Abstract:We studied flight distance and directionality of bee pollinators on the tropical shrub weed Triumfetta semitriloba Jacq. (Tiliaceae), addressing (1) within-and between-plant movement pattern; (2) distances flown between plants; (3) flight directionality. Flowering plants were distributed in well-delimited clumps, in each of two pasture areas (A1 and A2) and one area of forest gap (A3), in Viçosa, southeastern Brazil. Five solitary bee species, Augochlorella michaelis, Augochloropsis cupreola, Pseudocentron pau… Show more
“…This is consistent with a previous study of this fig (Moore et al, 2003b). Similar 'nearest neighbour' approaches to floral visitation have also been seen in unrelated pollinating insects including five solitary bee and two social bee species (Collevatti et al, 2000). (Ramirez, 1970;Janzen, 1979).…”
Section: Discussionsupporting
confidence: 91%
“…Our results showed that after re-emerging, K. tentacularis foundresses (that are then wingless) could re-enter and oviposit in up to four further receptive figs and that they tended to enter the first receptive figs they encountered. Similar 'nearest neighbour' approaches to floral visitation have also been seen in unrelated pollinating insects including five solitary bee and two social bee species (Collevatti et al, 2000). Similar 'nearest neighbour' approaches to floral visitation have also been seen in unrelated pollinating insects including five solitary bee and two social bee species (Collevatti et al, 2000).…”
The interaction between figs (Ficus spp., Moraceae) and their pollinator fig wasps (Hymenoptera: Agaonidae) is an obligate mutualism, but females of dioecious fig trees exploit fig wasps without providing rewards. Figs are closed inflorescences that typically trap pollinator females after entry, but some fig wasp species can re-emerge (although wingless) and subsequently oviposit in and pollinate further figs. Using glasshouse populations, we examined the sex ratios and clutches laid by single foundresses of Kradibia tentacularis (Grandi) in their first and subsequent male figs of Ficus montana Blume, and how the probability of emergence and entering a second fig varied between seasons. A maximum of four figs were entered by any one foundress. Wingless foundresses were able to locate and enter figs up to 60 cm from the first fig they entered, but the probability of entry declined sharply with distance from that fig. The foundresses that re-emerged produced slightly higher adult offspring totals than those that failed to re-emerge. Clutch sizes of a single foundress in its first fig equalled those in all the subsequent figs combined, with clutch size per fig decreasing when more figs were entered. Smaller clutches had less female-biased sex ratios. Figs were more numerous in summer than in winter, but the proportion of figs entered by only wingless foundresses remained unchanged.Movement between figs increases pollinator reproductive success in male figs, thereby encouraging foundresses that encounter a female tree to also move between and pollinate several female figs.
“…This is consistent with a previous study of this fig (Moore et al, 2003b). Similar 'nearest neighbour' approaches to floral visitation have also been seen in unrelated pollinating insects including five solitary bee and two social bee species (Collevatti et al, 2000). (Ramirez, 1970;Janzen, 1979).…”
Section: Discussionsupporting
confidence: 91%
“…Our results showed that after re-emerging, K. tentacularis foundresses (that are then wingless) could re-enter and oviposit in up to four further receptive figs and that they tended to enter the first receptive figs they encountered. Similar 'nearest neighbour' approaches to floral visitation have also been seen in unrelated pollinating insects including five solitary bee and two social bee species (Collevatti et al, 2000). Similar 'nearest neighbour' approaches to floral visitation have also been seen in unrelated pollinating insects including five solitary bee and two social bee species (Collevatti et al, 2000).…”
The interaction between figs (Ficus spp., Moraceae) and their pollinator fig wasps (Hymenoptera: Agaonidae) is an obligate mutualism, but females of dioecious fig trees exploit fig wasps without providing rewards. Figs are closed inflorescences that typically trap pollinator females after entry, but some fig wasp species can re-emerge (although wingless) and subsequently oviposit in and pollinate further figs. Using glasshouse populations, we examined the sex ratios and clutches laid by single foundresses of Kradibia tentacularis (Grandi) in their first and subsequent male figs of Ficus montana Blume, and how the probability of emergence and entering a second fig varied between seasons. A maximum of four figs were entered by any one foundress. Wingless foundresses were able to locate and enter figs up to 60 cm from the first fig they entered, but the probability of entry declined sharply with distance from that fig. The foundresses that re-emerged produced slightly higher adult offspring totals than those that failed to re-emerge. Clutch sizes of a single foundress in its first fig equalled those in all the subsequent figs combined, with clutch size per fig decreasing when more figs were entered. Smaller clutches had less female-biased sex ratios. Figs were more numerous in summer than in winter, but the proportion of figs entered by only wingless foundresses remained unchanged.Movement between figs increases pollinator reproductive success in male figs, thereby encouraging foundresses that encounter a female tree to also move between and pollinate several female figs.
“…Os principais visitantes florais de Eugenia uniflora, E. neonitida, E. punicifolia e E. rotundifolia, que são abelhas de pequeno porte e moscas, apresentam uma amplitude forrageira baixa, comportamento que pode vir a diminuir o fluxo gênico entre as populações vegetais, diferentemente do que acontece com grandes polinizadores, como abelhas de grande porte, pássaros e mamíferos que podem carregar o pólen por longas distâncias (Collevatti et al 2000;Latouche-Hallé et al 2004).…”
RESUMO -(Biologia floral e da polinização de quatro espécies de Eugenia L. (Myrtaceae)). Eugenia uniflora, E. punicifolia, E. neonitida e E. rotundifolia são espécies perenes, geralmente de porte arbustivo, que ocorrem na restinga do Parque Natural Municipal de Grumari, região oeste do Município do Rio de Janeiro. Possuem inflorescências racemosas com flores pediceladas inseridas nas axilas foliares. Suas flores são andróginas, polistêmones, do tipo Papaver, generalistas, com grãos de pólen como único recurso floral sendo enquadradas dentro da categoria de "flores-pólen". O estigma é seco, diminuto e formado por papilas delgadas. A antese é diurna, as flores duram apenas um dia e são visitadas por uma ampla variedade de insetos, incluindo himenópteros, dípteros, coleópteros e neurópteros, totalizando 29 espécies. As abelhas são os visitantes mais comuns e, dentre elas, Apis mellifera L., espécie introduzida pela ação humana, é a mais freqüente e abundante, sendo considerada o polinizador efetivo das espécies aqui estudadas. A floração é anual e em massa.
“…Such pattern of variation could, in principle, favour generalization to all phenotypes by pollinators and prevent populations from maintaining their differences owing to increased gene flow. However, insect pollinators only perceive colours at relatively small spatial distances (Giurfa et al 1996;Dyer et al 2008) and move mostly between neighbouring plants (Waser 1982;Collevatti et al 2000;Saleh and Chittka 2007), which implies that they perceive colour variation only at a very local scale. Therefore, there may be discontinuous transitions at spatial scales that are biologically meaningful for pollinators even if flower colour variation seems continuous when considering all the plants of the hybrid zone together.…”
To assess if pollinators' behaviour could explain the maintenance of hybrid zones between different flower colour morphs, we analyzed flower colour variation in an Antirrhinum hybrid zone using spectrometry and a model of bee perception. Some colours generated by hybridization were not observed in any Antirrhinum species and even appeared to be rare among angiosperms. Variation in flower colours within the hybrid zone was continuous; the most similar colours were predicted not to be discriminated from one another in natural foraging situations. However, when compared at a scale corresponding to bees' foraging range, some flower colours could be discriminated from all colours displayed by neighbouring plants. This could affect pollinator behaviour and explain lower visitation rates within the centre of the hybrid zone. Behavioural studies involving bumblebees and plant mixtures of parental and hybrid flower colours carefully characterized with appropriate visual models will be necessary to test this hypothesis.
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