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Paleolimnology and Resurrection Ecology: The Future of Reconstructing the Past

Overview
Journal Evol Appl
Specialty Biology
Date 2018 Jan 6
PMID 29302271
Citations 9
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Abstract

Paleolimnologists have utilized lake sediment records to understand historical lake and landscape development, timing and magnitude of environmental change at lake, watershed, regional and global scales, and as historical datasets to target watershed and lake management. Resurrection ecologists have long recognized lake sediments as sources of viable propagules ("seed or egg banks") with which to explore questions of community ecology, ecological response, and evolutionary ecology. Most researchers consider as the primary model organism in these efforts, but many other aquatic biota, from viruses to macrophytes, similarly produce viable propagules that are incorporated in the sediment record but have been underutilized in resurrection ecology. The common goals shared by these two disciplines have led to mutualistic and synergistic collaborations-a development that must be encouraged to expand. We give an overview of the achievements of paleolimnology and the reconstruction of environmental history of lakes, review the untapped diversity of aquatic organisms that produce dormant propagules, compare as a model of resurrection ecology with other organisms amenable to resurrection studies, especially diatoms, and consider new research directions that represent the nexus of these two fields.

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References
1.
Dyhrman S, Jenkins B, Rynearson T, Saito M, Mercier M, Alexander H . The transcriptome and proteome of the diatom Thalassiosira pseudonana reveal a diverse phosphorus stress response. PLoS One. 2012; 7(3):e33768. PMC: 3315573. DOI: 10.1371/journal.pone.0033768. View

2.
Becks L, Ellner S, Jones L, Hairston Jr N . The functional genomics of an eco-evolutionary feedback loop: linking gene expression, trait evolution, and community dynamics. Ecol Lett. 2012; 15(5):492-501. DOI: 10.1111/j.1461-0248.2012.01763.x. View

3.
Lefebvre K, Hamilton P, Pick F . A comparison of molecular markers and morphology for Neidium taxa (Bacillariophyta) from eastern North America. J Phycol. 2017; 53(3):680-702. DOI: 10.1111/jpy.12537. View

4.
Lack J, Weider L, Jeyasingh P . Whole genome amplification and sequencing of a Daphnia resting egg. Mol Ecol Resour. 2017; 18(1):118-127. DOI: 10.1111/1755-0998.12720. View

5.
Weis A . Detecting the "invisible fraction" bias in resurrection experiments. Evol Appl. 2018; 11(1):88-95. PMC: 5748523. DOI: 10.1111/eva.12533. View