Centipede specimens, litter and soil material were dried at 60°C for 24 h. For measuring stable isotope ratios whole centipede specimens were used whenever possible; large animals exceeding the limits of the analysis system were homogenized with a mortar and pestle and an aliquot was used for measuring stable isotope values. Replicates from different sites were analyzed for each species whenever possible. Before measurement litter and soil material was dried and ground with a ball mill (Retsch Mixer Mill MM200, Haan, Germany). Stable isotope ratios, carbon and nitrogen concentrations of animals and of litter and soil material were determined using a coupled system of an elemental analyzer (NA 1500, Carlo Erba, Milan, Italy) and a mass spectrometer (MAT 251, Finnigan, Bremen, Germany) [38 ]. Isotopic values were expressed using the δ notation with δX (‰) = (Rsample−Rstandard) / Rstandard x 1000, with X representing the target isotope (15N or 13C) and R the ratio of the heavy to the light isotope (13C/12C and 15N/14N, respectively). Nitrogen in atmospheric air and Vienna PD Belemnite served as standard for 15N and 13C, respectively, and acetanilide for internal calibration. Stable isotope values of animals are given as difference to the values of leaf litter sampled from the study sites, i.e. by calculating Δ13C and Δ15N values [39 ].
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