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This material explores the complexities of light stable isotope abundances and the variability in quality assurance and control across different labs, emphasizing that not all facilities provide the same level of data integrity. Key factors affecting carbon isotope values include moisture stress, salinity, light levels, canopy height, and lifespan of plants. It also highlights technological advances such as Tunable Diode Laser Absorption Spectroscopy (TDLAS) and Mass Spectrometry (MC-ICP-MS), and their applications in research, including DNA studies and microbial analysis.
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NOTE: All labs do not provide the same QA/QC! NIST 1575 Pine run by 15 different labs Source: Jeff Owen, 2004
d13C values of plants are affected by / reflect: • moisture stress (e.g., Rundel and Sharifi, 1993, Stewart et al. 1995) • salinty (e.g., Guy et al. 1980) • light level (e.g., Ehleringer et al. 1986) • height in the canopy (e.g., Leavitt and Long 1982, McDowell et al. 2005) • lifespan (e.g., Ehleringer et al. 1993)
… because • When stomates relatively closed, ci low and Δ approaches 4.4 ‰; • if wide open, Δ 27‰ source unknown (oops)
Part 3: Advances in technology • TDL • MC-ICP-MS (for iron) • SIP (DNA studies) • SIMS • NMR • PLFA (microbial)
The math for a Keeling plot Cz = Ca – Cb Czdz = Cada – Cbdb Czdz = Cada – [(Ca-Cz)*db] Czdz = Cada – Cadb + Cz db Czdz = Ca(da – db) + Czdb Czdz – Czdb = Ca(da – db) Cz(dz – db) = Ca(da – db) dz – db = [Ca(da – db) ]/Cz dz = db + [Ca(da – db) ]/Cz A linear relationship; the intercept is the isotopic composition of the “source”
A Keeling plot integrates spatially Tu & Dawson, 2004
TDLAS = Tunable Diode Laser Absorption Spectroscopy A laser based system for measuring the mole fraction of a specific gas molecule Raw materials: Lead, Selenium, Sulfur End Product: About the size of a pencil eraser! Bowling et al. (2003)
Tunable diode laser absorption spectroscopy • fast-response analyzer for carbon isotopes of CO2 • very narrow wavelength infrared absorption • 4.3594 (12CO2) and 4.3582 mm (13CO2) • 1 kW and liquid nitrogen required • operates at field site Bowling et al. (2003)
SIP: Principle • Add a 13C-labeled compound (15N, 2H) • Incubate • Extract and separate an informative biomolecule • Lipids (PLFA) • Nucleic acids (DNA or RNA) • Proteins (not yet used) • Analyze biomolecule
Depth Profile of δ13C through an AOM Aggregate Orphan et al. (2001) Science 293:484.
13C-PLFA: who is eating what Brant et al. 2006 SBB