Cited by 16Seed Germination and PhysiologySeedling growth and survival studiesEcology and Vegetation Dynamics Studies

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Rainfall seasonality predicts the germination behavior of a tropical dry‐forest vine

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Abstract

Seed dormancy is considered to be an adaptive strategy in seasonal and/or unpredictable environments because it prevents germination during climatically favorable periods that are too short for seedling establishment. Tropical dry forests are seasonal environments where seed dormancy may play an important role in plant resilience and resistance to changing precipitation patterns. We studied the germination behavior of seeds from six populations of the Neotropical vine Dalechampia scandens (Euphorbiaceae) originating from environments of contrasting rainfall seasonality. Seeds produced by second greenhouse‐generation plants were measured and exposed to a favorable wet environment at different time intervals after capsule dehiscence and seed dispersal. We recorded the success and the timing of germination. All populations produced at least some dormant seeds, but seeds of populations originating from more seasonal environments required longer periods of after‐ripening before germinating. Within populations, larger seeds tended to require longer after‐ripening periods than did smaller seeds. These results indicate among‐population genetic differences in germination behavior and suggest that these populations are adapted to local environmental conditions. They also suggest that seed size may influence germination timing within populations. Ongoing changes in seasonality patterns in tropical dry forests may impose strong selection on these traits.

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Figure 1 Map of Dalechampia scandens study populations, with colors indicating precipitation seasonality (CV of monthly precipitation in %). CC: Ciudad del Carmen; LM: La Mancha; PM: Puerto Morelos; S23: Rincón de la Vieja; T: Tulum
Figure 1 Map of Dalechampia scandens study populations, with colors indicating precipitation seasonality (CV of monthly precipitation in %). CC: Ciudad del Carmen; LM: La Mancha; PM: Puerto Morelos; S23: Rincón de la Vieja; T: TulumCC BY · PubMed Central
Figure 2 Pseudanthial blossom of Dalechampia scandens (Euphorbiaceae), a common vine occurring throughout the lowland Neotropics, from Mexico to Argentina. To assess the relationship between historical environmental conditions and seed dormancy, we studied the germination behavior of seeds from populations of this species originating from regions characterized by different degrees of seasonality. The photographed blossom is in the bisexual phase: visible are three receptive stigmas (borne on three pistillate flowers), one open male flower, and the resin gland (bearing white resin). (Photo by P.H. Olsen)
Figure 2 Pseudanthial blossom of Dalechampia scandens (Euphorbiaceae), a common vine occurring throughout the lowland Neotropics, from Mexico to Argentina. To assess the relationship between historical environmental conditions and seed dormancy, we studied the germination behavior of seeds from populations of this species originating from regions characterized by different degrees of seasonality. The photographed blossom is in the bisexual phase: visible are three receptive stigmas (borne on three pistillate flowers), one open male flower, and the resin gland (bearing white resin). (Photo by P.H. Olsen)CC BY · PubMed Central
Figure 3 Estimated proportion of seeds germinating as a function of after‐ripening time, that is, the time from seed dispersal to watering. Solid lines are from the first experiment, and dashed lines are from the second experiment. Lines are extrapolated beyond the experimental periods to illustrate the full shape of the response curves (see Supporting Information Figures S2 and S3 for lines fitted to the data from each experiment)
Figure 3 Estimated proportion of seeds germinating as a function of after‐ripening time, that is, the time from seed dispersal to watering. Solid lines are from the first experiment, and dashed lines are from the second experiment. Lines are extrapolated beyond the experimental periods to illustrate the full shape of the response curves (see Supporting Information Figures S2 and S3 for lines fitted to the data from each experiment)CC BY · PubMed Central
Figure 4 Effects of seed size on T 50, the number of days of after‐ripening necessary to yield 50% germination, in the first (top row) and second (lower row) experiments. The solid lines are given by T 50 = −(α + xβseed)/βtime and are drawn over the range of seed sizes (x) in each population, as indicated by the histograms above each panel
Figure 4 Effects of seed size on T 50, the number of days of after‐ripening necessary to yield 50% germination, in the first (top row) and second (lower row) experiments. The solid lines are given by T 50 = −(α + xβseed)/βtime and are drawn over the range of seed sizes (x) in each population, as indicated by the histograms above each panelCC BY · PubMed Central
Figure 5 Among‐population relationship between mean T 50, the number of days of after‐ripening necessary to yield 50% germination, and seed size (measured as seed mass in mg). Error bars indicate standard errors
Figure 5 Among‐population relationship between mean T 50, the number of days of after‐ripening necessary to yield 50% germination, and seed size (measured as seed mass in mg). Error bars indicate standard errorsCC BY · PubMed Central
Figure 6 Among‐population relationship between mean T 50, the number of days of after‐ripening necessary to yield 50% germination, and precipitation seasonality. Error bars indicate standard errors
Figure 6 Among‐population relationship between mean T 50, the number of days of after‐ripening necessary to yield 50% germination, and precipitation seasonality. Error bars indicate standard errorsCC BY · PubMed Central

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Metadata

Authors
Martins, A. A., Opedal, Ø. H., Armbruster, W. S., & Pélabon, C.
Affiliations
  • Norwegian University of Science and Technology (NO)
  • University of Helsinki (FI)
  • University of Alaska Fairbanks (US)
Corresponding author
Martins, Adriana A.
Venue
Ecology and Evolution
Publisher
Wiley
Published
2019-04-04
Volume
9
Issue
9
Pages
5196-5205
ISSN
2045-7758 (ISSN-L)
OpenAlex
W2921774583
Cited by
16
References
0
Citations by year
2026: 2 · 2025: 5 · 2024: 1 · 2023: 1 · 2022: 4 · 2021: 2 · 2019: 1
FWCI
1.29
Type
journal article
Language
en
Open access
Locations
  • Ecology and Evolution (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Työväentutkimus Vuosikirja (submittedVersion)
  • Lund University Publications (Lund University) (submittedVersion)
Funders
Norges Forskningsråd (223257)
Topics
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Seed Germination and Physiology
  • Life Sciences › Agricultural and Biological Sciences › Forestry › Seedling growth and survival studies
  • Physical Sciences › Environmental Science › Nature and Landscape Conservation › Ecology and Vegetation Dynamics Studies
Keywords
seed dormancy, germination timing, precipitation seasonality, Dalechampia scandens, tropical dry forest, after-ripening, seed size, Euphorbiaceae, vines, rainfall variability, local adaptation

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CoChat. (2026). Citation check: Rainfall seasonality predicts the germination behavior of a tropical dry‐forest vine. https://app.cochat.ai/papers/10.1002/ece3.5108
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Martins, A. A., Opedal, Ø. H., Armbruster, W. S., & Pélabon, C. (2019). Rainfall seasonality predicts the germination behavior of a tropical dry‐forest vine. Ecology and Evolution. https://doi.org/10.1002/ece3.5108