1. Climate-change effects on plants and pollinators
Climate change constitutes a vast, uncontrolled experiment with the world’s ecosystems. Warming is changing the timing (phenology) of flowering and insect activity, reducing snowpack in high-altitude and high-latitude regions, and intensifying summer droughts. We still don’t know much about the consequences of these changes for plant and pollinator populations.
In the past, I have studied the possibility that climate change might disrupt temporal synchrony between plants and pollinating insects (Forrest & Thomson 2010, Am. J. Bot.; Forrest & Thomson 2011, Ecol. Monogr.; see also my 2015 Oikos Forum/review piece on this topic). Former MSc student Gabriel Gauthier used our lab’s long(ish)-term observations of solitary bee populations to evaluate the extent to which variation in synchrony matters for bee reproduction (manuscript in preparation). My lab has also been investigating the consequences of warmer summers (see Forrest & Chisholm 2017, Ecology) for bee survival and fitness. This work is funded primarily by NSERC, with help from RMBL.
Cavity-nesting solitary bees (mainly in the family Megachilidae) are my preferred study system for this work. They are important pollinators of wildflowers and certain crops, and—conveniently—they are willing to nest in artificial structures (“trap-nests“) that allow standardization, monitoring, and experimental manipulation. Trap-nests consist of holes drilled in wood and lined with translucent, removable straws that let a researcher monitor nesting progress. To learn how to build a trap-nest, visit the USDA Bee Lab’s How to Build a Nesting Block site.
2. Bees on farms
Despite the growing climate crisis, land-use change (specifically, conversion of natural habitat to agriculture) so far remains the #1 cause of biodiversity loss globally. There is a certain dark irony in this, because much of our food production depends, directly or indirectly, on biodiversity—including a diverse range of wild pollinators.
My lab has begun to investigate the bee communities of agricultural ecosystems (agro-ecosystems) in the Ottawa–Montreal area—how they are affected by landscape features such as flower availability through time (former MSc student Jessica Guezen) and presence of nesting habitat (PhD student Cécile Antoine; see also Forrest et al. 2015, J. Appl. Ecol.), and also how these wild bee communities affect crop yield (former PhD student Gail MacInnis). This work is funded by an Ontario ERA.
3. Life-history strategies of solitary bees
Several solitary bee species display what appears to be a bet-hedging life-history strategy, with cohort emergence split among two or more years—a trait that should confer resilience to environmental variation. We are interested in better understanding the distribution (geographic, ecological, phylogenetic) and adaptive value of such life-history traits, with the goal of better predicting which taxa and habitats will be most vulnerable to future environmental change.
I have also become increasingly interested in the evolutionary causes and ecological consequences of pollen specialization in solitary bees (see work of former MSc student Megan McAulay). This work is funded by NSERC.
4. Functional significance of floral traits
For many plants, sex depends on getting animal pollinators to visit flowers and move pollen from anthers to stigmas. We are interested in the various traits plants have evolved to achieve these ends. For example, we have investigated the adaptive significance of style length and floral orientation in Mertensia (Forrest et al. 2011, Ann. Bot.; Lin & Forrest in press, J. Plant Ecol.) and of pollen colour (yellow to dark red) in Erythronium (Austen et al. 2018, Ecology).
Artificial “flowers”, which can be designed to isolate the effects of particular floral variables, are useful tools for understanding the functional roles of floral traits. For example, we have used artificial flowers in a controlled flight-cage setting with captive bees to study the effect of background complexity on colour preference of bumble bees (Forrest & Thomson 2009, Naturwissenschaften; Rivest et al. 2017, Evol. Ecol.) and the potential for floral symmetry to affect the consistency of pollinator entry angles (Culbert & Forrest 2016, J. Poll. Ecol.).
5. Parasites of solitary bees
Cavity-nesting bees are attacked by a variety of brood parasites (or kleptoparasites), of which the most abundant at our Colorado field sites are sapygid wasps (pictured below, middle). These wasps inflict substantial mortality on bee populations, but not all bees are equally susceptible to parasite attack (see Spear et al. 2016, Am. Nat.). My students and I are studying the factors influencing parasitism rates in cavity-nesting bees (see Forrest & Chisholm 2017, Ecology; Groulx & Forrest 2018, Ecol. Entomol.) and investigating how selection imposed by brood parasites interacts with selection imposed by floral resources and the abiotic environment.
6. Selection and constraint in the evolution of flowering phenology
In the past, I have used simulation modelling to look at how reproductive phenology responds to different kinds of selection. For example, certain aspects of bumble bee foraging behaviour (specifically, positive frequency-dependence and avoidance of unfamiliar flowers) can select against early flowering in a plant population (Forrest & Thomson 2009, Proc. R. Soc. B). On the other hand, sexual selection can favour early-flowering individuals (Forrest 2014, Am. Nat.). Recently, colleagues and I (led by post-doc Dr. Emily Austen) published our thoughts on why natural selection so often appears to favour early-flowering plants (Austen et al. 2017, New Phyt.).