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Mesocosm experiment on the influence of heatwave on plankton

In the context of global change, marine organisms are subjected not only to gradual changes in abiotic parameters, but also to an increasing number of extreme events, such as heatwaves. However, we still know little about the influence of heatwaves on the structure of marine communities, and experimental studies are needed to test the impact of heatwaves alone, and in combination with other environmental drivers. Here, we conducted a mesocosm experiment and applied an integrated multiple driver design to assess the potential impact of heatwaves under ambient and future environmental conditions on natural coastal plankton communities. To represent future environmental conditions, temperature and pH were manipulated based on the Representative Concentration Pathway 8.5 proposed by the IPCC for 2100, and dissolved N:P ratios were increased to simulate the conditions expected in European coastal zones. Throughout the experiment, we measured abiotic conditions as well as the abundance of bacterioplankton, phytoplankton, and microzooplankton.

KOSMOS 2023 Helgoland mesocosm study on ocean alkalinity enhancement: sediment trap particle flux data and water column biogeochemistry

The data presented herein originates from a mesocosm study conducted as part of the BMBF CDRmare, Retake project (grant agreement no. 03F0895A), aimed at investigating the ecological ramifications of ocean alkalinity enhancement (OAE). Twelve mesocosms were deployed in Helgoland South Harbor, Germany, and systematically sampled using integrated water samplers over the period spanning from March 12th to April 20th, 2023. Six alkalinity levels under two dilution scenarios were established to differentiate between localized and uniform OAE additions. Alkalinity was increased stepwise to ΔTAmax = 1250 μmol kg-1 (250 μmol TA kg-1 increments) using sodium hydroxide (NaOH) with calcium chloride (CaCl2) to simulate cation release during calcium-based mineral dissolution, causing strong carbonate chemistry perturbations (e.g., pHT > 9.25). The dataset encompasses a spectrum of sediment trap particle flux data, water column biogeochemistry including pigment variables, inorganic nutrients, carbonate chemistry parameters. The study and data set offer insights into impacts of alkalinity enhancement on marine ecosystems and their associated biogeochemistry.

Natural ocean alkalinization through erosion of glacial till and weathering at the seafloor: solid phase data from AL543

Climate change-driven deglaciation and erosion in high-latitude regions enhance the flux of terrigenous material to the coastal ocean. Newly exposed land surfaces left behind by retreating glaciers are covered by glacial till, which is rich in fine-grained minerals. Many of these minerals are undersaturated in seawater and thus prone to dissolution (i.e., seafloor weathering). Consequently, intensified erosion and mineral weathering may act as an additional CO₂ sink while supplying alkalinity to coastal waters. To evaluate this hypothesis, we carried out a sediment geochemical study in the southwestern Baltic Sea, where coastal erosion of glacial till is the dominant source of terrigenous material to offshore depocenters. We analyzed glacial till from coastal cliffs, sediments, and pore waters for major element composition using inductively coupled plasma optical emission spectroscopy and an elemental analyzer. Water samples were further analyzed for dissolved redox species and dissolved silica by photometry and ion chromatography. These data were then used to quantify mineral dissolution and precipitation processes and to assess their net effect on inorganic carbon cycling.

Natural ocean alkalinization through erosion of glacial till and weathering at the seafloor: porewater data from AL543

Climate change-driven deglaciation and erosion in high-latitude regions enhance the flux of terrigenous material to the coastal ocean. Newly exposed land surfaces left behind by retreating glaciers are covered by glacial till, which is rich in fine-grained minerals. Many of these minerals are undersaturated in seawater and thus prone to dissolution (i.e., seafloor weathering). Consequently, intensified erosion and mineral weathering may act as an additional CO₂ sink while supplying alkalinity to coastal waters. To evaluate this hypothesis, we carried out a sediment geochemical study in the southwestern Baltic Sea, where coastal erosion of glacial till is the dominant source of terrigenous material to offshore depocenters. We analyzed glacial till from coastal cliffs, sediments, and pore waters for major element composition using inductively coupled plasma optical emission spectroscopy and an elemental analyzer. Water samples were further analyzed for dissolved redox species and dissolved silica by photometry and ion chromatography. These data were then used to quantify mineral dissolution and precipitation processes and to assess their net effect on inorganic carbon cycling.

An integrated multiple driver mesocosm experiment reveals the effect of global change on planktonic food web structure

We conducted a mesocosm experiment with an integrated multiple driver design to assess the impact of future global change scenarios on plankton, a key component of marine food webs. The experimental treatments were based on the RCP 6.0 and 8.5 scenarios developed by the IPCC, which were Extended (ERCP) to integrate the future predicted changing nutrient inputs into coastal waters. The mesocosm experiment was conducted over three weeks in late-summer (August-September) 2018. Seawater containing a natural plankton community was collected from the coastal North Sea. At the onset of the experiment, CO2 saturated seawater was added to the ERCP scenario mesocosms to adjust pCO2 and pH levels for each scenario. To create a realistic environment, we also manipulated the atmospheric pCO2 in the enclosed mesocosm tanks throughout the experiment. Seawater temperature was adjusted daily according to the current North Sea temperature measured at the Helgoland Roads for the Ambient, and 1.5°C and 3.0°C warmer for the ERCP 6.0 and ERCP 8.5 scenarios, respectively. Dissolved nutrient concentrations were determined at the onset of the experiment and adjusted to reach the desired N:P ratios. Samples were taken in an interval of 1-3 days depending on the phytoplankton bloom development, and community composition, except for the large mesozooplankton, was monitored throughout the experiment period.

Forschergruppe (FOR) 1525: INUIT - Ice Nuclei research UnIT, Heterogende Eisnukleation ausgelöst durch poröse Materialien

Die Nukleation von Eispartikeln spielt eine wichtige Rolle bei der Wolken- und Niederschlagsbildung, mit Konsequenten für die atmosphärische Chemie, die Wolkenphysik und das Erdklima. Für eine Quantifizierung und Vorhersage des Einflusses von Wolken in Wettervorhersage- und Klimamodellen muss die Bildung von Eispartikeln daher in einer realistischen Art und Weise beschrieben werden. Einer der wichtigen Bildungsmechanismen ist dabei die heterogene Eisnukleation im Immersionsmodus, bei dem Eis an der Oberfläche eines in einem wässrigen Tröpfchen suspendierten Eiskeims - zum Beispiel eines Mineralstaub- Partikels - gebildet wird. Wir werden im Rahmen dieses Forschungsprojekts zahlreiche Gefrierexperimente im Immersionsmodus durchführen. So werden eine Reihe verschiedener, als Aerosolpartikel in der Atmosphäre vorkommende Materialien auf ihre Eisnukleationseigenschaften hin untersucht werden. Insbesondere sollen hier die Temperatur- und Zeitabhängigkeit der von diesen Materialien ausgelösten Eisnukleation quantifiziert werden. Dabei werden wir spezielles Augenmerk auf die systematische Untersuchung der von porösen Materialien ausgelösten Eisnukleation legen. Es sollen sowohl synthetische Materialien wie beispielsweise mesoporöse Silikate untersucht werden, als auch natürlich vorkommende Materialien wie etwa mikroporöse Zeolithe.

Schwerpunktprogramm (SPP) 1158: Antarctic Research with Comparable Investigations in Arctic Sea Ice Areas; Bereich Infrastruktur - Antarktisforschung mit vergleichenden Untersuchungen in arktischen Eisgebieten, Investigation of mechanism driving glacial/interglacial variability in stratification/mixing and biological productivity of the Pacific Southern Ocean and potential implications on air-sea CO2-exchange: synthesis of climate and ocean biogeochemical modeling with paleoceanographic reconstructions

Atmospheric CO2 concentrations present a repetitive pattern of gradual decline and rapid increase during the last climate cycles, closely related to temperature and sea level change. During the Last Glacial Maximum (LGM; 23-19 kyr BP), when sea level was ca. 120 m below present, the ocean must have stored additionally about 750 Gt carbon. There is consensus that the Southern Ocean represents a key area governing past and present CO2 change. The latter is not only of high scientific but also of socio-economic and political concern since the Southern Ocean provides the potential for an efficient sink of anthropogenic carbon. However, the sensitivity of this carbon sink to climate-change induced reorganizations in wind patterns, ocean circulation, stratification, sea ice extent and biological production remains under debate. Models were not yet able to reproduce the necessary mechanisms involved, potentially due to a lack of the dynamic representation/resolution of atmospheric and oceanic circulation as well as missing carbon cycling. Data on past Southern Ocean hydrography and productivity are mainly from the Atlantic sector, thus do not adequately document conditions in the Pacific sector. This sector is not only the largest part of the Southern Ocean, but it also represents the main drainage area of the marine-based West Antarctic Ice Sheet (WAIS). In the proposed study we aim to generate paleo-data sets with a newly established proxy method from sediment core transects across the Pacific Southern Ocean. This will enhance the baselines for the understanding and modeling of the Southern Ocean's role in carbon cyling, i.e. ocean/atmosphere CO2 exchange and carbon sequestration. It will also allow insight into the response of the WAIS to past warmer than present conditions. Paired isotope measurements (oxygen, silicon) will be made on purified diatoms and radiolarians to describe glacial/interglacial contrasts in physical and nutrient properties at surface and subsurface water depth. This will be used to test (i) the impact of yet unconsidered dust-borne micronutrient deposition on the glacial South Pacific on shifts of primary productivity, Si-uptake rates and carbon export, (ii) the 'silicic-acid leakage' hypothesis (SALH) and (iii) the formation and extent of surface water stratification. Diatom and radiolarian oxygen isotopes will provide information on the timing of surface ocean salinity anomalies resulting from WAIS melt water. Climate model simulations using a complex coupled atmosphere ocean general circulation model (AOGCM) in combination with a sophisticated ocean biogeochemical model including Si-isotopes will be used for comparison with the paleo records. The analysis will cover spatial as well as temporal variability patterns of Southern Ocean hydrography, nutrient cycling and air-sea CO2-exchange. With the help of the climate model we aim to better separate and statistically analyse the individual impacts of ocean circulation and bio

Entwicklung eines Methanoxidationskatalysators auf Basis von biogenem Silica für die Entfernung von Methan im Abgas von Biogas-BHKW, Teilvorhaben: Entwicklung von Katalysatoren auf Basis von biogenem Silica für die Totaloxidation von Methan

Das Projekt hat die Entwicklung und Untersuchung eines hinreichend aktiven sowie langzeitstabilen Katalysators zur Oxidation von Methan im Abgas von Biogas-Blockheizkraftwerken (BHKW) zum Ziel. Die Basis dafür bildet pulverförmiges biogenes Silica, welches aus der energetischen Verwertung von biogenen Rest- und Abfallstoffen gewonnen wird. Zusammen mit den aktiven Komponenten wird dies einerseits als Washcoat auf a-Aluminiumoxid Hohlkugeln aufgebracht. Andererseits werden Hohlkugeln aus dem pulverförmigen Katalysator gefertigt. Im Projektverlauf wird die Katalysatorentwicklung ausgehend vom Labormaßstab nach Upscaling auch unter realen Bedingungen abgebildet. Die Untersuchungen sollen unter Praxisbedingungen durchgeführt werden. Dabei soll unter Verwendung einer mobilen Katalysatortestapparatur mit Realabgas und nachfolgend direkt im BHKW-Abgasstrang der Nachweis der Praxistauglichkeit geführt werden.

Seawater carbonate chemistry and mass fluxes and elemental composition of particulate export in KOSMOS mesocosm experiments (2010-2014)

Diatoms account for up to 40% of marine primary production and require silicic acid to grow and build their opal shell. On the physiological and ecological level, diatoms are thought to be resistant to, or even benefit from, ocean acidification. Yet, global-scale responses and implications for biogeochemical cycles in the future ocean remain largely unknown. Here we conducted five in situ mesocosm experiments with natural plankton communities in different biomes and find that ocean acidification increases the elemental ratio of silicon (Si) to nitrogen (N) of sinking biogenic matter by 17 ± 6 per cent under pCO2 conditions projected for the year 2100. This shift in Si:N seems to be caused by slower chemical dissolution of silica at decreasing seawater pH. We test this finding with global sediment trap data, which confirm a widespread influence of pH on Si:N in the oceanic water column. Earth system model simulations show that a future pH-driven decrease in silica dissolution of sinking material reduces the availability of silicic acid in the surface ocean, triggering a global decline of diatoms by 13–26 per cent due to ocean acidification by the year 2200. This outcome contrasts sharply with the conclusions of previous experimental studies, thereby illustrating how our current understanding of biological impacts of ocean change can be considerably altered at the global scale through unexpected feedback mechanisms in the Earth system.

Entwicklung eines Methanoxidationskatalysators auf Basis von biogenem Silica für die Entfernung von Methan im Abgas von Biogas-BHKW, Teilvorhaben: Applikation und Einführung eines umweltfreundlichen Oxidationskatalysators in die industrielle Fertigung für marktspezifische Anwendungen

Das Projekt hat die Entwicklung und Untersuchung eines hinreichend aktiven sowie langzeitstabilen Katalysators zur Oxidation von Methan im Abgas von Biogas-Blockheizkraftwerken (BHKW) zum Ziel. Die Basis dafür bildet pulverförmiges biogenes Silica, welches aus der energetischen Verwertung von biogenen Rest- und Abfallstoffen gewonnen wird. Zusammen mit den aktiven Komponenten wird dies einerseits als Washcoat auf a-Aluminiumoxid Hohlkugeln aufgebracht. Andererseits werden Hohlkugeln aus dem pulverförmigen Katalysator gefertigt. Im Projektverlauf wird die Katalysatorentwicklung ausgehend vom Labormaßstab nach Upscaling auch unter realen Bedingungen abgebildet. Die Untersuchungen sollen unter Praxisbedingungen durchgeführt werden. Dabei soll unter Verwendung einer mobilen Katalysatortestapparatur mit Realabgas und nachfolgend direkt im BHKW-Abgasstrang der Nachweis der Praxistauglichkeit geführt werden.

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