International honey standards are specified in a European Honey Directive and in the Codex Alimentarius Standard for Honey, both of which are presently under revision. In this article, present knowledge on the different quality criteria is reviewed. The standard drafts include standards and methods for the determination of the following quality factors: moisture, ash, acidity, HMF, apparent reducing sugars, apparent sucrose, diastase activity and water-insoluble matter. International honey standards for fructose/glucose content, the sucrose content and electrical conductivity are proposed. Also the use of other quality factors, such as invertase activity, proline and specific rotation, used in many countries, is also discussed.

No abstract

International audienc

International audienc

The identification of pollen plays an important role in ecology, palaeo-climatology, honey quality control and other areas. Currently, expert knowledge and reference collections are essential to identify pollen origin through light microscopy. Pollen identification through molecular sequencing and DNA barcoding has been proposed as an alternative approach, but the assessment of mixed pollen samples originating from multiple plant species is still a tedious and error-prone task. Next-generation sequencing has been proposed to avoid this hindrance. In this study we assessed mixed pollen probes through next-generation sequencing of amplicons from the highly variable, species-specific internal transcribed spacer 2 region of nuclear ribosomal DNA. Further, we developed a bioinformatic workflow to analyse these high-throughput data with a newly created reference database. To evaluate the feasibility, we compared results from classical identification based on light microscopy from the same samples with our sequencing results. We assessed in total 16 mixed pollen samples, 14 originated from honeybee colonies and two from solitary bee nests. The sequencing technique resulted in higher taxon richness (deeper assignments and more identified taxa) compared to light microscopy. Abundance estimations from sequencing data were significantly correlated with counted abundances through light microscopy. Simulation analyses of taxon specificity and sensitivity indicate that 96% of taxa present in the database are correctly identifiable at the genus level and 70% at the species level. Next-generation sequencing thus presents a useful and efficient workflow to identify pollen at the genus and species level without requiring specialised palynological expert knowledge.