the present study, we investigated their oral scent compositions through gas chro- matography – mass spectrometry (GC-MS) analysis of dynamic headspace samples. Because the owers of L. borealis in wild populations are fragrant both during the day and in the evening, circadian variation of scent emission was also assessed for this species. In total, 26 chemical compounds comprise the oral scent bouquets of L. amabilis and L. borealis, identi ed as monoterpenes (14), benzenoids and phenyl- propanoids (5), aliphatics (3), sesquiterpenes (3) and irregular terpenes (1). Whereas monoterpenes, notably (-)-α- and β-pinene, dominated the scent of L. amabilis (over 82% relative abundance), benzene derivates: 1,4 dimethoxybenzene, anisalde- hyde, 2-phenylethanol, benzaldehyde and nicotinaldehyde were exclusive to anal- ysed headspace samples of L. borealis, accounting for 52% to 100% of their relative compositions, in three Swedish populations. A southwestern Finnish population was characterized by the four rst mentioned benzenoid compounds and large amounts of (-)-α- and β-pinenes plus two aliphatic substances. e scent compounds identi- ed for both species are ubiquitous and may serve as generalist attractants/stimulants for a broad assortment of anthophilous insects. e basic work on the ower scent of L. amabilis and L. borealis should inspire studies of their pollination biology, primarily the behaviour-guiding roles of the characteristic emitted volatiles.
The genus Coreomyces (Laboulbeniaceae, Laboulbeniomycetes, Ascomycota) includes minute parasites on water boatmen (Corixidae, Hemiptera, Insecta). This taxonomic study is primarily based on freshly sampled corixids infected by Coreomyces from Sweden, although a few samples from Denmark and Turkey were also included. All records were verified using DNA sequence data from the internal transcribed spacer region and large subunit of the nuclear ribosomal DNA repeat region. We recognise four species, two of which are new to science: Coreomyces confusus H. Sundb. et al. sp. nov., C. corixae Thaxt., C. dextrorsus H. Sundb. et al. sp. nov. and C. macropus Thaxt. Coreomyces corixae is new to Denmark, Sweden and Turkey, while C. macropus is new to Denmark and Sweden. Coreomyces confusus is morphologically very similar to C. macropus and also occupies the same positions on the same host species, although it seems to be less common. Coreomyces dextrorsus resembles C. corixae morphologically but is usually considerably larger. It infects the same host species as C. corixae and also shares one of its positions on the host with C. corixae, although it is much more common in its species-specific position. All four species can inhabit two different yet distinct positions on the host. We observe that morphology is affected by the position on the host and that different species sharing the same position on the host tend to be difficult or impossible to separate on morphology only. We conclude that species circumscriptions in Coreomyces must be based on the integration of molecular and morphological data.