978 resultados para Peatland lakes


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Precise relative sea level (RSL) data are important for inferring regional ice sheet histories, as well as helping to validate numerical models of ice sheet evolution and glacial isostatic adjustment. Here we develop a new RSL curve for Fildes Peninsula, South Shetland Islands (SSIs), a sub-Antarctic archipelago peripheral to the northern Antarctic Peninsula ice sheet, by integrating sedimentary evidence from isolation basins with geomorphological evidence from raised beaches. This combined approach yields not only a Holocene RSL curve, but also the spatial pattern of how RSL change varied across the archipelago. The curve shows a mid-Holocene RSL highstand on Fildes Peninsula at 15.5 m above mean sea level between 8000 and 7000 cal a BP. Subsequently RSL gradually fell as a consequence of isostatic uplift in response to regional deglaciation. We propose that isostatic uplift occurred at a non-steady rate, with a temporary pause in ice retreat ca. 7200 cal a BP, leading to a short-lived RSL rise of ~1 m and forming a second peak to the mid-Holocene highstand. Two independent approaches were taken to constrain the long-term tectonic uplift rate of the SSIs at 0.22-0.48 m/ka, placing the tectonic contribution to the reconstructed RSL highstand between 1.4 and 2.9 m. Finally, we make comparisons to predictions from three global sea level models.

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List of non-indigenous species (NIS) established in the Great Lakes-St. Lawrence River region and the North and Baltic Seas region, their geographic origin, and taxonomic assignment. Asterisks mark the NIS that occur in both the North and Baltic Seas and the Great Lakes-St. Lawrence River regions. GL, SL, NW, NE, SW and SE denote the Great Lakes, St. Lawrence River, north-west, north-east, south-west, and south-east, respectively. Eurasia represents inland freshwaters except Yangtze River, Indo-Pacific represents Indian Ocean and the archipelago of Indonesia, Malaysia, and Pilipinas, North America (N America) represents inland freshwaters except the Laurentian Great Lakes, St. Lawrence and Mississippi Rivers, while Australia, New Zealand, Africa and South America (S America) cover all inland freshwaters in these areas.

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Acknowledgements BP Exploration Co. is thanked for funding, and particularly the Carbonate Team (Anna Matthews, Teresa Sabato Ceraldi, and Darryl G. Green) for supporting this research and for fruitful discussions. Mark Anderson, Kim Rosewell, and Tony Sinclair (University of Hull) are thanked for laboratory assistance, and for SEM sample preparation and set-up respectively. The technical and human support from Prof. Jörg Hardege and Maggy A. Harley (University of Hull) was key to perform these experiments. We would like to acknowledge an anonymous reviewer for the detailed and constructive comments, and Brian Jones's editorial handling of the manuscript which is greatly appreciated.

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Funding: This work was supported by the following sources of funding: European Research Council ERC (project GA 335910 VEWA) for funding through the VeWa project (DT); Leverhulme Trust for funding through PLATO (RPG-2014-016) (DT). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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The GloboLakes project, a global observatory of lake responses to environmental change, aims to exploit current satellite missions and long remote-sensing archives to synoptically study multiple lake ecosystems, assess their current condition, reconstruct past trends to system trajectories, and assess lake sensitivity to multiple drivers of change. Here we describe the selection protocol for including lakes in the global observatory based upon remote-sensing techniques and an initial pool of the largest 3721 lakes and reservoirs in the world, as listed in the Global Lakes and Wetlands Database. An 18-year-long archive of satellite data was used to create spatial and temporal filters for the identification of waterbodies that are appropriate for remote-sensing methods. Further criteria were applied and tested to ensure the candidate sites span a wide range of ecological settings and characteristics; a total 960 lakes, lagoons, and reservoirs were selected. The methodology proposed here is applicable to new generation satellites, such as the European Space Agency Sentinel-series.

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Mercury concentrations ([Hg]) in Arctic food fish often exceed guidelines for human subsistence consumption. Previous research on two food fish species, Arctic char (Salvelinus alpinus) and lake trout (Salvelinus namaycush), indicates that anadromous fish have lower [Hg] than nonanadromous fish, but there have been no intraregional comparisons. Also, no comparisons of [Hg] among anadromous (sea-run), resident (marine access but do not migrate), and landlocked (no marine access) life history types of Arctic char and lake trout have been published. Using intraregional data from 10 lakes in the West Kitikmeot area of Nunavut, Canada, we found that [Hg] varied significantly among species and life history types. Differences among species-life history types were best explained by age-at-size and C:N ratios (indicator of lipid); [Hg] was significantly and negatively related to both. At a standardized fork length of 500 mm, lake trout had significantly higher [Hg] (mean 0.17 µg/g wet wt) than Arctic char (0.09 µg/g). Anadromous and resident Arctic char had significantly lower [Hg] (each 0.04 µg/g) than landlocked Arctic char (0.19 µg/g). Anadromous lake trout had significantly lower [Hg] (0.12 µg/g) than resident lake trout (0.18 µg/g), but no significant difference in [Hg] was seen between landlocked lake trout (0.21 µg/g) and other life history types. Our results are relevant to human health assessments and consumption guidance and will inform models of Hg accumulation in Arctic fish.

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During the "Challenger" Deep-Sea Exploring Expedition a great many peculiar-looking manganese nodules or concretions were dredged from the floor of the ocean at great depths, chiefly in the Red Clay areas of the Pacific. In the present paper we propose to point out the distribution of the oxides of manganese in the geological series of rocks, in fresh and sea water, and in marine deposits, with special reference to our explorations in the lochs of the west of Scotland; to give an account of investigations undertaken to ascertain the source of the manganese present in marine deposits in the form of the higher oxides, and thereafter to discuss the various views that have been advanced to explain the formation and distribution of manganese concretions in marine deposits in general.

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Dieser Datensatz beinhaltet 70 Pollenprofile und begleitende sedimentologische Daten aus 30 Seen in Deutschland, die im Verlauf der 70er und 80er Jahre vom NlfB gekernt und analysiert wurden. Der Datenatz wurde im Rahmen des im folgenden beschriebenen Teilprojektes des DFG-Schwerpunktprogrammes "Wandel der Geo-Biosphäre" von Prof. Dr. Josef Merkt der wissenschaftlichen Gemeinschaft zur Verfügung gestellt. Im Projekt "Laminierte Seesedimente als Archive für Untersuchungen der Änderungen von Umweltbedingungen während Spätglazial und Holozän" wurden die laminierten Abschnitte von Sedimentprofilen aus oberschwäbischen, nordschweizerischen und norddeutschen Seen, die die letzten 15 000 Jahre umfassten, mikroskopisch ausgewertet. Ziel war es für Deutschland eine jahrgenaue Chronologie nach Kalenderjahren aufzustellen. Poster: Kleinmann, A, Merkt, J, Müller, H, Küster, H (1998) Holocene lake-level changes in Germany. Institute of Geobotany, University Hannover & Geological Survey of Lower Saxony, Hannover. (pdf hdl:10013/epic.31687.d001 280kB) Einführung: Die meisten Seen in Deutschland bestehen seit mehr als 15 000 Jahren und sind seit Jahrtausenden attraktiv für menschliche Besiedlung. In den Seeablagerungen ist die Geschichte der Umwelt nahezu ungestört und hoch aufgelöst konserviert. Pflanzliche und tierische Reste, wie z. B. Blütenstaub, Birkenfrüchte, Bucheckern, Algen, Wasserflöhe, Käfer, Muschelkrebse und Rädertierchen können Auskunft über die Entwicklung der Flora und Fauna, über Wärme- und Kälteperioden seit der letzten Eiszeit bis heute geben. Weitere Zeugen sind z.B. klastischer Eintrag (wie Sand), vulkanische Aschen, chemische Ausfällungen und eine jahreszeitliche Schichtung, die nur unter Sauerstoffausschluß entsteht. Ist der Seegrund belüftet, leben dort Tiere, die die oberen Zentimeter des Seebodens zur Nahrungssuche durchwühlen und dabei diese Schichtung zerstören. Ist der Seegrund ganzjährig unbelüftet, bleiben die klastischen Partikel, die organischen Reste, die chemischen Fällungen wie Siderit und Kalzit in der Reihenfolge liegen wie sie abgesunken sind. Die Reihenfolge spiegelt den Ablauf der Jahreszeiten wider: Goldalgen fallen im Frühjahr und die Mehrheit der Kieselalgen im Frühsommer und Sommer auf den Seeboden. Eisenkarbonat und Kalk werden im Sommer ausgeschieden, die klastischen und organischen Partikel sedimentieren im Winter. Die Jahresschichten liefern das zeitliche Gerüst in dem sich Klimaumschwünge, Seespiegeltiefstände und andere Ereignisse der Paläoumwelt jahrgenau fassen lassen. Auch die Landnutzung durch den Menschen ist aus Seeablagerungen abzulesen, wie z. B. erster Ackerbau, Rodungshochphasen in der Römerzeit und im Mittelalter, Aufforstung Anfang des 19. Jahrhunderts, bronzezeitliche und jüngere Erzverhüttungen, Industrialisierung, sogar Atombombentests und das Reaktorunglück von Tschernobyl 1986. Diese deuten das umwelt-wissenschaftliche Potential der Seesedimente an. Wesentliche Antworten, die in Seesedimenten stecken und entschlüsselt werden, sind die auf Fragen nach Klimaänderungen und ihren Folgen. Neben den bekannten vulkanischen Aschenlagen Laacher Tuff aus der Eifel, Saksunarvatn Tuff aus Island und Kilian/Vasset Tuff aus dem Massif Central werden weitere gesucht, da sie trennscharfe Leithorizonte sind und zur absoluten zeitlichen Korrelation von See zu See dienen. Daneben können regional unterschiedliche Vegetationsentwicklungen über isochrone Tephralagen einander zugeordnet werden. Mit der Erfassung möglichst vieler Sedimentparameter können Kriterien gefunden werden, mit denen die natürlichen von den anthropogenen Umweltveränderungen zu unterscheiden sind. Klimatisch unruhige Zeitabschnitte wie der Übergang Alleröd/Jüngere Tundrenzeit vor 12700 Kalenderjahren, der Übergang Spätglazial/Holozän vor 11560 Kalenderjahren und die 120 Jahre später einsetzende vorübergehende Abkühlung, die Rammelbeekphase, wurden analysiert, um Dauer, Verlauf und Folgeerscheinungen kennenzulernen. Als Methoden wurden eingesetzt: Mikrofaziesanalyse mit Dünnschliffen, Pollenanalyse, Mikrofaunauntersuchungen, anorganisch und organisch geochemische Analysen, Isotopenanalyse (delta13C, delta18O, AMS an terrestrischen Makroresten).

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Over the last several decades, human activities have resulted in environmental changes that have increased the number of stressors that can act on a single environment. In Canadian Shield lakes, two recent stressors, the invasion of Bythotrephes longimanus and calcium decline, have been documented. Widespread acidification of hundreds of North American lakes has resulted in the precipitous decline of lake water calcium concentration. Crustacean zooplankton with high calcium demands are likely to be vulnerable to calcium decline, especially <1.5 mg Ca/L, where survival and reproduction rates are reduced. These taxa are also vulnerable to predation by Bythotrephes that has been implicated in the loss of pelagic biodiversity in soft water lakes. Despite laboratory and field studies aimed at understanding the independent impact of these stressors, it is unclear how their co-occurrence will influence community response. Using a combination of data from a large regional lake survey and field experiments, I examined the individual and joint effects of Bythotrephes and calcium decline on native zooplankton community structure. Results demonstrated that much is known about Bythotrephes and our findings of reduced total zooplankton and species richness, due to the loss of Cladocera, are consistent with field surveys and other experimental studies. While we did not detect strong evidence for an effect of calcium on zooplankton using the lowest calcium concentration among invaded lakes (1.2 mg Ca/L), there is evidence that, as lake water calcium concentrations fall <1 mg Ca/L, per capita growth rates of a broad variety of taxa are expected to decline. At the regional scale, negative effects of Bythotrephes and calcium on abundances of small cladocerans and Daphnia pulicaria, respectively, were in agreement with my experimental observations. We also observed significant interactions between Bythotrephes and calcium for a broad variety of taxa. As Bythotrephes continues to spread and invade lakes that are also declining in aqueous calcium, both stressors are likely to amplify negative effects on Cladocera that appear the most vulnerable. Loss of these important zooplankton in response to both Bythotrephes and calcium decline, is likely to lower zooplankton productivity, with potential effects on phytoplankton and higher trophic levels.

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Recent proxy measurements reveal that subglacial lakes beneath modern ice sheets periodically store and release large volumes of water, providing an important but poorly understood influence on contemporary ice dynamics and mass balance. This is because direct observations of how lake drainage initiates and proceeds are lacking. Here we present physical evidence of the mechanism and geometry of lake drainage from the discovery of relict subglacial lakes formed during the last glaciation in Canada. These palaeo-subglacial lakes comprised shallow (<10 m) lenses of water perched behind ridges orientated transverse to ice flow. We show that lakes periodically drained through channels incised into bed substrate (canals). Canals sometimes trend into eskers that represent the depositional imprint of the last high-magnitude lake outburst. The subglacial lakes and channels are preserved on top of glacial lineations, indicating long-term re-organization of the subglacial drainage system and coupling to ice flow.

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This fact sheet summarizes the water quality data collected as part of the Iowa Department of Natural Resources ambient lake monitoring program.

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Peatland restoration involves giving aid to a complex ecosystem which has been damaged in some way. A reasonable analogy is a patient brought to a hospital for urgent treatment. When arriving at Accident & Emergency , the first priority of the medical team is to stabilise the patient’s condition. Only after the patient’s condition has been assessed and then stabilised can the team begin to think about the longer - term process of healing and recovery. A similar logic is applied to peatland s . First , stabilisation is required to prevent further degradation, following which restoration can focus on the recovery of the ecosystem.