Particle size distribution and optimal capture of aqueous macrobial eDNA
Version of Record online: 16 JUN 2014
© 2014 The Authors. Methods in Ecology and Evolution published by John Wiley & Sons Ltd on behalf of British Ecological Society
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Methods in Ecology and Evolution
Volume 5, Issue 7, pages 676–684, July 2014
How to Cite
Turner, C. R., Barnes, M. A., Xu, C. C. Y., Jones, S. E., Jerde, C. L., Lodge, D. M. (2014), Particle size distribution and optimal capture of aqueous macrobial eDNA. Methods in Ecology and Evolution, 5: 676–684. doi: 10.1111/2041-210X.12206
- Issue online: 15 JUL 2014
- Version of Record online: 16 JUN 2014
- Accepted manuscript online: 16 MAY 2014 03:42AM EST
- Manuscript Accepted: 2 MAY 2014
- Manuscript Received: 17 DEC 2013
- Illinois-Indiana Sea Grant. Grant Number: NA10OAR4170068
- Great Lakes Restoration Initiative. Grant Number: FY10-S-T0240-O169-2
- NSF IGERT. Grant Number: 0504495
Fig. S1. Histograms of qPCR-measured Carp eDNA copies per reaction. Note that the axis scales differ between histograms.
Fig. S2. Micrographs of the pore structure of commonly available filter materials illustrating that only polycarbonate (A) and nylon net (B) filters have uniformly size pores
Appendix S1. Extended methodological details
Table S1. Published methods for capturing aqueous eDNA from macrofauna.
Table S2. Pond concentrations of Carp eDNA, total eDNA and SPM in each size fraction.
Table S3. Lake concentrations of Carp eDNA, total eDNA and SPM in each size fraction.
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