scholarly journals Ecosystem model intercomparison of under‐ice and total primary production in the A rctic O cean

2016 ◽  
Vol 121 (1) ◽  
pp. 934-948 ◽  
Author(s):  
Meibing Jin ◽  
Ekaterina E. Popova ◽  
Jinlun Zhang ◽  
Rubao Ji ◽  
Daniel Pendleton ◽  
...  
1988 ◽  
Vol 45 (4) ◽  
pp. 731-737 ◽  
Author(s):  
Harold E. Welch ◽  
John K. Jorgenson ◽  
Martin F. Curtis

Chironomid emergence was quantified in four small lakes at Saqvaqjuac, N.W.T. (63°39′N), before and after lake fertilization. Emerging biomass responded immediately to increased phytoplankton production, reaching equilibrium the following year. Emergence from the reference lake was extremely variable, for no apparent reason. The emergence – phytoplankton production relationships found by Davies for the Experimental Lakes Area (~49°N) were generally valid for Saqvaqjuac lakes and Char Lake (74°42′), except that (1) biomass was better correlated than numbers because of increased mean size with increasing latitude and (2) total primary production was a better predictor than phytoplankton production alone because benthic photosynthesis increases with increasing latitude. Chironomid production seems to be a predictable function of total primary production throughout the latitudinal range of the small Canadian lakes examined.


2010 ◽  
Vol 67 (2) ◽  
pp. 278-287 ◽  
Author(s):  
Leah M. Domine ◽  
Michael J. Vanni ◽  
William H. Renwick

The concept of new and regenerated production has been used extensively in marine ecosystems but rarely in freshwaters. We assessed the relative importance of new and regenerated phosphorus (P) in sustaining phytoplankton production in Acton Lake, a eutrophic reservoir located in southwestern Ohio, USA. Sources of nutrients to the euphotic zone, including watershed loading, fluxes from sediments, and excretion by sediment-feeding fish (gizzard shad, Dorosoma cepedianum ), were considered sources of new P input that support new primary production and were quantified over the course of a growing season. Regenerated production was estimated by the difference between new and total primary production. New production represented 32%–53% of total primary production, whereas regenerated production represented 47%–68% of total primary production. P excretion by gizzard shad supplied 45%–74% of new P and 24% of P required for total production. In summary, fluxes of P from the watershed and those from sediment-feeding fish need to be considered in strategies to reduce eutrophication in reservoir ecosystems.


2020 ◽  
Author(s):  
Karin Kvale ◽  
David P. Keller ◽  
Wolfgang Koeve ◽  
Katrin J. Meissner ◽  
Chris Somes ◽  
...  

Abstract. We describe and test a new model of biological marine silicate cycling, implemented in the University of Victoria Earth System Climate Model (UVic ESCM) version 2.9. This new model adds diatoms, which are a key aspect of the biological carbon pump, to an existing ecosystem model. The new model performs well against important ocean biogeochemical indicators and captures the large-scale features of the marine silica cycle. Furthermore it is computationally efficient, allowing both fully-coupled, long-timescale transient simulations, as well as "offline" transport matrix spinups. We assess the fully-coupled model against modern ocean observations, the historical record since 1960, and a business-as-usual atmospheric CO2 forcing to the year 2300. The model simulates a global decline in net primary production (NPP) of 1.3 % having occurred since the 1960s, with the strongest declines in the tropics, northern mid-latitudes, and Southern Ocean. The simulated global decline in NPP reverses after the year 2100 (forced by the extended RCP CO2 concentration scenario), and NPP returns to pre-industrial rates by 2300. This recovery is dominated by increasing primary production in the Southern Ocean, mostly by calcifying phytoplankton. Large increases in calcifying phytoplankton in the Southern Ocean offset a decline in the low latitudes, producing a global net calcite export in 2300 that varies only slightly from pre-industrial rates. Diatoms migrate southward in our simulations, following the receding Antarctic ice front, but are out-competed by calcifiers across most of their pre-industrial Southern Ocean habitat. Global opal export production thus drops to 50 % of its pre-industrial value by 2300. Model nutrients phosphate, silicate, and nitrate build up along the Southern Ocean particle export pathway, but dissolved iron (for which ocean sources are held constant) increases in the upper ocean. This different behaviour of iron is attributed to a reduction of low-latitude NPP (and consequently, a reduction in both uptake and export and particle, including calcite, scavenging), an increase in seawater temperatures (raising the solubility of particle forms), and stratification that "traps" the iron near the surface. These results are meant to serve as a baseline for sensitivity assessments to be undertaken with this model in the future.


2014 ◽  
Vol 71 (1) ◽  
pp. 31-46 ◽  
Author(s):  
Steven Mackinson

When an ecosystem model of the North Sea is calibrated to data from multiple trophic levels, the model estimated the primary production required to support the food web correlates temporally with observed changes in sea temperature and nutrient levels, supporting evidence from empirical analyses. However, a different result is given from an alternative calibration using fish stock data only. The inference taken from the emergent primary production – temperature relationship and empirical data are that, on balance, there is stronger overall evidence to support the calibration constrained at multiple trophic levels. Two important implications of the findings are (i) that the relative importance of fishing and environmental effects is likely to be interpreted differently depending on the calibration approach and (ii) the contrasting model calibrations would give different responses to fishing policies. It raises questions regarding how to judge the performance (and credibility) of an ecosystem model and the critical importance of conducting empirical and modelling analyses in parallel. Adopting a combined approach to ecosystem modelling is an important step in the pursuit of operational and defensible tools to support the ecosystem approach to management.


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