The external phosphorus (P) loading has been halved, but the P content in the water column and the area of anoxic bottoms in Baltic proper has increased during the last 30 years. This can be explained by a temporary internal source of dissolved inorganic phosphorus (DIP) that is turned on when the water above the bottom sediment becomes anoxic. A load-response model, explaining the evolution from 1980 to 2005, suggests that the average specific DIP flux from anoxic bottoms in the Baltic proper is about 2.3 g P m−2 year−1. This is commensurable with fluxes estimated in situ from anoxic bottoms in the open Baltic proper and from hydrographic data in the deep part of Bornholm Basin. Oxygenation of anoxic bottoms, natural or manmade, may quickly turn off the internal P source from anoxic bottoms. This new P-paradigm should have far-reaching implications for abatement of eutrophication in the Baltic proper.Electronic supplementary materialThe online version of this article (doi:10.1007/s13280-013-0441-3) contains supplementary material, which is available to authorized users.
Abstract. During the four most recent glacial cycles, atmospheric CO 2 during glacial maxima has been lowered by about 90-100 ppm with respect to interglacials. There is widespread consensus that most of this carbon was partitioned in the ocean. It is, however, still debated which processes were dominant in achieving this increased carbon storage. In this paper, we use an Earth system model of intermediate complexity to explore the sensitivity of ocean carbon storage to ocean circulation state. We carry out a set of simulations in which we run the model to pre-industrial equilibrium, but in which we achieve different states of ocean circulation by changing forcing parameters such as wind stress, ocean diffusivity and atmospheric heat diffusivity. As a consequence, the ensemble members also have different ocean carbon reservoirs, global ocean average temperatures, biological pump efficiencies and conditions for air-sea CO 2 disequilibrium. We analyse changes in total ocean carbon storage and separate it into contributions by the solubility pump, the biological pump and the CO 2 disequilibrium component. We also relate these contributions to differences in the strength of the ocean overturning circulation. Depending on which ocean forcing parameter is tuned, the origin of the change in carbon storage is different. When wind stress or ocean diapycnal diffusivity is changed, the response of the biological pump gives the most important effect on ocean carbon storage, whereas when atmospheric heat diffusivity or ocean isopycnal diffusivity is changed, the solubility pump and the disequilibrium component are also important and sometimes dominant. Despite this complexity, we obtain a negative linear relationship between total ocean carbon and the combined strength of the northern and southern overturning cells. This relationship is robust to different reservoirs dominating the response to different forcing mechanisms. Finally, we conduct a drawdown experiment in which we investigate the capacity for increased carbon storage by artificially maximising the efficiency of the biological pump in our ensemble members. We conclude that different initial states for an ocean model result in different capacities for ocean carbon storage due to differences in the ocean circulation state and the origin of the carbon in the initial ocean carbon reservoir. This could explain why it is difficult to achieve comparable responses of the ocean carbon pumps in model intercomparison studies in which the initial states vary between models. We show that this effect of the initial state is quantifiable. The drawdown experiment highlights the importance of the strength of the biological pump in the control state for model studies of increased biological efficiency.
Abstract. We develop and use a circulation model to estimate hydrographical and ecological changes in the isolated basin water of the Bornholm Basin. By pumping welloxygenated so-called winter water to the greatest depth, where it is forced to mix with the resident water, the rate of deepwater density reduction increases as well as the frequency of intrusions of new oxygen-rich deepwater. We show that pumping 1000 m 3 s −1 should increase the rates of water exchange and oxygen supply by 2.5 and 3 times, respectively. The CRV (cod reproduction volume), the volume of water in the isolated basin meeting the requirements for successful cod reproduction (S > 11, O 2 > 2 mL L −1 ), should every year be greater than 54 km 3 , which is an immense improvement, since it has been much less in certain years. Anoxic bottoms should no longer occur in the basin, and hypoxic events will become rare. This should permit extensive colonization of fauna on the earlier periodically anoxic bottoms. Increased biomass of benthic fauna should also mean increased food supply to economically valuable demersal fish like cod and flatfish. In addition, re-oxygenation of the sediments should lead to increased phosphorus retention by the sediments.
The ocean's ability to take up and store CO 2 is a key factor for understanding past and future climate variability. However, qualitative and quantitative understanding of surface-to-interior pathways, and how the ocean circulation affects the CO 2 uptake, is limited. Consequently, how changes in ocean circulation may influence carbon uptake and storage and therefore the future climate remains ambiguous. Here we quantify the roles played by ocean circulation and various water masses in the meridional redistribution of carbon. We do so by calculating streamfunctions defined in dissolved inorganic carbon (DIC) and latitude coordinates, using output from a coupled biogeochemical-physical model. By further separating DIC into components originating from the solubility pump and a residual including the biological pump, air-sea disequilibrium, and anthropogenic CO 2 , we are able to distinguish the dominant pathways of how carbon enters particular water masses. With this new tool, we show that the largest meridional carbon transport occurs in a pole-to-equator transport in the subtropical gyres in the upper ocean. We are able to show that this pole-to-equator DIC transport and the Atlantic meridional overturning circulation (AMOC)-related DIC transport are mainly driven by the solubility pump. By contrast, the DIC transport associated with deep circulation, including that in Antarctic bottom water and Pacific deep water, is mostly driven by the biological pump. As these two pumps, as well as ocean circulation, are widely expected to be impacted by anthropogenic changes, these findings have implications for the future role of the ocean as a climate-buffering carbon reservoir.
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