Wild bee distribution near forested landscapes is dependent on successional state

Katherine A.Odanaka and Sandra M.Rehan*

Abstract

Keywords: Pollinator, Forest margin,Bee habitat, Nesting biology,Wild bees

Background

Within the past 10 years, our collective knowledge regarding the biology, behavior, and evolutionary history of wild bees has greatly expanded. As central place foragers, bees are highly dependent on the availability of resources near their nest and without access to acceptable forage or nesting risk extirpation from these environments (Greenleaf et al. 2007; Williams and Kremen 2007; Ferreira et al. 2013; Blaauw and Isaacs 2014). Human mediated environmental change is now a constant process and modifications in land use, especially agricultural expansion, are among the most damaging to wild bee communities, as former habitat and nesting resources are converted to pasture and farm land(Williams and Kremen 2007; Quintero et al. 2009;M’Gonigle et al. 2015; Newbold et al. 2015; Mallinger et al. 2016; Harrison et al. 2017). However, there are contrasting reactions by different bee communities to the varied types of landscape modification (such as but not limited to urbanization, agricultural expansion, or setting aside land for conservation) indicating that wild bees are responding to landscape level changes in local resources (Kremen et al. 2002; Bengtsson et al. 2005;Morandin and Winston 2005;Williams and Kremen 2007;Potts et al. 2010; Power and Stout 2011; Winfree et al.2011; Senapathi et al. 2015; Tucker and Rehan 2018).Furthermore, these varied reactions are largely dictated by biological traits (Biesmeijer et al. 2006; Williams et al. 2010; Bartomeus et al. 2013; Tucker and Rehan 2018) and certain traits for nesting (stem and cavity)and behavior (cleptoparasitism) constrain certain bee guilds to specific environments (Tscharntke et al. 1998;Sheffield et al. 2013).

Forested environments, including forest margins, provide ample resources that bees may not find in agriculturally intensive areas. This includes spring foraging sources, such as understory flowers and herbaceous plants, as well as nesting habitats in tree cavities and dead broken sticks and in bare ground (Aizen and Feinsinger 1994; De Marco and Coelho 2004; Taki et al.2007; Winfree et al. 2007; Farwig et al. 2009; Taki et al.2013; Bailey et al. 2014; Hanula et al. 2015; Joshi et al.2016). Additionally, forests and forest margins provide many important ecosystem services, including the exportation of beneficial arthropods into surrounding areas(Decocq et al. 2016). Prior research has indicated that farms located close to forest margins have increased pollination and yield as they benefit from the movement of bees and other pollinators from the forest environment to the farms in search of forage (Blanche et al. 2006;Mitchell et al. 2014). The effect of forests and other seminatural areas exporting these critical pollination services has been shown in both tropical (Ricketts 2004;Ferreira et al. 2015) and temperate regions (Watson et al. 2011; Schüepp et al. 2013; Bailey et al. 2014). Furthermore, as distance from forest margins increases, pollination and yield on farms decrease, demonstrating how forest margins influence pollinator contribution near agricultural landscapes (De Marco and Coelho 2004;Chacoff and Aizen 2006; Carvalheiro et al. 2010; Mitchell et al. 2014). Although bees are known to be capable of flying hundreds of meters (Gathmann & Tscharntke 2002), this may be an exception as bees were found to forage much closer to their nests despite having large foraging distances (Zurbuchen et al. 2010a, 2010b). If this is the case, subtle differences in where bees distribute themselves from a forest edge could be detected at finer scales, yet this remains largely unexplored.

Although forests and forest margins remain an important resource for wild bees, not all forested environments are able to support abundant and diverse bee communities, and this largely depends upon the stage of succession it is currently in. Research has focused on either the early or late stages of forest succession and those phases that lie in between have often been ignored.Mature forests(late stage succession), characterized by old growth and containing closed canopies, are less favorable to bees than forests in earlier stages of succession (Taki et al. 2007;Swanson et al. 2011; Hanula et al. 2015). These earlier successional stages, which emulate the grassland habitats favorable for bees, are critical for the survival of solitary native bee populations as they provide essential floral resources and nesting habitat (Taki et al. 2013; Hanula et al.2015;Roberts et al.2017).Environments that are able to maintain states of early forest succession, through various means such as fires, grazing, or management will often have a more diverse and abundant native bee population (Potts et al. 2003a, b; Rubene et al. 2015; Kimoto et al. 2012; Noy-Meir 1995; Vulliamy et al. 2006). As forests continue to age and mature, shifts in the bee community occur and are dictated by various functional traits such as their behavior or nesting;solitary species give way to social species and ground nesters decline overall (Taki et al.2013; Hanula et al. 2015; Rubene et al. 2015). However,little is currently known regarding how forests in the midstage of succession affect wild bee populations or the extent of how functional traits dictate where wild bees distribute themselves across these mid successional stages.

Wild bee populations continue to decline while knowledge of their habitat requirements remain poorly documented (Winfree 2010; Burkle et al. 2013; Kerr et al.2015), resulting in a need for understanding how forest successional stages influence and shape bee communities. Deeper insight into the effects of forest succession and habitat requirements can ultimately inform different agricultural management schemes that can double as a means of wild bee conservation. We examined the effects of four unique stages of forest succession in order to 1) investigate the effects of successional stage and distance from forest margins on wild bee abundance and richness, 2) identify how nesting and behavioral traits create specificity for wild bee species in different successional stages, and 3) describe the wild bee community in New England forest systems for the first time.

Methods

Study sites and sampling

This study was conducted in Strafford County, New Hampshire (43.2383° N, 71.0236° W). Collection locations were in and around mixed eastern hemlock (Tsuga canadensis) and white pine (Pinus strobus) forests. Wild bees were sampled every 2 weeks starting the first week in May through the end of September 2017. Four different forest successional stages (clear-cut=forest after disturbance; closed canopy=pine and hemlock mixed forest with no canopy gaps; pasture=initial plant colonization of the gap; silvopasture=pine only and canopy gaps between trees), were surveyed including: closed canopy forest, clear-cut where trees had been completely removed with 0% canopy cover, silvopasture where selected trees were removed to allow 30% canopy cover for cattle to graze between the remaining trees, and pasture adjacent to forests. Both the clear-cut and silvopasture were created in 2015. Each rectangular site was approximately 1 hectare in area and all had at least one edge that was shared with the surrounding closed canopy forest. Pastures were mowed monthly and had no canopy cover. Ten cows were released at each of the pasture, silvopasture and clear-cut biweekly (alternating weeks to bee collection). Each site represented one successional stage and had three replicate 120 m transects;one of each transects were located at 10, 20, and 30 m from forest edges into each site. These transects were standardized to the forest edge so that 10, 20, or 30 m from the forest edge was the same distance regardless of the successional type.

We collected bees using colored pan traps that were either blue, white, or yellow following standard procedure(Tucker and Rehan 2016; 2018). We placed twelve pan traps (7-cm diameter, 100 mL) alternating in blue, white,yellow pattern on the ground along each 120-m transect allowing for 10 m between each cup and filled each one with soapy water. Traps were deployed before 8 AM and were collected the same day after 4 PM, allowing for a total of 8 h collection.When emptying pan traps,contents of each trap were poured through a sieve and any collected specimens were placed in a vial containing 70%ethanol and a collection tag. Additionally, we recognize that pan traps have been shown to be biased against social and larger bee species, and are particularly favorable to those in the Halictidae(Droege et al.2010).

Bee identification

Following the protocols in Droege (2015) we washed bee specimens and dried them with a hair drier. Once dry,specimens were then pinned, labeled with relevant location information and a unique QR code, and identified to species using online keys found on Discover Life(http://www.discoverlife.org/) as well as previously published taxonomic keys (Mitchell 1960, 1962; Gibbs 2011;Rehan and Sheffield 2011; Gibbs et al. 2013; all specimens are housed in the Rehan Lab at York University).After identification, we grouped species by their behavior type (social, solitary, cleptoparasitic) and their nesting biology (ground, stem). Bees that were classified as preferring only cavities or alternating between stems and cavities were grouped into the stems category. For behavior, bees exhibiting communal behavior were grouped into the solitary category (Matteson et al. 2008;Ascher et al. 2014; Selfridge et al. 2017). A list of all bees in this study, including their behavior and nesting biology, can be found in the supplement (S1).

Statistical analyses

Similarity coefficients and initial rarefactions were completed for each of the successional states to determine sampling adequacy (S2, S3). We then used generalized linear mixed models with negative binomial distribution to analyze the effects of forest distance and successional type on wild bee abundance and richness (Zuur et al.2007). Both collection month and distance nested within site were used as random effect variables in our models.Fixed variables included site, distance from the forest edge, behavior type, and nesting biology. Analyses of deviance using type II Wald chi square tests were then conducted on our models in order to test for overall significance of treatments; followed by post hoc Tukey tests. All statistical analyses were conducted using R ver.(3.5.2) (R Core Team) and the packages ‘multcomp’(Hothorn et al. 2008), iNEXT (Chao et al. 2014; Hsieh et al. 2016), vegan (Oksanen et al. 2013) and lme4 (Bates et al. 2015).

Results

A total of 297 bees, representing 63 species and 18 genera were collected. The clear-cut maintained the highest total wild bee abundance (mean±SD; n=114±14.5),followed by the silvopasture (n=89±13.0), then the pasture (n=82±14.3), and finally the forest (n=12±2.7).When successional states were examined individually,the clear-cut, silvopasture, and pasture all had significantly higher bee abundance than the forest (Χ2=33.85,df=3, p ≤0.001).

Succession stage (forest, pasture, silvopasture, clear-cut)

Overall, species abundance differed significantly among successional stage and distances from the forest edge(Χ2=543.85, df=6, p ≤0.001; Fig.1a). The clear-cut (z=3.321; p=0.005), silvopasture (z=5.021; p ＜0.001), and pasture (z=4.481; p ＜0.001) all show significantly more wild bee abundance than the forest but are not different from each other. Additionally, there were significant differences in species abundance between 20 and 30 m(z=-22.39; p ＜0.001) as well as between 10 and 30 m(z=-19.46; p ＜0.001).

Bee species richness also differed significantly among successional states (Χ2=30.8, df=3, p ≤0.001),but not by distance (Χ2=0.05, df=2, p=0.975).Clear-cut (z=5.470; p ＜0.001), silvopasture (z=4.230;p ＜0.001), and pasture (z=4.498; p ＜0.001) were all significantly richer than the forest, but there was no difference in richness among the former three states.The clear-cut had the highest overall species richness(n=38±5.3), the pasture and silvopasture maintained equal amounts of species richness (pasture: n=32±6.4; silvopasture: n=32±13.0), while the forest had the least species richness (n=9±1.9). Species richness significantly varied among successional state by distance (Χ2=456.47 df=6, p ≤0.001; Fig.1b).

The interaction of succession type and bee behavior on wild bee abundance was significant (Χ2=15.44, df=6, p=0.02; Fig.2a). We found that solitary (z=5.15; p ＜0.001) and social (z=4.82; p ＜0.001) species were more abundant than cleptoparasitic species. No cleptoparasites were found at the forest. Overall,solitary bees were most abundant (n=164±26.8), followed by social bees (n=122±18.1), then cleptoparasites (n=11±2.3). Individuals from solitary species were most common in the pasture (n=62±12.5) and least common in the forest(n=7±2.1). The number of solitary individuals collected was second and third highest in the clear-cut and silvopasture respectively (clear-cut: n=58±7.4; silvopasture:n=37±6.5). Social bees were most common in the clear-cut (n=51±8.5) and least common in the forest(n=5±0.7). The silvopasture had more social individuals (n=49±8.2) than the pasture (n=17±5.4). Cleptoparasitic individuals were most frequent in the clear-cut sites (n=5±1). Cleptoparasitic bees were equally collected within the pasture and silvopasture sites(n=3±0.9).

The effect of species behavior on overall richness was significant (Χ2=60.4; df=2, p ＜0.001; Fig.2b). Total richness among behavioral categories indicated that solitary bees were the most species rich (n=32±6.4). Species richness of cleptoparasitic bees was almost as high as social species (n=11±2.3 and n=20±4.1 respectively). Across four different successional states, solitary bees were most diverse in the clear-cut (n=21±3.7)with far fewer species collected in the forest (n=5±1.6).The pasture sites were the second highest in solitary bee richness (n=21±4.7) and this was followed by the silvopasture sites (n=15±1.8). Social bee richness was highest in the silvopasture sites (n=14±2.3), followed by clear-cut (n=12±2.5), then pasture (n=8±1.9), and fewest in the forest sites (n=4±0.4). The clear-cut sites had the most cleptoparasite species (n=5±0.45). The pasture and silvopasture sites (n=3±0.4) each had cleptoparasitic species, and the forest had no observed cleptoparasites.

Overall, ground nesters were more abundant (n=202±28.5) than stem nesters (n=95±16.1; Χ2=27.88;df=1; p ≤0.001). Successional state (forest, pasture, silvopasture, clear-cut) was also found vary significantly among nesting biologies (Χ2=27.11; df=3; p ＜0.001;Fig.3a). Ground (n=76±10.3) and stem (n=38±5.5)nesting individuals were most abundant in the clear-cut sites. Abundance of ground and stem nesters (n=59±8.61, n=30±5.0 respectively) were second highest in the silvopasture sites. In the pasture sites,ground nesters(n=58±9.4) comprised 71% of the bees captured and the remaining 29% were stem nesters (n=24±5.4).Three quarters (75%) of the individuals collected from the forest sites were ground nesters (n=9±1.5) and the remaining 25%were stem nesters (n=3±1.3).

Species richness varied significantly between nesting biology categories (Χ2=27.34, df=1, p ≤0.001; Fig.3b).Overall, ground nesting bees had higher species richness than stem nesters (n=45±6.8 and n=19±4.9 respectively; Χ2=27.34, df=1, p ≤0.001). At the successional state level, ground nesters were most species rich within clear-cut sites (n=28±4.2), followed by the pasture and silvopasture sites (n=23±4.2, n=21±2.5 respectively).The forest sites had the least ground nesting species richness (n=7±1.4). Species richness of stem nesting bees was highest in both the clear-cut and silvopasture sites (clear-cut: n=10±2.3; silvopasture: n=11±1.2).The pasture sites contained the third highest (n=9±2.44) and the forest sites had the least number of species(n=2±0.9).

Distance

When examined together, the effects of distance on total bee abundance (both ground and stem nesters) was not significant (Χ2=0.524, df=2, p=0.77). However, there was a significant interaction between nesting biology and distance to forest margins (Χ2=10.18; df=2; p ＜0.006; Fig.4a). Ground nesting bee abundance increased about 36% from 10 to 20 m and remained constant at 30 m. For stem nesters, bee abundance was highest at 10 m and significantly lower at 20 m.At 30 m,stem nesting bee abundance is significantly higher than abundance at 20 m, but also lower than bee abundance at 10 m. Interactions between distance and nesting biology were significant (Χ2=6.64, df=2, p=0.04; Fig.4b).Ground nesting bees increased by 56% in species richness from 10 to 20 m and remained consistently high at 30 m away from forest margins. Stem nesters had a significant difference in species richness at 20 m from forest margins (z=-3.164; p=0.002).

Each distance was also found to have specific bee species. Of 63 bee species, 33 (52%) were only found at certain distances from the forest margin (Table 1). Most of the distance specific species were found 30 m from forest margins (n=15) and the least were found closest to forest margins at 10 m transects (n=7). Of the total distance specific bees, 81% were found to be ground nesters (n=27) and six of these species, all in the genus Lasioglossum, were found to be social. Half of all distance specific species were members of the family Halictidae and of those 18 species, nine occurred solely 30 m from forest margins. These include the only Augochlora species (A. pura) and the only Agapostemon species (A.sericeus) found solely at 30 m from forest margins. In total, 12 of the 18 (67%) species from the family Halictidae were from the genus Lasioglossum. Half of those Lasioglossum species (n=6) were collected 20 m from forest margins and those species comprised 46% of the total specific species to that distance. Additionally, the only Anthidium species (A. manacatum) found in this study was captured at 20 m from a forest margin. Although transects 10 m from the forest margin contained the least specific species these include the lone specimens of Hoplitis (H. spoliata) and Melissodes (M.druriellus).

Successional state specificity

Three species were collected in all four successional states: Agapostemon virescens, Calliopsis antenniform,and Lasioglossum coriaceum. Conversely, each successional state was found to have species not collected in the other sites. In total, 34 of the 63 (54%) bee species collected in this study were present in only one of the four successional states (Table 2). The clear-cut and pasture both contained the highest number of stage specific species (n=11). The clear-cut contained the most halictid species, the only species of Augochlora (A. pura), and Anthidium (A. oblongatum) found in this study. Thepasture contained the most species of the family Megachilidae captured in one site (n=4). Included in these four species were the only species of Hoplitis (H. spoliata), the only Megachile (M. companulae, M. latimanus), and one Osmia (O. albiventris) species.Furthermore, the only Melissodes (M. druriellus) was found at a pasture site.

Table 1 Species specific to distances from forest edge. Species include five bee families (bold)and 11 genera.Nesting biology indicated with:*=ground nesting, and Δ=stem/cavity nesting species. Social behavior indicated in parentheses with:(sol)=solitary,(soc)=social, and (par)=cleptoparasitic species

Although the forest and silvopasture both are comprised of mixed forest, they did not have any similarities in community composition or number of stage-specific species. Only two species were found only in the forest:Andrena nigrihirta and Lasioglossum pilosum. The silvopasture however, contained ten stage-specific species,half of which were Lasioglossum species, which was the most for any successional stage and includes L.platyparium, the only social parasitic species of this genus collected in this study. The silvopasture sites also contained the most successional state specific Osmia (n=2) species: O. atriventris and O. collinsiae.

Discussion

This study investigated and documented the effects of four different successional states and three different distances from forest margins on wild bee communities.Here we determined successional stage specificity among wild bees as a product of set traits such as species behavior and nesting biology. Our study reveals that wild bees in forested environments are affected by distance from forest margins and by nesting habitat. Within each successional state, we found bees assorted by their behavior and nesting biology while nesting biology alone revealed different niches at 10 versus 20 and 30 m from forest margins. Findings from our study further support the need for heterogeneous landscape composition to bolster diverse wild bee communities.

Succession type (forest, pasture, silvopasture, clear-cut)

Wild bee behavior and nesting biology was significantly associated with successional state. We found thatenvironments containing little to no canopy cover supported the most abundant and rich bee communities in comparison to the forest dominated by dense stands of trees which is consistent with previous findings (Winfree et al. 2007; Hanula et al. 2015; Roberts et al. 2017).Dense forests lack many of the resources important for bee habitat, such as nesting substrate, suitable sunlight,and consistent forage (Swanson et al. 2011; Hanula et al.2015, 2016). This is especially critical once the spring blooming period has ended and trees begin to produce leaves which block sunlight from reaching the understory and prohibit the growth of additional forage (Taki et al. 2007; Schüepp et al. 2013). Moreover, foraging by bees and other hymenopterans is reduced in the presence of shade and thus cooler temperatures (Herrera 1995; McKinney and Goodell 2010; Polatto et al. 2014).The majority of wild bees found in the forest were solitary ground nesters and were located close to forest margins. This observation provides evidence further supporting the notion that solitary bees will build their nests at forest edges where there is less canopy shade and more open ground(Klein et al. 2003).

Table 2 Species specific to the four different successional states examined in this study. Species include five bee families (bold) and 11 genera.Nesting biology indicated with:*=ground nesting, and Δ=stem/cavity nesting species. Social behavior indicated in parentheses with:(sol)=solitary, (soc)=social,and (par)=cleptoparasitic species

The pasture, clear-cut, and silvopasture states all represent different stages of deforestation allowing for insight into how wild bee populations respond to disturbance.Previous research has shown that bees respond favorably to disturbance from forested environments and will be found consistently in greater numbers where disturbance has occurred (Hanula and Horn 2011;Fiedler et al. 2012; Hudson et al. 2013). The most disturbed of our states studied were the clear-cut sites,which maintained the highest bee community abundance and species richness in this study. Since disturbance reverts sections of forest back to early stage succession, our clear-cut sites may be able to generate an abundance of essential foraging and nesting resources, which are essential for attracting and retaining populations of solitary bees (Taki et al. 2013; Roberts et al. 2017).Local factors,such as the availability of nesting resources, can impact wild bee community composition by increasing species diversity (Murray et al. 2012)which can explain the highly taxon and habitat specific differences in the wild bee communities found between our silvopasture and pasture sites. Both silvopasture and pasture sites had nearly equal richness and abundance of wild bees, but each successional state provided habitat to different species based on nesting biology and behavior.Where the pasture sites contained more bare ground and thus catered more towards solitary ground nesting bees, the silvopasture, which lacked exposed soil, housed more stem nesting bees and more species exhibiting social behavior.

Distance

Our results indicate that the overall distribution of wild bees across different distances near forest margins is determined by nesting biology and perhaps the availability of specific nesting resources. Bailey et al. (2014) found that distance from the forest margin was one of the most important factors in explaining variance in wild bee communities. We found that distance from forest margins explained differences in bee abundance and richness only when the community was grouped by nesting guild.Stem nesting bees were mostly found at 10 m, while ground nesting species were much more common at 20 and 30 m from forest margins. These variances were likely due to the location of appropriate nesting substrate, as stems and twigs were most abundantly located closest to forest margins, while exposed bare ground increased as distance from forests increased. Furthermore,our results support research by Cane et al. (2006) and Potts et al. (2003a, b, 2005), who suggest that the availability of nesting resources exert enough pressure to shape bee communities based on their specific nesting guilds.

The effect of distance from forest margins on wild bee communities is a topic of increasing interest, especially in regards to agriculture; yet very few of these distance studies detail changes in specific bee species as distance from forest margins increase (Chacoff and Aizen 2006;Taki et al. 2007; Bailey et al. 2014; Joshi et al. 2016).Many of these studies are in agriculture settings and show overall declines in species richness and floral visitation rates as distance increases (Klein et al. 2003;Kohler et al. 2008; Carvalheiro et al. 2010; Schüepp et al.2013). Unlike earlier distance studies, whose maximum distance from the forest edge was 100 m or more (Taki et al. 2007; Watson et al. 2011; Bailey et al. 2014; Joshi et al. 2016), the spatial scale of our project was much finer, focusing on 10 to 30 m. This reduced scale allows us to detect narrower nuances in the distribution of wild bees across shorter distances and examine how species composition changes as distance increases. We found that over half of recorded bee species were distance specific and that distance specificity is a product of bee nesting biology. Our conclusion further corroborates the notion that nesting resources are able to shape bee communities (Potts et al. 2005; Cane et al. 2006), but our result suggest this might occur at a much finer scale.Unlike nesting biology, we did not detect clear distance specificity among behavioral categories. Prior distance analyses that differentiate between the bee behavior classes focus mainly on honey bees or bumble bees or both as social representatives (Bailey et al. 2014; Joshi et al.2016). Consequently, little is currently known regarding the responses of social species outside of the Apidae,such as those in the genus Lasioglossum, to distances from forest margins.Future studies documenting all species are needed, especially to gain insights into the habitat requirements of the greatly understudied social halictids and the wide range of speciose solitary bees.

Successional state specificity

Our results corroborate previous findings regarding the importance of heterogeneous landscapes for diverse wild bee populations in larger ecosystems, especially agroecosystems where homogeneous landscapes are common(Steckel et al. 2014; Mallinger et al. 2016; Tucker and Rehan 2018). Both Tucker and Rehan (2018) and Svensson et al. (2000) found that landscape specificity affects species within genera differently and our results mirror those findings. This effect can best be seen in the genus Lasioglossum, the most species rich genus captured in our study, where half of the species captured (10 spp.)were specific to one type of landscape. As indicated by our data, loss of heterogeneous landscapes (such as different successional states across a largely forested landscapes) may extirpate those species that require unique habitats, thus reducing wild bee diversity and community resilience to environmental change. The implementation of wildflower plantings, hedgerows and increasing seminatural habitats within homogeneous landscapes provides a way to generate the heterogeneous environment that may offer the refuge for those bees that are landscape specific (Steffan-Dewenter et al. 2002; Williams and Kremen 2007; Le Féon et al. 2010; Kremen and M’Gonigle 2015; Decocq et al. 2016). Due to the regional nature of this study, future research is needed in order to replicate and compare our findings across New England and beyond.

Conclusions

It is critical to understand how habitat requirements influence wild bee distribution within landscapes so that decisions regarding conservation will have the most positive impact. We found that overall wild bee abundance and richness in forested landscapes exhibiting multiple states of different forest successional stages were influenced by the amount of canopy cover present.Our results are consistent with the findings of other studies in forested environments which indicate the negative relationship between wild bee abundance and diversity and canopy cover (Grundel et al. 2010; Roberts et al. 2017; Breland et al. 2018; Odanaka et al. 2020).Successional states that maintained higher bee abundance and richness had less canopy and abundant bare ground. Our data further indicates that wild bee conservation practices and current means of forest management could be complimentary. Both aim to reduce tree density in forested areas, while opening the canopy and raising understory temperatures, which benefit both wild bee communities and understory plants (Taki et al.2013, 2007; Hudson et al. 2013; Hanula et al. 2015). Reduction of tree density, through managed burns or manual thinning, exposes more ground, allowing for usage by ground nesting bees (Hanula et al. 2015, 2016). Our data suggests that maintaining heterogenous landscapes through supporting multiple successional states aids in promoting wild bee diversity especially in areas that are prone to lacking diversity, such as agriculturally dominant areas.

Supplementary information

Supplementary information accompanies this paper at https://doi.org/10.1186/s40663-020-00241-4.

Acknowledgements

We thank Jacob Withee, Wyatt Shell, Molly Jacobson, Stephanie Gardner,Erika Tucker, and Minna Mathiasson (University of New Hampshire) for their help with fieldwork, specimen processing, identifications and databasing.

Authors’contributions

KAO analyzed data and drafted manuscript; SMR conceived study, assisted with data analyses and edited manuscript. The authors read and approved the final manuscript.

Funding

USDA National Institute of Food and Agriculture Hatch Project 1004515 and Foundation for Food and Agriculture Research Pollinator Health fund 549038.

Availability of data and materials

All specimens are housed in the Rehan lab at York University, data and specimens will be made available upon request.

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Received: 8 January 2020 Accepted: 7 April 2020