Floral longevity and attraction of Arctic Lupine, Lupinus Arcticus: Implications for pollination efficiency In this study, I found that floral longevity of Lupinus arct...
Floral morphology differs among new northern highbush blueberry cultivars Variation in floral morphology and timing of bloom are commo...
Gradual replacement of wild bees by honeybees in flowers of the Mediterranean basin over the last 50 years Evidence for pollinator declines largely originates from mid...
The temporal build-up of hummingbird/plant mutualisms in north America and temperate south America The 361 species of hummingbirds that occur from Alaska to Pa...
Abundance drives broad patterns of generalisation in plant–humming bird pollination networks Abundant pollinators are often more generalised than rare po...
Artificial pollination and fruit quality in red Pitaya A native of the Americas, pitaya is currently a fruit-bearin...
Berry unexpected: Nocturnal pollination of lowbush blueberry Lowbush blueberry (syn. ‘‘wild blueberry’’), Vaccini...
Effects of a possible pollinator crisis on food crop production in Brazil Animal pollinators contribute to human food production and s...
Interspecific pollinator movements reduce pollen deposition and seed production in Mimulus Ringens The movement of pollinators between co-flowering plant speci...
Systematic definition of threatened fauna communities is critical to their conservation Most terrestrial ecological communities are defined primaril...
Per-visit pollinator performance and regional importance of wild Bombus and Andrena (Melandrena) compared to the managed honey bee in New York apple orchards Declines in honey bee health and increasing demand for polli...
Pollination systems, biogeography, and divergence times of three allopatric species of Schisandra in north America, China, and Japan This study analyses the pollination systems and biogeography...