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Dive into the research topics where Christopher D. Winn is active.

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Featured researches published by Christopher D. Winn.


Deep-sea Research Part Ii-topical Studies in Oceanography | 1996

Seasonal and interannual variability in primary production and particle flux at Station ALOHA

David M. Karl; James R. Christian; John E. Dore; Dale V. Hebel; Ricardo M. Letelier; Luis M. Tupas; Christopher D. Winn

A 5-year time-series study of primary production and euphotic-zone particle export in the subtropical North Pacific Ocean near Hawaii (Sta. ALOHA, 22°45′N, 158°W) with measurements collected at approximately monthly intervals has revealed significant variability in both ecosystem processes. Depth-integrated (0–200 m) primary production averaged 463 mg C m−2 day−1 (s = 156, n = 54) or 14.1 mol C m−2 year−1. This mean value is greater than estimates for the North Pacific Ocean gyre made prior to 1984, but conforms to data obtained since the advent of trace metal-clean techniques. Daily rates of primary productivity at Sta. ALOHA exhibited interannual variability including a nearly 3-year sustained increase during the period 1990–1992 that coincided with a prolonged El Nifio-Southern Oscillation (ENSO) event. Export production, defined as the particulate carbon (PC) flux measured at the 150 m reference depth, also varied considerably during the initial 5 years of the ongoing field experiment. The PC flux averaged 29 mg C m−2 day−1 (s = 11, n = 43) or 0.88 mol Cm−2 year−1. A 5-fold variation between the minimum and maximum fluxes, measured in any given year, was observed. During the first 3 years of this program (1989–1991), a pattern was resolved that included two major export events per annum one centered in late winter and the other in late summer. After 1991, export production exhibited a systematic decrease with time during the prolonged ENSO event. When expressed as a percentage of the contemporaneous primary production, PC export ranged from 2 to 16.9%, with a 5-year mean of 6.7% (s = 3.3, n = 40). Contrary to existing empirical models, contemporaneous primary production and PC flux were poorly correlated, and during the ENSO period they exhibited a significant inverse correlation. This unexpected decoupling of particle production and flux has numerous implications for oceanic biogeochemical cycles and for the response of the ocean to environmental perturbations.


Deep Sea Research Part A. Oceanographic Research Papers | 1984

Primary productivity and particle fluxes on a transect of the equator at 153°W in the Pacific Ocean

Peter R. Betzer; William J. Showers; Edward A. Laws; Christopher D. Winn; Giacomo R. DiTullio; Peter M Kroopnick

Abstract Primary productivity (14C) and mass flux measurements using a free-drifting sediment trap deployed at 900 m were made at four stations in the Pacific Ocean between 12°N and 6°S at 153°W. The latitudinal variations in productivity were consistent with historical patterns showing the equator as a zone of high production and the oligotrophic waters north of the equatorial region as an area of low productivity. The correlation coefficient between the two sets of independent measurements was 0.999, indicating that in this oceanic area the activity of the primary producers was closely related to the total mass flux. A re-examination of historical data suggests that the downward flux of particulate organic carbon varies in direct proportion to the quotient of surface primary production raised to the 1.4 power and depth raised to the 0.63 power.


Nature | 1997

Experimental determination of the organic carbon flux from open-ocean surface waters

Steven Emerson; P. Quay; David M. Karl; Christopher D. Winn; Luis M. Tupas; Michael R. Landry

The flux of biologically produced organic carbon from the euphotic zone of the ocean to the deep waters below—the ‘biological organic carbon pump’—is one of the main controls on the carbon dioxide partial pressure in the atmosphere. Accurate determination of this flux is therefore critically important for understanding the global carbon cycle and its response to climate change. Our goal is to assess how accurately the biological organic carbon pump can be determined at a single location and to constrain estimates of the global value. As there are no standards against which such environmental fluxes can be measured, we assess accuracy by comparing results from three independent experimental approaches for measuring the net annual export of organic carbon from the euphotic zone in the subtropical North Pacific Ocean near Hawaii. Mass balances of dissolved oxygen, inorganic carbon and organic carbon yield estimates of the organic carbon export flux of 2.7 ± 1.7, 1.6 ± 0.9 and 2.0 ± 0.9 mol C m−2 yr−1, respectively. These three estimates are not significantly different, and establish the present analytically attainable accuracy at this location to be about ±50%. If 2.0 mol C m−2 yr−1 is typical of the organic carbon export flux in the subtropical ocean, then this vast region, often considered to be a biological desert, may be responsible for up to half of the global-ocean biological organic carbon pump.


Global Biogeochemical Cycles | 1999

Anthropogenic CO2 inventory of the Indian Ocean

Christopher L. Sabine; Robert M. Key; Kenneth M. Johnson; Frank J. Millero; Alain Poisson; Jorge L. Sarmiento; Douglas W.R. Wallace; Christopher D. Winn

This study presents basin-wide anthropogenic CO2 inventory estimates for the Indian Ocean based on measurements from the World Ocean Circulation Experiment/Joint Global Ocean Flux Study global survey. These estimates employed slightly modified ΔC* and time series techniques originally proposed by Gruber et al. [1996] and Wallace [1995], respectively. Together, the two methods yield the total oceanic anthropogenic CO2 and the carbon increase over the past 2 decades. The highest concentrations and the deepest penetrations of anthropogenic carbon are associated with the Subtropical Convergence at around 30° to 40°S. With both techniques, the lowest anthropogenic CO2 column inventories are observed south of 50°S. The total anthropogenic CO2 inventory north of 35°S was 13.6±2 Pg C in 1995. The inventory increase since GEOSECS (Geochemical Ocean Sections Program) was 4.1±1 Pg C for the same area. Approximately 6.7±1 Pg C are stored in the Indian sector of the Southern Ocean, giving a total Indian Ocean inventory of 20.3 ±3 Pg C for 1995. These estimates are compared to anthropogenic CO2 inventories estimated by the Princeton ocean biogeochemistry model. The model predicts an Indian Ocean sink north of 35°S that is only 0.61–0.68 times the results presented here; while the Southern Ocean sink is nearly 2.6 times higher than the measurement-based estimate. These results clearly identify areas in the models that need further examination and provide a good baseline for future studies of the anthropogenic inventory.


Archive | 1992

Trichodesmium Blooms and New Nitrogen in the North Pacific Gyre

David M. Karl; Ricardo M. Letelier; Dale V. Hebel; David F. Bird; Christopher D. Winn

A method of protecting plant life from injury due to frost or sub-freezing temperatures which comprises applying to the plant an effective, but non-phytotoxic amount, having regard to the plant being treated of a compound of the formula: wherein R1 is lower-alkyl; R2 is selected from the group consisting of:


Deep-sea Research Part Ii-topical Studies in Oceanography | 1996

Seasonal and interannual variations in photosynthetic carbon assimilation at Station

Ricardo M. Letelier; John E. Dore; Christopher D. Winn; David M. Karl

Abstract Autotrophic carbon assimilation measurements using a trace metal-free 14 C technique were performed at near monthly intervals between 1988 and 1992 in the North Pacific subtropical gyre (U.S. JGOFS-WOCE Sta. ALOHA; 22°45′N, 158°00′W). Integrated photosynthetic values ranged from 127 to 1055 mg C m −2 day −1 while the average carbon assimilation number ( P B ), defined as carbon assimilation rate per unit chlorophyll a (chi a ), varied between 1.6 and 12 g C (g chl a ) −1 h -1 in the 0–45 m depth range. Consistently low P B values ( a ) −1 h −1 , averaged in the upper 45 m of the water column) were observed during the first 2 years of this study but increased to > 5 g C (g chl a ) −1 h −1 during 1991–1992. This rise in PB was not associated with an increase in chi a . Furthermore, it occurred during a period of increased water column stability. Reduction in ATP and (NO 3 − + NO 2 − ) concentrations in the upper euphotic zone suggests that nutrient injections due to mixing events were minor or absent after January 1991. Two non-exclusive hypotheses are presented to explain the rise of P B in the absence of an enhancement of inorganic nutrient fluxes from below the euphotic zone: (i) high P B values observed during 1991–1992 are indicative of phytoplankton growth being balanced as a result of a decrease in the variability of nutrient injection due to a reduction in the frequency of mixing events, and (ii) the rise of PB during 1991–1992 is caused by an ecosystem shift from nitrogen to phosphorus limitation. The stability of the water column during 1991–1992 may have increased the availability of reduced nitrogen relative to phosphorus due to the enhancement of nitrogen fixation. Because these hypotheses do not require an increase in algal biomass or elemental fluxes across the base of the euphotic zone to explain an increase in autotrophic carbon assimilation, they imply that nutrient dynamics within the euphotic zone of the North Pacific subtropical gyre need to be understood in order to interpret changes in P B and predict carbon fluxes.


Marine Chemistry | 1998

Rising surface ocean dissolved inorganic carbon at the Hawaii Ocean Time-series site

Christopher D. Winn; Yuan-Hui Li; Fred T. Mackenzie; David M. Karl

Abstract Surface ocean dissolved inorganic carbon (DIC) and titration alkalinity have been measured for 7 years as a part of the Hawaii Ocean Time-series (HOT) program. The time-series data set displays an interannual increase in the inventory of surface ocean DIC which we interpret as a response to increasing atmospheric carbon dioxide concentrations. The rate of increase in surface ocean DIC at the open ocean HOT site is approximately 1 μ mol kg −1 yr −1 with a 95% confidence interval of 0.72 to 1.37 μ mol kg −1 yr −1 . This accumulation rate is consistent with the rate of increase predicted from the rise in boundary layer p CO 2 .


Global Biogeochemical Cycles | 1995

Seasonal variability in the phytoplankton community of the North Pacific Subtropical Gyre

Christopher D. Winn; Lisa Campbell; James R. Christian; Ricardo M. Letelier; Dale V. Hebel; John E. Dore; Lance Fujieki; David M. Karl

Time series measurements of in situ fluorescence, extracted particulate chlorophyll a, primary productivity, extracted adenosine 5′-triphosphate, and fluorescence per cell, as measured by flow cytometry, demonstrate seasonal cycles in fluorescence and chlorophyll concentrations in the North Pacific Subtropical Gyre (22° 45′N, 158° 00′W). Two opposing cycles are evident. In the upper euphotic zone (0–50 m), chlorophyll a concentrations increase in winter, with a maximum in December, and decrease each summer, with a minimum in June or July. In contrast, chlorophyll a concentrations in the lower euphotic zone (100–175 m) increase in spring, with a maximum in May, and decline in fall, with a minimum in October or November. The winter increase in chlorophyll a concentration in the upper 50 m of the water column appears to be a consequence of photoadaptation in response to decreased average mixed-layer light intensity rather than a change in phytoplankton biomass. In the lower euphotic zone, however, the seasonal cycle in pigment concentration does reflect a change in the rate of primary production and in phytoplankton biomass as a consequence of increased light intensity in summer. These observations have important implications for phytoplankton dynamics in the subtropical oceans and for remote sensing of phytoplankton biomass.


Deep-sea Research Part Ii-topical Studies in Oceanography | 2001

Consistency and synthesis of Pacific Ocean CO2 survey data

Marilyn F. Lamb; Christopher L. Sabine; Richard A. Feely; R. Wanninkhof; Robert M. Key; Gregory C. Johnson; Frank J. Millero; Kitack Lee; T.-H. Peng; Alexander Kozyr; John L. Bullister; Dana Greeley; Robert H. Byrne; David W. Chipman; Andrew G. Dickson; Catherine Goyet; Peter R. Guenther; Masayoshi Ishii; Kenneth M. Johnson; Charles D. Keeling; Tsueno Ono; K. Shitashima; Bronte Tilbrook; Taro Takahashi; Douglas W.R. Wallace; Yutaka W. Watanabe; Christopher D. Winn; C. S. Wong

Between 1991 and 1999, carbon measurements were made on twenty-five WOCE/JGOFS/OACES cruises in the Pacific Ocean. Investigators from 15 different laboratories and four countries analyzed at least two of the four measurable ocean carbon parameters (DIC, TAlk, fCO2, and pH) on almost all cruises. The goal of this work is to assess the quality of the Pacific carbon survey data and to make recommendations for generating a unified data set that is consistent between cruises. Several different lines of evidence were used to examine the consistency, including comparison of calibration techniques, results from certified reference material analyses, precision of at-sea replicate analyses, agreement between shipboard analyses and replicate shore based analyses, comparison of deep water values at locations where two or more cruises overlapped or crossed, consistency with other hydrographic parameters, and internal consistency with multiple carbon parameter measurements. With the adjustments proposed here, the data can be combined to generate a Pacific Ocean data set, with over 36,000 unique sample locations analyzed for at least two carbon parameters in most cases. The best data coverage was for DIC, which has an estimated overall accuracy of ∼3 μmol kg−1. TAlk, the second most common carbon parameter analyzed, had an estimated overall accuracy of ∼5 μmol kg−1. To obtain additional details on this study, including detailed crossover plots and information on the availability of the compiled, adjusted data set, visit the Global Data Analysis Project web site at: http://cdiac.esd.ornl.gov/oceans/glodap.


Global Biogeochemical Cycles | 1994

Air-sea carbon dioxide exchange in the North Pacific subtropical Gyre: Implications for the global carbon budget

Christopher D. Winn; Fred T. Mackenzie; Christopher J. Carrillo; Christopher L. Sabine; David M. Karl

The role of the ocean as a sink for anthropogenic carbon dioxide is a subject of intensive investigation and debate. Interest in this process is driven by the need to predict the rate of future increase of atmospheric carbon dioxide and subsequent global climatic change. Although estimates of the magnitude of the oceanic sink for carbon dioxide appear to be converging on a value of ∼2 (Gt) C yr−1 for the 1980s, a detailed understanding of the temporal and spatial variability in the rate of exchange of carbon dioxide between the ocean and the atmosphere is not available. For example, recent modeling work and direct measurements of air-sea carbon dioxide flux produce very different estimates of the air-sea flux in the northern hemisphere. As a consequence, it has been suggested that a large unidentified oceanic carbon dioxide sink may exist in the North Pacific. As a part of our time series observations in the North Pacific Subtropical Gyre, we have measured dissolved inorganic carbon and titration alkalinity over a four-year period. These measurements constitute the most extensive set of observations of carbon system parameters in the surface waters of the central Pacific Ocean. Our results show that the ocean in the vicinity of the time series site is a sink for atmospheric carbon dioxide. On the basis of these observations, we present a mechanism by which the North Pacific Subtropical Gyre can be a potential sink for ∼0.2 Gt C yr−1 of atmospheric carbon dioxide. Although our observations indicate that the North Pacific Subtropical Gyre is a sink for atmospheric carbon dioxide, the magnitude of this oceanic sink is relatively small. Our data and interpretations are therefore consistent with the argument for a relatively large sink during the 1980s in northern hemisphere terrestrial biomass. Another possibility is that the net release of carbon dioxide to the atmosphere owing to land use activities in tropical regions has been overestimated.

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Christopher L. Sabine

Pacific Marine Environmental Laboratory

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Fred T. Mackenzie

University of Hawaii at Manoa

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John E. Dore

Montana State University

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Kenneth M. Johnson

Brookhaven National Laboratory

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