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1
Mahowald, N., K. Lindsay, D. Rothenberg, S. C. Doney, J. K. Moore, P. Thornton, J. T. Randerson, and C. D. Jones. "Desert dust and anthropogenic aerosol interactions in the Community Climate System Model coupled-carbon-climate model." Biogeosciences Discussions 7, no. 5 (September 1, 2010): 6617–73. http://dx.doi.org/10.5194/bgd-7-6617-2010.
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Abstract. Coupled-carbon-climate simulations are an essential tool for predicting the impact of human activity onto the climate and biogeochemistry. Here we incorporate prognostic desert dust and anthropogenic aerosols into the CCSM3.1 coupled carbon-climate model and explore the resulting interactions with climate and biogeochemical dynamics through a series of transient anthropogenic simulations (20th and 21st centuries) and sensitivity studies. The inclusion of prognostic aerosols into this model has a small net global cooling effect on climate but does not significantly impact the globally averaged carbon cycle; we argue that this is likely to be because the CCSM3.1 model has a small climate feedback onto the carbon cycle. We propose a mechanism for including desert dust and anthropogenic aerosols into a simple carbon-climate feedback analysis to explain the results of our and previous studies. Inclusion of aerosols has statistically significant impacts on regional climate and biogeochemistry, in particular through the effects on the ocean nitrogen cycle and primary productivity of altered iron inputs from desert dust deposition.
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Mahowald, N., K. Lindsay, D. Rothenberg, S. C. Doney, J. K. Moore, P. Thornton, J. T. Randerson, and C. D. Jones. "Desert dust and anthropogenic aerosol interactions in the Community Climate System Model coupled-carbon-climate model." Biogeosciences 8, no. 2 (February 15, 2011): 387–414. http://dx.doi.org/10.5194/bg-8-387-2011.
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Abstract. Coupled-carbon-climate simulations are an essential tool for predicting the impact of human activity onto the climate and biogeochemistry. Here we incorporate prognostic desert dust and anthropogenic aerosols into the CCSM3.1 coupled carbon-climate model and explore the resulting interactions with climate and biogeochemical dynamics through a series of transient anthropogenic simulations (20th and 21st centuries) and sensitivity studies. The inclusion of prognostic aerosols into this model has a small net global cooling effect on climate but does not significantly impact the globally averaged carbon cycle; we argue that this is likely to be because the CCSM3.1 model has a small climate feedback onto the carbon cycle. We propose a mechanism for including desert dust and anthropogenic aerosols into a simple carbon-climate feedback analysis to explain the results of our and previous studies. Inclusion of aerosols has statistically significant impacts on regional climate and biogeochemistry, in particular through the effects on the ocean nitrogen cycle and primary productivity of altered iron inputs from desert dust deposition.
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Rodgers, K. B., O. Aumont, S. E. Mikaloff Fletcher, Y. Plancherel, L. Bopp, C. de Boyer Montégut, D. Iudicone, R. F. Keeling, G. Madec, and R. Wanninkhof. "Strong sensitivity of Southern Ocean carbon uptake and nutrient cycling to wind stirring." Biogeosciences Discussions 10, no. 9 (September 13, 2013): 15033–76. http://dx.doi.org/10.5194/bgd-10-15033-2013.
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Abstract. Here we test the hypothesis that winds have an important role in determining the rate of exchange of CO2 between the atmosphere and ocean through wind stirring over the Southern Ocean. This is tested with a sensitivity study using an ad hoc parameterization of wind stirring in an ocean carbon cycle model. The objective is to identify the way in which perturbations to the vertical density structure of the planetary boundary in the ocean impacts the carbon cycle and ocean biogeochemistry. Wind stirring leads to reduced uptake of CO2 by the Southern Ocean over the period 2000–2006, with differences of order 0.9 Pg C yr−1 over the region south of 45° S. Wind stirring impacts not only the mean carbon uptake, but also the phasing of the seasonal cycle of carbon and other species associated with ocean biogeochemistry. Enhanced wind stirring delays the seasonal onset of stratification, and this has large impacts on both entrainment and the biological pump. It is also found that there is a strong sensitivity of nutrient concentrations exported in Subantarctic Mode Water (SAMW) to wind stirring. This finds expression not only locally over the Southern Ocean, but also over larger scales through the impact on advected nutrients. In summary, the large sensitivity identified with the ad hoc wind stirring parameterization offers support for the importance of wind stirring for global ocean biogeochemistry, through its impact over the Southern Ocean.
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Hajima, Tomohiro, Michio Watanabe, Akitomo Yamamoto, Hiroaki Tatebe, Maki A. Noguchi, Manabu Abe, Rumi Ohgaito, et al. "Development of the MIROC-ES2L Earth system model and the evaluation of biogeochemical processes and feedbacks." Geoscientific Model Development 13, no. 5 (May 13, 2020): 2197–244. http://dx.doi.org/10.5194/gmd-13-2197-2020.
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Abstract. This article describes the new Earth system model (ESM), the Model for Interdisciplinary Research on Climate, Earth System version 2 for Long-term simulations (MIROC-ES2L), using a state-of-the-art climate model as the physical core. This model embeds a terrestrial biogeochemical component with explicit carbon–nitrogen interaction to account for soil nutrient control on plant growth and the land carbon sink. The model's ocean biogeochemical component is largely updated to simulate the biogeochemical cycles of carbon, nitrogen, phosphorus, iron, and oxygen such that oceanic primary productivity can be controlled by multiple nutrient limitations. The ocean nitrogen cycle is coupled with the land component via river discharge processes, and external inputs of iron from pyrogenic and lithogenic sources are considered. Comparison of a historical simulation with observation studies showed that the model could reproduce the transient global climate change and carbon cycle as well as the observed large-scale spatial patterns of the land carbon cycle and upper-ocean biogeochemistry. The model demonstrated historical human perturbation of the nitrogen cycle through land use and agriculture and simulated the resultant impact on the terrestrial carbon cycle. Sensitivity analyses under preindustrial conditions revealed that the simulated ocean biogeochemistry could be altered regionally (and substantially) by nutrient input from the atmosphere and rivers. Based on an idealized experiment in which CO2 was prescribed to increase at a rate of 1 % yr−1, the transient climate response (TCR) is estimated to be 1.5 K, i.e., approximately 70 % of that from our previous ESM used in the Coupled Model Intercomparison Project Phase 5 (CMIP5). The cumulative airborne fraction (AF) is also reduced by 15 % because of the intensified land carbon sink, which results in an airborne fraction close to the multimodel mean of the CMIP5 ESMs. The transient climate response to cumulative carbon emissions (TCRE) is 1.3 K EgC−1, i.e., slightly smaller than the average of the CMIP5 ESMs, which suggests that “optimistic” future climate projections will be made by the model. This model and the simulation results contribute to CMIP6. The MIROC-ES2L could further improve our understanding of climate–biogeochemical interaction mechanisms, projections of future environmental changes, and exploration of our future options regarding sustainable development by evolving the processes of climate, biogeochemistry, and human activities in a holistic and interactive manner.
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Heinze, M., and T. Ilyina. "Ocean Biogeochemistry in the warm climate of the Late Paleocene." Climate of the Past Discussions 10, no. 2 (April 28, 2014): 1933–75. http://dx.doi.org/10.5194/cpd-10-1933-2014.
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Abstract. The Late Paleocene is characterized by warm and stable climatic conditions which served as the background climate for the Paleocene-Eocene Thermal Maximum (PETM, ~55 million years ago). With respect to feedback processes in the carbon cycle, the ocean biogeochemical background state is of major importance for projecting the climatic response to a carbon perturbation related to the PETM. Therefore we use the Hamburg Ocean Carbon Cycle model HAMOCC, embedded into the ocean general circulation model of the Max Planck Institute for Meteorology, MPIOM, to constrain the ocean biogeochemistry of the Late Paleocene. We focus on the evaluation of modeled spatial and vertical distributions of the ocean carbon cycle parameters in a long-term warm steady-state ocean, based on a 560 ppm CO2 atmosphere. Model results are discussed in the context of available proxy data and simulations of pre-industrial conditions. Our results illustrate that ocean biogeochemistry is shaped by the warm and sluggish ocean state of the Late Paleocene, which affects the strength and spatial variation of the different carbon pumps. Primary production is only slightly reduced in comparison to present-day; it is intensified along the equator, especially in the Atlantic. This enhances remineralization of organic matter, resulting in strong oxygen minimum zones and CaCO3 dissolution in intermediate waters. We show that an equilibrium CO2 exchange without increasing total alkalinity concentrations above today's values is achieved. Yet, the surface ocean pH and the saturation state with respect to CaCO3 are lower than today. Our results indicate that under such conditions, the surface ocean carbonate chemistry is expected to be more sensitive to a carbon perturbation (i.e. the PETM) due to lower CO32− concentration, whereas the deep ocean calcite sediments would be less vulnerable to dissolution due to the sluggish ocean.
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Heinze, M., and T. Ilyina. "Ocean biogeochemistry in the warm climate of the late Paleocene." Climate of the Past 11, no. 1 (January 13, 2015): 63–79. http://dx.doi.org/10.5194/cp-11-63-2015.
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Abstract. The late Paleocene is characterized by warm and stable climatic conditions that served as the background climate for the Paleocene–Eocene Thermal Maximum (PETM, ~55 million years ago). With respect to feedback processes in the carbon cycle, the ocean biogeochemical background state is of major importance for projecting the climatic response to a carbon perturbation related to the PETM. Therefore, we use the Hamburg Ocean Carbon Cycle model (HAMOCC), embedded in the ocean general circulation model of the Max Planck Institute for Meteorology, MPIOM, to constrain the ocean biogeochemistry of the late Paleocene. We focus on the evaluation of modeled spatial and vertical distributions of the ocean carbon cycle parameters in a long-term warm steady-state ocean, based on a 560 ppm CO2 atmosphere. Model results are discussed in the context of available proxy data and simulations of pre-industrial conditions. Our results illustrate that ocean biogeochemistry is shaped by the warm and sluggish ocean state of the late Paleocene. Primary production is slightly reduced in comparison to the present day; it is intensified along the Equator, especially in the Atlantic. This enhances remineralization of organic matter, resulting in strong oxygen minimum zones and CaCO3 dissolution in intermediate waters. We show that an equilibrium CO2 exchange without increasing total alkalinity concentrations above today's values is achieved. However, consistent with the higher atmospheric CO2, the surface ocean pH and the saturation state with respect to CaCO3 are lower than today. Our results indicate that, under such conditions, the surface ocean carbonate chemistry is expected to be more sensitive to a carbon perturbation (i.e., the PETM) due to lower CO32− concentration, whereas the deep ocean calcite sediments would be less vulnerable to dissolution due to the vertically stratified ocean.
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Romanou, A., J. Romanski, and W. W. Gregg. "Natural ocean carbon cycle sensitivity to parameterizations of the recycling in a climate model." Biogeosciences Discussions 10, no. 7 (July 5, 2013): 11111–53. http://dx.doi.org/10.5194/bgd-10-11111-2013.
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Abstract. Sensitivities of the oceanic biological pump within the GISS climate modeling system are explored here. Results are presented from twin control simulations of the air-sea CO2 gas exchange using two different ocean models coupled to the same atmosphere. The two ocean models (Russell ocean model and Hybrid Coordinate Ocean Model, HYCOM) use different vertical coordinate systems, and therefore different representations of column physics. Both variants of the GISS climate model are coupled to the same ocean biogeochemistry module (the NASA Ocean Biogeochemistry Model, NOBM) which computes prognostic distributions for biotic and abiotic fields that influence the air-sea flux of CO2 and the deep ocean carbon transport and storage. In particular, the model differences due to remineralization rate changes are compared to differences attributed to physical processes modeled differently in the two ocean models such as ventilation, mixing, eddy stirring and vertical advection. The Southern Ocean emerges as a key region where the CO2 flux is as sensitive to biological parameterizations as it is to physical parameterizations. Mixing in the Southern Ocean is shown to be a~good indicator of the magnitude of the biological pump efficiency regardless of physical model choice.
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Butzin, Martin, Ying Ye, Christoph Völker, Özgür Gürses, Judith Hauck, and Peter Köhler. "Carbon isotopes in the marine biogeochemistry model FESOM2.1-REcoM3." Geoscientific Model Development 17, no. 4 (February 26, 2024): 1709–27. http://dx.doi.org/10.5194/gmd-17-1709-2024.
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Abstract. In this paper we describe the implementation of the carbon isotopes 13C and 14C (radiocarbon) into the marine biogeochemistry model REcoM3. The implementation is tested in long-term equilibrium simulations where REcoM3 is coupled with the ocean general circulation model FESOM2.1, applying a low-resolution configuration and idealized climate forcing. Focusing on the carbon-isotopic composition of dissolved inorganic carbon (δ13CDIC and Δ14CDIC), our model results are largely consistent with reconstructions for the pre-anthropogenic period. Our simulations also exhibit discrepancies, e.g. in upwelling regions and the interior of the North Pacific. Some of these differences are due to the limitations of our ocean circulation model setup, which results in a rather shallow meridional overturning circulation. We additionally study the accuracy of two simplified modelling approaches for dissolved inorganic 14C, which are faster (15 % and about a factor of five, respectively) than the complete consideration of the marine radiocarbon cycle. The accuracy of both simplified approaches is better than 5 %, which should be sufficient for most studies of Δ14CDIC.
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Keller, K. M., F. Joos, and C. C. Raible. "Time of emergence of trends in ocean biogeochemistry." Biogeosciences 11, no. 13 (July 9, 2014): 3647–59. http://dx.doi.org/10.5194/bg-11-3647-2014.
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Abstract. For the detection of climate change, not only the magnitude of a trend signal is of significance. An essential issue is the time period required by the trend to be detectable in the first place. An illustrative measure for this is time of emergence (ToE), that is, the point in time when a signal finally emerges from the background noise of natural variability. We investigate the ToE of trend signals in different biogeochemical and physical surface variables utilizing a multi-model ensemble comprising simulations of 17 Earth system models (ESMs). We find that signals in ocean biogeochemical variables emerge on much shorter timescales than the physical variable sea surface temperature (SST). The ToE patterns of pCO2 and pH are spatially very similar to DIC (dissolved inorganic carbon), yet the trends emerge much faster – after roughly 12 yr for the majority of the global ocean area, compared to between 10 and 30 yr for DIC. ToE of 45–90 yr are even larger for SST. In general, the background noise is of higher importance in determining ToE than the strength of the trend signal. In areas with high natural variability, even strong trends both in the physical climate and carbon cycle system are masked by variability over decadal timescales. In contrast to the trend, natural variability is affected by the seasonal cycle. This has important implications for observations, since it implies that intra-annual variability could question the representativeness of irregularly sampled seasonal measurements for the entire year and, thus, the interpretation of observed trends.
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Rodgers, K. B., O. Aumont, S. E. Mikaloff Fletcher, Y. Plancherel, L. Bopp, C. de Boyer Montégut, D. Iudicone, R. F. Keeling, G. Madec, and R. Wanninkhof. "Strong sensitivity of Southern Ocean carbon uptake and nutrient cycling to wind stirring." Biogeosciences 11, no. 15 (August 1, 2014): 4077–98. http://dx.doi.org/10.5194/bg-11-4077-2014.
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Abstract. Here we test the hypothesis that winds have an important role in determining the rate of exchange of CO2 between the atmosphere and ocean through wind stirring over the Southern Ocean. This is tested with a sensitivity study using an ad hoc parameterization of wind stirring in an ocean carbon cycle model, where the objective is to identify the way in which perturbations to the vertical density structure of the planetary boundary in the ocean impacts the carbon cycle and ocean biogeochemistry. Wind stirring leads to reduced uptake of CO2 by the Southern Ocean over the period 2000–2006, with a relative reduction with wind stirring on the order of 0.9 Pg C yr−1 over the region south of 45° S. This impacts not only the mean carbon uptake, but also the phasing of the seasonal cycle of carbon and other ocean biogeochemical tracers. Enhanced wind stirring delays the seasonal onset of stratification, and this has large impacts on both entrainment and the biological pump. It is also found that there is a strong reduction on the order of 25–30% in the concentrations of NO3 exported in Subantarctic Mode Water (SAMW) to wind stirring. This finds expression not only locally over the Southern Ocean, but also over larger scales through the impact on advected nutrients. In summary, the large sensitivity identified with the ad hoc wind stirring parameterization offers support for the importance of wind stirring for global ocean biogeochemistry through its impact over the Southern Ocean.
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Pasquier, Benoît, Mark Holzer, and Matthew A. Chamberlain. "The biological and preformed carbon pumps in perpetually slower and warmer oceans." Biogeosciences 21, no. 14 (July 24, 2024): 3373–400. http://dx.doi.org/10.5194/bg-21-3373-2024.
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Abstract. The marine carbon cycle is vitally important for climate and the fertility of the oceans. However, predictions of future biogeochemistry are challenging because a myriad of processes need parameterization and the future evolution of the physical ocean state is uncertain. Here, we embed a data-constrained model of the carbon cycle in slower and warmer ocean states as simulated under the RCP4.5 and RCP8.5 (RCP: Representative Concentration Pathway) scenarios for the 2090s and frozen in time for perpetuity. Focusing on steady-state changes from preindustrial conditions allows us to capture the response of the system integrated over all the timescales of the steady-state biogeochemistry, as opposed to typical transient simulations that capture only sub-centennial timescales. We find that biological production experiences only modest declines (of 8 %–12 %) because the reduced nutrient supply due to a more sluggish circulation and strongly shoaled mixed layers is counteracted by warming-stimulated growth. Organic-matter export declines by 15 %–25 % due to reductions in both biological production and export ratios, the latter being driven by warming-accelerated shallow respiration and reduced subduction of dissolved organic matter. The perpetual-2090s biological pump cycles a 30 %–70 % larger regenerated inventory accumulated over longer sequestration times, while preformed DIC is shunted away from biological utilization to outgassing. The regenerated and preformed DIC inventories both increase by a similar magnitude. We develop a conceptually new partitioning of preformed DIC to quantify the ocean's preformed carbon pump and its changes. Near-surface paths of preformed DIC are more important in the slower circulations, as weakened ventilation isolates the deep ocean. Thus, while regenerated DIC cycling becomes slower, preformed DIC cycling speeds up.
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Assmann, K. M., M. Bentsen, J. Segschneider, and C. Heinze. "An isopycnic ocean carbon cycle model." Geoscientific Model Development 3, no. 1 (February 16, 2010): 143–67. http://dx.doi.org/10.5194/gmd-3-143-2010.
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Abstract. The carbon cycle is a major forcing component in the global climate system. Modelling studies, aiming to explain recent and past climatic changes and to project future ones, increasingly include the interaction between the physical and biogeochemical systems. Their ocean components are generally z-coordinate models that are conceptually easy to use but that employ a vertical coordinate that is alien to the real ocean structure. Here, we present first results from a newly-developed isopycnic carbon cycle model and demonstrate the viability of using an isopycnic physical component for this purpose. As expected, the model represents well the interior ocean transport of biogeochemical tracers and produces realistic tracer distributions. Difficulties in employing a purely isopycnic coordinate lie mainly in the treatment of the surface boundary layer which is often represented by a bulk mixed layer. The most significant adjustments of the ocean biogeochemistry model HAMOCC, for use with an isopycnic coordinate, were in the representation of upper ocean biological production. We present a series of sensitivity studies exploring the effect of changes in biogeochemical and physical processes on export production and nutrient distribution. Apart from giving us pointers for further model development, they highlight the importance of preformed nutrient distributions in the Southern Ocean for global nutrient distributions. The sensitivity studies show that iron limitation for biological particle production, the treatment of light penetration for biological production, and the role of diapycnal mixing result in significant changes of nutrient distributions and liniting factors of biological production.
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Ussher, Simon J., Eric P. Achterberg, and Paul J. Worsfold. "Marine Biogeochemistry of Iron." Environmental Chemistry 1, no. 2 (2004): 67. http://dx.doi.org/10.1071/en04053.
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Environmental Context. Several trace elements are essential to the growth of microorganisms, iron being arguably the most important. Marine microorganisms, which affect the global carbon cycle and consequently indirectly influence the world’s climate, are therefore sensitive to the presence of iron. This link means iron-related oceanic processes are a significant ecological and political issue. Abstract. The importance of the role of iron as a limiting micronutrient for primary production in the World Ocean has become increasingly clear following large-scale in situ iron fertilization experiments in high-nutrient, low-chlorophyll (HNLC) regions.[1] This has led to intensive international research with the aim of understanding the marine biogeochemistry of iron and quantifying the spatial distribution and transport of the element in the oceans. Recent studies have benefited from improved trace metal handling protocols and sensitive analytical techniques, but uncertainties remain concerning fundamental processes such as redox transfer, solubility, adsorption, biological uptake, and remineralization. This review summarizes our present knowledge of iron biogeochemistry. It begins with a discussion of the effects of the physicochemical speciation of iron in seawater from a thermodynamic perspective, including important topics such as inorganic and organic complexation and redox chemistry. This is followed by an overview of the fluxes of iron to the ocean interface and a description of iron cycling within the open ocean water column. Current uncertainties of iron biogeochemistry are highlighted and suggestions of future work provided.
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Tagliabue, A., L. Bopp, D. M. Roche, N. Bouttes, J. C. Dutay, R. Alkama, M. Kageyama, E. Michel, and D. Paillard. "Quantifying the roles of ocean circulation and biogeochemistry in governing ocean carbon-13 and atmospheric carbon dioxide at the last glacial maximum." Climate of the Past 5, no. 4 (November 18, 2009): 695–706. http://dx.doi.org/10.5194/cp-5-695-2009.
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Abstract. We use a state-of-the-art ocean general circulation and biogeochemistry model to examine the impact of changes in ocean circulation and biogeochemistry in governing the change in ocean carbon-13 and atmospheric CO2 at the last glacial maximum (LGM). We examine 5 different realisations of the ocean's overturning circulation produced by a fully coupled atmosphere-ocean model under LGM forcing and suggested changes in the atmospheric deposition of iron and phytoplankton physiology at the LGM. Measured changes in carbon-13 and carbon-14, as well as a qualitative reconstruction of the change in ocean carbon export are used to evaluate the results. Overall, we find that while a reduction in ocean ventilation at the LGM is necessary to reproduce carbon-13 and carbon-14 observations, this circulation results in a low net sink for atmospheric CO2. In contrast, while biogeochemical processes contribute little to carbon isotopes, we propose that most of the change in atmospheric CO2 was due to such factors. However, the lesser role for circulation means that when all plausible factors are accounted for, most of the necessary CO2 change remains to be explained. This presents a serious challenge to our understanding of the mechanisms behind changes in the global carbon cycle during the geologic past.
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Tagliabue, A., L. Bopp, D. M. Roche, N. Bouttes, J. C. Dutay, R. Alkama, M. Kageyama, E. Michel, and D. Paillard. "Quantifying the roles of ocean circulation and biogeochemistry in governing ocean carbon-13 and atmospheric carbon dioxide at the last glacial maximum." Climate of the Past Discussions 5, no. 3 (May 20, 2009): 1463–91. http://dx.doi.org/10.5194/cpd-5-1463-2009.
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Abstract. We use a state-of-the-art ocean general circulation and biogeochemistry model to examine the impact of changes in ocean circulation and biogeochemistry in governing the change in ocean carbon-13 and atmospheric CO2 at the last glacial maximum (LGM). We examine 5 different realisations of the ocean's overturning circulation produced by a fully coupled atmosphere-ocean model under LGM forcing and suggested changes in the atmospheric deposition of iron and phytoplankton physiology at the LGM. Measured changes in carbon-13 and carbon-14, as well as a qualitative reconstruction of the change in ocean carbon export are used to evaluate the results. Overall, we find that while a reduction in ocean ventilation at the LGM is necessary to reproduce carbon-13 and carbon-14 observations, this circulation results in a low net sink for atmospheric CO2. In contrast, while biogeochemical processes contribute little to carbon isotopes, we can attribute over 90% of the change in atmospheric CO2 to such factors. The lesser role for circulation means that when all plausible factors are accounted for, over half of the necessary CO2 change remains to be explained. This presents a serious challenge to our understanding of the mechanisms behind changes in the global carbon cycle during the geologic past.
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Tjiputra, Jerry F., Jörg Schwinger, Mats Bentsen, Anne L. Morée, Shuang Gao, Ingo Bethke, Christoph Heinze, et al. "Ocean biogeochemistry in the Norwegian Earth System Model version 2 (NorESM2)." Geoscientific Model Development 13, no. 5 (May 26, 2020): 2393–431. http://dx.doi.org/10.5194/gmd-13-2393-2020.
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Abstract. The ocean carbon cycle is a key player in the climate system through its role in regulating the atmospheric carbon dioxide concentration and other processes that alter the Earth's radiative balance. In the second version of the Norwegian Earth System Model (NorESM2), the oceanic carbon cycle component has gone through numerous updates that include, amongst others, improved process representations, increased interactions with the atmosphere, and additional new tracers. Oceanic dimethyl sulfide (DMS) is now prognostically simulated and its fluxes are directly coupled with the atmospheric component, leading to a direct feedback to the climate. Atmospheric nitrogen deposition and additional riverine inputs of other biogeochemical tracers have recently been included in the model. The implementation of new tracers such as “preformed” and “natural” tracers enables a separation of physical from biogeochemical drivers as well as of internal from external forcings and hence a better diagnostic of the simulated biogeochemical variability. Carbon isotope tracers have been implemented and will be relevant for studying long-term past climate changes. Here, we describe these new model implementations and present an evaluation of the model's performance in simulating the observed climatological states of water-column biogeochemistry and in simulating transient evolution over the historical period. Compared to its predecessor NorESM1, the new model's performance has improved considerably in many aspects. In the interior, the observed spatial patterns of nutrients, oxygen, and carbon chemistry are better reproduced, reducing the overall model biases. A new set of ecosystem parameters and improved mixed layer dynamics improve the representation of upper-ocean processes (biological production and air–sea CO2 fluxes) at seasonal timescale. Transient warming and air–sea CO2 fluxes over the historical period are also in good agreement with observation-based estimates. NorESM2 participates in the Coupled Model Intercomparison Project phase 6 (CMIP6) through DECK (Diagnostic, Evaluation and Characterization of Klima) and several endorsed MIP simulations.
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Qu, Yang, Shamil Maksyutov, and Qianlai Zhuang. "Technical Note: An efficient method for accelerating the spin-up process for process-based biogeochemistry models." Biogeosciences 15, no. 13 (July 3, 2018): 3967–73. http://dx.doi.org/10.5194/bg-15-3967-2018.
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Abstract. To better understand the role of terrestrial ecosystems in the global carbon cycle and their feedbacks to the global climate system, process-based biogeochemistry models need to be improved with respect to model parameterization and model structure. To achieve these improvements, the spin-up time for those differential equation-based models needs to be shortened. Here, an algorithm for a fast spin-up was developed by finding the exact solution of a linearized system representing the cyclo-stationary state of a model and implemented in a biogeochemistry model, the Terrestrial Ecosystem Model (TEM). With the new spin-up algorithm, we showed that the model reached a steady state in less than 10 years of computing time, while the original method requires more than 200 years on average of model run. For the test sites with five different plant functional types, the new method saves over 90 % of the original spin-up time in site-level simulations. In North American simulations, average spin-up time savings for all grid cells is 85 % for either the daily or monthly version of TEM. The developed spin-up method shall be used for future quantification of carbon dynamics at fine spatial and temporal scales.
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Henson, Stephanie A. "Slow science: the value of long ocean biogeochemistry records." Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 372, no. 2025 (September 28, 2014): 20130334. http://dx.doi.org/10.1098/rsta.2013.0334.
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Sustained observations (SOs) have provided invaluable information on the ocean's biology and biogeochemistry for over 50 years. They continue to play a vital role in elucidating the functioning of the marine ecosystem, particularly in the light of ongoing climate change. Repeated, consistent observations have provided the opportunity to resolve temporal and/or spatial variability in ocean biogeochemistry, which has driven exploration of the factors controlling biological parameters and processes. Here, I highlight some of the key breakthroughs in biological oceanography that have been enabled by SOs, which include areas such as trophic dynamics, understanding variability, improved biogeochemical models and the role of ocean biology in the global carbon cycle. In the near future, SOs are poised to make progress on several fronts, including detecting climate change effects on ocean biogeochemistry, high-resolution observations of physical–biological interactions and greater observational capability in both the mesopelagic zone and harsh environments, such as the Arctic. We are now entering a new era for biological SOs, one in which our motivations have evolved from the need to acquire basic understanding of the ocean's state and variability, to a need to understand ocean biogeochemistry in the context of increasing pressure in the form of climate change, overfishing and eutrophication.
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Li, Tao, Laura F. Robinson, Tianyu Chen, Xingchen T. Wang, Andrea Burke, James W. B. Rae, Albertine Pegrum-Haram, et al. "Rapid shifts in circulation and biogeochemistry of the Southern Ocean during deglacial carbon cycle events." Science Advances 6, no. 42 (October 2020): eabb3807. http://dx.doi.org/10.1126/sciadv.abb3807.
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The Southern Ocean plays a crucial role in regulating atmospheric CO2 on centennial to millennial time scales. However, observations of sufficient resolution to explore this have been lacking. Here, we report high-resolution, multiproxy records based on precisely dated deep-sea corals from the Southern Ocean. Paired deep (∆14C and δ11B) and surface (δ15N) proxy data point to enhanced upwelling coupled with reduced efficiency of the biological pump at 14.6 and 11.7 thousand years (ka) ago, which would have facilitated rapid carbon release to the atmosphere. Transient periods of unusually well-ventilated waters in the deep Southern Ocean occurred at 16.3 and 12.8 ka ago. Contemporaneous atmospheric carbon records indicate that these Southern Ocean ventilation events are also important in releasing respired carbon from the deep ocean to the atmosphere. Our results thus highlight two distinct modes of Southern Ocean circulation and biogeochemistry associated with centennial-scale atmospheric CO2 jumps during the last deglaciation.
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Zaehle, S. "Terrestrial nitrogen–carbon cycle interactions at the global scale." Philosophical Transactions of the Royal Society B: Biological Sciences 368, no. 1621 (July 5, 2013): 20130125. http://dx.doi.org/10.1098/rstb.2013.0125.
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Interactions between the terrestrial nitrogen (N) and carbon (C) cycles shape the response of ecosystems to global change. However, the global distribution of nitrogen availability and its importance in global biogeochemistry and biogeochemical interactions with the climate system remain uncertain. Based on projections of a terrestrial biosphere model scaling ecological understanding of nitrogen–carbon cycle interactions to global scales, anthropogenic nitrogen additions since 1860 are estimated to have enriched the terrestrial biosphere by 1.3 Pg N, supporting the sequestration of 11.2 Pg C. Over the same time period, CO 2 fertilization has increased terrestrial carbon storage by 134.0 Pg C, increasing the terrestrial nitrogen stock by 1.2 Pg N. In 2001–2010, terrestrial ecosystems sequestered an estimated total of 27 Tg N yr −1 (1.9 Pg C yr −1 ), of which 10 Tg N yr −1 (0.2 Pg C yr −1 ) are due to anthropogenic nitrogen deposition. Nitrogen availability already limits terrestrial carbon sequestration in the boreal and temperate zone, and will constrain future carbon sequestration in response to CO 2 fertilization (regionally by up to 70% compared with an estimate without considering nitrogen–carbon interactions). This reduced terrestrial carbon uptake will probably dominate the role of the terrestrial nitrogen cycle in the climate system, as it accelerates the accumulation of anthropogenic CO 2 in the atmosphere. However, increases of N 2 O emissions owing to anthropogenic nitrogen and climate change (at a rate of approx. 0.5 Tg N yr −1 per 1°C degree climate warming) will add an important long-term climate forcing.
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Dall'Olmo, G., T. K. Westberry, M. J. Behrenfeld, E. Boss, C. Courties, L. Prieur, N. Hardman-Mountford, and T. Moutin. "Inferring phytoplankton carbon and eco-physiological rates from diel cycles of spectral particulate beam-attenuation coefficient." Biogeosciences Discussions 8, no. 2 (March 21, 2011): 3009–50. http://dx.doi.org/10.5194/bgd-8-3009-2011.
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Abstract. The diurnal fluctuations in solar irradiance impose a fundamental frequency on ocean biogeochemistry. Observations of the ocean carbon cycle at these frequencies are rare, but could be considerably expanded by measuring and interpreting the inherent optical properties. A method is presented to analyze diel cycles in particulate beam-attenuation coefficient (cp) measured at multiple wavelengths. The method is based on fitting observations with a size-structured population and optical model to infer the particle size distribution and physiologically relevant parameters of the cells responsible for the measured diel cycle in cp. Results show that the information related to size and contained in the spectral data can be exploited to independently estimate growth and loss rates during the day and night. In addition, the model can characterize the population of particles affecting the cp diel variability. Application of this method to spectral cp measured at a station in the oligotrophic Mediterranean Sea suggests that most of the observed variations in cp can be ascribed to a synchronized population of cells with an equivalent spherical diameter between 1 and 4 μm. The inferred carbon biomass of these cells was about 8–13 mg m−3 and accounted for approximately 20% of the total particulate organic carbon. If successfully validated and implemented on autonomous platforms, this method could improve our understanding of the ocean carbon cycle.
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Keller, K. M., F. Joos, and C. C. Raible. "Time of Emergence of trends in ocean biogeochemistry." Biogeosciences Discussions 10, no. 11 (November 20, 2013): 18065–92. http://dx.doi.org/10.5194/bgd-10-18065-2013.
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Abstract. For the detection of climate change, not only the magnitude of a trend signal is of significance. An essential issue is the time period required by the trend to be detectable in the first place. An illustrative measure for this is Time of Emergence (ToE), i.e., the point in time when a signal finally emerges from the background noise of natural variability. We investigate the ToE of trend signals in different biogeochemical and physical surface variables utilizing a multi-model ensemble comprising simulations of 17 ESMs. We find that signals in ocean biogeochemical variables emerge on much shorter timescales than the physical variable sea surface temperature (SST). The ToE patterns of pCO2 and pH are spatially very similar to DIC, yet the trends emerge much faster – after roughly 12 yr for the majority of the global ocean area, compared to between 10–30 yr for DIC and 45–90 yr for SST. In general, the background noise is of higher importance in determining ToE than the strength of the trend signal. In areas with high natural variability, even strong trends both in the physical climate and carbon cycle system are masked by variability over decadal timescales. In contrast to the trend, natural variability is affected by the seasonal cycle. This has important implications for observations, since it implies that intra-annual variability could question the representativeness of irregularly seasonal sampled measurements for the entire year and, thus, the interpretation of observed trends.
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Romanou, A., J. Romanski, and W. W. Gregg. "Natural ocean carbon cycle sensitivity to parameterizations of the recycling in a climate model." Biogeosciences 11, no. 4 (February 26, 2014): 1137–54. http://dx.doi.org/10.5194/bg-11-1137-2014.
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Abstract. Sensitivities of the oceanic biological pump within the GISS (Goddard Institute for Space Studies ) climate modeling system are explored here. Results are presented from twin control simulations of the air–sea CO2 gas exchange using two different ocean models coupled to the same atmosphere. The two ocean models (Russell ocean model and Hybrid Coordinate Ocean Model, HYCOM) use different vertical coordinate systems, and therefore different representations of column physics. Both variants of the GISS climate model are coupled to the same ocean biogeochemistry module (the NASA Ocean Biogeochemistry Model, NOBM), which computes prognostic distributions for biotic and abiotic fields that influence the air–sea flux of CO2 and the deep ocean carbon transport and storage. In particular, the model differences due to remineralization rate changes are compared to differences attributed to physical processes modeled differently in the two ocean models such as ventilation, mixing, eddy stirring and vertical advection. GISSEH(GISSER) is found to underestimate mixed layer depth compared to observations by about 55% (10%) in the Southern Ocean and overestimate it by about 17% (underestimate by 2%) in the northern high latitudes. Everywhere else in the global ocean, the two models underestimate the surface mixing by about 12–34%, which prevents deep nutrients from reaching the surface and promoting primary production there. Consequently, carbon export is reduced because of reduced production at the surface. Furthermore, carbon export is particularly sensitive to remineralization rate changes in the frontal regions of the subtropical gyres and at the Equator and this sensitivity in the model is much higher than the sensitivity to physical processes such as vertical mixing, vertical advection and mesoscale eddy transport. At depth, GISSER, which has a significant warm bias, remineralizes nutrients and carbon faster thereby producing more nutrients and carbon at depth, which eventually resurfaces with the global thermohaline circulation especially in the Southern Ocean. Because of the reduced primary production and carbon export in GISSEH compared to GISSER, the biological pump efficiency, i.e., the ratio of primary production and carbon export at 75 m, is half in the GISSEH of that in GISSER, The Southern Ocean emerges as a key region where the CO2 flux is as sensitive to biological parameterizations as it is to physical parameterizations. The fidelity of ocean mixing in the Southern Ocean compared to observations is shown to be a good indicator of the magnitude of the biological pump efficiency regardless of physical model choice.
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Jian, Jinshi, Rodrigo Vargas, Kristina Anderson-Teixeira, Emma Stell, Valentine Herrmann, Mercedes Horn, Nazar Kholod, et al. "A restructured and updated global soil respiration database (SRDB-V5)." Earth System Science Data 13, no. 2 (February 3, 2021): 255–67. http://dx.doi.org/10.5194/essd-13-255-2021.
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Abstract. Field-measured soil respiration (RS, the soil-to-atmosphere CO2 flux) observations were compiled into a global soil respiration database (SRDB) a decade ago, a resource that has been widely used by the biogeochemistry community to advance our understanding of RS dynamics. Novel carbon cycle science questions require updated and augmented global information with better interoperability among datasets. Here, we restructured and updated the global RS database to version SRDB-V5. The updated version has all previous fields revised for consistency and simplicity, and it has several new fields to include ancillary information (e.g., RS measurement time, collar insertion depth, collar area). The new SRDB-V5 includes published papers through 2017 (800 independent studies), where total observations increased from 6633 in SRDB-V4 to 10 366 in SRDB-V5. The SRDB-V5 features more RS data published in the Russian and Chinese scientific literature and has an improved global spatio-temporal coverage and improved global climate space representation. We also restructured the database so that it has stronger interoperability with other datasets related to carbon cycle science. For instance, linking SRDB-V5 with an hourly timescale global soil respiration database (HGRsD) and a community database for continuous soil respiration (COSORE) enables researchers to explore new questions. The updated SRDB-V5 aims to be a data framework for the scientific community to share seasonal to annual field RS measurements, and it provides opportunities for the biogeochemistry community to better understand the spatial and temporal variability in RS, its components, and the overall carbon cycle. The database can be downloaded at https://github.com/bpbond/srdb and will be made available in the Oak Ridge National Laboratory's Distributed Active Archive Center (ORNL DAAC). All data and code to reproduce the results in this study can be found at https://doi.org/10.5281/zenodo.3876443 (Jian and Bond-Lamberty, 2020).
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Wiltshire, Andrew J., Eleanor J. Burke, Sarah E. Chadburn, Chris D. Jones, Peter M. Cox, Taraka Davies-Barnard, Pierre Friedlingstein, et al. "JULES-CN: a coupled terrestrial carbon–nitrogen scheme (JULES vn5.1)." Geoscientific Model Development 14, no. 4 (April 27, 2021): 2161–86. http://dx.doi.org/10.5194/gmd-14-2161-2021.
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Abstract. Understanding future changes in the terrestrial carbon cycle is important for reliable projections of climate change and impacts on ecosystems. It is well known that nitrogen (N) could limit plants' response to increased atmospheric carbon dioxide and it is therefore important to include a representation of the N cycle in Earth system models. Here we present the implementation of the terrestrial nitrogen cycle in the Joint UK Land Environment Simulator (JULES) – the land surface scheme of the UK Earth System Model (UKESM). Two configurations are discussed – the first one (JULES-CN) has a bulk soil biogeochemical model and the second one is a development configuration that resolves the soil biogeochemistry with depth (JULES-CNlayer). In JULES the nitrogen (N) cycle is based on the existing carbon (C) cycle and represents all the key terrestrial N processes in a parsimonious way. Biological N fixation is dependent on net primary productivity, and N deposition is specified as an external input. Nitrogen leaves the vegetation and soil system via leaching and a bulk gas loss term. Nutrient limitation reduces carbon-use efficiency (CUE – ratio of net to gross primary productivity) and can slow soil decomposition. We show that ecosystem level N limitation of net primary productivity (quantified in the model by the ratio of the potential amount of C that can be allocated to growth and spreading of the vegetation compared with the actual amount achieved in its natural state) falls at the lower end of the observational estimates in forests (approximately 1.0 in the model compared with 1.01 to 1.38 in the observations). The model shows more N limitation in the tropical savanna and tundra biomes, consistent with the available observations. Simulated C and N pools and fluxes are comparable to the limited available observations and model-derived estimates. The introduction of an N cycle improves the representation of interannual variability of global net ecosystem exchange, which was more pronounced in the C-cycle-only versions of JULES (JULES-C) than shown in estimates from the Global Carbon Project. It also reduces the present-day CUE from a global mean value of 0.45 for JULES-C to 0.41 for JULES-CN and 0.40 for JULES-CNlayer, all of which fall within the observational range. The N cycle also alters the response of the C fluxes over the 20th century and limits the CO2 fertilisation effect, such that the simulated current-day land C sink is reduced by about 0.5 Pg C yr−1 compared to the version with no N limitation. JULES-CNlayer additionally improves the representation of soil biogeochemistry, including turnover times in the northern high latitudes. The inclusion of a prognostic land N scheme marks a step forward in functionality and realism for the JULES and UKESM models.
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Christian, James R., Kenneth L. Denman, Hakase Hayashida, Amber M. Holdsworth, Warren G. Lee, Olivier G. J. Riche, Andrew E. Shao, Nadja Steiner, and Neil C. Swart. "Ocean biogeochemistry in the Canadian Earth System Model version 5.0.3: CanESM5 and CanESM5-CanOE." Geoscientific Model Development 15, no. 11 (June 9, 2022): 4393–424. http://dx.doi.org/10.5194/gmd-15-4393-2022.
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Abstract. The ocean biogeochemistry components of two new versions of the Canadian Earth System Model (CanESM) are presented and compared to observations and other models. CanESM5 employs the same ocean biology model as CanESM2, whereas CanESM5-CanOE (Canadian Ocean Ecosystem model) is a new, more complex model developed for CMIP6, with multiple food chains, flexible phytoplankton elemental ratios, and a prognostic iron cycle. This new model is described in detail and the outputs (distributions of major tracers such as oxygen, dissolved inorganic carbon, and alkalinity, the iron and nitrogen cycles, plankton biomass, and historical trends in CO2 uptake and export production) compared to CanESM5 and CanESM2, as well as to observations and other CMIP6 models. Both CanESM5 models show gains in skill relative to CanESM2, which are attributed primarily to improvements in ocean circulation. CanESM5-CanOE shows improved skill relative to CanESM5 for most major tracers at most depths. CanESM5-CanOE includes a prognostic iron cycle, and maintains high-nutrient/low-chlorophyll conditions in the expected regions (in CanESM2 and CanESM5, iron limitation is specified as a temporally static “mask”). Surface nitrate concentrations are biased low in the subarctic Pacific and equatorial Pacific, and high in the Southern Ocean, in both CanESM5 and CanESM5-CanOE. Export production in CanESM5-CanOE is among the lowest for CMIP6 models; in CanESM5, it is among the highest, but shows the most rapid decline after about 1980. CanESM5-CanOE shows some ability to simulate aspects of plankton community structure that a single-species model can not (e.g. seasonal dominance of large cells) but is biased towards low concentrations of zooplankton and detritus relative to phytoplankton. Cumulative ocean uptake of anthropogenic carbon dioxide through 2014 is lower in both CanESM5-CanOE (122 PgC) and CanESM5 (132 PgC) than in observation-based estimates (145 PgC) or the model ensemble mean (144 PgC).
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Tang, Jinyun, and William J. Riley. "On the modeling paradigm of plant root nutrient acquisition." Plant and Soil 459, no. 1-2 (January 14, 2021): 441–51. http://dx.doi.org/10.1007/s11104-020-04798-5.
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AbstractPlant root nutrient acquisition, and to a lesser extent foliar nutrient uptake, maintain plant metabolism and strongly regulate terrestrial biogeochemistry and carbon-climate feedbacks. However, terrestrial biogeochemical models differ in their representations of plant root nutrient acquisition, leading to significantly different, and uncertain, carbon cycle and future climate projections. Here we first review biogeochemical principles and observations relevant to three essential plant root nutrient acquisition mechanisms: activity of nutrient acquiring proteins, maintenance of nutrient stoichiometry, and energy expenditure for these processes. We next examine how these mechanisms are considered in three existing modeling paradigms, and conclude by recommending the capacity-based approach, the need for observations, and necessary modeling developments of plant root nutrient acquisition to improve carbon-climate feedback projections.
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Rantala, Marttiina V., Carsten Meyer-Jacob, E. Henriikka Kivilä, Tomi P. Luoto, Antti E. K. Ojala, John P. Smol, and Liisa Nevalainen. "Traces of sunlight in the organic matter biogeochemistry of two shallow subarctic lakes." Biogeochemistry 155, no. 2 (June 18, 2021): 169–88. http://dx.doi.org/10.1007/s10533-021-00820-9.
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AbstractGlobal environmental change alters the production, terrestrial export, and photodegradation of organic carbon in northern lakes. Sedimentary biogeochemical records can provide a unique means to understand the nature of these changes over long time scales, where observational data fall short. We deployed in situ experiments on two shallow subarctic lakes with contrasting light regimes; a clear tundra lake and a dark woodland lake, to first investigate the photochemical transformation of carbon and nitrogen elemental (C/N ratio) and isotope (δ13C, δ15N) composition in lake water particulate organic matter (POM) for downcore inferences. We then explored elemental, isotopic, and spectral (inferred lake water total organic carbon [TOC] and sediment chlorophyll a [CHLa]) fingerprints in the lake sediments to trace changes in aquatic production, terrestrial inputs and photodegradation before and after profound human impacts on the global carbon cycle prompted by industrialization. POM pool in both lakes displayed tentative evidence of UV photoreactivity, reflected as increasing δ13C and decreasing C/N values. Through time, the tundra lake sediments traced subtle shifts in primary production, while the woodland lake carried signals of changing terrestrial contributions, indicating shifts in terrestrial carbon export but possibly also photodegradation rates. Under global human impact, both lakes irrespective of their distinct carbon regimes displayed evidence of increased productivity but no conspicuous signs of increased terrestrial influence. Overall, sediment biogeochemistry can integrate a wealth of information on carbon regulation in northern lakes, while our results also point to the importance of considering the entire spectrum of photobiogeochemical fingerprints in sedimentary studies.
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Matsumoto, K., K. Tokos, A. Huston, and H. Joy-Warren. "MESMO 2: a mechanistic marine silica cycle and coupling to a simple terrestrial scheme." Geoscientific Model Development 6, no. 2 (April 12, 2013): 477–94. http://dx.doi.org/10.5194/gmd-6-477-2013.
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Abstract. Here we describe the second version of Minnesota Earth System Model for Ocean biogeochemistry (MESMO 2), an earth system model of intermediate complexity, which consists of a dynamical ocean, dynamic-thermodynamic sea ice, and energy moisture balanced atmosphere. The new version has more realistic land ice masks and is driven by seasonal winds. A major aim in version 2 is representing the marine silica cycle mechanistically in order to investigate climate-carbon feedbacks involving diatoms, a critically important class of phytoplankton in terms of carbon export production. This is achieved in part by including iron, on which phytoplankton uptake of silicic acid depends. Also, MESMO 2 is coupled to an existing terrestrial model, which allows for the exchange of carbon, water and energy between land and the atmosphere. The coupled model, called MESMO 2E, is appropriate for more complete earth system simulations. The new version was calibrated, with the goal of preserving reasonable interior ocean ventilation and various biological production rates in the ocean and land, while simulating key features of the marine silica cycle.
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Matsumoto, K., K. S. Tokos, A. Huston, and H. Joy-Warren. "MESMO 2: a mechanistic marine silica cycle and coupling to a simple terrestrial scheme." Geoscientific Model Development Discussions 5, no. 3 (September 24, 2012): 2999–3033. http://dx.doi.org/10.5194/gmdd-5-2999-2012.
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Abstract. Here we describe the second version of Minnesota Earth System Model for Ocean biogeochemistry (MESMO 2), an earth system model of intermediate complexity, which consists of a dynamical ocean, dynamic-thermodynamic sea ice, and energy moisture balanced atmosphere. The new version has more realistic land ice masks and is driven by seasonal winds. A major aim in version 2 is representing the marine silica cycle mechanistically in order to investigate climate-carbon feedbacks involving diatoms, a critically important class of phytoplankton in terms of carbon export production. This is achieved in part by including iron, on which phytoplankton uptake of silicic acid depends. Also, MESMO 2 is coupled to an existing terrestrial model, which allows for the exchange of carbon, water, and energy between land and the atmosphere. The coupled model, called MESMO 2E, is appropriate for more complete earth system simulations. The new version was calibrated with the goal of preserving reasonable interior ocean ventilation and various biological production rates in the ocean and land, while simulating key features of the marine silica cycle.
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Brault, M. O., L. A. Mysak, and H. D. Matthews. "Carbon cycle implications of terrestrial weathering changes since the last glacial maximum." FACETS 2, no. 1 (May 1, 2017): 267–85. http://dx.doi.org/10.1139/facets-2016-0040.
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We examine the importance of the rock weathering feedback mechanism during the last deglacial period (∼16 000–4000 BCE) using an Earth system model of intermediate complexity (the University of Victoria Earth System Climate Model (UVic ESCM)) with four box-model parameterizations of terrestrial weathering. The deglacial climate change is driven by changes in orbital parameters, ice core reconstructions of atmospheric CO2 variability, and prescribed removal of continental ice sheets. Over the course of the 12 000 year simulation period, increases in weathering provide a mechanism that slowly removes CO2 from the atmosphere, in opposition to the observed atmospheric CO2 increase during this period. These processes transfer both carbon and alkalinity to the ocean, the combination of which results in as much as a 1000 Pg C increase in total ocean carbon, relative to a control simulation with constant weathering. However, the rapid expansion of northern hemisphere vegetation introduces a significant uncertainty among the weathering parameterizations. Further experiments to test the individual impacts of weathering dissolved inorganic carbon and alkalinity fluxes on ocean biogeochemistry suggest that the worldwide distribution of rock types and the ratio of carbonate to silicate weathering may be crucially important in obtaining an accurate estimate of changes in global weathering rates.
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Pinto Junior, Osvaldo Borges, Paula Valéria Carvalho, and Eduardo Guimarães Couto. "Study of CO2 flux and soil carbon in northern Pantanal, Brazil." Revista Ibero-Americana de Ciências Ambientais 9, no. 5 (September 24, 2018): 29–38. http://dx.doi.org/10.6008/cbpc2179-6858.2018.005.0004.
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The determination of greenhouse gas emissions from wetlands are of great interest given the biogeochemistry these areas exhibit. We measure soil CO2 concentration and monthly fluxes on a tree island of the Northern Pantanal of Mato Grosso, Brazil, and estimate the role of soil as a carbon source or sink during high tide, low tide, flooding, and drought seasons. The average value of the CO2 fluxes in the wetland soil was 0.54 ± 0.30 g (CO2)·m- 2·h- 1 with the soil acting as a carbon source at -9.11 ton.·ha-1 over the one year cycle. Soil CO2 fluxes were significantly correlated with soil moisture and temperature at 5 cm depth. Soil CO2 concentrations reached more than 100 ppm. Soil carbon stocks did not correlate significantly with variables in this study, suggesting that non-measured variables can influence soil carbon dynamics.
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Arnosti, C., M. Wietz, T. Brinkhoff, J. H. Hehemann, D. Probandt, L. Zeugner, and R. Amann. "The Biogeochemistry of Marine Polysaccharides: Sources, Inventories, and Bacterial Drivers of the Carbohydrate Cycle." Annual Review of Marine Science 13, no. 1 (January 3, 2021): 81–108. http://dx.doi.org/10.1146/annurev-marine-032020-012810.
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Polysaccharides are major components of macroalgal and phytoplankton biomass and constitute a large fraction of the organic matter produced and degraded in the ocean. Until recently, however, our knowledge of marine polysaccharides was limited due to their great structural complexity, the correspondingly complicated enzymatic machinery used by microbial communities to degrade them, and a lack of readily applied means to isolate andcharacterize polysaccharides in detail. Advances in carbohydrate chemistry, bioinformatics, molecular ecology, and microbiology have led to new insights into the structures of polysaccharides, the means by which they are degraded by bacteria, and the ecology of polysaccharide production and decomposition. Here, we survey current knowledge, discuss recent advances, and present a new conceptual model linking polysaccharide structural complexity and abundance to microbially driven mechanisms of polysaccharide processing. We conclude by highlighting specific future research foci that will shed light on this central but poorly characterized component of the marine carbon cycle.
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Dall'Olmo, G., E. Boss, M. J. Behrenfeld, T. K. Westberry, C. Courties, L. Prieur, M. Pujo-Pay, N. Hardman-Mountford, and T. Moutin. "Inferring phytoplankton carbon and eco-physiological rates from diel cycles of spectral particulate beam-attenuation coefficient." Biogeosciences 8, no. 11 (November 28, 2011): 3423–39. http://dx.doi.org/10.5194/bg-8-3423-2011.
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Abstract. The diurnal fluctuations in solar irradiance impose a fundamental frequency on ocean biogeochemistry. Observations of the ocean carbon cycle at these frequencies are rare, but could be considerably expanded by measuring and interpreting the inherent optical properties. A method is presented to analyze diel cycles in particulate beam-attenuation coefficient (cp) measured at multiple wavelengths. The method is based on fitting observations with a size-structured population model coupled to an optical model to infer the particle size distribution and physiologically relevant parameters of the cells responsible for the measured diel cycle in cp. Results show that the information related to size and contained in the spectral data can be exploited to independently estimate growth and loss rates during the day and night. In addition, the model can characterize the population of particles affecting the diel variability in cp. Application of this method to spectral cp measured at a station in the oligotrophic Mediterranean Sea suggests that most of the observed variations in cp can be ascribed to a synchronized population of cells with an equivalent spherical diameter around 4.6±1.5 μm. The inferred carbon biomass of these cells was about 5.2–6.0 mg m−3 and accounted for approximately 10% of the total particulate organic carbon. If successfully validated, this method may improve our in situ estimates of primary productivity.
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Fang, Y., C. Liu, and L. R. Leung. "Accelerating the spin-up of the coupled carbon and nitrogen cycle model in CLM4." Geoscientific Model Development Discussions 7, no. 6 (December 20, 2014): 9109–32. http://dx.doi.org/10.5194/gmdd-7-9109-2014.
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Abstract. The commonly adopted biogeochemistry spin-up process in earth system model is to run the model for hundreds to thousands of years subject to periodic atmospheric forcing to reach dynamic steady state of the carbon-nitrogen (CN) models. A variety of approaches have been proposed to reduce the computation time of the spin-up process. Significant improvement in computational efficiency has been made recently. However, a long simulation time is still required to reach the common convergence criteria of the coupled carbon/nitrogen model. A gradient projection method was proposed and used to further reduce the computation time after examining the trend of the dominant carbon pools. The Community Land Model version 4 (CLM4) with carbon and nitrogen component was used in this study. From point scale simulations we found that the method can reduce the computation time by 20–69% compared to the fastest approach in the literature. We also found that the cyclic stability of total carbon for some cases differs from that of the periodic atmospheric forcing, and some cases even showed instability. Close examination showed that one case has a carbon periodicity much longer than that of the atmospheric forcing due to the annual fire disturbance that is longer than half a year. The rest was caused by the instability of water table calculation in the hydrology model of CLM4. The instability issue is resolved after we replaced the hydrology scheme in CLM4 with a low model for variably saturated porous media.
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Zhang, ChuanLun. "Untangling the role that microbes play in ocean carbon cycle─A new paradigm in marine biogeochemistry." Science China Earth Sciences 60, no. 2 (December 23, 2016): 409–12. http://dx.doi.org/10.1007/s11430-016-0217-x.
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Beaupré, Steven R., David J. Kieber, William C. Keene, Michael S. Long, John R. Maben, Xi Lu, Yuting Zhu, et al. "Oceanic efflux of ancient marine dissolved organic carbon in primary marine aerosol." Science Advances 5, no. 10 (October 2019): eaax6535. http://dx.doi.org/10.1126/sciadv.aax6535.
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Breaking waves produce bubble plumes that burst at the sea surface, injecting primary marine aerosol (PMA) highly enriched with marine organic carbon (OC) into the atmosphere. It is widely assumed that this OC is modern, produced by present-day biological activity, even though nearly all marine OC is thousands of years old, produced by biological activity long ago. We used natural abundance radiocarbon (14C) measurements to show that 19 to 40% of the OC associated with freshly produced PMA was refractory dissolved OC (RDOC). Globally, this process removes 2 to 20 Tg of RDOC from the oceans annually, comparable to other RDOC losses. This process represents a major removal pathway for old OC from the sea, with important implications for oceanic and atmospheric biogeochemistry, the global carbon cycle, and climate.
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Matsumoto, George I., Kenneth S. Johnson, Steve Riser, Lynne Talley, Susan Wijffels, and Roberta Hotinski. "The Global Ocean Biogeochemistry (GO-BGC) Array of Profiling Floats to Observe Changing Ocean Chemistry and Biology." Marine Technology Society Journal 56, no. 3 (June 8, 2022): 122–23. http://dx.doi.org/10.4031/mtsj.56.3.25.
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Abstract The Global Ocean Biogeochemistry (GO-BGC) Array is a project funded by the US National Science Foundation to build a global network of chemical and biological sensors on Argo profiling floats. The network will monitor biogeochemical cycles and ocean health. The floats will collect from a depth of 2,000 meters to the surface, augmenting the existing <ext-link ext-link-type="uri" xlink:href="https://argo.ucsd.edu/">Argo array</ext-link> that monitors ocean temperature and salinity. Data will be made freely available within a day of being collected via the Argo data system. These data will allow scientists to pursue fundamental questions concerning ocean ecosystems, monitor ocean health and productivity, and observe the elemental cycles of carbon, oxygen, and nitrogen through all seasons of the year. Such essential data are needed to improve computer models of ocean fisheries and climate, to monitor and forecast the effects of ocean warming and ocean acidification on sea life, and to address key questions identified in “Sea Change: 2015‐2025 Decadal Survey of Ocean Sciences” such as: What is the ocean's role in regulating the carbon cycle? What are the natural and anthropogenic drivers of open ocean deoxygenation? What are the consequences of ocean acidification? How do physical changes in mixing and circulation affect nutrient availability and ocean productivity?
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Zhang, Chuanlun, Hongyue Dang, Farooq Azam, Ronald Benner, Louis Legendre, Uta Passow, Luca Polimene, Carol Robinson, Curtis A. Suttle, and Nianzhi Jiao. "Evolving paradigms in biological carbon cycling in the ocean." National Science Review 5, no. 4 (July 1, 2018): 481–99. http://dx.doi.org/10.1093/nsr/nwy074.
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ABSTRACT Carbon is a keystone element in global biogeochemical cycles. It plays a fundamental role in biotic and abiotic processes in the ocean, which intertwine to mediate the chemistry and redox status of carbon in the ocean and the atmosphere. The interactions between abiotic and biogenic carbon (e.g. CO2, CaCO3, organic matter) in the ocean are complex, and there is a half-century-old enigma about the existence of a huge reservoir of recalcitrant dissolved organic carbon (RDOC) that equates to the magnitude of the pool of atmospheric CO2. The concepts of the biological carbon pump (BCP) and the microbial loop (ML) shaped our understanding of the marine carbon cycle. The more recent concept of the microbial carbon pump (MCP), which is closely connected to those of the BCP and the ML, explicitly considers the significance of the ocean's RDOC reservoir and provides a mechanistic framework for the exploration of its formation and persistence. Understanding of the MCP has benefited from advanced ‘omics’ and novel research in biological oceanography and microbial biogeochemistry. The need to predict the ocean's response to climate change makes an integrative understanding of the BCP, ML and MCP a high priority. In this review, we summarize and discuss progress since the proposal of the MCP in 2010 and formulate research questions for the future.
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Willeit, Matteo, Tatiana Ilyina, Bo Liu, Christoph Heinze, Mahé Perrette, Malte Heinemann, Daniela Dalmonech, et al. "The Earth system model CLIMBER-X v1.0 – Part 2: The global carbon cycle." Geoscientific Model Development 16, no. 12 (June 27, 2023): 3501–34. http://dx.doi.org/10.5194/gmd-16-3501-2023.
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Abstract. The carbon cycle component of the newly developed Earth system model of intermediate complexity CLIMBER-X is presented. The model represents the cycling of carbon through the atmosphere, vegetation, soils, seawater and marine sediments. Exchanges of carbon with geological reservoirs occur through sediment burial, rock weathering and volcanic degassing. The state-of-the-art HAMOCC6 model is employed to simulate ocean biogeochemistry and marine sediment processes. The land model PALADYN simulates the processes related to vegetation and soil carbon dynamics, including permafrost and peatlands. The dust cycle in the model allows for an interactive determination of the input of the micro-nutrient iron into the ocean. A rock weathering scheme is implemented in the model, with the weathering rate depending on lithology, runoff and soil temperature. CLIMBER-X includes a simple representation of the methane cycle, with explicitly modelled natural emissions from land and the assumption of a constant residence time of CH4 in the atmosphere. Carbon isotopes 13C and 14C are tracked through all model compartments and provide a useful diagnostic for model–data comparison. A comprehensive evaluation of the model performance for the present day and the historical period shows that CLIMBER-X is capable of realistically reproducing the historical evolution of atmospheric CO2 and CH4 but also the spatial distribution of carbon on land and the 3D structure of biogeochemical ocean tracers. The analysis of model performance is complemented by an assessment of carbon cycle feedbacks and model sensitivities compared to state-of-the-art Coupled Model Intercomparison Project Phase 6 (CMIP6) models. Enabling an interactive carbon cycle in CLIMBER-X results in a relatively minor slow-down of model computational performance by ∼ 20 % compared to a throughput of ∼ 10 000 simulation years per day on a single node with 16 CPUs on a high-performance computer in a climate-only model set-up. CLIMBER-X is therefore well suited to investigating the feedbacks between climate and the carbon cycle on temporal scales ranging from decades to >100 000 years.
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Chien, Chia-Te, Jonathan V. Durgadoo, Dana Ehlert, Ivy Frenger, David P. Keller, Wolfgang Koeve, Iris Kriest, et al. "FOCI-MOPS v1 – integration of marine biogeochemistry within the Flexible Ocean and Climate Infrastructure version 1 (FOCI 1) Earth system model." Geoscientific Model Development 15, no. 15 (August 2, 2022): 5987–6024. http://dx.doi.org/10.5194/gmd-15-5987-2022.
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Abstract. The consideration of marine biogeochemistry is essential for simulating the carbon cycle in an Earth system model. Here we present the implementation and evaluation of a marine biogeochemical model, the Model of Oceanic Pelagic Stoichiometry (MOPS) in the Flexible Ocean and Climate Infrastructure (FOCI) climate model. FOCI-MOPS enables the simulation of marine biological processes, i.e. the marine carbon, nitrogen, and oxygen cycles with prescribed or prognostic atmospheric CO2 concentration. A series of experiments covering the historical period (1850–2014) were performed following the DECK (Diagnostic, Evaluation and Characterization of Klima) and CMIP6 (Coupled Model Intercomparison Project 6) protocols. Overall, modelled biogeochemical tracer distributions and fluxes, transient evolution in surface air temperature, air–sea CO2 fluxes, and changes in ocean carbon and heat contents are in good agreement with observations. Modelled inorganic and organic tracer distributions are quantitatively evaluated by statistically derived metrics. Results of the FOCI-MOPS model, including sea surface temperature, surface pH, oxygen (100–600 m), nitrate (0–100 m), and primary production, are within the range of other CMIP6 model results. Overall, the evaluation of FOCI-MOPS indicates its suitability for Earth climate system simulations.
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Fang, Y., C. Liu, and L. R. Leung. "Accelerating the spin-up of the coupled carbon and nitrogen cycle model in CLM4." Geoscientific Model Development 8, no. 3 (March 24, 2015): 781–89. http://dx.doi.org/10.5194/gmd-8-781-2015.
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Abstract. The commonly adopted biogeochemistry spin-up process in an Earth system model (ESM) is to run the model for hundreds to thousands of years subject to periodic atmospheric forcing to reach dynamic steady state of the carbon–nitrogen (CN) models. A variety of approaches have been proposed to reduce the computation time of the spin-up process. Significant improvement in computational efficiency has been made recently. However, a long simulation time is still required to reach the common convergence criteria of the coupled carbon–nitrogen model. A gradient projection method was proposed and used to further reduce the computation time after examining the trend of the dominant carbon pools. The Community Land Model version 4 (CLM4) with a carbon and nitrogen component was used in this study. From point-scale simulations, we found that the method can reduce the computation time by 20–69% compared to one of the fastest approaches in the literature. We also found that the cyclic stability of total carbon for some cases differs from that of the periodic atmospheric forcing, and some cases even showed instability. Close examination showed that one case has a carbon periodicity much longer than that of the atmospheric forcing due to the annual fire disturbance that is longer than half a year. The rest was caused by the instability of water table calculation in the hydrology model of CLM4. The instability issue is resolved after we replaced the hydrology scheme in CLM4 with a flow model for variably saturated porous media.
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Matsumoto, K., K. S. Tokos, A. R. Price, and S. J. Cox. "First description of the Minnesota Earth System Model for Ocean biogeochemistry (MESMO 1.0)." Geoscientific Model Development 1, no. 1 (August 4, 2008): 1–15. http://dx.doi.org/10.5194/gmd-1-1-2008.
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Abstract. Here we describe the first version of the Minnesota Earth System Model for Ocean biogeochemistry (MESMO 1.0), an intermediate complexity model based on the Grid ENabled Integrated Earth system model (GENIE-1). As with GENIE-1, MESMO has a 3D dynamical ocean, energy-moisture balance atmosphere, dynamic and thermodynamic sea ice, and marine biogeochemistry. Main development goals of MESMO were to: (1) bring oceanic uptake of anthropogenic transient tracers within data constraints; (2) increase vertical resolution in the upper ocean to better represent near-surface biogeochemical processes; (3) calibrate the deep ocean ventilation with observed abundance of radiocarbon. We achieved all these goals through a combination of objective model optimization and subjective targeted tuning. An important new feature in MESMO that dramatically improved the uptake of CFC-11 and anthropogenic carbon is the depth dependent vertical diffusivity in the ocean, which is spatially uniform in GENIE-1. In MESMO, biological production occurs in the top two layers above the compensation depth of 100 m and is modified by additional parameters, for example, diagnosed mixed layer depth. In contrast, production in GENIE-1 occurs in a single layer with thickness of 175 m. These improvements make MESMO a well-calibrated model of intermediate complexity suitable for investigations of the global marine carbon cycle requiring long integration time.
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Leloup, Gaëlle, та Didier Paillard. "Multi-million-year cycles in modelled δ13C as a response to astronomical forcing of organic matter fluxes". Earth System Dynamics 14, № 2 (21 березня 2023): 291–307. http://dx.doi.org/10.5194/esd-14-291-2023.
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Abstract. Along with 400 kyr periodicities, multi-million-year cycles have been found in δ13C records over different time periods. An ∼ 8–9 Myr periodicity is found throughout the Cenozoic and part of the Mesozoic. The robust presence of this periodicity in δ13C records suggests an astronomical origin. However, this periodicity is barely visible in the astronomical forcing. Due to the large fractionation factor of organic matter, its burial or oxidation produces large δ13C variations for moderate carbon variations. Therefore, astronomical forcing of organic matter fluxes is a plausible candidate to explain the oscillations observed in the δ13C records. So far, modelling studies forcing astronomically the organic matter burial have been able to produce 400 kyr and 2.4 Myr cycles in δ13C but were not able to produce longer cycles, such as 8–9 Myr cycles. Here, we propose a mathematical mechanism compatible with the biogeochemistry that could explain the presence of multi-million-year cycles in the δ13C records and their stability over time: a preferential phase locking to multiples of the 2.4 Myr eccentricity period. With a simple non-linear conceptual model for the carbon cycle that has multiple equilibria, we are able to extract longer periods than with a simple linear model – more specifically, multi-million-year periods.
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Nickelsen, L., D. P. Keller, and A. Oschlies. "A dynamic marine iron cycle module coupled to the University of Victoria Earth System Model: the Kiel Marine Biogeochemical Model 2 (KMBM2) for UVic 2.9." Geoscientific Model Development Discussions 7, no. 6 (December 5, 2014): 8505–63. http://dx.doi.org/10.5194/gmdd-7-8505-2014.
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Abstract. Marine biological production and the associated biotic uptake of carbon in many ocean regions depend on the availability of nutrients in the euphotic zone. While large areas are limited by nitrogen and/or phosphorus, the micronutrient iron is considered the main limiting nutrient in the North Pacific, equatorial Pacific and Southern Ocean. Changes in iron availability via changes in atmospheric dust input are discussed to play an important role in glacial/interglacial cycles via climate feedbacks caused by changes in biological ocean carbon sequestration. Although many aspects of the iron cycle remain unknown, its incorporation into marine biogeochemical models is needed to test our current understanding and better constrain its role in the Earth system. In the University of Victoria Earth System Climate Model (UVic) iron limitation in the ocean was, until now, simulated pragmatically with an iron concentration masking scheme that did not allow a consistent interactive response to perturbations of ocean biogeochemistry or iron cycling sensitivity studies. Here, we replace the iron masking scheme with a dynamic iron cycle and compare the results to available observations and the previous marine biogeochemical model. Sensitivity studies are also conducted with the new model to test the importance of considering the variable solubility of iron in dust deposition, the importance of considering high resolution bathymetry for the sediment release of iron, the effect of scaling the sedimentary iron release with temperature and the sensitivity of the iron cycle to a climate change scenario.
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Burke, Eleanor, Sarah Chadburn, and Chris Huntingford. "Thawing Permafrost as a Nitrogen Fertiliser: Implications for Climate Feedbacks." Nitrogen 3, no. 2 (June 3, 2022): 353–75. http://dx.doi.org/10.3390/nitrogen3020023.
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Studies for the northern high latitudes suggest that, in the near term, increased vegetation uptake may offset permafrost carbon losses, but over longer time periods, permafrost carbon decomposition causes a net loss of carbon. Here, we assess the impact of a coupled carbon and nitrogen cycle on the simulations of these carbon fluxes. We present results from JULES-IMOGEN—a global land surface model coupled to an intermediate complexity climate model with vertically resolved soil biogeochemistry. We quantify the impact of nitrogen fertilisation from thawing permafrost on the carbon cycle and compare it with the loss of permafrost carbon. Projections show that the additional fertilisation reduces the high latitude vegetation nitrogen limitation and causes an overall increase in vegetation carbon uptake. This is a few Petagrams of carbon (Pg C) by year 2100, increasing to up to 40 Pg C by year 2300 for the RCP8.5 concentration scenario and adds around 50% to the projected overall increase in vegetation carbon in that region. This nitrogen fertilisation results in a negative (stabilising) feedback on the global mean temperature, which could be equivalent in magnitude to the positive (destabilising) temperature feedback from the loss of permafrost carbon. This balance depends on the future scenario and initial permafrost carbon. JULES-IMOGEN describes one representation of the changes in Arctic carbon and nitrogen cycling in response to climate change. However there are uncertainties in the modelling framework, model parameterisation and missing processes which, when assessed, will provide a more complete picture of the balance between stabilising and destabilising feedbacks.
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Buesseler, Ken. "Ocean Biogeochemistry and the Global Carbon Cycle: An Introduction to the U.S. Joint Global Ocean Flux Study." Oceanography 14, no. 4 (2001): 5. http://dx.doi.org/10.5670/oceanog.2001.01.
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Moutin, T., F. Van Wambeke, and L. Prieur. "Introduction to the Biogeochemistry from the Oligotrophic to the Ultraoligotrophic Mediterranean (BOUM) experiment." Biogeosciences 9, no. 10 (October 8, 2012): 3817–25. http://dx.doi.org/10.5194/bg-9-3817-2012.
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Abstract. The overall goal of the BOUM (Biogeochemistry from the Oligotrophic to the Ultraoligotrophic Mediterranean) experiment was to obtain a better representation of the interactions between planktonic organisms and the cycle of biogenic elements in the Mediterranean Sea (MS), in the context of global climate change and, more particularly, on the role of the ocean in carbon sequestration through biological processes. The BOUM experiment was organized around three main objectives: (1) to give a longitudinal description of the biogeochemistry and the biological diversity of the MS during the strongest stratified period, (2) to study processes at the centre of three anticyclonic eddies, and (3) to obtain a representation of the main biogeochemical fluxes and the dynamics of the planktonic trophic network. The international BOUM cruise took place between 16 June and 20 July 2008, involved 32 scientists on board, and covered around 3000 km in the MS from the south of Cyprus to Marseilles (France). This paper describes in detail the objectives of the BOUM experiment, the implementation plan of the cruise before giving an introduction of the 25 other papers published in this special issue.
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Doney, Scott C., Keith Lindsay, Inez Fung, and Jasmin John. "Natural Variability in a Stable, 1000-Yr Global Coupled Climate–Carbon Cycle Simulation." Journal of Climate 19, no. 13 (July 1, 2006): 3033–54. http://dx.doi.org/10.1175/jcli3783.1.
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Abstract A new 3D global coupled carbon–climate model is presented in the framework of the Community Climate System Model (CSM-1.4). The biogeochemical module includes explicit land water–carbon coupling, dynamic carbon allocation to leaf, root, and wood, prognostic leaf phenology, multiple soil and detrital carbon pools, oceanic iron limitation, a full ocean iron cycle, and 3D atmospheric CO2 transport. A sequential spinup strategy is utilized to minimize the coupling shock and drifts in land and ocean carbon inventories. A stable, 1000-yr control simulation [global annual mean surface temperature ±0.10 K and atmospheric CO2 ± 1.2 ppm (1σ)] is presented with no flux adjustment in either physics or biogeochemistry. The control simulation compares reasonably well against observations for key annual mean and seasonal carbon cycle metrics; regional biases in coupled model physics, however, propagate clearly into biogeochemical error patterns. Simulated interannual-to-centennial variability in atmospheric CO2 is dominated by terrestrial carbon flux variability, ±0.69 Pg C yr−1 (1σ global net annual mean), which in turn reflects primarily regional changes in net primary production modulated by moisture stress. Power spectra of global CO2 fluxes are white on time scales beyond a few years, and thus most of the variance is concentrated at high frequencies (time scale &lt;4 yr). Model variability in air–sea CO2 fluxes, ±0.10 Pg C yr−1 (1σ global annual mean), is generated by variability in sea surface temperature, wind speed, export production, and mixing/upwelling. At low frequencies (time scale &gt;20 yr), global net ocean CO2 flux is strongly anticorrelated (0.7–0.95) with the net CO2 flux from land; the ocean tends to damp (20%–25%) slow variations in atmospheric CO2 generated by the terrestrial biosphere. The intrinsic, unforced natural variability in land and ocean carbon storage is the “noise” that complicates the detection and mechanistic attribution of contemporary anthropogenic carbon sinks.
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Brovkin, V., A. Ganopolski, D. Archer, and G. Munhoven. "Glacial CO<sub>2</sub> cycle as a succession of key physical and biogeochemical processes." Climate of the Past 8, no. 1 (February 9, 2012): 251–64. http://dx.doi.org/10.5194/cp-8-251-2012.
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Abstract. During glacial-interglacial cycles, atmospheric CO2 concentration varied by about 100 ppmv in amplitude. While testing mechanisms that have led to the low glacial CO2 level could be done in equilibrium model experiments, an ultimate goal is to explain CO2 changes in transient simulations through the complete glacial-interglacial cycle. The computationally efficient Earth System model of intermediate complexity CLIMBER-2 is used to simulate global biogeochemistry over the last glacial cycle (126 kyr). The physical core of the model (atmosphere, ocean, land and ice sheets) is driven by orbital changes and reconstructed radiative forcing from greenhouses gases, ice, and aeolian dust. The carbon cycle model is able to reproduce the main features of the CO2 changes: a 50 ppmv CO2 drop during glacial inception, a minimum concentration at the last glacial maximum 80 ppmv lower than the Holocene value, and an abrupt 60 ppmv CO2 rise during the deglaciation. The model deep ocean δ13C also resembles reconstructions from deep-sea cores. The main drivers of atmospheric CO2 evolve in time: changes in sea surface temperatures and in the volume of bottom water of southern origin control atmospheric CO2 during the glacial inception and deglaciation; changes in carbonate chemistry and marine biology are dominant during the first and second parts of the glacial cycle, respectively. These feedback mechanisms could also significantly impact the ultimate climate response to the anthropogenic perturbation.