Stable oxygen isotope composition of plant tissue: a review

2007 ◽  
Vol 34 (2) ◽  
pp. 83 ◽  
Author(s):  
Margaret M. Barbour

With the development of rapid measurement techniques, stable oxygen isotope analysis of plant tissue is poised to become an important tool in plant physiological, ecological, paleoclimatic and forensic studies. Recent advances in mechanistic understanding have led to the improvement of process-based models that accurately predict variability in the oxygen isotope composition of plant organic material (δ18Op). δ18Op has been shown to reflect the isotope composition of soil water, evaporative enrichment in transpiring leaves, and isotopic exchange between oxygen atoms in organic molecules and local water in the cells in which organic molecules are formed. This review presents current theoretical models describing the influences on δ18Op, using recently published experimental work to outline strengths and weaknesses in the models. The potential and realised applications of the technique are described.

2017 ◽  
Vol 454 ◽  
pp. 25-37 ◽  
Author(s):  
Sen Yang ◽  
Mingjun Zhang ◽  
Shengjie Wang ◽  
Yangmin Liu ◽  
Fang Qiang ◽  
...  

2020 ◽  
Author(s):  
Manuel F. G. Weinkauf ◽  
Jeroen Groeneveld ◽  
Joanna Waniek ◽  
Torsten Vennemann ◽  
Martini Rossana

Author(s):  
Andrea Watzinger ◽  
Katharina Schott ◽  
Rebecca Hood‐Nowotny ◽  
Federica Tamburini ◽  
Laura Arppe ◽  
...  

2019 ◽  
Vol 104 (10) ◽  
pp. 1503-1520 ◽  
Author(s):  
Katharina Marger ◽  
Cindy Luisier ◽  
Lukas P. Baumgartner ◽  
Benita Putlitz ◽  
Barbara L. Dutrow ◽  
...  

Abstract A series of tourmaline reference materials are developed for in situ oxygen isotope analysis by secondary ion mass spectrometry (SIMS), which allow study of the tourmaline compositions found in most igneous and metamorphic rocks. The new reference material was applied to measure oxygen isotope composition of tourmaline from metagranite, meta-leucogranite, and whiteschist from the Monte Rosa nappe (Western Alps). The protolith and genesis of whiteschist are highly debated in the literature. Whiteschists occur as 10 to 50 m tube-like bodies within the Permian Monte Rosa granite. They consist of chloritoid, talc, phengite, and quartz, with local kyanite, garnet, tourmaline, and carbonates. Whiteschist tourmaline is characterized by an igneous core and a dravitic overgrowth (XMg > 0.9). The core reveals similar chemical composition and zonation as meta-leucogranitic tourmaline (XMg = 0.25, δ18O = 11.3–11.5‰), proving their common origin. Dravitic overgrowths in whiteschists have lower oxygen isotope compositions (8.9–9.5‰). Tourmaline in metagranite is an intermediate schorl-dravite with XMg of 0.50. Oxygen isotope data reveal homogeneous composition for metagranite and meta-leucogranite tourmalines of 10.4–11.3‰ and 11.0–11.9‰, respectively. Quartz inclusions in both meta-igneous rocks show the same oxygen isotopic composition as the quartz in the matrix (13.6–13.9‰). In whiteschist the oxygen isotope composition of quartz included in tourmaline cores lost their igneous signature, having the same values as quartz in the matrix (11.4–11.7‰). A network of small fractures filled with dravitic tourmaline can be observed in the igneous core and suggested to serve as a connection between included quartz and matrix, and lead to recrystallization of the inclusion. In contrast, the igneous core of the whiteschist tourmaline fully retained its magmatic oxygen isotope signature, indicating oxygen diffusion is extremely slow in tourmaline. Tourmaline included in high-pressure chloritoid shows the characteristic dravitic overgrowth, demonstrating that chloritoid grew after the metasomatism responsible for the whiteschist formation, but continued to grow during the Alpine metamorphism. Our data on tourmaline and quartz show that tourmaline-bearing white-schists originated from the related meta-leucogranites, which were locally altered by late magmatic hydrothermal fluids prior to Alpine high-pressure metamorphism.


Author(s):  
Maggie Cusack ◽  
David Parkinson ◽  
Alberto Pérez-Huerta ◽  
Jennifer England ◽  
Gordon B. Curry ◽  
...  

ABSTRACTWith their extensive fossil record and shells of stable low-Mg calcite, rhynchonelliform brachiopods are attractive sources of climate information via seawater temperature proxies such as stable oxygen isotope composition. In Terebratalia transversa (Sowerby) there is a progression towards oxygen isotope equilibrium in the calcite of the innermost secondary layer. This study confirms the lack of any vital effects influencing oxygen isotope composition of T. transversa, even in specialised areas of the innermost secondary layer. Calcite Mg/Ca ratio is another potential seawater temperature proxy, that has the advantage of not being influenced by salinity. Mg concentrations measured by electron microprobe analyses indicate that there is no concomitant decrease in Mg concentration towards the inner secondary layer, associated with the progressive shift towards oxygen isotope equilibrium. Mg distribution is heterogeneous throughout the shell and correlates with that of sulphur, which may be a proxy for organic components, suggesting that some of the Mg may not be in the calcite lattice. It is essential therefore, to determine the chemical environment of the magnesium ions to avoid any erroneous temperature extrapolations in brachiopods or any other calcite biomineral.


2016 ◽  
Vol 16 (4) ◽  
pp. 2659-2673 ◽  
Author(s):  
Joël Savarino ◽  
William C. Vicars ◽  
Michel Legrand ◽  
Suzanne Preunkert ◽  
Bruno Jourdain ◽  
...  

Abstract. Variations in the stable oxygen isotope composition of atmospheric nitrate act as novel tools for studying oxidative processes taking place in the troposphere. They provide both qualitative and quantitative constraints on the pathways determining the fate of atmospheric nitrogen oxides (NO + NO2 = NOx). The unique and distinctive 17O excess (Δ17O = δ17O − 0.52 × δ18O) of ozone, which is transferred to NOx via oxidation, is a particularly useful isotopic fingerprint in studies of NOx transformations. Constraining the propagation of 17O excess within the NOx cycle is critical in polar areas, where there exists the possibility of extending atmospheric investigations to the glacial–interglacial timescale using deep ice core records of nitrate. Here we present measurements of the comprehensive isotopic composition of atmospheric nitrate collected at Dome C (East Antarctic Plateau) during the austral summer of 2011/2012. Nitrate isotope analysis has been here combined for the first time with key precursors involved in nitrate production (NOx, O3, OH, HO2, RO2, etc.) and direct observations of the transferrable Δ17O of surface ozone, which was measured at Dome C throughout 2012 using our recently developed analytical approach. Assuming that nitrate is mainly produced in Antarctica in summer through the OH + NO2 pathway and using concurrent measurements of OH and NO2, we calculated a Δ17O signature for nitrate on the order of (21–22 ± 3) ‰. These values are lower than the measured values that ranged between 27 and 31 ‰. This discrepancy between expected and observed Δ17O(NO3−) values suggests the existence of an unknown process that contributes significantly to the atmospheric nitrate budget over this East Antarctic region. However, systematic errors or false isotopic balance transfer functions are not totally excluded.


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