Douglas Sponsler

Dr. Douglas Sponsler


Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 July 2023 in Ecography
Verified
Journal Article
Open access
DSDouglas Sponsler
Douglas Sponsler
AIAaron Iverson
Aaron Iverson
ISIngolf Steffan‐Dewenter
Ingolf Steffan‐Dewenter
The mutualism between plants and pollinators is built upon the trophic ecology of flowers and florivores. Yet the ecology of flowers‐as‐food is left implicit in most studies of plant–pollinator ecology, and it has been largely neglected in mainstream trophic ecology. This deficit is especially evident in an emerging issue of basic and applied significance: competition between pollinators for floral resources. In this synthesis, we start by exploring the notion of floral resource limitation upon which most studies concerning competition between pollinators are tacitly predicated. Both theoretical and empirical lines of evidence indicate that floral resource limitation must be understood as a complex ecological contingency; the question is not simply whether but when, where and in what regions of floral trait space resources are limiting. Based on this premise, we propose a framework for understanding floral resource availability in terms of temporal, spatial and functional structure. While this framework is conceptually intuitive, it is empirically and analytically demanding. We review existing methods for measuring and summarizing the multi‐dimensional structure of floral resources, highlight their strengths and weaknesses, and identify opportunities for future methods development. We then discuss the causal relationships linking floral resource structure to species coexistence, plant–pollinator community dynamics, and exogenous drivers like climate, land use, and episodic disturbances. In its role as both cause and effect, floral resource structure mediates the relationship between behavioral ecology, landscape ecology, and coexistence theory with respect to flowers and florivores. Establishing floral resource structure as an object of study and application will both shed light on basic questions of coexistence and guide management decisions concerning contentious issues such as the compatibility of apiculture with wild pollinator conservation and the appropriate use of floral enhancements in agri‐environment schemes.

27 April 2020 in Ecosphere
Verified
Journal Article
Open access
PDF file
DSDouglas Sponsler
Douglas Sponsler
DSDon Shump
Don Shump
RRRodney T. Richardson
Rodney T. Richardson
CGChristina M. Grozinger
Christina M. Grozinger
Roughly a third of described insect species visit flowers, making the flower–insect interface one of the chief pillars of global biodiversity. Studying flower–insect relationships at the scale of communities and landscapes has been hindered, however, by the methodological challenges of quantifying landscape‐scale floral resources. This challenge is especially acute in urban landscapes, where traditional floral surveying techniques are ill‐suited to the unique constraints of built environments. To surmount these challenges, we devised a “honey bee foraging assay” approach to floral resource surveying, wherein continuous colony weight tracking and DNA metabarcoding of pollen samples are used to capture both the overall availability and taxonomic composition of floral resources. We deploy this methodology in the complex urban ecosystem of Philadelphia, Pennsylvania, USA. Our results reveal distinct seasonality of floral resource availability, with pulses of high availability in May, June, and September, and a period of prolonged scarcity in August. Pollen genus richness mirrored this pattern, with peak richness in May and June. The taxonomic composition of pollen samples varied seasonally, reflecting underlying floral phenology, with especially strong turnover between May and June samples and between August and September samples delineating well‐defined spring, summer, and fall floral resource communities. Trait analysis also revealed seasonal structure, with spring samples characterized by trees and shrubs, summer samples including a stronger presence of herbaceous “weeds”, and fall samples dominated by woody vines. Native flora predominated in spring, giving way to a preponderance of exotic flora in summer and fall. At a basic level, this yields insight into the assembly of novel urban floral resource communities, showcasing, for example, the emergence of a woody vine‐dominated fall flora. At an applied level, our data can inform urban land management, such as the design of ecologically functional ornamental plantings, while also providing practical guidance to beekeepers seeking to adapt their management activities to floral resource seasonality. Methodologically, our study demonstrates the potential of the honey bee foraging assay as a powerful technique for landscape‐scale floral resource surveying, provided the inherent biases of honey bee foraging are accounted for in the interpretation of the results.

2 April 2021 in People and Nature
Verified
Journal Article
Open access
PDF file
DSDouglas Sponsler
Douglas Sponsler
EBEve Z. Bratman
Eve Z. Bratman
The term ‘urban beekeeping’ connotes a host of meanings—sociopolitical, commercial, ecological and personal—beyond the mere description of where bees and beekeepers happen to coincide. Yet, these meanings are seldom articulated explicitly or brought into critical engagement with the relevant fields of urban ecology and political ecology. Beginning with a brief account of the history of urban beekeeping in the United States, we draw upon urban ecological theory to construct a conceptual model of urban beekeeping that distinguishes beekeepingin,ofandforthe city. In our model, beekeepinginthe city describes the mere importation of the traditionally rural practice of beekeeping into urban spaces for the private reasons of the individual beekeeper, whereas beekeepingofthe city describes beekeeping that is consciously tailored to the urban context, often accompanied by (semi)professionalization of beekeepers and the formation of local expert communities (i.e. beekeeping associations). Beekeepingforthe city describes a shift in mindset in which beekeeping is directed to civic ends beyond the boundaries of the beekeeping community per se. Using this framework, we identify and discuss specific socioecological assets and liabilities of urban beekeeping, and how these relate to beekeepingin,ofandforthe city. We then formulate actionable guidelines for maturing the practice of urban beekeeping into a beneficent and self‐critical form of urban ecological citizenship; these include fostering self‐regulation within the beekeeping community, harnessing beekeeping as a ‘gateway’ experience for a broader rapprochement between urban residents and nature, and recognizing the political‐ecological context of beekeeping with respect to matters of socioecological justice. A freePlain Language Summarycan be found within the Supporting Information of this article.

27 April 2022 in Ecology
Verified
Journal Article
Open access
DSDouglas Sponsler
Douglas Sponsler
FRFabrice Requier
Fabrice Requier
KKKatharina Kallnik
Katharina Kallnik
ACAlice Classen
Alice Classen
FMFabienne Maihoff
Fabienne Maihoff
ISIngolf Steffan‐Dewenter
Ingolf Steffan‐Dewenter
Environmental gradients generate and maintain biodiversity on Earth. Mountain slopes are among the most pronounced terrestrial environmental gradients, and the elevational structure of species and their interactions can provide unique insight into the processes that govern community assembly and function in mountain ecosystems. We recorded bumble bee–flower interactions over 3 years along a 1400‐m elevational gradient in the German Alps. Using nonlinear modeling techniques, we analyzed elevational patterns at the levels of abundance, species richness, species β‐diversity, and interaction β‐diversity. Though floral richness exhibited a midelevation peak, bumble bee richness increased with elevation before leveling off at the highest sites, demonstrating the exceptional adaptation of these bees to cold temperatures and short growing seasons. In terms of abundance, though, bumble bees exhibited divergent species‐level responses to elevation, with a clear separation between species preferring low versus high elevations. Overall interaction β‐diversity was mainly caused by strong turnover in the floral community, which exhibited a well‐defined threshold of β‐diversity rate at the tree line ecotone. Interaction β‐diversity increased sharply at the upper extreme of the elevation gradient (1800–2000 m), an interval over which we also saw steep decline in floral richness and abundance. Turnover of bumble bees along the elevation gradient was modest, with the highest rate of β‐diversity occurring over the interval from low‐ to mid‐elevation sites. The contrast between the relative robustness bumble bee communities and sensitivity of plant communities to the elevational gradient in our study suggests that the strongest effects of climate change on mountain bumble bees may be indirect effects mediated by the responses of their floral hosts, though bumble bee species that specialize in high‐elevation habitats may also experience significant direct effects of warming.

20 December 2021 in Oikos
Verified
Journal Article
Open access
PDF file
DSDouglas Sponsler
Douglas Sponsler
KKKatharina Kallnik
Katharina Kallnik
FRFabrice Requier
Fabrice Requier
ACAlice Classen
Alice Classen
AMA. Fabienne Maihoff
A. Fabienne Maihoff
ISIngolf Steffan‐Dewenter
Ingolf Steffan‐Dewenter
Patterns of resource use by animals can clarify how ecological communities have assembled in the past, how they currently function and how they are likely to respond to future perturbations. Bumble bees (Hymentoptera: Bombus spp.) and their floral hosts provide a diverse yet tractable system in which to explore resource selection in the context of plant–pollinator networks. Under conditions of resource limitation, the ability of bumble bees species to coexist should depend on dietary niche overlap. In this study, we report patterns and dynamics of floral morphotype preferences in a mountain bumble bee community based on ~13 000 observations of bumble bee floral visits recorded along a 1400 m elevation gradient. We found that bumble bees are highly selective generalists, rarely visiting floral morphotypes at the rates predicted by their relative abundances. Preferences also differed markedly across bumble bee species, and these differences were well‐explained by variation in bumble bee tongue length, generating patterns of preference similarity that should be expected to predict competition under conditions of resource limitation. Within species, though, morphotype preferences varied by elevation and season, possibly representing adaptive flexibility in response to the high elevational and seasonal turnover of mountain floral communities. Patterns of resource partitioning among bumble bee communities may determine which species can coexist under the altered distributions of bumble bees and their floral hosts caused by climate and land use change.

10 January 2024 in Proceedings Of The Royal Society B-Biological Sciences
Verified
Journal Article
Open access
FBFabian A. Boetzl
Fabian A. Boetzl
DSDouglas Sponsler
Douglas Sponsler
MAMatthias Albrecht
Matthias Albrecht
PBPéter Batáry
Péter Batáry
KBKlaus Birkhofer
Klaus Birkhofer
JSJens Schirmel
Jens Schirmel
Natural pest and weed regulation are essential for agricultural production, but the spatial distribution of natural enemies within crop fields and its drivers are mostly unknown. Using 28 datasets comprising 1204 study sites across eight Western and Central European countries, we performed a quantitative synthesis of carabid richness, activity densities and functional traits in relation to field edges (i.e. distance functions). We show that distance functions of carabids strongly depend on carabid functional traits, crop type and, to a lesser extent, adjacent non-crop habitats. Richness of both carnivores and granivores, and activity densities of small and granivorous species decreased towards field interiors, whereas the densities of large species increased. We found strong distance decays in maize and vegetables whereas richness and densities remained more stable in cereals, oilseed crops and legumes. We conclude that carabid assemblages in agricultural landscapes are driven by the complex interplay of crop types, adjacent non-crop habitats and further landscape parameters with great potential for targeted agroecological management. In particular, our synthesis indicates that a higher edge–interior ratio can counter the distance decay of carabid richness per field and thus likely benefits natural pest and weed regulation, hence contributing to agricultural sustainability.