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Results of palynological analysis from 2020 of the varved MO-05 core from Lake Mondsee (Austria) section (249-526 cm)

This study reports a precisely dated pollen record with a 20-year resolution from the varved sediments of Lake Mondsee in the north-eastern European Alps (47°49′N, 13°24′E, 481 m above sea level). The analysed part of core spans the interval between 1500 BCE and 500 CE and allows changes in vegetation composition in relation to climatic changes and human activities in the catchment to be inferred. Intervals of distinct but modest human impact are identified at ca. 1450-1220, 740-490 and 340-190 BCE and from 80 BCE to 180 CE. While the first two intervals are synchronous with prominent salt mining phases during the Bronze Age and Early Iron Age at the nearby UNESCO World Heritage Site of Hallstatt, the last two intervals fall within the Late Iron Age and Roman Imperial Era, respectively. Comparison with published records of extreme runoff events obtained from the same sediment core shows that human activities (including agriculture and logging) around Lake Mondsee were low during intervals of high flood frequency as indicated by a higher number of intercalated detrital event layers, but intensified during hydrologically stable intervals. Comparison of the pollen percentages of arboreal taxa with the stable oxygen isotope and potassium ion records of the NGRIP and GISP2 ice cores from Greenland reveals significant positive correlations for Fagus and negative correlations for Betula and Alnus. This underlines the sensitivity of vegetation around Lake Mondsee to temperature fluctuations in the North Atlantic as well as to moisture fluctuations controlled by changes in the intensity of the Siberian High and the North Atlantic Oscillation (NAO) regime.

The iron-snow regime in Fe-FeS cores: a numerical and experimental approach

In the Earth, the dynamo action is strongly linked to core freezing. There is a solid inner core, the growth of which provides a buoyancy flux that drives the dynamo. The buoyancy in this case derives from a difference in composition between the solid inner core and the fluid outer core. In planetary bodies smaller than the Earth, however, this core differentiation process may differ - Fe may precipitate at the core-mantle boundary (CMB) rather than in the center and may fall as iron snow and initially remelt with greater depth. A chemical stable sedimentation zone develops that comprises with time the entire core - at that time a solid inner core starts to grow. The dynamics of this system is not well understood and also whether it can generate a magnetic field or not. The Jovian moon Ganymede, which shows a present-day magnetic dipole field, is a candidate for which such a scenario has been suggested. We plan to study this Fe-snow regime with both a numerical and experimental approach. In the numerical study, we use a 2D/3D thermo-chemical convection model that considers crystallization and sinking of iron crystals together with the dynamics of the liquid core phase (for the 3D case the influence of the rotation of the Fe snow process is further studied).The numerical calculations will be complemented by two series of experiments: (1) investigations in metal alloys by means of X-ray radioscopy, and (2) measurements in transparent analogues by optical techniques. The experiments will examine typical features of the iron snow regime. On the one hand they will serve as a tool to validate the numerical approach and on the other hand they will yield important insight into sub-processes of the iron snow regime, which cannot be accessed within the numerical approach due to their complexity.

Stable isotope and hydrochemical composition of fresh water in rivers of the Basin of Pöhlde, and the Rhume karst springs, Germany, under different seasonal and discharge conditions

The hydrochemical and stable isotope composition of fresh surface water in rivers (Sieber and Oder) of a karst area in the southwestern foreland of the Harz Mountains, Germany, was investigated at several occasions between years 1986 and 1992. The campaigns covered different seasonal and hydrological (discharge) conditions, including a snow-melt induced high water at the rivers. Aim of the study was the investigation of the impact of discharge conditions at the river water loosing water to underground passage in the Basin of Pöhlde, dissolving carbonate and sulfate minerals in the karst aquifers, and reappearing in the karst springs of the Rhume river. Besides physical characterization, hydrochemical major and minor elements were measaured, as weill as the carbon isotope composition of DIC, the sulfur and oxygen isotope composition of sulfate, and the oxygen isotope composition of water. Results reflect the impact of hydrological conditions on the subterrestrial carbon and sulfur cycles.

Seasonal Dataset of DIC, δ13CDIC, DOC, δ13CDOC, pCO2(aq), FCO2 and Biogeochemical Parameters in the Danube River (2023–2024)

This dataset contains dissolved inorganic/organic carbon (DIC/DOC) concentrations, its stable isotope ratios (δ13CDIC/DOC), partial pressure of carbon dioxide in the water column pCO₂(aq) (pCO2(aq)) and area-integrated CO₂ emission rates derived from flux calculations (FCO2; g C d⁻¹), along with corresponding parameters (temperature, pH, calcium, bicarbonate) collected from the Danube River and its key tributaries during five seasonal sampling campaigns in 2023 and 2024. Water samples were collected using a weighted 2 L sampling bottle submerged 1–2 meters below the surface, with sampling conducted from the river center via bridges or passenger boats, and occasionally from the riverbank. In situ temperature measurements were taken with a multiparameter instrument (HQ40d, HACH™, Loveland, CO, USA). δ13ODIC/DOC was analyzed using a OI Analytical Aurora 1030W-IRMS. This dataset is providing valuable insights into carbon dynamics in a large river system and support investigations of biogeochemical cycling. It further can inform ecosystem management and conservation strategies under changing environmental conditions.

Forschergruppe (FOR) 861: Cross-scale Monitoring: Biodiversity and Ecosystem Functions, Quantification of functional hydro-biogeochemical indicators in Ecuadorian ecosystems and their reaction on global change

Water is an intrinsic component of ecosystems acting as a key agent of lateral transport for particulate and dissolved nutrients, forcing energy transfers, triggering erosion, and driving biodiversity patterns. Given the drastic impact of land use and climate change on any of these components and the vulnerability of Ecuadorian ecosystems with regard to this global change, indicators are required that not merely describe the structural condition of ecosystems, but rather capture the functional relations and processes. This project aims at investigating a set of such functional indicators from the fields of hydrology and biogeochemistry. In particular we will investigate (1) flow regime and timing, (2) nutrient cycling and flux rates, and (3) sediment fluxes as likely indicators. For assessing flow regime and timing we will concentrate on studying stable water isotopes to estimate mean transit time distributions that are likely to be impacted by changes in rainfall patterns and land use. Hysteresis loops of nitrate concentrations and calculated flux rates will be used as functional indicators for nutrient fluxes, most likely to be altered by changes in temperature as well as by land use and management. Finally, sediment fluxes will be measured to indicate surface runoff contribution to total discharge, mainly influenced by intensity of rainfall as well as land use. Monitoring of (1) will be based on intensive sampling campaigns of stable water isotopes in stream water and precipitation, while for (2) and (3) we plan to install automatic, high temporal-resolution field analytical instruments. Based on the data obtained by this intensive, bust cost effective monitoring, we will develop the functional indicators. This also provides a solid database for process-based model development. Models that are able to simulate these indicators are needed to enable projections into the future and to investigate the resilience of Ecuadorian landscape to global change. For the intended model set up we will couple the Catchment Modeling Framework, the biogeochemical LandscapeDNDC model and semi-empirical models for aquatic diversity. Global change scenarios will then be analyzed to capture the likely reaction of functional indicators. Finally, we will contribute to the written guidelines for developing a comprehensive monitoring program for biodiversity and ecosystem functions. Right from the beginning we will cooperate with four SENESCYT companion projects and three local non-university partners to ensure that the developed monitoring program will be appreciated by locals and stakeholders. Monitoring and modelling will focus on all three research areas in the Páramo (Cajas National Park), the dry forest (Reserva Laipuna) and the tropical montane cloud forest (Reserva Biologica San Francisco).

INSPIRE SN Landwirtschaftliche Anlagen und Aquakulturanlagen

Der Datensatz beinhaltet Informationen zu Landwirtschaftlichen Anlagen im Freistaat Sachsen. Dargestellt werden Daten zu Tierhaltungsanlagen.

Tripelelement-Stabilisotopensignaturen zur Untersuchung des atmosphärischen Chlormethanbudgets

Die stratosphärische Ozonschicht absorbiert die UV-C und UV-B Sonnenstrahlung und schützt damit Pflanzen, Tiere und Menschen vor Strahlenschäden. Durch anthropogen emittierte Fluorchlorkohlenwasserstoffe (FCKWs) wird die Ozonschicht abgebaut. Da FCKWs seit dem Montrealer Protokoll stark zurückgegangen sind, werden halogenierte Verbindungen wie Chlormethan (CH3Cl), die aus natürlichen Quellen freigesetzt werden, für den Abbau der Ozonschicht in der Stratosphäre zunehmend relevant. CH3Cl ist das am häufigsten vorkommende chlorhaltige Spurengas in der Erdatmosphäre, das für etwa 17% der durch Chlor katalysierten Ozonzerstörung in der Stratosphäre verantwortlich ist. Daher wird CH3Cl vornehmlich die zukünftigen Gehalte an stratosphärischem Chlor bestimmen. Die aktuellen Schätzungen des globalen CH3Cl-Budgets und die Verteilung der Quellen und Senken sind sehr unsicher. Ein besseres Verständnis des atmosphärischen CH3Cl-Budgets ist daher das Hauptziel dieses Projektes.Die Analyse stabiler Isotopenverhältnisse von Wasserstoff (H), Kohlenstoff (C) und Chlor (Cl) hat sich zu einem wichtigen Werkzeug zur Untersuchung des atmosphärischen CH3Cl-Budgets entwickelt. Das zugrundeliegende Konzept besteht darin, dass das atmosphärische Isotopenverhältnis einer Verbindung wie CH3Cl gleich der Summe der Isotopenflüsse aus allen Quellen angesehen werden kann, korrigiert um den gewichteten durchschnittlichen kinetischen Isotopeneffekt aller Abbauprozesse. Dadurch ist es möglich, die Bedeutung wichtiger Quellen und Senken mit bekannten Isotopensignaturen zu entschlüsseln. Eine Grundvoraussetzung für detaillierte Hochrechnungen des globalen Budgets ist die Bestimmung der durchschnittlichen Isotopenverhältnisse von H, C und Cl des troposphärischen CH3Cl. Aufgrund der relativ geringen Konzentration von atmosphärischem CH3Cl von ~550 ppbv stellt dies eine große messtechnische Herausforderung dar. Daher liegt der Schwerpunkt dieses Antrags auf der erfolgreichen Entwicklung von Dreifachelement-Isotopenmethoden zur genauen Messung von atmosphärischem CH3Cl.Im ersten Schritt wird ein Probenahmesystem für große Luftmengen konstruiert und für die Messungen der stabilen Isotopenverhältnisse von CH3Cl optimiert. Das Probenahmegerät wird zunächst im Labor getestet und dann zum Sammeln von Luftproben an drei verschiedenen Orten eingesetzt: an der Universität Heidelberg, am Hohenpeißenberg und im Schneefernerhaus. Die Probenahmen werden über einen Zeitraum von einem Jahr durchgeführt, um möglichst auch saisonale Schwankungen zu erfassen. Die Isotopenverhältnisse der Proben werden mit modernsten massenspektrometrischen Methoden im Labor gemessen. Die Ergebnisse aller Standorte und Zeitpunkte werden in der Gesamtheit evaluiert, um die durchschnittlichen stabilen H-, C und Cl-Isotopenwerte einschließlich ihrer saisonalen Schwankungen darzustellen. Abschließend werden die Daten hinsichtlich ihrer Anwendbarkeit für komplexe numerische Modelle kritisch diskutiert.

Seasonal water isotope values in eastern German lakes and rivers (Spree, Dahme, Elster and Mulde systems) in March, July, October 2022, and March 2023

Water isotopes (δ²H and δ¹⁸O) were analyzed in samples from lakes and rivers in eastern Germany. This sub-dataset is derived from water samples collected from lake and river shores. Seasonal samples were collected in March, July, October 2022, and in March 2023, with a plastic syringe from 20-50 cm depth below water surface and directly filtered and transferred into a measurement vial. Stable isotope analysis was conducted at IGB Berlin, using a Picarro L2130-i cavity ring-down spectrometer. Measurement uncertainty was quantified to <0.5 ‰ for δ²H and <0.2 ‰ for δ¹⁸O. Water chemical parameters were determined in-situ with a portable WTW-multiparameter probe. The data give information about the seasonal isotope amplitude at the sampled spots and about spatial isotope variability in different branches of the associated river systems.

Water isotope values in shore samples collected in March and July 2020 from northeastern German lake systems

Water isotopes (δ2H and δ18O) were analyzed in samples collected in lakes associated to major riverine systems in northeastern Germany throughout 2020. This sub-dataset is derived from water samples collected from lake shores. Samples were taken in March and July 2020 with a pipette from 40-60 cm depth below water surface and directly transferred into a measurement vial. Stable isotope analysis was conducted at IGB Berlin, using a Picarro L2130-i cavity ring-down spectrometer. The data give information about the seasonal isotope amplitude in the sampled lakes and about spatial isotope variability in different branches of the associated riverine systems.

RUBIN - PhoTech - VP3 biogene & industrielle Luft, TP3.2: Photonischer Abbau biogener und industrieller Schadstoffe mittels Photokatalyse

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