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My strategy for writing this autobiography is to use examples of how working on seemingly different projects can often lead to outcomes more important than originally envisioned. Serendipity is a happy accident-specifically, the accident of discovering something useful without directly looking for it. This often occurs when two research projects converge unexpectedly. The main text contains examples of how serendipity has led me to important discoveries, including (a) finding surprisingly high 228Ra activities in the ocean; (b) developing a means of rapidly and quantitatively extracting radium from seawater; (c) devising a rapid, sensitive method of measuring 224Ra and 223Ra; (d) realizing the scale and biogeochemical importance of submarine groundwater discharge; and (e) conceiving a method to estimate the total flux of submarine groundwater discharge to the Atlantic Ocean. The Supplemental Material fleshes out details of these discoveries and places them in the context of my other investigations.
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Submarine groundwater discharge (SGD) supplies nutrients, carbon, metals, and radionuclide tracers to estuarine and coastal waters. One aspect of SGD that is poorly recognized is its direct effect on dissolved oxygen (DO) demand in receiving waters, denoted here as SGD-OD. Sulfate-mediated oxidation of organic matter in salty coastal aquifers produces numerous reduced byproducts including sulfide, ammonia, dissolved organic carbon and nitrogen, methane, and reduced metals. When these byproducts are introduced to estuarine and coastal systems by SGD and are oxidized, they may substantially reduce the DO concentration in receiving waters and impact organisms living there. We consider six estuarine and coastal sites where SGD derived fluxes of reduced byproducts are well documented. Using data from these sites we present a semiquantitative model to estimate the effect of these byproducts on DO in the receiving waters. Without continued aeration with atmospheric oxygen, the study sites would have experienced periodic hypoxic conditions due to SGD-OD. The presence of H2S supplied by SGD could also impact organisms. This process is likely prevalent in other systems worldwide.
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The shores of the Pearl River estuary are home to 35 million people. Their wastes are discharged into the large river delta-front estuary (LDE), one of the most highly polluted systems in the world. Here we construct a radium reactive transport model to estimate the terrestrial groundwater discharge (TGD) into the highly urbanized Pearl River LDE. We find the TGD comprises only approximately 0.9% in term of water discharge compared to the river discharge. The TGD in the Pearl River LDE delivers significant chemical fluxes to the coast, which are comparable to the fluvial loadings from Pearl River and other world major rivers. Of particular importance is the flux of ammonium because of its considerable role in Pearl River estuary eutrophication and hypoxia. Unlike the ammonium in many other aquifers, the ammonium in the Pearl River aquifer system is natural and originated from organic matter remineralization by sulfate reduction in the extremely reducing environment. The TGD derived NH4+ is as much as 5% of the upstream Pearl River fluvial loading and 42% of the anthropogenic inputs. This high groundwater NH4+ flux may greatly intensify the eutrophication, shift the trophic states, and lead to alarming hypoxia within the affected ecosystems in the Pearl River LDE. The large TGD derived chemical fluxes will lead to deterioration of water and will potentially affect human health.
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Estuários , Água Subterrânea/química , Rádio (Elemento)/análise , Compostos de Amônio/análise , China , Ecossistema , Monitoramento Ambiental , Eutrofização , Isótopos/análise , Rios/química , UrbanizaçãoRESUMO
Rising temperatures in the Arctic Ocean region are responsible for changes such as reduced ice cover, permafrost thawing, and increased river discharge, which, together, alter nutrient and carbon cycles over the vast Arctic continental shelf. We show that the concentration of radium-228, sourced to seawater through sediment-water exchange processes, has increased substantially in surface waters of the central Arctic Ocean over the past decade. A mass balance model for 228Ra suggests that this increase is due to an intensification of shelf-derived material inputs to the central basin, a source that would also carry elevated concentrations of dissolved organic carbon and nutrients. Therefore, we suggest that significant changes in the nutrient, carbon, and trace metal balances of the Arctic Ocean are underway, with the potential to affect biological productivity and species assemblages in Arctic surface waters.
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ABSTRACT: Large amounts of fission products were released from the Fukushima nuclear accident after a devastating earthquake and subsequent tsunami hit the northeast coast of Japan on 11 March 2011. The radioactive mass was sent high into the atmosphere by hydrogen explosions and fires in the reactor buildings at Fukushima Daiichi Nuclear Power Plant and spread all over the world. A relatively complete detection of both gaseous and particulate fission products was conducted during 15 March and 30 May 2011 at Orangeburg, South Carolina, located along the southeast coast of the United States, 11,000 km from the accident site. The histograms of gaseous and particulate radionuclides were obtained, and the major radioactivity plateaus were found between 18 March and 7 April 2011. The maximum levels of particulate and gaseous 131I were 1.0 ± 0.1 and 5.0 ± 0.4 mBq m-3, respectively. The maximum radioactivities of 134Cs and 137Cs were 10 times less than that of the particulate 131I. The average activity ratio of 134Cs to 137Cs was determined as 0.98 ± 0.26 throughout the observation. It was found that the plateaus and spikes in the histogram curves corresponded to the nuclear release events at Fukushima Daiichi. The arrival times of the particulate and gaseous nuclear fallout were determined to be 8 and 10 d, respectively. The deposition rates of gaseous and particulate iodine and the mass transfer between the two phases were discussed based on the radioactivity ratios of the fission products. By comparing with the radionuclide effluent concentrations issued in NRC 10 CFR 20, it was concluded that the Fukushima fallout presented negligible radiation risk to the public at Orangeburg as well as in the southeastern coastal region of the U.S.
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Tolo Harbour, located in the northeastern part of Hong Kong's New Territories, China, has a high frequency of algal blooms and red tides. An attempt was made to first quantify the submarine groundwater discharge (SGD) into Tolo Harbour using (226)Ra, and then to estimate the nutrient fluxes into the Harbour by this pathway. The total SGD was estimated to be 8.28×10(6) m(3) d(-1), while the fresh submarine groundwater discharge (FSGD) was estimated to be 2.31×10(5) m(3) d(-1). This showed that a large amount of SGD was contributed by recirculated seawater rather than fresh groundwater in the Harbour. Using the SGD and groundwater nutrient information around Tolo Harbour, the nutrient loading through SGD was estimated to be 1.1×10(6) mold(-1) for DIN, 1.4×10(4) mold(-1) for PO(4)(3-)-P and 1.4×10(6) mold(-1) for SiO(2)-Si, which was much more significant than its counterpart through the river discharge. Despite uncertainties in the estimation, the nutrient loading to Tolo Harbour by SGD is clearly significant. Thus, the current efforts for management of red tides in Tolo Harbour have to be reviewed and control of groundwater contamination is obviously required.
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The nutrient concentrations and stoichiometry in a coastal bay/estuary are strongly influenced by the direct riverine discharge and the submarine groundwater discharge (SGD). To estimate the fluxes of submarine groundwater discharge into the Bamen Bay (BB) and the Wanquan River Estuary (WQ) of eastern Hainan Island, China, the naturally occurring radium isotope ((226)Ra) was measured in water samples collected in the bay/estuary in August 2007 and 2008. Based on the distribution of (226)Ra in the surface water, a 3-end-member mixing model was used to estimate the relative contributions of the sources to these systems. Flushing times of 3.9±2.7 and 12.9±9.3 days were estimated for the BB and WQ, respectively, to calculate the radium fluxes for each system. Based on the radium fluxes from groundwater discharge and the Ra isotopic compositions in the groundwater samples, the estimated SGD fluxes were 3.4±5.0 m(3) s(-1) in the BB and 0.08±0.08 m(3) s(-1) in the WQ, or 16% and 0.06%, respectively, of the local river discharge. Using this information, the nutrient fluxes from the submarine groundwater discharge seeping into the BB and WQ regions were estimated. In comparison with the nutrient fluxes from the local rivers, the SGD-derived nutrient fluxes played a vital role in controlling the nutrient budgets and stoichiometry in the study area, especially in the BB.
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Monitoramento Ambiental , Água Subterrânea/química , China , Rádio (Elemento)/análise , Rios/química , Movimentos da ÁguaRESUMO
The exchange of groundwater between land and sea is a major component of the hydrological cycle. This exchange, called submarine groundwater discharge (SGD), is comprised of terrestrial water mixed with sea water that has infiltrated coastal aquifers. The composition of SGD differs from that predicted by simple mixing because biogeochemical reactions in the aquifer modify its chemistry. To emphasize the importance of mixing and chemical reaction, these coastal aquifers are called subterranean estuaries. Geologists recognize this mixing zone as a site of carbonate diagenesis and dolomite formation. Biologists have recognized that terrestrial inputs of nutrients to the coastal ocean may occur through subterranean processes. Further evidence of SGD comes from the distribution of chemical tracers in the coastal ocean. These tracers originate within coastal aquifers and reach the ocean through SGD. Tracer studies reveal that SGD provides globally important fluxes of nutrients, carbon, and metals to coastal waters.
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Água Doce/química , Fenômenos Geológicos , Movimentos da Água , Monitoramento Ambiental , Oceanos e Mares , Microbiologia da ÁguaRESUMO
The four naturally-occurring isotopes of radium were coupled with a previously evaluated hydrodynamic model to determine the apparent age of surface waters and to quantify submarine groundwater discharge (SGD) into the Venice Lagoon, Italy. Mean apparent age of water in the Venice Lagoon was calculated using the ratio of 224Ra to 228Ra determined from 30 monitoring stations and a mean pore water end member. Average apparent age was calculated to be 6.0 d using Ra ratios. This calculated age was very similar to average residence time calculated for the same period using a hydrodynamic model (5.8 d). A mass balance of Ra was accomplished by quantifying each of the sources and sinks of Ra in the lagoon, with the unknown variable being attributed to SGD. Total SGD were calculated to be 4.1 +/- 1.5, 3.8 +/- 0.7, 3.0 +/- 1.3, and 3.5 +/- 1.0 x 10(10) L d(-1) for (223,224,226, 228)Ra, respectively, which are an order of magnitude larger than total mean fluvial discharge into the Venice Lagoon (3.1 x 10(9) L d(-1)). The SGD as a source of nutrients in the Venice Lagoon is also discussed and, though significant to the nutrient budget, is likely to be less important as the dominant control on SGD is recirculated seawater rather than freshwater.