@article {2944,
	title = {A FRAMEWORK FOR TRANSDISCIPLINARY RADIOCARBON RESEARCH: USE OF NATURAL-LEVEL AND ELEVATED-LEVEL -14- C IN ANTARCTIC FIELD RESEARCHABSTRACT},
	journal = {Radiocarbon},
	volume = {63},
	year = {2021},
	month = {Jan-10-2021},
	pages = {1555 - 1568},
	abstract = {Radiocarbon (C-14) is an isotopic tracer used to address a wide range of scientific research questions. However, contamination by elevated levels of C-14 is deleterious to natural-level laboratory workspaces and accelerator mass spectrometer facilities designed to precisely measure small amounts of C-14. The risk of contaminating materials and facilities intended for natural-level C-14 with elevated-level C-14-labeled materials has dictated near complete separation of research groups practicing profoundly different measurements. Such separation can hinder transdisciplinary research initiatives, especially in remote and isolated field locations where both natural-level and elevated-level radiocarbon applications may be useful. This paper outlines the successful collaboration between researchers making natural-level C-14 measurements and researchers using C-14-labeled materials during a subglacial drilling project in West Antarctica (SALSA 2018-2019). Our strict operating protocol allowed us to successfully carry out C-14 labeling experiments within close quarters at our remote field camp without contaminating samples of sediment and water intended for natural level C-14 measurements. Here we present our collaborative protocol for maintaining natural level C-14 cleanliness as a framework for future transdisciplinary radiocarbon collaborations.},
	keywords = {AMS, contamination, LEUCINE, radiocarbon},
	issn = {0033-8222},
	doi = {10.1017/RDC.2021.55},
	url = {https://www.cambridge.org/core/product/identifier/S0033822221000552/type/journal_articlehttps://www.cambridge.org/core/services/aop-cambridge-core/content/view/S0033822221000552},
	author = {Venturelli, Ryan A and Vick-Majors, Trista J and Collins, Billy and Gagnon, Alan and Kasic, Kathy and Kurz, Mark D and Li, Wei and Priscu, John and Roberts, Mark and Rosenheim, Brad E}
}
@article { ISI:000268455600046,
	title = {Radiocarbon Analysis of Atmospheric Formaldehyde Using Cystamine Derivatization},
	journal = {ANALYTICAL CHEMISTRY},
	volume = {81},
	number = {{15}},
	year = {2009},
	month = {AUG 1},
	pages = {6310-6316},
	type = {Article},
	abstract = {A compound specific radiocarbon analysis method was developed to evaluate the C-14 composition of atmospheric formaldehyde. In this method, gaseous formaldehyde was collected with a high-volume air sampler using glass-fiber filters pretreated with sodium bisulfite. Collected formaldehyde was then released into water and derivatized with cysteamine to thiazolidine. The thiazolidine was extracted into dichloromethane and concentrated by evaporation. Concentrated thiazolidine was separated from other compounds using preparative capillary gas chromatography and uniquely collected as a phosphate salt with a fraction collector. The C-14 composition of the salt was analyzed by accelerator mass spectrometry after combustion to CO2 and subsequent reduction to graphite. In a pilot study, ambient formaldehyde samples collected on the roof of the CACS building at Narragansett Bay Campus, Narragansett, RI, showed a significantly larger fraction of fossil carbon than modern carbon.},
	issn = {0003-2700},
	doi = {10.1021/ac9004666},
	author = {Shen, Haiwei and McNichol, Ann P. and Xu, Li and Gagnon, Alan and Heikes, Brian G.}
}
