Urbanization is a major anthropogenic driver of decline for ecologically and economically important taxa including bees. Despite their generally negative impact on pollinators, cities can display a surprising degree of biodiversity compared to other landscapes. The pollinating communities found within these environments, however, tend to be filtered by interacting local and landscape features that comprise the urban matrix. Landscape and local features exert variable influence on pollinators within and across taxa, which ultimately affects community composition in such a way that contributes to functional trait homogenization and reduced phylogenetic diversity. Although previous results are not easily generalizable, bees and pollinators displaying functional trait characteristics such as polylectic diet, cavity-nesting behavior, and later emergence appear most abundant across different examined cities. To preserve particularly vulnerable species, most notably specialists that have become underrepresented within city communities, green spaces like parks and urban gardens have been examined as potential refuges. Such spaces are scattered across the urban matrix and vary in pollinator resource availability. Therefore, ensuring such spaces are optimized for pollinators is imperative. This review examines how urban features affect pollinators in addition to ways these green spaces can be manipulated to promote greater pollinator abundance and diversity.

To evaluate sociality in small carpenter bees (CeratinaLatreille), we studied the life history and nesting biology of a common eastern North American species,Ceratina(Zadontomerus)calcarataRobertson. Pan-trap and nest collections throughout the active season (May to September 2006) were used to assessC. calcarata’sseasonal phenology and nesting biology in southern Ontario. Adults overwintered in their natal nests. Males emerged in early May and occupied preexisting hollows in twigs and stems. Females emerged from hibernacula 2 weeks later, founding new nests. Nest founding and provisioning occurred throughout the spring; females remained with developing brood through the summer. Complete nests contained, on average, 6.9 offspring, with egg-to-adult development averaging 46 days.Ceratina calcaratais subsocial rather than solitary: mothers are long-lived and nest-loyal, and care for offspring from egg to adulthood. Subsociality is found in all behaviourally classified small carpenter bees, while some species cross the boundary into social life, makingCeratinaan important genus for the study of the transition between solitary and social life.

The evolution of eusociality is a perennial issue in evolutionary biology, and genomic advances have fueled steadily growing interest in the genetic changes underlying social evolution. Along with a recent flurry of research on comparative and evolutionary genomics in different eusocial insect groups (bees, ants, wasps, and termites), several mechanistic explanations have emerged to describe the molecular evolution of eusociality from solitary behavior. These include solitary physiological ground plans, genetic toolkits of deeply conserved genes, evolutionary changes in protein-coding genes, cis regulation, and the structure of gene networks, epigenetics, and novel genes. Despite this proliferation of ideas, there has been little synthesis, even though these ideas are not mutually exclusive and may in fact be complementary. We review available data on molecular evolution of insect sociality and highlight key biotic and abiotic factors influencing social insect genomes. We then suggest both phylogenetic and ecological evolutionary developmental biology (eco-evo-devo) perspectives for a more synthetic view of molecular evolution in insect societies.

The origin of sterile worker castes, resulting in eusociality, represents one of the major evolutionary transitions in the history of life. Understanding how eusociality has evolved is therefore an important issue for understanding life on earth. Here we show that in the large bee subfamily Xylocopinae, a simple form of sociality was present in the ancestral lineage and there have been at least four reversions to purely solitary nesting. The ancestral form of sociality did not involve morphological worker castes and maximum colony sizes were very small. True worker castes, entailing a life-time commitment to non-reproductive roles, have evolved only twice, and only one of these resulted in discrete queen-worker morphologies. Our results indicate extremely high barriers to the evolution of eusociality. Its origins are likely to have required very unusual life-history and ecological circumstances, rather than the amount of time that selection can operate on more simple forms of sociality.