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Identification of major quantitative trait loci underlying floral pollination syndrome divergence in Penstemon

Distinct floral pollination syndromes have emerged multiple ...

Indirect effects of landscape spatial structure and plant species richness on pollinator diversity in Ozark glades

Changes in landscape spatial structure—specifically, reduc...

Pollination in the oil palms Elaeis guineensis, E. Oleifera and their hybrids in tropical America

Oil palm (Elaeis guineensis) is very important in the Centra...

Pollinator scarcity drives the shift to delayed selﬁng in Himalayan mayapple Podophyllum Hexandrum

Recent molecular phylogenetics has indicated that American m...

The evolution of Cayaponia. Repeated shifts from bat to bee pollination and long-distance dispersal to Africa 2 – 5 million years ago

Unlabelled: Premise of the study: The Cucurbitaceae genus Ca...

The influence of climatic seasonality on the diversity of different tropical pollinator groups

Tropical South America is rich in different groups of pollin...

The science policy field tour concept: A new platform for communicating science for public policy

The public is concerned about reports of decreasing pollinat...

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...

Why are queens broodless- failed nest initiation not linked to parasites, mating status, or ovary development in two bumble bee species of Pyrobombus

Bumble bees (Bombus [Hymenoptera: Apidae]) are important po...

Effects of a possible pollinator crisis on food crop production in Brazil

Animal pollinators contribute to human food production and s...

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...

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