MASTING BY EIGHTEEN NEW ZEALAND PLANT SPECIES: THE ROLE OF TEMPERATURE AS A SYNCHRONIZING CUE

By Eric, Schauber, Dave Kelly, P. Turchin, C. Simon, William, Lee, Robert, Allen, Ian and 7 more. 2002

318 citations recorded by the source corpus.

Subfields: Ecology, Ecology, Evolution, Behavior and Systematics, Genetics

View Paper: https://www.semanticscholar.org/paper/ae9acb6546feaa85c148fb5d1db8a463c957f983

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Citations in the corpus

The Ecology of Seeds: References (2005, background): “In New Zealand, persistent seeds are significantly smaller than transient seeds (Moles et al., 2000), although the relationship is driven entirely by the absence of transient seed banks among species with very small ( 0.5 mg) seeds.”
Large‐scale pest control in New Zealand beech forests (2016, background): “Predicting and measuring beech seedfall A relationship between beech seedfall and previous summer temperatures has been known since at least 1948 (Poole 1948), and this idea was examined quantitatively by Allen and Platt (1990), Schauber et al. (2002), Kelly et al. (2013), Allen et al. (2014).”
Masting and trophic cascades: interplay between rowan trees, apple fruit moth, and their parasitoid in southern Norway (2004, background): “…have confirmed the impact of climatic fluctuations (such as temperature and precipitation level) correlated across large scale on spatial synchrony in seed production even in the absence of pollen limitation (Koenig and Knops 1998, 2000, Koenig et al. 1999, Rees et al. 2002, Schauber et al. 2002).”
Local‐scale synchrony and variability in mast seed production patterns of Picea glauca (2007, background): “Also, abnormally high temperatures in the summer before seedfall, consistent with the La Niña phase of the El Niño Southern Oscillation, has been associated with synchronous fruiting in multiple species across New Zealand (Schauber et al. 2002).”
Cues versus proximate drivers: testing the mechanism behind masting behavior (2014, methodology): “All statistics were calculated in R 2.10.1 using the package nlme (Pinheiro et al. 2009).”
MAST SEEDING IN PERENNIAL PLANTS: Why, How, Where? (2002, background): “…570 studies of≥6 years duration compiled from reviews (Silvertown 1980, Webb & Kelly 1993, Kelly 1994, Herrera et al. 1998, Kelly et al. 2000, Koenig 438 KELLY ¥ SORK & Knops 2000, Schauber et al. 2002) and the primary literature (Appendix A, http://www.annualreviews.org/MastingAppendix.html).”
CLIMATE AND NET CARBON AVAILABILITY DETERMINE TEMPORAL PATTERNS OF SEED PRODUCTION BY NOTHOFAGUS (2005, background): “Decadal-level warming (e.g., Salinger 1995) could increase mean seed production in instances where seed production is related to a temperature cue (e.g., Schauber et al. 2002).”
Spatial Synchrony in Population Dynamics (2004, background): “Numerical tracking of prey populations by predator populations can lead to synchrony, as illustrated by interspecific synchrony between mast-seeding plants and their seed predators (Curran & Webb 2000, Schauber et al. 2002, Satake et al. 2004).”
EXPLOITING TEMPORAL VARIABILITY TO UNDERSTAND TREE RECRUITMENT RESPONSE TO CLIMATE CHANGE (2007, unknown): “Interannual variation has long been used to analyze climate regulation of tree growth (Graumlich 1991, Clark et al. 2003a, Stevens et al. 2006) and fecundity (McKone et al. 1998, Schauber et al. 2002, Hampe 2005, Mutke et al. 2005).”
Climate cues and resources interact to determine seed production by a masting species (2011, background): “This synchronization of reproductive effort by plant species can occur over great distances (Herrera et al. 1998; Kelly & Sork 2002; Schauber et al. 2002; Selås et al. 2002; Mduma, Sinclair & Turkington 2007).”
Declines in common, widespread native birds in a mature temperate forest. (2010, background): “, 2002), and there has been an increase in the frequency of major seedfall events in this region over the period of our study (Schauber et al., 2002; Wilson et al., 1998).”
How does climate warming affect plant-pollinator interactions? (2009, background): “Mass flowering, i.e. masting, is also generally positively affected by high temperatures (Schauber et al. 2002).”
Testing the resource-matching hypothesis in the mast seeding tree Nothofagus truncata (Fagaceae) (2006, methodology): “It is thought that flowering in Nothofagus is triggered by warm dry summers during the previous year (Wardle 1984; Allen & Platt 1990; Schauber et al. 2002) with Nothofagus populations showing considerable within- and between-species synchrony over spatial scales in excess of several hundred…”
What defines mast seeding? Spatio‐temporal patterns of cone production by whitebark pine (2011, background): “…is the best metric of mast seeding in cases where ecologists want to pick up more subtle differences in masting among populations or species, such as differential responses to changing climate (McKone, Kelly & Lee 1998; Schauber et al. 2002) or species interactions (Schnurr, Ostfeld & Canham 2002).”
Factors influencing survival and long-term population viability of New Zealand long-tailed bats (Chalinolobus tuberculatus): Implications for conservation (2005, background): “High levels of beech seedfall and increased over-winter survival of rodents are both increased by warmer than average temperatures (Schauber et al., 2002).”
Have the Harmful Effects of Introduced Rats on Islands been Exaggerated? (2006, background): “Beech (Nothofagus spp.) forests of the South Island of New Zealand periodically produce massive crops of seed in a phenomenon known as masting (Schauber et al. 2002).”