EVALUATING THE WIND POLLINATION BENEFITS OF MAST SEEDING

By D. Kelly, D. Hart, R. Allen. 2001

216 citations recorded by the source corpus.

Subfields: Ecology, Ecology, Evolution, Behavior and Systematics, Insect Science

View Paper: https://www.semanticscholar.org/paper/7e097f7aa986c7f093b24a87df3b20295e5d5299

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Ecology

1. OTTAR N. Bjørnstad
2. S. Boutin
3. J. LaMontagne
4. S. B. Wall
5. V. Sork
6. A. Monks
7. A. Satake
8. D. Kelly

In Ecology, Evolution, Behavior and Systematics

1. OTTAR N. Bjørnstad
2. S. Boutin
3. J. LaMontagne
4. S. B. Wall
5. V. Sork
6. A. Monks
7. A. Satake
8. D. Kelly

In Insect Science

1. S. B. Wall
2. S. Boutin
3. J. LaMontagne
4. K. Thompson
5. D. Kelly
6. OTTAR N. Bjørnstad
7. V. Sork

Citations in the corpus

• LONG-TERM PATTERNS OF ACORN PRODUCTION FOR FIVE OAK SPECIES IN XERIC FLORIDA UPLANDS (2003, unknown): “…as the evolved responses of predator satiation, enhancement of wind-pollination success, animal pollination and dispersal enhancement, and environmental prediction, as reviewed by Kelly (1994), Koenig et al. (1994), Yamauchi (1996), Kelly et al. (2001), Kelly and Sork (2003, andVander Wall (2002).”
• Evolutionary advantages of mast seeding in Fagus crenata (2005, background): “In other species benefits range from relatively small (Chionochloa pallens), via moderate (Dacrydium cupressinum, Betula alleghaniensis) to large (Nothofagus solandri and N. menziesii) (Kelly et al. 2001).”
• MASTING BY EIGHTEEN NEW ZEALAND PLANT SPECIES: THE ROLE OF TEMPERATURE AS A SYNCHRONIZING CUE (2002, background): “Nothofagus spp. may benefit from masting primarily through improved pollination success (Wardle 1984, Burrows and Allen 1991, Kelly et al. 2001) rather than predator satiation.”
• MAST SEEDING IN PERENNIAL PLANTS: Why, How, Where? (2002, background): “The species most likely to gain benefits are those whose pollination success at the long-term average flowering effort is low compared to the maximum achievable with superabundant pollen (Kelly et al. 2001).”
• Masting and trophic cascades: interplay between rowan trees, apple fruit moth, and their parasitoid in southern Norway (2004, background): “…survivorship of seedlings by satiating seed predators (the ‘‘predator satiation hypothesis’’, Janzen 1971, Silvertown 1980, Nilsson and Wästljung 1987) or, for wind pollinated trees, how masting improves pollination efficiency (Nilsson and Wästljung 1987, Smith et al. 1990, Kelly et al. 2001).”
• The Ecology of Seeds: References (2005, background): “Wind-pollination efficiency can be increased greatly by the economies of scale brought about by episodic mass flowering, at least in some cases (Smith et al., 1990; Kelly et al., 2001).”
• Climatic factors controlling reproduction and growth of Norway spruce in southern Norway (2002, background): “Masting behaviour may be explained by different nonmutually exclusive hypotheses, between which predator satiation and wind pollination are up to now believed to have a prior role (e.g., Herrera et al. 1998; Kelly et al. 2001).”
• Testing the resource-matching hypothesis in the mast seeding tree Nothofagus truncata (Fagaceae) (2006, background): “Recent work on Nothofagus solandri and N. menziesii has shown quantitatively that both species gain very large pollination benefits from masting, by increasing the percentage of seeds which are viable from <10% in low-seed years to >60% in mast years (Kelly et al. 2001).”
• Synchrony and asynchrony: observations and hypotheses for the flowering wave in a long‐lived semelparous bamboo (2004, background): “In mast-fruiting, iteroparous plants and especially those that are wind-pollinated as most bamboo appear to be (e.g. Nadgauda et al., 1993; John et al., 1995), synchrony may also be advantageous in improving outcross pollination rates (Kelly et al., 2001; Koenig & Ashley, 2003).”
• Local‐scale synchrony and variability in mast seed production patterns of Picea glauca (2007, background): “However, mobile generalist seed predators may show the opposite of predator satiation (i.e. higher proportion of the seed crop consumed in high seed years or for high-seed trees), as shown for Betula allegheniensis (Kelly et al. 2001).”
• How plants manipulate the scatter-hoarding behaviour of seed-dispersing animals (2010, background): “For the pollination hypothesis, synchronized flower production in wind-pollinated plants is credited with increasing seed set (Smith et al. 1990; Kelly et al. 2001).”