Using X-ray Microscopy and Hg L3 XANES To Study Hg Binding in the Rhizosphere of Spartina Cordgrass

详细信息    查看全文

• 作者：Cynthia Patty ; Brandy Barnett ; Bridget Mooney ; Amanda Kahn ; Silvio Levy ; Yijin Liu ; Piero Pianetta ; Joy C. Andrews
• 刊名：Environmental Science & Technology
• 出版年：2009
• 出版时间：October 1, 2009
• 年：2009
• 卷：43
• 期：19
• 页码：7397-7402
• 全文大小：189K
• 年卷期：v.43,no.19(October 1, 2009)
• ISSN：1520-5851

文摘

San Francisco Bay has been contaminated historically by mercury from mine tailings as well as contemporary industrial sources. Native Spartina foliosa and non-native S. alterniflora-hybrid cordgrasses are dominant florae within the SF Bay estuary environment. Understanding mercury uptake and transformations in these plants will help to characterize the significance of their roles in mercury biogeochemical cycling in the estuarine environment. Methylated mercury can be biomagnified up the food web, resulting in levels in sport fish up to 1 million times greater than in surrounding waters and resulting in advisories to limit fish intake. Understanding the uptake and methylation of mercury in the plant rhizosphere can yield insight into ways to manage mercury contamination. The transmission X-ray microscope on beamline 6-2 at the Stanford Synchrotron Radiation Lightsource (SSRL) was used to obtain absorption contrast images and 3D tomography of Spartina foliosa roots that were exposed to 1 ppm Hg (as HgCl₂) hydroponically for 1 week. Absorption contrast images of micrometer-sized roots from S. foliosa revealed dark particles, and dark channels within the root, due to Hg absorption. 3D tomography showed that the particles are on the root surface, and slices from the tomographic reconstruction revealed that the particles are hollow, consistent with microorganisms with a thin layer of Hg on the surface. Hg L₃ XANES of ground-up plant roots and Hg L₃ micro-XANES from microprobe analysis of micrometer-sized roots (60−120 μm in size) revealed three main types of speciation in both Spartina species: Hg−S ligation in a form similar to Hg(II) cysteine, Hg−S bonding as in cinnabar and metacinnabar, and methylmercury-carboxyl bonding in a form similar to methylmercury acetate. These results are interpreted within the context of obtaining a “snapshot” of mercury methylation in progress.