In vitro evidence of root colonization suggests ecological versatility in the genus Mycena

Acknowledgements: The European commission is acknowledged for a MSCA grant to C.B.H (grant no. 658849), the University of Oslo for further funding of the project, and the Swedish University of Agricultural Sciences for hosting parts of the experiments. C.B.H was funded by an internationalisation grant from the Carlsberg Research Grant Foundation at the time of writing (grant no. CF18-0809). We would like to thank Jerome Guerrand for aid in in vitro laboratory techniques, the Norwegian Forest Seed Center for provision of seeds, Hedda Weitz and Tatiana A. Semenova-Nelson and Taina Pennanen for provision of fungal cultures. We would like to thank Marc-André Selosse, Peter Kennedy and four anonymous referees for valuable comments to an earlier version of this manuscript.Peer reviewedPublisher PD

Mycena species can be opportunist-generalist plant root invaders

ACKNOWLEDGEMENTS We thank Karl-Henrik Larsson and Arne Aronsen for provisions of specimens from the Natural History Museum of Oslo and help with the identification of field specimens from Svalbard. We further thank Cecilie Mathiesen and Mikayla Jacobs for technical assistance in the laboratory, Brendan J. Furneaux for valuable input to the R script, and the curators of H, TUR, and OULU. The Mycena ITS sequences originating from the specimens deposited in H, TUR, and OULU were produced as part of the Finnish Barcode of Life Project (FinBOL) funded by the Ministry of Environment, Finland (YM23/5512/2013), Otto A Malm's Donationsfond, and the Kone Foundation. We thank the European Commission (grant no. 658849) and the Carlsberg Foundation (grant no. CF18-0809) for grants to C.B. Harder that made this research possible. C.B. Harder was financed by a grant from the Danish Independent Research Fund DFF/FNU 2032-00064B (SapMyc) at the time of writing. Research Funding Carlsbergfondet. Grant Number: CF18-0809 Danish Independent Research Fund. Grant Number: 2032-00064B European Commission. Grant Number: 658849 Ministry of Environment, Finland. Grant Number: YM23/5512/2013Peer reviewedPublisher PD

Resveratrol inhibits benzo[a]pyrene–DNA adduct formation in human bronchial epithelial cells

Resveratrol ( trans-3,4’,5-trihydroxystilbene), a phytoalexin present in various plants and foods, has in several in vitro and in vivo studies demonstrated cancer chemopreventive and chemotherapeutic potential. We investigated the in vitro effect of resveratrol on benzo[ a] pyrene ( B[ a] P)-induced DNA adducts in human bronchial epithelial cells. This was compared to the effect of resveratrol on the expression of the cytochrome P450 (CYP) genes CYP1A1 and CYP1B1 and the formation of B[ a] P metabolites. Exposure of BEAS-2B and BEP2D cells to B[ a] P and increasing concentrations of resveratrol resulted in a dose- and time-dependent inhibition of DNA adduct formation quantified by P-32-postlabelling. Supporting this result, resveratrol was shown to inhibit CYP1A1 and CYP1B1 gene expression, as measured by real-time reverse transcriptase - polymerase chain reaction. Also, a significant correlation was found between the number of DNA adducts and the mRNA levels of these genes. Using HPLC analysis, a concomitant decrease in the formation of B[ a]P-derived metabolic products was detected. In conclusion, these data lend support to a chemopreventive role of resveratrol in polycyclic aromatic hydrocarbon-induced carcinogenesis

Ecophysiological and genetic traits of the Baltic clam Macoma balthica in the Baltic: Differences between populations in the Gdansk Bay due to acclimatization or genetic adaptation?

Normal and irregular blunt clam-shells were found. Blunt shells increased with depth, because of increasing anoxia. Minimal weight-indices and reproductive stages were found at 40 m depth (near thermo-haline stratification) probably due to spawning just before sampling. Clams from shallower stations were more ripe and heavier due to higher temperatures and re-development than at deeper stations since temperatures were still below threshold levels for spawning (10 degreesC). Respiration was at ambient temperatures acclimated to standard rates. Consequently, clams from deeper stations (with lower ambient temperatures) had 2 times higher respiration at the same test- temperature. Clams from the most shallow station (Puck Lagoon 5 m) showed the worst performance due to adverse hydrodynamics (stagnated water, anoxia). Heterozygotes showed better performance than homozygotes (heterosis). In 1995 genetic differentiation was found (Idh was diagnostic): clams below 30 m resembled Atlantic populations; shallow stations formed a distinct group (Baltic race). In later years all populations were Atlantic, probably due to inflow of North Sea water. Before 1996 ecophysiological differences between clams in the Gdansk Bay can possibly be related to genetic differentiation (adaptations of Atlantic vs. Baltic types), in later years differences were due to acclimation to ambient temperatures, salinity and oxygen levels. [KEYWORDS: genetic traits; ecophysiology; bivalve Macoma balthica stratification; adaptation Electrophoretic data; cerastoderma-edule; mytilus-edulis; temperature; systematics; energetics; bivalves; eastern; sea]