ALBERT

Description: Phosphorus (P) plays a vital role in global crop production and food security. In this study, we investigate the changes in soil P pools and crop P uptake, using a 0.5 by 0.5 degree spatially explicit model for the period 1900–2010. The simulated country-scale crop P uptake agrees well with historical P uptake. Simulated crop P uptake is influenced by both soil properties (available P and the P retention potential) and crop characteristics (maximum uptake). Until 1950, P fertilizer application had a negligible influence on crop uptake, but recently it has become a driving factor for food production in industrialized countries and a number of transition countries like Brazil, Korea and China. Globally, the total P pool per hectare increased rapidly between 1900 and 2010 in soils of Europe (+31 %), South America (+2 %), North America (+15 %), Asia (+17 %) and Oceania (+17 %), while it has been stable in Africa. This comprehensive and spatially explicit model can be used to assess the dynamics of soil P inventories, which serve as indicators for soil fertility and productivity.

Description: Phosphorus (P) plays a vital role in global crop production and food security. In this study, we investigate the changes in soil P pool inventories calibrated from historical countrywide crop P uptake, using a 0.5-by-0.5° spatially explicit model for the period 1900–2010. Globally, the total P pool per hectare increased rapidly between 1900 and 2010 in soils of Europe (+31 %), South America (+2 %), North America (+15 %), Asia (+17 %), and Oceania (+17 %), while it has been stable in Africa. Simulated crop P uptake is influenced by both soil properties (available P and the P retention potential) and crop characteristics (maximum uptake). Until 1950, P fertilizer application had a negligible influence on crop uptake, but recently it has become a driving factor for food production in industrialized countries and a number of transition countries like Brazil, Korea, and China. This comprehensive and spatially explicit model can be used to assess how long surplus P fertilization is needed or how long depletions of built-up surplus P can continue without affecting crop yield.

Description: Here, we present the implementation of the freshwater carbon (C) cycle in the Dynamic In-stream Chemistry module (CARBON-DISC), which is part of the Integrated Model to Assess the Global Environment-Dynamic Global Nutrient Model (IMAGE-DGNM). A coupled hydrology-biogeochemistry approach with 0.5 by 0.5-degree resolution accounts for the spatial and temporal variability in dynamic conditions in the aquatic continuum using independent global databases. This process-based model resolves the concentrations, transformations and transfer fluxes of dissolved inorganic carbon (DIC), dissolved organic carbon (DOC) and terrestrial and autochthonous particulate organic carbon (POC) from headwaters to river mouth with a time step of 1 month for the period 1950–2000. This is a major step forward in basin scale modelling of the C processing in freshwater systems, since simulated results can be validated at every location and point in time, and the model can be applied for retrodiction and to analyse future scenarios. Validation of the model with long-term measurement data shows a fair agreement, considering that this is a global model. To analyse the performance of the full production-respiration DISC module, two other schemes are presented, including an abiotic system excluding any in-stream processing of DOC and allochthonous production, and an extended abiotic system including heterotrophic respiration, but excluding production. Furthermore, a sensitivity analysis shows that many parameters, such as temperature, solar radiation, organic sediment mineralization rate and C inputs, including particulate organic carbon from terrestrial vegetation and dissolved inorganic carbon from groundwater, strongly affect atmosphere-freshwater exchange of CO2.

Description: Various human activities – including agriculture, water consumption, river damming, and aquaculture – have intensified over the last century. This has had a major impact on nitrogen (N) and phosphorus (P) cycling in global continental waters. In this study, we use a coupled nutrient-input–hydrology–in-stream nutrient retention model to quantitatively track the changes in the global freshwater N and P cycles over the 20th century. Our results suggest that, during this period, the global nutrient delivery to streams increased from 34 to 64 Tg N yr−1 and from 5 to 9 Tg P yr−1. Furthermore, in-stream retention and removal grew from 14 to 27 Tg N yr−1 and 3 to 5 Tg P yr−1. One of the major causes of increased retention is the growing number of reservoirs, which now account for 24 and 22 % of global N and P retention/removal in freshwater systems, respectively. This increase in nutrient retention could not balance the increase in nutrient delivery to rivers with the consequence that river nutrient transport to the ocean increased from 19 to 37 Tg N yr−1 and from 2 to 4 Tg P yr−1. Human activities have also led to a global increase in the molar N : P ratio in freshwater bodies.

Description: Dissolved carbon leaching in and from soils plays an important role in C transport along the terrestrial-aquatic continuum. However, a global overview and analysis of dissolved carbon in soil solutions, covering a wide range of vegetation types and climates, is lacking. We compiled a global database on annual average dissolved organic carbon (DOC) and dissolved inorganic carbon (DIC) in soil solutions, including potential governing factors, with 762 entries from 351 different sites covering a range of climate zones, land cover types and soil classes. Using this database we develop regression models to calculate topsoil concentrations, and concentrations vs. depth in the subsoil at the global scale. For DIC, the lack of a proportional globally distributed cover inhibits analysis on a global scale. For DOC, annual average concentrations range from 1.7 to 88.3 (median = 25.27) mg C/L for topsoils and from 0.42 to 372.1 (median = 5.50) mg C/L for subsoils (excluding lab incubations). Highest topsoil values occur in forests of cooler, humid zones. In topsoils, multiple regression showed that precipitation is the most significant factor. Our global topsoil DOC model (R2 = 0.36) uses precipitation, soil class, climate zone and land cover type as model factors. Our global subsoil model describes DOC concentrations vs. depth for different USDA soil classes (overall R2 = 0.45). Highest subsoil concentrations are calculated for Histosols.

Description: The manganese nodule belt within the Clarion and Clipperton Fracture Zones (CCZ) in the abyssal NE Pacific Ocean is characterized by numerous seamounts, low organic matter (OM) depositional fluxes and meter-scale oxygen penetration depths (OPD) into the sediment. The region hosts contract areas for the exploration of polymetallic nodules and Areas of Particular Environmental Interest (APEI) as protected areas. In order to assess the impact of potential mining on these deep-sea sediments and ecosystems, a thorough determination of the natural spatial variability of depositional and geochemical conditions as well as biogeochemical processes and element fluxes in the different exploration areas is required. Here, we present a comparative study on (1) sedimentation rates and bioturbation depths, (2) redox zonation of the sediments and element fluxes as well as (3) rates and pathways of biogeochemical reactions at six sites in the eastern CCZ. The sites are located in four European contract areas and in the APEI3. Our results demonstrate that the natural spatial variability of depositional and (bio)geochemical conditions in this deep-sea sedimentary environment is much larger than previously thought. We found that the OPD varies between 1 and 4.5 m, while the sediments at two sites are oxic throughout the sampled interval (7.5 m depth). Below the OPD, manganese and nitrate reduction occur concurrently in the suboxic zone with pore-water Mn2+ concentrations of up to 25 µM. The thickness of the suboxic zone extends over depth intervals of less than 3 m to more than 8 m. Our data and the applied transport-reaction model suggest that the extension of the oxic and suboxic zones is ultimately determined by the (1) low flux of particulate organic carbon (POC) of 1–2 mg Corg m−2 d−1 to the seafloor, (2) low sedimentation rates between 0.2 and 1.15 cm kyr−1 and (3) oxidation of pore-water Mn2+ at depth. The diagenetic model reveals that aerobic respiration is the main biogeochemical process driving OM degradation. Due to very low POC fluxes of 1 mg m−2 d−1 to the seafloor at the site investigated in the protected APEI3 area, respiration rates are twofold lower than at the other study sites. Thus, the APEI3 site does not represent the (bio)geochemical conditions that prevail in the other investigated sites located in the European contract areas. Lateral variations in surface water productivity are generally reflected in the POC fluxes to the seafloor across the various areas but deviate from this trend at two of the study sites. We suggest that the observed spatial variations in depositional and (bio)geochemical conditions result from differences in the degree of degradation of OM in the water column and heterogeneous sedimentation patterns caused by the interaction of bottom water currents with seafloor topography.

Description: Manganese nodules of the Clarion–Clipperton Fracture Zone (CCFZ) in the NE Pacific Ocean are highly enriched in Ni, Cu, Co, Mo and rare-earth elements, and thus may be the subject of future mining operations. Elucidating the depositional and biogeochemical processes that contribute to nodule formation, as well as the respective redox environment, in both water column and sediment, supports our ability to locate future nodule deposits and to evaluate the potential ecological and environmental effects of future deep-sea mining. For these purposes we studied the local hydrodynamics and pore-water geochemistry with respect to the nodule coverage at four sites in the eastern CCFZ. Furthermore, we carried out selective leaching experiments at these sites in order to assess the potential mobility of Mn in the solid phase, and compared them with the spatial variations in sedimentation rates. We found that the oxygen penetration depth is 180–300 cm at all four sites, while reduction of Mn and NO3− is only significant below the oxygen penetration depth at sites with small or no nodules on the sediment surface. At the site without nodules, potential microbial respiration rates, determined by incubation experiments using 14C-labeled acetate, are slightly higher than at sites with nodules. Leaching experiments showed that surface sediments covered with big or medium-sized nodules are enriched in mobilizable Mn. Our deep oxygen measurements and pore-water data suggest that hydrogenetic and oxic-diagenetic processes control the present-day nodule growth at these sites, since free manganese from deeper sediments is unable to reach the sediment surface. We propose that the observed strong lateral contrasts in nodule size and abundance are sensitive to sedimentation rates, which in turn, are controlled by small-scale variations in seafloor topography and bottom-water current intensity.