Specialised woodpeckers and naturalness in hemiboreal forests – Deriving quantitative targets for conservation planning

In many parts of the world’s forests, intensive management has resulted in habitat loss for several species. Among these, specialised woodpeckers (Aves: Picidae) have been affected negatively due to their high requirements for resources that are scarce in managed forests. We used the gradient of anthropogenic impact on forests in northern Europe’s Baltic Sea region to (1) assess the relationship between the presence of four focal woodpecker species and forest naturalness and (2) quantify their requirements regarding specific resources in four different areas (south-central Sweden, southern Sweden, Lithuania and northeastern Poland). This study focused on specialised woodpecker species of the Dendropicini tribe: the three-toed (Picoides tridactylus), middle spotted (Dendrocopos medius), white-backed (Dendrocopos leucotos) and lesser spotted (Dendrocopos minor) woodpeckers. The occurrence of these species in landscape units of 100 ha was generally related positively to the degree of forest naturalness and to the amounts of resources considered critical for the suitability of their respective habitats. For the middle spotted woodpecker, basal areas 1.0 m²/ha of large-diameter deciduous trees (DBH  40 cm) were associated with a high probability of occurrence (0.9). For the white-backed woodpecker, the same probability of occurrence was found for basal areas 1.4 m²/ha of deciduous snags (DBH  10 cm). Relationships between the occurrence of the three-toed and lesser spotted woodpeckers and snag abundance were more variable among study areas. The results suggest that specialised woodpeckers would benefit from an increase in the area of forest with natural properties. Moreover, they allow defining tentative quantitative targets for sustainable forest management.     

Serological and molecular comparison of Mannheimia haemolytica and Pasteurella trehalosi strains isolated from wild and domestic ruminants in the French Alps

Over a period of 17 years, 84 bacterial isolates identified as Mannheimia haemolytica or M. glucosida, and 52 isolates identified as Pasteurella trehalosi were detected in the lungs of domestic and wild ruminants in the French Alps. The isolates were serotyped according to their surface capsular antigens, and those sharing common antigens were further characterized by pulsed field gel electrophoresis. The results showed that the bacterial isolates included in the study clustered according to the host species from which they were isolated. These findings indicate that the transmission of serotypes of M. haemolytica, M. glucosida or P. trehalosi from an animal host in which they are common to another species sharing the same geographical space may be a rare epidemiological event.     

Racemic and enantiopure synthesis and physicochemical characterization of the novel taste enhancer N-(1-carboxyethyl)-6-(hydroxymethyl)pyridinium-3-ol inner salt

Convenient syntheses were developed to obtain on a multigram scale the novel taste enhancer N-(1-carboxyethyl)-6-(hydroxymethyl)pyridinium-3-ol 1, called alapyridaine, as a racemic mixture and as pure (+)-(S) and (-)-(R) enantiomers, respectively. 5-(Hydroxymethyl)-2-furaldehyde was used as key intermediate and was reacted with l-alanine under alkaline conditions to obtain racemic 1. Alternatively, reductive amination of 5-(hydroxymethyl)-2-furaldehyde with Raney-Ni/hydrogen and l- or d-alanine followed by mild oxidation led to (+)-(S)-1 and (-)-(R)-1, respectively. Racemization was promoted under alkaline and boiling conditions via a carbanion, the formation of which was facilitated by the electron-withdrawing effect of the iminium cation and the resonance-stabilizing capacity of the pyridinium moiety. Under these conditions, 1 was obtained in a 1:1 mixture of the phenol (1) and phenolate (1-H) forms as shown by X-ray diffraction. Racemic 1 formed monoclinic crystals of high molecular organization in which the phenol-type (RS)-1, the phenolate-type (RS)-1-H, sodium cations, and ethanol molecules are present. The crystal structure of [Na(1)(1-H).(C(2)H(6)O)] shows one-dimensional mu(2)-bridging-oxygen polymers stabilized by a three-dimensional network of ionic, hydrogen bond, and pi-stacking interactions with channels occupied by solvent molecules.