TY - JOUR
T1 - Cuticle and subsurface ornamentation of intact plant leaf epidermis under confocal and superresolution microscopy
AU - Urban, Michael A.
AU - Barclay, Richard S.
AU - Sivaguru, Mayandi
AU - Punyasena, Surangi W.
N1 - Funding Information:
RSB acknowledges funding from the Smithsonian's National Museum of Natural History (Peter Buck Deep Time Fellowship and the Paleobotany Fund). Support for MAU, MS, and SWP provided by the US National Science Foundation Advances in Biological Informatics (NSF DBI-1262561 to SWP). Scott Wing and Kirk Johnson of NMNH provided fossil samples. Rusty Russell and Debbie Bell of the US National Herbarium provided permission to sample herbarium specimens. Steven Siegler also provided permission to sample herbarium specimens at the University of Illinois Herbarium. NMNH volunteer Pam Hamilton imaged Ginkgo biloba specimens under eSEM at the NMNH Imaging Laboratory, run by Scott Whittaker. We thank the editor of MRT and the reviewers for their comments, which helped improve the manuscript.
Publisher Copyright:
© 2016 Wiley Periodicals, Inc.
PY - 2018/2/1
Y1 - 2018/2/1
N2 - Plant cuticle micromorphology is an invaluable tool in modern ecology and paleoecology. It has expanded our knowledge of systematic relationships among diverse plant groups and can be used to identify fossil plants. Furthermore, fossil plant leaf micromorphology is used for reconstructing past environments, most notably for estimating atmospheric CO2 concentration. Here we outline a new protocol for imaging plant cuticle for archival and paleoecological applications. Traditionally, both modern reference and fossil samples undergo maceration with subsequent imaging via environmental SEM, widefield fluorescence, or light microscopy. In this paper, we demonstrate the capabilities of alternative preparation and imaging methods using confocal and superresolution microscopy with intact leaf samples. This method produces detailed three-dimensional images of surficial and subsurface structures of the intact leaf. Multiple layers are captured simultaneously, which previously required independent maceration and microtome steps. We compared clearing agents (chloral hydrate, KOH, and Visikol); mounting media (Eukitt and Hoyer's); fluorescent stains (periodic acid Schiff, propidium iodide); and confocal vs. superresolution microscopes. We conclude that Eukitt is the best medium for long-term preservation and imaging. Because of nontoxicity and ease of procurement, Visikol made for the best clearing agent. Staining improves contrast and under most circumstances PAS provided the clearest images. Supperresolution produced higher clarity images than traditional confocal, but the information gained was minimal. This new protocol provides the botanical and paleobotanical community an alternative to traditional techniques. Our proposed workflow has the net benefit of being more efficient than traditional methods, which only capture the surface of the plant epidermis. Microsc. Res. Tech. 81:129–140, 2018.
AB - Plant cuticle micromorphology is an invaluable tool in modern ecology and paleoecology. It has expanded our knowledge of systematic relationships among diverse plant groups and can be used to identify fossil plants. Furthermore, fossil plant leaf micromorphology is used for reconstructing past environments, most notably for estimating atmospheric CO2 concentration. Here we outline a new protocol for imaging plant cuticle for archival and paleoecological applications. Traditionally, both modern reference and fossil samples undergo maceration with subsequent imaging via environmental SEM, widefield fluorescence, or light microscopy. In this paper, we demonstrate the capabilities of alternative preparation and imaging methods using confocal and superresolution microscopy with intact leaf samples. This method produces detailed three-dimensional images of surficial and subsurface structures of the intact leaf. Multiple layers are captured simultaneously, which previously required independent maceration and microtome steps. We compared clearing agents (chloral hydrate, KOH, and Visikol); mounting media (Eukitt and Hoyer's); fluorescent stains (periodic acid Schiff, propidium iodide); and confocal vs. superresolution microscopes. We conclude that Eukitt is the best medium for long-term preservation and imaging. Because of nontoxicity and ease of procurement, Visikol made for the best clearing agent. Staining improves contrast and under most circumstances PAS provided the clearest images. Supperresolution produced higher clarity images than traditional confocal, but the information gained was minimal. This new protocol provides the botanical and paleobotanical community an alternative to traditional techniques. Our proposed workflow has the net benefit of being more efficient than traditional methods, which only capture the surface of the plant epidermis. Microsc. Res. Tech. 81:129–140, 2018.
KW - Zeiss LSM 880 Airyscan
KW - confocal
KW - leaf epidermis
KW - micromorphology
KW - stomata
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U2 - 10.1002/jemt.22667
DO - 10.1002/jemt.22667
M3 - Article
C2 - 27111826
AN - SCOPUS:85040974933
SN - 1059-910X
VL - 81
SP - 129
EP - 140
JO - Microscopy research and technique
JF - Microscopy research and technique
IS - 2
ER -