2010
DOI: 10.1086/654846
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Pollination of Philodendron acutatum (Araceae) in the Atlantic Forest of Northeastern Brazil: A Single Scarab Beetle Species Guarantees High Fruit Set

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Cited by 58 publications
(51 citation statements)
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References 38 publications
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“…Indeed, this evolutionary scenario may be widespread, and explain the pertinent, although not ubiquitous, evolution of pollination syndromes in floral signaling. However, it may be premature to exclude the possibility of (micro) coevolution in highly specialized, mutualistic pollination systems, such as those that have evolved in some Dynastine scarabs and arum lilies (Gottsberger and Silberbauer‐Gottsberger 1991; Maia and Schlindwein 2006; Maia et al 2010). In such close relationships, the floral scents of plants and the olfactory preferences of scarabs may have coevolved, allowing highly specific communication between the plants and their pollinators (Maia 2011).…”
Section: Discussionmentioning
confidence: 99%
“…Indeed, this evolutionary scenario may be widespread, and explain the pertinent, although not ubiquitous, evolution of pollination syndromes in floral signaling. However, it may be premature to exclude the possibility of (micro) coevolution in highly specialized, mutualistic pollination systems, such as those that have evolved in some Dynastine scarabs and arum lilies (Gottsberger and Silberbauer‐Gottsberger 1991; Maia and Schlindwein 2006; Maia et al 2010). In such close relationships, the floral scents of plants and the olfactory preferences of scarabs may have coevolved, allowing highly specific communication between the plants and their pollinators (Maia 2011).…”
Section: Discussionmentioning
confidence: 99%
“…Floral food rewards for these scarab beetles are diverse and include sterile staminate or staminode tissue (Prance 1976, 1980, Young 1986, Maia et al 2010, Maldonado et al 2015), carpellary appendages (Prance and Arias 1975, Hirthe and Porembski 2003), stamens (Dieringer and Espinosa 1994, Hirthe and Porembski 2003, Costa et al 2017), petal tissue (Gibbs et al 1977, Gottsberger 1989, Dieringer and Espinosa 1994, Dieringer et al 1999, Voeks 1992), specialized adaxial food tissue of bracts (Beach 1982), and pollen (Rickson et al 1990). Cyclocephala amazona was observed consuming epidermal trichomes from the stalk of Bactris gasipaes Kunth (Arecaceae) inflorescences before feeding on pollen (Rickson et al 1990).…”
Section: Cyclocephalines As Floral Visitorsmentioning
confidence: 99%
“…Detailed studies on Dieffenbachia Schott (Araceae) indicate that among a group of cyclocephaline floral visitors, some species are relatively more effective pollinators (Young 1988a). Seasonal abundance of cyclocephalines at a specific locality, along with floral phenology, may also determine which species are primary or secondary pollinators (Maia et al 2010, Costa et al 2017). …”
Section: Cyclocephalines As Floral Visitorsmentioning
confidence: 99%
“…This also actively released resin in Philodendron is not a floral reward nor is it involved in the attraction of pollinators, which are cyclocephaline beetles of the family Scarabaeidae (Gottsberger & Amaral 1984;Gottsberger 1986;Gibernau et al 1999;Gibernau & Barabé 2002;Gottsberger & SilberbauerGottsberger 2006;Maia et al 2010;Gottsberger et al 2013). However, it makes part of the fine-tuned pollination mechanism.…”
Section: Introductionmentioning
confidence: 99%