A look into the cell : honey storage in honey bees, Apis mellifera

dc.contributor.authorEyer, Michael
dc.contributor.authorNeumann, Peter
dc.contributor.authorDietemann, Vincent
dc.date.accessioned2016-11-22T06:56:08Z
dc.date.available2016-11-22T06:56:08Z
dc.date.issued2016-08-25
dc.descriptionS1 Fig. Test comb appearance in colony 2. Scans were performed at A) day 1, B) day 2, C) day 5, D) day 8, E) day 12 after feeding. Cell density patterns observed on each day are depicted by icons on the right side of each picture. Note 1) the increasing density and number of filled cells; 2) the changing shape of the area of nectar containing cells due to the relocation of cell content after workers cleared cells for brood rearing (empty central area in D and E); such changes (1 and 2) also occurred in the other two colonies but with a lower frequency; 3) the dense areas of cell content neighbouring empty cells.en_ZA
dc.descriptionS2 Fig. Sugar concentration (left y-axis) and filling level (right y-axis) over time in ten individual cells per colony. Each row corresponds to a colony and shows a representative subsample of filling and ripening dynamics. The first five cells of each line represent early provisioned cells that contained solutions already at day 1 (some were relocated at a later stage); the following 5 cells represent eventually capped cells.en_ZA
dc.descriptionS1 Table. Results of Wilcoxon test comparing the filling and content concentration of early provisioned and eventually capped cells at each scan day. Significant P—values (< 0.025) after Bonferroni correction are indicated with .en_ZA
dc.descriptionS2 Table. Comparison of cell filling level and content concentration between consecutive days in early provisioned and eventually capped cells. Significant P—values (< 0.05) from the robust-ranked method (nparLD) are indicated with .en_ZA
dc.descriptionS3 Table. Results from the two-sample tests for equality of proportions between consecutive days. The test was performed for each pattern category and for the three colonies separately. Decrease or increase of proportions between the two days are indicated with < and >, respectively. Significant P—values (< 0.05) are indicated with .en_ZA
dc.descriptionS4 Table. Results of the Poisson models (log-link in glm(), R) applied for pairwise comparisons of total number of cells filled between consecutive days in each colony. Decreasing and increasing values are indicated with < and >, respectively. Significant P-values (< 0.05) are indicated with .en_ZA
dc.descriptionS5 Table. Wilcoxon-Mann-Whitney test comparing the amount of solution stored in the three colonies between consecutive days.en_ZA
dc.description.abstractHoney bees, Apis species, obtain carbohydrates from nectar and honeydew. These resources are ripened into honey in wax cells that are capped for long-term storage. These stores are used to overcome dearth periods when foraging is not possible. Despite the economic and ecological importance of honey, little is known about the processes of its production by workers. Here, we monitored the usage of storage cells and the ripening process of honey in free-flying A. mellifera colonies. We provided the colonies with solutions of different sugar concentrations to reflect the natural influx of nectar with varying quality. Since the amount of carbohydrates in a solution affects its density, we used computer tomography to measure the sugar concentration of cell content over time. The data show the occurrence of two cohorts of cells with different provisioning and ripening dynamics. The relocation of the content of many cells before final storage was part of the ripening process, because sugar concentration of the content removed was lower than that of content deposited. The results confirm the mixing of solutions of different concentrations in cells and show that honey is an inhomogeneous matrix. The last stage of ripening occurred when cell capping had already started, indicating a race against water absorption. The storage and ripening processes as well as resource use were context dependent because their dynamics changed with sugar concentration of the food. Our results support hypotheses regarding honey production proposed in earlier studies and provide new insights into the mechanisms involved.en_ZA
dc.description.departmentZoology and Entomologyen_ZA
dc.description.librarianam2016en_ZA
dc.description.sponsorshipFinancial support was granted to ME and PN by the Vinetum foundation. The Sur-La-Croix foundation is also thanked for financially supporting this study via a grant to ME.en_ZA
dc.description.urihttp://www.plosone.orgen_ZA
dc.identifier.citationEyer M, Neumann P, Dietemann V (2016) A Look into the Cell: Honey Storage in Honey Bees, Apis mellifera. PLoS ONE 11(8): e0161059. DOI: 10.1371/journal.pone.0161059.en_ZA
dc.identifier.issn1932-6203
dc.identifier.other10.1371/journal.pone.0161059
dc.identifier.urihttp://hdl.handle.net/2263/58232
dc.language.isoenen_ZA
dc.publisherPublic Library of Scienceen_ZA
dc.rights© 2016 Eyer et al. This is an open access article distributed under the terms of the Creative Commons Attribution License.en_ZA
dc.subjectCarbohydratesen_ZA
dc.subjectWorkersen_ZA
dc.subjectSugaren_ZA
dc.subjectHoneybee (Apis mellifera)en_ZA
dc.subjectStorageen_ZA
dc.titleA look into the cell : honey storage in honey bees, Apis melliferaen_ZA
dc.typeArticleen_ZA

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