Data from: Diverse pollen nutrition can improve the development of solitary bees but does not mitigate negative pesticide impacts
Data files
Jan 21, 2024 version files 381.99 KB
-
Development_data.csv
368.56 KB
-
Gene_expression_data.csv
9.20 KB
-
README.md
4.22 KB
Abstract
Floral resource loss and pesticide exposure are major threats to bees in intensively managed agroecosystems, but interactions among these drivers remain poorly understood. Altered composition and lowered diversity of pollen nutrition may reinforce negative pesticide impacts on bees. Here we investigated the development and survival of the solitary bee Osmia bicornis provisioned with three different pollen types, as well as a mixture of these types representing a higher pollen diversity. We exposed bees of each nutritional treatment to five pesticides at different concentrations in the laboratory. Two field-realistic concentrations of three nicotinic acetylcholine receptor (nAChR) modulating insecticides (thiacloprid, sulfoxaflor and flupyradifurone), as well as of two fungicides (azoxystrobin and tebuconazole) were examined. We further measured the expression of two detoxification genes (CYP9BU1, CYP9BU2) under exposure to thiacloprid across different nutrition treatments as a potential mechanistic pathway driving pesticide-nutrition interactions. We found that more diverse pollen nutrition reduced development time, enhanced pollen efficacy (cocoon weight divided by consumed pollen weight) and pollen consumption, and increased weight of O. bicornis after larval development (cocoon weight). Contrary to fungicides, high field-realistic concentrations of all three insecticides negatively affected O. bicornis by extending development times. Moreover, sulfoxaflor and flupyradifurone also reduced pollen efficacy and cocoon weight, and sulfoxaflor reduced pollen consumption and increased mortality. The expression of detoxification genes differed across pollen nutrition types, but was not enhanced after exposure to thiacloprid. Our findings highlight that lowered diversity of pollen nutrition and high field-realistic exposure to nAChR modulating insecticides negatively affected the development of O. bicornis, but we found no mitigation of negative pesticide impacts through increased pollen diversity. These results have important implications for risk assessment for bee pollinators, indicating that negative effects of nAChR modulating insecticides to developing solitary bees are currently underestimated.
https://doi.org/10.5061/dryad.73n5tb33d
DATA & FILE OVERVIEW
File List & Short Description:
-
Development_data.csv:
Data collected for individual developing bees -
Gene_expression_data.csv
Data collected for analysis of gene expression levels of detoxification genes (CYP9BU1 and CYP9BU2)
DATA-SPECIFIC INFORMATION
Variable List
SPECIFIC DATASET - Development_data.csv
- plate: number of wooden plate on which the developing bee was located
- position: position (A-I) on the wooden plate on which the developing bee was located
- pesticide: pesticide to which the bee was exposed (or not exposed, if it was a control bee, see concentration.factor)
- concentration.factor: pesticide concentration to which the bee was exposed
(low: low concentration, high: high concentration, c: water-only-control, ac: water-acetone-control) - concentration.ppb: concentration of the pesticide used (in ppb, µg/kg)
- nutrition: pollen nutrition type offered to the developing bee (as pollen provision)
- egg.collection: date of egg collection (start of exposure to pesticide/control)
- larva: date on which the developing bee reached the larval stage
- feeding.larva: date on which the developing bee started feeding on the pollen provision
- feeding.defecating.larva: date on which the bee larva started to defecate
- spinning.larva: date on which the bee larva initiated cocoon spinning (used to calculate development time)
- pale.cocoon: date on which the bee larva finished cocoon spinning, cocoon still pale
- dark.cocoon: date on which the finished cocoon appeared dark
- death.larva: date on which the bee larva was observed dead (in case it died)
- incubation.emergence: date on which the cocoon was incubated at room temperature after wintering in order for the adult bee to emerge
- date.emergence: date on which adult bee emerged from cocoon (and was released outdoors)
- emergence.status: indicates whether bee emerged from cocoon as adult or not
- sex: sex of bee (either determined after emergence or - in case bee did not emerge - after opening the cocoon)
- development.time.days: number of days needed from hatching from the egg until cocoon spinning
- pollen.consumed.mg: amount of pollen consumed by bee larva (400 mg were provided)
- pollen.fully.consumed: binary variable indicating whether the total amount of pollen (400 mg) was consumed (1) or not (0)
- pollen.efficacy: cocoon weight/pollen consumed (mg/mg)
- cocoon.weight.mg: weight of cocoon before wintering (after completed metamorphosis, mg)
- survival: indicates whether a bee survived and successfully emerged as adult or not
- comment: any additional comments for a sample
- NOTE on cells containing NA: In case a developing bee died, NAs were inserted in the data table for the developmental stages that were not observed for this individual and for the measurements that could not be taken. For surviving bees, “death.larva” was set to NA. Additionally, in several cases, specific developmental stages could not be observed for some developing bees, e.g., in case a larva was already in the “feeding.larva” stage when it was first observed as larva.
SPECIFIC DATASET - Gene_expression_data.csv
- sample.id: ID of developing bee (sample)
- pesticide: pesticide to which the bee was exposed (or not exposed, if it was a control bee, see concentration.factor)
NOTE: only thiacloprid was used in the gene expression experiment - concentration.factor: pesticide concentration, to which the bee was exposed
(high: high concentration (0.75 mg/kg thiacloprid), ac: water-acetone-control) - nutrition: pollen nutrition type offered to the developing bee (as pollen provision)
- gene: gene of which expression level was measured (CYP9BU1 or CYP9BU2)
- fold.change: gene expression level measured as 2^-ΔΔct, reference level is mix nutrition water-acetone-control