<?xml version="1.0" encoding="UTF-8"?><rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcq="http://purl.org/dc/terms/"><records count="1" morepages="false" start="1" end="1"><record rownumber="1"><dc:product_type>Dataset</dc:product_type><dc:title>Data from: Bet hedging is not sufficient to explain germination patterns of a winter annual plant</dc:title><dc:creator>Geber, Monica; Moeller, David; Eckhart, Vincent; Siegmund, Gregor-Fausto</dc:creator><dc:corporate_author/><dc:editor/><dc:description>Bet hedging consists of life history strategies that buffer against
 environmental variability by trading off immediate and long-term fitness.
 Delayed germination in annual plants is a classic example of bet hedging
 and is often invoked to explain low germination fractions. We examined
 whether bet hedging explains low and variable germination fractions among
 20 populations of the winter annual plant Clarkia xantiana ssp. xantiana
 that experience substantial variation in reproductive success among years.
 Leveraging 15 years of demographic monitoring and 3 years of field
 germination experiments, we assessed the fitness consequences of seed
 banks and compared optimal germination fractions from a
 density-independent bet-hedging model to observed germination fractions.
 We did not find consistent evidence of bet hedging or the expected
 trade-off between arithmetic and geometric mean fitness, though delayed
 germination increased long-term fitness in 7 of 20 populations. Optimal
 germination fractions were 2 to 5 times higher than observed germination
 fractions, and among-population variation in germination fractions was not
 correlated with risks across the life cycle. Our comprehensive test
 suggests that bet hedging is insufficient to explain the observed
 germination patterns. Understanding variation in germination strategies
 will likely require integrating bet hedging with complementary forces
 shaping the evolution of delayed germination.</dc:description><dc:publisher>Dryad</dc:publisher><dc:date>2022-01-01</dc:date><dc:nsf_par_id>10554495</dc:nsf_par_id><dc:journal_name/><dc:journal_volume/><dc:journal_issue/><dc:page_range_or_elocation/><dc:issn/><dc:isbn/><dc:doi>https://doi.org/10.5061/dryad.np5hqbzx4</dc:doi><dcq:identifierAwardId>1754299</dcq:identifierAwardId><dc:subject>FOS: Biological sciences</dc:subject><dc:subject>FOS: Biological sciences</dc:subject><dc:subject>Life History Evolution</dc:subject><dc:subject>bet hedging</dc:subject><dc:subject>seed banks</dc:subject><dc:subject>delayed germination</dc:subject><dc:subject>Clarkia xantiana ssp. xantiana</dc:subject><dc:subject>demographic data</dc:subject><dc:subject>plant population dynamics</dc:subject><dc:size>1866539 bytes</dc:size><dc:version_number/><dc:location>California</dc:location><dc:rights>Creative Commons Zero v1.0 Universal</dc:rights><dc:institution/><dc:sponsoring_org>National Science Foundation</dc:sponsoring_org></record></records></rdf:RDF>