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Sökning: WFRF:(Borges Renee M)

  • Resultat 1-4 av 4
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1.
  • Junker, Robert R., et al. (författare)
  • Covariation and phenotypic integration in chemical communication displays : Biosynthetic constraints and eco-evolutionary implications
  • 2018
  • Ingår i: New Phytologist. - : Wiley. - 0028-646X .- 1469-8137. ; 220:3, s. 739-749
  • Tidskriftsartikel (refereegranskat)abstract
    • Chemical communication is ubiquitous. The identification of conserved structural elements in visual and acoustic communication is well established, but comparable information on chemical communication displays (CCDs) is lacking. We assessed the phenotypic integration of CCDs in a meta-analysis to characterize patterns of covariation in CCDs and identified functional or biosynthetically constrained modules. Poorly integrated plant CCDs (i.e. low covariation between scent compounds) support the notion that plants often utilize one or few key compounds to repel antagonists or to attract pollinators and enemies of herbivores. Animal CCDs (mostly insect pheromones) were usually more integrated than those of plants (i.e. stronger covariation), suggesting that animals communicate via fixed proportions among compounds. Both plant and animal CCDs were composed of modules, which are groups of strongly covarying compounds. Biosynthetic similarity of compounds revealed biosynthetic constraints in the covariation patterns of plant CCDs. We provide a novel perspective on chemical communication and a basis for future investigations on structural properties of CCDs. This will facilitate identifying modules and biosynthetic constraints that may affect the outcome of selection and thus provide a predictive framework for evolutionary trajectories of CCDs in plants and animals.
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2.
  • Somanathan, Hema, et al. (författare)
  • Nocturnal Bees Feed on Diurnal Leftovers and Pay the Price of Day – Night Lifestyle Transition
  • 2020
  • Ingår i: Frontiers in Ecology and Evolution. - : Frontiers Media SA. - 2296-701X. ; 8
  • Tidskriftsartikel (refereegranskat)abstract
    • Bees exemplify flights under bright sunlight. A few species across bee families have evolved nocturnality, displaying remarkable adaptations to overcome limitations of their daylight-suited apposition eyes. Phase inversion to nocturnality in a minority of bees that co-exist with diurnal bees provides a unique opportunity to study ecological benefits that mediate total temporal niche shifts. While floral traits and sensory modalities associated with the evolution of classical nocturnal pollination syndromes, e.g. by bats and moths, are well-studied, nocturnality in bees represents a poorly understood, recently invaded, extreme niche. To test the competitive release hypothesis, we examine how nocturnality shapes foraging by comparing pollen loads, nest pollen, and flower visitation of sympatric nocturnal and diurnal carpenter bees. We predicted that nocturnal bees primarily use night-blooming flowers, show little/no resource overlap with diurnal species and competitive release favors night-time pollen collection for provisioning. Contrarily, we found substantial resource overlap between nocturnal and diurnal bees. Flower opening times, floral longevity and plant abundance did not define nocturnal flower use. Smaller pollen loads on nocturnal foragers suggest subsistence on resource leftovers largely from diurnal flowers. Greater pollen types/diversity on nocturnal foragers indicate lower floral constancy compared to diurnal congenerics. Reduced activity during new moon compared to full moon suggests constraints to nocturnal foraging. Invasion and sustenance within the nocturnal niche is characterized by: (i) opportunistic foraging on residual resources as indicated by smaller pollen loads, extensive utilization of day-blooming flowers and substantial overlap with diurnal bees, (ii) generalization at two levels—between and within foraging trips as indicated by lower floral constancy, (iii) reduced foraging on darker nights, indicating visual constraints despite sensitive optics. This together with smaller populations and univoltine breeding in nocturnal compared to multivoltine diurnal counterparts suggest that nocturnality imposes substantial fitness costs. In conclusion, the evolution of nocturnality in bees is accompanied by resource generalization instead of specialization. Reduced floral constancy suggests differences in foraging strategies of nocturnal and diurnal bees which merits further investigation. The relative roles of competition, floral rewards and predators should be examined to fully understand the evolution and maintenance of nocturnality in bees.
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3.
  • Borges, Renee M., et al. (författare)
  • Patterns and processes in nocturnal and crepuscular pollination services
  • 2016
  • Ingår i: Quarterly Review of Biology. - : University of Chicago Press. - 0033-5770 .- 1539-7718. ; 91:4, s. 389-418
  • Tidskriftsartikel (refereegranskat)abstract
    • Night,dawn,and dusk have abiotic features that differ from the day. Illumination,wind speeds,turbulence,and temperatures are lower while humidity may be higher at night. Nocturnal pollination occurred in 30% of angiosperm families across 68% of orders,97% of families with C3,two-thirds of fam-ilies with crassulacean acid metabolism (CAM),and 71% dicot families with C4 photosynthesis. Despite its widespread occurence,nocturnal pollination occurs in more families with xerophytic adaptations than helophytes or mesophytes,suggesting that nocturnal flowering is primarily an adaptation to water stress since flowering is a water-intensive process. We propose the arid or water stress hypothesis for nocturnal flowering suggesting that plants facing water stress in a habitat (e.g.,deserts) or a habitat stratum (e.g.,upper canopy for epiphytes) gain a selective advantage by nocturnal flowering by reducing water loss through evapotranspiration,leading to larger flowers that provide more nectar or other resources,to support pollinators with higher rewards. Contrary to the wide taxonomic occurrence of nocturnal flowering,few animal taxa serve as nocturnal pollinators. We discuss the sensory and physiological abilities that enable pollinator movement,navigation,and detection of flowers within the nocturnal temporal niche and present a unified framework for investigation of nocturnal flowering and pollination.
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4.
  • Somanathan, Hema, et al. (författare)
  • Resolution and sensitivity of the eyes of the Asian honeybees Apis florea, Apis cerana and Apis dorsata.
  • 2009
  • Ingår i: Journal of Experimental Biology. - : The Company of Biologists. - 1477-9145 .- 0022-0949. ; 212:Pt 15, s. 2448-2453
  • Tidskriftsartikel (refereegranskat)abstract
    • Bees of the genus Apis are important foragers of nectar and pollen resources. Although the European honeybee, Apis mellifera, has been well studied with respect to its sensory abilities, learning behaviour and role as pollinators, much less is known about the other Apis species. We studied the anatomical spatial resolution and absolute sensitivity of the eyes of three sympatric species of Asian honeybees, Apis cerana, Apis florea and Apis dorsata and compared them with the eyes of A. mellifera. Of these four species, the giant honeybee A. dorsata (which forages during moonlit nights) has the lowest spatial resolution and the most sensitive eyes, followed by A. mellifera, A. cerana and the dwarf honeybee, A. florea (which has the smallest acceptance angles and the least sensitive eyes). Moreover, unlike the strictly diurnal A. cerana and A. florea, A. dorsata possess large ocelli, a feature that it shares with all dim-light bees. However, the eyes of the facultatively nocturnal A. dorsata are much less sensitive than those of known obligately nocturnal bees such as Megalopta genalis in Panama and Xylocopa tranquebarica in India. The differences in sensitivity between the eyes of A. dorsata and other strictly diurnal Apis species cannot alone explain why the former is able to fly, orient and forage at half-moon light levels. We assume that additional neuronal adaptations, as has been proposed for A. mellifera, M. genalis and X. tranquebarica, might exist in A. dorsata.
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