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. 2009 Oct 29;4(10):e7653.
doi: 10.1371/journal.pone.0007653.

Phenotypic plasticity of leaf shape along a temperature gradient in Acer rubrum

Affiliations

Phenotypic plasticity of leaf shape along a temperature gradient in Acer rubrum

Dana L Royer et al. PLoS One. .

Abstract

Both phenotypic plasticity and genetic determination can be important for understanding how plants respond to environmental change. However, little is known about the plastic response of leaf teeth and leaf dissection to temperature. This gap is critical because these leaf traits are commonly used to reconstruct paleoclimate from fossils, and such studies tacitly assume that traits measured from fossils reflect the environment at the time of their deposition, even during periods of rapid climate change. We measured leaf size and shape in Acer rubrum derived from four seed sources with a broad temperature range and grown for two years in two gardens with contrasting climates (Rhode Island and Florida). Leaves in the Rhode Island garden have more teeth and are more highly dissected than leaves in Florida from the same seed source. Plasticity in these variables accounts for at least 6-19% of the total variance, while genetic differences among ecotypes probably account for at most 69-87%. This study highlights the role of phenotypic plasticity in leaf-climate relationships. We suggest that variables related to tooth count and leaf dissection in A. rubrum can respond quickly to climate change, which increases confidence in paleoclimate methods that use these variables.

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Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. Map of seed collection sites (circles) and common gardens (large squares).
ON = Burlington, Ontario; PA = Erie, Pennsylvania; RI = University of Rhode Island; SC = Savannah River, South Carolina; FL = Tall Timbers Research Station, Florida. Maps generated using GMT software (http://www.aquarius.ifm-geomar.de; Lambert azimuthal equal-area projection). Bar = 100 km.
Figure 2
Figure 2. Representative leaves of Acer rubrum used in study.
Leaf derived from Ontario seed stock grown in (A) Rhode Island and (B) Florida; leaf derived from Florida seed stock grown in (C) Rhode Island and (D) Florida. For all leaves, petioles have been removed and minor damage along the margin has been corrected with white lines. Bar (for all leaves) = 1 cm.
Figure 3
Figure 3. Leaf size and shape of Acer rubrum.
Plants come from four different seed stocks and were grown in two gardens with contrasting climates. Variables are clustered into three groups: (A–C) leaf dissection; (D–F) tooth number, and (G–K) leaf and tooth size. ON, Ontario; PA, Pennsylvania; SC, South Carolina; FL, Florida; RI, Rhode Island; peri, perimeter. See Table 1, Figs. 1, and Materials and Methods for details about seed collection sites and gardens. Differences between gardens reflect phenotypic plasticity, while differences among seed stock probably mostly reflect genetic differences among ecotypes. Standard errors are plotted.
Figure 4
Figure 4. Sensitivity of number of teeth/leaf perimeter to mean annual temperature in Acer rubrum.
RI = Rhode Island; FL = Florida. See Fig. 1 and Materials and Methods for details about gardens. Differences within a single seed source reflects plasticity within a genotype; differences within a single garden, and within the Royer et al. data set, probably mostly reflect genetic differences among ecotypes. Garden data are identical to Fig. 3E.

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