EARLY BOMB RADIOCARBON DETECTED IN PALAU ARCHIPELAGO CORALS Danielle Glynn 1,2 • Ellen Druffel 1 • Sheila Griffin 1 • Robert Dunbar 3 • Michael Osborne 3 • Joan Albert Sanchez-Cabeza 4 ABSTRACT. In order to evaluate the variability in surface water masses in the Western Pacific Warm Pool, we report high- precision radiocarbon measurements in annual and seasonal bands from Porites lutea corals collected from the Palau Archi- pelago (7N, 134E). Annual coral bands from 1945 to 2008 and seasonal samples from 1953 to 1957 were analyzed to cap- ture the initial early input of bomb 14 C from surface thermonuclear weapons testing in the Marshall Islands. Results show a pre-bomb average 14 C value of –54.9‰ between 1945 and early 1953. Beginning early in 1954, there is a rapid increase to a maximum of –23.1‰ at the start of 1955. Values continued to rise after 1957 to a post-bomb peak of 141‰ by 1976. The large initial rise in 14 C cannot be accounted for by air-sea CO 2 exchange. Results therefore suggest that the primary cause of this increase is the lateral advection of fallout-contaminated water from the Marshall Islands to Palau via the North Equa- torial Current and then to the North Equatorial Countercurrent. INTRODUCTION Atmospheric 14 CO 2 exchanges with CO 2 in the ocean to become part of the pool of dissolved inor- ganic carbon (DIC) in seawater. It takes approximately 10 yr for atmospheric 14 CO 2 to exchange with the surface ocean through air-sea gas exchange. The 14 C values then decrease with depth in the ocean due to decay and isolation from the atmospheric source of 14 C. Hermatypic, or reef-build- ing, corals that grow in the surface ocean incorporate DIC into their aragonitic skeletons and record the 14 C value of the surrounding seawater at the time of formation. Annual density bands, which are discernable when a coral slab is X-rayed, can be dated and used as proxies of past changes in water mass (Druffel and Linick 1978) and climate (Guilderson and Schrag 1998). Human-induced atmospheric injection of 14 C by thermonuclear bomb testing occurred during the 1950s and early 1960s (Yang et al. 2000). Global, regional, and local nuclear fallout sources have been observed in coral records. Ground-based nuclear explosions at Bikini Atoll (1135N, 16523E) turned coral, seawater, and other materials at the detonation site into reactive dust parti- cles containing higher 14 C values, known as “close-in fallout.” The surface nuclear explosion on 1 March 1954 at Bikini Atoll liberated and contaminated particles that eventually condensed into droplets that fell out of the atmosphere (Glasstone and Dolan 1977). Fallon and Guilderson (2008) observed a rapid rise of 14 C values in an Indonesian coral approximately 11 months after this nuclear detonation, suggesting that nuclear close-in fallout led to a more rapid absorption of 14 C into the water and coral than air-sea gas exchange alone. However, the processes by which this fallout was incorporated back into the environment are not well known. The Palau Archipelago lies in a complicated region of oceanic currents between the Philippine Sea and the Pacific. Tradewinds drive surface currents from east to west in the tropical Pacific, forming the North Equatorial Current (NEC). In the western Pacific, these waters then turn into the eastward- flowing North Equatorial Countercurrent (NECC), which brings water to Palau. The strength and position of both currents has been found to vary seasonally and show large interannual variability 1 Earth System Science Department, University of California, Irvine, Irvine, California 92697-3100, USA. author. Email: dglynn@uci.edu. 3 Department of Environmental Earth System Science, Stanford University, Stanford, California 94305-2115, USA. 4 Instituto de Ciencias del Mar y Limnologia, Universidad Nacional Autonoma de Mexico, 04510 Ciudad de Mexico, Mexico. 2 Corresponding © 2013 by the Arizona Board of Regents on behalf of the University of Arizona Proceedings of the 21st International Radiocarbon Conference edited by A J T Jull & C Hatte RADIOCARBON, Vol 55, Nr 2–3, 2013, p 1659–1664
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