Manning
Cara C.
Manning
Cara C.
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ArticleImpact of recently upwelled water on productivity investigated using in situ and incubation-based methods in Monterey Bay(John Wiley & Sons, 2017-03-11) Manning, Cara C. ; Stanley, Rachel H. R. ; Nicholson, David P. ; Smith, Jason M. ; Pennington, Timothy ; Fewings, Melanie R. ; Squibb, Michael E. ; Chavez, Francisco P.Photosynthetic conversion of inline image to organic carbon and the transport of this carbon from the surface to the deep ocean is an important regulator of atmospheric inline image. To understand the controls on carbon fluxes in a productive region impacted by upwelling, we measured biological productivity via multiple methods during a cruise in Monterey Bay, California. We quantified net community production and gross primary production from measurements of inline image/Ar and inline image triple isotopes ( inline image), respectively. We simultaneously conducted incubations measuring the uptake of 14C, inline image, and inline image, and nitrification, and deployed sediment traps. At the start of the cruise (Phase 1) the carbon cycle was at steady state and the estimated net community production was 35(10) and 35(8) mmol C m−2 d−1 from inline image/Ar and 15N incubations, respectively, a remarkably good agreement. During Phase 1, net primary production was 96(27) mmol C m−2 d−1 from C uptake, and gross primary production was 209(17) mmol C m−2 d−1 from inline image. Later in the cruise (Phase 2), recently upwelled water with higher nutrient concentrations entered the study area, causing 14C and inline image uptake to increase substantially. Continuous inline image/Ar measurements revealed submesoscale variability in water mass structure and likely productivity in Phase 2 that was not evident from the incubations. These data demonstrate that inline image/Ar and inline image incubation-based NCP estimates can give equivalent results in an N-limited, coastal system, when the nonsteady state inline image fluxes are negligible or can be quantified.
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ArticleIdeas and perspectives: a strategic assessment of methane and nitrous oxide measurements in the marine environment(European Geosciences Union, 2020-11-26) Wilson, Samuel T. ; Al-Haj, Alia N. ; Bourbonnais, Annie ; Frey, Claudia ; Fulweiler, Robinson W. ; Kessler, John D. ; Marchant, Hannah K. ; Milucka, Jana ; Ray, Nicholas E. ; Suntharalingam, Parvadha ; Thornton, Brett F. ; Upstill-Goddard, Robert C. ; Weber, Thomas S. ; Arévalo-Martínez, Damian L. ; Bange, Hermann W. ; Benway, Heather M. ; Bianchi, Daniele ; Borges, Alberto V. ; Chang, Bonnie X. ; Crill, Patrick M. ; del Valle, Daniela A. ; Farías, Laura ; Joye, Samantha B. ; Kock, Annette ; Labidi, Jabrane ; Manning, Cara C. ; Pohlman, John W. ; Rehder, Gregor ; Sparrow, Katy J. ; Tortell, Philippe D. ; Treude, Tina ; Valentine, David L. ; Ward, Bess B. ; Yang, Simon ; Yurganov, Leonid N.In the current era of rapid climate change, accurate characterization of climate-relevant gas dynamics – namely production, consumption, and net emissions – is required for all biomes, especially those ecosystems most susceptible to the impact of change. Marine environments include regions that act as net sources or sinks for numerous climate-active trace gases including methane (CH4) and nitrous oxide (N2O). The temporal and spatial distributions of CH4 and N2O are controlled by the interaction of complex biogeochemical and physical processes. To evaluate and quantify how these mechanisms affect marine CH4 and N2O cycling requires a combination of traditional scientific disciplines including oceanography, microbiology, and numerical modeling. Fundamental to these efforts is ensuring that the datasets produced by independent scientists are comparable and interoperable. Equally critical is transparent communication within the research community about the technical improvements required to increase our collective understanding of marine CH4 and N2O. A workshop sponsored by Ocean Carbon and Biogeochemistry (OCB) was organized to enhance dialogue and collaborations pertaining to marine CH4 and N2O. Here, we summarize the outcomes from the workshop to describe the challenges and opportunities for near-future CH4 and N2O research in the marine environment.
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ArticleChanges in gross oxygen production, net oxygen production, and air-water gas exchange during seasonal ice melt in Whycocomagh Bay, a Canadian estuary in the Bras d'or Lake system(European Geosciences Union, 2019-09-05) Manning, Cara C. ; Stanley, Rachel H. R. ; Nicholson, David P. ; Loose, Brice ; Lovely, Ann ; Schlosser, Peter ; Hatcher, Bruce G.Sea ice is an important control on gas exchange and primary production in polar regions. We measured net oxygen production (NOP) and gross oxygen production (GOP) using near-continuous measurements of the O2∕Ar gas ratio and discrete measurements of the triple isotopic composition of O2, during the transition from ice-covered to ice-free conditions, in Whycocomagh Bay, an estuary in the Bras d'Or Lake system in Nova Scotia, Canada. The volumetric gross oxygen production was 5.4+2.8−1.6 mmol O2 m−3 d−1, similar at the beginning and end of the time series, and likely peaked at the end of the ice melt period. Net oxygen production displayed more temporal variability and the system was on average net autotrophic during ice melt and net heterotrophic following the ice melt. We performed the first field-based dual tracer release experiment in ice-covered water to quantify air–water gas exchange. The gas transfer velocity at >90 % ice cover was 6 % of the rate for nearly ice-free conditions. Published studies have shown a wide range of results for gas transfer velocity in the presence of ice, and this study indicates that gas transfer through ice is much slower than the rate of gas transfer through open water. The results also indicate that both primary producers and heterotrophs are active in Whycocomagh Bay during spring while it is covered in ice.
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ArticleQuantifying air-sea gas exchange using noble gases in a coastal upwelling zone(IOPScience, 2016) Manning, Cara C. ; Stanley, Rachel H. R. ; Nicholson, David P. ; Squibb, Michael E.The diffusive and bubble-mediated components of air-sea gas exchange can be quantified separately using time-series measurements of a suite of dissolved inert gases. We have evaluated the performance of four published air-sea gas exchange parameterizations using a five-day time-series of dissolved He, Ne, Ar, Kr, and Xe concentration in Monterey Bay, CA. We constructed a vertical model including surface air-sea gas exchange and vertical diffusion. Diffusivity was measured throughout the cruise from profiles of turbulent microstructure. We corrected the mixed layer gas concentrations for an upwelling event that occurred partway through the cruise. All tested parameterizations gave similar results for Ar, Kr, and Xe; their air-sea fluxes were dominated by diffusive gas exchange during our study. For He and Ne, which are less soluble, and therefore more sensitive to differences in the treatment of bubble-mediated exchange, the parameterizations gave widely different results with respect to the net gas exchange flux and the bubble flux. This study demonstrates the value of using a suite of inert gases, especially the lower solubility ones, to parameterize air-sea gas exchange.
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PresentationOpen Access : the Power of One (or, how one individual moved an institution toward adopting an open access policy)( 2016-10-25) Manning, Cara C.A presentation and discussion on the ongoing process to elevate open access in Woods Hole, sponsored by the MBLWHOI Library in observance of International Open Access week. Presented 25 October 2016 at the Smith Lab, Woods Hole Oceanographic Institution, Woods Hole, MA
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PreprintContinuous measurements of dissolved Ne, Ar, Kr, and Xe ratios with a field-deployable gas equilibration mass spectrometer( 2016-01-30) Manning, Cara C. ; Stanley, Rachel H. R. ; Lott, Dempsey E.Noble gases dissolved in natural waters are useful tracers for quantifying physical processes. Here, we describe a field-deployable gas equilibration mass spectrometer (GEMS) that provides continuous, real-time measurements of Ne, Ar, Kr, and Xe mole ratios in natural waters. Gas is equilibrated with a membrane contactor cartridge and measured with a quadrupole mass spectrometer, after in-line purification with reactive metal alloy getters. We use an electron energy of 35 V for Ne to eliminate isobaric interferences, and a higher electron energy for the other gases to improve sensitivity. The precision is 0.7 % or better and 1.0 % or better for all mole ratios when the instrument is installed in a temperature-controlled environment and a variable-temperature environment, respectively. In the lab, the accuracy is 0.9 % or better for all gas ratios using air as the only calibration standard. In the field (and/or at greater levels of disequilbrium), the accuracy is 0.7 % or better for Ne/Kr, Ne/Ar, and Ar/Kr, and 2.5 % or better for Ne/Xe, Ar/Xe, and Kr/Xe using air as the only calibration standard. The field accuracy improves to 0.6 % or better for Ne/Xe, Ar/Xe, and Kr/Xe when the data is calibrated using discrete water samples run on a laboratory-based mass spectrometer. The e-folding response time is 90–410 s. This instrument enables the collection of a large number of continuous, high-precision and accuracy noble gas measurements at substantially reduced cost and labor compared to laboratory-based methods. Introduction
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ArticleAn intercomparison of oceanic methane and nitrous oxide measurements(Copernicus Publications on behalf of the European Geosciences Union, 2018-10-05) Wilson, Samuel T. ; Bange, Hermann W. ; Arévalo-Martínez, Damian L. ; Barnes, Jonathan ; Borges, Alberto V. ; Brown, Ian ; Bullister, John L. ; Burgos, Macarena ; Capelle, David W. ; Casso, Michael A. ; de la Paz, Mercedes ; Farías, Laura ; Fenwick, Lindsay ; Ferrón, Sara ; Garcia, Gerardo ; Glockzin, Michael ; Karl, David M. ; Kock, Annette ; Laperriere, Sarah ; Law, Cliff S. ; Manning, Cara C. ; Marriner, Andrew ; Myllykangas, Jukka-Pekka ; Pohlman, John W. ; Rees, Andrew P. ; Santoro, Alyson E. ; Tortell, Philippe D. ; Upstill-Goddard, Robert C. ; Wisegarver, David P. ; Zhang, Gui-Ling ; Rehder, GregorLarge-scale climatic forcing is impacting oceanic biogeochemical cycles and is expected to influence the water-column distribution of trace gases, including methane and nitrous oxide. Our ability as a scientific community to evaluate changes in the water-column inventories of methane and nitrous oxide depends largely on our capacity to obtain robust and accurate concentration measurements that can be validated across different laboratory groups. This study represents the first formal international intercomparison of oceanic methane and nitrous oxide measurements whereby participating laboratories received batches of seawater samples from the subtropical Pacific Ocean and the Baltic Sea. Additionally, compressed gas standards from the same calibration scale were distributed to the majority of participating laboratories to improve the analytical accuracy of the gas measurements. The computations used by each laboratory to derive the dissolved gas concentrations were also evaluated for inconsistencies (e.g., pressure and temperature corrections, solubility constants). The results from the intercomparison and intercalibration provided invaluable insights into methane and nitrous oxide measurements. It was observed that analyses of seawater samples with the lowest concentrations of methane and nitrous oxide had the lowest precisions. In comparison, while the analytical precision for samples with the highest concentrations of trace gases was better, the variability between the different laboratories was higher: 36% for methane and 27% for nitrous oxide. In addition, the comparison of different batches of seawater samples with methane and nitrous oxide concentrations that ranged over an order of magnitude revealed the ramifications of different calibration procedures for each trace gas. Finally, this study builds upon the intercomparison results to develop recommendations for improving oceanic methane and nitrous oxide measurements, with the aim of precluding future analytical discrepancies between laboratories.
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ThesisInsight into chemical, biological, and physical processes in coastal waters from dissolved oxygen and inert gas tracers(Massachusetts Institute of Technology and Woods Hole Oceanographic Institution, 2017-02) Manning, Cara C.In this thesis, I use coastal measurements of dissolved O2 and inert gases to provide insight into the chemical, biological, and physical processes that impact the oceanic cycles of carbon and dissolved gases. Dissolved O2 concentration and triple isotopic composition trace net and gross biological productivity. The saturation states of inert gases trace physical processes, such as air-water gas exchange, temperature change, and mixing, that affect all gases. First, I developed a field-deployable system that measures Ne, Ar, Kr, and Xe gas ratios in water. It has precision and accuracy of 1 % or better, enables near-continuous measurements, and has much lower cost compared to existing laboratory-based methods. The system will increase the scientific community’s access to use dissolved noble gases as environmental tracers. Second, I measured O2 and five noble gases during a cruise in Monterey Bay, California. I developed a vertical model and found that accurately parameterizing bubble-mediated gas exchange was necessary to accurately simulate the He and Ne measurements. I present the first comparison of multiple gas tracer, incubation, and sediment trap-based productivity estimates in the coastal ocean. Net community production estimated from 15NO –3 uptake and O2/Ar gave equivalent results at steady state. Underway O2/Ar measurements revealed submesoscale variability that was not apparent from daily incubations. Third, I quantified productivity by O2 mass balance and air-water gas exchange by dual tracer (3He/SF6) release during ice melt in the Bras d’Or Lakes, a Canadian estuary. The gas transfer velocity at >90% ice cover was 6% of the rate for nearly ice-free conditions. Rates of volumetric gross primary production were similar when the estuary was completely ice-covered and ice-free, and the ecosystem was on average net autotrophic during ice melt and net heterotrophic following ice melt. I present a method for incorporating the isotopic composition of H2O into the O2 isotope-based productivity calculations, which increases the estimated gross primary production in this study by 46–97%. In summary, I describe a new noble gas analysis system and apply O2 and inert gas observations in new ways to study chemical, biological, and physical processes in coastal waters.
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ArticleRiver Inflow Dominates Methane Emissions in an Arctic Coastal System(American Geophysical Union, 2020-04-23) Manning, Cara C. ; Preston, Victoria Lynn ; Jones, Samantha F. ; Michel, Anna P. M. ; Nicholson, David P. ; Duke, Patrick J. ; Ahmed, Mohamed M. M. ; Manganini, Kevin ; Else, Brent G. T. ; Tortell, Philippe D.We present a year‐round time series of dissolved methane (CH4), along with targeted observations during ice melt of CH4 and carbon dioxide (CO2) in a river and estuary adjacent to Cambridge Bay, Nunavut, Canada. During the freshet, CH4 concentrations in the river and ice‐covered estuary were up to 240,000% saturation and 19,000% saturation, respectively, but quickly dropped by >100‐fold following ice melt. Observations with a robotic kayak revealed that river‐derived CH4 and CO2 were transported to the estuary and rapidly ventilated to the atmosphere once ice cover retreated. We estimate that river discharge accounts for >95% of annual CH4 sea‐to‐air emissions from the estuary. These results demonstrate the importance of resolving seasonal dynamics in order to estimate greenhouse gas emissions from polar systems.
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ArticleRevising estimates of aquatic gross oxygen production by the triple oxygen isotope method to incorporate the local isotopic composition of water(John Wiley & Sons, 2017-10-25) Manning, Cara C. ; Howard, Evan M. ; Nicholson, David P. ; Ji, Brenda Y. ; Sandwith, Zoe O. ; Stanley, Rachel H. R.Measurement of the triple oxygen isotope (TOI) composition of O2 is an established method for quantifying gross oxygen production (GOP) in natural waters. A standard assumption to this method is that the isotopic composition of H2O, the substrate for photosynthetic O2, is equivalent to Vienna standard mean ocean water (VSMOW). We present and validate a method for estimating the TOI composition of H2O based on mixing of local meteoric water and seawater H2O end-members, and incorporating the TOI composition of H2O into GOP estimates. In the ocean, GOP estimates based on assuming the H2O is equivalent to VSMOW can have systematic errors of up to 48% and in low-salinity systems, errors can be a factor of 2 or greater. In future TOI-based GOP studies, TOI measurements of O2 and H2O should be paired when the H2O isotopic composition is expected to differ from VSMOW.