1,081 research outputs found

    The magnitude of spring bacterial production in the North Atlantic Ocean

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    Dissolved organic carbon (DOC), a major reservoir in the ocean carbon cycle, is produced by a profusion of plankton sources and processes but is consumed mainly by bacterioplankton. Thus bacterial metabolism regulates the entry of DOC into the longer scale global carbon cycle. Bacterial production (BP) is the routinely measured quantity for evaluating the roles of bacteria in carbon cycling. However BP cannot be measured directly and instead is estimated from related metabolic processes requiring the use of poorly constrained conversion factors. BP and thus the total carbon utilization, are potentially uncertain by a factor of two or more. In the North Atlantic Bloom Experiment (NABE), BP was estimated to be about 30% of the simultaneous particulate primary production (PP), with some daily estimates exceeding 50%. Here we reassess these estimates, synthesizing knowledge and understanding of plankton dynamics gained since the 1989 NABE study. Daily BP derived from six different conversion factors averaged 20% of PP but ranged from 3 to 68%. The coupling of BP to PP was not consistent with either short-term cycling of labile DOC (hours) nor with much longer term cycling of semilabile DOC (seasons). Trophodynamic processes, including release of DOC from phytoplankton, by themselves could have maintained BP at about 15% of PP. Use of decomposing POC or previously accumulated semilabile DOC could each have supported some additional increment of BP for brief periods. Both reconsideration of observations and model results indicated that higher estimates of BP exceeding 20% of PP could not be supported without extraordinary and prolonged inputs of allochthonous carbon. Recent assertions of high BP in the tropics and other oceanic regimes should be considered carefully, especially if external subsidies are not obvious.Virginia Institute of Marine Scienc

    Ocean Biogeochemical Fluxes - New Production And Export Of Organic-Matter From The Upper Ocean

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    Studies of ocean biogeochemical fluxes have been energized in this decade, by the urgency of our need to understand and predict the effects of continued CO2accumulation in the atmosphere, by the global perspectives offered by satellite views of ocean color and related physical fields (McClain et al. 1991; Yoder et al. 1992; Mitchell 1994), and by the successful implementation of the Joint Global Ocean Flux Study (JGOFS; Bowles and Livingston, 1993). In this review, I focus on oceanic new production, originally defined as the fraction of primary production supported by inputs of ‘new’ nitrogen from outside the euphotic zone. With a growing appreciation of the role of this fundamental biogeochemical flux in the global carbon cycle, it has become more common to refer interchangeably to new production so defined, and to the export of organic matter from the upper ocean (e.g.. Sarmiento and Siegenthaler 1992). New production, the driving process of the ocean carbon cycle, is responsible for maintaining over half the vertical gradient in total inorganic carbon. In this review I refer to nitrate‐based new production in the open sea, and not to new production supported by other N compounds as observed in the coastal zone. Eppley (1992) gives a personal view of the modern formulation of the concept of equivalence between new production and upper ocean export. This review is dedicated to the memory of John Martin, a friend, colleague, leader and teacher who contributed mightily to our field.Virginia Institute of Marine Scienc

    Gluon fusion and bb¯ corrections to HW+W−/HZZ production in the POWHEG-BOX

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    AbstractThe study of the Higgs boson properties is one of the most important tasks to be accomplished in the next years, at the Large Hadron Collider (LHC) and at future colliders such as the Future Circular Collider in hadron–hadron mode (FCC-hh), the potential 100 TeV follow-up of the LHC machine. In this view the precise study of the Higgs couplings to weak gauge bosons is crucial and requires as much information as possible. After the recent calculation of the next-to-leading order QCD corrections to the production cross sections and differential distributions of a Standard Model Higgs boson in association with a pair of weak bosons, matched with parton shower in the POWHEG-BOX framework, we present the gluon fusion correction gg→HW+W−(HZZ) to the process pp→HW+W−(HZZ). This correction can be sizeable and amounts to +3% (+10%) in the HW+W− process and +5% (+18%) in the HZZ process at the LHC (FCC-hh). We also present the first study of the impact of the bottom-quark initiated channels bb¯→HW+W−/HZZ and find that they induce a significant +18% correction in the HW+W− channel at the FCC-hh. We present results on total cross sections and distributions at the LHC and at the FCC-hh

    Multi-scale variability of bacterioplankton abundance, production and specific growth rate in a temperate salt marsh tidal creek

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    [[sponsorship]]環境變遷研究中心[[note]]已出版;[SCI];有審查制度[[note]]http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=Drexel&SrcApp=hagerty_opac&KeyRecord=0024-3590&DestApp=JCR&RQ=IF_CAT_BOXPLO

    Temperature and substrate regulation of bacterial abundance, production and specific growth rate in temperate estuarine ecosystems

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    [[sponsorship]]環境變遷研究中心[[note]]已出版;[SCI];有審查制度[[note]]http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=Drexel&SrcApp=hagerty_opac&KeyRecord=0171-8630&DestApp=JCR&RQ=IF_CAT_BOXPLO

    Bacterioplankton growth responses to temperature and chlorophyll variations in estuaries measured by thymidine:leucine incorporation ratio

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    To identify the biochemical response of heterotrophic bacterioplankton to changing environmental conditions, seasonal and diel cycles of bacterial protein and DNA synthesis rates were estimated in temperate estuarine habitats from H-3-leucine (Leu) and H-3-thymidine (TdR) incorporation rates. Several short-term temperature manipulation experiments (5 to 35 degrees C) and 2 mesocosm experiments were performed to examine the effects of temperature and substrate supply on the ratio of Leu:TdR, respectively. The molar ratio of Leu to TdR varied about 5-fold (5.6 to 29.5) in the field and the values of the ratio were lower and more constant during high temperature (>25 degrees C) and high chlorophyll a (>8.0 mu g l(-1)) periods. In the temperature manipulation experiments, the Leu:TdR ratio decreased as temperature increased. In the mesocosm experiments, the Leu:TdR ratio was negatively correlated with chlorophyll a concentrations and bacterial specific growth rates. We propose that changes toward less favorable environmental conditions (e.g. reductions in temperature or substrate supply in temperate estuaries) might reduce bacterial protein and DNA synthesis rates simultaneously. However, the former process may be favored to maximize survival and this might lead to a higher Leu:TdR ratio. Conversely, when environmental conditions turn favorable, both processes could be enhanced and bacteria might optimize DNA duplication over protein metabolism to maximize reproduction, resulting in lower Leu:TdR ratios. Our results further indicate the complementariness of H-3-thymidine and H-3-leucine incorporation measurements for understanding processes controlling bacterial production since the ratio of these 2 tracer methods varied independently with temperature and substrate supply.Virginia Institute of Marine Scienc

    Temperature regulation of heterotrophic bacterioplankton biomass, production and specific growth rate in the Chesapeake Bay

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    [[sponsorship]]環境變遷研究中心[[note]]已出版;[SCI];有審查制度[[note]]http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=Drexel&SrcApp=hagerty_opac&KeyRecord=0024-3590&DestApp=JCR&RQ=IF_CAT_BOXPLO

    Regulation of bacterioplankton abundance and growth rate by substrate supply and bacterivory: a mesocosm study

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    [[sponsorship]]環境變遷研究中心[[note]]已出版;[SCI];有審查制度[[note]]http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=Drexel&SrcApp=hagerty_opac&KeyRecord=0095-3628&DestApp=JCR&RQ=IF_CAT_BOXPLO
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