ALBERT

Description: In the last few decades, phytoplankton biomass has been commonly studied from space. However, satellite analysis of non-algal particles (NAPs), including heterotrophic bacteria and viruses, is relatively recent. In this work, we estimate the backscattering coefficient associated with the NAP fraction that does not covary with chlorophyll based on satellite particulate backscattering coefficient and chlorophyll (b bp NAP). b bp NAP is computed at 100-km resolution using 19 years of monthly satellite data. We find clear differences in b bp NAP between northern and southern oceans. High b bp NAP values are found in the Arctic and Southern Oceans, the North Atlantic area influenced by the Gulf Stream current, as well as shelf regions (i.e., Patagonian shelf) affected by upwelling regimes. Low correlation between chlorophyll and backscattering prevents precise b bp NAP estimations in oligotrophic areas (e.g., subtropical gyres). These b bp NAP estimations lead to a reduction to half in satellite-based phytoplankton biomass estimates respect to previously published results. ©2018. The Authors.

Description: Every year, about four percent of the plastic waste generated worldwide ends up in the ocean. What happens to the plastic there is poorly understood, though a growing body of evidence suggests it is rapidly spreading throughout the global ocean. The mechanisms of this spread are straightforward for buoyant larger plastics that can be accurately modelled using Lagrangian particle models. But the fate of the smallest size fractions (the microplastics) are less straightforward, in part because they can aggregate in sinking marine snow and faecal pellets. This biologically-mediated pathway is suspected to be a primary surface microplastic removal mechanism, but exactly how it might work in the real ocean is unknown. We search the parameter space of a new microplastic model embedded in an earth system model to show that biological uptake can significantly shape global microplastic inventory and distributions and even account for the budgetary “missing” fraction of surface microplastic, despite being an inefficient removal mechanism. While a lack of observational data hampers our ability to choose a set of “best” model parameters, our effort represents a first tool for quantitatively assessing hypotheses for microplastic interaction with ocean biology at the global scale.

Description: There is a longstanding discussion on how the macronutrient requirement of the export production in the North Atlantic subtropical gyre is sustained. In this study we asses the role of dissolved organic nitrogen (DON) and phosphorous (DOP) as sources of new nutrients into the North Atlantic subtropical gyre at 24.5° N. We define, based on measurements of DON, DOP, phytoplankton community structure, stable nitrogen isotopic signals, surface mixed layer depth and ocean color as viewed from space, four regions characterized by different nutrient supply regimes. Within these regions, two distinct loci of N2 fixation occur associated with different plankton assemblages and separated by a region in which N2 fixation occurs at levels insufficient to leave its distinctive isotopic fingerprint on the isotopic composition of PON. Here, the phosphorus supply pathways to the mixed plankton assemblage appear to be different. In the wester oligotrophic gyre (70–46° W), the lateral advection of DOP supplies the missing P that, together with, shallow mixed layer, almost permanent stratification and high water temperatures, stimulate diazotrophic growth, which augment TON local accumulation. In the eastern oligotophic gyre (46–30° W), DOP cannot support the P demand as it is exhausted on its way from productive areas. This is inferred from DOP turnover rates, estimated form enzymatic clevage rates, which are shorter (11 ± 8 months) than transit timescales, estimated from a 3-D circulation model (〉4 yr). A stronger seasonal cycle in chlorophyll and mixed layer depth, favour some nutrient injections from below. Here additional N sources come from the advected DON which has a turnover-time of 6.7 ± 3 yr, instead fast remineralization and little DOP export are needed to maintain the P requirements. We conclude from these observations that organic nutrient utilisation patterns drive diverse phytoplankton assemblages and oceanic nitrogen fixation gradients.

Description: The marine nitrogen (N) inventory is controlled by the interplay of nitrogen loss processes, here referred to as denitrification, and nitrogen source processes, primarily nitrogen fixation. The apparent stability of the marine N inventory on time scales longer than the estimated N residence time, suggests some intimate balance between N sinks and sources. Such a balance may be perceived easier to achieve when N sinks and sources occur in close spatial proximity, and some studies have interpreted observational evidence for such a proximity as indication for a stabilizing feedback processes. Using a biogeochemical ocean circulation model, we here show instead that a close spatial association of N2 fixation and denitrification can, in fact, trigger destabilizing feedbacks on the N inventory and, because of stoichiometric constrains, lead to net N losses. Contrary to current notion, a balanced N inventory requires a regional separation of N sources and sinks. This can be brought about by factors that reduce the growth of diazotrophs, such as iron, or by factors that affect the fate of the fixed nitrogen remineralization, such as dissolved organic matter dynamics. In light of our findings we suggest that spatial arrangements of N sinks and sources have to be accounted for in addition to individual rate estimates for reconstructing past, evaluating present and predicting future marine N inventory imbalances.

Description: To enable an accurate estimate of total excess nitrogen (N) in the North Atlantic a new tracer, TNxs, is defined which includes the contribution of organic nutrients to the assessment of N:P stoichiometric anomalies. We estimate the spatial distribution of TNxs within the North Atlantic using data from a trans-Atlantic section across 24.5° N conducted in 2004. We then employ three different approaches to infer rates of total excess nitrogen accumulation using pCFC-12 derived ventilation ages (a TNxs vertical integration, a one end-member and a two-end member mixing model). Despite some variability among the different methods the dissolved organic nutrient fraction always contributes to about half of the TNxs accumulation, which is in the order of 9.38±4.18×1011 mol N y−1. Here we suggest that neglecting organic nutrients in stoichiometric balances of the marine N and P inventories can lead to systematic errors when estimating a nitrogen excess or deficit relative to the Redfield ratio in the oceans. For the North Atlantic the inclusion of the organic fraction leads to an upward revision of the N supply by N2 fixation to 10.2±6.9×1011 mol N y−1. This enhanced estimate of nitrogen fixation reconciles the geochemical estimates of N2 fixation derived from excess nitrate and the direct estimates from N2 fixation measurements.

Description: Anthropogenic emissions of nitrogen (N) to the atmosphere have been strongly increasing during the last century, leading to greater atmospheric N deposition to the oceans. The North Atlantic subtropical gyre (NASTG) is particularly impacted. Here, upwind sources of anthropogenic N from North American and European sources have raised atmospheric N deposition to rates comparable with N2 fixation in the gyre. However, the biogeochemical fate of the deposited N is unclear because there is no detectable accumulation in the surface waters. Most likely, deposited N accumulates in the main thermocline instead, where there is a globally unique pool of N in excess of the canonical Redfield ratio of 16 N:1 phosphorus (P). To investigate this depth zone as a sink for atmospheric N, we used a biogeochemical ocean transport model and year 2000 nutrient deposition data. We examined the maximum effects of three mechanisms that may transport excess N from the ocean surface to the main thermocline: physical transport, preferential P remineralization of sinking particles, and nutrient uptake and export by phytoplankton at higher than Redfield N:P ratios. Our results indicate that atmospheric deposition may contribute 13–19% of the annual excess N input to the main thermocline. Modeled nutrient distributions in the NASTG were comparable to observations only when non-Redfield dynamics were invoked. Preferential P remineralization could not produce realistic results on its own; if it is an important contributor to ocean biogeochemistry, it must co-occur with N2 fixation. The results suggest that: 1) the main thermocline is an important sink for anthropogenic N deposition, 2) non-Redfield surface dynamics determine the biogeochemical fate of atmospherically deposited nutrients, and 3) atmospheric N accumulation in the main thermocline has long term impacts on surface ocean biology.

Description: Anthropogenic emissions of nitrogen (N) to the atmosphere have been strongly increasing during the last century, leading to greater atmospheric N deposition to the oceans. The North Atlantic subtropical gyre (NASTG) is particularly impacted. Here, upwind sources of anthropogenic N from North American and European sources have raised atmospheric N deposition to rates comparable with N2 fixation in the gyre. However, the biogeochemical fate of the deposited N is unclear because there is no detectable accumulation in the surface waters. Most likely, deposited N accumulates in the main thermocline instead, where there is a globally unique pool of N in excess of the canonical Redfield ratio of 16N:1 phosphorus (P). To investigate this depth zone as a sink for atmospheric N, we used a biogeochemical ocean transport model and year 2000 nutrient deposition data. We examined the maximum effects of three mechanisms that may transport excess N from the ocean surface to the main thermocline: physical transport, preferential P remineralization of sinking particles, and nutrient uptake and export by phytoplankton at higher than Redfield N:P ratios. Our results indicate that atmospheric deposition may contribute 13–19% of the annual excess N input to the main thermocline. Modeled nutrient distributions in the NASTG were comparable to observations only when non-Redfield dynamics were invoked. Preferential P remineralization could not produce realistic results on its own; if it is an important contributor to ocean biogeochemistry, it must co-occur with N2 fixation. The results suggest that: 1) the main thermocline is an important sink for anthropogenic N deposition, 2) non-Redfield surface dynamics determine the biogeochemical fate of atmospherically deposited nutrients, and 3) atmospheric N accumulation in the main thermocline has long term impacts on surface ocean biology.

Description: To enable an accurate estimate of total excess nitrogen (N) in the North Atlantic, a new tracer TNxs is defined, which includes the contribution of organic nutrients to the assessment of N:P stoichiometric anomalies. We measured the spatial distribution of TNxs within the subtropical North Atlantic using data from a trans-Atlantic section across 24.5° N occupied in 2004. We then employ three different approaches to infer rates of total excess nitrogen accumulation using pCFC-12 derived ventilation ages (a TNxs vertical integration, a one end-member and a two-end member mixing model). Despite some variability among the different methods the dissolved organic nutrient fraction always contributes to about half of the TNxs accumulation, which is in the order of 9.38±4.18×1011 mol N y−1. We suggest that neglecting organic nutrients in stoichiometric balances of the marine N and P inventories can lead to systematic errors when estimating deviations of nitrogen excess or deficit relative to the Redfield ratio in the oceans. For the North Atlantic the inclusion of the organic fraction to the excess nitrogen pool leads to an upward revision of the N supply by N2 fixation to 10.2±6.9×1011 mol N y−1.

Description: The marine nitrogen (N) inventory is thought to be stabilized by negative feedback mechanisms that reduce N inventory excursions relative to the more slowly overturning phosphorus inventory. Using a global biogeochemical ocean circulation model we show that negative feedbacks stabilizing the N inventory cannot persist if a close spatial association of N2 fixation and denitrification occurs. In our idealized model experiments, nitrogen deficient waters, generated by denitrification, stimulate local N2 fixation activity. But, because of stoichiometric constraints, the denitrification of newly fixed nitrogen leads to a net loss of N. This can enhance the N deficit, thereby triggering additional fixation in a vicious cycle, ultimately leading to a runaway N loss. To break this vicious cycle, and allow for stabilizing negative feedbacks to occur, inputs of new N need to be spatially decoupled from denitrification. Our idealized model experiments suggest that factors such as iron limitation or dissolved organic matter cycling can promote such decoupling and allow for negative feedbacks that stabilize the N inventory. Conversely, close spatial co-location of N2 fixation and denitrification could lead to net N loss.