2017
DOI: 10.1111/jse.12240
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Pollen limitation, plasticity in floral traits, and mixed mating system in an alpine plant Pedicularis siphonantha (Orobanchaceae) from different altitudes

Abstract: Plant mating systems rapidly respond to pollen limitation in changing environments. However, whether and how floral traits are involved in a mating system shift requires further investigation. A widely distributed and bumblebee‐pollinated lousewort, Pedicularis siphonantha D. Don was studied. We investigated pollination systems, reproductive success, and floral traits in four large populations growing from 3200 m to 4300 m. Pollinator activity in low altitude populations was lower and these populations had a d… Show more

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Cited by 11 publications
(7 citation statements)
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“…It seems that as elevation increases, pollen limitation may be more severe, because in the alpine zone above the treeline, flower visitation rates declined with increasing elevation (Arroyo et al, 1982, 1985; Bingham & Orthner, 1998). In four large populations of Pedicularis siphonantha (Orobanchaceae) from 3200 to 4300 m, pollinator activity, fruit set and seed number were lower in high‐altitude populations (Dai et al, 2017b).…”
Section: Pollen Limitationmentioning
confidence: 99%
“…It seems that as elevation increases, pollen limitation may be more severe, because in the alpine zone above the treeline, flower visitation rates declined with increasing elevation (Arroyo et al, 1982, 1985; Bingham & Orthner, 1998). In four large populations of Pedicularis siphonantha (Orobanchaceae) from 3200 to 4300 m, pollinator activity, fruit set and seed number were lower in high‐altitude populations (Dai et al, 2017b).…”
Section: Pollen Limitationmentioning
confidence: 99%
“…In general, floral traits are found to be less variable and less affected by environmental heterogeneity than vegetative traits because variation in floral morphology may have negative effects on fitness (Berg 1960 ; Frazee and Marquis 1994 ). Nevertheless, population variation has been detected in stigma–anther separation (Griffin and Willi, 2014 ; Papuga et al 2015 ), floral display (Dai et al 2017 ; Lambrecht et al 2017 ), and pollen–ovule ratio (Guo et al 2010 ; Dai et al 2017 ). This variation in floral traits is usually related to variation in the pollination environment (Aigner 2004 ) and some studies have detected increased pollen limitation at the distributional edges (Moeller et al 2012 ), although others do not record any increase in pollen limitation, presumably due to increase in resource constraints or self-pollination (Totland 2001 ; Hargreaves et al 2015 ).…”
Section: Introductionmentioning
confidence: 99%
“…The number of ovules is a more conservative floral trait than pollen production in the evolution of flowering plants’ breeding systems [ 51 ]. This was proven in a series of taxa [ 10 , 52 , 53 ]. In this study, the number of pollen grains per flower differed in space and time, while the ovules per flower remained unchanged.…”
Section: Discussionmentioning
confidence: 94%
“…tibetica (Bonati) Tsoong has a very short raceme in which all flowers open on the same plane; an appropriate corolla-tube length is essential for a flower to display on the plane. For P. siphonantha , the long raceme allows the flowers with varied corolla-tube lengths to open at different positions on the inflorescence [ 52 ].…”
Section: Discussionmentioning
confidence: 99%
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