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Jonathan Wynn

Publications and source records attributed to Jonathan Wynn.

5 recordsLinked to original sources

Sources, distributions and dynamics of dissolved organic matter in the Canada and Makarov Basins

A comprehensive survey of dissolved organic carbon (DOC) and chromophoric dissolved organic matter (CDOM) was conducted in the Canada and Makarov Basins and adjacent seas during 2010–2012 to investigate the dynamics of dissolved organic matter (DOM) in the Arctic Ocean. Sources and distributions of DOM in polar surface waters were very heterogeneous and closely linked to hydrological conditions. Canada Basin surface waters had relatively low DOC concentrations (69 ± 6 μmol L −1 ), CDOM absorption ( a 325 : 0.32 ± 0.07 m −1 ) and CDOM-derived lignin phenols (3 ± 0.4 nmol L −1 ), and high spectral slope values ( S 275–295 : 31.7 ± 2.3 μm −1 ), indicating minor terrigenous inputs and evidence of photochemical alteration in the Beaufort Gyre. By contrast, surface waters of the Makarov Basin had elevated DOC (108 ± 9 μmol L −1 ) and lignin phenol concentrations (15 ± 3 nmol L −1 ), high a 325 values (1.36 ± 0.18 m −1 ), and low S 275–295 values (22.8 ± 0.8 μm −1 ), indicating pronounced Siberian river inputs associated with the Transpolar Drift and minor photochemical alteration. Observations near the Mendeleev Plain suggested limited interactions of the Transpolar Drift with Canada Basin waters, a scenario favoring export of Arctic DOM to the North Atlantic. The influence of sea-ice melt on DOM was region-dependent, resulting in an increase (Beaufort Sea), a decrease (Bering-Chukchi Seas), and negligible change (deep basins) in surface DOC concentrations and a 325 values. Halocline structures differed between basins, but the Canada Basin upper halocline and Makarov Basin halocline were comparable in their average DOC (65–70 μmol L −1 ) and lignin phenol concentrations (3–4 nmol L −1 ) and S 275–295 values (22.9–23.7 μm −1 ). Deep-water DOC concentrations decreased by 6–8 μmol L −1 with increasing depth, water mass age, nutrient concentrations, and apparent oxygen utilization. Maximal estimates of DOC degradation rates (0.036–0.039 μmol L −1 yr −1 ) in the deep Arctic were lower than those in other ocean basins, possibly due to low water temperatures. DOC concentrations in bottom waters (>2500 m; 46 ± 2 μmol L −1 ) of the Canada and Makarov Basins were slightly lower than those reported for deep waters of the Eurasian Basin and Nordic Seas. Elevated a 325 values (by 10–20%) were observed near the seafloor, indicating biological activity in Arctic basin sediments.

Frontiers in Marine Science

Response of the Miliolid Archaias angulatus to simulated ocean acidification

A common, but not universal, effect of ocean acidification on benthic foraminifera is a reduction in the growth rate. The miliolid Archaias angulatus is a high-Mg (>4 mole% MgCO 3 ), symbiont-bearing, soritid benthic foraminifer that contributes to Caribbean reef carbonate sediments. A laboratory culture study assessed the effects of reduced pH on the growth of A. angulatus . We observed a statistically significant 50% reduction in the growth rate (p < 0.01), calculated from changes in maximum diameter, from 160 &mu;m/28 days in the pH 8.0/pCO 2 air 480 ppm control group to 80 &mu;m/28 days at a treatment level of pH 7.6/pCO 2 air 1328 ppm. Additionally, pseudopore area, &delta; 18 O values, and Mg/Ca ratio all increased, albeit slightly in the latter two variables. The reduction in growth rate indicates that under a high-CO 2 setting, future A. angulatus populations will consist of smaller adults. A model using the results of this study estimates that at pH 7.6 A. angulatus carbonate production in the South Florida reef tract and Florida Bay decreases by 85%, from 0.27 Mt/yr to 0.04 Mt/yr, over an area of 9,000 km 2 .

Journal of Foraminiferal Research

USGS Arctic Ocean Carbon Cruise 2012: Field Activity L-01-12-AR to collect carbon data in the Arctic Ocean, August-September 2012

From August 25 to September 27, 2012, the United States Coast Guard Cutter (USCGC) Healy was part of an Extended Continental Shelf Project to determine the limits of the extended continental shelf in the Arctic. On a non-interference basis, a USGS ocean acidification team participated on the cruise to collect baseline water data in the Arctic. The collection of data extended from coastal waters near Barrow, Alaska, to 83&deg;2'N., -175&deg;36'W., and southward back to coastal waters near Barrow and on to Dutch Harbor, Alaska. As a consequence, a number of hypotheses were tested and questions asked associated with ocean acidification, including: What is the saturation state for different parts of the basin? What factors drive the saturation state in the different parts of the basin? How does saturation state compare to other regions? How do the carbon fluxes compare in the different parts of the basin? What is the buffering capacity of the water (Revelle factor)? What kind of variability does carbon demonstrate in the Arctic (near shore versus offshore and diurnal)? During the cruise, underway continuous and discrete water samples were collected, and discrete water samples were collected at stations to document the carbonate chemistry of the Arctic waters and quantify the saturation state of seawater with respect to calcium carbonate. These data are critical for providing baseline information in areas where no data have existed prior and will also be used to test existing models and predict future trends.

Arctic Ocean

USGS Arctic Ocean carbon cruise 2010: field activity H-03-10-AR to collect carbon data in the Arctic Ocean, August - September 2010

Carbon dioxide (CO 2 ) in the atmosphere is absorbed at the surface of the ocean by reacting with seawater to form carbonic acid, a weak, naturally occurring acid. As atmospheric carbon dioxide increases, the concentration of carbonic acid in seawater also increases, causing a decrease in ocean pH and carbonate mineral saturation states, a process known as ocean acidification. The oceans have absorbed approximately 525 billion tons of carbon dioxide from the atmosphere, or about one-quarter to one-third of the anthropogenic carbon emissions released since the beginning of the Industrial Revolution (Sabine and others, 2004). Global surveys of ocean chemistry have revealed that seawater pH has decreased by about 0.1 units (from a pH of 8.2 to 8.1) since the 1700s due to absorption of carbon dioxide (Caldeira and Wickett, 2003; Orr and others, 2005; Raven and others, 2005). Modeling studies, based on Intergovernmental Panel on Climate Change (IPCC) CO 2 emission scenarios, predict that atmospheric carbon dioxide levels could reach more than 500 parts per million (ppm) by the middle of this century and 800 ppm by the year 2100, causing an additional decrease in surface water pH of 0.3 pH units. Ocean acidification is a global threat and is already having profound and deleterious effects on the geology, biology, chemistry, and socioeconomic resources of coastal and marine habitats (Raven and others, 2005; Ruttiman, 2006). The polar and sub-polar seas have been identified as the bellwethers for global ocean acidification.

Data Series

USGS Arctic Ocean carbon cruise 2011: field activity H-01-11-AR to collect carbon data in the Arctic Ocean, August - September 2011

Carbon dioxide (CO 2 ) in the atmosphere is absorbed at the surface of the ocean by reacting with seawater to form a weak, naturally occurring acid called carbonic acid. As atmospheric carbon dioxide increases, the concentration of carbonic acid in seawater also increases, causing a decrease in ocean pH and carbonate mineral saturation states, a process known as ocean acidification. The oceans have absorbed approximately 525 billion tons of carbon dioxide from the atmosphere, or about one-quarter to one-third of the anthropogenic carbon emissions released since the beginning of the Industrial Revolution (Sabine and others, 2004). Global surveys of ocean chemistry have revealed that seawater pH has decreased by about 0.1 units (from a pH of 8.2 to 8.1) since the 1700s due to absorption of carbon dioxide (Caldeira and Wickett, 2003; Orr and others, 2005; Raven and others, 2005). Modeling studies, based on Intergovernmental Panel on Climate Change (IPCC) CO 2 emission scenarios, predict that atmospheric carbon dioxide levels could reach more than 500 parts per million (ppm) by the middle of this century and 800 ppm by the year 2100, causing an additional decrease in surface water pH of 0.3 pH units. Ocean acidification is a global threat and is already having profound and deleterious effects on the geology, biology, chemistry, and socioeconomic resources of coastal and marine habitats (Raven and others, 2005; Ruttiman, 2006). The polar and sub-polar seas have been identified as the bellwethers for global ocean acidification.

Data Series