The health of honey bee colonies is, amongst others, affected by the amount, quality and diversity of available melliferous plants. Since landscape is highly diverse throughout Austria regarding the availability of nutritional resources, we used data from annual surveys on honey bee colony losses ranging over six years to analyse a possible relationship with land use. The data set comprises reports from a total of 6,655 beekeepers and 129,428 wintered honey bee colonies. Regions surrounding the beekeeping operations were assigned to one of six clusters according to their composition of land use categories by use of a hierarchical cluster analysis, allowing a rough distinction between urban regions, regions predominated by semi-natural areas and pastures, and mainly agricultural environments. We ran a Generalised Linear Mixed Model and found winter colony mortality significantly affected by operation size, year, and cluster membership, but also by the interaction of year and cluster membership. Honey bee colonies in regions composed predominantly of semi-natural areas, coniferous forests and pastures had the lowest loss probability in four out of six years, and loss probabilities within these regions were significantly lower in five out of six years compared to those within regions composed predominantly of artificial surfaces, broad-leaved and coniferous forest.
Honey bees (Apis mellifera) play an essential role in the ecosystem by pollinating wild and cultivated plants. In recent years, high mortality of honey bee colonies has been reported from many regions of the world1,2,3,4,5. The drivers of such losses include several biotic and abiotic factors, and synergistic actions of multiple actors are likewise believed to affect colony health6,7,8,9.
For wild bees, which greatly depend on their nesting habitats, landscape composition strongly influences their total abundance and species richness, reflected for instance in Simpson’s diversity10,11. The nature of the resource providing unit, which is defined as “environmental components around the hive including contaminants”12, also affects managed honey bee colonies. Some types of landscape may be better suited for honey bees than others13. Against this backdrop, the effect of the honey bees’ exposure to forage plants with agriculturally administered insecticides is of particular interest. The use of neonicotinoid insecticides threatens bees; research on this topic has, however, been surrounded by controversy14,15. Ingestion of sublethal doses results in deficiencies in the bees’ performance, which was demonstrated for various parameters including colony development and survival16,17,18. There are only few field studies that focused directly on the effects of insecticide-treated crops on honey bees with at least partially contradictory results17,19,20,21,22,23,24,25,26.
Alburaki et al. conducted two studies27,28 in Quebec, Canada in order to analyse the impact of neonicotinoid pesticides on honey bee health by placing honey bee colonies in different agricultural environments (neonicotinoid-treated and untreated cornfields). The results indicate a higher load of Varroa destructor mites and a higher prevalence of black queen cell virus (BQCV) for colonies placed in treated areas, whereas no clear effect was found on weight and brood. Two other studies from Alburaki et al.29,30 performed in Tennessee, USA also aimed at investigating the effect of landscape and pesticides on honey bee health. While foragers’ mortality did not differ between agricultural and non-agricultural landscapes30, differences became apparent in biological traits of honey bee colonies according to the intensity of agricultural use29. It should, however, be noted that the number of observed colonies was relatively small (four to thirty-two) and that the maximum period of observation was two years.
Besides exposure to insecticides, land cover influences the wellbeing of honey bee colonies also via the amount, quality and seasonal pattern of nutritional resources provided31. Diversity and quality of collected pollen forage affects honey bee health and varies depending on season and landscape composition32,33,34. Danish hive scale data also suggests that colonies gain more honey in landscapes composed of more than 50% urban areas compared to other landscapes35.
In many countries, standardised large scale data collection on honey bee colony losses was put into practice only recently36,37,38. The data are based on self-reports by beekeepers and allow epidemiologic analyses of operational drivers such as hive management techniques. Colony loss data can for instance be used to identify best practice of hive management and treatment of colonies against the parasitic mite Varroa destructor2,3,39. Combinations of such survey based data with other available data sets or further sample analysis have been shown to facilitate our understanding of honey bee health17,40.
In Austria, data on winter mortality of honey bee colonies are available from the winter 2007/08 onwards, with increasing sample size and spatial accuracy over the years36,41. The number of responses increased over the years and now covers approximately five percent of all registered Austrian beekeepers from each region of the country38. A previous study used parts of this data set to investigate how long-term weather conditions influence honey bee colony winter mortality rates. Statistical correlations between monthly climate variables and winter mortality rates demonstrated that warmer and drier weather conditions in the year preceding the winter are generally accompanied by increased loss rates of honey bee colonies during the respective winter42.
The only study so far that connected larger data sets of honey bee colony winter losses and land use analysed data from 166 to 188 apiaries for three consecutive winters in Luxembourg13. They found 60 out of 133 land cover classes to be correlated with bee colony losses, with the majority of these classes being associated with human activities other than agriculture. The study further suggests that significant effects may be found in some years or certain parts of the country only. In the present study, we investigate the impact of land cover on colony winter mortality in Austria with a much larger dataset for six consecutive years, including two winters with high losses and one winter with a very low loss rate.
Material and Methods
The study at hand is based on data from the Austrian monitoring scheme of honey bee winter losses. Within the scope of the COLOSS questionnaire used to collect data, apiarists are annually encouraged to report their winter losses voluntarily and optionally anonymously37,41. The gathered information comprises specifications on the location of the beekeeping operation, the total number of wintered colonies and the number of lost colonies (i.e. the sum of dead colonies and colonies with queen problems) for the winters from 2010/11 to 2015/16. The locations of the beekeeping operations were recorded on the level of municipality in order to ensure beekeeper anonymity, i.e. exact coordinates were not available for the analysis. In Austria, municipalities are very heterogeneous in size. The area of the 2,354 municipalities ranges from 11 to 46,680 ha with an average size of 3,563 ha. To facilitate comparability, municipalities were aggregated into more homogeneous regions, resulting in 263 regions with an average size of 31,890 ha. These regions are based on the locations of the meteorological stations, listed in the yearbook of Austria’s Central Institute for Meteorology and Geodynamics (ZAMG43), which are evenly distributed across Austria. For the determination of the regions, each municipality was assigned to the nearest meteorological station (based on the distance between municipality centroid and meteorological station) and municipalities assigned to the same station were combined into one region. For each region, the elevation above sea level was determined at its centroid in order to analyse the possible relation between altitude and winter losses.
The questions in the COLOSS questionnaire were slightly adapted over the years. As of 2011, beekeepers were also asked to specify whether they kept migratory colonies, but no further details on the time of migration or the other locations were available. In a pre-analysis, we modelled the winter losses for each year separately and tested the significance of the migratory effect. As the migratory effect was not significant in the majority of the models, we treat all apiaries as if they were stationary. Due to the vague information that is available on migration, no indication is given that our assumption may cause systematic bias in the reported analysis.
Information on land cover in Austria comprises data from three different data sources: INVEKOS (Integrated management and monitoring system from the Austrian Federal Ministry of Agriculture, Forestry, Environment and Water Management44), BFW (Woodland map of the Austrian Research Centre for Forests45) and CORINE (Coordination of Information on the Environment CORINE Landcover46). INVEKOS provides the most detailed information on agricultural land use in Austria. Approximately 300 land cover categories (e.g. pastures, crop, oil fruits) which are assigned to seven main categories are surveyed and available on a yearly basis. We predominantly used the main categories as defined by INVEKOS. Only land cover subcategories discussed as possibly influencing honey bee health, such as maize19,26,27,28, oil fruits/oilseed25, potatoes and protein plants, were kept as separate subcategories. Cereal crops other than maize are contained in a separate category ‘crop excl. maize’. Field crops that do not fall into the categories cereal crops, oil fruits/oilseed, potatoes and protein plants are summarised in a broader category ‘other field crops’. The BFW data set is based on satellite images from the years 2000–2003 and includes the categories ‘coniferous forest’, ‘broad-leaved forest’, ‘mixed forest (mainly coniferous)’, ‘mixed forest (mainly broad-leaved)’ and ‘clearcutting’. The European land cover programme CORINE provides 47 land cover categories on cropland, artificial surfaces, urban facilities (including parks/sports facilities) and wetlands. CORINE data is updated every six years. At the time of the analysis, the most recent data set was based on the reference year 2012. As some categories overlap between the different data sources, we considered cropland categories only from the INVEKOS data, woodlands only from the BFW, and wetlands only from the CORINE data, as these seemed the most reliable sources for the respective categories. Examination of the available land cover categories resulted in 247 relevant categories, which were thematically summarised into 22 main categories. These 22 land cover categories comprise 13 agricultural land use categories from the INVEKOS data set, 5 woodland categories from the Austrian Research Centre for Forests (BFW), and 4 further categories from the CORINE data set: wetlands/water bodies, artificial surfaces, urban parks/sport facilities, and semi-natural areas. Semi-natural areas include the sub-categories ‘Scrub and/or herbaceous vegetation associations’, ‘Open spaces with little or no vegetation’ and the unclassified land/water areas. Figure 1 lists the considered land use categories and shows the total area covered by each category in 2014. This figure shows that Austria is to a large extent covered by coniferous forests, followed by grassland and semi-natural habitats.
The relation of land use and honey bee winter losses was modelled using a Generalised Linear Mixed Model (GLMM). The unit of observation was one colony within a beekeeping operation. Hence, information on winter losses could be considered as a binary response (success/failure of overwintering). Consequently, the binomial distribution and the logit-link function were assumed for the model. As the land use categories are highly correlated, see Supplementary Figures S1–S2, they were not directly used as explanatory variables in the model. Instead, a hierarchical cluster analysis was conducted to group regions that show similarities regarding their land cover composition. Similarity was defined by means of correlation-based distance matrices47. Two regions are considered as being related if land use in these regions is highly correlated. For the land use categories associated with cropland, data was available on a yearly basis. Therefore each year-region combination was considered for the cluster analysis. The clustering was performed hierarchically, i.e., initially, each region forms its own cluster. Successively, the two most related clusters are combined in each step until only one cluster remains47. This process can then be visualised in the form of a dendrogram, which was used to select a complete partitioning of six clusters for further analysis. Each beekeeping operation was then allocated to one of the six clusters according to the land cover composition in its respective region. For each cluster, the proportion of lost colonies and corresponding 95% exact Clopper-Pearson confidence intervals48 were determined in a first descriptive analysis. In the subsequent multivariate model, the cluster membership of each operation was considered as a possible risk factor for winter losses.
Although land use was the main variable of interest, winter losses may further be influenced by a complex combination of different risk factors. In order to consider other sources of risk, the total number of wintered colonies, the municipality size and the elevation above sea level of the region in which the apiaries are located were considered as confounder variables. The size of the municipality was evenly categorised into four classes according to the corresponding quartiles and considered as a factor in the model. The classes are as follows:
very small, if the overall area of municipality ≤1,620 ha
small, if the overall area of municipality ∈(1,620 ha; 2,800 ha]
medium, if the overall area of municipality ∈(2,800 ha; 4,700 ha]
large, if the overall area of municipality >4,700 ha.
Switanek et al.42 showed the climate to be among the relevant factors for honey bee winter mortality. In particular, the study results indicate that the weather conditions in the preceding year have a significant influence on winter mortality, and warmer and drier weather was associated with higher losses. In our model, however, information on weather conditions was not available for the whole study period and, hence, not incorporated in the model. As weather conditions were not the main interest factor of the study at hand, the year of observation was considered as an additional risk factor to account for different unobserved environmental conditions. In order to deal with possible overdispersion in the data, an ID was assigned to each data set within a year and this ID was considered as a random effect in the model.
Model selection was performed through forward selection; the Akaike Information Criterion (AIC) and likelihood-ratio tests served as model selection criteria. Significant factors were identified at the significance level α = 0.05. The model selection process is further described in Supplementary Table S1. All statistical analyses were performed in R, version 3.3.249 using the R packages binGroup48, lme450 and ggplot251.
Results and Discussion
Honey bee winter losses
The available data from questionnaires on honey bee winter mortality comprises reports from a total of 6,670 beekeepers. Observations from 15 beekeepers were excluded due to missing information on beekeeping operation location. The remaining beekeepers in total wintered 129,428 colonies between the winters of 2010/11 and 2015/16. The lowest number of reporting beekeepers was 559 in the winter of 2010/11; the winter of 2011/12 had the highest coverage with 1,528 reporting beekeepers (Table 1). As participation was voluntary and the data were recorded anonymously, it was not possible to track specific beekeeping operations across the years. Table 1 shows the number of reporting operations for each winter along with the total number of wintered and lost colonies and the relative proportion of lost colonies including a 95% confidence interval. Furthermore, the table shows that winter losses vary considerably from year to year ranging from 8.10% to 28.41%. The winters of 2011/12 and 2014/15 stand out with very high winter losses (26.01% and 28.41% respectively), whereas winter 2015/16 showed the lowest observed loss rate (8.10%) within the total observation period.
Lee et al.52 discussed the relevance of operation size and associated management factors (e.g. tendency for migratory beekeeping and the willingness or ability to treat bees for bee pests and diseases). Following Lee et al.52, beekeepers can be categorized as ‘backyard beekeepers’ (1–50 colonies), ‘sideline beekeepers’ (51–500 colonies) and ‘commercial beekeepers’ (more than 500 colonies) according to the number of colonies they have. They found that winter losses tend to be lower for commercial beekeepers than for backyard beekeepers. Our data contains observations from 6,223 backyard beekeepers, 430 sideline beekeepers and two commercial beekeepers. The average size of the observed beekeeping operations was approximately 19 colonies. Operations with more than 500 colonies are rare in Austria36; the largest beekeeping operation in our data set managed 580 colonies. Although Austrian commercial beekeepers generally have smaller colony numbers than their counterparts in the US, operation size is nevertheless assumed to be a risk factor associated with winter losses also in Europe38 and our model results (see below) confirm the importance of operation size for winter losses.
For each beekeeping operation, geographic information was available on the level of municipality. In order to guarantee the anonymity of beekeepers in the study at hand, data was collected on operation level37, whereas one operation could also have several apiaries. Therefore, it was not possible to exactly evaluate the land cover in the estimated flight range around each honey bee colony. The accuracy of the results depends on the assumption that the assignment of the apiaries to the clusters based on the available geographical information is correct. Furthermore, the observations do not follow a designed sampling plan, as the high number of observed colonies across Austria could only be ensured through a voluntary self-reporting system regarding wintering success. Representativeness can therefore not be guaranteed and the presence of a reporting bias can neither be ruled out nor quantified. Therefore, and also because honey bees forage on an area of up to 100 km2 (according to Couvillon & Ratnieks, 201553), the precise landscapes in which honey bees collect food cannot be determined. Furthermore, honey bees do not randomly forage over a landscape but exploit nested patches of forage due to their dance communication. The land cover in Austria is very heterogeneous at a small scale and the individual land use categories are highly correlated, see Supplementary Figures S1–S2. The grouping of individual land use categories into a manageable number of clusters removes the strong correlations that would otherwise impair the stability and interpretability of the statistical analysis. The hierarchical cluster analysis was hence used to assign each of the 263 regions of Austria into one of six clusters according to the proportional composition of the land use categories in the region. Clusters were identified such that regions in the same cluster are more similar regarding their land cover composition compared to regions from different clusters. Table 2 can be used to identify predominant land cover categories for each cluster. It contains the median relative area for each cluster and land cover category (in %). Figure 2 displays the spatial distribution of the six distinct clusters of land use within Austria. As clusters are characterised by the proportional composition of land use categories, these categories themselves cannot be assigned to one cluster exclusively. The cluster analysis rather defines weights, with which the categories are present in each cluster. This is illustrated by the composition of Cluster 2 (Table 2) which contains crop excl. maize (29.63%), broad-leaved forest (9.88%), other field crops (9.54%) and artificial surfaces (7.25%). Cluster 5 predominantly contains grassland (15.72%), coniferous forest (14.85%), maize (13.32%) and crop excl. maize (12.40%). In the remaining document, generated clusters will be referred to by their dominant land cover categories (i.e. categories with median values greater than 10%) to facilitate the identification of the most influential land use categories.
Cluster 1, which is dominated by wetland areas and crop excl. maize, covers only three of the 263 regions in Austria. Said regions are all located near major Austrian lakes (see Fig. 2): two of the regions are located near Lake Neusiedl (Burgenland), one region lies near Lake Constance (Vorarlberg). The geographic distribution of the three regions further demonstrates that spatial vicinity of regions did not in any way influence the generation of the clusters. Cluster 2 is dominated by crop cultivating areas. The predominant land use categories in Cluster 3 are artificial surfaces, broad-leaved forests and coniferous forests. The geographic distribution of the associated regions shows that these regions are located around major cities (Vienna, Linz, Graz, Klagenfurt), this explains the dominance of artificial surfaces in this cluster. Cluster 4, predominated by coniferous forest and grassland, comprises the largest number of regions. Cluster 5 includes many areas used for cultivating crop and maize as well as larger areas of grassland and coniferous forests. The regions that form Cluster 6 are mainly located in mountainous areas. The dominating land use categories in this cluster are semi-natural areas, coniferous forest and pastures. The cluster, however, does not contain any categories related to agricultural cultivation (median coverage of 0% for such categories, Table 2).
The study at hand aims at examining the relationship between the land use composition surrounding the location of bee colonies and honey bee winter losses. This was achieved by analysing the (statistical) influence of the landscape cluster in which colonies are located on the winter losses of the respective operation. Figure 3 provides a first descriptive univariate analysis of the winter loss rates across the clusters. The error bars indicate 95% confidence intervals for the proportion of lost colonies. The width of the error bars is an indicator of the number of observations per cluster/year, as the width of the confidence intervals decreases with increasing observation numbers. Cluster 1 shows exceptionally wide confidence intervals, especially in winters 2010/11, 2013/14 and 2014/15. In these years, the number of reporting operations in this cluster was between 1 and 6 only. The conspicuously high proportion of losses in 2010/11 is thus based on only one report from a single operation with 28 wintered and 12 lost colonies. The losses in 2014/15 are based on observations from six beekeepers, where two of them lost 100% and 86% of their wintered colonies, respectively. The high proportion of winter losses in this cluster is therefore subject to substantial uncertainty due to low sample size. In contrast, Cluster 4 comprises reports from between 313 and 697 operations per year. Based on the descriptive analysis in Fig. 3, no general trend can be identified over the years and no obvious categorisation into clusters with beneficial or detrimental landscape compositions for honey bee colony wintering success can be carried out holding true for all years.
Relation of land use and colony losses
Using a Generalised Linear Mixed Model, the cluster membership of the beekeeping operations was identified as a significant factor influencing their proportional winter losses. Apart from the cluster membership, operation size, the year of wintering and the interaction of year and cluster membership could be further established as significant factors. The significance of the interaction term indicates that the effect of one cluster may change over the years (e.g. higher winter losses in Cluster 6 compared to Cluster 4 for winter 2010/11, but lower winter losses in Cluster 6 compared to Cluster 4 for winter 2011/12). The model results are listed in Table 3. The estimate for winter losses of an average sized beekeeping operation in Cluster 4 and winter 2010/11 is 12.27%. Compared to Cluster 4, the odds for a winter loss increase by a factor of 2.083 for operations in Cluster 6 for this same winter. Model results further indicate that the risk of a winter loss significantly decreases with the number of wintered colonies. Note that, since the operation size was transformed for the modelling (centered by its mean and scaled by its standard deviation), it is not possible to directly interpret the parameter estimates for a one-unit-increase in operation size. The intercept represents the baseline for an average sized beekeeping operation (approximately 19 colonies). To compute the expected winter loss rates related to other operation sizes, one has to fall back on the transformed variable. The estimated probability for a winter loss for operations with 20 colonies is 12.23% and therefore 0.04% lower than for average sized operations. The probability for a beekeeper with approximately 59 colonies (small sideline beekeeper) is 10.79% and therefore 1.48% lower than for an average sized operation (backyard beekeeper)38.
To visualise the interaction effect of year and cluster membership, the predicted probabilities of a winter loss for an average sized beekeeping operation are shown in Fig. 4 in the form of a heat map. Darker colours indicate high probabilities for a winter loss, light colours indicate low probabilities. The values of the estimated probabilities and their 95% confidence intervals are further indicated in the respective tiles. The confidence intervals for the predictions were determined on the link scale using the normal approximation. Uncertainty of random parameters was not taken into account. Cluster 6, with mainly semi-natural areas, coniferous forests and pastures, shows the lowest winter loss probability over nearly all years. Only the winter of 2010/11 contradicts these results with relatively high winter losses in Cluster 6. The semi-natural areas forming Cluster 6 are mainly found in the western, mountainous parts of Austria. In this region we can expect the resource providing unit to show several differences to those in the rest of the country. Differences may relate to the intensity of agricultural use (including pesticide application)29,30, the forage diversity32,35,54 and climate42. It can be assumed that one of the aforementioned factors, or possibly the combination of all, could benefit the bees in semi-natural areas. To finally answer these questions, however, further georeferenced studies are necessary55.
Differences between clusters are higher for winters with generally high winter losses (2010/11, 2014/15). This might indicate that the surrounding landscape effects honey bee health especially in years with poor conditions for successful wintering such as high infestation levels with Varroa destructor. In years with very low winter losses, on the other hand, the spectrum to detect differences between diverging areas is narrow. The highest risk of winter losses is predicted for Cluster 1 in the years 2010/11 and 2014/15. The estimates for this cluster, which is dominated by wetland areas, are, however, based on very few observations from a low number of beekeepers. The descriptive analysis already showed high uncertainty. This is again reflected in the width of the confidence intervals in Fig. 4, especially for seasons 2010/11 and 2014/15. Results for this cluster must, therefore, be interpreted with caution. Cluster 3, which is characterized by artificial surfaces and forests, shows rather high probabilities for winter losses in most of the years. As was noted for Cluster 6, the results for season 2010/11 also contradict the results of the other reported winter seasons in Cluster 3. The number of observations that these results are based upon is, however, noticeably lower in this year compared to other years. This may challenge the reliability of the results, indicating a strong effect of individual years.
Contrary to what might have been expected from other studies17,19,20,25,29,30, Clusters 2 and 5, which comprise regions with relatively high proportions of arable land (Table 2), were not among the clusters with the highest risks of winter losses in most of the years (Fig. 4). Though most of these studies primarily focused on different pesticide treatments of agricultural crops, the general influence of agriculture on honey bee health is poorly studied12. It should be noted that in Clusters 2 and 5, arable land makes up less than half of the land cover. The heterogeneity of these clusters and the lack of information on whether the arable land was cultivated organically or conventionally did not allow an assessment of the use of pesticides, which is discussed as a risk factor for honey bee colony winter losses21. One explanation for our deviating findings could be the fact that agriculture in Austria is at a small scale compared to that of many other countries. This is also underlined by the heterogeneous composition of Clusters 2 and 5 (Table 2). The influence of such heterogeneous clusters on honey bee health is more difficult to interpret than that of more homogeneously composed clusters such as Cluster 6, which in total consists of more than 70% semi-natural areas, coniferous forest and pastures. Field studies, on the other hand, often face the problem of a limited sample size and the proof that control and exposure group experienced different treatments19,20,25. Likewise, our datasets lack information on pesticide usage not only for the INVEKOS dataset, so that no differentiation between the presumably dominant conventional and the less frequent organic farming is possible, but also for all other land use categories that could be contaminated to different extents. Honey bees can forage in large areas, and preferably visit attractive foraging areas53. The role of melliferous agricultural crops for honey bee health therefore deserves further research attention, as it applies to beneficial56 (plentiful resources during flowering) but also detrimental properties, such as reduced plant diversity57 and pesticide exposure, even by drift to neighbouring plants55.
As indicated by the significance of the interaction between year and cluster membership, winter losses in one cluster can be higher in one year and lower in another compared to other clusters. Similar effects were shown in Clermont et al.13, where cluster analysis was used to categorise the 2 km and 5 km radius, respectively, around honey bee apiaries according to land cover. Univariate tests for different years in their study revealed that, e.g., mixed woodland can have a positive impact on successful wintering in one year and a negative impact in other years. A controlled study reported in Alaux et al.54, comparing agricultural habitats to such enriched with melliferous catch crops, indicates that honey bee health, and thus successful wintering, hinges on the quantity and quality of food supply before wintering. According to another study that placed colonies in landscape dominated by agricultural cultivation, the amount and diversity of pollen available to honey bee colonies was found to be rather independent of landscape composition58. However, there is a general agreement that pollen supply is strongly influenced by seasonal variations32,33. Apart from the habitat surrounding the colony and forage availability, other factors are assumed to influence winter losses as well2,3,4,5,6. These are often related to hive management, but also to environmental factors such as weather42, colony density as a driver for pathogen spread59 or pesticides25,55. This complex interplay of influencing factors and landscape composition, including infestation level with the mite Varroa destructor60, could explain the strong effect of the year and the varying cluster effects over the years seen in our model results. As there might be different mechanisms, or combinations of mechanisms, effective in a year with high losses compared to a year with low losses, it might be promising to investigate more cases of high winter losses or extend the methodology applied to other countries.
As discussed in Clermont et al.13, the reference year of the collected land cover data is crucial for the reliability of the analysis. The data basis at hand is composed of three different data sources for land cover44,45,46. The BFW data set, which comprises information on forests in Austria, relies on observations from 2000–2003. Thus, observations regarding woodlands in Austria of 2000–2003 are used to explain winter losses from 2010 to 2015. The CORINE data set, which is mainly used to identify categories such as wetlands and artificial surfaces, was collated in 2012. Both, the BFW and CORINE data, are however assumed to be rather stable over the study period. The INVEKOS data, on the other hand, which characterises the agricultural land cover, is assumed to be volatile compared to the other data sources. This data was available on a yearly basis. Thus, the agricultural land cover in the spring of a year was indeed available to be used to explain the honey bee winter losses in the following winter. The large annual variability in winter loss rates of honey bee colonies experienced during the investigated years might therefore be rather caused by weather and other factors. Our study is a correlational analysis, thus preventing a clear causal explanation. Nevertheless, it facilitates discussions on which habitats are beneficial or disadvantageous for healthy honey bee colonies. In contrast to field studies on locations picked for testing the impact of agricultural versus non-agricultural landscapes or pesticide effects on honey bees, our epidemiological approach allows to investigate the impact of the mixed environments bees are confronted with in a heterogeneous landscape.
We could show that land cover did affect the honey bee winter colony mortality in Austria, as the estimated loss probability was lowest in regions composed mainly of semi-natural areas, coniferous forests and pastures in four out of six years compared to other regions. Moreover, we found significantly lower loss probabilities in these regions compared to regions predominantly composed of artificial surfaces, broad-leaved forest and coniferous forest in five out of six years. In addition to the land cover, the year of observation, the interaction between the year of wintering and cluster membership, and operation size had significant effects on the winter mortality. This suggests that other factors in addition to landscape composition might be responsible for high winter losses in individual years. It also indicates that conclusions drawn from analyses of a single winter should be interpreted with great caution, and further long-term studies are needed to understand honey bee colony losses.
The data regarding the winter losses are not publicly available to preserve the privacy of participants; however they are available from the authors upon reasonable request. The INVEKOS and BFW data are available from the Austrian Federal Ministry of Agriculture, Forestry, Environment and Water Management and the Austrian Research Centre for Forests, respectively, but restrictions apply to the availability of these data, which were used under license for the current study, and so are not publicly available. Data are however available from the authors upon reasonable request and with permission of the aforementioned third parties. The CORINE land cover data are publicly available from the European Environment Agency.
van Engelsdorp, D. et al. A national survey of managed honey bee 2010–11 winter colony losses in the USA: results from the Bee Informed Partnership. J. Apic. Res. 51, 115–124 (2012).
van der Zee, R. et al. Managed honey bee colony losses in Canada, China, Europe, Israel and Turkey, for the winters of 2008–9 and 2009–10. J. Apic. Res. 51, 100–114 (2012).
van der Zee, R. et al. Results of international standardised beekeeper surveys of colony losses for winter 2012–2013: Analysis of winter loss rates and mixed effects modelling of risk factors for winter loss. J. Apic. Res. 53, 19–34 (2014).
Liu, Z. et al. Survey results of honey bee (Apis mellifera) colony losses in China (2010–2013). J. Apic. Res. 55, 29–37 (2016).
Seitz, N. et al. A national survey of managed honey bee 2014–2015 annual colony losses in the USA. J. Apic. Res. 54, 292–304 (2016).
Döke, M. A., Frazier, M. & Grozinger, C. M. Overwintering honey bees: Biology and management. Curr. Opin. Insect Sci. 10, 185–193 (2015).
Goulson, D., Nicholls, E., Botías, C. & Rotheray, E. L. Bee declines driven by combined stress from parasites, pesticides, and lack of flowers. Science 347, 1255957 (2015).
Potts, S. G. et al. Safeguarding pollinators and their values to human well-being. Nature 540, 220–229 (2016).
Steinhauer, N. et al. Drivers of colony losses. Curr. Opin. Insect Sci. https://doi.org/10.1016/j.cois.2018.02.004 (2018).
Carré, G. et al. Landscape context and habitat type as drivers of bee diversity in European annual crops. Agric. Ecosyst. Environ. 133, 40–47 (2009).
De Palma, A. et al. Predicting bee community responses to land-use changes: Effects of geographic and taxonomic biases. Sci. Rep. 6, 31153 (2016).
EFSA Panel on Animal Health and Welfare (AHAW). Assessing the health status of managed honeybee colonies (HEALTHY-B): a toolbox to facilitate harmonised data collection. EFSA J. 14, e04578 (2016).
Clermont, A., Eickermann, M., Kraus, F., Hoffmann, L. & Beyer, M. Correlations between land covers and honey bee colony losses in a country with industrialized and rural regions. Sci. Total Environ. 532, 1–13 (2015).
Lundin, O., Rundlöf, M., Smith, H. G., Fries, I. & Bommarco, R. Neonicotinoid Insecticides and Their Impacts on Bees: A Systematic Review of Research Approaches and Identification of Knowledge Gaps. PLoS one 10, e0136928 (2015).
Blacquière, T. & van der Steen, J. J. M. Three years of banning neonicotinoid insecticides based on sub-lethal effects: can we expect to see effects on bees? Pest Manag. Sci. 1299–1304, https://doi.org/10.1002/ps.4583 (2017).
Blacquière, T., Smagghe, G., van Gestel, C. A. M. & Mommaerts, V. Neonicotinoids in bees: a review on concentrations, side-effects and risk assessment. Ecotoxicology 21, 973–992 (2012).
Simon-Delso, N. et al. Honeybee Colony Disorder in Crop Areas: The Role of Pesticides and Viruses. PLoS one 9, e103073 (2014).
Wu-Smart, J. & Spivak, M. Sub-lethal effects of dietary neonicotinoid insecticide exposure on honey bee queen fecundity and colony development. Sci. Rep. 6, 32108 (2016).
Pilling, E., Campbell, P., Coulson, M., Ruddle, N. & Tornier, I. A Four-Year Field Program Investigating Long-Term Effects of Repeated Exposure of Honey Bee Colonies to Flowering Crops Treated with Thiamethoxam. PLoS one 8, e77193 (2013).
Hoppe, P. P. et al. Effects of a neonicotinoid pesticide on honey bee colonies: a response to the field study by Pilling et al. (2013). Environ. Sci. Eur. 27, 28 (2015).
Budge, G. E. et al. Evidence for pollinator cost and farming benefits of neonicotinoid seed coatings on oilseed rape. Sci. Rep. 5, 12574 (2015).
Rolke, D., Fuchs, S., Grünewald, B., Gao, Z. & Blenau, W. Large-scale monitoring of effects of clothianidin-dressed oilseed rape seeds on pollinating insects in Northern Germany: effects on honey bees (Apis mellifera). Ecotoxicology 25, 1648–1665 (2016).
Schmuck, R. & Lewis, G. Review of field and monitoring studies investigating the role of nitro-substituted neonicotinoid insecticides in the reported losses of honey bee colonies (Apis mellifera). Ecotoxicology 25, 1617–1629 (2016).
Smart, M., Pettis, J., Rice, N., Browning, Z. & Spivak, M. Linking Measures of Colony and Individual Honey Bee Health to Survival among Apiaries Exposed to Varying Agricultural Land Use. PLoS one 11, e0152685 (2016).
Woodcock, B. A. et al. Country-specific effects of neonicotinoid pesticides on honey bees and wild bees. Science 356, 1393–1395 (2017).
Tsvetkov, N. et al. Chronic exposure to neonicotinoids reduces honey bee health near corn crops. Science 356, 1395–1397 (2017).
Alburaki, M. et al. Neonicotinoid-coated Zea mays seeds indirectly affect honeybee performance and pathogen susceptibility in field trials. PLoS one 10, e0125790 (2015).
Alburaki, M. et al. Performance of honeybee colonies located in neonicotinoid-treated and untreated cornfields in Quebec. J. Appl. Entomol. 141, 112–121 (2017).
Alburaki, M. et al. Agricultural Landscape and Pesticide Effects on Honey Bee (Hymenoptera: Apidae) Biological Traits. J. Econ. Entomol. 110, 835–847 (2017).
Alburaki, M. et al. Landscape and pesticide effects on honey bees: forager survival and expression of acetylcholinesterase and brain oxidative genes. Apidologie 48, 556–571 (2017).
Brodschneider, R. & Crailsheim, K. Nutrition and health in honey bees. Apidologie 41, 278–294 (2010).
Donkersley, P., Rhodes, G., Pickup, R. W., Jones, K. C. & Wilson, K. Honeybee nutrition is linked to landscape composition. Ecol. Evol. 4, 4195–4206 (2014).
Di Pasquale, G. et al. Variations in the Availability of Pollen Resources Affect Honey Bee Health. PLoS one 11, e0162818 (2016).
Omar, E. et al. Influence of different pollen diets on the development of hypopharyngeal glands and size of acid gland sacs in caged honey bees (Apis mellifera). Apidologie 48, 425–436 (2017).
Lecocq, A., Kryger, P., Vejsnæs, F. & Bruun Jensen, A. Weight Watching and the Effect of Landscape on Honeybee Colony Productivity: Investigating the Value of Colony Weight Monitoring for the Beekeeping Industry. PLoS one 10, e0132473 (2015).
Brodschneider, R., Moosbeckhofer, R. & Crailsheim, K. Surveys as a tool to record winter losses of honey bee colonies: a two year case study in Austria and South Tyrol. J. Apic. Res. 49, 23–30 (2010).
van der Zee, R. et al. Standard survey methods for estimating colony losses and explanatory risk factors in Apis mellifera. J. Apic. Res. 52, 1–36 (2013).
Brodschneider, R. et al. Preliminary analysis of loss rates of honey bee colonies during winter 2015/16 from the COLOSS survey. J. Apic. Res. 55, 375–378 (2016).
Jacques, A. et al. A pan-European epidemiological study reveals honey bee colony survival depends on beekeeper education and disease control. PLoS one 12, e0172591 (2017).
van der Zee, R., Gray, A., Pisa, L. & Rijk, T. de. An Observational Study of Honey Bee Colony Winter Losses and Their Association with Varroa destructor, Neonicotinoids and Other Risk Factors. PLoS one 10, e0131611 (2015).
Brodschneider, R. & Crailsheim, K. Fünf Jahre Untersuchung des Bienensterbens in Österreich. Entomol. Austriaca 20, 195–205 (2013).
Switanek, M., Crailsheim, K., Truhetz, H. & Brodschneider, R. Modelling seasonal effects of temperature and precipitation on honey bee winter mortality in a temperate climate. Sci. Total Environ. 579, 1581–1587 (2017).
Zentralanstalt für Meterologie und Geodynamik (ZAMG). Jahrbuch — ZAMG. Available at: https://www.zamg.ac.at/cms/de/klima/klimauebersichten/jahrbuch. (Accessed: 25th January 2017).
AgrarMarkt Austria. Mehrfachantrag Flächen. (AgrarMarkt Austria, 2015). Available at: https://www.ama.at/getattachment/7bc4fd76-f8f2-40c5-80c0-eccf068413bb/MFA-Fl-2015-Juni-mobile.pdf (Accessed: 25th January 2017).
Austrian Research Centre for Forests BFW. Waldlayer Österreich – BFW. Available at: https://bfw.ac.at/db/bfwcms.web?dok=7222. (Accessed: 25th January 2017).
European Environment Agency EEA. CORINE land cover (1995).
James, G., Witten, D., Hastie, T. & Tibshirani, R. An Introduction to Statistical Learning. 103, (Springer, 2013).
Bilder, C. R., Zhang, B., Schaarschmidt, F. & Tebbs, J. M. binGroup: A Package for GroupTesting. R J. 2, 56–60 (2010).
R Core Team. R: A Language and Environment for Statistical Computing. (R Foundation for Statistical Computing, 2016).
Bates, D., Mächler, M., Bolker, B. & Walker, S. Fitting Linear Mixed-Effects Models Using lme4. J. Stat. Softw. 67 (2015).
Wickham, H. ggplot2 – Elegant Graphics for Data Analysis (Springer, 2009).
Lee, K. V. et al. A national survey of managed honey bee 2013–2014 annual colony losses in the USA. Apidologie 46, 292–305 (2015).
Couvillon, M. J. & Ratnieks, F. L. W. Environmental consultancy: dancing bee bioindicators to evaluate landscape “health”. Front. Ecol. Evol. 3 (2015).
Alaux, C. et al. A ‘Landscape physiology’ approach for assessing bee health highlights the benefits of floral landscape enrichment and semi-natural habitats. Sci. Rep. 7, 40568 (2017).
Simon-Delso, N., San Martin, G., Bruneau, E., Delcourt, C. & Hautier, L. The challenges of predicting pesticide exposure of honey bees at landscape level. Sci. Rep. 7 (2017).
Sponsler, D. B. & Johnson, R. M. Honey bee success predicted by landscape composition in Ohio, USA. PeerJ 3, e838 (2015).
Vaudo, A. D., Tooker, J. F., Grozinger, C. M. & Patch, H. M. Bee nutrition and floral resource restoration. Curr. Opin. Insect Sci. 10, 133–141 (2015).
Danner, N., Keller, A., Härtel, S. & Steffan-Dewenter, I. Honey bee foraging ecology: Season but not landscape diversity shapes the amount and diversity of collected pollen. PLoS one 12, e0183716 (2017).
Youngsteadt, E., Appler, R. H., López-Uribe, M. M., Tarpy, D. R. & Frank, S. D. Urbanization Increases Pathogen Pressure on Feral and Managed Honey Bees. PLoS one 10, e0142031 (2015).
Dolezal, A. G., Carrillo-Tripp, J., Miller, W. A., Bonning, B. C. & Toth, A. L. Intensively Cultivated Landscape and Varroa Mite Infestation Are Associated with Reduced Honey Bee Nutritional State. PLoS one 11, e0153531 (2016).
This research was conducted within the project “Zukunft Biene” (grant number: 100972) funded by the Austrian Federal Ministry of Agriculture, Forestry, Environment and Water Management.
The authors declare no competing interests.
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Kuchling, S., Kopacka, I., Kalcher-Sommersguter, E. et al. Investigating the role of landscape composition on honey bee colony winter mortality: A long-term analysis. Sci Rep 8, 12263 (2018). https://doi.org/10.1038/s41598-018-30891-y
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